JPH0564781B2 - - Google Patents

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Publication number
JPH0564781B2
JPH0564781B2 JP60225533A JP22553385A JPH0564781B2 JP H0564781 B2 JPH0564781 B2 JP H0564781B2 JP 60225533 A JP60225533 A JP 60225533A JP 22553385 A JP22553385 A JP 22553385A JP H0564781 B2 JPH0564781 B2 JP H0564781B2
Authority
JP
Japan
Prior art keywords
silver halide
layer
halide photographic
particle size
present
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.)
Expired - Lifetime
Application number
JP60225533A
Other languages
Japanese (ja)
Other versions
JPS6285240A (en
Inventor
Haruhiko Sakuma
Mikio Kawasaki
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.)
Konica Minolta Inc
Original Assignee
Konica Minolta Inc
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 Konica Minolta Inc filed Critical Konica Minolta Inc
Priority to JP22553385A priority Critical patent/JPS6285240A/en
Publication of JPS6285240A publication Critical patent/JPS6285240A/en
Publication of JPH0564781B2 publication Critical patent/JPH0564781B2/ja
Granted legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/76Photosensitive materials characterised by the base or auxiliary layers
    • G03C1/85Photosensitive materials characterised by the base or auxiliary layers characterised by antistatic additives or coatings

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)

Description

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

〔産業上の利用分野〕 本発明はハロゲン化銀写真感光材料に関する。
特に、含フツ素界面活性剤を含有するハロゲン化
銀写真感光材料に関する。 〔従来の技術〕 従来よりハロゲン化銀写真感光材料において、
帯電防止のため含フツ素界面活性剤を用いる技術
が知られている。例えばこのような技術を開示す
るものとして、特開昭54−14224、同50−34233、
同49−46733、同51−32322、同56−19042、同56
−41093、同55−7762、同50−16525、同57−
29691、同57−11341、同54−111330、同56−
34856、特公昭48−43130、同52−25087、同47−
9303、同56−44411、米国特許3775126、同
4292402等がある。しかしこれら従来技術はさま
ざまな保存、使用条件において必ずしもすべての
場合良好な機能を得ることができず、保存条件に
よつては性能変動を来たしてしまうことが多い。
例えば、高温や高湿の条件で保存したりした場
合、性能に変化が生ずることが多い。 〔発明の目的〕 本発明の目的は、上記従来技術の問題点を解決
し、さまざまな保存及び使用条件に対して良好な
帯電防止性能を示すことができるハロゲン化銀写
真感光材料を提供することにある。 〔発明の構成及び作用〕 上記目的は、支持体上にハロゲン化銀乳剤を含
有する層を少なくとも一層有する写真構成層を有
して成るハロゲン化銀写真感光材料において、該
ハロゲン化銀乳剤層を有する側の写真構成層の少
なくともいずれかの層に含フツ素界面活性剤と、
無機アルカリ金属塩と、平均粒径0.8μ以下のポリ
マーラテツクスまたは平均粒径0.8μ以下の無機コ
ロイド物の少なくともいずれかである微粒子とを
含有させ、かつ写真構成層の全バインダーに対
し、 (a) 無機アルカリ金属塩は0.5〜5wt%であり、 (b) ポリマーラテツクスまたは無機コロイド物で
ある微粒子は3wt%以上である ように構成したものによつて、達成される。 即ち、上記構成の本発明のハロゲン化銀写真感
光材料は、例えば高温保存時の帯電防止効果の安
定化や、低湿取扱い時の帯電防止性能の向上など
の、さまざまな条件での帯電防止性能を良好かつ
安定に維持できる。具体的には、高温(例えば30
〜35℃。これはわが国の真夏の高温気温に該当す
る)、高湿(例えば80%RH以上)での帯電防止
効果の劣化が従来の技術におけるより小さく、良
好な作用を示す。また、低湿下例えば30%RHに
おいても、良好な帯電防止効果を維持できる。 本発明の好ましい実施態様にあつては、上記本
発明のハロゲン化銀写真感光材料に分子量300以
上のホリアルキレンオキサイド化合物を全バイン
ダーに対し1〜10wt%以上併用する。これによ
りさらに良好な帯電防止効果が得られる。 また本発明のハロゲン化銀写真感光材料は、製
造時に、各種の層を高速塗布した場合でも、ある
いは塗布層を急速乾燥した場合でも、良好な写真
性能及び帯電防止効果を得やすいものである。例
えばコーテイングスピード100m/min.以上の高
速塗布を行つた場合、及び4分以下の急速乾燥を
行つた場合においても、良好な結果を得やすい。
一般的に急速乾燥を行うと、ポリアルキレンオキ
シド化合物により帯電防止効果を安定して得るこ
とがむずかしくなることがあるが、本発明を用い
るとこの問題をも解決できる。 次に本発明の構成について、更に詳しく述べ
る。 本発明はハロゲン化銀写真感光材料に含有され
る含フツ素界面活性剤としては、各種のものを任
意に使用できる。 本発明の実施の際に使用するのに好適である含
フツ素界面活性剤の代表例には次のものがある。
[Industrial Field of Application] The present invention relates to a silver halide photographic material.
In particular, it relates to a silver halide photographic material containing a fluorine-containing surfactant. [Prior art] Conventionally, in silver halide photographic materials,
A technique using a fluorine-containing surfactant to prevent static electricity is known. For example, Japanese Patent Application Laid-open Nos. 54-14224, 50-34233,
49-46733, 51-32322, 56-19042, 56
-41093, 55-7762, 50-16525, 57-
29691, 57-11341, 54-111330, 56-
34856, Special Publication No. 48-43130, No. 52-25087, No. 47-
9303, 56-44411, U.S. Patent 3775126, 56-44411,
There are 4292402 etc. However, these conventional techniques do not necessarily provide good functionality under various storage and usage conditions, and often result in performance fluctuations depending on the storage conditions.
For example, when stored under high temperature or high humidity conditions, performance often changes. [Object of the Invention] An object of the present invention is to provide a silver halide photographic material that can solve the problems of the prior art described above and exhibit good antistatic performance under various storage and usage conditions. It is in. [Structure and operation of the invention] The above object is to provide a silver halide photographic light-sensitive material comprising a photographic constituent layer having at least one layer containing a silver halide emulsion on a support. a fluorine-containing surfactant in at least one of the photographic constituent layers on the side containing the fluorine-containing surfactant;
( This can be achieved by: a) having an inorganic alkali metal salt content of 0.5 to 5 wt%; and (b) a polymer latex or inorganic colloid fine particles having a content of 3 wt% or more. That is, the silver halide photographic light-sensitive material of the present invention having the above-mentioned structure exhibits antistatic performance under various conditions, such as stabilizing the antistatic effect during high-temperature storage and improving antistatic performance during low-humidity handling. Can be maintained well and stably. Specifically, high temperatures (e.g. 30
~35℃. (This corresponds to the high temperature of midsummer in Japan) and high humidity (for example, 80% RH or higher), the deterioration of the antistatic effect is smaller than in the conventional technology, indicating a good effect. Further, good antistatic effect can be maintained even under low humidity, for example, 30% RH. In a preferred embodiment of the present invention, a polyalkylene oxide compound having a molecular weight of 300 or more is used in an amount of 1 to 10 wt % or more based on the total binder in the silver halide photographic light-sensitive material of the present invention. This provides even better antistatic effect. Further, the silver halide photographic material of the present invention can easily obtain good photographic performance and antistatic effect even when various layers are coated at high speed during production or when the coated layers are rapidly dried. For example, good results are likely to be obtained even when high-speed coating is performed at a coating speed of 100 m/min or more and when rapid drying is performed for 4 minutes or less.
Generally, when rapid drying is carried out, it may be difficult to stably obtain an antistatic effect using a polyalkylene oxide compound, but the present invention can also solve this problem. Next, the configuration of the present invention will be described in more detail. In the present invention, any of various fluorine-containing surfactants can be used as the fluorine-containing surfactant contained in the silver halide photographic light-sensitive material. Representative examples of fluorine-containing surfactants suitable for use in the practice of the present invention include the following.

【表】


OH
【table】


OH

【表】【table】

【表】【table】

〔実施例〕〔Example〕

以下、本発明の実施例について述べる。なお当
然のことではあるが、本発明は以下の実施例によ
り限定されるものではない。 実施例 1 平均粒径0.3μの沃素2モル%、塩素0.2モル%
を含有する単分散塩沃臭化銀の内部核及びその外
側に、沃素40モル%及び臭素60モル%の比率で沃
臭化銀層を設け、0.5μの粒径まで成長させ、ひき
続き沃素1モル%臭素99モル%の比率で0.85μま
で沃臭化銀層を成長させ、やや丸味をおびた14面
体状のハロゲン化銀粒子を得た。 これらの粒子に塩化金酸塩、ロダンアンモン、
チオ硫酸ナトリウム及びチオ尿素系化合物を添加
し、化学熟成した。 この粒子70gあたりトメリチロールプロパン11
g及び安定剤、増粘剤を加え、その他に第1表に
示す化合物を含有せしめて、乳剤調製液を作成し
た。この乳剤調製液と下記に記す保護層液を、乳
剤液は銀量として4.8g/m2、保護層液はゼラチ
ン量として1.0g/m2となるように、コーテイン
グスピード150m/minでポリエチレンテレフタ
レート支持体上に同時塗布し、2分30秒で乾燥さ
しNo.1〜26の試料を得た。 〔保護層液〕 (イ) ●ゼラチン 100g ●C12H25−O−(CH2−CH2O)10−H 2.5g ● 2.0g ●ポリビニルピロリドン(平均分子量15000)
6g ●平均粒径2.5μのポリメチルアクリレート粒子
3g とシアヌルクロライド系硬膜剤と水を加えて
1.2に仕上げる。 (ロ) (イ)と同様の液に下記の化合物を添加したもの 0.5g/1.2保護層液 (ハ) (イ)と同様の液に下記の化合物を添加したもの
コロイダルシリカとしてルドツクスAM(デユ
ボン社製)を固形成分として全バインダーの
5wt%の相当分。 (ニ) (イ)と同様の液に(ロ)と(ハ)で添加した化合物を同
量添加したもの (ホ) (イ)と同様に液に下記の化合物を添加したもの 0.4g (ヘ) (イ)と同様の液に(ハ)と(ホ)で添加した化合物を同
量添加したもの 以上のようにして作成した試料は、塗布の1時
間後のものと、35℃80%RHの下で24時間調湿し
たものとを、それぞれ25℃20%RHの下で12時間
調湿し、同条件の下で帯電列が異なるネオプレン
ゴムロールとナイロンロールとで摩擦し、その後
自動現像機GX−300(小西六写真工業(株)製)と
XD−90(同社製)の現像液を用いて現像処理後、
発生スタチツクマークの度合いを判定した。その
結果は第1表に表した。評価は次のように行つ
た。 A:発生なし B:面積で3%未満発生 C: 〃 3%以上10%未満発生 D:面積で10%以上発生
Examples of the present invention will be described below. It should be noted that, as a matter of course, the present invention is not limited to the following examples. Example 1 2 mol% iodine and 0.2 mol% chlorine with an average particle size of 0.3μ
A silver iodobromide layer with a ratio of 40 mol% iodine and 60 mol% bromine was formed on the inner core of monodisperse silver chloroiobromide containing iodine and on the outside thereof, and the silver iodobromide layer was grown to a grain size of 0.5μ. A silver iodobromide layer was grown to a thickness of 0.85 μm at a ratio of 1 mol % bromine and 99 mol % to obtain slightly rounded tetradecahedral silver halide grains. These particles contain chloroaurate, rhodanammonium,
Sodium thiosulfate and thiourea compounds were added and chemically ripened. Tomelytylolpropane 11 per 70g of this particle
An emulsion preparation solution was prepared by adding g, a stabilizer, a thickener, and other compounds shown in Table 1. This emulsion preparation solution and the protective layer solution described below were coated with polyethylene terephthalate at a coating speed of 150 m/min so that the emulsion solution had a silver content of 4.8 g/m 2 and the protective layer solution had a gelatin content of 1.0 g/m 2 . They were simultaneously coated onto a support and dried for 2 minutes and 30 seconds to obtain samples Nos. 1 to 26. [Protective layer liquid] (a) ●Gelatin 100g ●C 12 H 25 −O−(CH 2 −CH 2 O) 10 −H 2.5g ● 2.0g ●Polyvinylpyrrolidone (average molecular weight 15000)
6g ●Polymethyl acrylate particles with average particle size of 2.5μ
Add 3g, cyanuric chloride hardener and water.
Finish it to 1.2. (b) The following compounds are added to the same liquid as in (a). 0.5g/1.2 protective layer solution (c) A solution similar to (a) with the following compounds added. Ludtux AM (manufactured by Dubon Co., Ltd.) is used as colloidal silica and the total binder is
Equivalent to 5wt%. (d) Same amount of the compounds added in (b) and (c) added to the same solution as in (a). (e) Same amount of the compounds added in (e) as in (a). 0.4g (F) The same amount of the compound added in (C) and (E) was added to the same solution as in (A). The humidity was conditioned for 24 hours at ℃ 80% RH, and the humidity was conditioned for 12 hours at 25℃ 20% RH under the same conditions, and rubbed between a neoprene rubber roll and a nylon roll with different charge series. After that, the automatic processor GX-300 (manufactured by Konishiroku Photo Industry Co., Ltd.)
After processing using XD-90 (manufactured by the same company) developer,
The degree of static mark occurrence was determined. The results are shown in Table 1. The evaluation was performed as follows. A: No occurrence B: Occurrence of less than 3% by area C: Occurrence of 3% or more but less than 10% D: Occurrence of 10% or more by area

〔保護層液〕[Protective layer liquid]

(ト) ●ゼラチン 100g ● 0.8g ● 0.5g ●平均粒径1.5μの二酸化ケイ素粒子 2g とビニルスルフオン系硬膜剤と水を加えて1.2
に仕上げる。 (チ) (ト)と同様の液に下記の化合物を固型成物とし
て全バインダーに対して4wt%相当物添加した
もの。 ●アルミナゾル AS−100(日産化学株式会社
製 粒径50〜100mμ×10mμ) (リ) ノニオンポリアルキレンオキシド化合物とし
て(チ)の液に下記の化合物を全バインダーに対し
て0.6wt%添加したもの。 これらの試料を実施例1と同一の試験と評価を
行ない、第2表にその結果を示した。
(g) ●Gelatin 100g ● 0.8g ● 0.5g ●Add 2g of silicon dioxide particles with an average particle size of 1.5μ, a vinyl sulfon hardener, and water to make 1.2
Finish it. (H) The following compound was added as a solid composition to the same liquid as in (G) in an amount equivalent to 4wt% based on the total binder. ●Alumina sol AS-100 (manufactured by Nissan Chemical Co., Ltd., particle size 50-100 mμ x 10 mμ) (1) As a nonionic polyalkylene oxide compound, the following compound was added to the solution in (1) at 0.6 wt% based on the total binder. These samples were subjected to the same tests and evaluations as in Example 1, and the results are shown in Table 2.

【表】【table】

〔発明の効果〕〔Effect of the invention〕

上述の如く、本発明のハロゲン化銀写真感光材
料は、さまざまな保存及び使用条件に対して良好
な帯電防止性能を示すことができるという効果を
有する。
As described above, the silver halide photographic material of the present invention has the effect of exhibiting good antistatic performance under various storage and usage conditions.

Claims (1)

【特許請求の範囲】 1 支持体上にハロゲン化銀乳剤を含有する層を
少なくとも1層有する写真構成層を有して成るハ
ロゲン化銀写真感光材料において、 該ハロゲン化銀乳剤層を有する側の写真構成層
の少なくともいずれかの層は、含フツ素界面活性
剤と、無機アルカリ金属塩と、平均粒径0.8μ以下
のポリマーラテツクスまたは平均粒径0.8μ以下の
無機コロイド物の少なくともいずれかである微粒
子とを含有し、 写真構成層の全バインダーに対し (a) 無機アルカリ金属塩は0.5〜5wt%であり、 (b) ポリマーラテツクスまたは無機コロイド物で
ある微粒子は3wt%以上である ことを特徴とするハロゲン化銀写真感光材料。
[Scope of Claims] 1. In a silver halide photographic light-sensitive material comprising a photographic constituent layer having at least one layer containing a silver halide emulsion on a support, the side containing the silver halide emulsion layer At least one of the photographic constituent layers contains a fluorine-containing surfactant, an inorganic alkali metal salt, a polymer latex with an average particle size of 0.8 μm or less, or an inorganic colloid with an average particle size of 0.8 μm or less. (a) The inorganic alkali metal salt is 0.5 to 5 wt%, and (b) The fine particles of polymer latex or inorganic colloid are 3 wt% or more based on the total binder of the photographic constituent layer. A silver halide photographic material characterized by:
JP22553385A 1985-10-09 1985-10-09 Silver halide photographic sensitive material Granted JPS6285240A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP22553385A JPS6285240A (en) 1985-10-09 1985-10-09 Silver halide photographic sensitive material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP22553385A JPS6285240A (en) 1985-10-09 1985-10-09 Silver halide photographic sensitive material

Publications (2)

Publication Number Publication Date
JPS6285240A JPS6285240A (en) 1987-04-18
JPH0564781B2 true JPH0564781B2 (en) 1993-09-16

Family

ID=16830786

Family Applications (1)

Application Number Title Priority Date Filing Date
JP22553385A Granted JPS6285240A (en) 1985-10-09 1985-10-09 Silver halide photographic sensitive material

Country Status (1)

Country Link
JP (1) JPS6285240A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01147449A (en) * 1987-12-03 1989-06-09 Konica Corp Silver halide photographic sensitive material for laser source

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5570837A (en) * 1978-11-24 1980-05-28 Konishiroku Photo Ind Co Ltd Silver halide photographic material
JPS56109336A (en) * 1980-02-01 1981-08-29 Konishiroku Photo Ind Co Ltd Silver halide photographic sensitive material
JPS59214849A (en) * 1983-05-21 1984-12-04 Mitsubishi Paper Mills Ltd Silver halide photographic material and its developing method

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5570837A (en) * 1978-11-24 1980-05-28 Konishiroku Photo Ind Co Ltd Silver halide photographic material
JPS56109336A (en) * 1980-02-01 1981-08-29 Konishiroku Photo Ind Co Ltd Silver halide photographic sensitive material
JPS59214849A (en) * 1983-05-21 1984-12-04 Mitsubishi Paper Mills Ltd Silver halide photographic material and its developing method

Also Published As

Publication number Publication date
JPS6285240A (en) 1987-04-18

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