Measurement standard method

The freezing point measurement, standard method for the detennination of styrene assay until the 1970s, has been largely replaced by gas chromatography. Color is measured spectrophotometrically and registered on the APILA or the platinum-cobalt scale. 

The anionic category represents the major part of surfactant consumption. Anionic surfactants include linear alkylbenzene sulphonates (LASs), alcohol sulphates or alcohol ethersulphates. The latter compounds have a poor absorption in the UV range, whereas the LASs show a significant absorption (see Chapter 11). Dodecylbenzene sulphonate (DBS) is used as a reference for LAS measurements (standard method) and shows an absorption band at 225 nm (Fig. 14). 

ASTM (1985). American Society for Testing and Materials, colour and appearance measurement, standard method for visual evaluation of gloss differences between surfaces of similar appearance. Philadelphia ASTM D 4449-85. 

A visual polythermic method (1) was used as well as an isothermal method which involved conductivity measurements. Standard methods of analysis were used but no specific details are given. 

The criterion retained up to now in the specifications is not the true vapor pressure, but an associated value called the Reid vapor pressure, RVP. The procedure is to measure the relative pressure developed by the vapors from a sample of motor fuel put in a metallic cylinder at a temperature of 37.8°C. The variations characteristic of the standard method are around 15 millibar in repeatability and 25 millibar in reproducibility. 

The water content of crude oils is determined by a standardized method whose procedure is to cause the water to form an azeotrope with an aromatic (generally industrial xylene). Brought to ambient temperature, this azeotrope separates into two phases water and xylene. The volume of water is then measured and compared with the total volume of treated crude. 

The water and sediment contents of crude oils is measured according to the standard methods NF M 07-020, ASTM D 96 and D 1796, which determine the volume of water and sediments separated from the crude by centrifuging in the presence of a solvent (toluene) and of a demulsifylng agent Table 8.13 gives the bottom sediment and water content of a few crude oils. 

The usual practical situation is that in which two solids are bonded by means of some kind of glue or cement. A relatively complex joint is illustrated in Fig. XII-14. The strength of a joint may be measured in various ways. A common standard method is the peel test in which the normal force to separate the joint... 

Several standard methods for the quantitative analysis of food samples are based on measuring the sample s mass following a selective solvent extraction. For example, the crude fat content in chocolate can be determined by extracting with ether for 16 h in a Soxhlet extractor. After the extraction is complete, the ether is allowed to evaporate, and the residue is weighed after drying at 100 °C. This analysis has also been accomplished indirectly by weighing a sample before and after extracting with supercritical GO2. 

Quantitative Analysis for a Single Analyte The concentration of a single analyte is determined by measuring the absorbance of the sample and applying Beer s law (equation 10.5) using any of the standardization methods described in Chapter 5. The most common methods are the normal calibration curve and the method of standard additions. Single-point standardizations also can be used, provided that the validity of Beer s law has been demonstrated. 

Various colorimetric methods have been employed for measuring ozone residuals, although most of these ate susceptible to significant interferences (142). The indigo trisulfonate method (143), however, has been approved by the Standard Methods Committee of the American Pubfle Health Association (141) and the International Ozone Association for ozone residual measurement. 

Color. The visual color, from white to dark brown, of sugar and sugar products is used as a general indication of quaUty and degree of refinement. Standard methods are described for the spectrophotometric deterrnination of sugar color that specify solution concentration, pH, filtration procedure, and wavelength of deterrnination. Color or visual appearance may also be assessed by reflectance measurements. 

A convenient method for assessing the extent of surface oxidation is the measurement of volatile content. This standard method measures the weight loss of the evolved gases on heating up to 950°C in an inert atmosphere. The composition of these gases consists of three principal components hydrogen, carbon monoxide, and carbon dioxide. The volatile content of normal furnace blacks is under 1.5%, and the volatile content of oxidized special grades is 2.0 to 9.5%. 

Surface Area. The most important features influencing the performance of carbon blacks are aggregate size and surface area. Surface area is measured by gas- and Hquid-phase adsorption techniques, and depends on the amount of adsorbate required to form a surface monolayer. If the area occupied by a single-adsorbate molecule is known, a simple calculation will yield the surface area. A low temperature nitrogen absorption method, based on the original method of Bmnauer, Emmett, and Teller (BET) (30), has been adopted by ASTM as standard method D3037-86 (2). 

Quality Control. The spectrometer is the most suitable instmment for determining most low level residual impurities. ASTM E414 is the standard method for the measurement of impurities in copper by the briquette dc-arc technique (65). In this method, the sample in the form of chips, drillings, or powder is briquetted and excited in a d-c arc opposite a high purity copper rod. Impurities in the ranges noted can be measured ... 

Other New Methods. Because the values obtained are dependent on the conditions of measurement, standard test procedures are under review by ISO for determination of cold-water solubiUty of water-soluble dyes (38) determination of the solubiUty and solution stabiUty of water-soluble dyes (39) and determination of the electrolyte stabiUty of reactive dyes (40). 

Vapor-phase decomposition and collection (Figs 4.16 to 4.18) is a standardized method of silicon wafer surface analysis [4.11]. The native oxide on wafer surfaces readily reacts with isothermally distilled HF vapor and forms small droplets on the hydrophobic wafer surface at room temperature [4.66]. These small droplets can be collected with a scanning droplet. The scanned, accumulated droplets finally contain all dissolved contamination in the scanning droplet. It must be dried on a concentrated spot (diameter approximately 150 pm) and measured against the blank droplet residue of the scanning solution [4.67-4.69]. VPD-TXRF has been carefully evaluated against standardized surface analytical methods. The user is advised to use reliable reference materials [4.70-4.72]. 

Because of the complex nature of the discharge conditions, GD-OES is a comparative analytical method and standard reference materials must be used to establish a unique relationship between the measured line intensities and the elemental concentration. In quantitative bulk analysis, which has been developed to very high standards, calibration is performed with a set of calibration samples of composition similar to the unknown samples. Normally, a major element is used as reference and the internal standard method is applied. This approach is not generally applicable in depth-profile analysis, because the different layers encountered in a depth profile of ten comprise widely different types of material which means that a common reference element is not available. 

ASTM E783-84. 1984. Standard Method for Field Measurement of Air Leakage through Installed Exterior Windows and Doors. American Society for Testing and Materials, Philadelphia. 

The goals and the final quantities to be obtained determine the method to be used. As a first approach, it is always worth checking if a documented and proven method exists. Standardized methods are often the best. They are developed by experts in the field and are usually of a high quality and are well documented. Frequently no standards can be applied and generally known methods have to be relied on. Sometimes situations occur when the whole of the measurement procedure has to be tailored for the specific situation. This is a very demanding task and considerable experience is required. 

There is also a standardized method based on the estimation of the flow rate on one measurement point only, In this method the velocity probe is placed in the duct so that the measured local velocity is equal to the mean axial velocity. In fully developed turbulent duct flow, this distance from the wall... 

ASHRAE 41.7-1984. Standard Method for Measurement of Flow of Gas. American Society of Heating, Refrigerating, and Ait-conditioning Engineers, Atlanta, 1984. 

Normally a calibration curve—molar mass against the total retention volume—exists for every GPC column or column combination. As a measure of the separation efficiency of a given column (set) the difference in the retention of two molar masses can be determined from this calibration curve. The same eluent and the same type of calibration standards have to be used for the comparison of different columns or sets. However, this volume difference is not in itself sufficient. In a first approximation the cross section area does not contribute to the separation. Dividing the retention difference by the cross section area normalizes the retention volume for different diameters of columns. The ISO standard method (3) contains such an equation... 

The result of this equation describes the quality of the separation on the basis of an ideal size exclusion mechanism with a given pore volume distribution. The quality of the packing is deliberately excluded from this consideration. This parameter should be measured separately and judged by the plate number. The ASTM standard method for HPSEC of polystyrene (4) contains the following equation for resolution (R,) ... 

Establish standard methods of measurement for source reduction... 

An alternative, total energy, will be used throughout this workbook. The total energy is the heat of a hypothetical reaction that creates a molecule from a collection of separated nuclei and electrons. Like the heat of formation, total energy cannot be measured directly, and is used solely to provide a standard method for expressing and comparing energies. 

Stress birefringence The presence of stress in glass articles may be monitored readily since stressed glass is birefringent. Standard methods exist for these measurements. 

A detailed and well-referenced account of electrochemical methods of testing has been written by Dean, France and Ketcham in a section of the book by Ailor. ASTM G5 1987 outlines standard methods for making potentiostatic and potentiodynamic anodic polarisation measurements and ASTM G3 1974 (R1981) gives conventions applicable to electrochemical measurements in corrosion testing. 

The first instruments used by police to determine BrAc were developed in the 1930s. Until about 1980, the standard method involved adding K O , which reacts chemically with ethyl alcohol. Potassium dichromate has a bright orange-red color, whose intensity fades as reaction occurs. The extent of the color change is a measure of the amount of alcohol present. 

In the internal standard method the intensity of the unknown line is measured relative to that of an internal standard line. The internal line may be a weak line of the main constituent. Alternatively, it may be a strong line of an element known not to be present in the sample and furnished by adding a fixed small amount of a compound of the element in question to the sample. The ratios of the intensities of these lines — the unknown line and the internal standard line — will be unaffected by the exposure and development conditions. This method will provide lines of suitable wavelength and intensity by variations of the added element and the amount added, due regard being paid to the relative volatility of the selected internal standard element. It is important to use as internal standard pairs only those lines of which the relative intensities are insensitive to variations in excitation conditions. The line selected as standard should have a wavelength close to that of the unknown and should, if possible, have roughly the same intensity. 

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