Destabilisation of magnesium hydride by germanium as a new potential multicomponent hydrogen storage system

MgH(2) has too high an operating temperature for many hydrogen storage applications. However, MgH(2) ball-milled with Ge leads to a thermodynamic destabilisation of >50 kJ mol(-1)(H(2)). This has dramatically reduced the temperature of dehydrogenation to 130 °C, opening up the potential for Mg-based multicomponent systems as hydrogen stores for a range of applications.     

A new Li-Al-N-H system for reversible hydrogen storage

Complex metal hydrides are considered as a class of candidate materials for hydrogen storage. Lithium-based complex hydrides including lithium alanates (LiAlH(4) and Li(3)AlH(6)) are among the most promising materials owing to its high hydrogen content. In the present work, we investigated dehydrogenation/rehydrogenation reactions of a combined system of Li(3)AlH(6) and LiNH(2). Thermogravimetric analysis (TGA) of Li(3)AlH(6)/3LiNH(2)/4 wt % TiCl(3)-(1)/(3)AlCl(3) mixtures indicated that a large amount of hydrogen (approximately 7.1 wt %) can be released between 150 degrees C and 300 degrees C under a heating rate of 5 degrees C/min in two dehydrogenation reaction steps. The results also show that the dehydrogenation reaction of the new material system is nearly 100% reversible under 2000 psi pressure hydrogen at 300 degrees C. Further, a short-cycle experiment has demonstrated that the new combined material system of alanates and amides can maintain its hydrogen storage capacity upon cycling of the dehydrogenation/rehydrogenation reactions.     

Preparation and hydrogen storage properties of an Li-Mg-N-H system

An Li-Mg-N-H system has been synthesized from Mg(NH₂)₂ and LiH in the ratio 3:8 by a ball-milling process and its dehydrogenation/rehydrogenation properties at around 190°C were investigated. XRD, FTIR and TG results showed that the system was composed of an LiH phase and an amorphous Mg(NH₂)₂ phase with a purity of 90%. A reversible hydrogen storage capacity of 4.7% was observed during the first cycle and more than 90% of the stored hydrogen was desorbed within 100 min for each cycle. However, only 4.2% and 2.9%, respectively, of hydrogen was observed during two subsequent dehydrogenation cycles. In situ GC results showed that no NH3 could be observed during the dehydrogenation process. On the basis of the SEM and XRD results, the loss in hydrogen storage capacity can be mainly attributed to agglomeration, oxidation and crystallization of the materials.     

Hydrogen desorption mechanism in a Li-N-H system by means of the isotopic exchange technique

The hydrogen desorption mechanism in the reaction from LiH + LiNH2 to Li2NH + H2 was examined by thermal desorption mass spectrometry, thermogravimetric analysis, and Fourier transform IR analyses for the products replaced by LiD or LiND2 for LiH or LiNH2, respectively. The results obtained indicate that the hydrogen desorption reaction proceeds through the following two-step elementary reactions mediated by ammonia: 2LiNH2 --> Li2NH + NH3 and LiH + NH3 --> LiNH2 + H2, where hydrogen molecules are randomly formed from four equivalent hydrogen atoms in a hypothetical LiNH4 produced by the reaction between LiH and NH3 according to the laws of probability.     

Synthesis and hydrogen storage behavior of Mg-Co-H system at nanometer scale

There are few reports on the hydrogen storage behavior study of Mg-Co-H system in the literature, although Mg₂CoH₅ has a much higher hydrogen capacity than Mg₂NiH₄. This is due to the great difficulty in the synthesis of Mg₂CoH₅ and Mg₂Co in convenient conditions. Here we successfully synthesized the nanostructured Mg₂CoH₅ and Mg₂Co from Mg and Co nanoparticles prepared by hydrogen plasma-metal reaction method. The reaction mechanism of the synthesis of the Mg-Co-H system was studied. The morphology of the Mg-Co-H system in nanometer scale was observed. The hydrogen absorption curves and the pressure-composition isotherm (P-C-T) properties of the Mg-Co-H system were studied. The van’t Hoff equations and the formation enthalpies and entropies of the produced Mg₂CoH₅ and Mg₃CoH₅ were obtained. The results were discussed by comparing with the corresponding ones of Mg-Co-H system by other groups and the ones of nanostructured Mg-H and Mg-Ni-H systems by our group.     

Effect of modified fly ash with hydrogen bromide on the adsorption efficiency of elemental mercury

Mercury is one of the most hazardous trace elements produced by coal-fired power plants. Mercury in the flue gas is predominately present as three different species: particulate mercury (Hg^p), oxidized mercury (Hg²⁺), and elemental mercury (Hg⁰). Of these three, elemental mercury is the most difficult to remove from flue gas streams due to its low reactivity and low solubility in water. With increasing production costs associated with activated carbon materials, and increasing restrictions on mercury emissions, the development of an alternative low cost absorbent to capture elemental mercury by using fly ash modified with bromide compounds is highly desirable. Modified fly ash is usually injected into the flue gas stream after the air pre-heater system of a coal-fired power plant to oxidize and subsequently absorb elemental mercury. Research on the quantity and method of modifying the bromide amended fly ash is needed to obtain the most efficient mercury capture rate. This study utilized the impregnation method to prepare three different fly ashes with hydrogen bromide (HBr). Adsorption capabilities of the modified fly ashes were then examined using a fixed bed reactor. Thermogravimetric (TG) analysis was employed to quantify the amount of hydrogen bromide in the modified fly ash, which was subsequently compared to the water extraction method using ion chromatography. TG-MS was also utilized to evaluate the release of HBr from the modified fly ash and elucidate the mechanism for mercury capture.     

A rechargeable and portable hydrogen storage system grounded on soda water

The bicarbonate-formate（HCO^-₃– HCO^-₂） interconversion provides a promising cycle for a conveniently accessible hydrogen storage system via reversible dehydrogenation and hydrogenation processes. Existing catalytic systems often use organic solvents, tedious optimization as well as manipulation of pH values,solvent, pressure and various additives. Herein, we present an operational, robust, safe and cost-effective catalytic system for hydrogen storage and liberation. We have established a unique catalytic system with two different solid organometallic assemblies（NHC-Ru and NHC-Ir） that facilitate the reversible transformation between sodium formate and bicarbonate in aqueous solutions collaboratively and efficiently. Notably, the NHC-Ru catalyst is privileged for the hydrogenation of sodium bicarbonate, whereas the NHC-Ir component enables the dehydrogenation of sodium formate, all in a single reaction vessel. What sets this system apart is its simplicity. The H₂discharging and recharging is simply regulated by heating the mixture with or without H₂. Remarkably, this process requires no extra additives or supplementary treatments. Moreover, the reversible hydrogen storage system is durable and can be reused for over 30 cycles without a discernible decline in activity and selectivity. The strategic paradigm in this study shows significant practical potential in hydrogen fuel cell applications.     

Sampling and storage of materials for trace elemental analysis

Accurate analysis depends upon a valid, representative and uncontaminated analytical sample. For many trace metals, contamination overwhelms the sample, leading to inaccurate analytical data. Methods of controlling contamination and their implications for better methods of sampling and storage are discussed here.     

Correlation between composition and hydrogen storage behaviors of the Li2NH-MgNH combination system

Hydrogen storage performances of a Li(2)NH-xMgNH combination system (x = 0, 0.5, 1 and 2) are investigated for the first time. It is found that the hydrogenated samples with MgNH exhibit a significant reduction in the dehydrogenation temperatures. Mechanistic investigations reveal that there is a strong dependence of the hydrogen storage reaction process on the molar ratio between MgNH and Li(2)NH. As a consequence, tuning of thermodynamics is achieved for hydrogen storage in the Li(2)NH-xMgNH system by changing the reaction routes, which is ascertained to be the primary reason for the reduction in the operating temperature for hydrogen desorption. Specifically, it is found that under 105 atm hydrogen (140-280 °C) 5.6 wt% hydrogen is reversibly stored in the Li(2)NH-0.5MgNH combination system, which is greater than in the well-investigated Mg(NH(2))(2)-2LiH system.     

Computational analysis of amine-borane adducts as potential hydrogen storage materials with reversible hydrogen uptake

Amine-borane adducts are promising compounds for use in hydrogen storage applications, and the efficient catalytic release of hydrogen from these systems has been recently demonstrated. However, if hydrogen storage is to be of practical use, it is necessary that, once hydrogen has been removed from the material, it can be put back into the system to recharge the appliance. In order to develop such systems, we computationally screened a range of amine-borane adducts for their thermodynamic dehydrogenation properties. Structural trends, which lay the foundation for the possible design of amine-borane systems that exhibit reversible dihydrogen uptake, are established. We found that it is mainly the strengths of the dative bonds in both starting materials and products that govern the thermodynamic parameters of the dehydrogenation reactions. Thus, in general, electron-donating groups on nitrogen and electron-withdrawing groups on boron lead to more favorable systems. It is also possible to design promising systems whose thermodynamic parameters are a consequence of different steric strain in starting materials and products.     

Combined hydrogen production and storage with subsequent carbon crystallization

We provide evidence of low-temperature hydrogen evolution and possible hydrogen trapping in an anthracite coal derivative, formed via reactive ball milling with cyclohexene. No molecular hydrogen is added to the process. Raman-active molecular hydrogen vibrations are apparent in samples at atmospheric conditions (300 K, 1 bar) for samples prepared 1 year previously and stored in ambient air. Hydrogen evolves slowly at room temperature and is accelerated upon sample heating, with a first increase in hydrogen evolution occurring at approximately 60 degrees C. Subsequent chemical modification leads to the observation of crystalline carbons, including nanocrystalline diamond surrounded by graphene ribbons, other sp2-sp3 transition regions, purely graphitic regions, and a previously unidentified crystalline carbon form surrounded by amorphous carbon. The combined evidence for hydrogen trapping and carbon crystallization suggests hydrogen-induced crystallization of the amorphous carbon materials, as metastable hydrogenated carbons formed via the high-energy milling process rearrange into more thermodynamically stable carbon forms and molecular hydrogen.     

Laser-microprobe elemental determinations with an optical multichannel detection system

The results obtained when a laser microprobe is adapted to imaging detectors for multiwavelength detection are described. Detectors evaluated are a silicon-intensified target vidicon and a second-generation photodiode array. Data are presented to illustrate how the combined system can be used to monitor both surface and depth profiles of elemental content of a variety of sample types including a ruby rod and ceramic material with blemishes, electrical capacitors, integrated circuits, and surface-coated electrical conductors. It is also shown how the gating capability of the intensified vidicon can be used to monitor time-dependent changes in the several nanosecond range during the laser microprobe excitation process. Detection limits obtained with both detectors are in the range 2–500 ppm depending on the element, the wavelength used, the matrix, and other variables. The uncertainty associated with the measurement step can be improved by a factor of 2–3 by using ratios of spectral lines. Principal limitations of the laser microprobe method are the nonlinear response of intensity vs. concentration and the resulting need for reference materials with matrices similar to samples for calibration purposes.     

Development of amidoboranes for hydrogen storage

With high hydrogen content and moderate dehydrogenation conditions, metal amidoboranes have been regarded as potential hydrogen storage candidates and have attracted increasing attention recently. In this review we provide a practical introduction to the recent progress on the syntheses, crystal structures and dehydrogenation properties of metal amidoboranes and their derivatives.     

Thermodynamics study of hydrogen storage materials

The growing use of conventional energy such as fossil fuels results in problems degrading our environment. Hydrogen is frequently discussed as a clean energy in the future without pollution. However, efficient and safe storage of hydrogen constitute a key challenge and unresolved problem. One of the main options is solid-state storage technology. A successful solid-state reversible storage material should meet the requirements of high storage capacity, suitable thermodynamic properties, reversibility and fast adsorption and desorption kinetics. This feature article focuses mainly on the development of thermodynamic improvement of hydrogen storage materials in the past few years including the complex hydride, ammonia borane, and metal-organic frameworks.     

Quantitative estimation of NH3 partial pressure in H2 desorbed from the Li-N-H system by Raman spectroscopy

The partial pressure of NH3 gas estimated by Raman spectroscopy indicates that approximately 0.1% NH3 inevitably contaminates the H2 desorbed from a hydrogen storage material composed of LiH and LiNH2 at any temperature up to 400 degrees C in a closed system.     

Microbial reduction of sulfur dioxide with pretreated sewage sludge and elemental hydrogen as electron donors

It has been demonstrated that heat- and alkali-pretreated sewage sludge may serve as an electron donor and carbon source for SO₂ reduction byDesulfovibrio desulfuricans. A continuousD. desulfuricans culture was operated for 6 mo with complete reduction of SO₂ to H₂S. The culture required only minor amounts of mineral nutrients in addition to pretreated sewage sludge. It has also been shown that the sulfate-reducing bacteriumDesulfotomaculum orientis can be grown on H₂ as an energy source, CO₂ as a carbon source, and SO₂ as a terminal electron acceptor. Complete reduction of SO₂ to H₂S was observed.     

A single-component liquid-phase hydrogen storage material

The current state-of-the-art for hydrogen storage is compressed H(2) at 700 bar. The development of a liquid-phase hydrogen storage material has the potential to take advantage of the existing liquid-based distribution infrastructure. We describe a liquid-phase hydrogen storage material that is a liquid under ambient conditions (i.e., at 20 °C and 1 atm pressure), air- and moisture-stable, and recyclable; releases H(2) controllably and cleanly at temperatures below or at the proton exchange membrane fuel cell waste-heat temperature of 80 °C; utilizes catalysts that are cheap and abundant for H(2) desorption; features reasonable gravimetric and volumetric storage capacity; and does not undergo a phase change upon H(2) desorption.     

基于绿色氢科学理念构筑从低碳制氢到高效储氢的氢能体系

本文从低碳制氢和高效储氢的角度思考及探讨氢能体系绿色化发展过程中的关键科学问题.提出＂绿色氢科学＂理念与＂低碳制氢,高效储氢＂技术发展路线图,以期通过相关科学问题的认识,来构建具有高度原子经济性及可持续性的绿色氢能体系.     

Regeneration of copper(II) oxide with hydrogen gas in the reduction column of an elemental analyzer

Nitrogen in organic samples may be determined on a routine basis after combustion in elemental analyzer instruments. If elementary copper is used in the reduction column, it will be oxidized to copper(II) oxide by passing oxygen and nitrogen oxides. Instead of changing the reduction column it is possible to regenerate the copper(II) oxide to elemental copper with hydrogen gas without removing the column from the oven. A modification of the original instrument and procedure is described. In this method, the capacity of the column will decrease after regeneration, but time and chemical costs will be saved.     

Application of clathrate compounds for hydrogen storage

The review considers current works on clathrate hydrogen compounds, aimed at creating hydrogen accumulators suitable for practical application. Analysis of published data showed that clathrate hydrates formed by pure hydrogen are unsuitable for this purpose in view of their fairly low limiting hydrogen content and the necessity for their synthesis of extremely high pressures (>100 MPa) that are still industrially unfeasible. The possibilities for hydrogen storage in double (including auxiliary guest molecules along with hydrogen) clathrate hydrates are considered. It is concluded from published data that sorbents on the basis of the so-called “metal-organic frameworks” (MOFs) with a pore size of 1–2 nm hold a greater promise for hydrogen storage at temperatures of about 100 and moderately (up to 10 MPa) high pressures, but the development of all the considered methods of hydrogen storage has not yet grown out of laboratory experiments.