Articles are treated with a reduced amount of a halo active aromatic sulfonamide compound of Formula (I): ##STR00001##
wherein R.sub.1, R.sub.2, R.sub.3, R.sub.4, and R.sub.5 are independently selected from hydrogen, COOR, CON(R).sub.2, alkoxy, CN, NO.sub.2, SO.sub.3R, halogen, substituted or unsubstituted phenyl, sulfonamide, halosulfonamide, and substituted or unsubstituted C.sub.1-C.sub.12 alkyl; R is hydrogen, an alkali metal, an alkaline earth metal, substituted C.sub.1-C.sub.12 alkyl, or unsubstituted C.sub.1-C.sub.12 alkyl; and R is hydrogen or substituted or unsubstituted C.sub.1-C.sub.12 alkyl, where the two R groups in CON(R).sub.2 may be independently selected; X is halogen; M is an alkali or alkaline earth metal; and n is the number of water molecules per molecule of the sulfonamide compound. The compound effectively suppresses odors pre-use, in use, and post-use for extended periods of time.

The present invention provides for the use of a metal-organic framework (MOF) in removing particular chemical species or compounds, in particular oxy-anions, from a liquid or liquid stream. In some embodiments, the MOF is a Zr-based MOF, such as NU-1000, and the oxy-anions that are removed include, include, for example, oxy-anions of selenium, including selenite (SeO.sub.3.sup.2) and selenate (SeO.sub.4.sup.2); oxy-anions of antimony, including oxy-anions in either the Sb[III] (antimonite) or the Sb[V] (antimonate) redox state; and oxy-anions of lead, including oxy-anions in either the Pb[II] or the Pb[IV] redox state, such as Pb(OH).sub.6.sup.2, Pb(OH).sub.6.sup.4, PbO.sub.3.sup.2, and PbO.sub.2.sup.2. The Zr-based MOF, including NU-1000 can be used to remove these oxy-anions from various liquid streams in industrial processes such as a nuclear and fossil fuel power plants, including the latter's flue gas desulfurization system.

A detachable module for optionally recharging sorbent materials, including zirconium phosphate, with an optional bypass and conduits for a sorbent cartridge. The sorbent cartridge can have one or more modules contained therein having connectors connecting each of the modules. One or more of the modules can be reusable and the sorbent materials therein recharged.

A method for separating and purifying recombinant human serum albumin (rHSA) from transgenic rice grain, sequentially comprising the steps of: 1) subjecting crude extract of rHSA to cation exchange chromatography to obtain primary product I; 2) subjecting the primary product I to anion exchange chromatography to obtain secondary product II; 3) subjecting the secondary product II to hydrophobic chromatography to obtain purified rHSA. The method may further comprise a step of ceramic hydroxyapatite chromatography prior to the hydrophobic chromatography. The method has the advantages of low cost and easy operation. The resultant rHSA has a purity of about 99% by HPLC.

Provided are graft copolymer particles enabling introduction of adsorptive functional groups adsorbing metals and others, a method for producing same, and an adsorbent using same. (1) Porous graft copolymer particles containing graft chains introduced into porous particles (particle surface having an average pore diameter of 0.01-50 ?m) including at least one resin selected from olefin resins, water-insoluble modified polyvinyl alcohol resins, amide resins, cellulosic resins, chitosan resins and (meth)acrylate resins. (2) A method for producing porous graft copolymer particles including (I) melt-kneading a polymer A and a polymer B other than the polymer A to obtain a compound material, (II) extracting and removing the polymer B from the compound material to obtain a porous material of the polymer A, (III) granulating the porous material, and (IV) introducing graft chains into the porous particles. (3) An adsorbent of porous graft copolymer particles.

A device and method for preparing in-situ molded biochar with high specific surface area. Crushed and mixed biomass and modifier are fed into a hot pressing and pyrolysis device, and hot-pressing molding and pyrolysis carbonization are completed synchronously, which solves the problem of multiple steps and complicated equipment in the existing preparation process for molded biochar material. In-situ bonding molding is realized by adhesion, bridging, cross-linking and mechanical interlocking functions of low-temperature molten & softened lignin and pyrolytic tar. No additional cross-linking agent is needed in this process, so the production cost is low. Covering and suffocating actions of trace flame retardant modifier are utilized to reduce the temperature of biomass pyrolysis carbonization, inhibit excessive ablation and accelerate polycondensation reaction, thus to improve the specific surface area and yield of a product, and improve the cost performance of the product.

A monolith for catalytic or sorbent purposes. The monolith includes a substrate sheet having attached thereto a plurality of catalytic or sorbent beads. Each bead has a diameter of at least fifty microns. The substrate sheet at least partially defines one or more channels through the monolith. Fluid flowing through the channels will contact the beads for catalytic or sorbent purposes.

A detachable module for optionally recharging sorbent materials, including zirconium phosphate, with an optional bypass and conduits for a sorbent cartridge. The sorbent cartridge can have one or more modules contained therein having connectors connecting each of the modules. One or more of the modules can be reusable and the sorbent materials therein recharged.

A measuring instrument for detection of electrical properties in a liquid includes a main body configured to hold a tester, a first pole extending from the main body, and a second pole extending from the main body that is spaced apart from the first pole. The first pole carries a positive probe for attachment to the tester, and the second pole carries a negative probe for attachment to the tester. When the probes are placed in the liquid, electrical properties in the liquid are detected by the tester.

A method for enhancing sorption performance of a sorbent material includes the step of increasing a surface area of the sorbent material for adsorption of a fluid at an interface between the fluid and the sorbent material by arranging one or more apertures to be disposed on the sorbent material, wherein each of the one or more apertures is further arranged to define an interior space for absorption of the fluid.