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Integrated investigations on the adsorption mechanisms of fulvic and humic acids on three clay minerals

机译:腐殖酸和腐殖酸在三种黏土矿物上的吸附机理的综合研究

摘要

Adsorption behaviors of fulvic acid (FA) and humic acid (HA) on kaolinite, smectite and vermiculite were investigated. To explore the adsorption mechanism, characterization of both the adsorption FA/HA-clay complexes and suspensions was conducted by utilizing multiple analytical techniques including liquidstate H-1 nuclear magnetic resonance spectroscopy, high performance size exclusion chromatography, UV-vis spectroscopy, Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. Both FA and HA underwent fractionation during the adsorption due to different affinity for the functional moieties of FA/HA on the minerals. More HA was adsorbed than FA on kaolinite and smectite mainly via hydrophobic interaction. Electron transfer from aromatic units of FA to iron cation induced more FA than HA adsorbed onto vermiculite at higher FA/HA concentrations (>20 mg C/L). Specific surface area and pore volume analyses indicated HA with larger particle size was prone to accumulate on the external mineral surfaces, while FA was easier than HA to block pores of the minerals. The increased pH in clay suspensions after FA/HA adsorption suggested that ligand exchange occurred and FA/HA-clay complexes formed, particularly for the 2:1 type minerals of smectite and vermiculite with the increase of pH at 0.41 and 0.62 units, respectively. Furthermore, the increase of the equilibrium pH or the decrease of the ionic strength led to the reduction of FA/HA adsorption on all the three minerals. Due to rich in iron cation, more carboxyl and hydroxyl functional groups were facilitated for the ligand exchange and cation-bridging on vermiculite, and thus improved the adsorption capacity. The results of this study will improve our understanding of the roles of mineral interfacial properties, characteristics of FA and HA in the adsorption of FA/HA on clay minerals. (C) 2012 Elsevier B.V. All rights reserved.
机译:研究了黄腐酸(FA)和腐殖酸(HA)在高岭石,蒙脱石和ver石上的吸附行为。为了探索吸附机理,利用多种分析技术对FA / HA-粘土复合物和悬浮液进行了表征,包括液相H-1核磁共振波谱,高性能尺寸排阻色谱,紫外可见光谱,傅里叶变换红外光谱光谱和X射线光电子能谱。由于对矿物质中FA / HA的功能部分具有不同的亲和力,因此FA和HA都在吸附过程中经历了分馏。高岭土和蒙脱石上的HA吸附量比FA高,主要是通过疏水作用。在较高的FA / HA浓度(> 20 mg C / L)下,电子从FA的芳族单元转移到铁阳离子时,所吸附的FA比HA吸附到ver石上的HA多。比表面积和孔体积分析表明,具有较大粒径的HA易于在矿物外部表面积聚,而FA比HA更容易堵塞矿物的孔。 FA / HA吸附后粘土悬浮液的pH升高表明发生了配体交换并形成了FA / HA-粘土络合物,尤其是对于蒙脱石和ver石的2:1型矿物,pH分别升高了0.41和0.62个单位。此外,平衡pH的增加或离子强度的降低导致FA / HA在所有三种矿物上的吸附减少。由于富含铁阳离子,更多的羧基和羟基官能团有助于for石上的配体交换和阳离子桥联,从而提高了吸附能力。这项研究的结果将增进我们对矿物界面性质,FA和HA特性在粘土矿物上吸附FA / HA的作用的理解。 (C)2012 Elsevier B.V.保留所有权利。

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