JPH0216705B2 - - Google Patents
Info
- Publication number
- JPH0216705B2 JPH0216705B2 JP13467983A JP13467983A JPH0216705B2 JP H0216705 B2 JPH0216705 B2 JP H0216705B2 JP 13467983 A JP13467983 A JP 13467983A JP 13467983 A JP13467983 A JP 13467983A JP H0216705 B2 JPH0216705 B2 JP H0216705B2
- Authority
- JP
- Japan
- Prior art keywords
- ink
- inorganic powder
- elastic material
- impregnated body
- organic elastic
- 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.)
- Expired
Links
- 239000000843 powder Substances 0.000 claims description 52
- 239000002245 particle Substances 0.000 claims description 29
- 239000013013 elastic material Substances 0.000 claims description 28
- 239000000463 material Substances 0.000 claims description 22
- 239000007788 liquid Substances 0.000 claims description 17
- 239000010419 fine particle Substances 0.000 claims description 15
- 239000000835 fiber Substances 0.000 claims description 11
- 229920001971 elastomer Polymers 0.000 claims description 7
- 239000005060 rubber Substances 0.000 claims description 7
- 229920005989 resin Polymers 0.000 claims description 6
- 239000011347 resin Substances 0.000 claims description 6
- 229920005992 thermoplastic resin Polymers 0.000 claims description 6
- 229920001187 thermosetting polymer Polymers 0.000 claims description 6
- 229920002725 thermoplastic elastomer Polymers 0.000 claims description 5
- GBAOBIBJACZTNA-UHFFFAOYSA-L calcium sulfite Chemical compound [Ca+2].[O-]S([O-])=O GBAOBIBJACZTNA-UHFFFAOYSA-L 0.000 description 9
- 235000010261 calcium sulphite Nutrition 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 239000007822 coupling agent Substances 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 238000005245 sintering Methods 0.000 description 6
- 238000005299 abrasion Methods 0.000 description 5
- 239000004814 polyurethane Substances 0.000 description 5
- 239000011148 porous material Substances 0.000 description 5
- 229920000459 Nitrile rubber Polymers 0.000 description 4
- -1 polyethylene Polymers 0.000 description 4
- 229920002635 polyurethane Polymers 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- 239000003822 epoxy resin Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 239000010445 mica Substances 0.000 description 2
- 229910052618 mica group Inorganic materials 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000005498 polishing Methods 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 239000010456 wollastonite Substances 0.000 description 2
- 229910052882 wollastonite Inorganic materials 0.000 description 2
- IEKHISJGRIEHRE-UHFFFAOYSA-N 16-methylheptadecanoic acid;propan-2-ol;titanium Chemical compound [Ti].CC(C)O.CC(C)CCCCCCCCCCCCCCC(O)=O.CC(C)CCCCCCCCCCCCCCC(O)=O.CC(C)CCCCCCCCCCCCCCC(O)=O IEKHISJGRIEHRE-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 239000004970 Chain extender Substances 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229920000271 Kevlar® Polymers 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- 229920006311 Urethane elastomer 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
- 239000002253 acid Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 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
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- HTDKEJXHILZNPP-UHFFFAOYSA-N dioctyl hydrogen phosphate Chemical compound CCCCCCCCOP(O)(=O)OCCCCCCCC HTDKEJXHILZNPP-UHFFFAOYSA-N 0.000 description 1
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000004761 kevlar Substances 0.000 description 1
- 230000005389 magnetism Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920003225 polyurethane elastomer Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 238000003856 thermoforming Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229920006305 unsaturated polyester Polymers 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41J—TYPEWRITERS; SELECTIVE PRINTING MECHANISMS, i.e. MECHANISMS PRINTING OTHERWISE THAN FROM A FORME; CORRECTION OF TYPOGRAPHICAL ERRORS
- B41J27/00—Inking apparatus
- B41J27/10—Inking apparatus with ink applied by rollers; Ink supply arrangements therefor
Landscapes
- Impression-Transfer Materials And Handling Thereof (AREA)
Description
本発明はインク含浸体に関する。さらに詳しく
は、本発明は強靭で耐摩耗性および寸法安定性に
すぐれ、かつ良好な弾性と空〓率を有するインク
ロール、インクパツドなどのインク含浸体に関す
る。
従来より、インクロール、インクパツドなどの
インク含浸体としては、アクリロニトリル−ブタ
ジエンゴム、ポリウレタン、ナイロンなどのポリ
マー粉末をモールド内に充填し、高温で加熱焼結
して微細孔を有する多孔質体を成形し、ついで該
多孔質体にインクを含浸させる、いわゆる焼結法
より製造されたのがよく知られている。
しかしながら、前述のごときポリマー粉末を単
に焼結により一体化するばあいにおいては、焼結
に多量の熱量を必要とし、かつ所望の空〓率をう
ることが困難であり、所望のインク含浸率でかつ
すぐれたインク滲出性を有する強靭で適度な弾性
を有する多孔質体を製造しえないという欠点があ
る。
また、無機または有機の微粒末粒子の表面全体
に熱可塑性エラストマーの被膜を形成したものを
焼結して多孔質体をえ、これにインクを含浸させ
たものも知られている(特開昭53−23357号公報
参照)。しかし、このものにおいても前記のもの
と同様な欠点があり、以前として空〓率の低いも
のであつた。
本発明は叙上の欠点を排除すべく完成されたも
のであつて、その要旨とするところは、外周面に
有機弾性材の微粒子が相互に間隔を配して多数付
着されてなる無機粉末粒子が骨格材とされ、前記
有機弾性材の微粒子によつて、前記骨格材が相互
に固着されてなる連続多孔質体にインクが含浸さ
れてなるインク含浸体にある。
本発明のインク含浸体は、無機粉末粒子が有機
弾性材微粒子によつて相互に固着された構造よ
り、従来のものにくらべ強靭性、耐摩耗性および
空〓率のいずれにおいてもすぐれ、インクをイン
クリボンあるいは活字などに補給するのに良好な
耐久性を有する。
本発明に用いる無機粉末としては、たとえばカ
ーボンブラツク、炭酸カルシウム、亜硫酸カルシ
ウムなどの圧縮特性にすぐれた軟質無機粉末やシ
リカ、ケイ酸アルミニウム、クレーなどの引張強
さにすぐれた硬質無機粉末、さらにチタン酸カリ
ウム、ワラストナイト、タルク、マイカなどの引
張強さおよび圧縮特性を高めるものがあげられ
る。
本発明における有機弾性材微粒子用の材料とし
ては、たとえば熱可塑性樹脂や熱可塑性ゴム、熱
硬化性樹脂または反応性液状ゴムがあげられる。
前記熱可塑性樹脂としては、たとえばポリ塩化
ビニル、ポリエチレン、ポリプロピレン、ポリエ
チレンテレフタレート、ポリブチレンテレフタレ
ート、ポリアミド、ポリアミド共重合体などがあ
げられる。また熱可塑性ゴムとしては、たとえば
ポリウレタン、アクリロニトリル−ブタジエンゴ
ムなどがあげられる。これら熱可塑性樹脂、熱可
塑性ゴムは溶融状態で付着される。
また熱硬化性樹脂としては、たとえばポリウレ
タン、エポキシ樹脂、不飽和ポリエステル、ジア
リルフタレート樹脂などがあげられ、さらに反応
性液状ゴムとしては、たとえば液状ウレタンゴ
ム、液状ブタジエン−スチレンゴム、液状アクリ
ロニトリル−ブタジエンゴム、液状クロロプレン
ゴムなどがあげられる。これらの熱硬化性樹脂お
よび反応性液状ゴムはいずれも液状であるか、あ
るいは比較的低い温度で液状化するものである。
つぎに前記無機粉末粒子の外表面に有機弾性材
微粒子を付着して骨格材を製造する方法およびえ
られた骨格材の成形法について説明する。
有機弾性材は液状で無機粉末粒子の表面上にい
くらかの間〓をもつて付着するように無機粉末と
混合され、無機粉末粒子の外表面に有機弾性材微
粒子が相互に間隔をもつて多数付着した構造の骨
格材をうる。第1図はこのようにしてえられた骨
格材の一例を示す概略断面図であつて、無機粉末
粒子1に対して有機弾性材微粒子2が粒子相互の
間の間〓をもつて多数付着せられていることによ
り、えられる多孔質体の空〓率をきわめて大なら
しめることができ、さらに有機弾性材の混合量を
適宜変えることにより所望の空隙率を有する多孔
質体がえられるというすぐれた利点が発揮され
る。かかる無機粉末粒子1は粒径が5〜150μで
あつて、かつ球状あるいはそれに近いもの(たと
えば楕円体など)が好ましい。
このようにして有機弾性材微粒子2が無機粉末
粒子1に付着された骨格材はモールド内に振動子
を利用する無圧充填法により均一に充填され、熱
風による加熱処理によつて焼結した多孔質体がえ
られる。かくして本発明においては、その焼結に
要する熱量をきわめてすくなくすることができる
という利点がある。
有機弾性材は無機粉末粒子の表面に粒子相互の
間に間〓をもつて付着されており、かかる骨格材
を加熱成形によつて互いに接合せしめ、かつ弾性
を付着させるものである。
有機弾性材は無機粉末とあらかじめ液体の状態
で混合したのち、モールド内に充填されるか、あ
るいはモールド内に各材料を投入し、混合して使
用するなどの方法があげられる。有機弾性材とし
て熱可塑性樹脂を用いるばあい、該熱可塑性樹脂
は加熱溶融した状態で無機粉末と混合され、モー
ルド内で冷却固化される。また液状の熱硬化性樹
脂はモールド内での加熱成形によつて重縮合し、
硬化せられ、さらに反応性液状ゴムは同様にモー
ルド内での加熱処理によつて架橋し、硬化せられ
る。
有機弾性材の配合量は用いる材料の種類によつ
て適宜変更されるものであるが、無機粉末と有機
弾性材の総量に対して10〜50%(重量%、以下同
様)、なかんづく20〜35%であるのが好ましい。
なお無機粉末と有機弾性材との接着性を向上さ
せるうえで、イソプロピルトリ(ジオクチルホス
フエート)チタネート、イソプロピルトリイソス
テアロイルチタネートなどのチタネート系カツプ
リング剤、さらにシラン系カツプリング剤、ジル
コネート系カツプリング剤、アルミニウム系カツ
プリング剤、カルシウム系カツプリング剤などの
カツプリング剤を用いるのが好ましい。かかるカ
ツプリング剤は無機粉末の表面接着性を改善し、
強固な接着強度を付与せしめ、さらに液状の有機
弾性材に対して粘度調整剤として作用すると共
に、硬化触媒としての機能をも有する。
本発明における無機粉末の形状としては球状、
繊維状、板状(フレーク状)などの種々の形状が
いずれも好適に採用される。
たとえば無機粉末がほぼ球状であるばあい、前
述のごとき振動子による無圧充填法(たとえば平
行菱形充填法など)によつて、モールド内での粉
末粒子は第2図で示されるように配列されるが、
本発明においては第1図で示されるように有機弾
性材微粒子2が表面上に適宜な間〓をもつて付着
されているので第3図で示されるごとき配列とな
り、その空〓率をきわめて大きくすることができ
る。ちなみに第2図で示されるごとき配列におい
て空隙率が約25容量%であるが、第3図で示され
るものにおいてはその空隙率を60〜75容量%まで
高めることが可能である。
無機粉末が短繊維状(たとえばチタン酸カリウ
ム、ワラストナイトなどの単結晶繊維で、アスペ
クト比が10〜50:1、径が15〜30μ)であるばあ
い、配合すると一軸的に強度を高めることができ
るが、これらを無配向でモールド内に充填するこ
とにより、その空〓を大きくすることができる。
また無機短繊維に有機短繊維(たとえばデユポン
社製のケブラー繊維などの芳香族ポリアミド維、
カーボン繊維、グラフアイト繊維、ポリエステル
繊維など)を混合して用いるのが強靭化を高める
うえで好ましい。
また板状粉末(たとえばカオリン、タルクであ
り、代表的にはマイカがあげられ、該マイカは巾
1.4〜4μで厚さ40μ以下、通常2〜3μであり、その
フレークアスペクト比が4:1〜100:1)であ
るばあいも前記短繊維状のばあいと同様に無配向
あるいは一軸配向的にモールド内に充填すればよ
い。さらにこれらの各形状を有する無機粉末を併
用することにより、空〓率を大きくすることもで
きる。
本発明においては、無機粉末粒子に有機弾性材
微粒子を付着せしめた骨格材をモールド内に充填
したのち、有機弾性材微粒子を速やかに溶融して
焼結させ、冷却して固化させるか、加熱硬化させ
るものであつて、処理時間を短縮させるためにあ
らかじめ遠赤外線照射などにより予備加熱するの
が好ましい。
また加熱成形後、えられる多孔質体を有機弾性
材を溶解するアルコール、アセトン、ベンゼン、
キシレン、ジメチルホルムアミドなどの溶剤と水
などの非溶剤との混合溶液に浸漬させるか、好ま
しくはこれらの溶剤の磁気と接触させるなどして
多孔質体表面の薄膜を除去あるいは収縮させて微
細孔をあけ、均一なポーラス化をはかるのが好ま
しい。
かくしてえられる多孔質体へのインクの含浸は
通常のインクパツドおよびインクロールにおいて
採用されるインク含浸法が好適に採用されうる。
以上述べたごとく、本発明は種々の形状をとり
うる無機粉末粒子の外表面に有機弾性材の微粒子
が粒子相互の間に間隙をもつて付着された構造の
骨格材を、無機粉末などを用いる通常の焼結条件
に比してはるかに低い温度条件下での短時間の加
熱加圧成形によつて強固に接合したものであつ
て、無機粉末の有する強靭さ、耐摩耗性、寸法安
定性などのすぐれた性質を具備し、かつインクロ
ールまたはインクパツドとして好適な大きさの空
〓を有する多孔質体を簡単に製造することができ
るというすぐれた利点を有する。
つぎに実施例をあげて本発明を説明する。
実施例 1
平均粒径5μの球状亜硫酸カルシウム粉末を高
せん断撹拌機中で撹拌しながら、溶融したナイロ
ン66を総量に対して20%の割合で霧状に噴霧して
該亜硫酸カルシウム粉末粒子の外表面に液滴相互
の間に間〓をもつて付着させ、ついで冷却した。
えられた付着亜硫酸カルシウム粉末をリボンブ
レンダーで打撃、振動を与え、凝集した粉末を充
分にときほぐしたのち、所定量を直径20mmφ、長
さ40mmの空〓をもつモールド内に充填し、加圧下
で200℃で5分間加熱成形し、ついで放冷して多
孔質体をえた。このものに油性インクを含浸させ
てインク含浸体をえた。
実施例 2
平均粒径10μの球状亜硫酸カルシウム粉末を高
せん断撹拌機中で撹拌しながら、液状ポリウレタ
ン〔常温硬化性ポリウレタン樹脂ADAPT60L
(国際ケミカル(株)製)10重量部に硬化剤(液状イ
ソシアネート)3重量部を配合した液状ポリウレ
タン〕を総量に対して15%の割合で糸状に注下
し、亜硫酸カルシウム粉末粒子の外表面に液滴相
互の間に間〓をもつて付着させた。
えられた付着亜硫酸カルシウム粉末をリボンブ
レンダーで打撃、振動を与え、凝集した粉末を充
分にときほぐしたのち、所定量を直径25mmφ、長
さ50mmの空〓をもつモールド内に充填し、100℃
で5分間加熱成形して多孔質体をえた。このもの
に油性インクを含浸させてインク含浸体をえた。
実施例 3
平均粒径12μの球状亜硫酸カルシウム粉末を高
せん断撹拌機中で撹拌しながら、反応性液状ゴム
組成物〔ハイカーCTBN 1300 X8(ビー・エフ・
グツドリツチ・ケミカル社製のニトリルゴム)
143重量部、ビスフエノールA(鎖延長剤)24重量
部、エポキシ樹脂RA 10A((国際ケミカル(株)製)
100重量部およびエポキシ樹脂硬化剤RA 10B(国
際ケミカル(株)製)100重量部を配合した組成物〕
を総量に対して10%の割合で定量混合吐出機を用
いて注入し、亜硫酸カルシウム粉末粒子の外表面
に液滴相互の間に間〓をもつて付着させた。
えられた付着亜硫酸カルシウム粉末を実施例1
と同様にしてリボンブレンダーでときほぐし、モ
ールド内に充填して40℃で7.5分ゲル化させ、さ
らに常温で30分間硬化させて多孔質体をえた。こ
のものに油性インクを含浸させてインク含浸体を
えた。
比較例
平均粒径65μのナイロン6粉末を内に充填し、
加圧下で160℃で10分間予備加熱成形したのち、
260℃の熱雰囲下中で3分間焼成してえられた多
孔質体を冷却乾燥し、ついで油性インクを含浸さ
せてインク含浸体をえた。
実施例1〜3および比較例でえた各インク含浸
体の強靭性、耐摩耗性および空隙率を調べた。そ
の結果を第1表に示す。
第1表における各試験項目の試験件は以下のと
おりである。
(1) 強靭性
引張強さおよび伸びはJIS K 6301に記載の
引張試験法に準拠した。
また引張応力は試験片(外径44.6mmφ、内径
36.6mmφ、長さ57.5mm)に50%の伸びを与えた
とき引張荷重を測定して求めた。
(2) 摩耗率
イギリス規格BS 903 part A9C法に準拠し
て摩耗度を測定した。
すなわちアクロン式摩耗試験機にて試料(厚
さ10mm、巾14mm)に、1.4Kg(3ポンド)の荷
重をかけ、該試料と研磨盤の回転面との傾斜角
度を15゜として研磨盤を回転させ、摩耗重量を
測定して摩耗した割合を求めた。
(3) 空〓率
空〓率は次式により求めた。
(1−W/d×V)×100
W:インクを含まない多孔質体の重量
V:多孔質体の体積
d:多孔質体構成物質の比重
The present invention relates to an ink-impregnated body. More specifically, the present invention relates to ink-impregnated bodies such as ink rolls and ink pads that are tough, have excellent abrasion resistance and dimensional stability, and have good elasticity and porosity. Traditionally, ink-impregnated bodies such as ink rolls and ink pads have been made by filling polymer powders such as acrylonitrile-butadiene rubber, polyurethane, and nylon into molds and heating and sintering them at high temperatures to form porous bodies with micropores. However, it is well known that the porous body is then manufactured by a so-called sintering method in which the porous body is impregnated with ink. However, in the case where polymer powders as mentioned above are simply integrated by sintering, a large amount of heat is required for sintering, and it is difficult to obtain the desired porosity, and it is difficult to achieve the desired ink impregnation rate. This method has the disadvantage that it is not possible to produce a porous body that is strong and has appropriate elasticity and has excellent ink exudation properties. It is also known that inorganic or organic fine powder particles are coated with thermoplastic elastomer on the entire surface and then sintered to obtain a porous body, which is then impregnated with ink (Japanese Patent Application Laid-Open No. (See Publication No. 53-23357). However, this type also had the same drawbacks as the previous type, and the vacancy rate was still low. The present invention has been completed in order to eliminate the above-mentioned drawbacks, and its gist is that inorganic powder particles are formed by a large number of fine particles of an organic elastic material attached to the outer peripheral surface at intervals. The present invention is an ink-impregnated body in which a continuous porous body is formed by using the organic elastic material as a framework material, and the framework materials are mutually fixed by fine particles of the organic elastic material, and the ink is impregnated with the continuous porous body. The ink-impregnated body of the present invention has a structure in which inorganic powder particles are fixed to each other by organic elastic material fine particles, and has superior toughness, abrasion resistance, and porosity compared to conventional ones, and can absorb ink. It has good durability for replenishing ink ribbons or type. Inorganic powders used in the present invention include, for example, soft inorganic powders with excellent compression properties such as carbon black, calcium carbonate, and calcium sulfite, hard inorganic powders with excellent tensile strength such as silica, aluminum silicate, and clay, and titanium powders. Potassium acid, wollastonite, talc, mica, etc., which increase tensile strength and compressive properties, can be mentioned. Examples of materials for the organic elastic material fine particles in the present invention include thermoplastic resins, thermoplastic rubbers, thermosetting resins, and reactive liquid rubbers. Examples of the thermoplastic resin include polyvinyl chloride, polyethylene, polypropylene, polyethylene terephthalate, polybutylene terephthalate, polyamide, and polyamide copolymer. Examples of the thermoplastic rubber include polyurethane and acrylonitrile-butadiene rubber. These thermoplastic resins and thermoplastic rubbers are attached in a molten state. Examples of thermosetting resins include polyurethane, epoxy resins, unsaturated polyesters, and diallyl phthalate resins, and examples of reactive liquid rubbers include liquid urethane rubber, liquid butadiene-styrene rubber, and liquid acrylonitrile-butadiene rubber. , liquid chloroprene rubber, etc. Both of these thermosetting resins and reactive liquid rubbers are liquefied or liquefied at relatively low temperatures. Next, a method of manufacturing a skeleton material by attaching organic elastic material fine particles to the outer surface of the inorganic powder particles and a method of molding the obtained skeleton material will be explained. The organic elastic material is in a liquid state and is mixed with the inorganic powder so that it adheres to the surface of the inorganic powder particles with some spacing, and a large number of fine organic elastic material particles adhere to the outer surface of the inorganic powder particles at intervals. Obtain the framework material for the structure. FIG. 1 is a schematic cross-sectional view showing an example of a skeleton material obtained in this manner, in which a large number of organic elastic material fine particles 2 are attached to inorganic powder particles 1 with gaps between the particles. This makes it possible to greatly increase the porosity of the resulting porous material, and furthermore, by appropriately changing the amount of organic elastic material mixed, it is possible to obtain a porous material with a desired porosity. The advantages are demonstrated. The inorganic powder particles 1 preferably have a particle size of 5 to 150 μm and are spherical or nearly spherical (for example, ellipsoidal). The framework material in which the organic elastic material fine particles 2 are attached to the inorganic powder particles 1 in this way is uniformly filled into the mold by a pressureless filling method using a vibrator, and the porous material is sintered by heat treatment with hot air. You can gain a healthy body. Thus, the present invention has the advantage that the amount of heat required for sintering can be extremely reduced. The organic elastic material is attached to the surface of the inorganic powder particles with gaps between the particles, and the framework materials are bonded to each other by thermoforming and impart elasticity. The organic elastic material may be mixed with an inorganic powder in a liquid state and then filled into a mold, or the materials may be placed in a mold and mixed together. When a thermoplastic resin is used as the organic elastic material, the thermoplastic resin is heated and molten and mixed with an inorganic powder, and then cooled and solidified in a mold. In addition, liquid thermosetting resin undergoes polycondensation by heating and forming in a mold.
After being cured, the reactive liquid rubber is likewise crosslinked and cured by heat treatment in the mold. The blending amount of the organic elastic material will be changed as appropriate depending on the type of material used, but it should be 10 to 50% (wt%, same hereinafter), especially 20 to 35% of the total amount of inorganic powder and organic elastic material. % is preferred. In order to improve the adhesion between the inorganic powder and the organic elastic material, titanate coupling agents such as isopropyl tri(dioctyl phosphate) titanate and isopropyl triisostearoyl titanate, as well as silane coupling agents, zirconate coupling agents, and aluminum are used. It is preferable to use a coupling agent such as a calcium-based coupling agent or a calcium-based coupling agent. Such coupling agents improve the surface adhesion of inorganic powders,
It imparts strong adhesive strength, acts as a viscosity modifier for liquid organic elastic materials, and also functions as a curing catalyst. The shape of the inorganic powder in the present invention is spherical,
Various shapes such as fibrous shape and plate shape (flake shape) are preferably employed. For example, if the inorganic powder is approximately spherical, the powder particles in the mold are arranged as shown in Figure 2 by the non-pressure filling method using a vibrator (for example, the parallel rhombus filling method) as described above. However,
In the present invention, as shown in FIG. 1, the organic elastic material fine particles 2 are attached to the surface with appropriate spacing, resulting in an arrangement as shown in FIG. 3, which greatly increases the porosity. can do. Incidentally, in the arrangement shown in FIG. 2, the porosity is about 25% by volume, but in the arrangement shown in FIG. 3, it is possible to increase the porosity to 60-75% by volume. If the inorganic powder is in the form of short fibers (for example, monocrystalline fibers such as potassium titanate or wollastonite, with an aspect ratio of 10 to 50:1 and a diameter of 15 to 30μ), the strength will be increased uniaxially when blended. However, by filling the mold without orientation, the void can be enlarged.
In addition, inorganic short fibers include organic short fibers (for example, aromatic polyamide fibers such as Kevlar fiber manufactured by DuPont),
It is preferable to use a mixture of carbon fibers, graphite fibers, polyester fibers, etc., in order to increase toughness. In addition, plate-like powder (such as kaolin and talc, typically mica, which has a width
When the flake aspect ratio is 1.4 to 4μ and 40μ or less, usually 2 to 3μ, and the flake aspect ratio is 4:1 to 100:1, it is also non-oriented or uniaxially oriented, as in the case of short fibers. Just fill it into the mold. Furthermore, by using inorganic powders having each of these shapes in combination, the porosity can be increased. In the present invention, after filling a mold with a framework material in which organic elastic material fine particles are attached to inorganic powder particles, the organic elastic material fine particles are rapidly melted and sintered, and either cooled and solidified or heated and hardened. In order to shorten the processing time, it is preferable to preheat by far-infrared irradiation or the like. After heat molding, the resulting porous body can be treated with alcohol, acetone, benzene, etc. to dissolve the organic elastic material.
Micropores are formed by removing or shrinking the thin film on the surface of the porous material by immersing it in a mixed solution of a solvent such as xylene or dimethylformamide and a non-solvent such as water, or preferably by contacting it with the magnetism of these solvents. It is preferable to open it and aim for uniform porous formation. For impregnating the thus obtained porous body with ink, an ink impregnation method used for ordinary ink pads and ink rolls can be suitably employed. As described above, the present invention uses inorganic powder etc. to create a framework material having a structure in which fine particles of an organic elastic material are attached to the outer surface of inorganic powder particles which can take various shapes with gaps between the particles. It is firmly bonded by short-time heating and pressure forming under much lower temperature conditions than normal sintering conditions, and has the toughness, wear resistance, and dimensional stability of inorganic powder. It has the excellent advantage of being able to easily produce a porous body having excellent properties such as, and having cavities of a size suitable for an ink roll or an ink pad. Next, the present invention will be explained with reference to Examples. Example 1 While stirring spherical calcium sulfite powder with an average particle size of 5 μm in a high-shear stirrer, molten nylon 66 was atomized at a ratio of 20% of the total amount to the outside of the calcium sulfite powder particles. The droplets were deposited on the surface with gaps between them and then cooled. The obtained adhering calcium sulfite powder was struck and vibrated with a ribbon blender to sufficiently loosen the agglomerated powder, and then a predetermined amount was filled into a mold with a diameter of 20 mmφ and a length of 40 mm, and the powder was heated under pressure. It was heat-molded at 200°C for 5 minutes and then allowed to cool to obtain a porous body. This material was impregnated with oil-based ink to obtain an ink-impregnated body. Example 2 While stirring spherical calcium sulfite powder with an average particle size of 10μ in a high-shear stirrer, liquid polyurethane [room-temperature curable polyurethane resin ADAPT60L]
Liquid polyurethane (manufactured by Kokusai Chemical Co., Ltd.) containing 10 parts by weight and 3 parts by weight of a curing agent (liquid isocyanate) was poured into a thread at a ratio of 15% of the total amount to the outer surface of the calcium sulfite powder particles. The droplets were deposited with a gap between them. The resulting adhered calcium sulfite powder was struck and vibrated with a ribbon blender to sufficiently loosen the agglomerated powder, and then a predetermined amount was filled into a mold with a diameter of 25 mmφ and a length of 50 mm, and heated at 100°C.
A porous body was obtained by heating and molding for 5 minutes. This material was impregnated with oil-based ink to obtain an ink-impregnated body. Example 3 A reactive liquid rubber composition [Hiker CTBN 1300
(Nitrile rubber manufactured by Gutsudoritsuchi Chemical Co.)
143 parts by weight, 24 parts by weight of bisphenol A (chain extender), epoxy resin RA 10A (manufactured by Kokusai Chemical Co., Ltd.)
A composition containing 100 parts by weight of epoxy resin curing agent RA 10B (manufactured by Kokusai Chemical Co., Ltd.)]
was injected at a rate of 10% of the total amount using a quantitative mixing and dispensing machine, and the droplets were deposited on the outer surface of the calcium sulfite powder particles with gaps between the droplets. The obtained adhered calcium sulfite powder was prepared in Example 1.
In the same manner as above, it was loosened with a ribbon blender, filled into a mold, gelled at 40°C for 7.5 minutes, and further cured at room temperature for 30 minutes to obtain a porous body. This material was impregnated with oil-based ink to obtain an ink-impregnated body. Comparative example Filled with nylon 6 powder with an average particle size of 65μ,
After preheating and forming under pressure at 160℃ for 10 minutes,
The porous body obtained by firing in a hot atmosphere at 260° C. for 3 minutes was cooled and dried, and then impregnated with oil-based ink to obtain an ink-impregnated body. The toughness, abrasion resistance, and porosity of each ink-impregnated body obtained in Examples 1 to 3 and Comparative Example were examined. The results are shown in Table 1. The test items for each test item in Table 1 are as follows. (1) Toughness Tensile strength and elongation were based on the tensile test method described in JIS K 6301. In addition, the tensile stress was measured on the test piece (outer diameter 44.6 mmφ, inner diameter
36.6mmφ, length 57.5mm) by measuring the tensile load when 50% elongation was applied. (2) Wear rate The degree of wear was measured in accordance with British standard BS 903 part A9C method. In other words, a load of 1.4 kg (3 pounds) was applied to a sample (thickness 10 mm, width 14 mm) using an Akron type abrasion tester, and the polishing disk was rotated with an inclination angle of 15 degrees between the sample and the rotating surface of the polishing disk. The wear rate was determined by measuring the abrasion weight. (3) Vacancy rate The vacancy rate was calculated using the following formula. (1-W/d×V)×100 W: Weight of porous body not containing ink V: Volume of porous body d: Specific gravity of porous body constituent material
【表】
またこれら実施例1〜3でえられたインク含浸
体はその微細孔内に含有されるインクの滲出性に
すぐれており、とくに微圧下でのインク滲出性に
すぐれていた。[Table] In addition, the ink-impregnated bodies obtained in Examples 1 to 3 were excellent in exudation of the ink contained in the fine pores, and were particularly excellent in ink exudation under slight pressure.
第1図は本発明における無機粉末粒子の外表面
に有機弾性材微粒子が付着している骨格材の一例
を示す概略断面図、第2図は球状の無機粉末粒子
のモールド内での配列を示す概略説明図、第3図
は第1図に示した骨格材のモールド内での配列を
示す概略断面図である。
(図面の符号)、1:無機粉末粒子、2:有機
弾性材微粒子。
Fig. 1 is a schematic cross-sectional view showing an example of a framework material in which organic elastic material fine particles are attached to the outer surface of inorganic powder particles in the present invention, and Fig. 2 shows an arrangement of spherical inorganic powder particles in a mold. The schematic explanatory drawing, FIG. 3, is a schematic cross-sectional view showing the arrangement of the framework material shown in FIG. 1 within the mold. (Symbols in drawings), 1: inorganic powder particles, 2: organic elastic material fine particles.
Claims (1)
配して多数付着されてなる無機粉末粒子が骨格材
とされ、前記有機弾性材の微粒子によつて、前記
骨格材が相互に固着されてなる連続多孔質体にイ
ンクが含浸されてなるインク含浸体。 2 前記無機粉末が、粒径5〜150μのものであ
る特許請求の範囲第1項記載のインク含浸体。 3 前記無機粉末が、球状またはそれに近いもの
である特許請求の範囲第1項または第2項記載の
インク含浸体。 4 前記無機粉末が、短繊維状である特許請求の
範囲第1項記載のインク含浸体。 5 骨格材として、さらに有機短繊維を混合して
なる特許請求の範囲第4項記載のインク含浸体。 6 前記無機粉末が、板状である特許請求の範囲
第1項記載のインク含浸体。 7 前記有機弾性材が、熱可塑性樹脂、熱可塑性
ゴム、熱硬化性ゴム、熱硬化性樹脂および反応性
液状ゴムよりなる群からえらばれた少なくとも1
種である特許請求の範囲第1項、第2項、第3
項、第4項、第5項または第6項記載のインク含
浸体。[Scope of Claims] 1. Inorganic powder particles having a large number of fine particles of an organic elastic material attached to the outer circumferential surface at intervals are used as a skeleton material, and the fine particles of the organic elastic material make the skeleton material An ink-impregnated body is formed by impregnating ink into a continuous porous body formed by mutually fixed porous bodies. 2. The ink-impregnated body according to claim 1, wherein the inorganic powder has a particle size of 5 to 150 μm. 3. The ink-impregnated body according to claim 1 or 2, wherein the inorganic powder is spherical or nearly spherical. 4. The ink-impregnated body according to claim 1, wherein the inorganic powder is in the form of short fibers. 5. The ink-impregnated body according to claim 4, further comprising organic short fibers as a skeleton material. 6. The ink-impregnated body according to claim 1, wherein the inorganic powder is plate-shaped. 7. The organic elastic material is at least one selected from the group consisting of thermoplastic resin, thermoplastic rubber, thermosetting rubber, thermosetting resin, and reactive liquid rubber.
Claims 1, 2, and 3 that are species
The ink-impregnated body according to item 1, 4, 5, or 6.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13467983A JPS5935968A (en) | 1983-07-22 | 1983-07-22 | Manufacture of ink holding porous body |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13467983A JPS5935968A (en) | 1983-07-22 | 1983-07-22 | Manufacture of ink holding porous body |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP7533481A Division JPS5939458B2 (en) | 1981-05-18 | 1981-05-18 | Manufacturing method of ink holding porous body |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5935968A JPS5935968A (en) | 1984-02-27 |
| JPH0216705B2 true JPH0216705B2 (en) | 1990-04-18 |
Family
ID=15134032
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP13467983A Granted JPS5935968A (en) | 1983-07-22 | 1983-07-22 | Manufacture of ink holding porous body |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5935968A (en) |
-
1983
- 1983-07-22 JP JP13467983A patent/JPS5935968A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5935968A (en) | 1984-02-27 |
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