JPS59159863A - Composition for printing ink - Google Patents
Composition for printing inkInfo
- Publication number
- JPS59159863A JPS59159863A JP58034209A JP3420983A JPS59159863A JP S59159863 A JPS59159863 A JP S59159863A JP 58034209 A JP58034209 A JP 58034209A JP 3420983 A JP3420983 A JP 3420983A JP S59159863 A JPS59159863 A JP S59159863A
- Authority
- JP
- Japan
- Prior art keywords
- composition
- modified
- ink
- printing
- printing 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
Abstract
Description
【発明の詳細な説明】
本発明は印刷インク用組成物に関し、四に詳しくはオフ
セント印刷インク用組成物に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a composition for printing ink, and more particularly to a composition for offset printing ink.
オフセット印刷は、金属や樹脂などの原版に店内したイ
ンクを直接紙に移さず、一度ゴムの而(ゴムのブランケ
ットが印刷機のゴム胴に巻付けである。)に移し、これ
から紙に再転写する印刷方法で、硬い金属版面などから
じかに印刷する方法と比べて、ゴムの弾性゛を利用して
インクを移すことが出来る為、紙の表面が粗い場合でも
少ない印圧で印刷でき、美麗な印刷効果が得られるのが
特徴である。In offset printing, the ink that is placed on an original plate made of metal or resin is not transferred directly to the paper, but is first transferred to a rubber blanket (a rubber blanket is wrapped around the rubber cylinder of the printing machine), and then retransferred onto the paper. This is a printing method that uses the elasticity of rubber to transfer ink, compared to methods that print directly from a hard metal plate, so even if the surface of the paper is rough, it can be printed with less printing pressure, resulting in beautiful results. Its feature is that it produces a printing effect.
しかし、オフセット印刷は、上記のごとくゴムのブラン
ケットを介してインクを再転写することからインク皮膜
が薄い欠点を有しており、この欠点を補うためインク組
成物には着色力の大きい色料が多量に配合されている。However, as mentioned above, offset printing has the disadvantage that the ink film is thin because the ink is retransferred through a rubber blanket, and to compensate for this disadvantage, the ink composition contains a colorant with high tinting power. Contains a large amount.
その結果印刷後印刷物を重ねて訃〈と着色力の大きい色
料による裟うつりが起りやすく、この裏うつりの防止が
オフセット印刷における課題の一つとなっている。As a result, when printed materials are stacked after printing, smearing due to colorants with high coloring power is likely to occur, and prevention of this smearing is one of the challenges in offset printing.
そこで種々の裏うつ9防止策が検討され、例えばインク
組成物に低分子量ポリテトラフlレオロエチレン(以下
低分子量PTFEという。)粉衣を少量添加しよく分散
させておくと効果のあることが見い出された。しかし、
低分子量PTFE粉木を粉衣したインク組成物は、該低
分平置PTF Eの分散性および分散安定性が悪くイン
ク溜め中でra Uk分子)、にP T F Eの凝集
および沈降が起シやすく所期の目的を充分に達し得なか
った。Therefore, various preventive measures have been investigated, and it has been found that it is effective to add a small amount of low molecular weight polytetrafluoroethylene (hereinafter referred to as low molecular weight PTFE) powder to the ink composition and disperse it well. . but,
Ink compositions coated with low-molecular-weight PTFE powder have poor dispersibility and dispersion stability of the low-molecular-weight PTFE, which causes aggregation and sedimentation of the PTFE in the ink reservoir (raUk molecules). However, the intended purpose could not be fully achieved.
そこで本発明者らはさらに分散性および分散安定14:
の良好な添加剤を鋭怠研究した結果、特定の低分子量フ
ッ素樹脂系共重合体が少量で裏 ゛うつり防止に効果が
あり、かつ分散性および分散安定性が良好であることを
見い出し本発明を完成するに到った。Therefore, the present inventors further investigated dispersibility and dispersion stability14:
As a result of extensive research into good additives, it was discovered that a small amount of a specific low molecular weight fluororesin copolymer is effective in preventing backing, and has good dispersibility and dispersion stability, and the present invention has been made. I have come to complete this.
すなわち本究明は、ビヒクルに変性低分子量ポリテトラ
フルオロエチレンを混合分散してなる印刷インク用組成
物を髪旨とするものである。That is, the present study aims to provide a printing ink composition comprising a modified low molecular weight polytetrafluoroethylene mixed and dispersed in a vehicle.
本発明で用いられるビヒクルは、印刷1に用いられるビ
ヒクルで、例えばロジン変性フェノール6?J IIR
、Mフェノールる’j脂、ロジンエステ7し、ロンン変
性マレイン酸樹脂、石灰化ロジン、スチレン化アIレキ
ド樹脂、ロジン変性ツマlし酸樹廂、脂肪酸変性アルキ
ド樹脂、ポリアミド樹脂、キシレン掴11旨等でそれぞ
れ単独または2神以上混合して用いられる。The vehicle used in the present invention is the vehicle used in printing 1, such as rosin-modified phenol 6? JIIR
, M phenol resin, rosin ester resin, Ronne modified maleic acid resin, mineralized rosin, styrenated resin, rosin modified resin, fatty acid modified alkyd resin, polyamide resin, xylene grip 11 effect They are used alone or in combination of two or more.
本発明で用いられる変性低分子も目ζリテトラフルオロ
エチレントハ、テ1−ラフル刃−ロエfし760〜99
.999−r= tし%ト含フッ9gU−A’Vフィン
0.001〜40モル%との共重合体のことをいい、共
重合(で供せられる含フツ素α−オレフィンは、一般式
:
%式%
(式中、Rは塩素または炭素数1〜IOの/く−フルオ
ロまたはポリフルオロアルキ7し基または炭とがめる。The modified low molecules used in the present invention are
.. 999-r= refers to a copolymer with 0.001 to 40 mol% of fluorine-containing 9g U-A'V fins, and the fluorine-containing α-olefin provided by copolymerization is expressed by the general formula : % formula % (wherein R is chlorine, a C-fluoro or polyfluoroalkyl group having 1 to 10 carbon atoms, or carbon.
)
で表わされる化合物で、前記ビヒクル100重量部に対
し20重11に部以下の割合で添加混合して用いられる
。), which is used by adding and mixing at a ratio of 20 parts by weight or less to 11 parts by weight per 100 parts by weight of the vehicle.
この父性低分子11トポリテトラフルオロエチレンは、
連鎖移動剤を用いて重合するかあるいは高分子策の女性
テトラフルオロエチレンを″電子線、熱等で分解するこ
とによってΦジ造でき、通常れl径は0.1〜50 p
m数平均分子8+1は1,000〜50.0(10で
ある。この含フツ素α−オレフィンの共重合比は、−1
= 、(c!範囲が好ましく上記範囲より小であると分
散性および分散安定性が悪く、上記範囲より大であると
非粘着性が低下し裏うつりが起りやすい。This paternal low molecular weight 11-topolytetrafluoroethylene is
It can be formed by polymerization using a chain transfer agent or by decomposing a polymeric female tetrafluoroethylene using an electron beam, heat, etc., and the diameter is usually 0.1 to 50 p.
The m number average molecule 8+1 is 1,000 to 50.0 (10. The copolymerization ratio of this fluorine-containing α-olefin is -1
=, (c! range is preferred. If it is smaller than the above range, the dispersibility and dispersion stability will be poor, and if it is larger than the above range, the non-adhesive property will be decreased and backing will easily occur.
本発明の印刷インクflJ組我物は、前記のと卦すヒヒ
クルおよび変性低分子↑j)ポリテトラフルオロエチレ
ンとか−らなっているが、この組成物にさらに常法に従
い色料、溶剤およびその他補助剤や必要に応じ他のフッ
素系添加剤を加えることによりオフセット印刷用インク
となすことができる。壕だ所望により1i11常の組成
変四で他の印刷用(例えば凸版または凹版)インクとし
て用いることもできる。The printing ink flJ composition of the present invention consists of the above-mentioned vehicle and modified low molecular weight ↑j) polytetrafluoroethylene, but this composition is further supplemented with colorants, solvents and other substances according to a conventional method. By adding auxiliary agents and other fluorine-based additives as necessary, it can be made into an ink for offset printing. It can also be used as an ink for other printing applications (for example letterpress or intaglio) with different compositions if desired.
次に実施例、比較例および参考例を示し本発明を具体的
に説明する。Next, the present invention will be specifically explained with reference to Examples, Comparative Examples, and Reference Examples.
′*施何例
ポリアミド樹脂(粘度100CP、比重0.9.25°
C)959 (fc変性低分子fj%ポリテトラフルオ
ロエチレン(テトラフルオロエチレン99.78モアし
%おヨヒヘキサフル万ロプロピレン0.22モ/I/%
の共重合体、数平均分子量5,000〜10,000
、粒径02〜0゜4μm)5yを添加しターボ型分散機
を用いよく混合した。この混合物を試料として次に示す
引きFM発生深さく分散性)および沈降度(分散安定性
)の測定を行った。'*Example polyamide resin (viscosity 100CP, specific gravity 0.9.25°
C) 959 (fc modified low molecular weight fj% polytetrafluoroethylene (tetrafluoroethylene 99.78 mole%, hexafluoropropylene 0.22 mole/I/%
copolymer, number average molecular weight 5,000 to 10,000
, particle size 02-0°4 μm) was added and mixed well using a turbo disperser. This mixture was used as a sample to measure the following FM generation depth (dispersibility) and sedimentation degree (dispersion stability).
引き跡発生深さく分散性)(、IIS K 510
1 Kンドメーターのみその一番深いところへ、みぞ全
体を名;奇たす漬より幾分多く流し込みスクレーパーの
上部の両端に近いところを持ち、みそを旧;角に(工1
7切るようにしてみその深い方の末端に刃をあて、一定
の速度でみその浅い方へ引いた。引き終わってから10
秒以内に拡散照光の−Fで、グラインドメーターの短辺
に対し111角の方向の真北から引き跡を見、3本以上
の線が出始めたところの目盛(引き跡発生深さ、1im
)を記録した。この操作を5回繰り返して、その平均値
を求めた。Trace generation depth and dispersion) (, IIS K 510
1. Pour the entire groove into the deepest part of the kettle, holding the top of the scraper near both ends, and pour the miso into the corner (1st step).
Place the blade at the deep end of the miso in a 7-slice motion, and pull it toward the shallow end of the miso at a constant speed. 10 after drawing
Within seconds, with -F of the diffused illumination, look at the trace from due north in the direction of 111 angle to the short side of the grindmeter, and mark the scale where three or more lines start to appear (depth of trace occurrence, 1 inch).
) was recorded. This operation was repeated five times and the average value was determined.
この引@跡発生深さくμm)の(Ii“「が小さいほど
分散性が良好(すなわち添加剤が4−集していない。)
なととを示す。The smaller the (Ii") of this trace (depth of trace occurrence μm), the better the dispersibility (i.e., the additive is not aggregated).
Indicates natoto.
な、(、−、クラインドメーターとけ〆11に示すよう
なもので、長さ200〜250 mm 、幅100〜1
50mm。(,-, Kleindometer Tokeshiki 11), length 200-250 mm, width 100-1
50mm.
厚さ15〜254mの硬質特殊合金でflEられ、その
平滑な一面に、長さ120〜160 mm、幅15〜2
5mm。It is made of a hard special alloy with a thickness of 15 to 254 m, and on one smooth surface there are 120 to 160 mm in length and 15 to 2 mm in width.
5mm.
深さ25μm若しくは125μmから0捷で連続的に傾
斜した、極めて薄いくさび形をし/(みぞが1本又は2
本ある。みその横の目盛はその位置での深さで、マイク
ロメ−)1しく tt 乳)で表されている。It has an extremely thin wedge shape that is continuously sloped from a depth of 25 μm or 125 μm (with one or two grooves).
There are books. The scale next to the miso is the depth at that position, expressed in micrometres.
スクレーバーとは図2に示すようなもので、長さ90〜
100 mm、幅40〜60mm、Juさ5〜10 m
m 、クラインドメーターと同質の合金からなり、刃先
は正確に一直線をなしているが、刃グCは琵25μmの
丸み帯びている。The scraper is as shown in Figure 2, and has a length of 90~
100 mm, width 40-60 mm, height 5-10 m
It is made of the same alloy as the Klein meter, and the cutting edge is exactly in a straight line, but the cutting edge C is rounded to a diameter of 25 μm.
測定結果を表1に示す。The measurement results are shown in Table 1.
沈降度(分散安定性)
mI記混合物のうち25+++tを混合後ただちに14
II・mlX 16Q +nmの試1験$■にとり密閉
し25”Cで72時間直立静置し添加剤の沈降度し)を
測定した。Sedimentation degree (dispersion stability) Immediately after mixing 25+++t of the mI mixture, 14
II・mlX 16Q +nm test 1 test $■ The sample was sealed and allowed to stand upright at 25"C for 72 hours, and the degree of sedimentation of the additive was measured.
ここでいう沈降度(イ)とは、前記試験管の底面から液
面せでの長さく4)で、該液面から沈降した添加剤の上
部までの長さ(B)を除した値に100を乗じた値をい
い、数式:
%式%
で表わされ、沈降度(%)の小さな値はど添加剤が沈降
、分離しに〈〈分散安定性が良好なことを示す。The degree of sedimentation (A) here is the value obtained by dividing the length from the bottom of the test tube to the liquid surface (4) by the length (B) from the liquid surface to the top of the sedimented additive. It refers to the value multiplied by 100 and is expressed by the formula: %. A small value of the degree of sedimentation (%) indicates that the additive has good dispersion stability due to sedimentation and separation.
」1定結果をねI[記引き跡発生深さくμm)とともに
表1に示1寸。The results are shown in Table 1 along with the depth of occurrence of scratches in μm.
実施例2〜4
表1に示す変性低分子量ポリテトラフルオロエチレンを
用い、他は実施例1と同様の操作で混合争および測定を
行った。Examples 2 to 4 Using the modified low molecular weight polytetrafluoroethylene shown in Table 1, mixing and measurements were carried out in the same manner as in Example 1 except for the following.
測定結果を表1に示す。The measurement results are shown in Table 1.
比較例1〜2
表1に示す低分子量ポリテトラフルオロエチレンを変t
t低分平置ポリテトラフ7レオロエチレンの代りに用い
、他は実施例1と同様の操作で混合および測定を行った
。Comparative Examples 1 to 2 The low molecular weight polytetrafluoroethylene shown in Table 1 was modified to
Mixing and measurement were carried out in the same manner as in Example 1, except that low-minute flat polytetraph 7 was used in place of rheoloethylene.
測定結果を実施例1〜4と共に表1に示す。The measurement results are shown in Table 1 together with Examples 1 to 4.
参考例
比較例1および実施例1で調製したそれぞれの印刷イン
ク用組成物40重量部にシアニングルー20重量部、ビ
クトリアブルーレーキ9重量部、グロスホワイト20重
量部、シリコンフェス10重量部およびホウ酸鉛0.5
重量部を加えロールミルを用い90°Cで2時間混練し
印刷インクとなした。比較例1の組成物から調製したイ
ンクのフロー値は18、タンク値は9.0、臨界表面張
力は20ダイン/釧で、実施例1の組成物から調製した
インクのフロー値は18、タック値は9.5、臨界表面
張力は21ダイン/anであった。Reference Example 40 parts by weight of each printing ink composition prepared in Comparative Example 1 and Example 1, 20 parts by weight of cyanine blue, 9 parts by weight of Victoria Blue Lake, 20 parts by weight of Gloss White, 10 parts by weight of Silicone Face, and boric acid. Lead 0.5
Parts by weight were added and kneaded using a roll mill at 90°C for 2 hours to obtain a printing ink. The ink prepared from the composition of Comparative Example 1 had a flow value of 18, a tank value of 9.0, and a critical surface tension of 20 dynes/tack; the ink prepared from the composition of Example 1 had a flow value of 18, a tack value of The value was 9.5, and the critical surface tension was 21 dynes/an.
これら両者の印刷インクを用い、常法に従いそれぞれア
ート紙1000枚ずつオフセット印Jiiifを行い、
12時間重ねて放置した。該時間経過後の裏うつりを調
べたところ、実施例1の組成物から調製した印刷インク
は裏うつりなく良好な結果を示しだが、比較例1の組成
物から調製した印刷インクは裏うつりがところどころで
起り、充分な裏うつり防止効果はなかった。Using both of these printing inks, perform offset printing Jiiif on 1000 sheets of art paper each according to the usual method,
It was left to overlap for 12 hours. When examining the back transfer after the lapse of this time, the printing ink prepared from the composition of Example 1 showed good results with no back transfer, but the printing ink prepared from the composition of Comparative Example 1 showed back transfer in some places. This occurred, and there was no sufficient effect to prevent the back from rolling.
図1にはグラインドメーター 図2にはスクレーパー(2種類) の例を示した。 以 ト Figure 1 shows the grind meter. Figure 2 shows scrapers (2 types) An example was shown. Below
Claims (1)
ンを混合、分散してなる印刷インク用組成物。 2、変性低分子量ポリテトラフルオロエチレンがテトラ
フルオロエチレン60〜99.999モル%ト含フッ素
α−オレフィンo、ooi〜40モル%との共重合体で
ある前記第1積重戦の印刷インク用組成物。[Claims] 1. A printing ink composition comprising a vehicle mixed with and dispersed with modified low molecular weight polytetrafluoroethylene. 2. For the printing ink of the first stack, wherein the modified low molecular weight polytetrafluoroethylene is a copolymer of 60 to 99.999 mol% of tetrafluoroethylene and 40 to 40 mol% of fluorine-containing α-olefin o, ooi. Composition.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58034209A JPS59159863A (en) | 1983-03-01 | 1983-03-01 | Composition for printing ink |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58034209A JPS59159863A (en) | 1983-03-01 | 1983-03-01 | Composition for printing ink |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59159863A true JPS59159863A (en) | 1984-09-10 |
JPH0347307B2 JPH0347307B2 (en) | 1991-07-18 |
Family
ID=12407763
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58034209A Granted JPS59159863A (en) | 1983-03-01 | 1983-03-01 | Composition for printing ink |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59159863A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62143983A (en) * | 1985-12-19 | 1987-06-27 | Toyo Ink Mfg Co Ltd | Printing ink |
JPS62143984A (en) * | 1985-12-19 | 1987-06-27 | Toyo Ink Mfg Co Ltd | Printing ink |
JPS62172078A (en) * | 1986-01-27 | 1987-07-29 | Dainichi Color & Chem Mfg Co Ltd | Printing ink composition |
JPS62172077A (en) * | 1986-01-27 | 1987-07-29 | Dainichi Color & Chem Mfg Co Ltd | Printing ink composition |
JPS62187775A (en) * | 1986-02-14 | 1987-08-17 | Toyo Ink Mfg Co Ltd | Addition for printing ink and printing ink obtained by using same |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS52125010A (en) * | 1976-04-12 | 1977-10-20 | Ricoh Kk | Composition of ink for lithographic printing |
JPS53128404A (en) * | 1977-04-15 | 1978-11-09 | Pentel Kk | Oily ink composition |
-
1983
- 1983-03-01 JP JP58034209A patent/JPS59159863A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS52125010A (en) * | 1976-04-12 | 1977-10-20 | Ricoh Kk | Composition of ink for lithographic printing |
JPS53128404A (en) * | 1977-04-15 | 1978-11-09 | Pentel Kk | Oily ink composition |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62143983A (en) * | 1985-12-19 | 1987-06-27 | Toyo Ink Mfg Co Ltd | Printing ink |
JPS62143984A (en) * | 1985-12-19 | 1987-06-27 | Toyo Ink Mfg Co Ltd | Printing ink |
JPH0562912B2 (en) * | 1985-12-19 | 1993-09-09 | Toyo Ink Mfg Co | |
JPH0562911B2 (en) * | 1985-12-19 | 1993-09-09 | Toyo Ink Mfg Co | |
JPS62172078A (en) * | 1986-01-27 | 1987-07-29 | Dainichi Color & Chem Mfg Co Ltd | Printing ink composition |
JPS62172077A (en) * | 1986-01-27 | 1987-07-29 | Dainichi Color & Chem Mfg Co Ltd | Printing ink composition |
JPS62187775A (en) * | 1986-02-14 | 1987-08-17 | Toyo Ink Mfg Co Ltd | Addition for printing ink and printing ink obtained by using same |
JPH0579112B2 (en) * | 1986-02-14 | 1993-11-01 | Toyo Ink Mfg Co |
Also Published As
Publication number | Publication date |
---|---|
JPH0347307B2 (en) | 1991-07-18 |
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