scholarly journals Nanofiltration of perfluorooctanoic acid and perfluorooctane sulfonic acid as a function of water matrix properties

2019 ◽  
Vol 19 (8) ◽  
pp. 2199-2205
Author(s):  
Hadi Toure ◽  
A. H. M. Anwar Sadmani

Abstract Nanofiltration (NF) is a promising technology to remove the perfluoroalkyl acids, perfluorooctanoic acid (PFOA) and perfluorooctane sulfonic acid (PFOS) from water; however, little information is available as to how the natural water matrices impact PFOA and PFOS rejection when using NF. This study investigated the removal of PFOA and PFOS in laboratory-prepared water, surface water, and groundwater via NF to determine the effect of water matrix properties on PFOA and PFOS rejection by NF. PFOA and PFOS rejections were up to approximately 38% higher in the natural water matrices when compared to the laboratory-prepared water. The rejection of PFOA did not vary in the tested river water and groundwater; however, an increasing trend in PFOS rejection was observed and attributed to enhanced size exclusion of PFOS-cation complexes via the sulfonate (–SO3−) ‘head’ of the PFOS ions and cation-induced membrane fouling by natural organic matter. Compound rejection increased with declining flux that was consistent with the dissolved organic matter (DOM) content of the respective water matrices. This study confirmed that DOM and cations indigenous to natural water matrices can lead to improved rejection of PFOA and PFOS when using NF.

2014 ◽  
Vol 2014 ◽  
pp. 1-11 ◽  
Author(s):  
Vedat Uyak ◽  
Muge Akdagli ◽  
Mehmet Cakmakci ◽  
Ismail Koyuncu

The objective of this study was to investigate powdered activated carbon (PAC) contribution to natural organic matter (NOM) removal by a submerged MF and UF hybrid systems. It was found that filtration of surface waters by a bare MF and UF membranes removed negligible TOC; by contrast, significant amounts of TOC were removed when daily added PAC particles were predeposited on the membrane surfaces. These results support the assumption that the membranes surface properties and PAC layer structure might have considerably influential factor on NOM removal. Moreover, it was concluded that the dominant removal mechanism of hybrid membrane system is adsorption of NOM within PAC layer rather than size exclusion of NOM by both of membrane pores. Transmembrane pressure (TMP) increases with PAC membrane systems support the view that PAC adsorption pretreatment will not prevent the development of membrane pressure; on the contrary, PAC particles themselves caused membrane fouling by blocking the entrance of pores of MF and UF membranes. Although all three source waters have similar HPI content, it appears that the PAC interaction with the entrance of membrane pores was responsible for offsetting the NOM fractional effects on membrane fouling for these source waters.


2004 ◽  
Vol 4 (5-6) ◽  
pp. 215-222 ◽  
Author(s):  
A.R. Costa ◽  
M.N. de Pinho

Membrane fouling by natural organic matter (NOM), namely by humic substances (HS), is a major problem in water treatment for drinking water production using membrane processes. Membrane fouling is dependent on membrane morphology like pore size and on water characteristics namely NOM nature. This work addresses the evaluation of the efficiency of ultrafiltration (UF) and Coagulation/Flocculation/UF performance in terms of permeation fluxes and HS removal, of the water from Tagus River (Valada). The operation of coagulation with chitosan was evaluated as a pretreatment for minimization of membrane fouling. UF experiments were carried out in flat cells of 13.2×10−4 m2 of membrane surface area and at transmembrane pressures from 1 to 4 bar. Five cellulose acetate membranes were laboratory made to cover a wide range of molecular weight cut-off (MWCO): 2,300, 11,000, 28,000, 60,000 and 75,000 Da. Severe fouling is observed for the membranes with the highest cut-off. In the permeation experiments of raw water, coagulation prior to membrane filtration led to a significant improvement of the permeation performance of the membranes with the highest MWCO due to the particles and colloidal matter removal.


2002 ◽  
Vol 2 (5-6) ◽  
pp. 427-433 ◽  
Author(s):  
J. van Leeuwen ◽  
C. Chow ◽  
R. Fabris ◽  
N. Withers ◽  
D. Page ◽  
...  

To gain an improved understanding of the types of organic compounds that are recalcitrant to water treatment, natural organic matter (NOM) isolates from two drinking water sources (Mt. Zero and Moorabool reservoirs, Victoria, Australia) were separated into fractions of distinct chemical behaviour using resins. Four fractions were obtained from each water source and were organics absorbed to: (1) XAD-8 (very hydrophobic acids, VHA); (2) DAX-4 (slightly hydrophobic acids, SHA); (3) bound to an anion exchange resin (charged organics, CHAR); and (4) not absorbed or bound to resins (neutrals, NEUT). These fractions were then tested to determine the capacity of alum to remove them from water and to correlate this with the character of each isolate. The fractions were characterised by the application of high performance size exclusion chromatography (HPSEC), bacterial regrowth potential (BRP), trihalomethane formation potential (THMFP), pyrolysis gas-chromatography mass spectrometry (Py-GC-MS) and thermochemolysis. The highest removals of dissolved organic carbon (DOC) by alum treatment were in waters spiked with the CHAR fractions while the NEUT fractions were the most recalcitrant. The number average molecular weights (Mn) of DOC of the CHAR fractions before treatment were the highest, whilst those of the NEUT fractions were the lowest. After alum treatment, the Mn of the NEUT fractions were only slightly reduced. Results from Py-GC-MS and thermochemolysis indicate that the NEUT fractions had the highest relative proportion of saccharide derived organic material. Nonetheless, the BRP of waters spiked with the NEUT fractions differed markedly, indicating that organics recalcitrant to alum treatment can vary substantially in their chemical composition and capacity to support microbial growth.


Membranes ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 968
Author(s):  
Zhun Ma ◽  
Lu Zhang ◽  
Ying Liu ◽  
Xiaosheng Ji ◽  
Yuting Xu ◽  
...  

The fouling mechanism of the anion exchange membrane (AEM) induced by natural organic matter (NOM) in the absence and presence of calcium ions was systematically investigated via the extended Derjaguin–Landau–Verwey–Overbeek (xDLVO) approach. Sodium alginate (SA), humic acid (HA), and bovine serum albumin (BSA) were utilized as model NOM fractions. The results indicated that the presence of calcium ions tremendously aggravated the NOM fouling on the anion exchange membrane because of Ca-NOM complex formation. Furthermore, analysis of the interaction energy between the membrane surface and foulants via xDLVO revealed that short-range acid–base (AB) interaction energy played a significant role in the compositions of interaction energy during the electrodialysis (ED) process. The influence of NOM fractions in the presence of calcium ions on membrane fouling followed the order: SA > BSA > HA. This study demonstrated that the interaction energy was a dominating indicator for evaluating the tendency of anion exchange membranes fouling by natural organic matter.


2019 ◽  
Vol 5 (12) ◽  
pp. 2242-2250
Author(s):  
Xue Shen ◽  
Baoyu Gao ◽  
Kangying Guo ◽  
Qinyan Yue

Coagulation prior to the ultrafiltration (UF) process was implemented to improve natural organic matter (NOM) removal and membrane permeability.


2004 ◽  
Vol 50 (12) ◽  
pp. 279-285 ◽  
Author(s):  
J.H. Kweon ◽  
D.F. Lawler

The biggest impediment for applying membrane processes is fouling that comes from mass flux (such as particle and organic matter) to the membrane surface and its pores. Numerous research articles have indicated that either particles or natural organic matter (NOM) has been the most detrimental foulant. Therefore, the role of particles in membrane fouling was investigated with two synthetic waters (having either particles alone or particles with simple organic matter) and a natural water. Membrane fouling was evaluated with flux decline behavior and direct images from scanning electron microscopy. The results showed that the combined fouling by kaolin and dextran (a simple organic compound selected as a surrogate for NOM) showed no difference from the fouling with only the organic matter. The similarity might stem from the fact that dextran (i.e., polysaccharide) has no ability to be adsorbed on the clay material, so that the polysaccharide behaves the same with respect to the membrane with or without clay material being present. In contrast to kaolin, the natural particles showed a dramatic effect on membrane fouling.


1999 ◽  
Vol 40 (9) ◽  
pp. 113-120 ◽  
Author(s):  
A. Maartens ◽  
P. Swart ◽  
E. P. Jacobs

Organic matter in natural brown water as well as humic acids from a commercial sample were characterised by ultraviolet-visible light-spectroscopy and used in ultrafiltration studies. During ultrafiltration the pure-water flux and the operational flux were measured continuously to determine the degree of membrane fouling. The natural organic matter and commercial humic acid concentrations of the feed and permeate solutions were determined spectrophotometrically. These variables were used in conjunction with conventional flux measurements, to determine the colour-removal efficiency of ultrafiltration as well as the degree of foulant adsorption onto the membranes. Fouled membranes were cleaned with alkaline chemical agents normally used to extract natural organic matter from soil samples. The cleaning efficiency and the effect of cleaning solutions on the membrane selectivity were studied.


2017 ◽  
Vol 30 (1) ◽  
pp. 1-10 ◽  
Author(s):  
Thi Thu Nga Vu ◽  
Manon Montaner ◽  
Christelle Guigui

Wastewater effluents can be treated by an integrated membrane system combining membrane bioreactor (MBR) and reverse osmosis (RO) for effective removal of micropollutants in the field of high-quality water reuse. However, discharging the RO concentrate waste stream directly into the natural environment could lead to serious problems due to the toxic components contained in the concentrates (micropollutants, salts, organic matter). A possible solution could be the recirculation of RO concentrate waste to the MBR. However, such an operation should be studied in detail since the recirculation of non-biodegradable organic matter or high concentrations of salts and micropollutants could directly or indirectly contribute to MBR membrane fouling and modification of the biodegradation activity. In this context, the work reported here focused on the recirculation of such concentrates in an MBR, paying specific attention to MBR membrane fouling. Lab-scale experiments were performed on a continuous MBR-RO treatment line with RO concentrate recirculation. The main goal was to determine the recovery of the RO unit and of the global process that maintained good process performance in terms of biodegradation and MBR fouling. The results demonstrate that the impact of the toxic flow on activated sludge depends on the recovery of the RO step but the same trends were observed regardless of the organic matter and salt contents of the concentrates: the concentration of proteins increased slightly. Size-exclusion high performance liquid chromatography (HPLC-SEC) was employed to study the effects of RO concentrate on the production of protein-like soluble microbial products (SMPs) and demonstrated a significant peak of protein-like substances corresponding to 10-100 kDa and 100-1 000 kDa molecules in the supernatant. Thus a significant increase in the propensity for sludge fouling was observed, which could be attributed to the increased quantity of protein-like substances. Finally, the effect of the concentrate on sludge activity was studied and no significant effect was observed on biodegradation, indicating that the return of the concentrate to the MBR could be a good alternative.


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