JPH02298945A - Processing device for silver halide photographic sensitive material - Google Patents
Processing device for silver halide photographic sensitive materialInfo
- Publication number
- JPH02298945A JPH02298945A JP11959289A JP11959289A JPH02298945A JP H02298945 A JPH02298945 A JP H02298945A JP 11959289 A JP11959289 A JP 11959289A JP 11959289 A JP11959289 A JP 11959289A JP H02298945 A JPH02298945 A JP H02298945A
- Authority
- JP
- Japan
- Prior art keywords
- silver halide
- halide photographic
- tank
- sensitive material
- photographic sensitive
- 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 35
- -1 silver halide Chemical class 0.000 title claims abstract description 14
- 229910052709 silver Inorganic materials 0.000 title claims abstract description 11
- 239000004332 silver Substances 0.000 title claims abstract description 11
- 239000011347 resin Substances 0.000 claims abstract description 13
- 229920005989 resin Polymers 0.000 claims abstract description 13
- 238000005406 washing Methods 0.000 claims description 4
- 239000007788 liquid Substances 0.000 abstract description 2
- 230000007704 transition Effects 0.000 abstract description 2
- 238000001035 drying Methods 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 239000007864 aqueous solution Substances 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 108010010803 Gelatin Proteins 0.000 description 5
- 229920000159 gelatin Polymers 0.000 description 5
- 239000008273 gelatin Substances 0.000 description 5
- 235000019322 gelatine Nutrition 0.000 description 5
- 235000011852 gelatine desserts Nutrition 0.000 description 5
- 238000010586 diagram Methods 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 239000011241 protective layer Substances 0.000 description 3
- 238000004904 shortening Methods 0.000 description 3
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 238000003672 processing method Methods 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- GGZHVNZHFYCSEV-UHFFFAOYSA-N 1-Phenyl-5-mercaptotetrazole Chemical compound SC1=NN=NN1C1=CC=CC=C1 GGZHVNZHFYCSEV-UHFFFAOYSA-N 0.000 description 1
- BDKLKNJTMLIAFE-UHFFFAOYSA-N 2-(3-fluorophenyl)-1,3-oxazole-4-carbaldehyde Chemical compound FC1=CC=CC(C=2OC=C(C=O)N=2)=C1 BDKLKNJTMLIAFE-UHFFFAOYSA-N 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- 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 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- XYXNTHIYBIDHGM-UHFFFAOYSA-N ammonium thiosulfate Chemical compound [NH4+].[NH4+].[O-]S([O-])(=O)=S XYXNTHIYBIDHGM-UHFFFAOYSA-N 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- OKBBUTOWYNETBD-UHFFFAOYSA-L disodium 2-[2-[bis(carboxymethyl)amino]ethyl-(carboxymethyl)amino]acetate acetate Chemical compound C(CN(CC(=O)[O-])CC(=O)[O-])N(CC(=O)O)CC(=O)O.[Na+].[Na+].C(C)(=O)O OKBBUTOWYNETBD-UHFFFAOYSA-L 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- BHZRJJOHZFYXTO-UHFFFAOYSA-L potassium sulfite Chemical compound [K+].[K+].[O-]S([O-])=O BHZRJJOHZFYXTO-UHFFFAOYSA-L 0.000 description 1
- 235000019252 potassium sulphite Nutrition 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 229940087562 sodium acetate trihydrate Drugs 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 229960000999 sodium citrate dihydrate Drugs 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000012224 working solution Substances 0.000 description 1
Landscapes
- Photographic Processing Devices Using Wet Methods (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明はハロゲン化銀写真感光材料の処理装置に関し、
詳しくは印刷製版感光材料用に適した自動現像機に関す
る。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a processing apparatus for silver halide photographic materials,
More specifically, the present invention relates to an automatic processor suitable for printing and plate-making photosensitive materials.
近年、印刷製版業界において、感光材料の処理時間短縮
並びに臭気等の作業環境改善に対する要望は極めて高い
。In recent years, in the printing and plate making industry, there has been an extremely high demand for shortening the processing time of photosensitive materials and improving the working environment such as odor.
現像処理時間を短縮するためには、処理温度を上げるこ
とである程度可能であるが、いくつかの問題も生ずる。Although it is possible to shorten the development processing time to some extent by increasing the processing temperature, several problems arise.
例えば乾燥C:ついては、ある程度以上の温度上昇は印
刷製版用感光材料の重要な特性である処理前後の寸度安
定性に悪影響を及ぼすことは良く知られている。また乾
燥風量を上げることも乾燥時間短縮に有効ではあるが、
送風のための電力の増加、騒音の増大等の別の問題を生
ずる。For example, drying C: It is well known that an increase in temperature above a certain level has an adverse effect on the dimensional stability before and after processing, which is an important characteristic of photosensitive materials for printing plate making. Increasing the drying air volume is also effective in shortening drying time, but
Other problems arise, such as an increase in electric power for blowing air and an increase in noise.
上記問題に対し、本発明の目的は、感光材料の性能、作
業環境、コスト面等を十分考慮した超迅速処理方法を提
供することである。In order to solve the above problems, an object of the present invention is to provide an ultra-rapid processing method that takes into consideration the performance of photosensitive materials, working environment, cost, etc.
本発明の上記目的は、全処理時間(dry to dr
y)が60秒以内であり、かつラインスピードが150
0腸−/霞in以上であるハロゲン化銀写真感光材料用
自動現像機において、現像槽、定着槽、水洗槽の各槽の
出口に、感光材料表面に付着している各処理液を除去す
るため、■エアースリット■薄膜状の軟質樹脂板、の少
なくとも1つ以上を付設した自動現像機を用いることを
特徴とするハロゲン化銀写真感光材料の処理方法により
達成される。The above object of the present invention is to reduce the total processing time (dry to dr.
y) is within 60 seconds and the line speed is 150
In an automatic processor for silver halide photographic light-sensitive materials with a haze level of 0 or more, each processing solution adhering to the surface of the light-sensitive material is removed at the outlet of each of the developing tank, fixing tank, and washing tank. This is achieved by a method for processing silver halide photographic materials, which is characterized by using an automatic developing machine equipped with at least one of the following: (1) air slits (2) and (2) thin film-like soft resin plates.
以下、本発明についてさらに詳細に説明する。The present invention will be explained in more detail below.
本発明において用いられるエアースリットノズルは、ス
リット巾が1Cff1以内で、感光材料面からノズルま
での距離は1cI1以内で平均風速2m/sec以上が
好ましい。さらに乾燥風は感光材料搬送方向に対し逆方
向より風を当てることが感光材料表面の処理液を除去す
るためには好ましい。かつ感光材料の搬送性を考慮して
両サイドにノズルを設置し、バランスをとることと、出
口のローラに近接する所へノズルを設置することが好ま
しい。The air slit nozzle used in the present invention preferably has a slit width of 1 Cff1 or less, a distance from the surface of the photosensitive material to the nozzle of 1 Cff1 or less, and an average wind speed of 2 m/sec or more. Further, it is preferable that the drying air be applied in a direction opposite to the direction in which the photosensitive material is transported in order to remove the processing liquid on the surface of the photosensitive material. In addition, it is preferable to install nozzles on both sides to maintain balance in consideration of the transportability of the photosensitive material, and to install the nozzles near the exit roller.
ノズルの材質は硬質塩化ビニル樹脂、ステンレス等の耐
腐食性のものが適している。Corrosion-resistant materials such as hard vinyl chloride resin and stainless steel are suitable for the nozzle.
また薄膜状の軟質樹脂板を用いる場合は、感光材料面に
対し90″以下、好ましくは45°以下の角度で接する
ことが望ましい。樹脂の素材としてはポリエチレン、ポ
リプロピレン、ポリ塩化ビニル、ポリエチレンテレフタ
レート、3酢酸セルロース、テフロン、イソブチンゴム
、ブタジェンゴム等が用いられるがこれらに限定される
ものではない。In addition, when using a thin film-like soft resin plate, it is desirable that it be in contact with the surface of the photosensitive material at an angle of 90" or less, preferably 45° or less. Materials for the resin include polyethylene, polypropylene, polyvinyl chloride, polyethylene terephthalate, Cellulose triacetate, Teflon, isobutyne rubber, butadiene rubber, etc. are used, but are not limited to these.
処理時間短縮のため、特に乾燥装置への持ち込み水分を
減らすためには、本発明の上記ノズルまたは樹脂板は水
洗槽の出口側に設置することが有効である。処理時間短
縮のためには、乾燥工程の迅速化が最も容易かつ有効で
ある。現像、定着等の時間短縮は性能に対する影響が大
きい。例えばカブリ、色調保存性、残色等の問題が起こ
る可能性が高い。これに対し乾燥工程は水分除去が目的
であるので余分の水分の持ち込みを防ぐことが極めて有
効である。In order to shorten processing time, and particularly to reduce moisture brought into the drying device, it is effective to install the nozzle or resin plate of the present invention on the outlet side of the washing tank. In order to shorten the processing time, it is easiest and most effective to speed up the drying process. Shortening the time for development, fixing, etc. has a large impact on performance. For example, problems such as fogging, color retention, and residual color are likely to occur. On the other hand, since the purpose of the drying process is to remove moisture, it is extremely effective to prevent excess moisture from being introduced.
本発明のノズル及び樹脂板はいずれも各処理槽の出口側
の渡り部分に設ける。Both the nozzle and the resin plate of the present invention are provided at the transition portion on the outlet side of each processing tank.
第1図は本発明におけるエアーノズル方式の場合の説明
図である。同図(a)は、感光材料Sを処理槽の出口側
駆動ロールR8から渡りロールR。FIG. 1 is an explanatory diagram of the air nozzle method according to the present invention. In the same figure (a), the photosensitive material S is transferred from the exit side drive roll R8 of the processing tank to the roll R.
ヘガイドGを介°して誘導するが、その誘導方向に逆に
ノズルNより乾燥風を吹き付けて持ち込み水分の除去を
はかる方式である。また同図(b)ではこのガイドGを
ノズルNと兼用し、ガイドの先端から感光材料Sと逆方
向に風を吹き付ける。In this method, the water is guided through a guide G, but drying air is blown from a nozzle N in the opposite direction of the guide to remove the moisture brought in. Further, in FIG. 2B, this guide G is also used as a nozzle N, and air is blown in the opposite direction to the photosensitive material S from the tip of the guide.
第2図は、樹脂板Pを用いた場合の説明図であるが、第
1図と同様なガイドGに樹脂板Pを感光材料Sをしごく
よう設置した例であって、第2図(c)は1対の場合で
あり、同図(d)は樹脂板を複数設置した例を示した。FIG. 2 is an explanatory diagram when a resin plate P is used, and is an example in which the resin plate P is placed on a guide G similar to that in FIG. 1 so as to squeeze the photosensitive material S. ) shows the case of one pair, and the same figure (d) shows an example in which a plurality of resin plates are installed.
以下、実施例により本発明の効果を例証する。 Hereinafter, the effects of the present invention will be illustrated by examples.
実施例1
28インチ巾の印刷感光材料用自動現像機に水洗槽の出
口側の渡り部分に第1図、及び第2図に示す本発明の水
分除去装置を付設し、下記印刷用感光材料の大全サイズ
(508c■8610cm)を処・理した。Example 1 A water removal device of the present invention shown in FIGS. 1 and 2 was attached to a 28-inch wide automatic developing machine for printing photosensitive materials at the exit side of the washing tank, and the following photosensitive materials for printing were processed. The complete size (508cm x 8610cm) was processed.
処理は下記現像液、定着液により、Dry to Dr
yで45秒〜60秒、ラインスピード1000〜250
0au+/sinの範囲で評価しな。その時の環境条件
は、室温30 ’0湿度80%に設定し、大全サイズの
感光材料を処理した時のwet状態の重量を測定し、さ
らに乾燥後の重量を測定した。このキャリーオーバー(
wet−Dry)量を測定した。その結果を表1に示す
。The processing is done using the following developer and fixer.
y for 45 seconds to 60 seconds, line speed 1000 to 250
Evaluate within the range of 0au+/sin. The environmental conditions at that time were set to a room temperature of 30' and humidity of 80%, and the weight of the photographic material in the wet state after processing the entire size was measured, and the weight after drying was also measured. This carryover (
wet-dry) amount was measured. The results are shown in Table 1.
尚、比較としては本発明の水分除去装置を使用表1
上記表中、Dry to Dry 60秒系で5.5/
g大全以上53秒系で5.l〃
45秒系で4,7//
は乾燥不良を発生しt;。For comparison, the moisture removal device of the present invention was used. In the above table, 5.5/
5. G Daizen or above in 53 seconds. l〃 In the 45 second system, 4,7// caused poor drying.
表1から、本発明の方法を適用した場合にはキャリーオ
ーバー量が著しく低減することができることがわかった
。Table 1 shows that the amount of carryover can be significantly reduced when the method of the present invention is applied.
感光材料の処方
感光材料は、ラテックス下引きを施した厚さ100μm
のポリエチレンテレフタレートの支持体上に、銀量4.
Og/m2となるようにゼラチン3.0g/l12(た
だしゼラチン量1.0g/aFの保護層を含む)を支持
体の反対側にバッキング層として公知の染料を含み、保
護層としてゼラチン1.0g/+”の層を含んでゼラチ
ン量3.0g/m”となるようそれぞれの面に公知の硬
膜剤を添加して塗布乾燥して作成した。尚、乳剤層には
下記化合物(a)、(b)を含有し、乳剤面及びバッキ
ング面の保護層にはそれぞれ不定型シリカのマット剤を
含んでいる。Prescription of photosensitive material The photosensitive material has a thickness of 100 μm with latex undercoating.
on a support of polyethylene terephthalate with an amount of silver of 4.
Gelatin 3.0 g/l12 (including a protective layer with a gelatin amount of 1.0 g/aF) so as to have a gelatin content of 1.0 g/m2, a known dye as a backing layer on the opposite side of the support, and gelatin 1.0 g/l12 as a protective layer. A well-known hardening agent was added to each side of the film so that the gelatin amount was 3.0 g/m'' including a layer of 0 g/+'', and the coating was dried. The emulsion layer contains the following compounds (a) and (b), and the protective layers on the emulsion surface and the backing surface each contain a matting agent of amorphous silica.
(a)
(b)
現像液処方
(組成A)
純水(イオン交換水) 150mQエチ
レンジアミン四酢酸二ナトリウム塩g
ジエチレングリコール 50g亜硫酸カリ
ウム(55%w/v水溶液) 100m12炭酸カ
リウム 509ハイドロキノン
1595−メチルベンゾトリアゾ
ール 200mg1−フェニル−5−メルカプト
テトラゾール30肩9
水酸化カリウム 使用液のpHを10.4にする量臭化
カリウム 4.5g(組成り)
純水(イオン交換水) 3taaジエ
チレングリコール 505Fエチレンジア
ミン四酢酸二ナトリウム塩酢酸(90%水溶液)
0.3m45−二トロインダゾール
110+nl−フェニル−3−ピラゾリドン
500mp現像液の使用時に水500m(!中に
上記組成人,組成りの順に溶かし、lQに仕上げて用い
た。(a) (b) Developer formulation (composition A) Pure water (ion-exchanged water) 150 mQ ethylenediaminetetraacetic acid disodium salt g Diethylene glycol 50 g Potassium sulfite (55% w/v aqueous solution) 100 m12 Potassium carbonate 509 Hydroquinone
1595-Methylbenzotriazole 200mg 1-phenyl-5-mercaptotetrazole 30 shoulders 9 Potassium hydroxide Amount to adjust the pH of the working solution to 10.4 Potassium bromide 4.5g (composition) Pure water (ion exchange water) 3taa diethylene glycol 505F Ethylenediaminetetraacetic acid disodium salt Acetic acid (90% aqueous solution)
0.3m45-nitroindazole
110+nl-phenyl-3-pyrazolidone
When using a 500mp developer, the above compositions were dissolved in 500ml of water in the order of composition and finished to 1Q before use.
定着液処方
(組成A)
チオ硫酸アンモニウム(72.5%V/V水溶液)22
3m+2
亜硫酸ナトリウム 9.59酢酸ナト
リウム・3水塩 34.39硼酸
6.7。Fixer formulation (composition A) Ammonium thiosulfate (72.5% V/V aqueous solution) 22
3m+2 Sodium sulfite 9.59 Sodium acetate trihydrate 34.39 Boric acid
6.7.
クエン酸ナトリウム・2水塩 2.o9酢酸(
90%w/v水溶液) 12.4mff
i(組成り)
純水(イオン交換水) 6m(1硫酸
(50%w/w水溶液) 6.8g硫酸
アルミニウム
Cha、Os換算含量が8.1%w/wの水溶液)20
.0mff
定着液の使用時に水500m(2中に上記組成A1組成
りの順に溶かし、lQに仕上げて用いた。Sodium citrate dihydrate 2. o9 acetic acid (
90% w/v aqueous solution) 12.4 mff
i (composition) Pure water (ion-exchanged water) 6 m (1 sulfuric acid (50% w/w aqueous solution) 6.8 g aluminum sulfate Cha, aqueous solution with an Os equivalent content of 8.1% w/w) 20
.. 0 mff When using the fixer, the above composition A1 was dissolved in 500 m of water (2) in the order of composition, finished to 1 Q, and used.
この定着液のpHは約4.2であった。The pH of this fixer was about 4.2.
本発明により、ハロゲン化銀写真感光材料の性能、作業
環境、コスト面を充分考慮した超迅速処理方法を提供す
ることができた。According to the present invention, it has been possible to provide an ultra-rapid processing method that takes into account the performance, working environment, and cost of silver halide photographic materials.
第1図は、本発明のエアーノズルを用いた場合の説明図
、第2図は、樹脂板を用いた場合の説明図である。
R8:処理槽出口側駆動ロール
R1二渡りロール
S :感光材料FIG. 1 is an explanatory diagram when the air nozzle of the present invention is used, and FIG. 2 is an explanatory diagram when a resin plate is used. R8: Processing tank outlet side drive roll R1 two-way roll S: Photosensitive material
Claims (1)
かつラインスピードが1500mm/min以上である
ハロゲン化銀写真感光材料用自動現像機において、現像
槽、定着槽、水洗槽の各槽の出口に、感光材料表面に付
着している各処理液を除去するため、(1)エアースリ
ット(2)薄膜状の軟質樹脂板、の少なくとも1つ以上
を付設した自動現像機を用いることを特徴とするハロゲ
ン化銀写真感光材料の処理装置。The total processing time (drytodry) is within 60 seconds,
In an automatic developing machine for silver halide photographic light-sensitive materials with a line speed of 1500 mm/min or more, each processing solution adhering to the surface of the light-sensitive material is removed at the outlet of each tank of the developing tank, fixing tank, and washing tank. A processing apparatus for silver halide photographic materials, characterized in that an automatic developing machine equipped with at least one of (1) an air slit and (2) a thin film-like soft resin plate is used.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11959289A JPH02298945A (en) | 1989-05-12 | 1989-05-12 | Processing device for silver halide photographic sensitive material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11959289A JPH02298945A (en) | 1989-05-12 | 1989-05-12 | Processing device for silver halide photographic sensitive material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH02298945A true JPH02298945A (en) | 1990-12-11 |
Family
ID=14765196
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11959289A Pending JPH02298945A (en) | 1989-05-12 | 1989-05-12 | Processing device for silver halide photographic sensitive material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02298945A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0595236A1 (en) * | 1992-10-27 | 1994-05-04 | Fuji Photo Film Co., Ltd. | Method of processing silver halide photographic materials |
-
1989
- 1989-05-12 JP JP11959289A patent/JPH02298945A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0595236A1 (en) * | 1992-10-27 | 1994-05-04 | Fuji Photo Film Co., Ltd. | Method of processing silver halide photographic materials |
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