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Kinetic study of the photo-Fenton degradation of formic acid Combined effects of temperature and iron concentration

机译:光芬宁甲酸综合影响的光芬顿劣化的动力学研究

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摘要

This study is focused on the kinetic modelling of the Fenton and photo-Fenton degradation of a model pollutant (formic acid) in aqueous solution, for relatively low iron concentrations (1-9 ppm). The reaction rate expressions are derived from an accepted reaction mechanism and explicitly having into account the local volumetric rate of photon absorption. The experimental work was performed in a well-stirred tank laboratory reactor irradiated from the bottom. Afterward, the proposed kinetic model and the experimental data were used to estimate the Arrhenius parameters between 20 and 55 °C, applying a non-linear regression procedure. To avoid the precipitation of iron compounds during the experimental runs, simultaneous high reaction temperatures (55 °C) and iron concentrations (9 ppm) were prevented. To achieve this goal, an experimental design based on the D-optimality criterion was adopted. The proposed kinetic model was able to reproduce the combined effects of changing the ferric iron concentrations, reaction temperatures, and formic acid to hydrogen peroxide molar ratios on the pollutant degradation rate. Kinetic model predictions are compared with experimental data of the organic compound conversion, and a good agreement is obtained. For the whole set of Fenton and photo-Fenton experimental runs, the maximum root mean square error is 7.64%.
机译:本研究专注于芬顿和光芬顿在水溶液中污染物(甲酸)的芬顿和光芬顿降解的动力学建模,用于相对低的铁浓度(1-9ppm)。反应速率表达衍生自接受的反应机制,并明确考虑到光子吸收的局部体积速率。实验工作在从底部照射的搅拌罐实验室反应器中进行。之后,所提出的动力学模型和实验数据用于估计20至55°C之间的Arrhenius参数,应用非线性回归过程。为了避免在实验过程中沉淀铁化合物,预防同时高反应温度(55℃)和铁浓度(9ppm)。为实现这一目标,采用了一种基于D-Optimaly标准的实验设计。所提出的动力学模型能够再现改变铁浓度,反应温度和甲酸对过氧化氢摩尔比的组合效果,以污染物降解率。与有机化合物转化的实验数据进行比较动力学模型预测,并获得了良好的一致性。对于整套FENTON和PHOGON-FENTON实验运行,最大根均方误差为7.64%。

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