2020
DOI: 10.1016/j.fuel.2020.118372
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Highly active Pd catalysts supported on surface-modified cobalt-nickel mixed oxides for low temperature oxidation of lean methane

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Cited by 31 publications
(24 citation statements)
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“…22 The peaks at a binding energy of ∼533.0 eV corresponded to the surface hydroxyl (O OH ) species. 27 The quantitative results of the O 1s spectra are shown in Tables 2 and S2. The peak located at 533.0 eV occupied an important part (0.23) in the spectrum of NiO-NSL, whereas the content of the hydroxyl groups on the other samples was negligible.…”
Section: Activity Determination and Specific Reactionmentioning
confidence: 99%
“…22 The peaks at a binding energy of ∼533.0 eV corresponded to the surface hydroxyl (O OH ) species. 27 The quantitative results of the O 1s spectra are shown in Tables 2 and S2. The peak located at 533.0 eV occupied an important part (0.23) in the spectrum of NiO-NSL, whereas the content of the hydroxyl groups on the other samples was negligible.…”
Section: Activity Determination and Specific Reactionmentioning
confidence: 99%
“…Consequently, O 2 -TPD experiments (Figure S3B) were conducted to understand the oxygen activities of HfO 2 -related samples inspired by the discussion of H 2 -TPR results. In general, the desorption of surface-adsorbed oxygen occurs at temperatures below 400 °C, 43 identical to the temperature window of the methane combustion reaction, and lattice oxygen would release from the bulk domain of catalyst materials at higher temperatures. The more intensive liberation of O ads species in 1.0Pd/HfO 2 and 1.0Pd/mod-HfO 2 compared to their HfO 2 and mod-HfO 2 supports, which was in agreement with the conclusion drawn from O 1s XPS spectra, confirmed that the deposition of palladium could enhance the activation of oxygen species.…”
Section: Resultsmentioning
confidence: 99%
“…29,30 This is often accomplished by tuning the optimal amount of Pd x+ surface species (0≤x≤4) which are stabilized on the surface and subsurface region based on reaction conditions, surface dopants and support type. [31][32][33][34] We previously reported a novel solvent-free mechano-chemical route for the synthesis of highly active methane oxidation Pd/CeO2 catalysts starting from either metallic Pd nanopowders or Pd salts. 35,36 The developed synthesis procedure resulted in catalytic materials with a peculiar coreshell morphology, displaying enhanced methane oxidation activity at low and high temperature and improved stability in the presence of excess steam.…”
Section: Introductionmentioning
confidence: 99%
“…Currently, it accounts for the major contribution to CH 4 release in optimized aftertreatment systems since the stable nature of the CH 4 molecule (C–H bond energy = 439 kJ/mol) hinders its low temperature abatement . Several approaches have been considered to reduce its ignition delay, including innovative design of the reactor setup for faster heating and optimization of the Pd active phase for CH 4 activation at lower temperature. , This is often accomplished by tuning the optimal amount of Pd x + surface species (0 ≤ x ≤ 4) which are stabilized on the surface and subsurface region based on reaction conditions, surface dopants, and support type. …”
Section: Introductionmentioning
confidence: 99%