US2017120A - Production of discharge effects - Google Patents
Production of discharge effects Download PDFInfo
- Publication number
- US2017120A US2017120A US605115A US60511532A US2017120A US 2017120 A US2017120 A US 2017120A US 605115 A US605115 A US 605115A US 60511532 A US60511532 A US 60511532A US 2017120 A US2017120 A US 2017120A
- Authority
- US
- United States
- Prior art keywords
- materials
- cellulose
- leuco
- zinc
- vat
- 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
Links
- 230000000694 effects Effects 0.000 title description 9
- 238000004519 manufacturing process Methods 0.000 title description 5
- 239000000463 material Substances 0.000 description 22
- 229920002678 cellulose Polymers 0.000 description 14
- 150000002736 metal compounds Chemical class 0.000 description 11
- 229920002301 cellulose acetate Polymers 0.000 description 10
- 239000001913 cellulose Substances 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 9
- 239000000203 mixture Substances 0.000 description 8
- -1 alkali metal salts Chemical class 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 230000001681 protective effect Effects 0.000 description 7
- 150000003752 zinc compounds Chemical class 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 6
- CAAIULQYGCAMCD-UHFFFAOYSA-L zinc;hydroxymethanesulfinate Chemical compound [Zn+2].OCS([O-])=O.OCS([O-])=O CAAIULQYGCAMCD-UHFFFAOYSA-L 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 5
- 238000011282 treatment Methods 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 4
- 150000004056 anthraquinones Chemical class 0.000 description 4
- 239000000084 colloidal system Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 3
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 229920003086 cellulose ether Polymers 0.000 description 3
- 229940097275 indigo Drugs 0.000 description 3
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 210000002268 wool Anatomy 0.000 description 3
- 235000005074 zinc chloride Nutrition 0.000 description 3
- 239000011592 zinc chloride Substances 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 239000007900 aqueous suspension Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- RZVHIXYEVGDQDX-UHFFFAOYSA-N 9,10-anthraquinone Chemical group C1=CC=C2C(=O)C3=CC=CC=C3C(=O)C2=C1 RZVHIXYEVGDQDX-UHFFFAOYSA-N 0.000 description 1
- 229920002955 Art silk Polymers 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 241000152727 Salix caprea subsp. caprea Species 0.000 description 1
- 241000978776 Senegalia senegal Species 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000001339 alkali metal compounds Chemical class 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 230000001914 calming effect Effects 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 229960001777 castor oil Drugs 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000003518 caustics Substances 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
- 238000007599 discharging Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- QJQZEJFUIOWFMS-UHFFFAOYSA-N formaldehyde;sulfanediol Chemical compound O=C.OSO QJQZEJFUIOWFMS-UHFFFAOYSA-N 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000010977 jade Substances 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 1
- 229960003656 ricinoleic acid Drugs 0.000 description 1
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- VYGBQXDNOUHIBZ-UHFFFAOYSA-L sodium formaldehyde sulphoxylate Chemical compound [Na+].[Na+].O=C.[O-]S[O-] VYGBQXDNOUHIBZ-UHFFFAOYSA-L 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000000984 vat dye Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
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
- This invention relates to the coloration of textile materials, more particularly materials made of or containing cellulose acetate or other cellulose esters or ethers or animal fibres, for example 5 wool and silk.
- the insoluble zinc compounds are compatible with zinc formaldehyde sulphoxylate, and at the same time are capable of coloring cellulose acetatematerials. They may therefore be employed in admixture with zinc formaldehyde sulphoxylate for the purpose of producing on cellulose acetate materials valuable discharge effects illuminated with vat dyestuffs.
- the zinc compounds of leuco vat dyestuffs and also other insoluble metal compounds of vat dyestuifs are generally applicable in the coloration of cellulose acetate materials.
- Other cellulose esters and also cellulose others may be colored in the same manner and likewise animal fibres, for example'wool and silk.
- the present invention comprises the coloration of materials consisting of or containing cellulose acetate or other organic derivatives of cellulose or animal fibres by the application of vat dyestuffs in the form of insoluble metal derivatives of their leuco compounds.
- Insoluble metal compounds of leuco vat dyestuffs exhibit the important advantage that they are not strongly alkaline and may be applied under either neutral or even moderately acid conditions. They may therefore be utilized,
- the zinc compounds of leuco vat dyestuffs have been found particularly convenient for application in accordance with the present invention, but other insoluble metal compounds may 15 be utilized if desired, for example compounds with cadmium, aluminium, tin, lead or iron.
- These insoluble metal compounds of leuco vat dyestuffs are conveniently prepared by interaction between the alkali metal salts of the leuco compounds and an appropriate metal salts, preferably such as are water-soluble.
- the dyestufl in question may be vatted with sodium hydrosulphite or other reducing agent and just sufficient caustic alkali to yield a solution of the leuco compound.
- the solution thus obtained may be treated with an aqueous solution of the appropriate metal salt, for example a concentrated solution of zinc chloride, whereby the desired metal compound of the leuco vat 30 dyestuif may be precipitated.
- the appropriate metal salt for example a concentrated solution of zinc chloride
- vat dyestuffs havingaflinity for the materials to be colored may be applied by the new process. Particular mention may be made, especially for the coloration of cellulose ester and ether materials,'of the anthraquinone vat dyes containing one anthraquinone residue described in U. S. application S. No. 583,392 filed 26th December, 1931 and of indigoid dyestuffs, especially the indigoid dyestuffs described in U. S. application S. No. 583,406 filed 26th December, 1931, and derivatives of indigo and thioindigo.
- he insoluble metal compounds of leuco vat dyestuffs are conveniently applied to the materials in the form of aqueous suspensions or dispersions which may be prepared by any convenient means.
- the metal compounds may be directly converted into aqueous suspensions or dispersions by mechanical treatment or by treatment with dispersing agents 0 and/or protective colloids or by the combination of these treatments.
- a preparation adapted for application by printing may be made simply by stirring or grinding the metal compound with gumarabic or other thickening agent.
- a solution oian alkali salt oi a leuco compound may be precipitated with zinc chloride or other appropriate metal salt in .the presence oi a dispersing loid.
- dispersion is eiiected in neutral or somewhat acid media, and dispersing agents or protective colloids, where employed, should be stable and capable oi exerting their or protective action in such media.
- dispersing agents or protective colloids of this character may be mentioned highly sulphonated compounds such as .highly sulphonated castoroil, sulpho aromatic fatty acids for example sulpho-naphthaline ricinoleic acid (see U. 8. Patents Nos. 1,840,572 and 1,694,413), basic agents soluble in acid media for example oleyl diethyl ethylene diamine or other basic derivativeoiaiattyacidalsostarcheaginnaglue, gelatin and the like.
- the dispersions or suspensions may bepreparedinconcentratediormadaptedto yield by dilution, with orwithou't addition of thickening agents or further agents preparations Wehavetoundthatitisnotessentialtoprepare theinsoluble metaloileucovat dyestuflspriortoapplicationtothematerlalas,it desired,theymaybe i'ormed onthematerial itself.
- Thbmethodoicarryingcutthe newprocehismoreparticularlyappiicable whencolorations are to be callybyprintingorotberwlse.
- celiuloseesterorethermaterialsooloredin lidesiredhoweveathemetalmay' agent and/or a protective colaocordame with the present invention may consist, for instance, of cellulose acetate as previously mentioned or of cellulose iormate, propionate or butyrate or the products obtainable by esteriiying cellulosic materials while retaining their fibrous 6 form, for example the product known as-immunised cotton" obtained by treating alkali cellulose with para-toluene-sulphonic chloride, or
- the invention 10 is also applicable, as previously indicated. to the coloration of wool, silk and other animal iibres.
- Mixed materials comprising two or more types of the foregoing materials, tor example cellulose acetate and silk, or comprising one of the foregoing 1.; materials and another textilematerial, for example cotton or the regenerated cellulose type of artificial silk. may likewise be colored by the new
- coloring materials consist'oi or contain cellulose esters or ethers
- the insoluble metal compounds or ieuco vat dyestuils may with advantage be applied in conjunction with alcohols, e. g. ethyl alcohol, phenols, e. g. hydroquinone, or other swelling agents for the material under treatment,
- the discharge composition may contain anthraquinone or other agents facilitating discharge with reducing agents.
- the invention is illustratedbut not limited by so.
- sample 1 sample 1 'Amaterialofcelluloaeacetateora mixtureoi' cellulose acetateandsilkisprintedll 'againwashedanddried.
- the sine carbonate h conveniently prepared as a20% pastebyprecipitationoisincsulphatewith sodaashinaqueousaohition.
- Acelluloseacetateiabric dyedwithadischarges'sahle calming matter is ingprinting paste:
- the zinc compound of the leuco vat dyestufl may be prepared in the following manner:
- Process for the production of discharge effects on materials comprising organic derivatives of cellulose which comprises applying locally thereto a discharge composition containing zinc employed, for example, Ciba scarlet G, Durindone formaldehyde sulphoxylate and a water-insoluble metal compound of a leuco vat dyestufl.
- a discharge composition containing zinc employed, for example, Ciba scarlet G, Durindone formaldehyde sulphoxylate and a water-insoluble metal compound of a leuco vat dyestufl.
- Process for the production of discharge effects on materials comprising cellulose acetate which comprises applying locally thereto a discharge composition containing zinc formaldehyde sulphoxylate and a zinc compound of a leuco vat dyestufi of the indigoid series.
- Process for the production of discharge effects on materials comprising cellulose acetate which comprises applying locally thereto a discharge composition containing zinc formaldehyde sulphoxylate and a zinc compound of a leuco compound of an anthraquinone dyestufi containing a 20 single anthraquinone nucleus.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Coloring (AREA)
Description
Patented Oct. 15, 1935 UNITEDJ STATES PATENT OFFICE rRon o'noN or DISCHARGE EFFECT ware No Drawing. Application April 13, 1932, Serial No. 605,115. In Great Britain May 19, 1931 4 Claims.
This invention relates to the coloration of textile materials, more particularly materials made of or containing cellulose acetate or other cellulose esters or ethers or animal fibres, for example 5 wool and silk.
It is well known that discharge effects may readily beproduced upon colored cotton materials by local application thereto of compositions containing sodium formaldehyde sulphoxylate. Fast colored discharges may be produced by this process by incorporatingein the discharge composition leuco compounds of vat dyestuffs in the form of alkali metal salts. In the case of cellulose acetate materials however discharge effects are'much less readily produced by means of discharging agents comprising sodium or other alkali metal formaldehyde sulphoxylate. With the aid of zinc formaldehyde sulphoxylate it is how- We have now observed that, as opposed to the water-soluble alkali metal compounds of leuco vat dyestuffs, the insoluble zinc compounds are compatible with zinc formaldehyde sulphoxylate, and at the same time are capable of coloring cellulose acetatematerials. They may therefore be employed in admixture with zinc formaldehyde sulphoxylate for the purpose of producing on cellulose acetate materials valuable discharge effects illuminated with vat dyestuffs. We have found in fact that the zinc compounds of leuco vat dyestuffs and also other insoluble metal compounds of vat dyestuifs are generally applicable in the coloration of cellulose acetate materials. Other cellulose esters and also cellulose others may be colored in the same manner and likewise animal fibres, for example'wool and silk.
Broadly, therefore, the present invention comprises the coloration of materials consisting of or containing cellulose acetate or other organic derivatives of cellulose or animal fibres by the application of vat dyestuffs in the form of insoluble metal derivatives of their leuco compounds. Insoluble metal compounds of leuco vat dyestuffs exhibit the important advantage that they are not strongly alkaline and may be applied under either neutral or even moderately acid conditions. They may therefore be utilized,
as explained above, for the coloration of discharges produced by means of zinc formaldehyde 5 sulphoxylate or by means of other heavy metal aldehyde or ketone sulphoxylates, and further they may be used to color materials, for instance cellulose esters and animal fibres, which are liable to damage by strongly alkaline baths or printing 10 compositions.
The zinc compounds of leuco vat dyestuffs have been found particularly convenient for application in accordance with the present invention, but other insoluble metal compounds may 15 be utilized if desired, for example compounds with cadmium, aluminium, tin, lead or iron. These insoluble metal compounds of leuco vat dyestuffs are conveniently prepared by interaction between the alkali metal salts of the leuco compounds and an appropriate metal salts, preferably such as are water-soluble. For instance, the dyestufl in question may be vatted with sodium hydrosulphite or other reducing agent and just sufficient caustic alkali to yield a solution of the leuco compound. 25 The solution thus obtained, if desired after filtration, may be treated with an aqueous solution of the appropriate metal salt, for example a concentrated solution of zinc chloride, whereby the desired metal compound of the leuco vat 30 dyestuif may be precipitated.
A wide range of vat dyestuffs havingaflinity for the materials to be colored may be applied by the new process. Particular mention may be made, especially for the coloration of cellulose ester and ether materials,'of the anthraquinone vat dyes containing one anthraquinone residue described in U. S. application S. No. 583,392 filed 26th December, 1931 and of indigoid dyestuffs, especially the indigoid dyestuffs described in U. S. application S. No. 583,406 filed 26th December, 1931, and derivatives of indigo and thioindigo.
he insoluble metal compounds of leuco vat dyestuffs, are conveniently applied to the materials in the form of aqueous suspensions or dispersions which may be prepared by any convenient means. For example, the metal compounds may be directly converted into aqueous suspensions or dispersions by mechanical treatment or by treatment with dispersing agents 0 and/or protective colloids or by the combination of these treatments. Thus a preparation adapted for application by printing may be made simply by stirring or grinding the metal compound with gumarabic or other thickening agent.
7 or .protective colloith, liguids or -adaptedfordyeingandprintingmlrposes.
iormedin the presence of mt. and/or protective colloids and suitable -1or dyeing and. printing directly obtained. Thus, a solution oian alkali salt oi a leuco compound may be precipitated with zinc chloride or other appropriate metal salt in .the presence oi a dispersing loid.
Preferably dispersion is eiiected in neutral or somewhat acid media, and dispersing agents or protective colloids, where employed, should be stable and capable oi exerting their or protective action in such media. As examples oi dispersing agentsor protective colloids of this character may be mentioned highly sulphonated compounds such as .highly sulphonated castoroil, sulpho aromatic fatty acids for example sulpho-naphthaline ricinoleic acid (see U. 8. Patents Nos. 1,840,572 and 1,694,413), basic agents soluble in acid media for example oleyl diethyl ethylene diamine or other basic derivativeoiaiattyacidalsostarcheaginnaglue, gelatin and the like.
If desired the dispersions or suspensions may bepreparedinconcentratediormadaptedto yield by dilution, with orwithou't addition of thickening agents or further agents preparations Wehavetoundthatitisnotessentialtoprepare theinsoluble metaloileucovat dyestuflspriortoapplicationtothematerlalas,it desired,theymaybe i'ormed onthematerial itself. For instance, the unreduced vat dyestuit inadmi xturewithareducingagentandametal oxide, carbonate, or other compoimdmaybe applied to the material and the latter then steamed, whereby the metal compound oi the leuco vat dyestufl isiormedinsitia ln'thisprocusthe.
presenceoistrmaikaliesshouldolooursebe avoided,asotherwhethereouiredmetalcompoundmay notbetormed. Thbmethodoicarryingcutthe newprocehismoreparticularlyappiicable whencolorations are to be callybyprintingorotberwlse.
The applicaflon of the or dispersions of the insolublemetai oileueo .vatdyatuii'stothematerialsmaybeeilected 'in-anydairedinannu,iorexampleby.dyeing,-
padding, or printingallovenoriocallybypu-inting, stencillingor other-method oilocal application. As explained previously however the vinventionhasbeeni'oundotgreatestvaluein etlectiimci'ilorat'irlisliyprintingorothei'modeoi localapplicaidmandmoreparticularlywhenthe vatdyestuitsaretobeusedi'ortheoolm'ationoi l dischargeaproduced by meansof sine formaldezbydesuiphosylatem'othermctalaldehydeor ketonesulphoaylatmwhicharedetrhnentaliyeiiectedbyeausiiealkali, Particularinentionmay bemadeoi'theapplicationotthemetalcompoimdsi'ortheilhimination'otsinci'ormaldehyde be'washed, soapedorsuhjectedto any other desirediinishingtreailnent.
celiuloseesterorethermaterialsooloredin lidesiredhoweveathemetalmay' agent and/or a protective colaocordame with the present invention may consist, for instance, of cellulose acetate as previously mentioned or of cellulose iormate, propionate or butyrate or the products obtainable by esteriiying cellulosic materials while retaining their fibrous 6 form, for example the product known as-immunised cotton" obtained by treating alkali cellulose with para-toluene-sulphonic chloride, or
they may consist of ethyl, methyl or benzyl cellulose or other ether of cellulose. The invention 10 is also applicable, as previously indicated. to the coloration of wool, silk and other animal iibres.
. Mixed materials comprising two or more types of the foregoing materials, tor example cellulose acetate and silk, or comprising one of the foregoing 1.; materials and another textilematerial, for example cotton or the regenerated cellulose type of artificial silk. may likewise be colored by the new When coloring materials consist'oi or contain cellulose esters or ethers the insoluble metal compounds or ieuco vat dyestuils may with advantage be applied in conjunction with alcohols, e. g. ethyl alcohol, phenols, e. g. hydroquinone, or other swelling agents for the material under treatment, Again when colored discharge eii'ects are to be produced the discharge composition may contain anthraquinone or other agents facilitating discharge with reducing agents.
The invention is illustratedbut not limited by so.
the tollifaing examples: sample 1 'Amaterialofcelluloaeacetateora mixtureoi' cellulose acetateandsilkisprintedll 'againwashedanddried.
The sine carbonate h conveniently prepared as a20% pastebyprecipitationoisincsulphatewith sodaashinaqueousaohition.
trample 2 Acelluloseacetateiabric dyedwithadischarges'sahle calming matter is ingprinting paste:
zincsaitoi'theleucocompoundotcibayelprinted with the followlowG 20 llethylated spirits. 10 Water 5 Gumarabicifl 40 Zinci'ormaldehydesuiphosylate. 28
. p r a e Afterprintingthematerialisageiiiorbminutes andthenehromemwashemsoapedand flnally rinsedand-dried. In thismanner iastyeliow dischargeeiiectsmaybeobtaineduponacolcred -lnplaceoi'thezinesaltoitheleucocanpotmd otclbayeliowqthecorrespondingsincoom poimdspreparedfromothervatdyestuiismaybe u. bLtAL HiNh' ct UYuwc; iLUlU TREATMENT at CHEWCAL MODIFI- 6 4CATION OF TEXTILES & FIBERS,
red Y, Algol violet BBN, Indigo LL, Indigo LII/2R and Caledofi jade green.
The zinc compound of the leuco vat dyestufl may be prepared in the following manner:
10 parts of dyestufi powder (e. g. Ciba yellow G) 8 parts caustic soda and 400 parts of water are well mixed and heated to 60 C. About 16 parts sodium hydrosulphite are added with good stirring until a clear vat is obtained. This solution is filtered to remove any insoluble matter and whilst still warm a solution of 10 parts of zinc chloride in 30-40 parts of water is added. The zinc salt of the leuco compound separates as a flocculent cream-colored precipitate and is filtered oil, washed with a very small quantity of water and retained as an aqueous paste.
What we claim and desire to secure by Letters Patent is: a
1. Process for the production of discharge effects on materials comprising organic derivatives of cellulose which comprises applying locally thereto a discharge composition containing zinc employed, for example, Ciba scarlet G, Durindone formaldehyde sulphoxylate and a water-insoluble metal compound of a leuco vat dyestufl.
2. Process for the production of discharge effects on materials comprising cellulose acetate which comprises applying locally thereto a discharge composition containing zinc formaldehyde sulphoxylate and a zinc compound of a leuco vat dyestufi.
3. Process for the production of discharge effects on materials comprising cellulose acetate which comprises applying locally thereto a discharge composition containing zinc formaldehyde sulphoxylate and a zinc compound of a leuco vat dyestufi of the indigoid series.
4. Process for the production of discharge effects on materials comprising cellulose acetate which comprises applying locally thereto a discharge composition containing zinc formaldehyde sulphoxylate and a zinc compound of a leuco compound of an anthraquinone dyestufi containing a 20 single anthraquinone nucleus.
GEORGE HOLLAND ELLIS. JOHN ALLAN.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2017120X | 1931-05-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2017120A true US2017120A (en) | 1935-10-15 |
Family
ID=10896177
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US605115A Expired - Lifetime US2017120A (en) | 1931-05-19 | 1932-04-13 | Production of discharge effects |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2017120A (en) |
-
1932
- 1932-04-13 US US605115A patent/US2017120A/en not_active Expired - Lifetime
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