Related Experiment Video
Updated: Jun 1, 2026
Supercritical Nitrogen Processing for the Purification of Reactive Porous Materials
Published on: May 15, 2015
Promotion of hydrogen release from ammonia borane with magnesium nitride
Junhong Luo1, Xiangdong Kang, Zhanzhao Fang
1Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chinese Academy of Sciences, Shenyang, 110016, China.
Abstract:
Hydrogen release from ammonia borane (NH(3)BH(3), AB) can be greatly promoted by mechanical milling with magnesium nitride (Mg(3)N(2)). For example, a post-milled 6AB/Mg(3)N(2) sample started to release hydrogen from ∼65 °C and gave a material-based hydrogen capacity of ∼11 wt% upon heating to 300 °C. In addition to the improved dehydrogenation kinetics, the 6AB/Mg(3)N(2) sample also showed satisfactory performance in suppressing the volatile byproducts. X-ray diffraction, Fourier transform infrared spectroscopy and solid-state (11)B MAS NMR, as well as a series of designed experiments, were carried out to gain mechanistic understanding of the property improvements that arise from addition of Mg(3)N(2). Our study found that the formation of 3Mg(NH(2)BH(3))(2)·2NH(3), which is in single or mixed amidoborane ammoniate phases in nature, is an important mechanistic step in the dehydrogenation process of the 6AB/Mg(3)N(2) sample.
More Related Videos
08:40Synthesis of Metal Nanoparticles Supported on Carbon Nanotube with Doped Co and N Atoms and its Catalytic Applications in Hydrogen Production
Published on: December 6, 2021
06:32A Simple, Low-cost, and Robust System to Measure the Volume of Hydrogen Evolved by Chemical Reactions with Aqueous Solutions
Published on: August 17, 2016
Related Concept Videos
03:08Hydroboration-Oxidation of Alkenes
02:36Regioselectivity and Stereochemistry of Hydroboration
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn stereochemistry.
00:55Nitriles to Amines: LiAlH4 Reduction
As shown below, the mechanism involves three steps. Firstly, the hydride ion acting as a nucleophile attacks the nitrile carbon to form an anion. In the second step, a second equivalent of the hydride ion attacks the anion to...
02:47Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
02:15Preparation of Alcohols via Addition Reactions
The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...
01:17Radical Anti-Markovnikov Addition to Alkenes: Mechanism
The mechanism starts with chain initiation, which involves two steps. In the first chain initiation step, a weak peroxide bond is homolytically cleaved upon mild heating to form two alkoxy radicals. In the second initiation step, a hydrogen atom is abstracted by the alkoxy radical...