JP5912157B2 - ポリ塩化ビニル組成物 - Google Patents
ポリ塩化ビニル組成物 Download PDFInfo
- Publication number
- JP5912157B2 JP5912157B2 JP2014184207A JP2014184207A JP5912157B2 JP 5912157 B2 JP5912157 B2 JP 5912157B2 JP 2014184207 A JP2014184207 A JP 2014184207A JP 2014184207 A JP2014184207 A JP 2014184207A JP 5912157 B2 JP5912157 B2 JP 5912157B2
- Authority
- JP
- Japan
- Prior art keywords
- phthalate
- plasticizer
- acid
- adipate
- ethylhexyl
- 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.)
- Active
Links
- 239000000203 mixture Substances 0.000 title claims description 141
- 239000004800 polyvinyl chloride Substances 0.000 title claims description 77
- 229920000915 polyvinyl chloride Polymers 0.000 title claims description 74
- 239000004014 plasticizer Substances 0.000 claims description 82
- 229920005989 resin Polymers 0.000 claims description 46
- 239000011347 resin Substances 0.000 claims description 46
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 claims description 41
- 238000002844 melting Methods 0.000 claims description 26
- 230000008018 melting Effects 0.000 claims description 26
- LQLQDKBJAIILIQ-UHFFFAOYSA-N Dibutyl terephthalate Chemical group CCCCOC(=O)C1=CC=C(C(=O)OCCCC)C=C1 LQLQDKBJAIILIQ-UHFFFAOYSA-N 0.000 claims description 25
- 239000003381 stabilizer Substances 0.000 claims description 25
- IRIAEXORFWYRCZ-UHFFFAOYSA-N Butylbenzyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-UHFFFAOYSA-N 0.000 claims description 21
- -1 undecyl dodecyl Chemical group 0.000 claims description 20
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 claims description 19
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 claims description 17
- 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 claims description 15
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 13
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 12
- 239000002253 acid Substances 0.000 claims description 12
- 125000005498 phthalate group Chemical class 0.000 claims description 12
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 11
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 claims description 11
- KCXZNSGUUQJJTR-UHFFFAOYSA-N Di-n-hexyl phthalate Chemical compound CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCC KCXZNSGUUQJJTR-UHFFFAOYSA-N 0.000 claims description 10
- DAFHKNAQFPVRKR-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylpropanoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)C DAFHKNAQFPVRKR-UHFFFAOYSA-N 0.000 claims description 8
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 claims description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 8
- ZFOZVQLOBQUTQQ-UHFFFAOYSA-N Tributyl citrate Chemical compound CCCCOC(=O)CC(O)(C(=O)OCCCC)CC(=O)OCCCC ZFOZVQLOBQUTQQ-UHFFFAOYSA-N 0.000 claims description 8
- MGWAVDBGNNKXQV-UHFFFAOYSA-N diisobutyl phthalate Chemical compound CC(C)COC(=O)C1=CC=CC=C1C(=O)OCC(C)C MGWAVDBGNNKXQV-UHFFFAOYSA-N 0.000 claims description 8
- 229920000728 polyester Polymers 0.000 claims description 8
- XFDQLDNQZFOAFK-UHFFFAOYSA-N 2-benzoyloxyethyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCCOC(=O)C1=CC=CC=C1 XFDQLDNQZFOAFK-UHFFFAOYSA-N 0.000 claims description 7
- CAZKHBNCZSWFFM-UHFFFAOYSA-N 2-undecoxycarbonylbenzoic acid Chemical compound CCCCCCCCCCCOC(=O)C1=CC=CC=C1C(O)=O CAZKHBNCZSWFFM-UHFFFAOYSA-N 0.000 claims description 7
- UMVMVEZHMZTUHD-UHFFFAOYSA-N DL-Propylene glycol dibenzoate Chemical compound C=1C=CC=CC=1C(=O)OC(C)COC(=O)C1=CC=CC=C1 UMVMVEZHMZTUHD-UHFFFAOYSA-N 0.000 claims description 7
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 claims description 7
- 229960002380 dibutyl phthalate Drugs 0.000 claims description 7
- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 claims description 7
- 239000002245 particle Substances 0.000 claims description 7
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 6
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 claims description 6
- 239000000843 powder Substances 0.000 claims description 6
- ZVFDTKUVRCTHQE-UHFFFAOYSA-N Diisodecyl phthalate Chemical compound CC(C)CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC(C)C ZVFDTKUVRCTHQE-UHFFFAOYSA-N 0.000 claims description 5
- YCZJVRCZIPDYHH-UHFFFAOYSA-N ditridecyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCCCCCC YCZJVRCZIPDYHH-UHFFFAOYSA-N 0.000 claims description 5
- XNGIFLGASWRNHJ-UHFFFAOYSA-N o-dicarboxybenzene Natural products OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 5
- 229920000642 polymer Polymers 0.000 claims description 5
- FTSXVYQZLNPTCM-UHFFFAOYSA-N (3-benzoyloxy-2,2,4-trimethylpentyl) benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC(C)(C)C(C(C)C)OC(=O)C1=CC=CC=C1 FTSXVYQZLNPTCM-UHFFFAOYSA-N 0.000 claims description 4
- DYJIIMFHSZKBDY-UHFFFAOYSA-N (3-benzoyloxy-2,2-dimethylpropyl) benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC(C)(C)COC(=O)C1=CC=CC=C1 DYJIIMFHSZKBDY-UHFFFAOYSA-N 0.000 claims description 4
- BHKLONWXRPJNAE-UHFFFAOYSA-N 1-o-butyl 2-o-cyclohexyl benzene-1,2-dicarboxylate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OC1CCCCC1 BHKLONWXRPJNAE-UHFFFAOYSA-N 0.000 claims description 4
- ACBFJMAXNZVRRX-UHFFFAOYSA-N 1-o-nonyl 2-o-undecyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCC ACBFJMAXNZVRRX-UHFFFAOYSA-N 0.000 claims description 4
- AHSGHEXYEABOKT-UHFFFAOYSA-N 2-[2-(2-benzoyloxyethoxy)ethoxy]ethyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCCOCCOCCOC(=O)C1=CC=CC=C1 AHSGHEXYEABOKT-UHFFFAOYSA-N 0.000 claims description 4
- LUNMJRJMSXZSLC-UHFFFAOYSA-N 2-cyclopropylethanol Chemical compound OCCC1CC1 LUNMJRJMSXZSLC-UHFFFAOYSA-N 0.000 claims description 4
- UADWUILHKRXHMM-UHFFFAOYSA-N 2-ethylhexyl benzoate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1 UADWUILHKRXHMM-UHFFFAOYSA-N 0.000 claims description 4
- 229940106004 2-ethylhexyl benzoate Drugs 0.000 claims description 4
- ALKCLFLTXBBMMP-UHFFFAOYSA-N 3,7-dimethylocta-1,6-dien-3-yl hexanoate Chemical compound CCCCCC(=O)OC(C)(C=C)CCC=C(C)C ALKCLFLTXBBMMP-UHFFFAOYSA-N 0.000 claims description 4
- SIXWIUJQBBANGK-UHFFFAOYSA-N 4-(4-fluorophenyl)-1h-pyrazol-5-amine Chemical compound N1N=CC(C=2C=CC(F)=CC=2)=C1N SIXWIUJQBBANGK-UHFFFAOYSA-N 0.000 claims description 4
- DMIMWGHYIPFAIF-UHFFFAOYSA-N 5-nitro-2-piperidin-1-ylaniline Chemical compound NC1=CC([N+]([O-])=O)=CC=C1N1CCCCC1 DMIMWGHYIPFAIF-UHFFFAOYSA-N 0.000 claims description 4
- BBVARVTURNYWGV-UHFFFAOYSA-N 7-methyloctyl benzoate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1 BBVARVTURNYWGV-UHFFFAOYSA-N 0.000 claims description 4
- 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 claims description 4
- 239000004803 Di-2ethylhexylphthalate Substances 0.000 claims description 4
- 239000004641 Diallyl-phthalate Substances 0.000 claims description 4
- PYGXAGIECVVIOZ-UHFFFAOYSA-N Dibutyl decanedioate Chemical compound CCCCOC(=O)CCCCCCCCC(=O)OCCCC PYGXAGIECVVIOZ-UHFFFAOYSA-N 0.000 claims description 4
- VOWAEIGWURALJQ-UHFFFAOYSA-N Dicyclohexyl phthalate Chemical compound C=1C=CC=C(C(=O)OC2CCCCC2)C=1C(=O)OC1CCCCC1 VOWAEIGWURALJQ-UHFFFAOYSA-N 0.000 claims description 4
- HIZCTWCPHWUPFU-UHFFFAOYSA-N Glycerol tribenzoate Chemical compound C=1C=CC=CC=1C(=O)OCC(OC(=O)C=1C=CC=CC=1)COC(=O)C1=CC=CC=C1 HIZCTWCPHWUPFU-UHFFFAOYSA-N 0.000 claims description 4
- 229910019142 PO4 Inorganic materials 0.000 claims description 4
- MURWRBWZIMXKGC-UHFFFAOYSA-N Phthalsaeure-butylester-octylester Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC MURWRBWZIMXKGC-UHFFFAOYSA-N 0.000 claims description 4
- 239000001361 adipic acid Substances 0.000 claims description 4
- 235000011037 adipic acid Nutrition 0.000 claims description 4
- UADWUILHKRXHMM-ZDUSSCGKSA-N benzoflex 181 Natural products CCCC[C@H](CC)COC(=O)C1=CC=CC=C1 UADWUILHKRXHMM-ZDUSSCGKSA-N 0.000 claims description 4
- KZBSIGKPGIZQJQ-UHFFFAOYSA-N bis(2-butoxyethyl) decanedioate Chemical compound CCCCOCCOC(=O)CCCCCCCCC(=O)OCCOCCCC KZBSIGKPGIZQJQ-UHFFFAOYSA-N 0.000 claims description 4
- IHTSDBYPAZEUOP-UHFFFAOYSA-N bis(2-butoxyethyl) hexanedioate Chemical compound CCCCOCCOC(=O)CCCCC(=O)OCCOCCCC IHTSDBYPAZEUOP-UHFFFAOYSA-N 0.000 claims description 4
- SAOKZLXYCUGLFA-UHFFFAOYSA-N bis(2-ethylhexyl) adipate Chemical compound CCCCC(CC)COC(=O)CCCCC(=O)OCC(CC)CCCC SAOKZLXYCUGLFA-UHFFFAOYSA-N 0.000 claims description 4
- ZFMQKOWCDKKBIF-UHFFFAOYSA-N bis(3,5-difluorophenyl)phosphane Chemical compound FC1=CC(F)=CC(PC=2C=C(F)C=C(F)C=2)=C1 ZFMQKOWCDKKBIF-UHFFFAOYSA-N 0.000 claims description 4
- CJFLBOQMPJCWLR-UHFFFAOYSA-N bis(6-methylheptyl) hexanedioate Chemical compound CC(C)CCCCCOC(=O)CCCCC(=O)OCCCCCC(C)C CJFLBOQMPJCWLR-UHFFFAOYSA-N 0.000 claims description 4
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 claims description 4
- 239000004359 castor oil Substances 0.000 claims description 4
- 235000019438 castor oil Nutrition 0.000 claims description 4
- 239000007795 chemical reaction product Substances 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- UCVPKAZCQPRWAY-UHFFFAOYSA-N dibenzyl benzene-1,2-dicarboxylate Chemical compound C=1C=CC=C(C(=O)OCC=2C=CC=CC=2)C=1C(=O)OCC1=CC=CC=C1 UCVPKAZCQPRWAY-UHFFFAOYSA-N 0.000 claims description 4
- JQCXWCOOWVGKMT-UHFFFAOYSA-N diheptyl phthalate Chemical compound CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC JQCXWCOOWVGKMT-UHFFFAOYSA-N 0.000 claims description 4
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 claims description 4
- 229960001826 dimethylphthalate Drugs 0.000 claims description 4
- DROMNWUQASBTFM-UHFFFAOYSA-N dinonyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCC DROMNWUQASBTFM-UHFFFAOYSA-N 0.000 claims description 4
- OEIWPNWSDYFMIL-UHFFFAOYSA-N dioctyl benzene-1,4-dicarboxylate Chemical compound CCCCCCCCOC(=O)C1=CC=C(C(=O)OCCCCCCCC)C=C1 OEIWPNWSDYFMIL-UHFFFAOYSA-N 0.000 claims description 4
- XWVQUJDBOICHGH-UHFFFAOYSA-N dioctyl nonanedioate Chemical compound CCCCCCCCOC(=O)CCCCCCCC(=O)OCCCCCCCC XWVQUJDBOICHGH-UHFFFAOYSA-N 0.000 claims description 4
- VJHINFRRDQUWOJ-UHFFFAOYSA-N dioctyl sebacate Chemical compound CCCCC(CC)COC(=O)CCCCCCCCC(=O)OCC(CC)CCCC VJHINFRRDQUWOJ-UHFFFAOYSA-N 0.000 claims description 4
- LZJUZSYHFSVIGJ-UHFFFAOYSA-N ditridecyl hexanedioate Chemical compound CCCCCCCCCCCCCOC(=O)CCCCC(=O)OCCCCCCCCCCCCC LZJUZSYHFSVIGJ-UHFFFAOYSA-N 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 4
- JFCQEDHGNNZCLN-UHFFFAOYSA-N glutaric acid Chemical compound OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 claims description 4
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 claims description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 4
- 125000001400 nonyl 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])[H] 0.000 claims description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 4
- 239000010452 phosphate Substances 0.000 claims description 4
- 229920000151 polyglycol Polymers 0.000 claims description 4
- 239000010695 polyglycol Substances 0.000 claims description 4
- 229940116351 sebacate Drugs 0.000 claims description 4
- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 claims description 4
- WEAPVABOECTMGR-UHFFFAOYSA-N triethyl 2-acetyloxypropane-1,2,3-tricarboxylate Chemical compound CCOC(=O)CC(C(=O)OCC)(OC(C)=O)CC(=O)OCC WEAPVABOECTMGR-UHFFFAOYSA-N 0.000 claims description 4
- GWVUTNGDMGTPFE-UHFFFAOYSA-N trihexyl 2-butanoyloxypropane-1,2,3-tricarboxylate Chemical compound CCCCCCOC(=O)CC(C(=O)OCCCCCC)(OC(=O)CCC)CC(=O)OCCCCCC GWVUTNGDMGTPFE-UHFFFAOYSA-N 0.000 claims description 4
- HORIEOQXBKUKGQ-UHFFFAOYSA-N bis(7-methyloctyl) cyclohexane-1,2-dicarboxylate Chemical compound CC(C)CCCCCCOC(=O)C1CCCCC1C(=O)OCCCCCCC(C)C HORIEOQXBKUKGQ-UHFFFAOYSA-N 0.000 claims description 3
- RLRMXWDXPLINPJ-UHFFFAOYSA-N dioctan-2-yl benzene-1,2-dicarboxylate Chemical compound CCCCCCC(C)OC(=O)C1=CC=CC=C1C(=O)OC(C)CCCCCC RLRMXWDXPLINPJ-UHFFFAOYSA-N 0.000 claims description 3
- QQVHEQUEHCEAKS-UHFFFAOYSA-N diundecyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCCCC QQVHEQUEHCEAKS-UHFFFAOYSA-N 0.000 claims description 3
- UWNADWZGEHDQAB-UHFFFAOYSA-N i-Pr2C2H4i-Pr2 Natural products CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 claims description 3
- 125000002347 octyl 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])[H] 0.000 claims description 3
- 238000006116 polymerization reaction Methods 0.000 claims description 3
- 229920001451 polypropylene glycol Polymers 0.000 claims description 3
- TUUQISRYLMFKOG-UHFFFAOYSA-N trihexyl 2-acetyloxypropane-1,2,3-tricarboxylate Chemical compound CCCCCCOC(=O)CC(C(=O)OCCCCCC)(OC(C)=O)CC(=O)OCCCCCC TUUQISRYLMFKOG-UHFFFAOYSA-N 0.000 claims description 3
- GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 claims description 3
- XBXNPIGUSWUOFT-UHFFFAOYSA-N 2-(2-propylheptoxycarbonyl)benzoic acid Chemical compound CCCCCC(CCC)COC(=O)C1=CC=CC=C1C(O)=O XBXNPIGUSWUOFT-UHFFFAOYSA-N 0.000 claims description 2
- 239000003963 antioxidant agent Substances 0.000 claims description 2
- 239000002216 antistatic agent Substances 0.000 claims description 2
- 125000002704 decyl 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])* 0.000 claims description 2
- 239000003063 flame retardant Substances 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 239000003112 inhibitor Substances 0.000 claims description 2
- 239000004611 light stabiliser Substances 0.000 claims description 2
- 239000000049 pigment Substances 0.000 claims description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims 19
- YPDXSCXISVYHOB-UHFFFAOYSA-N tris(7-methyloctyl) benzene-1,2,4-tricarboxylate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=C(C(=O)OCCCCCCC(C)C)C(C(=O)OCCCCCCC(C)C)=C1 YPDXSCXISVYHOB-UHFFFAOYSA-N 0.000 claims 1
- 239000004593 Epoxy Chemical class 0.000 description 26
- LQKWPGAPADIOSS-UHFFFAOYSA-N bis(2-methylpropyl) benzene-1,4-dicarboxylate Chemical compound CC(C)COC(=O)C1=CC=C(C(=O)OCC(C)C)C=C1 LQKWPGAPADIOSS-UHFFFAOYSA-N 0.000 description 18
- 239000003549 soybean oil Substances 0.000 description 15
- 235000012424 soybean oil Nutrition 0.000 description 15
- 229920001944 Plastisol Polymers 0.000 description 14
- 239000004999 plastisol Substances 0.000 description 14
- 230000000052 comparative effect Effects 0.000 description 12
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 12
- AGXUVMPSUKZYDT-UHFFFAOYSA-L barium(2+);octadecanoate Chemical compound [Ba+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O AGXUVMPSUKZYDT-UHFFFAOYSA-L 0.000 description 11
- 150000001875 compounds Chemical class 0.000 description 11
- 229910052751 metal Inorganic materials 0.000 description 11
- 239000002184 metal Substances 0.000 description 11
- 230000000704 physical effect Effects 0.000 description 9
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 7
- 239000008116 calcium stearate Substances 0.000 description 7
- 235000013539 calcium stearate Nutrition 0.000 description 7
- 238000002156 mixing Methods 0.000 description 7
- GWOWVOYJLHSRJJ-UHFFFAOYSA-L cadmium stearate Chemical compound [Cd+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O GWOWVOYJLHSRJJ-UHFFFAOYSA-L 0.000 description 6
- 238000011109 contamination Methods 0.000 description 6
- 239000000178 monomer Substances 0.000 description 6
- 239000000344 soap Substances 0.000 description 6
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical class OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 239000000976 ink Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000007614 solvation Methods 0.000 description 3
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 206010047289 Ventricular extrasystoles Diseases 0.000 description 2
- CVPZXHCZKMFVOZ-UHFFFAOYSA-N [4-(benzoyloxymethyl)cyclohexyl]methyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC(CC1)CCC1COC(=O)C1=CC=CC=C1 CVPZXHCZKMFVOZ-UHFFFAOYSA-N 0.000 description 2
- 238000003490 calendering Methods 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- OMSUIQOIVADKIM-UHFFFAOYSA-N ethyl 3-hydroxybutyrate Chemical compound CCOC(=O)CC(C)O OMSUIQOIVADKIM-UHFFFAOYSA-N 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- 238000009408 flooring Methods 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- PZTAGFCBNDBBFZ-UHFFFAOYSA-N tert-butyl 2-(hydroxymethyl)piperidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCCCC1CO PZTAGFCBNDBBFZ-UHFFFAOYSA-N 0.000 description 2
- WCLDITPGPXSPGV-UHFFFAOYSA-N tricamba Chemical compound COC1=C(Cl)C=C(Cl)C(Cl)=C1C(O)=O WCLDITPGPXSPGV-UHFFFAOYSA-N 0.000 description 2
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 2
- JHPBZFOKBAGZBL-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylprop-2-enoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)=C JHPBZFOKBAGZBL-UHFFFAOYSA-N 0.000 description 1
- ZBBLRPRYYSJUCZ-GRHBHMESSA-L (z)-but-2-enedioate;dibutyltin(2+) Chemical compound [O-]C(=O)\C=C/C([O-])=O.CCCC[Sn+2]CCCC ZBBLRPRYYSJUCZ-GRHBHMESSA-L 0.000 description 1
- OMVSWZDEEGIJJI-UHFFFAOYSA-N 2,2,4-Trimethyl-1,3-pentadienol diisobutyrate Chemical compound CC(C)C(=O)OC(C(C)C)C(C)(C)COC(=O)C(C)C OMVSWZDEEGIJJI-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- HNDYULRADYGBDU-UHFFFAOYSA-N 8-methylnonyl benzoate Chemical compound CC(C)CCCCCCCOC(=O)C1=CC=CC=C1 HNDYULRADYGBDU-UHFFFAOYSA-N 0.000 description 1
- LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 description 1
- OSLLZBMBYCIAPH-UHFFFAOYSA-N C(C(C)C)(=O)OCC(C(C(C)C)(OC(C(C)C)=O)C)C Chemical compound C(C(C)C)(=O)OCC(C(C(C)C)(OC(C(C)C)=O)C)C OSLLZBMBYCIAPH-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 229920012485 Plasticized Polyvinyl chloride Polymers 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- DOOTYTYQINUNNV-UHFFFAOYSA-N Triethyl citrate Chemical compound CCOC(=O)CC(O)(C(=O)OCC)CC(=O)OCC DOOTYTYQINUNNV-UHFFFAOYSA-N 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
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 239000013466 adhesive and sealant Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- RAKMKCZMVZBODU-PIQLPZBWSA-L barium(2+);(z)-12-hydroxyoctadec-9-enoate Chemical compound [Ba+2].CCCCCCC(O)C\C=C/CCCCCCCC([O-])=O.CCCCCCC(O)C\C=C/CCCCCCCC([O-])=O RAKMKCZMVZBODU-PIQLPZBWSA-L 0.000 description 1
- OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 1
- 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 1
- HIAAVKYLDRCDFQ-UHFFFAOYSA-L calcium;dodecanoate Chemical compound [Ca+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O HIAAVKYLDRCDFQ-UHFFFAOYSA-L 0.000 description 1
- ZCZLQYAECBEUBH-UHFFFAOYSA-L calcium;octadec-9-enoate Chemical compound [Ca+2].CCCCCCCCC=CCCCCCCCC([O-])=O.CCCCCCCCC=CCCCCCCCC([O-])=O ZCZLQYAECBEUBH-UHFFFAOYSA-L 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- PBAYDYUZOSNJGU-UHFFFAOYSA-N chelidonic acid Natural products OC(=O)C1=CC(=O)C=C(C(O)=O)O1 PBAYDYUZOSNJGU-UHFFFAOYSA-N 0.000 description 1
- 239000013626 chemical specie Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000006071 cream Substances 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
- GLOQRSIADGSLRX-UHFFFAOYSA-N decyl diphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OCCCCCCCCCC)OC1=CC=CC=C1 GLOQRSIADGSLRX-UHFFFAOYSA-N 0.000 description 1
- SZLIWAKTUJFFNX-UHFFFAOYSA-N dihydrocitronellol benzoate Natural products CC(C)CCCC(C)CCOC(=O)C1=CC=CC=C1 SZLIWAKTUJFFNX-UHFFFAOYSA-N 0.000 description 1
- PYBNTRWJKQJDRE-UHFFFAOYSA-L dodecanoate;tin(2+) Chemical compound [Sn+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O PYBNTRWJKQJDRE-UHFFFAOYSA-L 0.000 description 1
- QPMJENKZJUFOON-PLNGDYQASA-N ethyl (z)-3-chloro-2-cyano-4,4,4-trifluorobut-2-enoate Chemical compound CCOC(=O)C(\C#N)=C(/Cl)C(F)(F)F QPMJENKZJUFOON-PLNGDYQASA-N 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000011872 intimate mixture Substances 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000010309 melting process Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- AXRSHKZFNKUGQB-UHFFFAOYSA-N octyl diphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OCCCCCCCC)OC1=CC=CC=C1 AXRSHKZFNKUGQB-UHFFFAOYSA-N 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 238000012667 polymer degradation Methods 0.000 description 1
- 229920001290 polyvinyl ester Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000008117 stearic acid 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
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000001069 triethyl citrate Substances 0.000 description 1
- VMYFZRTXGLUXMZ-UHFFFAOYSA-N triethyl citrate Natural products CCOC(=O)C(O)(C(=O)OCC)C(=O)OCC VMYFZRTXGLUXMZ-UHFFFAOYSA-N 0.000 description 1
- 235000013769 triethyl citrate Nutrition 0.000 description 1
- CNUJLMSKURPSHE-UHFFFAOYSA-N trioctadecyl phosphite Chemical compound CCCCCCCCCCCCCCCCCCOP(OCCCCCCCCCCCCCCCCCC)OCCCCCCCCCCCCCCCCCC CNUJLMSKURPSHE-UHFFFAOYSA-N 0.000 description 1
- 125000002948 undecyl 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])[H] 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- CHJMFFKHPHCQIJ-UHFFFAOYSA-L zinc;octanoate Chemical compound [Zn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O CHJMFFKHPHCQIJ-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/092—Polycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/12—Esters; Ether-esters of cyclic polycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/15—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
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Footwear And Its Accessory, Manufacturing Method And Apparatuses (AREA)
- Cosmetics (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Paints Or Removers (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Organic Insulating Materials (AREA)
- Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Sealing Material Composition (AREA)
Description
上記の手順を使用し、2種の組成物を、PVC(Oxychem社によって供給されたOxy75HC樹脂)、70PHRの可塑剤、2PHRのエポキシ化大豆油(Crompton-Witco社によって供給されたDrapex6.8)及び2PHRの混合金属安定剤(Akros Chemicals社によって供給されたAkcrostabLT4798)から製造した。第一の組成物においては、可塑剤は、ジオクタルテレフタレート(DOTP)及びDBTPの重量基準で75:25のブレンドであった(実施例1)。第二の組成物に於いては、可塑剤は、DOTP及びジエチレングリコールジベンゾエートの重量基準で75:25のブレンドであった(比較例C−1)。
上記の手順を使用し、3種の組成物を、2種の異なったPVCの重量基準で70:30の混合物、即ち70部のOxy6547樹脂及び30部のOxy625樹脂、70PHRの可塑剤、3PHRのエポキシ化大豆油(Drapex6.8)及び2PHRの混合金属安定剤(Acros Chemical社によって供給されたAkcrostab4398)から製造した。Oxy230PVC粉末は、0.95の内部粘度(internal viscosity)IV及び68の分子量係数Kを有する。第一の組成物に於いて、可塑剤はDBTPであり(実施例2)、第二の組成物に於いて、可塑剤はジエチレングリコールジベンゾエートであり(比較例C−2)、第三の組成物に於いて、可塑剤はフタル酸ブチルベンジルであった(比較例C−3)。
上記の手順を使用し、2種の組成物を、2種の異なったPVCの重量基準で80:20の混合物、即ち80部のOxy75HC樹脂及び20部のOxy625樹脂、60PHRの可塑剤、3PHRのエポキシ化大豆油(Drapex6.8)及び2PHRの混合金属安定剤(Akrostab4398)から製造した。第一組成物に於いて、可塑剤はDBTPであり(実施例3)、第二組成物に於いて、可塑剤はフタル酸ブチルベンジルであった(比較例C−4)。
上記の手順を使用し、3種の組成物を、PVC樹脂(Oxy240F)、50PHRの可塑剤、2PHRのエポキシ化大豆油(Drapex6.8)及び2PHRの混合金属安定剤(AcrossLT4798)から製造した。第一の組成物に於いて、可塑剤は、DOTP及びジエチレングリコールジベンゾエート(Velsicol社からのBenzoflex2−45)であり(比較例C−5)、第二の組成物に於いて、可塑剤は、DOTP及びDBTPの75:25ブレンドであり(実施例4)、第三の組成物に於いて、可塑剤はDOTP及びDIBTPの75:25ブレンドであった(実施例5)。
上記の手順を使用し、3種の組成物を、91.4重量部のOxy80HC PVC及び8.6重量部のPVCブレンド樹脂Oxy567(共に、Oxychem社から供給された)からなるPVC樹脂のブレンド、30PHRの可塑剤、17PHRのTXIB(2,3,4−トリメチル−1,3−ペンタンジオールジイソブチレート)、8PHRのミネラルスピリット、3PHRのポリ(エチレングリコール)400及び5PHRの混合金属安定剤(Akrostab4798)から製造した。第一の組成物に於いて、可塑剤は混合ベンゾエート可塑剤ブレンド(Velsicol社からのBenzoflex6000)であり(比較例C−6)、第二の組成物に於いて、可塑剤はフタル酸ブチルベンジル(Ferro社によって供給されたSanticizer160)であり(比較例C−7)、第三の組成物に於いて、可塑剤はDBTPであった(実施例6)。プラスチゾルを508ミクロン(20ミル)金型内に入れ、そしてオーブン内で20.4℃(400°F)で2分間融解した。
態様1.ポリ塩化ビニル(PVC)樹脂と、テレフタル酸ジブチル、テレフタル酸ジイソブチル及びそれらの混合物からなる群から選択された可塑剤との混合物を含んでなるポリ塩化ビニル組成物。
態様2.前記組成物中の可塑剤の量がPVC樹脂100部当り可塑剤20〜800部である態様1に記載のPVC組成物。
態様3.前記組成物中の可塑剤の量がPVC樹脂100部当り可塑剤40〜120部である態様2に記載のPVC組成物。
態様4.フタル酸ジオクチル、フタル酸ジ−2−エチルヘキシル、フタル酸ジイソオクチル、フタル酸ジイソノニル、フタル酸ジ−線状ノニル、ジ−線状ノニル、ウンデシルフタレート、フタル酸ジ−線状ウンデシル、フタル酸ジウンデシル、フタル酸ジイソデシル、C6−C10線状フタレート、C7線状フタレート、C9線状フタレート、C11線状フタレート、フタル酸ジトリデシル、フタル酸ウンデシルドデシル、ジ(フタル酸2−プロピルヘプチル)、フタル酸ノニルウンデシル、フタル酸テキサノールベンジル、ポリエステルフタレート、フタル酸ジアリル、n−ブチルフタリル−n−ブチルグリコセート、フタル酸ジカプリル、フタル酸ブチルシクロヘキシル、フタル酸ジシクロヘキシル、フタル酸ブチルオクチル、テレフタル酸ジオクチル、テレフタル酸ジ−2−エチルヘキシル、アジピン酸ジオクチル、アジピン酸ジ−2−エチルヘキシル、アジピン酸ジイソニル、アジピン酸ジイソオクチル、アジピン酸ジイソデシル、アジピン酸ジトリデシル、アジピン酸ジブトキシエチル、アジピン酸ジブトキシエトキシ、アジピン酸ジ(nオクチル,nデシル)、ポリエステルアジペート、ポリグリコールアジペート、トリメリト酸トリオクチル、トリメリト酸トリ−2−エチルヘキシル、トリメリト酸トリイソオクチル、トリメリト酸トリイソノニル、トリメリト酸トリイソデシル、トリメリト酸トリ−n−ヘキシル、アゼライン酸ジオクチル、グルタル酸ジ−2−エチルヘキシル、セバシン酸ジ−2−エチルヘキシル、セバシン酸ジブチル、セバシン酸ジブトキシエチル、クエン酸トリエチル、クエン酸アセチルトリエチル、クエン酸トリ−n−ブチル、クエン酸アセチルトリ−n−ブチル、クエン酸アセチルトリ−n−ヘキシル、クエン酸n−ブチルトリ−n−ヘキシル、安息香酸イソノニル、安息香酸イソデシル、1,4−シクロヘキサンジメタノールジベンゾエート、2,2,4−トリメチル−1,3−ペンタンジオールジベンゾエート、2,2−ジメチル−1,3−プロパンジオールジベンゾエート、C10−C21アルカンフェノールエステル又はアルキルスルホン酸フェノールエステル、完全硬化ひまし油との酢酸反応生成物、ペンタエリスリトールテトラベンゾエート、グリセロールトリベンゾエート、ポリプロピレングリコールジベンゾエート、トリアリールホスフェート、ジイソノニルシクロヘキサン−1,2−ジカルボキシレート、グリコールとのアジピン酸/フタレート/アジペート/セバケートのポリマー及びしばしば酸末端のもの、フタル酸ブチルベンジル、フタル酸アルキルベンジル、フタル酸C7−C9ブチル、ジエチレングリコールジベンゾエート、ジプロピレングリコールジベンゾエート、安息香酸2−エチルヘキシル、安息香酸テキサノール、エチレングリコールジベンゾエート、プロピレングリコールジベンゾエート、トリエチレングリコールジベンゾエート、フタル酸ジ−ヘプチル、フタル酸ジヘキシル、フタル酸ジメチル、フタル酸ジエチル、フタル酸ジブチル、フタル酸ジイソブチル並びにこれらの混合物からなる群から選択された追加の可塑剤を更に含み、該可塑剤の10〜100重量%が、テレフタル酸ジブチル、テレフタル酸ジイソブチル又はそれらの混合物である態様2に記載のPVC組成物。
態様5.前記組成物中の可塑剤の量がPVC樹脂100部当り可塑剤40〜120部であり、そして前記可塑剤の5〜100重量%が、テレフタル酸ジブチル、テレフタル酸ジイソブチル又はそれらの混合物である態様4に記載のPVC組成物。
態様6.ポリ塩化ビニル(PVC)樹脂とテレフタル酸ジブチル、テレフタル酸ジイソブチル及びそれらの混合物からなる群から選択された可塑剤との混合物並びに安定化量の、金属石鹸、有機亜リン酸エステル、エポキシ化合物、スズ安定剤及びそれらの混合物からなる群から選択された安定剤を含んでなるポリ塩化ビニル組成物。
態様7.(i)ポリ塩化ビニル(PVC)樹脂、(ii)PVC樹脂100部当り、テレフタル酸ジブチル、テレフタル酸ジイソブチル及びそれらの混合物からなる群から選択された可塑剤20〜800部並びに(iii)ステアリン酸バリウム/ステアリン酸亜鉛並びにエポキシ大豆油、ステアリン酸カルシウム/ステアリン酸亜鉛及びエポキシ大豆油並びにステアリン酸バリウム/ステアリン酸カドミウム及びエポキシ大豆油からなる群から選択された安定剤混合物の混合物を含んでなるポリ塩化ビニル組成物。
態様8.可塑剤がフタル酸ジオクチル、フタル酸ジ−2−エチルヘキシル、フタル酸ジイソオクチル、フタル酸ジイソノニル、フタル酸ジ−線状ノニル、ジ−線状ノニル、ウンデシルフタレート、フタル酸ジ−線状ウンデシル、フタル酸ジウンデシル、フタル酸ジイソデシル、C6−C10線状フタレート、C7線状フタレート、C9線状フタレート、C11線状フタレート、フタル酸ジトリデシル、フタル酸ウンデシルドデシル、ジ(フタル酸2−プロピルヘプチル)、フタル酸ノニルウンデシル、フタル酸テキサノールベンジル、ポリエステルフタレート、フタル酸ジアリル、n−ブチルフタリル−n−ブチルグリコセート、フタル酸ジカプリル、フタル酸ブチルシクロヘキシル、フタル酸ジシクロヘキシル、フタル酸ブチルオクチル、テレフタル酸ジオクチル、テレフタル酸ジ−2−エチルヘキシル、アジピン酸ジオクチル、アジピン酸ジ−2−エチルヘキシル、アジピン酸ジイソニル、アジピン酸ジイソオクチル、アジピン酸ジイソデシル、アジピン酸ジトリデシル、アジピン酸ジブトキシエチル、アジピン酸ジブトキシエトキシ、アジピン酸ジ(nオクチル,nデシル)、ポリエステルアジペート、ポリグリコールアジペート、トリメリト酸トリオクチル、トリメリト酸トリ−2−エチルヘキシル、トリメリト酸トリイソオクチル、トリメリト酸トリイソノニル、トリメリト酸トリイソデシル、トリメリト酸トリ−n−ヘキシル、アゼライン酸ジオクチル、グルタル酸ジ−2−エチルヘキシル、セバシン酸ジ−2−エチルヘキシル、セバシン酸ジブチル、セバシン酸ジブトキシエチル、クエン酸トリエチル、クエン酸アセチルトリエチル、クエン酸トリ−n−ブチル、クエン酸アセチルトリ−n−ブチル、クエン酸アセチルトリ−n−ヘキシル、クエン酸n−ブチルトリ−n−ヘキシル、安息香酸イソノニル、安息香酸イソデシル、1,4−シクロヘキサンジメタノールジベンゾエート、2,2,4−トリメチル−1,3−ペンタンジオールジベンゾエート、2,2−ジメチル−1,3−プロパンジオールジベンゾエート、C10−C21アルカンフェノールエステル又はアルキルスルホン酸フェノールエステル、完全硬化ひまし油との酢酸反応生成物、ペンタエリスリトールテトラベンゾエート、グリセロールトリベンゾエート、ポリプロピレングリコールジベンゾエート、トリアリールホスフェート、ジイソノニルシクロヘキサン−1,2−ジカルボキシレート、グリコールとのアジピン酸/フタレート/アジペート/セバケートのポリマー及びしばしば酸末端のもの、フタル酸ブチルベンジル、フタル酸アルキルベンジル、フタル酸C7−C9ブチル、ジエチレングリコールジベンゾエート、ジプロピレングリコールジベンゾエート、安息香酸2−エチルヘキシル、安息香酸テキサノール、エチレングリコールジベンゾエート、プロピレングリコールジベンゾエート、トリエチレングリコールジベンゾエート、フタル酸ジ−ヘプチル、フタル酸ジヘキシル、フタル酸ジメチル、フタル酸ジエチル、フタル酸ジブチル、フタル酸ジイソブチル並びにそれらの混合物からなる群から選択された追加の可塑剤を更に含み、そして該可塑剤の10〜100重量%がテレフタル酸ジブチル、テレフタル酸ジイソブチル及びそれらの混合物からなる群から選択される態様7に記載のPVC組成物。
態様9.前記可塑剤の量が、PVC樹脂100部当り可塑剤40〜120部であり、そして前記可塑剤の25〜100重量%がテレフタル酸ジブチル、テレフタル酸ジイソブチル及びそれらの混合物からなる群から選択される態様8に記載のPVC組成物。
態様10.(i)ポリ塩化ビニル(PVC)樹脂、(ii)PVC樹脂100部当り可塑剤20〜800部(ここで可塑剤はテレフタル酸ジブチル、テレフタル酸ジイソブチル及びそれらの混合物からなる群から選択される)並びに(iii)ステアリン酸バリウム/ステアリン酸亜鉛及びエポキシ大豆油、ステアリン酸カルシウム/ステアリン酸亜鉛及びエポキシ大豆油並びにステアリン酸バリウム/ステアリン酸カドミウム及びエポキシ大豆油からなる群から選択された安定剤混合物の混合物を含むポリ塩化ビニル組成物。
態様11.前記組成物中の可塑剤の量がPVC樹脂100部当り可塑剤40〜120部である態様10に記載のPVC組成物。
態様12.製造物品が接着剤、シーラント、被覆された布帛、ワイヤー被膜、ケーブル被膜、発泡体、履き物、ガスケット、インク、化粧品、医療器具、床材、壁紙、屋根用膜、チューブ、インク及びカレンダー加工フィルムからなる群から選択される態様1〜11のいずれか1項に記載の組成物を含んでなる製造物品。
Claims (11)
- ポリ塩化ビニル(PVC)樹脂粒子並びにテレフタル酸ジブチル、テレフタル酸ジイソブチル及びそれらの混合物からなる群から選ばれたテレフタル酸系可塑剤を含んでなり、前記テレフタル酸系可塑剤が組成物中に、PVC樹脂100部当り、40〜120部の量で存在する自由流動粉末組成物。
- 前記テレフタル酸系可塑剤がテレフタル酸ジブチルである請求項1に記載の組成物。
- 前記テレフタル酸系可塑剤が前記組成物中に、PVC樹脂100部当り、40〜80部の量で存在する請求項1又は2に記載の組成物。
- フタル酸ジオクチル、フタル酸ジ−2−エチルヘキシル、フタル酸ジイソオクチル、フタル酸ジイソノニル、フタル酸ジ−線状ノニル、ジ−線状ノニル、ウンデシルフタレート、フタル酸ジ−線状ウンデシル、フタル酸ジウンデシル、フタル酸ジイソデシル、C6−C10線状フタレート、C7線状フタレート、C9線状フタレート、C11線状フタレート、フタル酸ジトリデシル、フタル酸ウンデシルドデシル、ジ(フタル酸2−プロピルヘプチル)、フタル酸ノニルウンデシル、フタル酸テキサノールベンジル、ポリエステルフタレート、フタル酸ジアリル、n−ブチルフタリル−n−ブチルグリコセート、フタル酸ジカプリル、フタル酸ブチルシクロヘキシル、フタル酸ジシクロヘキシル、フタル酸ブチルオクチル、テレフタル酸ジオクチル、テレフタル酸ジ−2−エチルヘキシル、アジピン酸ジオクチル、アジピン酸ジ−2−エチルヘキシル、アジピン酸ジイソニル、アジピン酸ジイソオクチル、アジピン酸ジイソデシル、アジピン酸ジトリデシル、アジピン酸ジブトキシエチル、アジピン酸ジブトキシエトキシ、アジピン酸ジ(nオクチル,nデシル)、ポリエステルアジペート、ポリグリコールアジペート、トリメリト酸トリオクチル、トリメリト酸トリ−2−エチルヘキシル、トリメリト酸トリイソオクチル、トリメリト酸トリイソノニル、トリメリト酸トリイソデシル、トリメリト酸トリ−n−ヘキシル、アゼライン酸ジオクチル、グルタル酸ジ−2−エチルヘキシル、セバシン酸ジ−2−エチルヘキシル、セバシン酸ジブチル、セバシン酸ジブトキシエチル、クエン酸トリエチル、クエン酸アセチルトリエチル、クエン酸トリ−n−ブチル、クエン酸アセチルトリ−n−ブチル、クエン酸アセチルトリ−n−ヘキシル、クエン酸n−ブチルトリ−n−ヘキシル、安息香酸イソノニル、安息香酸イソデシル、1,4−シクロヘキサンジメタノールジベンゾエート、2,2,4−トリメチル−1,3−ペンタンジオールジベンゾエート、2,2−ジメチル−1,3−プロパンジオールジベンゾエート、C10−C21アルカンフェノールエステル又はアルキルスルホン酸フェノールエステル、完全硬化ひまし油との酢酸反応生成物、ペンタエリスリトールテトラベンゾエート、グリセロールトリベンゾエート、ポリプロピレングリコールジベンゾエート、トリアリールホスフェート、ジイソノニルシクロヘキサン−1,2−ジカルボキシレート、グリコールとのアジピン酸/フタレート/アジペート/セバケートのポリマー及びしばしば酸末端のもの、フタル酸ブチルベンジル、フタル酸アルキルベンジル、フタル酸C7−C9ブチル、ジエチレングリコールジベンゾエート、ジプロピレングリコールジベンゾエート、安息香酸2−エチルヘキシル、安息香酸テキサノール、エチレングリコールジベンゾエート、プロピレングリコールジベンゾエート、トリエチレングリコールジベンゾエート、フタル酸ジ−ヘプチル、フタル酸ジヘキシル、フタル酸ジメチル、フタル酸ジエチル、フタル酸ジブチル、フタル酸ジイソブチル並びにこれらの混合物からなる群から選択された少なくとも1種の追加の可塑剤を更に含む請求項1〜3のいずれか1項に記載の組成物。
- テレフタル酸ジ−2−エチルヘキシル、フタル酸ジイソノニル、ジイソノニルシクロヘキサン−1,2−ジカルボキシレート、テレフタル酸ジオクチル、トリメリト酸トリ−2−エチルヘキシル、ジ(フタル酸2−プロピルヘプチル)、フタル酸ジイソデシル、フタル酸ジイソウンデシル、フタル酸ジトリデシル及びトリメリト酸トリイソノニルから選ばれた少なくとも1種の追加の可塑剤を更に含む請求項1〜3のいずれか1項に記載の組成物。
- テレフタル酸ジ−2−エチルヘキシル、フタル酸ジイソノニル及びジイソノニルシクロヘキサン−1,2−ジカルボキシレートから選ばれた少なくとも1種の追加の可塑剤を更に含む請求項1〜3のいずれか1項に記載の組成物。
- 前記テレフタル酸系可塑剤及び前記追加の可塑剤の合計の少なくとも10重量%が前記テレフタル酸系可塑剤である請求項4〜6のいずれか1項に記載の組成物。
- 前記テレフタル酸系可塑剤及び前記追加の可塑剤の合計の少なくとも25重量%が前記テレフタル酸系可塑剤である請求項4〜6のいずれか1項に記載の組成物。
- 前記PVC樹脂が650〜1600の重合度を有しかつASTM D−1243で測定して0.5〜1.4のインヘレント粘度を有する請求項1〜8のいずれか1項に記載の組成物。
- 前記組成物が安定剤、帯電防止剤、防曇剤、紫外線抑制剤、酸化防止剤、光安定剤、難燃剤、顔料及びそれらの混合物から選ばれる1種又はそれ以上を更に含む請求項1〜9のいずれか1項に記載の組成物。
- 請求項1〜10のいずれか1項に記載の自由流動粉末組成物を、140℃〜150℃の2本ロールミル上で加熱して、該自由流動粉末組成物を融解させる方法。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/202,543 | 2005-08-12 | ||
US11/202,543 US8372912B2 (en) | 2005-08-12 | 2005-08-12 | Polyvinyl chloride compositions |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2013015730A Division JP5775102B2 (ja) | 2005-08-12 | 2013-01-30 | ポリ塩化ビニル組成物 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2014224275A JP2014224275A (ja) | 2014-12-04 |
JP5912157B2 true JP5912157B2 (ja) | 2016-04-27 |
Family
ID=37398894
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2008526248A Active JP5442992B2 (ja) | 2005-08-12 | 2006-08-10 | ポリ塩化ビニル組成物 |
JP2013015730A Expired - Fee Related JP5775102B2 (ja) | 2005-08-12 | 2013-01-30 | ポリ塩化ビニル組成物 |
JP2014184207A Active JP5912157B2 (ja) | 2005-08-12 | 2014-09-10 | ポリ塩化ビニル組成物 |
Family Applications Before (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2008526248A Active JP5442992B2 (ja) | 2005-08-12 | 2006-08-10 | ポリ塩化ビニル組成物 |
JP2013015730A Expired - Fee Related JP5775102B2 (ja) | 2005-08-12 | 2013-01-30 | ポリ塩化ビニル組成物 |
Country Status (7)
Country | Link |
---|---|
US (2) | US8372912B2 (ja) |
EP (1) | EP1913069A1 (ja) |
JP (3) | JP5442992B2 (ja) |
CN (1) | CN101238175B (ja) |
CA (1) | CA2617786C (ja) |
NO (1) | NO20081219L (ja) |
WO (1) | WO2007021987A1 (ja) |
Families Citing this family (133)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8372912B2 (en) | 2005-08-12 | 2013-02-12 | Eastman Chemical Company | Polyvinyl chloride compositions |
WO2007120278A1 (en) * | 2005-11-23 | 2007-10-25 | Polyone Corporation | Use of a blend of phthalate plasticizers in poly(vinyl halide) compounds |
DE102006001795A1 (de) * | 2006-01-12 | 2007-07-19 | Oxeno Olefinchemie Gmbh | Terephthalsäuredialkylester und deren Verwendung |
EP2007210A4 (en) | 2006-02-10 | 2011-07-06 | Dupont Tate & Lyle Bio Products Company Llc | COMPOSITIONS WITH MONO AND DIESELS FROM 1,3-PROPANEL ON BIOLOGICAL BASIS |
JP4798494B2 (ja) * | 2006-04-07 | 2011-10-19 | 富士電機株式会社 | 電子写真用感光体およびその製造方法 |
CA2661173C (en) * | 2006-08-30 | 2012-08-28 | Eastman Chemical Company | Sealant compositions having a novel plasticizer |
CA2661168C (en) * | 2006-08-30 | 2011-11-08 | Eastman Chemical Company | Terephthalates as plasticizers in vinyl acetate polymer compositions |
US7361779B1 (en) * | 2007-04-18 | 2008-04-22 | Eastman Chemical Company | Low-melting mixtures of di-n-butyl and diisobutyl terephthalate |
US20090288359A1 (en) * | 2007-06-07 | 2009-11-26 | Martin Jr Joel E | Polyvinyl Chloride (PVC) Compositions and Reinforced Flexible PVC Flooring With Improved Performance Formed of the Same |
KR100812511B1 (ko) | 2007-06-25 | 2008-03-11 | 주식회사 엘지화학 | 무독 및 저취 벽지용 염화비닐계 발포 수지 조성물 |
KR100812512B1 (ko) | 2007-06-25 | 2008-03-11 | 주식회사 엘지화학 | 지우개용 염화비닐계 수지 조성물 |
KR100838474B1 (ko) | 2007-06-26 | 2008-06-16 | 주식회사 엘지화학 | 투명 연질 시트용 염화비닐계 수지 조성물 |
KR100872686B1 (ko) | 2007-06-26 | 2008-12-10 | 주식회사 엘지화학 | 전선 외장 피복재용 염화비닐계 수지 조성물 |
US7741395B2 (en) * | 2007-08-21 | 2010-06-22 | Eastman Chemical Company | Low volatile organic content viscosity reducer |
US20090124737A1 (en) * | 2007-11-12 | 2009-05-14 | Eastman Chemical Company | Acrylic plastisol viscosity reducers |
US20100113664A1 (en) * | 2008-06-11 | 2010-05-06 | Ferro Corporation | Asymmetric Cyclic Diester Compounds |
US8383698B2 (en) * | 2008-09-10 | 2013-02-26 | Bridgestone Corporation | Esters of cyclohexane polycarboxylic acids as plasticizers in rubber compounds |
KR20100031391A (ko) * | 2008-09-12 | 2010-03-22 | 에스케이에너지 주식회사 | 가소제 및 이를 포함한 폴리염화비닐 수지 조성물 |
EP2182135A1 (fr) * | 2008-10-28 | 2010-05-05 | Tarkett GDL S.A. | Revêtement de surface amovible |
CN102272215A (zh) | 2008-12-18 | 2011-12-07 | 埃克森美孚化学专利公司 | 包含对苯二甲酸酯的聚合物组合物 |
JP5237156B2 (ja) * | 2009-03-10 | 2013-07-17 | リケンファブロ株式会社 | ポリ塩化ビニル系高ストレッチフィルム |
TWI381014B (zh) * | 2009-05-15 | 2013-01-01 | China Steel Corp | A rubber composition, a rubber roller obtained by using the composition, and a method for producing the same |
CN101987888B (zh) * | 2009-08-07 | 2012-05-23 | 成都亚恩科技实业有限公司 | 一种多元醇苯甲酸酯增塑剂 |
CN101987819B (zh) * | 2009-08-07 | 2012-08-22 | 成都亚恩科技实业有限公司 | 一种多元醇苯甲酸酯增塑剂的制备方法 |
WO2011113707A1 (en) * | 2010-03-17 | 2011-09-22 | Exxonmobil Chemical Patents Inc. | Plasticiser blends and compositions and articles made therefrom |
CN101962461B (zh) * | 2010-10-25 | 2015-05-06 | 欧阳伟 | 不含邻苯二甲酸酯的医用聚氯乙烯塑料 |
CN101962460A (zh) * | 2010-10-25 | 2011-02-02 | 欧阳伟 | 耐辐照不含邻苯二甲酸酯的医用聚氯乙烯塑料 |
DE102010061871A1 (de) * | 2010-11-24 | 2012-05-24 | Evonik Oxeno Gmbh | Polymer-Zusammensetzung enthaltend DINT als Weichmacher |
EP2646498A2 (en) * | 2010-12-03 | 2013-10-09 | PolyOne Corporation | Plastisol for spray-molded plastic articles |
DE102011004675A1 (de) * | 2011-02-24 | 2012-08-30 | Evonik Oxeno Gmbh | C11 bis C13 Dialkylester der Furandicarbonsäure |
JP2012184529A (ja) * | 2011-03-07 | 2012-09-27 | Okamoto Kk | 壁紙 |
CN102229730B (zh) * | 2011-06-02 | 2013-03-13 | 浙江铭龙塑胶有限公司 | 一种浴帘的制造方法 |
JP6059911B2 (ja) * | 2011-08-31 | 2017-01-11 | リケンテクノス株式会社 | 塩化ビニル樹脂組成物 |
EP3351101A1 (en) | 2011-09-19 | 2018-07-25 | Fenwal, Inc. | Container for storing red blood cells |
CN102417675A (zh) * | 2011-09-23 | 2012-04-18 | 安徽万朗磁塑集团有限公司 | 一种新型环保绿色抗菌门封条胶套的材料配方及制备方法 |
CN102604260B (zh) * | 2012-02-25 | 2014-04-02 | 安徽电缆股份有限公司 | 一种改性软聚氯乙烯护套电缆料及其制备方法 |
JP2014114359A (ja) * | 2012-12-07 | 2014-06-26 | Tosoh Corp | ポリ塩化ビニル系ペースト樹脂組成物 |
US10398625B2 (en) | 2013-03-13 | 2019-09-03 | Fenwal, Inc. | Medical containers with terephthalate plasticizer for storing red blood cell products |
CN104284917A (zh) * | 2013-05-08 | 2015-01-14 | Lg化学株式会社 | 酯组合物的制备方法和树脂组合物 |
PL2821431T3 (pl) | 2013-05-08 | 2017-02-28 | Lg Chem, Ltd. | Kompozycja na bazie estrów, sposób jej wytwarzania i kompozycja żywicy zawierająca kompozycję estrową |
US9587087B2 (en) | 2013-05-08 | 2017-03-07 | Lg Chem, Ltd. | Method for preparing ester composition and resin composition |
CN103289247A (zh) * | 2013-06-24 | 2013-09-11 | 苏州新区佳合塑胶有限公司 | 绝缘电工套管用塑料及其制备方法 |
CN103694598A (zh) * | 2013-12-10 | 2014-04-02 | 江苏三角洲塑化有限公司 | 一种耐聚苯乙烯迁移阻燃pvc护层料及其制备方法 |
CN104448603A (zh) * | 2013-12-19 | 2015-03-25 | 惠州乐庭电子线缆有限公司 | 一种透明阻燃交联聚氯乙烯电线电缆料及其制备方法 |
CN105874005A (zh) | 2014-01-03 | 2016-08-17 | 塔吉特Gdl公司 | 改进的无邻苯二甲酸酯的聚氯乙烯增塑溶胶组合物 |
KR20160125389A (ko) | 2014-02-20 | 2016-10-31 | 프레제니우스 헤모케어 네덜란드 비.브이. | 적혈구 제품, 혈장 및 혈소판의 보관을 위한 비-dehp 가소제를 갖는 의료용 컨테이너 및 시스템 구성요소 |
JP6506955B2 (ja) * | 2014-03-11 | 2019-04-24 | 日東電工株式会社 | 粘着テープ |
CN104045936B (zh) * | 2014-06-19 | 2016-06-08 | 成都鑫成鹏高分子科技股份有限公司 | 用于耐超低温电线电缆的组合物及其加工方法 |
US20150367563A1 (en) * | 2014-06-23 | 2015-12-24 | Shoreline Plastics, LLC | Substrate with protective polyvinyl chloride sleeve |
TW201609628A (zh) * | 2014-07-08 | 2016-03-16 | 巴斯夫歐洲公司 | 包含脂族二羧酸二酯及對苯二甲酸二烷基酯之塑化劑組成物 |
CN104153241B (zh) * | 2014-07-15 | 2017-01-11 | 安徽紫荆花壁纸股份有限公司 | Pvc发泡壁纸用高硬高韧耐刮擦pvc糊料及其制备方法 |
JP6435483B2 (ja) * | 2014-07-31 | 2018-12-12 | 平岡織染株式会社 | 接着性ペーストゾル組成物及びそれを用いた産業資材用帆布及びメッシュシートの製造方法 |
US20160075857A1 (en) * | 2014-09-16 | 2016-03-17 | Eastman Chemical Company | Polymeric compositions with improved noise suppression |
US9809010B2 (en) | 2014-10-15 | 2017-11-07 | Solutia Inc. | Multilayer interlayer having sound damping properties over a broad temperature range |
EP3210642A4 (en) * | 2014-10-22 | 2018-06-13 | Shenzhen Yuantai Medical Equipment Co., Ltd. | Breathing bag |
EP3018166A1 (en) * | 2014-11-05 | 2016-05-11 | Clariant International Ltd. | Concentrate composition for polymeric chain extension |
US9925746B2 (en) | 2014-12-08 | 2018-03-27 | Solutia Inc. | Poly(vinyl acetal) resin compositions, layers, and interlayers having enhanced optical properties |
US9975315B2 (en) | 2014-12-08 | 2018-05-22 | Solutia Inc. | Poly(vinyl acetal) resin compositions, layers, and interlayers having enhanced optical properties |
CN107207817B (zh) * | 2014-12-08 | 2021-01-05 | 首诺公司 | 具有增强的光学特性的聚(乙烯醇缩醛)树脂组合物、层和夹层 |
US9963583B2 (en) | 2014-12-08 | 2018-05-08 | Solutia Inc. | Poly(vinyl acetal) resin compositions, layers, and interlayers having enhanced optical properties |
US20160159051A1 (en) | 2014-12-08 | 2016-06-09 | Solutia Inc. | Poly(vinyl acetal) resin compositions, layers, and interlayers having enhanced optical properties |
US9587086B2 (en) * | 2014-12-08 | 2017-03-07 | Eastman Chemical Company | Poly(vinyl acetal) resin compositions, layers, and interlayers having enhanced optical properties |
KR101799588B1 (ko) | 2015-01-15 | 2017-11-21 | 한남대학교 산학협력단 | 사출이 용이한 연성 친환경 조성물 |
EP3250635B1 (de) * | 2015-01-30 | 2018-10-24 | Basf Se | Weichmacher-zusammensetzung, die polymere dicarbonsäureester und terephthalsäuredialkylester enthält |
KR101845338B1 (ko) * | 2015-02-04 | 2018-04-04 | 한화케미칼 주식회사 | 친환경 가소제 조성물, 및 이를 포함하는 염화비닐 수지 조성물 |
KR101674317B1 (ko) * | 2015-02-12 | 2016-11-08 | 주식회사 엘지화학 | 가소제 조성물, 수지 조성물 및 이들의 제조 방법 |
WO2016129876A1 (ko) * | 2015-02-12 | 2016-08-18 | 주식회사 엘지화학 | 가소제 조성물, 수지 조성물 및 이들의 제조 방법 |
CN104667354A (zh) * | 2015-03-10 | 2015-06-03 | 丁莉 | 一种神经介入血管造影用导管 |
KR101777143B1 (ko) | 2015-03-19 | 2017-09-18 | 애경유화주식회사 | 복합 가소제 조성물 및 이를 이용한 고분자 수지 조성물 |
KR101901010B1 (ko) | 2015-03-20 | 2018-09-20 | 주식회사 엘지화학 | 가소제 조성물, 수지 조성물 및 이들의 제조 방법 |
WO2016153235A1 (ko) * | 2015-03-20 | 2016-09-29 | 주식회사 엘지화학 | 가소제 조성물, 수지 조성물 및 이들의 제조 방법 |
WO2016153236A1 (ko) * | 2015-03-20 | 2016-09-29 | 주식회사 엘지화학 | 가소제 조성물, 수지 조성물 및 이들의 제조 방법 |
KR101846066B1 (ko) * | 2015-04-06 | 2018-04-06 | 주식회사 엘지화학 | 가소제 조성물을 포함하는 수지 조성물 및 이들의 제조 방법 |
CN104945766A (zh) * | 2015-05-19 | 2015-09-30 | 苏州德翔装饰工程有限公司 | 一种厨房顶板用复合高分子材料及其制备方法 |
JP6145198B2 (ja) * | 2015-06-19 | 2017-06-07 | 積水化学工業株式会社 | 耐火樹脂成形体およびそれを備えた建具 |
EP3112409A1 (en) * | 2015-06-30 | 2017-01-04 | Scg Chemicals Co. Ltd. | Plasticizer composition |
JP6503946B2 (ja) * | 2015-07-13 | 2019-04-24 | 日立金属株式会社 | 塩化ビニル樹脂組成物並びにこれを用いた電線及びケーブル |
JP6512003B2 (ja) * | 2015-07-13 | 2019-05-15 | 日立金属株式会社 | 電線・ケーブル用塩化ビニル樹脂組成物並びにこれを用いた電線及びケーブル |
JP6503947B2 (ja) | 2015-07-13 | 2019-04-24 | 日立金属株式会社 | 塩化ビニル樹脂組成物並びにこれを用いた電線及びケーブル |
KR101793383B1 (ko) | 2015-07-24 | 2017-11-20 | 주식회사 엘지화학 | 가소제 조성물, 수지 조성물 및 이들의 제조 방법 |
WO2017018740A1 (ko) * | 2015-07-24 | 2017-02-02 | 주식회사 엘지화학 | 가소제 조성물, 수지 조성물 및 이들의 제조 방법 |
CN107429026A (zh) * | 2015-07-28 | 2017-12-01 | Lg化学株式会社 | 增塑剂组合物,树脂组合物及其制备方法 |
JP6525316B2 (ja) | 2015-07-29 | 2019-06-05 | 東リ株式会社 | 床材 |
CN105086236B (zh) * | 2015-08-14 | 2017-07-11 | 联塑科技发展(贵阳)有限公司 | 一种硬质聚氯乙烯(u‑pvc)塑料及其管件和制作方法 |
US20180291180A1 (en) * | 2015-09-30 | 2018-10-11 | Basf Se | Plasticizer composition containing polymeric dicarboxylic acid esters and dicarboxylic acid diesters |
RU2743641C1 (ru) * | 2015-09-30 | 2021-02-20 | Басф Се | Пластифицирующая композиция, содержащая полимерные сложные эфиры дикарбоновых кислот и сложные диалкиловые эфиры терефталевой кислоты |
CN107531938A (zh) | 2015-10-27 | 2018-01-02 | 株式会社Lg化学 | 增塑剂组合物、树脂组合物及其制备方法 |
EP3369771B1 (en) | 2015-10-27 | 2021-06-09 | LG Chem, Ltd. | Plasticizer composition, resin composition, and methods for preparing same |
US10590260B2 (en) | 2015-10-27 | 2020-03-17 | Lg Chem, Ltd. | Plasticizer composition, resin composition, and methods for preparing same |
CN105367821A (zh) * | 2015-11-13 | 2016-03-02 | 宣城市聚源精细化工有限公司 | 一种新型增塑剂 |
CN105367822A (zh) * | 2015-11-13 | 2016-03-02 | 宣城市聚源精细化工有限公司 | 一种增塑剂 |
CN114316475A (zh) * | 2015-11-27 | 2022-04-12 | 株式会社Lg化学 | 增塑剂组合物、树脂组合物及其制备方法 |
RU2633963C2 (ru) * | 2015-12-29 | 2017-10-20 | Публичное акционерное общество "СИБУР Холдинг" | Композиция пластификатора для поливинилхлорида, пластизоль и пластификат на ее основе |
JP6649581B2 (ja) * | 2016-02-02 | 2020-02-19 | 新日本理化株式会社 | 低粘度の可塑剤を配合した塩化ビニル系ペーストゾル組成物 |
KR102594220B1 (ko) * | 2016-02-29 | 2023-10-25 | 린텍 가부시키가이샤 | 반도체 가공 시트 |
WO2017150017A1 (ja) * | 2016-02-29 | 2017-09-08 | リンテック株式会社 | 半導体加工シート用基材フィルムおよび半導体加工シート |
KR102090294B1 (ko) | 2016-04-22 | 2020-03-17 | 주식회사 엘지화학 | 가소제 조성물 및 이를 포함하는 수지 조성물 |
WO2017183876A1 (ko) * | 2016-04-22 | 2017-10-26 | 주식회사 엘지화학 | 가소제 조성물 및 이를 포함하는 수지 조성물 |
EP3241866A1 (en) | 2016-05-04 | 2017-11-08 | Clariant Plastics & Coatings Ltd | Composition for polyester hydrolytic stabilization |
MX2018014011A (es) | 2016-05-17 | 2019-02-26 | Gen Cable Technologies Corp | Composiciones retardantes de incendios y separadores de cables formados de las mismas. |
KR101994251B1 (ko) * | 2016-05-18 | 2019-06-28 | 주식회사 엘지화학 | 가소제 조성물 및 이를 포함하는 수지 조성물 |
EP3327076B1 (en) * | 2016-05-18 | 2022-06-29 | LG Chem, Ltd. | Plasticizer composition and resin composition comprising same |
WO2017210436A1 (en) * | 2016-06-01 | 2017-12-07 | Kang Hack S | Ultra low thermo fusion pvc alternative plastisol coating and textile printing ink |
WO2017210431A1 (en) * | 2016-06-01 | 2017-12-07 | Kang Hack S | Ultra low thermo fusion pvc plastisol coating and textile printing ink |
EP3481589B1 (en) * | 2016-07-08 | 2023-08-30 | Saint-Gobain Abrasives, Inc. | Abrasive articles |
CN106118171A (zh) * | 2016-07-19 | 2016-11-16 | 董芬芳 | 一种金属用重防腐蚀防锈漆 |
US20190161598A1 (en) * | 2016-08-01 | 2019-05-30 | Basf Se | Plasticizer composition |
KR101806943B1 (ko) | 2016-09-07 | 2017-12-08 | 애경유화 주식회사 | 유연성 pvc 수지 조성물 |
WO2018075663A1 (en) * | 2016-10-18 | 2018-04-26 | Interface Biologics, Inc. | Plasticized pvc admixtures with surface modifying macromolecules and articles made therefrom |
CN110678524A (zh) | 2017-03-01 | 2020-01-10 | 巴斯夫欧洲公司 | 包含pvc和增塑组分的涂覆剂组合物 |
KR102187174B1 (ko) | 2017-05-25 | 2020-12-07 | 주식회사 엘지화학 | 시트레이트계 가소제 및 이를 포함하는 수지 조성물 |
BR112020005352B1 (pt) | 2017-10-13 | 2023-11-07 | Lg Chem, Ltd | Composição de plasticizador e composição de resina incluindo a mesma |
EP3473669B1 (en) * | 2017-10-20 | 2020-12-02 | Eastman Chemical Company | Method of controlling plastisol viscosity |
CN107722614B (zh) * | 2017-10-26 | 2020-07-17 | 湖北雄志塑胶五金制品有限公司 | 一种复合树脂材料及其制备方法 |
KR102236923B1 (ko) * | 2017-12-04 | 2021-04-07 | 주식회사 엘지화학 | 가소제 조성물 및 이를 포함하는 수지 조성물 |
CN108501133A (zh) * | 2017-12-30 | 2018-09-07 | 张梦琪 | 一种pvc贴面胶合板及其制造方法 |
RU2681631C1 (ru) * | 2018-03-29 | 2019-03-11 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Уфимский государственный нефтяной технический университет" | Пластификатор поливинилхлорида |
CN109134926A (zh) * | 2018-06-25 | 2019-01-04 | 西安医学院 | 一种用于聚氯乙烯树脂的复配型环保增塑剂及其制备方法 |
EP3814406A4 (en) * | 2018-06-28 | 2022-03-16 | Emerald Kalama Chemical, LLC | LUXURY VINYL TILE MODIFIERS TO INCREASE HARDNESS AND STIFFNESS |
JP7541221B2 (ja) * | 2018-08-10 | 2024-08-28 | 裕 山田 | 可塑剤組成物及び物品塗布用可塑剤組成物 |
CN109457494B (zh) * | 2018-11-07 | 2021-08-03 | 英德市宏利皮革有限公司 | 一种耐清洗剂的聚氯乙烯人造革 |
US20220010093A1 (en) * | 2018-11-28 | 2022-01-13 | Oxy Usa Inc. | Plasticized polyvinyl chloride compositions with enhanced resistance to biological growth |
WO2020152637A1 (en) * | 2019-01-25 | 2020-07-30 | Reliance Industries Limited | Internally plasticized polyvinyl chloride and a process for preparation thereof |
CN114080419B (zh) * | 2019-06-26 | 2024-03-29 | 伊士曼化工公司 | 高溶剂化混合对苯二甲酸酯增塑剂组合物 |
US20220325069A1 (en) * | 2019-06-26 | 2022-10-13 | Eastman Chemical Company | Novel non-phthalate plasticizer blends for poly(vinyl chloride) resin compositions |
CN110551429B (zh) * | 2019-10-23 | 2021-08-10 | 广东时利和汽车实业集团有限公司 | 一种提高酸酐-环氧体系耐高湿涂装胶附着力的方法 |
DE102020002686A1 (de) * | 2020-05-05 | 2021-11-11 | Staedtler Mars Gmbh & Co. Kg | Modelliermasse sowie Verfahren zu deren Herstellung |
KR102506279B1 (ko) * | 2020-07-01 | 2023-03-03 | 한화솔루션 주식회사 | 가소제 조성물, 및 이를 포함하는 염화비닐 수지 조성물 |
CN115698155B (zh) * | 2020-08-10 | 2024-03-29 | 株式会社Lg化学 | 乙酰柠檬酸酯类增塑剂组合物和包含其的树脂组合物 |
JP7515957B2 (ja) * | 2021-01-29 | 2024-07-16 | エルジー・ケム・リミテッド | 可塑剤組成物およびこれを含む樹脂組成物 |
CN113072784A (zh) * | 2021-03-22 | 2021-07-06 | 台州联成新材料有限公司 | 一种耐油电缆料及其制备方法 |
CN114378973B (zh) * | 2021-12-30 | 2024-06-28 | 台州市手护神科技有限公司 | 一种改性pvc复合手套及其制备方法 |
CN115232005B (zh) * | 2022-07-01 | 2024-05-10 | 绍兴宏润消防器材有限公司 | 一种酯交换增塑剂及制备方法 |
Family Cites Families (160)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2217163A (en) * | 1939-03-07 | 1940-10-08 | Du Pont | Plastic composition |
US2360306A (en) * | 1939-06-29 | 1944-10-10 | Monsanto Chemicals | Plastic polyvinyl acetal compositions |
US2459955A (en) * | 1945-10-17 | 1949-01-25 | Shawinigan Chem Ltd | Polyvinyl acetate emulsion adhesive |
US2628207A (en) * | 1949-09-14 | 1953-02-10 | Standard Oil Dev Co | Terephthalate esters as plasticizers for polyvinyl resins |
NL109801C (ja) | 1954-09-09 | |||
GB851753A (en) | 1956-11-23 | 1960-10-19 | Union Carbide Corp | Vinyl chloride resin compositions |
US3224995A (en) | 1961-02-16 | 1965-12-21 | Ethyl Corp | Polyvinyl chloride plasticized with dialkoxyalkyl homoterephthalates |
US3431239A (en) * | 1965-03-29 | 1969-03-04 | Prod Res & Chem Corp | Mercaptan terminated polyethers |
US3764374A (en) | 1970-07-21 | 1973-10-09 | Eastman Kodak Co | Process for placing modifiers within polyester fibers and films |
US3725311A (en) | 1972-05-15 | 1973-04-03 | Thuron Industries | Low temperature extrudable odor-neutralizing composition |
US3929867A (en) | 1973-08-06 | 1975-12-30 | Eastman Kodak Co | Mixed ester plastic additive |
US4082712A (en) * | 1975-03-03 | 1978-04-04 | Hooker Chemicals & Plastics Corporation | Process for curing sulfhydryl-terminated thioether polymers |
US4015044A (en) * | 1975-03-27 | 1977-03-29 | Union Carbide Corporation | Process of bonding polyurethane-sealants and caulks |
US4110261A (en) * | 1975-09-18 | 1978-08-29 | W & F Mfg. Co., Inc. | Fragrance-emitting article having a polymer-petroleum wax composition |
JPS5521446Y2 (ja) | 1976-11-01 | 1980-05-23 | ||
JPS53117035A (en) | 1977-03-23 | 1978-10-13 | Kuraray Co Ltd | Pressure-sensitive |
US4221688A (en) * | 1978-04-28 | 1980-09-09 | Dow Corning Corporation | Silicone emulsion which provides an elastomeric product and methods for preparation |
JPS6040470B2 (ja) * | 1978-08-02 | 1985-09-11 | 三菱化成ポリテック株式会社 | 塩化ビニル樹脂組成物 |
US4331579A (en) * | 1979-10-04 | 1982-05-25 | Congoleum Corporation | Adhesive to adhere impervious and felt backed vinyl sheet material to damp concrete |
US4253898A (en) | 1979-12-17 | 1981-03-03 | The B. F. Goodrich Company | Bonding composition and microwave process for bonding together plastic components |
US4362783A (en) | 1980-08-26 | 1982-12-07 | Western Electric Company, Incorporated | Polymer coatings and methods of applying same |
US4366307A (en) | 1980-12-04 | 1982-12-28 | Products Research & Chemical Corp. | Liquid polythioethers |
US4376144A (en) | 1981-04-08 | 1983-03-08 | Monsanto Company | Treated fibers and bonded composites of cellulose fibers in vinyl chloride polymer characterized by an isocyanate bonding agent |
US4414267A (en) | 1981-04-08 | 1983-11-08 | Monsanto Company | Method for treating discontinuous cellulose fibers characterized by specific polymer to plasticizer and polymer-plasticizer to fiber ratios, fibers thus treated and composites made from the treated fibers |
US4401720A (en) | 1981-06-24 | 1983-08-30 | Eastman Kodak Company | Poly(vinyl chloride) plastisol compositions |
JPS58141225A (ja) * | 1982-02-16 | 1983-08-22 | Takasago Corp | 芳香材用樹脂組成物 |
US4605465A (en) | 1982-04-26 | 1986-08-12 | W. R. Grace & Co. | UV and thermally curable, thermoplastic-containing compositions |
JPS60203658A (ja) * | 1984-03-28 | 1985-10-15 | Toyoda Gosei Co Ltd | ポリ塩化ビニル樹脂組成物 |
US4654390A (en) | 1984-08-10 | 1987-03-31 | The Dow Chemical Company | Monomeric plasticizers for halogen-containing resins |
JPS6155104A (ja) | 1984-08-24 | 1986-03-19 | Toho Titanium Co Ltd | オレフィン類重合用触媒成分 |
US4666765A (en) * | 1985-10-02 | 1987-05-19 | Caldwell James M | Silicone coated fabric |
US4764449A (en) | 1985-11-01 | 1988-08-16 | The Chromaline Corporation | Adherent sandblast photoresist laminate |
DE3783078D1 (de) * | 1986-05-27 | 1993-01-28 | Ici Plc | Dichtungszusammensetzung auf wasserbasis. |
JPS6375050A (ja) * | 1986-09-19 | 1988-04-05 | Mitsubishi Kasei Vinyl Co | 塩化ビニル系樹脂組成物 |
JPS6375050U (ja) | 1986-11-06 | 1988-05-19 | ||
GB8707890D0 (en) | 1987-04-02 | 1987-05-07 | Bp Chem Int Ltd | Polymer composition |
US4792464A (en) | 1987-06-01 | 1988-12-20 | Martenson Irvin W | Corrosion coating composition |
JPS6445452A (en) | 1987-08-12 | 1989-02-17 | Plus Teku Kk | Thermoplastic polymer composition |
US5179138A (en) * | 1988-01-25 | 1993-01-12 | Chisso Corporation | Process for producing a vinyl chloride resin composition for powder molding |
US4900771A (en) | 1989-01-26 | 1990-02-13 | Aster, Inc. | Hot applied plastisol compositions |
US5071690A (en) | 1989-02-01 | 1991-12-10 | Diafoil Company, Limited | Moldable biaxially stretched polyester film |
CA2015736A1 (en) | 1989-05-11 | 1990-11-11 | Diane G. Schmidt | Perfume particles for use in cleaning and conditioning compositions |
US5236883A (en) * | 1989-12-05 | 1993-08-17 | Oji Paper Co., Ltd. | Heat-sensitive recording material |
YU77891A (sh) | 1990-05-03 | 1994-05-10 | Lcv International Limited | Štamparska boja i postupak štampanja |
JPH04132755A (ja) * | 1990-09-25 | 1992-05-07 | Sumitomo Chem Co Ltd | 粉末成形用塩化ビニル系樹脂組成物 |
WO1992018601A1 (en) | 1991-04-16 | 1992-10-29 | Minnesota Mining And Manufacturing Company | Improvements in coated perfume particles |
CA2041532C (en) * | 1991-04-30 | 2002-01-01 | Hamdy Khalil | Urethane sealant having improved sag properties |
JP2999577B2 (ja) * | 1991-06-07 | 2000-01-17 | サンスター技研株式会社 | ポリ塩化ビニルプラスチゾル系シーラー組成物 |
US5458953A (en) * | 1991-09-12 | 1995-10-17 | Mannington Mills, Inc. | Resilient floor covering and method of making same |
AU2877792A (en) * | 1991-10-22 | 1993-05-21 | Dap Products Inc. | Moisture curable silicone-urethane copolymer sealants |
US5367734A (en) * | 1991-11-04 | 1994-11-29 | Terry; Raymond | Pliable abrasive pellet for abrading fabrics |
US5698621A (en) * | 1992-03-06 | 1997-12-16 | Achilles Usa, Inc. | Printable self-clinging polyvinyl chloride film and methods relating thereto |
JPH05262942A (ja) * | 1992-03-19 | 1993-10-12 | Asahi Denka Kogyo Kk | 塩素含有樹脂組成物 |
US5401708A (en) * | 1992-05-19 | 1995-03-28 | Kanzaki Paper Mfg. Co., Ltd. | Heat-sensitive recording material |
US6323275B2 (en) * | 1992-05-28 | 2001-11-27 | Toagosei Co., Ltd. | Cyanoacrylate adhesive composition |
US5454801A (en) * | 1992-10-09 | 1995-10-03 | Mcneil-Ppc, Inc. | Printed polymer coatings and method for making same |
DE4235151A1 (de) * | 1992-10-19 | 1994-04-21 | Hoechst Ag | Polyvinylacetale, die emulgatorfreie wäßrige Dispersionen und redispergierbare trockene Pulver bilden können, Verfahren zu ihrer Herstellung und ihre Verwendung |
JPH06258772A (ja) | 1993-03-08 | 1994-09-16 | Fuji Photo Film Co Ltd | ロールフィルムの接合方法及び接合解除方法 |
US5366550A (en) * | 1993-04-02 | 1994-11-22 | Tec Incorporated | Latex modified cement-based thin set adhesive |
DE4415888A1 (de) | 1993-05-14 | 1994-11-17 | Basf Ag | Schnell abbindende, zweikomponentige Dichtungs- oder Spachtelmassen |
USRE36233E (en) * | 1993-08-03 | 1999-06-22 | Osi Specialties, Inc. | Use of softening additives in polyurethane foam |
ZA945718B (en) * | 1993-08-03 | 1995-03-09 | Osi Specialties Inc | Process for forming polyurethane foam using mechanical cooling and an additive |
US5489618A (en) * | 1993-11-29 | 1996-02-06 | Osi Specialties, Inc. | Process for preparing polyurethane foam |
NZ278776A (en) * | 1994-01-07 | 1998-01-26 | Minnesota Mining & Mfg | Graphics transfer article with overlayer comprising a premask layer which, in turn, comprises a protective layer which protects an image that has been applied to a target substrate |
JPH07286153A (ja) | 1994-04-20 | 1995-10-31 | Sekisui Chem Co Ltd | 接着剤組成物及び該接着剤組成物を用いた紙管 |
AU672159B2 (en) * | 1994-06-14 | 1996-09-19 | National Starch And Chemical Investment Holding Corporation | High performance PVOH stabilised EVA adhesives |
JP3465355B2 (ja) | 1994-07-11 | 2003-11-10 | 大日本インキ化学工業株式会社 | 熱可塑性樹脂組成物、粘着剤および粘着基材 |
US5492960A (en) * | 1994-10-28 | 1996-02-20 | Eastman Kodak Company | Method of making polymeric particles |
GB9424246D0 (en) * | 1994-12-01 | 1995-01-18 | Dow Corning Sa | Moisture curable compositions |
JP3496992B2 (ja) * | 1994-12-08 | 2004-02-16 | 株式会社ユポ・コーポレーション | 一軸延伸多層フィルム及びそれを用いた航空タッグ |
TW424105B (en) * | 1994-12-09 | 2001-03-01 | Witco Vinyl Additives Gmbh | Stabilized polvvinvl chloride |
US5476889A (en) | 1995-01-05 | 1995-12-19 | Minnesota Mining And Manufacturing Company | Curable sealer and/or adhesive composition, and a method for coating same in a dry state with automotive paint, and coated substrates formed therewith |
US5534609A (en) * | 1995-02-03 | 1996-07-09 | Osi Specialties, Inc. | Polysiloxane compositions |
US5519072A (en) * | 1995-02-15 | 1996-05-21 | National Starch And Chemical Investment Holding Corporation | Aqueous adhesive compositions for use in binding books |
EP0773259A4 (en) * | 1995-05-25 | 1998-09-02 | Asahi Glass Co Ltd | VINYL CHLORIDE RESIN COMPOSITIONS |
JP4210328B2 (ja) * | 1995-06-07 | 2009-01-14 | ナイキ,インコーポレイテッド | ポリエステルポリオールを含有するポリウレタンをベースとした物質からなる膜 |
US5523344A (en) | 1995-06-07 | 1996-06-04 | H. B. Fuller Licensing & Financing, Inc. | Water-based adhesive formulation having enhanced characteristics |
US5900464A (en) * | 1995-07-25 | 1999-05-04 | Fmc Corporation | Processes for making methacrylate and acrylate polymers |
US5750278A (en) * | 1995-08-10 | 1998-05-12 | Westinghouse Electric Corporation | Self-cooling mono-container fuel cell generators and power plants using an array of such generators |
US6245437B1 (en) * | 1996-07-19 | 2001-06-12 | Kureha Kagaku Kogyo K.K. | Gas-barrier composite film |
US5856369A (en) * | 1996-07-30 | 1999-01-05 | Osi Specialties, Inc. | Polyethers and polysiloxane copolymers manufactured with double metal cyanide catalysts |
GB2315754A (en) * | 1996-07-30 | 1998-02-11 | Courtaulds Coatings | Curable acrylic polymer compositions and their preparation |
US5869589A (en) * | 1997-07-17 | 1999-02-09 | Raynolds; Peter Webb | Self-crosslinking aqueous dispersions |
EP0927204B1 (en) * | 1996-09-18 | 2002-11-20 | Eastman Chemical Company | Self-crosslinking aqueous dispersions |
US6284077B1 (en) * | 1997-08-29 | 2001-09-04 | Dap Products Inc. | Stable, foamed caulk and sealant compounds and methods of use thereof |
ATE258561T1 (de) * | 1997-01-28 | 2004-02-15 | Stepan Co | Emulsionspolymerisationsverfahren unter verwendung von ethylenisch ungesättigten aminsalzen von sulfonsäure,phosphorsäure und carbonsäure |
US6136884A (en) * | 1997-02-04 | 2000-10-24 | Eastman Chemical Company | Hair care compositions |
US6858260B2 (en) * | 1997-05-21 | 2005-02-22 | Denovus Llc | Curable sealant composition |
US6187125B1 (en) * | 1997-09-05 | 2001-02-13 | Arnco | Method for producing a deflation-proof pneumatic tire and tire filling composition having high resilience |
US6749836B1 (en) * | 1998-01-30 | 2004-06-15 | Eastman Chemical Company | Hair care compositions |
US6638992B1 (en) * | 1998-01-30 | 2003-10-28 | Eastman Chemical Company | Hair care compositions |
US6291536B1 (en) * | 1998-02-07 | 2001-09-18 | Dap Products Inc. | Foamed caulk and sealant compounds |
CA2321784A1 (en) * | 1998-02-27 | 1999-09-02 | Kaneka Corporation | Polymer and curable composition |
US6979716B1 (en) | 1998-06-19 | 2005-12-27 | Kaneka Corporation | Process for producing branched polymer and polymer |
CA2342788C (en) * | 1998-08-20 | 2008-10-14 | Kaneka Corporation | Resin composition, polymer and process for producing polymer |
US6127026A (en) * | 1998-09-11 | 2000-10-03 | Nike, Inc. | Flexible membranes |
HUP0103729A2 (hu) * | 1998-09-11 | 2002-01-28 | Nike International, Ltd. | Elasztomer szigetelőmembrán, valamint ilyet tartalmazó kipárnázó szerkezeti elem és lábbeli |
CA2344037A1 (en) * | 1998-09-14 | 2000-03-23 | Kaneka Corporation | Curable compositions |
JP3014094B1 (ja) * | 1998-09-28 | 2000-02-28 | 三洋化成工業株式会社 | ポリウレタン樹脂系スラッシュ成形用材料 |
US6958149B2 (en) * | 1998-10-06 | 2005-10-25 | Stryker Corporation | Repair of larynx, trachea, and other fibrocartilaginous tissues |
DE69925644T2 (de) * | 1998-10-08 | 2006-04-27 | Kaneka Corp. | Polymere und vernetzbare zusammensetzungen |
US6034168A (en) * | 1998-10-23 | 2000-03-07 | Ato Findley, Inc. | Hot melt adhesive having controllable water solubility |
DE19855599A1 (de) | 1998-12-02 | 2000-06-08 | Basf Ag | Formmassen auf Basis von Poly-C¶2¶-¶6¶-alkylenterephthalaten |
DE60037357T2 (de) * | 1999-03-18 | 2008-12-04 | Kaneka Corp. | Härtbare Zusammensetzung |
US6231849B1 (en) * | 1999-03-25 | 2001-05-15 | George A. Schiller | Simulated seminal fluid |
JP3921324B2 (ja) * | 1999-04-01 | 2007-05-30 | 三洋化成工業株式会社 | ポリウレタンペースト組成物及びシーリング材 |
US6303184B1 (en) * | 1999-05-14 | 2001-10-16 | Eastman Kodak Company | Method of forming a discontinuous polymer overcoat for imaging elements |
US6414077B1 (en) * | 1999-07-29 | 2002-07-02 | Schnee-Morehead, Inc. | Moisture curable acrylic sealants |
CA2397779A1 (en) * | 2000-01-28 | 2001-08-02 | Kaneka Corporation | Curable composition |
US7208464B2 (en) * | 2000-06-02 | 2007-04-24 | The Procter & Gamble Company | Fragrance compositions |
DE10015981A1 (de) * | 2000-03-30 | 2001-10-11 | Beiersdorf Ag | Herstellung von Acrylat-Schmelzhaftklebern aus wässrigen dispersen Systemen |
US6656998B1 (en) | 2000-05-01 | 2003-12-02 | Air Products Polymers, L.P. | Glossy paints containing emulsion polymers of vinyl acetate |
WO2001088009A1 (fr) * | 2000-05-16 | 2001-11-22 | Sunstar Giken Kabushiki Kaisha | Composition thermodurcissable |
WO2001090248A2 (en) * | 2000-05-19 | 2001-11-29 | Henkel Loctite Corporation | Impregnation sealants utilizing hydrosilation chemistry |
US20020042475A1 (en) | 2000-07-18 | 2002-04-11 | Patil Abhimanyu Onkar | Novel polyvinyl chloride resins |
US6977277B2 (en) | 2000-07-18 | 2005-12-20 | Exxonmobil Research And Engineering Company | Polyvinyl chloride resins |
US6706399B1 (en) * | 2000-08-29 | 2004-03-16 | Eastman Chemical Company | Non-blocking polymeric articles |
US6670419B2 (en) | 2000-09-14 | 2003-12-30 | Rohm And Haas Company | Method of toughening thermoplastic polymers and thermoplastic compositions produced thereby |
US6762239B1 (en) * | 2000-11-21 | 2004-07-13 | National Starch And Chemical Investment Holding Corporation | Highly functionalized ethylene-vinyl acetate emulsion copolymers |
FR2819816B1 (fr) * | 2001-01-19 | 2003-04-11 | Solvay | Compositions de polymeres comprenant des telomeres qui ont un degre de telomerisation moyen en nombre inferieur ou egal a 8 et articles ou parties d'articles fabriques en utilisant ces compositions |
JP2002234983A (ja) * | 2001-02-08 | 2002-08-23 | C I Kasei Co Ltd | 農業用ポリ塩化ビニル系樹脂フィルム |
JP2002256154A (ja) * | 2001-03-02 | 2002-09-11 | Shinto Fine Co Ltd | 良好な造膜性を持つエマルション樹脂組成物 |
US6846929B2 (en) * | 2001-04-02 | 2005-01-25 | Ciba Specialty Chemicals Corporation | Benzotriazole/hals molecular combinations and compositions stabilized therewith |
US6749861B2 (en) * | 2001-06-29 | 2004-06-15 | Lenco Laboratories, Llc | Fragrance-containing insect repellant compositions |
US6675560B2 (en) * | 2001-06-29 | 2004-01-13 | Eastman Chemical Company | PVC food wrap formed from dioctyl terphthalate plasticizer, method of forming same and method of wrapping food therewith |
DK1408961T3 (da) * | 2001-07-16 | 2007-11-05 | Hoffmann La Roche | 2 pyrrolidon-derivater som prostanoide agonister |
JP3966277B2 (ja) * | 2001-08-10 | 2007-08-29 | Nok株式会社 | 加硫ゴム−樹脂複合体の製造法 |
US7012148B2 (en) * | 2001-09-25 | 2006-03-14 | Trustees Of Dartmouth College | Compositions and methods for thionation during chemical synthesis reactions |
WO2003029339A1 (en) * | 2001-09-25 | 2003-04-10 | Exxonmobil Chemical Patents Inc. | Plasticised polyvinyl chloride |
US6855765B2 (en) * | 2001-12-12 | 2005-02-15 | National University Of Singapore | Heat and hot water resistant polyurethane sealant |
US6849675B2 (en) | 2002-01-23 | 2005-02-01 | Acushnet Company | Golf ball comprising a plasticized polyurethane |
JP2003301082A (ja) * | 2002-04-09 | 2003-10-21 | Mitsubishi Chemicals Corp | 塩化ビニル系樹脂組成物 |
US7517923B2 (en) | 2002-05-07 | 2009-04-14 | National Institute Of Advanced Industrial Science And Technology | Raw material composition |
US6887964B2 (en) * | 2002-05-31 | 2005-05-03 | Bayer Materialscience Llc | Moisture-curable, polyether urethanes with reactive silane groups and their use as sealants, adhesives and coatings |
US6833423B2 (en) | 2002-06-18 | 2004-12-21 | Bayer Polymers Llc | Moisture-curable, polyether urethanes with reactive silane groups and their use as sealants, adhesives and coatings |
DE10232868A1 (de) * | 2002-07-19 | 2004-02-05 | Oxeno Olefinchemie Gmbh | Feinporiger Katalysator und Verfahren zur Hydrierung von aromatischen Verbindungen |
US6946509B2 (en) * | 2002-09-20 | 2005-09-20 | Resolution Specialty Materials Llc | Acrylate-functional alkyd resins having improved dry time |
KR100452329B1 (ko) * | 2002-10-04 | 2004-10-12 | 삼성전자주식회사 | 반도체 코팅설비의 포토레지스트 퍼지 제어장치 |
EP1576150A4 (en) | 2002-10-16 | 2006-05-03 | Univ Texas | METHODS AND COMPOSITIONS FOR INCREASING THE EFFICACY OF ACTIVE SUBSTANCES FROM A BIOLOGICAL VIEWPOINT |
AU2003284676A1 (en) * | 2002-12-02 | 2004-06-23 | Kyoeisha Chemical Co., Ltd. | Curable urethane resin composition |
US6825278B2 (en) * | 2003-01-16 | 2004-11-30 | Resolution Specialty Materials Llc | Modified pressure sensitive adhesive |
US6969716B2 (en) * | 2003-02-07 | 2005-11-29 | Merck Sharp & Dohme Ltd. | 5-phenyl[1,2,4]triazines as ligands for GABA-A α2/α3 receptors for treating anxiety or depression |
US6960619B2 (en) * | 2003-03-06 | 2005-11-01 | Acryfoam Ltd. | Foamable photo-polymerized composition |
US7998403B2 (en) * | 2003-05-05 | 2011-08-16 | The Proctor & Gamble Company | Method of freshening air |
BRPI0506954A (pt) | 2004-01-21 | 2007-06-26 | Firmenich & Cie | vela transparente e método de produzir um éster |
JP4794171B2 (ja) | 2005-01-13 | 2011-10-19 | 株式会社カネカ | 硬化性組成物 |
CN1314530C (zh) | 2005-02-06 | 2007-05-09 | 马兴祥 | 用pvc树脂生产电缆或光缆托架组件的方法 |
US20070012148A1 (en) | 2005-07-14 | 2007-01-18 | Robert Workman | Electronic cutting apparatus and methods for cutting |
US7343834B2 (en) | 2005-07-15 | 2008-03-18 | Howlett Marc K | Beverage holder |
US8372912B2 (en) | 2005-08-12 | 2013-02-12 | Eastman Chemical Company | Polyvinyl chloride compositions |
EP1772480B1 (en) | 2005-10-06 | 2013-12-04 | Henkel AG & Co. KGaA | Reduction of transfer of vibrations |
US7758885B2 (en) * | 2005-11-14 | 2010-07-20 | Coloplast A/S | Cleansing lotion with moisturising, protecting and odor controlling agents and cloth comprising said lotion |
US7754198B2 (en) * | 2005-12-02 | 2010-07-13 | Whitehead Kenneth R | Aroma-releasing polymeric gel matrix |
DE102006001795A1 (de) | 2006-01-12 | 2007-07-19 | Oxeno Olefinchemie Gmbh | Terephthalsäuredialkylester und deren Verwendung |
MX2008011848A (es) * | 2006-03-14 | 2008-09-29 | Procter & Gamble | Lampara decorativa. |
DE102006037317A1 (de) | 2006-08-08 | 2008-02-14 | Celanese Emulsions Gmbh | Vinylestercopolymer-Dispersionen, Verfahren zu deren Herstellung und Verwendung |
CA2661168C (en) * | 2006-08-30 | 2011-11-08 | Eastman Chemical Company | Terephthalates as plasticizers in vinyl acetate polymer compositions |
WO2008027434A2 (en) * | 2006-08-30 | 2008-03-06 | Eastman Chemical Company | Fragrance fixatives |
CA2661173C (en) * | 2006-08-30 | 2012-08-28 | Eastman Chemical Company | Sealant compositions having a novel plasticizer |
US7361779B1 (en) | 2007-04-18 | 2008-04-22 | Eastman Chemical Company | Low-melting mixtures of di-n-butyl and diisobutyl terephthalate |
-
2005
- 2005-08-12 US US11/202,543 patent/US8372912B2/en active Active
-
2006
- 2006-08-10 WO PCT/US2006/031465 patent/WO2007021987A1/en active Application Filing
- 2006-08-10 CA CA2617786A patent/CA2617786C/en not_active Expired - Fee Related
- 2006-08-10 CN CN200680029111.9A patent/CN101238175B/zh active Active
- 2006-08-10 JP JP2008526248A patent/JP5442992B2/ja active Active
- 2006-08-10 EP EP06801312A patent/EP1913069A1/en not_active Withdrawn
-
2008
- 2008-03-07 NO NO20081219A patent/NO20081219L/no not_active Application Discontinuation
-
2013
- 2013-01-24 US US13/749,225 patent/US9388293B2/en active Active
- 2013-01-30 JP JP2013015730A patent/JP5775102B2/ja not_active Expired - Fee Related
-
2014
- 2014-09-10 JP JP2014184207A patent/JP5912157B2/ja active Active
Also Published As
Publication number | Publication date |
---|---|
JP2013076096A (ja) | 2013-04-25 |
US9388293B2 (en) | 2016-07-12 |
US20130137789A1 (en) | 2013-05-30 |
CN101238175B (zh) | 2016-04-20 |
US20070037926A1 (en) | 2007-02-15 |
WO2007021987A1 (en) | 2007-02-22 |
CA2617786A1 (en) | 2007-02-22 |
JP5775102B2 (ja) | 2015-09-09 |
NO20081219L (no) | 2008-03-07 |
EP1913069A1 (en) | 2008-04-23 |
CN101238175A (zh) | 2008-08-06 |
JP2014224275A (ja) | 2014-12-04 |
JP2009504851A (ja) | 2009-02-05 |
JP5442992B2 (ja) | 2014-03-19 |
US8372912B2 (en) | 2013-02-12 |
CA2617786C (en) | 2011-07-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5912157B2 (ja) | ポリ塩化ビニル組成物 | |
US9365695B2 (en) | Polymer compositions comprising terephthalates | |
EP2658728B1 (en) | Blends of dibenzoate plasticizers | |
JP5584121B2 (ja) | 低揮発性有機分の粘度低下剤 | |
CN116769263A (zh) | 改进的无邻苯二甲酸酯的聚氯乙烯增塑溶胶组合物 | |
CN107690447B (zh) | 增塑剂组合物 | |
JP5080221B2 (ja) | 低彩色泡状組成物 | |
US9340658B2 (en) | Low-volatility plasticizer blends | |
CN114867775B (zh) | 氯乙烯树脂组合物 | |
EP3877460A1 (en) | Plasticizer blends | |
US8022127B2 (en) | Plastisols containing glycerol esters as plasticizers | |
JP2020500996A (ja) | 可塑剤組成物 | |
JP7553614B2 (ja) | 可塑剤組成物、およびこれを含む塩化ビニル樹脂組成物 | |
GODWIN | Exxon Chemical Company, Basic Chemicals and Intermediates Technology, 5200 Bayway Drive, Baytown Texas 77586 | |
KR20070009837A (ko) | 2,2,4-트리메틸-1,3-펜탄디올 디에스테르계 가소제 조성물및 이를 포함하는 pvc계 고분자 수지 조성물 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20141001 |
|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20141001 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20150812 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20150908 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20151208 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20160301 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20160331 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 5912157 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |