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Secondary standard

As a result of a variable liquid-junction potential, the measured pH may be expected to differ seriously from the determined from cells without a liquid junction in solutions of high acidity or high alkalinity. Merely to affirm the proper functioning of the glass electrode at the extreme ends of the pH scale, two secondary standards are included in Table 8.14. In addition, values for a 0.1 m solution of HCl are given to extend the pH scale up to 275°C [see R. S. Greeley, Anal. Chem. 32 1717 (I960)] ... [Pg.931]

The new international temperature scale, known as ITS-90, was adopted in September 1989. However, neither the definition of thermodynamic temperature nor the definition of the kelvin or the Celsius temperature scales has changed it is the way in which we are to realize these definitions that has changed. The changes concern the recommended thermometers to be used in different regions of the temperature scale and the list of secondary standard fixed points. The changes in temperature determined using ITS-90 from the previous IPTS-68 are always less than 0.4 K, and almost always less than 0.2 K, over the range 0-1300 K. [Pg.1214]

The two levels of NAAQS, primary and secondary, are Hsted in Table 3. Primary standards were set to protect pubHc health within an adequate margin of safety secondary standards, where appHcable, were chosen to protect pubHc welfare, including vegetation. According to the CAA, the scientific bases for the NAAQS are to be reviewed every 5 years so that the NAAQS levels reflect current knowledge. In practice, however, the review cycle takes considerably longer. [Pg.368]

Pollutant Averaging time Primary standards Secondary standards... [Pg.2156]

Secondary standard rather than primary standard. [Pg.2157]

The U.S. Clean Air Amendments of 1977 define two kinds of air quality standards primary standards, levels that will protect health but not necessarily prevent the other adverse effects of air pollution, and secondary standards, levels that will prevent all the other adverse effects of air pollution (Table 22-7). The amendments also define air quality levels that cannot be exceeded in specified geographic areas for "prevention of significant deterioration" (PSD) of the air of those areas. Although they are called "increments" over "baseline air quality" in the law, they are in effect tertiary standards, which are set at lower ambient levels than either the primary or secondary standards (Table 22-8). [Pg.377]

Primary Standard a pollution standard based on human health effects. Primary standards are set for criteria air pollutants. See also secondary standard. [Pg.543]

A National Secondary Drinking Water Regulation (NSDWR or secondary standard) is a non-enforceable guideline regarding contaminants that may cause cosmetic effects (such as skin or tooth discoloration) or aesthetic effects (such as taste, odor, or color) in drinking water. EPA recommends secondary standards to water systems but does not require systems to comply. However, states may choose to adopt them as enforceable standards. This information focuses on national primary standards. [Pg.11]

The Safe Drinking Water Act protects the quality of drinking water in the IJ.S. This law focu.ses on all waters actually or potentially designated for drinking use, whether above or below ground. The Act authorized EPA to establish safe standards of purity and required all owners or operators of public water systems to comply with primary (health-related) standards. State governments, that assume this power from EPA, also encourage attainment of secondary standards (nuisance-related). [Pg.26]

Electrostatic and adsorption effects conspire to make aqueous GPC more likely to be nonideal than organic solvent GPC. Thus, universal calibration is often not obeyed in aqueous systems. Elence, it is much more critical that the standard chosen for calibration share with the polymer being analyzed chemical characteristics that affect these interactions. Because standards that meet this criterion are often not available, it is prudent to include in each analysis set a sample of a secondary standard of the same composition and molecular weight as the sample. Thus, changes in the chromatography of the analyte relative to the standards will be detected. [Pg.557]

Alternatively, either the Elamielec or the integral broad standard calibration procedure can be used. For this approach, the broad standard would be initially analyzed using a calibration based on some convenient standard that may be quite dissimilar in chemistry from the standard. From that point forward, the system is calibrated with the secondary standard. Thus, changes that affect the sample will be compensated for in the calibration procedure. [Pg.557]

Z values are obtained from Eq. (8-76) for solvents having Z in the approximate range 63-86. In more polar solvents the CT band is obscured by the pyridinium ion ring absorption, and in nonpolar solvents l-ethyl-4-carbomethoxy-pyridinium iodide is insoluble. By using the more soluble pyridine-1-oxide as a secondary standard and obtaining an empirical equation between Z and the transition energy for pyridine-1-oxide, it is possible to measure the Z values of nonpolar solvents. The value for water must be estimated indirectly from correlations with other quantities. Table 8-15 gives Z values for numerous solvents. [Pg.437]

The EPA sets two kinds of national ambient air quality standards. The primary standard is set at a level intended to protect human health with an adequate margin of safety. The secondary standard, usually less stringent, is set based on protecting the public welfare, which can include factors other than health impacts, such as reduced visibility, atid damage to crops. [Pg.51]

Pollutant Primary Standard (Health Related) Secondary Standard (Welfare Related)... [Pg.52]

CO 8-hour 1-hour 9 parts per million 35 parts per million No secondary standard No secondary standard... [Pg.52]

For scientific work the fundamental standard of mass is the international prototype kilogram, which is a mass of platinum-iridium alloy made in 1887 and deposited in the International Bureau of Weights and Measures near Paris. Authentic copies of the standard are kept by the appropriate responsible authorities in the various countries of the world these copies are employed for the comparison of secondary standards, which are used in the calibration of weights for scientific work. The unit of mass that is almost universally employed in laboratory work, however, is the gram, which may be defined as the one-thousandth part of the mass of the international prototype kilogram. [Pg.75]

The IUPAC Commission on Analytical Nomenclature refers to (3) and (4) respectively as Primary Standard Solutions and Secondary Standard Solutions. [Pg.107]

Comparative method. Sometimes, as in the analysis of a mineral, it may be impossible to prepare solid synthetic samples of the desired composition. It is then necessary to resort to standard samples of the material in question (mineral, ore, alloy, etc.) in which the content of the constituent sought has been determined by one or more supposedly accurate methods of analysis. This comparative method, involving secondary standards, is obviously not altogether satisfactory from the theoretical standpoint, but is nevertheless very useful in applied analysis. Standard samples can be obtained from various sources (see Section 4.5). [Pg.129]

In titrimetry certain chemicals are used frequently in defined concentrations as reference solutions. Such substances are referred to as primary standards or secondary standards. A primary standard is a compound of sufficient purity from which a standard solution can be prepared by direct weighing of a quantity of it, followed by dilution to give a defined volume of solution. The solution produced is then a primary standard solution. A primary standard should satisfy the following requirements. [Pg.261]

Hydrated salts, as a rule, do not make good standards because of the difficulty of efficient drying. However, those salts which do not effloresce, such as sodium tetraborate Na2B407, 10H2O, and copper sulphate CuS04,5H20, are found by experiment to be satisfactory secondary standards.2... [Pg.262]

A secondary standard is a substance which may be used for standardisations, and whose content of the active substance has been found by comparison against a primary standard. It follows that a secondary standard solution is a solution in which the concentration of dissolved solute has not been determined from the weight of the compound dissolved but by reaction (titration) of a volume of the solution against a measured volume of a primary standard solution. [Pg.262]

The standardisation of thiosulphate solutions may be effected with potassium iodate, potassium dichromate, copper and iodine as primary standards, or with potassium permanganate or cerium)IV) sulphate as secondary standards. Owing to the volatility of iodine and the difficulty of preparation of perfectly pure iodine, this method is not a suitable one for beginners. If, however, a standard solution of iodine (see Sections 10.112 and 10.113) is available, this maybe used for the standardisation of thiosulphate solutions. [Pg.391]

Titrimetric analysis - continued general discussion of, 257 primary and secondary standards for, 261 storage and preservation of solutions, 108 technique of, 286... [Pg.876]

In a multi-year, multi-laboratory situation it is unlikely that the amount of primary standard (PS) will suffice to cover all requests. The next best thing is to calibrate a larger amount of lower-quality secondary standard (SS) against the PS, and to repeat the calibration at specified intervals until both the PS and the SS have been consumed. In this way, consistency can be upheld until a new lot of PS has been prepared and cross-validated against the previous one. In practice, a working standard will be locally calibrated against the SS and be used for the daily method calibration runs. (See Section 4.32.)... [Pg.256]


See other pages where Secondary standard is mentioned: [Pg.1248]    [Pg.717]    [Pg.932]    [Pg.327]    [Pg.465]    [Pg.378]    [Pg.26]    [Pg.366]    [Pg.1125]    [Pg.340]    [Pg.261]    [Pg.261]    [Pg.370]    [Pg.432]    [Pg.870]    [Pg.362]    [Pg.248]    [Pg.305]    [Pg.306]    [Pg.307]    [Pg.281]    [Pg.283]    [Pg.290]   
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See also in sourсe #XX -- [ Pg.152 ]

See also in sourсe #XX -- [ Pg.136 , Pg.137 ]

See also in sourсe #XX -- [ Pg.89 ]




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