GB1044149A - Silane-modified novolac resins - Google Patents
Silane-modified novolac resinsInfo
- Publication number
- GB1044149A GB1044149A GB3101465A GB3101465A GB1044149A GB 1044149 A GB1044149 A GB 1044149A GB 3101465 A GB3101465 A GB 3101465A GB 3101465 A GB3101465 A GB 3101465A GB 1044149 A GB1044149 A GB 1044149A
- Authority
- GB
- United Kingdom
- Prior art keywords
- reaction
- products
- alkyl
- paper
- aromatic hydrocarbon
- 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
- C08G8/28—Chemically modified polycondensates
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)
- Adhesives Or Adhesive Processes (AREA)
- Phenolic Resins Or Amino Resins (AREA)
Abstract
Soluble fusible reaction products result from the reaction of (1) a novolac of recurring structural units <PICT:1044149/C3/1> where A is an aromatic hydrocarbon nucleus, R is alkylidene ortho to the OH of both A nuclei to which it is attached, R1 is an alkyl or aromatic hydrocarbon radical para to the OH, and n is 0 or 1; with (2) a dihalosilane, (1) may be obtained by standard novolac procedures from a p-alkyl or p-aryl phenol when n is 1, or from a p-halophenol followed by replacement of Ha by H, when n is 0, and an aldehyde e.g. formaldehyde, acetaldehyde, butyraldehyde or benzaldehyde. Reaction may be effected in an inert solvent over a wide temperature range in the presence of an acid acceptor e.g. a tertiary amine. The products may be cross-linked by heating with an alkali metal or its hydroxide, carbonate, alkoxide or aryloxide or a quaternary ammonium salt as catalyst. The products may be used in coatings and impregnants for paper, textiles and leather; in paints, varnishes, adhesives and rubber; as moulding compounds with fillers e.g. wood flour, cotton flock or glass fibres; and when thermoset as binders for sand, asbestos, silicon carbide or paper.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US24113162A | 1962-11-30 | 1962-11-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1044149A true GB1044149A (en) | 1966-09-28 |
Family
ID=22909392
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3101465A Expired GB1044149A (en) | 1962-11-30 | 1963-11-05 | Silane-modified novolac resins |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1044149A (en) |
-
1963
- 1963-11-05 GB GB3101465A patent/GB1044149A/en not_active Expired
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