葡萄糖超临界水气化过程中总有机碳破坏的动力学研究

IF 1.5 4区 化学 Q4 CHEMISTRY, PHYSICAL
Muhammad Badrul Islam Chowdhury, Md Zakir Hossain, Paul A. Charpentier
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引用次数: 0

摘要

在 400-500°C 和 25 兆帕的条件下,在一个 600 毫升的间歇式反应器中研究了葡萄糖超临界水气化(SCWG)过程中总有机碳(TOC)的破坏动力学。TOC 和水的浓度对于 TOC 在超临界水中的转化至关重要,尤其是在停留时间较长的情况下。起初,人们认为 TOC 破坏反应遵循一阶动力学,忽略了水的浓度。然而,实验结果表明,料水比对 TOC 分解有显著影响。考虑到反应中的水浓度,采用非线性回归分析法(Runge-Kutta 法)计算了 TOC (2.35) 和水 (1.45) 的反应阶数。计算得出的预指数(k')和活化能(E)分别为 8.1 ± 2/min 和 90.37 ± 9.38 kJ/mol。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Kinetics study of total organic carbon destruction during supercritical water gasification of glucose

The kinetics of total organic carbon (TOC) destruction during supercritical water gasification (SCWG) of glucose were studied at 400–500°C and 25 MPa in a 600 mL batch reactor. Both TOC and water concentrations are critical for the conversion of TOC in supercritical water, especially at longer residence times. Initially, it was assumed that the TOC destruction reaction followed first-order kinetics ignoring the water concentration. However, experimental results showed that the feed-to-water ratio had a significant effect on TOC decomposition. Considering the water concentration in the reaction, the reaction orders of TOC (2.35) and water (1.45) were calculated using nonlinear regression analysis (the Runge-Kutta method). The estimated pre-exponential factor (k’) and activation energy (E) were calculated to be 8.1 ± 2/min and 90.37 ± 9.38 kJ/mol respectively.

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来源期刊
CiteScore
3.30
自引率
6.70%
发文量
74
审稿时长
3 months
期刊介绍: As the leading archival journal devoted exclusively to chemical kinetics, the International Journal of Chemical Kinetics publishes original research in gas phase, condensed phase, and polymer reaction kinetics, as well as biochemical and surface kinetics. The Journal seeks to be the primary archive for careful experimental measurements of reaction kinetics, in both simple and complex systems. The Journal also presents new developments in applied theoretical kinetics and publishes large kinetic models, and the algorithms and estimates used in these models. These include methods for handling the large reaction networks important in biochemistry, catalysis, and free radical chemistry. In addition, the Journal explores such topics as the quantitative relationships between molecular structure and chemical reactivity, organic/inorganic chemistry and reaction mechanisms, and the reactive chemistry at interfaces.
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