Charge transport layer containing different aromatic diamine active charge transport compounds

Claim 2

An electrophotographic imaging member comprising a charge generating layer and a charge transport layer, said charge transport layer comprising a film forming binder, a first aromatic diamine represented by the general formula: ##STR10## wherein X is selected from the group consisting of an alkyl group containing from 1 to 4 carbon atoms and chlorine and a second aromatic diamine represented by the general formula: ##STR11## wherein R 1 represents an alkyl group or an alkoxy group, R 2 represents a hydrogen atom, an alkyl group an alkoxy group, a halogen atom, an alkoxycarbonyl group or a substituted amino group and R 3 represents an alkyl group an alkoxy group, a halogen atom, an alkoxycarbonyl group or a substituted amino group.

Claim 3

An electrophotographic imaging member according to claim 1 wherein said charge transport layer comprises N,N'-diphenyl-N,N'-bis-(alkylphenyl)-[1,1'-biphenyl[-4,4'diamine as said first diamine and a para substituted N,N,N',N'-tetraaryl-bitolyldiamine as said second diamine.

Claim 4

An electrophotographic imaging member according to claim 2 wherein said charge transport layer comprises between about 20 percent and about 80 percent by weight N,N'-diphenyl-N,N'-bis-(alkylphenyl)-[1,1'-biphenyl]-4,4'diamine and about 80 percent and about 20 percent by weight para substituted N,N,N',N'-tetraaryl-bitolydiamine based on the total weight of the aromatic diamines.

Claim 5

An electrophotographic imaging member according to claim 1 wherein said charge transport layer comprises between about 20 percent and about 80 percent by weight of said first aromatic diamine and about 80 percent and about 20 percent by weight of said second aromatic diamine based on the total weight of the aromatic diamines.

Claim 6

An electrophotographic imaging member according to claim 1 wherein said film forming binder is a polycarbonate resin.

Claim 7

An electrophotographic imaging member according to claim 1 wherein said charge transport layer comprises N,N'-diphenyl-N,N'-bis(3-methylphenyl)-(1,1'-biphenyl)-4,4'-diamine as said first diamine and N,N'-bis(4-methylphenyl)-N,N'-bis(4-ethylphenyl)-[3,3'-dimethyl-1,1'-biphenyl]-4,4'-diamine as said second diamine.

Claim 8

An electrophotographic imaging member according to claim 1 wherein said charge transport layer comprises N,N'-diphenyl-N,N'-bis(3-methylphenyl)-(1,1'-biphenyl)-4,4'-diamine as said first diamine and N,N,N',N'-Tetra-(4-methylphenyl)-[3,3'-dimethyl-1,1'-biphenyl]-4,4'-diamine as said second diamine.

Claim 9

An electrophotographic imaging process comprising providing an electrophotographic imaging member comprising a charge generating layer and a charge transport layer, said charge transport layer comprising a film forming binder, a first aromatic diamine represented by the general formula: ##STR12## wherein X is selected from the group consisting of an alkyl group containing from 1 to 4 carbon atoms and chlorine and a second aromatic diamine represented by the general formula: ##STR13## wherein R 1 represents an alkyl group or an alkoxy group, R 2 represents a hydrogen atom, an alkyl group, an alkoxy group, a halogen atom, an alkoxycarbonyl group or a substituted amino group and R 3 represents an alkyl group, an alkoxy group, a halogen atom, an alkoxycarbonyl group or a substituted amino group, depositing a uniform electrostatic charge on said imaging member with a corona charging device, exposing said imaging member to activating radiation in image configuration to form an electrostatic latent image on said imaging member, developing said electrostatic latent image with electrostatically attractable marking particles to form a toner image, transfering said toner image to a receiving member and repeating said depositing, exposing, developing and transfering steps for at least one hour until said corona charging device begins to emit oxides of nitrogen, temporarily stopping said depositing, exposing, developing and transfering steps for at least 10 minutes, and resuming said depositing, exposing, developing and transfering steps.

Claim 10

An electrophotographic imaging process comprising providing an electrophotographic imaging member comprising a charge generating layer and a charge transport layer, said charge transport layer comprising a film forming binder, a first aromatic diamine represented by the general formula: ##STR12## wherein X is selected from the group consisting of an alkyl group containing from 1 to 4 carbon atoms and chlorine and a second aromatic diamine represented by the general formula: ##STR13## wherein R 1 represents an alkyl group or an alkoxy group, R 2 represents a hydrogen atom, an alkyl group, an alkoxy group, a halogen atom, an alkoxycarbonyl group or a substituted amino group and R 3 represents an alkyl group, an alkoxy group, a halogen atom, an alkoxycarbonyl group or a substituted amino group, depositing a uniform electrostatic charge on said imaging member with a corona charging device, exposing said imaging member to activating radiation in image configuration to form an electrostatic latent image on said imaging member, developing said electrostatic latent image with electrostatically attractable marking particles to form a toner image, transfering said toner image to a receiving member and repeating said depositing, exposing, developing and transfering steps for at least one hour until said corona charging device begins to emit oxides of nitrogen, temporarily stopping said depositing, exposing, developing and transfering steps for at least 10 minutes, and resuming said depositing, exposing, developing and transfering steps.

Claim 11

An electrophotographic imaging process according to claim 8 wherein said charge transport layer comprises N,N'-diphenyl-N,N'-bis-(alkylphenyl)-[1,1'-biphenyl]-4,4'-diamine as said first diamine and a para substituted N,N,N',N'-tetraaryl-bitolyldiamine as said second diamine.

Claim 12

An electrophotographic imaging process according to claim 9 wherein said charge transport layer comprises between about 20 percent and about 80 percent by weight N,N'-diphenyl-N,N'-bis-(alkylphenyl)-[1,1'-biphenyl]-4,4'diamine and about 80 percent and about 20 percent by weight para substituted N,N,N',N'-tetraaryl-bitolyldiamine based on the total weight of the aromatic diamines.

Claim 13

An electrophotographic imaging process according to claim 8 wherein said charge transport layer comprises betwen about 20 percent and about 80 percent by weight of said first aromatic diamine and about 80 percent and about 20 percent by weight of said second aromatic diamine based on the total weight of the aromatic diamines.

Claim 14

An electrophotographic imaging process according to claim 8 wherein said film forming binder is a polycarbonate resin.

Claim 15

An electrophotographic imaging process according to claim 8 wherein said charge transport layer comprises N,N'-diphenyl-N,N'-bis(3-methylphenyl)-(1,1'-biphenyl)-4,4'-diamine as said first diamine and N,N'-bis(4-methylphenyl)-N,N'-bis(4-ethylphenyl)-[3,3'-dimethyl-1,1'-biphenyl]-4,4'-diamine as said second diamine.

Claim 16

An electrophotographic imaging process according to claim 8 wherein said charge transport layer comprises N,N'-diphenyl-N,N'-bis(3-methylphenyl)-(1,1'-biphenyl)-4,4'-diamine as said first diamine and N,N,N',N'-Tetra-(4-methylphenyl)-[3,3'-dimethyl-1,1'-biphenyl]-4,4'-diamine as said second diamine.