TY - JOUR
T1 - A hybridized photocatalysis-microfiltration system with iron oxide-coated membranes for the removal of natural organic matter in water treatment
T2 - Effects of iron oxide layers and colloids
AU - Yao, Ping
AU - Choo, Kwang Ho
AU - Kim, Moon Hyeon
PY - 2009/9
Y1 - 2009/9
N2 - A photocatalysis/microfiltration (MF) hybrid system, with the coating of a membrane using iron oxide particles (IOPs), was investigated with respect to natural organic matter (NOM) removal and membrane permeability during the treatment of various surface waters. A comparison of the performance between bare (uncoated) and IOP-coated membranes employed for the photocatalytic hybrid system was made. Due to the additional adsorption of NOM onto IOPs on the membrane surface, the IOP-coated membrane system always achieved greater DOC removal efficiencies during photocatalysis/MF. Particularly, the influence of colloidal particles that were present in different water sources with respect to membrane fouling was explored. Colloidal fouling occurred to both bare and IOP-coated membranes, but the interaction of colloids with IOP coating layers was in close association with the characteristics of colloids, such as size distribution, resulting in opposing fouling behaviors with varying water sources. The IOP-coated membrane was able to control fouling properly when a relatively large size of colloidal particles existed in raw water, but not for the case of small colloids. The IOP coat layer may become denser as small colloids penetrate into it, therefore leading to further fouling. The analysis of the hydraulic filtration resistances revealed that such fouling was virtually reversible in being removed by backwashing processes. Scanning electron microscopic observations, however, visualized the existence of several foulants remaining at the membrane surface after backwashing when feed water, containing a relatively large portion of small-sized colloids, was supplied.
AB - A photocatalysis/microfiltration (MF) hybrid system, with the coating of a membrane using iron oxide particles (IOPs), was investigated with respect to natural organic matter (NOM) removal and membrane permeability during the treatment of various surface waters. A comparison of the performance between bare (uncoated) and IOP-coated membranes employed for the photocatalytic hybrid system was made. Due to the additional adsorption of NOM onto IOPs on the membrane surface, the IOP-coated membrane system always achieved greater DOC removal efficiencies during photocatalysis/MF. Particularly, the influence of colloidal particles that were present in different water sources with respect to membrane fouling was explored. Colloidal fouling occurred to both bare and IOP-coated membranes, but the interaction of colloids with IOP coating layers was in close association with the characteristics of colloids, such as size distribution, resulting in opposing fouling behaviors with varying water sources. The IOP-coated membrane was able to control fouling properly when a relatively large size of colloidal particles existed in raw water, but not for the case of small colloids. The IOP coat layer may become denser as small colloids penetrate into it, therefore leading to further fouling. The analysis of the hydraulic filtration resistances revealed that such fouling was virtually reversible in being removed by backwashing processes. Scanning electron microscopic observations, however, visualized the existence of several foulants remaining at the membrane surface after backwashing when feed water, containing a relatively large portion of small-sized colloids, was supplied.
KW - Colloids
KW - Drinking water treatment
KW - Iron oxide particles
KW - Membrane coating
KW - Microfiltraiton
KW - Natural organic matter
KW - Photocatalysis
UR - http://www.scopus.com/inward/record.url?scp=69949108527&partnerID=8YFLogxK
U2 - 10.1016/j.watres.2009.06.010
DO - 10.1016/j.watres.2009.06.010
M3 - Article
C2 - 19576613
AN - SCOPUS:69949108527
SN - 0043-1354
VL - 43
SP - 4238
EP - 4248
JO - Water Research
JF - Water Research
IS - 17
ER -