2021
DOI: 10.1016/j.fuel.2021.121545
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Hydrodeoxygenation of aliphatic acid over NiFe intermetallic compounds: Insights into the mechanism via model compound study

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Cited by 14 publications
(24 citation statements)
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“…Lauric acid was totally converted to alkanes through lauryl alcohol in 100 min with reduced Ni 3 Fe 1 /SiO 2 (NiFe AC) catalyst as shown in Figure S5. 36 However, with the effect of reaction time shown in Figure 6c, the selectivity to alkanes was only about 10% in 100 min, which indicated that the oxidation process of the Ni 3 Fe 1 /SiO 2 catalyst inhibited the deoxygenation of lauryl alcohol obviously. As the formation of undecane by decarbonylation was the main pathway to produce alkane, the inhibition effect mainly acted on this step.…”
Section: ■ Results and Discussionmentioning
confidence: 94%
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“…Lauric acid was totally converted to alkanes through lauryl alcohol in 100 min with reduced Ni 3 Fe 1 /SiO 2 (NiFe AC) catalyst as shown in Figure S5. 36 However, with the effect of reaction time shown in Figure 6c, the selectivity to alkanes was only about 10% in 100 min, which indicated that the oxidation process of the Ni 3 Fe 1 /SiO 2 catalyst inhibited the deoxygenation of lauryl alcohol obviously. As the formation of undecane by decarbonylation was the main pathway to produce alkane, the inhibition effect mainly acted on this step.…”
Section: ■ Results and Discussionmentioning
confidence: 94%
“…Undecane and dodecane were the products of the decarbonylation and hydrodehydration of lauryl alcohol, respectively. Lauric acid was totally converted to alkanes through lauryl alcohol in 100 min with reduced Ni 3 Fe 1 /SiO 2 (NiFe AC) catalyst as shown in Figure S5 . However, with the effect of reaction time shown in Figure c, the selectivity to alkanes was only about 10% in 100 min, which indicated that the oxidation process of the Ni 3 Fe 1 /SiO 2 catalyst inhibited the deoxygenation of lauryl alcohol obviously.…”
Section: Resultsmentioning
confidence: 99%
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