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Ammonia

About: Ammonia is a research topic. Over the lifetime, 16217 publications have been published within this topic receiving 271940 citations. The topic is also known as: NH3 & azane.


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Journal ArticleDOI
TL;DR: In this article, the authors demonstrate how ammonia can be produced at ambient pressure from air, water, and concentrated sunlight as renewable source of process heat via nitrogen reduction with a looped metal nitride, followed by separate hydrogenation of the lattice nitrogen into ammonia.
Abstract: The activity of many heterogeneous catalysts is limited by strong correlations between activation energies and adsorption energies of reaction intermediates. Although the reaction is thermodynamically favourable at ambient temperature and pressure, the catalytic synthesis of ammonia (NH3), a fertilizer and chemical fuel, from N2 and H2 requires some of the most extreme conditions of the chemical industry. We demonstrate how ammonia can be produced at ambient pressure from air, water, and concentrated sunlight as renewable source of process heat via nitrogen reduction with a looped metal nitride, followed by separate hydrogenation of the lattice nitrogen into ammonia. Separating ammonia synthesis into two reaction steps introduces an additional degree of freedom when designing catalysts with desirable activation and adsorption energies. We discuss the hydrogenation of alkali and alkaline earth metal nitrides and the reduction of transition metal nitrides to outline a promoting role of lattice hydrogen in ammonia evolution. This is rationalized via electronic structure calculations with the activity of nitrogen vacancies controlling the redox-intercalation of hydrogen and the formation and hydrogenation of adsorbed nitrogen species. The predicted trends are confirmed experimentally with evolution of 56.3, 80.7, and 128 μmol NH3 per mol metal per min at 1 bar and above 550 °C via reduction of Mn6N2.58 to Mn4N and hydrogenation of Ca3N2 and Sr2N to Ca2NH and SrH2, respectively.

149 citations

Journal ArticleDOI
TL;DR: The relatively greater decrease in ammonia nitrogen excretion over total ammonia excretion in fish exposed to the higher concentrations of ammonia suggests that excretion of other nitrogenous compounds occured to partially compensate for the significant decrease in nitrogen excreted by these fish.

148 citations

Journal ArticleDOI
TL;DR: A transient augmentation of the rate of ammonia excretion is observed upon acidification, suggesting an increased permeability of the gill to the free-base form of ammonia.
Abstract: 1. Sodium exchange, ammonia excretion and H + ion movement across the gill were measured in sodium-depleted Carassius auratus . Sodium uptake and ammonia excretion are considerably enhanced by sodium depletion. In this respect sodium-depleted fish behave as ammonia-loaded fish. 2. A decrease of the external pH by one unit results in a 50-60% decrease in both influx and efflux of sodium. A transient augmentation of the rate of ammonia excretion is observed upon acidification, suggesting an increased permeability of the gill to the free-base form of ammonia. 3. The ionic balance sheet of the movements of the monovalent ions across the gill was drawn up when a permeant co-ion for sodium was absent from the external medium. In both acid and alkaline media the ionic balance was achieved in accordance with the law of electroneutrality of external and internal solutions. 4. Net Na + uptake was only found to be correlated to NH 4 + excretion if H + ion movements across the gill were taken into account. 5. Ammonia-gradient experiments were performed to test the ability of the gill to excrete ammonia against a gradient of ammonia partial pressure. Ammonia excretion is independent of this gradient in alkaline media when sodium ions are present. In these conditions ammonia moves in the ionic form. In acid media, with Na present in the external medium, ammonia movement is correlated with the p NH 3 gradient but uphill movement still occurs. Ammonia moves in both the free-base and the ionized forms. In the absence of external sodium, movements of ammonia obey the law for passive transfer and ammonia moves exclusively in the free-base form, even though the external medium is alkaline.

148 citations

Journal ArticleDOI
TL;DR: This novel approach holds promise for selective recovery of nitrogen from concentrated liquid waste streams such as source-separated urine using electrochemical stripping, a combination of electrodialysis and membrane stripping.
Abstract: Recovering nitrogen from separately collected urine can potentially reduce costs and energy of wastewater nitrogen removal and fertilizer production. Through benchtop experiments, we demonstrate the recovery of nitrogen from urine as ammonium sulfate using electrochemical stripping, a combination of electrodialysis and membrane stripping. Nitrogen was selectively recovered with 93% efficiency in batch experiments with real urine and required 30.6 MJ kg N–1 in continuous-flow experiments (slightly less than conventional ammonia stripping). The effects of solution chemistry on nitrogen flux, electrolytic reactions, and reactions with electro-generated oxidants were evaluated using synthetic urine solutions. Fates of urine-relevant trace organic contaminants, including electrochemical oxidation and reaction with electro-generated chlorine, were investigated with a suite of common pharmaceuticals. Trace organics (<0.1 μg L–1) and elements (<30 μg L–1) were not detected at appreciable levels in the ammonium su...

148 citations

Journal ArticleDOI
TL;DR: In this article, the interaction of NO, ammonia (NH3), hydrazine (N2H4), hydroxylamine (NH2OH), urea (H2N), acetamide (CH3), and acetonitrile (CH 3CN) on Fe2O3-TiO2 model catalysts was studied.
Abstract: The interaction of NO, ammonia (NH3), hydrazine (N2H4), hydroxylamine (NH2OH), urea (H2NCONH2), acetamide (CH3CONH2) and acetonitrile (CH3CN) on Fe2O3-TiO2 model catalysts was studied. The data support the idea that hydrazine can be intermediate in the oxidation of ammonia to nitrogen, while hydroxylamine-type species, formed at higher temperature, can be intermediate in the oxidation of ammonia to NO. Bronsted acid sites do not appear to be involved in this chemistry.

148 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
20231,701
20223,035
2021425
2020443
2019496
2018511