Molecular-level insights into mercury removal mechanism by pyrite

2018 ◽  
Vol 344 ◽  
pp. 104-112 ◽  
Author(s):  
Yingju Yang ◽  
Jing Liu ◽  
Feng Liu ◽  
Zhen Wang ◽  
Sen Miao
Fuel ◽  
2019 ◽  
Vol 235 ◽  
pp. 326-335 ◽  
Author(s):  
Dongyang Hong ◽  
Jinsong Zhou ◽  
Changxing Hu ◽  
Qixing Zhou ◽  
Juezhen Mao ◽  
...  

2021 ◽  
Vol 118 (5) ◽  
pp. 513
Author(s):  
Shan Zhu ◽  
Na Yang ◽  
Lin Zhang

In the present work, Scanning Electron Microscope (SEM) and Energy Dispersive X-ray Spectroscopy (EDS) were employed in the investigation of roasting mechanism, roasting dynamic model, control step of soda roasting process of selenium–mercury material. The results indicated that at the beginning of the roasting process, the control step might be interface chemical reaction for the first 30 min, and the kinetic equation might be 1−(1−R)⅓ = Kt with a activation energy E1 = 40.50 kT/mol. However, as the roasting proceeded, internal diffusion gradually became the control step for 90–135 min, and the kinetic equation might be 1−⅔R−(1−R)⅔ = Dt with a activation energy E2 = 6.75 kT/mol. The SEM analysis of the roasted selenium–mercury materials indicated that the dynamic model of soda roasting attributed to the shrinkage model was reasonable. Combined with the results obtained by SEM and EDS of the roasted selenium–mercury materials, we concluded that the addition of too much Na2CO3 might lead to the formation of molten crystalline phase in the inner of the roasted selenium–mercury materials, changing the mercury removal mechanism of the roasting process. Meanwhile, Se had a tendency to segregate at where the content of Na was relatively high. In order to study the mechanism of diffusion, Na2O2 of 9% was added to one of the samples. According to the results, we concluded that the diffusion of products (such as HgxOy) from the inside of the raw material was the control step of internal diffusion.


2018 ◽  
Vol 57 (23) ◽  
pp. 7889-7897 ◽  
Author(s):  
Fenghua Shen ◽  
Jing Liu ◽  
Dawei Wu ◽  
Chenkai Gu ◽  
Yuchen Dong

2022 ◽  
Vol 423 ◽  
pp. 127198
Author(s):  
Xinze Geng ◽  
Xiaoshuo Liu ◽  
Xunlei Ding ◽  
Qiang Zhou ◽  
Tianfang Huang ◽  
...  

2004 ◽  
Vol 69 (12) ◽  
pp. 1111-1120 ◽  
Author(s):  
Zoran Odanovic ◽  
M. Djurdjevic

An investigation of silver dental amalgam decomposition and the mercury removal mechanism was performed. The decomposition process was analyzed during thermal treatment in the temperature interval from 400 ?C to 850 ?C and for times from 0.5 to 7.5 h. The chemical compositions of the silver dental amalgam alloy and the treated alloy were tested and microstructure analysis using optical and scanning electron microscopy was carried out. The phases were identified using energy disperse electron probe microanalysis. A mechanism for the mercury removal process from silver dental amalgam alloy is suggested.


Author(s):  
F.J. Sjostrand

In the 1940's and 1950's electron microscopy conferences were attended with everybody interested in learning about the latest technical developments for one very obvious reason. There was the electron microscope with its outstanding performance but nobody could make very much use of it because we were lacking proper techniques to prepare biological specimens. The development of the thin sectioning technique with its perfectioning in 1952 changed the situation and systematic analysis of the structure of cells could now be pursued. Since then electron microscopists have in general become satisfied with the level of resolution at which cellular structures can be analyzed when applying this technique. There has been little interest in trying to push the limit of resolution closer to that determined by the resolving power of the electron microscope.


Author(s):  
E. Loren Buhle ◽  
Pamela Rew ◽  
Ueli Aebi

While DNA-dependent RNA polymerase represents one of the key enzymes involved in transcription and ultimately in gene expression in procaryotic and eucaryotic cells, little progress has been made towards elucidation of its 3-D structure at the molecular level over the past few years. This is mainly because to date no 3-D crystals suitable for X-ray diffraction analysis have been obtained with this rather large (MW ~500 kd) multi-subunit (α2ββ'ζ). As an alternative, we have been trying to form ordered arrays of RNA polymerase from E. coli suitable for structural analysis in the electron microscope combined with image processing. Here we report about helical polymers induced from holoenzyme (α2ββ'ζ) at low ionic strength with 5-7 mM MnCl2 (see Fig. 1a). The presence of the ζ-subunit (MW 86 kd) is required to form these polymers, since the core enzyme (α2ββ') does fail to assemble into such structures under these conditions.


Author(s):  
John H. Luft

With information processing devices such as radio telescopes, microscopes or hi-fi systems, the quality of the output often is limited by distortion or noise introduced at the input stage of the device. This analogy can be extended usefully to specimen preparation for the electron microscope; fixation, which initiates the processing sequence, is the single most important step and, unfortunately, is the least well understood. Although there is an abundance of fixation mixtures recommended in the light microscopy literature, osmium tetroxide and glutaraldehyde are favored for electron microscopy. These fixatives react vigorously with proteins at the molecular level. There is clear evidence for the cross-linking of proteins both by osmium tetroxide and glutaraldehyde and cross-linking may be a necessary if not sufficient condition to define fixatives as a class.


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