scholarly journals Synthesis of ammonia directly from wet air using Sm0.6Ba0.4Fe0.8Cu0.2O3−δ as the catalyst

2015 ◽  
Vol 182 ◽  
pp. 353-363 ◽  
Author(s):  
Rong Lan ◽  
Khaled A. Alkhazmi ◽  
Ibrahim A. Amar ◽  
Shanwen Tao

Ammonia was directly synthesised from wet air at 400 °C at atmospheric pressure. A new perovskite Sm0.6Ba0.4Fe0.8Cu0.2O3−δ was used as the electrocatalyst for electrochemical synthesis of ammonia. Ammonia formation rates of 9.19 × 10−7 mol s−1 m−2 and 1.53 × 10−6 mol s−1 m−2 were obtained at 400 °C when wet air and wet N2 were introduced into a simple single chamber reactor, respectively. The perovskite catalyst is low cost compared to the previously reported Ru/MgO and Pt/C catalysts. This experiment indicates that ammonia can be directly synthesised from wet air, a very promising simple technology for sustainable synthesis of ammonia in the future.

Author(s):  
Wenchao Lian ◽  
Mo Yingyu ◽  
Libin Lei ◽  
Yongzheng Ou ◽  
Ruiming Qiu ◽  
...  

Ammonia (NH3) as a carbon-free hydrogen carrier shows great potential as fuel and its production at mild conditions is desired. NH3 synthesis at atmospheric pressure can be realized in solid-state...


RSC Advances ◽  
2021 ◽  
Vol 11 (29) ◽  
pp. 17891-17900
Author(s):  
Chien-I. Li ◽  
Hiroki Matsuo ◽  
Junichiro Otomo

Electrochemical promotion of ammonia formation is mainly governed by surface reaction with N2 and H2 in the cathode.


1983 ◽  
Vol 74 (3) ◽  
pp. 607-610
Author(s):  
JJ ROUND ◽  
J ROBSON ◽  
DN BRADLEY ◽  
REB BARNARD ◽  
RA WILLIAMS ◽  
...  

Pharmaceutics ◽  
2021 ◽  
Vol 13 (8) ◽  
pp. 1186
Author(s):  
Carmen S. Favaro-Trindade ◽  
Fernando E. de Matos Junior ◽  
Paula K. Okuro ◽  
João Dias-Ferreira ◽  
Amanda Cano ◽  
...  

Nanoencapsulation via spray cooling (also known as spray chilling and spray congealing) has been used with the aim to improve the functionality, solubility, and protection of drugs; as well as to reduce hygroscopicity; to modify taste and odor to enable oral administration; and many times to achieve a controlled release profile. It is a relatively simple technology, it does not require the use of low-cost solvents (mostly associated to toxicological risk), and it can be applied for lipid raw materials as excipients of oral pharmaceutical formulations. The objective of this work was to revise and discuss the advances of spray cooling technology, with a greater emphasis on the development of lipid micro/nanoparticles to the load of active pharmaceutical ingredients for oral administration.


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