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Tentative Mechanisms for In Situ Polymerization of Metanilic Acid Intercalated in MgAl Layered Double Hydroxide under Nitrogen Atmosphere

机译:在氮气氛下MgAl层层双氢氧化物中嵌入甲硅酸的原位机制

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A new route has been developed to prepare polyaniline (PANI)/ layered double hydroxides (LDHs) nanocomposites through in situ chemical oxidative polymerization of metanilic acid (m-NH_2C_6H_4SO_3H) intercalated in MgAl LDH under nitrogen atmosphere by using the pre-intercalated nitrate as the oxidizing agent. The whole process involves the synthesis of the precursor LDHs [Mg_2Al (OH)_6](NO_3)-nH_2O, the intercalation of the monomer metanilic acid into LDH and its in situ polymerization between the layers by thermal treatment under nitrogen atmosphere. The interlayer polymerization was monitored by thermogravimetry (TG)-differential thermal analysis (DTA) - mass spectrometry (MS), UV-vis spectroscopy and in situ high temperature X-ray diffraction (HT-XRD). UV-vis spectroscopy give strong evidence on the polymerization of the intercalated metanilic acid, with the increase of the interlayer distance and broadening of the diffraction peaks. It has been found by the in situ technologies that the co-intercalated nitrate anions act as the oxidizing agent which participate in the polymerization of the interlayer monomers under nitrogen atmosphere by heating from 300°C to 350°C.
机译:通过在氮气氛下在的MgAl LDH嵌入间氨基苯甲酸(m-NH_2C_6H_4SO_3H)的原位化学氧化聚合的新路径已经被开发,以制备聚苯胺(PANI)/层状双氢氧化物(水滑石)纳米复合材料,通过使用所述预插层硝酸盐作为氧化剂。整个过程包括水滑石前体的合成[Mg_2Al(OH)_6](NO_3)-nH_2O,单体间胺酸的嵌入到LDH以及各层之间通过热处理在氮气氛下其原位聚合。中间层聚合反应通过热重(TG) - 示差热分析(​​DTA)来监测 - 质谱法(MS),紫外可见光谱和原位高温X射线衍射(HT-XRD)。紫外 - 可见的插层间胺酸的聚合上光谱给予了强有力的证据,与层间距离的增加和衍射峰的加宽。已经发现通过原位技术,共插硝酸根阴离子作为其通过加热从300℃至350℃参与氮气氛下在层间单体的聚合中的氧化剂。

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