Lithographic printing plate precursor
一种平版印刷版、前驱体的技术,应用在平版印刷设备、印刷、印刷工艺等方向,能够解决重启着色没有效果等问题,达到着色恢复性良好、良好油墨清洗特性的效果
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[0191] Hereinafter, the present invention will be described in more detail as one aspect based on an example of a lithographic printing plate having a positive image-forming layer. However, the present invention is not limited to these examples. Obviously, the present invention may also be a lithographic printing plate precursor having a negative image forming layer as another aspect.
[0192]
Synthetic example 1
[0193] Synthesis Example 1 Vinylphosphonic acid / acrylamide copolymer (molar ratio 1:9) (I-1)
[0194] Add 3500 g of ethanol to a 10-liter flask equipped with a stirrer, a condenser, and a dropping device, and heat to 70° C. 231.1 g (2.14 mol) of vinylphosphonic acid monomer, 1368.9 g (19.26 mol) of acrylamide, and 52 g of AIBN were dissolved in 1000 g of ethanol, and the solution was added dropwise to the reaction device over 4 hours. During the dropwise addition of the monomer solution, a white precipitate was formed. After further heating and stirring at 70° C. for 2 hours, the heating was stopped and cooled to room temperature. The resulting precipitate was collected by filtration under reduced pressure and washed with 1000 g of ethanol. Vacuum drying at 40°C for 24 hours yielded white microcrystals. Yield 1550g
Synthetic example 2
[0195] Synthesis example 2 Vinylphosphonic acid / acrylamide copolymer (molar ratio 2:8) (I-2)
[0196] Add 3500 g of ethanol to a 10-liter flask equipped with a stirrer, a condenser, and a dropping device, and heat to 70° C. 440.5 g (4.08 mol) of vinylphosphonic acid monomer, 1159.5 g (16.31 mol) of acrylamide, and 52 g of AIBN were dissolved in 1000 g of ethanol, and the solution was added dropwise to the reaction device over 4 hours. During the dropwise addition of the monomer solution, a white precipitate was formed. After further heating and stirring at 70° C. for 2 hours, the heating was stopped and cooled to room temperature. The resulting precipitate was collected by filtration under reduced pressure and washed with 1000 g of ethanol. Vacuum drying at 40°C for 24 hours yielded white microcrystals. Yield 1550g
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