Phthalocyanine treatment process

Claim 2

A process for preparing vanadyl phthalocyanine for electrophotographic devices comprising a (a) crude vanadyl phthalocyanine pigment synthesis phase comprising reacting vanadium pentoxide and phthalonitrile to form vanadyl phthalocyanine pigment and other reaction products, separating crude vanadyl phthalocyanine pigment from said other reaction products, drying said crude vanadyl phthalocyanine pigment; (b) a dried, partially purified vanadyl phthalocyanine pigment preparation, permutoid swelling phase comprising mixing said crude vanadyl phthalocyanine pigment with between about 60 percent and about 80 percent by weight solution of H 2 SO 4 to form an H 2 SO 4 -vanadyl phthalocyanine pigment mixture, diluting with agitation said H 2 SO 4 -vanadyl phthalocyanine pigment mixture with deionized water while maintaining the dilution temperature between about -20° C. and about +5° C. to form a diluted mixture, separating the vanadyl phthalocyanine pigment by filtration, washing the isolated vanadyl phthalocyanine pigment particles, and drying said vanadyl phthalocyanine pigment to form said dried, partially purified vanadyl phthalocyanine pigment; and (c) a purified vanadyl phthalocyanine pigment preparation, acid pasting phase comprising dissolving said dried, partially purified vanadyl phthalocyanine pigment in at least 94 percent concentrated H 2 SO 4 to form a solution of vanadyl phthalocyanine in concentrated H 2 SO 4 , adding said solution of vanadyl phthalocyanine in concentrated H 2 SO 4 to water while maintaining said solution at a temperature of between about 0° C. and about 5° C. to precipitate said vanadyl phthalocyanine as vanadyl phthalocyanine pigment particles, separating the precipitated vanadyl phthalocyanine pigment particles from said H 2 SO 4 and water to isolate said vanadyl phthalocyanine pigment particles, washing said vanadyl phthalocyanine pigment particles with water free of any base, and drying said vanadyl phthalocyanine pigment particles to form said purified vanadyl phthalocyanine pigment.

Claim 3

A process for preparing vanadyl phthalocyanine for electrophotographic devices according to claim 1 including, in said permutoid swelling phase, diluting with deionized water said H 2 SO 4 -vanadyl phthalocyanine pigment mixture while maintaining the temperature of said H 2 SO 4 -vanadyl phthalocyanine pigment mixture between about -20° C. and about +5° C. with continuous cooling and agitation to form said partially purified vanadyl phthalocyanine pigment prior to any filtration and washing steps, separating said partially purified vanadyl phthalocyanine pigment from said other reaction products, and washing said pigment cake with solvents prior to drying said pigment cake of partially purified vanadyl phthalocyanine pigment.

Claim 4

A process for preparing vanadyl phthalocyanine for electrophotographic devices according to claim 2 including, in said permutoid swelling phase, diluting with said deionized water said H 2 SO 4 -vanadyl phthalocyanine pigment mixture to a dilution of between about 20 percent and about 50 percent by weight aqueous H 2 SO 4 while maintaining the dilution temperature between about -20° C. and about +5° C.

Claim 5

A process for preparing vanadyl phthalocyanine for electrophotograhic devices according to claim 3 including, in said permutoid swelling phase, diluting with said deionized water said H 2 SO 4 -vanadyl phthalocyanine pigment mixture to a dilution of between about 30 percent and about 45 percent by weight aqueous H 2 SO 4 while maintaining the dilution temperature between about -5° C. and about +4° C.

Claim 6

A process for preparing vanadyl phthalocyanine for electrophotographic devices according to claim 1 wherein the washing agent for said washing of said vanadyl phthalocyanine pigment particles during said acid pasting phase is deionized water.

Claim 7

A process for preparing vanadyl phthalocyanine for electrophotographic devices according to claim 2 including washing the vanadyl phthalocyanine pigment particles isolated during said acid pasting phase with deionized water free of ammonium hydroxide, and drying said pigment particles.

Claim 8

A process for preparing vanadyl phthalocyanine for electrophotographic devices according to claim 5 wherein, in said permutoid swelling phase, said mixing of said crude vanadyl phthalocyanine pigment with said H 2 SO 4 to form said H 2 SO 4 -vanadyl phthalocyanine pigment mixture is performed at a temperature between about 0° C. and about 25° C. and said diluting of said H 2 SO 4 -vanadyl phthalocyanine pigment mixture with said deionized water to form vanadyl phthalocyanine pigment is carried out while maintaining the dilution temperature between about -5° C. and about +4° C.

Claim 9

A process for preparing vanadyl phthalocyanine for electrophotographic devices according to claim 5 including, in said acid pasting phase, slurry washing said vanadyl phthalocyanine pigment particles separated from said H 2 SO 4 and water by filtration with cold deionized water at least once followed by washing said vanadyl phthalocyanine pigment particles with hot deionized water, prior to drying said pigment particles.

Claim 10

A process for preparing vanadyl phthalocyanine for electrophotographic devices according to claim 6 including, in said acid pasting phase, slurry washing said vanadyl phthalocyanine pigment particles separated from said H 2 SO 4 and water by filtration with cold deionized water and washing said vanadyl phthalocyanine pigment particles with hot deionized water.

Claim 11

A process for preparing vanadyl phthalocyanine for electrophotographic devices according to claim 6 wherein, in said permutoid swelling phase, said mixing of said crude vanadyl phthalocyanine pigment with said H 2 SO 4 to form said H 2 SO 4 -vanadyl phthalocyanine pigment mixture is performed at a temperature between about 0° C. and about 25° C. and said diluting of said H 2 SO 4 -vanadyl phthalocyanine pigment mixture with said deionized water to form vanadyl phthalocyanine pigment is carried out while maintaining the dilution temperature between about -5° C. and about +4° C.

Claim 12

A process for preparing vanadyl phthalocyanine for electrophotographic devices according to claim 1 including, in said acid pasting phase, adding said solution of vanadyl phthalocyanine in said concentrated H 2 SO 4 to deionized water in order to precipitate said vanadyl phthalocyanine as vanadyl phthalocyanine pigment particles while maintaining said solution at a temperature of between about 0° C. and about +5° C.

Claim 13

A process for preparing vanadyl phthalocyanine for electrophotographic devices comprising a (a) crude vanadyl phthalocyanine pigment synthesis phase comprising reacting vanadium pentoxide and phthalonitrile to form vanadyl phthalocyanine pigment and other reaction products, separating crude vanadyl phthalocyanine pigment from said other reaction products, drying said crude vanadyl phthalocyanine pigment; (b) a dried, partially purified vanadyl phthalocyanine pigment preparation, permutoid swelling phase comprising mixing said crude vanadyl phthalocyanine pigment with an about 60 percent to about 80 percent by weight solution of H 2 SO 4 at a temperature between about 0° C. and about 25° C. to form an H 2 SO 4 -vanadyl phthalocyanine pigment mixture, diluting with agitation said H 2 SO 4 -vanadyl phthalocyanine pigment mixture with deionized water to a dilution of between about 20 percent and about 50 percent by weight aqueous H 2 SO 4 while maintaining the dilution temperature between about -20° C. and about +5° C. to form form the vanadyl phthalocyanine pigment prior to any filtration and washing steps, separating the vanadyl phthalocyanine pigment by filtration, washing the isolated vanadyl phthalocyanine pigment particles, drying said vanadyl phthalocyanine particles to form said dried, partially purified vanadyl phthalocyanine pigment; and (c) a purified vanadyl phthalocyanine pigment preparation acid pasting phase comprising dissolving said dried, partially purified vanadyl phthalocyanine pigment in at least 94 percent by weight concentrated H 2 SO 4 to form a solution of vanadyl phthalocyanine in concentrated H 2 SO 4 , adding said solution of vanadyl phthalocyanine in concentrated H 2 SO 4 to deionized water while maintaining said solution at a temperature of between about 0° C. and about +5° C. to precipitate said vanadyl phthalocyanine as vanadyl phthalocyanine pigment particles, separating the precipitated vanadyl phthalocyanine pigment particles from said H 2 SO 4 and water to isolate said vanadyl phthalocyanine pigment particles, slurry washing said vanadyl phthalocyanine pigment particles with deionized water at about room temperature at least once, washing said vanadyl phthalocyanine pigment particles with deionized water free of any base at about room temperature, washing said vanadyl phthalocyanine pigment particles with water free of any base and at a temperature of between about 70° C. and about 85° C. until the wash effluent has a conductivity of less than about 10 micromhos, and drying said vanadyl phthalocyanine pigment particles to form said purified vanadyl phthalocyanine pigment.

Claim 14

A process for preparing vanadyl phthalocyanine for electrophotographic devices comprising a (a) crude vanadyl phthalocyanine pigment synthesis phase comprising reacting vanadium pentoxide and phthalonitrile to form vanadyl phthalocyanine pigment and other reaction products, separating crude vanadyl phthalocyanine pigment from said other reaction products, drying said crude vanadyl phthalocyanine pigment; (b) a dried, partially purified vanadyl phthalocyanine pigment preparation, permutoid swelling phase comprising mixing said crude vanadyl phthalocyanine pigment with an about 60 percent to about 80 percent by weight solution of H 2 SO 4 at a temperature between about 0° C. and about 25° C. to form an H 2 SO 4 -vanadyl phthalocyanine pigment mixture, diluting with agitation said H 2 SO 4 -vanadyl phthalocyanine pigment mixture with deionized water to a dilution of between about 20 percent and about 50 percent by weight aqueous H 2 SO 4 while maintaining the dilution temperature between about -20° C. and about +5° C. to form form the vanadyl phthalocyanine pigment prior to any filtration and washing steps, separating the vanadyl phthalocyanine pigment by filtration, washing the isolated vanadyl phthalocyanine pigment particles, drying said vanadyl phthalocyanine particles to form said dried, partially purified vanadyl phthalocyanine pigment; and (c) a purified vanadyl phthalocyanine pigment preparation acid pasting phase comprising dissolving said dried, partially purified vanadyl phthalocyanine pigment in at least 94 percent by weight concentrated H 2 SO 4 to form a solution of vanadyl phthalocyanine in concentrated H 2 SO 4 , adding said solution of vanadyl phthalocyanine in concentrated H 2 SO 4 to deionized water while maintaining said solution at a temperature of between about 0° C. and about +5° C. to precipitate said vanadyl phthalocyanine as vanadyl phthalocyanine pigment particles, separating the precipitated vanadyl phthalocyanine pigment particles from said H 2 SO 4 and water to isolate said vanadyl phthalocyanine pigment particles, slurry washing said vanadyl phthalocyanine pigment particles with deionized water at about room temperature at least once, washing said vanadyl phthalocyanine pigment particles with deionized water free of any base at about room temperature, washing said vanadyl phthalocyanine pigment particles with water free of any base and at a temperature of between about 70° C. and about 85° C. until the wash effluent has a conductivity of less than about 10 micromhos, and drying said vanadyl phthalocyanine pigment particles to form said purified vanadyl phthalocyanine pigment.