JPS62218180A - Ink jet recording sheet - Google Patents
Ink jet recording sheetInfo
- Publication number
- JPS62218180A JPS62218180A JP6075186A JP6075186A JPS62218180A JP S62218180 A JPS62218180 A JP S62218180A JP 6075186 A JP6075186 A JP 6075186A JP 6075186 A JP6075186 A JP 6075186A JP S62218180 A JPS62218180 A JP S62218180A
- Authority
- JP
- Japan
- Prior art keywords
- ink
- water
- receiving layer
- gelatine
- gelatin
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 229920000159 gelatin Polymers 0.000 claims abstract description 29
- 235000019322 gelatine Nutrition 0.000 claims abstract description 29
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 13
- 230000008961 swelling Effects 0.000 claims abstract description 4
- 108010010803 Gelatin Proteins 0.000 claims description 24
- 239000008273 gelatin Substances 0.000 claims description 24
- 235000011852 gelatine desserts Nutrition 0.000 claims description 24
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract description 5
- 229920002472 Starch Polymers 0.000 abstract description 5
- 235000019698 starch Nutrition 0.000 abstract description 5
- 239000000126 substance Substances 0.000 abstract description 5
- 239000008107 starch Substances 0.000 abstract description 4
- 230000000694 effects Effects 0.000 abstract description 3
- 239000001254 oxidized starch Substances 0.000 abstract description 2
- 235000013808 oxidized starch Nutrition 0.000 abstract description 2
- 239000001828 Gelatine Substances 0.000 abstract 5
- 229920001744 Polyaldehyde Polymers 0.000 abstract 1
- 239000002671 adjuvant Substances 0.000 abstract 1
- 239000000976 ink Substances 0.000 description 50
- 238000010521 absorption reaction Methods 0.000 description 13
- 239000000049 pigment Substances 0.000 description 8
- 239000007787 solid Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 7
- 239000002245 particle Substances 0.000 description 7
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
- 239000004372 Polyvinyl alcohol Substances 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 229920002451 polyvinyl alcohol Polymers 0.000 description 6
- 229920003169 water-soluble polymer Polymers 0.000 description 6
- 239000004952 Polyamide Substances 0.000 description 5
- 239000003086 colorant Substances 0.000 description 5
- 229920002647 polyamide Polymers 0.000 description 5
- 229920000768 polyamine Polymers 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- 239000003973 paint Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 4
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 230000000740 bleeding effect Effects 0.000 description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 239000001023 inorganic pigment Substances 0.000 description 3
- ZADYMNAVLSWLEQ-UHFFFAOYSA-N magnesium;oxygen(2-);silicon(4+) Chemical compound [O-2].[O-2].[O-2].[Mg+2].[Si+4] ZADYMNAVLSWLEQ-UHFFFAOYSA-N 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- -1 polyethylene Polymers 0.000 description 3
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 3
- 235000012239 silicon dioxide Nutrition 0.000 description 3
- 239000005909 Kieselgur Substances 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- 229910021536 Zeolite Inorganic materials 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 229910052570 clay Inorganic materials 0.000 description 2
- XLIDPNGFCHXNGX-UHFFFAOYSA-N dialuminum;oxygen(2-);silicon(4+) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Al+3].[Al+3].[Si+4] XLIDPNGFCHXNGX-UHFFFAOYSA-N 0.000 description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 239000012860 organic pigment Substances 0.000 description 2
- 239000002985 plastic film Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 239000010457 zeolite Substances 0.000 description 2
- 239000011592 zinc chloride Substances 0.000 description 2
- 235000005074 zinc chloride Nutrition 0.000 description 2
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 241000209761 Avena Species 0.000 description 1
- 235000007319 Avena orientalis Nutrition 0.000 description 1
- 229920002085 Dialdehyde starch Polymers 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229920002873 Polyethylenimine Polymers 0.000 description 1
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000006081 fluorescent whitening agent Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 235000015110 jellies Nutrition 0.000 description 1
- 239000008274 jelly Substances 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000012457 nonaqueous media Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 238000001454 recorded image Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
- B41M5/52—Macromolecular coatings
- B41M5/5236—Macromolecular coatings characterised by the use of natural gums, of proteins, e.g. gelatins, or of macromolecular carbohydrates, e.g. cellulose
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Paper (AREA)
- Duplication Or Marking (AREA)
Abstract
Description
【発明の詳細な説明】
本発明はインクジェット記録シートに関し、インクを以
って画像を形成する為に設げられた受理層のインクの、
吸収能力に優れ、ニジミが少く発色性の優れた多色記録
を与えるインクジェット記録シートに関するものである
。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an inkjet recording sheet, and relates to an ink-receiving layer provided for forming an image using ink.
The present invention relates to an inkjet recording sheet that has excellent absorption capacity, provides multicolor recording with little bleeding and excellent color development.
(従来の技術)
インクジェット記録法は騒音が少(、高速記録および多
色記録がoT能なことから急速に注目されている。しか
し、多色記録を行う場合には。(Prior Art) The inkjet recording method is rapidly attracting attention because of its low noise, high-speed recording, and OT capability of multicolor recording.However, when performing multicolor recording.
2個以上のインクノズルからインクが吐出され記録面上
の一点に2個以上のインク液滴が重なるために、インク
液滴を如何に記録層上で受は止めるかが重要である。イ
ンクは吐出ヘッドの目づまりや、安定性などのために、
染料が水浴性媒体中に非常に薄い濃度で溶解して使用さ
れており1発色にかかわる染料をインク受理層(記録層
)で受は止め、同時に水浴性媒体をすみやかに支持体に
拡散させるか保持もしくは吸収させることが要求される
。通常、支持体上のインク受理層即ちインク吸収に関わ
る膜厚はlOμm前後であるのに対し、ノズルから吐出
されるインク液滴の直径は50〜100μmと5〜10
倍もの大きさである。しかも数ミリ秒以内の微小な時間
で2ヶ以上の液滴を同一面上に受は止め支持体を含む受
理層で保持することが要求される。Since ink is ejected from two or more ink nozzles and two or more ink droplets overlap at one point on the recording surface, it is important how to stop the ink droplets from being received on the recording layer. Due to ink ejection head clogging and stability,
The dye is used dissolved in a water-bathable medium at a very low concentration, and the dye involved in color development is stopped by the ink-receiving layer (recording layer), and at the same time the water-bathable medium is quickly diffused into the support. Retention or absorption is required. Normally, the thickness of the ink receiving layer on the support, that is, the film involved in ink absorption, is around 10 μm, whereas the diameter of the ink droplet ejected from the nozzle is 50 to 100 μm, which is 5 to 10 μm.
It's twice as big. Moreover, it is required to hold two or more droplets on the same surface in a very short period of time, within several milliseconds, with a receiving layer including a support.
従ってインク液が上質紙のようなサイズを添加した紙、
コート紙のような顔料塗工厭又合成紙、プラスチックシ
ートなど拡散吸収の少いか全(その機能含有しない支持
体にインクを滴下又は噴射して多色インクジェット記録
を行うと。Therefore, paper to which the ink liquid has been added has a size similar to that of high-quality paper,
Multicolor inkjet recording is performed by dropping or spraying ink onto a support that has little or no diffusion absorption, such as coated paper, synthetic paper, or plastic sheet.
インク液は記録面上の到達位置から、Z軸方向に拡散、
浸透する前に記録面XY軸方向に拡がり、8Aつだ色の
インク相互の混色による画像の不鮮明さ、画線の乱れ、
画像の品位低下を生ずる。The ink liquid diffuses in the Z-axis direction from the position it reaches on the recording surface.
Before penetrating, it spreads in the XY axis direction of the recording surface, causing blurred images and disordered lines due to color mixing between 8A red inks.
This results in deterioration of image quality.
従って吸収性を有しないか吸収性の少い支持体において
は多色インクジェット記録には全(実用性がないか、単
色に限られた用途が実用性を持つにすぎなかった。Therefore, supports that do not have absorbency or have low absorbency have no practical use in multicolor inkjet recording, or are only practical for use in single colors.
これらの問題を解決するためKm々検討が為されている
。特開昭56−80489号ではインクによって溶解又
は膨潤する物質をインク受理層として設け、インクの保
持を試みている。Many studies have been made to solve these problems. JP-A-56-80489 attempts to retain ink by providing an ink-receiving layer with a substance that dissolves or swells with ink.
又特開昭55−146786号は水溶性高分子として比
較的インク保持能力を付った物質を用いてインクの吸収
能力の増加を図っている。Furthermore, Japanese Patent Application Laid-Open No. 55-146786 attempts to increase the ink absorption capacity by using a water-soluble polymer having a relatively high ink retention capacity.
しかじなh′%らこれらの発明によるインク保持能力を
持つ物¥Jを更に、カラ−1Iiil像密度の高い。In addition, the ink retaining ability according to these inventions has a high color image density.
Ijlち、記録面上の一点に4個以上のインク液滴h″
−重なるような場合又、記録速度を上げた場合Ki2当
然ながらインク吸収能力が不足し、各色がオーバーフロ
ーしてニジミが生じ1画像の鮮明さ、中間調の再現不良
1色のにごすなどのために記録が実用上不適となる。又
、インクセットに長時間を要し本来の高速記録の目的に
達し得ない。特開昭57−173194号は粒子径0、
1〜100μmの吸水性樹脂を結着剤と併用して記録層
を設け、インクジェット記録に用いている。しかしなが
ら吸水性m脂は吸水容量が50−1000倍と非常に大
きい特徴があるものの吸水およびIjl潤時開時間時間
に達する場合があり、インクジェット記録における吸収
時間とは合致しない。加えて非水系媒体には溶解し。4 or more ink droplets at one point on the recording surface
- In case of overlapping, or when the recording speed is increased, Ki2 naturally lacks ink absorption capacity, and each color overflows, causing blurring, resulting in poor clarity of one image, poor reproduction of halftones, and blurring of one color. Records become unsuitable for practical use. Furthermore, it takes a long time to set the ink, making it impossible to achieve the original purpose of high-speed recording. JP-A No. 57-173194 has a particle size of 0,
A recording layer is provided using a water-absorbing resin with a thickness of 1 to 100 μm in combination with a binder, and is used for inkjet recording. However, although water-absorbing m fat has a very large water-absorbing capacity of 50 to 1000 times, the water-absorbing time and Ijl wet-opening time may reach the time, which does not match the absorption time in inkjet recording. In addition, it is soluble in non-aqueous media.
金膜形成が容易な反面、水系媒体中では小粒径に粉砕は
可能であるものの塗膜形成が非常に困ルな欠点を有して
いる。Although it is easy to form a gold film, it has the disadvantage that it is very difficult to form a coating in an aqueous medium, although it can be pulverized to a small particle size.
(発明が解決しようとする問題点)
本発明の目的は纂IKインクの記録層中の吸収能力を増
加し、多色記録の各インクのオーバーフローを防止し、
ニジミのない鮮明な画像を持ち1色再現性の優れたイン
クジェット記録シートを提供することである。(Problems to be Solved by the Invention) The purpose of the present invention is to increase the absorption capacity of IK ink in the recording layer, prevent overflow of each ink in multicolor recording,
To provide an inkjet recording sheet having a clear image without bleeding and excellent one-color reproducibility.
第2にインクの保持機能が高く、インクセットの良い、
高速度インクジェット記録に適した記録シートを提供す
ることである。Secondly, it has a high ink retention function and a good ink set.
An object of the present invention is to provide a recording sheet suitable for high-speed inkjet recording.
(問題点を解決するための手段)
本発明者はインク液滴を受けとめ保持し、且つ、吸収す
る機能の大きな物質を見出し、これをインクジェット記
録シートのインク受理層中に含有させて多色記録の各イ
ンクのオーツ(−フローt−防止し、ニジミのない鮮明
な画像をもち。(Means for Solving the Problem) The present inventor discovered a substance with a large function of receiving, retaining, and absorbing ink droplets, and incorporated it into the ink receiving layer of an inkjet recording sheet to perform multicolor recording. Each ink's oats (-flow t-prevents) and provides clear images without smearing.
且、高速記録性をも合せ持ったインクジェット記録シー
トを得ることに成功した。Furthermore, we succeeded in obtaining an inkjet recording sheet that also has high-speed recording properties.
即ち本発明によれば支持体の上にインク受理J蕾を設け
たインクジェット記録シートにおいて。That is, according to the present invention, in an inkjet recording sheet in which ink-receiving J buds are provided on a support.
水に対する膨調度が30〜60倍である高い膨潤能を有
するゼラチンをインク受理層中に含有させたことを特章
とするインクジェット記録シートが提供されろe
本発明に甲いる高い膨潤能を有するゼラチン(以下高膨
潤性ゼラチンという)はたとえば第1表に示す特性のも
のである。インクジェット記録シートに用いてインクの
吸収能とインクのセットタイム即ち高速性を満し、多色
記録に適4も
に合致し、記録画像の耐光性、耐水性等の特性をも満足
するものである。Provided is an inkjet recording sheet characterized by containing gelatin, which has a high swelling ability that is 30 to 60 times more swellable than water, in an ink-receiving layer. Gelatin (hereinafter referred to as highly swellable gelatin) has, for example, the properties shown in Table 1. It is suitable for use in inkjet recording sheets and satisfies ink absorption capacity and ink set time (high speed), is suitable for multicolor recording, and also satisfies characteristics such as light resistance and water resistance of recorded images. be.
本発明のインクジェット記録シートに設けられるインク
受理層には高膨潤ゼラチンを単独で用いても十分その効
果が得られるが、一方他の水溶性高分子例えばデンプン
、酸化デンプン、リン酸デンプン、カチオン性デンプン
等の各種デンプンおよびその誘導体、変性物、ポリビニ
ルアルコール、カルボキシ変性ポリビニルアルコール、
カチオン変性ポリビニルアルコール、丁セトアセチル化
ポリビニル了ルコール、スチレン−無水マレイン酸共重
金物およびそのアンモニウム変性物、ポリビニルアルコ
ールーアクリル酸エステルーアクリル酸共重合物、ポリ
ビニルアルコール−アクリルアミド−アクリル酸エステ
ル−アクリル酸共重合物およびそのアンモニウム変性物
などを1種又は2種以上併用してもよく、その割合は高
膨潤性ゼラチンlN置部に対し20〜0.05重量部が
望ましい。Although highly swollen gelatin can be used alone in the ink-receiving layer provided in the inkjet recording sheet of the present invention, sufficient effects can be obtained; however, other water-soluble polymers such as starch, oxidized starch, phosphate starch, cationic Various starches such as starch and their derivatives, modified products, polyvinyl alcohol, carboxy-modified polyvinyl alcohol,
Cation-modified polyvinyl alcohol, acetylated polyvinyl alcohol, styrene-maleic anhydride coheavy metal and its ammonium modified product, polyvinyl alcohol-acrylic ester-acrylic acid copolymer, polyvinyl alcohol-acrylamide-acrylic ester-acrylic acid One type or two or more types of copolymers and ammonium-modified products thereof may be used in combination, and the proportion thereof is preferably 20 to 0.05 parts by weight based on the portion of highly swellable gelatin 1N.
更にインク受理I―の耐水性を要求する場合にはホルマ
リン、多価アルデヒド、ジアルデヒドデンプン、ポリエ
チレンイミン、ポリアミドポリアミン、ポリアミドポリ
アミンエポキシ樹脂。Furthermore, when water resistance of ink acceptance I- is required, formalin, polyvalent aldehyde, dialdehyde starch, polyethyleneimine, polyamide polyamine, polyamide polyamine epoxy resin.
などの硬化助剤等の1種又は2種以上を併用することが
望ましい。その割合は高膨潤ゼラチン及び水溶性高分子
の総量に対し50〜5ffiffi’憾が好ましい。こ
の場合インク受理層のベメッキの改善、耐指紋性の向上
等の付与も可能である。It is desirable to use one type or two or more types of curing aids such as the following. The ratio is preferably 50 to 5 ffiffiffi' based on the total amount of highly swollen gelatin and water-soluble polymer. In this case, it is also possible to improve the plating of the ink-receiving layer, improve fingerprint resistance, etc.
本発明のインクジェット記録シートのインク受理層には
1本発明の高膨潤性ゼラチンおよび水溶性高分子に加え
て無機顔料を充填剤として使用することはインクの吸収
性、白色度の向上。In addition to the highly swellable gelatin and water-soluble polymer of the present invention, an inorganic pigment is used as a filler in the ink-receiving layer of the inkjet recording sheet of the present invention, which improves ink absorption and whiteness.
コントラストの向上に有効であり、更に顔料の粒子径を
コントロールすることによりドツト径のコントロールが
可能である。この目的に使用可能な顔料としては例えば
炭酸カルシウム、クレー、ゼオライト、タルク、硫酸バ
リウム、LVi化亜鉛亜鉛タンホワイト、酸化チタン、
合成ケイ酸アルミニウム、合成ケイ酸アルミニウム・マ
グネシウム、合成ケイ酸マグネシウム、水酸化アルミニ
ウム、合成ケイ酸、珪藻土、水酸化マグネシウム、ポリ
スチレン又はポリエチレン微粉末、尿素樹脂微粉末など
の無機、有機顔料がある。これらは高膨潤セラチンおよ
び水溶性高分子1重量部に対し、0〜10重f部が過当
である。It is effective in improving contrast, and furthermore, by controlling the particle size of the pigment, the dot size can be controlled. Pigments that can be used for this purpose include, for example, calcium carbonate, clay, zeolite, talc, barium sulfate, zinc chloride LVi, titanium oxide,
There are inorganic and organic pigments such as synthetic aluminum silicate, synthetic aluminum/magnesium silicate, synthetic magnesium silicate, aluminum hydroxide, synthetic silicic acid, diatomaceous earth, magnesium hydroxide, polystyrene or polyethylene fine powder, and urea resin fine powder. The appropriate amount of these is 0 to 10 parts by weight per 1 part by weight of highly swollen seratin and water-soluble polymer.
インク受理層を形成する他の添加剤としては。Other additives that form the ink receiving layer include:
インク染料の定着剤、インクの耐光性を向上させる紫外
線吸収剤、父、顔料の分散剤、顔料の凝結助剤、消泡剤
、防腐剤、螢光増白剤、粘度安定剤などがあり、これら
は目的に応じて使用できる、
支持体としては紙、合成舐、プラスチックフィルムなど
が使用できる。These include fixing agents for ink dyes, ultraviolet absorbers that improve the light resistance of ink, pigment dispersants, pigment setting aids, antifoaming agents, preservatives, fluorescent whitening agents, viscosity stabilizers, etc. These can be used depending on the purpose. Paper, synthetic film, plastic film, etc. can be used as the support.
高膨潤性ゼラチンを含むインク受理層の下塗層を設ける
ことはインクの吸収ムラを改良するた2めに有効であり
、他忙、濃度、コントラスト。Providing an ink-receiving subbing layer containing highly swellable gelatin is effective for improving uneven absorption of ink, improving density, density, and contrast.
インクの吸収性も改善できる。Ink absorption can also be improved.
これらの目的のために0.2〜15μの粒子径をもった
無機顔料、有機顔料、プラスチックピグメント、例えば
炭酸カルシウム、クレー、ゼオライト、タルク、硫酸バ
リウム、1*化亜鉛。For these purposes, inorganic pigments, organic pigments, plastic pigments with a particle size of 0.2 to 15 μm, such as calcium carbonate, clay, zeolite, talc, barium sulfate, zinc chloride.
チタンホワイト、合成ケイ酸アルミニウム、合成ケイ酸
マグネシウム、合成ケイ酸アルミニウム・マグネシウム
、合成ケイ酸、珪藻土、ポリエチレン微粉末、ポリスチ
レン微粉末、尿素樹脂微粉末などを1noii部に対し
結着剤5〜20恵曾部混合した塗被物を使用できる。結
着剤としては本発明の晶膨潤ゼラチンおよび前述の水溶
性高分子を使用してもさしつかえない。Titanium white, synthetic aluminum silicate, synthetic magnesium silicate, synthetic aluminum/magnesium silicate, synthetic silicic acid, diatomaceous earth, polyethylene fine powder, polystyrene fine powder, urea resin fine powder, etc. per 1 noii part of binder 5 to 20 Esobe mixed coating materials can be used. As the binder, the crystal-swollen gelatin of the present invention and the water-soluble polymer described above may be used.
下塗層の塗工量は2〜20 f/l?が適当であり。Is the coating amount of the undercoat layer 2-20 f/l? is appropriate.
顔料の粒子稗、顔料と結着剤の割合を変えてインク受理
層とのバランスをとることが望ましい。It is desirable to balance the pigment with the ink-receiving layer by changing the particle size of the pigment and the ratio of the pigment to the binder.
本発明のインク受理I@は片面当り塗工量0.5〜20
9々、好ましい範囲は2〜1597%である。支持体の
片佃への塗工に限らず必要により両側への塗工も可能で
ある。The ink acceptance I@ of the present invention is 0.5 to 20 coated per side.
9, the preferred range is 2 to 1597%. Coating is not limited to only one side of the support, but can also be applied to both sides if necessary.
塗工には一般に使用されている塗工方法、塗工装置ab
−使用できる。例えばエアナイフコーター、ブレードコ
ーター、グラピアコーター、カーテンコーター、バーコ
ーター、ロールコータ−、サイズプレスコーター、ケー
トロールコータ−などが使用できる。塗工後、必要に応
じてカレンダー処理を行って塗工面を平滑にすることが
望ましい。Generally used coating methods and coating equipment ab
-Can be used. For example, an air knife coater, a blade coater, a graphia coater, a curtain coater, a bar coater, a roll coater, a size press coater, a Kate roll coater, etc. can be used. After coating, it is desirable to perform calender treatment as necessary to smooth the coated surface.
又耐水性を発現するために適当な温度で熱処理を行って
もよい。なおゼラチンは30℃以下ではゼリー状になる
ため適度な温度管理が必要である。Further, heat treatment may be performed at an appropriate temperature in order to develop water resistance. Note that gelatin becomes jelly-like at temperatures below 30°C, so appropriate temperature control is required.
本発明におけるvF性値および特性の測定は以下の条件
で行った。Measurement of vF properties and characteristics in the present invention was carried out under the following conditions.
インク吸収性
IBM3852カラーインクジェットプリンタ−で混色
2複打ちを行い、この時各インクのニジミがな(1秒後
完全にインク受理層に吸収されている場合を○とする。Ink-absorbing IBM 3852 color inkjet printer was used to print two mixed colors, and at this time, each ink did not bleed (a case where the ink was completely absorbed into the ink-receiving layer after 1 second is marked as ○).
実施例1〜3および比較例1〜2に適用する。This applies to Examples 1-3 and Comparative Examples 1-2.
インクセットタイム
実施例4比較例3に適用する。比較f!AI 3に61
11定方法を記述した。Ink set time Example 4 Applied to Comparative Example 3. Comparison f! AI 3 to 61
11 specific methods have been described.
耐水性
記録シートを流水に浸漬し、5分後インク受Fl!層が
剥離ないし浴は出している場合を×とする。Immerse the water-resistant recording sheet in running water, and after 5 minutes, ink receiver Fl! If the layer has peeled off or the bath has come out, it is marked as ×.
耐光性
IBM3852カラーインクジェットプリンターでペタ
印字を行い、フェードメーターに24時間曝露し、黒色
の残存率50憾以下を×とする。A light-fast IBM 3852 color inkjet printer is used to perform peta printing, and exposure to a fade meter is performed for 24 hours, and a black residual rate of 50 or less is marked as x.
ドツト径
キャノンA1210インクジエツトプリンターで印字し
、100倍ルーペで黒色部分のドツト径を測定する。Dot diameter Print with a Canon A1210 inkjet printer, and measure the dot diameter of the black part with a 100x loupe.
ニジミ
IBM3852カラーインクジェットプリンターで2度
重ね打のペタ印字を行い、この時混色部のインクの流れ
出しを観察し、後からインク受理NK当ったインク液7
8が流れ出している場合を×とする。Nijimi IBM 3852 color inkjet printer performs double-print peta printing, observing the flow of ink in the color mixing area, and later checking the ink liquid 7 that has hit the ink receiving NK.
The case where 8 is flowing out is marked as ×.
(実tM例)
実施例1
市販の上質紙64t/−に平均粒子径7μmの合成ケイ
酸アルミニウム100 Hrls、カルボキシ変性ポリ
ビニルアルコールの104[1100部、ゼラチンD)
の104溶液100部および20係ポリアミドポリアミ
ン工ポキシ樹T4¥130部。(Actual tM example) Example 1 100 Hrls of synthetic aluminum silicate with an average particle size of 7 μm, 104 [1100 parts of carboxy-modified polyvinyl alcohol, gelatin D] on 64 tons/- of commercially available high-quality paper.
100 parts of 104 solution and 130 yen parts of polyamide polyamine engineered poxy tree T4 of 20 series.
よりなる固形分25憾の塗料を固形分で片面152/f
?となるようにメイヤーバーで塗工、乾燥し。Paint with a solid content of 25 ml on one side with a solid content of 152/f
? Coat with a Meyer bar and dry.
前記の方法で特性を評価し第2表の結果を得た。The properties were evaluated using the method described above, and the results shown in Table 2 were obtained.
実施例2
市販合成紙ユボ60μの上に合成シリカ(水沢化学工業
株式会社製p−78)10(1部、ポリビニルアルコー
ル−メチルメタクリレート−アクリル酸共重合物の20
係液100部、ゼラチンの)の154尋液300部およ
び20憾ポリアミドポリアミン工ポキシftttli&
loo部よりなる固形分20媛の塗料を固形分で片面1
0 f/rrlメイヤーバーで塗工、乾燥し、特性の評
価を行い第2表の結果を得た。Example 2 Synthetic silica (p-78 manufactured by Mizusawa Chemical Industry Co., Ltd.) 10 parts (1 part, 20 parts of polyvinyl alcohol-methyl methacrylate-acrylic acid copolymer) was placed on commercially available synthetic paper 60 μm.
100 parts of gelatin solution, 300 parts of 154 fat solution of gelatin and 20 parts of polyamide polyamine engineered poxy ftttli &
One side of the paint with a solid content of 20 yen consisting of the loo part
It was coated with a 0 f/rrl Mayer bar, dried, and evaluated for characteristics, and the results shown in Table 2 were obtained.
実施例3
市販上質紙642汐の上にまず合成シリカ(水沢化学工
業株式会社製ジルトンLP105 ) 100部と炭酸
カルシウム(白石カルシウム株式会社製PC)50M、
ポリビニルアルコール10%溶液200部よりなる固形
分204の塗料を固形分で片面5f//メイヤーパーで
塗工、乾燥して下塗層を形成した後、この上に平均粒子
径5μmの合成ケイ酸アルミニウムIC)0部、ポリビ
ニルアルコール−アクリルアミド−アクリル酸エステル
−アクリル酸共重合物の104i液100部、ゼラチン
(C115’1醐液100部および20係ポリアミドポ
リアミン工ポキシIN脂40部よりなる固形分28憾の
塗料を固形分で片面1゜t/rrlメイヤーバーで塗工
、乾燥し特性の評価を行い第2表の結果を得た。Example 3 First, 100 parts of synthetic silica (Jilton LP105 manufactured by Mizusawa Chemical Co., Ltd.) and 50 M of calcium carbonate (PC manufactured by Shiraishi Calcium Co., Ltd.) were placed on commercially available high-quality paper 642 paper.
A paint with a solid content of 204 made of 200 parts of a 10% solution of polyvinyl alcohol was coated with a solid content of 5 f///mayer par on one side, dried to form an undercoat layer, and then synthetic silicic acid with an average particle size of 5 μm was applied on top of this. Solid content consisting of 0 parts of aluminum IC), 100 parts of 104i liquid of polyvinyl alcohol-acrylamide-acrylic acid ester-acrylic acid copolymer, gelatin (100 parts of C115'1 liquid and 40 parts of 20% polyamide polyamine engineered poxy IN resin) 28 pieces of paint was applied with a solid content of 1°t/rrl on one side using a Mayer bar, dried, and the properties were evaluated, and the results shown in Table 2 were obtained.
実施例4
ゼラチン■)の1596水済液を、市販ポリエステルフ
ィルム(商品名 三菱ダイヤフォイル100μmコロナ
処理品)の上に固形分で8f/d塗布、乾燥し、インク
ジェット記録用透明シートを得た。その結果を第2表に
示す。Example 4 A 1596 watered liquid of gelatin (1) was coated on a commercially available polyester film (trade name: Mitsubishi Diafoil 100 μm corona treated product) at a solid content of 8 f/d and dried to obtain a transparent sheet for inkjet recording. The results are shown in Table 2.
比較例1
ゼラチン0に代えて市販ゼラチン(5)を使った以外は
実施例1と同様にして第2表の結果を得た。Comparative Example 1 The results shown in Table 2 were obtained in the same manner as in Example 1, except that commercially available gelatin (5) was used in place of gelatin 0.
比較例2
ゼラチン(DJに代えてゼラチンC)を使った以外は実
施例1と同様にして第2表の結果を得た。Comparative Example 2 The results shown in Table 2 were obtained in the same manner as in Example 1, except that gelatin (gelatin C instead of DJ) was used.
比較例3
ゼラチン(4)を甲いた他は実施例4と同様にしてイン
クジェット記録用透明シートを得た。Comparative Example 3 A transparent sheet for inkjet recording was obtained in the same manner as in Example 4, except that gelatin (4) was added.
実施例4と比較例3の記録シートにキャノンA1210
カラーインクジエツトプリンターを用い、シアン、イエ
ロー、マゼンタ、ブラックの単色およびシアンとイエロ
ー、シアンとマゼンタ、イエローとマゼンタの混色計7
色をフルドツトで記録後、濾紙を記録面に当て、0.5
kV′cdの圧力を2秒かけて濾紙にインク跡が付着
しな(なるまでの時間を測定し、インクセットタイムと
した。その結果を第2表に示す。Canon A1210 on the recording sheets of Example 4 and Comparative Example 3
Using a color inkjet printer, a total of 7 colors can be printed, including single colors of cyan, yellow, magenta, and black, and mixed colors of cyan and yellow, cyan and magenta, and yellow and magenta.
After recording the color in full dots, place a filter paper on the recording surface and
A pressure of kV'cd was applied for 2 seconds, and the time until no ink marks were left on the filter paper was measured, which was defined as the ink setting time. The results are shown in Table 2.
第1表 ゼラチン特性 注1) 20℃の蒸留水を満たした容器中に。Table 1 Gelatin properties Note 1) In a container filled with distilled water at 20℃.
325メツシユの金網でっ(られた上部のみh’ iF
I口した円筒容器を頭部を水面に突出させた状態で沈め
、該円笥容2非の上部開口部より、50メツシユの分析
篩をパスした粉末状ゼラチン1fを投入し、投入後10
秒で円筒容器を引上げ、投入した12のゼラチンが吸収
した水の上滑を測定してh・ン潤度とする、
注2) BIαh式ゼリー強度計により測定。Only the upper part is covered with wire mesh of 325 mesh.
Submerge a cylindrical container with its head protruding above the water surface, and pour 1f of powdered gelatin that has passed a 50-mesh analytical sieve through the upper opening of the cylindrical container.
The cylindrical container is pulled up in seconds, and the amount of water absorbed by the 12 gelatin added is measured to determine the moisture content. Note 2) Measured using a BIαh type jelly strength meter.
注3) B100m式粘度計によりd(11定。Note 3) d (11 constant) determined by B100m viscometer.
第2表
(発明の効果)
第2表に示した結果で明らかなように1本発明による実
施例1〜4で得られた記録シートでは、インクの吸収性
、インクのニジミ、インクセットタイムとも優れている
が、従来技術による比較甲シートでは各特性を満足する
ことはできない。Table 2 (Effects of the Invention) As is clear from the results shown in Table 2, the recording sheets obtained in Examples 1 to 4 according to the present invention had poor ink absorption, ink bleeding, and ink set time. Although it is excellent, the comparative sheet made by the prior art cannot satisfy each characteristic.
Claims (1)
録シートにおいて、該インク受理層に、水に対する膨潤
度が30〜60倍であるゼラチンを含有したことを特徴
とするインクジェット記録シート。An inkjet recording sheet comprising an ink-receiving layer provided on a support, the ink-receiving layer containing gelatin having a swelling degree of 30 to 60 times with respect to water.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6075186A JPS62218180A (en) | 1986-03-20 | 1986-03-20 | Ink jet recording sheet |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6075186A JPS62218180A (en) | 1986-03-20 | 1986-03-20 | Ink jet recording sheet |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS62218180A true JPS62218180A (en) | 1987-09-25 |
Family
ID=13151287
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6075186A Pending JPS62218180A (en) | 1986-03-20 | 1986-03-20 | Ink jet recording sheet |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62218180A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6375200A (en) * | 1986-09-17 | 1988-04-05 | 山陽国策パルプ株式会社 | Writing sheet and erasure of writing part on said sheet |
JPH01190483A (en) * | 1988-01-27 | 1989-07-31 | Canon Inc | Material to be recorded |
EP0363989A2 (en) * | 1988-10-14 | 1990-04-18 | Fuji Photo Film Co., Ltd. | Thermal transfer image receiving materials |
JPH03136891A (en) * | 1989-07-06 | 1991-06-11 | E I Du Pont De Nemours & Co | Improvement element as non-impact printing receptor |
EP0445327A1 (en) * | 1990-03-07 | 1991-09-11 | Felix Schoeller jr. Papierfabrik GmbH & Co. KG | Recording medium for ink-jet printing |
EP0933411A1 (en) * | 1996-08-21 | 1999-08-04 | Idemitsu Petrochemical Co., Ltd. | Coating materials for forming information display surfaces and display medium |
WO2004054813A1 (en) * | 2002-12-13 | 2004-07-01 | Fuji Photo Film B.V. | Ink-jet recording medium |
-
1986
- 1986-03-20 JP JP6075186A patent/JPS62218180A/en active Pending
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6375200A (en) * | 1986-09-17 | 1988-04-05 | 山陽国策パルプ株式会社 | Writing sheet and erasure of writing part on said sheet |
JPH01190483A (en) * | 1988-01-27 | 1989-07-31 | Canon Inc | Material to be recorded |
EP0363989A2 (en) * | 1988-10-14 | 1990-04-18 | Fuji Photo Film Co., Ltd. | Thermal transfer image receiving materials |
JPH03136891A (en) * | 1989-07-06 | 1991-06-11 | E I Du Pont De Nemours & Co | Improvement element as non-impact printing receptor |
EP0445327A1 (en) * | 1990-03-07 | 1991-09-11 | Felix Schoeller jr. Papierfabrik GmbH & Co. KG | Recording medium for ink-jet printing |
JPH04216990A (en) * | 1990-03-07 | 1992-08-07 | Felix Schoeller Jr Gmbh & Co Kg | Recording material having glossy face for ink jet printing |
EP0933411A1 (en) * | 1996-08-21 | 1999-08-04 | Idemitsu Petrochemical Co., Ltd. | Coating materials for forming information display surfaces and display medium |
EP0933411A4 (en) * | 1996-08-21 | 2000-10-04 | Idemitsu Petrochemical Co | Coating materials for forming information display surfaces and display medium |
WO2004054813A1 (en) * | 2002-12-13 | 2004-07-01 | Fuji Photo Film B.V. | Ink-jet recording medium |
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