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GB1390791A - Flame retarding textiles and paper - Google Patents

Flame retarding textiles and paper

Info

Publication number
GB1390791A
GB1390791A GB833072A GB833072A GB1390791A GB 1390791 A GB1390791 A GB 1390791A GB 833072 A GB833072 A GB 833072A GB 833072 A GB833072 A GB 833072A GB 1390791 A GB1390791 A GB 1390791A
Authority
GB
United Kingdom
Prior art keywords
alkyl
hydroxy
paper
textile
group
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
GB833072A
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.)
Stauffer Chemical Co
Original Assignee
Stauffer Chemical 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
Priority claimed from US05/118,164 external-priority patent/US3969437A/en
Application filed by Stauffer Chemical Co filed Critical Stauffer Chemical Co
Publication of GB1390791A publication Critical patent/GB1390791A/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
    • D06M15/43Amino-aldehyde resins modified by phosphorus compounds
    • D06M15/432Amino-aldehyde resins modified by phosphorus compounds by phosphonic acids or derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/28Phosphorus compounds with one or more P—C bonds
    • C07F9/38Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
    • C07F9/40Esters thereof
    • C07F9/4003Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
    • C07F9/4006Esters of acyclic acids which can have further substituents on alkyl
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6564Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
    • C07F9/6571Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms
    • C07F9/657163Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms the ring phosphorus atom being bound to at least one carbon atom
    • C07F9/657181Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms the ring phosphorus atom being bound to at least one carbon atom the ring phosphorus atom and, at least, one ring oxygen atom being part of a (thio)phosphonic acid derivative
    • 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
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/244Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus
    • D06M13/282Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus with compounds containing phosphorus
    • D06M13/288Phosphonic or phosphonous acids or derivatives thereof

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

1390791 Flame retarding textiles and paper STAUFFER CHEMICAL CO 23 Feb 1972 [23 Feb 1971 (2)] 8330/72 Heading DIP A process for flame retarding textiles and paper comprises (a) applying to the textile or paper a composition containing a pentavalent phosphorus ester having at least one C-bonded methylol group, dimethylol dihydroxy ethylene urea and an acid curing catalyst; and (b) curing the pentavalent phosphorus ester and the dimethylol dihydroxy ethylene urea on the textile or paper so as to effect coreaction of the ester and the dimethylol dihydroxy ethylene urea with one another in situ on the textile or paper to render the textile flame-retardant. The composition preferably contains the ester and the dimethylol dihydroxy ethylene urea in a weight ratio of between 3:1 and 1:2. The composition may further contain a peroxygen bleaching agent such as sodium perborate, a supplementary quantity of an aminoplast, a softening agent and a wetting agent. It may be applied from a solution in water, a halogenated hydrocarbon, or an emulsified mixture of a halogenated hydrocarbon and enough water to swell the fibres. The application may be at a pH between 3 and 6.7 and at a temperature between ambient and the curing temperature. The treated textile is heat cured at between 100 and 180‹C. The preferred phosphorus ester is O, O-diethyl N, N-bis (2-hydroxyethyl) aminomethyl phosphonate. Alternatively the phosphorus ester may have the structure I wherein R is a hydrocarbyl radical unsubstituted or substituted by hydroxy and/or a halogen; and R 1 and R 2 are organic radical selected from the group consisting of alkyl and alkoxy which can be unsubstituted or substituted by alkoxy, halogen or hydroxy; hydroxy polyalkyleneoxy; phenyl; halophenyl; amino-substituted alkyl; -O-alkylene-O- or O- alkyleneoxy alkylene-O bonded to the same or another pentavalent phosphorus ester group; amino; alkyl-substituted amino, or hydroxy alkyl-substituted amino, with the proviso that in the aforementioned groups there is at least one carbon-bonded methylol group. A second class of phosphorus esters has the general formula II wherein R 3 and R 4 are selected from the group consisting of lower alkyl, halogenated lower alkyl, lower alkoxy alkyl, lower hydroxy alkyl, lower alkoxy, lower hydroxyalkoxy, hydroxy polyalkyleneoxy and halogenated lower alkoxy, where "lower" corresponds to up to 8C atoms; and n is an integer from 1 to 6. A third class of phosphorus esters has the formula III wherein R 5 and R 6 are alkyl, hydroxyalkyl, alkoxyalkyl or hydroxyalkoxyalkyl (1-6C), the termini of an alkylene forming 6-membered ring or a halogenated analogue thereof, the termini of an alkylene or alkyleneoxyalkylene bonded to a further phosphorus ester group, hydroxypolyoxyalkylene or a hydroxy-substituted analogue thereof; R 7 and R 8 are hydrogen or alkyl (1-6C); m is an integer of 0 to 2; and n is an integer from 0 to 1. A fourth class of phosphorus compounds has the general formula IV wherein R 9 and R 10 can be the same or different and are selected from the group consisting of hydrogen, lower alkyl, lower hydroxyalkyl, lower haloalkyl and hydroxy ("lower" meaning 1-8C) with . the proviso that no more than one of R 9 and R 10 can be hydroxy. The preferred catalysts include zinc chloride, zinc nitrate, magnesium chloride, hydrochloric acid, ortho-phosphoric acid, and 2-amino-2-methyl propanol hydrochloride. The perborate bleach may comprise 5% by weight of the treatment bath and is preferably applied at a pH between 5 and 6.6. The preferred supplementary aminoplasts are tris (methoxymethyl) melamine and tris (methylol) melamine, optionally applied together with acetamide. The preferred softeners are stearamides and polyethylene emulsions. The preferred wetting agents are alkylaryl sulphonates and polyoxyethylene derivatives of alkylphenols. The textile materials may be cotton, cotton/polyester blends, viscose rayon, jute and products made from wood pulp and may be in the form of staple, filament, yarn or woven or non-woven fabric, e.g. apparel, bedding, tent cloth, carpets, home furnishings, aircraft and automobile interior fabrics and industrial fabrics. Reference has been directed by the comptroller to Specification 1336063.
GB833072A 1971-02-23 1972-02-23 Flame retarding textiles and paper Expired GB1390791A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US11816671A 1971-02-23 1971-02-23
US05/118,164 US3969437A (en) 1971-02-23 1971-02-23 Cyclic phosphorus esters

Publications (1)

Publication Number Publication Date
GB1390791A true GB1390791A (en) 1975-04-16

Family

ID=26816032

Family Applications (1)

Application Number Title Priority Date Filing Date
GB833072A Expired GB1390791A (en) 1971-02-23 1972-02-23 Flame retarding textiles and paper

Country Status (1)

Country Link
GB (1) GB1390791A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2117021A (en) * 1982-03-16 1983-10-05 Sandoz Products Ltd Flameproofing compositions

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2117021A (en) * 1982-03-16 1983-10-05 Sandoz Products Ltd Flameproofing compositions

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee