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Biosorption of Pb (II) from aqueous solution by extracellular polymeric substances extracted from Klebsiella sp. J1: Adsorption behavior and mechanism assessment

机译:从Klebsiella sp。提取的细胞外聚合物对水溶液中Pb(II)的生物吸附。 J1:吸附行为和机理评估

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摘要

The adsorption performance and mechanism of extracellular polymeric substances (EPS) extracted from Klebsiella sp. J1 for soluble Pb (II) were investigated. The maximum biosorption capacity of EPS for Pb (II) was found to be 99.5 mg g−1 at pH 6.0 and EPS concentration of 0.2 g/L. The data for adsorption process satisfactorily fitted to both Langmuir isotherm and pseudo-second order kinetic model. The mean free energy E and activation energy Ea were determined at 8.22– 8.98 kJ mol−1 and 42.46 kJ mol−1, respectively. The liquid-film diffusion step might be the rate-limiting step. The thermodynamic parameters (ΔGo, ΔHo and ΔSo) revealed that the adsorption process was spontaneous and exothermic under natural conditions. The interactions between EPS system and Pb (II) ions were investigated by qualitative analysis methods (i.e Zeta potential, FT-IR and EDAX). Based on the strong experimental evidence from the mass balance of the related elements participating in the sorption process, an ion exchange process was identified quantitatively as the major mechanism responsible for Pb (II) adsorption by EPS. Molar equivalents of both K+ and Mg2+ could be exchanged with Pb2+ molar equivalents in the process and the contribution rate of ion exchange to adsorption accounted for 85.72% (Δmequiv = −0.000541).
机译:从克雷伯菌(Klebsiella sp。)提取的细胞外聚合物(EPS)的吸附性能和机理。研究了可溶性Pb(II)的J1。在pH 6.0和EPS浓度为0.2μg/ L的条件下,EPS对Pb(II)的最大生物吸附能力为99.5μgg-1。吸附过程的数据令人满意地拟合到Langmuir等温线和拟二级动力学模型。平均自由能E和活化能Ea分别确定为8.22–8.98 kJ mol-1和42.46 kJ mol-1。液膜扩散步骤可以是限速步骤。热力学参数(ΔGo,ΔHo和ΔSo)表明,吸附过程在自然条件下是自发的且放热的。通过定性分析方法(即Zeta电位,FT-IR和EDAX)研究了EPS体系与Pb(II)离子之间的相互作用。基于参与吸附过程中相关元素的质量平衡的有力实验证据,定量地确定了离子交换过程是EPS吸附Pb(II)的主要机理。摩尔当量的K +和Mg2 +可以与Pb2 +摩尔当量交换,离子交换对吸附的贡献率为85.72%(Δmequiv= -0.000541)。

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