scholarly journals Extraction Kinetics of Ni(II) in the Ni<sup>2+</sup>- SO<sub>4</sub><sup style="margin-left:-7px;">2-</sup>-Ac<sup>-</sup>(Na<sup>+</sup>, H<sup>+</sup>)-Cyanex 272 (H<sub>2</sub>A<sub>2</sub>)-Kerosene-3% (v/v) Octan-1-ol System Using Single Drop Technique

2013 ◽  
Vol 02 (02) ◽  
pp. 80-88 ◽  
Author(s):  
Ranjit Kumar Biswas ◽  
Aneek Krishna Karmakar ◽  
Muhammad Saidur Rahman
2002 ◽  
Vol 67 (1-3) ◽  
pp. 45-52 ◽  
Author(s):  
Muhammad Idiris Saleh ◽  
Md Fazlul Bari ◽  
Md Sariff Jab ◽  
Bahruddin Saad

2017 ◽  
Vol 9 (2) ◽  
pp. 255-266 ◽  
Author(s):  
R. K. Biswas ◽  
A. K. Karmakar ◽  
M. Mottakin

The titled system has been investigated using a single drop technique and flux (F) method of data treatment. In calculating fluxes, the time for drop formation and coalescence (?t = 0.75 s) is considered. At lower concentration region of vanadium, V(V), the rate of V(V) transfer is directly proportional to its concentration. With the increase in [V(V)], slowly extractable V(V) species are formed gradually resulting in decrease in rate. Rate is directly proportional to the square root of [TOA]. It is reported that the most favorable extractable V(V) species exists in maximum amount at pH 2, and so, log F vs pH plots show a maximum at pH~2. The flux of V(V) transfer in most cases is found to be decreased with increasing [NO3-]. Reaction orders with respect to [V(V)], pH and [NO3-] have been attempted to be estimated, but in vein due to non-linearity of plots in most cases. Activation energies for the present system is ~ -12 kJ/mol. This is unexpected but explained. Due to irregular variation of the composition of extractable species with [V(V)], [H+]; as well as temperature; it is not possible to elucidate the value of rate constant (k) and mechanism in simple way.


2016 ◽  
Vol 160 ◽  
pp. 1-5 ◽  
Author(s):  
Hui-fang Li ◽  
Li-juan Li ◽  
Dong Shi ◽  
Jin-feng Li ◽  
Lian-min Ji ◽  
...  

2007 ◽  
Vol 30 (9) ◽  
pp. 1165-1165
Author(s):  
R. K. Biswas ◽  
M. R. Ali ◽  
A. K. Karmakar ◽  
M. Kamruzzaman

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