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Zero curve

Discounted cash-flow rate of return. Discounted cash-flow rate of return is defined as the discount rate i which makes the NPV of a project zero (curve 3 in Fig. A.2) ... [Pg.424]

After a few voltage cycles, the shape of the curve changes, and finally the zero curve", shown dotted in the figure, is obtained. The areas under the anodic and cathodic peaks are here equal and correspond to the transfer of one electron per TAA molecule. We assume that these reproducible peaks, whose position is independent of the pH of the electrolyte, are caused by a change in valency of the central cobalt atom. [Pg.167]

The CoTAA catalysts obtained by the three activation methods show different electrochemical behavior. This appears particularly clearly in the triangular voltage diagrams obtained under inert gas. The curve for chemically activated CoTAA (Fig. 27) is similar to the constant zero curve of electrochemically activated... [Pg.169]

Equation (3.17) allows a different interpretation of the underlying system s bifurcation behavior by taking Kc and yc as fixed and letting a vary, for example. We now study the bifurcation behavior of nonadiabatic and nonisothermal CSTR systems via their level-zero curves for the associated transcendental surface z = g(a,y). The surface is defined as before, except that here we treat Kc and yc as constants and vary a and y in the 3D surface equation... [Pg.102]

Under potentiostatic conditions, the electrode potential is set on the plateau of the A —> B transition. During the electrolysis, the current will decrease with the concentration of A and reach zero (curve d). The process is quite selective, as the other electrode process cannot take place. Note that this electro synthetic procedure requires the use of a potentiostat with three electrodes (working, reference, and auxiliary). [Pg.762]

Figure 6.5.2 Cyclic voltammograms under the same conditions as in Figure 6.5.1, but in an i-E format. E of (1) E1/2 — 90/n (2) E1/2 — 130/n (3) Ey2 - 200/n mV (4) for potential held at E 4 until the cathodic current decays to zero. [Curve 4 results from reflection of the cathodic i-E curve through the E axis and then through the vertical line at n E — F1/2) = 0. Curves 1, 2, and 3 result by addition of this curve to the decaying current of the cathodic i-E curve (1, 2, or 3 )-]... Figure 6.5.2 Cyclic voltammograms under the same conditions as in Figure 6.5.1, but in an i-E format. E of (1) E1/2 — 90/n (2) E1/2 — 130/n (3) Ey2 - 200/n mV (4) for potential held at E 4 until the cathodic current decays to zero. [Curve 4 results from reflection of the cathodic i-E curve through the E axis and then through the vertical line at n E — F1/2) = 0. Curves 1, 2, and 3 result by addition of this curve to the decaying current of the cathodic i-E curve (1, 2, or 3 )-]...
Figure 13. Scheme of peak-fading process and formation of the 7r-state of DNA, recorded by a.c. polarography. Curve 0 base electrolyte Curve 1 peak 0 and of ds-DNA, 65°C Curve 2 decrease of peak 0, fixed potential Curve 3 rest peak 0 at more positive potential, and Curve 4 its decrease to zero Curve 5 adsorption region of the 7r-state of DNA Curve 6 anodic polarization—only peak 0 is recorded. [Pg.208]

EXHIB[T20.3 EUR Swap Zero Curve (Continuously Compounded) as of 14 April 2000... [Pg.645]

EXHIB[T20.7A Linear Interpolation Swap Zero Curve by Currency (continuously compounded)... [Pg.649]

This pertains to parts in service such as fasteners, seals, or screws. An example of results of such a test are shown in Fig. 24.8. The relaxing stress could conceivably fall to zero (curve a in the bottom part of Fig. 24.8) but in practice the behavior displayed as curve b is observed, so that a certain level of internal stress [Pg.432]

Chart of the nuclides. Black squares show stable nuclides as a function of atomic number Z and neutron number N. Sp zero and Sn zero curves indicate proton and neutron drip lines, respectively, which can be predicted, e.g., from different mass formulae. The 6/rcurves show limits, where the potential barrier disappears for fission. Grey regions indicate the domain of known nuclides. Magic numbers are shown by horizontal and vertical lines... [Pg.62]

The completion of the wash-out operations should be checked as carefully as the chemical transformations on polymer, since remaining by-products would cause side reactions in subsequent steps of the synthesis. In our group, this is simply and sensitively performed by the continuously monitoring control system, which operates during the whole Merrifield synthesis. On the recordings, completed wash-out operations after each chemical reaction on polymer are indicated by a straight zero curve, since reference and sample flow cell of the photometric unit in this situation contain nothing but pure solvent. [Pg.62]

Fig.ir.3-12 Schematic representation of high-penneability regions in the ternary system Ni—Fe—Me by means of the zero curves Ki, kioo — 0 and Am = 0 for additives with valence I-VIII [3.15]... [Pg.771]

Our starting point is a set of zero curve tenors (or discount factors) obtained from a collection of market instruments such as cash deposits, futures, swaps, or coupon bonds. We therefore have a set of tenor points and their respective zero rates (or discount factors). The mathematics of cubic splines is straightforward, but we assume a basic understanding of calculus and a familiarity with solving simultaneous linear equations by substitution. An account of the methods analyzed in this section is given in Burden and Faires (1997), which has very accessible text on cubic spline interpolation. ... [Pg.97]

We assume that the practitioner has already calculated a set of nodes using a yield curve construction technique such as bootstrapping. A zero curve is then fitted using the cubic spline methodology by interpolating between nodes using individual cubic polynomials. Each polynomial has its own parameters but is constructed in such a way that its ends touch each node at the start and end. The set of splines, which touch at the nodes, therefore form a continuous curve. Our objective is to... [Pg.97]

Using the actual United Kingdom 10-year zero curve for January 2, 2000, the forward rates have been calculated using cubic spline and linear interpolation and compared in FIGURE 5.15 and FIGURE 5.16 respectively. There is no observed reason to favor the latter approach over the former. [Pg.115]

We have presented an accessible account of how the cubic spline methodology of term structure estimation could be implemented by users involved in any area of the debt capital markets. The technique is straightforward and quick, and is valid for a number of applications, most of which are normal or conventional yield curves. For example, users are recommended to use it when curves are positively sloping, or when the long end of the curve is not downward sloping. The existence of humps along the short or medium terms of the curve can cause excessive oscillation in the forward curve, but the zero curve may still be used for valuation or relative value purposes. [Pg.119]

Oscillation is a natural effect of the cubic spline methodology, and its existence does not impair its effectiveness under many conditions. If observed rates produce very humped curves, the fitted zero-curve using cubic spline does not produce usable results. For policy-making purposes, for example, as used in central banks, and also for certain market valuation purposes, users require forward rates with minimal oscillation. In such cases, however, the Waggoner or Anderson—Sleath models will overcome this problem. We therefore recommend the cubic spline approach under most market conditions. [Pg.119]

Like catalytic hydrogen evolution, catalytic proton transfer may have surface or volume characteristics, i.e., the transfer may occur onto a compound adsorbed at the electrode or onto a depolarizer in the vicinity of the electrode. If small amounts of the strongly adsorbed polyvinyl alcohol are added to the solution, at the moment when the electrode surface is completely covered with this compound the surface kinetic reduction current of protonated propiophenone decreases almost to zero (Curves 1, Fig. 27). If pyridine catalyst is added to the solution, reduction current for the protonated propiophenone is also observed on the completely covered electrode surface (Curves 2-4, Fig. 27), and even a considerable increase in the... [Pg.128]


See other pages where Zero curve is mentioned: [Pg.649]    [Pg.88]    [Pg.726]    [Pg.140]    [Pg.82]    [Pg.89]    [Pg.274]    [Pg.392]    [Pg.39]    [Pg.448]    [Pg.140]    [Pg.285]    [Pg.75]    [Pg.143]    [Pg.616]   
See also in sourсe #XX -- [ Pg.821 ]




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