JPS6037129B2 - 樹脂状重合体から未反応単量体の除去および回収法 - Google Patents
樹脂状重合体から未反応単量体の除去および回収法Info
- Publication number
- JPS6037129B2 JPS6037129B2 JP50041120A JP4112075A JPS6037129B2 JP S6037129 B2 JPS6037129 B2 JP S6037129B2 JP 50041120 A JP50041120 A JP 50041120A JP 4112075 A JP4112075 A JP 4112075A JP S6037129 B2 JPS6037129 B2 JP S6037129B2
- Authority
- JP
- Japan
- Prior art keywords
- monomer
- water
- polymer
- temperature
- weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000000178 monomer Substances 0.000 title claims description 59
- 229920000642 polymer Polymers 0.000 title claims description 56
- 238000000034 method Methods 0.000 title claims description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 45
- 229920000126 latex Polymers 0.000 claims description 28
- 239000004816 latex Substances 0.000 claims description 27
- 239000002245 particle Substances 0.000 claims description 17
- 150000002825 nitriles Chemical class 0.000 claims description 15
- 238000005406 washing Methods 0.000 claims description 13
- 239000002002 slurry Substances 0.000 claims description 11
- 229920001577 copolymer Polymers 0.000 claims description 7
- 230000008569 process Effects 0.000 claims description 7
- 239000007864 aqueous solution Substances 0.000 claims description 5
- 150000001993 dienes Chemical class 0.000 claims description 5
- 238000007720 emulsion polymerization reaction Methods 0.000 claims description 4
- 238000001035 drying Methods 0.000 claims description 3
- 229920001519 homopolymer Polymers 0.000 claims description 3
- 230000001112 coagulating effect Effects 0.000 claims description 2
- 229920003244 diene elastomer Polymers 0.000 claims description 2
- 239000003792 electrolyte Substances 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- 238000005345 coagulation Methods 0.000 description 38
- 230000015271 coagulation Effects 0.000 description 38
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 19
- 239000011347 resin Substances 0.000 description 19
- 229920005989 resin Polymers 0.000 description 19
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 13
- 239000007787 solid Substances 0.000 description 11
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 10
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 10
- UZKWTJUDCOPSNM-UHFFFAOYSA-N 1-ethenoxybutane Chemical compound CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 8
- 125000000217 alkyl group Chemical group 0.000 description 8
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- 229920001971 elastomer Polymers 0.000 description 8
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 7
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 6
- 238000004140 cleaning Methods 0.000 description 6
- 239000000701 coagulant Substances 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 4
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 4
- 229910052736 halogen Inorganic materials 0.000 description 4
- 150000002367 halogens Chemical class 0.000 description 4
- 150000002431 hydrogen Chemical group 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 4
- OVGRCEFMXPHEBL-UHFFFAOYSA-N 1-ethenoxypropane Chemical compound CCCOC=C OVGRCEFMXPHEBL-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 3
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 3
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 239000012736 aqueous medium Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- -1 etc. nal Chemical compound 0.000 description 3
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 108090000623 proteins and genes Proteins 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical compound CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 2
- WWUVJRULCWHUSA-UHFFFAOYSA-N 2-methyl-1-pentene Chemical compound CCCC(C)=C WWUVJRULCWHUSA-UHFFFAOYSA-N 0.000 description 2
- IRUDSQHLKGNCGF-UHFFFAOYSA-N 2-methylhex-1-ene Chemical compound CCCCC(C)=C IRUDSQHLKGNCGF-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 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 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 239000013505 freshwater Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- WAEOXIOXMKNFLQ-UHFFFAOYSA-N 1-methyl-4-prop-2-enylbenzene Chemical group CC1=CC=C(CC=C)C=C1 WAEOXIOXMKNFLQ-UHFFFAOYSA-N 0.000 description 1
- MHNNAWXXUZQSNM-UHFFFAOYSA-N 2-methylbut-1-ene Chemical compound CCC(C)=C MHNNAWXXUZQSNM-UHFFFAOYSA-N 0.000 description 1
- TVONJMOVBKMLOM-UHFFFAOYSA-N 2-methylidenebutanenitrile Chemical compound CCC(=C)C#N TVONJMOVBKMLOM-UHFFFAOYSA-N 0.000 description 1
- FBEDQPGLIKZGIN-UHFFFAOYSA-N 2-methyloct-1-ene Chemical compound CCCCCCC(C)=C FBEDQPGLIKZGIN-UHFFFAOYSA-N 0.000 description 1
- OAOZZYBUAWEDRA-UHFFFAOYSA-N 3,4-dimethylidenehexane Chemical compound CCC(=C)C(=C)CC OAOZZYBUAWEDRA-UHFFFAOYSA-N 0.000 description 1
- IGLWCQMNTGCUBB-UHFFFAOYSA-N 3-methylidenepent-1-ene Chemical compound CCC(=C)C=C IGLWCQMNTGCUBB-UHFFFAOYSA-N 0.000 description 1
- RYKZRKKEYSRDNF-UHFFFAOYSA-N 3-methylidenepentane Chemical compound CCC(=C)CC RYKZRKKEYSRDNF-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 229940037003 alum Drugs 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 210000000481 breast Anatomy 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 229920000547 conjugated polymer Polymers 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- MPOGZNTVZCEKSW-UHFFFAOYSA-N ethenyl 2-hydroxypropanoate Chemical compound CC(O)C(=O)OC=C MPOGZNTVZCEKSW-UHFFFAOYSA-N 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- CVUNPKSKGHPMSY-UHFFFAOYSA-N ethyl 2-chloroprop-2-enoate Chemical compound CCOC(=O)C(Cl)=C CVUNPKSKGHPMSY-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 210000000416 exudates and transudate Anatomy 0.000 description 1
- 210000003128 head Anatomy 0.000 description 1
- LNCPIMCVTKXXOY-UHFFFAOYSA-N hexyl 2-methylprop-2-enoate Chemical compound CCCCCCOC(=O)C(C)=C LNCPIMCVTKXXOY-UHFFFAOYSA-N 0.000 description 1
- LNMQRPPRQDGUDR-UHFFFAOYSA-N hexyl prop-2-enoate Chemical compound CCCCCCOC(=O)C=C LNMQRPPRQDGUDR-UHFFFAOYSA-N 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- GYDSPAVLTMAXHT-UHFFFAOYSA-N pentyl 2-methylprop-2-enoate Chemical compound CCCCCOC(=O)C(C)=C GYDSPAVLTMAXHT-UHFFFAOYSA-N 0.000 description 1
- ULDDEWDFUNBUCM-UHFFFAOYSA-N pentyl prop-2-enoate Chemical compound CCCCCOC(=O)C=C ULDDEWDFUNBUCM-UHFFFAOYSA-N 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-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
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 210000001747 pupil Anatomy 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000005201 scrubbing Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- 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
- C08F6/16—Purification
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Graft Or Block Polymers (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US460339 | 1974-04-12 | ||
| US05/460,339 US3954910A (en) | 1974-04-12 | 1974-04-12 | Process for removal and recovery of unreacted monomers from resinous polymers |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS50136379A JPS50136379A (en, 2012) | 1975-10-29 |
| JPS6037129B2 true JPS6037129B2 (ja) | 1985-08-24 |
Family
ID=23828311
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP50041120A Expired JPS6037129B2 (ja) | 1974-04-12 | 1975-04-04 | 樹脂状重合体から未反応単量体の除去および回収法 |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US3954910A (en, 2012) |
| JP (1) | JPS6037129B2 (en, 2012) |
| AR (1) | AR202364A1 (en, 2012) |
| AT (1) | AT345553B (en, 2012) |
| BE (1) | BE827843A (en, 2012) |
| BR (1) | BR7501990A (en, 2012) |
| CA (1) | CA1057302A (en, 2012) |
| CH (1) | CH606129A5 (en, 2012) |
| DE (1) | DE2514332A1 (en, 2012) |
| DK (1) | DK145782C (en, 2012) |
| FR (1) | FR2267331B1 (en, 2012) |
| GB (1) | GB1494710A (en, 2012) |
| IT (1) | IT1034827B (en, 2012) |
| LU (1) | LU72271A1 (en, 2012) |
| MX (1) | MX147701A (en, 2012) |
| NL (1) | NL7504230A (en, 2012) |
| NO (1) | NO145165C (en, 2012) |
| SE (1) | SE413027B (en, 2012) |
| ZA (1) | ZA751800B (en, 2012) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4104459A (en) * | 1974-08-19 | 1978-08-01 | Ethyl Corporation | Treating polyvinyl chloride resins |
| US4171427A (en) * | 1975-05-16 | 1979-10-16 | Hoechst Aktiengesellschaft | Process for continuously removing monomers from an aqueous dispersion of a polymer |
| DE2526728A1 (de) * | 1975-06-14 | 1976-12-30 | Huels Chemische Werke Ag | Kontinuierliches verfahren zur entfernung von monomeren verunreinigungen aus waessrigen dispersionen von homo- und copolymerisaten des vinylchlorids |
| US4168373A (en) * | 1975-11-24 | 1979-09-18 | Borden, Inc. | Removal of residual vinyl chloride monomer from polyvinyl chloride latex |
| JPS5813563B2 (ja) * | 1976-04-03 | 1983-03-14 | 信越化学工業株式会社 | 塩化ビニルの水性分散液から未反応モノマ−を除去する方法およびその装置 |
| DE2640546C2 (de) * | 1976-09-09 | 1982-07-01 | Hoechst Ag, 6000 Frankfurt | Verfahren zur kontinuierlichen Entfernung von Vinylchlorid aus einer wässerigen Dispersion von Homo- und Copolymerisaten des Vinylchlorids |
| DE2909518A1 (de) * | 1979-03-10 | 1980-09-18 | Bayer Ag | Verfahren zum entfernen von restmonomeren aus abs-polymerisaten |
| US4292424A (en) * | 1980-03-03 | 1981-09-29 | The B.F. Goodrich Company | Process for recovering vinyl polymers from emulsion polymerization latices |
| IT1198338B (it) * | 1980-07-02 | 1988-12-21 | Montedison Spa | Processo per produrre copolimeri di monomeri vinil-aromatici con nitrili etilenicamente insaturi |
| US4461889A (en) * | 1980-09-17 | 1984-07-24 | Phillips Petroleum Company | Separation of solid polymers and liquid diluent |
| JPS5753514A (en) * | 1980-09-17 | 1982-03-30 | Mitsubishi Rayon Co Ltd | Preparation of high-impact resin |
| US4451612A (en) * | 1980-09-22 | 1984-05-29 | Mobil Oil Corporation | Continuous process for the preparation of rubber modified polymers |
| US4408039A (en) * | 1981-08-28 | 1983-10-04 | Phillips Petroleum Company | Separation of polymer of conjugated diene from a solution polymerization solvent using prestripping step |
| DE3580161D1 (de) * | 1984-12-17 | 1990-11-22 | Kanegafuchi Chemical Ind | Verfahren zur entfernung einer organischen verbindung mit hohem siedepunkt. |
| JP2001261751A (ja) * | 2000-03-23 | 2001-09-26 | Kanegafuchi Chem Ind Co Ltd | グラフト共重合体ラテックスの製造方法 |
| KR102068308B1 (ko) | 2016-09-23 | 2020-01-20 | 주식회사 엘지화학 | 고분자의 잔류 모노머 함량 제어방법 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3006872A (en) * | 1957-10-28 | 1961-10-31 | Union Carbide Corp | Coagulation of dispersed polymeric organic material with poly(ethylene oxide), and product thereof |
| US3345430A (en) * | 1962-12-31 | 1967-10-03 | Monsanto Co | Process for recovering graft copolymer latex solids |
| US3248455A (en) * | 1963-08-14 | 1966-04-26 | Us Rubber Co | Method of recovering resinous polymer from latex |
| JPS546269B1 (en, 2012) * | 1970-12-18 | 1979-03-27 | ||
| US3821348A (en) * | 1972-02-25 | 1974-06-28 | Standard Oil Co | Process for recovering nitrile polymer solids from latex |
-
1974
- 1974-04-12 US US05/460,339 patent/US3954910A/en not_active Expired - Lifetime
-
1975
- 1975-03-06 CA CA221,438A patent/CA1057302A/en not_active Expired
- 1975-03-10 SE SE7502671A patent/SE413027B/xx not_active IP Right Cessation
- 1975-03-11 NO NO750813A patent/NO145165C/no unknown
- 1975-03-11 MX MX157077A patent/MX147701A/es unknown
- 1975-03-21 ZA ZA00751800A patent/ZA751800B/xx unknown
- 1975-03-21 GB GB11881/75A patent/GB1494710A/en not_active Expired
- 1975-04-02 DE DE19752514332 patent/DE2514332A1/de not_active Ceased
- 1975-04-03 BR BR2533/75A patent/BR7501990A/pt unknown
- 1975-04-03 IT IT21978/75A patent/IT1034827B/it active
- 1975-04-04 JP JP50041120A patent/JPS6037129B2/ja not_active Expired
- 1975-04-07 DK DK146675A patent/DK145782C/da not_active IP Right Cessation
- 1975-04-07 AR AR258265A patent/AR202364A1/es active
- 1975-04-07 FR FR7510714A patent/FR2267331B1/fr not_active Expired
- 1975-04-09 CH CH452175A patent/CH606129A5/xx not_active IP Right Cessation
- 1975-04-09 NL NL7504230A patent/NL7504230A/xx not_active Application Discontinuation
- 1975-04-09 AT AT268275A patent/AT345553B/de not_active IP Right Cessation
- 1975-04-11 LU LU72271A patent/LU72271A1/xx unknown
- 1975-04-11 BE BE155329A patent/BE827843A/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| AT345553B (de) | 1978-09-25 |
| DK145782C (da) | 1983-08-22 |
| CA1057302A (en) | 1979-06-26 |
| NO145165C (no) | 1982-01-27 |
| DK146675A (en, 2012) | 1975-10-13 |
| NL7504230A (nl) | 1975-10-14 |
| IT1034827B (it) | 1979-10-10 |
| SE7502671L (sv) | 1975-10-13 |
| NO750813L (en, 2012) | 1975-10-14 |
| BR7501990A (pt) | 1976-02-10 |
| AU7961175A (en) | 1976-09-30 |
| FR2267331A1 (en, 2012) | 1975-11-07 |
| FR2267331B1 (en, 2012) | 1978-10-06 |
| ATA268275A (de) | 1978-01-15 |
| NO145165B (no) | 1981-10-19 |
| JPS50136379A (en, 2012) | 1975-10-29 |
| DE2514332A1 (de) | 1975-11-06 |
| US3954910A (en) | 1976-05-04 |
| CH606129A5 (en, 2012) | 1978-10-31 |
| MX147701A (es) | 1983-01-06 |
| LU72271A1 (en, 2012) | 1977-02-03 |
| SE413027B (sv) | 1980-03-31 |
| DK145782B (da) | 1983-02-28 |
| BE827843A (fr) | 1975-10-13 |
| AR202364A1 (es) | 1975-05-30 |
| ZA751800B (en) | 1976-02-25 |
| GB1494710A (en) | 1977-12-14 |
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