Compositions for regeneration of spent dialysis fluid are disclosed. The compositions include a sorbent comprising a titanium-glyoxal complex. Sorbent cartridges comprising the sorbents, and methods and systems for using the cartridges in dialysis also are disclosed.

Wet impregnation of active metal precursors into porous substrates, together with selective adsorption of the precursors on the pore surfaces, enables transition metal oxides derived from the precursors to disperse throughout the substrate, even at the nanoscale, without increased sintering or agglomeration, thereby forming oxygen carriers suitable for chemical looping. The porous substrate can be an oxide, for example SiO.sub.2. The oxygen carriers can comprise relatively large oxide loadings of over about 20 wt % and exhibit high reactivity over many regeneration cycles with substantially no loss in oxygen transport capacity or decrease in kinetics. The use of multiple transition metal oxides, for example NiO in addition to CuO, can greatly enhance chemical looping performance.

A separation membrane structure comprises a porous support, a first separation membrane formed on the porous support, and a second separation membrane formed on the first separation membrane. The first separation membrane has an average pore diameter of greater than or equal to 0.32 nm and less than or equal to 0.44 nm. The second separation membrane includes addition of at least one of a metal cation or a metal complex that tends to adsorb nitrogen in comparison to methane.

A superabsorbent polymer composition includes superabsorbent polymer particles, having a crosslinked polymer of water-soluble ethylenically unsaturated monomers including acid groups, of which at least a part are neutralized; and a particulate antimicrobial agent having a quaternary ammonium salt of a silane-based compound. The superabsorbent polymer composition exhibits improved antimicrobial and deodorizing properties without deterioration of the superabsorbent polymer properties such as centrifugal retention capacity.

Method of reducing the arsenic concentration in an aqueous solution comprising undesired arsenic, which method comprises contacting the aqueous solution with a complex of Formula (I), (Formula (I)) wherein M1 and M2 are the same or different and are independently selected from V, Mn, Ga, Cu, Ni, Co, Fe or Zn; wherein a is 0, or 1, and b is 0, or 1, provided that a+b together must be at least 1; Q is a negatively charged counter ion; n is from 1 to 5; X1 is OH, O, SH or S; L1 is a group selected from La1-C(O)NR, La2-C(O)OR, La3-NRC(O), La4-OC(O), La5-O or La6-NRO, wherein La1, La2, La3, La4, La5 and La6 are each C1-6 alkyl, optionally substituted, R is H or C1-6 alkyl optionally substituted; Linker is a polyethylene glycol (PEG) chain with from 1 to 10 repeating units, a C1-16 polyamine chain or a C1-16 alkyl chain; Z is a solid support; L2 to L7 are independently C1-3 alkyl, optionally substituted; and Het1 to Het4 are independently 5 to 14 membered heteroaryl group having at least one N atom and optionally substituted. ##STR00001##

A promoted activated carbon sorbent is described that is highly effective for the removal of mercury from flue gas streams. The sorbent comprises a new modified carbon form containing reactive forms of halogen and halides. Optional components may be added to increase reactivity and mercury capacity. These may be added directly with the sorbent, or to the flue gas to enhance sorbent performance and/or mercury capture. Mercury removal efficiencies obtained exceed conventional methods. The sorbent can be regenerated and reused. Sorbent treatment and preparation methods are also described. New methods for in-flight preparation, introduction, and control of the active sorbent into the mercury contaminated gas stream are described.

A method of treating coal that is combusted in a combustion chamber at a coal-combustion facility that includes adding an additive to the coal for mercury emissions control. The adding of the additive to the coal is performed before the coal enters the combustion chamber. The additive includes Br.sub.2, I.sub.2, a bromide compound, an iodide compound, HBr, HI, or a combination thereof.

A promoted carbon and/or non-carbon base sorbent are described that are highly effective for the removal of mercury from flue gas streams. The promoted sorbent comprises a carbon and/or non-carbon base sorbent that has reacted with and contains forms of halogen and halides. Optional components may be added to increase and/or preserve reactivity and mercury capacity. These may be added directly with the base sorbent, or in-flight within a gas stream (air, flue gas, etc.), to enhance base sorbent performance and/or mercury capture. Mercury removal efficiencies obtained exceed conventional methods. The promoted sorbent can be regenerated and reused. Base sorbent treatment and preparation methods are also described. New methods for in-flight preparation, introduction, and control of the active base sorbent into the mercury contaminated gas stream are described.

Provided are a release resistant moisture absorbent being environment-friendly and having excellent moisture absorbency and release resistance, and a moisture absorbent product comprising the same. The release resistant moisture absorbent of the present invention has an excellent moisture absorption rate, and also excellent release resistance in a high temperature and low humidity condition which is a driving environment of an automobile lamp, and thus, may be usefully used for an automobile lamp.

Metal-containing sorbent materials are provided, methods of making the metal-containing sorbent materials, methods of using the metal-containing sorbent materials, and metal complex-containing composite materials resulting from the sorption of basic, nitrogen-containing compounds on the metal-containing sorbent materials are provided. The sorbent materials are prepared by incorporating divalent metals into a precursor material that is formed by treating a porous siliceous material having mesopores with a silane or disilazane surface treatment agent. The metal-containing sorbent materials can be used to capture basic, nitrogen-containing compounds having a molecular weight no greater than 150 grams/mole.