AU561833B2 - Stabilised vinyl chloride polymers - Google Patents

Stabilised vinyl chloride polymers

Info

Publication number
AU561833B2
AU561833B2 AU16517/83A AU1651783A AU561833B2 AU 561833 B2 AU561833 B2 AU 561833B2 AU 16517/83 A AU16517/83 A AU 16517/83A AU 1651783 A AU1651783 A AU 1651783A AU 561833 B2 AU561833 B2 AU 561833B2
Authority
AU
Australia
Prior art keywords
carbon atoms
groups
alkyl
atoms
alkenyl
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
Application number
AU16517/83A
Other versions
AU1651783A (en
Inventor
Louis Carette
Michel Gay
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Rhone Poulenc Specialites Chimiques
Original Assignee
Rhone Poulenc Specialites Chimiques
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.)
Filing date
Publication date
Application filed by Rhone Poulenc Specialites Chimiques filed Critical Rhone Poulenc Specialites Chimiques
Publication of AU1651783A publication Critical patent/AU1651783A/en
Application granted granted Critical
Publication of AU561833B2 publication Critical patent/AU561833B2/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/13Phenols; Phenolates
    • C08K5/138Phenolates
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/0091Complexes with metal-heteroatom-bonds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/09Carboxylic acids; Metal salts thereof; Anhydrides thereof
    • C08K5/098Metal salts of carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/36Sulfur-, selenium-, or tellurium-containing compounds
    • C08K5/37Thiols

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

1. Process for stabilization of polymers based on vinyl chloride characterized by the conjoint use of a) 0.005% to 5% by weight relative to the polymer of at least one organic lanthanide derivative chosen from : lanthanide salts : of monocarboxylic aliphatic acids having from 2 to 30 carbon atoms or dicarboxylic aliphatic acids having from 3 to 30 carbon atoms, the acids being saturated or containing one or more ethylenic double bonds and being able to contain one or more substituents such as halogen atoms, hydroxyl groups, alkoxy groups having from 1 to 12 carbon atoms, mercapto groups or phenyl, phenoxy, naphthyl or cyclohexyl groups in which the rings are optionally substituted with one or more halogen atoms, hydroxyl groups, alkyl groups having 1 to 6 carbon atoms or alkoxy groups having 1 to 6 carbon atoms, ; of benzoic, 1-naphthoic, 2-naphthoic, cyclopentanecarboxylic, cyclohexanecarboxylic, cyclopentenecarboxylic or cyclohexenecarboxylic acids, the cyclic portions of these acids being able to contain one or more substituents such as halogen atoms, hydroxyl groups, alkyl groups having 1 to 12 carbon atoms, alkenyl groups having 2 to 12 carbon atoms, alkoxy groups having 1 to 12 carbon atoms, phenyl, benzyl, phenoxy or cyclohexyl groups, alkoxycarbonyl groups having 2 to 24 carbon atoms or alkenoxycarbonyl groups having 4 to 24 carbon atoms ; of alkyl monoesters (the alkyl group having 1 to 24 carbon atoms) or alkenyl monoesters (the alkenyl group having 3 to 24 carbon atoms) of the dicarboxylic aliphatic acids mentioned above ; of heterocyclic carboxylic acids, in particular those derived from pyridine, furan, thiophene, pyrrole and pyran, which acids can contain one or more substituents such as halogen atoms, hydroxyl groups, alkyl groups having 1 to 12 carbon atoms, alkoxy groups having 1 to 12 carbon atoms, alkenyl groups having 2 to 12 carbon atoms, alkoxycarbonyl groups having 2 to 24 carbon atoms or alkenoxycarbonyl groups having 4 to 24 carbon atoms ; lanthanide phenolates derived from phenol, 1-naphthol or 2-naphthol, in which the cyclic portions can contain one or more substituents such as halogen atoms, alkyl or alkoxy groups having 1 to 24 carbon atoms, alkenyl groups having 2 to 24 carbon atoms, or phenyl, benzyl, phenoxy or cyclohexyl groups ; lanthanide mercaptides, in particular those derived from thioglycolic or thiomalic acid and their alkyl esters (the alkyl radical having 1 to 12 atoms), alkenyl esters (the alkenyl radical having 2 to 12 carbon atoms), phenyl, benzyl and cyclohexyl esters, and esters of alkanediol (having from 2 to 12 carbon atoms), of dihydroxybenzene and of dihydroxycyclohexane, the cyclic portions of the said esters being able to be substituted with one or more alkyl or alkoxy radicals having from 1 to 6 carbon atoms ; lanthanide chelates of beta-dicarbonyl compounds, in particular those derived from the compounds of general formula (I) : R1 -CO-CHR2 -CO-R3 (I) in which : R1 and R3 , which may be identical or different, denote : a linear or branched alkyl group having 1 to 36 carbon atoms and optionally substituted with one or more halogen atoms, a linear or branched alkenyl group having 3 to 36 carbon atoms and optionally substituted with one or more halogen atoms, an aryl radical or an aryl radical bearing one or more substituents on the aromatic ring, such as : . alkyl radicals having 1 to 6 carbon atoms and optionally substituted with one or more halogen atoms, . alkenyl radicals having 2 to 6 carbon atoms and optionally substituted with one or more halogen atoms, . a nitro group, . a -CHO group, . a -COOH group, . alkoxy groups having 1 to 6 carbon atoms, . -COOR4 groups, R4 being an alkyl radical having 1 to 12 carbon atoms or an alkenyl radical having 2 to 12 carbon atoms, . an OH group, . halogen atoms, an aralkyl radical in which the aliphatic portion contains from 1 to 12 carbon atoms and in which the cyclic portion can contain one or more of the substituents mentioned above, a cycloaliphatic radical containing from 5 to 12 carbon atoms and in which the cyclic portion can contain one or more carbon-carbon double bonds and bear one or more of the substituents mentioned above, an arrangement of several of the radicals mentioned above, the different aliphatic radicals defined above being able to contain one or more oxygen -O- or sulphur -S- atoms or carbonyl -CO- or carboxylate -COO- groups ; R2 denotes a hydrogen atom ; b) 0.01% to 1% by weight relative to the polymer of at least one organic zinc or cadmium derivative chosen from : zinc or cadmium salts of the carboxylic acids from which the lanthanide salts mentioned above are derived ; zinc or cadmium phenolates of the phenols from which the lanthanide phenolates mentioned above are derived ; zinc or cadmium mercaptides of thiocarboxylic acids from which the lanthanide mercaptides mentioned above are derived ; c) at least one of the following secondary heat stabilizers : beta-diketones or beta-ketoaldehydes, aminocrotonic acid esters, 2-phenylindole and its derivatives, 1,4-dihydro-2,6-dimethyl-3,5-bis(alkoxycarbonyl)- pyridines, thioglycolic acid esters, thiomalic acid diesters, beta-keto esters, 1,3-dialkyl-6-aminouracils, 1,3-dialkyl-6-amino-2-thiouracils.
AU16517/83A 1982-10-08 1983-07-04 Stabilised vinyl chloride polymers Ceased AU561833B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR8217025A FR2534263B1 (en) 1982-10-08 1982-10-08 PROCESS FOR STABILIZING POLYMERS BASED ON VINYL CHLORIDE
FR8217025 1982-10-08

Publications (2)

Publication Number Publication Date
AU1651783A AU1651783A (en) 1984-04-12
AU561833B2 true AU561833B2 (en) 1987-05-21

Family

ID=9278166

Family Applications (1)

Application Number Title Priority Date Filing Date
AU16517/83A Ceased AU561833B2 (en) 1982-10-08 1983-07-04 Stabilised vinyl chloride polymers

Country Status (7)

Country Link
EP (1) EP0108023B1 (en)
JP (1) JPS5966441A (en)
AT (1) ATE24326T1 (en)
AU (1) AU561833B2 (en)
BR (1) BR8303455A (en)
DE (1) DE3368430D1 (en)
FR (1) FR2534263B1 (en)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2560883B1 (en) * 1984-03-08 1986-10-10 Rhone Poulenc Spec Chim PROCESS FOR THE STABILIZATION OF POLYAMIDES, THE STABILIZING COMPOSITIONS USED FOR THE IMPLEMENTATION OF THIS PROCESS AND THE STABILIZED POLYAMIDES OBTAINED
EP0294126A3 (en) * 1987-06-01 1990-08-01 Ferro Corporation Halogen-containing resin composition
DE4116812A1 (en) * 1991-05-23 1992-11-26 Rehau Ag & Co MEDICAL TOOLS
US5322872A (en) * 1993-04-14 1994-06-21 The Lubrizol Corporation Stabilized compositions of mixed metal carboxylates
US5332772A (en) * 1993-05-05 1994-07-26 Morton International, Inc. Combination heat stabilizer/lubricant for PVC processing and method for producing the same
DK0930332T3 (en) * 1998-01-16 2003-07-21 Crompton Vinyl Additives Gmbh Stabilizer system for chlorine-containing polymers
DK0962491T3 (en) 1998-06-02 2003-08-11 Crompton Vinyl Additives Gmbh Cyanacetylureas for stabilizing halogen-containing polymers
DK0967209T3 (en) 1998-06-26 2003-03-24 Crompton Vinyl Additives Gmbh Novel NH2-modified 6-aminouracils as stabilizers of halogen-containing polymers
EP1510545A3 (en) 1998-06-26 2005-06-15 Wolfgang Dr. Wehner 1,3 substituted 6-aminouraciles to stabilize halogenated polymers
FR2869618B1 (en) * 2004-04-30 2008-10-10 Michelin Soc Tech IMPROVED ADHESIVE RUBBER COMPOSITION WITH A METAL REINFORCEMENT.
CN100457810C (en) * 2006-12-31 2009-02-04 中国科学院广州化学研究所 Orgnic rare earth thiolate composite stabilizator for halogen-containing polymer and application thereof
CN100509778C (en) * 2006-12-31 2009-07-08 中国科学院广州化学研究所 Rare earth thiolate derivate and preparation process thereof
EP2123659A1 (en) 2008-05-15 2009-11-25 Arkema France High purity monoalkyltin compounds and uses thereof

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4102839A (en) * 1975-01-10 1978-07-25 Rhone-Poulenc Industries Stabilization of vinyl chloride polymers

Also Published As

Publication number Publication date
ATE24326T1 (en) 1987-01-15
JPS5966441A (en) 1984-04-14
DE3368430D1 (en) 1987-01-29
BR8303455A (en) 1984-06-12
AU1651783A (en) 1984-04-12
EP0108023A1 (en) 1984-05-09
FR2534263B1 (en) 1986-09-19
EP0108023B1 (en) 1986-12-17
FR2534263A1 (en) 1984-04-13

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