Abstract: In one aspect, TEMPO-cellulose structures and method of making the same are described herein. Briefly, a method of synthesizing TEMPO-cellulose comprises disposing cellulose in an aqueous medium, disposing first and second oxidizing agents in the aqueous medium and oxidizing hydroxyl groups of the cellulose via the first and second oxidizing agents in the presence of a 2,2,6,6-tetramethylpiperidine 1-oxyl radical (TEMPO) catalyst.

Abstract: A cellulose based anti-viral/anti-microbial coating.

Abstract: Electrodeionization apparatuses, systems including a reactor system and an electrodeionization system, and methods of purifying acetic acid are provided herein. In some embodiments, the electrodeionization apparatus includes an anode, and three spaced apart membranes located between the anode and the cathode: a first cation exchange membrane, a first anion exchange membrane, a second cation exchange membrane, defining: a first electrode rinse passage between the anode and the first cation exchange membrane, a first concentrate passage between the first cation exchange membrane and the first anion exchange membrane, a feed stream passage located between the first anion exchange membrane and the second cation exchange membrane, and a second electrode rinse passage between the second cation exchange membrane and the cathode. In some embodiments, the electrodeionization apparatus also includes at least one propionate-selective ion exchange resin wafer within the feed stream passage.

Abstract: In one aspect, TEMPO-cellulose structures and method of making the same are described herein. Briefly, a method of synthesizing TEMPO-cellulose comprises disposing cellulose in an aqueous medium, disposing first and second oxidizing agents in the aqueous medium and oxidizing hydroxyl groups of the cellulose via the first and second oxidizing agents in the presence of a 2,2,6,6-tetramethylpiperidine 1-oxyl radical (TEMPO) catalyst.

Abstract: In one aspect, reverse electrodialysis systems are described herein having constructions operable to reduce membrane stack resistance, thereby requiring significantly less membrane surface area for meaningful electrical power generation. A reverse electrodialysis system described herein comprises an anode and cathode adjacent to a membrane stack, the membrane stack comprising alternating anion and cation exchange membranes defining diluate and concentrate ionic solution compartments, wherein an ion exchange medium is positioned in a diluate compartment.

Abstract: In one aspect, medical implant power sources employing reverse electrodialysis principles are described herein. For example, a power source for a medical implant comprises an anode and cathode adjacent to a membrane stack, the membrane stack comprising alternating anion and cation exchange membranes defining diluate and concentrate fluid compartments. The power source includes a first conduit for delivering a diluate blood stream to the one or more diluate fluid compartments and a second conduit for delivering a concentrate blood stream to the one or more concentrate fluid compartments, wherein the concentrate blood stream has an ionic concentration higher than the diluate blood stream.

Abstract: Electrodeionization apparatuses, systems including a reactor system and an electrodeionization system, and methods of purifying acetic acid are provided herein. In some embodiments, the electrodeionization apparatus includes an anode, and three spaced apart membranes located between the anode and the cathode: a first cation exchange membrane, a first anion exchange membrane, a second cation exchange membrane, defining: a first electrode rinse passage between the anode and the first cation exchange membrane, a first concentrate passage between the first cation exchange membrane and the first anion exchange membrane, a feed stream passage located between the first anion exchange membrane and the second cation exchange membrane, and a second electrode rinse passage between the second cation exchange membrane and the cathode. In some embodiments, the electrodeionization apparatus also includes at least one propionate-selective ion exchange resin wafer within the feed stream passage.

Abstract: Wastewater treatment systems and methods that include a first sub-system that removes suspended solids and free/soluble oil from wastewater and a second sub-system that removes targeted ions or elements from wastewater. Wastewater treatment systems and methods that include an EDI system, including one or more ion exchange wafer configured to selectively remove a specifically targeted ion to a predetermined maximum level of concentration.

Abstract: In one aspect, reverse electrodialysis systems are described herein having constructions operable to reduce membrane stack resistance, thereby requiring significantly less membrane surface area for meaningful electrical power generation. A reverse electrodialysis system described herein comprises an anode and cathode adjacent to a membrane stack, the membrane stack comprising alternating anion and cation exchange membranes defining diluate and concentrate ionic solution compartments, wherein an ion exchange medium is positioned in a diluate compartment.

Abstract: The invention provides a stable concentrated dairy liquid, such as concentrated milk, with improved flavor, color, and mouthfeel, and a method of production thereof. The method utilizes specific thermal treatments to produce the stable concentrated dairy liquid to which a stabilizer and mouthfeel enhancer are added. The resulting products have a sterilization value Fo of at least 5 that is also resistant to gelling and browning during high temperature sterilization and is also resistant to gelling and browning during storage for greater than six months. The method balances such thermal treatments with addition of stabilizer and enhancer to achieve the desired flavor/mouthfeel and sterilization and to achieve reduced level of soluble protein in the concentrated milk prior to concentration to resist gelation and minimize browning. Moreover, such processing may be utilized in a milk that is concentrated to a factor of 2.7 fold or higher and contains at least 8.5 percent protein.

Abstract: The invention provides a stable concentrated dairy liquid, such as concentrated milk, with improved flavor, color, and mouthfeel, and a method of production thereof. The method utilizes specific thermal treatments to produce the stable concentrated dairy liquid to which a stabilizer and mouthfeel enhancer are added. The resulting products have a sterilization value Fo of at least 5 that is also resistant to gelling and browning during high temperature sterilization and is also resistant to gelling and browning during storage for greater than six months. The method balances such thermal treatments with addition of stabilizer and enhancer to achieve the desired flavor/mouthfeel and sterilization and to achieve reduced level of soluble protein in the concentrated milk prior to concentration to resist gelation and minimize browning. Moreover, such processing may be utilized in a milk that is concentrated to a factor of 2.7 fold or higher and contains at least 8.5 percent protein.

Abstract: The invention provides a stable concentrated dairy liquid, such as concentrated milk, with improved flavor, color, and mouthfeel, and a method of production thereof. The method utilizes specific thermal treatments to produce the stable concentrated dairy liquid to which a stabilizer and mouthfeel enhancer are added. The resulting products have a sterilization value Fo of at least 5 that is also resistant to gelling and browning during high temperature sterilization and is also resistant to gelling and browning during storage for greater than six months. The method balances such thermal treatments with addition of stabilizer and enhancer to achieve the desired flavor/mouthfeel and sterilization and to achieve reduced level of soluble protein in the concentrated milk prior to concentration to resist gelation and minimize browning. Moreover, such processing may be utilized in a milk that is concentrated to a factor of 2.7 fold or higher and contains at least 8.5 percent protein.

Abstract: A porous solid ion exchange wafer having a combination of a biomolecule capture-resin and an ion-exchange resin forming a charged capture resin within said wafer. Also disclosed is a porous solid ion exchange wafer having a combination of a biomolecule capture-resin and an ion-exchange resin forming a charged capture resin within said wafer containing a biomolecule with a tag. A separate bioreactor is also disclosed incorporating the wafer described above.

Abstract: The present invention relates to a membrane contactor assisted extraction system and method for extracting a single phase species from multi-phase working solutions. More specifically one preferred embodiment of the invention relates to a method and system for membrane contactor assisted water (MCAWE) extraction of hydrogen peroxide (H2O2) from a working solution.

Abstract: The present invention relates to a process for producing glucosinolates, particularly glucoraphanin, from cruciferous plants. More particularly, a method is provided for producing glucosinolates from agricultural by-products and waste. The general method comprises providing a mixture of glucosinolate-containing plant material and liquid, heating the mixture to inactivate enzymes in the plant material, contacting the heat inactivated mixture with an anion exchange membrane whereby at least a portion of the glucosinolates are extracted from the liquid and absorbed onto the anion exchange membrane, and releasing the glucosinolates from the anion exchange membrane. Preferably, the extraction and release steps are repeated at least once. The glucosinolates produce by the method of the invention may be incorporated into a variety of food products, pharmaceuticals, and health supplements.

Abstract: A porous solid ion exchange wafer having a combination of a biomolecule capture-resin and an ion-exchange resin forming a charged capture resin within said wafer. Also disclosed is a porous solid ion exchange wafer having a combination of a biomolecule capture-resin and an ion-exchange resin forming a charged capture resin within said wafer containing a biomolecule with a tag. A separate bioreactor is also disclosed incorporating the wafer described above.

Abstract: A porous solid ion exchange wafer having a combination of a biomolecule capture-resin and an ion-exchange resin forming a charged capture resin within said wafer. Also disclosed is a porous solid ion exchange wafer having a combination of a biomolecule capture-resin and an ion-exchange resin forming a charged capture resin within said wafer containing a biomolecule with a tag. A separate bioreactor is also disclosed incorporating the wafer described above.

Abstract: The invention provides a stable concentrated dairy liquid, such as concentrated milk, with improved flavor, color, and mouthfeel, and a method of production thereof. The method utilizes specific thermal treatments to produce the stable concentrated dairy liquid to which a stabilizer and mouthfeel enhancer are added. The resulting products have a sterilization value Fo of at least 5 that is also resistant to gelling and browning during high temperature sterilization and is also resistant to gelling and browning during storage for greater than six months. The method balances such thermal treatments with addition of stabilizer and enhancer to achieve the desired flavor/mouthfeel and sterilization and to achieve reduced level of soluble protein in the concentrated milk prior to concentration to resist gelation and minimize browning. Moreover, such processing may be utilized in a milk that is concentrated to a factor of 2.7 fold or higher and contains at least 8.5 percent protein.

Abstract: An electrodialysis system is used to produce reliably, contaminant-free electrodialyzed compositions. A feed stream containing an aqueous solution that has contaminants present is contacted with a membrane electrodialysis system and an electrical potential is applied in an amount effective for recovering the desired aqueous solution without the contaminants while maintaining a higher hydrostatic pressure on the product stream or recovery side.

Abstract: A method of and apparatus for continuously making an organic ester from a lower alcohol and an organic acid is disclosed. An organic acid or salt is introduced or produced in an electrode ionization (EDI) stack with a plurality of reaction chambers each formed from a porous solid ion exchange resin wafer interleaved between anion exchange membranes or an anion exchange membrane and a cation exchange membrane or an anion exchange membrane and a bipolar exchange membranes. At least some reaction chambers are esterification chambers and/or bioreactor chambers and/or chambers containing an organic acid or salt. A lower alcohol in the esterification chamber reacts with an anion to form an organic ester and water with at least some of the water splitting with the ions leaving the chamber to drive the reaction.