IE43273B1 - Pigmentary -copper phthalocyanine - Google Patents

Pigmentary -copper phthalocyanine

Info

Publication number: IE43273B1
Authority: IE; Ireland
Prior art keywords: pigment; copper phthalocyanine; milling; mixture; process according
Prior art date: 1975-05-02

Application number

IE937/76A

Other languages

English (en)

Other versions

IE43273L (en

Original Assignee

Du Pont

Priority date (The priority date 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 date listed.)

1975-05-02

Filing date

1976-04-30

Publication date

1981-01-28

1976-04-30 Application filed by Du Pont filed Critical Du Pont

1976-11-02 Publication of IE43273L publication Critical patent/IE43273L/xx

1981-01-28 Publication of IE43273B1 publication Critical patent/IE43273B1/en

Links

238000003801 milling Methods 0.000 claims abstract description 50
239000000049 pigment Substances 0.000 claims abstract description 44
239000003795 chemical substances by application Substances 0.000 claims abstract description 38
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 abstract description 37
239000000203 mixture Substances 0.000 claims abstract description 32
230000003750 conditioning effect Effects 0.000 claims abstract description 31
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 23
150000003839 salts Chemical class 0.000 claims abstract description 20
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims abstract description 15
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract description 13
229920005862 polyol Polymers 0.000 claims abstract description 13
150000003077 polyols Chemical class 0.000 claims abstract description 13
239000002002 slurry Substances 0.000 claims abstract description 9
230000000694 effects Effects 0.000 claims abstract description 5
150000002148 esters Chemical class 0.000 claims abstract description 5
238000001914 filtration Methods 0.000 claims abstract description 4
238000005406 washing Methods 0.000 claims abstract description 4
238000010438 heat treatment Methods 0.000 claims abstract 2
238000000034 method Methods 0.000 claims description 33
230000008569 process Effects 0.000 claims description 18
229910021578 Iron(III) chloride Inorganic materials 0.000 claims description 6
239000002253 acid Substances 0.000 claims description 6
RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 claims description 6
238000004519 manufacturing process Methods 0.000 claims description 5
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 3
239000007864 aqueous solution Substances 0.000 claims description 3
150000001875 compounds Chemical class 0.000 claims description 2
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims 5
229910052802 copper Inorganic materials 0.000 claims 5
239000010949 copper Substances 0.000 claims 5
239000011260 aqueous acid Substances 0.000 abstract description 3
150000002170 ethers Chemical class 0.000 abstract description 3
238000000227 grinding Methods 0.000 description 15
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 14
239000007788 liquid Substances 0.000 description 10
JVTCNOASZYIKTG-UHFFFAOYSA-N stk329495 Chemical compound [Cu].[N-]1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)[N-]3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 JVTCNOASZYIKTG-UHFFFAOYSA-N 0.000 description 8
239000011780 sodium chloride Substances 0.000 description 7
239000007787 solid Substances 0.000 description 7
238000002156 mixing Methods 0.000 description 5
QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid group Chemical class S(O)(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
230000009471 action Effects 0.000 description 4
230000001143 conditioned effect Effects 0.000 description 4
239000002245 particle Substances 0.000 description 4
239000000047 product Substances 0.000 description 4
238000010008 shearing Methods 0.000 description 4
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
239000006185 dispersion Substances 0.000 description 3
238000000605 extraction Methods 0.000 description 3
239000001257 hydrogen Substances 0.000 description 3
229910052739 hydrogen Inorganic materials 0.000 description 3
125000004435 hydrogen atom Chemical class [H]* 0.000 description 3
229910017053 inorganic salt Inorganic materials 0.000 description 3
235000011837 pasties Nutrition 0.000 description 3
229920001223 polyethylene glycol Polymers 0.000 description 3
238000000926 separation method Methods 0.000 description 3
239000002904 solvent Substances 0.000 description 3
SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
239000002202 Polyethylene glycol Substances 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
238000009835 boiling Methods 0.000 description 2
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
239000012065 filter cake Substances 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
239000003973 paint Substances 0.000 description 2
ZWVMLYRJXORSEP-UHFFFAOYSA-N 1,2,6-Hexanetriol Chemical compound OCCCCC(O)CO ZWVMLYRJXORSEP-UHFFFAOYSA-N 0.000 description 1
AGYUOJIYYGGHKV-UHFFFAOYSA-N 1,2-bis(2-chloroethoxy)ethane Chemical compound ClCCOCCOCCCl AGYUOJIYYGGHKV-UHFFFAOYSA-N 0.000 description 1
229940043375 1,5-pentanediol Drugs 0.000 description 1
DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical class CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
RRQYJINTUHWNHW-UHFFFAOYSA-N 1-ethoxy-2-(2-ethoxyethoxy)ethane Chemical compound CCOCCOCCOCC RRQYJINTUHWNHW-UHFFFAOYSA-N 0.000 description 1
ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 1
FPZWZCWUIYYYBU-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl acetate Chemical compound CCOCCOCCOC(C)=O FPZWZCWUIYYYBU-UHFFFAOYSA-N 0.000 description 1
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 description 1
SDHQGBWMLCBNSM-UHFFFAOYSA-N 2-[2-(2-methoxyethoxy)ethoxy]ethyl acetate Chemical compound COCCOCCOCCOC(C)=O SDHQGBWMLCBNSM-UHFFFAOYSA-N 0.000 description 1
WAEVWDZKMBQDEJ-UHFFFAOYSA-N 2-[2-(2-methoxypropoxy)propoxy]propan-1-ol Chemical class COC(C)COC(C)COC(C)CO WAEVWDZKMBQDEJ-UHFFFAOYSA-N 0.000 description 1
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical class COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
239000004606 Fillers/Extenders Substances 0.000 description 1
QVHMSMOUDQXMRS-UHFFFAOYSA-N PPG n4 Chemical compound CC(O)COC(C)COC(C)COC(C)CO QVHMSMOUDQXMRS-UHFFFAOYSA-N 0.000 description 1
ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000002411 adverse Effects 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
238000000498 ball milling Methods 0.000 description 1
TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 1
230000008901 benefit Effects 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
150000001805 chlorine compounds Chemical class 0.000 description 1
239000003086 colorant Substances 0.000 description 1
VVOLVFOSOPJKED-UHFFFAOYSA-N copper phthalocyanine Chemical compound [Cu].N=1C2=NC(C3=CC=CC=C33)=NC3=NC(C3=CC=CC=C33)=NC3=NC(C3=CC=CC=C33)=NC3=NC=1C1=CC=CC=C12 VVOLVFOSOPJKED-UHFFFAOYSA-N 0.000 description 1
239000013078 crystal Substances 0.000 description 1
238000010908 decantation Methods 0.000 description 1
229940019778 diethylene glycol diethyl ether Drugs 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000010494 dissociation reaction Methods 0.000 description 1
230000005593 dissociations Effects 0.000 description 1
238000009837 dry grinding Methods 0.000 description 1
238000001035 drying Methods 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
230000001747 exhibiting effect Effects 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
239000008187 granular material Substances 0.000 description 1
229940051250 hexylene glycol Drugs 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
230000006872 improvement Effects 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
239000000976 ink Substances 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
238000010297 mechanical methods and process Methods 0.000 description 1
230000005226 mechanical processes and functions Effects 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000011707 mineral Substances 0.000 description 1
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
238000006053 organic reaction Methods 0.000 description 1
229920001515 polyalkylene glycol Polymers 0.000 description 1
-1 polybutylene Polymers 0.000 description 1
229920001748 polybutylene Polymers 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
230000001376 precipitating effect Effects 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
238000011084 recovery Methods 0.000 description 1
239000005060 rubber Substances 0.000 description 1
238000005549 size reduction Methods 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
239000002966 varnish 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
- C09B67/0025—Crystal modifications; Special X-ray patterns
- C09B67/0026—Crystal modifications; Special X-ray patterns of phthalocyanine pigments
- 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
- C09B67/0001—Post-treatment of organic pigments or dyes
- C09B67/0022—Wet grinding of pigments
- C09B67/0023—Wet grinding of pigments of phthalocyanines

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Chemistry (AREA)
Pigments, Carbon Blacks, Or Wood Stains (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)

IE937/76A 1975-05-02 1976-04-30 Pigmentary -copper phthalocyanine IE43273B1 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US05/573,993 US3954795A (en)	1975-05-02	1975-05-02	Process for preparing pigmentary β-copper phthalocyanine

Publications (2)

Publication Number	Publication Date
IE43273L IE43273L (en)	1976-11-02
IE43273B1 true IE43273B1 (en)	1981-01-28

Family

ID=24294245

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IE937/76A IE43273B1 (en)	1975-05-02	1976-04-30	Pigmentary -copper phthalocyanine

Country Status (12)

Country	Link
US (1)	US3954795A (2)
JP (1)	JPS51134722A (2)
BE (1)	BE841380A (2)
CH (1)	CH601439A5 (2)
DE (1)	DE2619326A1 (2)
DK (1)	DK194276A (2)
FR (1)	FR2309610A1 (2)
GB (1)	GB1490945A (2)
IE (1)	IE43273B1 (2)
IT (1)	IT1062099B (2)
LU (1)	LU74865A1 (2)
NL (1)	NL7604602A (2)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5229508A (en) *	1987-12-17	1993-07-20	Toyo Ink Manufacturing Co., Inc.	Process for the preparation of copper phthalocyanine pigment
KR100204380B1 (ko) *	1995-01-27	1999-06-15	나가시마 므쓰오	잉크젯 기록용액 및 그 제조방법
JP2005002250A (ja) *	2003-06-13	2005-01-06	Toyo Ink Mfg Co Ltd	β型銅フタロシアニン顔料の製造方法
US7255733B2 (en) *	2003-06-20	2007-08-14	Toyo Ink Mfg. Co., Ltd.	Process for the production of β type copper phthalocyanine pigment and a use thereof
DE102008006859A1 (de) *	2008-01-31	2009-08-06	Clariant International Limited	Verfahren zur Konditionierung von Carbonsäureestergruppen-haltigen Azopigmenten
JP5708028B2 (ja) *	2011-02-25	2015-04-30	東洋インキＳｃホールディングス株式会社	カラーフィルタ用着色組成物、及びカラーフィルタ

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2833783A (en) *	1954-04-12	1958-05-06	Du Pont	Treatment of polychloro copper phthalocyanine
US2982666A (en) *	1958-12-08	1961-05-02	California Ink Company Inc	Method of conditioning organic pigments and resultant product

1975
- 1975-05-02 US US05/573,993 patent/US3954795A/en not_active Expired - Lifetime
1976
- 1976-04-28 GB GB17259/76A patent/GB1490945A/en not_active Expired
- 1976-04-29 IT IT22815/76A patent/IT1062099B/it active
- 1976-04-29 FR FR7612736A patent/FR2309610A1/fr active Granted
- 1976-04-29 NL NL7604602A patent/NL7604602A/xx not_active Application Discontinuation
- 1976-04-30 JP JP51048660A patent/JPS51134722A/ja active Pending
- 1976-04-30 LU LU74865A patent/LU74865A1/xx unknown
- 1976-04-30 DK DK194276A patent/DK194276A/da unknown
- 1976-04-30 CH CH545576A patent/CH601439A5/xx not_active IP Right Cessation
- 1976-04-30 BE BE166660A patent/BE841380A/xx unknown
- 1976-04-30 DE DE19762619326 patent/DE2619326A1/de not_active Withdrawn
- 1976-04-30 IE IE937/76A patent/IE43273B1/en unknown

Also Published As

Publication number	Publication date
LU74865A1 (2)	1977-02-08
BE841380A (fr)	1976-11-03
IT1062099B (it)	1983-06-25
CH601439A5 (2)	1978-07-14
JPS51134722A (en)	1976-11-22
DE2619326A1 (de)	1976-11-11
GB1490945A (en)	1977-11-02
NL7604602A (nl)	1976-11-04
FR2309610B1 (2)	1980-01-11
FR2309610A1 (fr)	1976-11-26
US3954795A (en)	1976-05-04
DK194276A (da)	1976-11-03
IE43273L (en)	1976-11-02

Publication	Publication Date	Title
US2982666A (en)	1961-05-02	Method of conditioning organic pigments and resultant product
KR100255973B1 (ko)	2000-05-01	알파-상의 구리 프탈로시아닌 안료제제의 제조방법
JPH0376877A (ja)	1991-04-02	ペリレン‐３，４，９，１０‐テトラカルボン酸ジイミド系顔料の使用方法
AU658958B2 (en)	1995-05-04	Pigment composition
US3954795A (en)	1976-05-04	Process for preparing pigmentary β-copper phthalocyanine
JPH02294365A (ja)	1990-12-05	ペースト状の高粘度印刷インキに適した銅フタロシアニンの製造方法、およびペースト状印刷インキの製造方法
EP0655485B1 (de)	1999-12-29	Verfahren zur Herstellung von linearen, unsubstituierten Chinacridonpigmenten der beta-Phasen
US3936315A (en)	1976-02-03	Conversion of crude phthalocyanines into pigments
JPH0220663B2 (2)	1990-05-10
US4694078A (en)	1987-09-15	Production of pigmentary copper phthalocyanine
JPS6143390B2 (2)	1986-09-27
WO1981003624A1 (en)	1981-12-24	Process for salt grinding of pigments
JP2000273345A (ja)	2000-10-03	アゾレーキ顔料組成物
US3951678A (en)	1976-04-20	Pigmentation of crude metal phthalocyanines
US2645643A (en)	1953-07-14	Process for producing phthalocyanine coloring matters
US3748164A (en)	1973-07-24	Novel pigmentation method for organic pigments
US3963743A (en)	1976-06-15	Method of conditioning phthalocyanine pigments and product thereof
US3536502A (en)	1970-10-27	Copper phthalocyanine pigment compositions
JP2006328262A (ja)	2006-12-07	微細キナクリドン顔料の製造方法
US7115164B2 (en)	2006-10-03	Preparation of yellow pigments
JPS6361348B2 (2)	1988-11-29
US3647494A (en)	1972-03-07	Process for making solid solutions of quinacridone and derivatives thereof
JPH04320458A (ja)	1992-11-11	銅フタロシアニン顔料の製造方法
DE1619618B2 (de)	1973-03-08	Chinacridon-pigmentmasse
CA1052058A (en)	1979-04-10	Pigmentation of crude metal phthalocyanines