Process for the preparation of Quinacridone pigments

Claim 2

A process for the preparation of a pigment, mixed-crystal pigment or pigment preparation based on linear, unsubstituted quinacridones of β-phase or γ-phase, or substituted, linear quinacridones, which comprises: initially wet-milling a coarsely crystalline crude pigment in a liquid aqueous, aqueous-organic or organic medium in a stirred ball mill which is operated at a power density of more than 2.5 kW per liter of milling space and a peripheral stirrer speed of more than 12 m/s under the action of grinding media having a diameter of less than or equal to 0.9 mm, until fine division is reached, and then isolating the resulting pigment.

Claim 3

The process as claimed in claim 1, wherein grinding media having a diameter of from 0.2 to 0.9 mm are employed.

Claim 4

The process as claimed in claim 1, wherein grinding media having a diameter of from 0.3 to 0.5 mm are employed.

Claim 5

The process as claimed in claim 1, wherein the pigment concentration in the millbase is less than or equal to 40% by weight.

Claim 6

The process as claimed in claim 1, wherein the pigment concentration in the millbase is from 10 to 35% by weight.

Claim 7

The process as claimed in claim 1, wherein the pigment concentration in the millbase is from 10 to 20% by weight.

Claim 8

The process as claimed in claim 1, wherein the milling liquid is water, a C 1 -C 8 -alkanol, toluene, xylene, a C 1 -C 5 -dialkyl ketone, an aliphatic carboxamide or a mixture of the liquids mentioned.

Claim 9

The process as claimed in claim 1, wherein a crude, coarsely crystalline quinacridone pigment is employed which is substituted by halogen, alkyl, carboxamide, alkoxy groups or by a combination of said groups.

Claim 10

The process as claimed in claim 1, wherein unsubstituted quinacridone, 2,9-dimethyl-, 2,9-dichloro-, 3,10-dichloro-4,11-dichloro-or 4,11-dimethylquinacridone is employed.

Claim 11

The process as claimed in claim 1, wherein a crude, coarsely crystalline quinacridone mixed-crystal pigment is employed.

Claim 12

The process as claimed in claim 1, wherein the wet milling is carried out at a pH in the alkaline range.

Claim 13

The process as claimed in claim 1, wherein the solvent treatment is carried out with C 1 -C 8 -alkanols in aqueous medium.

Claim 14

The process as claimed in claim 1, wherein after wet-milling, the resulting pigment is subjected to a solvent treatment which is carried out with isobutanol in aqueous medium.

Claim 15

The process as claimed in claim 1, which comprises adding, at any desired point in time during the course of the process, one or more pigment dispersing agents of the formula (I) P--X.sub.m (I) in which m is a number from 1 to 4, P is the m-valent radical of linear, unsubstituted quinacridone or of linear 2,9-dimethylquinacridone, where X is a group of the formula (II) --COOM (II) or a group of the formula (III) --SO.sub.3 M (III) in which M is a hydrogen atom or one equivalent of an alkali metal ion, alkaline earth metal ion or ammonium ion, or X is a group of the formula (IV) ##STR9## or a group of the formula (V) ##STR10## in which R 1 and R 2 independently of one another are each a hydrogen atom, a C 1 -C 20 -alkyl, C 2 -C 20 -alkenyl or C 5 -C 7 -cycloalkyl group, or in which R 1 and R 2 together with the adjacent nitrogen atom form an aliphatic or aromatic five- or six-membered heterocyclic system including in each case from 1 to 3 ring members which are identical or different hetero atoms selected from the group consisting of nitrogen, oxygen and sulfur, R 3 is a hydrogen atom or a C 1 -C 4 -alkyl group, n is a number from 1 to 6 and o is the number 0 or 1, or X is the aminomethylene group of the formula (VI) ##STR11## or X is a group of the formula (VII) ##STR12## in which A is a five- or six-membered aromatic heterocycle which is optionally condensed and which comprises from 1 to 3 identical or different heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, and the heterocycle is attached to the methylene group via a carbon atom; R 6 and R 4 are a hydrogen atom, a C 1 -C 4 -alkyl, C 2 -C 4 -alkenyl or aryl group, or where R 6 and R 4 together form an aliphatic or aromatic ring, R 5 is a hydrogen atom or a C 1 -C 4 -alkyl, C 1 -C 3 -hydroxyalkyl or C 2 -C 4 -alkenyl group or X is a group of the formula (VIII) ##STR13## in which p is a number from 3 to 6, or X is the phthalimidomethylene group (IX) ##STR14## in which R 10 , R 8 and R 9 are a hydrogen fluorine chlorine or bromine atom and R 7 is a hydrogen, fluorine, chlorine or bromine atom or a nitro, C 1 -C 5 -alkyl, C 1 -C 6 -alkoxy or benzoylamino group, or X is the o-sulfobenzimidomethylene group (X) ##STR15## in which R 11 and R 12 independently of one another are a hydrogen, chlorine or bromine atom or a C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy or nitro group, or X is a group of the formula (XI) ##STR16## in which B is a carbonyl or sulfonyl group and q is the number 1 or 2, or pigment dispersing agents which comprise in one molecule various of the abovementioned substituents (II) to (XI).

Claim 16

The process as claimed in claim 14 wherein R 1 and R 2 together with the adjacent nitrogen atom form a piperidinyl, morpholinyl or pyrrolidinyl ring.

Claim 17

The process as claimed in claim 14, wherein in formula (VII) A is a radical of a heterocycle selected from the group consisting of imidazol, pyrrole, thiophene and furan.

Claim 18

The process as claimed in claim 14, wherein in formula (VII) R 6 and R 4 together with A form a benzimidazolyl, thionaphthenyl or indolyl ring.

Claim 19

The process as claimed in claim 14, wherein between 0.1 and 25% by weight, of the pigment dispersing agent of the formula (I) is employed, based on the crude pigment employed.

Claim 20

The process as claimed in claim 14, wherein from 3 to 12% by weight, of the pigment dispersing agent of the formula (I) is employed, based on the crude pigment employed.

Claim 21

A method of pigmenting lacquers, printing inks and plastics comprising the step of incorporating a pigment, mixed-crystal pigment or pigment preparation prepared as claimed in claim 1 into the lacquers, printing inks and plastics to be pigmented.

Claim 22

The process as claimed in claim 1, wherein after wet-milling a solvent treatment at a temperature of from 50° to 200° C. is performed.

Claim 23

A process for the preparation of a pigment, mixed-crystal pigment or pigment preparation based on linear, unsubstituted quinacridones of β-phase or γ-phase, or substituted, linear quinacridones, which comprises: initially wet-milling a coarsely crystalline crude pigment in a liquid aqueous or aqueous-organic medium in a stirred ball mill which is operated at a power density of more than 2.5 kW per liter of milling space and a peripheral stirrer speed of more than 12 m/s under the action of grinding media having a diameter of less than or equal to 0.9 mm, until fine division is reached, and then isolating the resulting pigment.

Claim 24

A process for the preparation of a pigment, mixed-crystal pigment or pigment preparation based on linear, unsubstituted quinacridones of β-phase or γ-phase, or substituted, linear quinacridones, which comprises: initially wet-milling a coarsely crystalline crude pigment in a liquid aqueous or aqueous-organic medium in a stirred ball mill which is operated at a power density of more than 2.5 kW per liter of milling space and a peripheral stirrer speed of more than 12 m/s under the action of grinding media having a diameter of less than or equal to 0.9 mm, until fine division is reached, and then isolating the resulting pigment.

Claim 25

The process as claimed in claim 1, wherein after the pigment undergoes wet-milling it is mixed with solvent and is heated at from 50° to 150° C. for from 1 to 6 hours.

Claim 26

The process as claimed in claim 1 wherein the pigment is based on linear, unsubstituted quinacridones of β-phase or γ-phase and the pigment prepared is substantially of the same phase as the initial coarsely crystalline crude pigment.