GB625576A - Improvements in or relating to synthetic resinous compositions and to products formed therefrom - Google Patents
Improvements in or relating to synthetic resinous compositions and to products formed therefromInfo
- Publication number
- GB625576A GB625576A GB19867/46A GB1986746A GB625576A GB 625576 A GB625576 A GB 625576A GB 19867/46 A GB19867/46 A GB 19867/46A GB 1986746 A GB1986746 A GB 1986746A GB 625576 A GB625576 A GB 625576A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- polyvinyl
- phenol
- added
- formaldehyde
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G8/00—Condensation polymers of aldehydes or ketones with phenols only
- C08G8/04—Condensation polymers of aldehydes or ketones with phenols only of aldehydes
- C08G8/08—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ
- C08G8/12—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ with monohydric phenols having only one hydrocarbon substituent ortho on para to the OH group, e.g. p-tert.-butyl phenol
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G8/00—Condensation polymers of aldehydes or ketones with phenols only
- C08G8/04—Condensation polymers of aldehydes or ketones with phenols only of aldehydes
- C08G8/08—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ
- C08G8/10—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ with phenol
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/04—Condensation polymers of aldehydes or ketones with phenols only
- C08L61/06—Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L29/00—Compositions of homopolymers or copolymers 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 alcohol, ether, aldehydo, ketonic, acetal or ketal radical; Compositions of hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Compositions of derivatives of such polymers
- C08L29/02—Homopolymers or copolymers of unsaturated alcohols
- C08L29/04—Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L29/00—Compositions of homopolymers or copolymers 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 alcohol, ether, aldehydo, ketonic, acetal or ketal radical; Compositions of hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Compositions of derivatives of such polymers
- C08L29/14—Homopolymers or copolymers of acetals or ketals obtained by polymerisation of unsaturated acetals or ketals or by after-treatment of polymers of unsaturated alcohols
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L31/00—Compositions of homopolymers or copolymers 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; Compositions of derivatives of such polymers
- C08L31/02—Homopolymers or copolymers of esters of monocarboxylic acids
- C08L31/04—Homopolymers or copolymers of vinyl acetate
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
A synthetic resinous composition hardenable at room or moderately raised temperature comprises a mixture of phenol-formaldehyde resol, an acid accelerator and 0.1-15 per cent of polyvinyl acetate, of partly hydrolysed polyvinyl acetate, of polyvinyl alcohol, or mixtures of two or more of these materials. The resol is formed from a phenol or a cresol and may be solid, liquid or a solution or dispersion of solid resin. Suitable accelerators are hydrochloric, sulphuric or a sulphonic acid. The accelerator is preferably added just before hardening, but the polyvinyl compound may be added to the phenol before reaction with the formaldehyde or during or after the reaction with the formaldehyde. The polyvinyl compound may be mixed with the acid accelerator. They may be dissolved or dispersed in solvents before incorporation. The products may be cast, used as adhesives, for the formation of expanded resins by inclusion of a gas generator or they may be dissolved to form lacquers or varnishes. Suitable solvents are methyl ethyl or butyl alcohol, methyl ethyl ketone or ethyl acetate. In examples: (1) phenol and /or aldehyde were refluxed with sodium hydroxide and the product dehydrated. The liquid resin is mixed with an alcoholic solution of polyvinyl butyral and sulphuric acid added to harden the mixture. The product may be used for sticking synthetic resin mouldings or for securing bristles in their holders; (2) polyvinyl alcohol is used instead of the butyral and hydrochloric instead of sulphuric acid; (3) polyvinyl acetate is mixed with p-toluene sulphonic acid and the mixture added to a liquid resin as in example (1). The product in solution in methylated spirit may be applied to acid-resisting paper, and abrasive grit is sprinkled on and the composition air-dried. A sizing coat of the resinous composition may then be applied. Reference has been directed by the Comptroller to Specification 553,437.
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL65445D NL65445C (en) | 1946-07-03 | ||
BE474159D BE474159A (en) | 1946-07-03 | ||
GB19867/46A GB625576A (en) | 1946-07-03 | 1946-07-03 | Improvements in or relating to synthetic resinous compositions and to products formed therefrom |
FR948695D FR948695A (en) | 1946-07-03 | 1947-07-01 | Resin compositions based on phenolformaldehyde hardening under the effect of acids |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB19867/46A GB625576A (en) | 1946-07-03 | 1946-07-03 | Improvements in or relating to synthetic resinous compositions and to products formed therefrom |
GB948695X | 1946-07-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB625576A true GB625576A (en) | 1949-06-30 |
Family
ID=31980047
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB19867/46A Expired GB625576A (en) | 1946-07-03 | 1946-07-03 | Improvements in or relating to synthetic resinous compositions and to products formed therefrom |
Country Status (2)
Country | Link |
---|---|
FR (1) | FR948695A (en) |
GB (1) | GB625576A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2748046A (en) * | 1954-04-12 | 1956-05-29 | Crown Zellerbach Corp | Method of edge-surfacing woody products |
US2917483A (en) * | 1956-10-12 | 1959-12-15 | Shawinigan Resins Corp | Electrical insulation comprising polyvinyl acetal-phenol aldehydes cured with sulfuric acid |
WO2000075230A1 (en) * | 1998-03-02 | 2000-12-14 | Durez Corporation | Phenolic thermosetting resins containing polyols |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE956987C (en) * | 1951-06-20 | 1957-01-24 | Hoechst Ag | Process for the production of self-hardening masses that give permanent bonds against attack by chemical substances, especially against acids |
-
1946
- 1946-07-03 GB GB19867/46A patent/GB625576A/en not_active Expired
-
1947
- 1947-07-01 FR FR948695D patent/FR948695A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2748046A (en) * | 1954-04-12 | 1956-05-29 | Crown Zellerbach Corp | Method of edge-surfacing woody products |
US2917483A (en) * | 1956-10-12 | 1959-12-15 | Shawinigan Resins Corp | Electrical insulation comprising polyvinyl acetal-phenol aldehydes cured with sulfuric acid |
WO2000075230A1 (en) * | 1998-03-02 | 2000-12-14 | Durez Corporation | Phenolic thermosetting resins containing polyols |
Also Published As
Publication number | Publication date |
---|---|
FR948695A (en) | 1949-08-08 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2411557A (en) | Synthetic phenolic resins | |
US2414414A (en) | Method of bonding materials with a cold-setting dihydroxy benzene aldehyde adhesive | |
US3410718A (en) | Phenol-formaldehyde novolak-phenolformaldehyde resole molding surface for a reinforced matrix base sheet | |
GB625576A (en) | Improvements in or relating to synthetic resinous compositions and to products formed therefrom | |
US2422637A (en) | Resinous condensation product of phenol and styrene oxide | |
US3267053A (en) | Phenol-formaldehyde resin compositions | |
US4250076A (en) | Foundry molding compositions | |
US2675336A (en) | Phenolic resin | |
US2410395A (en) | Acid-curing synthetic resin combined with olefine-sulfur dioxide polymer | |
GB642306A (en) | Improvements in or relating to pressure-sensitive adhesive tape, and method of producing same | |
US3538052A (en) | Post-alkylated novolac resins wherein the alkylating material is a mixture of arylalkenes,arylcycloalkenes,dicyclopentadienes and cyclopentadiene/acyclic conjugated diene codimers | |
US2767154A (en) | Method of producing pigmented lacquers and the like | |
US3096226A (en) | Aqueous composition of phenol-aldehyde condensate and method of bonding materials with same | |
US2125594A (en) | Floor and wall covering material | |
GB928117A (en) | Curing phenolic resins | |
US2576735A (en) | Nitrogenous resins from ketonealdehyde-nitrogenous base and phenol-aldehyde | |
US2535020A (en) | Plasticized amino-aldehyde resins | |
FI73717B (en) | HALVTORR FORMALDEHYDFRI METOD ATT FRAMSTAELLA SPAONPLATTOR. | |
US2163264A (en) | Condensation products from formaldehyde and urea | |
US2956965A (en) | Plasticized phenolic-formaldehyde resin compositions | |
US2291843A (en) | Coating composition containing ester gum | |
GB562310A (en) | Improvements in or relating to the manufacture of drying oil compositions | |
US2321208A (en) | Organic solution of formaldehydeurea reaction product | |
GB843794A (en) | A process for the preparation of moulding sand for the shell moulding process | |
GB507013A (en) | Improvements in or relating to the production of synthetic resins |