首页|Siliceous self-pillared pentasil (SPP) zeolite with incorporated phosphorus groups in catalytic formation of butadiene by dehydra-decyclization of tetrahydrofuran: Study of catalyst stability by NMR and REDOR analysis

Siliceous self-pillared pentasil (SPP) zeolite with incorporated phosphorus groups in catalytic formation of butadiene by dehydra-decyclization of tetrahydrofuran: Study of catalyst stability by NMR and REDOR analysis

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Siliceous self-pillared pentasi l (SPP) zeolite catalysts with incorporated phosphorus groups were synthesized using four different percentages of P, obtaining a network of nanosheets in a house-of-cards arrangement. The catalysts were used in the dehydra-decyclization of tetrahydrofuran (THF) as biomass-derived molecule to obtain 1,3-butadiene. The presence and stability of phosphate (PO43-) and phosphite (PO33-) groups incorporated in the SPP zeolite framework was evidenced. The analysis of fresh and used catalysts by nuclear magnetic resonance (NMR) tests showed that 95% phosphorus in zeolite catalysts is present as orthophosphate groups and less than 5% as pyrophosphate or other polyphosphate groups. The P bonded to Si (Si-O-P, corresponding to orthophos-phate groups), identified by 31 P-{29Si}-Rotational Echo Double Resonance (REDOR)-NM R analysis, are proposed as the active sites responsible for the dehydra-decyclization of T H F to obtain 1,3-butadiene. The P-SPP zeolite catalyst with 0.2 ratio of precursors P and Si in the synthesis, presented the best performance.

P-SPPBiomass-derivedTHFButadieneTetrahydrofuranREDOR N MRETHANOL13-BUTADIENESODIUMPERFORMANCESSELECTIVITYHYDROLYSISCONVERSIONACIDOIL

Ruiz-Zamora, Evelin、de la Rosa, Javier Rivera、Maldonado, Carolina Solis、Lucio-Ortiz, Carlos J.、Del Rio, David A. De Haro、Garza-Navarro, Marco A.、Sandoval-Rangel, Ladislao、Morales-Leal, Francisco J.、Wi, Sungsool

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Univ Autonoma Nuevo Leon

Univ Veracruzana

Escuela Ingn & Ciencias

Inst Mexicano Petr

Florida State Univ

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2022

Applied Catalysis

Applied Catalysis

ISSN:0926-860X
年,卷(期):2022.640
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