GB547059A - Improvements connected with the printing and colouring of materials - Google Patents
Improvements connected with the printing and colouring of materialsInfo
- Publication number
- GB547059A GB547059A GB327/40A GB32740A GB547059A GB 547059 A GB547059 A GB 547059A GB 327/40 A GB327/40 A GB 327/40A GB 32740 A GB32740 A GB 32740A GB 547059 A GB547059 A GB 547059A
- Authority
- GB
- United Kingdom
- Prior art keywords
- resin
- solution
- mixture
- stirred
- per cent
- 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
Links
- 238000004040 coloring Methods 0.000 title abstract 2
- 239000000203 mixture Substances 0.000 abstract 9
- 229920005989 resin Polymers 0.000 abstract 9
- 239000011347 resin Substances 0.000 abstract 9
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 abstract 6
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 abstract 4
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 abstract 4
- 239000001856 Ethyl cellulose Substances 0.000 abstract 3
- 239000005018 casein Substances 0.000 abstract 3
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 abstract 3
- 235000021240 caseins Nutrition 0.000 abstract 3
- 239000000839 emulsion Substances 0.000 abstract 3
- 229920001249 ethyl cellulose Polymers 0.000 abstract 3
- 235000019325 ethyl cellulose Nutrition 0.000 abstract 3
- RNJIWICOCATEFH-WCWDXBQESA-N (2e)-2-(1-oxobenzo[e][1]benzothiol-2-ylidene)benzo[e][1]benzothiol-1-one Chemical compound C1=CC=CC2=C(C(C(=C3/C(C4=C5C=CC=CC5=CC=C4S3)=O)/S3)=O)C3=CC=C21 RNJIWICOCATEFH-WCWDXBQESA-N 0.000 abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 abstract 2
- 229920000180 alkyd Polymers 0.000 abstract 2
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 abstract 2
- 239000006185 dispersion Substances 0.000 abstract 2
- 238000000227 grinding Methods 0.000 abstract 2
- QUBQYFYWUJJAAK-UHFFFAOYSA-N oxymethurea Chemical compound OCNC(=O)NCO QUBQYFYWUJJAAK-UHFFFAOYSA-N 0.000 abstract 2
- 229950005308 oxymethurea Drugs 0.000 abstract 2
- 239000010665 pine oil Substances 0.000 abstract 2
- 229920003002 synthetic resin Polymers 0.000 abstract 2
- 239000000057 synthetic resin Substances 0.000 abstract 2
- CGLDLDBFLNXMGE-MDZDMXLPSA-N 2-[(e)-2-(9,10-dioxoanthracen-2-yl)ethenyl]anthracene-9,10-dione Chemical compound C1=CC=C2C(=O)C3=CC(/C=C/C=4C=C5C(=O)C6=CC=CC=C6C(C5=CC=4)=O)=CC=C3C(=O)C2=C1 CGLDLDBFLNXMGE-MDZDMXLPSA-N 0.000 abstract 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical class [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 abstract 1
- 239000004233 Indanthrene blue RS Substances 0.000 abstract 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 1
- KQLYFVFFPVJGRM-NBTZWHCOSA-N azanium;(9z,12z)-octadeca-9,12-dienoate Chemical compound [NH4+].CCCCC\C=C/C\C=C/CCCCCCCC([O-])=O KQLYFVFFPVJGRM-NBTZWHCOSA-N 0.000 abstract 1
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 abstract 1
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 229920002678 cellulose Polymers 0.000 abstract 1
- 239000001913 cellulose Substances 0.000 abstract 1
- 229920003086 cellulose ether Polymers 0.000 abstract 1
- 239000000084 colloidal system Substances 0.000 abstract 1
- 239000003086 colorant Substances 0.000 abstract 1
- 239000000975 dye Substances 0.000 abstract 1
- 239000004744 fabric Substances 0.000 abstract 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 abstract 1
- 235000019239 indanthrene blue RS Nutrition 0.000 abstract 1
- 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 abstract 1
- 238000003801 milling Methods 0.000 abstract 1
- 238000002156 mixing Methods 0.000 abstract 1
- 239000003921 oil Substances 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 239000000049 pigment Substances 0.000 abstract 1
- 238000010992 reflux Methods 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 238000003756 stirring Methods 0.000 abstract 1
- 229920001567 vinyl ester resin Polymers 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- 239000008096 xylene Substances 0.000 abstract 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
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Paints Or Removers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
547,059. Synthetic resin dispersions. AMERICAN CYANAMID CO. Jan. 5, 1940, No. 327. Convention date, Jan. 21, 1939. [Class 1 (i)] [Also in Group IV] A coloured aqueous dispersion of a waterinsoluble synthetic resin for use in printing or otherwise colouring fibres and fabrics contains a minor proportion in relation to the resin of a cellulose ether substantially insoluble in water, but soluble in organic solvents. The resins may be of the alkyd, phenol-aldehyde, urea-aldehyde or polymerized vinyl ester types. The colours may be water-soluble dyes or may be pigments such as ultramarine, phthalocyanines, phosphotungstic or phosphomolybdic lakes of basic dyestuffs or coloured artificial resin complexes. In examples (1) dimethylolurea is refluxed with a large excess of cyclohexanol and part of the alcohol is removed to obtain a 50 per cent. solution of the resin in the alcohol, ethyl cellulose is dissolved in this solution and an oilmodified glycerophthalate resin is stirred in at 80-90‹ C., followed by addition of an ammoniacal casein solution with stirring to form a stable emulsion which is homogenized by passage through a colloid mill, aged for 24 hours, and pigmented by grinding therein a mixture of Vat brown RRD and oxidized Nigrosine; (2) ethyl cellulose is stirred into a 50 per cent. solution at 80‹ C. of a urea-aldehyde resin in cyclohexanol, prepared as in (1) and an oil-modified glycerophthalate resin is stirred into the mixture, a second mixture of the same 50 per cent. solution with dibutyl phthalate and the same oilmodified resin is made and the two mixtures are together emulsified with an ammoniacal casein solution or each is emulsified separately and the emulsions mixed; the complete emulsion is then pigmented with Vat brown RRD; (3) ethyl cellulose is stirred into pine oil and dibutyl phthalate at 80‹ C. and an oil modified glycerophthalate resin is stirred and milled into the mixture which is then pigmented by grinding into it a mixture of copper phthalocyanine and Anthraflavone G co-precipitated in presence of blanc fixe; a 50 per cent, solution in butanol of a ureaaldehyde resin made by refluxing dimethylolurea with butanol and a similar 50 per cent. solution in octanol are then milled in and the whole is emulsified with an ammoniacal casein solution; (4) benzyl cellulose is stirred into a mixture of pine oil, xylene and an alkyd-modified phenolformaldehyde resin at 80‹ C. and an air or heatconverting alkyd resin is stirred and milled into the mixture, which is then pigmented by milling into it a presscake of Indanthrene blue RS; a 50 per cent. solution in butanol of a urea-aldehyde resin and a similar 50 per cent. solution in octanol, both prepared as in (3), are then milled in and the mixture is emulsified with an ammonium linoleate solution. Nitroparaffins are also specified as blending solvents. Specification 344,458 is referred to.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US547059XA | 1939-01-21 | 1939-01-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB547059A true GB547059A (en) | 1942-08-12 |
Family
ID=21992958
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB327/40A Expired GB547059A (en) | 1939-01-21 | 1940-01-05 | Improvements connected with the printing and colouring of materials |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB547059A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4692188A (en) * | 1985-10-15 | 1987-09-08 | Xerox Corporation | Preparation of ink jet compositions |
-
1940
- 1940-01-05 GB GB327/40A patent/GB547059A/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4692188A (en) * | 1985-10-15 | 1987-09-08 | Xerox Corporation | Preparation of ink jet compositions |
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