Enhanced adsorption of Pb(II) by nitrogen and phosphorus co-doped biochar derived from Camellia oleifera shells

被引:75
作者
Fan, Youhua [1 ]
Wang, Hao [2 ]
Deng, Layun [1 ]
Wang, Yong [1 ]
Kang, Di [1 ]
Li, Changzhu [1 ]
Chen, Hong [3 ]
机构
[1] Hunan Acad Forestry, State Key Lab Utilizat Woody Oil Resource, Changsha 410004, Peoples R China
[2] Cent South Univ Forestry & Technol, Coll Mat Sci & Engn, Changsha 410004, Peoples R China
[3] Foshan Univ, Sch Mat Sci & Energy Engn, Foshan 528225, Peoples R China
关键词
Biochar; Co-doped; Adsorption selectivity; Adsorption mechanism; EFFICIENT FLAME-RETARDANT; AQUEOUS-SOLUTIONS; GRAPHENE OXIDE; HEAVY-METALS; HYDROTHERMAL CARBONIZATION; AMMONIUM POLYPHOSPHATE; SORPTION MECHANISMS; HIGH-PERFORMANCE; POROUS CARBON; REMOVAL;
D O I
10.1016/j.envres.2020.110030
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
We describe the synthesis of a series of novel nitrogen- and phosphorus-enriched biochar (activated carbon, AC) nanocomposites via the co-pyrolysis of Camellia oleifera shells (COSs) with different weight ratios of ammonium polyphosphate (APP) (w(APP): w(COSs) = 1-3:1). The physicochemical characteristics of these nanocomposites (APP@ACs) were investigated via X-ray diffraction (XRD), Raman spectroscopy, N-2 adsorption/desorption analysis, scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared spectroscopy (FTIR). The results revealed that the APP@ACs exhibited richer N- and P-containing functional groups than unmodified AC. In addition, the removal performance of APP@AC-3 with respect to Pb(II) (723.6 mg g(-1)) was greatly improved relative to unmodified AC (264.2 mg g(-1)). Kinetic and equilibrium data followed the pseudo-second-order kinetic model and Langmuir model, respectively. The removal mechanism could be attributed to partial physisorption and predominant chemisorption. The N-2 adsorption/desorption isotherms demonstrated that pore-volume properties could be an effective physical trap for Pb(II). Furthermore, the XPS and FTIR analysis revealed that the chemical removal mechanism of the APP@ACs is surface complexation via N-containing and P-containing functional groups. These findings indicate that the co-pyrolysis of COSs and APP leads to the formation of nitrogen- and phosphorus-containing functional groups that facilitate excellent activated carbon-based (biochar) adsorption performance.
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页数:11
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