CN100462381C - Acrylic acid bulk hybridization emulsion composition - Google Patents
Acrylic acid bulk hybridization emulsion composition Download PDFInfo
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- CN100462381C CN100462381C CNB200610109443XA CN200610109443A CN100462381C CN 100462381 C CN100462381 C CN 100462381C CN B200610109443X A CNB200610109443X A CN B200610109443XA CN 200610109443 A CN200610109443 A CN 200610109443A CN 100462381 C CN100462381 C CN 100462381C
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Abstract
the invention discloses a hybridized emulsion composition of acrylic bulk, which comprises the following parts: acrylic monomer, oiliness acrylic resin, modified resin, surfactant, initiator, neutralizer, deionized water, chain transition agent and solutizer, wherein the oiliness acrylic resin, modified resin and oiliness initiator are dissolved in the solutizer with acrylic monomer to obtain monomer solution, which is dissolved in the deionized water to produce initiator composition to prepare hybridized emulsion composition through polymeric reaction.
Description
Technical field
The present invention relates to a kind of acrylic acid bulk hybridization emulsion polymeric method.
Background technology
Along with the attention of people to environmental protection, the content of control VOC, industrial water-borne coatings will replace the use of oil paint in a large number, but water-borne coatings is at gloss, water tolerance, and aspects such as sticking power are difficult to reach the performance of oil paint all the time.Water-borne acrylic resin has soon advantages such as the not yellowing of doing, film, but film chemical proof and water tolerance are relatively poor, can not replace the oiliness acrylic resin to use in a lot of fields, if the oiliness acrylic resin is carried out the hybridisation emulsion polymerization with acrylic monomer in aqueous medium, make stable hybridisation emulsion system, this type of emulsion had both had the characteristics of oleoresin, was again solvent with water, compliance with environmental protection requirements.This type of emulsion can be widely used in industrial antisepsis, building coating, coatings for furniture and frie retardant coating etc.
Present existing hybridisation emulsion is an allosome hydridization all generally, as epoxy-vinylformic acid, and alkyd-vinylformic acid, urethane-vinylformic acid, polyester-vinylformic acid etc.Existing hydridization technology generally is divided into two kinds: physical blending and graft copolymerization, but these two kinds of methods are inapplicable in acrylic acid bulk hybridization emulsion, at first the method for physical blending is that polymer emulsion with the different chemical component carries out composite, but because stability of the system after the blend and uniformity are poor, so on performance, still can not reach the required purpose of hydridization; And graft copolymerization is promptly carried out grafting by the macromole that polyreaction will have a difference in functionality, and this just requires to participate in to have the unsaturated group that can participate in polyreaction in a large number on the macromole of hydridization, forms the graft polymerization system.Practical situation according to the acrylic acid bulk hybridization emulsion system, this invention adopts the reaction blending means, by suitable synthesis technique, prepared a kind of novel water miscible liquid, make two kinds of polymer macromolecules pass through the crosslinked or grafting formation half interpenetrating network structure of small part, guarantee that two kinds of polymkeric substance finely disseminated this hybridisation emulsion of giving simultaneously in a mixture brings excellent more performance.
Summary of the invention
Utilize the oiliness acrylic resin in aqueous medium, to carry out the hybridisation emulsion polymerization, made stable hybridisation emulsion system with acrylic monomer.This type of emulsion had both had the characteristics of oleoresin, as high gloss, and water-tolerant, characteristics such as strong adhesion are again solvent with water, compliance with environmental protection requirements.
Adopt the reaction blending means, guarantee two kinds of polymkeric substance good dispersion in a mixture.Make polymkeric substance 1 and 2 produce a kind of interpenetrating(polymer)networks, perhaps stricter saying is a kind of crosslinked or grafted semi-intercrossing network of small part that has only.
Acrylic acid bulk hybridization emulsion of the present invention, it is by following material proportioning synthetic:
Parts by weight of raw materials
Acrylic monomer 20～40
Oiliness acrylic resin 5～20
Modified resin 1～5
Tensio-active agent 5～15
Initiator 0.1～0.3
Neutralizing agent 0.1～0.5
Deionized water 30～60
Chain-transfer agent 0.5～5
Solubility promoter 5～15
Described acrylic monomer comprise following one or more: vinylformic acid, methacrylic acid, methyl methacrylate, methyl acrylate, ethyl propenoate, Hydroxyethyl acrylate, Propylene glycol monoacrylate, butyl acrylate, butyl methacrylate, Propenoic acid, 2-methyl, isobutyl ester, ethyl acrylate etc.
Described oiliness acrylic resin is as hybrid resin, its molecular weight between 40000～100000, the oiliness acrylic resin of second-order transition temperature between 30 ℃～60 ℃.Comprise following one or more: the copolymer resins of copolymer resins, methacrylic ester and the vinyl cyanide of the copolymer resins of the homopolymerization resin of acrylate, the homopolymerization resin of methacrylic ester, acrylate, copolymer resins, acrylate and cinnamic copolymer resins, methacrylic ester and cinnamic copolymer resins, acrylate and the vinyl cyanide of methacrylic ester.
Described modified resin is urethane resin, Synolac and Resins, epoxy etc.
Described tensio-active agent comprises: anion surfactant, nonionic surface active agent, negatively charged ion and non-ionic composite tensio-active agent and partial reaction type tensio-active agent.
Described nonionic surface active agent comprises: polyoxyethylene nonylphenol ether, alkylphenol polyoxyethylene, polyoxyethylene octylphenol ether, polyoxyethylene nonylphenol ether, polyoxyethylene lauric acid ester, polyoxyethylene stearic acid ester.
Described aniorfic surfactant comprises: Sodium dodecylbenzene sulfonate, Witco 1298 Soft Acid ammonium, disodium 4-dodecyl-2,4 '-oxydibenzenesulfonate, sodium lauryl sulphate, sodium laurylsulfonate or their mixture.
Described negatively charged ion and non-ionic composite tensio-active agent comprise: fatty alkyd polyethenoxy ether sodium sulfate, nonylphenol polyoxyethylene ether sulfate, the ninth of the ten Heavenly Stems base polyoxyethylene ether ammonium sulfate.
Described response type surfactant active comprises: sodium p styrene sulfonate, acrylamide stearic acid sodium salt, alkyl vinylformic acid-2-ethanesulfonic acid sodium salt, maleic acid higher alcohols monoester sodium salt, the polycondensate of polyoxyethylene phenolic group in ninth of the ten Heavenly Stems ether, Succinic Acid and glycidyl methacrylate or polyoxyethylene phenolic ether in ninth of the ten Heavenly Stems acrylate.
Described initiator comprises following one or more: ammonium persulphate, Potassium Persulphate, benzoyl peroxide, Diisopropyl azodicarboxylate.
Described neutralizing agent comprises ammoniacal liquor, Triethylene Diamine, diethanolamine, trolamine, 2-amino-1-propyl alcohol, N-ethyl agate beautiful jade, N, N dimethylethanolamine, sodium bicarbonate, yellow soda ash as the pH value conditioning agent.
Described solubility promoter is used for improving the stability of system.Comprise: the various ether solvents that can dissolve each other with water.For example: propylene glycol monomethyl ether, propylene glycol butyl ether, dipropylene glycol methyl ether, tripropylene glycol methyl ether, dipropylene glycol dme, 1-Methoxy-2-propyl acetate.
Described chain-transfer agent is used for the molecular weight of controlling polymers, and chain-transfer agent commonly used comprises uncle's ten carbon mercaptan, uncle's DDM dodecyl mercaptan, tert-dodecyl mercaptan, uncle's 16 carbon mercaptan, the hot carbon mercaptan of uncle.
The preparation method of acrylic acid bulk hybridization emulsion of the present invention:
(1) at first prepare monomer solution: with the oiliness acrylic resin, modified resin and oil-soluble initiator are dissolved in acrylic monomer, and add the solubility promoter of metering, obtain monomer solution;
Initiator component: water soluble starter is dissolved in the deionized water.
(2) polyreaction: tensio-active agent that will part metering, initiator, neutralizing agent, chain-transfer agent, deionized water, and part propylene acids monomer add reactor as seed solution, stir, logical nitrogen 20 minutes, be warming up to 80～85 ℃, kept 15～20 minutes, and dripped monomer solution and initiator component that (1) step obtains continuously, dripped off in 3～6 hours, continue reaction 1～3 hour then, be cooled to 50 ℃ and add neutralizing agent accent pH value 8-9.
Chain-transfer agent can once add before reaction or add in reaction in batches.
Acrylic acid bulk hybridization emulsion of the present invention is used for frie retardant coating and protective system, but its erosion resistance application property, all can reach the state of the art of solvent-type acrylic coating with the sticking power of base material.And with the frie retardant coating and the protective system of this hybridisation emulsion preparation, the gloss of its water tolerance and coating and decorate properties are better than common water soluble acrylic acid coating greatly.So this emulsion is used for frie retardant coating, protective system and various building coating, not only have the good weathering resistance, anti-fouling performance of oiliness acrylic resin paint etc., be dispersion medium with water simultaneously also, satisfy environmental protection requirement.It is a kind of acrylic acid hybridisation emulsion with oiliness acrylic resin performance.The invention solves the contradiction that exists for a long time between coating property and the environmental requirement, energy-conservation, the Water-borne modification of paint industry, protection environment for human survival are had great significance.
Embodiment
The performance of the coating that further specifies the preparation method of acrylic acid bulk hybridization emulsion with embodiment below and obtain thus.
Embodiment 1
(1) monomer component: with the copolymer resins (molecular weight 40000) of 16g oiliness methyl methacrylate, 3g bisphenol A type epoxy resin (molecular weight 350～400), be dissolved in the mix monomer of 4g methacrylic acid, 25g butyl acrylate and 30g methyl methacrylate, and add the solubility promoter propylene glycol butyl ether 20g of increase system stability.
Initiator component: the 0.1g Potassium Persulphate is dissolved in the 20g deionized water.
(2) thermometer is being housed, agitator, in the four-hole bottle of reflux exchanger, add the 0.1g sodium bicarbonate, 0.5g Sodium dodecylbenzene sulfonate, 3g polyoxyethylene phenolic ether in ninth of the ten Heavenly Stems acrylate, the 10g polyoxyethylene nonylphenol ether is dissolved in the 120g deionized water, stir, logical nitrogen 20 minutes, add uncle's 0.5g 16 carbon mercaptan, the 1g methacrylic acid, the 1g Hydroxyethyl acrylate, the 8g butyl acrylate, the 10g methyl methacrylate, be warming up to 80 ℃ and add the 0.3g Potassium Persulphate, temperature keeps 81 ± 2 ℃ of reactions after 15 minutes, drips monomer component and initiator component in (1) simultaneously, drips in 3 hours, be warming up to 85 ℃ and continue reaction 1～2 hour, be cooled to 50 ℃ and transfer pH value with ammoniacal liquor.Can make solid content is 39.1%, and pH value is 8 hybridisation emulsion.
Embodiment 2
(1) monomer component: 10g oiliness methyl methacrylate copolymer resin, 10g oiliness butyl methacrylate and acrylonitrile compolymer resin, 3g Synolac, 0.2g benzoyl peroxide, 0.3 uncle's DDM dodecyl mercaptan are dissolved in the mix monomer of 4g vinylformic acid, 25g butyl acrylate and 30g vinyl cyanide, and add the solubility promoter propylene glycol monomethyl ether 18g of increase system stability.
Initiator component: the 0.1g ammonium persulphate is dissolved in the 20g deionized water.
(2) thermometer is being housed, agitator, in the four-hole bottle of reflux exchanger, add the 0.1g sodium bicarbonate, 0.5g sodium lauryl sulphate, the polycondensate of 3g Succinic Acid and glycidyl methacrylate, 5g alkylphenol polyoxyethylene, the 5g polyoxyethylene nonylphenol ether, be dissolved in the 120g deionized water, stir, logical nitrogen 20 minutes, add 0.2 uncle's DDM dodecyl mercaptan, 1g vinylformic acid, the 1g Propylene glycol monoacrylate, the 8g butyl acrylate, the 10g vinyl cyanide, be warming up to 80 ℃ and add the 0.3g ammonium persulphate, temperature keeps 81 ± 2 ℃, reacts after 15 minutes, drips monomer component and initiator component in (1) simultaneously, dripped in 3 hours, and be warming up to 85 ℃ and continue reaction 1～2 hour.Be cooled to 50 ℃, transfer pH value with Triethylene Diamine, can make solid content is 40.8%, the hybridisation emulsion of pH value 8.
Embodiment 3
(1) monomer component: with copolymer resins, 3g bisphenol A type epoxy resin (molecular weight 450～600) and the 0.2g Diisopropyl azodicarboxylate of 20g oiliness methyl methacrylate, be dissolved in the mix monomer of 4g methacrylic acid, 30g butyl acrylate and 40g methyl methacrylate, and add the solubility promoter 1-Methoxy-2-propyl acetate 20g of increase system stability.
Initiator component: the 0.15g ammonium persulphate is dissolved in the 20g deionized water.
(2) thermometer is housed, agitator, in the four-hole bottle of reflux exchanger, add the 0.1g sodium bicarbonate, 0.5g Sodium dodecylbenzene sulfonate, 3g polyoxyethylene phenolic ether in ninth of the ten Heavenly Stems acrylate, the 10g polyoxyethylene nonylphenol ether is dissolved in the 120g deionized water, stir, logical nitrogen 20 minutes adds 1g uncle ten carbon mercaptan, the 1g methacrylic acid, the 1g Hydroxyethyl acrylate, the 8g butyl acrylate, the 10g methyl methacrylate, be warming up to 80 ℃ and add the 0.3g ammonium persulphate, temperature keeps 81 ± 1 ℃ of reactions after 15 minutes, drips monomer component and initiator component in (1) simultaneously, drips in 3 hours, be warming up to 85 ℃, continue reaction 1～2 hour.Be cooled to 50 ℃, use N, the N dimethylethanolamine is transferred pH value, and can make solid content is 42.5%, and pH value is 8 emulsion.
Embodiment 4
(1) monomer component: with the homopolymerization resin of 8g oiliness methyl methacrylate, 8g methacrylic ester and cinnamic copolymer resins and 5g bisphenol A type epoxy resin (molecular weight 350～400), 0.2g Diisopropyl azodicarboxylate, be dissolved in the mix monomer of 2g methacrylic acid, 25g butyl acrylate and 30g vinyl cyanide, and add the solubility promoter propylene glycol butyl ether 20g of increase system stability.
Initiator component: the 0.1g Potassium Persulphate is dissolved in the 20g deionized water.
(2) thermometer is being housed, agitator, in the four-hole bottle of reflux exchanger, add the 0.1g sodium bicarbonate, the 1g disodium 4-dodecyl-2,4 '-oxydibenzenesulfonate, 10 polyoxyethylene phenolic ether in ninth of the ten Heavenly Stems acrylate are dissolved in the 120g deionized water, stir, logical nitrogen 20 minutes adds uncle's 0.5g 16 carbon mercaptan, the 1g methacrylic acid, the 1g Propylene glycol monoacrylate, the 8g butyl acrylate, the 10g vinyl cyanide is warming up to 80 ℃ and adds the 0.3g Potassium Persulphate, temperature keeps 81 ± 2 ℃ of reactions after 15 minutes, drip monomer component and initiator component in (1) simultaneously, dripped in 3 hours, be warming up to 85 ℃ and continue reaction 1～2 hour, be cooled to 50 ℃, transfer pH value with diethanolamine.Can make solid content is 39.1%, and pH value is 8 hybridisation emulsion.
Embodiment 5
(1) monomer component: with the copolymer resins of 15g oiliness methyl acrylate and 3g Synolac, 0.5 tert-dodecyl mercaptan, be dissolved in the mix monomer of 4g methacrylic acid, 20g butyl acrylate and 30g methyl methacrylate, and add the solubility promoter dipropylene glycol methyl ether 20g of increase system stability.
Initiator component: the 0.1g Potassium Persulphate is dissolved in the 20g deionized water.
(2) in the four-hole bottle that thermometer, agitator, reflux exchanger are housed, add the 0.1g sodium bicarbonate, 0.5g dodecyl biphenyl ether sulfonic acid sodium, 3g polyoxyethylene phenolic ether in ninth of the ten Heavenly Stems acrylate, 5g fat alkyd polyethenoxy ether sodium sulfate, the 5g polyoxyethylene nonylphenol ether is dissolved in the 120g deionized water, stirs, logical nitrogen 20 minutes; Add the 0.5g tert-dodecyl mercaptan, the 1g methacrylic acid, 1g Hydroxyethyl acrylate, 8g butyl acrylate, the 10g methyl methacrylate, be warming up to 80 ℃ and add the 0.2g ammonium persulphate, temperature keeps 81 ± 1 ℃ of reactions after 15 minutes, drips monomer component and initiator component in (1) simultaneously, dripped in 3 hours, and be warming up to 85 ℃ and continue reaction 1～2 hour.Be cooled to 50 ℃, use N, the N dimethylethanolamine is transferred pH value, and can make solid content is 38.8%, the hybridisation emulsion of pH value 9.
Embodiment 6
(1) monomer component: with the copolymer resins of 15g oiliness butyl acrylate, the copolymer resins of 5g oiliness methyl methacrylate (molecular weight 69000), 0.2g tertbutyl peroxide, be dissolved in the mix monomer of 3g vinylformic acid, 22g butyl methacrylate, 38g methyl acrylate, and add the solubility promoter of increase system stability: dipropylene glycol methyl ether 20g.
Initiator component: the 0.1g Potassium Persulphate is dissolved in the 20g deionized water.
(2) thermometer is being housed, agitator, in the four-hole bottle of reflux exchanger, add 0.1g yellow soda ash, 1.5g Sodium dodecylbenzene sulfonate, 3g polyoxyethylene phenolic ether in ninth of the ten Heavenly Stems acrylate, 5g polyoxyethylene nonylphenol ether and 2.3g sodium p styrene sulfonate are dissolved in the 100g deionized water, add the 3g n-methylolacrylamide again and be dissolved in 20g water, stir, logical nitrogen 20 minutes adds uncle's 0.5g 16 carbon mercaptan, 0.8g vinylformic acid, the 8g butyl methacrylate, the 11g methyl acrylate is warming up to 80 ℃, add the 0.3g Potassium Persulphate, temperature keeps 81 ± 2 ℃ of reactions after 15 minutes, drips monomer component and initiator component in (1) simultaneously, drips in 4 hours, be warming up to 85 ℃ and continue reaction 1～2 hour, be cooled to 50 ℃ and transfer pH value with trolamine.Can make solid content is 41%, and pH value is 8 hybridisation emulsion.
Embodiment 7
(1) monomer component: with 5g methacrylic ester and cinnamic copolymer resins, 5g acrylate and cinnamic copolymer resins, 5g methacrylic ester copolymer resins, the 5g Synolac, 0.2g benzoyl peroxide, be dissolved in the mix monomer of 3g vinylformic acid, 30g butyl acrylate and 25g Propenoic acid, 2-methyl, isobutyl ester, and add the solubility promoter propylene glycol butyl ether 20g of increase system stability.
Initiator component: the 0.1g Potassium Persulphate is dissolved in the 20g deionized water.
(2) thermometer is being housed, agitator, in the four-hole bottle of reflux exchanger, add the 0.1g sodium bicarbonate, 0.8g sodium laurylsulfonate, 3g acrylamide stearic acid sodium salt, 4g polyoxyethylene nonylphenol ether and 4g fat alkyd polyethenoxy ether sodium sulfate are dissolved in the 100g deionized water, stir, logical nitrogen 20 minutes adds the 3g diacetone-acryloamide(DAA) and is dissolved in 20g water, 1g vinylformic acid, the 10g butyl acrylate, the 10g Propenoic acid, 2-methyl, isobutyl ester, be warming up to 80 ℃ and add the 0.3g Potassium Persulphate, temperature keeps 81 ± 2 ℃, reacts after 15 minutes, drip monomer component and initiator component in (1) simultaneously, dripped in 3 hours, and be warming up to 85 ℃, continue reaction 1～2 hour, be cooled to 50 ℃, transfer pH value with ammoniacal liquor.Can make solid content is 39.1%, and pH value is 8 hybridisation emulsion.
Embodiment 8
(1) monomer component: with the copolymer resins of 12g oiliness methacrylic ester and vinyl cyanide, 8g bisphenol A type epoxy resin (molecular weight 400～650), be dissolved in the mix monomer of 4g vinylformic acid, 30g ethyl propenoate and 25g vinyl cyanide, and add the solubility promoter propylene glycol butyl ether 20g of increase system stability.
Initiator component: the 0.1g ammonium persulphate is dissolved in the 20g deionized water.
(2) thermometer is housed, agitator, in the four-hole bottle of reflux exchanger, add the 0.1g sodium bicarbonate, 1.5g sodium lauryl sulphate, 3g alkyl vinylformic acid-2-ethanesulfonic acid sodium, 6g base in ninth of the ten Heavenly Stems polyoxyethylene ether ammonium sulfate, be dissolved in the 120g deionized water, stir, logical nitrogen 20 minutes, add 0.5g uncle ten carbon mercaptan, 0.8g vinylformic acid, the 2g Hydroxyethyl acrylate, the 11g ethyl propenoate, the 8g vinyl cyanide, be warming up to 80 ℃ and add the 0.3g ammonium persulphate, temperature keeps 81 ± 2 ℃ of reactions after 15 minutes, drips monomer component and initiator component in (1) simultaneously, drips in 3 hours, be warming up to 85 ℃, continue reaction 1～2 hour, be cooled to 50 ℃, transfer pH value with Triethylene Diamine.Can make solid content is 39.1%, and pH value is 8 hybridisation emulsion.
Embodiment 9:
The prescription of the frie retardant coating that the hybridisation emulsion that adopts embodiment 2 to obtain prepares:
Ammonium polyphosphate 24.3g, melamine 7.8g, tetramethylolmethane 5.6g, dispersion agent 1.5g, defoamer 0.3g, hydroxylated cellulose 0.1g, film coalescence aid 1g, clorafin 4.2g, hybridisation emulsion 30g, deionized water 25.2g.
Embodiment 10:
The hybridisation emulsion that adopts embodiment 5 to obtain prepares the prescription of protective system:
Titanium dioxide 5.6g, ferric oxide 6.5g, talcum powder 11g, process white 8g, zinc phosphate 5.4g, dispersion agent 0.9g, defoamer 0.2g, thickening material 0.1g, inhibiter 2.6g, hybridisation emulsion 30g, deionized water 29.7g.
Claims (6)
1. acrylic acid bulk hybridization emulsion composition is characterized in that, by following material proportioning synthetic:
Parts by weight of raw materials
Acrylic monomer 20～40
Oiliness acrylic resin 5～20
Modified resin 1～5
Tensio-active agent 5～15
Initiator 0.1～0.3
Neutralizing agent 0.1～0.5
Deionized water 30～60
Chain-transfer agent 0.5～5
Solubility promoter 5～15
Described acrylic monomer comprise following one or more: vinylformic acid, methacrylic acid, methyl methacrylate, methyl acrylate, ethyl propenoate, Hydroxyethyl acrylate, Propylene glycol monoacrylate, butyl acrylate, butyl methacrylate, Propenoic acid, 2-methyl, isobutyl ester, ethyl acrylate;
Described oiliness acrylic resin is as hybrid resin, its molecular weight is between 40000～100000, the oiliness acrylic resin of second-order transition temperature between 30 ℃～60 ℃, be selected from following one or more: the copolymer resins of copolymer resins, methacrylic ester and the vinyl cyanide of the homopolymerization resin of acrylate, the homopolymerization resin of methacrylic ester, acrylate and cinnamic copolymer resins, methacrylic ester and cinnamic copolymer resins, acrylate and vinyl cyanide;
Described modified resin be selected from following one or more: urethane resin, Synolac, Resins, epoxy;
Described initiator comprises water soluble starter and oil-soluble initiator.
2. according to the acrylic acid bulk hybridization emulsion of claim 1, it is characterized in that, described tensio-active agent be selected from following one or more: sodium p styrene sulfonate, acrylamide stearic acid sodium salt, alkyl vinylformic acid-2-ethanesulfonic acid sodium salt, maleic acid higher alcohols monoester sodium salt, the polycondensate of Succinic Acid and glycidyl methacrylate, polyoxyethylene nonylphenol ether acrylate; Polyoxyethylene nonylphenol ether, polyoxyethylene octylphenol ether, polyoxyethylene lauric acid ester, polyoxyethylene stearic acid ester, Sodium dodecylbenzene sulfonate, Witco 1298 Soft Acid ammonium, disodium 4-dodecyl-2,4 '-oxydibenzenesulfonate, sodium lauryl sulphate, sodium laurylsulfonate, nonylphenol polyoxyethylene ether sulfate.
3. according to the acrylic acid bulk hybridization emulsion of claim 1, it is characterized in that, described water soluble starter be selected from following one or both: ammonium persulphate, Potassium Persulphate.
4. according to the acrylic acid bulk hybridization emulsion of claim 1, it is characterized in that, described oil-soluble initiator be selected from following one or both: benzoyl peroxide, Diisopropyl azodicarboxylate.
5. according to the acrylic acid bulk hybridization emulsion of claim 1, it is characterized in that, described solubility promoter be selected from following one or more: propylene glycol monomethyl ether, propylene glycol butyl ether, dipropylene glycol methyl ether, tripropylene glycol methyl ether, dipropylene glycol dme, 1-Methoxy-2-propyl acetate.
6. according to the acrylic acid bulk hybridization emulsion of claim 1, it is characterized in that, described chain-transfer agent be selected from following one or more: uncle's ten carbon mercaptan, uncle DDM dodecyl mercaptan, tert-dodecyl mercaptan, uncle's 16 carbon mercaptan, the hot carbon mercaptan of uncle.
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| CN101177468B (en) * | 2007-12-05 | 2012-07-04 | 东莞市英科水墨有限公司 | Water-soluble crylic acid resin and preparation method thereof |
| CN104449176B (en) * | 2013-02-07 | 2016-08-24 | 陈湘 | A kind of skin coating |
| CN104356840B (en) * | 2013-02-07 | 2017-02-08 | 河北晨阳工贸集团有限公司 | Coating for exterior walls of buildings |
| CN104341547B (en) * | 2013-07-29 | 2017-03-01 | 上海展辰涂料有限公司 | A kind of polyacrylate closing emulsion and preparation method thereof |
| CN103725068A (en) * | 2013-12-12 | 2014-04-16 | 青岛海洋新材料科技有限公司 | Aqueous antirust paint for ship cabin |
| CN105218725A (en) * | 2015-09-23 | 2016-01-06 | 南通瑞普埃尔生物工程有限公司 | A kind of preparation method of high adhesive force heavy-duty coating acrylate copolymer emulsion |
| CN105153828A (en) * | 2015-09-25 | 2015-12-16 | 南通瑞普埃尔生物工程有限公司 | Acrylic ester copolymer emulsion used for high-water-resistance heavy anti-corrosion coating and preparation method thereof |
| CN105153343A (en) * | 2015-09-29 | 2015-12-16 | 南通瑞普埃尔生物工程有限公司 | Acrylate copolymeric mini-emulsion for heavy anti-corrosion coating and preparation method of acrylate copolymeric mini-emulsion |
| CN106675291B (en) * | 2016-12-20 | 2018-11-02 | 浙江水马环保科技有限公司 | Polybasic ion antibacterial metal coating |
| CN109401746B (en) * | 2018-10-23 | 2021-05-14 | 中国石油化工股份有限公司 | Emulsion self-dispersion phase permeation regulator and preparation method thereof |
| CN111285953B (en) * | 2020-04-17 | 2023-02-03 | 株洲飞鹿高新材料技术股份有限公司 | Acrylic emulsion and preparation method thereof |
| CN116574520B (en) * | 2023-05-10 | 2024-03-22 | 湖南笙牛安全科技有限责任公司 | Fireproof gel and preparation method and application thereof |
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| CN1434063A (en) * | 2003-02-13 | 2003-08-06 | 海洋化工研究院 | Aqueous epoxy modified acrylic heat-reflecting thermo-insulating coating |
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| CN1434063A (en) * | 2003-02-13 | 2003-08-06 | 海洋化工研究院 | Aqueous epoxy modified acrylic heat-reflecting thermo-insulating coating |
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