DD207382A5 - Verfahren zur herstellung von pigment- bzw. farbstoffpraeparaten - Google Patents

Verfahren zur herstellung von pigment- bzw. farbstoffpraeparaten Download PDF

Info

Publication number: DD207382A5
Authority: DD; German Democratic Republic
Prior art keywords: polyamide; alcohol; parts; preparation; pigment
Prior art date: 1981-12-23

Application number

DD24632382A

Other languages

German (de)

English (en)

Inventor

Guenther Zwahlen

Original Assignee

Ciba Geigy Ag

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.)

1981-12-23

Filing date

1982-12-21

Publication date

1984-02-29

1982-12-21 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1984-02-29 Publication of DD207382A5 publication Critical patent/DD207382A5/de

Links

239000000049 pigment Substances 0.000 title claims abstract description 38
238000004519 manufacturing process Methods 0.000 title abstract description 3
238000002360 preparation method Methods 0.000 claims abstract description 58
239000004952 Polyamide Substances 0.000 claims abstract description 48
229920002647 polyamide Polymers 0.000 claims abstract description 48
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims abstract description 33
238000000034 method Methods 0.000 claims abstract description 33
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 28
239000002904 solvent Substances 0.000 claims abstract description 16
238000004898 kneading Methods 0.000 claims abstract description 15
229910017053 inorganic salt Inorganic materials 0.000 claims abstract description 7
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims abstract description 6
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 6
VGTPCRGMBIAPIM-UHFFFAOYSA-M sodium thiocyanate Chemical compound [Na+].[S-]C#N VGTPCRGMBIAPIM-UHFFFAOYSA-M 0.000 claims abstract description 5
UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 claims abstract description 4
239000001110 calcium chloride Substances 0.000 claims abstract description 4
229910001628 calcium chloride Inorganic materials 0.000 claims abstract description 4
DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims abstract 2
101000588924 Anthopleura elegantissima Delta-actitoxin-Ael1a Proteins 0.000 claims description 7
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 6
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 claims description 6
JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 claims description 4
235000011037 adipic acid Nutrition 0.000 claims description 3
239000001361 adipic acid Substances 0.000 claims description 3
239000003513 alkali Substances 0.000 claims description 2
BTLSLHNLDQCWKS-UHFFFAOYSA-N oxocan-2-one Chemical compound O=C1CCCCCCO1 BTLSLHNLDQCWKS-UHFFFAOYSA-N 0.000 claims 1
150000003839 salts Chemical class 0.000 abstract description 19
150000004820 halides Chemical class 0.000 abstract description 2
239000011347 resin Substances 0.000 abstract description 2
229920005989 resin Polymers 0.000 abstract description 2
229910052783 alkali metal Inorganic materials 0.000 abstract 1
150000001340 alkali metals Chemical class 0.000 abstract 1
238000010186 staining Methods 0.000 abstract 1
229920002292 Nylon 6 Polymers 0.000 description 23
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 19
239000000243 solution Substances 0.000 description 18
239000000975 dye Substances 0.000 description 17
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 12
239000008187 granular material Substances 0.000 description 10
235000013339 cereals Nutrition 0.000 description 9
-1 aliphatic alcohols Chemical class 0.000 description 7
239000000835 fiber Substances 0.000 description 7
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
150000001298 alcohols Chemical class 0.000 description 6
239000000203 mixture Substances 0.000 description 6
239000011780 sodium chloride Substances 0.000 description 6
238000000227 grinding Methods 0.000 description 5
229910052751 metal Inorganic materials 0.000 description 5
239000002184 metal Substances 0.000 description 5
239000000843 powder Substances 0.000 description 5
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
238000001816 cooling Methods 0.000 description 4
238000009826 distribution Methods 0.000 description 4
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
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 4
MSXVEPNJUHWQHW-UHFFFAOYSA-N 2-methylbutan-2-ol Chemical compound CCC(C)(C)O MSXVEPNJUHWQHW-UHFFFAOYSA-N 0.000 description 3
229920002302 Nylon 6,6 Polymers 0.000 description 3
239000004927 clay Substances 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
239000000463 material Substances 0.000 description 3
238000010992 reflux Methods 0.000 description 3
239000000725 suspension Substances 0.000 description 3
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 2
239000006229 carbon black Substances 0.000 description 2
229910052804 chromium Inorganic materials 0.000 description 2
239000011651 chromium Substances 0.000 description 2
230000001419 dependent effect Effects 0.000 description 2
238000001125 extrusion Methods 0.000 description 2
239000012065 filter cake Substances 0.000 description 2
235000019253 formic acid Nutrition 0.000 description 2
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 description 2
ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
235000019239 indanthrene blue RS Nutrition 0.000 description 2
UHOKSCJSTAHBSO-UHFFFAOYSA-N indanthrone blue Chemical compound C1=CC=C2C(=O)C3=CC=C4NC5=C6C(=O)C7=CC=CC=C7C(=O)C6=CC=C5NC4=C3C(=O)C2=C1 UHOKSCJSTAHBSO-UHFFFAOYSA-N 0.000 description 2
238000002347 injection Methods 0.000 description 2
239000007924 injection Substances 0.000 description 2
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
239000002245 particle Substances 0.000 description 2
239000000047 product Substances 0.000 description 2
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
239000000126 substance Substances 0.000 description 2
229920000571 Nylon 11 Polymers 0.000 description 1
229920000299 Nylon 12 Polymers 0.000 description 1
NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
RHQDFWAXVIIEBN-UHFFFAOYSA-N Trifluoroethanol Chemical compound OCC(F)(F)F RHQDFWAXVIIEBN-UHFFFAOYSA-N 0.000 description 1
AUNAPVYQLLNFOI-UHFFFAOYSA-L [Pb++].[Pb++].[Pb++].[O-]S([O-])(=O)=O.[O-][Cr]([O-])(=O)=O.[O-][Mo]([O-])(=O)=O Chemical compound [Pb++].[Pb++].[Pb++].[O-]S([O-])(=O)=O.[O-][Cr]([O-])(=O)=O.[O-][Mo]([O-])(=O)=O AUNAPVYQLLNFOI-UHFFFAOYSA-L 0.000 description 1
238000005299 abrasion Methods 0.000 description 1
239000002253 acid Substances 0.000 description 1
239000000654 additive Substances 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
SOIFLUNRINLCBN-UHFFFAOYSA-N ammonium thiocyanate Chemical compound [NH4+].[S-]C#N SOIFLUNRINLCBN-UHFFFAOYSA-N 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
125000001769 aryl amino group Chemical group 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
239000000987 azo dye Substances 0.000 description 1
IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
238000009835 boiling Methods 0.000 description 1
FRLJSGOEGLARCA-UHFFFAOYSA-N cadmium sulfide Chemical class [S-2].[Cd+2] FRLJSGOEGLARCA-UHFFFAOYSA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
150000001868 cobalt Chemical class 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
238000010276 construction Methods 0.000 description 1
239000013078 crystal Substances 0.000 description 1
PGWFQHBXMJMAPN-UHFFFAOYSA-N ctk4b5078 Chemical class [Cd].OS(=O)(=O)[Se]S(O)(=O)=O PGWFQHBXMJMAPN-UHFFFAOYSA-N 0.000 description 1
PZABAVQEAVQKCD-UHFFFAOYSA-N cyano thiocyanate;potassium Chemical class [K].N#CSC#N PZABAVQEAVQKCD-UHFFFAOYSA-N 0.000 description 1
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
RAABOESOVLLHRU-UHFFFAOYSA-N diazene Chemical compound N=N RAABOESOVLLHRU-UHFFFAOYSA-N 0.000 description 1
229910000071 diazene Inorganic materials 0.000 description 1
239000000986 disperse dye Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
239000000945 filler Substances 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
125000002349 hydroxyamino group Chemical group [H]ON([H])[*] 0.000 description 1
150000002484 inorganic compounds Chemical class 0.000 description 1
229910010272 inorganic material Inorganic materials 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
235000013980 iron oxide Nutrition 0.000 description 1
VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
150000002739 metals Chemical class 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
125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
238000002156 mixing Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
238000012986 modification Methods 0.000 description 1
239000012860 organic pigment Substances 0.000 description 1
230000003372 organotropic effect Effects 0.000 description 1
DGBWPZSGHAXYGK-UHFFFAOYSA-N perinone Chemical compound C12=NC3=CC=CC=C3N2C(=O)C2=CC=C3C4=C2C1=CC=C4C(=O)N1C2=CC=CC=C2N=C13 DGBWPZSGHAXYGK-UHFFFAOYSA-N 0.000 description 1
230000000737 periodic effect Effects 0.000 description 1
FVDOBFPYBSDRKH-UHFFFAOYSA-N perylene-3,4,9,10-tetracarboxylic acid Chemical compound C=12C3=CC=C(C(O)=O)C2=C(C(O)=O)C=CC=1C1=CC=C(C(O)=O)C2=C1C3=CC=C2C(=O)O FVDOBFPYBSDRKH-UHFFFAOYSA-N 0.000 description 1
WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 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
235000021395 porridge Nutrition 0.000 description 1
230000001376 precipitating effect Effects 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Substances CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 1
239000004071 soot Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
230000002110 toxicologic effect Effects 0.000 description 1
231100000027 toxicology Toxicity 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/20—Compounding polymers with additives, e.g. colouring
- C08J3/22—Compounding polymers with additives, e.g. colouring using masterbatch techniques
- C08J3/226—Compounding polymers with additives, e.g. colouring using masterbatch techniques using a polymer as a carrier
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/20—Compounding polymers with additives, e.g. colouring
- C08J3/205—Compounding polymers with additives, e.g. colouring in the presence of a continuous liquid phase
- C08J3/21—Compounding polymers with additives, e.g. colouring in the presence of a continuous liquid phase the polymer being premixed with a liquid phase
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2377/00—Characterised by the use of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Derivatives of such polymers
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2477/00—Characterised by the use of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Derivatives of such polymers

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Compositions Of Macromolecular Compounds (AREA)
Processes Of Treating Macromolecular Substances (AREA)

DD24632382A 1981-12-23 1982-12-21 Verfahren zur herstellung von pigment- bzw. farbstoffpraeparaten DD207382A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH825281		1981-12-23

Publications (1)

Publication Number	Publication Date
DD207382A5 true DD207382A5 (de)	1984-02-29

Family

ID=4337498

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD24632382A DD207382A5 (de)	1981-12-23	1982-12-21	Verfahren zur herstellung von pigment- bzw. farbstoffpraeparaten

Country Status (4)

Country	Link
EP (1)	EP0083907A1 (cs)
JP (1)	JPS58117256A (cs)
CS (1)	CS235034B2 (cs)
DD (1)	DD207382A5 (cs)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2732257B2 (ja) *	1988-07-27	1998-03-25	鐘紡株式会社	優れた耐光堅牢性を有するポリアミド染色物及びその製造方法
DE10321788A1 (de)	2003-05-14	2004-12-09	Basf Ag	Polyamide

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CH368897A (de) *	1958-05-14	1963-04-30	Ciba Geigy	Verfahren zur Herstellung von farbstoffreichen Präparaten

1982
- 1982-12-17 EP EP82810550A patent/EP0083907A1/de not_active Withdrawn
- 1982-12-21 DD DD24632382A patent/DD207382A5/de unknown
- 1982-12-21 CS CS947282A patent/CS235034B2/cs unknown
- 1982-12-23 JP JP23508382A patent/JPS58117256A/ja active Pending

Also Published As

Publication number	Publication date
JPS58117256A (ja)	1983-07-12
CS235034B2 (en)	1985-04-16
EP0083907A1 (de)	1983-07-20

Publication	Publication Date	Title
EP0650939B1 (de)	1996-12-04	Verfahren zur Einfärbung von Baustoffen
DE3301357C1 (de)	1984-08-16	Markierungsmittel,Verfahren zu ihrer Herstellung und ihre Verwendung zur Markierung von feindispersen Systemen
EP1570006A1 (de)	2005-09-07	Feste pigmentzubereitungen, enthaltend pigmentderivate und oberflächenaktive additive
DE4336612C2 (de)	1995-09-07	Mehrstufiges Verfahren zur Herstellung von anorganischen Pigmentgranulaten und deren Verwendung zur Färbung von Kunststoffen und zur Herstellung von Pulverlacken
DE2933873A1 (de)	1980-03-13	Verfahren zur herstellung einer harzigen pigmentzubereitung
DE1266443B (de)	1968-04-18	Verfahren zur Herstellung von festen Pigmentpraeparaten fuer die Spinnfaerbung von Polyamiden
EP0008373A1 (de)	1980-03-05	Verfahren zur Herstellung einer Pigmentzubereitung, die erhaltene Pigmentzubereitung und damit in der Masse gefärbte lineare Polyester
DE60202244T2 (de)	2005-06-02	Leicht verteilbare Pigmentzusammensetzungen
DE2546936B2 (de)	1978-11-02	Präparate zum Färben thermoplastischer Polymerer in der Schmelze
DE2611756C2 (de)	1986-01-02	Granulate und Tabletten zur Modifizierung von in geschmolzenem Zustand formbaren Polykondensaten, deren Herstellungsverfahren und Verwendung
EP0229382B1 (de)	1992-06-10	Verfahren zur Herstellung stabilisierter Polyamide
DE2830159A1 (de)	1979-01-25	Verfahren zur herstellung von in waessrigen und/oder organischen medien leicht dispergierbaren, konzentrierten praeparaten in form von rieselfaehigen, staubarmen pulvern oder granulaten ausgehend von in wasser schwerloeslichen bis unloeslichen wirksubstanzen
EP0014503B1 (de)	1982-07-28	Verfahren zur Herstellung von in wässrigen Medien dispergierbaren, hochkonzentrierten, feindispersen, dispergiermittelarmen oder dispergiermittelfreien Präparaten von in Wasser schwer löslichen bis unlöslichen Wirksubstanzen in fester Form
JP2803731B2 (ja)	1998-09-24	粗製銅フタロシアニンをピグメント形態に転化する方法
DD207382A5 (de)	1984-02-29	Verfahren zur herstellung von pigment- bzw. farbstoffpraeparaten
DE1811021A1 (de)	1969-08-07	Pigmentpraeparate
DE1769488A1 (de)	1972-03-16	Pigmentzubereitungen
DE69106932T2 (de)	1995-06-08	Ein Verfahren zur Herstellung von Pigmenten.
DE1669612C3 (de)	1973-09-20	Leicht farbbare Polyolefinmassen
DE2027537C3 (de)	1980-07-10	Feste Farbstoffpräparate und deren Verwendung
DE1256886B (de)	1967-12-21	Polyamidpigmentmasse
DE3027577A1 (de)	1982-02-25	Pigmentpraeparationen, verfahren zu ihrer herstellung sowie ihre verwendung
DE2556421A1 (de)	1976-06-24	Verfahren zum faerben oder aufhellen linearer polyester in der masse
DE2504787C2 (de)	1983-06-23	Chromkomplexfarbstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung
DE1494737C (de)	1971-07-22	Verwendung von Phthalocyaninblau-Pigmenten der alpha-Modifikation zum Farben von Faden und Fasern aus synthetischen Polymeren