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Continuous hydrocyclization of aqueous levulinic acid to γ-valerolactone over bi-functional Ru/NbOPO4/SBA-15 catalyst under mild conditions

  • Mariappan Mani
  • , Mariyamuthu Mariyaselvakumar
  • , Ajaikumar Samikannu
  • , Asit Baran Panda
  • , Lakhya Jyoti Konwar*
  • , Jyri Pekka Mikkola
  • *Tämän työn vastaava kirjoittaja

Tutkimustuotos: LehtiartikkeliArtikkeliTieteellinenvertaisarvioitu

14 Sitaatiot (Scopus)

Abstrakti

Herein, we demonstrate that surface acid-base properties have marked effect upon the performance (activity, selectivity and stability) of supported Ru catalysts upon tandem hydrocyclization (hydrogenation-dehydration) of aqueous levulinic acid. A mesoporous bi-functional Ru/NbOPO4/SBA-15 catalyst incorporating highly dispersed Ru sites and well balanced strong Brønsted acidic sites (optimum B/L and M+S/W ratio) was identified, which outperformed the benchmark monofuncational (Ru/SBA-15, Ru/MCM-41) and physically blended bi-functional catalysts (Ru catalysts mixed with acid co-catalysts e.g. NbOPO4/Amberlyst-15). Further, the catalyst also demonstrated remarkable stability in a fixed-bed reactor, maintaining steady activity and γ-valerolactone selectivity (72–86%) during ca. 300 h time on stream (10 bar, 90–100 °C), corroborating its industrial potential. The exceptional performance and durability of the bi-functional catalyst was attributed to the presence of well dispersed hydrothermally and chemically stable acid (NbOPO4) and redox (Ru) sites.

AlkuperäiskieliEnglanti
Artikkeli118744
Sivumäärä16
JulkaisuApplied Catalysis A: General
Vuosikerta643
DOI - pysyväislinkit
TilaJulkaistu - 5 elok. 2022
OKM-julkaisutyyppiA1 Julkaistu artikkeli, soviteltu

Rahoitus

The PRIS registration number of this publication is CSIR-CSMCRI – 04/2022 . Financial support from SERB ( SRG/2020/000325 ) and MLP0028 from CSIR , New Delhi are gratefully acknowledged. The authors also thank the Analytical Division and Centralized Instrumental Facilities of this institute for analytical support. The PRIS registration number of this publication is CSIR-CSMCRI – 04/2022. Financial support from SERB (SRG/2020/000325) and MLP0028 from CSIR, New Delhi are gratefully acknowledged. The authors also thank the Analytical Division and Centralized Instrumental Facilities of this institute for analytical support.

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