Facile synthesis of multifunctional bone biochar composites decorated with Fe/Mn oxide micro-nanoparticles: Physicochemical properties, heavy metals sorption behavior and mechanism
Xiao, Jiang2; Hu, Rui1; Chen, Guangcai2; Xing, Baoshan3
刊名JOURNAL OF HAZARDOUS MATERIALS
2020-11-15
卷号399
关键词Bone biochar FeOx/MnOx Heavy metals Wastes utilization Adsorption mechanism
ISSN号0304-3894
DOI10.1016/j.jhazmat.2020.123067
通讯作者Chen, Guangcai(guangcaichen@sohu.com)
英文摘要The value-added utilization of waste resources to synthesize functional materials is important to achieve the environmentally sustainable development. In this work, novel micro-nano FeOx- and MnOx-modified bone biochars derived from waste bone meal were obtained at 300 degrees C, 450 degrees C and 600 degrees C, and applied to remove Cd (II), Cu(II) and Pb(II) from aqueous solutions. The results showed that the pyrolysis temperature greatly influenced the specific surface area (SSA), micropore creation, functional groups and heavy metal sorption capacities of FO-BCs and MO-BCs. The effects of solution pH, ionic strength, humic acid (HA), kinetics and thermodynamics on heavy metals adsorption were investigated. Langmuir and pseudo-second order kinetics models fit the adsorption data well, and the FO-BC-450 and MO-BC-600 displayed the highest sorption capacity for Cd(II) (151.3 mg/g and 163.4 mg/g), Cu(II) (219.8 mg/g and 259.0 mg/g) and Pb(II) (271.9 mg/g and 407.2 mg/g), respectively. Due to the dissolved partial hydroxyapatite (HAP), carbonate-bearing hydroxyapatite (CHAP) and the catalysis of Fe(NO3)(3), the FO-BCs with higher SSA than the MO-BCs, whereas the sorption capacity displayed an opposite trend. The chemical complex, cation-pi bonds, ion exchange and coprecipitation were the dominant mechanisms for metals adsorption. Overall, waste bone resource co-pyrolysis with Fe(NO3)(3)/KMnO4 impregnation is a promising and high-efficient adsorbents for the remediation of heavy metals-contaminated waters.
资助项目Fundament Research Funds of CAF[CAFYBB2019SZ001] ; China Postdoctoral Science Foundation[2018M640200] ; China Postdoctoral Science Foundation[2019T120154] ; Key Research and Development Program of Zhejiang Province[2018C03047] ; CAS Pioneer Hundred Talents Program ; CASHIPS Director's Fund[YZJJ2018QN20] ; National Natural Science Foundation of China[21875257]
WOS关键词ZERO-VALENT IRON ; AQUEOUS-SOLUTIONS ; MAGNETIC BIOCHAR ; LOADED BIOCHAR ; ADSORPTION ; REMOVAL ; LEAD ; CADMIUM ; CD(II) ; PYROLYSIS
WOS研究方向Engineering ; Environmental Sciences & Ecology
语种英语
出版者ELSEVIER
WOS记录号WOS:000569380400008
资助机构Fundament Research Funds of CAF ; China Postdoctoral Science Foundation ; Key Research and Development Program of Zhejiang Province ; CAS Pioneer Hundred Talents Program ; CASHIPS Director's Fund ; National Natural Science Foundation of China
内容类型期刊论文
源URL[http://ir.hfcas.ac.cn:8080/handle/334002/104121]  
专题中国科学院合肥物质科学研究院
通讯作者Chen, Guangcai
作者单位1.Chinese Acad Sci, Inst Appl Technol, Hefei Inst Phys Sci, Hefei 230088, Peoples R China
2.Chinese Acad Forestry, Res Inst Subtrop Forestry, Hangzhou 311400, Zhejiang, Peoples R China
3.Univ Massachusetts, Stockbridge Sch Agr, Amherst, MA 01003 USA
推荐引用方式
GB/T 7714
Xiao, Jiang,Hu, Rui,Chen, Guangcai,et al. Facile synthesis of multifunctional bone biochar composites decorated with Fe/Mn oxide micro-nanoparticles: Physicochemical properties, heavy metals sorption behavior and mechanism[J]. JOURNAL OF HAZARDOUS MATERIALS,2020,399.
APA Xiao, Jiang,Hu, Rui,Chen, Guangcai,&Xing, Baoshan.(2020).Facile synthesis of multifunctional bone biochar composites decorated with Fe/Mn oxide micro-nanoparticles: Physicochemical properties, heavy metals sorption behavior and mechanism.JOURNAL OF HAZARDOUS MATERIALS,399.
MLA Xiao, Jiang,et al."Facile synthesis of multifunctional bone biochar composites decorated with Fe/Mn oxide micro-nanoparticles: Physicochemical properties, heavy metals sorption behavior and mechanism".JOURNAL OF HAZARDOUS MATERIALS 399(2020).
个性服务
查看访问统计
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。


©版权所有 ©2017 CSpace - Powered by CSpace