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Kinetic and mass transfer studies of ozone degradation of organics in liquid/gas-ozone and liquid/solid-ozone systems.

机译:在液/气-臭氧和液/固-臭氧系统中有机物的臭氧降解的动力学和传质研究。

摘要

This work was concerned with the determination of mass transfer and kinetic parameters of ozone reactions with four organic compounds from different families, namely reactive dye RO16, triclocarban, naphthalene and methanol. In order to understand the mechanisms of ozone reactions with the organic pollutants, a radical scavenger (t-butanol) was used and the pH was varied from 2 to 9.udOzone solubility (CAL*) is an important parameter that affects both mass transfer rates and chemical reaction kinetics. In order to determine accurate values of the CAL* in the current work, a set of experiments were devised and a correlation between CAL* and the gas phase ozone concentration of the form CAL*(mol/L) = 0.0456 CO3 (g/m3 NTP) was obtained at 20°C. This work has also revealed that t-butanol did not only inhibit hydroxyl radical reactions but also increased mass transfer due to it increasing the specific surface area (aL). Values of the aL were determined to be 2.7 and 3.5 m2/m3 in the absence and presence of t-butanol respectively. It was noticed that the volumetric mass transfer coefficient (kLa) has increased following the addition of t-butanol.udOzone decomposition was studied at pH values of 2 to 9 in a 500 mL reactor initially saturated with ozone. Ozone decomposition was found to follow a second order reaction at pH values less than 7 whilst it was first order at pH 9. When the t-butanol was added, the decomposition of ozone progressed at a lower reaction order of 1.5 for pH values less than 7 and at the same order without t-butanol at pH 9. Ozone decomposition was found significant at high pHs due to high hydroxide ion concentration, which promotes ozone decomposition at high pHs.udThe reaction rate constant (k) of RO16 ozonation in the absence of t-butanol was determined. The result suggests that RO16 degradation occurs solely by molecular ozone and indirect reactions by radicals are insignificant.udThe chemical reaction of triclocarban with ozone was found to follow second order reaction kinetics. The degradation of naphthalene using the liquid/gas-ozone (LGO) system was studied. This result showed that hydroxyl radicals seemed to have limited effect on naphthalene degradation which was also observed when a radical scavenger (t-butanol) was used. Reaction rate constants were calculated and were found around 100 times higher than values reported in the literature due to differences in experimental conditions. From the results of the experimental investigation on the degradation of methanol by ozone it was found that the rate constant (k) of the degradation reaction increased at pH 9. The reaction stoichiometry was found to have a value of 1 mol/mol.udThe two steps of the liquid/solid-ozone (LSO) system were studied on beds of silica gel and a zeolitic material (D915) and the ozone adsorption process was modeled and found that particle rate controls ozone adsorption step but liquid rate controls the water treatment step.udOzone desorption with pure deionised water was studied. The water flow rate was found to accelerate the desorption rates but pH was found to decrease the desorption rates. In contrast, the effect of pH was insignificant in the presence of t-butanol.udDetermination of the adsorption isotherms for RO16, naphthalene and methanol revealed that RO16 did not exhibit adsorption on silica gel, but both naphthalene and methanol showed adsorption on D915 described by Langmuir model.
机译:这项工作涉及测定来自不同家族的四种有机化合物(即活性染料RO16,三氯卡班,萘和甲醇)的臭氧反应的传质和动力学参数。为了了解臭氧与有机污染物反应的机理,使用了自由基清除剂(叔丁醇),pH值在2到9之间变化。ud臭氧溶解度(CAL *)是影响两种传质的重要参数速率和化学反应动力学。为了确定当前工作中CAL *的准确值,设计了一组实验,CAL *与CAL *(mol / L)= 0.0456 CO3(g / m3)形式的气相臭氧浓度之间的相关性NTP)在20°C下获得。这项工作还表明,叔丁醇不仅抑制羟基自由基反应,而且由于其增加了比表面积(aL)而增加了质量转移。在不存在和存在叔丁醇的情况下,aL的值分别确定为2.7和3.5 m2 / m3。注意到在添加叔丁醇之后,体积传质系数(kLa)增加了。在最初用臭氧饱和的500 mL反应器中,在pH值为2至9的条件下研究了臭氧分解。发现臭氧分解在pH值小于7时发生二级反应,而在pH 9时发生一级反应。当添加叔丁醇时,pH值小于5时,臭氧的分解反应以较低的1.5级进行。 7和在pH 9下没有叔丁醇的相同顺序。由于高氢氧根离子浓度,在高pH下发现臭氧分解很明显,这会在高pH值下促进臭氧分解。确定不存在叔丁醇。结果表明,RO16的降解仅通过分子臭氧发生,而自由基的间接反应则微不足道。 ud三氯卡班与臭氧的化学反应遵循二级反应动力学。研究了使用液/气-臭氧(LGO)系统降解萘。该结果表明羟基自由基似乎对萘降解具有有限的作用,当使用自由基清除剂(叔丁醇)时也观察到。计算了反应速率常数,由于实验条件的差异,发现其反应速率常数比文献报道的值高约100倍。从有关臭氧降解甲醇的实验研究结果中发现,降解反应的速率常数(k)在pH 9时增加。反应化学计量为1 mol / mol。在硅胶和沸石材料(D915)上研究了液/固臭氧(LSO)系统的两个步骤,并对臭氧吸附过程进行了建模,发现颗粒率控制着臭氧吸附步骤,而液率控制着水处理用纯去离子水对臭氧进行了脱附研究。发现水流速加速了解吸速率,但是发现pH降低了解吸速率。相反,在叔丁醇存在下,pH的影响不明显。 ud对RO16,萘和甲醇的吸附等温线的测定表明,RO16在硅胶上没有吸附,但是萘和甲醇在D915上均显示了吸附。由Langmuir模型。

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    Grima N. M. M.;

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  • 年度 2009
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  • 正文语种 en
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