CS232848B1 - Preparation method of blue phthalocyanine pigment beta modification - Google Patents

Preparation method of blue phthalocyanine pigment beta modification Download PDF

Info

Publication number: CS232848B1
Authority: CS; Czechoslovakia
Prior art keywords: beta modification; preparation; glycols; blue phthalocyanine; blue
Prior art date: 1983-05-04

Application number

CS313983A

Other languages

Czech (cs)

English (en)

Inventor

Vladimir A Smrcek

Jan Rakusan

Jan B Ladyzenskyj

Frantisek Stepanek

Valentina N Gorenko

Vladimir Zverina

Arkadij L Poznjakevic

Frantisek Velasovsky

Margarita V Astafjeva

Antonin Novak

Ilja Stepanek

Jan Sebesta

Original Assignee

Smrcek

Jan Rakusan

Jan B Ladyzenskyj

Frantisek Stepanek

Valentina N Gorenko

Vladimir Zverina

Arkadij L Poznjakevic

Frantisek Velasovsky

Margarita V Astafjeva

Antonin Novak

Ilja Stepanek

Jan Sebesta

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.)

1983-05-04

Filing date

1983-05-04

Publication date

1985-02-14

1983-05-04 Application filed by Smrcek, Jan Rakusan, Jan B Ladyzenskyj, Frantisek Stepanek, Valentina N Gorenko, Vladimir Zverina, Arkadij L Poznjakevic, Frantisek Velasovsky, Margarita V Astafjeva, Antonin Novak, Ilja Stepanek, Jan Sebesta filed Critical Smrcek

1983-05-04 Priority to CS313983A priority Critical patent/CS232848B1/cs

1983-08-29 Priority to DD25431983A priority patent/DD243182A3/de

1983-08-31 Priority to SU837773095A priority patent/SU1341178A1/ru

1985-02-14 Publication of CS232848B1 publication Critical patent/CS232848B1/cs

Links

239000000049 pigment Substances 0.000 title claims description 23
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 title claims description 15
230000004048 modification Effects 0.000 title claims description 13
238000012986 modification Methods 0.000 title claims description 13
238000002360 preparation method Methods 0.000 title description 5
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 12
150000002334 glycols Chemical class 0.000 claims description 12
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 9
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 9
229920000151 polyglycol Polymers 0.000 claims description 7
239000010695 polyglycol Substances 0.000 claims description 7
239000011780 sodium chloride Substances 0.000 claims description 6
238000004519 manufacturing process Methods 0.000 claims description 5
239000000203 mixture Substances 0.000 claims description 5
239000011541 reaction mixture Substances 0.000 claims description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
238000000227 grinding Methods 0.000 claims description 3
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 3
238000000034 method Methods 0.000 description 17
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 8
239000002904 solvent Substances 0.000 description 7
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
230000003750 conditioning effect Effects 0.000 description 4
239000000976 ink Substances 0.000 description 4
239000003960 organic solvent Substances 0.000 description 4
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
239000006185 dispersion Substances 0.000 description 3
231100000331 toxic Toxicity 0.000 description 3
230000002588 toxic effect Effects 0.000 description 3
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
239000000975 dye Substances 0.000 description 2
238000005516 engineering process Methods 0.000 description 2
LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
239000003973 paint Substances 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
235000005956 Cosmos caudatus Nutrition 0.000 description 1
244000293323 Cosmos caudatus Species 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
239000002202 Polyethylene glycol Substances 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
150000001335 aliphatic alkanes Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
150000004996 alkyl benzenes Chemical class 0.000 description 1
DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
150000004982 aromatic amines Chemical class 0.000 description 1
239000003849 aromatic solvent Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000008280 blood Substances 0.000 description 1
210000004369 blood Anatomy 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
-1 chlorine ions Chemical class 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
238000004821 distillation Methods 0.000 description 1
231100000086 high toxicity Toxicity 0.000 description 1
229910017053 inorganic salt Inorganic materials 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000002574 poison Substances 0.000 description 1
231100000614 poison Toxicity 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
239000000047 product Substances 0.000 description 1
230000008929 regeneration Effects 0.000 description 1
238000011069 regeneration method Methods 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
238000001256 steam distillation Methods 0.000 description 1
239000000725 suspension Substances 0.000 description 1
229950011008 tetrachloroethylene Drugs 0.000 description 1
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
231100000925 very toxic Toxicity 0.000 description 1
239000002351 wastewater Substances 0.000 description 1

Landscapes

Inks, Pencil-Leads, Or Crayons (AREA)
Management, Administration, Business Operations System, And Electronic Commerce (AREA)
Pigments, Carbon Blacks, Or Wood Stains (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)

CS313983A 1983-05-04 1983-05-04 Preparation method of blue phthalocyanine pigment beta modification CS232848B1 (en)

Priority Applications (3)

Application Number	Priority Date	Filing Date	Title
CS313983A CS232848B1 (en)	1983-05-04	1983-05-04	Preparation method of blue phthalocyanine pigment beta modification
DD25431983A DD243182A3 (de)	1983-05-04	1983-08-29	Verfahren zur herstellung der beta-modifikation bon blauen phthalocyaninpigmenten
SU837773095A SU1341178A1 (ru)	1983-05-04	1983-08-31	Способ получени голубых фталоцианиновых пигментов @ -модификации

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CS313983A CS232848B1 (en)	1983-05-04	1983-05-04	Preparation method of blue phthalocyanine pigment beta modification

Publications (1)

Publication Number	Publication Date
CS232848B1 true CS232848B1 (en)	1985-02-14

Family

ID=5370586

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS313983A CS232848B1 (en)	1983-05-04	1983-05-04	Preparation method of blue phthalocyanine pigment beta modification

Country Status (3)

Country	Link
CS (1)	CS232848B1 (de)
DD (1)	DD243182A3 (de)
SU (1)	SU1341178A1 (de)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3922734A1 (de) *	1989-07-11	1991-01-24	Basf Ag	Verfahren zur herstellung von farbstarken, transparenten und leicht dispergierbaren kupferphthalocyaninpigmenten der ss-modifikation
GB9326374D0 (en) *	1993-12-23	1994-02-23	Zeneca Ltd	Process
RU2265024C1 (ru) *	2004-05-20	2005-11-27	Оао "Компания Славич"	Способ получения титанилфталоцианина

1983
- 1983-05-04 CS CS313983A patent/CS232848B1/cs unknown
- 1983-08-29 DD DD25431983A patent/DD243182A3/de not_active IP Right Cessation
- 1983-08-31 SU SU837773095A patent/SU1341178A1/ru active

Also Published As

Publication number	Publication date
SU1341178A1 (ru)	1987-09-30
DD243182A3 (de)	1987-02-25

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DE2135468A1 (de)	1972-02-24	Pigmentzusammensetzungen
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JP5578727B2 (ja)	2014-08-27	ジオキサジンベースの顔料調合物
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DE3641891C2 (de)	1999-01-14	Verfahren zur Herstellung von Dimethylaminomethyl-Kupferphthalocyanin und/oder seinen Derivaten
JPS63248864A (ja)	1988-10-17	易分散性銅フタロシアニン顔料組成物及びその製造方法
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EP1038923B1 (de)	2005-06-22	Verfahren zur Herstellung von Dioxazin-Verbindungen
US3865605A (en)	1975-02-11	Readily dispersible pigments
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