GB766273A - Improvements in or relating to the curing of polyepoxides - Google Patents

Improvements in or relating to the curing of polyepoxides

Info

Publication number
GB766273A
GB766273A GB20967/54A GB2096754A GB766273A GB 766273 A GB766273 A GB 766273A GB 20967/54 A GB20967/54 A GB 20967/54A GB 2096754 A GB2096754 A GB 2096754A GB 766273 A GB766273 A GB 766273A
Authority
GB
United Kingdom
Prior art keywords
polyether
fluoborate
agents
glycidyl
curing
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
GB20967/54A
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.)
Bataafsche Petroleum Maatschappij NV
Original Assignee
Bataafsche Petroleum Maatschappij NV
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 Bataafsche Petroleum Maatschappij NV filed Critical Bataafsche Petroleum Maatschappij NV
Publication of GB766273A publication Critical patent/GB766273A/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
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/40Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
    • C08G59/4007Curing agents not provided for by the groups C08G59/42 - C08G59/66
    • 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

Landscapes

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

Abstract

A glycidyl polyether from epichlorhydrin and a polyhydric phenol or alcohol is cured by a salt of a metal of atomic weight between 24 and 210 with an inorganic acid of the formula Ha[XwFy], wherein X is a non-metal of atomic weight above 2, w and y are integers and a is the valency of the acid. Preferred salts are fluoborates or fluosilicates of metals of Groups 1 to IV and VIII, e.g. copper, zinc, iron, cadmium, nickel, cobaltous, magnesium and strontium fluoborate and cobaltous, copper and magnesium fluosilicate. The process is particularly applicable for hardening glycidyl ethers which have been used for treating textiles (see Group IV (c)). The polyethers and curing agents may be mixed in solvents to which diluents may be added or the polyethers may be used in emulsion form. Lists of suitable solvents and diluents and emulsifying agents are given. Pigments, plasticisers and other resins may also be added. Textile softening-agents, e.g. epoxidized oils, glycidyl-D -decyl ether, pentadecyl phenol, octadecyl succinic acid, sulphonated waxes or alcohols, dimerized long-chain acids, or polyglycol fatty acid esters may be added to textile treating compositions. In Example I zinc fluoborate was used as curing agent for a glycidyl polyether from glycerol in an aqueous textile treating composition containing also methyl cellulose, a copolymer of vinyl methyl ether and maleic anhydride, and a polyglycol fatty acid ester. II. Fluoborates of a number of different metals are compared as curing agents in textile treating compositions. III. Zinc fluoborate is used as curing agent in a number of textile treating compositions containing different softening agents. IV. Films are prepared from a mixture of lead fluoborate with a glycidyl polyether prepared from epichlorhydrin and 2 - hydroxy - ethoxy methyl - 2,4 - dimethyl pentanediol-1,5. V. Films are prepared from a mixture of cadmium fluoborate with a polyether from bisphenol and epichlorohydrin. VI is similar to V but uses copper fluoborate.ALSO:Textile materials are impregnated with compositions containing a glycidyl polyether of a polyhydric phenol or alcohol and a metal fluoborate or fluosilicate and the polyether is cured. The treated materials have improved resistance to shrinkage, good wrinkle recovery, resistance to scorch and laundering properties and no chlorine retention. The polyether may be applied first and a solution of the curing salt sprayed on to the material. The compositions may be aqueous solutions or emulsions or organic solvents may be used. Solvents and emulsifying agents are listed in the Specification. Curing is effected by heating. Plasticizers or softening agents, e.g. epoxidized glyceride, epoxidized soya bean oil, glycidyl delta decyl ether, pentadecyl phenol, octadecyl or octadecenyl succinic acid, sulphonated waxes or alcohols, dimerized long chain fatty acids or nonionic fatty acid esters of higher polyglycols may be included in the compositions. The solutions may be applied to one surface only e.g. of a fabric with a silk face and cotton back. They may also be applied locally to fabrics. Repeated applications may be made, the amount of polyether added to the fabric depending on the purpose for which the fabric is required. The fabric may be for example of cotton, linen, natural or artificial silk, jute, rayon, or wool and may be woven, knitted or netted. Threads, fibres or filaments may also be treated. In examples I cotton cloth was impregnated with an aqueous solution containing a polyether from glycerol and epichlorohydrin, methyl cellulose, a copolymer of vinyl methyl ether and maleic anhydride, a polyglycol fatty acid ester and zinc fluoborate as curing agent, dried and cured at 160 DEG C. for 5 mins. The properties of the treated cloth are compared with those of cloth treated with other materials. II Fluoborates of a number of different metals were employed as curing agents in textile-treating compositions of the kind described in Example I and the wrinkle recovery values of the treated cotton sheets were compared. III A series of impregnating solutions as described in Example I but with different softening agents were used on cotton cloth and the properties of the treated cloth were compared.
GB20967/54A 1953-07-21 1954-07-19 Improvements in or relating to the curing of polyepoxides Expired GB766273A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US344561XA 1953-07-21 1953-07-21

Publications (1)

Publication Number Publication Date
GB766273A true GB766273A (en) 1957-01-16

Family

ID=21876535

Family Applications (1)

Application Number Title Priority Date Filing Date
GB20967/54A Expired GB766273A (en) 1953-07-21 1954-07-19 Improvements in or relating to the curing of polyepoxides

Country Status (6)

Country Link
BE (1) BE530494A (en)
CH (1) CH344561A (en)
DE (1) DE1105376B (en)
FR (1) FR1109462A (en)
GB (1) GB766273A (en)
NL (2) NL95049C (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3242130A (en) * 1961-11-09 1966-03-22 Lubrizol Corp Phosphorodithioic zinc salt based corrosion inhibiting composition comprising an epoxy resin, acylated polyamine and filler
US3432440A (en) * 1965-02-11 1969-03-11 Celanese Coatings Co Epoxy curing agents comprising a fluoborate salt and a hydrolyzable ester
US4092296A (en) * 1973-08-13 1978-05-30 Skiff Russell A Epoxy resin compositions
US10617617B1 (en) 2018-12-04 2020-04-14 Momentive Performance Materials Inc. Polycarboxylic acid compounds for the treatment of fibrious amino acid based substrates, especially hair
US11090255B2 (en) 2018-12-04 2021-08-17 Momentive Performance Materials Inc. Use of polycarboxylic acid compounds for the treatment of fibrious amino acid based substrates, especially hair
US11179312B2 (en) 2017-06-05 2021-11-23 Momentive Performance Materials Inc. Aqueous compositions for the treatment of hair

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1200349A (en) * 1981-12-14 1986-02-04 Thomas F. Brownscombe Curable epoxy compositions, their preparation and formed articles therefrom
US4751143A (en) * 1984-09-20 1988-06-14 Celanese Corporation Process for treating chemically stabilized, adhesive activated polyester material, polyester material treated by the process and an improved finish composition

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL67492C (en) * 1945-07-13 1900-01-01
AT172353B (en) * 1948-10-01 1952-09-10 Hoechst Ag Process for the production of compounds with high chemical resistance that harden quickly in the cold

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3242130A (en) * 1961-11-09 1966-03-22 Lubrizol Corp Phosphorodithioic zinc salt based corrosion inhibiting composition comprising an epoxy resin, acylated polyamine and filler
US3432440A (en) * 1965-02-11 1969-03-11 Celanese Coatings Co Epoxy curing agents comprising a fluoborate salt and a hydrolyzable ester
US4092296A (en) * 1973-08-13 1978-05-30 Skiff Russell A Epoxy resin compositions
US11179312B2 (en) 2017-06-05 2021-11-23 Momentive Performance Materials Inc. Aqueous compositions for the treatment of hair
US10617617B1 (en) 2018-12-04 2020-04-14 Momentive Performance Materials Inc. Polycarboxylic acid compounds for the treatment of fibrious amino acid based substrates, especially hair
WO2020117509A1 (en) 2018-12-04 2020-06-11 Momentive Performance Materials Inc. Polycarboxylic acid compounds for the treatment of fibrous amino acid based substrates, especially hair
US11090255B2 (en) 2018-12-04 2021-08-17 Momentive Performance Materials Inc. Use of polycarboxylic acid compounds for the treatment of fibrious amino acid based substrates, especially hair

Also Published As

Publication number Publication date
NL189324B (en)
FR1109462A (en) 1956-01-30
NL95049C (en)
DE1105376B (en) 1961-04-27
CH344561A (en) 1960-02-15
BE530494A (en)

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