2011
DOI: 10.2172/1011765
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Amineborane Based Chemical Hydrogen Storage - Final Report

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Cited by 12 publications
(25 citation statements)
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“…[1, [7][8][9][10] For example, the DOE recently decided to no longer pursue the use of NaBH 4 as a H 2 storage material, in part because of inefficient regeneration. We thus endeavored to find an energy-efficient regeneration process for the spent fuel from H 2 -depleted AB.…”
mentioning
confidence: 99%
See 1 more Smart Citation
“…[1, [7][8][9][10] For example, the DOE recently decided to no longer pursue the use of NaBH 4 as a H 2 storage material, in part because of inefficient regeneration. We thus endeavored to find an energy-efficient regeneration process for the spent fuel from H 2 -depleted AB.…”
mentioning
confidence: 99%
“…Representative structure of polyborazylene (PB). [8] To transform the products of Scheme 2 into AB, a reductant is required. Bu 3 SnH was judged to be a good starting point, as the reagent is commercially available and a literature report suggested a possible Bu 3 SnH regeneration method by decarboxylation of a tin formate.…”
mentioning
confidence: 99%
“…500°C, above which, evidence for boron nitride is seen [55] ) lead to products of the type (H 2 NBH 2 ) n and/or (HNBH) n . Similar strategies for regenerating AB from mixtures of these products have been proposed by Sneddon [56,57] and Mertens [58] that do not depend on the nature of (H 2 NBH 2 ) n or (HNBH) n by using an acid (HX) to form B-X bonds and then conversion of those B- Table 1. Calculated digestion enthalpies of borazine (gas-phase: B3LYP/DZVP2, cc-pVDZ-PP for tin).…”
Section: Polyborazylenementioning
confidence: 91%
“…Numerous examples of catalytically amended AB were demonstrated over the course of the CHSCoE. Homogenous catalysis efforts included Lewis acids [83], non-nucleophilic bases (i.e., Proton Sponge) [84], and various transition metals [83,[85][86][87][88]. One of the most effective homogenous catalysts was demonstrated by Baker et al [89] using nickel N-heterocyclic carbene (Ni-NHC) complex generated through an in situ reaction with bis(cyclooctadiene)Ni(0).…”
Section: Ammonia Boranementioning
confidence: 99%
“…Sneddon et al demonstrated the unique attributes of ILs for activating AB by reacting 1-butyl-3-methylimidazolium chloride (bmimCl) with AB (50:50 wt.%) at 358 K [31,91]. The AB-IL mixture exhibited no induction period and released 1.0 H 2 -equivalent in 67 min and 2.2 H 2 -equivalents total over 330 min which compares very favorably to thermolysis of AB at the same temperature releasing ~0.8 H 2 -equivalents after 360 min and an 180 min induction period.…”
Section: Ammonia Boranementioning
confidence: 99%