PL37352B1 - - Google Patents
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- PL37352B1 PL37352B1 PL37352A PL3735254A PL37352B1 PL 37352 B1 PL37352 B1 PL 37352B1 PL 37352 A PL37352 A PL 37352A PL 3735254 A PL3735254 A PL 3735254A PL 37352 B1 PL37352 B1 PL 37352B1
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- Prior art keywords
- printing
- dye
- printing ink
- substances
- dyes
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- 239000000975 dye Substances 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 2
- 239000004753 textile Substances 0.000 claims description 2
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 150000004985 diamines Chemical class 0.000 claims 1
- 239000003973 paint Substances 0.000 claims 1
- 239000000976 ink Substances 0.000 description 9
- 239000000126 substance Substances 0.000 description 8
- UHOKSCJSTAHBSO-UHFFFAOYSA-N indanthrone blue Chemical compound C1=CC=C2C(=O)C3=CC=C4NC5=C6C(=O)C7=CC=CC=C7C(=O)C6=CC=C5NC4=C3C(=O)C2=C1 UHOKSCJSTAHBSO-UHFFFAOYSA-N 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 5
- 238000001704 evaporation Methods 0.000 description 5
- 230000008020 evaporation Effects 0.000 description 5
- 239000000835 fiber Substances 0.000 description 5
- 239000000984 vat dye Substances 0.000 description 5
- 235000019239 indanthrene blue RS Nutrition 0.000 description 4
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000004043 dyeing Methods 0.000 description 3
- 230000003165 hydrotropic effect Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- 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 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- XWGJFPHUCFXLBL-UHFFFAOYSA-M rongalite Chemical compound [Na+].OCS([O-])=O XWGJFPHUCFXLBL-UHFFFAOYSA-M 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- ZLHGTHCCYUEAIK-UHFFFAOYSA-N 5,7-dibromo-2-(5,7-dibromo-3-hydroxy-1H-indol-2-yl)indol-3-one Chemical compound [O-]c1c([nH]c2c(Br)cc(Br)cc12)C1=[NH+]c2c(cc(Br)cc2Br)C1=O ZLHGTHCCYUEAIK-UHFFFAOYSA-N 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Natural products CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 description 1
- KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical class C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- ZTWQZJLUUZHJGS-UHFFFAOYSA-N Vat Yellow 4 Chemical compound C12=CC=CC=C2C(=O)C2=CC=C3C4=CC=CC=C4C(=O)C4=C3C2=C1C=C4 ZTWQZJLUUZHJGS-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 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 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical class C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 229960001506 brilliant green Drugs 0.000 description 1
- HXCILVUBKWANLN-UHFFFAOYSA-N brilliant green cation Chemical compound C1=CC(N(CC)CC)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](CC)CC)C=C1 HXCILVUBKWANLN-UHFFFAOYSA-N 0.000 description 1
- GTRGJJDVSJFNTE-UHFFFAOYSA-N chembl2009633 Chemical compound OC1=CC=C2C=C(S(O)(=O)=O)C=CC2=C1N=NC1=CC=CC=C1 GTRGJJDVSJFNTE-UHFFFAOYSA-N 0.000 description 1
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 description 1
- 229960001231 choline Drugs 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003752 hydrotrope Substances 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- -1 leucine compound Chemical class 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 239000000693 micelle Substances 0.000 description 1
- 150000002895 organic esters Chemical class 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000005185 salting out Methods 0.000 description 1
- LJRGBERXYNQPJI-UHFFFAOYSA-M sodium;3-nitrobenzenesulfonate Chemical compound [Na+].[O-][N+](=O)C1=CC=CC(S([O-])(=O)=O)=C1 LJRGBERXYNQPJI-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- NVBFHJWHLNUMCV-UHFFFAOYSA-N sulfamide Chemical class NS(N)(=O)=O NVBFHJWHLNUMCV-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 1
- JXUKQCUPTNLTCS-UHFFFAOYSA-N vat green 1 Chemical compound C1=CC=C[C]2C(=O)C(C3=C45)=CC=C4C(C4=C67)=CC=C7C(=O)[C]7C=CC=CC7=C6C=C(OC)C4=C5C(OC)=CC3=C21 JXUKQCUPTNLTCS-UHFFFAOYSA-N 0.000 description 1
Description
Wynalazek dotyczy farby drukarskiej do dru¬ ku barwnikami kadziowymi, dajacymi najtrwal¬ sze efekty w druku tkanin.Barwniki kadziowe stanowia zwiazki o du¬ zym ciezarze czasteczkowym, co powoduje nie¬ calkowite ich adsorbowanie przez wlókno.Wskutek tego pewna czesc cennego barwnika zostaje bezpowrotnie stracona w koncowych okresach wykonczania tkanin drukowanych, a mianowicie podczas utleniania, mydlenia i plu¬ kania. Z tych wzgledów do farb drukarskich do druku barwnikami kadziowymi dodawano róznych substancji wplywajacych na zmniejsze¬ nie strat barwnika. Dzialanie substancji korzyst¬ nie wplywajacych w procesie utrwalania barw¬ nika kadziowego moze byc rozmaiter Moga to byc substancje higroskopijne i (lub) rozpraszaja¬ ce, które pobierajac wilgoc z pary wodnej pod¬ czas parowania ulatwiaja proces rozpuszczania sie leukozwiazku barwnika lub jego rozproszenie a tym samym przenikanie stalych rozdrobnio- *) Wlasciciel patentu oswiadczyl, ze twórcami wy¬ nalazku sa tmgr iinz. Ignacy Jakobson i mgr inz. Wie¬ slaw Józefowicz. nych czastek barwnika w micele wlókna. Uzy¬ skuje sie przez to czesto poglebienie badz ozy¬ wienie wybarwienia, przy czym poszczególne barwniki kadziowe w stosunku do wymienio¬ nych substancji zachowuja sie róznie. Do tego celu stosuje sie gliceryne, glikol i jego pochodne eterowe, dwuetylenoglikol, tiodwuetylenoglikol, jego produkty utlenienia, oraz oksyalkiloaminy, np. trójeltanoloamine.Obok wymienionego rodzaju zwiazków znane jest stosowanie substancji wplywajacych przy¬ spieszajaco na utrwalenie leukozwiazku barw¬ nika podczas procesu parowania, np. pochodnych antrachinonu, choliny lub betainy. Wreszcie znane jest równiez stosowanie substancji powo¬ dujacych zwiekszenie rozpuszczalnosci leuko- zwiazków barwników, np. soli sodowej kwasu benzosulfanilowego, pochodnych benzotiazolu, niektórych sulfoamidów, estrów organicznych kwasu borowego lub mocznika. Substancje te, zwlaszcza mocznik, wywoluja specznienie i roz¬ luznienie wlókna oraz obnizaja lepkosc farby drukarskiej podczas procesu- parowania, zwla¬ szcza w tych przypadkach, gdy zastosuje sie du-** ze stezenie Jych substancji, np. 1^,— 15% w sto- sunku7^|v^a^vfarbv ó^^aAltfej.Stwierdzono\ ze w* wielu prz^adkach poza¬ dane efekty hydrotropowe uzyskuje sie przez wprowadzenie do farby drukarskiej dwucyja- nodwuamidu, który ulatwia adsorbcje leuko- zwiazku barwnika przez wlókna, dzieki czemu uzyskuje sie zwiekszenie intensywnosci wybar- wienia oraz zmniejszenie strat barwnika. Ko¬ rzystne efekty hydrotropowe zostaly stwierdzo¬ ne przy druku nastepujacymi barwnikami ka¬ dziowymi; Zielen indamtrenowa brylantowa B, Oranz indantrenowy brylantowy RKN, Zielen indantrenowa brylantowa 4G, Zlocista zólcien kadziowa ZH, Ciemny blekit indantrenowy BOA, Blekit kadziowy 4B, Szkarlat algolowy GGM, Róz cibanonowy 3B oraz Fiolet sandotrenowy N8RB.Stwierdzono równiez, ze po wprowadzeniu dwucyjanodwuamidu do farby drukarskiej w niektórych przypadkach, np. przy zastosowaniu Blekitu helantrenowego RS, uzyskuje sie znacz¬ ne skrócenie czasu parowania, potrzebnego do utrwalenia leukozwiazku tego barwnika na wlóknie, przy czym przy tej samej recepturze skraca sie wyjatkowo dlugi czas parowania z 15 na 4,5 minuty, co umozliwia zastosowanie tego barwnika do druku wraz z innymi barwnikami indantrenowymi, posiadajacymi krótszy czas parowania.Ilosc dwucyjanodwuamidu potrzebna do otrzy¬ mania okreslonej intensywnosci wybarwienia przy uzyciu równiez okreslonej ilosci barwnika w farbie drukarskiej jest stosunkowo mniejsza w porównaniu z innymi zwiazkami hydrotropo- wymi, np. przy uzyciu mocznika. Wystarcza do¬ danie 25 — 30 g dwucyjanodwuamidu rta jeden kg farby drukarskiej, przy czym ze wzgledu na dzialanie wysalajace, które niekiedy wystepuje, nalezy dwucyjanodwuamid wprowadzac do ozie¬ bionej farby w koncowym etapie jej nastawia¬ nia. Dotychczas dodawano srodków hydrotropo- wych w ilosci powyzej 50 g na 1 kg farby dru¬ karskiej.Ponizej podane sa przyklady skladników farby drukarskiej wedlug wynalazku.Przyklad I. 70 g Zieleni indantrenowej brylantowej B, 80 g gliceryny, 500 g zageszczal- nika skrobiowego, 80 g potazu, 60 g rongalitu, 30 g dwucyjanodwuamidu, 180 g wody.Przyklad II. 75 g Blekitu helantrenowe¬ go RS w pascie, 30 g spirytusu, 508 g dekstry¬ ny 2 : 1, 267 g lugu sodowego 48°Be, 40 g ron¬ galitu 1:1, 5 g Nitrolu S, 25 g dwucyjanodwua¬ midu, 50 g wody. PLThe invention relates to a printing ink for printing with vat dyes, which give the most durable effects in textile printing. Vat dyes are compounds with a high molecular weight, which causes their incomplete adsorption by the fiber. As a result, some valuable dye is irretrievably lost. in the final stages of the finishing of printed fabrics, namely during oxidation, soaping and rinsing. For these reasons, various substances were added to the printing inks for printing with vat dyes, reducing the loss of the dye. The action of substances that favorably influence the process of fixing the vat dye may be various, it may be hygroscopic and / or diffusing substances which, by drawing moisture from water vapor during evaporation, facilitate the dissolution of the dye leuco compound or its dispersion, and thus the very penetration of solid fineness- *). The proprietor of the patent stated that the inventors are tmgr iinz. Ignacy Jakobson and MSc Wieśław Józefowicz. dye particles in the fiber micelles. This often results in a deepening or an intensification of the dyeing, with individual vat dyes behaving differently in relation to the substances mentioned. For this purpose, glycerol, glycol and its ether derivatives, diethylene glycol, thiodiethylene glycol, its oxidation products, and oxyalkylamines, e.g. triethanolamine are used. Apart from the compounds mentioned, it is known to use substances which accelerate the fixation of the leukosol compound during the dyeing process, for example anthraquinone, choline or betaine derivatives. Finally, it is also known to use substances which increase the solubility of dye leuco compounds, for example sodium benzosulfanilic acid, benzothiazole derivatives, some sulfamides, organic esters of boric acid or urea. These substances, especially urea, cause the fibers to swell and loosen, and reduce the viscosity of the ink during the evaporation process, especially in those cases when a high concentration of their substances is used, e.g. 1% - 15%. It has been found that in many examples the hydrotropic effects are obtained by introducing a dihydrotrope into the printing ink, which facilitates the adsorption of the dye leucine compound by the fibers thus increasing the intensity of staining and reducing the loss of dye. Advantageous hydrotropic effects have been found in printing with the following carbonaceous dyes; Indanthrene brilliant green B, indanthrene brilliant orange RKN, indanthrene brilliant green 4G, vat golden yellow ZH, dark indanthrene blue BOA, vat blue 4B, scarlate algae GGM, cyanonic pink 3B, and 8 cyanone cyanide. In some cases, e.g. with the use of Helanthrene Blue RS, the evaporation time needed to fix the leuco-compound of this dye on the fiber is significantly reduced, while for the same formulation the exceptionally long evaporation time is shortened from 15 to 4.5 minutes , which makes it possible to use this dye for printing together with other indanthrene dyes, having a shorter evaporation time. The amount of di-cyanediamide needed to obtain a certain intensity of dyeing using also a certain amount of dye in the printing ink is relatively lower compared to other hydrotropic compounds, eg when using power disappears. It is sufficient to add 25-30 g of dibasic diamide mercury to one kg of printing ink, and due to the salting-out action which sometimes occurs, it is necessary to introduce the dibasic diamide into the quenched ink in the final stage of its adjustment. Up to now, amounts of hydrotropes in excess of 50 g per 1 kg of printing ink have been added. Below are examples of the components of the printing ink according to the invention. Example I. 70 g of Brilliant Indanthrene Green B, 80 g of glycerin, 500 g of starch thickener, 80 g of potassium, 60 g of rongalite, 30 g of dicyanodiamide, 180 g of water. Example II. 75 g of helanthrene blue RS in paste, 30 g of spirit, 508 g of dextrin 2: 1, 267 g of sodium liquor 48 ° Be, 40 g of rongalite 1: 1, 5 g of Nitrol S, 25 g of dithyanedinamide , 50 g of water. PL
Claims (2)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL37352B1 true PL37352B1 (en) | 1954-06-15 |
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