GB931559A - Creaseproofing of cellulosic materials - Google Patents

Creaseproofing of cellulosic materials

Info

Publication number
GB931559A
GB931559A GB3338159A GB3338159A GB931559A GB 931559 A GB931559 A GB 931559A GB 3338159 A GB3338159 A GB 3338159A GB 3338159 A GB3338159 A GB 3338159A GB 931559 A GB931559 A GB 931559A
Authority
GB
United Kingdom
Prior art keywords
dimethylol
crease
hydrogen
hexahydropyrimidone
creaseproofing
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
GB3338159A
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.)
Sun Chemical Corp
Original Assignee
Sun Chemical Corp
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 Sun Chemical Corp filed Critical Sun Chemical Corp
Publication of GB931559A publication Critical patent/GB931559A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/06—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D239/08—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms directly attached in position 2
    • C07D239/10—Oxygen or sulfur atoms
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
    • D06M15/423—Amino-aldehyde resins

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

Cellulosic fabric is crease-proofed by impregnating the material with an aqueous solution comprising a latent acidic catalyst and a creaseproofing compound having the general formula <FORM:0931559/IV(a)/1> wherein X is oxygen or sulphur and either (i) R is hydrogen and R1 is hydrogen as (ii) R is hydrogen or a C1-4 alkyl group and R1 is hydroxyl, and then drying the material and heating to cure the crease-proofing compound. The crease-proofing compounds may be admixed with a textile lubricant, latent acidic catalyst and a dispersing agent to form a concentrate which is diluted with water before use. In examples, cotton fabric is treated with an aqueous solution of (1) 1,3-dimethylol-hexahydropyrimidone-2 and zinc nitrate; (2) 1,3-dimethylol hexahydropyrimidthione-2 and mono-ammonium phosphate or (3) 1,3-dimethylol hexahydropyrimidone-2, emulsifiable polyethylene wax, polyethoxy nonyl phenol and 2-amino-2-methyl-1-propanol hydrochloride. Curing is preferably effected at 150 DEG -250 DEG C. Specification 931,560 is referred to.
GB3338159A 1958-10-31 1959-10-01 Creaseproofing of cellulosic materials Expired GB931559A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US77091058A 1958-10-31 1958-10-31

Publications (1)

Publication Number Publication Date
GB931559A true GB931559A (en) 1963-07-17

Family

ID=25090089

Family Applications (2)

Application Number Title Priority Date Filing Date
GB902063A Expired GB931560A (en) 1958-10-31 1959-10-01 Pyrimidones and pyrimidthiones
GB3338159A Expired GB931559A (en) 1958-10-31 1959-10-01 Creaseproofing of cellulosic materials

Family Applications Before (1)

Application Number Title Priority Date Filing Date
GB902063A Expired GB931560A (en) 1958-10-31 1959-10-01 Pyrimidones and pyrimidthiones

Country Status (1)

Country Link
GB (2) GB931560A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL137114B (en) * 1965-08-17

Also Published As

Publication number Publication date
GB931560A (en) 1963-07-17

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