Revisiting the hydrogen storage behavior of the Na-O-H system

Solid-state reactions between sodium hydride and sodium hydroxide are unusual among hydride-hydroxide systems since hydrogen can be stored reversibly. In order to understand the relationship between hydrogen uptake/release properties and phase/structure evolution, the dehydrogenation and hydrogenation behavior of the Na-O-H system has been investigated in detail both ex- and in-situ. Simultaneous thermogravimetric-differential thermal analysis coupled to mass spectrometry (TG-DTA-MS) experiments of NaH-NaOH composites reveal two principal features: Firstly, an H2 desorption event occurring between 240 and 380 °C and secondly an additional endothermic process at around 170 °C with no associated weight change. In-situ high-resolution synchrotron powder X-ray diffraction showed that NaOH appears to form a solid solution with NaH yielding a new cubic complex hydride phase below 200 °C. The Na-H-OH phase persists up to the maximum temperature of the in-situ diffraction experiment shortly before dehydrogenation occurs. The present work suggests that not only is the inter-phase synergic interaction of protic hydrogen (in NaOH) and hydridic hydrogen (in NaH) important in the dehydrogenation mechanism, but that also an intra-phase Hδ+… Hδ– interaction may be a crucial step in the desorption process

Facile preparation of β-/γ-MgH2 nanocomposites under mild conditions and pathways to rapid dehydrogenation

A magnesium hydride composite with enhanced hydrogen desorption kinetics can be synthesized via a simple wet chemical route by ball milling MgH2 with LiCl as an additive at room temperature followed by tetrahydrofuran (THF) treatment under an Ar atmosphere. The as-synthesized composite comprises ca. 18 mass% orthorhombic γ-MgH2 and 80 mass% tetragonal β-MgH2 as submicron-sized particles. The β-/γ-MgH2 nanocomposite exhibits a dehydrogenation capacity of 6.6 wt.% and starts to release hydrogen at ~260 °C; ca. 140 °C lower than that of commercial MgH2. The apparent activation energy for dehydrogenation is 115±3 kJ mol-1, which is ca. 46 % lower than that of commercial MgH2. Analysis suggests that the meta-stable γ-MgH2 component either directly dehydrogenates exothermically or first transforms into stable β-MgH2 very close to the dehydrogenation onset. The improved hydrogen release performance can be attributed both to the existence of the MgH2 nanostructure and to the presence of γ-MgH2

Unusual structural phenomena in the reaction of copper and nickel dihalides with NH_3(g) at ambient conditions

No abstract available

Recent progress in the synthesis of nanostructured magnesium hydroxide

This review highlights synthetic routes for producing nanostructured magnesium hydroxide and focuses on how these various preparative approaches can produce Mg(OH)2 nanoparticles with controlled size and morphology. Mg(OH)2 nanocrystals with rod-, needle-, hollow tube- or platelet-like morphology can be synthesised by the modification of chemical and physical experimental parameters such as the selection of magnesium precursor, solvent and temperature or by employing surface modifiers and templates. Techniques based on hydrothermal/solvothermal treatments, microwave heating and (co-)precipitation are dominant in the production of Mg(OH)2 at the nanoscale, but other materials design approaches are now emerging. Bulk Mg(OH)2 has been extensively studied over decades and finds use in a wide range of applications. Moreover, the hydroxide can also serve as a precursor for other commercially important materials such as MgO. Nanostructuring the material has proven extremely useful in modifying some of its most important properties – not least enhancing the performance of Mg(OH)2 as a non-toxic flame retardant – but equally it is creating new avenues of applied research. We evaluate herein the latest efforts to design novel synthesis routes to nano-Mg(OH)2, to understand the mechanisms of crystallite growth and to tailor microstructure towards specific properties and applications

Ammonia borane-based nanocomposites as solid state hydrogen stores for portable power applications

Ammonia borane (AB) based nanocomposites have been investigated with the aim of developing a promising solid-state hydrogen store that complies with the requirements of a modular polymer electrolyte membrane fuel cell (PEM FC) in a portable power pack system. AB-carbon nanocomposites (prepared via ball milling or solution-impregnation) demonstrate improved hydrogen release performance compared to AB itself in terms of onset temperature and hydrogen purity, while maintaining a gravimetric density of more than 5 wt. % H2. The most promising of these materials is an AB-AC (activated carbon) composite, synthesised via solution-impregnation with an optimal dehydrogenation temperature of 96 °C. When combined with an external nickel chloride filter downstream, no evolved gaseous by-products can be detected above 100 ppb. The feasibility of an AB-AC storage tank has been further endorsed by simulations in which the reaction rate and the hydrogen flux was found to be almost constant as the temperature front propagated from the bottom to the top of the tank after initiation

Reaching the continuum limit in lattice gauge theory - without a computer

The scaling slope of the anti-symmetric mass gap M of compact U(1)_{2+1} lattice gauge theory is obtained analytically in the Hamiltonian formalism using the plaquette expansion. Based on the first four moments of the Hamiltonian with respect to a one-plaquette mean field state the results demonstrate clear scaling of M at and beyond the transition from strong to weak coupling. The scaling parameters determined agree well with the range of numerical determinations available.Comment: 4 pages, 2 figure

Central Asia and the globalisation of the contemporary legal consciousness

What is the logic which governs the processes of legal globalization? How does the transnational proliferation of legal forms operate in the contemporary geo-juridical space? What are the main defining characteristics of the currently dominant mode of transnational legal consciousness and how can the concept of legal consciousness help us understand better the historical ebb and flow of the Western-led projects of good governance promotion in regions like Central Asia after the fall of the Soviet Union? Using Duncan Kennedy’s seminal essay Three Globalizations of Law and Legal Thought as its starting platform, this essay seeks to explore these and a series of other related questions, while also drawing on the work of the Greek Marxist lawyer-philosopher Nicos Poulantzas to help elucidate some latent analytical stress-points in Kennedy’s broader theoretical framework. Reacting against the neo-Orientalist tone adopted across much of the contemporary field of Central Asian studies, it develops an alternative account of the internal history of the legal-globalizational encounter between the Western-based reform entrepreneurs and the national legal-political elites in Central Asia in the post-1991 period, complementing it with a detailed description of the general institutional and discursive structures within which this encounter took place

Gasser-Leutwyler coefficients: A progress report

Last year, we reported our first results on the determination of Gasser-Leutwyler coefficients using partially quenched lattice QCD with three flavors of dynamical staggered quarks. We give an update on our progress in determining two of these coefficients, including an exhaustive effort to estimate all sources of systematic error. At this conference, we have heard about algorithmic techniques to reduce staggered flavor symmetry breaking and a method to incorporate staggered flavor breaking into the partially quenched chiral Lagrangian. We comment on our plans to integrate these developments into our ongoing program.Comment: 3 pages, 2 figures, Lattice2002(spectrum

What makes continuing education effective : perspectives of community pharmacists

Objective To explore how different aspects of the professional environment for Australian community pharmacists are perceived to be influencing the effectiveness of continuing education models in improving practice.Setting Australian community pharmacy.Methods A convenience sample of practising community pharmacists (n = 15) was recruited using the \u27snowballing\u27 technique to participate in one of four focus group teleconferences. Each focus group examined continuing education experiences from different professional perspectives and training needs (recent graduates, experienced practitioners, specialist practitioners and rural/remote practitioners).Key findings Facilitation of professional development by accreditation bodies, and new challenges resulting from the introduction of cognitive services were seen to promote a favourable environment for continuing education engagement. Complex continuing education delivery models combined with high costs and excessive workloads made it more difficult to engage with continuing education systems or try to apply knowledge to the workplace.Conclusion Results support findings from previous research that practice development requires a multifaceted approach with continuing education as just one component. Affordable and integrated models of continuing education are required in order to optimise efficacy for participants.<br /

Rapid surfactant-free synthesis of Mg(OH)2 nanoplates and pseudomorphic dehydration to MgO

Magnesium hydroxide nanoplates ca. 50 nm in thickness can be prepared over minute timescales via hydrothermal synthesis in a multimode cavity (MMC) microwave reactor. This approach allows ca. 1 g of single-phase Mg(OH)2 to be synthesised in under 3 minutes without the requirement of surfactants or non-aqueous solvents. The hydroxide nanomaterial dehydrates at temperatures &gt;200 K below that of the equivalent bulk material and can be utilised as a precursor for the pseudomorphic synthesis of nanoplates of MgO as investigated by TG-DTA-MS, XRD and SEM measurements. Equally, the pseudomorphic synthesis can be performed by irradiating the Mg(OH)2 nanomaterial with microwaves for 6 minutes to produce single phase MgO