GB550925A - Improvements in or relating to condensation products of formaldehyde and monomeric compounds - Google Patents

Improvements in or relating to condensation products of formaldehyde and monomeric compounds

Info

Publication number
GB550925A
GB550925A GB9452/41A GB945241A GB550925A GB 550925 A GB550925 A GB 550925A GB 9452/41 A GB9452/41 A GB 9452/41A GB 945241 A GB945241 A GB 945241A GB 550925 A GB550925 A GB 550925A
Authority
GB
United Kingdom
Prior art keywords
formaldehyde
urea
parts
sulphonamide
acid
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
GB9452/41A
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of GB550925A publication Critical patent/GB550925A/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
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/54Polycondensates 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)

Abstract

550,925. Synthetic recess modified with polyisocyanate. DU PONT DE NEMOURS & CO., E. I. July 25, 1941, No. 9452. Convention date, July 25, 1940. [Class 2 (iii)] Modified phenol-formaldehyde, urea-formaldehyde and sulphonamide-formaldehyde resinous condensation products are obtained by carrying out the condensation reaction in the presence of a polyisocyanate or thioisocyanate. Resinous condensation of the following bodies with formaldehyde may be thus given improved baking characteristics and water resistance-ohydroxy-benzyl alcohol, o-cresol, m-cresol, p-cresol, p-phenylphenol, xylenols, diphenylol propane, resorcinol, urea, guanidine, monomethylolurea, acetyl urea, phenyl urea, methyl urea, thiourea, o, m, and p-toluenesulphonamide tetrahydronaphthalenesulphonamide, adipamide. Pigments, mica, whiting, alumina, synthetic or natural resins (rosins, ester gums, copal, kauri, congo, manilla, damar, shellac), ), drying &c. oils, waxes, (carnauba, beeswax, paraffin, spermaceti, montan) inhibitors (pine oil, hydroquininone, guaiacol, creosote, soya lecithin (mineral oils may be mixed with the reacting materials. In examples (1) 100 parts p-phenylphenol formaldehyde resin ("Bakelite" XR 254) dissolved in 100 parts toluene are mixed with 9 parts hexamethylene diisocyanate and 0.1 parts benzoyl peroxide. A film of the mixture baked for one hour at 100‹C. gives a product of improved hardness, (3) a urea-formaldehyde resin prepared by heating one part dimethylolurea and 2 parts isobutanol in presence of phthalic acid while eliminating water is dissolved in dioxane and the solution mixed with a xylene solution of a castor oil modified glyceryl phthalate resin and with 5 parts hexamethylene diisocyanate, a film of the mixture being baked for one hour at 127‹C. Specifications 547,672 and 548,807 are referred to. The Specification as open to inspection under Sect. 91 includes the modification by isocyanates of the resinous condensation products of the following substances with formaldehyde-anisole, α and #-naphthol ethyl ether, diphenyl ether α-naphthol, #-naphthol, methyl and ethyl ethers of 1:3:5 xylenol, salicylic acid, o-methoxybenzoic acid, ethyl salicylate, phenoxy acetic acid, glycol monophenyl ethers, diphenylol cyclohexane, dithiophenylol propane, thiophenol, thiocresol, monochlorophenol, catechol, pyrogallol, formamide, acetamide, naphthalene, anthracene, phenanthrene, acenaphthene, chloronaphthalene, #-naphthalene sulphonic acid, acetone, cyclohexanone, cyclopentanone, naphthalene sulphonamide, chlorobenzene sulphonamide, nitrobenzene sulphonamide, aniline, o-toluedine, α and #-naphthylamine, benzylaniline, urethane, hexamethylene diurea, salicyl aldehyde and acetaldehyde. This subjectmatter does not appear in the Specification as accepted.
GB9452/41A 1940-07-25 1941-07-25 Improvements in or relating to condensation products of formaldehyde and monomeric compounds Expired GB550925A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US550925XA 1940-07-25 1940-07-25

Publications (1)

Publication Number Publication Date
GB550925A true GB550925A (en) 1943-02-01

Family

ID=21995537

Family Applications (1)

Application Number Title Priority Date Filing Date
GB9452/41A Expired GB550925A (en) 1940-07-25 1941-07-25 Improvements in or relating to condensation products of formaldehyde and monomeric compounds

Country Status (1)

Country Link
GB (1) GB550925A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2475347A (en) * 1944-09-09 1949-07-05 Du Pont Polymers from nitropolyhydroxy alcohols and polyamines
WO1979000223A1 (en) * 1977-10-21 1979-05-03 A Ehrensperger Manufacturing process of shaped models and devices
US10947382B2 (en) 2016-09-28 2021-03-16 Shpp Global Technologies B.V. Phenylene ether copolymer and compositions comprising same

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2475347A (en) * 1944-09-09 1949-07-05 Du Pont Polymers from nitropolyhydroxy alcohols and polyamines
WO1979000223A1 (en) * 1977-10-21 1979-05-03 A Ehrensperger Manufacturing process of shaped models and devices
US10947382B2 (en) 2016-09-28 2021-03-16 Shpp Global Technologies B.V. Phenylene ether copolymer and compositions comprising same

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