GB483987A - Improvements in the production of synthetic resins and the manufacture of films or sheets therefrom - Google Patents

Improvements in the production of synthetic resins and the manufacture of films or sheets therefrom

Info

Publication number
GB483987A
GB483987A GB20470/36A GB2047036A GB483987A GB 483987 A GB483987 A GB 483987A GB 20470/36 A GB20470/36 A GB 20470/36A GB 2047036 A GB2047036 A GB 2047036A GB 483987 A GB483987 A GB 483987A
Authority
GB
United Kingdom
Prior art keywords
per cent
polyvinyl
vinyl
acetaldehyde
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
GB20470/36A
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.)
Kodak Ltd
Original Assignee
Kodak 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 Kodak Ltd filed Critical Kodak Ltd
Publication of GB483987A publication Critical patent/GB483987A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment
    • C08F8/28Condensation with aldehydes or ketones
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S215/00Bottles and jars
    • Y10S215/02Coatings and laminations for making of bottle caps

Landscapes

  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

Polyvinyl acetal resins are prepared by reacting a polyvinyl ester at a temperature not above 50 DEG C. with one or more aliphatic aldehydes boiling below 100 DEG C. (other than formaldehyde) in the presence of a de-esterifying agent and of a strong acid catalyst in a quantity from 1-5 per cent of the reactants and not more than 10 per cent of the polyvinyl ester. The aldehydes may be used in monomeric or polymeric form, or there may be used substances which yield them, e.g. paraldehyde or acetaldehyde diethylacetal. In modifications, if the aldehyde present be in 50-200 per cent excess, or if the reactants be dispersed in a medium consisting substantially entirely of one or more alcohols, the quantity of catalyst may be increased up to 20 per cent of the polyvinyl ester; or the reaction is carried out with the addition of formaldehyde, aliphatic aldehydes boiling above 100 DEG C., cyclic aldehydes, cyclic ketones (e.g. cyclohexanone), or mixtures thereof, in such quantity that the acetal portion of the product contains not more than 25 per cent (mols.) of acetal derived therefrom, the catalyst in this case also being present up to 20 per cent of the polyvinyl ester. The reaction is preferably carried out with polyvinyl acetate, and at 35-40 DEG C. Starting materials specified are: aliphatic aldehydes boiling below 100 DEG C.-acetaldehyde, propionaldehyde, butyraldehyde; de-esterifying agents-methyl, ethyl, propyl and iso-propyl alcohols or ethylene glycol, with or without additional solvents such as methyl or ethyl acetate, dibutyl ether, heptane, ethylene dichloride, benzene, nitroethane; catalysts-sulphuric, alkyl sulphuric and sulphonic, trichloracetic, hydrochloric acids. The resins may be made into photographic-film bases by pressing into blocks and skiving or by coating a solution (e.g. in acetone, ethyl, alcohol, ethylene dichloride, or mixtures thereof) on to a glass or metal plate or a revolving drum, stripping, and curing by heating with warm air. Examples illustrate the preparation of resins from polyvinyl acetate and acetaldehyde, butyraldehyde, or acetaldehyde and (a) butyraldehyde, (b) benzaldehyde, or (c) cyclohexanone, under various conditions. Specification 477,446 is referred to. The Provisional Specification refers to the use of polyvinyl formate, propionate, butyrate, interpolymers of vinyl acetate with vinyl propionate, vinyl oleate, vinyl chloride, vinyl ethyl ether, and styrene, and states broadly that the quantity of catalyst does not exceed 20 per cent of the polyvinyl ester.
GB20470/36A 1936-06-17 1936-07-23 Improvements in the production of synthetic resins and the manufacture of films or sheets therefrom Expired GB483987A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US85733A US2129450A (en) 1936-06-17 1936-06-17 Polyvinyl acetal resin

Publications (1)

Publication Number Publication Date
GB483987A true GB483987A (en) 1938-04-25

Family

ID=22193580

Family Applications (1)

Application Number Title Priority Date Filing Date
GB20470/36A Expired GB483987A (en) 1936-06-17 1936-07-23 Improvements in the production of synthetic resins and the manufacture of films or sheets therefrom

Country Status (3)

Country Link
US (1) US2129450A (en)
FR (1) FR830746A (en)
GB (1) GB483987A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2200119A (en) * 1984-01-04 1988-07-27 Ulano Corp Hardener composition for polymer films

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2475002A (en) * 1943-04-30 1949-07-05 Bell Telephone Labor Inc Stabilization of cured polymers
US2513189A (en) * 1947-01-18 1950-06-27 Du Pont Preparation of polyvinyl acetals
US2828289A (en) * 1955-03-09 1958-03-25 Eastman Kodak Co Polyvinyl acetal acid dicarboxylates and their preparation
FR1313064A (en) * 1959-05-13 1962-12-28 Inst Francais Du Petrole New high polymer coloring process
BE615938A (en) * 1961-04-05
US4335036A (en) * 1980-05-30 1982-06-15 E. I. Du Pont De Nemours And Company Plasticized polyvinyl butyral employing propylene oxide oligomers

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2200119A (en) * 1984-01-04 1988-07-27 Ulano Corp Hardener composition for polymer films
GB2200119B (en) * 1984-01-04 1991-01-30 Ulano Corp Hardener composition

Also Published As

Publication number Publication date
FR830746A (en) 1938-08-05
US2129450A (en) 1938-09-06

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