← Back to Patent Explorer
US3197447A Expired / Lapsed US ⏱️ 0.0 years remaining

Polymers and copolymers of acetals of allyl alcohol

Assignee: Nobel Bozel SA
•
Filing: 1961-11-06
•
Granted: 1965-07-27
•
Expires: 1981-11-06
📄 Original PDF 🌐 Google Patents 🔄 Sync Now

Abstract

Abstract The invention comprises compounds of formula: <FORM:0957629/C2/1> where a and b are CH2=CH-CH2-O-, and H, or combined to form O, the compounds being obtained by acetalization of an at least stoichiometric amount of allyl alcohol with glyoxal or glyoxylic acid. The reaction is preferably effected by heating the reactants, a substantial excess of allyl alcohol being used, in the presence of an acid catalyst; whilst removing water by azeotropic distillation. In examples glyoxal-tetra-allylacetal is made from glyoxal and the allylester-diallylacetal of glyoxylic acid from glyoxylic acid, the catalyst being sulphuric acid and the solvent benzene. The products may be polymerized or used as copolymers (see Divisions C3 and D1).ALSO:Compounds of formula: <FORM:0957629/C3/1> where a and b are CH2=CH-CH2-O- and H, or together represent an oxygen radicle, are made by acetalising allyl alcohol with glyoxal or glyoxylic acid, and polymerized or copolymerised. Polymerization or copolymerization may be effected at room temperature, or above, and with or without catalysts. Polymer formation may be carried out in bulk, in solution or in emulsion and oxygen may be present. Control over the extent of polymerisation may be obtained because the allyl radicles take part in the polymerisation successively and any free double bonds remaining after the initial stage may, by more energetic treatment e.g. at a higher temperature or by the use of a catalyst, be cross-linked. Organic peroxides and hydroperoxides are preferred catalysts e.g. tertiary butyl, lauryl, benzoyl and cyclohexanone peroxides, tertiary butyl perbenzoate and tertiary butyl hydroperoxide. Numerous examples are provided of the preparation of various conventional methods, of polymers and copolymers from glyoxal-tetraallylacetal and allyl ester-diallylacetal of glyoxylic acid. Substances used for copolymer formation are ethyl, methyl and butyl acrylates and methacrylates and vinyl acetate and styrene. The products are used in film forming compositions e.g. in paints, varnishes and lacquers. Stoving may be required. Tin tetrachloride and aqueous ammonia and potassium persulphates are other polymerisation catalysts used in the examples the persulphates illustrating preparations by emulsion copolymerisation.ALSO:Cotton fabrics are stiffened by the formation thereon of a polymer or copolymer of a compound of formula <FORM:0957629/D1-D2/1> where a and b are -O-CH2-CH = CH2 and H, or together with the C atom to which they are attached from the C = O radicle. In examples cotton is impregnated with aqueous emulsions comprising, as catalyst, potassium, persulphate, and glyoxal-tetra-allylacetal and 6 sulphonated lauryl alcohol, a condensation product of oleyl alcohol and ethylene oxide, ethyl acrylate and methyl methacrylate and 7 ethyl acrylate, methyl methacrylate and acrylamide, with or without formal, the material being squeezed, dried at 80 DEG C., and stored at 130 DEG C.

Inventors

  • 👤 Talet Pierre

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-29 14:02
CPC Classifications
C; C09; C09D; C09D157/00; C07; C07C; C07C67/00; C07C67/08; C07C69/00; C07C69/66; C07C69/73; C07C69/734; C08; C08F; C08F20/00

Claims Analysis

Total Claims: 2
Claim 1
Independent Claim 17 words
HOMOPOLYMERS PRODUCED BY THE POLYMERIZATION OF A POLYMERIZABLE UNSATURATED MONOMER COMPOUND SELECTED FROM THE GROUP CONSISTING OF:
Claim 2
Dependent Claim 17 words
HOMOPOLYMERS PRODUCED BY THE POLYMERIZATION OF A POLYMERIZABLE UNSATURATED MONOMER COMPOUND SELECTED FROM THE GROUP CONSISTING OF:

References Cited (Backward Citations)

GB510168A Cited
US2409633A Cited
GB599362A Cited
US2561254A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1968-07-26 1969-01-25 1969-07-27 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1972-07-26 1973-01-25 1973-07-27 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1976-07-26 1977-01-25 1977-07-27 $7700.00 Window Closed / Lapsed

Assigned Categories & Tags

No categories assigned to this patent yet.

Assign Category Tag