Synthesis of Copper(II)-Containing Nickel(II) Hydroxide Particles as Precursors of Copper(II)-Substituted Nickel(II) Oxides
Copperd(II)-containing nickel(II) hydroxide particles, i.e., α-Ni1-xCux(OH)2 (0 < x ≤ 0.4), have been prepared by aging 0.5 mol dm-3 urea, Ni(NO3)2, and Cu(NO3)2 solutions at 363 K. After 3 h, coprecipitation is almost complete. The formed solids, characterized by powder X-ray diffraction, sc...
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American Chemical Society
1998
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024 | 7 | |2 scopus |a 2-s2.0-0542372748 | |
040 | |a Scopus |b spa |c AR-BaUEN |d AR-BaUEN | ||
030 | |a CMATE | ||
100 | 1 | |a Jobbágy, M. | |
245 | 1 | 0 | |a Synthesis of Copper(II)-Containing Nickel(II) Hydroxide Particles as Precursors of Copper(II)-Substituted Nickel(II) Oxides |
260 | |b American Chemical Society |c 1998 | ||
270 | 1 | 0 | |m Regazzoni, A.E.; Unidad de Actividad Química, Comn. Nac. de Ener. Atómica, Avenida del Libertador 8250, (1429) Buenos Aires, Argentina |
506 | |2 openaire |e Política editorial | ||
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520 | 3 | |a Copperd(II)-containing nickel(II) hydroxide particles, i.e., α-Ni1-xCux(OH)2 (0 < x ≤ 0.4), have been prepared by aging 0.5 mol dm-3 urea, Ni(NO3)2, and Cu(NO3)2 solutions at 363 K. After 3 h, coprecipitation is almost complete. The formed solids, characterized by powder X-ray diffraction, scanning electron microscopy, energy dispersion X-ray spectroscopy, and Fourier transform infrared spectroscopy, preserve the typical characteristics of α-Ni(OH)2. Still, their chemical composition, i.e., the copper-to-nickel ratio, is nearly that of the initial solutions. The analysis of the processes that take place during the formation of α-Ni1-xCux(OH)2 indicates that, although Cu(II) and Ni(II) precipitation are separate events, the simultaneity of am-Cu(OH)2 (amorphous copper(II) hydroxide) redissolution and α-Ni(OH)2 growth provides the appropriate conditions for the intercalation of aqueous Cu(II) species within the interlayer space of the growing α-Ni(OH)2 particles. Upon mild thermal treatment, i.e., T ≥ 523 K, α-Ni1-xCux(OH)2 powders are readily converted in Ni1-xCuxO (bunsenite), provided x ≤ 0.33; when x is larger than 0.33, the thermodynamically expected segregation of tenorite is realized. The ease of Ni1-xCuxO (bunsenite) formation is rationalized in terms of the topotatic relationship between the layered structure of the precursors and the rock salt structure of the mixed oxide. |l eng | |
593 | |a INQUIMAE, Fac. de Ciencias Exactas y Naturales, Ciudad Universitaria, (1428) Buenos Aires, Argentina | ||
593 | |a Unidad de Actividad Química, Comn. Nac. de Ener. Atómica, Avenida del Libertador 8250, (1429) Buenos Aires, Argentina | ||
700 | 1 | |a Soler-Illia, G.J.D.A.A. | |
700 | 1 | |a Regazzoni, A.E. | |
700 | 1 | |a Blesa, M.A. | |
773 | 0 | |d American Chemical Society, 1998 |g v. 10 |h pp. 1632-1637 |k n. 6 |p Chem. Mater. |x 08974756 |w (AR-BaUEN)CENRE-5532 |t Chemistry of Materials | |
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