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A fluidized-bed reactor for the photocatalytic mineralization of phenol on TiO2-coated silica gel

机译:流化床反应器用于TiO2涂层硅胶上苯酚的光催化矿化

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摘要

TiO2 photocatalysis represents a promising class of oxidation techniques that are intended to be both supplementary and complementary to the conventional approaches for the removal of refractory and trace organic contaminants in water and air. Powdered TiO2 dispersion systems employed in most studies require an additional separation step to recover the catalyst from the effluent water, which represents a major drawback for large scale applications. The optimization of photocatalytic treatment systems involves merging the benefits of catalyst immobilization on a retainable support, thus eliminating the need for downstream catalyst separation, maximization of photon-exposed catalyst area, and continuous operation.Aiming to integrate such conditions into a single system, a bench-scale annular photo-reactor with concentric UV-C lamp was built to study the photocatalytic mineralization of phenol on fluidized silica gel beads coated with sol-gel-synthetized TiO2. Reactor efficiency was investigated for different silica particle diameters (224, 357 and 461 μm), fluidized-bed concentrations in the bulk liquid (5, 10, 20 and 30 g L−1), initial phenol concentrations in the aqueous solution (0.25 mmol L−1 to 4.0 mmol L−1), and single and multiple sol-gel depositions. Then, the resulting optimum reactor configuration was compared to that of the same process on suspended Degussa P25 TiO2 nanoparticles under similar experimental conditions. The latter is expected to be more efficient, but post-treatment catalyst recovery, being an energy intensive process, represents a major limitation for large scale applications. Process efficiency was measured as a function of the accumulated energy necessary for the mineralization of 50% of the initial dissolved chemical oxygen demand (COD), or, Q0.5. Results showed that for any given mass of fluidized bed material, photo-oxidation efficiency increases with decreasing particle size (even for bed concentrations with similar equivalent surface area), decreasing initial phenol concentrations, and increasing number of sol-gel coatings. It was found that, for any given particle size and contaminant mass, there is an optimum bed concentration of 20 g L−1 for which Q0.5 reaches a minimum. Finally, under the optimum configuration, the fluidized-bed reactor efficiency is only 30% lower than that of photocatalysis on suspended TiO2 nanopowder, thus making the proposed fluidized system a viable alternative to slurry-TiO2 reactors.
机译:TiO2光催化代表了有前途的一类氧化技术,旨在作为传统方法的补充和补充,以去除水和空气中的难处理和痕量有机污染物。大多数研究中使用的粉状TiO2分散系统需要额外的分离步骤以从废水中回收催化剂,这对于大规模应用而言是一个主要缺点。光催化处理系统的优化涉及将催化剂固定在可保留载体上的好处合并在一起,从而消除了下游催化剂​​分离,光子暴露的催化剂面积最大化和连续运行的需求。建立了带同心UV-C灯的台式环形光反应器,研究了溶胶-凝胶合成的TiO2包覆的流化硅胶珠上苯酚的光催化矿化作用。研究了不同二氧化硅粒径(224、357和461μm),散装液体中流化床浓度(5、10、20和30 g L -1 ),初始苯酚浓度的反应器效率在水溶液中(0.25 mmol L -1 到4.0 mmol L -1 ),以及一次和多次溶胶-凝胶沉积。然后,在相似的实验条件下,将得到的最佳反应器配置与悬浮Degussa P25 TiO2纳米颗粒上的相同过程进行了比较。预期后者将更有效,但是后处理催化剂的回收是一种能源密集型方法,对大规模应用而言是主要的限制。测量过程效率是矿化初始溶解化学需氧量(COD)的50%或Q0.5所需的累积能量的函数。结果表明,对于任何给定质量的流化床材料,光氧化效率都会随着粒径的减小而增加(即使对于具有相似等效表面积的床浓度而言),初始酚浓度降低和溶胶-凝胶涂层数量也会增加。结果发现,对于任何给定的粒径和污染物质量,最佳床层浓度均为20 g L -1 ,其中Q0.5达到最小值。最后,在最佳配置下,流化床反应器的效率仅比悬浮的TiO2纳米粉的光催化效率低30%,因此使拟议的流化系统成为浆体TiO2反应器的可行替代方案。

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