Lithographic printing plate precursor and process for producing lithographic printing plate
A technology for lithographic printing plates and production methods, which is applied in lithographic printing equipment, printing, printing technology, etc., can solve the problems of narrow development latitude and other problems, and achieve high printing resistance, good scratch resistance, and wide development latitude Effect
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[0171] Hereinafter, the present invention will be described in more detail using examples, but the present invention is not limited to the scope of these examples.
Synthetic example 1
[0173] 29.1 g of 4,4'-diphenylmethane diisocyanate, 20.2 g of toluene-2,4-diisocyanate, and 6.3 g of neopentyl diisocyanate were introduced into a 500-ml round-bottomed three-necked flask equipped with a concentrator and a stirrer. Diol, 23.7 g of 2,2-bis(hydroxymethyl)propionic acid, 10.7 g of polyneopentyl glycol having a fluorine group represented by the structural formula shown below, and 270 g of 3-pentanone. 0.3 g of dibutyltin dilaurate was added, and it heated to 80 degreeC, stirring a reaction mixture. The reaction was continued at 80°C for 6 hours. Polyurethane (1) is thus obtained. The weight average molecular weight obtained by GPC was 22,000. The acid value is 110.
[0174] [chemical 13]
[0175] the
[0176] Polyneopentyl glycol having a fluorine group.
Synthetic example 2~11
[0178] Polyurethanes (2) to (11) were obtained in the same manner as in Synthesis Example 1 except that the diisocyanate and diol shown in Table 1 were used.
[0179] [Table 1-1]
[0180]
[0181]
[0182]
[0183]
[0184] .
[0185]
[0186] [Invention Example 1]
[0187]
[0188] The surface of the aluminum sheet is subjected to electrolytic surface roughening treatment with 2% hydrochloric acid. The average roughness Ra was 0.5 μm. Furthermore, anodic oxidation treatment was carried out in 20% sulfuric acid aqueous solution so that the amount of oxide film was 2.7g / m 2 . Then, the anodized aluminum sheet was immersed in a 2.5% by weight sodium silicate aqueous solution at 70° C. for 30 minutes, washed with water, and then dried.
[0189]
[0190] On the substrate obtained as above, the underlayer coating solution 1 shown in Table 2 was coated with a bar coater so that the coating weight was 1.4 g / m 2 , after drying at 135°C for 40 seconds, cooled t...
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