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Membrane filtration techniques

Anchoring (catalytically active) metal centers to a nanosized dendritic support yields a macromolecular homogeneous catalyst that can be recovered from the product stream by nanofiltration techniques. Moreover, these can, [Pg.6]

A crucial characteristic of a membrane is the molecular weight cutoff (MWCO) value, which is defined as the molecular weight at which 90% of the solutes are retained by the membrane. The retention factor R of solute A to be separated by the membrane is defined by the ratio of the concentration of A in the permeate to that in the retentate, as expressed in the following equation  [Pg.7]

Membrane technology has been performed using either micro-, ultra- or nanofiltration or reverse osmosis in either batch-wise or continuous-flow membrane reactors (CFMR). [Pg.7]

Passive membrane dialysis is usually applied batch-wise, since its driving-force is the difference in gradient concentration between the two solutions separated by the membrane. In this case, the solute (reactants and products small molecules) from a hypertonic solution (the resulting solution of the catalytic reaction) permeates through the membrane to the hypotonic side (pure solvent) until equilibrium has been achieved, whereas the nanosized catalyst remains confined inside the membrane (similar to a tea-bag see Fig. 3A). [Pg.7]

On the other hand, in a CFMR process the particles are transported through the membrane due to the application of a pressure. In this way, the concentrations and residence times of reagents/substrates can be regulated, [Pg.7]


The membrane filtration technique is used once, prior to the introduction of a new disinfectant within the production department. [Pg.196]

All tested organisms showed conform results for (Product Name) using membrane filtration technique and rinsed with 3 x 300 ml of fluid A. [Pg.817]

The purpose is to assure that the recommended disinfectant has the acceptable relative standard of the antimicrobial activity using the membrane filtration technique and surface testing technique. [Pg.843]

The membrane filtration technique is used once, prior to the introduction of a new disinfectant within the production department. The surface testing technique is used prior to any changes in the recommended procedure for evaluating its effectiveness on surfaces to be treated and demonstrating activity against contamination for various contact times. [Pg.843]

Although CFMR experiments have not yet been performed with these met-allodendritic assemblies, their purification using passive dialysis showed the potential application of these catalysts in a recycling process by means of membrane filtration techniques. [Pg.22]

The term bioburden refers to the amount of microbial flora that can be detected on an item or surface or in a solution. The microbial recovery method used depends on the type of material being evaluated. Aerobic bioburden counts in parenteral solutions are obtained by conducting the total aerobic count and total yeast and molds count as specified in the USP microbial limits test (<61>) or a equivalent compendial test. Alternatively, a modified membrane filtration technique can be used to allow filtration of larger volumes of solution to assess bioburden recoveries where sample results are expected to contain a negligible number of microbial flora from the overall solution. [Pg.294]

Size discrimination of insoluble matter may be made to distinguish between finely dispersed, relatively harmless matter and the larger, potentially harmful particles in an oil (ASTM D-4055). The method uses filtration through membranes of known pore size. Membrane filtration techniques are increasingly being used. [Pg.281]

Cross-flow filtration (CFF) also known as tangential flow filtration is not of recent origin. It began with the development of reverse osmosis (RO) more than three decades ago. Industrial RO processes include desalting of sea water and brackish water, and recovery and purification of some fermentation products. The cross-flow membrane filtration technique was next applied to the concentration and fractionation of macromolecules commonly recognized as ultrafiltration (UF) in the late 1960 s. Major UF applications include electrocoat paint recovery, enzyme and protein recovery and pyrogen removal. [Pg.271]

Finally, it is recognized that for short-lived radiopharmaceuticals, the long incubation time of the culture media (7 days for the membrane filtration technique, 14 days for direct inoculation) means the result of the sterility test cannot be available before the product is used. In these situations, the test constitutes a control of production techniques and will give valuable information about their suitability. [Pg.147]

The membrane filtration technique is technically more elaborate and requires that the radiopharmaceutical under test, after aseptic dilution, is passed through a membrane filter with a pore size of 0.45 m, which has been moistened with a sterile nutrient diluent. After filtration, the membrane is either transferred to a suitable culture medium or aseptically cut into two equal parts and one half placed in each of two suitable media. Incubation at the appropriate temperature is required for at least 7 days. [Pg.147]

In BP 1963 there were two important innovations incubation changed from 37 C for 5 days to 30-32 C for 7 days, and a membrane filtration technique was introduced for certain antibiotics. [Pg.22]

Figure 2, Initial NO," transport rate studies in Klebsiella pneumoniae using the membrane filtration technique, showing the binding of N-labeTed nitrate and the subsequent release of it or its metabolic products... Figure 2, Initial NO," transport rate studies in Klebsiella pneumoniae using the membrane filtration technique, showing the binding of N-labeTed nitrate and the subsequent release of it or its metabolic products...
Contrary to the Fuji process, BASF described the characterization and cloning of an L-specific pantolactone hydrolase from Agrobacterium tumefa-ciens [103,104]. This enzyme exclusively opens up the undesired lactone l-1 12, providing a more direct route to d-1 12 (Scheme 35, right side). In addition, this new process is expected to be much more robust toward the competing spontaneous chemical hydrolysis, which could theoretically cause a diminished optical yield in the Fuji process. The enzymatic resolution of d/l-112 in repeated batches with membrane filtration techniques provided d-1 12 in 50% yield and with 90-95% ee. By immobilization onto Eupergit C it was possible to obtain a stable biocatalyst which was easy to use in repeated batch reactions. [Pg.298]

With membrane filtration techniques, analytes can be concentrated on the membranes if the molecular diameter is bigger than that of the pores of the membrane. Analytes are dissolved in a buffer containing ions that are smaller than the pores of the membrane. The buffer ions pass through the membrane, and the analytes with sizes bigger than the membrane pores are concentrated at the membrane. In theory, the degree of concentration is only limited by the ratio of the initial sample volume to the surface of the membrane, and the solubility limit of the samples. [Pg.1403]

Another approach to use the membrane filtration technique in microchips is to integrate the membrane into the separation channel, as Song et al. and Hatch et al. have demonstrated. The chip layout used by Song et al. is given in Figure 50.34a. [Pg.1405]

Elliott J (1996), Membrane filtration techniques in dyestuff recovery , in Reife A, Freeman H S, Environmental chemistry of dyes and pigments. New Y ork, Wiley Interscience Publ, Ch9. [Pg.111]

An account of the changes that have occurred in the HPC methodology in the United States since 1905 can be foimd in Ref. [116]. Many types of media are available for use in determining heterotrophic coimts of flora (Table 4.6) and the three techniques that can be used to determine HPC in water are pour-plate and spread-plate techniques and membrane filtration technique [2]. [Pg.115]

Four methods may be used to detect and enumerate total coliforms, fecal coliforms, and E. coli in water samples. These are grouped as (a) multiple tube fermentation technique also known as the MPN technique, (b) membrane filtration technique, (c) presence/absence test, and (d) use of the enzymatic substrates test also known as the chromogenic-fluorogenic substrate test. [Pg.116]

Selective Media for Enumerating Total Coliforms, Fecal Coliforms, and E. coli Using Membrane Filtration Technique... [Pg.120]

To analyze the aqueous phase for any of these substances, it must first be separated from the polymer particles. Both flocculation and membrane filtration techniques can be used for this purpose and they are described in more detail below. The detection of the substances listed above can then be performed with the usual array of analytical methods used for characterizing aqueous media. For the determination of emulsifiers, electrolytes and water-soluble monomers, ion chromatography (IC) and high-performance liquid chromatography (HPLC) are particularly suitable. The techniques of choice for characterizing oligomers are gel permeation chromatography (GPC) and capillary electrophoresis (CE). As these analytical techniques are not specific to colloidal chemistry, they will not be described further here and the reader should consult the literature for more information. [Pg.57]

A number of researchers have studied high-efficiency membrane filtration techniques as they apply to surfacant micelles. This process is called ultrafiltration, microfiltration, and nanofiltration, depending on the pore size of the membranes. These techniques are applied both to isolation of surfactants themselves and, in micelle enhanced ultrafiltration, to separation of other compounds that are trapped in surfactant micelles so that they are too large to permeate the membrane (99). [Pg.182]


See other pages where Membrane filtration techniques is mentioned: [Pg.50]    [Pg.197]    [Pg.849]    [Pg.50]    [Pg.6]    [Pg.30]    [Pg.33]    [Pg.284]    [Pg.50]    [Pg.125]    [Pg.176]    [Pg.315]    [Pg.22]    [Pg.37]    [Pg.200]    [Pg.840]    [Pg.449]    [Pg.98]    [Pg.119]    [Pg.119]    [Pg.125]    [Pg.58]    [Pg.449]   
See also in sourсe #XX -- [ Pg.58 ]




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