Adsorption performance and mechanism of g-C3N4/UiO-66 composite for U(VI) from aqueous solution

被引:18
作者
Wu, Jiao [1 ,2 ]
Zheng, Zhouhao [2 ]
Zhu, Kaihao [2 ]
Xiang, Chao [2 ]
Wang, Jingsong [2 ]
Liu, Jinxiang [2 ]
机构
[1] Univ South China, Sch Civil Engn, Hunan Prov Key Lab Pollut Control & Resources Tec, Hengyang 421001, Peoples R China
[2] Univ South China, Sch Civil Engn, Hengyang 421001, Peoples R China
基金
中国国家自然科学基金;
关键词
Uranium (VI); Adsorption; Performance; g-C3N4; UiO-66; Mechanism; GRAPHITIC CARBON NITRIDE; METAL-ORGANIC FRAMEWORKS; G-C3N4; NANOSHEETS; URANIUM; REMOVAL; UIO-66; DEGRADATION; ENRICHMENT; REDUCTION; NANOTUBES;
D O I
10.1007/s10967-021-08116-w
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The uranium (VI) adsorption performance of g-C3N4/UiO-66 composite (CNUIO) was evaluated under different solution pH values, adsorbent dosages, coexisting ions, contact times, initial U(VI) concentrations, and temperatures. The surface properties and the interaction mechanism between U(VI) and CNUIO were analyzed via SEM-EDS, BET, FT-IR and XPS. CNUIO exhibited the maximum adsorption rate of 95.01% under the conditions of C-U(VI) = 10 mg/L, pH = 6, M/V = 0.4 g/L, t = 120 min, and T = 298 K, which was about 25% and 33.73% higher than that of g-C3N4 and UiO-66, respectively. The adsorption process was found to be a spontaneous endothermic process and conformed to the pseudo-second-order kinetic model and the Langmuir isothermal adsorption model. SEM-EDS and BET analysis revealed that increasing the specific surface area effectively improved the adsorption capacity of CNUIO. FT-IR spectroscopy and XPS indicated that the removal of U(VI) was attributed to the coordination complexation between the nitrogen-containing and the oxygen-containing functional groups of CNUIO and U(VI). Adsorption-desorption experiment demonstrated that CNUIO has a good reusability.
引用
收藏
页码:469 / 481
页数:13
相关论文
共 54 条
[21]   U(VI) capture from aqueous solution by highly porous and stable MOFs: UiO-66 and its amine derivative [J].
Luo, Bai-Cheng ;
Yuan, Li-Yong ;
Chai, Zhi-Fang ;
Shi, Wei-Qun ;
Tang, Quan .
JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY, 2016, 307 (01) :269-276
[22]   Aqueous Uranium(VI) Hydrolysis Species Characterized by Attenuated Total Reflection Fourier-Transform Infrared Spectroscopy [J].
Mueller, Katharina ;
Brendler, Vinzenz ;
Foerstendorf, Harald .
INORGANIC CHEMISTRY, 2008, 47 (21) :10127-10134
[23]   Uranium and molybdenum recovery from copper leaching solutions using, ion exchange [J].
Orrego, Pedro ;
Hernandez, Jose ;
Reyes, Alonso .
HYDROMETALLURGY, 2019, 184 :116-122
[24]   Modification of UiO-66 for removal of uranyl ion from aqueous solution by immobilization of tributyl phosphate [J].
Rajaei, Amir ;
Ghani, Kamal ;
Jafari, Mohammad .
JOURNAL OF CHEMICAL SCIENCES, 2021, 133 (01)
[25]  
Rong L., 2021, ACTA MATERIAE COMPOS, V39, P1
[26]   Synthesis of enhanced phosphonic functional groups mesoporous silica for uranium selective adsorption from aqueous solutions [J].
Sarafraz, H. ;
Minuchehr, A. ;
Alahyarizadeh, Gh. ;
Rahimi, Z. .
SCIENTIFIC REPORTS, 2017, 7
[27]   Aqueous suspensions of carbon nanotubes: Surface oxidation, colloidal stability and uranium sorption [J].
Schierz, A. ;
Zaenker, H. .
ENVIRONMENTAL POLLUTION, 2009, 157 (04) :1088-1094
[28]   Superior adsorption capacity of g-C3N4 for heavy metal ions from aqueous solutions [J].
Shen, Congcong ;
Chen, Changlun ;
Wen, Tao ;
Zhao, Zhiwei ;
Wang, Xiangke ;
Xu, Anwu .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2015, 456 :7-14
[29]   Improving the capability of UiO-66 for Cr(VI) adsorption from aqueous solutions by introducing isonicotinate N-oxide as the functional group [J].
Shokouhfar, Nasrin ;
Aboutorabi, Leila ;
Morsali, Ali .
DALTON TRANSACTIONS, 2018, 47 (41) :14549-14555
[30]   REPORTING PHYSISORPTION DATA FOR GAS SOLID SYSTEMS WITH SPECIAL REFERENCE TO THE DETERMINATION OF SURFACE-AREA AND POROSITY (RECOMMENDATIONS 1984) [J].
SING, KSW ;
EVERETT, DH ;
HAUL, RAW ;
MOSCOU, L ;
PIEROTTI, RA ;
ROUQUEROL, J ;
SIEMIENIEWSKA, T .
PURE AND APPLIED CHEMISTRY, 1985, 57 (04) :603-619