CA1114973A - Substance de revetement antistatique a base de chlorure de vinylidene et pellicule ainsi couverte - Google Patents

Substance de revetement antistatique a base de chlorure de vinylidene et pellicule ainsi couverte

Info

Publication number: CA1114973A
Authority: CA; Canada
Prior art keywords: film; acid; composition; weight; vinylidene chloride
Prior art date: 1976-08-13
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

Application number

CA284,670A

Other languages

English (en)

Inventor

Clare W. Gerow

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

EIDP Inc

Original Assignee

EI Du Pont de Nemours and Co

Priority date (The priority date 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 date listed.)

1976-08-13

Filing date

1977-08-11

Publication date

1981-12-22

1977-05-20 Priority claimed from US05/799,123 external-priority patent/US4115334A/en

1977-08-11 Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co

1981-12-22 Application granted granted Critical

1981-12-22 Publication of CA1114973A publication Critical patent/CA1114973A/fr

Status Expired legal-status Critical Current

Links

239000008199 coating composition Substances 0.000 title claims abstract description 40
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 title claims description 21
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims abstract description 62
229920001577 copolymer Polymers 0.000 claims abstract description 43
-1 orthophosphoric acid Chemical compound 0.000 claims abstract description 32
235000011007 phosphoric acid Nutrition 0.000 claims abstract description 29
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims abstract description 27
229920000728 polyester Polymers 0.000 claims abstract description 21
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims abstract description 8
239000011574 phosphorus Substances 0.000 claims abstract description 8
229910052698 phosphorus Inorganic materials 0.000 claims abstract description 8
150000007519 polyprotic acids Polymers 0.000 claims abstract description 8
239000004627 regenerated cellulose Substances 0.000 claims abstract description 7
239000000203 mixture Substances 0.000 claims description 49
239000002253 acid Substances 0.000 claims description 18
229910000147 aluminium phosphate Inorganic materials 0.000 claims description 14
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 13
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 12
229920006267 polyester film Polymers 0.000 claims description 11
VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 claims description 10
UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 claims description 10
150000002895 organic esters Chemical class 0.000 claims description 10
239000000178 monomer Substances 0.000 claims description 9
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 8
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 8
LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 claims description 8
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 claims description 8
125000000217 alkyl group Chemical group 0.000 claims description 6
125000003118 aryl group Chemical group 0.000 claims description 6
125000004432 carbon atom Chemical group C* 0.000 claims description 6
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 6
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 claims description 6
229920001225 polyester resin Polymers 0.000 claims description 6
239000004645 polyester resin Substances 0.000 claims description 6
229920000139 polyethylene terephthalate Polymers 0.000 claims description 6
239000005020 polyethylene terephthalate Substances 0.000 claims description 6
ARIWANIATODDMH-UHFFFAOYSA-N rac-1-monolauroylglycerol Chemical compound CCCCCCCCCCCC(=O)OCC(O)CO ARIWANIATODDMH-UHFFFAOYSA-N 0.000 claims description 6
235000021357 Behenic acid Nutrition 0.000 claims description 5
229940116226 behenic acid Drugs 0.000 claims description 5
150000002009 diols Chemical class 0.000 claims description 5
229940075507 glyceryl monostearate Drugs 0.000 claims description 5
239000001788 mono and diglycerides of fatty acids Substances 0.000 claims description 5
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 4
229920000877 Melamine resin Polymers 0.000 claims description 4
125000002015 acyclic group Chemical group 0.000 claims description 4
239000001361 adipic acid Substances 0.000 claims description 4
235000011037 adipic acid Nutrition 0.000 claims description 4
229920003180 amino resin Polymers 0.000 claims description 4
239000004204 candelilla wax Substances 0.000 claims description 4
235000013868 candelilla wax Nutrition 0.000 claims description 4
229940073532 candelilla wax Drugs 0.000 claims description 4
239000004203 carnauba wax Substances 0.000 claims description 4
235000013869 carnauba wax Nutrition 0.000 claims description 4
239000007859 condensation product Substances 0.000 claims description 4
IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
229940037312 stearamide Drugs 0.000 claims description 4
NBIIXXVUZAFLBC-UHFFFAOYSA-L Phosphate ion(2-) Chemical compound OP([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-L 0.000 claims description 3
239000003795 chemical substances by application Substances 0.000 claims description 3
229940068939 glyceryl monolaurate Drugs 0.000 claims description 3
229910052736 halogen Inorganic materials 0.000 claims description 3
150000002367 halogens Chemical group 0.000 claims description 3
125000006353 oxyethylene group Chemical group 0.000 claims description 3
229920000058 polyacrylate Polymers 0.000 claims description 3
239000001993 wax Substances 0.000 claims description 3
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 2
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 claims description 2
238000004132 cross linking Methods 0.000 claims description 2
XPPKVPWEQAFLFU-UHFFFAOYSA-N diphosphoric acid Chemical compound OP(O)(=O)OP(O)(O)=O XPPKVPWEQAFLFU-UHFFFAOYSA-N 0.000 claims description 2
125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 claims description 2
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
229940005657 pyrophosphoric acid Drugs 0.000 claims description 2
ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 claims description 2
239000000306 component Substances 0.000 claims 20
230000001464 adherent effect Effects 0.000 claims 9
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 2
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 2
229910052794 bromium Inorganic materials 0.000 claims 2
229910052801 chlorine Inorganic materials 0.000 claims 2
239000000460 chlorine Substances 0.000 claims 2
125000001309 chloro group Chemical group Cl* 0.000 claims 2
239000011737 fluorine Chemical group 0.000 claims 2
229910052731 fluorine Inorganic materials 0.000 claims 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 claims 1
230000003068 static effect Effects 0.000 abstract description 8
239000010408 film Substances 0.000 description 51
238000000576 coating method Methods 0.000 description 24
239000011248 coating agent Substances 0.000 description 23
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 12
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
229960004838 phosphoric acid Drugs 0.000 description 11
238000007789 sealing Methods 0.000 description 10
125000005456 glyceride group Chemical group 0.000 description 8
238000012360 testing method Methods 0.000 description 8
150000002148 esters Chemical class 0.000 description 7
239000004698 Polyethylene Substances 0.000 description 6
239000000463 material Substances 0.000 description 6
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 6
230000004888 barrier function Effects 0.000 description 5
150000001875 compounds Chemical class 0.000 description 5
235000014786 phosphorus Nutrition 0.000 description 5
239000002904 solvent Substances 0.000 description 5
YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 3
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
125000001931 aliphatic group Chemical group 0.000 description 3
125000004122 cyclic group Chemical group 0.000 description 3
238000009472 formulation Methods 0.000 description 3
238000000034 method Methods 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 3
150000007522 mineralic acids Chemical class 0.000 description 3
238000004806 packaging method and process Methods 0.000 description 3
229920000573 polyethylene Polymers 0.000 description 3
229920000642 polymer Polymers 0.000 description 3
229920005989 resin Polymers 0.000 description 3
239000011347 resin Substances 0.000 description 3
239000007787 solid Substances 0.000 description 3
239000000758 substrate Substances 0.000 description 3
239000000454 talc Substances 0.000 description 3
229910052623 talc Inorganic materials 0.000 description 3
229920001634 Copolyester Polymers 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
229910019142 PO4 Inorganic materials 0.000 description 2
229920001283 Polyalkylene terephthalate Polymers 0.000 description 2
239000004743 Polypropylene Substances 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
229920006397 acrylic thermoplastic Polymers 0.000 description 2
238000004026 adhesive bonding Methods 0.000 description 2
125000005189 alkyl hydroxy group Chemical group 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
125000002511 behenyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
239000000470 constituent Substances 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-M dihydrogenphosphate Chemical compound OP(O)([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-M 0.000 description 2
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
238000001035 drying Methods 0.000 description 2
230000000694 effects Effects 0.000 description 2
FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 2
150000002334 glycols Chemical class 0.000 description 2
150000002431 hydrogen Chemical group 0.000 description 2
238000010030 laminating Methods 0.000 description 2
JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
235000021317 phosphate Nutrition 0.000 description 2
150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
150000003014 phosphoric acid esters Chemical class 0.000 description 2
229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
229920001155 polypropylene Polymers 0.000 description 2
239000000047 product Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 2
UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
NQPJDJVGBDHCAD-UHFFFAOYSA-N 1,3-diazinan-2-one Chemical compound OC1=NCCCN1 NQPJDJVGBDHCAD-UHFFFAOYSA-N 0.000 description 1
VOCDJQSAMZARGX-UHFFFAOYSA-N 1-ethenylpyrrolidine-2,5-dione Chemical compound C=CN1C(=O)CCC1=O VOCDJQSAMZARGX-UHFFFAOYSA-N 0.000 description 1
QHZLMUACJMDIAE-SFHVURJKSA-N 1-hexadecanoyl-sn-glycerol Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@@H](O)CO QHZLMUACJMDIAE-SFHVURJKSA-N 0.000 description 1
KUIZKZHDMPERHR-UHFFFAOYSA-N 1-phenylprop-2-en-1-one Chemical compound C=CC(=O)C1=CC=CC=C1 KUIZKZHDMPERHR-UHFFFAOYSA-N 0.000 description 1
IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
GPOGMJLHWQHEGF-UHFFFAOYSA-N 2-chloroethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCl GPOGMJLHWQHEGF-UHFFFAOYSA-N 0.000 description 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 description 1
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
238000003855 Adhesive Lamination Methods 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
PDQAZBWRQCGBEV-UHFFFAOYSA-N Ethylenethiourea Chemical compound S=C1NCCN1 PDQAZBWRQCGBEV-UHFFFAOYSA-N 0.000 description 1
YZCKVEUIGOORGS-UHFFFAOYSA-N Hydrogen atom Chemical compound [H] YZCKVEUIGOORGS-UHFFFAOYSA-N 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
QHZLMUACJMDIAE-UHFFFAOYSA-N Palmitic acid monoglyceride Natural products CCCCCCCCCCCCCCCC(=O)OCC(O)CO QHZLMUACJMDIAE-UHFFFAOYSA-N 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
229920001328 Polyvinylidene chloride Polymers 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
BWVAOONFBYYRHY-UHFFFAOYSA-N [4-(hydroxymethyl)phenyl]methanol Chemical compound OCC1=CC=C(CO)C=C1 BWVAOONFBYYRHY-UHFFFAOYSA-N 0.000 description 1
150000001252 acrylic acid derivatives Chemical class 0.000 description 1
230000002411 adverse Effects 0.000 description 1
150000001299 aldehydes Chemical class 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
229920000180 alkyd Polymers 0.000 description 1
125000005907 alkyl ester group Chemical group 0.000 description 1
229910000323 aluminium silicate Inorganic materials 0.000 description 1
239000002216 antistatic agent Substances 0.000 description 1
235000015173 baked goods and baking mixes Nutrition 0.000 description 1
230000005540 biological transmission Effects 0.000 description 1
INLLPKCGLOXCIV-UHFFFAOYSA-N bromoethene Chemical compound BrC=C INLLPKCGLOXCIV-UHFFFAOYSA-N 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
229940000425 combination drug Drugs 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
125000000853 cresyl group Chemical group C1(=CC=C(C=C1)C)* 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
IEPRKVQEAMIZSS-AATRIKPKSA-N diethyl fumarate Chemical compound CCOC(=O)\C=C\C(=O)OCC IEPRKVQEAMIZSS-AATRIKPKSA-N 0.000 description 1
ZWWQRMFIZFPUAA-UHFFFAOYSA-N dimethyl 2-methylidenebutanedioate Chemical compound COC(=O)CC(=C)C(=O)OC ZWWQRMFIZFPUAA-UHFFFAOYSA-N 0.000 description 1
239000002355 dual-layer Substances 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
230000032050 esterification Effects 0.000 description 1
238000005886 esterification reaction Methods 0.000 description 1
XJELOQYISYPGDX-UHFFFAOYSA-N ethenyl 2-chloroacetate Chemical compound ClCC(=O)OC=C XJELOQYISYPGDX-UHFFFAOYSA-N 0.000 description 1
UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000007765 extrusion coating Methods 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
239000007888 film coating Substances 0.000 description 1
238000009501 film coating Methods 0.000 description 1
235000013305 food Nutrition 0.000 description 1
235000011187 glycerol Nutrition 0.000 description 1
125000002818 heptacosyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical compound O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
235000013372 meat Nutrition 0.000 description 1
150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
239000002184 metal Substances 0.000 description 1
FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
AWJZTPWDQYFQPQ-UHFFFAOYSA-N methyl 2-chloroprop-2-enoate Chemical compound COC(=O)C(Cl)=C AWJZTPWDQYFQPQ-UHFFFAOYSA-N 0.000 description 1
239000003607 modifier Substances 0.000 description 1
KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 1
KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
229920000620 organic polymer Polymers 0.000 description 1
239000005022 packaging material Substances 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
229920002239 polyacrylonitrile Polymers 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
229920000647 polyepoxide Polymers 0.000 description 1
229920000137 polyphosphoric acid Polymers 0.000 description 1
229920000136 polysorbate Polymers 0.000 description 1
229920001343 polytetrafluoroethylene Polymers 0.000 description 1
239000004810 polytetrafluoroethylene Substances 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
239000005033 polyvinylidene chloride Substances 0.000 description 1
238000009824 pressure lamination Methods 0.000 description 1
238000003303 reheating Methods 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000003756 stirring Methods 0.000 description 1
SEEPANYCNGTZFQ-UHFFFAOYSA-N sulfadiazine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)NC1=NC=CC=N1 SEEPANYCNGTZFQ-UHFFFAOYSA-N 0.000 description 1
239000003760 tallow Substances 0.000 description 1
KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
239000010409 thin film Substances 0.000 description 1
238000005809 transesterification reaction Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/16—Anti-static materials
- 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

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Laminated Bodies (AREA)
Paints Or Removers (AREA)
Compositions Of Macromolecular Compounds (AREA)

CA284,670A 1976-08-13 1977-08-11 Substance de revetement antistatique a base de chlorure de vinylidene et pellicule ainsi couverte Expired CA1114973A (fr)

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
US71426876A	1976-08-13	1976-08-13
US714,268		1976-08-13
US05/799,123 US4115334A (en)	1976-08-13	1977-05-20	Antistatic vinylidene chloride coating composition, and film coated therewith
US799,123		1977-05-20

Publications (1)

Publication Number	Publication Date
CA1114973A true CA1114973A (fr)	1981-12-22

Family

ID=27109121

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA284,670A Expired CA1114973A (fr)	1976-08-13	1977-08-11	Substance de revetement antistatique a base de chlorure de vinylidene et pellicule ainsi couverte

Country Status (7)

Country	Link
JP (1)	JPS5323331A (fr)
CA (1)	CA1114973A (fr)
DE (1)	DE2736452A1 (fr)
FR (1)	FR2361451A1 (fr)
GB (1)	GB1571160A (fr)
LU (1)	LU77960A1 (fr)
NL (1)	NL7708932A (fr)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5017425A (fr) *	1973-06-08	1975-02-24
JPS53119919A (en) *	1977-03-28	1978-10-19	Kumagai Gumi Co Ltd	Manufacture of light weight foamed concrete having strengthened surface
JPS53119920A (en) *	1977-03-28	1978-10-19	Kumagai Gumi Co Ltd	Manufacture of wide width of light weight foamed concrete
JPS599005A (ja) *	1982-07-08	1984-01-18	小林ブロツク工業株式会社	断熱化粧ブロツクの成形方法
US4575838A (en) *	1984-02-29	1986-03-11	Rca Corporation	Sandwich-type capacitive electronic discs
DE3733182A1 (de) *	1987-10-01	1989-04-20	Hoechst Ag	Haertungskomponente und deren verwendung
US5225134A (en)	1991-02-08	1993-07-06	Concrete Design Specialties, Inc.	Methods of forming contoured walls
JP3523340B2 (ja) *	1994-08-30	2004-04-26	呉羽化学工業株式会社	塩化ビニリデン系重合体成形物
US5885502A (en) *	1995-12-20	1999-03-23	Bomanite Corporation	Method of forming patterned walls

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3341343A (en) *	1963-11-12	1967-09-12	Gen Anilline & Film Corp	Hydrophobic polymeric resin containing phosphate ester antistatic agent and process for producing antistatic properties
GB1267348A (en) *	1968-05-31	1972-03-15	Unilever Ltd	Antistatic resinous compositions
US3896066A (en) *	1973-05-02	1975-07-22	Du Pont	Vinylidene chloride coating composition containing an aromatic polyester and polyester substrates coated with the coating composition

1977
- 1977-08-11 CA CA284,670A patent/CA1114973A/fr not_active Expired
- 1977-08-11 GB GB3378877A patent/GB1571160A/en not_active Expired
- 1977-08-12 DE DE19772736452 patent/DE2736452A1/de not_active Withdrawn
- 1977-08-12 LU LU77960A patent/LU77960A1/xx unknown
- 1977-08-12 NL NL7708932A patent/NL7708932A/xx unknown
- 1977-08-12 JP JP9623077A patent/JPS5323331A/ja active Pending
- 1977-08-12 FR FR7724891A patent/FR2361451A1/fr active Granted

Also Published As

Publication number	Publication date
NL7708932A (nl)	1978-02-15
FR2361451A1 (fr)	1978-03-10
LU77960A1 (fr)	1978-04-27
DE2736452A1 (de)	1978-02-16
JPS5323331A (en)	1978-03-03
FR2361451B1 (fr)	1980-12-26
GB1571160A (en)	1980-07-09

Legal Events

Date	Code	Title	Description
1998-12-22	MKEX	Expiry

Publication	Publication Date	Title
US4115334A (en)	1978-09-19	Antistatic vinylidene chloride coating composition, and film coated therewith
CA1114973A (fr)	1981-12-22	Substance de revetement antistatique a base de chlorure de vinylidene et pellicule ainsi couverte
US5225288A (en)	1993-07-06	Solvent blockers and multilayer barrier coatings for thin films
FI81525B (fi)	1990-07-31	Vinylkloridpolymerlaminat.
JPS58167163A (ja)	1983-10-03	ヒ−トシ−ル性多層包装用配向フイルムおよびその製造方法
US5429867A (en)	1995-07-04	Synthetic hectorite coated flexible film
EP0027699B1 (fr)	1984-03-21	Procédé pour la production de pellicules thermoplastiques antistatiques et pellicules fabriquées selon ce procédé
GB2111857A (en)	1983-07-13	Heat-sealable polyolefin films and processes for their production
US3376246A (en)	1968-04-02	Polyvinyl chloride plastisols having greatly improved properties
US20190153180A1 (en)	2019-05-23	Film coating composition and method
US3297518A (en)	1967-01-10	Composite laminate film and method of making same
US5346755A (en)	1994-09-13	Stain resistant cleanable PVC fabric
US3222211A (en)	1965-12-07	Novel packaging films and processes therefor
US3896066A (en)	1975-07-22	Vinylidene chloride coating composition containing an aromatic polyester and polyester substrates coated with the coating composition
US3030325A (en)	1962-04-17	Coating composition comprising an aqueous emulsion of vinylidene chloride and amine-aldehyde resin, method of coating polystyrene therewith, and article thus coated
US4246319A (en)	1981-01-20	Coating for polyolefinic products and products covered by said coatings
US3958065A (en)	1976-05-18	Polyester film coated with a vinylidene chloride copolymer containing a linear polyester resin
US3874914A (en)	1975-04-01	Adhesive coatings of vinyl polymers and copolymers and method of making same
US3128200A (en)	1964-04-07	Coated alkenyl aromatic article and method of coating
US3684564A (en)	1972-08-15	Heat sealable elements
US4229327A (en)	1980-10-21	Coatings for polyolefinic products and products covered by skid coatings
US3397079A (en)	1968-08-13	Heat-sealable polyolefin film coated with a plasticized vinylidene chloride copolymer
US3985920A (en)	1976-10-12	Adhesive coating of vinyl polymers and copolymers and method of making same
JP2023164510A (ja)	2023-11-10	保香性包装袋用積層体及び包装袋
US3975573A (en)	1976-08-17	Polyester film coated with an inorganic coating and with a vinylidene chloride copolymer containing a linear polyester resin