Factors affecting selectivity during dissolved organic matter removal by anion-exchange resins

2007 ◽  
Vol 41 (18) ◽  
pp. 4211-4221 ◽  
Author(s):  
Yongrui Tan ◽  
James E. Kilduff
2012 ◽  
Vol 12 (5) ◽  
pp. 630-636 ◽  
Author(s):  
A. Phetrak ◽  
J. Lohwacharin ◽  
N. Watanabe ◽  
M. Murakami ◽  
H. Sakai ◽  
...  

Four strong-base anion exchange resins (AERs) with different properties were selected to investigate dissolved organic matter (DOM) removal from river water containing inorganic anions. Rapid sand-filtered water was obtained from a water treatment plant in Tokyo, Japan, and then concentrated by an ultrafiltration membrane for use in ion exchange experiments to simulate high dissolved organic carbon (DOC) and sulfate conditions. AERs removed 23–50% of DOC and 70–80% of UV254 within 30 min despite high sulfate concentration (121 mg/L). Although the materials and structure of the AERs did not affect the reduction of UV254, DOC removal was affected. The highest DOC reduction was achieved by a macroporous polyacrylic AER (Purolite), while the macroporous polystyrene IRA 910 had the lowest DOC removal. A pseudo-second-order kinetic model showed that the rate constants and the initial sorption rates of polyacrylic resins were higher than those by polystyrene resins, suggesting that more hydrophilic structure of AERs exhibited faster DOC removal. Aromatic DOM with a molecular weight (MW) of 800–3,000 Da was almost completely removed by AERs, whereas only half of aromatic DOMs smaller than 800 Da were removed by AERs. Adsorbed DOC comprised less than 6% of all exchanged anions, whereas the adsorbed sulfate was about 90% due to comparatively high concentration of sulfate in the water sample.


2014 ◽  
Vol 14 (4) ◽  
pp. 577-584 ◽  
Author(s):  
Elizabeth A. Crafton ◽  
Danyang Wu ◽  
Stephen E. Duirk

Anion exchange resins (AERs) were compared with aluminum-based coagulants for reducing disinfection by-product (DBP) precursor concentrations from a source water collected in northeast Ohio, USA. Three AERs (IRA-910, IRA-958, and MIEX) were evaluated to determine which resin would remove the most natural organic matter (NOM) and moieties responsible for DBP formation. All the AERs were found to be highly proficient at NOM removal specifically the moieties that absorb UV254 (i.e., chromophores) over 75 min of contact time; however, MIEX removed NOM at a faster rate than IRA-910 and IRA-958 resins. Enhanced coagulation was effective at removing approximately 35% of the NOM and 40–60% of the chromophores and fluorophores (i.e., excitation–emission matrix pairs A and C). DBP formation was determined as a function of pH for the different NOM removal processes. MIEX treatment resulted in significant reduction in DBP concentrations when compared to chlorinating the raw source water. MIEX generally out-performed enhanced coagulation for reducing DBP formation. However, alum was found to remove more NOM and resulted in less DBPs compared to aluminum chlorohydrate. This could impact water utilities trying to balance the health effects due to DBP exposure verses chemical/sludge management costs.


1999 ◽  
Vol 40 (9) ◽  
pp. 207-214 ◽  
Author(s):  
J.-P. Croué ◽  
D. Violleau ◽  
C. Bodaire ◽  
B. Legube

The objective of this work was to compare the affinity of well characterized NOM fractions isolated from two surface waters with strong (gel matrix and macroporous matrix) and weak anion exchange resins (AER) using batch experiment conditions. The structural characterization of the fraction of NOM has shown that the higher the hydrophilic character, the lower the C/O atomic ratio, the lower the SUVA, the lower the aromatic carbon content and the lower the molecular weight. In general (not always), strong AER was more efficient to remove DOC than weak AER. For the same water source (Suwannee River), the higher the molecular weight of the NOM fraction, the lower the affinity with AER. Increasing the ionic strength favored the removal of the hydrophobic NOM fraction (“salting out” effect) while increasing the pH apparently reduced the removal of the hydrophilic NOM fraction. Results were discussed in terms of size exclusion, adsorption, anion exchange and also hydrophobic/hydrophilic repulsion.


2020 ◽  
pp. 039139882094773
Author(s):  
Karin Strobl ◽  
Stephan Harm ◽  
Ute Fichtinger ◽  
Claudia Schildböck ◽  
Jens Hartmann

Introduction: Heparin and citrate are commonly used anticoagulants in membrane/adsorption based extracorporeal liver support systems. However, anion exchange resins employed for the removal of negatively charged target molecules including bilirubin may also deplete these anticoagulants due to their negative charge. The aim of this study was to evaluate the adsorption of citrate by anion exchange resins and the impact on extracorporeal Ca2+ concentrations. Methods: Liver support treatments were simulated in vitro. Citrate and Ca2+ concentrations were measured pre and post albumin filter as well as pre and post adsorbents. In addition, batch experiments were performed to quantify citrate adsorption. Results: Pre albumin filter target Ca2+ concentrations were reached well with only minor deviations. Citrate was adsorbed by anion exchange resins, resulting in a higher Ca2+ concentration downstream of the adsorbent cartridges during the first hour of treatment. Conclusions: The anion exchange resin depletes citrate, leading to an increased Ca2+ concentration in the extracorporeal circuit, which may cause an increased risk of clotting during the first hour of treatment. An increase of citrate infusion during the first hour of treatment should therefore be considered to compensate for the adsorption of citrate.


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