WO2008133375A1 - Acrylic acid ester copolymer composition and redispersible powders - Google Patents

Acrylic acid ester copolymer composition and redispersible powders Download PDF

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Publication number
WO2008133375A1
WO2008133375A1 PCT/KR2007/004639 KR2007004639W WO2008133375A1 WO 2008133375 A1 WO2008133375 A1 WO 2008133375A1 KR 2007004639 W KR2007004639 W KR 2007004639W WO 2008133375 A1 WO2008133375 A1 WO 2008133375A1
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Prior art keywords
water
acrylic acid
soluble
acid ester
ester copolymer
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PCT/KR2007/004639
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French (fr)
Inventor
Jeong Woo Son
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Youngwoo Chemtech Co., Ltd.
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Application filed by Youngwoo Chemtech Co., Ltd. filed Critical Youngwoo Chemtech Co., Ltd.
Priority to US12/597,411 priority Critical patent/US20100160496A1/en
Priority to CN2007800429547A priority patent/CN101589104B/en
Priority to JP2010500809A priority patent/JP2010522798A/en
Priority to EP07833018A priority patent/EP2142597B1/en
Publication of WO2008133375A1 publication Critical patent/WO2008133375A1/en

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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • C08L33/04—Homopolymers or copolymers of esters
    • C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
    • C08L33/08—Homopolymers or copolymers of acrylic acid esters
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2/00—Processes of polymerisation
    • C08F2/12—Polymerisation in non-solvents
    • C08F2/16—Aqueous medium
    • C08F2/20—Aqueous medium with the aid of macromolecular dispersing agents
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10—Esters
    • C08F220/12—Esters of monohydric alcohols or phenols
    • C08F220/14—Methyl esters, e.g. methyl (meth)acrylate
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10—Esters
    • C08F220/12—Esters of monohydric alcohols or phenols
    • C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
    • C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10—Esters
    • C08F220/12—Esters of monohydric alcohols or phenols
    • C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
    • C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
    • C08F220/1804—C4-(meth)acrylate, e.g. butyl (meth)acrylate, isobutyl (meth)acrylate or tert-butyl (meth)acrylate
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L29/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical; Compositions of hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Compositions of derivatives of such polymers
    • C08L29/02—Homopolymers or copolymers of unsaturated alcohols
    • C08L29/04—Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L31/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid or of a haloformic acid; Compositions of derivatives of such polymers
    • C08L31/02—Homopolymers or copolymers of esters of monocarboxylic acids
    • C08L31/04—Homopolymers or copolymers of vinyl acetate
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • C08L33/02—Homopolymers or copolymers of acids; Metal or ammonium salts thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L39/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions of derivatives of such polymers
    • C08L39/04—Homopolymers or copolymers of monomers containing heterocyclic rings having nitrogen as ring member
    • C08L39/06—Homopolymers or copolymers of N-vinyl-pyrrolidones
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
    • C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
    • C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
    • C08L2666/04—Macromolecular compounds according to groups C08L7/00 - C08L49/00, or C08L55/00 - C08L57/00; Derivatives thereof

Definitions

  • the present invention relates to an acrylic acid ester copolymer composition, and redispersible powders made therefrom. More specifically, the present invention relates to an acrylic acid ester-based copolymer emulsion composition having excellent polymerization stability, and improved rater resistance, alkali resistance, and fluidity, and redispersible powders made from the composition.
  • emulsion polymerization is performed using monomers such as acrylic monomers and styrenic monomers
  • an anionic or nonionic surfactant is used as an emulsifier.
  • the emulsion prepared by using a surfactant has poor chemical stability when combined with an electrolyte, and as a result, if it is added to cement, or the like, there may be caused a problem that the fluidity of the cement composition is deteriorated.
  • polyvinyl alcohol could be used as a protective colloid.
  • the chemical stability was improved, but the polymerization stability was deteriorated, thereby still entailing a problem that a stable emulsion is hardly obtained.
  • a synthetic resin emulsion such as those of a vinyl acetate resin and an acrylic resin, has been widely used in the field such as an adhesive, a coating agent, and a cement additive.
  • This emulsion is typically supplied in a liquid form.
  • the liquid emulsion has a problem in that it requires high cost of transportation during the supply, and it can be frozen in the winter season, and as a result, its product quality varies over time.
  • the liquid emulsion is dried to form emulsion powders, which are used in various applications.
  • the synthetic resin emulsion powders should be redispersed in water for use, and accordingly, the powders are required to have excellent re ⁇ ispersibi J ity.
  • the present invention has been made to solve the afore-mentioned problems. It is an object of the present invention to provide an acrylic acid ester copolymer composition having excellent polymerization stability, and improved water resistance, alkali resistance, and fluidity, and redispersible powders made therefrom.
  • the acrylic acid ester copolymer emulsion composition according to one aspect of the present invention comprises polyvinyl alcohol (referred to as "PVA” hereinafter), hydrophilic ethylenic unsaturated monomers, hydrophobic ethylenic unsaturated monomers, and a lipophilic initiator.
  • PVA polyvinyl alcohol
  • the redispersible acrylic acid ester copolymer powders according to another aspect of the present invention are prepared by a spray-dry of the acrylic acid ester copolymer emulsion composition.
  • an inorganic hydraulic composition comprising redispersible acrylic acid ester copolymer powders, and an inorganic hydraulic material, wherein 1 to 30 parts by weight of the redispersible acrylic acid ester copolymer powders are preferably mixed with 100 parts by weight of the inorganic hydraulic material.
  • the acrylic acid ester emulsion copolymer composition, and the redispersible powders according to the present invention provide the effects as follows.
  • the acrylic acid ester copolymer composition prepared according to the present invention exhibits effects of yielding excellent polymerization stability, and improved water resistance, alkali resistance, and fluidity, and the redispersible powders prepared by a spray-dry of the acrylic acid ester copolymer composition has improved water redispersibiIity, and thus, can be used in various fields such as an additive to a hydraulic material, a powder paint, and an adhesive.
  • the acrylic acid ester copolymer emulsion composition according to the present invention comprises PVA having a degree of saponification of 85 mol% or more, and an average degree of polymerization of 300 to 1400, hydrophilic ethylenic unsaturated monomers having a water solubility of 1% or more, hydrophobic ethylenic unsaturated monomers having a water solubility of less than 1%, and a lipophilic initiator.
  • the acrylic acid ester copolymer emulsion composition comprises 4 to 15 parts by weight of PVA, and 0.01 to 1 part by weight of the lipophilic initiator, based on 100 parts by weight of the total monomers consisting of 20 to 70% by weight of the hydrophilic ethylenic unsaturated monomers, and 80 to 30% by weight of the hydrophobic ethylenic unsaturated monomers.
  • the total monomers mean the monomers consisting of the hydrophilic ethylenic unsaturated monomers and the hydrophobic ethylenic unsaturated monomers.
  • the PVA is a substance which is used as an emulsifier for emulsion polymerization, and the polymerization stability can be improved by using modified PVA, to which a functional group such as a mercapto group is introduced, in the emulsion polymerization.
  • modified PVA reduces the degree of polymerization, thereby leading to a problem that physical properties such as water resistance, mechanical strength, and durability are not assured. Thus, it is herein not recommended to use modified PVA.
  • PVA used as an emulsifier has a degree of saponification of 85 mol% or more, preferably 90 mol% or more. If PVA has a degree of saponification of less than 85 mol%, polymerization may not proceed stably, and thus, a good emulsion may not be formed.
  • PVA has an average degree of polymerization of 300 to 1400, preferably 300 to 600. If PVA has an average degree of polymerization of less than 300, the protective colloid ability of the particles may be insufficient, or polymerization may not proceed stably. If PVA has an average degree of polymerization of more than 1400, polymerization does not proceed stably due to the increased viscosity of the emulsion composition, and thus, a good emulsion cannot be formed.
  • PVA is used preferably in an amount of 4 to 15 parts by weight, more preferably in an amount of 6 to 9 parts by weight, based on 100 parts by weight of the total monomers contained in the emulsion composition. If the amount of PVA is less than 4 parts by weight, polymerization stability may be deteriorated, whereas if the amount of PVA is more than 15 parts by weight, polymerization may not proceed stably due to the increased viscosity.
  • the degree of saponification and the average degree of polymerization of PVA can be measured by commonly well-known methods, for example, in accordance with calculation methods as described in KS M 3013.
  • the hydrophilic ethylenic unsaturated monomers used in the emulsion composition of the present invention have a water solubility of 1.0% or more.
  • the hydrophilic ethylenic unsaturated monomers at least one selected from the group consisting of methyl (meth)acrylate, ethyl acrylate, dimethyl (ethyl)aminoethyl methacrylate, vinyl acetate, vinyl propionate, (meth)acrylonitrile, (meth)acrylamide, diacetone acrylamide, glycidyl methacrylate, 2-hydroxyethyl methacrylate, hydroxypropyl methacrylate, methoxyethyl (meth)acrylate, and ethoxyethyl (meth)aerylate can be used.
  • the hydrophilic ethylenic unsaturated monomers are used preferably in an amount of 20 to 70% by weight, more preferably in an amount of 40 to 60% by weight, based on 100 parts by weight of the total monomers contained in the emulsion composition.
  • the hydrophobic ethylenic unsaturated monomers used in the emulsion composition of the present invention have a water solubility of 1.0% or less.
  • the hydrophobic ethylenic unsaturated monomers at least one selected from the group consisting of n-butyl (meth)acrylate, i-butyl (meth)acrylate, t- butyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, stearyl (meth)acrylate, lauryl (meth)acrylate, tridecyl methacrylate, cyclohexyl methacrylate, acetoacetoxyethyl methacrylate, and styrene can be used.
  • the hydrophobic ethylenic unsaturated monomers are used preferably in an amount of 80 to 30% by weight, and preferably in an amount of 60 to 40% by weight, based on 100 parts by weight of the total monomers contained in the emulsion composition.
  • a lipophilic initiator is used as the initiator used in the emulsion composition of the present invention.
  • the lipophilic initiator at least one organic peroxide selected from the group consisting of benzoyl peroxide, lauryl peroxide, succinic peroxide, t-butyl peroxymaleic acid, t- butyl hydroperoxide, azobisdimethylvaleronitrile, and azoisobutyronitrile can be used.
  • succinic peroxide t-butyl peroxymaleic acid, or t-butyl hydroperoxide can be used.
  • the lipophilic initiator is used in an amount of 0.01 to 1 part by weight, preferably 0.05 to 0.5 part by weight, based on 100 parts by weight of the total monomers.
  • the acrylic acid ester copolymer emulsion composition according to the present invention can further comprise additional components, if desired.
  • additional components if desired.
  • a reducing agent, a polymerization controlling agent, a co-emulsifier, or the like can be selectively used, provided that it does not interfere with the properties of the emulsion composition.
  • the reducing agent can be used, if the temperature at which a radical generated from the organic peroxide as the lipophilic initiator has a half- life of 10 hours is higher than 90°C.
  • a reducing organic compound or a reducing inorganic compound can be used as the reducing agent.
  • the reducing agent if any, is used in an amount of 0.05 to 3 equivalents, preferably 0.5 to 2 equivalents, based on the amount of the polymerization initiator.
  • reducing organic compound at least one selected from the group consisting of L-ascorbic acid, tartaric acid, sodium organosulfinate, and formaldehyde sulfoxylate, metal salts, can be used.
  • reducing inorganic compound at least one selected from the group consisting of sodium sulfates, such as sodium thiosulfate, acidic sodium sulfite, and sodium metabisulfite, can be used.
  • a chain transfer agent As the polymerization controlling agent which is generally used in the emulsion polymerization, a chain transfer agent, a buffer, or the like can be used according to the purposes. However, if the chain transfer agent is used, the degree of polymerization of an acrylic polymer is reduced, and as a result, there is a problem that water resistance and durability among the technical properties of the obtained emulsion are decreased. Accordingly, it is preferable not to use a chain transfer agent in the acrylic acid ester copolymer emulsion composition of the present invention.
  • sodium acetate, sodium phosphate dibasic, or sodium sulfate, or a mixture of two or more kinds thereof can be used.
  • any one selected from an anionic, cationic, or nonionic surfactant, a water-soluble polymer having a protective colloid function, and a water-soluble oligomer can be used.
  • the co-emulsifier is used in a large amount, there is a problem that fusion and adhesion proceed while the emulsion composition is dried, thereby leading to reduced redispersibility.
  • a surfactant be not used as a co-emu!sifier in the acrylic acid ester copolymer emulsion composition of the present invention.
  • water-soluble polymer having a protective colloid function other than PVA examples include hydroxyethyl cellulose, polyvinyl pyrrolidone, methyl cellulose, and a starch derivative.
  • the water-soluble polymer modulates the viscosity when an emulsion composition is spray-dried into as an emulsion powder.
  • the redispersibility of the redispersible emulsion powder may be reduced.
  • the redispersible emulsion powders, if used, are preferably used within the range not interfering with the redispersibility of the redispersible emulsion powders.
  • the water-soluble oligomer may be a polymer or copolymer having a degree of polymerization of 10 to 500, which contains a hydrophilic group such as a sulfonate group, a carboxyl group, a hydroxyl group, and an alkyleneglycol group.
  • a hydrophilic group such as a sulfonate group, a carboxyl group, a hydroxyl group, and an alkyleneglycol group.
  • amide copolymers such as a 2-methacrylamide/2- methylpropanesulfonic acid copolymer, a sodium methacrylate/4- styrenesulfonate copolymer, a styrene/maleic acid copolymer, and ⁇ oly(meth)aerylate can be used.
  • a 2- methacrylamide/2-methylpropanesulfonic acid copolymer, or a sodium methacrylate/4-styrene-sulfonate copolymer is preferably used from .the viewpoint of redispersibility in water, and working stability with an inorganic hydraulic component.
  • the water-soluble oligomer which has been preliminarily polymerized before initiating the emulsion polymerization may be used.
  • the acrylic acid ester copolymer emulsion composition is a typical, uniform and milky white composition, and has an average particle diameter of 0.05 to 2.0 [M, preferably 0.5 to 1.0 ⁇ m.
  • the average particle diameter of the emulsion composition can be measured by a well-known method, for example, by using laser difiraction, and a scattering particle size distribution analyzer.
  • an additive may be added to the emulsion composition after emulsion polymerization, if desired.
  • the additive include an organic pigment, an inorganic pigment, a water-soluble additive, a pH modulator, a preservative, and an anti-oxidant .
  • the water-soluble additive can be added so as to improve the redispersibility of the powders obtained by a spray-dry of the emulsion composition, and the fluidity and adhesiveness of the redispersed emulsion.
  • the water-soluble additive if any, is added to the emulsion composition after emulsion polymerization and before drying.
  • the water-soluble additive is used preferably in an amount of 1 to 50 parts by weight, based on 100 parts by weight of the non-volatiles of the aqueous emulsion before drying. If the amount of the water-soluble additive is more than 50 parts by weight, the water resistance of the redispersible emulsion powder is insufficient, whereas if the amount of the water-soluble additive is less than 1 part by weight, improvement in redispersibility, fluidity, or adhesiveness may be insufficient.
  • the water-soluble additive at least one selected from the group consisting of polyvinyl alcohol (including cationic PVA), hydroxyethyl cellulose, methyl cellulose, a starch derivative (starch ether, including cationic starch), polyvinyl pyrrol idone, polyethylene oxide, a water-soluble alkyd resin, a water-soluble phenol resin, a water-soluble urea resin, a water-soluble melamine resin, a water-soluble guanamine resin, a water- soluble naphthalenesulfonic acid resin, a water-soluble amino resin, a water- soluble polyamide resin, a water-soluble acrylic resin, a water-soluble polycarboxylie acid resin, a water-soluble polyester resin, a water-soluble polyurethane resin, a water-soluble polyol resin, a water-soluble epoxy resin, and a cationizing agent can be used.
  • polyvinyl alcohol including cationic PVA
  • water-soluble additives PVA and a derivative thereof, and starch ether are effective for improving redispersibility, fluidity, and adhesiveness.
  • PYA used as the water-soluble additive may be the same or different compound from those used as an emulsifier in the polymerization process.
  • the acrylic acid ester copolymer emulsion composition according to the present invention is excellent in polymerization stability and mechanical stability, and as a result, it can be suitably used in various fields of a cement/mortar admixing agent, varnishes, construction materials, paints, adhesives, fiber and paper processing agents, and inorganic binders.
  • the term "redispersibility” means the property of powders to be redispersed in a water-based medium, such as water, to form an emulsion.
  • An anti-blocking agent can be used in combination, through mixing it with the emulsion powders produced after a spray-dry of, or through mixing it with the emulsion during a spray-dry of.
  • the anti-blocking agent generally well-known inactive, inorganic or organic powders, such as calcium carbonate, talc, clay, anhydrous silicic acid, aluminum silicate, white carbon, and alumina white, can be used.
  • anhydrous silicic acid, calcium carbonate, talc, or clay, each having an average particle diameter of 0.01 to 0.5 ⁇ m, are preferably used in combination.
  • the anti-blocking agent is used in an amount of 2 to 30% by weight, based on 100% by weight of the redispersible emulsion powders produced after a spray-dry of the composition.
  • the redispersible acrylic acid ester copolymer powders can be used in various fields such as an additive to a hydraulic material, a powder paint, and an adhesive, and preferably used as an additive to various hydraulic materials such as cement and gypsum.
  • the redispersible acrylic acid ester copolymer powders are mixed with an inorganic hydraulic material to produce an inorganic hydraulic composition.
  • the inorganic hydraulic material contained in the inorganic hydraulic composition at least one selected from various cement-based materials such as Portland cement, early strength cement, and rapid hardening cement, various gypsum-based materials such as inorganic gypsum, hemihydrate gypsum, and calcined gypsum, and blast furnace slag can be used.
  • various cement-based materials such as Portland cement, early strength cement, and rapid hardening cement
  • various gypsum-based materials such as inorganic gypsum, hemihydrate gypsum, and calcined gypsum, and blast furnace slag can be used.
  • the redispersible acrylic acid copolymer powders are preferably contained in an amount of 1 to 30 parts by weight, more preferably 5 to 20 parts by weight, based on 100 parts by weight of the inorganic hydraulic material. If the content of the redispersible acrylic acid copolymer powders is less than 1 part by weight, improvement in the adhesive power is insufficient, whereas if the content is more than 30 parts by weight, there is a problem that the hydraulic material doest not exhibit its ordinary performances.
  • the inorganic hydraulic composition can further comprise additional substances, and the additional substances can be selected from fly ash, limestone powders, calcium hydroxide, and calcium carbonate.
  • the acrylic acid ester copolymer emulsion composition according to the present invention can be prepared by performing emulsion polymerization under such a condition that facilitates graft polymerization to PVA having a degree of saponification of 85 mol% or more.
  • emulsion polymerization under such a condition that facilitates graft polymerization means that emulsion polymerization which is carried out using a lipophilic initiator at 20 to 90 °C.
  • Examples of the method for emulsion polymerization include a batch emulsion polymerization method comprising adding water, an emulsifier, monomers, and the like to a polymer at one, elevating the temperature of the mixture, • and adding an appropriate amount of a polymerization initiator thereto to perform polymerization; a monomer dropwise emulsion polymerization method comprising adding water and an emulsifier to a polymer, elevating the temperature of the mixture, and dropping monomers; and an emulsion monomer dropwise emulsion polymerization method comprising first emulsifying monomers using an emulsifier and water, and then dropping the emulsion, but the present invention is not limited to these emulsion polymerization methods.
  • the acrylic copolymer emulsion composition is prepared using a monomer dropwise emulsion polymerization method.
  • emulsion polymerization can be carried out by further using additional components such as a polymerization initiator, a polymerization controlling agent, and a co-emulsifier , if desired, in addition to the emulsifier and the monomer components, as described above.
  • additional components such as a polymerization initiator, a polymerization controlling agent, and a co-emulsifier , if desired, in addition to the emulsifier and the monomer components, as described above.
  • the redispersible powders can be prepared by drying the acrylic acid ester copolymer emulsion composition.
  • the drying method include a spray-dry of, freeze-drying, and hot air-drying.
  • a spray-dry of is preferably used from the viewpoint from re- emulsibility and productivity.
  • the spraying mode is not particularly limited, but spray can be performed using any of discs, nozzles, or the like, for example.
  • the heat source include hot air and hot steam.
  • the a spray-dry of temperature is preferably in the range of 70°C to 150°C .
  • the a spray-dry of treatment in the present invention involves modulating the content of the non-volatiles of the emulsion, continuously supplying the non-volatiles to a spray-drier, and drying the generated mist using hot air, thereby obtaining powders.
  • ⁇ 73> 130 parts by weight of water, 8 parts by weight of PVA having an average degree of polymerization of 500 and a degree of saponification of 98.0 to 99.0 mol% (Product Name: Polinol F05, manufactured by DC Chemical Co., Ltd., Korea), and 0.3 part by weight of sodium acetate as a buffer were fed into a reaction flask equipped with a stirrer, a thermometer, a condenser, and a dropping lot, and PVA was dissolved in water by heating the reaction flask to 80 ° C.
  • the monomer components 45 parts by weight of BA , 45 parts by weight of MMA, 0.4 part by weight of t-BPM as an initiator, and 0.4 part by weight L-ASA as a reducing agent were dropped into the reaction flask for about 4 hours to perform a dropwise polymerization reaction. After completion of dropping, the product was matured, and cooled to complete the reaction.
  • composition 1 aqueous acrylic copolymer emulsion composition having a solid content of about 45% by weight was obtained.
  • composition 2 An emulsion composition (Composition 2) was obtained in the same manner as in Example 1, except that the PVA was changed to a PVA having an average degree of polymerization of 500, and a degree of saponification of 85.5 to 87.5 mol% (Product Name: Polinol P05, manufactured by DC Chemical Co., Ltd., Korea) .
  • composition 3 An emulsion composition (Composition 3) was obtained in the same manner as in Example 1, except that the PVA was changed to a PVA having an average degree of polymerization of 1300, and a degree of saponification of 92.5 to 94.5 mol% (Product Name: PVA-613, manufactured by Kuraray Co., Ltd.), the initiator was changed to benzoyl peroxide (referred to as "BPO" hereinafter), no reducing agent was used, and the mixing ratio of BA ' ⁇ MMA was 4 : 6.
  • composition 4 An emulsion composition (Composition 4) was obtained in the same manner as in Example 1, except that the PVA was changed to a PVA having an average degree of polymerization of 1000, and a degree of saponification of 87.0 to 89.0 mol% (Product Name-' PVA-210, manufactured by Kuraray Co., Ltd.), the initiator was changed to t-butyl hydroperoxide (referred to as "t-BHP" hereinafter), no reducing agent was used, and the mixing ratio of BA : MMA is 6 : 4.
  • Emulsion polymerization was performed in the same manner as in the preparation method of Example 1, except that the PVA was changed to a PVA having an average degree of polymerization of 1700, and a degree of saponification of 94.5 to 95.5 mol% (Product Name: PVA-617, manufactured by Kuraray Co., Ltd.). However, the viscosity was increased during the polymerization, and as a result, a stable emulsion composition (Composition 5) could not obtained.
  • Emulsion polymerization was performed in the same manner as in the preparation method of Example 1, except that the PVA was changed to a PVA having an average degree of polymerization of 200, and a degree of saponification of 98.0 to 99.0 mol% (Product Name- PVA-102, manufactured by Kuraray Co., Ltd.). However, high viscosity was shown Cdilatancy' phenomenon) during the polymerization, and as a result, a stable emulsion composition (Composition 6) could not obtained.
  • Emulsion polymerization was performed in the same manner as in the preparation method of Example 1, except that the ratio of BA ' ⁇ MMA was changed to 90 : 10, the initiator was changed to BPO, and no reducing agent was used. However, a polymerization reaction did not proceed, and as a result, a stable emulsion composition (Composition 7) could not obtained.
  • Emulsion polymerization was performed in the same manner as in the preparation method of Example 1, except that the PVA was changed to a PVA having an average degree of polymerization of 500, and a degree of saponification of 85.5 to 87.5 mol% (Product Name: P05, manufactured by DC Chemical Co., Ltd., Korea), the initiator was changed to ammonium persulfate (referred to as "APS", hereinafter), and no reducing agent was used. However, a polymerization reaction did not proceed, and as a result, a stable emulsion composition (Composition 8) could not obtained.
  • APS ammonium persulfate
  • Emulsion powders were prepared in the same manner as described above, except that the emulsion composition 1 was changed to the emulsion compositions 2, 3, and 4.
  • TI Thixotropic Index Value
  • Test 3 Redispersiblilitv ⁇ i3o> 100 parts by weight of the prepared redispersible emulsion powders were mixed with 100 parts by weight of deionized water using a stirrer to obtain a redispersion. The redispersion was put into a glass tube, and left to stand at room temperature. The redispersion was evaluated using the following criteria ⁇
  • ⁇ i32> B State where the redispersion is separate into two phases, that is, a transparent liquid phase, and a precipitated emulsion powder phase;
  • test base plate 70X70X20 mm
  • KS F 4716 5.2
  • the sample was applied onto the test base plate for molding using a mold (40X40 mm), and cured in a curing chamber for 14 hours, thereby preparing a specimen.
  • Adhesion strength (N/mm 2 ) T/1600 ⁇ 142> wherein T is a maximum tensile load (N).

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Abstract

The present invention provides an acrylic acid ester copolymer emulsion composition, and redispersible powders made therefrom. The acrylic acid ester copolymer emulsion composition comprises polyvinyl alcohol having a degree of saponification of 85 mol% or more, and an average degree of polymerization of 300 to 1400; hydrophilic ethylenic unsaturated monomers having a water solubility of 1% or more; hydrophobic ethylenic unsaturated monomers having a water solubility of less than 1%; and a lipophilic initiator. The acrylic acid ester copolymer composition according to the present invention has excellent polymerization stability, and improved water resistance, alkali resistance, and fluidity, and the redispersible powders prepared by a spray-dry of the acrylic acid ester copolymer composition have improved water redispersibility, and thus, can be used in various fields such as an additive to a hydraulic material, a powder paint, and an adhesive.

Description

[DESCRIPTION] [Invention Title]
ACRYLIC ACID ESTER COPOLYMER COMPOSITION AND REDISPERSIBLE POWDERS [Technical Field]
<i> The present invention relates to an acrylic acid ester copolymer composition, and redispersible powders made therefrom. More specifically, the present invention relates to an acrylic acid ester-based copolymer emulsion composition having excellent polymerization stability, and improved rater resistance, alkali resistance, and fluidity, and redispersible powders made from the composition. [Background Art]
<2> Generally, when emulsion polymerization is performed using monomers such as acrylic monomers and styrenic monomers, an anionic or nonionic surfactant is used as an emulsifier. However, the emulsion prepared by using a surfactant has poor chemical stability when combined with an electrolyte, and as a result, if it is added to cement, or the like, there may be caused a problem that the fluidity of the cement composition is deteriorated.
<3> In order to overcome such problem associated with the use of the surfactant, polyvinyl alcohol could be used as a protective colloid. In this case, the chemical stability was improved, but the polymerization stability was deteriorated, thereby still entailing a problem that a stable emulsion is hardly obtained.
<4> Accordingly, there has been proposed a method involving using modified polyvinyl alcohol in which a functional group such as a mercapto group is introduced to one end, as a protective colloid, or a chain transfer agent in combination, to improve the polymerization stability. However, this method leads to a reduced degree of polymerization, and as a result, it cannot satisfy water resistance, mechanical strength, durability, or the like.
<5> On the other hand, a synthetic resin emulsion, such as those of a vinyl acetate resin and an acrylic resin, has been widely used in the field such as an adhesive, a coating agent, and a cement additive. <6> This emulsion is typically supplied in a liquid form. However, the liquid emulsion has a problem in that it requires high cost of transportation during the supply, and it can be frozen in the winter season, and as a result, its product quality varies over time.
<7> For the purpose of solving the problem as above, the liquid emulsion is dried to form emulsion powders, which are used in various applications. However, the synthetic resin emulsion powders should be redispersed in water for use, and accordingly, the powders are required to have excellent reόispersibi J ity. [Disclosure] [Technical Problem]
<s> Onόer these circumstances, the present invention has been made to solve the afore-mentioned problems. It is an object of the present invention to provide an acrylic acid ester copolymer composition having excellent polymerization stability, and improved water resistance, alkali resistance, and fluidity, and redispersible powders made therefrom.
<9> The other objects and advantages of the present invention will be further illustrated with reference to the following description, and be apparent from the following Examples, Further, the objects and advantages of the present invention can be realized using the means and combinations, as defined in the appended claims.
[Technical Solution]
<io> The acrylic acid ester copolymer emulsion composition according to one aspect of the present invention comprises polyvinyl alcohol (referred to as "PVA" hereinafter), hydrophilic ethylenic unsaturated monomers, hydrophobic ethylenic unsaturated monomers, and a lipophilic initiator.
<ii> The redispersible acrylic acid ester copolymer powders according to another aspect of the present invention are prepared by a spray-dry of the acrylic acid ester copolymer emulsion composition.
<i2> Further, there is provided an inorganic hydraulic composition comprising redispersible acrylic acid ester copolymer powders, and an inorganic hydraulic material, wherein 1 to 30 parts by weight of the redispersible acrylic acid ester copolymer powders are preferably mixed with 100 parts by weight of the inorganic hydraulic material. [Advantageous Effects]
<13> The acrylic acid ester emulsion copolymer composition, and the redispersible powders according to the present invention provide the effects as follows.
<14> The acrylic acid ester copolymer composition prepared according to the present invention exhibits effects of yielding excellent polymerization stability, and improved water resistance, alkali resistance, and fluidity, and the redispersible powders prepared by a spray-dry of the acrylic acid ester copolymer composition has improved water redispersibiIity, and thus, can be used in various fields such as an additive to a hydraulic material, a powder paint, and an adhesive. [Best Model
<i5> The terms and words which are used in the present specification and the appended claims should not be construed as being confined to common meanings or dictionary meanings but be construed as meanings and concepts matching with the technical spirit of the present invention based on the principle that an inventor can properly define the concept of a term to describe his/her invention in the best fashion.
<16> Therefore, Examples and constitutions as described herein do not cover all the technical spirit of the present invention but are merely the most preferred embodiments of the present invention. Thus, it should be understood that various equivalents and modifications can be made to the embodiments at the time of filing this application.
<i7> The acrylic acid ester copolymer emulsion composition according to the present invention comprises PVA having a degree of saponification of 85 mol% or more, and an average degree of polymerization of 300 to 1400, hydrophilic ethylenic unsaturated monomers having a water solubility of 1% or more, hydrophobic ethylenic unsaturated monomers having a water solubility of less than 1%, and a lipophilic initiator.
<18> The acrylic acid ester copolymer emulsion composition comprises 4 to 15 parts by weight of PVA, and 0.01 to 1 part by weight of the lipophilic initiator, based on 100 parts by weight of the total monomers consisting of 20 to 70% by weight of the hydrophilic ethylenic unsaturated monomers, and 80 to 30% by weight of the hydrophobic ethylenic unsaturated monomers.
<i9> As used herein, the total monomers mean the monomers consisting of the hydrophilic ethylenic unsaturated monomers and the hydrophobic ethylenic unsaturated monomers.
<20> The PVA is a substance which is used as an emulsifier for emulsion polymerization, and the polymerization stability can be improved by using modified PVA, to which a functional group such as a mercapto group is introduced, in the emulsion polymerization. However, the use of modified PVA reduces the degree of polymerization, thereby leading to a problem that physical properties such as water resistance, mechanical strength, and durability are not assured. Thus, it is herein not recommended to use modified PVA.
<2i> PVA used as an emulsifier has a degree of saponification of 85 mol% or more, preferably 90 mol% or more. If PVA has a degree of saponification of less than 85 mol%, polymerization may not proceed stably, and thus, a good emulsion may not be formed.
<22> Further, PVA has an average degree of polymerization of 300 to 1400, preferably 300 to 600. If PVA has an average degree of polymerization of less than 300, the protective colloid ability of the particles may be insufficient, or polymerization may not proceed stably. If PVA has an average degree of polymerization of more than 1400, polymerization does not proceed stably due to the increased viscosity of the emulsion composition, and thus, a good emulsion cannot be formed.
<23> PVA is used preferably in an amount of 4 to 15 parts by weight, more preferably in an amount of 6 to 9 parts by weight, based on 100 parts by weight of the total monomers contained in the emulsion composition. If the amount of PVA is less than 4 parts by weight, polymerization stability may be deteriorated, whereas if the amount of PVA is more than 15 parts by weight, polymerization may not proceed stably due to the increased viscosity.
<24> On the other hand, the degree of saponification and the average degree of polymerization of PVA can be measured by commonly well-known methods, for example, in accordance with calculation methods as described in KS M 3013.
<25> The hydrophilic ethylenic unsaturated monomers used in the emulsion composition of the present invention have a water solubility of 1.0% or more. As the hydrophilic ethylenic unsaturated monomers, at least one selected from the group consisting of methyl (meth)acrylate, ethyl acrylate, dimethyl (ethyl)aminoethyl methacrylate, vinyl acetate, vinyl propionate, (meth)acrylonitrile, (meth)acrylamide, diacetone acrylamide, glycidyl methacrylate, 2-hydroxyethyl methacrylate, hydroxypropyl methacrylate, methoxyethyl (meth)acrylate, and ethoxyethyl (meth)aerylate can be used.
<26> The hydrophilic ethylenic unsaturated monomers are used preferably in an amount of 20 to 70% by weight, more preferably in an amount of 40 to 60% by weight, based on 100 parts by weight of the total monomers contained in the emulsion composition.
<27> The hydrophobic ethylenic unsaturated monomers used in the emulsion composition of the present invention have a water solubility of 1.0% or less. As the hydrophobic ethylenic unsaturated monomers, at least one selected from the group consisting of n-butyl (meth)acrylate, i-butyl (meth)acrylate, t- butyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, stearyl (meth)acrylate, lauryl (meth)acrylate, tridecyl methacrylate, cyclohexyl methacrylate, acetoacetoxyethyl methacrylate, and styrene can be used.
<28> The hydrophobic ethylenic unsaturated monomers are used preferably in an amount of 80 to 30% by weight, and preferably in an amount of 60 to 40% by weight, based on 100 parts by weight of the total monomers contained in the emulsion composition.
<29> As the initiator used in the emulsion composition of the present invention, a lipophilic initiator is used. As the lipophilic initiator, at least one organic peroxide selected from the group consisting of benzoyl peroxide, lauryl peroxide, succinic peroxide, t-butyl peroxymaleic acid, t- butyl hydroperoxide, azobisdimethylvaleronitrile, and azoisobutyronitrile can be used.
<30> Preferably, from the viewpoint of convenience in use, succinic peroxide, t-butyl peroxymaleic acid, or t-butyl hydroperoxide can be used.
<3i> The lipophilic initiator is used in an amount of 0.01 to 1 part by weight, preferably 0.05 to 0.5 part by weight, based on 100 parts by weight of the total monomers.
<32> On the other hand, the acrylic acid ester copolymer emulsion composition according to the present invention can further comprise additional components, if desired. For example, a reducing agent, a polymerization controlling agent, a co-emulsifier, or the like can be selectively used, provided that it does not interfere with the properties of the emulsion composition.
<33> The reducing agent can be used, if the temperature at which a radical generated from the organic peroxide as the lipophilic initiator has a half- life of 10 hours is higher than 90°C. As the reducing agent, a reducing organic compound or a reducing inorganic compound can be used.
<34> The reducing agent, if any, is used in an amount of 0.05 to 3 equivalents, preferably 0.5 to 2 equivalents, based on the amount of the polymerization initiator.
<35> As the reducing organic compound, at least one selected from the group consisting of L-ascorbic acid, tartaric acid, sodium organosulfinate, and formaldehyde sulfoxylate, metal salts, can be used. As the reducing inorganic compound, at least one selected from the group consisting of sodium sulfates, such as sodium thiosulfate, acidic sodium sulfite, and sodium metabisulfite, can be used.
<36> As the polymerization controlling agent which is generally used in the emulsion polymerization, a chain transfer agent, a buffer, or the like can be used according to the purposes. However, if the chain transfer agent is used, the degree of polymerization of an acrylic polymer is reduced, and as a result, there is a problem that water resistance and durability among the technical properties of the obtained emulsion are decreased. Accordingly, it is preferable not to use a chain transfer agent in the acrylic acid ester copolymer emulsion composition of the present invention.
<37> As the buffer, sodium acetate, sodium phosphate dibasic, or sodium sulfate, or a mixture of two or more kinds thereof can be used.
<38> As the co-emulsifier which may be contained in the emulsion composition, any one selected from an anionic, cationic, or nonionic surfactant, a water-soluble polymer having a protective colloid function, and a water-soluble oligomer can be used. However, if the co-emulsifier is used in a large amount, there is a problem that fusion and adhesion proceed while the emulsion composition is dried, thereby leading to reduced redispersibility. For this reason, it is preferable that a surfactant be not used as a co-emu!sifier in the acrylic acid ester copolymer emulsion composition of the present invention.
<39> Examples of the water-soluble polymer having a protective colloid function other than PVA include hydroxyethyl cellulose, polyvinyl pyrrolidone, methyl cellulose, and a starch derivative. The water-soluble polymer modulates the viscosity when an emulsion composition is spray-dried into as an emulsion powder.
<40> However, depending on the amount of the water-soluble polymer to be used, the redispersibility of the redispersible emulsion powder may be reduced. Thus, the redispersible emulsion powders, if used, are preferably used within the range not interfering with the redispersibility of the redispersible emulsion powders.
<4i> The water-soluble oligomer may be a polymer or copolymer having a degree of polymerization of 10 to 500, which contains a hydrophilic group such as a sulfonate group, a carboxyl group, a hydroxyl group, and an alkyleneglycol group. As the water-soluble oligomer, at least one selected from the group consisting of amide copolymers such as a 2-methacrylamide/2- methylpropanesulfonic acid copolymer, a sodium methacrylate/4- styrenesulfonate copolymer, a styrene/maleic acid copolymer, and ρoly(meth)aerylate can be used.
<42> Among the afore-mentioned water-soluble oligomers, a 2- methacrylamide/2-methylpropanesulfonic acid copolymer, or a sodium methacrylate/4-styrene-sulfonate copolymer is preferably used from .the viewpoint of redispersibility in water, and working stability with an inorganic hydraulic component.
<43> Further, the water-soluble oligomer which has been preliminarily polymerized before initiating the emulsion polymerization may be used.
<44> The acrylic acid ester copolymer emulsion composition is a typical, uniform and milky white composition, and has an average particle diameter of 0.05 to 2.0 [M, preferably 0.5 to 1.0 μm. The average particle diameter of the emulsion composition can be measured by a well-known method, for example, by using laser difiraction, and a scattering particle size distribution analyzer.
<45> On the other hand, an additive may be added to the emulsion composition after emulsion polymerization, if desired. Examples of the additive include an organic pigment, an inorganic pigment, a water-soluble additive, a pH modulator, a preservative, and an anti-oxidant .
<46> The water-soluble additive can be added so as to improve the redispersibility of the powders obtained by a spray-dry of the emulsion composition, and the fluidity and adhesiveness of the redispersed emulsion. The water-soluble additive, if any, is added to the emulsion composition after emulsion polymerization and before drying.
<47> The water-soluble additive is used preferably in an amount of 1 to 50 parts by weight, based on 100 parts by weight of the non-volatiles of the aqueous emulsion before drying. If the amount of the water-soluble additive is more than 50 parts by weight, the water resistance of the redispersible emulsion powder is insufficient, whereas if the amount of the water-soluble additive is less than 1 part by weight, improvement in redispersibility, fluidity, or adhesiveness may be insufficient.
<48> As the water-soluble additive, at least one selected from the group consisting of polyvinyl alcohol (including cationic PVA), hydroxyethyl cellulose, methyl cellulose, a starch derivative (starch ether, including cationic starch), polyvinyl pyrrol idone, polyethylene oxide, a water-soluble alkyd resin, a water-soluble phenol resin, a water-soluble urea resin, a water-soluble melamine resin, a water-soluble guanamine resin, a water- soluble naphthalenesulfonic acid resin, a water-soluble amino resin, a water- soluble polyamide resin, a water-soluble acrylic resin, a water-soluble polycarboxylie acid resin, a water-soluble polyester resin, a water-soluble polyurethane resin, a water-soluble polyol resin, a water-soluble epoxy resin, and a cationizing agent can be used.
<49> Among the above-mentioned water-soluble additives, PVA and a derivative thereof, and starch ether are effective for improving redispersibility, fluidity, and adhesiveness. PYA used as the water-soluble additive may be the same or different compound from those used as an emulsifier in the polymerization process.
<50> The acrylic acid ester copolymer emulsion composition according to the present invention is excellent in polymerization stability and mechanical stability, and as a result, it can be suitably used in various fields of a cement/mortar admixing agent, varnishes, construction materials, paints, adhesives, fiber and paper processing agents, and inorganic binders.
<5i> On the other hand, there are provided redispersible acrylic acid ester copolymer powders prepared by a spray-dry of the acrylic acid ester copolymer emulsion composition.
<52> As used herein, the term "redispersibility" means the property of powders to be redispersed in a water-based medium, such as water, to form an emulsion.
<53> An anti-blocking agent can be used in combination, through mixing it with the emulsion powders produced after a spray-dry of, or through mixing it with the emulsion during a spray-dry of. <54> As the anti-blocking agent, generally well-known inactive, inorganic or organic powders, such as calcium carbonate, talc, clay, anhydrous silicic acid, aluminum silicate, white carbon, and alumina white, can be used. Among these, anhydrous silicic acid, calcium carbonate, talc, or clay, each having an average particle diameter of 0.01 to 0.5 μm, are preferably used in combination.
<55> The anti-blocking agent is used in an amount of 2 to 30% by weight, based on 100% by weight of the redispersible emulsion powders produced after a spray-dry of the composition.
<56> The redispersible acrylic acid ester copolymer powders can be used in various fields such as an additive to a hydraulic material, a powder paint, and an adhesive, and preferably used as an additive to various hydraulic materials such as cement and gypsum.
<57> The redispersible acrylic acid ester copolymer powders are mixed with an inorganic hydraulic material to produce an inorganic hydraulic composition.
<58> By adding the hydraulic material to the redispersible acrylic acid ester copolymer powders provided according to the present invention, there is obtained an advantage of improvement in the adhesive power under the wetting condition, as well as improvement in the adhesive power under an ordinary condition.
<59> As the inorganic hydraulic material contained in the inorganic hydraulic composition, at least one selected from various cement-based materials such as Portland cement, early strength cement, and rapid hardening cement, various gypsum-based materials such as inorganic gypsum, hemihydrate gypsum, and calcined gypsum, and blast furnace slag can be used.
<60> The redispersible acrylic acid copolymer powders are preferably contained in an amount of 1 to 30 parts by weight, more preferably 5 to 20 parts by weight, based on 100 parts by weight of the inorganic hydraulic material. If the content of the redispersible acrylic acid copolymer powders is less than 1 part by weight, improvement in the adhesive power is insufficient, whereas if the content is more than 30 parts by weight, there is a problem that the hydraulic material doest not exhibit its ordinary performances.
<6i> On the other hand, the inorganic hydraulic composition can further comprise additional substances, and the additional substances can be selected from fly ash, limestone powders, calcium hydroxide, and calcium carbonate.
<62> Hereinbelow, the methods for preparing the acrylic acid ester copolymer emulsion composition, and the redispersible powders made therefrom according to another aspect of the present invention will be described
<63> The acrylic acid ester copolymer emulsion composition according to the present invention can be prepared by performing emulsion polymerization under such a condition that facilitates graft polymerization to PVA having a degree of saponification of 85 mol% or more.
<64> As used herein, the expression "emulsion polymerization under such a condition that facilitates graft polymerization" means that emulsion polymerization which is carried out using a lipophilic initiator at 20 to 90 °C.
<65> Examples of the method for emulsion polymerization include a batch emulsion polymerization method comprising adding water, an emulsifier, monomers, and the like to a polymer at one, elevating the temperature of the mixture, • and adding an appropriate amount of a polymerization initiator thereto to perform polymerization; a monomer dropwise emulsion polymerization method comprising adding water and an emulsifier to a polymer, elevating the temperature of the mixture, and dropping monomers; and an emulsion monomer dropwise emulsion polymerization method comprising first emulsifying monomers using an emulsifier and water, and then dropping the emulsion, but the present invention is not limited to these emulsion polymerization methods. In the present invention, the acrylic copolymer emulsion composition is prepared using a monomer dropwise emulsion polymerization method.
<66> Generally, emulsion polymerization can be carried out by further using additional components such as a polymerization initiator, a polymerization controlling agent, and a co-emulsifier , if desired, in addition to the emulsifier and the monomer components, as described above.
<67> On the other hand, the redispersible powders can be prepared by drying the acrylic acid ester copolymer emulsion composition. Examples of the drying method include a spray-dry of, freeze-drying, and hot air-drying. Among these, a spray-dry of is preferably used from the viewpoint from re- emulsibility and productivity.
<68> In the case of a spray-dry of, the spraying mode is not particularly limited, but spray can be performed using any of discs, nozzles, or the like, for example. Examples of the heat source include hot air and hot steam. The a spray-dry of temperature is preferably in the range of 70°C to 150°C .
<69> Specifically, the a spray-dry of treatment in the present invention involves modulating the content of the non-volatiles of the emulsion, continuously supplying the non-volatiles to a spray-drier, and drying the generated mist using hot air, thereby obtaining powders.
<70> Hereinbelow, Examples of the present invention will be described in detai 1. [Mode for Invention]
<7i> Example 1
<72> Preparation of Acrylic Acid Ester Copolymer Emulsion Composition
<73> 130 parts by weight of water, 8 parts by weight of PVA having an average degree of polymerization of 500 and a degree of saponification of 98.0 to 99.0 mol% (Product Name: Polinol F05, manufactured by DC Chemical Co., Ltd., Korea), and 0.3 part by weight of sodium acetate as a buffer were fed into a reaction flask equipped with a stirrer, a thermometer, a condenser, and a dropping lot, and PVA was dissolved in water by heating the reaction flask to 80°C.
<74> Next, the temperature of the reaction flask was maintained at 80°C, 5 parts by weight of butyl acrylate (referred to as "BA" hereinafter) and 5 parts by weight of methyl metacrylate (referred to as "MMA" hereinafter) were added to the reaction flask, and then 0.1 part by weight of t-butyl peroxymaleic acid (referred to as "t-BPM" hereinafter) as a polymerization initiator, and 0.1 part by weight of L-ascorbic acid (referred to as 11L-ASA" hereinafter) as a reducing agent were further added into to the reaction flask, to perform a emulsion polymerization reaction for 1 hour.
<75> Further, the monomer components, 45 parts by weight of BA , 45 parts by weight of MMA, 0.4 part by weight of t-BPM as an initiator, and 0.4 part by weight L-ASA as a reducing agent were dropped into the reaction flask for about 4 hours to perform a dropwise polymerization reaction. After completion of dropping, the product was matured, and cooled to complete the reaction.
<76> By using such preparation method, an aqueous acrylic copolymer emulsion composition (Composition 1) having a solid content of about 45% by weight was obtained.
<77>
<78> Example 2
<79> An emulsion composition (Composition 2) was obtained in the same manner as in Example 1, except that the PVA was changed to a PVA having an average degree of polymerization of 500, and a degree of saponification of 85.5 to 87.5 mol% (Product Name: Polinol P05, manufactured by DC Chemical Co., Ltd., Korea) .
<80>
<8i> Example 3
<82> An emulsion composition (Composition 3) was obtained in the same manner as in Example 1, except that the PVA was changed to a PVA having an average degree of polymerization of 1300, and a degree of saponification of 92.5 to 94.5 mol% (Product Name: PVA-613, manufactured by Kuraray Co., Ltd.), the initiator was changed to benzoyl peroxide (referred to as "BPO" hereinafter), no reducing agent was used, and the mixing ratio of BA '■ MMA was 4 : 6.
<83> On the other hand, during the emulsion reaction, BA and MMA were added to the reaction flask in the amounts of 4 parts by weight and 6 parts by weight, respectively, and during the dropwise polymerization reaction, BA and MMA were fed to the reaction flask in the amounts of 36 parts by weight and 54 parts by weight, respectively.
<84>
<85> Example 4
<86> An emulsion composition (Composition 4) was obtained in the same manner as in Example 1, except that the PVA was changed to a PVA having an average degree of polymerization of 1000, and a degree of saponification of 87.0 to 89.0 mol% (Product Name-' PVA-210, manufactured by Kuraray Co., Ltd.), the initiator was changed to t-butyl hydroperoxide (referred to as "t-BHP" hereinafter), no reducing agent was used, and the mixing ratio of BA : MMA is 6 : 4.
<87> On the other hand, during the emulsion reaction, BA and MMA were added in the amounts of 6 parts by weight and 4 parts by weight, respectively, to the reaction flask, and during the dropwise polymerization reaction, BA and MMA were fed in the amounts of 54 parts by weight and 36 parts by weight, respectively, to the reaction flask.
<88>
<89> Comparative Example 1
<90> Emulsion polymerization was performed in the same manner as in the preparation method of Example 1, except that the PVA was changed to a PVA having an average degree of polymerization of 1700, and a degree of saponification of 94.5 to 95.5 mol% (Product Name: PVA-617, manufactured by Kuraray Co., Ltd.). However, the viscosity was increased during the polymerization, and as a result, a stable emulsion composition (Composition 5) could not obtained.
<91>
<92> Comparative Example 2
<93> Emulsion polymerization was performed in the same manner as in the preparation method of Example 1, except that the PVA was changed to a PVA having an average degree of polymerization of 200, and a degree of saponification of 98.0 to 99.0 mol% (Product Name- PVA-102, manufactured by Kuraray Co., Ltd.). However, high viscosity was shown Cdilatancy' phenomenon) during the polymerization, and as a result, a stable emulsion composition (Composition 6) could not obtained.
<94>
<95> Comparative Example 3
<96> Emulsion polymerization was performed in the same manner as in the preparation method of Example 1, except that the ratio of BA '■ MMA was changed to 90 : 10, the initiator was changed to BPO, and no reducing agent was used. However, a polymerization reaction did not proceed, and as a result, a stable emulsion composition (Composition 7) could not obtained.
<97>
<98> Comparative Example 4
<99> Emulsion polymerization was performed in the same manner as in the preparation method of Example 1, except that the PVA was changed to a PVA having an average degree of polymerization of 500, and a degree of saponification of 85.5 to 87.5 mol% (Product Name: P05, manufactured by DC Chemical Co., Ltd., Korea), the initiator was changed to ammonium persulfate (referred to as "APS", hereinafter), and no reducing agent was used. However, a polymerization reaction did not proceed, and as a result, a stable emulsion composition (Composition 8) could not obtained.
<ioo> The specifications of Examples and Comparative Examples are summarized in Table 1 below.
<101>
<i02> [Table 1] <103> <10S>
<110> <111> <112> <113>
Figure imgf000017_0001
<114> In Examples and Comparative Examples, PVA, the initiator, and the reducing agent were added in the amounts of 8 parts by weight, 0.5 part by weight, and 0.5 part by weight, respectively, based on 100 parts by weight of the total monomers.
<115> <116> Preparation of Redispersible Acrylic Acid Ester Copolymer Emulsion
Powders
<117> To 100 parts by weight of the emulsion composition 1, 50 parts by weight of a 20 wt% solution of PVA (Product Name: P05, manufactured by DC Chemical Co., Ltd., Korea) as a water-soluble additive was added, and the mixture was spray-dried in the presence of 15 parts by weight of an anti¬ blocking agent (SE-SUPER manufactured by NAINTSCH, dolomite talc) to obtain emulsion powders.
<ii8> Emulsion powders were prepared in the same manner as described above, except that the emulsion composition 1 was changed to the emulsion compositions 2, 3, and 4.
<ii9> On the other hand, an emulsion composition could not be obtained from Compositions 5 to 8, and as a result, redispersible powders could not be also prepared therefrom.
<120>
<i2i> Evaluation test>
<122> Test l: Polymerization Stability
<123> Whether each of the emulsion compositions was gelled during the polymerization was confirmed. If the emulsion composition was not gelled, the produced emulsion was filtered through a 200-mesh Pylen sieve (ASTM standard sieve). After filtration, the weight of the filtrate was measured. The contents of the residues (rag/100 g EM) per 100 g of the solid content of the emulsion are shown in Table 2. If the content of the residue after filtration was 30 mg or less, the polymerization stability was evaluated to be excellent.
<124>
<125> Test 2: Fluidity
<i26> TI (Thixotropic Index Value) was calculated by measuring the viscosities at 6 rpm and 60 rpm of each of the emulsion compositions using a Brookfield-type viscometer. If the TI was 2.5 or less, the fluidity was evaluated to be excellent.
<127> n at 6 rpm/ iχ at 60 rpm = TI
<128>
<129> Test 3: Redispersiblilitv <i3o> 100 parts by weight of the prepared redispersible emulsion powders were mixed with 100 parts by weight of deionized water using a stirrer to obtain a redispersion. The redispersion was put into a glass tube, and left to stand at room temperature. The redispersion was evaluated using the following criteria^
<i3i> A: State where a uniform redispersion was obtained, and precipitation of the emulsion powders was not substantially observed;
<i32> B: State where the redispersion is separate into two phases, that is, a transparent liquid phase, and a precipitated emulsion powder phase; and
<133> - : State where no emulsion powder is prepared.
<134>
<i35> Test 4'- Test on water resistant adhesion strength of cement mortar
<i36> Cement materials with a ratio of Portland cement: standard sand = 1 : 3, and the redispersible emulsion powders obtained in Examples 1 to 4 were blended at a ratio of 10 ■' 1, and the blend was further added with water to adjust a flow value to be 170±5.
<i37> Next, the surface of a mortar substrate (70X70X20 mm) was abraded with an abrasive paper of KS Regulation No. 150. Each specimen was formed on this substrate using a mold, and the obtained specimen was immersed in water for 24 hours. Then, the adhesion strength was measured in the wet state using a universal test machine (manufactured by Shimadzu Corporation).
<i38> Cement materials with a ratio of Portland cement: standard sand = 1 : 3, and the redispersible emulsion powders obtained in Examples 1 to 4 were blended at a ratio of 10 : 1, and the blend was further blended with water to adjust a flow value to be 170+5, thereby preparing a sample.
<i39> Next, a test base plate (70X70X20 mm) was prepared in accordance with KS F 4716 (5.2), and the sample was applied onto the test base plate for molding using a mold (40X40 mm), and cured in a curing chamber for 14 hours, thereby preparing a specimen.
<14O> The cured specimen was placed horizontally in the curing chamber, and an adhesive was applied onto the surface of the sample. Then, an upper tensile zig was adhered thereto, left to stand for 24 hours, and immersed in water again for 24 hours. The adhesion strength was measured in the wet state, and a maximum tensile load was determined by applying a tensile force vertically onto the surface of the sample using a tensile test machine. The adhesion strength was calculated using the following equation, and expressed to one digit after decimal point.
<141> Adhesion strength (N/mm2) = T/1600 <142> wherein T is a maximum tensile load (N).
2 <143> If the adhesion strength was measured to be 1.0 N/mm or more, it was evaluated to be good. The results are shown in Table 2.
<144> <145> [Table 2} <146> <147>
<1SΘ> <151>
Figure imgf000020_0001
<152> Various Examples as described above are provided by way of illustration of the present invention only, and should not be construed to limit the present invention. Those skilled in the art will readily recognize various modifications and changes which may be made to the present invention, without departing from the spirit and scope of the present invention and the eQiiivalents defined by the appended claims.

Claims
[CLAIMS] [Claim 1]
<i54> An acrylic acid ester copolymer emulsion composition comprising:
<155> polyvinyl alcohol (PVA) having a degree of saponification of 85 mol% or more, and an average degree of polymerization of 300 to 1400;
<i56> hydrophilic ethylenic unsaturated monomers having a water solubility of 1% or more;
<157> hydrophobic ethylenic unsaturated monomers having a water solubility of less than 1%; and
<i58> a lipophilic initiator. [Claim 21
<i59> The acrylic acid ester copolymer emulsion composition according to claim 1, wherein the acrylic acid copolymer ester emulsion composition comprises 4 to 15 parts by weight of PVA, and the lipophilic initiator, based on 100 parts by weight of the total monomers consisting of 20 to 70% by weight of the hydrophilic ethylenic unsaturated monomers, and 80 to 30% by weight of the hydrophobic ethylenic unsaturated monomers.
[Claim 3]
<i60> The acrylic acid ester copolymer emulsion composition according to claim 1 or 2, wherein said lipophilic initiator is at least one organic peroxide selected from the group consisting of benzoyl peroxide, lauryl peroxide, succinic peroxide, t-butyl peroxymaleic acid, t-butyl hydroperoxide, azobisdimethylvaleronitrile, and azoisobutyronitrile.
[Claim 4]
<i6i> The acrylic acid ester copolymer emulsion composition according to claim 1 or 2, wherein said hydrophilic ethylenic unsaturated monomers are at least one selected from the group consisting of methyl (meth)acrylate, ethyl acrylate, dimethyl (ethyl)ami-noethyl methacrylate, vinyl acetate, vinyl propionate, (meth)acrylonitrile, (meth)aery1amide, diacetone acrylamide, glycidyl methacrylate, 2-hydroxyethyl methacrylate, hydroxypropyl methacrylate, methoxyethyl (meth)acrylate, and ethoxyethyl (meth)acrylate.
[Claim 5]
<162> The acrylic acid ester copolymer emulsion composition according to claim 1 or 2, wherein said hydrophobic ethylenic unsaturated monomers are at least one selected from the group consisting of n-butyl (meth)acrylate, i- butyl (meth)acrylate, t-butyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, stearyl (meth)acrylate, lauryl (meth)acrylate, tridecyl methacrylate, cyclohexyl methacrylate, acetoacetoxyethyl methacrylate, and styrene.
[Claim 6]
<163> The acrylic acid ester copolymer emulsion composition according to claim 1 or 2, wherein the acrylic acid ester copolymer emulsion composition further comprises a water-soluble additive.
[Claim 7]
<i64> The acrylic acid ester copolymer emulsion composition according to claim 6, wherein said water-soluble additive is at least one selected from the group consisting of polyvinyl alcohol, hydroxyethyl cellulose, methyl cellulose, a starch derivative, polyvinyl pyrrol idone, polyethylene oxide, a water-soluble alkyd resin, a water-soluble phenol resin, a water-soluble urea resin, a water-soluble melamine resin, a water-soluble guanamine resin, a water-soluble naphthalenesulfonic acid resin, a water-soluble amino resin, a water-soluble polyamide resin, a water-soluble acrylic resin, a water-soluble polycarboxylic acid resin, a water-soluble polyester resin, a water-soluble polyurethane resin, a water-soluble polyol resin, a water-soluble epoxy resin, and a cationizing agent, and is added in an amount of 1 to 50 parts by weight, based on 100 parts by weight of the non-volatiles of the emulsion composition.
[Claim 8]
<165> Redispersible acrylic acid ester copolymer powders prepared by a spray- dry of the acrylic acid ester copolymer emulsion composition according to any one of claims 1, 2 and 6.
[Claim 9]
<166> An inorganic hydraulic composition comprising the redispersible acrylic acid ester copolymer powders according to claim 8, and an inorganic hydraulic material .
[Claim 10] The inorganic hydraulic composition according to claim 9, wherein the inorganic hydraulic material is at least one selected from cement-based materials, gypsum-based materials, and blast furnace slag.
PCT/KR2007/004639 2007-04-27 2007-09-21 Acrylic acid ester copolymer composition and redispersible powders WO2008133375A1 (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2433984A1 (en) 2010-09-27 2012-03-28 Dow Global Technologies LLC Styrene-butadiene based redispersible polymer powders with improved stability in cement applications
CN110724416A (en) * 2019-09-25 2020-01-24 湖北工业大学 Preparation method of modified hydroxyl ester-based polymer emulsion

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5718074B2 (en) * 2011-01-20 2015-05-13 日本合成化学工業株式会社 POLYMER CEMENT COMPOSITION, COATING WATERPROOF MATERIAL USING SAME, AND EMULSION COMPOSITION FOR POLYMER CEMENT
CN102757196B (en) * 2012-07-25 2013-09-11 天津市南开区房地产管理局 Waterproof cement additive and cement containing same
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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0925381A (en) * 1995-07-11 1997-01-28 Kuraray Co Ltd Aqueous emulsion and flame-retardant coating material
WO1999016794A1 (en) * 1997-09-26 1999-04-08 Wacker-Chemie Gmbh Method for producing polymers stabilised with protective colloids
JP2001072705A (en) * 1999-06-29 2001-03-21 Honen Corp Vinyl acetate/(meth)acrylate copolymer, preparation thereof, and adhesive composition using it
WO2005108519A1 (en) * 2004-05-07 2005-11-17 Asahi Kasei Chemicals Corporation Aqueous resin dispersion for adhesive and composition thereof
JP2006028381A (en) * 2004-07-20 2006-02-02 Denki Kagaku Kogyo Kk Method for producing acrylic emulsion and acrylic emulsion

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4838789B1 (en) * 1970-07-31 1973-11-20
JPS5324106B2 (en) * 1974-05-25 1978-07-19
CA2110448A1 (en) * 1992-12-08 1994-06-09 Helen H.Y. Pak-Harvey Redispersible acrylic polymer powder for cementitious compositions
DE19502435A1 (en) * 1995-01-26 1996-08-01 Elotex Ag Chemical composition containing a) a copolymer based on styrene and / or alkyl (meth) acrylate and at least one further comonomer and b) a protective colloid, its aqueous polymer dispersion, process for its preparation and its use
US5563187A (en) * 1995-02-16 1996-10-08 Rohm And Haas Company Grafted polymer composition
US5741871A (en) * 1996-06-14 1998-04-21 Air Products And Chemicals, Inc. Acrylic emulsions prepared in the presence of fully hydrolyzed poly (vinyl alcohol)
US5753036A (en) * 1997-04-21 1998-05-19 Air Products And Chemicals, Inc. Poly(vinyl alcohol) stabilized acrylic polymer modified hydraulic cement systems
JP4099862B2 (en) * 1998-05-28 2008-06-11 日本ゼオン株式会社 Aqueous emulsion and method for producing the same
DE19901307C1 (en) * 1999-01-15 2000-06-21 Clariant Gmbh Powder dispersion, for mortar modification and adhesive for heat insulation systems, contains partially acetylated water soluble polyvinyl alcohol
DE19928933A1 (en) * 1999-06-24 2000-12-28 Wacker Polymer Systems Gmbh Process for the production of polyvinyl alcohol-stabilized polymers
DE19962566A1 (en) * 1999-12-23 2001-07-05 Wacker Polymer Systems Gmbh Process for the production of vinyl ester (meth) acrylic acid ester copolymers
DE10035587A1 (en) * 2000-07-21 2002-02-07 Wacker Polymer Systems Gmbh Process for the production of protective colloid-stabilized polymers by means of continuous emulsion polymerization
JP2002167403A (en) * 2000-09-19 2002-06-11 Kuraray Co Ltd Method for producing vinylester resin emulsion
US6593412B1 (en) * 2000-09-27 2003-07-15 Air Products Polymers, L.P. Water based emulsion copolymers incorporating vinyl ethylene carbonate
DE10126560C1 (en) * 2001-05-31 2002-09-12 Wacker Polymer Systems Gmbh Use of stabilized copolymers of vinyl ester, (meth)acrylate ester and optionally ethylene in building materials involves making the copolymers by radical emulsion polymerisation in two stages in presence of protective colloid
JP5142430B2 (en) * 2001-06-26 2013-02-13 日本合成化学工業株式会社 Redispersible synthetic resin powder and use thereof
DE10253046A1 (en) * 2002-11-14 2004-06-03 Wacker Polymer Systems Gmbh & Co. Kg Protective colloid-stabilized polymers in the form of their aqueous dispersions and water-redispersible powders

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0925381A (en) * 1995-07-11 1997-01-28 Kuraray Co Ltd Aqueous emulsion and flame-retardant coating material
WO1999016794A1 (en) * 1997-09-26 1999-04-08 Wacker-Chemie Gmbh Method for producing polymers stabilised with protective colloids
JP2001072705A (en) * 1999-06-29 2001-03-21 Honen Corp Vinyl acetate/(meth)acrylate copolymer, preparation thereof, and adhesive composition using it
WO2005108519A1 (en) * 2004-05-07 2005-11-17 Asahi Kasei Chemicals Corporation Aqueous resin dispersion for adhesive and composition thereof
JP2006028381A (en) * 2004-07-20 2006-02-02 Denki Kagaku Kogyo Kk Method for producing acrylic emulsion and acrylic emulsion

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP2142597A4 *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2433984A1 (en) 2010-09-27 2012-03-28 Dow Global Technologies LLC Styrene-butadiene based redispersible polymer powders with improved stability in cement applications
US9199881B2 (en) 2010-09-27 2015-12-01 Dow Global Technologies, Llc Styrene-butadiene based redispersible polymer powders with improved stability in cement applications
CN110724416A (en) * 2019-09-25 2020-01-24 湖北工业大学 Preparation method of modified hydroxyl ester-based polymer emulsion

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