首页|FeCo2O4催化TKX-50的分解特性及其热动力学分析

FeCo2O4催化TKX-50的分解特性及其热动力学分析

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为研究双金属氧化剂作为燃烧催化剂在推进剂方面的应用,基于水热法制备了双金属氧化剂FeCo2O4,并采用扫描电子显微镜(SEM)、N2吸脱附测试(BET)、X射线衍射分析(XRD)和X射线光电子能谱分析(XPS)对催化剂的理化性质进行了表征.通过同步热分析仪(TG-DSC)研究了该氧化剂对5,5'-联四唑-1,1'-二氧二羟胺(TKX-50)的催化分解特性及热分解反应动力学参数的影响.结果表明,双金属氧化剂FeCo2O4 的加入明显促进了TKX-50 的热分解行为,随着双金属氧化剂含量的增加,升温速率为10.0℃·min-1时,复合材料的两个放热峰峰值温度都呈现减小的趋势,最大分别减少了34.0℃和49.7℃.添加双金属氧化剂还会降低复合体系的表观活化能与活化焓值,TKX-50热力学特征参数的降低,证实了双金属氧化剂燃烧催化剂的潜质.
Catalytic Decomposition Characteristics and Thermodynamic Analysis of TKX-50 by FeCo2O4
In order to study the application of bimetallic oxidants as combustion catalysts in propellants,a bimetallic oxidant FeCo2O4 was prepared using hydrothermal method.The physical and chemical proper-ties of the catalyst were characterized using scanning electron microscopy(SEM),N2 adsorption and desorption testing(BET),X-ray diffraction analysis(XRD)and X-ray photoelectron spectroscopy(XPS).The catalytic decomposition characteristics and thermal decomposition reaction kinetics param-eters of 5,5'-tetrazol-1,1'-dioxodihydroxylamine(TKX-50)were studied using a synchronous thermal analyzer(TG-DSC).The results showed that the addition of bimetallic oxidant FeCo2O4 significantly pro-motes the thermal decomposition behavior of TKX-50.With the increase of bimetallic oxidant content,at 10.0℃·min-1 of the heating rate,the peak temperatures of the two exothermic peaks of the composite material show a decreasing trend,with maximum reductions of 34.0℃and 49.7℃,respectively.The addition of bimetallic oxidants also reduces the apparent activation energy and activation enthalpy of the composite system.The decrease in the thermodynamic characteristic parameters of TKX-50 confirms the potential of bimetallic oxidant combustion catalysts.

bimetallic oxideTKX-50TG-DSCthermodynamic parametersthermal decomposition

翟安琪、赵海霞、张军梅、郭璟昊、赵碧颖

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中北大学 环境与安全工程学院,山西 太原 030051

陕西应用物理化学研究所,陕西 西安 710061

双金属氧化物 TKX-50 TG-DSC 热动力学参数 热分解

中北大学重点实验室开放研究基金资助项目

DXMBJJ2021-01

2024

中北大学学报(自然科学版)
中北大学

中北大学学报(自然科学版)

影响因子:0.258
ISSN:1673-3193
年,卷(期):2024.45(3)