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Water minimization aqueous contamination

Some Practical Considerations in the Use of Salt Bridges. Salt bridges are most commonly used to diminish or stabilize the junction potential between solutions of different composition and to minimize cross-contamination between solutions. For example, in working with nonaqueous solvents an aqueous reference electrode often is used that is isolated from the test solution by a salt bridge that contains the organic solvent. However, this practice cannot be recommended, except on the grounds of convenience, because there is no way at present to relate thermodynamically potentials in different solvents to the same aqueous reference-electrode potential furthermore, there is a risk of contamination of the nonaqueous solvent by water. [Pg.182]

The gap between the glass shde and covershp is filled with aqueous solution, in which the sample may be dissolved or immersed. Since single molecule fluorescence imaging is a kind of extremely low-level light detection, contamination should be as minimized as possible. Hence, the aqueous solutions must be prepared with freshly-purified ultra pure water. The aqueous stock solutions such as the pH buffers and sahnes can be frozen until use in order to eliminate any increase in bacteria. The additives to the aqueous solutions can also influence the background of microscope field. As a pH buffer, we often use phosphate, HEPES, PIPES, citrate, and acetate. [Pg.90]

SCE with carbon dioxide removes organic contaminants and leaves much of the original soil organic matrix in place. The contaminants are then collected on activated carbon in a contaminant collection vessel and transported in an aqueous stream to the WAO reactor for destruction. The concentration of the organic contaminants on activated carbon in water provides a suitable matrix for the WAO feed stream and allows for a smaller reactor size. The activated carbon is then regenerated in the WAO reactor with minimal carbon loss and can be recycled to the contaminant collection vessel. [Pg.698]

Next let us consider those difficulties associated with the determination of the amount of material deposited on the surface. We have already noted that the method of depositing insoluble monolayers by spreading permits the accurate determination of n. Since the spreading technique requires solvent volatility, care must be exercised to prevent the stock solutions from changing concentration due to evaporation prior to their application to the surface. Also, precise microvolumetric methods must be used to dispense the solution on the aqueous surface since the quantity used is small. The solvent (as well as the solute) must be free from contaminants. There is also the possibility that the solvent will extract spreadable contaminants from the waxed surfaces of the float, barriers, and tray. Some workers advocate addition and evaporation of one drop at a time to minimize this. Oily contaminants may also reach the water surface from the fingers and from the atmosphere. These last sources are particularly hard to control Tests for reproducibility and blank compressions (i.e., moving the barrier toward the float on a clean surface) are the best evidence of their absence. [Pg.307]

The process produces no air emissions. Because this is an aqueous-based technology, no NO or SO are produced. The only volatilization of contaminants that occurs is that associated with moving water. A design using laminar flow minimizes loss of organics by this mechanism. [Pg.343]

Preservatives In addition to those processing controls mentioned above (Section 3.1.4.3), the sterility of a product may be maintained through the addition of antimicrobial preservatives. Preservation against microbial growth is an important aspect of multidose parenteral preparations as well as other formulations that require preservatives to minimize the risk of patient infection upon administration, such as infusion products [52], Aqueous liquid products are prone to microbial contamination because water in combination with excipients derived from natural sources (e.g., polypeptides, carbohydrates) and proteinaceous active ingredients may serve as excellent media for the growth [57], The major criteria for the selection of an appropriate preservative include efficiency against a wide spectrum of micro-... [Pg.20]

Sample preparation by means of liquid membrane extraction is a technique that in essence contains two LLE extractions in one step. The setup is easily automated, and sample preparation is performed in a closed system, thus minimizing the risk for contamination and losses during the process. Because the extraction is made from an aqueous phase (donor) to a second, also aqueous phase (acceptor), further enrichment on a precolumn is possible before injection into the LC apparatus. Liquid membranes were used for enrichment of metsulfuron-methyl and chlorsulfuron from clean aqueous samples and natural waters. A similar device was developed by a Chinese... [Pg.951]

Direct Measurement The compound is usually dissolved in octanol, water added, and the system shaken for sufficient time to achieve equihbrium after which the concentration is determined in both phases. Vigorous shaking can introduce errors due to the contamination of the aqueous phase with emulsions and the variation observed with compounds of high Aqw is attributed to this variable. This interference has been minimized using a slow-stirring approach. ... [Pg.41]


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