EP0009721B1 - Process of foam-treating textile materials - Google Patents
Process of foam-treating textile materials Download PDFInfo
- Publication number
- EP0009721B1 EP0009721B1 EP19790103530 EP79103530A EP0009721B1 EP 0009721 B1 EP0009721 B1 EP 0009721B1 EP 19790103530 EP19790103530 EP 19790103530 EP 79103530 A EP79103530 A EP 79103530A EP 0009721 B1 EP0009721 B1 EP 0009721B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- composition
- foamed
- dye
- foam
- finishing agent
- 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
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- 239000004753 textile Substances 0.000 title claims description 58
- 239000000463 material Substances 0.000 title claims description 35
- 238000000034 method Methods 0.000 title claims description 33
- 230000008569 process Effects 0.000 title claims description 25
- 239000000203 mixture Substances 0.000 claims description 122
- 239000003795 chemical substances by application Substances 0.000 claims description 69
- 239000004744 fabric Substances 0.000 claims description 68
- 239000006260 foam Substances 0.000 claims description 49
- 239000007788 liquid Substances 0.000 claims description 33
- 239000000975 dye Substances 0.000 claims description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 21
- 238000001035 drying Methods 0.000 claims description 5
- 238000005187 foaming Methods 0.000 claims description 5
- 230000035515 penetration Effects 0.000 claims description 5
- 239000000985 reactive dye Substances 0.000 claims description 5
- 239000002689 soil Substances 0.000 claims description 4
- 230000002940 repellent Effects 0.000 claims description 3
- 239000005871 repellent Substances 0.000 claims description 3
- 239000003063 flame retardant Substances 0.000 claims description 2
- 239000004088 foaming agent Substances 0.000 claims description 2
- 238000004040 coloring Methods 0.000 claims 3
- 239000000758 substrate Substances 0.000 claims 1
- 238000010345 tape casting Methods 0.000 claims 1
- 239000002421 finishing Substances 0.000 description 46
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 15
- 229920000742 Cotton Polymers 0.000 description 15
- 239000000243 solution Substances 0.000 description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 239000000049 pigment Substances 0.000 description 7
- 239000006185 dispersion Substances 0.000 description 6
- 229920000728 polyester Polymers 0.000 description 6
- 239000003086 colorant Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 229940088990 ammonium stearate Drugs 0.000 description 4
- JPNZKPRONVOMLL-UHFFFAOYSA-N azane;octadecanoic acid Chemical compound [NH4+].CCCCCCCCCCCCCCCCCC([O-])=O JPNZKPRONVOMLL-UHFFFAOYSA-N 0.000 description 4
- 238000004043 dyeing Methods 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 239000011342 resin composition Substances 0.000 description 4
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
- 229920002125 Sokalan® Polymers 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 235000011114 ammonium hydroxide Nutrition 0.000 description 3
- 230000000740 bleeding effect Effects 0.000 description 3
- -1 e.g. Substances 0.000 description 3
- 239000000675 fabric finishing Substances 0.000 description 3
- 238000009962 finishing (textile) Methods 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- AVYGCQXNNJPXSS-UHFFFAOYSA-N 2,5-dichloroaniline Chemical class NC1=CC(Cl)=CC=C1Cl AVYGCQXNNJPXSS-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- 239000004908 Emulsion polymer Substances 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000000982 direct dye Substances 0.000 description 2
- 238000011010 flushing procedure Methods 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- RTLULCVBFCRQKI-UHFFFAOYSA-N 1-amino-4-[3-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-4-sulfoanilino]-9,10-dioxoanthracene-2-sulfonic acid Chemical compound C1=2C(=O)C3=CC=CC=C3C(=O)C=2C(N)=C(S(O)(=O)=O)C=C1NC(C=1)=CC=C(S(O)(=O)=O)C=1NC1=NC(Cl)=NC(Cl)=N1 RTLULCVBFCRQKI-UHFFFAOYSA-N 0.000 description 1
- MHXFWEJMQVIWDH-UHFFFAOYSA-N 1-amino-4-hydroxy-2-phenoxyanthracene-9,10-dione Chemical compound C1=C(O)C=2C(=O)C3=CC=CC=C3C(=O)C=2C(N)=C1OC1=CC=CC=C1 MHXFWEJMQVIWDH-UHFFFAOYSA-N 0.000 description 1
- JFGQHAHJWJBOPD-UHFFFAOYSA-N 3-hydroxy-n-phenylnaphthalene-2-carboxamide Chemical compound OC1=CC2=CC=CC=C2C=C1C(=O)NC1=CC=CC=C1 JFGQHAHJWJBOPD-UHFFFAOYSA-N 0.000 description 1
- VDBJCDWTNCKRTF-UHFFFAOYSA-N 6'-hydroxyspiro[2-benzofuran-3,9'-9ah-xanthene]-1,3'-dione Chemical compound O1C(=O)C2=CC=CC=C2C21C1C=CC(=O)C=C1OC1=CC(O)=CC=C21 VDBJCDWTNCKRTF-UHFFFAOYSA-N 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 1
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229920003091 Methocel™ Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 241001074085 Scophthalmus aquosus Species 0.000 description 1
- 229920006243 acrylic copolymer Polymers 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000009978 beck dyeing Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000012757 flame retardant agent Substances 0.000 description 1
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical class O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000004900 laundering Methods 0.000 description 1
- 239000006193 liquid solution Substances 0.000 description 1
- 239000006194 liquid suspension Substances 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 1
- 229910052979 sodium sulfide Inorganic materials 0.000 description 1
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
Images
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06B—TREATING TEXTILE MATERIALS USING LIQUIDS, GASES OR VAPOURS
- D06B19/00—Treatment of textile materials by liquids, gases or vapours, not provided for in groups D06B1/00 - D06B17/00
- D06B19/0088—Treatment of textile materials by liquids, gases or vapours, not provided for in groups D06B1/00 - D06B17/00 using a short bath ratio liquor
- D06B19/0094—Treatment of textile materials by liquids, gases or vapours, not provided for in groups D06B1/00 - D06B17/00 using a short bath ratio liquor as a foam
-
- 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
- D06P1/96—Dyeing characterised by a short bath ratio
- D06P1/965—Foam dyeing
Definitions
- This invention relates to textile materials and, more particularly, to the application of finishing agents to textile materials.
- the treating of textile materials with finishing agents involves a procedure wherein the finishing agent is either dissolved or dispersed in a suitable liquid medium carrier such as an aqueous or organic liquid, and then applied to the textile, such as by passing the textile through a bath or vat containing the solution or dispersion. Thereafter, the carrier is removed from the fabric, usually by evaporation with or without heat. Since only a small amount of the finishing agent is needed to achieve the desired effect, a relatively large amount of carrier (water) is used to assure uniform distribution of the finishing agent. This results in relatively large amounts of liquid medium which must be removed from the fabric. Consequently, a substantial amount of the cost incurred in such processes resides in the liquid medium removal step.
- a suitable liquid medium carrier such as an aqueous or organic liquid
- finishing agent For many textiles it is desired to apply more than one finishing agent thereto. For example, it may be desirable to first dye the textile and then apply a durable press agent or to apply both durable press and soil release agents to the textile. Since relatively few of such combinations of finishing agents can be applied together from the same medium, such multiple agents are typically applied to the textile in a serial manner. Thus, for example, a coloring agent is first applied to the textile; the textile is then dried; and the colored textile then treated with a further fabric finishing agent in a conventional manner and then re-dried.
- US-A-4099913 and FR-A-22 66 766 describe the applying of textile treating compounds using foam compositions that break immediately on contact with the textile material and are rapidly absorbed.
- a further object of the present invention is to provide a serial process for treating a textile with at least one finishing agent which does not require intermediate fixation of the textile prior to application of a foam composition thereover.
- a still further object of the present invention is to provide a process of the type mentioned which does not present difficulties in the control of the amounts of finishing agent applied to the textile.
- a textile is first treated with a finishing agent-containing composition and, without prior fixation, (i.e., complete removal of all liquid therefrom), is thereafter treated with a second covering composition which is applied in the form of a foam.
- the textile is then treated to collapse the foamed composition and effect uniform penetration of the finishing agent into the fabric.
- the treatment of textiles in accordance with the present invention has the advantage of eliminating costly liquid removal procedures between application of finishing agents. Moreover, it has been found that application of the second finishing agent in the subsequently applied foamed composition avoids the earlier- referred to dilution effect arising from conventional application of the second finishing agent in a liquid solution or suspension since significantly less liquid per se is required when such compositions are applied as foams, and since the foam can be applied without the need for passing the textile through a bath or vat containing the liquid finishing agent composition.
- the application of the first finishing agent-containing composition to the textile can be accomplished in accordance with conventional techniques, e.g., by continuously passing the textile through a bath or vat containing the liquid composition.
- the first finishing agent composition may be applied in the form of a foam. In this method of operation, this first foam applied to the textile is collapsed, prior to application of the second foamed composition to the textile. Such collapsing of the first applied foam may occur upon application such as when using rotary screen printers and the like.
- Finishing agent-containing compositions for utilization in the present invention are known in the art and typically comprise a finishing agent and an aqueous or organic liquid carrier medium along with other known, optional ingredients.
- finishing agents which may be utilized in the treatment of textiles according to the present invention include coloring agents, dyes, pigments, durable press agents, soil release agents, weighting agents, flame retardants, water repellents, softeners, and the like.
- Foamable, liquid compositions containing such finishing agents, and methods of preparing foams therefrom, are known in the art.
- the application of the first finishing agent-containing composition may comprise printing the textile with a pre-selected pattern in accordance with known procedures, e.g., by use of an intaglio printing cylinder or a rotary screen printer.
- the first composition may be a conventional liquid printing composition, a foamed printing composition or a powdered composition.
- a foamed composition, with another finishing agent is applied to the textile prior to fixation of the first applied finishing agent to the printed textile.
- the process of the present invention will typically be utilized for the serial application of two or more differing types of finishing agents to a textile, e.g., a colorant and a water- repellent or a colorant and a durable press agent, although numerous other combinations exist.
- finishing agents e.g., a colorant and a water- repellent or a colorant and a durable press agent, although numerous other combinations exist.
- textile material is intended to include, without limitation, fabrics made from threads, yarns, woven or knitted goods, resin bonded mats of fibres, and the like.
- the second, serially applied fabric finishing agent is applied to the textile in the form of a foam while the textile still contains a first finishing agent-containing composition (either foam, liquid or powder).
- a first finishing agent-containing composition either foam, liquid or powder.
- some liquid may be removed by virtue of passage of the textile through conventional squeeze rolls prior to passing to the second serial application step.
- the generally preferred manner of collapsing the foam is accomplished by the printing screen or print roller at the instant the foam is applied to the fabric.
- the textile to which the second finishing agent composition is applied will have about 10 to 65% liquid, by weight, associated therewith.
- a roll of fabric 10 travelling in the direction indicated by the arrow, is passed by suitable conveying means to a bath 12 containing a pre-prepared liquid e.g., aqueous or organic liquid, solution or dispersion containing an appropriate finishing agent, e.g., a dye material to color the fabric.
- the dyed fabric is then passed through squeeze or compression rollers 14 and 16 which serve to remove some of the liquid contained in the fabric by virtue of its passage through the solution or dispersion. Without any further liquid removal, i.e., before complete drying, the dyed fabric is coated with a foamed finishing agent composition.
- a foamable liquid composition comprised of liquid, foaming agent and finishing agent, e.g. a durable press agent, is formed into a foam in foamer 18.
- Foamer 18 may be any type foaming device conventionally utilized in the art, e.g., Oakes, Godwin card, Kitchenaid, etc.
- the foamed composition is transferred through line 22 by pump 20 to knife 24. At this point the foamed composition is coated onto the dyed fabric to produce a coated fabric 26.
- the coated fabric 26 then goes through nip rollers 28 and 30 to compress and collapse the foam and achieve penetration of finishing agent into the fabric. Such foam collapse may also be achieved by the application of vacuum, or a combination of vacuum and padding.
- the impregnated fabric is conveyed through a fixation means 32 which may be any of those conventionally known in the art.
- the fixed fabric is then wound on to take-up roll 34.
- FIG. 2 An alternative embodiment of the process of the present invention is shown in Fig. 2.
- a roll of fabric 40 travelling in the direction of the arrow by suitable conveying means, is coated with a first foamed fabric finishing agent composition.
- a foamed composition is prepared by foaming a suitable composition, e.g., a dye- containing foamable composition, in foamer 42.
- the foamed composition is pumped by pump 44 through line 46 to a rotary printing screen 48 at which a predetermined pattern is applied to the fabric.
- a rotary printing screen 48 As mentioned previously, with such a printing screen, the foam is caused to collapse upon application. If a procedure is employed in which the foam is not collapsed upon application, the so-coated fabric 50 is then passed over vacuum or padding device 56 or a combination of the two which serves to collapse the foam but which does not effect liquid removal from the fabric.
- the so treated fabric 66 is then coated with a second foamed finishing agent composition, formed by foaming a suitable composition, e.g., a durable press-containing foamable composition, in foamer 58.
- the second foamed composition is transferred by pump 60 through line 62 to knife 64 where it is coated on the fabric.
- the so-coated fabric 68 is then padded by passing through nip rollers 70 and 72 to collapse the foam and deeply penetrate the finishing agent into the fabric.
- the fabric is then conveyed to a fixation means 74 and wound on take-up roll 76.
- a foamable durable press resin composition was prepared containing 52.10% water, 0.62% Methocel J-75MS@ (an etherified hydroxyethyl cellulose), 1.37% Unamide N-72-3@ (a coconut alkanolamide from Lonza Chem. Co.), 36.16% Valrez-248@ (a modified glyoxal resin) and 9.8% Valcat No. 7@ (a magnesium chloride catalyst).
- This composition was foamed to a blow ratio of 9:1 and knife coated to a thickness of 0,15 mm on the wet printed samples previously prepared as described above. The fabric samples were then vacuumed, dried and cured at 177°C.
- the definition of the prints was excellent and the fabrics possessed durable press properties tested after repeated laundering.
- the print exhibited severe flushing and loss of definition so as to make the fabric commercially unacceptable. There was also some transfer of color to the pad bath.
- the foamable durable press resin composition described in Example I was foamed to a blow ratio of 8:1 and knife-coated to a thickness of 0,15 mm onto 100% cotton and 50/50 polyester/cotton blend fabrics.
- the fabrics were vacuumed and, while wet, were printed utilizing the foamed pigment composition and conditions described in
- the dye foam was coated to a thickness of 0,51 mm and the coated fabric pulled over a vacuum (wet pick-up 45%).
- the durable press foam composition was knife-coated to a thickness of 0,64 mm. The fabric was then vacuumed (total wet pick-up 62%), and dried and cured at 166°C for 3 minutes.
- the fabric contained good durable press properties and was uniformly dyed.
- a sample of the wet foam dyed fabric was also passed through a conventional finishing bath consisting of Valrez-248@, Valsof PE-19® and Valcat No. 7@ in the same ratio as the foam finishing composition but at an 8% solids concentration. Thers was significant bleeding of color into the pad bath causing the fabric to be off-shade.
- Example III The durable press resin composition of Example III was foamed to a blow ratio of 10:1 and coated to a thickness of 0,64 mm onto the wet beck-dyed fabric. The fabric was then padded at 2,4 bar, dried at 104°C and cured at 166°C for 3 minutes.
- the fabric possessed durable press properties and was uniformly dyed.
- a foamable disperse dye composition containing 2% Resolin Brill. Yellow 7 GL@ in 98% of a composition containing 0.75% QP-52000@, 1.5% Unamide N-72-3@ and 97.75% water (adjusted to a pH of 5.5 with acetic acid) was prepared anf foamed to a blow ratio of 8:1.
- This foamed composition was then knife coated to a thickness of 0,89 mm on a polyester double knit fabric. The fabric was then passed over a vacuum slot.
- a second foamable composition containing 2% Resolin Red FB@ (Disperse Red-60) in 98% of a composition containing 0,75% QP-52000@, 1.5% Unamide N-72-3@, and 97.75% water (adjusted to pH 5.5) is foamed to a blow ratio of 3:1 and over printed through a 50 mesh rotary screen printer on the wet foam- dye applied polyester knit.
- the knit fabric is then dried and thermosoled at 177°C for color fixation to produce special over printing effects.
- a foamable composition containing 4 parts Rapidogen Red KB@, 1 part caustic (50% soln.) and 95 parts of an alkaline foamable composition containing 3.5% 309-70 acrylic, 90.5% water, 0.5% ammonia and 5.5% 309-59 ammonium stearate (20% soln.) was foamed to a blow ratio of 8:1 and knife coated to a thickness of 0,64 mm on a cotton sheeting sample. The coated sample was then padded at 2,1 bar (wet pick-up 40%). A second sample was foam printed through a 50 mesh rotary screen printer with the same foam.
- An acid color developing foam was prepared by dissolving 2 parts acetic acid and 2 parts formic acid in 96 parts of a foamable composition containing 1.5 parts Unamide N-72-3@, 0.75 parts QP-52000@ and 97.75 parts water, and foaming to a 10:1 blow ratio.
- This foamed composition was coated to a thickness of 0,64 mm onto each of the above-referred to wet samples. The samples were then vacuumed from the back to collapse the foam and then steamed at 99°C to remove acid vapor and water. The color was developed and demonstrated good fixation.
- the printed fabric had excellent definition.
- a foamable prewetting composition containing 0.5 parts Valdet 4016@ and 94.5 parts water was prepared.
- the composition was foamed to a 10:1 blow ratio and 0,64 mm of foam was coated on a cotton velour upholstery material and padded.
- direct dye foam was applied as follows:
- a 10% solution of procion Red MX 5B@ reactive dye in water was prepared.
- the dye solution was applied to a cotton carpet pile in a random pattern.
- the sample was wet stored for 4 hrs. and dried at 104°C.
- the randomly applied color had good penetration inside pile.
- a foamable composition consisting of 3.5 parts of Valthick-70@ (an acrylic acid emulsion polymer), 0.5 parts of aqua ammonia, 5.5 parts of a 20% solution of ammonium stearate and 90.5 parts of water was prepared.
- a second foamable composition consisting of 1.5 parts of Valdet CC@ (a fatty acid diethanolamide manufactured by Valchem), 0.75 parts of Cellosize QP 52000@ (a hydroxyethyl cellulose manufactured by Union Carbide) and 97.75 parts of water was prepared.
- Valdet CC@ a fatty acid diethanolamide manufactured by Valchem
- Cellosize QP 52000@ a hydroxyethyl cellulose manufactured by Union Carbide
- this second foamable composition was added 8 parts of Fast Scarlet 2G@ salt (C.I. Azoic Diazo Component 3) and 2 parts of acetic acid.
- the composition was mechanically foamed to an 8 to 1 blow ratio and a 0,25 mm coating was applied to the wet fabric samples previously coated with the first composition. The sample was padded at 2,1 bar and exposed to air for 3 minutes.
- the fabric was then dried.
- the dried fabric was soaped to remove the uncoupled components. Good color development was achieved.
- a first foamable composition consisting of 3.5 parts of Acrysol ASE-60® (an acrylic acid emulsion polymer manufactured by Rohm and Haas), 0.5 parts of aqua ammonia, 5.8 parts of a 20% solution of ammonium stearate and 90.2 parts of water was prepared.
- Sodyesul Liquid Blue 4BGCF@ C. I. Leuco Sulfur Blue 13
- Sodified B@ a solution of sodium sulfide manufactured by Southern Dyestuff Company
- the composition was mechanically foamed to a 6 to 1 blow ratio. 1,27 mm of the foamed composition was then knife coated onto a cotton corduroy fabric. The coated fabric was passed over a vacuum slot and then padded at 2,1 bar.
- a second fabric sample was coated with 0,64 mm of the foamed composition and padded only.
- a foamable oxidizing composition consisting of 1 part of Valdet CC@, 1 part of acetic acid, 1 part of 35% hydrogen peroxide solution and 97 parts of water was prepared. This composition was foamed to a 10 to 1 blow ratio and 5,1 mm of the foam was knife coated onto the previously wet steamed samples. The thus coated fabric samples were passed over a vacuum slot to draw the foam into the fabric. The dye was oxidized.
- a foamable vat pigment composition consisting of 96 parts of the first foamable composition described in Example X and 4 parts of Vat Yellow 4@ paste (manufactured by Ciba Geigy) was prepared.
- composition was foamed to an 8 to 1 blow ratio and then knife coated to a thickness of 0,64 mm onto cotton sheeting.
- the coated fabric was then padded and dried.
- a second foamable reducing composition was prepared from 5 parts of 50% sodium hydroxide solution, 3 parts of sodium hydrosulfite, 2 parts of Valdet CC@ and 90 parts of water. This composition was then mechanically foamed to an 8 to 1 blow ratio and a 2,54 mm coating applied to the previous vat pigment coated fabric. The fabric was then passed over a vacuum slot and steamed at 99°C for 5 minutes for reduction of vat pigment.
- the wet steamed fabric was then oxidized to develop and fix the color by applying the foamed oxidizing composition previously described in Example X.
- the fabric was then dried. A level dyeing with good fastness properties was obtained.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Coloring (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
- This invention relates to textile materials and, more particularly, to the application of finishing agents to textile materials.
- Conventionally, the treating of textile materials with finishing agents, e.g., coloring agents or dyes, resins, softeners, flame retardant agents, soil release agents and the like involves a procedure wherein the finishing agent is either dissolved or dispersed in a suitable liquid medium carrier such as an aqueous or organic liquid, and then applied to the textile, such as by passing the textile through a bath or vat containing the solution or dispersion. Thereafter, the carrier is removed from the fabric, usually by evaporation with or without heat. Since only a small amount of the finishing agent is needed to achieve the desired effect, a relatively large amount of carrier (water) is used to assure uniform distribution of the finishing agent. This results in relatively large amounts of liquid medium which must be removed from the fabric. Consequently, a substantial amount of the cost incurred in such processes resides in the liquid medium removal step.
- For many textiles it is desired to apply more than one finishing agent thereto. For example, it may be desirable to first dye the textile and then apply a durable press agent or to apply both durable press and soil release agents to the textile. Since relatively few of such combinations of finishing agents can be applied together from the same medium, such multiple agents are typically applied to the textile in a serial manner. Thus, for example, a coloring agent is first applied to the textile; the textile is then dried; and the colored textile then treated with a further fabric finishing agent in a conventional manner and then re-dried.
- In the foregoing process, the disadvantages earlier described as being associated'with the conventional utilization of large quantities of liquid medium in the application of finishing agents are necessarily multiplied. In an effort to avoid the difficulties involved with large amounts of liquid and the high cost of liquid removal processes, it has been attempted to conduct the serial application of finishing agents to a textile without intermediate drying of the textile after each application. However, this manner of operation itself leads to serious problems. Thus, when the wet textile to which a first finishing agent solution or dispersion has been applied is brought into contact with a second liquid finishing agent composition, e.g., when the wet textile is passed through a bath thereof, the liquid associated with the textile from the first application serves to dilute or otherwise alter the composition of the second finishing agent solution or dispersion. It is thereby nearly impossible to accurately control the application of specified quantities of the second finishing agent to the textile, even with the utilization of complicated measuring devices and bath replenishment techniques.
- US-A-4099913 and FR-A-22 66 766 describe the applying of textile treating compounds using foam compositions that break immediately on contact with the textile material and are rapidly absorbed.
- It is accordingly an object of the present invention to provide a process for treating a textile with more than one finishing agent.
- A further object of the present invention is to provide a serial process for treating a textile with at least one finishing agent which does not require intermediate fixation of the textile prior to application of a foam composition thereover.
- A still further object of the present invention is to provide a process of the type mentioned which does not present difficulties in the control of the amounts of finishing agent applied to the textile.
- These and other objects are achieved by the provision of a process wherein a textile is first treated with a finishing agent-containing composition and, without prior fixation, (i.e., complete removal of all liquid therefrom), is thereafter treated with a second covering composition which is applied in the form of a foam. The textile is then treated to collapse the foamed composition and effect uniform penetration of the finishing agent into the fabric.
- The treatment of textiles in accordance with the present invention has the advantage of eliminating costly liquid removal procedures between application of finishing agents. Moreover, it has been found that application of the second finishing agent in the subsequently applied foamed composition avoids the earlier- referred to dilution effect arising from conventional application of the second finishing agent in a liquid solution or suspension since significantly less liquid per se is required when such compositions are applied as foams, and since the foam can be applied without the need for passing the textile through a bath or vat containing the liquid finishing agent composition.
- In accordance with the present invention, the application of the first finishing agent-containing composition to the textile can be accomplished in accordance with conventional techniques, e.g., by continuously passing the textile through a bath or vat containing the liquid composition. However, according to a preferred embodiment of this invention, the first finishing agent composition may be applied in the form of a foam. In this method of operation, this first foam applied to the textile is collapsed, prior to application of the second foamed composition to the textile. Such collapsing of the first applied foam may occur upon application such as when using rotary screen printers and the like.
- Finishing agent-containing compositions for utilization in the present invention are known in the art and typically comprise a finishing agent and an aqueous or organic liquid carrier medium along with other known, optional ingredients.
- The various finishing agents which may be utilized in the treatment of textiles according to the present invention include coloring agents, dyes, pigments, durable press agents, soil release agents, weighting agents, flame retardants, water repellents, softeners, and the like. Foamable, liquid compositions containing such finishing agents, and methods of preparing foams therefrom, are known in the art.
- In specific embodiments of the present invention, the application of the first finishing agent-containing composition may comprise printing the textile with a pre-selected pattern in accordance with known procedures, e.g., by use of an intaglio printing cylinder or a rotary screen printer. The first composition may be a conventional liquid printing composition, a foamed printing composition or a powdered composition. After application, a foamed composition, with another finishing agent, is applied to the textile prior to fixation of the first applied finishing agent to the printed textile.
- The process of the present invention will typically be utilized for the serial application of two or more differing types of finishing agents to a textile, e.g., a colorant and a water- repellent or a colorant and a durable press agent, although numerous other combinations exist.
- As utilized herein, textile material is intended to include, without limitation, fabrics made from threads, yarns, woven or knitted goods, resin bonded mats of fibres, and the like.
- According to this invention, the second, serially applied fabric finishing agent is applied to the textile in the form of a foam while the textile still contains a first finishing agent-containing composition (either foam, liquid or powder). Thus, as utilized herein, application of the second composition without prior fixation of the textile is intended to describe and embrace processes wherein the textile has not been fully dried after application of the first composition. Hence, it is possible according to this invention that varying degrees of liquid removal, short of complete or near-complete drying, from the textile can be performed before application of the second, foamed composition, although the economic advantages of the present invention necessarily decrease in proportion to the degree of such an intermediate liquid removal step. Moreover, a certain degree of liquid removal from the textile may occur simply as a result of normal processing prior to application of the second, foamed composition. For example, some liquid may be removed by virtue of passage of the textile through conventional squeeze rolls prior to passing to the second serial application step. In the case of foam printing, the generally preferred manner of collapsing the foam is accomplished by the printing screen or print roller at the instant the foam is applied to the fabric.
- In general, the textile to which the second finishing agent composition is applied will have about 10 to 65% liquid, by weight, associated therewith.
-
- Fig. 1 is a schematic representation of an embodiment depicting the process of the present invention wherein the first liquid and finishing agent-containing composition is applied as a solution or dispersion.
- Fig. 2 is a schematic representation of an embodiment of the present invention wherein the first finishing agent-containing composition is applied in the form of a foam.
- The present invention is more fully described with reference to the description of the drawings and the Examples which follow.
- With reference to Fig. 1, a roll of
fabric 10, travelling in the direction indicated by the arrow, is passed by suitable conveying means to abath 12 containing a pre-prepared liquid e.g., aqueous or organic liquid, solution or dispersion containing an appropriate finishing agent, e.g., a dye material to color the fabric. The dyed fabric is then passed through squeeze orcompression rollers foamer 18.Foamer 18 may be any type foaming device conventionally utilized in the art, e.g., Oakes, Godwin card, Kitchenaid, etc. - The foamed composition is transferred through line 22 by
pump 20 toknife 24. At this point the foamed composition is coated onto the dyed fabric to produce a coatedfabric 26. The coatedfabric 26 then goes throughnip rollers roll 34. - An alternative embodiment of the process of the present invention is shown in Fig. 2. A roll of
fabric 40, travelling in the direction of the arrow by suitable conveying means, is coated with a first foamed fabric finishing agent composition. Such a foamed composition is prepared by foaming a suitable composition, e.g., a dye- containing foamable composition, infoamer 42. The foamed composition is pumped by pump 44 throughline 46 to arotary printing screen 48 at which a predetermined pattern is applied to the fabric. As mentioned previously, with such a printing screen, the foam is caused to collapse upon application. If a procedure is employed in which the foam is not collapsed upon application, the so-coatedfabric 50 is then passed over vacuum orpadding device 56 or a combination of the two which serves to collapse the foam but which does not effect liquid removal from the fabric. - The so treated
fabric 66 is then coated with a second foamed finishing agent composition, formed by foaming a suitable composition, e.g., a durable press-containing foamable composition, infoamer 58. The second foamed composition is transferred bypump 60 throughline 62 to knife 64 where it is coated on the fabric. The so-coatedfabric 68 is then padded by passing through niprollers up roll 76. - The following Examples illustrate various specific features of the process of the present invention.
- A foamable pigment composition containing 70.86% water, 2.07% ammonium stearate, 0.78% lauryl alcohol, 4.29% Acrysol ASE-60@ (an acrylic polymer emulsion having 28% solids (Rohm & Haas Co.)), 2% Valmel-45® (a methylolated melamine), 10% Valbond-6063@ (an acrylic copolymer emulsion) and 10% Questral Blue 3G@ (phthalocyanine pigment) was foamed to a 3:1 blow ratio and printed through a 50 mesh rotary screen on 100% cotton print cloth and 50/50 polyester/cotton blend sheeting samples. The printing foam was collapsed by the action of the screen upon application of the foam to the fabric.
- A foamable durable press resin composition was prepared containing 52.10% water, 0.62% Methocel J-75MS@ (an etherified hydroxyethyl cellulose), 1.37% Unamide N-72-3@ (a coconut alkanolamide from Lonza Chem. Co.), 36.16% Valrez-248@ (a modified glyoxal resin) and 9.8% Valcat No. 7@ (a magnesium chloride catalyst). This composition was foamed to a blow ratio of 9:1 and knife coated to a thickness of 0,15 mm on the wet printed samples previously prepared as described above. The fabric samples were then vacuumed, dried and cured at 177°C.
- The definition of the prints was excellent and the fabrics possessed durable press properties tested after repeated laundering.
- As a control, a sample of the previously described foam printed 100% cotton was passed through a conventional finishing bath of Valrez-248@ and Valcat No. 7@ and nipped through a vertical pad. The fabric was dried and cured as before.
- The print exhibited severe flushing and loss of definition so as to make the fabric commercially unacceptable. There was also some transfer of color to the pad bath.
- The foamable durable press resin composition described in Example I was foamed to a blow ratio of 8:1 and knife-coated to a thickness of 0,15 mm onto 100% cotton and 50/50 polyester/cotton blend fabrics. The fabrics were vacuumed and, while wet, were printed utilizing the foamed pigment composition and conditions described in
- Good print definitions and durable press properties were obtained.
- A foamable composition containing 2% Resolin Blue FBL@ (disperse), 1% Procion Blue HA@ (reactive), 1% sodium bicarbonate and 96% of a foamable composition containing 97.75% water, 0.75% QP-52000@ (hydroxethyl cellulose thickener from Union Carbide) and 1.5% Unamide N-72-3@ was prepared and foamed to a blow ratio of 10:1.
- A second durable press resin composition containing 50.75% water, 0.75% QP-52000@, 35% Vairez-248@, 3% Valsof PE-19@ (a polyethylene emulsion), 1% Unamide N-72-3@ and 9.5% Valcat No. 7@ was also foamed to a blow ratio of 10:1.
- On a 65/35 polyester/cotton blend fabric, the dye foam was coated to a thickness of 0,51 mm and the coated fabric pulled over a vacuum (wet pick-up 45%). On the dye-applied wet fabric, the durable press foam composition was knife-coated to a thickness of 0,64 mm. The fabric was then vacuumed (total wet pick-up 62%), and dried and cured at 166°C for 3 minutes.
- The fabric contained good durable press properties and was uniformly dyed.
- A sample of the wet foam dyed fabric was also passed through a conventional finishing bath consisting of Valrez-248@, Valsof PE-19® and Valcat No. 7@ in the same ratio as the foam finishing composition but at an 8% solids concentration. Thers was significant bleeding of color into the pad bath causing the fabric to be off-shade.
- A sample of 65/35 polyester/cotton blend was dyed, using the beck dyeing procedure, with 1% Sirius Supra Blue BRL@ (direct dye) and 2% Resolin Blue FBL@ (disperse) based on the weight of the fabric. After the dyeing cycle, the fabric was rinsed, padded and vacuumed.
- The durable press resin composition of Example III was foamed to a blow ratio of 10:1 and coated to a thickness of 0,64 mm onto the wet beck-dyed fabric. The fabric was then padded at 2,4 bar, dried at 104°C and cured at 166°C for 3 minutes.
- The fabric possessed durable press properties and was uniformly dyed.
- As a control, a sample of the wet dyed fabric was passed through a conventional finishing bath of the composition described in Example III. Again there was bleeding of the color from the fabric into the pad bath.
- A foamable disperse dye composition containing 2% Resolin Brill. Yellow 7 GL@ in 98% of a composition containing 0.75% QP-52000@, 1.5% Unamide N-72-3@ and 97.75% water (adjusted to a pH of 5.5 with acetic acid) was prepared anf foamed to a blow ratio of 8:1. This foamed composition was then knife coated to a thickness of 0,89 mm on a polyester double knit fabric. The fabric was then passed over a vacuum slot.
- A second foamable composition containing 2% Resolin Red FB@ (Disperse Red-60) in 98% of a composition containing 0,75% QP-52000@, 1.5% Unamide N-72-3@, and 97.75% water (adjusted to pH 5.5) is foamed to a blow ratio of 3:1 and over printed through a 50 mesh rotary screen printer on the wet foam- dye applied polyester knit. The knit fabric is then dried and thermosoled at 177°C for color fixation to produce special over printing effects.
- A foamable composition containing 4 parts Rapidogen Red KB@, 1 part caustic (50% soln.) and 95 parts of an alkaline foamable composition containing 3.5% 309-70 acrylic, 90.5% water, 0.5% ammonia and 5.5% 309-59 ammonium stearate (20% soln.) was foamed to a blow ratio of 8:1 and knife coated to a thickness of 0,64 mm on a cotton sheeting sample. The coated sample was then padded at 2,1 bar (wet pick-up 40%). A second sample was foam printed through a 50 mesh rotary screen printer with the same foam.
- An acid color developing foam was prepared by dissolving 2 parts acetic acid and 2 parts formic acid in 96 parts of a foamable composition containing 1.5 parts Unamide N-72-3@, 0.75 parts QP-52000@ and 97.75 parts water, and foaming to a 10:1 blow ratio. This foamed composition was coated to a thickness of 0,64 mm onto each of the above-referred to wet samples. The samples were then vacuumed from the back to collapse the foam and then steamed at 99°C to remove acid vapor and water. The color was developed and demonstrated good fixation. The printed fabric had excellent definition.
- When the printed wet samples were developed by conventional padding through a formic/acetic acid mixture, there was color bleeding and the resulting prints had flushing.
- A foamable prewetting composition containing 0.5 parts Valdet 4016@ and 94.5 parts water was prepared. The composition was foamed to a 10:1 blow ratio and 0,64 mm of foam was coated on a cotton velour upholstery material and padded. On the prewetted material direct dye foam was applied as follows:
- A dye composition containing 1 part direct dye-Sirius Supra Blue 2RL@ and 99 parts of a mix containing 3.5% Valthick-70@, 0.5% aqua ammonia, 90.5% water and 5.5% Am. stearate (20%) was foamed to 6:1 blow ratio. Then 1,27 mm of the foam was coated wet-on-wet on the foam prewetted sample and the so treated sample was vacuumed and padded. The sample was then steamed for 7 minutes at 99°C and dried at 104°C.
- Uniform dyeings were obtained on the cotton fabric having good color fastness.
- A 10% solution of procion Red MX 5B@ reactive dye in water was prepared. The dye solution was applied to a cotton carpet pile in a random pattern.
- An alkaline composition containing 2 parts sodium hydroxide (50% soln.) and 98 parts of a mix containing 3.5% Valthick-70@ (an acrylic acid polymer emulsion), 0.5% ammonia, 90.5% water and 5.5% Am. stearate (20%) was prepared. This composition was foamed to a 6:1 blow ratio and 1,27 mm of foam was knife coated on the aforementioned carpet pile having reactive dye applied. The carpet was vacuumed from the back side and padded.
- Then for reactive dye fixation, the sample was wet stored for 4 hrs. and dried at 104°C. The randomly applied color had good penetration inside pile.
- A foamable composition consisting of 3.5 parts of Valthick-70@ (an acrylic acid emulsion polymer), 0.5 parts of aqua ammonia, 5.5 parts of a 20% solution of ammonium stearate and 90.5 parts of water was prepared.
- To 95 parts of this foamable composition was added 3 parts Naphthol AS@ (C.I. Azoic Coupling component 2) and 2 parts of 50% sodium hydroxide. This mixture was mechanically foamed to an 8 to 1 blow ratio and knife coated onto cotton print cloth to a thickness of 0,25 mm. The fabric was then padded at 2,1 bar.
- A second foamable composition consisting of 1.5 parts of Valdet CC@ (a fatty acid diethanolamide manufactured by Valchem), 0.75 parts of Cellosize QP 52000@ (a hydroxyethyl cellulose manufactured by Union Carbide) and 97.75 parts of water was prepared.
- To 90 parts of this second foamable composition was added 8 parts of Fast Scarlet 2G@ salt (C.I. Azoic Diazo Component 3) and 2 parts of acetic acid. The composition was mechanically foamed to an 8 to 1 blow ratio and a 0,25 mm coating was applied to the wet fabric samples previously coated with the first composition. The sample was padded at 2,1 bar and exposed to air for 3 minutes.
- The fabric was then dried. The dried fabric was soaped to remove the uncoupled components. Good color development was achieved.
- A first foamable composition consisting of 3.5 parts of Acrysol ASE-60® (an acrylic acid emulsion polymer manufactured by Rohm and Haas), 0.5 parts of aqua ammonia, 5.8 parts of a 20% solution of ammonium stearate and 90.2 parts of water was prepared.
- To 100 parts of the foamable composition was added 6 parts of Sodyesul Liquid Blue 4BGCF@ (C. I. Leuco Sulfur Blue 13) and 6 parts of Sodified B@ (a solution of sodium sulfide manufactured by Southern Dyestuff Company) and 3 parts of soda ash.
- The composition was mechanically foamed to a 6 to 1 blow ratio. 1,27 mm of the foamed composition was then knife coated onto a cotton corduroy fabric. The coated fabric was passed over a vacuum slot and then padded at 2,1 bar.
- A second fabric sample was coated with 0,64 mm of the foamed composition and padded only.
- Both samples were steamed at 99°C for 5 minutes.
- A foamable oxidizing composition consisting of 1 part of Valdet CC@, 1 part of acetic acid, 1 part of 35% hydrogen peroxide solution and 97 parts of water was prepared. This composition was foamed to a 10 to 1 blow ratio and 5,1 mm of the foam was knife coated onto the previously wet steamed samples. The thus coated fabric samples were passed over a vacuum slot to draw the foam into the fabric. The dye was oxidized.
- The samples were then dried. The sulfur dyed cotton corduroys possessed level dyeing and good color fastness properties.
- A foamable vat pigment composition consisting of 96 parts of the first foamable composition described in Example X and 4 parts of Vat Yellow 4@ paste (manufactured by Ciba Geigy) was prepared.
- The composition was foamed to an 8 to 1 blow ratio and then knife coated to a thickness of 0,64 mm onto cotton sheeting. The coated fabric was then padded and dried.
- A second foamable reducing composition was prepared from 5 parts of 50% sodium hydroxide solution, 3 parts of sodium hydrosulfite, 2 parts of Valdet CC@ and 90 parts of water. This composition was then mechanically foamed to an 8 to 1 blow ratio and a 2,54 mm coating applied to the previous vat pigment coated fabric. The fabric was then passed over a vacuum slot and steamed at 99°C for 5 minutes for reduction of vat pigment.
- The wet steamed fabric was then oxidized to develop and fix the color by applying the foamed oxidizing composition previously described in Example X. The fabric was then dried. A level dyeing with good fastness properties was obtained.
Claims (14)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US94382978A | 1978-09-19 | 1978-09-19 | |
US943829 | 1992-09-11 |
Publications (2)
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EP0009721A1 EP0009721A1 (en) | 1980-04-16 |
EP0009721B1 true EP0009721B1 (en) | 1983-07-27 |
Family
ID=25480341
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP19790103530 Expired EP0009721B1 (en) | 1978-09-19 | 1979-09-19 | Process of foam-treating textile materials |
Country Status (8)
Country | Link |
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EP (1) | EP0009721B1 (en) |
JP (1) | JPS55500762A (en) |
AU (1) | AU525522B2 (en) |
BR (1) | BR7905992A (en) |
CA (1) | CA1132762A (en) |
GB (1) | GB2051885B (en) |
SE (1) | SE8003726L (en) |
WO (1) | WO1980000545A1 (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0030919B1 (en) * | 1979-12-14 | 1983-08-17 | Ciba-Geigy Ag | Process for the improvement, especially dyeing, optical brightening or finishing of fibrous textile materials |
DE3020668C2 (en) * | 1980-05-30 | 1984-03-08 | Küsters, Eduard, 4150 Krefeld | Method of treating a web with foam |
EP0048348A1 (en) * | 1980-09-16 | 1982-03-31 | Ramisch Kleinewefers GmbH | Method and apparatus for the regular coating of sheet-like materials with liquids, liquors or pastes |
FR2498214A1 (en) * | 1981-01-19 | 1982-07-23 | Protex Manuf Prod Chimiq | Applying foam contg. additives e.g. dyes on e.g. textile fabric - using rotary printing frame into which the foam is injected |
EP0058139B1 (en) * | 1981-02-11 | 1985-08-28 | Ciba-Geigy Ag | Process for dyeing or finishing fibrous textile materials |
DE3301607A1 (en) * | 1983-01-19 | 1984-07-26 | Mathias 4815 Schloss Holte Mitter | METHOD AND DEVICE FOR TREATING, PRINTING OR COLORING GOODS |
EP0162018B1 (en) * | 1984-05-18 | 1988-06-29 | Ciba-Geigy Ag | Process for dyeing or printing fabrics containing cellulose with vat dyes |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2971458A (en) * | 1957-12-30 | 1961-02-14 | Interchem Corp | Process of coloring textile materials |
US3030232A (en) * | 1958-02-17 | 1962-04-17 | Morgenstern David | Surface decoration of sheet material |
GB1134221A (en) * | 1965-01-29 | 1968-11-20 | Courtaulds Ltd | Improvements in and relating to the dyeing of pile fabrics |
US3762860A (en) * | 1971-05-27 | 1973-10-02 | Dexter Chemical Corp | Foam dyeing process |
US3990840A (en) * | 1972-03-24 | 1976-11-09 | Hoechst Aktiengesellschaft | Process and device for the dyeing and/or finishing of textile plane articles |
US3969780A (en) * | 1972-05-04 | 1976-07-20 | Henderson James M | Continuous carpet dyeing process |
US3954404A (en) * | 1972-06-22 | 1976-05-04 | Rca Corporation | Diphenyl continuous foam dyeing with fabric running over rolls in foam bath |
AR205639A1 (en) * | 1974-04-03 | 1976-05-21 | Hoechst Ag | PROCEDURE FOR OBTAINING STAINS AND STAMPINGS ON FIBROUS CELLULOSIC MATERIALS |
US3932129A (en) * | 1974-07-17 | 1976-01-13 | Rick Anthony Porter | Space dyed yarn production using dense foams |
CH590961B5 (en) * | 1975-05-28 | 1977-08-31 | Hoechst Ag | |
BE853697A (en) * | 1975-06-06 | 1977-08-16 | United Merchants & Mfg | FABRIC TREATMENT PROCESS |
US4099913A (en) * | 1976-03-25 | 1978-07-11 | Union Carbide Corporation | Foams for treating fabrics |
DE2722083B2 (en) * | 1977-05-16 | 1980-10-02 | Union Carbide Corp., New York, N.Y. (V.St.A.) | Process for the continuous treatment of a porous fabric, textile or paper substrate by applying foamed agents |
-
1979
- 1979-09-18 WO PCT/US1979/000759 patent/WO1980000545A1/en unknown
- 1979-09-18 GB GB8015024A patent/GB2051885B/en not_active Expired
- 1979-09-18 JP JP50164279A patent/JPS55500762A/ja active Pending
- 1979-09-18 CA CA335,904A patent/CA1132762A/en not_active Expired
- 1979-09-19 AU AU50970/79A patent/AU525522B2/en not_active Ceased
- 1979-09-19 EP EP19790103530 patent/EP0009721B1/en not_active Expired
- 1979-09-19 BR BR7905992A patent/BR7905992A/en unknown
-
1980
- 1980-05-19 SE SE8003726A patent/SE8003726L/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
SE8003726L (en) | 1980-05-19 |
AU525522B2 (en) | 1982-11-11 |
GB2051885B (en) | 1982-10-20 |
GB2051885A (en) | 1981-01-21 |
EP0009721A1 (en) | 1980-04-16 |
WO1980000545A1 (en) | 1980-04-03 |
AU5097079A (en) | 1980-03-27 |
CA1132762A (en) | 1982-10-05 |
BR7905992A (en) | 1980-06-03 |
JPS55500762A (en) | 1980-10-09 |
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