JPH0250878B2 - - Google Patents
Info
- Publication number
- JPH0250878B2 JPH0250878B2 JP12283182A JP12283182A JPH0250878B2 JP H0250878 B2 JPH0250878 B2 JP H0250878B2 JP 12283182 A JP12283182 A JP 12283182A JP 12283182 A JP12283182 A JP 12283182A JP H0250878 B2 JPH0250878 B2 JP H0250878B2
- Authority
- JP
- Japan
- Prior art keywords
- printing
- blanket
- powder
- compressed layer
- rubber
- 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
- 238000000034 method Methods 0.000 claims description 19
- 239000000843 powder Substances 0.000 claims description 16
- 229920001971 elastomer Polymers 0.000 claims description 15
- 238000004519 manufacturing process Methods 0.000 claims description 14
- 239000004744 fabric Substances 0.000 claims description 13
- 239000005060 rubber Substances 0.000 claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 9
- 229920000642 polymer Polymers 0.000 claims description 9
- 238000009472 formulation Methods 0.000 claims description 8
- 239000003480 eluent Substances 0.000 claims description 6
- 239000002245 particle Substances 0.000 claims description 4
- 238000010030 laminating Methods 0.000 claims description 3
- 238000007645 offset printing Methods 0.000 claims description 3
- 238000007639 printing Methods 0.000 description 27
- 239000010410 layer Substances 0.000 description 23
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 229920002959 polymer blend Polymers 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 235000002639 sodium chloride Nutrition 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 206010040844 Skin exfoliation Diseases 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000007906 compression Methods 0.000 description 3
- 230000006835 compression Effects 0.000 description 3
- 239000000976 ink Substances 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 229920000459 Nitrile rubber Polymers 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- ZCCIPPOKBCJFDN-UHFFFAOYSA-N calcium nitrate Chemical compound [Ca+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ZCCIPPOKBCJFDN-UHFFFAOYSA-N 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000806 elastomer Substances 0.000 description 2
- 238000010828 elution Methods 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 239000004088 foaming agent Substances 0.000 description 2
- 230000003014 reinforcing effect Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
- 230000008961 swelling Effects 0.000 description 2
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 1
- WXHLLJAMBQLULT-UHFFFAOYSA-N 2-[[6-[4-(2-hydroxyethyl)piperazin-1-yl]-2-methylpyrimidin-4-yl]amino]-n-(2-methyl-6-sulfanylphenyl)-1,3-thiazole-5-carboxamide;hydrate Chemical compound O.C=1C(N2CCN(CCO)CC2)=NC(C)=NC=1NC(S1)=NC=C1C(=O)NC1=C(C)C=CC=C1S WXHLLJAMBQLULT-UHFFFAOYSA-N 0.000 description 1
- 241000473391 Archosargus rhomboidalis Species 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- SUAKHGWARZSWIH-UHFFFAOYSA-N N,N‐diethylformamide Chemical compound CCN(CC)C=O SUAKHGWARZSWIH-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- ZMXDDKWLCZADIW-UHFFFAOYSA-N dimethylformamide Substances CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 239000004005 microsphere Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 238000013040 rubber vulcanization Methods 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41N—PRINTING PLATES OR FOILS; MATERIALS FOR SURFACES USED IN PRINTING MACHINES FOR PRINTING, INKING, DAMPING, OR THE LIKE; PREPARING SUCH SURFACES FOR USE AND CONSERVING THEM
- B41N10/00—Blankets or like coverings; Coverings for wipers for intaglio printing
- B41N10/02—Blanket structure
- B41N10/04—Blanket structure multi-layer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41N—PRINTING PLATES OR FOILS; MATERIALS FOR SURFACES USED IN PRINTING MACHINES FOR PRINTING, INKING, DAMPING, OR THE LIKE; PREPARING SUCH SURFACES FOR USE AND CONSERVING THEM
- B41N2210/00—Location or type of the layers in multi-layer blankets or like coverings
- B41N2210/02—Top layers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41N—PRINTING PLATES OR FOILS; MATERIALS FOR SURFACES USED IN PRINTING MACHINES FOR PRINTING, INKING, DAMPING, OR THE LIKE; PREPARING SUCH SURFACES FOR USE AND CONSERVING THEM
- B41N2210/00—Location or type of the layers in multi-layer blankets or like coverings
- B41N2210/04—Intermediate layers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41N—PRINTING PLATES OR FOILS; MATERIALS FOR SURFACES USED IN PRINTING MACHINES FOR PRINTING, INKING, DAMPING, OR THE LIKE; PREPARING SUCH SURFACES FOR USE AND CONSERVING THEM
- B41N2210/00—Location or type of the layers in multi-layer blankets or like coverings
- B41N2210/10—Location or type of the layers in multi-layer blankets or like coverings characterised by inorganic compounds, e.g. pigments
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41N—PRINTING PLATES OR FOILS; MATERIALS FOR SURFACES USED IN PRINTING MACHINES FOR PRINTING, INKING, DAMPING, OR THE LIKE; PREPARING SUCH SURFACES FOR USE AND CONSERVING THEM
- B41N2210/00—Location or type of the layers in multi-layer blankets or like coverings
- B41N2210/14—Location or type of the layers in multi-layer blankets or like coverings characterised by macromolecular organic compounds
Landscapes
- Printing Plates And Materials Therefor (AREA)
Description
本発明は印刷用ブランケツトの製造方法、特に
圧縮層を有する印刷用ブランケツトの製造方法に
関するものである。
高速オフセツト印刷等に用いる印刷用ブランケ
ツトにおいては弾性重合体の圧縮層を設けること
が行なわれている。この圧縮層は第1に、印刷圧
力時にブランケツトの圧縮面に生ずる膨みを均一
に吸収し、ブランケツト表面の変形を減少させ、
鮮明な画像を得られるようにする働きがある。第
2に印刷用紙が折り曲げられて送られてきたり、
二枚以上重なつて送られたとき、この圧縮層が圧
縮することにより版銅やブランケツト表面に加わ
る力(印圧以外の力)を吸収し、緩和しえ、この
ため版胴、ブランケツト表面層の寿命を著しく改
良しえる。第3に胴仕立をする場合、一般のブラ
ンケツトにあつては非常に厳密な厚さ調整をしな
ければならないが圧縮層を設けることにより基準
胴仕立てよりも多少オーバー気味に仕立てても鮮
明な印刷を得ることが可能となり、作業者の熟練
度に関係なく胴仕立ができるという利点がある。
このような圧縮層を製造する方法としては、合
成ゴム配合物中に発泡剤を配合しておき、ゴム加
硫時に加熱発泡させて気泡を有する圧縮層を設け
る方法あるいは、多孔質フエルトにエラストマー
を含浸をさせる方法、また、中空微小球をエラス
トマー中に分散させ独立気泡を形成させ圧縮層と
する方法等が知られている。
印刷用ブランケツトの圧縮層は前述のような特
性、すなわちブランケツト表面に生ずる膨みを
均一に吸収すること、ブランケツト表面にかか
る力を緩和することを必要とすると共に高速印
刷時には、それに対応する応答速度で圧縮歪みを
回復しなければならないこと、さらに充分な耐
久性を有すること等と言う種々の特性を備えるこ
とを要求される。これに加え、印刷用ブランケツ
トは種々の印刷方法等により要求される性能も異
なるため、この圧縮層を製造する方法としては、
これらの要求を容易に充足させる方法であること
が望ましい。
これらの特性を充足する圧縮層としては、圧縮
性が2.0〜8.0Kg/cm2(1mm/分の圧縮速度、0.15
mm圧縮時の応力(以下同じ)であること、凝集力
が200g/cm〔ピーリング試験(以下同じ)〕以上
あること等が要求され、特に圧縮性においては印
刷方法等の相違により、種々の圧縮性を有するブ
ランケツトが必要である。
圧胴によつて加圧されるブランケツトに、この
加圧によつて剪断応力が働くことになるが、すく
なくとも凝集力が200g/cm以上ないと、この剪
断応力に耐えられないからである。
しかしながら、従来方法によれば、いずれも4
Kg/cm2未満の高度の圧縮性を有するブランケツト
を製造できず、多様性のある印刷用ブランケツト
を製造することや不可能であつた。
本発明はこのような欠点のない印刷用ブランケ
ツトの製造方法を提供すること、詳しくは圧縮性
として2.0〜8.0Kg/cm2の範囲を有し、また凝集力
として200g/cm以上を備えた印刷用ブランケツ
トを容易に製造しえ、かつ圧縮性において多様性
のある印刷用ブランケツトを簡単に製造しえる方
法を提供することを目的とする。
したがつて本発明による圧縮性2.0〜8.0Kg/
cm2、ピーリング強度200g/cm以上の圧縮層を有
する、印刷用ブランケツトの製造方法は、オフセ
ツト印刷用ブランケツトの圧縮層の製造方法にお
いて、下記の工程を含むことを特徴とするもので
ある。
a 耐油性ポリマーのゴム配合物に平均粒径10〜
50μmの、溶出液に溶解する粉体を、前記配合
物100重量部に対し70〜200重量部添加する工
程。
b この粉体を添加したa項の配合物を基布上に
300〜1000g/m2の割合で積層し加硫する工程。
c この積層体を両端部に10〜100Kg/m巾の張
力をかけて、60〜100℃の温度範囲の溶出液に
浸漬する工程。
本発明による印刷用ブランケツトの製造方法に
よれば、凝集力200g/cm以上で、圧縮性が2.0〜
8.0Kg/cm2の範囲の、任意の圧縮性を示すブラン
ケツトを粉体添加量、前記配合物溶液塗布量、溶
出条件等を制御することにより、容易に得ること
ができると言う利点がある。
本発明を更に詳しく説明する。
本発明による印刷用ブランケツトの製造方法に
よれば、耐油性ポリマーのゴム配合物に溶出液に
溶出されうる粉体を添加する。
耐油性ポリマーのゴム配合物は圧縮層本体とな
るものであり、印刷用ブランケツトであるために
印刷用インク、インク替えの際使用する溶剤等に
抵抗力があることが要求され、このため耐油性の
ものを用いる必要がある。このような配合に使用
するポリマーとしては、たとえばポリ塩化ビニ
ル、クロロプレンゴム、ニトリルゴム、多硫化ゴ
ム、ポリウレタン、フツ素系ゴム、アクリルゴ
ム、ヒドリンゴム等の1種以上であることができ
る。このような耐油性ポリマーの配合物はこの主
要成分のゴム等に硫黄等の加硫剤、加硫促進剤、
カーボンブラツク等の補強剤、老化防止剤及びス
テアリン酸等の加工剤等の1種以上を添加したも
のであつてもよい。
このポリマーの配合物は通常、溶解して用いら
れるが、この溶剤としては、ポリマーの配合物を
溶解するものであれば基本的にいかなるものでも
よい。たとえば、N−N′−ジメチルホルムアミ
ド、ジエチルホルムアミド、ジメチルアセトアミ
ド、ジメチルスルホキシド、トルエン、MEK、
MIBK等の1種以上であることができる。
このポリマーの配合物に添加する粉体は前述の
ように、溶出液に溶出可能なものであればいかな
るものでもよい。たとえば炭酸ナトリウム、重炭
酸ソーダ、重炭酸カリウム、塩化ナトリウム、硝
酸ナトリウム、硝酸カルシウム等の無機塩、砂糖
殿粉等の水溶性有機物、フエノール、スルホサリ
チル酸、酒石酸等の有機酸ないし、これらの塩等
の一種以上であることができる。
この粉体の平均粒径は10〜50μmである。50μ
mより大きいと大きい空孔となり均一かつ凝集力
の大きい圧縮層にならない一方、10μmより小さ
いと、抽出時間が長く必要になり分散不良のため
均一な圧縮層になりがたく圧縮層を保持しがた
い。
また、粉体の添加量は記ポリマーの配合物100
重量部に対し、70〜200重量部である。70重量部
未満であると圧縮応力が、4.0Kg/cm2を超えてし
まい、200重量部より多いと、2.0Kg/cm2より小さ
くなつてしまい。印刷時のインキ転移に必要な圧
力が得られないと共に凝集力が不足し、印刷時の
剪断力により剥離現像を起こす原因となる。
この粉体のポリマーの配合物への添加方法は基
本的に限定されるものではない。たとえば、開放
型のミキシングロール、密閉型混合機(バンバリ
ーミキサー、加圧ニーダ等)を用いることがで
き、ポリマーの配合物を溶液とした場合には、撹
拌混合機を用いポリマーの配合物中に均一分散さ
せる。
この粉体を添加したポリマーの配合物を基布上
に積層するわけであるが、この基布は基本的にい
かなるものでもよい。たとえば、綿布、レーヨン
布、ポリエステル布等であることができる。
このような基布上に粉体を添加したポリマーの
配合物を積層する方法も限定されるものではなく
カレンダリングにより貼り合わせてもよく、押し
出しフイルムを積層してもよい。また溶液として
用いる場合は、ナイフコータ、ロールコータ等に
より塗布積層しえる。
この積層の割合は300〜1000g/cm2である。300
g/m2より少ないと圧縮性が4.0Kg/cm2以下にな
らない。また1000g/cm2より多いと、ブランケツ
トの製品厚さの制約により、表面ゴム層、補強基
布層の必要な厚さを確保出来なくなる。
このような積層体を任意に加硫した後、溶出液
中に浸漬する。この際、溶出液の温度は60〜100
℃である。室温より低いと、粉体の溶出に時間が
かかりすぎ結果としてゴムの特性が損なわれる恐
れを生じ、100℃をこえると、配合物の抽出も併
せておこり、製品の耐久性に影響する。また浸漬
時間は3分〜6時間である。3分未満であると粉
体が充分溶出せず所望の圧縮応力のブランケツト
が得られないし、6時間を超えると、基布の特性
に変化をきたしまた、ゴム配合物の抽出もともな
つてくる。溶出液としては、たとえば、水、メタ
ノール、エタノール等のモノオール類、グリセリ
ン、エチレングリコール等のポリオール類等の1
種以上が用いられる。
この溶出液への浸漬に際しては、積層体1両端
部をロール2,2′(ガイドロール4,4を介し
て捲きつけ)、このロール2,2′を正逆に回転せ
しめ張力をかけながら、水3中に浸漬するのが好
ましい(第1図)。この積層体にかける張力は10
〜100(Kgm/巾m)であるのがよい。10Kg/m巾
より小さいと、しぼり効果が少くまた100(Kgm/
巾)より大きいと基布の強度低下につながる。こ
のしぼり効果は圧縮層のミクロセルを破壊して
連通孔を多くする、粉体と水が置換しやすく、
迅速な溶出が可能になり、圧縮層の特性を損なう
危険がない、ロール2,2′が正逆に回転せし
めるため、積層体がロール2,2′に捲回される
ときにしぼられて、脱水が容易になるため、粉体
の溶出が迄速に行なわれる、という作用がある。
すなわち、添加した粉体を確実に除去できること
になり、圧縮性の制御が容易になる。
このようにして製造された圧縮層上にゴム糊を
塗布し、補強布を積層し、その上に表面ゴム層等
を設け印刷用ブランケツトとする。
以下実施例について説明する。
例 1
常法通りに混練したニトリルゴムコンパウンド
をトルエンで溶解し、これに前記コンパウンドに
対し界面活性剤2部と平均粒径20μmの食塩150
部を投入し、均一に分散するように、良く混合撹
拌を行なつた。
これを綿布上にナイフコータを用いて、600
g/m2の割合で塗布し、溶剤を乾燥し、加硫した
後、80℃の水に4時間浸漬した。
これを例1と同様にして印刷用ブランケツトと
した。このブランケツトの圧縮応力は2.5Kg/cm2
であつた。
このときの圧縮応力及び従来の方法により製造
されたブランケツトの圧縮応力を表として示し
た。
The present invention relates to a method for manufacturing printing blankets, and in particular to a method for manufacturing printing blankets having a compressed layer. Printing blankets used for high-speed offset printing and the like are provided with a compressed layer of elastic polymer. This compressed layer firstly absorbs uniformly the swelling that occurs on the compressed surface of the blanket during printing pressure, reducing deformation of the blanket surface;
Its function is to make it possible to obtain clear images. Second, the printing paper is sent folded,
When two or more sheets are stacked and sent, this compressed layer absorbs and relieves the force (force other than printing pressure) applied to the plate cylinder and blanket surface by compressing, and therefore the plate cylinder and blanket surface layer can significantly improve the service life of Third, when tailoring the body, for ordinary blankets, the thickness must be adjusted very precisely, but by providing a compressed layer, even if the body is tailored a little over the standard body style, clear printing can be achieved. This has the advantage that the torso can be tailored regardless of the skill level of the worker. As a method for manufacturing such a compressed layer, there is a method in which a foaming agent is mixed into a synthetic rubber compound, and the foaming agent is heated and foamed during rubber vulcanization to form a compressed layer having air bubbles. Alternatively, an elastomer is applied to a porous felt. A method of impregnation and a method of dispersing hollow microspheres in an elastomer to form closed cells to form a compressed layer are known. The compressed layer of a printing blanket needs to have the above-mentioned characteristics, namely, to uniformly absorb the swelling that occurs on the blanket surface, to relieve the force applied to the blanket surface, and to have a corresponding response speed when printing at high speeds. It is required to have various properties such as the need to recover from compressive strain and sufficient durability. In addition, printing blankets have different performance requirements depending on various printing methods, so the methods for manufacturing this compressed layer include:
It is desirable to have a method that easily satisfies these requirements. A compressed layer that satisfies these characteristics has a compressibility of 2.0 to 8.0 Kg/cm 2 (compression speed of 1 mm/min, 0.15
mm compression stress (hereinafter the same), cohesive force must be 200 g/cm or more [peeling test (hereinafter the same)], etc. Especially in compressibility, due to differences in printing methods etc., various compression We need a blanket that has the properties of This is because the blanket pressurized by the impression cylinder will be subjected to shear stress due to this pressurization, but unless the cohesive force is at least 200 g/cm or more, it will not be able to withstand this shear stress. However, according to the conventional method, both
It has not been possible to produce blankets with high compressibility of less than Kg/cm 2 and it has been impossible to produce printing blankets with versatility. The object of the present invention is to provide a method for producing a printing blanket free from such drawbacks, and more specifically, to provide a printing blanket having a compressibility in the range of 2.0 to 8.0 kg/cm 2 and a cohesive force of 200 g/cm or more. It is an object of the present invention to provide a method for easily manufacturing printing blankets and for easily manufacturing printing blankets having various compressibility. Therefore, the compressibility according to the present invention is 2.0 to 8.0 kg/
cm 2 and having a compressed layer with a peeling strength of 200 g/cm or more, the method for manufacturing a compressed layer of an offset printing blanket is characterized by including the following steps. a Rubber compound of oil-resistant polymer with an average particle size of 10~
A step of adding 70 to 200 parts by weight of a powder of 50 μm that is soluble in the eluate to 100 parts by weight of the formulation. b. Apply the formulation of item a to which this powder is added on the base fabric.
A process of laminating and vulcanizing at a rate of 300 to 1000 g/ m2 . c. A step of applying a tension of 10 to 100 Kg/m width to both ends of this laminate and immersing it in an eluent having a temperature range of 60 to 100°C. According to the method for manufacturing a printing blanket according to the present invention, the cohesive force is 200 g/cm or more and the compressibility is 2.0 to 2.0.
There is an advantage that a blanket exhibiting any compressibility in the range of 8.0 Kg/cm 2 can be easily obtained by controlling the amount of powder added, the amount of the compound solution applied, elution conditions, etc. The present invention will be explained in more detail. According to the method for producing printing blankets according to the invention, a powder that can be eluted in an eluent is added to a rubber compound of an oil-resistant polymer. The rubber compound of oil-resistant polymer is the main body of the compressed layer, and since it is a printing blanket, it is required to be resistant to printing inks and solvents used when changing ink. It is necessary to use the following. The polymer used in such a formulation may be one or more of polyvinyl chloride, chloroprene rubber, nitrile rubber, polysulfide rubber, polyurethane, fluorine rubber, acrylic rubber, hydrin rubber, and the like. Such oil-resistant polymer formulations are made by adding vulcanizing agents such as sulfur, vulcanization accelerators, etc. to the main components such as rubber.
One or more of reinforcing agents such as carbon black, anti-aging agents, and processing agents such as stearic acid may be added. This polymer blend is usually used after being dissolved, and the solvent may basically be any solvent as long as it dissolves the polymer blend. For example, N-N'-dimethylformamide, diethylformamide, dimethylacetamide, dimethylsulfoxide, toluene, MEK,
It can be one or more types such as MIBK. As mentioned above, the powder added to the polymer formulation may be any powder as long as it can be eluted into the eluent. For example, inorganic salts such as sodium carbonate, sodium bicarbonate, potassium bicarbonate, sodium chloride, sodium nitrate, calcium nitrate, water-soluble organic substances such as sugar starch, organic acids such as phenol, sulfosalicylic acid, tartaric acid, etc., or one of these salts. It can be more than that. The average particle size of this powder is 10 to 50 μm. 50μ
If the pores are larger than m, the pores become large and a compressed layer with a uniform and strong cohesive force cannot be formed.If the diameter is smaller than 10 μm, a long extraction time is required, and due to poor dispersion, it is difficult to form a uniform compressed layer, making it difficult to maintain the compressed layer. sea bream. In addition, the amount of powder added is 100%
It is 70 to 200 parts by weight. If it is less than 70 parts by weight, the compressive stress will exceed 4.0 Kg/cm 2 , and if it is more than 200 parts by weight, it will be less than 2.0 Kg/cm 2 . The pressure required for ink transfer during printing cannot be obtained and cohesive force is insufficient, causing peeling development due to shearing force during printing. The method of adding this powder to the polymer formulation is essentially not limited. For example, an open-type mixing roll or a closed-type mixer (Banbury mixer, pressure kneader, etc.) can be used, and when a polymer blend is made into a solution, a stirring mixer can be used to dissolve the polymer blend. Distribute uniformly. This powder-added polymer blend is laminated onto a base fabric, and this base fabric may basically be of any type. For example, it can be cotton cloth, rayon cloth, polyester cloth, etc. The method of laminating the powder-added polymer blend on such a base fabric is not limited, and may be laminated by calendering, or extruded film may be laminated. When used as a solution, it can be coated and laminated using a knife coater, roll coater, or the like. The ratio of this lamination is 300 to 1000 g/cm 2 . 300
If it is less than g/m 2 , the compressibility will not be less than 4.0 Kg/cm 2 . Moreover, if it exceeds 1000 g/cm 2 , the required thickness of the surface rubber layer and reinforcing base fabric layer cannot be secured due to restrictions on the product thickness of the blanket. After optionally vulcanizing such a laminate, it is immersed in an eluent. At this time, the temperature of the eluate is 60 to 100.
It is ℃. If the temperature is lower than room temperature, it will take too long for the powder to dissolve, which may result in loss of rubber properties, and if it exceeds 100°C, extraction of the compound will also occur, which will affect the durability of the product. Moreover, the immersion time is 3 minutes to 6 hours. If the time is less than 3 minutes, the powder will not be sufficiently eluted and a blanket with the desired compressive stress cannot be obtained; if it is more than 6 hours, the properties of the base fabric will change and the rubber compound will be extracted. . Examples of eluents include water, monools such as methanol and ethanol, and polyols such as glycerin and ethylene glycol.
More than one species is used. When immersing in this eluate, both ends of the laminate 1 are wound around the rolls 2, 2' (wound through guide rolls 4, 4), and the rolls 2, 2' are rotated in forward and reverse directions while applying tension. Preferably, it is immersed in water 3 (FIG. 1). The tension applied to this laminate is 10
~100 (Kgm/width m) is preferable. If the width is smaller than 10Kg/m, the squeezing effect will be less and 100 (Kgm/m)
Width) larger than this will lead to a decrease in the strength of the base fabric. This squeezing effect destroys the microcells in the compressed layer and increases the number of communicating pores, making it easier for powder and water to replace each other.
Since the rolls 2, 2' rotate in forward and reverse directions, which allows rapid dissolution and no risk of impairing the properties of the compressed layer, the laminate is squeezed as it is wound around the rolls 2, 2'. Since dehydration is facilitated, the elution of the powder is accelerated.
That is, the added powder can be reliably removed, and compressibility can be easily controlled. Rubber paste is applied onto the compressed layer thus produced, a reinforcing cloth is laminated thereon, and a surface rubber layer etc. are provided thereon to obtain a printing blanket. Examples will be described below. Example 1 A nitrile rubber compound kneaded in a conventional manner is dissolved in toluene, and 2 parts of surfactant and 150 parts of common salt with an average particle size of 20 μm are added to the compound.
of the mixture and stirred well to ensure uniform dispersion. Apply this onto cotton cloth using a knife coater,
g/m 2 , dried the solvent, vulcanized, and then immersed in water at 80° C. for 4 hours. This was made into a printing blanket in the same manner as in Example 1. The compressive stress of this blanket is 2.5Kg/cm 2
It was hot. The compressive stress at this time and the compressive stress of the blanket manufactured by the conventional method are shown in a table.
【表】
以上説明したように、本発明による印刷用ブラ
ンケツトの製造方法によれば、凝集力が200g/
cm以上で、かつ圧縮応力が2.0〜8.0Kg/cm2のブラ
ンケツトが多様性をもつて製造しえる。特に、従
来製造しえなかつた4.0Kg/cm2未満の高度の圧縮
性を有するブランケツトが製造しえ、網点、調子
再現性等の印刷再現性のよいブランケツトを提供
しえると言う利点がある。[Table] As explained above, according to the printing blanket manufacturing method of the present invention, the cohesive force is 200g/
A wide variety of blankets can be produced with a compressive stress of 2.0 to 8.0 Kg/cm 2 . In particular, it has the advantage of being able to manufacture a blanket with a high degree of compressibility of less than 4.0 kg/cm 2 , which was previously impossible to manufacture, and providing a blanket with good printing reproducibility such as halftone dots and tone reproducibility. .
第1図は本発明の浸漬工程の一例を示す概略図
である。
1……積層体、2……ロール、3……水。
FIG. 1 is a schematic diagram showing an example of the dipping process of the present invention. 1...Laminated body, 2...Roll, 3...Water.
Claims (1)
造方法において、下記の工程を含むことを特徴と
する印刷用ブランケツトの圧縮層の製造方法。 a 耐油性ポリマーのゴム配合物に平均粒径10〜
50μmの、溶出液に溶解する粉体を、前記配合
物100重量部に対し70〜200重量部添加する工
程。 b この粉体を添加したa項の配合物を基布上に
300〜1000g/m2の割合で積層し加硫する工程。 c この積層体を両端部に10〜100Kg/m巾の張
力をかけて、60〜100℃の温度範囲の溶出液に
浸漬する工程。[Scope of Claims] 1. A method for producing a compressed layer for an offset printing blanket, the method comprising the following steps: a Rubber compound of oil-resistant polymer with an average particle size of 10~
A step of adding 70 to 200 parts by weight of a powder of 50 μm that is soluble in the eluate to 100 parts by weight of the formulation. b. Apply the formulation of item a to which this powder is added on the base fabric.
A process of laminating and vulcanizing at a rate of 300 to 1000 g/ m2 . c. A step of applying a tension of 10 to 100 Kg/m width to both ends of this laminate and immersing it in an eluent having a temperature range of 60 to 100°C.
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12283182A JPS5914995A (en) | 1982-07-16 | 1982-07-16 | Preparation of printing blanket |
| FR8311746A FR2530189B1 (en) | 1982-07-16 | 1983-07-13 | METHOD FOR MANUFACTURING A COMPRESSIBLE LAYER AND A BLANKET FOR PRINTING OPERATIONS |
| DE19833325595 DE3325595A1 (en) | 1982-07-16 | 1983-07-15 | COMPRESSIBLE LAYER FOR A RUBBER SCARF OF A PRINTING MACHINE AND METHOD FOR THEIR PRODUCTION |
| NL8302545A NL187344B (en) | 1982-07-16 | 1983-07-15 | METHOD FOR MANUFACTURING A COMPRESSIBLE LAYER OF A PRINTING FABRIC |
| CA000432572A CA1192099A (en) | 1982-07-16 | 1983-07-15 | Method of producing a compressible layer and a blanket for printing operation |
| GB8319180A GB2125315B (en) | 1982-07-16 | 1983-07-15 | Method of producing a compressible layer and of producing a blanket for use in printing |
| US06/515,310 US4422895A (en) | 1982-07-16 | 1983-07-18 | Method of producing a compressible layer and a blanket for printing operation |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12283182A JPS5914995A (en) | 1982-07-16 | 1982-07-16 | Preparation of printing blanket |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5914995A JPS5914995A (en) | 1984-01-25 |
| JPH0250878B2 true JPH0250878B2 (en) | 1990-11-05 |
Family
ID=14845717
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP12283182A Granted JPS5914995A (en) | 1982-07-16 | 1982-07-16 | Preparation of printing blanket |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5914995A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0641236B2 (en) * | 1985-11-27 | 1994-06-01 | 株式会社明治ゴム化成 | Printing blanket and manufacturing method thereof |
| JPH07428B2 (en) * | 1986-09-25 | 1995-01-11 | 株式会社明治ゴム化成 | Method for forming print surface shape in printing blanket |
| JPH0621734Y2 (en) * | 1987-10-07 | 1994-06-08 | 住友ゴム工業株式会社 | Offset blanket |
-
1982
- 1982-07-16 JP JP12283182A patent/JPS5914995A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5914995A (en) | 1984-01-25 |
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