GB365093A - The manufacture and use of new synthetic resins - Google Patents

The manufacture and use of new synthetic resins

Info

Publication number
GB365093A
GB365093A GB30842/30A GB3084230A GB365093A GB 365093 A GB365093 A GB 365093A GB 30842/30 A GB30842/30 A GB 30842/30A GB 3084230 A GB3084230 A GB 3084230A GB 365093 A GB365093 A GB 365093A
Authority
GB
United Kingdom
Prior art keywords
cresol
alcohol
allyl
cellulose
acetate
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
GB30842/30A
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.)
Acordis UK Ltd
Original Assignee
British Celanese 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 British Celanese Ltd filed Critical British Celanese Ltd
Publication of GB365093A publication Critical patent/GB365093A/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
    • C08G65/00Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/34Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
    • C08G65/38Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols
    • C08G65/40Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols (I) and other compounds (II), e.g. OH-Ar-OH + X-Ar-X, where X is halogen atom, i.e. leaving group

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)

Abstract

Lacquers, varnishes, and coating compositions are prepared by incorporating a phenol-allyl resin with a cellulose derivative, with or without the addition of solvents, plasticizers, softeners, other resins, fire retardants, &c. The resins are obtained by condensing a phenolic body, such as phenol, a cresol or xylenol, with allyl alcohol, its esters both organic and inorganic, e.g. the acetate, bromide or iodide, and its ethers, e.g. allyl ethyl ether and diallyl ether, preferably in the presence of a catalyst. The cellulose derivative may comprise the nitrate, acetate, formate, propionate, butyrate or other ester, or ethyl-cellulose, methyl-cellulose, benzyl-cellulose, or other ether. Of the solvents which may be used are mentioned acetone, alcohol, benzene, ethylene dichloride, ethyl acetate, ethyl lactate, tetrachlorethane, and diacetone-alcohol. As examples of plasticizers, reference is made to diphenylolpropane, triacetin, dibutyl tartrate, diethyl phthalate, and xylene monomethylsulphonamide. Other resins mentioned are the artificial resins from phenol-formaldehyde and diphenylolpropane-formaldehyde, or the natural resins manila, acaroid, pontianak, kauri, dammar, rosin, shellac and ester gums. Brominated aromatic compounds, e.g. brominated tricresyl phosphate, may be present as fire retardants. Examples are given of the preparation of (1) coating compositions consisting of (a) cellulose acetate, cresol-allyl resin and acetone, (b) cellulose acetate, cresol-allyl resin, acetone, benzene, alcohol, and diacetone-alcohol, (c) cellulose nitrate, camphor, diethyl phthalate, cresol-allyl resin, benzene, alcohol, butyl alcohol, butyl and ethyl acetates; (2) a lacquer consisting of cellulose acetate, cresolallyl resin, diphenylolpropane, pigment, acetone, ethyl acetate and lactate, benzene and toluene. In each case the cresol-allyl resin is prepared by condensing cresol with allyl alcohol or an allyl ester or ether.ALSO:Lacquers, varnishes, coating compositions, plastic materials, adhesives, filaments, and photographic and other films are prepared by incorporating a phenol-allyl resin with a cellulose derivative, with or without the addition of solvents, plasticizers, softeners, other resins, fire retardants, &c. The resins are obtained by condensing a phenolic body, such as phenol, a cresol or xylenol, with allyl alcohol, its esters both organic and inorganic e.g. the acetate, bromide, or iodide and its ethers, e.g. allyl ethyl ether and diallyl ether, preferably in the presence of a catalyst. Examples are given of the condensation of o-cresol with allyl alcohol and allyl iodide in the presence of zinc chloride, and of o-cresol with allyl acetate using ferric chloride as catalyst. The cellulose derivative may comprise the nitrate, acetate, formate, propionate, butyrate or other ester, or ethyl-cellulose, methyl-cellulose, benzyl-cellulose or other ether. Of the solvents which may be used are mentioned acetone, alcohol, benzene, ethylene dichloride, ethyl acetate, ethyl lactate, tetrachlorethane and diacetone-alcohol. As examples of plasticizers, reference is made to diphenylolpropane, triacetin, dibutyl tartrate, diethyl phthalate and xylene monomethylsulphonamide. Other resins mentioned are the artificial resins from phenol-formaldehyde and diphenylolpropane-formaldehyde, or the natural resins manila, acaroid, pontianak, kauri, dammar, rosin, shellac and ester gums. Brominated aromatic compounds, e.g. brominated tricresyl phosphate, may be present as fire-retardants. Solutions containing a phenol-allyl resin and a cellulose derivative may be used as lacquers for coating metal, glass, &c., or for the production of filaments by wet or dry spinning methods. Plastic materials containing a cellulose derivative and a phenol-allyl resin may be made into sheets of reinforcing material for reinforced glass, whilst a solution containing the resin may be used as an adhesive, especially for securing cellulose derivative sheets to sheets of glass in the manufacture of reinforced glass. Examples are given of the preparation of (1) coating compositions consisting of (a) cellulose acetate, cresol-allyl resin and acetone, (b) cellulose acetate, cresol-allyl resin, acetone, benzene, alcohol and diacetone-alcohol, (c) cellulose nitrate, camphor, diethyl phthalate, cresol-allyl resin, benzene, alcohol, butyl alcohol, butyl and ethyl acetates; (2) adhesives, specially suitable for securing sheets of material having a basis of a cellulose derivative to surfaces of glass, cardboard, asbestos, metal, comprising (a) cellulose acetate, cresol-allyl resin, acetone, ethyl acetate and lactate, (b) cellulose nitrate, camphor, dibutyl phthalate, cresol-allyl resin, benzene, alcohol, butyl alcohol and acetate, and ethyl acetate; (3) a plastic composition consisting of cellulose acetate, cresol-allyl resin, xylene monomethyl-sulphonamide, alcohol and benzene; (4) a solution for making filaments by dry spinning methods containing cellulose acetate, cresol-allyl resin and acetone; (5) a lacquer consisting of cellulose acetate, cresol-allyl resin, diphenylolpropane, pigment, acetone, ethyl acetate and lactate, benzene and toluene. In each case the cresol-allyl resin is prepared by condensing cresol with allyl alcohol or an allyl ester or ether.ALSO:Plastic materials and adhesives are prepared by incorporating a phenol-allyl resin with a cellulose derivative, with or without the addition of solvents, plasticizers, softeners, other resins, fire retardants, &c. The resins are obtained by condensing a phenolic body, such as phenol, a cresol or xylenol, with allyl alcohol, its esters both organic and inorganic, e.g. the acetate, bromide or iodide, and its ethers, e.g. allyl ethyl ether and diallyl ether, preferably in the presence of a catalyst. For use as an adhesive, a solution of the resin alone may be employed. The cellulose derivative may comprise the nitrate, acetate, formate, propionate, butyrate, or other ester, or ethyl-cellulose, methyl-cellulose, benzyl-cellulose, or other ether. Of the solvents which may be used are mentioned acetone, alcohol, benzene, ethylene dichloride, ethyl acetate, ethyl lactate, tetrachlorethane, and diacetone-alcohol. As examples of plasticizers, reference is made to diphenylolpropane, triacetin, dibutyl tartrate, diethyl phthalate, and xylene monomethylsulphonamide. Other resins mentioned are the artificial resins from phenol-formaldehyde and diphenylolpropane-formaldehyde, or the natural resins manila, acaroid, pontianak, kauri, dammar, rosin, shellac, and ester gums. Brominated aromatic compounds, e.g. brominated tricresyl phosphate, may be present as fire retardants. Adhesives, specially suitable for securing sheets of material having a basis of a cellulose derivative to surfaces of glass, cardboard, asbestos, metal, consist of (a) cellulose acetate, cresol-allyl resin, acetone, ethyl acetate, and lactate, or (b) cellulose nitrate, camphor, dibutyl phthalate, cresol-allyl resin, benzene, alcohol, butyl alcohol and acetate, and ethyl acetate. A plastic composition consists of cellulose acetate, cresol-allyl resin, xylene monomethylsulphonamide, alcohol, and benzene. In each case the cresol-allyl resin is prepared by condensing cresol with allyl alcohol or an allyl ether or ester.
GB30842/30A 1929-10-15 1930-10-15 The manufacture and use of new synthetic resins Expired GB365093A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US365093XA 1929-10-15 1929-10-15

Publications (1)

Publication Number Publication Date
GB365093A true GB365093A (en) 1932-01-15

Family

ID=21888977

Family Applications (1)

Application Number Title Priority Date Filing Date
GB30842/30A Expired GB365093A (en) 1929-10-15 1930-10-15 The manufacture and use of new synthetic resins

Country Status (1)

Country Link
GB (1) GB365093A (en)

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