US3103404A - Discharge printing - Google Patents
Discharge printing Download PDFInfo
- Publication number
- US3103404A US3103404A US3103404DA US3103404A US 3103404 A US3103404 A US 3103404A US 3103404D A US3103404D A US 3103404DA US 3103404 A US3103404 A US 3103404A
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- US
- United States
- Prior art keywords
- discharge
- parts
- cellulose
- textile material
- water
- 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 - Lifetime
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- 238000010018 discharge printing Methods 0.000 title claims description 28
- 239000004753 textile Substances 0.000 claims description 66
- 239000000463 material Substances 0.000 claims description 64
- 239000000203 mixture Substances 0.000 claims description 52
- 239000003795 chemical substances by application Substances 0.000 claims description 46
- -1 HYDROXYL GROUPS Chemical group 0.000 claims description 40
- 229920002678 cellulose Polymers 0.000 claims description 40
- 239000001913 cellulose Substances 0.000 claims description 40
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 38
- 238000010025 steaming Methods 0.000 claims description 32
- 239000002562 thickening agent Substances 0.000 claims description 28
- 238000000034 method Methods 0.000 claims description 22
- 238000001035 drying Methods 0.000 claims description 14
- 239000002253 acid Substances 0.000 claims description 8
- 150000007524 organic acids Chemical class 0.000 claims 2
- 238000004326 stimulated echo acquisition mode for imaging Methods 0.000 claims 2
- 239000004744 fabric Substances 0.000 description 26
- 230000002522 swelling Effects 0.000 description 26
- 229910052751 metal Inorganic materials 0.000 description 22
- 239000002184 metal Substances 0.000 description 22
- 229920002301 Cellulose acetate Polymers 0.000 description 20
- 239000000975 dye Substances 0.000 description 20
- 239000000835 fiber Substances 0.000 description 20
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 20
- 230000000694 effects Effects 0.000 description 18
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 16
- YODZTKMDCQEPHD-UHFFFAOYSA-N Thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 14
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 14
- 238000010438 heat treatment Methods 0.000 description 14
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- 229940017705 formaldehyde sulfoxylate Drugs 0.000 description 12
- SBGKURINHGJRFN-UHFFFAOYSA-N hydroxymethanesulfinic acid Chemical compound OCS(O)=O SBGKURINHGJRFN-UHFFFAOYSA-N 0.000 description 12
- 230000002441 reversible Effects 0.000 description 12
- 229920000161 Locust bean gum Polymers 0.000 description 10
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 10
- 239000003906 humectant Substances 0.000 description 10
- 238000010409 ironing Methods 0.000 description 10
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 10
- 239000004310 lactic acid Substances 0.000 description 10
- 235000014655 lactic acid Nutrition 0.000 description 10
- 239000000711 locust bean gum Substances 0.000 description 10
- 235000010420 locust bean gum Nutrition 0.000 description 10
- 239000000126 substance Substances 0.000 description 10
- 125000001931 aliphatic group Chemical group 0.000 description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 8
- 239000004408 titanium dioxide Substances 0.000 description 8
- WDHSSYCZNMQRNF-UHFFFAOYSA-L CTK1A4617 Chemical compound [Zn+2].O=C.[O-]S[O-] WDHSSYCZNMQRNF-UHFFFAOYSA-L 0.000 description 6
- XWGJFPHUCFXLBL-UHFFFAOYSA-M Rongalite Chemical compound [Na+].OCS([O-])=O XWGJFPHUCFXLBL-UHFFFAOYSA-M 0.000 description 6
- 150000001298 alcohols Chemical class 0.000 description 6
- 238000007599 discharging Methods 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- 150000002170 ethers Chemical class 0.000 description 6
- QJQZEJFUIOWFMS-UHFFFAOYSA-N formaldehyde;sulfanediol Chemical class O=C.OSO QJQZEJFUIOWFMS-UHFFFAOYSA-N 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 238000007639 printing Methods 0.000 description 6
- 239000000344 soap Substances 0.000 description 6
- HCHKCACWOHOZIP-UHFFFAOYSA-N zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 6
- 229910052725 zinc Inorganic materials 0.000 description 6
- 239000011701 zinc Substances 0.000 description 6
- WAPNOHKVXSQRPX-UHFFFAOYSA-N 1-phenylethanol Chemical compound CC(O)C1=CC=CC=C1 WAPNOHKVXSQRPX-UHFFFAOYSA-N 0.000 description 4
- MTHSVFCYNBDYFN-UHFFFAOYSA-N Diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 4
- OKMQHKAXPFUWKR-UHFFFAOYSA-L S([O-])[O-].C=O.[Ba+2] Chemical class S([O-])[O-].C=O.[Ba+2] OKMQHKAXPFUWKR-UHFFFAOYSA-L 0.000 description 4
- 210000003491 Skin Anatomy 0.000 description 4
- 229920002472 Starch Polymers 0.000 description 4
- FERIUCNNQQJTOY-UHFFFAOYSA-M butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000002845 discoloration Methods 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 235000021317 phosphate Nutrition 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 239000004627 regenerated cellulose Substances 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 235000019698 starch Nutrition 0.000 description 4
- 239000008107 starch Substances 0.000 description 4
- FMWCKLXINCGQFM-UHFFFAOYSA-N 1-methoxyethyl acetate Chemical compound COC(C)OC(C)=O FMWCKLXINCGQFM-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N AI2O3 Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 2
- PZZYQPZGQPZBDN-UHFFFAOYSA-N Aluminium silicate Chemical compound O=[Al]O[Si](=O)O[Al]=O PZZYQPZGQPZBDN-UHFFFAOYSA-N 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 2
- FYGDTMLNYKFZSV-MRCIVHHJSA-N Dextrin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)OC1O[C@@H]1[C@@H](CO)OC(O[C@@H]2[C@H](O[C@H](O)[C@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O FYGDTMLNYKFZSV-MRCIVHHJSA-N 0.000 description 2
- 229920002456 HOTAIR Polymers 0.000 description 2
- FEWJPZIEWOKRBE-XIXRPRMCSA-N Mesotartaric acid Chemical compound OC(=O)[C@@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-XIXRPRMCSA-N 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- GCLGEJMYGQKIIW-UHFFFAOYSA-H Sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 2
- DQWPFSLDHJDLRL-UHFFFAOYSA-N Triethyl phosphate Chemical compound CCOP(=O)(OCC)OCC DQWPFSLDHJDLRL-UHFFFAOYSA-N 0.000 description 2
- HWKQNAWCHQMZHK-UHFFFAOYSA-N Trolnitrate Chemical compound [O-][N+](=O)OCCN(CCO[N+]([O-])=O)CCO[N+]([O-])=O HWKQNAWCHQMZHK-UHFFFAOYSA-N 0.000 description 2
- DQEFEBPAPFSJLV-WLTGXWPBSA-N [(2R,3R,4S,5R,6S)-4,5,6-tri(propanoyloxy)-3-[(2S,3R,4S,5R,6R)-3,4,5-tri(propanoyloxy)-6-(propanoyloxymethyl)oxan-2-yl]oxyoxan-2-yl]methyl propanoate Chemical compound CCC(=O)OC[C@H]1O[C@@H](OC(=O)CC)[C@H](OC(=O)CC)[C@@H](OC(=O)CC)[C@@H]1O[C@H]1[C@H](OC(=O)CC)[C@@H](OC(=O)CC)[C@H](OC(=O)CC)[C@@H](COC(=O)CC)O1 DQEFEBPAPFSJLV-WLTGXWPBSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive Effects 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 239000000987 azo dye Substances 0.000 description 2
- 239000000440 bentonite Substances 0.000 description 2
- 229910000278 bentonite Inorganic materials 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 235000014633 carbohydrates Nutrition 0.000 description 2
- 150000001720 carbohydrates Chemical class 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000001808 coupling Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- QGKLCGVVGGFZBS-UHFFFAOYSA-N formaldehyde;zinc Chemical compound [Zn].O=C QGKLCGVVGGFZBS-UHFFFAOYSA-N 0.000 description 2
- 229910000286 fullers earth Inorganic materials 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- 229920000591 gum Polymers 0.000 description 2
- 230000002209 hydrophobic Effects 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 230000005012 migration Effects 0.000 description 2
- 230000001264 neutralization Effects 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N oxane Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- 230000001590 oxidative Effects 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 230000002035 prolonged Effects 0.000 description 2
- 239000002964 rayon Substances 0.000 description 2
- 238000009991 scouring Methods 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000600 sorbitol Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 229960001367 tartaric acid Drugs 0.000 description 2
- 239000011975 tartaric acid Substances 0.000 description 2
- 235000002906 tartaric acid Nutrition 0.000 description 2
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 2
- RXPQRKFMDQNODS-UHFFFAOYSA-N tripropyl phosphate Chemical compound CCCOP(=O)(OCCC)OCCC RXPQRKFMDQNODS-UHFFFAOYSA-N 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- 238000004383 yellowing Methods 0.000 description 2
Classifications
-
- 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
- D06P5/15—Locally discharging the dyes
- D06P5/155—Locally discharging the dyes with reductants
-
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/92—Synthetic fiber dyeing
- Y10S8/921—Cellulose ester or ether
Definitions
- the activecomponents of the discharge composition are able to penetrate into the fibers while of course not injuring the fibers themselves.
- the substances left in the fibers after discharge has been effected must also be capable of being taken curt of the fibers.
- the discharge composition of course must not be too fiuid lest it migrate from the selected areas where applied and act on areas not intended to be discharged.
- selected areas of textile materials of [organic acid esters of cellulose of low free hy'droxyl content, and containing dye or dye components are treated with an aqueous composition containing a metal formaldehyde sulfoxylate, a reversible hydrophilic thickener, and a swelling agent selected from the group consisting of phenyl-methylcarbinol, tri-lower alkyl phosphates such as triethyl phosphate and ethers and/ or esters of aliphatic polyhydroxy compounds, e.g., of glycols, such as B-phenoxyethanol, glycol diacetate, methoxyethyl acetate.
- the texmile printed with the discharge composition is dried, steamed and thereafterv scoured.
- thetextile is heat treated to improve its glaze resistance and to increase its crystallinity and safe ironing temperature in the event that it has not been heat treated either before .or during the discharge printing.
- a metal formaldehyde sulfioxylate there are present from about 15- to parts by weight of a metal formaldehyde sulfioxylate and preferably 20* to 30 parts by weight. While monovalent metal formaldehyde sulfoxylates such as sodium formaldehyde sulfoxylate can be used, the formaldehyde sulfoxylates of polyvalent metals are preferred because reduction of the dischargeable dyes is best effected on the neutral or slightly acid side and sodium formaldehyde sulfoxylate, for example, is not stable on the slightly acid side.
- Representative polyvalent metal formaldehyde sulfoxylates include zinc and barium formaldehyde sulfoxylates and best results are achieved with zinc formaldehyde sulfoxylate.
- the swelling agent serves to swell the fibers and to permit the metal formaldehyde sulfoxylate to attack the dyestuff within the fibers. Its swelling action, however, must not be so great as to cause the fibers to coalesce or otherwise'to be damaged. Satisfactory results are achieved using from about 2 to 10 or preferably 2 to 6 parts by weight of one I01 a mixture of swelling agents.
- the preferred swelling agent is B-phenoxyethanol.
- oxyethylated locust bean gum prepared by reacting locust beam gun with ethylene oxide is preferred because it does not break down even at the temperatures of pressurized steam and because of the quality of the discharge, its sharpness and freedom from discoloration.
- a watermiscible aliphatic polyhydroxy compound is included in the discharge composition as a humectant.
- the humectaut brings the water within the fiber where it is necessary for the metal formaldehyde sulfoxylate to reduce the dye.
- Representative water-miscible aliphatic polyhydroxy oom pounds include glycerol, sorbitol, ethylene glycol, diethylene glycol and higher polyethylene glycols, and preferably thiodiethylene glycol.
- a water-soluble hydroxylated lower aliphatic acid such as tartaric acid and preferably citric or lactic acid increase .the discharge effect and are especially useful where a white rather than an illuminated discharge is desired.
- an inorganic, insoluble water binding additive may be incorporated into the discharge composition to prevent spreading of the discharge agent upon steaming, thereby improving the sharpness of the discharge prints.
- Suitable substances include the oxides of one or more metals and/ or silicon, such as bentonite, kaolin, fullers earth, silica, alumina, and especially titanium dioxide.
- a dye or pigment may be incor- For each 40 to parts by weight of water in the disporated' into the discharge compositions so that the discharge printed areas Will take on a newcolor different from their original color.
- composition is prepared by first mixing the thick ener and water followed'by stirring in the Water-solubles,
- the discharge compositions or pastes are applied in conventional manner such as with a screen to colored textile materials made up in whole or in part of organic acid esters of cellulose of low free hydroxyl content, i.e. less than about 0.29 free hydroxyl groups per anhydroglucose unit of the cellulose molecule.
- Representative esters include cellulose propionate, cellulose 'butyrate, cellulose acetate'butyrate, and the like, although cellulose acetate is preferred.
- cellulose acetate having 0.29 free hydroxyl groups per anhydroglucose unit i.e. an acetyl value of at least about 59% by weight calculated as combined acetic acid, is suitable, preferably the acetyl value is at least 61%.
- a particularly suitable fiber is composed of a core of a cellulose acetate of a high acetyl value having an integral thin skin of regenerated cellulose such as is produced by a surface saponiiication of cellulose acetate having an acetyl value of at least 59%.
- Such highly est'eriiied cellulose is capable of developing relatively high crystallinity and of being ironed safely at temperatures in excess of 200 C. upon suitable heat treatment.
- the textile material which is printed with the discharge paste contains organic acid esters of cellulose Which have not been treated since heat treated materials are considerably more diilicult to discharge.
- the textile material printed with the discharge compositi-on is dried in air and/ or an oven and thereafter steamed to effect discharge, followed by scouring.
- the steaming generally lasts at least minutes to effect adequate discharge.
- steaming is effected at atmospheric pressure with steam at a temperature of about 216 F., it is generally desirable to effect a heat treat ment to improve the physical properties of the textile material.
- the textile material is dried and is then heat treated with hot air or the like in the manner described in the copending application of Salvin et al., Ser. No. 472,758, filed December 2, 1954, now US. Patent No. 2,982,597.
- the steaming is effected at a temperature in excess of about 237 F. and preferably from about 239 to 250 F., the steam being under sufficient pressure to permit such temperatures, e.g. about 9 p.s.ig. or more.
- the pressure steaming may last from about 45 to 75 minutes, the exact duration depending upon the temperature; at the lower temperatures one hour steaming is adequate.
- the pressure steaming produces a sharp discharge and also effects heat treatment so that no separate treatment for this purpose is necessary. Heat treatment following normal steaming sometimes yellows the discharge areas slightly, but this yellowing is not evidenced when the steaming is carried out under such conditions as will simultaneously effect heat treatment.
- the term colored in describing the starting textile material has reference to dinectly vis ible color as well as to potentially visible color as when one component of an azo dye is in the fiber and visible color will later be developed by coupling on thefiber.
- the color whether apparent or latent, i.e. Whether the starting material is impregnated with a dyestuff or a component thereof, must of course be one which is capethanol, 20 parts of zinc able of being discharged; the classes of substances which :are discharge/able are well-known.
- Example I 11855) in the prmence of tripropyl phosphate is printed with a discharge paste comprising by weight 4.2 parts of oxyethylat-ed locust bean gum, 8 parts of ,H-phenoxyformaldehyde sulfoxylate, 2 parts of lactic acid, 2 parts of thiodiethylene glycol, 10 parts of titanium dioxide and 80.8 parts of water.
- the fabric is dried in air for 30 minutes and then in an oven at 140 F; forS minutes.
- Example 11 Example III The process of Exmple 1(a) and (b) is repeated substituting citric acid for lactic acid. A slightly better discharging eifeot is realized. lf theacid is omitted altogether the discharge effect is not quite as complete.
- Example 1(a) and (b) The process of Example 1(a) and (b) is repeated, varying the proportions of ,B-phenoxyethanol and thiodiethylene glycol. Best results are achieved when 4 to 6 parts of each are present.
- the blue fabric is printed with a colored discharge composition comprising 5 parts of 'oxyethylated locust bean gum, 83 parts of water, 20 parts of zinc formaldehyde sulfoxylate, 2 parts of thiodiethylene glycol, 10 parts of glycol diacetate and 10 parts of Cibanone Brilliant Green BF (Color Index No. 1101).
- the fabric After printing the fabric is dried for 10 minutes at 140 F., is steamed for 1 hour with saturated steam at 239 F. and 10 p.s.i.g., scoured for 20 minutes at F. in water containing 1 gram per liter of soap, and then dried for 10 minutes at 140 F.
- the printed areas are bright green on a blue background.
- the lines of demarcation are sharp and the fabric is level, resistant to crocking and resistant to color change in an oxidizing bath.
- the safe ironing temperature of the fabric is 450 F. as compared with a safe ironing temperature of 374 F. for the fabric prior to printing with the discharge composition.
- a discharge printing composition comprising by weight about 40 to 80 parts of water, about 15 to 30 parts of a discharge agent, about 2 to 10 parts of a swelling agent for the organic acid ester of cellulose, about 1 to 7 parts of a thickener and about 2 to 6 parts of a humectant, drying the textile material and steaming the textile material with steam at a temperature in excess of about 237 F. and a pressure in excess of about 9 p.s.i.g.
- a discharge printing composition comprising by weight about 40 to 80 parts of water, about 20 to 30 parts of zinc formaldehyde sulfoxylate as discharge agent, about 2 to 10 parts of fl-phenoxyethanol as swelling agent for the cellulose acetate, about 1 to 7 parts of oxyethylated locust bean gum as thickener, about 2 to 6 parts of thiodiethylene glycol as humectant, about 2 to 4 parts of lactic acid and about 5 to 10 parts of titanium dioxide.
- a discharge printing composition comprising by weight about 40 to 80 parts of water, about '15 mo 30 parts of a polyvalent metal formaldehyde sulfoxylate as discharge agent, about 2 to 10 parts of a swelling agent for the organic acid ester of cellulose and about 1 to 7 parts of a reversible hydrophilic thickener, drying the textile material and then steaming the textile material until the printed areas are discharged, said swelling agent comprising at least one member selected from the group consisting of phenyl-methyl carbinol, tri-lower alkyl phosphates, ethers of polyhydric alcohols, esters of polyhydric alcohols and ether-esters of polyhydric alcohols.
- the process which comprises applying to selected areas of a colored textile material comprising an organic acid ester of cellulose having less than about 0.29 free hydroxyl groups per anhydroglucose unit a discharge printing composition comprising by weight about 40' to 80 parts of water, about 15 to 30 parts of a polyvalent metal formaldehyde sulfoxylate as discharge agent, about 2 to 10 parts of a swelling agent for the organic acid ester of cellulose comprising fi-phenoxyethan-ol and about 1 to 7 parts of a reversible hydrophilic thickener, drying the textile material and then steaming the textile material until the printed areas are discharged.
- a discharge printing composition comprising by weight about 40 to 80 parts of water, about 15 to 30 parts of a discharge agent selected from the group consisting of zinc and barium formaldehyde sulfoxylate, about 2 to 10 parts of a swelling agent comprising B-phenoxyethanol, about 1 to 7 parts of a reversible hydrophilic thickener and about 2 to 6 parts by weight of a water-rniscible humectant comprising thiodiethylene glycol.
- a discharge agent selected from the group consisting of zinc and barium formaldehyde sulfoxylate
- a swelling agent comprising B-phenoxyethanol
- a reversible hydrophilic thickener about 2 to 6 parts by weight of a water-rniscible humectant comprising thiodiethylene glycol.
Description
United States Patent ground while in colored or illuminated discharge printing the selected areas lose their original color and are dyed a different color 'by a dye incorporated in the discharge composition. The discharging reaction must take place where the dye to be discharged, i.e. destroyed, is located.
It is therefore necessary that the activecomponents of the discharge composition are able to penetrate into the fibers while of course not injuring the fibers themselves. The substances left in the fibers after discharge has been effected must also be capable of being taken curt of the fibers. The discharge composition of course must not be too fiuid lest it migrate from the selected areas where applied and act on areas not intended to be discharged.
While it would be desirable to discharge print textile materials comprising organic acid esters of cellulose of low free hydroxyl content, conventional discharge pastes and processes are not satisfactory as applied to such materials in that the treated areas are fuzzy and not distinctly set' off from the untreated areas and in that not all of the color is discharged even in the treated areas and discharge products are not removed, resulting in discoloration on exposure to light, heat and gas.
It is accordingly an object of the present invention to provide discharge compositions suited for discharge printing of textile materials comprising organic acid esters of cellulose of low free hydroxyl content.
It is a further object of the invention to provide a novel procedure for the discharge printing of colored textile materials comprising organic acid esters of cellulose of low free hydroxyl content.
It is a further object of the invention to provide a novel procedure fior simultaneously discharging the color from selected areas of colored textile materials. of organic acid esters of cellulose of low free hydroxyl content, and for improving the physical properties of the textile material.
Other objects and advantages will be apparent from the following description and claims. Throughout the following description and claims all parts and percentages refer to weight units unless otherwise specified. In accordance with one aspect of the present invention, selected areas of textile materials of [organic acid esters of cellulose of low free hy'droxyl content, and containing dye or dye components, are treated with an aqueous composition containing a metal formaldehyde sulfoxylate, a reversible hydrophilic thickener, and a swelling agent selected from the group consisting of phenyl-methylcarbinol, tri-lower alkyl phosphates such as triethyl phosphate and ethers and/ or esters of aliphatic polyhydroxy compounds, e.g., of glycols, such as B-phenoxyethanol, glycol diacetate, methoxyethyl acetate.
The texmile printed with the discharge composition is dried, steamed and thereafterv scoured. Advantageously thetextile is heat treated to improve its glaze resistance and to increase its crystallinity and safe ironing temperature in the event that it has not been heat treated either before .or during the discharge printing.
2 charge composition there are present from about 15- to parts by weight of a metal formaldehyde sulfioxylate and preferably 20* to 30 parts by weight. While monovalent metal formaldehyde sulfoxylates such as sodium formaldehyde sulfoxylate can be used, the formaldehyde sulfoxylates of polyvalent metals are preferred because reduction of the dischargeable dyes is best effected on the neutral or slightly acid side and sodium formaldehyde sulfoxylate, for example, is not stable on the slightly acid side. Representative polyvalent metal formaldehyde sulfoxylates include zinc and barium formaldehyde sulfoxylates and best results are achieved with zinc formaldehyde sulfoxylate. I
The swelling agent serves to swell the fibers and to permit the metal formaldehyde sulfoxylate to attack the dyestuff within the fibers. Its swelling action, however, must not be so great as to cause the fibers to coalesce or otherwise'to be damaged. Satisfactory results are achieved using from about 2 to 10 or preferably 2 to 6 parts by weight of one I01 a mixture of swelling agents. The preferred swelling agent is B-phenoxyethanol.
About l to 7 and preferably 2 to 5 parts by weight of the reversible hydrophilic thickener should be present in the discharge composition; it serves to thicken the composition and thus to prevent migration of the components 7 beyond the areas to which the composition is selectively applied. In addition to its thickening properties, the thickener should not break down even at temperatures in excess of the boiling point of water at atmospheric pressure and must be hydrophilically reversible, ie it must be capable of re-wetting even after hard drying to permit the thickener to be washed out following discharge. The thickener, of course, must be compatible with the metal formaldehyde sulfoxylate. While vegetable carbohydrate gums such as 3.1310 gum, British gum, and starch ethers. such as methylated and carboxylated starch are suitable, oxyethylated locust bean gum (prepared by reacting locust beam gun with ethylene oxide) is preferred because it does not break down even at the temperatures of pressurized steam and because of the quality of the discharge, its sharpness and freedom from discoloration.
Especially good results are achieved when from about 2 to 8 and preferably 2 to 6 parts by weight of a watermiscible aliphatic polyhydroxy compound is included in the discharge composition as a humectant. The humectaut brings the water within the fiber where it is necessary for the metal formaldehyde sulfoxylate to reduce the dye. Representative water-miscible aliphatic polyhydroxy oom pounds include glycerol, sorbitol, ethylene glycol, diethylene glycol and higher polyethylene glycols, and preferably thiodiethylene glycol.
About 1 to 6 and preferably 2 to 4 parts by weight of a water-soluble hydroxylated lower aliphatic acid such as tartaric acid and preferably citric or lactic acid increase .the discharge effect and are especially useful where a white rather than an illuminated discharge is desired.
Up to about 15 and preferably 5 to 10 parts by weight of an inorganic, insoluble water binding additive may be incorporated into the discharge composition to prevent spreading of the discharge agent upon steaming, thereby improving the sharpness of the discharge prints. Suitable substances include the oxides of one or more metals and/ or silicon, such as bentonite, kaolin, fullers earth, silica, alumina, and especially titanium dioxide.
If desired, up to about 2'0 and preferably from 1 to 15 parts .by weight of a dye or pigment may be incor- For each 40 to parts by weight of water in the disporated' into the discharge compositions so that the discharge printed areas Will take on a newcolor different from their original color.
The composition is prepared by first mixing the thick ener and water followed'by stirring in the Water-solubles,
the discharge agent and then the hydrophobic ingredients. Solid substances are added either as solutions or dispersions in Water.
The discharge compositions or pastes are applied in conventional manner such as with a screen to colored textile materials made up in whole or in part of organic acid esters of cellulose of low free hydroxyl content, i.e. less than about 0.29 free hydroxyl groups per anhydroglucose unit of the cellulose molecule. Representative esters include cellulose propionate, cellulose 'butyrate, cellulose acetate'butyrate, and the like, although cellulose acetate is preferred. While cellulose acetate having 0.29 free hydroxyl groups per anhydroglucose unit, i.e. an acetyl value of at least about 59% by weight calculated as combined acetic acid, is suitable, preferably the acetyl value is at least 61%. A particularly suitable fiber is composed of a core of a cellulose acetate of a high acetyl value having an integral thin skin of regenerated cellulose such as is produced by a surface saponiiication of cellulose acetate having an acetyl value of at least 59%.
Such highly est'eriiied cellulose is capable of developing relatively high crystallinity and of being ironed safely at temperatures in excess of 200 C. upon suitable heat treatment. Preferably, however, the textile material which is printed with the discharge paste contains organic acid esters of cellulose Which have not been treated since heat treated materials are considerably more diilicult to discharge.
The textile material printed with the discharge compositi-on is dried in air and/ or an oven and thereafter steamed to effect discharge, followed by scouring. The steaming generally lasts at least minutes to effect adequate discharge. When steaming is effected at atmospheric pressure with steam at a temperature of about 216 F., it is generally desirable to effect a heat treat ment to improve the physical properties of the textile material. To this :end, following steaming the textile material is dried and is then heat treated with hot air or the like in the manner described in the copending application of Salvin et al., Ser. No. 472,758, filed December 2, 1954, now US. Patent No. 2,982,597.
In a preferred embodiment of the invention, the steaming is effected at a temperature in excess of about 237 F. and preferably from about 239 to 250 F., the steam being under sufficient pressure to permit such temperatures, e.g. about 9 p.s.ig. or more. The pressure steaming may last from about 45 to 75 minutes, the exact duration depending upon the temperature; at the lower temperatures one hour steaming is adequate. The pressure steaming produces a sharp discharge and also effects heat treatment so that no separate treatment for this purpose is necessary. Heat treatment following normal steaming sometimes yellows the discharge areas slightly, but this yellowing is not evidenced when the steaming is carried out under such conditions as will simultaneously effect heat treatment.
As employed herein, the term colored in describing the starting textile material has reference to dinectly vis ible color as well as to potentially visible color as when one component of an azo dye is in the fiber and visible color will later be developed by coupling on thefiber. The color whether apparent or latent, i.e. Whether the starting material is impregnated with a dyestuff or a component thereof, must of course be one which is capethanol, 20 parts of zinc able of being discharged; the classes of substances which :are discharge/able are well-known.
The following examples are given to illustrate this invention further.
Example I 11855) in the prmence of tripropyl phosphate, is printed with a discharge paste comprising by weight 4.2 parts of oxyethylat-ed locust bean gum, 8 parts of ,H-phenoxyformaldehyde sulfoxylate, 2 parts of lactic acid, 2 parts of thiodiethylene glycol, 10 parts of titanium dioxide and 80.8 parts of water. The fabric is dried in air for 30 minutes and then in an oven at 140 F; forS minutes.
(b) A portion of the dried fabric from (2) is steamed for 10 minutes with steam at atmospheric pressure and 216 F., scoured for 15 minutes at F. in water containing 1 gram per liter of soap and 1 gram per liter of sodium hexarnetaphosphate, and then dried in an oven at F. There is obtained a full dischargeeifect with a good sharp edge. The fabric is then heat treated in air for 30 seconds at 446 F. and its safe ironing temperature ,-is raised from 374 F. to 450 F. The discharge area yellows slightly as a result of the heat treatment. If the fabric is heat treated prior to discharge printing, the discharge effect and the sharpness of the edge are not as good as when discharge is effected before heat treatment, but the sharpness of the mark is better.
(c) Another portion of the dried fabric from (a) is steamed for 1 hour with steam at 10 p.s.iig. and 239 F. The fabric is secured for 15 minutes at F. in Water containing 1 gram per liter of soap and 1 gram per liter of sodium hexametaphosphate, is dried in air for 30 minutes and is then dried for 10 minutes in an oven at 140 F. The discharge effect and sharpness are as good as in (b), the discharge area is White and does not discolor even upon prolonged exposure, and the safe ironing emperature of the fabric is 450 F.
Example 11 Example III The process of Exmple 1(a) and (b) is repeated substituting citric acid for lactic acid. A slightly better discharging eifeot is realized. lf theacid is omitted altogether the discharge effect is not quite as complete.
Example IV,
The process of Example 1(a) and (b) is repeated, varying the proportions of ,B-phenoxyethanol and thiodiethylene glycol. Best results are achieved when 4 to 6 parts of each are present.
Example A fabric woven of a cellulose acetate yarn having an average acetyl value of 59.5% and composed of filaments having a thin skin of regenerated cellulose integral with a core of cellulose acetate having an acetyl value of 61%, is dyed blue in conventional manner with Eastone Blue GFD to pick up 3% by weight of the dye. The blue fabric is printed with a colored discharge composition comprising 5 parts of 'oxyethylated locust bean gum, 83 parts of water, 20 parts of zinc formaldehyde sulfoxylate, 2 parts of thiodiethylene glycol, 10 parts of glycol diacetate and 10 parts of Cibanone Brilliant Green BF (Color Index No. 1101). After printing the fabric is dried for 10 minutes at 140 F., is steamed for 1 hour with saturated steam at 239 F. and 10 p.s.i.g., scoured for 20 minutes at F. in water containing 1 gram per liter of soap, and then dried for 10 minutes at 140 F. The printed areas are bright green on a blue background. The lines of demarcation are sharp and the fabric is level, resistant to crocking and resistant to color change in an oxidizing bath. The safe ironing temperature of the fabric is 450 F. as compared with a safe ironing temperature of 374 F. for the fabric prior to printing with the discharge composition.
It is to be understood that the foregoing detailed description is given merely by Way of illustration and that many variations may be made therein without departing from the spirit of our invention.
Having described our invention, what we desire to secure by Letters Patent is:
1. The process which comprises applying to selected areas of a colored textile material comprising an organic acid ester of cellulose having less than about 0.29 free hydroxyl groups per anhydnoglucose unit a discharge printing composition comprising water, a discharge agent, a swelling agent for the organic acid ester of cellulose and a thickener, drying the textile material, and steaming the textile material with steam at a temperature in excess of about 237 F. and a pressure in excess of about 9 p.s.i.g.
2. The process which comprises applying to selected areas of a colored textile material comprising an organic acid ester of cellulose having less than about 0.29 free hydroxyl groups per anhydroglucose unit a discharge printing composition comprising by weight about 40 to 80 parts of water, about 15 to 30 parts of a discharge agent, about 2 to 10 parts of a swelling agent for the organic acid ester of cellulose, about 1 to 7 parts of a thickener and about 2 to 6 parts of a humectant, drying the textile material and steaming the textile material with steam at a temperature in excess of about 237 F. and a pressure in excess of about 9 p.s.i.g.
3. The process which comprises applying to selected areas of a colored textile material comprising cellulose acetate having an acetyl value of at least about 61% by weight calculated as combined acetic acid a discharge printing composition comprising by weight about 40 to 80 parts of water, about 20 to 30 parts of zinc formaldehyde sulfoxylatte as discharge agent, about 2 to 10 parts of B-phenoxyethanol as swelling agent for the cellulose acetate, about 1 to 7 parts of oxyethylated locust bean gum as thickener, about 2 to 6 parts of thiodiethylene glycol as humectant, about 2 to 4 parts of lactic acid and about to parts of titanium dioxide, drying the textile material, and steaming the textile material with steam at a temperature in excess of about 237 F. and a pressure in excess of about 9 p.s.i.g.
4. A discharge printing composition comprising by weight about 40 to 80 parts of water, about 20 to 30 parts of zinc formaldehyde sulfoxylate as discharge agent, about 2 to 10 parts of fl-phenoxyethanol as swelling agent for the cellulose acetate, about 1 to 7 parts of oxyethylated locust bean gum as thickener, about 2 to 6 parts of thiodiethylene glycol as humectant, about 2 to 4 parts of lactic acid and about 5 to 10 parts of titanium dioxide.
5. The process which comprises applying to selected areas of a colored textile material comprising an organic acid ester of cellulose having less than about 0.29 free hydnoxyl groups per anhydroglucose unit a discharge printing composition comprising by weight about 40 to 80 parts of water, about '15 mo 30 parts of a polyvalent metal formaldehyde sulfoxylate as discharge agent, about 2 to 10 parts of a swelling agent for the organic acid ester of cellulose and about 1 to 7 parts of a reversible hydrophilic thickener, drying the textile material and then steaming the textile material until the printed areas are discharged, said swelling agent comprising at least one member selected from the group consisting of phenyl-methyl carbinol, tri-lower alkyl phosphates, ethers of polyhydric alcohols, esters of polyhydric alcohols and ether-esters of polyhydric alcohols.
6. The process which comprises applying to selected areas of a colored textile material comprising an organic acid ester of cellulose having less than about 0.29 free hydroxyl groups per anhydroglucose unit a discharge printing composition comprising by weight about 40' to 80 parts of water, about 15 to 30 parts of a polyvalent metal formaldehyde sulfoxylate as discharge agent, about 2 to 10 parts of a swelling agent for the organic acid ester of cellulose comprising fi-phenoxyethan-ol and about 1 to 7 parts of a reversible hydrophilic thickener, drying the textile material and then steaming the textile material until the printed areas are discharged.
7. A discharge printing composition comprising by weight about 40 to 80 parts of water, about 15 to 30 parts of a discharge agent selected from the group consisting of zinc and barium formaldehyde sulfoxylate, about 2 to 10 parts of a swelling agent comprising B-phenoxyethanol, about 1 to 7 parts of a reversible hydrophilic thickener and about 2 to 6 parts by weight of a water-rniscible humectant comprising thiodiethylene glycol.
References Cited in the file of this patent UNITED STATES PATENTS 1,864,582 Bynod June 28, 1932 2,109,709 Pfister Mar. 1, 1938 2,248,128 Seymour July 8, 1941 2,409,980 Jensen Oct. 22, 1946 2,435,658 Seymour Feb. 10, 1948 2,862,785 Finlayson Dec. 2, 1958 2,874,022 Raff Feb. 17, 1959 FOREIGN PATENTS 342,333 Great Britain Jan. 26, 1931 OTHER REFERENCES Shaw: I.S.D.C., vol. 67, pp. 599-608, December 1951. Knecht and Fothergill: The Principles and Practice of Textile Printing, 4th Ed., 1952, p. 667.
Fortess: Amer. Dyest. 537.
British Rayon and Silk Journal, April 1955, pp. 72, 74.
Mellor: J.S.D.C., vol. 71, No. 13, December 1955, pp. 817-829.
Fortess: Amer. Dyest. Rep., February 13, 1956, pp. 88-94.
Man-Made Textiles, February 1956, pp. 54-55; March 1957, pp. 72-73; September 1957, pp. 61-62.
Speel: Textile Chemicals and Auxiliaries, 1957, pp. 270 and 296.
Rep, August 1, 1955, pp. 524-
Claims (1)
1. THE PROCESS WHICH COMPRISES APPLYING TO SEELCTED AREAS OF A COLORED TEXTILE MATERIAL COMPRISING AN ORHANIC ACID ESTER OF CELLULOSE HAVING LESS THAN ABOUT 0.29 FREE HYDROXYL GROUPS PER ANHYDROGLUCOSE UNIT A DISCHARGE PRINTING COMPOSITION COMPRISING WATER, A DISCHARGE AGENT, ASWELLING AGENT FOR THE ORGANIC ACID ESTER OF CELLULOSE AND A THICKENER, DRYING THE TEXTILE MATERIAL, AND STEAMING THE TEXTILE MATERIAL WITH STEAM AT A TEMPERATURE IN EXCESS OF ABOUT 237*F. AND A PRESSURE IN EXCESS OF ABOUT 9 P.S.I.G.
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US3103404A true US3103404A (en) | 1963-09-10 |
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US3103404D Expired - Lifetime US3103404A (en) | Discharge printing |
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Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3923457A (en) * | 1972-10-12 | 1975-12-02 | Hoechst Ag | Mixtures of fixing auxiliaries containing novel dye carrier |
US3972677A (en) * | 1973-03-23 | 1976-08-03 | Hoechst Aktiengesellschaft | Process for the preparation of discharge effects on dyeings or prints made with disperse dyes on flat-surface textile structures of synthetic fibers |
US4147509A (en) * | 1977-01-29 | 1979-04-03 | Basf Aktiengesellschaft | Pressure-sensitive recording material |
US4603202A (en) * | 1983-10-14 | 1986-07-29 | Basf Aktiengesellschaft | Fluoran colorants for recording systems |
US4958021A (en) * | 1987-07-25 | 1990-09-18 | Basf Aktiengesellschaft | Benzopyran derivatives |
WO2008038645A1 (en) | 2006-09-29 | 2008-04-03 | Nippon Paper Industries Co., Ltd. | Heat-sensitive recording material |
US8857337B2 (en) | 2013-03-14 | 2014-10-14 | Accolade Group Inc. | Method for printing an image on the under peak of a baseball cap and baseball cap |
US20150337488A1 (en) * | 2013-02-01 | 2015-11-26 | Soochow University | A METHOD OF PHOTOCATALYTIC WHITE DISCHARGE PRINTING FOR ACHIEVING PATTERNS ON TEXTILES (As Amended) |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB342333A (en) * | 1929-10-26 | 1931-01-26 | British Celanese | Improvements in or relating to the production of pattern effects on materials made of or containing cellulose esters or ethers |
US1864582A (en) * | 1931-12-10 | 1932-06-28 | Susquehanna Silk Mills | Color discharge printing |
US2109709A (en) * | 1936-06-05 | 1938-03-01 | John W Pribble | Brake |
US2248128A (en) * | 1939-05-10 | 1941-07-08 | Celanese Corp | Production of pattern effects on textile materials |
US2409980A (en) * | 1943-08-28 | 1946-10-22 | Eastman Kodak Co | Composition for discharge printing |
US2435658A (en) * | 1944-07-19 | 1948-02-10 | Celanese Corp | Illuminated discharge effects upon acetate fabrics |
US2862785A (en) * | 1953-01-01 | 1958-12-02 | British Celanese | Cellulose triacetate fabrics of improved safe ironing temperature and process of heat treatment to obtain said fabrics |
US2874022A (en) * | 1956-06-14 | 1959-02-17 | Ciba Company Inc | Composition and process for application and discharge printing |
-
0
- US US3103404D patent/US3103404A/en not_active Expired - Lifetime
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB342333A (en) * | 1929-10-26 | 1931-01-26 | British Celanese | Improvements in or relating to the production of pattern effects on materials made of or containing cellulose esters or ethers |
US1864582A (en) * | 1931-12-10 | 1932-06-28 | Susquehanna Silk Mills | Color discharge printing |
US2109709A (en) * | 1936-06-05 | 1938-03-01 | John W Pribble | Brake |
US2248128A (en) * | 1939-05-10 | 1941-07-08 | Celanese Corp | Production of pattern effects on textile materials |
US2409980A (en) * | 1943-08-28 | 1946-10-22 | Eastman Kodak Co | Composition for discharge printing |
US2435658A (en) * | 1944-07-19 | 1948-02-10 | Celanese Corp | Illuminated discharge effects upon acetate fabrics |
US2862785A (en) * | 1953-01-01 | 1958-12-02 | British Celanese | Cellulose triacetate fabrics of improved safe ironing temperature and process of heat treatment to obtain said fabrics |
US2874022A (en) * | 1956-06-14 | 1959-02-17 | Ciba Company Inc | Composition and process for application and discharge printing |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3923457A (en) * | 1972-10-12 | 1975-12-02 | Hoechst Ag | Mixtures of fixing auxiliaries containing novel dye carrier |
US3972677A (en) * | 1973-03-23 | 1976-08-03 | Hoechst Aktiengesellschaft | Process for the preparation of discharge effects on dyeings or prints made with disperse dyes on flat-surface textile structures of synthetic fibers |
US4147509A (en) * | 1977-01-29 | 1979-04-03 | Basf Aktiengesellschaft | Pressure-sensitive recording material |
US4603202A (en) * | 1983-10-14 | 1986-07-29 | Basf Aktiengesellschaft | Fluoran colorants for recording systems |
US4958021A (en) * | 1987-07-25 | 1990-09-18 | Basf Aktiengesellschaft | Benzopyran derivatives |
WO2008038645A1 (en) | 2006-09-29 | 2008-04-03 | Nippon Paper Industries Co., Ltd. | Heat-sensitive recording material |
US20150337488A1 (en) * | 2013-02-01 | 2015-11-26 | Soochow University | A METHOD OF PHOTOCATALYTIC WHITE DISCHARGE PRINTING FOR ACHIEVING PATTERNS ON TEXTILES (As Amended) |
US9797089B2 (en) * | 2013-02-01 | 2017-10-24 | Soochow University | Method of photocatalytic white discharge printing for achieving patterns on textiles |
US8857337B2 (en) | 2013-03-14 | 2014-10-14 | Accolade Group Inc. | Method for printing an image on the under peak of a baseball cap and baseball cap |
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