JPS6251475A - Matte film - Google Patents

Matte film

Info

Publication number
JPS6251475A
JPS6251475A JP60191157A JP19115785A JPS6251475A JP S6251475 A JPS6251475 A JP S6251475A JP 60191157 A JP60191157 A JP 60191157A JP 19115785 A JP19115785 A JP 19115785A JP S6251475 A JPS6251475 A JP S6251475A
Authority
JP
Japan
Prior art keywords
film
resin
acrylic polyol
matte
glass transition
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
JP60191157A
Other languages
Japanese (ja)
Other versions
JPH0651388B2 (en
Inventor
Yasuo Kuriyama
靖夫 栗山
Kenji Watanabe
健司 渡辺
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.)
Kimoto Co Ltd
Original Assignee
Kimoto Co Ltd
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 Kimoto Co Ltd filed Critical Kimoto Co Ltd
Priority to JP60191157A priority Critical patent/JPH0651388B2/en
Publication of JPS6251475A publication Critical patent/JPS6251475A/en
Publication of JPH0651388B2 publication Critical patent/JPH0651388B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/50Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
    • B41M5/52Macromolecular coatings
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/50Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
    • B41M5/502Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording characterised by structural details, e.g. multilayer materials
    • B41M5/508Supports
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/50Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
    • B41M5/52Macromolecular coatings
    • B41M5/5218Macromolecular coatings characterised by inorganic additives, e.g. pigments, clays
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/50Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
    • B41M5/52Macromolecular coatings
    • B41M5/5227Macromolecular coatings characterised by organic non-macromolecular additives, e.g. UV-absorbers, plasticisers, surfactants
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/50Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
    • B41M5/52Macromolecular coatings
    • B41M5/5254Macromolecular coatings characterised by the use of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. vinyl polymers

Landscapes

  • Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
  • Duplication Or Marking (AREA)
  • Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
  • Laminated Bodies (AREA)

Abstract

PURPOSE:To enhance the impact resistance of a matte layer, by using a specific acrylic polyol resin, a cellulosic resin and an isocyanate prepolymer as a binder. CONSTITUTION:A matte layer containing an acrylic polyol resin with a glass transition temp. of 40-65 deg.C, a cellulosic resin, an isocyanate polymer and a matte agent is provided on a plastic film support. By this method, the matte layer, wherein the impact resistance of a film is improved and adhesiveness, surface hardness, solvent resistance, curl stability and heat stability heretofore required are good and an effect on a ziazo photosensitive layer is reduced, is obtained. In this case, if the acrylic polyol resin with a glass transition temp. of 40 deg.C or less is used, film hardness is increased and a drying property becomes inferior and, if one with a glass transition temp. of 65 deg.C or more is used, the impact resistance of the film is inferior and a crack easily develops on the film.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明はマットフィルムに関し、更に詳細には製図用ト
ラフティングフィルム、PPC用転写フィルム、ジアゾ
複写用第2原図フィルム等の支持体として使用されるマ
ットフィルムに関するものである。
[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a matte film, and more specifically, it is used as a support for drafting trafting films, PPC transfer films, second original film for diazo copying, etc. This relates to a matte film.

〔従来の技術〕[Conventional technology]

マントフィルムは一般にプラスチックフィルム支持体に
樹脂バインダー及びマット剤として、シリカ粉、アルミ
ナ粉等の顔料を含むマント剤を設けたもので、バインダ
ーとしては例えば、アクリル樹脂、塩化ビニル−酢酸ビ
ニル共重合体等のビニル系熱可塑性樹脂(特開昭50−
136363号、特公昭50−1152号等)やメラミ
ン樹脂、フェノール樹脂等のホルムアルデヒド系熱硬化
性樹脂(特開昭50−38771号、同50−1416
83号等)や熱硬化型ウレタン樹脂(特開昭60−12
9257号)が知られている。
Mantle film is generally a plastic film support with a resin binder and a mantle agent containing a pigment such as silica powder or alumina powder as a matting agent.The binder is, for example, an acrylic resin, vinyl chloride-vinyl acetate copolymer. Vinyl thermoplastic resins such as
136363, Japanese Patent Publication No. 50-1152, etc.), formaldehyde thermosetting resins such as melamine resin, phenol resin (Japanese Patent Publication No. 50-38771, Japanese Patent Publication No. 50-1416, etc.)
No. 83, etc.) and thermosetting urethane resins (JP-A-60-12)
No. 9257) is known.

このようなマントフィルムは製図用トラフティングフィ
ルム、PPC(静電複写機)用転写フィルム、ジアゾ複
写用第2原図フィルムの支持体等として用いられるので
、特に使用中、眉間剥離を生じないようなマット層の支
持体に対する接着性が良いこと、使用中又は加筆時に傷
がつかないよう高い表面硬度を有すること、転写フィル
ムとして用いた場合はトナー画像の修正液(有機溶剤使
用)に侵されないよう耐溶剤性を備えると共に、トナー
画像の熱定着時に異臭を発生したり変色しないよう熱安
定性を備えること、品質上の点からは勿論、複写機内で
の重送やジャム(IF、づまり)防止の点からも使用中
又は保存中、カールの発生が少ないこと(カール安定性
が良いこと)、第2原図フィルムの支持体として用いた
場合は保存中、画像濃度低下等、ジアゾ感光層への影響
が少ないこと等は従来より要求される性能であるが、そ
れに加えて取扱い中に折れ、ベコ等からくる衝撃により
マント層にクランクが生じたり、白化したりすることに
よって、成果品としての商品価値を著しく低下させない
ような耐衝撃性のある性能が要求される。
This kind of cloak film is used as a support for trafting film for drafting, transfer film for PPC (electrostatic copying machine), second original film for diazo copying, etc., so it is especially suitable for preventing peeling between the eyebrows during use. The matte layer should have good adhesion to the support, high surface hardness to prevent scratches during use or addition, and should not be attacked by toner image correction fluid (organic solvent used) when used as a transfer film. In addition to being solvent resistant, the toner image must also be thermally stable so that it does not generate strange odors or discolor when it is heat-fixed, and from a quality standpoint, it also prevents double feeding and jams (IF) in the copying machine. In terms of this, there should be little curling during use or storage (good curl stability), and when used as a support for the second original film, there should be no risk of damage to the diazo photosensitive layer, such as a decrease in image density, during storage. Although the performance has been traditionally required to be less affected, in addition to this, the mantle layer may crack or turn white due to bending during handling, impact from bevels, etc. It is required to have impact resistance that does not significantly reduce its value.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

しかし従来のマットフィルムにおいては、これらの性能
を同時に満足するものではなく、例えば、バインダーと
してビニル系熱可塑性樹脂を用いたものは支持体に対す
る接着性及び耐溶剤性に劣る。
However, conventional matte films do not satisfy these properties at the same time; for example, those using a vinyl thermoplastic resin as a binder have poor adhesion to a support and poor solvent resistance.

またホルムアルデヒド系熱硬化性樹脂を用いたものはト
ナー画像の熱定着時に刺戟具のあるホルムアルデヒドガ
スを発生して作業環境を悪くする。
Further, those using formaldehyde-based thermosetting resins generate irritating formaldehyde gas during heat fixing of toner images, making the work environment worse.

またガラス転移温度の高い(70℃以上)アクリルポリ
オール樹脂とイソシアネート系熱硬化性樹脂を用いた場
合はマット層にクラックが生じやすく折れ、ベコに対し
て白化現像が見られ、著しく商品価値を低下させるとい
う欠点があった。
Additionally, when using acrylic polyol resins and isocyanate thermosetting resins that have a high glass transition temperature (70°C or higher), the matte layer tends to crack and break, and whitening can be seen on the surface, significantly reducing the product value. It had the disadvantage of letting you do it.

〔問題点を解決するための手段〕[Means for solving problems]

本発明は上記の如き従来技術の問題点を解消することの
できるマットフィルムを提供することを目的として創案
されたものであり、取扱い作業時における折れ、ベコ等
の衝撃からくるマット層の耐クラツク性の付与であり、
同時に従来から要求されている接着性、表面硬度、耐溶
剤性、カール安定性及び熱安定性共に満足すると共に、
ジアゾ感光層への影響も少ないマットフィルムを提供す
ることであり、プラスチックフィルム支持体上に、ガラ
ス転移温度40〜65℃のアクリルポリオール樹脂と繊
維素系樹脂とイソシアネートプレポリマーとマント剤と
を含む被覆層を設けたことを特徴とするものである。
The present invention was devised for the purpose of providing a matte film that can solve the problems of the prior art as described above. It is the imparting of sex,
At the same time, it satisfies the conventional requirements of adhesion, surface hardness, solvent resistance, curl stability, and thermal stability.
The object of the present invention is to provide a matte film that has little influence on the diazo photosensitive layer, and contains an acrylic polyol resin with a glass transition temperature of 40 to 65°C, a cellulose resin, an isocyanate prepolymer, and a mantle agent on a plastic film support. It is characterized by providing a covering layer.

〔発明の構成〕[Structure of the invention]

本発明のマットフィルムはプラスチックフィルム支持体
上にガラス転移温度(Tg)が40〜65℃のアクリル
ポリオール樹脂と繊維素系樹脂とイソシアネートプレポ
リマーとマット剤とを含むマット層を設けたことを特徴
とするものである。
The matte film of the present invention is characterized in that a matte layer containing an acrylic polyol resin with a glass transition temperature (Tg) of 40 to 65°C, a cellulose resin, an isocyanate prepolymer, and a matting agent is provided on a plastic film support. That is.

本発明で用いられるアクリルポリオール樹脂はヒドロキ
シ基含有モノマーと他の重合性上ツマ−との共重合体で
あってイソシアネートプレポリマーと共に熱硬化性ポリ
ウレタン樹脂の材料である。
The acrylic polyol resin used in the present invention is a copolymer of a hydroxy group-containing monomer and other polymerizable polymers, and together with an isocyanate prepolymer, is a material for a thermosetting polyurethane resin.

塗膜の耐衝撃性を改善せしめ、且つ、従来がら要求され
ている接着性、表面硬度、耐溶剤性、カール安定性及び
熱安定性が良く、ジアゾ感光層への影響の少ないマット
層を得るべく種々研究を重ねた結果、本発明者らはガラ
ス転移温度(Tg)が40〜65℃のアクリルポリオー
ル樹脂と繊維素系樹脂を併用することによって満足のい
く結果を見いだしたが、好ましくは、ガラス転移温度(
Tg)が50〜60℃のアクリルポリオール樹脂である
Improve the impact resistance of the coating film, and obtain a matte layer that has the conventionally required adhesion, surface hardness, solvent resistance, curl stability, and thermal stability, and has little effect on the diazo photosensitive layer. As a result of various studies, the present inventors have found satisfactory results by using an acrylic polyol resin with a glass transition temperature (Tg) of 40 to 65°C in combination with a cellulose resin. Preferably, Glass-transition temperature(
It is an acrylic polyol resin with a Tg) of 50 to 60°C.

ガラス転移温度(Tg)が40’C以下のアクリルポリ
オール樹脂を使用した場合は、塗膜硬度が低く乾燥性が
悪くなるという欠点がある。
When an acrylic polyol resin having a glass transition temperature (Tg) of 40'C or less is used, there is a drawback that the hardness of the coating film is low and the drying properties are poor.

また、ガラス転移温度(Tg)が65℃以上のアクリル
ポリオール樹脂を使用した場合は、塗膜の耐衝撃性が劣
り、塗膜にクラックが生じやすい。
Furthermore, when an acrylic polyol resin having a glass transition temperature (Tg) of 65° C. or higher is used, the impact resistance of the coating film is poor and cracks are likely to occur in the coating film.

本発明で使用するガラス転移温度(’rg )が50〜
60℃のアクリルポリオール樹脂は、例えば、日本ライ
ヒホールドー〇商品名アクリデックA304.A311
等がある。
The glass transition temperature ('rg) used in the present invention is 50~
The 60°C acrylic polyol resin is, for example, Nippon Reichhold Co., Ltd. (trade name: Acrydec A304. A311
etc.

アクリルポリオール樹脂と併用される繊維素系樹脂とし
ては硝酸繊維素樹脂、酢酸繊維素樹脂、酢酸繊維素樹脂
、プロピオン酸繊維素樹脂等があるが、樹脂の溶解性及
び、アクリルポリオール樹脂との相溶性の点から最も好
ましいのは、硝酸繊維素樹脂で、硝化度及び秒数(粘度
)に関係なく使用することができるが、塗工液の調整等
の作業性からみて1/8〜10秒(粘度)のものが好ま
しい。
Examples of cellulose resins used in combination with acrylic polyol resins include nitrate cellulose resin, acetic acid cellulose resin, acetic acid cellulose resin, and propionate cellulose resin, but the solubility of the resin and compatibility with the acrylic polyol resin may vary. In terms of solubility, the most preferred is nitrate cellulose resin, which can be used regardless of the degree of nitrification and the number of seconds (viscosity), but from the viewpoint of workability such as adjusting the coating liquid, it is 1/8 to 10 seconds. (viscosity) is preferred.

硝酸繊維素樹脂の使用量は、アクリルポリオール100
  重量部に対して15〜65重量部で、好ましくは2
5〜45重量部である。
The amount of nitrate cellulose resin used is 100% of the acrylic polyol.
15 to 65 parts by weight, preferably 2 parts by weight
It is 5 to 45 parts by weight.

65重量部以上加えると、塗膜の接着性、耐溶剤   
    性が劣り、15重量以下だと、塗膜の硬度が劣
り、製図用フィルムとして使用した場合、鉛筆の消去性
に劣るので好ましくない。
Adding 65 parts by weight or more will improve the adhesion and solvent resistance of the coating.
If the weight is less than 15%, the hardness of the coating film will be poor, and when used as a drafting film, the erasability of a pencil will be poor, which is not preferable.

一方、イソシアネートプレポリマーには脂肪族と芳香族
イソシアネートプレポリマーがあり、前者にはへキサメ
チレンジイソシアネート(HMDI)その誘導体、後者
にはトリレンジイソシアネート(TDI ) 、キシレ
ンジイソシアネート(XDI )等が挙げられる。
On the other hand, isocyanate prepolymers include aliphatic and aromatic isocyanate prepolymers, the former including hexamethylene diisocyanate (HMDI) and its derivatives, and the latter including tolylene diisocyanate (TDI), xylene diisocyanate (XDI), etc. .

商品名としては、成田薬品工業社のタケネー)D102
 、D202 、DIION、日本ポリウレタン工業社
のコロネートし、コロネートHし、日本ライヒホールド
社のパーノックDN950.  D750等の商品が挙
げられる。
The product name is Narita Pharmaceutical Co., Ltd.'s Takene) D102.
, D202, DIION, Coronate, Coronate H from Nippon Polyurethane Industries, Parnock DN950 from Nippon Reichhold. Examples include products such as D750.

アクリルポリオール樹脂とイソシアネートプレポリマー
の混合割合は当量比(NGOloH)で、0.8〜2.
0、好ましくは1.0〜1.6である。
The mixing ratio of the acrylic polyol resin and the isocyanate prepolymer is an equivalent ratio (NGOloH) of 0.8 to 2.
0, preferably 1.0 to 1.6.

0.8未満では接着性、耐溶剤性が不充分であり、また
、2.0を越えると塗膜にクラックが生じやすく、耐衝
撃性に劣るので好ましくない。
If it is less than 0.8, the adhesion and solvent resistance will be insufficient, and if it exceeds 2.0, the coating film will tend to crack and have poor impact resistance, which is not preferred.

マント剤としては、シリカ、ガラス、アルミナ、酸化チ
タン等の粉末が使用される。
As the mantle agent, powders of silica, glass, alumina, titanium oxide, etc. are used.

使用量は全樹脂固型分100重量部に対し30〜200
重量部程度が適当である。
The amount used is 30 to 200 parts by weight per 100 parts by weight of the total resin solid content.
Parts by weight are appropriate.

支持体としてはポリエステル、ポリカーボネート、セル
ロースアセテート、ポリイミド等のフィルムが使用され
る。
As the support, films of polyester, polycarbonate, cellulose acetate, polyimide, etc. are used.

又、使用目的に於いては、酸化チタン、シリカ等を混入
した練込みフィルムの使用もできる。
Depending on the purpose of use, a kneaded film containing titanium oxide, silica, etc. can also be used.

厚さは使用目的によって若干具なるが、一般に25〜2
00μ程度が適当である。
The thickness varies slightly depending on the purpose of use, but generally 25 to 2
Approximately 00μ is appropriate.

マット層の厚さは使用目的により異なるが、一般に5〜
15μ程度が適当である。
The thickness of the matte layer varies depending on the purpose of use, but is generally 5~
Approximately 15μ is appropriate.

また、塗工用有機溶剤としては、ケトン(例えばアセト
ン、メチルエチルケトン、メチルイソブチルケトン、シ
クロヘキサノン)、エステル(例えばメチルアセテート
、エチルアセテート、ブチルアセテート、グリコールア
セテート、モノエチルエーテル)、芳香族炭化水素(例
えば、ベンゼントルエン、キシレン)等のOH基のない
ものが好ましい。
In addition, organic solvents for coating include ketones (e.g. acetone, methyl ethyl ketone, methyl isobutyl ketone, cyclohexanone), esters (e.g. methyl acetate, ethyl acetate, butyl acetate, glycol acetate, monoethyl ether), aromatic hydrocarbons (e.g. , benzenetoluene, xylene) and the like are preferred.

〔実施例〕〔Example〕

以下、本発明の実施例を示す。 Examples of the present invention will be shown below.

尚、部1%は、重量基準である。 実施例及び比較例に
使用した樹脂、顔料等を表−1にまとめて列記する。
Incidentally, part 1% is based on weight. Resins, pigments, etc. used in Examples and Comparative Examples are listed in Table 1.

表−1※Tgニガラス転移温度 実施例、比較例°の処方は表−2の通りである。Table-1 *Tg glass transition temperature The formulations of Examples and Comparative Examples are shown in Table 2.

表−2 表−2のアクリルポリオール/硝化綿の重量比、NGO
loHの当量比は下記の通りである。
Table-2 Weight ratio of acrylic polyol/nitrified cotton in Table-2, NGO
The loH equivalent ratio is as follows.

※NC010H:  イソシアネートプレポリマーのN
CO基とアクリルポリオール 樹脂のOH基の比率 前記組成物(但し、タケネー)DIION及びニーパン
22Rを除く)をボールミルで24時間混合分散した後
、所定量のタケネー1−D ll0N (実施例1.2
. 比較例1.2.3)ニーパン22R(比較例4)を
添加して、マント層形成用塗料とし、これを50μ厚の
ポリエステルフィルム上に乾燥後の厚さが8μとなるよ
う塗工し、120℃で1分間乾燥し、更に150℃で5
分間熱処理を行って塗膜を硬化せしめ、マット層を形成
することによりマットフィルムを作成した。
*NC010H: N of isocyanate prepolymer
Ratio of CO group to OH group of acrylic polyol resin After mixing and dispersing the above composition (excluding Takene DIION and Kneepan 22R) in a ball mill for 24 hours, a predetermined amount of Takene 1-D ll0N (Example 1.2
.. Comparative Example 1.2.3) Kneepan 22R (Comparative Example 4) was added to make a coating for forming a cloak layer, and this was coated on a 50μ thick polyester film so that the thickness after drying was 8μ, Dry at 120℃ for 1 minute, then dry at 150℃ for 5 minutes.
A matte film was prepared by heat-treating for a minute to cure the coating film and form a matte layer.

次ニ、以上の各マントフィルムについて耐衝撃性、接着
性、表面硬度、耐溶剤性、カール安定性、熱安定性、ジ
アゾ感光層への影響(第2厚図フィルムとして保存後の
画像濃度低下で評価)を試験した。 その結果を表−3
に示す。
Second, impact resistance, adhesion, surface hardness, solvent resistance, curl stability, thermal stability, and influence on the diazo photosensitive layer for each of the above cloak films (decreased image density after storage as a 2nd thick film) (evaluation) was tested. Table 3 shows the results.
Shown below.

表−3 耐衝撃性;サンプルを10回手でもみマット層面に生じ
たクラックの状態を目視にて観察 O:外観上支障無し ×:外観上支障有り 接着性 ;サンプルを10回手でもみマット層面にセロ
ハンテープを貼った後引剥し、マ ット層の剥離状態を、5を剥離なし、 1を全面剥離として5段階法で評価す る。
Table-3 Impact resistance: The sample was rubbed by hand 10 times, and the state of cracks that occurred on the mat layer surface was visually observed. O: There was no problem in appearance. After applying cellophane tape to the layer surface, it is peeled off, and the peeling state of the matte layer is evaluated on a five-point scale, with 5 being no peeling and 1 being total peeling.

表面硬度、 J r 55400鉛筆硬度試験による。Surface hardness, according to Jr 55400 pencil hardness test.

耐溶剤性;MEKをしみ込ませた綿で、マット層表面を
支持体面が現れるまでこすった 回数。
Solvent resistance: Number of times the surface of the mat layer was rubbed with MEK-impregnated cotton until the support surface appeared.

熱安定性;市販のRPC複写機を用いてサンプルに連続
的に画像転写及び熱定着を行っ た時のホルムアルデヒド臭の有無。
Thermal stability: presence or absence of formaldehyde odor when images are continuously transferred and thermally fixed to a sample using a commercially available RPC copying machine.

○:ホルムアルデヒド臭無し X:ホルムアルデヒド臭有り 保存後の画像濃度低下; サンプルの支持体側にジアゾ感光液を 塗工乾燥してジアゾ感光層を設けて第 2原図フィルムとし、これをマット層 とジアゾ層とが相接するように2枚重 ねて50℃、80%RHの環境下に3日間保存した後、
市販のジアゾ複写機で複 写した時の保存前との画像濃度差。
○: No formaldehyde odor After stacking two sheets so that they are in contact with each other and storing them in an environment of 50°C and 80% RH for 3 days,
Difference in image density when copying with a commercially available diazo copying machine and before storage.

カール試験A; サンプル(50cm X 50cm )を20℃、60
%RHの環境下に30日間放置後、カール性を測定。+
はマント面が凹、−はマ ント面が凸、値は支持台からの最大距 島廿(嘗N)を示す。
Curl test A: sample (50cm x 50cm) at 20℃, 60℃
Curling properties were measured after being left in an environment of %RH for 30 days. +
indicates that the cloak surface is concave, - indicates that the cloak surface is convex, and the value indicates the maximum distance (N) from the support platform.

○:3u以下 △ :  4〜9 l璽 ×:10關以上 カール試験B; サンプル(50cm X 50 cm )を70℃の環
境下に1分間放置後、カール性を測定。
○: 3 u or less △: 4 to 9 l ×: 10 mm or more Curl test B: The sample (50 cm x 50 cm) was left in an environment of 70° C. for 1 minute, and then the curling property was measured.

評価はカール試験Aに同じ。The evaluation is the same as curl test A.

〔効果〕〔effect〕

以上の説明から明らかなように、本発明のマントフィル
ムはバインダーとして特定のアクリルポリオール樹脂と
繊維素系樹脂とイソシアネートプレポリマーを用いる事
によってマット層の耐衝撃性を著しく向上させたばかり
でなく、従来から要求されている接着性、表面硬度、耐
溶剤性、カール安定性、ジアゾ感光層との影響も少ない
等、いずれも充分満足することができた。
As is clear from the above description, the cloak film of the present invention not only significantly improves the impact resistance of the mat layer by using a specific acrylic polyol resin, cellulose resin, and isocyanate prepolymer as binders, but also All of the requirements for adhesiveness, surface hardness, solvent resistance, curl stability, and little influence on the diazo photosensitive layer were fully satisfied.

Claims (1)

【特許請求の範囲】[Claims] プラスチックフィルム支持体上に、ガラス転移温度40
〜65℃のアクリルポリオール樹脂と繊維素系樹脂とイ
ソシアネートプレポリマーとマット剤とを含む被覆層を
設けてなるマットフィルム。
On a plastic film support, a glass transition temperature of 40
A matte film comprising a coating layer containing an acrylic polyol resin at ~65°C, a cellulose resin, an isocyanate prepolymer, and a matting agent.
JP60191157A 1985-08-30 1985-08-30 Matte film Expired - Lifetime JPH0651388B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60191157A JPH0651388B2 (en) 1985-08-30 1985-08-30 Matte film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60191157A JPH0651388B2 (en) 1985-08-30 1985-08-30 Matte film

Publications (2)

Publication Number Publication Date
JPS6251475A true JPS6251475A (en) 1987-03-06
JPH0651388B2 JPH0651388B2 (en) 1994-07-06

Family

ID=16269851

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60191157A Expired - Lifetime JPH0651388B2 (en) 1985-08-30 1985-08-30 Matte film

Country Status (1)

Country Link
JP (1) JPH0651388B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03136891A (en) * 1989-07-06 1991-06-11 E I Du Pont De Nemours & Co Improvement element as non-impact printing receptor
KR100259117B1 (en) * 1996-11-22 2000-06-15 토마스 더블유. 버크맨 Stamping foil
JP2008073987A (en) * 2006-09-22 2008-04-03 Toyo Cloth Co Ltd Cloth for bankbooks, manufacturing process of cloth for bankbooks and bankbook

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60101083A (en) * 1983-11-08 1985-06-05 Dainippon Printing Co Ltd Thermal transfer sheet

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60101083A (en) * 1983-11-08 1985-06-05 Dainippon Printing Co Ltd Thermal transfer sheet

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03136891A (en) * 1989-07-06 1991-06-11 E I Du Pont De Nemours & Co Improvement element as non-impact printing receptor
KR100259117B1 (en) * 1996-11-22 2000-06-15 토마스 더블유. 버크맨 Stamping foil
JP2008073987A (en) * 2006-09-22 2008-04-03 Toyo Cloth Co Ltd Cloth for bankbooks, manufacturing process of cloth for bankbooks and bankbook

Also Published As

Publication number Publication date
JPH0651388B2 (en) 1994-07-06

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