JPH025048A - Color photographic developer and development of color photographic material - Google Patents
Color photographic developer and development of color photographic materialInfo
- Publication number
- JPH025048A JPH025048A JP1040461A JP4046189A JPH025048A JP H025048 A JPH025048 A JP H025048A JP 1040461 A JP1040461 A JP 1040461A JP 4046189 A JP4046189 A JP 4046189A JP H025048 A JPH025048 A JP H025048A
- Authority
- JP
- Japan
- Prior art keywords
- developer
- color photographic
- development
- salt
- color
- 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 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims abstract description 12
- 150000003839 salts Chemical class 0.000 claims abstract description 9
- 239000003963 antioxidant agent Substances 0.000 claims abstract description 6
- 230000003078 antioxidant effect Effects 0.000 claims abstract description 5
- 238000000034 method Methods 0.000 claims description 23
- 239000000839 emulsion Substances 0.000 claims description 13
- -1 silver halide Chemical class 0.000 claims description 12
- 229910052709 silver Inorganic materials 0.000 claims description 9
- 239000004332 silver Substances 0.000 claims description 9
- 239000000126 substance Substances 0.000 claims description 7
- 239000007864 aqueous solution Substances 0.000 claims description 3
- 150000002500 ions Chemical class 0.000 abstract description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 239000000243 solution Substances 0.000 description 5
- 241001479434 Agfa Species 0.000 description 3
- 229920001174 Diethylhydroxylamine Polymers 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- FVCOIAYSJZGECG-UHFFFAOYSA-N diethylhydroxylamine Chemical compound CCN(O)CC FVCOIAYSJZGECG-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 235000019445 benzyl alcohol Nutrition 0.000 description 2
- 238000004061 bleaching Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- KRTDQDCPEZRVGC-UHFFFAOYSA-N 2-nitro-1h-benzimidazole Chemical compound C1=CC=C2NC([N+](=O)[O-])=NC2=C1 KRTDQDCPEZRVGC-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 150000003568 thioethers Chemical class 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
- G03C7/407—Development processes or agents therefor
- G03C7/413—Developers
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】
大部分の感光性ハロゲン化銀記録材料に対して標準化さ
れた現像法がある。この方法においては、例えば、イエ
ローカプラーを含む少なくとも１つの青感性ハロゲン化
銀に乳剤層と、マゼンタカプラーを含む少なくとも１つ
の緑感性ハロゲン化銀乳剤層と、シアンカプラーを含む
少なくとも１つの赤感性ハロゲン化銀乳剤層から成る透
明なカラネガを使用して、カラーネガティブペーパー上
にカラー反射コピーを生成させるために、任意の由来の
写真記録材料をそのタイプに応じて処理することかでき
る。DETAILED DESCRIPTION OF THE INVENTION There are standardized development methods for most photosensitive silver halide recording materials. In this method, for example, at least one blue-sensitive silver halide emulsion layer containing a yellow coupler, at least one green-sensitive silver halide emulsion layer containing a magenta coupler, and at least one red-sensitive silver halide emulsion layer containing a cyan coupler are provided. Using a transparent color negative consisting of a silveride emulsion layer, photographic recording material of any origin can be processed, depending on its type, to produce color reflective copies on color negative paper.
カラーネガティブペーパーの処理に世界中で使用されて
いるアグファ・カラー・プロセスＡＰ９２としても知ら
れているＥＰ−２法において、像が形成されるように露
光されたカラーネガティブペーパーは、カラー現像、漂
白、定着、洗浄及び乾燥に付される。漂白及び定着は漂
白定着により置き換えられてもよく、そして洗浄は安定
化により置き換えられてもよい。In the EP-2 method, also known as Agfa Color Process AP92, which is used worldwide for processing color negative papers, color negative papers that have been imagewise exposed are subjected to color development, bleaching, , fixing, washing and drying. Bleaching and fixing may be replaced by bleach-fixing and washing may be replaced by stabilizing.
カラー現像に必要な時間は２１０秒である。この時間を
短縮するために相当な努力がなされたが、低い割合の塩
化物（〈２０モル％Ｃ１）しか含まない主として臭化銀
乳剤から成る当業界で普通に使用されるカラーネガティ
ブペーパーで所望の結果を達成することができる新しい
方法は、当業界ではこれまで確立されていない。The time required for color development is 210 seconds. Although considerable efforts have been made to reduce this time, it is not desirable for color negative papers commonly used in the industry, consisting primarily of silver bromide emulsions containing only a low proportion of chloride (<20 mol% C1). No new method has hitherto been established in the art that can achieve this result.
最近導入された唯一の方法は、現像時間が４５秒である
が、この方法は、主として塩化銀乳剤から成り（〉９５
モル％ＣＩ）そして種々の現像剤組成（ＲＡ−４法）を
使用するカラーネガティブペーパーを必要とする。この
方法は、塩化物乳剤は臭化物乳剤よりも速く現像させる
ことができるという公知の事実を利用している。The only recently introduced method has a development time of 45 seconds, but this method consists primarily of a silver chloride emulsion (>95
mole % CI) and require color negative papers using various developer compositions (RA-4 method). This method takes advantage of the known fact that chloride emulsions can be developed faster than bromide emulsions.
本発明の目的は、高い塩化物含有率を持ったカラーネガ
ティブペーパーについて現像時間を更に減少させること
ができる写真プロセスを提供することである。It is an object of the present invention to provide a photographic process in which development times can be further reduced for color negative papers with high chloride content.
この問題は、成る濃度の公知の現像剤成分の組み合わせ
により特徴付けられる現像剤を使用することにより解決
されることが今回見出だされた。It has now been found that this problem is solved by using a developer characterized by a combination of known developer components in concentrations of:
故に、本発明は、使用する用意の整った１ｌの水性溶液
中に、
ａ）下記式
に相当する現像剤４−１５ｇ又は対応する量のその塩（
ＣＤ３）と、
ｂ）下記式
に相当する現像剤０−２．０ｇ又は対応する量のその塩
（ＣＤ４）と、
Ｃ）特にに３ＰＯ，又はに２ＨＰＯ，の形態のＰＯ４３
−イオン８−３５ｇと、
ｄ）酸化防止剤少なくとも０．２ｇと、ｅ）ＫＣｌ、０
．５−５、Ｏｇと、
ｆ）ＫＢｒ、０−０．５ｇと、
他の慣用の成分を含みそして１０．４−１２゜９のｐＨ
に調節されたカラー写真現像液に関する。The invention therefore provides for the following: a) 4-15 g of a developer corresponding to the following formula or a corresponding amount of its salt (
CD3); b) 0-2.0 g of a developer corresponding to the following formula or a corresponding amount of its salt (CD4); and C) PO43, especially in the form of 3PO or 2HPO.
- 8-35 g of ions; d) at least 0.2 g of antioxidant; e) KCl, 0
．． 5-5, Og, f) KBr, 0-0.5g and other conventional ingredients and a pH of 10.4-12°9.
This invention relates to a color photographic developer adjusted to
この現像液は臭化物を含まないことが好ましい。Preferably, this developer is bromide-free.
光学的明色化剤（ｏｐｔｉｃａｌ ｂｒｉｇｈｔｎｅｒ
）、ポリアルキレングリコール、表面活性剤、水軟化剤
及び安定剤、例えば複素環式メルカプト化合物又はニト
ロベンゾイミダゾール及びｐＨを必要な値に調節する物
質を追加ｐ成分として使用することができる。この現像
液はベンジルアルコール２５ｇも含むことができるが、
５ｇ以下のベンジルアルコールを使用することが好まし
く、ベンジルアルコールを含まない現像液を使用するの
がなお一層好ましい。optical brightner
), polyalkylene glycols, surfactants, water softeners and stabilizers such as heterocyclic mercapto compounds or nitrobenzimidazole and substances which adjust the pH to the required value can be used as additional p-components. This developer can also contain 25g of benzyl alcohol,
It is preferred to use up to 5 g of benzyl alcohol, and it is even more preferred to use a benzyl alcohol-free developer.
適当な酸化防止剤の例は、ヒドロキシルアミン、ジエチ
ルヒドロキシルアミン及びサルファイドであり、これら
は５ｇまでの量で使用するのが好ましい。Examples of suitable antioxidants are hydroxylamine, diethylhydroxylamine and sulfides, which are preferably used in amounts up to 5 g.
使用する用意の整った溶液は、個々の成分又はいわゆる
濃縮物から調製することができる。この濃縮物には個々
の成分が実質的により高い濃度で溶解している。この濃
縮物は、いわゆる更新液（ｒｅｐｌｅｎｉｓｈｅｒ）の
調製に使用することができるように調節される。この更
新液は、即ち、使用の用意の整った溶液よりも幾分高い
濃度の個々の成分を含有している溶液であり、この溶液
は、一方では、更に希釈すること及び開始剤、好ましく
はＫＣＩの添加により使用する用意の整った溶液に構成
することができ、他方、連続的に使用中の現像液に添加
して、現像により消費された薬品又はオーバーフローに
よりもしくは現像した材料と共に現像液から運び出され
た薬品を補充することかできる。Solutions ready for use can be prepared from the individual components or from so-called concentrates. In this concentrate, the individual components are dissolved in substantially higher concentrations. This concentrate is conditioned so that it can be used for the preparation of so-called replenishers. This renewal liquid is thus a solution containing a somewhat higher concentration of the individual components than in the solution ready for use, which on the one hand requires further dilution and an initiator, preferably The addition of KCI can make up the solution ready for use, while it can be continuously added to the developer in use to remove chemicals consumed by development or by overflow or together with the developed material from the developer. It is possible to replenish the medicines that have been carried out.
塩化物イオンは普通は調製したばかりの現像液以外に対
しては添加する必要はない。その理由は、塩化物イオン
は現像プロセスにより写真材料から放出されるからであ
る。Chloride ions usually do not need to be added to anything other than freshly prepared developer solutions. The reason is that chloride ions are released from the photographic material by the development process.
本発明に従う現像液組成物は高度に活性であるので、例
えばＫＣＩの現像抑制作用に容易に打ち勝って、オーバ
ーフローなしの補充か可能である。Since the developer composition according to the invention is highly active, it easily overcomes the development-inhibiting effect of, for example, KCI and allows replenishment without overflow.
更に、本発明は、本発明に従う現像液を使用して、感光
性乳剤層が少なくとも８０モル％、好ましくは少なくと
も９５モル％の塩化物含有率を持ったハロゲン化銀を含
有する露光した写真材料を現像する方法、特に、現像が
最も長くて４０秒、好ましくは２０秒以下の範囲内で終
了する現像方法に関する。Furthermore, the present invention provides for exposing photographic materials in which the light-sensitive emulsion layer contains silver halide with a chloride content of at least 80 mol%, preferably at least 95 mol%, using the developer according to the invention. It relates to a method for developing, particularly a method in which development is completed within a maximum of 40 seconds, preferably within 20 seconds.
所定の量の現像剤ａ）及びｂ）の範囲内で、ａ）＝ｂ）
の重量比は最適の光堅ろう度のためには４：１より大き
いことが好ましい。実際には、現像物質ａ）のみを使用
することが好ましい。Within a given amount of developer a) and b), a)=b)
The weight ratio of is preferably greater than 4:1 for optimal light fastness. In practice it is preferred to use only developer substance a).
本発明に従う現像剤によって、感光性乳剤層が少なくと
も８０モル％の塩化物含有率を持ったハロゲン化銀を含
有するカラー写真ネガティブペパーを、３８°Ｃ以下の
温度で１５秒の範囲内に現像して１．ＲＡ−４プロセス
により同じカラーネガティブペーパーに対して４５秒で
得られる像に匹敵する優れた品質の像を生成させること
ができる。Color photographic negative paper whose light-sensitive emulsion layer contains silver halide with a chloride content of at least 80 mol % is developed by the developer according to the invention within 15 seconds at a temperature below 38°C. Then 1. The RA-4 process can produce images of excellent quality comparable to those obtained in 45 seconds on the same color negative paper.
特に、色の光堅ろう度の損失はみられない。In particular, no loss of color light fastness is observed.
現像温度を上げる場合には、５秒までの現像時間を使用
することができる。If the development temperature is increased, development times of up to 5 seconds can be used.
実施例１
高い塩化物含有率を持った市販のカラーペーパ［約９９
．５モル％ＣＩ＝及び０．５モル％Ｂｒ−を含有する乳
剤を有するコダック２００１（Ｋｏｄａｋ ２００１）
又はアグファカラータイプ９ （Ａｇｆａ ｃ。Example 1 Commercially available color paper with high chloride content [approx.
．． Kodak 2001 with emulsion containing 5 mol% CI= and 0.5 mol% Br−
or Agfa color type 9 (Agfa c.
ｆｏｕｒ ｔｙｐｅ ９）を像が形成されるように露光
し、下記の現像剤で現像しそして慣用の方法で漂白し、
定着し、洗浄し、乾燥する。この方法は、最小デンシテ
ィ−１γ−１値、γ−２値及び最大デンシティ−に関し
て個々のタイプに合わせて調節されＩこ。four type 9), imagewise exposed to light, developed with the developer described below and bleached in a conventional manner,
Fix, wash and dry. This method is adjusted to the individual type with respect to the minimum density-1 γ-1 value, the γ-2 value and the maximum density.
水性現像剤は１リツトル当たり下記の物質：ベンジルア
ルコール１５ｍＬ
ジエチレングリコール８．５ｍＬ
ジエチルヒドロキシルアミンｉ、ｏｇ。The aqueous developer contains the following substances per liter: benzyl alcohol 15 mL diethylene glycol 8.5 mL diethyl hydroxylamine i.og.
ＣＤ−３，１１，０ｇ。CD-3, 11, 0g.
Ｋ２ＳＯ３，１，ｏｇ。K2SO3,1,og.
Ｋ３ＰＯ，，４４ｇ１ ＫＣＩ、１．２ｇ。K3PO,,44g1 KCI, 1.2g.
及び通常の量の表面活性剤、光学的明色化剤、安定剤及
び水軟化剤を含有しそしてｐＨ１１，６に調節される。and the usual amounts of surfactants, optical brighteners, stabilizers and water softeners and adjusted to a pH of 11.6.
現像時間＝１５秒／３８°Ｃ０
比較実施例（ＲＡ−４プロセス）
下記の組成ニ
トリエタノールアミンｌ１ｍ（２、
ジエチルヒドロキシルアミンの８５％水性溶液５ｍ１２
、
Ｋ２ＳＯ３０゜３ｇ１
ＣＤ−３、５ｇ。Development time = 15 seconds / 38 ° C0 Comparative example (RA-4 process) The following composition Nitriethanolamine 1 ml (2, 85% aqueous solution of diethylhydroxylamine 5 ml 12
, K2SO30°3g1 CD-3, 5g.
Ｋ２ＣＯ２２５ｇ１ ＫＣＩ 、 ２．３ｇ。K2CO225g1 KCI, 2.3g.
及び通常の量の表面活性剤、光学的明色化剤、安定剤及
び水軟化剤、
の現像剤を使用して、実施例１を繰り返す。この現像液
はＫＯＨでｐＨ１ｏ、■に調節される。Example 1 is repeated using a developer of: and the usual amounts of surfactants, optical brighteners, stabilizers and water softeners. This developer was adjusted to pH 1o, ■ with KOH.
現像時間：４５秒／３５°Ｃ８
実施例２
ベンジルアルコール又はジエチレングリコールを使用し
ないで、実施例１を繰り返す。Development time: 45 seconds/35°C8 Example 2 Example 1 is repeated without using benzyl alcohol or diethylene glycol.
現像時間：１５秒／３８°Ｃ０ 下記の最大デンシティ−が得られる。Development time: 15 seconds/38°C0 The following maximum densities are obtained:
実施例１ 比較実施例 実施例２
イエロー ２４２ ２４３ ２４
０マジエンタ ２７３ ２４７ ２６８
シアン ２８４ ２４６ ２７１本
発明の主なる特徴及び態様は以下のとおりである。Example 1 Comparative Example Example 2 Yellow 242 243 24
0 magenta 273 247 268
Cyan 284 246 271 The main features and aspects of the present invention are as follows.
１、使用する用意の整ったｌｏ、の水性溶液中に、ａ）
下記式
に相当する現像剤４
１５ｇ又は対応する量のそ
め塩（ＣＤ３）と、
ｂ）下記式
に相当する現像剤０−２．０ｇ又は対応する量のその塩
（ＣＤ４）と、
ｃ）Ｐｏ、３−イオン８−３５ｇと、
ｄ）酸化防止剤少なくとも０．２ｇと、ｅ）ＫＣｌ、０
．５−５．０ｇと、
ｆ）ＫＢｒ、ＯＯ−５ｇと、
他の慣用の成分を含みそして１０．４−１２゜９のｐＨ
に調節されたカラー写真現像液。1. In an aqueous solution of lo ready for use, a)
15 g of developer 4 corresponding to the following formula or a corresponding amount of some salt (CD3); b) 0-2.0 g of developer corresponding to the following formula or a corresponding amount of its salt (CD4); c) Po , 8-35 g of 3-ion, d) at least 0.2 g of antioxidant, e) KCl, 0
．． f) KBr, OO-5g and other conventional ingredients and a pH of 10.4-12°9.
Color photographic developer adjusted to
２．８）：ｂ）の重量比が４＝１より大きい上記ｌに記
載のカラー写真現像液。2. The color photographic developer according to item 1 above, wherein the weight ratio of 8):b) is greater than 4=1.
３、現像物質ｂ）を含まないことを特徴とする上記１に
記載のカラー写真現像液。3. The color photographic developer as described in 1 above, characterized in that it does not contain developing substance b).
４、ベンジルアルコールを含まないことを特徴とする、
上記１に記載のカラー写真現像液。4. Characterized by not containing benzyl alcohol,
The color photographic developer described in 1 above.
５、感光性乳剤層が少なくとも８０モル％の塩化物含有
率を有するハロゲン化銀粒子を含有する露光したカラー
写真材料の現像方法において、上記１に記載の現像液を
使用することを特徴とする方法。5. A method for developing an exposed color photographic material in which the light-sensitive emulsion layer contains silver halide grains having a chloride content of at least 80 mol %, characterized by using the developer described in 1 above. Method.
６、現像を多くても４０秒で完了させることを特徴とす
る上記５に記載の現像方法。6. The developing method as described in 5 above, wherein the development is completed in 40 seconds at most.
７、現像を多くても２０秒で完了させることを特徴とす
る上記５に記載の現像方法。7. The developing method as described in 5 above, characterized in that the development is completed in 20 seconds at most.
８、ハロゲン化銀粒子か少なくとも９５モル％の塩化物
を含有することを特徴とする上記５に記載の現像方法。8. The developing method as described in 5 above, wherein the silver halide grains contain at least 95 mol % of chloride.
Claims (1)
ＣＤ３）と、 ｂ）下記式 ▲数式、化学式、表等があります▼ に相当する現像剤０−２．０ｇ又は対応する量のその塩
（ＣＤ４）と、 ｃ）ＰＯ＿４＾３＾−イオン８−３５ｇと、 ｄ）酸化防止剤少なくとも０．２ｇと、 ｅ）ＫＣｌ、０．５−５．０ｇと、 ｆ）ＫＢｒ、０−０．５ｇと、 他の慣用の成分を含みそして１０．４−１２．９のｐＨ
に調節されたカラー写真現像液。２、感光性乳剤層が少
なくとも８０モル％の塩化物含有率を有するハロゲン化
銀粒子を含有する露光したカラー写真材料の現像方法に
おいて、特許請求の範囲第１項に記載の現像液を使用す
ることを特徴とする方法。[Claims] 1. In 1 liter of aqueous solution ready for use, a) 4-15 g of a developer corresponding to the following formula ▲ where there is a mathematical formula, chemical formula, table, etc. ▼ or a corresponding amount of its salt; (
CD3), b) 0-2.0 g of developer corresponding to the following formula ▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ or the corresponding amount of its salt (CD4), and c) PO_4^3^- ion 8- d) at least 0.2 g of antioxidant; e) KCl, 0.5-5.0 g; f) KBr, 0-0.5 g; and 10.4- pH of 12.9
Color photographic developer adjusted to 2. In a method for developing an exposed color photographic material in which the light-sensitive emulsion layer contains silver halide grains having a chloride content of at least 80 mol %, the developer according to claim 1 is used. A method characterized by:
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3805699.2 | 1988-02-24 | ||
| DE3805699A DE3805699A1 (en) | 1988-02-24 | 1988-02-24 | PHOTOGRAPHIC COLOR DEVELOPER SOLUTION AND METHOD FOR DEVELOPING A COLOR PHOTOGRAPHIC MATERIAL |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH025048A true JPH025048A (en) | 1990-01-09 |
Family
ID=6348015
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1040461A Pending JPH025048A (en) | 1988-02-24 | 1989-02-22 | Color photographic developer and development of color photographic material |
Country Status (3)
| Country | Link |
|---|---|
| EP (1) | EP0330035B1 (en) |
| JP (1) | JPH025048A (en) |
| DE (2) | DE3805699A1 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0296143A (en) * | 1988-10-03 | 1990-04-06 | Fuji Photo Film Co Ltd | Method for processing silver halide color photographic sensitive material |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8804606D0 (en) * | 1988-02-26 | 1988-03-30 | Kodak Ltd | Method & apparatus for processing photographic colour materials |
| JPH087418B2 (en) * | 1988-10-03 | 1996-01-29 | 富士写真フイルム株式会社 | Processing method of silver halide color photographic light-sensitive material |
| JP2949879B2 (en) * | 1991-02-20 | 1999-09-20 | コニカ株式会社 | Processing method of silver halide color photographic light-sensitive material |
| DE4114481A1 (en) * | 1991-05-03 | 1992-11-05 | Agfa Gevaert Ag | ENVIRONMENTALLY IMPROVED DEVELOPMENT PROCESS FOR PHOTO MATERIALS AND SUITABLE DEVELOPER SOLUTION |
| US7172854B2 (en) | 2003-11-10 | 2007-02-06 | Konica Minolta Photo Imaging, Inc. | Photographic color developer solution and processing method by use thereof |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5895345A (en) * | 1981-12-01 | 1983-06-06 | Konishiroku Photo Ind Co Ltd | Formation of dye image |
| FR2554935A1 (en) * | 1983-11-15 | 1985-05-17 | Kis France Sa | COMPOSITION TO REVEAL COLOR PHOTOGRAPHS |
| CA1314424C (en) * | 1986-01-24 | 1993-03-16 | Sheridan E. Vincent | Photographic color developing compositions which are especially useful with high chloride photographic elements |
-
1988
- 1988-02-24 DE DE3805699A patent/DE3805699A1/en not_active Withdrawn
-
1989
- 1989-02-13 DE DE8989102423T patent/DE58904034D1/en not_active Expired - Fee Related
- 1989-02-13 EP EP89102423A patent/EP0330035B1/en not_active Expired - Lifetime
- 1989-02-22 JP JP1040461A patent/JPH025048A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0296143A (en) * | 1988-10-03 | 1990-04-06 | Fuji Photo Film Co Ltd | Method for processing silver halide color photographic sensitive material |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0330035A2 (en) | 1989-08-30 |
| EP0330035A3 (en) | 1989-12-06 |
| DE3805699A1 (en) | 1989-09-07 |
| DE58904034D1 (en) | 1993-05-19 |
| EP0330035B1 (en) | 1993-04-14 |
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