DE3842054C2 - - Google Patents
Info
- Publication number
- DE3842054C2 DE3842054C2 DE19883842054 DE3842054A DE3842054C2 DE 3842054 C2 DE3842054 C2 DE 3842054C2 DE 19883842054 DE19883842054 DE 19883842054 DE 3842054 A DE3842054 A DE 3842054A DE 3842054 C2 DE3842054 C2 DE 3842054C2
- Authority
- DE
- Germany
- Prior art keywords
- dye
- preparations
- setting
- borate
- borax
- 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
- 239000000975 dye Substances 0.000 claims description 26
- 238000002360 preparation method Methods 0.000 claims description 17
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims description 7
- 229910021538 borax Inorganic materials 0.000 claims description 7
- 239000004328 sodium tetraborate Substances 0.000 claims description 7
- 235000010339 sodium tetraborate Nutrition 0.000 claims description 7
- 125000000129 anionic group Chemical group 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 150000003839 salts Chemical class 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 5
- 229910052938 sodium sulfate Inorganic materials 0.000 description 5
- 235000011152 sodium sulphate Nutrition 0.000 description 5
- 238000009835 boiling Methods 0.000 description 4
- 239000003995 emulsifying agent Substances 0.000 description 4
- 239000003513 alkali Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- -1 polyazo Polymers 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005755 formation reaction Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- AGIJRRREJXSQJR-UHFFFAOYSA-N 2h-thiazine Chemical compound N1SC=CC=C1 AGIJRRREJXSQJR-UHFFFAOYSA-N 0.000 description 1
- YTZWQUYIRHGHMJ-UHFFFAOYSA-N 3-(1,2-diamino-2-phenylethenyl)benzene-1,2-disulfonic acid Chemical class NC(=C(C1=C(C(=CC=C1)S(=O)(=O)O)S(=O)(=O)O)N)C1=CC=CC=C1 YTZWQUYIRHGHMJ-UHFFFAOYSA-N 0.000 description 1
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 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
- 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
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- GYSSRZJIHXQEHQ-UHFFFAOYSA-N carboxin Chemical compound S1CCOC(C)=C1C(=O)NC1=CC=CC=C1 GYSSRZJIHXQEHQ-UHFFFAOYSA-N 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 150000001844 chromium Chemical class 0.000 description 1
- 150000001868 cobalt Chemical class 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- PPSZHCXTGRHULJ-UHFFFAOYSA-N dioxazine Chemical compound O1ON=CC=C1 PPSZHCXTGRHULJ-UHFFFAOYSA-N 0.000 description 1
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Natural products COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000434 metal complex dye Substances 0.000 description 1
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N o-dicarboxybenzene Natural products OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0071—Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
- C09B67/0072—Preparations with anionic dyes or reactive dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19883842054 DE3842054A1 (de) | 1988-12-14 | 1988-12-14 | Farbstoffpraeparationen |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19883842054 DE3842054A1 (de) | 1988-12-14 | 1988-12-14 | Farbstoffpraeparationen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE3842054A1 DE3842054A1 (de) | 1990-06-21 |
| DE3842054C2 true DE3842054C2 (enrdf_load_stackoverflow) | 1992-06-17 |
Family
ID=6369130
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19883842054 Granted DE3842054A1 (de) | 1988-12-14 | 1988-12-14 | Farbstoffpraeparationen |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE3842054A1 (enrdf_load_stackoverflow) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4008262A1 (de) * | 1990-03-15 | 1991-09-19 | Bayer Ag | Verfahren zur herstellung lagerstabiler farbstoffloesungen |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3342432A1 (de) * | 1983-11-24 | 1985-06-05 | Hoechst Ag, 6230 Frankfurt | Fluessige reaktivfarbstoffzubereitungen und ihre verwendung |
| JPH0781091B2 (ja) * | 1986-02-27 | 1995-08-30 | 住友化学工業株式会社 | 反応染料の液状水性組成物 |
-
1988
- 1988-12-14 DE DE19883842054 patent/DE3842054A1/de active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| DE3842054A1 (de) | 1990-06-21 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0277529B1 (de) | Mischungen von Monoazofarbstoffen | |
| DE2135468A1 (de) | Pigmentzusammensetzungen | |
| DE60008419T2 (de) | Farbstoffpräparate, deren herstellung und deren verwendung | |
| DE2527571A1 (de) | Verfahren zur herstellung von gedeckten farbstoffen oder farblacken | |
| DE3342432A1 (de) | Fluessige reaktivfarbstoffzubereitungen und ihre verwendung | |
| EP0028342B1 (de) | Verwendung von veresterten Oxalkylaten als Präparationsmittel für Farbstoffe und entsprechende Farbstoffzubereitungen | |
| EP0064225B1 (de) | Verwendung von veresterten Oxalkylaten als Präparationsmittel für Farbstoffe und entsprechende Farbstoffzubereitungen | |
| EP0034771B1 (de) | Hochkonzentrierte, lagerstabile und wärmebeständige, fliessfähige, wässrige Dispersion von in Wasser schwer- bis unlöslichen Wirksubstanzen, Verfahren zur Herstellung der Dispersion, Verfahren zum Veredeln von Kunststoffen, Papier oder Textilien sowie veredelte Kunststoffe, veredeltes Papier oder veredelte Textilien | |
| DE3842054C2 (enrdf_load_stackoverflow) | ||
| DE3209533C2 (enrdf_load_stackoverflow) | ||
| DE3689014T2 (de) | Wässrige flüssige Reaktivfarbstoffzusammensetzung. | |
| EP0124866B1 (de) | Kaltwasserdispergierbare Farbstoffgranulate | |
| DE2540739C2 (de) | Verfahren zur Umwandlung eines Küpenfärbematerials in eine Pigmentform | |
| EP0524520B1 (de) | Flüssige Farbstoffzubereitungen | |
| EP0022489A1 (de) | Pulverförmige Farbstoffzubereitung | |
| EP0013576A1 (de) | Verwendung oxalkylierter Novolakharze als Präparationsmittel für Dispersionsfarbstoffe und damit hergestellte Zubereitungen | |
| CH640559A5 (de) | Verfahren zur herstellung von in wasser dispergierbaren pulverfoermigen zubereitungen von dispersionsfarbstoffen. | |
| EP0013919B1 (de) | Wässrige Farbstoffzubereitung und Verfahren zu ihrer Herstellung und ihre Verwendung zum Färben und Bedrucken | |
| EP0097291B1 (de) | Farbstoffpräparationen | |
| EP0152005A2 (de) | Mischungen von Monoazofarbstoffen | |
| DE4026747A1 (de) | Mischungen von monoazofarbstoffen | |
| EP0081737B1 (de) | Flüssigkristalline Phase eines Azoreaktivfarbstoffs und deren Verwendung zum Färben und Bedrucken von natürlichen und synthetischen Substraten | |
| DE2110999C3 (de) | Verfahren zur Herstellung von Kupferphthalocyanin-Pigmenten | |
| DE523910C (de) | Verfahren zur Erhaltung der feinen Verteilung von unloeslichen oder schwer loeslichen Farbstoffen | |
| DE1769252C (de) | Staubarme, pulverförmige Präparate von organischen Farbstoffen |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8110 | Request for examination paragraph 44 | ||
| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition | ||
| 8339 | Ceased/non-payment of the annual fee |