GB576745A - Improvements in or relating to resinous compositions - Google Patents

Improvements in or relating to resinous compositions

Info

Publication number
GB576745A
GB576745A GB3786/44A GB378644A GB576745A GB 576745 A GB576745 A GB 576745A GB 3786/44 A GB3786/44 A GB 3786/44A GB 378644 A GB378644 A GB 378644A GB 576745 A GB576745 A GB 576745A
Authority
GB
United Kingdom
Prior art keywords
formaldehyde
phenol
resin
resorcinol
per cent
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
Application number
GB3786/44A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bakelite Ltd
Original Assignee
Bakelite Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Bakelite Ltd filed Critical Bakelite Ltd
Publication of GB576745A publication Critical patent/GB576745A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G8/00Condensation polymers of aldehydes or ketones with phenols only
    • C08G8/04Condensation polymers of aldehydes or ketones with phenols only of aldehydes
    • C08G8/08Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ
    • C08G8/24Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ with mixtures of two or more phenols which are not covered by only one of the groups C08G8/10 - C08G8/20

Landscapes

  • 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

Resins are made by heating a monohydric phenol with aqueous formaldehyde in presence of an acid catalyst to form a potentially heat-reactive resin, treating the resin for the removal therefrom or the neutralization therein of the acid, and before or after dehydrating, mixing therewith resorcinol and between 16 and 24 per cent of its weight of formaldehyde, paraformaldehyde or other polymer of formaldehyde (calculated as paraformaldehyde) and heating the mixture to bring it to the brittle stage. The phenol may be, for example, phenol itself, or a cresol, and the acid catalyst may be hydrochloric, sulphuric, or phosphoric acid and may be removed by washing with warm water or by neutralization with barium hydroxide. Preferably, the neutral potentially heat-reactive monohydric phenolic resin is melted after dehydration, the resorcinol is dissolved therein, and the formaldehyde or polymer thereof is added to the solution. The proportion of monohydric phenol resin in the resin should be about 10-90 per cent and preferably 50-80 per cent, and free phenol may be present. The amount of hardening agent, e.g. hexamethylene tetramine, required may vary from 2-10 per cent. The resins are used for moulding compositions, varnishes and adhesives, e.g. for bonding coating materials to walls of tanks, and may be incorporated with elastomers such as rubber or polyvinyl butyral. In examples, a resin obtained from equimolecular proportions of phenol and formaldehyde is: (1), (2) and (3), dehydrated and melted with varying proportions of resorcinol and paraformaldehyde, and (4) mixed with resorcinol and aqueous formaldehyde, followed by dehydration. Reference is made to the mixing of the product of example 1 with wood flour and to its solution in alcohol or acetone.
GB3786/44A 1943-03-04 1944-02-29 Improvements in or relating to resinous compositions Expired GB576745A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US576745XA 1943-03-04 1943-03-04

Publications (1)

Publication Number Publication Date
GB576745A true GB576745A (en) 1946-04-17

Family

ID=22012056

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3786/44A Expired GB576745A (en) 1943-03-04 1944-02-29 Improvements in or relating to resinous compositions

Country Status (1)

Country Link
GB (1) GB576745A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2861971A (en) * 1954-03-23 1958-11-25 Basf Ag Hardenable resinous mixtures containing a halogen hydrin and processes for producingand hardening same
US2954360A (en) * 1951-03-07 1960-09-27 Basf Ag Process for producing oxygen-containing condensation resins from aromatic hydrocarbons and product produced thereby

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2954360A (en) * 1951-03-07 1960-09-27 Basf Ag Process for producing oxygen-containing condensation resins from aromatic hydrocarbons and product produced thereby
US2861971A (en) * 1954-03-23 1958-11-25 Basf Ag Hardenable resinous mixtures containing a halogen hydrin and processes for producingand hardening same

Similar Documents

Publication Publication Date Title
US3227667A (en) Lignin, phenol, and aldehyde condensation process and product
GB1099187A (en) A method of making phenol-resorcinol-formaldehyde resins
US2385372A (en) Production of resin
US1955731A (en) Phenol resin and process of making the same
US2441860A (en) Accelerated curing of phenol-form-aldehyde resins to the infusible state with 3, 5-xyenol
US2432544A (en) Resorcinol-aldehyde combined with aromatic amine-aldehyde resin
US3254038A (en) Adhesive composition comprising phenolic resin, a tannin and an alkali metal hydroxide
GB576745A (en) Improvements in or relating to resinous compositions
US2563614A (en) Phenolic resin and method of making
US3043804A (en) Curing promoter for furane resins
US2264732A (en) Manufacture of proteinaceous phenolic resin
US2414416A (en) Method of setting phenol-aldehyde resins and products derived therefrom
US2163264A (en) Condensation products from formaldehyde and urea
US2965601A (en) Brittle furfurylated phenolic resins and method of making same
GB631109A (en) Improvements in or relating to method of making an artificial thermosetting resin and the improved resin resulting therefrom
SU61204A1 (en) The method of manufacture of plastic moldings
US1632113A (en) Phenolic condensation product
US1793312A (en) Synthetic resin and process of making same
US3226364A (en) Two-part catalyst system in process for preparing one stage phenolic resins
GB604599A (en) Synthetic resin and process of making same
GB664527A (en) Improvements in or relating to heat-hardenable phenol-formaldehyde resinous compositions
SU423818A1 (en) GLUE COMPOSITION
US1720895A (en) Phenolic resin and process of making same
GB583236A (en) Improvements in and relating to phenolic-aldehyde resinous compositions
US3389101A (en) Redwood extract substituted-phenolic resin adhesive