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Kinetic modelling and a novel packed bed photocatalytic reactor.

机译:动力学建模和新型填充床光催化反应器。

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A superior parameter estimation approach, based on the Box-Draper method of non-linear estimation using all the experimental data, is described and compared to the method of initial rates. It is shown that this approach results in better and more objective parameter estimates in the Langmuir-Hinshelwood kinetic models typically applicable to photocatalytic reactions.; The photocatalytic degradation of tetrahydrofuran, 1,4-dioxane, and their mixture is achieved in near-UV illuminated aqueous titanium dioxide slurries.; Two different commercial photocatalysts, Degussa P25 and Hombikat UV 100, are used to degrade 1,4-dioxane photocatalytically in an annular slurry photoreactor. The optimum photocatalyst loading for Degussa P25 is found to be 1.5 gL{dollar}sp{lcub}-1{rcub}{dollar} while for Hombikat UV 100, it is between 3.0-4.0 gL{dollar}sp{lcub}-1{rcub}{dollar}. The photoactivity of Degussa P25 is higher than Hombikat at lower concentrations whereas it is lower at higher concentrations. The photoactivity of UV 100 titanium dioxide is found to be twice that of Degussa P25 at optimum concentrations. Degussa P25 titanium dioxide with the optimum concentration of 1.5 gL{dollar}sp{lcub}-1{rcub}{dollar} is used in the kinetic studies of tetrahydrofuran, 1,4-dioxane, and their mixture.; Using both gas chromatography/mass spectrometry (GC/MS) and ion chromatography (IC) methods, possible intermediates for the photocatalytic degradation of tetrahydrofuran and 1,4-dioxane are identified. 2(3H)-Furan-one, dihydro-({dollar}gamma{dollar}-butyrolactone), succinic acid, acetic acid, formic acid, {dollar}beta{dollar}-hydroxybutyric acid, and glycolic acid are identified as tetrahydrofuran intermediates during its photocatalytic reaction. Similarly, 1,2-ethanediol, diformate, acetic acid, formic acid, {dollar}beta{dollar}-hydroxybutyric acid, and glycolic acid are identified as intermediates of the photocatalytic degradation of 1,4-dioxane.; Based on the proposed intermediates, reaction mechanism pathways and kinetic models for the photocatalytic degradation of tetrahydrofuran, 1,4-dioxane, and their mixture are developed. It is shown that the photocatalytic degradation of tetrahydrofuran and the binary system follows a modified Langmuir-Hinshelwood rate form whereas 1,4-dioxane follows a simple Langmuir-Hinshelwood model.; Finally, a novel tellerette packed bed photoreactor (TPBP) is introduced. Stainless steel is used to make the tellerette packings. The experiments reveal that mass transfer limitations in this packed bed photoreactor are insignificant, such that the reaction appears to be kinetically controlled. Also, it is shown that the ratio of the surface area of the photocatalyst to the photoreactor volume is adequate and sufficient UV light penetrates throughout the system.
机译:描述了一种基于使用所有实验数据进行非线性估计的Box-Draper方法的优越参数估计方法,并将其与初始速率方法进行了比较。结果表明,这种方法在通常适用于光催化反应的Langmuir-Hinshelwood动力学模型中产生了更好,更客观的参数估计。四氢呋喃,1,4-二恶烷及其混合物的光催化降解是在近紫外线照明的二氧化钛水溶液中完成的。两种不同的市售光催化剂Degussa P25和Hombikat UV 100用于在环形浆料光反应器中光催化降解1,4-二恶烷。发现Degussa P25的最佳光催化剂负载量为1.5 gL {dollar} sp {lcub} -1 {rcub} {dollar},而Hombikat UV 100则为3.0-4.0 gL {dollar} sp {lcub} -1 {rcub} {dollar}。在较低浓度下,Degussa P25的光活性高于Hombikat,而在较高浓度下则较低。发现在最佳浓度下,UV 100二氧化钛的光活性是Degussa P25的两倍。最佳浓度为1.5 gL {dol}} sp {lcub} -1 {rcub} {dol}的Degussa P25二氧化钛用于四氢呋喃,1,4-二恶烷及其混合物的动力学研究。使用气相色谱/质谱法(GC / MS)和离子色谱法(IC),可以鉴定出四氢呋喃和1,4-二恶烷的光催化降解中间体。 2(3H)-呋喃一,二氢-({美元}γ{美元}-丁内酯),琥珀酸,乙酸,甲酸,{美元}β{美元}-羟基丁酸和乙醇酸被鉴定为四氢呋喃在其光催化反应过程中的中间体。类似地,将1,2-乙二醇,二甲酸酯,乙酸,甲酸,{β} {USD}-羟基丁酸和乙醇酸鉴定为1,4-二恶烷的光催化降解的中间体。基于所提出的中间体,开发了光催化降解四氢呋喃,1,4-二恶烷及其混合物的反应机理途径和动力学模型。结果表明,四氢呋喃和二元体系的光催化降解遵循改良的Langmuir-Hinshelwood速率形式,而1,4-二恶烷遵循简单的Langmuir-Hinshelwood模型。最后,介绍了一种新颖的柜式床光反应器(TPBP)。不锈钢是用来做出纳员包装的。实验表明,在该填充床光反应器中传质限制是微不足道的,因此该反应似乎是动力学控制的。同样,显示出光催化剂的表面积与光反应器体积的比率是适当的,并且足够的UV光穿透整个系统。

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