GB642039A - Improvements relating to mixed phthalate esters and compositions incorporating them - Google Patents

Improvements relating to mixed phthalate esters and compositions incorporating them

Info

Publication number
GB642039A
GB642039A GB20/48A GB2048A GB642039A GB 642039 A GB642039 A GB 642039A GB 20/48 A GB20/48 A GB 20/48A GB 2048 A GB2048 A GB 2048A GB 642039 A GB642039 A GB 642039A
Authority
GB
United Kingdom
Prior art keywords
carbon atoms
phthalate
alkyl
ester
acid
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
GB20/48A
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.)
Nopco Chemical Co
Original Assignee
Nopco Chemical 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
Application filed by Nopco Chemical Co filed Critical Nopco Chemical Co
Publication of GB642039A publication Critical patent/GB642039A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/76Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring
    • C07C69/80Phthalic acid esters

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

A mixed phthalate ester prepared by esterification of a fatty acyl-glycol mono-ester having from 8-18 carbon atoms in the acyl group with a mono-alkyl acid phthalate having from 1-12 carbon atoms in the alkyl group, e.g. preferably a phthalate ester of the formula <FORM:0642039/IV (a)/1> where R is alkyl or alkenyl of 1-12 carbon atoms, R1 is alkyl or alkenyl of 7-17 carbon atoms and n is 1-10 (see Group IV (b)), is employed as a plasticizer for butyl methacrylate and other acrylates, polystyrene, vinyl resins including the acetate, chloride, acetal, butyral and chloride-acetate copolymer, butadiene-acrylonitrile, butadiene-styrene, modified alkyd resins, phenol- and urea-formaldehyde resins, cellulose esters such as the acetate, acetate-butyrate, and nitrate, ethyl or benzyl cellulose and other ethers. In the general formula, R may be, for example, methyl, isopropyl, 2-ethylhexyl or lauryl, whilst R1CO- may be caprylyl, oleyl, or linoleyl, for example. The preferred ester is that in which R is butyl, R1CO- is derived from the fatty acids obtained on hydrolysis of coconut oil, i.e. mainly lauric acid, and n is 3. The plasticizers are incorporated by any known method into the polymer or resin. In the examples: (5-12), the preferred ester (see preceding) is incorporated, by the use of a mutual solvent, into the following: polyvinyl acetate, chloride-acetate, butyral, and chloride; polystyrene; ethyl cellulose; and butyl methacrylate polymer; (13), polyvinyl acetate is plasticized with a phthalate of the above general formula in which R is 2-ethylhexyl, R1CO- is derived from coconut fatty acids, and n is 3.ALSO:A mixed phthalate ester is prepared by esterification of a fatty acyl-glycol mono-ester having from 8-18 carbon atoms in the acyl group with a mono-alkyl acid phthalate having from 1-12 carbon atoms in the alkyl group. In a preferred form of the invention, a mixed phthalate ester of the formula <FORM:0642039/IV (b)/1> where R is alkyl or alkenyl of 1-12 carbon atoms, R1 is alkyl or alkenyl of 7-17 carbon atoms and n is 1-10, is prepared by esterifying the product obtained from phthalic anhydride and an alkanol or alkenol ROH of 1-12 carbon atoms (i.e. an acid phthalate) with a monoesterified ethylene glycol or polyethylene glycol of formula HO(C2H4O)nCOR1, the latter being prepared from R1COOH and HO(C2H4O)nH. Specified acids of formula R1COOH include caprylic, oleic, stearic and linoleic, whilst examples of the alcohol ROH include methanol, isopropanol, 2-ethylhexanol, isobutanol and lauryl alcohol. The acid R1COOH may be that obtained on hydrolyzing a natural fat. In the examples: (1) monobutyl phthalate (obtained from n-butanol and phthalic anhydride) is refluxed in naphtha in the presence of sulphuric acid with triethylene glycol of which one hydroxy group has been esterified with coconut fatty acids; by-product water is removed azeotropically; (2) n-butanol in the process of example (1) is replaced by 2-ethylhexanol; (3) mono-2-ethylhexyl phthalate is esterified with mono-oleyl ethylene glycol; (4) monomethyl phthalate is esterified with nonaethylene glycol, one hydroxyl group of which is esterified with capric acid.ALSO:A mixed phthalate ester prepared (see Group IV (b)) by esterification of a fatty acyl-glycol mono-ester having from 8-18 carbon atoms in the acyl group with a mono-alkyl acid phthalate having from 1-12 carbon atoms in the alkyl group, e.g. preferably an ester: <FORM:0642039/V/1> where R is alkyl or alkenyl of 1-12 carbon atoms, R1 is alkyl or alkenyl of 7-17 carbon atoms, and n is 1-10, is used to plasticize rubbery butadiene polymers, e.g. of chlorobutadienes such as chloroprene, polysulphide rubbers, and chlorinated rubber. The preferred ester is that in which R is butyl, R1CO-is derived from the fatty acid (mainly lauric) obtained from coconut oil, and n is 3. The plasticizers are incorporated into the rubber by any known method.
GB20/48A 1947-01-11 1948-01-01 Improvements relating to mixed phthalate esters and compositions incorporating them Expired GB642039A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US642039XA 1947-01-11 1947-01-11

Publications (1)

Publication Number Publication Date
GB642039A true GB642039A (en) 1950-08-23

Family

ID=22054264

Family Applications (1)

Application Number Title Priority Date Filing Date
GB20/48A Expired GB642039A (en) 1947-01-11 1948-01-01 Improvements relating to mixed phthalate esters and compositions incorporating them

Country Status (1)

Country Link
GB (1) GB642039A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1868981A1 (en) * 2005-04-12 2007-12-26 LG Chem, Ltd. Triethyleneglycol ester based plasticizer composition for polyvinyl chloride resin and method of preparing the same
CN111073440A (en) * 2019-12-02 2020-04-28 骆瑜 Architectural decorative coating capable of removing formaldehyde and preparation method thereof

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1868981A1 (en) * 2005-04-12 2007-12-26 LG Chem, Ltd. Triethyleneglycol ester based plasticizer composition for polyvinyl chloride resin and method of preparing the same
CN101155772B (en) * 2005-04-12 2011-05-25 Lg化学株式会社 Triethyleneglycol ester based plasticizer composition for polyvinyl chloride resin and method of preparing the same
EP1868981A4 (en) * 2005-04-12 2011-08-10 Lg Chemical Ltd Triethyleneglycol ester based plasticizer composition for polyvinyl chloride resin and method of preparing the same
EP2455361A3 (en) * 2005-04-12 2014-04-02 Lg Chem, Ltd. Triethyleneglycol ester based plasticizer composition for polyvinyl chloride resin
CN111073440A (en) * 2019-12-02 2020-04-28 骆瑜 Architectural decorative coating capable of removing formaldehyde and preparation method thereof

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