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Specific polarizability of sand-clay mixtures with varying ethanol concentration

机译:具有不同乙醇浓度的砂粘土混合物的比极化性

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摘要

We utilise a concept of specific polarizability (c(s)), represented as the ratio of mineral-fluid interface polarization per pore-normalised surface area S-p, to demonstrate the influence of clay-organic interaction on complex conductivity measurements. Complex conductivity measurements were performed on kaolinite-and illite-sand mixtures as a function of varying ethanol (EtOH) concentration (10% and 20% v/v). The specific surface area of each clay type and Ottawa sand was determined by nitrogen-gas-adsorption Brunauer-Emmett-Teller method. We also calculated the porosity and saturation of each mixture based on weight loss of dried samples. Debye decomposition, a phenomenological model, was applied to the complex conductivity data to determine normalised chargeability (m(n)). Specific polarizability estimates from previous complex conductivity measurements for bentonite-sand mixtures were compared with our dataset. The c(s) for all sand-clay mixtures decreased as the EtOH concentration increased from 0% to 10% to 20% v/v. We observe similar c(s) responses to EtOH concentration for all sand-clay mixtures. Analysis of variance with a level of significance alpha = 0.05 suggests that the suppression in c(s) responses with increasing EtOH concentration was statistically significant for all sand-clay mixtures. On the other hand, real conductivity showed only 10% to 20% v/v changes with increasing EtOH concentration. The c(s) estimates reflect the sensitivity of complex conductivity measurements to alteration in surface chemistry at available surface adsorption sites for different clay types, likely resulting from ion exchange at the clay surface and associated with kinetic reactions in the electrical double layer of the clay-water-EtOH media. Our results indicate a much larger influence of specific surface area and ethanol concentration on clay-driven polarization relative to changes in clay mineralogy.
机译:我们利用特定极化性(C(S))的概念,表示为每孔归一化表面积S-P的矿物流体界面偏振的比率,以证明粘土 - 有机相互作用对复杂电导率测量的影响。在高岭石和illite-砂混合物上进行复杂的电导率测量,作为不同乙醇(EtOH)浓度(10%和20%v / v)的函数。通过氮气吸附Brunauer-Emmett-Teller方法测定每个粘土型和渥太华砂的比表面积。我们还基于干燥样品的重量损失计算每个混合物的孔隙率和饱和度。德义分解,一种现象学模型被应用于复杂的电导率数据以确定归一化的充电能力(M(n))。与我们的数据集进行比较来自先前复杂电导率测量的特定极化性估计。当EtOH浓度增加到0%至10%至20%v / v时,所有砂粘土混合物的C(S)降低。我们观察到所有砂粘土混合物的EtOH浓度的类似C. α= 0.05水平的差异分析表明,对于所有砂粘土混合物,C(S)反应中的抑制性均显着显着。另一方面,实际电导率仅显示10%至20%V / V随着EtOH浓度的增加而变化。 C(S)估计反映了复杂电导率测量对不同粘土类型的可用表面吸附位点的表面化学改变的敏感性,可能由粘土表面的离子交换产生并与粘土的电双层中的动力学反应相关-water-etoh培养基。我们的结果表明,特定表面积和乙醇浓度相对于粘土矿物的变化对粘土驱动偏振的影响更大。

著录项

  • 来源
    《Near surface geophysics》 |2017年第6期|共10页
  • 作者单位

    Rutgers Univ Newark Dept Earth &

    Environm Sci Newark NJ 07102 USA;

    Rutgers Univ Newark Dept Earth &

    Environm Sci Newark NJ 07102 USA;

    Rutgers Univ Newark Dept Earth &

    Environm Sci Newark NJ 07102 USA;

    US EPA Environm Chem Branch Exposure Methods &

    Measurement Div Natl Exposure Res Lab Off Res &

    Dev Las Vegas NV 89119 USA;

    US Geol Survey New Jersey Water Sci Ctr Lawrenceville NJ 08648 USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 地球物理学;
  • 关键词

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