吸附
化学
扫描电子显微镜
吸热过程
碳化
核化学
朗缪尔吸附模型
透射电子显微镜
解吸
无机化学
化学工程
物理化学
材料科学
纳米技术
工程类
复合材料
作者
Yan Liu,Yunfei Ouyang,Dejuan Huang,Chao Jiang,Xiaopeng Liu,Yun Wang,Ying Dai,Dingzhong Yuan,Jia Wei Chew
标识
DOI:10.1016/j.scitotenv.2019.136019
摘要
Herein, the precursor polyphosphazene was synthesized by the polymerization of hexachlorocyclotriphosphazene (HCCP) and bis(4-hydroxyphenyl) sulfone (BPS). The adsorbent which was codoped with N, P and S (amidate-CS) was developed from the precursor by using the carbonization method. The images of Scanning electron microscope (SEM) and Transmission electron microscope (TEM) indicate that the amidate-CS possessed porous graphene-like carbon lamellar structure. The excellent behaviors with respect to kinetics (120 min for equilibrium) and thermodynamics (maximum removal of 290 mg/g when pH was at 6.0) revealed the outstanding performance of amidate-CS in removing U(VI), which is due to the functional groups and strong covalent bonds between heteroatoms and uranyl ions. The adsorption of amidate-CS followed the pseudo-second-order kinetic and Langmuir adsorption model. The thermodynamic parameters indicate that the process was spontaneous and endothermic. The adsorption and desorption efficiency of amidate-CS had a slight decrease after five cycles, indicating excellent regeneration performance. Overall, the amidate-CS is a prospective candidate for highly selective U(VI) removing.
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