GB1068586A - Flexible phenolic baking resins - Google Patents

Flexible phenolic baking resins

Info

Publication number
GB1068586A
GB1068586A GB4738763A GB4738763A GB1068586A GB 1068586 A GB1068586 A GB 1068586A GB 4738763 A GB4738763 A GB 4738763A GB 4738763 A GB4738763 A GB 4738763A GB 1068586 A GB1068586 A GB 1068586A
Authority
GB
United Kingdom
Prior art keywords
bisphenol
mole
reacting
reaction product
catalyst
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
GB4738763A
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.)
Union Carbide Corp
Original Assignee
Union Carbide Corp
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 Union Carbide Corp filed Critical Union Carbide Corp
Publication of GB1068586A publication Critical patent/GB1068586A/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
    • C08G8/28Chemically modified polycondensates
    • 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)
  • General Chemical & Material Sciences (AREA)
  • Paints Or Removers (AREA)

Abstract

A curable phenolic resin composition comprises the reaction product of (a) a polyhydric compound of the formula <FORM:1068586/C3/1> where n is 1 or 2; (b) 10 to 40% by weight of (a) of phenol; and (c) at least one mole of formaldehyde per mole of phenolic OH in (a) and (b) in solution in a solvent volatile at the curing temperature. Reactant (a) may be obtained by reacting 2 moles of bisphenol A with one mole of epichlorohydrin or the diglycidyl ether of bisphenol A using an alkaline catalyst. Specified solvents for (c) are glycol ethers and ether-esters, MIK, diacetone alcohol and C1- 6 alkyl alcohols. Specified catalysts for the reaction include alkali and alkaline earth metal hydroxides, ammonium and tetraalkylammonium hydroxides, tertiary amines, hexamine and sodium amide. Acids may be added to the reaction product to accelerate curing e.g. phosphoric, sulphuric, hydrochloric, oxalic, citric or acetic. In the example (a) is obtained by reacting an epoxy material of epoxide equivalent 185 to 200 and M.W. 350 to 400, consisting predominantly of bisphenol A diglycidyl ether, with bisphenol A using lithium naphthenate as catalyst. The composition is used to coat steel panels by dipping and baking and may be employed as an internal coating for metal containers.ALSO:A curable phenolic resin coating composition comprises the reaction product of (a) a polyhydric compound of formula <FORM:1068586/B1-B2/1> where n is 1 or 2 (b) 10 to 40% by wt. of (a) of phenol, and (c) at least one mole of formaldehyde per mole of phenolic OH in (a) + (b) in solution in a solvent volatile at the curing temperature. Reactant (a) may be obtained by reacting 2 moles bisphenol A with 1 mole of its diglycidyl ether or epichlorohydrin. The composition may be used as an internal coating for metal containers and in the Example is applied to steel panels by dipping and baking at 400 DEG F. An alkaline catalyst may be used for the reaction and an acid catalyst for curing.
GB4738763A 1962-12-24 1963-12-02 Flexible phenolic baking resins Expired GB1068586A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US24666562A 1962-12-24 1962-12-24

Publications (1)

Publication Number Publication Date
GB1068586A true GB1068586A (en) 1967-05-10

Family

ID=22931665

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4738763A Expired GB1068586A (en) 1962-12-24 1963-12-02 Flexible phenolic baking resins

Country Status (1)

Country Link
GB (1) GB1068586A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112430297A (en) * 2020-11-23 2021-03-02 山东仁丰特种材料股份有限公司 Preparation process of carbon paper for phenolic resin modified toughened and reinforced gas diffusion layer

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112430297A (en) * 2020-11-23 2021-03-02 山东仁丰特种材料股份有限公司 Preparation process of carbon paper for phenolic resin modified toughened and reinforced gas diffusion layer

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