2015
DOI: 10.1016/j.comptc.2015.04.011
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Theoretical study of catalytic decomposition of acetic acid on MgO nanosurface

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Cited by 10 publications
(9 citation statements)
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“…Takahashi et al 12 reported that the deep level defects in MgO are usually created by impurities and vacancy complexes lie in 1.4-4.6 eV. Perera et al 13 found that this band can be present in MgO microcrystals and centered at 2.8 eV. These authors have associated the above bands to Mg interstates.…”
Section: Photoluminescence Spectramentioning
confidence: 98%
“…Takahashi et al 12 reported that the deep level defects in MgO are usually created by impurities and vacancy complexes lie in 1.4-4.6 eV. Perera et al 13 found that this band can be present in MgO microcrystals and centered at 2.8 eV. These authors have associated the above bands to Mg interstates.…”
Section: Photoluminescence Spectramentioning
confidence: 98%
“…CO 2 was the predominant gas compound when using the NiWHZ catalyst (36.6 wt %), formed as an end product of decarboxylation of acetic acid, which catalytically decomposes releasing CO 2 and CH 4 through a competitive decarboxylation−dehydration mechanism. 37,52 On the other hand, given the lower activity of the CoMoHZ catalyst, the concentration of CH 4 (24.2 vol %) surpasses that of CO and CO 2 , indicating that less oxygen is being removed during HDO using this catalyst. Details on the total coke content and CK/TL ratios (as obtained from the deconvolution of the DTG−TPO curves in Figure S2) are provided in Figure 1c.…”
Section: ■ Resultsmentioning
confidence: 99%
“…The composition of the main gas products in Figure b reveals a significant concentration of CO and CO 2 (36.9 vol % and 25.3 vol %, respectively) using the PtPdHZ catalyst, which originate from decarbonylation (CO) and decarboxylation (CO 2 ) reactions, mostly. CO 2 was the predominant gas compound when using the NiWHZ catalyst (36.6 wt %), formed as an end product of decarboxylation of acetic acid, which catalytically decomposes releasing CO 2 and CH 4 through a competitive decarboxylation–dehydration mechanism. , On the other hand, given the lower activity of the CoMoHZ catalyst, the concentration of CH 4 (24.2 vol %) surpasses that of CO and CO 2 , indicating that less oxygen is being removed during HDO using this catalyst.…”
Section: Resultsmentioning
confidence: 99%
“…1.94% weight loss upon heating from room temperature to 165°C, which is due to the removal of adsorbed water on the surface of the product. e weight loss from 165°C to 500°C may be ascribed to the decomposition of the CH 3 COO − and NO 3 − anions, as the acetate and nitrate anions generally combust at about 350°C [44] and 192°C [45], respectively. e weight loss between 500°C and 1200°C is a result of the elimination of hydroxyls adsorbed on the surface.…”
Section: Characterizations Of Zro 2 Nanostructuresmentioning
confidence: 99%