Controlled reactivity of metastable n-Al@Bi(IO3)3 by employment of tea polyphenols as an interfacial layer

Deyun Tang, Shuwen Chen, Xiaolian Liu, Wei He, Guangcheng Yang, Pei Jin Liu, Michael Gozin, Qi Long Yan

科研成果: 期刊稿件文章同行评审

49 引用 (Scopus)

摘要

It has been demonstrated in this paper that the tea polyphenols (TP) can easily adhere to the surface of particles through self-polymerization, even these particles are very hydrophobic. In this paper, a method of in-situ polymerization of TP has been used to coat n-Al powder. Then, Bi(IO3)3 crystal is grown on TP as an interfacial layer to obtain core-shell iodine-based MICs (n-Al@TP@Bi(IO3)3). Various characterization techniques are used to investigate the prepared core-shell MICs, including scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), thermal analysis, mass spectrum (MS), bomb calorimetry and high-speed camera. The results show that the obtained novel MICs are uniformly and densely distributed. The n-Al@TP@Bi(IO3)3 has higher reactivity and heat release than the traditional mechanical mixture, and the initial reaction temperature is reduced by about 30 °C caused by the decomposition-promoting effect of the decomposition product of TP (carbon) on Bi(IO3)3. and the volume reaction heat of n-Al@TP@Bi(IO3)3 (21.246 kJ cm−3) enhances by 11.3%. The results of combustion experiments show that the burning rate of n-Al@TP@Bi(IO3)3 is above 3.4 m s−1, which is 4 times that of Al/ Bi(IO3)3 (0.9 m s−1). Moreover, the combustion efficiency is higher and the agglomeration of the condensed combustion products is greatly decreased. Various other core-shell structured MICs with tunable reactivity could be easily prepared by using similar interfacial binding materials by using our strategy as a guidance.

源语言英语
文章编号122747
期刊Chemical Engineering Journal
381
DOI
出版状态已出版 - 1 2月 2020

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