Electrode potentials and thermodynamic data for aqueous ions. Copper, zinc, cadmium, iron, cobalt, and nickel

1968 ◽  
Vol 72 (8) ◽  
pp. 2902-2907 ◽  
Author(s):  
J. W. Larson ◽  
P. Cerutti ◽  
H. K. Garber ◽  
L. G. Hepler
Author(s):  
David M. Dawson ◽  
Dennis A. Walker ◽  
Mark Thornton-Pett ◽  
Manfred Bochmann

2021 ◽  
Author(s):  
Wenjing Yang ◽  
Yanhong Dong ◽  
Hongjian Sun ◽  
Xiaoyan Li

The synthesis and characterization of Fe, Co and Ni complexes supported by silylene ligands in recent ten years are summarized. Due to the decrease of electron cloud density on Si...


1969 ◽  
Vol 41 (3) ◽  
pp. 518-522 ◽  
Author(s):  
Jaroslav. Matousek ◽  
Vaclav. Sychra

2007 ◽  
Vol 20-21 ◽  
pp. 248-257 ◽  
Author(s):  
Stoyan N. Groudev ◽  
Plamen S. Georgiev ◽  
Irena Spasova ◽  
Marina Nicolova

Acid drainage waters generated in the uranium deposit Curilo, Bulgaria, were treated by means of different passive systems such as natural and constructed wetlands, alkalizing limestone drains, permeable reactive multibarriers and a rock filter, used separately or in different combinations. The waters had a pH in the range of about 2 – 4 and contained radionuclides (uranium, radium), heavy metals (copper, zinc, cadmium, lead, nickel, cobalt, iron, manganese), arsenic and sulphates in concentrations usually much higher than the relevant permissible levels for waters intended for use in agriculture and/or industry. The water flow rate through the individual systems was different and not stable, and varied in the range approximately from 0.02 to 1.5 l/s. Efficient removal of pollutants was achieved by means of these systems during the different climatic seasons, even during the cold winter months at water and ambient temperatures close to 0 oC. The removal was due to different mechanisms but microbial sulphate reduction, biosorption by living and dead plant biomass and chemical neutralization played the main roles.


1959 ◽  
Vol 37 (10) ◽  
pp. 1629-1636 ◽  
Author(s):  
J. R. MacEwan ◽  
J. U. MacEwan ◽  
L. Yaffe

The self-diffusion of nickel and the diffusion of Ni63 into iron, cobalt, and two iron–nickel alloys was studied using the technique of decrease in surface activity, The nickel self-diffusion results are compared to previously reported values. Nickel is found to diffuse more slowly than iron in the iron-rich portion of the iron–nickel system. The rate of nickel diffusion increases with increasing nickel content. A comparison is made between the present results for diffusion of Ni63 into iron, cobalt, and nickel with reported values for diffusion of Co60 and Fe59 in the same metals. In each solvent, the magnitudes of the activation energies, Q, are such that QNi > QCo > QFe.


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