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Dehydra-Decyclization of 2-Methyltetrahydrofuran to Pentadienes on Boron-Containing Zeolites

preprint
submitted on 11.01.2020 and posted on 13.01.2020 by Gaurav Kumar, Dongxia Liu, Dandan Xu, Limin Ren, Michael Tsapatsis, Paul Dauenhauer
Biomass-derived 2-methyltetrahydrofuran (2-MTHF) undergoes tandem ring-opening and dehydration (dehydra-decyclization) to linear pentadienes, namely 1,3-pentadiene and 1,4-pentadiene. It can also fragment to butenes and formaldehyde through a competing retro-Prins condensation pathway. Using detailed kinetic measurements of 2-MTHF dehydra-decyclization on zeolites with disparate acidities (boro- and alumino-silicates) and micropore environments (MFI, MWW, and BEA), weakly acidic borosilicates were shown to exhibit ca. 10-30% higher selectivity to dienes at about five-to-sixty times lower proton-normalized rates than aluminosilicates (453-573 K). Dehydra-decyclization site time yields (STYs) were invariant for aluminosilicates within the investigated frameworks, indicating the absence of pore-confinement influence. However, individual site-normalized reaction rates varied by almost an order of magnitude on borosilicates in the order MWW > MFI > BEA at a given temperature (523 K), indicating the different nature of active sites in these weak solid acids. The diene distribution remained far from equilibrium and was tuned towards the desirable conjugated diene (1,3-pentadiene) by facile isomerization of 1,4-pentadiene. This tuning capability was facilitated by high bed residence times, as well as the smaller micropore sizes among the considered zeolite frameworks. The suppression of competing pathways and promotion of 1,4-pentadiene isomerization events lead to a hitherto unreported ∼86% 1,3-pentadiene yield and an overall ∼ 89% combined linear C5 dienes’ yield at near quantitative (~98%) 2-MTHF conversion on the borosilicate B-MWW, without a significant reduction in diene selectivities for at least 80 hours time-on-stream under low space velocity (0.85 g reactant/g cat./h) and high temperature (658 K) conditions. Finally, starting with iso-conversion levels (ca. 21-26%) and using total turnover numbers (TONs) accrued over the entire catalyst lifetime as the stability criterion, borosilicates were demonstrated to be significantly more stable than aluminosilicates under reaction conditions (~3-6x higher TONs).

Funding

NSF Center for Sustainable Polymers CHE-1413862

Minnesota Corn Growers Association

History

Email Address of Submitting Author

hauer@umn.edu

Institution

University of Minnesota

Country

United States of America

ORCID For Submitting Author

0000-0001-5810-1953

Declaration of Conflict of Interest

No Conflict of Interest

Version Notes

Version 1.0 - Original Submission

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