粘接
粘接
점접
2014年
10期
35-38
,共4页
郝锐颖%陈凡%张军营%程珏
郝銳穎%陳凡%張軍營%程玨
학예영%진범%장군영%정각
稀释剂%实时红外%双固化%聚硅氧烷丙烯酸酯%固化顺序
稀釋劑%實時紅外%雙固化%聚硅氧烷丙烯痠酯%固化順序
희석제%실시홍외%쌍고화%취규양완병희산지%고화순서
diluent%FT-IR%dual-curing%polysiloxane acrylate%curing sequence
添加活性稀释剂是调节光固化体系黏度、光固化反应速率、固化产物性能的有效手段。采用丙烯酸异辛酯2-EHA 为活性稀释剂,利用实时红外(FT-IR)研究了活性稀释剂用量对双固化聚硅氧烷丙烯酸酯树脂(PSA)光聚合的影响。结果表明,稀释剂的加入不仅能改善体系的流变性能,同时稀释剂参与光聚合过程,提高体系的固化交联程度,改变交联网络,从而影响固化物的力学性能。通过红外跟踪研究了固化顺序(先光固化后湿气固化和先湿气固化后光固化)对体系中C=C双键和Si-OCH 基团转化率的影响,结果表明,先光后湿的3固化顺序更有利于使体系达到高的转化率;DSC分析发现固化顺序对固化物玻璃化转变温度有一定影响。
添加活性稀釋劑是調節光固化體繫黏度、光固化反應速率、固化產物性能的有效手段。採用丙烯痠異辛酯2-EHA 為活性稀釋劑,利用實時紅外(FT-IR)研究瞭活性稀釋劑用量對雙固化聚硅氧烷丙烯痠酯樹脂(PSA)光聚閤的影響。結果錶明,稀釋劑的加入不僅能改善體繫的流變性能,同時稀釋劑參與光聚閤過程,提高體繫的固化交聯程度,改變交聯網絡,從而影響固化物的力學性能。通過紅外跟蹤研究瞭固化順序(先光固化後濕氣固化和先濕氣固化後光固化)對體繫中C=C雙鍵和Si-OCH 基糰轉化率的影響,結果錶明,先光後濕的3固化順序更有利于使體繫達到高的轉化率;DSC分析髮現固化順序對固化物玻璃化轉變溫度有一定影響。
첨가활성희석제시조절광고화체계점도、광고화반응속솔、고화산물성능적유효수단。채용병희산이신지2-EHA 위활성희석제,이용실시홍외(FT-IR)연구료활성희석제용량대쌍고화취규양완병희산지수지(PSA)광취합적영향。결과표명,희석제적가입불부능개선체계적류변성능,동시희석제삼여광취합과정,제고체계적고화교련정도,개변교련망락,종이영향고화물적역학성능。통과홍외근종연구료고화순서(선광고화후습기고화화선습기고화후광고화)대체계중C=C쌍건화Si-OCH 기단전화솔적영향,결과표명,선광후습적3고화순서경유리우사체계체도고적전화솔;DSC분석발현고화순서대고화물파리화전변온도유일정영향。
The reactive diluents can adjust the viscosity and curing rate of the UV curing system and the performance of UV cured product. The influences of diluent contents on dual-curable polysiloxane acrylate resin (PSA) system photopolymerization were studied by FT-IR. The results showed that the addition of diluents not only improved the rheological properties of systems but participated in the photopolymerization process, enhanced the mechanical properties by increasing the crosslinking degree and modulating cross-linked network. Different curing sequences were investigated and the results showed that the variation of curing sequences had great influence on the conversion of double bonds (C=C) and methoxy groups (Si-OCH ), and the moisture curing after UV exposure gave a relatively higher conversion. The curing3 product of different curing order was evaluated by DSC, and it was demonstrated that the curing sequences had a certain degree of influence on the glass transition temperature.