AU596149B2 - Color-image forming process - Google Patents

Description

PCT

44f"*tAtl Ake-] tit: M E a (m'1 000 4 A(1)NQ#*WO 87/ 04809 G03C 7/30, 7/26 A I)u~# (43) SO-DR 5 1987-8JE13E (13.08.87) (21) LBW Wq#-5 PcT/JP87/00062 (22) L@f;,q.W W 1987-TIA29S (29, 01, 87) (32) -B 198VF1A30E3 (30. 01. 86) (33) 44 Jp (FUJI PHOTO FILM COMPANY LIMITED)CJP/JP) f250-01 1 OJIk Kariagawa, (JP) (7 2) 31 Al (TAKAHASHI, Osamu) CJP/JP) WWM (NARUSE, Hideaki)CJP/JP) AT (ARAKAWVA, Juri)CJP/JP) dWnoO~ (YAMAGUCHI, J I ra) (JP/JP) ~7X±V 74 WAW K a na ga wa, J P (74) ftI3jA A &SAKI, KIyo0t a k a e ti 1, (81) 192 oo B I T NL 1: S, Ali tliapm This document contains tile am endm1ts 1niade Lld(& SSection 49 and is recfo 2 4 SEP 1187 (54)TIle: COLOR Wr GE FORMING PROCESS (57) Abstract A color image-Cor-ning process which comprises processing an imagewise expaose i c'olor paper containing an anionic surfactant having a orne-substitu ted aliphatic group as a hydrophobic group and ao .SO 3 M or 'OSOIM group (wherein M represents hydrogen or cation) as a hydrophilic group with a substantially benzyl alcohol-free color developer, In the case of processing the above~described color paper containing the fluorine-substituted anlonic surraclant, color images with high coloraton density can be obtained in a short time even when the paper is processed with a ,olof developer which substantially does not. contain a development promoter causing environtnintal pollution.

I

(S7) Pc -S O3 3 Mtkd-O SO3M M/)m AT f-7, V7 FR 7 :jMR e 7 BB 11 Cl I 7B 71~J N.L t >X1 BE U OG 7:;)IilV 7 IT !ft 1) RO 1) 7.7 BJ It Z' JPE SD A BR /-JI vq01 P 0 SE A 7:C~ CF *77 U j A1 Q C KR ;KaL SN cc :0 LI 1 2 SU v L,:r-AA CII A LIC 7, -9 TO CM it LI I JE't J TG I- -C DE M 4 KC US us DK Zl- rMG 7 r J M FT '7 4'f AL o 1

SPECIFICATION

Il COLOR IMAGE-FORMING PROCESS ij [TECHNICAL FIELD] SThis invention relates to a color image-forming process using silver halide color light-sensitive materials and, particularly, to a color image-forming process with shortened processing time and using substantially no benzyl jalcohol.

[BACKGROUND ART] For forming color photographic images, yellow, magenta, and cyan 3-color photographic couplers are incorporated in light-sensitive layers and after light-exposure, the layers are processed by a color developer containing a color developing agent. In this course, colored dyes are formed by the coupling reaction of the oxidation product of an aromatic primary amine and the couplers and in this case, it is necessary to give high color density as possible in a limited development time.

High color density is usually achieved by using couplers having a high coupling speed as possible, a silver halide emulsion which is liable to be developed and gives a large amount of developed silver per unit coated amount thereof, or a color developer showing high developing speed.

-r 1 2 For hastening the development of silver halide emulsion, it is easily considered to increase the content of silver chloride in the silver halide but the increase of the content of silver chloride gives faults that the sensitivity is reduced and fog is liable to occur. Also, for increasing the developed silver amount, it may be considered to increase the content of silver chloride as described above or intensify a chemical sensitization but this case also has a fault that fog is liable to occur. It is also a means for hastening development to reduce the grain size of silver halide emulsion but this has a fatal fault that a sensitivity is reduced. A method of using a silver chloride emulsion is described, for example, in Unexamined Published Japanese Patent Application Nos. 95345/83, 232342/84, and 19140/85 but there is a problem that the control of gradation is difficult.

On the other hand, various counterplans have hitherto been made on color developer for hastening the development. Among them, various kinds of additives have been investigated for accelerating coloring by hastening the permeation of a color developing agent into color couplerdispersed oil drops, and, in particular, a method of hastening color development by adding benzyl alcohol to color developer has a large coloring accelerating effect and hence has now been widely used for processing color photographic 3 light-sensitive materials, in particular, color photographic papers.

However, in the case of using benzyl alcohol, diethylene glycol, triethylene glycol, alkanolamine, etc., becomes necessary as solvent since benzyl alcohol is low in water-solubility. However, the aforesaid compounds including benzyl alcohol give high BOD and COD, which are pollution loading values, and hence it is preferred for reducing pollution load to omit benzyl alcohol.

Furthermore, even when the aforesaid solvent is used, it takes a long time to dissolve benzyl alcohol and hence for reducing the work for the preparation of solution, it.is better not to use benzyl alcohol.

Also, when benzyl alcohol is carried in a bleach bath or blix bath, which is a post bath, it causes to form a leuco dye of cyan dye, which results in the reduction of color density. Furthermore, the washing out speed of developer components from light-sensitive materials is delayed, which sometimes give bad influences on the image storage stability of processed light-sensitive material. Accordingly, by the aforesaid reasons, it is preferred not to use benzyl alcohol.

In color development, it is general that the processing time is from 3 minutes to 4 minutes but recently, with the shortage of the time for delivery of finished aj^ i.l ~i :II5 lii19~ 4 products and the reduction of laboratory work, it has been desired to shorten the processing time.

However, when benzyl alcohol, which is a coloring accelerating agent, is removed and the processing time is shortened, the color density is, as a matter of course, reduced remarkably.

For solving this problem, various color development accelerating agents are proposed the compounds described in U.S. Patents 2,950,970, 2,515,147, 2,496,903, 2,304,925, 4,038,075, 4,119,462, British Patents 1,430,998, 1,455,413, Unexamined Published Japanese Patent Application Nos. 15831/78, 62450/80, 62451/80, 62452/80, 62453/80, Japanese Patent Publication Nos. 12422/76, and 49728/80) but the use of these compounds does not give sufficient color density.

Also, even when a method of incorporating 3-pyrazolidones is proposed the methods described in Unexamined Published Japanese Patent Application Nos. 26338/85, 158444/85, and 158446/85), there are disadvantages that the sensitivity is reduced and fog forms the light-sensitive materials are stored for a long time in unexposed state.

Furthermore, a method of incorporating color developing agents is proposed the methods described in U.S. Patents 3,719,492, 3,342,559, 3,342,597, Unexamined Published Japanese Pa-ent Application Nos. 6235/8'1, i 16133/81, 97531/82, 83565/82, etc.), but in this case, there occur disadvantages that the color development is delayed and fog forms, and hence such a method is not proper.

Also, various processes for processing reflectiontype silver halide color photographic light-sensitive materials using a color developer containing no benzyl alcohol or containing a greatly reduced amount of benzyl alcohol are proposed and are described, for example, in Unexamined Published Japanese Patent Application Nos. 20037/82, 48755/84, 174836/84, 177553/84, 26339/85, 172042/85, 31334/83, Japanese Patent Publication No. 29461/74, etc.

For the color photographic light-sensitive materials which are processed by the aforesaid color development process, anionic or nonionic surface active agents such as saponin; sulfosuccilnic acid; alkylbenzenesulfonic acids such as dodecylbenzenesulfonic acid, etc.; alkylnaphthalenesulfonic acid; sorbitansesquioleic acid esters; sorbitanmonolauric acid esters; alkylene oxide derivatives, etc., are used.

However, the use of such conventional surface active agent is insufficient for attaining the purpose of obtaining color photographs with the high maximum color density (Dmax) and the low minimum color density (Dmin), and with lees change in sensitivity and gradation by processing a color light-sensitive material with a color developer containing 6 substantially no benzyl alcohol in a very short period of time as within 2 minutes and 30 seconds.

Therefore, a first object of this invention is to provide a color image-forming process giving high color density in short period of time even by using a color developer containing substantially no benzyl alcohol.

A second object of this invention is to provide a color image-forming process giving less formation of fog and showing quick development.

A third object of this invention is to provide a color image-forming process giving less change in sensitivity and gradation.

[DISCLOSURE OF THE INVENTION] As the result of making various investigations for attaining the aforesaid objects, the inventors have discovered that in the case of processing a color photographic paper containing the specific fluorinated carbon-containing anionic surface active agent described hereinbelow in the silver halide emulsion layer thereof or a layer adjacent thereto, a high color density is obtained in short period of time even when a color developer containing substantially no benzyl alcohol is used and the present invention has been attained.

That is, the invention is a color image-forming process, which comprises processing, after exposure, a-si-lver J 7 halide color photographic light-sensitive material comprising a reflective support having provided thereon at least one silver halide emulsion layer and containing an anionic surface active agent having a fluorine-substituted aliphatic group having 4 to 18 carbon atoms as a hydrophobic group and -SO M or -OSO M (wherein M represents a hydrogen 3 3 atom or a cation) as a hydrophilic group in the molecule thereof in the emulsion layer or a layer adjacent thereto with a color developer containing substantially no benzyl alcohol in a time of up to 2 minutes and 30 seconds.

In this invention,, the term "containing substantially no benzyl alcohol" means that the concentration of benzyl alcohol in a developer is up to 0.5 ml/I Preferred examples of the aforesaid anionic surface active agent in this invention can be shown by the following general formula; (Rf) (B)m-X [I] n m wherein Rf represents a fluorine-substituted alkyl group having 4 to 18 carbon atoms or an alkenyl group, X represents -SO3M or -OSO 3 M (wherein M represnets a hydrogen atom or a cation), and B represents a di-valent or tri-valent organic residue such as a di-valent or tri-valent aliphatic hydrocarbon group an alkylene group or an alkylene VT 0' V-t) 'O nC ,,l/V 8 group in which the methylene is partially substituted by oxa), an arylene group phenylene, l,4-naphthylene, 2- 'hydroxy-1,4-naphthylene, etc.), and a di-valent heterocyclic group a di-valent benzimidazole group, 1-alkylenebenzimidazol-2-yl, etc.), said B also represents a poly-valent

R

group (SO0-N-Ro-CO) 2

R

2 -COOR -R 1 0-CO-R 1 CONH-R-, o SONR1-) formed by a combination of the divalent or tri-valent organic residue and a di-valent linkage group -NR-CO-, -CO-NR-, -S02 N wherein R is a hydrogen atom or an alkyl group having 1 to 18 carbon atoms).

In the above formula, R represents the aforesaid di-valent aliphatic hydrocarbon group, arylene group, or divalent heterocyclic group and 2 represents a tri-valent aliphatic hydrocarbon group.

o' Also, r represents an integet of 11jM 2 and m represents 0 or 1.

Then, some specific examples of the aforesaid anionic surface active agents particularly useful t this invention are shown below.

(A

CF

3

(C

2 7 So2 NCH 2 CH 2 CH2 So 3 Na

UC

3 77 (A 2) CF (CF 2) 7so 2N (CH 4SO K 3 7 2 24 3 (A 3) H( CF 2 6 CH 2 0( CH 2 )3s 3 SONa (A 4) H (CF 2 5 CH 2 0 (CH 2 3 so 3 SNa (A H (CF 2 10 CH 2 0ol 2 3 so 3 -N(qH 3 3 (A -6) CF 3 CF 2 )7s S 2 NCH 2 CH 2 0(CH 2

CH

2 0) n(C C2)3 so 3 Na

CI

u3H7 n= 1 (A 7) nlt- 3 (A 8) n (A 9) n (A CF 3 (CF 2 6 CONHCH 2 CH 2 O(l C 2 3 so 3 SNa (A 11) H(C 2 8 CON(CH 2 3 so 3 Na

C

3

H

7 (A 12 CH 2 COOCH 2 (CF 2 8

H

CHCOOCH 2(CF 2) 8H 2 2 8 ou3 13) CH 2COOCH 2(CF 2)6 CF3 CHCOOCH 2(F26c (A 14) HCO(CF 2 )6" so3 Na NHCO(CF 3 6 CF 3 SO Na 3 16.) N-(CF 2 6 CF 3 NaO sH 17) 7-(CF CF 3

N

NaO SCU (A -18)

(CF

2 6

H

O:~N C1 2 CH 2 O(CH 2 3 so 3 a (A 19) C H CH 2COOCH 2CH 2

NSO

2 (CF 2 7 C 17 3 CHCOOCH 2 CH 2NSO2 (CF 27C u3 DiCu3 (A iCF 3 (CF 2 7 /o3N (A 21) CF3( CF 2 7 so 3

K

(A 22) CF 3CF 2 1 CH2o3M (A -23) CF3( CF )6COO(CHt)3SO3 Na (A 4 C IS H. 3 '-CICOOCH 2 (CF 2 4

H

I0N~ 13 C 16

H

33 -ffHCOOCH 2 (CF 2 )6 CF 3 S 3 Na 26) NHCO( CF) 1

CF

2

OH

27) C 2 F 5 CF 3CF C CF-- (A -28) c 2 F 5

TF

3

CF

3 32 (A -29) cFCF CF CF-C C OCH 2CH 2OSO3 Na 22 3V These compounds which are %used in this invention can be synthezilted by the methods desq~ribed, for example, in U. S. Patents 2,559,715, 2,567,011, 2,732,398, 2,764,602, 2,806,866, 2,809,998, 2,915,376, 2,915,528, 2,934,450, 2,937,098, 2,957,031, 3,472,894, 3,555,089, Japanese Patent Publication No. 37304/70, Unexamined Published Japanese Patent Application No. 9613/72, J. Chem. Soc., page 2789(1950), ibid., pages 2574 znd 2640(1957), and J. Amer. Chem. Soc., Vol. 79, page 2549(1957).

A part of these fluorinated carbon-containing anionic surface± active agents for use in this invention Is commercially available as the trade name of Megafac F P-109, F-l10, F-115) from Dainippon In'k and Chemicals, Inc., or as the trade names of Monflor Monflor 31~) from Imperial Oiemical industry Co.

'khe fluorinated co~bon-containing anionic surface active agent for use in this ,n vention can be added to one or both of an oi1-solub-4, photoy raphic additive coupler, etc#) solution and aa' aqjueous colloid solution in the range such that solubility poxmits.

In this invention, oil drops contAining coupler can contain, a DIR colorlers col.pound-forming couplers, an ultraviolet ray absorbent, a discoloration inhibitor, a color stain preventiiin -_9,evt, a stain preventing agent, an antioxidant, etc.

The fluorine-substituted anionic surface active agent for use in this invention can be used singly or together with other surface active agent. It is sometimes more preferred to use the anionic surface active agent together with certain kind of surface active agent than the case of using the anionic surface active agent singly.

The fluorine-substituted anionic surface active agent for use in this invention can be used together with a so-called fluorine-unsubstituted anionic surface active agent and/or a nonionic surface active agent.

As the aforesaid fluorine-unsubstituted anionic surface active agent, the use of a compound having a hydrophobic group of 8 to 30 carbon atoms (hydrophobic group without being unsubstituted by fluorine) and -SO3M or -OSO 3

M

(M has the same significance as defined above about formula in one molecule thereof is preferred. These compounds are described in Ryohei Oda and Kazuhiro Teramura, Kaimen Kasseizai no Gosei to Ooyo (published by Maki Shoten) and A.W. Perry, Surface Active Agent, Interscience Publications- Inc., New York.

yAs the aforesaid nonionic surface active agent, the use of nonionic surface active agents described in Unexamined Published Japanese Patent Application No. 30933/73 and polyhydric alcohol fatty acid ester-series surface active agents is preferred. A polyhydric alcohol fatty acid esteri 16 series surface active agent having at least 2, preferably at least 3 hydroxy groups and also 6 to 25 carbon atoms of the fatty acid is preferred. Practically, the sorbitan fatty acid ester-series nonionic surface active agents described in U.S. Patent 3,676,141 are advantageously used in this invention.

Specific examples of the above-described fluorineunsubstituted anionic surface active agent are illustrated below.

(A 1 (A 2 (A 3 (A 4 (A 5 (A 6 C12H250SO Na C14H29GSO3Na Turkey Red Oil C12H25CONHCH2CH20SO3Na C2H25SO3Na C 12H 2SO Na C14H29SO3Na C H7 OCH 2

CH

2

OCH

2

CH

2

SO

3 Na (A 7) (A 8 (A 9) NaO3S-CH-COOC 8

H

1 7 CH2-COOC 8H17 C12H2 SONa C13H27CON SO3Na (A 10) el 17 (A 11) Ro Ro' Ro SONa 3

CH

In the above formula, Ro' represents -CH< 3

CH

3 3 In this invention; it-is particularly preferred to use at least one fluorine-substituted surface active agent for use in this invention together with at least one fluorine-unsubstituted anionic surface active agent having a hydrophobic group of 8 to 30 carbon atoms and -SO3M or

-OSO

3 M (M has the same significance as defined above about formula in one molecule thereof and/or at least one sorbitan fatty acid ester-series nonionic surface active agent.

In this invention, it is necessary that couplers are fused by heating or dissolved in organic solvent to form a liquid thereof before the emulsification thereof. In this case, however-,-the coupler which can be directly emulsified by fusing it is limited to a compound having melting point of up to about As an organic solvent (so-called oil) which is used for finely dispersing a coupler in an aqueous medium, an organic solvent which is substantially insoluble in water a0 18 and has a boiling point of at least 190 0 C at atmospheric pressure is useful. .Such an organic solvent can be selected from carboxylic acid esters, phosphoric acid esters, carboxylic acid amides, ethers, and substituted hydrocarbons.

Specif.c examples thereof are di-n-butyl phthalic acid ester, diisooctyl phthalic acid ester, dimethoxyethyl phthalic acid esters, di-n-butyl adipic acid ester, diisooctylazelaic acid ester, tri-n-butyl phthalic acid ester, butyl lauric acid ester, di-n-sebacic acid ester, tricresyl phosphoric acid ester, tri-n-butylphosphoric acid ester, triisooctyl phosphoric acid ester, N,N-diethylcaprylic amide, N,N-dimethylpalmitic amide, n-butyl-m-pentadecyl phenyl ether, ethyl-2,4-tert-butyl phenyl ether, chlorinated paraffin, etc.

In this invention, it is sometimes advantageous to use a low-boiling solvent (having boiling point of up to 130 0 C at room pressure) or a water-soluble high-boiling solvent together with the aforesaid solvent for dissolving couplers. For example, there are propylene carbonate, ethyl acetate, butyl- acetate, ethyl propionic acid ester, sec- I butyl alcohol, tetrahydrofuran, cyclohexanone, dimethylformamide, diethyl sulfoxide, methylcllosolve, etc.

As an emulsification apparatus which is used for the practice of this invention, an apparatus giving large shearing force to processing liquid or an apparatus giving L i 19 high-1ntensity ultrasonic energy thereto is suitable. In partictlar, a colloid mill, a 'homogenizer, a capillary type emulsification apparatus, or an emulsification apparatus having a liquid siren, an electromagnetostrain type ultrasonic generator, or Poleman horn gives good results.

As the photographic layer containing the fluorinesubstituted anionic surface active agent for use in this invention, a silver halide emulsion layer and/or an adjacent layer thereto is preferred, and a silver halide emulsion layer is particularly preferred.

The amount of the, fluorine-substituted anionic surface active agent for use this invention depends upon the kind of couplers, the kind of other additives, the kind and amount of dispersing solvent, as the case may be, the kind and amount. of other surface active agent(s), etc., but is generally fromn 0.2 to 50% by weight of a dispersion a solution *formed by dispersing a coupler and other oilsoluble photographic additive(s) in a dispersing medium) 1 j F As substances which can exist together with couplers, there are oil-soluble photographic additives such as discoloration inhibitor, ultraviolet ray absorbents, DIR couplers, antioxidant, etc.

The "reflective support" for use in this invention is a support having high reflectivity for clearly viewing color images formed in silver~ halide emulsion layer(s) and L_ such a reflective support includes a support coated with a hydrophobic resin having dispersed therein a light-reflecting substance such as titanium oxide, zinc oxide, calcium carbonate, calcium sulfate, etc., or a support composed of a hydrophobic resin having dispersed therein the light-reflective substance. For example, there are baryta papers, polyethylene-coated paper, polypropylene-series synthetic papers, and transparent supports such as glass plates, polyester films, polyethylene terephthalate films, cellulose triacetate films, cellulose nitrate films, etc., polyamide films, polycarbonate films, polystyrene films, etc., having provided thereon a reflective layer or having a reflective substance. The support can be properly selected from these supports according to the purposes.

Then, processing steps (image-forming step) of this invention are explained.

In the color development processing step in this invention, the processing time is as short as up to 2 minutes and 30 seconds. A preferred processing time is from 30 seconds to 2 minutes. In this case, the processing time means a period from the time at which a light-sensitive material is brought into contact with a color developer to the time of the light-sensitive material coming into contact with a next bath and includes the time for transporting the light-sensitive material from the color development bath to i the next bath.

A color developer for use in the development process of this invention is preferably an alkaline aqueous solution containing an aromatic primary amine-series color developing agent as the main component. As the color developing agent, p-phenylenediamine-series compounds are preferably used and typical examples thereof include 3-methyl-4-amino-N,N-Oiethylaniline, 3-methyl-4-amino-N-ethyl-N- -hydroxyethylaniline, 3-methyl-4-amino-N-ethyl-N--mnethanesulfonamidoethylaniline, 3-methyl-4-amino-N-ethyl-N- -methoxyethylaniline and the sulfates, hydrochlorides, phosphates, or p-toluenesulfonates thereof, tetraphenylborates, p-(t-octyl)benzenesulfonates, etc. Of these compounds, 3-methyl-4-amino-N-ethyl-N-8-methanesulfonamidoethylaniline and the salts thereof are particularly preferred.

Aminophenolic derivatives include o-aminophenol, paminophenol, 4-amino-2-methylphernol, 2-amino-3-methylphenol, 2-oxy-3-amino-l,4-dimethylbenzene, etc.

Other color developing agents described in L.F.A.

Mason, Photographic Processing Chemistry, pages 226-229, Focal Press, U.S. Patents 2,193,015, 2,592,364 Unexamined Published Japanese Patent Application No. 64933/73, etc., can be also used. If necessary, two or more kinds of color developing agents may be used as a combination thereof.

The processing temperature of the color developer in L

WWWWWWE

3 22 this invention is preferably from 30°C to 50°C, and more preferably from 33 0 C to Also, as development accelerators, various compounds substantially excluding benzyl alcohol may be used. Examples thereof are various kinds of pyrimidium compounds and other cationic compounds described in U.S. Patent 2,648,604, Japanese Patent Publication No. 9503/69, and U S. Patent 3,171,247, cationic dyes such as phenosafranine, neutral salts such as thallium nitrate and potassium nitrate, polyethylene glycol and the derivatives thereof described in Japanese Patent Publication No. 9304/69, U.S. Patents 2,533,990, 2,531,832, 2,950,970, and 2,577,127, nonionic compounds such as polythioethqrs, etc., thioether-b.jries compounds described in U.S. Patent 3,201,242, and other compounds described in Unexamined Published Japarase Patent Application Nos. 156934/73 and 220344/85.

Also, in the short time development process as in this invention, not only the means for accelerating development but also a technique for preventing the formation of development fog becomes important. As an antifoggant in this invention, an alkali metal halide such as potassium bromide, sodium bromide or potassium iodide, and also an organic antifoggant are preferred. As organic antifoggants, there are, for example, nitrogen-containing heterocyclic compound such as benzotriazole, 6-nitrobenzimidazole, flitroisoindazole, 5-rnethylbenzotriazole, ole, 5-chlorobenzotriazole, 2-thiazolylbenzimidazole, 2-thiazolylmethylbenzimidazole or hydroxyazaindrizine, mercaptosubstituted heterocyclic compounds such as captotetrazole, 2-niercaptobenzimidazole or 2-mercaptobenzothiazole, and further rercapto-substituted aromatic compounds such as thiosalicylic acid. Of these compounds, halides are particularly preferred. The antifoggant may be accumulated in the color developer by dissolving out form color light-sensitive materials during processing.

Furthermore, the color developer in this invention may contain a pH btiffer such as carbonatesf borates, or phosphates of an alkali metal; a preservativye such as hydroxylaznine, tri ethanolamnine, compounds described in West German Patent Application (OLS) No. 2,622,950, su~lfites, and bisulfites; an organic solvent such as diethylene glycol; a dye-torming couplet; a tomrpetifig coupler; a nucleating agent such as sodiumboron hydride; an auxiliary developing agent such as I-phenyl-3-pyrazolidone; a tackifier; an aminopolycarboxylic acid such as ethylenediaminetetraacetic acid* ni trilotriacatic acid, cyclohexanrndiaminetetraaoetic acid, imirnodiacetic ai, N-hydroxymethyl ethy~ened iamnetri acetic acid, diethylenetriaminepentaacetic acid, or triethylehetetraminehexaacetic acid: an organic phosphonic acid. such as l-hydroxyethylidene-l,J)-diphosphonic acid or those de-

~N

24 scribed in Research Disclosure, No. 18170 (May, 1979); an arninophosphonic acid such as aminotris(methylenephosphonic acid) ethyl enedi amine-N,N, N' N'-tetramethylenephospbonic acid, etc. and a chelating agent such as phosphonocarboxylic acids, etc., described in Unexamined Published Japanese kit Patent Application Nos. 102726/77f 42730/78, 121127/79, 4024/80, 4025/80, 126241/80, 65955/80, 65956/80, and Research Disclosure, No. 18170 (May, 1979).

Also, i~f necessary, the color development bath is composed of two or more baths and a replenisher for color developer is supplied from the first bath or the last bath for practicing the shortago of the development time and reduction of the amount of the replenisher.

A silver halide color light-sensitive material is usually bleached after color development. The bleach f process may be performed simultaneously with fix process (blix) or separately With fix process. As a bleaching agent, for example, compounds of Multivalent metals such as iron(IXI)O cobalt(IXI), chrorniurn(VI), copper(II)l etc*, peracids, quinones, nitroso compoondso etc., are used, Examnples thereof include a ferricyanides, dichrornates, or" ganic complex salts of iron(iII) or cobalt(I~I) aminopolycarboxylic acids, such as othylenediaminetetraacetic, acid, diethylenetriaminepent44cetic acid, nitrilotriacetic acid, l,3-dianiino-2-propanoltetraacetic acid, etc., oomplex salts of organic acid such as citric acid, tartaric acid, malic acid, etc., persulfates, manganates, nitrosophenol, etc. Of these substances, potassium ferricyanide, sodium ethylenediaminetetraacetato ferrate, ammonium ethylenediaminetetraacetato ferrate, ammonium triethylei.atetraminepent acetato ferrate, and persulfates are particularly useful. Ethylene.

diaminetetraacetic acid iron(III) complex salt is useful in an independent bleach solution and in a monobath blix solution.

Also, the bleach solution or blix solution may, if necessary, contain various kinds of accessorators. For example, bromine ion, iodine ion, as well as thiourea-series compounds as shown in U.S. Patent 3,706,561, Japanese Patent Publication Nos. 8506/70, 26586/74, Unexamined Published Japanese Patent Application Nos. 32735/78, 36233/78, and 37016/78 thio--series compounds shown in Unexamined Published Japanese Patent Application Nos. 124424/78, 95631/78, 57831/78, 32736/78, 65732/78, 52534/79, and U.S. Patent 3,893,858, hetercyclic compounds described in Unexamined Published Japanese Patent Application Nos. 59644/74, •I 140129/75, 28426/78, 141623/78, 104232/78, 35727/79, etc., thioether-series compounds described in Unexamined Published Japanese Patent Application Nos. 20832/77, 25064/80, 26506/80, etc., quaternary amines described in Unexamined Published Japanese Patent Application No. 84440/73, and 26 thiocarbamoyls described in Unexamined Published Japanese Patent Application No. 42349/74 may be used.

As a fixing agent, there are thiosulfates, thiocyanates, thioether-series compounds, thiou a large amount of iodide, etc., but thiosulfates are generally used. As a preservative for the blix solution or the fix solution, sulfites, bisulfites, or carbonyl-bisulfite adducts are preferred.

After blix process or fix process, wash process is usually performed. For the wash step, various known compounds ma be used for preventing precipitation or saving waters Examples of these compounds are a water softener for preventing precipitation, such as inorganic phosphoric acids, aminopolycarboxylic acid, organic phosphoric acids, etc., antibacterial agents or antifungal agents for preventing the generation of various bacteria, algae, and molds, a hardening agent represented by magnesium salts or aluminum salts, a surface active agent for reducing drying load and preventing the occurrence of uneven drying, etc. Furthermore, the compounds described in L.E. West, Photographic Science and Engineering, Vol. 9, No. 6 (1965), etc., may be added to wash water. In particular, the addition of chelating agents and antifungal agents is effective.

Also, by employing a multistage 2 to stages) countercurrent system for the wash step, the amount ;6r 27 of water can be saved.

Also, after or in place of a wash step, a multistage countercurrent stabilization process as described in Unexamined Published Japanese Patent Application No. 8543/82 may be used. In this process, 2 to 9 countercurrent tanks are necessary. The stabilization solution may contain various compounds for stabilizing images. For example, there are buffers for adjusting the pH of photographic layers borates, ntetaborates, borax, phosphates, carbonates, potassium hydroxide, sodium hydroxide, aqueous ammonia, monocarboxylic acid, dicarboxylic acid, polycarboxylic acid, etc.) or formalin. Furthermore, if necessary, water softeners inorganic phosphoric acids, aminopolycarboxylic acids, organic phosphoric acids, aminopolyphosphonic acids, phosphonocarboxylic acids, etc.), germicides Proxel, isothiazolone, 4-thiazolylbenzimidazole, halogenated phenolbenzotriazole, etc.), surface active agents, brightening agents, hardening agents, etc., may be added thereto.

Also, as a layer pH controlling agent after processing, various ammonium salts such as ammonium chloride, ammonium nitrate, ammonium sulfate, ammonium phosphate, ammonium sulfite, ammonium thiosulfate, etc., can be added thereto, It is preferred that couplers incorporated into light-sensitive materials are rendered non-diffusible by 1

A

)bic 1 ^"ri v 28 having a ballast group or being polymerized. Furthermore: 2-equivalent color couplers the coupling active position of which is substituted by a releasing group is more effective for reducing the amount of silver coated than the case of using 4-equivalent color couplers having a hydrogen atom at the coupling active position thereof. Couplers providing colored dyes having a proper diffusibility, colorless compound-forming coi[lers, DIR couplers releasing a development inhibitor with the coupling reaction or couplers releasing a development accelerator with the coupling reaction thereof can be used.

Typical examples of the yellow couplers which can be used in this invention are oil-protect type acylacetamideseries couplers. Specific examples thereof are described in U,S. Patents 2,407,210, 2,875,057, 3,265,506, etc.

In this invention, 2-equivalent yellow couplers are preferably used and typical examples thereof are oxygen atom-releasing type yellow couplers described in U.S. Patents 3,408,194, 3,447,928, 3,933,501, 4,022,620, etc., or nitrogen atom-releasing type yellow couplers described in p Japanese Patent Publication No. 107:39/83, U.S. Patents 4,401,752 and 4,326,024, RD 18053 (April, 1979), British Patent 1,425,020, West German Patent Application (OLS) Nos.

2,219,917, 2,261,361, 2,329,587, 2,433,812, etc. of these couplers, a-pivaloylacetanilide-series couplers are excel- 29 lent in fastness, in particular light fastness of the colored dyes formed, while a-benzoylacetanilide-series couplers give high color density.

As magenta couplers which can be used in this invention, there are oil-protect type indazolone-series or cyanoacetyl-series couplers, preferably couplers and pyrazoloazole-series couplers such as pyrazolotriazoles, etc. The 5-pyrazolone-series couplers the 3position of which is substituted by an arylamino group or an acylamino group are preferred in the viewpoints of the hue and color density of colored dyes and typical examples thereof are described in U.S. Patents 2,311,082, 2,343,703, j 2,600,788, 2,908,573, 3,062,653, 3,152,896, 3,936,015, etc.

Preferred releasing groups for the 2-equivalent olone-series couplers include nitrogen atom-releasing groups described in U.S. Patent 4,310,619 and arylthio groups described in U.S. Patent 4,351,897. Also, couplers having a ballast group described in European Patent 73,636 give high color density.

Pyrazoloazole-series magenta couplers include pyrazolobenzimidazoles described in U.S. Patent 3,369,879, preferably pyrazolo[5,l-c]Cl,2,4]triazoles described in U.S.

Patent 3,725,067, pyrazolotetrazoles described in Research DiTclosure, No. 24220 (June, 1984), and pyrazolopyrazoles described in Research Disclosure, No. 24230 (June, 1984).

1^t'' ,t A js i 1 \i From the viewpoints of less yellow side absorption of colored dyes and high light fastness of colored dyes, imidazo- [1,2-bJpyrazoles described in European Patent 119,741 are preferred and pyrazolo[l,5-b][1,2,4]triazole described in European Patent 119,860 is particularly preferred.

Cyan couplers for use in this invention include oilprotect type naphthoic and phenolic couplers.

As typical naphthoic cyan couplers, there are naphthoic couplers described in U.S. Patent 2,474,293 and, preferably oxygen atom-releasing type 2-equivalent naphthoic couplers described ih U.S. Patents 4,052,212, 4,146,396, 4,228,233, and 4,296,200. Also, specific examples of the phenolic couplers are described in U.S. Patents 2,369,929, 2,801,171, 2,772,162, 2,895,826, etc. Cyan couplers having high fastness to moisture and heat are preferably used in this invention, and typical examples there are the phenolic cyan couplers having an alkyl group of at least two carbon atoms at the meta-position of the phenol nucleus described in U.S. Patent 3,772,002, 2,5-diacylamino-substituted phenolic couplers described in U.S. Patents 2,772,162, 3,758,308, S4,126,396, 4,334,011, and 4,327,173, West German Patent Application (OLS) No. 3,329,729, Unexamined Published Japanese Patent Application No. 166956/84, etc., and phenolic couplers having a phenylureido group at the 2-position thereof and an acylamino group at the 5-position thereof S31 described in U.S. Patents 3,446,622, 4,333,999, 4,451,559, 4,427,769, etc.

In this invention, the graininess of the color images formed can be improved by using a coupler giving colored dye having a proper diffusibility together with the aforesaid coupler(s). About such couplers giving diffusible dyes, specific examples of the magenta couplers are described in U.S. Patent 4,366,237 and British Patent 2,125,570 and specific examples of the yellow, magenta and cyan couplers are described in European Patent 96,570 and West German Patent Application (OLS) No. 3,234,533.

The dye-forming couplers and the specific couplers described above may form a dimer or higher polymer. Typical examples of the polymerized dye-forming couplers are described in U.S. Patents 3,451,820 and 4,080,211. Also, specific examples of the polymerized magenta couplers are described in British Patent 2,102,173 and U.S. Patent 4,367,282.

The couplers for use in this invention can be used for one light-sensitive layer as a mixture of two or more Sfor meeting the properties required for the light-sensitive materials or the same kind of coupler may be incorporated in two or more light-sensitive layer.

A standard amount of a color coupler is in the range of from 0.001 mol to 1 mol per mol of the light-sensitive f silver halide, with from 0.01 mol to 0.5 mol of a yellow coupler, from 0.003 mol to 0.3 mol of a magenta coupler, and from 0.002 mol to 0.3 mol of a cyan coupler, per mol of the light-sensitive silver halide being preferred.

The light-sensitive materials for use in this invention may further contain hydroquinone derivatives, aminophenol derivatives, amines, gallic acid derivatives, eatechol derivatives, ascorbic acid derivatives, colorless compound-forming couplers, sulfoamidophenol derivatives, etc., as color fog preventing agents or color stain preventing agents.

Also, the light-sensitive materials for use in this invention can further contain known discoloration inhibitors, Typical examples of organic discoloration inhibitors are hydroquinones, 6-hydroxychromans, spirochromans, p-alkoxyphenols, hindered phenols comprising bisphenols, gallic acid derivatives, methylenedioxybenzenes, aminophenols, hindered amines and the ether or ester derivatives of the aforesaid compounds formed by silylating or alkylating the phenolic hydroxy group of these compounds.

Also metal complexes represented by (bissalicylaldoxymato)nickel complex and (bis-N,N-dialkyldithiocarbamato)nickel complex, etc. can also be used.

For preventing the deterioration of yellow dye images by heat, moisture, and light, the compound having

L

-wr~---rrrrr~~i- 33 both moieties of hindered amine and hindered phenol in one molecule as described in U.S. Patent 4,268,593 gives good results. Also, for preventing the deterioration of magenta dye image, particularly by light, spiroindans described in Unexamined Published Japanese' Patent Application No.

159644/81 and chromans substituted by hydroquinone diether or hydroquinone monoether described in Unexamined Published Japanese Patent Application No. 89835/80 give preferred results.

For improving the storage stability, in particular, the light fastness of cyan images, it is preferred to use a benzotriazole-series ultraviolet ray absorbent with the cyan coupler(s). The ultraviolet ray absorbent may be coemulsified with the cyan coupler(s).

The ultraviolet ray absorbent is desirably used in an amount sufficient for imparting light stability to cyan dye images but since if the amount is too much, the unexposed portions (background portions) of the color photographic light-sensitive material are sometimes yellowed, the amount thereof is usually selected in the range of from 1 x 10 4 mol/m 2 to 2 x 10 mol/m 2 particularly from x 10 4 mol/m 2 to 1.5 x 10 3 mol/m 2 In the light-sensitive layer structure of an ordinary color photographic paper, the ultraviolet ray absorbent(s) are incorporated in either one of both layers L l

I

34 adjacent to or, preferably, in both layers adjacent to a red-sensitive emulsion layer containing cyan coupler. When the ultraviolet ray absorbent(s) are incorporated in the interlayer between a green-sensitive layer and a red-'sensitive layer, they may be emulsified together with a color stain preventing agent. When the ultraviolet ray absorbent(s) are incorporated in a protective layer, another protective layer may be formed on the protective layer as the outermost layer, The outermost protective layer may contain a matting agent having a proper particle size.

The light-sensitive materials which are processed in this invention can contain ultraviolet ray absorbents in the hydrophilic colloid layers.

The light-sensitive materials which are processed in this invention may further contain water-soluble dyes in the hydrophilic colloid layers as filter dyes or for the purpose of irradiation or halation prevention.

The light-sensitive materials which are processed in this invention may further contain whitening agents such as stilbene-series, triazine-series, oxazole-series, or cou- Smarin-series whitening agents in the photographic emulsion layers or other hydrophilic colloid layers. The whitening agent may be water-soluble or a water-insoluble whitening agent may be used in the form of the dispersion.

The light-sensitive materials for use in this inven- I Ovo 's tion, as described above, can be applied to a multilayer multicolor photographic material having at st two emull.

sion layers each having different spectral nsitivity on a support. A multilayer natural color photographic material usually has at least one red-sensitive emulsion layer, at least one green-sensitive emulsion layer, and at least one blue-sensitive emulsion layer on a support. The disposition order of the layers can be optionally selected according to the purposes. Also, each of the aforesaid emulsion layers may be composed of two or more emulsion layers each having different sensitivity or a light-insensitive layer may exist between two or more emulsion layers each having the same sensitivity.

The light-sensitive material for use in this invention preferably has auxiliary layers such as protective layer(s), interlayers, a filter layer, an antihalation layer, a back layer, etc., in addition to the silver halide emulsion layers.

As a binder or protective colloid which can be used for the emulsion layers and interlayers of the light-sensitive materials for use in this invention, gelatin is advantageously used but other hydrophilic colloids can be used.

Examples of the binders or protective colloids are proteins such as gelatin derivatives, graft polymers of /4 r 1 L 36 gelatin and other polymers, albumin, casein, etc.; cellulose derivatives such as hydroxyethyl cellulose, carboxymethyl cellulose, cellulose sulfuric acid ester, etc.; saccharose derivatives such as sodium alginate, starch derivatives, etc.; and synthetic hydrophilic polymeric substances such as homopolymers or copolymers such as polyvinyl alcohol, polyvinyl alcohol partial acetal, poly-N-vinylpyrrolidone, polyacrylic acid, polymethacrylic acid, polyacrylamide, polyvinylimidazole, polyvinylpyrazole, etc.

As gelatin lime-processed gelatin as well as acidprocessed gelatin and enzyme-processed g.tatin as described in Bull. Soc. Sci. Phot. Japan, No, 16, p. 30(1966) can be used. Furthermore, the hydrolyzed product or enzyme-decomposed product of gelatin can be used.

The light-sensitive materials in this invention may further contain various stabilizers, stain preventing agents, developing agents or the precursors thereof, development accelerators or the precursors thereof, lubricants, mordants, matting agents, antistatic agents, plasticizers, or other additives useful for the photographic light-sensitive materials in addition to the above-described additives.

Typical examples of such additive are described in Research Disclosure, 17643 (December, 1978) and ibid,, 18716 (November, 1979).

Xn this invenhion, silver chlorobromide, silver i _XI I chloride, silver chloroiodobromide, silver bromide, silver iodobromide, etc., are used as a silver halide, but silver bromide, silver chlorobromide and silver chloride each containing substantially no silver iodide are preferred, and silver chloribromide containing 20 to 98 mol% of silver bromide is more preferred. Also, for the purpose of processing a far short time, the use of silver chloride or silver chlorobromide containing at least 90 mol%, in particular, at least 95% silver chloride is preferred.

The silver halide grains for use in this invention may have different phase between the inside and the surface layer thereof, may be a multiphase structure having a junction structure, or may be composed of a uniform phase throughout the whole grain. Also, the silver halide grains may be composed of a mixture thereof.

The average grain size (shown by the diameter of the grains when the grain is spherical or similar to spherical, and shown by the average value based on the projected area using, in the case of cubic grains, the edge length as the grain size) of the silver halide grains for use in this invention is preferably in the range of from 0.1 p to 2 p, particularly preferably from 0.15 p to 1 p. The grain size distribution may be narrow or broad but the use of so-called monodispersed silver halide emulsion, wherein the value (coefficient of variation) obtained by dividing the standard

A,

i 1 1 deviation in the grain size distribution curve of the silver halide emulsion by the average grain size of the silver halide grains in the emulsion is within 20%, particularly preferably within 15%, is preferred. Also, for satisfying the desired gradation for the light-sensitive material, in the emulsion layers each having substantially the same color sensitivity, two or more kinds of monodispersed silver halide emulsions (preferably having the above-described coefficient of variation) each having different grain size can be used as a mixture thereof for _ne emulsion layer or can be used as separate emulsion layers. Furthermore, two or more kinds of polydispersed silver halide emulsion layers or a combination of the monodispersed silver halide emulsion and a polydispersed silver halide emulsion can be used as a mixture thereof for one emulsion layer or can be used as separate emulsion layers.

The silver halide grains for use in this invention may have a regular crystal form such as cube, octahedron, dodecahedron, tetradecahedron, etc., an irregular cryetal form such as sphere, etc.. or a composite form of these crystal forms. However, silver halide grains having a regular crystal form such as cube and tetradecahedron are preferred. Also, the silver halido grains may be tabular grains and in this case, an emulsion wherein tabular grains of at least 5, in particular at least 0 in the ratio of

L_

39 length/thickness account for at least 50% of the total projected area of the grains can ba used in this invention.

An emulsion.containing a mixture of various silver halide grains having different crystal form may be also used. The emulsion may be of a surface latent image type of forming latent images mainly on the surface thereof or of an internal latent inge type of forming latent images mainly in the inside of the grains although the former type is preferred.

The photographic emulsions which are used for the light-sensitive materials processed according to this invent!on can be prepared by the methods described in P.

Glafkides, Chimie et Physique Photograp'!1 e, published by Paul Montel. 1967); G.F. Duffin, Ph Ia~phic Emulsion Chemistry, published by Focal Press, and V.L.

Zelikman et al., Making and Coating PhoV hic Emulsion, published'by Focal Press, (1964), etc. Th.. is, the emulsion car be prepared by an acid method, a neutral method, an ammonia method, etc., and as a method of reacting a soluble silver salt and a soluble halide, a single jet method, a double jet method, a combination thereof, etc., may be employed. A method (so-called reverse mixing method) of forming grains in the existence of excess silver ions can also be used. As o.a system of the double jet method, a method of keeping pAg constant in a liquid phase of forming i lit a silver halide, so-called controlled double jet method, can also be used. According to the method, a silver halide emulsion containing grains having a regular crystal form and approximately uniform grain sizes can be obtained.

Furthermore, an emulsion prepared by a so-called conversion method including a step of converting a silver halide alriady formed before finishing the formation of the silver halide grains into a silver halide having small solubility product or an emulsion to which the similar halogen conversion was applied after finishing the formation of the silver halide grains can also be used in this invention.

During the formation or physical ripening of the silver halide grains, P cadmium salt, a zinc salt, a thallium salt, an iridium salt or the complex salt thereof, a rhodium salt or the complex salt thereof, an iron salt or the complex salt thereof, etc., may exist in the system.

The silver halide emulsions are, after the formation of the silver halide grains, usually physically ripened, desalted, and chemically ripened before coating.

A known silver halide solvent ammonia, Spotassium rhodanate, or thioethers and thione compounds described in U.S. Patent 3,271,157, Unexamined Published Japanese Patent Application Nos. 12360/76, 83408/78, 144319/78, 100717/79, 155828/79, etc.) can be used for the precipitation, physical ripening, and chemical ripening.

41 For removing soluble silver salts from emulsions after physical ripening, a noodle washing method, a flocculation sedimentation method, an ultrafiltration method, etc. can be employed.

The silver halide emulsions which are used for the light-sensitive materials to be processed in this invention can be chemically sensitized by a sulfur sensitization method using active gelatin or a sulfur-containing compound capable of reacting with silver thiosulfates, thioureas, mercapto compounds, or rhodanines); a reduction sensitization method using a reducing substance stannous salts, amines, hydrazine derivatives, fortamidinesulfinic acid, or silane compounds); a noble metal sensitization method using a metal compound gold complex salts and complex salts of metal belonging to group VIII of the Periodic Table, such as Pt, Ir, Pd, Rh, fe, etc.), a combination thereof, etc.

Of the aforesaid chemical sensitizations, independent use of the sulfur sensitization is more preferred.

Each of the blue-sensitive, green-sensitive and red- Ssensitive emulsions for the color light-sensitive material for use in this invention is spectrally sensitized by a methine dye, etc., such that the emulsion has each color sensitivity. The dyes for use include cyanine dyes, merocyanine dyes, complex cyanine dyes, complex merocyanine f II i

N.^

L 42 dyes, holopolar cyanine dyes, hemicyanine dyes, styryl dyes, and hemioxonol dyes. Particularly useful dyes are dyes belonging to cyanine dyes, merocyanine dyes, and complex merocyanine dyes.

For these dyes can be applied nuclei usually utilized for cyanine dyes as basic heterocyclic nuclei.

That is, pyrroline nuclei, oxazoline nuclei, thiazoline nuclei, pyrrole nuclei, oxazole nuc. ei, thiazole nuclei, selenazole nuclei, imidazole nuclei, tetrazole nuclei, pyridine nuclei, etc.; the nuclei formed by fusing an alicyclic hydrocarbon ring to the aforesaid nuclei, and the nuclei formed by fusing an aromatic hydrocarbon ring to the aforesaid nuclei, such as indolenine nuclei, benzindolenine nuclei, indole nuclei, benzoxazole nuclei, naphthoxazole nuclei, benzothiazole nuclei, naphthothiazole nuclei, benzoselenazole nuclei, benzimidazole nuclei, quinoline nuclei, etc., can be applied for the dyes described above. These nuclei may be substituted on carbon atoms.

For merocyanine dyes or complex merocyanine dyes may be applied 5-membered or 6-membered heterocyclic nuclei such as pyrazolin-5-one nuclei, thiohydantoin nuclei, 2-thiooxazolidine-2,4-dione nuclei, thiazolidine-2,4-dione nuclei, rhdanine nuclei, thiobarbituric acid nuclei, etc., as a nucleus having a ketomethylene structure.

These sensitizing dyes may be used singly or as a r, combination thereof. A combination of sensitizing dyes is 1* frequently used for the purpose of supersensitization.

Typical examples of the combinations are described in U.S.

Patents 2,688,545, 2,977,229, 3,397,060, 3,522,052, 3,527,641, 3,617,293, 3,628,964, 3,666,480, 3,672,898, 3,679,428, 3,703,377, 3,769,301, 3,814,609, 3,837,862, and 4,026,707, British Patents 1,344,281 and 1,507,803, Japanese Patent Publication Nos. 4936/68 and 12375/78, and Unexamined Published Japanese Patent Application Nos. 110618/77, 109925/77.

The emulsion may contain a dye having no spectrally sensitizing activity by itself. or a substance which does ilot substantially absorb visible light and shows supersensitizing activity together with the sensitizing dye(s).

[BEST MODE FOR CAR~RYING OUT THE INVENTION] Then, the invention is explained in detail by the examples but the invention is not limited thereto.

EXAMPLE 1.

To 24.0 g of yellow !,,oupler (Y 1) were added 35 ml of ethyl acetate and 12 ml of dibutyl phthalate as a solvent I, to dissolve the coupler, the solution was added to 160 ml of an aqueous 12% gelatin solution containing 10 ml of an aqueous solution of lo% Comparison Compound~ R 1 (sodium dibutylenesulfonate) as a dispersing agent, and2 the mixture was emulsified by means of a high-speed stirrer.

44 A whole amount of the emulsified dispersion was added to a silver chlorobromide emulsion (containing 70 g/kg of Ag) containing 80% of Br, the mixture was coated on a paper support, both surfaces of which had been laminated with polyethylene, such that the coated amount of silver became 0.31 g/m 2 and then a gelatin layer was formed on the emulsion layer to provide Comparison Sample Then, Samples to were prepared as follows.

Sample (B) Same sample as Sample except that 1.0 g of Compound A 1 of this invention was used in place of R 1 as a dispersing agent.

Sample (C) Same sample as Sample except that 1.0 g of Compound A 9 of this invention was used in place of R 1 as a dispersing agent.

Sample (D) Same sample as Sample except that 1.0 g of Compound A 11 of this invention was used in place of R 1 as a dispersing agent.

Sample (E) Same sample as Sample except that 1.0 g of Compound A 20 of this invention was used in place of R 1 as a dispersing agent.

Sample (F) Same sample as Sample except that 1.0 g of Compound A 26 of this invention was used in place of R 1 as a dispersing agent.

Furthermore, Samples to and Samples to were, respectively, prepared by using magenta coupler (M 1) and cyan coupler (C respectively, in place of the yellow coupler (Y 1) in Samples to In addition, in the case of using the magenta cou- 2 pler, the coated amount of the coupler was 0.37 g/m 2 the coated amount of the silver chlorobromide emulsion containing 75 mol% of Br was 0.20 g/m 2 as silver and in the case of using the cyan coupler, the coated amount of the coupler was 2 0.33 g/m and the coated amount of the silver chlorobromide emulsion containing 70 mol% Br was 0.28 g/m 2 as silver.

s 1 1 V y-1 0-C-COHONH-/ CH3 0 Ca HCO0(CH 2 3 0/02 C 5

H

1 (t) I 11 (t) 802

OH

m 1 00C

CH

3 0 8 1

X\

lT )NH

\C;

8

H:

N H S 0

L,

C 1 0 2

HS

NHCOGHO C 5

H

1 (t) 0 5

H

1 (t)

CHCH

2 Comparison Compound R-l

C

4

H

9 These samples were subjected to stepwise exposure for sensitometry and then processed by Process A or Process B using Color Developer or as described below, respectively. Process A differs from Process B by the difference in content between Color Developers and (B) and other contents are same in both processes.

k V -F ruu~ (Processing step) (Temperature) Development 38 0

C

Bi ix 330C Wash 28 to 35 0

C

(Composition of Developer) color Developer Diethylenetriaminepentaacetic acid SNa Salt Benzyl Alcohol Diethylene Glycol Na2 so 3 KBr Hydroxylamine Sulfate 4-Amino-3-inethyl-N-ethyl-N-[6 (methanel,,ulfonamido) ethyl] -pphenylenediamine *Sulfate Na 2 CO 3 (monohydrate) B 'rightening Agent (stiltbeneseries) Water to make1 (pH 1' Color Developer Di ethyl enetriaminepentaacetic acid Salt Na 250 KBr H-ydroxylamine Su~lfate (Time) 2. 0 1m.

1.5 mim.

3.0 min.

2.0 g 15 ml 10 mal 2.0 g 0.5 g 3.0 g 5.0 g 30.0 g 1.0 g I000 0.1) 2.0 g 2.0 g 0.5 g 3,0 g I A 4

,T

4 -Amino- 3 -methyl-N-ethyl-N- [0 (nmethanesul fonamido) ethyl]-pphenylenediamine .Sulfate Na 2Co3 (monohydrate) Brightening Agent (stilbeneseries) Water to make (Blix Solution Composition) Ammnoniumn Thiosulfate '(54 wt.%) Na 2so3 NH 4 Fe(III) (EDTA)J EDTA -2Na Water to make 5.0 g 30.0 g 1.0 g 1,000 ml PH 10.1) 150 4 1,000 (pH 6.i9) The evaluation of the photographic properties was performed on two items of maximum density (Dmax) and minimum density (Dmin). The results are shown in Table 1.

_r l Table 1 1 1 ph-Toranrhir Pronertv Dispersing Aqent Process A roces B Samole Coupler Dmin Dmax Dmin Dmax Comparison R- 0.08 2.10 0.08 1.97 A-i 0.09 2.17 0.08 2.14 A-9 0.08 2.20 0.08 2.16 (Note i1) Y-i A-11 0.09 2.21 0.08 2.19 A-20 0.08 2.19 0.08 2.15 A-26 0.08 2.19 0.08 2.15 Comparison R-1 0.09 2.66 0.09 2.48 A-i 0.09 2.70 0.09 2.64 A-9 0.09 2.71 0.08 2.67 (Note I) M-1 A-11 0.10 2.67 0.09 2.62 A-20 0.10 2.68 0.09 2.65 A-26 0.10 2.67 0.09 2.66 Comparison R-1 0.11 2.77 0.10 2.58 A- 0.10 2.79 0.09 2.71 A-9 0.10 2.78 0.09 2.70 (Note 1) C-1 A-11 0.11 2.77 0.09 2.69 A-20 0.11 2.78 0.09 2.77 A-26 0.10 2.78 0.09 2.71 (Note 1): Samples and processed by Process B are samples in this invention.

51 From the results in Table 1, it can be seen that in any cases of using yellow coupler, magenta coupler, and cyan coupler, respectively, the samples in this invention show higher maximm i density than those of comparison samples and show almost the same coloring property as in Process A, even in Process B not using benzyl alcohol.

EXAMPLE 2.

Comparison multilayer color photographic paper (A) having the layer construction shown in Table 2 below on a paper support both surface of which had been laminated by polyethylene was prepared.

In addition, the coating solutions for the layers were prepared as follows.

Preparation of coating solution for Layer 1 To 19.1 g of yellow coupler and 4.4 g of color image stabilizer were added 27.2 ml of ethyl acetate and 7.9 ml of solvent to dissolve the aforesaid components, the solution was added to 185 ml of an aqueous 10% gelatin solution containing 12 ml of a 10% solution of sodium dibutylnaphthalenesulfonate (R i) as a dispersing agent, and the mixture was emulsified by a continuous stirrer to provide an emulsified dispersion.

On the other hand, a blue-sensitive sensitizing dye shown below was added to a silver ohlorobromide emulsion (containing 80 mol% silver bromide and 70 g/kg of silver) in 52 -4 an amount of 7.0 x 10 mol per mol of silver chlorobromide to provide 90 g of a blue-sensitive emulsion.

The emulsified dispersion was mixed with the emulsion and the concentration of gelatin was adjusted as shown in Table 2 to provide the coating solution for Layer 1.

The coating solutions for Layer 2 to Layer 7 were also prepared by the same manner as for the coating solution for Layer 1.

In addition, as a gelatin hardening agent for each layer, l-oxy-3,5-dichloro-s-triazine sodium salt was used.

Also, for each emulsion layer, the following spectral sensitizer was used.

Blue-Sensitive Emulsion Layer:

S

l -OH= (CH2)4 SO 3 (OH2) SO3Nn x 10 4 mol per tiol of silver halide) r,

I

53 Green-Sensitive Pniulsion Layer: .uh=u- CH (COH 2 3 so ED- (CH2) 2

SOHN(C.H

5 x 10-4 rol pe~r mo). of silver halide) and

CI

S0 3 H-N (0 2 H95 3 x 10- 5 ol per mo). of silver halide) 54 Red-Sensitive Emule.on Layer:

OH

3

OH

3

S

O

2

H

5 10 2

H

x 10- 4 mol per niol of silver halide) Also, for each emiulsion layer was used the following dye as an irradiation preventing dye: Green-Sensitive Emlolsion Layer: HOOC- -OH-CH-=OH OOOH

NN

N1 HO N r0.

S0 3 K S0 3

K

Red-sensitive Emulsion Layer:

H

5 0 2.000 H-GH=CH- CH==CH7-WCOH HO N S0 3

K

The structural formulae of thp compounds such as couplers, etc., used in-.the example were as follows.

Yellow Coupler (a)

OH

3

OH

3 -C -COCHOONH-

II

OHN

H, I M

I

F

56 Color Image Stabilizer (b) (t)C 4

H

9 HO-~ CH 2 (t)0 4

H

9 0

OH

3 Solvent (c) 000 4

H

9 G0C0H 9 Color Stain Preventing Agent (d)

G

8 H 17 (SeC) (ec)C 8 H 17

OH

2 k1 we I till Magenta Coupler (e) IN

'NH

aCH' 2 NHSO 2 CH 3 00 H 1 8 17 O~8-n17 NHSO 2

O

8

H

1 7 (t Color Image Stabilizer (f)

OH

3

OH

3 0 3

H

7 0 -73H 00 3

H

7

COH

3 H 3 0 3

H

solvent (g) r:= C8H1 0)

P-

and 0 3 o P=O 3 2:1 mixture (weight ratio) Tr ONr 58 Ultraviolet Ray Absorbent (h) CA0 C 4

H

9 (t)

CAH

9 (t) CA OH 4 H 9 OH9 ,0H 9 (c and 0H 2

CH

2 0000 8 H 17 1:5:-3 Mixture (mol raltio) Color Stain Preventing Agent (i)

H

SC

8

H

17 (t) (t)0 8 H 1 7

OH

Solvent (j)

IOCH

1 9 O)-T.p 0 59 Cyan coupler Wk

G

5 H I I(L)

OH

C~e NHCOCHO- 5 I N I -3 0 2

HS

C 2- G.9 ul-tra±violet Ray Absorbent (1) and 11 CAN

(SC)

Nt 1;"1:3 Mixture (nio3 ratio) solvent (mn) (Me~O-

'C-

7 Z1, Layer Layer 7 (Protective layer) Layer 6 (Ultraviolet Ray Absorptive Layer) Layer 5 (Red- Sensitive Layer) Layer 4 (Ultraviolet Ray Absorptive Layer) Layer 3 (Green- Sensitive Layer) Layer 2 (Color Stain Preventing Layer) Table 2 Main Components Gelatin Acryl-modified copolymer (modified degree of 17%) of polyvinyl alcohol Gelatin Ultraviolet Ray Absorbent (h) Solvent (j) Silver chlorobromide emulsion (silver bromide 70 mol%) Gelatin Cyan Coupler (k) Color Image Stabilizer (A) Solvent (m) Gelatin Ultraviolet Ray Absorbent (h) Color Stain Preventing Agent (i) Solvent (j) Silver chlorobromide emulsion (silver bromide 75 mol%) Gelatin Magenta Coupler (e) Color Image Stabilizer (f) Solvent (g) Gelatin Color Stain Preventing Agent (d) Amount 1.33 g/m 2 0.17 0.54 0.21 0.09 cc/m 2 0.23 g/m 2 as silver 0.98 g/m 2 0.30 0.17 0.23 cc/m 2 1.60 g/m 2 0.62 0.05 0.26 cc/m 2 0.13 g/m 2 as silver 1.80 g/m 2 0.30 0.20 0.68 cc/m 2 0.99 g/m 2 0.08 Table 2 (cont Layer Layer 1 (Bluesensitive layer) Support t.) Main Components Amount Silver chlorobromide emulsion 0.27 g/m 2 (silver bromide 80 mol%) as silver Gelatin 1.86 g/m 2 Yellow Coupler 0.71 Color Image Stabilizer 0.19 Solvent 0.34 cc/m Polyethylene-laminated paper (containing white pigment (Tio 2 and bluish dye (ultramarine blue) in polyethylene at Layer 1 side) 2 Then, light-sensitive materials to were prepared as follows.

Light-Sensitive Material B Same light-sensitive material as Light-Sensitive Material except that 1.2 g of Compound A 1 of this invention.was used in place of R 1 in Layers 1, 3 and 5 of Light-Sensitive Material as a dispersing agent.

Light-Sensitive Material C Same light-sensitive material as Light-Sensitive Material 'except that 1.2 g of Compound A 9 of this invention was used in place of R 1 in Layers 1, 3 and 5 of Light-Sensitive Material as a dispersing agent.

Light-Sensitive Material D Same light-sensitive material as Light-Sensitive Material except that 1.2 g of Compound A 26 of this invention was used in place of R 1 in Layers 1, 3 and 5 of Light-Sensitive Material as a dispersing agent.

These samples were subjected to gradation exposure for sensitometry through each of blue, green, and red filters using a sensitometer (Type FWH, made by Fuji Photo Film Co, Ltd., color temperature of light source: 3,200"K).

In this case, the exposure was performed such that the exposure amount became 250 CMS in an exposure time of second.

Thereafter, the samples were processed by Process A or Process B using Color developer or respectively.

The process was composed of the steps of color development, blix, and wash and by changing the developing time to 1 minute, 2 minutes, and 3 minutes, the evaluation of the photographic properties were performed. Process A differs from Process B in the content between Color Developers A ahd B and other contents are same in both processes.

The evaluation of the photographic properties was performed on the four items of relative sensitivity, gradation, maximum density (Dmax), and minimum density (Dmin).

y The relative sensitivity was a relative Value taking the

I,

sensitivity of each light-sensitive layer of each lightsensitive material color developed for 2 minutes in Process A as 100. The sensitivity was represented as a relative value of a reciprocal of an exposure, amount necessary for (ji

L

giving a density of the minimum density 0.5. The gradation was represented as the difference in density between th~e sensitive point to a point increased by 0.5 in logarithm (logE) of exposure amount.

The results obtained are shown in Table 3 and (Processing Step) (Temperature) Development 38 0

C

Bl ix 33 0

C

Wash 28 to 35 0

C

(Color Developer Composition) color Developer Diethylenetriaminepentaacetic acid Salt Benzyl Alcohol Diethylene Glycol Na2 s03 KBr Hydroxy3.amine Sulfate 4-Amino-3-rnethyl-N-ethyl-N-[a- (rethanesulfonamido) ethylj-pphenylenediamine .Sulfate Na 2 CO 3 (monohydrate) rightonig Agent (stilboneseries) Water to ma]~e (PHl I (Time) 1.0 to 3.0 min.

1.5 min.

3.0 min.

2.0Q g 15 ml 10 ml 2.0 g 0.5 g 3.0 g 30.0 1.0 9 ,000 ml color Developer Diethylenetriaminepentaacetic acid Salt Na 2so3 KBr Hydroxylamine Sulfate 4 -Amnino- 3-me thyl ethyl-N-C- (methanesul f onamido) ethyl] -ppheny'lenediamine Sulf ate Na 2

CO

3 (mc,5nohydrate) Brightening Agent (stilbeneseries) Water to make (Blix Solution Composition) Amnmonium Thiosulfate (54 wt.%) Na 2so3 NH 4 Fe(III) (EDTA)J EbTAf2Na Water to make 30.0 1.0 g 100ml PH 10.1) 150 ml 15 g 55 g 4 g 1,000 ml (PH 6.-9) L_

K'

C Table 3A Process A -Developing Time Light-Sensitive Material Dispersing Layer Agent I minute 2 minutes RS Gd Dmin Dmax R-S Gd Dmin Dmax RS 3 minutes Ga Dmin Dmax R-1 A-1 A- 9 A-26 53 0.89 65 1.14 68 1.24 57 0.97 71 1.25 74 1.37 0-93 68 1.20 71 1,30 1.00 76 1.27 77 1.38 0.10 0.10 0.10 0.09 0.10 0.10 0.10 0.10 0.10 0.10 0.10 0.10 1.78 2.34 2.50 1.81 2.35 2.51 1.81 2.37 2.53 2.02 2.3; 2.55 100 0.92 100 1.16 100 1.26 100 1.01 100 1.28 100 1.39 100 0.97 100 1.22 100 1.32 100 1.02 100 1.28 100 1.40 0.10 0.11 0.11 0.10 0.10 0.10 0.10 0.09 0.10 0.10 0.10 0.10 1.84 2.40 2.53 1.87 2.44 2.55 1.87 2.43 2.56 1.89 2.45 2.58 106 1.00 111 1.19 114 1.28 116 130 125 ill 117 119 117 122 125 1.10 1.31 1.41 1.05 1.25 1.34 1. 12 1.33 1.43 0.11.

0.11 0.10 0.11 0.11 0.11 0.10 0.11 0.10 0.10 0.10 0 .10 2=54 1.89 2.46 2.57 1.89 2.46 2.57 1.92 2.49 2.59 RS- Relative Sensitivity Gd: Gradation h- Taole 3B Process B Developing Time Light-Sensitive Dispersing 1 minute 2 minutes 3 minutes Material Layer Agent RS Gd Dmin Dmax RS Gd Dmin Dmax RS Gd Dmin Dmax B 46 0.78 0.10 1.57 72 0.80 0.10 1.60 87 0.90 0.10 1.70 A G R-1 61 1.00 0.10 2.05 72 1.10 0.10 2.07 92 1.12 0.10 2.11 R 59 1.10 0.10 2.21 75 1.15 0.10 2.20 94 1.20 0.10 2.30 B 49 0.85 0.08 1.74 107 1.06 0.09 1.79 85 1.08 0.09 1.86 B G A-1 66 1.10 0.08 2.28 120 1.26 0.10 2.39 90 1.28 0.09 2.43 R 64 1.21 0.08 2.46 115 1.35 0.09 2.49 92 1.39 0.09 2.54 B 48 0.90 0.09 1.73 103 1.03 0.09 1.84 105 1.05 0.10 1.87 C G A-9 64 1.05 0.09 2.23 109 1.20 0.09 2.43 111 1.22 0.10 2.45 R 62 1.16 0.09 2.32 111 1.27 0.09 2.53 113 1.31 0.10 2.55 B 52 0.88 0.09 1.75 110 1.08 0.10 1.86 113 1.10 0.10 1.88 D G A-26 69 1.12 0.09 2.25 116 1.30 0.10 2.45 118 1.32 0.10 2.47 R 67 1.23 0.09 2.78 117 1.39 0.10 2.53 120 1.41 0.10 2.57 RS: Relative Sensitivity Gd: Gradation (Note Light-Sensitive Materials and processed by Process B are samples in this invention.

67 As shown in Table 3, it can be seen that Light- Sensitive Materials to for use in this invention give less difference in relative sensitivity, gradation, and maximum density between the case of processing by Process A and the case of processing by Process B as compared with Comparison Light-Sensitive Material and show almost the same performance as the case of processing in Process A, even in Process B containing no benzyl alcohol.

Also, Light-Sensitive Materials to for use in this invention show good photographic properties by the development of 2 minutes in Process B containing no benzyl alcohol even in the case of using the high-bromine containing emulsion showing relatively slow development. Therefore, it can be seen that the development time is more shortened in the case of using a high-chlorine containing emulsion.

[INDUSTRIAL APPLICABILITY] By the practice of this invention, the pollution load and work for preparing color developer can be reduced by substantially omitting benzyl alcohol and further in such a case, the effect for preventing the reduction in density by a cyan dye remaining as a leuco compound can be obtained.

Also, by using the silver halide emulsions for use in this invention, such effect that photographic properties of high Dmax, low Dmin, and less change of sensitivity and gradation

L

are obtained even in the case of using no benzyl alcohol is provided.

Claims (20)

1. A color image-forming process, which comprises processing, after imagewise exposure, a silver halide color photographic light-sensitive material comprising a reflec- tive support having provided thereon at least one silver halide emulsion layer and containing an anionic surface active agent having in the molecule a fluorine-substituted ali- phatic group having 4 to 18 carbon atoms as a hydrophobic group and -SO3M or -OSO3M (wherein M represents a hydrogen atom or a cation) as a hydrophilic group in the emulsion layer or a layer adjacent thereto with a color developer containing substantially no benzyl alcohol in a time of up to 2 minutes and 30 seconds.

2. The color image-forming process as claimed in claim 1, wherein the anionic surface active agent is a surface active agent represented by following general formula (1) (Rf) -X (1) wherein Rf represents a fluorine-substituted alkyl group having 4 to 18 carbon atoms or a fluorine-substituted alkenyl group, X represents -SO 3 M or -OSO 3 M (wherein M represnets a hydrogen atom or a cation), B .represents a di- valent or tri-valont organic residue or a poly-valent group formed by bonding of a di-valent or tri-valent organic residue and a di-valent linkage group; n represents 1 or 2; and m represents 0 or 1.

3. The color image-forming process as claimed in claim 2, wherein the di-valent or tri-valent organic residue represented by B is a di-valent or tri-valent aliphatic hydrocarbon group, an arylene group, or a di-valent hetero- cyclic group.

4. The color image-forming process as claimed in claim 2, wherein the poly-valent group represented by B is R 1 (SO -N-R -O-CO)2 R2- -COOR 1 -RIO-CO-R -CONH-R-, or -SO NR-R (wherein R represents a hydrogen atom or an alkyl 2 1 b group having 1 to 18 carbon atoms, R represents a di-valent aliphatic hydrocarbon group, an arylene group, or a di- valent heterocyclic group, and R 2 represents a tri-valent aliphatic hydrocarbon group). The color image-forming process as claimed in claim 1, wherein the silver halide emulsion layer or the layer adjacent thereto contains a fluorine-unsubstituted inionic surface active agent and/or a nonionic surface active agent together with the anionic surface active agent.

6. The color image-forming process as claimed in claim wherein the fluorine-unsubstituted anionic surface active agent is a fluorine-unsubstituted anionic surface active agent having a hydrophobic group ha .,ng 8 to 30 carbon atoms -<i 71 and an -SO3M or -OSO3M group in the molecule.

7. The color image-forming process as claimed in claim wherein the nonionic surface active agent is a sorbitan fatty acid ester-series nonionic surface active agent.

8. The color image-forming process as claimed in claim 1, wherein the color developer is an alkaline aqueous solution containing an aromatic primary amine-series color developing agent as the main component.

9. A color image-forming process which comprises sub- jecting, after imagewise exposure, a silver halide color photographic light-sensitive material comprising a reflec- tive support having provided thereon at least one red- sensitive silver halide emulsion layer, at least one green- sensitive silver halide emulsion layer, and at least one blue-sensitive silver halide emulsion layer to color devel- opment, bleach and or blix, and wash and/or stabiliza- tion, said silver halide emulsion layer or a layer adjacent thereto containing an anionic surface active agent having in the molecule a fluorine-substituted aliphatic group having 4 to 18 carbon atoms as a hydrophobic group and -SO 3M or -OSO 3 M (wherein M represents a hydrogen atom or a cation) as a hydrophilic group and said color development being per- formed with a color developer containing substantially no benzyl alcohol in a time of up to 2 minutes and 30 seconds. The color image-forming process as claimed in claim i 9, wherein the anionic surface active agent is a surface active agent represented by following general formula (1) (Rf) (1) wherein Rf represents a fluorine-substituted alkyl group having 4 to 18 carbon atoms or a fluorine-substituted alkenyl group, X represents -SO 3 M or -OSO 3 M (wherein M represnets a hydrogen atom or a cation), B represents a di- valent or tri-valent organic residue or a poly-valent group formed by bonding of a di-valent or tri-valent organic residue and a di-valent linkage group, n represents 1 or 2, and m represents 0 or 1.

11. The color image-forming process as claimed in claim wherein the di-valent or tri-valent organic residue represented by B is a di-valent or tri-valent aliphatic hydrocarbon group, an arylene group, or a di-valent hetero- cyclic group.

12. The color image-forming process as claimed in claim wherein the poly-valent group representea by B is *R (S02-N-R 1 -0-CO) 2 R 2 -COOR-,' -RO0-CO-R 1 -CONH-RI-, or -S02NR-R 1 (wherein R represents a hydrogen atom or an alkyl group having 1 to 18 carbon atoms, R i represents a di-valent aliphatic hydrocarbon group, an arylene group, or a di- 73 valent heterocyclic group, and R represents a tri-valent aliphatic hydrocarbon group).

13. The color image-forming process as claimed in claim 9, wherein the silver halide emulsion layer or the layer adjacent thereto contains a fluorine-unsubstituted anionic surface active agent and/or a nonionic surface active agent together with the anionic surface active agent.

14. The color.image-forming process as claimed in claim 13, wherein the fluorine-unsubstituted anionic surface ac- tive agent is a fluorine-unsubstituted anionic surface ac- tive agent having a hydrophobic group having 8 to 30 carbon atoms and an -SO M or -OSO 3 M group in the molecule. The color image-forming process as claimed in claim 13, wherein the nonionic surface active agent is a sorbitan fatty acid ester-series nonionic surface active agent.

16. The color image-forming process as claimed in claim 9, wherein the color developer is an alkaline aqueous solu- tion containing an aromatic primary amine-series color developing agent as the main component.

17. The color image-forming process as claimed in claim S1, wherein the silver halide is of a type mainly forming latent images on the surface of the grain.

18. The color image-forming process as claimed in claim 1, wherein the color developer contains no benzyl alcohol.

19. The color image-forming process as claimed in claim L_ 74 8, wherein the aromatic primary amine-series color devel- oping agent is a p-phenylenediamine-series compound. The color image-forming process as claimed in claim 19, wherein the p-phenylenediamine-series compound is 3- methyl-4-amino-N-ethyl-N-3 -methanesul fonamidoethyl aniline or 3-methyl-4-amino-N-ethyl-N-hydroxyethylaniline.

21. The color image-forming process as claimed in claim 19, wherein the p-phenylenediamine-series compound is 3- methyl-4-amino-N-ethyl-N- -methanesul fonamidoethylaniline.

22. The color image-forming process as claimed in claim 1, wherein the anionic surface active agent is contained in the silver halide emulsion layer.

23. The color image-forming process as claimed in claim 1, wherein the anionic surface active agent is contained in the silver halide emulsion layer and/or a layer adjacent thereto i n an mount of 0.2 to 50% by weight to a hydro- phobic substance dispersed by emulsification in said layer. TJ- ABSTRACT OF THE DISCLOSURE A color image forming process which comprises pro- cessing, after imagewise exposure, a color photographic paper containing an anionic surface active agent having a fluorine-substituted aliphatic group as a hydrophobic group and -SO3M or -OSO3M (wherein M is a hydrogen atom or a cation) as a hydrophilic group. In the case of processing the color photographic paper containing the aforesaid fluorine-substituted anionic surface active agent, color images having high color density are obtained in a short period of time even by processing it with a color developer containing substantially no develop- ment accelerator causing pollution. U INTERNATIONAL SEARCH RiEPORT International Application No, PCT/ JP87 /000 62 1. CLASSIFICA TION OF SUBJECT MATTER il several ciassification symbols apply, Indicate all) According to international Patent Classification ltPCi or to t2nth National Classitication and IPC Int.C1 4 G0327/30, GO3C7/26 11. FIELDS SEARCHED Minimum Documentation Searched4 Ciassiticaton System Classification Symbols IPC I G03C7/30, G03C7/26 Documentation Searched other than Minimum Documentation to the Extent that such Documents are Included In the Filds Searched

111. DOCUMENTS CONSIDOIED TO HE RELEVANT" Category' Citatio'n of Document, Owith lhdication, where aporuoPriate, ot the reievant passages'eian to Ciaim No. 8 1 A JP, A, 60-158446 (Konishiroku Photo 1. I.nd, Co., Ltd.) 19 AuUSt 1985 (19. 08. (Family: none) A, JP, A, 51-129229 (Fuji Photo Film Co., Ltd.) November 1976 (10. 11, 76) DZ, Al, 2619248 GB, A, 1507961 USt A, 4385110 A JP, A, 59-72442 (Konishiro}ku Photo1 Inmd. Co.i Ltd.) 24 April 1984 (24. 04. 84) (Family: none) *Special Categories of cited documnenits: later document Published after the InternationO~ flinrg date or ilorzui'ent detining the general state ot the art which is not priority date and not In contttct with the apcicatloi but cited to qonsileisd to be ot partilulae reievatnce understand the principle or theory undzerlying the krivntlon "E"ealerdoumet utpublished on or altar the international, document of particular retevance, the claimed inhientlon cannol fi, alier docenbu be considered novel or cannot be considerod to invoiye an IL" document which may throw doubts on priority clalm~st or ivniese which Is cited to entabiab the publicatior Ite ot another "iY" document o( parlilaf relevance: o:e 1i1almed Invention cannot citation or Other speciat reason las specitlg. be considered to Involve an inventive step when the document is combined with one or more other such documents, such documeril reterring to an oral disclosure, use, exhibition or combination being obvious, to a p~rsgn skilled in the art othor meas"6 document member a1 the same pai~irir famiiti '111 document published prior to the intei,sl.tlonal tiling date but later than tWe priority date claimed WV. CERTIFICATION Date W~ the Actual Conipletipo of the International Search zDate of Mailing of ihitf, International Search Report April 27, 1987 (27. Q4. 87) 1 M4ay 6, 1987 05. 071% International Searching Authority' Signature of Authorized Otficer Japanese Patent OfficeI Farted rCT/ISAi2tO (second aheell, 104tober' 119111 UIPC) In t. C-V G03C7/30, GO3C,T/26 I PC G03C7/30, G03C7/26 A JP, A. 60-1 5 8 4 46 T 1 9. 8,9. 1 98 5( 19. 0 8. 8 A JP ,51-1 1 1 0. 1 1 A. 197 6 10. 1 1. 76) &DE, Al. 26 19248&GB, A. 1507961 &US, A. 4385 11 0 A JP, A, 59-7 2 44 2(4N AN -1FX1 2 4. 4A. 19 8 4(24. 0 4. 8 4) -t U) I ~U FE" fWNl61 zbi P6( "I j 2A?. 04.f 87 X06.05.37 A z &A D 4 2 7i 9 Q I z. Att141MtBXk59,iitft~:L9L6t; t E't/IA/t 2 V) (1A398i6 6 c e-C15O 10 'A(