JP4038487B2 - ポリマーの生産方法 - Google Patents
ポリマーの生産方法 Download PDFInfo
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- JP4038487B2 JP4038487B2 JP2004093348A JP2004093348A JP4038487B2 JP 4038487 B2 JP4038487 B2 JP 4038487B2 JP 2004093348 A JP2004093348 A JP 2004093348A JP 2004093348 A JP2004093348 A JP 2004093348A JP 4038487 B2 JP4038487 B2 JP 4038487B2
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- Prior art keywords
- polymer
- shell portion
- particles
- emulsion
- polymerization
- Prior art date
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- DDXLVDQZPFLQMZ-UHFFFAOYSA-M dodecyl(trimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)C DDXLVDQZPFLQMZ-UHFFFAOYSA-M 0.000 claims description 2
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- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 7
- CUTWSDAQYCQTGD-UHFFFAOYSA-N 2-prop-2-enoyloxypropanoic acid Chemical compound OC(=O)C(C)OC(=O)C=C CUTWSDAQYCQTGD-UHFFFAOYSA-N 0.000 description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 7
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- 239000003431 cross linking reagent Substances 0.000 description 6
- 229920001519 homopolymer Polymers 0.000 description 6
- IBDVWXAVKPRHCU-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)ethyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCCOC(=O)C(C)=C IBDVWXAVKPRHCU-UHFFFAOYSA-N 0.000 description 5
- MUWOTPLDXQSGQZ-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)propanoic acid Chemical compound OC(=O)C(C)OC(=O)C(C)=C MUWOTPLDXQSGQZ-UHFFFAOYSA-N 0.000 description 5
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- HCLJOFJIQIJXHS-UHFFFAOYSA-N 2-[2-[2-(2-prop-2-enoyloxyethoxy)ethoxy]ethoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCCOCCOC(=O)C=C HCLJOFJIQIJXHS-UHFFFAOYSA-N 0.000 description 4
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 4
- 239000004971 Cross linker Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 4
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- 125000002091 cationic group Chemical group 0.000 description 4
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- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 description 3
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 3
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- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
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- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 3
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- UOGPKCHLHAWNIY-UHFFFAOYSA-N [2-hydroxy-3-(2-hydroxy-3-prop-2-enoyloxypropoxy)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(O)COCC(O)COC(=O)C=C UOGPKCHLHAWNIY-UHFFFAOYSA-N 0.000 description 3
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- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 3
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- 125000004432 carbon atom Chemical group C* 0.000 description 3
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- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 3
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- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Chemical compound CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 231100000206 health hazard Toxicity 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 229920000140 heteropolymer Polymers 0.000 description 1
- LPTIRUACFKQDHZ-UHFFFAOYSA-N hexadecyl sulfate;hydron Chemical compound CCCCCCCCCCCCCCCCOS(O)(=O)=O LPTIRUACFKQDHZ-UHFFFAOYSA-N 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 150000001261 hydroxy acids Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical class C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- UEGPKNKPLBYCNK-UHFFFAOYSA-L magnesium acetate Chemical compound [Mg+2].CC([O-])=O.CC([O-])=O UEGPKNKPLBYCNK-UHFFFAOYSA-L 0.000 description 1
- 239000011654 magnesium acetate Substances 0.000 description 1
- 235000011285 magnesium acetate Nutrition 0.000 description 1
- 229940069446 magnesium acetate Drugs 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 235000011147 magnesium chloride Nutrition 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- NKHAVTQWNUWKEO-IHWYPQMZSA-N methyl hydrogen fumarate Chemical compound COC(=O)\C=C/C(O)=O NKHAVTQWNUWKEO-IHWYPQMZSA-N 0.000 description 1
- LUCXVPAZUDVVBT-UHFFFAOYSA-N methyl-[3-(2-methylphenoxy)-3-phenylpropyl]azanium;chloride Chemical compound Cl.C=1C=CC=CC=1C(CCNC)OC1=CC=CC=C1C LUCXVPAZUDVVBT-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- NKHAVTQWNUWKEO-NSCUHMNNSA-N monomethyl fumarate Chemical compound COC(=O)\C=C\C(O)=O NKHAVTQWNUWKEO-NSCUHMNNSA-N 0.000 description 1
- 229940005650 monomethyl fumarate Drugs 0.000 description 1
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 description 1
- XGHNWFFWGDCAHZ-UHFFFAOYSA-N n-(3-trimethoxysilylpropyl)prop-2-enamide Chemical compound CO[Si](OC)(OC)CCCNC(=O)C=C XGHNWFFWGDCAHZ-UHFFFAOYSA-N 0.000 description 1
- UTSYWKJYFPPRAP-UHFFFAOYSA-N n-(butoxymethyl)prop-2-enamide Chemical compound CCCCOCNC(=O)C=C UTSYWKJYFPPRAP-UHFFFAOYSA-N 0.000 description 1
- 239000001272 nitrous oxide Substances 0.000 description 1
- 229920002113 octoxynol Polymers 0.000 description 1
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920005787 opaque polymer Polymers 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- UCUUFSAXZMGPGH-UHFFFAOYSA-N penta-1,4-dien-3-one Chemical compound C=CC(=O)C=C UCUUFSAXZMGPGH-UHFFFAOYSA-N 0.000 description 1
- DBSDMAPJGHBWAL-UHFFFAOYSA-N penta-1,4-dien-3-ylbenzene Chemical compound C=CC(C=C)C1=CC=CC=C1 DBSDMAPJGHBWAL-UHFFFAOYSA-N 0.000 description 1
- YOTGRUGZMVCBLS-UHFFFAOYSA-N pentadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCOC(=O)C(C)=C YOTGRUGZMVCBLS-UHFFFAOYSA-N 0.000 description 1
- 235000020030 perry Nutrition 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- FSDNTQSJGHSJBG-UHFFFAOYSA-N piperidine-4-carbonitrile Chemical compound N#CC1CCNCC1 FSDNTQSJGHSJBG-UHFFFAOYSA-N 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004597 plastic additive Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 150000003077 polyols Chemical group 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 239000011164 primary particle Substances 0.000 description 1
- YOKDQEBPBYOXHX-UHFFFAOYSA-N prop-1-en-2-ylphosphonic acid Chemical compound CC(=C)P(O)(O)=O YOKDQEBPBYOXHX-UHFFFAOYSA-N 0.000 description 1
- UIIIBRHUICCMAI-UHFFFAOYSA-N prop-2-ene-1-sulfonic acid Chemical compound OS(=O)(=O)CC=C UIIIBRHUICCMAI-UHFFFAOYSA-N 0.000 description 1
- AZIQALWHRUQPHV-UHFFFAOYSA-N prop-2-eneperoxoic acid Chemical compound OOC(=O)C=C AZIQALWHRUQPHV-UHFFFAOYSA-N 0.000 description 1
- SOCRHXPOMLIEFC-UHFFFAOYSA-N prop-2-enoic acid hydrofluoride Chemical compound F.OC(=O)C=C.OC(=O)C=C SOCRHXPOMLIEFC-UHFFFAOYSA-N 0.000 description 1
- POSICDHOUBKJKP-UHFFFAOYSA-N prop-2-enoxybenzene Chemical compound C=CCOC1=CC=CC=C1 POSICDHOUBKJKP-UHFFFAOYSA-N 0.000 description 1
- YOSXAXYCARLZTR-UHFFFAOYSA-N prop-2-enoyl isocyanate Chemical compound C=CC(=O)N=C=O YOSXAXYCARLZTR-UHFFFAOYSA-N 0.000 description 1
- RZKYDQNMAUSEDZ-UHFFFAOYSA-N prop-2-enylphosphonic acid Chemical compound OP(O)(=O)CC=C RZKYDQNMAUSEDZ-UHFFFAOYSA-N 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- RSVDRWTUCMTKBV-UHFFFAOYSA-N sbb057044 Chemical compound C12CC=CC2C2CC(OCCOC(=O)C=C)C1C2 RSVDRWTUCMTKBV-UHFFFAOYSA-N 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 235000011083 sodium citrates Nutrition 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- HFQQZARZPUDIFP-UHFFFAOYSA-M sodium;2-dodecylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O HFQQZARZPUDIFP-UHFFFAOYSA-M 0.000 description 1
- MNCGMVDMOKPCSQ-UHFFFAOYSA-M sodium;2-phenylethenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C=CC1=CC=CC=C1 MNCGMVDMOKPCSQ-UHFFFAOYSA-M 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 230000000475 sunscreen effect Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- CNALVHVMBXLLIY-IUCAKERBSA-N tert-butyl n-[(3s,5s)-5-methylpiperidin-3-yl]carbamate Chemical compound C[C@@H]1CNC[C@@H](NC(=O)OC(C)(C)C)C1 CNALVHVMBXLLIY-IUCAKERBSA-N 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- ATZHWSYYKQKSSY-UHFFFAOYSA-N tetradecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCOC(=O)C(C)=C ATZHWSYYKQKSSY-UHFFFAOYSA-N 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 235000013337 tricalcium citrate Nutrition 0.000 description 1
- XHGIFBQQEGRTPB-UHFFFAOYSA-N tris(prop-2-enyl) phosphate Chemical compound C=CCOP(=O)(OCC=C)OCC=C XHGIFBQQEGRTPB-UHFFFAOYSA-N 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- ZTWTYVWXUKTLCP-UHFFFAOYSA-N vinylphosphonic acid Chemical compound OP(O)(=O)C=C ZTWTYVWXUKTLCP-UHFFFAOYSA-N 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
- 238000011179 visual inspection Methods 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/12—Powdering or granulating
- C08J3/16—Powdering or granulating by coagulating dispersions
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B9/00—Making granules
- B29B9/08—Making granules by agglomerating smaller particles
-
- 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
- C08F6/00—Post-polymerisation treatments
- C08F6/14—Treatment of polymer emulsions
- C08F6/22—Coagulation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/12—Powdering or granulating
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Mechanical Engineering (AREA)
- Engineering & Computer Science (AREA)
- Dispersion Chemistry (AREA)
- Graft Or Block Polymers (AREA)
- Cosmetics (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Description
1/Tg(計算値)=w(M1)/Tg(M1)+w(M2)/Tg(M2)
(式中、Tg(計算値)は、コポリマーについて計算したガラス転移温度であり、
w(M1)は、コポリマー中のモノマーM1の重量分率であり、
w(M2)は、コポリマー中のモノマーM2の重量分率であり、
Tg(M1)は、M1のホモポリマーのガラス転移温度であり、
Tg(M2)は、M2のホモポリマーのガラス転移温度であり、
全ての温度は、°Kである)
である。
(a)1種又は2種以上のエマルジョンポリマーを含有する第一水性ポリマー分散液を製造するステップと、
(b)第一水性ポリマー分散液を、1種又は2種以上のカチオン性界面活性剤(ここで、1種又は2種以上の凝結剤と組み合わせた、1種又は2種以上のカチオン性界面活性剤も包含する)によって凝結させて、凝結したスラリーを形成するステップと、
(c)1種又は2種以上のエマルジョンポリマーを含有する第二水性ポリマー分散液を、この凝結したスラリーに添加するステップと、及び
(d)この凝結したスラリーを乾燥して、自由流動性ポリマー固体を形成するステップと
を含む流動性非ダスティングポリマー固体の製造方法であって、得られるポリマー固体が、増加した粒子サイズ、増加したMIE、低下した又は変化しないMEP及び低下したKst値を有する方法を提供する。
およびASTM規格E1226(1991年)(非特許文献5)で特定された試験条件に従って測定した。全ての測定は、チルウォース・テクノロジー社(Chilworth Technology,Inc.)、ニュージャージー州モンマス・ジャンクション(Monmouth Junction)によって実施された。この試験は、それぞれの場合に最大圧力値が得られる、濃度の広い範囲に亘って行われる。最小発火エネルギー(MIE)は、ポリマーダスト雲の発火をもたらすことができる容量放電の手段によって得られる最低電気誘導発火エネルギーである。使用した試験装置は、1リットル体積のハルトマン垂直チューブ(Hartmann Vertical Tube)であり、測定は、ASTM E2019規格試験方法(非特許文献6)、英国規格方法BS5958、パート1(1991年)(非特許文献7)、進歩報告書VDI、シリーズ3:プロセス工学第134号(Fortschritt−Bereichte VDI, Reihe 3: Verfahrentechnik Nr 134)、独国(非特許文献8)に従って実施した。エネルギーは、式E=1/2CV2(式中、Cは、放電回路に接続されたキャパシタの電気キャパシタンスであり、そしてVは適用された電圧である)から計算される。
MMA=メタクリル酸メチル
BMA=メタクリル酸ブチル
ALMA=メタクリル酸アリル
MAA=メタクリル酸
DVB=ジビニルベンゼン(80%活性、20%エチルビニルベンゼン)
Sty=スチレン
SSS=スチレンスルホン酸ナトリウム
AAEM=メタクリル酸アセトアセトキシエチル
SDBS=ドデシルベンゼンスルホン酸ナトリウム
TMPTA=トリメチロールプロパン トリアクリレート
TEGDA=テトラエチレングリコール ジアクリレート
PBW=重量部
XL=架橋剤
NA=分析せず
MFM=多官能性モノマー
Claims (7)
- (a)硬質シェルを有し粒子サイズが0.05〜1マイクロメートルの多段エマルジョン粒子である、1種又は2種以上のエマルジョンポリマーを、1種又は2種以上のカチオン性界面活性剤によって凝結させる工程及び(b)この凝結物を乾燥する工程を含む、減少したダスティングを有する乾燥ポリマー組成物の生産方法であって;
前記エマルジョンポリマーが、(i)シェル部分の全重量基準で、4〜80パーセントのモノマー単位の1種又は2種以上の多エチレン性不飽和モノマーを含有させるための重合並びに(ii)シェル部分の全重量基準で、4〜80パーセントのモノマー単位の、ビニル共重合が可能な少なくとも1種の官能基及び重合後架橋を作るために有効な反応性分子との反応が可能な少なくとも1種の官能基を有する、1種又は2種以上の多官能性モノマーを含有させるための重合から選択された、1個又は2個以上のステップによって製造されたシェル部分を含むラテックスポリマー粒子から製造される、乾燥ポリマー組成物の生産方法。 - 乾燥ポリマー組成物が、界面活性剤を含有しないそれぞれのポリマー組成物と比較したとき、増加した最小発火エネルギー及びより低い爆発強度値を示す、請求項1記載の方法。
- カチオン性界面活性剤を、金属塩、有機化合物の金属塩、有機酸の金属塩、無機酸の金属塩、非イオン性界面活性剤、双性イオン性界面活性剤及びこれらの組合せ物からなる群から選択された1種又は2種以上の他の凝結剤と組み合わせて使用する、請求項1記載の方法。
- カチオン性界面活性剤が、(C12〜C20)アミン化合物、ラウリルピリジニウムクロリド、オクチルベンジルトリメチルアンモニウムクロリド、ヘキサデシルトリメチルアンモニウムクロリド、ヘキサデシルトリメチルアンモニウムブロミド、ドデシルトリメチルアンモニウムクロリド、酸素含有アミン、第四級アミン塩及び第四級アミン塩のエステルから選択される、請求項1記載の方法。
- 前記シェル部分が、(i)シェル部分の全重量基準で、10〜60パーセントのモノマー単位の1種又は2種以上の多エチレン性不飽和モノマーを含有させるための重合並びに(ii)シェル部分の全重量基準で、10〜60パーセントのモノマー単位の、ビニル共重合が可能な少なくとも1種の官能基及び重合後架橋を作るために有効な反応性分子との反応が可能な少なくとも1種の官能基を有する、1種又は2種以上の多官能性モノマーを含有させるための重合から選択された、1個又は2個以上のステップによって製造される、請求項1記載の方法。
- 前記ラテックスポリマー粒子の最外シェル部分が、最外シェル部分の重量基準で、15〜70%の架橋レベルを有する、請求項5記載の方法。
- 前記最外シェル部分が、前記シェル部分の少なくとも25%を構成する、請求項6記載の方法。
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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EP03292061 | 2003-08-21 |
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JP2005068400A JP2005068400A (ja) | 2005-03-17 |
JP4038487B2 true JP4038487B2 (ja) | 2008-01-23 |
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JP2004093348A Expired - Fee Related JP4038487B2 (ja) | 2003-08-21 | 2004-03-26 | ポリマーの生産方法 |
Country Status (6)
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---|---|
US (1) | US20050043453A1 (ja) |
JP (1) | JP4038487B2 (ja) |
KR (1) | KR100632501B1 (ja) |
CN (1) | CN1590436A (ja) |
AU (1) | AU2004203665A1 (ja) |
CA (1) | CA2477356A1 (ja) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
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US9765211B2 (en) | 2013-04-23 | 2017-09-19 | Rohm And Haas Company | Polymeric powder composition and a method of producing same |
KR101644675B1 (ko) * | 2013-05-03 | 2016-08-02 | 주식회사 엘지화학 | 유화중합 라텍스 응집제, 응집 방법 및 압사출 성형품의 제조방법 |
KR102489409B1 (ko) * | 2019-08-16 | 2023-01-17 | 주식회사 엘지화학 | 비닐시안 화합물-공액디엔 화합물-방향족 비닐 화합물 그라프트 공중합체의 제조방법 및 이 그라프트 공중합체를 포함하는 열가소성 수지 조성물 |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3971835A (en) * | 1970-07-17 | 1976-07-27 | Rohm And Haas Company | Vinyl halide polymer impact modifiers |
US3793402A (en) * | 1971-11-05 | 1974-02-19 | F Owens | Low haze impact resistant compositions containing a multi-stage,sequentially produced polymer |
US4427836A (en) * | 1980-06-12 | 1984-01-24 | Rohm And Haas Company | Sequential heteropolymer dispersion and a particulate material obtainable therefrom, useful in coating compositions as a thickening and/or opacifying agent |
US4569991A (en) * | 1982-01-26 | 1986-02-11 | Mitsubishi Monsanto Chemical Company | Production of thermoplastic resin |
US4468825A (en) * | 1983-01-28 | 1984-09-04 | Hobbs James R | Oxygen removal system for a bed |
US4594363A (en) * | 1985-01-11 | 1986-06-10 | Rohm And Haas Company | Production of core-sheath polymer particles containing voids, resulting product and use |
US4677003A (en) * | 1985-04-30 | 1987-06-30 | Rohm And Haas Company | Microsuspension process for preparing solvent core sequential polymer dispersion |
JPH0721011B2 (ja) * | 1987-06-25 | 1995-03-08 | 日本ゼオン株式会社 | 中空重合体粒子の製造方法 |
GB8718036D0 (en) * | 1987-07-30 | 1987-09-03 | Tioxide Group Plc | Polymeric particles |
US4970241A (en) * | 1988-05-20 | 1990-11-13 | Rohm And Haas Company | Multi-stage opacifying polymer particles containing non-polymeric acid absorbed therein |
US4970037A (en) * | 1989-10-31 | 1990-11-13 | E. I. Du Pont De Nemours And Company | Process for the manufacture of photosensitive materials having a low heat history |
US5157084A (en) * | 1990-10-12 | 1992-10-20 | The Dow Chemical Company | Process of making hollow polymer latex particles |
US5534594A (en) * | 1994-12-05 | 1996-07-09 | Rohm And Haas Company | Preparation of butadiene-based impact modifiers |
CA2322345A1 (en) * | 1999-10-14 | 2001-04-14 | Rohm And Haas Company | Method for preparing ultraviolet radiation-absorbing compositions |
JP3935315B2 (ja) * | 1999-11-01 | 2007-06-20 | キヤノン株式会社 | 重合法トナーの製造方法 |
-
2004
- 2004-03-26 JP JP2004093348A patent/JP4038487B2/ja not_active Expired - Fee Related
- 2004-07-22 US US10/896,468 patent/US20050043453A1/en not_active Abandoned
- 2004-08-09 AU AU2004203665A patent/AU2004203665A1/en not_active Abandoned
- 2004-08-11 CA CA002477356A patent/CA2477356A1/en not_active Abandoned
- 2004-08-11 CN CNA2004100565817A patent/CN1590436A/zh active Pending
- 2004-08-20 KR KR1020040066054A patent/KR100632501B1/ko not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
CA2477356A1 (en) | 2005-02-21 |
JP2005068400A (ja) | 2005-03-17 |
KR100632501B1 (ko) | 2006-10-09 |
US20050043453A1 (en) | 2005-02-24 |
CN1590436A (zh) | 2005-03-09 |
KR20050021250A (ko) | 2005-03-07 |
AU2004203665A1 (en) | 2005-03-10 |
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