Process for the production of copper phthalocyanine pigment preparations of the α phase

Claim 2

A process for the preparation of a copper phthalocyanine pigment of the α phase or a pigment preparation based on a copper phthalocyanine pigment of the α phase, which comprises a) first wet milling a crude copper phthalocyanine pigment, which is predominantly present in the phase in an aqueous 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 speed of the stirrer of more than 12 m/s with exposure to a grinding medium having a diameter of less than 1 mm under phase-converting conditions, thus producing a prepigment composition, then b) subjecting the prepigment composition obtained by a) either b1) in the form of the mill base suspension thus obtained, or b2) after addition of an organic solvent to the mill base suspension obtained by a), or b3) in the case where the prepigment intermediate or the prepigment composition intermediate is isolated, after first taking it up in an inert organic solvent, to a finishing treatment at elevated temperature, and c) then isolating the resulting pigment or pigment preparation.

Claim 3

The process as claimed in claim 1, wherein there is added one or more times, before, during or after one or more of the individual steps a), b) and c), at least one pigment dispersing agent of the formula (I), P--X.sub.m (I) in which P is an m-valent radical based on the formula (II) ##STR10## in which m is from 1 to 6, Me is two hydrogen atoms or a divalent metal atom, and X is a group of the formula (IIIa) --COOM (IIIa) or a group of the formula (IIIb) --SO.sub.3 M (IIIb) in which M is a hydrogen atom or an equivalent of an alkali metal ion, alkaline earth metal ion or ammonium ion or in which X is a group of the formula (IIIc) ##STR11## or a group of the formula (IIId) ##STR12## in which R 1 and R 2 are identical or different and are a hydrogen atom, a C 1 -C 20 -alkyl, C 2 -C 20 -alkenyl group or a 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- to seven-membered heterocyclic system having in each case 1 to 3 identical or different heteroatoms belonging to the ring selected from the series consisting of nitrogen, oxygen and sulfur, R 3 is a hydrogen atom or a C 1 -C 4 -alkyl group, n is from 1 to 6, o is 0 or 1, and m is from 1 to 4, or in which x is an aminomethylene group of the formula (IIIe) ##STR13## in which R 1 and R 2 have the abovementioned meaning and m is from 1 to 6, or in which X is a group of the formula (IIIf) ##STR14## in which A is a five- or six-membered aromatic ring or a fused aromatic heterocycle containing 1 to 3 identical or different heteroatoms selected from the series consisting of nitrogen, oxygen and sulfur, and the heterocycle is bound to the methylene group via a carbon atom, R 30 and R 4 are a hydrogen atom, a C 1 -C 4 -alkyl, C 1 -C 4 -hydroxyalkyl or a C 2 -C 4 -alkenyl group or C 2 H 4 OH or an aryl group, aryl being phenyl which is unsubstituted or substituted by 1 to 4 radicals selected from the group consisting of C 1 -C 6 -alkyl, halogen, C 1 -C 6 -alkoxy, cyano, CONH 2 and COOR 12 , R 12 being hydrogen or C 1 -C 6 -alkyl, R 30 and R 4 together can also form an aliphatic or aromatic ring, R 5 is a hydrogen atom, a C 1 -C 4 -alkyl, a C 1 -C 3 -hydroxyalkyl or a C 2 -C 4 -alkenyl group and m is from 1 to 4, or in which X is a group of the formula (IIIg) ##STR15## p being from 3 to 6 and m being from 1 to 4, or in which X is a phthalimidomethylene group of the formula (IIIh) ##STR16## in which R 6 , R 8 and R 9 are identical or different and are a hydrogen, fluorine, chlorine or bromine atom, R 7 is hydrogen, fluorine, chlorine or bromine atom or a nitro, C 1 -C 6 -alkoxy or benzoylamino group, and m is from 1 to 4, or in which X is an o-sulfobenzimidomethylene group of the formula (IIIi) ##STR17## in which R 10 and R 11 are identical or different and are a hydrogen, chlorine or bromine atom or a C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy or a nitro group, and m is from 1 to 4, or in which X is a group of the formula (IIIk) ##STR18## in which B is a carbonyl or sulfonyl group, and R 1 , R 2 and R 3 have the abovementioned meaning, q is 1 or 2, and m is from 1 to 4, or there is added at least one pigment dispersing agent of the formula (I) containing variants of the abovementioned radical X in one molecule.

Claim 4

The process as claimed in claim 1, wherein there is added one or more times, before, during or after one or more of the individual steps a), b) and c), at least one pigment dispersing agent of the formula (I), P--X.sub.m (I) in which P is an m-valent radical based on the formula (II) ##STR19## in which m is from 1 to 6, Me is two hydrogen atoms or a copper, iron, zinc, nickel, cobalt or tin atom, and X is a group of the formula (IIIa) --COOM (IIIa) or a group of the formula (IIIb) --SO.sub.3 M (IIIb) in which M is a hydrogen atom or an equivalent of an alkali metal ion, alkaline earth metal ion or ammonium ion or in which X is a group of the formula (IIIc) ##STR20## or a group of the formula (IIId) ##STR21## in which R 1 and R 2 are identical or different and are a hydrogen atom, a methyl or ethyl group or in which R 1 and R 2 together with the adjacent nitrogen atom from an imidazole, piperidine, piperazine, pyrrolidine, morpholine, imidazoline or hexamethylene ring, R 3 is a hydrogen atom or a methyl group n is 2 or 3, o is 1 and m is from 1 to 4, or in which X is an aminomethylene group of the formula (IIIe) ##STR22## in which R 1 and R 2 have the abovementioned meaning and m is from 1 to 6, or in which X is a group of the formula (IIIf) ##STR23## in which A is an imidazole, triazole or pyrazole ring and said heterocycle is bound to the methylene group via a carbon atom, R 30 and R 4 are a hydrogen atom, methyl, ethyl or C 2 H 4 OH or an aryl group, aryl being phenyl which is unsubstituted or substituted by 1 to 4 radicals selected from the group consisting of C 1 -C 6 -alkyl, F, Cl, Br, C 1 -C 6 -alkoxy, cyano, CONH 2 and COOR 12 , R 12 being hydrogen or C 1 -C 6 -alkyl, R 30 and R 4 together optionally form an aliphatic or a phenyl ring, R 5 is a hydrogen atom, a C 1 -C 4 -alkyl, a C 1 -C 3 -hydroxyalkyl or a C 2 -C 4 -alkenyl group and m is from 1 to 4, or in which X is a group of the formula (IIIg) ##STR24## p being from 3 to 5 and m being from 1 to 4, or in which X is a phthalimidomethylene group of the formula (IIIh) ##STR25## in which R 6 , R 7 , R 8 and R 9 are hydrogen atoms, and m is from 1 to 4, or in which X is an o-sulfobenzimidomethylene group of the formula (IIIi) ##STR26## in which R 10 and R 11 are a hydrogen atom and m is from 1 to 4, or in which X is a group of the formula (IIIk) ##STR27## in which B is a carbonyl group, and R 1 , R 2 and R 3 have the abovementioned meaning, q is 1 and m is from 1 to 4, or there is added at least one pigment dispersing agent of the formula (I) containing variants of the abovementioned radical X in one molecule.

Claim 5

The process as claimed in claim 2, wherein Me is a cooper atom.

Claim 6

The process as claimed in claim 1, wherein a grinding medium of diameter 0.2 to 1.0 mm is used.

Claim 7

The process as claimed in claim 1, wherein a grinding medium of diameter 0.3 to 0.5 mm is used.

Claim 8

The process as claimed in claim 1, wherein the ratio of milling space to surface area of the milling space in the stirred ball mill is less than 0.15:1 (dm 3 :dm 2 ).

Claim 9

The process as claimed in claim 1, wherein the pigment concentration in the mill base suspension is at most 40% by weight.

Claim 10

The process as claimed in claim 1, wherein the pigment concentration in the mill base suspension is 10 to 30% by weight.

Claim 11

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

Claim 12

The process as claimed in claim 1, wherein wet milling is carried out in a neutral or in an alkaline pH range.

Claim 13

The process as claimed in claim 1, wherein the finishing treatment is carried out in a mixture of water and an alkanol.

Claim 14

The process as claimed in claim 1, wherein the finishing treatment is carried out in a mixture of water and a butanol.

Claim 15

The process as claimed in claim 1, wherein highly crystalline copper phthalocyanine crude pigments of the β phase are used which optionally still contain small amounts of carboxyl or sulfonyl groups.

Claim 16

The process as claimed in claim 1, wherein at least one compound of the formula (I) in which X is a phthaloimidomethylene group of the formula (IIIh) ##STR28## R 6 , R 7 , R 8 , and R 9 being each a hydrogen atom and m being from 1 to 4, is used as the pigment dispersing agent.

Claim 17

The process as claimed in claim 1, wherein at least one compound of the formula (I) in which X is an o-sulfobenzimidomethylene group of the formula (IIIi) ##STR29## R 10 and R 11 being each a hydrogen atom and m being from 1 to 4, is used as the pigment dispersing agent.

Claim 18

The process as claimed in claim 1, wherein at least one compound of the formula (I) in which X is a group of the formula (IIIf) ##STR30## in which A is an imidazole, triazole or pyrazole radical and the heterocycle mentioned is bound to the methylene group via a carbon atom, R 30 and R 4 are a hydrogen atom, a methyl, ethyl or C 2 H 4 OH group or in which R 30 and R 4 together form a phenyl radical, R 5 is a hydrogen atom, a C 1 -C 4 -alkyl, C 1 -C 3 -hydroxyalkyl or a C 2 -C 4 -alkenyl group and m is from 1 to 4, is used as the pigment dispersing agent.

Claim 19

The process as claimed in claim 1, wherein a mixture of different pigment dispersing agents of the formula (I) is used.

Claim 20

The process as claimed in claim 1, wherein the pigment dispersing agents of the formula (I) are present in amounts of 0.1 to 25% by weight, relative to the copper phthalocyanine pigment used.

Claim 21

The process as claimed in claim 1, wherein the pigment dispersing agents of the formula (I) are present in amounts of 0.1 to 15% by weight, relative to the copper phthalocyanine pigment used.

Claim 22

The process as claimed in claim 1, wherein the pigment dispersing agents of the formula (I) are present in amounts of 3 to 10% by weight, relative to the copper phthalocyanine pigment used.

Claim 23

A pigment preparation obtained by the process as claimed in claim 1.

Claim 24

A method of pigmenting a varnish, a printing ink or a plastic, comprising the step of incorporating a pigment preparation as claimed in claim 1 into said varnish, printing ink or plastic.