Volatilization Behavior of Li/Na Carbonate as an Electrolyte in MCFC

2019 ◽  
Vol 12 (1) ◽  
pp. 355-360 ◽  
Author(s):  
Kimihiko Sugiura ◽  
Masatsugu Soga ◽  
Makoto Yamauchi ◽  
Kazumi Tanimoto
2014 ◽  
Vol 127 ◽  
pp. 117-123 ◽  
Author(s):  
G. Hehar ◽  
O. Fasina ◽  
S. Adhikari ◽  
J. Fulton

Fuel ◽  
2004 ◽  
Vol 83 (1) ◽  
pp. 39-45 ◽  
Author(s):  
Hailiang Lu ◽  
Haokan Chen ◽  
Wen Li ◽  
Baoqing Li

2015 ◽  
Vol 144 ◽  
pp. 33-39 ◽  
Author(s):  
Yuanbo Zhang ◽  
Bingbing Liu ◽  
Zijian Su ◽  
Jun Chen ◽  
Guanghui Li ◽  
...  

MRS Advances ◽  
2020 ◽  
Vol 5 (5-6) ◽  
pp. 195-206
Author(s):  
Emily T. Nienhuis ◽  
John S. McCloy

ABSTRACTThis study seeks to understand the low temperature reactions of the salt phase that occur during the vitrification of Hanford Low Activity Waste (LAW). Salts (such as nitrates, sulfates, carbonates, halides, etc.) play a key role in these low temperature reactions as they sequentially melt, decompose, and volatilize during batch-to-glass conversion. To further understand these complex processes, simplified LAW melts containing oxyanion salts (sodium salts of carbonate, sulfate, and/or nitrate) and early melting glass formers (boric acid) have been evaluated using thermal analysis, infrared absorption spectroscopy, and X-ray diffraction. Results from this study indicate that the volatilization behavior of particular salts is influenced by the presence or absence of other salts. NaNO3 volatilization is decreased by the presence of Na2SO4. The addition of either Na2SO4 or NaNO3 to the system may enhance the volatilization of Na2CO3. In all cases, Na2SO4 was retained after melting and was often found to be in two different crystalline phases upon quenching.


Metals ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 1348
Author(s):  
Jianhua Chu ◽  
Yanping Bao

The volatilization loss of manganese during the vacuum smelting process is one of the key factors that determines the manufacturing cost and quality of manganese steel. In this study, the laboratory experiments and thermodynamic calculations were performed to investigate volatilization behavior of manganese from molten steels with different alloying methods in vacuum process. Based on the thermodynamic analysis, with the increase of manganese content, the partial vapor pressure of the manganese component increased, resulting in manganese being easily volatilized from molten steel. The carbon content in the steel shows an evident influence on partial vapor pressure of manganese component, and a higher carbon content in steel leads to a lower partial vapor pressure of manganese, but it not influenced by the silicon content. Compared with the alloying method of high carbon ferromanganese, the volatilization loss of manganese in the alloying method of silicon manganese presents faster decay, agreeing well with the thermodynamic analysis. Besides, the volatile fraction generated in the alloying method of high-carbon ferromanganese is composed of a large amount of MnO nanorods with a lateral length approximately 500 nm and a small number of Mn3O4/Mn nanoparticles with a diameter less than 500 nm. Additionally, the volatile fraction generated in the alloying method of silicon manganese shows Mn3O4 nanoparticles as the main phase. It can be inferred that the existence of the manganese oxide phase is attributed to the high chemical activity of nanoscale particles within air.


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