JPH11105442A - Many times thermal transfer recording medium to be used - Google Patents
Many times thermal transfer recording medium to be usedInfo
- Publication number
- JPH11105442A JPH11105442A JP9291523A JP29152397A JPH11105442A JP H11105442 A JPH11105442 A JP H11105442A JP 9291523 A JP9291523 A JP 9291523A JP 29152397 A JP29152397 A JP 29152397A JP H11105442 A JPH11105442 A JP H11105442A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- fine particles
- heat
- recording medium
- thermal transfer
- 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
- 229920005989 resin Polymers 0.000 claims abstract description 57
- 239000011347 resin Substances 0.000 claims abstract description 57
- 239000010419 fine particle Substances 0.000 claims abstract description 33
- 230000003578 releasing effect Effects 0.000 claims abstract description 8
- 229920002050 silicone resin Polymers 0.000 claims abstract description 5
- 239000011248 coating agent Substances 0.000 claims description 16
- 238000000576 coating method Methods 0.000 claims description 16
- 239000002245 particle Substances 0.000 claims description 8
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 4
- 229910052731 fluorine Inorganic materials 0.000 claims description 4
- 239000011737 fluorine Substances 0.000 claims description 4
- 238000007639 printing Methods 0.000 abstract description 14
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 abstract description 2
- HGAZMNJKRQFZKS-UHFFFAOYSA-N chloroethene;ethenyl acetate Chemical compound ClC=C.CC(=O)OC=C HGAZMNJKRQFZKS-UHFFFAOYSA-N 0.000 abstract description 2
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 abstract 2
- 229920001296 polysiloxane Polymers 0.000 abstract 2
- 239000010410 layer Substances 0.000 description 36
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 12
- 239000012943 hotmelt Substances 0.000 description 12
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 10
- 239000007788 liquid Substances 0.000 description 10
- 229910052710 silicon Inorganic materials 0.000 description 10
- 239000010703 silicon Substances 0.000 description 10
- 239000001993 wax Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 7
- DTCCVIYSGXONHU-CJHDCQNGSA-N (z)-2-(2-phenylethenyl)but-2-enedioic acid Chemical compound OC(=O)\C=C(C(O)=O)\C=CC1=CC=CC=C1 DTCCVIYSGXONHU-CJHDCQNGSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 230000032798 delamination Effects 0.000 description 3
- 239000012188 paraffin wax Substances 0.000 description 3
- -1 polypropylene Polymers 0.000 description 3
- 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
- 229920000877 Melamine resin Polymers 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 2
- 239000004203 carnauba wax Substances 0.000 description 2
- 235000013869 carnauba wax Nutrition 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 229920001249 ethyl cellulose Polymers 0.000 description 2
- 235000019325 ethyl cellulose Nutrition 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001721 polyimide Polymers 0.000 description 2
- DHKHKXVYLBGOIT-UHFFFAOYSA-N 1,1-Diethoxyethane Chemical compound CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- QLZJUIZVJLSNDD-UHFFFAOYSA-N 2-(2-methylidenebutanoyloxy)ethyl 2-methylidenebutanoate Chemical compound CCC(=C)C(=O)OCCOC(=O)C(=C)CC QLZJUIZVJLSNDD-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 239000011354 acetal resin Substances 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 229910021486 amorphous silicon dioxide Inorganic materials 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 239000004204 candelilla wax Substances 0.000 description 1
- 235000013868 candelilla wax Nutrition 0.000 description 1
- 229940073532 candelilla wax Drugs 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000012461 cellulose resin Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000005042 ethylene-ethyl acrylate Substances 0.000 description 1
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000003779 heat-resistant material Substances 0.000 description 1
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 1
- 238000007757 hot melt coating Methods 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 239000012170 montan wax Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 235000019809 paraffin wax Nutrition 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 239000009719 polyimide resin Substances 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 230000008542 thermal sensitivity Effects 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Landscapes
- Thermal Transfer Or Thermal Recording In General (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は熱転写記録媒体に関し、
詳しくは多数回熱転写記録媒体に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a thermal transfer recording medium,
More specifically, the present invention relates to a thermal transfer recording medium for multiple times.
【0002】[0002]
【従来の技術】ファクシミリ、各種プリンター等の記録
装置において熱転写記録方法は、記録装置の小型化、低
価格化が著しく普及しており、それに用いられる熱転写
記録媒体の需要も増加の一途をたどっている。しかし従
来の熱転写記録媒体は、支持体上に熱溶融性インク層を
1層または2層設けるのが一般的であり、これらの熱転写
記録媒体はサーマルヘッドから加熱、加圧された箇所の
熱溶融性インクは、すべて受像紙側へ転写される。2. Description of the Related Art In thermal transfer recording methods for recording apparatuses such as facsimile machines and various printers, the miniaturization and cost reduction of recording apparatuses have become extremely widespread, and the demand for thermal transfer recording media used therein has been steadily increasing. I have. However, the conventional thermal transfer recording medium has a heat-fusible ink layer on a support.
Generally, one or two layers are provided. In these thermal transfer recording media, the heat-fusible ink at the location heated and pressed by the thermal head is all transferred to the image receiving paper side.
【0003】従ってこれらの熱転写記録媒体は、同一箇
所で多数回使用することは困難であり、熱転写記録媒体
の使用量が増えランニングコストの点で問題があった。
また昨今の環境問題、廃棄物の点においても問題とな
り、同一箇所で繰り返し使用可能な即ち多数回熱転写記
録媒体が求められている。[0003] Therefore, it is difficult to use these thermal transfer recording media many times in the same place, and the amount of use of the thermal transfer recording media increases, and there is a problem in running cost.
In addition, there has been a problem in recent environmental problems and wastes, and a thermal transfer recording medium that can be used repeatedly at the same place, that is, a large number of times, has been demanded.
【0004】そこで現在までに種々の多数回熱転写記録
媒体が提案されておりその幾つかをあげると、(1)支
持体上に複数の接着層および熱溶融性インク層を設け、
少しずつ熱溶融性インクを転写させる方法、(2)支持
体上に熱溶融性インクおよび非熱軟化性の多孔質形成樹
脂からなるインク層を設け、熱溶融性インクを少しずつ
しみ出させる方法、(3)支持体上に熱溶融性インクお
よびそれとは非相溶性の過冷却成分からなるインク層を
設け、インク層の凝集破壊による層間剥離により少しず
つインクを転写させる方法、等が提案されている。Therefore, various thermal transfer recording media of various types have been proposed so far. Some of them are as follows: (1) A plurality of adhesive layers and a hot-melt ink layer are provided on a support;
A method of transferring the heat-meltable ink little by little, (2) a method of providing an ink layer made of a heat-meltable ink and a non-thermosoftening porous forming resin on a support and exuding the hot-melt ink little by little And (3) a method of providing an ink layer composed of a heat-meltable ink and a supercooled component incompatible with the ink on a support, and transferring the ink little by little by delamination due to cohesive failure of the ink layer. ing.
【0005】しかしながら前記(1)の熱転写記録媒体
は、印字回数ごとにインクの転写が一定ではない欠点が
ある。前記(2)の熱転写記録媒体は、印字回数ごとに
インクのしみ出し量が減少し濃度低下が激しいという欠
点がある。前記(3)の熱転写記録媒体は、印字環境温
度によりインク層の凝集破壊が不安定である。また、層
間剥離によりインクを転写させる方法であるため層間剥
離により、インクのけばだちによるゴーストが発生する
欠点がある。[0005] However, the thermal transfer recording medium of the above (1) has a disadvantage that the transfer of ink is not constant with the number of times of printing. The thermal transfer recording medium of the above (2) has a drawback that the amount of oozing out of the ink decreases with the number of times of printing and the density decreases sharply. In the thermal transfer recording medium (3), the cohesive failure of the ink layer is unstable depending on the printing environment temperature. In addition, since the method of transferring ink by delamination is used, there is a disadvantage that ghost is generated due to the flash of ink due to delamination.
【0006】これらの欠点を解消するために、特開平5
−246156号公報、特開平6−64340号公報に
開示されているように、支持体上に熱溶融性インク層を
設け、さらにその上層に熱溶融性微粒子を含む転写制御
層を設け、熱溶融性インクの流出量を制御する方法が提
案されている。しかしこの方法による熱転写記録媒体
は、転写制御層中に含まれている熱溶融性微粒子が初回
の印字で受像紙に転写するため、2回目以後の印字にお
いて形成された画像に転写ムラが発生する欠点がある。In order to eliminate these disadvantages, Japanese Patent Laid-Open No.
As disclosed in JP-A-246156 and JP-A-6-64340, a heat-meltable ink layer is provided on a support, and a transfer control layer containing heat-meltable fine particles is further provided thereon to form a heat-meltable ink layer. There has been proposed a method of controlling the outflow amount of the volatile ink. However, in the thermal transfer recording medium according to this method, since the heat-fusible fine particles contained in the transfer control layer are transferred to the image receiving paper in the first printing, transfer unevenness occurs in an image formed in the second and subsequent printings. There are drawbacks.
【0007】[0007]
【発明が解決しようとする課題】本発明は従来技術の欠
点を解消し、多数回使用しても均一な高印字濃度および
高印字品質を得ることが可能な多数回熱転写記録媒体を
提供することを目的とする。また多数回使用によるイン
クのけばだちによる地汚れやゴーストを防止した多数回
熱転写記録媒体を提供することを目的とする。SUMMARY OF THE INVENTION The present invention has been made to overcome the disadvantages of the prior art and to provide a multiple-time thermal transfer recording medium capable of obtaining uniform high print density and high print quality even when used multiple times. With the goal. It is another object of the present invention to provide a thermal transfer recording medium which is prevented from being soiled or ghosted due to ink flapping due to multiple use.
【0008】[0008]
【課題を解決するための手段】本発明者は前記課題を解
決し、多数回使用しても高印字濃度および高印字品質が
得られる多数回熱転写記録媒体を得るために鋭意研究を
行なった結果、熱溶融性インク層の上層に、熱溶融性イ
ンクの転写を制御しうる非熱軟化性または高軟化点を有
する被膜形成樹脂成分と離型性樹脂成分および非熱溶融
性微粒子からなる転写制御層を設け、転写制御層が熱溶
融性インクおよび受像紙に対して離型作用を有すること
により、課題の解決を成し得ることを見出した。Means for Solving the Problems The inventors of the present invention have solved the above-mentioned problems, and have conducted intensive studies in order to obtain a thermal transfer recording medium which can obtain high print density and high print quality even when used many times. A transfer control comprising a non-thermosoftening or high softening point film-forming resin component, a release resin component and non-thermofusible fine particles, which can control the transfer of the hot-melt ink to the upper layer of the hot-melt ink layer. It has been found that the problem can be solved by providing a layer and the transfer control layer having a releasing effect on the heat-fusible ink and the image receiving paper.
【0009】以下に本発明を更に詳しく説明する。転写
制御層は転写制御層形成樹脂に含有された非熱溶融性微
粒子と、サーマルヘッドからの熱による熱溶融性インク
の熱膨張、サーマルヘッドとプラテン間の圧力と毛細管
現象によりほぼ均一に孔が開けられこの孔から熱溶融性
インクがしみ出され、かつ非熱溶融性微粒子を有するこ
とにより、転写制御層形成樹脂と受像紙が完全に密着す
ることなく印字濃度的に十分なインク量が溶融状態でし
み出る。しみ出た熱溶融状態のインクは、転写制御層が
離型作用を有しているため、すべてが受像紙側へ冷却固
化し高濃度高品質印字が得られる。またこれらの作用に
より、転写時熱溶融性インクのけばだちが生じず多数回
使用時の感圧転写による、地汚れやゴーストが発生しな
い。Hereinafter, the present invention will be described in more detail. The transfer control layer has non-thermal fusible fine particles contained in the resin for forming the transfer control layer, the thermal expansion of the heat fusible ink due to the heat from the thermal head, the pressure between the thermal head and the platen, and a substantially uniform hole due to the capillary phenomenon. The hot-melt ink exudes from this hole and has non-heat-meltable fine particles, so that the transfer control layer forming resin and the image receiving paper do not completely adhere to each other, so that a sufficient amount of ink in terms of print density can be melted. Exudes in a state. All of the exuded ink in the heat-melted state is cooled and solidified on the image receiving paper side because the transfer control layer has a releasing effect, and high-density high-quality printing is obtained. In addition, due to these effects, the fusing of the heat-fusible ink does not occur at the time of transfer, and background dirt and ghost due to pressure-sensitive transfer at the time of multiple use do not occur.
【0010】転写制御層の熱溶融性インクの制御につい
ては、非熱溶融性微粒子を有することにより熱溶融性イ
ンクがしみ出た際、転写制御層を介して支持体側の熱溶
融性インクと転写制御層形成樹脂との接触面積が、しみ
出た熱溶融性インクと転写制御層形成樹脂とのそれより
大きいため、熱溶融性インクが冷却固化されても転写制
御層形成樹脂は支持体側の熱溶融性インク側に残り、全
転写することなく多数回制御しつづける。Regarding the control of the heat-fusible ink in the transfer control layer, when the heat-fusible ink exudes due to the presence of the non-heat-fusible fine particles, the transfer control layer transfers the heat-fusible ink to the heat-fusible ink on the support side via the transfer control layer. Since the contact area with the control layer forming resin is larger than that of the exuded heat-fusible ink and the transfer control layer forming resin, even if the heat-fusible ink is cooled and solidified, the transfer control layer forming resin does not have heat on the support side. It remains on the fusible ink side and continues to be controlled many times without transferring all.
【0011】本発明に用いられる被膜形成樹脂成分とし
ては、非熱軟化性または高軟化点を有する樹脂が用いら
れ、具体的には軟化点が130℃以上の塩化ビニル−酢
酸ビニル樹脂、塩化ビニル樹脂、ポリビニルブチラール
樹脂、ポリビニルアセタール樹脂、ポリエステル樹脂、
アクリル樹脂、スチレンマレイン酸樹脂、セルロース樹
脂等の1種または複数が用いられる。As the film-forming resin component used in the present invention, a resin having a non-thermal softening property or a high softening point is used. Specifically, a vinyl chloride-vinyl acetate resin having a softening point of 130 ° C. or more, vinyl chloride, Resin, polyvinyl butyral resin, polyvinyl acetal resin, polyester resin,
One or more of acrylic resin, styrene-maleic acid resin, cellulose resin and the like are used.
【0012】また前述の被膜形成樹脂成分には、熱溶融
性インクおよび受像紙に対して離型作用を有することを
目的として、シリコン樹脂、シリコン変性樹脂、フッ素
系樹脂等の離型性樹脂成分の1種または複数が用いられ
る。In addition, the above-mentioned film-forming resin component has a releasing resin component such as a silicone resin, a silicon-modified resin, a fluorine-based resin, etc., for the purpose of having a releasing effect on the hot-melt ink and the image receiving paper. One or more of these are used.
【0013】本発明に用いられる非熱溶融性微粒子とし
ては、熱や圧力等の要因により軟化および分解すること
のない微粒子が用いられ、その具体例としてはシリコン
微粒子、フッ素系微粒子、メラミン系微粒子、二酸化珪
素等の1種または複数を混合して用いる。As the non-thermofusible fine particles used in the present invention, fine particles which do not soften or decompose due to factors such as heat and pressure are used. Specific examples thereof include silicon fine particles, fluorine fine particles, and melamine fine particles. , Silicon dioxide or the like, or a mixture thereof.
【0014】前述の非熱溶融性微粒子の平均粒子径とし
ては、0.5μm〜5μmのものが使用される。これよ
り小さいと転写制御層形成樹脂と受像紙が完全に密着し
てしまい濃度的に不十分なインク量しかしみ出さず印字
が濃度不足になり、逆にこれより大きいと転写制御層形
成樹脂からしみ出した熱溶融性インクが受像紙に接触す
ることなく冷却固化してしまい転写不良となる。これら
より高濃度、高品質印字を得るためには、平均粒子径が
2μm〜4μmの微粒子を用いることが好ましい。The average particle diameter of the non-heat-meltable fine particles is 0.5 μm to 5 μm. If it is smaller than this, the transfer control layer forming resin and the image receiving paper are completely adhered to each other, and the density of the ink is insufficient. The exuded hot-melt ink is solidified by cooling without contacting the image receiving paper, resulting in poor transfer. In order to obtain higher density and higher quality printing, it is preferable to use fine particles having an average particle diameter of 2 μm to 4 μm.
【0015】転写制御層中の全樹脂と非熱溶融性微粒子
の重量比としては、転写制御層形成樹脂:非熱溶融性微
粒子=75:25〜25:75が好ましい。非熱溶融性
微粒子が、25%以下では転写制御層形成樹脂に十分な
孔が開かず濃度不足や転写不良が生じ、逆に75%以上
では非熱溶融性微粒子に対して転写制御層形成樹脂のバ
インダー力が弱くなり、熱溶融性インクと共に受像紙側
へ転写してしまい2回目以後の印字で全転写を起こして
しまう。The weight ratio of the entire resin in the transfer control layer to the non-heat-meltable fine particles is preferably transfer resin-forming resin: non-heat-meltable fine particles = 75: 25 to 25:75. When the amount of the non-heat-fusible fine particles is 25% or less, sufficient holes are not opened in the resin for forming the transfer control layer, resulting in insufficient concentration or poor transfer. Is weakened and is transferred to the image receiving paper side together with the hot-melt ink, and the entire transfer occurs in the second and subsequent printings.
【0016】転写制御層のコーティング量としては、
0.05g/平方メートル〜1.0g/平方メートルで
あることが好ましい。0.05g/平方メートル以下で
は転写制御しきれず全転写してしまい、1.0g/8平
方メートル以上では印字濃度に低下が見られる。さらに
好ましくは、熱溶融性インク層と転写制御層のトータル
コーティング量としては5g/平方メートル〜12g/
平方メートルである。The coating amount of the transfer control layer is as follows:
It is preferably from 0.05 g / m 2 to 1.0 g / m 2. At 0.05 g / m 2 or less, the transfer cannot be completely controlled, and the entire image is transferred. At 1.0 g / 8 m 2 or more, the print density is reduced. More preferably, the total coating amount of the heat-fusible ink layer and the transfer control layer is 5 g / m 2 to 12 g / m 2.
Square meters.
【0017】本発明に使用される支持体は既に公知であ
る耐熱性を有する材料、例えばポリエステル、ポリプロ
ピレン、ポリカーボネート、ナイロン、ポリイミド、ポ
リスチレン等のプラスティックフィルム、パラフィン
紙、コンデンサー紙等が使用される。支持体の厚さは熱
感度、強度の点から、3μm〜10μm程度であること
が好ましい。また支持体上の背面には耐熱保護層とし
て、シリコン樹脂、フッ素樹脂、フェノール樹脂、エポ
キシ樹脂、メラミン樹脂、ポリイミド樹脂等のノンステ
ィック層を設け、支持体の耐熱性を向上させることがで
きる。The support used in the present invention is a known heat-resistant material, for example, a plastic film such as polyester, polypropylene, polycarbonate, nylon, polyimide, or polystyrene, paraffin paper, or condenser paper. The thickness of the support is preferably about 3 μm to 10 μm from the viewpoint of thermal sensitivity and strength. In addition, a non-stick layer such as a silicone resin, a fluorine resin, a phenol resin, an epoxy resin, a melamine resin, or a polyimide resin is provided as a heat-resistant protective layer on the back surface of the support to improve the heat resistance of the support.
【0018】本発明に使用される熱溶融性インク層に
は、従来から公知の各種材料が使用され、着色材として
は有機および無機の顔料あるいは染料が使用されるが、
好ましくは十分な濃度を持ち耐光性等に優れたものが使
用される。For the hot-melt ink layer used in the present invention, various conventionally known materials are used, and as a coloring material, organic and inorganic pigments or dyes are used.
Preferably, those having a sufficient concentration and excellent in light resistance and the like are used.
【0019】熱溶融性インク層のワックス成分として
は、カルナバワックス、キャンデリラワックス、モンタ
ンワックス、木ロウ、ミツロウ、パラフィンワックス、
マイクロクリスタリンワックス、フィッシャートロプシ
ュワックス、エステルワックス、ポリエチレンワック
ス、ラノリン系ワックス、各種酸化ワックス、ラウリン
酸、ステアリン酸等の高級脂肪酸等が使用される。The wax component of the hot-melt ink layer includes carnauba wax, candelilla wax, montan wax, wood wax, beeswax, paraffin wax,
Microcrystalline wax, Fischer-Tropsch wax, ester wax, polyethylene wax, lanolin-based wax, various oxidized waxes, and higher fatty acids such as lauric acid and stearic acid are used.
【0020】熱溶融性インク層の熱溶融性樹脂成分とし
ては、着色剤およびワックス成分を支持体上に定着しう
る柔軟なエチレン−酢酸ビニル樹脂、エチレン−エチル
アクリレート樹脂等が使用される。As the heat-meltable resin component of the heat-meltable ink layer, a flexible ethylene-vinyl acetate resin, ethylene-ethyl acrylate resin or the like capable of fixing a colorant and a wax component on a support is used.
【0021】[0021]
【実施例】次に実施例により本発明の具体的な説明をす
る。なお、実施例の各成分については重量部または重量
%とする。Next, the present invention will be described in detail with reference to examples. In addition, each component of an Example is set to a weight part or weight%.
【0022】 実施例1 [熱溶融性インク組成] カーボンブラック 15部 分散剤 5部 パラフィンワックス 50部 カルナバワックス 20部 エチレン−酢酸ビニル樹脂 10部 からなる成分を分散処理を行い、熱溶融性インクを得
た。 [塗布液1] スチレン−マレイン酸樹脂 軟化点 135℃ 10部 (10% イソプロピルアルコール溶液) エチルセルロース樹脂 10部 (10% イソプロピルアルコール溶液) シリコン変性樹脂 10部 (10% イソプロピルアルコール溶液) シリコン微粒子 3部 (平均粒子径 2μm 球状) イソプロピルアルコール 50部 を撹拌し塗布液1を得た。次に片面に耐熱処理を施した
厚さ約4.5μmのポリエステルフィルム上に、熱溶融
性インクをホットメルトコーティングにより約6g/平
方メートル塗布し熱溶融性インク層を設け、さらにその
上に塗布液1を乾燥後約0.3g/平方メートルになる
様にコーティングし熱転写記録媒体を得た。Example 1 [Heat-Fusible Ink Composition] Carbon black 15 parts Dispersant 5 parts Paraffin wax 50 parts Carnauba wax 20 parts Ethylene-vinyl acetate resin 10 parts Obtained. [Coating liquid 1] Styrene-maleic acid resin Softening point 135 ° C 10 parts (10% isopropyl alcohol solution) Ethyl cellulose resin 10 parts (10% isopropyl alcohol solution) Silicon modified resin 10 parts (10% isopropyl alcohol solution) Silicon fine particles 3 parts (Average particle diameter: 2 μm, spherical) 50 parts of isopropyl alcohol was stirred to obtain a coating liquid 1. Next, a hot-melt ink is applied by about 6 g / m 2 on a polyester film having a thickness of about 4.5 μm, which is heat-treated on one side, by hot-melt coating to form a hot-melt ink layer. After drying, No. 1 was coated to a thickness of about 0.3 g / m 2 to obtain a thermal transfer recording medium.
【0023】 実施例2および3 実施例1における塗布液1のシリコン微粒子の平均粒子
径を、それぞれ0.5μm、5μmとした以外は同様に
して熱転写記録媒体を得た。Examples 2 and 3 Thermal transfer recording media were obtained in the same manner as in Example 1 except that the average particle diameter of the silicon fine particles of the coating liquid 1 was 0.5 μm and 5 μm, respectively.
【0024】 実施例4および5 実施例1における塗布液1のシリコン微粒子の重量部
を、それぞれ1部、9部とした以外は同様にして熱転写
記録媒体を得た。Examples 4 and 5 A thermal transfer recording medium was obtained in the same manner as in Example 1, except that the parts by weight of the silicon fine particles of the coating liquid 1 were changed to 1 part and 9 parts, respectively.
【0025】 実施例6 実施例1における塗布液1のスチレン−マレイン酸樹脂
を0.031部としエチルセルロース樹脂を除去し、シ
リコン変性樹脂を30部とした以外は同様にして熱転写
記録媒体を得た。Example 6 A thermal transfer recording medium was obtained in the same manner as in Example 1, except that the styrene-maleic acid resin in the coating solution 1 was changed to 0.031 parts, the ethyl cellulose resin was removed, and the silicon-modified resin was changed to 30 parts. .
【0026】 実施例7 実施例1における塗布液1のスチレン−マレイン酸樹脂
を18.5部、シリコン変性樹脂を1.5部とした以外
は同様にして熱転写記録媒体を得た。Example 7 A thermal transfer recording medium was obtained in the same manner as in Example 1 except that the coating liquid 1 was changed to 18.5 parts of styrene-maleic acid resin and 1.5 parts of silicon-modified resin.
【0027】 実施例8 実施例1における塗布液1のシリコン微粒子を、平均粒
子径4μmの不定形二酸化珪素とした以外は同様にして
熱転写記録媒体を得た。Example 8 A thermal transfer recording medium was obtained in the same manner as in Example 1, except that the silicon fine particles of the coating liquid 1 were amorphous silicon dioxide having an average particle diameter of 4 μm.
【0028】 比較例1および2 実施例1における塗布液1のシリコン微粒子の平均粒子
径を、それぞれ0.3μm、6μmとした以外は同様に
して熱転写記録媒体を得た。Comparative Examples 1 and 2 A thermal transfer recording medium was obtained in the same manner as in Example 1, except that the average particle diameter of the silicon fine particles of the coating liquid 1 was 0.3 μm and 6 μm, respectively.
【0029】 比較例3 実施例1における塗布液1のシリコン微粒子を除去した
以外は同様にして熱転写記録媒体を得た。Comparative Example 3 A thermal transfer recording medium was obtained in the same manner as in Example 1, except that the silicon fine particles of the coating liquid 1 were removed.
【0030】 比較例4 実施例1における塗布液1のシリコン微粒子の重量部を
10部とした以外は同様にして熱転写記録媒体を得た。Comparative Example 4 The parts by weight of the silicon fine particles of the coating liquid 1 in Example 1 were
A thermal transfer recording medium was obtained in the same manner except that the amount was 10 parts.
【0031】 比較例5 実施例1における塗布液1のスチレン−マレイン酸樹脂
を20部とし、シリコン樹脂を除去した以外は同様にして
熱転写記録媒体を得た。Comparative Example 5 A thermal transfer recording medium was obtained in the same manner as in Example 1 except that the styrene-maleic acid resin of the coating solution 1 was changed to 20 parts and the silicone resin was removed.
【0032】 比較例6 実施例1における塗布液1のスチレン−マレイン酸樹脂
の軟化点を100℃とした以外は同様にして熱転写記録
媒体を得た。Comparative Example 6 A thermal transfer recording medium was obtained in the same manner as in Example 1 except that the softening point of the styrene-maleic acid resin of the coating solution 1 was changed to 100 ° C.
【0033】 比較例7 実施例1における塗布液1のシリコン微粒子を、熱溶融
性微粒子(ポリエチレンワックス、平均粒子径3μm)
とした以外は同様にして熱転写記録媒体を得た。Comparative Example 7 Silicon fine particles of the coating liquid 1 in Example 1 were used as heat-meltable fine particles (polyethylene wax, average particle diameter 3 μm).
A thermal transfer recording medium was obtained in the same manner except for the above.
【0034】以上15種の熱転写記録媒体を、ラインサ
ーマルプリンターにて以下の条件で、同一箇所を5回印
字した。 [印字条件] サーマルヘッド:ライン薄膜ヘッド(8dot/mm) 印字速度:5インチ/sec 印字エネルギー:18mj/平方ミリメートル 被転写紙:コート紙(べック平滑度300sec)The above 15 kinds of thermal transfer recording media were printed 5 times at the same location by a line thermal printer under the following conditions. [Printing conditions] Thermal head: line thin film head (8 dots / mm) Printing speed: 5 inches / sec Printing energy: 18 mj / square millimeter Transfer receiving paper: coated paper (Beck smoothness 300 sec)
【0035】印字濃度についてはマクベス濃度計TR−
927、印字品質については目視にて評価を行った。結
果は表1のとおりであった。Regarding the print density, a Macbeth densitometer TR-
927, the print quality was visually evaluated. The results were as shown in Table 1.
【0036】[0036]
【表1】 [Table 1]
【0037】[0037]
【発明の効果】以上実施例に記述した様に本発明の熱転
写記録媒体は、印字回数に関係なく高濃度かつ高品質の
印字画像が得られるものである。As described in the above embodiments, the thermal transfer recording medium of the present invention can provide a high-density and high-quality printed image regardless of the number of times of printing.
Claims (4)
らにその上層に転写制御層を設けた多数回熱転写記録媒
体において、転写制御層が非熱軟化性または高軟化点を
有する被膜形成樹脂成分と熱溶融性インクおよび受像紙
に対して離型作用を有する事を目的とした離型性樹脂成
分とからなる転写制御層形成樹脂と、非熱溶融性微粒子
とからなることを特徴とした多数回熱転写記録媒体。1. A multi-time thermal transfer recording medium in which a heat-fusible ink layer is provided on a support, and a transfer control layer is further provided thereon, in which a transfer control layer has a non-softening property or a high softening point. A transfer control layer forming resin comprising a resin component, a heat-meltable ink and a release resin component for the purpose of having a releasing effect on an image receiving paper, and non-heat-meltable fine particles. Many times thermal transfer recording medium.
μm〜5μmの微粉末粒子であり、かつ非熱溶融性微粒
子と前記転写制御層形成樹脂の重量比が25:75〜7
5:25であることを特徴とした請求項1の多数回熱転
写記録媒体。2. The non-heat-fusible fine particles have an average particle diameter of 0.5.
μm to 5 μm, and the weight ratio of the non-heat-meltable fine particles to the resin for forming the transfer control layer is 25:75 to 7
5. The multi-time thermal transfer recording medium according to claim 1, wherein the ratio is 5:25.
℃以上の樹脂で形成し、かつ離型性樹脂成分は、シリコ
ーン樹脂、シリコーン変性樹脂、フッ素系樹脂の1種ま
たは複数を含有し、被膜形成樹脂成分と離型性樹脂成分
の重量比が0.1:99.9〜95:5であることを特
徴とした請求項1の多数回熱転写記録媒体。3. The film-forming resin component has a softening point of 130.
C. or higher, and the release resin component contains one or more of a silicone resin, a silicone-modified resin, and a fluorine-based resin, and the weight ratio of the film-forming resin component to the release resin component is 0. 2. The multi-time thermal transfer recording medium according to claim 1, wherein the ratio is 1: 99.9 to 95: 5.
/平方メートル〜1.0g/平方メートルとすることを
特徴とした請求項1および3の多数回熱転写記録媒体。4. The coating amount of the transfer control layer is 0.05 g.
4. The thermal transfer recording medium according to claim 1, wherein the density of the thermal transfer recording medium is from 1.0 g / m 2 to 1.0 g / m 2.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9291523A JPH11105442A (en) | 1997-10-07 | 1997-10-07 | Many times thermal transfer recording medium to be used |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9291523A JPH11105442A (en) | 1997-10-07 | 1997-10-07 | Many times thermal transfer recording medium to be used |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH11105442A true JPH11105442A (en) | 1999-04-20 |
Family
ID=17770011
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9291523A Pending JPH11105442A (en) | 1997-10-07 | 1997-10-07 | Many times thermal transfer recording medium to be used |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH11105442A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7067457B2 (en) | 2003-09-17 | 2006-06-27 | Eastman Kodak Company | Thermal donor for high-speed printing |
| US7135433B2 (en) | 2003-09-17 | 2006-11-14 | Eastman Kodak Company | Thermal print assembly |
-
1997
- 1997-10-07 JP JP9291523A patent/JPH11105442A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7067457B2 (en) | 2003-09-17 | 2006-06-27 | Eastman Kodak Company | Thermal donor for high-speed printing |
| US7135433B2 (en) | 2003-09-17 | 2006-11-14 | Eastman Kodak Company | Thermal print assembly |
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