NO780966L - Smoeremiddel for polyvinylkloridplast - Google Patents

Smoeremiddel for polyvinylkloridplast

Info

Publication number: NO780966L
Authority: NO; Norway
Prior art keywords: vinyl chloride; additive according; chloride polymer; hydroxide; additive
Prior art date: 1977-04-06

Application number

NO780966A

Other languages

English (en)

Norwegian (no)

Inventor

Adam Joseph Ejk

Original Assignee

M & T Chemicals Inc

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1977-04-06

Filing date

1978-03-17

Publication date

1978-10-09

1978-03-17 Application filed by M & T Chemicals Inc filed Critical M & T Chemicals Inc

1978-10-09 Publication of NO780966L publication Critical patent/NO780966L/no

Links

239000000314 lubricant Substances 0.000 title claims description 37
239000004800 polyvinyl chloride Substances 0.000 title description 6
229920000915 polyvinyl chloride Polymers 0.000 title description 6
229920003023 plastic Polymers 0.000 title description 2
239000004033 plastic Substances 0.000 title description 2
239000000203 mixture Substances 0.000 claims description 46
229920000642 polymer Polymers 0.000 claims description 46
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 35
239000002253 acid Substances 0.000 claims description 19
239000000654 additive Substances 0.000 claims description 18
230000000996 additive effect Effects 0.000 claims description 16
150000002148 esters Chemical class 0.000 claims description 14
125000004432 carbon atom Chemical group C* 0.000 claims description 13
150000001875 compounds Chemical class 0.000 claims description 13
239000012760 heat stabilizer Substances 0.000 claims description 13
-1 polyethylene Polymers 0.000 claims description 13
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 11
239000004698 Polyethylene Substances 0.000 claims description 10
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical group O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 10
150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 10
229920000573 polyethylene Polymers 0.000 claims description 10
239000001993 wax Substances 0.000 claims description 10
239000012188 paraffin wax Substances 0.000 claims description 9
AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 claims description 8
239000000920 calcium hydroxide Substances 0.000 claims description 8
229910001861 calcium hydroxide Inorganic materials 0.000 claims description 8
229920001577 copolymer Polymers 0.000 claims description 8
239000000463 material Substances 0.000 claims description 7
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 6
125000004185 ester group Chemical group 0.000 claims description 6
229920001519 homopolymer Polymers 0.000 claims description 6
239000005977 Ethylene Substances 0.000 claims description 5
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 5
150000001735 carboxylic acids Chemical class 0.000 claims description 5
238000006243 chemical reaction Methods 0.000 claims description 5
239000004408 titanium dioxide Substances 0.000 claims description 5
150000001336 alkenes Chemical class 0.000 claims description 4
229910052787 antimony Inorganic materials 0.000 claims description 4
WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims description 4
ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 claims description 4
150000004679 hydroxides Chemical class 0.000 claims description 4
229910052751 metal Inorganic materials 0.000 claims description 4
150000002763 monocarboxylic acids Chemical class 0.000 claims description 4
150000001298 alcohols Chemical class 0.000 claims description 3
229910052784 alkaline earth metal Inorganic materials 0.000 claims description 3
239000000049 pigment Substances 0.000 claims description 3
IVORCBKUUYGUOL-UHFFFAOYSA-N 1-ethynyl-2,4-dimethoxybenzene Chemical compound COC1=CC=C(C#C)C(OC)=C1 IVORCBKUUYGUOL-UHFFFAOYSA-N 0.000 claims description 2
125000000217 alkyl group Chemical group 0.000 claims description 2
WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims description 2
RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 claims description 2
229910001863 barium hydroxide Inorganic materials 0.000 claims description 2
BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 claims description 2
239000000292 calcium oxide Substances 0.000 claims description 2
ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims description 2
UUCCCPNEFXQJEL-UHFFFAOYSA-L strontium dihydroxide Chemical compound [OH-].[OH-].[Sr+2] UUCCCPNEFXQJEL-UHFFFAOYSA-L 0.000 claims description 2
229910001866 strontium hydroxide Inorganic materials 0.000 claims description 2
239000000945 filler Substances 0.000 claims 1
239000000395 magnesium oxide Substances 0.000 claims 1
CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims 1
AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims 1
229920006395 saturated elastomer Polymers 0.000 claims 1
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 8
239000000155 melt Substances 0.000 description 7
229910000000 metal hydroxide Inorganic materials 0.000 description 7
229910044991 metal oxide Inorganic materials 0.000 description 7
150000004706 metal oxides Chemical class 0.000 description 7
235000021355 Stearic acid Nutrition 0.000 description 5
235000014113 dietary fatty acids Nutrition 0.000 description 5
239000000194 fatty acid Substances 0.000 description 5
229930195729 fatty acid Natural products 0.000 description 5
150000004665 fatty acids Chemical class 0.000 description 5
238000002844 melting Methods 0.000 description 5
230000008018 melting Effects 0.000 description 5
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 5
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 5
238000012545 processing Methods 0.000 description 5
150000003839 salts Chemical class 0.000 description 5
239000008117 stearic acid Substances 0.000 description 5
229910052717 sulfur Inorganic materials 0.000 description 5
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
229910000019 calcium carbonate Inorganic materials 0.000 description 4
238000002845 discoloration Methods 0.000 description 4
230000000694 effects Effects 0.000 description 4
238000013112 stability test Methods 0.000 description 4
239000003381 stabilizer Substances 0.000 description 4
RZBBHEJLECUBJT-UHFFFAOYSA-N 6-methylheptyl 2-sulfanylacetate Chemical compound CC(C)CCCCCOC(=O)CS RZBBHEJLECUBJT-UHFFFAOYSA-N 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
230000015556 catabolic process Effects 0.000 description 3
238000000034 method Methods 0.000 description 3
230000000737 periodic effect Effects 0.000 description 3
238000007127 saponification reaction Methods 0.000 description 3
230000002195 synergetic effect Effects 0.000 description 3
VNPRJHMMOKDEDZ-UHFFFAOYSA-L 6-methylheptyl 2-[dibutyl-[2-(6-methylheptoxy)-2-oxoethyl]sulfanylstannyl]sulfanylacetate Chemical compound CC(C)CCCCCOC(=O)CS[Sn](CCCC)(CCCC)SCC(=O)OCCCCCC(C)C VNPRJHMMOKDEDZ-UHFFFAOYSA-L 0.000 description 2
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 2
239000008116 calcium stearate Substances 0.000 description 2
235000013539 calcium stearate Nutrition 0.000 description 2
125000002843 carboxylic acid group Chemical group 0.000 description 2
239000003086 colorant Substances 0.000 description 2
238000006731 degradation reaction Methods 0.000 description 2
238000010586 diagram Methods 0.000 description 2
150000001991 dicarboxylic acids Chemical class 0.000 description 2
238000011156 evaluation Methods 0.000 description 2
229910000464 lead oxide Inorganic materials 0.000 description 2
230000007774 longterm Effects 0.000 description 2
239000002184 metal Substances 0.000 description 2
230000003647 oxidation Effects 0.000 description 2
238000007254 oxidation reaction Methods 0.000 description 2
YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 description 2
230000006641 stabilisation Effects 0.000 description 2
238000011105 stabilization Methods 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000011593 sulfur Substances 0.000 description 2
229910052725 zinc Inorganic materials 0.000 description 2
239000011701 zinc Substances 0.000 description 2
239000011787 zinc oxide Substances 0.000 description 2
SHGAZHPCJJPHSC-WBBXYVSWSA-N (2e,4e,6e,8z)-3,7-dimethyl-9-(2,6,6-trimethylcyclohexen-1-yl)nona-2,4,6,8-tetraenoic acid Chemical compound OC(=O)\C=C(/C)\C=C\C=C(/C)\C=C/C1=C(C)CCCC1(C)C SHGAZHPCJJPHSC-WBBXYVSWSA-N 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
230000002411 adverse Effects 0.000 description 1
150000001342 alkaline earth metals Chemical class 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
150000007514 bases Chemical class 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229910052793 cadmium Inorganic materials 0.000 description 1
BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
229940065285 cadmium compound Drugs 0.000 description 1
150000001662 cadmium compounds Chemical class 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000011575 calcium Substances 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
239000000470 constituent Substances 0.000 description 1
238000007334 copolymerization reaction Methods 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
239000000539 dimer Substances 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
239000012530 fluid Substances 0.000 description 1
235000013305 food Nutrition 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
XCAUINMIESBTBL-UHFFFAOYSA-N lead(ii) sulfide Chemical compound [Pb]=S XCAUINMIESBTBL-UHFFFAOYSA-N 0.000 description 1
230000001050 lubricating effect Effects 0.000 description 1
238000005461 lubrication Methods 0.000 description 1
150000002736 metal compounds Chemical class 0.000 description 1
150000004692 metal hydroxides Chemical class 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
125000005395 methacrylic acid group Chemical class 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
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 1
239000004209 oxidized polyethylene wax Substances 0.000 description 1
235000013873 oxidized polyethylene wax Nutrition 0.000 description 1
PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
239000011505 plaster Substances 0.000 description 1
238000012667 polymer degradation Methods 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
230000002028 premature Effects 0.000 description 1
238000010186 staining Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000012360 testing method Methods 0.000 description 1
238000012546 transfer Methods 0.000 description 1
239000013638 trimer Substances 0.000 description 1
238000011144 upstream manufacturing Methods 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
150000003752 zinc compounds Chemical class 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- 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
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/26—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment
- C08L23/30—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment by oxidation
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of 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; Compositions of derivatives of such polymers
- C08L27/02—Compositions of 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; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/04—Compositions of 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; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C08L27/06—Homopolymers or copolymers of vinyl chloride
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L91/00—Compositions of oils, fats or waxes; Compositions of derivatives thereof
- C08L91/06—Waxes

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
General Chemical & Material Sciences (AREA)
Compositions Of Macromolecular Compounds (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

NO780966A 1977-04-06 1978-03-17 Smoeremiddel for polyvinylkloridplast NO780966L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US05/784,961 US4132691A (en)	1977-04-06	1977-04-06	Lubricant composition for vinyl chloride polymers

Publications (1)

Publication Number	Publication Date
NO780966L true NO780966L (no)	1978-10-09

Family

ID=25134060

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO780966A NO780966L (no)	1977-04-06	1978-03-17	Smoeremiddel for polyvinylkloridplast

Country Status (18)

Country	Link
US (1)	US4132691A (fr)
JP (1)	JPS53126052A (fr)
AU (1)	AU517286B2 (fr)
BE (1)	BE865600A (fr)
BR (1)	BR7802078A (fr)
CA (1)	CA1093808A (fr)
CS (1)	CS203190B2 (fr)
DE (1)	DE2814925C2 (fr)
DK (1)	DK148978A (fr)
ES (1)	ES468559A1 (fr)
FR (1)	FR2386578B1 (fr)
GB (1)	GB1573697A (fr)
IT (1)	IT1203140B (fr)
NL (1)	NL7803680A (fr)
NO (1)	NO780966L (fr)
NZ (1)	NZ186853A (fr)
PL (1)	PL112191B1 (fr)
SE (1)	SE7803845L (fr)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4203880B1 (en) *	1978-11-13	1994-04-26	M & T Chemicals Inc	Lubricant composition for halogen-containing polymers
US4248747A (en) *	1979-08-03	1981-02-03	Conoco, Inc.	Single package additive for thermoplastic formulation
US4246150A (en) *	1979-09-17	1981-01-20	American Hoechst Corporation	Lubricant for heat processing of vinyl chloride resins
GB2075989B (en) *	1980-05-13	1984-04-26	Kyowa Chem Ind Co Ltd	Stabilized thermoplastic resin compositions
US4358555A (en) *	1981-06-02	1982-11-09	Carstab Corporation	Stabilizers for halogen containing polymers comprising alkyltin compounds, zinc mercaptoesters and basic alkali or alkaline earth metal compounds
JPS58123598U (ja) *	1982-02-16	1983-08-23	松下電器産業株式会社	高周波加熱装置
US4515916A (en) *	1982-05-18	1985-05-07	Morton Thiokol Inc.	Stabilizers for halogen containing polymers comprising zinc mercaptoesters, basic inorganic alkali or alkaline earth metal compounds and, substituted dihydropyridines
JPS6363738A (ja) *	1986-09-05	1988-03-22	Toyo Seikan Kaisha Ltd	熱成形性塩化ビニリデン樹脂組成物
EP0388424A4 (en) *	1987-10-09	1991-03-13	The Dow Chemical Company	Vinylidene chloride interpolymer
CA1329288C (fr) *	1987-10-09	1994-05-03	Mark J. Hall	Interpolymere de chlorure de vinylidene
DE68927346T2 (de) *	1988-03-07	1997-05-07	Dow Chemical Co	Formulierungspaket zur extrusion von vinylidenchloridinterpolymerisaten und dieses paket enthaltende polyvinylidenchloridzusammensetzung
US4965304A (en) *	1988-07-05	1990-10-23	The Dow Chemical Company	Extrudable polymeric compositions
PT91654B (pt) *	1988-09-08	1995-05-31	Shinetsu Chemical Co	Processo de preparacao de resina a base de cloreto de vinilo
US5002989A (en) *	1989-09-01	1991-03-26	The Dow Chemical Company	Formulation for extrudable vinylidene chloride copolymers having high barrier properties
US5087669A (en) *	1989-09-18	1992-02-11	The Dow Chemical Company	Vinyl chloride polymer composition with improved fusion properties
EP0642548B1 (fr) *	1992-05-19	1998-07-01	Witco Corporation	Composition a base de resine de chlorure de polyvinyle a qualite electrique et stabilisee au moyen d'un stabilisant sans plomb
JPH09501462A (ja) *	1993-08-11	1997-02-10	アライドシグナル・インコーポレーテッド	硬質ビニル重合体のための外部潤滑剤組成物
US5426144A (en) *	1993-08-11	1995-06-20	Alliedsignal Inc.	External lubricant and stabilizer compositions for rigid vinyl polymers
US5414035A (en) *	1994-07-01	1995-05-09	Alliedsignal Inc.	Calendered rigid vinyl polymer compositions
US5777014A (en) *	1996-12-03	1998-07-07	The C.P. Hall Company	PVC sheet material having improved water-based coating receptivity
DE19860174A1 (de) *	1998-12-24	2000-06-29	Clariant Gmbh	Polymeroxidate und ihre Verwendung
DE19914798A1 (de) *	1999-03-31	2000-10-05	Baerlocher Gmbh	Stabilisatorkombination für halogenhaltige thermoplastische Harzzusammensetzungen
WO2004083301A1 (fr) *	2003-03-14	2004-09-30	Honeywell International, Inc.	Compositions de resine renforcee de cellulose
DE102004024272A1 (de) *	2004-05-15	2005-12-01	Lanxess Deutschland Gmbh	Pfropfpolymerisathaltige Massen für die Extrusionsverarbeitung
DE102005049404A1 (de) *	2005-10-13	2007-04-26	Basf Ag	Verfahren zur Verarbeitung von Hart-Polyvinylchlorid
US7709571B2 (en) *	2006-10-30	2010-05-04	Honeywell International Inc	Multicomponent lubricant composition for processing rigid vinyl chloride polymers
US8664314B2 (en) *	2007-02-23	2014-03-04	Basf Se	Mixtures of N-alkanols and their use

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3172801A (en) *		1965-03-09		Heat-sealable waxed packaging mate- rial and process of making the same
US2855266A (en) *	1953-02-16	1958-10-07	Little Inc A	Heat sensitive materials for recording instruments
DE1694140A1 (de) *	1967-03-25	1971-07-22	Hoechst Ag	Gleitmittel fuer die Verarbeitung von Polyvinylchlorid
US3757001A (en) *	1971-04-16	1973-09-04	Allied Chem	Method for suspension polymerization of vinyl chloride
CS156663B1 (fr) *	1971-10-07	1974-08-23
DE2201863A1 (de) *	1972-01-15	1973-07-19	Hoechst Ag	Gleitmittel fuer pvc
US3760036A (en) *	1972-04-12	1973-09-18	Reynolds Metals Co	Pva lubricant for polyvinyl chloride
FR2217363B1 (fr) *	1972-06-26	1977-05-06	Solvay
JPS5087441A (fr) *	1973-12-10	1975-07-14
JPS5141787A (ja) *	1974-10-07	1976-04-08	Mitsui Petrochemical Ind	Sankahoriechirenwatsukusukinzokuenno seizohoho
JPS5141747A (en) *	1974-10-07	1976-04-08	Mitsui Petrochemical Ind	Katsusei tomeiseiganensojushisoseibutsu

1977
- 1977-04-06 US US05/784,961 patent/US4132691A/en not_active Expired - Lifetime
1978
- 1978-03-17 NO NO780966A patent/NO780966L/no unknown
- 1978-03-22 GB GB11438/78A patent/GB1573697A/en not_active Expired
- 1978-03-29 FR FR7809149A patent/FR2386578B1/fr not_active Expired
- 1978-03-31 BE BE186497A patent/BE865600A/fr not_active IP Right Cessation
- 1978-04-03 NZ NZ186853A patent/NZ186853A/xx unknown
- 1978-04-04 DK DK148978A patent/DK148978A/da not_active IP Right Cessation
- 1978-04-04 AU AU34754/78A patent/AU517286B2/en not_active Expired
- 1978-04-04 BR BR7802078A patent/BR7802078A/pt unknown
- 1978-04-05 SE SE7803845A patent/SE7803845L/xx unknown
- 1978-04-05 CA CA300,504A patent/CA1093808A/fr not_active Expired
- 1978-04-05 PL PL1978205820A patent/PL112191B1/pl unknown
- 1978-04-05 ES ES468559A patent/ES468559A1/es not_active Expired
- 1978-04-05 CS CS782225A patent/CS203190B2/cs unknown
- 1978-04-05 IT IT09409/78A patent/IT1203140B/it active
- 1978-04-06 JP JP3982778A patent/JPS53126052A/ja active Pending
- 1978-04-06 DE DE2814925A patent/DE2814925C2/de not_active Expired
- 1978-04-06 NL NL7803680A patent/NL7803680A/xx not_active Application Discontinuation

Also Published As

Publication number	Publication date
CA1093808A (fr)	1981-01-20
IT1203140B (it)	1989-02-15
DE2814925C2 (de)	1986-08-28
AU3475478A (en)	1979-10-11
PL112191B1 (en)	1980-09-30
DE2814925A1 (de)	1978-10-12
JPS53126052A (en)	1978-11-02
US4132691A (en)	1979-01-02
DK148978A (da)	1978-10-07
AU517286B2 (en)	1981-07-23
NL7803680A (nl)	1978-10-10
BE865600A (fr)	1978-07-17
NZ186853A (en)	1980-04-28
BR7802078A (pt)	1978-11-28
CS203190B2 (en)	1981-02-27
PL205820A1 (pl)	1979-01-29
FR2386578B1 (fr)	1985-06-21
IT7809409A0 (it)	1978-04-05
GB1573697A (en)	1980-08-28
ES468559A1 (es)	1978-11-16
SE7803845L (sv)	1978-10-07
FR2386578A1 (fr)	1978-11-03

Publication	Publication Date	Title
NO780966L (no)	1978-10-09	Smoeremiddel for polyvinylkloridplast
US4192930A (en)	1980-03-11	Esterified olefin-maleic anhydride copolymers
US3867481A (en)	1975-02-18	Low molecular weight acrylic modifiers for rigid vinyl halide polymers
NO793339L (no)	1980-05-14	Halogenholdig plast og sammensetning til bruk i plasten
CA2054908A1 (fr)	1992-06-28	Compositions polymeriques contenant un halogene stabilise
MXPA06013116A (es)	2007-02-28	Agentes de recubrimiento desprovistos de conservadores, metodo para su produccion y uso.
US4267084A (en)	1981-05-12	Vinyl chloride polymer blend composition
US3741909A (en)	1973-06-26	Antioxidant composition to stabilize organic materials
US3642635A (en)	1972-02-15	Synthetic petrolatum compositions
US3322708A (en)	1967-05-30	Polypropylene compositions
EP0065569B1 (fr)	1986-05-28	Compositions de copolymeres de chlorure de vinylidene d'extrusion et films prepares a partir de ces compositions
CN111876019B (zh)	2022-06-24	一种水性光油及制备工艺
US2479918A (en)	1949-08-23	Stabilized vinyl chloride resins
US4139522A (en)	1979-02-13	Stabilized ethylene-carbon monoxide copolymers
KR810001539B1 (ko)	1981-10-27	경질 염화비닐 중합체용 개량첨가제
JP3224753B2 (ja)	2001-11-05	Ｐｖｃ加工用熱安定剤／潤滑剤およびその製造法
MXPA99006431A (es)	2003-07-21	Composicion a base de maleatos de organoestanoutil para estabilizar y lubricar polimerostermoplasticos y metodo para la obtencion de dichacomposicion.
NO171794B (no)	1993-01-25	Vulkaniserbart nitrilgummimateriale
NO801260L (no)	1980-11-05	Fremgangsmaate for varmestabilisering av plastmaterialer
US3626031A (en)	1971-12-07	Vinyl halide polymer stabilized with partial ester salt of maleic anhydride-vinyl compound polymer
US4843117A (en)	1989-06-27	Dimethyl sulfone as a solid solvent for vinylidene chloride containing polymers
US4696754A (en)	1987-09-29	Lubricant-stabilizer compositions for halogen-containing organic polymers and polymer compositions thereof
US2855417A (en)	1958-10-07	Organotin compounds and process of preparation
CN115584096B (zh)	2023-12-29	一种氯化聚氯乙烯组合物及其制备方法与应用
US3246963A (en)	1966-04-19	Compositions containing wax and either a wax-naphthalene condensation product or certain fumarate ester containing polymers