GB914152A - New condensation products and process of preparing them - Google Patents

New condensation products and process of preparing them

Info

Publication number
GB914152A
GB914152A GB1870259A GB1870259A GB914152A GB 914152 A GB914152 A GB 914152A GB 1870259 A GB1870259 A GB 1870259A GB 1870259 A GB1870259 A GB 1870259A GB 914152 A GB914152 A GB 914152A
Authority
GB
United Kingdom
Prior art keywords
groups
polyethylene glycol
glycerine
ammonia
reacted
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
GB1870259A
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.)
Hoechst AG
Original Assignee
Hoechst AG
Farbwerke Hoechst 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
Application filed by Hoechst AG, Farbwerke Hoechst AG filed Critical Hoechst AG
Publication of GB914152A publication Critical patent/GB914152A/en
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/55Epoxy resins
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L63/00Compositions of epoxy resins; Compositions of derivatives of epoxy resins
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/39Aldehyde resins; Ketone resins; Polyacetals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Epoxy Resins (AREA)

Abstract

In a process for improving textile fibrous material, a polyoxyethylene compound containing at least 2 terminal primary amino groups (a) is reacted on the material with a compound containing at least 2 epoxy groups (b), the proportions being such that the condensation product contains at least 50% of polymeric ethylene oxide. Suitable amino compounds (a) are polyethylene glycols in which at least 2 OH groups have been replaced by NH2 groups; hydroxyethylation products of ammonia, of polyhydric alcohols (e.g. triethanolamine, glycerine, butane-diol, trimethylol propane), or of polyvalent amines (e.g. diethylene triamine), having molecular weights of about 300 to 2,500, of which at least 2 terminal OH groups have been converted to NH2 groups; and reaction products of polyepoxides containing polyethylene glycol residues with ammonia or amines. Suitable polyepoxides (b) are glycidyl ethers of polyhydroxy compounds such as ethylene glycol, polyethylene glycol and the corresponding propylene and butylene glycols, glycerine, sorbitol, pentaerythritol, butene-diol, hexadecane-triol, polypropylene oxide, diphenylol-propanedihydroxy ethyl ether, xylylene alcohol, diphenylolpropane and -methane, and cyanuric acid, and butadiene dioxide. A soluble pre-condensate may first be formed before applying to the fibre together with the necessary amount of one of the reactants to effect cross-linking. The reaction components are preferably applied in aqueous solutions, but may be applied separately or together in solution or dispersion in an organic solvent with or without water. Examples of organic solvents are dioxane, benzene, chlorobenzene and chlorinated hydrocarbons of 1-3 carbon atoms. Hardening is effected at temperatures of from 40 DEG to 160 DEG C. Other components such as aldehydes, aminoplast pre-condensates and softeners, fillers &c., may be incorporated. In the Examples, (1) o ,o 1-diamino-polyethylene glycol, prepared by reacting the bis-benzene-sulphonic acid ester of the glycol (mol. weight= 1,000) with ammonia, is reacted with glycerine diglycidyl ether; (2) triglycidyl cyanurate and the glycidyl ether of 4,41-diphenylol propane respectively are reacted with a similar diaminoglycol (mol. weight=1,500); (3) polyethylene glycol-di-(3-amino-2-hydroxypropyl) ether, prepared from bis-glycidyl ether of polyethylene glycol (600) and NH3, is reacted with a mixture of glycerine di- and tri-glycidyl ether.ALSO:In a process for improving the anti-static and pigment fixation properties of textile fibrous material, a polyoxyethylene compound containing at least 2 terminal primary amino groups (a), is reacted on the material with a compound containing at least 2 epoxy groups, (b), the proportions being such that the condensation product contains at least 50% of polymeric ethylene oxide. Suitable amino compounds (a) are polyethylene glycols in which at least 2 OH groups have been replaced by NH2 groups; hydroxyethylation products of ammonia, of polyhydric alcohols (e.g. triethanolamine, glycerine, butane-diol, trimethylol propane), or of polyvalent amines (e.g. diethylene triamine), having molecular weights of about 300 to 2,500, of which at least 2 terminal OH groups have been converted to NH2 groups; and reaction products or polyepoxides containing poly-ethylene glycol residues with ammonia or amines. Suitable polyepoxides (b) are glycidyl ethers of polyhydroxy compounds such as ethylene glycol, polyethylene glycol and the corresponding propylene and butylene glycols, glycerine, sorbitol, pentaerythitol, butanediol, hexadecane-triol, polypropylene oxide, diphenylol-propane-dihydroxyethyl ether, xylylene alcohol, diphenylol-propane and -methane, and cyanuric acid, and butadiene dioxide. A soluble pre-condensate may first be formed before applying to the fibre together with the necessary amount of one of the reactants to effect cross-linking. The reaction components are preferably applied in aqueous solution, but may be applied separately or together in solution or dispersion in an organic solvent with or without water. Examples of organic solvents are dioxane, benzene, chlorobenzene or chlorinated hydro-carbons of 1-3 carbon atoms. Hardening is effected at temperatures of from 40 DEG to 160 DEG C. Other components such as aldehydes, aminoplast pre-condensates and softeners, and fillers may be incorporated. Specified textile fibres are those of polyethylene glycol terephthalate and polycaprolactam.
GB1870259A 1958-05-31 1959-06-01 New condensation products and process of preparing them Expired GB914152A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF25873A DE1131404B (en) 1958-05-31 1958-05-31 Process for the production of water-insoluble, nitrogen-containing condensation products

Publications (1)

Publication Number Publication Date
GB914152A true GB914152A (en) 1962-12-28

Family

ID=7091798

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1870259A Expired GB914152A (en) 1958-05-31 1959-06-01 New condensation products and process of preparing them

Country Status (5)

Country Link
BE (1) BE579238A (en)
DE (1) DE1131404B (en)
FR (1) FR1226159A (en)
GB (1) GB914152A (en)
NL (2) NL239535A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE632726A (en) * 1962-05-24 1900-01-01

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE676117C (en) * 1934-12-11 1939-05-26 I G Farbenindustrie Akt Ges Process for the production of high molecular weight polyamines
BE538464A (en) * 1954-05-26

Also Published As

Publication number Publication date
NL239535A (en)
NL125289C (en)
DE1131404B (en) 1962-06-14
FR1226159A (en) 1960-07-08
BE579238A (en)

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