Suppr超能文献

[三价锰对水钠锰矿氧化三价铬的影响]

[Effects of Mn(III) on oxidation of Cr(III) with birnessites].

作者信息

Tan Jun-Feng, Qiu Guo-Hong, Liu Fan, Tan Wen-Feng, Feng Xiong-Han

机构信息

College of Resources and Environment, Huazhong Agricultural University, Wuhan 430070, China.

出版信息

Huan Jing Ke Xue. 2009 Sep 15;30(9):2779-85.

Abstract

Cr(III) could be oxidized only by manganese oxide minerals as natural inorganic oxidants in nature, and so the rate and mechanism of interaction between manganese oxide minerals and Cr(III) were widely concerned. The effects of Mn(III) in birnessites, the most common Mn oxide mineral in the environment, on the rate of Cr(III) oxidation with birnessites and the kinetic characteristics were investigated through batch kinetic technique. The results show that Cr(III) oxidation rate follows a pseudo-first-order reaction, and the apparent rate constant K(obs), is 0.031 3 min(-1) when the average oxidation state (AOS) of Mn is about 3.50 in birnessite. When the birnessite is pretreated with Na4P2O7 solution, and the Mn(III) can be complexed out from the solid oxides. Therefore the content of Mn(III) in the birnessites decreases and the AOS of manganese increases. The AOSs of Mn for the pretreated birnessites increase from 3.50 to 3.63, 3.73 and 3.78 when the concentrations of Na4P2O7 are about 10, 20 and 50 mmol/L respectively. The Mn(III) content does not affect the initial oxidation rate of Cr(III) markedly, although oxidation amount of Cr(III) increases with the AOS of Mn. The apparent rate constants for the corresponding pretreated birnessites are 0.035 1, 0.032 5 and 0.0309 min(-1) respectively. The oxidation rate of Cr( III) is markedly influenced by the amount of Mn(III) produced in the transformation process of Mn(VN) --> Mn(III). The newly formed Mn(III) is complexed by Na4P2O7 and the oxidation rate decreases to 45%-88%. The lower content of Mn(III) in birnessites, the more Mn(III) newly formed from the transformation of Mn(IV) is complexed out from the minerals, and the greater amplitude in the decrease of Cr(III) oxidation rate. Thus the newly formed Mn(III) is highly active and possesses fast rate of electron transfer, however the rate of electron transfer in the transformation process of Mn(IV) --> Mn(III) is relatively slow. It could be deduced that the controlling step of initial oxidation rate of Cr(III) with birnessites may be the electron transfer process of Mn(IV) --> Mn(III).

摘要

在自然界中,Cr(III)仅能被作为天然无机氧化剂的氧化锰矿物氧化,因此氧化锰矿物与Cr(III)之间相互作用的速率和机制受到广泛关注。通过间歇动力学技术研究了环境中最常见的氧化锰矿物水钠锰矿中Mn(III)对水钠锰矿氧化Cr(III)速率及动力学特征的影响。结果表明,Cr(III)的氧化速率符合准一级反应,当水钠锰矿中Mn的平均氧化态(AOS)约为3.50时,表观速率常数K(obs)为0.031 3 min⁻¹。用水解聚偏磷酸钠(Na4P2O7)溶液预处理水钠锰矿后,可使固体氧化物中的Mn(III)被络合出来,水钠锰矿中Mn(III)含量降低,Mn的氧化态升高。当Na4P2O7浓度分别约为10、20和50 mmol/L时,预处理后水钠锰矿的Mn氧化态分别从3.50升高到3.63、3.73和3.78。Mn(III)含量对Cr(III)的初始氧化速率影响不显著,尽管Cr(III)的氧化量随Mn的氧化态增加而增加。相应预处理水钠锰矿的表观速率常数分别为0.035 1、0.032 5和0.0309 min⁻¹。Cr(III)的氧化速率受Mn(VII)→Mn(III)转化过程中产生的Mn(III)量的显著影响。新形成的Mn(III)被Na4P2O7络合,氧化速率降低至45% - 88%。水钠锰矿中Mn(III)含量越低,由Mn(IV)转化新形成的Mn(III)从矿物中被络合出来的越多,Cr(III)氧化速率下降幅度越大。因此新形成的Mn(III)具有高活性且电子转移速率快,而Mn(IV)→Mn(III)转化过程中的电子转移速率相对较慢。可以推断,水钠锰矿氧化Cr(III)初始氧化速率的控制步骤可能是Mn(IV)→Mn(III)的电子转移过程。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验