Constant retarding ratio

In most electron spectroscopic analyses, the kinetic energies of the electrons entering the analyzer are retarded to either a constant energy or by a constant factor. These approaches lead to two modes of operation the constant analyzer energy (CAE) mode and the constant retard ratio (CRR) mode. 

There are two operating modes known as Constant Retard Ratio (CRR) or Constant Analysis Energy (CAE). In CRR, the electrons are slowed down by an amount which is a constant ratio of the electron energy to be analysed. For example, if the retard ratio is 10 and 1000 eV electrons are to be detected, then the electrons will be slowed down to 100 eV and the pass energy will be set to 100 eV. In CAE, the pass energy is fixed. If the pass energy is 50 eV, then electrons of 1000 eV will have to be slowed down by 950 eV in order to be detected. 

Constant conduction heat pipes, 13 227 Constant failure rate, 13 167 Constant-field scaling, of FETs, 22 253, 254 Constant-modulus alloys, 17 101 Constant of proportionality, 14 237 Constant pressure heat capacity, 24 656 Constant rate drying, 9 103-105 Constant rate period, 9 97 23 66-67 Constant retard ratio (CRR) mode, 24 103 Constant slope condition, 24 136-137 Constant stress test, 13 472 19 583 Constant-voltage scaling, of FETs, 22 253 Constant volume heat capacity, 24 656 Constant volume sampling system (CVS), 10 33... 

The combination of retardation and deflection allows two different modes of operation. In the constant analyzer energy (CAE) mode the pass energy is kept constant and the spectrum is scanned by a variation of the retarding field. In this mode the resolution AEa is kept constant over the whole spectrum. In the constant retard ratio mode (CRR) the voltage difference between the hemispheres is proportional to the retarding field. In this mode the relative resolution AEjE is kept constant. The CAE mode is normally used for PES, the CRR mode for Auger spectroscopy. 

The electron energy selection is usually made through two different modes fixed analyzer transmission and fixed retardation ratio. The first one is the one used when a quantitative analysis is required. It consists of keeping the analyzer voltages constant, the kinetic energy being swept by a variable retardation voltage... 

The CRR mode involves retarding the electron kinetic energies to a constant ratio of H /H where H is the energy passed by the analyzer. Thus, the energies are retarded by a constant factor. Spectra acquired in this mode ate less easy to quantify, but small peaks at low kinetic energies ate readily detected. This mode of operation results in spectra of constant relative resolution throughout. The relative resolution is improved in this mode by a factor of E. ... 

In studies of the polymerization kinetics of triaUyl citrate [6299-73-6] the cyclization constant was found to be intermediate between that of diaUyl succinate and DAP (86). Copolymerization reactivity ratios with vinyl monomers have been reported (87). At 60°C with benzoyl peroxide as initiator, triaUyl citrate retards polymerization of styrene, acrylonitrile, vinyl choloride, and vinyl acetate. Properties of polyfunctional aUyl esters are given in Table 7 some of these esters have sharp odors and cause skin irritation. 

The effectiveness of inhibitors is measured in terms of the rate constant ratio kz/kp and the stoichiometric coefficient. The stoichiometric coefficient is the moles of radicals consumed per mole of inhibitor. These parameters may be determined by various methods. A brief description of the classical kinetic treatment for evaluating k7/kp follows. Consider the reaction scheme shown which describes ideal inhibition and retardation (Scheme 5.11). 

The reduction of iodine by ferrocyanide is simple second-order with Aij (25 °C) = (1.3 + 0.3)x 10 l.mole sec This is the reverse of the oxidation of iodide by ferricyanide (p. 409), but the ratio k(forward)/k(back) does not agree well with the equilibrium constant determined potentiometrically. Addition of 1 strongly retards the reduction and 13 was discounted as a reactant, the mechanism suggested being... 

As noted above, the duration of the retarding action of an inhibitor is directly proportional to the / value. In systems with a cyclic chain termination mechanism, the / coefficient depends on the ratio of the rate constants for two reactions, in which the inhibitor is regenerated and irreversibly consumed. In the oxidation of alcohols, aminyl radicals are consumed irreversibly via the reaction with nitroxyl radical formation (see earlier) and via the following reaction [11] ... 

The level of impurity uptake can be considered to depend on the thermodynamics of the system as well as on the kinetics of crystal growth and incorporation of units in the growing crystal. The kinetics are mainly affected by the residence time which determines the supersaturation, by the stoichiometry (calcium over sulfate concentration ratio) and by growth retarding impurities. The thermodynamics are related to activity coefficients in the solution and the solid phase, complexation constants, solubility products and dimensions of the foreign ions compared to those of the ions of the host lattice [2,3,4]. 

The application of force to a stationary or moving system can be described in static, kinematic, or dynamic terms that define the mechanical similarity of processing equipment and the solids or liquids within their confines. Static similarity relates the deformation under constant stress of one body or structure to that of another it exists when geometric similarity is maintained even as elastic or plastic deformation of stressed structural components occurs [53], In contrast, kinematic similarity encompasses the additional dimension of time, while dynamic similarity involves the forces (e.g., pressure, gravitational, centrifugal) that accelerate or retard moving masses in dynamic systems. The inclusion of tune as another dimension necessitates the consideration of corresponding times, t and t, for which the time scale ratio t, defined as t = t It, is a constant. 

Total S content cannot indicate whether increased carbon inputs to sediments cause increased diffusion of sulfate into sediments or restrict reoxidation and release of S from sediments, because the net effect is the same. In a survey of 14 lakes, Rudd et al. (80) did not observe a strong correlation between organic matter content per volume and net diffusive flux of sulfate. However, in English lakes the lowest C S ratios occur in the most productive lakes (24) whether this represents enhanced influx or retarded release is not clear. Among 11 Swiss lakes, ratios of C to S sedimentation rates are relatively constant and substantially below C S ratios in seston net S fluxes... 

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