Study of Support Effects on the Reduction of Ni2+ Ions in Aqueous Hydrazine

• Published in: Langmuir 2004-01, Vol.20 (1), p.208-213
• Main Authors: Boudjahem, Abdel-Ghani, Monteverdi, Serge, Mercy, Michel, Bettahar, Mohammed M
• Format: Article
• Language: English
• Subjects: Catalysis; Hydrazines - chemistry; Nickel - chemistry; Oxidation-Reduction; Particle Size; Silicon Dioxide - chemistry; Surface Properties; Temperature; Water - chemistry
• ISSN: 0743-7463; 1520-5827
• DOI: 10.1021/la035120+

We have studied the effect of silica of quartz-type on the reducibility of nickel acetate in aqueous hydrazine (80 °C, pH = 10−12) and metal particle formation. The obtained materials were characterized by X-ray diffraction, transmission electron microscopy, and thermodesorption experiments. With nickel acetate alone, the reduction was partial (45%) and a metal film at the liquid−gas interface or a powdered metal precipitate with an average particle size of 120 nm was obtained. In the presence of silica as the surfactant, the reduction of nickel acetate was total and the nickel phase deposited as a film on the support with an average particle size of 25 nm. Supported nickel acetate was also totally reduced. Crystallites of a mean particle size of about 3 nm were obtained. Decreasing the nickel content or increasing the hydrazine/nickel ratio decreased the metal particle size. Whiskers were formed for low nickel loadings. Hydrogen thermal treatment of the reduced phase showed that the organic acetate fragment, belonging to the precursor salt, still remained strongly attached to the nickel phase. The amount of the retained organic matrix depended on the metal particle size. Surface defects are suggested as active sites, which enhanced nickel ion reduction in the presence of silica as the surfactant or support. Metal−support interactions and the nucleation/growth rate were the main factors determining the size and morphology of the supported metal particles formed. The organic matrix covered the reduced nickel phase.