JPS6114632A - Photosensitive material - Google Patents

Photosensitive material

Info

Publication number
JPS6114632A
JPS6114632A JP13588484A JP13588484A JPS6114632A JP S6114632 A JPS6114632 A JP S6114632A JP 13588484 A JP13588484 A JP 13588484A JP 13588484 A JP13588484 A JP 13588484A JP S6114632 A JPS6114632 A JP S6114632A
Authority
JP
Japan
Prior art keywords
layer
photosensitive material
present
photographic
monomer
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.)
Granted
Application number
JP13588484A
Other languages
Japanese (ja)
Other versions
JPH0411014B2 (en
Inventor
Toru Kobayashi
徹 小林
Koichi Nagayasu
浩一 永安
Norihata Tachibana
範幾 立花
Kosaku Masuda
功策 益田
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 JP13588484A priority Critical patent/JPS6114632A/en
Publication of JPS6114632A publication Critical patent/JPS6114632A/en
Publication of JPH0411014B2 publication Critical patent/JPH0411014B2/ja
Granted legal-status Critical Current

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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
    • G03C1/89Macromolecular substances therefor

Landscapes

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

Abstract

PURPOSE:To reduce electrostatic chargeability and to prevent the generation of static marks, especially, in a low humidity atmosphere by leaving specified F-contg. copolymer particles disclosed to the outermost layer of a photosensitive material. CONSTITUTION:The outermost layer on the photosensitive layer side of the photosensitive material or the backing layer of the support contains as a matting agent, fine particles in a size of 1-5mum dispersed into a binder, and made of a copolymer represented by formula I in which A is a monomer having >=2 ethylenically unsatd. double bond and B is a monomer having alpha,beta-ethylenically unsatd. double bonds and contg. F; x is 0.5-50mol%; y is 0-49.5mol%; and z is 50-99.5mol%: such as formula II. As a result, static marks due to charging in the manufacturing process of the photosensitive material and its handling, especially, even in a low humidity atmosphere, static electricity trouble can be prevented.

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、写真感光材料に関し1更1こ詳しくは特に低
温度雰囲気中における静電気特性が改良された’U *
感光材料に関する。 (従来技術) 一般に写真感光材料は、絶縁性のプラスチックフィルム
支持体上に同様に絶縁性の写真構成層、例えば感光性層
などが塗設されて構成されている。 従って写真感光材料を取り扱う場合には、例λば摩擦や
剥離などにより帯電し易く、塵埃の吸引、電撃、引火な
どの各種の現象を起して商品価値Iこ障害を与えること
が知られている。 その−例を挙げれば、ハロゲン化鋏写真感光材料は前記
のような絶縁性のプラスザックフィルム支持体上に感度
の高い写真感光性層が塗設されて製られており、その製
造工程、すなわち感光材料の巻き取り、巻き返し、ある
いは感光性層を始めとする各種の構成層の塗布、および
乾燥時における搬送工程中に感光材料の被膜層面が他の
物質との間で摩擦や剥離を受けて帝[L、放電に際して
感光材料が感光して、現像後、所謂スタチックマークと
呼ばれる不規則な静電気による感光むらを発生すること
がある。 才た写真感光材料は、その製造時ばかりでなく、画像を
得るために処理したりする際にも静電気が発生し、帯電
したり、肱埃を付着させたり、または前記のようなスタ
チックマークを発生させて故障の原因となる。 上記のスタチックマークは、写真感光材料の感度が高け
れば高いほど発生が著るしく、最近における写真感光材
料の高感度化に加えて、高速自動処理化による苛酷な機
械的取り扱いを受ける機会が多くなったことによって、
更に前記のような故障が多発する傾向にあると考えられ
る。 そこでこのような写真感光材料の帯電を防止する方法が
検討され、各種の改良手段が提案されている。例えば米
国特許第2,322,037号にはシリカ、スターチ、
ポリメチルメタクリレート、ポリビニルアセテート、ポ
リビニルアルコール、セルロースアセテート・プロピオ
ネート、エチルセルロースなどの粉末、所謂マット剤を
感光材料の表面層に用いて写真フィルムの帯電を防止し
た技術が記載されている。 才た与真感元刊料に用いられるマント剤としては、上記
のほかに、酸化チタン、硫酸バリウム、酸化マグネシウ
ム、炭酸亜鉛、炭酸カルシウム、ガラス球、タルクの如
き無機のマット剤も良く知られている。 そしてこれらマット剤の効果については、相接する写真
感光材料の他の表面と接触する面あるいは製造工程時の
搬送ロールの表面との接触面をできるだけ小さくして、
部相互間の接触分離により生ずる静電気の発生を小さく
することにあると考えられる。 しかしながら、従来公知のマット剤の殆A、どのものは
、それ自身では若干の帯電を低下せしめる傾向にはある
ものの、静電気の発生蓋からめると、それ程効果がある
とは言えず、更に最近における写真感光材料の高感度化
あるいは!!!造時の塗布速度の大幅アップおよび高速
自動処理化などによる苛酷な機械的取り扱いを受ける機
会の増大等の状況下では上記の如きマット剤の帯電防止
への寄与は非常jこ小さい。 また廟機マント剤としてポリメチルメタクリレートやポ
リスチレンのパール重合体等が広く用いられてはいるが
、これらの有機マント剤は有機溶媒中では膨潤または溶
解して使用することができなくなるという欠膚な有して
いる。 珪た一力、削iLシのマット剤の使用以外にも、例えば
吸湿性の物Mi才たは導電性の性質を用いて支持体表面
を処理し、あるいはハロゲン化釧写真感光材料の構成層
、特にその表面層中に上記の如き物質を含有させて、感
光材料に導電性を付与し、靜を気を蓄積し難くする方法
も知られている。 しかしながら、これらの殆んど多くは低湿度領域では気
運にその効果が失われ、満足し得る帯電防止性能を得る
ことは難かしく、尚、問題を残している。 (発明が解決りようとする問題点) そこで本発明は、写真感光材料の低湿度雰囲気下におけ
る静電気特性、特に静電気の発生を防止する方法を提供
することに係る。 才た本発明は第2に、有機溶媒中でも使用できるマット
剤を含有し、優れた静電気特性を有する写真感光材料を
提供することにある。 (問題点を解決するための手段) 本発明によれば下記一般式で示さおるフッ累a有共重合
体粒子が感光材料の最外層から露出して存在する写真感
光材料により上記課題を解決することができる。 一般式 %式%) 式中、Aは少くとも2個のエチレン性不飽和二重結合を
有するモノマー、Bはα、β−エチレン性不飽和二重結
合を有するモノマー、Cはα、β−エチレン性不飽和二
重結合を有するフッ素含有七ツマ−を表わし、Xは05
〜50モル%、Y i;It O〜49.5モル%、2
は50〜995モル%を表わす。 以下、本発明を更に詳細に駅間する。 先づ本発明に係る一般式で示されるフッ素含有共重合体
について詳述すれば、一般式で示される共重合体におけ
る単量体単位Aで表わされる単量体としては、例えばジ
ビニルベンゼン、アリルアクリレート、アリルメタクリ
レート、1,3−プチレンジアクリレート、1,3−ブ
チレンジメタクリレート、ジエチレングリコールジアク
リレート、ジエチレングリコールジメタクリレート、ビ
ニルアクリレート、ビニルメタクリレート、トリエチレ
ングリコールジアクリレート、トリエチレングリフール
ジメタクリレート、エチレンジアクリレート、エチレン
ジメタクリレート、1.6−ヘキサンジアクリレート、
1.6−ヘキサンジメタクリレート尋を挙げることがで
きる。 才た単量体単位Bで表わされる単量体としては、例えば
エチレン、プロピレン、1−ブテン、イソブチン、2−
メチルベンゼン、2−メチルブテン、1.1,4.4−
テトラメチルブタジェン、スチレン、α−メチルスチレ
ン、酢酸ビニル、酢酸アリル、メチルメタクリレート、
エチルアクリレート等を挙げることができる。これらB
で表わされる単量体の中でメチルメタクリレートおよび
スチレンが硬度の点で奸才しい。 次1ζCで表わされる単量体としては、例えば上記の化
合物を挙げることかできる。 fl)   CO3−CIIF      f2)  
 CO3−CF’2f31   CHF = CP2f
4)   CF″2= CF2Qo)  CO3−C(
CH3) −C00CH2CF3(Ill  C1−1
2= C(CH3)−C00CH2C2F。 (12)   CO3−CH C00CH2(CF2)rIH(n = 2〜9 )Q
3)   Cl42= C−CHs C00CH2(CF2 )。II      (n =
 2〜9  )(141C112= C−e113 C00CII2CH20(CF2 )。F  (。工2
〜8)0η  CO3−C1 C00C112C112(CF2)nF    (n 
= 2〜8 )111elf。=C1( ■ C00CI(2CI(CH2(C1!’2 )nF  
 (n = 2〜8 )〇II (19)   C112= C−(’II3C00(’
ll−CF211CF3 C211゜ C00C−CF2CFHCF3 「 さらに前記一般式においてx、y、tが表わすモル比に
ついては、マット剤自身が溶媒に不溶であるため1こは
、Xは05以上であることが必要であり、才た静電気特
性を良くするためには2を50以上にすることが必要で
ある。 下記に一般式で表わされる本発明1こ係るフッ素含有共
重合体の代表的具体例を記載する。 い・とン (1)                C1−13+
CHCH2+ (x  :  y  :  z=lO:30:6(1)
(2)                      
CH3t31                   
 C113(x  :  z  〜40 : 6(1)
I C0O(’112 +C112−C11+ (x  : y  :  z =10:10 :80)
(−C1l −CI!2 + (x  :  y  :  z= 5:25ニア0)本
発明は、上記に例小された如きフッ素含壱共重イタ体に
のみ限Wされるものではない。本発明によれば本発明に
係ろ°ツノ素含有共重合体粒子は以−トのよ51こして
製】i’t−rることができるO製造例1 2%ゼラチン水溶液200m7中に炭酸カルシウム12
yを加え、ホモジナイ→ターで20分間分散する。 次いでこの中にジビニルベンセフ13g1ヘキ→夛70
ロイソプロヒル了クリレート13.3.SJ、メチルメ
タクリレ−1−3,09およびヘンソイルパーオキンド
0.5.9を加え、窒素気流中80〜85°Cで15分
間1000回転/分の速度で攪拌りながら重合させた。 得られたエマルジョンを光学顕微鏡で観察した結果、2
〜5μのポリマー油滴が認めら才lた。この−1フルジ
ーンを遠心分離にかけ、粒子+1イス゛2〜57+のマ
ット剤を得た。収率96%、元木分析結米から目的の例
7層共重合体化合物(1)であると、とを確認シた0 次に本発明の写真感光材料について述べれば、本発明で
言う写真感光材料とは、写真感光材料に用いられる支持
体ならびにこの支持体(必要に応じて下引加工を施した
もの、あるいはバッキング層を塗設したもの等を含む)
上に、1層または2層以上の写真構成層る塗設した中間
製品としての写真感光材料および上記支持体上にハロゲ
ン化釧乳剤層、下引層、中間層、フィルタ一層、ハレー
ション防止層、保護層、バッキング層等の写真構成層を
塗設し、た完成製品としての写真感光材料等すべてのも
のを含むものである。 従って本発明において、本発明に係るフッ素含イ1共重
合体粒子(本発明に係るマット剤と呼ぶ)を写真感光材
料の最外層に存在させるというこきは、上記の中間層d
)1ならひに完成製品としての写真感光材料の最外表面
に本発明に係るマット剤を介イtさ1上ろことを意味し
、本発明においては、例X、げ′/7貞感光感光材料持
体の表面もしくは背面に直接または下引層を介してマン
ト剤を存在させる場イヤ、写真感光材料の構成層の1つ
才たは2つ以」−の層を塗設した中間製品の最外層1こ
存在させる場合、ならびに最終製品である写真感光材料
の感光層が塗設されている側の最外層、または支持体を
はさんで上記感光層とは反対側のバッキング層の最外層
に介在させる場合等が含才れる。 本発明に係るマント剤を写真感光材料の最外層にrf在
せしめるには、例えば写Jlc構成層のバインターであ
るセラチンの如き親水性コロイドと混合し、通常の塗布
手段により塗布し、乾燥すればよい。その他の手段とし
ては、写真感光相打構成層の最外層に本発明に係るマッ
ト剤を混合するか、抜たは構成層とマント剤とをそれぞ
れ別個に噴霧ないしはスーパーml −1−した後に乾
燥1れば良い。 本発明に係るマノ]・剤の粒径は01μ〜10μ、好ま
しくは1μ〜5μであるが、本発明の効果な♂くわすに
は、少くともマット剤杓子が構成層から露出することが
必要なので、バインダーと混イj L −(いる場合に
は、その乾燥膜厚より大きいことがbfまLい。 尚、粒子が層から露出するとは、層にある稈1ηの表1
1廿1さを与ス、之)ことであって、必ずしもh−fそ
の0σ)がb\出しでいる必要はない。 また上記マット剤の塗布には、マット効果を向上させる
目的では多い程効果的であるが、透明例または鮮鋭性に
悪影響を及ぼさない程度の孕布脩であることが好ましく
、一般的には10〜50owy/m′、さらに奸才しく
け50〜200 *9 / m’の範囲である0 本発明に係るマット剤は、他のマット剤と混合して使用
することもできるが、効果の点から本発明に係るーlマ
ット剤り少曹用いることが好7+−い。 次1c本発明の写真感光材料にj、iいて使用されイ。 支持体と(−て1f1例才ば三酢酸(ζルl]−スーノ
イルム、ポリ、[チL/ンラL・フタレートフィII)
、などの1;り王−4チル°ノイルム、ポリカーボネー
トフィル11、ポリスチレンフィルム、ポリオレフィン
フィルノ8、ポリエチレン′ノミネート紙などのよりな
釣(ミ水性フィルムまたはシート等が含まれる。 本発明の写真感光(イ料としては、ハロケン化釧写爽感
光材料が6f IF l、く、一般白黒用感光材料、特
殊白黒用感光((杓、勾う−用感光材料、印刷用感電材
料、X線用感電4(料再種々のものの中間製品および完
成品が挙けζ)れる。 本発明の写iLA・に尤+・1料がハロゲン化鋏写真感
光材料である場イ1に用いろハロゲン化銀乳剤には臭化
銀、塩化銀、塩臭化銀、沃臭化銀、塩沃臭化釦等の梱々
のハロケン化釧粒子が親水性高分子バインター中に分散
されたものが用いられ、Jたバインダーとしては、例え
ばセラチン、セラチン訪導体、−」ロイド状アルブミン
、寒天、アうヒアゴノ1、アルキン酸、例んばアセチル
含有1i19〜26%にまで加水J) Mされたセル[
コーズアセテートの如きセルローズ誘導体、アクリルア
ミド、イミド化ポリアクリルアミド、カセイン、例えば
ビニルアル−7−ル、ビニルシアノアセテートコポリマ
ーの如きウレタンカルボン酸蓋Jたはシアノアセチル蓋
を含むビニルアルコールポリマー、ポリビニルアルコー
ル、ポリビニルピロリドン、加水分解ポリビニルアセテ
ート、蛋白質才たは飽和アンル化蛋白貿とビニル蓋を有
する七ツマ−との重合で得られるポリマー等を用いるこ
とができる。そして)・ロゲン化銀乳剤は化学増感剤、
例えばア11ルーyAカルバミド、チオ尿素、アリルイ
ンチオシアオート、チオ硫酸ナトリウム、シスチン等の
硫黄増感剤、活性あるいは不活性のセレン増感剤、例え
ばカリウムクロロオーシート、オーリックトリク
(Industrial Application Field) The present invention relates to a photographic material, and more particularly, the present invention relates to a photographic material having improved electrostatic properties particularly in a low-temperature atmosphere.
Regarding photosensitive materials. (Prior Art) Generally, a photographic light-sensitive material is constructed by coating a similarly insulating photographic constituent layer, such as a photosensitive layer, on an insulating plastic film support. Therefore, when handling photographic materials, it is known that they are easily charged due to friction or peeling, and can cause various phenomena such as dust attraction, electric shock, and ignition, which can damage the product value. There is. For example, a halogenated scissor photographic light-sensitive material is manufactured by coating a highly sensitive photographic layer on an insulating plastic film support as described above, and the manufacturing process, namely During the winding and rewinding of the photosensitive material, the application of various constituent layers including the photosensitive layer, and the transportation process during drying, the surface of the coating layer of the photosensitive material may be subjected to friction or peeling from other substances. The photosensitive material is exposed to light during discharge, and after development, uneven exposure due to irregular static electricity called so-called static marks may occur. Static electricity is generated in advanced photographic materials not only during manufacture, but also during processing to obtain images, which can lead to static electricity, buildup of dust, and the formation of static marks as described above. This may cause a malfunction. The above-mentioned static marks are more likely to occur as the sensitivity of the photographic light-sensitive material increases, and in addition to the recent increase in the sensitivity of photographic light-sensitive materials, the opportunity for them to be subjected to harsh mechanical handling due to high-speed automatic processing has increased. Due to the increase in
Furthermore, it is thought that the above-mentioned failures tend to occur frequently. Therefore, methods of preventing such charging of photographic light-sensitive materials have been studied, and various improvement measures have been proposed. For example, U.S. Patent No. 2,322,037 describes silica, starch,
A technique is described in which a so-called matting agent, a powder of polymethyl methacrylate, polyvinyl acetate, polyvinyl alcohol, cellulose acetate propionate, ethyl cellulose, etc., is used in the surface layer of a photosensitive material to prevent charging of a photographic film. In addition to the above, inorganic matting agents such as titanium oxide, barium sulfate, magnesium oxide, zinc carbonate, calcium carbonate, glass bulbs, and talc are also well known as capping agents used in Saita Yoshinkan Genkansho. ing. The effects of these matting agents can be achieved by minimizing the surface that contacts other surfaces of the adjacent photographic material or the surface of the conveyor roll during the manufacturing process.
This is thought to be aimed at reducing the generation of static electricity caused by contact separation between parts. However, although most of the conventionally known matting agents tend to reduce static electricity by themselves, they cannot be said to be very effective when viewed from the lid that generates static electricity. Increasing the sensitivity of photosensitive materials or! ! ! Under conditions such as a significant increase in coating speed during manufacturing and increased opportunities for severe mechanical handling due to high-speed automatic processing, the contribution of the above-mentioned matting agent to antistatic properties is very small. Furthermore, although polymethyl methacrylate and polystyrene pearl polymers are widely used as mausoleum mantle agents, these organic mantle agents swell or dissolve in organic solvents, making them unusable. have. In addition to using a matting agent, for example, the surface of the support may be treated with a hygroscopic material or a conductive material, or the constituent layers of a halogenated photographic light-sensitive material may be treated. In particular, a method is known in which the above-mentioned substances are contained in the surface layer of the photosensitive material to impart electrical conductivity to the photosensitive material and thereby make it difficult for the photosensitive material to accumulate moisture. However, most of these lose their effectiveness in low humidity areas, making it difficult to obtain satisfactory antistatic performance, and problems still remain. (Problems to be Solved by the Invention) Therefore, the present invention relates to providing a method for preventing the electrostatic properties of a photographic light-sensitive material in a low-humidity atmosphere, particularly for preventing the generation of static electricity. A second object of the present invention is to provide a photographic material containing a matting agent that can be used even in an organic solvent and having excellent electrostatic properties. (Means for Solving the Problems) According to the present invention, the above-mentioned problems are solved by a photographic light-sensitive material in which fluorine-containing copolymer particles represented by the following general formula are exposed from the outermost layer of the light-sensitive material. be able to. General formula % Formula %) In the formula, A is a monomer having at least two ethylenically unsaturated double bonds, B is a monomer having α, β-ethylenically unsaturated double bonds, and C is α, β- Represents a fluorine-containing septamer having an ethylenically unsaturated double bond, where X is 05
˜50 mol%, Y i ; It O ˜49.5 mol%, 2
represents 50 to 995 mol%. The present invention will be explained in more detail below. First, to explain in detail the fluorine-containing copolymer represented by the general formula according to the present invention, examples of the monomer represented by the monomer unit A in the copolymer represented by the general formula include divinylbenzene, allyl, Acrylate, allyl methacrylate, 1,3-butylene diacrylate, 1,3-butylene dimethacrylate, diethylene glycol diacrylate, diethylene glycol dimethacrylate, vinyl acrylate, vinyl methacrylate, triethylene glycol diacrylate, triethylene glycol dimethacrylate, ethylene dimethacrylate Acrylate, ethylene dimethacrylate, 1,6-hexane diacrylate,
Mention may be made of 1,6-hexane dimethacrylate. Examples of the monomer represented by the monomer unit B include ethylene, propylene, 1-butene, isobutyne, 2-
Methylbenzene, 2-methylbutene, 1.1,4.4-
Tetramethylbutadiene, styrene, α-methylstyrene, vinyl acetate, allyl acetate, methyl methacrylate,
Examples include ethyl acrylate. These B
Among the monomers represented by , methyl methacrylate and styrene are outstanding in terms of hardness. Examples of the monomer represented by 1ζC include the above-mentioned compounds. fl) CO3-CIIF f2)
CO3-CF'2f31 CHF = CP2f
4) CF″2= CF2Qo) CO3-C(
CH3) -C00CH2CF3(Ill C1-1
2=C(CH3)-C00CH2C2F. (12) CO3-CH C00CH2 (CF2) rIH (n = 2-9) Q
3) Cl42=C-CHs C00CH2 (CF2). II (n =
2-9) (141C112=C-e113 C00CII2CH20(CF2).F (.Eng.2
~8) 0η CO3-C1 C00C112C112(CF2)nF (n
= 2~8) 111elf. =C1( ■ C00CI(2CI(CH2(C1!'2)nF
(n = 2~8)〇II (19) C112=C-('II3C00('
ll-CF211CF3 C211゜C00C-CF2CFHCF3 "Furthermore, regarding the molar ratio represented by x, y, and t in the above general formula, since the matting agent itself is insoluble in the solvent, X must be 05 or more. Therefore, in order to improve the excellent electrostatic properties, it is necessary to set 2 to 50 or more.Representative examples of the fluorine-containing copolymer according to the present invention 1 represented by the general formula are described below. Iton (1) C1-13+
CHCH2+ (x:y:z=lO:30:6(1)
(2)
CH3t31
C113(x:z~40:6(1)
I C0O('112 +C112-C11+ (x:y:z=10:10:80)
(-C1l-CI!2+(x:y:z=5:25near 0) The present invention is not limited to the fluorine-containing 1-copolymer ita-isomer as mentioned above. According to the present invention, the copolymer particles containing silane can be prepared as follows: Preparation Example 1 Calcium carbonate in 200 m7 of a 2% gelatin aqueous solution 12
Add y and disperse with a homogenizer for 20 minutes. Next, add 13 g of divinylbencef to this → 70
Leisoprohil acrylate 13.3. SJ, methyl methacrylate-1-3,09 and Hensoylperoquind 0.5.9 were added and polymerized at 80-85°C in a nitrogen stream for 15 minutes with stirring at a speed of 1000 revolutions/minute. As a result of observing the obtained emulsion with an optical microscope, 2
~5μ polymer oil droplets were observed. This -1 full gene was centrifuged to obtain a matting agent of particles +1 size 2 to 57+. The yield was 96%, and Motoki analysis confirmed that it was the desired Example 7-layer copolymer compound (1). A photosensitive material refers to a support used in a photographic photosensitive material, and this support (including those that have been subjected to undercoating processing or coated with a backing layer, etc., if necessary).
A photographic light-sensitive material as a coated intermediate product having one or more photographic constituent layers thereon, and a halogenated emulsion layer, a subbing layer, an intermediate layer, a filter layer, an antihalation layer, It includes all photographic light-sensitive materials as finished products coated with photographic constituent layers such as protective layers and backing layers. Therefore, in the present invention, the fact that the fluorine-containing 1-copolymer particles according to the present invention (referred to as the matting agent according to the present invention) are present in the outermost layer of the photographic light-sensitive material is based on the above-mentioned intermediate layer d.
) 1 means that the matting agent according to the present invention is applied to the outermost surface of the photographic light-sensitive material as a finished product. An intermediate product coated with one or more of the constituent layers of the photographic light-sensitive material, in which a mantle agent is present on the surface or back of the light-sensitive material support directly or via a subbing layer. The outermost layer of the photographic material as the final product is the outermost layer on the side on which the photosensitive layer is coated, or the outermost layer of the backing layer on the opposite side of the support from the photosensitive layer. This includes the case where it is interposed in the outer layer. In order to make the mantle agent according to the present invention RF present in the outermost layer of a photographic light-sensitive material, for example, it is mixed with a hydrophilic colloid such as seratin, which is a binder of the photographic JLC constituent layer, coated by a conventional coating method, and dried. good. Other means include mixing the matting agent according to the present invention into the outermost layer of the photographic photosensitive layer and the capping agent, or spraying the component layer and the capping agent separately or drying after drying. 1 is enough. The particle size of the matting agent according to the present invention is 01μ to 10μ, preferably 1μ to 5μ, but in order to achieve the effect of the present invention, it is necessary that at least the matting agent ladle is exposed from the constituent layer. Therefore, if the binder is mixed with the binder, it must be larger than the dry film thickness.In addition, when particles are exposed from the layer, Table 1 of the culm 1η in the layer is used.
It is not necessary that h−f(0σ) be b\out. In addition, when applying the above-mentioned matting agent, the more the matting agent is applied, the more effective it is for the purpose of improving the matting effect, but it is preferable to apply the matting agent to a degree that does not adversely affect transparency or sharpness, and generally 10 ~50owy/m', and furthermore, the matting agent according to the present invention can be used in combination with other matting agents, but the effectiveness Therefore, it is preferable to use the matting agent according to the present invention. The following 1c are used in the photographic material of the present invention. With a support (-te1f1 example: triacetic acid (ζrul)-sunoyl, poly, [thiL/nra-L phthalate fi II)
, etc. 1; Polycarbonate film 11, polystyrene film, polyolefin Filno 8, polyethylene' nominated paper, etc. (includes water-based films or sheets, etc.). (As a material, halogenated photosensitive material is 6F IF l, general photosensitive material for black and white, photosensitive material for special black and white (photosensitive material for ladle, dip, electric shock material for printing, electric shock for X-ray) 4 (including intermediate products and finished products of various materials). Silver halide emulsion used in 1 when the material is a halogenated photographic light-sensitive material. In J. Examples of the binder include seratin, seratin conductor, -loid albumin, agar, acetate, alkinoic acid, and acetyl-containing binder hydrated to a concentration of 19 to 26%.
Cellulose derivatives such as cause acetate, acrylamide, imidized polyacrylamide, casein, vinyl alcohol polymers containing urethane carboxylic acid caps or cyanoacetyl caps such as vinylal-7-al, vinylcyanoacetate copolymers, polyvinyl alcohol, polyvinylpyrrolidone Polyvinyl acetate, hydrolyzed polyvinyl acetate, a polymer obtained by polymerizing a proteinaceous compound or a saturated unsaturated proteinaceous compound with a vinyl capped hexamer, etc. can be used. And)・Silver halide emulsion is a chemical sensitizer,
For example, sulfur sensitizers such as A11-YA carbamide, thiourea, allyl inthiocyate, sodium thiosulfate, cystine, active or inactive selenium sensitizers, such as potassium chloroosete, auric trichloride, etc.

【−】
ライド、カリウムオーリツクチオシγl−ト、2−オー
ロチアベンゾチアゾールメチルクロライド等の金化合物
、例えばアンモニウムクロ
[-]
gold compounds, such as ammonium chloride, potassium auryl thiol, 2-aurothiabenzothiazole methyl chloride, etc.

【コパファート、ナトリつム
クロロバラダイト等のバランτ”ツム化合物、例えばカ
リウムクロロブラゴイート等のプラナニウム化合物、お
よびルテニウム化合物、ロジウム化合物、イリジウム化
什物等の黄金属増感剤Jたはこのような増感剤の組合せ
を用L1て増感することができる。またこの乳剤は化学
増感以外にも還元剤で還元増感することができト11ア
ゾール類、イミダソール類、アサインデン類、ベンゾチ
アゾリウム化合物、亜鉛化合物、カドミウム化合物、メ
ルカプタン類またはこれらの混合物で安定化することが
でき、またチオエーテル類、第4級アンモニウム塩類ま
たはポリアルキレンオキ廿イド類の増感化合物を含有せ
しめることができる。そしてまたこの乳剤は、例えばグ
リセリン、1.5−ベンタンジオール等のヒト0キシア
ルカン、エチレンビスグリコール酸のエステル、ヒ゛ス
エトキシジエチレングリコールサクシネート、乳化重合
によって得られる水分散性の微粒子状高分子化合物等の
湿潤剤、あるいは可塑剤、膜物性改良剤等を含有せしめ
ることができ、さら1こエチレンイミン系化合物、ビニ
ルスルホン糸化合物、ジオキサン誘導体、オキシポリサ
ッカライド、ジカルボン酸クロライド、メタンスルホン
酸のヒ゛ニスチル等の硬膜剤、→トボアン、スルホニ】
ノ1り酸塩4りの塗布助剤、螢光増白剤、界面活性剤、
γンf−:1テイン剤等の撞々の写真用添加剤を含有せ
l b’)イ+ことができる。 さらにこのハロゲン化銀乳剤は、/アニン色素、メロシ
アニン色素、収金シアニン色素、←γ、  、   ・
−一・ −く等を用いて坑学j11g感されてもよい。 才た無色カプラー、カラードカプラー、現像抑制剤放出
カプラー等の徨々σ)カプラーを含不してもよい。ノ・
ロゲン化銀乳へり層以外J)層中にも前1i己の如き種
々の写真用添加剤を含有1トしぬることができ、そのバ
インダーとしてらINI 記と同様のものを使用するこ
とができる。本発明に係るマット剤を本発明に従って写
真感光材料の′lJ真構成層の最外層に露出して介在せ
しめることにより、スタチックマーク故障等の帯電故障
のな0感光材料を得ることができる。しかも本発明によ
れば、上記のマント剤の使用により感光材料の感光度、
階調性、カプリ等の写真特性には側らの悲影#を及ぼす
ことはない〇 =18− 以下、本発明を実施例により更に具体的に記載するが、
本発明はこれにより限定されるものではない。 実施例1 乳剤1 kg当り35gのゼラチンと100 IIの沃
臭化銀(3モル%の沃化銀を含む)とを含崩する沃臭化
銀ゼラチン高感度X線用乳剤に対して第2熟成時1こ金
増感および硫黄増感を行った後、安定剤として、4−ヒ
ドロキシ−6−メチル−1,3,3a。 7−チトラザインデン化合物、硬膜剤としてグリオキザ
ール、塗布助剤としてサポニンを加え、下引処理を施し
た厚さ175μのポリエチレンテレフタレートフィルム
支持体上に乾燥膜厚が7μになるように塗布乾燥し、次
いで下記組成の保護層を乾燥膜厚が約1μmこなるよう
に塗布乾燥し、試料−1を得た。 (保護層組成) (9/ln″) ゼラチン               10gシー2
−エチルへキシルスルホコハク酸ナトリウム     
            0.01.jZグリオキザー
ル           0.01.!i+上記の保護
層組成物に前記製造例1により得られた本発明に係るマ
ット剤(例示共重合体化合物(1)の粒子)を50 Q
 / y(’の割合になるように添加し、得られた試料
を試料−2とした。 一方、比較用として平均粒径3μのPMMAを同様1こ
50 ml? / m”になるように前記保護層組成物
に添加して得られた試料を試料−3とする。 次に各試料について23℃、20%rtn W囲気中で
4時間調湿し、ネオプレンゴムによる摩擦帯電量の測定
およびスタチックマークの発生試験を行い、下記第1表
に示す如き結果を得た。 尚、上記の帯[誕は、ネオブレンゴムと試料間の摩擦帯
電にで、23°0.20%几11雰囲気中で測定したも
のであり、またスタチックマークは、23°Cl2O%
RI−T雰囲気中に4時間試料な調湿後、ネオブレンゴ
ム棒でこすり、現像した後、その黒化の度合をみて、下
記のグレードにより判定した。 グレード1:発生なし グレード2:僅かに発生 3゛発 生 4:やや多発 5:全面に発生 一上記の表が示すように、保護層にマット剤を全く添加
しなかった試料1および比較用のマット剤を含有させた
試料3は何れも正に大きく帯電し、かつスタチックマー
クの発生も強かった。しかしながら本発明に係るマント
剤を添加せしめた試料2では帯電量も小さく、かつスタ
チックマークの発生も殆んど認められなかった。 実施例2 三酢酸セルロースフィルム支持体のを面に下記の組成液
を約20xl/m′の割合でロール:j−ティング法で
塗布し、9(1’(Jで3分間乾燥し、さらに上記支持
体の表面1こ常法により下引処理した後、実施例1で作
製した試料−1と同じ高感度X線用乳剤および保護層を
順に塗布、乾燥り、試料−4を得た0 (組成液) セルロースジアセテート20g メタノール          700m1アセトン 
          300m、/一方、上記の組成液
に本発明に係るマット剤(例示共重合体(1+の粒子)
を6011i’ / yj添加したほかは、上記の試料
−4と同様にして作製された試料を試料−5とする。 上記により得られた各試料を実施例】と同様に処理し、
得られた結果を下記第2表に示す。 第  2  表 上記が示すように、本発明に係るマット剤を支持体のを
面塗布層に添加せしめた試料−5は、帯電量も少く、か
つスタチックマークの発生も殆んど認められなかった。 なお比較用試料−4には、ポリメチルメタクリレートお
よびポリスチレン等のマット剤を添加したが、液中で膨
潤、溶解が生起し、使用に耐えなかった。 (発明の効果) 本発明に係るフッ素含有共東合体粒子を感光材料の最外
層から露出して存在せしめた本発明の写真感光材料は、
特に低湿度雰囲気下において帯電量が小さく、かつスタ
チックマークの発生は殆んど誌められない。
[Balanium compounds such as copafate, sodium chlorovaladite, plananium compounds such as potassium chlorobragoate, and yellow metal sensitizers such as ruthenium compounds, rhodium compounds, iridium compounds, etc. The emulsion can be sensitized by using a combination of sensitizers.In addition to chemical sensitization, this emulsion can also be reduced sensitized with a reducing agent. It can be stabilized with zolium compounds, zinc compounds, cadmium compounds, mercaptans or mixtures thereof, and can contain sensitizing compounds such as thioethers, quaternary ammonium salts or polyalkylene oxides. This emulsion may also contain, for example, glycerin, human oxyalkanes such as 1,5-bentanediol, esters of ethylene bisglycolic acid, diethylene glycol succinate, water-dispersible fine particulate polymer compounds obtained by emulsion polymerization, etc. It can contain wetting agents, plasticizers, membrane property improvers, etc. In addition, ethyleneimine compounds, vinyl sulfone thread compounds, dioxane derivatives, oxypolysaccharides, dicarboxylic acid chlorides, vinistyl methanesulfonic acid, etc. hardening agent, → Toboane, sulfony]
Coating aids for monophosphate, fluorescent brighteners, surfactants,
[gamma]nf-:1 b') It is possible to contain various photographic additives such as staining agents. Furthermore, this silver halide emulsion contains /anine dye, merocyanine dye, cyanine dye, ←γ, , ・
- You may also feel the mineralogy j11g using -1, - etc. Coupler(s) such as colorless couplers, colored couplers, development inhibitor releasing couplers, etc. may not be included. of·
Various photographic additives such as those mentioned above can be incorporated in layers other than the silver halide milk edge layer, and the same binders as those mentioned above can be used. . By exposing and intervening the matting agent according to the present invention in the outermost layer of the true constituent layer of a photographic light-sensitive material according to the present invention, it is possible to obtain a zero-sensitive material free from charging failures such as static mark failures. Moreover, according to the present invention, the sensitivity of the photosensitive material can be improved by using the above-mentioned capping agent.
The present invention will be described in more detail with reference to Examples below.
The present invention is not limited thereby. Example 1 A second silver iodobromide gelatin high-sensitivity After performing gold sensitization and sulfur sensitization during ripening, 4-hydroxy-6-methyl-1,3,3a was used as a stabilizer. A 7-chitrazaindene compound, glyoxal as a hardening agent, and saponin as a coating aid were added, and the mixture was coated onto a polyethylene terephthalate film support with a thickness of 175 μm that had been subbed treated so that the dry film thickness was 7 μm, and then dried. A protective layer having the following composition was coated and dried to a dry film thickness of about 1 μm to obtain Sample-1. (Protective layer composition) (9/ln'') Gelatin 10g Sea 2
- Sodium ethylhexyl sulfosuccinate
0.01. jZ Glyoxal 0.01. ! i+ 50 Q
/y('), and the resulting sample was designated as sample-2. On the other hand, for comparison, PMMA with an average particle size of 3μ was added in the same manner as described above so that the amount was 50ml/m". The sample obtained by adding it to the protective layer composition is referred to as Sample-3.Next, each sample was conditioned for 4 hours at 23°C in a 20% rtn W atmosphere, and the amount of triboelectric charge was measured using neoprene rubber. A tick mark generation test was carried out, and the results were obtained as shown in Table 1 below.The above band [originated] due to the frictional electrification between the neorene rubber and the sample. The static mark is 23°Cl2O%
After conditioning the humidity of the sample in an RI-T atmosphere for 4 hours, rubbing it with a neorene rubber rod and developing it, the degree of blackening was observed and judged according to the following grade. Grade 1: No occurrence Grade 2: Slight occurrence 3゛ Occurrence 4: Slightly frequent occurrence 5: Occurrence all over the surface - As shown in the table above, Sample 1 in which no matting agent was added to the protective layer and Comparative All samples 3 containing a matting agent were positively charged to a large extent, and static marks were also strongly generated. However, in sample 2 to which the capping agent according to the present invention was added, the amount of charge was small and almost no static marks were observed. Example 2 The following composition solution was applied to the side of a cellulose triacetate film support at a rate of about 20xl/m' using a roll/j-ting method, dried for 3 minutes with a 9 (1') J, and then After surface 1 of the support was undercoated by a conventional method, the same high-sensitivity X-ray emulsion and protective layer as Sample-1 prepared in Example 1 were coated in order and dried to obtain Sample-4. Composition liquid) Cellulose diacetate 20g Methanol 700ml Acetone
300m/Meanwhile, a matting agent according to the present invention (exemplary copolymer (1+ particles)) is added to the above composition liquid.
Sample-5 is a sample prepared in the same manner as Sample-4 above, except that 6011i'/yj of 6011i'/yj was added. Each sample obtained above was treated in the same manner as in Example],
The results obtained are shown in Table 2 below. As shown in Table 2 above, Sample-5, in which the matting agent of the present invention was added to the surface coating layer of the support, had a small amount of charge and almost no static marks were observed. Ta. Although a matting agent such as polymethyl methacrylate and polystyrene was added to Comparative Sample 4, it swelled and dissolved in the liquid, making it unusable. (Effects of the Invention) The photographic light-sensitive material of the present invention, in which the fluorine-containing Kyodo polymer particles according to the present invention are exposed from the outermost layer of the light-sensitive material, has the following features:
Particularly in a low humidity atmosphere, the amount of charge is small, and static marks are hardly observed.

Claims (1)

【特許請求の範囲】 下記一般式で示されるフッ素含有共重合体粒子が感光材
料の最外層から露出して存在することを特徴とする写真
感光材料。 一般式 −(A)_x−(B)_y−(C)_z− 〔式中、Aは少くとも2個のエチレン性不飽和二重結合
を有するモノマー、Bはα,β−エチレン性不飽和二重
結合を有するモノマー、Cはα,β−エチレン性不飽和
二重結合を有するフッ素含有モノマーを表わし、xは0
.5〜50モル%、yは0〜49.5モル%、zは50
〜99.5モル%を表わす。〕
[Scope of Claims] A photographic light-sensitive material characterized in that fluorine-containing copolymer particles represented by the following general formula are exposed from the outermost layer of the light-sensitive material. General formula -(A)_x-(B)_y-(C)_z- [wherein A is a monomer having at least two ethylenically unsaturated double bonds, B is α,β-ethylenically unsaturated A monomer having a double bond, C represents a fluorine-containing monomer having an α,β-ethylenically unsaturated double bond, and x is 0
.. 5 to 50 mol%, y is 0 to 49.5 mol%, z is 50
It represents ~99.5 mol%. ]
JP13588484A 1984-06-29 1984-06-29 Photosensitive material Granted JPS6114632A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13588484A JPS6114632A (en) 1984-06-29 1984-06-29 Photosensitive material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13588484A JPS6114632A (en) 1984-06-29 1984-06-29 Photosensitive material

Publications (2)

Publication Number Publication Date
JPS6114632A true JPS6114632A (en) 1986-01-22
JPH0411014B2 JPH0411014B2 (en) 1992-02-27

Family

ID=15162033

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13588484A Granted JPS6114632A (en) 1984-06-29 1984-06-29 Photosensitive material

Country Status (1)

Country Link
JP (1) JPS6114632A (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5494319A (en) * 1978-01-09 1979-07-26 Konishiroku Photo Ind Co Ltd Silver halide photographic material
JPS5678834A (en) * 1979-12-03 1981-06-29 Fuji Photo Film Co Ltd Photographic sensitive material
JPS5711342A (en) * 1980-06-25 1982-01-21 Fuji Photo Film Co Ltd Photographic sensitive material

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5494319A (en) * 1978-01-09 1979-07-26 Konishiroku Photo Ind Co Ltd Silver halide photographic material
JPS5678834A (en) * 1979-12-03 1981-06-29 Fuji Photo Film Co Ltd Photographic sensitive material
JPS5711342A (en) * 1980-06-25 1982-01-21 Fuji Photo Film Co Ltd Photographic sensitive material

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Publication number Publication date
JPH0411014B2 (en) 1992-02-27

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