Effective natural organic matter removal in pond water by carbon nanotube membrane with flocculation/adsorption

被引:3
|
作者
Lee, Jieun [1 ]
Vigneswaran, Saravanamuth [2 ]
Zhang, Yongshun [1 ]
Reddy, Ramireddy S. P. Raj [1 ]
Liu, Zongwen [1 ]
机构
[1] Univ Sydney, Sch Chem & Biomol Engn, Sydney, NSW 2006, Australia
[2] UTS, Fac Engn & IT, POB 123, Broadway, NSW 2007, Australia
来源
关键词
adsorption; carbon nanotube membrane; flocculation; membrane hybrid system; natural organic matter removal; ultrafiltration membrane; ULTRAFILTRATION PROCESS; SURFACE-WATER; COAGULATION; NOM; PRETREATMENT; CHLORIDE; PERFORMANCE; ADSORPTION; SYSTEM; IMPACT;
D O I
10.2166/ws.2017.005
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A carbon nanotube (CNT) ultrafiltration (UF) membrane was applied to natural organic matter (NOM) removal in pond water treatment. The source water was pretreated by flocculation and/or adsorption prior to the UF process to alleviate permeate flux decline and improve NOM removal efficiency. The performance of a commercial polyethersulfone (PES) UF membrane was compared to evaluate that of the CNT membrane. The CNTmembrane outperformed the PES-UF membrane. The permeate flux, total organic carbon and humic acid (HA) removal rate of the CNT membrane was observed to be 230 LMH/ bar, 60%, and 80% when 30mg/L poly aluminium chloride (PACI) flocculation was applied. This highlights that the permeate flux was three times higher with slightly higher rejection efficiency than the PES-UF membrane. In particular, severe permeate flux decline was completely overcome by the CNT membrane with 30mg/L PACI coagulation. For powder activated carbon (PAC) adsorption, even though there was a severe permeate flux decline in the CNT membrane, almost complete HA removal (98%) was achieved when 0.5 g/L PAC adsorption was coupled. Based on the superior performance of the CNT membrane with pretreatment, the CNT membrane is suggested to be a robust system for a high concentration of organic matter pond water treatment without membrane flux decline.
引用
收藏
页码:1080 / 1087
页数:8
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