Synergistic effect of a triethanolamine-modified carbon-based layered double hydroxide for efficient removal of nitrate from micro-polluted water

被引:3
作者
Pei, Yanyan [1 ,2 ]
Wang, Yanqu [1 ]
Jiao, Chengyuan [1 ]
Wang, Yuchang [1 ]
Jiang, Zhuwu [1 ]
机构
[1] Fujian Univ Technol, Coll Ecol Environm & Urban Construction, Fuzhou 350118, Fujian, Peoples R China
[2] CSCEC Strait Construct & Dev Co Ltd, Fuzhou 350015, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
GRAPHENE OXIDE; WASTE-WATER; ADSORPTION; COMPOSITE; PERFORMANCE; PHOSPHATE; ION; LDH; NANOCOMPOSITE; ADSORBENTS;
D O I
10.1039/d2dt02927h
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Owing to the ubiquitous existence and low concentrations of detrimental nitrogen pollutants in micro-polluted water, simple adsorption-oriented approaches are becoming increasingly appealing for the effective removal of NO3- from wastewater. Triethanolamine (TDA) modified carbon-based layered double hydroxide (LDH) composites (TDA@LDH/CS) were synthesized by a supersaturated co-precipitation method for efficient NO3- adsorption. The characterization results showed that TDA@LDH/CS, formed by the stacking of irregular nanosheets and lamellar aggregates, has a mesoporous structure and a specific surface area of 67.15 m(2) g(-1). The Langmuir and pseudo-second-order kinetic models were well fitted with the adsorption of NO3- by TDA@LDH/CS, with the maximum adsorption capacity reaching 14.45 mg g(-1), and the adsorption process was consistent with the spontaneous exothermic entropy increasement. Furthermore, the synergistic adsorption mechanism of NO3- by the TDA-modified materials was proposed using XPS analysis, which indicated that TDA modification greatly enriched the surface of TDA@LDH/CS with tertiary amine groups (R3N) and hydroxyl groups (-OH), providing more adsorption sites and active sites. After five cycles, the NO3- removal rate could still reach 64.2%, which exhibited its high potential to be utilized as an adsorbent for the removal of nitrogen pollutants from micro-polluted water.
引用
收藏
页码:17642 / 17652
页数:11
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