CA2763765C - Slip and antiblocking agent - Google Patents
Slip and antiblocking agent Download PDFInfo
- Publication number
- CA2763765C CA2763765C CA2763765A CA2763765A CA2763765C CA 2763765 C CA2763765 C CA 2763765C CA 2763765 A CA2763765 A CA 2763765A CA 2763765 A CA2763765 A CA 2763765A CA 2763765 C CA2763765 C CA 2763765C
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- fatty acid
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- Prior art date
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- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 83
- 239000000194 fatty acid Substances 0.000 claims abstract description 83
- 229930195729 fatty acid Natural products 0.000 claims abstract description 83
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 81
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 45
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 38
- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract 10
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 53
- 229920000642 polymer Polymers 0.000 claims description 51
- 239000000203 mixture Substances 0.000 claims description 42
- 238000000034 method Methods 0.000 claims description 29
- 239000004202 carbamide Substances 0.000 claims description 27
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 20
- 230000008569 process Effects 0.000 claims description 20
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 19
- 229920000098 polyolefin Polymers 0.000 claims description 16
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 15
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 11
- 229910021529 ammonia Inorganic materials 0.000 claims description 10
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 9
- 239000004793 Polystyrene Substances 0.000 claims description 9
- 229910052740 iodine Inorganic materials 0.000 claims description 9
- 239000011630 iodine Substances 0.000 claims description 9
- 229920002223 polystyrene Polymers 0.000 claims description 9
- 239000003054 catalyst Substances 0.000 claims description 8
- 238000007670 refining Methods 0.000 claims description 8
- 238000002360 preparation method Methods 0.000 claims description 6
- 239000002356 single layer Substances 0.000 claims description 4
- 230000002862 amidating effect Effects 0.000 claims description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
- 239000011369 resultant mixture Substances 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 abstract description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 48
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 40
- 239000010408 film Substances 0.000 description 25
- 239000002253 acid Substances 0.000 description 24
- 150000001408 amides Chemical class 0.000 description 24
- 239000000377 silicon dioxide Substances 0.000 description 24
- 239000012748 slip agent Substances 0.000 description 22
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
- 230000000052 comparative effect Effects 0.000 description 21
- 230000003068 static effect Effects 0.000 description 16
- KZVIUXKOLXVBPC-UHFFFAOYSA-N 16-methylheptadecanamide Chemical compound CC(C)CCCCCCCCCCCCCCC(N)=O KZVIUXKOLXVBPC-UHFFFAOYSA-N 0.000 description 15
- -1 aliphatic saturated Chemical class 0.000 description 14
- UAUDZVJPLUQNMU-UHFFFAOYSA-N Erucasaeureamid Natural products CCCCCCCCC=CCCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-UHFFFAOYSA-N 0.000 description 12
- UAUDZVJPLUQNMU-KTKRTIGZSA-N erucamide Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-KTKRTIGZSA-N 0.000 description 12
- 150000002430 hydrocarbons Chemical group 0.000 description 12
- 239000000243 solution Substances 0.000 description 10
- 125000000217 alkyl group Chemical group 0.000 description 9
- 239000002981 blocking agent Substances 0.000 description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- 238000004821 distillation Methods 0.000 description 8
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 8
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 7
- 239000000654 additive Substances 0.000 description 7
- 239000012267 brine Substances 0.000 description 7
- 229920001577 copolymer Polymers 0.000 description 7
- 239000000706 filtrate Substances 0.000 description 7
- 239000010410 layer Substances 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 6
- 239000000178 monomer Substances 0.000 description 6
- 230000001590 oxidative effect Effects 0.000 description 6
- 239000004594 Masterbatch (MB) Substances 0.000 description 5
- 239000004698 Polyethylene Substances 0.000 description 5
- 238000002835 absorbance Methods 0.000 description 5
- 230000000996 additive effect Effects 0.000 description 5
- 239000013078 crystal Substances 0.000 description 5
- 229920001684 low density polyethylene Polymers 0.000 description 5
- 239000004702 low-density polyethylene Substances 0.000 description 5
- 229920000573 polyethylene Polymers 0.000 description 5
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 5
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 5
- HJVKLVGLKNGYGQ-UHFFFAOYSA-N 20-methylhenicosanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCCCCCC(O)=O HJVKLVGLKNGYGQ-UHFFFAOYSA-N 0.000 description 4
- ORAWFNKFUWGRJG-UHFFFAOYSA-N Docosanamide Chemical compound CCCCCCCCCCCCCCCCCCCCCC(N)=O ORAWFNKFUWGRJG-UHFFFAOYSA-N 0.000 description 4
- 239000005977 Ethylene Substances 0.000 description 4
- 239000004743 Polypropylene Substances 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 229920001155 polypropylene Polymers 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 230000009467 reduction Effects 0.000 description 4
- 229940037312 stearamide Drugs 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 230000000903 blocking effect Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 229920001519 homopolymer Polymers 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- FHSJASSJVNBPOX-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O.CCCCCCCCCCCCCCCCCC(N)=O FHSJASSJVNBPOX-UHFFFAOYSA-N 0.000 description 3
- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 description 3
- FATBGEAMYMYZAF-UHFFFAOYSA-N oleicacidamide-heptaglycolether Natural products CCCCCCCCC=CCCCCCCCC(N)=O FATBGEAMYMYZAF-UHFFFAOYSA-N 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 238000001953 recrystallisation Methods 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 150000004671 saturated fatty acids Chemical class 0.000 description 3
- 239000010409 thin film Substances 0.000 description 3
- CFQZKFWQLAHGSL-FNTYJUCDSA-N (3e,5e,7e,9e,11e,13e,15e,17e)-18-[(3e,5e,7e,9e,11e,13e,15e,17e)-18-[(3e,5e,7e,9e,11e,13e,15e)-octadeca-3,5,7,9,11,13,15,17-octaenoyl]oxyoctadeca-3,5,7,9,11,13,15,17-octaenoyl]oxyoctadeca-3,5,7,9,11,13,15,17-octaenoic acid Chemical compound OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C CFQZKFWQLAHGSL-FNTYJUCDSA-N 0.000 description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- WNWHHMBRJJOGFJ-UHFFFAOYSA-N 16-methylheptadecan-1-ol Chemical compound CC(C)CCCCCCCCCCCCCCCO WNWHHMBRJJOGFJ-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 2
- 230000009435 amidation Effects 0.000 description 2
- 238000007112 amidation reaction Methods 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 239000000539 dimer Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 150000002193 fatty amides Chemical class 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- HSEMFIZWXHQJAE-UHFFFAOYSA-N hexadecanamide Chemical compound CCCCCCCCCCCCCCCC(N)=O HSEMFIZWXHQJAE-UHFFFAOYSA-N 0.000 description 2
- 229920005669 high impact polystyrene Polymers 0.000 description 2
- 239000004797 high-impact polystyrene Substances 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 150000002763 monocarboxylic acids Chemical class 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
- 229920005606 polypropylene copolymer Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 235000003441 saturated fatty acids Nutrition 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- OXDXXMDEEFOVHR-CLFAGFIQSA-N (z)-n-[2-[[(z)-octadec-9-enoyl]amino]ethyl]octadec-9-enamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)NCCNC(=O)CCCCCCC\C=C/CCCCCCCC OXDXXMDEEFOVHR-CLFAGFIQSA-N 0.000 description 1
- FUSNPOOETKRESL-ZPHPHTNESA-N (z)-n-octadecyldocos-13-enamide Chemical compound CCCCCCCCCCCCCCCCCCNC(=O)CCCCCCCCCCC\C=C/CCCCCCCC FUSNPOOETKRESL-ZPHPHTNESA-N 0.000 description 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound 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 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000010101 extrusion blow moulding Methods 0.000 description 1
- 229910001657 ferrierite group Inorganic materials 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- 238000001640 fractional crystallisation Methods 0.000 description 1
- 239000002828 fuel tank Substances 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 238000007037 hydroformylation reaction Methods 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- RKISUIUJZGSLEV-UHFFFAOYSA-N n-[2-(octadecanoylamino)ethyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCNC(=O)CCCCCCCCCCCCCCCCC RKISUIUJZGSLEV-UHFFFAOYSA-N 0.000 description 1
- DJWFNQUDPJTSAD-UHFFFAOYSA-N n-octadecyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCCNC(=O)CCCCCCCCCCCCCCCCC DJWFNQUDPJTSAD-UHFFFAOYSA-N 0.000 description 1
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000002889 oleic acids Chemical class 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000012766 organic filler Substances 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 229920005629 polypropylene homopolymer Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 229920001384 propylene homopolymer Polymers 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000006462 rearrangement reaction Methods 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L sodium sulphate Substances [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 238000012430 stability testing Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000011145 styrene acrylonitrile resin Substances 0.000 description 1
- 238000003856 thermoforming Methods 0.000 description 1
- 229920002397 thermoplastic olefin Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/26—Carboxylic acids; Salts thereof
- C10M129/28—Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M129/38—Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 8 or more carbon atoms
- C10M129/40—Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 8 or more carbon atoms monocarboxylic
-
- 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
- C08K5/20—Carboxylic acid amides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/02—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
- C07C233/04—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with carbon atoms of carboxamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C233/05—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with carbon atoms of carboxamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to acyclic carbon 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
- C08K2201/00—Specific properties of additives
- C08K2201/014—Additives containing two or more different additives of the same subgroup in C08K
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0910781.4 | 2009-06-23 | ||
| GBGB0910781.4A GB0910781D0 (en) | 2009-06-23 | 2009-06-23 | Slip and antiblocking agent |
| PCT/GB2010/001197 WO2010149952A2 (en) | 2009-06-23 | 2010-06-18 | Slip and antiblocking agent |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2763765A1 CA2763765A1 (en) | 2010-12-29 |
| CA2763765C true CA2763765C (en) | 2015-11-03 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2763765A Active CA2763765C (en) | 2009-06-23 | 2010-06-18 | Slip and antiblocking agent |
Country Status (8)
| Country | Link |
|---|---|
| US (2) | US8865809B2 (enExample) |
| EP (1) | EP2445865B1 (enExample) |
| JP (2) | JP2012530773A (enExample) |
| CN (1) | CN102596895B (enExample) |
| CA (1) | CA2763765C (enExample) |
| ES (1) | ES2689426T3 (enExample) |
| GB (1) | GB0910781D0 (enExample) |
| WO (1) | WO2010149952A2 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108578044A (zh) * | 2011-03-17 | 2018-09-28 | 康沃特克科技公司 | 高阻隔性弹性体粪便导管或造口袋 |
| GB201219224D0 (en) | 2012-10-25 | 2012-12-12 | Croda Int Plc | Process |
| US10557025B2 (en) * | 2015-05-07 | 2020-02-11 | Fine Organics Industries Pvt Ltd. | Polypropylene cap or film composition |
| JP2017025315A (ja) * | 2015-07-24 | 2017-02-02 | Ｍｃｐｐイノベーション合同会社 | 熱可塑性エラストマー組成物、成形体及び自動車用部品 |
| WO2017097364A1 (de) * | 2015-12-10 | 2017-06-15 | Actega Ds Gmbh | Gleitmittelsystem |
| WO2017157410A1 (de) * | 2016-03-14 | 2017-09-21 | Constantia Hueck Folien Gmbh & Co. Kg | Mehrschichtige siegelfolie und folienlaminat mit mehrschichtiger siegelfolie |
| KR102684839B1 (ko) * | 2017-01-11 | 2024-07-17 | 보스틱, 인크. | 압출 가공이 가능한 김서림방지 코폴리에스테르 열 밀봉 수지 |
| ES2938651T3 (es) | 2017-07-26 | 2023-04-13 | Ineos Styrolution Group Gmbh | Composición de copolímeros de estireno resistente a los arañazos que contiene cera de amida |
| TWI862528B (zh) * | 2018-12-14 | 2024-11-21 | 美商陶氏全球科技有限責任公司 | 含有助滑劑之多層膜及層合物 |
| WO2021043785A1 (en) | 2019-09-03 | 2021-03-11 | Sabic Global Technologies B.V. | A pipe containing carboxylic acid amide for the transport of water containing chlorinated disinfectant |
| US12522676B2 (en) | 2020-07-15 | 2026-01-13 | Dow Global Technologies Llc | Polyethylene-based compositions and films made from same |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2013108A (en) * | 1932-07-06 | 1935-09-03 | Ig Farbenindustrie Ag | Production of carboxylic amides |
| US2770609A (en) | 1953-08-26 | 1956-11-13 | Du Pont | Polyethylene-oleamide composition |
| JPS4813935B1 (enExample) * | 1967-10-05 | 1973-05-01 | ||
| JPS4813935Y1 (enExample) | 1969-09-22 | 1973-04-17 | ||
| US4277410A (en) * | 1980-05-02 | 1981-07-07 | Emery Industries, Inc. | Process for the production of carboxylic amides using alkyltin catalysts |
| US4839234A (en) | 1986-05-13 | 1989-06-13 | Sumitomo Chemical Company, Limited | Polypropylene film |
| NL8902182A (nl) | 1989-08-29 | 1991-03-18 | Unilever Nv | Werkwijze voor het opwerken van vetzuren en hieruit bereide esters met een laag stolpunt. |
| JPH03197540A (ja) * | 1989-12-27 | 1991-08-28 | Du Pont Mitsui Polychem Co Ltd | 延伸フィルム押出コート用エチレン共重合体組成物および押出コート方法 |
| GB9018142D0 (en) | 1990-08-17 | 1990-10-03 | Unilever Plc | Slip and antiblock agent for polyolefin films |
| DE4123084A1 (de) * | 1991-07-12 | 1993-01-14 | Hoechst Ag | Verfahren zur abtrennung aliphatischer geradkettiger verbindungen mit endstaendigen funktionellen gruppen |
| JP3303947B2 (ja) * | 1994-05-18 | 2002-07-22 | 花王株式会社 | 分岐脂肪酸及び分岐脂肪酸エステルの製造法 |
| JP2946176B2 (ja) * | 1994-06-27 | 1999-09-06 | 株式会社ノダ | モール |
| EP0774451B2 (en) | 1995-11-16 | 2002-09-11 | Unichema Chemie B.V. | Fatty acid isomerisation |
| JP3850491B2 (ja) * | 1996-08-13 | 2006-11-29 | 旭化成ケミカルズ株式会社 | 樹脂フィルム及びその製造方法 |
| US6177387B1 (en) * | 1996-08-30 | 2001-01-23 | Exxon Chemical Patents Inc | Reduced odor and high stability aircraft turbine oil base stock |
| GB9700671D0 (en) | 1997-01-14 | 1997-03-05 | Croda Int Plc | Woolgrease |
| ES2141696T1 (es) | 1997-04-16 | 2000-04-01 | Dow Chemical Co | Composiciones que contienen agentes de deslizamiento y de antibloqueo. |
| JPH1110811A (ja) * | 1997-06-25 | 1999-01-19 | Kureha Plast Kk | 多層ストレッチフィルム |
| IL121268A0 (en) * | 1997-07-09 | 1998-01-04 | Dpharm Ltd | Branched chain fatty acids their derivatives and use in the treatment of central nervous system disorders |
| US6518311B2 (en) * | 1997-07-09 | 2003-02-11 | D-Pharm Ltd. | Use of branched-chain fatty acids and derivatives thereof for the treatment of pain |
| US6497965B1 (en) | 1997-10-09 | 2002-12-24 | Applied Extrusion Technologies, Inc. | Slip agents and polypropylene films prepared therefrom |
| GB2378705B (en) * | 1998-08-26 | 2003-03-26 | Pvaxx Technologies Ltd | PVA-Containing compositions |
| JP2003523975A (ja) * | 2000-02-07 | 2003-08-12 | ヤン、ツェンファ | 特異構造を持つ抗癌化合物群及びその生産方法 |
| EP1136524A1 (fr) * | 2000-03-22 | 2001-09-26 | SOLVAY POLYOLEFINS EUROPE - BELGIUM (Société Anonyme) | Composition à base de polyéthylène et procédé de fabrication d'objets façonnés à partir de cette composition |
| JP2002039448A (ja) * | 2000-07-19 | 2002-02-06 | Yokohama Rubber Co Ltd:The | 易滑り性高圧ホース |
| WO2003031543A2 (en) * | 2001-10-05 | 2003-04-17 | Unichema Chemie B.V. | Lubricant or fuel composition comprising an amide as friction-reducing additive |
| JP4117151B2 (ja) * | 2002-05-31 | 2008-07-16 | 日本カーバイド工業株式会社 | 難燃性シート |
| JP4005008B2 (ja) * | 2002-11-12 | 2007-11-07 | 花王株式会社 | ポリエステル系合成樹脂用添加剤 |
| US7267862B1 (en) | 2002-12-06 | 2007-09-11 | Appleton Papers Inc. | Controlled COF films |
| US20050232956A1 (en) * | 2004-02-26 | 2005-10-20 | Shailendra Bist | Method for separating saturated and unsaturated fatty acid esters and use of separated fatty acid esters |
| GB2412375A (en) | 2004-03-02 | 2005-09-28 | Croda Int Plc | Ester slip agents |
| MY143828A (en) * | 2004-06-17 | 2011-07-15 | Malaysian Palm Oil Board | A process for the production of fatty acid amides |
| US7678468B2 (en) | 2005-07-21 | 2010-03-16 | Chevron Phillips Chemicals Company Lp | Composition and method for the addition of saturated slip agents to multilayer polyethylene films |
| JP4813935B2 (ja) * | 2006-03-20 | 2011-11-09 | 上村工業株式会社 | 搬送用ハンガー |
| JP2008247972A (ja) * | 2007-03-29 | 2008-10-16 | Kaneka Corp | 熱可塑性樹脂組成物 |
-
2009
- 2009-06-23 GB GBGB0910781.4A patent/GB0910781D0/en not_active Ceased
-
2010
- 2010-06-18 CN CN201080028119.XA patent/CN102596895B/zh active Active
- 2010-06-18 JP JP2012516840A patent/JP2012530773A/ja active Pending
- 2010-06-18 WO PCT/GB2010/001197 patent/WO2010149952A2/en not_active Ceased
- 2010-06-18 EP EP10727486.2A patent/EP2445865B1/en active Active
- 2010-06-18 CA CA2763765A patent/CA2763765C/en active Active
- 2010-06-18 ES ES10727486.2T patent/ES2689426T3/es active Active
- 2010-06-18 US US13/380,445 patent/US8865809B2/en active Active
-
2014
- 2014-09-18 US US14/490,248 patent/US9328307B2/en active Active
-
2015
- 2015-09-28 JP JP2015189533A patent/JP6100855B2/ja active Active
Also Published As
| Publication number | Publication date |
|---|---|
| CA2763765A1 (en) | 2010-12-29 |
| US20150005211A1 (en) | 2015-01-01 |
| JP6100855B2 (ja) | 2017-03-22 |
| WO2010149952A3 (en) | 2012-04-19 |
| GB0910781D0 (en) | 2009-08-05 |
| ES2689426T3 (es) | 2018-11-14 |
| CN102596895A (zh) | 2012-07-18 |
| JP2016006122A (ja) | 2016-01-14 |
| US8865809B2 (en) | 2014-10-21 |
| CN102596895B (zh) | 2014-09-17 |
| EP2445865B1 (en) | 2018-08-08 |
| JP2012530773A (ja) | 2012-12-06 |
| US20120101201A1 (en) | 2012-04-26 |
| EP2445865A2 (en) | 2012-05-02 |
| US9328307B2 (en) | 2016-05-03 |
| WO2010149952A2 (en) | 2010-12-29 |
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Legal Events
| Date | Code | Title | Description |
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| EEER | Examination request |
Effective date: 20150309 |