JPH02106393A - Sublimation type thermal transfer recording image receiver - Google Patents
Sublimation type thermal transfer recording image receiverInfo
- Publication number
- JPH02106393A JPH02106393A JP63259319A JP25931988A JPH02106393A JP H02106393 A JPH02106393 A JP H02106393A JP 63259319 A JP63259319 A JP 63259319A JP 25931988 A JP25931988 A JP 25931988A JP H02106393 A JPH02106393 A JP H02106393A
- Authority
- JP
- Japan
- Prior art keywords
- silane coupling
- resin
- coupling agent
- receiving layer
- dye
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000000859 sublimation Methods 0.000 title claims abstract description 9
- 230000008022 sublimation Effects 0.000 title claims abstract description 9
- 239000006087 Silane Coupling Agent Substances 0.000 claims abstract description 21
- 239000013034 phenoxy resin Substances 0.000 claims abstract description 17
- 229920006287 phenoxy resin Polymers 0.000 claims abstract description 17
- 229920005989 resin Polymers 0.000 claims abstract description 16
- 239000011347 resin Substances 0.000 claims abstract description 16
- 239000000758 substrate Substances 0.000 claims description 5
- 239000011248 coating agent Substances 0.000 abstract description 16
- 238000000576 coating method Methods 0.000 abstract description 16
- 230000007062 hydrolysis Effects 0.000 abstract description 7
- 238000006460 hydrolysis reaction Methods 0.000 abstract description 7
- 230000004927 fusion Effects 0.000 abstract description 3
- 239000003960 organic solvent Substances 0.000 abstract description 3
- 239000007787 solid Substances 0.000 abstract description 2
- 238000004519 manufacturing process Methods 0.000 abstract 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 16
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 8
- 229920001296 polysiloxane Polymers 0.000 description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 229930185605 Bisphenol Natural products 0.000 description 5
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- JJQZDUKDJDQPMQ-UHFFFAOYSA-N dimethoxy(dimethyl)silane Chemical compound CO[Si](C)(C)OC JJQZDUKDJDQPMQ-UHFFFAOYSA-N 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- 229920002545 silicone oil Polymers 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 description 3
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 2
- KUBDPQJOLOUJRM-UHFFFAOYSA-N 2-(chloromethyl)oxirane;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound ClCC1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 KUBDPQJOLOUJRM-UHFFFAOYSA-N 0.000 description 2
- 229920001342 Bakelite® Polymers 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 2
- 239000004637 bakelite Substances 0.000 description 2
- JGFBRKRYDCGYKD-UHFFFAOYSA-N dibutyl(oxo)tin Chemical compound CCCC[Sn](=O)CCCC JGFBRKRYDCGYKD-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- JCVQKRGIASEUKR-UHFFFAOYSA-N triethoxy(phenyl)silane Chemical compound CCO[Si](OCC)(OCC)C1=CC=CC=C1 JCVQKRGIASEUKR-UHFFFAOYSA-N 0.000 description 2
- ZYAASQNKCWTPKI-UHFFFAOYSA-N 3-[dimethoxy(methyl)silyl]propan-1-amine Chemical compound CO[Si](C)(OC)CCCN ZYAASQNKCWTPKI-UHFFFAOYSA-N 0.000 description 1
- OXYZDRAJMHGSMW-UHFFFAOYSA-N 3-chloropropyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)CCCCl OXYZDRAJMHGSMW-UHFFFAOYSA-N 0.000 description 1
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical compound C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- 229920002799 BoPET Polymers 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000012461 cellulose resin Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- KQAHMVLQCSALSX-UHFFFAOYSA-N decyl(trimethoxy)silane Chemical compound CCCCCCCCCC[Si](OC)(OC)OC KQAHMVLQCSALSX-UHFFFAOYSA-N 0.000 description 1
- OSXYHAQZDCICNX-UHFFFAOYSA-N dichloro(diphenyl)silane Chemical compound C=1C=CC=CC=1[Si](Cl)(Cl)C1=CC=CC=C1 OSXYHAQZDCICNX-UHFFFAOYSA-N 0.000 description 1
- AHUXYBVKTIBBJW-UHFFFAOYSA-N dimethoxy(diphenyl)silane Chemical compound C=1C=CC=CC=1[Si](OC)(OC)C1=CC=CC=C1 AHUXYBVKTIBBJW-UHFFFAOYSA-N 0.000 description 1
- LIKFHECYJZWXFJ-UHFFFAOYSA-N dimethyldichlorosilane Chemical compound C[Si](C)(Cl)Cl LIKFHECYJZWXFJ-UHFFFAOYSA-N 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000005055 methyl trichlorosilane Substances 0.000 description 1
- JLUFWMXJHAVVNN-UHFFFAOYSA-N methyltrichlorosilane Chemical compound C[Si](Cl)(Cl)Cl JLUFWMXJHAVVNN-UHFFFAOYSA-N 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 125000000951 phenoxy group Chemical class [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 239000005054 phenyltrichlorosilane Substances 0.000 description 1
- 239000000049 pigment 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
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- ORVMIVQULIKXCP-UHFFFAOYSA-N trichloro(phenyl)silane Chemical compound Cl[Si](Cl)(Cl)C1=CC=CC=C1 ORVMIVQULIKXCP-UHFFFAOYSA-N 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は熱昇華性染料を含有した転写層を有する熱転写
記録媒体と組み合わせて使用される昇華型熱転写用受像
体に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a sublimation type thermal transfer image receptor used in combination with a thermal transfer recording medium having a transfer layer containing a thermal sublimable dye.
[従来の技術]
従来、昇華型熱転写記録方式で熱転写インクシート中の
昇華性染料を加熱転写せしめて画像が記録される受像体
の染料受容層用樹脂としては、ポリエステル樹脂が主に
使用され、この他に塩ビー酢ビ樹脂、ポリスチレン、セ
ルロース樹脂などがたまに特許などでみられる。これら
の樹脂は染料の染告性はよいものの、耐熱性が低いため
、記録時にインクシートと融着してしまうという問題点
があり、これを解決するために通常はこれらの樹脂にシ
リコーンオイル等の離型剤を含有させる必要があり、そ
のために記録後の画像の保存性が低下するという欠点が
あった。[Prior Art] Conventionally, polyester resins have been mainly used as resins for the dye-receiving layer of image receptors on which images are recorded by heat-transferring sublimable dyes in a thermal transfer ink sheet using a sublimation-type thermal transfer recording method. In addition, patents are sometimes found for vinyl chloride, vinyl acetate resin, polystyrene, cellulose resin, etc. Although these resins have good dyeing properties, they have low heat resistance, so they have the problem of fusing with the ink sheet during recording.To solve this problem, these resins are usually coated with silicone oil, etc. It is necessary to contain a mold release agent, which has the disadvantage that the storage stability of images after recording is deteriorated.
[発明が解決しようとする課題]
本発明は、こうした実情に鑑み、インクシートに熱融着
することがなく、かつ、耐光性、保存性にも優れた画像
を形成することができる昇華型熱転写用受像体を提供す
ることを目的とするものである。[Problems to be Solved by the Invention] In view of these circumstances, the present invention provides a sublimation thermal transfer that does not cause thermal adhesion to an ink sheet and can form images with excellent light resistance and storage stability. The object of the present invention is to provide an image receptor for use in the present invention.
[課題を解決するための手段]
本発明者らは、上記課題を解決するため、従来より検討
を重ねてきたが、染料受容層用樹脂としてシランカップ
リング剤の部分加水分解物で変性したフェノキシ樹脂を
選択することが有効であることを見出だし、本発明に至
った。[Means for Solving the Problems] In order to solve the above problems, the present inventors have made repeated studies, and found that phenoxy modified with a partial hydrolyzate of a silane coupling agent was used as a resin for the dye-receiving layer. We have discovered that it is effective to select the resin, and have arrived at the present invention.
すなわち、本発明は、基体上に昇華性染料が染着可能な
染料受容層を有する受像体において、該受容層がフェノ
キシ樹脂をシランカップリング剤の部分加水分解物で変
性した樹脂より主としてなる昇華型熱転写記録用受像体
である。That is, the present invention provides an image receptor having a dye-receiving layer on a substrate to which a sublimable dye can be dyed, in which the receptor layer is made mainly of a resin obtained by modifying a phenoxy resin with a partial hydrolyzate of a silane coupling agent. This is an image receptor for type thermal transfer recording.
本発明における染料受容層は、上記のようにフェノキシ
樹脂とシランカップリング剤の部分加水分解物より主と
してなるが、該部分加水分解物はフェノキシ樹脂に対し
て1.0重量%以上、50重量%未満の範囲で使用され
る。染料受容層は、これらを適当な有機溶媒に溶解ない
し分散させて得た塗工液を基体に塗布して形成すること
ができる。The dye-receiving layer in the present invention is mainly composed of a partial hydrolyzate of a phenoxy resin and a silane coupling agent as described above, and the partial hydrolyzate is 1.0% by weight or more and 50% by weight based on the phenoxy resin. Used within the range below. The dye-receiving layer can be formed by dissolving or dispersing these in an appropriate organic solvent and applying a coating solution to the substrate.
ここで使用されるフェノキシ樹脂は二価のフェノール類
とエピクロルヒドリンより合成される樹脂であり、二価
のフェノール類とはビスフェノールA1ジクロルビスフ
エノールA1ビスフエノールF1ビスフエノールACP
、ビスフェノールL1ビスフェノールv1ビスフェノー
ルSなどである。The phenoxy resin used here is a resin synthesized from divalent phenols and epichlorohydrin, and the divalent phenols are bisphenol A1 dichlorobisphenol A1 bisphenol F1 bisphenol ACP.
, bisphenol L1 bisphenol v1 bisphenol S, and the like.
さらにシランカップリング剤の部分加水分解物は二官能
性シランカップリング剤と三官能性シランカップリング
剤を適宜組み合わせて有機溶剤中で水および酸やアルカ
リ性の触媒を加えて作られる。Further, a partial hydrolyzate of a silane coupling agent is prepared by appropriately combining a difunctional silane coupling agent and a trifunctional silane coupling agent, and adding water and an acid or alkaline catalyst in an organic solvent.
二官能性シランカップリング剤としてはジメチルジクロ
ロシラン、ジフェニルジクロロシラン、ジメチルジメト
キシシラン、ジメチルジェトキシシラン、ジフェニルジ
メトキシシラン、γ−グリシドキシプロピルメチルジェ
トキシシラン、N−β(アミノエチル)γ−アミノプロ
ピルメチルジメトキシシランなどが使用できる。Difunctional silane coupling agents include dimethyldichlorosilane, diphenyldichlorosilane, dimethyldimethoxysilane, dimethyljethoxysilane, diphenyldimethoxysilane, γ-glycidoxypropylmethyljethoxysilane, N-β(aminoethyl)γ- Aminopropylmethyldimethoxysilane and the like can be used.
また三官能性シランカップリング剤としては、メチルト
リクロロシラン、フェニルトリクロルシラン、メチルト
リメトキシシラン、フェニルトリエトキシシラン、デシ
ルトリメトキシシラン、ビニルトリエトキシシラン、γ
−メタクリロキシプロピルトリメトキシシラン、γ−グ
リシドキシプロピルトリメトキシシラン、γ−アミノプ
ロピルトリエトキシシラン、γ−クロロプロピルトリメ
トキシシランなどが使用できる。In addition, trifunctional silane coupling agents include methyltrichlorosilane, phenyltrichlorosilane, methyltrimethoxysilane, phenyltriethoxysilane, decyltrimethoxysilane, vinyltriethoxysilane, γ
-Methacryloxypropyltrimethoxysilane, γ-glycidoxypropyltrimethoxysilane, γ-aminopropyltriethoxysilane, γ-chloropropyltrimethoxysilane, etc. can be used.
また本発明においては、染料受容層中にアミノ変性シリ
コーン、エポキシ変性シリコーン、アルキッド変性シリ
コーン等の離型剤を含有させることができる。これらシ
リコーン類の使用により、転写媒体との熱融着防止効果
が更に向上する。しかし、シリコーン含有量が多くなる
と、前期したように記録後の保存性が低下するので、そ
の含有量は染料受容層の樹脂量に対して、10重量%以
下であることが望ましい。Further, in the present invention, a release agent such as amino-modified silicone, epoxy-modified silicone, alkyd-modified silicone, etc. can be contained in the dye-receiving layer. Use of these silicones further improves the effect of preventing heat fusion with the transfer medium. However, as the silicone content increases, the storage stability after recording deteriorates as described above, so the silicone content is desirably 10% by weight or less based on the amount of resin in the dye-receiving layer.
なお、染料受容層中には、充填剤を含有させることもで
きる。充填剤としては、シリカ、酸化チタン、炭酸カル
シウム等の白色顔料が挙げられ、その添加量は、該受容
層の樹脂量に対して、5〜60重量%が好ま、しい。そ
の他、染料受容層には、界面活性剤、紫外線吸収剤、酸
化防止剤などを適宜含有させてもよい。Incidentally, a filler can also be contained in the dye-receiving layer. Examples of fillers include white pigments such as silica, titanium oxide, and calcium carbonate, and the amount added is preferably 5 to 60% by weight based on the amount of resin in the receiving layer. In addition, the dye-receiving layer may contain a surfactant, an ultraviolet absorber, an antioxidant, etc. as appropriate.
また、本発明の受像媒体における基体としては、合成紙
、アート紙、上質紙、コート紙、セルロース繊維紙、プ
ラスチックフィルム等が単独で又はそれらの積層体で、
好適に使用される。Further, as the substrate in the image receiving medium of the present invention, synthetic paper, art paper, high quality paper, coated paper, cellulose fiber paper, plastic film, etc. may be used alone or in a laminate thereof.
Preferably used.
なお、上記基体上への染料受容層の塗布量は、固形分量
で、01〜20g/nfが好適である。The coating amount of the dye-receiving layer on the substrate is preferably 01 to 20 g/nf in terms of solid content.
[実施例] 次に実施例を挙げて本発明をさらに詳細に説明する。[Example] Next, the present invention will be explained in more detail with reference to Examples.
実施例 1
ジメチルジメトキシシラン2.4g、メチルトリメトキ
シシラン1.4gをテトラヒドロフラン20m1に溶解
し、1%硫酸0.3mlを加えて3時間室温で撹拌して
加水分解を行った。Example 1 2.4 g of dimethyldimethoxysilane and 1.4 g of methyltrimethoxysilane were dissolved in 20 ml of tetrahydrofuran, 0.3 ml of 1% sulfuric acid was added, and the mixture was stirred at room temperature for 3 hours to perform hydrolysis.
フェノキシ樹脂[PKHH,巴工業(株)製]10gを
テトラヒドロフラン80m1に溶解し、これに上記シラ
ンカップリング剤の加水分解物を加え次いで、硬化触媒
としてジブチル錫オキサイド0.1gを加えて、受容層
用塗工液とした。10 g of phenoxy resin [PKHH, manufactured by Tomoe Kogyo Co., Ltd.] was dissolved in 80 ml of tetrahydrofuran, to which was added the hydrolyzate of the above silane coupling agent, and then 0.1 g of dibutyltin oxide was added as a curing catalyst to form a receptor layer. It was used as a coating liquid.
この塗工液を厚さ約150μmの合成紙(商品名ユポF
PG−150、玉子油化合成紙社製)上にワイヤーバー
を用いて塗布し、80℃で1時間乾燥して厚さ約5μm
の染料受容層を形成させて本発明の受像体を作製した。This coating solution is applied to synthetic paper approximately 150 μm thick (product name: YUPO F).
PG-150 (manufactured by Tamago Yuka Synthetic Paper Co., Ltd.) using a wire bar and dried at 80°C for 1 hour to a thickness of approximately 5 μm.
An image receptor of the present invention was prepared by forming a dye-receiving layer.
比較例 1
シランカップリング剤の加水分解物を加えることなしに
フェノキシ樹脂(PKHH)のみで実施例1と同じ方法
で受容層を形成させて受像体を作製した。Comparative Example 1 An image receptor was prepared by forming a receptor layer using only phenoxy resin (PKHH) in the same manner as in Example 1 without adding a hydrolyzate of a silane coupling agent.
実施例 2
γ−グリシドキシプロピルメチルジェトキシシラン2.
5g、ビニルトリエトキシシラン0.8gをテトラヒド
ロフラン20m1に溶解し、1%硫酸Q、3mlを加え
て3時間室温で撹拌して加水分解を行った。Example 2 γ-glycidoxypropylmethyljethoxysilane2.
5 g of vinyltriethoxysilane and 0.8 g of vinyltriethoxysilane were dissolved in 20 ml of tetrahydrofuran, 3 ml of 1% sulfuric acid Q was added, and the mixture was stirred at room temperature for 3 hours to perform hydrolysis.
フェノキシ樹脂[PKHC1巴工業(株)製]10gを
テトラヒドロフラン80m1に溶解し、これに上記シラ
ンカップリング剤の加水分解物を加え、次いで硬化触媒
としてジブチル錫ジアセテート0.1gを加えて、受容
層用塗工液とした。10 g of phenoxy resin [PKHC1 manufactured by Tomoe Kogyo Co., Ltd.] was dissolved in 80 ml of tetrahydrofuran, the hydrolyzate of the above silane coupling agent was added thereto, and then 0.1 g of dibutyltin diacetate was added as a curing catalyst to form a receptor layer. It was used as a coating liquid.
この塗工液で実施例1と同じ方法で受容層を形成させて
受像体を作製した。A receptor layer was formed using this coating liquid in the same manner as in Example 1 to produce an image receptor.
比較例 2
シランカップリング剤の加水分解物を加えることなしに
フェノキシ樹脂(PKHC)にシリコンオイル(KF3
93、信越化学(株)製]0.5gを加えた塗工液で実
施例1と同じ方法で受容層を形成させて受像体を作製し
た。Comparative Example 2 Silicone oil (KF3) was added to phenoxy resin (PKHC) without adding a hydrolyzate of silane coupling agent.
No. 93, manufactured by Shin-Etsu Chemical Co., Ltd.] A receptor layer was formed in the same manner as in Example 1 using a coating solution to which 0.5 g was added to prepare an image receptor.
実施例 3
ジメチルジメトキシシラン1.2g、フェニルトリエト
キシシラン0.6gをテトラヒドロフラン20m1に溶
解し、1%硫酸0.3mlを加えて3時間室温で撹拌し
て加水分解を行った。Example 3 1.2 g of dimethyldimethoxysilane and 0.6 g of phenyltriethoxysilane were dissolved in 20 ml of tetrahydrofuran, 0.3 ml of 1% sulfuric acid was added, and the mixture was stirred at room temperature for 3 hours to perform hydrolysis.
フェノキシ樹脂[フェノアートYP−50、東部化成(
株)製]10gをテトラヒドロフラン80m lに溶解
し、これに上記シランカップリング剤の加水分解物を加
え、次いで硬化触媒としてジブチル錫オキサイド0.1
gを加えて受容層用塗工液とした。この塗工液で実施例
1と同じ方法で受容層を形成させて受像体を作製した。Phenoxy resin [phenoart YP-50, Tobu Kasei (
Co., Ltd.] was dissolved in 80 ml of tetrahydrofuran, the hydrolyzate of the above silane coupling agent was added thereto, and then 0.1 g of dibutyltin oxide was added as a curing catalyst.
g was added to prepare a receptor layer coating solution. A receptor layer was formed using this coating liquid in the same manner as in Example 1 to produce an image receptor.
比較例 3
シランカップリング剤の加水分解物を加えることなしに
フェノキシ樹脂(フェノアートYP−50)にシリコン
オイル(KF393)0゜5gを加えた塗工液で実施例
1と同じ方法で受容層を形成させて受像体を作製した。Comparative Example 3 A receptor layer was prepared in the same manner as in Example 1 using a coating solution prepared by adding 0.5 g of silicone oil (KF393) to phenoxy resin (Phenoate YP-50) without adding a hydrolyzate of a silane coupling agent. An image receptor was prepared by forming the following.
実施例 4
ジメチルジメトキシシラン1.8g、γ−アミノプロピ
ルトリエトキシシラン0.7gをテトラヒドロフラン2
0m1に溶解し、1%苛性ソーダ水溶液9.5mlを加
えて3時間室温で撹拌して加水分解を行った。Example 4 1.8 g of dimethyldimethoxysilane and 0.7 g of γ-aminopropyltriethoxysilane were added to 2 g of tetrahydrofuran.
0 ml of the solution, 9.5 ml of 1% aqueous sodium hydroxide solution was added thereto, and the mixture was stirred at room temperature for 3 hours to perform hydrolysis.
フェノキシ樹脂(BAKEL ITE、ユニオンカーバ
イト社製)10gをテトラヒドロフラン80m1に溶解
し、これに上記シランカップリング剤の加水分解物を加
え、次いで硬化触媒としてジブチル錫ジアセテート0.
1gを加えて受容層用塗工液とした。この塗工液で実施
例1と同じ方法で受容層を形成させて受像体を作製した
。10 g of phenoxy resin (BAKEL ITE, manufactured by Union Carbide) was dissolved in 80 ml of tetrahydrofuran, the hydrolyzate of the silane coupling agent was added thereto, and then 0.0 g of dibutyltin diacetate was added as a curing catalyst.
1 g was added to prepare a receptor layer coating solution. A receptor layer was formed using this coating liquid in the same manner as in Example 1 to produce an image receptor.
比較例 4
シランカップリング剤の加水分解物を加えることなしに
、フェノキシ樹脂(BAKELITE)にシリコンオイ
ル(KF393)1.0gを加えた塗工液で実施例1と
同じ方法で受容層を形成させて受像体を作製した。Comparative Example 4 A receptor layer was formed in the same manner as in Example 1 using a coating solution prepared by adding 1.0 g of silicone oil (KF393) to phenoxy resin (BAKELITE) without adding a hydrolyzate of a silane coupling agent. An image receptor was prepared.
[受像体の評価]
昇華転写媒体としてバック層にシリコン硬化樹脂膜(厚
さ約1μm)を設けた厚さ6μmのPETフィルム上に
下記処方のインク層用塗液を約1μmの厚さに塗布して
転写媒体を得た。[Evaluation of image receptor] An ink layer coating liquid with the following formulation was applied to a thickness of approximately 1 μm on a 6 μm thick PET film with a silicone cured resin film (approximately 1 μm thick) as a back layer as a sublimation transfer medium. A transfer medium was obtained.
(玉量部)
ポリビニルブチラール樹脂、 10BX−1(漬水
化学社製)
シアン用昇華染料、カヤセット 8
ブルーフ14(日本化薬社製)
トルエン 45
メチルエチルケトン 45
得られた転写媒体と受像体とを、転写媒体のインク層と
受像体の染料受容層とが対面するように重ね合わせ転写
媒体の裏面からサーマルヘッドで加熱エネルギーを変え
て画像記録を行った。なおサーマルヘッドの記録密度は
6ドツト/ m mであり、記録出力は0.42W/ド
ツトであった。(Ball weight part) Polyvinyl butyral resin, 10BX-1 (manufactured by Tsukisui Kagaku Co., Ltd.) Sublimation dye for cyan, Kayaset 8 Bluef 14 (manufactured by Nippon Kayaku Co., Ltd.) Toluene 45 Methyl ethyl ketone 45 The obtained transfer medium and image receptor were The ink layer of the transfer medium and the dye-receiving layer of the image receptor were overlapped so that they faced each other, and images were recorded from the back side of the transfer medium using a thermal head by varying heating energy. The recording density of the thermal head was 6 dots/mm, and the recording output was 0.42 W/dot.
この記録後の画像サンプルについて耐光性等の試験を行
った。それらの結果を第1表に示す。The image samples after recording were tested for light resistance and the like. The results are shown in Table 1.
第1表
注)■画像濃度・・・マクベス濃度計RD−514によ
る■耐光性 ・・キセノンフェードメーで24時間露光
した後、画像の変化を目視で判
定した。○・・・良好、×・・・不良
■保存性 ・・・60℃で暗所に100時間保存した後
、画像の変化を目視で判定した。Table 1 Note) ■Image density: Macbeth densitometer RD-514 ■Lightfastness: After exposure for 24 hours using a xenon fader, changes in the image were visually determined. ○: Good, ×: Poor ■Storability: After being stored in a dark place at 60° C. for 100 hours, changes in the image were visually judged.
○・・良好、×・・不良
■比較例1のサンプルは熱融着のため試験不能であった
。○...Good, ×...Poor ■The sample of Comparative Example 1 could not be tested due to heat fusion.
[発明の効果]
以上説明したように、本発明の構成による受像体は、イ
ンクシートに熱融着せず、しかも耐光性、保存性にすぐ
れた画像を得ることができる。[Effects of the Invention] As described above, the image receptor configured according to the present invention is not thermally fused to an ink sheet and can provide images with excellent light resistance and storage stability.
Claims (2)
する受像体において、該受容層がフェノキシ樹脂をシラ
ンカップリング剤の部分加水分解物で変性した樹脂より
主としてなることを特徴とする昇華型熱転写記録用受像
体(1) An image receptor having a dye-receiving layer on a substrate in which a sublimable dye can be first deposited, characterized in that the receptor layer is mainly made of a resin obtained by modifying a phenoxy resin with a partial hydrolyzate of a silane coupling agent. Image receptor for sublimation thermal transfer recording
部分加水分解物の含有量が1.0重量%以上50重量%
未満である請求項(1)記載の昇華型熱転写記録用受像
体(2) The content of the partial hydrolyzate of the silane coupling agent is 1.0% by weight or more and 50% by weight based on the phenoxy resin.
The image receptor for sublimation type thermal transfer recording according to claim (1), which is less than
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63259319A JP2688504B2 (en) | 1988-10-17 | 1988-10-17 | Sublimation type thermal transfer recording receiver |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63259319A JP2688504B2 (en) | 1988-10-17 | 1988-10-17 | Sublimation type thermal transfer recording receiver |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02106393A true JPH02106393A (en) | 1990-04-18 |
JP2688504B2 JP2688504B2 (en) | 1997-12-10 |
Family
ID=17332429
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63259319A Expired - Fee Related JP2688504B2 (en) | 1988-10-17 | 1988-10-17 | Sublimation type thermal transfer recording receiver |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2688504B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5244862A (en) * | 1992-07-31 | 1993-09-14 | Bailey David B | Thermal dye transfer receiving element with modified bisphenol-A epichlorohydrin polymer dye-image receiving layer |
US5369079A (en) * | 1989-10-04 | 1994-11-29 | Dai Nippon Insatsu Kabushiki Kaisha | Process for making a heat-transferred imaged article |
-
1988
- 1988-10-17 JP JP63259319A patent/JP2688504B2/en not_active Expired - Fee Related
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5369079A (en) * | 1989-10-04 | 1994-11-29 | Dai Nippon Insatsu Kabushiki Kaisha | Process for making a heat-transferred imaged article |
US5244862A (en) * | 1992-07-31 | 1993-09-14 | Bailey David B | Thermal dye transfer receiving element with modified bisphenol-A epichlorohydrin polymer dye-image receiving layer |
EP0581263A2 (en) * | 1992-07-31 | 1994-02-02 | Eastman Kodak Company | Thermal dye transfer receiving element with modified bisphenol-A epichlorohydrin polymer dye-image receiving layer |
Also Published As
Publication number | Publication date |
---|---|
JP2688504B2 (en) | 1997-12-10 |
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