Abstract: An ammonia-producing system comprises a reactor that catalytically converts nitrogen and hydrogen feed gases to ammonia to form a reaction mixture of the ammonia, unreacted nitrogen gas, and unreacted hydrogen gas. A feed system feeds the nitrogen and hydrogen gases to the reactor at a reaction pressure of from about 9 to about 100 atmospheres. A reactor control system controls the temperature during conversion of the nitrogen and hydrogen to ammonia by maintaining a reaction temperature of from about 330° C. to about 550° C. An absorbent selectively absorbs at least a portion of the ammonia from the reaction mixture, and an absorbent control system controls one or both of a temperature and pressure at the absorbent during selective absorption of the ammonia from the reaction mixture. A recycle line downstream of the absorbent recycles the unreacted nitrogen and unreacted hydrogen to the reactor.

Abstract: A system for producing ammonia comprises a reactor configured for receiving nitrogen feed gas and hydrogen feed gas, the reactor comprising a catalyst configured to convert at least a portion of the nitrogen gas and at least a portion of the hydrogen feed gas to ammonia to form a reactant mixture comprising the ammonia and unreacted nitrogen feed gas and unreacted hydrogen feed gas, an adsorbent configured to selective adsorb at least a portion of the ammonia from the reactant mixture, and a recycle line to recycle the unreacted nitrogen feed gas, the unreacted hydrogen feed gas, and unabsorbed ammonia to the reactor.

Abstract: An ammonia-producing system comprises a reactor that catalytically converts nitrogen and hydrogen feed gases to ammonia to form a reaction mixture of the ammonia, unreacted nitrogen gas, and unreacted hydrogen gas. A feed system feeds the nitrogen and hydrogen gases to the reactor at a reaction pressure of from about 9 to about 100 atmospheres. A reactor control system controls the temperature during conversion of the nitrogen and hydrogen to ammonia by maintaining a reaction temperature of from about 330° C. to about 550° C. An absorbent selectively absorbs at least a portion of the ammonia from the reaction mixture, and an absorbent control system controls one or both of a temperature and pressure at the absorbent during selective absorption of the ammonia from the reaction mixture. A recycle line downstream of the absorbent recycles the unreacted nitrogen and unreacted hydrogen to the reactor.

Abstract: The present invention provides a method for separation of a targeted molecular species with high purity from a mixture, by controlling temperatures of sublimation unit calculated by a specific formula.

Abstract: A system for producing ammonia comprises a reactor configured for receiving nitrogen feed gas and hydrogen feed gas, the reactor comprising a catalyst configured to convert at least a portion of the nitrogen gas and at least a portion of the hydrogen feed gas to ammonia to form a reactant mixture comprising the ammonia and unreacted nitrogen feed gas and unreacted hydrogen feed gas, an adsorbent configured to selective adsorb at least a portion of the ammonia from the reactant mixture, and a recycle line to recycle the unreacted nitrogen feed gas, the unreacted hydrogen feed gas, and unabsorbed ammonia to the reactor.

Abstract: The present invention relates to a method of removing volatile organic compounds (VOCs) from a latex using a membrane.

Abstract: The present invention relates to a method of removing volatile organic compounds (VOCs) from a latex using a membrane.

Abstract: An osmotic device that, following the imbibement of water vapor, provides for the controlled release of a beneficial agent to an aqueous environment. The device comprises a hydrophilic formulation including a beneficial agent, and if needed, an osmagent, surrounded by a wall. The wall is formed at least in part of a semipermeable hydrophobic membrane having an average pore size between about 0.1 .mu.m and 30 .mu.m. The pores are substantially filled with a gas phase. The hydrophobic membrane is permeable to water in the vapor phase and the hydrophobic membrane is impermeable to an aqueous medium at a pressure less than about 100 Pa. The beneficial agent is released, for example, by osmotic pumping or osmotic bursting upon imbibement of sufficient water vapor into the device core.

Abstract: A process is provided for modifying the properties of a hydrophobic microporous membrane which includes the steps of first providing a hydrophobic microporous membrane, treating it with a surfactant to render the membrane hydrophilic, wetting the membrane with an aqueous solution of a polyol such as polyvinyl alcohol (PVA) and divinyl sulfone (DVS) or a precursor thereof, washing the membrane with water to displace the polyol/DVA from the exterior of the membrane while retaining it in the pores of the membrane, and crosslinking the polyol/DVS into an aqueous gel to yield a hydrophilic microporous membrane having pores filled with an aqueous polyol/DVS gel, the exterior of the membrane being unobstructed by gel. The modified membranes produced according to the process are useful in carrying out chromatographic separations.

Abstract: The rate of mass transfer in liquid/liquid extractions can be increased by the appropriate selection of a solubilizing liquid to wet a microporous membrane. A solute is transferred between immiscible liquids across the membrane where and interface between the liquids is immobilized at a surface of the membrane.

Abstract: Liquid chromatography separations of solutes are achieved using porous hollow fibers. The pores of the hollow fibers immobilize a solute-absorbing phase (preferably organic) which has a greater absorbance affinity towards at least one solute in a mixture of solutes. By passing the solute mixture through the central lumen of the hollow fibers, chromatographic separation are realized due to the greater retention time of that solute with which the immobilized phase has greater absorbance affinity. The immobilized phase may be a liquid organic which may contain a surfactant so as to form reversed micelles or it may be in the form of a polymeric gel. Separations of biological species (e.g., proteins) may thus be accomplished by means of the present invention.

Abstract: Trickle bed reactors are prone to channelling, flooding, and similar flow problems. It has been found that these problems can be avoided by the use of a microporous membrane to separate a reactant fluid phase from a catalysis fluid phase surrounding a catalyst bed. An advantage of such a reactor is that the fluid flows can be separately controlled. An apparatus useful as a trickle bed reactor can include a plurality of microporous hollow fibers arranged in a shell-and-tube configuration within a housing. Such an apparatus is operated with a reactant fluid phase flowing through the fibers and with a catalyst bed on the shell-side of the arrangement.

Abstract: A method for recovery of metal and cyanide from plating baths and rinse waters includes formation of hydrogen cyanide by acid treatment of such solutions, followed by HCN removal through diffusion across a microporous membrane. The method is applicable in a system wherein soluable metal cyanides and metal cyanide complexes are concentrated through use of a basic anion exchange system. Free hydrogen cyanide is released from the anion exchange system by means of an acid regenerant. In a preferred application of the invention, HCN, once having diffused through the microporous membrane, is neutralized with sodium hydroxide, to form a sodium cyanide solution that can be returned to a plating bath.

Abstract: A method is provided for the purification and concentration of soy protein comprising mixing an aqueous solution including soy protein along with other water soluble moieties including sugars, salts, and phytins with a solid crosslinked polymer gel selected from the group consisting of N-substituted polyacrylamides and copolymers of N-substituted polyacrylamides; swelling the gel to absorb a portion of the water and other water soluble moieties including sugars, salts, and phytins from the aqueous solution by substantially maintaining the temperature of the gel at a preselected temperature below the lower critical solution temperature of the gel, to yield a concentrated soy protein solution; and separating the concentrated soy protein solution from the swollen gel. The concentrated soy protein solution may be repeatedly subjected to the gel treatment depending on the desired purity of the protein and the desired solids concentration.

Abstract: A separation method utilizing the ability of temperature-sensitive cross-linked polymer gels to selectively extract solvent from a solution of a macromolecular material. A feed solution containing macromolecules is added to a small amount of gel. The gel swells to absorb the low molecular weight solvent, but it cannot absorb the macromolecules. The raffinate, which is now a concentrated macromolecular solution, is drawn off. To regenerate, the filtered gel is warmed, so that its volume decreases sharply. This suddenly decreased volume occurs because the gel is near a critical point. The solvent is removed from the shrunken gel. The temperature of the gel is then lowered; more feed solution is added; and the cycle is begun again.

Abstract: A separation method utilizing the ability of cross-linked ionic polymer gels to selectively extract solvent from a solution of a macromolecular material. A feed solution containing macromolecules is added to a small amount of basic or warm gel. The gel swells, absorbing the low molecular weight solvent, but cannot absorb the large macromolecules. The raffinate, which is now a concentrated macromolecular solution, is drawn off. To regenerate, a little acid is added to the filtered gel, or the gel is cooled, so its volume decreases sharply. The solvent is expelled from the shrinking gel and is then drawn off, leaving only the collapsed gel. A base is added to the gel, or the gel is warmed. More feed solution is added, and the cycle is begun again.