Effect of Surface-Exposed Chemical Groups on Calcium-Phosphate Mineralization in Water-Treatment Systems

被引:48
作者
Steiner, Zvi [2 ]
Rapaport, Hanna [1 ]
Oren, Yoram [2 ]
Kasher, Roni [2 ]
机构
[1] Ben Gurion Univ Negev, Dept Biotechnol Engn, IL-84105 Beer Sheva, Israel
[2] Ben Gurion Univ Negev, Jacob Blaustein Inst Desert Res, Zuckerberg Inst Water Res, Dept Desalinat & Water Treatment, IL-84990 Sede Boqer, Israel
关键词
NATURAL ORGANIC-MATTER; NANOFILTRATION MEMBRANES; WASTE-WATER; HYDROXYAPATITE; MONOLAYERS; DESALINATION; SPECTROSCOPY; MECHANISMS; ADSORPTION; PROTEINS;
D O I
10.1021/es101773t
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Calcium-phosphate-scale formation on reverse osmosis (RO) membranes is a major limiting factor for cost-effective desalination of wastewater. We determined the effects of various organic chemical groups found on membrane surfaces on calcium-phosphate scaling. Langmuir films exposing different functional groups were equilibrated with a solution simulating the ionic profile of secondary effluent (SSE). Surface pressure-area (Langmuir) isotherms combined with ICP elemental analyses of the interfacial precipitate suggested acceleration of calcium-phosphate mineralization by the surface functional groups in the order: PO4 > COOH similar to NH2 > COOH:NH2 (1:1) > OH > ethylene glycol. Immersion of gold-coated silicon wafers self-assembled with different alkanethiols in SSE solution showed formation of a hydroxyapatite precipitate by X-ray diffraction and ATR-IR analysis. Data showed diverse influences of functional groups on mineralization, implying low calcium-phosphate scaling for uncharged surfaces or surfaces coated with both positively and negatively charged groups. This information is valuable for understanding scaling processes, and for designing of novel low-scaling membranes for water desalination.
引用
收藏
页码:7937 / 7943
页数:7
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