DE1619358A1 - Process for converting crude polyhalocopper phthalocyanines into a pigment form - Google Patents
Process for converting crude polyhalocopper phthalocyanines into a pigment formInfo
- Publication number
- DE1619358A1 DE1619358A1 DE19671619358 DE1619358A DE1619358A1 DE 1619358 A1 DE1619358 A1 DE 1619358A1 DE 19671619358 DE19671619358 DE 19671619358 DE 1619358 A DE1619358 A DE 1619358A DE 1619358 A1 DE1619358 A1 DE 1619358A1
- Authority
- DE
- Germany
- Prior art keywords
- phthalocyanines
- polyhalocopper
- sulfuric acid
- dye
- crude
- 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.)
- Pending
Links
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
- C09B67/0032—Treatment of phthalocyanine pigments
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Description
Verfahren zur Umwandlung von rohen Polyhalogenkupferphthalocyaninen in eine Pigmentform 2. Zusatz zu Patent , ... ... (Patentanmeldung B 83 947 IVc/8m) Gegenstand der Patents . ... ... (Patentanmeldung B 83 ]47 IVc/vm) ist ein Verfahren zur Umwandlung roher Polyhalogenkupferphthalocyanine in hochwertige Pigmente, bei dem man den Rohfarbstoff mit Schwefelsäure und einer organischen Flüssigkeit in Gegenwart von 0,2 bis 2, vorzugsweise 0,5 bis 1,5 Gewichtsteilen Nitrosylschwefelsäure, bezogen auf 1 Gewichtsteil Farbstoff, behandelt.Process for converting crude polyhalogen copper phthalocyanines into a pigment form 2. Addition to patent, ... ... (Patent application B 83 947 IVc / 8m) Subject matter of the patents. ... ... (patent application B 83 ] 47 IVc / vm) is a process for converting crude polyhalogen copper phthalocyanines into high-quality pigments, in which the crude dye is treated with sulfuric acid and an organic liquid in the presence of 0.2 to 2, preferably 5 to 1.5 parts by weight of nitrosylsulfuric acid, based on 1 part by weight of dye, treated.
Es wurde nun gefunden, daß man rohe Polyhalogenkupferphthalocyanine ebenfalls auf vorteilhafte Weise in Pigmente umwandeln kann, wenn man den Rohfarbstoff mit Schwefelsäure und einer organischen Flüs-. sigkeit in Gegenwart von 0;1 his 0,2 Gewichtsteilen Nitrosylschwefelsäure, bezogen auf 1 Gewichtsteil Farbstoff, behandelt.It has now been found that crude polyhalocopper phthalocyanines can also be converted into pigments in an advantageous manner if you use the raw dye with sulfuric acid and an organic hydrofluoric. sigkeit in the presence of 0; 1 his 0.2 part by weight of nitrosylsulfuric acid, based on 1 part by weight of dye, treated.
Fär das Verfahren dieses Zusatzpatents gelten im übrigen die Angaben des Hauptpatents.For the procedure of this additional patent, the information applies of the main patent.
Beispiel 20 Teile (hier wie im folgenden Gewichtsteile) Hexadecachlorkupferphtrialocyanin werden in 200 Teilen Trichlorbenzol suspendiert und auf 110 °C erwärmt. Im Verlauf von ungefähr 30 Minuten läßt man bei guter Rührung eine Mischung von 25 Teilen konzentrierter Schwefelsäure und 3 Teilen Nitrosylschwefelsäure zulaufen und hält die Mischung noch eine Stunde bei 110 oC. Man kühlt auf Raumtemperatur, gibt Wasser zu, saugt das Pigment ab und wäscht mit Dimethylformamid und Wasser aus.Example 20 parts (here as in the following parts by weight) of hexadecachlorocopper phtrialocyanine are suspended in 200 parts of trichlorobenzene and to 110 ° C warmed up. Allow to mix for about 30 minutes with good agitation run in from 25 parts of concentrated sulfuric acid and 3 parts of nitrosylsulfuric acid and keep the mixture at 110 oC for another hour. One cools to room temperature, adds water, sucks off the pigment and washes with dimethylformamide and water the end.
Man erhält 18 Teile eines gelbstichigen Grünpigments mit sehr guter Farbstärke und Farbreinheit.18 parts of a yellowish green pigment with very good Color strength and color purity.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US580909A US3370065A (en) | 1965-09-30 | 1966-09-21 | Converting crude polyhalocopper phthalocyanines into a pigment form |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1619358A1 true DE1619358A1 (en) | 1971-05-13 |
Family
ID=24323091
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19671619358 Pending DE1619358A1 (en) | 1966-09-21 | 1967-01-07 | Process for converting crude polyhalocopper phthalocyanines into a pigment form |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE1619358A1 (en) |
-
1967
- 1967-01-07 DE DE19671619358 patent/DE1619358A1/en active Pending
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE1619358A1 (en) | Process for converting crude polyhalocopper phthalocyanines into a pigment form | |
DE1210110B (en) | Process for the preparation of quinacridones | |
DE688908C (en) | Process for the production of sulfur-containing dyes | |
AT166228B (en) | Dye preparations or dye baths, in particular for dyeing cellulose esters. | |
DE536294C (en) | Process for the preparation of Kuepen dyes of the anthraquinone series | |
DE451549C (en) | Process for the preparation of green-coloring, sulphurous cow dyes | |
DE515680C (en) | Process for the preparation of pyrazolanthrone-2-carboxylic acid | |
DE445443C (en) | Process for the production of indigoid dyes | |
DE949942C (en) | Process for the production of a finely distributed Kuepen dye | |
DE518120C (en) | Process for the preparation of 2-aroylpyrazole anthrones | |
DE507832C (en) | Process for the representation of orange-tinted cow dyes | |
DE370155C (en) | Process for the production of Kuepen dyes | |
DE514433C (en) | Process for the production of green dyes of the benzanthrone series | |
DE97541C (en) | ||
DE515096C (en) | Process for the preparation of N-dihydro-1íñ2íñ2íñ1-anthraquinonazine dyes | |
DE461450C (en) | Process for the preparation of condensation products of the anthraquinone series | |
DE628230C (en) | Process for the production of Kuepen dyes | |
DE570968C (en) | Process for the production of a yellow Kuepen dye | |
DE518230C (en) | Process for the preparation of Kuepen dyes of the N-dihydro-1, 2, 2, 1-anthraquinonazine series | |
DE588782C (en) | Process for the preparation of a monoazo dye | |
DE556161C (en) | Process for the preparation of 2-chloroanthraquinone-3-carboxylic acid | |
DE1543619A1 (en) | Process for the preparation of 5-nitro-1,4-dihydroxyantraquinone | |
DE935988C (en) | Process for the production of Kuepen dyes | |
DE909385C (en) | Process for the production of Kuepen dyes | |
DE576466C (en) | Process for the production of new condensation products |