Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Water validation

THE DETERMINATION OF GROSS ALPHA AND GROSS BETA ACTIVITY IN SOLIDS, FILTERS AND WATER - VALIDATION OF DUTCH PRE-NORMS... [Pg.38]

Pinto, G. M. F and I. C. S. F. Jardim. 2000. Use of solid-phase extraction and high performance liquid chromatography for the determination of triazine residues in water validation of the method. J. Chromatogr. A 869(1-2) 463-69. [Pg.816]

Water systems are expected to be demonstrated to be suitable for their intended uses. At a minimum, water is required to meet the World Health Organization requirements for drinking (potable) water. Processing steps such as isolation and purification will require purified water as outlined in USP 23 (2), pharmaceutical grade water. Validation of water systems is required for all product contact water systems. We... [Pg.137]

Eventually, only the drilling of an exploration well will prove the validity of the concept. A wildcat ls drilled in a region with no prior well control. Wells may either result in discoveries of oil and gas, or they find the objective zone water bearing in which case they are termed dry . [Pg.15]

Alternatively, authors have repeatedly invoked the internal pressure of water as an explanation of the rate enhancements of Diels-Alder reactions in this solvent ". They were probably inspired by the well known large effects of the external pressure " on rates of cycloadditions. However, the internal pressure of water is very low and offers no valid explanation for its effect on the Diels-Alder reaction. The internal pressure is defined as the energy required to bring about an infinitesimal change in the volume of the solvents at constant temperature pi = (r)E / Due to the open and... [Pg.20]

The researchers of ECOHYNTOX jointly with the colleagues of the Research Industrial Enterprise Burevestnik (St. Petersburg) have developed, valided, and introduced into practice the methods of inversuve voltampermetric estimation of iodine and selenium in drinking water using AVA-2 apparatus. [Pg.210]

The concentration of salt in physiological systems is on the order of 150 mM, which corresponds to approximately 350 water molecules for each cation-anion pair. Eor this reason, investigations of salt effects in biological systems using detailed atomic models and molecular dynamic simulations become rapidly prohibitive, and mean-field treatments based on continuum electrostatics are advantageous. Such approximations, which were pioneered by Debye and Huckel [11], are valid at moderately low ionic concentration when core-core interactions between the mobile ions can be neglected. Briefly, the spatial density throughout the solvent is assumed to depend only on the local electrostatic poten-... [Pg.142]

The thermodynamic dead volume would be that of a small molecule that could enter the pores but not be retained by differential interactive forces. The maximum retention volume was recorded for methanol and water which, for concentrations of methanol above 10%v/v, would be equivalent to the thermodynamic dead volume for small molecules viz, about 2.8 ml). It is interesting to note that there is no significant difference between the retention volume of water and that of methanol over the complete range of solvent compositions examined, which confirms the validity of this... [Pg.41]

The mobile phase was water in which the moderator alcohols were dissolved. It is seen that the linear relationship is completely validated and the data can provide the adsorption isotherms in the manner discussed. The mean surface area was found to be 199 m /g with a standard deviation between the different alcohols of 11 m /g. [Pg.91]

The above is valid for a liquid flow, when the effect of compressibility can be ignored when calculating gas flows with small pressure differences. For instance, in ventilating duct work, air is not compressed, so the density is considered as constant. In HVAC technology a unit of pressure frequently used for convenience is a water column millimeter, 1 mm H.O=10Pa. [Pg.58]

This shows that the presence of air in the gas phase has a very small influence on the vapor pressure of water. Repeating the same calculation procedure for other temperatures, we can show that the vapor pressure of water can with good accuracy be taken from the vapor pressure tables for saturated water (water has the same pressure as water vapor when they are in equilibrium), as though there were no air in the gas phase. So the vapor pressure of water is with good accuracy also in this case just a function of temperature, and Eq. (4.97) is valid. New vapor pressure tables will not be needed for calculations with humid air. [Pg.71]

When all the water fed to the conditioning chamber vaporizes, the following humidity balance is valid ... [Pg.87]

However, the turbine work has been increased because of the extra water vapour flow through the turbine, while the compressor work is unchanged. Thus Eq. (6.17), which is still valid, with turbine work equal to the heat supplied, shows that the thermal efficiency increases compared with the dry cycle. It is important to realise that this efficiency is increased not because of a reduction in the heat rejected (Qa) but because of the increa.se in Wi- The heat rejected is still equal to the compressor work. [Pg.94]

A further variation of the El-Masri EGT cycle is one in which the evaporation takes place both in an aftercooler and within the cold side of the heat exchanger (Fig. 6.8c). Eq. (6.17) is still valid, but the efficiency is increased because more water can be injected and the turbine work increased further. [Pg.96]

The modeling of a groundwater chemical pollution problem may be one-, two-, or tlu-cc-dimcnsional. The proper approach is dependent on the problem context. For c.xamplc, tlie vertical migration of a chemical from a surface source to the water table is generally treated as a one-dimensional problem. Within an aquifer, this type of analysis may be valid if the chemical nipidly penetrates the aquifer so that concentrations are uniform vertically and laterally. This is likely to be the case when the vertical and latcrtil dimensions of the aquifer arc small relative to the longitudinal scale of the problem or when the source fully penetrates the aquifer and forms a strip source. [Pg.363]


See other pages where Water validation is mentioned: [Pg.366]    [Pg.340]    [Pg.628]    [Pg.356]    [Pg.125]    [Pg.137]    [Pg.366]    [Pg.340]    [Pg.628]    [Pg.356]    [Pg.125]    [Pg.137]    [Pg.337]    [Pg.594]    [Pg.2815]    [Pg.7]    [Pg.120]    [Pg.142]    [Pg.30]    [Pg.36]    [Pg.718]    [Pg.413]    [Pg.378]    [Pg.23]    [Pg.31]    [Pg.383]    [Pg.228]    [Pg.403]    [Pg.359]    [Pg.141]    [Pg.69]    [Pg.48]    [Pg.531]    [Pg.240]    [Pg.347]    [Pg.368]    [Pg.94]    [Pg.122]    [Pg.456]    [Pg.1118]    [Pg.1]   
See also in sourсe #XX -- [ Pg.230 ]




SEARCH



© 2024 chempedia.info