GB1014884A - Epoxy resins and utilization thereof - Google Patents

Epoxy resins and utilization thereof

Info

Publication number
GB1014884A
GB1014884A GB2910362A GB2910362A GB1014884A GB 1014884 A GB1014884 A GB 1014884A GB 2910362 A GB2910362 A GB 2910362A GB 2910362 A GB2910362 A GB 2910362A GB 1014884 A GB1014884 A GB 1014884A
Authority
GB
United Kingdom
Prior art keywords
reacted
epon
product
treated
fibres
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
GB2910362A
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.)
Hawley Products Co
Original Assignee
Hawley Products 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 Hawley Products Co filed Critical Hawley Products Co
Publication of GB1014884A publication Critical patent/GB1014884A/en
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20Macromolecular organic compounds
    • D21H17/33Synthetic macromolecular compounds
    • D21H17/46Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H17/54Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B15/00Preparation of other cellulose derivatives or modified cellulose, e.g. complexes
    • C08B15/05Derivatives containing elements other than carbon, hydrogen, oxygen, halogens or sulfur
    • C08B15/06Derivatives containing elements other than carbon, hydrogen, oxygen, halogens or sulfur containing nitrogen, e.g. carbamates
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B31/00Preparation of derivatives of starch
    • 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
    • C08G59/02Polycondensates containing more than one epoxy group per molecule
    • C08G59/10Polycondensates containing more than one epoxy group per molecule of polyamines with epihalohydrins or precursors thereof
    • 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
    • C08G59/182Macromolecules 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 using pre-adducts of epoxy compounds with curing agents
    • C08G59/184Macromolecules 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 using pre-adducts of epoxy compounds with curing agents with amines
    • 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
    • C08G59/50Amines
    • C08G59/5006Amines aliphatic
    • 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
    • D06M15/55Epoxy 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)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • Materials Engineering (AREA)
  • Textile Engineering (AREA)
  • Paper (AREA)
  • Epoxy Resins (AREA)

Abstract

Hydrophilic, thermoplastic resins which are soluble in a 2.5% by wt. hydrochlorine acid solution are prepared by reacting an epoxide with a polyamine containing more than two carbon atoms and at least two amino groups, each having at least one hydrogen atom attached to nitrogen, but not more than two primary amino groups; and reacting the product with an epoxide or with a compound which introduces an epoxy group into the molecule under conditions to avoid gel formation. Suitable epoxide starting materials are the diglycidyl ether of 4,41-dihydroxydiphenyldimethylenethane; butadiene diepoxide; compounds of formula <FORM:1014884/C3/1> or of formula <FORM:1014884/C3/2> or allyl glycidyl ether. Suitable amines are 1,3-propylene diamine N-methyl-1,2-propylene diamine, N-propyl propylene diamine, butylene-1,2-diamine, hexamethylene diamine, diethylene triamine, triethylene tetramine, tetraethylenepentamine, di-1,2-propylenetriamine. In examples resins are prepared from I. The reaction product of EPON 828 with diethylene triamine was reacted with further EPON 828. The second reaction was stopped at incipient gelation by acidification. II (a) Hexamethylene diamine was reacted with two lots of EPON 828. (b) Triethylene tetramine was similarly reacted. III Tetraethylene pentamine was reacted with two lots of (a) butadiene dioxide; (b) EPON 812; and (c) resorcinol diglycidyl ether. IV Tetraethylene pentamine was reacted with EPON 828 and the product with epichlorohydrin. V Tetraethylene pentamine was reacted with two lots of EPON 828. If desired the epoxidized products of the invention may be reacted with formaldehyde to increase their reactivity (see Examples VI-IX). Ethylenically unsaturated groups may be introduced into the epoxides of the invention to permit copolymerization with for example, acrylonitrile, styrene, vinyl toluene, acrylic acid, and methyl or ethyl methacrylates. In Example X, allyl glycidyl ether is reacted with tetraethylene pentamine and the product reacted with EPON 828, and in Example XI, the product of Example X was reacted with formaldehyde. The epoxy-containing products of the invention may also be reacted with long chain fatty amines, e.g. dodecylamine, tetradecylamine hexadecylamine oleylamine, or N - alkyl-trimethylene diamines prepared by reacting long chain fatty amines with acrylonitrile and then hydrogenating. In Example XII an N-alkyl trimethylene diamine known as Duomeen O, and tetraethylene pentamine were reacted with EPON 828 in two stages. In Example XIII the product of Example XII was reacted with formaldehyde. Example XIV reacts tetraethylene pentamine and dodecylamine with two lots of EPON 828, and the product was reacted in Example XV with formaldehyde. The products of the invention on cationic water-soluble resins useful for treating anionic fibres, e.g. cellulose in the manufacture of paper, wall board and other fibrous articles. They are usually aqueous solutions but may be dissolved in organic solvents. Some of the products are useful sizing agents for glass fibre in polyester mouldings. They may also be used to modify starch products. In Example XXIII potato starch was stirred into water and a resin prepared from diethylene triamine reacted in two stages with EPON 828 to yield a cationic starch which can be transformed into a white opaque gel by addition of a water-soluble phenolic resin.ALSO:Anionic fibres, e.g. cellulose are treated with thermoplastic cationic resins which are soluble in dil HCl and are prepared by reacting an epoxide with a polyamine, and introducing epoxy groups into the product by reaction to the point of incipient gelation with an epoxide. The fibres are used for making paper, mouldings, wallboard or other fibrous articles. If desired the resins may be rendered non active by reaction with formaldehyde. In Example XVI paper was prepared from cellulose fibre treated with a resin derived from di-ethylene triamine by a treatment in two stages with an epoxide known as EPON 828. In Example XVII sisal fibres treated with the same resin are used, either alone or mixed with unmodified sisal fibres. The treated fibres are oil-wetting. In Example XVII, the resin is applied to paper as a tub size. Cellulon treated according to the invention has the ability to bond or adhere to materials such as polystyrene, petroleum resins, oleoresinous varnishes, and polyester resins. In Example XIX cellulose was treated with a resin from tetraethylene pentamine treated with two successive lots of EPON 828, both alone and with formaldehyde, and a phenolic resin known as Resinon 594 was used as a beater addition to the modified cellulose a production of paper. Examples XX to XXII describe similar treatments of cellulon fibres.
GB2910362A 1961-08-07 1962-07-30 Epoxy resins and utilization thereof Expired GB1014884A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US12951661A 1961-08-07 1961-08-07

Publications (1)

Publication Number Publication Date
GB1014884A true GB1014884A (en) 1965-12-31

Family

ID=22440366

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2910362A Expired GB1014884A (en) 1961-08-07 1962-07-30 Epoxy resins and utilization thereof

Country Status (3)

Country Link
BE (1) BE621064A (en)
DE (1) DE1520057A1 (en)
GB (1) GB1014884A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0758660A2 (en) * 1995-08-14 1997-02-19 Air Products And Chemicals, Inc. Advanced polyamine adduct epoxy resin curing agent for use in two component waterborne coating systems
WO1997023564A1 (en) * 1995-12-21 1997-07-03 The Dow Chemical Company Compositions comprising hydroxy-functional polymers
WO2012025710A2 (en) 2010-08-25 2012-03-01 The Lightning Car Company Limited Electric motor vehicle
CN103601871A (en) * 2013-11-19 2014-02-26 湖南神力实业有限公司 Novel epoxy curing agent and synthesis method thereof

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109847715A (en) * 2018-12-05 2019-06-07 广东工业大学 A kind of preparation method of amide group modified polystyrene system super high cross-linked adsorbing resin

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0758660A2 (en) * 1995-08-14 1997-02-19 Air Products And Chemicals, Inc. Advanced polyamine adduct epoxy resin curing agent for use in two component waterborne coating systems
EP0758660A3 (en) * 1995-08-14 1997-05-28 Air Prod & Chem Advanced polyamine adduct epoxy resin curing agent for use in two component waterborne coating systems
WO1997023564A1 (en) * 1995-12-21 1997-07-03 The Dow Chemical Company Compositions comprising hydroxy-functional polymers
EP1041116A2 (en) * 1995-12-21 2000-10-04 The Dow Chemical Company Compositions comprising hydroxy-functional polymers
EP1041116A3 (en) * 1995-12-21 2002-06-05 The Dow Chemical Company Compositions comprising hydroxy-functional polymers
WO2012025710A2 (en) 2010-08-25 2012-03-01 The Lightning Car Company Limited Electric motor vehicle
CN103601871A (en) * 2013-11-19 2014-02-26 湖南神力实业有限公司 Novel epoxy curing agent and synthesis method thereof

Also Published As

Publication number Publication date
BE621064A (en)
DE1520057A1 (en) 1970-03-26

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