Cross-linking agent as well as preparation method and application thereof
A cross-linking agent and reaction technology, applied in the field of cross-linking agent and its preparation, can solve the problems of printing force plate-making contrast, increase environmental protection pressure, low chemical development or on-machine development ability, etc., achieve strong hydrolysis resistance, improve Imaging ability, green development effect
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[0032] The raw materials for the preparation of the crosslinking agent include dicyclohexylmethane diisocyanate, dibutyltin dilaurate, ethyl-3-oxetanemethanol and ε-caprolactam. Since the synthesized cross-linking agent is a specific compound, it is enough to synthesize the specific compound according to the raw material, and the ratio of the raw material will only affect the yield of the product.
[0033]The preparation method of the cross-linking agent, the preparation method of the cross-linking agent, heating dicyclohexylmethane diisocyanate, dibutyltin dilaurate, and solvent to 35°C-80°C, adding ethyl-3-oxetane dropwise Cyclomethanol was reacted, and then ε-caprolactam was added to react until the peak at 2275 of the active isocyanate group detected by infrared spectroscopy disappeared, and a solution containing a crosslinking agent was obtained.
[0034] The preparation method of the crosslinking agent comprises heating dicyclohexylmethane diisocyanate, dibutyltin dilaur...
Embodiment 1
[0064] Example 1 (special thermosensitive resin L1)
[0065] Add 300g of dimethylacetamide, 80g (80% by weight) of methacrylamide, 10g (10% by weight) of hydroxyethyl acetamide to a 500ml four-necked flask equipped with temperature-controlled heating, mechanical stirring, reflux and nitrogen protection. Acrylamide, 10g (10% by weight) of 3,4-epoxycyclohexyl methacrylate, and 1g of azobisisobutyronitrile were stirred evenly, and reacted at 70°C for 8 hours, and the reaction was completed by cooling down, and the reaction stock solution could be used directly.
Embodiment 2
[0066] Example 2 (special thermosensitive resin L2)
[0067] Add 300g of dimethylacetamide, 70g (70% by weight) of methacrylamide, 20g (20% by weight) of hydroxyethyl methacrylamide to a 500ml four-necked flask with temperature-controlled heating, mechanical stirring, condensing reflux and nitrogen protection device Acrylamide, 10g (10% by weight) of 3,4-epoxycyclohexyl methacrylate, and 1g of azobisisobutyronitrile were stirred evenly, and reacted at 70°C for 8 hours, and the reaction was completed by cooling down, and the reaction stock solution could be used directly.
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