2017
DOI: 10.1039/c7gc01178d
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Metal-exchanged magnetic β-zeolites: valorization of lignocellulosic biomass-derived compounds to platform chemicals

Abstract: An array of Pd, Fe and Ir exchanged β-zeolites were synthesized, fully characterized, and their catalytic activity evaluated in converting bio-derived compounds to value-added platform chemicals.

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Cited by 37 publications
(33 citation statements)
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“…The data demonstrates that all of the zeolites attain significant (up to almost 8 wt.%) amounts of carbon during the reaction. 79 These results reinforce the notion that carbon is deposited inside the catalyst pores in the form of fine, amorphous particles. Similar effect was reported in literature for methane dry reforming on Ni-Co/Al 2 O 3 -ZrO 2 catalysts.…”
Section: Carbon Deposition On Pure Zeolitessupporting
confidence: 75%
“…The data demonstrates that all of the zeolites attain significant (up to almost 8 wt.%) amounts of carbon during the reaction. 79 These results reinforce the notion that carbon is deposited inside the catalyst pores in the form of fine, amorphous particles. Similar effect was reported in literature for methane dry reforming on Ni-Co/Al 2 O 3 -ZrO 2 catalysts.…”
Section: Carbon Deposition On Pure Zeolitessupporting
confidence: 75%
“…In the absence of catalyst the only product is 2-(diisopropoxymethyl)furan (DPMF) with a yield of 10 %, which is formed by the acetalization of F with two molecules of 2-propanol. [25,26] This product is also observed over the commercial Al 2 O 3 (DPMF = 5 %), together with a minor amount of FA (7 %). The ability of Al 2 O 3 to catalyse the CTH of F has been recently reported although a large catalyst amount was required to work efficiently.…”
Section: Furfural Conversion Over Hydrotalcite-derived Catalystsmentioning
confidence: 65%
“…Contrary to the other two prepared catalysts that present DPMF yields of 2 and 5 %, the Co 3 O 4 −Al 2 O 3 sample did not catalyse the acetalization of F with 2‐propanol. The only side‐product over the Co 3 O 4 −Al 2 O 3 was 2‐(isopropoxymethyl)furan (PMF) with a negligible yield of 1 %, which is formed by the etherification of FA with 2‐propanol (Figure ) . This result implies an outstanding selectivity of 97 % for FA production.…”
Section: Resultsmentioning
confidence: 99%
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