pH对不同来源溶解性有机质光致生成活性物种量子产率的影响

马哲, 王杰琼, 陈景文, 乔显亮, 李雪花, 蔡喜运. pH对不同来源溶解性有机质光致生成活性物种量子产率的影响[J]. 环境化学, 2017, 36(9): 1889-1895. doi: 10.7524/j.issn.0254-6108.2017012301
引用本文: 马哲, 王杰琼, 陈景文, 乔显亮, 李雪花, 蔡喜运. pH对不同来源溶解性有机质光致生成活性物种量子产率的影响[J]. 环境化学, 2017, 36(9): 1889-1895. doi: 10.7524/j.issn.0254-6108.2017012301
MA Zhe, WANG Jieqiong, CHEN Jingwen, QIAO Xianliang, LI Xuehua, CAI Xiyun. Effect of pH on the quantum yield of reactive photo-induced species generated in different sources of DOM[J]. Environmental Chemistry, 2017, 36(9): 1889-1895. doi: 10.7524/j.issn.0254-6108.2017012301
Citation: MA Zhe, WANG Jieqiong, CHEN Jingwen, QIAO Xianliang, LI Xuehua, CAI Xiyun. Effect of pH on the quantum yield of reactive photo-induced species generated in different sources of DOM[J]. Environmental Chemistry, 2017, 36(9): 1889-1895. doi: 10.7524/j.issn.0254-6108.2017012301

pH对不同来源溶解性有机质光致生成活性物种量子产率的影响

  • 基金项目:

    国家重点基金研究计划(973计划)课题(2013CB430403)资助.

Effect of pH on the quantum yield of reactive photo-induced species generated in different sources of DOM

  • Fund Project: Supported by the National Basic Research Program of China (2013CB430403).
  • 摘要: 溶解性有机质(DOM)普遍存在于地表水中,DOM吸收太阳光可生成多种光致活性物种(RPS),如激发三线态DOM (3DOM*)、单线态氧(1O2)和羟基自由基(·OH)等.这些RPS对污染物的降解具有重要作用.天然水pH改变可导致DOM的粒径、官能团和分子量等变化,但pH对DOM生成RPS的影响少有研究.本文在模拟日光条件下,采用分子探针的方法测定了提取的黄海海水DOM (L-DOM)和两种购于国际腐殖酸协会的DOM (NAFA和SRHA)在pH值为4.0、7.0和9.0条件下生成3DOM*,1O2和·OH的量子产率.结果表明,3种DOM均可光致生成RPS,L-DOM生成RPS的量子产率远高于SRHA和NAFA.pH对不同来源DOM生成RPS的量子产率的影响不同,其中对L-DOM的影响最为显著.本研究有助于揭示水中有机污染物的光化学转化动力学.
  • 加载中
  • [1] ROCHELLE-NEWA E J, FISHER T R. Chromophoric dissolved organic matter and dissolved organic carbon in Chesapeake Bay[J]. Marine Chemistry, 2002, 77(1):23-41.
    [2] COBLE P G. Marine optical biogeochemistry:The chemistry of ocean color[J]. Chemical Reviews, 2007, 107(2):402-418.
    [3] SANCHES S, LEITAO C, PENETRA A, et al. Direct photolysis of polycyclic aromatic hydrocarbons in drinking water sources[J]. Journal of Hazardous Materials, 2011, 192(3):1458-1465.
    [4] JUANG J, KIM J K, JEONG D H, et al. Environmental levels of ultraviolet light potentiate the toxicity of sulfonamide antibiotics in Daphnia magna[J]. Ecotoxicology, 2008, 17(1):37-45.
    [5] MILLER P L, CHIN Y P. Indirect photolysis promoted by natural and engineered wetland water constituents:Processes leading to alachlor degradation[J]. Environmental Science and Technology, 2005, 39(12):4454-4462.
    [6] GE L K, CHEN J W, QIAO X L, et al. Light-source-dependent effects of main water constituents on photodegradation of phenicol antibiotics:Mechanism and kinetics[J]. Environmental Science and Technology, 2009, 43(9):3101-3107.
    [7] PAN B, GHOSH S, XING B S. Dissolved organic matter conformation and its interaction with pyrene as affected by water chemistry and concentration[J]. Environmental Science and Technology, 2008, 42(5):1594-1599.
    [8] GAO Y, YAN M Q, KORSHIN G V. Effects of ionic strength on the chromophores of dissolved organic matter[J]. Environmental Science and Technology, 2015, 49(10):5905-5912.
    [9] KROP H B, VAN NOORT P C M, GOVERS H A J. Determination and theoretical aspects of the equilibrium between dissolved organic matter and hydrophobic organic micropollutants in water (Kdoc)[J]. Reviews of Environmental Contamination and Toxicology, 2001, 169(1):1-122.
    [10] LEE E, GLOVER C M, ROSARIO-ORTIZ F L. Photochemical formation of hydroxyl radical from effluent organic matter:Role of composition[J]. Environmental Science and Technology, 2013. 47(1):12073-12080.
    [11] GLOVER C M, ROSARIO-ORTIZ F L. Impact of halides on the photoproduction of reactive intermediates from organic matter[J]. Environmental Science and Technology, 2013, 47(24):13949-13956.
    [12] LAURENTⅡS E D, BUOSO S B, MAURINO V, et al. Optical and photochemical characterization of chromophoric dissolved organic matter from lakes in Terra Nova Bay, Antarctica. Evidence of considerable photoreactivity in an extreme environment[J]. Environmental Science and Technology, 2013, 47(24):14089-14098.
    [13] 王杰琼, 乔显亮, 张耀玲, 等. 采用电渗析耦合反渗透法分离养殖海水中溶解性有机质[J]. 环境化学, 2016, 35(9):1785-1791.

    WANG J Q, QIAO X L, ZHANG Y L, et al. Isolation of dissolved organic matter from mariculture seawaters by electrodialysis coupled with reverse osmosis[J]. Environmental Chemistry, 2016, 35(9):1785-1791(in Chinese).

    [14] HALLADIA S, TER HALLE A, AGUER J P, et al. Inhibition of humic substances mediates photooxygenation of furfuryl alcohol by 2,4,6-trimethylphenol. Evidence for reactivity of the phenol with humic triplet excited states[J]. Environmental Science and Technology, 2007, 41(17):6066-6073.
    [15] DE L E, MINELLA M, MAURINO V, et al. Photochemical production of organic matter triplet states in water samples from mountain lakes, located below or above the tree line[J]. Chemosphere, 2012, 88(10):1208-1213.
    [16] HAAG W R, HOIGNE J, GASSMAN E, et al. Singlet oxygen in surface waters-Part Ⅰ:Furfuryl alcohol as a trapping agent[J]. Chemosphere, 1984, 13(5-6):631-640.
    [17] BURNS J M, COOPER W J, FERRY J L, et al. Methods for reactive oxygen species (ROS) detection in aqueous environments[J]. Aquatic Sciences, 2012, 74(4):683-734.
    [18] BUXTON G V, GREENSTOCK C L, HELMAN W P, et al. Critical review of rate constants for reactions of hydrated electrons, hydrogen atoms and hydroxyl radicals (·OH/·O-) in aqueous solution[J]. Journal of Physical and Chemical Reference Data, 1988, 17(2):1027-1284.
    [19] VIONE D, FALLETTI G, MAURINO V, et al. Sources and sinks of hydroxyl radicals upon irradiation of natural water samples[J]. Environmental Science and Technology, 2006, 40(12):3775-3781.
    [20] PEURAVUORI J, PIHLAJA K. Molecular size distribution and spectroscopic properties of aquatic humic substances[J]. Analytica Chimica Acta, 1997, 33(2):133-149.
    [21] TREMBLAY L B, DITTMAR T, MARSHALL A G, et al. Molecular characterization of dissolved organic matter in a north Brazilian mangrove porewater and mangrove-fringed estuaries by ultrahigh resolution fourier transform-ion cyclotron resonance mass spectrometry and excitation/emission spectroscopy[J]. Marine Chemistry, 2007, 105(1-2):15-29.
    [22] LANDRY C, TREMBLAY L. Compositional differences between size classes of dissolved organic matter from freshwater and seawater revealed by an HPLC-FTIR system[J]. Environment Science and Technology, 2012, 46(3):1700-1707.
    [23] DALRYMPLE R M, CARFAGNO A K, SHARPLESS C M. Correlation between dissolved organic matter optical properties and quantum yields of singlet oxygen and hydrogen peroxide[J]. Environment Science and Technology, 2010, 44(15):5824-5829.
    [24] BODHIPAKSHA L C, SHARPLESS C M, CHIN Y P, et al. Triplet photochemistry of effluent and natural organic matter in whole water and isolates from effluent-receiving rivers[J]. Environment Science and Technology, 2015, 49(6):3453-3463.
    [25] HANSELL D A, CARLANO C A. Deep-ocean gradients in the concentration of dissolved organic carbon[J]. Nature, 1998, 395(6699):263-266.
    [26] PETERSON B M, MC NALLY A M, CORY R M, et al. Spatial and temporal distribution of singlet oxygen in Lake Superior[J]. Environmental Science and Technology, 2012, 46(13):7222-7229.
    [27] HALPERN B S, SELKOE K A, MICHELI F, et al. Evaluating and ranking the vulnerability of global marine ecosystems to anthropogenic threats[J]. Conservation Biology, 2007, 21(5):1301-1315.
    [28] MOSTAFA S, ROSARIO-ORTIZ F L. Singlet oxygen formation from wastewater organic matter[J]. Environmental Science and Technology, 2013, 47(15):8179-8186.
  • 加载中
计量
  • 文章访问数:  1708
  • HTML全文浏览数:  1594
  • PDF下载数:  237
  • 施引文献:  0
出版历程
  • 收稿日期:  2017-01-23
  • 刊出日期:  2017-09-15
马哲, 王杰琼, 陈景文, 乔显亮, 李雪花, 蔡喜运. pH对不同来源溶解性有机质光致生成活性物种量子产率的影响[J]. 环境化学, 2017, 36(9): 1889-1895. doi: 10.7524/j.issn.0254-6108.2017012301
引用本文: 马哲, 王杰琼, 陈景文, 乔显亮, 李雪花, 蔡喜运. pH对不同来源溶解性有机质光致生成活性物种量子产率的影响[J]. 环境化学, 2017, 36(9): 1889-1895. doi: 10.7524/j.issn.0254-6108.2017012301
MA Zhe, WANG Jieqiong, CHEN Jingwen, QIAO Xianliang, LI Xuehua, CAI Xiyun. Effect of pH on the quantum yield of reactive photo-induced species generated in different sources of DOM[J]. Environmental Chemistry, 2017, 36(9): 1889-1895. doi: 10.7524/j.issn.0254-6108.2017012301
Citation: MA Zhe, WANG Jieqiong, CHEN Jingwen, QIAO Xianliang, LI Xuehua, CAI Xiyun. Effect of pH on the quantum yield of reactive photo-induced species generated in different sources of DOM[J]. Environmental Chemistry, 2017, 36(9): 1889-1895. doi: 10.7524/j.issn.0254-6108.2017012301

pH对不同来源溶解性有机质光致生成活性物种量子产率的影响

  • 1. 大连理工大学环境学院, 工业生态与环境工程教育部重点实验室, 大连, 116024
基金项目:

国家重点基金研究计划(973计划)课题(2013CB430403)资助.

摘要: 溶解性有机质(DOM)普遍存在于地表水中,DOM吸收太阳光可生成多种光致活性物种(RPS),如激发三线态DOM (3DOM*)、单线态氧(1O2)和羟基自由基(·OH)等.这些RPS对污染物的降解具有重要作用.天然水pH改变可导致DOM的粒径、官能团和分子量等变化,但pH对DOM生成RPS的影响少有研究.本文在模拟日光条件下,采用分子探针的方法测定了提取的黄海海水DOM (L-DOM)和两种购于国际腐殖酸协会的DOM (NAFA和SRHA)在pH值为4.0、7.0和9.0条件下生成3DOM*,1O2和·OH的量子产率.结果表明,3种DOM均可光致生成RPS,L-DOM生成RPS的量子产率远高于SRHA和NAFA.pH对不同来源DOM生成RPS的量子产率的影响不同,其中对L-DOM的影响最为显著.本研究有助于揭示水中有机污染物的光化学转化动力学.

English Abstract

参考文献 (28)

返回顶部

目录

/

返回文章
返回