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活性焦吸附处理五氯酚钠废水

Adsorption of sodium pentachlorophenate wastewater on activated coke
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摘要 以活性焦为吸附剂,采用静态吸附实验考察活性焦对PCP-Na模拟废水的吸附性能,研究了反应时间、温度、p H值、活性焦用量对吸附效果的影响,采用急性毒性法评价吸附前后废水急性毒性的变化.结果表明,在原始p H下,温度40℃,活性焦用量4 g·L-1,反应时间180 min时,废水中PCP-Na的浓度由100 mg·L-1降为2.92 mg·L-1,去除率97.07%.吸附后废水的急性毒性下降99.09%.PCP-Na在活性焦表面的吸附是拟二级反应,吸附速率常数为2.52×10-2g·mg-1·min-1,其吸附行为可用Langmuir等温线模型进行描述;热力学计算结果表明吸附反应是自发和吸热过程. Sodium pentachlorophenate( PCP-Na) wastewater is highly toxic and poorly degradable.Static adsorption test was conducted to investigate the adsorption properties of activated coke( AC)for treatment of PCP-Na simulated wastewater. The effect of contact time,temperature,p H and activated coke dosage on PCP-Na removal was studied. Under the conditions of initial p H and 40 ℃,the concentration of PCP-Na decreased from 100 to 2. 92 mg·L- 1after 180 min of contact with the AC dosage of 4g·L- 1,The acute toxicity was reduced by 99. 09% after adsorption. The adsorption kinetics of PCP-Na on AC was coincident with pseudo second- order and the rate constant was 2. 52 ×10- 2g·mg- 1·min- 1. The Langmuir isotherm can be used to describe the adsorption process. The thermodynamic analytical results indicated that the adsorption was spontaneous and endothermic.
出处 《环境化学》 CAS CSCD 北大核心 2015年第8期1545-1552,共8页 Environmental Chemistry
关键词 活性焦 五氯酚钠 吸附动力学 吸附热力学 急性毒性 activated coke sodium pentachlorophenate adsorption kinetics adsorption thermodynamics acute toxicity
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  • 1Zhang L J, Hu C W, Wang W L, et al. Acute toxicity of multi-walled carbon nanotubes, sodium pentaehlorophenate, and their complex on earthworm Eisenia fetida[ J]. Ecotoxicology and Environmental Safety, 2014, 103:29-35.
  • 2Muir J, Eduljee G. PCP in the freshwater and marine environment of the European Union [ J ]. The Science of the Total Environment, 1999, 236(1-3) : 41-56.
  • 3Zeng L, McKinley J W. Degradation of pentachlornphenol in aqueous solution by audible-frequency sonolytic ozonation [ J ]. Journal of Hazardous Materials, 2006, 135(1-3) : 218-225.
  • 4Hong P K, Zeng Y. Degradation of pentachlorophenol by ozonation and biodegradability of intermediates [ J ]. Water Research, 2002, 36 (17) : 4243-4254.
  • 5Benitez F J, Aeero J L, Real F J, et al. Kinetics of photodegradation and ozonation of pentaehlorophenol[ J ]. Chemosphere, 2003,5 l (8) : 651-662.
  • 6Wang J L, Yu ~, Zhang L Z. Highly efficient photocatalytic removal of sodium pentachlorophenate with Bi304Br under visible light[ J]. Applied Catalysis B : Environmental, 2013, 136-137:112-121.
  • 7Gunlazuardi J, Lindu W A. Photoeatalytie degradation of pentachlorophenol in aqueous solution employing immobilized TiO2 supported on titanium metal [ J]. Journal of Photochemistry and Photobiology A: Chemistry, 2005, 173 (1) : 51-55.
  • 8Pecehi G, Reyes P, Sanhueza P, et al. Photocatalytie degradation of pentachlorophenol on TiO2 sol-gel catalysts [ J ]. Chenmsphere, 2001, 43(2) : 141-146.
  • 9Quan x, Ruan X L, Zhao H M, et al. Photoeleetrocatalytie degradation of pentaehlorophenol in aqueous solution using a TiO2 nanotube film electrode[ J]. Environmental pollution, 2007, 147(2) : 409-414.
  • 10Chang X F, Ji G B, Sui Q, et al. Rapid photocatalytic degradation of PCP-Na over NaBiO3 driven by visible light irradiation[ J ]. Journal of Hazardous Materials, 2009, 166(2-3): 728-733.

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