JPH01108280A - Drying agent for lithographic ink - Google Patents
Drying agent for lithographic inkInfo
- Publication number
- JPH01108280A JPH01108280A JP62267462A JP26746287A JPH01108280A JP H01108280 A JPH01108280 A JP H01108280A JP 62267462 A JP62267462 A JP 62267462A JP 26746287 A JP26746287 A JP 26746287A JP H01108280 A JPH01108280 A JP H01108280A
- Authority
- JP
- Japan
- Prior art keywords
- drying
- ink
- water
- drying agent
- lithographic ink
- 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
- 239000002274 desiccant Substances 0.000 title claims abstract description 22
- 150000004972 metal peroxides Chemical class 0.000 claims abstract description 8
- 238000001035 drying Methods 0.000 abstract description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 12
- -1 CaO2 Chemical class 0.000 abstract description 2
- 235000019402 calcium peroxide Nutrition 0.000 abstract description 2
- 239000000470 constituent Substances 0.000 abstract 2
- 239000000976 ink Substances 0.000 description 26
- 239000007800 oxidant agent Substances 0.000 description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- ZJRXSAYFZMGQFP-UHFFFAOYSA-N barium peroxide Chemical compound [Ba+2].[O-][O-] ZJRXSAYFZMGQFP-UHFFFAOYSA-N 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000001934 delay Effects 0.000 description 2
- 230000003111 delayed effect Effects 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 description 2
- 239000008158 vegetable oil Substances 0.000 description 2
- 239000004343 Calcium peroxide Substances 0.000 description 1
- SPAGIJMPHSUYSE-UHFFFAOYSA-N Magnesium peroxide Chemical compound [Mg+2].[O-][O-] SPAGIJMPHSUYSE-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- NIPNSKYNPDTRPC-UHFFFAOYSA-N N-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 NIPNSKYNPDTRPC-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- LHJQIRIGXXHNLA-UHFFFAOYSA-N calcium peroxide Chemical compound [Ca+2].[O-][O-] LHJQIRIGXXHNLA-UHFFFAOYSA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- 229960004995 magnesium peroxide Drugs 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000010893 paper waste Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 230000002747 voluntary effect Effects 0.000 description 1
Landscapes
- Inks, Pencil-Leads, Or Crayons (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は平版印刷インキ用乾燥剤に関し、更に詳しくは
、平版印刷インキに混入することによって、湿し水によ
る高湿度下に於いて該インキを乾燥させるために使用す
る乾燥剤に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a desiccant for lithographic printing ink, and more specifically, by mixing it into lithographic printing ink, the drying agent can be used to dry the ink under high humidity caused by dampening water. It relates to a desiccant used for drying.
乾燥性植物油の酸化重合によって乾燥する平版油性イン
キの乾燥剤は鉛、マンガン及びコバルトの脂肪酸塩又は
、硼酸塩が従来から使用されている。これらの中コバル
トは主にインキ皮膜の表面乾燥、鉛は底部の乾燥、そし
てマンガンは中間層の乾燥を一般的につかさどり、これ
らの混用によってバランスのとれたインキ皮膜の乾燥触
媒として働くことは事実である。しかし乍ら、平版印刷
は湿し水を使用するため被印刷物の表面又は内層に水分
が残留し、たとえ従来各種乾燥剤を使用したとしても、
この水分がインキの乾燥速度を著しく低下させ、印刷物
の品質劣化や納期遅延と言ったトラブルを頻繁に誘発し
ているのが現状である。Fatty acid salts of lead, manganese, and cobalt or borates have conventionally been used as desiccants for lithographic oil-based inks that are dried by oxidative polymerization of drying vegetable oils. Among these, cobalt is mainly responsible for drying the surface of the ink film, lead is responsible for drying the bottom layer, and manganese is generally responsible for drying the intermediate layer, and it is true that the combination of these works as a catalyst for drying a well-balanced ink film. It is. However, since lithographic printing uses dampening water, moisture remains on the surface or inner layer of the printing material, and even if various drying agents have been used in the past,
The current situation is that this moisture significantly reduces the drying speed of ink, frequently causing problems such as deterioration in the quality of printed matter and delays in delivery.
本発明者はこう言ったインキの乾燥遅延に伴って起きる
品質劣化、例えばチョーキング、光沢不良、耐摩擦不良
等や納期遅延を完全に解消するために、被印刷体に湿し
水が残留し高湿度の状態においても充分に乾燥が可能な
乾燥剤を開発するために研究を続けた結果、本発明を完
成した。In order to completely eliminate the quality deterioration that occurs due to delayed drying of ink, such as chalking, poor gloss, poor friction resistance, etc., as well as delivery delays, we have developed As a result of continuing research to develop a desiccant that can sufficiently dry even in humid conditions, the present invention was completed.
この問題点は、平版印刷インキ用乾燥剤として水不溶性
の金属過酸化物を使用することにより解決される。This problem is solved by using water-insoluble metal peroxides as drying agents for lithographic printing inks.
本発明者は水と接触することによって酸素と酸化剤を放
出する化合物すなわち不溶性金属の過酸化物を平版印刷
用油性インキ中に混入する事により放出する酸素と酸化
剤の作用により著しくインキ乾燥速度を早めうろことを
見出したものである、特に大きな特徴は水が存在するこ
とにより、更に乾燥が一段と促進されることである。The present inventor has discovered that by mixing a compound that releases oxygen and an oxidizing agent upon contact with water, that is, an insoluble metal peroxide, into an oil-based ink for lithographic printing, the ink drying rate is significantly increased due to the action of the released oxygen and oxidizing agent. A particularly significant feature of this study is that the presence of water further accelerates drying.
本発明に於いて使用する金属過酸化物としては水不溶性
のものであれば広く使用出来、その代表例としては過酸
化バリウム、過酸化マグネシウム、過酸化カルシウム等
であるが、本発明ではこれらの金属に限定されるもので
はない。The metal peroxide used in the present invention can be widely used as long as it is water-insoluble, and typical examples include barium peroxide, magnesium peroxide, calcium peroxide, etc. It is not limited to metal.
これらの金属過酸化物が水の存在下すなわち平版印刷に
おける湿し水を包含した状態に於いて生ずる酸素、酸化
剤の生成機構は次のような反応式%式%
尤もこれらの金属過酸化物はそれ自体でも酸化剤として
の作用を有するが、かなり安定な化合物であるため加熱
しなければ酸化剤として働きにくい傾向があり、水によ
って過酸化水素を生成させてこの生成物を酸化剤として
作用させる方が効果が大きい。The formation mechanism of oxygen and oxidizing agents that occur in the presence of water, that is, when these metal peroxides contain dampening water in lithographic printing, is expressed by the following reaction formula. itself acts as an oxidizing agent, but since it is a fairly stable compound, it tends not to act as an oxidizing agent unless heated. Hydrogen peroxide is generated with water and this product acts as an oxidizing agent. It is more effective to do so.
本発明はこのように平版印刷用油性インキの主成分であ
る乾燥性植物油を該金属過酸化物から水の作用によって
生ずる酸化剤としてのH,Otとフリーの02ガスの相
乗効果によって酸化重合による乾燥を行わせるのに著し
く効果的である。In this way, the present invention uses drying vegetable oil, which is the main component of oil-based ink for lithographic printing, through oxidative polymerization using the synergistic effect of H, Ot as oxidizing agents generated by the action of water from the metal peroxide, and free 02 gas. It is extremely effective in drying.
本発明の乾燥剤は通常平版印刷インキ100重量部に対
し、1〜10重景部、好ましくは2〜6重量部程度配合
される。The drying agent of the present invention is usually blended in an amount of about 1 to 10 parts by weight, preferably about 2 to 6 parts by weight, per 100 parts by weight of the lithographic printing ink.
本発明の乾燥剤の使用方法は従来のこの種乾燥剤と同じ
であり、予めインキ調整時に配合しても良く、また印刷
時にインキに配合してもよい。The method of using the desiccant of the present invention is the same as that of conventional desiccants of this kind, and it may be blended in advance when preparing the ink, or may be blended into the ink during printing.
また本発明の乾燥剤はこれ単独でも使用出来るばかりで
なく、従来の乾燥剤と併用して使用することも出来る。Furthermore, the desiccant of the present invention can not only be used alone, but also in combination with conventional desiccants.
〈実施例〉
実施例1−3
平版印刷インキrNo、2合成紙用超耐光紅」(東華色
素化学工業畑製)100重量部に、第1表に示す乾燥剤
を所定の割合で配合し均一に混練した。<Example> Example 1-3 100 parts by weight of lithographic printing ink rNo. 2 Super light-fast red for synthetic paper (manufactured by Toka Shiki Kagaku Kogyo Hata) was mixed with the desiccant shown in Table 1 in a predetermined ratio and uniformly mixed. It was kneaded.
比較例1
実施例1と同じインキに第1表に示す訂正の乾燥剤を所
定量配合し充分混練した。Comparative Example 1 A predetermined amount of the corrected drying agent shown in Table 1 was added to the same ink as in Example 1 and thoroughly kneaded.
但し第1表中のrUGドライヤー」とは従来から使用さ
れている乾燥剤で合同インキ■製のものである。またC
a0z ’N025J 、Bang及びMg0z ’
NO2O」はいずれも冨田製薬■製のものである。However, "rUG dryer" in Table 1 is a conventionally used drying agent manufactured by Godo Ink (■). Also C
a0z 'N025J, Bang and Mg0z'
NO2O'' are all manufactured by Tomita Pharmaceutical ■.
く試験−1〉
上記の各インキを夫々R1テスター(明製作所製)なる
展色機にてインキ膜厚2μで上質紙及び合成紙「ユボ」
(玉子油化社製)へ展色した。それぞれの展色見本を
夫々直ちに半分に切断し、−方をオーブンの乾燥無水状
態で、他の一方を充分に含水させた状態で夫々ポリ袋に
挿入密閉し、その乾燥時間の測定を行った。雰囲気温度
はいずれも常温(22°C)である。これらの結果を第
2表に示す。Test-1> Each of the above inks was applied to high-quality paper and synthetic paper "Yubo" with an ink film thickness of 2μ using a color spreader called R1 Tester (manufactured by Mei Seisakusho).
(manufactured by Tamago Yuka Co., Ltd.). Each developed color sample was immediately cut in half, one half was dried in an oven in an anhydrous state, the other half was fully hydrated, and each was inserted into a plastic bag and sealed, and the drying time was measured. . The ambient temperature in all cases was room temperature (22°C). These results are shown in Table 2.
第1表
第2表
上記第2表から明らかな通り従来のドライヤーのみを用
いた比較例1は含水状態で著しく乾燥が遅れるのに対し
本発明における実施例1〜3は含水状態で著しく乾燥速
度が促進される。特に過酸化バリウムを用いた実施例2
はインキの乾燥速度が極めて早い。Table 1 Table 2 As is clear from Table 2 above, in Comparative Example 1 using only the conventional dryer, the drying time was significantly delayed in the water-containing state, whereas in Examples 1 to 3 of the present invention, the drying speed was remarkable in the water-containing state. is promoted. Example 2, especially using barium peroxide
The drying speed of the ink is extremely fast.
く試験−2〉
試験−1に示した乾燥はすべてインキ皮膜の粘着性(ア
フタータック)が完全に消滅した完全乾燥のデーターで
ある。印刷直後における被印刷物を棒積する際に生じる
裏移りのトラブルは、印刷インキの指接触乾燥(セット
)によって支配される。試験−1と同様に展色した直後
の各インキについて、上質紙展色面に白い上質紙を重ね
たもの、合成紙屑色面に白い合成紙を重ねたものの夫々
についてその上からR1テスターにて硬度70度、直径
65mのゴムロールを10分きざみで断続的にころがし
、時々水を補給し紙を湿らせ乍ら白紙への裏移り状態を
観察した。加えた圧力は線圧12閾巾である。裏移りし
なくなった時点を指触乾燥の終点としその結果を第3表
に示す。Test-2> All the drying data shown in Test-1 is complete drying data in which the tackiness (aftertack) of the ink film has completely disappeared. The problem of set-off that occurs when printing substrates are piled up immediately after printing is dominated by finger contact drying (setting) of the printing ink. For each ink immediately after color spreading in the same way as in Test-1, use the R1 tester to apply the results to the surface of high-quality paper with white high-quality paper overlaid on the colored side, and the white synthetic paper overlaid on the colored side of synthetic paper waste using the R1 tester. A rubber roll with a hardness of 70 degrees and a diameter of 65 m was rolled intermittently in 10 minute increments, and while water was occasionally added to moisten the paper, the state of set-off onto the white paper was observed. The applied pressure is a linear pressure of 12 thresholds. The end point of dryness to the touch was defined as the point at which no set-off occurred, and the results are shown in Table 3.
第3表
〈発明の効果〉
本発明で用いる過酸化物は従来のドライヤーに比ベイン
キ乾燥の能率を一段と向上させインキの乾燥遅延によっ
て生じる印刷中のトラブル(印刷適性)及び印刷後のト
ラブル(印刷物適性)をすべて解消させるに効果著しい
ものである。Table 3 <Effects of the Invention> The peroxide used in the present invention further improves the efficiency of ink drying compared to conventional dryers. It is extremely effective in eliminating all problems (aptitude).
(以上)
特許出願人 キングプリンティング株式会社手続補正
書(自発)
1、!IC件の表示
昭和62年 特 許 願 第267462号2、発明の
名称
平版印刷インキ用乾燥剤
3、補正をする者
事件との関係 特許出願人住所
大阪市西成区玉出西2丁目7番16号氏名 キングプ
リンティング株式会社取締役社長 津 村 卓
4、代理人
〒530 大阪市北区南森町1の1の25八千代ビル
南館 !06 (314) 0248番明細書の発明の
詳細な説明の項
6、補正の内容
別紙の通り補正する。(Above) Patent applicant King Printing Co., Ltd. Procedural amendment (voluntary) 1.! Indication of IC case 1988 Patent Application No. 267462 2 Name of the invention Desiccant for lithographic printing ink 3 Relationship with the person making the amendment Patent applicant address
2-7-16 Tamade Nishi, Nishinari-ku, Osaka Name: King Printing Co., Ltd. President Taku Tsumura 4, Agent: 25 Yachiyo Building South Building, 1-1 Minamimorimachi, Kita-ku, Osaka 530! 06 (314) Item 6 of the Detailed Description of the Invention in Specification No. 0248, Contents of the Amendment The amendment is made as shown in the attached sheet.
補正の内容
(1)明細書5頁5行中「訂正」を「所定」と補正する
。Contents of amendment (1) "Correction" in line 5 on page 5 of the specification is amended to read "prescribed."
以上that's all
Claims (1)
インキ用乾燥剤Desiccant for lithographic printing ink containing water-insoluble metal peroxide as main component
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62267462A JPH01108280A (en) | 1987-10-21 | 1987-10-21 | Drying agent for lithographic ink |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62267462A JPH01108280A (en) | 1987-10-21 | 1987-10-21 | Drying agent for lithographic ink |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01108280A true JPH01108280A (en) | 1989-04-25 |
JPH0257101B2 JPH0257101B2 (en) | 1990-12-04 |
Family
ID=17445173
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62267462A Granted JPH01108280A (en) | 1987-10-21 | 1987-10-21 | Drying agent for lithographic ink |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01108280A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0346487U (en) * | 1989-09-18 | 1991-04-30 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS51132236A (en) * | 1974-12-28 | 1976-11-17 | Matsushita Electric Works Ltd | After-treatment method of a coating of inorganic paints |
JPS582367A (en) * | 1981-06-29 | 1983-01-07 | Adogaa Kogyo Kk | Ink composition |
-
1987
- 1987-10-21 JP JP62267462A patent/JPH01108280A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS51132236A (en) * | 1974-12-28 | 1976-11-17 | Matsushita Electric Works Ltd | After-treatment method of a coating of inorganic paints |
JPS582367A (en) * | 1981-06-29 | 1983-01-07 | Adogaa Kogyo Kk | Ink composition |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0346487U (en) * | 1989-09-18 | 1991-04-30 | ||
JPH0547170Y2 (en) * | 1989-09-18 | 1993-12-10 |
Also Published As
Publication number | Publication date |
---|---|
JPH0257101B2 (en) | 1990-12-04 |
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