Pushing the Limits on Metal-Organic Frameworks as a Catalyst Support

NU-1000 Supported Tungsten Catalysts for o-Xylene Isomerization and Disproportionation

Sol Ahn, Scott L. Nauert, Cassandra T. Buru, Martino Rimoldi, Hyeju Choi, Neil M. Schweitzer, Joseph T Hupp, Omar K. Farha, Justin M Notestein

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

Acid-catalyzed skeletal C-C bond isomerizations are important benchmark reactions for the petrochemical industries. Among those, o-xylene isomerization/disproportionation is a probe reaction for strong Brønsted acid catalysis, and it is also sensitive to the local acid site density and pore topology. Here, we report on the use of phosphotungstic acid (PTA) encapsulated within NU-1000, a Zr-based metal-organic framework (MOF), as a catalyst for o-xylene isomerization at 523 K. Extended X-ray absorption fine structure (EXAFS), 31P NMR, N2 physisorption, and X-ray diffraction (XRD) show that the catalyst is structurally stable with time-on-stream and that WOx clusters are necessary for detectable rates, consistent with conventional catalysts for the reaction. PTA and framework stability under these aggressive conditions requires maximal loading of PTA within the NU-1000 framework; materials with lower PTA loading lost structural integrity under the reaction conditions. Initial reaction rates over the NU-1000-supported catalyst were comparable to a control WOx-ZrO2, but the NU-1000 composite material was unusually active toward the transmethylation pathway that requires two adjacent active sites in a confined pore, as created when PTA is confined in NU-1000. This work shows the promise of metal-organic framework topologies in giving access to unique reactivity, even for aggressive reactions such as hydrocarbon isomerization.

Original languageEnglish
Pages (from-to)8535-8543
Number of pages9
JournalJournal of the American Chemical Society
Volume140
Issue number27
DOIs
Publication statusPublished - Jul 11 2018

Fingerprint

Phosphotungstic Acid
Tungsten
Xylene
Isomerization
Catalyst supports
Metals
Catalysts
Acids
Topology
Benchmarking
Physisorption
X ray absorption
Structural integrity
Hydrocarbons
Catalysis
Petrochemicals
X-Ray Diffraction
Reaction rates
Catalytic Domain
Industry

ASJC Scopus subject areas

  • Catalysis
  • Chemistry(all)
  • Biochemistry
  • Colloid and Surface Chemistry

Cite this

Pushing the Limits on Metal-Organic Frameworks as a Catalyst Support : NU-1000 Supported Tungsten Catalysts for o-Xylene Isomerization and Disproportionation. / Ahn, Sol; Nauert, Scott L.; Buru, Cassandra T.; Rimoldi, Martino; Choi, Hyeju; Schweitzer, Neil M.; Hupp, Joseph T; Farha, Omar K.; Notestein, Justin M.

In: Journal of the American Chemical Society, Vol. 140, No. 27, 11.07.2018, p. 8535-8543.

Research output: Contribution to journalArticle

Ahn, Sol ; Nauert, Scott L. ; Buru, Cassandra T. ; Rimoldi, Martino ; Choi, Hyeju ; Schweitzer, Neil M. ; Hupp, Joseph T ; Farha, Omar K. ; Notestein, Justin M. / Pushing the Limits on Metal-Organic Frameworks as a Catalyst Support : NU-1000 Supported Tungsten Catalysts for o-Xylene Isomerization and Disproportionation. In: Journal of the American Chemical Society. 2018 ; Vol. 140, No. 27. pp. 8535-8543.
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