US/Zn0体系降解水中的对硝基苯甲酸

宋亚丽, 张光明, 常爱敏, 王丽, 宗栋良. US/Zn0体系降解水中的对硝基苯甲酸[J]. 环境工程学报, 2014, 8(5): 1797-1801.
引用本文: 宋亚丽, 张光明, 常爱敏, 王丽, 宗栋良. US/Zn0体系降解水中的对硝基苯甲酸[J]. 环境工程学报, 2014, 8(5): 1797-1801.
Song Yali, Zhang Guangming, Chang Aimin, Wang Li, Zong Dongliang. Degradation of p-nitrobenzoic acid by US/Zn0 system[J]. Chinese Journal of Environmental Engineering, 2014, 8(5): 1797-1801.
Citation: Song Yali, Zhang Guangming, Chang Aimin, Wang Li, Zong Dongliang. Degradation of p-nitrobenzoic acid by US/Zn0 system[J]. Chinese Journal of Environmental Engineering, 2014, 8(5): 1797-1801.

US/Zn0体系降解水中的对硝基苯甲酸

  • 基金项目:

    深圳市科技研发资金项目(JSF201006300042A)

    国家自然科学基金资助项目(51278489)

  • 中图分类号: X703

Degradation of p-nitrobenzoic acid by US/Zn0 system

  • Fund Project:
  • 摘要: 为高效去除水体中的对硝基苯甲酸、开发新型水处理技术,提出以超声与单质锌联用降解水中的对硝基苯甲酸。考察了锌投加量、溶液初始pH、声功率及溶液初始浓度对拟一级反应速率常数(kUS/Zn0)的影响,比较了US、Zn0和US/Zn0 3体系下的降解常数,并对US/Zn0体系的降解机理进行了初探。结果表明,以上4种因素对kUS/Zn0均有很大影响,kUS/Zn0分别在溶液初始pH为5、声功率为120 W、溶液初始浓度为0.04 mmol/L时达到最大值,且随着锌投加量的增加而增加。超声与单质锌在降解对硝基苯甲酸的过程中存在很好的协同作用,在最优条件下,kUS/Zn0=0.052 min-1,分别是单独超声降解及单独锌降解的21.5倍和2.53倍。在联用体系中,主要是依靠OH·氧化及单质锌还原的相互加强来去除对硝基苯甲酸。
  • 加载中
  • [1] 吴双桃, 陈少瑾, 胡劲召, 等. 零价铁对土壤中硝基苯类化合物的还原作用. 中国环境科学, 2005, 25(2):188-191 Wu Shuangtao, Chen Shaojin, Hui Jinzhao, et al. Reduction action of zero-valent iron on nitrobenzene compounds in soils. China Environmental Science, 2005, 25(2):188-191 (in Chinese)
    [2] Yean Ling Pang, Ahmad Zuhairi Abdullah, Subhash Bhatia. Review on sonochemical methods in the presence of catalysts and chemical additives for treatment of organic pollutants in wastewater.Desalination, 2011, 277(1-3):1-14
    [3] 陈宜菲, 陈少瑾.利用零价铁还原土壤中硝基苯类化合物的研究.环境科学学报, 2007, 27(2):241-246 Chen Yifei, Chen Shaojin.Reduction of nitrobenzenes in soils by zero valent iron.Acta Scientiae Circumstantiae, 2007, 27(2):241-246 (in Chinese)
    [4] Thirugnanasambandam Sivasankar, Vijayanand S. Moholkar. Physical features of sonochemical degradation of nitroaromatic pollutants. Chemosphere, 2008, 72(11): 1795-1806
    [5] Amey A. Pradhan, Parag R. Gogate. Degradation of p-nitrophenol using acoustic cavitation and Fenton chemistry. Journal of Hazardous Materials, 2010, 173(1-3):517-522
    [6] 郭照冰, 郑正, 胡文勇, 等. 2, 4-二硝基酚的超声波及协同降解研究. 环境科学学报, 2004, 24(2):237-241 Guo Zhaobing, Zheng Zheng, Hu Wenyong, et al. Study on degradation of 2, 4-dinitrophenol by ultrasonic-wave and synergic system. Acta Scientiae Circumstantiae, 2004, 24(2): 237-241 (in Chinese)
    [7] 郭中权, 周如禄, 高亮.臭氧催化氧化处理对硝基苯甲酸废水.能源环境保护, 2004, 18(5):39-41 Guo Zhongquan, Zhou Lu, Gao Liang. Treatment of paranitrobenzoic acid wastewater by micro-electrolyzation and O3 catalysis-oxidation.Energy Envirenmental Protection, 2004, 18(5): 39-41 (in Chinese)
    [8] 孙育平, 徐丹, 孙杰, 等.可见光照FePz (dtnCl2)4活化过氧化氢降解对硝基苯甲酸.武汉大学学报(理学版), 2007, 53(4):401-404 Sun Yuping, Xu Ping, Sun Jie, et al. Photodegradation of 4-nitrobenzoic acid by hydrogen peroxide in the presence of FePz (dtnCl2)4 under visible irradiation. Journal of Wuhan University (Nat. Sci. Ed.), 2007, 53(4): 401-404 (in Chinese)
    [9] 钱国铢, 赵金金, 朱昱, 等.银纳米粒子上对硝基苯甲酸的催化还原.光谱实验室, 2007, 24(4):643-645 Qian Guozhu, Zhao Jinjin, Zhu Yu, et al. Catalatic reduction of p-nitrobenzoic acid by silver nanoparticles. Chinese Journal of Spectroscopy Laboratory, 2007, 24(4): 643-645(in Chinese)
    [10] Pankaj Chowdhury, Viraraghavan T. Sonochemical degradation of chlorinated organic compounds, phenolic compounds and organic dyes:A review. Science of the Total Environment, 2009, 407(8):2474-2492
    [11] Ince N. H., Tezcanli G., Belen R. K., et al. Ultrasound as a catalyzer of aqueous reaction systems:The state of the art and environmental applications. Applied Catalysis B:Environmental, 2001, 29 (3):167-176
    [12] Youzhi Dai, Fenfang Li, Fei Ge, et al. Mechanism of the enhanced degradation of pentachlorophenol by ultrasound in the presence of elemental iron. Journal of Hazardous Materials, 2006, 137 (3):1424-1429
    [13] 陈忠林, 韩莹, 杨磊, 等.零价锌还原水中痕量亚硝基二甲胺的效能.哈尔滨工业大学学报, 2010, 42(12):1879-1882 Chen Zhonglin, Han Ying, Yang Lei, et al. Efficiency of reduction of trace nitrosodimethylamine(NDMA) in water by zero-valent zinc. Journal of Harbin Institute of Technology, 2010, 42(12):1879-1882 (in Chinese)
    [14] Joost Rooze, Evgeny V. Rebrov, Jaap C.Schouten, et al. Dissolved gas and ultrasonic cavitation:A review. Ultrasonic Sonochemistry, 2013, 20(1):1-11
    [15] Gertraud Mark, Armin Tauber, Rudiger Laupert, et al. OH· radical formation by ultrasound in aqueous solution-part Ⅱ:Terephthalate and Fricke dosimetry and the influence of various conditions on the sonolytic yield. Ultrasonics Sonochemistry, 1988, 5(2):41-52
    [16] Kashyap P. Mishra, Parag R. Gogate. Intensification of sonophotocatalytic degradation of p-nitrophenol at pilot scale capacity. Ultrasonics Sonochemistry, 2011, 18(3):739-744
    [17] R.D. Holstvoogd, W.P.M. van Swaaij, L.L. van Dierendonck. The absorption of gases in aqueous activated carbon slurries enhanced by adsorbing or catalytic particles. Chemical Engineering Science, 1988, 43(8):2181-2187
  • 加载中
计量
  • 文章访问数:  1762
  • HTML全文浏览数:  984
  • PDF下载数:  898
  • 施引文献:  0
出版历程
  • 收稿日期:  2013-05-07
  • 刊出日期:  2014-05-06
宋亚丽, 张光明, 常爱敏, 王丽, 宗栋良. US/Zn0体系降解水中的对硝基苯甲酸[J]. 环境工程学报, 2014, 8(5): 1797-1801.
引用本文: 宋亚丽, 张光明, 常爱敏, 王丽, 宗栋良. US/Zn0体系降解水中的对硝基苯甲酸[J]. 环境工程学报, 2014, 8(5): 1797-1801.
Song Yali, Zhang Guangming, Chang Aimin, Wang Li, Zong Dongliang. Degradation of p-nitrobenzoic acid by US/Zn0 system[J]. Chinese Journal of Environmental Engineering, 2014, 8(5): 1797-1801.
Citation: Song Yali, Zhang Guangming, Chang Aimin, Wang Li, Zong Dongliang. Degradation of p-nitrobenzoic acid by US/Zn0 system[J]. Chinese Journal of Environmental Engineering, 2014, 8(5): 1797-1801.

US/Zn0体系降解水中的对硝基苯甲酸

  • 1. 哈尔滨工业大学市政环境工程学院, 哈尔滨 150090
  • 2. 中国人民大学环境学院, 北京 100872
  • 3. 深圳市水质检测中心, 深圳 440300
基金项目:

深圳市科技研发资金项目(JSF201006300042A)

国家自然科学基金资助项目(51278489)

摘要: 为高效去除水体中的对硝基苯甲酸、开发新型水处理技术,提出以超声与单质锌联用降解水中的对硝基苯甲酸。考察了锌投加量、溶液初始pH、声功率及溶液初始浓度对拟一级反应速率常数(kUS/Zn0)的影响,比较了US、Zn0和US/Zn0 3体系下的降解常数,并对US/Zn0体系的降解机理进行了初探。结果表明,以上4种因素对kUS/Zn0均有很大影响,kUS/Zn0分别在溶液初始pH为5、声功率为120 W、溶液初始浓度为0.04 mmol/L时达到最大值,且随着锌投加量的增加而增加。超声与单质锌在降解对硝基苯甲酸的过程中存在很好的协同作用,在最优条件下,kUS/Zn0=0.052 min-1,分别是单独超声降解及单独锌降解的21.5倍和2.53倍。在联用体系中,主要是依靠OH·氧化及单质锌还原的相互加强来去除对硝基苯甲酸。

English Abstract

参考文献 (17)

返回顶部

目录

/

返回文章
返回