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Recommended methods

The viscosity is obtained by weighting the viscosities of each component. The recommended method is that of Bromley and Wilke (1951) ... [Pg.143]

C depending on the reference consulted). Fires may be controlled with carbon dioxide or dry chemical extinguishers. Recommended methods of handlings loadings unloadings and storage can be obtained from Material Safety Data Sheets and inquiries directed to suppHers of acetone. [Pg.99]

Initially, there was some ovedap on proposed analytical methods to accomplish a particular analysis. The Association of Official Analytical Chemists (AOAC) methods and Bacteriological Analytical Manual (BAM) methods in some cases dupHcated ASTA methods, but the procedures differed. Most spice companies, particulady those who are members of ASTA, use ASTA recommended methods. In an attempt to ensure that equivalent specifications are reported, the Technical Group of ASTA develops specifications and in some cases recommends that a BAM or AO AC method be used. [Pg.27]

Even though the mechanism of the reaction between oxalate and permanganate is extremely compHcated, titration under acidic conditions is extremely accurate. This is the recommended method for standardi2ation of permanganate solutions. [Pg.524]

Analytical Methods. The official NIOSH recommended method for determining sulfur dioxide in air consists of drawing a known prefiltered volume of air through a bubbler containing hydrogen peroxide, thus oxidising the sulfur dioxide to sulfuric acid. Isopropyl alcohol is then added to the contents in the bubbler and the pH of the sample is adjusted with dilute perchloric acid. The resultant solution is then titrated for sulfate with 0.005 M. barium perchlorate, and Thorin is used as the indicator. [Pg.147]

This is a highly recommended method of capacitor switching for installations that are large and require very fine monitoring and correction of p.f. with the smallest number of banks. The entire reactive requirement is arranged in only a few steps yet a small correction up to the smallest capacitor unit is possible. The relay is sequenced so that through its binary counter the required switching is achieved in small steps, with just four or six sets of capacitor units or banks. The operation of the entire sequence can be illustrated as follows ... [Pg.769]

J.F. Coetzee, Recommended Methods for the Purification of Solvents and Tests for Impurities, Pergamon Press, Oxford, 1982. ISBN 0080223702. [Pg.47]

In addition to the above, purification of /V-methylacetamide can be achieved by fractional freezing, including zone melting, repeated many times, or by chemical treatment with vacuum distn under reduced pressures. For details of zone melting techniques, see Knecht in Recommended Methods for Purification of Solvents and Tests for Impurities, Coetzee Ed. Pergamon Press 1982. [Pg.287]

The propionamide can be dried over CaO. H2O and unreacted propionic acid were removed as their xylene azeotropes. It was vacuum dried. Material used as an electrolyte solvent (specific conductance less than 10 ohm cm" ) was obtained by fractional distn under reduced pressure, and stored over BaO or molecular sieves because it readily absorbs moisture from the atmosphere on prolonged storage. [Hoover Pure Appl Chem 37 581 I974 Recommended Methods for Purification of Solvents and Tests for Impurities, Coetzee Ed., Pergamon Press, 1982.]... [Pg.299]

The recommended method to use to determine the actual theoretical stages at an actual reflux ratio is the Erbar/Maddox relationship. In the graph, N is the theoretical stages and R is the actual reflux ratio L/D, where L/D is the molar ratio of reflux to distillate. N, is the minimum theoretical stages and R, is the minimum reflux ratio. [Pg.52]

A pressure switch located so as to sense falling pressure at the earliest moment should be used to activate the standby pump. The switch should be so connected to the system as to permit testing the startup circuit without shutting down the compressor. Figure 8-8 shows four piping arrangements. The figure at b would be the recommended method. [Pg.313]

A recommended method of characterizing the RTD in flow systems is by using their moments. These are known as the mean, variance, and skewness. The mean value or the centroid of distribution for a concentration versus time curve is... [Pg.676]

The JHA is not a mandatory requirement or a standard, and you are not required to use the recommended methods. It is considered a management tool and a BMP, going beyond the OSHA standard. [Pg.43]

Fcr piping with air in streamline flow at absolute pressures in the range between 50 microns and 1 millimeter of mercury, the following is a recommended method. Calculation procedures in pressure regions below atmospheric are very limited and often not generally applicable to broad interpretations. [Pg.129]

Lubrication. The primary purpose of chain lubrication is to maintain a Film of oil between the bearing surfaces in the joints, thus assuring maximum operating efficiency. This clean oil film must be maintained at all load-carrying points where relative motion occurs, that is, between the pin and bushing on the chain, and the chain and wheel sprocket teeth. Table 3-17 gives some recommended methods for various speeds. [Pg.449]

The method of application is primarily dictated by chain speed and the relative shaft positions. Some recommended methods are given below. [Pg.450]

Helical-lobe compressors are best suited for base-load applications where they can provide a constant volume and pressure of discharge gas. The only recommended method of volume control is the use of variable-speed motors. With variable-speed drives, capacity variations can be obtained with a proportionate reduction in speed. A 50 per cent speed reduction is the maximum permissible control range. [Pg.560]

The difficulties associated with the ASTM Recommended Methods for Detecting Susceptibility to Intergranular Attack in Austenitic Stainless... [Pg.1040]

Recommended methods for assessing the corrosivity of waters, including flowing potable waters, are described in ASTM 02688 1983. Three procedures are described in which test specimens in the form of wires, sheets or tubes are placed in pipes, tanks or other equipment. The test assembly for the first of these consists of three helical wire coils mounted in series on, and electrically insulated from, a supporting frame. The assembly must be installed so that flow is not disturbed and turbulence and high velocities, e.g. of more than 1 -53 ms , are avoided. A minimum test period of 30 days is recommended. Procedures for the other specimen forms are given in the standard. [Pg.1076]

Fig. 3-40 Recommended method for holding metal fittings in thermoformed products. Fig. 3-40 Recommended method for holding metal fittings in thermoformed products.
In most cases diazonium salts are not isolated, but are converted into products by reactions that can be carried out in situ. Moreover, it is actually recommended not to isolate these salts, not even for purification purposes, as many of them have a tendency to explode. In addition, the high solubility of most diazonium salts in water makes precipitation from this medium difficult. Therefore, to obtain solid diazonium salts the recommended method for many decades was to carry out diazotizations in ethanol followed by precipitation with ether. As inorganic salts of nitrous acid are scarely soluble in ethanol, Knoevenagel recommended alkyl nitrites (ethyl or isopentyl nitrite) as diazotization reagents as long ago as 1890. Various other solvents have subsequently been used for diazotizations with alkyl nitrites (see Saunders and Allen, 1985, p. 23 ff.), but as a method for obtaining solid diazonium salts this has been superseded by the isolation of diazonium tetrafluoroborates and, to a lesser degree, of hexafluorophosphates. [Pg.25]

Volume overload employing a solution of the material in the mobile phase at a level of about 5% w/v is a recommended method of sampling for preparative columns if the system is not optimized. However, a combination of volume overload and mass overload has also been suggested as an alternative procedure by Knox (13). [Pg.120]

Methyl parathion was determined in dog and human serum using a benzene extraction procedure followed by GC/FID detection (Braeckman et al. 1980, 1983 DePotter et al. 1978). An alkali flame FID (nitrogen-phosphorus) detector increased the specificity of FID for the organophosphorus pesticides. The detection limit was in the low ppb (pg/L). In a comparison of rat blood and brain tissue samples analyzed by both GC/FPD and GC/FID, Gabica et al. (1971) found that GC/FPD provided better specificity. The minimum detectable level for both techniques was 3.0 ppb, but GC/FPD was more selective. The EPA-recommended method for analysis of low levels (<0.1 ppm) of methyl parathion in tissue, blood, and urine is GC/FPD for phosphorus (EPA 1980d). Methyl parathion is not thermally stable above 120 °C (Keith and Walters 1985). [Pg.175]

Organophosphates, such as methyl parathion, are known to inhibit cholinesterase activity. A method has been developed to measure the extent of this inhibition and relate it to organophosphate exposure (EPA 1980d Nabb and Whitfield 1967). In this EPA-recommended method, blood is separated into plasma and red blood cell fractions. The fractions are treated with saline solution, brought to pH 8 with sodium hydroxide, and dosed with acetylcholine perchlorate. The ensuing acetic acid releasing enzyme reaction... [Pg.177]

Analysis of methyl parathion in sediments, soils, foods, and plant and animal tissues poses problems with extraction from the sample matrix, cleanup of samples, and selective detection. Sediments and soils have been analyzed primarily by GC/ECD or GC/FPD. Food, plant, and animal tissues have been analyzed primarily by GC/thermionic detector or GC/FPD, the recommended methods of the Association of Official Analytical Chemists (AOAC). Various extraction and cleanup methods (AOAC 1984 Belisle and Swineford 1988 Capriel et al. 1986 Kadoum 1968) and separation and detection techniques (Alak and Vo-Dinh 1987 Betowski and Jones 1988 Clark et al. 1985 Gillespie and Walters 1986 Koen and Huber 1970 Stan 1989 Stan and Mrowetz 1983 Udaya and Nanda 1981) have been used in an attempt to simplify sample preparation and improve sensitivity, reliability, and selectivity. A detection limit in the low-ppb range and recoveries of 100% were achieved in soil and plant and animal tissue by Kadoum (1968). GC/ECD analysis following extraction, cleanup, and partitioning with a hexane-acetonitrile system was used. [Pg.181]

Att eZcven y-cJuiin voA nts, discovered thus far, exhibit a change In electrophoretic mobility, and starch gel electrophoresis Is the recommended method for their detection. Quantitation of the variant can best be done by chromatography on columns of either DEAE-Sephadex or CM-Cellulose. The quantities of some variants In heterozygotes differ greatly. For Instance, the relative amount (expressed In %F /Fxotal) varies from 20-25% (F-Malta-I) to 10-15% (most Y C >aln variants) to 5-6%... [Pg.14]

Sterile pharmaceutical preparations must be tested for the presence of fungal and bacterial contamination before use (see Chapters 18 and 23). If the preparation contains an antibiotic, it must be removed or inactivated. Membrane filtration is the usual recommended method. However, this technique has certain disadvantages. Accidental contamination is a problem, as is the retention of the antibiotic on the filter and its subsequent liberation into the nutrient medium. [Pg.486]

The recommended method of trichloroethylene disposal is incineration after mixing with a combustible fuel (Sittig 1985). Care should be taken to carry out combustion to completion in order to prevent the formation of phosgene (Sjoberg 1952). Other toxic byproducts of incomplete combustion include polycyclic aromatic hydrocarbons and perchloroaromatics (Blankenship et al. 1994 Mulholland et al. 1992). An acid scrubber also must be used to remove the haloacids produced. [Pg.201]

Crops, food, and feed. The first recommended method is based on the Dutch Multiresidue Method 2 for A-methylcarbamates, which was originally developed by de Kok et The method has recently been validated by DuPont Crop Protection and Batelle, Geneva Research Centres, for the analysis of methomyl and oxamyl in dry, high-water, high-fat, and high-acid content crops and in various grape processed products. The limit of detection for each analyte is 0.003-0.005 mg kg . ... [Pg.1154]

The European drinking water guidelines set a maximum admissible concentration of 0.10 pgL for individual pesticides and their related compounds in drinking water. The recommended methods for oxime carbamates and their metabolites in groundwater and surface water are suitable for detection limits below 0.10 pgL. The first method is the HPLC/lluorescence multiresidue method of de Kok et al The second method is an HPLC/MS/MS method of DuPont Crop Protection which is specific for oxamyl and may be applicable for the analysis of other oxime carbamates in heavily polluted waters. [Pg.1160]


See other pages where Recommended methods is mentioned: [Pg.143]    [Pg.387]    [Pg.411]    [Pg.254]    [Pg.768]    [Pg.355]    [Pg.239]    [Pg.450]    [Pg.886]    [Pg.78]    [Pg.267]    [Pg.178]    [Pg.192]    [Pg.390]    [Pg.239]    [Pg.550]    [Pg.218]   
See also in sourсe #XX -- [ Pg.127 ]




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