Method of determinants

The University developed a method of determination of the material residual strength, based on measurement of the change of phase velocity of ultrasonic waves, as well as an ultrasonic flaw detector-tomograph with multi-element transducers of the type of phased acoustic array. It enables control of the internal structure of materials and products of up to 300 mm thickness, with the resolution of up to 0.5 mm. In the same university, work on NDT is also carried out in the welding and electro-acoustic departments. 

Millikan R A A new modification of the cloud method of determining the elementary electrical charge and the most probable value of that charge Phil. Mag. 19 209-28... 

A completely new method of determining siufaces arises from the enormous developments in electron microscopy. In contrast to the above-mentioned methods where the surfaces were calculated, molecular surfaces can be determined experimentally through new technologies such as electron cryomicroscopy [188]. Here, the molecular surface is limited by the resolution of the experimental instruments. Current methods can reach resolutions down to about 10 A, which allows the visualization of protein structures and secondary structure elements [189]. The advantage of this method is that it can be apphed to derive molecular structures of maaomolecules in the native state. 

The conditloci to be satisfied by the pressure difference, if (10,18) is to be a good approximation, is not so demanding as that needed to ensure that (10.14) is a good approximation, and it does not depend on the permeability of the medium. Thus (10.18), applied at sufficiently high pressure, should provide a method of determining which is more robust than (10.14)... 

An alternative method of determining the completion of the reaction is to weigh the flask cmd toluene, emd to stop the passage of chlorine when the increase in weight is 37 g. 

In determining the values of Ka use is made of the pronounced shift of the UV-vis absorption spectrum of 2.4 upon coordination to the catalytically active ions as is illustrated in Figure 2.4 ". The occurrence of an isosbestic point can be regarded as an indication that there are only two species in solution that contribute to the absorption spectrum free and coordinated dienophile. The exact method of determination of the equilibrium constants is described extensively in reference 75 and is summarised in the experimental section. Since equilibrium constants and rate constants depend on the ionic strength, from this point onward, all measurements have been performed at constant ionic strength of 2.00 M usir potassium nitrate as background electrolyte . 

For hquid systems v is approximately independent of velocity, so that a plot of JT versus v provides a convenient method of determining both the axial dispersion and mass transfer resistance. For vapor-phase systems at low Reynolds numbers is approximately constant since dispersion is determined mainly by molecular diffusion. It is therefore more convenient to plot H./v versus 1/, which yields as the slope and the mass transfer resistance as the intercept. Examples of such plots are shown in Figure 16. 

Black Powder. Black powder is mainly used as an igniter for nitrocellulose gun propellant, and to some extent in safety blasting fuse, delay fuses, and in firecrackers. Potassium nitrate black powder (74 wt %, 15.6 wt % carbon, 10.4 wt % sulfur) is used for military appHcations. The slower-burning, less cosdy, and more hygroscopic sodium nitrate black powder (71.0 wt %, 16.5 wt % carbon, 12.5 wt % sulfur) is used industrially. The reaction products of black powder are complex (Table 12) and change with the conditions of initia tion, confinement, and density. The reported thermochemical and performance characteristics vary greatly and depend on the source of material, its physical form, and the method of determination. Typical values are Hsted in Table 13. 

The preferred method of determining water in glycerol is by the Kad Fischer volumetric method (18). Water can also be determined by a special quantitative distillation in which the distilled water is absorbed by anhydrous magnesium perchlorate (19). Other tests such as ash, alkalinity or acidity, sodium chloride, and total organic residue are included in AOCS methods (13,16,18). 

Quantitative Analysis of All llithium Initiator Solutions. Solutions of alkyUithium compounds frequentiy show turbidity associated with the formation of lithium alkoxides by oxidation reactions or lithium hydroxide by reaction with moisture. Although these species contribute to the total basicity of the solution as determined by simple acid titration, they do not react with allyhc and henzylic chlorides or ethylene dibromide rapidly in ether solvents. This difference is the basis for the double titration method of determining the amount of active carbon-bound lithium reagent in a given sample (55,56). Thus the amount of carbon-bound lithium is calculated from the difference between the total amount of base determined by acid titration and the amount of base remaining after the solution reacts with either benzyl chloride, allyl chloride, or ethylene dibromide. 

Mineral and Chemical Composition. X-ray diffraction is used to determine the mineral composition of an Mg(OH)2 sample. Induced coupled plasma (icp) spectrophotometry is used to measure the atomic concentrations present in a sample. X-ray fluorescence analysis is another comparative instmmental method of determining chemical composition. 

An inventor may estabHsh utiHty by providing several working examples which disclose preparation, appHcation, and even some or all of the benefits of the invention. UtiHty may also be substantiated by merely disclosing several appHcations for the invention. One method of determining the breadth or scope of an invention is to define the invention by only those elements essential to performing the intended task. This definition should then become the broadest cl aim of the patent appHcation. 

Thermal decomposition of perchlorate salts to chloride, followed by the gravimetric determination of the resulting chloride, is a standard method of determining quantitatively the concentration of perchlorates. Any chlorates that are present in the original sample also break down to chloride. Thus results are adjusted to eliminate errors introduced by the presence of any chlorides and chlorates in the original sample. 

Optical properties of fibers are measured by light microscopy methods. ASTM D276 describes the procedure for fiber identification using refractive indexes and birefringence. Other methods for determining fiber optical properties have been discussed (3,38—44). However, different methods of determining optical properties may give different results (42). 

As computing capabiUty has improved, the need for automated methods of determining connectivity indexes, as well as group compositions and other stmctural parameters, for existing databases of chemical species has increased in importance. New naming techniques, such as SMILES, have been proposed which can be easily translated to these indexes and parameters by computer algorithms. Discussions of the more recent work in this area are available (281,282). SMILES has been used to input Contaminant stmctures into an expert system for aquatic toxicity prediction by generating LSER parameter values (243,258). 

The lower Emit of applicability of the nucleate-boiling equations is from 0.1 to 0.2 of the maximum limit and depends upon the magnitude of natural-convection heat transfer for the liquid. The best method of determining the lower limit is to plot two curves one of h versus At for natural convection, the other ofh versus At for nucleate boiling. The intersection of these two cui ves may be considered the lower limit of apphcability of the equations. 

In the first case, the annual taxable income is reduced by an annual depreciation charge or allowance which has the effect of reducing the annual amount or tax payable. The annual depreciation charge is merely a book transac tion and does not involve any expenditure of cash. The method of determining the annual depreciation charge must be agreed to by the appropriate tax authority. 

Figure 12-25 provides a rapid method of determining the pond-area requirements for a given coohng duty. Di and Do are the approaches to equilibrium for the entering and leaving water, °F V Js trie wind velocity, mFh product PQ represents the area of the pond surface, ft /(gal-min) of flowto thepond. The P factor assumes a pond with uniform flow, without turbulence, and with the water warmer than the air. 

One of the most required methods of determination of iodide-ions in praetiee of ehemieal analysis is photometrie determination of produets of iodination of organie eompounds. The oxidation of iodide to iodine ean be earned out suffieiently seleetively. But in ease of presenee of great abundanee of bromide-ions the seleetive oxidation of iodide-ions is problematie. The variants of determination of iodide-ions with different organie reagents are known, but the absenee of bromide-ions in a system is supposed in most of them. In natural objeets these halides are present simultaneously. 

The seleetive method of determination of iodide-ions in the bromide-prevalenee systems is suggested. The variant is realized this way ... 

The comparison of analytical characteristics HPLC methods of determination of phenols with application amperometric and photometric detectors was caiiy out in this work. Experiment was executed with use liquid chromatograph Zvet-Yauza and 100 mm-3mm 150mm-3mm column with Silasorb C18 (5 10 p.m). With amperometric detector phenols were detected in oxidizing regime on glass-cai bon electrodes. With photometric detector phenols were detected at 254 nm. 

A series of techniques of determination 2,4-D is known. However, there is an actual problem of development of express and semiquatitative methods of determination, which would allow to monitor fastly the content of this herbicide, both in lab and in field conditions. 

NEW APPROACH TO INCREASING OF ROBUSTNESS FOR METHOD OF DETERMINATION OF MOLECULAR WEIGHT DISTRIBUTION IN DEXTRANS... 

Highly sensitive methods of determination of natural objects stmcture lead to a lai ge amount of data on the content of elements in different natural objects, such as rocks, soils, minerals, natural water, alive organisms, meteorites etc. 

EPA (Environmental Protection Agency). 1980. A Method of Determining the Compatibility of Hazardous Wastes. EPA Report No. EPA-600/2-80-076. Municipal Environmental Research Eaboratory, Environmental Research Eaboratory, Environmental Protection Agency, Cincinnati, Ohio. 

Specify the yield ratio or method of determining the yield ratio. 

These should normally be used in a box form for better mounting, uniformity and metal utilization. The method of determining the reactance for single- and three-phase systems is the same as for rectangular sections (Figure 28.20(a)). 

Another important method of determining the Gruneisen ratio in the shock state is the measurement of sound speed behind the shock front. The techniques employing optical analyzers (McQueen et al., 1982) piezoresistive (Chap-... 

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