Effects of reverse osmosis isolation on reactivity of naturally occurring dissolved organic matter in physicochemical processes

被引:34
作者
Kilduff, JE
Mattaraj, S
Wigton, A
Kitis, M
Karanfil, T
机构
[1] Rensselaer Polytech Inst, Dept Civil & Environm Engn, Troy, NY 12180 USA
[2] Ubon Ratchathani Univ, Fac Engn Chem Engn, Ubon Ratchathani 34190, Thailand
[3] Suleyman Demirel Univ, Dept Environm Engn, TR-32200 Isparta, Turkey
[4] Clemson Univ, Dept Environm Sci & Engn, Anderson, SC 29625 USA
基金
美国国家科学基金会; 美国国家环境保护局;
关键词
reverse osmosis; natural organic matter; isolation; organic carbon; fouling; nanofiltration; preloading; size exclusion chromatography;
D O I
10.1016/j.watres.2003.10.049
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A field reverse osmosis system was used to isolate dissolved organic matter (DOM) from two lacustrine and two riverine surface water sources. The rejection of DOM was on the order of 99% and did not vary significantly with pressure. A simple mass balance model using a single measured value of rejection predicted the concentration within the closed-loop isolation system. The effect of operating pressure and solution flux on mass recovery of DOM was evaluated in laboratory and field trials. Under controlled laboratory conditions, >99% of a lacustrine DOM could be accounted for. A fraction of the isolated DOM was not recoverable using hydrodynamic cleaning; however, this fraction was recovered by using a pH 10 NaOH wash solution. The mass recovered in the NaOH solution increased from <1% to >6% with increasing transmembrane pressures from 414 kPa (60 psi) to 1000 kPa (145 psi), respectively. This is consistent with fouling that results from an increase in solution flux, and a decrease in tangential crossflow velocity. Under field conditions, mass balances were generally >95% and mass recovery was >90% in all cases. The effects of temperature on solution flux were consistent with changes in fluid viscosity; effects of temperature on membrane diffusivity or morphological properties were small. RO isolation under low pressure conditions designed to maximize DOM recovery had little effect on DOM reactivity evaluated in terms of nanofiltration membrane fouling, XAD-8 resin adsorption, activated carbon adsorption, competition with trichloroethylene for adsorption sites on activated carbon, and molecular weight distribution measured using size exclusion chromatography. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1026 / 1036
页数:11
相关论文
共 27 条
[1]  
[Anonymous], 1995, Standard methods for the examination of water and wastewater, V19th
[2]   Nanofiltration of natural organic matter: pH and ionic strength effects [J].
Braghetta, A ;
DiGiano, FA ;
Ball, WP .
JOURNAL OF ENVIRONMENTAL ENGINEERING-ASCE, 1997, 123 (07) :628-641
[3]   USE OF ULTRAFILTRATION FOR SEPARATION AND FRACTIONATION OF ORGANIC-LIGANDS IN FRESH WATERS [J].
BUFFLE, J ;
DELADOEY, P ;
HAERDI, W .
ANALYTICA CHIMICA ACTA, 1978, 101 (02) :339-357
[4]  
CARTER MC, 1992, J AM WATER WORKS ASS, V84, P81
[5]   SITE ENERGY-DISTRIBUTION ANALYSIS OF PRELOADED ADSORBENTS [J].
CARTER, MC ;
KILDUFF, JE ;
WEBER, WJ .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1995, 29 (07) :1773-1780
[6]   MOLECULAR-WEIGHT, POLYDISPERSITY, AND SPECTROSCOPIC PROPERTIES OF AQUATIC HUMIC SUBSTANCES [J].
CHIN, YP ;
AIKEN, G ;
OLOUGHLIN, E .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1994, 28 (11) :1853-1858
[7]   Membrane filtration of natural organic matter: factors and mechanisms affecting rejection and flux decline with charged ultrafiltration (UF) membrane [J].
Cho, J ;
Amy, G ;
Pellegrino, J .
JOURNAL OF MEMBRANE SCIENCE, 2000, 164 (1-2) :89-110
[8]   CONCENTRATION OF AQUATIC DISSOLVED ORGANIC-MATTER BY REVERSE-OSMOSIS [J].
CLAIR, TA ;
KRAMER, JR ;
SYDOR, M ;
EATON, D .
WATER RESEARCH, 1991, 25 (09) :1033-1037
[9]   Chemical and physical aspects of natural organic matter (NOM) fouling of nanofiltration membranes [J].
Hong, SK ;
Elimelech, M .
JOURNAL OF MEMBRANE SCIENCE, 1997, 132 (02) :159-181
[10]   ADSORPTION OF AQUATIC HUMIC SUBSTANCES ON HYDROPHOBIC ULTRAFILTRATION MEMBRANES [J].
JUCKER, C ;
CLARK, MM .
JOURNAL OF MEMBRANE SCIENCE, 1994, 97 :37-52