Process for the preparation of internal latent image type silver halide photographic emulsions

Claim 2

A process for the preparation of an internal latent image type silver halide emulsion containing silver halide grains comprising a central core of silver halide doped with metal ions, chemically sensitized or a combination thereof and an outer shell of silver halide covering at least light-sensitive sites of the central core, which process is characterized in that the surface of the silver halide grain is subjected to chemical sensitization in the presence of a homopolymer or copolymer to improve said surface chemical sensitization, said homopolymer containing a repeating unit represented by general formula (I) and said copolymer selected from the group consisting of copolymers obtained by copolymerization of only monomer units of the formula (I) and copolymers obtained by the copolymerization of a monomer unit of the formula (I) copolymerized with an addition-polymerizable ethylenically unsaturated compound: ##STR23## wherein R 1 is a hydrogen atom or an alkyl group, and Q is any one of groups (1) to (4) set forth below: ##STR24## wherein q is an integer of from 2 to 4, ##STR25## wherein R 2 and R 3 are each a hydrogen atom or an alkyl group, ##STR26## wherein Z 1 is a group of atoms required to a lactam ring, an oxazolidone ring or a pyridone ring, and A is a bond, ##STR27## wherein B is ##STR28## wherein R 4 is a hydrogen atom or an alkyl group, and l is an integer of from 1 to 6, ##STR29## wherein A is the same as defined for the above formula (3), D is a bond, --O--, or ##STR30## wherein R 5 is a hydrogen atom, an alkyl group or ##STR31## wherein R 6 is an alkyl group, and m and n are each an integer of from 1 to 6 and m+n is from 4 to 7; and wherein said homopolymer is present in an amount of from 0.002 to 1 g per mol of silver or said copolymer is present in an amount providing 0.002 to 1 g of the repeating unit of the formula (I) per mol of silver.

Claim 3

The process as recited in claim 1, wherein R 1 is a hydrogen atom.

Claim 4

The process as recited in claim 2 wherein Q represents a group selected from the group consisting of the following (i)-(iii): ##STR32## wherein R 2 represents a methyl group or an ethyl group, and R 3 represents a hydrogen atom, a methyl group or an ethyl group ##STR33## wherein A represents a single bond or ##STR34## and Z 1 forms a 5-membered or 6-membered lactam ring or an oxazolidone ring.

Claim 5

The process as recited in claim 3, wherein Q represents ##STR35## a pyrrolidone group or an oxazolidone group.

Claim 6

The process as recited in claim 4, wherein Q represents a pyrrolidone group.

Claim 7

The process as recited in claim 1, wherein said chemical sensitization occurs in the presence of said homopolymer.

Claim 8

The process as recited in claim 1, wherein said chemical sensitization occurs in the presence of said copolymer.

Claim 9

The process recited in claim 1 wherein said homopolymer or copolymer has a molecular weight of about 2000 or more.

Claim 10

The process as recited in claim 1, wherein said homopolymer or copolymer is selected from a group consisting of poly-(N-vinylpyrrolidone), poly-(N-vinyloxazolidone), poly-(N-vinylsuccinimide), poly-(N-vinylglutarimide), poly(N-vinylpiperidone), poly-(N-vinyl-ε-caprolactam), poly(N-methyl-N-vinylacetamide), poly-(N-ethyl-N-vinylacetamide), poly-(N-vinylacetamide), vinyl alcohol-N-vinyl acetamide copolymer (molar ratio: 30:70), vinly alcohol-N-vinylpyrrolidone copolymer (molar ratio: 20:80), vinyl alcohol-N-vinylpyrrolidone copolymer (molar ratio: 30:70), N-vinylpyrrolidone-vinyl acetate copolymer (molar ratio: 70:30), N-vinylpyrrolidone-2-hydroxyethyl-acrylate copolymer (molar ratio: 70:30), N-vinylpyrrolidone-acrylic acid copolymer (molar ratio: 90:10), N-vinylpyrrolidone-N-vinyl-3,5-dimethyltriazole copolymer (molar ratio: 50:50), N-vinylpiperidone-2-methoxyethyl acrylate copolymer (molar ratio: 70:30), N-vinylpiperidone-methyl vinyl ether copolymer (molar ratio: 90:10), N-vinyloxazolidone-vinyl alcohol copolymer (molar ratio: 65:35), N-vinyloxazolidoneacrylic acid copolymer (molar ratio: 80:20), N-vinylpyrrolidone-N-vinylpiperidone-2-hydroxyethyl acrylate copolymer (molar ratio: 40:30:30), vinyl alcohol-vinyl acetate-N-vinyl-2-pyridone copolymer (molar ratio: 70:25:5), N-vinylpyrrolidone-2-hydroxyethyl acrylate-vinyl acetate copolymer (molar ratio: 70:20:10), N-vinylpyrrolidone vinyl-alcohol vinyl propionate sodium styrenesulfonate copolymer (molar ratio: 40:40:5:15), N-vinylpyrrolidoneacrylamide copolymer (molar ratio: 60:40), N-vinylpyrrolidone-2-acrylamide-2-methylpropane-sulfonic acid copolymer (molar ratio: 75:25), N-vinylpiperidone-acrylamide copolymer (molar ratio: 60:40), N-vinyloxazolidone-N-(2-hydroxyethyl)acrylamide copolymer (molar ratio: 70:30), N-vinylpyrrolidone-N-vinylmorpholine-acrylamide copolymer (molar ratio: 50:20:30), N-vinylsuccinimide-N-vinyl-ε-caprolactam-acrylamide copolymer (molar ratio: 40:20:40), N-vinyloxazolidone-acrylamide-acrylic acid copolymer (molar ratio: 60:20:20), N-vinylpyrrolidone-acrylamide-vinyl acetate-acrylic acid copolymer (molar ratio: 60:20:10:10), and N-vinylpyrrolidone-dimethylacrylamide copolymer (molar ratio: 70:30).

Claim 11

The process as recited in claim 1 wherein the amount of homopolymer or copolymer added is from 0.002 to 0.5 g calculated as the amount of the repeating unit of the general formula (I) in the homopolymer or copolymer per mol of silver.

Claim 12

The process as recited in claim 10 wherein the amount of homopolymer or copolymer added is from 0.002 to 0.2 g calculated as the amount of the repeating unit of the general formula (I) in the homopolymer or copolymer per mol of silver.