GB806273A - Production of liquid phenolic condensation products - Google Patents

Production of liquid phenolic condensation products

Info

Publication number
GB806273A
GB806273A GB34285/56A GB3428556A GB806273A GB 806273 A GB806273 A GB 806273A GB 34285/56 A GB34285/56 A GB 34285/56A GB 3428556 A GB3428556 A GB 3428556A GB 806273 A GB806273 A GB 806273A
Authority
GB
United Kingdom
Prior art keywords
water
phenol
reaction mixture
specified
formaldehyde
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
GB34285/56A
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.)
Monsanto Chemicals Ltd
Monsanto Chemical Co
Original Assignee
Monsanto Chemicals Ltd
Monsanto Chemical Co
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 Monsanto Chemicals Ltd, Monsanto Chemical Co filed Critical Monsanto Chemicals Ltd
Publication of GB806273A publication Critical patent/GB806273A/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
    • C08G8/10Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ with phenol

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Phenolic Resins Or Amino Resins (AREA)

Abstract

Light-coloured, stable, water-dilutable, liquid phenolic condensation products are prepared by heating a monohydric phenol, water, 0.8-3 mols. of formaldehyde and/or a substance which acts as a source thereof for each mol. of monohydric phenol and, as a catalyst, lithium or barium oxide, hydroxide or carbonate at a pH not exceeding 9, with the free formaldehyde content of the reaction mixture is less than 5 per cent by weight, cooling the resulting reaction mixture to below 30 DEG C., adjusting the pH of the cooled reaction mixture to 6-7.2 with orthophosphoric acid or a substance which in aqueous solution acts as a source thereof, and thereafter removing separated solids from the reaction mixture. The heating is normally at 30-90 DEG C., water being removed under reduced pressure. Phenols specified include phenol, cresols, xylenols, tertiary butyl phenol, phenethyl phenol and mixtures thereof. There should be sufficient water present to dissolve the phenol(s) and catalyst. Aldehydes specified are formaldehyde, formalin, paraformaldehyde and mixtures thereof. Specified catalysts are lithium hydroxide monohydrate and barium hydroxide octahydrate. Sources of orthophosphoric acid include meta-, hypo- and pyrophosphoric acids. The precipitation proceeds more favourably when the solution contains less than 50 per cent w./w. of the condensation product; to achieve this, water or a water-miscible solvent (e.g. ethanol, isopropanol, butanols with or without small quantities of liquid monocyclic aromatic hydrocarbons such as benzene or xylenes) may be added. The reaction products are dilutable with large quantities of water and may be used as binders for glass fibres and mineral wools, such as rock wool.
GB34285/56A 1955-11-09 1956-11-09 Production of liquid phenolic condensation products Expired GB806273A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US806273XA 1955-11-09 1955-11-09

Publications (1)

Publication Number Publication Date
GB806273A true GB806273A (en) 1958-12-23

Family

ID=22158572

Family Applications (1)

Application Number Title Priority Date Filing Date
GB34285/56A Expired GB806273A (en) 1955-11-09 1956-11-09 Production of liquid phenolic condensation products

Country Status (1)

Country Link
GB (1) GB806273A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4264671A (en) * 1978-08-02 1981-04-28 Weyerhaeuser Company Phenol formaldehyde resoles and laminates
EP0064055A1 (en) * 1980-11-06 1982-11-10 Weyerhaeuser Co Phenol formaldehyde resoles and laminates.
RU2534544C1 (en) * 2013-04-25 2014-11-27 Вячеслав Ефимович Цветков Method of manufacturing phenol-formaldehyde oligomer

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4264671A (en) * 1978-08-02 1981-04-28 Weyerhaeuser Company Phenol formaldehyde resoles and laminates
EP0064055A1 (en) * 1980-11-06 1982-11-10 Weyerhaeuser Co Phenol formaldehyde resoles and laminates.
EP0064055B1 (en) * 1980-11-06 1987-03-04 Weyerhaeuser Company Phenol formaldehyde resoles and laminates
RU2534544C1 (en) * 2013-04-25 2014-11-27 Вячеслав Ефимович Цветков Method of manufacturing phenol-formaldehyde oligomer

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