JPS62178263A - Processing method for silver halide color photosensitive material - Google Patents
Processing method for silver halide color photosensitive materialInfo
- Publication number
- JPS62178263A JPS62178263A JP2038086A JP2038086A JPS62178263A JP S62178263 A JPS62178263 A JP S62178263A JP 2038086 A JP2038086 A JP 2038086A JP 2038086 A JP2038086 A JP 2038086A JP S62178263 A JPS62178263 A JP S62178263A
- Authority
- JP
- Japan
- Prior art keywords
- processing
- washing
- water
- silver halide
- photosensitive material
- 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
Links
- 239000000463 material Substances 0.000 title claims abstract description 21
- 229910052709 silver Inorganic materials 0.000 title claims abstract description 10
- 239000004332 silver Substances 0.000 title claims abstract description 10
- -1 silver halide Chemical class 0.000 title claims abstract description 10
- 238000003672 processing method Methods 0.000 title description 8
- 238000012545 processing Methods 0.000 claims abstract description 47
- 238000000034 method Methods 0.000 claims abstract description 26
- 239000002253 acid Substances 0.000 claims abstract description 6
- 239000000539 dimer Substances 0.000 claims abstract description 4
- 150000002505 iron Chemical class 0.000 claims abstract 2
- DHCDFWKWKRSZHF-UHFFFAOYSA-N sulfurothioic S-acid Chemical compound OS(O)(=O)=S DHCDFWKWKRSZHF-UHFFFAOYSA-N 0.000 claims abstract 2
- 238000005406 washing Methods 0.000 claims description 38
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 34
- 238000011161 development Methods 0.000 claims description 4
- 150000001447 alkali salts Chemical class 0.000 claims 1
- 239000007788 liquid Substances 0.000 abstract description 17
- 238000010186 staining Methods 0.000 abstract description 3
- 239000007844 bleaching agent Substances 0.000 abstract 3
- 230000005494 condensation Effects 0.000 abstract 2
- 238000009833 condensation Methods 0.000 abstract 2
- 159000000011 group IA salts Chemical class 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 28
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 238000011109 contamination Methods 0.000 description 5
- 229940101006 anhydrous sodium sulfite Drugs 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 4
- 230000006866 deterioration Effects 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- 239000003109 Disodium ethylene diamine tetraacetate Substances 0.000 description 2
- ZGTMUACCHSMWAC-UHFFFAOYSA-L EDTA disodium salt (anhydrous) Chemical compound [Na+].[Na+].OC(=O)CN(CC([O-])=O)CCN(CC(O)=O)CC([O-])=O ZGTMUACCHSMWAC-UHFFFAOYSA-L 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- UXGLWSHNROIPQH-UHFFFAOYSA-H [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[O-]C=O.[O-]C=O.[O-]C=O.[O-]C=O.[O-]C=O.[O-]C=O Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[O-]C=O.[O-]C=O.[O-]C=O.[O-]C=O.[O-]C=O.[O-]C=O UXGLWSHNROIPQH-UHFFFAOYSA-H 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- XYXNTHIYBIDHGM-UHFFFAOYSA-N ammonium thiosulfate Chemical compound [NH4+].[NH4+].[O-]S([O-])(=O)=S XYXNTHIYBIDHGM-UHFFFAOYSA-N 0.000 description 2
- 235000019445 benzyl alcohol Nutrition 0.000 description 2
- 235000019301 disodium ethylene diamine tetraacetate Nutrition 0.000 description 2
- 159000000014 iron salts Chemical class 0.000 description 2
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- SRFKWQSWMOPVQK-UHFFFAOYSA-K sodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxymethyl)amino]acetate;iron(2+) Chemical compound [Na+].[Fe+2].OC(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O SRFKWQSWMOPVQK-UHFFFAOYSA-K 0.000 description 2
- 150000004764 thiosulfuric acid derivatives Chemical class 0.000 description 2
- ZNBNBTIDJSKEAM-UHFFFAOYSA-N 4-[7-hydroxy-2-[5-[5-[6-hydroxy-6-(hydroxymethyl)-3,5-dimethyloxan-2-yl]-3-methyloxolan-2-yl]-5-methyloxolan-2-yl]-2,8-dimethyl-1,10-dioxaspiro[4.5]decan-9-yl]-2-methyl-3-propanoyloxypentanoic acid Chemical compound C1C(O)C(C)C(C(C)C(OC(=O)CC)C(C)C(O)=O)OC11OC(C)(C2OC(C)(CC2)C2C(CC(O2)C2C(CC(C)C(O)(CO)O2)C)C)CC1 ZNBNBTIDJSKEAM-UHFFFAOYSA-N 0.000 description 1
- GGZZISOUXJHYOY-UHFFFAOYSA-N 8-amino-4-hydroxynaphthalene-2-sulfonic acid Chemical compound C1=C(S(O)(=O)=O)C=C2C(N)=CC=CC2=C1O GGZZISOUXJHYOY-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 229910000378 hydroxylammonium sulfate Inorganic materials 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 210000003127 knee Anatomy 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 238000011272 standard treatment Methods 0.000 description 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 239000012224 working solution Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/42—Bleach-fixing or agents therefor ; Desilvering processes
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Abstract
Description
【発明の詳細な説明】
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
、更に詳しくは漂白定着処理後の水洗処理に代る処理液
を使用する処理方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION A) Industrial Application Field The present invention relates to a method for processing silver halide color light-sensitive materials, and more particularly to a processing method using a processing solution in place of washing with water after bleach-fixing. It is.
口)従来の技術及び解決すべき点
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、安定的に多着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績の処理液を補充液として
補充する方法で行なわれている。近年この補充喰は少量
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
器に回収する東が可能となっている。−力水洗処理は多
1.)の水を使用して行っており、多着の水洗水を使用
する・ISから使用後の排水を容器に回収する・K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°11となる。更に多;11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F、)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、−
L現像処理の様に夕晴の写真を処理するのであればその
目的を十分にはたす、今日の様に自動現像機を使用して
多聞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は利用出来、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沈水
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。この様な自動現像機を
使用する場合水洗の前の工程である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濃度とな
るが、本来分解はしない漂白定着液でも、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なうためには
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1tで水洗水が使用され排出水となるまで水洗槽に
滞留する時間が艮くなり微生物の発生があり画像にイ・
1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・IS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。(1) Conventional techniques and points to be solved Silver halide color light-sensitive materials are processed using a bleach-fix solution containing iron salts and thiosulfates of aminopolycarboxylic acids after color development, and then washed with running water. When processing silver halide color light-sensitive materials in this way, one way to stably process multiple deposits is to use a replenisher to add the necessary amount of processing solution depending on the amount of light-sensitive material to be processed. This is done as a supplementary method. In recent years, this replenishment has become smaller and the amount of processing liquid discharged after use is also small, making it possible to collect it in a container. -Power washing treatment is often 1. ), and a large amount of washing water is used. - Drainage from the IS is collected in a container after use. - K is not possible, and automatic development is used to process silver halide color light-sensitive materials. The machine requires facilities for water supply and drainage after use, and this facility limits the installation location of the automatic developing machine. Furthermore, since the washing water used in step 11 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. For this reason, various methods have been tried.
One such method is the cascade method, 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 washing water of low F, ), which has been known for a long time. . It is true that this method allows efficient washing with water,
If you are processing a photograph of a sunset as in the case of L-processing, it will serve the purpose well. It can be used as a washing method, and it has many washing tanks. In this washing tank, submerged water is added from the last washing tank, and the overflowing water 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 bleach-fix solution, which is a step before washing, is carried by the photosensitive material being processed and reaches a constant concentration in each washing tank, but even though the bleach-fix solution does not decompose, In some of the washing tanks, the composition is unbalanced and decomposition occurs, which causes deterioration of image quality.In order to perform efficient washing with as little washing water as possible, it is necessary to connect the washing tanks in a cascade. It would be better to increase the number of washing tanks, but with 1 ton of washing water used, the time it takes to stay in the washing tank until it becomes waste water increases, causing the generation of microorganisms and causing problems with the image.
At the same time, the disadvantage of increasing the number of washing tanks in order to increase washing efficiency is becoming apparent.IS also has the disadvantage of increasing the space of the automatic processor facility.
この様な欠点を無くすための新しい方法が要望されてお
り、その方法として2〜341g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+lGで排出される液酸の減少
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
た少数の処理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。特開昭58−18631にはこ
の様な漂白定着に統〈水洗に代り、処理液を使用してハ
ロゲン化銀感光材料を処理する方法が記載されている。There is a need for a new method to eliminate these drawbacks, and one of the objectives has been achieved by cascading 2-341g washing tanks and processing with a small amount of processing solution that is replenished. In addition, in order to obtain a high-quality image and an image with sufficient stability, a processing solution is used, and an automatic processor with a total of fewer processing tanks reduces space and uses a small amount of processing solution. Since the amount of liquid acid discharged is reduced, it becomes possible to collect it in a container, and there is no need to install water supply and drainage for washing, and there are no restrictions on the location of the facility. In processing with such a small number of processing tanks, it is necessary to obtain high-quality images, to have sufficiently stable images, and to improve the stability of the treated water and the processing efficiency. JP-A-58-18631 describes a method for processing silver halide light-sensitive materials using a processing solution instead of washing with water for bleach-fixing.
自動現像機を使用して効率良く多暖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記載されている有機ホスホン酸
を使用した場合、使用液としてストックされている処理
液は日数の経過に従い白色の不溶物が発生し、この状態
で使用した場合1本来の効果は得られず更に安定性の高
い処理液が望まれている。In order to continue processing silver halide photosensitive materials efficiently and in a stable manner using an automatic processor, the processing solution used must be stable, and the organic phosphonic acids listed above were used. In this case, the processing solution that is stocked as a working solution generates white insoluble matter as the days pass, and if it is used in this state, the original effect will not be obtained, and a more stable processing solution is desired. .
二)問題点を解決するための手段
本発明は、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+バの出来るようにしたも
ので、アミノポリカルボン酸鉄塩とチオ硫酸塩から成る
漂白定着液に続く水洗処理に代り使用する処理液は、少
なくともl−ヒドロキシアルキリデン−1,1−ジホス
ホン酸の縮合二Iヨ体を含む処理液を使用する・バを特
徴とする。2) Means for Solving the Problems The present invention relates to a method of using a processing solution instead of washing with water following a bleach-fix solution containing iron salts and thiosulfates of aminopolycarboxylic acids, and its purpose is to It is made of iron aminopolycarboxylic acid salt and thiosulfate, which allows for processing with excellent stability over long-term use, and also improves the stability of processed photographic images. The processing solution used in place of the water washing treatment subsequent to the bleach-fix solution is characterized by the use of a processing solution containing at least a condensed diisomer of l-hydroxyalkylidene-1,1-diphosphonic acid.
ホ)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。E) Examples The present invention will be explained in detail by Examples below, but the embodiments of the present invention are not limited thereto.
実施例1゜
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。Example 1 Commercially available color paper was processed as follows using a small automatic processor.
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。Standard treatment process The composition of each treatment liquid used in this treatment is as follows.
発色現像液
ジエチレングリコール 15.0g
ベンジルアルコール 16、Of
無水亜硫酸ナトリウム 2.5g
臭化カリウム 017g
無水炭酸カリウム 30、Og
M酸ヒドロキシルアミン 3.2g
ヘキサメタン酸ナトリウム 2.Og
3−メチル−4−7ミノーN−エチル
−N−(β−メタンスルフォンアミド
エチル)アンリン硫酸塩 5.5 g水酸化ナトリ
ウム 3.Og
水を加えて l、O1
発色現像補充液
ジエチレングリコール 18.0 gベンジルア
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 30.0 g硫酸ヒドロ
キシルアミン 4. 0 gへキサメタン酸ナト
リウム 2.0g
3−メチル−4−アミノ−N−エチル
−Nl−(β−メタンスルフォンアミドエチル)アンリ
ン硫酸塩 6.8g
水酸化ナトリウム 4. 1 g水を加え
て 1.0 f漂白定着液
チオ硫酸アンモニウム 100.0g
エチレンジアミン
四酢酸鉄ナトリウム 50.0g
エチレンジアミン
四酢酸二ナトリウム 3.0g
無水亜硫酸ナトリウム 15.0g
炭酸ナトリウム 5.Og
水を加えて 1.O見
漂白定着補充液
チオ硫酸アンモニウム 120.0g
エチレンジアミン
四酢酸鉄ナトリウム so、o gエチレンジア
ミン
四酢酸二ナトリウム 4.0g
無水亜硫酸ナトリウム 20.0g
水を加えて 、 l、OfL使用した小型
自動現像機の水洗は独立した2槽の水洗槽をカスケード
で連結し、又処理するに当り発色現像及び漂白定着の補
充j4はノ(にlゴ当り320m見で行った。漂白定着
処理に続く処理は次の様に行った。Color developer diethylene glycol 15.0 g Benzyl alcohol 16, Of anhydrous sodium sulfite 2.5 g Potassium bromide 017 g Anhydrous potassium carbonate 30, Of M acid hydroxylamine 3.2 g Sodium hexamethanate 2. Og 3-Methyl-4-7minor N-ethyl-N-(β-methanesulfonamidoethyl)anline sulfate 5.5 g Sodium hydroxide 3. Og Add water l, O1 Color developer replenisher diethylene glycol 18.0 g Benzyl alcohol 20.0 g Anhydrous sodium sulfite 3.0 g Anhydrous potassium carbonate 30.0 g Hydroxylamine sulfate 4. 0 g Sodium hexamethanate 2.0 g 3-Methyl-4-amino-N-ethyl-Nl-(β-methanesulfonamidoethyl)anline sulfate 6.8 g Sodium hydroxide 4. Add 1 g water 1.0 f Bleach-fix ammonium thiosulfate 100.0 g Sodium iron ethylenediaminetetraacetate 50.0g Disodium ethylenediaminetetraacetate 3.0g Anhydrous sodium sulfite 15.0g Sodium carbonate 5. Og Add water 1. Bleach-fixing replenisher ammonium thiosulfate 120.0g Sodium iron ethylenediaminetetraacetate so,og Disodium ethylenediaminetetraacetate 4.0g Anhydrous sodium sulfite 20.0g Add water, l, Washing of a small automatic processor using OfL. Two independent washing tanks were connected in a cascade, and replenishment of color development and bleach-fixing during processing was carried out at a distance of 320 m per wash.The processing following the bleach-fixing process was as follows. I went to
(1)感光材料trn”’+す129.の水洗(これま
での方法)
(2)感光材料1rn”’Sす0.6文の水洗(水洗本
縫の方法)
(3)感光材料1ITW′当り0.6文の処理液を使用
(本発明)
この処理液の組成は次の通りである。(1) Washing the photosensitive material trn'''+su129. with water (previous method) (2) Washing the photosensitive material 1rn'''S0.6 with water (method of washing with water and lockstitching) (3) Photosensitive material 1ITW' A processing solution of 0.6 centimeters per sample was used (in accordance with the present invention). The composition of this processing solution was as follows.
処理液(I)
l−ヒドロキシアルキリデン
−1,1−ジホスホン1%+ 4.0g水酸化カリウ
ム 1.5 g水を加えて
1.0 1処理液(II )
1−ヒドロキシアルキリデン
−1,l−ジホスホン酸 2、Og
綜合工場体
水酸化カリウム 1.5g
水を加えて 1.0 立前記処理方
法及び処理液を使用して、市販カラーベーパーを150
rn’処理した結果、漂白定着処迎接の処理液及び水洗
水の状態は、以下の様である。Treatment liquid (I) 1% l-hydroxyalkylidene-1,1-diphosphone + 4.0g potassium hydroxide 1.5g water added
1.0 1 Treatment liquid (II) 1-Hydroxyalkylidene-1,l-diphosphonic acid 2,0g Integrated factory potassium hydroxide 1.5g Add water 1.0 Using the above treatment method and treatment liquid , commercially available color vapor 150
As a result of the rn' treatment, the conditions of the bleach-fix treatment solution and washing water are as follows.
更に、一定置光を与えたカラーペーパーを処理した資料
を太陽光に60日間照射、温度60’C1湿度70%の
恒温恒湿槽中に40日間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マクベ
ス、HD−514である。Furthermore, we compared the durability of images by irradiating colored paper with constant light for 60 days in sunlight and placing it in a constant temperature and humidity chamber at 60'C and 70% humidity for 40 days.The results are as follows. It's like that. The densitometer used for concentration measurement was Macbeth HD-514.
画像のない部分の太陽光照射前後の濃度画像のない部分
の恒温恒湿試験前後の濃度各々、8色光、緑色光、赤色
光で露光し、処理された画像の太陽光照射前後の濃度。The density of the area without an image before and after irradiation with sunlight.The density of the area without an image before and after a constant temperature and humidity test.The density of the image exposed and processed with 8-color light, green light, and red light before and after irradiation with sunlight.
各々、青色光、緑色光、赤色光で露出し処理された画像
の恒温恒湿試験前後の濃度。Density before and after constant temperature and humidity test of images exposed and processed with blue light, green light, and red light, respectively.
BD、青色光濃度
GD、緑色光濃度
HD、赤色光濃度
この結果より、処理方法(1)、(2)は、処理液の汚
染もなく、更に画像汚染もなく、合せて画像劣化も無い
が処理方法(2)は処理液のうち染、画像汚染、画像劣
化があり、本発明の処理方法(3)、処理液(■)はこ
れまでの水洗方法に代えて使用することが分る。BD, blue light density GD, green light density HD, red light density From these results, processing methods (1) and (2) cause no contamination of the processing solution, no image contamination, and no image deterioration. It can be seen that processing method (2) causes dyeing, image staining, and image deterioration in the processing solution, and processing method (3) and processing solution (■) of the present invention can be used in place of the conventional water washing method.
実施例2゜
実施例1の処理方法(3)及び処理液(I)、(II
)を使用して、実施例1と同じ処理を10日間継続した
結果は次の様である。Example 2゜Treatment method (3) and treatment liquids (I) and (II) of Example 1
), the same treatment as in Example 1 was continued for 10 days, and the results are as follows.
画像のない部分の太陽光照射前後の濃度画像のない部分
の恒温恒湿試験前後の濃度BD、青色光濃度
GD、緑色光濃度
RD、赤色光濃度
この結果より、処理方法(3)で処理液(II)を使用
すると、処理液の白濁もなく本発明の方法が優れている
市が分る。Concentration of the area without an image before and after sunlight irradiation Concentration of the area without an image before and after constant temperature and humidity test BD, blue light density GD, green light density RD, red light density Based on these results, processing solution using processing method (3) When (II) is used, it is found that the process of the present invention is superior in that there is no clouding of the treatment liquid.
実施例3
実施例1の処理方法(3)及び発色現像液(補充液)は
実施例1の処理液を使用、漂白定着処理に続く処理液は
次の組成を使用した。Example 3 The processing method (3) of Example 1 and the processing solution of Example 1 were used as the color developing solution (replenisher), and the following composition was used for the processing solution following the bleach-fixing process.
処理液(III)
l−ヒドロキシアルギブリン−1,1−ジホスホン酸縮
合二に体 4.Og水酸化ナトリウA
6.0g氷酢酸 6
.0g水を加えて 1.0交処理液(
IV)
l−ヒドロキシアルキプリン−1,1−ジホスホン酸縮
合二量″体 4,0gホルマリン
2.0m文水酸化アンモニウム 2
、OmJl水を加えて 1.OR又、
上記処理液の使用績は、感光材料1rn’当り0.4立
とし処理方法(4)とした。Treatment liquid (III) l-hydroxyargibulin-1,1-diphosphonic acid condensed diisomer 4. Og sodium hydroxide A
6.0g glacial acetic acid 6
.. Add 0g of water and make 1.0 of the exchange solution (
IV) l-Hydroxyalkypurine-1,1-diphosphonic acid fused dimer 4.0g formalin
2.0m ammonium hydroxide 2
, add OmJl water 1. OR again,
The usage history of the above-mentioned processing liquid was set to 0.4 tert per rn' of the photosensitive material, and processing method (4) was used.
前記処理方法(4)、処理液(m)、(IT)で処理を
行なったものは、処理液の白濁も無く、処理液の汚染、
処理されたペーパーの汚染も無い。Those treated with the treatment method (4), treatment liquid (m), and (IT) had no clouding of the treatment liquid, and no contamination or contamination of the treatment liquid.
There is also no contamination of the treated paper.
特許出願人 中外写真薬品株式会社 、〜ニー 代理人 弁理士 高 橋 三 雄1゛−1−二Patent applicant: Chugai Photo Pharmaceutical Co., Ltd. ,~knee Agent Patent Attorney Miyu Takahashi 1-1-2
Claims (1)
理後少なくとも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
、少なくとも1−ヒドロキシアルキリデン−1,1−ジ
ホスホン酸又はそのアルカリ塩の縮合二量体を含有する
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。Regarding the processing of silver halide color light-sensitive materials, after color development processing, processing is performed with a bleach-fix solution containing at least iron salt of aminopolycarboxylic acid and thiosulfate, and instead of subsequent washing with water, at least 1-hydroxyalkylidene-1, 1. A method for processing a silver halide color light-sensitive material, which comprises using a processing solution containing a condensed dimer of 1-diphosphonic acid or an alkali salt thereof.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2038086A JPS62178263A (en) | 1986-01-31 | 1986-01-31 | Processing method for silver halide color photosensitive material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2038086A JPS62178263A (en) | 1986-01-31 | 1986-01-31 | Processing method for silver halide color photosensitive material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS62178263A true JPS62178263A (en) | 1987-08-05 |
Family
ID=12025433
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2038086A Pending JPS62178263A (en) | 1986-01-31 | 1986-01-31 | Processing method for silver halide color photosensitive material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62178263A (en) |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60220345A (en) * | 1984-04-17 | 1985-11-05 | Konishiroku Photo Ind Co Ltd | Method for processing silver halide color photosensitive material |
JPS60241053A (en) * | 1984-05-16 | 1985-11-29 | Konishiroku Photo Ind Co Ltd | Treatment of silver halide color photographic sensitive material |
JPS60263151A (en) * | 1984-06-12 | 1985-12-26 | Konishiroku Photo Ind Co Ltd | Treatment of silver halide color photographic sensitive material |
JPS6111745A (en) * | 1984-06-26 | 1986-01-20 | Fuji Photo Film Co Ltd | Treatment of color silver halide photographic sensitive material |
-
1986
- 1986-01-31 JP JP2038086A patent/JPS62178263A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60220345A (en) * | 1984-04-17 | 1985-11-05 | Konishiroku Photo Ind Co Ltd | Method for processing silver halide color photosensitive material |
JPS60241053A (en) * | 1984-05-16 | 1985-11-29 | Konishiroku Photo Ind Co Ltd | Treatment of silver halide color photographic sensitive material |
JPS60263151A (en) * | 1984-06-12 | 1985-12-26 | Konishiroku Photo Ind Co Ltd | Treatment of silver halide color photographic sensitive material |
JPS6111745A (en) * | 1984-06-26 | 1986-01-20 | Fuji Photo Film Co Ltd | Treatment of color silver halide photographic sensitive material |
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