Padhye Lokesh P
Department of Civil and Environmental Engineering, The University of Auckland, Auckland, New Zealand.
Department of Civil and Environmental Engineering, The University of Auckland, Auckland, New Zealand.
Chemosphere. 2017 Oct;184:532-547. doi: 10.1016/j.chemosphere.2017.06.021. Epub 2017 Jun 7.
Inorganic nitrogen contaminants (INC) (NH, NO, NO, NH, NO, NO, and NO) pose a growing risk to the environment, and their remediation methods are highly sought after. Application of carbon materials (CM), such as biochar and activated carbon, to remediate INC from agricultural fields and wastewater treatment plants has gained a significant interest since past few years. Understanding the role of surface chemistry of CM in adsorption of various INC is highly critical to increase adsorption efficiency as well as to assess the long term impact of using these highly recalcitrant CM for remediation of INC. Critical reviews of adsorption studies related to INC have revealed that carbon surface chemistry (surface functional groups, pH, Eh, elemental composition, and mineral content) has significant influence on adsorption of INC. Compared to basic functional groups, oxygen containing surface functional groups have been found to be more influential for adsorption of INC. However, basic sites on carbon materials still play an important role in chemisorption of anionic INC. Apart from surface functional groups, pH, Eh and pH of CM and elemental and mineral composition of its surface are important properties capable of altering INC interactions with CM. This review summarizes our current understanding of INC interactions with CM's surface through the known chemisorption mechanisms: electrostatic interaction, hydrogen bonding, electron donor-acceptor mechanism, hydrophobic and hydrophilic interaction, chemisorption aided by minerals, and interactions influenced by pH and elemental composition. Change in surface chemistry of CM in soil during aging is also discussed.
无机氮污染物(INC)(NH₃、NO₃⁻、NO₂⁻、NH₄⁺、NO₂、NO₃⁻和N₂O)对环境构成的风险日益增加,因此其修复方法备受关注。自过去几年以来,生物炭和活性炭等碳材料(CM)在修复农田和污水处理厂中的无机氮污染物方面的应用受到了广泛关注。了解碳材料表面化学在各种无机氮污染物吸附中的作用对于提高吸附效率以及评估使用这些高度难降解的碳材料修复无机氮污染物的长期影响至关重要。对与无机氮污染物相关的吸附研究的批判性综述表明,碳表面化学(表面官能团、pH值、氧化还原电位、元素组成和矿物质含量)对无机氮污染物的吸附有显著影响。与碱性官能团相比,含氧化合物表面官能团对无机氮污染物的吸附更具影响力。然而,碳材料上的碱性位点在阴离子无机氮污染物的化学吸附中仍然起着重要作用。除了表面官能团外,碳材料的pH值、氧化还原电位以及其表面的元素和矿物质组成也是能够改变无机氮污染物与碳材料相互作用的重要性质。本综述通过已知的化学吸附机制总结了我们目前对无机氮污染物与碳材料表面相互作用的理解:静电相互作用、氢键、电子供体-受体机制、疏水和亲水相互作用、矿物辅助化学吸附以及受pH值和元素组成影响的相互作用。还讨论了老化过程中土壤中碳材料表面化学的变化。