Selective conversion of bio-derived ethanol to renewable BTX over Ga-ZSM-5

Zhenglong Li, Andrew W. Lepore, Mariam F. Salazar, Guo Shiou Foo, Brian H. Davison, Zili Wu, Chaitanya K. Narula

Research output: Contribution to journalArticlepeer-review

62 Scopus citations

Abstract

Selective conversion of bio-derived ethanol to benzene, toluene and xylenes (BTX) is desirable for producing renewable BTX. In this work, we show that addition of Ga to H-ZSM-5 leads to a two-fold increase in the BTX yield as compared with H-ZSM-5 when ethanol is converted over these zeolites at 450 °C and ambient pressure. Besides promoting BTX formation, Ga also plays an important role in enhancing molecular hydrogen production and suppressing hydrogen transfer reactions for light alkane formation. The ion exchange synthesis of Ga-ZSM-5 results in the majority of Ga at the outer surface of zeolite crystals as extra-zeolitic Ga2O3 particles and only a small fraction of Ga exchanging with the Brønsted acid sites which appears to be responsible for higher ethanol conversion to BTX. The interface between H-ZSM-5 and Ga2O3 particles is not active since H-ZSM-5 and the physical mixture of β-Ga2O3/H-ZSM-5 furnish an almost identical product distribution. Hydrogen reduction of the physical mixtures facilitates movement of Ga to ion exchange locations and dramatically increases the BTX yield becoming comparable to those obtained over ion-exchanged Ga-ZSM-5, suggesting that exchanged Ga(iii) cations are responsible for the increased BTX production. A linear correlation between the BTX site time yield and exchanged Ga sites further confirms that Ga occupying cationic sites are active sites for enhancing BTX formation. Reduction of physical mixtures (β-Ga2O3/H-ZSM-5) also provides an economical and environmentally friendly non-aqueous method for large scale catalyst synthesis without sacrificing catalyst performance for ethanol conversion application.

Original languageEnglish
Pages (from-to)4344-4352
Number of pages9
JournalGreen Chemistry
Volume19
Issue number18
DOIs
StatePublished - 2017

Funding

This research is sponsored by the BioEnergy Technologies Office, Office of Energy Efficiency and Renewable Energy, U.S. Department of Energy, under contract DE-AC05-00OR22725 with UT-Battelle, LLC. GSF and ZW are supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Chemical Sciences, Geosciences, and Biosciences Division. The n-propylamine TPD work was conducted at the Center for Nanophase Materials Sciences, which is a DOE Office of Science User Facility. The assistance of Dr Ercan Cakmak and Dr Harry Meyer for XRD and XPS analysis respectively is greatly acknowledged. We also thank Dr Todd Toops and Dr Andrew Binder for assisting with the NH3-TPD experiments. This manuscript has been authored by UT-Battelle, LLC under Contract No. DE-AC05-00OR22725 with the U.S. Department of Energy. The United States Government retains and the publisher, by accepting the article for publication, acknowledges that the United States Government retains a non-exclusive, paid-up, irrevocable, world-wide license to publish or reproduce the published form of this manuscript, or allow others to do so, for United States Government purposes. The Department of Energy will provide public access to these results of federally sponsored research in accordance with the DOE Public Access Plan (http://energy.gov/downloads/ doe-public-access-plan).

FundersFunder number
U.S. Department of EnergyDE-AC05-00OR22725
Office of Science
Office of Energy Efficiency and Renewable Energy
Basic Energy Sciences
Bioenergy Technologies Office
Chemical Sciences, Geosciences, and Biosciences Division

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