Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Current, concentration

These multidimensional analyses do not necessarily predict overall generator performance or operating characteristics significantly more accurately than do the qua si-one-dimensional analyses, which are more economical to mn. Thus the latter are used for general channel design calculations, and the more sophisticated codes mainly to deal with more detailed aspects of channel operation. For example, current concentrations at electrode edges can be predicted by use of the more sophisticated codes. This allows appropriate electrode design for the condition. [Pg.418]

The main cause of anode wear is electrochemical oxidation or sulfur attack of anodic surfaces. As copper is not sufficiently resistant to this type of attack, thin caps of oxidation and sulfur-resistant material, such as platinum, are bra2ed to the surface, as shown in Eigure 15a. The thick platinum reinforcement at the upstream corner protects against excessive erosion where Hall effect-induced current concentrations occur, and the interelectrode cap protects the upstream edge from anodic corrosion caused by interelectrode current leakage. The tungsten undedayment protects the copper substrate in case the platinum cladding fails. [Pg.429]

A simple electrochemical flow-through cell with powder carbon as cathodic material was used and optimized. The influence of the generation current, concentration of the catholyte, carrier stream, flow rate of the sample and interferences by other metals on the generation of hydrogen arsenide were studied. This system requires only a small sample volume and is very easily automatized. The electrochemical HG technique combined with AAS is a well-established method for achieving the required high sensitivity and low detection limits. [Pg.135]

In the technological approach, qualitative and quantitative inforraatioii on emissions released by various production and work processes, as well as data on control technology performance, are required in order to specify the air quality target levels that are technically and economically feasible. The approach is based on information on current concentration levels that are achieved by different control technologies, ranging from standard practices to the most advanced technology options (Fig. 6.7). [Pg.399]

A preliminary proposal, ba.sed on the fact that 5% of the current concentrations of formaldehyde are equal to or below this level. [Pg.403]

In this step, the assessor qiuuitifies tlie magnitude, frequency and duration of exposure for each patliway identified in Step 2. Tliis step is most often conducted in two stages estimation of exposure concentrations and calculation of intakes. The later estimation is considered in Step 4. In tliis part of step 3. the exposure assessor determines the concentration of chemicals tliat will be contacted over the exposure period. E.xposure concentrations are estimated using monitoring data and/or chemical transport and environmental fate models. Modeling may be used to estimate future chemical concentrations in media tliat are currently contaminated or tliat may become contaminated, and current concentrations in media and/or at locations for which tliere are no monitoring data. The bulk of the material in tliis chapter is concerned witli tliis step. [Pg.356]

When corrosion of a chromium-coated metal takes place, the corroding current concentrates its action on fissures in the deposit. There appears to be an incubation period, after which rapid attack occurs in the form of pits, and... [Pg.549]

Computer projections of atmospheric CC2 concentration for the next 200 years predict escalating increases in C02 concentration. Only about half the C02 released by humans is absorbed by Earth s natural systems. The other half increases the C02 concentration in the atmosphere by about 1.5 ppmv per year. Two conclusions can be drawn from the these facts. First, even if C02 emissions were reduced to the amount emitted in 1990 and held constant at that level, the concentration of CO, in the atmosphere would continue to increase at about 1.5 ppmv per year for the next century. Second, to maintain C02 at its current concentration of 360 ppmv, we would have to reduce fossil fuel consumption by about 50% immediately. [Pg.731]

The addition of an hydroperoxide-breaking substance S to oxidized RH decreases the current concentration of ROOH. This cannot affect the rate of oxidation if the radicals are produced by radiant energy or other sources unreactive to S, but it slows down the oxidation if radicals are produced from hydroperoxide. The initial step of oxidation in the absence of a peroxy-trapping substance is described by the equation (see Chapter 4)... [Pg.620]

Of the 30 lakes that were cored 9 reached geochemical background concentrations and had current concentrations and/or fluxes that are decreasing to present. Five additional lakes that did not reach geochemical background were included for comparison to current wet deposition. Linear models of recovery were estimated on the most recent decreasing trend of concentration and/or flux and by ignoring episodic or short term increases in fluxes or concentrations (Fig. 1). [Pg.268]

Current concentrations of GHG have already caused the mean global temperature to increase by 0.76 °C in the period from 1850 to 2005 owing to the inertia of the climate system this will lead to at least a further half-degree warming over the next few decades. Eleven of the twelve years from 1995 to 2006 rank among the 12 warmest years in the instrumental record of global surface temperature (since 1850). [Pg.17]

Based on the optimization criterion, SpinPro can select the most appropriate rotor. For example, suppose the investigator has a relatively large sample volume, all of which needs to be processed as soon as possible. The "minimize cumulative run time" criterion would be the appropriate choice. SpinPro would then initiate the following rotor selection procedure SpinPro determines the total sample volume based on inputs of the sample volume, the current concentration of the sample, and a correction for any pre-run dilutions of the sample. Next, consideration is made for whether tubes or bottles will be used. The program then evaluates rotors for the number of tube positions and the amount of sample per tube. At this point, SpinPro will have estimated for each rotor the number of runs required to process the sample. SpinPro then estimates the run time for each rotor to perform a single run. Based on these estimates, SpinPro selects the rotor that will give the shortest total run time when the run time is summed over the total number of runs. Similarly, the investigator can select any of the optimization criteria and initiate a variety of precise rotor selection procedures. [Pg.300]

Typically, k 1 A. For R 1000 A, at Ax 45 A, the current drops by a factor of that is, about one order of magnitude. For / 100 A, the current concentrates in a small circle of radius 14 A. Therefore, with moderate means, a very high lateral resolution is expected. [Pg.9]

Interpolation in the internal NOEC-SSD confirmed that the current concentrations still are above safe levels (Figure 5). In the study of Ross et al. (2002), harbour seals with 209 ng TEQ/g Iw were reported to reveal significantly more immunotoxic effects than the reference seals containing 62 pg TEQ/g Iw. It would be useful to study specific dioxin-related biomarker responses... [Pg.110]

We start our discussion of specific reaction rate laws by examining the results of a simple experiment in which we observe how the concentration of benzyl chloride (Fig. 12.1) changes as a function of time in aqueous solutions of pH 3, 6, and 9 at 25°C (Fig. 12.2). When plotting the concentration of benzyl chloride (denoted as [A]) as a function of time, we find that we get an exponential decrease in concentration independent of pH (Fig. 12.2a). Hence, we find that the turnover rate of benzyl chloride is always proportional to its current concentration. This can be expressed mathematically by a first-order rate law ... [Pg.469]

Statement 2. Substitution into the concentration dynamics (equations (8.2.12) and (8.2.13)) of the reaction rate K — K(Na, Nb), dependent on the current concentrations, changes the nature of the singular point. In particular, a centre (neutral stability) could be replaced by stable or unstable focus. This conclusion comes easily from the topological analysis its illustrations are well-developed in biophysics (see, e.g., a book by Bazikin [30]). [Pg.482]

Therefore, oscillations of K (t) result in the transition of the concentration motion from one stable trajectory into another, having also another oscillation period. That is, the concentration dynamics in the Lotka-Volterra model acts as a noise. Since along with the particular time dependence K — K(t) related to the standing wave regime, it depends also effectively on the current concentrations (which introduces the damping into the concentration motion), the concentration passages from one trajectory onto another have the deterministic character. It results in the limited amplitudes of concentration oscillations. The phase portrait demonstrates existence of the distinctive range of the allowed periods of the concentration oscillations. [Pg.487]

For a given set of parameters the period of concentration oscillations (or its average for a periodic motion) exceeds greatly the period of the correlation motion. For the slow concentration motion not only the period of the standing wave oscillations but also their amplitudes and, consequently, the amplitude in the K (t) oscillations depend on the current concentrations Na(t) and Nb(t). In other words, the oscillations of the reaction rate are modulated by the concentration motion. Respectively, the influence of the time dependence K K(t) upon the concentration dynamics has irregular, aperiodic character. A noise component modulates the autowave component (the standing waves) but the latter, in its turn, due to back-coupling causes transition to new noise trajectories. What we get as a result is aperiodic motion (chaos). The mutual influence of the concentration and correlation motions and vice versa is illustrated in Fig. 8.2, where time developments of both the concentrations and reaction rates are plotted. [Pg.487]

Finally, Pittinger and Kimerle (62) calculated hypothetical water-quality criteria for C12LAS. The values calculated are 0.23 mg/L for continuous concentration and 0.625 mg/L for maximum concentration. Therefore, laboratory and field data confirm that current concentrations of C12LAS in the aquatic environment are safe. [Pg.547]

Here, D is the diffusion coefficient of the reacting particles and n(t) and N(t) are the current concentrations of the two reagents. The solution of the system of equations (46) is written in the form of a complex series (see, for example, ref. 27). However, it is substantially simplified in two practically important limits t td and t > td, where td = a2/D is the time of diffusion travel of the reagents at a distance of the order of a. For the sake of simplicity we shall consider only the case of random spatial distribution of the reagents and assume that n(0) N. If t tu, then the solution of eqns. (46) is given by expression (35), i.e. it coincides with the equation for the kinetics of electron tunneling reactions for immobile reagents. At t > tu, from eqn. (46) it is possible to obtain... [Pg.133]

Here, n(t)/n(t0) is the ratio of the current concentration, n(t), of the reagent present in the smaller amount (in this case S04") to its concentration at a certain fixed time moment, tof N is the concentration of the second reagent, and p = ndlj2) xvz vvtQ. In accordance with eqn. (1), the observed kinetics of S04 decay presents straight lines in the coordinates of Fig. 1. [Pg.226]

The activation energy of the decay of P700+ in the range 80-160 K was found from the data of Fig. 8 using eqn. (5). For the ratio of the current concentration of pairs, n(t)> to their concentration at time 0 one can readily obtain from eqn. (5), by analogy with eqn. (9) of Chap. 3... [Pg.286]

The following chapter describes the changes in concentration of POPs in ambient air in Europe through time, with a focus on current concentrations. It also... [Pg.75]

None of the technologies listed in Table 1.1 can alone provide a short- to medium-term solution to reduce atmospheric C02 emissions at a level necessary to stabilize current concentrations. Rather, the correct blend of technologies... [Pg.5]


See other pages where Current, concentration is mentioned: [Pg.379]    [Pg.222]    [Pg.402]    [Pg.7]    [Pg.287]    [Pg.288]    [Pg.232]    [Pg.169]    [Pg.94]    [Pg.173]    [Pg.708]    [Pg.424]    [Pg.630]    [Pg.1940]    [Pg.124]    [Pg.295]    [Pg.165]    [Pg.133]    [Pg.174]    [Pg.108]    [Pg.485]    [Pg.53]    [Pg.148]    [Pg.172]    [Pg.864]    [Pg.72]   
See also in sourсe #XX -- [ Pg.86 ]




SEARCH



Catalytic Currents buffer concentration

Catalytic Currents concentration

Concentration influence current density

Concentration polarization current density calculation

Concentration-Time Dependence at Constant Current (Galvanostatic Regime)

Current-concentration relationships, potential

Current-concentration relationships, potential voltammetry

Electrorefining of Metals. Concentration Polarization and the Limiting Current Density

Exchange current density concentration dependence

Near-bottom currents and oxygen concentrations

Total corrosion current, water concentration

© 2024 chempedia.info