WO2017073443A1 - 中空重合体粒子の水性分散液の製造方法、紙塗工用組成物および塗工紙 - Google Patents
中空重合体粒子の水性分散液の製造方法、紙塗工用組成物および塗工紙 Download PDFInfo
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- WO2017073443A1 WO2017073443A1 PCT/JP2016/081066 JP2016081066W WO2017073443A1 WO 2017073443 A1 WO2017073443 A1 WO 2017073443A1 JP 2016081066 W JP2016081066 W JP 2016081066W WO 2017073443 A1 WO2017073443 A1 WO 2017073443A1
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- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 1
- PRKQVKDSMLBJBJ-UHFFFAOYSA-N ammonium carbonate Chemical class N.N.OC(O)=O PRKQVKDSMLBJBJ-UHFFFAOYSA-N 0.000 description 1
- 235000012501 ammonium carbonate Nutrition 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- 229920005601 base polymer Polymers 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical class C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- UTOVMEACOLCUCK-PLNGDYQASA-N butyl maleate Chemical compound CCCCOC(=O)\C=C/C(O)=O UTOVMEACOLCUCK-PLNGDYQASA-N 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 229930016911 cinnamic acid Natural products 0.000 description 1
- 235000013985 cinnamic acid Nutrition 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- SPTHWAJJMLCAQF-UHFFFAOYSA-M ctk4f8481 Chemical compound [O-]O.CC(C)C1=CC=CC=C1C(C)C SPTHWAJJMLCAQF-UHFFFAOYSA-M 0.000 description 1
- VTXVGVNLYGSIAR-UHFFFAOYSA-N decane-1-thiol Chemical compound CCCCCCCCCCS VTXVGVNLYGSIAR-UHFFFAOYSA-N 0.000 description 1
- PGAXJQVAHDTGBB-UHFFFAOYSA-N dibutylcarbamothioylsulfanyl n,n-dibutylcarbamodithioate Chemical compound CCCCN(CCCC)C(=S)SSC(=S)N(CCCC)CCCC PGAXJQVAHDTGBB-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000004815 dispersion polymer Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 150000002019 disulfides Chemical class 0.000 description 1
- 229960002377 dixanthogen Drugs 0.000 description 1
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 238000010556 emulsion polymerization method Methods 0.000 description 1
- BEGBSFPALGFMJI-UHFFFAOYSA-N ethene;sodium Chemical group [Na].C=C BEGBSFPALGFMJI-UHFFFAOYSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- ORTRWBYBJVGVQC-UHFFFAOYSA-N hexadecane-1-thiol Chemical compound CCCCCCCCCCCCCCCCS ORTRWBYBJVGVQC-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 229920001477 hydrophilic polymer Polymers 0.000 description 1
- NXPHCVPFHOVZBC-UHFFFAOYSA-N hydroxylamine;sulfuric acid Chemical compound ON.OS(O)(=O)=O NXPHCVPFHOVZBC-UHFFFAOYSA-N 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 150000002500 ions Chemical group 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- ZWWQICJTBOCQLA-UHFFFAOYSA-N o-propan-2-yl (propan-2-yloxycarbothioyldisulfanyl)methanethioate Chemical compound CC(C)OC(=S)SSC(=S)OC(C)C ZWWQICJTBOCQLA-UHFFFAOYSA-N 0.000 description 1
- KZCOBXFFBQJQHH-UHFFFAOYSA-N octane-1-thiol Chemical compound CCCCCCCCS KZCOBXFFBQJQHH-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 229940096992 potassium oleate Drugs 0.000 description 1
- 229940114930 potassium stearate Drugs 0.000 description 1
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
- 235000011151 potassium sulphates Nutrition 0.000 description 1
- MLICVSDCCDDWMD-KVVVOXFISA-M potassium;(z)-octadec-9-enoate Chemical compound [K+].CCCCCCCC\C=C/CCCCCCCC([O-])=O MLICVSDCCDDWMD-KVVVOXFISA-M 0.000 description 1
- ANBFRLKBEIFNQU-UHFFFAOYSA-M potassium;octadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCCCC([O-])=O ANBFRLKBEIFNQU-UHFFFAOYSA-M 0.000 description 1
- FZYCEURIEDTWNS-UHFFFAOYSA-N prop-1-en-2-ylbenzene Chemical compound CC(=C)C1=CC=CC=C1.CC(=C)C1=CC=CC=C1 FZYCEURIEDTWNS-UHFFFAOYSA-N 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 235000011008 sodium phosphates Nutrition 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical group C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000002345 surface coating layer Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- YKFLAYDHMOASIY-UHFFFAOYSA-N γ-terpinene Chemical compound CC(C)C1=CCC(C)=CC1 YKFLAYDHMOASIY-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
- D21H21/50—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by form
- D21H21/52—Additives of definite length or shape
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
- D21H21/50—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by form
- D21H21/52—Additives of definite length or shape
- D21H21/54—Additives of definite length or shape being spherical, e.g. microcapsules, beads
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J13/00—Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
- B01J13/02—Making microcapsules or microballoons
- B01J13/06—Making microcapsules or microballoons by phase separation
- B01J13/14—Polymerisation; cross-linking
- B01J13/18—In situ polymerisation with all reactants being present in the same phase
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J13/00—Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
- B01J13/02—Making microcapsules or microballoons
- B01J13/20—After-treatment of capsule walls, e.g. hardening
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J13/00—Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
- B01J13/02—Making microcapsules or microballoons
- B01J13/20—After-treatment of capsule walls, e.g. hardening
- B01J13/22—Coating
-
- 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
- C08F2/22—Emulsion polymerisation
-
- 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
- C08F2/44—Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers
-
- 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
- C08F265/00—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00
- C08F265/04—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00 on to polymers of 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
- C08F265/00—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00
- C08F265/04—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00 on to polymers of esters
- C08F265/06—Polymerisation of acrylate or methacrylate esters on to polymers thereof
-
- 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
- C08F285/00—Macromolecular compounds obtained by polymerising monomers on to preformed graft polymers
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/35—Polyalkenes, e.g. polystyrene
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/37—Polymers of unsaturated acids or derivatives thereof, e.g. polyacrylates
- D21H17/375—Poly(meth)acrylamide
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/10—Coatings without pigments
- D21H19/14—Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12
- D21H19/20—Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12 comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
- D21H19/38—Coatings with pigments characterised by the pigments
- D21H19/42—Coatings with pigments characterised by the pigments at least partly organic
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
- D21H19/44—Coatings with pigments characterised by the other ingredients, e.g. the binder or dispersing agent
- D21H19/56—Macromolecular organic compounds or oligomers thereof obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H19/58—Polymers or oligomers of diolefins, aromatic vinyl monomers or unsaturated acids or derivatives thereof
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
- D21H21/14—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
- D21H21/28—Colorants ; Pigments or opacifying agents
Definitions
- the present invention relates to a method for producing an aqueous dispersion of hollow polymer particles, a composition for paper coating, and coated paper.
- Hollow polymer particles scatter light better and lower light transmission than polymer particles in which the polymer is densely and uniformly packed in the particles, and from the ease of deformation of the particles,
- an organic pigment excellent in optical properties such as a masking agent, opacity, whiteness, and glossiness, it is widely used in applications such as water-based paints and paper coating compositions.
- the void ratio of the hollow polymer particles to be blended is improved in order to improve the effects of reducing the weight of paints, coated papers, etc. and heat insulation, opacification and high gloss by the hollow polymer particles. It is desired to increase it and to improve various characteristics.
- a coating composition containing hollow polymer particles has been used as a paper coating composition in the production of coated paper.
- Patent Document 1 in order to obtain an aqueous dispersion of hollow polymer particles with little aggregate, polymer particles having a four-layer structure of a core polymer particle, an inner shell layer, an intermediate shell layer, and an outer shell layer are used.
- a base By adding a base to the aqueous dispersion containing the pH to be 7 or more, a part of the acidic groups contained in the core polymer particles is neutralized to form voids inside the core polymer particles.
- a method for obtaining an aqueous dispersion of hollow polymer particles is disclosed.
- Patent Documents 2 and 3 describe the presence of unreacted monomers that lead the shell layer after the shell layer is formed on the core polymer particle.
- a method for obtaining an aqueous dispersion of hollow polymer particles by finally adding a base, swelling the core polymer particles, and further polymerizing unreacted monomers to form a shell layer is disclosed.
- the hollow polymer particles are used as an organic pigment for paper coating, it is required not only to increase the porosity but also to improve the white paper gloss, but the coated paper coated with the aqueous dispersion liquid is required. The white paper gloss was not high enough.
- An object of the present invention is to provide a method for producing an aqueous dispersion of hollow polymer particles, which can obtain hollow polymer particles having a high porosity and further having sufficient white paper gloss when used in the production of coated paper. Furthermore, it is to provide a paper coating composition and coated paper using the hollow polymer particles.
- the present inventors have made the core polymer particles (A) substantially swell in the presence of a predetermined amount of monomer by swelling the core polymer particles (A) with a predetermined amount of base.
- the above-mentioned problems can be solved by swelling the first shell layer (B) that surrounds the target and making the difference in moisture content before and after swelling the first shell layer (B) a predetermined range.
- the invention has been completed.
- the monomers contained in the monomer mixture (a) and the monomer mixture (b) In the aqueous dispersion containing the core polymer particles (A) on which the first shell layer (B) is formed, the monomers contained in the monomer mixture (a) and the monomer mixture (b)
- the core swelling step of adding 0.1 to 30 parts by weight with respect to 100 parts by weight of the total amount to swell the core polymer particles (A), and the monomer mixture (c) are combined with the first shell layer (B )
- the hollow polymer according to (1) comprising a second shell layer forming step of copolymerizing in the presence of an aqueous dispersion containing the formed core polymer particles (A) to form a second shell layer (C)
- a method for producing an aqueous dispersion of particles (3)
- the monomer mixture (b1) is copolymerized in the presence of the core polymer particle (A) to substantially surround the core polymer particle (A).
- the monomer mixture (a) contains 20 to 50% by weight of an acid group-containing monomer and 50 to 80% by weight of a monomer copolymerizable therewith, and the monomer mixture (b1 ) Contains 1 to 10% by weight of an acidic group-containing monomer and 90 to 99% by weight of a monomer copolymerizable therewith, and the monomer mixture (b2) 2 to 2.5% by weight, and 97.5 to 99.8% by weight of a monomer copolymerizable therewith, and the monomer mixture (b3) is an acid group-containing monomer 0 to 0 .
- the method for producing an aqueous dispersion of hollow polymer particles according to (3) which comprises 15% by weight and 99.85 to 100% by weight of a monomer other than the acidic group-containing monomer, (5)
- the ratio of the monomer mixture (a), the monomer mixture (b1), the monomer mixture (b2), and the monomer mixture (b3) is expressed as “monomer mixture (a)”.
- a hollow polymer particle having a high porosity and a sufficient white paper gloss when used in the production of coated paper the hollow polymer particle A paper coating composition and coated paper using can be obtained.
- the method for producing an aqueous dispersion of hollow polymer particles according to the present invention comprises a step of copolymerizing the monomer mixture (a) to form core polymer particles (A), and a monomer mixture (b).
- the first shell layer forming step and the base are added to the aqueous dispersion containing the core polymer particles (A) on which the first shell layer (B) has been formed, to the monomer mixture (a) and the simple substance.
- the mixture (c) is added to an aqueous dispersion containing the core polymer particles (A) on which the first shell layer (B) is formed.
- 0.1 to 45 parts by weight is added to 100 parts by weight of the total amount of monomers contained in the monomer mixture (a) and the monomer mixture (b), and the first shell layer (B) is added.
- the water content difference represented by the water content of the core polymer particles (A) on which the shell layer (B) is formed is 1 to 45%.
- the monomer mixture (a) is copolymerized to form the core polymer particles (A).
- the monomer to be contained in the monomer mixture (a) for forming the core polymer particles (A) is not particularly limited, but the acidic group-containing monomer is 20 to 50% by weight, and the acidic group-containing single amount. Those containing 50 to 80% by weight of a monomer copolymerizable with the polymer are preferred.
- the acidic group-containing monomer is a monomer having a functional group showing acidity, for example, ethylenically unsaturated monocarboxylic acid such as acrylic acid, methacrylic acid, crotonic acid, cinnamic acid; itaconic acid, fumaric acid Ethylenically unsaturated polycarboxylic acids such as maleic acid and butenetricarboxylic acid; partially esterified products of ethylenically unsaturated polyvalent carboxylic acids such as monobutyl fumarate and monobutyl maleate; sulfonic acid group-containing monoesters such as styrenesulfonic acid And the like.
- ethylenically unsaturated monocarboxylic acid such as acrylic acid, methacrylic acid, crotonic acid, cinnamic acid
- itaconic acid fumaric acid
- Ethylenically unsaturated polycarboxylic acids such as maleic acid and butenetric
- the ethylenically unsaturated monocarboxylic acid monomer is preferable because the effect of the present invention becomes more remarkable, and represents (meth) acrylic acid (“acrylic acid and methacrylic acid”. The same applies hereinafter. ) Is more preferable, and methacrylic acid is particularly preferable. These monomers may be used alone or in combination of two or more.
- the content ratio of the acidic group-containing monomer in the monomer mixture (a) is preferably 20 to 50% by weight, more preferably 25 to 45% by weight.
- the content ratio of the acidic group-containing monomer is within the above range, so that the core polymer particles (A) are swollen by the base in the core swelling step described later. And the formation of voids becomes difficult, and the content ratio of the acidic group-containing monomer is too large, so that the core polymer particles (A) are sufficiently formed in the first shell. It is not surrounded by the layer (B), and the phenomenon that the stability of the aqueous dispersion is lowered in the core swelling step and aggregates are easily generated can be suppressed.
- the copolymerizable monomer is not particularly limited as long as it is a monomer copolymerizable with an acidic group-containing monomer, and includes styrene, ⁇ -methylstyrene, p-methylstyrene, halogenated styrene, and the like.
- Aromatic ethyl monomers such as acrylonitrile and methacrylonitrile; methyl (meth) acrylate, ethyl (meth) acrylate, butyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, Ethylenically unsaturated carboxylic acid ester monomers such as lauryl (meth) acrylate, glycidyl (meth) acrylate, 2-hydroxyethyl (meth) acrylate; (meth) acrylamide, N-methylol (meth) acrylamide, N-butoxymethyl (Meth) acrylamide and other ethylenically unsaturated compounds Boronamide monomers; Conjugated diene monomers such as butadiene and isoprene; Carboxylic acid vinyl ester monomers such as vinyl acetate; Vinyl halide monomers such as vinyl chloride; Vinylidene halides such as vinylidene chloride Vinyl pyr
- the carbon number of the alkyl group of the ethylenically unsaturated monocarboxylic acid alkyl ester monomer is preferably 1-6. These monomers may be used alone or in combination of two or more.
- the content ratio of the copolymerizable monomer in the monomer mixture (a) is preferably 50 to 80% by weight, more preferably 55 to 75% by weight.
- methyl methacrylate is 45 to 65% by weight
- butyl acrylate is 5 to 12% by weight
- methacrylic acid is 30 to 43% by weight.
- a crosslinkable monomer such as divinylbenzene, diallyl phthalate, allyl (meth) acrylate, or ethylene glycol di (meth) acrylate may be blended.
- the amount of the crosslinkable monomer used in the monomer mixture (a) is desirably within a range in which stable void formation can be maintained, preferably 20% by weight or less, more preferably 10% by weight or less, particularly preferably. Is 1% by weight or less.
- the use amount of the crosslinkable monomer is within the above range, the use amount of the crosslinkable monomer is too large, so that the core polymer particles (A) are hardly swollen by the base, and it is difficult to form voids. Can be suppressed.
- the copolymerization of the monomer mixture (a) is usually performed in an aqueous medium. Therefore, the core polymer particles (A) obtained by copolymerization are usually obtained in the state of an aqueous dispersion.
- the aqueous medium water is usually used, and a water-soluble organic solvent such as methanol and ethanol may be used in combination as long as the dispersion stability of the polymer particles during production is not impaired.
- the amount of the aqueous medium used is usually 100 to 1000 parts by weight, preferably 200 to 600 parts by weight, per 100 parts by weight of the monomer mixture (a).
- the amount of aqueous medium used is within the above range, the amount of aggregates generated during polymerization can be suppressed because the amount of aqueous medium used is too small, and the amount of aqueous medium used is also reduced. Therefore, the phenomenon that the productivity of the hollow polymer particles is inferior can be suppressed.
- the copolymerization method of the monomer mixture (a) is not particularly limited, but is usually an emulsion polymerization method.
- the polymerization method may be any of batch, semi-continuous and continuous methods.
- the polymerization pressure, polymerization temperature, and polymerization time are not particularly limited, and known conditions are employed.
- various additives such as surfactants, polymerization initiators, chain transfer agents, chelating agents, electrolytes, oxygen scavengers and the like that are commonly used in emulsion polymerization reactions may be used as polymerization auxiliary materials. it can.
- surfactant used in the emulsion polymerization generally known surfactants can be used. Specifically, rosinates such as potassium rosinate and sodium rosinate; potassium oleate, potassium laurate, lauric acid Anionic surfactants such as sodium fatty acid salts such as sodium, sodium stearate, potassium stearate; sulfates of fatty alcohols such as sodium lauryl sulfate; alkylaryl sulfonic acids such as sodium dodecylbenzenesulfonate; polyoxyethylene Alkyl ether sulfate such as sodium alkyl ether sulfate; nonionic surfactant such as alkyl ester of polyethylene glycol, alkyl ether or alkyl phenyl ether, polyacrylic acid, polymethacrylic acid, polyvinyl sulfonic acid Dispersion stabilizers such as hydrophilic synthetic polymer materials such as polyvinyl alcohol, polyvinyl pyrrolidone
- the amount of the surfactant used is preferably 0.1 to 5 parts by weight, more preferably 0.5 to 3 parts by weight with respect to 100 parts by weight of the monomer mixture (a).
- the amount of the surfactant used is in the above range, so that the phenomenon that aggregates are likely to be generated during polymerization can be suppressed. Since the amount is too large, it is possible to suppress the phenomenon that the void ratio of the obtained hollow polymer particles is lowered and various properties are deteriorated.
- the copolymerization of the monomer mixture (a) is preferably carried out in the presence of a seed.
- the particle diameter of the core polymer particles (A) to be produced can be easily controlled. can do.
- the polymerization conversion rate of the monomer mixture (a) in emulsion polymerization is usually 90% by weight or more, preferably 97% by weight or more.
- the composition of the copolymer to be produced is usually substantially the same as the composition of the monomer mixture (a).
- the method for adding the surfactant during the emulsion polymerization is not particularly limited, and the surfactant can be added to the reaction system all at once, in a divided manner or continuously.
- the method of continuously adding to the reaction system is preferable from the viewpoint of suppressing the generation of aggregates.
- the monomer mixture (a) and the surfactant may be mixed and added to the reaction system, or may be added separately to the reaction system, but the monomer mixture (a) It is preferable to mix the surfactant and the surfactant together with the aqueous medium and add them to the reaction system as an emulsion.
- an inorganic salt may be added to the reaction system and copolymerization may be performed in the presence of the inorganic salt.
- a surfactant and an inorganic salt are used in combination, the formation of aggregates during the polymerization Can be effectively suppressed, and the particle size distribution can be narrowed.
- an inorganic salt Specifically, it is alkali such as sodium chloride, potassium chloride, sodium sulfate, potassium sulfate, sodium nitrate, sodium carbonate, sodium hydrogen carbonate, potassium carbonate, sodium phosphate, sodium tripolyphosphate.
- the amount of the inorganic salt used is preferably 0.01 to 1 part by weight, more preferably 0.05 to 0.5 part by weight with respect to 100 parts by weight of the monomer mixture (a). If the amount of the inorganic salt used is in the above range, the amount of the inorganic salt used is too small, so that the phenomenon that the effect of addition is difficult to be exhibited can be suppressed, and the amount of the inorganic salt used is too large. Therefore, it is possible to suppress the phenomenon that aggregates are easily generated during polymerization. Moreover, it does not specifically limit as an addition method of an inorganic salt, It can add to a reaction system collectively, divided
- the volume average particle diameter of the core polymer particles (A) obtained by emulsion polymerization is preferably 100 to 600 nm, more preferably 250 to 500 nm.
- the volume average particle diameter is in the above range, the volume average particle diameter is too small, and therefore, it is possible to suppress the phenomenon that it becomes difficult to produce hollow polymer particles having a high porosity and a large particle diameter, Since the volume average particle diameter is too large, it becomes difficult to coat the core polymer particles (A) with the first shell layer (B), and it becomes difficult to form voids in the core polymer particles (A). Can be suppressed.
- first shell layer forming step In the first shell layer forming step of the present invention, the monomer mixture (b) is copolymerized in the presence of the core polymer particles (A) to substantially surround the core polymer particles (A). Then, the first shell layer (B) that is not swollen with respect to the base is formed.
- non-swelling with respect to the base means that the moisture content of the shell layer does not change before and after the addition of the base.
- the monomer mixture constituting the shell layer is copolymerized to produce dense polymer particles. Do.
- the first shell layer (B) may be a single layer or may be formed of two or more layers.
- the number of layers forming the first shell layer (B) is not particularly limited.
- the first shell layer (B) includes an inner shell layer (B1), an intermediate shell layer (B2), and an outer shell layer (B3). A shell layer formed of three layers can be employed.
- the first shell layer (B) formed from such three layers is obtained by copolymerizing the monomer mixture (b1) in the presence of the core polymer particle (A), thereby obtaining the core polymer particle (A).
- Inner shell layer forming step In the inner shell layer forming step, the monomer mixture (b1) is copolymerized in the presence of the core polymer particles (A), and the core polymer particles (A) are substantially An enclosing inner shell layer (B1) is formed.
- the monomer to be contained in the monomer mixture (b1) for forming the inner shell layer (B1) is not particularly limited, but the acidic group-containing monomer is 1 to 10% by weight, and the acidic group-containing monomer. Those containing 90 to 99% by weight of a monomer copolymerizable with the polymer.
- the acidic group-containing monomer is not particularly limited and may be the same as the core polymer particle (A) described above, but an ethylenically unsaturated monocarboxylic acid monomer is preferable, and (meth) Acrylic acid is more preferred, and methacrylic acid is particularly preferred.
- the content ratio of the acidic group-containing monomer in the monomer mixture (b1) is preferably 1 to 10% by weight, more preferably 3 to 9% by weight, and further preferably 5 to 8% by weight. It is.
- the copolymerizable monomer is not particularly limited, and the same copolymer as the above-described core polymer particle (A) can be used.
- an ethylenically unsaturated carboxylic acid ester monomer is used.
- an ethylenically unsaturated monocarboxylic acid alkyl ester monomer is more preferable, methyl (meth) acrylate and butyl (meth) acrylate are further preferable, and methyl methacrylate and butyl acrylate are particularly preferable.
- the carbon number of the alkyl group of the ethylenically unsaturated monocarboxylic acid alkyl ester monomer is preferably 1-6. These monomers may be used alone or in combination of two or more.
- the content of the copolymerizable monomer in the monomer mixture (b1) is preferably 90 to 99% by weight, more preferably 91 to 97% by weight, still more preferably 92 to 95% by weight. is there.
- methyl methacrylate, butyl acrylate, and methacrylic acid and / or acrylic acid in combination as each monomer constituting the monomer mixture (b1).
- the proportion is preferably 68 to 89% by weight of methyl methacrylate, 10 to 22% by weight of butyl acrylate, 1 to 10% by weight of methacrylic acid and / or acrylic acid, 71 to 85% by weight of methyl methacrylate, and 12 to 20% of butyl acrylate.
- methacrylic acid and / or acrylic acid More preferably, it is 3% to 9% by weight of methacrylic acid and / or acrylic acid, 74 to 81% by weight of methyl methacrylate, 14 to 18% by weight of butyl acrylate, 5 to 8% by weight of methacrylic acid and / or acrylic acid. It is particularly preferable that
- the method of copolymerizing the monomer mixture (b1) in the presence of the core polymer particles (A) is not particularly limited, but the monomer mixture in the aqueous dispersion of the core polymer particles (A) is not limited.
- a method of emulsion polymerization of (b1) is preferred, whereby the core polymer particles (A) on which the inner shell layer (B1) is formed can be obtained.
- the polymerization method any of batch method, semi-continuous method and continuous method may be used, and the polymerization pressure, polymerization temperature and polymerization time are not particularly limited, and known conditions can be adopted.
- the polymerization auxiliary materials exemplified in the production of the core polymer particles (A) can be used.
- a chain transfer agent may be used in addition to the polymerization auxiliary material exemplified in the production of the core polymer particles (A).
- the chain transfer agent known chain transfer agents used in general emulsion polymerization can be used.
- octyl mercaptan, n-dodecyl mercaptan, t-dodecyl mercaptan, n-hexadecyl mercaptan, n-tetra Mercaptans such as decyl mercaptan and t-tetradecyl mercaptan
- xanthogen disulfides such as dimethylxanthogen disulfide, diethylxanthogen disulfide and diisopropylxanthogen disulfide
- thiuram disulfides such as tetramethylthiuram disulfide, tetraethylthiuram disulfide and tetrabutylthiuram disulfide
- Halogenated hydrocarbons such as carbon chloride and carbon tetrabromide
- diphenylethylene, pentaphenylethane, ⁇ -methylstyrene dimer Hydrocarbons such
- chain transfer agents can be used alone or in combination of two or more.
- mercaptans and ⁇ -methylstyrene dimer are preferable, mercaptans are more preferable, and t-dodecyl mercaptan is particularly preferable.
- the monomer mixture (b2) is copolymerized in the presence of the core polymer particles (A) on which the inner shell layer (B1) is formed, and the inner shell layer ( An intermediate shell layer (B2) that substantially surrounds B1) is formed.
- the monomer to be contained in the monomer mixture (b2) for forming the intermediate shell layer (B2) is not particularly limited, but the acidic group-containing monomer is 0.2 to 2.5% by weight, and the acidic group Those containing 97.5 to 99.8% by weight of monomers copolymerizable with the containing monomer are preferred.
- the acidic group-containing monomer is not particularly limited and may be the same as the core polymer particle (A) described above, but an ethylenically unsaturated monocarboxylic acid monomer is preferable, and (meth) Acrylic acid is more preferred.
- the content ratio of the acidic group-containing monomer in the monomer mixture (b2) is preferably 0.2 to 2.5% by weight, more preferably 0.3 to 2.2% by weight, More preferably, it is 0.4 to 1.8% by weight.
- the copolymerizable monomer is not particularly limited, and the same copolymer as the above-described core polymer particle (A) can be used.
- aromatic vinyl monomers and ethylenically unsaturated monomers can be used.
- Monocarboxylic acid ester monomers are preferred, aromatic vinyl monomers are more preferred, and styrene is particularly preferred.
- the content of the copolymerizable monomer in the monomer mixture (b2) is preferably 97.5 to 99.8% by weight, more preferably 97.8 to 99.7% by weight, Preferably, it is 98.2 to 99.6% by weight.
- a combination of methacrylic acid and / or acrylic acid and styrene is particularly preferable to use a combination of methacrylic acid and / or acrylic acid and styrene as each monomer constituting the monomer mixture (b2).
- / or acrylic acid is preferably 0.2 to 2.5% by weight and styrene 97.5 to 99.8% by weight, methacrylic acid and / or acrylic acid 0.3 to 2.2% by weight, and More preferably, styrene is 97.8 to 99.7% by weight, particularly methacrylic acid and / or acrylic acid is 0.4 to 1.8% by weight, and styrene is 98.2 to 99.6% by weight. preferable.
- the method of copolymerizing the monomer mixture (b2) in the presence of the core polymer particles (A) on which the inner shell layer (B1) is formed is not particularly limited, but the inner shell layer (B1) is formed.
- a method in which the monomer mixture (b2) is emulsion-polymerized in an aqueous dispersion of the core polymer particles (A) is preferable, whereby the inner shell layer (B1) and the intermediate shell layer (B2) are formed.
- Core polymer particles (A) can be obtained.
- any of batch method, semi-continuous method and continuous method may be used, and the polymerization pressure, polymerization temperature and polymerization time are not particularly limited, and known conditions can be adopted.
- the auxiliary materials for polymerization exemplified in the production of the core polymer particles (A) and the formation of the inner shell layer (B1) can be used.
- Outer shell layer forming step In the outer shell layer forming step, the monomer mixture (b3) is added in the presence of the core polymer particles (A) on which the inner shell layer (B1) and the intermediate shell layer (B2) are formed. Copolymerize to form an outer shell layer (B3) that substantially surrounds the intermediate shell layer (B2).
- the content ratio of the acidic group-containing monomer in the monomer mixture (b3) is preferably 0.15% by weight or less, more preferably 0.1% by weight or less, and further preferably 0.05% by weight.
- the content ratio of the acidic group-containing monomer is preferably substantially zero. That is, it is preferable to use a monomer mixture (b3) that does not contain an acidic group-containing monomer.
- the acidic group-containing monomer is a monomer having a functional group exhibiting acidity, and representative examples include those exemplified for the core polymer particles (A) described above. .
- the content ratio of the acidic group-containing monomer is within the above range, the content ratio of the acidic group-containing monomer is too high, and the amount of aggregates in the aqueous dispersion of the hollow polymer particles is increased. The phenomenon can be suppressed.
- the monomer other than the acidic group-containing monomer contained in the monomer mixture (b3) is not particularly limited, but aromatics such as styrene, ⁇ -methylstyrene, p-methylstyrene, and halogenated styrene are used.
- Group vinyl monomers ethylenically unsaturated nitrile monomers such as acrylonitrile and methacrylonitrile; methyl (meth) acrylate, ethyl (meth) acrylate, butyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, lauryl ( Ethylenically unsaturated carboxylic acid ester monomers such as (meth) acrylate, glycidyl (meth) acrylate, 2-hydroxyethyl (meth) acrylate; (meth) acrylamide, N-methylol (meth) acrylamide, N-butoxymethyl (meta) ) Ethylenically unsaturated compounds such as acrylamide Boronamide monomers; Conjugated diene monomers such as butadiene and isoprene; Carboxylic acid vinyl ester monomers such as vinyl acetate; Vinyl halide monomers such as vinyl chloride; Vinylidene
- an aromatic vinyl monomer is preferable and styrene is more preferable because an aqueous dispersion of hollow polymer particles with a small amount of aggregates is easily obtained.
- a monomer mixture (b3) containing only an aromatic vinyl monomer it is preferable to use a monomer mixture containing only styrene.
- the method of copolymerizing the monomer mixture (b3) in the presence of the core polymer particles (A) in which the inner shell layer (B1) and the intermediate shell layer (B2) are formed is not particularly limited.
- a method in which the monomer mixture (b3) is emulsion-polymerized in an aqueous dispersion of the core polymer particles (A) on which the layer (B1) and the intermediate shell layer (B2) are formed is preferable.
- the core polymer particles (A) in which the layer (B1), the intermediate shell layer (B2), and the outer shell layer (B3) are formed can be obtained.
- any of batch method, semi-continuous method and continuous method may be used, and the polymerization pressure, polymerization temperature and polymerization time are not particularly limited, and known conditions can be adopted.
- the secondary materials for polymerization exemplified in the production of the core polymer particles (A) and the formation of the inner shell layer (B1) and the intermediate shell layer (B2) are used. I can.
- the weight ratio of the monomer mixture for forming the core polymer particles (A), the inner shell layer (B1), the intermediate shell layer (B2) and the outer shell layer (B3) is the effect of the present invention. Is more preferably obtained in a weight ratio of “monomer mixture (a) / monomer mixture (b1) / monomer mixture (b2) / monomer mixture (b3)”.
- the core swelling step and the shell swelling step are performed, but the shell swelling step may be performed after the core swelling step, or the shell swelling step. You may perform a core swelling process after performing.
- the porosity can be increased by a two-stage process including a core swelling process and a shell swelling process.
- the base is added to the aqueous dispersion containing the core polymer particles (A) on which the first shell layer (B) is formed, to the monomer mixture (a) and the monomer mixture.
- the core polymer particles (A) are swollen.
- the above amount of base is added to the aqueous dispersion containing the core polymer particles (A) on which the first shell layer (B) is formed, and the pH of the aqueous dispersion is 7 or more.
- the acidic groups contained in the core polymer particles (A) is neutralized to form voids.
- the base may be either a volatile base or a non-volatile base, and specific examples of the volatile base include ammonia, ammonium hydroxide, morpholine, trimethylamine, triethylamine and the like.
- Specific examples of the non-volatile base include alkali metal hydroxides such as sodium hydroxide, potassium hydroxide and lithium hydroxide; alkaline earth metal hydroxides such as calcium hydroxide and magnesium hydroxide; sodium carbonate, Examples include alkali metal (bi) carbonates such as potassium bicarbonate; (bi) ammonium carbonate salts such as ammonium carbonate and ammonium bicarbonate.
- volatile bases are preferable, and ammonia and ammonium hydroxide are more preferable.
- the base when adding the base, from the viewpoint of suppressing the generation of aggregates during the addition, it is preferably added in the form of an aqueous solution, and the concentration of the base in the aqueous solution is preferably 0.5 to 20 % By weight, more preferably 1 to 10% by weight.
- an anionic surfactant and / or a nonionic surfactant may be added before adding the base from the viewpoint of suppressing the generation of aggregates during the base treatment.
- the treatment time in performing the core swelling step may be a time required for the base to sufficiently diffuse inside the core polymer particles (A), and is usually 5 to 120 minutes, preferably 10 What is necessary is just to select suitably in the range for -90 minutes.
- the temperature during the core swelling step is preferably not less than the temperature at which the core polymer particles (A) are sufficiently softened from the viewpoint of diffusibility of the base, and preferably 70 to 95 ° C.
- the monomer mixture (c) is converted into an aqueous dispersion containing the core polymer particles (A) on which the first shell layer (B) is formed. And 0.1 to 45 parts by weight, preferably 1 to 40 parts by weight, more preferably 1 to 30 parts by weight, based on 100 parts by weight of the total amount of monomers contained in the monomer mixture (b), In this step, the first shell layer (B) is swollen. Since the first shell layer (B) is plasticized by performing the shell swelling step, the core polymer particles (A) can be swollen.
- the water content difference expressed by the water content of the core polymer particles (A) on which the first shell layer (B) is formed is 1 to 45%, preferably 3 to 40%.
- the water content is, for example, diluted by adding distilled water to an aqueous dispersion containing a predetermined solid content weight (Y (g)) of the core polymer particles (A) on which the first shell layer (B) is formed.
- the total weight is set to Z (g), and after centrifuging under a predetermined condition, all the supernatant water is taken out, and its weight (X (g)) is measured.
- a monomer mixture (c) The thing similar to the thing quoted by the said monomer mixture (b3) can be used.
- a monomer mixture (c) containing only an aromatic vinyl monomer it is preferable to use a monomer mixture containing only styrene.
- the treatment time when performing the shell swelling step is preferably 5 to 120 minutes.
- the temperature during the shell swelling step is preferably 10 to 95 ° C., particularly preferably 75 to 95 ° C., from the viewpoint of plasticizing the shell.
- the method for stopping the polymerization is not particularly limited, but it is preferable to stop the polymerization by adding a polymerization inhibitor.
- polymerization inhibitor examples include hydroxylamine, hydroxyamine sulfate, diethylhydroxyamine, hydroxyaminesulfonic acid and its alkali metal salt, sodium dimethyldithiocarbamate, and the like.
- the amount of the polymerization inhibitor used is not particularly limited, but is preferably 0.01 to 2 with respect to 100 parts by weight of the total monomers used for the polymerization of the core polymer particles (A) and the first shell layer (B). Parts by weight.
- the monomer mixture (c) is formed into the first shell layer (B), and the core polymer particles (A) and the first shell layer (B). It is preferable to carry out a second shell layer forming step in which a second shell layer (C) is formed by copolymerization in the presence of an aqueous dispersion containing the core polymer particles (A) swollen.
- the second shell layer (C) it is preferable to start polymerization of the monomer mixture (c) by adding a polymerization initiator after the core swelling step and the shell swelling step.
- azo compounds such as azobisisobutyronitrile; organic peroxides such as diisopropylbenzene hydroperoxide, cumene hydroperoxide, benzoyl peroxide, lauroyl peroxide; potassium persulfate, sodium persulfate, And inorganic peroxides such as ammonium persulfate.
- organic peroxides such as diisopropylbenzene hydroperoxide, cumene hydroperoxide, benzoyl peroxide, lauroyl peroxide
- potassium persulfate sodium persulfate
- inorganic peroxides such as ammonium persulfate.
- the formation of the core polymer particles (A), the formation of the first shell layer, the core swelling step, the shell swelling step and the formation of the second shell layer (C) are the same reactor. It may be carried out stepwise in the process, or after the previous step, the product obtained in the previous step may be transferred to another reactor and the next step may be performed. .
- steam saturated steam
- steam stripping may be performed.
- the steam stripping a conventionally known method can be used without limitation.
- the content ratio of the residual monomer contained in the aqueous dispersion of the hollow polymer particles is preferably 0.01% by weight or less.
- the pH and solid content concentration of the aqueous dispersion may be adjusted as necessary.
- the aqueous dispersion of hollow polymer particles obtained by the production method of the present invention has a number average particle diameter of the hollow polymer particles of preferably 0.5 to 2.0 ⁇ m, more preferably 0.8 to The thickness is 1.7 ⁇ m, more preferably 1.0 to 1.5 ⁇ m.
- the number average particle diameter of the hollow polymer particles can be determined, for example, by measuring the maximum particle diameter of each of the 200 hollow polymer particles with a transmission electron microscope and arithmetically averaging the measured particle diameter.
- the porosity of the hollow polymer particles is preferably 30 to 65%, more preferably 40 to 60%, and still more preferably 53 to 58%.
- the porosity of the hollow polymer particles is determined by measuring the maximum particle diameter and the maximum diameter of the voids for each of the 200 hollow polymer particles with a transmission electron microscope and arithmetically averaging the porosity obtained from the measurement results. Can do.
- the method for producing an aqueous dispersion of hollow polymer particles of the present invention it is possible to obtain hollow polymer particles having a high porosity and sufficient white paper gloss when used in the production of coated paper.
- Examples of the aqueous dispersion of hollow polymer particles obtained by the production method of the present invention include inorganic pigments such as calcium carbonate, clay, barium sulfate, calcium carbonate, talc, titanium oxide, satin white, aluminum hydroxide, silica, and mica. Can be used as a composition for coated paper. Furthermore, a coated paper can be obtained by applying such a composition for coated paper to a base paper to form a surface coating layer. The white paper gloss of the coated paper thus obtained preferably has a light reflectance of 80% or more.
- the coated paper having a layer containing hollow polymer particles obtained by the method for producing an aqueous dispersion of hollow polymer particles of the present invention has excellent white paper gloss and printing gloss, and has such characteristics. It can be suitably used for publications such as books and magazines and commercial printed materials such as flyers, brochures and posters.
- the paper on which the layer containing the hollow polymer particles obtained by the method for producing an aqueous dispersion of hollow polymer particles of the present invention forms a layer using heat due to the thermal properties of the air inside the hollow polymer particles. It can also be used for information recording papers such as heat-sensitive recording papers and thermal transfer papers that exhibit performance.
- the aqueous polymer dispersion was weighed so that the solid weight of the polymer particles obtained before and after the shell swelling step was 6.3 g, respectively. And placed in a centrifuge tube ( ⁇ 28.8, height 106.7 mm). Thereafter, it was diluted with distilled water to a total weight of 35 g. Centrifugation was performed with a centrifuge at a rotation speed of 18000 rpm and a rotation time of 60 minutes. Then, all the supernatant water was taken out and the weight (X (g)) was measured and calculated
- Solid content concentration of aqueous dispersion of hollow polymer particles 2 g of the aqueous dispersion of hollow polymer particles was taken out and placed in an aluminum dish. Then, it dried at 105 degreeC with the oven dryer for 2 hours. Then, the weight (Y (g)) of the residue which remained in the aluminum dish was measured and calculated
- Aggregate generation amount of aqueous dispersion of hollow polymer particles The aqueous dispersion containing hollow polymer particles corresponding to a total solid content of 150 g was filtered through a 200 mesh wire mesh, and the residue remaining on the wire mesh was washed with water. Then, it dried at 105 degreeC for 4 hours. Subsequently, the aggregate generation amount was evaluated by determining the ratio of the weight of the residue on the wire mesh to the total solid content of 150 g used for the filtration.
- Number average particle size of hollow polymer particles Using a transmission electron microscope, the maximum particle size of each of the 200 hollow polymer particles was measured, and the number average particle size was obtained by arithmetically averaging them.
- Porosity of hollow polymer particles The maximum particle diameter and the maximum void diameter of 200 hollow polymer particles were measured with a transmission electron microscope, and the value obtained by arithmetically averaging the “porosity” calculated by the following equation The “porosity” of the polymer particles was used.
- Example 1 Production of core polymer particles (A) In a pressure vessel equipped with a stirring device, 100 parts of a monomer (methyl methacrylate 50% by weight, butyl acrylate 10% by weight, methacrylic acid 40% by weight), polyoxy as a surfactant Sodium ethylene alkyl ether sulfate (alkyl group C 12 H 35 , ethylene oxide addition number 18) 0.9 parts, sodium tripolyphosphate 0. 15 parts and 80 parts of ion-exchanged water were added and stirred to prepare an emulsion of the monomer mixture (a) for forming the core polymer.
- a monomer methyl methacrylate 50% by weight, butyl acrylate 10% by weight, methacrylic acid 40% by weight
- polyoxy a surfactant
- Sodium ethylene alkyl ether sulfate alkyl group C 12 H 35 , ethylene oxide addition number 18
- sodium tripolyphosphate 0. 15 parts
- 80 parts of ion-exchanged water were added and
- the reaction was further continued for 2 hours to obtain an aqueous dispersion containing the core polymer particles (A) which is a swellable substance with respect to the base.
- the polymerization conversion rate at this time was 99%.
- the obtained core polymer particles (A) had a volume average particle diameter of 400 nm.
- each monomer mixture In a reaction vessel equipped with a stirrer, 100 parts of monomer (methyl methacrylate 78% by weight, butyl acrylate 16% by weight, methacrylic acid 6% by weight), polyoxyethylene alkyl ether sodium sulfate 0.2 part Then, 0.03 part of t-dodecyl mercaptan and 160 parts of ion-exchanged water were charged and then stirred to prepare an emulsion of the monomer mixture (b1) for forming the inner shell layer (B1).
- monomer methyl methacrylate 78% by weight, butyl acrylate 16% by weight, methacrylic acid 6% by weight
- polyoxyethylene alkyl ether sodium sulfate 0.2 part
- 0.03 part of t-dodecyl mercaptan and 160 parts of ion-exchanged water were charged and then stirred to prepare an emulsion of the monomer mixture (b1) for forming the inner shell layer (B1).
- first shell layer (B) (inner shell layer (B1), intermediate shell layer (B2) and outer shell layer (B3)), and in a reaction vessel with a stirrer, 250 parts of ion-exchanged water, and The aqueous dispersion containing the obtained core polymer particles (A) is prepared so that the weight of the core polymer particles (A) is about 10 parts (that is, the amount of the monomer mixture (a) used is 10 parts) and heated to 85 ° C. Next, 10 parts of a 4% by weight aqueous potassium persulfate solution was added to the reaction vessel, and then the emulsion of the monomer mixture (b1) for forming the first shell layer (B1) was maintained while maintaining the temperature at 85 ° C. The amount of the monomer mixture (b1) (10 parts) was continuously added to the reaction vessel over 20 minutes to polymerize to form the inner shell layer (B1).
- an emulsion of the monomer mixture (b2) for forming the intermediate shell layer (B2) (the amount of the monomer mixture (b2) is 49 parts) is added to the reaction vessel. Over 65 minutes, it was continuously added to the reaction vessel to polymerize to form an intermediate shell layer (B2).
- an emulsion of the monomer mixture (b3) for forming the outer shell layer (B3) (the amount of the monomer mixture (b3) is 41 parts) is added to the reaction vessel. Over 55 minutes, the outer shell layer (B3) was formed by polymerization by continuously adding to the reaction vessel.
- Core swelling process (base treatment) Immediately after forming the first shell layer (B) (inner shell layer (B1), intermediate shell layer (B2), and outer shell layer (B3)) in this order by the above-described method, 5 wt% ammonia was added to the reaction vessel.
- the core polymer particles (A) were swollen with a base by adding 20 parts of water and performing a base treatment at 90 ° C. for 1 hour.
- the pH of the reaction solution was 7 or more and 12 or less over 1 hour during the base treatment.
- the obtained polymer particles the core polymer particles (A) on which the first shell layer (B) is formed, the core polymer particles (A) The water content was measured. The results are shown in Table 1.
- Second shell layer forming step After passing through the shell swelling step by the method described above, 10 parts of a 4% by weight potassium persulfate aqueous solution is added, and the reaction is further continued for 4 hours to obtain an aqueous dispersion containing hollow polymer particles. Obtained. With respect to this aqueous dispersion, the solid content concentration and the aggregate generation amount were measured. The polymerization conversion rate at this time was 99%. The number average particle diameter and the porosity of the obtained hollow polymer particles were measured, and the results are shown in Table 1.
- Example 2 An aqueous dispersion of hollow polymer particles was obtained in the same manner as in Example 1 except that the amount of the monomer mixture (c) added in the shell swelling step was 15 parts (styrene: 15 parts). Further, the moisture content of the polymer particles before and after the shell swelling step, the moisture content difference, the solid content concentration of the aqueous dispersion of the hollow polymer particles, the amount of aggregates, the number average particle diameter and the porosity were measured. Indicated. Furthermore, a coated paper composition was prepared and a coated paper was prepared in the same manner as in Example 1, except that the type of hollow polymer particles used was changed to the hollow polymer particles obtained in Example 2. . About the obtained coated paper, the reflectance of light was measured. The results are shown in Table 1.
- Example 3 An aqueous dispersion of hollow polymer particles was obtained in the same manner as in Example 1 except that the amount of the monomer mixture (c) added in the shell swelling step was 30 parts (styrene: 30 parts). Further, the moisture content of the polymer particles before and after the shell swelling step, the moisture content difference, the solid content concentration of the aqueous dispersion of the hollow polymer particles, the amount of aggregates, the number average particle diameter and the porosity were measured. Indicated. Further, a coated paper composition was prepared and a coated paper was prepared in the same manner as in Example 1, except that the type of hollow polymer particles used was changed to the hollow polymer particles obtained in Example 3. . About the obtained coated paper, the reflectance of light was measured. The results are shown in Table 1.
- Example 4 An aqueous dispersion of hollow polymer particles was obtained in the same manner as in Example 1 except that 25 parts of 20 wt% aqueous ammonia was added in the core swelling step. Further, the moisture content of the polymer particles before and after the shell swelling step, the moisture content difference, the solid content concentration of the aqueous dispersion of the hollow polymer particles, the amount of aggregates, the number average particle diameter and the porosity were measured. Indicated. Further, a coated paper composition was prepared and a coated paper was prepared in the same manner as in Example 1, except that the type of hollow polymer particles used was changed to the hollow polymer particles obtained in Example 4. . About the obtained coated paper, the reflectance of light was measured. The results are shown in Table 1.
- Example 5 An aqueous dispersion of hollow polymer particles was obtained in the same manner as in Example 1 except that 50 parts of 20 wt% aqueous ammonia was added in the core swelling step. Further, the moisture content of the polymer particles before and after the shell swelling step, the moisture content difference, the solid content concentration of the aqueous dispersion of the hollow polymer particles, the amount of aggregates, the number average particle diameter and the porosity were measured. Indicated. Further, a coated paper composition was prepared and coated paper was prepared in the same manner as in Example 1, except that the type of hollow polymer particles used was changed to the hollow polymer particles obtained in Example 5. . About the obtained coated paper, the reflectance of light was measured. The results are shown in Table 1.
- Example 6 Production of the core polymer particles (A) and formation of the first shell layer (B) were performed in the same manner as in Example 1, and the order of the subsequent steps was changed. Specifically, after the production of the core polymer particles (A) and the formation of the first shell layer (B), the shell swelling step, the core swelling step and the second shell layer forming step were carried out in this order.
- the water content obtained before the shell swelling step was determined as the water content of the polymer particles.
- the water content of the coalesced particles (core polymer particles (A) on which the first shell layer (B) was formed) was measured. The results are shown in Table 2.
- a shell swelling step first, 0.65 parts of 10 wt% diethylhydroxyamine as a polymerization inhibitor was added to the reaction vessel. Ten minutes after the addition of the polymerization inhibitor, 10 parts (styrene: 10 parts) of the monomer mixture (c) was added to the reaction vessel.
- aqueous dispersion containing hollow polymer particles was obtained.
- the solid content concentration and aggregate generation amount of the aqueous dispersion of hollow polymer particles, the number average particle diameter and the void ratio of the hollow polymer particles were measured and shown in Table 2.
- a coated paper composition was prepared and a coated paper was prepared in the same manner as in Example 1, except that the type of hollow polymer particles used was changed to the hollow polymer particles obtained in Example 6. . About the obtained coated paper, the reflectance of light was measured. The results are shown in Table 2.
- Example 1 An aqueous dispersion of hollow polymer particles was obtained in the same manner as in Example 1 except that the shell swelling step was omitted. Further, the solid content concentration, aggregate generation amount, number average particle diameter and porosity of the aqueous dispersion of hollow polymer particles were measured and shown in Table 1. Although the shell swelling process is not performed, the water content of the polymer particles before the shell swelling process and the polymer particles after the shell swelling process is the core polymer particles (A) in which the first shell layer (B) is formed. The water content of the swollen core polymer particles (A) was measured. That is, the water content of the polymer particles before the shell swelling process and the polymer particles after the shell swelling process are both the same value. This value is shown in Table 1. Furthermore, although the moisture content difference of the polymer particles before and after the shell swelling step is shown in Table 1, since the moisture content does not change before and after the shell swelling step, the moisture content difference is indicated as “0”.
- Example 1 a coated paper composition was prepared and coated paper was prepared in the same manner as in Example 1 except that the type of hollow polymer particles used was changed to the hollow polymer particles obtained in Comparative Example 1. . About the obtained coated paper, the reflectance of light was measured. The results are shown in Table 1.
- Example 2 An aqueous dispersion of hollow polymer particles was obtained in the same manner as in Example 1 except that the polymerization inhibitor 10 wt% diethylhydroxyamine was not added in the shell swelling step. Further, the water content of the polymer particles before and after the shell swelling step, the solid content concentration of the aqueous dispersion of hollow polymer particles, the amount of aggregates, the number average particle diameter and the porosity were measured and shown in Table 1. Further, a coated paper composition was prepared and a coated paper was prepared in the same manner as in Example 1, except that the type of hollow polymer particles used was changed to the hollow polymer particles obtained in Comparative Example 2. . About the obtained coated paper, the reflectance of light was measured. The results are shown in Table 1.
- Example 3 An aqueous dispersion of hollow polymer particles was obtained in the same manner as in Example 1 except that 175 parts of 20 wt% aqueous ammonia was added in the core swelling step. Further, the water content of the polymer particles before and after the shell swelling step, the solid content concentration of the aqueous dispersion of hollow polymer particles, the amount of aggregates, the number average particle diameter and the porosity were measured and shown in Table 1. Further, a coated paper composition was prepared and a coated paper was prepared in the same manner as in Example 1, except that the type of hollow polymer particles used was changed to the hollow polymer particles obtained in Comparative Example 3. . About the obtained coated paper, the reflectance of light was measured. The results are shown in Table 1.
- Example 4 An aqueous dispersion of hollow polymer particles was obtained in the same manner as in Example 1 except that the core swelling step was omitted (that is, ammonia water was not added in the core swelling step). Further, the water content of the polymer particles before and after the shell swelling step, the solid content concentration of the aqueous dispersion of hollow polymer particles, the amount of aggregates, the number average particle diameter and the porosity were measured and shown in Table 1. Further, a coated paper composition was prepared and coated paper was prepared in the same manner as in Example 1 except that the type of hollow polymer particles used was changed to the hollow polymer particles obtained in Comparative Example 4. . About the obtained coated paper, the reflectance of light was measured. The results are shown in Table 1.
- Example 5 An attempt was made to produce an aqueous dispersion of hollow polymer particles in the same manner as in Example 1, except that the amount of the monomer mixture (c) added in the shell swelling step was 50 parts (styrene: 50 parts). Agglomerated after the shell swelling step. Therefore, the water content of the polymer particles after the shell swelling step, the solid content concentration of the aqueous dispersion of hollow polymer particles, the amount of aggregates, the number average particle diameter and the porosity could not be measured. Moreover, preparation of the composition for coated paper and preparation of coated paper could not be performed. In addition, it measured about the moisture content of the polymer particle before a shell swelling process. The results are shown in Table 1.
- the amount of ammonia added during the core swelling step is the monomer mixture (a) and the monomer mixture (b) (monomer mixture (b1), monomer mixture (b2) and
- the amount of the monomer mixture (c) used in the shell swelling step is in the range of 0.1 to 30 parts with respect to 100 parts of the total amount of monomers contained in the monomer mixture (b3)).
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Abstract
Description
(1) 単量体混合物(a)を共重合し、コア重合体粒子(A)を形成するコア形成工程と、単量体混合物(b)を、前記コア重合体粒子(A)の存在下で共重合し、前記コア重合体粒子(A)を実質的に包囲し、塩基に対して非膨潤である第1シェル層(B)を形成する第1シェル層形成工程と、塩基を、前記第1シェル層(B)が形成されたコア重合体粒子(A)を含有する水性分散液に、前記単量体混合物(a)及び前記単量体混合物(b)に含まれる単量体の合計量100重量部に対して0.1~30重量部添加し、前記コア重合体粒子(A)を膨潤させるコア膨潤工程と、単量体混合物(c)を、前記第1シェル層(B)が形成されたコア重合体粒子(A)を含有する水性分散液に、前記単量体混合物(a)及び前記単量体混合物(b)に含まれる単量体の合計量100重量部に対して0.1~45重量部添加し、前記第1シェル層(B)を膨潤させるシェル膨潤工程とを含み、(前記シェル膨潤工程後の前記第1シェル層(B)が形成されたコア重合体粒子(A)の含水率)-(前記シェル膨潤工程前の前記第1シェル層(B)が形成されたコア重合体粒子(A)の含水率)で表される含水率差が、1~45%である中空重合体粒子の水性分散液の製造方法、
(2) 前記コア膨潤工程及び前記シェル膨潤工程を行った後、前記単量体混合物(c)を、膨潤した前記コア重合体粒子(A)に、膨潤した前記第1シェル層(B)が形成されたコア重合体粒子(A)を含有する水性分散液の存在下で共重合し、第2シェル層(C)を形成する第2シェル層形成工程を含む(1)記載の中空重合体粒子の水性分散液の製造方法、
(3) 前記第1シェル層形成工程は、単量体混合物(b1)を、前記コア重合体粒子(A)の存在下で共重合し、前記コア重合体粒子(A)を実質的に包囲する内側シェル層(B1)を形成する内側シェル層形成工程と、単量体混合物(b2)を、前記内側シェル層(B1)が形成されたコア重合体粒子(A)の存在下で共重合し、前記内側シェル層(B1)を実質的に包囲する中間シェル層(B2)を形成する中間シェル層形成工程と、単量体混合物(b3)を、前記内側シェル層(B1)および前記中間シェル層(B2)が形成されたコア重合体粒子(A)の存在下で共重合し、前記中間シェル層(B2)を実質的に包囲する外側シェル層(B3)を形成する外側シェル層形成工程とを含む(1)または(2)記載の中空重合体粒子の水性分散液の製造方法、
(4) 前記単量体混合物(a)が、酸性基含有単量体20~50重量%、およびこれと共重合可能な単量体50~80重量%を含み、前記単量体混合物(b1)が、酸性基含有単量体1~10重量%、およびこれと共重合可能な単量体90~99重量%を含み、前記単量体混合物(b2)が、酸性基含有単量体0.2~2.5重量%、およびこれと共重合可能な単量体97.5~99.8重量%を含み、前記単量体混合物(b3)が、酸性基含有単量体0~0.15重量%、および酸性基含有単量体以外の単量体99.85~100重量%を含むことを特徴とする(3)に記載の中空重合体粒子の水性分散液の製造方法、
(5) 前記単量体混合物(a)、前記単量体混合物(b1)、前記単量体混合物(b2)および前記単量体混合物(b3)の割合を、「単量体混合物(a)/単量体混合物(b1)/単量体混合物(b2)/単量体混合物(b3)」の重量比で、(1~40)/(1~40)/(10~88)/(10~88)とすることを特徴とする(3)または(4)記載の中空重合体粒子の水性分散液の製造方法、
(6) (1)乃至(5)に記載の製造方法により得られた中空重合体粒子の水性分散液を用いてなる紙塗工用組成物、
(7) (6)記載の紙塗工用組成物を用いてなる塗工紙
が提供される。
本発明のコア形成工程においては、単量体混合物(a)を共重合し、コア重合体粒子(A)を形成する。
単量体混合物(a)中における、共重合可能な単量体の含有割合は、好ましくは50~80重量%であり、より好ましくは55~75重量%である。
本発明の第1シェル層形成工程においては、単量体混合物(b)を、前記コア重合体粒子(A)の存在下で共重合し、前記コア重合体粒子(A)を実質的に包囲し、塩基に対して非膨潤である第1シェル層(B)を形成する。ここで、塩基に対して非膨潤とは、塩基を添加する前後において、シェル層の含水率が変化しないことをいう。
シェル層が非膨潤である、即ちその含水率が塩基を添加する前後において変化しないことの確認は、シェル層を構成する単量体混合物を共重合させて密実の重合体粒子を作製して行う。具体的には、後述する含水率測定方法により、密実重合体粒子の含水率が塩基を添加する前後で変化しなければ、シェル層を形成した場合でも非膨潤となることが確認できる。ここで、第1シェル層(B)は、1層であってもよいし、2層以上から形成されていてもよい。第1シェル層(B)を形成する層の数は特に限定されないが、たとえば、第1シェル層(B)として、内側シェル層(B1)、中間シェル層(B2)および外側シェル層(B3)の3層から形成されるシェル層を採用することができる。
このような3層から形成される第1シェル層(B)は、単量体混合物(b1)を、前記コア重合体粒子(A)の存在下で共重合し、コア重合体粒子(A)を実質的に包囲する内側シェル層(B1)を形成する内側シェル層形成工程と、単量体混合物(b2)を、前記内側シェル層(B1)が形成されたコア重合体粒子(A)の存在下で共重合し、前記内側シェル層(B1)を実質的に包囲する中間シェル層(B2)を形成する中間シェル層形成工程と、単量体混合物(b3)を、前記内側シェル層(B1)および中間シェル層(B2)が形成されたコア重合体粒子(A)の存在下で共重合し、中間シェル層(B2)を実質的に包囲する外側シェル層(B3)を形成する外側シェル層形成工程により得ることができる。
以下、第1シェル層(B)が3層から形成される場合について説明する。
内側シェル層形成工程においては、単量体混合物(b1)を、前記コア重合体粒子(A)の存在下で共重合し、前記コア重合体粒子(A)を実質的に包囲する内側シェル層(B1)を形成する。
中間シェル層形成工程は、単量体混合物(b2)を、内側シェル層(B1)が形成されたコア重合体粒子(A)の存在下で共重合し、内側シェル層(B1)を実質的に包囲する中間シェル層(B2)を形成する。
外側シェル層形成工程においては、単量体混合物(b3)を、内側シェル層(B1)および中間シェル層(B2)が形成されたコア重合体粒子(A)の存在下で共重合し、中間シェル層(B2)を実質的に包囲する外側シェル層(B3)を形成する。
本発明においては、コア形成工程及び第1シェル層形成工程の後、コア膨潤工程およびシェル膨潤工程を行うが、コア膨潤工程を行ってからシェル膨潤工程を行ってもよいし、シェル膨潤工程を行ってからコア膨潤工程を行ってもよい。本発明においては、コア膨潤工程およびシェル膨潤工程の2段階の工程により空隙率を増大させることができる。
本発明のコア膨潤工程においては、塩基を、第1シェル層(B)が形成されたコア重合体粒子(A)を含有する水性分散液に、単量体混合物(a)及び単量体混合物(b)に含まれる単量体の合計量100重量部に対して0.1~30重量部、好ましくは0.5~20重量部、より好ましくは0.5~10重量部添加し、前記コア重合体粒子(A)を膨潤させる。
本発明におけるシェル膨潤工程は、単量体混合物(c)を、第1シェル層(B)が形成されたコア重合体粒子(A)を含有する水性分散液に、単量体混合物(a)及び単量体混合物(b)に含まれる単量体の合計量100重量部に対して0.1~45重量部、好ましくは1~40重量部、より好ましくは1~30重量部添加し、第1シェル層(B)を膨潤させる工程である。シェル膨潤工程を行うことにより、第1シェル層(B)が可塑化するため、コア重合体粒子(A)を膨潤させることができる。
下記の式
単量体混合物(c)としては、特に限定されないが、上記単量体混合物(b3)にて挙げたものと同様のものを用いることができる。
本発明においては、コア膨潤工程及びシェル膨潤工程の後、単量体混合物(c)を、第1シェル層(B)が形成され、コア重合体粒子(A)及び第1シェル層(B)が膨潤したコア重合体粒子(A)を含有する水性分散液の存在下で共重合し、第2シェル層(C)を形成する第2シェル層形成工程を行うことが好ましい。
また、試験および評価は、下記の方法で行った。
実施例および比較例において、シェル膨潤工程前およびシェル膨潤工程後にそれぞれ得られる重合体粒子の固形分重量が6.3gとなるように、前記水性重合体の分散液を量り取り、遠心管(Φ28.8、高さ106.7mm)に入れた。その後蒸留水にて全重量が35gになるように希釈した。遠心分離機にて、回転速度18000rpm、回転時間60分間遠心分離を行った。その後、上澄みの水を全て取り出し、その重量(X(g))を測定して求めた。これらの結果を踏まえ、下記の式により計算される値を重合体粒子の含水率とした。含水率が高い程、重合体粒子が水で膨潤していることを示す。
中空重合体粒子の水性分散液を2g取り出し、アルミ皿へ入れた。その後、オーブン乾燥器にて105℃にて2時間乾燥させた。その後、アルミ皿に残った残存物の重量(Y(g))を測定して求めた。これらの結果を踏まえ、下記の式により計算される値を中空重合体粒子の水性分散液の固形分濃度とした。
総固形分量150gに相当する中空重合体粒子を含有する水性分散液を、200メッシュの金網でろ過し、金網上に残存した残存物を水洗した後、105℃で4時間乾燥した。次いで、ろ過に用いた総固形分量150gに対する、金網上の残存物の重量の割合を百分率で求めることで、凝集物発生量を評価した。
透過型電子顕微鏡を用いて、中空重合体粒子200個につき各々の最大粒子径を測定し,それらを算術平均することで、数平均粒子径を求めた。
塗工紙について、グロスメーター(商品名「GM-26D」、村上色彩社製)を用いて、入射角75度、反射角75度の条件で塗工紙表面の光の反射率(単位:%)を測定した。得られた反射率の値が大きいほど、白紙光沢に優れていると判断できる。
コア重合体粒子(A)の製造
攪拌装置を備えた耐圧容器に、モノマー100部(メタクリル酸メチル50重量%、アクリル酸ブチル10重量%、メタクリル酸40重量%)、界面活性剤としてのポリオキシエチレンアルキルエーテル硫酸ナトリウム(アルキル基C12H35、エチレンオキサイド付加数18)0.9部、トリポリリン酸ナトリウム0 .15部、およびイオン交換水80部を添加し、攪拌して、コア重合体形成用の単量体混合物(a)の乳化物を調製した。
攪拌装置付き反応容器に、モノマー100部(メタクリル酸メチル78重量%、アクリル酸ブチル16重量%、メタクリル酸6重量%)、ポリオキシエチレンアルキルエーテル硫酸ナトリウム0.2部およびt-ドデシルメルカプタン0.03部、イオン交換水160部を仕込み、次いで攪拌することにより、内側シェル層(B1)形成用の単量体混合物(b1)の乳化物を調製した。
そして、攪拌装置付き反応容器に、イオン交換水250部、および上記にて得られたコア重合体粒子(A)を含む水性分散液を、コア重合体粒子(A)の重量が約10部となるように(すなわち、使用した単量体混合物(a)の配合量が、10部となるように)仕込み、85℃に昇温した。次いで、反応容器に、4重量%の過硫酸カリウム水溶液10部を添加し、その後、85℃に保ちながら、第1シェル層(B1)形成用の単量体混合物(b1)の乳化物(単量体混合物(b1)の量は10部)を、20分間に亘り、反応容器に連続的に添加することで、重合して内側シェル層(B1)を形成した。
上述した方法で、第1シェル層(B)(内側シェル層(B1)、中間シェル層(B2)および外側シェル層(B3))をこの順で形成した直後、反応容器に、5重量%アンモニア水20部を添加し、90℃で1時間の条件で塩基処理を行うことにより、塩基によりコア重合体粒子(A)を膨潤させた。なお、反応液のpHは、塩基処理中の1時間に亘って7以上12以下であった。また、シェル膨潤工程前重合体粒子の含水率として、得られた重合体粒子(第1シェル層(B)が形成されたコア重合体粒子(A)であって、コア重合体粒子(A)を膨潤させたもの)の含水率を測定した。結果を表1に示した。
上述した方法で、コア膨潤工程を経た後、反応容器に、重合禁止剤の10重量%ジエチルヒドロキシアミンを0.65部添加した。重合禁止剤を添加してから10分経過した後、反応容器に、単量体混合物(c)を5部(スチレン:5部)添加した。この状態で2時間経過させ、第1シェル層(B)を膨潤させた。また、シェル膨潤工程後重合体粒子の含水率として、得られた重合体粒子(第1シェル層(B)が形成されたコア重合体粒子(A)であって、コア重合体粒子(A)及び第1シェル層(B)を膨潤させたもの)の含水率を測定した。また、含水率差を下記式含水率差=(シェル膨潤工程後重合体粒子の含水率)-(シェル膨潤工程前重合体粒子の含水率)にて求めた。これらの結果を表1に示した。
上述した方法で、シェル膨潤工程を経た後、4重量%の過硫酸カリウム水溶液10部を添加し、さらに4時間反応を継続し、中空重合体粒子を含む水性分散液を得た。この水性分散液について固形分濃度及び凝集物発生量を測定した。なお、この際の重合転化率は99%であった。得られた中空重合体粒子の数平均粒子径、空隙率を測定し、結果を表1に示した。
攪拌装置を備えた耐圧容器に、無機顔料としてのカオリンクレイ(商品名「アストラコート」、イメリスミネラルズ・ジャパン社製)70部、無機顔料としての炭酸カルシウム(商品名「FMT90」、ファイマテック社製)30部、分散剤としてのポリアクリル酸ソーダ(商品名「アロンT-50」、東亞合成社製)0.15部、滑剤としてのステアリン酸カルシウム(商品名「ノプコートC-104HS」、サンノプコ社製)0.5部、燐酸エステル化澱粉(商品名「MS-4600」、日本食品化工社製)3部、および、カルボキシ変性スチレン-ブタジエン共重合体ラテックス(商品名「NipolLX407F」、日本ゼオン社製)9部を添加し、次いで、上記にて得られた中空重合体粒子を固形分で7部、およびイオン交換水を加えて混合・攪拌することで固形分濃度62%の塗工紙用組成物を得た。
得られた塗工紙用組成物を坪量65g/m2の原紙上に、片面に10g/m2にて塗布し、120℃で乾燥し、スーパーカレンダー処理して塗工紙を得た。得られた塗工紙の光の反射率の測定を行った。結果を表1に示す。
シェル膨潤工程にて加える単量体混合物(c)の量を15部(スチレン:15部)とした以外は、実施例1と同様にして、中空重合体粒子の水性分散液を得た。また、シェル膨潤工程前後の重合体粒子の含水率、含水率差、中空重合体粒子の水性分散液の固形分濃度、凝集物発生量、数平均粒子径および空隙率を測定し、表1に示した。さらに、用いる中空重合体粒子の種類を実施例2にて得られた中空重合体粒子に変更した以外は、実施例1と同様に塗工紙用組成物の調製および塗工紙作製を行った。得られた塗工紙について、光の反射率の測定を行った。結果を表1に示す。
シェル膨潤工程にて加える単量体混合物(c)の量を30部(スチレン:30部)とした以外は、実施例1と同様にして、中空重合体粒子の水性分散液を得た。また、シェル膨潤工程前後の重合体粒子の含水率、含水率差、中空重合体粒子の水性分散液の固形分濃度、凝集物発生量、数平均粒子径および空隙率を測定し、表1に示した。さらに、用いる中空重合体粒子の種類を実施例3にて得られた中空重合体粒子に変更した以外は、実施例1と同様に塗工紙用組成物の調製および塗工紙作製を行った。得られた塗工紙について、光の反射率の測定を行った。結果を表1に示す。
コア膨潤工程にて、20重量%アンモニア水25部を添加した以外は、実施例1と同様にして、中空重合体粒子の水性分散液を得た。また、シェル膨潤工程前後の重合体粒子の含水率、含水率差、中空重合体粒子の水性分散液の固形分濃度、凝集物発生量、数平均粒子径および空隙率を測定し、表1に示した。さらに、用いる中空重合体粒子の種類を実施例4にて得られた中空重合体粒子に変更した以外は、実施例1と同様に塗工紙用組成物の調製および塗工紙作製を行った。得られた塗工紙について、光の反射率の測定を行った。結果を表1に示す。
コア膨潤工程にて、20重量%アンモニア水50部を添加した以外は、実施例1と同様にして、中空重合体粒子の水性分散液を得た。また、シェル膨潤工程前後の重合体粒子の含水率、含水率差、中空重合体粒子の水性分散液の固形分濃度、凝集物発生量、数平均粒子径および空隙率を測定し、表1に示した。さらに、用いる中空重合体粒子の種類を実施例5にて得られた中空重合体粒子に変更した以外は、実施例1と同様に塗工紙用組成物の調製および塗工紙作製を行った。得られた塗工紙について、光の反射率の測定を行った。結果を表1に示す。
コア重合体粒子(A)の製造および第1シェル層(B)の形成については、実施例1と同様の方法で行い、その後の工程の順序を変更した。具体的には、コア重合体粒子(A)の製造および第1シェル層(B)の形成を行った後、シェル膨潤工程、コア膨潤工程および第2シェル層形成工程をこの順序で行った。
シェル膨潤工程を省略した以外は、実施例1と同様にして、中空重合体粒子の水性分散液を得た。また、中空重合体粒子の水性分散液の固形分濃度、凝集物発生量、数平均粒子径および空隙率を測定し、表1に示した。なお、シェル膨潤工程は行っていないが、シェル膨潤工程前重合体粒子およびシェル膨潤工程後重合体粒子の含水率として、第1シェル層(B)が形成されたコア重合体粒子(A)であって、コア重合体粒子(A)を膨潤させたものの含水率を測定した。即ち、シェル膨潤工程前重合体粒子とシェル膨潤工程後重合体粒子との含水率はどちらも同じ値となっている。この値を表1に示した。さらに、シェル膨潤工程前後の重合体粒子の含水率差を表1に示したが、上記よりシェル膨潤工程前後で含水率が変化しないため、含水率差を「0」として示した。
シェル膨潤工程にて、重合禁止剤の10重量%ジエチルヒドロキシアミンを添加しなかった以外は、実施例1と同様にして、中空重合体粒子の水性分散液を得た。また、シェル膨潤工程前後の重合体粒子の含水率、中空重合体粒子の水性分散液の固形分濃度、凝集物発生量、数平均粒子径および空隙率を測定し、表1に示した。さらに、用いる中空重合体粒子の種類を比較例2にて得られた中空重合体粒子に変更した以外は、実施例1と同様に塗工紙用組成物の調製および塗工紙作製を行った。得られた塗工紙について、光の反射率の測定を行った。結果を表1に示す。
コア膨潤工程にて、20重量%アンモニア水175部を添加した以外は、実施例1と同様にして、中空重合体粒子の水性分散液を得た。また、シェル膨潤工程前後の重合体粒子の含水率、中空重合体粒子の水性分散液の固形分濃度、凝集物発生量、数平均粒子径および空隙率を測定し、表1に示した。さらに、用いる中空重合体粒子の種類を比較例3にて得られた中空重合体粒子に変更した以外は、実施例1と同様に塗工紙用組成物の調製および塗工紙作製を行った。得られた塗工紙について、光の反射率の測定を行った。結果を表1に示す。
コア膨潤工程を省略したこと(即ち、コア膨潤工程においてアンモニア水を添加しなかったこと)以外は、実施例1と同様にして、中空重合体粒子の水性分散液を得た。また、シェル膨潤工程前後の重合体粒子の含水率、中空重合体粒子の水性分散液の固形分濃度、凝集物発生量、数平均粒子径および空隙率を測定し、表1に示した。さらに、用いる中空重合体粒子の種類を比較例4にて得られた中空重合体粒子に変更した以外は、実施例1と同様に塗工紙用組成物の調製および塗工紙作製を行った。得られた塗工紙について、光の反射率の測定を行った。結果を表1に示す。
シェル膨潤工程にて加える単量体混合物(c)の量を50部(スチレン:50部)とした以外は、実施例1と同様にして、中空重合体粒子の水性分散液の作製を試みたが、シェル膨潤工程後に凝集した。そのため、シェル膨潤工程後の重合体粒子の含水率、中空重合体粒子の水性分散液の固形分濃度、凝集物発生量、数平均粒子径および空隙率を測定することができなかった。また、塗工紙用組成物の調製および塗工紙作製についても行うことができなかった。なお、シェル膨潤工程前の重合体粒子の含水率については測定を行った。結果を表1に示す。
Claims (7)
- 単量体混合物(a)を共重合し、コア重合体粒子(A)を形成するコア形成工程と、
単量体混合物(b)を、前記コア重合体粒子(A)の存在下で共重合し、前記コア重合体粒子(A)を実質的に包囲し、塩基に対して非膨潤である第1シェル層(B)を形成する第1シェル層形成工程と、
塩基を、前記第1シェル層(B)が形成されたコア重合体粒子(A)を含有する水性分散液に、前記単量体混合物(a)及び前記単量体混合物(b)に含まれる単量体の合計量100重量部に対して0.1~30重量部添加し、前記コア重合体粒子(A)を膨潤させるコア膨潤工程と、
単量体混合物(c)を、前記第1シェル層(B)が形成されたコア重合体粒子(A)を含有する水性分散液に、前記単量体混合物(a)及び前記単量体混合物(b)に含まれる単量体の合計量100重量部に対して0.1~45重量部添加し、前記第1シェル層(B)を膨潤させるシェル膨潤工程と
を含み、
(前記シェル膨潤工程後の前記第1シェル層(B)が形成されたコア重合体粒子(A)の含水率)-(前記シェル膨潤工程前の前記第1シェル層(B)が形成されたコア重合体粒子(A)の含水率)
で表される含水率差が、1~45%である中空重合体粒子の水性分散液の製造方法。 - 前記コア膨潤工程及び前記シェル膨潤工程を行った後、前記単量体混合物(c)を、膨潤した前記コア重合体粒子(A)に、膨潤した前記第1シェル層(B)が形成されたコア重合体粒子(A)を含有する水性分散液の存在下で共重合し、第2シェル層(C)を形成する第2シェル層形成工程を含む請求項1記載の中空重合体粒子の水性分散液の製造方法。
- 前記第1シェル層形成工程は、単量体混合物(b1)を、前記コア重合体粒子(A)の存在下で共重合し、前記コア重合体粒子(A)を実質的に包囲する内側シェル層(B1)を形成する内側シェル層形成工程と、
単量体混合物(b2)を、前記内側シェル層(B1)が形成されたコア重合体粒子(A)の存在下で共重合し、前記内側シェル層(B1)を実質的に包囲する中間シェル層(B2)を形成する中間シェル層形成工程と、
単量体混合物(b3)を、前記内側シェル層(B1)および前記中間シェル層(B2)が形成されたコア重合体粒子(A)の存在下で共重合し、前記中間シェル層(B2)を実質的に包囲する外側シェル層(B3)を形成する外側シェル層形成工程と
を含む請求項1または2記載の中空重合体粒子の水性分散液の製造方法。 - 前記単量体混合物(a)が、酸性基含有単量体20~50重量%、およびこれと共重合可能な単量体50~80重量%を含み、
前記単量体混合物(b1)が、酸性基含有単量体1~10重量%、およびこれと共重合可能な単量体90~99重量%を含み、
前記単量体混合物(b2)が、酸性基含有単量体0.2~2.5重量%、およびこれと共重合可能な単量体97.5~99.8重量%を含み、
前記単量体混合物(b3)が、酸性基含有単量体0~0.15重量%、および酸性基含有単量体以外の単量体99.85~100重量%を含むことを特徴とする請求項3に記載の中空重合体粒子の水性分散液の製造方法。 - 前記単量体混合物(a)、前記単量体混合物(b1)、前記単量体混合物(b2)および前記単量体混合物(b3)の割合を、「単量体混合物(a)/単量体混合物(b1)/単量体混合物(b2)/単量体混合物(b3)」の重量比で、(1~40)/(1~40)/(10~88)/(10~88)とすることを特徴とする請求項3または4記載の中空重合体粒子の水性分散液の製造方法。
- 請求項1乃至5に記載の製造方法により得られた中空重合体粒子の水性分散液を用いてなる紙塗工用組成物。
- 請求項6記載の紙塗工用組成物を用いてなる塗工紙。
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JP2020158639A (ja) * | 2019-03-27 | 2020-10-01 | 日本ゼオン株式会社 | 中空重合体粒子の製造方法 |
JP2020158638A (ja) * | 2019-03-27 | 2020-10-01 | 日本ゼオン株式会社 | 中空重合体粒子の製造方法 |
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CN113152145B (zh) * | 2021-04-14 | 2022-04-01 | 浙江大学 | 一种含氮化硼导热填充剂的加热不燃烧卷烟纸的制备方法 |
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JPH07196747A (ja) * | 1991-12-13 | 1995-08-01 | Korea Chem Co Ltd | コア−殻乳化重合体の製造方法及びそれを含む分散組成物 |
JPH10182761A (ja) * | 1996-10-30 | 1998-07-07 | Nippon Zeon Co Ltd | 中空重合体粒子、その水性分散液およびそれらの製造方法 |
JP2002030113A (ja) * | 2000-05-09 | 2002-01-31 | Jsr Corp | 中空ポリマー粒子の製造方法 |
JP2002200846A (ja) * | 2000-12-28 | 2002-07-16 | Nippon Paper Industries Co Ltd | 感熱記録体 |
WO2015024882A1 (de) * | 2013-08-22 | 2015-02-26 | Basf Se | Verfahren zur herstellung von emulsionspolymerisaten |
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EP0959176B1 (en) * | 1998-05-18 | 2012-09-05 | Rohm And Haas Company | Hollow sphere organic pigment for paper or paper coatings |
KR100564807B1 (ko) * | 2004-07-06 | 2006-03-27 | 주식회사 엘지화학 | 중공 구조의 유화 중합체의 제조 방법 |
JP5333062B2 (ja) * | 2009-08-28 | 2013-11-06 | 日本ゼオン株式会社 | 中空重合体粒子を含有する水性分散液、その製造方法及び内添紙の製造方法 |
-
2016
- 2016-10-20 US US15/766,966 patent/US20180291561A1/en not_active Abandoned
- 2016-10-20 WO PCT/JP2016/081066 patent/WO2017073443A1/ja active Application Filing
- 2016-10-20 JP JP2017547757A patent/JP6760301B2/ja active Active
- 2016-10-20 EP EP16859673.2A patent/EP3369750A4/en not_active Withdrawn
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JPH07196747A (ja) * | 1991-12-13 | 1995-08-01 | Korea Chem Co Ltd | コア−殻乳化重合体の製造方法及びそれを含む分散組成物 |
JPH10182761A (ja) * | 1996-10-30 | 1998-07-07 | Nippon Zeon Co Ltd | 中空重合体粒子、その水性分散液およびそれらの製造方法 |
JP2002030113A (ja) * | 2000-05-09 | 2002-01-31 | Jsr Corp | 中空ポリマー粒子の製造方法 |
JP2002200846A (ja) * | 2000-12-28 | 2002-07-16 | Nippon Paper Industries Co Ltd | 感熱記録体 |
WO2015024882A1 (de) * | 2013-08-22 | 2015-02-26 | Basf Se | Verfahren zur herstellung von emulsionspolymerisaten |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2020158639A (ja) * | 2019-03-27 | 2020-10-01 | 日本ゼオン株式会社 | 中空重合体粒子の製造方法 |
JP2020158638A (ja) * | 2019-03-27 | 2020-10-01 | 日本ゼオン株式会社 | 中空重合体粒子の製造方法 |
Also Published As
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US20180291561A1 (en) | 2018-10-11 |
JPWO2017073443A1 (ja) | 2018-08-16 |
EP3369750A4 (en) | 2019-06-05 |
EP3369750A1 (en) | 2018-09-05 |
JP6760301B2 (ja) | 2020-09-23 |
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