Impact of natural organic matter properties on the kinetics of suspended ion exchange process

被引:45
作者
Bazri, Mohammad Mahdi [1 ]
Mohseni, Madjid [1 ]
机构
[1] Univ British Columbia, Dept Chem & Biol Engn, Vancouver, BC V5Z 1M9, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Ion exchange; Adsorption; Diffusion; Natural organic matter; Molecular diffusivity; FIELD-FLOW FRACTIONATION; FLUORESCENCE CORRELATION SPECTROSCOPY; RIVER FULVIC-ACID; ANION-EXCHANGE; ACTIVATED CARBON; DIFFUSION-COEFFICIENTS; PROTEIN ADSORPTION; HUMIC SUBSTANCES; MOLECULAR-WEIGHT; NOM FRACTIONS;
D O I
10.1016/j.watres.2015.12.036
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Removal kinetics of four standard organic matter isolates under the application of strongly basic ion exchange resins (IEX) in suspended mode was studied under commercial application conditions. Suwannee River natural organic matter (SRNOM), SR fulvic acid (SRFA), and Pony Lake fulvic acid (PLFA) were greatly removed (>90%) and highly preferred by IEX resins (alpha > 5, over Cl-, and HCO3-) while SR humic acid (SRHA) was the least preferred organic structure among the four isolates studied (alpha approximate to 1). Moreover, the efficacy of removal for fulvic acids (i.e., SRFA, PLFA) was consistent over consecutive reuse of IEX resins (i.e., loading cycles) whereas it decreased for SRNOM and SRHA over the course of operation. The stoichiometric correlation between the chloride released from the resins as a result of organic molecules uptake indicated that ion exchange was the dominant mechanism. Results obtained indicated that molecular weight and charge density of isolates played a major role in the performance of ion exchange process for organic matter removal. Furthermore, various empirical and physical models were evaluated using the experimental data and pore diffusion was found to be the rate-liming step during the uptake of organic matters; hence, it was used as the appropriate model to predict the kinetics of removal. Consequently, free liquid diffusivities and effective pore diffusion coefficients of organic molecules were estimated and findings were in agreement with the literature data that were obtained from spectrophotometric methods. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:147 / 155
页数:9
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