TY - JOUR
T1 - Qualitative and relative distribution of Pb2+ adsorption mechanisms by biochars produced from a fluidized bed pyrolysis system under mild air oxidization conditions
AU - Liu, Lingqin
AU - Huang, Yaji
AU - Cao, Jianhua
AU - Hu, Huajun
AU - Dong, Lu
AU - Zha, Jianrui
AU - Su, Yinhai
AU - Ruan, Roger
AU - Tao, Shengnian
N1 - Publisher Copyright:
© 2020 Elsevier B.V.
PY - 2021/2/1
Y1 - 2021/2/1
N2 - Qualitative and relative distribution of Pb2+ adsorption mechanisms was investigated using corn stalk biochars (CSBs) and rice husk biochars (RHBs) produced from a pilot-scale fluidized bed pyrolysis system under mild air oxidization conditions (oxygen content 0–6%) at low temperature (450 °C). Boehm titration, Fourier Transform Infrared Spectroscopy (FTIR), X-ray Photoelectron Spectroscopy (XPS), and Scanning Electron Microscope with Energy Dispersive Spectrometer (SEM-EDS) were used to analyze the characteristics of biochars, and adsorption isotherms and kinetics analysis were studied. The Pb2+ adsorption capacities of CSBs (about 40 mg/g) presented about twice the amount of RHBs (about 22 mg/g), which were mainly caused by cation exchange and precipitation mechanisms, with the contribution content to the total sorption up to 90%. With oxygen content increasing from 0% to 6%, the absorbed lead capacity due to cation exchange of CSBs increased from 19.10 to 30.40 mg/g, and the corresponding contributions to total Pb2+ sorption increased from 49.00% to 73.80%. When the oxygen content of pyrolysis atmosphere increased, the contribution of cation exchange in Pb2+ adsorption exhibited extremely different tendencies in CSBs and RHBs under the combined action of metallic accumulation in ash and non-active silica embedding in the retract process, which plays a dominant role in Pb2+ adsorption. This study suggests that CSBs produced by fluidized bed under mild air oxidation improved cation exchange capacity, and were promising, low-cost biochar for Pb2+ remediation in the aqueous environment.
AB - Qualitative and relative distribution of Pb2+ adsorption mechanisms was investigated using corn stalk biochars (CSBs) and rice husk biochars (RHBs) produced from a pilot-scale fluidized bed pyrolysis system under mild air oxidization conditions (oxygen content 0–6%) at low temperature (450 °C). Boehm titration, Fourier Transform Infrared Spectroscopy (FTIR), X-ray Photoelectron Spectroscopy (XPS), and Scanning Electron Microscope with Energy Dispersive Spectrometer (SEM-EDS) were used to analyze the characteristics of biochars, and adsorption isotherms and kinetics analysis were studied. The Pb2+ adsorption capacities of CSBs (about 40 mg/g) presented about twice the amount of RHBs (about 22 mg/g), which were mainly caused by cation exchange and precipitation mechanisms, with the contribution content to the total sorption up to 90%. With oxygen content increasing from 0% to 6%, the absorbed lead capacity due to cation exchange of CSBs increased from 19.10 to 30.40 mg/g, and the corresponding contributions to total Pb2+ sorption increased from 49.00% to 73.80%. When the oxygen content of pyrolysis atmosphere increased, the contribution of cation exchange in Pb2+ adsorption exhibited extremely different tendencies in CSBs and RHBs under the combined action of metallic accumulation in ash and non-active silica embedding in the retract process, which plays a dominant role in Pb2+ adsorption. This study suggests that CSBs produced by fluidized bed under mild air oxidation improved cation exchange capacity, and were promising, low-cost biochar for Pb2+ remediation in the aqueous environment.
KW - Adsorption mechanisms
KW - Biochar
KW - Fluidized bed pyrolysis
KW - Lead adsorption
KW - Mild air oxidization
KW - Relative contribution
UR - https://www.scopus.com/pages/publications/85097111722
UR - https://www.scopus.com/pages/publications/85097111722#tab=citedBy
U2 - 10.1016/j.molliq.2020.114600
DO - 10.1016/j.molliq.2020.114600
M3 - Article
AN - SCOPUS:85097111722
SN - 0167-7322
VL - 323
JO - Journal of Molecular Liquids
JF - Journal of Molecular Liquids
M1 - 114600
ER -