GB327722A - Improvements in the manufacture and production of condensation products - Google Patents

Improvements in the manufacture and production of condensation products

Info

Publication number
GB327722A
GB327722A GB36397/28A GB3639728A GB327722A GB 327722 A GB327722 A GB 327722A GB 36397/28 A GB36397/28 A GB 36397/28A GB 3639728 A GB3639728 A GB 3639728A GB 327722 A GB327722 A GB 327722A
Authority
GB
United Kingdom
Prior art keywords
acids
esters
products
linseed
phthalic
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
GB36397/28A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
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
Priority to DEI35554D priority Critical patent/DE534215C/en
Priority claimed from DEI35554D external-priority patent/DE534215C/en
Application filed by IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to GB36397/28A priority patent/GB327722A/en
Priority to FR685565D priority patent/FR685565A/en
Publication of GB327722A publication Critical patent/GB327722A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D167/00Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
    • 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
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/66Polyesters containing oxygen in the form of ether groups
    • C08G63/668Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds
    • 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
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/68Polyesters containing atoms other than carbon, hydrogen and oxygen
    • C08G63/688Polyesters containing atoms other than carbon, hydrogen and oxygen containing sulfur
    • C08G63/6884Polyesters containing atoms other than carbon, hydrogen and oxygen containing sulfur derived from polycarboxylic acids and polyhydroxy compounds
    • 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
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/78Preparation processes
    • C08G63/82Preparation processes characterised by the catalyst used
    • C08G63/83Alkali metals, alkaline earth metals, beryllium, magnesium, copper, silver, gold, zinc, cadmium, mercury, manganese, or compounds thereof

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Paints Or Removers (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)
  • Heat Sensitive Colour Forming Recording (AREA)

Abstract

327,722. Johnson, J. Y., (I. G. Farbenindustrie Akt.-Ges.). Dec. 10, 1928. Band.-Synthetic resins are prepared by reacting ether or thio-ether dicarboxylic acids or their anhydrides with polyhydric alcohols (including ether-alcohols such as polyglycols and polyglycerols containing at least two hydroxy groups) or esters of polyhydric alcohols with fatty acids, such as oleic, elaeostearic, or the acids of linseed or China-wood oil, or the hydroxy alkyl esters of higher fatty acids which may be obtained by the reaction of olefine oxides or halogen hydrins on the corresponding acids, the esters in all cases containing at least one free hydroxy group. The dicarboxylic acids mentioned are diglycollic, methyl-diglycollic, dihydracrylic, salicyl-acetic, thiodiglycollic, thiodilactylic, and 2-carboxyphenyl thioglycollic acids. A part of the dicarboxylic acid may be replaced by phthalic, succinic, adipic or like dicarboxylic acid. The reaction mixture may contain higher fatty acids such as oleic or elaeostearic acids or the acids of linseed or China wood oil. The reaction may be effected with exclusion of oxygen, for instance in a current of inert gas or in vacuo or under pressure and with or without condensing agents such as metals, metal oxides, acids, acid or alkaline substances, sodium acetate, and zinc chloride, and with or without diluents or solvents such as phthalic esters, butyl diglycollates, glycol diacetate natural or artificial resins such as colophony or phenolformaldehyde condensation products. The products are suitable for the production of lacquers, films, insulating materials and many other articles, and various additions, such as ketones, alcohols, acetic esters, softening agents such as phthalic or phosphoric aesters, oils such as linseed and China-wood oil, waxes, fillers, and colouring matters may be added, at any stage before the final hardening for stance during the condensation process. Asbestos, slate-meal, talc, mica, alumina, slag-powder, lime and gypsum are mentioned as suitable fillers. The products may be used as substitutes for marble, slate, and ceramic products, for brake bands, grinding tools, &c. Specification 328,190, [Class 2 (iii), Dyes, &c.], is referred to.
GB36397/28A 1928-09-18 1928-12-10 Improvements in the manufacture and production of condensation products Expired GB327722A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
DEI35554D DE534215C (en) 1928-09-18 1928-09-19 Process for the production of condensation products
GB36397/28A GB327722A (en) 1928-09-19 1928-12-10 Improvements in the manufacture and production of condensation products
FR685565D FR685565A (en) 1928-09-18 1929-09-02 Process for obtaining condensation products

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DEI35554D DE534215C (en) 1928-09-18 1928-09-19 Process for the production of condensation products
GB36397/28A GB327722A (en) 1928-09-19 1928-12-10 Improvements in the manufacture and production of condensation products

Publications (1)

Publication Number Publication Date
GB327722A true GB327722A (en) 1930-04-10

Family

ID=25981524

Family Applications (1)

Application Number Title Priority Date Filing Date
GB36397/28A Expired GB327722A (en) 1928-09-18 1928-12-10 Improvements in the manufacture and production of condensation products

Country Status (1)

Country Link
GB (1) GB327722A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2518245A (en) * 1946-08-24 1950-08-08 Shell Dev Process for preparing copolymers from alkylene glycols and di(hydroxyalkyl) sulfides

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2518245A (en) * 1946-08-24 1950-08-08 Shell Dev Process for preparing copolymers from alkylene glycols and di(hydroxyalkyl) sulfides

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