Abstract
A Rh-Zn compound was synthesized by exposing Rh to a fixed pressure of Zn vapor. After keeping Rh and Zn in a sealed container for 10 days at 1173 K and 1093 K (900 °C and 820 °C), respectively, an unreported compound was obtained. Its chemical composition was determined to be RhZn3, and X-ray diffraction analysis revealed it to have a face-centered tetragonal structure (a = b = 3.78 Å and c = 3.88 Å). The dissolution rate of Rh from the RhZn3 in hydrochloric acid was measured using a channel flow, double-electrode method, and it was found to be more than 100 times greater than that from pure Rh. The result verified the possibility of a Rh recovery process in which Rh is exposed to Zn vapor prior to acid leaching to enhance its dissolution.
Similar content being viewed by others
References
D. Jollie: Platinum 2009, Johnson Matthey Plc., Hertfordshire, U.K., 2009.
S. Matsumoto and H. Shinjoh: Adv. Chem. Eng., 2008, vol. 33, pp. 1–47.
J.S. Yoo: Catal. Today, 1998, vol. 44, pp. 27–46.
F. Habashi: Handbook of Extractive Metallurgy, Wiley-VCH, Weinheim, Germany, 1997.
Y. Kayanuma, T.H. Okabe, T. Mitsuda, and M. Maeda: J. Alloy. Compd., 2004, vol. 365, pp. 211–20.
Y. Kayanuma, T.H. Okabe, and M. Maeda: Metall. Mater. Trans. B, 2004, vol. 35B, pp. 817–24.
J. Itoh, Y. Kayanuma, M. Miyake, H. Kimura, and M. Maeda: Lead & Zinc ‘05, Proc. Int. Symp. on Lead and Zinc Processing, Kyoto, Japan, 2005, p. 1157.
H. Sasaki, M. Miyake, and M. Maeda: J. Electrochem. Soc., 2010, vol. 157, pp. E82–E87.
H. Sasaki, T. Nagai, and M. Maeda: J. Alloy Compd., 2010, vol. 504, pp. 475–78.
H. Sasaki and M. Maeda: J. Electrochem. Soc., 2010, vol. 157, pp. C414–18.
J. Llopis, I.M. Tordesillas, and M. Muňiz: Electrochim. Acta, 1965, vol. 10, pp. 1045–55.
D. Cozzi and F. Pantani: J. Inorg. Nucl. Chem., 1958, vol. 8, pp. 385–98.
Denkikagaku Binran (in Japanese), The Electrochemical Society of Japan, Maruzen, Tokyo, Japan, 2000.
J.A. Harrison and J. Thompson: J. Electroanal. Chem. Interfacial Electrochem., 1973, vol. 43, pp. 405–13.
L.A. Kibler, M. Kleinert, and D.M. Kolb: J. Electroanal. Chem., 1999, vol. 467, pp. 249–57.
T. Tsuru: Mater. Sci. Eng. A, 1991, vol. 146A, pp. 1–14.
N. Gross, G. Kotzyba, B. Kunnen, and W. Jeitschko: Z. Anorg. Allg. Chem., 2001, vol. 627, pp. 155–63.
L. Pauling: Proc. Natl. Acad. Sci. USA, 1989, vol. 86, pp. 1431–33.
Acknowledgments
H. Sasaki appreciates the Research Fellowship for Young Scientist (Grant DC2, No. 20-10341) from the Japan Society for the Promotion of Science (JSPS). This work was supported financially in part by a Grant-in-Aid for JSPS Fellows. It was also supported by the Ministry of the Environment in Japan through a Grant-in-Aid for Scientific Research about Establishing a Sound Material-Cycle Society (Grant K2120). The authors appreciate the assistance offered by Dr. T. Nagai and Mr. H. Kimura (The University of Tokyo).
Author information
Authors and Affiliations
Corresponding author
Additional information
Manuscript submitted November 18, 2010.
Rights and permissions
About this article
Cite this article
Sasaki, H., Maeda, M. Enhanced Dissolution of Rh from RhZn3 Formed Through Zn Vapor Pretreatment. Metall Mater Trans B 43, 443–448 (2012). https://doi.org/10.1007/s11663-012-9637-3
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11663-012-9637-3