Abstract: 
										[Objective]In order to reduce the curing temperature of polyimide(PI)system and to ensure its reaction controllability and storage stability.[Methods]This study synthesized a biomass-derived thymine-based photobase generator,thymine-1-acetic acid diazabicyclononene salt(TY-DBN),and applied it to cure polyamic acid resin coatings.[Results]TY-DBN released the superbase 1,5-diazabicyclo[4. 3. 0]-5-nonene(DBN)under UV irradiation. The curing kinetics demonstratedthat the optimal curing temperature decreased from 197. 00 ℃ to 60. 11 ℃,the apparent activation energy was reduced by two orders of magnitude(from 4. 49×104 J/mol to 6. 57×102 J/mol), and the reaction order decreased from 0. 93 to 0. 28. Normalized infrared spectroscopy confirmed a significantincrease in the imidization degree of the coating resin after low-temperature curing.[Conclusion]This study significantly improved the thermal curing performance of polyamic acid resin,providing a research strategy for developing low-temperature curable polyimide coating.
									
																									Key words: 
																																						   photobase generator, 
																																							   thymine, 
																																							   polyimide, 
																																							   low-temperature curing 
																												
																								摘要: 【目的】为了降低聚酰亚胺( PI)体系固化温度,且保证其反应可控性和贮存稳定性。【方法】合成了基于生物质胸腺嘧啶的光产碱剂胸腺嘧啶 .1-乙酸重氮双环壬烯盐( TY-DBN)并应用于聚酰胺酸树脂涂层的固化。【结果】 TY-DBN经紫外光辐照可释放超强碱 1,5-二氮杂双环 [4. 3. 0]-5-,壬烯( DBN)固化动力学研究表明,聚酰胺酸树脂最佳固化温度由 197. 00 ℃降低至 60.11 ℃,表观活化能降低 2个数,量级,由 4. 49×104 J/mol降至 6. 57×102 J/mol,反应级数由 0. 93降至 0. 28。且归一化红外表征证实涂层在低温固化后酰亚胺化程度显著提升。【结论】本研究显著改善了聚酰胺酸树脂的热固化性能,为开发低温固化聚酰亚胺涂层提供研究思路。
																								关键词: 
								   																																   光产碱剂, 
																																											   胸腺嘧啶, 
																																											   聚酰亚胺, 
																																											   低温固化 
																													
															
                            
                                                        	
								
								CLC Number: