Published September 2018 | Version v1
Journal article

α- and β-CoNi binary hydroxides nanostructures: Synthesis, characterization, and application as heterogeneous catalysts

  • 1. Department of Chemistry, Shahid Bahonar University of Kerman, 76169-133 Kerman (Iran, Islamic Republic of)
  • 2. Department of Basic Sciences, Sari Agricultural Sciences and Natural Resources University, Sari (Iran, Islamic Republic of)

Description

The aim of this study is to show that α- and β-CoNi binary hydroxides nanostructures can be used as heterogeneous catalysts in the oxidation of benzyl alcohol, N-formylation of aniline, and the Claisen–Schmidt condensation. The catalysts were synthesized by hydrothermal method and characterized by XRD, FE-SEM/EDX, FT-IR, TGA, UV–vis and N2 adsorption-desorption techniques. The α-phase is similar to layered double hydroxide (LDH), while β-phase is isostructural with brucite. In all of the three reactions, the conversion enhanced by increasing the amount of catalysts from 10 to 30 mg, and the catalytic activity of α-phase was better than β-phase. In benzyl alcohol oxidation, the best conversion for α- and β-phases was 90% and 80%, respectively, under solvent-free conditions. In N-formylation, the best yield for both catalysts was obtained 95% in solvent-free conditions. However, the time required for α-phase to reach this amount was a quarter of that for β-phase. For the Claisen–Schmidt condensation, the best yield was obtained at 90 °C, which was 70% and 50% for α- and β-CoNi binary hydroxides, respectively. Both catalysts were stable and subsequent to each step of recovery and reuse, no significant loss in activity was observed.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jssc.2018.06.018

Additional details

Identifiers

DOI
10.1016/j.jssc.2018.06.018;
PII
S0022459618302597;

Publishing Information

Journal Title
Journal of Solid State Chemistry (Print)
Journal Volume
265
Journal Page Range
p. 248-256
ISSN
0022-4596
CODEN
JSSCBI

Optional Information

Notes
© 2018 Elsevier Inc. All rights reserved.