GB1092963A - Improvements relating to the curing of unsaturated polyester resins - Google Patents

Improvements relating to the curing of unsaturated polyester resins

Info

Publication number
GB1092963A
GB1092963A GB5145765A GB5145765A GB1092963A GB 1092963 A GB1092963 A GB 1092963A GB 5145765 A GB5145765 A GB 5145765A GB 5145765 A GB5145765 A GB 5145765A GB 1092963 A GB1092963 A GB 1092963A
Authority
GB
United Kingdom
Prior art keywords
peroxycyclopentane
water
present
unsaturated polyester
esters
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
GB5145765A
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.)
US Filter Wallace and Tiernan Inc
Original Assignee
Wallace and Tiernan 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.)
Filing date
Publication date
Application filed by Wallace and Tiernan Inc filed Critical Wallace and Tiernan Inc
Publication of GB1092963A publication Critical patent/GB1092963A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C08F283/00Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
    • C08F283/01Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to unsaturated polyesters

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Macromonomer-Based Addition Polymer (AREA)

Abstract

Unsaturated polyester resins are homopolymerized or copolymerized with an ethylenically unsaturated comonomer using as catalyst 3,5 - dimethyl - 3,5 - dihydroxy - 1,2 - peroxycyclopentane. The peroxycyclopentane is employed as a paste or liquid composition in an organic liquid selected from alkanols, glycols, ethers, ketones, esters, heterocyclic amides and heterocyclic alcohols. Mixtures of two or more of such liquids may be present and water is also preferably present. Conventional metal activators and inhibitors may be present. In the examples, an unsaturated polyester formed from maleic and phthalic anhydrides and propylene glycol is copolymerized with styrene, in the presence of hydroquinone, using (a) the peroxycyclopentane, water, N - methyl-2-pyrrolidinone and triethyl phosphate; (b) cobalt naphthenate plus (a); (c) the peroxycyclopentane, water and N-methyl-2-pyrrolidone; and (d) the peroxycyclopentane, water and "Cellosolve" (R.T.M.) acetate. In (c) and (d) glass fibre laminates are formed. Two component systems comprising (i) resin + promoter, and (ii) the peroxide catalyst system may be formed.ALSO:A stable solution of 3,5-dimethyl-3,5-dihydroxy - 1,2 - peroxycyclopentane is formed by using as solvent an organic liquid selected from alkanols, glycols including ether glycols, ethers, ketones, esters, heterocyclic amides and heterocyclic alcohols. Mixtures of two or more of such liquids may be used and water is preferably also present. Instead of a solution a paste may be formed by dispersing solid peroxycyclopentane in the organic liquid which is preferably a phthalate ester. The concentration of the peroxycyclopentane is preferably such that the formulation has an active oxygen content of from 1 to 6% by weight. Preferably at least part of the solvent is an N-alkyl-2-pyrrolidone in which the alkyl group contains 1 to 4 carbon atoms. Other preferred solutions are those in which at least part of the organic solvent is a propylene glycol or tetrahydrofurfuryl alcohol. Phosphate esters such as triethyl phosphate are preferably added to increase the burning resistance.
GB5145765A 1964-12-03 1965-12-03 Improvements relating to the curing of unsaturated polyester resins Expired GB1092963A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US41579964A 1964-12-03 1964-12-03

Publications (1)

Publication Number Publication Date
GB1092963A true GB1092963A (en) 1967-11-29

Family

ID=23647235

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5145765A Expired GB1092963A (en) 1964-12-03 1965-12-03 Improvements relating to the curing of unsaturated polyester resins

Country Status (4)

Country Link
DE (1) DE1569556C3 (en)
FR (1) FR1459477A (en)
GB (1) GB1092963A (en)
NL (1) NL146179B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2153168A1 (en) * 1970-11-02 1972-05-04 Koninkl Ind Mij Noury U V Pastes containing organic peroxides and processes for their preparation
WO1999057191A1 (en) * 1998-05-01 1999-11-11 Flowtite Technology As Peroxide blend compositions and methods for curing polyester resins

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2153168A1 (en) * 1970-11-02 1972-05-04 Koninkl Ind Mij Noury U V Pastes containing organic peroxides and processes for their preparation
FR2113460A5 (en) * 1970-11-02 1972-06-23 Koninkl Ind
WO1999057191A1 (en) * 1998-05-01 1999-11-11 Flowtite Technology As Peroxide blend compositions and methods for curing polyester resins

Also Published As

Publication number Publication date
DE1569556A1 (en) 1970-05-06
NL146179B (en) 1975-06-16
DE1569556B2 (en) 1973-03-08
FR1459477A (en) 1966-11-18
DE1569556C3 (en) 1979-11-22
NL6515460A (en) 1966-06-06

Similar Documents

Publication Publication Date Title
GB1176223A (en) Anaerobic Adhesive Composition
ES2057715T3 (en) UNSATURATED PHENONE DERIVATIVES AND THEIR USE AS ADHESIVE ADHESIVES.
GB961953A (en) Improvements in or relating to casting compounds
GB1244576A (en) PREPARATION OF beta-DIMETHYLAMINO ETHYL METHACRYLATE
GB865408A (en) Protective coatings for polyester resins
GB1092963A (en) Improvements relating to the curing of unsaturated polyester resins
JPS5461282A (en) Mixed esters of acidic succinate and aliphatic monoacylat of cellulose ether
GB1186777A (en) Cyanovinylated Heterocyclic Compounds and their use as Ultraviolet Light Absorbers
FI913398A0 (en) BINDEMEDEL FOER UV-HAERDANDE BELAEGGNINGSMEDEL, FOERFARANDE FOER DESS FRAMSTAELLING OCH DESS ANVAENDNING I BELAEGGNINGSMEDEL FOER POROESA OCH / ELLER SUGANDE UNDERLAG.
GB1301153A (en) Process for the production of abrasion-resistant cellulose-containing material
JPS5740507A (en) Peroxide mixture composition
ES369039A1 (en) Method of manufacture of resinous products from epoxy compounds
JPS5527324A (en) Composition for powder coating
GB1169859A (en) New 2-Phenyl-Benzotriazoles
GB1173711A (en) Diepoxyalkyl Esters of Bicyclo[2,2,1]Heptane-2,3-Dicarboxylic Acids
ES2154630T3 (en) PROCEDURE FOR THE PREPARATION OF INTERPOLIMERO DISPERSIONS FROM VINYL ESTERS OF CARBOXYLIC ACIDS OF RAMIFIED CHAIN AND ETHENICALLY INSATURED ACIDS AND / OR ITS ESTERS.
GB984827A (en)
US3349040A (en) Peroxide curing of unsaturated polyester resins and formulations therefor
FR2300063A1 (en) 3-Hydroxymethyl-diphenyl ether prepn - by condensing phenol with m-cresol, oxidising ether to 3-carboxy-diphenyl ether, esterifying, and reducing
GB915009A (en) Process for the manufacture of explosion-proof peroxide solutions
JPS5566912A (en) Carboxylation of ethylene polymer
JPS5582112A (en) Resin composition for fiber-reinforcing
JPS56159239A (en) Modified polyolefin composition
GB1287760A (en) PROCESS FOR THE MANUFACTURE OF 17alpha-ACYLOXY-20-KETO-STEROIDS
JPS5512156A (en) Copolymerization of epoxy compound with carbon dioxide