热重分析
打赌理论
核化学
吸附
化学
生物炭
膨润土
比表面积
傅里叶变换红外光谱
最低杀菌浓度
扫描电子显微镜
分析化学(期刊)
作者
Hongyan Deng,Haixia He,Wen-Bin Li,Touqeer Abbas,Zhigang Liu
出处
期刊:PeerJ
[PeerJ]
日期:2022-03-01
卷期号:10: e13030-e13030
摘要
To realize simultaneous adsorption of heavy metal and antibiotic pollutants by a BC-based recyclable material, Fe 3 O 4 magnetic biochar (MBC) was prepared by co-precipitation method. Then different ratios of dodecyl dimethyl betaine (BS-12)-modified bentonite (BS-B) were loaded on the surfaces of biochar (BC) and MBC to prepare BS-B-loaded BC and MBC composites, called BS-B/BC and BS-B/MBC, respectively. The physicochemical and structural properties of the composites were characterized by scanning electron microscopy, Fourier transform infrared spectrometry, thermogravimetric analysis, specific surface area (S BET ) analysis, and vibrating sample magnetometry, and the adsorption efficiencies of BS-B/BC and BS-B/MBC to Cu 2+ and tetracycline (TC) were studied. The following results were obtained. (1) Compared with BS-B/BC, BS-B/MBC had decreased pH and cation exchange capacity (CEC) and increased S BET . The pH, CEC, and S BET of BS-B/BC and BS-B/MBC decreased with the increase in the BS-12 proportion of BS-B. The surface of BS-B/MBC became rough after Fe 3 O 4 loading. (2) The residual rate of BS-B/MBC was higher than that of BS-B/BC after high-temperature combustion, and the residual rate decreased with the increase in the BS-12 proportion of BS-B. The 2D infrared spectra showed that Fe 3 O 4 and BS-12 were modified on the surface of BS-B/MBC. MBC and BS-B/MBC had splendid magnetism and could be separated by external magnetic field. (3) Compared with unmagnetized ones, the adsorption effects of Cu 2+ and TC on different BS-B/MBCs improved, and the average adsorption rate reached the largest value of 91.92% and 97.76%, respectively. Cu 2+ and TC adsorptions were spontaneous, endothermic, and entropy-increasing processes. The pH and S BET of the material had a great influence on Cu 2+ and TC adsorptions, respectively, than CEC.
科研通智能强力驱动
Strongly Powered by AbleSci AI