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声电协同氧化氯酚的实验研究 被引量:2

Experimental studies on chlorophenol decomposition with coupling ultrasound and electrocatalysis process
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摘要 采用超声波-电催化联合技术处理2-氯酚(2-CP)和4-氯酚(4-CP),探讨了电催化氧化和超声氧化的协同效应,考察了影响声电联合降解氯酚化合物的条件因数。结果表明,超声波-电催化联合技术处理效率明显优于电催化氧化技术,2-CP和4-CP的增强因子f分别为1.325和1.509。高电流密度有助于氯酚降解,2-CP和4-CP的表观反应速率常数随电流密度上升分别增加了1.28×10-5s-1和1.82×10-5s-1;高pH值也有利于氯酚降解,pH为9.08时,2-CP和4-CP的表观反应速率常数分别为9.22×10-5s-1和11.02×10-5s-1;高电解质浓度促进了2-CP的降解,而对4-CP的降解影响不大,2-CP表观反应速率常数从7.70×10-5s-1上升到16.03×10-5s-1。总之,超声波-电催化联合技术能够协同降解氯酚。 2-chlorophenol (2-CP) and 4-chlorophenol (4-CP) were treated respectively in .coupled ultrasound/electrocatalysis (US/EC) systems. The synergistic effects and influencing factors on chlorophenol decomposition were investigated. It was found that the removal efficiency was markedly higher in the coupled US/EC process than in the electrocatalysis process because of that the enhancement factors f were 1. 325 and 1. 509,respectively. The experimental results indicated that enhancement of current density could increase the removal efficiency of chlorophenol,the increment of apparent reaction rate constant were 1.28 ×10^-5s^-1 and 1.82 ×10^-5s^-1. High pH was advantageous to chlorophenol decomposition,apparent reaction rate constant were 9.22 ×10^-5s^-1 and 11.02×10^-5s^-1 at pH of 9.08. The decomposition efficiency of 2-CP increased more remarkably with the increase of electrolyte concentration than the one of 4-CP, the apparent reaction rate constant of 2-CP rose from 7.70 ×10^-5s^-1to 16.03 ×10^-5s^-1. In a word,chlorophenol could be decomposed in the synergistic US/EC process.
出处 《环境工程学报》 CAS CSCD 北大核心 2007年第1期45-49,共5页 Chinese Journal of Environmental Engineering
基金 浙江省科技厅重点资助项目(2005C23056)
关键词 声电联合氧化 电催化 超声波 氯酚 coupling ultrasound and electrocatalysis electrocatalysis ultrasound chlorophenol
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  • 1周明华,戴启洲,雷乐成,吴祖成,马淳安,汪大.新型二氧化铅阳极电催化降解有机污染物的特性研究[J].物理化学学报,2004,20(8):871-876. 被引量:61
  • 2陈延禧,夏晓霞,陈艳英,韩佐青.RuO_2-SnO_2电极的XPS研究与氧化物表面的酸碱性[J].化工学报,1995,46(5):586-592. 被引量:11
  • 3贾之慎,邬建敏,唐孟成.比色法测定Fenton反应产生的羟自由基[J].生物化学与生物物理进展,1996,23(2):184-186. 被引量:235
  • 4[1]Brzezinski B, Zundel G, 1996. Formation of hydrogen-bonded chains between a strong base with guanidine-like character and phenols with various pKa values an FT-IR study[J]. Mol Struct, 380(3): 195-204.
  • 5[2]De Visscher A, Van Langenhove H, 1998. Sonochemistry of organic compounds in homogeneous aqueous oxidizing systems[J]. Ultrason Sonochem, 5(3): 87-92.
  • 6[3]Drijvers D, Van Langenhove H, Vervaet K, 1998. Sonolysis of chlorobenzene in aqueous solution: organic intermediates[J]. Ultrason Sonochem, 5(1): 13-19.
  • 7[4]Entezari M H, Petrier C, Devidal P, 2003. Sonochemical degradation of phenol in water: a comparison of classical equipment with a new cylindrical reactor[J]. Ultrason Sonochem, 10(2): 103-108.
  • 8[5]Hua I, Hochemer R H, Hoffmann M R, 1995. Sonochemical degradation of p-nitrophenol in a parallel-plate near-field acoustical processor[J]. Environ Sci Technol, 29(11): 2790-2796.
  • 9[6]Ingale M N, Mahajani V V, 1995. A novel way to treat refractory waste:sonication followed by wet oxidation(SONIWO)[J]. Chem Tech Biotechnol, 64(1): 80-86.
  • 10[7]Jana A K, Chatterjee S N, 1995. Estimation of hydroxyl radicals produced by ultrasound in fricke solution used as a chemical dosimeter[J]. Ultrason Sonochem, 2(2): S87-S91.

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