JPS63268693A - Multitime use type thermal transfer recording medium - Google Patents
Multitime use type thermal transfer recording mediumInfo
- Publication number
- JPS63268693A JPS63268693A JP62103868A JP10386887A JPS63268693A JP S63268693 A JPS63268693 A JP S63268693A JP 62103868 A JP62103868 A JP 62103868A JP 10386887 A JP10386887 A JP 10386887A JP S63268693 A JPS63268693 A JP S63268693A
- Authority
- JP
- Japan
- Prior art keywords
- receptor
- recording medium
- porous structure
- thermal transfer
- resin
- 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
- 238000012546 transfer Methods 0.000 title claims abstract description 33
- 238000010438 heat treatment Methods 0.000 claims abstract description 8
- 229920005989 resin Polymers 0.000 claims description 43
- 239000011347 resin Substances 0.000 claims description 43
- 239000004840 adhesive resin Substances 0.000 claims description 15
- 229920006223 adhesive resin Polymers 0.000 claims description 15
- 230000001070 adhesive effect Effects 0.000 claims description 6
- 238000007639 printing Methods 0.000 abstract description 18
- 239000011148 porous material Substances 0.000 abstract description 6
- 230000002093 peripheral effect Effects 0.000 abstract 1
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 21
- 239000002904 solvent Substances 0.000 description 13
- 238000000034 method Methods 0.000 description 11
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 238000001035 drying Methods 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 239000000123 paper Substances 0.000 description 7
- 239000005038 ethylene vinyl acetate Substances 0.000 description 6
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 6
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 5
- 239000000853 adhesive Substances 0.000 description 5
- 239000004200 microcrystalline wax Substances 0.000 description 5
- 235000019808 microcrystalline wax Nutrition 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000000049 pigment Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- UHGGERUQGSJHKR-VCDGYCQFSA-N (2r,3r,4r,5s)-hexane-1,2,3,4,5,6-hexol;octadecanoic acid Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.CCCCCCCCCCCCCCCCCC(O)=O UHGGERUQGSJHKR-VCDGYCQFSA-N 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 229920006267 polyester film Polymers 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- ROGIWVXWXZRRMZ-UHFFFAOYSA-N 2-methylbuta-1,3-diene;styrene Chemical compound CC(=C)C=C.C=CC1=CC=CC=C1 ROGIWVXWXZRRMZ-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 3
- 229920006026 co-polymeric resin Polymers 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 239000011259 mixed solution Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 229920003048 styrene butadiene rubber Polymers 0.000 description 3
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical group CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 2
- 239000001856 Ethyl cellulose Substances 0.000 description 2
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 229920002301 cellulose acetate Polymers 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229920001249 ethyl cellulose Polymers 0.000 description 2
- 235000019325 ethyl cellulose Nutrition 0.000 description 2
- 239000012943 hotmelt Substances 0.000 description 2
- 229920002589 poly(vinylethylene) polymer Polymers 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000001055 blue pigment Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000000635 electron micrograph Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000011086 glassine Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000001878 scanning electron micrograph Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 238000010023 transfer printing Methods 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
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
- B41M5/382—Contact thermal transfer or sublimation processes
- B41M5/38278—Contact thermal transfer or sublimation processes using ink-containing structures, e.g. porous or microporous layers, alveoles or cellules
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、熱溶融転写方式に使用される多数回使用型の
熱転写記録媒体に関し、さらに詳しくは多孔質構造中に
加熱にて受容体に溶融転写する性質の着色インクが含有
されてなるインク保持層を存する多数回使用型熱転写記
録媒体に関す°る。Detailed Description of the Invention [Industrial Application Field] The present invention relates to a multi-use type thermal transfer recording medium used in a thermal melt transfer method, and more specifically, the present invention relates to a multi-use type thermal transfer recording medium used in a thermal melt transfer method. The present invention relates to a multi-use thermal transfer recording medium having an ink retaining layer containing a colored ink having a melt-transferable property.
この種の記録媒体としては、特開昭55−10’557
9号公報に開示されているものが知られているが、従来
の記録媒体を用いて印字したばあい、ゴーストとよばれ
る現象が発生していた。As a recording medium of this kind, Japanese Patent Application Laid-Open No. 55-10'557
A method disclosed in Japanese Patent No. 9 is known, but when printing using a conventional recording medium, a phenomenon called a ghost occurs.
当該ゴーストとは、第4図に示すように初回に印字した
印像パターン(たとえばWの文字)の輪郭が次回の印字
(たとえばIの文字)の際に薄く転写されてしまうとい
う現象であって、当該現象が生じると印像はとたんに不
鮮明になる。The ghost is a phenomenon in which the outline of the first printed image pattern (for example, the letter W) is lightly transferred during the next printing (for example, the letter I), as shown in Fig. 4. When this phenomenon occurs, the printed image immediately becomes unclear.
当該現象の原因は当初着色インクの感圧転写性によるも
のと考えられ、感圧転写性を低下するためにインクの融
点を上げたりすることが試みられたが、転写濃度の著し
い低下を招いて実用には至らなかった。The cause of this phenomenon was initially thought to be due to the pressure-sensitive transferability of the colored ink, and attempts were made to raise the melting point of the ink to reduce the pressure-sensitive transferability, but this resulted in a significant decrease in transfer density. It was not put into practical use.
本発明はこのような聞届をその原因を究明することによ
り、根本的に解決したものである。The present invention fundamentally solves this problem by investigating its cause.
本発明は、多孔質構造中に、加熱にて受容体に溶融転写
する性質の着色インクが包含されているインク保持層を
有する多数回使用型熱転写記録媒体において、前記多孔
質構造の表面が前記受容体に対し剥離可能に接着しうる
ようにされてなる多数回使用型熱転写記録媒体に関する
。The present invention provides a multi-use thermal transfer recording medium having an ink retaining layer in which a porous structure contains a colored ink that can be melted and transferred to a receptor by heating, wherein the surface of the porous structure is The present invention relates to a multi-use thermal transfer recording medium that can be releasably adhered to a receptor.
前記ゴースト現象を詳しく研究した結果、つぎのような
メカニズムで発生するものと推察される。第5図を参照
してこのメカニズムを説明する。As a result of detailed research on the ghost phenomenon, it is assumed that it occurs through the following mechanism. This mechanism will be explained with reference to FIG.
第5図において、al)は従来の多数回使用型熱転写記
録媒体であって、このものはベース02)上にインク保
持層03を設けたものであり、インク保持層には多孔質
構造04)の孔固中に熱溶融性の着色インク00が含宵
されてなるものである。第5図は、記録媒体01)を加
熱ヘッド■などでベース02)の裏面から加熱して着色
インク0■を受容体に溶融転写したのち、受容体を分離
したあとにおける記録媒体の状態を示すものである。In FIG. 5, al) is a conventional multi-use thermal transfer recording medium, which has an ink retaining layer 03 provided on a base 02), and the ink retaining layer has a porous structure 04). The hot-melt colored ink 00 is contained in the pores of the ink. Figure 5 shows the state of the recording medium after the recording medium 01) is heated from the back side of the base 02) using a heating head ■, etc. to melt and transfer the colored ink 0■ to the receiver, and then the receiver is separated. It is something.
第5図に示すように印字時の加熱箇所(A)と非加熱箇
所(B)との境のインク保持層(13]の表面にインク
(1ea)が残存していることが判明した。As shown in FIG. 5, it was found that ink (1ea) remained on the surface of the ink retaining layer (13) at the boundary between the heated area (A) and the non-heated area (B) during printing.
そしてこの表面に残存するインク(lea)が次回の印
字時に加熱ヘッドや通電ヘッドなどの圧接にて受容体に
転写されゴーストが発生するものと考えられるに至った
。It has come to be believed that the ink (lea) remaining on this surface is transferred to the receptor by pressure contact from a heating head, an energizing head, etc. during the next printing, causing ghosts.
そこで本発明においては、このようなインクの残存をな
くすために前記多孔質構造の表面を前記受容体に対し剥
離可能に接着しうるようにしたものである。Therefore, in the present invention, in order to eliminate such residual ink, the surface of the porous structure can be releasably adhered to the receptor.
つぎに図面に基づいて本発明の前記構成の作用を説明す
る。Next, the operation of the configuration of the present invention will be explained based on the drawings.
第1図は本発明の記録媒体の一実施例を示す概略部分断
面図である。第1図において、(1)は記録媒体であり
、このものはベース(z上にインク保持層(3)を設け
たものであり、インク保持層(3)は多孔質構造(4)
の孔(5)中に熱溶融性の着色インク(6)が含有され
てなるものである。そして、多孔質構造(4)の表面(
4a)は、少なくとも熱転写時に受容体に対し剥離可能
に接着しうるように構成されている。FIG. 1 is a schematic partial sectional view showing an embodiment of the recording medium of the present invention. In FIG. 1, (1) is a recording medium, which has an ink retaining layer (3) on a base (z), and the ink retaining layer (3) has a porous structure (4).
A hot-melt colored ink (6) is contained in the pores (5). Then, the surface of the porous structure (4) (
4a) is configured such that it can be releasably adhered to the receiver at least during thermal transfer.
前記構成によるときは、第2図に示すごとく、熱転写時
には加熱ヘッド■による加熱にて、印字箇所のインク保
持層(3)表面における多孔質構造(4)の孔(5)の
周辺は、当該多孔質構造(4)の表面(4a)が受容体
(21に接着することで閉止されてしまい、そのため加
熱によって溶融して前記孔(5)より溢れ出た着色イン
ク(6)は受容体+211の方向へのみ移動し、孔(5
)の周辺方向へ流れ出るようなことが生じなくなり、そ
の結果印字時の加熱箇所と非加熱箇所との境のインク保
持層(3)の表面に着色インク(6)が残存するような
ことがなくなった。When using the above configuration, as shown in FIG. 2, during thermal transfer, the area around the holes (5) of the porous structure (4) on the surface of the ink retaining layer (3) at the printing location is heated by the heating head (2). The surface (4a) of the porous structure (4) is closed by adhering to the receptor (21), and therefore the colored ink (6) that melts due to heating and overflows from the pores (5) is attached to the receptor +211. Move only in the direction of hole (5
), and as a result, the colored ink (6) does not remain on the surface of the ink retaining layer (3) at the boundary between the heated area and the non-heated area during printing. Ta.
さらに、多孔質構造表面は受容体に対して剥離可能に接
着しうるようにされているため、前記のごとき多孔質構
造の受容体に対する接着性は、インク保持層にいつまで
も保有されて接続性を有するものであり、したがって記
録媒体の同一箇所を繰り返し使用してもこのような機能
を繰り返し発揮してゴーストの発生が完全に防止される
。Furthermore, since the surface of the porous structure is designed to be releasably adhesive to the receptor, the adhesion of the porous structure to the receptor is retained in the ink retaining layer indefinitely and maintains connectivity. Therefore, even if the same location on the recording medium is used repeatedly, such a function is repeatedly exhibited and the occurrence of ghosts is completely prevented.
つぎに本発明の構成を具体的に説明する。Next, the configuration of the present invention will be specifically explained.
インク保持層は、ベース」―に設けられているのが一般
的である。当=亥ベースとしてはポリエステル、ポリア
ミド、ポリカーボネート、ポリイミドなどの合成樹脂か
らなる、厚さが1−15虜程度のフィルム、あるいはコ
ンデンサー紙、グラシン紙、インデア紙などの厚さが5
〜25珊程度の紙類、その他この種の記録媒体用として
従来から知られている各種のベース材料が使用可能であ
る。The ink retaining layer is generally provided on the base. The base material is a film made of synthetic resin such as polyester, polyamide, polycarbonate, polyimide, etc., with a thickness of about 1-15mm, or a film with a thickness of 5mm thick, such as condenser paper, glassine paper, India paper, etc.
It is possible to use various base materials conventionally known for use in this type of recording medium, such as paper with a weight of about 1.5 to 25 mm.
なお、当該ベースには、スティック現象を防止するため
に、背面(ヘッド接触面)に従来公知のスティック防止
層を設けたりするのもよい。Note that, in order to prevent the stick phenomenon, the base may be provided with a conventionally known stick prevention layer on the back surface (head contact surface).
また、当該ベースに導電性材料を混入して、通電転写方
式の発熱抵抗層としたり、静電気の除去作用を具備せし
めるようにしてもよい。さらに前記ベースの表面に多孔
質構造との結合力を高めるためのアンダーコート層を設
けるのも好ましい態様である。Further, a conductive material may be mixed into the base to form a heating resistance layer using an electric transfer method, or to provide a static electricity removal function. Furthermore, it is also a preferable embodiment to provide an undercoat layer on the surface of the base to enhance bonding strength with the porous structure.
つぎにインク保持層について説明する。Next, the ink retaining layer will be explained.
当該インク保持層は、多孔質構造とこれに包含された着
色インクとから構成されているものである。インク保持
層の厚さは、3〜20−程度が適当である。厚さが3虜
未満ではインク含有量が少なくなるため多数回転写性が
極端にわるくなり、一方2011mを超えると初期濃度
が低下する傾向にある。The ink retaining layer is composed of a porous structure and colored ink contained therein. The appropriate thickness of the ink retaining layer is about 3 to 20 mm. When the thickness is less than 3 mm, the ink content decreases, resulting in extremely poor multi-time transfer properties, while when it exceeds 2011 mm, the initial density tends to decrease.
前記多孔質構造としては、樹脂のみからなるもの、ある
いは多孔質粉体を樹脂にて結合したものなど、従来から
知られている多孔質構造がいずれも採用できる。As the porous structure, any conventionally known porous structure can be employed, such as one made only of resin or one in which porous powder is bonded with resin.
使用する樹脂は、印像形成時の加熱によっても分解や変
質を起さないような耐熱性を有するものがよく、また一
旦加熱された後でもベースから受容体に転写したり、層
分離を起さないようなベースとの接着性およびに内部凝
集力を有するもの°が好ましい。The resin used should be heat resistant so that it will not decompose or change in quality even when heated during image formation, and even once heated, it will not transfer from the base to the receptor or cause layer separation. Preferably, the material has adhesiveness to the base and internal cohesive strength such that it does not cause any damage.
当該樹脂としては、たとえばスチレン−イソプレン共重
合体樹脂、スチレン−ブタジェン共重合体樹脂、1.2
−ポリブタジェン樹脂、ポリエステル樹脂、ポリビニル
ブチラール樹脂、塩化ビニル−酢酸ビニル共重合体樹脂
、エチルセルロース樹脂、セルロースアセテート樹脂な
どの1種もしくはこれらの複数の混合物を使用すること
ができる。Examples of the resin include styrene-isoprene copolymer resin, styrene-butadiene copolymer resin, 1.2
- One or a mixture of polybutadiene resin, polyester resin, polyvinyl butyral resin, vinyl chloride-vinyl acetate copolymer resin, ethyl cellulose resin, cellulose acetate resin, etc., can be used.
また前記多孔質粉体としては、ケイソウ土、シリカなど
の平均粒径が0.3〜30−程度のものが使用できる。Further, as the porous powder, diatomaceous earth, silica, and the like having an average particle size of about 0.3 to 30 mm can be used.
当該多孔質構造の表面に受容体に対する接着性を帯有せ
しめる手段としては、■多孔質構造を構成する樹脂成分
として受容体に接着するようなものを使用したり、■当
該多孔質構造の表面に受容体に対して接着性を有する材
料をブルーミングさせる手段がある。As means for imparting adhesion to the receptor on the surface of the porous structure, there are two methods: 1. Using a resin component that adheres to the receptor as a resin component constituting the porous structure, 2. Another method is to bloom a material that is adhesive to the receptor.
多孔質構造の表面の受容体に対する接着性は少なくとも
熱転写時に備わっておればよく、常態時に接着性がある
か否かは問わない。It is sufficient that the surface of the porous structure has adhesion to the receptor at least during thermal transfer, and it does not matter whether or not it has adhesion under normal conditions.
前記■の手段に使用できる樹脂としては前記樹脂成分の
うち、スチレン−ブタジェン共重合体樹脂、1.2−ポ
リブタジェン樹脂、スチレン−イソプレン共重合体樹脂
などが適当に使用できる。Among the resin components mentioned above, styrene-butadiene copolymer resin, 1,2-polybutadiene resin, styrene-isoprene copolymer resin, etc. can be suitably used as the resin that can be used in the above-mentioned means (2).
前記■の手段に使用できる材料としては、多孔質構造を
主に構成する樹脂とは非相溶性であるが、該樹脂と分散
混合が可能な接着性樹脂を使用するのがよく、このもの
は主たる樹脂成分10重量部に対し0.2〜3.0重量
部程度配合するのが適当である。As a material that can be used for the above method (2), it is preferable to use an adhesive resin that is incompatible with the resin that mainly constitutes the porous structure, but can be dispersed and mixed with the resin. It is appropriate to add about 0.2 to 3.0 parts by weight to 10 parts by weight of the main resin component.
このブルーミング用の接着性樹脂としては、エチレン−
酢酸ビニル共重合体樹脂、エチレン−エチルアクリレー
ト共重合体樹脂、スチレン−ブタジェン共重合体樹脂、
スチレン−イソプレン共重合体樹脂、1.2−ポリブタ
ジェン樹脂、エチルセルロース樹脂、セルロースアセテ
ート樹脂、アクリル樹脂などの1種もしくはこれらの複
数の混合物を使用することができる。ただし樹脂成分の
接着性は受容体の表面の性質により変化する可能性があ
るので、受容体によってはこれ以外の樹脂を使用するこ
とも可能である。The adhesive resin for blooming is ethylene-
Vinyl acetate copolymer resin, ethylene-ethyl acrylate copolymer resin, styrene-butadiene copolymer resin,
One type of styrene-isoprene copolymer resin, 1,2-polybutadiene resin, ethyl cellulose resin, cellulose acetate resin, acrylic resin, or a mixture of a plurality of these resins can be used. However, since the adhesiveness of the resin component may vary depending on the surface properties of the receptor, other resins may be used depending on the receptor.
前記ブルーミングは、多孔質構造の主たる樹脂を溶解す
る揮発性溶剤の沸点より高い沸点を有しかつ主たる樹脂
を実質的に溶解しない溶剤に接着性樹脂を溶解し、乾燥
時に、まず主たる樹脂成分の溶剤を蒸発させ、ついで接
着性樹脂の溶剤を蒸発させて、当該接着性樹脂を表面に
浮き出させるようにするのが適当である。In the blooming process, adhesive resin is dissolved in a solvent that has a boiling point higher than that of a volatile solvent that dissolves the main resin of the porous structure and does not substantially dissolve the main resin, and when dried, the main resin component is first dissolved. It is appropriate to evaporate the solvent and then evaporate the solvent of the adhesive resin so that the adhesive resin stands out on the surface.
接着性樹脂を多孔質構造の表面にブルーミングさせる態
様において、多孔質構造の主たる樹脂と接着性樹脂との
好ましい組合せを第1表に示す。Table 1 shows preferred combinations of the main resin of the porous structure and the adhesive resin in an embodiment in which the adhesive resin is bloomed onto the surface of the porous structure.
前記ブルーミング用接着性樹脂としてエチレン−酢酸ビ
ニル共重合体は好ましいものであるが、とりわけ酢酸ビ
ニルの含有量が15〜50重量%、なかんづ<30〜4
0%重量のものが好ましい。Ethylene-vinyl acetate copolymer is preferable as the adhesive resin for blooming, especially when the content of vinyl acetate is 15 to 50% by weight and <30 to 4% by weight.
0% weight is preferred.
前記着色インクはそのベヒクルが多孔質構造を構成する
樹脂と実質的に非相溶のものである。The colored ink has a vehicle that is substantially incompatible with the resin constituting the porous structure.
前記着色インクを多孔質構造内に包含せしめる方法とし
ては、■当該着色インクと多孔質構造の樹脂成分とを適
宜の溶剤中に非相溶の状態で分散混合し、この分散混合
した塗剤をベースに塗布し乾燥する方法と、■多孔質粉
体に前記着色インクを含浸させたものと樹脂成分とを適
宜の溶剤に分散混合してえた塗剤をベースに塗布し乾燥
する方法と、■着色インクを粉砕してえた同形粉体と樹
脂成分の溶剤溶液(溶剤として着色インクを溶解しない
ものを用いる)とを該固形粉体がそれ程微細化しない程
度に軽く混合してえた塗剤をベースに塗布し乾燥する方
法などを用いるのが適当である。The method for incorporating the colored ink into the porous structure is as follows: (1) Dispersing and mixing the colored ink and the resin component of the porous structure in an incompatible state in an appropriate solvent, and using the dispersion-mixed coating material. (1) A method in which a coating obtained by dispersing and mixing a porous powder impregnated with the colored ink and a resin component in an appropriate solvent is applied on the base and dried; A base coating material obtained by lightly mixing a uniform powder obtained by crushing colored ink with a solvent solution of a resin component (use a solvent that does not dissolve the colored ink) to the extent that the solid powder does not become too fine. It is appropriate to use a method such as coating and drying.
前記着色インクは従来の熱溶融転写インクと同様なもの
でよく、天然もしくは合成のワックスや低融点の熱可塑
性樹脂を主体とするベヒクルに染料、顔料などの着色剤
を分散混合したもので、常温で固体もしくはゲル状のも
のである。The colored ink may be similar to conventional heat-melting transfer ink, and is a mixture of colorants such as dyes and pigments dispersed in a vehicle mainly composed of natural or synthetic wax or low-melting thermoplastic resin. It is solid or gel-like.
このようにしてえたインク保持層の表面の接着力は熱転
写用紙に対し、180’剥離試験での平均剥離強さが1
0〜50g[’程度のものが適当である。The adhesive strength of the surface of the ink retaining layer thus obtained was determined by an average peel strength of 1 in a 180' peel test against thermal transfer paper.
Approximately 0 to 50 g[' is appropriate.
前記180’剥離試験の測定条件はつぎのとおりである
。The measurement conditions for the 180' peel test are as follows.
剥離試験機:新車科学■製表面性測定機11EIDON
=14型
受容体:熱転写用紙(十條製紙■製TRW−7)試験片
;8.35+a■巾の試験リボンを前記受容体ニ重ね合
せ、サーマルヘッドを用い
0.4vの印字エネルギーにてリボンの中全体にわたっ
てベタ印字して作製し
た。Peeling tester: Shinsha Kagaku ■ surface property measuring machine 11EIDON
= 14-type receptor: thermal transfer paper (TRW-7 manufactured by Jujo Paper Industries) test piece; A test ribbon of 8.35+a width was placed on the receptor, and the ribbon was printed using a thermal head with a printing energy of 0.4V. It was produced by solid printing all over the inside.
前記剥離強さがlOg!’より小さいと、ゴースト防止
効果が劣る傾向にあり、一方50gfより大きいと印字
後記録媒体と受容体との分離がスムーズにいかず、記録
媒体の送りが阻害されるなどの不具合が生じる傾向にあ
る。The peel strength is lOg! If it is smaller than 50gf, the ghost prevention effect tends to be poor, while if it is larger than 50gf, the separation between the recording medium and the receptor after printing will not be smooth, and problems such as hindering the feeding of the recording medium will tend to occur. be.
なお、前記剥離強さの上限値は受容体の表面状態やリボ
ンの引張強さや、引き剥がし力の大小などにより左右さ
れるものであり、したがってこれ以上の値であっても支
障なく使用しうるばあいは多々あるものである。Note that the upper limit of the peel strength mentioned above depends on the surface condition of the receptor, the tensile strength of the ribbon, the magnitude of the peeling force, etc. Therefore, even if the value is higher than this, it can be used without any problem. There are many cases.
つぎに実施例をあげて本発明の記録媒体を説明する。Next, the recording medium of the present invention will be described with reference to Examples.
実施例1
接着性樹脂としてのエチレン−酢酸ビニル共重合体(酢
酸ビニル含有量35重量%)1部(重量部、以下同様)
をトルエン9部に溶解し、一方多孔質構造の主体樹脂と
しての塩化ビニル−酢酸ビニル共重合体(酢酸ビニル含
有量17重量%)9部をメチルエチルケトン45部に溶
解した。Example 1 Ethylene-vinyl acetate copolymer (vinyl acetate content 35% by weight) as adhesive resin 1 part (parts by weight, the same applies hereinafter)
was dissolved in 9 parts of toluene, and on the other hand, 9 parts of vinyl chloride-vinyl acetate copolymer (vinyl acetate content: 17% by weight) as the main resin having a porous structure was dissolved in 45 parts of methyl ethyl ketone.
前記2種の溶液を混合し、これに着色インク成分として
のマイクロクリスタンワックス7部、ソルビットステア
レート1部および着色顔料5部を溶解分散した。The above two types of solutions were mixed, and 7 parts of microcrystalline wax, 1 part of sorbitol stearate, and 5 parts of colored pigment as colored ink components were dissolved and dispersed therein.
えられた混合液を厚さ6JIMのポリエステルフィルム
上に乾燥後厚さが8廓となるように塗布し、まず!10
℃で乾燥してメチルエチルケトンを蒸発させ、ついで1
00℃で乾燥して残りの溶剤を蒸発させて、多孔質構造
中にむ色インクが含有され、かつ多孔質構造の表面にエ
チレン−酢酸ビニル共重合体がブルーミングしたインク
保持層を有する記録媒体をえた。After drying, apply the resulting mixed solution onto a polyester film with a thickness of 6JIM so that the thickness becomes 8JM, and then! 10
evaporate the methyl ethyl ketone by drying at 1
A recording medium obtained by drying at 00°C to evaporate the remaining solvent and having an ink-retaining layer containing a blue ink in a porous structure and blooming ethylene-vinyl acetate copolymer on the surface of the porous structure. I got it.
実施例2〜3
実施例1におけるエチレン−酢酸ビニル共重合体にかえ
てつぎのエチレン−酢酸ビニル共重合体を用いたほかは
実施例1と同様にして記録媒体を作製した。Examples 2 to 3 Recording media were produced in the same manner as in Example 1, except that the following ethylene-vinyl acetate copolymer was used instead of the ethylene-vinyl acetate copolymer in Example 1.
実施例2:酢酸ビニル含有量33重は%実施例3:酢酸
ビニル含有量32重量%実施例4
接着性樹脂としてのエチレン−エチルアクリレート共重
合体(エチルアクリレート含有量35重量%)1部をト
ルエン9部に溶解し、一方多孔質構造の主体樹脂として
のポリビニルブチラール樹脂(ブチラール基含有量68
モル%)7部をメチルエチルケトン40部に溶解した。Example 2: Vinyl acetate content 33% by weightExample 3: Vinyl acetate content 32% by weightExample 4 1 part of ethylene-ethyl acrylate copolymer (ethyl acrylate content 35% by weight) as adhesive resin Polyvinyl butyral resin (butyral group content: 68
(mol%) was dissolved in 40 parts of methyl ethyl ketone.
前記2種の溶液を混合し、これに着色インク成分として
のマイクロクリスタンワックス7部、ソルビットステア
レート1部および着色顔料5部を溶解分散した。The above two types of solutions were mixed, and 7 parts of microcrystalline wax, 1 part of sorbitol stearate, and 5 parts of colored pigment as colored ink components were dissolved and dispersed therein.
えられた混合液を厚さ6部mのポリエステルフィルム上
に乾燥後厚さが8虜となるように塗布し、まず80℃で
乾燥してメチルエチルケトンを蒸発させ、ついで100
℃で乾燥して残りの溶剤を蒸発させて、多孔質構造中に
着色インクが含有され、かつ多孔質構造の表面にエチレ
ン−エチルアクリレート共重合体がブルーミングしたイ
ンク保持層を有する記録媒体をえた。The resulting mixed solution was applied onto a polyester film with a thickness of 6 parts m so that the thickness after drying would be 8 mm, first dried at 80°C to evaporate the methyl ethyl ketone, and then
The remaining solvent was evaporated by drying at ℃ to obtain a recording medium having an ink retaining layer containing colored ink in a porous structure and blooming ethylene-ethyl acrylate copolymer on the surface of the porous structure. .
実施例5
接着性樹脂としてのスチレン−イソプレン共重合体(ス
チレン/イソプレン−21/ 79 (ffI ffI
比))1部をトルエン9部に溶解し、一方多孔質構造の
主体樹脂としてのポリビニルブチラール樹脂(ブチラー
ル基含有率約88モル%)9部をメチルエチルケトン4
5部に溶解した。Example 5 Styrene-isoprene copolymer (styrene/isoprene-21/79 (ffI ffI
(ratio)) was dissolved in 9 parts of toluene, and on the other hand, 9 parts of polyvinyl butyral resin (butyral group content: about 88 mol%) as the main resin with a porous structure was dissolved in 4 parts of methyl ethyl ketone.
It was dissolved in 5 parts.
前記2種の溶液を混合し、これに着色インク成分として
のマイクロクリスタンワックス7部、ソルビットステア
レート1部および着色顔料5部を溶解分散した。The above two solutions were mixed, and 7 parts of microcrystalline wax, 1 part of sorbitol stearate, and 5 parts of a color pigment as colored ink components were dissolved and dispersed therein.
えられた混合液を厚さ4.−のコンデンサー紙上に乾燥
後厚さが5廓となるように塗布し、まず60℃で乾燥し
てメチルエチルケトンを蒸発させ、ついで100℃で乾
燥して残りの溶剤を蒸発させて、多孔質構造中に着色イ
ンクが含有され、かつ多孔質構造の表面にスチレン−イ
ソプレン共重合体がブルーミングしたインク保持層を有
する記録媒体をえた。Thicken the resulting mixture to a thickness of 4. - After drying, the film was coated on condenser paper to a thickness of 5 layers, first dried at 60°C to evaporate the methyl ethyl ketone, and then dried at 100°C to evaporate the remaining solvent, forming a porous structure. A recording medium was obtained which had an ink retaining layer containing a colored ink and a styrene-isoprene copolymer blooming on the surface of a porous structure.
実施例6
多孔質構造の主体樹脂かつ接着性樹脂としての1.2−
ポリブタジェン(破断強度100kg/cd)9部をト
ルエン45部に溶解し、これに着色インク成分としての
マイクロクリスタリンワックス10部および着色顔料5
部を溶解分散した。Example 6 1.2- as main resin with porous structure and adhesive resin
9 parts of polybutadiene (breaking strength 100 kg/cd) was dissolved in 45 parts of toluene, and 10 parts of microcrystalline wax as a colored ink component and 5 parts of a colored pigment were added to the solution.
part was dissolved and dispersed.
えられた混合液を厚さ6虜のポリエステルフィルム上に
乾燥後厚さが10廓となるように塗布し、90℃で乾燥
して溶剤を蒸発させて、多孔質構造中に着色インクが含
有され、多孔質構造全体が接着性樹脂から構成されてい
るインク保持層を有する記録媒体をえた。The resulting mixed solution was applied onto a polyester film with a thickness of 6 mm to a thickness of 10 mm after drying, and dried at 90°C to evaporate the solvent, resulting in the colored ink being contained in the porous structure. A recording medium having an ink retaining layer whose entire porous structure is composed of an adhesive resin was obtained.
比較例
実施例1で用いたと同じ塩化ビニル−酢酸ビニル共重合
体9部をメチルエチルケトン45部に溶解し、これに6
色インク成分としてのマイクロクリスタリンワックス7
部、ソルビットステアレート1部および青色顔料5部を
溶解分散した。Comparative Example 9 parts of the same vinyl chloride-vinyl acetate copolymer used in Example 1 was dissolved in 45 parts of methyl ethyl ketone, and 6 parts of
Microcrystalline wax as a color ink component 7
1 part of sorbitol stearate and 5 parts of blue pigment were dissolved and dispersed.
えられた混合液を厚さ6烏のポリエステルフィルム上に
乾燥後厚さが8廁−となるように塗布し、80℃で乾燥
して溶剤を蒸発させて、多孔質構造中に着色インクが含
有されたインク保持層を有する記録媒体をえた。The resulting mixture was applied onto a polyester film with a thickness of 6 cm to a dry thickness of 8 cm, dried at 80°C to evaporate the solvent, and the colored ink was deposited in the porous structure. A recording medium having an ink retaining layer contained therein was obtained.
えられた各記録媒体について、インク保持層表面の受容
体に対する接着力(180’剥離強さ)を測定した。For each recording medium obtained, the adhesive force (180' peel strength) of the surface of the ink retaining layer to the receptor was measured.
また前記各記録媒体を使用し、感熱プリンター(シャー
プ■製wO−55型)で印字を行ない、多数回転写性お
よびゴーストの発生の6無を調べた。Further, using each of the above-mentioned recording media, printing was carried out with a thermal printer (WO-55 model manufactured by Sharp ■), and multi-time transferability and occurrence of ghost were examined.
これらの結果を第2表に示す1゜第2表における多数回
転写性は、記録媒体の同一箇所で繰り返し印字を行ない
、印字濃度が0.5に低下するまでの印字回数で示した
。These results are shown in Table 2. 1. The multiple transferability in Table 2 is expressed as the number of times printing is performed until the print density decreases to 0.5 when printing is repeatedly performed on the same location on the recording medium.
さらに前記各記録媒体を使用し、前記感熱プリンターで
印字を1回おこなったのち、各記録媒体の表面状態を走
査型電子顕微鏡で写真にとり、観察した。第3図は実施
例1の、記録媒体についての電子顕微鏡写J:4(倍率
1000倍)に基づくスケッチ図である。第3図におい
て、上半分は未使用の部分であり、下半分は使用した部
分である。第3図に示されるごとく使用部分には毛羽立
ち様のものが見られる。これは熱転写時に多孔質構造の
表面に接着していた受容体を転写後引き剥がしたために
多孔質構造の表面の接着性樹脂が毛羽立ったものである
。Further, each of the recording media was used to print once using the thermal printer, and then the surface condition of each recording medium was photographed and observed using a scanning electron microscope. FIG. 3 is a sketch diagram based on an electron micrograph J:4 (magnification: 1000 times) of the recording medium in Example 1. In FIG. 3, the upper half is an unused portion, and the lower half is a used portion. As shown in Figure 3, there is some fuzz-like material in the used area. This is because the adhesive resin on the surface of the porous structure became fluffy because the receptor adhered to the surface of the porous structure during thermal transfer was peeled off after the transfer.
実施例2〜6の記録媒体についても使用部分に同様な毛
羽立ちが認められたが、比較例の記録媒体においては多
孔質構造の表面が受容体に対して接着性でないため、使
用部分にこのよう毛羽立ちが認められなかった。Similar fuzziness was observed in the used areas of the recording media of Examples 2 to 6, but since the surface of the porous structure of the recording media of Comparative Examples was not adhesive to the receptor, such fuzziness was observed in the used areas. No fluff was observed.
第 2 表
〔発明の効果〕
多数回使用型熱転写記録媒体を用いて印字する際に、同
一箇所で繰り返し印字してもゴーストが発生しないので
、繰り返し多数回印字を行なっても初回のばあいと同程
度の鮮明な印像がえられる。Table 2 [Effects of the Invention] When printing using a multi-use thermal transfer recording medium, ghosts do not occur even if printing is repeated at the same location, so even if printing is performed many times, it is not the case for the first time. A similarly clear impression can be obtained.
第1図は本発明の多数回使用型熱転写記録媒体の一実施
例を示す概略部分断面図、第2図は該記録媒体を用いて
熱転写印字する際の状態を示す説明図、第3図は該記録
′媒体の使用後の表面の走査型電子顕微鏡写真(倍率1
000倍)に基づくスケッチ図、第4図は従来の多数回
使用型熱転写記録媒体を使用するばあいに発生するゴー
スト現象を示す説明図、第5図はゴーストの発生メカニ
ズムを示す概略説明図である。
(図面の主要符号)
(3):インク保持層。
(4):多孔質構造
(6)二着色インク
21:受容体FIG. 1 is a schematic partial sectional view showing an embodiment of the multi-use thermal transfer recording medium of the present invention, FIG. 2 is an explanatory view showing the state when thermal transfer printing is performed using the recording medium, and FIG. Scanning electron micrograph of the surface of the recording medium after use (magnification: 1
Figure 4 is an explanatory diagram showing the ghost phenomenon that occurs when using a conventional multi-use thermal transfer recording medium, and Figure 5 is a schematic diagram showing the ghost generation mechanism. be. (Main symbols in the drawings) (3): Ink retaining layer. (4): Porous structure (6) Two-color ink 21: Receptor
Claims (1)
質の着色インクが包含されているインク保持層を有する
多数回使用型熱転写記録媒体において、前記多孔質構造
の表面が前記受容体に対し剥離可能に接着しうるように
されてなる多数回使用型熱転写記録媒体。 2 前記多孔質構造が、主成分の樹脂と、これに非相溶
で前記受容体に対して接着性を有する接着性樹脂とから
なり、かつ当該接着性樹脂にて前記多孔質構造の表面が
覆われてなる特許請求の範囲第1項記載の多数回使用型
熱転写記録媒体。 3 前記受容体への接着性が熱転写時の加熱にて発現さ
れるものである特許請求の範囲第1項または第2項記載
の多数回使用型熱転写記録媒体。[Scope of Claims] 1. A multi-use thermal transfer recording medium having an ink retaining layer in which a porous structure contains a colored ink that can be melted and transferred to a receptor upon heating. A multi-use thermal transfer recording medium, the surface of which is adapted to releasably adhere to the receptor. 2. The porous structure is composed of a resin as a main component and an adhesive resin that is incompatible with the resin and has adhesive properties to the receptor, and the surface of the porous structure is covered with the adhesive resin. A multi-use thermal transfer recording medium according to claim 1, which is covered. 3. The multi-use thermal transfer recording medium according to claim 1 or 2, wherein the adhesion to the receptor is developed by heating during thermal transfer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62103868A JPS63268693A (en) | 1987-04-27 | 1987-04-27 | Multitime use type thermal transfer recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62103868A JPS63268693A (en) | 1987-04-27 | 1987-04-27 | Multitime use type thermal transfer recording medium |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63268693A true JPS63268693A (en) | 1988-11-07 |
Family
ID=14365417
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62103868A Pending JPS63268693A (en) | 1987-04-27 | 1987-04-27 | Multitime use type thermal transfer recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63268693A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0372585A2 (en) * | 1988-12-09 | 1990-06-13 | Seiko Epson Corporation | Thermal transfer recording medium |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6273994A (en) * | 1985-09-27 | 1987-04-04 | Fuji Kagakushi Kogyo Co Ltd | Multiple-time use type thermal transfer recording medium |
JPS6277987A (en) * | 1985-10-02 | 1987-04-10 | Mitsubishi Chem Ind Ltd | Thermal transfer recording medium |
-
1987
- 1987-04-27 JP JP62103868A patent/JPS63268693A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6273994A (en) * | 1985-09-27 | 1987-04-04 | Fuji Kagakushi Kogyo Co Ltd | Multiple-time use type thermal transfer recording medium |
JPS6277987A (en) * | 1985-10-02 | 1987-04-10 | Mitsubishi Chem Ind Ltd | Thermal transfer recording medium |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0372585A2 (en) * | 1988-12-09 | 1990-06-13 | Seiko Epson Corporation | Thermal transfer recording medium |
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