GB758724A - Improvements relating to synthetic resins - Google Patents

Improvements relating to synthetic resins

Info

Publication number
GB758724A
GB758724A GB24009/53A GB2400953A GB758724A GB 758724 A GB758724 A GB 758724A GB 24009/53 A GB24009/53 A GB 24009/53A GB 2400953 A GB2400953 A GB 2400953A GB 758724 A GB758724 A GB 758724A
Authority
GB
United Kingdom
Prior art keywords
acids
alcohol
peroxide
copolymer
reacting
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
GB24009/53A
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.)
Lewis Berger and Sons Ltd
Original Assignee
Lewis Berger and Sons Ltd
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 Lewis Berger and Sons Ltd filed Critical Lewis Berger and Sons Ltd
Publication of GB758724A publication Critical patent/GB758724A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule

Landscapes

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

Abstract

A synthetic resin for use in paints, varnishes and baking enamels is the reaction product of a copolymer of an unsaturated monocarboxylic fatty acid and a monovinyl aromatic compound, a polyhydric alcohol and a polysiloxane containing alkoxy groups, and/or halogen atoms. The resin may be made by reacting the siloxane with the alcohol and with the copolymer, but is preferably made by reacting the alcohol with the copolymer and reacting the resulting ester with the siloxane. There are specified (a) monovinyl aromatic compounds-styrene, a - methylstyrene, p-methylstyrene, a -p-dimethylstyrene, divinylbenzene, vinylnaphthalene, acenaphthylene, vinyltoluene, p-chlorostyrene, p-trichloromethylstyrene, 2 : 5-dichlorostyrene, p-methoxystyrene or mixtures thereof; (b) unsaturated fatty acids-acrylic, methacrylic, vinylacetic, hydrosorbic, decenoic, undecylenic, sorbic, hiragonic, linoleic, isolinoleic, elaeostearic, punicic, parinaric, arachidonic, clupanodonic, scoliodonic, nisinic, tariric, abietic and licanic acids; castor-, linseed-, soyabean-and tung-oil fatty acids, rosin acids and tall oil acids; the dimers and trimers of these acids may also be used; (c) polyhydric alcohols-ethylene-, diethylene-, propylene- and trimethylene-glycols, glycerine, trimethylol propane, pentaerythritol, polyallyl alcohol, sorbito-and mannitol. The alkoxy polysiloxanes specified conform to the formula <FORM:0758724/IV(a)/1> where R is a lower alkyl radical (i.e. of 1 to 4 C atoms), R1 is an alkyl or aryl radical, R11 is R1 or alkoxy and n is at least 2. The halogenopolysiloxanes specified are dimethyltriphenyltrichlorotrisiloxane and trimethyltriphenyldichlorotrisiloxane. In making the copolymers, the proportions by weight are preferably 5 to 75 per cent of the vinyl monomer and 95 to 25 per cent of the acid, and the reaction is desirably effected under reflux at 150 DEG to 475 DEG F. in the presence of a solvent and a catalyst or controlling agent, e.g. hydrogen peroxide, benzoyl peroxide, t-butyl peroxide, di-tertiary butyl peroxide, acetyl peroxide in dimethyl phthalate, fuller's earth, sulphur, sulphur dioxide, stannic chloride, boron trifluoride or a redox catalyst such as a mixture of dodecyl mercaptan and benzoyl peroxide or benzidine and sulphur dioxide, and desirably in an inert atmosphere, e.g. nitrogen or carbon dioxide. Examples A1 to A19 describe the preparation of the copolymers and examples B1 to B13 describe the preparation of the resinous reaction products. U.S.A. Specifications 2,415,389, 2,584,343 and 2,587,295 are referred to.
GB24009/53A 1952-09-09 1953-08-31 Improvements relating to synthetic resins Expired GB758724A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US758724XA 1952-09-09 1952-09-09

Publications (1)

Publication Number Publication Date
GB758724A true GB758724A (en) 1956-10-10

Family

ID=22128501

Family Applications (1)

Application Number Title Priority Date Filing Date
GB24009/53A Expired GB758724A (en) 1952-09-09 1953-08-31 Improvements relating to synthetic resins

Country Status (1)

Country Link
GB (1) GB758724A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8258188B2 (en) 2004-01-20 2012-09-04 Josep Bassaganya-Riera Method of using punicic acid to enhance immune response and prevent metabolic disorders

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8258188B2 (en) 2004-01-20 2012-09-04 Josep Bassaganya-Riera Method of using punicic acid to enhance immune response and prevent metabolic disorders
US8822543B2 (en) 2004-01-20 2014-09-02 Nutrition Therapeutics, Inc. Method of using punicic acid to enhance immune response and prevent metabolic disorders

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