Procedures for determination

Guffey and Wehe (1972) used excess Gibbs energy equations proposed by Renon (1968a, 1968b) and Blac)c (1959) to calculate multicomponent LLE. They concluded that prediction of ternary data from binary data is not reliable, but that quarternary LLE can be predicted from accurate ternary representations. Here, we carry these results a step further we outline a systematic procedure for determining binary parameters which are suitable for multicomponent LLE. 

There are two standard procedures for determining the octane numbers Research or FI and the Motor or F2 methods. The corresponding numbers are designated as RON (Research Octane Number) and MON (Motor Octane Number) which have become the international standard. 

The procedure for determining the cetane number in the CFR engine is not extremely widespread because of its complexity and the cost of carrying it out. There also exist several methods to estimate the cetane number of diesel fuels starting from their physical characteristics or their chemical structure. 

D P f Goodford 1985. A Computational Procedure for Determining Energetically Favorable Binding Sites on Biologically Important Macromolecules. Journal of Medicinal Chemistry 28 849-857. Molecular Discovery Ltd, Oxford, United Kingdom. 

Directions are provided for preparing and using a simple coring device using PVC pipe. This experiment also details a procedure for determining the weight percent of organic material in sediments as a function of depth. 

This experiment describes a simple gravimetric procedure for determining the %w/w Cl in samples of poly(vinyl chloride). 

Method 8.2 describes a procedure for determining Si in ores and alloys. In this analysis a weight loss of 0.21 g corresponds to 0.1 g of Si. Show that this relationship is correct. 

Many pharmaceutical compounds are weak acids or bases that can be analyzed by an aqueous or nonaqueous acid-base titration examples include salicylic acid, phenobarbital, caffeine, and sulfanilamide. Amino acids and proteins can be analyzed in glacial acetic acid, using HCIO4 as the titrant. For example, a procedure for determining the amount of nutritionally available protein has been developed that is based on an acid-base titration of lysine residues. ... 

A procedure for determining the stoichiometry between two reactants by preparing solutions containing different mole fractions of one reactant also known as Job s method. 

Procedures for determining the concentrations of caffeine, benzoic acid and aspartame in soda by these three methods are provided. In the example provided in this paper, the concentrations of caffeine and benzoic acid in Mello Yellow are determined spectrophotometrically. 

The procedure for determining the selection rules for a particular molecule is ... 

Procedures for determining the quaUty of formaldehyde solutions ate outlined by ASTM (120). Analytical methods relevant to Table 5 foUow formaldehyde by the sodium sulfite method (D2194) methanol by specific gravity (D2380) acidity as formic acid by titration with sodium hydroxide (D2379) iron by colorimetry (D2087) and color (APHA) by comparison to platinum—cobalt color standards (D1209). 

Procedures for determining drilling fluid properties ate available (21,22,166). Tests and test methods ate constantly reviewed by API committees to ensure acceptable accuracy when performed under field conditions as well as in the laboratory. API pubHcations ate tepubUshed as new tests ate added or existing tests ate modified. 

In most analytical procedures for determining the total phosphoms content (normally expressed in terms of P20 ), the phosphates are converted to the orthophosphate form. Typically, condensed phosphates are hydrolyzed to orthophosphate by boiling in dilute mineral acid (0.1 N). The orthophosphate is then deterrnined by gravimetric or spectrophotometric methods. For gravimetric deterrnination, insoluble phosphomolybdates (or magnesium ammonium orthophosphate) is formed. 

A widely used procedure for determining trace amounts of selenium involves separating selenium from solution by reduction to elemental selenium using tellurium (as a carrier) and hypophosphorous acid as reductant. The precipitated selenium, together with the carrier, are collected by filtration and the filtered soflds examined directly in the wavelength-dispersive x-ray fluorescence spectrometer (70). Numerous spectrophotometric and other methods have been pubHshed for the deterruination of trace amounts of selenium (71—88). 

Extraction Solvent. Dimethyl sulfoxide is immiscible with alkanes but is a good solvent for most unsaturated and polar compounds. Thus, it can be used to separate olefins from paraffins (93). It is used in the Institute Fransais du Pntrole (IFF) process for extracting aromatic hydrocarbons from refinery streams (94). It is also used in the analytical procedure for determining polynuclear hydrocarbons in food additives (qv) of petroleum origin (95). 

ASTM D629 describes procedures for determining cross-sectional shapes for natural fibers using microscopic analysis. Cross-sectional shape of synthetic fibers also can be verified by using microscopic analysis. 

Source references for frequentiy used test procedures for determining properties of activated carbon are shown in Table 4. A primary source is the Jinnual Book ofyimerican Societyfor Testing and Materials (ASTM) Standards (61). Other usehil sources of standards and test procedures include manufacturers of activated carbon products, the American Water Works Association (AWWA) (33,34), and the Department of Defense (54). 

Procedures for determining ash, moisture, solution preparation, and viscosity measurements can be found in manufacturers product bulletins (40,41) andin ASTMD2364-69 (65). 

Procedures for determining the ash content and moisture level, solution preparation, and viscosity measurement techniques are given in the manufacturer s hterature (50). 

Total acidity and total chlorides can be deterrnined by conventional techniques after hydrolysing a sample. Satisfactory procedures for determining hydrogen chloride and free-sulfiir trioxide are described in the Hterature (18,41). Small amounts of both hydrogen chloride and sulfur trioxide can be found in the same sample because of the equiUbrium nature of the Hquid. Procedures for the direct deterrnination of pyrosulfuryl chloride have also been described (42,43), but are not generally required for routine analysis. Small concentrations of sulfuric acid can be deterrnined by electrical conductivity. 

Static performance measurements related to positioner/ac tuator operation are conformity, measured accuracy, hysteresis, dead baud, repeatability, and locked stem-pressure gain. Definitions and standardized test procedures for determining these measurements can be found in ISA-S75.13-1989, Method of Evaluating the Performance of Positioners with Analog Input Signals and Pneumatic Output . 

An equation for use with venturi meters was given by Chisholm [Br Chem. Eng., 12, 454—457 (1967)]. A procedure for determining steam quahty via pressure-drop measurement with upflow through either venturi meters or sharp-edged orifice plates was given By Colhus and Gacesa [J. Basic Eng., 93, 11-21 (1971)]. 

Particulates Procedures for testing a particulate source are more detailed than those used for sampling gases. Because particulates exhibit inertial effects and are not uniformly distributed within a stack, sampling to obtain a representative sample is more complex than for gaseous pollutants. EPA Method 5 (as shown in Fig. 25-32) is the most widely used procedure for determination of particulate emissions from a stationary source. In-stack samphng guidehnes are presented in EPA Method 17. 

PI Goodford. A computational procedure for determining energetically favorable binding sites on biologically important macromolecules. I Med Chem 28 849-957, 1985. 

ITie BET method is the most widely used procedure for determining the surface area of porous materials. In this chapter, BET results were obtained from single point measurements using a Micromeritics Flowsorb II 2300 surface area analyzer. A mixture of nitrogen in helium (30 70 mole percentage) was used. Although this simple method is not quantitative for the microporous materials studied in section 5, it still allows qualitative comparisons to be made. 

In this reaction, iodine is liberated from a solution of potassium iodide. This reaction can be used to assess the amount of ozone in either air or water. For determination in air or oxygen, a measured volume of gas is drawn through a wash bottle containing potassium iodide solution. Upon lowering the pH with acid, titration is effected with sodium thiosulfate, using a starch solution as an indicator. There is a similar procedure for determining ozone in water. 

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