IONIC LIQUID BASED ARTIFICIAL CELLULASE TYPE CATALYSTS FOR CELLULOSIC ETHANOL PROCESS

doi:10.4066/2591-7331-C1-002

IONIC LIQUID BASED ARTIFICIAL CELLULASE TYPE CATALYSTS FOR CELLULOSIC ETHANOL PROCESS

7^th International Conference on Green Chemistry & Technology
June 18-20, 2018 | Dublin, Ireland

Ananda S Amarasekara

A&M University, USA

Scientific Tracks Abstracts : J Ind Environ Chem

DOI: 10.4066/2591-7331-C1-002

Abstract:

Efficient hydrolysis of lignocellulosic biomass to fermentable sugars is a challenging step and the primary obstacle for the large scale production of cellulosic ethanol. Ionic liquids are well known for their ability to dissolve cellulose and our interest in the search for efficient catalytic methods for saccharification of polysaccharides has led us to develop-SO3H group functionalized Brönsted acidic ionic liquids (BAILs) as solvents as well as catalysts. Later we found that these sulfuric acid derivatives can be used as catalysts in aqueous phase as well. For example, BAIL 1-(1-propylsulfonic)-3-methylimidazolium chloride aqueous solution was shown to be a better catalyst than H2SO4 of the same [H+] for the degradation of cellulose. This observation is an important lead for the development of a BAIL based cellulase mimic type catalyst for depolymerization of cellulose. In an attempt to develop a recyclable, simple enzyme mimic type catalysts we have studied quantitative structure activity relationships (QSAR) of a series of BAIL catalysts and found that activity with different cation types decreases in the order: imidazolium>pyridinium>triethanol ammonium. Furthermore, we have investigated the effects of selected metal ions on 1-(1-propylsulfonic)-3-methylimidazolium chloride BAIL catalyzed hydrolysis of cellulose in water at 140-170°C. The total reducing sugar (TRS) yields produced during the hydrolysis of cellulose (DP~450) in aq. 1-(1-propylsulfonic)-3-methylimidazolium chloride solution at 140170°C using Cr3+, Mn2+, Fe3+, Co2+ Ni2+, Cu2+, Zn2+, and La3+ chlorides as co-catalysts as well as interactions of catalysts with cellulose are shown in the figure below. These results show that cellulose samples heated with Mn2+, Fe3+, Co2+ as co-catalysts produce significantly higher TRS yields compared to the sample heated without the metal ions. The highest catalytic effect enhancement is observed with Mn2+ and produced TRS yields of 59.1, 78.4, 91.8, and 91.9 % at 140, 150, 160, and 170°C respectively; whereas cellulose hydrolyzed without Mn2+ produced TRS yields of 9.8, 16.5, 28.0, and 28.7% at the same four temperatures. This is a 503, 375, 228, and 220% enhancement in TRS yield due to the addition of Mn2+ as a co-catalyst to BAIL catalyzed cellulose hydrolysis at 140, 150, 160 and 170°C respectively. This paper will present the development of BAIL based artificial cellulase type catalysts, QSAR studies, catalyst immobilizations, applications on lignocellulosic biomass materials (corn stover, switchgrass, poplar) and recycling studies.

Biography:

Ananda S Amarasekara is a professor of chemistry at A&M University in Texas, where he has been a faculty member since 2003. He received his PhD. in organic chemistry from City University of New York. The current research interest of his group is to develop acidic ionic liquid based chemocatalytic methods for the processing of biomass to renewable fuels and feedstock chemicals. He is the author of the book “Handbook of Cellulosic Ethanol” and has published more than 100 peer reviewed research articles.

Email:asamarasekara@pvamu.edu

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