Brent H. Shanks

ORCID: 0000-0002-1805-415X
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About
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Research Areas
  • Catalysis for Biomass Conversion
  • Catalysis and Hydrodesulfurization Studies
  • Thermochemical Biomass Conversion Processes
  • Mesoporous Materials and Catalysis
  • Lignin and Wood Chemistry
  • Biofuel production and bioconversion
  • Catalytic Processes in Materials Science
  • Zeolite Catalysis and Synthesis
  • Enzyme Catalysis and Immobilization
  • Catalysts for Methane Reforming
  • Catalysis and Oxidation Reactions
  • Microbial Metabolic Engineering and Bioproduction
  • Chemistry and Chemical Engineering
  • Electrocatalysts for Energy Conversion
  • Biodiesel Production and Applications
  • Carbon dioxide utilization in catalysis
  • Carbon Dioxide Capture Technologies
  • Advanced NMR Techniques and Applications
  • Asymmetric Hydrogenation and Catalysis
  • Industrial Gas Emission Control
  • Nanomaterials for catalytic reactions
  • Chemical Looping and Thermochemical Processes
  • Thermal and Kinetic Analysis
  • Supercapacitor Materials and Fabrication
  • Polyoxometalates: Synthesis and Applications

Iowa State University
2016-2025

Joint BioEnergy Institute
2024

Ames National Laboratory
2002-2021

Bissell (United States)
2017-2021

Environmental Technologies (United States)
2006-2011

Lawrence Technological University
2009

Schlumberger (United States)
2009

California Institute of Technology
1987-1989

General Motors (United States)
1989

Interest in utilizing biorenewable feedstocks to produce fuels and chemicals has risen greatly the past decade due economic, political environmental concerns associated with diminishing petroleum reserves. A fundamental challenge lying ahead development of efficient processes utilize biomass feedstock is that, unlike their counterparts, contains an excess amount oxygen. Therefore, catalytic strategies such as dehydration hydrogenolysis amongst others have been extensively studied platform...

10.1039/c3gc41365a article EN Green Chemistry 2013-11-05

We report the catalytic conversion of glucose in high yields (62%) to 5-hydroxymethylfurfural (HMF), a versatile platform chemical. The reaction system consists Lewis acid metal chloride (e.g., AlCl3) and Brønsted (HCl) biphasic reactor consisting water an alkylphenol compound (2-sec-butylphenol) as organic phase. presence acidity proceeds through tandem pathway involving isomerization fructose, followed by dehydration fructose HMF. phase extracts 97% HMF produced, while both catalysts remain aqueous

10.1021/cs300192z article EN ACS Catalysis 2012-04-18

In the present study, pyrolysis of corn stover lignin was investigated by using a micro-pyrolyzer coupled with GC-MS/FID (FID=flame ionization detector). The system has pyrolysis-vapor residence times 15-20 ms, thus providing regime minimal secondary reactions. primary product distribution obtained from is reported. Over 84 % mass balance and almost complete closure on carbon achieved. another set experiments, vapors emerging are condensed to obtain lignin-derived bio-oil. chemical...

10.1002/cssc.201100133 article EN ChemSusChem 2011-09-21

Abstract Hemicellulose is one of the major constituents biomass. Surprisingly, only very limited information regarding its product distribution under fast pyrolysis conditions available in literature. In present study, a combination several analytical techniques, including micro‐pyrolyzer‐GC‐MS/FID, gas analysis, and capillary electrophoresis, were used to study primary hemicelluloses extracted purified from switchgrass. A total 16 products identified quantified, which accounted for 85 %...

10.1002/cssc.201000425 article EN ChemSusChem 2011-05-05

Previously, the primary product distribution resulting from fast pyrolysis of cellulose, hemicellulose, and lignin was quantified. This study extends analysis to examinations interactions between cellulose–hemicellulose cellulose–lignin, which were determined by comparing products their native mixture, physical superposition individual components. Negligible found for both binary mixtures. For no significant interaction identified either. In case cellulose–lignin herbaceous biomass exhibited...

10.1021/sc500664h article EN ACS Sustainable Chemistry & Engineering 2014-12-23

Removing excess nitrate (NO3–) from waste streams has become a significant environmental and health topic. However, realizing highly selective NO3– conversion toward N2, primarily via electrocatalytic conversions, proven challenging, largely because of the kinetically uncontrollable NO3–-to-NO2– pathway unfavorable N–N coupling. Herein, we discovered unique ultra-high NO3–-to-NO2–activity on oxide-derived silver (OD-Ag). Up to 98% selectivity 95% Faradaic efficiency (FE) NO2– were observed...

10.1021/acscatal.1c01525 article EN ACS Catalysis 2021-06-25

Electrocatalytic hydrogenation and oxidation of 5-(hydroxymethyl)furfural in one paired electrolyzer produces two biorenewable monomers with a combined electron efficiency 187%.

10.1039/c9gc02264c article EN cc-by-nc Green Chemistry 2019-01-01

The use of polar aprotic solvents in acid-catalyzed biomass conversion reactions can lead to improved reaction rates and selectivities. We show that further increases catalyst performance be achieved through the addition inorganic salts, specifically chlorides. Reaction kinetics studies Brønsted dehydration fructose hydroxymethylfurfural (HMF) catalytic concentrations chloride salts leads a 10-fold increase reactivity. Furthermore, increased HMF yields using mixed with Ab initio molecular...

10.1038/s41467-019-09090-4 article EN cc-by Nature Communications 2019-03-08

The chemical industry is currently reliant on a historically inexpensive, petroleum-based carbon feedstock that generates small collection of platform chemicals from which highly efficient conversions lead to the manufacture large variety products. Recently, number factors have coalesced provide impetus explore alternative renewable sources carbon. Here we discuss potential impact shifting non-renewable sources. This change biological will an opportunity for research community contribute...

10.1111/j.1365-313x.2008.03484.x article EN The Plant Journal 2008-05-01

Fast pyrolysis of lignocellulosic biomass, utilizing moderate temperatures ranging from 400 to 600 °C, produces a primary liquid product (pyrolytic bio-oil), which is potentially compatible with existing petroleum-based infrastructure and can be catalytically upgraded fuels chemicals. In this work, experiments were conducted micropyrolyzer coupled gas chromatography–mass spectrometry/flame ionization detector system investigate fast neat cellulose other glucose-based carbohydrates. A...

10.1021/ie502259w article EN publisher-specific-oa Industrial & Engineering Chemistry Research 2014-07-24

Bioprivileged molecules generated from biomass can be converted to both novel and drop-in replacements.

10.1039/c7gc00296c article EN Green Chemistry 2017-01-01

Recent advances in metabolic engineering have allowed for the production of a wide array molecules via biocatalytic routes. The high selectivity biocatalysis to remove functionality from biomass can be used produce platform that are suitable subsequent upgrading over heterogeneous catalysts. Accordingly, more robust continuous processing by chemical catalysis could leveraged upgrade biologically derived direct or functional replacements petroleum products. Herein, we highlight recent results...

10.1021/cs500364y article EN ACS Catalysis 2014-05-15

Abstract Natural oils and fats are emerging as a biobased alternative feedstock to conventional crude oil in the production of chemicals transportation fuel. However, many these not currently cost competitive with petrochemicals because high raw material costs. To improve economic outlook chemicals, use suitable catalysts becomes imperative. Recently, discovery advanced synthesis strategies such supramolecular‐assembled mesoporous materials has created new opportunities tailoring catalyst...

10.1007/s11746-006-1179-x article EN Journal of the American Oil Chemists Society 2006-02-01

The carbonation of CaO is an attractive method for removing CO2 from hot gas mixtures. However, regeneration and reuse a CaO-based sorbent causes gradual decline in absorption capacity, which ultimately limits the life material. Various methods have been proposed increasing cycle performance sorbent. Two these were selected further investigation. One incorporates "inert" material sorbent, while second stabilizes through controlled sintering. Promising results achieved with both when they...

10.1021/ie8007743 article EN Industrial & Engineering Chemistry Research 2008-09-25

Triacetic acid lactone is demonstrated to be a versatile biorenewable molecule with potential as platform chemical for the production of commercially valuable bifunctional intermediates and end products, such sorbic acid.

10.1039/c2gc35343a article EN Green Chemistry 2012-01-01

As biomass pyrolysis is a promising technology for producing renewable fuels, mechanistic descriptions of thermal decomposition are increasing interest. While previous studies have demonstrated that glucose key primary intermediate and elucidated many important elementary mechanisms in its pyrolysis, questions remain. For example, there several proposed evolution an product platform chemical, 5-hydroxymethylfurfural (5-HMF), but evaluation with different methodologies has hindered...

10.1021/sc500113m article EN publisher-specific-oa ACS Sustainable Chemistry & Engineering 2014-04-23
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