The structure of vanadia species supported on zirconia depends on VOx surface density and on the temperature of catalyst oxidation pretreatments. X-ray diffraction and Raman and UV-visible spectroscopies show that supported VOx species form polyvanadate domains of increasing size and ultimately monolayers and clusters as vanadium surface density increases. Initial propene selectivities in oxida...

Ethanol (EtOH) decomposition has been widely studied in recent years. However, the initial dehydrogenation selectivity on catalytic surfaces, which plays a crucial role in EtOH partial oxidation and steam reforming, is not well understood. Here, density functional theory (DFT) was used to calculate the initial dehydrogenation selectivities of EtOH on monometallic and X/Au (X = Pd and Rh) close-...

Possessing high H(2) capacities and interesting dehydrogenation behavior, metal amidoborane ammoniates were prepared by reacting Ca(NH(2) )(2) , MgNH, and LiNH(2) with ammonia borane to form Ca(NH(2) BH(3) )(2) ⋅2 NH(3) , Mg(NH(2) BH(3) )(2) ⋅NH(3) , and Li(NH(2) BH(3) )(2) ⋅NH(3) (LiAB⋅NH(3) ). Insight into the mechanisms of amidoborane ammoniate formation and dehydrogenation was obtained b...

Tandem dehydrogenation-olefin-metathesis catalyst systems, comprising a pincer-ligated iridium-based alkane dehydrogenation catalyst and a molybdenum-based olefin-metathesis catalyst, are reported to effect the metathesis-cyclooligomerization of cyclooctane and cyclodecane to give cycloalkanes with various carbon numbers, predominantly multiples of the substrate carbon number, and polymers.

In previous studies, complex hydrides LiBH4 and Mg2FeH6 have been reported to undergo simultaneous dehydrogenation when ball-milled as composite materials (1 − x)LiBH4 + xMg2FeH6. The simultaneous hydrogen release led to a decrease of the dehydrogenation temperature by as much as 150 K when compared to that of LiBH4. It also led to the modified dehydrogenation properties of Mg2FeH6. The simulta...

Compared to C60, carbon nanotubes, and graphite, graphene more effectively lowers the dehydrogenation temperature and improves the dehydrogenation kinetics of LiAlH4. With 15 wt% graphene incorporation, the initial hydrogen release temperature is ~80 °C (60 °C lower than that of pristine LiAlH4).

Significant advantages result from combining the disparate hydrogen release pathways for ammonia-borane (AB) dehydrogenation using ionic liquids (ILs) and transition metal catalysts. With the RuCl(2)(PMe(3))(4) catalyst precursor, AB dehydrogenation selectivity and extent are maximized in an IL with a moderately coordinating ethylsulfate anion.

Herein we show that a previously unappreciated combination of CrAuPd alloy nanoparticles and amine-grafted silica support facilitates the liberation of CO-free H2 from dehydrogenation of formic acid with record activity in the absence of any additives at room temperature. Furthermore, their excellent catalytic stability makes them isolable and reusable heterogeneous catalysts in the formic acid...

The dehydrogenation properties of LiAlH4 doped with different Ti precursors (Ti, TiO2, and TiCl3) via ball milling are investigated. The results not only show significant decreases in the decomposition temperatures (Tdec) and activation energies (EA) of the first two dehydrogenation reaction steps of LiAlH4 by doping with TiO2 or TiCl3, but also reveal how each Ti precursor affects the dehydrog...