mn oxides
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Fuel ◽  
2022 ◽  
Vol 310 ◽  
pp. 122237
Author(s):  
Aidong Fan ◽  
Yue Jing ◽  
Jiaxiu Guo ◽  
Xueke Shi ◽  
Shandong Yuan ◽  
...  
Keyword(s):  
Nh3 Scr ◽  
Mn Doped ◽  

2022 ◽  
Vol 520 ◽  
pp. 230868
Author(s):  
Chuangxin Ge ◽  
Qihao Li ◽  
Meixue Hu ◽  
Gongwei Wang ◽  
Li Xiao ◽  
...  

2022 ◽  
pp. 100106
Author(s):  
Shanhong Wan ◽  
Yifan Li ◽  
Lijin Xu ◽  
Wei Zhang ◽  
Rui Cao

Chemosphere ◽  
2021 ◽  
pp. 133442
Author(s):  
Ji Mei ◽  
Yao Shen ◽  
Yuanming Li ◽  
Shihan Zhang ◽  
Yi Shen ◽  
...  
Keyword(s):  

Catalysts ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 1437
Author(s):  
Ewelina Ksepko ◽  
Rafal Lysowski

The objective of the research was to prepare Mn-based materials for use as oxygen carriers and investigate their reactivity in terms of their applicability to energy systems. The family of Fe2O3-MnO2 with the addition of TiO2 was prepared by mechanical mixing method and calcination. Five samples with addition of Fe2O3 (20, 30, 35, and 50 wt.%) to MnO2 (65, 55, 50, 35, and 85 wt.%) with constant amount of inert TiO2 (15 wt.%) were prepared. The performance of TiO2 supported Fe-Mn oxides oxygen carriers with hydrogen/air in an innovative combustion technology known as chemical looping combustion (CLC) was evaluated. Thermogravimetric analysis was used for reactivity studies within a wide temperature range (800–1000 °C). Comprehensive characterization contained multipurpose techniques for newly synthesized materials. Moreover, post-reaction experiments considered morphology analysis by SEM, mechanical strength testing by dynamometry, and crystal phase study by XRD. Based on wide-ranging testing, the F50M35 sample was indicated as the most promising for gaseous fuel combustion via CLC at 850–900 °C temperature.


Author(s):  
Wang Wang ◽  
Ershuai Liu ◽  
Youcheng Hu ◽  
Li Jiao ◽  
Praveen Kolla ◽  
...  
Keyword(s):  

2021 ◽  
Author(s):  
Lin Deng ◽  
Jiangxia Wang ◽  
Bin Xu ◽  
Xiaoting Yang ◽  
Anyan Hu

Abstract In this study, distributing characteristics of five fluorine (F) species in loess in the Shaanxi Loess Plateau (SLP) were determined including unextractable residual F (Fre), extractable water-soluble F (Fws), exchangeable F (Fex), F bound to Fe-Mn oxides (Ffm), and F bound to organics (For). The results show that unextractable Fre represents most percentage of Ftf in loess. Of the four extractable F species, the content of Fws is higher than the other three extractable F species in most loess samples. The loess in the southeast SLP has the highest Fws content while the loess in the southwest has the highest Ftf content. And the loess in the north SLP contains the lowest overall concentrations of Ftf and Fws. Similar to Fws, the respective content of Fex, Ffm, and For in the loess is also very low. However, the total of them and Fws cannot be negligible for F mobility in loess. Overall, the loess in the SLP can be assessed as inferior quality in terms of F as a result of high Fws content in most samples. Based on the F speciation in the loess, F exposure to grazing animals and humans, in fact to children, was assessed, indicating that F in the loess in the southwest SLP might pose a much greater risk to grazing animals than in other part of SLP as the loess contains more Ftf. However, there is no concern for the children’s exposure to loess F via ingestion in the study area in the present condition. As for the loess F risk to groundwater, it can be concluded that not only Fws but also the other extractable F including Fex, Ffm and For in loess may be responsible for the F enrichment in local groundwater in the area with the aid of the characteristics of F speciation in loess and distribution of local high-fluoride groundwater.


Minerals ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 1168
Author(s):  
Nastja Rogan Šmuc ◽  
Nives Kovač ◽  
Žan Hauptman ◽  
Andrej Šmuc ◽  
Matej Dolenec ◽  
...  

Hypersaline environments are among the most vulnerable coastal ecosystems and are extremely noteworthy for a variety of ecological reasons. Comprehensive assessment of metal(oid) contamination in hypersaline sediments from Sečovlje (Northern Adriatic, Slovenia) was addressed by introducing the detrital and diagenetic mineralogy and geochemical properties within the solid sediment material. Close associations between Fe/Mn oxides and oxyhydroxides with As, Cr, Ni, Pb and Zn, and between organic matter with Cu, Pb and Zn were confirmed using X-ray powder diffraction, SEM-EDS and ICP emission spectrometry analysis. Possible incorporation or adsorption on the crystal lattices of clay minerals (As, Cr, Pb, Sn and Zn), halite (As) and aragonite/calcite (Cd, Cu, Pb, Sr and Zn) were also detected. All presented correlations were highlighted by various statistical analyses. The enrichment factor (EF) values showed a low degree of anthropogenic burden for As, Bi, Hg and Zn, while Cd, Cr, Cu, Ni, Pb, Sn and Sr originated from the geological background. These results emphasise that a detailed mineralogical and geochemical characterisation of solid (especially detrital and diagenetic) sediment particles is crucial in further understanding the metal(oid) translocation within the hypersaline ecosystems.


2021 ◽  
Author(s):  
Sha Chen ◽  
Zhexu Ding ◽  
Jinyuan Chen ◽  
Jun Luo ◽  
Xiaofang Ruan ◽  
...  

Abstract Bacterial non-enzymatic Mn(II) oxidation involving reactive oxygen species (ROS) (i.e. indirect oxidation), initially discovered from a marine alpha-proteobacterium, is believed to be of importance in controlling biogeochemical cycles. For soil-borne bacteria, however, evidence of indirect Mn(II) oxidation remains unclear. In this study, the indirect Mn(II) oxidation was evidenced in a soil-borne bacterium, Providencia sp. LLDRA6. First, with and without 50 mM of Mn(II) exposure for LLDRA6, 300 differentially expressed genes were found to be linked to Mn(II) exposure via transcriptome sequencing. Among them, an operon, responsible for phenylacetic acid catabolism, was sharply upregulated in transcription, drawing us a special attention since its transcriptional upregulation has recently shown to be important for withstanding ROS. Next, a fluorometric probe, 2′,7′-Dichlorofluorescin diacetate (DCFDA), was used to qualitatively detect ROS from cells, showing a distinct increase in fluorescence intensities of ROS during Mn(II) exposure. Further, concentrations of superoxide and hydrogen peroxide from cells were detected respectively with and without Mn(II) exposure, exhibiting that when Mn(II) oxidation occurred, superoxide concentration significantly increased but hydrogen peroxide concentration significantly decreased. Particularly, superoxide produced by LLDRA6 was proven to be the oxidant for Mn(II) in the formation of Mn oxides. Finally, we predicted links between phenylacetic acid metabolism pathway and ROS during Mn(II) exposure, proposing that the excessive ROS, generated in response to Mn(II) exposure, transcriptionally activate phenylacetic acid catabolism presumably by increasing concentrations of highly reactive oxepins.


Metals ◽  
2021 ◽  
Vol 11 (10) ◽  
pp. 1636
Author(s):  
Sangyun Seo ◽  
Kyu Sung Han ◽  
Sung Il Lee ◽  
Myong Jun Kim

The processing of Cu, Co, and Zn at the Boleo project in Mexico involves two-stage (oxidation–reduction) leaching to extract a total of 85–88% Cu in 4 h. The first stage is an oxidation leaching using sulphuric acid (120 kg/tonne ore) at an Eh of 900 mV for 2 h. Then, the reduction stage takes place in 2 h with SO2 gas sparging for Mn and Co extraction at an Eh of 350–370 mV. The final extraction rates of metal values are 92% of Mn, 80% of Co, and 60% of Co, respectively, after 4 h of leaching at 70 °C. However, the same metal recoveries were obtained within 2 h using an equal amount of sulphuric acid and the addition of 25 kg of SO2 per tonne of ore in a single stage leaching in this research. In this case, the Fe extracted from the ore as Fe2+/Fe3+ is believed to have acted as an electrochemical couple contiguously leaching the Cu sulphide and Mn oxides, which also increased the Cu recovery as the Cu mineralised mostly intergrowths in these mineral structure matrices. A significant improvement was made in which the leaching time was halved to 2 h compared to 4 h in the previous plant design and current operation, involving the two-stage oxidation–reduction leaching.


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