DE1175431B - Stabilisieren von Acrylnitrilpolymerisaten - Google Patents
Stabilisieren von AcrylnitrilpolymerisatenInfo
- Publication number
- DE1175431B DE1175431B DEF34511A DEF0034511A DE1175431B DE 1175431 B DE1175431 B DE 1175431B DE F34511 A DEF34511 A DE F34511A DE F0034511 A DEF0034511 A DE F0034511A DE 1175431 B DE1175431 B DE 1175431B
- Authority
- DE
- Germany
- Prior art keywords
- solutions
- acrylonitrile
- polymer
- yellowing
- stabilizers
- 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
- 229920002239 polyacrylonitrile Polymers 0.000 title claims description 16
- 230000006641 stabilisation Effects 0.000 title 1
- 238000011105 stabilization Methods 0.000 title 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 6
- UYHCMAZIKNVDSX-POHAHGRESA-N [(z)-benzylideneamino]thiourea Chemical compound NC(=S)N\N=C/C1=CC=CC=C1 UYHCMAZIKNVDSX-POHAHGRESA-N 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 claims 2
- 238000004513 sizing Methods 0.000 claims 1
- 239000000243 solution Substances 0.000 description 29
- 239000003381 stabilizer Substances 0.000 description 22
- 229920000642 polymer Polymers 0.000 description 16
- 238000004383 yellowing Methods 0.000 description 13
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
- 238000000034 method Methods 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 4
- JMULZUQMMLAALR-YRNVUSSQSA-N [(e)-1-phenylethylideneamino]thiourea Chemical compound NC(=S)N\N=C(/C)C1=CC=CC=C1 JMULZUQMMLAALR-YRNVUSSQSA-N 0.000 description 3
- 238000002835 absorbance Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 238000004090 dissolution Methods 0.000 description 3
- 229920000915 polyvinyl chloride Polymers 0.000 description 3
- 239000004800 polyvinyl chloride Substances 0.000 description 3
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000008033 biological extinction Effects 0.000 description 2
- FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 2
- 229940042396 direct acting antivirals thiosemicarbazones Drugs 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000007669 thermal treatment Methods 0.000 description 2
- 150000003584 thiosemicarbazones Chemical class 0.000 description 2
- GYRDZVHNPFBIST-UHFFFAOYSA-N (cyclohexylideneamino)thiourea Chemical compound NC(=S)NN=C1CCCCC1 GYRDZVHNPFBIST-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
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical class NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-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
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- SHUQFXIRXYXNOZ-JHLWKMQHSA-N [(z)-[(e)-3-phenylprop-2-enylidene]amino]thiourea Chemical compound NC(=S)N\N=C/C=C/C1=CC=CC=C1 SHUQFXIRXYXNOZ-JHLWKMQHSA-N 0.000 description 1
- 239000000370 acceptor Substances 0.000 description 1
- FQUDPIIGGVBZEQ-UHFFFAOYSA-N acetone thiosemicarbazone Chemical compound CC(C)=NNC(N)=S FQUDPIIGGVBZEQ-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- OHNSRYBTSVDDKA-BJMVGYQFSA-N chembl242112 Chemical compound NC(=S)N\N=C\C1=CC=CC=C1O OHNSRYBTSVDDKA-BJMVGYQFSA-N 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical class CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003583 thiosemicarbazides Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/17—Amines; Quaternary ammonium compounds
- C08K5/175—Amines; Quaternary ammonium compounds containing COOH-groups; Esters or salts thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/39—Thiocarbamic acids; Derivatives thereof, e.g. dithiocarbamates
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Pyrrole Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (13)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL280590D NL280590A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1961-07-07 | ||
BE619857D BE619857A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1961-07-07 | ||
DEF34511A DE1175431B (de) | 1961-07-07 | 1961-07-22 | Stabilisieren von Acrylnitrilpolymerisaten |
DEF34510A DE1162557B (de) | 1961-07-07 | 1961-07-22 | Verfahren zum Stabilisieren von Loesungen des Polyacrylnitrils |
DEF35104A DE1179365B (de) | 1961-07-07 | 1961-10-10 | Verfahren zum Stabilisieren von Acrylnitril-polymerisat-Loesungen |
DEF35105A DE1179366B (de) | 1961-07-07 | 1961-10-10 | Verfahren zur Herstellung stabilisierter Acrylnitrilpolymerisat-Loesungen |
CH704562A CH469035A (de) | 1961-07-07 | 1962-06-12 | Verfahren zur Stabilisierung von Acrylnitril-Polymerisat-Lösungen |
US204626A US3314914A (en) | 1961-07-07 | 1962-06-22 | Process for the production of stabilized acrylonitrile polymer solutions |
FI621254A FI42475C (fi) | 1961-07-07 | 1962-06-29 | Tapa stabiloida akryylinitriilipolymeeriliuoksia |
GB25679/62A GB960520A (en) | 1961-07-07 | 1962-07-04 | A process for the production of stabilised acrylonitrile polymer solutions |
FR902889A FR1331004A (fr) | 1961-07-07 | 1962-07-04 | Procédé de préparation de solutions stabilisées de polymères d'acrylonitrile |
DK303662AA DK106247C (da) | 1961-07-07 | 1962-07-06 | Fremgangsmåde til stabilisering af acrylonitrilpolymerisatopløsninger mod misfarvning. |
SE7615/62A SE303875B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1961-07-07 | 1962-07-06 |
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEF0034378 | 1961-07-07 | ||
DEF34510A DE1162557B (de) | 1961-07-07 | 1961-07-22 | Verfahren zum Stabilisieren von Loesungen des Polyacrylnitrils |
DEF34511A DE1175431B (de) | 1961-07-07 | 1961-07-22 | Stabilisieren von Acrylnitrilpolymerisaten |
DEF35104A DE1179365B (de) | 1961-07-07 | 1961-10-10 | Verfahren zum Stabilisieren von Acrylnitril-polymerisat-Loesungen |
DEF35105A DE1179366B (de) | 1961-07-07 | 1961-10-10 | Verfahren zur Herstellung stabilisierter Acrylnitrilpolymerisat-Loesungen |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1175431B true DE1175431B (de) | 1964-08-06 |
Family
ID=27512035
Family Applications (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEF34511A Pending DE1175431B (de) | 1961-07-07 | 1961-07-22 | Stabilisieren von Acrylnitrilpolymerisaten |
DEF34510A Pending DE1162557B (de) | 1961-07-07 | 1961-07-22 | Verfahren zum Stabilisieren von Loesungen des Polyacrylnitrils |
DEF35104A Pending DE1179365B (de) | 1961-07-07 | 1961-10-10 | Verfahren zum Stabilisieren von Acrylnitril-polymerisat-Loesungen |
DEF35105A Pending DE1179366B (de) | 1961-07-07 | 1961-10-10 | Verfahren zur Herstellung stabilisierter Acrylnitrilpolymerisat-Loesungen |
Family Applications After (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEF34510A Pending DE1162557B (de) | 1961-07-07 | 1961-07-22 | Verfahren zum Stabilisieren von Loesungen des Polyacrylnitrils |
DEF35104A Pending DE1179365B (de) | 1961-07-07 | 1961-10-10 | Verfahren zum Stabilisieren von Acrylnitril-polymerisat-Loesungen |
DEF35105A Pending DE1179366B (de) | 1961-07-07 | 1961-10-10 | Verfahren zur Herstellung stabilisierter Acrylnitrilpolymerisat-Loesungen |
Country Status (9)
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3419659A (en) * | 1964-07-08 | 1968-12-31 | Gaf Corp | Sun screening methods |
US3484508A (en) * | 1967-05-03 | 1969-12-16 | Ibm | Process of making spongeous transfer medium for moderate impact applications |
US3925305A (en) * | 1973-08-08 | 1975-12-09 | Standard Oil Co Ohio | Thermally-stable high nitrile resins and method for producing the same |
US4151151A (en) * | 1978-01-16 | 1979-04-24 | The Standard Oil Company | Flow improvers for high nitrile copolymers |
DE102006011933B4 (de) * | 2006-03-15 | 2010-04-15 | Baerlocher Gmbh | Stabilisatorzusammensetzungen für halogenhaltige Polymere mit verbesserter Anfangsfarbe und verbesserter Farbhaltung, diese enthaltende Polymerzusammensetzungen und Formkörper sowie Verfahren zur Stabilisierung halogenhaltiger Polymere |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2821519A (en) * | 1955-12-30 | 1958-01-28 | Gen Aniline & Film Corp | Stabilization of polymeric n-vinyl pyrrolidones with hydrazino compounds |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2396156A (en) * | 1942-08-12 | 1946-03-05 | Du Pont | Stabilization of organic substances |
US2353690A (en) * | 1942-11-11 | 1944-07-18 | Du Pont | Stabilization of organic substances |
US2614090A (en) * | 1949-08-15 | 1952-10-14 | Goodrich Co B F | Stabilization of vinylidene cyanide polymer solutions |
US2661347A (en) * | 1950-10-26 | 1953-12-01 | Monsanto Chemicals | Stabilized acrylonitrile polymers |
US2681329A (en) * | 1952-09-04 | 1954-06-15 | Dow Chemical Co | Acrylonitrile polymers stabilized with certain nu-alkyl hydroxyacetamides |
US2775574A (en) * | 1953-04-27 | 1956-12-25 | Monsanto Chemicals | Acrylonitrile copolymers stabilized with cinnamic acid and its salts |
US2878208A (en) * | 1956-05-23 | 1959-03-17 | Chemstrand Corp | Acrylonitrile polymer composition stabilized with formaldehyde, ethylenediamine tetraacetic acid and sodium salts thereof, and an inorganic acid, and method of making same |
NL254755A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1959-08-13 |
-
0
- NL NL280590D patent/NL280590A/xx unknown
- BE BE619857D patent/BE619857A/xx unknown
-
1961
- 1961-07-22 DE DEF34511A patent/DE1175431B/de active Pending
- 1961-07-22 DE DEF34510A patent/DE1162557B/de active Pending
- 1961-10-10 DE DEF35104A patent/DE1179365B/de active Pending
- 1961-10-10 DE DEF35105A patent/DE1179366B/de active Pending
-
1962
- 1962-06-12 CH CH704562A patent/CH469035A/de unknown
- 1962-06-22 US US204626A patent/US3314914A/en not_active Expired - Lifetime
- 1962-06-29 FI FI621254A patent/FI42475C/fi active
- 1962-07-04 GB GB25679/62A patent/GB960520A/en not_active Expired
- 1962-07-06 SE SE7615/62A patent/SE303875B/xx unknown
- 1962-07-06 DK DK303662AA patent/DK106247C/da active
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2821519A (en) * | 1955-12-30 | 1958-01-28 | Gen Aniline & Film Corp | Stabilization of polymeric n-vinyl pyrrolidones with hydrazino compounds |
Also Published As
Publication number | Publication date |
---|---|
SE303875B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1968-09-09 |
DE1162557B (de) | 1964-02-06 |
DE1179366B (de) | 1964-10-08 |
FI42475B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1970-04-30 |
FI42475C (fi) | 1970-08-10 |
NL280590A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | |
CH469035A (de) | 1969-02-28 |
DE1179365B (de) | 1964-10-08 |
BE619857A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | |
US3314914A (en) | 1967-04-18 |
GB960520A (en) | 1964-06-10 |
DK106247C (da) | 1967-01-09 |
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