KR20150003226A - 몰질량이 낮은 1,4:3,6-디안하이드로헥시톨의 에스테르에 기반한 겔화 촉진제를 포함하는 가소제 조성물 - Google Patents
몰질량이 낮은 1,4:3,6-디안하이드로헥시톨의 에스테르에 기반한 겔화 촉진제를 포함하는 가소제 조성물 Download PDFInfo
- Publication number
- KR20150003226A KR20150003226A KR1020147030324A KR20147030324A KR20150003226A KR 20150003226 A KR20150003226 A KR 20150003226A KR 1020147030324 A KR1020147030324 A KR 1020147030324A KR 20147030324 A KR20147030324 A KR 20147030324A KR 20150003226 A KR20150003226 A KR 20150003226A
- Authority
- KR
- South Korea
- Prior art keywords
- dianhydrohexitol
- polymer
- ester
- composition
- weight
- 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.)
- Ceased
Links
- 150000002148 esters Chemical class 0.000 title claims abstract description 71
- 239000000203 mixture Substances 0.000 title claims description 97
- 239000004014 plasticizer Substances 0.000 title description 67
- 229920000642 polymer Polymers 0.000 claims abstract description 112
- 150000001875 compounds Chemical class 0.000 claims abstract description 37
- 239000002253 acid Substances 0.000 claims abstract description 22
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims abstract description 21
- -1 ester compound Chemical class 0.000 claims abstract description 18
- 150000005690 diesters Chemical class 0.000 claims abstract description 17
- 229960002479 isosorbide Drugs 0.000 claims abstract description 16
- KLDXJTOLSGUMSJ-JGWLITMVSA-N Isosorbide Chemical compound O[C@@H]1CO[C@@H]2[C@@H](O)CO[C@@H]21 KLDXJTOLSGUMSJ-JGWLITMVSA-N 0.000 claims abstract description 11
- 150000007513 acids Chemical class 0.000 claims abstract description 11
- 239000003349 gelling agent Substances 0.000 claims abstract description 11
- 239000000470 constituent Substances 0.000 claims abstract description 8
- 238000000034 method Methods 0.000 claims description 47
- 239000004800 polyvinyl chloride Substances 0.000 claims description 42
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 41
- 238000002156 mixing Methods 0.000 claims description 27
- 238000000576 coating method Methods 0.000 claims description 17
- 238000009472 formulation Methods 0.000 claims description 17
- 239000011248 coating agent Substances 0.000 claims description 16
- 230000008569 process Effects 0.000 claims description 16
- 125000004432 carbon atom Chemical group C* 0.000 claims description 15
- 238000007493 shaping process Methods 0.000 claims description 15
- 125000004185 ester group Chemical group 0.000 claims description 14
- 239000000843 powder Substances 0.000 claims description 13
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- GWYFCOCPABKNJV-UHFFFAOYSA-M 3-Methylbutanoic acid Natural products CC(C)CC([O-])=O GWYFCOCPABKNJV-UHFFFAOYSA-M 0.000 claims description 11
- GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 claims description 11
- 230000000930 thermomechanical effect Effects 0.000 claims description 11
- 238000010438 heat treatment Methods 0.000 claims description 10
- 238000003490 calendering Methods 0.000 claims description 7
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 6
- 229920002472 Starch Polymers 0.000 claims description 5
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims description 5
- 235000019698 starch Nutrition 0.000 claims description 5
- 229920002554 vinyl polymer Polymers 0.000 claims description 5
- 239000004952 Polyamide Substances 0.000 claims description 4
- 229920000058 polyacrylate Polymers 0.000 claims description 4
- 229920002647 polyamide Polymers 0.000 claims description 4
- 229920000728 polyester Polymers 0.000 claims description 4
- 229920002635 polyurethane Polymers 0.000 claims description 4
- 239000004814 polyurethane Substances 0.000 claims description 4
- 238000007598 dipping method Methods 0.000 claims description 3
- IKTVJWFFAVUMNE-UHFFFAOYSA-N pentanoic acid;propanoic acid Chemical compound CCC(O)=O.CCCCC(O)=O IKTVJWFFAVUMNE-UHFFFAOYSA-N 0.000 claims description 3
- 238000001175 rotational moulding Methods 0.000 claims description 3
- CFVLXIFIKDTTIG-UHFFFAOYSA-N 2-methylpropanoic acid;pentanoic acid Chemical compound CC(C)C(O)=O.CCCCC(O)=O CFVLXIFIKDTTIG-UHFFFAOYSA-N 0.000 claims description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims description 2
- RFBZVIDYTKNASZ-UHFFFAOYSA-N butanoic acid;2-methylpropanoic acid Chemical compound CCCC(O)=O.CC(C)C(O)=O RFBZVIDYTKNASZ-UHFFFAOYSA-N 0.000 claims description 2
- OZSVFZAVFRWFAY-UHFFFAOYSA-N butanoic acid;hexanoic acid Chemical compound CCCC(O)=O.CCCCCC(O)=O OZSVFZAVFRWFAY-UHFFFAOYSA-N 0.000 claims description 2
- SZORMCBRRGPWKG-UHFFFAOYSA-N butanoic acid;pentanoic acid Chemical compound CCCC(O)=O.CCCCC(O)=O SZORMCBRRGPWKG-UHFFFAOYSA-N 0.000 claims description 2
- PXGPQCBSBQOPLZ-UHFFFAOYSA-N butanoic acid;propanoic acid Chemical compound CCC(O)=O.CCCC(O)=O PXGPQCBSBQOPLZ-UHFFFAOYSA-N 0.000 claims description 2
- ATBGUXLYDPOXID-UHFFFAOYSA-N hexanoic acid;2-methylpropanoic acid Chemical compound CC(C)C(O)=O.CCCCCC(O)=O ATBGUXLYDPOXID-UHFFFAOYSA-N 0.000 claims description 2
- MBEGHXRSTJGPKQ-UHFFFAOYSA-N hexanoic acid;pentanoic acid Chemical compound CCCCC(O)=O.CCCCCC(O)=O MBEGHXRSTJGPKQ-UHFFFAOYSA-N 0.000 claims description 2
- 229920005992 thermoplastic resin Polymers 0.000 claims description 2
- KLDXJTOLSGUMSJ-BXKVDMCESA-N (3s,3as,6s,6as)-2,3,3a,5,6,6a-hexahydrofuro[3,2-b]furan-3,6-diol Chemical compound O[C@H]1CO[C@H]2[C@@H](O)CO[C@H]21 KLDXJTOLSGUMSJ-BXKVDMCESA-N 0.000 claims 3
- VJHKZGQPLJDVCL-UHFFFAOYSA-N hexanoic acid;3-methylbutanoic acid Chemical compound CC(C)CC(O)=O.CCCCCC(O)=O VJHKZGQPLJDVCL-UHFFFAOYSA-N 0.000 claims 1
- CFXKYNOBOMFSBI-UHFFFAOYSA-N hexanoic acid;propanoic acid Chemical compound CCC(O)=O.CCCCCC(O)=O CFXKYNOBOMFSBI-UHFFFAOYSA-N 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 abstract description 6
- 150000002314 glycerols Chemical class 0.000 abstract 1
- RGXCTRIQQODGIZ-UHFFFAOYSA-O isodesmosine Chemical compound OC(=O)C(N)CCCC[N+]1=CC(CCC(N)C(O)=O)=CC(CCC(N)C(O)=O)=C1CCCC(N)C(O)=O RGXCTRIQQODGIZ-UHFFFAOYSA-O 0.000 description 38
- 238000001879 gelation Methods 0.000 description 36
- 238000012360 testing method Methods 0.000 description 29
- YCZJVRCZIPDYHH-UHFFFAOYSA-N ditridecyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCCCCCC YCZJVRCZIPDYHH-UHFFFAOYSA-N 0.000 description 24
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 20
- 239000000047 product Substances 0.000 description 19
- 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 description 17
- 239000004806 diisononylester Substances 0.000 description 16
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 15
- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 description 15
- 229920001944 Plastisol Polymers 0.000 description 11
- 239000004999 plastisol Substances 0.000 description 11
- 230000008901 benefit Effects 0.000 description 10
- 230000008859 change Effects 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 8
- 230000008014 freezing Effects 0.000 description 8
- 238000007710 freezing Methods 0.000 description 8
- 238000012545 processing Methods 0.000 description 8
- 150000001298 alcohols Chemical class 0.000 description 7
- 238000001125 extrusion Methods 0.000 description 7
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 7
- WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Natural products CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 6
- 229920012485 Plasticized Polyvinyl chloride Polymers 0.000 description 6
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 6
- MGWAVDBGNNKXQV-UHFFFAOYSA-N diisobutyl phthalate Chemical compound CC(C)COC(=O)C1=CC=CC=C1C(=O)OCC(C)C MGWAVDBGNNKXQV-UHFFFAOYSA-N 0.000 description 6
- 238000005886 esterification reaction Methods 0.000 description 6
- 238000005259 measurement Methods 0.000 description 6
- 229920003023 plastic Polymers 0.000 description 6
- 239000004033 plastic Substances 0.000 description 6
- 229920006395 saturated elastomer Polymers 0.000 description 6
- 239000012855 volatile organic compound Substances 0.000 description 6
- KLDXJTOLSGUMSJ-UNTFVMJOSA-N (3s,3ar,6s,6ar)-2,3,3a,5,6,6a-hexahydrofuro[3,2-b]furan-3,6-diol Chemical compound O[C@H]1CO[C@@H]2[C@@H](O)CO[C@@H]21 KLDXJTOLSGUMSJ-UNTFVMJOSA-N 0.000 description 5
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 5
- 239000000654 additive Substances 0.000 description 5
- 238000003860 storage Methods 0.000 description 5
- HNDYULRADYGBDU-UHFFFAOYSA-N 8-methylnonyl benzoate Chemical compound CC(C)CCCCCCCOC(=O)C1=CC=CC=C1 HNDYULRADYGBDU-UHFFFAOYSA-N 0.000 description 4
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 4
- 150000001735 carboxylic acids Chemical class 0.000 description 4
- 238000013329 compounding Methods 0.000 description 4
- 230000001143 conditioned effect Effects 0.000 description 4
- 238000002425 crystallisation Methods 0.000 description 4
- 230000008025 crystallization Effects 0.000 description 4
- QSAWQNUELGIYBC-UHFFFAOYSA-N cyclohexane-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCCCC1C(O)=O QSAWQNUELGIYBC-UHFFFAOYSA-N 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 125000005498 phthalate group Chemical class 0.000 description 4
- ZDPHROOEEOARMN-UHFFFAOYSA-N undecanoic acid Chemical compound CCCCCCCCCCC(O)=O ZDPHROOEEOARMN-UHFFFAOYSA-N 0.000 description 4
- UADWUILHKRXHMM-UHFFFAOYSA-N 2-ethylhexyl benzoate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1 UADWUILHKRXHMM-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 description 3
- 125000003158 alcohol group Chemical group 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 230000009477 glass transition Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 3
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- WQEPLUUGTLDZJY-UHFFFAOYSA-N pentadecanoic acid Chemical compound CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 3
- 229940005605 valeric acid Drugs 0.000 description 3
- XYHKNCXZYYTLRG-UHFFFAOYSA-N 1h-imidazole-2-carbaldehyde Chemical compound O=CC1=NC=CN1 XYHKNCXZYYTLRG-UHFFFAOYSA-N 0.000 description 2
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000003463 adsorbent Substances 0.000 description 2
- 238000005273 aeration Methods 0.000 description 2
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 2
- GONOPSZTUGRENK-UHFFFAOYSA-N benzyl(trichloro)silane Chemical compound Cl[Si](Cl)(Cl)CC1=CC=CC=C1 GONOPSZTUGRENK-UHFFFAOYSA-N 0.000 description 2
- 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 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- QYQADNCHXSEGJT-UHFFFAOYSA-N cyclohexane-1,1-dicarboxylate;hydron Chemical class OC(=O)C1(C(O)=O)CCCCC1 QYQADNCHXSEGJT-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 150000002009 diols Chemical class 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000012760 heat stabilizer Substances 0.000 description 2
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 150000002763 monocarboxylic acids Chemical class 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000000565 sealant Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 230000035882 stress Effects 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 229920001059 synthetic polymer Polymers 0.000 description 2
- 239000003017 thermal stabilizer Substances 0.000 description 2
- 238000003856 thermoforming Methods 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 description 2
- PXGZQGDTEZPERC-UHFFFAOYSA-N 1,4-cyclohexanedicarboxylic acid Chemical compound OC(=O)C1CCC(C(O)=O)CC1 PXGZQGDTEZPERC-UHFFFAOYSA-N 0.000 description 1
- ZWMHQUSHSJEGOI-UHFFFAOYSA-N 1-(2-methylpropanoyloxy)hexyl 2-methylpropanoate Chemical compound CCCCCC(OC(=O)C(C)C)OC(=O)C(C)C ZWMHQUSHSJEGOI-UHFFFAOYSA-N 0.000 description 1
- GYSCBCSGKXNZRH-UHFFFAOYSA-N 1-benzothiophene-2-carboxamide Chemical compound C1=CC=C2SC(C(=O)N)=CC2=C1 GYSCBCSGKXNZRH-UHFFFAOYSA-N 0.000 description 1
- NZUJVBSYQXETNF-UHFFFAOYSA-N 10-dml Natural products CCC1OC(=O)C(C)C(O)C(C)CC(C)C(=O)C=CC1C NZUJVBSYQXETNF-UHFFFAOYSA-N 0.000 description 1
- MROVDGPAQMTQBF-UHFFFAOYSA-N 2-methylpropanoic acid;propanoic acid Chemical compound CCC(O)=O.CC(C)C(O)=O MROVDGPAQMTQBF-UHFFFAOYSA-N 0.000 description 1
- AWQSAIIDOMEEOD-UHFFFAOYSA-N 5,5-Dimethyl-4-(3-oxobutyl)dihydro-2(3H)-furanone Chemical compound CC(=O)CCC1CC(=O)OC1(C)C AWQSAIIDOMEEOD-UHFFFAOYSA-N 0.000 description 1
- QZCLKYGREBVARF-UHFFFAOYSA-N Acetyl tributyl citrate Chemical compound CCCCOC(=O)CC(C(=O)OCCCC)(OC(C)=O)CC(=O)OCCCC QZCLKYGREBVARF-UHFFFAOYSA-N 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 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
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- FBPFZTCFMRRESA-ZXXMMSQZSA-N D-iditol Chemical compound OC[C@@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-ZXXMMSQZSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 239000004594 Masterbatch (MB) Substances 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 239000012963 UV stabilizer Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000000809 air pollutant Substances 0.000 description 1
- 231100001243 air pollutant Toxicity 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- AMFJQTQGNFWVNR-UHFFFAOYSA-N butanoic acid;decanoic acid Chemical compound CCCC(O)=O.CCCCCCCCCC(O)=O AMFJQTQGNFWVNR-UHFFFAOYSA-N 0.000 description 1
- KEJOBUDURBXRJY-UHFFFAOYSA-N butanoic acid;nonanoic acid Chemical compound CCCC(O)=O.CCCCCCCCC(O)=O KEJOBUDURBXRJY-UHFFFAOYSA-N 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000004320 controlled atmosphere Methods 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- CORTZJMILBLCKC-UHFFFAOYSA-N decanoic acid;dodecanoic acid Chemical compound CCCCCCCCCC(O)=O.CCCCCCCCCCCC(O)=O CORTZJMILBLCKC-UHFFFAOYSA-N 0.000 description 1
- PEDZITIZNRJXHF-UHFFFAOYSA-N decanoic acid;heptanoic acid Chemical compound CCCCCCC(O)=O.CCCCCCCCCC(O)=O PEDZITIZNRJXHF-UHFFFAOYSA-N 0.000 description 1
- IYSQFQAYCSYJRB-UHFFFAOYSA-N decanoic acid;hexanoic acid Chemical compound CCCCCC(O)=O.CCCCCCCCCC(O)=O IYSQFQAYCSYJRB-UHFFFAOYSA-N 0.000 description 1
- OJCIECFVKMNUAG-UHFFFAOYSA-N decanoic acid;undecanoic acid Chemical compound CCCCCCCCCC(O)=O.CCCCCCCCCCC(O)=O OJCIECFVKMNUAG-UHFFFAOYSA-N 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- FBTFEMIXBHYMCH-UHFFFAOYSA-N dodecanoic acid;heptanoic acid Chemical compound CCCCCCC(O)=O.CCCCCCCCCCCC(O)=O FBTFEMIXBHYMCH-UHFFFAOYSA-N 0.000 description 1
- MDHQNNQPSPMQDQ-UHFFFAOYSA-N dodecanoic acid;nonanoic acid Chemical compound CCCCCCCCC(O)=O.CCCCCCCCCCCC(O)=O MDHQNNQPSPMQDQ-UHFFFAOYSA-N 0.000 description 1
- PYVNUZAVACSANL-UHFFFAOYSA-N dodecanoic acid;octanoic acid Chemical compound CCCCCCCC(O)=O.CCCCCCCCCCCC(O)=O PYVNUZAVACSANL-UHFFFAOYSA-N 0.000 description 1
- QKQGIUQLBKCRQY-UHFFFAOYSA-N dodecanoic acid;undecanoic acid Chemical compound CCCCCCCCCCC(O)=O.CCCCCCCCCCCC(O)=O QKQGIUQLBKCRQY-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000482 effect on migration Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000010101 extrusion blow moulding Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 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 description 1
- 239000001087 glyceryl triacetate Substances 0.000 description 1
- 235000013773 glyceryl triacetate Nutrition 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- ZDCCVLOYPXQYKU-UHFFFAOYSA-N heptanoic acid;hexanoic acid Chemical compound CCCCCC(O)=O.CCCCCCC(O)=O ZDCCVLOYPXQYKU-UHFFFAOYSA-N 0.000 description 1
- SKCMCXVYSJRFPA-UHFFFAOYSA-N heptanoic acid;nonanoic acid Chemical compound CCCCCCC(O)=O.CCCCCCCCC(O)=O SKCMCXVYSJRFPA-UHFFFAOYSA-N 0.000 description 1
- JBGMARMAOJZNSL-UHFFFAOYSA-N heptanoic acid;octanoic acid Chemical compound CCCCCCC(O)=O.CCCCCCCC(O)=O JBGMARMAOJZNSL-UHFFFAOYSA-N 0.000 description 1
- HKVJCWPEYIMZNQ-UHFFFAOYSA-N heptanoic acid;undecanoic acid Chemical compound CCCCCCC(O)=O.CCCCCCCCCCC(O)=O HKVJCWPEYIMZNQ-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-UHFFFAOYSA-N hexane-1,2,3,4,5,6-hexol Chemical compound OCC(O)C(O)C(O)C(O)CO FBPFZTCFMRRESA-UHFFFAOYSA-N 0.000 description 1
- NDTKJPJWXDRYIY-UHFFFAOYSA-N hexanoic acid;octanoic acid Chemical compound CCCCCC(O)=O.CCCCCCCC(O)=O NDTKJPJWXDRYIY-UHFFFAOYSA-N 0.000 description 1
- ARQBMFJUNGMLFR-UHFFFAOYSA-N hexanoic acid;undecanoic acid Chemical compound CCCCCC(O)=O.CCCCCCCCCCC(O)=O ARQBMFJUNGMLFR-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 239000002649 leather substitute Substances 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- ZPVFWPFBNIEHGJ-UHFFFAOYSA-N n-hexyl methyl ketone Natural products CCCCCCC(C)=O ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 0.000 description 1
- DBVFFJULYPMFJD-UHFFFAOYSA-N nonanoic acid;octanoic acid Chemical compound CCCCCCCC(O)=O.CCCCCCCCC(O)=O DBVFFJULYPMFJD-UHFFFAOYSA-N 0.000 description 1
- WBKSEEJVLUYBSI-UHFFFAOYSA-N nonanoic acid;pentanoic acid Chemical compound CCCCC(O)=O.CCCCCCCCC(O)=O WBKSEEJVLUYBSI-UHFFFAOYSA-N 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical compound CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 description 1
- BFEFRVOLEFSAOI-UHFFFAOYSA-N octanoic acid;pentanoic acid Chemical compound CCCCC(O)=O.CCCCCCCC(O)=O BFEFRVOLEFSAOI-UHFFFAOYSA-N 0.000 description 1
- MTLLZXFFVIPJAJ-UHFFFAOYSA-N octanoic acid;undecanoic acid Chemical compound CCCCCCCC(O)=O.CCCCCCCCCCC(O)=O MTLLZXFFVIPJAJ-UHFFFAOYSA-N 0.000 description 1
- BGGOGZBJMMLVNJ-UHFFFAOYSA-N pentanoic acid;undecanoic acid Chemical compound CCCCC(O)=O.CCCCCCCCCCC(O)=O BGGOGZBJMMLVNJ-UHFFFAOYSA-N 0.000 description 1
- 239000008029 phthalate plasticizer Substances 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 150000003021 phthalic acid derivatives Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000009182 swimming Effects 0.000 description 1
- 238000003878 thermal aging Methods 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 229960002622 triacetin Drugs 0.000 description 1
Images
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
- C08K5/15—Heterocyclic compounds having oxygen in the ring
- C08K5/151—Heterocyclic compounds having oxygen in the ring having one oxygen atom in the ring
- C08K5/1535—Five-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0016—Plasticisers
-
- 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
-
- 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
- C08K5/11—Esters; Ether-esters of acyclic 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
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D127/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers
- C09D127/02—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
- C09D127/04—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C09D127/06—Homopolymers or copolymers of vinyl chloride
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/63—Additives non-macromolecular organic
-
- 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)
- Organic Chemistry (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR1254086A FR2990210B1 (fr) | 2012-05-03 | 2012-05-03 | Compositions plastifiantes comprenant des accelerateurs de gelification a base d'ester de 1,4 : 3,6-dianhydrohexitol de faible poids molaire |
| FR1254086 | 2012-05-03 | ||
| PCT/FR2013/050967 WO2013164545A2 (fr) | 2012-05-03 | 2013-05-02 | Compositions plastifiantes comprenant des accelerateurs de gelification a base d'ester de 1,4 : 3,6-dianhydrohexitol de faible poids molaire |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20150003226A true KR20150003226A (ko) | 2015-01-08 |
Family
ID=48577102
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020147030324A Ceased KR20150003226A (ko) | 2012-05-03 | 2013-05-02 | 몰질량이 낮은 1,4:3,6-디안하이드로헥시톨의 에스테르에 기반한 겔화 촉진제를 포함하는 가소제 조성물 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US10005894B2 (enExample) |
| EP (1) | EP2844691B1 (enExample) |
| JP (1) | JP6064035B2 (enExample) |
| KR (1) | KR20150003226A (enExample) |
| CN (1) | CN104271653B (enExample) |
| FR (1) | FR2990210B1 (enExample) |
| IN (1) | IN2014DN09169A (enExample) |
| MY (1) | MY172394A (enExample) |
| WO (1) | WO2013164545A2 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20160098453A (ko) * | 2013-12-18 | 2016-08-18 | 아처 다니엘 미드랜드 캄파니 | 이소헥시드 에스테르화에서 색 개체 형성의 조절 |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6219133B2 (ja) * | 2013-11-07 | 2017-10-25 | リケンテクノス株式会社 | 医療用塩化ビニル樹脂組成物およびそれからなる医療用器具 |
| FR3021329B1 (fr) * | 2014-05-26 | 2020-05-29 | Roquette Freres | Substrat methanogene pour la fabrication de biogaz. |
| FR3024735B1 (fr) * | 2014-08-07 | 2016-08-26 | Roquette Freres | Composition plastifiante liquide |
| CN111875899B (zh) * | 2020-06-22 | 2021-04-30 | 安徽滁州德威新材料有限公司 | 一种耐低温柔软弹性注塑组合物及其制备方法和应用 |
| JP2025010076A (ja) * | 2023-07-05 | 2025-01-20 | 花王株式会社 | 可塑剤組成物 |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2315223C (en) | 1997-12-19 | 2010-02-09 | Basf Aktiengesellschaft | Method for hydrogenating benzene polycarboxylic acids or derivatives thereof by using a catalyst containing macropores |
| AU751753B2 (en) * | 1998-03-04 | 2002-08-29 | Ato B.V. | Bicyclooctane derivatives as plasticisers |
| DE19927977A1 (de) | 1999-06-18 | 2000-12-21 | Basf Ag | Verwendung von Cyclohexanpolycarbonsäuren als Weichmacher zur Herstellung toxikologisch günstig zu bewertender Kunststoffe |
| US7291748B2 (en) * | 2005-07-28 | 2007-11-06 | Basf Corporation | C10/C7 ester mixtures based on 2-propylheptanol |
| US20100257657A1 (en) * | 2006-03-01 | 2010-10-14 | Smarthealth, Inc. | Polylactic acid gloves and methods of manufacturing same |
| DE102007006442A1 (de) * | 2007-02-05 | 2008-08-07 | Evonik Oxeno Gmbh | Gemisch von Diestern von Dianhydrohexitolderivaten mit Carbonsäuren der Summenformel C8H17COOH, Verfahren zur Herstellung dieser Diester und Verwendung dieser Gemische |
| DE102007028702A1 (de) * | 2007-06-21 | 2008-12-24 | Evonik Oxeno Gmbh | Verfahren zur Herstellung von Dianhydrohexitol-Diestern |
| DE102009028975A1 (de) * | 2009-08-28 | 2011-03-03 | Evonik Oxeno Gmbh | Esterderivate der 2,5-Furandicarbonsäure und ihre Verwendung als Weichmacher |
| JP5251857B2 (ja) * | 2009-12-16 | 2013-07-31 | コニカミノルタアドバンストレイヤー株式会社 | 光学フィルム |
| WO2011097443A1 (en) * | 2010-02-04 | 2011-08-11 | Elementis Specialties,Inc | Dianhydrohexitol diester coalescing agent |
| DE102010002856A1 (de) * | 2010-03-15 | 2011-09-15 | Kuraray Europe Gmbh | Verwendung von Isosorbiddiestern als Weichmacher für Zwischenschichtfolien aus Polyvinylacetal |
| FR2965814B1 (fr) * | 2010-10-08 | 2012-11-16 | Roquette Freres | Plastification de polyesters aliphatiques par des esters alkyliques de dianhydrohexitols |
| DE102011089493A1 (de) * | 2011-12-21 | 2013-06-27 | Evonik Industries Ag | Dianhydrohexitoldiestergemisch NMR |
-
2012
- 2012-05-03 FR FR1254086A patent/FR2990210B1/fr active Active
-
2013
- 2013-05-02 JP JP2015509475A patent/JP6064035B2/ja active Active
- 2013-05-02 EP EP13727244.9A patent/EP2844691B1/fr active Active
- 2013-05-02 WO PCT/FR2013/050967 patent/WO2013164545A2/fr not_active Ceased
- 2013-05-02 CN CN201380023380.4A patent/CN104271653B/zh active Active
- 2013-05-02 IN IN9169DEN2014 patent/IN2014DN09169A/en unknown
- 2013-05-02 KR KR1020147030324A patent/KR20150003226A/ko not_active Ceased
- 2013-05-02 MY MYPI2014003090A patent/MY172394A/en unknown
- 2013-05-02 US US14/397,968 patent/US10005894B2/en active Active
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20160098453A (ko) * | 2013-12-18 | 2016-08-18 | 아처 다니엘 미드랜드 캄파니 | 이소헥시드 에스테르화에서 색 개체 형성의 조절 |
Also Published As
| Publication number | Publication date |
|---|---|
| CN104271653A (zh) | 2015-01-07 |
| WO2013164545A2 (fr) | 2013-11-07 |
| WO2013164545A3 (fr) | 2014-01-03 |
| JP6064035B2 (ja) | 2017-01-18 |
| EP2844691B1 (fr) | 2019-08-14 |
| CN104271653B (zh) | 2017-04-19 |
| US20150125613A1 (en) | 2015-05-07 |
| FR2990210A1 (fr) | 2013-11-08 |
| MY172394A (en) | 2019-11-22 |
| FR2990210B1 (fr) | 2014-05-02 |
| US10005894B2 (en) | 2018-06-26 |
| EP2844691A2 (fr) | 2015-03-11 |
| IN2014DN09169A (enExample) | 2015-07-10 |
| JP2015516009A (ja) | 2015-06-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP2231763B1 (en) | Co-plasticizer systems | |
| EP2678322B1 (de) | Pentylester der furandicarbonsäure als weichmacher | |
| JP5912157B2 (ja) | ポリ塩化ビニル組成物 | |
| CN101107306B (zh) | 在增塑剂组合物中或涉及增塑剂组合物的改进 | |
| KR20150003226A (ko) | 몰질량이 낮은 1,4:3,6-디안하이드로헥시톨의 에스테르에 기반한 겔화 촉진제를 포함하는 가소제 조성물 | |
| US20080200595A1 (en) | Esterified Fatty Acids for Pvc Plasticization | |
| EP3473669B1 (en) | Method of controlling plastisol viscosity | |
| JP6379101B2 (ja) | 1,4:3,6−ジアンヒドロヘキシトールジエステル組成物を製造する方法 | |
| US10179847B2 (en) | Liquid plasticising composition | |
| 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 | |
| TW202313552A (zh) | 包含1,2,4-環己烷三羧酸之三戊酯之塑化劑組成物 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0105 | International application |
Patent event date: 20141029 Patent event code: PA01051R01D Comment text: International Patent Application |
|
| PG1501 | Laying open of application | ||
| PA0201 | Request for examination |
Patent event code: PA02012R01D Patent event date: 20180426 Comment text: Request for Examination of Application |
|
| E902 | Notification of reason for refusal | ||
| PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20191125 Patent event code: PE09021S01D |
|
| E601 | Decision to refuse application | ||
| PE0601 | Decision on rejection of patent |
Patent event date: 20200708 Comment text: Decision to Refuse Application Patent event code: PE06012S01D Patent event date: 20191125 Comment text: Notification of reason for refusal Patent event code: PE06011S01I |