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本文引用的文献

1
Complex resistivity signatures of ethanol in sand-clay mixtures.乙醇在砂-粘土混合物中的复电阻率特征。
J Contam Hydrol. 2013 Jun;149:76-87. doi: 10.1016/j.jconhyd.2013.03.005. Epub 2013 Mar 29.
2
Aerobic biodegradation of iso-butanol and ethanol and their relative effects on BTEX biodegradation in aquifer materials.好氧条件下异丁醇和乙醇的生物降解及其对含水层中苯系物(BTEX)生物降解的相对影响。
Chemosphere. 2010 Nov;81(9):1104-10. doi: 10.1016/j.chemosphere.2010.09.003. Epub 2010 Sep 26.
3
Comparing the effects of various fuel alcohols on the natural attenuation of benzene plumes using a general substrate interaction model.采用通用基质相互作用模型比较各种燃料酒精对苯羽流自然衰减的影响。
J Contam Hydrol. 2010 Apr 1;113(1-4):66-76. doi: 10.1016/j.jconhyd.2010.02.002. Epub 2010 Feb 6.
4
Effect of ethanol and methyl-tert-butyl ether on monoaromatic hydrocarbon biodegradation: response variability for different aquifer materials under various electron-accepting conditions.乙醇和甲基叔丁基醚对单环芳烃生物降解的影响:不同电子受体条件下不同含水层物质的响应变异性
Environ Toxicol Chem. 2002 Dec;21(12):2631-9.
5
Effect of ethanol on BTEX biodegradation kinetics: aerobic continuous culture experiments.
Water Res. 2002 Sep;36(15):3739-46. doi: 10.1016/s0043-1354(02)00090-8.
6
Will ethanol-blended gasoline affect groundwater quality?
Environ Sci Technol. 2001 Jan 1;35(1):24A, 26A-30A. doi: 10.1021/es012247h.
7
Surface geochemistry of the clay minerals.黏土矿物的表面地球化学
Proc Natl Acad Sci U S A. 1999 Mar 30;96(7):3358-64. doi: 10.1073/pnas.96.7.3358.

不同乙醇浓度下砂-粘土混合物的比极化率

Specific polarizability of sand-clay mixtures with varying ethanol concentration.

作者信息

Sharma Sundeep, Slater Lee, Ntarlagiannis Dimitrios, Werkema Dale, Szabo Zoltan

机构信息

Department of Earth and Environmental Sciences, Rutgers University-Newark, Newark, NJ 07102, USA.

Environmental Chemistry Branch, Exposure Methods and Measurement Division, National Exposure Research Laboratory, Office of Research and Development, US Environmental Protection Agency, Las Vegas, NV 89119, USA.

出版信息

Near Surf Geophys. 2017 Dec;15(6):615-624. doi: 10.3997/1873-0604.2017049.

DOI:10.3997/1873-0604.2017049
PMID:35299702
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8925411/
Abstract

We utilise a concept of specific polarizability ( ), represented as the ratio of mineral-fluid interface polarization per pore-normalised surface area , 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 ( ). Specific polarizability estimates from previous complex conductivity measurements for bentonite-sand mixtures were compared with our dataset. The for all sand-clay mixtures decreased as the EtOH concentration increased from 0% to 10% to 20% v/v. We observe similar responses to EtOH concentration for all sand-clay mixtures. Analysis of variance with a level of significance = 0.05 suggests that the suppression in 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 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.

摘要

我们采用了比极化率( )的概念,其表示为每孔隙归一化表面积的矿物 - 流体界面极化率之比 ,以证明黏土 - 有机相互作用对复电导率测量的影响。对高岭石和伊利石 - 砂混合物进行了复电导率测量,测量结果是乙醇(EtOH)浓度(10%和20% v/v)变化的函数。每种黏土类型和渥太华砂的比表面积通过氮气吸附布鲁诺尔 - 埃米特 - 特勒方法测定。我们还根据干燥样品的重量损失计算了每种混合物的孔隙率和饱和度。将德拜分解(一种唯象模型)应用于复电导率数据,以确定归一化充电率( )。将之前膨润土 - 砂混合物复电导率测量得到的比极化率估计值与我们的数据集进行了比较。随着EtOH浓度从0%增加到10%再到20% v/v,所有砂 - 黏土混合物的 均降低。我们观察到所有砂 - 黏土混合物对EtOH浓度有相似的 响应。显著性水平 = 0.05的方差分析表明,对于所有砂 - 黏土混合物,随着EtOH浓度增加, 响应的抑制在统计上是显著的。另一方面,随着EtOH浓度增加,实电导率仅显示10%至20% v/v的变化。 估计值反映了复电导率测量对不同黏土类型在可用表面吸附位点处表面化学变化的敏感性,这可能是由黏土表面的离子交换引起的,并与黏土 - 水 - EtOH介质的双电层中的动力学反应有关。我们的结果表明,相对于黏土矿物学的变化,比表面积和乙醇浓度对黏土驱动的极化影响要大得多。