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Flow rate and concentration

Fig. 4. Hypothetical leakage curves to show effect of ionic concentration and flow rate, where the dashed line corresponds to the leakage shutdown level... Fig. 4. Hypothetical leakage curves to show effect of ionic concentration and flow rate, where the dashed line corresponds to the leakage shutdown level...
Effects of Concentrations and Flow Rates on Chromatographic Time Delay Factors... [Pg.515]

Recently, Orosz et al. [136] reviewed and critically reevaluated some of the known mechanistic studies. Detailed mathematical expressions for rate constants were presented, and these are used to derive relationships, which can then be used as guidelines in the optimization procedure of the POCL response. A model based on the time-window concept, which assumes that only a fraction of the exponential light emission curve is captured and integrated by the detector, was presented. Existing data were used to simulate the detector response for different reagent concentrations and flow rates. [Pg.147]

Reagents to carry out the alkaline oxidation of the toxins were prepared as originally described ( ) with the exception that nitric acid was used in place of acetic acid. The reagent concentrations and flow rates are shown in Table I. [Pg.201]

Substrate A and enzyme E flow ]lhrough a mixed flow reactor (V = 6 liter). From the entering and leaving concentrations and flow rate find a rate equation to represent the action of enzyme on substrate. [Pg.619]

As pointed out earlier, CVD is a steady-state, but rarely equilibrium, process. It can thus be rate-limited by either mass transport (steps 2, 4, and 7) or chemical kinetics (steps 1 and 5 also steps 3 and 6, which can be described with kinetic-like expressions). What we seek from this model is an expression for the deposition rate, or growth rate of the thin film, on the substrate. The ideal deposition expression would be derived via analysis of all possible sequential and competing reactions in the reaction mechanism. This is typically not possible, however, due to the lack of activation or adsorption energies and preexponential factors. The most practical approach is to obtain deposition rate data as a function of deposition conditions such as temperature, concentration, and flow rate and fit these to suspected rate-limiting reactions. [Pg.744]

Inhaled (volatile) anesthetics are delivered to the lungs in gas mixtures in which concentrations and flow rates are easy to measure and control. However, dose-response characteristics of volatile anesthetics are difficult to quantify. Although achievement of an anesthetic state depends on the concentration of the anesthetic in the brain (ie, at the effect site), concentrations in the brain tissue are obviously impossible to measure under clinical conditions. Furthermore, neither the lower nor the upper ends of the graded dose-response curve defining the effect on the central nervous system can be ethically determined because at very low gas concentrations awareness of pain may occur. Moreover, at high concentrations there is a high risk of severe cardiovascular and respiratory depression. Nevertheless, a useful estimate of anesthetic potency can be obtained using quantal dose-response principles for both the inhaled and intravenous anesthetics. [Pg.545]

Monitoring of the mercury concentrations and flow rate of the ambient air used in the combustion process... [Pg.180]

Mass balance measurements for 41 elements have been made around the Thomas A. Allen Steam Plant in Memphis, Tenn. For one of the three independent cyclone boilers at the plant, the concentration and flow rates of each element were determined for coal, slag tank effluent, fly ash in the precipitator inlet and outlet (collected isokinetically), and fly ash in the stack gases (collected isokinetically). Measurements by neutron activation analysis, spark source mass spectroscopy (with isotope dilution for some elements), and atomic adsorption spectroscopy yielded an approximate balance (closure to within 30% or less) for many elements. Exceptions were those elements such as mercury, which form volatile compounds. For most elements in the fly ash, the newly installed electrostatic precipitator was extremely efficient. [Pg.183]

The requirements for these applications with respect to ozone concentration and flow rate depend on the application. For the cleaning process a liquid concentration of about 5 to 20 mg L 1 is normally mentioned, for photoresist removal much higher concentrations are required (50 mg L 1 and higher). [Pg.147]

HPLC apparatus to reduce postcolumn pump pulsation and improve CL detection levels of the DCIA derivatives. The CL solution concentrations and flow rate remained the same as those previously described. A 10-/zm C8 column (250 X 4.6-mm ID) plus a guard column (30 X 4.6-mm ID) packed with 30-yttm C l8 material was used in replacement of the ECONOSPHERE column. [Pg.190]

Two factors are driving the market for precise, very-low-flow HPLC pumping systems extremely limited sample sizes in biotechnology and the electrospray and nanospray interfaces that are concentration and flow-rate dependent. It is very difficult to get precise flow and gradient formation from pumps that have a 5- to 10-/iL plunger displacement, even using 3200-step stepper motor drives. This has forced manufacturers to resurrect a very old concept from the earliest days of HPLC, the syringe pump. [Pg.191]

The propagation of pressure waves such as acoustic wave, shock wave, and Prandtl-Meyer expansion through a gas-solid suspension is a phenomenon associated primarily with the transfer of momentum although certain processes of energy transfer such as kinetic energy dissipation and heat transfer between gas and solids almost always occur. Typical applications of the pressure wave propagation include the measurements of the solids concentration and flow rate by use of acoustic devices as well as detonation combustion such as in a rocket propellant combustor or in the barrel of a gun. [Pg.259]

The PCFC technique utilizes traditional oxygen depletion calorimetry. The specimen is first heated at a constant rate of temperature rise (typically 1-5 K/s) in a pyrolyzer. The thermal decomposition products are swept from the pyrolyzer by an inert gas. The gas stream is mixed with oxygen and enters a combustor at 900°C, where the decomposition products are completely oxidized. Oxygen concentrations and flow rates of the combustion gases are used to determine the oxygen depletion involved in the combustion process, and the heat release, as well as the heat release capacity (HRC), is determined from these measurements. [Pg.652]

Figure 12.7 presents the gas- and liquid-outlet concentrations when the gas feed rate is reduced. It should be remarked that the gas turbines produce higher NO and 02 concentrations when the gas flow rate is lower. Linear relationships between concentrations and flow rate are assumed. It turns out that the most demanding conditions are around 14000Nm3/h. However, the NO concentration in the gas-outlet stream remains below the 10ppm limit (0.1 dimensionless concentration). [Pg.357]

Figure 5.4 Module-by-module concentration and flow rate changes over a single RO stage. Assumes 11% recovery per module and 98% solute rejection. Figure 5.4 Module-by-module concentration and flow rate changes over a single RO stage. Assumes 11% recovery per module and 98% solute rejection.
Laboratory tests on two-pound sampl 5 of green petroleum cokes with sulfur contents of 4 wt% to 6 wt% have successfully reduced the sulfur levels to as low as 0.7 wt%. The degree of desulfurization can readily be controlled by adjusting the temperature (nominally between 2500 and 2800°F), the holding time in the reactor (between 5 and 90 minutes), and the reactant concentrations and flow rates. [Pg.204]

To elucidate the significance of the accuracy of concentration and flow rate measurements, two ideal situations in the reactor which are usually assumed to occur in the experimental data collection are considered ... [Pg.109]

As eqns 3.3 and 3.4 show, the rate is obtained directly from the effluent concentration at given reactor volume, feed concentration, and flow rate, without a finite-difference approximation as for a batch reactor in eqn 3.1 or 3.2. This has important implications for the choice of the evaluation method (see Section 3.3). [Pg.38]

What are the necessary feed solution concentration and flow rate From Equation 2.10 ... [Pg.28]

How many values of the concentrations and flow rates variables in the process shown in the figure are unknown List them. The streams contain two components, 1 and 2. [Pg.133]


See other pages where Flow rate and concentration is mentioned: [Pg.3055]    [Pg.253]    [Pg.238]    [Pg.156]    [Pg.275]    [Pg.198]    [Pg.445]    [Pg.197]    [Pg.1598]    [Pg.403]    [Pg.278]    [Pg.292]    [Pg.4]    [Pg.108]    [Pg.197]    [Pg.334]    [Pg.42]    [Pg.287]    [Pg.67]    [Pg.487]    [Pg.540]    [Pg.299]    [Pg.548]    [Pg.128]    [Pg.999]    [Pg.594]   


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Balances Written in Terms of Concentration and Molar Flow Rate

Concentrate flow

Rate concentrations

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