Adsorption of 60Co2+ on hydrous manganese oxide powder from aqueous solution

Verfasser / Beitragende:
[F. Granados Correa, J. Jiménez-Becerril]
Ort, Verlag, Jahr:
2004
Enthalten in:
Radiochimica Acta/International journal for chemical aspects of nuclear science and technology, 92/2/2004(2004-02-01), 105-110
Format:
Artikel (online)
ID: 378941267
LEADER caa a22 4500
001 378941267
003 CHVBK
005 20180305123652.0
007 cr unu---uuuuu
008 161128e20040201xx s 000 0 eng
024 7 0 |a 10.1524/ract.92.2.105.27459  |2 doi 
035 |a (NATIONALLICENCE)gruyter-10.1524/ract.92.2.105.27459 
245 0 0 |a Adsorption of 60Co2+ on hydrous manganese oxide powder from aqueous solution  |h [Elektronische Daten]  |c [F. Granados Correa, J. Jiménez-Becerril] 
520 3 |a Hydrous manganese oxide (HMO) was synthesized and its ability to sorb 60Co2+ from aqueous solution was studied under static conditions as a function of contact time, cobalt concentration (10-2-10-7M), temperature (303-333K) and pH of adsorptive solution (2.2-11.4). X-ray diffraction was used in characterization of synthesized HMO. Low concentration of 60Co2+ solution, high pH and high temperature were the most favorable conditions for the adsorption process. The results show that the removal process is complete in 40 minutes, obeys a first order rate law and can be described using the Freundlich adsorption model. The standard enthalpy of the system was ΔH0 = 12.5 ± 0.2 kJ mol-1 and cobalt desorption indicates that the uptake process proceeds via cation exchange. The removal of cobalt ions by HMO appears to be endothermic and irreversible. The values of calculated ΔG0 and ΔS0 were -17.0 ± 3.0 kJ mol-1 and (9.8 ± 0.2) × 10-2 kJ K-1 mol-1 respectively, this indicates spontaneity of the process and the degree of freedom of ions is increased by adsorption. 
540 |a © 2004 Oldenbourg Wissenschaftsverlag GmbH 
690 7 |a Laboratory techniques, experiments  |2 nationallicence 
690 7 |a Analytical chemistry  |2 nationallicence 
690 7 |a Inorganic chemistry  |2 nationallicence 
700 1 |a Granados Correa  |D F.  |4 aut 
700 1 |a Jiménez-Becerril  |D J.  |4 aut 
773 0 |t Radiochimica Acta/International journal for chemical aspects of nuclear science and technology  |d Oldenbourg Wissenschaftsverlag GmbH  |g 92/2/2004(2004-02-01), 105-110  |x 0033-8230  |q 92:2/2004<105  |1 2004  |2 92  |o ract 
856 4 0 |u https://doi.org/10.1524/ract.92.2.105.27459  |q text/html  |z Onlinezugriff via DOI 
908 |D 1  |a research article  |2 jats 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1524/ract.92.2.105.27459  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Granados Correa  |D F.  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Jiménez-Becerril  |D J.  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Radiochimica Acta/International journal for chemical aspects of nuclear science and technology  |d Oldenbourg Wissenschaftsverlag GmbH  |g 92/2/2004(2004-02-01), 105-110  |x 0033-8230  |q 92:2/2004<105  |1 2004  |2 92  |o ract 
900 7 |b CC0  |u http://creativecommons.org/publicdomain/zero/1.0  |2 nationallicence 
898 |a BK010053  |b XK010053  |c XK010000 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-gruyter