Mechanism of oxidation and catalysis of organic matter abiotic humification in the presence of MnO2

被引:28
|
作者
Zhang, Yingchao [1 ]
Yue, Dongbei [1 ]
Wang, Xu [1 ]
Song, Wenfang [2 ]
机构
[1] Tsinghua Univ, Key Lab Solid Waste Management & Environm Safety, Sch Environm, Beijing 100084, Peoples R China
[2] Beijing Prod & Mkt Serv Stn Super Agr Prod, Beijing 100029, Peoples R China
来源
关键词
Abiotic humification; MnO2; Fulvic-like acids; Humic-like acids; CO2; release; HUMIC SUBSTANCES; FULVIC-ACIDS; STEEL SLAG; KINETICS; BINDING; CARBON;
D O I
10.1016/j.jes.2018.07.002
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Humification plays a critical role in the environmental fate of organic wastes, and MnO2 holds great promise for enhancing this reaction. However, the effects of MnO2 on the enhancement of the humification reaction remain ambiguous. To better reveal the mechanism by which MnO2 enhances the reaction and investigate the fate of the humification products, abiotic humification experiments were performed using increasing concentrations of dissolved organic matter (DOM) to a fixed amount of MnO2. DOM was represented by model humic precursors consisting of catechol, glucose and glycine. The results indicate that the reduction of MnO2 played a dominant role in the formation of fulvic-like acids (FLAs), and the subsequent reduction products, MnOOH and Mn(II), acted as catalysts in the formation of humic-like acids (HLAs). Moreover, CO2 release occurred during the formation of FLAs, and a strong linear correlation between CO2 release and the formation of FLAs was observed (p < 0.01), where 0.73-1.87 mg of CO2 was released per mg dissolved organic carbon (Doc) FLAs. Furthermore, the concentration of MnO2 had a pronounced influence on the product behavior, where a lower MnO2 concentration decreased the quantity of FLAs produced. (C) 2018 The Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences. Published by Elsevier B.V.
引用
收藏
页码:167 / 173
页数:7
相关论文
共 50 条
  • [41] Oxidation of As(III) by MnO2 in the absence and presence of Fe(II) under acidic conditions
    Han, Xu
    Li, Yi-Liang
    Gu, Ji-Dong
    GEOCHIMICA ET COSMOCHIMICA ACTA, 2011, 75 (02) : 368 - 379
  • [42] Surface structure effects in nanocrystal MnO2 and Ag/MnO2 catalytic oxidation of CO
    Xu, R
    Wang, X
    Wang, DS
    Zhou, KB
    Li, YD
    JOURNAL OF CATALYSIS, 2006, 237 (02) : 426 - 430
  • [43] Effect of MnO2 morphology on the catalytic oxidation of toluene over Ag/MnO2 catalysts
    Li, Jiamin
    Qu, Zhenping
    Qin, Yuan
    Wang, Hui
    APPLIED SURFACE SCIENCE, 2016, 385 : 234 - 240
  • [44] Oxidative reactivity of MnO2 in mixtures with FeIII oxides and/or natural organic matter (NOM)
    Zhang, Huichun
    Taujale, Saru
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2015, 249
  • [45] Electrodeposited MnO2 as electrocatalyst for carbohydrate oxidation
    Das, Debasmita
    Sen, Pratik Kumar
    Das, Kaushik
    JOURNAL OF APPLIED ELECTROCHEMISTRY, 2006, 36 (06) : 685 - 690
  • [46] Kinetics and mechanism of MnO2 dissolution in H2SO4 in the presence of pyrite
    B. B. Nayak
    K. G. Mishra
    R. K. Paramguru
    Journal of Applied Electrochemistry, 1999, 29 : 191 - 200
  • [47] Mechanism of the oxidation of d-glucose onto colloidal MnO2 surface in the absence and presence of TX-100 micelles
    Neelam Hazoor Kabir-ud-Din
    Mohd Zaidi
    Zaheer Akram
    Colloid and Polymer Science, 2006, 284 : 1387 - 1393
  • [48] Mechanism of the oxidation of D-glucose onto colloidal MnO2 surface in the absence and presence of TX-100 micelles
    Kabir-Ud-Din
    Zaidi, Neelam Hazoor
    Akram, Mohd
    Khan, Zaheer
    COLLOID AND POLYMER SCIENCE, 2006, 284 (12) : 1387 - 1393
  • [49] Kinetics and mechanism of MnO2 dissolution in H2SO4 in the presence of pyrite
    Nayak, BB
    Mishra, KG
    Paramguru, RK
    JOURNAL OF APPLIED ELECTROCHEMISTRY, 1999, 29 (02) : 191 - 200
  • [50] Electrodeposited MnO2 as electrocatalyst for carbohydrate oxidation
    Das, Debasmita
    Sen, Pratik Kumar
    Das, Kaushik
    Journal of Applied Electrochemistry, 2006, 36 (06): : 685 - 690