DE2403706A1 - Verfahren zur herstellung von chlorierten kupferphthalocyaninen - Google Patents
Verfahren zur herstellung von chlorierten kupferphthalocyaninenInfo
- Publication number
- DE2403706A1 DE2403706A1 DE2403706A DE2403706A DE2403706A1 DE 2403706 A1 DE2403706 A1 DE 2403706A1 DE 2403706 A DE2403706 A DE 2403706A DE 2403706 A DE2403706 A DE 2403706A DE 2403706 A1 DE2403706 A1 DE 2403706A1
- Authority
- DE
- Germany
- Prior art keywords
- chlorine
- copper phthalocyanine
- chlorination
- chlorinated
- content
- 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.)
- Withdrawn
Links
- 238000000034 method Methods 0.000 title claims description 30
- 238000004519 manufacturing process Methods 0.000 title description 8
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical class [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 title description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 48
- 239000000460 chlorine Substances 0.000 claims description 47
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 46
- 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 claims description 43
- 238000005660 chlorination reaction Methods 0.000 claims description 23
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 9
- 229910052740 iodine Inorganic materials 0.000 claims description 9
- 239000011630 iodine Substances 0.000 claims description 9
- 150000001879 copper Chemical class 0.000 claims description 7
- 239000011593 sulfur Substances 0.000 claims description 7
- 229910052717 sulfur Inorganic materials 0.000 claims description 7
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 6
- 230000000694 effects Effects 0.000 claims description 6
- 239000003973 paint Substances 0.000 claims description 5
- 238000004040 coloring Methods 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 3
- 239000000976 ink Substances 0.000 claims description 2
- 239000004922 lacquer Substances 0.000 claims description 2
- 230000000485 pigmenting effect Effects 0.000 claims description 2
- 229920000642 polymer Polymers 0.000 claims 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 37
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 11
- 239000003054 catalyst Substances 0.000 description 11
- 239000000049 pigment Substances 0.000 description 10
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000012065 filter cake Substances 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 241000974482 Aricia saepiolus Species 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 238000000227 grinding Methods 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- 238000004821 distillation Methods 0.000 description 3
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 210000003298 dental enamel Anatomy 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 230000008929 regeneration Effects 0.000 description 2
- 238000011069 regeneration method Methods 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 description 1
- 241000282376 Panthera tigris Species 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001804 chlorine Chemical class 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- XTHPWXDJESJLNJ-UHFFFAOYSA-N chlorosulfonic acid Substances OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- -1 copper phthalocyanine sulfonic acids Chemical class 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000005189 flocculation Methods 0.000 description 1
- 230000016615 flocculation Effects 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 231100000989 no adverse effect Toxicity 0.000 description 1
- 238000006864 oxidative decomposition reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 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
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000011044 quartzite Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 230000019635 sulfation Effects 0.000 description 1
- 238000005670 sulfation reaction Methods 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 150000003463 sulfur Chemical class 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 230000035899 viability Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002699 waste material Substances 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
- C09B47/00—Porphines; Azaporphines
- C09B47/04—Phthalocyanines abbreviation: Pc
- C09B47/08—Preparation from other phthalocyanine compounds, e.g. cobaltphthalocyanineamine complex
- C09B47/10—Obtaining compounds having halogen atoms directly bound to the phthalocyanine skeleton
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Priority Applications (12)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2403706A DE2403706A1 (de) | 1974-01-26 | 1974-01-26 | Verfahren zur herstellung von chlorierten kupferphthalocyaninen |
IN2870/CAL/74A IN141183B (enrdf_load_stackoverflow) | 1974-01-26 | 1974-12-27 | |
CH79575A CH606327A5 (enrdf_load_stackoverflow) | 1974-01-26 | 1975-01-23 | |
IT19578/75A IT1031144B (it) | 1974-01-26 | 1975-01-24 | Processo per la preparazione di cuprofta ocianine clorura te |
BR510/75A BR7500510A (pt) | 1974-01-26 | 1975-01-24 | Processo para a preparacao de ftalocianinas de cobre cloradas e aplicacao das mesmas |
DK23175A DK139756C (da) | 1974-01-26 | 1975-01-24 | Fremgangsmaade til fremstilling af chlorerede kobberphthalocyaniner |
JP50009905A JPS5850264B2 (ja) | 1974-01-26 | 1975-01-24 | 塩素化した銅フタロシアニン化合物の製法 |
CA218,650A CA1028693A (en) | 1974-01-26 | 1975-01-24 | Process for the preparation of chlorinated copper phthalocyanines |
AR257410A AR202336A1 (es) | 1974-01-26 | 1975-01-24 | Procedimiento para fabricar ftalocianinas de cobre en oleum |
GB3255/75A GB1495442A (en) | 1974-01-26 | 1975-01-24 | Process for preparing chlorinated copper phthalocyanines |
BE152736A BE824816A (fr) | 1974-01-26 | 1975-01-27 | Procede de preparation de phtalocyanines de cuivre chlorees |
FR7502387A FR2259142B1 (enrdf_load_stackoverflow) | 1974-01-26 | 1975-01-27 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2403706A DE2403706A1 (de) | 1974-01-26 | 1974-01-26 | Verfahren zur herstellung von chlorierten kupferphthalocyaninen |
Publications (1)
Publication Number | Publication Date |
---|---|
DE2403706A1 true DE2403706A1 (de) | 1975-08-14 |
Family
ID=5905736
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE2403706A Withdrawn DE2403706A1 (de) | 1974-01-26 | 1974-01-26 | Verfahren zur herstellung von chlorierten kupferphthalocyaninen |
Country Status (12)
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5028801B2 (ja) | 2004-01-13 | 2012-09-19 | 旭硝子株式会社 | 含フッ素ポリエーテル化合物 |
-
1974
- 1974-01-26 DE DE2403706A patent/DE2403706A1/de not_active Withdrawn
- 1974-12-27 IN IN2870/CAL/74A patent/IN141183B/en unknown
-
1975
- 1975-01-23 CH CH79575A patent/CH606327A5/xx not_active IP Right Cessation
- 1975-01-24 AR AR257410A patent/AR202336A1/es active
- 1975-01-24 DK DK23175A patent/DK139756C/da not_active IP Right Cessation
- 1975-01-24 CA CA218,650A patent/CA1028693A/en not_active Expired
- 1975-01-24 GB GB3255/75A patent/GB1495442A/en not_active Expired
- 1975-01-24 JP JP50009905A patent/JPS5850264B2/ja not_active Expired
- 1975-01-24 BR BR510/75A patent/BR7500510A/pt unknown
- 1975-01-24 IT IT19578/75A patent/IT1031144B/it active
- 1975-01-27 BE BE152736A patent/BE824816A/xx unknown
- 1975-01-27 FR FR7502387A patent/FR2259142B1/fr not_active Expired
Also Published As
Publication number | Publication date |
---|---|
FR2259142B1 (enrdf_load_stackoverflow) | 1979-08-03 |
CH606327A5 (enrdf_load_stackoverflow) | 1978-10-31 |
AR202336A1 (es) | 1975-05-30 |
BR7500510A (pt) | 1975-11-11 |
IT1031144B (it) | 1979-04-30 |
JPS50104229A (enrdf_load_stackoverflow) | 1975-08-18 |
DK23175A (enrdf_load_stackoverflow) | 1975-09-22 |
DK139756C (da) | 1979-09-17 |
GB1495442A (en) | 1977-12-21 |
BE824816A (fr) | 1975-07-28 |
DK139756B (da) | 1979-04-09 |
JPS5850264B2 (ja) | 1983-11-09 |
IN141183B (enrdf_load_stackoverflow) | 1977-01-29 |
CA1028693A (en) | 1978-03-28 |
FR2259142A1 (enrdf_load_stackoverflow) | 1975-08-22 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
OD | Request for examination | ||
8130 | Withdrawal |