NL8501008A - Werkwijze voor het behandelen van een emulsie van een of meer monomeren. - Google Patents

Werkwijze voor het behandelen van een emulsie van een of meer monomeren. Download PDF

Info

Publication number: NL8501008A
Authority: NL; Netherlands
Prior art keywords: emulsion; weight; ethylenically unsaturated; free radical; monomers
Prior art date: 1984-04-10

Application number

NL8501008A

Other languages

English (en)

Dutch (nl)

Original Assignee

Polysar Ltd

Priority date (The priority date 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 date listed.)

1984-04-10

Filing date

1985-04-04

Publication date

1985-11-01

1985-04-04 Application filed by Polysar Ltd filed Critical Polysar Ltd

1985-11-01 Publication of NL8501008A publication Critical patent/NL8501008A/nl

Links

239000000178 monomer Substances 0.000 title claims description 45
238000000034 method Methods 0.000 title claims description 35
239000000839 emulsion Substances 0.000 title claims description 21
150000003254 radicals Chemical class 0.000 claims description 33
229920000642 polymer Polymers 0.000 claims description 19
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical group OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 10
239000002253 acid Chemical class 0.000 claims description 10
125000000217 alkyl group Chemical group 0.000 claims description 10
239000003638 chemical reducing agent Substances 0.000 claims description 9
150000001735 carboxylic acids Chemical class 0.000 claims description 7
-1 alkyl peroxide Chemical class 0.000 claims description 6
229920002554 vinyl polymer Polymers 0.000 claims description 6
150000007513 acids Chemical class 0.000 claims description 5
230000015556 catabolic process Effects 0.000 claims description 5
238000006731 degradation reaction Methods 0.000 claims description 5
150000002148 esters Chemical class 0.000 claims description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
150000001299 aldehydes Chemical class 0.000 claims description 4
125000003342 alkenyl group Chemical group 0.000 claims description 4
150000001408 amides Chemical class 0.000 claims description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 4
150000001993 dienes Chemical class 0.000 claims description 4
150000002825 nitriles Chemical class 0.000 claims description 4
238000010992 reflux Methods 0.000 claims description 4
HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical group [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 claims description 4
229940001584 sodium metabisulfite Drugs 0.000 claims description 4
235000010262 sodium metabisulphite Nutrition 0.000 claims description 4
235000000346 sugar Nutrition 0.000 claims description 4
150000008163 sugars Chemical class 0.000 claims description 4
230000001687 destabilization Effects 0.000 claims description 3
150000002432 hydroperoxides Chemical class 0.000 claims description 3
150000001451 organic peroxides Chemical group 0.000 claims description 3
239000007800 oxidant agent Substances 0.000 claims description 3
229920006395 saturated elastomer Polymers 0.000 claims description 3
150000003464 sulfur compounds Chemical class 0.000 claims description 3
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 3
OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 claims description 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 2
239000000460 chlorine Substances 0.000 claims description 2
229910052801 chlorine Inorganic materials 0.000 claims description 2
150000008049 diazo compounds Chemical class 0.000 claims description 2
229910052757 nitrogen Inorganic materials 0.000 claims description 2
125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
150000003623 transition metal compounds Chemical class 0.000 claims description 2
125000004429 atom Chemical group 0.000 claims 1
229920000126 latex Polymers 0.000 description 31
239000004816 latex Substances 0.000 description 29
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 6
239000000203 mixture Substances 0.000 description 6
239000000126 substance Substances 0.000 description 5
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 4
229910052784 alkaline earth metal Inorganic materials 0.000 description 4
JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 3
238000010793 Steam injection (oil industry) Methods 0.000 description 3
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 3
238000009835 boiling Methods 0.000 description 3
MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
150000002978 peroxides Chemical class 0.000 description 3
125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 3
CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 3
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
239000004215 Carbon black (E152) Substances 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
239000005977 Ethylene Substances 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
239000002174 Styrene-butadiene Substances 0.000 description 2
239000003513 alkali Substances 0.000 description 2
239000012530 fluid Substances 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
150000002430 hydrocarbons Chemical class 0.000 description 2
PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000011115 styrene butadiene Substances 0.000 description 2
229920003048 styrene butadiene rubber Polymers 0.000 description 2
WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
SBYMUDUGTIKLCR-UHFFFAOYSA-N 2-chloroethenylbenzene Chemical compound ClC=CC1=CC=CC=C1 SBYMUDUGTIKLCR-UHFFFAOYSA-N 0.000 description 1
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
239000004342 Benzoyl peroxide Substances 0.000 description 1
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
OCUCCJIRFHNWBP-IYEMJOQQSA-L Copper gluconate Chemical class [Cu+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O OCUCCJIRFHNWBP-IYEMJOQQSA-L 0.000 description 1
FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
PMVSDNDAUGGCCE-TYYBGVCCSA-L Ferrous fumarate Chemical compound [Fe+2].[O-]C(=O)\C=C\C([O-])=O PMVSDNDAUGGCCE-TYYBGVCCSA-L 0.000 description 1
229930195725 Mannitol Natural products 0.000 description 1
STNJBCKSHOAVAJ-UHFFFAOYSA-N Methacrolein Chemical compound CC(=C)C=O STNJBCKSHOAVAJ-UHFFFAOYSA-N 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
YMOONIIMQBGTDU-VOTSOKGWSA-N [(e)-2-bromoethenyl]benzene Chemical compound Br\C=C\C1=CC=CC=C1 YMOONIIMQBGTDU-VOTSOKGWSA-N 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
239000000908 ammonium hydroxide Substances 0.000 description 1
125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
238000003889 chemical engineering Methods 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
229930016911 cinnamic acid Natural products 0.000 description 1
235000013985 cinnamic acid Nutrition 0.000 description 1
150000001868 cobalt Chemical class 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
230000000368 destabilizing effect Effects 0.000 description 1
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
WBZKQQHYRPRKNJ-UHFFFAOYSA-L disulfite Chemical compound [O-]S(=O)S([O-])(=O)=O WBZKQQHYRPRKNJ-UHFFFAOYSA-L 0.000 description 1
238000007720 emulsion polymerization reaction Methods 0.000 description 1
238000005265 energy consumption Methods 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
239000005038 ethylene vinyl acetate Substances 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
238000005187 foaming Methods 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
235000010355 mannitol Nutrition 0.000 description 1
239000000594 mannitol Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 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
DNTMQTKDNSEIFO-UHFFFAOYSA-N n-(hydroxymethyl)-2-methylprop-2-enamide Chemical compound CC(=C)C(=O)NCO DNTMQTKDNSEIFO-UHFFFAOYSA-N 0.000 description 1
KCAMXZBMXVIIQN-UHFFFAOYSA-N octan-3-yl 2-methylprop-2-enoate Chemical compound CCCCCC(CC)OC(=O)C(C)=C KCAMXZBMXVIIQN-UHFFFAOYSA-N 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
229920002587 poly(1,3-butadiene) polymer Polymers 0.000 description 1
229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
150000003573 thiols Chemical class 0.000 description 1
229920001567 vinyl ester resin Polymers 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
- C08F6/006—Removal of residual monomers by chemical reaction, e.g. scavenging
- 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
- C08F6/001—Removal of residual monomers by physical means
- C08F6/003—Removal of residual monomers by physical means from polymer solutions, suspensions, dispersions or emulsions without recovery of the polymer therefrom

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
General Chemical & Material Sciences (AREA)
Dispersion Chemistry (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

NL8501008A 1984-04-10 1985-04-04 Werkwijze voor het behandelen van een emulsie van een of meer monomeren. NL8501008A (nl)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US06/598,927 US4529753A (en)	1984-04-10	1984-04-10	Chemical/steam stripping
US59892784		1984-04-10

Publications (1)

Publication Number	Publication Date
NL8501008A true NL8501008A (nl)	1985-11-01

Family

ID=24397507

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL8501008A NL8501008A (nl)	1984-04-10	1985-04-04	Werkwijze voor het behandelen van een emulsie van een of meer monomeren.

Country Status (10)

Country	Link
US (1)	US4529753A (de)
EP (1)	EP0158523B2 (de)
JP (1)	JPS60229902A (de)
AU (1)	AU577363B2 (de)
BR (1)	BR8501656A (de)
CA (1)	CA1229947A (de)
DE (1)	DE3565682D1 (de)
FI (1)	FI82062C (de)
FR (1)	FR2562545B1 (de)
NL (1)	NL8501008A (de)

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US4737577A (en) *	1986-12-31	1988-04-12	Minnesota Mining And Manufacturing Company	Method for removing monomer from an acrylate adhesive by reaction with a scavenger monomer
US4687807A (en) *	1987-02-13	1987-08-18	Nalco Chemical Company	Use of amidase for reducing the acrylamide content of water-in-oil emulsions containing acrylamide polymers
JPS63260907A (ja) *	1987-04-17	1988-10-27	Mitsubishi Petrochem Co Ltd	高吸水性ポリマ−の製造法
DE3724709A1 (de) *	1987-07-25	1989-02-02	Stockhausen Chem Fab Gmbh	Verfahren zur herstellung von polymerisaten mit niedrigem restmonomergehalt
DE4110058A1 (de) *	1991-03-27	1992-10-01	Hoechst Ag	Verfahren zur verminderung des restmonomerengehaltes in waessrigen kunststoffdispersionen auf polyvinylesterbasis
US5430127A (en) *	1993-11-02	1995-07-04	National Starch And Chemical Investment Holding Corporation	Process for minimizing residual monomers
US5506318A (en) *	1993-12-13	1996-04-09	Air Products And Chemicals, Inc.	Process for producing N-vinyl pyrrolidone polymer having low residual monomer
CN1120180C (zh) *	1994-06-03	2003-09-03	巴斯福股份公司	聚合物水分散液的制备
DE4435422A1 (de) *	1994-10-04	1996-04-18	Basf Ag	Verfahren zur Herstellung einer wäßrigen Polymerisatdispersion
US5459215A (en) *	1995-01-03	1995-10-17	Lucky Ltd.	Process for producing a heat-resistant copolymer
DE19741184A1 (de)	1997-09-18	1999-03-25	Basf Ag	Verfahren zur Verminderung von Restmonomeren in Flüssigsystemen unter Zugabe eines Redoxinitiatorsystems
DE19828183A1 (de) *	1998-06-24	1999-12-30	Basf Ag	Verfahren zur Entfernung von restflüchtigen Komponenten aus Polymerdispersionen
DE19839199A1 (de)	1998-08-28	2000-03-02	Basf Ag	Verfahren zur Verminderung der Restmonomerenmenge in wässrigen Polymerdispersionen
DE19840586A1 (de)	1998-09-05	2000-03-09	Basf Ag	Verfahren zur Verminderung der Restmonomerenmenge in wässrigen Polymerdispersionen
DE19853421A1 (de) *	1998-11-19	2000-05-25	Wacker Chemie Gmbh	Verfahren zur Minderung der Geruchsemission wässriger Schutzkolloid-stabilisierter Vinylaromat-1,3-Dien-Copolymerisat-dispersionen
DE19911170A1 (de)	1999-03-12	2000-09-14	Basf Ag	Verfahren zum Herstellen von W/O-Emulsionen
DE19928934A1 (de)	1999-06-24	2000-12-28	Wacker Polymer Systems Gmbh	Verfahren zur Minderung der Geruchsemission wässriger Vinylaromat-1,3-Dien-Copolymerisatdispersionen
DE10227589A1 (de)	2002-06-20	2004-01-15	Wacker Polymer Systems Gmbh & Co. Kg	Verfahren zur Verringerung der Geruchsemission in wässrigen Polymerdispersionen und in Polymerpulvern
DE10317434A1 (de) *	2003-04-15	2004-10-28	Basf Ag	Verfahren zur Reduzierung der Restmonomerenmenge in wässrigen Polymerdispersionen
DE10335958A1 (de) *	2003-08-04	2005-02-24	Basf Ag	Verfahren zur Herstellung wässriger Polymerisatdispersionen
DE102004002650A1 (de) *	2004-01-16	2005-08-11	Basf Ag	Acrylat-Polymerisate auf Basis von tert.-Butylacrylat zur Verwendung in Sprayformulierungen
KR100684425B1 (ko) *	2004-10-21	2007-02-16	주식회사 엘지화학	스티렌-부타디엔계 라텍스의 제조방법
DE502006003213D1 (de) *	2005-10-07	2009-04-30	Basf Se	Haarfestiger auf basis von t-butylacrylat und hydroxyalkylmethacrylat
EP2501731B1 (de)	2009-11-16	2013-10-23	DSM IP Assets B.V.	Acrylpolymer
US8211987B2 (en)	2010-04-13	2012-07-03	Basf Se	Deodorization of polymer compositions
EP2558507A1 (de)	2010-04-13	2013-02-20	Basf Se	Desodorierung von polymerzusammensetzungen
CN103237825B (zh)	2010-12-02	2015-10-07	帝斯曼知识产权资产管理有限公司	丙烯酸类聚合物
WO2014161817A1 (de)	2013-04-03	2014-10-09	Basf Se	Verfahren zur reduzierung der restmonomerenmenge in einer wässrigen polymerisatdispersion
EP2965785A1 (de)	2014-07-11	2016-01-13	DSM IP Assets B.V.	Neuartige Verwendung
CN111491964A (zh)	2017-12-22	2020-08-04	帝斯曼知识产权资产管理有限公司	粘合剂组合物及其在3d打印中的用途
US12281071B2 (en)	2022-07-22	2025-04-22	T.En Process Technology, Inc.	Systems and methods for enhancing the recovery of styrene

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US3583967A (en) *	1968-12-06	1971-06-08	Kao Corp	Method for obtaining polymer from polymer solution
US3534009A (en) *	1969-01-29	1970-10-13	Du Pont	Method for reducing residual vinyl acetate monomer
JPS5111878A (en) *	1974-07-19	1976-01-30	Kureha Chemical Ind Co Ltd	Ratetsukusuyori mihannomonomaano jokyohoho
NO752264L (de) *	1974-08-29	1976-03-02	Huels Chemische Werke Ag
DD132588A1 (de) *	1977-08-11	1978-10-11	Dirk Wulff	Verfahren zur herstellung von vinylchloridpolymeren mit geringem rest-vinylchloridgehalt
JPS5437988A (en) *	1977-08-31	1979-03-20	Komatsu Ltd	Method and apparatus of grinding a crank shaft
US4251412A (en) *	1978-11-01	1981-02-17	The B. F. Goodrich Company	Reducing residual acrylonitrile in water dispersions of acrylonitrile polymers with amine
US4272425A (en) *	1979-10-26	1981-06-09	The B. F. Goodrich Company	Treating dispersions of acrylonitrile polymers
DE3006172A1 (de) *	1980-02-19	1981-08-20	Röhm GmbH, 6100 Darmstadt	Verfahren zur herstellung rest-acrylnitril-armer polymerisat-dispersionen
US4278582A (en) *	1980-02-25	1981-07-14	The B. F. Goodrich Company	Removal of residual acrylonitrile monomer

1984
- 1984-04-10 US US06/598,927 patent/US4529753A/en not_active Expired - Fee Related
1985
- 1985-03-14 CA CA000476520A patent/CA1229947A/en not_active Expired
- 1985-04-04 AU AU40880/85A patent/AU577363B2/en not_active Ceased
- 1985-04-04 NL NL8501008A patent/NL8501008A/nl active Search and Examination
- 1985-04-04 EP EP85302414A patent/EP0158523B2/de not_active Expired
- 1985-04-04 DE DE8585302414T patent/DE3565682D1/de not_active Expired
- 1985-04-05 FR FR8505276A patent/FR2562545B1/fr not_active Expired
- 1985-04-09 BR BR8501656A patent/BR8501656A/pt not_active IP Right Cessation
- 1985-04-09 FI FI851399A patent/FI82062C/fi not_active IP Right Cessation
- 1985-04-09 JP JP60075249A patent/JPS60229902A/ja active Granted

Also Published As

Publication number	Publication date
EP0158523A3 (en)	1986-03-19
FI82062C (fi)	1991-01-10
FR2562545B1 (fr)	1987-07-10
FI82062B (fi)	1990-09-28
DE3565682D1 (en)	1988-11-24
JPH0344561B2 (de)	1991-07-08
BR8501656A (pt)	1985-12-10
FI851399A0 (fi)	1985-04-09
EP0158523B1 (de)	1988-10-19
CA1229947A (en)	1987-12-01
JPS60229902A (ja)	1985-11-15
FR2562545A1 (fr)	1985-10-11
US4529753A (en)	1985-07-16
AU577363B2 (en)	1988-09-22
EP0158523A2 (de)	1985-10-16
FI851399L (fi)	1985-10-11
AU4088085A (en)	1985-10-17
EP0158523B2 (de)	1992-11-25

Legal Events

Date	Code	Title	Description
1989-06-01	BA	A request for search or an international-type search has been filed
1989-07-03	BB	A search report has been drawn up
1989-07-16	CNR	Transfer of rights (patent application after its laying open for public inspection)	Free format text: BASF AKTIENGESELLSCHAFT
1990-02-01	BC	A request for examination has been filed
1993-05-03	BN	A decision not to publish the application has become irrevocable

Publication	Publication Date	Title
NL8501008A (nl)	1985-11-01	Werkwijze voor het behandelen van een emulsie van een of meer monomeren.
EP0113830B1 (de)	1987-02-04	Entfernung von rückständigem Acrylonitrilmonomer
CA1160382A (en)	1984-01-10	Treating dispersions of acrylonitrile polymers
US4251412A (en)	1981-02-17	Reducing residual acrylonitrile in water dispersions of acrylonitrile polymers with amine
JPH0145486B2 (de)	1989-10-03
US2451180A (en)	1948-10-12	Catalysts for the polymerization of butadiene-1,3 hydrocarbons
US3069382A (en)	1962-12-18	Reduction of water-soluble peroxides in a graft copolymerization process
EP0000419A1 (de)	1979-01-24	Verfahren zur Herstellung von Copolymeren und die ganz oder teilweise aus diesen Copolymeren hergestellten Produkte.
US4117240A (en)	1978-09-26	Stabilized polymeric compositions
US4255307A (en)	1981-03-10	Reducing residual acrylonitrile in water dispersions of acrylonitrile polymers with alkali or ammonium sulfite
JPS6157435B2 (de)	1986-12-06
US2483778A (en)	1949-10-04	Inhibition of resin growth from diolefins
US2417034A (en)	1947-03-04	Butadiene emulsion polymerization in the presence of water soluble complex metal cyanides
JPS6123805B2 (de)	1986-06-07
WO1998051714A1 (en)	1998-11-19	N-ethylhydroxylamine as a shortstopping agent for free radical polymerization
GB1597920A (en)	1981-09-16	Manufacture of polymers in bead form from water-soluble ethylenically unsaturated monomers
JPS61266417A (ja)	1986-11-26	水媒体中の遊離残留単量体の除去方法
JP3128741B2 (ja)	2001-01-29	共重合体ラテックスの製造方法
GB1583269A (en)	1981-01-21	Manufacture of polymers in bead form from one or more water-soluble ethylenically unsaturated monomers
US3882069A (en)	1975-05-06	Stabilized dispersions of chloroprene polymers
CN85101585A (zh)	1985-12-20	化学的/蒸汽汽提
DE69201884T2 (de)	1995-09-21	Zusammensetzung zur Verhinderung von Inkrustierungen in Polymerisationsreaktoren und Methode für die Polymerisation von Vinyl-Monomeren mit derselben.
JP3178039B2 (ja)	2001-06-18	８−オキシキノリンのスルフィド化合物からなる重合器内部表面の付着防止剤及び該付着防止剤を用いたビニル系単量体の重合方法
US3328370A (en)	1967-06-27	Process for the manufacture of polychloroprene rubber
US2380554A (en)	1945-07-31	Polymerization in aqueous emulsion