JPH04204648A - Method for processing silver halide color photographic sensitive material - Google Patents

Method for processing silver halide color photographic sensitive material

Info

Publication number
JPH04204648A
JPH04204648A JP33450590A JP33450590A JPH04204648A JP H04204648 A JPH04204648 A JP H04204648A JP 33450590 A JP33450590 A JP 33450590A JP 33450590 A JP33450590 A JP 33450590A JP H04204648 A JPH04204648 A JP H04204648A
Authority
JP
Japan
Prior art keywords
processing
water
washing
silver halide
fixing
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP33450590A
Other languages
Japanese (ja)
Inventor
Makoto Nishimura
誠 西村
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
CHIYUUGAI SHASHIN YAKUHIN KK
Chugai Pharmaceutical Co Ltd
Original Assignee
CHIYUUGAI SHASHIN YAKUHIN KK
Chugai Pharmaceutical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by CHIYUUGAI SHASHIN YAKUHIN KK, Chugai Pharmaceutical Co Ltd filed Critical CHIYUUGAI SHASHIN YAKUHIN KK
Priority to JP33450590A priority Critical patent/JPH04204648A/en
Publication of JPH04204648A publication Critical patent/JPH04204648A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To enhance stability of photographic image quality without using a large amount of rinsing water by processing the imagewise exposed photo graphic sensitive material with a fixing solution and a bleach-fixing solution and then processing it with a processing solution containing 2-aminobenzo thiazole in place of rinsing with water. CONSTITUTION:The exposed photographic sensitive material is processed with the fixing solution comprising thiosulfate, a processing solution to be used following the fixing instead of rinsing, and the bleach-fixing solution comprising the ferric salt of aminopolycarboxylic acid and thiosulfate, and the processing solution containing the 2-aminobenzothiazole, to be used in place of rinsing, thus permitting processing superior in stability in the case of using for a long time to be executed and the photographic image obtained by this processing to be enhanced in stability.

Description

【発明の詳細な説明】[Detailed description of the invention]

(イ)産業上の利用分野 本発明はハロゲン化銀カラー感光材料の処理方法に関し
、更に詳しくは、定着処理後の水洗処理に代り処理液を
使用する処理方法、及び漂白定着処理後の水洗処理に代
り処理液を使用する処理方法に関するものである。 (ロ)従来の技術 ハロゲン化銀カラー感光材料の処理は、発色現像処理の
後、アミノポリカルボン酸の鉄塩とハロゲン塩を含有す
る漂白液で処理し、次てチオ硫酸塩を含有する定着液で
処理し、流水により水洗処理を行い、又、発色現像処理
の後、アミノポリカルボン酸の鉄塩とチオ硫酸塩を含有
する漂白定着液で処理し、流水により水洗処理を行って
おり、この様にしてハロゲン化銀カラー感光材料を処理
する場合安定的に多量に処理する方法として、処理する
感光材料の量に応じて必要な量の処理液を補充液として
補充する方法で行われている。 近年この補充量は少量となり、使用後排出される処理液
の量も少量であるため容器に回収する事が可能となって
いる。 一方水洗処理は多量の水を使用して行っており、多量の
水洗水を使用する事から使用後の排水を容器に回収する
事は不可能であり、ハロゲン化銀カラー感光材料を処理
する自動現像機には、この水洗のため給水と使用後の排
水のための施設が必要となり、この施設のために自動現
像機の設置場所が制限される事となる。更に多量に使用
する水洗水は水洗に適した水温で使用するため適温水を
得るため多くの燃料が必要であり、コスト上昇の一因と
なっている。 このため種々の方法が試みられており、その一つとして
少量の水洗水で効率良く水洗を行うため、多くの水洗槽
を独立して使用して感光材料の流れと逆に水洗水を流す
カスケード方法は古くから知られている。この方法は効
率良く水洗が出来るのは確かで、手現像処理の様に少量
の写真を処理するのであればその目的をを十分にはたす
。今日の様に自動現像機を使用して多量に連続的に感光
材料を処理する場合でも自動現像機の水洗方法として利
用出来、多数の水洗槽を持つ様になっている。この水洗
槽は水洗の最後の槽から水洗水を加え、溢れる分を順次
前の槽に送り、この流れとは逆に感光材料が送られ感光
材料は順次新しい水で水洗されながらこの工程を終る事
になる。 このような自動現像機を使用する場合、水洗の前の工程
である定着液又は漂白定着液が処理される感光材料によ
り運ばれて各水洗槽で一定の温度となるが、本来は分解
はしない定着液又は漂白定着液でも、多くの水洗槽の内
のあるものでは組成のバランスがくずれ分解が生じ、こ
れにより画質を低下させる原因となり合せて、出来得る
限り少量の水洗水で効率良い水洗を行うためにはカスケ
ードで結ばれた水洗槽を多くすれば良いが、こうする事
で水洗水が使用され排出水となるまで水洗槽に滞留する
時間が長くなり微生物の発生があり、画像に付着する欠
点が発生すると同時に、水洗の効率を上げるため水洗槽
を多くする事は、自動現像機施設のスペースを大きくす
る欠点が表面化して来る。 (旧 解決すべき点 このような欠点を無くするための新しい方法が要望され
ており、その方法として2〜3槽の水洗槽をカスケード
で結び、少量の補充による処理液で処理する事でその目
的の一つを達成しており、更に良質の画像とこの画像の
安定性が十分な画像を得る事が出来る様に処理液を使用
し1合せて少ない処理槽の自動現像機でスペースの減少
と、少量の処理液を使用する事で排出される液量の減少
から容器による回収を可能とし、水洗に対する給排水設
置が必要で無くなり、施設場所の制限が無くなる。 こうした少数の水洗槽で処理するに当り、良質の画像を
得、更にこの画像の安定性が十分良く、処理水の安定性
、処理効率の向上が必要である。自動現像機を使用して
効率良く多量にハロゲン化銀感光材料を安定的に処理を
継続するためには使用する処理液は安定でなくてはなら
ず、安定性の高い処理方法が望まれている。 (:)  問題点を解決するための手段本発明は、チオ
硫酸塩を含有する定着液に続く水洗処理に代り、処理液
を使用する方法及びアミノポリカルボン酸の鉄塩とチオ
硫酸塩を含有する漂白定着液に続く水洗処理に代り処理
液を使用する方法に関するものであり、その目的は長期
間使用するに当り安定性の優れた処理が出来、更に処理
された写真画像の安定性を向上させる事の出来るように
したもので、チオ硫酸塩から成る定着液に続く水洗処理
に代り使用する処理液及びアミノポリカルボン酸の鉄塩
とチオ硫酸塩がら成る漂白定着液に続(水洗処理に代り
使用する処理液に、2−アミノベンゾチアゾールを含む
処理液を使用する事を特徴とする。 (幻実施例 以下に実施例により本発明の詳細な説明するが、これに
より本発明の実施態様が限定されるものではない6
(a) Industrial Application Field The present invention relates to a method for processing silver halide color light-sensitive materials, and more specifically, a processing method using a processing solution instead of washing with water after fixing, and washing with water after bleach-fixing. The present invention relates to a processing method that uses a processing liquid instead of. (b) Conventional technology Silver halide color light-sensitive materials are processed using a bleaching solution containing an iron salt of aminopolycarboxylic acid and a halogen salt after color development, followed by fixing containing a thiosulfate. After processing with a bleach-fixing solution containing an iron salt and thiosulfate of aminopolycarboxylic acid and washing with running water, When processing silver halide color light-sensitive materials in this manner, a method for stably processing a large amount of light-sensitive materials is to replenish the necessary amount of processing solution as a replenisher depending on the amount of light-sensitive material to be processed. There is. In recent years, the amount of replenishment has become small, and the amount of processing liquid discharged after use is also small, so it has become possible to collect it in a container. On the other hand, the washing process uses a large amount of water, and because it uses a large amount of washing water, it is impossible to collect the waste water after use into a container. The developing machine requires facilities for water supply and drainage after use for washing, and this facility limits the installation location of the automatic developing machine. Furthermore, since the large amount of washing water used is used at a water temperature suitable for washing, a large amount of fuel is required to obtain the water at the appropriate temperature, which is one of the causes of increased costs. Various methods have been tried for this purpose, one of which is a cascade system in which many washing tanks are used independently and the washing water flows in the opposite direction to the flow of the photosensitive material, in order to perform washing efficiently with a small amount of washing water. The method has been known for a long time. It is true that this method allows for efficient washing with water, and it satisfies the purpose of processing small quantities of photographs, such as hand-processing. Even when automatic processors are used today to continuously process large amounts of photosensitive materials, automatic processors can be used as a washing method, and many washing tanks are now provided. In this washing tank, washing water is added from the last washing tank, and the overflow is sent to the previous tank in order.The photosensitive material is sent in the opposite direction to this flow, and the photosensitive material is sequentially washed with new water to complete the process. It's going to happen. When using such an automatic processor, the fixing solution or bleach-fixing solution, which is the step before washing, is carried by the photosensitive material being processed and reaches a constant temperature in each washing tank, but it does not decompose. Even with the fixing solution or bleach-fixing solution, in many washing tanks, the composition of some liquids becomes unbalanced and decomposition occurs, which causes deterioration of image quality. In order to do this, you can increase the number of washing tanks connected in a cascade, but this will increase the amount of time the washing water remains in the washing tank until it is used and becomes waste water, which may cause the generation of microorganisms that may adhere to the image. At the same time, increasing the number of washing tanks in order to increase the efficiency of water washing has the disadvantage of increasing the space of the automatic processor facility. (Old Points to be Solved) A new method is required to eliminate these drawbacks, and this method involves cascading two or three washing tanks and treating them with a small amount of replenishing processing solution. One of the objectives has been achieved, and furthermore, in order to obtain images with sufficient quality and image stability, we use a processing solution and reduce space by using an automatic developing machine with a total of fewer processing tanks. By using a small amount of processing liquid, the amount of liquid discharged is reduced, making it possible to collect it in a container, eliminating the need for water supply and drainage installation for washing, and eliminating restrictions on facility location. Processing with such a small number of washing tanks In order to obtain high-quality images, it is necessary to have sufficient stability of these images, and to improve the stability of treated water and processing efficiency.Silver halide photosensitive materials can be efficiently produced in large quantities using automatic processors. In order to stably continue processing, the processing liquid used must be stable, and a highly stable processing method is desired. , a method in which a processing solution is used instead of a washing treatment followed by a fixing solution containing a thiosulfate, and a method in which a processing solution is used instead of a washing treatment followed by a bleach-fixing solution containing an iron salt of an aminopolycarboxylic acid and a thiosulfate. The purpose of this technology is to provide processing with excellent stability over long-term use, and to improve the stability of processed photographic images. A processing solution used instead of washing with water followed by a fixing solution containing 2-aminobenzothiazole, followed by a bleach-fixing solution containing iron salt and thiosulfate of aminopolycarboxylic acid (the processing solution used instead of washing with water contains 2-aminobenzothiazole) The present invention is characterized by using a processing liquid.

【実施例 1】 小型自動現像機を使用して、市販カラーフィルムを次の
様に処理した。 処理工程 発色現像液 無水亜硫酸ナトリウム    3.5g無水炭酸カリウ
ム     35.ogg化カリウム        
 1.2g硫酸ヒドロキシルアミン   2.5gジエ
チレントリアミン五酢酸 1.0g水酸化ナトリウム 
     l、0g水を加えて         1.
 Off発色現像補充液 無水亜硫酸ナトリウム    4.0g無水炭酸カリウ
ム     40.0g臭化カリウム        
1,0g硫酸ヒドロキシルアミン   3.Ogジエチ
レントリアミン五酢酸 1.5g水酸化ナトリウム  
    l、0g水を加えて         1.O
R漂白液 臭化アンモニウム    140.0gエチレンジアミ
ン四四節鉄アンモメウム    90.  ogエチレ
ンジアミン四酢酸   5.0g水を加えて     
    1. OI2漂白補充液 臭化アンモニウム    170.0gエチレンジ7ミ
ン四酢酸鉄アンモヌウム  110.ogエチレンジア
ミン四酢酸   8.0g水水酸酸         
 5 、 Q g水を加えて         1.0
β定着液 チオ硫酸アンモニウム  140.0g重亜硫酸ナトリ
ウム    14.0gアンモニア水        
5.0g水を加えて         1. OI2定
着補充液 チオ硫酸アンモニウム  170.0g重亜硫酸ナトリ
ウム    17.0gアンモニア水       1
0.0g水を加えて         1.0&安定液 ホルマリン         5.0+n水を加えて 
        i、o!l安定補充液 上記安定液を使用する。 処理するに当り発色現像の補充量は35m+wフィルム
1本当り38+n。漂白、定着、安定の補充量は35r
RII+、フィルム1本当り31nで行った。 定着処理に続く処理は次の様に行った。 (l135++c+++フィルム1本当り620mの水
洗(これまでの方法) f2)35+n+nフィルム1本当り31mの水洗6(
水比較方法) (3)35mmフィルム1本当り31mの処理液を使用
、(本発明) この処理液の組成は次の通りである。 処理液 2−アミノベンゾチアゾール 0.2g水を加えて  
       1.0!前記処理方法、及び処理液を使
用して、200本処理した結果、定着処理後の処理液及
び水洗水の状態は以下の様である。 更に、一定置光を与えたカラーフィルムを処理した資料
を太陽光に照射、温度60℃、湿度70%の恒温恒湿槽
中に入れ、画像の耐久性を比較した結果は次の様である
。濃度測定に使用した濃度計は X −RI T E 
310RTである。 尚、BDは青色光濃度、GDは青色光濃度、RDは赤色
光濃度 この結果より、処理方法m、(31は水洗水及び処理液
ともその状態は良好で、更に画像汚染も無く、合せて処
理された画像劣化も無いが、処理方法 (2)は、処理
液の状態は悪く更に画像汚染、画像劣化があり、本発明
 (3)はこれまでの水洗方法に代えて使用出来ること
が分かる。
Example 1 A commercially available color film was processed as follows using a small automatic processor. Processing process Color developer Anhydrous sodium sulfite 3.5g Anhydrous potassium carbonate 35. oggated potassium
1.2g Hydroxylamine sulfate 2.5g Diethylenetriaminepentaacetic acid 1.0g Sodium hydroxide
l, add 0g water 1.
Off color developer replenisher Anhydrous sodium sulfite 4.0g Anhydrous potassium carbonate 40.0g Potassium bromide
1.0g hydroxylamine sulfate 3. Og diethylenetriaminepentaacetic acid 1.5g sodium hydroxide
l, add 0g water 1. O
R bleaching solution ammonium bromide 140.0g ethylenediamine 44-bar iron ammoumeum 90. og ethylenediaminetetraacetic acid Add 5.0g water
1. OI2 Bleach Replenisher Ammonium Bromide 170.0g Ethylenedi7minetetraacetate Iron Ammonium 110. og ethylenediaminetetraacetic acid 8.0g Hydroxylic acid
5, add Q g water 1.0
β fixer Ammonium thiosulfate 140.0g Sodium bisulfite 14.0g Aqueous ammonia
Add 5.0g water 1. OI2 Fixer Replenisher Ammonium Thiosulfate 170.0g Sodium Bisulfite 17.0g Aqueous Ammonia 1
Add 0.0g water 1.0 & stabilized formalin 5.0+n water
i,o! l Stable replenisher solution Use the above stabilizing solution. During processing, the replenishment amount of color development is 38+n per 35m+w film. The replenishment amount for bleaching, fixing, and stabilization is 35r.
RII+, 31n per film. The treatment following the fixing treatment was performed as follows. (l135++c+++ 620m of water washing per film (previous method) f2) 35+n+n 31m of water washing per 1 film 6 (
Water comparison method) (3) 31 m of processing liquid was used for one 35 mm film (invention) The composition of this processing liquid was as follows. Treatment liquid 2-aminobenzothiazole Add 0.2g water
1.0! As a result of processing 200 sheets using the above-mentioned processing method and processing liquid, the conditions of the processing liquid and washing water after the fixing process are as follows. Furthermore, materials processed from color film that were exposed to constant light were exposed to sunlight and placed in a constant temperature and humidity chamber at a temperature of 60°C and humidity of 70%, and the results of comparing the durability of the images were as follows. . The densitometer used for concentration measurement is
It is 310RT. Furthermore, BD is the blue light density, GD is the blue light density, and RD is the red light density. There is no deterioration of the processed image, but in processing method (2), the condition of the processing liquid is poor and there is also image staining and image deterioration, so it can be seen that the present invention (3) can be used in place of the conventional water washing method. .

【実施例 2】 小型自動現像機を使用して、市販カラーペーパーを次の
様に処理した。 基準処理工程 この処理に使用した各処理液の組成は次の通りである。 発色現像液 ジエチレングリコール   15.0gベンジンアルコ
ール    16.0g無水亜硫酸ナトリウム    
2.5g臭化カリウム        0.7g無水炭
酸カリウム     30.og硫酸ヒドロキシルアミ
ン   32g へキサメタン酸ナトリウム  2.0g3−メチル−4
−アミノ−N−エチル−N−1−メタンスルフォンアミ
ドエチル)アンリン硫a塩  5. 5g水酸化ナトリ
ウム      3.0g水を加えて        
 1.0ρ発色現像補充液 ジエチレングリコール   18.0gベンジンアルコ
ール    20.0g無水亜硫酸ナトリウム    
3.0g無水炭酸カリウム     30.0g硫酸ヒ
ドロキシルアミン   4.0gへキサメタン酸ナトリ
ウム  2,0g水酸化ナトリウム      4.1
g水を加えて         10! 漂漂白者液 チオ硫酸アンモニウム  100.0g無水亜硫酸ナト
リウム   15.0g炭酸ナトリウム       
5.0g水を加えて         1.Op漂白定
着補充液 チオ硫酸アンモニウム  i20.0g無水亜硫酸ナト
リウム   20.0g水を加えて         
1. OI2処理するに当り発色現像及び漂白定着の補
充量は共に1rrf当り320mで行った。漂白定着処
理に続く処理は次の様に行った。 (1)感光材料1m″当り12!の水洗(これまでの方
法) (2)感光材料1ゴ当906℃の水洗 (比較方法) (3)感光材料1rn’当り0.642の処理液を使用
(本発明) この処理液の組成は次の通りである。 処理液 2−アミノベンゾチアゾール 0.1gニトリロ三酢酸
       0,2g水酸化カリウム       
0.1g水を加えて         1.02前記処
理方法、及び処理液を使用して、150rn”処理した
結果、漂白定着処理後の処理液及び水洗水の状態は以下
の様である。 更に、一定貫光を与えたカラーペーパーを処理した資料
を太陽光に照射、温度60℃、湿度70%の恒温恒湿槽
中に入れ、画像の耐久性を比較した結果は次の様である
。濃度測定に使用した濃度計は X−RITE310R
Tである。 画像のない部分の試験前後の濃度 各々、青色光、緑色光、赤色光で露光し処理された画像
の試験前後の濃度。 尚、BDは青色光濃度、GDは青色光濃度RDは赤色光
濃度。 この結果より、処理方法+11. +31 は水洗水及
び処理液ともその状態は良好で、更に画像汚染も無く、
合せて処理された画像劣化も無いが、処理方法 (2)
は処理液の状態は悪く、更に画像汚染、画像劣化があり
、本発明の(3)はこれまでの水洗方法に代えて使用出
来ることが分かる。 (へ)発明の効果 上記の如く本発明によれば、ハロゲン化銀カラー感光材
料の処理において、定着液及び漂白定着液で処理を行っ
た後の水洗に代り、2−アミノベンゾチアゾールを含有
する処理液を使用して処理する事で、多量の水洗水を使
用する事無く、水洗水を使用しない事から給排水設置も
必要とせず、施設場所の制限が無くなりその効果は大で
ある。
Example 2 Commercially available color paper was processed as follows using a small automatic processor. Standard treatment step The composition of each treatment liquid used in this treatment is as follows. Color developer diethylene glycol 15.0g benzine alcohol 16.0g anhydrous sodium sulfite
2.5g potassium bromide 0.7g anhydrous potassium carbonate 30. og hydroxylamine sulfate 32g Sodium hexamethanate 2.0g 3-methyl-4
-amino-N-ethyl-N-1-methanesulfonamidoethyl)anline sulfate 5. Add 5g sodium hydroxide 3.0g water
1.0ρ Color developer replenisher diethylene glycol 18.0g Benzine alcohol 20.0g Anhydrous sodium sulfite
3.0g anhydrous potassium carbonate 30.0g hydroxylamine sulfate 4.0g sodium hexamethanate 2.0g sodium hydroxide 4.1
g Add water 10! Bleach solution Ammonium thiosulfate 100.0g Anhydrous sodium sulfite 15.0g Sodium carbonate
Add 5.0g water 1. Op bleach-fix replenisher Ammonium thiosulfate i20.0g Anhydrous sodium sulfite 20.0g Add water
1. During OI2 processing, the replenishment amount for both color development and bleach-fixing was 320 m/rrf. Processing subsequent to the bleach-fixing process was performed as follows. (1) Washing at a rate of 12! per meter of photosensitive material (previous method) (2) Washing at 906°C per meter of photosensitive material (comparative method) (3) Using 0.642 processing solution per rn' of photosensitive material (This invention) The composition of this treatment liquid is as follows: Treatment liquid 2-aminobenzothiazole 0.1g Nitrilotriacetic acid 0.2g Potassium hydroxide
Add 0.1 g of water 1.02 Using the above processing method and processing solution, the results of processing for 150 rn'' are as follows: The conditions of the processing solution and washing water after bleach-fixing are as follows. The results of comparing the durability of the image by exposing the processed color paper to sunlight and placing it in a constant temperature and humidity chamber at a temperature of 60℃ and humidity of 70% are as follows.Density measurement The concentration meter used was X-RITE310R.
It is T. The density before and after the test of the non-image area, respectively, and the density before and after the test of the image exposed and processed with blue light, green light, and red light. In addition, BD is blue light density, GD is blue light density, and RD is red light density. From this result, processing method +11. +31 is in good condition with both washing water and processing liquid, and there is no image stain.
There is also no image deterioration, but the processing method (2)
It can be seen that the condition of the processing liquid is poor, and there is also image staining and image deterioration, and that the method (3) of the present invention can be used in place of the conventional water washing method. (F) Effects of the Invention As described above, according to the present invention, in the processing of silver halide color light-sensitive materials, 2-aminobenzothiazole is contained instead of washing with water after processing with a fixer and a bleach-fixer. By using a treatment liquid for treatment, there is no need to use a large amount of washing water, and since no washing water is used, there is no need to install water supply and drainage, and there are no restrictions on facility location, which is highly effective.

Claims (2)

【特許請求の範囲】[Claims] (1)ハロゲン化銀カラー感光材料の処理に関し発色現
像処理後チオ硫酸塩を含有する定着液で処理を行い、続
く水洗に代り、2−アミノベンゾチアゾールを含有する
処理液を使用する事を特徴とするハロゲン化銀カラー感
光材料の処理方法
(1) Regarding the processing of silver halide color light-sensitive materials, after color development processing, processing is performed with a fixing solution containing thiosulfate, and instead of the subsequent washing with water, a processing solution containing 2-aminobenzothiazole is used. Processing method for silver halide color light-sensitive materials
(2)ハロゲン化銀カラー感光材料の処理に関し発色現
像処理後、アミノポリカルボン酸の鉄塩とチオ硫酸塩を
含有する漂白定着液で処理を行い、続く水洗に代り、2
−アミノベンゾチアゾール含有する処理液を使用する事
を特徴とするハロゲン化銀カラー感光材料の処理方法
(2) Regarding the processing of silver halide color light-sensitive materials, after color development processing, instead of processing with a bleach-fix solution containing iron salt and thiosulfate of aminopolycarboxylic acid and subsequent washing with water,
- A method for processing silver halide color light-sensitive materials characterized by using a processing solution containing aminobenzothiazole
JP33450590A 1990-11-30 1990-11-30 Method for processing silver halide color photographic sensitive material Pending JPH04204648A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP33450590A JPH04204648A (en) 1990-11-30 1990-11-30 Method for processing silver halide color photographic sensitive material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP33450590A JPH04204648A (en) 1990-11-30 1990-11-30 Method for processing silver halide color photographic sensitive material

Publications (1)

Publication Number Publication Date
JPH04204648A true JPH04204648A (en) 1992-07-27

Family

ID=18278154

Family Applications (1)

Application Number Title Priority Date Filing Date
JP33450590A Pending JPH04204648A (en) 1990-11-30 1990-11-30 Method for processing silver halide color photographic sensitive material

Country Status (1)

Country Link
JP (1) JPH04204648A (en)

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