GB741646A - Improvements in the production of rubber-resin products - Google Patents
Improvements in the production of rubber-resin productsInfo
- Publication number
- GB741646A GB741646A GB36314/53A GB3631453A GB741646A GB 741646 A GB741646 A GB 741646A GB 36314/53 A GB36314/53 A GB 36314/53A GB 3631453 A GB3631453 A GB 3631453A GB 741646 A GB741646 A GB 741646A
- Authority
- GB
- United Kingdom
- Prior art keywords
- resin
- rubber
- products
- components
- condensation product
- 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
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L21/00—Compositions of unspecified rubbers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L7/00—Compositions of natural rubber
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
- C08L9/06—Copolymers with styrene
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)
- Processes Of Treating Macromolecular Substances (AREA)
Abstract
Rubber/resin condensation products are produced by acidifying an acid-stabilized conjugated diolefin rubber latex and completely condensing therein the components or partial condensation product of a synthetic resin. The latex may be of natural rubber or of a synthetic rubber such as butadiene polymers and copolymers with styrene or acrylonitrile. The resin components may be aldehydes, such as formaldehyde and furfural, together with primary amines and substituted phenols, such as aniline, p-toluidine, resorcinol, m-amino-phenol and phloroglucinol, or with melamine, urea, thiourea, guanidine or dicyandiamide. Stabilizers specified are oleyl alcohol/ethylene oxide condensation product, cetyl pyridinium bromide and other cationic and non-ionic surface active agents described in U.S.A. Specifications 2,555,068 and 2,661,340. The acids used, e.g. hydrochloric or sulphuric, are preferably added in an amount sufficient to catalyse the reaction, during which bonding between the resin and rubber is said to occur. The resulting mixture is neutralized and the product may be recovered by the usual methods, e.g. coagulation. Ebonite or leather-like or rubbery products may be obtained and those containing up to 70 per cent resin may be plasticized, e.g. with petroleum residues, compounded and vulcanized with the usual ingredients. Fillers such as carbon black, magnesium oxide, zinc oxide, wood flour, chalk, cryptocrystalline clays and calcium silicate may be included and products suitable for shoesoles may be obtained.ALSO:Natural rubber/resin condensation products are produced by acidifying an acid-stabilized latex and condensing therein the components or partial condensation product of a synthetic resin. The resin components may be aldehydes, such as formaldehyde and furfural, together with primary amines and substituted phenols, such as aniline, p-toluidine, resorcinol, m-aminophenol and phloroglucinol, or with melamine, urea, thiourea, guanidine, or dicyandiamide. Stabilizers specified are oleyl alcohol/ethylene oxide condensation product, cetyl pyridinium bromide and other cationic and non-ionic surface active agents as listed in U.S.A. Specifications 2,555,068 and 2,661,340. The acids used, e.g. hydrochloric or sulphuric, are preferably added in an amount sufficient to catalyse the reaction, during which bonding between the resin and rubber is said to occur. The resulting mixture is neutralized and the product may be recovered by the usual methods. Ebonite or leather-like or rubbery products may be obtained and those containing up to 70 per cent resin may be plasticized, compounded and vulcanized with the usual ingredients. Fillers such as carbon black, magnesium and zinc oxides, wood flow, chalk, cryptocrystalline clays and calcium silicate may be included and products suitable for shoe-soles may be obtained.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL741646X | 1953-01-10 | ||
NL781411X | 1955-01-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB741646A true GB741646A (en) | 1955-12-07 |
Family
ID=26645066
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB36314/53A Expired GB741646A (en) | 1953-01-10 | 1953-12-31 | Improvements in the production of rubber-resin products |
GB35858/55A Expired GB781411A (en) | 1953-01-10 | 1955-12-14 | Improvements in the preparation of rubber-resin products from latex |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB35858/55A Expired GB781411A (en) | 1953-01-10 | 1955-12-14 | Improvements in the preparation of rubber-resin products from latex |
Country Status (4)
Country | Link |
---|---|
BE (2) | BE543713A (en) |
FR (2) | FR1090331A (en) |
GB (2) | GB741646A (en) |
NL (2) | NL84696C (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1720301A1 (en) * | 1966-10-05 | 1972-03-23 | Bp Chem Int Ltd | Process for the production of modified resins |
US3715172A (en) * | 1971-01-12 | 1973-02-06 | Nalco Chemical Co | Urea- and melamine- formaldehyde bridging agents |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1158245B (en) * | 1956-03-26 | 1963-11-28 | Continental Gummi Werke Ag | Process for welding vulcanized or partially vulcanized mixtures based on butadiene-acrylonitrile copolymers in a high-frequency alternating electric field |
NL134523C (en) * | 1963-08-23 |
-
0
- BE BE525302D patent/BE525302A/xx unknown
- BE BE543713D patent/BE543713A/xx unknown
- NL NL81034D patent/NL81034C/xx active
- NL NL84696D patent/NL84696C/xx active
-
1953
- 1953-12-30 FR FR1090331D patent/FR1090331A/en not_active Expired
- 1953-12-31 GB GB36314/53A patent/GB741646A/en not_active Expired
-
1955
- 1955-12-14 GB GB35858/55A patent/GB781411A/en not_active Expired
-
1956
- 1956-01-03 FR FR69188D patent/FR69188E/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1720301A1 (en) * | 1966-10-05 | 1972-03-23 | Bp Chem Int Ltd | Process for the production of modified resins |
US3715172A (en) * | 1971-01-12 | 1973-02-06 | Nalco Chemical Co | Urea- and melamine- formaldehyde bridging agents |
Also Published As
Publication number | Publication date |
---|---|
NL84696C (en) | |
BE525302A (en) | |
FR1090331A (en) | 1955-03-29 |
BE543713A (en) | |
NL81034C (en) | |
GB781411A (en) | 1957-08-21 |
FR69188E (en) | 1958-10-22 |
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