ES268116A1 - Polyvinyl chloride stabiliser combinations and polyvinyl chloride resins stabilised thereby - Google Patents

Polyvinyl chloride stabiliser combinations and polyvinyl chloride resins stabilised thereby

Info

Publication number
ES268116A1
ES268116A1 ES0268116A ES268116A ES268116A1 ES 268116 A1 ES268116 A1 ES 268116A1 ES 0268116 A ES0268116 A ES 0268116A ES 268116 A ES268116 A ES 268116A ES 268116 A1 ES268116 A1 ES 268116A1
Authority
ES
Spain
Prior art keywords
carbon atoms
polyvinyl chloride
cadmium
resins
phenol
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.)
Expired
Application number
ES0268116A
Other languages
Spanish (es)
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.)
Argus Chemical Corp
Original Assignee
Argus Chemical Corp
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 Argus Chemical Corp filed Critical Argus Chemical Corp
Publication of ES268116A1 publication Critical patent/ES268116A1/en
Expired 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
    • C08K5/09Carboxylic 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
    • C08K5/0008Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
    • C08K5/005Stabilisers against oxidation, heat, light, ozone
    • 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
    • C08K5/05Alcohols; Metal alcoholates
    • C08K5/053Polyhydroxylic alcohols
    • 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

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)

Abstract

Polyvinyl chloride resins are stabilized with a composition comprising (1) a polyol <FORM:0934644/IV(a)/1> where R is hydrogen or an alkyl or alkoxy group the alkyl or alkoxy group may include additional substituents, e.g. hydroxyl or alkoxy groups or both together and the R radical, when not hydrogen, has from 1 to 30 carbon atoms, (2) a hydrocarbon-substituted phenol having at least one phenolic hydroxyl group and from 1 to 30 carbon atoms per phenolic hydroxyl group and (3) a metal salt stabilizer which is a salt of a polyvalent metal and an organic monocarboxylic acid having from 6 to 18 carbon atoms and which contains no nitrogen atoms. Typical polyols include dipentaerythritol, trimethylolpropane, trimethylolethane and trimethylolbutane. The phenol contains one or more phenolic hydroxyl groups and may contain one or more phenolic nuclei and the phenolic nucleus may have an oxy or thioether substituent. In addition the phenol will have one or a plurality of alkyl, aryl or cycloalkyl substituents or a second ring condensed therewith as in the naphthols, having one or more carbon atoms, up to the total number of carbon atoms per phenolic hydroxyl group. The phenols may have from one to five substituent radicals per phenolic nucleus. Lists of suitable phenols are given. The acid component of the metal salt stabilizer may be aliphatic, aromatic, alicyclic or heterocyclic monocarboxylic acids having oxygen in the heterocyclic ring. The acids may be substituted with halogen, sulphur and hydroxyl groups and the metal component is preferably an alkaline earth metal e.g. magnesium, barium, strontium, calcium, or zinc, cadmium, lead or tin. Lists of acids are given. The stabilizer composition of the invention may have in addition other stabilizers normally used with polyvinyl chloride resins. Epoxy compounds having from 10 to 150 carbon atoms may also be added. A plasticizer, e.g. dioctyl phthalate, dioctyl sebacate, tricresyl phosphate and epoxy higher esters having from 22 to 150 carbon atoms, and usually not more than 1,5% of a parting agent, e.g. a higher aliphatic acid having from 12 to 24 carbon atoms or mineral lubricating oils, polyvinyl stearate, polyethylene or paraffin wax are usually added. The term "polyvinyl chloride resins" includes homopolymers of vinyl chloride, copolymers of vinyl chloride with vinyl acetate, vinylidene chloride, maleic or fumaric acid or styrene and also mixtures of polyvinyl chloride with a minor proportion of other synthetic resins, e.g. chlorinated polyethylene or a copolymer of acrylonitrile, butadiene and styrene. In the examples the stabilizer compositions used are (a) barium laurate, cadmium laurate, trimethylol propane and p-nonyl phenol, (b) cadmium and zinc stearate, 2,6-ditertiary-butyl-p-cresol and trimethylol ethane, (c) cadmium t-butyl benzoate, para-tertiary-butyl phenol and trimethylol ethane, (d) barium laurate, cadmium benzoate, bisphenol A and dipentaerythritol, the resins in each case being polyvinyl chloride homopolymer or a copolymer of 87% vinyl chloride and 13% vinyl acetate. Specification 752,053 is referred to.
ES0268116A 1961-05-10 1961-06-10 Polyvinyl chloride stabiliser combinations and polyvinyl chloride resins stabilised thereby Expired ES268116A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US10901661A 1961-05-10 1961-05-10

Publications (1)

Publication Number Publication Date
ES268116A1 true ES268116A1 (en) 1961-11-16

Family

ID=22325356

Family Applications (1)

Application Number Title Priority Date Filing Date
ES0268116A Expired ES268116A1 (en) 1961-05-10 1961-06-10 Polyvinyl chloride stabiliser combinations and polyvinyl chloride resins stabilised thereby

Country Status (6)

Country Link
BE (1) BE605765A (en)
CH (1) CH475292A (en)
DE (1) DE1190659B (en)
ES (1) ES268116A1 (en)
GB (1) GB934644A (en)
NL (2) NL128295C (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103450597B (en) * 2013-08-30 2015-09-09 美轲(淮安)化学有限公司 PVC processes auxiliary heat stabilizer

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB811532A (en) * 1956-11-28 1959-04-08 Ferro Chemical Corp Improvements in or relating to plastic compositions

Also Published As

Publication number Publication date
BE605765A (en)
GB934644A (en) 1963-08-21
NL128295C (en)
NL268049A (en)
CH475292A (en) 1969-07-15
DE1190659B (en) 1965-04-08

Similar Documents

Publication Publication Date Title
US5488065A (en) Antimicrobial compositions
GB981284A (en) Polyvinyl chloride resin stabiliser systems and resin compositions stabilised therewith
ES461603A1 (en) Plasticized polyvinyl chloride resin composition containing molybdenum flame retardant and antimony compound smoke suppressant agent
GB892146A (en) Improved compositions comprising stabilised polymers of vinyl chloride
GB1212224A (en) Method of lessening early discoloration of polyvinyl chrloride resins when heated, and compositions therefor
GB1203155A (en) Method of lessening early discoloration of polyvinyl chloride resins when heated and compositions therefor
US3448067A (en) Chlorine-containing polymers stabilized with mixtures of metal salts of mono-esters,a polyol and an epoxy compound
US4272427A (en) Plasticized PVC
ES268116A1 (en) Polyvinyl chloride stabiliser combinations and polyvinyl chloride resins stabilised thereby
GB936506A (en) Improvements in or relating to polymer compositions
US3285868A (en) Polyvinyl chloride stabilized with mixtures comprising polyols, phenols and salts ofmonocarboxylic acids
GB1099731A (en) Polyvinyl chloride resin stabilization with keto acetic acid compounds
GB1036845A (en) Process for the manufacture of self-extinguishing polymer compositions
GB988955A (en) Rigid polyvinyl chloride resin compositions having increased resistance to deterioration
US4539354A (en) Stabilized ethylene/chlorotrifluoroethylene copolymer composition
KR910016844A (en) Stabilized Chlorine-Containing Polymer Composition
US3544510A (en) Mercaptal stabilized halogen-containing resins
GB1412994A (en) High temperature thermoplastic compounds
US4252705A (en) Resistance of polyvinyl chloride resins to discoloration during drying with N,N&#39;-diphenyl urea
US3296163A (en) Poly alpha olefins stabilized with dithio-oxamides and phenols
US5002702A (en) Stabilizer compositions comprising a thiophosphate and an organo tin compound
US4567214A (en) Flame retardant polyolefin compositions
GB1001304A (en) Improvements in or relating to stabilized vinyl halide resin compositions
US3396133A (en) Plastic compositions
US3661844A (en) Organic acyl thioacetal and thioketal stabilizers for halogenated resins