Dissolution Kinetics of Cathode of Spent Lithium Ion Battery in Hydrochloric Acid Solutions

2013 ◽  
Vol 94 (1) ◽  
pp. 13-16 ◽  
Author(s):  
Mohammad Al Hossaini Shuva ◽  
A. S. W. Kurny
2016 ◽  
Vol 166 ◽  
pp. 205-213 ◽  
Author(s):  
Shilong Wei ◽  
Junshen Liu ◽  
Shengxiao Zhang ◽  
Xiaoliang Chen ◽  
Qingqing Liu ◽  
...  

1967 ◽  
Vol 45 (5) ◽  
pp. 515-519 ◽  
Author(s):  
E. Buncel ◽  
P. R. Bradley

The kinetics of the hydrolysis of methyl 2-chloro-2-deoxy-β-D-glucopyranoside have been determined in hydrochloric acid solutions over a range of acid concentrations and temperatures. Chloro substitution reduces the rate by a factor of 35 compared with the hydroxy analogue. Application of the Hammett criterion indicates a unimolecular (A-1) mechanism of hydrolysis, as does application of the Bunnett criterion. The entropy of activation, however, is considerably smaller than that observed for the hydrolysis of methyl β-d-glucopyranoside. This is interpreted as being indicative of partial A-2 character.


1972 ◽  
Vol 50 (11) ◽  
pp. 1698-1707 ◽  
Author(s):  
B. R. James ◽  
M. Kastner

In the presence of iron(III) or other oxidants, aqueous acid chloride solutions of RhCl5(H2O)2− catalyze under mild conditions the oxidation of ethylene to acetaldehyde. The kinetics of the reaction measured by gas-uptake techniques indicate the presence of both ethylene dependent and independent paths. Besides fully protonated anions, hydroxy species such as RhCl5 (OH)3− and RhCl4(OH)(H2O)2−, although present in very small concentrations, are significantly reactive towards ethylene. A mechanism, based on that postulated for a similar palladium(II) system in the well-known Wacker process, is presented. Under our reaction conditions the slow steps in the rhodium system involve formation of π-complexes in the ethylene dependent paths and the formation of tetrachlororhodate(III) complexes in the ethylene independent paths. Iron(III) regenerates the rhodium(III) catalyst by oxidation of the rhodium(I). Rate constants are estimated for the various reaction paths.


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