GB359047A - Improvements in or relating to phenol-furfural resins - Google Patents
Improvements in or relating to phenol-furfural resinsInfo
- Publication number
- GB359047A GB359047A GB2183130A GB2183130A GB359047A GB 359047 A GB359047 A GB 359047A GB 2183130 A GB2183130 A GB 2183130A GB 2183130 A GB2183130 A GB 2183130A GB 359047 A GB359047 A GB 359047A
- Authority
- GB
- United Kingdom
- Prior art keywords
- phenol
- furfural
- hexamethylenetetramine
- wholly
- lime
- 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
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
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)
- Phenolic Resins Or Amino Resins (AREA)
Abstract
Resinous condensation products are manufactured by condensing a phenol with furfural in proportion to yield a reactive resin and incorporating therewith an accelerator comprising an alkaline-earth metal oxide and a methylene containing body, the latter being present in a proportion of the order of 2 per cent of the original reaction mixture. In this manner the time required for hardening is greatly reduced. In an example, furfural is condensed with cresol or phenol and lime and hexamethylenetetramine are added. The lime may be wholly or partially replaced by magnesia and the hexamethylenetetramine wholly or partially by paraformaldehyde. Specifications 187,480, 243,470, and 326,884, [all in Class 2 (iii), Dyes &c.], are referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2183130A GB359047A (en) | 1930-07-18 | 1930-07-18 | Improvements in or relating to phenol-furfural resins |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2183130A GB359047A (en) | 1930-07-18 | 1930-07-18 | Improvements in or relating to phenol-furfural resins |
Publications (1)
Publication Number | Publication Date |
---|---|
GB359047A true GB359047A (en) | 1931-10-19 |
Family
ID=10169536
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2183130A Expired GB359047A (en) | 1930-07-18 | 1930-07-18 | Improvements in or relating to phenol-furfural resins |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB359047A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2745816A (en) * | 1950-12-22 | 1956-05-15 | Hartford Nat Bank & Trust Co | Novolak from phenol and furfural reacted in alkaline medium |
-
1930
- 1930-07-18 GB GB2183130A patent/GB359047A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2745816A (en) * | 1950-12-22 | 1956-05-15 | Hartford Nat Bank & Trust Co | Novolak from phenol and furfural reacted in alkaline medium |
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