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GB589650A - - Google Patents

Info

Publication number
GB589650A
GB589650A GB1562444A GB1562444A GB589650A GB 589650 A GB589650 A GB 589650A GB 1562444 A GB1562444 A GB 1562444A GB 1562444 A GB1562444 A GB 1562444A GB 589650 A GB589650 A GB 589650A
Authority
GB
United Kingdom
Prior art keywords
allyl
acids
methallyl
beta
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
GB1562444A
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 filed Critical
Publication of GB589650A publication Critical patent/GB589650A/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
    • C08F8/00Chemical modification by after-treatment
    • C08F8/12Hydrolysis
    • 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
    • C08F218/00Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid or of a haloformic acid
    • C08F218/02Esters of monocarboxylic acids
    • C08F218/04Vinyl esters
    • 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
    • C08F240/00Copolymers of hydrocarbons and mineral oils, e.g. petroleum resins
    • 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
    • C08F2810/00Chemical modification of a polymer
    • C08F2810/20Chemical modification of a polymer leading to a crosslinking, either explicitly or inherently

Landscapes

  • Chemical & Material Sciences (AREA)
  • General 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)
  • Polysaccharides And Polysaccharide Derivatives (AREA)

Abstract

589,650. Polyallyl esters. SHELL DEVELOPMENT CO. Aug. 16, 1944, No. 15624. Convention date, Aug. 11, 1943. [Class 2 (iii)] [Also in Group VIII] Polyallyl type esters or polyallyl type alcohols obtained by hydrolysis or alcoholysis' of polyallyl type esters are heated with unsaturated acids, or a mixture of such acids, or anhydrides or acid halides of unsaturated acids. Polyallyl type esters specified are polymeric allyl formate, acetate, propionate, butyrate, isobutyrate, beta-methallyl acetate, beta chlorallyl acetate, beta ethallyl formate, beta phenyl allyl acetate, beta methoxy allyl acetate, beta chloromethylallyl acetate, allyl benzoate, toluate, salicylate, glycollate, methoxyacetate, beta methallyl chloracetate, allyl beta chlorpropionate, lactate, naphthenate, alpha hydroxy isobutyrate, acetyl glycollate, stearate, levulinate, ethoxy formate, naphthoate, abietate, diallyl malonate, succinate, adipate, maleate, phthalate, beta methallyl chlorobenzoate, chloroacetate, butyrate and alpha methallyl acetate, alpha phenylallyl acetate, beta methallyl phenoxyformate, diallyl diglycollate, dilactate, dihydracrylate, dimethallyl diglycollate, dicrotyl dilactate, allyl halides and allyl type esters of ortho acids of boron and silicon.. The polymers of the allyl-type esters or allyl type alcohols obtained therefrom may be air blown, hydrogenated or treated with sulphur dioxide before heating with the unsaturated acid. 'Unsaturated acids specified are palmitoleic, oleic, linoleic, linolenic, arachidonic, clupanodonic, elaeostauric, licanic acids, 9-11 linoleic, octadecadienic and ricinic acids and commercial mixtures obtained from chia, hempseed, linseed, perilla, sunflower, soyabean, walnut, poppyseed, sunflower oils, oiticica, Japanese wood, walnut seed, rubber seed, dehydrated castor and tall oils. Saturated acids and alcohols may be present. Driers may be added such as red lead, litharge, manganese dioxide, cobalt, lead and manganese resinates, linoleates and naphthenates, manganese, calcium and zinc borates, lead acetate and carbonate, blowing with oxygen, ozone, hydrogen peroxide, sodium, calcium, barium and benzoyl peroxides, perborates and percarbonates: Dyes, fillers, solvents and artificial and natural resins may be added such as resin, colophony, shellac, copal, dammar gun, pitch, asphalt, protein plastics, cellulose derivatives, phenol aldehyde, urea aldehyde, alkyd, super polyamides and ester resins, polymers of vinyl, allyl and methallyl esters of acetic, propionic and butyric acids, of methyl, ethyl and propyl esters of acrylic and methacrylic acids, styrene, alpha methyl styrene, ethylene,of vinyl and vinylidene halides, of allyl alcohol and halides, polyvinyl acetals and after chlorinated polyvinyl chloride, polymers of vinyl, allyl and methallyl esters of oxalic, malonic, succinic, glutaric, citric, tartaric, phthalic, isophthalic, naphthalene dicarboxylic, acrylic and methacrylic acids, vinyl, allyl, methallyl and cyclohexinyl esters of ortho acids of boron and silicon, sulphuric and phosphoric acids, polymers of acrylic and methacrylic esters of glycol, diethylene glycol, triethylene glycol, trimethylene glycol and glycerol, poly ethers of vinyl, allyl and methallyl with glycol, triethylene glycol, trimethylene glycol, diethylene glycol and glycerol, polymers of vinyl, allyl, methallyl and crotyl diethers, polymers of butadiene, pentadiene, mono vinyl acetylene and divinyl acetylene. Esterification of the polyallyl type alcohols may be carried out in the presence of water admixed with kerosene, high boiling ethers or solvent naphthas. Specification 566,344 is referred to.
GB1562444A 1947-12-29 1944-08-16 Expired GB589650A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
NL137710A NL68954C (en) 1947-12-29 1947-12-29

Publications (1)

Publication Number Publication Date
GB589650A true GB589650A (en) 1947-06-26

Family

ID=63788245

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1562444A Expired GB589650A (en) 1947-12-29 1944-08-16

Country Status (2)

Country Link
GB (1) GB589650A (en)
NL (1) NL68954C (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3226347A (en) * 1960-01-16 1965-12-28 Resines Et Vernis Artificiels Process for the preparing of thixotropic gelled resins, products resulting therefrom, and applications thereof
MD4209C1 (en) * 2012-03-30 2013-10-31 Институт Химии Академии Наук Молдовы Process for producing sclareoloxide

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3226347A (en) * 1960-01-16 1965-12-28 Resines Et Vernis Artificiels Process for the preparing of thixotropic gelled resins, products resulting therefrom, and applications thereof
MD4209C1 (en) * 2012-03-30 2013-10-31 Институт Химии Академии Наук Молдовы Process for producing sclareoloxide

Also Published As

Publication number Publication date
NL68954C (en) 1951-11-15

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