CN109666165A

CN109666165A - A kind of energy-absorbing method based on dynamic aggregation compositions

Info

Publication number: CN109666165A
Application number: CN201710967677.6A
Authority: CN
Inventors: 不公告发明人
Original assignee: Weng Qiumei
Current assignee: Weng Qiumei
Priority date: 2017-10-17
Filing date: 2017-10-17
Publication date: 2019-04-23

Abstract

The invention discloses a kind of energy-absorbing methods based on dynamic aggregation compositions, provide a kind of dynamic aggregation compositions and the progress energy-absorbing using it as energy-absorbing material, wherein the dynamic aggregation compositions include at least two component of A, B；Wherein, component A is the dynamic aggregation object comprising at least one cross-linked network, contains the unsaturated triple carbon-carbon bonds that alkynes cross metathesis metathesis reaction can occur and can optionally form the hydrogen bond group of supermolecule hydrogen bond action；Component B is the catalyst and/or its compound of the dynamic covalent bond generation exchange reaction in catalyst component A.The composition is used as energy-absorbing material can provide the functions such as good shock resistance (protection), damping, damping, buffering, sound insulation, noise elimination, simultaneously with optional supermolecule hydrogen bond collective effect, the characteristics such as material stimulating responsive, self-repairability, recuperability, repeatable processability are assigned, can be applied to the various aspects of daily life Yu each professional domain.

Description

A kind of energy-absorbing method based on dynamic aggregation compositions

Technical field

The present invention relates to a kind of energy-absorbing methods, and in particular to a kind of based on the dynamic aggregation object comprising at least two component of A, B The energy-absorbing method of composition.

Background technique

In the activity such as daily life, movement, amusement and recreation, military affairs, police service, security, medical care, production, human body, animal body Seriously affecting for the physical impacts such as shock, vibration, vibration, explosion, sound is often subject to article etc..By using energy-absorbing material Energy-absorbing is carried out, effective protection can be played to this kind of physical impact, is alleviated, to reach such as shock resistance, damping, damping, delay Punching, sound insulation, noise elimination and other effects.At this stage, mainly there are metal, polymer, composite material etc. for the material of energy-absorbing.It is a kind of common Polymer material energy-absorbing mechanism be cracked using the fracture and material internal of the chemical bonds such as covalent bond even material The processes energy-absorbings such as whole fracture.However during above-mentioned each, fracture and the crackle of macroscopic view, the fracture of covalent bond will lead to material The energy absorption ability and mechanical property of material are all reduced or even can not be continued to use, after primary or a small number of endergonic process several times, material Must replace in time could maintain original performance.

Therefore, it is necessary to develop the new energy-absorbing method of one kind can both embody excellent suction on the basis of the energy-absorbing mechanism Can effect, and can to avoid material because energy-absorbing be broken due to global failure, to solve problems of the prior art.

Summary of the invention

For above-mentioned background, in order to make polymer material that can not only embody excellent energy-absorbing effect, but also can be to avoid material Global failure due to energy-absorbing fracture, the present invention provides a kind of energy-absorbing methods based on dynamic aggregation compositions.For this purpose, we Dynamic covalent bond is introduced in the polymer, replaces traditional chemical covalent to be crosslinked with dynamic covalent cross-linking.Dynamic covalent cross-linking can Selfreparing is carried out to material after material is broken, not only maintains the structure and mechanical property of polymer, and prior It has been to confer to the ability that polymer can be repeated as many times energy-absorbing.Optional supermolecule hydrogen bond crosslinks, reversible breaking property is not still Enhancing to energy-absorbing effect can also further increase crosslink density, the stability and mechanical property of reinforcing material；Meanwhile it is super Molecule hydrogen bond provides dynamic, and the self-repairability of polymer also can be enhanced.

The present invention is achieved by following technical solution:

A kind of energy-absorbing method based on dynamic aggregation compositions, which is characterized in that a kind of dynamic aggregation object combination is provided Object simultaneously carries out energy-absorbing using it as energy-absorbing material, wherein the dynamic aggregation compositions include at least two component of A, B；Its In, the dynamic aggregation compositions component A is the dynamic aggregation object comprising at least one cross-linked network, and the dynamic is poly- It closes in object containing the unsaturated triple carbon-carbon bonds that alkynes cross metathesis metathesis reaction can occur；The wherein dynamic aggregation object group Polymer component B is that alkynes cross metathesis occurs for the unsaturated triple carbon-carbon bonds in the catalysis dynamic aggregation compositions component A Catalyst, catalyst composites or the catalyst of metathesis reaction and the mixture of catalyst composites；Wherein, described to send out The unsaturated triple carbon-carbon bonds of raw alkynes cross metathesis metathesis reaction have the structure being shown below:

Wherein,Indicate the connection with polymer chain or any other suitable group or atom.

In one embodiment of the invention, wherein at least one glass of the dynamic aggregation compositions component A Glass transition temperature is not higher than 25 DEG C.

In one embodiment of the invention, wherein at least one glass of the dynamic aggregation compositions component A Glass transition temperature is not higher than 0 DEG C.

In one embodiment of the invention, wherein the dynamic aggregation compositions component A all vitrifyings Transition temperature is no greater than 25 DEG C.

In one embodiment of the invention, wherein the dynamic aggregation compositions component A all vitrifyings Transition temperature is no greater than 0 DEG C.

In one embodiment of the invention, wherein at least one glass of the dynamic aggregation compositions component A Glass transition temperature is not less than 40 DEG C.

In one embodiment of the invention, wherein at least one glass of the dynamic aggregation compositions component A Glass transition temperature is not less than 100 DEG C.

In one embodiment of the invention, wherein the dynamic aggregation compositions component A all vitrifyings Transition temperature is all not less than 40 DEG C.

In one embodiment of the invention, wherein the dynamic aggregation compositions component A all vitrifyings Transition temperature is all not less than 100 DEG C.

In one embodiment of the invention, wherein at least one glass of the dynamic aggregation compositions component A Glass transition temperature is higher than 25 DEG C and is lower than 40 DEG C.

In one embodiment of the invention, wherein at least one glass of the dynamic aggregation compositions component A Glass transition temperature is not higher than 25 DEG C, and at least one glass transition temperature is not less than 100 DEG C.

In one embodiment of the invention, wherein supermolecule hydrogen bond can be formed by also containing in the dynamic aggregation object The hydrogen bond group of effect.

In one embodiment of the invention, wherein only one friendship in the dynamic aggregation compositions component A It networks network, dynamic covalent cross-linking is only contained in the cross-linked network, the degree of cross linking reaches its gel point or more.

In one embodiment of the invention, wherein only one friendship in the dynamic aggregation compositions component A It networks network, is crosslinked simultaneously containing dynamic covalent cross-linking and supermolecule in the cross-linked network, wherein the degree of cross linking of dynamic covalent cross-linking Reach its gel point or more, the degree of cross linking of supermolecule crosslinking is in its gel point above and below.

In one embodiment of the invention, wherein only one friendship in the dynamic aggregation compositions component A It networks network, is crosslinked simultaneously containing dynamic covalent cross-linking and supermolecule in the cross-linked network, wherein the degree of cross linking of dynamic covalent cross-linking In its gel point hereinafter, the degree of cross linking of supermolecule crosslinking is more than its gel point.

In one embodiment of the invention, wherein only one friendship in the dynamic aggregation compositions component A It networks network, is crosslinked simultaneously containing dynamic covalent cross-linking and supermolecule in the cross-linked network, wherein the degree of cross linking of dynamic covalent cross-linking In its gel point hereinafter, supermolecule crosslinking the degree of cross linking in its gel point hereinafter, but the sum of the two degree of cross linking more than gel point.

In one embodiment of the invention, wherein containing there are two nets in the dynamic aggregation compositions component A Network；Dynamic covalent cross-linking is contained only in 1st network, the degree of cross linking is more than its gel point；Supermolecule crosslinking is contained only in 2nd network, Its degree of cross linking is more than its gel point.

In one embodiment of the invention, wherein containing there are two nets in the dynamic aggregation compositions component A Network；Covalent cross-linking containing dynamic and supermolecule are crosslinked in 1st network, contain dynamic covalent cross-linking and oversubscription in the cross-linked network simultaneously Son crosslinking, wherein the degree of cross linking of dynamic covalent cross-linking more than its gel point, supermolecule crosslinking the degree of cross linking its gel point with It is upper or following；Supermolecule crosslinking is contained only in 2nd network, the degree of cross linking is more than its gel point.

In one embodiment of the invention, wherein containing a net in the dynamic aggregation compositions component A Network, wherein the supermolecule degree of cross linking is in the supermolecule polymerization below of its gel point only containing dynamic covalent cross-linking more than gel point Object is dispersed in dynamic covalent cross-linking network；

In one embodiment of the invention, wherein containing a net in the dynamic aggregation compositions component A Network is crosslinked containing dynamic covalent cross-linking and supermolecule in the cross-linked network, wherein the degree of cross linking of dynamic covalent cross-linking reaches simultaneously More than its gel point, the degree of cross linking of supermolecule crosslinking is in its gel point above and below；The supermolecule degree of cross linking its gel point with Under supermolecule polymer be dispersed in dynamic covalent cross-linking network.

In one embodiment of the invention, wherein containing a net in the dynamic aggregation compositions component A Network, wherein only containing dynamic covalent cross-linking more than gel point, supermolecule polymerization of the supermolecule degree of cross linking more than its gel point Object is dispersed in dynamic covalent cross-linking network with graininess.

In one embodiment of the invention, wherein containing a net in the dynamic aggregation compositions component A Network is crosslinked containing dynamic covalent cross-linking and supermolecule in the cross-linked network, wherein the degree of cross linking of dynamic covalent cross-linking reaches simultaneously More than its gel point, the degree of cross linking of supermolecule crosslinking is in its gel point above and below；The supermolecule degree of cross linking its gel point with On supermolecule polymer be dispersed in dynamic covalent cross-linking network with graininess.

In one embodiment of the invention, wherein at least a kind of hydrogen bond group is located at institute in the hydrogen bond group The side group or side chain or side group and side chain for the dynamic aggregation object stated.

In one embodiment of the invention, wherein at least a kind of hydrogen bond group contains simultaneously in the hydrogen bond group Have hydrogen bond donor and hydrogen bond receptor, wherein the hydrogen bond group for containing hydrogen bond donor and hydrogen bond receptor while described preferably comprise to A few secondary amino group；

Wherein, when containing the hydrogen bond group of hydrogen bond donor and hydrogen bond receptor when described while and being located at side group and/or end group, At least one of its further preferably following constituent:

Wherein,Indicate the connection with polymer chain, G is end group；It can be cyclic or not cyclic with G；X is respectively only It is vertical to be selected from oxygen atom or sulphur atom；

Wherein, the hydrogen bond group for containing hydrogen bond donor and hydrogen bond receptor when described while is located at main chain and/or side chain bone When frame, at least one of further preferably following constituent:

Wherein,Indicate the connection with polymer chain.

In one embodiment of the invention, wherein the hydrogen bond group is selected from carbamate groups, urea groups, thio Carbamate groups and the derivative of the above group etc..

In one embodiment of the invention, wherein the dynamic aggregation object contains at least one four teeth that are no more than Hydrogen bond group.

In one embodiment of the invention, wherein the dynamic aggregation object contains two or more hydrogen bond base Group.

In one embodiment of the invention, wherein for connecting dynamic covalent bond and dynamic covalent bond, dynamic covalently At least one of polymer segment of key and hydrogen bond group, hydrogen bond group and hydrogen bond group is that main chain is carbon-chain structure or carbon heterochain The polymer segment of structure.

In one embodiment of the invention, wherein for connecting dynamic covalent bond and dynamic covalent bond, dynamic covalently At least one of polymer segment of key and hydrogen bond group, hydrogen bond group and hydrogen bond group is that main chain is the poly- of element heterochain structure Polymer segments.

In one embodiment of the invention, wherein for connecting dynamic covalent bond and dynamic covalent bond, dynamic covalently At least one of polymer segment of key and hydrogen bond group, hydrogen bond group and hydrogen bond group is that glass transition temperature is not higher than 25 DEG C polymer segment.

In one embodiment of the invention, wherein for connecting dynamic covalent bond and dynamic covalent bond, dynamic covalently At least one of polymer segment of key and hydrogen bond group, hydrogen bond group and hydrogen bond group is that glass transition temperature is not higher than 0 DEG C polymer segment.

In one embodiment of the invention, wherein for connecting dynamic covalent bond and dynamic covalent bond, dynamic covalently At least one of polymer segment of key and hydrogen bond group, hydrogen bond group and hydrogen bond group is that glass transition temperature is not less than 40 DEG C polymer segment.

In one embodiment of the invention, wherein for connecting dynamic covalent bond and dynamic covalent bond, dynamic covalently At least one of key and the polymer segment of hydrogen bond group, hydrogen bond group and hydrogen bond group are not less than for glass transition temperature 100 DEG C of polymer segment.

In one embodiment of the invention, wherein for connecting dynamic covalent bond and dynamic covalent bond, dynamic covalently At least one of polymer segment of key and hydrogen bond group, hydrogen bond group and hydrogen bond group is that glass transition temperature is higher than 25 DEG C And the polymer segment lower than 40 DEG C.

In one embodiment of the invention, wherein for connecting dynamic covalent bond and dynamic covalent bond, dynamic covalently At least one of polymer segment of key and hydrogen bond group, hydrogen bond group and hydrogen bond group is that glass transition temperature is not higher than 25 DEG C polymer segment, and at least one be not less than 100 DEG C of polymer segment for glass transition temperature.

In one embodiment of the invention, the dynamic aggregation compositions have following any character: common Solid, elastomer, gel, foam.

In one embodiment of the invention, it further includes following for constituting the recipe ingredient of the dynamic aggregation compositions It is any or appoint it is several can additive or usable object: other polymers, auxiliary agent, filler, sweller.Wherein, other described Polymer preferably is selected from following any or appoints several: natural polymer, synthetic macromolecular compound；The auxiliary agent is excellent Selected from it is following any or appoint it is several: catalyst, initiator, antioxidant, light stabilizer, heat stabilizer, dispersing agent, emulsification Agent, fire retardant, toughener, coupling agent, solvent, lubricant, release agent, plasticizer, thickener, thixotropic agent, levelling agent, coloring Agent, fluorescent whitening agent, delustering agent, antistatic agent, dehydrating agent, biocide mildewcide, foaming agent, blowing promotor, nucleating agent, rheology Agent；The filler preferably is selected from following any or appoints several: inorganic non-metallic filler, metal packing, organic filler；Described Sweller is selected from following any or appoints several: water, organic solvent, ionic liquid, oligomer, plasticizer.

In one embodiment of the invention, the energy-absorbing method is applied to defense of resistance to impact, damping, damping, delays Punching, explosion-proof, shellproof, sound insulation, noise elimination.

Compared with prior art, the invention has the following advantages:

(1) in the energy-absorbing method provided by the invention based on dynamic aggregation compositions, when dynamic aggregation compositions In energy-absorbing application by external force and inside cracks or after being broken, utilizes the dynamic of dynamic covalent bond and optional hydrogen bond Property material self-repairability may be implemented, without replacement, use can be continued cycling through, can satisfy growing to new material Ecological requirements, this it is existing with polymeric system carry out energy-absorbing method in cannot achieve.

(2) in the energy-absorbing method provided by the invention based on dynamic aggregation compositions, used dynamic covalent bond It is based on the unsaturated triple carbon-carbon bonds that alkynes cross metathesis metathesis reaction can occur.Under the conditions of non-dynamic, triple carbon-carbon bonds Stability is high, is conducive to the stability for keeping polymer material.The reaction characteristics of alkynes cross metathesis metathesis reaction are instead Answer the crosslink density of front and back polymer network constant, this characteristic can make the topological structure of polymer network remain unchanged, and make Material property maintains to stablize.Moreover, selectable catalyst be also it is diversified, reasonably selecting different catalyst can adjust It saves dynamic covalent bond and embodies dynamic and temperature, the pH value of self-repairability etc..Further, since unsaturated triple carbon-carbon bonds (alkynyl) With certain reactivity, polymer material and product after molding still remain that further progress is modified or functionalization May, expand the application range that energy-absorbing is carried out with the grade materials.

(3) in the energy-absorbing method provided by the invention based on dynamic aggregation compositions, also selectively there is oversubscription Sub- hydrogen bond action.When polymer is by external impacts, strain-responsive can occur for dynamic supermolecule hydrogen bond, in molecular scale Upper degree of cross linking transient state increases, so that flexible and rigid transition occur, can impact energy effectively dispersed；And when polymerization Object when the external impacts being subject to are sufficiently large, supermolecule hydrogen bond action due to dynamic and weaker bond energy, can with Key-shaped formula can be sacrificed to occur to dissociate and dissipation impact energy, the range to energy absorption is expanded, it is poly- further to enrich dynamic The energy-absorbing mechanism of polymer composition.

(4) energy-absorbing method provided by the invention based on dynamic aggregation compositions has good Modulatory character.For example, Supermolecule hydrogen bond and dynamic covalent bond are combined, by parameters such as molecular structure, the molecular weight of control raw material, can prepare and provide There is the adjustable dynamic aggregation object of different appearance features, performance for energy-absorbing；For another example, pass through the position of control hydrogen bond group, type And number, dynamic reversibility dynamic aggregation object of different strengths and weaknesses can be prepared, is dissociated under different stress conditions, is realized The effect of multiple energy-absorbing.By controlling the ratio of both dynamic covalent cross-linking and supermolecule hydrogen bond crosslinks ingredient, make described surpass Molecule hydrogen bond crosslinks both can form cross-linked network in the same network jointly with dynamic covalent cross-linking, can also be individually formed Supermolecule dynamic crosslinking network, can also be individually formed the particle of supermolecule dynamic crosslinking, can also be with noncrosslinking supermolecule The form of polymer be dispersed in dynamic covalent cross-linking network or supermolecule crosslinking with dynamic covalent cross-linking be respectively formed interpenetrating or Two Semi-IPN networks etc., different structures can achieve different energy-absorbing effects.In addition, when two networks all contain oversubscription When son crosslinking, the supermolecule crosslinking that can use in two networks provides collaboration or orthogonal dynamic to adjust energy-absorbing range.

(5) compared to other existing energy-absorbing methods, the present invention is also fully utilized by dynamic covalently in addition to energy absorption performance Other characteristics of key, optional supermolecule hydrogen bond and polymer can provide mechanical strength, self-repairability, shape memory, multiple Other diversified performances such as responsiveness.In addition, other function can also be added according to actual needs in material preparation process Property additive is modified dynamic aggregation compositions material, meets extensive energy-absorbing requirement to a greater extent.

With reference to following embodiments explanation, embodiment and the appended claims, these and other features of the invention with And advantage will become obvious.

Specific embodiment

The present invention relates to a kind of methods of energy-absorbing, other are characterized in that, provide a kind of dynamic aggregation compositions simultaneously Carry out energy-absorbing using it as energy-absorbing material, the dynamic aggregation compositions include at least two component of A, B, component A be comprising The dynamic aggregation object of at least one cross-linked network, it is anti-containing alkynes cross metathesis double decomposition can occur in the dynamic aggregation object The hydrogen bond group of supermolecule hydrogen bond action can be formed existing for the unsaturated triple carbon-carbon bonds and selectivity answered；Component B is catalysis group The catalyst and/or its compound of alkynes cross metathesis metathesis reaction occur for the unsaturated triple carbon-carbon bonds divided in A.

Term " energy-absorbing " used refers to for caused by the forms such as shock, vibration, vibration, explosion, sound in the present invention Physical impact absorption, dissipation and the dispersion of the energy that generate, but do not include the only absorption to thermal energy and/or electric energy, to reach To such as shock resistance (protection), damping, damping, buffering, sound insulation, noise elimination and other effects.

In order to illustrate simplicity the term is indicated using conjunction "and/or" in the description of the invention It may include the option selected from the conjunction "and/or" foregoing description, or described option after conjunction "and/or", Or it is simultaneously selected from described these three situations of option before and after conjunction "and/or".

In the following, first being carried out specifically to the dynamic aggregation compositions component A (hereinafter referred to as " component A ") in the present invention It is bright.

Heretofore described " polymerization " reaction/action be chain propagation process/effect, namely by intermolecular reaction/ Effect (including covalent chemical reaction and supermolecule hydrogen bond action) formation straight chain, branching, ring, two-dimensional/three-dimensional cluster, three-dimensional are unlimited The polymer of network structure.

Term " crosslinking " reaction/action used in the present invention, refer to intermolecular and/or intramolecular by covalent bond and/ Or supermolecule hydrogen bond action forms the process with three-dimensional unlimited reticular pattern product.In cross-linking process, polymer chain is generally first Constantly increase in two-dimensional/three-dimensional direction, gradually form cluster (can be two dimension or three-dimensional), developing deeply is three-dimensional infinite net Network.Therefore, crosslinking can be considered as a kind of special shape of polymerization.In cross-linking process, just reach a three-dimensional infinite network When the degree of cross linking, referred to as gel point, also referred to as percolation threshold.The cross-linking products (contained, similarly hereinafter) more than gel point, have Three-dimensional infinite network structure, cross-linked network constitute an entirety and across entire polymer architectures；In gel point friendship below Co-product, is only lax interchain link structure, and not formed three-dimensional infinite network structure, and is not belonging to across entire polymerization The cross-linked network that can constitute an entirety of object structure.Unless stated otherwise, the present invention in cross-linked structure be gel point with On three-dimensional infinite network structure, non-crosslinking structure includes the line style that the degree of cross linking is zero and non-linearity structure and gel point or less Two-dimensional/three-dimensional cluster structure.

In the present invention, " skeleton " refers to structure on the chain length direction of polymer chain.It is described for cross-linked polymer " main chain ", refer to any segment being present in cross-linked network skeleton.It is described for the polymer of non-crosslinking structure " main chain " refers to the most chain of chain link if not otherwise indicated.Wherein, " side chain " refers to same main polymer chain phase Connect and be distributed in the chain structure of main chain side；Wherein, " branch "/" bifurcated chain " can be side chain and be also possible to other The chain structure come out from any chain bifurcated.Wherein, " side group " refers to that any chain of same polymer is connected and is distributed in The chemical group of chain side.Wherein, " end group " refers to that any chain of same polymer is connected and is located at the change of chain end Learn group.If not otherwise indicated, side group refers in particular to group of the molecular weight no more than 1000Da for being connected to polymer chain skeleton side And subunit group therein.When the molecular weight of side chain, branch, bifurcated chain is no more than 1000Da, itself and group thereon are regarded For side group.If not otherwise indicated, side chain, branch, bifurcated chain are collectively referred to as side chain.Above-mentioned " side chain ", " side group ", can have more Level structure namely side chain/side group can continue with side chain/side group, side chain/side group side chain/side group can continue to have side chain/ Side group.In the present invention, if not otherwise indicated, for hyperbranched and dendroid chain and its relevant chain structure, the polymerization of outermost Object segment can be considered as side chain, and rest part can be considered as main chain.

Heretofore described " dynamic covalent cross-linking network " is referred to when supermolecular mechanism is all disconnected in covalent cross-linking network It opens when only remaining common covalent bond and dynamic covalent bond, still with the polymer network of the above structure of gel point；And when dynamic is total When valence link also all disconnects, original crosslinked polymer network dissociation resolves into following any or appoints several secondary units: monomer gathers Close object chain segment, polymer cluster, polymer beads more than gel point etc..

Heretofore described " supermolecule cross-linked network " refers to all disconnecting only when the dynamic covalent bond in cross-linked network When remaining common covalent bond and supermolecule hydrogen bond, still with the polymer network of the above structure of gel point；And work as supermolecule hydrogen bond When also all disconnecting, following any or several secondary units: monomer, polymer are resolved into original crosslinked polymer network dissociation Chain segment, polymer cluster, polymer beads more than gel point etc..

Heretofore described " common covalent bond ", what is referred to is traditional covalent in addition to dynamic covalent bond Key, under typical temperature (is generally not more than 100 DEG C) and (generally less than 1 day) is more difficult in the usual time is broken comprising But it is not limited only to common carbon-carbon bond, carbon-oxygen bond, carbon-hydrogen link, carbon-nitrogen bond, carbon-sulfide linkage, nitrogen-hydrogen bond, nitrogen-oxygen key, hydrogen-oxygen Key, nitrogen-nitrogen key etc..

Heretofore described " dynamic covalent bond ", refers to the unsaturated carbon carbon that alkynes cross metathesis metathesis reaction can occur Three keys (hereinafter referred to as " triple carbon-carbon bonds ").Wherein, " the alkynes cross metathesis metathesis reaction " refers to by metal alkynes Carbon skeleton rearrangement reaction between the triple carbon-carbon bonds of complex catalysis.Wherein, described " rearrangement reaction " refers to that new triple carbon-carbon bonds exist Elsewhere generates and dissociates with old triple carbon-carbon bonds, to generate the exchange of chain and the change of polymer local topology Change.For the purpose of the present invention, in this rearrangement process, due to the particularity of reaction, the crosslink density of polymer network is basically unchanged. Wherein, described " can occur " refers to, in the presence of a suitable catalyst, when temperature condition, pressure condition, alkynes intersects easy Position metathesis reaction can carry out.

Heretofore described " supermolecular mechanism " refers to supermolecule hydrogen bond action, referred to as " hydrogen bond action " or " hydrogen bond ".

In embodiments of the present invention, the component A can not have glass transition temperature, can have one Or more than one glass transition temperature.Wherein, a kind of preferred embodiment is at least one glass transition of component A Temperature is not higher than 25 DEG C, more preferably not above 0 DEG C, more preferably glass transition temperature all when there are multiple glass transition temperatures 25 DEG C are not higher than, most preferably all glass transition temperatures are not higher than 0 DEG C, help to embody supermolecule hydrogen bond in room temperature and low Dynamic and self-repairability, the materials such as readily available adhesive, elastomer, gel or product when temperature uses；It is another preferred Embodiment be component A at least one glass transition temperature be not less than 40 DEG C, more preferably be not less than 100 DEG C, it is more excellent Glass transition temperature all when there are multiple glass transition temperatures is selected to be not less than 40 DEG C, most preferably all glass transition temperatures are equal Not less than 100 DEG C, help to embody the characteristics such as the hardness under material at high temperature dimensional stability, shape memory, low temperature and room temperature, Materials or the products such as the readily available gel with property, foam, ordinary solid；Another preferred embodiment is group At least one glass transition temperature of point A is higher than 25 DEG C but is lower than 40 DEG C, help to obtain that size is relatively stable, dynamic is suitable In, the higher elastomer of temperature sensitivity, foam and ordinary solid etc.；Another preferred embodiment is poly- for the dynamic At least one glass transition temperature of polymer composition component A is not higher than 25 DEG C, and in addition at least one glass transition temperature Degree is not less than 100 DEG C, can take into account low temperature and high-temperature behavior.

In embodiments of the present invention, cross-linked network included in the component A at least one, either Single one network can also have the multiple networks being mutually blended, and can also have multiple networks of interpenetrating, can also exist simultaneously Blending and interpenetrating, etc.；It can be using any appropriate crosslinking topological structure, chemical structure, reactive mode and combinations thereof etc..

In embodiments of the present invention, containing at least one unsaturated triple carbon-carbon bonds in the component A, as dynamic The polymerization linking point or crosslinking linking point of state polymer exist as polymerization linking point and crosslinking linking point simultaneously.This Outside, the present invention is not excluded for group presence of the triple carbon-carbon bonds as side group, end group and other positions.In embodiments of the present invention In, the type of the triple carbon-carbon bonds is not particularly limited, there is the structure being shown below:

Wherein,Indicate the connection with polymer chain or any other suitable group/atom (including hydrogen atom).

In the present invention, unless making the triple carbon-carbon bonds that irreproducibility dissociation occur using specific method, otherwise Degradability variation will not occur for covalent cross-linking network and covalent polymer chain.It is preferred that triple carbon-carbon bonds exist only in the chain of cross-linked network On skeleton.

In embodiments of the present invention, also selectively containing the hydrogen bond that can form supermolecule hydrogen bond action in component A Group.When including simultaneously supermolecule hydrogen bond action in component A, network structure is more rich and varied, and energy absorption performance is more preferably.When In component A simultaneously include supermolecule hydrogen bond action when and included cross-linked network quantity be it is two or more when, these networks It can be identical or different；It only includes what supermolecule was crosslinked that can be subnetwork only, which include dynamic covalent cross-linking and subnetwork, Combination, or part only include dynamic covalent cross-linking and part while including the group that dynamic covalent cross-linking and supermolecule are crosslinked It closes, or the combination that part is only crosslinked comprising dynamic covalent cross-linking and supermolecule comprising supermolecule crosslinking and part simultaneously, or Person be in each network all while including dynamic covalent cross-linking and supermolecule crosslinking, but the present invention is not limited only to this.

(the first network structure) in a preferred embodiment of the present invention, only one friendship in the component A It networks network, dynamic covalent cross-linking is only contained in the cross-linked network, the degree of cross linking reaches its gel point or more.The network structure structure Simply, dynamic covalent cross-linking can keep balanced structure, and provide covalent dynamic under given conditions.

In another preferred embodiment of the present invention (second of network structure), only one in the component A Cross-linked network is crosslinked containing dynamic covalent cross-linking and supermolecule in the cross-linked network, wherein the crosslinking of dynamic covalent cross-linking simultaneously Degree reaches its gel point or more, and the degree of cross linking of supermolecule crosslinking is in its gel point above and below.In the network structure, by dynamic State covalent cross-linking can keep balanced structure, and supermolecule crosslinking provides dynamic；Under given conditions, dynamic covalent cross-linking It can provide covalent dynamic.

In another preferred embodiment of the invention (the third network structure), there was only one in the component A A cross-linked network is crosslinked containing dynamic covalent cross-linking and supermolecule in the cross-linked network, wherein the friendship of dynamic covalent cross-linking simultaneously Connection degree is in its gel point hereinafter, the degree of cross linking of supermolecule crosslinking is more than its gel point.The network structure has good dynamic Property, it is based particularly on the strain-responsive of supermolecule crosslinking；Dynamic covalent cross-linking does not keep balanced structure directly, but specific Under conditions of, dynamic covalent cross-linking also can provide additional covalent dynamic and play the role of regulation performance.

In another preferred embodiment of the invention (the 4th kind of network structure), there was only one in the component A A cross-linked network is crosslinked containing dynamic covalent cross-linking and supermolecule in the cross-linked network, wherein the friendship of dynamic covalent cross-linking simultaneously Connection degree in its gel point hereinafter, supermolecule crosslinking the degree of cross linking in its gel point hereinafter, but the sum of the two degree of cross linking in gel point More than.Dynamic covalent cross-linking and the degree of cross linking of supermolecule crosslinking are lower in the network structure, the whole degree of cross linking of network structure Not high, dynamic covalent cross-linking and supermolecule crosslinking are most important to the effect for providing balanced structure regulation performance.

In another preferred embodiment of the present invention (the 5th kind of network structure), contain in the component A there are two Network；Dynamic covalent cross-linking is contained only in 1st network, the degree of cross linking is more than its gel point；Supermolecule friendship is contained only in 2nd network Connection, the degree of cross linking is more than its gel point.In the network structure, the 2nd network has good dynamic, and the 1st network provides flat Weigh structure, by the interpenetrating of two networks or the combinations such as Semi-IPN, can preferably play comprehensive effectiveness；In specific item Under part, dynamic covalent cross-linking also can provide additional covalent dynamic and play the role of regulation performance.

In another preferred embodiment of the present invention (the 6th kind of network structure), contain in the component A there are two Network；Covalent cross-linking containing dynamic and supermolecule are crosslinked in 1st network, are contained dynamic covalent cross-linking in the cross-linked network simultaneously and are surpassed Molecule cross-link, wherein the degree of cross linking of dynamic covalent cross-linking is more than its gel point, and the degree of cross linking of supermolecule crosslinking is in its gel point Above and below；Supermolecule covalent cross-linking is contained only in 2nd network, the degree of cross linking is more than its gel point.In the network structure, lead to The combinations such as the interpenetrating of two networks are crossed, comprehensive effectiveness can be preferably played；And it can be using super in two networks Molecule cross-link provides collaboration or orthogonal dynamic.

In another preferred embodiment of the present invention (the 7th kind of network structure), one is contained in the component A Network, wherein only containing dynamic covalent cross-linking more than gel point, the supermolecule degree of cross linking is poly- in its gel point supermolecule below Object is closed to be dispersed in dynamic covalent cross-linking network.In the network structure, dynamic covalent cross-linking can keep balanced structure, specific Under conditions of, dynamic covalent cross-linking also can provide covalent dynamic；Supermolecule polymer dispersed therein provides dynamic, special It is not strain-responsive.

In another preferred embodiment of the present invention (the 8th kind of network structure), one is contained in the component A Network is crosslinked containing dynamic covalent cross-linking and supermolecule in the cross-linked network, wherein the degree of cross linking of dynamic covalent cross-linking reaches simultaneously To more than its gel point, the degree of cross linking of supermolecule crosslinking is in its gel point above and below；The supermolecule degree of cross linking is in its gel point Supermolecule polymer below is dispersed in dynamic covalent cross-linking network.In the network structure, dynamic covalent cross-linking can be kept Balanced structure, under given conditions, dynamic covalent cross-linking also can provide covalent dynamic；Supermolecule crosslinking provides dynamic, Supermolecule polymer dispersed therein provides supplement dynamic, especially strain-responsive.

In another preferred embodiment of the present invention (the 9th kind of network structure), one is contained in the component A Network, wherein only containing dynamic covalent cross-linking more than gel point, supermolecule of the supermolecule degree of cross linking more than its gel point is poly- Object is closed to be dispersed in dynamic covalent cross-linking network with graininess.In the network structure, dynamic covalent cross-linking can keep balancing Structure, under given conditions, dynamic covalent cross-linking also can provide covalent dynamic；Supermolecule polymer particle provide filling and Dynamic can obtain local viscosity and intensity in strain-responsive and increase.

In another preferred embodiment of the present invention (the tenth kind of network structure), one is contained in the component A Network is crosslinked containing dynamic covalent cross-linking and supermolecule in the cross-linked network, wherein the degree of cross linking of dynamic covalent cross-linking reaches simultaneously To more than its gel point, the degree of cross linking of supermolecule crosslinking is in its gel point above and below；The supermolecule degree of cross linking is in its gel point Above supermolecule polymer is dispersed in dynamic covalent cross-linking network with graininess.In the network structure, dynamic is covalently handed over Connection can keep balanced structure, and under given conditions, dynamic covalent cross-linking also can provide covalent dynamic；Supermolecule crosslinking mentions For dynamic, supermolecule polymer particle provides filling and supplement dynamic, and local glue can be obtained in strain-responsive Degree and intensity increase.

In the present invention, by dynamic covalent cross-linking in conjunction with supermolecule cross-linked phase, there can also be other diversified realities Apply mode.Those skilled in the art can rationally and effectively be realized with logic according to the present invention and train of thought.

In the present invention, the hydrogen bond group for forming supermolecule hydrogen bond action includes being present in polymer chain skeleton Go up the hydrogen bond group (calling " skeleton hydrogen bond group " in the following text) of (including on main chain/side chain/branch/bifurcated chain backbone) and in polymerization The hydrogen bond base of hydrogen bond group (calling " side group hydrogen bond group " in the following text) and polymer chain and other compound ends in object chain side group Group's (calling " end group hydrogen bond group " in the following text).The skeleton hydrogen bond group refers to that at least one atom in the group directly participates in The building polymer chain skeleton, including main polymer chain, side chain, branch, bifurcated chain skeleton；The side group hydrogen bond base Group, refers to all atoms on the group in side group；The end group hydrogen bond group refers to all atoms on the group On end group.

In embodiments of the present invention, the hydrogen bond group can be with skeleton hydrogen bond group, side group hydrogen bond group, end The combination of any one or more of the forms such as base hydrogen bond group is present in the dynamic aggregation compositions.Due to part Hydrogen bond, which does not have directionality and selectivity, can form hydrogen bond action under specific circumstances between the hydrogen bond group of different location, Hydrogen bond can be formed between each other between the hydrogen bond group of identical or different position in identical or different polymer molecule Effect, can also be with hydrogen of the other compositions in polymer as contained by optional other polymers molecule, filler, small molecule etc. Hydrogen bond action is formed between key group.As an example, the present invention in hydrogen bond action include but is not limited to such as: the side chain and/ Or the hydrogen bond group in side group forms interchain hydrogen bond crosslinking between different molecular；Hydrogen bond group in the side chain and/or side group It is crosslinked with interchain hydrogen bond is formed in the main chain backbone between hydrogen bond group；Hydrogen bond base in the part side chain and/or side group Chain inner ring is independently formed with hydrogen bond between group；Chain is independently formed with hydrogen bond between hydrogen bond group in the main chain backbone of part Inner ring；Hydrogen bond group collective effect in the part side chain and/or side group forms chain inner ring etc. with hydrogen bond.It may be noted that It is to be not excluded for part in the present invention and be formed by intrachain hydrogen bond effect and neither formed inter-chain action nor to form chain inner ring, only shape The effects of at grafting is included but are not limited to.

In embodiments of the present invention, the position of hydrogen bond group does not have any restriction, can be any appropriate position. In the preferred embodiment of the present invention, pendant hydrogen key group is only contained in the component A；It is excellent in another kind of the invention It selects in embodiment, main chain backbone hydrogen bond group is only contained in the component A；In another preferred embodiment of the invention In, side chain skeleton hydrogen bond group is only contained in the component A；In another preferred embodiment of the invention, the component A In only contain side chain end group hydrogen bond group；In another preferred embodiment of the invention, only contain main chain in the component A End group hydrogen bond group；In another preferred embodiment of the invention, pendant hydrogen key group and side are only contained in the component A Chain backbone hydrogen bond group；In another preferred embodiment of the invention, in the component A only containing pendant hydrogen key group and Main chain backbone hydrogen bond group；In another preferred embodiment of the invention, pendant hydrogen key group is only contained in the component A With main chain end group hydrogen bond group；In another preferred embodiment of the invention, pendant hydrogen key base is only contained in the component A Group and side chain end group hydrogen bond group；In another preferred embodiment of the invention, side chain end group is only contained in the component A Hydrogen bond group and main chain backbone hydrogen bond group；In another preferred embodiment of the invention, only contain side in the component A Chain end group hydrogen bond group and main chain end group hydrogen bond group；In another preferred embodiment of the invention, in the component A only Contain main chain end group hydrogen bond group and main chain backbone hydrogen bond group；In another preferred embodiment of the invention, described group Divide and only contains pendant hydrogen key group, side chain end group hydrogen bond group and main chain backbone hydrogen bond group in A；It is excellent in another kind of the invention It selects in embodiment, pendant hydrogen key group, side chain end group hydrogen bond group and main chain end group hydrogen bond base is only contained in the component A Group；In another preferred embodiment of the invention, pendant hydrogen key group, side chain end group hydrogen bond are only contained in the component A Group and side chain skeleton hydrogen bond group；In another preferred embodiment of the invention, only contain pendant hydrogen in the component A Key group, side chain skeleton hydrogen bond group and main chain end group hydrogen bond group；It is described in another preferred embodiment of the invention Only contain pendant hydrogen key group, side chain skeleton hydrogen bond group, side chain end group hydrogen bond group and main chain backbone hydrogen bond base in component A Group；In another preferred embodiment of the invention, pendant hydrogen key group, side chain skeleton hydrogen bond are only contained in the component A Group, side chain end group hydrogen bond group and main chain end group hydrogen bond group；In another preferred embodiment of the invention, described group Divide and contains side group hydrogen bond group, side chain end group hydrogen bond group, side chain skeleton hydrogen bond group, main chain end group hydrogen bond group and master in A Chain backbone hydrogen bond group.But the present invention is not limited only to this.

Since the general quantity of main chain backbone hydrogen bond group is than relatively limited and not easy to control, and the side chain/side group hydrogen bond base Group can before polymerized/cross-linked, later or in the process generate, before or after the quantity that generates can be than relatively freely controlling System, and side chain/side group hydrogen bond freedom degree is higher is more prone to produce dynamic, it is therefore preferable that side chain/side group hydrogen bond group, More preferable side group and side chain end group hydrogen bond group, most preferably side group hydrogen bond group.Side chain/between side group hydrogen bond group and chain backbone Link structure, length and the structure of itself include that substituent group and side group etc. can carry out diversified adjusting, to control HYDROGEN BOND INTENSITY, steric hindrance, thermal stability, glass transition temperature etc., and then regulate and control its dynamic property, it is different to assign polymer The performances such as ultra-tough, selfreparing, strain-responsive, shape memory.When hydrogen bond group be located at side group side chain, especially When the side group of the side chain with multilevel structure, is conducive to the density for adjusting hydrogen bond group, facilitates the control degree of cross linking and cross-linked structure And the performances such as dynamic and super toughness.

In embodiments of the present invention, the supermolecule hydrogen bond action by hydrogen bond group donor (H, that is, hydrogen Atom) and receptor (Y, that is, receive the electronegative atom of hydrogen atom) interaction formed, can be optional tooth number.Its In, the number of teeth refers to being formed by hydrogen bond quantity by the donor and receptor of hydrogen bond group, and each H ... Y group is combined into a tooth. In following formula, the bonding situation of the schematically illustrate tooth of difference, two teeth and three tooth hydrogen bonds.

The bonding situation of one tooth, two teeth and three tooth hydrogen bonds can concrete example it is as follows:

In embodiments of the present invention, the number of teeth of hydrogen bond is not limited.The number of teeth of hydrogen bond is more, and synergistic effect is got over Greatly, the intensity of hydrogen bond is bigger.If the number of teeth for being formed by hydrogen bond is more, intensity is big, then the dynamic of hydrogen bond action is just It is weak, it can be used as structural hydrogen bond and play promotion dynamic aggregation object holding balanced structure and improve mechanical property (modulus and intensity) Effect.If the number of teeth of formed hydrogen bond is few, intensity is low, and the dynamic of hydrogen bond action is with regard to strong.It is a kind of preferred in the present invention Embodiment for select be no more than four teeth hydrogen bond dynamic is provided；Another preferred embodiment is to select two kinds or two Kind or more hydrogen bond group form the different hydrogen bond of dynamic, multi-level dynamic is provided.

In embodiments of the present invention, the hydrogen bond action can be by existing between any appropriate hydrogen bond group Noncovalent interaction generates, and the hydrogen bond group can only contain hydrogen bond donor, or only contain hydrogen bond receptor, or contain simultaneously There are a hydrogen bond donor and receptor, preferably the hydrogen bond group simultaneously containing hydrogen bond donor and receptor is so that it can be separately formed hydrogen bond Effect, wherein the hydrogen bond group for containing hydrogen bond donor and receptor while described preferably comprises at least one secondary amino group.

Wherein, when containing the hydrogen bond group of hydrogen bond donor and receptor when described while and being located at side group and/or end group, more Preferably comprise at least one of following constituent:

Wherein,Indicate the connection with polymer chain, G is end group；It can be cyclic or not cyclic with G.

Wherein, X is each independently selected from oxygen atom or sulphur atom.

The structure of G is not particularly limited, respectively it is independent include but is not limited to linear chain structure, the branched structure containing side group or Cyclic structure.Wherein, cyclic structure is not particularly limited, and can be selected from aliphatic ring, aromatic ring, saccharide ring, condensed ring, preferably rouge Fat race ring.The structure of G is respectively independently preferably linear chain structure.

G can contain hetero atom, can also be free of hetero atom.

The carbon atom number of G is not particularly limited, and respectively independent is preferably 1~20, and respective independent more preferably 1~10.

G is each independently selected from hydrogen atom, halogen atom, C_1-20Alkyl, C_1-20Miscellaneous alkyl, substituted C_1-20Alkyl or substitution Miscellaneous alkyl.Wherein, the substitution atom in G or substituent group are not particularly limited, and are each independently selected from halogen atom, alkyl replaces Base contains heteroatomic substituent group.

G is respectively independently more preferably hydrogen atom, halogen atom, C_1-20Alkyl, C_1-20Unsaturated aliphatic hydrocarbyl moiety, aryl, aromatic hydrocarbons Base, C_1-20Miscellaneous alkyl, C_1-20Alkyl oxygroup acyl group, C_1-20Alkylthio acyl group and its any substituted form.

G is respectively independently more preferably hydrogen atom, halogen atom, C_1-20Alkyl, C_1-20Alkenyl, aryl, aryl, C_1-20Rouge Miscellaneous alkyl, heteroaryl, heteroaryl alkyl, C_1-20Alkoxyacyl, aryloxy acyl group, C_1-20Alkyl sulfenyl acyl group, artyl sulfo acyl Base and its any substituted form.

G is respectively independently more preferably hydrogen atom, halogen atom, C_1-20Alkyl, C_1-20Alkenyl, aryl, aryl, C_1-20Rouge Miscellaneous alkyl, heteroaryl, heteroaryl alkyl, C_1-20Alkoxy carbonyl, aryloxycarbonyl, C_1-20Alkyl sulfenyl carbonyl, artyl sulfo carbonyl Base, C_1-20Alkoxy carbonyl, aryloxy thiocarbonyl, C_1-20Alkyl sulfenyl thiocarbonyl, artyl sulfo thiocarbonyl and Its any substituted form.

Specifically, G is each independently selected from including but not limited to hydrogen atom, fluorine atom, chlorine atom, bromine atom, iodine atom, first Base, ethyl, n-propyl, isopropyl, butyl, amyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, ten Trialkyl, myristyl, pentadecyl, cetyl, heptadecyl, octadecyl, nonadecyl, eicosyl, allyl, Acrylic, vinyl, phenyl, aminomethyl phenyl, butyl phenyl, benzyl, methoxycarbonyl, ethoxy carbonyl, phenyloxycarbonyl, benzyl Epoxide carbonyl, methyl mercapto carbonyl, ethylmercapto group carbonyl, thiophenyl carbonyl, benzylthio carbonyl, B aminocarbonyl, benzylaminocarbonyl, first Oxygroup thiocarbonyl, ethyoxyl thiocarbonyl, phenoxythiocarbonyl, benzyloxy thiocarbonyl, methyl mercapto thiocarbonyl, second sulphur Base thiocarbonyl, phenylthiothiocarbonyl carbonyl, benzylthio thiocarbonyl, substituted C_1-20Alkyl, substituted C_1-20Alkenyl, replace Aryl, substituted aryl, substituted C_1-20Rouge miscellaneous alkyl, substituted heteroaryl, substituted heteroaryl alkyl, substituted C_1-20Alkane Epoxide carbonyl, substituted aryloxycarbonyl, substituted C_1-20Alkyl sulfenyl carbonyl, substituted artyl sulfo carbonyl, replace C_1-20Alkoxy carbonyl, substituted aryloxy thiocarbonyl, substituted C_1-20Alkyl sulfenyl thiocarbonyl, substituted virtue Base alkylthio carbonyl.Wherein, butyl includes but is not limited to normal-butyl, tert-butyl.Octyl includes but is not limited to n-octyl, 2- second Base hexyl.Wherein, atom or substituent group is replaced to be selected from halogen atom, hydrocarbyl substituent, contain heteroatomic substituent group.

It is preferably hydrogen atom, methyl, ethyl, n-propyl, isopropyl, normal-butyl, tert-butyl, penta that G is further respectively independent Base, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, myristyl, pentadecyl, 16 Alkyl, heptadecyl, octadecyl, nonadecyl, eicosyl, allyl, benzyl, trityl, phenyl, benzyl, methyl Benzyl, nitrobenzyl, tert. butyl-sulphenyl, benzyl sulfenyl, 2- pyridinylthio, acetyl group, benzoyl, 2- pyridylcarbonyl, Methoxycarbonyl, ethoxy carbonyl, t-butyloxycarbonyl, phenyloxycarbonyl, benzyloxycarbonyl, methyl mercapto carbonyl, ethylmercapto group Carbonyl, tert. butyl-sulphenyl carbonyl, thiophenyl carbonyl, benzylthio carbonyl, ethylenebis dithiocarbamate carbonyl, phenyl first thiocarbonyl, methoxyl group Thiocarbonyl, ethyoxyl thiocarbonyl, tert-butyl oxygroup thiocarbonyl, phenoxythiocarbonyl, benzyloxy thiocarbonyl, first sulphur Base thiocarbonyl, ethylmercapto group thiocarbonyl, tert. butyl-sulphenyl thiocarbonyl, phenylthiothiocarbonyl carbonyl, benzylthio thiocarbonyl, C_1-10It halohydrocarbyl, trifluoroacetyl group, halogenophenyl, halogeno-benzyl, nitrobenzophenone, nitrobenzyl and its any is substituted Form.Wherein, replace atom or substituent group is preferably fluorine atom, alkoxy, nitro.

G respectively independent more preferably hydrogen atom, methyl, ethyl, n-propyl, isopropyl, normal-butyl, tert-butyl, benzyl, triphen Methyl, phenyl, benzyl, methylbenzyl, tert. butyl-sulphenyl, benzyl sulfenyl, 2- pyridinylthio, 2- pyridylcarbonyl, tert-butyl Epoxide carbonyl, phenyloxycarbonyl, benzyloxycarbonyl, tert-butyl oxygroup thiocarbonyl, phenoxythiocarbonyl, the thio carbonyl of benzyloxy Base, tert. butyl-sulphenyl thiocarbonyl, phenylthiothiocarbonyl carbonyl, benzylthio thiocarbonyl, trifluoroacetyl group.

G is respectively independently more preferably hydrogen atom, methyl, ethyl, n-propyl, isopropyl, normal-butyl, tert-butyl, benzyl, three Benzyl, phenyl, benzyl, methylbenzyl, tert. butyl-sulphenyl, benzyl sulfenyl, 2- pyridinylthio.

G is respectively independently most preferably hydrogen atom, methyl, ethyl, n-propyl, normal-butyl.

Wherein, when containing the hydrogen bond group of hydrogen bond donor and receptor when described while and being located at main chain and/or side chain skeleton, At least one of its further preferably following constituent:

Wherein,Indicate the connection with polymer chain.

In another preferred embodiment of the invention, hydrogen bond group preferably is selected from carbamate groups, urea groups, thio Carbamate groups and the derivative of the above group etc., because of its abundant raw material, synthesis is simple, is suitble to industrialized production.

As an example, the hydrogen bond group in following side group and/or end group can be enumerated, but the present invention is not limited only to this.

Wherein, m, n, x are the quantity of recurring group, can be fixed value, are also possible to average value.M, n value range is 0 With the integer for being more than or equal to 1；X value range is the integer more than or equal to 1.

As an example, the hydrogen bond group on main chain and/or side chain skeleton as described below can be enumerated, but the present invention not only limits In this.

In embodiments of the present invention, the hydrogen bond group of hydrogen bond action is formed either mutual between different hydrogen bond groups Apotype combination is also possible to combining between hydrogen bond group of the same race from complementary type, makees as long as being capable of forming suitable hydrogen bond between group With.The combination of some hydrogen bond groups can be exemplified below, but the present invention is not limited only to this:

In the present invention, the supermolecule hydrogen bond action, which can be, carries out dynamic supermolecule crosslinking/poly- in dynamic aggregation object It is generated during conjunction；Dynamic supermolecule crosslinking/polymerization is carried out again after being also possible to pre-generated supermolecule hydrogen bond action；It can also After dynamic supermolecule crosslinking/polymerization is formed, to generate supermolecule hydrogen bond action during dynamic aggregation object subsequent forming, but The present invention is not limited only to this.

In embodiments of the present invention, except through forming hydrogen between hydrogen bond group present in the dynamic aggregation object Key effect is outer, can also form hydrogen bond by the hydrogen bond group and the hydrogen bond group in the other components introduced as additive Effect.Such other components that can participate in being formed hydrogen bond action include but is not limited to small molecule, inorganic material, metal material, Hydrogen bond group contained therein can be the group that hydrogen bond can be arbitrarily formed with the hydrogen bond group.Between such other components Hydrogen bond can also be formed.In the present invention, the content of other such hydrogen bond groups is not particularly limited, preferably shorter than hydrogen bond group The 50mol% of total content, more preferably less than 20mol%, even more preferably below 5mol%.

The triple carbon-carbon bonds group that reversible dynamic crosslinking is used to form in the present invention, which can be, has contained carbon carbon from selection The polymer precursor of three keys can also introduce on the basis of being free of the polymer precursor of triple carbon-carbon bonds.The introducing of triple carbon-carbon bonds, It can be carried out before covalent cross-linking or in the process.

Wherein, containing the polymer precursor of triple carbon-carbon bonds, as an example, including but not limited to polyhenylene ethynylene and its The poly- silicon-carbon alkane etc. of copolymer, polydiacetylene and its copolymer, main chain containing alkynyl.

Wherein, the group containing triple carbon-carbon bonds or introducing for segment can use any appropriate reaction, including but not only Be limited to Types Below: isocyanates and amino, hydroxyl, sulfydryl, carboxyl, epoxy group are reacted, carboxylic acid, carboxylic acid halides, acid anhydrides, active ester It is reacted with amino, hydroxyl, sulfydryl, free radical acrylate reaction, acrylamide radical reaction, double bond radical reaction, Epoxy group and amino, hydroxyl, sulfydryl react, phenol-formaldehyde reaction, nitrine-alkynes click-reaction, tetrazine-norbornene reaction, silicon hydroxyl Base condensation reaction；Preferred isocyanate and amino, hydroxyl, sulfydryl react, carboxylic acid halides, acid anhydrides and amino, hydroxyl, sulfydryl it is anti- It answers, free radical acrylate reaction, acrylamide radical reaction, double bond radical reaction, epoxy and amino, hydroxyl, sulfydryl Reaction.As an example, the available small organic agents containing triple carbon-carbon bonds include but is not limited to following lifted: butine two Alcohol, diethoxy butynediols, 2,4- hexadiine -1,6- glycol, 3,5- diine -1,8- ethohexadiol, acetylenedicarboxylic acid, 10,12- bis- Bis- (3- aminobenzene) diacetylene of 12 carbon diine diacid, 1,4-, 4- (3- aminophenyl) -2- methyl -3- butyne-2-alcohol, 4- hydroxyl Butyl- 2- acetylenic acid, bis- (trichlorine silicon substrate) acetylene etc., can also select on the chain backbone of end group functional containing the oligomeric of triple carbon-carbon bonds Object.

Wherein, the generation of triple carbon-carbon bonds can use any appropriate method, include but are not limited to following lifted: two Halide and vinyl halides dehydrohalogenation, tetrahalide dehalogenate, vinethene dealcoholysis, the elimination of β-cloroecther, α-diketone and alkene The deoxidation of glycol, the indirect dehydration of ketone, the thermal decomposition of acyl group ylide, the hydrocarbonylation of alkynes metal, alkynyl salt compounded of iodine and nucleopilic reagent Hydrocarbonylation, the oxidative coupling of alkynes, alkynes and the coupling of halogenated alkynes, the rearrangement of diazene, α, α-dichloro sulfone dehydrohalogenation weight Row, α, the dehydrohalogenation rearrangement of α-two bromoketone, diine metathesis reaction, cycloalkyne ring-opening reaction etc..

The generation or introducing of the hydrogen bond group of supermolecular mechanism are used to form in the present invention, can dynamic covalent cross-linking it Before, carry out later or in the process.It is preferred that carrying out before dynamic covalent cross-linking or in the process, more preferably covalently handed in dynamic It is carried out before connection.Because must will be generally added by way of swelling in relation to reagent if being carried out after dynamic covalent cross-linking, Complex process and effect is poor.

In embodiments of the present invention, the generation or introducing of hydrogen bond group can use any appropriate reaction, including but Be not limited only to Types Below: isocyanates and amino, hydroxyl, sulfydryl, carboxyl react, free radical acrylate reaction, double bond Radical reaction, double bond cyclization, epoxy and amino, hydroxyl, sulfydryl react, nitrine-alkynes click-reaction, and sulfydryl-double bond/ Alkynes click-reaction, the reaction of urea-amine, amidation process, tetrazine-norbornene reaction, active ester and amino, hydroxyl, sulfydryl Reaction, silicone hydroxyl condensation reaction；Preferred isocyanate and amino, hydroxyl, sulfydryl react, the reaction of urea-amine, amidation Reaction, active ester and amino, hydroxyl, sulfydryl react.In any one network structure, hydrogen bond group can have one or its Above reaction type, reaction means and the structure.

In embodiments of the present invention, for connecting dynamic covalent bond and dynamic covalent bond, dynamic covalent bond and hydrogen bond The ingredient of group, hydrogen bond group and hydrogen bond group can be small molecule and/or polymer segment.The wherein polymer chain Section, including but are not limited to main chain is carbon-chain structure, carbon heterochain structure, carbon chain structure, element chain structure, element heterochain knot The polymer segment of the miscellaneous element chain structure of structure, carbon.The carbon-chain structure is the structure that main chain backbone contains only carbon atom；It is described Carbon heterochain structure be main chain backbone contain simultaneously carbon atom and it is any or appoint several heteroatomic structures, wherein the miscellaneous original Son includes but are not limited to sulphur, oxygen, nitrogen；The carbon chain structure be main chain backbone contain simultaneously carbon atom and it is any or Appoint the structure of several Elements Atoms, wherein Elements Atom includes but are not limited to silicon, boron, aluminium；Based on the element chain structure Chain backbone is only containing the structure of Elements Atom；The element heterochain structure is main chain backbone simultaneously and only containing at least one miscellaneous The structure of atom and at least one Elements Atom；The miscellaneous element chain structure of the carbon is main chain backbone while including carbon atom, miscellaneous The structure of atom and Elements Atom.In an embodiment of the invention, it is carbon that the preferably described polymer segment, which is main chain, The polymer segment of chain structure and carbon heterochain structure, because of its structure-rich, has excellent performance.As an example, preferred carbochain and carbon Heterochain polymer segment is included but are not limited to such as acrylic polymer, saturation of olefins quasi polymer, ethylenic unsaturation hydro carbons Polymer, polystyrenic polymer, halogen-containing olefin polymer, polyacrylonitrile quasi polymer, polyvinyl alcohol Type of Collective Object, poly- (2- oxazoline) quasi polymer, polyether-based polymers, polyester polymer, Biopolvester quasi polymer, polycarbonate are birdsed of the same feather flock together Close object, polyurethane polymer, polyureas quasi polymer, polyamide polymers, polyamine quasi polymer, liquid crystal quasi polymer, ring Homopolymer, copolymer, modifier, the derivative etc. of oxygen quasi polymer, polysulfide ether polymer etc..In another reality of the invention It applies in mode, preferably the polymer segment is element heterochain structure, by way of example, such as all kinds of poly-organosilicon polymer.Make For citing, preferred polymer segment includes but are not limited to acrylic polymer, saturation of olefins quasi polymer, unsaturation Olefin polymer, halogen-containing olefin polymer, poly- (2- oxazoline) quasi polymer, polyether-based polymers, polyester Type of Collective Object, Biopolvester quasi polymer, polyurethane polymer, polyureas quasi polymer, polysulfide ether polymer, silicone-based polymers Deng homopolymer, copolymer, modifier, derivative etc..Specifically, currently preferred polymer segment includes but are not limited to Polymethyl acrylate, polyethyl acrylate, butyl polyacrylate, polyethylene, polypropylene, polyisobutene, polybutadiene, polycyclic are pungent Alkene, polynorbornene, polyisoprene, polyvinyl chloride, poly- (2- oxazoline), polyethylene glycol, polypropylene glycol, polycaprolactone, poly- β- Homopolymer, copolymer, modifier, the derivative of butyric ester, polyurethane, polyureas, polythiaether, polyorganosiloxane etc. Deng.

In yet another embodiment of the present invention, it is preferably described for connect dynamic covalent bond and dynamic covalent bond, The glass transition temperature of the polymer segment of dynamic covalent bond and hydrogen bond group, hydrogen bond group and hydrogen bond group is not higher than 25 DEG C, more preferably no higher than 0 DEG C, it is presented as flexibility, the convenient processing for carrying out subsequent products at normal temperature at room temperature before the reaction Preparation facilitates and obtains flexible and viscosity product, is also convenient for by increasing crosslink density or adjusting material using other additives The hardness for expecting matrix is conducive to embody the dynamic of supermolecule hydrogen bond as matrix.In another embodiment of the invention In, preferably the glass transition temperature of the polymer segment is not less than 40 DEG C, more desirably not less than 100 DEG C, is conducive to draw Enter the characteristics such as shape memory, high temperature dimensional stability, low temperature and room temperature hardness.In yet another embodiment of the present invention, It is preferred that the glass transition temperature of the polymer segment is higher than 25 DEG C but is lower than 40 DEG C, be conducive to introduce temperature sensitivity, The characteristics such as moderate elasticity and dynamic.In yet another embodiment of the present invention, in the preferably described polymer segment extremely A kind of few polymer segment that 25 DEG C are not higher than for glass transition temperature, and at least one is not less than for glass transition temperature 100 DEG C of polymer segment, convenient for obtaining the various characteristics under low temperature and high temperature simultaneously.

In embodiments of the present invention, for connecting dynamic covalent bond and dynamic covalent bond, dynamic covalent bond and hydrogen bond Group, the small molecule of hydrogen bond group and hydrogen bond group and/or polymer segment and/or dynamic aggregation object can have any conjunction Suitable topological structure includes but are not limited to linear chain structure, branched structure (including but not limited to starlike, H-type, dendroid, comb It is shape, hyperbranched), cyclic structure (including but not limited to monocycle, polycyclic, bridged ring, grommet, torus), two-dimensional/three-dimensional cluster structure and Its two kinds or several combination；Wherein, the linear chain structure of synthesis and control structure, the branched structure of structure-rich are preferably facilitated With can be with the two-dimensional/three-dimensional cluster structure of local enhancement, more preferable linear chain structure and branched structure.In the present invention, or even not It excludes to carry out the reaction such as further polymerized/cross-linked and connection using the polymer beads of crosslinking.

Selected above-mentioned each quasi polymer and its segment in the present invention, i.e., have hydrogen bond base containing dynamic covalent bond simultaneously again The polymer and its segment of group, the polymer for not only not contained dynamic covalent bond but also not contained hydrogen bond group and its segment only contain Polymer and its segment and only polymerization containing hydrogen bond group without dynamic covalent bond of the dynamic covalent bond without hydrogen bond group Object and its segment can directly select the raw material of commercialization, can also voluntarily polymerize.Polymerization is according to selected polymer Type includes but is not limited to polycondensation, addition polymerization and ring-opening polymerisation；Wherein, addition polymerization includes but is not limited to free radical polymerization, activity freedom Base polymerization, anionic polymerisation, cationic polymerization, coordination polymerization etc..Wherein, polymerization process can carry out in a solvent, can also be with It is solvent-free bulk polymerization.Specifically, as an example, the available polymerization of the present invention includes but is not limited to: styrene Class, the heat of (methyl) acrylic ester monomer cause general radical polymerization, phenylethylene, (methyl) acrylic ester monomer Light lnduced Free Radicals polymerization, the Iniferter free radical polymerization of vinyl chloride monomer, phenylethylene, (methyl) acrylic acid The atom transfer radical polymerization (ATRP) of esters monomer, phenylethylene, (methyl) esters of acrylic acid, acrylonitrile monomer are reversible Addition-fracture transferring free-radical polymerization (RAFT), nitroxide-mediated stable free-radical polymerization (NMP), ethylene, propylene coordination polymerization, benzene second The anionic polymerisation of vinyl monomer, lactone ring opening polymerization, lactams ring-opening polymerisation, epoxy addition polymerization, binary acid and dihydric alcohol Between polycondensation, the polycondensation between binary acid and diamine, between binary mercaptan and binary alkene/alkynes click-reaction polymerization, two Click-reaction polymerization between first nitrine and binary alkynes, the ring-opening polymerisation of 2- oxazoline derivative, polyurethane/polyurea reaction etc..? In specific implementation process, raw materials of compound can utilize above-mentioned any polymerisation process, appoint by the way that this field is general A kind of suitable polymerization technique is implemented, to obtain dynamic aggregation object of the invention.

It can be addition-crosslinked or condensation cross-linking for the mechanism of crosslinking of polymer.Wherein, it is addition-crosslinked refer to pass through addition Form and the cross-linking polymerization carried out, usually by the addition reaction containing multi-functional strand by intermolecular functional group And cross-linking products are formed, it is generated without by-product.Condensation cross-linking refers to the cross-linking reaction carried out by condensed forms, usually By forming cross-linking products by intermolecular functional group's condensation reaction containing multi-functional strand, there is by-product generation.

In embodiments of the present invention, crosslinking can be using any appropriate physics and chemical crosslinking technique.Physics is handed over Connection technique includes but is not limited to heat initiation crosslinking, photo-initiated crosslinking, radiation-induced crosslinking, plasma causes crosslinking, microwave draws Hair crosslinking etc.；Chemical crosslinking technique includes but is not limited to peroxide crosslinking, nucleopilic reagent substitution crosslinking, isocyanates reaction friendship Connection, epoxy reaction crosslinking, acrylate reactions crosslinking etc..Cross-linking process can be carried out in the form of ontology, solution, lotion etc..When Using bulk form, solid end product is conveniently directly obtained；When using solution form, gel is conveniently directly obtained；When using cream Liquid mode facilitates and obtains particle dispersing but with tack.It should be pointed out that any crosslinking must assure that the carbon carbon Three keys complete is incompletely dissociated the disintegration that can lead to covalent cross-linking network.

Initiator needed for above-mentioned polymerization, cross-linking method and polymerization, cross-linking process, catalyst, crosslinking agent, other Auxiliary agent and reaction condition etc. are all open known routine techniques (such as Pan Zuren chief editor, " polymer chemistry (enhanced editions) "), Those skilled in that art, which can according to need, to be reasonably selected and combines.

It is illustrated below for the embodiment of the part preparation method of network structure of the invention.

For example, second of network structure of the invention can be prepared by following methods: side hydrogen bond group (following knots will be had R is denoted as in structure formula_H) double acid chloride group monomers and (V is denoted as in following structural formula containing triple carbon-carbon bonds group_m) double carboxylic monomers And polyhydroxy based cross-linker reacts jointly, and second of network structure in the present invention can be formed with polymerized/cross-linked.It is single by control The formula rate of body and crosslinking agent, the content and ratio of dynamic covalent bond and hydrogen bond group, make in network in adjustable network Covalent cross-linking reach covalent gel point or more.

For another example, the 4th kind of network structure of the invention can be realized by the ring-opening polymerisation of cycloalkyne: will have side group hydrogen bond base Group R_HWith triple carbon-carbon bonds group V in ring_mCycloalkyne and optionally only contain V_mCycloalkyne by the ring-opening polymerization of cycloalkyne, can To obtain the 4th kind of network structure in the present invention.Pass through control hydrogen bonds group and the recipe ratio for being free of hydrogen bond group monomer Example, the ratio of dynamic covalent bond and hydrogen bond group in adjustable network, make the supermolecule in network be crosslinked reach gel point with On.

For another example, second of network structure of the invention can also be by first carrying out non-cyclodiyne of the part containing hydrogen bond group Metathesis polymerization reaction, then be crosslinked and obtained.The formula of the non-cyclodiyne of hydrogen bond group is contained or not contain by controlling The dosage of ratio and crosslinking agent, the content and ratio of dynamic covalent bond and hydrogen bond group, make in network in adjustable network Covalent cross-linking reach covalent gel point or more.

The embodiment of other network structures in the present invention is similar, and those skilled in the art can be according to this hair Bright understanding selects suitable preparation means, reaches ideal purpose.

Heretofore described component A, except network structure can have and only one polymer network in addition to, other networks Structure can the Multi net voting structure based on two or its above network.In addition to common blending dispersion, more preferably by two Or more than two polymer networks are intertwined the interpenetrating networks for tangling and being formed.Interpenetrating net polymer structure is due to network component Between collaboration and/or orthogonal effect so that its performance is substantially better than single network polymer of its component, generate more higher than single network The mechanical properties such as toughness, in the case where being based particularly on mentality of designing introducing hydrogen bond crosslinks of the invention.

In the present invention, two classes can be classified as according to polymers compositions crosslinking situation in composition interpenetrating networks, it is Semi-IPN With full interpenetrating.Only a kind of component is covalent cross-linking in Semi-IPN, and another component is worn in the form of non-covalent strand It inserts and becomes entangled in covalent cross-linking component.Between ignore network if supermolecule crosslinking that may be present, of the invention the 7th kind Network structure and the 8th kind of network structure can be considered semi-intercrossing network, the 5th kind of network structure of the invention and the 6th kind of network Structure can be considered full interpenetrating networks.

Traditional interpenetrating net polymer preparation method generally includes one-step method interpenetrating and two-step method interpenetrating.One-step method i.e. one All the components are added secondary property, then carry out polymerized/cross-linked, prepare target network.Two-step method first prepares the 1st network polymerization And then object is immersed in the monomer/pre-polymer solution to form the 2nd network, then cause polymerized/cross-linked and obtain target network Network.The preparation of dynamic aggregation object in the present invention can also use one-step method interpenetrating and two-step method interpenetrating, under specific circumstances also Must using three steps and its more than method.

It is illustrated below for the embodiment of the part preparation method of interpenetrating net polymer of the invention.With It is lower to lift only as an example, it not limits the scope of the invention, is lifted the present invention is not limited to following.

For example, the dynamic aggregation object is made of two networks in the 5th kind of network structure of the invention.Firstly, Preparing one kind, there is no hydrogen bond groups, but in the presence of the insatiable hunger that alkynes cross metathesis metathesis reaction can occur on polymer chain skeleton With the polymer dynamic co-crosslinking network of triple carbon-carbon bonds group.Then, gained dynamic covalent networks are swollen, are crosslinked with supermolecule The monomer or prepolymer of network, crosslinking agent etc. are uniformly mixed, and carry out supermolecule crosslinking, so that full interpenetrating net polymer is obtained, Namely Supramolecular Network disperses through in dynamic covalent cross-linking.Alternatively, by the monomer of dynamic covalent cross-linking network or prepolymer, Crosslinking agent is uniformly mixed with the monomer of supermolecule cross-linked network or prepolymer, crosslinking agent etc., at the same carry out dynamic covalent cross-linking and Supermolecule is crosslinked to arrive the 5th kind of network structure of the invention.

For another example, in the 8th kind of network structure of the invention, firstly, reasonably selecting preceding method preparation simultaneously containing dynamic The cross-linked network with second of network structure of covalent cross-linking and supermolecule crosslinking.Then, by resulting cross-linked network and super Molecularly Imprinted Polymer is sufficiently blended to arrive semi-interpenetrating network polymer.Alternatively, by the cross-linked network with second of network structure Monomer or prepolymer, crosslinking agent be uniformly mixed with supermolecule polymer, Mobile state covalent cross-linking of going forward side by side is to get to of the invention 8th kind of network structure.

In the following, to dynamic aggregation compositions component B catalyst or its compound (hereinafter referred to as " component in the present invention B ") it is described in detail.

In embodiments of the present invention, the alkynes cross metathesis metathesis reaction is urged based on metals such as molybdenum, tungsten It is carried out under the catalysis of agent comprising but it is not limited only to such as document " Alkyne Metathesis Catalysts:Scope And Future ", Andre Mortreux, Olivier Coutelier, Journal of Molecular Catalysis A:Chemical, 2006,254,96-104, document " Practical New Silyloxy-Based Alkyne Metathesis Catalysts with Optimized Activity and Selectivity Profiles ", Johannes Heppekausen, Robert Stade, Richard Goddard, and Alois FurstnerGeorgios, J.Am.Chem.Soc.2010,132,11045-11057, book " Handbook of Metathesis " 2013Wiley-VCH Catalyst is suitable for the invention disclosed in Verlag GmbH, Weinheim., patent US6525197 etc..Selected Catalyst both can be used alone, and can also be used cooperatively with two or more；It can be directly dispersing in component A and use, It can also be used in the form of the compound containing catalyst, such as, but not limited to by either physically or chemically coating or loading It is used on organic and inorganic, polymer support, and (such as suitable temperature, pressure) has under the conditions of selfreparing with other There is the component of low-viscosity high-fluidity to be coated on together in microcapsules or microtubular to use；It can also be the nonactive of catalyst Form can be converted to active catalyst under the appropriate environmental stimuli such as such as heat, soda acid, illumination, free radical.Work as institute The catalyst of selection need to be with all kinds of group phases present in each analog assistant filler existing for component A and selectivity when being used alone Hold.Reasonably selecting catalyst carrier can be enhanced the dispersibility of catalyst or its compound in component A, reduce catalytic clusters Partial size, to improve catalytic efficiency, reduce catalyst amount and reduce cost.Reasonably selecting covering material can also avoid urging Agent inactivates in composition preparation process or in the course of work.

The example of the available catalyst of the present invention includes but is not limited to following lifted:

Wherein, Py₃ForPh is phenyl, and t-Bu is tert-butyl.

Wherein, a kind of catalyst preferably to functional group with compatibility of component B, as an example, including but not It is limited to catalyst 15-20 etc.；The another kind of component B is preferably higher and insensitive to the air catalyst of catalytic efficiency, as Citing, including but not limited to catalyst 1,18-20 etc..The another kind of component B can preferably be played in room temperature or room temperature range The catalyst of catalytic action, as an example, including but not limited to catalyst 11.

In embodiments of the present invention, the preparation method of the compound containing catalyst is not particularly limited, and is used Method commonly known in the art.

As an example, a kind of preferred embodiment that the compound containing catalyst is prepared in the present invention is by catalyst packet It overlays in organic carrier.Available organic carrier is not particularly limited, and may be selected from but not limited to paraffin, poly- second as an example Glycol etc., it is known disclosed technological means that catalyst, which is coated on the method in organic carrier, and the present invention selects common system Preparation Method.For example, preferred the preparation method comprises the following steps: by selected catalysis by one kind of organic carrier coated catalysts of paraffin Agent, paraffin and surfactant are sufficiently blended under paraffin molten condition, and blend is poured into the stirring of certain revolving speed and temperature Higher than in the paraffin non-solvent of paraffin melting point；Stirring to being blended after liquid reaches stable state, be rapidly cooled to paraffin melting point with Under；Stop stirring, filtering obtains the catalyst composites of paraffin cladding.

Another preferred embodiment that the compound containing catalyst is prepared in the present invention is by selected catalyst Through physical absorption or chemical reaction load in organic or inorganic carrier.Available carrier is not particularly limited, as Example may be selected from but not limited to polystyrene resin beads, magnetic nano-particle, silica gel particle, molecular sieve, other mesoporous materials Deng being known disclosed technological means by method of the catalyst load on inorganic carrier, the present invention selects common preparation side Method.

Another preferred embodiment that the compound containing catalyst is prepared in the present invention is by catalyst and other choosings Auxiliary agent existing for selecting property is coated on using polymer as in the microcapsules of shell.Wherein, as the polymer of microcapsules outer wall without spy Other limitation as an example but is not limited to following lifted: natural polymer such as Arabic gum, sodium alginate, agar etc., semi-synthetic Macromolecule such as cellulose derivative, synthesis macromolecule for example poly- hydrocarbon, polyethers, polyurethane, polyureas, poly(urea formaldehyde), polyamide, gather polyester Vinyl alcohol, polysiloxanes etc..It is known disclosed technology that catalyst, which is coated on by the method in the microcapsules of shell of polymer, Means, for example, S.H.Cho etc. is at " Polydimethylsiloxane-Based Self-Healing Materials " The method for preparing polyurethane microcapsule is disclosed in Adv.Mater.2006,18,997-1000；For another example, E.N.Brown etc. exists 《In situ poly(urea-formaldehyde)Microencapsulation of Dicyclopentadiene》 The method of preparation ureaformaldehyde microcapsules is disclosed in J.Microencapsulation 2003,20,719-730.The present invention selects logical Normal preparation method.

In the following, existing for hybrid mode, existence form, other alternatives to dynamic aggregation compositions in the present invention Ingredient etc. is described in detail.

It in embodiments of the present invention, can be poly- by dynamic with any appropriate material hybrid mode known in the art Polymer component A (or each material in component A) and component B (or each material in component B) are by being mixed with dynamic aggregation object Composition can be interval, semicontinuous or continuous processing form mixing；Similarly, interval, semicontinuous or company also may be selected Continuous process form forms dynamic aggregation compositions.It is mixed that the hybrid mode of use includes but are not limited to solution stirring Close, melting is stirred, mediates, mixing, mill, melting extrusion, ball milling etc., wherein it is preferred that solution is stirred, melts stirring Mixing and melting extrusion.Energy in material mixed process provides form and includes but are not limited to heating, illumination, radiation, micro- Wave, ultrasound.The molding mode of use includes but are not limited to extrusion molding, injection moulding, compression molding, tape casting, calendering Molding, cast molding.

In embodiments of the present invention, it is stirred using solution and melting is stirred, mainly in a manner of following two Carry out: (1) being directly stirred reaction mass in the reactor or heating melting after be stirred reaction, such mode is general Reaction mass be liquid or lower melting-point solid or reaction mass is more difficult find cosolvent in the case where use；(2) will Reaction mass is dissolved in respective solvent or is stirred mixing in common solvent in the reactor, and such mode is general It is used in the case where reaction mass is higher fusing point or solid of not definite melting point.Mixing temperature is not particularly limited, and leads to Often at 0-200 DEG C, preferably 25-120 DEG C, more preferable 25-80 DEG C, mixing time is not particularly limited, and is preferably controlled in 1 point Clock is 10-120 minutes more preferable to 12 hours.The product obtained after mixing is poured into suitable mold, suitable Under the conditions of temperature, preferably at 0-150 DEG C, under the conditions of more preferable 25-80 DEG C of temperature, place the regular hour, preferably 0-48 hours Polymer samples can be obtained, this can remove solvent as needed in the process.

Used solvent in above-mentioned preparation method, it has to be possible to while dissolve reaction mass respectively, and dissolve There is the solvent of two class compounds to allow for dissolving each other, reaction mass is not precipitated in the mixed solvent, and solvent used includes but not It is only limitted to mixed solvent that is following any or appointing several solvents: methanol, ethyl alcohol, acetonitrile, acetone, butanone, benzene, toluene, diformazan Benzene, chlorobenzene, ethyl acetate, ether, methyl tertiary butyl ether(MTBE), tetrahydrofuran (THF), chloroform, methylene chloride, 1,2- dichloroethanes, 1,1,2,2- tetrachloroethanes, dimethyl sulfoxide (DMSO), dimethylformamide (DMF), dimethyl acetamide, N- crassitude Ketone, isopropyl acetate, n-butyl acetate, trichloro ethylene, mesitylene, dioxanes, trishydroxymethylaminomethane (Tris) buffering Liquid, citrate buffer solution, acetic acid buffer solution, phosphate buffer solution, borate buffer solution etc.；Preferred alcohol, toluene, chloroform, Methylene chloride, 1,2- dichloroethanes, DMF, phosphate buffer solution.

In embodiments of the present invention, the specific preparation of dynamic aggregation compositions material is mixed with using melting extrusion A certain amount of reaction mass, is usually added in extruder and carries out extrusion blending reaction by method, and extrusion temperature is not special Limitation, usually 0-280 DEG C, preferably 25-150 DEG C, more preferable 50-100 DEG C.Reaction product can be cut into conjunction after direct tape casting Suitable size, either carries out sample preparation using injection molding machine or moulding press.Injection temperature is not particularly limited, usually 0-280 DEG C, excellent Select 25-150 DEG C, more preferable 50-100 DEG C；Molding temperature is not particularly limited, usually 0-280 DEG C, preferably 25-150 DEG C, more It is preferred that 50-100 DEG C, clamp time is not particularly limited, usually 0.5-60min, preferably 1-10min.Batten is placed in properly Mold in, at 25-150 DEG C, under the conditions of preferably 50-80 DEG C of temperature, place 0-24h, obtain final composition sample.

In embodiments of the present invention, in the dynamic aggregation compositions, the quality of component A accounts for component A, B matter The range of the ratio of the sum of amount is 60-99.99%, and the range that the quality of component B accounts for the ratio of component A, B quality sum is 0.01-40% can also contain other components in composition.

In the present invention, the form of the dynamic aggregation compositions can be ordinary solid, elastomer, gel, bubble Foam etc..Wherein, the dissolvable small-molecular-weight component content contained in ordinary solid and foamed material is generally not more than 10wt%, and The small-molecular-weight component content contained in gel is generally not less than 50wt%.Ordinary solid mechanical property is good, mechanics of elastic bodies Energy is moderate but has the unexistent flexibility of ordinary solid, and preparation method is also most easy, therefore more preferably.Foam is due to light And hardness and bendable folding endurance are adjustable, and purposes is wide；In addition foam itself has certain cushion performance, in the present invention may be used It is promoted with obtaining the collaboration of energy absorption performance, therefore also more preferably.In embodiments of the present invention, it is combined in dynamic aggregation object Sweller can be introduced in object, prepare dynamic aggregation compositions gel.Gel products flexibility and bendable folding endurance are all good, and It can have certain toughness by structure and formula adjustment, because the material of many other forms can be incorporated there are sweller Expect unexistent beneficial constituent, there is special energy-absorbing purposes.Wherein, the sweller can include but is not limited to Solvent, water, ionic liquid, oligomer, plasticizer.

A kind of dynamic aggregation object gel provided by the present invention, including organic solvent gel, ionic liquid gel, oligomer Swell gel, plasticizer swell gel, hydrogel.Wherein, preferred ion liquid gel and plasticizer swell gel.

A kind of preferred preparation method of dynamic aggregation compositions ionic liquid gel of the invention includes but are not limited to Following steps: each raw material for preparing dynamic aggregation compositions component A, B and other raw materials are added in ionic liquid, made The sum of prepared mass fraction of dynamic aggregation compositions component A, B is 0.5~70%, is carried out by the appropriate means A kind of dynamic aggregation compositions ion is made after reaction in polymerization, coupling, crosslinking or other kinds of chemical reaction Liquid gel.The preferred preparation method of another dynamic aggregation compositions ionic liquid gel of the invention includes but is not limited to Following steps: by described dynamic aggregation compositions component A, B and and other raw materials swell in ionic liquid or containing ion In the solvent of liquid, making the sum of mass fraction of dynamic aggregation compositions component A, B is 0.5~70%, is sufficiently swollen A kind of dynamic aggregation object ionic liquid gel is made in the solvent for removing extra ionic liquid afterwards and selectively using.It is elected When selecting ionic liquid and catalyst, positive and negative ion, which should be avoided, causes catalyst or its compound to decompose inactivation.

A kind of preferred preparation method of dynamic aggregation compositions oligomer swell gel of the invention includes but not only limits In following steps: each raw material for preparing dynamic aggregation compositions component A, B and other raw materials and oligomer being blended, institute is made The sum of mass fraction of dynamic aggregation compositions component A, B of preparation is 0.5~70%, is gathered by the appropriate means It closes, be coupled, a kind of dynamic aggregation compositions oligomer is made after reaction in crosslinking or other kinds of chemical reaction Swell gel.The preferred preparation method of another dynamic aggregation compositions oligomer swell gel of the invention includes but unlimited In following steps: dynamic aggregation compositions component A, B and other raw materials are swollen in the solvent containing oligomer In, making the sum of mass fraction of dynamic aggregation compositions component A, B is 0.5~70%, sufficiently removes solvent after swelling, i.e., A kind of dynamic aggregation compositions oligomer swell gel is made.

A kind of preferred preparation method of dynamic aggregation compositions plasticizer swell gel of the invention includes but not only limits In following following steps: each raw material for preparing dynamic aggregation compositions component A, B and other raw materials are added to plasticizer In, making the sum of prepared mass fraction of dynamic aggregation compositions component A, B is 0.5~70%, passes through the suitable hand A kind of dynamic aggregation object combination is made after reaction in Duan Jinhang polymerization, coupling, crosslinking or other kinds of chemical reaction Object plasticizer swell gel.The preferred preparation method packet of another dynamic aggregation compositions plasticizer swell gel of the invention It includes but is not limited to following steps: dynamic aggregation compositions component A, B and other raw materials are swollen in containing plasticising In the solvent of agent, making the sum of mass fraction of dynamic aggregation compositions component A, B is 0.5~70%, sufficiently after swelling Except solvent, that is, a kind of dynamic aggregation compositions plasticizer swell gel is made.

A kind of preferred preparation method of dynamic aggregation compositions hydrogel of the invention includes but are not limited to as follows such as Lower step: each raw material for preparing dynamic aggregation compositions component A, B and other raw materials are added to the water, made prepared The sum of mass fraction of dynamic aggregation compositions component A, B is 0.5~70%, is polymerize by the appropriate means, is even It closes, a kind of dynamic aggregation object hydrogel is made after reaction in crosslinking or other kinds of chemical reaction.Of the invention is another A kind of preferred preparation method of dynamic aggregation compositions hydrogel includes but is not limited to following steps: by the dynamic aggregation Compositions component A, B and other raw materials are sufficiently swollen in water, make the quality of dynamic aggregation compositions component A, B The sum of score is 0.5~70%, removes extra water, that is, a kind of dynamic aggregation compositions hydrogel is made.Work as dynamic aggregation When object swells in water and forms hydrogel, catalyst that is insensitive to water and having enough solubility in water should be selected or its is compound Object.

In embodiments of the present invention, dynamic aggregation compositions can be prepared into foamed material.Wherein, foam includes soft Sex vesicle foam or semi-flexible, semi-rigid, micropore or rigid foam.

In embodiments of the present invention, the structure of dynamic aggregation compositions foamed material is related to open-celled structure, closed pore Three kinds of structure, half-open semi-closure structure etc..It in open-celled structure, is interconnected between abscess and abscess, or connection completely, one-dimensional or three Dimension can be transferred through gas or liquid, and abscess diameter is 0.01 to 3mm etc..Hole-closing structure has individual blisters structure, inner cell There is wall film to separate between abscess, the overwhelming majority is not interconnected, and abscess diameter is 0.01 to 3mm etc..Contained abscess It is existing to be interconnected again that have mutual disconnected structure be then half open-celled structure.

In embodiments of the present invention, foaming method is usual way, can be divided according to the difference of foaming agent used For physical blowing method and chemical blowing process two major classes.Foam can have water or it is anhydrous under the conditions of prepare, mechanical can send out Bubble or on-mechanical foaming.Further, the non-reacted foaming agent of auxiliary known in the art can be used in the preparation of foam.

A kind of preparation method of preferred dynamic aggregation compositions foam of the present invention includes the following steps: single in preparation When one network dynamic foam of polymers, two component reaction materials are first prepared.Reaction mass one includes all small points for generating component A The raw materials such as sub- monomer, chain extender, crosslinking agent and component B and the auxiliary agent needed for other；Reaction mass two includes foaming agent, bubble Foam stabilizers, the catalyst for being catalyzed foaming and/or polymerization crosslinking reaction and the auxiliary agent needed for other.Then by two components Reaction mass mixes according to a certain percentage, stirring, and carries out temperature control as needed, and the single network dynamic to be foamed is poly- Polymer composition.By the dynamic aggregation object that this preparation method prepares dynamic aggregation compositions foam be preferably based on polyurethane, The polymer of polyureas.

The preparation method of another preferred dynamic aggregation compositions foam of the invention is freeze-drying, including as follows Step: the dynamic aggregation compositions for swelling in volatile solvent are freezed, then close under vacuum condition with distillation Mode escapes solvent.During solvent evolution and after evolution, dynamic aggregation compositions can remain outer before freezing Thus shape obtains the foamed material of porous spongy.

In dynamic aggregation compositions foam preparation processes of the invention, when containing multiple polymer networks in foam, Multiple networks can generate simultaneously, can also be separately generated.

Dynamic aggregation compositions foamed material provided by the present invention further relates to: by welding, gluing, cutting, matching plane, Perforation, coining, lamination and hot forming, by the dynamic aggregation compositions foamed material be transformed into it is any need shape, Such as pipe, stick, sheath, container, ball, piece, volume and band；It, will be described dynamic by lamination, bonding, fusion and other interconnection techniques Known to state polymer composition foamed material and sheet material, film, foam, fabric, stiffener and those skilled in the art Other materials are combined into complicated interlayer structure together；The dynamic aggregation compositions foamed material is in washer or sealing Purposes；The purposes of the dynamic aggregation compositions foamed material in packaging material or in a reservoir.It is moved about of the invention State polymer composition, foamable dynamic aggregation compositions are such a types, allow to by extrusion, injection molding, Other forming techniques known to compression moulding or those of skill in the art deform them.

Foamed material provided by the present invention is different from common foamed material, three-dimensional prepared by common foamed material Once being formed, structure cannot change structure again, repair difficulty, not can be recycled after damaged；And foamed material provided by the present invention, Although the polymer network of three-dimensional crosslinking structure, can also be repaired after being ruptured under certain condition, or by moulding again Type or reclaiming are done him and are used, and there are hydrogen bond actions and dynamic covalent bond while reason is in network structure.The present invention Provided foamed material solves the problems, such as plastotype again, controllable reparation and the reclaiming of regular-type foam material.

Dynamic aggregation compositions material of the invention during the preparation process, in the range of not interfering the object of the invention, It can also according to circumstances select to be added or used to other polymers, auxiliary agent, filler, sweller to come collectively as dynamic aggregation object group The recipe ingredient for closing object, can improve material processing performance, improve product quality and yield, and reduce product cost or imparting Certain distinctive application performance of product, but these additives or using object it is not necessary to.

Wherein, the other polymers can play in system as additive and improve material property, assign material Material new capability improves materials'use and economic benefit, has the function that material comprehensively utilizes.Addible other polymers, It can be selected from natural polymer, synthetic macromolecular compound.The present invention is to the character of added polymer and is had Some molecular weight can be oligomer or high polymer according to the difference of molecular weight without limitation, according to the difference of polymeric species, Can be homopolymer or copolymer, in the specific use process should be according to the performance of target material and the need of actual fabrication process It wants and is selected.

When the other polymers are selected from natural polymer, it can be selected from following any or appoint several days Right high-molecular compound: natural rubber, chitosan, chitin, native protein, polysaccharide etc..

When the other polymers are selected from synthetic macromolecular compound, it can be selected from following any or appoint several: Polytrifluorochloroethylene, haloflex, chliorinated polyvinyl chloride, polyvinyl chloride, Vingon, low density polyethylene (LDPE), middle density Polyethylene, high density polyethylene (HDPE), ultra-high molecular weight polyethylene, melamine formaldehyde resin, polyamide, polyacrylic acid, polypropylene Acid esters, polyacrylamide, polyacrylonitrile, polybenzimidazoles, polyethylene terephthalate, polybutylene terephthalate Ester, polycarbonate, polyethylene glycol, polyester, polyether sulfone, polyarylsulfone (PAS), polyether-ether-ketone, tetrafluoroethylene-perfluoro propane copolymer, polyamides Imines, polyacrylate, polyacrylonitrile, polyphenylene oxide, polypropylene, polyphenylene sulfide, polyphenylsulfone, polystyrene, high-impact polyphenyl second Alkene, polysulfones, polytetrafluoroethylene (PTFE), polyurethane, polyureas, polyvinyl acetate, ethylene-propylene copolymer, ethane-acetic acid ethyenyl ester are total Polymers, AAS acrylonitrile acryloid styrene, acrylonitrile-butadiene-styrene copolymer, vinyl chloride-acetate Ester copolymer, polyvinylpyrrolidone, epoxy resin, phenolic resin, Lauxite, unsaturated polyester (UP), polyisoprene, gather it is suitable Butadiene, styrene-butadiene copolymer, hycar, poly- (the chloro- 1,3- butadiene of 2-), isobutene-are different Pentadiene copolymer, ethylene-propylene-Isosorbide-5-Nitrae-hexadiene copolymer, ethylene-propylene-dicyclopentadiene copolymer, ethylene-propylene- Ethylidene norbornene copolymer, dimethyl silicone polymer, Polymethyl methacrylate, polymethylphenylsiloxane, poly- methyl Vinyl benzene radical siloxane, poly- methyl ethylene trifluoropropyl siloxane, vinylidene-chlorotrifluoroethylene, inclined fluorine second Alkene-hexafluoropropylene copolymer, vinylidene-tetrafluoraoethylene-hexafluoropropylene copolymer, tetrafluoroethylene propylene copolymer, polycyclic oxygen Chloropropane, epichlorohydrin ethylene oxide copoymer, epoxychloropropane-ethylene oxide-propylene oxide copolymer etc..

Wherein, the type of other polymers does not limit, mainly depending on required material property；Other used are poly- The dosage for closing object is not particularly limited, generally 1-50wt%.

Wherein, the auxiliary agent may include but be not limited to the combination of following one or more, such as additive synthesis, including catalysis Agent, initiator；Stabilizing additive, including antioxidant, light stabilizer, heat stabilizer, dispersing agent, emulsifier, fire retardant；Improve The auxiliary agent of mechanical property, including toughener, coupling agent；Improve the auxiliary agent of processing performance, including solvent, lubricant, release agent, increasing Mould agent, thickener, thixotropic agent, levelling agent；Change the auxiliary agent of coloured light, including colorant, fluorescent whitening agent, delustering agent；Other are helped Agent, including antistatic agent, biocide mildewcide, foaming agent, foam stabiliser, nucleating agent, rheological agent etc..

Catalyst in the auxiliary agent can reduce reaction activity by changing reaction path to accelerate to react The reaction rate of object during the reaction.It includes but are not limited to following any or appoints several catalyst: 1. polyurethane closes At with catalyst: amines catalyst, such as triethylamine, triethylenediamine, bis- (dimethylaminoethyl) ethers, 2- (2- dimethylamino- Ethyoxyl) ethyl alcohol, trimethyl hydroxyethylammonium propane diamine, N, bis- (dimethylamine propyl) isopropanolamines of N-, N- (dimethylamino-propyl) two Isopropanolamine, N, N, N '-trimethyl-N '-ethoxy diamine ethylether, tetramethyl dipropylenetriamine, N, N- dimethyleyelohexane Amine, N, N, N ', N '-tetramethyl Alkylenediamine, N, N, N ', N ', N '-five methyl diethylentriamine, N, N- dimethyl ethanol Amine, N-ethylmorpholine, 2,4,6- (dimethylamino methyl) phenol, trimethyl-N-2- hydroxypropyl caproic acid, N, N- dimethyl benzylamine, N, N- dimethyl cetylamine etc.；Organometallic catalysts, such as stannous octoate, dibutyltin dilaurate, dioctyl tin two Laurate, zinc Isoocatanoate, isooctyl acid lead, potassium oleate, zinc naphthenate, cobalt naphthenate, ferric acetyl acetonade, phenylmercuric acetate, propionic acid Benzene mercury, bismuth naphthenate, sodium methoxide, potassium octanoate, potassium oleate, calcium carbonate etc.；2. polyolefin catalyst for synthesizing: such as Ziegler- Natta catalyst, π-allyl nickel, alkyl lithium catalyst, metallocene catalyst, aluminium diethyl monochloride, titanium tetrachloride, tri-chlorination Titanium, boron trifluoride etherate, magnesia, dimethylamine, stannous chloride, triethylamine, tetraphenylboron sodium, antimony oxide, sesquialter Ethylmercury chloride aluminium, vanadium oxytrichloride, triisobutyl aluminium, nickel naphthenate, naphthenic acid rare earth etc.；3. CuAAC catalysts: by monovalence Copper compound and amine ligand share concerted catalysis；Monovalence copper compound can be selected from Cu (I) salt, as CuCl, CuBr, CuI, CuCN, CuOAc etc.；Also selected from Cu (I) complex compound, such as [Cu (CH₃CN)₄]PF₆、[Cu(CH₃CN)₄]OTf、CuBr(PPh₃)₃Deng；Amine Ligand can be selected from three [(1- benzyl -1H-1,2,3- triazole-4-yl) methyl] amine (TBTA), three [(1- tert-butyl -1H-1,2,3- Triazole-4-yl) methyl] amine (TTTA), three (2- benzimidazole methyl) amine (TBIA), hydration bathophenanthroline disulfonic acid sodium etc.；④ Thiol-ene catalysts: photochemical catalyst, such as dimethoxybenzoin, 2- hydroxy-2-methyl phenylacetone, 2,2- dimethoxy Base -2- phenyl acetophenone etc.；Nucleopilic reagent catalyst, such as ethylenediamine, triethanolamine, triethylamine, pyridine, 4- dimethylamino pyrrole Pyridine, imidazoles, diisopropyl ethyl amine etc..Catalyst amount used is not particularly limited, generally 0.01-0.5wt%.

Initiator in the auxiliary agent can cause monomer molecule to activate in polymerization process and generate free Base improves reaction rate, and reaction is promoted to carry out, and includes but are not limited to following any or appoints several initiators: 1. free radical Polymerization initiator: organic peroxide, such as lauroyl peroxide, benzoyl peroxide (BPO), dicetyl peroxydicarbonate diisopropyl Bis- (4- tert-butylcyclohexyl) esters of ester, di-cyclohexylperoxy di-carbonate, dicetyl peroxydicarbonate, tert-butyl hydroperoxide benzoic acid Ester, tert-butyl hydroperoxide pivalate, di-tert-butyl peroxide, di-isopropylbenzene hydroperoxide；Azo-compound, such as azo two Isobutyronitrile (AIBN), azobisisoheptonitrile；Inorganic peroxide, such as ammonium persulfate, potassium peroxydisulfate；2. living polymerization causes Agent: such as 2,2,6,6- tetramethyl -1- oxygroup piperidines, 1- chloro-1-phenyl ethane/stannous chloride/bis- pyridines ternary system；3. from Son polymerization initiator: such as butyl lithium, sodium/naphthalene system, boron trifluoride/aqueous systems, tin tetrachloride/alkyl halide system；4. matching Position polymerization initiator: such as titanium tetrachloride/triethyl aluminum system, two zirconium cyclopentadienyl of dichloro/methylaluminoxane system；5. ring-opening polymerisation With initiator: such as sodium methoxide, potassium methoxide, ethylenediamine, hexamethylene diisocyanate, stannous octoate.Wherein, the preferred mistake of initiator Aoxidize lauroyl, benzoyl peroxide, azodiisobutyronitrile, potassium peroxydisulfate.Initiator amount used is not particularly limited, and one As be 0.1-1wt%.

Antioxidant in the auxiliary agent can delay the oxidation process of polymer samples, guarantee that material can be suitable It is processed and is prolonged its service life sharply, include but are not limited to following any or appoint several antioxidant: Hinered phenols, Such as 2,6 di tert butyl 4 methyl phenol, 1,1,3- tri- (- 4 hydroxyl -5- tert-butyl-phenyl of 2- methyl) butane, four [β-(3,5- Di-tert-butyl-hydroxy phenyl) propionic acid] pentaerythritol ester, 2,2 '-di-2-ethylhexylphosphine oxides (4- methyl-6-tert-butylphenol)；Sulfur-bearing by Hinder phenols, such as 4,4 '-thiobis-[3 methy 6 tert butyl phenol], 2,2 '-thiobis-[4- methyl-6-tert-butylphenol]； Triazine system hindered phenol, such as 1,3,5- bis- [β-(3,5- di-tert-butyl-hydroxy phenyl) propionyl]-perhydro-s-triazines；Trimerization isocyanide Acid esters Hinered phenols, such as three (3,5- di-tert-butyl-4-hydroxyl benzyl)-triisocyanates；Amine, such as N, N '-two (betanaphthyl) P-phenylenediamine, N, N '-diphenyl-para-phenylene diamine, N- phenyl-N '-cyclohexyl p-phenylenediamine；Sulfur-bearing class, such as thiodipropionic acid dilauryl Osmanthus ester, 2-mercaptobenzimidazole, 2-mercaptobenzothiazole；Phosphorous acid esters, such as triphenyl phosphite, three nonyl benzene of phosphorous acid Ester, three [2.4- di-tert-butyl-phenyl] phosphite esters etc.；Wherein, the preferred tea polyphenols of antioxidant (TP), butylated hydroxy anisole (BHA), dibutyl hydroxy toluene (BHT), tert-butyl hydroquinone (TBHQ), three [2.4- di-tert-butyl-phenyl] phosphite esters (irgasfos 168), four [β-(3,5- di-tert-butyl-hydroxy phenyl) propionic acid] pentaerythritol esters (antioxidant 1010).Used Antioxidant dosage is not particularly limited, generally 0.01-1wt%.

Light stabilizer in the auxiliary agent can prevent polymer samples from light aging occurs, prolong its service life, It includes but are not limited to following any or appoints several light stabilizers: photomask agent, such as carbon black, titanium dioxide, zinc oxide, sulfurous Sour calcium；Ultraviolet absorbing agent, such as ESCALOL 567,2-hydroxy-4-n-octoxybenzophenone, 2- (2- hydroxyl Base -3,5- di-tert-butyl-phenyl) -5- chlorobenzotriazole, 2- (2- hydroxy-5-methyl base phenyl) benzotriazole, (the 2- hydroxyl of 2,4,6- tri- Base -4- n-butoxyphenyl) -1,3,5- s-triazine, 2- cyano -3,3- diphenylacrylate 2- ethylhexyl；Pioneer's type is ultraviolet Light absorbers, such as the p- tert-butyl phenyl ester of salicylic acid, double acid double phenol A ester；UV quenchers, such as bis- (3,5- bis- tertiary fourths Base -4- benzylphosphonic acid mono ethyl ester), 2,2 '-thiobis (4- spy's octyl phenol oxygroup) nickel；Hindered amine light stabilizer, such as the last of the ten Heavenly stems two Bis- (2,2,6,6- tetramethyl piperidine) esters of acid, benzoic acid (2,2,6,6- tetramethyl piperidine) ester, three (1,2,2,6,6- pentamethyl piperazines Piperidinyl) phosphite ester；Other light stabilizers, such as 3,5- di-tert-butyl-4-hydroxybenzoic acid (2,4- di-tert-butyl) ester, alkyl Phosphoamide, N, N '-zinc dibutyl dithiocaarbamate, N, positive fourth positive group aminodithioformic acid nickel of N '-two etc.；Its In, bis- (2,2,6, the 6- tetramethyl piperidine) esters (light stabilizer 770) of the preferred carbon black of light stabilizer, decanedioic acid.Light used is stablized Agent dosage is not particularly limited, generally 0.01-0.5wt%.

Heat stabilizer in the auxiliary agent enables to polymer samples in processing or use process not due to heated Chemical change occurs, or delays these variations to achieve the purpose that prolong the service life comprising but it is not limited only to following A kind of or several heat stabilizers: lead salts, such as lead sulfate tribasic, dibasic lead phosphite, dibasic lead stearate, disalt Base phthalic acid lead, tribasic Malaysia lead plumbate, slag lead silicate, lead stearate, lead salicylate, dibasic phthalic acid Lead, basic lead carbonate, silica gel are co-precipitated lead silicate；Metal soap: such as cadmium stearate, barium stearate, calcium stearate, stearic acid Lead, zinc stearate；Organo-tin compound class, such as di-n-butyltin dilaurate, Bis(lauroyloxy)dioctyltin, maleic acid two (just) butyl tin, double single-ethylhexyl maleate dioctyltins, dimercapto 2-ethyl hexyl ethanoate dioctyltin, capital tin C-102, two mercaptos Guanidine-acetic acid isooctyl stannous methide, two mercaptan stannous methides and its compound；Antimony stabilizer, such as mercaptan antimonic salt, mercaptoacetate Mercaptans type, mercapto-carboxylic ester antimony, carboxylate antimony；Epoxy compound species, such as epoxidized oil, epoxy aliphatic ester, epoxy resin；It is sub- Phosphoric acid ester, such as three aromatic ester of phosphorous acid, three alkyl ester of phosphorous acid, three aralkyl ester of phosphorous acid, alkane virtue mixed ester, aggretion type phosphorous acid Ester；Polyalcohols, such as pentaerythrite, xylitol, mannitol, D-sorbite, trimethylolpropane；Composite thermal stabilizer, such as altogether Precipitate metallic soap, liquid metal soap compound stabilizer, organotin compound stabilizer etc.；Wherein, the preferred barium stearate of heat stabilizer, Calcium stearate, di-n-butyltin dilaurate, maleic acid two (just) butyl tin.Heat stabilizer dosage used does not limit especially It is fixed, generally 0.1-0.5wt%.

Dispersing agent in the auxiliary agent enables to solid flocculation group in mixed with polymers liquid to be separated into tiny particle And be suspended in liquid, those are poorly soluble the solid and liquid particles in liquid for uniform dispersion, while can also prevent particle Sedimentation and cohesion form stable suspension comprising but be not limited only to following any or appoint several dispersing agents: anionic, Such as alkylsurfuric acid ester sodium salt, sodium alkyl benzene sulfonate, petroleum sodium sulfonate；Cationic；It is non-ionic, such as aliphatic alcohol polyethenoxy Ether, sorbitol anhydride fatty acid polyoxyethylene ether；Inorganic type, such as silicate, condensed phosphate；Polymer electrolyte, such as starch, bright Glue, water-soluble glue, lecithin, carboxymethyl cellulose, hydroxyethyl cellulose, sodium alginate, lignosulfonates, polyvinyl alcohol Deng.Wherein, the preferred neopelex of dispersing agent, naphthalene system methylene sulfonate (dispersing agent N), aliphatic alcohol polyethenoxy Ether, dispersant dosage used are not particularly limited, generally 0.3-0.8wt%.

Emulsifier in the auxiliary agent can improve in the mixed with polymers liquid comprising auxiliary agent between various composition phases Surface tension is allowed to form uniform and stable dispersion or emulsion comprising but be not limited only to following any or appoint several Kind emulsifier: anionic, such as higher fatty acid salt, alkylsulfonate, alkylbenzene sulfonate, Negel, succinic acid Sulfonated ester, petroleum sulfonate, aliphatic alcohol sulfate, castor oil salt, sulphation butyl ricinoleate salt, phosphate ester salt, Fatty acyl-peptide condensation product；Cationic, such as alkylammonium salt, alkyl quaternary ammonium salts, Fixanol；Amphoteric ion type, such as carboxylate Type, sulfonic acid ester type, sulfuric acid ester type, phosphate type；It is non-ionic, such as fatty alcohol polyoxyethylene ether, alkyl phenol polyoxyethylene ether, rouge Fat acid polyoxyethylene ester, polypropylene oxide-ethylene oxide adduct, fatty acid glyceride, pentaerythritol fatty ester, sorbierite And sorbitan fatty acid ester, sucrose fatty ester, hydramine fatty acid amide etc..Wherein, preferably neopelex, lose Water Span, triethanolamine stearate (Emulphor FM), emulsifier used are not particularly limited, generally For 1-5wt%.

Fire retardant in the auxiliary agent can increase the flame resistance of material comprising but be not limited only to following any Or appoint several fire retardants: phosphorus system, such as red phosphorus, tricresyl phosphate, triphenyl phosphate, tricresyl phosphate, tricresyl phosphate hexichol Ester；Halogen phosphoric acid ester, such as three (2,3- dibromopropyl) phosphates, tricresyl phosphate (2,3- dichloro the third) ester；Organohalogen compounds are such as high Chlorinty chlorinated paraffin, 1,1,2,2- tetrabromoethane, deca-BDE, penta decane of perchloro- ring；Inorganic fire retardants, such as three oxidations two Antimony, aluminium hydroxide, magnesium hydroxide, zinc borate；Reactive flame retardant, such as chlorendic anhydride, bis- (2,3- dibromopropyl) anti-butylene two Acid esters, tetrabromobisphenol A, tetrabromophthalic anhydride etc.；Wherein, the preferred deca-BDE of fire retardant, triphenyl phosphate, tricresyl phosphate Toluene ester, phosphate toluene diphenyl ester, antimony oxide.Amount of flame-retardant agent used is not particularly limited, generally 1-20wt%.

Toughener in the auxiliary agent can reduce polymer samples brittleness, increase toughness, and it is strong to improve material carrying Degree comprising but be not limited only to following any or appoint several toughener: methyl methacrylate-butadiene-styrene copolymerization Resin, chlorinated polyethylene resin, ethylene-vinyl acetate copolymer resin and its modifier, acrylonitrile-butadiene-benzene second Alkene copolymer, acrylonitrile-butadiene copolymer, the third glue of second, ethylene-propylene diene copolymer, cis-butadiene cement, butadiene-styrene rubber, styrene-butadiene-benzene Ethylene block copolymer etc.；Wherein, preferred the third glue of second of toughener, acrylonitrile-butadiene-styrene copolymer (ABS), benzene second Alkene-butadiene-styrene block copolymer (SBS), Methyl Methacrylate-Butadiene-Styrene Copolymer resin (MBS), Chlorinated polyethylene resin (CPE).Toughener dosage used is not particularly limited, generally 5-10wt%.

Coupling agent in the auxiliary agent can improve the interface characteristics of polymer samples and inorganic filler or reinforcing material Can, the viscosity of material melt is reduced in plastic processes, improves the dispersion degree of filler to improve processing performance, and then make to make Product obtain good surface quality and machinery, heat and electrical property comprising but be not limited only to following any or appoint several couplings Agent: chromium of organic acid complex compound, silane coupling agent, titanate coupling agent, sulfonyl azide coupling agent, aluminate coupling agent etc.；Wherein, The preferred gamma-aminopropyl-triethoxy-silane of coupling agent (Silane coupling agent KH550), γ-(the third oxygen of 2,3- epoxy) propyl trimethoxy Base silane (silane coupling agent KH560).Coupling agent dosage used is not particularly limited, generally 0.5-2wt%.

Solvent in the auxiliary agent, adjustable viscosity are convenient for technological operation, make in product preparation process or in preparing With.Its include but are not limited to it is following any or appoint it is several: hydro carbons (such as hexamethylene, heptane), halogenated hydrocarbon (such as methylene chloride, Chloroform, tetrachloromethane), aromatic hydrocarbons (such as toluene, dimethylbenzene), ketone (such as acetone, methyl ethyl ketone), ethers (such as ether, tetrahydro furan Mutter, dioxane), esters (such as ethyl acetate, butyl acetate), glycol ether-ether (such as ethylene glycol ether acetate, propylene glycol list first Ether acetate), dimethylformamide (DMF), N-Methyl pyrrolidone (NMP) etc..Solvent usage used is not particularly limited, Generally 1-200wt%.

Lubricant in the auxiliary agent can be improved the lubricity of polymer samples, reduce friction, reduce Interface Adhesion Performance comprising but be not limited only to following any or appoint several lubricants: saturated hydrocarbons and halogenated hydrocarbon, such as solid paraffin, micro- Spar wax, atoleine, low molecular weight polyethylene, oxidized polyethylene wax；Fatty acid, such as stearic acid, hydroxy stearic acid；Fat Esters of gallic acid, such as fatty acid low-carbon-ester, polyol esters of fatty acids, native paraffin, ester type waxes and saponified wax；Aliphatic amide type is such as hard Acyl amine or stearic amide, oleamide or oleamide, erucyl amide, N, N '-ethylene bis stearamide；Fatty alcohol and polynary Alcohols, such as stearyl alcohol, cetanol, pentaerythrite；Metal soap, as lead stearate, calcium stearate, barium stearate, magnesium stearate, Zinc stearate etc.；Wherein, the preferred solid paraffin of lubricant, atoleine, stearic acid, low molecular weight polyethylene.Lubrication used Agent dosage is not particularly limited, generally 0.5-1wt%.

Release agent in the auxiliary agent, it can make polymer samples be easy to demould, and surface is smooth, clean comprising but It is not limited only to following any or appoints several release agents: paraffin hydrocarbon, soaps, dimethicone, ethyl silicon oil, aminomethyl phenyl silicon Oil, castor oil, used oil, mineral oil, molybdenum disulfide, polyethylene glycol, vinyl chloride resin, polystyrene, silicon rubber, polyvinyl alcohol Deng；Wherein, the preferred dimethicone of release agent, polyethylene glycol.Release agent dosage used is not particularly limited, generally 0.5- 2wt%.

Plasticizer in the auxiliary agent can increase the plasticity of polymer samples, so that the hardness of polymer, mould Amount, softening temperature and brittle temperature decline, elongation, flexibility and flexibility improve comprising but be not limited only to following any Kind appoints several plasticizer: Phthalates: dibutyl phthalate, dioctyl phthalate, phthalic acid two Different monooctyl ester, dibutyl phthalate (DHP), diisooctyl phthalate, diisononyl phthalate, phthalic acid fourth benzyl Bis- (13) esters of ester, butyl phthalate butyl glycolate, dicyclohexyl phthalate, phthalic acid, terephthaldehyde Sour two (2- ethyl) own esters；Phosphoric acid ester, such as tricresyl phosphate, phosphoric acid (hexichol -2- ethyl) own ester；Fatty acid ester, such as The own ester of adipic acid two (2- ethyl), decanedioic acid two (2- ethyl) own ester；Epoxy compound species, such as epoxy glycerite esters, epoxy rouge Fatty acid monoester class, epoxy tetrahydrophthalic acid esters, epoxidized soybean oil, the own ester of epoxystearic acid (2- ethyl), epoxy soybean Oleic acid 2- ethylhexyl, the own ester of 4,5- epoxy tetrahydrophthalic acid two (2- ethyl), Chinese littleleaf box methyl acetylricinolate, binary Alcohol lipid, such as the sour glycol ester of C5~9, the sour Triethylene Glycol of C5~9；Class containing chlorine such as afforests paraffin class, chlorinated fatty acid Ester；Polyesters, such as ethanedioic acid 1,2-PD system polyester, decanedioic acid 1,2-PD polyester；Phenyl alkylsulfonate, trimellitic acid Ester, citrate, pentaerythrite and pentaerythritol fatty acid ester etc.；Wherein, plasticizer pref-erable dioctyl phthalate (DOP), neighbour Dibatyl phithalate (DBP), diisooctyl phthalate (DIOP), diisononyl phthalate (DINP), adjacent benzene two Formic acid diisodecyl ester (DIDP), tricresyl phosphate (TCP).Plasticizer consumption used is not particularly limited, generally 5- 20wt%.

Thickener in the auxiliary agent, can assign the good thixotropy of mixed with polymers liquid and consistency appropriate, and one As used during production of the invention and semi-finished product store comprising but be not limited only to following any or appoint several thickenings Agent: lower-molecular substance, such as fatty acid salt, fatty alcohol polyoxyethylene ether sulfate, alkyldimethylamine oxide, fatty acid monoethanol Amide, fatty diglycollic amide, fatty acid Isopropamide, anhydro sorbitol tricarboxylic ester, glycerol trioleate, coconut monoethanolamide Propyl betaine, 2- alkyl-N- carboxymethyl-N- hydroxyethyl imidazole quinoline, titanate coupling agent；Polymer substance, such as bentonite, manually Hectorite, fine particle silica, colloidal aluminum, plant polyose class, microbial polysaccharide class, animal protein, cellulose family, starch, Seaweed acids, poly-methyl acrylate, methacrylic acid copolymer, cis-butenedioic anhydride copolymer, crotonic acid-copolymers, polyacrylamide, Polyvinyl pyrrolidone, polyvinyl alcohol, polyethers, polyvinyl methyl ether urethane polymer etc.；Wherein, the preferred hydroxy ethyl fiber of thickener Element, coconut oil diethanol amide, acrylic acid-methacrylic acid copolymer.Thickener dosage used is not particularly limited, generally For 0.1-1.5wt%.

Thixotropic agent in the auxiliary agent is added in polymeric system, increases the thixotropy of polymeric system.Including but not It is only limitted to following any or appoints several: gas-phase silica, rilanit special, bentonite, silicic acid anhydride, silica derivative, urea Derivative etc..Thixotropic agent dosage used is not particularly limited, generally 0.5-2wt%.

Levelling agent in the auxiliary agent can guarantee the flat and smooth uniform of polymer coating film, improve film coated surface matter Amount improves dicoration comprising but be not limited only to following any or appoint several levelling agents: dimethyl silicone polymer, poly- methyl Phenyl siloxane, cellulose acetate butyrate, polyacrylate, organic siliconresin etc.；Wherein, the preferred poly dimethyl of levelling agent Siloxanes, polyacrylate.Levelling agent dosage used is not particularly limited, generally 0.5-1.5wt%.

Colorant in the auxiliary agent can make polymeric articles show required color, increase surface color and polish, It includes but are not limited to following any or appoints several colorants: inorganic pigment, such as titanium white, chrome yellow, cadmium red, iron oxide red, molybdenum chromium Red, ultramarine, chrome green, carbon black；Organic pigment, such as lithol red BK directions, lake red C, red, good base R is red, phthalocyanine is red, Yong Guyang The bright red R of red HF3C, the plastics and not red BR of Crow, forever solid orange HL, Fast Yellow G, vapour bar plastics Huang R, permanent yellow 3G, permanent yellow H2G, Phthalocyanine blue B, dark green, plastics purple RL, nigrosine；Organic dyestuff, such as thioindigo red, vat yellow 4GF, indanthrene blue RSN, slag rose Rare essence, Oil Yellow etc.；Wherein, the selection of colorant does not need to be particularly limited to depending on color sample demand.Coloring used Agent dosage is not particularly limited, generally 0.3-0.8wt%.

Fluorescent whitening agent in the auxiliary agent can make contaminated substance obtain the sparkling effect of similar fluorite, It includes but are not limited to following any or appoints several fluorescent whitening agents: Stilbene-based, coumarin type, pyrazoline type, benzo Oxygen nitrogen type, phthalimide type etc.；Wherein, the preferred stilbene biphenyl sodium disulfonate (fluorescent whitening agent of fluorescent whitening agent CBS), bis- (5 methyl -2- benzoxazolyl) talan (fluorescent whitening agent KSN) of 4,4-, 2,2- (4,4 '-diphenylethyllene) Double benzoxazoles (fluorescent whitening agent OB -1).Fluorescent whitening agent dosage used is not particularly limited, generally 0.002- 0.03wt%.

Delustering agent in the auxiliary agent when incident light being enabled to reach polymer surfaces, occurs diffusing reflection, generates low The matt and delustring appearance of gloss comprising but be not limited only to following any or appoint several delustering agents: sedimentation barium sulfate, dioxy SiClx, aqueous gypsum powder, talcum powder, titanium dioxide, poly- methyl carbamide resin etc.；Wherein, the preferred silica of delustering agent.Used disappears Photo etching dosage is not particularly limited, generally 2-5wt%.

The deleterious charge assembled in polymer samples can be guided or be eliminated, make it by the antistatic agent in the auxiliary agent Production and life are not brought inconvenience or are endangered comprising but be not limited only to following any or appoint several antistatic agents: yin from Subtype antistatic agent, such as alkylsulfonate, to Sodium Nonylphenoxypropane Sulfonate, alkyl phosphate diethanolamine salt, alkyl phenol Polyoxyethylene groups ether sulfonic acid triethanolamine, to nonyl diphenyl ether potassium sulfonate, alkyl polyoxyethylene base ether sulfonic acid triethanolamine, phosphoric acid Ester derivant, phosphate, phosphoric acid polyethylene oxide alkyl ethers alcohol ester, alkyl bis- [two (2- ethylol amine)] phosphates, phosphate Derivative, fatty amine sulfonate, butyrate sodium sulfonate；Cationic antistatic agent, such as aliphatic ammonium salt hydrochlorate, lauryl trimethyl Ammonium chloride, dodecyl trimethylamine bromide, N, N- cetyl-ethyl morpholine ethyl-sulfate salt, stearamide propyl (2- hydroxyl second Base) dimethylammonium nitrate, alkyl hydroxyethyl dimethylammonium perchlorate, 2- alkyl -3,3- dihydroxy ethyl imidazoline perchlorate, 2- Heptadecyl -3- ethoxy -4- carboxymethyl imidazoline, N, bis- (α-ethoxy)-N-3 (dodecyloxy -2- hydroxypropyl) first of N- Ammonium Methylsulfate salt；Amphoteric ion type antistatic agent, such as alkyl dicarboxyl methyl ammonium second inner salt, lauryl betaine, N, N, N- tri- Alkylammonium acetyl (N '-alkyl) amine second inner salt, bis- polyethylene oxide base-N- ethylphosphonic acid sodium of N- lauryl-N, N-, alkyl two Salt hydroxide, -3 ethoxy -3- acetic acid alkali imidazoline quaternary amine alkali of 2- alkyl, N- alkyl amino acid in (polyoxyethylene) ammonium second Salt；Non-ionic antistatic agent, such as fatty alcohol ethylene oxide adduct, fatty acid ethylene oxide addition product, alkyl phenol epoxy second The polyethylene oxide of alkane addition product, tricresyl phosphate polyoxyethylene groups ether-ether, fatty acid monoglyceride, sorbitan mono-laurate Addition product；Polymer Antistatic Agent, ethylene oxide propylene oxide addition product, polyethylene glycol-terephthalic acid (TPA) such as ethylenediamine Ester -3,5- dibenzoate sodium sulfonate copolymers, polyene propionamide N- quaternary ammonium salt substituent, poly- 4- vinyl -1- acetonyl pyrrole Pyridine phosphoric acid-is to butyl phenyl ester salt etc.；Wherein, the preferred lauryl trimethyl ammonium chloride of antistatic agent, octadecyldimethyl hydroxyl second Base quaternary ammonium nitrate (antistatic agent SN), alkyl phosphate diethanolamine salt (antistatic agent P).Antistatic agent dosage used does not have It is particularly limited to, generally 0.3-3wt%.

Dehydrating agent in the auxiliary agent, can moisture in removing system comprising but be not limited only to it is following any or Appoint several: oxazolidine compound (such as 3- Ethyl-2-Methyl -2- (3- methyl butyl) -1,3- oxazolidine), different to Methyl benzenesulfonyl Cyanate, triethyl orthoformate, vinyl silanes, calcium oxide etc..Dehydrating agent dosage used is not particularly limited, generally 0.1-2wt%.

Biocide mildewcide in the auxiliary agent can inhibit the growth of bacterium, and the appearance for keeping product clean and tidy extends and uses Service life；Or protection user, the health for promoting user, such as reduce tinea pedis.It includes organic matter and inorganic matter, including but It is not limited only to following any or appoints several: isothiazolinone derivatives, such as 5-Chloro-2-methyl-4-isothiazolin-3-one, 2- Methyl -4- isothiazoline -3- ketone, N- normal-butyl -1,2- benzisothiazole-3-ketone, octylisothiazolinone, 2,4,4- tri- Chlorine-2-hydroxyl-diphenyl ether, 2- (4- thiazolyl) benzimidazole, copper 8-quinolinolate or bis- (8-hydroxyquinoline base) copper；It is organic Tin compound, such as tributyl-tin fumarate, tributyltin acetate, bis- (tributyl tin) sulfide, bis- (tributyl tin) tin oxide； N, N- dimethyl-N '-phenyl (fluorine dichloromethyl is thio) sulfonamide；Inorganic compound or compound, such as nano silver, nano-silica Change titanium, nano silica, nano zine oxide, superfine cupper powder, inorganic antiseptic YY-Z50, XT inorganic antiseptic, composite antibacterial Agent KHFS-ZN.Biocide mildewcide dosage used is not particularly limited, generally 0.5-2wt%.

Foaming agent in the auxiliary agent can make polymer samples foaming pore-forming, to obtain light polymeric material Material comprising but be not limited only to it is following any or appoint several foaming agents: physical blowing agent, as carbon dioxide, nitrogen, argon gas, Methane, ethane, propane, butane, iso-butane, pentane, neopentane, hexane, isopentane, heptane, isoheptane, acetone, benzene, toluene, Methyl ether, ether, petroleum ether, chloromethanes, methylene chloride, dichloroethylene, dicholorodifluoromethane, trifluorochloromethane, hydrochlorofluorocarbons- 22, hydrochlorofluorocarbons -142b, hydrofluorocarbons -134a, hydrofluorocarbons -152a, chlorofluorocarbons -11, chlorofluorocarbons -12, chlorine fluorine Hydrocarbon -114；Inorganic foaming agent, such as sodium bicarbonate, ammonium carbonate, ammonium hydrogen carbonate, carbonate ammonia natrium, azido compound, hydroboron Deng；Organic foaming agent, such as N, N '-dinitrosopentamethlyene tetramine, N, N '-dimethyl-N, N '-dinitroso paraphenylene terephthalamide Amine, azodicarbonamide, barium azo-biscarbonate, two diisopropyl carbonate of azo, azodicarbonamide potassium formate, two isobutyl of azo Nitrile, 4,4 '-oxobenzenesulfonyl hydrazide, 3,3 '-disulfonyl hydrazide diphenyl sulphone (DPS)s, 1,3- benzene Erhuang hydrazides, benzene sulfonyl hydrazide, three diazanyls three Piperazine, p-toluene sulfonylsemicarbazide, biphenyl -4,4 '-disulfonyl nitrine, diazo aminobenzene；Physical microballoon/granule foaming agent, such as The expandable microballoon of the companies such as Akzo Nobel production.Wherein, the preferably environmentally friendly carbon dioxide of foaming agent, nitrogen, argon Gas and sodium bicarbonate, ammonium carbonate, azodicarbonamide (blowing agent AC), N, five methine tetramine (foaming agent of N '-dinitro H), N, N '-dimethyl-N, N '-dinitrosoterephthalamine (foaming agent NTA), physical microballoon foaming agent.Hair used Infusion dosage is not particularly limited, generally 0.1-30wt%.

Blowing promotor in the auxiliary agent comprising but be not limited only to foamed promoter, frothing inhibitor, foam and stablize Agent etc..The foamed promoter comprising but be not limited only to it is following any or appoint it is several: urea, stearic acid, lauric acid, Salicylic acid, tribasic lead sulfate, dibasic lead phosphite, lead stearate, cadmium stearate, zinc stearate, zinc oxide, ZB- 530,KZ-110,MS-1；The frothing inhibitor comprising but be not limited only to following any or appoint several: maleic acid, richness Horse acid, stearyl chloride, phthalyl chloride, maleic anhydride, phthalate anhydride, hydroquinone, naphthalenediol, aliphatic amine, amide, Oxime, isocyanates, mercaptan, thiophenol, thiocarbamide, sulfide, sulfone, cyclohexanone, acetylacetone,2,4-pentanedione, hexacholorocyclopentadiene, dibutyl Malaysia Sour tin etc.；The foam stabiliser comprising but be not limited only to it is following any or appoint it is several:: silicone oil, sulfonated aliphatic alcohol, Alpha-sulfonated fatty acid, NaLS, dodecyldimethylamine oxide, alkylolamides, polyethylene glycol oxide, alkylaryl are poly- Ethylene oxide alcohol, tridecyl ether, Polyoxyethylene sorbitan glycerol monolaurate, siloxanes-ethylene oxide are embedding Section copolymer etc..Blowing promotor dosage used is not particularly limited, generally 0.05-10wt%.

Nucleating agent in the auxiliary agent can accelerate crystalline rate, increase knot by the crystallization behavior of change polymer Brilliant density and promote fine grain size, reach and shorten material molding cycle, improves the product transparency, lustrous surface, tension The purpose of the physical mechanical properties such as intensity, rigidity, heat distortion temperature, impact resistance, creep resistance comprising but be not limited only to Under it is any or appoint several nucleating agents: benzoic acid, adipic acid, sodium benzoate, talcum powder, p-phenolsulfonic acid's sodium, silica, two Benzal D-sorbite and its derivative, EP rubbers, ethylene propylene diene rubber etc.；Wherein, the preferred silica of nucleating agent, two benzals D-sorbite (DBS), ethylene propylene diene rubber.Nucleating agent dosage used is not particularly limited, generally 0.1-1wt%.

Rheological agent in the auxiliary agent can guarantee that polymer has good brushability and appropriate during film Coating thickness, the sedimentation of solid particle, can be improved its redispersibility comprising but be not limited only to following when preventing storage A kind of or several rheological agents: inorganic, such as barium sulfate, zinc oxide, alkaline earth oxide, calcium carbonate, lithium chloride, sulfuric acid Sodium, magnesium silicate, fumed silica, waterglass, colloidal silicon dioxide；Organo-metallic compound, as aluminum stearate, aluminium alkoxide, Titanium chelate, aluminium chelate compound；Organic, such as organobentonite, rilanit special/amide waxe, isocyanate derivates, acrylic acid Lotion, acrylic copolymer, polyethylene wax, cellulose esters etc.；Wherein, the preferred organobentonite of rheological agent, polyethylene wax, hydrophobic Modified alkaline swellable emulsions (HASE), alkali-swellable emulsions (ASE).Rheological agent dosage used is not particularly limited, and one As be 0.1-1wt%.

The filler primarily serves following effect in polymer samples: 1. reducing the shrinking percentage of molded article, mentions Dimensional stability, surface smoothness, flatness and the zero diopter of high product or without photosensitiveness etc.；2. adjusting the viscosity of material；③ Meet different performance requirement, such as improves material impact intensity and compressive strength, hardness, rigidity and modulus, improve wearability, improve Heat distortion temperature improves electric conductivity and thermal conductivity etc.；4. improving the coloring effect of pigment；5. assigning photostability and chemically-resistant being rotten Corrosion；6. playing compatibilization, cost can be reduced, improves product competitiveness in the market.

The filler, selected from following any or appoint several fillers: inorganic non-metallic filler, organic is filled out at metal packing Material.

The inorganic non-metallic filler includes but are not limited to following any or appoints several: calcium carbonate, clay, sulphur It is sour barium, calcium sulfate and calcium sulfite, talcum powder, white carbon black, quartz, mica powder, clay, asbestos, asbestos fibre, orthoclase, white Chalk, lime stone, blanc fixe, gypsum, graphite, carbon black, graphene, graphene oxide, fullerene, carbon nanotube, molybdenum disulfide, Slag, flue dust, wood powder and shell powder, diatomite, red mud, wollastonite, silica-alumina carbon black, aluminium hydroxide, magnesium hydroxide, flyash, Oil shale powder, swelling perlite powder, aluminum nitride powder, boron nitride powder, vermiculite, iron cement, white clay, alkali mud, boron mud, glass microballoon, tree Rouge microballon, glass powder, cement, glass fibre, carbon fiber, quartz fibre, charcoal core boron fibre, titanium diboride fiber, calcium titanate are fine Dimension, silicon carbide fibre, ceramic fibre, whisker etc..In an embodiment of the invention, preferably conductive inorganic non- Metal packing includes but are not limited to graphite, carbon black, graphene, carbon nanotube, carbon fiber, facilitates and obtains electric conductivity and/or tool There is the composite material of electric heating function.In yet another embodiment of the present invention, preferably have and make in infrared and/or near infrared light With the lower non-metallic fillers with heating function, graphene, graphene oxide, carbon nanotube are included but are not limited to, is conveniently obtained Obtain the composite material heated using infrared and/or near infrared light.Good heating property, the especially fever of remote control property Performance help to obtain the performances such as controllable shape memory, selfreparing.In yet another embodiment of the present invention, preferably have There is the inorganic non-metallic filler of thermal conductivity, includes but are not limited to graphite, graphene, carbon nanotube, aluminium nitride, boron nitride, carbon SiClx facilitates the composite material for obtaining thermally conductive function.

The metal packing, including metallic compound include but are not limited to following any or appoint several: metal powder End, fiber comprising but it is not limited only to copper, silver, nickel, iron, gold etc. and its powder, the fiber of alloy；Nano-metal particle, packet Include but be not limited only to nanogold particle, nano-Ag particles, nanoparticle palladium, nano iron particles, nano cobalt granule, nano nickel Grain, nanometer Fe₃O₄Particle, nanometer γ-Fe₂O₃Particle, nanometer MgFe₂O₄Particle, nanometer MnFe₂O₄Particle, nano Co Fe₂O₄? Grain, nano Co Pt₃Particle, nanometer Fe Pt particle, nanometer Fe Pd particle, ferronickel bimetallic magnetic nanoparticle and other red Outside, near-infrared, ultraviolet, the nano-metal particle that can be generated heat under at least one effect of electromagnetism etc.；Liquid metal comprising but not It is only limitted to mercury, gallium, gallium indium liquid alloy, gallium indium tin liquid alloy, other gallium base liquid metal alloys；Metallo-organic compound point Son, crystal and other in infrared, near-infrared, ultraviolet, the substance that can be generated heat under at least one effect of electromagnetism etc..In the present invention An embodiment in, can preferably carry out electromagnetism and/or near-infrared heating filler, include but are not limited to nanogold, Nano silver, Technique of Nano Pd, nanometer Fe₃O₄, to carry out remote sensing heating.In yet another embodiment of the present invention, preferably liquid is golden Belong to filler, the flexibility and ductility of substrate can be kept while enhancing the thermally conductive of flexible parent metal, electric conductivity.In the present invention Another embodiment in, preferably in infrared, near-infrared, ultraviolet, the organic gold that can generate heat under at least one effect of electromagnetism Belong to compound molecule, crystal, on the one hand facilitates compound, another side raising induction is generated heat efficiency and promote heating effect.

The organic filler includes but are not limited to following any or appoints several: 1. natural organic filler, such as natural Rubber, cotton, velveteen, fiber crops, jute, flax, asbestos, cellulose, cellulose acetate, lignin, starch, wood powder etc.；2. synthesizing Resin extender, such as AAS acrylonitrile acryloid styrene, acrylonitrile-butadiene-styrene copolymer, acetate fiber Element, polytrifluorochloroethylene, haloflex, chliorinated polyvinyl chloride, epoxy resin, ethylene-propylene copolymer, ethylene-acetate second Enoate copolymer, high density polyethylene (HDPE), high impact polystyrene, low density polyethylene (LDPE), medium density polyethylene, melamine-first Urea formaldehyde, polyamide, polyacrylic acid, polyacrylamide, polyacrylonitrile, polyarylsulfone (PAS), polybenzimidazoles, poly terephthalic acid fourth two Alcohol ester, polycarbonate, dimethyl silicone polymer, polyethylene glycol, polyester, polysulfones, polyether sulfone, polyethylene terephthalate, Phenolic resin, tetrafluoroethylene-perfluoro propane copolymer, polyimides, polymethyl acrylate, polymethacrylonitrile, poly- methyl-prop E pioic acid methyl ester, polypropylene, polyphenylene sulfide, polyphenylsulfone, polystyrene, polytetrafluoroethylene (PTFE), polyurethane, polyvinyl alcohol, gathers polyphenylene oxide Vinyl acetate, polyvinyl butyral, polyvinyl chloride, vinyl chloride vinyl acetate copolymer, Vingon, polyethylene Alcohol formal, polyvinylpyrrolidone, Lauxite, ultra-high molecular weight polyethylene, unsaturated polyester (UP), polyether-ether-ketone etc.；3. closing At gum filler, as isoprene rubber, butadiene rubber, butadiene-styrene rubber, nitrile rubber, neoprene, butyl rubber, EP rubbers, Silicon rubber, fluorubber, lactoprene, polyurethane rubber, epichlorohydrin rubber, thermoplastic elastomer (TPE) etc.；4. synthetic fibers are filled out Material, such as viscose fiber, copper ammonia fiber, diethyl ester fiber, triethyl fiber, Fypro, polycarbonate, polyvinyl alcohol Fiber, polyester fiber, polyurethane fiber, polyacrylonitrile fibre, vinylon, polyvinyl chloride fibre, polyolefin are fine Dimension, fluorofibre, polytetrafluoroethylene fibre, aromatic polyamide fibre, aramid fiber or aramid fiber etc.；5. foamed polymer Composition granule and expandable polymer beads.

Wherein, wire feeding does not limit, mainly depending on required material property.Amount of filler used is without spy It does not limit, generally 1-30wt%.

Wherein, the sweller may include but be not limited to water, organic solvent, ionic liquid, oligomer, plasticizer.Its In, oligomer can also be considered as plasticizer.

Organic solvent in the sweller is selected from as an example and includes but is not limited to any of the following or appoint several Kind: hydro carbons (such as hexamethylene, heptane), halogenated hydrocarbon (such as methylene chloride, chloroform, tetrachloromethane), aromatic hydrocarbons (such as toluene, dimethylbenzene), Ketone (such as acetone, methyl ethyl ketone), ethers (such as ether, tetrahydrofuran, dioxane), esters (such as ethyl acetate, acetic acid fourth Ester), glycol ether-ether (such as ethylene glycol ether acetate, propylene glycol monomethyl ether acetate), dimethylformamide (DMF), N- methyl Pyrrolidones (NMP) etc..

Ionic liquid in the sweller is generally made of organic cation and inorganic anion, as an example, sun It includes but is not limited to that alkyl quaternary ammonium ion, alkyl quaternary are seen imidazol ion, the N- alkyl that ion, 1,3- dialkyl group replace that ion, which is selected from, Substituted pyridinium ion etc.；Anion be selected from include but is not limited to for halide ion, tetrafluoroborate ion, hexafluoro-phosphate radical from Son also has CF₃SO₃ ^-、(CF3SO₂)₂N^-、C₃F₇COO^-、C₄F₉SO₃ ^-、CF₃COO^-、(CF₃SO₂)₃C^-、(C₂F₅SO₂)₃C^-、 (C₂F₅SO₂)₂N^-、SbF₆ ^-、AsF₆ ^-Deng.In ionic liquid used in the present invention, the preferred glyoxaline cation of cation, anion It is preferred that hexafluorophosphoricacid acid ions and tetrafluoroborate ion.

Oligomer in the sweller is selected from as an example and includes but is not limited to any of the following or appoint several: Polyethylene glycol oligomer, polyvinyl alcohol oligomer, polyvinyl acetate ester oligomer, polyacrylic acid N-butyl oligomer, liquid stone Wax etc..

Plasticizer in the sweller is selected from as an example and includes but is not limited to any of the following or appoint several: Phthalates: dibutyl phthalate (DBP), dioctyl phthalate (DOP), diisooctyl phthalate (DIOP), dibutyl phthalate (DHP), diisooctyl phthalate (DIDP), diisononyl phthalate (DINP), neighbour Phthalic acid butyl benzyl, butyl phthalate butyl glycolate, dicyclohexyl phthalate, phthalic acid are bis- (13) Ester, terephthalic acid (TPA) two (2- ethyl) own ester；Phosphoric acid ester, as tricresyl phosphate (TCP), phosphoric acid (hexichol -2- ethyl) oneself Ester；Fatty acid ester, such as the own ester of adipic acid two (2- ethyl), decanedioic acid two (2- ethyl) own ester；Epoxy compound species, such as epoxy Glyceride type, epoxy fatty acid monoester class, epoxy tetrahydrophthalic acid esters, epoxidised soybean oil, epoxystearic acid (2- second Base) own ester, epoxy soybean oleic acid 2- ethylhexyl, the own ester of 4,5- epoxy tetrahydrophthalic acid two (2- ethyl), Chinese littleleaf box acetyl Methyl ricinolcic acid, dihydric alcohol lipid, such as C_5~9Sour glycol ester, C_5~9Sour Triethylene Glycol；Class containing chlorine such as afforests stone Wax class, chloro fat acid esters；Polyesters, such as ethanedioic acid 1,2-PD system polyester, decanedioic acid 1,2-PD polyester；Petroleum sulphur Acid phenenyl ester, trimellitate, citrate, pentaerythrite and pentaerythritol fatty acid ester etc..Wherein, the preferred DBP, DOP of plasticizer, DIOP, DIDP, DINP, TCP, epoxidised soybean oil.Wherein, epoxidised soybean oil is that a kind of environment-friendly type plastic of function admirable increases Mould agent, epoxidation reaction preparation occurs for refined soybean oil and peroxide, in polymer product resistance to volatilization, it is not easy to migrate, Not easy to lose, this is to keeping product light, thermal stability and to prolong the service life be highly beneficial.Epoxidised soybean oil toxicity pole It is small, it is allowed for the packaging material of food and medicine by many countries, is that the unique of Food and Drug Adminstration of the US's approval can For the epoxy plasticiser of packaging material for food, therefore it is more highly preferred to.

In the preparation process of dynamic aggregation compositions, not to the dosage of dynamic aggregation compositions each component raw material It is particularly limited, those skilled in the art can be adjusted according to practical preparation situation and objective cross physical performance.

A kind of energy-absorbing method based on dynamic aggregation compositions provided by the present invention, when the dynamic aggregation object combines When being used for energy-absorbing without containing supermolecule hydrogen bond in object, dynamic aggregation compositions are preferably prepared into elastomer-forming, gel or foam Material carries out energy-absorbing；When containing supermolecule hydrogen bond for energy-absorbing in the dynamic aggregation compositions, polymer fibre can be The variforms such as dimension, film, profile, elastomer, foam, gel.Make when introducing supermolecule hydrogen bond in dynamic aggregation compositions With rear, by network structure dynamic covalent bond and supermolecule hydrogen bond combine, utilize the dynamic of supermolecule hydrogen bond and weaker Bond energy, there is flexible and strong elasticity transformation, plays effectively dispersion punching in the especially strain-responsive variation that generates the degree of cross linking Hit the effect of power；Furthermore supermolecule hydrogen bond has weaker bond energy, and when impacting sufficiently large, hydrogen bond can be can sacrifice key formal solution From and dissipation energy；Thus it is possible to which it is anti-to greatly improve the damping of dynamic aggregation compositions, damping, sound insulation, noise elimination, shock resistance The performances such as shield, to carry out the method for energy-absorbing in life, production, movement, leisure, amusement, military affairs, police with material of the invention There is more extensive energy-absorbing purposes in the fields such as business, security, medical care.For example, dynamic aggregation compositions material can be applied to Make damping shock absorber, for various motor vehicles, mechanical equipment, bridge, building vibration isolation, when being vibrated, The big energy that can dissipate plays damping, to effectively mitigate the vibration of vibration body；It prepares elastomer-forming, foam and coagulates Glue material, so as to be applied to airborne and air-drop protection, the shock resistance of collision prevention of vehicle, electronic apparatus article and precision machinery instrument With vibration damping protection etc., or athletic protective article, surge guard product, protector etc. is made for human body, animal body, article Deng carry out defense of resistance to impact in daily life, production and movement, or be used for the police protective materials of army etc.；It is prepared into explosion-proof Tent, blanket, wall, bulletproof glass squeegee, sandwich plate etc. carry out explosive-proof protector to article, reduce article or human body is including Suffered vibration and impact under the external forces such as the shock wave generated of exploding；Further, it is also possible to design with shape memory The energy-absorbing material of function is applied to specific occasion, prepares the energy-absorbing articles of personalized customization.With this dynamic aggregation compositions As energy-absorbing material, after endergonic process causes material internal cracked or is broken, its covalent and/or supermolecule dynamic is utilized Property, it can carry out recycled after selfreparing in situ, be also convenient for recycling and reprocess.

The energy-absorbing method of the present invention based on dynamic aggregation compositions is done below with reference to some specific embodiments It further describes.Specific embodiment is that present invention be described in more detail, non-limiting protection scope of the present invention.

Embodiment 1

A kind of dynamic aggregation compositions ordinary solid based on polyester is prepared for energy-absorbing.

It is acid chloride group by the converting carboxylate groups of acetylenedicarboxylic acid using thionyl chloride as chloride reagent.By 10 molar equivalents oneself two Acyl chlorides, 20 molar equivalent butine diacid chlorides, 27 molar equivalent hexylene glycols and 2 molar equivalent glycerol are anti-under the catalysis of triethylamine It answers, obtains the dynamic aggregation object component A that skeleton contains acetylene bond.

Above-mentioned copolymer and 5 mass parts of catalyst 20 obtained by 100 mass parts are sufficiently mixed, are placed in mold, after molding Obtain dynamic aggregation compositions product of the invention.Using product made of the dynamic aggregation compositions as shock proof portion Part carries out buffering energy-absorbing, when product is cracked, sprays the hot toluene solution (> 80 DEG C) containing zinc chloride, can carry out certainly It repairs and recycles and used as shock resistance component.

Embodiment 2

A kind of dynamic aggregation compositions ordinary solid based on polyethers is prepared for energy-absorbing.

By the iodo- 2,5- dimethyl ether of 13 molar equivalent 1,4- bis-, 10-ten polyethylene glycol of molar equivalent propinyl-propinyl and 2 Molar equivalent 1,3, (2- propargyl alcoholate) benzene of 5- tri- is blended, in two (triphenylphosphine) platinous chloride, cuprous iodide and diethylamine The lower reaction of catalysis, obtains dynamic aggregation compositions component A of the invention.

At room temperature, 5 mass parts urine is added into the aqueous solution of 250 mass parts ethylene maleic acid anhydride copolymers containing 0.5wt% Element, 0.5 mass parts ammonium chloride and 0.5 mass parts resorcinol, and pH value is modulated 3.5 by the way that sodium hydroxide or hydrochloric acid is added. Solution is stirred with the speed of 800rpm, and a small amount of n-heptanol defoaming is added.Solution into stirring is slowly added to 60 matter of toluene Part and 15 mass parts of protochloride manganese are measured, after emulsion-stabilizing, formalin are added, and keep obtaining mole of urea formadehyde It is frequently 1:1.8.Lotion is warming up to 55 DEG C with 1 DEG C of speed per minute, and keeps the temperature 4 hours.Later, it is kept stirring but stops Heating.After lotion is cooled to room temperature, washing obtains containing toluene and protochloride manganese ureaformaldehyde microcapsules.

100 content of component A are swollen in into DMF, and the micro- glue of ureaformaldehyde of 5 mass parts of mass parts of catalyst 18 and 10 is added Capsule removes solvent after being sufficiently blended, obtains dynamic aggregation compositions of the invention.The composition is used as Anti-impact shock-absorbing interlayer, When cracking in external force material, the generation or diffusion of crackle will lure the microcapsules rupture containing solvent into.Outflow Solvent infiltrates the polymer segment around crackle, and after protochloride manganese and catalyst action, can carry out selfreparing, material to crackle It can still continue to use and keep good energy-absorbing effect.

Embodiment 3

A kind of dynamic aggregation compositions ordinary solid based on unsaturated polyester (UP) is prepared for energy-absorbing, supermolecule therein Effect is based on side imidazoline ketone group, side amide groups and framework amide base.

At -78 DEG C, 1 molar equivalent δ-valerolactone is instilled into the tetrahydrofuran containing 1 molar equivalent lithium diisopropylamine Solution after stirring, is added the toluene solution of the 3- propargyl bromide containing 1.1 molar equivalents, is reacted at -40 DEG C. After reaction, by crude product at 140 DEG C short-path distillation, obtain internal ester monomer 3a.Under anhydrous condition, by 120 molar equivalent ε-oneself Lactone, 100 molar equivalent compound 3a are dissolved in toluene, in 1 molar equivalent initiator 2,2- dibutyl -2- tin -1,3- dioxy ring Heptane reacts under causing in 20 DEG C, obtains the polyester that side group contains alkynyl.

1 molar equivalent N- ethyl -2- chloroacetamide is dissolved in dimethylformamide (DMF), the nitrine of 2 molar equivalents is added Change sodium, converts azido for chlorine atom side group.Polyester, -2 nitrine acetamide of N- ethyl that side group is alkynyl are dissolved in tetrahydro furan It mutters, keeping the molar ratio of alkynyl and azido is that 2:1 obtains part in 35 DEG C of reactions under the catalysis of cuprous iodide and pyridine Side group is the polyester that alkynyl moiety side group is amide groups.100 mass parts resulting polymers are dissolved in toluene, are catalyzed with 5 mass parts Agent 22 is blended, and react 2 hours at 80 DEG C, except being to obtain dynamic aggregation compositions of the invention after solvent.In the present embodiment, With anti-impact protective device made of the composition material, when being cracked in material, crackle can be carried out at room temperature Selfreparing is heated to 80 DEG C, can shorten repair time, can be recycled after reparation.

Embodiment 4

A kind of dynamic aggregation compositions ionic liquid gel based on polyacrylate is prepared for energy-absorbing, it is therein super Molecular action is based on side thiocarbamate base.

Under the conditions of anhydrous and oxygen-free, by the isocyanates ethyl acrylate of ethyl mercaptan and equimolar equivalent under triethylamine catalysis It is reacted in methylene chloride, obtains the acrylate monomer 4a containing thio carbamate groups.By 2 molar equivalent acrylic acid and 1 molar equivalent 3,5- diine -1,8- ethohexadiol is urged bicyclic ethyl carbodiimide (DCC) and 4-dimethylaminopyridine (DMAP's) Change lower reaction, obtains compound 4b.

By 15 molar equivalent butyl methacrylates, 15 molar equivalent monomer 4a, 5 molar equivalent crosslinking agent 4c, 1 mole is worked as Photoinitiator 2- hydroxy-2-methyl -1- phenyl -1- acetone is measured in ionic liquid 1-butyl-3-methyl imidazolium hexafluorophosphate It is sufficiently mixed, and the quality of ionic liquid is the 50% of mixture total weight.In the UV lamp after illumination reaction 4 hours, moved The ionic liquid gel of state polymers compositions A.

By gained dynamic aggregation object ionic liquid gel, component B catalyst 16 and zinc chloride according to mass ratio 500:10:1 It is sufficiently mixed to get corresponding dynamic aggregation compositions ionic liquid gel is arrived.Using this ionic liquid gel as protection Pad, the impact for anti-external forces.

Embodiment 5

A kind of dynamic aggregation compositions foam based on polyurethane is prepared for energy-absorbing, supermolecular mechanism therein is based on Side thiocarbamate base, side carbamateyl, backbone amino formic acid ester group and skeleton urea groups.

Pure and mild third cysteine of a certain amount of 5- cyclo-octene -1,2- bis- is mixed, the ratio of both control molal quantity is about 1:2, using DCC and DMAP as catalyst, methylene chloride is solvent, obtains the Cyclooctene derivative monomer 5a of hydrogen bonds group.It will The ratio of the mixing of a certain amount of monomer 5a, 5- cyclo-octene -1,2- bis- pure and mild cyclo-octene, both control molal quantity is about 5:1:4, with Grubbs bis- generations catalyst is catalyst, and using methylene chloride as solvent, reaction obtains the polymer based on polycyclic octene.1 is rubbed You sufficiently react at equivalent Isosorbide-5-Nitrae-bis- (3- aminobenzene) diacetylene with 2 molar equivalent isophorone diisocyanate, obtain containing acetylene bond Diisocyanate 5b.

Under the conditions of anhydrous and oxygen-free, by 5 mass parts of catalyst 17,100 mass parts paraffin and under paraffin molten condition sufficiently It is blended.Surfactant ethylene maleic acid anhydride copolymer and n-octyl alcohol are added in ionic liquid, and keep mixture temperature About 80 DEG C.Solution with 900rpm revolving speed stirring in the case where, blend is poured into and stir to be blended liquid reach stable shape After state, reduce rapidly temperature.Stop stirring, filtering obtains the catalyst composites component B of paraffin cladding.

Above-mentioned side group is contained into the polycyclic octene, ethyl isocyanate, diisocyanate 5b of hydroxyl according to hydroxyl, isocyanic acid second Ester, diisocyanate 5b molar ratio are 10:8:1 mixing, and mixture is denoted as 100 mass parts.Add 50 mass parts montmorillonites, 0.2 mass parts organic silicone oil, the expandable polymer microballoon of 1.5 mass parts, 0.1 mass parts DBTDL, 0.1 mass parts triethylene The catalyst composites component B of diamines, 5 mass parts paraffin cladding, is uniformly mixed, and solidifies 30 minutes at room temperature.Exist later 80 DEG C of resolidifications 4 hours are to get arriving a kind of dynamic aggregation compositions foamed material containing carbamate groups.It can the bubble Foam material manufactures foam seat, is used for damping energy-absorbing.After slight crack occurs in foam, 6 hours can be kept the temperature in 50 DEG C, the stone at slight crack Catalyst is released after Wax particles dissolution, it can carries out reviewing one's lessons by oneself redoubling recycling to slight crack therein.

Embodiment 6

A kind of dynamic aggregation compositions flexible foam based on polyurethane is prepared for energy-absorbing, supermolecule crosslinking therein Based on side carbamateyl.

Under nitrogen protection, by 10 molar equivalent ethylene glycol monoallyl ethers (average molecular weight about 500) and 1 molar equivalent Potassium methoxide is blended, and the epoxy prapanol of 70 molar equivalents is slowly added dropwise at 95 DEG C, and obtaining end group is the alkene that hydroxyl has branched structure Hydrocarbon monomer 6a.It under nitrogen protection, is olefinic monomer 6a and and hydroxyl molar equivalent of the hydroxyl with branched structure by end group Ethyl isocyanate reacts in methylene chloride under the catalysis of DBTDL, obtains olefinic monomer 6b.

Olefinic monomer 6b is sufficiently blended with 3- sulfydryl -1,2-PD equimolar equivalent, 1wt% photoinitiator 2 is added, 2- dimethoxy -2- phenyl acetophenone, illumination 30 minutes under 300W ultraviolet lamp are obtained with cladodification pendant polyether group and cladodification side The glycol of base end amido-containing acid ester base.

X=direct key,

By the above-mentioned diol compound with hydrogen bond group of 30 molar equivalents, 20 molar equivalent polyether Glycols (molecular weight About 2000), 50 molar equivalent diethoxy butynediols, 98 molar equivalent toluene di-isocyanate(TDI)s are blended, and are calculated as 100 mass Part, add 1 mass of water-soluble organic silicone oil, 2 mass parts water, 0.2 mass parts DBTDL, 0.1 mass parts triethylenediamine The component B catalyst 17 (previous embodiment is shown in preparation) coated with 1 mass parts by paraffin, is uniformly mixed and quickly stirring extremely generates Bubble solidifies 15 minutes at room temperature, then solidifies at 60 DEG C 2 hours and steeps to get to dynamic aggregation compositions of the invention Foam product.The light softness of the product can be used as the filler of back cushion, headrest, pillow with damping, buffering function etc., be also suitable for The energy-absorbing application of human body, precision instrument, breakables protection etc., facilitates personal/fitting to use.

Embodiment 7

A kind of dynamic aggregation compositions ordinary solid based on unsaturated polyester (UP) is prepared for energy-absorbing, supermolecule therein Crosslinking is based on side carbamateyl and backbone amino formic acid ester group.

10,12-, 22 carbon diine diacid and polyethylene glycol diepoxide for example methyl ether are mixed according to molar ratio 1:1, A kind of polymer containing pendant hydroxyl group is prepared.By two hexamethylene of resulting polymers, ethyl isocyanate and 4,4- diisocyanate Methylmethane is sufficiently blended by pendant hydroxyl group, unitary isocyanates, binary isocyanates molar ratio 30:28:1, in the catalysis of DBTDL Under, obtain the dynamic aggregation object containing carbamate groups.

By 100 mass parts gained dynamic aggregation object, 5 parts by mass of cellulose are nanocrystalline and 3 mass parts of catalyst 20 are sufficiently mixed It closes to get corresponding dynamic aggregation compositions are arrived.This composition is suitble to require the application of high-intensitive energy-absorbing material, such as automobile Outer bumper preferably can protect automobile and interior driver, passenger in traffic accident shock；It can be also used for making such as vapour The components such as vehicle damping fin, noise reduction gear, soundproof plate, for damping, impact resistance, sound insulation in use process.

Embodiment 8

A kind of dynamic aggregation compositions ordinary solid based on vinyl alcohol-vinyl acetate is prepared for energy-absorbing, wherein Supermolecule crosslinking be based on side oxazolidine ketone group.

By a certain amount of vinyl alcohol-vinyl acetate random copolymer, (average molecular weight is about 10000, and alcoholysis degree is about 40%) it is dissolved in toluene with 5- chloromethyl -2- oxazolidone, Isosorbide-5-Nitrae-Dichloro-2-butine, using potassium carbonate as catalyst, with the tetrabutyl Ammonium bromide is consisting of phase-transferring agent, and keeping hydroxyl and 5- chloromethyl -2- oxazolidone, Isosorbide-5-Nitrae-Dichloro-2-butine molar ratio is about 5: 2:2 obtains the dynamic aggregation object component A containing side oxazolidine ketone group.

Dynamic aggregation object, 5 mass parts of catalyst 11 obtained by 100 mass parts are sufficiently mixed to get poly- to corresponding dynamic Polymer composition.The resulting dynamic aggregation compositions of the embodiment can be used as packaging material for bumper and absorbing shock, when material goes out When existing damaged, selfreparing can be carried out under room temperature.

Embodiment 9

A kind of dynamic aggregation compositions ionic liquid gel based on polyethers is prepared for energy-absorbing, supermolecule therein is made With based on side benzimidazolyl and framework amide base.

1H- benzimidazole -5- the acyl chlorides of the pure and mild equimolar equivalent of 1,4- pentadiine -3- is anti-under the catalysis of triethylamine It answers, obtains double alkyne monomer compound 9a.By the 6- heptynoic acid of equimolar equivalent and propargylamine in condensing agent 2- ethyoxyl -1- Acylation reaction is carried out in the presence of ethoxy carbonic acyl radical -1,2- dihydroquinoline, obtains the compound 9b that both ends are alkynyl.

Under anhydrous condition, by the ten poly- second two of double alkyne monomer compound 9a, double alkyne monomer compound 9b, double alkynes sealing end It is pure and mild to be dissolved in ionic liquid 1-butyl-3-methyl imidazolium bis trifluoromethyl sulfimide salt ([bmim] according to molar ratio 1:1:2 NTf2), the mass ratio for keeping the sum of material quality and ionic liquid is 1:1.And it is denoted as 100 mass parts.Add ionic liquid A kind of dynamic aggregation compositions ion can be obtained after room temperature is sufficiently mixed 4 hours in the catalyst 21 of weight 0.5% Liquid gel.The ionic liquid gel can be used as dropping the protecting against shock packaging protection of article.

Embodiment 10

A kind of dynamic aggregation compositions ordinary solid based on carbene propyl ether and polyacrylate is prepared for energy-absorbing, Supermolecular mechanism therein is based on secondary amino group, pyrazinyl and the imidazole radicals in side group.

10 molar equivalent monomer 10a are dissolved in tetrahydrofuran/methanol (3:7) mixed solution, in 2 molar equivalent catalyst Ring-opening polymerisation is carried out under 25 catalysis under ultraviolet light, after reaction 2 hours, concentration of reaction solution is added appropriate DMF and 2 mole Equivalent 4- piperidinecarboxylic acid, 1 molar equivalent 2- formic acid pyrazine, 2 molar equivalent imidazoles -4- acetic acid, 3 molar equivalents hendecanoic acid and 2 molar equivalents to cyclohexanecarboxylic acid, under the catalysis of DCC and DMAP, after complete reaction, obtain part side group and contain Hydrogen bond group skeleton contains the linear polymer of alkynyl.

By above-mentioned 100 mass parts of polymer, 20 mass parts calcium carbonate, 3 mass parts of catalyst 15,0.2 mass parts antioxidant 754 demould after abundant blending is placed on and shapes in mold to get dynamic aggregation compositions of the invention are arrived.The composition can As damping coatings, and there is good wearability.

Embodiment 11

A kind of dynamic aggregation compositions plasticizer swell gel based on polyvinyl chloride is prepared for energy-absorbing, it is therein super Molecular action is based on side urea groups.

Branching type polyvinyl chloride (average molecular weight about 50000) and 4- (2- pyrrolidinyl) benzenethiol are dissolved in hexamethylene and existed 60 DEG C are reacted 12 hours, and keeping the molar ratio of side group chlorine atom and 4- (2- pyrrolidinyl) benzenethiol is about 10:1, are contained The polyvinyl chloride of side secondary amino group.By in side group containing parahelium polyvinyl chloride and methyl isocyanate react in methylene chloride, protect The molar ratio for holding secondary amino group and methyl isocyanate is about 1:1, obtains side group containing the polyvinyl chloride for replacing urea groups.

It is anti-at 60 DEG C that branching type polyvinyl chloride (average molecular weight about 3000) and 4- iodobenzene -1- mercaptan are dissolved in hexamethylene It answers 12 hours, keeping the molar ratio of side group chlorine atom and 4- iodobenzene -1- mercaptan is about 4:1, is obtained poly- containing iodine substituted phenyl Vinyl chloride.By resulting polymers under the catalysis of two (triphenylphosphine) platinous chloride, cuprous iodide and diethylamine, with 1, the 9- last of the ten Heavenly stems two Alkyne reaction obtains the cross-linked polrvinyl chloride that skeleton contains alkynyl.

The resulting cross-linked polrvinyl chloride of 100 mass parts is swollen in into toluene, side group obtained by 100 mass parts is added and contains substituted urea The polyvinyl chloride of base, 70 mass parts epoxidized soybean oils, 50 mass parts tricresyl phosphates, 5 mass parts of mass parts of catalyst 19 and 1 Zinc chloride simultaneously removes solvent after mixing, obtains dynamic aggregation compositions plasticizer swell gel of the invention.With the material As packaging material, for providing excellent shock resistance.

Embodiment 12

A kind of dynamic aggregation compositions plasticizer swell gel based on crosslinked polyether and polyacrylonitrile is prepared to be used for Energy-absorbing, supermolecular mechanism therein are based on side carbamateyl and side urea groups.

By 13 molar equivalent paradiiodobenzenes, 10-ten polyethylene glycol of molar equivalent propinyl-propinyl and 2 molar equivalents 1, 3,5- tri- (2- propargyl alcoholate) benzene are blended, and react under the catalysis of two (triphenylphosphine) platinous chloride, cuprous iodide and diethylamine, Obtain the crosslinked polyethers that skeleton contains acetylene bond.

Cyanuric acid and the chloro- 1- hexene of 6- are kept into molar ratio 4:1, are dissolved in anhydrous dimethyl sulphoxide, is catalyzed in potassium carbonate Under be stirred to react at 80 DEG C 15 hours, obtain the olefinic monomer 12a of hydrogen bonds group.Toluene is added in compound 1a, it will be anti- Container is answered to be cooled to 5 DEG C, cyclopentadiene is added dropwise in low temperature, keeps compound 12a and cyclopentadiene molar ratio is 10:13. It is warming up to reflux temperature after being added dropwise to continue to be stirred to react, obtains the norbornene derivative 12b of hydrogen bonds group.It will be certain The norbornene derivative 12b and norbornene of amount hydrogen bonds group are under the catalysis of Grubbs bis- generations catalyst in methylene chloride The molar ratio of middle reaction, the norbornene derivative 12b and norbornene that keep hydrogen bonds group is 1:1, obtains side group and contains The line style polynorbornene of hydrogen bond group.

The resulting polynorbornene of 50 mass parts, 110 mass parts are uniformly mixed into naphthenic oil, 40 mass parts of carbon black, 10 matter Amount part carbon nanotube, 1 mass parts zinc chloride, 5 mass parts of catalyst 20 are sufficiently mixed, and swell in the resulting crosslinking of 100 mass parts Type polyethers, is placed in mold, and dynamic aggregation object plasticizer swell gel of the invention is obtained after molding.Made of this material Components are used for damping, impact resistance, sound insulation, while having good heating effect under near infrared light.

Embodiment 13

It prepares a kind of dynamic aggregation compositions foam based on polyester and polyethyleneimine and is used as energy-absorbing, oversubscription therein Son effect is based on Amino End Group formic acid ester group and end urea groups.

By the hydroxy-end capped polycaprolactone in both ends (average molecular weight is about 300) and 5- hexin acyl chlorides triethylamine catalysis Lower reaction obtains the polyester of two end alkynyl radicals sealing end.With 1 molar equivalent 2, the iodo- 4- methyl benzyl carbinol of 5- bis- is initiator, in octanoic acid The ring-opening reaction that 15 molar equivalent 6-caprolactones are carried out under the catalysis of stannous, it is the poly- of hydroxyl that obtain one end, which be diiodo- phenyl one end, Ester.It is two Terminal Acetylenes of polyester paradiiodobenzene and 9 molar equivalent that diiodo- phenyl one end is hydroxyl by the resulting one end of 10 molar equivalents The polyester and 1 molar equivalent, 1,2,4,5- tetraiodo-benzene of base sealing end are blended, in two (triphenylphosphine) platinous chloride, cuprous iodide and two Under the catalysis of ethamine, the dynamic aggregation object based on polyester is obtained.

By the branched polyethylene imine of resulting 100 mass parts of polyester and 50 mass parts (average molecular weight is about 20000) It is blended, is reacted with excessive ethyl isocyanate, obtain dynamic aggregation object component A of the invention.

Resulting 100 mass parts of dynamic aggregation object component A are swollen in into Isosorbide-5-Nitrae-dioxane solvent, 3 mass parts are added and urge Agent 11 is sufficiently blended.Blend is placed in mold and is freezed completely at -80 DEG C, aspiration pump is opened at -50 DEG C, remains dry Dry air pressure is dry in 20 DEG C of vacuum ovens less than 50 μ atm 24 hours, extracts whole solvents, obtains of the invention Dynamic aggregation compositions foamed material.Army and police's protective article, explosion-proof layer etc. is made with the material, is used for extraneous impact force such as The snubber of explosion wave is also used as the use of protectiveness carrier.

Embodiment 14

A kind of dynamic aggregation compositions ordinary solid based on polyether polyurethane is prepared for energy-absorbing, oversubscription therein Son effect is based on side carbamateyl, side amide groups, Amino End Group formic acid ester group, backbone amino formic acid ester group and framework amide Base.

By 1 molar equivalent ethylene glycol, 100 molar equivalent ethylene oxide, 50 molar equivalents (S)-(oxiranylmethyl) ammonia Base t-butyl formate, 50 molar equivalent 3- [(acetparaminosalol) phenoxy group] -1,2 epoxy prapane hybrid reaction preparation both ends are Pendant hydroxyl groups contain the polyethers of carbamate groups and amide groups.10 molar equivalent urea are instilled into 100 molar equivalent 4,4- bis- Isocyanates dicyclohexyl methyl hydride after abundant blending and stirring 24 hours, is cooled to 35 DEG C, adds 40 molar equivalent institutes in 70 DEG C Polyethers, 40 molar equivalents 2 obtained, 4- hexadiine -1,6- glycol, 10 molar equivalent ethanol amines and 1 molar equivalent DBTDL, sufficiently Reaction obtains crosslinked polyethers type polyurethane.

Under nitrogen protection, 5 molar equivalent pentaerythrites and 2 molar equivalent potassium methoxides are blended, are slowly added dropwise at 95 DEG C The epoxy prapanol of 300 molar equivalents, it is the polyethers of hydroxyl that obtaining, which has dissaving structure end group,.By gained polyethers with it is excessive different Ethyl cyanate reacts under the catalysis of DBTDL, and after complete reaction, it is carbamate that obtaining, which has dissaving structure end group, Polyethers.The hydroxy-end capped polyethylene glycol in both ends is reacted under the catalysis of DBTDL with excessive ethyl isocyanate, to fully reacting Afterwards, it is the polyethers of carbamate that obtaining, which has linear structure end group,.

Crosslinked polyethers type polyurethane obtained by 100 mass parts is swollen in into methylene chloride, the resulting modification of 100 mass parts is added The resulting polyethers with linear structure of hyperbranched polyether, 50 mass parts, 10 mass parts graphenes and 5 mass parts of catalyst 12, It is sufficiently blended after removing solvent and obtains dynamic aggregation compositions of the invention.With filler made from the composition, can be applied It is added on textile or is used in foams, have the function of bumper and absorbing shock, can also have hot sensing function.

Embodiment 15

A kind of dynamic aggregation compositions ordinary solid based on polyphenylacetylene and polyethylene is prepared for energy-absorbing, it is therein Supermolecular mechanism is based on triazoline diketone-ene adducts side group and side urea groups pyrimidine ketone group.

By bis- (2- ethylhexyl the oxygroup) -2,5- diiodo-benzenes of 9 molar equivalent 1,4- and 10 diynyl -2 molar equivalent 1,4-, 5- dioctyl oxygroup benzene reacts 20 hours under the catalysis of two (triphenylphosphine) platinous chloride, cuprous iodide and diethylamine in 70 DEG C Afterwards, the polyphenylacetylene that alkynyl sealing end has alkoxy side group is obtained.By 1,4- dichloroprene and excessive sodium azide two Reaction, converts azido for chlorine atom in methylformamide (DMF).By 10 molar equivalent resulting polymers and 9 molar equivalents Isosorbide-5-Nitrae-diazido butylene carry out nitrine alkynes click-reaction, obtain the linear polymerization containing alkynyl and alkenyl simultaneously on skeleton Object.

Low-density cladodification polyethylene (average molecular weight is about 20000) is dissolved by heating in dimethylbenzene, 100 moles is added and works as The initiator cumyl peroxide for being dissolved in dimethylbenzene, constant temperature is added after solution temperature rises to 130 DEG C in the maleic anhydride of amount Reaction obtained Research of Grafting Malaic Anhydride Onto Polyethylene after 1 to 3 hour.Under inert gas protection, UPy derivative 15a and gained are gathered Vinyl Graft maleic anhydride is dissolved in dimethylbenzene, and keeping the molar ratio of compound 15a and maleic anhydride side group is 1:1, and stirring is lower to be added Enter catalyst paratoluenesulfonic acid sodium salt, is stirred to react in 105 DEG C.By water in the dichloromethane solution of products therefrom and trifluoroacetic acid Solution, obtains the modified poly ethylene containing UPy side group hydrogen bond group.

By 2 molar equivalents and 1 molar equivalent 2,4-TDI is dissolved in hexamethylene with-two butanol of Isosorbide-5-Nitrae and reacts 24 hours at 80 DEG C, Obtain isocyanate-terminated prepolymer.Prepolymer obtained by 3 mass parts and 1 mass parts of catalyst 13 are dissolved in 30 mass parts Toluene, and add in the water of 30 mass parts, it is stirred 30 minutes with the speed of 1000rpm in 70 DEG C.By the chain extender second of 1 mass parts Glycol is slowly added in lotion, is maintained temperature revolving speed to continue stirring 2 hours, is obtained the catalyst using polyurethane as microcapsule shell Component B.

The resulting polymer of 100 mass parts, the resulting modified poly ethylene of 50 mass parts, 10 mass parts are contained into catalyst 13 Microcapsules, the odium stearate of 30 mass parts, the sodium bicarbonate of 8 mass parts, 0.2 mass parts vaseline oil and a certain amount of 4- Methyl-triazolidine -3,5- diketone and 4,4'- (di-2-ethylhexylphosphine oxide (4,1- phenylene)) bis- (3H- pyrazoles -3,5 (4H)-diketone) are altogether It is mixed, keep polymer double bond and 4- methyl-triazolidine -3,5- diketone, 4,4'- (di-2-ethylhexylphosphine oxide (4,1- phenylene)) bis- (3H- pyrroles Azoles -3,5 (4H)-diketone) molar ratio be 10:3:1, sufficiently after reaction, extrusion molding obtains corresponding foamed product, obtains this The dynamic aggregation compositions foam of invention.Using the dynamic aggregation compositions foamed product as damping part, it to be used for anti-impact Hit protection.

Embodiment 16

A kind of dynamic aggregation compositions ordinary solid based on crosslinking carbene propyl ether and polyethylene glycol is prepared for inhaling Can, supermolecular mechanism therein is based on end cytimidine base and end guanyl-.

Cytimidine is reacted under the catalysis of triethylamine with the polyethylene glycol that both ends are succinimidyl succinate base, is obtained It is the polyethylene glycol of cytimidine base to both ends.Guanine is existed with both ends for the polyethylene glycol of succinimidyl succinate base It is reacted under the catalysis of triethylamine, obtains the polyethylene glycol that both ends are guanyl-.

Dipropargyl ether is subjected to non-annularity diine metathesis reaction under the catalysis of catalyst 1, obtains line style carbene third Base ether.By the resulting carbene propyl ether of 100 mass parts, each 50 mass parts of resulting two kinds of polyethylene glycol, a certain amount of 1,6- oneself two Mercaptan and a certain amount of photoinitiator benzil dimethyl ketal (BDK) are blended in tetrahydrofuran, keep polymer in alkynyl with The molar ratio of two mercaptan and BDK are 600:30:1, and sufficiently after reaction, 2 mass parts of catalyst 12 are added, sufficiently miscible rear except molten Agent obtains dynamic aggregation compositions of the invention.Using the material as airborne and air-drop protective materials, for buffering anti-impact It hits.

Embodiment 17

Prepare it is a kind of based on the dynamic aggregation compositions foam of polyisobutene for energy-absorbing, supermolecular mechanism therein Based on Amino End Group formic acid esters-urea groups.

After 2, the 4- toluene di-isocyanate(TDI) of the amino-terminated polyisobutene in one end and equimolar equivalent is sufficiently reacted, Equimolar eq. ethanol is added, the reaction was continued under the catalysis of TDBDL, obtains the poly- isobutyl of modification that end hydrogen bond group is contained in one end Alkene.

Cycloalkyne monomer 17a is dissolved in toluene, carries out ring-opening polymerisation at room temperature under the catalysis of catalyst 1, keeps monomer Molar ratio with catalyst is about 10:1, obtains linear polymer 17b.

By 100 mass parts of linear polymer 17b, resulting 300 mass of modification polyisobutene containing end hydrogen bond group Part, 50 mass parts of polystyrene, 20 mass parts of polyvinyl acetate, two mercaptan of biphenyl -4,4'-, 2 mass parts and 0.2 matter of AIBN Amount part melts and is sufficiently mixed at 110-120 DEG C, and after being down to 60 DEG C, heat preservation 1 hour to temperature, 5 mass parts of catalyst 15 are added With the zinc chloride of 1 mass parts and be sufficiently mixed.Mold is filled this blend into, is placed in pressure reaction still, supersaturated dioxy is passed through To change carbon, is heated to 90 DEG C, pressure control is depressured after 7-14MPa, 4 hours with the speed of 1MPa per second, product cooled down rapidly, Dynamic aggregation compositions foamed product of the invention is obtained after demoulding.The foamed product can be used for damping, also act as simultaneously Light heat-insulating material.

Embodiment 18

A kind of dynamic aggregation compositions ordinary solid based on polycyclic octyne is prepared for energy-absorbing, supermolecule therein is made With based on side benzimidazolyl, diamides base naphthyridines end group and urea groups pyrimidone end group.

1 molar equivalent compound 18a and 1 molar equivalent benzimidazole -5- formic acid is anti-under the catalysis of DCC and DMAP It answers, obtains the monomer 18b containing benzimidazolyl.By 2 molar equivalent compound 18a and 1 molar equivalent Adipoyl Chloride in triethylamine Catalysis under react, obtain diine monomer 18c.100 molar equivalent monomer 18b and 3 molar equivalent monomer 18c are worked as at 10 moles It measures under the initiation of catalyst 24 in -78 DEG C of progress ring-opening polymerizations, obtains side group and contain thiocarbamate base skeleton containing The dynamic aggregation object network of alkynyl.

Using methylene chloride as solvent, it will be reacted by the polycaprolactone of end group of acid chloride group with ammonium hydroxide, obtain two end groups For the polycaprolactone of amide groups.With lead acetate, bis- diphenylphosphine -9, the 9- xanthphos of 4,5- and potassium carbonate for catalyst, By 10 molar equivalents 2, chloro- 1, the 8- naphthyridines of 7- bis- reacts in chloroform with 9 molar equivalent 2- ethyl hexanoyl ammonia, obtains one end and 2- The connected naphthyridines intermediate of ethyl hexanoyl amino.It is the poly- of amide groups by the resulting naphthyridines intermediate of 2 molar equivalents and two end groups Caprolactone reacts under the catalysis of lead acetate, bis- diphenylphosphine -9, the 9- xanthphos of 4,5- and potassium carbonate, obtains both ends and contains There is the polycaprolactone of 2,7- amide groups -1,8- naphthyridines end group.In anhydrous conditions, by 1 molar equivalent compound 18d and 1 mole Equivalent 2,6- diisopropyl phenylisocyanate are dissolved in tetrahydrofuran, react 16 hours at room temperature, obtain the UPy that one end is alkenyl Derivative 18e.By gained UPy derivative 18e respectively with the mercaptoethanol of equimolar equivalent BDK and ultraviolet light collective effect Lower reaction, converts hydroxyl for alkenyl.It is acyl by UPy derivative and 1 molar equivalent, two end group that 2 molar equivalent one end are hydroxyl The polycaprolactone of chloro reacts under the catalysis of triethylamine, obtains the polycaprolactone that UPy derivative base is contained at both ends.

2,7- amide groups -1,8- naphthyridines end group is contained at dynamic aggregation object network, 20 mass parts both ends obtained by 100 mass parts Polycaprolactone, the polycaprolactone of UPy derivative base is contained at 30 mass parts both ends, 5 mass parts of catalyst 17 are sufficiently mixed, obtain Dynamic aggregation compositions of the invention.With each based article made of this dynamic aggregation object, it is used for buffering energy-absorbing, due to its tool There is multiple transition temperature, also there is shape memory function.

Embodiment 19

Prepare a kind of dynamic aggregation compositions ordinary solid based on dimethyl silicone polymer and poly-β-hybroxybutyric acid For energy-absorbing, supermolecular mechanism therein is based on side imidazoline ketone group and skeleton urea groups.

By the high molecular weight poly-β-hybroxybutyric acid of 1 molar equivalent, (300000) PHB, average molecular weight are about dissolved in dichloromethane Alkane instills the mixed solution for containing 1000 molar equivalent p-methyl benzenesulfonic acid and 10000 molar equivalent 1,4-butanediol.It is anti-at room temperature It answers, with methanol extraction and rinses product, obtaining the low molecular weight poly-β-hybroxybutyric acid that both ends are hydroxyl, (average molecular weight is about 3000).By UPy derivative 18e that one end is alkenyl respectively with the thioacetic acid of equimolar equivalent in the common of BDK and ultraviolet light The lower reaction of effect, converts carboxyl for alkenyl.By the PHB and 2 molar equivalent carboxyls envelope that the resulting both ends of 1 molar equivalent are hydroxyl The UPy derivative at end reacts under the catalysis of DCC and DMAP, obtains the PHB that two end groups are UPy derivative.

Under nitrogen protection, amination dimethyl siloxane 19a is added in urea, keeps the molar ratio of urea and side amino It is down to room temperature, obtains the ketone group of imidazoline containing side and side ammonia after being to slowly warm up to 160 DEG C, heat preservation about 1 hour under stirring for 9:10 The modified dimethyl polysiloxane 19b of base.By bis- (3- aminobenzene) diacetylene of 1 molar equivalent 1,4- and 2 molar equivalent 1,5- naphthalenes Diisocyanate sufficiently reacts, and obtains a kind of diisocyanate containing unsaturated bond.

Under nitrogen protection, 100 mass parts molecular sieve SBA-1 and 2 mass parts of catalyst 11 are dispersed in toluene, at room temperature Stirring 6 hours is filtered and is eluted with n-hexane, obtains the molecular sieve for being loaded with catalyst after dry.

A certain amount of modified dimethyl polysiloxane 19b is blended with a certain amount of resulting unsaturated diisocyanate, is kept The molar ratio of side amino and isocyanate group is 1:1.02 in dimethyl silicone polymer, and it is sufficiently anti-in 60 DEG C to be calculated as 100 mass parts It answers.After complete reaction, adding the resulting both ends of 100 mass parts is UPy derivative PHB and the molecule for being loaded with catalyst Sieve removes solvent after being sufficiently blended, obtains dynamic aggregation compositions of the invention.

Using this elastomer as the sealing element of the component of electronic product, such as mobile phone, tablet computer, notebook, camera Deng charger interface, the plug of data line interface etc. etc., there is dust-proof, waterproof mesh again while protecting against shock damping 's.

Embodiment 20

Prepare a kind of dynamic aggregation compositions elastomer use based on poly- (2- oxazoline) and poly- (methyl) acrylate In energy-absorbing, supermolecular mechanism therein is based on side urea groups.

It is 1 molar equivalent hexynic acid of initiator as terminator using 1 molar equivalent p-methyl benzenesulfonic acid propynyl ester, carries out 10 moles The ring-opening polymerisation of equivalent 2- (3- ethylheptyl) -2- oxazoline obtains poly- (2- oxazoline) that both ends are blocked with alkynyl.13 are rubbed Poly- (the 2- oxazoline) and 2 molar equivalent 1,3,5- that equivalent paradiiodobenzene, the resulting both ends of 10 molar equivalents are blocked with alkynyl Three (2- propargyl alcoholate) benzene are blended, and react, obtain under the catalysis of two (triphenylphosphine) platinous chloride, cuprous iodide and diethylamine The crosslinking that skeleton contains acetylene bond gathers poly- (2- oxazoline).

Acrylic acid 2- amino-ethyl ester and 4- biphenyl isocyanates are reacted in methylene chloride, keep amino and different The molar ratio of cyanate is 1:1, obtains the acrylate monomer 20a containing urea groups.By isocyanates ethyl acrylate and n-propylamine It is reacted in methylene chloride, keeping the molar ratio of amino and isocyanates is 1:1, obtains the acrylate monomer containing urea groups 20b.Isocyanates ethyl acrylate and nafoxidine are reacted in methylene chloride, keep rubbing for isocyanates and amino You obtain the acrylate monomer 20c of the derivative containing urea bond than being 1:1.

1 molar equivalent photoinitiator 2- hydroxy-2-methyl -1- phenyl -1- acetone, 10 molar equivalent 20a, 30 moles are worked as Amount 20b, 10 molar equivalent 20c, 10 molar equivalent n-BMAs are sufficiently blended and polymerize under light illumination, obtain containing not Poly- (methyl) acrylate of the modification of ipsilateral urea groups.

Modified poly- (methyl) acrylate obtained by 50 mass parts is broken into particle, is had with suitable catalyst 12 and swelling The toluene solution that poly- (2- oxazoline) is crosslinked obtained by 100 mass parts is sufficiently blended, except obtaining dynamic aggregation of the invention after solvent Compositions.Using the material as athletes ' body protective device, such as knee-pad, neck guard material, body is impacted for external force Protection.

Embodiment 21

A kind of dynamic aggregation compositions oligomer swell gel based on polynorbornene and polyethers is prepared for energy-absorbing, Supermolecular mechanism therein is based on side carbamateyl and side amide groups.

It is catalyst with 1, carries out the ontology ring-opening polymerisation of cyclooctyne, obtains line style or cricoid polycyclic octyne.By gained Polycyclic octyne, both ends sulfydryl sealing end ten polyethylene glycol and photoinitiator b DK be blended, react, handed under ultraviolet lighting Join polycyclic octyne.

Using 1 molar equivalent ethyl alcohol as initiator, by 100 molar equivalent ethylene oxide, 50 molar equivalents (S)-(ethylene oxide Methyl) t-butyl carbamate, the preparation of 50 molar equivalent 3- [(acetparaminosalol) phenoxy group] -1,2 epoxy prapane hybrid reaction Side group contains the polyethers of carbamate groups and amide groups.

By polyethers obtained by 50 mass parts, 100 mass parts alkyl-blocked polyethylene glycol oligomer and 1 mass parts zinc chloride The resulting crosslinking polycyclic octyne of 100 mass parts is swollen in the catalyst 19 of 5 mass parts, obtains dynamic aggregation object group of the invention Close object.With the squeegee of compound glass made of this material and multi-layered board, for shellproof and explosion-proof etc..

Embodiment 22

A kind of dynamic aggregation compositions ordinary solid based on polyurethane and polysiloxanes is prepared for energy-absorbing, it is therein Supermolecular mechanism is based on side urea groups, side diamino triazine and side thymine base.

Using chloroplatinic acid as catalyst, by hydrogen containing siloxane and 2- vinyl -4,6- diamino-1,3,5-triazines and 1- (4- vinyl benzene methyl) thymidine reacts 3 hours at 90 DEG C in cyclohexanone, control hydrogen containing siloxane in silicon hydrogen with Compound 2- vinyl -4,6- diaminostilbene, 3,5- triazine, the molar ratio of 1- (4- vinyl benzene methyl) thymidine are 2:1: 1, obtain the polysiloxanes containing side hydrogen bond group.

With 1 molar equivalent 4,4'- azo bis- (4- cyano amylalcohols) is that initiator draws using 4- amylene-1-ol as chain-transferring agent 5 molar equivalent 20b and the polymerization of 10 molar equivalent n-butyl acrylates are sent out, the hydroxy-end capped polyacrylate in both ends is obtained.By 50 Polyacrylate, 50 molar equivalent Isosorbide-5-Nitraes-butynediols, 110 molar equivalent toluene di-isocyanate(TDI)s obtained by molar equivalent, 5 moles Equivalent 2- butine-Isosorbide-5-Nitrae-glycol is sufficiently blended with the hydrolysate of the etherate of epoxychloropropane, under the catalysis of DBTDL sufficiently Reaction, obtains dynamic aggregation object network.

100 mass parts dynamic aggregation object networks, 10 mass parts of catalyst 20,2 mass parts zinc chloride, 30 mass parts are contained The polysiloxanes of side hydrogen bond group and 15 mass parts polyvinylpyrrolidone microballoons are sufficiently blended, and it is poly- to obtain dynamic of the invention Polymer composition.Using the material as packaging material, for providing excellent shock resistance, while having certain moisture absorption anti- Damp function.

Embodiment 23

Prepare a kind of dynamic aggregation compositions ordinary solid based on poly- limonene carbonic ester and poly-β-hybroxybutyric acid For energy-absorbing, supermolecular mechanism therein is based on side pyrrolidone-base and side urea groups pyrimidine ketone group.

Under the conditions of 90 DEG C of anhydrous no air, limonene oxide and catalyst 23a are dissolved in toluene, keep limonene oxide Molar ratio with catalyst is 100:1, and 10bar carbon dioxide is passed through into reaction vessel, and reaction obtains poly- limonene carbonic ester 23b.A certain amount of resulting poly- limonene carbonic ester 23b is dissolved in chloroform, excessive 2 mercapto ethanol, the positive fourth of 3- mercaptopropionic acid is added Ester and azo-bis-isobutyl cyanide, keeping 2 mercapto ethanol, 3- mercaptopropionic acid N-butyl, the molar ratio of initiator is 3:7:3, at 60 DEG C Lower reaction obtains the poly- limonene carbonic ester that part side group is hydroxyl.It is the poly- limonene carbonic acid of hydroxyl by resulting part side group Ester, one end are the urea groups pyrimidone derivatives (see embodiment 19) of carboxyl, the blending of 10,12-, 22 carbon diine diacid, keep poly- Pendant hydroxyl group in limonene carbonic ester, the UPy derivative that one end is carboxyl, 22 carbon diine diacid of 10,12- molar ratio be 5: 4:1 obtains the cross-linking modified poly- limonene carbonic ester of the pyrimidone of urea groups containing side after fully reacting.

Poly-β-hybroxybutyric acid (average molecular weight about 20000) and maleic anhydride are dissolved in chlorobenzene, make the first of maleic anhydride Beginning mass-volume concentration is 3%.In 130 DEG C of addition benzoyl peroxides, make the initial concentration 0.2% of benzoyl peroxide, It is kept for thermotonus 6 hours, obtains poly-β-hybroxybutyric acid grafted maleic anhydride.Under inert gas protection, by poly- beta-hydroxy Butyrate grafted maleic anhydride and 4- hydroxy-2-pyrrolidinone are dissolved in dimethylbenzene, keep maleic anhydride side group and 4- hydroxyl -2- pyrrole The molar ratio of pyrrolidone is 1:2.1.It is added with stirring catalyst paratoluenesulfonic acid sodium salt, is stirred to react, is obtained containing side in 105 DEG C The modification poly-β-hybroxybutyric acid of pyrrolidone-base.

The resulting cross-linking modified poly- limonene carbonic ester of 100 mass parts is swollen in into dimethylbenzene, and 50 mass parts are added Modified poly-β-hybroxybutyric acid, the polyester tiny balloon of 50 mass parts, 5 mass parts of catalyst 18, remove solvent, obtain after being sufficiently mixed To dynamic aggregation compositions of the invention.The dynamic aggregation compositions primary raw material is renewable raw materials, is widely used as Non-returnable container material is used for damping protection.

The above description is only an embodiment of the present invention, is not intended to limit the scope of the invention, all to utilize this hair Equivalent structure or equivalent flow shift made by bright description is applied directly or indirectly in other relevant technology necks Domain is included within the scope of the present invention.

Claims

1. a kind of energy-absorbing method based on dynamic aggregation compositions, which is characterized in that provide a kind of dynamic aggregation compositions And energy-absorbing is carried out using it as energy-absorbing material, wherein the dynamic aggregation compositions include at least two component of A, B；Wherein, The dynamic aggregation compositions component A is the dynamic aggregation object comprising at least one cross-linked network, the dynamic aggregation Contain the unsaturated triple carbon-carbon bonds that alkynes cross metathesis metathesis reaction can occur in object；Wherein dynamic aggregation object combination Object component B is that the unsaturated triple carbon-carbon bonds generation alkynes cross metathesis in the catalysis dynamic aggregation compositions component A is multiple Catalyst, catalyst composites or the catalyst of decomposition reaction and the mixture of catalyst composites；Wherein, described to occur The unsaturated triple carbon-carbon bonds of alkynes cross metathesis metathesis reaction have the structure being shown below:

2. a kind of energy-absorbing method based on dynamic aggregation compositions according to claim 1, which is characterized in that wherein institute Also containing the hydrogen bond group that can form supermolecule hydrogen bond action in the dynamic aggregation object stated.

3. a kind of energy-absorbing method based on dynamic aggregation compositions according to claim 2, which is characterized in that wherein institute The dynamic aggregation compositions component A stated has one of network structure as described below:

Only one cross-linked network in the dynamic aggregation compositions component A, in the cross-linked network simultaneously containing dynamic altogether Valence crosslinking and supermolecule crosslinking, wherein the degree of cross linking of dynamic covalent cross-linking reaches its gel point or more, the crosslinking of supermolecule crosslinking Degree is in its gel point above and below；

Only one cross-linked network in the dynamic aggregation compositions component A, in the cross-linked network simultaneously containing dynamic altogether Valence crosslinking and supermolecule crosslinking, wherein the degree of cross linking of dynamic covalent cross-linking is in its gel point hereinafter, the degree of cross linking of supermolecule crosslinking More than its gel point；

Only one cross-linked network in the dynamic aggregation compositions component A, in the cross-linked network simultaneously containing dynamic altogether Valence crosslinking and supermolecule crosslinking, wherein the degree of cross linking of dynamic covalent cross-linking is in its gel point hereinafter, the degree of cross linking of supermolecule crosslinking In its gel point hereinafter, but the sum of the two degree of cross linking more than gel point；

Containing there are two networks in the dynamic aggregation compositions component A；Dynamic covalent cross-linking is contained only in 1st network, is handed over Connection degree is more than its gel point；Supermolecule crosslinking is contained only in 2nd network, the degree of cross linking is more than its gel point；

Containing there are two networks in the dynamic aggregation compositions component A；Covalent cross-linking containing dynamic and supermolecule in 1st network It is crosslinked, is crosslinked simultaneously containing dynamic covalent cross-linking and supermolecule in the cross-linked network, wherein the degree of cross linking of dynamic covalent cross-linking exists More than its gel point, the degree of cross linking of supermolecule crosslinking is in its gel point above and below；Supermolecule crosslinking is contained only in 2nd network, Its degree of cross linking is more than its gel point；

Contain a network in the dynamic aggregation compositions component A, wherein only covalent containing dynamic more than gel point Crosslinking, the supermolecule degree of cross linking are dispersed in dynamic covalent cross-linking network in its gel point supermolecule polymer below；

Contain a network in the dynamic aggregation compositions component A, is covalently handed over containing dynamic simultaneously in the cross-linked network Connection and supermolecule crosslinking, wherein the degree of cross linking of dynamic covalent cross-linking reaches its gel point or more, and the degree of cross linking of supermolecule crosslinking exists Its gel point above and below；The supermolecule degree of cross linking is dispersed in dynamic covalent cross-linking in its gel point supermolecule polymer below In network；

Contain a network in the dynamic aggregation compositions component A, wherein only covalent containing dynamic more than gel point Crosslinking, supermolecule polymer of the supermolecule degree of cross linking more than its gel point are dispersed in dynamic covalent cross-linking network with graininess In；

Contain a network in the dynamic aggregation compositions component A, is covalently handed over containing dynamic simultaneously in the cross-linked network Connection and supermolecule crosslinking, wherein the degree of cross linking of dynamic covalent cross-linking reaches its gel point or more, and the degree of cross linking of supermolecule crosslinking exists Its gel point above and below；Supermolecule polymer of the supermolecule degree of cross linking more than its gel point is dispersed in dynamic with graininess In state covalent cross-linking network.

4. a kind of energy-absorbing method based on dynamic aggregation compositions according to claim 2, which is characterized in that described At least one of hydrogen bond group is the hydrogen bond group containing hydrogen bond donor and hydrogen bond receptor simultaneously.

5. a kind of energy-absorbing method based on dynamic aggregation compositions according to claim 4, which is characterized in that wherein institute Contain while stating and contains at least one secondary amino group in the hydrogen bond group of hydrogen bond donor and hydrogen bond receptor.

6. a kind of energy-absorbing method based on dynamic aggregation compositions according to claim 2, which is characterized in that wherein institute At least a kind of hydrogen bond group is located at the side group or side chain or side group and side chain of the dynamic aggregation object in the hydrogen bond group stated.

7. a kind of energy-absorbing method based on dynamic aggregation compositions described in any claim in -6 according to claim 1, It is characterized in that, the dynamic aggregation compositions have following any character: ordinary solid, elastomer, gel, foam.

8. a kind of energy-absorbing method based on dynamic aggregation compositions described in any claim in -6 according to claim 1, It is characterized in that, the recipe ingredient for constituting the dynamic aggregation compositions further include it is following any or appoint it is several can additive Or usable object: other polymers, auxiliary agent, filler, sweller.

9. a kind of energy-absorbing method based on dynamic aggregation compositions according to claim 8, which is characterized in that wherein, The other polymers are selected from following any or appoint several: natural polymer, synthetic macromolecular compound；It is described Auxiliary agent be selected from it is following any or appoint it is several: catalyst, initiator, antioxidant, light stabilizer, heat stabilizer, dispersing agent, Emulsifier, fire retardant, toughener, coupling agent, solvent, lubricant, release agent, plasticizer, thickener, thixotropic agent, levelling agent, Toner, fluorescent whitening agent, delustering agent, antistatic agent, dehydrating agent, biocide mildewcide, foaming agent, blowing promotor, nucleating agent, rheology Agent；The filler is selected from following any or appoints several: inorganic non-metallic filler, metal packing, organic filler；Described is molten Swollen dose is selected from following any or appoints several: water, organic solvent, ionic liquid, oligomer, plasticizer.

10. a kind of energy-absorbing side based on dynamic aggregation compositions described in any claim in -6,9 according to claim 1 Method, which is characterized in that the energy-absorbing method is applied to defense of resistance to impact, damping, damping, buffering, explosion-proof, shellproof, sound insulation, disappears Sound.