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水体系中亚铁离子与六方水钠锰矿的相互作用机制及动力学

Interaction mechanisms and kinetics of ferrous ion and hexagonal birnessite in aqueous systems.

作者信息

Gao Tianyu, Shen Yougang, Jia Zhaoheng, Qiu Guohong, Liu Fan, Zhang Yashan, Feng Xionghan, Cai Chongfa

机构信息

Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtse River), Ministry of Agriculture, College of Resources and Environment, Huazhong Agricultural University, Wuhan, 430070 People's Republic of China.

Department of Chemistry, University of Connecticut, Storrs, 55 North Eagleville Road, Storrs, CT 06269 USA.

出版信息

Geochem Trans. 2015 Sep 22;16(1):16. doi: 10.1186/s12932-015-0031-3. eCollection 2015 Dec.

Abstract

BACKGROUND

In soils and sediments, manganese oxides and oxygen usually participate in the oxidation of ferrous ions. There is limited information concerning the interaction process and mechanisms of ferrous ions and manganese oxides. The influence of air (oxygen) on reaction process and kinetics has been seldom studied. Because redox reactions usually occur in open systems, the participation of air needs to be further investigated.

RESULTS

To simulate this process, hexagonal birnessite was prepared and used to oxidize ferrous ions in anoxic and aerobic aqueous systems. The influence of pH, concentration, temperature, and presence of air (oxygen) on the redox rate was studied. The redox reaction of birnessite and ferrous ions was accompanied by the release of Mn and K ions, a significant decrease in Fe concentration, and the formation of mixed lepidocrocite and goethite during the initial stage. Lepidocrocite did not completely transform into goethite under anoxic condition with pH about 5.5 within 30 days. Fe exhibited much higher catalytic activity than Mn during the transformation from amorphous Fe(III)-hydroxide to lepidocrocite and goethite under anoxic conditions. The release rates of Mn were compared to estimate the redox rates of birnessite and Fe under different conditions.

CONCLUSIONS

Redox rate was found to be controlled by chemical reaction, and increased with increasing Fe concentration, pH, and temperature. The formation of ferric (hydr)oxides precipitate inhibited the further reduction of birnessite. The presence of air accelerated the oxidation of Fe to ferric oxides and facilitated the chemical stability of birnessite, which was not completely reduced and dissolved after 18 days. As for the oxidation of aqueous ferrous ions by oxygen in air, low and high pHs facilitated the formation of goethite and lepidocrocite, respectively. The experimental results illustrated the single and combined effects of manganese oxide and air on the transformation of Fe to ferric oxides. Graphical abstract:Lepidocrocite and goethite were formed during the interaction of ferrous ion and birnessite at pH 4-7. Redox rate was controlled by the adsorption of Fe2+ on the surface of birnessite. The presence of air (oxygen) accelerated the oxidation of Fe2+ to ferric oxides and facilitated the chemical stability of birnessite.

摘要

背景

在土壤和沉积物中,锰氧化物和氧气通常参与亚铁离子的氧化过程。关于亚铁离子与锰氧化物相互作用的过程和机制的信息有限。空气(氧气)对反应过程和动力学的影响鲜有研究。由于氧化还原反应通常发生在开放体系中,空气的参与情况需要进一步研究。

结果

为模拟该过程,制备了六方水钠锰矿并用于在缺氧和好氧水体系中氧化亚铁离子。研究了pH值、浓度、温度以及空气(氧气)的存在对氧化还原速率的影响。水钠锰矿与亚铁离子的氧化还原反应伴随着锰和钾离子的释放、铁浓度的显著降低,以及在初始阶段混合纤铁矿和针铁矿的形成。在pH约为5.5的缺氧条件下,30天内纤铁矿没有完全转化为针铁矿。在缺氧条件下,从无定形氢氧化铁(III)转化为纤铁矿和针铁矿的过程中,铁表现出比锰更高的催化活性。比较了锰的释放速率以估计不同条件下水钠锰矿和铁的氧化还原速率。

结论

发现氧化还原速率受化学反应控制,并随铁浓度、pH值和温度的升高而增加。铁(氢)氧化物沉淀的形成抑制了水钠锰矿的进一步还原。空气的存在加速了铁氧化为铁氧化物,并促进了水钠锰矿的化学稳定性,18天后水钠锰矿没有完全还原和溶解。至于空气中的氧气对水溶液中亚铁离子的氧化作用,低pH值和高pH值分别促进了针铁矿和纤铁矿的形成。实验结果说明了氧化锰和空气对铁转化为铁氧化物的单一和综合影响。图形摘要:在pH值为4 - 7时,亚铁离子与水钠锰矿相互作用过程中形成了纤铁矿和针铁矿。氧化还原速率受Fe2+在水钠锰矿表面的吸附控制。空气(氧气)的存在加速了Fe2+氧化为铁氧化物,并促进了水钠锰矿的化学稳定性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c25e/4607026/24262ae668f7/12932_2015_31_Figa_HTML.jpg

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