GB1049100A - Plasticized acrylic ester resins - Google Patents
Plasticized acrylic ester resinsInfo
- Publication number
- GB1049100A GB1049100A GB3275563A GB3275563A GB1049100A GB 1049100 A GB1049100 A GB 1049100A GB 3275563 A GB3275563 A GB 3275563A GB 3275563 A GB3275563 A GB 3275563A GB 1049100 A GB1049100 A GB 1049100A
- Authority
- GB
- United Kingdom
- Prior art keywords
- esters
- acid
- acrylic
- plasticized
- ester
- 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
- 229920005989 resin Polymers 0.000 title abstract 16
- 239000011347 resin Substances 0.000 title abstract 16
- -1 acrylic ester Chemical class 0.000 title abstract 11
- 150000002148 esters Chemical class 0.000 abstract 14
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 13
- 239000000194 fatty acid Substances 0.000 abstract 13
- 229930195729 fatty acid Natural products 0.000 abstract 13
- 150000004665 fatty acids Chemical class 0.000 abstract 12
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 8
- 239000006185 dispersion Substances 0.000 abstract 7
- 239000004593 Epoxy Substances 0.000 abstract 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 6
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 abstract 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 abstract 6
- 238000010438 heat treatment Methods 0.000 abstract 6
- 239000000944 linseed oil Substances 0.000 abstract 6
- 235000021388 linseed oil Nutrition 0.000 abstract 6
- 239000003784 tall oil Substances 0.000 abstract 6
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract 5
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 abstract 5
- 239000004014 plasticizer Substances 0.000 abstract 5
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 4
- 229920003180 amino resin Polymers 0.000 abstract 4
- 125000004432 carbon atom Chemical group C* 0.000 abstract 4
- 239000003549 soybean oil Substances 0.000 abstract 4
- 235000012424 soybean oil Nutrition 0.000 abstract 4
- 239000008096 xylene Substances 0.000 abstract 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 abstract 3
- 229910000906 Bronze Inorganic materials 0.000 abstract 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 3
- 239000004606 Fillers/Extenders Substances 0.000 abstract 3
- 239000005909 Kieselgur Substances 0.000 abstract 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 3
- 239000002253 acid Substances 0.000 abstract 3
- 125000002015 acyclic group Chemical group 0.000 abstract 3
- 150000001299 aldehydes Chemical class 0.000 abstract 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 3
- 150000001408 amides Chemical group 0.000 abstract 3
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 abstract 3
- 239000010974 bronze Substances 0.000 abstract 3
- 239000006229 carbon black Substances 0.000 abstract 3
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 3
- 125000004965 chloroalkyl group Chemical group 0.000 abstract 3
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 abstract 3
- 238000000576 coating method Methods 0.000 abstract 3
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 abstract 3
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 3
- 238000004821 distillation Methods 0.000 abstract 3
- 239000003995 emulsifying agent Substances 0.000 abstract 3
- 125000001033 ether group Chemical group 0.000 abstract 3
- 239000000945 filler Substances 0.000 abstract 3
- 235000021384 green leafy vegetables Nutrition 0.000 abstract 3
- 150000004679 hydroxides Chemical class 0.000 abstract 3
- 229910052742 iron Inorganic materials 0.000 abstract 3
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 abstract 3
- 229910044991 metal oxide Inorganic materials 0.000 abstract 3
- 150000004706 metal oxides Chemical class 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 abstract 3
- 239000000049 pigment Substances 0.000 abstract 3
- 229920000642 polymer Polymers 0.000 abstract 3
- 239000000843 powder Substances 0.000 abstract 3
- 235000005713 safflower oil Nutrition 0.000 abstract 3
- 239000003813 safflower oil Substances 0.000 abstract 3
- 150000004760 silicates Chemical class 0.000 abstract 3
- 238000005507 spraying Methods 0.000 abstract 3
- 150000003467 sulfuric acid derivatives Chemical class 0.000 abstract 3
- 239000000454 talc Substances 0.000 abstract 3
- 229910052623 talc Inorganic materials 0.000 abstract 3
- 150000003568 thioethers Chemical class 0.000 abstract 3
- 239000004408 titanium dioxide Substances 0.000 abstract 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 abstract 2
- NXQMCAOPTPLPRL-UHFFFAOYSA-N 2-(2-benzoyloxyethoxy)ethyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCCOCCOC(=O)C1=CC=CC=C1 NXQMCAOPTPLPRL-UHFFFAOYSA-N 0.000 abstract 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 abstract 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 abstract 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 abstract 2
- 229920000742 Cotton Polymers 0.000 abstract 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 abstract 2
- 239000005642 Oleic acid Substances 0.000 abstract 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 abstract 2
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 abstract 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- 229920000297 Rayon Polymers 0.000 abstract 2
- 235000019485 Safflower oil Nutrition 0.000 abstract 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 abstract 2
- 150000007513 acids Chemical class 0.000 abstract 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000003368 amide group Chemical group 0.000 abstract 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 2
- 239000011248 coating agent Substances 0.000 abstract 2
- 239000008199 coating composition Substances 0.000 abstract 2
- 239000007859 condensation product Substances 0.000 abstract 2
- 229920001577 copolymer Polymers 0.000 abstract 2
- 239000004744 fabric Substances 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 abstract 2
- 229910052751 metal Inorganic materials 0.000 abstract 2
- 239000002184 metal Substances 0.000 abstract 2
- 125000005395 methacrylic acid group Chemical class 0.000 abstract 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 abstract 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 abstract 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- ZQHJVIHCDHJVII-OWOJBTEDSA-N (e)-2-chlorobut-2-enedioic acid Chemical compound OC(=O)\C=C(\Cl)C(O)=O ZQHJVIHCDHJVII-OWOJBTEDSA-N 0.000 abstract 1
- PACBIGNRUWABMA-UHFFFAOYSA-N 2-(2,3-dihydro-1,3-benzothiazol-2-yl)-6-dodecyl-4-methylphenol Chemical compound CCCCCCCCCCCCC1=CC(C)=CC(C2SC3=CC=CC=C3N2)=C1O PACBIGNRUWABMA-UHFFFAOYSA-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
- FTABYKMUGGJOES-UHFFFAOYSA-N 2-[6-(2-carboxybenzoyl)oxyhexoxycarbonyl]benzoic acid Chemical compound OC(=O)C1=CC=CC=C1C(=O)OCCCCCCOC(=O)C1=CC=CC=C1C(O)=O FTABYKMUGGJOES-UHFFFAOYSA-N 0.000 abstract 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 abstract 1
- 239000004808 2-ethylhexylester Substances 0.000 abstract 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical group C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 abstract 1
- QZCLKYGREBVARF-UHFFFAOYSA-N Acetyl tributyl citrate Chemical compound CCCCOC(=O)CC(C(=O)OCCCC)(OC(C)=O)CC(=O)OCCCC QZCLKYGREBVARF-UHFFFAOYSA-N 0.000 abstract 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical group C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 1
- 239000005711 Benzoic acid Substances 0.000 abstract 1
- GOJCZVPJCKEBQV-UHFFFAOYSA-N Butyl phthalyl butylglycolate Chemical compound CCCCOC(=O)COC(=O)C1=CC=CC=C1C(=O)OCCCC GOJCZVPJCKEBQV-UHFFFAOYSA-N 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 1
- 229920004934 Dacron® Polymers 0.000 abstract 1
- 229920000877 Melamine resin Polymers 0.000 abstract 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 abstract 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical group CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 abstract 1
- 239000004677 Nylon Substances 0.000 abstract 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 abstract 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 abstract 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract 1
- 239000001089 [(2R)-oxolan-2-yl]methanol Substances 0.000 abstract 1
- 125000002877 alkyl aryl group Chemical group 0.000 abstract 1
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 1
- 239000010775 animal oil Substances 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 235000010233 benzoic acid Nutrition 0.000 abstract 1
- 235000019445 benzyl alcohol Nutrition 0.000 abstract 1
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 abstract 1
- 229940073608 benzyl chloride Drugs 0.000 abstract 1
- 239000011230 binding agent Substances 0.000 abstract 1
- LBKFHGHXATXEBY-UHFFFAOYSA-N bis(1-methylcyclohexyl) benzene-1,2-dicarboxylate Chemical compound C=1C=CC=C(C(=O)OC2(C)CCCCC2)C=1C(=O)OC1(C)CCCCC1 LBKFHGHXATXEBY-UHFFFAOYSA-N 0.000 abstract 1
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 abstract 1
- 230000001680 brushing effect Effects 0.000 abstract 1
- 239000004202 carbamide Substances 0.000 abstract 1
- 239000000919 ceramic Substances 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 abstract 1
- 229940018557 citraconic acid Drugs 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 abstract 1
- QEFOHLDZJZYQEZ-UHFFFAOYSA-N dibutyl 2-(1,4-dibutoxy-1,4-dioxobutan-2-yl)sulfanylbutanedioate Chemical compound CCCCOC(=O)CC(C(=O)OCCCC)SC(C(=O)OCCCC)CC(=O)OCCCC QEFOHLDZJZYQEZ-UHFFFAOYSA-N 0.000 abstract 1
- 238000007598 dipping method Methods 0.000 abstract 1
- 238000001035 drying Methods 0.000 abstract 1
- 238000007590 electrostatic spraying Methods 0.000 abstract 1
- IGOFAIGWJGFDDZ-UHFFFAOYSA-N ethanesulfonamide;toluene Chemical compound CCS(N)(=O)=O.CC1=CC=CC=C1 IGOFAIGWJGFDDZ-UHFFFAOYSA-N 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- XPNLOZNCOBKRNJ-UHFFFAOYSA-N ethyl prop-2-enoate;methyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C=C.COC(=O)C(C)=C XPNLOZNCOBKRNJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000010685 fatty oil Substances 0.000 abstract 1
- 239000001530 fumaric acid Substances 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 150000002430 hydrocarbons Chemical group 0.000 abstract 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 abstract 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 abstract 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 abstract 1
- 150000004702 methyl esters Chemical class 0.000 abstract 1
- 210000000050 mohair Anatomy 0.000 abstract 1
- 150000002763 monocarboxylic acids Chemical class 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
- 229920001778 nylon Polymers 0.000 abstract 1
- 235000021313 oleic acid Nutrition 0.000 abstract 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 abstract 1
- 150000003014 phosphoric acid esters Chemical class 0.000 abstract 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 abstract 1
- 229920002239 polyacrylonitrile Polymers 0.000 abstract 1
- 239000005020 polyethylene terephthalate Substances 0.000 abstract 1
- 229910000027 potassium carbonate Inorganic materials 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- 239000002964 rayon Substances 0.000 abstract 1
- 239000011342 resin composition Substances 0.000 abstract 1
- 238000007761 roller coating Methods 0.000 abstract 1
- 150000003839 salts Chemical group 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 239000000758 substrate Substances 0.000 abstract 1
- BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 abstract 1
- 239000004753 textile Substances 0.000 abstract 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract 1
- 150000003918 triazines Chemical class 0.000 abstract 1
- 150000003672 ureas Chemical class 0.000 abstract 1
- 239000008158 vegetable oil Substances 0.000 abstract 1
- 235000013311 vegetables Nutrition 0.000 abstract 1
- 229920001567 vinyl ester resin Polymers 0.000 abstract 1
- 229920002554 vinyl polymer Polymers 0.000 abstract 1
- 150000008127 vinyl sulfides Chemical class 0.000 abstract 1
- 239000002023 wood Substances 0.000 abstract 1
- 210000002268 wool Anatomy 0.000 abstract 1
- 239000011787 zinc oxide Substances 0.000 abstract 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/38—Compounds containing oxirane rings with hydrocarbon radicals, substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D303/40—Compounds containing oxirane rings with hydrocarbon radicals, substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals by ester radicals
- C07D303/42—Acyclic compounds having a chain of seven or more carbon atoms, e.g. epoxidised fats
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/10—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/12—Radicals substituted by oxygen atoms
-
- 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
- C08K5/1515—Three-membered rings
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09D133/08—Homopolymers or copolymers of acrylic acid esters
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Textile Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Abstract
Epoxy fatty acid esters are prepared by treating with a 40% solution of peracetic acid in acetic acid the esters obtained by:- (a) Heating benzyl alcohol with the methyl ester of safflower oil or soybean oil fatty acids in xylene containing sodium methoxide and removing the methanol evolved by distillation; (b) Adding the chloride of tall oil, soybean oil or linseed oil fatty acids to phenol in chloroform and pyridine; (c) Heating oleic acid, linseed oil fatty acids or tall oil fatty acids with benzyl chloride and potassium carbonate in xylene; (d) Heating tetrahydrofurfuryl alcohol with tall oil, soybean oil or linseed oil fatty acids in xylene in the presence of zinc dust and removing the water of reaction by distillation; (e) Heating under similar conditions as in (d) above cyclohexanol with tall oil, safflower oil or linseed oil fatty acids; (f) Heating tall oil fatty acids with the monobutyl ether of ethylene glycol or diethylene glycol in xylene in the presence of zinc oxide and removing the water of reaction by distillation.ALSO:Resins comprising or consisting of units of at least one ester of acrylic or methacrylic acid and having a solubility parameter d (as defined in the Specification) from 8:4 to 9.7 are plasticized with one or more epoxy esters of the formula RCOOA where R represents the residue of an epoxidized fatty acid and A represents the residue, after removal of a hydroxyl group, of a phenol or an alcohol which is not acyclic, except that A can represent (a) an ether group of the formula R1(OCH2CH2)nOCH2CH2\t where R1 is a C1-C4 alkyl group and n is 0 or an integer from 1 to 4 or (b) a chloroalkyl group containing one or more chlorine atoms. Apart from the specified groups (a) and (b), A generally represents a hydrocarbon group, such as aryl, alkaryl, aralkyl and cycloalkyl, or derivatives thereof containing, for example, halo or hydroxy substituents; A may also represent a heterocyclic group, e.g. furfuryl and derivatives thereof. The residue R of the epoxy ester may contain from 11 to 22 carbon atoms and is typically derived from vegetable or animal oils; for example, R may be derived from oleic acid or safflower oil, soybean oil, linseed oil or tall oil fatty acids. The ester resin is preferably derived from monomeric material containing at least 50% by weight of one or more alkyl or cycloalkyl esters of acrylic or methacrylic acid in which the alkyl or cycloalkyl group contains up to 18 carbon atoms; the resin may also comprise units of vinyl-pyridines, acrylonitrile, methacrylonitrile, acrylic or methacrylic acid and amides and salts thereof, itaconic or citraconic acid and their derivatives, e.e. esters, maleic anhydride, maleic, chloromaleic or fumaric acid and esters of these acids, vinyl ethers, vinyl esters, e.g. vinyl acetate, vinylidene chloride, vinyl sulphides, styrene and its derivatives and analogues thereof, vinylcarbazole, ethylenically unsaturated urea derivatives, allyl esters of monocarboxylic acids, aminoalkyl esters of acrylic and methacrylic acids, hydroxy alkyl esters or amides of acrylic and methacrylic acids, and acrylyl and methacrylyl dicyandiamides. The plasticized compositions may contain other polymers in addition to the acrylic ester resin and may also contain additional plasticizers, e.g. phthalate and phosphate esters, mixed benzoic acid and fatty oil acid esters of pentaerythritol, poly-(propyleneadipate) dibenzoate, diethylene glycol dibenzoate, tetrabutyl thiodisuccinate, butyl phthalyl butyl glycolate, acetyl tributyl citrate, dibenzyl sebacate, toluene ethyl sulphonamide, the di-2-ethylhexyl ester of hexamethylene diphthalate and di(methylcyclohexyl) phthalate. The plasticized composition may be incorporated in a solvent for coating or impregnating purposes and a pigment may also be included, e.g. titanium dioxide, carbon black, iron blues, phthalocyanine blues and greens, metal oxides, hydroxides, sulphides, sulphates, silicates and chromates, aluminium flake, bronze powders, and also a filler or extender, e.g. talc, barytes, china clay and diatomaceous earth. The plasticized esters may also be used in aqueous dispersion containing conventional emulsifiers (many specified) and, if desired, an aminoplast resin, particularly reaction products of aldehydes, e.g. formaldehyde, with compounds such as urea, thiourea, biuret and derivatives thereof, and triazines including melamine and derivatives thereof.ALSO:Substrates such as wood, metal, ceramics, linoleum, vinyl resin tiles and textile fabrics are coated with solutions or aqueous dispersions of plasticized resin compositions comprising an acrylic ester resin comprising or consisting of units of at least one ester of acrylic or methacrylic acid and having a solubility parameter d (as defined in the Specification) from 8.4 to 9.7 and, as plasticizer therefor, one or more epoxy esters of the formula R C O O A where R represents the residue of an epoxidised fatty acid and generally contains from 11 to 22 carbon atoms, and A represents the residue, after removal of a hydronyl group, of a phenol or an alcohol which is not acyclic, except that A can represent (a) on ether group of the formula R1 (O CH2 CH2)n O CH2 CH2 where R1 is a C1-C4 alkyl group and n is O or an integer from 1 to 4 or (b) a chloroalkyl group containing one or more chlorine atoms. The coating compositions may also include other polymers in addition to the aerylic ester resin, additional plasticizers (many specified), pigments, e.g. titanium dioxide, carbon black, iron blues, phthalocyanine blues and greens, metal oxides, hydroxides, sulphides, sulphates, silicates and chromates, aluminium flake, bronze powders, fillers or extenders, e.g. talc, barytes, china clay and diatomaceous earth, and aminoplast resins, particularly condensation products of various amino or amido compounds with aldehydes, e.g. formaldehyde. The aqueous dispersions may also include an emulsifier. Coating may be effected by air-spraying (with or without heating), steam spraying, electrostatic spraying, spraying a preheated coating composition, dipping, brushing or roller-coating. The coatings may be dried at room or elevated temperature, e.g. from 140 DEG to 300 DEG F. In an Example (No. 3), "Dacron" (Registered Trade Mark) taffeta fabric is coated with an aqueous dispersion of a copolymer of methyl methacrylate, methacrylic acid and N-[b -(a -methacryloxyacetamido) ethyl]-N, N1-ethylene urea (96 : 2 : 2) plasticized with the tetrahydrofurfuryl ester of epoxy linseed oil fatty acids; a solution of the same copolymer-plasticiser combination is used to cast a film on a metal (unspecified) sheet.ALSO:The fibres of a non-woven fibrous mass are bound together by impregnating the fibrous mass of, for example, wool, silk, mohair, fur, cotton, linen, rayon, nylon, or acrylonitrile polymers, with a solution or aqueous dispersion of a plasticized acrylic ester resin and drying the impregnated mass. The acrylic ester resin comprises or consists of units of at least one ester of acrylic or methacrylic acid, has a solubility parameter d (as defined in the Specification) from 8.4 to 9.7, and preferably contains groups which form cross-links or can be cross-linked by reaction with aminoplast resins; such groups include amide and N-methylol groups. The resin is plasticized with one or more epoxy esters of the formula RCOOA where R represents the residue of an epoxidized fatty acid and generally contains from 11 to 22 carbon atoms, and A represents the residue, after removal of a hydroxyl group, of a phenol or an alcohol which is not acyclic, except that A can represent (a) an ether group of the formula R1 (O CH2 CH2)n O CH2 CH2 where R1 is a C1 - C4 alkyl group and n is O or an integer from 1 to 4 or (b) a chloroalkyl group containing one or more chlorine atoms. The binder compositions may also include other polymers in addition to the acrylic ester resin, additional plasticizers (many specified), pigments, e.g. titanium dioxide, carbon black, iron blues, phthalocyanine blues and greens, metal oxides, hydroxides, sulphides, sulphates, silicates and chromates, aluminium flake, bronze powders, fillers or extenders, e.g. talc, barytes, china clay and diatomaceous earth, and aminoplast resins, particularly condensation products of various amino or amido compounds with aldehydes, e.g. formaldehyde. The aqueous dispersions may also include an emulsifier. In an Example (No. 6), a non-woven carded web of 75/25 viscose (3 denier, 1 inch staple)-bleached cotton (middling 15/16 inch) is impregnated with an aqueous dispersion of an ethyl acrylate-methyl methacrylate (45:55) copolymer plasticized with the benzyl ester of epoxyoleic acids.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US22008462A | 1962-08-28 | 1962-08-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1049100A true GB1049100A (en) | 1966-11-23 |
Family
ID=22821984
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3275563A Expired GB1049100A (en) | 1962-08-28 | 1963-08-19 | Plasticized acrylic ester resins |
Country Status (4)
| Country | Link |
|---|---|
| BE (1) | BE636698A (en) |
| ES (1) | ES290609A1 (en) |
| GB (1) | GB1049100A (en) |
| NL (1) | NL296556A (en) |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1991000895A1 (en) * | 1989-07-07 | 1991-01-24 | Basf Lacke + Farben Aktiengesellschaft | Process for making a multi-layer paint and basic paint for making the basic layer of a multi-layer paint |
| WO1998015685A1 (en) * | 1996-10-09 | 1998-04-16 | Hercules Incorporated | Ester lubricants as hydrophobic fiber finishes |
| WO1998028356A1 (en) * | 1996-12-24 | 1998-07-02 | Dlw Aktiengesellschaft | Material containing polyreactions products and method for the production thereof |
| WO2000015708A1 (en) * | 1998-09-11 | 2000-03-23 | Ciba Specialty Chemicals Holding Inc. | Polymer compound with improved gloss properties |
| WO2006014483A3 (en) * | 2004-07-08 | 2006-10-05 | Archer Daniels Midland Co | Epoxidized esters of vegetable oil fatty acids as reactive diluents |
| WO2011090812A2 (en) | 2010-01-22 | 2011-07-28 | Archer Daniels Midland Company | Processes for making high purity renewable source-based plasticizers and products made therefrom |
| EP3002301A1 (en) * | 2014-09-30 | 2016-04-06 | Rohm and Haas Company | Aqueous dispersion of composite particles |
| JP2016530384A (en) * | 2013-09-06 | 2016-09-29 | スリーエム イノベイティブ プロパティズ カンパニー | Acid-modified epoxidized vegetable oil and (meth) acrylic copolymer curable composition or cured composition |
| CN113105806A (en) * | 2021-04-08 | 2021-07-13 | 水利部交通运输部国家能源局南京水利科学研究院 | Preparation and use method of coating material for seawater desalination reaction kettle |
-
0
- BE BE636698D patent/BE636698A/xx unknown
- NL NL296556D patent/NL296556A/xx unknown
-
1963
- 1963-08-06 ES ES290609A patent/ES290609A1/en not_active Expired
- 1963-08-19 GB GB3275563A patent/GB1049100A/en not_active Expired
Cited By (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1991000895A1 (en) * | 1989-07-07 | 1991-01-24 | Basf Lacke + Farben Aktiengesellschaft | Process for making a multi-layer paint and basic paint for making the basic layer of a multi-layer paint |
| WO1998015685A1 (en) * | 1996-10-09 | 1998-04-16 | Hercules Incorporated | Ester lubricants as hydrophobic fiber finishes |
| US5972497A (en) * | 1996-10-09 | 1999-10-26 | Fiberco, Inc. | Ester lubricants as hydrophobic fiber finishes |
| WO1998028356A1 (en) * | 1996-12-24 | 1998-07-02 | Dlw Aktiengesellschaft | Material containing polyreactions products and method for the production thereof |
| US6150436A (en) * | 1996-12-24 | 2000-11-21 | Dlw Aktiengesellschaft | Material containing polyreactions products and method for the production thereof |
| WO2000015708A1 (en) * | 1998-09-11 | 2000-03-23 | Ciba Specialty Chemicals Holding Inc. | Polymer compound with improved gloss properties |
| US6569926B1 (en) | 1998-09-11 | 2003-05-27 | Ciba Specialty Chemicals Corporation | Polymer compound with improved gloss properties |
| GB2431160A (en) * | 2004-07-08 | 2007-04-18 | Archer Daniels Midland Co | Epoxidized esters of vegetable oil fatty acids as reactive diluents |
| WO2006014483A3 (en) * | 2004-07-08 | 2006-10-05 | Archer Daniels Midland Co | Epoxidized esters of vegetable oil fatty acids as reactive diluents |
| WO2011090812A2 (en) | 2010-01-22 | 2011-07-28 | Archer Daniels Midland Company | Processes for making high purity renewable source-based plasticizers and products made therefrom |
| US20120277357A1 (en) * | 2010-01-22 | 2012-11-01 | Archer Daniels Midland Company | Processes for making high purity renewable source-based plasticizers and products made therefrom |
| WO2011090812A3 (en) * | 2010-01-22 | 2013-03-14 | Archer Daniels Midland Company | Processes for making high purity renewable source-based plasticizers and products made therefrom |
| US8703849B2 (en) * | 2010-01-22 | 2014-04-22 | Archer Daniels Midland Company | Processes for making high purity renewable source-based plasticizers and products made therefrom |
| JP2016530384A (en) * | 2013-09-06 | 2016-09-29 | スリーエム イノベイティブ プロパティズ カンパニー | Acid-modified epoxidized vegetable oil and (meth) acrylic copolymer curable composition or cured composition |
| EP3002301A1 (en) * | 2014-09-30 | 2016-04-06 | Rohm and Haas Company | Aqueous dispersion of composite particles |
| US9587135B2 (en) | 2014-09-30 | 2017-03-07 | Dow Global Technologies Llc | Aqueous dispersion of composite particles |
| AU2015227422B2 (en) * | 2014-09-30 | 2019-08-01 | Dow Global Technologies Llc | Aqueous dispersion of composite particles |
| CN113105806A (en) * | 2021-04-08 | 2021-07-13 | 水利部交通运输部国家能源局南京水利科学研究院 | Preparation and use method of coating material for seawater desalination reaction kettle |
Also Published As
| Publication number | Publication date |
|---|---|
| NL296556A (en) | |
| BE636698A (en) | |
| ES290609A1 (en) | 1963-12-16 |
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