GB872656A - Improvements in the production of aminoplastic precondensates - Google Patents

Improvements in the production of aminoplastic precondensates

Info

Publication number
GB872656A
GB872656A GB17666/58A GB1766658A GB872656A GB 872656 A GB872656 A GB 872656A GB 17666/58 A GB17666/58 A GB 17666/58A GB 1766658 A GB1766658 A GB 1766658A GB 872656 A GB872656 A GB 872656A
Authority
GB
United Kingdom
Prior art keywords
formaldehyde
reaction
amino
epihalohydrin
catalyst
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
GB17666/58A
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.)
Courtaulds Inc
Original Assignee
Courtaulds Inc
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 Courtaulds Inc filed Critical Courtaulds Inc
Publication of GB872656A publication Critical patent/GB872656A/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
    • D06M15/39Aldehyde resins; Ketone resins; Polyacetals
    • D06M15/423Amino-aldehyde resins
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07GCOMPOUNDS OF UNKNOWN CONSTITUTION
    • C07G99/00Subject matter not provided for in other groups of this subclass
    • 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
    • C08G12/00Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C08G12/02Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
    • 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
    • C08G12/00Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C08G12/02Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
    • C08G12/40Chemically modified polycondensates

Abstract

In the process of the parent Specification in which formaldehyde is reacted with the adduct of an epihalogenhydrin and a resin forming amino compound, two improvements are described: (1) the reaction is effected in the presence of a hydroxide of Ca, Ba, Mg or Sr, and (2) the methylol groups of the reaction product are alkylated with an aliphatic hydrocarbon radical of C1-6. Urea and/or melamine are the only amino-compounds disclosed, and epichlorohydrin is the only epihalohydrin. In process (2) the formaldehyde reaction may have been carried out in the presence of NaOH, and if phosphoric acid is used as the subsequent alkylating catalyst, the resultant sodium phosphate may be filtered off; HCl is also mentioned as an alkylating catalyst. Aqueous solutions of the products of either improved process are used to impregnate cellulosic textile material (see Group IV(c)), in which case MgCl2 may be added as a hardener. In the examples the amino compound and the epihalohydrin are reacted in aqueous solution and the formaldehyde is in aqueous or methanolic solution.ALSO:In the process of the parent Specification in which formaldehyde is reacted with the adduct of an epihalogenhydrin and a resin forming amino compound, two improvements are described:-(i) the reaction is effected in the presence of a hydroxide of Ca, Ba, Mg or Sr, and (ii) the methylol groups of the reaction product are alkylated with an aliphatic hydrocarbon radical of C1-C6. Urea and/or melamine are the only amino compounds disclosed, and epichlorohydrin is the only epihalohydrin. In process (ii) the formaldehyde reaction may have been carried out in the presence of NaOH, and if phosphoric acid is used as the subsequent alkylating catalyst, the resultant sodium phosphate may be filtered off; HCl is also mentioned as an alkylating catalyst. Aqueous solutions of the products of either improved process (see Group IV(a)) may be used to impregnate cellulosic textile materials (see Group IV(c)). In the examples the amino compound and the epihalohydrin are reacted in aqueous solution and the formaldehyde is in aqueous or methanolic solution.ALSO:Cellulosic textile materials, e.g. cellulose, regenerated cellulose, modified cellulose and viscose rayon staple which has never been dried, may be impregnated with an aqueous solution of a stable, water-soluble, aminoplast precondensate described below, and heated to insolubilize the resin and reduce the water imbibition of the impregnated material. The precondensates are modified forms of the reaction products of formaldehyde with the adduct of an epihalogenhydrin and a resin-forming amino-compound of the parent Specification. The modifications are either in the catalyst (see Groups IV(a) and IV(b)) or in that the methylol groups of the reaction product are alkylated with an aliphatic C1-6 hydrocarbon radical. Urea and/or melamine are the only amino compounds disclosed, and epichlorohydrin is the only epithalohydrin. Magnesium chloride may be added as a catalyst. Examples are given.
GB17666/58A 1955-02-22 1958-06-03 Improvements in the production of aminoplastic precondensates Expired GB872656A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB5235/55A GB796815A (en) 1955-02-22 1955-02-22 Improvements in and relating to the production of an aminoplast precondensate for the treatment of cellulosic textile materials
US872656XA 1957-06-04 1957-06-04

Publications (1)

Publication Number Publication Date
GB872656A true GB872656A (en) 1961-07-12

Family

ID=62529122

Family Applications (2)

Application Number Title Priority Date Filing Date
GB5235/55A Expired GB796815A (en) 1955-02-22 1955-02-22 Improvements in and relating to the production of an aminoplast precondensate for the treatment of cellulosic textile materials
GB17666/58A Expired GB872656A (en) 1955-02-22 1958-06-03 Improvements in the production of aminoplastic precondensates

Family Applications Before (1)

Application Number Title Priority Date Filing Date
GB5235/55A Expired GB796815A (en) 1955-02-22 1955-02-22 Improvements in and relating to the production of an aminoplast precondensate for the treatment of cellulosic textile materials

Country Status (3)

Country Link
DE (1) DE1094225B (en)
FR (1) FR1148813A (en)
GB (2) GB796815A (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL247847A (en) * 1959-01-29
BE592464A (en) * 1959-07-11
US4396390A (en) * 1981-09-04 1983-08-02 Springs Mills, Inc. Aqueous formaldehyde textile finishing process
WO2019213092A1 (en) * 2018-05-01 2019-11-07 Georgia-Pacific Chemicals Llc Binder compositions and processes for making and using same
CN114560650A (en) * 2022-02-25 2022-05-31 娄底潇湘职业学院 High-strength building material and preparation method thereof

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL174182B (en) * 1951-12-01 British Petroleum Co BURNER.
US2730427A (en) * 1952-08-13 1956-01-10 American Cyanamid Co Shrinkage control of cellulosic and wool textiles with diglycidyl ether compounds

Also Published As

Publication number Publication date
DE1094225B (en) 1960-12-08
GB796815A (en) 1958-06-18
FR1148813A (en) 1957-12-16

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