JPH045089A - Desensitizing treatment solution of planographic printing plate and preparation thereof - Google Patents
Desensitizing treatment solution of planographic printing plate and preparation thereofInfo
- Publication number
- JPH045089A JPH045089A JP10701990A JP10701990A JPH045089A JP H045089 A JPH045089 A JP H045089A JP 10701990 A JP10701990 A JP 10701990A JP 10701990 A JP10701990 A JP 10701990A JP H045089 A JPH045089 A JP H045089A
- Authority
- JP
- Japan
- Prior art keywords
- acid
- phytic acid
- treatment solution
- desensitizing treatment
- desensitizing
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000007639 printing Methods 0.000 title claims abstract description 29
- IMQLKJBTEOYOSI-GPIVLXJGSA-N Inositol-hexakisphosphate Chemical compound OP(O)(=O)O[C@H]1[C@H](OP(O)(O)=O)[C@@H](OP(O)(O)=O)[C@H](OP(O)(O)=O)[C@H](OP(O)(O)=O)[C@@H]1OP(O)(O)=O IMQLKJBTEOYOSI-GPIVLXJGSA-N 0.000 claims abstract description 24
- IMQLKJBTEOYOSI-UHFFFAOYSA-N Phytic acid Natural products OP(O)(=O)OC1C(OP(O)(O)=O)C(OP(O)(O)=O)C(OP(O)(O)=O)C(OP(O)(O)=O)C1OP(O)(O)=O IMQLKJBTEOYOSI-UHFFFAOYSA-N 0.000 claims abstract description 24
- 229940068041 phytic acid Drugs 0.000 claims abstract description 24
- 235000002949 phytic acid Nutrition 0.000 claims abstract description 23
- 239000000467 phytic acid Substances 0.000 claims abstract description 23
- 239000000243 solution Substances 0.000 claims abstract description 17
- 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 claims abstract description 8
- 239000007864 aqueous solution Substances 0.000 claims abstract description 8
- 239000000203 mixture Substances 0.000 claims abstract description 6
- 239000002738 chelating agent Substances 0.000 claims abstract description 5
- 239000007788 liquid Substances 0.000 claims description 17
- 238000000586 desensitisation Methods 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 229910021645 metal ion Inorganic materials 0.000 abstract description 9
- 229910052751 metal Inorganic materials 0.000 abstract description 7
- 239000002184 metal Substances 0.000 abstract description 7
- 150000003839 salts Chemical class 0.000 abstract description 7
- 238000013329 compounding Methods 0.000 abstract description 3
- 238000010186 staining Methods 0.000 abstract 1
- 239000002253 acid Substances 0.000 description 15
- 239000013522 chelant Substances 0.000 description 10
- 238000000034 method Methods 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical class C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 6
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 6
- -1 etc.) Inorganic materials 0.000 description 5
- 239000011701 zinc Substances 0.000 description 5
- 229910052725 zinc Inorganic materials 0.000 description 5
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 4
- 238000007645 offset printing Methods 0.000 description 4
- 229960004889 salicylic acid Drugs 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000004480 active ingredient Substances 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000004020 conductor Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 239000005711 Benzoic acid Substances 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 230000002159 abnormal effect Effects 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 150000001555 benzenes Chemical class 0.000 description 2
- 235000010233 benzoic acid Nutrition 0.000 description 2
- 238000004945 emulsification Methods 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 230000003595 spectral effect Effects 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- QGKMIGUHVLGJBR-UHFFFAOYSA-M (4z)-1-(3-methylbutyl)-4-[[1-(3-methylbutyl)quinolin-1-ium-4-yl]methylidene]quinoline;iodide Chemical compound [I-].C12=CC=CC=C2N(CCC(C)C)C=CC1=CC1=CC=[N+](CCC(C)C)C2=CC=CC=C12 QGKMIGUHVLGJBR-UHFFFAOYSA-M 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000004375 Dextrin Substances 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
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical class CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004373 Pullulan Substances 0.000 description 1
- 229920001218 Pullulan Polymers 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-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
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910001413 alkali metal ion Inorganic materials 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 230000009920 chelation Effects 0.000 description 1
- BFGKITSFLPAWGI-UHFFFAOYSA-N chromium(3+) Chemical compound [Cr+3] BFGKITSFLPAWGI-UHFFFAOYSA-N 0.000 description 1
- JAWGVVJVYSANRY-UHFFFAOYSA-N cobalt(3+) Chemical compound [Co+3] JAWGVVJVYSANRY-UHFFFAOYSA-N 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052755 nonmetal Inorganic materials 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- 150000004986 phenylenediamines Chemical class 0.000 description 1
- VVOPUZNLRVJDJQ-UHFFFAOYSA-N phthalocyanine copper Chemical compound [Cu].C12=CC=CC=C2C(N=C2NC(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2N1 VVOPUZNLRVJDJQ-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- 235000019423 pullulan Nutrition 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明は、平版印刷版の不感脂化処理液に関し、更に詳
しくは、紙等の支持体表面に導電性の酸化亜鉛を塗布し
た版材(以下「マスターペーパー」と称する。)に、電
子写真法で親油性画像を形成し、こわを平版印刷版(オ
フセット印刷用原版)として使用する際に用いるフィチ
ン酸をキレート剤とした不惑脂化処理液およびその製造
方法の改良に関する。[Detailed Description of the Invention] <Industrial Application Field> The present invention relates to a desensitizing treatment liquid for lithographic printing plates, and more specifically to plate materials in which conductive zinc oxide is coated on the surface of a support such as paper. (hereinafter referred to as "master paper"), a lipophilic image is formed by electrophotography, and the stiffness is made into an unfathomable chelating agent using phytic acid, which is used as a lithographic printing plate (original plate for offset printing). This invention relates to improvements in processing liquids and methods for producing the same.
以下の説明で配合単位は、特にことわらない限り、重量
単位である。In the following description, the compounding unit is a weight unit unless otherwise specified.
〈従来の技術〉
オフセット印刷用電子写真版の不感脂化処理液には、(
ア)無害である、(イ)インクにシアニンブルー(フタ
ロシアニン銅キレート)を使用できる、(つ) pH調
整が容易である等の見地からフェロシアン錯塩を主体と
したものに代りフィチン酸を主体としたものになりつつ
ある。<Prior art> The desensitizing treatment liquid for electrophotographic plates for offset printing contains (
A) It is harmless, (b) Cyanine blue (phthalocyanine copper chelate) can be used in the ink, and (ii) pH adjustment is easy. It is becoming something like that.
そして、フィチン酸のキレート化機能を向上させた技術
として、例えば、特開平1−160691号公報で提案
されているものがある。下記に特許請求の範囲の欄の記
載を抽出する。As a technique for improving the chelating function of phytic acid, for example, there is a technique proposed in Japanese Patent Application Laid-open No. 1-160691. The description in the claims column is extracted below.
「それぞれ下記配合物からなる成分(^)、(B)、
(C) :
(A)フィチン酸、又は機能的訪導体、(B)二塩基酸
、又はその金属塩、および、(C)下記一般式(I)の
化合物又は、その水和物MXf 、
CI)[但し上式中Mは、二価の金属原子を表わし
、Xは一価又は二価の陰イオンを表わし、Lは1又は2
の整数を表わす]、
を有効成分として含有する平版印刷版不感脂化処理用組
成物、」
〈発明が解決しようとする課題〉
しかし、上記構成の不感脂化処理液は、不感脂化効果は
相当に高いが、水に難溶性の塩を生成しやすい金属イオ
ンを含んでいるため、作業環境の状況により従来のフェ
ロシアン系の不感脂化処理液が混入したりすると、金属
イオンは水不溶性のフェロシアン錯塩になったり、水可
溶性キレートから水不溶性キレートに変化して沈殿物を
生成するおそれがあった。“Ingredients (^), (B) each consisting of the following formulations,
(C): (A) phytic acid or a functional conductor, (B) a dibasic acid or a metal salt thereof, and (C) a compound of the following general formula (I) or a hydrate thereof MXf,
CI) [However, in the above formula, M represents a divalent metal atom, X represents a monovalent or divalent anion, and L represents 1 or 2
[representing an integer of ], a lithographic printing plate desensitization treatment composition containing as an active ingredient.''<Problem to be solved by the invention> However, the desensitization treatment liquid having the above structure has no desensitization effect. However, since it contains metal ions that tend to form salts that are sparingly soluble in water, if the conventional ferrocyane-based desensitization treatment solution is mixed into the working environment, the metal ions become water-insoluble. There was a risk that the water-soluble chelate might become a ferrocyane complex salt, or the water-soluble chelate might change to a water-insoluble chelate, forming a precipitate.
本発明は、上記にかんがみて、金属イオンを使用しなく
ても、大きな不感脂化効果が得られ、良好な安定性を有
する不感脂化処理液およびその製造方法を提供すること
を目的とする。In view of the above, it is an object of the present invention to provide a desensitizing treatment liquid that provides a large desensitizing effect and has good stability without using metal ions, and a method for producing the same. .
〈問題点を解決するための手段〉
本発明は、上記にかんがみてなされたものであり、キレ
ート剤としてフチン酸を用いる平版印刷版不感脂化処理
液およびその製造方法であって、水溶液中でフィチン酸
にスルホサルチル酸を作用させて錯体を形成させて、該
錯体を有効成分とするものである。<Means for Solving the Problems> The present invention has been made in view of the above, and provides a lithographic printing plate desensitization treatment solution using futic acid as a chelating agent and a method for producing the same, which comprises: A complex is formed by reacting phytic acid with sulfosalcylic acid, and the complex is used as an active ingredient.
く手段の詳細な説明〉 以下、上記手段について詳細に説明する。Detailed explanation of the method The above means will be explained in detail below.
(a)フィチン酸(別名、イノシトール六リン酸)は、
その2位−6位または3位−5位の水素基が、マスター
ベーパ上に電子写真法で形成された画像部以外の部分(
非画像部)の表面上の亜鉛をキレート化することにより
、該非画像部を疎油性としてインク(油性)の付着防止
作用を奏する。(a) Phytic acid (also known as inositol hexaphosphate) is
The hydrogen groups at the 2nd-6th or 3rd-5th positions are located on the master vapor in areas other than the image area formed by electrophotography (
By chelating zinc on the surface of the non-image area), the non-image area becomes oleophobic and has an effect of preventing ink (oil-based) from adhering.
なお、このフィチン酸は植物の種子あるいは穀物等から
得られる(工業的には米粕から製造される)物質であり
、動植物体に無害である。Note that this phytic acid is a substance obtained from plant seeds or grains (industrially manufactured from rice cake), and is harmless to animals and plants.
フィチン酸の含有量は、不感脂化処理液における濃度に
おいて、3%以上、好ましくは5%以上である。The content of phytic acid is 3% or more, preferably 5% or more in concentration in the desensitizing treatment liquid.
(b)ここで、スルホサルチル酸としては、5−スルホ
サルチル酸を意味する。4−スルホサルチル酸は訪導体
としてのみ知られているためであるスルホサルチル酸は
水溶液中では酸性を示し、フィチン酸と共存する。しか
し、pHを1.7程度から、これら相互の間で錯体を生
成し初めp)12.0以上になると明らかに錯体の生成
が認められる。又、pHが6.0以上になると該錯体の
構造が変化するこれら錯体の構造は未だ明らかではない
が、モル比法による測定ではr電解移動錯体1であろう
ことが推察できる。なお、錯体の生成はスペクトル吸収
体の赤色移動により明らかである。(b) Here, sulfosalcylic acid means 5-sulfosalcylic acid. This is because 4-sulfosalcylic acid is known only as a conductor.Sulfosalcylic acid exhibits acidity in an aqueous solution and coexists with phytic acid. However, when the pH is raised to about 1.7, complexes begin to form between them, and when the pH reaches 12.0 or higher, the formation of complexes is clearly observed. Further, the structure of these complexes changes when the pH becomes 6.0 or more.Although the structure of these complexes is not yet clear, it can be inferred that it is r-electrotransfer complex 1 by measurement using the molar ratio method. Note that the formation of the complex is evident from the red shift of the spectral absorber.
この錯体水溶液が酸化亜鉛と共存すると、該錯体はスル
ホサルチル酸と亜鉛が交換してフィチン酸と亜鉛は水不
溶性キレートを生成し、再びスルホサルチル酸は水中に
遊離する。このこともスペクトル吸収体の青色移動によ
り明らかである。When this complex aqueous solution coexists with zinc oxide, sulfosalicylic acid and zinc exchange with each other, phytic acid and zinc form a water-insoluble chelate, and sulfosalcylic acid is liberated into water again. This is also evident by the blue shift of the spectral absorber.
前記の特開平1−160691号公報による方法は機能
としては甚だ満足する結果を得られているが前記のよう
な欠点が認められるので実用に供し難い。本発明者はこ
の優れた着想を生かし、さらにこの方法の基本的欠点を
除去しようとする試みである。即ち、キレート交換を意
図する以上、該材料がキレートでなければならない。キ
レートであれば、そのセンターに配位するものは金属で
なければならない。この配位された金属が亜鉛と交換す
るためにはキレート化定数から勘案すると2価以上の金
属イオンでなければならない。本発明者が追試したとこ
ろによると、金属イオンしてクロム(III )が最適
であり、次善がコバルト(III)であることが分った
。基本的問題として金属イオンの存在は不可避であり、
理論的にも前記の欠点は避けられない。本発明者は適当
な有機化合物で、このキレートにかえられないものかと
模索した。もとより金属を含まない有機化合物でキレー
トができる筈がない。従って発想を転換しなければなら
ないことは云うまでもない。Although the method disclosed in Japanese Patent Application Laid-Open No. 1-160691 achieves very satisfactory results in terms of functionality, it is difficult to put it to practical use because of the drawbacks mentioned above. The present inventor has made use of this excellent idea and has also attempted to eliminate the fundamental drawbacks of this method. That is, since chelate exchange is intended, the material must be a chelate. If it is a chelate, the coordination at the center must be a metal. In order for this coordinated metal to exchange with zinc, it must be a divalent or higher metal ion, considering the chelation constant. The inventor conducted further tests and found that chromium (III) is the best metal ion, and cobalt (III) is the second best. The basic problem is that the presence of metal ions is unavoidable.
Theoretically, the above drawbacks are unavoidable. The present inventor sought to find out whether this chelate could be converted into a suitable organic compound. Of course, there is no way that chelates can be formed with organic compounds that do not contain metals. Therefore, it goes without saying that we must change our way of thinking.
(c) フィチン酸とサルチル酸とで水不溶性の白色錯
体沈殿を生成する。しかし、錯体は水に僅かに溶解する
。この反応はサリチル酸特有(サリチル酸は1個のベン
ゼン核に−OHと−COOHを持っている)の反応であ
る様である。ベンゼン核中に−OHがあるだけのフェノ
ールでは錯体は生成せず、又、−COO)!のみを持つ
安息香酸でも錯体は生成されない。(c) Forming a water-insoluble white complex precipitate with phytic acid and salicylic acid. However, the complex is slightly soluble in water. This reaction appears to be unique to salicylic acid (salicylic acid has -OH and -COOH in one benzene nucleus). Phenol that only has -OH in the benzene nucleus does not form a complex, and -COO)! No complex is formed even with benzoic acid, which has only
そこで、フィチン酸−サリチル酸から生成される錯体が
僅かに水に溶解する所に着目し、この同一ベンゼン核に
双極子モーメントの極めて高い基(ラジカル)を導入す
れば、該錯体は水に溶解するであろうと考えた。以上の
思考経路の上に立ってスルホサルチル酸を選出し、実験
の結果考えた様な水可溶性の錯体を得ることができた。Therefore, we focused on the fact that the complex formed from phytic acid-salicylic acid is slightly soluble in water, and if we introduce a group (radical) with an extremely high dipole moment into this same benzene nucleus, the complex will dissolve in water. I thought it would be. Based on the above thought process, we selected sulfosalicylic acid, and as a result of experiments, we were able to obtain a water-soluble complex as we had envisioned.
また、この錯体はフィチン酸/スルホサルチル酸=1/
1及び1/2の錯体ができる。いずれも亜鉛と円滑に交
換してフィチン酸は亜鉛と水不溶性のキレートを生成し
、スルホサルチル酸は遊離する。Also, this complex is phytic acid/sulfosalicylic acid = 1/
1 and 1/2 complexes are formed. Phytic acid exchanges smoothly with zinc to form a water-insoluble chelate with zinc, and sulfosalcylic acid is liberated.
ここで、フィチン酸100部に対するスルホサルチル酸
の配合量は、10〜70部とする(モル比で約0.5前
後から2.0前後)。スルホサルチル酸が10部未満で
は添加効果が非常に弱く、70部を超えても錯体の生成
に寄与せず意味がない。Here, the blending amount of sulfosalcylic acid to 100 parts of phytic acid is 10 to 70 parts (molar ratio of about 0.5 to about 2.0). If the amount of sulfosalcylic acid is less than 10 parts, the effect of addition is very weak, and if it exceeds 70 parts, it does not contribute to the formation of the complex and is meaningless.
なお、不感脂化処理液のpHは、pH:3.0〜6.0
(好ましくはpH:3.8〜5.0)に調整する必要が
ある。不感脂化処理液のpHが上記数値範囲を外れると
、マスターベーパーに地汚れが発生する。In addition, the pH of the desensitization treatment liquid is pH: 3.0 to 6.0.
(preferably pH: 3.8 to 5.0). If the pH of the desensitizing solution is out of the above numerical range, scumming will occur on the master vapor.
上記pH調整剤としてのアルカリは、アルカリ金属イオ
ン(Li、 Na、 K等)、非金属アルカリイオン(
アンモニア;モノエタノールアミン、ジェタノールアミ
ン、トリエタノールアミン等の各種エタノール、アミン
;モノメチルアミン、ジメチルアミン、トリメチルアミ
ン、エチレンジアミン、プロピレンジアミン、フェニレ
ンジアミン等各種アミン類)のいずれを使用してもよい
が、湿し水として不感脂化処理液を薄めて湿し水として
使用する場合は、アルカリ金属塩の方が、印刷中に使用
のインクに異常乳化(いわゆる水まけ)が見られず望ま
しい。なお、上記アルカリは単独でも二種以上を併用し
てもよい。The above-mentioned alkali as a pH adjuster includes alkali metal ions (Li, Na, K, etc.), non-metal alkali ions (
Ammonia; various ethanols such as monoethanolamine, jetanolamine, and triethanolamine; amines; various amines such as monomethylamine, dimethylamine, trimethylamine, ethylenediamine, propylene diamine, and phenylene diamine) may be used; When diluting the desensitizing treatment liquid and using it as a dampening water, an alkali metal salt is preferable because it does not cause abnormal emulsification (so-called watering) in the ink used during printing. In addition, the above-mentioned alkalis may be used alone or in combination of two or more kinds.
(d)なお、本不感脂化処理液の調整に際し、必要に応
じ下記薬剤(d −1)〜(d−7)を添加することが
できる。(d) In addition, when preparing the present desensitizing treatment liquid, the following chemicals (d-1) to (d-7) can be added as necessary.
(d−1)澱粉(可溶性澱粉、デキストリン形を含む)
及びその誘導体、繊維素話導体、ポリアクリル酸ソーダ
、アラビアゴム、プルラン等の一般に使用されている糊
剤。(d-1) Starch (soluble starch, including dextrin type)
and derivatives thereof, fiber conductors, sodium polyacrylate, gum arabic, pullulan, and other commonly used glues.
(d−2)エチレングリコール、プロピレングリコール
、ジエチレングリコール、ポリエチレングリコール、ポ
リプロピレングリコール、グリセリンソルビトール、グ
ルコース、砂糖等のポリオース系の湿潤剤。(d-2) Polyose-based wetting agents such as ethylene glycol, propylene glycol, diethylene glycol, polyethylene glycol, polypropylene glycol, glycerin sorbitol, glucose, and sugar.
(d−3)クエン酸、マロン酸、コハク酸、アジピン酸
、酒石酸、フタール酸等の常識的に使用される有機酸及
びその塩類、安息香酸、ジヒドロ酢酸等の防腐剤。(d-3) Commonly used organic acids such as citric acid, malonic acid, succinic acid, adipic acid, tartaric acid, and phthalic acid, and their salts, and preservatives such as benzoic acid and dihydroacetic acid.
(d−5)ベンゼン、トルエン等の芳香族環にスルホ基
を導入した芳香族スルホン酸及びその塩等の助剤。(d-5) Auxiliary agents such as aromatic sulfonic acids and salts thereof having a sulfo group introduced into the aromatic ring such as benzene and toluene.
(d−6)低級アルコール、エーテル、ケトン、セロソ
ルブ、低級脂肪酸のメチルエステル等の界面張力調整剤
。(d-6) Interfacial tension modifiers such as lower alcohols, ethers, ketones, cellosolves, and methyl esters of lower fatty acids.
(d −7)着色用色素。(d-7) Coloring pigment.
〈発明の効果〉
本発明の不感脂化処理液およびその製造方法は、上記の
如くフィチン酸とスルホサルチル酸を併用することによ
り、フィチン酸−スルホサルチル酸錯体を有効成分とす
るものが得られ、該不感脂化処理液は、後述の実施例で
示す如く、きわめて不感脂化機能が向上し、しかも、二
価以上の金属塩を使用しないため、当該金属イオンの存
在に起因する不具合の発生もない。<Effects of the Invention> The desensitizing treatment liquid of the present invention and the method for producing the same can obtain a product containing a phytic acid-sulfosalcylic acid complex as an active ingredient by using phytic acid and sulfosalcylic acid together as described above. As shown in the examples below, the desensitizing treatment liquid has extremely improved desensitizing function, and since it does not use metal salts of divalent or higher valence, there are no problems caused by the presence of the metal ions. .
本発明の平版印刷用不感脂化処理液は、後述の実施例で
示す如く、充分に実用上耐え得るのみではなく、マスタ
ーペーパーの耐刷可能枚数を大巾に増大できた。即ち、
本発明により、高耐刷に耐え得る新しい実用不感脂化処
理液を提供で幹る。As shown in the examples below, the desensitizing liquid for lithographic printing of the present invention not only has sufficient practical durability, but also greatly increases the number of printable sheets of master paper. That is,
The present invention aims to provide a new practical desensitization treatment solution that can withstand high printing durability.
・〈実施例〉
以下、本発明の効果を確認するために、実施例について
比較例とともに行なった試験例について説明をする。
第1〜2表にそれぞれ示す処方の水溶液を、表示の各ア
ルカリを使用してp)I:4.2〜4.3に調整し、各
実施例・比較例の不感脂化処理液を調製した。・<Example> Hereinafter, in order to confirm the effects of the present invention, test examples that were conducted along with comparative examples will be explained.
Aqueous solutions of the formulations shown in Tables 1 and 2 were adjusted to p)I: 4.2 to 4.3 using the indicated alkalis to prepare desensitizing treatment solutions for each example and comparative example. did.
各不感脂化処理液を製版されたマスターペーパー塗布す
るとともに、20倍に水で希釈したものを湿し木とした
。Each desensitization treatment solution was applied to a master paper made of a plate, and the solution was diluted 20 times with water to make a damp wood.
そして、通常のオフセット印刷機を使用して印刷インク
(マスターブルー:■日研化学研究所製商品名)で中性
紙に印刷をした。Then, printing was performed on neutral paper using a printing ink (Master Blue: ■trade name manufactured by Nikken Kagaku Kenkyusho) using a normal offset printing machine.
マスターペーパー(耐刷枚数=3千枚保証)1枚につき
5千枚のオフセット印刷を行った。各実施例の処理液の
場合は、いずれも5千枚まで、マスターベーパーに地汚
れその他の異常は何ら認められず良好な印刷物が得られ
た。他方、各比較例の処理液を使用した場合は、いずれ
も、刷り出しよりマスターペーパー及び印刷用紙の非画
線部にの地汚れが発生し、実用に耐えなかった。5,000 sheets of offset printing was performed for each sheet of master paper (guaranteed print life = 3,000 sheets). In the case of the treatment liquid of each example, good printed matter was obtained without any scumming or other abnormalities on the master vapor up to 5,000 sheets. On the other hand, when the processing liquids of each comparative example were used, scumming occurred in the non-printing areas of the master paper and printing paper from the beginning of printing, and they were not suitable for practical use.
なお、各実施例における刷り終り後の各マスターベーパ
ーを、さらに詳細に調べた所、画線部のトナーに対する
影響が異常に小さかった。この現象は水溶液中にはフリ
ーのフィチン酸は存在せず、総てスルホサルチル酸と錯
体を造ってガードされているためトナー(樹脂:有機高
分子)への化学的なインパクトが著しく弱化されている
ためと推定される。Further detailed examination of each master vapor after printing in each example revealed that the influence on the toner in the image area was abnormally small. This phenomenon occurs because there is no free phytic acid in the aqueous solution, and all of it is protected by forming a complex with sulfosalcylic acid, so the chemical impact on the toner (resin: organic polymer) is significantly weakened. It is estimated that this is due to
上記各実施例において、5千枚印刷後、さらに、印刷を
m続したが、トータル1万枚刷っても印刷紙に印刷汚れ
は発生せず印刷可能であった。In each of the above examples, after printing 5,000 sheets, printing was continued for an additional m, but even after printing a total of 10,000 sheets, printing was possible with no printing stains occurring on the printing paper.
さらに、湿し木の特性は、極性溶剤を添加したものの方
(実施例17・18)が優れていた。また、pH8製剤
として有機アルカリを使用した不感脂化処理液を薄めて
湿し水に使用した実施例6〜12は、印刷中に使用イン
クにやや異常乳化がみられたが、印刷物には、何ら影響
はなかった。Furthermore, the properties of damp wood were better in those to which a polar solvent was added (Examples 17 and 18). In addition, in Examples 6 to 12, in which a desensitizing solution using an organic alkali as a pH 8 formulation was diluted and used as a dampening solution, some abnormal emulsification was observed in the ink used during printing, but the printed matter was There was no effect.
電 1 夷 (JL位二部) 箪 2 男 (−11位・部)Den 〷 (JL rank 2nd division) Chest 2 Male (-11th place/division)
Claims (1)
不感脂化処理液において フィチン酸100重量部に対してスルホサルチル酸10
〜70重量部が配合された組成物の水溶液を主体とし、
pH:3.0〜5.0に調製されてなることを特徴とす
る平版印刷版の不感脂化処理液。 2、キレート剤としてフィチン酸を用いる平版印刷版の
不感脂化処理液の製造方法において、水溶液中でフィチ
ン酸とスルホサルチル酸とからなる錯体を生成させ、p
H:3.0〜5.0に調製して製造することを特徴とす
る平版印刷版の不感脂化処理液の製造方法。[Claims] 1. In a desensitizing treatment solution for lithographic printing plates using phytic acid as a chelating agent, 10 parts by weight of sulfosalicylic acid is added to 100 parts by weight of phytic acid.
The main component is an aqueous solution of a composition containing ~70 parts by weight,
A desensitizing treatment liquid for lithographic printing plates, which is adjusted to have a pH of 3.0 to 5.0. 2. In a method for producing a desensitizing solution for lithographic printing plates using phytic acid as a chelating agent, a complex consisting of phytic acid and sulfosalicylic acid is generated in an aqueous solution, and p
A method for producing a desensitizing treatment liquid for a lithographic printing plate, characterized in that the desensitization treatment liquid for a lithographic printing plate is produced by adjusting H: 3.0 to 5.0.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10701990A JP2744986B2 (en) | 1990-04-23 | 1990-04-23 | Desensitizing solution for lithographic printing plate and method for producing the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10701990A JP2744986B2 (en) | 1990-04-23 | 1990-04-23 | Desensitizing solution for lithographic printing plate and method for producing the same |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH045089A true JPH045089A (en) | 1992-01-09 |
JP2744986B2 JP2744986B2 (en) | 1998-04-28 |
Family
ID=14448453
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10701990A Expired - Fee Related JP2744986B2 (en) | 1990-04-23 | 1990-04-23 | Desensitizing solution for lithographic printing plate and method for producing the same |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2744986B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62137530A (en) * | 1985-12-11 | 1987-06-20 | Toa Harbor Works Co Ltd | Method and apparatus for measuring friction force on circumferential surface of pile |
-
1990
- 1990-04-23 JP JP10701990A patent/JP2744986B2/en not_active Expired - Fee Related
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62137530A (en) * | 1985-12-11 | 1987-06-20 | Toa Harbor Works Co Ltd | Method and apparatus for measuring friction force on circumferential surface of pile |
Also Published As
Publication number | Publication date |
---|---|
JP2744986B2 (en) | 1998-04-28 |
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