Ut-battelle, Inc.

The University of Tennessee Research Foundation

Alliance for Sustainable Energy, LLC

Michael Z Hu

John T Simpson

Mariappan Parans Paranthaman

Tolga Aytug

David W DePaoli

Matthew R Sturgeon

Gyoung Gug Jang

James William Klett

Lonnie J Love

Ilia N Ivanov

Craig A Blue

Thomas T Meek

Chad Edward Duty

Tommy Joe Phelps

Constantinos Tsouris

Saed Mirzadeh

Brian L Bischoff

Chaiwat Engtrakul

Gerald Earle Jellison, Jr

Ronald D Ott

Panos G Datskos

Ji-Won Moon

Joanna McFarlane

Tanya Kuritz

Chad M Parish

Charlee J C Bennett

Quanqin Dai

Steven Walker

Mark F Davis

John W Clavier

Igor Kosacki

Ogbemi Omatete

A solar-thermal vapor-permeation membrane is provided. The solar-thermal vapor-permeation membrane includes a thermally conductive, microporous support layer having a feed surface, and an active separation layer adjacent the feed surface of the support layer. The support layer is capable of absorbing solar-thermal radiation. Utilization of solar energy for a membrane separation process replaces fossil-fuel derived energy with renewable energy as the driving force and does not involve the generation of undesirable greenhouse gas emissions. Therefore, the solar-thermal vapor-permeation process using the provided membrane is cost effective, energy efficient, and environmentally friendly.

Solar-thermal membrane for dewatering aqueous organic-acid solutions

A solar membrane distillation apparatus includes a housing comprising a light transmitting wall. A solar distillation membrane is positioned in the housing to receive solar radiation transmitted through the light transmitting wall. The solar distillation membrane includes a porous graphitic foam and a coating of a hydrophobic composition on the surface and pores of the graphitic foam. A water chamber within the housing is provided for retaining water adjacent to the solar distillation membrane. A vapor chamber is provided for collecting water vapor distilling through the solar distillation membrane. A condenser is provided for condensing distilled water vapor from the vapor chamber into liquid water. A separation membrane and a method of solar distillation are also disclosed.

Superhydrophobic coated micro-porous carbon foam membrane and method for solar-thermal driven desalination

Superhydrophobic membrane structures having a beneficial combination of throughput and a selectivity. The membrane structure can include a porous support substrate; and a membrane layer adherently disposed on and in contact with the porous support substrate. The membrane layer can include a nanoporous material having a superhydrophobic surface. The superhydrophobic surface can include a textured surface, and a modifying material disposed on the textured surface. Methods of making and using the membrane structures.

Super-surface selective nanomembranes providing simultaneous high permeation flux and high selectivity

A method of processing a mixture of heated vapors, at least two of which substantially differ in polarity from each other, the method comprising directing said mixture of heated vapors at a temperature of at least 150&#xb0; C. through a hydrophobic or hydrophilic mesoporous membrane comprising a mesoporous coating of hydrophobized or hydrophilized metal oxide nanoparticles, respectively, wherein the hydrophobic mesoporous membrane permits passage of one or more hydrophobic heated vapors and blocks passage of one or more hydrophilic heated vapors, and wherein the hydrophilic mesoporous membrane permits passage of one or more hydrophilic heated vapors and blocks passage of one or more hydrophobic heated vapors. The method is particularly directed to embodiments where the heated vapors emanate from a pyrolysis process. An apparatus for achieving the above-described method is also described.

Integrated membrane-pyrolysis systems and methods

A method for producing a film, the method comprising melting a layer of precursor particles on a substrate until at least a portion of the melted particles are planarized and merged to produce the film. The invention is also directed to a method for producing a photovoltaic film, the method comprising depositing particles having a photovoltaic or other property onto a substrate, and affixing the particles to the substrate, wherein the particles may or may not be subsequently melted. Also described herein are films produced by these methods, methods for producing a patterned film on a substrate, and methods for producing a multilayer structure.

Methods for producing complex films, and films produced thereby

Applicant's invention is a radionuclide generator resin material for radiochemical separation of daughter radionuclides, particularlyBi, from a solution of parental radionuclides, the resin material capable of providing clinical quantities ofBi of at least 20-mCi, wherein the resin material comprises a silica-based structure having at least one bifunctional ligand covalently attached to the surface of the silica-based structure. The bifunctional ligand comprises a chemical group having desirable surface functionality to enable the covalent attachment of the bifunctional ligand thereon the surface of the structure and the bifunctional ligand further comprises a second chemical group capable of binding and holding the parental radionuclides on the resin material while allowing the daughter radionuclides to elute off the resin material. The bifunctional ligand has a carbon chain with a limited number of carbons to maintain radiation stability of the resin material.

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An ion conducting membrane has a matrix including an ordered array of hollow channels and a nanocrystalline electrolyte contained within at least some or all of the channels. The channels have opposed open ends, and a channel width of 1000 nanometers or less, preferably 60 nanometers or less, and most preferably 10 nanometers or less. The channels may be aligned perpendicular to the matrix surface, and the length of the channels may be 10 nanometers to 1000 micrometers. The electrolyte has grain sizes of 100 nanometers or less, and preferably grain sizes of 1 to 50 nanometers. The electrolyte may include grains with a part of the grain boundaries aligned with inner walls of the channels to form a straight oriented grain-wall interface or the electrolyte may be a single crystal. In one form, the electrolyte conducts oxygen ions, the matrix is silica, and the electrolyte is yttrium doped zirconia.

Design and synthesis of guest-host nanostructures to enhance ionic conductivity across nanocomposite membranes

The present invention comprises a method for fabricating hafnia film comprising the steps of providing a substrate having a surface that allows formation of a self-assembled monolayer thereon via covalent bonding; providing an aqueous solution that provides homogeneous hafnium ionic complexes and hafnium nanoclusters wherein the aqueous solution is capable of undergoing homogeneous precipitation under controlled conditions for a desired period of time at a controlled temperature and controlled solution acidity for desired nanocluster nucleation and growth kinetics, desired nanocluster size, desired growth rate of film thickness and desired film surface characteristics. The method further comprising forming the self-assembled monolayer on the surface of the substrate wherein the self-assembled monolayer comprises a plurality of hydrocarbon chains cross-linked together along the surface of the substrate, the hydrocarbon chains being uniformly spaced from one another and wherein each of the hydrocarbon chains having a functional anchoring group at a first end of the chain covalently bonded with the surface of the substrate and each of the hydrocarbon chains having a functional terminating group projected away from the surface wherein the functional terminating group provides a bonding site for the hafnium film to grow; and exposing the substrate to the aqueous solution for a desired period of time at a controlled temperature wherein the hafnium ionic complexes and the hafnium nanoclusters are deposited on the bonding site of the functional terminating group thereby forming the hafnia film wherein the hafnium bonded to the hydrocarbons and to one another provide a uniform ordered arrangement defined by the uniform arrangement of the hydrocarbons.

Method for fabricating hafnia films

The present invention comprises a method for producing microfibers and nanofibers and further fabricating derived solid monolithic materials having aligned uniform micro- or nanofibrils. A method for producing fibers ranging in diameter from micrometer-sized to nanometer-sized comprises the steps of producing an electric field and preparing a solid precipitative reaction media wherein the media comprises at least one chemical reactive precursor and a solvent having low electrical conductivity and wherein a solid precipitation reaction process for nucleation and growth of a solid phase occurs within the media. Then, subjecting the media to the electric field to induce in-situ growth of microfibers or nanofibers during the reaction process within the media causing precipitative growth of solid phase particles wherein the reaction conditions and reaction kinetics control the size, morphology and composition of the fibers. The fibers can then be wet pressed while under electric field into a solid monolith slab, dried and consolidated.

Production of aligned microfibers and nanofibers and derived functional monoliths

Disclosed is a method for making amorphous spherical particles of zirconium titanate and crystalline spherical particles of zirconium titanate comprising the steps of mixing an aqueous solution of zirconium salt and an aqueous solution of titanium salt into a mixed solution having equal moles of zirconium and titanium and having a total salt concentration in the range from 0.01 M to about 0.5 M. A stearic dispersant and an organic solvent is added to the mixed salt solution, subjecting the zirconium salt and the titanium salt in the mixed solution to a coprecipitation reaction forming a solution containing amorphous spherical particles of zirconium titanate wherein the volume ratio of the organic solvent to aqueous part is in the range from 1 to 5. The solution of amorphous spherical particles is incubated in an oven at a temperature &#x2266;100&#xb0; C. for a period of time &#x2266;24 hours converting the amorphous particles to fine or ultrafine crystalline spherical particles of zirconium titanate.

Method for making fine and ultrafine spherical particles of zirconium titanate and other mixed metal oxide systems

A method for fabricating electronic devices. First, an actinide oxide semiconductor material is provided. Next, an electronic device is fabricated using the actinide oxide semiconductor material.

Fabricating electronic devices using actinide oxide semiconductor materials

Growing community of inventors

Knoxville, TN, United States of America

Michael Z Hu