scholarly journals Promising Isotope Effect in Pd77Ag23 for Hydrogen Separation

2021 ◽  
Vol 5 (3) ◽  
pp. 51
Author(s):  
Francesco Trequattrini ◽  
Oriele Palumbo ◽  
Silvano Tosti ◽  
Alessia Santucci ◽  
Annalisa Paolone

Pd–Ag alloys are largely used as hydrogen separation membranes and, as a consequence, the Pd–Ag–H system has been intensively studied. On the contrary, fewer information is available for the Pd–Ag–D system; thus, the aim of this work is to improve the knowledge of the isotope effect on the commercial Pd77Ag23 alloy, especially for temperature above 200 °C. In particular, deuterium absorption measurements are carried out in the Pd77Ag23 alloy in the temperature range between 79 and 400 °C and in the pressure range between 10−2 and 16 bar. In this exploited pressure (p) and composition (c) range, above 300 °C the pc isotherms display the typical shape of materials where only a solid solution of deuterium is present while at lower temperatures these curves seem to be better described by the coexistence of a solid solution and a deuteride in a large composition range. The obtained results are compared and discussed with the ones previously measured with the lightest hydrogen isotope. Such a comparison shows that the Pd77Ag23 alloy exhibits a clear inverse isotope effect, as the equilibrium pressure of the Pd–Ag–D system is higher than in Pd–Ag–H by a factor of ≈2 and the solubility of deuterium is about one half of that of hydrogen. In addition, the absorption measurements were used to assess the deuteration enthalpy that below 300 °C is ΔHdeut = 31.9 ± 0.3 kJ/mol, while for temperatures higher than 300 °C, ΔHdeut increases to 43 ± 1 kJ/mol. Additionally, in this case a comparison with the lighter isotope is given and both deuteration enthalpy values result lower than those reported for hydrogenation. The results described in this paper are of practical interest for applications operating above 200 °C, such as membranes or packing column, in which Pd77Ag23 has to interact with a gas stream containing both hydrogen isotopes.

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Paul M. Magyar ◽  
Damian Hausherr ◽  
Robert Niederdorfer ◽  
Nicolas Stöcklin ◽  
Jing Wei ◽  
...  

AbstractAnaerobic ammonium oxidation (anammox) plays an important role in aquatic systems as a sink of bioavailable nitrogen (N), and in engineered processes by removing ammonium from wastewater. The isotope effects anammox imparts in the N isotope signatures (15N/14N) of ammonium, nitrite, and nitrate can be used to estimate its role in environmental settings, to describe physiological and ecological variations in the anammox process, and possibly to optimize anammox-based wastewater treatment. We measured the stable N-isotope composition of ammonium, nitrite, and nitrate in wastewater cultivations of anammox bacteria. We find that the N isotope enrichment factor 15ε for the reduction of nitrite to N2 is consistent across all experimental conditions (13.5‰ ± 3.7‰), suggesting it reflects the composition of the anammox bacteria community. Values of 15ε for the oxidation of nitrite to nitrate (inverse isotope effect, − 16 to − 43‰) and for the reduction of ammonium to N2 (normal isotope effect, 19–32‰) are more variable, and likely controlled by experimental conditions. We argue that the variations in the isotope effects can be tied to the metabolism and physiology of anammox bacteria, and that the broad range of isotope effects observed for anammox introduces complications for analyzing N-isotope mass balances in natural systems.


2012 ◽  
Vol 37 (1) ◽  
pp. 894-902 ◽  
Author(s):  
Jianjun Ye ◽  
Jian Yang ◽  
Jinyang Zheng ◽  
Xianting Ding ◽  
Ieong Wong ◽  
...  

2021 ◽  
Author(s):  
Wei Liu ◽  
Ming Yang ◽  
Jing Liu ◽  
Meijia Yang ◽  
Jing Li ◽  
...  

Abstract The unique magnetic, electronic and optical features derived from their unpaired electrons have made radical polymers an attractive material platform for various applications. Here, we report solution-processable radical polymer membranes with multi-level porosities and study the impact of free radicals on important membrane separation processes including solar vapor generation, hydrogen separation and CO2 capture. The radical polymer is a supreme light absorber over the full solar irradiation range with sufficient water transport channels, leading to a highly efficient solar evaporation membrane. In addition, the radical polymer with micropores and adjustable functional groups are broad-spectrum gas separation membranes for both hydrogen separation and CO2 capture. First principle calculations indicate that the conjugated polymeric network bearing radicals is more chemically reactive with CO2, compared with H2, N2 and CH4. This is evidenced by a high CO2 permeability in gas separation membranes made of the conjugated radical polymer.


ACS Catalysis ◽  
2019 ◽  
Vol 9 (3) ◽  
pp. 2657-2663 ◽  
Author(s):  
Ying Zhang ◽  
Malkanthi K. Karunananda ◽  
Hsien-Cheng Yu ◽  
Kyle J. Clark ◽  
Wendy Williams ◽  
...  

2001 ◽  
Vol 120 (1-3) ◽  
pp. 713-714 ◽  
Author(s):  
Aravinda M. Kini ◽  
John A. Schlueter ◽  
Brian H. Ward ◽  
Urs W. Geiser ◽  
H.Hau Wang

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