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@INPROCEEDINGS{AzuaHumara:1034907,
author = {Azua Humara, Ana Daniela and Luna Barron, Ana Laura and
Mechler, Anna and Eichel, Rüdiger-A.},
title = {{U}nderstanding {N}itrate {E}lectrochemical {R}eduction to
{A}mmonia by {I}dentifying {C}hanges in p{H}},
school = {RWTH Aachen},
reportid = {FZJ-2025-00028},
year = {2024},
abstract = {Electrochemical nitrate reduction into ammonia is an
attractive technology that promotes nitrates removal from
wastewater while delivering ammonia as a profitable
product.[1] Electrochemical nitrates S reduction to ammonia
in aqueous media under ambient conditions has been reported,
using noble metal-based electrodes (e.g., Ru, Rh, Pt). [2]
It has been shown that the nitrates reduction is a complex
process due to its polyatomic nature, forming several
intermediate compounds before its complete reduction into
ammonia. The ammonia selectivity depends on the
electrocatalyst, the applied potential, and the electrolyte
media. [3] Jaramillo’s group studied the effect of the
initial pH electrolyte on the ammonia Faradaic efficiency,
concluding ammonia formation is favored at low pH (<1).[1]
Clearly, pH plays an essential role in nitrates reduction.
However, there is limited knowledge of pH changes through
the reaction, since only initial pH is reported, and how and
why such changes impact the ammonia selectivity. In this
work, the changes in pH during the electrochemical reduction
of nitrates to ammonia are evaluated using Ti and Cu-foils.
We investigate four different electrolytes ranging from pH 1
to pH 10, tracking the changes in pH over the course of a 30
min experiment. Our results show that when the initial pH is
equal to or above pH 3 the media undergoes alkalinization,
reaching pH values close to 12. On the other hand, in acidic
conditions the pH only increases slightly. In addition, the
highest faradaic efficiency is obtained at more alkaline
initial conditions. The intermediate products are also
detected and correlated to the pH increase.},
month = {Sep},
date = {2024-09-16},
organization = {Gesellschaft Deutscher Chemiker -
Electrochemistry 2024, Braunschweig
(Germany), 16 Sep 2024 - 19 Sep 2024},
subtyp = {After Call},
cin = {IET-1},
cid = {I:(DE-Juel1)IET-1-20110218},
pnm = {1231 - Electrochemistry for Hydrogen (POF4-123) / HITEC -
Helmholtz Interdisciplinary Doctoral Training in Energy and
Climate Research (HITEC) (HITEC-20170406) / BMBF 03SF0589B -
Verbundvorhaben iNEW: Inkubator Nachhaltige Elektrochemische
Wertschöpfungsketten (iNEW) im Rahmen des Gesamtvorhabens
Accelerator Nachhaltige Bereitstellung Elektrochemisch
Erzeugter Kraft- und Wertstoffe mittels Power-to-X (ANABEL)
(03SF0589B)},
pid = {G:(DE-HGF)POF4-1231 / G:(DE-Juel1)HITEC-20170406 /
G:(BMBF)03SF0589B},
typ = {PUB:(DE-HGF)24},
url = {https://juser.fz-juelich.de/record/1034907},
}