SE414407B - Stabiliserad vinylkloridpolymerkomposition och medel for stabiliseringen - Google Patents
Stabiliserad vinylkloridpolymerkomposition och medel for stabiliseringenInfo
- Publication number
- SE414407B SE414407B SE6907332A SE733269A SE414407B SE 414407 B SE414407 B SE 414407B SE 6907332 A SE6907332 A SE 6907332A SE 733269 A SE733269 A SE 733269A SE 414407 B SE414407 B SE 414407B
- Authority
- SE
- Sweden
- Prior art keywords
- stabilizer
- parts
- vinyl chloride
- weight
- denotes
- Prior art date
Links
- 229920000642 polymer Polymers 0.000 title claims description 30
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 title claims description 27
- 239000000203 mixture Substances 0.000 title claims description 26
- 230000006641 stabilisation Effects 0.000 title description 3
- 238000011105 stabilization Methods 0.000 title description 3
- 239000003381 stabilizer Substances 0.000 claims description 54
- 125000000217 alkyl group Chemical group 0.000 claims description 10
- YSCDKUPSJMMGGT-UHFFFAOYSA-L [dibutyl-[2-(6-methylheptylsulfanyl)acetyl]oxystannyl] 2-(6-methylheptylsulfanyl)acetate Chemical group CC(C)CCCCCSCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CSCCCCCC(C)C YSCDKUPSJMMGGT-UHFFFAOYSA-L 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- DTYWIPLKZHQUMW-UHFFFAOYSA-N dibutyl(diphenyl)stannane Chemical group C=1C=CC=CC=1[Sn](CCCC)(CCCC)C1=CC=CC=C1 DTYWIPLKZHQUMW-UHFFFAOYSA-N 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 6
- 230000000087 stabilizing effect Effects 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- RZBBHEJLECUBJT-UHFFFAOYSA-N 6-methylheptyl 2-sulfanylacetate Chemical compound CC(C)CCCCCOC(=O)CS RZBBHEJLECUBJT-UHFFFAOYSA-N 0.000 claims description 4
- 230000001066 destructive effect Effects 0.000 claims description 3
- AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical group CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 claims description 2
- PIILXFBHQILWPS-UHFFFAOYSA-N tributyltin Chemical compound CCCC[Sn](CCCC)CCCC PIILXFBHQILWPS-UHFFFAOYSA-N 0.000 claims 2
- 238000005096 rolling process Methods 0.000 description 13
- 239000011347 resin Substances 0.000 description 11
- 229920005989 resin Polymers 0.000 description 11
- -1 for example Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 5
- 229910052736 halogen Inorganic materials 0.000 description 4
- 150000002367 halogens Chemical class 0.000 description 4
- 239000000314 lubricant Substances 0.000 description 4
- 239000000945 filler Substances 0.000 description 3
- 229920001519 homopolymer Polymers 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 238000013112 stability test Methods 0.000 description 3
- LVMCAEWDDHHMDZ-UHFFFAOYSA-K [butyl-di(octanoyloxy)stannyl] octanoate Chemical compound CCCC[Sn+3].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O.CCCCCCCC([O-])=O LVMCAEWDDHHMDZ-UHFFFAOYSA-K 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 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 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000011342 resin composition Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- YPAJTRDCBQWRFW-UHFFFAOYSA-L 2-cyclohexyl-2-sulfanylacetate;dibutyltin(2+) Chemical compound CCCC[Sn+2]CCCC.[O-]C(=O)C(S)C1CCCCC1.[O-]C(=O)C(S)C1CCCCC1 YPAJTRDCBQWRFW-UHFFFAOYSA-L 0.000 description 1
- MUWBADGLKHMCGP-UHFFFAOYSA-N 4,4,4-triphenylbutyltin Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(CCC[Sn])C1=CC=CC=C1 MUWBADGLKHMCGP-UHFFFAOYSA-N 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 229920006385 Geon Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- FKXJWELJXMKBDI-UHFFFAOYSA-K [butyl-di(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(OC(=O)CCCCCCCCCCC)OC(=O)CCCCCCCCCCC FKXJWELJXMKBDI-UHFFFAOYSA-K 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 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 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 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
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 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 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- JJPZOIJCDNHCJP-UHFFFAOYSA-N dibutyl(sulfanylidene)tin Chemical compound CCCC[Sn](=S)CCCC JJPZOIJCDNHCJP-UHFFFAOYSA-N 0.000 description 1
- PXQGTURWBNIMIM-UHFFFAOYSA-N dicyclohexyl(diphenyl)stannane Chemical compound C1CCCCC1[Sn](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1CCCCC1 PXQGTURWBNIMIM-UHFFFAOYSA-N 0.000 description 1
- DEBGIHHGDBIVJW-UHFFFAOYSA-L dicyclohexyltin(2+);2-(6-methylheptylsulfanyl)acetate Chemical compound CC(C)CCCCCSCC([O-])=O.CC(C)CCCCCSCC([O-])=O.C1CCCCC1[Sn+2]C1CCCCC1 DEBGIHHGDBIVJW-UHFFFAOYSA-L 0.000 description 1
- INCQQSKGFIBXAY-UHFFFAOYSA-N dimethyl(diphenyl)stannane Chemical compound C=1C=CC=CC=1[Sn](C)(C)C1=CC=CC=C1 INCQQSKGFIBXAY-UHFFFAOYSA-N 0.000 description 1
- VXGIVDFKZKMKQO-UHFFFAOYSA-L dioctyltin isooctylthioglycolate Chemical compound CCCCC(CC)COC(=O)CS[Sn](CCCCCCCC)(CCCCCCCC)SCC(=O)OCC(CC)CCCC VXGIVDFKZKMKQO-UHFFFAOYSA-L 0.000 description 1
- QWXSPIOOSOTTAU-UHFFFAOYSA-L dodecyl 2-[dibutyl-(2-dodecoxy-2-oxoethyl)sulfanylstannyl]sulfanylacetate Chemical compound CCCCCCCCCCCCOC(=O)CS[Sn](CCCC)(CCCC)SCC(=O)OCCCCCCCCCCCC QWXSPIOOSOTTAU-UHFFFAOYSA-L 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 229920005570 flexible polymer Polymers 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 238000005098 hot rolling Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 239000000178 monomer Substances 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
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical compound CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 description 1
- RMCGDGIGQJQINH-UHFFFAOYSA-N octyl(triphenyl)stannane Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(CCCCCCCC)C1=CC=CC=C1 RMCGDGIGQJQINH-UHFFFAOYSA-N 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- AFCAKJKUYFLYFK-UHFFFAOYSA-N tetrabutyltin Chemical compound CCCC[Sn](CCCC)(CCCC)CCCC AFCAKJKUYFLYFK-UHFFFAOYSA-N 0.000 description 1
- CWERGRDVMFNCDR-UHFFFAOYSA-M thioglycolate(1-) Chemical compound [O-]C(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-M 0.000 description 1
- 238000004383 yellowing Methods 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
- C08K5/56—Organo-metallic compounds, i.e. organic compounds containing a metal-to-carbon bond
- C08K5/57—Organo-tin compounds
- C08K5/58—Organo-tin compounds containing sulfur
-
- 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
- C08K5/56—Organo-metallic compounds, i.e. organic compounds containing a metal-to-carbon bond
- C08K5/57—Organo-tin compounds
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)
- Polyethers (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US73202768A | 1968-05-27 | 1968-05-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SE414407B true SE414407B (sv) | 1980-07-28 |
Family
ID=24941891
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE6907332A SE414407B (sv) | 1968-05-27 | 1969-05-23 | Stabiliserad vinylkloridpolymerkomposition och medel for stabiliseringen |
| SE7511933A SE435848B (sv) | 1968-05-27 | 1975-10-24 | Vinylkloridpolymerkomposition, som er stabiliserad gentemot den forstorande verkan av verme och medel for stabiliseringen |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE7511933A SE435848B (sv) | 1968-05-27 | 1975-10-24 | Vinylkloridpolymerkomposition, som er stabiliserad gentemot den forstorande verkan av verme och medel for stabiliseringen |
Country Status (8)
| Country | Link |
|---|---|
| AT (1) | AT307054B (enrdf_load_stackoverflow) |
| BE (1) | BE733579A (enrdf_load_stackoverflow) |
| CH (1) | CH525918A (enrdf_load_stackoverflow) |
| DE (1) | DE1926949B2 (enrdf_load_stackoverflow) |
| ES (1) | ES367675A1 (enrdf_load_stackoverflow) |
| FR (1) | FR2009375A1 (enrdf_load_stackoverflow) |
| NL (1) | NL159420B (enrdf_load_stackoverflow) |
| SE (2) | SE414407B (enrdf_load_stackoverflow) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3067234D1 (en) * | 1979-02-22 | 1984-05-03 | Ciba Geigy Ag | Mixtures consisting of an organo-tin alcoholate and an organo-tin mercaptide; their use as stabilizers for chlorinated polymers |
| US4988750A (en) * | 1981-07-17 | 1991-01-29 | Schering Ag | Non-toxic stabilizer for halogenated polymer |
-
1969
- 1969-05-21 NL NL6907753.A patent/NL159420B/xx not_active IP Right Cessation
- 1969-05-22 FR FR6916726A patent/FR2009375A1/fr active Pending
- 1969-05-23 SE SE6907332A patent/SE414407B/sv unknown
- 1969-05-23 BE BE733579D patent/BE733579A/xx not_active IP Right Cessation
- 1969-05-25 ES ES367675A patent/ES367675A1/es not_active Expired
- 1969-05-27 CH CH802869A patent/CH525918A/de not_active IP Right Cessation
- 1969-05-27 DE DE1926949A patent/DE1926949B2/de not_active Ceased
- 1969-05-27 AT AT502869A patent/AT307054B/de not_active IP Right Cessation
-
1975
- 1975-10-24 SE SE7511933A patent/SE435848B/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| ES367675A1 (es) | 1971-04-16 |
| DE1926949B2 (de) | 1981-02-05 |
| BE733579A (enrdf_load_stackoverflow) | 1969-11-03 |
| CH525918A (de) | 1972-07-31 |
| AT307054B (de) | 1973-05-10 |
| SE435848B (sv) | 1984-10-22 |
| NL159420B (nl) | |
| NL6907753A (enrdf_load_stackoverflow) | 1969-12-01 |
| FR2009375A1 (en) | 1970-02-06 |
| DE1926949A1 (de) | 1970-04-16 |
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