CN110105907A - A kind of vehicle glass quick assembling one-component silane modified polyether seal glue and preparation method thereof - Google Patents

A kind of vehicle glass quick assembling one-component silane modified polyether seal glue and preparation method thereof Download PDF

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CN110105907A
CN110105907A CN201910313550.1A CN201910313550A CN110105907A CN 110105907 A CN110105907 A CN 110105907A CN 201910313550 A CN201910313550 A CN 201910313550A CN 110105907 A CN110105907 A CN 110105907A
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modified polyether
silane modified
quick assembling
component
vehicle glass
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CN110105907B (en
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杨海兵
李义博
郑品
石正金
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Ji Tai Chemical Inc Guangzhou
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Ji Tai Chemical Inc Guangzhou
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/02Non-macromolecular additives
    • C09J11/04Non-macromolecular additives inorganic
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/02Non-macromolecular additives
    • C09J11/06Non-macromolecular additives organic
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J171/00Adhesives based on polyethers obtained by reactions forming an ether link in the main chain; Adhesives based on derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/24Acids; Salts thereof
    • C08K3/26Carbonates; Bicarbonates
    • C08K2003/265Calcium, strontium or barium carbonate
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00Specific properties of additives
    • C08K2201/011Nanostructured additives
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/02Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
    • C08L2205/025Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend

Abstract

The invention discloses vehicle glass quick assembling one-component silane modified polyether seal glues, by weight, including following component part: silane modified polyether resin 30~60;Environment-friendlyplasticizer plasticizer 8~30;Filler 10~15;Supporting material 10~30;Thixotropic agent 0.1~1;Ultraviolet absorber 0.1~1;Light stabilizer 0.1~1;Antioxidant 0.2~2;Deicer 0.2~2;Crosslinking agent 1~10;Coupling agent 0.1~5;Catalyst 0.1~2.The invention also discloses preparation methods.While products obtained therefrom of the present invention guarantees sealant enough adhesive strength, promote the initial bond strenght of one-component silane modified polyether seal glue, fast, safety and environmental protection and the excellent performance of adhesive effect with adhering speed, the quick assembling technique suitable for the windshield of the vehicles such as passenger car, logistic car, fire fighting truck, skylight and side window glass.

Description

A kind of vehicle glass quick assembling one-component silane modified polyether seal glue and its system Preparation Method
Technical field
The invention belongs to Automobile sealant fields, and in particular to a kind of vehicle glass quick assembling one-component silane changes Property polyether seal glue and preparation method thereof.
Background technique
With the raising of automobile manufacturing process level, the use of new material new technology and client to vehicle economy, relax The raising that adaptive requires, the new varieties of sealant, new process on automobile using more and more extensive, and shockproof, heat-insulated, anti- The work that corruption, antirust, leakproof, reduction noise, mitigation self weight, the comfort for improving automobile and safety etc. have this special With.In order to improve the safety of automobile, the safety of occupant is ensured, because of vehicle window glass when preventing from bringing to a halt or colliding in high speed is advanced Glass assembly loosely makes passenger come to harm, and is combined into using the glass for vehicle window that the direct technique for sticking of glass for vehicle window is with vehicle body One entirety has greatly reinforced the rigidity of car body, and glass and vehicle body binding force increase, and improve the sealing effect of vehicle window.
The bonding of vehicle factor glass for vehicle window also mainly continues to use the assembly technology of traditional one-component polyurethane sealant at present, behaviour It is simple and convenient to make technique, excellent in mechanical performance.But that there is also curing rates is slow for traditional one-component glass assembly glue, it is initial to be bonded The problem of intensity settling time length, to influence the construction rhythm of vehicle factor.Therefore, exploitation a new generation is environmentally friendly, quick-setting Glass assembly glue and gradually substitution monocomponent polyurethane glue are development trends from now on.
And in order to realize the quick assembling in vehicle factor construction site, the curing rate for promoting product at this stage mainly uses Two-component technical solution, different from the solidification mode of one-component from outward appearance to inner essence, two-component sealant may be implemented in table while solid Change, therefore there is very big advantage on rapid curing, but for comparing the operation of one-component, two component is applied in vehicle factor The constructing operation at work scene is complicated, very high for the skill requirement of operative employee, will lead to behaviour if it cannot reach skill requirement Many process times will be slatterned by making the bad usually pre-processing of convenience.
The initial bond strenght (4h adhesive strength) of the silane modified polyether seal glue of the one-component further developed exists It is found in actual application or not high enough.
Summary of the invention
The invention solves technological difficulties be to promote one-component silicon while ensure that sealant enough adhesive strength The initial bond strenght (4h adhesive strength) of alkane modified polyether seal glue.
One of the objects of the present invention is to provide a kind of vehicle glass quick assembling one-component silane modified polyethers to seal Glue.
The second object of the present invention is to provide the vehicle glass quick assembling one-component silane modified polyether sealing The preparation method of glue.
One of in order to achieve the object of the present invention, used technical solution is:
A kind of vehicle glass quick assembling one-component silane modified polyether seal glue, according to parts by weight, including it is as follows Component part:
Wherein, the silane modified polyether resin is that methyl dimethoxysilane modified polyether and trimethoxy silane are modified The mixture of polyethers, wherein the viscosity of methyl dimethoxysilane modified polyether is 10000mPa.s~50000mPa.s;Front three The viscosity of oxysilane modified polyether is 10000mPa.s~30000mPa.s;The compounding ratio of the silane modified polyether resin It is 2~4:1 that example (weight fraction ratio), which is methyl dimethoxysilane modified polyether/trimethoxy silane modified polyether,.
In a preferred embodiment of the invention, the methyl dimethoxysilane modified polyether be SAX260, Any one or more in S303H, SAX 350, SAX400 and SAX750.
In a preferred embodiment of the invention, the trimethoxy silane modified polyether is in SAX530, SAX580 Any one or more.
In a preferred embodiment of the invention, the environment-friendlyplasticizer plasticizer is polypropylene glycol 2000, polypropylene glycol 3000, hexamethylene 1, it is any one in 2- dioctyl phthalate diisononyl esters, diisononyl phthalate and phenyl alkylsulf Kind is a variety of.
In a preferred embodiment of the invention, the filler be active nano-calcium carbonate, silicon powder, kaolin and Any one or more in activated Calcium carbonate.
In a preferred embodiment of the invention, it is 120m that the supporting material, which is specific surface,2/ g~140m2The powder of/g Any one of shape carbon black or gas-phase silica.
In a preferred embodiment of the invention, the thixotropic agent is low-temperature activation polyamide wax, gas phase dioxy Any one or more in SiClx.
In a preferred embodiment of the invention, the ultraviolet absorber is 2- (2 '-hydroxyls -3 ', 5 '-two tertiary pentyls Phenyl) benzotriazole (Tinuvin 328), 2- (2 '-hydroxyls -3 '-tert-butyl -5 '-aminomethyl phenyl) -5- chlorinated benzotriazole (Tinuvin 326), 2- (2 '-hydroxyls -5 '-aminomethyl phenyl)-benzotriazole (UV-P), 2- (2 '-hydroxyls -3 ', 5 '-two tertiary fourths Base phenyl) the chloro- benzotriazole of -5- (Tinuvin 327), 2- (2 '-hydroxyls -5 '-tert-butyl-phenyl)-benzotriazole (Tinuvin 5411), any one in 2-2 '-methylene-(6- (2H- benzotriazole) -4- t-octyl) phenol (Tinuvin 5431) or It is a variety of.
In a preferred embodiment of the invention, the light stabilizer is poly- (1- ethoxy -2,2,6,6- tetramethyls - 4- hydroxy piperidine) succinate (Tinuvin 622), bis- (2,2,6,6- tetramethyl -4- piperidyl) sebacic acid ester (Tinuvin 770), any one or more in the double 1- octyloxy -2,2,6,6- tetramethyl piperidine alcohol esters (Tinuvin 523) of sebacic acid.
In a preferred embodiment of the invention, the antioxidant is β (3,5- di-tert-butyl-hydroxy phenyl) propionic acid Pentaerythritol ester (Irganox 1010), 3,5- di-tert-butyl-hydroxy phenyl propionic acid octadecanol ester (Irganox 1076), N, N- be bis--[β (3,5- di-tert-butyl-hydroxy phenyl) propionyl] -1,6- hexamethylene diamine (Irganox 1098), triethylene glycol ether - Two (3- tertiary butyl-4-hydroxy -5- aminomethyl phenyl) propionic esters (Irganox 245), (3,5- di-t-butyl -4- hydroxyl of 1,3,5- tri- Base benzyl) 1,3,5- triazine -2,4,6- (1H, 3H, 5H)-triketone (Irganox 3114), three (2,4- di-tert-butyl-phenyls) Asia Phosphate (Irgafos 168), bis- (3,5- di-tert-butyl-phenyl) pentaerythritol diphosphites (Irgafos 126), 3,3- Any one or more in propane thioic acid laurel alcohol ester (DLTDP).
In a preferred embodiment of the invention, the deicer is vinyltrimethoxysilane, three second of vinyl Any one or more in oxysilane and vinyl dimethoxysilane;The crosslinking agent is ethyl orthosilicate.
In a preferred embodiment of the invention, the coupling agent is gamma-aminopropyl-triethoxy-silane, γ-ammonia third Base trimethoxy silane, N- β-(aminoethyl)-γ-aminopropyltrimethoxysilane and N- β-(aminoethyl)-γ-aminopropyl first Base dimethoxysilane,γ mercaptopropyitrimethoxy silane, γ-sulfydryl Propyl-triethoxysilicane, γ-glycidyl ether oxygen propyl trimethoxy silicane, γ-glycidyl ether oxygen propyl triethoxy Any one or more in silane, γ-methacryloxypropyl trimethoxy silane.
In a preferred embodiment of the invention, the catalyst be more alcoxyl fundamental mode titanate esters, tin dilaurate two just In tin octylate, bis- (acetopyruvic acid) dibutyl tins and bis- (beta-diketo-ester) complexs of dialkoxy titanium any one or it is more Kind.
In order to achieve the object of the present invention two, used technical solution is:
A kind of preparation method of vehicle glass quick assembling one-component silane modified polyether seal glue, including walk as follows It is rapid:
(1) nanofiller and reinforced filling is 2.5~3.5 hours dry under the conditions of 110 DEG C~130 DEG C, it is spare;
(2) silane modified polyether resin, environment-friendlyplasticizer plasticizer, thixotropic agent, filler, supporting material are sequentially added in planet kettle And the deicer that mass fraction is 15%~25%, high speed dispersion 30min~40min;Then vacuum degree be -0.09MPa~- 20min~30min is stirred under conditions of 0.1MPa;
(3) sequentially adding ultraviolet absorber, light stabilizer, antioxidant, ethyl orthosilicate, coupling agent, mass fraction is 75%~85% deicer and catalyst are simultaneously uniformly mixed, and are stirred under conditions of vacuum degree is -0.09MPa~-0.1MPa 20min~40min is mixed, is discharged up to product.
The beneficial effects of the present invention are:
The present invention changes while guarantee sealant enough adhesive strengths by using the active two kinds of silane of differential responses The compounding and crosslinking curing system of property polyether resin, improve the initial bond strenght of one-component silane modified polyether seal glue (4h adhesive strength), to realize the function of rapid link positioning;Field operation time has been saved, the operation stream at scene is simplified Journey.The production assembly efficiency of vehicle factor can be significantly improved.
Detailed description of the invention
Fig. 1 is that existing two-component packs schematic diagram 1.
Fig. 2 is that existing two-component packs schematic diagram 2.
Specific embodiment
Technical key point of the present invention is further illustrated below by embodiment:
This patent is urged using the synergistic effect of the active resin compound system of differential responses, ethyl orthosilicate and catalyst Changing to be formed, there is the cross-linking system of interpenetrating networks to improve initial bonding to effectively improve the curing performance of this product Intensity, to realize the function of rapid link positioning;The simple production process of this patent product is easily accomplished scale production, It can be widely applied and significantly improve the production assembly efficiency of vehicle factor.
Compounding principle of the invention is:
The end group of trimethoxy silane modified polyether has very high reactivity, in cooperateing with for crosslinking agent and catalyst It under effect, can be reacted with the moisture in environment rapidly, and form preliminary cross-linked structure, so that assigning product initial stage must The adhesive strength wanted;In comparison, the terminal reactive of dimethoxysilane modified polyether is lower, and reaction speed lags behind front three Oxysilane modified polyether, with the continuity of time, dimethoxysilane modified polyether resin continues to participate in cross-linking reaction, thus The structure of interpenetrating networks is formed, the final adhesive strength of product is further promoted, and it is highly beneficial to ensure that the product has Mechanical property.At the same time, test of many times the result shows that, the compound proportion of two kinds of silane modified polyether resins is between 2~4:1 Between effect it is most prominent, when the accounting of trimethoxy silane modified polyether is higher, the crosslink density of obtained product is high, just Beginning adhesive strength can satisfy quick-setting requirement, but product embrittlement simultaneously, and elongation rate of tensile failure is not able to satisfy wanting for standard It asks;When the accounting of trimethoxy silane modified polyether is lower, the initial bond strength of acquired product is unable to satisfy quickly solid The requirement of change.
Performance test
In the present invention, performance test with the following method:
The tensile strength of sealant and the test method of elongation at break: GB/T 528-2009 vulcanized rubber or heat are referred to The measuring method (II type dumbbell plate) of plastic rubber tensile stress-strain performance;
The test method of the initial bond strenght of sealant: with reference to GB/T 7124-2008 adhesive tensile shear strength It measures (rigid material is to rigid material).
Embodiment 1
The weight part ratio of the component of embodiment 1 such as the following table 1:
Table 1
Preparation method
(1) nanometer calcium carbonate and height is 3 hours drier under the conditions of 120 DEG C than table carbon black, it is spare;
(2) S303H, SAX530, phenyl alkylsulf, polyamide wax, nanometer calcium carbonate, high ratio are sequentially added in planet kettle The vinyltrimethoxysilane of table carbon black and mass fraction 20%, high speed dispersion 30min~40min;Then vacuum degree be- 20min~30min is stirred under conditions of 0.09MPa~-0.1MPa;
(3) sequentially add Tinuvin 326, Tinuvin 770, Irganox 1010, ethyl orthosilicate,The vinyltrimethoxysilane of mass fraction 80% and bis- (acetopyruvic acid) dibutyl tins are simultaneously It is uniformly mixed, 20min~40min is stirred under conditions of vacuum degree is -0.09MPa~-0.1MPa, is discharged to obtain the final product.
Embodiment 2
The weight part ratio of the component of embodiment 2 such as the following table 2:
Table 2
Preparation method
(1) nanometer calcium carbonate and height is 3 hours drier under the conditions of 120 DEG C than table carbon black, it is spare;
(2) SAX400, SAX580, phenyl alkylsulf, polyamide wax, nanometer calcium carbonate, height are sequentially added in planet kettle Than table carbon black and the vinyltrimethoxysilane of mass fraction 20%, high speed dispersion 30min~40min;Then in vacuum degree To stir 20min~30min under conditions of -0.09MPa~-0.1MPa;
(3) Tinuvin 326, Tinuvin 770, Irganox 1010, ethyl orthosilicate, N- β-(ammonia second are sequentially added Base)-γ-aminopropyltriethoxy dimethoxysilane, γ-glycidyl ether oxygen propyl trimethoxy silicane, mass fraction 80% Vinyltrimethoxysilane and bis- (acetopyruvic acid) dibutyl tins are simultaneously uniformly mixed, vacuum degree be -0.09MPa~- It stirs 20min~40min under conditions of 0.1MPa, discharges to obtain the final product.
Embodiment 3
The weight part ratio of the component of embodiment 3 such as the following table 3:
Table 3
Preparation method
(1) nanometer calcium carbonate and height is 3 hours drier under the conditions of 120 DEG C than table carbon black, it is spare;
(2) SAX400, SAX580, hexamethylene 1 are sequentially added in planet kettle, 2- dioctyl phthalate dinonyl, is received polyamide wax The vinyltrimethoxysilane of rice calcium carbonate, Gao Bibiao carbon black and mass fraction 20%, high speed dispersion 30min~40min;So 20min~30min is stirred under conditions of vacuum degree is -0.09MPa~-0.1MPa afterwards;
(3) sequentially add Tinuvin 326, Tinuvin 770, Irganox 1010, ethyl orthosilicate,The vinyltrimethoxysilane of mass fraction 80% and bis- (acetopyruvic acid) dibutyl tins simultaneously mix Uniformly, 20min~40min is stirred under conditions of vacuum degree is -0.09MPa~-0.1MPa, is discharged to obtain the final product.
Embodiment 4
The weight part ratio of the component of embodiment 4 such as the following table 4:
Table 4
Preparation method
(1) nanometer calcium carbonate and height is 3 hours drier under the conditions of 120 DEG C than table carbon black, it is spare;
(2) SAX350, SAX580, diisononyl phthalate, polyamide wax, nano-calcium carbonate are sequentially added in planet kettle The vinyltrimethoxysilane of calcium, Gao Bibiao carbon black and mass fraction 20%, high speed dispersion 30min~40min;Then true Reciprocal of duty cycle stirs 20min~30min under conditions of being -0.09MPa~-0.1MPa;
(3) Tinuvin 326, Tinuvin 770, Irganox 1010, ethyl orthosilicate, γ-aminopropyl are sequentially added Trimethoxy silane, γ-glycidyl ether oxygen propyl trimethoxy silicane, mass fraction 80% vinyltrimethoxysilane And bis- (acetopyruvic acid) dibutyl tins and be uniformly mixed, it is stirred under conditions of vacuum degree is -0.09MPa~-0.1MPa 20min~40min discharges to obtain the final product.
Comparative example 1
The weight ratio of the component of comparative example 1 such as the following table 5:
Table 5
Preparation method
(1) nanometer calcium carbonate and height is 3 hours drier under the conditions of 120 DEG C than table carbon black, it is spare;
(2) SAX750, diisononyl phthalate, polyamide wax, nanometer calcium carbonate, high ratio are sequentially added in planet kettle The vinyltrimethoxysilane of table carbon black and mass fraction 20%, high speed dispersion 30min~40min;Then vacuum degree be- 20min~30min is stirred under conditions of 0.09MPa~-0.1MPa;
(3) Tinuvin 326, Tinuvin 770, Irganox 1010, ethyl orthosilicate, γ-aminopropyl are sequentially added Trimethoxy silane, γ-glycidyl ether oxygen propyl trimethoxy silicane, mass fraction 80% vinyltrimethoxysilane And bis- (acetopyruvic acid) dibutyl tins and be uniformly mixed, it is stirred under conditions of vacuum degree is -0.09MPa~-0.1MPa 20min~40min discharges to obtain the final product.
Comparative example 2
The weight ratio of the component of comparative example 2 such as the following table 6:
Table 6
Preparation method
(1) nanometer calcium carbonate and height is 3 hours drier under the conditions of 120 DEG C than table carbon black, it is spare;
(2) SAX400, diisononyl phthalate, polyamide wax, nanometer calcium carbonate, high ratio are sequentially added in planet kettle The vinyltrimethoxysilane of table carbon black and mass fraction 20%, high speed dispersion 30min~40min;Then vacuum degree be- 20min~30min is stirred under conditions of 0.09MPa~-0.1MPa;
(3) sequentially add Tinuvin 326, Tinuvin 770, Irganox 1010, γ-aminopropyl trimethoxy silicon Alkane, γ-glycidyl ether oxygen propyl trimethoxy silicane, the vinyltrimethoxysilane of mass fraction 80% and bis- (second Acyl pyruvic acid) dibutyl tin and be uniformly mixed, under conditions of vacuum degree is -0.09MPa~-0.1MPa stirring 20min~ 40min discharges to obtain the final product.
Comparative example 3
The weight part ratio of the component of comparative example 3 such as the following table 7:
Table 7
Preparation method
(1) nanometer calcium carbonate and height is 3 hours drier under the conditions of 120 DEG C than table carbon black, it is spare;
(2) SAX350, diisononyl phthalate, polyamide wax, nanometer calcium carbonate, high ratio are sequentially added in planet kettle The vinyltrimethoxysilane of table carbon black and mass fraction 20%, high speed dispersion 30min~40min;Then vacuum degree be- 20min~30min is stirred under conditions of 0.09MPa~-0.1MPa;
(3) Tinuvin 326, Tinuvin 770, Irganox 1010, γ-aminopropyl trimethoxy silicon are sequentially added Alkane, γ-glycidyl ether oxygen propyl trimethoxy silicane, the vinyltrimethoxysilane of mass fraction 80% and bis- (second Acyl pyruvic acid) dibutyl tin and be uniformly mixed, under conditions of vacuum degree is -0.09MPa~-0.1MPa stirring 20min~ 40min discharges to obtain the final product.
Comparative example 4
The weight part ratio of the component of comparative example 4 such as the following table 8:
Table 8
Preparation method
(1) nanometer calcium carbonate and height is 3 hours drier under the conditions of 120 DEG C than table carbon black, it is spare;
(2) SAX580, SAX350, diisononyl phthalate, polyamide wax, nano-calcium carbonate are sequentially added in planet kettle The vinyltrimethoxysilane of calcium, Gao Bibiao carbon black and mass fraction 20%, high speed dispersion 30min~40min;Then true Reciprocal of duty cycle stirs 20min~30min under conditions of being -0.09MPa~-0.1MPa;
(3) Tinuvin 326, Tinuvin 770, Irganox 1010, γ-aminopropyl trimethoxy silicon are sequentially added Alkane, γ-glycidyl ether oxygen propyl trimethoxy silicane, the vinyltrimethoxysilane of mass fraction 80% and bis- (second Acyl pyruvic acid) dibutyl tin and be uniformly mixed, under conditions of vacuum degree is -0.09MPa~-0.1MPa stirring 20min~ 40min discharges to obtain the final product.
Comparative example 5
The weight part ratio of the component of comparative example 5 such as the following table 9:
Table 9
Preparation method
(1) nanometer calcium carbonate and height is 3 hours drier under the conditions of 120 DEG C than table carbon black, it is spare;
(2) SAX580, SAX400, diisononyl phthalate, polyamide wax, nano-calcium carbonate are sequentially added in planet kettle The vinyltrimethoxysilane of calcium, Gao Bibiao carbon black and mass fraction 20%, high speed dispersion 30min~40min;Then true Reciprocal of duty cycle stirs 20min~30min under conditions of being -0.09MPa~-0.1MPa;
(3) Tinuvin 326, Tinuvin 770, Irganox 1010, γ-aminopropyl trimethoxy silicon are sequentially added Alkane, γ-glycidyl ether oxygen propyl trimethoxy silicane, the vinyltrimethoxysilane of mass fraction 80% and bis- (second Acyl pyruvic acid) dibutyl tin and be uniformly mixed, under conditions of vacuum degree is -0.09MPa~-0.1MPa stirring 20min~ 40min discharges to obtain the final product.
Single component silane modified polyether seal glue prepared by above-described embodiment and comparative example is subjected to Mechanics Performance Testing, it is main Wanting test index includes tensile strength, elongation, the 4h shear strength (initial bond strenght) of sealant.As a result such as 10 institute of table Show.
Each embodiment silane modified polyether seal glue mechanical experimental results of table 10.
Table 10
With comparison of the existing two-component materials in construction:
And existing two-component construction packaging such as Fig. 1,2, two-component sealant is divided into A, B component, wherein general component A is Host agent, B component are catalyst system.It is squeezed out by the equipment of Fig. 2, then carries out AB mixing by squeezing out sharp mouth, then be glued base Material surface.Different from the curing mode of one pack system from outward appearance to inner essence, two-component solidifies simultaneously to be inside and outside, thus needs to guarantee sharp mouth In time for mixing of A/B need very short, and the glue for mixing metacone face in the mouth must be also finished at once, otherwise be needed to frequently replace Sharp mouth, compares common one pack system point mouth, and the cost of the Jiao Zui is higher.
Two-component is because of its complicated situ configuration technique, although actually it is advantageous on curing time, by The time and cost for causing it finally to spend in complicated complex process are more.
Obviously, the above embodiment of the present invention be only to clearly illustrate example of the present invention, and not be pair The restriction of embodiments of the present invention.For those of ordinary skill in the art, may be used also on the basis of the above description To make other variations or changes in different ways.There is no necessity and possibility to exhaust all the enbodiments.It is all this Made any modifications, equivalent replacements, and improvements etc., should be included in the claims in the present invention within the spirit and principle of invention Protection scope within.

Claims (10)

1. a kind of vehicle glass quick assembling one-component silane modified polyether seal glue, which is characterized in that by weight, packet Include following component part:
Wherein, the silane modified polyether resin is methyl dimethoxysilane modified polyether and trimethoxy silane modified polyether Mixture, wherein the viscosity of methyl dimethoxysilane modified polyether be 10000mPa.s~50000mPa.s;Trimethoxy The viscosity of silane modified polyether is 10000mPa.s~30000mPa.s;The compound proportion of the silane modified polyether resin, It calculates by ratio of weight and the number of copies, be methyl dimethoxysilane modified polyether/trimethoxy silane modified polyether is 2~4:1.
2. a kind of vehicle glass quick assembling one-component silane modified polyether seal glue as described in claim 1, feature It is, the methyl dimethoxysilane modified polyether is appointing in SAX260, S303H, SAX350, SAX400 and SAX750 It anticipates one or more.
3. a kind of vehicle glass quick assembling one-component silane modified polyether seal glue as described in claim 1, feature It is, the trimethoxy silane modified polyether is any one or more in SAX530, SAX580.
4. a kind of vehicle glass quick assembling one-component silane modified polyether seal glue as described in claim 1, feature Be, the environment-friendlyplasticizer plasticizer be polypropylene glycol 2000, polypropylene glycol 3000, hexamethylene 1,2- dioctyl phthalate diisononyl esters, Any one or more in diisononyl phthalate and phenyl alkylsulf, the filler are active nano carbonic acid Any one or more in calcium, silicon powder, kaolin and activated Calcium carbonate, the supporting material is that specific surface is 120m2/ G~140m2Any one of the powdered carbon black of/g or gas-phase silica.
5. a kind of vehicle glass quick assembling one-component silane modified polyether seal glue as described in claim 1, feature It is, the thixotropic agent is low-temperature activation polyamide wax, any one or more in fumed silica.
6. a kind of vehicle glass quick assembling one-component silane modified polyether seal glue as described in claim 1, feature It is, the ultraviolet absorber is 2- (2 '-hydroxyls -3 ', 5 '-di-tert-pentyl-phenyls) benzotriazole, 2- (2 '-hydroxyls -3 '-uncle Butyl -5 '-aminomethyl phenyl) -5- chlorinated benzotriazole, 2- (2 '-hydroxyls -5 '-aminomethyl phenyl)-benzotriazole, 2- (2 '-hydroxyls - 3 ', 5 '-di-tert-butyl-phenyls) the chloro- benzotriazole of -5-, 2- (2 '-hydroxyls -5 '-tert-butyl-phenyl)-benzotriazole, the Asia 2-2 ' - One of methyl-(6- (2H- benzotriazole) -4- t-octyl) phenol and its more than;The light stabilizer is poly- (1- hydroxyl second Base -2,2,6,6- tetramethyl -4- hydroxy piperidine) succinate, bis- (2,2,6,6- tetramethyl -4- piperidyl) sebacic acid esters, certain herbaceous plants with big flowers One of double 1- octyloxy -2,2,6,6- tetramethyl piperidine alcohol esters of diacid and its more than;The antioxidant is β (3,5- bis- Tert-butyl-hydroxy phenyl) propionate, 3,5- di-tert-butyl-hydroxy phenyl propionic acid octadecanol ester, N, N- Double-[β (3,5- di-tert-butyl-hydroxy phenyl) propionyl] -1,6- hexamethylene diamine, (the 3- tertiary butyl-4-hydroxy-of triethylene glycol ether-two 5- aminomethyl phenyl) propionic ester, (3,5- di-tert-butyl-4-hydroxyl benzyl) the 1,3,5- triazine of 1,3,5- tri- -2,4,6- (1H, 3H, 5H)-triketone, three (2,4- di-tert-butyl-phenyl) phosphite esters, bis- (3,5- di-tert-butyl-phenyl) pentaerythritol diphosphites, Any one or more in 3,3- propane thioic acid laurel alcohol ester.
7. a kind of vehicle glass quick assembling one-component silane modified polyether seal glue as described in claim 1, feature It is, the deicer is in vinyltrimethoxysilane, vinyltriethoxysilane and vinyl dimethoxysilane Any one or more;The crosslinking agent is ethyl orthosilicate.
8. a kind of vehicle glass quick assembling one-component silane modified polyether seal glue as described in claim 1, feature It is, the coupling agent is gamma-aminopropyl-triethoxy-silane, γ-aminopropyltrimethoxysilane, N- β-(aminoethyl)-γ- Aminopropyl trimethoxysilane and N- β-(aminoethyl)-γ-aminopropyltriethoxy dimethoxysilane, 1146、6651, γ mercaptopropyitrimethoxy silane, γ-Mercaptopropyltriethoxysilane, γ-glycidol Ether oxygen propyl trimethoxy silicane, γ-glycidoxypropyltrietandysilane andysilane, γ-methacryloxypropyl three Any one or more in methoxy silane.
9. a kind of vehicle glass quick assembling one-component silane modified polyether seal glue as described in claim 1, feature Be, the catalyst be more alcoxyl fundamental mode titanate esters, Bis(lauroyloxy)dioctyltin, bis- (acetopyruvic acid) dibutyl tins with Any one or more in bis- (beta-diketo-ester) complexs of dialkoxy titanium.
10. a kind of vehicle glass quick assembling as described in any one of claims 1-9 is close with one-component silane modified polyether The preparation method of sealing, which comprises the steps of:
Step 1: filler and supporting material is 2.5~3.5 hours dry under the conditions of 110 DEG C~130 DEG C, it is spare;
Step 2: silane modified polyether resin, environment-friendlyplasticizer plasticizer, thixotropic agent, filler, supporting material are sequentially added in planet kettle And the deicer that mass fraction is 15~25%, high speed dispersion 30min~40min;Then vacuum degree be -0.09MPa~- 20min~30min is stirred under conditions of 0.1MPa;
Step 3: sequentially adding ultraviolet absorber, light stabilizer, antioxidant, ethyl orthosilicate, coupling agent, mass fraction is 75%~85% deicer and catalyst are simultaneously uniformly mixed, and are stirred under conditions of vacuum degree is -0.09MPa~-0.1MPa 20min~40min is mixed, is discharged up to product.
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CN113930205A (en) * 2021-10-28 2022-01-14 广州集泰化工股份有限公司 Sealant for refrigerated container
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CN110499136A (en) * 2019-08-21 2019-11-26 濮阳市万泉化工有限公司 A kind of automobile single-component silane-modified polyurethane sealant of weatherability
CN110894413A (en) * 2019-12-12 2020-03-20 湖南柯盛新材料有限公司 MS sealant with high filler content and preparation method and application thereof
CN111393966A (en) * 2020-04-28 2020-07-10 杭州之江新材料有限公司 Solvent-free silane-terminated modified polyether three-proofing paint and preparation method thereof
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CN113930205A (en) * 2021-10-28 2022-01-14 广州集泰化工股份有限公司 Sealant for refrigerated container
CN113930205B (en) * 2021-10-28 2023-08-15 广州集泰化工股份有限公司 Sealant for refrigerated container
CN115558461A (en) * 2022-02-14 2023-01-03 安徽牛元新材料有限公司 Single-component elastic binder for rock plate and preparation method thereof
CN115558461B (en) * 2022-02-14 2023-08-15 安徽牛元新材料有限公司 Single-component elastic binder for rock plate and preparation method thereof

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