JPH052218B2 - - Google Patents

Info

Publication number
JPH052218B2
JPH052218B2 JP60265897A JP26589785A JPH052218B2 JP H052218 B2 JPH052218 B2 JP H052218B2 JP 60265897 A JP60265897 A JP 60265897A JP 26589785 A JP26589785 A JP 26589785A JP H052218 B2 JPH052218 B2 JP H052218B2
Authority
JP
Japan
Prior art keywords
resins
photographic
resin
surface layer
layer
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
JP60265897A
Other languages
Japanese (ja)
Other versions
JPS62125347A (en
Inventor
Kunyuki Goto
Keiji Yamaguchi
Masahiko Taguchi
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 JP26589785A priority Critical patent/JPS62125347A/en
Publication of JPS62125347A publication Critical patent/JPS62125347A/en
Publication of JPH052218B2 publication Critical patent/JPH052218B2/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
    • G03C3/00Packages of films for inserting into cameras, e.g. roll-films, film-packs; Wrapping materials for light-sensitive plates, films or papers, e.g. materials characterised by the use of special dyes, printing inks, adhesives

Description

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

[産業上の利用分野] 本発明はフイルム等の写真感光材料の包装体に
関し、詳しく、包装体内に収納されるフイルム等
の写真感光材料にカブリ等の写真性能上の悪影響
を与えない写真感光材料包装体に関する。 [発明の背景] フイルム、印画紙等の写真感光材料の保管、移
送等に用いられる写真フイルムマガジン、パツケ
ージ等の写真感光材料包装体においては、収納す
る写真感光材料の仕様等の文字、美観上の図柄、
さらには水ぬれ、さび等に対する保護等を目的と
して種々の塗装、印刷が施されている。 従来、この塗装、印刷に用いられる塗料や印刷
用インキは、自然乾燥、加熱焼付け、加熱乾燥な
どにより、重合、縮合、硬化等の化学反応を起こ
し、包装体となる金属、紙等の包装体基材上に定
着していた。 これら塗料もしくはインキの中には、乾燥・硬
化が不充分である場合には、包装体内に収納され
るフイルム等の写真感光材料にカブリ等の悪影響
を与えるものがあり、また、硬化度が適性であつ
ても、塗料や印刷インキの種類によつては写真感
光材料の保管、移送期間中に包装体内に収納され
る写真感光材料に前記と同様に悪影響を与えるも
のがあり、このため塗膜の強度、外観等に優れた
性質を有する塗料、印刷用インキ材料でも写真性
能に影響を与えるものは使用することができず、
写真性能上不活性なことを確認するためには使用
する樹脂、添加剤、顔料、溶剤等について個別に
調査を行う必要があつた。従つて、従来の写真感
光材料包装体用の塗料、インキにおいては、写真
性能上不活性な物質で構成された塗料、インキの
組み合わせを選択し、さらに、塗料等を乾燥硬化
度までも管理する必要があり、工程管理が煩雑と
なつてしまう不都合があつた。 [発明の目的] 従つて、本発明の目的は、包装体内に収納され
る写真感光材料にカブリ等の悪影響が発生しな
い、生産性の良い写真感光材料包装体を提供する
ことにある。 [発明の構成] 本発明の上記目的は、表面に写真性能上不活性
な層が設けられている写真感光材料包装体によつ
て達成される。 [発明の具体的構成] 本発明は、フイルム等の写真感光材料の包装体
の表面に写真性能上不活性な層を設ける点に特徴
がある。即ち、該写真性能上不活性な層が、包装
体基材上の塗設層のすべてであつても、包装体基
材上に他の下塗り層として種々の層が設けられた
上の最上層であつても、最終的に包装体の表面に
写真性能上不活性な層が設けられていればよい。 本発明の写真感光材料包装体の表面に設けられ
る写真性能上不活性な層(以下、本発明の表面層
という)は、以下の樹脂で形成されたものであ
る。 本発明の表面層に用いられる樹脂としては、塩
化ビニル樹脂脂(オルガノゾルを含む)を主成分
とするビニル系樹脂(例えば、塩化ビニルを主体
とする共重合樹脂、オルガノゾルとして塩化ビニ
ルを主体とした共重合樹脂を可塑剤と少量の溶剤
中に分散したもの等)、ビニル・アミノ樹脂(例
えば、塩化ビニル、スチレン等のビニル樹脂と、
尿素樹脂、ベンゾグアナミン樹脂などのアミノ基
を有する樹脂とからなる樹脂等)、アルキド・ビ
ニル系樹脂(例えば、無水フタル酸、無水マレイ
ン酸などの多塩基酸類とグリセリン、ペンタエリ
スリトールなどの多価アルコール類との縮合物を
塩化ビニル、スチレン等ビニルモノマーで変性さ
せた樹脂等)、オイルフリ−アルキド樹脂(例え
ば、アルキド樹脂でアマニ油、大豆油、ヒマシ
油、などの脂肪油、脂肪酸で変性させていない樹
脂等)、熱硬化アクリル・アミノ樹脂(例えば、
アクリル酸、メタクリル酸、アクリル酸エステ
ル、アクリルアミド、アクリロニトリルなどのア
クリル樹脂と尿素樹脂、ベンゾグアナミン樹脂な
どのアミノ基を有する樹脂からなる樹脂等)、高
分子および低分子のポリエステル・アミノ樹脂
(例えば、アジピン酸・イソフタル酸などの酸類
とエチレングリコール、トリメチロールプロパン
等の多価アルコール類との重縮合により得られる
ポリエステル樹脂と、尿素樹脂・ベンゾグアナミ
ン樹脂などのアミノ基を有する樹脂とからなる樹
脂等)、さらに、エポキシ、アミノ樹脂等が挙げ
られる。 本発明の表面層に用いられる樹脂は、顔料を添
加しない透明な樹脂として用いることが好ましい
態様であるが、写真性能的に不活性な顔料、例え
ば、キナクリロンレツド、ウオツチングレツド、
不溶性アゾ型、クロムバーミリオン、イソインド
リノン、ぐんじよう、銅フタロシアニングリー
ン、等は用いることができる。 本発明の表面層に用いられる樹脂は、溶剤等に
混合溶解させて、顔料や添加剤とともに分散混合
された塗工剤(以下、本発明の塗工剤という)と
して調整して本発明の包装体の基材上に塗設され
ることができる。 ここで用いられる溶剤としては、トルエン、キ
シレン等の芳香族炭化水素、酢酸エチル等のエス
テル類、アセトン、メチルエチルケトン等のケト
ン類、メタノール、エタノール等のアルコール類
等が挙げられる。 また、その他添加剤としては、写真性能に悪影
響を与えないもので、界面活性剤、皮張り防止
剤、増粘剤、流動性を付与する延展剤が等を用い
ることができる。 本発明の塗工剤層は、塗工された後乾燥、硬化
され、本発明の表面層が形成される。この乾燥、
硬化の条件は、基材の種類、用いられる塗工剤の
種類、ドライヤーの量等により異なるが、乾燥、
硬化温度としては、概ね、常温〜350℃が好まし
く、乾燥、硬化時間としては1秒〜40分程度が好
ましい。 上記の如くして形成される本発明の表面層の膜
厚としては、0.01μm〜100μmが好ましく、さら
に具体的には、塗料として通常の塗工装置により
塗設される場合、0.01μm〜100μmが好ましく、
より好ましくは1μm〜20μmであり、印刷インキ
としてオフセツト印刷機等により印刷される場
合、0.01μm〜10μmが好ましく、より好ましく
は、0.5〜4μmである。 本発明の写真感光材料包装体の基材材料には任
意のものが用いられ、例えば種々の紙類、木材
類、天然あるいは合成高分子等からなるプラスチ
ツク類、鉄類、亜鉛、アルミニウム、銅、それら
の合金等の金属類が挙げられる。また、これらの
基材材料の表面は種々の表面処理が行われていて
もよい。 本発明の写真感光材料包装体においては、前記
した本発明の表面層を有していれば、従来用いら
れている各種の着色塗料等の下塗り層が設けられ
ていてもよい。即ち、これらの下塗り層には、表
面層に出ていなければ写真性能に悪影響を与える
ものであつても、本発明の表面層がその上に設け
られることにより任意のものが用いられる。この
下塗り層に用いられるものは具体的には、種々の
樹脂、溶剤、油脂類、無機および有機顔料の任意
の組み合わせが選択できる。 [発明の具体的効果] 本発明の表面層を有する包装体によれば、内部
に収納される写真感光材料は、長期に保管されて
もカブリを発生せず、包装体の生産工程におい
て、使用する塗装層の素材について個々に写真性
能上の活性、不活性を検査することが省けること
となり工程管理が容易となつて生産性の良い写真
感光材料の包装体が得られることである。 [発明の具体的実施例] 以下、本発明を実施例により具体的に説明する
が本発明の実施の態様はこれらに限定されるもの
ではない。 実施例 1 基板として厚さ0.25mmのテイン(Sn)フリース
チールを用いて、下塗層としてチタンホワイト30
重量部を含有するポリエステルアミノ樹脂から成
る塗料を塗設し180℃、10分間の乾燥を行なつた。
さらに、カーボンブラツク40重量部を含有するロ
ジン変性アルキド樹脂から成る印刷インキを用い
てオフセツト印刷を行なつた後、160℃、10分間
の乾燥を行なつた。続いて、表面層として、顔料
を含有しない透明な塗工剤であるポリエステル・
アミノ樹脂から成る塗料を用いて塗設した後、
190℃、10分間の乾燥と行ない、膜厚15μmの皮膜
層を設けた。 以上のように調製した金属印刷版をASA400の
写真用カラーフイルムと共存させて、55℃、5日
間保管し、後現像処理を行なつた。前記金属印刷
板と共存させずに保管したブランクとの濃度差を
測定し、カブリ濃度を計測した。 実施例 2 実施例1におけ表面層のポリエステルアミノ樹
脂の代わりにオイルフリーアルキド樹脂から成る
表面層をオフセツト印刷にて設けた後、180℃、
10分間の乾燥を行い、膜厚2μmの皮膜層を設け
た。 以上のように調製した金属印刷板を実施例1と
同条件で保管し、カブリ濃度を計測した。 比較例 1 実施例1における表面層の塗料による塗設を行
なわない以外は実施例1と同条件で金属印刷板を
調製し、保管し、カブリ濃度を計測した。 比較例 3〜9 実施例1において表面層のポリエステルアミノ
樹脂を表1(つづき)に示す樹脂に代えた以外は
同様にして比較試料を作成し、同様にカブリ濃度
に計測した。 実施例 3 基紙に厚み200μmの通常紙を用いカーボンブラ
ツク40重量部を含むロジン変性フエノール樹脂印
刷インキによりオフセツト印刷を行ない30℃、10
秒間乾燥を行なつた。 さらに表面層として、顔料を含有しないアクリ
ル・ビニル樹脂塗料を塗設し、常温乾燥を行なつ
た。表面層の膜厚は約1μmであつた。 以上のように調製した紙片をASA400の写真用
カラーフイルムと共存させて55℃、5日間保管し
た後現像処理を行なつた。 前記紙片と共存させずに同条件で保管したブラ
ンクとの濃度差を測定し、カブリ濃度を計測し
た。 比較例 10〜11 実施例3において表面層のアクリル・ビニル樹
脂を表1(つづき)に示す樹脂に代えた以外に同
様にして比較試料を作成し、同様にカブリ濃度を
計測した。 比較例 2 実施例3における表面層の塗設を行なわい以外
は実施例3と同条件で紙片を調製しカブリ濃度を
計測した。 実施例1〜3および比較例1〜11の結果を下記
表1および表1(つづき)に示す。
[Industrial Field of Application] The present invention relates to a package for photographic light-sensitive materials such as films, and more specifically, a photographic light-sensitive material that does not adversely affect photographic performance such as fog on the photographic light-sensitive materials such as films stored in the package. Regarding packaging. [Background of the Invention] In photographic material packages such as photographic film magazines and package cases used for storing and transporting photographic materials such as films and photographic paper, there is a need for text and aesthetics such as specifications of the photographic materials to be stored. The design of
Furthermore, various coatings and printings are applied to protect against water, rust, etc. Conventionally, paints and printing inks used for painting and printing undergo chemical reactions such as polymerization, condensation, and hardening through natural drying, heat baking, heat drying, etc. It was fixed on the base material. Some of these paints or inks may have an adverse effect such as fogging on photographic materials such as film stored in the package if drying and curing are insufficient. However, depending on the type of paint or printing ink, there are some that have the same negative effect on the photographic material stored in the packaging during storage and transportation of the photographic material. Paints and printing ink materials that have excellent properties such as strength and appearance cannot be used if they affect photographic performance.
In order to confirm that they are inert in terms of photographic performance, it was necessary to individually investigate the resins, additives, pigments, solvents, etc. used. Therefore, in conventional paints and inks for photographic material packaging, combinations of paints and inks made of substances that are inert in terms of photographic performance are selected, and the degree of drying and curing of the paints, etc. is also controlled. However, there was an inconvenience in that process control became complicated. [Object of the Invention] Accordingly, an object of the present invention is to provide a photographic material package with good productivity, which does not cause adverse effects such as fog on the photographic material housed in the package. [Structure of the Invention] The above-mentioned object of the present invention is achieved by a photographic light-sensitive material package whose surface is provided with a layer that is inactive in terms of photographic performance. [Specific Structure of the Invention] The present invention is characterized in that a layer that is inactive in terms of photographic performance is provided on the surface of a package of a photographic light-sensitive material such as a film. That is, even if the photographically inactive layer is all of the coating layers on the package base material, it may be the uppermost layer on which various layers are provided as other undercoat layers on the package base material. However, it is sufficient that a layer that is inactive in terms of photographic performance is finally provided on the surface of the package. The photographically inert layer provided on the surface of the photographic light-sensitive material package of the present invention (hereinafter referred to as the surface layer of the present invention) is formed of the following resin. The resin used for the surface layer of the present invention includes vinyl resins whose main component is vinyl chloride resin (including organosol) (e.g., copolymer resins whose main component is vinyl chloride, and organosols whose main component is vinyl chloride). Copolymer resins dispersed in a plasticizer and a small amount of solvent, etc.), vinyl amino resins (e.g., vinyl resins such as vinyl chloride, styrene, etc.),
resins with amino groups such as urea resins and benzoguanamine resins), alkyd/vinyl resins (e.g., polybasic acids such as phthalic anhydride and maleic anhydride, and polyhydric alcohols such as glycerin and pentaerythritol) resins modified with vinyl monomers such as vinyl chloride and styrene), oil-free alkyd resins (e.g., alkyd resins that are not modified with fatty oils or fatty acids such as linseed oil, soybean oil, and castor oil) resin, etc.), thermosetting acrylic/amino resin (e.g.
Resins consisting of acrylic resins such as acrylic acid, methacrylic acid, acrylic esters, acrylamide, acrylonitrile, and resins with amino groups such as urea resins and benzoguanamine resins), high-molecular and low-molecular polyester/amino resins (e.g. adipine) (resins made of polyester resins obtained by polycondensation of acids such as acids and isophthalic acids with polyhydric alcohols such as ethylene glycol and trimethylolpropane, and resins having amino groups such as urea resins and benzoguanamine resins), Further examples include epoxy and amino resins. The resin used in the surface layer of the present invention is preferably used as a transparent resin without adding pigments, but pigments that are inert in terms of photographic performance, such as quinacrylon red, watching red, etc.
Insoluble azo type, chrome vermilion, isoindolinone, Gunjiyo, copper phthalocyanine green, etc. can be used. The resin used for the surface layer of the present invention is mixed and dissolved in a solvent, etc., and prepared as a coating agent (hereinafter referred to as the coating agent of the present invention) in which the resin is dispersed and mixed with pigments and additives. It can be coated onto a body substrate. Examples of the solvent used here include aromatic hydrocarbons such as toluene and xylene, esters such as ethyl acetate, ketones such as acetone and methyl ethyl ketone, and alcohols such as methanol and ethanol. Other additives that do not adversely affect photographic performance include surfactants, anti-skinning agents, thickeners, and spreading agents that impart fluidity. After being applied, the coating agent layer of the present invention is dried and cured to form the surface layer of the present invention. This drying,
Curing conditions vary depending on the type of substrate, type of coating agent used, amount of dryer, etc., but drying,
The curing temperature is preferably about room temperature to 350°C, and the drying and curing time is preferably about 1 second to 40 minutes. The thickness of the surface layer of the present invention formed as described above is preferably 0.01 μm to 100 μm, and more specifically, when applied as a paint using a common coating device, the thickness is 0.01 μm to 100 μm. is preferable,
More preferably, it is 1 μm to 20 μm, and when printing as a printing ink with an offset printer or the like, it is preferably 0.01 μm to 10 μm, and more preferably 0.5 to 4 μm. Any base material can be used for the photographic material package of the present invention, such as various papers, woods, plastics made of natural or synthetic polymers, iron, zinc, aluminum, copper, etc. Examples include metals such as alloys thereof. Furthermore, the surfaces of these base materials may be subjected to various surface treatments. In the photographic light-sensitive material package of the present invention, as long as it has the above-described surface layer of the present invention, an undercoat layer such as various conventionally used colored paints may be provided. That is, any undercoat layer can be used as the undercoat layer, even if it would have an adverse effect on the photographic performance if it did not appear on the surface layer, as long as the surface layer of the present invention is provided thereon. Specifically, any combination of various resins, solvents, oils and fats, and inorganic and organic pigments can be selected for use in this undercoat layer. [Specific Effects of the Invention] According to the package having the surface layer of the present invention, the photographic material stored inside does not fog even when stored for a long period of time, and can be easily used in the production process of the package. This eliminates the need to individually inspect the materials of the coating layer for activity or inactivity in terms of photographic performance, which simplifies process control and provides packaging for photographic light-sensitive materials with good productivity. [Specific Examples of the Invention] Hereinafter, the present invention will be specifically explained using Examples, but the embodiments of the present invention are not limited thereto. Example 1 Using 0.25 mm thick tin (Sn) free steel as the substrate, Titanium White 30 was used as the undercoat layer.
A paint consisting of a polyester amino resin containing 100% by weight was applied and dried at 180°C for 10 minutes.
Further, offset printing was performed using a printing ink made of a rosin-modified alkyd resin containing 40 parts by weight of carbon black, followed by drying at 160° C. for 10 minutes. Next, the surface layer is made of polyester, a transparent coating agent that does not contain pigments.
After coating with a paint made of amino resin,
Drying was performed at 190°C for 10 minutes to form a film layer with a thickness of 15 μm. The metal printing plate prepared as described above was stored together with an ASA400 photographic color film at 55° C. for 5 days, and then subjected to post-development. The difference in density between the metal printing plate and a blank stored without coexistence was measured, and the fog density was measured. Example 2 A surface layer made of oil-free alkyd resin was provided in place of the polyester amino resin of the surface layer in Example 1 by offset printing, and then heated at 180°C.
Drying was performed for 10 minutes to form a film layer with a thickness of 2 μm. The metal printing plate prepared as described above was stored under the same conditions as in Example 1, and the fog density was measured. Comparative Example 1 A metal printing plate was prepared and stored under the same conditions as in Example 1, except that the surface layer was not coated with a paint, and the fog density was measured. Comparative Examples 3 to 9 Comparative samples were prepared in the same manner as in Example 1 except that the polyester amino resin in the surface layer was replaced with the resin shown in Table 1 (continued), and the fog density was measured in the same manner. Example 3 Regular paper with a thickness of 200 μm was used as the base paper, and offset printing was performed using a rosin-modified phenolic resin printing ink containing 40 parts by weight of carbon black at 30°C for 10 minutes.
Drying was performed for seconds. Furthermore, a pigment-free acrylic/vinyl resin paint was applied as a surface layer and dried at room temperature. The thickness of the surface layer was approximately 1 μm. The paper pieces prepared as described above were stored together with ASA400 photographic color film at 55°C for 5 days, and then developed. The fog density was measured by measuring the difference in density from a blank stored under the same conditions without coexisting with the paper piece. Comparative Examples 10 to 11 Comparative samples were prepared in the same manner as in Example 3 except that the acrylic/vinyl resin in the surface layer was replaced with the resin shown in Table 1 (continued), and the fog density was measured in the same manner. Comparative Example 2 A piece of paper was prepared under the same conditions as in Example 3, except that the surface layer in Example 3 was not applied, and the fog density was measured. The results of Examples 1 to 3 and Comparative Examples 1 to 11 are shown in Table 1 and Table 1 (continued) below.

【表】【table】

【表】 以上の結果から金属および紙基材の表面に本発
明の表面層を設けた試料では、その下塗層にカブ
リの生じる塗膜(比較1および2)が設けられて
いても何らその影響を写真感光材料に及ぼすこと
がなく、55℃、5日間という保管期間にあつても
カブリの程度を増加させていない。
[Table] From the above results, in the samples in which the surface layer of the present invention was provided on the surface of metal and paper base materials, even if the undercoat layer was provided with a coating film that caused fog (Comparisons 1 and 2), there was no problem. It has no effect on photographic materials and does not increase the degree of fogging even during storage at 55°C for 5 days.

Claims (1)

【特許請求の範囲】[Claims] 1 塩化ビニルを主体とする共重合樹脂、ビニ
ル・アミノ樹脂、アルキド・ビニル系樹脂、オイ
ルフリーアルキド樹脂、熱硬化アクリル・アミノ
樹脂または高分子および低分子のポリエステル・
アミノ樹脂からなる塗布液を表面に塗工すること
により写真性能上不活性な層が設けられているこ
とを特徴とする写真感光材料包装体。
1. Copolymer resins mainly composed of vinyl chloride, vinyl/amino resins, alkyd/vinyl resins, oil-free alkyd resins, thermosetting acrylic/amino resins, or high- and low-molecular polyesters.
1. A photographic material package, characterized in that a layer inert in terms of photographic performance is provided by coating the surface with a coating liquid made of an amino resin.
JP26589785A 1985-11-26 1985-11-26 Package of photographic sensitive material Granted JPS62125347A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP26589785A JPS62125347A (en) 1985-11-26 1985-11-26 Package of photographic sensitive material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP26589785A JPS62125347A (en) 1985-11-26 1985-11-26 Package of photographic sensitive material

Publications (2)

Publication Number Publication Date
JPS62125347A JPS62125347A (en) 1987-06-06
JPH052218B2 true JPH052218B2 (en) 1993-01-12

Family

ID=17423621

Family Applications (1)

Application Number Title Priority Date Filing Date
JP26589785A Granted JPS62125347A (en) 1985-11-26 1985-11-26 Package of photographic sensitive material

Country Status (1)

Country Link
JP (1) JPS62125347A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01312537A (en) * 1988-06-13 1989-12-18 Konica Corp Cartridge for photographic film

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS544932A (en) * 1977-06-15 1979-01-16 Fuji Kiki Kougiyou Kk Bonding agent for lighttshield portion of photoofilm container
JPS55140835A (en) * 1979-04-19 1980-11-04 Fuji Photo Film Co Ltd Light shielding paper for roll photographic film
JPS56135839A (en) * 1980-03-26 1981-10-23 Konishiroku Photo Ind Co Ltd Photographic product
JPS6026063A (en) * 1983-07-25 1985-02-08 Fuji Photo Film Co Ltd Paint for film cartridge made of metal
JPS6026061A (en) * 1983-07-25 1985-02-08 Fuji Photo Film Co Ltd Paint for film cartridge made of metal
JPS6026062A (en) * 1983-07-25 1985-02-08 Fuji Photo Film Co Ltd Paint for film cartridge made of metal
JPS6029743A (en) * 1983-07-09 1985-02-15 Fuji Photo Film Co Ltd Packaging material for photosensitive material and its molded body
JPS60196335A (en) * 1984-03-21 1985-10-04 富士写真フイルム株式会社 Laminated film

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS544932A (en) * 1977-06-15 1979-01-16 Fuji Kiki Kougiyou Kk Bonding agent for lighttshield portion of photoofilm container
JPS55140835A (en) * 1979-04-19 1980-11-04 Fuji Photo Film Co Ltd Light shielding paper for roll photographic film
JPS56135839A (en) * 1980-03-26 1981-10-23 Konishiroku Photo Ind Co Ltd Photographic product
JPS6029743A (en) * 1983-07-09 1985-02-15 Fuji Photo Film Co Ltd Packaging material for photosensitive material and its molded body
JPS6026063A (en) * 1983-07-25 1985-02-08 Fuji Photo Film Co Ltd Paint for film cartridge made of metal
JPS6026061A (en) * 1983-07-25 1985-02-08 Fuji Photo Film Co Ltd Paint for film cartridge made of metal
JPS6026062A (en) * 1983-07-25 1985-02-08 Fuji Photo Film Co Ltd Paint for film cartridge made of metal
JPS60196335A (en) * 1984-03-21 1985-10-04 富士写真フイルム株式会社 Laminated film

Also Published As

Publication number Publication date
JPS62125347A (en) 1987-06-06

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