GB1016952A - Plasticised halogen-containing resins - Google Patents

Plasticised halogen-containing resins

Info

Publication number
GB1016952A
GB1016952A GB2823862A GB2823862A GB1016952A GB 1016952 A GB1016952 A GB 1016952A GB 2823862 A GB2823862 A GB 2823862A GB 2823862 A GB2823862 A GB 2823862A GB 1016952 A GB1016952 A GB 1016952A
Authority
GB
United Kingdom
Prior art keywords
diallyl
reacting
radical
compound
ester
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
GB2823862A
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.)
Monsanto Co
Original Assignee
Monsanto Co
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
Priority claimed from US178542A external-priority patent/US3280067A/en
Application filed by Monsanto Co filed Critical Monsanto Co
Publication of GB1016952A publication Critical patent/GB1016952A/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
    • C08K5/10Esters; Ether-esters
    • C08K5/11Esters; Ether-esters of acyclic polycarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F259/00Macromolecular compounds obtained by polymerising monomers on to polymers of halogen containing monomers as defined in group C08F14/00
    • C08F259/02Macromolecular compounds obtained by polymerising monomers on to polymers of halogen containing monomers as defined in group C08F14/00 on to polymers containing chlorine
    • C08F259/04Macromolecular compounds obtained by polymerising monomers on to polymers of halogen containing monomers as defined in group C08F14/00 on to polymers containing chlorine on to polymers of vinyl chloride

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

A plastic composition comprises in uniform admixture a polymer of which at least 50% by weight is formed from a halogen-containing monomer having a terminal ethylenically unsaturated group and, as plasticizer therefor, a polymerizable fumaric acid ester composition, the said plastic composition further containing a polyallyl ester of a polybasic acid. The fumaric acid ester compositions may have the general formula <FORM:1016952/C3/1> where A is the fumaryl radical <FORM:1016952/C3/2> R is a divalent aliphatic or alicylic hydrocarbon or oxyhydrocarbon radical; R1 and R2 are each alkyl, cycloalkyl, alkenyl or aralkyl n is 0, 1 or 2; m and y are unlike and each is 0 or 1 and the sum of m+n is at least 1. They may be prepared as in Specification 997,172. The polyalkyl esters are esters of any allyl alcohol, substituted or unsubstituted, with a polybasic acid which is saturated or unsaturated. A substantially non-volatile alkyl substituted monoaryl compound may be added to improve the viscosity (hereinafter called an aryl alkane). Preferred aryl alkanes are obtained by (1) condensing an aromatic hydrocarbon of the benzene series with an acylic propylene polymer containing 12 to 18 carbon atoms and (2) mono-alkylating benzene with the product obtained by substantial mono-chlorination of paraffin base kerosene fractions. Peroxy compounds, fillers, stabilizers and colouring materials may be added. In the examples the halogen containing polymer is polyvinyl chloride and the polyallyl esters employed are diallyl adipate, diallyl phthalate, diallyl succinate, diallyl sebacate, diallyl oxalate, diallyl malonate, diallyl dimerate, diallyl diglycollate and triallyl citrate.ALSO:Fumaric acid esters of the general formula <FORM:1016952/C2/1> where A is the fumaryl radical <FORM:1016952/C2/2> R is a divalent aliphatic or alicyclic hydrocarbon or oxyhydrocarbon radical; R1 and R2 are each alkyl, cycloalkyl, alkenyl or aralkyl; n is 0, 1 or 2; m and y are unlike and are each 0 or 1 and the sum of m and n is at least 1 may be prepared by one of the following methods:- (1) Reacting a partial ester of maleic acid <FORM:1016952/C2/3> where X is an aliphatic or alicyclic hydrocarbon radical of valency X and X is a whole number from 2 to 6, with at least one hydroxy compound R1OH where R1 is alkyl, cycloalkyl, alkenyl or aralkyl, in the presence of a halogen-containing compound; (2) Reacting a fumaryl chloride of formula <FORM:1016952/C2/4> where R1 is above, with a polyhydroxy compound having 2 to 6 hydroxyl groups, the molar ratio of chloride to polyhydroxy compound being X:1 where X equals the number of hydroxyl groups; and (3) Reacting a fumarate ester of formula <FORM:1016952/C2/5> where R1 is as above, with a polyhydroxy compound having 2 to 6 hydroxyl groups, the molar ratio of the fumarate ester to polyhydroxy compound being 1 to 1.5 X: 1 where X is the number of hydroxyl groups. In the examples fumaric acid esters are formed by (1) reacting isobutyl fumaryl chloride with 1,3-butanediol and (2) reacting the following dialkyl fumarates with the following polyhydroxy compounds :- diisohexyl, dibutyl, dimethylamyl, diiso-octyl, diisohexyl, di-2-ethylhexyl or diisobutyl fumarates and 1,2-, 1,3- or 1,4-butanediol; neopentyl glycol; dipropylene glycol and di- or triethylene glycol.
GB2823862A 1961-04-03 1962-07-23 Plasticised halogen-containing resins Expired GB1016952A (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US10002661A 1961-04-03 1961-04-03
US12595161A 1961-07-24 1961-07-24
US178542A US3280067A (en) 1961-04-03 1962-03-09 Plasticized halogen-containing resins
US19536862A 1962-05-21 1962-05-21

Publications (1)

Publication Number Publication Date
GB1016952A true GB1016952A (en) 1966-01-12

Family

ID=26824123

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2823862A Expired GB1016952A (en) 1961-04-03 1962-07-23 Plasticised halogen-containing resins

Country Status (1)

Country Link
GB (1) GB1016952A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2455486A1 (en) * 1979-05-04 1980-11-28 Matec Holding COATING METHOD FOR FLAT ELEMENTS AND COATING LAYER

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2455486A1 (en) * 1979-05-04 1980-11-28 Matec Holding COATING METHOD FOR FLAT ELEMENTS AND COATING LAYER

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