Sludge carbonization and activation: From hazardous waste to functional materials for water treatment

被引:43
作者
Cheng, Fangwei [1 ]
Luo, Hongxi [1 ]
Hu, Lei [2 ]
Yu, Bin [2 ]
Luo, Zhen [2 ]
de Cortalezzi, Maria Fidalgo [3 ]
机构
[1] Univ Missouri Columbia, Dept Chem Engn, Columbia, MO 65211 USA
[2] CECEP Both Environm Engn & Tech Co Ltd, Wuhan 430071, Hubei, Peoples R China
[3] Univ Missouri Columbia, Dept Civil & Environm Engn, Columbia, MO 65211 USA
来源
JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING | 2016年 / 4卷 / 04期
关键词
Sustainability; Sludge; Carbonization; Water treatment; Adsorption; Sorbents;
D O I
10.1016/j.jece.2016.11.013
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The utilization of sludge from wastewater treatment plants as adsorbent material was investigated. Dry sludge from Ezhou Qingyuan sewage treatment plant (Hubei, China) was heated in anaerobic conditions to produce carbonized sludge, that further chemically activated at higher temperatures and K2CO3 to enhance porosity and surface area. The materials were characterized by scanning electron microscopy (SEM), Fourier transformed infrared spectroscopy (FTIR). thermo gravimetric analysis (TGA) and nitrogen adsorption isotherms. TGA curves showed water and low molecular weight organics were lost in a first stage, with the onset of decomposition at 300 degrees C and up to 700 degrees C; activation resulted in further carbonization. Nitrogen adsorption experiments yielded Type IV isotherms, characteristic of mesoporous materials. Activation greatly increased surface area, reaching up to 642 m(2)/g. FTIR spectra showed the formation of a carboxyl-metal complex at activation, but no further changes in functional groups with increasing reaction temperature. The adsorption capacities of carbonized and activated sludge towards Rhodamine B were investigated by batch and kinetic experiments. Adsorption increased with activation temperature, reaching a maximum at 700 degrees C with the exception of the sample carbonized at 500 degrees C where a monotonic increase in capacity was observed. Isotherms showed Langmuir-type behavior; kinetic data was successfully fitted to a pseudo second order model. The adsorption was not affected by pH changes or dissolved solids type and concentration. Zeta potential determinations showed minimal variation of surface charge in the pH range of interest. The results indicated that sludge carbonization is a promising sustainable technology for mass sludge treatment. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4574 / 4586
页数:13
相关论文
共 43 条
[1]   Anaerobic/aerobic treatment of municipal landfill leachate in sequential two-stage up-flow anaerobic sludge blanket reactor (UASB)/completely stirred tank reactor (CSTR) systems [J].
Agdag, ON ;
Sponza, DT .
PROCESS BIOCHEMISTRY, 2005, 40 (02) :895-902
[2]   SPECTROSCOPIC CHARACTERIZATION OF INDIAN STANDARD SAND [J].
Anbalagan, G. ;
Prabakaran, A. R. ;
Gunasekaran, S. .
JOURNAL OF APPLIED SPECTROSCOPY, 2010, 77 (01) :86-94
[3]   Principles and potential of the anaerobic digestion of waste-activated sludge [J].
Appels, Lise ;
Baeyens, Jan ;
Degreve, Jan ;
Dewil, Raf .
PROGRESS IN ENERGY AND COMBUSTION SCIENCE, 2008, 34 (06) :755-781
[4]   Pore structure and surface chemistry of adsorbents obtained by pyrolysis of sewage sludge-derived fertilizer [J].
Bagreev, A ;
Bandosz, TJ ;
Locke, DC .
CARBON, 2001, 39 (13) :1971-1979
[5]   Sewage sludge-derived materials as efficient adsorbents for removal of hydrogen sulfide [J].
Bagreev, A ;
Bashkova, S ;
Locke, DC ;
Bandosz, TJ .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2001, 35 (07) :1537-1543
[6]  
Bansal R.C.R.C., 2005, ACTIVATED CARBON ADS
[7]  
CECEP Both Environment Eng. & Tech. Co. L., 2015, PROP DRY SLUDG UNPUB
[8]  
CECEP Both Environment Eng. & Tech. Co. L., 2015, POSS APPL CARB UNPUB
[9]  
CECEP Both Environment Eng. & Tech. Co. L., 2012, STUD LEACH PRO UNPUB
[10]   Residue characteristics and pore development of petrochemical industry sludge pyrolysis [J].
Chiang, HL ;
Chao, CG ;
Chang, CY ;
Wang, CF ;
Chiang, PC .
WATER RESEARCH, 2001, 35 (18) :4331-4338