RESUMEN
The effect of the partial substitution of Mo with W in Co3 Mo3 N and Ni2 Mo3 N on ammonia synthesis activity and lattice nitrogen reactivity has been investigated. This is of interest as the coordination environment of lattice N is changed by this process. When tungsten was introduced into the metal nitrides by substitution of Mo atoms, the catalytic performance was observed to have decreased. As expected, Co3 Mo3 N was reduced to Co6 Mo6 N under a 3 : 1 ratio of H2 /Ar. Co3 Mo2.6 W0.4 N was also shown to lose a large percentage of lattice nitrogen under these conditions. The bulk lattice nitrogen in Ni2 Mo3 N and Ni2 Mo2.8 W0.2 N was unreactive, demonstrating that substitution with tungsten does not have a significant effect on lattice N reactivity. Computational calculations reveal that the vacancy formation energy for Ni2 Mo3 N is more endothermic than Co3 Mo3 N. Furthermore, calculations suggest that the inclusion of W does not have a substantial impact on the surface N vacancy formation energy or the N2 adsorption and activation at the vacancy site.
RESUMEN
Ammonia (NH3) synthesis is an essential yet energy-demanding industrial process. Hence, there is a need to develop NH3 synthesis catalysts that are highly active under milder conditions. Metal nitrides are promising candidates, with the η-carbide Co3Mo3N having been found to be more active than the industrial Fe-based catalyst. The isostructural Fe3Mo3N catalyst has also been identified as highly active for NH3 synthesis. In the present work, we investigate the catalytic ammonia synthesis mechanisms in Fe3Mo3N, which we compare and contrast with the previously studied Co3Mo3N. We apply plane-wave density functional theory (DFT) to investigate surface N vacancy formation in Fe3Mo3N, and two distinct ammonia synthesis mechanisms. The calculations reveal that whilst N vacancy formation on Fe3Mo3N is more thermodynamically demanding than for Co3Mo3N, the formation energies are comparable, suggesting that surface lattice N vacancies in Fe3Mo3N could facilitate NH3 synthesis. N2 activation was found to be enhanced on Fe3Mo3N compared to Co3Mo3N, for adsorption both at and adjacent to the vacancy. The calculated activation barriers suggest that, as for Co3Mo3N, the associative Mars van Krevelen mechanism affords a much less energy-demanding pathway for ammonia synthesis, especially for initial hydrogenation processes.
RESUMEN
The ammonia synthesis activities of the anti-perovskite nitrides Co3CuN and Ni3CuN have been compared to investigate the possible metal composition-activity relationship. Post-reaction elemental analysis showed that the activity for both nitrides was due to loss of lattice nitrogen rather than a catalytic process. Co3CuN was observed to convert a higher percentage of lattice nitrogen to ammonia than Ni3CuN and was active at a lower temperature. The loss of lattice nitrogen was revealed to be topotactic and Co3Cu and Ni3Cu were formed during the reaction. Therefore, the anti-perovskite nitrides may be of interest as reagents for the formation of ammonia through chemical looping. The regeneration of the nitrides was achieved by ammonolysis of the corresponding metal alloys. However, regeneration using N2 was shown to be challenging. In order to understand the difference in reactivity between the two nitrides, DFT techniques were applied to investigate the thermodynamics of the processes involved in the evolution of lattice nitrogen to the gas phase via conversion to N2 or NH3, revealing key differences in the energetics of bulk conversion of the anti-perovskite to the alloy phase, and in loss of surface N from the stable low-index N-terminated (111) and (100) facets. Computational modelling of the density of states (DOS) at the Fermi level was performed. It was shown that the Ni and Co d states contributed to the density of states and that the Cu d states only contributed to the DOS for Co3CuN. The anti-perovskite Co3MoN has been investigated as comparisons with Co3Mo3N may give an insight into the role structure type plays in the ammonia synthesis activity. The XRD pattern and elemental analysis for the synthesised material revealed that an amorphous phase was present that contained nitrogen. In contrast to Co3CuN and Ni3CuN, the material was shown to have steady state activity at 400 °C with a rate of 92 ± 15 µmol h-1 g-1. Therefore, it appears that metal composition has an influence on the stability and activity of the anti-perovskite nitrides.
RESUMEN
In this review, we present the recent progress in ammonia synthesis research using density functional theory (DFT) calculations on various industrial catalysts, metal nitrides and nano-cluster-supported catalysts. The mechanism of ammonia synthesis on the industrial Fe catalyst is generally accepted to be a dissociative mechanism. We have recently found, using DFT techniques, that on Co3Mo3N (111) surfaces, an associative mechanism in the synthesis of ammonia can offer a new low-energy pathway that was previously unknown. In particular, we have shown that metal nitrides that are also known to have high activity for ammonia synthesis can readily form nitrogen vacancies which can activate dinitrogen, thereby promoting the associative mechanism. These fundamental studies suggest that a promising route to the discovery of low-temperature ammonia synthesis catalysts will be to identify systems that proceed via the associative mechanism, which is closer to the nitrogen-fixation mechanism occurring in nitrogenases.
RESUMEN
In this study, the process economics of ammonia synthesis over Co3Mo3N was investigated by searching for an optimum feed stoichiometry. From ammonia synthesis rate measurements at atmospheric pressure and 400 °C over Co3Mo3N, it was found that the rate was independent of H2 : N2 stoichiometry for stoichiometries above 0.5 : 1. For H2 : N2 stoichiometries below 0.5 : 1, there was a linear dependency of ammonia synthesis rate on the H2 : N2 stoichiometry. Static measurements of hydrogen adsorption isotherms at 25, 50, and 100 °C revealed that the adsorbed amounts of strongly bound hydrogen over the Co3Mo3N surface were saturated at around 100 Torr hydrogen pressure. This pressure corresponds to the partial pressure of hydrogen when the H2 : N2 stoichiometry is around 0.5 : 1, confirming the role of strongly bound hydrogen in ammonia synthesis. These results were used to modify an existing kinetic expression to be used in a conceptual design, based on a late mixing strategy for the hydrogen stream. This conceptual design and its economic analysis revealed that using low hydrogen stoichiometries can cut the investment and operating costs by a factor of 2.
RESUMEN
Manganese nitride related materials are of interest as two-stage reagents for ammonia synthesis via nitrogen chemical looping. However, unless they are doped with a co-cation, manganese nitrides are thermochemically stable and a high temperature is required to produce ammonia under reducing conditions, thereby hindering their use as nitrogen transfer materials. Nevertheless, when lithium is used as dopant, ammonia generation can be observed at a reaction temperature as low as 300 °C. In order to develop strategies for the improvement of the reactivity of nitride materials in the context of two-stage reagents, it is necessary to understand the intrinsic role of the dopant in the mechanism of ammonia synthesis. To this end, we have investigated the role of lithium in increasing the manganese nitride reactivity by in situ neutron diffraction studies and N2 and H2 isotopic exchange reactions supplemented by DFT calculations.
RESUMEN
The implementation of ammonia as a hydrogen vector relies on the development of active catalysts to release hydrogen on-demand at low temperatures. As an alternative to ruthenium-based catalysts, herein we report the high activity of silica aerogel supported cobalt rhenium catalysts. XANES/EXAFS studies undertaken at reaction conditions in the presence of the ammonia feed reveal that the cobalt and rhenium components of the catalyst which had been pre-reduced are initially re-oxidised prior to their subsequent reduction to metallic and bimetallic species before catalytic activity is observed. A synergistic effect is apparent in which this re-reduction step occurs at considerably lower temperatures than for the corresponding monometallic counterpart materials. The rate of hydrogen production via ammonia decomposition was determined to be 0.007 molH2 gcat-1 h-1 at 450 °C. The current study indicates that reduced Co species are crucial for the development of catalytic activity.
RESUMEN
Single phase solid solutions based on copper and iron substitution into the nickel sites of Ni2Mo3N are produced using a citrate gel approach followed by ammonolysis. These metal nitrides show good ammonia synthesis activity at 500 °C and ambient pressure. The activity fell with copper content and increased with iron content, although these changes appear to be related to the surface areas of the catalysts. The oxide intermediates from the citrate gel process cleanly converted to the metal nitride under the ammonia synthesis gas stream (75% H2, 25% N2) providing more active catalysts than those pre-nitrided by ammonolysis.
RESUMEN
In this perspective we present recent experimental and computational progress in catalytic ammonia synthesis research on metal nitrides involving a combined approach. On this basis, it suggested that the consideration of nitrogen vacancies in the synthesis of ammonia can offer new low energy pathways that were previously unknown. We have shown that metal nitrides that are also known to have high activity for ammonia synthesis can readily form nitrogen vacancies on their surfaces. These vacancies adsorb dinitrogen much more strongly than the defect-free surfaces and can efficiently activate the strong N-N triple bond. These fundamental studies suggest that heterogeneously catalysed ammonia synthesis over metal nitrides is strongly affected by bulk and surface defects and that further progress in the discovery of low temperature catalysts relies on more careful consideration of nitrogen vacancies. The potential occurrence of an associative pathway in the case of the Co3Mo3N catalytic system provides a possible link with enzymatic catalysis, which will be of importance in the design of heterogeneous catalytic systems operational under process conditions of reduced severity which are necessary for the development of localised facilities for the production of more sustainable "green" ammonia.
RESUMEN
A cobalt rhenium catalyst active for ammonia synthesis at 400 °C and ambient pressure was studied using in situ XAS to elucidate the reducibility and local environment of the two metals during reaction conditions. The ammonia reactivity is greatly affected by the gas mixture used in the pre-treatment step. Following H2/Ar pre-treatment, a subsequent 20 min induction period is also observed before ammonia production occurs whereas ammonia production commences immediately following comparable H2/N2 pre-treatment. In situ XAS at the Co K-edge and Re LIII-edge show that cobalt initiates reduction, undergoing reduction between 225 and 300 °C, whereas reduction of rhenium starts at 300 °C. The reduction of rhenium is near complete below 400 °C, as also confirmed by H2-TPR measurements. A synergistic co-metal effect is observed for the cobalt rhenium system, as complete reduction of both cobalt and rhenium independently requires higher temperatures. The phases present in the cobalt rhenium catalyst during ammonia production following both pre-treatments are largely bimetallic Co-Re phases, and also monometallic Co and Re phases. The presence of nitrogen during the reduction step strongly promotes mixing of the two metals, and the bimetallic Co-Re phase is believed to be a pre-requisite for activity.
RESUMEN
The reactants for ammonia synthesis have been studied, employing density functional theory (DFT), with respect to their adsorption on tantalum nitride surfaces. The adsorption of nitrogen was found to be mostly molecular and non-activated with side-on, end-on and tilt configurations. At bridging nitrogen sites (Ta-N-Ta) it results in an azide functional group formation with a formation energy of 205 kJ mol-1. H2 was found also to chemisorb molecularly with an adsorption energy in the range -81 to -91 kJ mol-1. At bridging nitrogen sites it adsorbs dissociatively forming >NH groups with an exothermic formation energy of -175 kJ mol-1 per H2. The nitrogen vacancy formation energies were relatively high compared to other metal nitrides found to be 2.89 eV, 2.32 eV and 1.95 eV for plain, surface co-adsorbed cobalt and sub-surface co-adsorbed cobalt Ta3N5-(010). Co-adsorption of cobalt was found to occur mostly at nitrogen rich sites of the surface with an adsorption energy that ranged between -200 to -400 kJ mol-1. The co-adsorption of cobalt was found to enhance the dissociation of molecular hydrogen on the surface of Ta3N5. The studies offer significant new insight with respect to the chemistry of N2 and H2 with tantalum nitride surfaces in the presence of cobalt promoters.
RESUMEN
The co-ammonolysis of V(NMe2)4 and Si(NHMe)4 with ammonia in THF and in the presence of ammonium triflate ([NH4][CF3SO3]) leads to the formation of monolithic gels. Pyrolysing these gels produces mesoporous composite materials containing nanocrystalline VN and amorphous silicon imidonitride. Elemental mapping indicated a thorough distribution of VN with no evidence of large cluster segregation. Whilst not active for ammonia synthesis, the silicon nitride based materials were found to possess activity for the COx-free production of H2 from methane, which makes them candidates for applications in which the presence of low levels of CO in H2 feedstreams is detrimental.
RESUMEN
Reactions of Si(NHMe)4 with ammonia are effectively catalysed by small ammonium triflate concentrations, and can be used to produce free-standing silicon imide gels. Firing at various temperatures produces amorphous or partially crystallised silicon imidonitride/nitride samples with high surface areas and low oxygen contents. The crystalline phase is entirely α-Si3N4 and structural similarities are observed between the amorphous and crystallised materials.
RESUMEN
BACKGROUND: Iron ochres are gelatinous sludges that can cause problems in terms of water management. In this work, the application of iron ochre obtained from a river has been applied to catalytically crack methane - another potential waste product - into two useful products, hydrogen and a magnetic carbon-containing composite. RESULTS: The powder X-ray diffraction (XRD) pattern of the iron ochre was found to be consistent with the expected 2-line ferrihydrite, and energy dispersive X-ray (EDX) analysis showed Fe to be a major component although some Si and Ca were present. The sample was observed to contain a fraction with a tubular morphology consistent with the presence of extra-cellular biogenic iron oxide formed by leptothrix. Upon exposure to methane at elevated temperatures, the material was found to transform into an active catalyst for hydrogen production yielding a magnetic carbon-containing composite material comprising filamentous carbon and encapsulating graphite. CONCLUSION: The application of two waste products - iron ochre and methane - to generate two useful products - hydrogen and a magnetic carbon-containing composite - has been demonstrated. Furthermore, the ochre has been shown to comprise tubular morphology extra-cellular biogenic iron oxide which may be of interest in terms of other applications. © 2014 The Authors. Journal of Chemical Technology & Biotechnology published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.
RESUMEN
The 14N/15N isotopic exchange pathways over Co3Mo3N, a material of interest as an ammonia synthesis catalyst and for the development of nitrogen transfer reactions, have been investigated. Both the homomolecular and heterolytic exchange processes have been studied, and it has been shown that lattice nitrogen species are exchangeable. The exchange behavior was found to be a strong function of pretreatment with ca. 25% of lattice N atoms being exchanged after 40 min at 600 °C after N2 pretreatment at 700 °C compared to only 6% following similar Ar pretreatment. This observation, for which the potential contribution of adsorbed N species can be discounted, is significant in terms of the application of this material. In the case of the Co6Mo6N phase, regeneration to Co3Mo3N under 15N2 at 600 °C occurs concurrently with 14N15N formation. These observations demonstrate the reactivity of nitrogen in the Co-Mo-N system to be a strong function of pretreatment and worthy of further consideration.
