GB859506A - Stabilized acrylonitrile polymers - Google Patents
Stabilized acrylonitrile polymersInfo
- Publication number
- GB859506A GB859506A GB14360/57A GB1436057A GB859506A GB 859506 A GB859506 A GB 859506A GB 14360/57 A GB14360/57 A GB 14360/57A GB 1436057 A GB1436057 A GB 1436057A GB 859506 A GB859506 A GB 859506A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- vinyl
- component
- ethylene diamine
- diamine tetra
- 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
- 229920002239 polyacrylonitrile Polymers 0.000 title abstract 3
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 abstract 6
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 abstract 6
- 229960001484 edetic acid Drugs 0.000 abstract 6
- 239000000203 mixture Substances 0.000 abstract 5
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 abstract 4
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 abstract 4
- -1 heterocyclic ring compound Chemical class 0.000 abstract 4
- 150000007522 mineralic acids Chemical class 0.000 abstract 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical group O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 abstract 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 abstract 3
- 239000002253 acid Chemical class 0.000 abstract 3
- 125000004432 carbon atom Chemical group C* 0.000 abstract 3
- 239000003153 chemical reaction reagent Substances 0.000 abstract 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 229920001577 copolymer Polymers 0.000 abstract 3
- HRKQOINLCJTGBK-UHFFFAOYSA-N dihydroxidosulfur Chemical compound OSO HRKQOINLCJTGBK-UHFFFAOYSA-N 0.000 abstract 3
- 229910052751 metal Inorganic materials 0.000 abstract 3
- 239000002184 metal Substances 0.000 abstract 3
- 239000000178 monomer Substances 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical class 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 abstract 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 abstract 2
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 2
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical class CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 abstract 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric Acid Chemical compound [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 abstract 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 abstract 2
- FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 abstract 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 abstract 2
- KJFMBFZCATUALV-UHFFFAOYSA-N phenolphthalein Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2C(=O)O1 KJFMBFZCATUALV-UHFFFAOYSA-N 0.000 abstract 2
- 229920000642 polymer Polymers 0.000 abstract 2
- 229910052708 sodium Inorganic materials 0.000 abstract 2
- 239000011734 sodium Substances 0.000 abstract 2
- 239000001488 sodium phosphate Substances 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 2
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 abstract 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 abstract 2
- AGRIQBHIKABLPJ-UHFFFAOYSA-N 1-Pyrrolidinecarboxaldehyde Chemical compound O=CN1CCCC1 AGRIQBHIKABLPJ-UHFFFAOYSA-N 0.000 abstract 1
- DQIRHMDFDOXWHX-UHFFFAOYSA-N 1-bromo-1-chloroethene Chemical group ClC(Br)=C DQIRHMDFDOXWHX-UHFFFAOYSA-N 0.000 abstract 1
- SHVBLBWXKTWTAK-UHFFFAOYSA-N 1-ethenyl-5-methylimidazole Chemical compound CC1=CN=CN1C=C SHVBLBWXKTWTAK-UHFFFAOYSA-N 0.000 abstract 1
- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 abstract 1
- VOCDJQSAMZARGX-UHFFFAOYSA-N 1-ethenylpyrrolidine-2,5-dione Chemical compound C=CN1C(=O)CCC1=O VOCDJQSAMZARGX-UHFFFAOYSA-N 0.000 abstract 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 abstract 1
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 abstract 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- SZTBMYHIYNGYIA-UHFFFAOYSA-M 2-chloroacrylate Chemical compound [O-]C(=O)C(Cl)=C SZTBMYHIYNGYIA-UHFFFAOYSA-M 0.000 abstract 1
- WHBAYNMEIXUTJV-UHFFFAOYSA-N 2-chloroethyl prop-2-enoate Chemical compound ClCCOC(=O)C=C WHBAYNMEIXUTJV-UHFFFAOYSA-N 0.000 abstract 1
- YBXYCBGDIALKAK-UHFFFAOYSA-N 2-chloroprop-2-enamide Chemical compound NC(=O)C(Cl)=C YBXYCBGDIALKAK-UHFFFAOYSA-N 0.000 abstract 1
- QQBUHYQVKJQAOB-UHFFFAOYSA-N 2-ethenylfuran Chemical compound C=CC1=CC=CO1 QQBUHYQVKJQAOB-UHFFFAOYSA-N 0.000 abstract 1
- IGDLZDCWMRPMGL-UHFFFAOYSA-N 2-ethenylisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(C=C)C(=O)C2=C1 IGDLZDCWMRPMGL-UHFFFAOYSA-N 0.000 abstract 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 abstract 1
- KFDVPJUYSDEJTH-UHFFFAOYSA-N 4-ethenylpyridine Chemical compound C=CC1=CC=NC=C1 KFDVPJUYSDEJTH-UHFFFAOYSA-N 0.000 abstract 1
- VJOWMORERYNYON-UHFFFAOYSA-N 5-ethenyl-2-methylpyridine Chemical compound CC1=CC=C(C=C)C=N1 VJOWMORERYNYON-UHFFFAOYSA-N 0.000 abstract 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 abstract 1
- YQPANSWBFWMJFT-UHFFFAOYSA-M C(CCCCCCCCCCCCCCC)SP(=S)(OCCCCCCCCCCCCCCCC)[O-].[Zn+].C(C)(=O)C1=CC=CC=C1 Chemical compound C(CCCCCCCCCCCCCCC)SP(=S)(OCCCCCCCCCCCCCCCC)[O-].[Zn+].C(C)(=O)C1=CC=CC=C1 YQPANSWBFWMJFT-UHFFFAOYSA-M 0.000 abstract 1
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 abstract 1
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 abstract 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 abstract 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 abstract 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 abstract 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 abstract 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 abstract 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 abstract 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical group [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 150000001299 aldehydes Chemical class 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- JMXMXKRNIYCNRV-UHFFFAOYSA-N bis(hydroxymethyl)phosphanylmethanol Chemical compound OCP(CO)CO JMXMXKRNIYCNRV-UHFFFAOYSA-N 0.000 abstract 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-M chloroacetate Chemical compound [O-]C(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-M 0.000 abstract 1
- 229940089960 chloroacetate Drugs 0.000 abstract 1
- 235000015165 citric acid Nutrition 0.000 abstract 1
- YPTLFOZCUOHVFO-SREVYHEPSA-N diethyl (z)-2-methylbut-2-enedioate Chemical compound CCOC(=O)\C=C(\C)C(=O)OCC YPTLFOZCUOHVFO-SREVYHEPSA-N 0.000 abstract 1
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 abstract 1
- 229940093858 ethyl acetoacetate Drugs 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- BSJZCDKNFVVVBW-UHFFFAOYSA-N hydrobromide hydrofluoride Chemical compound F.Br BSJZCDKNFVVVBW-UHFFFAOYSA-N 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- NXPHCVPFHOVZBC-UHFFFAOYSA-N hydroxylamine;sulfuric acid Chemical compound ON.OS(O)(=O)=O NXPHCVPFHOVZBC-UHFFFAOYSA-N 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- HNEGQIOMVPPMNR-NSCUHMNNSA-N mesaconic acid Chemical compound OC(=O)C(/C)=C/C(O)=O HNEGQIOMVPPMNR-NSCUHMNNSA-N 0.000 abstract 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 abstract 1
- 125000005395 methacrylic acid group Chemical class 0.000 abstract 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 abstract 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 abstract 1
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 abstract 1
- 229910017604 nitric acid Inorganic materials 0.000 abstract 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 abstract 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 abstract 1
- 235000006408 oxalic acid Nutrition 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 abstract 1
- 229910052700 potassium Inorganic materials 0.000 abstract 1
- 239000011591 potassium Chemical group 0.000 abstract 1
- 239000004289 sodium hydrogen sulphite Substances 0.000 abstract 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 abstract 1
- 229910000162 sodium phosphate Inorganic materials 0.000 abstract 1
- 235000011008 sodium phosphates Nutrition 0.000 abstract 1
- 159000000000 sodium salts Chemical class 0.000 abstract 1
- VGTPCRGMBIAPIM-UHFFFAOYSA-M sodium thiocyanate Chemical compound [Na+].[S-]C#N VGTPCRGMBIAPIM-UHFFFAOYSA-M 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 abstract 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 1
- 239000001117 sulphuric acid Substances 0.000 abstract 1
- 235000011149 sulphuric acid Nutrition 0.000 abstract 1
- 239000011975 tartaric acid Substances 0.000 abstract 1
- 235000002906 tartaric acid Nutrition 0.000 abstract 1
- DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 abstract 1
- UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 0.000 abstract 1
- 229910000406 trisodium phosphate Inorganic materials 0.000 abstract 1
- 235000019801 trisodium phosphate Nutrition 0.000 abstract 1
- MLIKYFGFHUYZAL-UHFFFAOYSA-K trisodium;hydron;phosphonato phosphate Chemical compound [Na+].[Na+].[Na+].OP([O-])(=O)OP([O-])([O-])=O MLIKYFGFHUYZAL-UHFFFAOYSA-K 0.000 abstract 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 abstract 1
- 229910052725 zinc Chemical group 0.000 abstract 1
- 239000011701 zinc Chemical group 0.000 abstract 1
- 239000011592 zinc chloride Substances 0.000 abstract 1
- 235000005074 zinc chloride Nutrition 0.000 abstract 1
- PENRVBJTRIYHOA-UHFFFAOYSA-L zinc dithionite Chemical compound [Zn+2].[O-]S(=O)S([O-])=O PENRVBJTRIYHOA-UHFFFAOYSA-L 0.000 abstract 1
- ILSSWSPLQXNOCJ-UHFFFAOYSA-L zinc;hexadecoxy-hexadecylsulfanyl-oxido-sulfanylidene-$l^{5}-phosphane Chemical compound [Zn+2].CCCCCCCCCCCCCCCCOP([O-])(=S)SCCCCCCCCCCCCCCCC.CCCCCCCCCCCCCCCCOP([O-])(=S)SCCCCCCCCCCCCCCCC ILSSWSPLQXNOCJ-UHFFFAOYSA-L 0.000 abstract 1
Classifications
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- 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/5398—Phosphorus bound to sulfur
-
- 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
- C08K13/00—Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
- C08K13/02—Organic and inorganic ingredients
-
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/24—Acids; 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/30—Sulfur-, selenium- or tellurium-containing compounds
-
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/32—Phosphorus-containing compounds
-
- 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
-
- 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
- C08K5/01—Hydrocarbons
-
- 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
- C08K5/07—Aldehydes; Ketones
-
- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/101—Esters; Ether-esters of monocarboxylic acids
-
- 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
- C08K5/13—Phenols; Phenolates
-
- 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
- C08K5/15—Heterocyclic compounds having oxygen in the ring
- C08K5/151—Heterocyclic compounds having oxygen in the ring having one oxygen atom in the ring
- C08K5/1535—Five-membered rings
-
- 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
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- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
- C08K5/3415—Five-membered rings
-
- 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
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
- C08K5/3432—Six-membered rings
- C08K5/3435—Piperidines
-
- 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
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3442—Heterocyclic compounds having nitrogen in the ring having two nitrogen atoms in the ring
- C08K5/3462—Six-membered rings
-
- 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
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/35—Heterocyclic compounds having nitrogen in the ring having also oxygen in the ring
-
- 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
- C08K5/41—Compounds containing sulfur bound to oxygen
-
- 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
- C08K5/41—Compounds containing sulfur bound to oxygen
- C08K5/42—Sulfonic acids; Derivatives 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
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- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/521—Esters of phosphoric acids, e.g. of H3PO4
- C08K5/523—Esters of phosphoric acids, e.g. of H3PO4 with hydroxyaryl compounds
-
- 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/524—Esters of phosphorous acids, e.g. of H3PO3
-
- 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only
- C08K5/5317—Phosphonic compounds, e.g. R—P(:O)(OR')2
-
- 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only
- C08K5/5393—Phosphonous compounds, e.g. R—P(OR')2
-
- 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only
- C08K5/5397—Phosphine oxides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or 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 of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/18—Homopolymers or copolymers of nitriles
- C08L33/20—Homopolymers or copolymers of acrylonitrile
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)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Artificial Filaments (AREA)
- Phenolic Resins Or Amino Resins (AREA)
Applications Claiming Priority (36)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US58667956A | 1956-05-23 | 1956-05-23 | |
| US586676A US2878219A (en) | 1956-05-23 | 1956-05-23 | Acrylonitrile polymer composition stabilized with tricresyl phosphate and an inorganic acid and method of making same |
| US586666A US2878211A (en) | 1956-05-23 | 1956-05-23 | Acrylonitrile polymer composition stabilized with formaldehyde, acetophenone, and inorganic acid and method of making same |
| US586680A US2878222A (en) | 1956-05-23 | 1956-05-23 | Acrylonitrile polymer composition stabilized with metal formaldehyde sulfoxylate, formaldehyde, and acetic acid and method of making same |
| US586675A US2878200A (en) | 1956-05-23 | 1956-05-23 | Stabilized acrylonitrile polymer composition and method of preparing same |
| US586683A US2878224A (en) | 1956-05-23 | 1956-05-23 | Acrylonitrile compositions stabilized with metal formaldehyde sulfoxylate and an inorganic acid and method of making same |
| US586664A US2878209A (en) | 1956-05-23 | 1956-05-23 | Acrylonitrile polymer composition stabilized with formaldehyde, hydroxylamine sulfate, and an inorganic acid, and method of making same |
| US586662A US2878207A (en) | 1956-05-23 | 1956-05-23 | Acrylonitrile polymer composition stabilized with acrolein, a phenol, and an inorganic acid, and method of making same |
| US586670A US2878215A (en) | 1956-05-23 | 1956-05-23 | Stabilized acrylonitrile polymer composition stabilized with dicyclopentadiene and an inorganic acid and methof of making same |
| US586658A US2878203A (en) | 1956-05-23 | 1956-05-23 | Acrylonitrile polymer composition stabilized with metal formaldehyde sulfoxylate, a six membered n-formyl heterocyclic compound, and an inorganic acid, and method of making same |
| US586660A US2878205A (en) | 1956-05-23 | 1956-05-23 | Acrylonitrile polymer composition stabilized with formaldehyde, a substituted phenol, and acetic anhydride, and method of making same |
| US586682A US2849413A (en) | 1956-05-23 | 1956-05-23 | Acrylonitrile compositions stabilized with metal formaldehyde sulfoxylates, zinc dicetyl dithiophosphate, and inorganic acids, and method of making |
| US586684A US2878225A (en) | 1956-05-23 | 1956-05-23 | Acrylonitrile polymer composition stabilized with metal formaldehyde sulfoxylate, analkali phosphate, and an inorganic acid and method of making same |
| US586671A US2878216A (en) | 1956-05-23 | 1956-05-23 | Acrylonitrile polymer composition stabilized with phenolphthalein and an inorganic acid and method of making same |
| US586659A US2878204A (en) | 1956-05-23 | 1956-05-23 | Acrylonitrile polymer composition stabilized with metal formaldehyde sulfoxylate, ethylenediamine tetra-acetic acid and sodium salts thereof, and an inorganic acid, and method of making same |
| US586668A US2878213A (en) | 1956-05-23 | 1956-05-23 | Acrylonitrile polymer composition stabilized with formaldehyde, zinc dicetyldithiophosphate, and an inorganic acid and method of making same |
| US586677A US2878220A (en) | 1956-05-23 | 1956-05-23 | Acrylonitrile polymer composition comprising a six membered heterocyclic n-substituted aldehyde and an inorganic acid and process of making same |
| US586669A US2878214A (en) | 1956-05-23 | 1956-05-23 | Acrylonitrile polymer composition stabilized with formaldehyde, an alkali sulfite and an inorganic acid and method of making same |
| US586681A US2878223A (en) | 1956-05-23 | 1956-05-23 | Acrylonitrile polymer composition stabilized with metal formaldehyde sulfoxylate, formaldehyde, and acetic anhydride and method of making same |
| US586672A US2878217A (en) | 1956-05-23 | 1956-05-23 | Acrylonitrile polymer composition stabilized with an inorganic acid and cumene and method of making same |
| US586685A US2946760A (en) | 1956-05-23 | 1956-05-23 | Stabilized acrylonitrile polymer composition and method of making same |
| US586663A US2878208A (en) | 1956-05-23 | 1956-05-23 | Acrylonitrile polymer composition stabilized with formaldehyde, ethylenediamine tetraacetic acid and sodium salts thereof, and an inorganic acid, and method of making same |
| US586674A US2878218A (en) | 1956-05-23 | 1956-05-23 | Acrylonitrile polymer composition stabilized with formaldehyde, a phosphate, and an inorganic acid and method of making same |
| US586678A US2878221A (en) | 1956-05-23 | 1956-05-23 | Acrylonitrile polymer composition stabilized with metal formaldehyde sulfoxylate and formaldehyde and method of making same |
| US586661A US2878206A (en) | 1956-05-23 | 1956-05-23 | Acrylonitrile polymer composition stabilized with metal formaldehyde sulfoxylate, a weak acid, and an inorganic acid and method of making same |
| US586667A US2878212A (en) | 1956-05-23 | 1956-05-23 | Acrylonitrile polymer composition stabilized with formaldehyde, a phenol, and an inorganic acid and method of making same |
| US586665A US2878210A (en) | 1956-05-23 | 1956-05-23 | Acrylonitrile polymer composition stabilized with formaldehyde, ethylacetoacetate, and an inorganic acid, and method of making same |
| US628533A US2850472A (en) | 1956-05-23 | 1956-12-17 | Color stabilized acrylonitrile polymers and method of making the same |
| US628488A US2878226A (en) | 1956-12-17 | 1956-12-17 | Acrylonitrile polymer composition stabilized with metal formaldehyde sulfoxylate and methylol sulfonic acid and method of making same |
| US628532A US2878230A (en) | 1956-05-23 | 1956-12-17 | Acrylonitrile polymer composition stabilized with metal formaldehyde sulfoxylate and phenol disulfonic acid and method of making same |
| US628530A US2878228A (en) | 1956-12-17 | 1956-12-17 | Acrylonitrile polymer composition stabilized with formaldehyde, tris (hydroxymethyl)phosphonium oxide, and hydrochloric acid, and method of making same |
| US628490A US2878202A (en) | 1956-12-17 | 1956-12-17 | Acrylonitrile polymer composition stabilized with the zinc reduction product of methylol sulfonic acid and method of making same |
| US628531A US2878229A (en) | 1956-05-23 | 1956-12-17 | Acrylonitrile polymer composition stabilized with metal formaldehyde sulfoxylate andan organic phosphite, and method of making same |
| US628489A US2878227A (en) | 1956-12-17 | 1956-12-17 | Acrylonitrile polymer compositions stabilized with paraformaldehyde and trialkyl subsituted phosphites, and method of making same |
| US633374A US2878231A (en) | 1956-05-23 | 1957-01-09 | Acrylonitrile polymer composition stabilized with metal formaldehyde sulfoxylate, phosphorus pentroxide, and sulfuric acid and method of making same |
| US833369A US2982753A (en) | 1956-05-23 | 1959-08-13 | Composition containing acrylonitrile polymers and color inhibiting agents therefor and method of making |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB859506A true GB859506A (en) | 1961-01-25 |
Family
ID=27586950
Family Applications (5)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB19747/59A Expired GB859508A (en) | 1956-05-23 | 1957-05-06 | Stabilized acrylonitrile polymers |
| GB19746/59A Expired GB859507A (en) | 1956-05-23 | 1957-05-06 | Stabilized acrylonitrile polymers |
| GB19748/59A Expired GB859509A (en) | 1956-05-23 | 1957-05-06 | Stabilized acrylonitrile polymers |
| GB14360/57A Expired GB859506A (en) | 1956-05-23 | 1957-05-06 | Stabilized acrylonitrile polymers |
| GB19749/59A Expired GB859510A (en) | 1956-05-23 | 1957-05-06 | Stabilized acrylonitrile polymers |
Family Applications Before (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB19747/59A Expired GB859508A (en) | 1956-05-23 | 1957-05-06 | Stabilized acrylonitrile polymers |
| GB19746/59A Expired GB859507A (en) | 1956-05-23 | 1957-05-06 | Stabilized acrylonitrile polymers |
| GB19748/59A Expired GB859509A (en) | 1956-05-23 | 1957-05-06 | Stabilized acrylonitrile polymers |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB19749/59A Expired GB859510A (en) | 1956-05-23 | 1957-05-06 | Stabilized acrylonitrile polymers |
Country Status (5)
| Country | Link |
|---|---|
| US (6) | US2878210A (enExample) |
| BE (1) | BE557745A (enExample) |
| FR (1) | FR1179200A (enExample) |
| GB (5) | GB859508A (enExample) |
| NL (20) | NL106195C (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001017950A1 (en) * | 1999-09-09 | 2001-03-15 | E.I. Du Pont De Nemours And Company | Treatment of nitriles with glycolic acid |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3172869A (en) * | 1965-03-09 | Acryloniteils resins plasticized with a cyangethylated amide | ||
| US3055861A (en) * | 1958-02-19 | 1962-09-25 | Union Carbide Corp | Stabilized acrylonitrile vinyl or vinylidene copolymer solutions |
| US2951055A (en) * | 1959-01-30 | 1960-08-30 | American Cyanamid Co | Stabilization of acrylonitrile copolymers |
| NL133429C (enExample) * | 1959-08-13 | |||
| NL283235A (enExample) * | 1960-10-07 | |||
| BE620089A (enExample) * | 1961-07-11 | |||
| NL123741C (enExample) * | 1962-09-05 | |||
| DE1268382B (de) * | 1962-11-02 | 1968-05-16 | Bayer Ag | Vergilbungsstabilisator fuer Loesungen von Acrylnitrilpolymerisaten in organischen Loesungsmitteln |
| DE1268383B (de) * | 1962-11-02 | 1968-05-16 | Bayer Ag | Vergilbungsstabilisator fuer Loesungen von Acrylnitrilpolymerisaten in organischen Loesungsmitteln |
| US3322716A (en) * | 1963-08-19 | 1967-05-30 | American Cyanamid Co | Flame retardant compositions consisting essentially of a thermoplastic material and a phosphinic acid |
| NL124223C (enExample) * | 1964-05-19 | |||
| DE1544882C3 (de) * | 1964-08-24 | 1975-03-13 | Bayer Ag, 5090 Leverkusen | Stabilisierte Spinnlösungen von Copolymerisaten des Acrylnitril mit Vinylidenchlorid |
| US3917553A (en) * | 1971-04-22 | 1975-11-04 | Celanese Corp | Stabilized polyacrylonitrile compositions with sulfur containing stabilizer and method of forming same |
| US4055532A (en) * | 1973-06-04 | 1977-10-25 | Celanese Corporation | Stabilized acetonitrile solvent containing polyacrylonitrile compositions and method of forming same |
| US4077929A (en) * | 1975-03-06 | 1978-03-07 | E. I. Du Pont De Nemours And Company | Process for producing flame-resistant filaments |
| US4211722A (en) * | 1979-03-07 | 1980-07-08 | E. I. Du Pont De Nemours & Co. | Formaldehyde stabilization of acrylonitrile against color |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2502030A (en) * | 1945-07-13 | 1950-03-28 | Du Pont | Solutions of acrylonitrile polymers containing a color-free acidic compound |
| NL80808C (enExample) * | 1949-10-27 | |||
| US2642408A (en) * | 1950-04-15 | 1953-06-16 | Eastman Kodak Co | Stabilized solutions of acrylonitrile polymers and stabilized solvent |
-
0
- NL NL273608D patent/NL273608A/xx unknown
- NL NL273600D patent/NL273600A/xx unknown
-
1956
- 1956-05-23 US US586665A patent/US2878210A/en not_active Expired - Lifetime
- 1956-12-17 US US628533A patent/US2850472A/en not_active Expired - Lifetime
- 1956-12-17 US US628531A patent/US2878229A/en not_active Expired - Lifetime
- 1956-12-17 US US628532A patent/US2878230A/en not_active Expired - Lifetime
-
1957
- 1957-01-09 US US633374A patent/US2878231A/en not_active Expired - Lifetime
- 1957-05-06 GB GB19747/59A patent/GB859508A/en not_active Expired
- 1957-05-06 GB GB19746/59A patent/GB859507A/en not_active Expired
- 1957-05-06 GB GB19748/59A patent/GB859509A/en not_active Expired
- 1957-05-06 GB GB14360/57A patent/GB859506A/en not_active Expired
- 1957-05-06 GB GB19749/59A patent/GB859510A/en not_active Expired
- 1957-05-22 FR FR1179200D patent/FR1179200A/fr not_active Expired
- 1957-05-22 NL NL217497A patent/NL106195C/xx active
- 1957-05-23 BE BE557745D patent/BE557745A/xx unknown
-
1959
- 1959-08-13 US US833369A patent/US2982753A/en not_active Expired - Lifetime
-
1962
- 1962-01-16 NL NL273602A patent/NL109482C/xx active
- 1962-01-16 NL NL273605A patent/NL110921C/xx active
- 1962-01-16 NL NL273606A patent/NL108760C/xx active
- 1962-01-16 NL NL273603A patent/NL110920C/xx active
- 1962-01-16 NL NL273601A patent/NL108759C/xx active
- 1962-01-16 NL NL273604A patent/NL108986C/xx active
- 1962-01-16 NL NL273607A patent/NL109237C/xx active
-
1964
- 1964-02-20 NL NL6401579A patent/NL6401579A/xx unknown
- 1964-02-20 NL NL6401582A patent/NL6401582A/xx unknown
- 1964-02-20 NL NL6401583A patent/NL6401583A/xx unknown
- 1964-02-20 NL NL6401581A patent/NL6401581A/xx unknown
- 1964-02-20 NL NL6401580A patent/NL6401580A/xx unknown
- 1964-02-21 NL NL6401650A patent/NL6401650A/xx unknown
- 1964-02-21 NL NL6401649A patent/NL6401649A/xx unknown
- 1964-04-03 NL NL6403581A patent/NL6403581A/xx unknown
- 1964-04-13 NL NL6403972A patent/NL6403972A/xx unknown
- 1964-04-13 NL NL6403973A patent/NL6403973A/xx unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001017950A1 (en) * | 1999-09-09 | 2001-03-15 | E.I. Du Pont De Nemours And Company | Treatment of nitriles with glycolic acid |
Also Published As
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