CN104650306B - Acrylate acrylamide kind block polymer and its synthetic method and application - Google Patents
Acrylate acrylamide kind block polymer and its synthetic method and application Download PDFInfo
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- CN104650306B CN104650306B CN201510018765.2A CN201510018765A CN104650306B CN 104650306 B CN104650306 B CN 104650306B CN 201510018765 A CN201510018765 A CN 201510018765A CN 104650306 B CN104650306 B CN 104650306B
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Abstract
The invention belongs to high molecular polymer field, a kind of acrylate acrylamide kind block polymer and its synthetic method and application are disclosed.The acrylate acrylamide kind block polymer is prepared from by lauryl methacrylate and N (3 dimethylamino-propyl) Methacrylamide with RAFT polymerizations.Its synthetic method comprises the following steps:Under oxygen free condition, monomer methacrylic acid lauryl (or N (3 dimethylamino-propyl) Methacrylamide) is in the presence of initiator and RAFT reagents, generation RAFT reagent macromoleculars, acted on monomer N (3 dimethylamino-propyl) Methacrylamide (or lauryl methacrylate) again, generation acrylate acrylamide kind block polymer is reacted under the induction of initiator.Inorganic particle surfaces are covered the acrylate acrylamide kind block polymer and encapsulating effect is good, dispersion stabilization, can be applied to the dispersion of ceramic ink jet ink.
Description
Technical field
The invention belongs to ink-jet ink technology of preparing and high molecular polymer field, and in particular to a kind of acrylate-the third
Acrylamide block polymer and its synthetic method and application.
Background technology
Ceramic ink jet printing technology is the most top technology in present ceramic surface decoration technique field, is by ceramic paint powder
System is directly printed on stock it by ink-jet printer into ceramic ink, is molded through high-temperature process.Due to this system
The geometry of the incrustation that Preparation Method is carried out is the plastic complicated shape product by computer software control, and is departed from
Mould limitation, therefore can greatly shorten the mechanical process of other mode of printings.Due to its particularity, inkjet printing is realized
Key be ceramic ink preparation.
Ceramic ink is generally made up of ceramic paint particle, solvent, dispersant and other auxiliary agents, and ceramic paint particle is ink
The core substance of water, in order to ensure the dispersion stabilization of paint ink, reduces the operating troubles such as plug nozzle, usually requires that pigment
The particle diameter of particle is less than 1 μm, and dispersant can ensure the dispersion that ceramic paint powder can be uniform and stable in a solvent, is come with this
Ensure that the ceramic ink for preparing was not reunited before spraying.As can be seen here, stably dispersing of the dispersant to ceramic ink
Property plays decisive role.
Effect of the dispersant to ceramic pigment is mainly realized by following three kinds of modes:
(1) electrostatic stabilization is theoretical:Increase the absolute value of ceramic pigment particle surface current potential, improve intergranular electrostatic stabilization
Effect;(2) spatial stability is theoretical:By steric hindrance of the macromolecule dispersing agent between the adsorption layer that ceramic pigment particle surface is formed
Effect, makes to produce very strong steric hindrance repulsive force between particle;(3) regulate and control ceramic pigment particle surface polarity, both strengthen decentralized medium
To its wetability, surface solvent film is enhanced again, improve grain surface texture degree, make structuring repulsive force significantly
Enhancing.
Dispersant can effectively prevent the coagulation of ceramic ink, and its reasonable selection and content are crucial.
Macromolecule dispersing agent is the efficient polymeric dispersant of a class, due to its excellent performance, is led in ink and coating
Vital effect is played in domain.Compared with traditional dispersant, macromolecule dispersing agent can accelerate surface of pigments wetting, shorten
The time required to grinding, ink viscosity is reduced, the tinctorial strength of ink or coating can also be increased, increase the solid content of system, most
It is important that being also may rely on its powerful solid space effect, dispersion stabilization of the pigment in organic media is improved.Block is high
Compared with random copolymer dispersant, the former has preferably moistening peptizaiton to granules of pigments to dispersal agent molecule;And block is combed
Type copolymer dispersant has more preferable absorption stability, dispersion stabilization than simple block copolymer dispersant.
The research such as Zhou Songqing finds that with polyvinyl alcohol as dispersant the addition of dispersant is 0.1%, and shitosan is bonding
Agent, when addition is 0.08%, the stability and other physicochemical properties of the black ceramic ink of preparation are optimal;
The macromolecule dispersing agent PMAA-mPEO of the synthesis such as Yoshikawa, research display, to BaTiO3Suspended substance has good dispersion
Stability.
Mainly there are ICI, KvK, Dupont, BASF, BYK in external exploitation at present, the company of development macromolecule dispersing agent,
The companies such as Daniel, SunChemical.The domestic research to macromolecule dispersing agent is started late, and dispersant is few, synthesis side
Method is also immature, and the product performance of its exploitation cannot also fully meet use requirement, still need to a large amount of import external products.Cause
This, the macromolecule dispersing agent of exploitation and development function admirable is significant
The content of the invention
In order to overcome the shortcoming and deficiency of prior art, primary and foremost purpose of the invention is to provide a kind of acrylate-the third
Acrylamide block polymer;
Synthetic method another object of the present invention is to provide aforesaid propylene acid esters-acrylamide kind block polymer;
It is still another object of the present invention to provide the application of aforesaid propylene acid esters-acrylamide kind block polymer.
The purpose of the present invention is achieved through the following technical solutions:
A kind of acrylate-acrylamide kind block polymer, it is by monomer methacrylic acid lauryl (LMA) and monomer
N- (3- dimethylamino-propyls) Methacrylamide (DMAPMA) polymerizations are prepared from, with following structure:
Wherein, m is 10~50 integral multiple, and n is 10~50 integral multiple.
Aforesaid propylene acid esters-acrylamide kind block polymer is according to monomer methacrylic acid lauryl and monomer N- (3-
Dimethylamino-propyl) Methacrylamide the order for carrying out RAFT polymerizations it is different, include two kinds of synthetic methods.
The first synthetic method of aforesaid propylene acid esters-acrylamide kind block polymer, comprises the following steps:Anaerobic bar
Under part, monomer methacrylic acid lauryl (LMA) generates RAFT reagent macromoleculars in the presence of initiator and RAFT reagents,
Acted on monomer N- (3- dimethylamino-propyls) Methacrylamide (DMAPMA) again, generation P is reacted under the induction of initiator
(DMAPMA)-b-P (LMA) copolymer, as described acrylate-acrylamide kind block polymer;
The first synthetic method of aforesaid propylene acid esters-acrylamide kind block polymer, specifically includes following steps:
A be added in reactor for lauryl methacrylate (LMA), RAFT reagents, initiator M and solvent orange 2 A by (), stirring
It is uniform to obtain mixed liquor;Under condition of ice bath, reactor leads to nitrogen, and being then warming up to reaction temperature under oil bath is reacted, and is reached
Fast cooling and in the air after to the reaction time, stops reaction, and reaction products therefrom purify obtaining centre
Product LMA macro-RAFT;
B () is by intermediate product LMA macro-RAFT, monomer N- (3- dimethylamino-propyls) Methacrylamide
(DMAPMA), initiator N and solvent B are added in reactor, and stir to obtain mixed reaction solution;Under condition of ice bath, reaction
Device leads to nitrogen, and being then warming up to reaction temperature under oil bath is reacted, and reaches after the reaction time fast cooling and exposed to sky
In gas, stop reaction, reaction products therefrom purify and obtains final product P (DMAPMA)-b-P (LMA), it is as described
Acrylate-acrylamide kind block polymer.
In the first synthetic method of aforesaid propylene acid esters-acrylamide kind block polymer,
Preferably, step (a) the RAFT reagents are asymmetric trithiocarbonate, specially S- ethyls-S '-(2- first
Base propionic acid) trithiocarbonate or S- dodecyls-S '-(2 Methylpropionic acid) trithiocarbonate;
Preferably, step (a) the initiator M is azodiisobutyronitrile (AIBN);
Preferably, step (a) solvent orange 2 A is ethyl acetate, toluene or DMF (DMF);
Preferably, step (a) reaction temperature is 60~80 DEG C, and the reaction time is 8~24h;
Preferably, in step (a) mixed liquor lauryl methacrylate, RAFT reagents and initiator M mol ratio
It is 33:1:0.1~500:1:0.3, mass fraction of the lauryl methacrylate in step (a) mixed liquor is 10%;
Preferably, step (b) the initiator N is azodiisobutyronitrile (AIBN);
Preferably, step (b) the solvent B is DMF (DMF);
Preferably, step (b) reaction temperature is 60~80 DEG C, and the reaction time is 12~24h;
Preferably, step (a) and step (b) fast cooling are lowered the temperature using ice bath;
Preferably, the Methacrylamides of N- (3- dimethylamino-propyls) described in step (b) mixed reaction solution, centre
The mol ratio of product LMA macro-RAFT and initiator N is 50:1:0.1~200:1:0.3, N- (3- dimethylamino-propyls) first
Mass fraction of the base acrylamide in step (b) mixed reaction solution is 10%.
Second synthetic method of aforesaid propylene acid esters-acrylamide kind block polymer, comprises the following steps:Anaerobic bar
Under part, in the presence of initiator and RAFT reagents, generation RAFT is tried monomer N- (3- dimethylamino-propyls) Methacrylamides
Agent macromolecular, then acted on monomer methacrylic acid lauryl, generation P (LMA)-b-P is reacted under the induction of initiator
(DMAPMA) copolymer, as described acrylate-acrylamide kind block polymer;
Second synthetic method of aforesaid propylene acid esters-acrylamide kind block polymer, specifically includes following steps:
(1) N- (3- dimethylamino-propyls) Methacrylamide (DMAPMA), RAFT reagents, initiator P and solvent C are added
Enter in reactor, stir to obtain mixed liquor;Under condition of ice bath, reactor leads to nitrogen, is then warming up under oil bath anti-
Answer temperature to be reacted, reach after the reaction time fast cooling and in air, stop reaction, products therefrom will be reacted
Purify and obtain intermediate product DMAPMA macro-RAFT;
(2) by intermediate product DMAPMA macro-RAFT, monomer methacrylic acid lauryl (LMA), initiator Q and molten
Agent D is added in reactor, and stir to obtain mixed reaction solution;Under condition of ice bath, reactor leads to nitrogen, then under oil bath
It is warming up to reaction temperature to be reacted, reaches after the reaction time fast cooling and in air, stop reaction, will reacts
Products therefrom purify and obtains final product P (LMA)-b-P (DMAPMA), and as described acrylate-acrylic amide is embedding
Section polymer.
In second synthetic method of aforesaid propylene acid esters-acrylamide kind block polymer,
Preferably, step (1) the RAFT reagents are asymmetric trithiocarbonate, specially S- ethyls-S '-(2- first
Base propionic acid) trithiocarbonate or S- dodecyls-S '-(2 Methylpropionic acid) trithiocarbonate;
Preferably, step (1) the initiator P is azodiisobutyronitrile (AIBN);
Preferably, step (1) described solvent C is ethyl acetate, toluene or DMF (DMF);
Preferably, step (1) described reaction temperature is 60~80 DEG C, and the reaction time is 8~24h;
Preferably, N- (3- dimethylamino-propyls) Methacrylamide, RAFT reagents and draw in step (1) described mixed liquor
The mol ratio of hair agent P is 50:1:0.1~200:1:0.3, N- (3- dimethylamino-propyls) Methacrylamide is in step (1) institute
It is 10% to state the mass fraction in mixed liquor;
Preferably, step (2) the initiator Q is azodiisobutyronitrile (AIBN);
Preferably, step (2) the solvent D is DMF (DMF);
Preferably, step (2) described reaction temperature is 60~80 DEG C, and the reaction time is 12~24h;
Preferably, step (1) and step (2) fast cooling are lowered the temperature using ice bath;
Preferably, lauryl methacrylate, intermediate product DMAPMA macro- in step (2) described mixed reaction solution
The mol ratio of RAFT and initiator Q is 33:1:0.1~500:1:0.3, lauryl methacrylate is in step (2) mixing
Mass fraction in reaction solution is 10%.
Aforesaid propylene acid esters-acrylamide kind block polymer can be applied to ceramic ink jet ink preparing technical field;Tool
Body can be used to disperse the ceramic pigment in ceramic ink jet ink.
Principle of the invention:
In solvent-solid dispersion system, a certain amount of hydroxyl is contained on ceramic paint particle (metal oxide) surface, this
Invent the acrylate-acrylamide kind block polymer to be fully contacted with ceramic pigment surface, the acrylate-propylene
Anchoring group [- N (the CH of acid amides kind block polymer3)] interact to form hydrogen bond with the hydroxyl on colorant, form one layer of cause
Close and firm clad, the clad can make pigment granules surface organic;On the other hand, the acrylate-acryloyl
The hydrocarbon chain of amine block polymer lauryl can form protective layer as solvent chain on pigment granules surface, extend in solvent
In.When pigment granules are close to each other, the acrylate-acrylamide kind block polymer plays steric hindrance effect,
Grain is mutually exclusive due to steric hindrance effect, ceramic paint dispersion stabilization in a solvent is increased, so that ceramic ink
Water energy stable existence.
Acrylate of the present invention-acrylamide kind block polymer is used as ceramic ink macromolecule dispersing agent, by
In the advantage of its structure, can significantly more efficient dispersed ceramic granules of pigments.
The present invention has the following advantages and effect relative to prior art:
(1) acrylate of the present invention-acrylamide kind block polymer is used as ceramic ink dispersant to ceramics
Surface of pigments cover and encapsulating effect will more preferably, dispersion it is more stable.
(2) acrylate of the present invention-acrylamide kind block polymer, has more than homopolymers or random copolymer
Good dispersed inorganic particles.
(3) synthetic method of the present invention is RAFT polymerizations, can preferably control molecular weight and its distribution of polymer, than
The polymer of conventional free radical polymerization has more excellent structure;Strong adaptability, may be used on the dispersion of various inorganic particles.
(4) synthesising method reacting condition of the present invention is gentle, and synthesis technique is simple.
Specific embodiment
With reference to embodiment, the present invention is described in further detail, but embodiments of the present invention not limited to this.
Embodiment 1
A kind of acrylate-acrylamide kind block polymer, with following structure:
Wherein, m is that 32, n is 41;
The synthetic method of the acrylate-acrylamide kind block polymer comprises the following steps:
(1) by 25.44g lauryl methacrylates (LMA) (0.10mol), 0.364g RAFT reagent S- dodecyls-
S '-(2 Methylpropionic acid) trithiocarbonate (0.001mol), 0.016g initiator azodiisobutyronitriles (AIBN) (1 × 10- 4Mol) it is added in reactor with 228.96g toluene, stirring mixing;Under condition of ice bath, reactor leads to nitrogen 40min to remove
Remove air, 75 DEG C are then warming up under oil bath is reacted, reaction 15h after fast cooling and be exposed to air in, make reaction
Stop, reaction products therefrom purify and obtains intermediate product LMA macro-RAFT;
(2) by 10.43g intermediate product LMA macro-RAFT, 17.02g monomers N- (3- dimethylamino-propyls) methyl-prop
Acrylamide (DMAPMA) (0.10mol), 0.016g initiator As IBN (1 × 10-4) and 153.18g DMF are added to reactor mol
In, stirring mixing;Under condition of ice bath, the logical nitrogen 40min of reactor is warming up to 75 DEG C under oil bath and enters to remove air, then
Row reaction, fast cooling and in the air after reaction 24h, stops reaction, will react products therefrom and be purified
Final product P (DMAPMA)-b-P (LMA), as described acrylate-acrylamide kind block polymer.
Embodiment 2
A kind of acrylate-acrylamide kind block polymer, with following structure:
Wherein, m is that 29, n is 37;
The synthetic method of the acrylate-acrylamide kind block polymer comprises the following steps:
(1) by 25.44g lauryl methacrylates (LMA) (0.10mol), 0.364g RAFT reagent S- dodecyls-
S '-(2 Methylpropionic acid) trithiocarbonate (0.001mol), 0.033g initiator azodiisobutyronitriles (AIBN) (2 × 10- 4Mol) it is added in reactor with 228.96g ethyl acetate, stirring mixing;Under condition of ice bath, the logical nitrogen 40min of reactor
To remove air, 80 DEG C are then warming up under oil bath and are reacted, reaction 20h after fast cooling and be exposed to air in, make
Reaction stops, and purify and obtain intermediate product LMA macro-RAFT reaction products therefrom;
(2) by 9.41g intermediate product LMA macro-RAFT, 8.51g monomers N- (3- dimethylamino-propyls) metering system
Acid amides (DMAPMA) (0.05mol), 0.033g initiator As IBN (2 × 10-4Mol) it is added in reactor with 76.59g DMF,
Stirring mixing;Under condition of ice bath, the logical nitrogen 40min of reactor is warming up to 80 DEG C to remove air, then under oil bath to be carried out
Reaction, fast cooling and in the air after reaction 24h, stops reaction, will react products therefrom and be purified most
End-product P (DMAPMA)-b-P (LMA), as described acrylate-acrylamide kind block polymer.
Embodiment 3
A kind of acrylate-acrylamide kind block polymer, with following structure:
Wherein, m is that 24, n is 32;
The synthetic method of the acrylate-acrylamide kind block polymer comprises the following steps:
(1) by 25.44g lauryl methacrylates (LMA) (0.10mol), 0.364g RAFT reagent S- dodecyls-
S '-(2 Methylpropionic acid) trithiocarbonate (0.001mol), 0.049g initiator azodiisobutyronitriles (AIBN) (3 × 10- 4Mol) it is added in reactor with 228.96g DMF, stirring mixing;Under condition of ice bath, reactor leads to nitrogen 40min to remove
Remove air, 75 DEG C are then warming up under oil bath is reacted, reaction 24h after fast cooling and be exposed to air in, make reaction
Stop, reaction products therefrom purify and obtains intermediate product LMA macro-RAFT;
(2) by 8.14g intermediate product LMA macro-RAFT, 8.51g monomers N- (3- dimethylamino-propyls) metering system
Acid amides (DMAPMA) (0.05mol), 0.049g initiator As IBN (3 × 10-4Mol) it is added in reactor with 100g DMF, is stirred
Mix mixing;Under condition of ice bath, to remove air, 75 DEG C are then warming up under oil bath is carried out anti-the logical nitrogen 40min of reactor
Should, fast cooling and in the air after reaction 24h stops reaction, and reaction products therefrom purify and obtained finally
Product P (DMAPMA)-b-P (LMA), as described acrylate-acrylamide kind block polymer.
Embodiment 4
A kind of acrylate-acrylamide kind block polymer, with following structure:
Wherein, m is that 30, n is 45;
The synthetic method of the acrylate-acrylamide kind block polymer comprises the following steps:
(1) by 17.03g N- (3- dimethylamino-propyls) Methacrylamide (DMAPMA) (0.10mol), 0.364g
S- dodecyls-S '-(2 Methylpropionic acid) trithiocarbonate (0.001mol), 0.016g initiator azodiisobutyronitriles (1 ×
10-4Mol) it is added in reactor with 153.27g toluene, stirring mixing;Under condition of ice bath, the logical nitrogen 40min of reactor with
Air is removed, 70 DEG C is then warming up under oil bath and is reacted, fast cooling and in the air after reaction 15h makes instead
Should stop, reaction products therefrom purify and obtains intermediate product DMAPMA macro-RAFT;
(2) by 7.66g intermediate products DMAPMA macro-RAFT, 25.44g monomer methacrylic acids lauryl (LMA)
(0.10mol), 0.016g initiator As IBN (1 × 10-4Mol) it is added in reactor with 100g DMF, stirring mixing;In ice bath
Under the conditions of, the logical nitrogen 40min of reactor is warming up to 70 DEG C under oil bath and is reacted to remove air, then, fast after reaction 24h
Prompt drop temperature simultaneously in the air, stops reaction, purify and obtain final product P (LMA)-b-P reaction products therefrom
(DMAPMA), as described acrylate-acrylamide kind block polymer.
Embodiment 5
A kind of acrylate-acrylamide kind block polymer, with following structure:
Wherein, m is that 28, n is 30;
The synthetic method of the acrylate-acrylamide kind block polymer comprises the following steps:
(1) by 8.51g N- (3- dimethylamino-propyls) Methacrylamide (DMAPMA) (0.05mol), the S- of 0.363g
Dodecyl-S '-(2- methyl) propionic acid trithiocarbonate (0.001mol), 0.033g initiator azodiisobutyronitriles (2 ×
10-4Mol) it is added in reactor with 76.59g ethyl acetate, stirring mixing;Under condition of ice bath, the logical nitrogen 40min of reactor
To remove air, 80 DEG C are then warming up under oil bath and are reacted, reaction 20h after fast cooling and be exposed to air in, make
Reaction stops, and purify and obtain intermediate product DMAPMA macro-RAFT reaction products therefrom;
(2) by 5.1l g intermediate products DMAPMA macro-RAFT, 25.44g monomer methacrylic acids lauryl (LMA)
(0.10mol), 0.033g initiator As IBN (2 × 10-4Mol) it is added in reactor with 228.96g DMF, stirring mixing;
Under condition of ice bath, the logical nitrogen 40min of reactor is warming up to 80 DEG C under oil bath and is reacted to remove air, then, reacts 24h
Fast cooling and in the air, stops reaction afterwards, will reaction products therefrom purify obtain final product P (LMA)-
B-P (DMAPMA), as described acrylate-acrylamide kind block polymer.
Embodiment 6
A kind of acrylate-acrylamide kind block polymer, with following structure:
Wherein, m is that 51, n is 27;
The synthetic method of the acrylate-acrylamide kind block polymer comprises the following steps:
(1) by 8.51g N- (3- dimethylamino-propyls) Methacrylamide (DMAPMA) (0.05mol), the S- of 0.364g
Dodecyl-S '-(2 Methylpropionic acid) trithiocarbonate (0.001mol), 0.049g initiator azodiisobutyronitriles (3 ×
10-4Mol) it is added in reactor with 76.59g DMF, stirring mixing;Under condition of ice bath, reactor leads to nitrogen 40min to remove
Remove air, 75 DEG C are then warming up under oil bath is reacted, reaction 24h after fast cooling and be exposed to air in, make reaction
Stop, reaction products therefrom purify and obtains intermediate product DMAPMA macro-RAFT;
(2) by 4.61g intermediate products DMAPMA macro-RAFT, 31.80g monomer methacrylic acids lauryl (LMA)
(0.125mol), 0.049g initiator As IBN (3 × 10-4Mol) it is added in reactor with 286.2g DMF, stirring mixing;
Under condition of ice bath, the logical nitrogen 40min of reactor is warming up to 75 DEG C under oil bath and is reacted to remove air, then, reacts 24h
Fast cooling and in the air, stops reaction afterwards, purify and obtain final product P reaction products therefrom
(DMAPMA)-b-P (LMA), as described acrylate-acrylamide kind block polymer.
Dispersive property of each embodiment gained acrylate-acrylamide kind block polymer in ceramic ink jet ink is surveyed
Examination:
Commercially available ceramic paint is added in container, be subsequently adding acrylate that organic solvent synthesizes with each embodiment-
Acrylamide kind block polymer, digital display viscosity apparatus test system viscosity is used after being well mixed, and with 10mL ground colorimetric cylinders
The dispersion stabilization of test system, test acquired results are as shown in table 1.
1 acrylate of table-influence of the acrylamide kind block polymer to ceramic paint particle viscosity and dispersion stabilization
As it can be seen from table 1 acrylate of the present invention-acrylamide kind block polymer covers to ceramic paint surface
Lid and encapsulating effect are good, dispersion stabilization, the holding time for that can extend ceramic ink in ceramic ink, while effectively
The viscosity of ceramic ink is reduced, inkjet printing is complied with.
Above-described embodiment is the present invention preferably implementation method, but embodiments of the present invention are not by above-described embodiment
Limitation, it is other it is any without departing from Spirit Essence of the invention and the change, modification, replacement made under principle, combine, simplification,
Equivalent substitute mode is should be, is included within protection scope of the present invention.
Claims (7)
1. acrylate-application of the acrylamide kind block polymer in ceramic ink jet technical field, it is characterised in that:It is described
Acrylate-acrylamide kind block polymer is applied to ceramic ink jet ink preparing technical field as macromolecule dispersing agent;
The acrylate-acrylamide kind block polymer is by monomer methacrylic acid lauryl and monomer N- (3- dimethylaminos third
Base) Methacrylamide polymerization be prepared from, with following structure:
Wherein, m is 10~50 integer, and n is 10~50 integer.
2. acrylate according to claim 1-acrylamide kind block polymer is in ceramic ink jet technical field
Using, it is characterised in that the acrylate-acrylamide kind block polymer is prepared via a method which to obtain:Anaerobic bar
Under part, monomer methacrylic acid lauryl in the presence of initiator and RAFT reagents, generate RAFT reagent macromoleculars, then with list
Body N- (3- dimethylamino-propyls) Methacrylamide is acted on, and generation P (DMAPMA)-b-P is reacted under the induction of initiator
(LMA) copolymer, as described acrylate-acrylamide kind block polymer.
3. acrylate according to claim 2-acrylamide kind block polymer is in ceramic ink jet technical field
Using, it is characterised in that the acrylate-acrylamide kind block polymer is prepared via a method which to obtain:
A be added in reactor for lauryl methacrylate, RAFT reagents, initiator M and solvent orange 2 A by (), stirring to mix
Close liquid;Under condition of ice bath, reactor leads to nitrogen, and being then warming up to reaction temperature under oil bath is reacted, when reaching reaction
Between after fast cooling and in the air, stop reaction, products therefrom will be reacted purify and obtain intermediate product LMA
macro-RAFT;
(b) by intermediate product LMA macro-RAFT, monomer N- (3- dimethylamino-propyls) Methacrylamide, initiator N and
Solvent B is added in reactor, and stir to obtain mixed reaction solution;Under condition of ice bath, reactor leads to nitrogen, then in oil bath
Under be warming up to reaction temperature and reacted, reach after the reaction time fast cooling and in air, stop reaction, will be anti-
Answering products therefrom purify and obtains final product P (DMAPMA)-b-P (LMA), as described acrylate-acrylic amide
Block polymer.
4. acrylate according to claim 3-acrylamide kind block polymer is in ceramic ink jet technical field
Using, it is characterised in that:Step (a) the RAFT reagents are asymmetric trithiocarbonate;Step (a) the initiator M is
Azodiisobutyronitrile;Step (a) solvent orange 2 A is ethyl acetate, toluene or N,N-dimethylformamide;Step (a) is described anti-
It is 60~80 DEG C to answer temperature, and the reaction time is 8~24h;Lauryl methacrylate in step (a) mixed liquor,
The mol ratio of RAFT reagents and initiator M is 33:1:0.1~500:1:0.3, lauryl methacrylate is described in step (a)
Mass fraction in mixed liquor is 10%;
Step (b) the initiator N is azodiisobutyronitrile;Step (b) the solvent B is N,N-dimethylformamide;Step
B () described reaction temperature is 60~80 DEG C, the reaction time is 12~24h;N- described in step (b) mixed reaction solution
The mol ratio of (3- dimethylamino-propyls) Methacrylamide, intermediate product LMA macro-RAFT and initiator N is 50:1:
0.1~200:1:Quality of 0.3, N- (3- dimethylamino-propyls) Methacrylamide in step (b) mixed reaction solution
Fraction is 10%.
5. acrylate according to claim 1-acrylamide kind block polymer is in ceramic ink jet technical field
Using, it is characterised in that the acrylate-acrylamide kind block polymer is prepared via a method which to obtain:Anaerobic bar
Under part, in the presence of initiator and RAFT reagents, generation RAFT is tried monomer N- (3- dimethylamino-propyls) Methacrylamides
Agent macromolecular, then acted on monomer methacrylic acid lauryl, generation P (LMA)-b-P is reacted under the induction of initiator
(DMAPMA) copolymer, as described acrylate-acrylamide kind block polymer.
6. acrylate according to claim 5-acrylamide kind block polymer is in ceramic ink jet technical field
Using, it is characterised in that the acrylate-acrylamide kind block polymer is prepared via a method which to obtain:
(1) N- (3- dimethylamino-propyls) Methacrylamide, RAFT reagents, initiator P and solvent C are added to reactor
In, stir to obtain mixed liquor;Under condition of ice bath, reactor leads to nitrogen, and reaction temperature is then warming up under oil bath is carried out
Reaction, reaches after the reaction time fast cooling and in air, stops reaction, and will react products therefrom purify
To intermediate product DMAPMA macro-RAFT;
(2) intermediate product DMAPMA macro-RAFT, monomer methacrylic acid lauryl, initiator Q and solvent D are added to
In reactor, stir to obtain mixed reaction solution;Under condition of ice bath, reactor leads to nitrogen, is then warming up under oil bath anti-
Answer temperature to be reacted, reach after the reaction time fast cooling and in air, stop reaction, products therefrom will be reacted
Purify and obtain final product P (LMA)-b-P (DMAPMA), as described acrylate-acrylamide kind block polymer.
7. acrylate according to claim 6-acrylamide kind block polymer is in ceramic ink jet technical field
Using, it is characterised in that:Step (1) the RAFT reagents are asymmetric trithiocarbonate;Step (1) the initiator P is
Azodiisobutyronitrile;Step (1) described solvent C is ethyl acetate, toluene or N,N-dimethylformamide;Step (1) is described anti-
It is 60~80 DEG C to answer temperature, and the reaction time is 8~24h;N- (3- dimethylamino-propyls) first in step (1) described mixed liquor
The mol ratio of base acrylamide, RAFT reagents and initiator P is 50:1:0.1~200:1:0.3, N- (3- dimethylamino-propyls)
Mass fraction of the Methacrylamide in step (1) described mixed liquor is 10%;
Step (2) the initiator Q is azodiisobutyronitrile;Step (2) the solvent D is N,N-dimethylformamide;Step
(2) reaction temperature is 60~80 DEG C, and the reaction time is 12~24h;Methyl-prop in step (2) described mixed reaction solution
The mol ratio of olefin(e) acid lauryl, intermediate product DMAPMA macro-RAFT and initiator Q is 33:1:0.1~500:1:0.3, first
Mass fraction of the base lauryl acrylate in step (2) described mixed reaction solution is 10%.
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