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Indicator concentration, effect

In this experiment the concentrations of Ga + and Mg + in aqueous solutions are determined by titrating with EDTA. The titration is followed spectrophotometrically by measuring the absorbance of a visual indicator. The effect of changing the indicator, the pH at which the titration is carried out, and the relative concentrations of Ga + and Mg + are also investigated. [Pg.359]

Figure 4 indicates the effect of the CTAB concentration on the rate constant of the complexes of 29 and 32. The CMC of CTAB is near 1 x 10 3 M. Below CMC, the rates cannot be measured because of insolubility of the ligands. Although unmeasured, the rates of the 29 and 32 complexes must be greatly enhanced in the presence of CTAB micelles up to CMC, but further increase of the micelle concentration above CMC cause a rate decrease. This type of micellar effect can be seen in many micellar reactions 27). Hence, it should be noted that the rate constants in Table 3 would be several times larger if they are measured by using a lower concentration of CTAB than 5 x 10-3 M. [Pg.157]

Figure 5a indicates the effect of the CTAB concentration on the rate constants of the complexes of 38b and 38c. In the case of the water soluble 38b ligand, the rate increases with increasing CTAB concentration up to a saturation level. This type of saturation kinetics is usually interpreted to show the incorporation of a ligand-metal ion complex into a micellar phase from a bulk aqueous phase, and the catalytic activity of the complex is higher in the micellar phase than in the aqueous phase. In the case of lipophilic 38c, a very similar curve as in Fig. 4 is obtained. At a first glance, there appears to be a big difference between these two curves. However, they are rather common in micellar reactions and obey the same reaction mechanism 27). [Pg.158]

The pH will depend upon the ionic strength of the solution (which is, of course, related to the activity coefficient — see Section 2.5). Hence, when making a colour comparison for the determination of the pH of a solution, not only must the indicator concentration be the same in the two solutions but the ionic strength must also be equal or approximately equal. The equation incidentally provides an explanation of the so-called salt and solvent effects which are observed with indicators. The colour-change equilibrium at any particular ionic strength (constant activity-coefficient term) can be expressed by a condensed form of equation (4) ... [Pg.264]

Glaser and Lichtenstein (G3) measured the liquid residence-time distribution for cocurrent downward flow of gas and liquid in columns of -in., 2-in., and 1-ft diameter packed with porous or nonporous -pg-in. or -in. cylindrical packings. The fluid media were an aqueous calcium chloride solution and air in one series of experiments and kerosene and hydrogen in another. Pulses of radioactive tracer (carbon-12, phosphorous-32, or rubi-dium-86) were injected outside the column, and the effluent concentration measured by Geiger counter. Axial dispersion was characterized by variability (defined as the standard deviation of residence time divided by the average residence time), and corrections for end effects were included in the analysis. The experiments indicate no effect of bed diameter upon variability. For a packed bed of porous particles, variability was found to consist of three components (1) Variability due to bulk flow through the bed... [Pg.98]

Mathew and Pillai observed a threefold increase in plutonium concentration at low, normal, and high carbonate concentrations when 20mg/liter of organic matter were added to sea water samples (29). Again this indicates the effect of organic complexation upon plutonium solubility in natural waters. [Pg.311]

The effect of temperature on adsorption was also stndied. At low temperatnre (i.e., near 0°C) adsorption proceeds very slowly, while at high temperatnre (40°C) the snrface coverage varies strongly from sample to sample, indicating side effects snch as partial desorption. Final valnes of always approached 30%, independent of the temperatnre. The effects of concentration and temperature on the surface coverage are clearly not compatible with a description of the adsorption behavior by Fangmnir s eqnation. [Pg.231]

Figure 4, Effect of sample concentration on the distribution of milk proteins on Spherogel TSKSW 2000 column. Instant, nonfat, dry milk was dissolved in mobile phase at the indicated concentrations and 10-fjJL aliquots injected under the conditions outlined in Figure 1. Figure 4, Effect of sample concentration on the distribution of milk proteins on Spherogel TSKSW 2000 column. Instant, nonfat, dry milk was dissolved in mobile phase at the indicated concentrations and 10-fjJL aliquots injected under the conditions outlined in Figure 1.
It best indicates the effectiveness of different strategies to reduce the concentration of indoor radon. The radon production rate for the whole dwelling was measured as 280 Bq m 3 h"1, with all internal doors open. [Pg.539]

As these examples indicate, the characteristic flavor of a food, fruit, etc., usually derives from a complex mixture of components. In a few cases, one unique sulfur compound is a character-impact compound, a material recognized as having the same organoleptic character as the material itself. Although some 670 compounds, of which more than 100 are sulfur-containing, have been identified in roast coffee, one material, furfurylmercaptan (2-furylmethanethiol) is considered to be a character-impact compound.43,44 The threshold level for detection of 2-furylmethanethiol in water is 0.005 ppb, and at levels of 0.01-0.5 ppb, it has the very characteristic aroma of freshly roasted coffee. However, as in many other cases, there is a concentration effect. At levels from 1-10 ppb the aroma is that of staled coffee with a sulfury note .43 Hence, 2-furylmethanethiol has a two headed property - at low concentrations it is a character impact compound and at higher levels it is an off-flavor component. [Pg.683]

It has been shown that carbon dioxide also increases the toxicity of the other gases currently included in the model. For example, the 30 minute plus 24 hour LC50 value of HCN decreases to 75 ppm and that of 02 increases to 6.6% in the presence of 5% C02. However, we empirically found that the effect of the C02 can only be added into this equation once. At this time, we have data on the effect of various concentrations of C02 on CO and only have information on the effect of 5% C02 on the other gases. Since CO is the toxicant most likely to be present in all real fires, we have included the C02 effect into the CO factor. As more information becomes available, the N-Gas equation will be changed to indicate the effect of C02 on the other gases as well. [Pg.5]

In this expression, k is the rate constant (for the chemical reaction at a given temperature). The exponents, m and n, are the orders of reaction. The orders indicate what effect a change in concentration of that particular reactant species will have on the reaction rate. If, for example, m = 1 and n = 2, then if the... [Pg.189]

In this expression, k is the rate constant—a constant for each chemical reaction at a given temperature. The exponents m and n, called the orders of reaction, indicate what effect a change in concentration of that reactant species will have on the reaction rate. Say, for example, m = 1 and n = 2. That means that if the concentration of reactant A is doubled, then the rate will also double ([2]1 = 2), and if the concentration of reactant B is doubled, then the rate will increase fourfold ([2]2 = 4). We say that it is first order with respect to A and second order with respect to B. If the concentration of a reactant is doubled and that has no effect on the rate of reaction, then the reaction is zero order with respect to that reactant ([2]° = 1). Many times the overall order of reaction is calculated it is simply the sum of the individual coefficients, third order in this example. The rate equation would then be shown as ... [Pg.199]

Figure 3. PI staining A) Cell-cycle profiles after 24 hours treatment with indicated concentrations of SN-38 or edotecarin B) Cell cycle effects on HCT-116 with time course to 24 hours. Arrows indicated position. Figure 3. PI staining A) Cell-cycle profiles after 24 hours treatment with indicated concentrations of SN-38 or edotecarin B) Cell cycle effects on HCT-116 with time course to 24 hours. Arrows indicated position.
Figure 4.4 Effect of TFA concentration on peptide retention. A series of five synthetic peptides containing 0, 1,2, 4, or 6 basic residues were separated on an octadecyl reversed-phase column using a 1%/min linear gradient from water to acetonitrile. Both solvents contained TFA at the indicated concentrations. (Reproduced from D. Guo, C.T. Mant, and R.S. Hodges, J. Chromatogr., 386 205 [1987]. With permission from Elsevier Science.)... Figure 4.4 Effect of TFA concentration on peptide retention. A series of five synthetic peptides containing 0, 1,2, 4, or 6 basic residues were separated on an octadecyl reversed-phase column using a 1%/min linear gradient from water to acetonitrile. Both solvents contained TFA at the indicated concentrations. (Reproduced from D. Guo, C.T. Mant, and R.S. Hodges, J. Chromatogr., 386 205 [1987]. With permission from Elsevier Science.)...
There are four widely accepted theories of shape selectivity reactant shape selectivity (RSS), product shape selectivity (PSS), transition state selectivity (TSS) (Figure 12.2), and concentration effect all of them are based on the hypothesis that the reactions occur within the zeolite micropores only. As indicated earlier, this hypothesis is often verified, the external surface area of the commonly used zeolites being much lower (one to two orders of magnitude) than their internal surface area. ... [Pg.236]

EIG. 10. Cyclic voltammograms illustrating the effect of supporting electrolyte concentration at a lONEE. 5 pM TMAFc in aqueous NaNOs at the indicated concentrations of NaNOs. Scan rate = 100 mV s h... [Pg.23]

In a final RTD experiment, a sheet of dye was frozen as before and positioned in the feed channel perpendicular to the flight tip. The sheet positioned the dye evenly across the entire cross section. After the dye thawed, the extruder was operated at five rpm in extrusion mode. The experimental and numerical RTDs for this experiment are shown in Fig. 8.12, and they show the characteristic residence-time distribution for a single-screw extruder. The long peak indicates that most of the dye exits at one time. The shallow decay function indicates wall effects pulling the fluid back up the channel of the extruder, while the extended tail describes dye trapped in the Moffat eddies that greatly impede the down-channel movement of the dye at the flight corners. Moffat eddies will be discussed more next. Due to the physical limitations of the process, sampling was stopped before the tail had completely decreased to zero concentration. [Pg.345]

Available information on DEHPA indicates an effect of salt concentration similar to that shown for the carboxylic acids [17]. Figure 7.11 indicates a significant difference between sodium and ammonium salts and solutions containing sodium and ammonium hydroxides. Moreover, below about 5 wt% salt concentration, the solubility becomes uneconomic. However, all the data given in Fig. 7.11 are for alkaline systems. For acid systems... [Pg.308]

A Yes count of 16 would indicate complete degradability of all components at listed conditions - concentration effect shown in row pairs. [Pg.59]


See other pages where Indicator concentration, effect is mentioned: [Pg.562]    [Pg.409]    [Pg.383]    [Pg.365]    [Pg.210]    [Pg.71]    [Pg.145]    [Pg.663]    [Pg.381]    [Pg.688]    [Pg.81]    [Pg.54]    [Pg.1658]    [Pg.119]    [Pg.328]    [Pg.55]    [Pg.576]    [Pg.363]    [Pg.277]    [Pg.223]    [Pg.27]    [Pg.471]    [Pg.64]    [Pg.160]    [Pg.141]    [Pg.142]    [Pg.211]    [Pg.361]    [Pg.535]    [Pg.342]   


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