GB629093A - Curing polymerizable materials - Google Patents

Curing polymerizable materials

Info

Publication number
GB629093A
GB629093A GB1593546A GB1593546A GB629093A GB 629093 A GB629093 A GB 629093A GB 1593546 A GB1593546 A GB 1593546A GB 1593546 A GB1593546 A GB 1593546A GB 629093 A GB629093 A GB 629093A
Authority
GB
United Kingdom
Prior art keywords
methyl
stands
allyl
polymerized
crotyl
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
GB1593546A
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.)
ARTHUR MARK HOWALD
Libbey Owens Ford Glass Co
Original Assignee
ARTHUR MARK HOWALD
Libbey Owens Ford Glass 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 ARTHUR MARK HOWALD, Libbey Owens Ford Glass Co filed Critical ARTHUR MARK HOWALD
Priority to GB1593546A priority Critical patent/GB629093A/en
Publication of GB629093A publication Critical patent/GB629093A/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
    • C08F4/00Polymerisation catalysts
    • C08F4/28Oxygen or compounds releasing free oxygen
    • C08F4/32Organic compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Paints Or Removers (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

<FORM:0629093/IV (a)/1> Substances having a plurality of unconjugated double bonds are polymerized in thick sections by heating at below 180 DEG F. in the presence of an organic peroxide or ozonide, and a cobalt, iron, copper or manganese drier, the inhibitory effect of oxygen present at the surface being counteracted by the metallic drier. The thick section may comprise plies of inert materials. The polymerizable substances specified are diallyl, -crotyl, -methallyl, -alpha methyl allyl, -beta chloroallyl, -beta methyl crotyl esters of maleic, chloromaleic, bromomaleic, fumaric, chlorofumaric, bromofumaric, mesaconic, citraconic, itaconic, carbonic, oxalic, malonic, succinic, glutaric, adipic, pimelic, suberic, az<\>gelaic, sebacic, benzene-, diphenyl-, cyclohexane- or naphthalenedicarboxylic acids, or pyrotartaric acid. Other compounds which can be so polymerized are of the formul in Figs. 2, 3, 4, 5 and 6, in which F stands for an acrylic, methacrylic or a -chloracrylic acid group, B stands for a methylene, methyl methylene or phenylene group. Ru stands for an allyl, crotyl, a -methyl allyl, b -methyl allyl, b -chloro-allyl or b -methyl crotyl group, Du stands for a maleic, chloromaleic, bromomaleic, fumaric, chloro- and bromofumaric, mesaconic, citraconic or itaconic acid group, Rs stands for a methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec. butyl or tert. butyl alcohol group, D stands for all the di-basic acids listed above, E stands for ethylene glycol, propylene glycol, 1,2-butylene glycol, 2,3-butylene glycol, trimethylene glycol, tetramethylene-, pentamethylene-, hexamethylene-, heptamethylene-, octamethylene-glycols, and diethylene-, triethylene- and tetraethylene-glycols, and o-, m- or p-dihydroxybenzene. Driers specified are cobalt, iron, copper and manganese naphthenates, resinates, linoleates or salts of other unsaturated acids. Peroxides and ozonides specified are benzoyl, succinyl, acetyl, toluyl, p-bromobenzoyl, anisoyl, chloroacetyl and furoyl peroxides, peracetic and perbenzoic acids, di-isopropylene ozonide, and diisobutylene ozonide. Inhibitors such as hydroquinone, pyrogallol, tannic acid, aniline or phenylene diamine may be employed. When polyesters are to be polymerized excess polyhydric alcohol may be used and the excess hydroxy groups in the ester may be reacted with phosgene, acetyl chloride, chloroacetyl chloride, succinyl or benzoyl chlorides or silicon tetrachloride, or tetramethylene-, or octamethylene-di-isocyanate or phenyl isocyanate. An excess of polybasic acid may also be used when excess acidic groups may be reacted with a metallic base or with a monohydric alcohol or with an amine such as butylamine, aniline or phenylene diamine. If both free hydroxy and carboxy groups are present in the polyester successive reagents, as set out above, may be used. Styrene, vinyl acetate, methyl methacrylate or methyl acrylate may be used in conjunction with an unsaturated polyester. The substance to be polymerized may be used as a binder for laminated canvas or the like, or may be whipped into a foam to give, on polymerizing, a porous product. Specification 540,168 is referred to.
GB1593546A 1946-05-25 1946-05-25 Curing polymerizable materials Expired GB629093A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1593546A GB629093A (en) 1946-05-25 1946-05-25 Curing polymerizable materials

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1593546A GB629093A (en) 1946-05-25 1946-05-25 Curing polymerizable materials

Publications (1)

Publication Number Publication Date
GB629093A true GB629093A (en) 1949-09-12

Family

ID=10068189

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1593546A Expired GB629093A (en) 1946-05-25 1946-05-25 Curing polymerizable materials

Country Status (1)

Country Link
GB (1) GB629093A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3437715A (en) * 1955-04-15 1969-04-08 Pittsburgh Plate Glass Co Resin composition
EP0242791A2 (en) * 1986-04-25 1987-10-28 Ethyl Corporation Process for producing polymers of monoallylamine
WO2008107146A1 (en) * 2007-03-06 2008-09-12 Dsm Ip Assets B.V. Pre-accelerated resin composition

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3437715A (en) * 1955-04-15 1969-04-08 Pittsburgh Plate Glass Co Resin composition
EP0242791A2 (en) * 1986-04-25 1987-10-28 Ethyl Corporation Process for producing polymers of monoallylamine
EP0242791A3 (en) * 1986-04-25 1988-01-07 Ethyl Corporation Process for producing polymers of monoallylamine
WO2008107146A1 (en) * 2007-03-06 2008-09-12 Dsm Ip Assets B.V. Pre-accelerated resin composition
US20100087601A1 (en) * 2007-03-06 2010-04-08 Dsm Ip Assets B.V. Pre-accelerated resin composition
CN101627080B (en) * 2007-03-06 2012-09-26 帝斯曼知识产权资产管理有限公司 Pre-accelerated resin composition
US8501851B2 (en) 2007-03-06 2013-08-06 Dsm Ip Assets B.V. Pre-accelerated resin composition

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