DE1083057B - Verfahren zur Herstellung von bestaendigen, fliessfaehigen, polymerisierbaren Gemischen aus monomeren und polymeren Monovinylverbindungen - Google Patents
Verfahren zur Herstellung von bestaendigen, fliessfaehigen, polymerisierbaren Gemischen aus monomeren und polymeren MonovinylverbindungenInfo
- Publication number
- DE1083057B DE1083057B DEP21610A DEP0021610A DE1083057B DE 1083057 B DE1083057 B DE 1083057B DE P21610 A DEP21610 A DE P21610A DE P0021610 A DEP0021610 A DE P0021610A DE 1083057 B DE1083057 B DE 1083057B
- Authority
- DE
- Germany
- Prior art keywords
- polymerization
- viscosity
- syrup
- poise
- monomeric
- 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.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims description 24
- 238000004519 manufacturing process Methods 0.000 title claims description 9
- 239000000203 mixture Substances 0.000 title claims description 8
- 230000009969 flowable effect Effects 0.000 title claims description 6
- 150000001875 compounds Chemical class 0.000 title claims description 5
- 238000006116 polymerization reaction Methods 0.000 claims description 39
- 239000000178 monomer Substances 0.000 claims description 25
- 229920000642 polymer Polymers 0.000 claims description 19
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims description 8
- 239000003431 cross linking reagent Substances 0.000 claims description 6
- 239000012986 chain transfer agent Substances 0.000 claims description 5
- 238000006243 chemical reaction Methods 0.000 claims description 5
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims description 4
- -1 vinyl compound Chemical class 0.000 claims description 4
- 238000001816 cooling Methods 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 239000011541 reaction mixture Substances 0.000 claims description 2
- 229920002554 vinyl polymer Polymers 0.000 claims description 2
- 239000012190 activator Substances 0.000 claims 2
- 239000003381 stabilizer Substances 0.000 claims 2
- 125000005396 acrylic acid ester group Chemical group 0.000 claims 1
- 239000006188 syrup Substances 0.000 description 60
- 235000020357 syrup Nutrition 0.000 description 60
- 244000052769 pathogen Species 0.000 description 26
- 230000001717 pathogenic effect Effects 0.000 description 20
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 15
- 239000003112 inhibitor Substances 0.000 description 8
- 238000003860 storage Methods 0.000 description 6
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 6
- 239000000945 filler Substances 0.000 description 5
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 3
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Chemical compound CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 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
- 239000004342 Benzoyl peroxide Substances 0.000 description 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 235000019400 benzoyl peroxide Nutrition 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000010791 quenching Methods 0.000 description 2
- 230000000171 quenching effect Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000005206 1,2-dihydroxybenzenes Chemical class 0.000 description 1
- BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 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
- JJBFVQSGPLGDNX-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)propyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)COC(=O)C(C)=C JJBFVQSGPLGDNX-UHFFFAOYSA-N 0.000 description 1
- TVWBTVJBDFTVOW-UHFFFAOYSA-N 2-methyl-1-(2-methylpropylperoxy)propane Chemical compound CC(C)COOCC(C)C TVWBTVJBDFTVOW-UHFFFAOYSA-N 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical class CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000007900 aqueous suspension Substances 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
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- RHMZKSWPMYAOAZ-UHFFFAOYSA-N diethyl peroxide Chemical compound CCOOCC RHMZKSWPMYAOAZ-UHFFFAOYSA-N 0.000 description 1
- 231100000676 disease causative agent Toxicity 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 125000003438 dodecyl group Chemical group [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])* 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000011152 fibreglass Substances 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 239000002990 reinforced plastic Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000013022 venting Methods 0.000 description 1
- 238000005406 washing Methods 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
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
-
- 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
- C08F2/02—Polymerisation in bulk
-
- 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
- C08F2/38—Polymerisation using regulators, e.g. chain terminating agents, e.g. telomerisation
-
- 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
- C08F2/38—Polymerisation using regulators, e.g. chain terminating agents, e.g. telomerisation
- C08F2/42—Polymerisation using regulators, e.g. chain terminating agents, e.g. telomerisation using short-stopping agents
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/10—Esters
- C08F20/12—Esters of monohydric alcohols or phenols
- C08F20/14—Methyl esters, e.g. methyl (meth)acrylate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Polymerization Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US69451357A | 1957-11-05 | 1957-11-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1083057B true DE1083057B (de) | 1960-06-09 |
Family
ID=24789132
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEP21610A Pending DE1083057B (de) | 1957-11-05 | 1958-10-28 | Verfahren zur Herstellung von bestaendigen, fliessfaehigen, polymerisierbaren Gemischen aus monomeren und polymeren Monovinylverbindungen |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3380980A (en:Method) |
| BE (1) | BE572359A (en:Method) |
| CH (1) | CH414151A (en:Method) |
| DE (1) | DE1083057B (en:Method) |
| FR (1) | FR1214272A (en:Method) |
| GB (1) | GB870191A (en:Method) |
| NL (2) | NL111822C (en:Method) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3290410A (en) * | 1961-06-06 | 1966-12-06 | Degussa | Cold curing reaction lacquers containing at least one component containing ethylenicunsaturation curable by polymerization |
| DE2327722A1 (de) * | 1972-06-02 | 1973-12-20 | Ici Ltd | Verfahren zur herstellung von acrylplatten |
| EP0004851A3 (en) * | 1978-04-22 | 1979-11-28 | Rohm Gmbh | Process for the partial polymerisation of vinyl monomers and use of the polymer syrups obtained |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH465213A (de) * | 1965-05-14 | 1968-11-15 | Glidden Durkee Division Scm Co | Bei niedriger Temperatur und an der Luft polymerisierbare Masse sowie Verwendung derselben zur Herstellung von Formkörpern |
| NL124155C (en:Method) * | 1965-07-23 | |||
| FR1473094A (fr) * | 1966-01-06 | 1967-03-17 | Electrochimie Soc | Procédé de polymérisation des esters acryliques et méthacryliques |
| US3726586A (en) * | 1970-12-18 | 1973-04-10 | Rohm & Haas | Wedge shaped optical body |
| US4113803A (en) | 1972-06-02 | 1978-09-12 | Imperial Chemical Industries Limited | Acrylic sheet having improved thermoshaping properties |
| JPS5236154B2 (en:Method) * | 1973-01-18 | 1977-09-13 | ||
| GB1410697A (en) | 1973-10-26 | 1975-10-22 | Ucb Sa | Olefinically-usaturated organic polymers |
| US4312726A (en) | 1973-10-26 | 1982-01-26 | Ucb, Societe Anonyme | Semi-telechelic olefinically-unsaturated organic polymers |
| US4148949A (en) * | 1976-02-02 | 1979-04-10 | Weyerhaeuser Company | Method of increasing polymerization reaction rates in the production of a fiber-thermoplastic matrix by in situ bulk polymerization |
| US4239875A (en) | 1977-01-24 | 1980-12-16 | Etlis Volf S | Method for producing prepolymers based on vinyl monomers |
| DE2711478A1 (de) * | 1977-03-16 | 1978-09-21 | Arledter Hanns F | Verfahren zur thermischen polymerisation, polykondensation oder kondensation von monomeren kunststoffen in poroesen werkstoffen |
| US4152506A (en) * | 1978-04-26 | 1979-05-01 | E. I. Du Pont De Nemours And Company | Preparation of thermoformable methyl methacrylate sheets |
| US4328329A (en) * | 1980-12-11 | 1982-05-04 | E. I. Du Pont De Nemours And Company | Process for polymerizing methyl methacrylate syrup using a dual initiator system |
| DE3207263A1 (de) * | 1982-03-01 | 1983-09-08 | Henkel KGaA, 4000 Düsseldorf | Organo-borverbindungen enthaltende stoffgemische, verfahren zu ihrer herstellung und ihre verwendung |
| US4622377A (en) * | 1984-09-20 | 1986-11-11 | Swedlow, Inc. | Plastic transparency and method for making it |
| FR2590563B1 (fr) * | 1985-11-22 | 1992-02-21 | Charbonnages Ste Chimique | Fluidifiant pour mortiers a base de liants organiques et mortiers ainsi obtenus |
| FR2625569B1 (fr) * | 1987-12-30 | 1990-05-04 | Charbonnages Ste Chimique | Procede de preparation d'optiques organiques |
| FR2625570B1 (fr) * | 1987-12-30 | 1990-05-04 | Charbonnages Ste Chimique | Procede de preparation d'optiques organiques a saut(s) d'indice |
| US5344902A (en) * | 1991-06-18 | 1994-09-06 | Occidental Research Corporation | Polymerization with initiator and quaternary ammonium salt |
| US5264530A (en) * | 1992-05-01 | 1993-11-23 | E. I. Du Pont De Nemours And Company | Process of polymerization in an aqueous system |
| US5643994A (en) * | 1994-09-21 | 1997-07-01 | Illinois Tool Works Inc. | Anchoring systems and methods utilizing acrylate compositions |
| US5965635A (en) * | 1995-06-07 | 1999-10-12 | Illinois Tool Works Inc. | Alkylacrylate ester composition for anchoring materials in or to concrete or masonry |
| DE10349544A1 (de) * | 2003-10-22 | 2005-05-25 | Röhm GmbH & Co. KG | Herstellung von farblosen, transparent oder gedeckt eingefärbten PLEXIGLAS-Blöcken aus restinitiatorfreiem Präpolymerisat durch thermische Polymerisation |
| US8642676B2 (en) * | 2009-09-15 | 2014-02-04 | Mitsubishi Rayon Co., Ltd. | Polymerizable composition and acrylic resin film |
| FR2981652B1 (fr) * | 2011-10-21 | 2015-03-27 | Arkema France | Composites via la polymerisation in-situ de resines thermoplastiques methacryliques |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2462895A (en) * | 1945-01-30 | 1949-03-01 | Du Pont | Preparation of modified polymeric methyl methacrylate |
| US2471959A (en) * | 1948-01-15 | 1949-05-31 | Du Pont | Polymerizations employing azo compounds as catalysts |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2120006A (en) * | 1935-04-26 | 1938-06-07 | Du Pont | Molding organic compounds |
| US2116318A (en) * | 1935-07-31 | 1938-05-03 | Du Pont | Electrical equipment |
| US2482825A (en) * | 1946-07-05 | 1949-09-27 | Dow Chemical Co | Putty comprising a liquid monomer and a finely divided solid insoluble polymer |
-
0
- NL NL232891D patent/NL232891A/xx unknown
- BE BE572359D patent/BE572359A/xx unknown
- NL NL111822D patent/NL111822C/xx active
-
1958
- 1958-10-24 FR FR1214272D patent/FR1214272A/fr not_active Expired
- 1958-10-28 DE DEP21610A patent/DE1083057B/de active Pending
- 1958-11-04 GB GB35322/58A patent/GB870191A/en not_active Expired
- 1958-11-05 CH CH6582658A patent/CH414151A/de unknown
-
1965
- 1965-01-06 US US423849A patent/US3380980A/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2462895A (en) * | 1945-01-30 | 1949-03-01 | Du Pont | Preparation of modified polymeric methyl methacrylate |
| US2471959A (en) * | 1948-01-15 | 1949-05-31 | Du Pont | Polymerizations employing azo compounds as catalysts |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3290410A (en) * | 1961-06-06 | 1966-12-06 | Degussa | Cold curing reaction lacquers containing at least one component containing ethylenicunsaturation curable by polymerization |
| DE2327722A1 (de) * | 1972-06-02 | 1973-12-20 | Ici Ltd | Verfahren zur herstellung von acrylplatten |
| EP0004851A3 (en) * | 1978-04-22 | 1979-11-28 | Rohm Gmbh | Process for the partial polymerisation of vinyl monomers and use of the polymer syrups obtained |
| US4224425A (en) * | 1978-04-22 | 1980-09-23 | Rohm Gmbh | Partial polymerization method for vinyl monomers |
Also Published As
| Publication number | Publication date |
|---|---|
| US3380980A (en) | 1968-04-30 |
| NL232891A (en:Method) | |
| NL111822C (en:Method) | |
| FR1214272A (fr) | 1960-04-07 |
| GB870191A (en) | 1961-06-14 |
| CH414151A (de) | 1966-05-31 |
| BE572359A (en:Method) |
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