JPH02310088A - Wax for thermal transfer recording medium - Google Patents
Wax for thermal transfer recording mediumInfo
- Publication number
- JPH02310088A JPH02310088A JP1132473A JP13247389A JPH02310088A JP H02310088 A JPH02310088 A JP H02310088A JP 1132473 A JP1132473 A JP 1132473A JP 13247389 A JP13247389 A JP 13247389A JP H02310088 A JPH02310088 A JP H02310088A
- Authority
- JP
- Japan
- Prior art keywords
- wax
- heat
- fusion
- eutectic mixture
- fatty acid
- 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 description 32
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 21
- 229930195729 fatty acid Natural products 0.000 claims abstract description 21
- 239000000194 fatty acid Substances 0.000 claims abstract description 21
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 21
- 239000000374 eutectic mixture Substances 0.000 claims abstract description 19
- 230000004927 fusion Effects 0.000 claims abstract description 16
- 239000000126 substance Substances 0.000 claims abstract description 16
- 239000007787 solid Substances 0.000 claims abstract description 12
- 239000004480 active ingredient Substances 0.000 claims description 3
- 239000001993 wax Substances 0.000 abstract description 42
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 abstract description 20
- 239000000203 mixture Substances 0.000 abstract description 15
- 235000021357 Behenic acid Nutrition 0.000 abstract description 10
- 229940116226 behenic acid Drugs 0.000 abstract description 10
- 235000013869 carnauba wax Nutrition 0.000 abstract description 10
- 239000004203 carnauba wax Substances 0.000 abstract description 10
- 239000012170 montan wax Substances 0.000 abstract description 8
- 235000021355 Stearic acid Nutrition 0.000 abstract description 6
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 abstract description 6
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 abstract description 6
- 239000008117 stearic acid Substances 0.000 abstract description 6
- 238000002156 mixing Methods 0.000 abstract description 4
- 230000000694 effects Effects 0.000 abstract description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 3
- 239000000976 ink Substances 0.000 description 15
- 230000008018 melting Effects 0.000 description 14
- 238000002844 melting Methods 0.000 description 14
- -1 polyethylene Polymers 0.000 description 5
- WCOXQTXVACYMLM-UHFFFAOYSA-N 2,3-bis(12-hydroxyoctadecanoyloxy)propyl 12-hydroxyoctadecanoate Chemical compound CCCCCCC(O)CCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCC(O)CCCCCC)COC(=O)CCCCCCCCCCC(O)CCCCCC WCOXQTXVACYMLM-UHFFFAOYSA-N 0.000 description 4
- 238000001938 differential scanning calorimetry curve Methods 0.000 description 4
- 239000000123 paper Substances 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 241000209094 Oryza Species 0.000 description 3
- 235000007164 Oryza sativa Nutrition 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000004359 castor oil Substances 0.000 description 3
- 235000019438 castor oil Nutrition 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 235000009566 rice Nutrition 0.000 description 3
- ULQISTXYYBZJSJ-UHFFFAOYSA-N 12-hydroxyoctadecanoic acid Chemical compound CCCCCCC(O)CCCCCCCCCCC(O)=O ULQISTXYYBZJSJ-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 235000013871 bee wax Nutrition 0.000 description 2
- 239000012166 beeswax Substances 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
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 239000011343 solid material Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- OKMWKBLSFKFYGZ-UHFFFAOYSA-N 1-behenoylglycerol Chemical compound CCCCCCCCCCCCCCCCCCCCCC(=O)OCC(O)CO OKMWKBLSFKFYGZ-UHFFFAOYSA-N 0.000 description 1
- 229940114072 12-hydroxystearic acid Drugs 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 101150026303 HEX1 gene Proteins 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 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
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000013868 candelilla wax Nutrition 0.000 description 1
- 239000004204 candelilla wax Substances 0.000 description 1
- 229940073532 candelilla wax Drugs 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- PZTQVMXMKVTIRC-UHFFFAOYSA-L chembl2028348 Chemical compound [Ca+2].[O-]S(=O)(=O)C1=CC(C)=CC=C1N=NC1=C(O)C(C([O-])=O)=CC2=CC=CC=C12 PZTQVMXMKVTIRC-UHFFFAOYSA-L 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- ZQPPMHVWECSIRJ-MDZDMXLPSA-N elaidic acid Chemical compound CCCCCCCC\C=C\CCCCCCCC(O)=O ZQPPMHVWECSIRJ-MDZDMXLPSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 235000010187 litholrubine BK Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 235000019809 paraffin wax Nutrition 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 230000036314 physical performance Effects 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- 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
本発明は感熱転写記録媒体用ワックス、より詳しくは単
独でもしくは着色剤その他の添加剤を練合せて、耐熱性
基材表面に塗布することによって、熱転写記録媒体の転
写層(インク層)や剥離層等を形成し得る感熱転写記録
媒体用ワックスに関する。DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention provides a wax for heat-sensitive transfer recording media, more specifically, a wax for heat-sensitive transfer recording media, which is applied alone or mixed with colorants and other additives to the surface of a heat-resistant substrate. The present invention relates to a wax for thermal transfer recording media that can form a transfer layer (ink layer), a release layer, etc. of the thermal transfer recording medium.
従来技術とその問題点
近年、ファクシミリ、コンビコ−一ター末端、ワートプ
ロセッザー、画像レコーダー、プリンター等の各種装置
には、ノンインパクトで騒音か少ないこと、装置の機構
が簡単なこと、低コス]へ、高信頼性、小型軽量化、カ
ラー化可能等の面より、熱転写記録媒体、即ち感熱転写
シートが広く利用されている。該感熱転写シートは、一
般にポリエステル等の耐熱性基材表面に、ワックス等の
熱により液状となる常温固体物質(低融点物質)に着色
剤その他の添加剤を練合したインク層を形成させたもの
であり、このインク層に転写紙を合せ、感熱ヘッドで印
字することによって転写紙に所望の画像等を形成できる
ものである。また上記インク層と耐熱性基材との間に形
成されることのある剥離層も同様にワックス等の低融点
物質が使用されている。Conventional technology and its problems In recent years, various devices such as facsimiles, combination printers, word processors, image recorders, printers, etc. have been developed with the aim of being non-impact, making little noise, having simple device mechanisms, and low cost. Thermal transfer recording media, that is, thermal transfer sheets, are widely used because of their high reliability, small size and light weight, and ability to print in color. The heat-sensitive transfer sheet is generally made by forming an ink layer on the surface of a heat-resistant base material such as polyester, which is made by mixing coloring agents and other additives with a room-temperature solid substance (low melting point substance) such as wax that becomes liquid when heated. By aligning a transfer paper with this ink layer and printing with a thermal head, a desired image or the like can be formed on the transfer paper. Similarly, a low melting point substance such as wax is used for the release layer that may be formed between the ink layer and the heat-resistant base material.
しかして、上記低融点物質としては、従来よりパラフィ
ンワックス、カルナバワックス、キャンデリラワックス
、蜜ロウ等の天然ワックスや、ポリエヂレンワックス、
変性モンタンロウ等の合成ワックス類か利用されている
が、之等【J、いり−れも融解性がシャープでなく、サ
ーマルヘッドからの熱に対する応答が遅く、高速印字性
、印字画像の繊細性に劣るという重大な欠点がある。か
かる融解性がシャープでないものは、また凝固性もシV
−プでなく、融解転写されたインクの同化が遅く、高速
印字時に地汚れ等の起こる欠点も認められる。Conventionally, the low melting point substances mentioned above include natural waxes such as paraffin wax, carnauba wax, candelilla wax, and beeswax, polyethylene wax,
Synthetic waxes such as modified montan wax are used; It has a serious disadvantage of being inferior. Those whose meltability is not sharp also have sharp solidification properties.
However, the assimilation of melt-transferred ink is slow, and disadvantages such as background smearing occur during high-speed printing.
問題点を解決するための手段
本発明者らは、上記現状に鑑み、従来のこの種感熱転写
記録媒体、特にその主成分とする低融点物質(ワックス
)に見られる欠点を解潤し、殊に融解性がシャープな感
熱転写記録媒体用ワックスの開発を目的として鋭意研究
を重ねた。Means for Solving the Problems In view of the above-mentioned current situation, the present inventors have solved the drawbacks of conventional heat-sensitive transfer recording media of this type, especially the low melting point substance (wax) that is the main component thereof, and particularly We conducted extensive research with the aim of developing a wax for thermal transfer recording media with sharp melting properties.
その結果、高級脂肪酸と常温固形物質との共融混合物が
上記1」的に合致するワックスとしての性能を具(#I
vることを児出し、ここに本発明を完成するに至った。As a result, a eutectic mixture of a higher fatty acid and a solid substance at room temperature has a performance as a wax that meets the above criteria 1 (#I).
We have devised this idea and have now completed the present invention.
即ち、本発明1ま高級脂肪酸と常温固形物質との共融混
合物を有効成分として含有し、示差走査熱量計により測
定される5℃幅での最大融解熱量が全融解熱量の50%
以上であることを特徴とする感熱転写記録媒体用ワック
スに係わる。That is, the present invention 1 contains a eutectic mixture of a higher fatty acid and a room-temperature solid substance as an active ingredient, and the maximum heat of fusion in a 5°C range measured by a differential scanning calorimeter is 50% of the total heat of fusion.
The present invention relates to a wax for thermal transfer recording media characterized by the above characteristics.
本発明ワックスは、従来のこの種ワックスの欠点をすべ
て解消したものであり、感熱転写記録媒体用ワックスと
して、インク層及び剥離層に利用して非常に優れた特性
を発揮する。The wax of the present invention eliminates all the drawbacks of conventional waxes of this type, and exhibits very excellent properties when used in the ink layer and release layer as a wax for thermal transfer recording media.
以下、本発明ワックスの有効成分とする上記共融混合物
につき詳述する。Hereinafter, the above-mentioned eutectic mixture used as an active ingredient of the wax of the present invention will be explained in detail.
該混合物は、高級脂肪酸と常温固形物質とを所定割合で
混合融解することにより調製される。ここで用いられる
高級脂肪酸としては、通常の各種の直鎖状もしくは分枝
鎖状飽和もしくは不飽和高級脂肪酸を例示でき、その中
でも炭素数が16以上、好ましくは18〜34の直鎖状
飽和脂肪酸は好適である。上記高級脂肪酸の具体例とし
ては、例えばパルミチン酸、ステアリン酸、エライジン
酸、ベヘン酸、12−ヒドロキシステアリン酸、モンタ
ンワックス脂肪酸、ライスワックス脂肪酸、ライスプラ
ンワックス脂肪酸、カルナバワックス脂肪酸、硬化ヒマ
シ油脂肪酸等を例示できる。之等はその1種を単独で用
いてもよくまた2種以上を併用することもできる。之等
の中でも特にステアリン酸、ベヘン酸、モンタンワック
ス脂肪酸等は、融解シャープ性の改善に著しい効果を秦
し得るので好ましい。The mixture is prepared by mixing and melting a higher fatty acid and a room temperature solid substance in a predetermined ratio. Examples of the higher fatty acids used here include various ordinary linear or branched saturated or unsaturated higher fatty acids, among which linear saturated fatty acids having 16 or more carbon atoms, preferably 18 to 34 carbon atoms. is suitable. Specific examples of the higher fatty acids include palmitic acid, stearic acid, elaidic acid, behenic acid, 12-hydroxystearic acid, montan wax fatty acid, rice wax fatty acid, rice plan wax fatty acid, carnauba wax fatty acid, hydrogenated castor oil fatty acid, etc. can be exemplified. One of these may be used alone, or two or more may be used in combination. Among these, stearic acid, behenic acid, montan wax fatty acid and the like are particularly preferred because they can have a remarkable effect on improving melt sharpness.
また常温固形物質としては、通常のワックス類、例えば
カルナバワックス、モンタンワックス、カスターワック
ス、パラフィンワックス、ギャンデリラワックス、ライ
スプランワックス、蜜ロウ等の天然ワックスやポリエチ
レンワックス、変性モンタンワックス、ベヘン酸グリセ
ロール等の合成ワックスを例示できる。Examples of solid substances at room temperature include ordinary waxes, such as natural waxes such as carnauba wax, montan wax, castor wax, paraffin wax, ganderilla wax, rice plan wax, and beeswax, polyethylene wax, modified montan wax, and glycerol behenate. Examples include synthetic waxes such as.
上記高級脂肪酸と常温固形物質との)庁舎割合は、混合
物が共融混合物を形成できることを前提として、両者の
組合せにより適宜決定される。例えばベヘン酸とカルナ
バワックスの場合、ベヘン酸1001部に対してカルナ
バワックス約23重量部及び約120重量部の2点に共
融混合物組成が存在する。本発明ワックスはかかる厳密
な共融混合物組成である必要はなく、この付近の組成で
あればよい。かかる組成及び他の組合せの場合の共融混
合物を形成する組成の近似値は、それぞれ後記する実施
例に示す通りである。本発明者らは上記共融混合物が殊
にシャープな融解性を発揮し、該共融混合物の純度が高
い程、上記融解性がシャープとなることを初めて発見し
、この知見により本発明を完成したのである。しかして
、上記共融混合物の形成は、混合物の融解熱量を示差操
作熱量計により測定した時、各成分単独の融解ピークと
同じ位置にピークが現れるか(単に二成分が混ざり合っ
ているだ(プ)、該ピークが異なる位置に現れるか(共
融混合物を形成している)により判断できる。しかるに
上記二成分か単に混ざり合っているだ()で、之等が共
融混合物を形成しない場合1.t、本発明に特有の融解
性のシャープさは得難くなる。The proportion of the above-mentioned higher fatty acid and room-temperature solid substance is determined as appropriate based on the combination of the two, on the premise that the mixture can form a eutectic mixture. For example, in the case of behenic acid and carnauba wax, eutectic mixture compositions exist at two points: about 23 parts by weight and about 120 parts by weight of carnauba wax based on 1001 parts of behenic acid. The wax of the present invention does not need to have such a strict eutectic mixture composition, but may have a composition around this range. Approximate values of the compositions forming the eutectic mixtures for such compositions and other combinations are as shown in the Examples below. The present inventors discovered for the first time that the above-mentioned eutectic mixture exhibits particularly sharp melting properties, and the higher the purity of the eutectic mixture, the sharper the above-mentioned melting properties become. Based on this knowledge, the present invention was completed. That's what I did. Therefore, when the heat of fusion of the mixture is measured using a differential operation calorimeter, the formation of the above-mentioned eutectic mixture can be explained by whether a peak appears at the same position as the melting peak of each component alone (i.e., the two components are simply mixed together). It can be judged by whether the peaks appear at different positions (forming a eutectic mixture). However, if the two components mentioned above are simply mixed together (), and these do not form a eutectic mixture, 1.t, it becomes difficult to obtain the sharpness of melting property characteristic of the present invention.
本発明の感熱転写記録媒体用ワックス(は、上記高級脂
肪酸と常温固形物質との共融混合物を従来のこの種感熱
転写記録媒体用常温固体物質に代替使用して感熱転写イ
ンクや剥離層等の感熱転写記録媒体に調製できる。2等
感熱転写記録媒体の調製は、本発明ソックスを用いるこ
とを除いて通常の方法に従い実施できる。例えば感熱転
写インクは本発明ソックスをカーボンシラツク、フタロ
シアニングリーン、ブリリアントカーミン6B等の着色
剤、その他の添加剤、例えばエチレン酢酸ビニル系樹脂
、アクリル系樹脂、塩化ビニル−酢酸ビニル共重合体樹
脂等の膜質改質剤、流動パラフィン、DOP、ヒマシ油
等の可塑剤、1ヘルエン、キシレン、酢酸エチル等の溶
剤等とプレミキシング後、ボールミル、ザンドミル、ア
1〜ライター、三本ロール等の分散機を用いて練合分散
させることによって調製できる。The wax for thermal transfer recording media of the present invention (is a eutectic mixture of the above-mentioned higher fatty acids and a solid material at room temperature) which can be used as an alternative to the conventional solid material at room temperature for this kind of thermal transfer recording media to produce thermal transfer inks, release layers, etc. A heat-sensitive transfer recording medium can be prepared. A second-class heat-sensitive transfer recording medium can be prepared according to a conventional method except for using the sock of the present invention. For example, the heat-sensitive transfer ink can be prepared by using the sock of the present invention with carbon silk, phthalocyanine green, carbon silk, phthalocyanine green, Coloring agents such as brilliant carmine 6B, other additives, film quality modifiers such as ethylene vinyl acetate resin, acrylic resin, vinyl chloride-vinyl acetate copolymer resin, plasticizers such as liquid paraffin, DOP, castor oil, etc. It can be prepared by pre-mixing with a solvent such as 1-helene, xylene, ethyl acetate, etc., and then kneading and dispersing using a dispersing machine such as a ball mill, a sand mill, an A1-lighter, or a three-roll mill.
上記感熱転写インクの調製に当って、本発明ワックスl
j1、通常)qられるインク固形分に対して約5〜95
重量%、好ましくは約10〜90重量%の範囲で用いら
れるのが適当て市る。In preparing the above thermal transfer ink, the wax l of the present invention
j1, usually) about 5 to 95 to the solid content of the ink
% by weight, preferably in the range of about 10-90% by weight.
かくして得られるインクは、常法に従いこれを耐熱性基
材、例えばポリエステル、ポリプロピレン、ポリスチレ
ン、ポリカーボネート、ポリイミド、その伯の耐熱性プ
ラスチックフィルム、紙、金属箔等に、塗布してインク
層を形成させて、熱転写記録媒体として実用できる。The ink thus obtained is applied to a heat-resistant substrate such as polyester, polypropylene, polystyrene, polycarbonate, polyimide, heat-resistant plastic film, paper, metal foil, etc. to form an ink layer in accordance with a conventional method. Therefore, it can be put to practical use as a thermal transfer recording medium.
発明の効果
本発明ワックスは、融解性がシャープで市ることをその
最大の特徴としてa3す、その利用によって容易に感熱
転写インク等を調製でき、得られる感熱転写記録媒体は
サーマルヘッドとの熱応答が1ばらしく、高速印字でも
感度の優れた良好な印字を1qることができる。Effects of the Invention The wax of the present invention has a sharp melting property and is commercially available. By using it, thermal transfer inks, etc. can be easily prepared, and the resulting thermal transfer recording medium can be heated easily with the thermal head. The response is excellent, and it is possible to print 1q with excellent sensitivity even at high speed printing.
実 施 例
以下、本発明感熱転写記録媒体用ワックスの製造例を実
施例として挙げ、本発明を更に詳しく説明する。EXAMPLES Hereinafter, the present invention will be explained in more detail by referring to examples of manufacturing the wax for thermal transfer recording media of the present invention.
実施例 1
ステアリン酸(日本油脂社製、ステアリン酸NAΔ−1
80)80gに、ライスプランワックス(野田ワックス
社製)20Ωを加え100℃まで加熱撹拌して、本発明
ワックスを調製した。Example 1 Stearic acid (manufactured by NOF Corporation, stearic acid NAΔ-1
80) 20Ω of Rice Plan wax (manufactured by Noda Wax Co., Ltd.) was added to 80 g, and the mixture was heated and stirred to 100° C. to prepare the wax of the present invention.
実施例 2〜9
実施例1と同様にして、下記各高級脂肪酸と常温固形物
質とを所定割合で用いて、第1表に示す本発明ワックス
を調製した。Examples 2 to 9 In the same manner as in Example 1, the waxes of the present invention shown in Table 1 were prepared using the following higher fatty acids and normal temperature solid substances in predetermined ratios.
ベヘン酸・・・クローダーケミカル製、85/90ベヘ
ニン酸
硬化ヒマシ油脂肪酸・・・伊藤製油社製カルナバワック
ス(1号)・・・山口化成社製モンタンワックス・・・
ヘキス1〜社製「ヘキス1〜ワツクスS」
カスターワックス・・・豊田製油社製
上記各例で得られたワックスにつき、以下の物性及び感
熱転写記録媒体用ワックスとしての性能をそれぞれ測定
、評価した。Behenic acid: manufactured by Crowder Chemical, 85/90 Behenic acid hydrogenated castor oil fatty acid: Carnauba wax (No. 1) manufactured by Ito Oil Co., Ltd.: Montan wax manufactured by Yamaguchi Kasei Co., Ltd.
"Hex 1-Wax S" manufactured by Hex 1~ Co., Ltd. Castor wax: Manufactured by Toyota Oil Co., Ltd. The following physical properties and performance as a wax for thermal transfer recording media were measured and evaluated for the waxes obtained in each of the above examples. .
0融点:JIS K 2235 5・3による。0 melting point: According to JIS K 2235 5.3.
0全融解熱及び5℃幅融解熱量:示
差走査熱量計(マツクザイエンスDS(、−3100)
にて、10℃/分の加熱速度で測定しDSC曲線を作製
する。測定試料は2〜3mgとする。0 Total heat of fusion and 5°C width Heat of fusion: Differential scanning calorimeter (Matsukuxience DS (-3100)
Measurements are made at a heating rate of 10° C./min to create a DSC curve. The sample to be measured is 2 to 3 mg.
全融解熱は上記DSC曲線とそのベースラインで囲まれ
た部分の面積から算出する。The total heat of fusion is calculated from the area of the portion surrounded by the DSC curve and its baseline.
また5℃幅融解熱量は、上記DSC曲線に5℃幅で縦軸
に平行の二本の直線をひき、之等直線と上記DSC曲線
及びベースラインで囲まれた部分の面積としで算出され
る。この5℃幅融解熱量が最大となるものを5℃幅最大
融解熱量とする。The 5°C width heat of fusion is calculated by drawing two straight lines parallel to the vertical axis with a 5°C width on the above DSC curve, and taking the area surrounded by the equal straight lines, the above DSC curve, and the baseline. . The maximum heat of fusion in the 5°C width is defined as the maximum heat of fusion in the 5°C width.
0融解シャープ性:
5℃幅最大融解熱量か全融解熱量の50%以上の・しの
をシA・−プ性良好とづる。0 Melting sharpness: 5° C. maximum heat of fusion or 50% or more of the total heat of fusion is defined as good sharpness.
0印字性:下記方法に従い測定評価する。0 Printability: Measure and evaluate according to the following method.
(1)熱転写記録シートの調製
内容7Qm12のステンレス製円筒カップに上記各実施
例で得られたワックス試料の50及びエチレン酢酸ビニ
ル樹脂(エバフレックス45、三井デュポンボ1ノケミ
カル株式会社製)0.20をとり、トルエン20gを加
えて溶解させ、この中にカーボンブラック(MAioo
、三菱化成社製)1.5C]及び直径1mmのカラスビ
ーズ20Qを入れ、円盤型撹拌機で30分間分散させて
試験インキを作製づる。このインキを厚さ6μmのポリ
エチレンフィルム上にバー]レータ−を用いて10μm
ηの塗膜厚さとなるように塗布し、100′Cで2分間
熱風乾して熱転写記録シーIへを作製する。(1) Preparation details of thermal transfer recording sheet 50% of the wax sample obtained in each of the above examples and 0.20% of ethylene vinyl acetate resin (Evaflex 45, manufactured by Mitsui Dupontbo 1 No Chemical Co., Ltd.) were placed in a 7Qm12 stainless steel cylindrical cup. Add 20g of toluene to dissolve it, and add carbon black (MAiooo) to it.
(manufactured by Mitsubishi Kasei Corporation) 1.5C] and crow beads 20Q with a diameter of 1 mm were added and dispersed for 30 minutes using a disk type stirrer to prepare a test ink. This ink was applied onto a polyethylene film with a thickness of 6 μm using a bar plater to form a 10 μm thick film.
The coating was applied to a coating thickness of η and dried with hot air at 100'C for 2 minutes to prepare a thermal transfer recording sheet I.
(2)印字性の測定・評価
上記(1)で得られた各シー]へを、エプソンワードパ
ンクLX王にて、熱転写用紙(エプソン販売株式会社製
品、#8785)に印字し、白抜け、かすれ、地汚れの
有無を目視判定し、之等のないものを印字性良好とする
。(2) Measurement/Evaluation of Printability Each sheet obtained in (1) above was printed on thermal transfer paper (#8785, manufactured by Epson Sales Co., Ltd.) using an Epson Word Punk LX King. The presence or absence of fading and background smearing is visually determined, and those without such markings are considered to have good printability.
)qられた結果を下記第1表に示ず。) The results obtained are not shown in Table 1 below.
また第1表には、比較のため、ステア1ノン酸とカスタ
ーワックスとの共融混合物を形成しない組成での混合物
並びにカルナバワックス、カスターワックス及びモンタ
ンワックスのそれぞれ単独についての同特性値を併記す
る。For comparison, Table 1 also lists the same characteristic values for a mixture of stearic acid and castor wax in a composition that does not form a eutectic mixture, and for each of carnauba wax, castor wax, and montan wax alone. .
更に上記各供試ワックスのDSCチャートを第1図乃至
第14図に示す。Furthermore, DSC charts of each of the above sample waxes are shown in FIGS. 1 to 14.
以上の結果より、本発明のワックス#J、、感熱転写記
録媒体用ワックスとして、非常に優れたものであること
か判る。From the above results, it can be seen that the wax #J of the present invention is extremely excellent as a wax for thermal transfer recording media.
図面の簡単な説明
第1図へ一第13図4′、A、実施例で調製した本発明
ワックス及び比較ワックスのそれぞれにつき、示差走査
熱量計にて測定した融解性を示すDSCヂャ〜1・であ
る。BRIEF DESCRIPTION OF THE DRAWINGS Figure 1 - Figure 13 4', A DSC diagram showing the melting properties measured by differential scanning calorimeter for each of the inventive waxes prepared in the examples and the comparative waxes. It is.
(以 上) (S/120田) ○S。(that's all) (S/120 field) ○S.
(S/1120田) ○50 (S/120田) ○5O (S/190田) ○S0 (S/190山) ○50 (S/190田) ○5O (S/190LLl) 0S0 (S/1eOLU) ○SO (S/190tJJ) :)SO (s/1eouJ) ○5O (S/190田) ○S0(S/1120 field) ○50 (S/120 field) ○5O (S/190 field) ○S0 (S/190 mountain) ○50 (S/190 field) ○5O (S/190LLl) 0S0 (S/1eOLU) ○SO (S/190tJJ) :) SO (s/1eouJ) ○5O (S/190 field) ○S0
Claims (1)
分として含有し、示差走査熱量計により測定される5℃
幅での最大融解熱量が全融解熱量の50%以上であるこ
とを特徴とする感熱転写記録媒体用ワックス。1 Contains a eutectic mixture of higher fatty acids and room temperature solid substances as an active ingredient, and has a temperature of 5°C as measured by a differential scanning calorimeter.
A wax for thermal transfer recording media, characterized in that the maximum heat of fusion in width is 50% or more of the total heat of fusion.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1132473A JPH02310088A (en) | 1989-05-24 | 1989-05-24 | Wax for thermal transfer recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1132473A JPH02310088A (en) | 1989-05-24 | 1989-05-24 | Wax for thermal transfer recording medium |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH02310088A true JPH02310088A (en) | 1990-12-25 |
Family
ID=15082200
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1132473A Pending JPH02310088A (en) | 1989-05-24 | 1989-05-24 | Wax for thermal transfer recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02310088A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1994004618A1 (en) * | 1992-08-19 | 1994-03-03 | The General Electric Company Plc. | Printing inks and method of ink jet printing |
-
1989
- 1989-05-24 JP JP1132473A patent/JPH02310088A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1994004618A1 (en) * | 1992-08-19 | 1994-03-03 | The General Electric Company Plc. | Printing inks and method of ink jet printing |
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