Pyoungchung Kim

Hydrogen production from switchgrass via an integrated pyrolysis–microbial electrolysis process

A new approach to hydrogen production using an integrated pyrolysis-microbial electrolysis process is described. The aqueous stream generated during pyrolysis of switchgrass was used as a substrate for hydrogen production in a microbial electrolysis cell, achieving a maximum hydrogen production rate of 4.3 L H2/L anode-day at a loading of 10 g COD/L-anode-day. Hydrogen yields ranged from 50±3.2% to 76±0.5% while anode Coulombic efficiency ranged from 54±6.5% to 96±0.21%, respectively. Significant conversion of furfural, organic acids and phenolic molecules was observed under both batch and continuous conditions. The electrical and overall energy efficiency ranged from 149-175% and 48-63%, respectively. The results demonstrate the potential of the pyrolysis-microbial electrolysis process as a sustainable and efficient route for production of renewable hydrogen with significant implications for hydrocarbon production from biomass.

Application of water-activated carbon isotherm models to water adsorption isotherms of single-walled carbon nanotubes.

The objective of this study is to understand the interactions of water with novel nanocarbons by implementing semiempirical models that were developed to interpret adsorption isotherms of water in common carbonaceous adsorbents. Water adsorption isotherms were gravimetrically determined on several single-walled carbon nanotube (SWNT) and activated carbon samples. Each isotherm was fitted to the Dubinin-Serpinsky (DS) equation, the Dubinin-Astakov equation, the cooperative multimolecular sorption theory, and the Do and Do equations. The applicability of these models was evaluated by high correlation coefficients and the significance of fitting parameters, especially those that delineate the concentration of hydrophilic functional groups, micropore volume, and the size of water clusters. Samples were also characterized by spectroscopic and adsorption techniques, and properties complementary to those quantified by the fitting parameters were extracted from the data collected. The comparison of fitting parameters with sample characterization results was used as the methodology for selecting the most informative and the best-fitting model. We conclude that the Do equation, as modified by Marban et al., is the most suitable semiempirical equation for predicting from experimental isotherms alone the size of molecular clusters that facilitate adsorption in SWNTs, deconvoluting the experimental isotherms into two subisotherms: adsorption onto hydrophilic groups and filling of micropores, and quantifying the concentration of hydrophilic functional groups, as well as determining the micropore volume explored by water. With the exception of the DS equation, the application of other water isotherm models to SWNTs is not computationally tractable. The findings from this research should aid studies of water adsorption in SWNTs by molecular simulation, which remains the most popular tool for understanding the microscopic behavior of water in nanocarbons.

Regioselective competitive adsorption of water and organic vapor mixtures on pristine single-walled carbon nanotube bundles.

Sequential adsorption of water and organic vapor mixtures onto single-walled carbon nanotube (SWNT) bundles is studied experimentally and by grand canonical Monte Carlo (GCMC) simulation to elucidate the distinct interactions between select adsorbates and the nanoporous structure of SWNTs. Experimental adsorption isotherms on SWNT bundles for hexane, methyl ethyl ketone, cyclohexane, and toluene individually mixed in carrier gases that were nearly saturated with water vapor are compared with the GCMC-simulated isotherms for hexane, as a representative organic, on the external surface of the heterogeneous SWNT bundles. From the nearly perfect overlap between the experimental and simulated isotherms, it is concluded that until near saturation only the internal pore volume of pristine SWNT bundles fills with water. The adsorption of water vapor on the peripheral surface of the bundles remains insignificant, if not negligible, in comparison to the adsorption of water in the internal volume of the bundles. This is in contrast with the adsorption of pure hexane, which exhibits appreciable adsorption both inside the bundles and on their external surface. It is also suggested that during competitive adsorption, water molecules take precedence over small nonpolar and polar organic molecules for adsorption inside SWNTs and leave unoccupied the hydrophobic external surface of the bundles for other more compatible adsorbates.

Effect of pH on surface characteristics of switchgrass-derived biochars produced by fast pyrolysis.

Surface properties of switchgrass-derived biochars produced at fast pyrolysis temperatures of 450, 600 and 800 °C were characterized at different solution pHs in order to determine the structural and chemical changes of artificially-weathered biochars when incorporated into soil. As biochars were acidified from pH 7 to 3, crystalline minerals dissolved slowly releasing nutrients; however, residual minerals were still detected in biochars produced at higher pyrolysis temperatures after pH treatment. Moreover, the amount of exchangeable bases and other inorganic compounds released from the biochars increased when pH decreased. As minerals dissolved from the biochars, total surface area and pore volume were found to increase. Surface functional groups and water vapor adsorption capacity at 0.8 P/Po also increased, whereas the potential CEC of biochars decreased due to the replacement of exchangeable sites by hydrogen ion. Therefore, during the aging process, it is predicted that soil-incorporated biochars will slowly release nutrients with changes in surface functionality and porosity, which are expected to enhance water holding capacity of soil and provide a beneficial habitat for microbial colonization.

Aging of Nanocarbons in Ambient Conditions: probable metastability of carbon nanotubes

We studied the physicochemical properties of several commercially available single- and multi-walled carbon nanotubes (SWNTs and MWNTs) and fullerenes stored in normal ambient conditions for 24 months. We found that SWNTs exhibit a trend of decreasing surface area and pore volume up to 7-15 months but then stabilized, no longer being impacted by sample age or outgassing temperatures. Using X-ray Photoelectron Spectroscopy, we also observed a trend of decreasing surface oxygen in all samples from the beginning with much lower % oxygen observed after 12-15 months of aging under ambient conditions. The surface oxygen then stabilized for the duration of this study. There was also evidence that the total structural-defect concentration, estimated from Raman spectroscopy, was somehow lowered during the aging process. The decrease in surface oxygen is an unexpected phenomenon because most other carbons, such as activated carbons or carbon molecular sieves, either oxidize or remain unaffected by age. We believe that nanocarbons are meta-stable materials (in pseudo-thermodynamic equilibrium), and that their aging in ambient conditions makes them more thermodynamically stable with fixed properties. This new information about the properties of nanocarbons should be further explored as it can help resolve some of the conflicting reports such as those about the environmental impacts of nanomaterials.

Effects of organosolv fractionation time on thermal and chemical properties of lignins

Organosolv fractionation is a promising pathway to separate cellulosic biomass into high purity cellulose, hemicelluloses, and lignin. This work specifically investigates the properties of lignins isolated at specific time points as fractionation progressed, with the intent of correlating fractionation time with lignin purity, yield, thermal and chemical properties. Yellow poplar (Liriodendron tulipifera) was fractionated using a mixture of methyl isobutyl ketone, ethanol, and water with sulfuric acid as catalyst at 140 °C over a two-hour period. Aliquots of the liquor were collected by sampling every 15 min during the fractionation to generate a series of lignins. The results showed that with increased fractionation time, lignin purity improved from 90.3 to 94.6% and the glass transition temperature increased from 117 to 137 °C. The loss of aliphatic OH and increase of phenolic OH with fractionation time led to an increase in condensed structures and increased polydispersity at times greater than 90 min. Principal component analysis of Fourier transform infrared spectroscopic data confirmed the shift to higher purity and more condensed chemical structures with increasing fractionation time. Overall, this study demonstrates that thermal and chemical properties of lignin change with the organosolv fractionation time.

Effect of non-structural organics and inorganics constituents of switchgrass during pyrolysis

Nonstructural components, such as inorganics and organic extractives, present in switchgrass were extracted using water and ethanol, and the resulting nonstructural components-free materials were pyrolyzed to investigate the effect of the inorganic species on the pyrolytic products. The extraction was performed for switchgrass materials harvested from three consecutive growing seasons, removing 8.5 wt% of the organic extractives in the first season biomass, and 5.8 and 6.3 wt% in the second and third season, respectively, on total dry basis of biomass. In addition to organic extractives, 0.7 to 2.7 wt% of ash were extracted. Specifically, 99 % and 59 % of total K and Mg were removed from the switchgrass harvested in the second and third growing season. Thermogravimetric analysis demonstrated that a predominant reduction of K and Mg content in the biomass increased temperature at which mass loss rate is maximized in the decomposition of cellulose, hemicellulose, and lignin. The reduction of K and Mg content also affected pyrolytic products generated at 450 oC. The chromatographic peak area percentage of levoglucosan from the extracted samples in the second and third growing season was two to three times higher than that from the extracted samples in the first growing season, showing a strong negative correlation with K and Mg content, whereas most of the light oxygenated and furanic/pyranic/cyclopentanic products exhibited a strong positive correlation with K and Mg content. We concluded that the removal of nonstructural components prior to thermochemical conversion processes such pyrolysis can potentially produce a valuable extractives stream while removing catalytic inorganics that negatively impact downstream pyrolysis process.