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Experimental methods for

The most widely used experimental method for determining surface excess quantities at the liquid-vapor interface makes use of radioactive tracers. The solute to be studied is labeled with a radioisotope that emits weak beta radiation, such as H, C, or One places a detector close to the surface of the solution and measures the intensity of beta radiation. Since the penetration range of such beta emitters is small (a ut 30 mg/cm for C, with most of the adsorption occurring in the first two-tenths of the range), the measured radioactivity corresponds to the surface region plus only a thin layer of solution (about 0.06 mm for C and even less for H). [Pg.77]

With several experimental methods for detemiming the AG s of chemical reactions, one can start to organize the infomiation in a systematic way. (To complete this satisfactorily, or at least efficiently and precisely, one... [Pg.366]

The NMR experimental methods for studying chemical exchange are all fairly routine experiments, used in many other NMR contexts. To interpret these results, a numerical model of the exchange, as a frmction of rate, is fitted to the experimental data. It is therefore necessary to look at the theory behind the effects of chemical exchange. Much of the theory is developed for intennediate exchange, and this is the most complex case. However, with this theory, all of the rest of chemical exchange can be understood. [Pg.2092]

Ramsden J J 1993 Review of new experimental methods for investigating random sequential adsorption J. Stat. Phys. 73 853-77... [Pg.2846]

Ramsden J J 1994 Experimental methods for investigating protein adsorption kinetics at surfaces Q. Rev. Blophys. 27 41-105... [Pg.2848]

For both copolymers and stereoregular polymers, experimental methods for characterizing the products often involve spectroscopy. We shall see that nuclear magnetic resonance (NMR) spectra are particularly well suited for the study of tacticity. This method is also used for the analysis of copolymers. [Pg.424]

Figure 8.34 Experimental method for extended X-ray absorption fine structure (EXAFS)... Figure 8.34 Experimental method for extended X-ray absorption fine structure (EXAFS)...
Experimental methods for determining the potential of materials to produce hypersensitivity reactions by inhalation use procedures to detect hyperreactivity of the airways as demonstrated by marked changes in resistance to air flow, and the detection of antibodies in blood semm (93). [Pg.236]

The electrokinetic effect is one of the few experimental methods for estimating double-layer potentials. If two electrodes are placed in a coUoidal suspension, and a voltage is impressed across them, the particles move toward the electrode of opposite charge. For nonconducting soHd spherical particles, the equation controlling this motion is presented below, where u = velocity of particles Tf = viscosity of medium V = applied field, F/cm ... [Pg.533]

The experimental methods for producing planar shock compression can be divided into three general categories, namely, explosives, guns, and energy deposition. Guns are considered the most versatile of the three. [Pg.69]

A common experimental method for creating a region of spall is through the flat impact of plates of material. Such impact leads to a process of planar spall in which an interior planar region of material is carried into tension and failure occurs through a process of crack formation or hole cavitation. Much... [Pg.266]

Numerical simulations offer several potential advantages over experimental methods for studying dynamic material behavior. For example, simulations allow nonintrusive investigation of material response at interior points of the sample. No gauges, wires, or other instrumentation are required to extract the information on the state of the material. The response at any of the discrete points in a numerical simulation can be monitored throughout the calculation simply by recording the material state at each time step of the calculation. Arbitrarily fine resolution in space and time is possible, limited only by the availability of computer memory and time. [Pg.323]

J. P. Holman. Experimental Methods for Engineers. New York McGraw-Hill, 1994. [Pg.1175]

As the titration begins, mostly HAc is present, plus some H and Ac in amounts that can be calculated (see the Example on page 45). Addition of a solution of NaOH allows hydroxide ions to neutralize any H present. Note that reaction (2) as written is strongly favored its apparent equilibrium constant is greater than lO As H is neutralized, more HAc dissociates to H and Ac. As further NaOH is added, the pH gradually increases as Ac accumulates at the expense of diminishing HAc and the neutralization of H. At the point where half of the HAc has been neutralized, that is, where 0.5 equivalent of OH has been added, the concentrations of HAc and Ac are equal and pH = pV, for HAc. Thus, we have an experimental method for determining the pV, values of weak electrolytes. These p V, values lie at the midpoint of their respective titration curves. After all of the acid has been neutralized (that is, when one equivalent of base has been added), the pH rises exponentially. [Pg.48]

The classical representation of a homopolymer chain, in which the end groups are disregarded and only one monomer residue is considered, allows no possibility for structural variation. However, possibilities for stercoscqucnce isomerism arise as soon as the monomer residue is considered in relation to its neighbors and the substituents X and Y are different. The chains have tacticity (Section 4,2.1). Experimental methods for tacticity determination are summarized in 4.2.2 and the tacticity of some common polymers is considered in 4.2.3. [Pg.168]

Although R2 is the easiest quantity to be obtained theoretically, there is no straigthforward experimental method for its determination. For this reason, two other quantities are widely in use to characterize the dimensions of a randomly coiled polymer molecule ... [Pg.80]

Experimental methods for studying solid—solid interactions... [Pg.37]

It should be emphasized that whereas the theoretical modelling of An3+ spectra in the condensed phase has reached a high degree of sophistication, the type of modelling of electronic structure of the (IV) and higher-valent actinides discussed here is restricted to very basic interactions and is in an initial state of development. The use of independent experimental methods for establishing the symmetry character of observed transitions is essential to further theoretical interpretation just as it was in the trivalent ion case. [Pg.196]

Equations (11) and (12) provide two experimental methods for evaluation K A.. (ss). Experimental agreement confirms the accuracy 85 the population density distribution obtained by GPC. [Pg.378]

Table 6.1 Experimental methods for determining different types of average relative molar mass of polymers... Table 6.1 Experimental methods for determining different types of average relative molar mass of polymers...
J. -P., Warna, )., Maki-Arvela, P., Toukoniitty, E., and Toppinen, S. (2004) Advanced kinetic concepts and experimental methods for catalytic three-phase processes. Ind. Eng. Chem. Res., 43, 4540-4550. [Pg.187]

For further discussion of experimental methods for determination of electrophoretic titration curves of proteins, see the recent study by Gianazza et al. [129], For discussion of the free solution mobility of DNA see Stellwagen et al. [368],... [Pg.589]

The most popular, and also a very accurate, experimental method for measuring nonselective spin-lattice relaxation-rates is the inversion recovery (180°-r-90°-AT-PD)NT pulse sequence. Here, t is the variable parameter, the little t between pulses, AT is the acquisition time, PD is the pulse delay, set such that AT-I- PD s 5 x T, and NT is the total number of transients required for an acceptable signal-to-noise ratio. Sequential application of a series of two-pulse sequences, each using a different pulsespacing, t, gives a series of partially relaxed spectra. Values of Rj can... [Pg.138]

To determine a chemical formula, we would like to count the atoms of each element in one molecule of the compound. Atoms are too small to count, but we might hope to measure the number of moles of each element present in one mole of the compound. Unfortunately, there is no direct experimental method for measuring moles. Instead, laboratory experiments give the masses of the various elements contained in some total mass of the compound. [Pg.155]

We return to the relationship between rate laws and mechanisms in Section 15-1. after discussing experimental methods for determining the rate law of a reaction. [Pg.1063]

The Volta potential is defined as the difference between the electrostatic outer potentials of two condensed phases in equilibrium. The measurement of this and related quantities is performed using a system of voltaic cells. This technique, which in some applications is called the surface potential method, is one of the oldest but still frequently used experimental methods for studying phenomena at electrified solid and hquid surfaces and interfaces. The difficulty with the method, which in fact is common to most electrochemical methods, is lack of molecular specificity. However, combined with modem surface-sensitive methods such as spectroscopy, it can provide important physicochemical information. Even without such complementary molecular information, the voltaic cell method is still the source of much basic electrochemical data. [Pg.13]


See other pages where Experimental methods for is mentioned: [Pg.2580]    [Pg.2747]    [Pg.657]    [Pg.131]    [Pg.238]    [Pg.453]    [Pg.30]    [Pg.198]    [Pg.203]    [Pg.2]    [Pg.202]    [Pg.442]    [Pg.173]    [Pg.575]    [Pg.594]    [Pg.598]    [Pg.397]    [Pg.1453]    [Pg.256]   
See also in sourсe #XX -- [ Pg.138 , Pg.139 , Pg.140 , Pg.141 ]




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Appendix Experimental Methods for In-situ Investigations

Development of experimental methods for determining the phase separation region, critical point, spinodal and interaction parameter

Experimental Design Chart for Block-Between Method

Experimental Methods for Bulk Measurements

Experimental Methods for Complete Kinetic Analysis

Experimental Methods for Determining Mixing Quality and Residence Time Distribution

Experimental Methods for Determining Rate Laws

Experimental Methods for Determining Virial Coefficients

Experimental Methods for Finding Rates

Experimental Methods for Hard Viscoelastic Solids

Experimental Methods for Investigating Fuel Cell Stacks

Experimental Methods for Measurement of Particle-Surface Adhesion

Experimental Methods for Parameter Estimations

Experimental Methods for Polyethylene Research Program

Experimental Methods for Shear Measurements

Experimental Methods for Soft Viscoelastic Solids and Liquids of High Viscosity

Experimental Methods for Study of Foam and Antifoam Action

Experimental Methods for Studying Phase Behaviour of Mixtures at High Temperatures and Pressures

Experimental Methods for the Determination of Transition Probabilities

Experimental method and apparatus for alumina dissolution rate measurement

Experimental methods for assessment of emulsion stability

Experimental methods for determining

Experimental methods for isothermal calorimetric reaction data

Experimental methods for isothermal infrared reaction data

Experimental methods for measuring BDEs

Experimental methods for scale-up

Experimental methods for study

Experimental methods for the determination of coke formation and

Method for experimental measurement of particles residence time distribution

Practical experimental methods for whole-cell biotransformations using bacteria and fungi

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