Impact of Supersaturation Ratio on the Kinetics of Gas Evolution at Elevated Pressures

2020 ◽  
Vol 34 (12) ◽  
pp. 15812-15818
Author(s):  
Michael Angelo Miranda ◽  
Hariprasad J. Subramani ◽  
Clint P. Aichele
2020 ◽  
Vol 34 (5) ◽  
pp. 5537-5544
Author(s):  
Michael Angelo Miranda ◽  
Hariprasad J. Subramani ◽  
Sayeed A. Mohammad ◽  
Clint P. Aichele

Fuel ◽  
1986 ◽  
Vol 65 (10) ◽  
pp. 1364-1367 ◽  
Author(s):  
Chuang-tao Guo ◽  
Li-ming Zhang

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Chuanbo Li ◽  
Bo Wang ◽  
Xiang Li ◽  
Taihong Yan ◽  
Weifang Zheng

Abstract A new method is developed to calculate the dilution ratio N of the two reactant solutions during nucleation rate determination. When the initial apparent supersaturation ratio S N  = f(N) in the dilution tank is controlled between 1.66 and 1.67, the counted nuclei is the most, both nuclei dissolving and secondary nucleation avoided satisfactorily. Based on this methoed, Plutonium(IV) oxalate is precipitated by mixing equal volumes of tetravalent plutonium nitrate and oxalic acid solutions. Experiments are carried out by varying the supersaturation ratio from 8.37 to 22.47 and temperature from 25 to 50 °C. The experimental results show that the nucleation rate of plutonium(IV) oxalate in the supersaturation range cited above can be expressed by the equation R N  = A N exp(−E a /RT)exp[−B/(ln S)2], where A N  = 4.8 × 1023 m−3 s−1 , and E a  = 36.2 kJ mol−1, and B = 20.2. The crystal growth rate of plutonium(IV) oxalate is determined by adding seed crystals into a batch crystallizer. The crystal growth rate can be expressed by equation G(t) = k g exp(−E’ a /RT) (c − c eq) g , where k g  = 7.3 × 10−7 (mol/L)−1.1(m/s), E’ a  = 25.7 kJ mol−1, and g = 1.1.


Fuel ◽  
2017 ◽  
Vol 196 ◽  
pp. 210-216 ◽  
Author(s):  
Markus Steibel ◽  
Stefan Halama ◽  
Andreas Geißler ◽  
Hartmut Spliethoff

1978 ◽  
Vol 56 (7) ◽  
pp. 915-924 ◽  
Author(s):  
Brian E. Conway ◽  
J. C. Currie

For studies on effects of pressure on kinetics of electrode processes (Parts I, II), reversible reference electrodes suitable for use in a completely enclosed high-pressure bomb are required. The electrodes must exhibit reversible behaviour over the pressure range employed in the experiments, i.e., their changes of emf with increasing and decreasing changes of pressure must be reproducible and correspond to the respective volume changes in the reactions.A series of reversible reference electrodes is examined over a range of pressures up to ca. 2500 bars. The Pd–H/H+ and Ag, AgCl/Cl− reference electrodes are found to behave very satisfactorily at elevated pressures; the Pt,H2/H+ electrode is, however, less satisfactory, due to problems associated with dissolved H2.The results enable the volume of Pd–H and of H sorbed into Pd to be evaluated, together with estimates of the partial molar volume of H2 in aqueous HCl. These data enable the pressure-coefficients of metal–solution potential differences at individual reference electrodes to be evaluated. Such information is required for interpretation of effects of pressure on kinetics of electrode processes.


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