JPS623987A - Ink sheet for thermal transfer recording - Google Patents
Ink sheet for thermal transfer recordingInfo
- Publication number
- JPS623987A JPS623987A JP60142831A JP14283185A JPS623987A JP S623987 A JPS623987 A JP S623987A JP 60142831 A JP60142831 A JP 60142831A JP 14283185 A JP14283185 A JP 14283185A JP S623987 A JPS623987 A JP S623987A
- Authority
- JP
- Japan
- Prior art keywords
- ink sheet
- thermal transfer
- peroxide
- transfer recording
- recording ink
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/40—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography
- B41M5/42—Intermediate, backcoat, or covering layers
- B41M5/44—Intermediate, backcoat, or covering layers characterised by the macromolecular compounds
- B41M5/443—Silicon-containing polymers, e.g. silicones, siloxanes
Landscapes
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は感熱転写配録インクシートに関1ノ、更に詳し
くは転写型の感熱記録装置に用いられる記録媒体の一部
を形成するインクシートに関する。Detailed Description of the Invention (Field of Industrial Application) The present invention relates to a thermal transfer recording ink sheet, and more particularly to an ink sheet forming a part of a recording medium used in a transfer type thermal recording device. Regarding.
(従来の技術〕
近来、情報機器の鵡及、進展は[1覚ましいしのがあり
特にパーソナル]ンビ]−タ、Aフィス]ンビコーク、
ワードプ+:+ 1=ツナ−の酋及に伴ない、これらに
搭載されるプリンターが急増1ノでいる。(Prior Art) In recent years, the spread and progress of information devices has been [1] particularly important, especially personal computers, electronic devices, electronic devices, electronic devices, electronic devices, etc.
Wordpress+:+1=With the popularity of tuna, the number of printers installed on these devices has increased rapidly.
この様な費用の中で、小型、軽量、低価格で信頼性の高
い熱転写プリンターは、インクシー1へに所定の熱量を
印加し、インクを記録紙に移行さ1することにより記録
を行うものである。Despite these costs, thermal transfer printers, which are small, lightweight, low-priced, and highly reliable, perform recording by applying a predetermined amount of heat to the ink sheet 1 and transferring the ink to the recording paper 1. be.
この熱転写に関してはいくつかの6式があり、代表的な
ものには熱量印加にサーマルヘッドを用い、シート上に
顔料を含有したワックス層を設()、リーマルヘッド熱
量印加部を被転写紙に溶融転写する方法、同じ、り胃華
竹染料をバインダー中に含有【ノ、号−マルヘッド熱品
印加で昇華、拡散転写する方法等があり、また加熱方式
どじでインクシー1−を介した通電加熱によるタイプの
ものなどがある。There are several types of thermal transfer, and the typical one uses a thermal head to apply heat, a wax layer containing pigment is placed on the sheet (), and the thermal head heat application part is connected to the transfer paper. There is a method of melting and transferring the same, a method of sublimation and diffusion transfer by applying a heated product to a multi-head, and a method of sublimation and diffusion transfer by applying a heated product to the same head, and a method of applying electricity through an ink sheet using a heating method. There are also types that use heating.
これらはいずれもより高感度、即ら高速印字等が求めら
れ、おのずと比較的融点の低い材料がインク層として使
用されなければならない。然るに、このインクシートは
プリンターへの装着の都合からカートリッジ化さ′れ、
ロール状゛或いはシートが積層された形態を取らざるを
得す、この状態では比較的融点の低い材料がインク層と
し・て使用されるため、巻圧或いは自重によ゛りいわゆ
るブ「1ツキングを生起し、これによりインク層の移行
剥離、あるいは側面しみ出しによる一体化又は、インク
シー十、リボン端部の脱落が・起るという難点がある。All of these require higher sensitivity, ie, high-speed printing, and naturally a material with a relatively low melting point must be used as the ink layer. However, this ink sheet was made into a cartridge for convenience in installing it in the printer.
In this state, a material with a relatively low melting point is used as the ink layer, so the so-called "one book" type is formed due to the rolling pressure or its own weight. This causes problems such as migration and peeling of the ink layer, integration due to lateral seepage, or falling off of the ink sheet and ribbon ends.
−
〔発明が解決しようどする問題点〕
本発明が解決しようとする問題点は従来のインクシート
の上記難点、即ちインクシートを[1−ル状またはシー
トが積層された形態を採る場合に生ずる所謂ブ1コッキ
シグに基ずく難点を解決しようとする□ことである。
゛
(問題点を解決するための手段)
上記問題点は、インクシートの熱量゛が印加゛される側
□に、特定の末端ビニル基を有するポリシロキ勺ンの過
酸化物による架W6v!!化物から成る層を好ましくは
その厚み0.02−1”で形成することににり解決され
る。即ら本発明は熱量が印加される側に、下記一般式
%式%)
〈但しAは−c l−1= c、 +−+4、Meはメ
チル基、pl+(JLフェニル基を表わす)
で表される冬−2〜1.0’00,000の末端ビニル
基6一
を有するボリシロキ4ノーンを過酸化物にて架橋硬化し
て成る硬化物から(7る層を形成1)′で成る感熱転写
記録インクシートに係るものである。- [Problems to be Solved by the Invention] The problems to be solved by the present invention are the above-mentioned difficulties of conventional ink sheets, that is, problems that occur when the ink sheet is in the form of a single roll or a stack of sheets. It is an attempt to solve the problems based on so-called B1 coxing.
(Means for solving the problem) The above problem is caused by the use of a peroxide bridge W6v of polysiloxane having a specific terminal vinyl group on the side of the ink sheet to which the heat is applied. ! This problem is solved by forming a layer consisting of a compound with a thickness of preferably 0.02-1". That is, the present invention provides the following general formula (%) on the side to which the amount of heat is applied (where A is -c l-1=c, +-+4, Me is a methyl group, pl+ (represents JL phenyl group) -2~1.0'00,000 polysiloxy4 with a terminal vinyl group 61 This invention relates to a heat-sensitive transfer recording ink sheet consisting of a cured product obtained by cross-linking and curing Norn with a peroxide (forming seven layers 1)'.
元来この種インクシー1−の背面処理とし−C1その熱
m印加時に生ずる動点を改善するための処理がある。即
ちインクシー1−基材の軟化によるスティッキング現象
を耐熱竹材料にて被覆することにJ:り排除あるいは基
材の潰り竹改良にて排除lノJ、うとする処理であり、
これ等については、たとえば特公昭58−13359、
特開昭55−146790、特開昭56−155794
、特開昭57−129789、特開昭58−171’1
92、特開昭58−187396等があり、シリコン系
化合物を使用するものもある。しかしながらこれ等番よ
いずれも熱量印加配録11¥の瞬時の現象についての処
理であり、熱量印加時に生ずる瞬間的な基材の軟化ある
いは滑り竹を改善するための処理であって、これ等処理
に於ては、基材の熱的な、或いは基材の摩擦面にお(J
る特性が大きく影響をあたえるものである。Originally, there was a treatment for the back side of this type of InkC1-C1 to improve the moving point that occurs when heat m is applied to it. In other words, Ink Sea 1 is a treatment that attempts to eliminate the sticking phenomenon caused by softening of the base material by covering it with a heat-resistant bamboo material or by improving the bamboo by crushing the base material.
Regarding these, for example, Special Publication No. 58-13359,
JP-A-55-146790, JP-A-56-155794
, JP-A-57-129789, JP-A-58-171'1
92, JP-A-58-187396, etc., and some use silicon-based compounds. However, all of these treatments are treatments for the instantaneous phenomenon of heat application, and are treatments to improve the instantaneous softening or slipping of the base material that occurs when heat is applied. In this case, the heat of the base material or the friction surface of the base material (J
The characteristics of
これに対し本発明で解決しようとするブロッキング防止
は長期間経峙後の剥離性が問題となるものであって、上
記従来の熱m印加時の瞬間的な現象に対応する処理とは
本質的に全く異なるものであって、これ等従来の処理に
於いて効果があるものが、そのまま本発明のブロッキン
グ防1Fに使用した場合に効果があるか否かということ
は全く不明のことである。On the other hand, the blocking prevention that the present invention seeks to solve involves the problem of releasability after long-term use, and the above-mentioned conventional treatment that deals with instantaneous phenomena when applying heat m is essentially It is completely unknown whether or not these methods, which are effective in conventional processing, will be effective when used as they are in the anti-blocking method 1F of the present invention.
本発明に用いられる一般式
%式%)
(但しAは一〇 H= CI−1,、Meはメチル基、
Phはフェニル基を表わす)
で表されるAL−2〜1.000,000の末端ビニル
基を有するポリシロキサン(以下これ等を総称してビニ
ル変性ポリシロキサンという)としては、例えば、チッ
ソ■製のたとへば、p3437(At: 2−3)〜
449..5 (τ: 1..000,00(1)
、PS 463、PS 464735、PS 737
.・6、p 3 、762、PS765、PS 76
−7.5、p3782、PS785、l”’8787等
を挙°げることか出来る。General formula used in the present invention (% formula %) (where A is 10 H= CI-1, Me is a methyl group,
(Ph represents a phenyl group) AL-2 to 1.000,000 polysiloxanes having terminal vinyl groups (hereinafter collectively referred to as vinyl-modified polysiloxanes) include those manufactured by Chisso ■. Notobe, p3437 (At: 2-3) ~
449. .. 5 (τ: 1..000,00(1)
, PS 463, PS 464735, PS 737
..・6, p 3 , 762, PS 765, PS 76
-7.5, p3782, PS785, l'''8787, etc.
本発明において使用される過酸化物としては。Peroxides used in the present invention include:
3級ブチルパーAクトエートや3級ブチルパービバレー
トなどのパー1ステル、ビス−(4−3級ブチルシクロ
ヘキシル
−トの如き過炭酸ニスデル、ベンゾイルパーオキ−〇−
シトの如きジアシルバーオキシド、ジ−3級ブチルパー
オキシドやジクミルパーオキシドの如きジアルキルパー
オキシド、シクロヘキサノンパーA4ニシド、メチルエ
チルケトンパー
ンヒドロパーAキシドなどのヒドロパーオキシドがあげ
られ、好ましくは、ベンゾイルパーオキサイドの如きジ
アシルパーオキシド系である。Peresters such as tertiary butyl peractoate and tertiary butyl perbivalate, bis-(nisdel percarbonate such as 4-tert-butyl cyclohexylate, diasilver oxide such as benzoyl peroxide, di- Examples include dialkyl peroxides such as tertiary butyl peroxide and dicumyl peroxide, hydroperoxides such as cyclohexanone per A4 oxide, and methyl ethyl ketone per A4 oxide, preferably diacyl peroxides such as benzoyl peroxide. .
また、本発明においては他のポリマーまた(よオリゴマ
ー系化合物を併用することも出来、この際の他のポリマ
ーとしては、たとえばエチレン−酢酸ビニル、Tチレン
ーアクリルなどのエチレン系共重合体、ポリスチレン、
スチレン−ブタジェン共重合体、ゴム類、セルロース誘
導体、ブチラール、ポリビニルアルコール
ネート、ポリ塩化ビニル、エポキシメラミン、ポリエス
テル、ポリエーテルポリウレタン、及び上記のオリゴマ
ー状化合物等が例示出来、これ等は通常0.5.80重
量%の割合で併用される。In addition, in the present invention, other polymers or oligomeric compounds can also be used in combination, such as ethylene copolymers such as ethylene-vinyl acetate, T-tyrene-acrylic, and polystyrene. ,
Examples include styrene-butadiene copolymers, rubbers, cellulose derivatives, butyral, polyvinyl alcoholate, polyvinyl chloride, epoxymelamine, polyesters, polyether polyurethanes, and the above oligomeric compounds, and these are usually 0.5 Used in combination at a ratio of .80% by weight.
更に本発明に於いては無機質添加剤を使用することを妨
げない。この際の無機質添加剤は例えば熱伝導性の低下
を避けるため、又通電加熱等の場合はその導電性を妨げ
ない等の目的で使用され、好ましい具体例として金属粉
たとえば銀、銅、鉄。Furthermore, the present invention does not preclude the use of inorganic additives. The inorganic additives used in this case are used, for example, in order to avoid a decrease in thermal conductivity, or in the case of electrical heating, for the purpose of not interfering with the conductivity. Preferred specific examples include metal powders such as silver, copper, and iron.
アルミニウム等、金属酸化物粉末ICとえばアルミナ、
チタン白、ガラス等、無機塩粉末たとえば炭酸カルシウ
ム、硫酸ナトリウム、クレイ類等をあげることが出来、
その使用量は通常ビニル変性ポリシロキサンと他の添加
物との総量に対して1〇−80重石部程度である。Metal oxide powder IC such as alumina, etc.
Examples include titanium white, glass, etc., inorganic salt powders such as calcium carbonate, sodium sulfate, clays, etc.
The amount used is usually about 10-80 parts by weight based on the total amount of vinyl-modified polysiloxane and other additives.
上記一般式で表されるビニル変性ポリシロキリンの硬化
物層をインクシー1−の熱量が印加される側に形成する
に際しては、該化合物及び過酸化物をそのまま或いは適
宜な不活性溶剤で希釈lノでインクシートの所定個所に
適宜な手段たとえば塗布手段等により形成せしめ次いで
所定の処理により架橋硬化せしめる。この際の不活+1
1溶剤として(よ作業性の点にり沸点50−150°C
のノブのが好ましく、具体的にはたとえば、トルニ[−
ン、キシレン、ヘキリン、酢酸エチル、酢酸ブチル、ア
セ]・ン、メチルエチルケトン、メチルイソブチルケト
ン等が例示出来る。本発明のビニル変性ボリシローヤサ
ンの硬化物層を形成せしめる順序と1ノでは、基材にイ
ンク層を設【Jだ後でも良く、また予め基材にビニル変
性ボリシロキ1[ンの硬化物層を8941.その後イン
ク層を設けても良い。塗布厚み番、1硬化物の厚みとし
て0.02=1 好ましくは0.05−0.5 の
範囲であり、0.02・ 以下では均一な効果がl!I
l持できず、また 1 以上ではインクシートの感電が
低下し望ましくない。When forming a cured layer of vinyl-modified polysiloquiline represented by the above general formula on the heat-applied side of Inksy 1-, the compound and peroxide may be used as is or diluted with an appropriate inert solvent. It is formed on a predetermined portion of an ink sheet by an appropriate means such as a coating means, and then cross-linked and cured by a predetermined treatment. Inactive +1 at this time
1 as a solvent (boiling point 50-150°C for better workability)
Preferably, the knob is, for example, Torni [-
Examples include xylene, hexylene, ethyl acetate, butyl acetate, acetate, methyl ethyl ketone, and methyl isobutyl ketone. The order of forming the cured layer of vinyl-modified polysiloxane according to the present invention is as follows: In step 1, an ink layer may be formed on the base material. .. An ink layer may then be provided. Coating thickness number, 1 The thickness of the cured product is in the range of 0.02 = 1, preferably 0.05-0.5, and below 0.02, the uniform effect is l! I
If it is more than 1, the electric shock of the ink sheet will decrease, which is not desirable.
本処理硬化物層は溶剤使用の場合はこれを揮散させ、イ
ンタ層或いはり材が狽されない範囲、通常60〜100
℃の加熱で1ワられる。If a solvent is used for this treatment, the cured product layer must be volatilized to prevent the interlayer or beam material from being weakened, usually 60 to 100%.
When heated to ℃, it becomes 1 wa.
本発明のビニル変性ポリジロー1−リンの硬化物層を形
成せしめるインクシートとしては、特に限定せれず従来
から使用されて来た各種のタイプのものがいずれも使用
出来る。なかでも特に溶融転写タイプのものが本発明の
効果が特に顕著に発揮される。これ等インクシートは上
記でのべた通り特に限定されるものではないが、本発明
に於いて好ましく使用される溶融転写タイプのものを例
にとって説明すると、2−12μ厚み程度のポリエステ
ルフィルム基材上に、60−100℃程度の溶融点を有
するパラフィンワックスやエステルワックスと色材どか
ら必要に応じ柔軟剤や熱伝導性向上剤たる充填剤と共に
調製したインク層を2−2074程度の厚みで設けたも
のを例示出来る。The ink sheet on which the cured layer of vinyl-modified polygyro-1-phosphorus of the present invention is formed is not particularly limited, and any of the various types conventionally used can be used. Among these, the effects of the present invention are particularly noticeable in the melt-transfer type. These ink sheets are not particularly limited as mentioned above, but to explain the melt transfer type that is preferably used in the present invention as an example, it can be applied to a polyester film base material with a thickness of about 2 to 12 μm. Then, an ink layer prepared from paraffin wax or ester wax having a melting point of about 60-100°C and a coloring material, along with a filler as a softener and a thermal conductivity improver as necessary, is provided to a thickness of about 2-2074°C. I can give examples.
色材としても広い範囲で各種のものが使用出来、たとえ
ば染料便覧(丸善株式会ネ1発行、1970年)に於い
て顔別表に記載されている顔料やカーボンブラックの如
き顔料、直接染11、分散染料、塩基性染料、酸性染料
等の各種染料が使用出来る。A wide variety of coloring materials can be used; for example, pigments listed in the face table in the Dye Handbook (published by Maruzen Co., Ltd., 1970), pigments such as carbon black, direct dyeing 11, Various dyes such as disperse dyes, basic dyes, and acid dyes can be used.
特にイエローの色材どしてはり1]ルフエニルアゾ基を
有するもの、マゼンタの色材としてはナフ]・−ルアゾ
基を有するもの、またシアンの色材どしてはフタロシア
ニン構造を有するものが好ましい。In particular, yellow coloring materials are preferably those having a 1] ruphenylazo group, magenta coloring materials are preferably having a naph]--luazo group, and cyan coloring materials are preferably having a phthalocyanine structure.
柔軟剤としては従来から使用されて来たものが使■出来
、たとえばエチレン−酢酸ビニル、エチレン−アクリル
などのエチレン系共重合体、ポリスチレン、スチレン−
ブタジェン共重合体、ゴム類、セルロース誘導体、ブチ
ラール、ポリビニルアルコール、ポリアミド、ポリカー
ボネート、ポリ塩化ビニル、エポキシメラミン、ポリエ
ステル、ポリエーテルポリウレタン及び上記のオリゴマ
ー状化合物等の容易に熱溶融し得る物質、または潤滑油
などが挙げられる。As softeners, conventionally used ones can be used, such as ethylene-based copolymers such as ethylene-vinyl acetate, ethylene-acrylic, polystyrene, and styrene-based softeners.
Easily heat-meltable substances such as butadiene copolymers, rubbers, cellulose derivatives, butyral, polyvinyl alcohol, polyamides, polycarbonates, polyvinyl chloride, epoxymelamine, polyesters, polyether polyurethanes, and the above oligomeric compounds, or lubricants. Examples include oil.
充填剤としても従来から使用されて来たものが使用出来
、金属粉たとえば銀、銅、鉄、アルミニウム等、金属酸
化物粉末たとえばアルミナ、チタン白、ガラス等、無機
塩粉末たとえば炭酸カルシウム、硫酸ナトリウl\、ク
レイ等を具体例として挙げることが出来る。Fillers that have traditionally been used can be used, such as metal powders such as silver, copper, iron, aluminum, etc., metal oxide powders such as alumina, titanium white, glass, etc., and inorganic salt powders such as calcium carbonate and sodium sulfate. Specific examples include l\, clay, and the like.
以下に実施例を示して本発明を具体的に説明する6
゛
実施例1゜
パラフィンワックス#155(軟化点69℃)100重
石部及びカーボンブラックMA−8.,20重吊部を1
00℃にて溶融混合分散させて黒色のホットメルトイン
クを作成した。The present invention will be specifically explained with reference to Examples 6 below.
゛Example 1゛Paraffin wax #155 (softening point 69°C) 100 weights and carbon black MA-8. , 20 heavy lifting parts in 1
A black hot melt ink was prepared by melting and mixing and dispersing at 00°C.
このインクをJIII mr下厚み6〃のポリエステル
フィルム上に4/Pの厚みでホッ]−メルト]−ティン
グした(比較資料)。εのインクシートを表裏交Hに5
枚重ねとし、2枚のガラス板にはさみ、50090分銅
加重下にて50℃の恒温槽にて加温した。This ink was hot-melted on a JIII mr polyester film with a thickness of 6 mm to a thickness of 4/P (comparative material). 5 Ink sheets of ε are crossed on the front and back H.
The sheets were stacked, sandwiched between two glass plates, and heated in a constant temperature bath at 50° C. under a weight of 50,090.
−六本発明のインクシートとして上記インクシートの裏
面にチッソ(株)製ビニル変竹ボリシ[1キサンPS
437(1,= 2−3)の1%1ヘルエン溶液に、ベ
ンゾイルパーオキサイドをビニル変11Iポリシロキサ
ン100重吊部に対して5重量部添加し、これを塗布し
、加熱して硬化せしめた。この厚みは0.2 であっ
た(本発明品)、本発明のインタシートを上記と同様に
表裏交互に5枚重ねどし、2枚のガラス板にはさみ、5
00jJの分銅加重下にで上記比較資料と同時に50℃
の恒温槽にて加温した。24時間加温後両資利を取りだ
したところ、比較質11はブロッキングを生起しており
、剥離しようとしたところランダムにインクの裏面えの
転写が認められた。−六本発明のビニル変性ボリシロキ
+タンの硬化物層を裏面に有するインクシートはその剥
離等においても何ら劣化は認められなかった。-6 As an ink sheet of the present invention, on the back side of the above ink sheet, a vinyl modified bamboo borish made by Chisso Co., Ltd. [1Kisan PS
5 parts by weight of benzoyl peroxide was added to a 1% 1 heluene solution of 437 (1, = 2-3) per 100 parts of vinyl modified 11I polysiloxane, and this was applied and cured by heating. . This thickness was 0.2 (product of the present invention). Five sheets of the Intasheet of the present invention were stacked alternately on the front and back sides in the same manner as above, and sandwiched between two glass plates.
Under a weight load of 00jJ, at the same time as the above comparative data, 50℃
It was heated in a constant temperature bath. When both materials were taken out after heating for 24 hours, it was found that Comparative Material No. 11 had caused blocking, and when attempts were made to peel it off, random transfer of the ink to the back side was observed. -6 No deterioration was observed in the ink sheet having the vinyl-modified polysiloxy+tan cured product layer of the present invention on the back surface even when it was peeled off.
実施例2゜
酸価ワックスNPS−9125(軟化点63℃)100
重石部及びβ−ナフトール・アゾ系顔料Permane
nt Carmine F B B O2,7重石
部を100℃にて溶融混合分散させてマゼンタ色系のホ
ットメルトインクを作成した。Example 2 Acid value wax NPS-9125 (softening point 63°C) 100
Weight part and β-naphthol azo pigment Permane
A magenta hot melt ink was prepared by melting and dispersing nt Carmine F B B O2, heptadite at 100°C.
このインクを加温下・厚み6I′のポリ1ステルフイル
ム上に4.IAの厚みでホットメルトコーティングした
(比較資料)。このインクシートを実施例1と同様に表
裏交互に5枚重ねとし、2枚のガラス板にはさみ、50
0gの分銅加重下にて50℃の恒温槽にて加温した。−
六本発明のインクシートとして上記インクシートの裏面
にチッソ(株)製ビニル変性ポリシ[lキサンPS46
301%トルエン溶液に実施例1と同様にベンゾイルパ
ーオキサイド5部を配合し、塗布後加熱して硬化せしめ
た。4. Apply this ink on a 6I' thick polyester film under heating. Hot-melt coating was applied to the thickness of IA (comparison material). As in Example 1, 5 sheets of this ink sheet were stacked alternately on the front and back sides, sandwiched between two glass plates, and
It was heated in a constant temperature bath at 50° C. under a weight of 0 g. −
6. As an ink sheet of the present invention, a vinyl modified polyurethane [lxane PS46 manufactured by Chisso Co., Ltd.] is coated on the back side of the above ink sheet.
5 parts of benzoyl peroxide was added to a 301% toluene solution in the same manner as in Example 1, and after coating, it was heated and cured.
この硬化物の厚み&j、0.2μであった。本発明のイ
ンクシートを上記と同様に表裏交互に5枚重ねとし、2
枚のガラス板にはさみ、500gの分銅加重下にて上記
比較資料と同時に50℃の恒温槽にて加湿した。24時
間加温後両資利を取りだしたところ、IL較資判はブロ
ッキングを生起しており、剥離しようとしたところラン
ダムにインクの裏面への転写が認められた。−六本発明
のビニル変性ポリシロキサンの硬化物層を裏面に有する
インクシートはその剥離等においても何ら劣化は認めら
れなかった。The thickness of this cured product was 0.2μ. Five ink sheets of the present invention were stacked alternately on the front and back sides in the same manner as above, and 2
It was placed between two glass plates and humidified in a constant temperature bath at 50° C. at the same time as the above comparative material under a weight of 500 g. When both sheets were taken out after heating for 24 hours, blocking had occurred on the IL reference sheet, and when an attempt was made to peel it off, ink was randomly transferred to the back surface. -6 No deterioration was observed in the ink sheet having the vinyl-modified polysiloxane cured layer of the present invention on the back surface even when it was peeled off.
上記実施例からも判る様に、本発明インクシートは極め
てすぐれた耐ブロッキング性を示す。As can be seen from the above examples, the ink sheet of the present invention exhibits extremely excellent blocking resistance.
(以上)(that's all)
Claims (8)
hはフェニル基を表わす) で表されるm=2〜1,000,000の末端ビニル基
を有するポリシロキサンを過酸化物にて架橋硬化して成
る硬化物から成る層を形成して成る感熱転写記録インク
シート。(1) On the side where the amount of heat is applied, the following general formula ▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ ▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ ▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ (q = 2-20 %) (However, A is -CH=1-CH_2, Me is a methyl group, P
h represents a phenyl group) Polysiloxane having a terminal vinyl group with m = 2 to 1,000,000 is crosslinked and cured with a peroxide to form a layer of a cured product. Thermal transfer recording ink sheet.
物から成る層の厚みが0.02〜1μである特許請求の
範囲第1項記載の感熱転写記録インクシート。(2) The thermal transfer recording ink sheet according to claim 1, wherein the layer made of the cured polysiloxane having a terminal vinyl group has a thickness of 0.02 to 1 μm.
請求の範囲第1または2項に記載の感熱転写記録インク
シート。(3) The thermal transfer recording ink sheet according to claim 1 or 2, wherein the ink sheet is of a melt transfer type.
ポリエステルフィルム基材上に60−100℃の溶融点
を有するパラフィンワックスまたはエステルワックスと
色材とから調製されたものである特許請求の範囲第3項
に記載の感熱転写記録インクシート。(4) The claim that the melt transfer type ink sheet is prepared from a paraffin wax or ester wax having a melting point of 60-100°C and a coloring material on a 2-12μ polyester film base material. The thermal transfer recording ink sheet according to item 3.
特許請求の範囲第1項記載の感熱転写記録インクシート
。(5) The thermal transfer recording ink sheet according to claim 1, wherein the peroxide is a diacyl peroxide type.
許請求の範囲第1項記載の感熱転写記録インクシート。(6) The thermal transfer recording ink sheet according to claim 1, wherein the peroxide is a diacyl peroxide type.
請求の範囲第1項記載の感熱転写記録インクシート。(7) The thermal transfer recording ink sheet according to claim 1, wherein the peroxide is a hydroperoxide type.
ゾ基を有するイエロー色材、ナフトールアゾ基をするマ
ゼンタ色材、またはフタロシアニン構造を有するシアン
色材である特許請求の範囲第1乃至4項のいずれかに記
載の感熱転写記録インクシート。(8) Claims 1 to 4, wherein the coloring material contained in the ink sheet is a yellow coloring material having a chlorphenylazo group, a magenta coloring material having a naphtholazo group, or a cyan coloring material having a phthalocyanine structure. The thermal transfer recording ink sheet according to any one of the above.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60142831A JPS623987A (en) | 1985-06-28 | 1985-06-28 | Ink sheet for thermal transfer recording |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60142831A JPS623987A (en) | 1985-06-28 | 1985-06-28 | Ink sheet for thermal transfer recording |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS623987A true JPS623987A (en) | 1987-01-09 |
Family
ID=15324629
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60142831A Pending JPS623987A (en) | 1985-06-28 | 1985-06-28 | Ink sheet for thermal transfer recording |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS623987A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4807341A (en) * | 1987-10-13 | 1989-02-28 | Eastman Kodak Company | Toner fusing roll covered with crosslinked elastomeric siloxane copolymer containing diphenylsiloxane recurring units and method of preparation |
| US5001012A (en) * | 1989-01-23 | 1991-03-19 | Minnesota Mining And Manufacturing Company | Thermal transfer donor element |
-
1985
- 1985-06-28 JP JP60142831A patent/JPS623987A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4807341A (en) * | 1987-10-13 | 1989-02-28 | Eastman Kodak Company | Toner fusing roll covered with crosslinked elastomeric siloxane copolymer containing diphenylsiloxane recurring units and method of preparation |
| US5001012A (en) * | 1989-01-23 | 1991-03-19 | Minnesota Mining And Manufacturing Company | Thermal transfer donor element |
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