Enhanced removal and stepwise recovery of inorganic and organic micropollutants from water using novel graphene oxide doped multifunctional ß cyclodextrin chitosan polymer

被引:7
|
作者
Verma, Monu [1 ,2 ]
Hong, Youngmin [1 ,3 ]
Kumar, Vinod [2 ,4 ,8 ]
Bisht, Bhawna [2 ]
Vlaskin, Mikhail S. [5 ]
Chae, Seon-Ha [6 ]
Shah, Kinjal J. [7 ]
Kim, Hyunook [1 ]
机构
[1] Univ Seoul, Dept Environm Engn, Water Energy Nexus Lab, Seoul 02504, South Korea
[2] Grap Era Deemed Univ, Dept Food Sci & Technol, Dehra Dun 248002, Uttarakhand, India
[3] Shimadzu Sci Korea, Tech Res Ctr, 145 Gasan Digital 1 Ro, Seoul 08056, South Korea
[4] Peoples Friendship Univ Russia, RUDN Univ, Moscow 117198, Russia
[5] Russian Acad Sci, Joint Inst High Temp, 13-2 Izhorskaya St, Moscow 125412, Russia
[6] K Water, K Water Res Inst, Daejeon, South Korea
[7] Nanjing Tech Univ, Coll Urban Construct, Nanjing 211800, Peoples R China
[8] Grap Era Hill Univ, Dehra Dun 248002, Uttarakhand, India
基金
新加坡国家研究基金会;
关键词
Co-existing micropollutants; Heavy metals; Multifunctional polymer; Adsorption mechanism; Reusability; HEAVY-METAL IONS; ADSORPTION; ADSORBENT; EDTA; POLLUTANTS; CAPTURE; CD(II); PB(II); DYES;
D O I
10.1016/j.jpcs.2023.111615
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein, graphene oxide (GO) was successfully functionalized on the multifunctional ss cyclodextrin chitosan polymer through EDTA crosslinking (GO@CS EDTA ss CD) for the adsorption of toxic inorganic and organic micropollutants from water. This unique adsorbent possesses important adsorptive features from each component: chitosan works as a backbone of the polymer chain, ss CD cavities adsorb the organic micropollutants via the host-guest inclusion complexation, EDTA acts as a crosslinker and provides complexation sites for heavy metal ions and GO can interact with both organic and inorganic micropollutants. After complete characterization, the polymer were explored on the adsorption of inorganic micropollutants (i.e., Hg(II), Pb(II), Cu(II) and Ni (II)) and organic one (i.e., methylene blue, MB) under different experimental conditions. In monocomponent systems, the adsorption followed the pseudo-second order (PSO) kinetics for both heavy metals and MB dye. The adsorption isotherms of heavy metals and MB followed the Langmuir and Sips models, respectively. The maximum adsorption capacities were found to be 364.90 +/- 15.20, 287.40 +/- 10.0, 130.40 +/- 6.50, 98.90 +/- 3.10, 158.40 +/- 5.10 mg g(-1) for Hg(II), Pb(II), Cu(II), Ni(II) and MB, respectively. In binary component systems, dye adsorption was not affected by metal ions, while the adsorption efficiency for metal ions was increased by the MB presence: possibly due to synergism. Additionally, the prepared adsorbent showed good efficiency without any significant loss in adsorption capacity even after six continuous regeneration cycles, confirming its superior reusability and stability. In short, excellent removal efficiencies for the metal ions and MB at environmental levels in model textile effluent, synthetic acid mine water make the adsorbent promising in treating water contaminated by heavy metals and/or dyes.
引用
收藏
页数:12
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