EP1063343A1 - Composition aqueuse pour l'apprêtage de matériaux fibrieux pour l'impression par transfert thermique - Google Patents
Composition aqueuse pour l'apprêtage de matériaux fibrieux pour l'impression par transfert thermique Download PDFInfo
- Publication number
- EP1063343A1 EP1063343A1 EP00103963A EP00103963A EP1063343A1 EP 1063343 A1 EP1063343 A1 EP 1063343A1 EP 00103963 A EP00103963 A EP 00103963A EP 00103963 A EP00103963 A EP 00103963A EP 1063343 A1 EP1063343 A1 EP 1063343A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- fiber material
- composition according
- composition
- transfer printing
- thermal transfer
- 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- Withdrawn
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- 239000000203 mixture Substances 0.000 title claims abstract description 49
- 239000002657 fibrous material Substances 0.000 title claims abstract description 38
- 238000010023 transfer printing Methods 0.000 title claims abstract description 24
- 238000000034 method Methods 0.000 title claims abstract description 23
- 230000008569 process Effects 0.000 title claims abstract description 17
- 229920003002 synthetic resin Polymers 0.000 claims abstract description 23
- 239000000057 synthetic resin Substances 0.000 claims abstract description 23
- 229920001169 thermoplastic Polymers 0.000 claims abstract description 21
- 239000004416 thermosoftening plastic Substances 0.000 claims abstract description 20
- 239000003995 emulsifying agent Substances 0.000 claims abstract description 8
- 239000004014 plasticizer Substances 0.000 claims abstract description 8
- 229910017053 inorganic salt Inorganic materials 0.000 claims abstract description 5
- 230000002378 acidificating effect Effects 0.000 claims abstract description 4
- -1 methylol groups Chemical group 0.000 claims description 14
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 8
- 238000004132 cross linking Methods 0.000 claims description 7
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical group [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 229920005989 resin Polymers 0.000 claims description 6
- 239000011347 resin Substances 0.000 claims description 6
- 238000007639 printing Methods 0.000 claims description 5
- 229920002545 silicone oil Polymers 0.000 claims description 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 229910001629 magnesium chloride Inorganic materials 0.000 claims description 3
- 239000012875 nonionic emulsifier Substances 0.000 claims description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical class OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 2
- 238000007651 thermal printing Methods 0.000 abstract 1
- 239000000835 fiber Substances 0.000 description 17
- 229920002678 cellulose Polymers 0.000 description 16
- 239000001913 cellulose Substances 0.000 description 16
- 239000000986 disperse dye Substances 0.000 description 16
- 239000004753 textile Substances 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 9
- 239000000463 material Substances 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 8
- 238000001035 drying Methods 0.000 description 8
- 229920001577 copolymer Polymers 0.000 description 6
- 239000001993 wax Substances 0.000 description 6
- 229920003043 Cellulose fiber Polymers 0.000 description 5
- 229920000742 Cotton Polymers 0.000 description 5
- 239000004744 fabric Substances 0.000 description 5
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 4
- 238000009833 condensation Methods 0.000 description 4
- 230000005494 condensation Effects 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 3
- 239000003431 cross linking reagent Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- WVJOGYWFVNTSAU-UHFFFAOYSA-N dimethylol ethylene urea Chemical compound OCN1CCN(CO)C1=O WVJOGYWFVNTSAU-UHFFFAOYSA-N 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000002349 favourable effect Effects 0.000 description 3
- 230000002209 hydrophobic effect Effects 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- ZEYUSQVGRCPBPG-UHFFFAOYSA-N 4,5-dihydroxy-1,3-bis(hydroxymethyl)imidazolidin-2-one Chemical compound OCN1C(O)C(O)N(CO)C1=O ZEYUSQVGRCPBPG-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- MBHRHUJRKGNOKX-UHFFFAOYSA-N [(4,6-diamino-1,3,5-triazin-2-yl)amino]methanol Chemical class NC1=NC(N)=NC(NCO)=N1 MBHRHUJRKGNOKX-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 239000004205 dimethyl polysiloxane Substances 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- YIXJRHPUWRPCBB-UHFFFAOYSA-N magnesium nitrate Chemical compound [Mg+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O YIXJRHPUWRPCBB-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 239000004627 regenerated cellulose Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000012815 thermoplastic material Substances 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- ONDPHDOFVYQSGI-UHFFFAOYSA-N zinc nitrate Chemical compound [Zn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ONDPHDOFVYQSGI-UHFFFAOYSA-N 0.000 description 2
- NQPJDJVGBDHCAD-UHFFFAOYSA-N 1,3-diazinan-2-one Chemical compound OC1=NCCCN1 NQPJDJVGBDHCAD-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- NNTWKXKLHMTGBU-UHFFFAOYSA-N 4,5-dihydroxyimidazolidin-2-one Chemical compound OC1NC(=O)NC1O NNTWKXKLHMTGBU-UHFFFAOYSA-N 0.000 description 1
- WEAJVJTWVRAPED-UHFFFAOYSA-N [[4-amino-6-[bis(hydroxymethyl)amino]-1,3,5-triazin-2-yl]-(hydroxymethyl)amino]methanol Chemical compound NC1=NC(N(CO)CO)=NC(N(CO)CO)=N1 WEAJVJTWVRAPED-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 229940015043 glyoxal Drugs 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- SXVDZIOMWSPFCO-UHFFFAOYSA-N methyl n,n-bis(hydroxymethyl)carbamate Chemical compound COC(=O)N(CO)CO SXVDZIOMWSPFCO-UHFFFAOYSA-N 0.000 description 1
- YVOQADGLLJCMOE-UHFFFAOYSA-N n-[6-(aziridine-1-carbonylamino)hexyl]aziridine-1-carboxamide Chemical compound C1CN1C(=O)NCCCCCCNC(=O)N1CC1 YVOQADGLLJCMOE-UHFFFAOYSA-N 0.000 description 1
- 230000006855 networking Effects 0.000 description 1
- QUBQYFYWUJJAAK-UHFFFAOYSA-N oxymethurea Chemical compound OCNC(=O)NCO QUBQYFYWUJJAAK-UHFFFAOYSA-N 0.000 description 1
- 229950005308 oxymethurea Drugs 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 238000007669 thermal treatment Methods 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 230000002110 toxicologic effect Effects 0.000 description 1
- 231100000027 toxicology Toxicity 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
Classifications
-
- 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
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/52—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing synthetic macromolecular substances
- D06P1/54—Substances with reactive groups together with crosslinking agents
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/52—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing synthetic macromolecular substances
- D06P1/56—Condensation products or precondensation products prepared with aldehydes
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/52—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing synthetic macromolecular substances
- D06P1/56—Condensation products or precondensation products prepared with aldehydes
- D06P1/58—Condensation products or precondensation products prepared with aldehydes together with other synthetic macromolecular substances
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P5/00—Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
- D06P5/003—Transfer printing
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/52—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing synthetic macromolecular substances
- D06P1/5207—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- D06P1/5214—Polymers of unsaturated compounds containing no COOH groups or functional derivatives thereof
- D06P1/5242—Polymers of unsaturated N-containing compounds
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/52—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing synthetic macromolecular substances
- D06P1/5207—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- D06P1/525—Polymers of unsaturated carboxylic acids or functional derivatives thereof
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/52—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing synthetic macromolecular substances
- D06P1/5207—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- D06P1/525—Polymers of unsaturated carboxylic acids or functional derivatives thereof
- D06P1/5257—(Meth)acrylic acid
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/02—Material containing basic nitrogen
- D06P3/04—Material containing basic nitrogen containing amide groups
- D06P3/14—Wool
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/58—Material containing hydroxyl groups
- D06P3/60—Natural or regenerated cellulose
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
- Y10T428/254—Polymeric or resinous material
Definitions
- the invention relates to an aqueous composition for finishing Fiber material for a thermal transfer printing process, the use of the Composition therefor and a thermal transfer printing process.
- the disperse dye is removed using a Printing paste first on a support, e.g. B. paper with a special Coating applied.
- a support e.g. B. paper with a special Coating applied.
- the one there the high temperature used favors the diffusion of the dye into the Fibers of the textile material.
- this transfer of the dye is on the textile material is carried out at 200 - 250 ° C in a few seconds.
- the thermal transfer printing process requires that the disperse dye can diffuse into the fiber.
- this is the case with natural fibers such as cotton or Wool, and not the case with regenerated cellulose fibers. These must be in first be appropriately equipped.
- German Patent 41 26 096 describes a method for Printing of substrates by means of transfer printing processes known, in which one of Resins free transparent varnish applied to the natural fibers to be printed and dried, the sublimable dyes in the subsequent Can record and fix thermal transfer printing.
- leaks are liquid or powder-proof Substances that are applied to objects in a thin layer and that by chemical reaction and / or physical change one on the Form solid film adhering to objects. It is through the formation of a film however, to an undesirable decrease in air permeability and reduced Breathability and a relatively hard grip of the textile material.
- the present invention is therefore based on the object of a means for To provide equipment for fiber material for a thermal transfer printing process, that the air permeability and breathability of the fiber material after the Pressure not undesirably reduced and the fiber material a pleasant gives a soft grip.
- aqueous composition "indicates that it contains, in addition to the components a) to e) mentioned above and, if appropriate, further customary constituents to compensate for 100% by weight of water, ie the rest is water. These constituents can be present in an amount of up to 5 % By weight, based on the composition.
- the composition according to the invention has a synthetic pre-condensate in the amount specified above.
- the treatment of cellulose fibers with synthetic resin precondensates (crosslinking agents) is a generally known method in the textile field and is described in detail in the textile technology literature. B. to H. Tovey, Textile Research Journal 31 , pages 185 to 237 (1961), H. Rath, Journal for the entire textile industry 69 , pages 542 to 548 and Rare 631 to 635 (1967) and the aforementioned Schwelzer patent .
- the synthetic resin pre-condensates can be monomeric compounds act, which may contain two or more reactive groups, these reactive groups on the one hand with cellulose, especially the OH groups of Cellulose, and on the other hand with the reactive groups React resin pre-condensate molecules to form a covalent bond can.
- the molecules of the synthetic resin condensate can thus be combined with one another react and be networked with the cellulose. Examples of reactive groups are Carbonyl, carboxyl and methylol groups.
- Examples of the synthetic resin precondensates are acetals, e.g. B. reaction products Formaldehyde and diethylene glycol, dimethylol monocarbamates, e.g. B. dimethylol methyl carbamate, Dimethylolurea, dihydroxyethyleneurea, propyleneurea and its derivatives, triazone such as dimethylol-5-methoxyethyl-1,3,5-triazinon-2, methylol-melamine compounds such as tetramethylolmelamine or water-soluble etherified Methylolmelamine compounds, hexamethylene diethylene urea and glyoxal and its derivatives.
- acetals e.g. B. reaction products Formaldehyde and diethylene glycol
- dimethylol monocarbamates e.g. B. dimethylol methyl carbamate, Dimethylolurea, dihydroxyethyleneurea, propyleneurea and its derivatives
- triazone such
- the synthetic resin precondensate can also have different reactive groups exhibit.
- the synthetic resin precondensate is preferably a compound in which there are at least two methylol groups (-CH 2 -OH) which are advantageously bound to N atoms, which are different N atoms or the same N atom can act. It is favorable that the N atom is adjacent to a carbonyl group. Examples of such N-methylol compounds are dimethylolethylene urea and compounds derived therefrom.
- the H atom of the OH group of the methylol group can be replaced by an alkyl radical, e.g. B. a C 1 -C 4 alkyl radical may be substituted. If desired, the H atoms of all or only some of the OH groups of the methylol groups can be replaced by alkyl radicals.
- Examples of the compounds derived from dimethylolethylene urea are those of the formula wherein R 'and R''are identical or different from one another and represent H and OH and R 1 and R 2 are identical or different from one another and represent H and C 1 -C 4 alkyl.
- An example of a compound of the above formula derived from dimethylolethyleneurea is dimethyloldihydroxyethyleneurea.
- Composition also exist, e.g. B. two or three from each other are different.
- thermoplastic As component b), a thermoplastic with reactive groups is present in the composition according to the invention.
- thermoplastic For the purposes of the present invention, thermoplastics of any kind are understood. These can be homopolymers or copolymers. The copolymers can be block or random copolymers. Examples of monomers which are suitable for producing the thermoplastic are Olefins such as ethylene, vinyl acetate, (meth) acrylic acid and their esters such as butyl acrylate.
- the reactive groups present in the thermoplastic are favorably those related to the Synthetic resin precondensate described reactive groups and / or the OH groups the cellulose can react, causing crosslinking of the thermoplastic Plastic with the cellulose and / or the synthetic resin precondensate can be achieved can.
- Examples of such are the carboxyl group and the methylol group, in particular the methylol groups bonded to an N atom, it being favorable when the N atom is adjacent to a carbonyl group.
- thermoplastic be introduced that during its production (polymerisation of monomers) Monomers are used which have these reactive groups, for. B. the above-mentioned N-methylolacrylamide and / or (meth) acrylic acid.
- the amount of reactive group-bearing monomers in thermoplastic is 1 to 10 wt .-%, in particular about 5 wt .-%, based on the thermoplastic.
- An example of a thermoplastic is a copolymer of ethylene and vinyl acetate (20:80 parts by weight) containing 5% by weight Methylolacrylamide.
- Another example of this is a copolymer made from vinyl acetate Acyl acid butyl ester (1: 1), contain 2.5 wt .-% Aaylic acid, based on the thermoplastic.
- thermoplastic can have several different reactive substances Have groups. Furthermore, in the composition according to the invention several, e.g. B. two different thermoplastic materials are present which, if desired, carry different reactive groups can. Are two different thermoplastics in the used composition according to the invention, their ratio can be about 1: 1 be.
- component c) there is an acid in the composition according to the invention reacting inorganic salt.
- This serves as a catalyst for cross-linking of components a) and b) with one another and with the cellulose.
- salts are diammonium sulfate, zinc nitrate, zinc chloride, magnesium nitrate and in particular Magnesium chloride.
- the latter salt is a particularly gentle system and it lower losses in the tensile strength of the fiber material are obtained.
- Component d) contains 0.2 to 2.0% by weight of a plasticizer or a mixture of several plasticizers in the composition according to the invention.
- Plasticizers are understood to mean compounds of any kind which give the fiber material a soft feel. Examples of these are hydrophobic compounds, preferably waxes, in particular. Polyethylene waxes, and silicone oils, in particular based on polydimethylsiloxane, or mixtures thereof.
- the amount of wax can be 0.1 to 1.0% by weight and that of silicone oil can also be 0.1 to 1.0% by weight, based in each case on the composition
- Combination of wax and silicone oil gives the fiber material an excellent grip in a particularly advantageous manner, but at the same time does not adversely affect the real properties of prints.
- the combination mentioned also has a positive effect in terms of the film-forming properties of the thermoplastic materials.
- composition according to the invention there is an amount of 0.05 to 0.5 % By weight of an emulsifier.
- This can be one or more act non-ionic emulsifier (s), e.g. B. Connections based ethoxylated fatty alcohols, ethoxylated fatty amines and mixtures thereof.
- s non-ionic emulsifier
- the composition of the invention is kept stable and the Application of the composition to the fiber material, in particular by Mold application, improved.
- the composition according to the invention can be used to furnish fiber material for a thermal transfer printing process can be used.
- Methods are known to the person skilled in the art for applying the compositions according to the invention to fiber material and devices required for this are known.
- the aqueous Composition applied to the fiber material by pad application become.
- the composition according to the invention with the above Components a) to e) can in one step, d. H. all at once, on the fiber material can be applied, which makes it easy, quick and inexpensive to apply of components a) to e) is possible on the fiber material.
- Fibrous material means fibers and fiber-containing materials of any kind.
- the latter can be textile fabrics made from fibers.
- the material from which the fibers or textile fabrics are made can consist of cellulose or comprise cellulose, whereby under Cellulose “is also understood to mean chemically and / or physically modified cellulose.
- Examples of the fibers are natural fibers, for example cotton or wool, and regenerated cellulose fibers.
- the invention Composition applied to fiber material
- the Amount of the composition according to the invention chosen so that it is complete can be absorbed by the fiber material, d. H. the absorption is 100%.
- drying can take place, the water being able to be substantially completely removed.
- This means essentially "that some water may still be present.
- This is usually carried out at temperatures of 100 ° C. or more (at normal pressure).
- the drying temperature should not exceed 140 ° C., since at these temperatures a condensation of the synthetic resin precondensate, possibly For example, the drying temperature is approximately 110 ° C.
- the drying time depends on how much residual water should remain in the fiber material after drying. If the residual water is to be low, the drying process is carried out for a longer time.
- the fiber material treated in this way can then be used in a conventional manner Thermal transfer printing processes are used.
- Disperse dye in particular a sublimable disperse dye
- a printing paste on a support, e.g. B. a paper with a special coating, upset.
- fiber material disperse dye present on the support from this to the fiber material transfer.
- this pattern is applied to the fiber material transfer.
- the transfer can take place at temperatures from 200 to 250 ° C in a few Seconds to a few minutes, e.g. B. 10 seconds to 2 minutes. Doing so a crosslinking of the synthetic resin precondensate, the thermoplastic and reached the cellulose.
- the specified amounts are demineralized, cold Make up to 1 liter of water and use a foulard on the cotton fabric upset.
- the fleet intake is 100%.
- the thermal transfer pressure was below at 210 ° C with a contact time of 30 seconds Use of a fiber material made of 100% cotton and a commercially available Paper carrier with disperse dyes (from Transfertex GmbH & Co. Thermobuch KG). The complete networking of the Resin precondensates were also used in this thermal treatment reached.
- the print obtained was washable.
- the cotton fabric showed that usual easy care effects, d. H. Improve the shrink properties and the Tendency to wrinkle. It had a pleasant grip.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Coloring (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19918890 | 1999-04-26 | ||
| DE19918890A DE19918890A1 (de) | 1999-04-26 | 1999-04-26 | Wäßrige Zusammensetzung zur Ausrüstung von Fasermaterial für ein Thermotransferdruckverfahren |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP1063343A1 true EP1063343A1 (fr) | 2000-12-27 |
Family
ID=7905885
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP00103963A Withdrawn EP1063343A1 (fr) | 1999-04-26 | 2000-02-25 | Composition aqueuse pour l'apprêtage de matériaux fibrieux pour l'impression par transfert thermique |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US6425927B1 (fr) |
| EP (1) | EP1063343A1 (fr) |
| KR (1) | KR20010049270A (fr) |
| DE (1) | DE19918890A1 (fr) |
| TR (1) | TR200000814A3 (fr) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2003900744A0 (en) * | 2003-01-15 | 2003-03-06 | Justoy Pty Ltd | A tow hitch arrangement |
| US7714217B2 (en) | 2007-12-21 | 2010-05-11 | Innovatech, Llc | Marked precoated strings and method of manufacturing same |
| US8231926B2 (en) | 2007-12-21 | 2012-07-31 | Innovatech, Llc | Marked precoated medical device and method of manufacturing same |
| US8231927B2 (en) | 2007-12-21 | 2012-07-31 | Innovatech, Llc | Marked precoated medical device and method of manufacturing same |
| US7811623B2 (en) | 2007-12-21 | 2010-10-12 | Innovatech, Llc | Marked precoated medical device and method of manufacturing same |
| US8048471B2 (en) | 2007-12-21 | 2011-11-01 | Innovatech, Llc | Marked precoated medical device and method of manufacturing same |
| US8900652B1 (en) | 2011-03-14 | 2014-12-02 | Innovatech, Llc | Marked fluoropolymer surfaces and method of manufacturing same |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2458660A1 (de) * | 1973-12-13 | 1975-06-19 | Sublistatic Holding Sa | Trockenthermodruckverfahren |
| CH564637B5 (fr) * | 1973-08-03 | 1975-07-31 | ||
| US4119398A (en) * | 1976-08-31 | 1978-10-10 | Terry Brook Purser | Composition for pre-treating fabric for transfer printing and a transfer printing process |
| EP0038965A1 (fr) * | 1980-04-26 | 1981-11-04 | Subligraphics S.A. | Produit et procédé de prétraitement des fibres cellulosiques à imprimer par transfert |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE222052C (fr) | ||||
| US3674548A (en) * | 1969-04-09 | 1972-07-04 | Deering Milliken Res Corp | Process for imparting soil-releasing and anti soil-redeposition properties to textile materials |
| US3776692A (en) * | 1972-04-27 | 1973-12-04 | Us Agriculture | Recurable crosslinked cellulosic fabrics from methylol reagents and polycarboxylic acids |
| US4112155A (en) * | 1974-03-11 | 1978-09-05 | Produits Chimiques Ugine Kuhlmann | Process for sizing substrate and products obtained thereby |
| DE2840438A1 (de) * | 1978-09-16 | 1980-03-27 | Hoechst Ag | Verfahren zur vorbehandlung von cellulosefasern, die nach dem thermotransferverfahren bedruckt werden |
| US4269603A (en) * | 1979-05-04 | 1981-05-26 | Riegel Textile Corporation | Non-formaldehyde durable press textile treatment |
| US4240795A (en) * | 1979-07-09 | 1980-12-23 | Sun Chemical Corporation | Treatment of textiles with modified alpha-olefins |
| JPS6036397B2 (ja) | 1980-03-31 | 1985-08-20 | 株式会社東芝 | 熱記録装置 |
| DD222052A1 (de) * | 1983-12-09 | 1985-05-08 | Flath Hans Joachim | Verfahren zum faerben von cellulosefaserstoffen und deren mischungen |
| FI78514C (fi) * | 1983-12-16 | 1989-08-10 | Sicpa Holding Sa | Transfertryckplatta, foerfarande foer dess framstaellning, trycksvaerta foer anvaendning i foerfarandet samt transfertryckningsfoerfarande foer att trycka textilunderlag medelst transfertryckplattan. |
| US4524093A (en) * | 1984-04-30 | 1985-06-18 | The B. F. Goodrich Company | Fabric coating composition with low formaldehyde evolution |
| DE3525799A1 (de) * | 1985-07-19 | 1987-01-22 | Basf Ag | Bindemittel fuer den pigmentdruck von textilgut |
| US4737386A (en) * | 1986-09-08 | 1988-04-12 | National Starch And Chemical Corporation | Textile coating composition and textiles coated therewith |
| KR910003654B1 (ko) * | 1989-06-24 | 1991-06-08 | 제일합섬 주식회사 | 내구성이 우수한 마촉감을 갖는 면직물의 제조방법 |
| DE4126096A1 (de) | 1991-08-07 | 1993-02-11 | Thomas Kerle | Verfahren zum bedrucken von substraten mittels transfer-druckverfahren |
| US5811369A (en) * | 1995-12-01 | 1998-09-22 | Nippon Paper Industries Co., Ltd. | Thermal recording medium |
| US6139672A (en) * | 1997-05-30 | 2000-10-31 | Canon Kabushiki Kaisha | Image-transfer medium for ink-jet recording and image-transfer printing process |
-
1999
- 1999-04-26 DE DE19918890A patent/DE19918890A1/de not_active Withdrawn
-
2000
- 2000-02-25 EP EP00103963A patent/EP1063343A1/fr not_active Withdrawn
- 2000-03-29 TR TR2000/00814A patent/TR200000814A3/tr unknown
- 2000-04-19 KR KR1020000020772A patent/KR20010049270A/ko not_active Ceased
- 2000-04-25 US US09/558,312 patent/US6425927B1/en not_active Expired - Fee Related
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH564637B5 (fr) * | 1973-08-03 | 1975-07-31 | ||
| DE2458660A1 (de) * | 1973-12-13 | 1975-06-19 | Sublistatic Holding Sa | Trockenthermodruckverfahren |
| US4119398A (en) * | 1976-08-31 | 1978-10-10 | Terry Brook Purser | Composition for pre-treating fabric for transfer printing and a transfer printing process |
| EP0038965A1 (fr) * | 1980-04-26 | 1981-11-04 | Subligraphics S.A. | Produit et procédé de prétraitement des fibres cellulosiques à imprimer par transfert |
Also Published As
| Publication number | Publication date |
|---|---|
| TR200000814A2 (tr) | 2000-11-21 |
| KR20010049270A (ko) | 2001-06-15 |
| US6425927B1 (en) | 2002-07-30 |
| TR200000814A3 (tr) | 2000-11-21 |
| DE19918890A1 (de) | 2000-11-02 |
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