Interaction of oxalate with ß-glucan: Implications for the fungal extracellular matrix, and metabolite transport.

ß-glucan is the major component of the extracellular matrix (ECM) of many fungi, including wood degrading fungi. Many of these species also secrete oxalate into the ECM. Our research demonstrates that ß-glucan forms a novel, previously unreported, hydrogel at room temperature with oxalate. Oxalate was found to alter the rheometric properties of the ß-glucan hydrogels, and modeling showed that ß-glucan hydrogen bonds with oxalate in a non-covalent matrix. Change of oxalate concentration also impacted the diffusion of a high-molecular-weight protein through the gels. This finding has relevance to the diffusion of extracellular enzymes into substrates and helps to explain why some types of wood-decay fungi rely on non-enzymatic degradation schemes for carbon cycling. Further, this research has potential impact on the diffusion of metabolites in association with pathogenic/biomedical fungi.

Hydroxyapatite catalyzed hydrothermal liquefaction transforms food waste from an environmental liability to renewable fuel.

Food waste is an abundant and inexpensive resource for the production of renewable fuels. Biocrude yields obtained from hydrothermal liquefaction (HTL) of food waste can be boosted using hydroxyapatite (HAP) as an inexpensive and abundant catalyst. Combining HAP with an inexpensive homogeneous base increased biocrude yield from 14 ± 1 to 37 ± 3%, resulting in the recovery of 49 ± 2% of the energy contained in the food waste feed. Detailed product analysis revealed the importance of fatty-acid oligomerization during biocrude formation, highlighting the role of acid-base catalysts in promoting condensation reactions. Economic and environmental analysis found that the new technology has the potential to reduce US greenhouse gas emissions by 2.6% while producing renewable diesel with a minimum fuel selling price of $1.06/GGE. HAP can play a role in transforming food waste from a liability to a renewable fuel.

Rational design of solid-acid catalysts for cellulose hydrolysis using colloidal theory.

Solid-acid catalysts functionalized with catalytic groups have attracted intense interest for converting cellulose into soluble products. However, design of solid-7 acid catalysts has been guided by molecular level interactions and the actual mechanism of cellulose-solid-acid catalyst particles adsorption remains unknown. Here, colloidal stability theory, DLVO, is used to rationalize the design of solid acids for targeted cellulose adsorption. In nearly all cases, an energy barrier, arising from electrostatic repulsion and much larger than the energy associated with thermal fluctuations, prevents close contact between the solid acid and cellulose. Polymer-based solid-acid substrates such as polystyrene and Nafion are especially ineffective as their interaction with cellulose is dominated by the repulsive electrostatic force. Carbon and metal oxides have potential to be effective for cellulose-solid-acid interaction as their attractive van der Waals interaction can offset the repulsive electrostatic interaction. The effects of reactor temperature and shear force were evaluated, with the finding that reactor temperature can minimize the catalyst-cellulose interaction barrier, promoting coagulation, but that the shear force in a typical laboratory reactor cannot. We have evaluated strategies for enhancing cellulose-catalyst interaction and conclude that raising reaction temperature or synthesizing acid/base bifunctional catalysts can effectively diminish electrostatic repulsion and promote cellulose-catalyst coagulation. The analysis presented here establishes a rational method for designing solid acid catalysts for cellulose hydrolysis.

Critical Role of Tricyclic Bridges Including Neighboring Rings for Understanding Raman Spectra of Zeolites.

Raman spectroscopy of network solids such as zeolites is critical for shedding light on collective vibrations of medium-range structures such as rings that exist in crystals and that form during crystallization processes. Despite this importance, assignments of Raman spectra are not completely understood, though it is often assumed that Raman bands can be assigned to individual rings. We report a systematic zeolite synthesis, spectroscopy, and periodic DFT study of several all-silica zeolites to test this assumption and to determine the fundamental structural motifs that explain Raman spectral features. We have discovered from normal-mode analysis that Raman bands can be assigned to tricyclic bridges-three zeolite rings that share a common Si-O-Si bridge. Furthermore, we have found that the vibrational frequency of a given Raman band can be correlated to the smallest ring of its tricyclic bridge and not to the ring that is actually vibrating. Finally, we have discovered a precise anticorrelation between Raman frequency and Si-O-Si angle. These discoveries open new ways to investigate structures of network materials made of corner-sharing tetrahedra and to study crystallization from amorphous gels where structural information is limited.

ZSM-5 decrystallization and dealumination in hot liquid water.

Zeolites have recently attracted attention for upgrading renewable resources in the presence of liquid water phases; however, the stability of zeolites in the presence of liquid-phase water is not completely understood. Accordingly, the stability of the ZSM-5 framework and its acid sites was studied in the presence of water at temperatures ranging from 250 to 450 °C and at pressures sufficient to maintain a liquid or liquid-like state (25 MPa). Treated samples were analyzed for framework degradation and Al content and coordination using a variety of complementary techniques, including X-ray diffraction, electron microscopy, N2 sorption, 27Al and 29Si NMR spectroscopy, and several different types of infrared spectroscopy. These analyses indicate that the ZSM-5 framework retains >80% crystallinity at all conditions, and that 300-400 °C are the most aggressive. Decrystallization appears to initiate primarily at crystal surfaces and share many characteristics in common with alkali promoted desilication. Liquid water treatment promotes ZSM-5 dealumination, following a mechanism analogous to that observed under steaming conditions: initiation by Al-O hydrolysis, Al migration to the surface, and finally deposition as extra framework Al or possibly complete dissolution under some conditions. As with the framework, dealumination is most aggressive at 300-400 °C. Several models were evaluated to capture the non-Arrhenius effect of temperature on decrystallization and dealumination, the most successful of which included temperature dependent values of the water auto-ionization constant. These results can help interpretation of previous studies on ZSM-5 catalysis in hot liquid water and suggest future approaches to extend catalyst lifetime.

Engineered microbial biofuel production and recovery under supercritical carbon dioxide.

Culture contamination, end-product toxicity, and energy efficient product recovery are long-standing bioprocess challenges. To solve these problems, we propose a high-pressure fermentation strategy, coupled with in situ extraction using the abundant and renewable solvent supercritical carbon dioxide (scCO2), which is also known for its broad microbial lethality. Towards this goal, we report the domestication and engineering of a scCO2-tolerant strain of Bacillus megaterium, previously isolated from formation waters from the McElmo Dome CO2 field, to produce branched alcohols that have potential use as biofuels. After establishing induced-expression under scCO2, isobutanol production from 2-ketoisovalerate is observed with greater than 40% yield with co-produced isopentanol. Finally, we present a process model to compare the energy required for our process to other in situ extraction methods, such as gas stripping, finding scCO2 extraction to be potentially competitive, if not superior.

Electrocatalytic reduction of acetone in a proton-exchange-membrane reactor: a model reaction for the electrocatalytic reduction of biomass.

Acetone was electrocatalytically reduced to isopropanol in a proton-exchange-membrane (PEM) reactor on an unsupported platinum cathode. Protons needed for the reduction were produced on the unsupported Pt-Ru anode from either hydrogen gas or electrolysis of water. The current efficiency (the ratio of current contributing to the desired chemical reaction to the overall current) and reaction rate for acetone conversion increased with increasing temperature or applied voltage for the electrocatalytic acetone/water system. The reaction rate and current efficiency went through a maximum with respect to acetone concentration. The reaction rate for acetone conversion increased with increasing temperature for the electrocatalytic acetone/hydrogen system. Increasing the applied voltage for the electrocatalytic acetone/hydrogen system decreased the current efficiency due to production of hydrogen gas. Results from this study demonstrate the commercial feasibility of using PEM reactors to electrocatalytically reduce biomass-derived oxygenates into renewable fuels and chemicals.

Searching for microporous, strongly basic catalysts: experimental and calculated 29Si NMR spectra of heavily nitrogen-doped Y zeolites.

Nitrogen substituted zeolites with high crystallinity and microporosity are obtained by nitrogen substitution for oxygen in zeolite Y. The substitution reaction is performed under ammonia flow by varying the temperature and reaction time. We examine the effect of aluminum content and charge-compensating cation (H(+)/Na(+)/NH(4)(+)) on the degree of nitrogen substitution and on the preference for substitution of Si-O-Al vs Si-O-Si linkages in the FAU zeolite structure. Silicon-29 magic angle spinning (MAS) nuclear magnetic resonance (NMR) and (1)H/(29)Si cross-polarization MAS NMR spectroscopy have been used to probe the different local environments of the nitrogen-substituted zeolites. Experimental data are compared to simulated NMR spectra obtained by constructing a compendium (>100) of zeolite clusters with and without nitrogen, and by performing quantum calculations of chemical shifts for the NMR-active nuclei in each cluster. The simulated NMR spectra, which assume peak intensities predicted by statistical analysis, agree remarkably well with the experimental data. The results show that high levels of nitrogen substitution can be achieved while maintaining porosity, particularly for NaY and low-aluminum HY materials, without significant loss in crystallinity. Experiments performed at lower temperatures (750-800 degrees C) show a preference for substitution at Si-OH-Al sites. No preference is seen for reactions performed at higher temperatures and longer reaction times (e.g., 850 degrees C and 48 h).

Microwave synthesis of zeolites: effect of power delivery.

The effect of microwave power magnitude and pulsing frequency on the synthesis enhancement of zeolites, silicoaluminophosphate SAPO-11, silicalite, and NaY, was studied. Pulsing the microwave power compared to continuous delivery at the same averaged fed microwave power showed no effect on the nucleation and crystallization rates of SAPO-11, silicalite, or NaY. However, SAPO-11 synthesized with continuous microwave power delivery produced larger particles compared to pulsed microwave power with the same reaction time (3.77 microm for continuous versus 2.49 microm for pulsed 1 s on; 3 s off). Further, pulsed microwave power delivery used lower steady state power to maintain the same reaction temperature compared to continuous power delivery (55 W compared to 65 W, respectively). The microwave power used to heat the reaction precursors of SAPO-11 and silicalite was varied by applying cooling gas at various rates while maintaining the reaction temperatures. Significant enhancement of the crystallization rate for SAPO-11 was observed with increasing the fed microwave power (0.014 min(-1) at 65 W, 0.030 min(-1) at 130 W, and 0.066 min(-1) at 210 W), with little effect on the nucleation time. The crystallization rate to microwave power relation was found to obey a power curve (y = 0.4259x(2) - 0.2776x + 0.8517). Lower microwave power produced larger crystals but required longer reaction time to complete crystallization (3.77 microm at 65 W compared to 2.04 microm at 210 W). Conversely, silicalite synthesis at 150 degrees C was found to be independent of the magnitude of the applied microwave power.

Microwave synthesis of SAPO-11 and AlPO-11: aspects of reactor engineering.

AlPO-11 and SAPO-11 are synthesized using microwave heating. The effects of precursor volume, reaction temperature, reactor geometry, stirring, applicator type and frequency on the microwave synthesis of SAPO-11 and AlPO-11 are studied. The nucleation time and crystallization rate are determined from crystallization curves for SAPO-11 (and/or AlPO-11), for the various parameters investigated. Increasing volume of the reacting material decreases the reaction rate of SAPO-11 at 160 degrees C. In particular, the nucleation time increases with increase in the reaction volume. Increasing the reaction temperature increases the crystallization rate and decreases the nucleation time, however it decreases the particle size. Nucleation of SAPO-11 and AlPO-11 under microwave heating is strongly dependant on the reaction temperature. Using wider geometry vessel (33 mm compared to 11 mm diameter) enhances the reaction rate, producing larger crystals in the same reaction time, even though the crystallization rate is decreased. The crystallization rate is enhanced by applicator type in the following order CEM MARS-5 oven>CEM Discover "focused" system>monomode waveguide. Stirring the reacting solution during heating affects primarily the nucleation time. The effect of microwave frequency on the nucleation and growth of SAPO-11 shows a dependence on the applicator type more than the specific frequency, for the frequency range 2.45-10.5 GHz. The difference between the crystallization rate observed at higher frequencies and that at 2.45 GHz maybe due to the multimode nature of the waveguide at frequencies above 2.45 GHz. Sweeping the microwave frequency linearly between 8.7 and 10.5 GHz at rates of 10 min(-1) and 100 min(-1) shows an intermediate crystallization curve to that for fixed frequencies of 2.45 GHz and that for 5.8, 8.7 and 10.5 GHz.

Spectroscopic signatures of nitrogen-substituted zeolites.

Nanoporous acid catalysts such as zeolites form the backbone of catalytic technologies for refining petroleum. With the promise of a biomass economy, new catalyst systems will have to be discovered, making shape-selective base catalysts especially important because of the high oxygen content in biomass-derived feedstocks. Strongly basic zeolites are attractive candidates, but such materials are notoriously difficult to make due to the strong inherent acidity of aluminosilicates. Several research groups have endeavored to produce strongly basic zeolites by treating zeolites with amines, but to date there is no compelling evidence that nitrogen is incorporated into zeolite frameworks. In this communication, we detail synthesis, NMR spectroscopy, and quantum mechanical calculations showing that nitrogen adds onto both surface and interior sites while preserving the framework structure of zeolites. This finding is crucial for the rational design of new biomass-refinement catalysts, allowing 50 years of zeolite science to be brought to bear on the catalytic synthesis of biofuels.

How could and do microwaves influence chemistry at interfaces?

Many chemical reactions may be accelerated by order(s) of magnitude when exposed to microwaves. Reaction selectivities are often enhanced. Reasons for microwave reaction enhancements are speculative, often conflicting. We have demonstrated that microwaves can change the energies and/or the "effective temperature" of individual species at interfaces. Changes in the relative energies of reacting species or intermediates are shown by Monte Carlo simulation to lead to the observed enhancements in reaction rates or selectivities. Moreover, variations in microwave exposure in time or space can result in significant rate enhancement. Such variations may provide unique rate control.

Microwave synthesis of zeolites. 2. Effect of vessel size, precursor volume, and irradiation method.

The enhancement of synthesis reactions under microwave heating is dependent on many complex factors. We investigated the importance of several reaction engineering parameters relevant to microwave synthesis. Of interest to this investigation were the reaction vessel size, volume of precursor reacted, microwave power delivery, and microwave cavity design. The syntheses of NaY zeolite and beta-zeolite were carried out under a number of varying conditions to determine the influence of these parameters on the nucleation rate, the crystallization rate, and the particle size and morphology. The rates of NaY and beta-zeolite nucleation and crystallization were more rapid in the multimode CEM MARS-5 oven compared to the more uniform field CEM Discover. The faster synthesis rate in the MARS-5 may be the result of the multimode microwave electric field distribution. Slower rates of NaY and beta-zeolite formation observed in the Discover and a circular waveguide may be the result of a more uniform microwave electric field distribution. Changes in reaction vessel size and precursor volume during the microwave synthesis of beta- and NaY zeolite were found to influence the rate of zeolite formation. These results indicate that reactor geometry needs to be considered in the design of systems used for microwave synthesis. Comparative synthesis reactions were carried out with conventional heating, and microwave heating was shown to be up to over an order of magnitude faster for most of these syntheses.

Physical adsorption analysis of intact supported MFI zeolite membranes.

We compare the adsorption properties of intact supported silicalite membranes with those of silicalite powder and of alumina supports using nitrogen and argon as adsorbates at 77 K. We disentangle contributions from the membrane and support and find that the support contributes significantly to the total quantity adsorbed due to its relative thickness. The micropore-filling regions of the adsorption isotherms of the powder and the supported membrane are nearly identical for the membranes studied, but the isotherms differ at higher pressures--the supported membranes exhibit a much higher quantity adsorbed than the powders. Despite this difference, no hysteresis is observed in the membrane isotherms, indicating a lack of mesoporosity (pores in the 2-50 nm range) in either membrane or support for this preparation. We estimate argon transport fluxes at steady state by assuming surface diffusion with both a constant and concentration-dependent Maxwell-Stefan diffusion coefficient in the zeolite and the support. Further, we use the respective adsorption isotherms to determine the thermodynamic correction factors--that is, the ratios of the Fick and Maxwell-Stefan diffusion coefficients--required to solve the diffusion equation. The estimated argon flux is virtually the same using adsorption data from powders and membranes. For the relatively thick supports used in our study (approximately 2 mm), we find that the support exerts a much greater influence on the predicted fluxes for a wide range of values of the ratio of the support to zeolite diffusion coefficients. We emphasize that the results are specific to the architecture of the supported membranes studied, and thus, the results should be interpreted accordingly.

Microwave synthesis of nanoporous materials.

Studies in the last decade suggest that microwave energy may have a unique ability to influence chemical processes. These include chemical and materials syntheses as well as separations. Specifically, recent studies have documented a significantly reduced time for fabricating zeolites, mixed oxide and mesoporous molecular sieves by employing microwave energy. In many cases, microwave syntheses have proven to synthesize new nanoporous structures. By reducing the times by over an order of magnitude, continuous production would be possible to replace batch synthesis. This lowering of the cost would make more nanoporous materials readily available for many chemical, environmental, and biological applications. Further, microwave syntheses have often proven to create more uniform (defect-free) products than from conventional hydrothermal synthesis. However, the mechanism and engineering for the enhanced rates of syntheses are unknown. We review the many studies that have demonstrated the enhanced syntheses of nanoporous oxides and analyze the proposals to explain differences in microwave reactions. Finally, the microwave reactor engineering is discussed, as it explains the discrepancies between many microwave studies.