ES261545A1 - Textile materials and process for manufacturing them - Google Patents

Textile materials and process for manufacturing them

Info

Publication number
ES261545A1
ES261545A1 ES0261545A ES261545A ES261545A1 ES 261545 A1 ES261545 A1 ES 261545A1 ES 0261545 A ES0261545 A ES 0261545A ES 261545 A ES261545 A ES 261545A ES 261545 A1 ES261545 A1 ES 261545A1
Authority
ES
Spain
Prior art keywords
urea
acids
acid
liquor
cellulose
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
ES0261545A
Other languages
Spanish (es)
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.)
Bradford Dyers Association Ltd
Original Assignee
Bradford Dyers Association Ltd
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 Bradford Dyers Association Ltd filed Critical Bradford Dyers Association Ltd
Publication of ES261545A1 publication Critical patent/ES261545A1/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
    • D21H25/00After-treatment of paper not provided for in groups D21H17/00 - D21H23/00
    • D21H25/02Chemical or biochemical treatment
    • 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
    • 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
    • D21H17/47Condensation polymers of aldehydes or ketones
    • D21H17/49Condensation polymers of aldehydes or ketones with compounds containing hydrogen bound to nitrogen
    • 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
    • D21H5/00Special paper or cardboard not otherwise provided for
    • D21H5/12Special paper or cardboard not otherwise provided for characterised by the use of special fibrous materials
    • D21H5/1272Special paper or cardboard not otherwise provided for characterised by the use of special fibrous materials of fibres which can be physically or chemically modified during or after web formation
    • D21H5/1281Special paper or cardboard not otherwise provided for characterised by the use of special fibrous materials of fibres which can be physically or chemically modified during or after web formation by chemical treatment
    • 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
    • D21H11/00Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only
    • D21H11/16Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only modified by a particular after-treatment
    • D21H11/18Highly hydrated, swollen or fibrillatable fibres

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)
  • Coloring (AREA)

Abstract

Material consisting wholly or in part of cellulose or of a cellulose derivative which contains free hydroxyl groups, e.g. cellulose diacetate, is treated with an aqueous liquor which contains a methylated nitrogen containing compound or compounds or ether thereof or nitrogen containing compound containing C substituted methylol groups and an acid so that the material is swollen and maintained in the swollen condition while reaction therewith takes place and the acid then removed, e.g. by neutralizing and rinsing in water, and the material dried. The cellulosic material may be in the form of pulp, fibres, yarns, woven or knitted fabrics or sheet material, e.g. non woven fabrics, paper and regenerated cellulose films, alone or mixed with other fibres, e.g. wool, regenerated protein, nylon, polyethyleneterephthalate, cellulose triacetate or acrylic fibres. Suitable methylolated nitrogen compounds and ethers thereof are polymethylol derivatives of urea, dicyandiamide, adipamide, ethylene urea, dihydroxy ethylene urea, alkyl and alkoxy derivatives of ethylene urea, acetylene diurea, propyleneurea, melamine, ammeline, formoguanamine, triazones, e.g. methyl, ethyl and hydroxyethyl-triazones, hydantoin and substituted hydantoins, uron and substituted urons, and the compounds obtained by the reaction of pyruvic aldehyde or a -hydroxyadipaldehyde with urea and formaldehyde. When using methylol derivatives of urea the pH of the aqueous liquor should be 5-6 and long treatment times and high temperatures utilized or strong acids may be used if aldehydes, e.g. formaldehyde, glyoxal, pyruvicaldehyde or a -hydroxyadipaldehyde, or alcohols, e.g. methanol, glycol or glycerol, are added. Suitable acids are mineral acids, e.g. sulphuric, nitric, hydrochloric and phosphoric acids, strong organic acids, e.g. trichloracetic acid, and weak organic acids, e.g. formic, acetic, tartaric, citric and oxalic acids. The material may be treated by steeping it in a bath of acidic liquor for the appropriate reaction time, by circulating the acidic liquor by mechanical means through a mass of pulp or fibres or by padding, batching the material and allowing it to stand for the required period of time when wrapped in impervious material, e.g. polyethylene sheeting, to prevent drying out. The material is preferably treated at room temperature with a reaction liquor containing 1-10N sulphuric acid for 2-3 hours. Prior to treatment the material may be glazed or pretreated with steam or superheated steam, a swelling agent e.g. caustic soda, or a resin, e.g. polyvinyl alcohol. A particularly suitable composition for use in the treatment comprises 5-25 parts by weight of dimethylol dihydroxyethylene urea and 95-75 parts by weight of aqueous sulphuric acid of normality between 4N and 12,5N.ALSO:Material consisting wholly or in part of cellulose or of a cellulose derivative which contains free hydroxyl groups, e.g. cellulose diacetate, is treated with an aqueous liquor which contains a methylolated nitrogen containing compound or compounds or ether thereof or nitrogen containing compound containing substituted methylol groups and an acid so that the material is swollen and maintained in the swollen condition while reaction therewith takes place and the acid then removed, e.g. by neutralising and rinsing in water, and the material dried in order to improve its wet crease recovery, dimensional stability and ability to receive dyeing and finishing operations. The cellulosic material may be in the form of pulp fibres, yarns, woven or knitted fabrics or sheet material, e.g. non-woven fabrics, paper and regenerated cellulose films, alone or mixed with other fibres, e.g. wool, regenerated protein, nylon, polyethyleneterephthalate, cellulose triacetate or acrylic fibres. Suitable methylolated nitrogen compounds and ethers thereof are polymethylol derivatives of urea, dicyandiamide, adipamide, ethylene urea, dihydroxy ethylene urea, alkyl and alkoxy derivatives of ethylene urea, acetylene diurea, propyleneurea, melamine, ammeline, formoguanamine, triazones, e.g. methyl, ethyl and hydroxyethyl-triazones, hydantoin and substituted hydantoins, uron and substituted urons, and the compounds obtained by the reaction of pyruvic aldehyde or a -hydroxyadipaldehyde with urea and formaldehyde. When using methylol derivatives of urea the pH of the aqueous liquor should be 5-6 and long treatment times and high temperatures utilized or strong acids may be used if aldehydes, e.g. formaldehyde, glyoxal, pyruvicaldehyde or a -hydroxyadipaldehyde, or alcohols, e.g. methanol, glycol or glycerol, are added. Suitable acids are mineral acids, e.g. sulphuric, nitric, hydrochloric and phosphoric acids, strong organic acids, e.g. trichloracetic acid, and weak organic acids, e.g. formic, acetic, tartaric, citric and oxalic acids. The material may be treated by steeping it in a bath of acidic liquor for the appropriate reaction time, by circulating the acidic liquor by mechanical means through a mass of pulp or fibres or by padding, batching the material and allowing it to stand for the required period of time while wrapped in impervious material, e.g. polyethylene sheeting, to prevent drying out. The material is preferably treated at room temperature with a reaction liquor containing 1-1ON sulphuric acid for 2-3 hours. 2ON sulphuric acid may be used to obtain a parchmentising effect. Acid dispersible cellulose ethers may be included in the acid liquor. Fabrics may be pleated while in the wet state after impregnation, the treatment serving to set the pleats. Prior to treatment the material may be glazed or pretreated with steam or superheated steam, a swelling agent, e.g. caustic soda, or a resin, e.g. polyvinyl alcohol. The material may subsequently be treated with stiffening agents, softening agents, water repellents, e.g. waxes, silicones or fatty chain pyridinium compounds, fluorescent brighteners, resins, e.g. amino-formaldehyde condensates, or swelling agents, e.g. caustic soda, and dyed with direct cotton dyes, vat dyes, solubilised vat dyes, azoic dye combinations or reactive dyes.
ES0261545A 1959-10-08 1960-10-06 Textile materials and process for manufacturing them Expired ES261545A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB34193/59A GB905044A (en) 1959-10-08 1959-10-08 Chemical modification of cellulose and cellulose derivatives
GB1890960 1960-05-27

Publications (1)

Publication Number Publication Date
ES261545A1 true ES261545A1 (en) 1961-01-16

Family

ID=26253682

Family Applications (1)

Application Number Title Priority Date Filing Date
ES0261545A Expired ES261545A1 (en) 1959-10-08 1960-10-06 Textile materials and process for manufacturing them

Country Status (9)

Country Link
US (2) US3216780A (en)
BE (1) BE595844A (en)
CH (1) CH374624A (en)
DE (1) DE1419369A1 (en)
DK (1) DK108719C (en)
ES (1) ES261545A1 (en)
FR (1) FR1270888A (en)
GB (2) GB905044A (en)
NL (1) NL256665A (en)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3639096A (en) * 1964-10-19 1972-02-01 Dan River Inc Process of treating direct dyed cellulosic textiles with a mixture of aminoplast creaseproofing agents and products resulting therefrom
US3484182A (en) * 1966-07-01 1969-12-16 Monsanto Co Finish performance of fabrics comprised of synthetic fibers and cellulosic fibers
US3890095A (en) * 1967-04-05 1975-06-17 American Cyanamid Co Cellulosic textile finish with 1,3-dimethylol-4,5-dihydroxy-2-imidazolidinone, zinc nitrate and a sequestering agent
US3535141A (en) * 1967-04-17 1970-10-20 Deering Milliken Res Corp Process for making sail release synthetic textile
GB1273212A (en) * 1969-05-17 1972-05-03 English Calico Method of treating cellulosic material
US3664381A (en) * 1970-05-22 1972-05-23 Du Pont Press free textile fabric
US3936547A (en) * 1973-02-24 1976-02-03 Cassella Farbwerke Mainkur Aktiengesellschaft Process of preparing melamine resin films by impregnation of paper, cellulose, fleece or fabric
US4120647A (en) * 1976-06-04 1978-10-17 Ciba-Geigy Corporation Process for the dyeing of wool-containing fibre materials
EP0058138A3 (en) * 1981-02-11 1984-09-12 Ciba-Geigy Ag Process for setting wool yarn
GB2177732B (en) * 1985-07-11 1989-08-02 Bip Chemicals Ltd Process for treating textile fabrics and composition for use therein
GB8517740D0 (en) * 1985-07-13 1985-08-21 Wool Dev Int Textile treatment
FI80741C (en) * 1987-10-29 1990-07-10 Laennen Tehtaat Oy PAPER MODIFICATION.
CN111826962B (en) * 2020-08-03 2022-08-02 江苏阳光股份有限公司 Antibacterial finishing method for mercerized wool fabric

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE767329C (en) * 1933-11-25 1952-05-26 Raduner & Co Ag Process for finishing textile fabrics made from cellulose fibers
DE703207C (en) * 1934-10-16 1941-03-04 Boehme Fettchemie Ges M B H Method of making fabrics crease-resistant
US2022233A (en) * 1935-01-17 1935-11-26 Unyte Corp Co-amide resin and process of making same
US2137465A (en) * 1937-05-11 1938-11-22 Rohm & Haas Process of finishing textiles
US2709141A (en) * 1952-06-28 1955-05-24 Kendall & Co Resin-treated regenerated cellulose textile material and method of making the same
US2880114A (en) * 1955-05-04 1959-03-31 Samcoe Holding Corp Method of resin treating tubular knitted fabric
US3046079A (en) * 1960-05-24 1962-07-24 Wilson A Reeves Process of reacting partially swollen cotton textiles with aqueous solutions of specific aldehydes containing acid catalysts to produce wet and dry crease resistance

Also Published As

Publication number Publication date
GB905044A (en) 1962-09-05
CH1131560A4 (en) 1963-09-13
US3216780A (en) 1965-11-09
DE1419369A1 (en) 1968-12-12
NL256665A (en)
DK108719C (en) 1968-02-05
CH374624A (en) 1964-03-13
FR1270888A (en) 1961-09-01
GB971207A (en) 1964-09-30
US3216779A (en) 1965-11-09
BE595844A (en)

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