Abstract: A method for processing biomass to produce biofuel includes decomposing lignocellulosic material into byproduct polymers that include lignin, decomposing the lignin into targeted chemical fragments, and chemically converting the targeted chemical fragments into a biofuel.

Abstract: A method for regenerating at least one impurity-adsorbing sorbent bed includes passing impurity-containing fluid through the impurity-adsorbing bed. The impurity-adsorbing sorbent bed adsorbs an impurity in the impurity-containing fluid to produce a purified fluid. A portion of the purified fluid is sent back through the impurity-adsorbing sorbent bed that contains the adsorbed impurity. The impurity-adsorbing sorbent bed is exposed to microwave energy to desorb the impurity adsorbed on the impurity-adsorbing sorbent bed.

Abstract: A method for processing biomass to produce biofuel includes decomposing lignocellulosic material into byproduct polymers that include lignin, decomposing the lignin into targeted chemical fragments, and chemically converting the targeted chemical fragments into a biofuel.

Abstract: A system and method satisfies temperature and pressure requirements of solid oxide fuel cell system 10 in a manner that increases the overall efficiency and decreases the overall weight of system 10. The system and method include a secondary blower 30 for boosting air stream pressure level sufficient for operation of a reformer 12 that is designed to minimize pressure drop; an integrated heat exchanger 18 for recovering heat from exhaust 36 and comprising multiple flow fields 18A, 18B, 18C for ensuring inlet temperature requirements of a solid oxide fuel cell 14 are met; and a thermal enclosure 46 for separating hot zone 48 components from cool zone 50 components for increasing thermal efficiency of the system and better thermal management.

Abstract: A durable catalyst support/catalyst is capable of extended water gas shift operation under conditions of high temperature, pressure, and sulfur levels. The support is a homogeneous, nanocrystalline, mixed metal oxide of at least three metals, the first being cerium, the second being Zr, and/or Hf, and the third importantly being Ti, the three metals comprising at least 80% of the metal constituents of the mixed metal oxide and the Ti being present in a range of 5% to 45% by metals-only atomic percent of the mixed metal oxide. The mixed metal oxide has an average crystallite size less than 6 nm and forms a skeletal structure with pores whose diameters are in the range of 4-9 nm and normally greater than the average crystallite size. The surface area of the skeletal structure per volume of the material of the structure is greater than about 240 m2/cm3. The method of making and use are also described.

Abstract: A method for regenerating at least one impurity-adsorbing sorbent bed includes passing impurity-containing fluid through the impurity-adsorbing bed. The impurity-adsorbing sorbent bed adsorbs an impurity in the impurity-containing fluid to produce a purified fluid. A portion of the purified fluid is sent back through the impurity-adsorbing sorbent bed that contains the adsorbed impurity. The impurity-adsorbing sorbent bed is exposed to microwave energy to desorb the impurity adsorbed on the impurity-adsorbing sorbent bed.

Abstract: The athermal sorbent bed regeneration system of the present invention includes a main fuel supply, at least one sorbent bed, a source of microwave energy, and a secondary fuel supply. The main fuel supply has a first concentration of an impurity and the secondary fuel supply has a second concentration of the impurity that is less than the first concentration of the impurity. The sorbent bed adsorbs the impurity. The microwave energy source regenerates the sorbent bed for reuse.

Abstract: An apparatus for preferential oxidation of carbon monoxide in a reformate flow includes a reactor defining a flow path for a reformate flow; at least one catalyst bed disposed along the flow path; and a distributor for distributing oxygen from an oxygen source to the at least one catalyst bed, the distributor including a conduit positioned at least one of upstream of and through the at least one catalyst bed, the conduit having a sidewall permeable to flow of oxygen from within the conduit to the at least one catalyst bed.

Abstract: A shift converter, or reactor, (16HT, 16LT) in a fuel processing subsystem (14, 16HT, 16LT, 18), as for a fuel cell (12), uses an improved catalyst bed (34, 50) and the addition of oxygen (40, 40A, 40B, 40C, 40D, 41A, 41B, 41C, 41D) to reduce the amount of carbon monoxide in a process gas stream. The catalyst of bed (34, 50) is a metal, preferably a noble metal, having a promoted support of metal oxide, preferably ceria and/or zirconia. A water gas shift reaction converts carbon monoxide to carbon dioxide. The oxygen may be introduced as air, and causes an improvement in carbon monoxide removal. Use of the added oxygen enables the shift reactor (16HT, 16LT) and its catalyst bed (34, 50) to be relatively more compact for performing a given level of carbon monoxide conversion. The catalyst bed (34, 50) obviates the requirement for prior reducing of catalysts, and minimizes the need to protect the catalyst from oxygen during operation and/or shutdown.

Abstract: An apparatus for preferential oxidation of carbon monoxide in a reformate flow includes a reactor defining a flow path for a reformate flow; at least one catalyst bed disposed along the flow path; and a distributor for distributing oxygen from an oxygen source to the at least one catalyst bed, the distributor including a conduit positioned at least one of upstream of and through the at least one catalyst bed, the conduit having a sidewall permeable to flow of oxygen from within the conduit to the at least one catalyst bed.

Abstract: A shift converter, or reactor, (16HT, 16LT) in a fuel processing subsystem (14, 16HT, 16LT, 18), as for a fuel cell (12), uses an improved catalyst bed (34, 50) and the addition of oxygen (40, 40A, 40B, 40C, 40D, 41A, 41B, 41C, 41D) to reduce the amount of carbon monoxide in a process gas stream. The catalyst of bed (34, 50) is a metal, preferably a noble metal, having a promoted support of metal oxide, preferably ceria and/or zirconia. A water gas shift reaction converts carbon monoxide to carbon dioxide. The oxygen may be introduced as air, and causes an improvement in carbon monoxide removal. Use of the added oxygen enables the shift reactor (16HT, 16LT) and its catalyst bed (34, 50) to be relatively more compact for performing a given level of carbon monoxide conversion. The catalyst bed (34, 50) obviates the requirement for prior reducing of catalysts, and minimizes the need to protect the catalyst from oxygen during operation and/or shutdown.

Abstract: The synthetic porous crystalline material, MCM-56, is synthesized by a process comprising the steps of:a) preparing a reaction mixture containing sources of alkali or alkaline earth metal (M) cation, an oxide of an trivalent element X, an oxide of a tetravalent element Y containing at least 30 wt. % of solid YO.sub.2, a directing agent (R), and water, said reaction mixture having a composition, in terms of mole ratios of oxides, within the following ranges:YO.sub.2 /X.sub.2 O.sub.3 5 to 35H.sub.2 O/YO.sub.2 10 to 70OH.sup.-- /YO.sub.2 0.05 to 0.5M/YO.sub.2 0.05 to 3.0R/YO.sub.2 0.1 to 1.0b) crystallizing said mixture at a temperature of about 80.degree. C. to about 225.degree. C., preferably about 125.degree. C. to about 140.degree. C., to form crystals of MCM-56,c) terminating said crystallization prior to the formation of a significant quantity of MCM-49, andd) separating the MCM-56 crystals from the reaction mixture.

Abstract: A method for synthesizing an ultra-large pore crystalline material which can be used as a sorbent or catalyst component for the conversion of organic and inorganic compounds is improved through the addition of an antifoaming agent. The addition of antifoaming agents reduces foaming without interfering with material synthesis. Elimination of foam allows for easier charging of autoclaves and processing of synthesis mixtures.