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The interaction mechanism of Th(IV) on sepiolite investigated by batch and modeling techniques

机译:批料和建模技术研究Th(IV)在海泡石上的相互作用机理

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The effect of Paecitomyces cateniannulatus (P. cateniannulatus) on Th(IV) adsorption by sepiolite were investigated by batch techniques. The batch adsorption showed that the adsorption of Th(IV) on sepiolite and sepiolite + P. catenlannulatus significantly increased with increasing of pH from 3.0 to 6.0, then remained the high-level adsorption. P. cateniannulatus significantly facilitated the adsorption of Th(IV) on sepiolite at pH 2.0-5.0, whereas inhibited adsorption was observed at pH > 6.0. The adsorption of Th(IV) on sepiolite + P. catenlannulatus was independent of ionic strength at pH from 3.0 to 9.0. The adsorption kinetics of Th(IV) on sepiolite and sepiolite + P. catenlannulatus can be satisfactorily simulated by pseudo-second-order kinetic model. The maximum adsorption capacities of sepiolite and sepiolite + P. catenlannulatus for Th(IV) calculated Langmuir model at pH 3.0 and 293 K were 50.76 and 57.80 mg/g, respectively. Based on surface complexation modeling, the adsorption mechanism of Th(IV) on sepiocite + P. catenlannulatus was cation exchange/outer-sphere surface complexation at low pH, whereas inner-sphere surface complexation dominated the Th(IV) adsorption at high pH conditions. The findings presented in this study are of great importance towards understanding of fate and transport of heavy metals under natural aquatic environments. (C) 2016 Elsevier B.V. All tights reserved.
机译:通过分批技术研究了Paecitomyces cateniannulatus(P. cateniannulatus)对海泡石对Th(IV)吸附的影响。分批吸附表明,Th(IV)在海泡石和海泡石+链状假单胞菌上的吸附随着pH从3.0升高到6.0显着增加,然后保持高水平吸附。 P. cateniannulatus在pH 2.0-5.0时显着促进海泡石上Th(IV)的吸附,而在pH> 6.0时观察到抑制的吸附。 Th(IV)在海泡石+悬链假单胞菌上的吸附与pH值从3.0到9.0的离子强度无关。 Th(IV)在海泡石和海泡石+链状假单胞菌上的吸附动力学可以通过拟二级动力学模型令人满意地模拟。在pH 3.0和293 K下,海泡石和海泡石+链状假单胞菌对Th(IV)计算的Langmuir模型的最大吸附容量分别为50.76和57.80 mg / g。根据表面络合模型,在低pH值下,海泡石+链状假单胞菌对Th(IV)的吸附机理为阳离子交换/外球表面的络合,而在高pH条件下,内球表面的络合占Th(IV)的吸附为主。这项研究中提出的发现对了解自然水生环境中重金属的命运和运输具有重要意义。 (C)2016 Elsevier B.V.版权所有。

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