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通过表面引发的原子转移自由基聚合反应从纳米多孔纤维素凝胶接枝以制备疏水性纳米复合材料。

Surface-initiated atom transfer radical polymerization grafting from nanoporous cellulose gels to create hydrophobic nanocomposites.

作者信息

Cheng Dan, Wei Pingdong, Zhang Lina, Cai Jie

机构信息

College of Chemistry and Molecular Sciences, Wuhan University Wuhan 430072 China

Research Institute of Shenzhen, Wuhan University Shenzhen 518057 China.

出版信息

RSC Adv. 2018 Jul 31;8(48):27045-27053. doi: 10.1039/c8ra04163f. eCollection 2018 Jul 30.

Abstract

Here, we present the preparation of hydrophobic nanoporous cellulose gel--poly(glycidyl methacrylate) (NCG--PGMA) nanocomposites by surface-initiated atom transfer radical polymerization (SI-ATRP) of glycidyl methacrylate (GMA) monomers and hydrophobic modification with pentadecafluorooctanoyl chloride (CFCOCl) on the cellulose nanofibrils of the NCG. The successful grafting of PGMA and hydrophobic modification of CFCO- groups on the NCG was evaluated by Fourier transform infrared (FTIR) spectroscopy. X-ray diffraction (XRD) and scanning electron microscopy (SEM) confirmed that the SI-ATRP and hydrophobic modification did not change the microscopic morphology and structure of the NCG--PGMA nanocomposites. Dynamic mechanical analysis (DMA) and thermogravimetric analysis (TGA) showed remarkable thermomechanical properties and moderate thermal stability. The method has tremendous promise to use NCG as a platform for SI-ATRP and produce new functional NCG-based nanomaterials.

摘要

在此,我们展示了通过甲基丙烯酸缩水甘油酯(GMA)单体的表面引发原子转移自由基聚合(SI-ATRP)以及在纳米纤维素凝胶(NCG)的纤维素纳米原纤上用十五氟辛酰氯(CFCOCl)进行疏水改性来制备疏水性纳米多孔纤维素凝胶-聚(甲基丙烯酸缩水甘油酯)(NCG-PGMA)纳米复合材料。通过傅里叶变换红外(FTIR)光谱对PGMA的成功接枝以及CFCO-基团在NCG上的疏水改性进行了评估。X射线衍射(XRD)和扫描电子显微镜(SEM)证实,SI-ATRP和疏水改性并未改变NCG-PGMA纳米复合材料的微观形态和结构。动态力学分析(DMA)和热重分析(TGA)表明其具有显著的热机械性能和适度的热稳定性。该方法极有希望将NCG用作SI-ATRP的平台,并生产新型功能性NCG基纳米材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db9b/9083290/0b19110f5418/c8ra04163f-f1.jpg

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