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Wax: A benign hydrogen-storage material that rapidly releases H₂-rich gases through microwave-assisted catalytic decomposition.

ABSTRACT: Hydrogen is often described as the fuel of the future, especially for application in hydrogen powered fuel-cell vehicles (HFCV's). However, its widespread implementation in this role has been thwarted by the lack of a lightweight, safe, on-board hydrogen storage material. Here we show that benign, readily-available hydrocarbon wax is capable of rapidly releasing large amounts of hydrogen through microwave-assisted catalytic decomposition. This discovery offers a new material and system for safe and efficient hydrogen storage and could facilitate its application in a HFCV. Importantly, hydrogen storage materials made of wax can be manufactured through completely sustainable processes utilizing biomass or other renewable feedstocks.

SUBMITTER: Gonzalez-Cortes S

PROVIDER: S-EPMC5069496 | biostudies-literature | 2016 Oct

REPOSITORIES: biostudies-literature

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Wax: A benign hydrogen-storage material that rapidly releases H<sub>2</sub>-rich gases through microwave-assisted catalytic decomposition.

Gonzalez-Cortes S S Slocombe D R DR Xiao T T Aldawsari A A Yao B B Kuznetsov V L VL Liberti E E Kirkland A I AI Alkinani M S MS Al-Megren H A HA Thomas J M JM Edwards P P PP

Scientific reports 20161019

Hydrogen is often described as the fuel of the future, especially for application in hydrogen powered fuel-cell vehicles (HFCV's). However, its widespread implementation in this role has been thwarted by the lack of a lightweight, safe, on-board hydrogen storage material. Here we show that benign, readily-available hydrocarbon wax is capable of rapidly releasing large amounts of hydrogen through microwave-assisted catalytic decomposition. This discovery offers a new material and system for safe ...[more]

PMID: 27759014

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Project description:Seasonal heat storage is considered as one of the key elements on the path to a low-emission economy. Embedded in local district heating networks, they raise the share of renewable energies and balance out highly fluctuating supplies of e.g. solar systems or windmills. The technology of seasonal heat storage can be described as almost technically mature, with well-established concepts and some systems being in operation for a considerable time. Nevertheless, the operating experience gained to date also revealed two critical problems. On the one hand, even smallest leakages in sealing foils led to irreparable breakdowns. On the other hand, heat loss in the marginal areas was revealed as a key deficiency, preventing the technology from advancing towards global marketability. This study presents an experimental approach to address these two key issues in the field of seasonal energy storage. Two small-scale laboratory tests were carried out to test paraffin wax as a completely novel component in the marginal area of seasonal storages. This is based on two material properties: As hydrophobic and mobile medium, the warmed and molten paraffin should actively seal the fissures and holes in the event of leakage. Additionally, the latent heat storage properties of the paraffin wax should increase the systems' total storage capacity and reduce lateral heat losses via its low thermal conductivity. With retardation periods from 2.5 to 4 hours, the results show an effective phase change effect of the paraffin wax, which reduces energy losses and allows to buffer short-term, intensive loading and unloading processes. By storing up to 138 kJ/kg energy in the paraffin wax, increased capacities of application-scale pit storages by up to 40.70 MWh are to be expected. Additionally, the self-healing features could be successfully demonstrated: With only small losses of between 1.5 and 17%, the paraffin wax effectively sealed artificially incised leaks. Thereby, the mechanism was most effective for local defects. Following these positive demonstrations of feasibility, technical design questions still remain, which concern prevention of deformation of the paraffin wax. Once solved, this new component can then provide a path for further optimization of seasonal heat storage technologies.

Project description:The impact of ambient gas molecules (X), NO2, CO2 and SO2 on the structure, stability and decontamination activity of Cs8Nb6O19 polyoxometalate was studied computationally and experimentally. It was found that Cs8Nb6O19 absorbs these molecules more strongly than it adsorbs water and Sarin (GB) and that these interactions hinder nerve agent decontamination. The impacts of diamagnetic CO2 and SO2 molecules on polyoxoniobate Cs8Nb6O19 were fundamentally different from that of NO2 radical. At ambient temperatures, weak coordination of the first NO2 radical to Cs8Nb6O19 conferred partial radical character on the polyoxoniobate and promoted stronger coordination of the second NO2 adsorbent to form a stable diamagnetic Cs8Nb6O19/(NO2)2 species. Moreover, at low temperatures, NO2 radicals formed stable dinitrogen tetraoxide (N2O4) that weakly interacted with Cs8Nb6O19. It was found that both in the absence and presence of ambient gas molecules, GB decontamination by the Cs8Nb6O19 species proceeds via general base hydrolysis involving: (a) the adsorption of water and the nerve agent on Cs8Nb6O19/(X), (b) concerted hydrolysis of a water molecule on a basic oxygen atom of the polyoxoniobate and nucleophilic addition of the nascent OH group to the phosphorus center of Sarin, and (c) rapid reorganization of the formed pentacoordinated-phosphorus intermediate, followed by dissociation of either HF or isopropanol and formation of POM-bound isopropyl methyl phosphonic acid (i-MPA) or methyl phosphonofluoridic acid (MPFA), respectively. The presence of the ambient gas molecules increases the energy of the intermediate stationary points relative to the asymptote of the reactants and slightly increases the hydrolysis barrier. These changes closely correlate with the Cs8Nb6O19-X complexation energy. The most energetically stable intermediates of the GB hydrolysis and decontamination reaction were found to be Cs8Nb6O19/X-MPFA-(i-POH) and Cs8Nb6O19/X-(i-MPA)-HF both in the absence and presence of ambient gas molecules. The high stability of these intermediates is due to, in part, the strong hydrogen bonding between the adsorbates and the protonated [Cs8Nb6O19/X/H]+-core. Desorption of HF or/and (i-POH) and regeneration of the catalyst required deprotonation of the [Cs8Nb6O19/X/H]+-core and protonation of the phosphonic acids i-MPA and MPFA. This catalyst regeneration is shown to be a highly endothermic process, which is the rate-limiting step of the GB hydrolysis and decontamination reaction both in the absence and presence of ambient gas molecules.

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Wax: A benign hydrogen-storage material that rapidly releases H₂-rich gases through microwave-assisted catalytic decomposition.

Publications

Wax: A benign hydrogen-storage material that rapidly releases H<sub>2</sub>-rich gases through microwave-assisted catalytic decomposition.

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Wax: A benign hydrogen-storage material that rapidly releases H2-rich gases through microwave-assisted catalytic decomposition.

Publications

Wax: A benign hydrogen-storage material that rapidly releases H<sub>2</sub>-rich gases through microwave-assisted catalytic decomposition.

Similar Datasets

OmicsDI is part of the ELIXIR infrastructure

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Wax: A benign hydrogen-storage material that rapidly releases H₂-rich gases through microwave-assisted catalytic decomposition.