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Enzymes are classified in terms of the reactions which they catalyse and were formerly named by adding the suffix ase to the substrate or to the process of the reaction. In order to clarify the confusing nomenclature a system has been developed by the International Union of Biochemistry and the International Union of Pure and Applied Chemistry (see Enzyme Nomenclature , Elsevier, 1973). The enzymes are classified into divisions based on the type of reaction catalysed and the particular substrate. The suffix ase is retained and recommended trivial names and systematic names for classification are usually given when quoting a particular enzyme. Any one particular enzyme has a specific code number based upon the new classification. [Pg.159]

The same definition of viscosity applies to oil as gas (see Section 5.2.6), but sometimes the kinematic viscosity is quoted. This is the viscosity divided by the density (u = i7p), and has a straight line relationship with temperature. [Pg.109]

Oil density at surface conditions is commonly quoted in API, as discussed in Section 5.2.3. [Pg.109]

Caution is required in the use of the simple cashflow indicators, since they fail to take account of changing general price levels or the cost of capital (discussed in Section 13.4). It is always recommended that the definition of the indicators is quoted for clarity of understanding. [Pg.317]

What we have calculated is the present value (at a particular reference date) of a future sum of money, using a specified discount rate. In any discounting calculation, it is important to quote the reference date and the discount rate. [Pg.319]

In this article, we are contented to quote only the theoretical principle, the development and the implantation will make the object of future works. [Pg.226]

The ultrasonic images that we want to process are HF- type, (i.e., huilt from High Frequency signals. Fig. 4). Consequently, the noise is situated in the eentral part of the matrix. In order that we define two thresholds tl and t2. These last will be determined by using one of some measures quoted in the bibliography. [Pg.235]

It is clear that, apart from the production regime, other factors may influence the freight values obtained (film type, regeneration quotes, electrolysis unit,. ..). In case of G335SF in combination with STRUCTURIX SILVERFIX, which has a maximum current of 3A and a typical response of 4 A.l/g, I5m of film per day is judged to be the maximum production to meet silver freights below 50 mg/m. ... [Pg.608]

Landau L D 1935 quoted in Landau L D and Lifshitz E M 1958 Stetisticel Physics oh XIV, section 135 (Oxford Pergamon)... [Pg.556]

We will quote a numerical constant in some of these equations to help with actual calculations. The units can be very confusing because it is conventional to use non-SI units for several quantities. The wavenumber value, i>, is usually taken to be in cm The extinction coefficient is conveniently taken in units of 1 moH ... [Pg.1126]

Unfortimately for modem crystallographers, all of tlie crystal stmctiires that could be solved by the choose-the-best-of-a-small-niunber-of-possibilities procedure had been solved by 1920. Bragg has been quoted as saying that the pyrite stmcture was very complicated , but he wrote, in about 1930, It must be realized, however, that (cases having one or two parameters) are still extremely simple. The more typical crystal may have ten, twenty, or forty parameters, to all of which values must be assigned before the analysis of the stmcture is complete. This statement is read with amusement by a modem crystallographer, who routinely works with hundreds and frequently with thousands of parameters. [Pg.1373]

Figure Bl.11.1. Resonance frequencies for different nuclei in a field of 14.1 T. Widths indicate the quoted range of shifts for each nucleus, and heights mdicate relative sensitivities at the natural isotopic abundance, on a log scale covering approximately six orders of magnitude. Nuclei resonatmg below 140 MHz are not shown. Figure Bl.11.1. Resonance frequencies for different nuclei in a field of 14.1 T. Widths indicate the quoted range of shifts for each nucleus, and heights mdicate relative sensitivities at the natural isotopic abundance, on a log scale covering approximately six orders of magnitude. Nuclei resonatmg below 140 MHz are not shown.
Because J arises from the magnetic interactions of nuclei, the simplest factor affecting it is the product yjY of the two nuclear magnetogyric ratios involved. For example, in FI F is 82 FIz, i.e. x yo/yf - This totally predictable factor is sometimes discounted by quoting the reduced coupling constant =... [Pg.1452]

If the molecules could be detected with 100% efficiency, the fluxes quoted above would lead to impressive detected signal levels. The first generation of reactive scattering experiments concentrated on reactions of alkali atoms, since surface ionization on a hot-wire detector is extremely efficient. Such detectors have been superseded by the universal mass spectrometer detector. For electron-bombardment ionization, the rate of fonnation of the molecular ions can be written as... [Pg.2062]

In the theory of the liquid state, the hard-sphere model plays an important role. For hard spheres, the pair interaction potential V r) = qo for r < J, where d is the particle diameter, whereas V(r) = 0 for r s d. The stmcture of a simple fluid, such as argon, is very similar to that of a hard-sphere fluid. Hard-sphere atoms do, of course, not exist. Certain model colloids, however, come very close to hard-sphere behaviour. These systems have been studied in much detail and some results will be quoted below. [Pg.2668]

A somewhat different viewpoint motivates this chapter, which stiesses the added meaning that the complex nature of the wave function lends to our understanding. Though it is only recently that this aspect has come to the forefront, the essential point was affimied already in 1972 by Wigner [5] in his famous essay on the role of mathematics in physics. We quote from this here at some length ... [Pg.95]

Section IB presents results that the analytic properties of the wave function as a function of time t imply and summarizes previous publications of the authors and of their collaborators [29-38]. While the earlier quote from Wigner has prepared us to expect some general insight from the analytic behavior of the wave function, the equations in this secbon yield the specific result that, due to the analytic properties of the logarithm of wave function amplitudes, certain forms of phase changes lead immediately to the logical necessity of enlarging... [Pg.96]

For the Berry phase, we shall quote a definition given in [164] ""The phase that can be acquired by a state moving adiabatically (slowly) around a closed path in the parameter space of the system. There is a further, somewhat more general phase, that appears in any cyclic motion, not necessarily slow in the Hilbert space, which is the Aharonov-Anandan phase [10]. Other developments and applications are abundant. An interim summai was published in 1990 [78]. A further, more up-to-date summary, especially on progress in experimental developments, is much needed. (In Section IV we list some publications that report on the experimental determinations of the Berry phase.) Regarding theoretical advances, we note (in a somewhat subjective and selective mode) some clarifications regarding parallel transport, e.g., [165], This paper discusses the projective Hilbert space and its metric (the Fubini-Study metric). The projective Hilbert space arises from the Hilbert space of the electronic manifold by the removal of the overall phase and is therefore a central geometrical concept in any treatment of the component phases, such as this chapter. [Pg.105]

The authors are indebted to Professor Michael Baer for many years of exciting collaboration, to Dr. B. Halperin for advice, to F rofessor Mark Pere lmanfor discussion and permission to quote from his preprint Temporal Magnitudes and Functions of Scattering Theory, to Professor Shmuel Elitzur for suggesting the approach leading to Alternative Derivation in Section V and to Professor Tgal Talmi for an inspiration [327],... [Pg.169]

Covalent bonding, in all the cases so far quoted, produces molecules not ions, and enables us to explain the inability of the compounds formed to conduct electricity. Covalently bonded groups of atoms can, however, also be ions. When ammonia and hydrogen chloride are brought together in the gaseous state proton transfer occurs as follows ... [Pg.42]

Ionisations 2, 3 and 5 are complete ionisations so that in water HCI and HNO3 are completely ionised and H2SO4 is completely ionised as a monobasic acid. Since this is so, all these acids in water really exist as the solvated proton known as the hydrogen ion, and as far as their acid properties are concerned they are the same conjugate acid species (with different conjugate bases). Such acids are termed strong acids or more correctly strong acids in water. (In ethanol as solvent, equilibria such as 1 would be the result for all the acids quoted above.) Ionisations 4 and 6 do not proceed to completion... [Pg.85]

Values of are small for weak acids and they range very widely (Table 4.1). It is common practice to quote values as the negative logarithm to the base ten, i.e. — logjo K.. since such numbers are less cumbersome and positive when Aj < 1. The symbol for -logio is by convention "p/ fhus -logjo becomes pK,. Table 4.1 shows some typical pAg values. [Pg.86]

In an aquo-complex, loss of protons from the coordinated water molecules can occur, as with hydrated non-transition metal ions (p. 45). To prevent proton loss by aquo complexes, therefore, acid must usually be added. It is for these conditions that redox potentials in Chapter 4 are usually quoted. Thus, in acid solutions, we have... [Pg.367]

For this reaction, charcoal is a catalyst if this is omitted and hydrogen peroxide is used as the oxidant, a red aquopentammino-cobalt(lll) chloride, [Co(NH3)jH20]Cl3, is formed and treatment of this with concentrated hydrochloric acid gives the red chloro-p0itatnmino-coba. t(lll) chloride, [Co(NH3)5Cl]Cl2. In these latter two compounds, one ammonia ligand is replaced by one water molecule or one chloride ion it is a peculiarity of cobalt that these replacements are so easy and the pure products so readily isolated. In the examples quoted, the complex cobalt(III) state is easily obtained by oxidation of cobalt(II) in presence of ammonia, since... [Pg.403]


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See also in sourсe #XX -- [ Pg.174 , Pg.365 , Pg.471 , Pg.473 , Pg.476 , Pg.478 , Pg.658 ]




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