SK84799A3 - Use of polyalcohols as polymer stabilisers - Google Patents
Use of polyalcohols as polymer stabilisers Download PDFInfo
- Publication number
- SK84799A3 SK84799A3 SK847-99A SK84799A SK84799A3 SK 84799 A3 SK84799 A3 SK 84799A3 SK 84799 A SK84799 A SK 84799A SK 84799 A3 SK84799 A3 SK 84799A3
- Authority
- SK
- Slovakia
- Prior art keywords
- polymer
- parts
- use according
- inulin
- polyol
- Prior art date
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- 229920000642 polymer Polymers 0.000 title claims abstract description 30
- 150000005846 sugar alcohols Polymers 0.000 title claims abstract description 14
- 239000003381 stabilizer Substances 0.000 title claims description 27
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 claims abstract description 22
- JYJIGFIDKWBXDU-MNNPPOADSA-N inulin Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)OC[C@]1(OC[C@]2(OC[C@]3(OC[C@]4(OC[C@]5(OC[C@]6(OC[C@]7(OC[C@]8(OC[C@]9(OC[C@]%10(OC[C@]%11(OC[C@]%12(OC[C@]%13(OC[C@]%14(OC[C@]%15(OC[C@]%16(OC[C@]%17(OC[C@]%18(OC[C@]%19(OC[C@]%20(OC[C@]%21(OC[C@]%22(OC[C@]%23(OC[C@]%24(OC[C@]%25(OC[C@]%26(OC[C@]%27(OC[C@]%28(OC[C@]%29(OC[C@]%30(OC[C@]%31(OC[C@]%32(OC[C@]%33(OC[C@]%34(OC[C@]%35(OC[C@]%36(O[C@@H]%37[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O%37)O)[C@H]([C@H](O)[C@@H](CO)O%36)O)[C@H]([C@H](O)[C@@H](CO)O%35)O)[C@H]([C@H](O)[C@@H](CO)O%34)O)[C@H]([C@H](O)[C@@H](CO)O%33)O)[C@H]([C@H](O)[C@@H](CO)O%32)O)[C@H]([C@H](O)[C@@H](CO)O%31)O)[C@H]([C@H](O)[C@@H](CO)O%30)O)[C@H]([C@H](O)[C@@H](CO)O%29)O)[C@H]([C@H](O)[C@@H](CO)O%28)O)[C@H]([C@H](O)[C@@H](CO)O%27)O)[C@H]([C@H](O)[C@@H](CO)O%26)O)[C@H]([C@H](O)[C@@H](CO)O%25)O)[C@H]([C@H](O)[C@@H](CO)O%24)O)[C@H]([C@H](O)[C@@H](CO)O%23)O)[C@H]([C@H](O)[C@@H](CO)O%22)O)[C@H]([C@H](O)[C@@H](CO)O%21)O)[C@H]([C@H](O)[C@@H](CO)O%20)O)[C@H]([C@H](O)[C@@H](CO)O%19)O)[C@H]([C@H](O)[C@@H](CO)O%18)O)[C@H]([C@H](O)[C@@H](CO)O%17)O)[C@H]([C@H](O)[C@@H](CO)O%16)O)[C@H]([C@H](O)[C@@H](CO)O%15)O)[C@H]([C@H](O)[C@@H](CO)O%14)O)[C@H]([C@H](O)[C@@H](CO)O%13)O)[C@H]([C@H](O)[C@@H](CO)O%12)O)[C@H]([C@H](O)[C@@H](CO)O%11)O)[C@H]([C@H](O)[C@@H](CO)O%10)O)[C@H]([C@H](O)[C@@H](CO)O9)O)[C@H]([C@H](O)[C@@H](CO)O8)O)[C@H]([C@H](O)[C@@H](CO)O7)O)[C@H]([C@H](O)[C@@H](CO)O6)O)[C@H]([C@H](O)[C@@H](CO)O5)O)[C@H]([C@H](O)[C@@H](CO)O4)O)[C@H]([C@H](O)[C@@H](CO)O3)O)[C@H]([C@H](O)[C@@H](CO)O2)O)[C@@H](O)[C@H](O)[C@@H](CO)O1 JYJIGFIDKWBXDU-MNNPPOADSA-N 0.000 claims abstract description 21
- 229920001202 Inulin Polymers 0.000 claims abstract description 20
- -1 cyclic polyol Chemical class 0.000 claims abstract description 20
- 229940029339 inulin Drugs 0.000 claims abstract description 20
- 229920005862 polyol Polymers 0.000 claims abstract description 17
- 150000003077 polyols Chemical class 0.000 claims abstract description 11
- 229920001169 thermoplastic Polymers 0.000 claims abstract description 9
- 230000018044 dehydration Effects 0.000 claims abstract description 5
- 238000006297 dehydration reaction Methods 0.000 claims abstract description 5
- 229920000157 polyfructose Polymers 0.000 claims abstract description 5
- 239000000203 mixture Substances 0.000 claims description 26
- 125000000129 anionic group Chemical group 0.000 claims description 9
- 241000132519 Galactites Species 0.000 claims description 7
- 239000004927 clay Substances 0.000 claims description 7
- 230000000087 stabilizing effect Effects 0.000 claims description 7
- 239000004698 Polyethylene Substances 0.000 claims description 6
- 235000014633 carbohydrates Nutrition 0.000 claims description 6
- 159000000007 calcium salts Chemical class 0.000 claims description 4
- 239000004743 Polypropylene Substances 0.000 claims description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 3
- 229920000573 polyethylene Polymers 0.000 claims description 3
- 229920001155 polypropylene Polymers 0.000 claims description 3
- 150000003752 zinc compounds Chemical class 0.000 claims description 3
- 229920001577 copolymer Polymers 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 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 claims description 2
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 claims 2
- 229930091371 Fructose Natural products 0.000 claims 2
- 239000005715 Fructose Substances 0.000 claims 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims 2
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims 2
- 239000008103 glucose Substances 0.000 claims 2
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims 1
- 229930006000 Sucrose Natural products 0.000 claims 1
- 239000005720 sucrose Substances 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 abstract description 7
- 229920001971 elastomer Polymers 0.000 abstract description 3
- 230000003019 stabilising effect Effects 0.000 abstract 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 17
- 239000004800 polyvinyl chloride Substances 0.000 description 17
- 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 7
- 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 6
- 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 6
- 229930195725 Mannitol Natural products 0.000 description 6
- 239000000594 mannitol Substances 0.000 description 6
- 235000010355 mannitol Nutrition 0.000 description 6
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 6
- 239000000600 sorbitol Substances 0.000 description 6
- 235000010356 sorbitol Nutrition 0.000 description 6
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 239000000811 xylitol Substances 0.000 description 5
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 5
- 235000010447 xylitol Nutrition 0.000 description 5
- 229960002675 xylitol Drugs 0.000 description 5
- BPXVHIRIPLPOPT-UHFFFAOYSA-N 1,3,5-tris(2-hydroxyethyl)-1,3,5-triazinane-2,4,6-trione Chemical compound OCCN1C(=O)N(CCO)C(=O)N(CCO)C1=O BPXVHIRIPLPOPT-UHFFFAOYSA-N 0.000 description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000011777 magnesium Substances 0.000 description 4
- 239000003607 modifier Substances 0.000 description 4
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- 229910052725 zinc Inorganic materials 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
- 230000009286 beneficial effect Effects 0.000 description 3
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- 239000011575 calcium Substances 0.000 description 3
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 3
- 235000013539 calcium stearate Nutrition 0.000 description 3
- 239000008116 calcium stearate Substances 0.000 description 3
- 150000001720 carbohydrates Chemical class 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 230000006641 stabilisation Effects 0.000 description 3
- 238000011105 stabilization Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical class [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 3
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Chemical class CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 150000004676 glycans Chemical class 0.000 description 2
- 229910001385 heavy metal Inorganic materials 0.000 description 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
- VQHSOMBJVWLPSR-JVCRWLNRSA-N lactitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O VQHSOMBJVWLPSR-JVCRWLNRSA-N 0.000 description 2
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- 231100000252 nontoxic Toxicity 0.000 description 2
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- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
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- 229920002959 polymer blend Polymers 0.000 description 2
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- 150000003751 zinc Chemical class 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- MPCAJMNYNOGXPB-UHFFFAOYSA-N 1,5-anhydrohexitol Chemical class OCC1OCC(O)C(O)C1O MPCAJMNYNOGXPB-UHFFFAOYSA-N 0.000 description 1
- LRQGFQDEQPZDQC-UHFFFAOYSA-N 1-Phenyl-1,3-eicosanedione Chemical compound CCCCCCCCCCCCCCCCCC(=O)CC(=O)C1=CC=CC=C1 LRQGFQDEQPZDQC-UHFFFAOYSA-N 0.000 description 1
- MCHWWJLLPNDHGL-UHFFFAOYSA-N 2,5-bis(hydroxymethyl)oxolane-3,4-diol Chemical class OCC1OC(CO)C(O)C1O MCHWWJLLPNDHGL-UHFFFAOYSA-N 0.000 description 1
- JNYAEWCLZODPBN-UHFFFAOYSA-N 2-(1,2-dihydroxyethyl)oxolane-3,4-diol Chemical class OCC(O)C1OCC(O)C1O JNYAEWCLZODPBN-UHFFFAOYSA-N 0.000 description 1
- KZVAAIRBJJYZOW-UHFFFAOYSA-N 2-(hydroxymethyl)oxolane-3,4-diol Chemical class OCC1OCC(O)C1O KZVAAIRBJJYZOW-UHFFFAOYSA-N 0.000 description 1
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- 150000002646 long chain fatty acid esters Chemical class 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- WIBFFTLQMKKBLZ-SEYXRHQNSA-N n-butyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCCC WIBFFTLQMKKBLZ-SEYXRHQNSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- 229910052755 nonmetal Inorganic materials 0.000 description 1
- 229920001542 oligosaccharide Polymers 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 238000010525 oxidative degradation reaction Methods 0.000 description 1
- DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
- 150000003021 phthalic acid derivatives Chemical class 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 238000012667 polymer degradation Methods 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 229940022860 xylitan Drugs 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 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
- C08K5/15—Heterocyclic compounds having oxygen in the ring
- C08K5/151—Heterocyclic compounds having oxygen in the ring having one oxygen atom in the ring
-
- 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
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)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP96203624 | 1996-12-19 | ||
| PCT/NL1997/000709 WO1998027148A1 (en) | 1996-12-19 | 1997-12-18 | Use of polyalcohols as polymer stabilisers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SK84799A3 true SK84799A3 (en) | 2000-01-18 |
Family
ID=8224725
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK847-99A SK84799A3 (en) | 1996-12-19 | 1997-12-18 | Use of polyalcohols as polymer stabilisers |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US6313203B1 (de) |
| EP (1) | EP0946634B1 (de) |
| JP (1) | JP2001506301A (de) |
| KR (1) | KR20000069558A (de) |
| CN (1) | CN1244880A (de) |
| AT (1) | ATE208802T1 (de) |
| AU (1) | AU5348498A (de) |
| CA (1) | CA2275416A1 (de) |
| DE (1) | DE69708323T2 (de) |
| DK (1) | DK0946634T3 (de) |
| HU (1) | HUP9903831A2 (de) |
| PL (1) | PL334210A1 (de) |
| SK (1) | SK84799A3 (de) |
| TR (1) | TR199901360T2 (de) |
| WO (1) | WO1998027148A1 (de) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10118179A1 (de) * | 2001-04-11 | 2002-10-24 | Baerlocher Gmbh | Stabilisatorkombination für halogenhaltige Polymere und deren Verwendung |
| US20040063826A1 (en) * | 2002-09-30 | 2004-04-01 | Sobieski Robert T. | Halogen-containing vinyl polymer compounds |
| US20040061095A1 (en) * | 2002-09-30 | 2004-04-01 | Sobieski Robert T. | Halogen-containing vinyl polymer stabilizers |
| US7029759B2 (en) * | 2002-09-30 | 2006-04-18 | Omnova Solutions Inc. | Halogen-containing vinyl polymer compositions |
| US20080200600A1 (en) * | 2004-06-23 | 2008-08-21 | Akzo Nobel N. V. | Polymer-Containing Composition, its Preparation and Use |
| CN101942110B (zh) * | 2010-09-06 | 2012-03-21 | 芜湖海螺型材科技股份有限公司 | 一种钙锌复合稳定剂 |
| JP6936435B2 (ja) * | 2017-04-27 | 2021-09-15 | 新日本理化株式会社 | 高温使用時の着色の抑制された塩化ビニル系樹脂組成物 |
| DE102017217312A1 (de) * | 2017-09-28 | 2019-03-28 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Verfahren zur Stabilisierung von halogenfreien thermoplastischen Kunststoff-Rezyklaten sowie stabilisierte Kunststoffzusammensetzungen und hieraus hergestellte Formmassen und Formteile |
| CN113278095A (zh) * | 2021-06-28 | 2021-08-20 | 海南天然橡胶产业集团金橡有限公司 | 一种天然鲜胶乳无氨保存方法 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS492189B1 (de) * | 1970-10-28 | 1974-01-18 | ||
| NZ184467A (en) | 1976-06-28 | 1979-06-08 | Rhone Poulenc Ind | Plasticized stabilized poly(vinyl chloride) |
| SU863602A1 (ru) * | 1979-07-06 | 1981-09-15 | Омский завод синтетического каучука | Композици на основе синтетического латекса |
| JPS6227451A (ja) * | 1985-07-30 | 1987-02-05 | Toyo Soda Mfg Co Ltd | 塩化ビニル系重合体の製造方法 |
| DE3536936A1 (de) * | 1985-10-17 | 1987-04-23 | Huels Chemische Werke Ag | Verfahren zur herstellung von vinylchlorid-polymeren |
| DE3643968A1 (de) | 1986-12-22 | 1988-06-30 | Neynaber Chemie Gmbh | Partialester gesaettigter, geradekettiger c(pfeil abwaerts)2(pfeil abwaerts)(pfeil abwaerts)2(pfeil abwaerts)-c(pfeil abwaerts)3(pfeil abwaerts)(pfeil abwaerts)4(pfeil abwaerts)-monocarbonsaeuren mit polyolen, verfahren zu ihrer herstellung sowie diese enthaltende trennmittel fuer kunststoffe, insbesondere auf basis von pvc oder pvc-copolymerisaten |
| JP2654825B2 (ja) * | 1989-03-28 | 1997-09-17 | 丸善製薬株式会社 | 新規環状イヌロオリゴ糖およびその製造法 |
| DE3919659A1 (de) * | 1989-06-16 | 1990-12-20 | Basf Ag | Verfahren zur herstellung von mit nichtfasrigen kohlehydraten gefuellten ethylen-copolymeren und ihre verwendung |
| AU2802092A (en) | 1991-10-04 | 1993-05-03 | Ferro Corporation, The | Stabilizer systems and products produced utilizing the same |
| DE59409620D1 (de) | 1993-08-10 | 2001-02-01 | Suedzucker Ag | Verwendung von Inulinderivaten |
| TW342404B (en) * | 1994-04-15 | 1998-10-11 | Ciba Sc Holding Ag | Stabilized polyvinyl chloride |
| JPH0948876A (ja) * | 1995-08-04 | 1997-02-18 | Mitsubishi Chem Corp | 熱可塑性樹脂組成物 |
-
1997
- 1997-12-18 DK DK97950504T patent/DK0946634T3/da active
- 1997-12-18 KR KR1019997005504A patent/KR20000069558A/ko not_active Withdrawn
- 1997-12-18 PL PL97334210A patent/PL334210A1/xx unknown
- 1997-12-18 EP EP97950504A patent/EP0946634B1/de not_active Expired - Lifetime
- 1997-12-18 HU HU9903831A patent/HUP9903831A2/hu unknown
- 1997-12-18 US US09/319,997 patent/US6313203B1/en not_active Expired - Fee Related
- 1997-12-18 CA CA002275416A patent/CA2275416A1/en not_active Abandoned
- 1997-12-18 WO PCT/NL1997/000709 patent/WO1998027148A1/en not_active Ceased
- 1997-12-18 SK SK847-99A patent/SK84799A3/sk unknown
- 1997-12-18 DE DE69708323T patent/DE69708323T2/de not_active Expired - Fee Related
- 1997-12-18 AU AU53484/98A patent/AU5348498A/en not_active Abandoned
- 1997-12-18 TR TR1999/01360T patent/TR199901360T2/xx unknown
- 1997-12-18 JP JP52756798A patent/JP2001506301A/ja active Pending
- 1997-12-18 AT AT97950504T patent/ATE208802T1/de not_active IP Right Cessation
- 1997-12-18 CN CN97181334A patent/CN1244880A/zh active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| JP2001506301A (ja) | 2001-05-15 |
| DK0946634T3 (da) | 2002-04-02 |
| AU5348498A (en) | 1998-07-15 |
| KR20000069558A (ko) | 2000-11-25 |
| EP0946634B1 (de) | 2001-11-14 |
| EP0946634A1 (de) | 1999-10-06 |
| TR199901360T2 (xx) | 1999-08-23 |
| WO1998027148A1 (en) | 1998-06-25 |
| ATE208802T1 (de) | 2001-11-15 |
| PL334210A1 (en) | 2000-02-14 |
| CA2275416A1 (en) | 1998-06-25 |
| CN1244880A (zh) | 2000-02-16 |
| DE69708323T2 (de) | 2002-07-11 |
| HUP9903831A2 (hu) | 2000-03-28 |
| US6313203B1 (en) | 2001-11-06 |
| DE69708323D1 (de) | 2001-12-20 |
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