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通过原子转移自由基聚合(ATRP)将丙烯酰胺聚合物套在细菌纤维素纳米纤维上得到的纳米结构复合材料。

Nanostructured composites obtained by ATRP sleeving of bacterial cellulose nanofibers with acrylate polymers.

机构信息

CICECO and Chemistry Department, University of Aveiro , Campus de Santiago, 3810-193 Aveiro, Portugal.

出版信息

Biomacromolecules. 2013 Jun 10;14(6):2063-73. doi: 10.1021/bm400432b. Epub 2013 May 21.

Abstract

Novel nanostructured composite materials based on bacterial cellulose membranes (BC) and acrylate polymers were prepared by in situ atom transfer radical polymerization (ATRP). BC membranes were functionalized with initiating sites, by reaction with 2-bromoisobutyryl bromide (BiBBr), followed by atom transfer radical polymerization of methyl methacrylate (MMA) and n-butyl acrylate (BA), catalyzed by copper(I) bromide and N,N,N',N″,N″-pentamethyldiethylenetriamine (PMDETA), using two distinct initiator amounts and monomer feeds. The living characteristic of the system was proven by the growth of PBA block from the BC-g-PMMA membrane. The BC nanofiber sleeving was clearly demonstrated by SEM imaging, and its extent can be tuned by controlling the amount of initiating sites and the monomer feed. The ensuing nanocomposites showed high hydrophobicity (contact angles with water up to 134°), good thermal stability (initial degradation temperature in the range 241-275 °C), and were more flexible that the unmodified BC membranes.

摘要

新型纳米结构复合基于细菌纤维素膜(BC)和丙烯酸酯聚合物的材料是通过原位原子转移自由基聚合(ATRP)制备的。BC 膜通过与 2-溴异丁酰溴(BiBBr)反应,在引发剂位点上进行功能化,然后在铜(I)溴化物和 N,N,N',N'',N''-五甲基二亚乙基三胺(PMDETA)的催化下,进行甲基丙烯酸甲酯(MMA)和正丁基丙烯酸酯(BA)的原子转移自由基聚合,使用两种不同的引发剂用量和单体进料。通过从 BC-g-PMMA 膜生长 PBA 嵌段证明了该体系的活性特征。BC 纳米纤维套管通过 SEM 成像清晰地显示出来,并且可以通过控制引发剂用量和单体进料来调节其程度。随后的纳米复合材料表现出高疏水性(与水的接触角高达 134°),良好的热稳定性(初始降解温度在 241-275°C 范围内),并且比未改性的 BC 膜更具柔韧性。

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