Jin Gong, T. Miyazaki, Kohei Takahashi, Y. Mao, M. Sugimoto
{"title":"Polymer Gel Fibers Produced by UV-Reactive Electrospinning","authors":"Jin Gong, T. Miyazaki, Kohei Takahashi, Y. Mao, M. Sugimoto","doi":"10.2115/fiberst.2020-0040","DOIUrl":null,"url":null,"abstract":": A potentially effective method to prepare fibers of polymer gels with chemically crosslinked structure using ultraviolet (UV)-reactive electrospinning (UV-ES) is demonstrated. The UV-ES method makes sure the polymerization (i. e., gelation) proceeds simultaneously with the spinning process through employing an UV irradiator between the nozzle and the target (fiber collector). The fiber manufacturing via UV-ES succeeded for both polymer gels of poly(N, N-dimethylacrylamide) (G(DMAA)) and poly(DMAA-stearyl acrylate-dodecyl acrylate) (G(DMAA-SA-DA)). It is found that the viscosity of gel reactions influences the fiber diameter greatly. Higher viscosity generally tends to result in an increase in diameter of fibers regardless of the electric field intensity. Depending on the spinning conditions, G(DMAA) fibers with a diameter ranging 2 nm ~ 5.5 µ m, and G(DMAA-SA-DA) fibers with a diameter ranging 30~100 µ m are produced. The FTIR measurement for the resultant G(DMAA) and G(DMAA-SA-DA) fibers illustrates the polymerization essentially completed while spinning the fibers. This study highlights the potential possibilities of the UV-ES method in practical fiber-manufacturing applications for polymer gels.","PeriodicalId":54299,"journal":{"name":"Journal of Fiber Science and Technology","volume":" ","pages":""},"PeriodicalIF":0.3000,"publicationDate":"2020-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Fiber Science and Technology","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.2115/fiberst.2020-0040","RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"MATERIALS SCIENCE, TEXTILES","Score":null,"Total":0}
引用次数: 2
Abstract
: A potentially effective method to prepare fibers of polymer gels with chemically crosslinked structure using ultraviolet (UV)-reactive electrospinning (UV-ES) is demonstrated. The UV-ES method makes sure the polymerization (i. e., gelation) proceeds simultaneously with the spinning process through employing an UV irradiator between the nozzle and the target (fiber collector). The fiber manufacturing via UV-ES succeeded for both polymer gels of poly(N, N-dimethylacrylamide) (G(DMAA)) and poly(DMAA-stearyl acrylate-dodecyl acrylate) (G(DMAA-SA-DA)). It is found that the viscosity of gel reactions influences the fiber diameter greatly. Higher viscosity generally tends to result in an increase in diameter of fibers regardless of the electric field intensity. Depending on the spinning conditions, G(DMAA) fibers with a diameter ranging 2 nm ~ 5.5 µ m, and G(DMAA-SA-DA) fibers with a diameter ranging 30~100 µ m are produced. The FTIR measurement for the resultant G(DMAA) and G(DMAA-SA-DA) fibers illustrates the polymerization essentially completed while spinning the fibers. This study highlights the potential possibilities of the UV-ES method in practical fiber-manufacturing applications for polymer gels.
介绍了一种利用紫外-反应静电纺丝(UV- es)制备具有化学交联结构的聚合物凝胶纤维的有效方法。UV- es方法通过在喷嘴和目标(纤维收集器)之间使用紫外线照射器,确保聚合(即凝胶化)与纺丝过程同时进行。紫外分光光度法成功制备了聚(N, N-二甲基丙烯酰胺)(G(DMAA))和聚(DMAA-丙烯酸硬脂酯-丙烯酸十二酯)(G(DMAA- sa - da))聚合物凝胶。结果表明,凝胶反应的粘度对纤维直径影响较大。无论电场强度如何,较高的粘度通常会导致纤维直径的增加。根据纺丝条件的不同,可生产直径为2nm ~ 5.5µm的G(DMAA)纤维和直径为30~100µm的G(DMAA- sa - da)纤维。对合成的G(DMAA)和G(DMAA- sa - da)纤维的FTIR测量表明,聚合基本上是在纤维纺丝时完成的。这项研究强调了紫外光谱法在聚合物凝胶纤维制造中的潜在应用。