化工学报
化工學報
화공학보
CIESC Jorunal
2015年
11期
4696-4702
,共7页
侧基叔胺二元醇%亲水性%UV固化阴极电泳涂料%乳液%粒度分布%合成
側基叔胺二元醇%親水性%UV固化陰極電泳塗料%乳液%粒度分佈%閤成
측기숙알이원순%친수성%UV고화음겁전영도료%유액%립도분포%합성
diol with pendent tertiary amine%hydrophilcity%UV-curable cathodic electrophoretic coatings%emulsions%size distribution%synthesis
将叔胺位于主链的 N-甲基二乙醇胺(MDEA)和叔胺位于侧基的7,12-二氧-3,16-二氮-3,16-二乙基-5,14-十八二醇(DDDOD)分别作为亲水单体,与聚己内酯二元醇(PCL)、异佛尔酮二异氰酸酯(IPDI)等反应,制备聚氨酯分散体。通过聚氨酯的分散性、分散体平均粒径,比较了亲水基位于聚氨酯主链和侧基的两种单体的亲水性。结果表明,亲水基团位于侧基时,亲水效果比位于主链的好。将叔氨基位于侧基的单体DDDOD作为亲水单体,与PCL、IPDI反应,制备了聚氨酯,加入UV固化单体,分散得到UV固化的阴极电泳涂料。研究了涂料的乳液性能和UV固化后双键转化率和膜性能。
將叔胺位于主鏈的 N-甲基二乙醇胺(MDEA)和叔胺位于側基的7,12-二氧-3,16-二氮-3,16-二乙基-5,14-十八二醇(DDDOD)分彆作為親水單體,與聚己內酯二元醇(PCL)、異彿爾酮二異氰痠酯(IPDI)等反應,製備聚氨酯分散體。通過聚氨酯的分散性、分散體平均粒徑,比較瞭親水基位于聚氨酯主鏈和側基的兩種單體的親水性。結果錶明,親水基糰位于側基時,親水效果比位于主鏈的好。將叔氨基位于側基的單體DDDOD作為親水單體,與PCL、IPDI反應,製備瞭聚氨酯,加入UV固化單體,分散得到UV固化的陰極電泳塗料。研究瞭塗料的乳液性能和UV固化後雙鍵轉化率和膜性能。
장숙알위우주련적 N-갑기이을순알(MDEA)화숙알위우측기적7,12-이양-3,16-이담-3,16-이을기-5,14-십팔이순(DDDOD)분별작위친수단체,여취기내지이원순(PCL)、이불이동이이청산지(IPDI)등반응,제비취안지분산체。통과취안지적분산성、분산체평균립경,비교료친수기위우취안지주련화측기적량충단체적친수성。결과표명,친수기단위우측기시,친수효과비위우주련적호。장숙안기위우측기적단체DDDOD작위친수단체,여PCL、IPDI반응,제비료취안지,가입UV고화단체,분산득도UV고화적음겁전영도료。연구료도료적유액성능화UV고화후쌍건전화솔화막성능。
N-Methyldiethanolamine (MDEA) bearing main chain tertiary amine and 7,12-dioxa-3,16-diaza- 3,16-diethyl-5,14-octadecanediol (DDDOD) bearing pendant tertiary amine were used as the hydrophilic monomers, respectively to prepare polyurethane dispersions. Hydrophilcity of the two hydrophilic monomers was compared by the dispersibilities of the polyurethanes and mean diameters of the dispersions. The results showed that DDDOD had a better hydrophilcity than MDEA, revealing that hydrophilic monomer with pendant tertiary amine had a superior hydrophilic ability than that with backbone tertiary amine. Polyurethane was prepared by the reaction between DDDOD, poly-caprolaclone glycol(PCL) and isophorone diisocyanate (IPDI). UV-curable monomers were added into the polyurethane and dispersed together. The properties of the dispersions and films were studied. The conversion of carbon-carbon double bonds after UV-curing was analyzed.