EP0359039A2 - Procédé d'apprêt infraissable de matériaux textiles - Google Patents

Procédé d'apprêt infraissable de matériaux textiles Download PDF

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Publication number
EP0359039A2
EP0359039A2 EP89116059A EP89116059A EP0359039A2 EP 0359039 A2 EP0359039 A2 EP 0359039A2 EP 89116059 A EP89116059 A EP 89116059A EP 89116059 A EP89116059 A EP 89116059A EP 0359039 A2 EP0359039 A2 EP 0359039A2
Authority
EP
European Patent Office
Prior art keywords
finishing
textile materials
alkyl
wash
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.)
Withdrawn
Application number
EP89116059A
Other languages
German (de)
English (en)
Other versions
EP0359039A3 (fr
Inventor
Matthias Dr. Kummer
Toni Simenc
Werner Dr. Streit
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.)
BASF SE
Original Assignee
BASF SE
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 BASF SE filed Critical BASF SE
Publication of EP0359039A2 publication Critical patent/EP0359039A2/fr
Publication of EP0359039A3 publication Critical patent/EP0359039A3/fr
Withdrawn legal-status Critical Current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
    • 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
    • D06M13/322Treating 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 nitrogen
    • D06M13/402Amides imides, sulfamic acids
    • D06M13/432Urea, thiourea or derivatives thereof, e.g. biurets; Urea-inclusion compounds; Dicyanamides; Carbodiimides; Guanidines, e.g. dicyandiamides
    • 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
    • D06M15/45Use of special catalysts

Definitions

  • the object of the invention is to provide a method for easy care of textile materials consisting of cellulose fibers or containing cellulose fibers in a mixture with other fibers using formaldehyde-free finishing agents, in which one achieves finishing effects while maintaining high degrees of whiteness finished textile goods can be compared with the effects of formaldehyde-containing finishing agents in relation to the shrink and crease resistance behavior.
  • Textile materials are understood to mean, for example, fabrics, knitted fabrics, knitted fabrics, yarns and fibers in all processing stages.
  • the textile materials either consist of cellulose fibers or contain cellulose fibers in a mixture with other fibers, e.g. in a mixture with polyester fibers, polyamide fibers such as nylon, wool and polyacrylonitrile fibers.
  • the textile materials are impregnated with an aqueous liquor which contains an finishing agent and a catalyst for crosslinking the finishing agent.
  • a procedure is also possible in which the textile materials are first impregnated with an aqueous liquor which only contains the finishing agent and the catalyst is then applied to the fabric in a separate process step.
  • the mode of operation is preferred in which the finishing agent and catalyst are applied to the textile material in solution in a liquor.
  • Compounds of this type can be obtained, for example, by the process known from EP-PS 00 36 076. Accordingly, they are obtained by condensing compounds such as N, N'-dimethylurea, N-methylurea, N, N'-diethylurea, N-ethylurea, Nn-propylurea, N-isopropylurea, N, N-di-n-propylurea, N, N'-di-isopropylurea with glyoxal in the acidic pH range.
  • the molar ratio of the substituted ureas to glyoxal is 1 to 1.1 to 1.
  • the compound of formula I is preferably used as the finishing agent in which the substituents R1 and R2 are a methyl group and the substituents R3 and R4 are each hydrogen, ie N, N '-Dimethyl-4,5-dihydroxyethylene urea.
  • the concentration of the compounds of the formula I in the finishing liquor is 20 to 100, preferably 30 to 60 g / l.
  • the equipment fleet contains as another essential component (b) zinc fluoroborate or mixtures of zinc fluoroborate with other catalysts customary in high refinement, such as magnesium chloride, magnesium hydrogen phosphate, magnesium fluoroborate, aluminum chloride, aluminum sulfate, zinc nitrate or zinc chloride.
  • the finishing liquor contains, based on the finishing agents of formula I dissolved therein, 4 to 14 and preferably 8 to 14% by weight of zinc fluoroborate or the mixtures of zinc fluoroborate in question with the other catalysts customarily used in high refinement.
  • the amount of zinc fluoroborate in all mixtures should be chosen so that at least 50% by weight of zinc fluoroborate, based on the finishing agent (a), is used.
  • the catalyst mixtures those of zinc and magnesium fluoroborate are of particular interest.
  • the other catalysts for high refinement which can optionally be used together with zinc fluoroborate are used in amounts of 0 to 8% by weight, based on the finishing agent (a).
  • the equipment fleet contains at least one compound of the formulas as a further component (c)
  • the compounds of formulas II and III can be used either alone or in a mixture. They are contained in the equipment fleet in amounts of 0.01 to 1.0, preferably 0.05 to 0.5% by weight, based on the fleet.
  • the finishing liquor may optionally also contain other customary auxiliaries, for example water repellents, plasticizers, leveling agents, wetting agents and finishing agents and handle variators.
  • Hydrophobing agents are, for example, aluminum or zirconium-containing paraffin wax emulsions and silicone-containing preparations. Oxygenation products of higher fatty acids, fatty alcohols or fatty acid amides, higher molecular weight polyglycol ethers, higher fatty acids, fatty alcohol sulfonates and N-stearylurea compounds may be mentioned as plasticizers.
  • Leveling agents can be used water-soluble salts of acidic esters of polybasic acids with ethylene oxide or propylene oxide adducts, longer-chain oxyalkylatable basic bases.
  • Wetting agents are, for example, alkylnaphthalenesulfonic acids, the alkali metal salts of sulfonated succinic acid dioctyl ester and the addition products of alkylene oxides with fatty alcohols, alkylphenols or fatty amines.
  • Cellulose ethers or esters and alginates are suitable as finishing agents.
  • Dispersions of synthetic polymers and polycondensates are also suitable for this purpose; the auxiliaries which may be considered are generally used in amounts of 0.3 to 4, preferably 1 to 2.5,% by weight, based on the dry textile material.
  • Suitable handle variators for the process according to the invention are very well silicone softeners, preferably amino-functional polydimethylsiloxanes with a content of 0.2 to 5.0 percent by weight of amine, based on the remaining polydimethylsiloxane. This not only gives the finished goods a very soft feel, but also their wrinkling behavior is positively influenced.
  • the textile materials are impregnated with finishing liquors of the type described above.
  • the only essential for the success of the method according to the invention is the fact that the constituents specified under (a), (b) and (c) are applied to the textile material.
  • the easiest way to meet this requirement is to dissolve the three components mentioned in an aqueous liquor and apply them to the textile material.
  • each component can also be dissolved in an aqueous liquor and applied to the textile material.
  • the easiest way to treat the textile material with the aqueous liquor is by means of a padder and pressing off the excess liquor.
  • the fleet recordings are in the range of 50 to 120%.
  • it is also possible to treat the textile materials with components (a) to (c) by spraying, splashing or foam application.
  • the impregnated textile materials are dried and then fixed, in which the textile material is briefly heated to temperatures in the range from 140 to 180.degree.
  • the finishing agents are cross-linked with the cellulose fibers and with each other.
  • the fixing takes about 20 seconds to 7 minutes, preferably 40 to 280 seconds. The higher the temperature when fixing, the shorter the dwell time at the temperature used in each case.
  • the following examples and comparative examples illustrate the degree of easy care equipment based on the following characteristics. Dry crease angle (sum of warp and weft according to DIN 53 890), Wet crease angle (Tootal method BP 727 890) Monsanto picture, md, after a single 20-minute wash at 60 ° C, Wash shrink for warp and weft after washing once every 20 minutes at 60 ° C, tear strength (weft) measured according to ASTM D 1682-84-175 and Whiteness measured in percent using an Elrepho photometer.
EP19890116059 1988-09-13 1989-08-31 Procédé d'apprêt infraissable de matériaux textiles Withdrawn EP0359039A3 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE3831093 1988-09-13
DE19883831093 DE3831093A1 (de) 1988-09-13 1988-09-13 Verfahren zur pflegeleichtausruestung von textilen materialien

Publications (2)

Publication Number Publication Date
EP0359039A2 true EP0359039A2 (fr) 1990-03-21
EP0359039A3 EP0359039A3 (fr) 1991-07-31

Family

ID=6362848

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19890116059 Withdrawn EP0359039A3 (fr) 1988-09-13 1989-08-31 Procédé d'apprêt infraissable de matériaux textiles

Country Status (4)

Country Link
EP (1) EP0359039A3 (fr)
JP (1) JPH02112478A (fr)
DE (1) DE3831093A1 (fr)
DK (1) DK448489A (fr)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0515900A2 (fr) * 1991-05-31 1992-12-02 BASF Aktiengesellschaft Catalyseur pour l'ennoblissement de textiles
EP0682145A2 (fr) * 1994-05-12 1995-11-15 Ciba-Geigy Ag Traitement textile
WO1996007780A1 (fr) * 1994-09-06 1996-03-14 Basf Aktiengesellschaft Procede de fabrication de fibres de cellulose
US5707404A (en) * 1994-01-14 1998-01-13 Westpoint Stevens, Inc. Formaldehyde free method for imparting permanent press properties to cotton and cotton blends
US6117189A (en) * 1994-05-12 2000-09-12 Ciba Specialty Chemicals Corporation Protective method
CN101429344B (zh) * 2008-12-08 2012-07-04 浙江传化华洋化工有限公司 六磺酸类液体荧光增白剂的制备方法

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109797545B (zh) * 2019-01-17 2021-07-16 广东溢达纺织有限公司 高白度的纺织物免烫整理方法以及纺织物

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2154986A1 (de) * 1971-11-05 1973-05-10 Pfersee Chem Fab Verfahren zur hochveredlung von geweben oder gewirken
JPS59116476A (ja) * 1982-12-21 1984-07-05 住友化学工業株式会社 繊維の樹脂加工方法

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2154986A1 (de) * 1971-11-05 1973-05-10 Pfersee Chem Fab Verfahren zur hochveredlung von geweben oder gewirken
JPS59116476A (ja) * 1982-12-21 1984-07-05 住友化学工業株式会社 繊維の樹脂加工方法

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
CHEMICAL ABSTRACTS, vol. 95, no. 8, 24 August 1981 Columbus, Ohio, USA "RESIN FINISHING OF TEXTILES" & JP-A-8105868 (07/02/1981)(SHIN NISSO KAKO CO) Seite 69; rechte Spalte; ref. no. 63641 *
WPIL, FILE SUPPLIER, DERWENT PUBLICATIONS LTD.; LONDON, GB; & JP-A-59-116 476 (SUMITOMO) 05-07-1984 *

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0515900A3 (en) * 1991-05-31 1993-04-14 Basf Aktiengesellschaft Catalyst for the finishing of textiles
US5246904A (en) * 1991-05-31 1993-09-21 Basf Aktiengesellschaft Catalyst for the wash-and-wear finishing of textiles
EP0515900A2 (fr) * 1991-05-31 1992-12-02 BASF Aktiengesellschaft Catalyseur pour l'ennoblissement de textiles
US5707404A (en) * 1994-01-14 1998-01-13 Westpoint Stevens, Inc. Formaldehyde free method for imparting permanent press properties to cotton and cotton blends
EP0682145A3 (fr) * 1994-05-12 1998-08-26 Ciba SC Holding AG Traitement textile
EP0682145A2 (fr) * 1994-05-12 1995-11-15 Ciba-Geigy Ag Traitement textile
US6117189A (en) * 1994-05-12 2000-09-12 Ciba Specialty Chemicals Corporation Protective method
US5776394A (en) * 1994-09-06 1998-07-07 Basf Aktiengesellschaft Process for manufacturing cellulose fibres
EP0984084A2 (fr) * 1994-09-06 2000-03-08 Basf Aktiengesellschaft Procédé de fabrication de fibres de cellulose
EP0985747A2 (fr) * 1994-09-06 2000-03-15 Basf Aktiengesellschaft Procédé de fabrication de fibres de cellulose
EP0985747A3 (fr) * 1994-09-06 2000-04-19 Basf Aktiengesellschaft Procédé de fabrication de fibres de cellulose
EP0984084A3 (fr) * 1994-09-06 2000-04-19 Basf Aktiengesellschaft Procédé de fabrication de fibres de cellulose
WO1996007780A1 (fr) * 1994-09-06 1996-03-14 Basf Aktiengesellschaft Procede de fabrication de fibres de cellulose
CN101429344B (zh) * 2008-12-08 2012-07-04 浙江传化华洋化工有限公司 六磺酸类液体荧光增白剂的制备方法

Also Published As

Publication number Publication date
DK448489D0 (da) 1989-09-12
JPH02112478A (ja) 1990-04-25
DE3831093A1 (de) 1990-03-15
EP0359039A3 (fr) 1991-07-31
DK448489A (da) 1990-03-14

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