JPS62259848A - Synthetic paper having double layer structure - Google Patents
Synthetic paper having double layer structureInfo
- Publication number
- JPS62259848A JPS62259848A JP61079442A JP7944286A JPS62259848A JP S62259848 A JPS62259848 A JP S62259848A JP 61079442 A JP61079442 A JP 61079442A JP 7944286 A JP7944286 A JP 7944286A JP S62259848 A JPS62259848 A JP S62259848A
- Authority
- JP
- Japan
- Prior art keywords
- synthetic paper
- layer
- weight
- fine powder
- surface layer
- 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
- 239000010410 layer Substances 0.000 claims description 57
- 239000002344 surface layer Substances 0.000 claims description 55
- 239000000843 powder Substances 0.000 claims description 41
- 239000012792 core layer Substances 0.000 claims description 28
- 229920005989 resin Polymers 0.000 claims description 26
- 239000011347 resin Substances 0.000 claims description 26
- 230000006835 compression Effects 0.000 claims description 16
- 238000007906 compression Methods 0.000 claims description 16
- 229920005992 thermoplastic resin Polymers 0.000 claims description 7
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 32
- -1 polyethylene terephthalate Polymers 0.000 description 31
- 238000012546 transfer Methods 0.000 description 31
- 239000000203 mixture Substances 0.000 description 27
- 239000004743 Polypropylene Substances 0.000 description 23
- 229920001155 polypropylene Polymers 0.000 description 23
- 229910000019 calcium carbonate Inorganic materials 0.000 description 16
- 239000000463 material Substances 0.000 description 15
- 239000002245 particle Substances 0.000 description 11
- 229920001577 copolymer Polymers 0.000 description 10
- 239000011342 resin composition Substances 0.000 description 10
- 239000001993 wax Substances 0.000 description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- 238000004040 coloring Methods 0.000 description 9
- 229920001903 high density polyethylene Polymers 0.000 description 9
- 239000004700 high-density polyethylene Substances 0.000 description 9
- 238000001816 cooling Methods 0.000 description 8
- 239000000975 dye Substances 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 6
- 239000004793 Polystyrene Substances 0.000 description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 239000000155 melt Substances 0.000 description 5
- 229920002223 polystyrene Polymers 0.000 description 5
- 239000005977 Ethylene Substances 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 4
- 241000519995 Stachys sylvatica Species 0.000 description 4
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 4
- 239000004927 clay Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 229920001971 elastomer Polymers 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 229920001684 low density polyethylene Polymers 0.000 description 4
- 239000004702 low-density polyethylene Substances 0.000 description 4
- 229920001179 medium density polyethylene Polymers 0.000 description 4
- 239000004701 medium-density polyethylene Substances 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 239000005060 rubber Substances 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 239000011256 inorganic filler Substances 0.000 description 3
- 229910003475 inorganic filler Inorganic materials 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000010023 transfer printing Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- DHKHKXVYLBGOIT-UHFFFAOYSA-N 1,1-Diethoxyethane Chemical compound CCOC(C)OCC DHKHKXVYLBGOIT-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
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- 229920000459 Nitrile rubber Polymers 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000000903 blocking effect Effects 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 210000005069 ears Anatomy 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
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000009499 grossing Methods 0.000 description 2
- 239000001023 inorganic pigment Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000012766 organic filler Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 239000002985 plastic film Substances 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 229920005672 polyolefin resin Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 241000272525 Anas platyrhynchos Species 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000011354 acetal resin Substances 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 229920006243 acrylic copolymer Polymers 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000012164 animal wax Substances 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 239000000981 basic dye Substances 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011362 coarse particle Substances 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 229920006242 ethylene acrylic acid copolymer Polymers 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000012169 petroleum derived wax Substances 0.000 description 1
- 235000019381 petroleum wax Nutrition 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 229920003176 water-insoluble polymer Polymers 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Thermal Transfer Or Thermal Recording In General (AREA)
- Duplication Or Marking (AREA)
- Laminated Bodies (AREA)
- Paper (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明の合成紙は、ポスター用紙、熱転写記録用画像受
容シートの支持体、袋形成用紙材、筆記用紙、コンピュ
ーターホーム用紙等として用いられる。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The synthetic paper of the present invention is used as poster paper, support for image-receiving sheets for thermal transfer recording, bag-forming paper material, writing paper, computer home paper, and the like.
本発明の合成紙は、とりわけ熱転写記録用画像受容シー
トの支持体、とくにサーマルヘッド等のT[気信号によ
り文字や画像を受容体上に形成するビデオプリンター等
に用いるカラーコピー用の支持体として有用である。The synthetic paper of the present invention can be used particularly as a support for image-receiving sheets for thermal transfer recording, and especially as a support for color copying used in video printers and the like that form characters and images on a receptor using a T signal such as a thermal head. Useful.
従来、昇華性又は気化性染料を含有する転写層を有する
転写シートと、受容シートとを重ね合せ、転写シートを
加熱して、転写層に含まれる染料を昇華又は気化させて
受容シートに染着させ、受容シート上に染料画像を形成
させる熱転写は知られている。Conventionally, a transfer sheet having a transfer layer containing a sublimable or vaporizable dye is placed on top of a receiving sheet, and the transfer sheet is heated to sublimate or vaporize the dye contained in the transfer layer and dye the receiving sheet. Thermal transfer is known to produce a dye image on a receiving sheet.
具体的には、サーマルヘッド等の心気信号により制御さ
れる熱源を用いた転写型感熱記録方式では、第1図のよ
うに色材層22と基体21を有する転写体2と、画像受
容層11と支持体12を有する受容シート1をドラム3
と熱源4の間に挟着させて、1気信号に応じて層22の
色材を+i像受容唱11上に転写することによりカラー
コピーを得ている。Specifically, in a transfer type thermal recording method using a heat source controlled by a hypochondrium signal such as a thermal head, as shown in FIG. 11 and a support 12 are placed on a drum 3.
and a heat source 4, and a color copy is obtained by transferring the coloring material of the layer 22 onto the +i image receiving layer 11 in response to a signal.
画像受容層11け、用いる色材の内容により異ゆ、顔料
を含む熱溶融型色材の場合には、支持体12そのものを
用いてよく、昇華性塩基性染料型色材の場合に(d活性
白土(活性クレー)、1を、昇華性分散染料型色材の場
合にはポリエステル等の高分子材料・崎等からなってい
る。従来の受容体では支持体の厚みむら、又は表面凹凸
のため画像受容層11の表面は、5〜15μmの凹凸が
あり、又、1鵡当り10〜20μmのうねりがあった。The content of the image-receiving layer 11 varies depending on the content of the coloring material used; in the case of a heat-melting type coloring material containing a pigment, the support 12 itself may be used, and in the case of a sublimable basic dye type coloring material, (d Activated clay (activated clay) 1 is made of a polymeric material such as polyester in the case of a sublimable disperse dye type coloring material.In the case of a conventional receptor, it is made of a polymeric material such as polyester. Therefore, the surface of the image-receiving layer 11 had irregularities of 5 to 15 μm, and undulations of 10 to 20 μm per duck.
この凹凸又はうねしは、スーパーカレンダーによる表面
処理においても多少の改善がなされるだけで限界があっ
た。このため、色材層22から転写される色材ば、画像
受容層11の表面凹凸が3〜5μm以上又はうねりが1
■当910μm以上では熱溶融色材は勿論、昇華性色材
でも画信号に応じて正確に転写されず、画1象のドツト
ぬけ、ドツト欠は等の画1m2j!品質の乱れを生じ、
中間調にザラツキ基を与えていた(−!?開昭59−2
14696号)。Even surface treatment using a supercalender can only improve the unevenness or undulations to a certain extent. For this reason, when the coloring material is transferred from the coloring material layer 22, the surface unevenness of the image receiving layer 11 is 3 to 5 μm or more, or the waviness is 1 μm or more.
■At 910 μm or more, not only heat-melting coloring materials but also sublimation coloring materials cannot be accurately transferred according to the image signal, resulting in missing dots and missing dots in 1 m2 of images! causing quality disturbances,
It gave a rough texture to the midtones (-!? 1986-2
No. 14696).
また、支持体12としては、紙や無機微細粉末を40〜
50重量%含有する熱可塑性樹脂の延伸フィルムよりな
る合成紙(#f公昭46−40794号)、透明なポリ
エチレンテレフタレートフィルムまたは透明フィルムの
表面に、白色度及び染着性を高めるため、シリカや炭酸
カルシウム等の無機化合物をバインダーと共に表面に塗
正したVn工合成紙等が用いられる。In addition, as the support 12, paper or inorganic fine powder can be used for
Synthetic paper made of stretched film of thermoplastic resin containing 50% by weight (#f Publication No. 46-40794), transparent polyethylene terephthalate film, or transparent film with silica or carbonate on the surface to increase whiteness and dyeability. Vn synthetic paper or the like whose surface is coated with an inorganic compound such as calcium and a binder is used.
熱転写された受容シートのアフターユース(複写、鉛筆
筆記性、保存性等)を考、2ました場合、熱転写記録用
画像受容シートとしては、強度、寸法安定性、無塵性の
面で合成紙やプラスチックフィルムが好ましい。Considering the after-use of the heat-transferred receptor sheet (copying, pencil writing, storage stability, etc.), synthetic paper is recommended as the image-receiving sheet for thermal transfer recording in terms of strength, dimensional stability, and dust-free property. or plastic film is preferred.
しかし、透明なプラスチックフィルムは、複写性に浸れ
るが不透明度が低し、隠蔽性に欠け、画像のコントラス
トが弱いため4’4読しにくい欠点がある。However, although transparent plastic films have good copyability, they have low opacity, lack hiding properties, and have poor image contrast, making them difficult to read.
従って、不透明度が80%以上と高い合成、祇もしくは
透明フィルムの表面に画像受容層を設けた塗工合成紙が
好ましい。Therefore, synthetic paper with a high opacity of 80% or more, or coated synthetic paper with an image-receiving layer provided on the surface of a transparent film is preferred.
しかし、後者の透明フィルムの表面に画像受容層を設け
た塗工合成紙の場合、塗工紙表面に存在する凹凸、ヘッ
ドと受容シートの密着性の不安定さのため鮮明な画像が
得られない。又、裏面の透明フィルムに画像の内容等を
鉛筆等で筆記しようとしても出来ないという欠点を有す
る。However, in the case of coated synthetic paper with an image-receiving layer provided on the surface of a transparent film, clear images cannot be obtained due to the unevenness of the surface of the coated paper and the instability of the adhesion between the head and the receptor sheet. do not have. Another drawback is that even if you try to write the contents of the image on the transparent film on the back side with a pencil or the like, you cannot do so.
一方無機微細粉末を含有する熱可塑性樹脂フィルムの延
呻物よりなる合成紙は熱転写記録用#i像受容シートの
支持体として用いられたときその裏面は鉛筆i配性、耐
水性、無塵性、画像の解読性の面で憂れているが、ヘッ
ドと受gシートとの密着性の不安定さは残っている。即
ち、この延伸フィルムよりなる合成紙は、無機微細粉末
を核とし、延伸により該粉末の周囲に微細な空隙を有し
、表面より該粉末が突出した構造を有する。On the other hand, when synthetic paper made of a rolled thermoplastic resin film containing fine inorganic powder is used as a support for a #i image-receiving sheet for thermal transfer recording, its back surface exhibits pencil-like properties, water resistance, and dust-free properties. Although there are concerns about image decipherability, the adhesion between the head and the gage receiving sheet remains unstable. That is, the synthetic paper made of this stretched film has a structure in which the core is inorganic fine powder, fine voids are formed around the powder by stretching, and the powder protrudes from the surface.
この合成紙において、無機微細粉末として比表面積が1
o、o o oaA/を以上のものを用いても、含有し
ている無機微細粉末の粗大粒子や凝集物が表面より突出
することが有り、この場合、その部分に熱転写された画
像の欠け(白抜け)が生じた獣装置斤を汚染したりする
l17j題がある。In this synthetic paper, the specific surface area is 1 as an inorganic fine powder.
o, o o Even if oaA/ or more is used, coarse particles or aggregates of the contained inorganic fine powder may protrude from the surface, and in this case, the thermally transferred image may be chipped ( There is a problem of contaminating the animal equipment where white spots) occur.
前述の特開昭59−85972号公報は、ドツトの再現
性をよくするため支持体である祇、合成紙の表面に、ペ
ック指数が100〜3000秒の平滑化処理コート層を
設け、この平滑化処理コート層の表面に画像受容層を設
け、画像受g 13の凹凸の突出高さが3ミクロン以下
で、1■当り10ミクロン以内のうねりである熱転写記
録用画鐵受容シートを提案する。The above-mentioned Japanese Patent Application Laid-Open No. 59-85972 discloses that in order to improve the reproducibility of dots, a smoothing coat layer with a Peck index of 100 to 3000 seconds is provided on the surface of synthetic paper as a support. An image receiving sheet for thermal transfer recording is proposed in which an image receiving layer is provided on the surface of a chemically treated coating layer, and the projection height of the image receiving g 13 is 3 microns or less, and the waviness is within 10 microns per inch.
画像の欠けや抜けの問題を解決するためにこのように画
像受容シートの平滑性を増せばよいことは知られている
。しかし、高い平滑を有する画像受容シートでは逆にイ
ンキの画r象受容シートへの転写が不確実となり画像が
不鮮明となるので、適度な平滑性(ペック指数300〜
2500秒)と表面粗さくプリントサーフラフネスが0
.6〜5ミクロン)である熱転写記録用画像受容シート
を用いるのが好ましいことが指摘されている(特開昭6
0−110488号)。It is known that the smoothness of the image-receiving sheet can be increased in this way in order to solve the problem of image chipping and omission. However, with a highly smooth image-receiving sheet, the transfer of ink to the image-receiving sheet becomes uncertain and the image becomes unclear.
2500 seconds) and the surface is rough and the print surf roughness is 0.
.. It has been pointed out that it is preferable to use an image-receiving sheet for thermal transfer recording with a thickness of 6 to 5 microns (Japanese Patent Laid-Open No.
No. 0-110488).
しかし、我々が検討したところによると、支持体にとっ
ては、マクロに見た場合あるf4の粗面、平滑性も必要
であるが、むしろ、支持体の表面より孤立して突出して
いる凸部(突出物)の幅、高さ、ITIA数及び支持体
の合成紙の圧縮性が熱転写印刷時の色抜は防止及び転写
印刷の鮮明性に大きな影響を及ぼす。However, according to our study, although the support requires f4 roughness and smoothness from a macroscopic perspective, it is rather necessary to have a protrusion that is isolated and protrudes from the surface of the support ( The width and height of the protrusions), the ITIA number, and the compressibility of the synthetic paper used as the support have a great effect on preventing color loss during thermal transfer printing and on the clarity of transfer printing.
〔間4点を解決する具体的手段〕
本発明においては、表面層の突出物の幅、高さ、1固数
を、無機微細粉末の含量と表面層の肉厚等の調整により
小さく、低く、少なくして合成紙の表面に平滑性を寸与
し、かつ、既出願の合成紙(′!4開昭60−7995
1号、特開昭61m23748号公報、特頭昭60−2
29353号、同60−290180号明細書)の圧縮
1本8〜18%よりも圧縮率を20〜40%と高くシ、
合成紙にソフト感を与えてヘッドと画1よ受容シートと
のjIj着性を良好にし、転写された印刷がより鮮明と
なるようにした。[Specific means for solving the four points in between] In the present invention, the width, height, and solid number of the protrusions on the surface layer are made smaller and lower by adjusting the content of the inorganic fine powder and the thickness of the surface layer. , to impart smoothness to the surface of the synthetic paper, and to improve the surface smoothness of the synthetic paper ('!4 1986-7995).
No. 1, JP-A-61-23748, Tokuto-Sho 60-2
29353, specification of 60-290180), the compression ratio is 20 to 40%, which is higher than the 8 to 18% compression rate per cylinder.
The synthetic paper was given a soft feel to improve the adhesion between the head and the image receiving sheet, so that the transferred print would be clearer.
即ち、本発明の第1は、(A)無機微細粉末を0〜25
11%含有する熱可塑性樹脂フィルムの表面層と、G)
比表面積が10,000ctd/f以上の無機微細粉末
を表面層の無機Ia@粉末の含有量よや多く含むミクロ
ボイドを多数含有する延伸樹脂フィルム芯層を少なくと
も含有する2層以上の合成紙であって、該合成紙は、
(イ)、圧縮率が20〜40%であって、かつ、(A)
、前記表面層は、その平担面より突出した突出物の最長
長さが50ミクロン以上のものが0.1m’当り10個
以下である
ことを特徴とする複層構造の合成紙を提供するものであ
る。That is, the first aspect of the present invention is that (A) the inorganic fine powder is
a surface layer of a thermoplastic resin film containing 11%; and G)
A synthetic paper with two or more layers containing at least a stretched resin film core layer containing many microvoids containing inorganic fine powder with a specific surface area of 10,000 ctd/f or more than the content of inorganic Ia@ powder in the surface layer. The synthetic paper has (a) a compression ratio of 20 to 40%, and (a)
, to provide a synthetic paper with a multilayer structure, wherein the surface layer has a maximum length of 50 microns or more of protrusions protruding from its flat surface at a rate of 10 or less per 0.1 m'. It is something.
本発明の第2は、第1の合成紙よりもより珀追追記、油
性インクベン膚記の浸れた裏面層を有する合成紙、すな
わち、(AJ無機9細粉末をO〜25重陵%含有する熱
可塑性−!!!4指フィルムの表面層と、(B)比茂面
噴が10,000漏/2以上の無機微細粉末を表面層の
無機微細粉末の含有11より多く含むミクロボイドを多
数含有する・店伸樹脂フィルム中芯層と、0無機微細粉
末を25〜65重欧%含有する延伸樹脂フィルムよりな
る裏面層を少なくとも含有する3層以上の合成紙であっ
て、該合成紙は、
(イ)、圧縮率が20〜40%であって、かつ、←)、
前記表面層(A)は、その平担面より突出した突出物の
最長長さが50ミクロン以上のものが0.1m2当り1
0個以下である
ことを特徴とする復唱構造の合成紙を提供するものであ
る。The second aspect of the present invention is a synthetic paper having a back layer soaked with more oil-based ink than the first synthetic paper. Thermoplastic -!!!The surface layer of the 4-fingered film and (B) Himo surface contain a large number of microvoids containing inorganic fine powder of 10,000 filtration/2 or more, which is more than the content of the inorganic fine powder in the surface layer. - A synthetic paper with three or more layers comprising at least a core layer of a stretched resin film and a back layer made of a stretched resin film containing 25 to 65% by weight of inorganic fine powder, the synthetic paper comprising: (b), the compression ratio is 20 to 40%, and ←),
The surface layer (A) has protrusions that protrude from the flat surface with a maximum length of 50 microns or more at a rate of 1 per 0.1 m2.
To provide a synthetic paper having a repeating structure characterized in that the number of repeating structures is 0 or less.
(樹脂素材)
合成紙の各層を構成する熱可塑性樹脂としては、ポリオ
レフィン樹脂たとえばポリエチレン、ポリプロピレン、
エチレン−プロピレン共重合体、エチレン−酢酸ビニル
共重合体、ポリ(A−メチルペンテン−1)、ポリスチ
レン、ポリアミド、ポリエチレンテレフタレート、エチ
レン−酢酸ビニル共重合体の部分加水分解物、エチレン
−アクリル酸共重合体およびその塩、塩化ビニリデン共
重合体たとえば塩化ビニル−塩化ビニリデン共重合体、
その他、およびこれらの混合物を例示することができる
。これらの中では1酎溶剤性の面ではポリエチレン、ポ
リプロピレン等のポリオレフィン樹脂が好ましい。(Resin material) Thermoplastic resins constituting each layer of synthetic paper include polyolefin resins such as polyethylene, polypropylene,
Ethylene-propylene copolymer, ethylene-vinyl acetate copolymer, poly(A-methylpentene-1), polystyrene, polyamide, polyethylene terephthalate, partial hydrolyzate of ethylene-vinyl acetate copolymer, ethylene-acrylic acid copolymer Polymers and their salts, vinylidene chloride copolymers such as vinyl chloride-vinylidene chloride copolymers,
Others, and mixtures thereof can be exemplified. Among these, polyolefin resins such as polyethylene and polypropylene are preferred in terms of solvent resistance.
(無機微細粉末)
比表面積が10,000 cA/ 9以上の無機質微細
粉末としては炭酸カルシウム、焼成りレイ、ケイ藻土、
タルク、酸化チタン、硫酸バリウム、硫酸アルミニウム
、シリカ等が例示てれる。特に、表面層に配合される無
機微細粉末は表面に大きな突起物を形成しないように3
25メツシユ残が10ppm以下のものが好ましい。(Inorganic fine powder) Examples of the inorganic fine powder with a specific surface area of 10,000 cA/9 or more include calcium carbonate, calcined clay, diatomaceous earth,
Examples include talc, titanium oxide, barium sulfate, aluminum sulfate, and silica. In particular, the inorganic fine powder blended into the surface layer should be carefully
It is preferable that the residual amount of 25 mesh is 10 ppm or less.
(表面層)
表面層(A)は、無機微細粉末を0〜25重1%、好ま
しくは3〜8重a%含有する熱可塑性樹脂フィルムであ
り、このものは配向していても、配向していなくてもよ
い。(Surface layer) The surface layer (A) is a thermoplastic resin film containing 0 to 25% by weight, preferably 3 to 8% by weight, of inorganic fine powder, and this film may be oriented or not. It doesn't have to be.
この表面順回は、色抜防止のため、この表面層の平担面
より突出した突出物の最長長さが50ミクロン以上のも
のが0.1m’当り10個以下好ました表面平滑度(ベ
ック指数)が2,500〜15,000秒と平滑度が高
いものとなるよう無機微細粉末の配合量、種類を選択す
る。In this surface smoothness, in order to prevent discoloration, the maximum length of protrusions protruding from the flat surface of this surface layer is preferably 50 microns or more per 0.1 m' or less.Surface smoothness ( The blending amount and type of the inorganic fine powder are selected so that the smoothness is high and the Beck index is 2,500 to 15,000 seconds.
(中芯層)
中芯層は、合成紙にソフト感を与えるもので、比表面積
が10,000ad/f以上、好ましくは15.000
〜500,000cd/fの無機微細粉末を表面層の無
機微細粉末含有量よりも多く含む(8〜55重量%、好
ましくは10〜25重量%)樹脂フィルムを、該樹脂の
融点よ抄低い温度で延伸することによりフィルム内部に
無機微細粉末を核として微細(r〜)ρミクロン)のミ
クロボイドが多数形成された延伸フィルムである。(Core layer) The core layer gives the synthetic paper a soft feel and has a specific surface area of 10,000 ad/f or more, preferably 15,000 ad/f or more.
A resin film containing ~500,000 cd/f of inorganic fine powder in an amount larger than the inorganic fine powder content of the surface layer (8 to 55% by weight, preferably 10 to 25% by weight) is prepared at a temperature lower than the melting point of the resin. This is a stretched film in which a large number of fine (r to ) ρ micron) microvoids are formed inside the film by stretching the film with inorganic fine powder as cores.
この中芯層は、合成紙の他の1m2(表面層、裏面層、
後述する基材層)を含め、合成紙自身の圧縮率が20〜
40%、文子ましくけ一θ〜ノρ %となるようにその
肉厚、延伸倍率、嵩密度等を決定する。This core layer covers the other 1 m2 of synthetic paper (surface layer, back layer,
The compression ratio of the synthetic paper itself, including the base material layer (described later), is 20~20.
The wall thickness, stretching ratio, bulk density, etc. are determined so that the thickness is 40% and Fumiko's weight is 1 θ to ρ %.
中芯層(6)の中に含まれる多数のミクロボイドによっ
て合成紙に圧縮性が付与される。例えば合成紙の表面に
ヘッド圧に相等する32汀/−の荷重を押しつけた時、
合成紙の厚さが20〜30%程度圧縮されうる。The large number of microvoids contained in the core layer (6) imparts compressibility to the synthetic paper. For example, when a load of 32/-, which is equivalent to the head pressure, is applied to the surface of synthetic paper,
The thickness of the synthetic paper can be compressed by about 20 to 30%.
この圧縮により、合成紙が熱転写画像用受容シートの支
持体として用いられたとき、受容シート表面層と熱転写
染料含有フィルム(熱転写リボン)との密着性が向上し
、合成紙表面層に突起物があっても、内部に押し込めら
れる結果、得られる転写画像は優れた鮮明性を有する。This compression improves the adhesion between the receiving sheet surface layer and the thermal transfer dye-containing film (thermal transfer ribbon) when the synthetic paper is used as a support for a receiving sheet for thermal transfer images, and prevents protrusions on the synthetic paper surface layer. Even if there is a transfer image, the resulting transferred image has excellent clarity as a result of being pushed inside.
(A面層)
合成紙に鉛筆筆記性を期待するときは、表面順回と反対
側に無機微細粉末を25〜65重1%含有する延伸樹脂
フィルムよりなる裏面層0を設ける。この裏面層は熱転
写時の合成紙のロールすべり性を良好とする作用も有す
る。(A-side layer) When the synthetic paper is expected to have pencil writing properties, a back layer 0 made of a stretched resin film containing 25 to 65 1% by weight of inorganic fine powder is provided on the side opposite to the front surface. This back layer also has the effect of improving the roll slipperiness of the synthetic paper during thermal transfer.
(合成紙)
本発明の合成紙は、例えば■中芯用樹脂組成物を容重押
出してフィルムを得、これをロール詳の周速差を利用し
て4〜10倍縦延伸し、ついでこの縦延伸フィルムの片
面または両面に表面層形成用樹脂組成物フィルムを溶融
ラミネート物、ついで横方向にテンターで5〜12倍横
延呻して得られる表面層(A)が−軸配向フィルム、中
芯層(B)が二軸配向フィルムであってもよいし、■こ
の三、−フィルムにおいて片方の表面層樹脂組成物を裏
面層形成用樹脂組成物にかえて表面順回と裏面層0が−
軸延沖フィルムで、中芯層63)が二軸延滞フィルムの
ものであってもよい。(Synthetic paper) The synthetic paper of the present invention can be produced by, for example, extruding the resin composition for the core by volume to obtain a film, longitudinally stretching this by 4 to 10 times using the difference in peripheral speed of the rolls, and then A surface layer (A) obtained by melt-laminating a resin composition film for forming a surface layer on one or both sides of a stretched film and then laterally stretching it 5 to 12 times in a tenter is a -axis oriented film and a core. The layer (B) may be a biaxially oriented film, or the layer (B) may be a biaxially oriented film.
In the axially stretched film, the core layer 63) may be a biaxially stretched film.
更に、■表面層形成用樹脂組成物と、中芯用形成樹脂組
成物、必要により裏面層形成用樹脂組成物を、それぞれ
別々の押出機を用いて1台の共押ダイに、)融混練供給
し、ダイ内で積層後、積層フィルムを押し出し、これを
24方向に延伸した各、イが24延伸フイルムであって
もよい。また、■無機微細粉末を3〜50重量%含有す
る樹脂縦延伸フィルム(基材層用)の少なくとも一方の
表面に、表面層形成用樹脂組成物と中芯層形成用樹脂組
成物よりなる共押出フィルムを溶融ラミネートし、つい
でこのラミネート物を横方向に延伸して表面raと中芯
層とが一軸延伸フイルムであって、基材層が二軸延伸フ
ィルムの合成紙であってもよい。さらに、■この■の合
成紙の製法において、他方の表面にラミネートされる表
面層弱形成用樹脂組成物を裏面層形成用樹脂組成物に変
えて得た表面層/中芯層/基材層/中芯層/S面層の5
層構造の合成紙であっても、■表in If1/中芯層
/基材層/裏面層の4層構造の合成紙(第2図参照)で
あってもよい。Furthermore, (1) the resin composition for forming the surface layer, the resin composition for forming the core, and if necessary the resin composition for forming the back layer are melt-kneaded into one co-extrusion die using separate extruders. After being supplied and laminated in a die, the laminated film may be extruded and stretched in 24 directions to form a 24-stretched film. In addition, on at least one surface of the longitudinally stretched resin film (for base layer) containing 3 to 50% by weight of inorganic fine powder, a copolymer comprising a resin composition for forming a surface layer and a resin composition for forming a core layer is added. The extruded film may be melt-laminated, and then this laminate is stretched in the transverse direction to form a synthetic paper in which the surface RA and the core layer are uniaxially stretched films, and the base layer is a biaxially stretched film. Furthermore, in the synthetic paper manufacturing method of ■ this ■, the surface layer/core layer/base layer obtained by changing the resin composition for weakly forming the surface layer laminated on the other surface to the resin composition for forming the back layer. /Middle core layer/S side layer 5
It may be a synthetic paper with a layered structure or a synthetic paper with a four-layer structure of (1) front in If1/core layer/base layer/back layer (see FIG. 2).
この多層構造の合成紙は中芯層として多数の延伸によっ
て生成されるミクロボイドを内部に多数含むものである
。このミクロボイドによって合成紙が熱転写画像受容シ
ートの支持体として用いられた場合、転写紙との密着性
が良好となり、とくに表面層にある突出部(凸部)が支
持体内部に押し込められるので転写の際に生ずる白抜け
が少くなる。This multilayered synthetic paper has a core layer containing a large number of microvoids produced by multiple stretching processes. When synthetic paper is used as a support for a thermal transfer image-receiving sheet, these microvoids provide good adhesion to the transfer paper, and in particular, the protrusions (convexities) on the surface layer are pushed into the support, making transfer easier. The white spots that sometimes occur are reduced.
このミクロボイド含有合成紙の内部ミクロボイドの量は
、東洋噴機■の狼傾糾りパ槌で、試料片10mX10o
+sの合成紙に200.湿度65%の条件下で160#
の荷重(面積5−)を線方向に負荷したとき、
で計算される圧縮率(JIS K−6734に準拠)
が20〜40%となる量である。The amount of internal microvoids in this microvoid-containing synthetic paper was measured using a sample piece of 10m x 10o
+s synthetic paper 200. 160# under 65% humidity condition
When a load (area 5-) is applied in the linear direction, the compression ratio is calculated as (based on JIS K-6734)
is 20 to 40%.
圧縮率が20%未満であると、熱転写印刷時に合成紙表
面の突起物が起因する色抜けの防止が困難となる。逆に
、圧縮率が40%を越えると合成紙表面に転写時のサー
マルヘッドの圧力がかからなくなり、転写リボン中の顔
料や染料が画l象受容シート知転写されない。If the compression rate is less than 20%, it will be difficult to prevent color loss caused by protrusions on the surface of the synthetic paper during thermal transfer printing. On the other hand, if the compression rate exceeds 40%, the pressure of the thermal head during transfer will not be applied to the surface of the synthetic paper, and the pigment or dye in the transfer ribbon will not be transferred to the image receiving sheet.
合成紙の肉厚は40〜SOOミクロン、好ましくは40
〜350ミクロンである。中芯層(B)は、合成紙の全
肉厚の40%以上を占める。The wall thickness of synthetic paper is 40 to SOO microns, preferably 40
~350 microns. The core layer (B) accounts for 40% or more of the total thickness of the synthetic paper.
表面層(至)の厚さは、合成紙の全厚さの10〜40%
であることが好ましい。表面層厚さが厚すぎると中芯層
の圧縮性を生かすことができず、逆に薄すぎると表面平
滑性が低下しすぎ色抜けの原因となる。The thickness of the surface layer is 10 to 40% of the total thickness of the synthetic paper.
It is preferable that If the surface layer is too thick, the compressibility of the core layer cannot be utilized, and if it is too thin, the surface smoothness is too low, causing color loss.
プロピレン系樹脂合成紙の場合の好ましい樹脂の組成を
示すと次の通りである。Preferred resin compositions for propylene resin synthetic paper are as follows.
■表面層組成:
(a)、ポリプロピレン 35〜97重量%(b)
、ポリスチレン、高密度ポリエチレン、中密度ポリエチ
レン、低密度ポリエチレン、エチレン・酢酸ビニル共重
合体より選ばれた樹脂 0〜30重け
%(C)、無機微細粉末 0〜1011%の)
中芯層組成二
(a)、ポリプロピレン 50〜9ogli%Φ)
、高密度ポリエチレン、中密度ポリエチレン、低密度ポ
リエチレン、エチレン・酢酸ビニル共重合体より選ばれ
た樹脂
O〜30重量5
(C)、無機微細粉末 10〜25重量%0裏面
層組成:
(a)、ポリプロピレン 40〜75に計%(b)
、低密度ポリエチレン、中密度ポリエチレン、高密度ポ
リエチレン、エチレン・酢酸ビニル共重合体
0〜15重量%
(C)、無機微細粉末 25〜50重量50基材
層
(a)、ポリプロピレン 60〜85重1%(b)
、ポリスチレン、高・磐度ポリエチレン、中密度ポリエ
チレン、低密度ポリエチレン、エチレン・酢酸ビニル共
重合体
3〜10重辻浄
(C)、無機微細粉末 10〜30重量%。■Surface layer composition: (a), polypropylene 35-97% by weight (b)
, polystyrene, high density polyethylene, medium density polyethylene, low density polyethylene, resin selected from ethylene/vinyl acetate copolymer 0-30% by weight (C), inorganic fine powder 0-1011%)
Core layer composition 2 (a), polypropylene 50-9ogli%Φ)
, resin selected from high-density polyethylene, medium-density polyethylene, low-density polyethylene, and ethylene/vinyl acetate copolymer O~30% by weight 5 (C), inorganic fine powder 10~25% by weight 0 Back layer composition: (a) , polypropylene 40-75% (b)
, low density polyethylene, medium density polyethylene, high density polyethylene, ethylene/vinyl acetate copolymer 0 to 15% by weight (C), inorganic fine powder 25 to 50 weight 50 base layer (a), polypropylene 60 to 85 weight 1 %(b)
, polystyrene, high-strength polyethylene, medium-density polyethylene, low-density polyethylene, 3-10 ethylene/vinyl acetate copolymer (C), inorganic fine powder 10-30% by weight.
この合成紙は、ポリプロピレンをフィルムマトリックス
樹脂とするもので、Cb)成分のポリエチレン等は延伸
性、耐衝撃性の向上に寄与するが、場剰の添加はミクロ
ボイド生成の低下につながる。This synthetic paper uses polypropylene as a film matrix resin, and component Cb) such as polyethylene contributes to improving stretchability and impact resistance, but excessive addition leads to a decrease in microvoid formation.
(c)成分の無機微細粉末の増加につれフィルム内部の
空孔数が増加し、圧縮性の向上、不透明度の向上がある
が合成紙の強度が低下する。従って、表面層中の無機微
細粉末は合成紙の表面強度を高める目的と、色抜防止の
ために平滑化する目的で中芯層の無機微細粉末含有率よ
りも少なくする。As the inorganic fine powder of component (c) increases, the number of pores inside the film increases, improving compressibility and opacity, but decreasing the strength of the synthetic paper. Therefore, the content of the inorganic fine powder in the surface layer is made smaller than the content of the inorganic fine powder in the core layer for the purpose of increasing the surface strength of the synthetic paper and smoothing the synthetic paper to prevent discoloration.
基材層0は、中芯層0でもある。従って、本発明におい
ては、中芯層と基材層の延伸軸数が異なることにより便
利的に基材層と表現したが、技術的な権利解釈としては
基材層をも中芯層として扱うべきである。The base material layer 0 is also the core layer 0. Therefore, in the present invention, the core layer and the base layer are conveniently expressed as a base layer due to the difference in the number of stretching axes, but as a technical interpretation of rights, the base layer is also treated as a core layer. Should.
(突出物)
合成紙の表面層(A)の表1■13より突出している突
出物14は、第3図に示すようにその長径2が50ミク
ロン以上のものが0.1=当抄10個以下となることが
熱転写した画像の欠けが実用上間頓とならない点で重要
である。(Protrusions) The protrusions 14 that protrude from Table 1■13 of the surface layer (A) of the synthetic paper are those whose major axis 2 is 50 microns or more as shown in Figure 3, which is 0.1 = this article 10 It is important that the number of defects be less than 100% in order to prevent defects in the thermally transferred image from becoming infrequent in practical use.
無機微細粉末は、平均粒径が10ミクロンは下であって
も、その中には粒径が15ミクロンや20 ’ミ
クロンのような粒子が少量存在した9、粒子同志複数個
凝集してその長径が50ミクロンと巨大となるものがあ
る。この巨大粒子が画像受容シート1の支持体12の表
面に有ると、この上に設けられるj面像受容層11は均
一な皮膜が形成できずひどい場合にはピンホールとなり
、これが白抜けの原因となる。Even if the average particle size of the inorganic fine powder is less than 10 microns, there are small amounts of particles with particle sizes of 15 microns or 20' microns9, and the long diameter of multiple particles aggregates. There are some that are as huge as 50 microns. If these giant particles exist on the surface of the support 12 of the image-receiving sheet 1, the J-plane image-receiving layer 11 provided thereon will not be able to form a uniform film, and in severe cases will form pinholes, which will cause white spots. becomes.
支持体12の表面順回の樹脂表面層3の平担面より突出
している突出物の高さhは、無機微細粒子の長径2より
小さい。この高さhが20ミクロン以上の突出物が0.
1m”当り5個以下であることが白抜は防止の面で好ま
しい。The height h of the protrusions protruding from the flat surface of the resin surface layer 3 on the surface of the support 12 is smaller than the major axis 2 of the inorganic fine particles. This protrusion with a height h of 20 microns or more is 0.
From the viewpoint of preventing white spots, it is preferable that the number of particles is 5 or less per 1 m''.
(画像受容シート)
本発明の合成紙12を支持体とし、この支持体上に画像
受容層11を設けることにより熱転写記録用画像受容シ
ート1が得られる。(Image-receiving sheet) The image-receiving sheet 1 for thermal transfer recording is obtained by using the synthetic paper 12 of the present invention as a support and providing the image-receiving layer 11 on this support.
画像受容層は、昇華性又は気化性染料に対して可染性を
示す樹脂、ゴム、ワックスまたはこれらと有機系ないて
無機系フィラーとの混合物が用いられる。The image-receiving layer is made of a resin, rubber, wax, or a mixture of these and an organic or inorganic filler that is dyeable with sublimable or vaporizable dyes.
樹脂、ゴム、ワックス等は、水に分散させて用いてもよ
いし、有機溶剤に溶解して用いられる。Resin, rubber, wax, etc. may be used after being dispersed in water or dissolved in an organic solvent.
樹脂、ゴム、ワックスの例として:i、例えば、アミノ
アルキッド樹す旨、ポリアミド、ポリウレタン、ポリ塩
化ビニル、ポリ酢tビニル、ポリエステル、アクリル系
樹脂、アセタール樹脂、ポリビニルアルコール、ポリ塩
化ビニリデン、ポリビニルアセタール、ポリスチレン、
ポリカーボネート、エポキシ樹脂、スチレン−ブタジェ
ンゴム(SBR)、ニトリルゴム(NBR)などのゴム
系、エチルセルロース、石油樹脂などの非水溶性の高分
子からなる接着剤単独、あるいはカルナバワックス、木
ロウなどの植物性ワックス、密ロウ、セラツカロウなど
の動物性ワックス、マイクロクリスタリンワックス、パ
ラフィンワックスなどの石油系ワックス、酸化ワックス
、エステルワックスナどの合成ワックスなどの固形ワッ
クスとを併用してなる。Examples of resins, rubbers and waxes include: i, such as amino alkyd resin, polyamide, polyurethane, polyvinyl chloride, polyvinyl acetate, polyester, acrylic resin, acetal resin, polyvinyl alcohol, polyvinylidene chloride, polyvinyl acetal ,polystyrene,
Adhesives made from rubber such as polycarbonate, epoxy resin, styrene-butadiene rubber (SBR), and nitrile rubber (NBR), water-insoluble polymers such as ethyl cellulose and petroleum resin, or vegetable-based adhesives such as carnauba wax and wood wax. It is made by using a combination of solid waxes such as animal waxes such as wax, beeswax and serratus wax, petroleum waxes such as microcrystalline wax and paraffin wax, and synthetic waxes such as oxidized waxes and ester waxes.
無機系フィラーとしては、平均粒径0.5ミクロン以下
のホワイトカーボンなどの合成シリカ、クレー、メルク
、硫酸アルミニウム、二酸化チタン、酸化亜鉛などの無
機顔料が利用でき、好ましく id平均粒径0.1μ以
下のホワイトカーボンなどの合成シリカ、軽質または重
質の炭俊カルシウムなどの無機顔料が利用できる。As the inorganic filler, synthetic silica such as white carbon with an average particle size of 0.5 microns or less, inorganic pigments such as clay, Merck, aluminum sulfate, titanium dioxide, zinc oxide, etc. can be used, preferably an id average particle size of 0.1 μm. The following synthetic silicas such as white carbon and inorganic pigments such as light or heavy calcium carbonate can be used.
有機系フィラーとしては、種々の高分子微粒子が採用さ
れるが、その粒子直径は10μm以下にするのがよい。Various fine polymer particles can be used as the organic filler, but the particle diameter is preferably 10 μm or less.
有機系フィシ−を購成する高分子としては、例えば、メ
チルセルロース、エチルセルロース、ポリスチレン、ポ
リウレタン、J素/ホルマリン樹脂、メラミン樹脂、フ
ェノール樹脂、イソ(又はジイソ)ブチレン/無水マレ
イン酸共重合体、スチレン/無水マレイン酸共重合体、
ポリ酢酸ビニル、ポリ塩化ビニル、塩化ビニル/酢酸ビ
ニル共重合体、ポリエステル、ポリアクリル酸エステル
、ポリメタクリル酸エステル、スチレン/ブタジェン/
アクリル系共重合体等が挙げられる。Examples of polymers for which organic polymers are purchased include methylcellulose, ethylcellulose, polystyrene, polyurethane, J-carbon/formalin resin, melamine resin, phenol resin, iso(or diiso)butylene/maleic anhydride copolymer, and styrene. /maleic anhydride copolymer,
Polyvinyl acetate, polyvinyl chloride, vinyl chloride/vinyl acetate copolymer, polyester, polyacrylic ester, polymethacrylic ester, styrene/butadiene/
Examples include acrylic copolymers.
これらフィラーは通常30重量%以下の割合で夏用され
る。特に無機系フィラーはその表面をロート油、ドデシ
ル硫酸ナトリウム、有機アミン、金属セッケンリグニン
スルホン酸ナトリウムなどの非イオン、陽イオン、両性
活性剤で処理することにより、転写紙2のインクとの濡
れが良化され好適に使用できる。These fillers are usually used in summer at a proportion of 30% by weight or less. In particular, inorganic fillers can be treated with nonionic, cationic, or amphoteric activators such as funnel oil, sodium dodecyl sulfate, organic amines, and sodium metal soap ligninsulfonate to prevent wetting of the transfer paper 2 with the ink. It has been improved and can be used suitably.
画像受容層11は、前記支持体12の表面層(ト)側に
塗工、乾燥され形成される。塗工には、プレー)”=r
−p、エアーす(フコータ、ロールコータ、バーコータ
などの通常の塗工機、あるいはサイズプレス、ゲートロ
ール装置などを用いる。The image-receiving layer 11 is formed by coating and drying the surface layer (g) side of the support 12. For coating, play)”=r
-p, air coater (use a regular coating machine such as a coater, roll coater, bar coater, size press, gate roll device, etc.).
画像受容層11の肉厚は0.5〜20ミクロン、好まし
くは3〜15ミクロンである。塗工、乾燥後、画像受容
シートに平滑性を付与するためにスーパーカルダンを用
いて圧縮し、シートの平滑度をA整してもよい。The thickness of the image-receiving layer 11 is between 0.5 and 20 microns, preferably between 3 and 15 microns. After coating and drying, the image-receiving sheet may be compressed using supercardan to give it smoothness, and the smoothness of the sheet may be adjusted to A.
合成紙の製造例
実施例1
(1)メルトインデックス(MI)0.8のポリプロピ
レン79重量%、高密度ポリエチレン5重量%の混合物
に比表面積15,000ad/fの炭酸カルシウム16
重量%を配合a3)し、270℃に設定した押出機にて
混練後、シート状に押出し、冷却装置により冷却して、
無延伸シートを得た。このシートを、140℃に加熱後
、縦方向に5倍延伸した。Production Example of Synthetic Paper Example 1 (1) Calcium carbonate 16 with a specific surface area of 15,000 ad/f is added to a mixture of 79% by weight of polypropylene with a melt index (MI) of 0.8 and 5% by weight of high-density polyethylene.
% by weight a3), kneaded in an extruder set at 270°C, extruded into a sheet, cooled with a cooling device,
A non-stretched sheet was obtained. This sheet was heated to 140°C and then stretched 5 times in the machine direction.
+21MI4.(C)のポリプロピレン95重量%に、
平均粒径1.5μ、比表面積15,000 f/?ri
″の炭酸カルシウム5重量%を混合した組成物(A)を
押出機で溶融混練し、押出したシートを(1)の5倍延
伸シートの片面に積層し、(1)の5培延呻シートの反
対面にMI4.(C)のポリプロピレン55重量%に平
均粒径1.5μ、比表面積が15.0OOi/fの炭酸
カルシウム45重量%を混合した組成物(Qを別の押出
機で溶強混練し、押出積層し、ついで60℃tで冷却後
、162℃まで加熱し、テンターで横方向に7.5倍延
伸し、165℃でアニーリング処理し、60℃まで冷却
し、耳部をスリットして3層(A/B/C肉厚10/7
0/30ミクロン)構造の合成紙を得た。+21MI4. (C) 95% by weight of polypropylene,
Average particle size 1.5μ, specific surface area 15,000 f/? ri
Composition (A) mixed with 5% by weight of calcium carbonate is melt-kneaded in an extruder, and the extruded sheet is laminated on one side of the 5-fold stretched sheet of (1) to form the 5-fold stretched sheet of (1). On the other side of Strongly kneaded, extruded and laminated, then cooled at 60°C, heated to 162°C, stretched 7.5 times in the transverse direction with a tenter, annealed at 165°C, cooled to 60°C, and removed the edges. Slit and 3 layers (A/B/C wall thickness 10/7
A synthetic paper with a structure of 0/30 micron) was obtained.
この合成紙の表面(A)のベック指数は5,800秒で
あり、不透変が95.6%で、圧縮率は25%であった
。The Beck index of the surface (A) of this synthetic paper was 5,800 seconds, the opacity was 95.6%, and the compression rate was 25%.
また、表面層(ト)の樹脂表面層3より突出している突
出物の長径βが50ミクロン以上の突起個数は0.1m
”当り4個であり、高さ20ミクロン以上のものは0.
1m2当妙1個であった。In addition, the number of protrusions that protrude from the resin surface layer 3 of the surface layer (G) and have a longer diameter β of 50 microns or more is 0.1 m.
4 pieces per unit, and 0.0 pieces for items over 20 microns in height.
There was one piece per 1m2.
実施例2
(1) メルトインデックス(MI)0.8のポリプ
ロピレン79重量%、高密度ポリエチレン5重量%の混
合物に比表面積15.Q 00c!I/fの炭酸カルシ
ウム16重量%を配合(B)し、270℃に設定した押
出機にて混練後、シート状に押出し、冷却装置によ秩冷
却して、無延伸シートを得た。このシートを、140℃
に加熱後、縦方向に5倍延伸した。Example 2 (1) A mixture of 79% by weight of polypropylene with a melt index (MI) of 0.8 and 5% by weight of high-density polyethylene has a specific surface area of 15. Q 00c! 16% by weight of calcium carbonate of I/f was blended (B), kneaded in an extruder set at 270°C, extruded into a sheet, and cooled in a cooling device to obtain a non-stretched sheet. This sheet was heated to 140℃.
After heating, the film was stretched 5 times in the longitudinal direction.
(A1MI4.0り710分のポリプロピレン97.5
重役%に比表面積25.000 cfI/りの硫酸バリ
ウム2.5重量%を混合した組成物(A)を押出機で溶
融混練し、押出したシートを(1)の5倍延伸シートの
片面に積層し、(1)の5倍延伸シートの反対面にMI
4.(C)のポリプロピレン55重量うに比表面積がi
s、o o ocra7tの炭酸カルシウム45直量
%を混合した組成物C)を別の押出機で溶融混練し、押
出積層しついで60℃まで冷却後、162℃まで加熱し
、テンターで横方向に7.5倍延伸1..165℃でア
ニーリング処理し、60′cまで冷却し、耳部をスリッ
トして3層(A/B/C;肉厚10/70/30iクロ
ン)構造の合成紙を得たつこの合成紙の表面(A)のベ
ック指数は5.500秒であり、不透明度が96.5%
で圧縮率は23%であった。(A1MI4.0ri710min polypropylene 97.5
Composition (A), in which 2.5% by weight of barium sulfate with a specific surface area of 25.000 cfI/liter was mixed with % of heavy duty, was melt-kneaded in an extruder, and the extruded sheet was placed on one side of the 5-fold stretched sheet of (1). Laminated and MI on the opposite side of the 5 times stretched sheet of (1)
4. The specific surface area of the polypropylene 55 (C) by weight is i
Composition C), which is a mixture of 45% by volume of calcium carbonate of 7t of ocra, was melt-kneaded in another extruder, extrusion laminated, cooled to 60°C, heated to 162°C, and transversely mixed with a tenter. 7.5 times stretching 1. .. The surface of this synthetic paper was annealed at 165°C, cooled to 60'c, and the edges were slit to obtain a synthetic paper with a three-layer (A/B/C; wall thickness 10/70/30cm) structure. The Beck index of (A) is 5.500 seconds and the opacity is 96.5%.
The compression ratio was 23%.
また、表面層(至)の樹脂表面層3より突出している突
出物の長径ぶが50ミクロン以上の突起個数は0.1
m’当り7個であり、高さ20ミクロン以上のものは0
.1m”当り2個であった。In addition, the number of protrusions with a long diameter of 50 microns or more that protrudes from the resin surface layer 3 of the surface layer (end) is 0.1
7 pieces per m', and 0 for those with a height of 20 microns or more.
.. There were 2 pieces per 1 m''.
実施例3
表面l(A)の組成物として、ポリプロピレン981寸
%と比表面積が30.000 crl/ ?のTiO2
2重量−70との混合′吻を用いる・池は実施例1と同
様にして表1に示す物性の合成紙を得た。Example 3 The composition of surface l(A) is 981% polypropylene and a specific surface area of 30.000 crl/? of TiO2
Synthetic paper having the physical properties shown in Table 1 was obtained in the same manner as in Example 1 using a mixture with 2-70% by weight.
実施例4
ダイのスリット幅を変更する池は実施列lと同様にして
肉厚がA/B/C: 5/70/1 sミクロンの31
層構造の合成紙を得た。Example 4 The pond for changing the die slit width was made in the same way as in the implementation row 1, and the wall thickness was A/B/C: 5/70/1 s micron 31
A synthetic paper with a layered structure was obtained.
実・布fI5
(1)メルトインデックス(MI)0.8のポリプロビ
レ2フ9重量%、高密度ポリエチレン5重債%の混合物
に比表面積15,000IJl/Pの炭酸カルシウム2
5重量%を配合0)し、270℃に設定した押出機にて
混線後、シート状に押出し、冷却装置により冷却して、
無延伸シートを得た。このシートを、140℃に加熱後
、縦方向に5倍延伸した。Fruit/cloth fI5 (1) Calcium carbonate 2 with a specific surface area of 15,000 IJl/P in a mixture of 9% by weight of polypropylene 2 with a melt index (MI) of 0.8 and 5% with high density polyethylene.
5% by weight (0) was mixed in an extruder set at 270°C, extruded into a sheet, cooled with a cooling device,
A non-stretched sheet was obtained. This sheet was heated to 140°C and then stretched 5 times in the machine direction.
+21MIが4.(C)のポリプロピレン(3)と、I
V114.(C)のポリプロビレ255重量%に比表面
積が1s、o o ocrli/ yの炭酸カルシウム
40fiffi%を混合した組成物(B)を別々の押出
機で溶融混練し、ダイ内で積層し、シート状に共押出し
、(1)の5倍延伸シートの両面(表面は囚が外1萌に
なるように裏面は[F])が外側になる様に)積層し、
ついで60℃まで冷却後、162℃まで加熱し、テンタ
ーで横方向に7.5倍延伸し、165℃でアニーリング
処理した後、60℃まで冷却し、耳部をスリットして、
5層構造(A/B/D、/A/B :肉厚5/15/6
0/1515ミクロン)の合成紙を得た。+21 MI is 4. (C) polypropylene (3) and I
V114. Composition (B), which is a mixture of 255% by weight of polypropylene (C) and 40fiffi% of calcium carbonate with a specific surface area of 1 s and o o crli/y, is melt-kneaded in a separate extruder, laminated in a die, and formed into a sheet. Co-extruded and laminated both sides of the 5 times stretched sheet of (1) so that the front side is on the outside and [F] on the back side is on the outside).
Then, after cooling to 60°C, heating to 162°C, stretching 7.5 times in the transverse direction with a tenter, annealing at 165°C, cooling to 60°C, and slitting the edges.
5-layer structure (A/B/D, /A/B: wall thickness 5/15/6
A synthetic paper of 0/1515 micron) was obtained.
比較例1
表面層(A)の組成物として比表面積がs、oooc1
1/fの炭酸カルシウム5重量%とM I 4.(C)
のポリプロピレン95重量%の混合物を用いる他は例1
と同様例して表1に示す物性の合成紙を得た。Comparative Example 1 The composition of the surface layer (A) has a specific surface area of s, oooc1
1/f calcium carbonate 5% by weight and M I 4. (C)
Example 1 except that a mixture of 95% by weight of polypropylene was used.
A synthetic paper having the physical properties shown in Table 1 was obtained in the same manner as above.
比較例2
実施例1において、ダイのスリット幅を変更する他は例
1と同様にして表1に示す物性の合成紙を得た。Comparative Example 2 A synthetic paper having the physical properties shown in Table 1 was obtained in the same manner as in Example 1 except that the slit width of the die was changed.
比較例3
(1) メルトインデックス(M I ) 0.8の
ポリプロピレン90重量%、高密度ポリエチレン5重景
%の混合物に比表面積15,000 cl/ tの炭酸
カルシウム5重量%を配合(6)し、270℃に設定し
た押出機にて混線後、シート状に押出し、冷却装置によ
り冷却して、無延伸シートを得た。このシートを、14
0℃に加熱後、縦方向に5倍延伸した。Comparative Example 3 (1) 5% by weight of calcium carbonate with a specific surface area of 15,000 cl/t was blended into a mixture of 90% by weight of polypropylene with a melt index (MI) of 0.8 and 5% by weight of high-density polyethylene (6) After mixing in an extruder set at 270° C., the mixture was extruded into a sheet and cooled with a cooling device to obtain a non-stretched sheet. This sheet, 14
After heating to 0°C, it was stretched 5 times in the machine direction.
(A1M I 4.(C)のポリプロピレン95重量%
に比表面積15,000 f / m”の炭酸カルシウ
ム5重量%を混合した組成物■を押出機で溶I触混線し
、押出したシートを(1)の5倍延伸シートの片面にf
f1層し、(1)の5倍延伸シートの反対面にMI4.
(C)のポリプロピレン55重1%に比表面積が15.
000atl/fの炭酸カルシウム45 MfJ%を混
合した組成物0を別の押出機で溶融混練し、押出積層し
、ついで60℃まで冷却後、162℃まで、17alo
し、テンターで横方向に7.5倍延伸し、165℃でア
ニーリング処理し、60℃まで冷却し、耳部をスリット
して3層(B/A/C;肉厚10/70/30ミクロン
)構造の合成紙を得た。(A1M I 4. (C) 95% by weight of polypropylene
A mixture of 5 wt.
f1 layer, and MI4.
(C) Polypropylene 55% by weight has a specific surface area of 15.
Composition 0 mixed with 45 MfJ% of calcium carbonate at 000 atl/f was melt-kneaded in another extruder, extrusion laminated, cooled to 60°C, and heated to 162°C to 17alo
It was stretched 7.5 times in the transverse direction using a tenter, annealed at 165°C, cooled to 60°C, and the edges were slit to form 3 layers (B/A/C; wall thickness 10/70/30 microns). ) structure synthetic paper was obtained.
この合成、祇の表面■のペック指数ば7.’500秒で
あり、不透明度が90.5%で圧縮ぷは15%であった
。In this synthesis, the Peck index of the surface ■ is 7. '500 seconds, opacity was 90.5% and compression was 15%.
また、表面層Aの對脂表面層3より突出している突出物
の長径2が50ミクロンμ上の突起個数は0.1m”当
り8個であり、高さ20ミクロン以上のものは0.1m
2当や1個であった。In addition, the number of protrusions with a long diameter 2 of 50 microns μ that protrudes from the resinous surface layer 3 of the surface layer A is 8 per 0.1 m, and those with a height of 20 microns or more are 0.1 m.
It was 2 or 1.
比較例4
(1) メルトインデックス(〜II)0.8.)ポ
リプロビレン79重量%、高密度ポリエチレン5重量%
の混合物に比表面積が15,000aA/lの炭酸カル
シウム16重量%を配合(均し、270℃に設定した押
出様にて混線後、シート状に押出し、冷却装置1/(よ
し冷却して、無延伸シートを得た。このシートを、14
0℃に加熱後、縦方向に5倍延伸した。Comparative Example 4 (1) Melt index (~II) 0.8. ) 79% by weight of polypropylene, 5% by weight of high-density polyethylene
Add 16% by weight of calcium carbonate with a specific surface area of 15,000 aA/l to the mixture of A non-stretched sheet was obtained.This sheet was
After heating to 0°C, it was stretched 5 times in the machine direction.
(A1MI4.oのポリプロピレン55重1%に比表面
積ls、o o oal/yの炭酸カルシウム45重量
%を混合した組成物(Oを押出機で@融混練し、押出し
たシートを(1)の5倍延伸シートの両面に積層し、つ
いで60′C′1で冷却後、162℃まで加熱し、テン
ターで横方向に7.5倍延伸し、165℃でアニーリン
グ処理し、60℃まで冷却し、耳部をスリットして3:
漫(C/B/C:肉厚10/70/30ミクロン)構造
の合成紙を得た。(A composition in which 55% by weight of polypropylene of A1MI4.o was mixed with 45% by weight of calcium carbonate of specific surface area ls, o o oal/y (O was melt-kneaded in an extruder, and the extruded sheet was mixed with (1) Laminated on both sides of a 5x stretched sheet, then cooled at 60'C'1, heated to 162°C, stretched 7.5x in the transverse direction with a tenter, annealed at 165°C, cooled to 60°C. , slit the ears and 3:
A synthetic paper with a circular (C/B/C: wall thickness of 10/70/30 microns) structure was obtained.
この合成紙の表面(Qのベック指数は500秒でち9、
不透明度が96.0%であり圧縮率は18%であった。The surface of this synthetic paper (the Beck index of Q is 500 seconds, 9,
The opacity was 96.0% and the compression rate was 18%.
また、表面層の樹脂表面層3より突出している突出物の
長径2が50ミクロン以上の突起個数は0.1m2当り
15個であり、高さ20ミクロン以上のものは0.1m
2当り6個であった。In addition, the number of protrusions with a long diameter 2 of 50 microns or more that protrudes from the resin surface layer 3 of the surface layer is 15 per 0.1 m2, and those with a height of 20 microns or more are 0.1 m2.
There were 6 pieces per 2 pieces.
比較例5
(1)メルトインデックス(MI)0.8のポリプロピ
レン60重量%、高密度ポリエチレン5重量%の混合物
に比表面積が15,000cd/fの炭酸カルシウム3
5重量%を配合(6)し、270℃に設定した押出機に
て混線後、シート状に押出し、冷却装置により冷却して
、無延伸シートを得た。このシートを、140℃に加熱
後、縦方向に5@延伸した。Comparative Example 5 (1) Calcium carbonate 3 with a specific surface area of 15,000 cd/f was added to a mixture of 60% by weight of polypropylene with a melt index (MI) of 0.8 and 5% by weight of high-density polyethylene.
5% by weight was blended (6), mixed in an extruder set at 270°C, extruded into a sheet, and cooled with a cooling device to obtain a non-stretched sheet. This sheet was heated to 140° C. and then stretched for 5 times in the longitudinal direction.
(A)MIa、oのポリプロピレン95重量%に比表面
積が15,000d/ ?の炭酸カルシウム5重量%を
混合した組成物代を押出機で溶融混練し、押出したシー
トを(1)の5倍延伸シートの両面に積層し、ついで6
0℃まで冷却後、162℃まで加熱し、テンターで横方
向に7.5倍延伸し、165℃でアニーりング処理し、
60′cまで冷却し、耳部をスリットして31藷(A/
B/A:肉厚10/70、/30ミクロン)構造の合成
紙を得た。(A) MIa,o polypropylene 95% by weight has a specific surface area of 15,000d/? A composition containing 5% by weight of calcium carbonate was melt-kneaded in an extruder, and the extruded sheet was laminated on both sides of the 5-fold stretched sheet of (1).
After cooling to 0°C, it was heated to 162°C, stretched 7.5 times in the transverse direction with a tenter, and annealed at 165°C.
Cool to 60'c, slit the ears and make 31cm (A/
B/A: Synthetic paper having a wall thickness of 10/70, /30 microns) was obtained.
この合成紙のベック指数は12.000秒であり、支持
体としての不透明度が97.5%で圧縮度は4.2%で
あった。The Beck index of this synthetic paper was 12.000 seconds, the opacity as a support was 97.5%, and the degree of compression was 4.2%.
まだ、表面順回の樹脂表面層3より突出している突出物
の長径2がSOミクロン以上の突起個数は0.1m’当
り8個であり、高さ20ミクロン以上のものけ0.1m
2当り5個であった。However, the number of protrusions with a long diameter 2 of SO microns or more that protrudes from the resin surface layer 3 on the surface is 8 per 0.1 m', and only 0.1 m with a height of 20 microns or more.
There were 5 pieces per 2 pieces.
なお、突出物の突出個数の測定は次の方法で行った。Note that the number of protrusions was measured by the following method.
+1)20α×25αに断裁した合成紙試料の表面に斜
光線をあて、突出部分を目視で捜しマークをつける。+1) Shine an oblique light beam onto the surface of a synthetic paper sample cut to 20α×25α, visually search for protruding parts, and mark them.
(A)マークがつけられた突出部分を、倍率25倍に設
定した実体顕微鏡で現察し、PEAKスケールルーぺの
ノに2スケールテ測定シ、長径が50μm以上のものの
個数を数える。(A) Observe the marked protrusions using a stereomicroscope set to 25x magnification, and count the number of protrusions with a major axis of 50 μm or more using a PEAK scale loupe.
(3) これを2枚の試料について行い、合計個数を
0.1yn”当りの突起(A)数(径)とする。(3) Do this for two samples, and let the total number be the number (diameter) of protrusions (A) per 0.1yn''.
(A) この突起部を全数■小板研究所製三次元粗さ
解析装置Model 5PA−11(商品名)で測定し
、高さが20重以上のものを0.1 m’当りの突起個
数(高)とする。(A) All of these protrusions were measured using a three-dimensional roughness analyzer Model 5PA-11 (product name) manufactured by Koita Research Institute, and the number of protrusions per 0.1 m' was measured for those with a height of 20 or more. (high).
また、合成紙の平担面18とは、第3図、第4図に示し
たような突出物14について、その頂点から該突出物の
長径(1)方向に2■離れた合成紙表面0上の点16−
a、16−bを中心にして突出物の長径(A)に垂直な
4簡の線分16.16’を描き、この線分16.16’
上を安立電気■製連続厚み計ELECTRONICMI
CROMETERK−306A(商品名)で測定し、こ
の線分上16.16’の一番高い点17.17’を求め
、一方、突出物の頂点α9より長径(1)に垂直方向に
合成紙表面0上に21離れた点16−c、16−dを中
心に長径ぷに平行な41の、線分16“、16“′を描
き、この線分16“、16′″上を上記厚み計で測定し
、この線分上16“、16″の一番高い点17“、17
N′を求め、この17.17′、17“、17″′より
高い順に3点を選び、この3点を含む平面を平担面18
とする(第5図では、17.17′、17“を結ぶ面)
。Furthermore, the flat surface 18 of the synthetic paper refers to the surface 0 of the synthetic paper 2 cm away from the apex of the protrusion 14 as shown in FIGS. 3 and 4 in the direction of the major axis (1) of the protrusion. Upper point 16-
Draw a four-strip line segment 16.16' perpendicular to the major axis (A) of the protrusion, centering on a and 16-b, and draw this line segment 16.16'.
Continuous thickness gauge ELECTRONICMI made by Anritsu Electric ■
Measure with CROMETERK-306A (trade name) to find the highest point 17.17' of 16.16' on this line, and on the other hand, measure the surface of the synthetic paper in the direction perpendicular to the major axis (1) from the apex α9 of the protrusion. Draw 41 line segments 16", 16"' parallel to the major axis centering on points 16-c, 16-d 21 apart on 0, and use the thickness gauge above to draw 41 line segments 16", 16"' on these line segments 16", 16"". Measure and find the highest point 17", 17 on this line segment 16", 16"
Find N', select three points in order higher than 17.17', 17", 17"', and define the plane containing these three points as the flat surface 18.
(In Figure 5, the plane connecting 17, 17' and 17")
.
但し、連続厚み計で各線分16.16’、16“、16
″上を測定した頂点(17,17′、17“、17//
)と同一線上で測定した最低点の差が10μm以上あ
る場合は新たに該線分の16−a、16−b。However, each line segment is 16.16', 16", 16 with a continuous thickness gauge.
Vertex measured above (17, 17', 17", 17//
) and the lowest point measured on the same line is 10 μm or more, new line segments 16-a and 16-b.
16−c、16−dの近傍に新たに中心点16−a、
16−bXl 6−cもしくは16−dを設けて同様
の手順により平担面18を求める。New center points 16-a and 16-d are added near 16-c and 16-d.
16-bXl 6-c or 16-d is provided and a flat surface 18 is obtained by the same procedure.
これら実施例1〜5、比較例1〜5で得た合成紙の物性
を表1に示す。Table 1 shows the physical properties of the synthetic papers obtained in Examples 1 to 5 and Comparative Examples 1 to 5.
なお、熱転写用画像受容シートとしての評価は次の方法
知よる。The evaluation as an image-receiving sheet for thermal transfer is based on the following method.
合成紙の表面層(A)側に下記組成の塗工剤を固型分で
約105’/m″となるように塗工し、乾燥して支持体
上に画像受容層(肉厚約10ミクロン)を設けた画像受
容シートを得た。A coating agent having the following composition is applied to the surface layer (A) side of the synthetic paper to a solid content of approximately 105'/m'', and dried to form an image-receiving layer (thickness approximately 10 An image-receiving sheet provided with microns) was obtained.
(a)ポリエステル樹脂エマルジョン 40g(樹
脂濃度50%)
(′b)炭酸カルシウム 20部
(c)水 40部。(a) Polyester resin emulsion 40g (resin concentration 50%) ('b) Calcium carbonate 20 parts (c) Water 40 parts.
この熱転写用画像受容シートを次の方法で評価した。結
果を表1に示す。This image-receiving sheet for thermal transfer was evaluated by the following method. The results are shown in Table 1.
画像の判定方法:
(1)作成した画像受容シートと昇華性染料(商品名、
Kayaset Bluee 136.日本化薬類)を
塗布乾燥した転写紙を重ね合せ、120℃で5秒間加熱
し画像を得るう
(A)得られた画像の濃度と白抜は程度を下記の5段階
で評価した。Image judgment method: (1) Prepared image receiving sheet and sublimable dye (trade name,
Kayaset Blue 136. Transfer papers coated with Nippon Kayakuryu (Nippon Kayakuryu) and dried were stacked and heated at 120° C. for 5 seconds to obtain an image. (A) The density and whiteness of the obtained image were evaluated on the following five scales.
評価基準
5 大変良い
4 良い
3 実用上支障は無い
2 実用上問題有る
1 悪い
耐ブロッキング性の試験二
30c!!lX30mの試料の表と裏を合わせ、温度4
0℃、湿度60%の4囲気中で5002の荷重を加えた
状態で24時間放置した。Evaluation criteria 5: Very good 4 Good 3 No practical problems 2 Practical problems 1 Poor blocking resistance test 2 30c! ! Put the front and back sides of the 1×30m sample together and heat to 4.
It was left for 24 hours under a load of 5002 in a four-wall environment at 0° C. and 60% humidity.
JIS K−6833に準じ、次の基準で判定を行な
った。Judgment was made based on the following criteria according to JIS K-6833.
× 表面に損傷を認める程度のブロッキング。× Blocking to the extent that damage is observed on the surface.
○ 容易に試料が引きはがれる。○ The sample is easily peeled off.
(以下余白)(Margin below)
第1図は、転写感熱記録装置の平面図、第2図は合成紙
の断面図、第3図は合成紙の部分断面図、第4図は合成
紙の平担面を決定する方法を示す部分斜視図である。
図中、1は熱転写記録用画像受容シート、11は画像受
容層、12は合成紙、2は転写体、14は突出物、Aは
表面層、Bは中芯層、Cは裏面層である。
特許出願人 王子油化合成紙株式会社
代理人 弁理士 長 谷 正 久
代理人 弁理士 山 本 隆 也
第1図
第3図
第4図Fig. 1 is a plan view of a transfer thermal recording device, Fig. 2 is a sectional view of synthetic paper, Fig. 3 is a partial sectional view of synthetic paper, and Fig. 4 shows a method for determining the flat surface of synthetic paper. FIG. In the figure, 1 is an image-receiving sheet for thermal transfer recording, 11 is an image-receiving layer, 12 is a synthetic paper, 2 is a transfer body, 14 is a protrusion, A is a surface layer, B is a core layer, and C is a back layer. . Patent applicant: Oji Yuka Synthetic Paper Co., Ltd. Agent: Masahisa Hase Patent attorney: Takashi Yamamoto, patent attorney Figure 1 Figure 3 Figure 4
Claims (1)
熱可塑性樹脂フィルムの表面層と、(B)比表面積が1
0,000cm^2/g以上の無機微細粉末を表面層の
無機微細粉末の含有量より多く含むミクロボイドを多数
含有する延伸樹脂フィルム中芯層を少なくとも含有する
2層以上の合成紙であつて、該合成紙は、 (イ)、圧縮率が20〜40%であつて、かつ、(ロ)
、前記表面層(A)は、その平担面より突出した突出物
の最長長さが50ミクロン以 上のものが0.1m^2当り10個以下であることを特
徴とする複層構造の合成紙。 2)、(A)、無機微細粉末を0〜25重量%含有する
熱可塑性樹脂フィルムの表面層と、(B)比表面積が1
0,000cm^2/g以上の無機微細粉末を表面層の
無機微細粉末の含有量より多く含むミクロボイドを多数
含有する延伸樹脂フィルム中芯層と、(C)無機微細粉
末を25〜65重量%含有する延伸樹脂フィルムよりな
る裏面層を少なくとも含有する3層以上の合成紙であつ
て、該合成紙は、 (イ)、圧縮率が20〜40%であつて、かつ、(ロ)
、前記表面層(A)は、その平担面より突出した突出物
の最長長さが50ミクロン以 上のものが0.1m^2当り10個以下であることを特
徴とする複層構造の合成紙。 3)、中芯層(B)と表面層(A)が1軸方向又は2軸
方向に延伸されて得られた配向フィルムであることを特
徴とする特許請求の範囲第1項又は第2項記載の合成紙
。 4)、表面層(A)が一軸方向に配向した延伸フィルム
であり、中芯層(B)が二軸方向に配向した延伸フィル
ムであることを特徴とする特許請求の範囲第1項記載ま
たは第2項記載の合成紙。 5)、表面層(A)の肉厚が1〜15ミクロンであり、
中芯層(B)の肉厚が全厚さの40%以上であることを
特徴とする特許請求の範囲第3項記載の合成紙。 6)、表面層(A)の肉厚が1〜15ミクロンであり、
中芯層(B)の肉厚が全厚さの40%以上であることを
特徴とする特許請求の範囲第4項記載の合成紙。 7)、表面層(A)の肉厚が1〜15ミクロンであり、
裏面層(C)の肉厚が1〜35ミクロンであることを特
徴とする特許請求の範囲第2項記載の合成紙。 8)、表面層(A)の無機微細粉末含量が0〜10重量
%、中芯層(B)の無機微細粉末含量が10〜25重量
%、裏面層(C)の無機微細粉末含量が25〜50重量
%であることを特徴とする特許請求の範囲第2項記載の
合成紙。[Claims] 1) (A) a surface layer of a thermoplastic resin film containing 0 to 25% by weight of inorganic fine powder, and (B) a specific surface area of 1.
A synthetic paper with two or more layers including at least a stretched resin film core layer containing a large number of microvoids containing inorganic fine powder of 0,000 cm^2/g or more than the content of inorganic fine powder in the surface layer, The synthetic paper has (a) a compression ratio of 20 to 40%, and (b)
, wherein the surface layer (A) has a multilayer structure in which the number of protrusions protruding from the flat surface with a longest length of 50 microns or more is 10 or less per 0.1 m^2. paper. 2) (A) a surface layer of a thermoplastic resin film containing 0 to 25% by weight of inorganic fine powder; and (B) a surface layer with a specific surface area of 1
A stretched resin film core layer containing a large number of microvoids containing 0,000 cm^2/g or more of inorganic fine powder than the content of inorganic fine powder in the surface layer, and (C) 25 to 65% by weight of inorganic fine powder. A synthetic paper with three or more layers including at least a back layer made of a stretched resin film, which (a) has a compression ratio of 20 to 40%, and (b)
, wherein the surface layer (A) has a multilayer structure in which the number of protrusions protruding from the flat surface with a longest length of 50 microns or more is 10 or less per 0.1 m^2. paper. 3) Claims 1 or 2, characterized in that the core layer (B) and the surface layer (A) are oriented films obtained by stretching in one or two directions. Synthetic paper as described. 4), the surface layer (A) is a stretched film oriented in a uniaxial direction, and the core layer (B) is a stretched film oriented in a biaxial direction, or Synthetic paper according to item 2. 5), the thickness of the surface layer (A) is 1 to 15 microns,
4. The synthetic paper according to claim 3, wherein the thickness of the core layer (B) is 40% or more of the total thickness. 6), the thickness of the surface layer (A) is 1 to 15 microns,
5. The synthetic paper according to claim 4, wherein the thickness of the core layer (B) is 40% or more of the total thickness. 7), the thickness of the surface layer (A) is 1 to 15 microns,
3. The synthetic paper according to claim 2, wherein the back layer (C) has a wall thickness of 1 to 35 microns. 8) The content of inorganic fine powder in the surface layer (A) is 0 to 10% by weight, the content of inorganic fine powder in the core layer (B) is 10 to 25% by weight, and the content of inorganic fine powder in the back layer (C) is 25% by weight. The synthetic paper according to claim 2, characterized in that the content is 50% by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61079442A JPS62259848A (en) | 1986-04-07 | 1986-04-07 | Synthetic paper having double layer structure |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61079442A JPS62259848A (en) | 1986-04-07 | 1986-04-07 | Synthetic paper having double layer structure |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62259848A true JPS62259848A (en) | 1987-11-12 |
JPH043904B2 JPH043904B2 (en) | 1992-01-24 |
Family
ID=13689992
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61079442A Granted JPS62259848A (en) | 1986-04-07 | 1986-04-07 | Synthetic paper having double layer structure |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62259848A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01130989A (en) * | 1987-11-18 | 1989-05-23 | Matsushita Electric Ind Co Ltd | Image acceptor for thermosensitive transfer |
JPH01280586A (en) * | 1988-05-06 | 1989-11-10 | Mitsubishi Kasei Corp | Image-receiving paper for thermal transfer |
JPH021381A (en) * | 1988-05-20 | 1990-01-05 | Matsushita Electric Ind Co Ltd | Thermal sublimation type transfer recording paper, production thereof, packaging method therefor and paper-supplying cassette |
JPH0226739A (en) * | 1988-07-18 | 1990-01-29 | Toray Ind Inc | Composite film and printing base material for printer |
JPH04101891A (en) * | 1989-12-11 | 1992-04-03 | Eastman Kodak Co | Heat dyestuff transfer redeiving body coated with blended polyethylene/ polypropylene |
JPH04123300U (en) * | 1991-04-12 | 1992-11-06 | 十條製紙株式会社 | Laminated waterproof sheet for single-sided offset printing |
JPH11510121A (en) * | 1995-12-15 | 1999-09-07 | ピーピージー・インダストリーズ・インコーポレイテッド | Print sheet |
-
1986
- 1986-04-07 JP JP61079442A patent/JPS62259848A/en active Granted
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01130989A (en) * | 1987-11-18 | 1989-05-23 | Matsushita Electric Ind Co Ltd | Image acceptor for thermosensitive transfer |
JPH01280586A (en) * | 1988-05-06 | 1989-11-10 | Mitsubishi Kasei Corp | Image-receiving paper for thermal transfer |
JPH021381A (en) * | 1988-05-20 | 1990-01-05 | Matsushita Electric Ind Co Ltd | Thermal sublimation type transfer recording paper, production thereof, packaging method therefor and paper-supplying cassette |
JPH0226739A (en) * | 1988-07-18 | 1990-01-29 | Toray Ind Inc | Composite film and printing base material for printer |
JPH0696281B2 (en) * | 1988-07-18 | 1994-11-30 | 東レ株式会社 | Printing base for composite film and printer |
JPH04101891A (en) * | 1989-12-11 | 1992-04-03 | Eastman Kodak Co | Heat dyestuff transfer redeiving body coated with blended polyethylene/ polypropylene |
JPH04123300U (en) * | 1991-04-12 | 1992-11-06 | 十條製紙株式会社 | Laminated waterproof sheet for single-sided offset printing |
JPH11510121A (en) * | 1995-12-15 | 1999-09-07 | ピーピージー・インダストリーズ・インコーポレイテッド | Print sheet |
Also Published As
Publication number | Publication date |
---|---|
JPH043904B2 (en) | 1992-01-24 |
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