GB269973A - Improvements in and relating to the manufacture of resin-like bodies - Google Patents

Improvements in and relating to the manufacture of resin-like bodies

Info

Publication number
GB269973A
GB269973A GB236326A GB236326A GB269973A GB 269973 A GB269973 A GB 269973A GB 236326 A GB236326 A GB 236326A GB 236326 A GB236326 A GB 236326A GB 269973 A GB269973 A GB 269973A
Authority
GB
United Kingdom
Prior art keywords
alcohol
reaction
condensing agent
hydrocarbon
resin
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
GB236326A
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.)
Griffiths Bros & Co London Ltd
REGINALD PERCY LEOPOLD BRITTON
Original Assignee
Griffiths Bros & Co London Ltd
REGINALD PERCY LEOPOLD BRITTON
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 Griffiths Bros & Co London Ltd, REGINALD PERCY LEOPOLD BRITTON filed Critical Griffiths Bros & Co London Ltd
Priority to GB236326A priority Critical patent/GB269973A/en
Publication of GB269973A publication Critical patent/GB269973A/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
    • C08G16/00Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00
    • C08G16/02Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes
    • 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
    • C08G10/00Condensation polymers of aldehydes or ketones with aromatic hydrocarbons or halogenated aromatic hydrocarbons only
    • C08G10/02Condensation polymers of aldehydes or ketones with aromatic hydrocarbons or halogenated aromatic hydrocarbons only of aldehydes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Compounds Of Unknown Constitution (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)

Abstract

269,973. Griffiths Bros. & Co., London, Ltd., and Britton, R. P. L. Jan. 27, 1926. Polymerization or condensation products of aromatic alcohols; condensation products of formaldehyde and aromatic hydrocarbons.-Resinous bodies soluble in organic solvents are obtained by treating monohydric aromatic side-chain alcohols with condensing agents. The condensing agents, such as sulphuric or phosphoric acid or phosphorus pentoxide, may be used singly or in combination, and are preferably taken in such amount that at least one-fifth of a molecule is present for each molecule of alcohol. The initial stages of the reaction are generally carried out at a temperature not higher than 180‹ C., but the temperature may be raised later to about 180‹ C. to regenerate the condensing agent. The reaction may be carried out under pressure. The alcohol may be produced in situ by reaction between an aromatic hydrocarbon and formaldehyde, or a substance giving rise thereto. In this modification only phosphoric acid or phosphorus pentoxide is used as condensing agent, and the preferred reaction mixture comprises one molecule of condensing agent and five molecules each of hydrocarbon aud formaldehyde; the reaction mixture is preferably maintained in an emulsified condition by agitation. The alcohol or the hydrocarbon giving rise thereto may contain substituents other than hydroxy groups, such as halogen, in the nucleus. The reaction may be carried out in presence or absence of a solvent, such as an excess of hydrocarbon, and the alcohol or its generators may be added in stages to the condensing agent, the latter being regenerated as required between the additions. The products may be purified by dissolving them in an organic solvent and centrifuging the solution, with or without the addition of a little alkali, and if the solvent is volatile in steam the solution may be steam-distilled. Alternatively, the reaction mass may be treated with water and the resin separated and treated with steam, or the resin may be dissolved in a fused hydrocarbon, such as naphthalene, with or without addition of water, and the solution, after evaporation of the acid layer treated to recover the resin. Alternatively, the reaction mass may be treated with steam at super-atmospheric pressure and the resinous layer separated. In any event, the resin may be further purified by treatment with alkali particularly by fusion with lime. Examples describe the condensation of benzyl alcohol with the use of sulphuric acid as condensing agent, the condensation of cinnamic alcohol with the use in turn of phosphoric acid and sulphuric acid as condensing agents, and the condensation of naphthalene and paraformaldehyde with the use as condensing agent of dehydrated phosphoric acid. The products may be dissolved in organic solvents and used as varnishes or paint excipients. Specification 16245/07, [Class 2, Acids and salts, Organic &c.], is referred to.
GB236326A 1926-01-27 1926-01-27 Improvements in and relating to the manufacture of resin-like bodies Expired GB269973A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB236326A GB269973A (en) 1926-01-27 1926-01-27 Improvements in and relating to the manufacture of resin-like bodies

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB236326A GB269973A (en) 1926-01-27 1926-01-27 Improvements in and relating to the manufacture of resin-like bodies

Publications (1)

Publication Number Publication Date
GB269973A true GB269973A (en) 1927-04-27

Family

ID=9738223

Family Applications (1)

Application Number Title Priority Date Filing Date
GB236326A Expired GB269973A (en) 1926-01-27 1926-01-27 Improvements in and relating to the manufacture of resin-like bodies

Country Status (1)

Country Link
GB (1) GB269973A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3321531A (en) * 1961-09-19 1967-05-23 Haszeldine Robert Neville Fluorinated benzyl ether polymers and process for their preparation

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3321531A (en) * 1961-09-19 1967-05-23 Haszeldine Robert Neville Fluorinated benzyl ether polymers and process for their preparation

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