Processes for the preparation of titanium-phthalocyanine Type X

Claim 2

A process for the preparation of Type X titanyl phthalocyanine consisting of reacting titanium tetraalkoxide and diiminoisoindolene in the presence of a halonaphthalene solvent; dissolving the resulting Type I titanyl phthalocyanine in a trihaloacetic acid and an alkylene halide wherein alkylene contains from between 1 to about 6 carbon atoms; adding the resulting mixture slowly to a cold aqueous aliphatic alkane alcohol solution wherein alkane contains from 1 to about 12 carbon atoms; and thereafter isolating the resulting Type X titanyl phthalocyanine with an average volume particle size diameter of from about 0.05 to about 0.1 micron.

Claim 3

A process in accordance with claim 1 wherein the resulting mixture is slowly added to the aqueous alcohol solution over a period of time of from about 10 minutes to about 30 minutes.

Claim 4

A process in accordance with claim 1 wherein the resulting mixture is slowly added to the aqueous alcohol solution over a period of time of from about 20 minutes.

Claim 5

A process in accordance with claim 1 wherein said cold aqueous alcohol solution is comprised of an aliphatic alcohol and water.

Claim 6

A process in accordance with claim 1 wherein the alcohol is methanol.

Claim 7

A process in accordance with claim 1 wherein said cold aqueous alcohol solution is maintained at a temperature of from about zero to about a -10° C.

Claim 8

A process in accordance with claim 1 wherein there are selected titanium tetrabutoxide, 1,3-diiminoisoindolene, chloronaphthalene, methylene chloride, and trichloroacetic acid.

Claim 9

A process in accordance with claim 3 wherein the chloronaphthalene is 1-chloronaphthalene.

Claim 10

A process in accordance with claim 1 wherein the mixture resulting after the addition to said aqueous alcohol solution is maintained at a temperature of less than about 0° C.

Claim 11

A process in accordance with claim 1 wherein the resulting mixture is added dropwise to said cold aqueous alcohol solution.

Claim 12

A process in accordance with claim 10 wherein said aqueous alcohol solution is comprised of an aliphatic alcohol and water.

Claim 13

A process for the preparation of Type X titanyl phthalocyanine consisting of reacting titanium tetrabutoxide and diiminoisoindolene in the presence of a chloronaphthalene solvent; dissolving the resulting Type I titanyl phthalocyanine in a trihaloacetic acid and an alkylene halide wherein alkylene contains from between 1 to about 6 carbon atoms; adding the resulting mixture slowly to a cold aqueous aliphatic alkane alcohol solution wherein alkane contains from 1 to about 12 carbon atoms; maintaining the resulting mixture at a temperature of from about -10° to about 0° C.; and thereafter isolating the resulting Type X titanyl phthalocyanine with an average volume particle size diameter of from about 0.05 to about 0.1 micron.

Claim 14

A process for the preparation of Type X titanyl phthalocyanine consisting of reacting titanium tetrabutoxide and diiminoisoindolene in the presence of a chloronaphthalene solvent; dissolving the resulting Type I titanyl phthalocyanine in a trihaloacetic acid and an alkylene halide wherein alkylene contains from between 1 to about 6 carbon atoms; adding the resulting mixture slowly to a cold aqueous aliphatic alkane alcohol solution wherein alkane contains from 1 to about 12 carbon atoms; maintaining the resulting mixture at a temperature of from about -10° to about 0° C.; and thereafter isolating the resulting Type X titanyl phthalocyanine with an average volume particle size diameter of from about 0.05 to about 0.1 micron.

Claim 15

A process in accordance with claim 12 wherein the aqueous alcohol solution is comprised of water and methanol.

Claim 16

A process in accordance with claim 12 wherein the aqueous alcohol solution is comprised of water and methanol in a ratio of about 1:1.

Claim 17

A process in accordance with claim 12 wherein tetrabutoxide, 1-chloronaphthalene, 1,3-diiminoisoindolene, methylene chloride, and trichloroacetic acid are selected.

Claim 18

A process in accordance with claim 12 wherein the resulting mixture is added to said cold aqueous alcohol solution over a period of time of from about 10 to about 30 minutes.

Claim 19

A process for the preparation of Type IV titanyl phthalocyanine with an average particle size diameter of from about 0.05 to about 0.1 micron which comprises the treatment of the titanyl phthalocyanine Type X of claim 1 with a halobenzene.

Claim 20

A process in accordance with claim 17 wherein the halobenzene is chlorobenzene.

Claim 21

A process in accordance with claim 17 wherein the treatment comprises the addition of the Type X to the halobenzene.

Claim 22

A process in accordance with claim 17 wherein subsequent to said treatment there is isolated by filtration titanyl phthalocyanine Type IV.

Claim 23

A process in accordance with claim 1 wherein the Type I phthalocyanine is subjected to washing with dimethylformamide.

Claim 24

A process in accordance with claim 1 wherein the addition of the titanium tetraalkoxide is accomplished subsequent to dissolving the diiminoisoindolene in an organic solvent.

Claim 25

A process in accordance with claim 7 wherein the diiminoisoindolene is added in an amount of from about 1 part to about 10 parts for each part of titanium tetrabutoxide that is selected on a molar basis.

Claim 26

A process for the preparation of titanyl phthalocyanine consisting of adding titanium tetrabutoxide to 1,3-diiminoisoindolene in a 1-chloronaphthalene solvent; heating said mixture to reflux temperature of from about 130° to about 180° C.; removing any volatile byproducts by distillation thereby increasing the reflux temperature from about 180° to about 200° C.; maintaining the reaction mixture at said temperature for a time period of from about 0.5 to about 8 hours; followed by cooling the reaction mixture to a temperature of from about 130° to about 180° C. by removal of the heat source; and filtering said hot mixture to separate the solid titanyl phthalocyanine Type I product; dissolving the resulting Type I titanyl phthalocyanine in a trihaloacetic acid and an alkylene halide wherein alkylene contains from 1 to about 6 carbon atoms, adding the resulting mixture slowly to a cold aqueous aliphatic alkane alcohol solution, wherein alkane contains 1 to about 12 carbon atoms, and thereafter isolating the resulting Type X titanyl phthalocyanine with a average volume particle size diameter of from about 0.05 to about 0.1 micron.

Claim 27

A process for the preparation of titanyl phthalocyanine consisting of adding titanium tetrabutoxide to 1,3-diiminoisoindolene in a 1-chloronaphthalene solvent; heating said mixture to reflux temperature of from about 130° to about 180° C.; removing any volatile byproducts by distillation thereby increasing the reflux temperature from about 180° to about 200° C.; maintaining the reaction mixture at said temperature for a time period of from about 0.5 to about 8 hours; followed by cooling the reaction mixture to a temperature of from about 130° to about 180° C. by removal of the heat source; and filtering said hot mixture to separate the solid titanyl phthalocyanine Type I product; dissolving the resulting Type I titanyl phthalocyanine in a trihaloacetic acid and an alkylene halide wherein alkylene contains from 1 to about 6 carbon atoms, adding the resulting mixture slowly to a cold aqueous aliphatic alkane alcohol solution, wherein alkane contains 1 to about 12 carbon atoms, and thereafter isolating the resulting Type X titanyl phthalocyanine with a average volume particle size diameter of from about 0.05 to about 0.1 micron.

Claim 28

A process in accordance with claim 24 wherein isolation of the product is accomplished by filtration with a porcelain funnel fitted with a glass fiber filter.