Inhibition of sucrose dust deflagration by carbonate and kinetic study by thermal analysis

蔗糖 粉尘爆炸 碳酸盐 化学 动能 分解 热分解 燃烧 化学工程 核化学 有机化学 物理 量子力学 工程类
作者
Guowei Chen,Kaili Xu,Jishuo Li,Bo Liu,Lu Sun,Jingwen wen
出处
期刊:Journal of Loss Prevention in The Process Industries [Elsevier BV]
卷期号:90: 105358-105358
标识
DOI:10.1016/j.jlp.2024.105358
摘要

To prevent the explosion of sucrose dust, the ability of carbonate powders as a sucrose dust explosion inhibitor is systematically analyzed and compared. The explosion inhibition effect of carbonate powders on sucrose dust is investigated by means of minimum ignition energy (MIE) and 20L sphere explosion experiments. The results indicate that as the amount of carbonate powder added increased, sucrose dust explosion can be completely inhibited. Compared with CaCO3, KHCO3, and NH4HCO3, the inhibitory ability of NaHCO3 is 25.00%, 40.00%, and 57.14% better for MIE and 25.00%, 33.33%, and 50% better for explosion properties. The kinetic model of thermal decomposition of sucrose dust before and after NaHCO3 intervention was comparatively analyzed and validated using Coats-Redfern (C - R) and Kissinger - Akahira - Sunose (KAS) methods. The kinetic modeling of the thermal decomposition of sucrose dust before and after the addition of NaHCO3 was found to follow the chemical reaction mechanism (F4 model). Further fitting analysis demonstrates that after adding NaHCO3 inhibitor, the apparent activation energy of sucrose dust is greatly increased, further confirming that carbonate powders can greatly inhibit sucrose dust explosion on thermodynamic terms. Finally, based on the characterization result, the inhibitory mechanisms of carbonates on sucrose dust explosion are proposed and two reasons explaining why NaHCO3 has better inhibitory ability than CaCO3, KHCO3, and NH4HCO3 are summarized. One is that the decomposition of NaHCO3 is a highly heat-absorbing process during which part of the heat produced by the combustion of sucrose dust is absorbed. The other is that NaHCO3 and its product have small particle sizes but large specific surface areas, consequently higher unit heat absorption capacity and better dispersivity.
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