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Modification of chitosan for preparation of poly(N-isopropylacrylamide/udO-nitrochitosan) interpenetrating polymer network

机译:壳聚糖改性制备聚(N-异丙基丙烯酰胺/ ud)邻硝基壳聚糖)互穿聚合物网络

摘要

An interpenetrating polymer network (IPN), N-isopropylacrylamide/O-nitrochitosan (NONK) was developed in the presence of ammonium persulfate using solution polymerization technique. O-nitrochitosan (ONK) was synthesized from chitosan, before it was further reacted with N-isopropylacrylamide. A new vibration of the C-N bond formed between the NH from ONK and the CH2 from NIPAAm was detected at the peak 1154 and 1171 cm-1 using attenuated total reflection Fourier-transform infrared (ATR-FTIR) spectroscopy. In the polymerization, the primary amine became a secondary amine and the peaks of the amide I (C=O peak) and amide II (N–H) were broadened. The structure of ONK was confirmed using nuclear magnetic resonance (NMR). At 10°C, the result from swelling test was found that IPN poly(NONK82) had the highest swelling percentage, 1171%, compared to poly (NIPAAm) at 467%. Micrograph from scanning electron microscopy (SEM) indicated the pore size of IPN NONK increased with an increasing ratio of ONK.
机译:使用溶液聚合技术,在过硫酸铵存在下,开发了一种互穿聚合物网络(IPN)N-异丙基丙烯酰胺/ O-硝基壳聚糖(NONK)。由壳聚糖合成邻硝基壳聚糖(ONK),然后使其与N-异丙基丙烯酰胺进一步反应。使用衰减全反射傅立叶变换红外(ATR-FTIR)光谱在1154和1171 cm-1峰处检测到ONK的NH和NIPAAm的CH2之间形成的C-N键的新振动。在聚合反应中,伯胺变为仲胺,酰胺I(C = O峰)和酰胺II(NH)的峰变宽。使用核磁共振(NMR)证实了ONK的结构。在10°C时,溶胀试验的结果发现,与聚(NIPAAm)的467%相比,IPN聚(NONK82)的溶胀百分比最高,为1171%。扫描电子显微镜(SEM)的显微照片表明IPN NONK的孔径随ONK比例的增加而增加。

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