Adsorption of p-chlorophenol and p-nitrophenol in single and binary systems from solution using magnetic activated carbon

被引:15
|
作者
Rong, Yachan [1 ]
Han, Runping [1 ]
机构
[1] Zhengzhou Univ, Coll Chem & Mol Engn, 100 Kexue Rd, Zhengzhou 450001, Henan, Peoples R China
关键词
Magnetic Activated Carbon; p-Chlorophenol; p-Nitrophenol; Competitive Adsorption; Desorption; AQUEOUS-SOLUTION; COMPETITIVE ADSORPTION; METHYLENE-BLUE; PHENOL; REMOVAL; BATCH; WATER; KINETICS; ACID; DYE;
D O I
10.1007/s11814-019-0267-1
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Magnetic activated carbon (MAC) was prepared by co-precipitation. These particles had attractive adsorption capacity and could be easily separated from aqueous. MAC was used as adsorbent to remove p-chlorophenol (p-CP) and p-nitrophenol (p-NP) from solution in single and binary systems. In a single system, the equilibrium time was 60 min, the best initial pH was 3-8 and 3-6 for p-CP or p-NP adsorption, respectively. The existence of salt ions had little influence on the adsorption process, while surfactant had negative influence. The adsorption quantity from experiments was up to 97.3 mgg(-1) for p-CP and 116 mgg(-1) for p-NP at 293 K, respectively. Freundlich model and pseudo-second-order kinetic model fitted well the adsorption behavior. Thermodynamic parameters were calculated and the results showed that the process was spontaneous, exothermic and entropy production in nature. In addition, p-CP or p-NP-loaded MAC could be well reused by 0.01 molL(-1) sodium hydroxide solution as regeneration agent. Kinetic process of desorption was fitted best by pseudo-second-order kinetic model. Results from the binary system showed that competitive adsorption existed during the process, and p-NP adsorption on MAC was easier than p-CP. Freundlich model well fitted the adsorption behavior in the binary system. Hydrogen-bonding, electron donor-acceptor and - interactions may be the main mechanisms of adsorption. MAC proved to be an excellent adsorbent for the removal of p-CP and p-NP from solution.
引用
收藏
页码:942 / 953
页数:12
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