Add time:08/02/2019         Source:sciencedirect.com

Chromium catalysts were prepared by the saturating chemisorption of chromium(III) acetylacetonate (Cr(acac)3) at 200 °C on alumina and on alumina that had been surfaced with aluminum nitride. According to elemental analysis, infrared spectroscopy, and electron spin resonance spectroscopy, chemisorption occurred through ligand exchange reaction of Cr(acac)3 with surface OH and NHx groups and dissociation of Cr(acac)3 or Hacac on coordinatively unsaturated sites on the surface. Steric hindrance imposed by the acac ligands defined saturation of the surface with adsorbed species; the same chromium loading (0.64±0.06 atoms per nm2) was obtained on all supports. After removal of the ligands with oxygen, water, or ammonia, the samples were active in isobutane dehydrogenation. For chromium sites with high activity, nearby oxygen ions were needed. The activity of a Cr3+ ion was mainly determined by its environment and not by whether it had been formed through reduction.

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