Chemical preparation techniques water

Metal organic decomposition (MOD) is a synthesis technique in which metal-containing organic chemicals react with water in a nonaqueous solvent to produce a metal hydroxide or hydrous oxide, or in special cases, an anhydrous metal oxide (7). MOD techniques can also be used to prepare nonoxide powders (8,9). Powders may require calcination to obtain the desired phase. A major advantage of the MOD method is the control over purity and stoichiometry that can be achieved. Two limitations are atmosphere control (if required) and expense of the chemicals. However, the cost of metal organic chemicals is decreasing with greater use of MOD techniques. 

Sample preparation techniques vary depending on the analyte and the matrix. An advantage of immunoassays is that less sample preparation is often needed prior to analysis. Because the ELISA is conducted in an aqueous system, aqueous samples such as groundwater may be analyzed directly in the immunoassay or following dilution in a buffer solution. For soil, plant material or complex water samples (e.g., sewage effluent), the analyte must be extracted from the matrix. The extraction method must meet performance criteria such as recovery, reproducibility and ruggedness, and ultimately the analyte must be in a solution that is aqueous or in a water-miscible solvent. For chemical analytes such as pesticides, a simple extraction with methanol may be suitable. At the other extreme, multiple extractions, column cleanup and finally solvent exchange may be necessary to extract the analyte into a solution that is free of matrix interference. 

Hydride generation AAS is a well-established technique for the determination of selenium because of its selectivity and sensitivity. The detection limits are improved by concentrating the hydride prior to the transfer to the spectrometer. Cryogenic condensation in a U-tube at liquid nitrogen temperature is a preferred method of pre-concentration. However, selenium hydride is formed essentially only from Se. The selectivity for Se has been combined with various chemical preparation steps to determine the sum of SeIV and Se and the total selenium content of samples. Se concentrations are measured by the difference between the (Se + Se ) and Se contents. The difference between total selenium and (Se + Se ) contents represents the concentrations of Se° and Se2- species. These methods have been used for determinations of selenium species in natural waters. Soluble organic matter in some groundwater samples interferes with the hydride generation determination of selenium. Isolation of humic substances by their adsorption on resins has overcome this problem. 

Nanostructures primarily result from polyelectrolyte or interpolyelectrolyte complexes (PEC). The PEC (also referred to as symplex [23]) is formed by the electrostatic interaction of oppositely charged polyelectrolytes (PE) in solution. The formation of PEC is governed by physical and chemical characteristics of the precursors, the environment where they react, and the technique used to introduce the reactants. Thus, the strength and location of ionic sites, polymer chain rigidity and precursor geometries, pH, temperature, solvent type, ionic strength, mixing intensity and other controllable factors will affect the PEC product. Three different types of PEC have been prepared in water [40] (1) soluble PEC (2) colloidal PEC systems, and (3) two-phase systems of supernatant liquid and phase-separated PEC. These three systems are respectively characterized as ... 

Cu-exchanged zeolite catalyst containing strong water tolerance and hydrothermal stability, although a method for preparation by using a solid ion exchange chemical transport technique has been suggested. 

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