GB946379A - Process for producing phenol-modified coumarone-indene type resins - Google Patents
Process for producing phenol-modified coumarone-indene type resinsInfo
- Publication number
- GB946379A GB946379A GB625762A GB625762A GB946379A GB 946379 A GB946379 A GB 946379A GB 625762 A GB625762 A GB 625762A GB 625762 A GB625762 A GB 625762A GB 946379 A GB946379 A GB 946379A
- Authority
- GB
- United Kingdom
- Prior art keywords
- reaction mixture
- temperature
- acids
- catalyst
- naphtha
- 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
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F240/00—Copolymers of hydrocarbons and mineral oils, e.g. petroleum resins
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (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 process for producing phenol-modified coumarone-indene resins comprising polymerizing an anhydrous mixture of an essentially aromatic naphtha boiling principally in the range 160 to 200 DEG C. in which indene is the principal polymerizable constituent, and anhydrous cresylic acids, in proportions such that a small excess of said acids remain in the reaction mixture when the reaction is terminated, in the presence of an organic complex of boron trifluoride at a temperature not in excess of 110 DEG C. until the specific gravity of the reaction mixture becomes substantially constant, neutralising the catalyst, removing unreacted materials from the reaction mixture and recovering the alcohol-soluble phenol-modified product. In one modification the naphtha and cresylic acids are mixed and the catalyst thereafter added incrementally at such a rate that the temperature does not exceed 110 DEG C. In another modification the cresylic acids and catalyst are mixed, preferably together with an aromatic hydrocarbon boiling above the reaction temperature but below 300 DEG C., and the naphtha added at such a rate that the temperature of the reaction mixture does not exceed 110 DEG C. The first modification may give predominantly solid products and the second predominantly liquid products. The preferred organic complexes are those of boron trifluoroide with alkyl ethers and alkanoic acids, e.g. methyl ethyl ether, diethyl ether, dipropyl ether, acetic acid and propionic acid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB625762A GB946379A (en) | 1962-02-19 | 1962-02-19 | Process for producing phenol-modified coumarone-indene type resins |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB625762A GB946379A (en) | 1962-02-19 | 1962-02-19 | Process for producing phenol-modified coumarone-indene type resins |
DEN0021321 | 1962-03-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB946379A true GB946379A (en) | 1964-01-15 |
Family
ID=25988800
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB625762A Expired GB946379A (en) | 1962-02-19 | 1962-02-19 | Process for producing phenol-modified coumarone-indene type resins |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB946379A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0323609A2 (en) * | 1987-12-29 | 1989-07-12 | Nippon Oil Co., Ltd. | Method for preparing light-coloured indene-coumarone resin |
CN112300326A (en) * | 2019-07-26 | 2021-02-02 | 宝武炭材料科技有限公司 | Method for improving hydroxyl value of coumarone resin and application |
CN114057938A (en) * | 2020-08-05 | 2022-02-18 | 宝武炭材料科技有限公司 | Modified liquid coumarone resin and preparation method thereof |
-
1962
- 1962-02-19 GB GB625762A patent/GB946379A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0323609A2 (en) * | 1987-12-29 | 1989-07-12 | Nippon Oil Co., Ltd. | Method for preparing light-coloured indene-coumarone resin |
EP0323609A3 (en) * | 1987-12-29 | 1990-12-12 | Nippon Oil Co., Ltd. | Method for preparing light-coloured indene-coumarone resin |
CN112300326A (en) * | 2019-07-26 | 2021-02-02 | 宝武炭材料科技有限公司 | Method for improving hydroxyl value of coumarone resin and application |
CN114057938A (en) * | 2020-08-05 | 2022-02-18 | 宝武炭材料科技有限公司 | Modified liquid coumarone resin and preparation method thereof |
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