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Concentration indicators

Freshly opened bottles of these reagents are generally of the concentrations indicated in the table. This may not be true of bottles long opened and this is especially true of ammonium hydroxide, which rapidly loses its strength. In preparing volumetric solutions, it is well to be on the safe side and take a little more than the calculated volume of the concentrated reagent, since it is much easier to dilute a concentrated solution than to strengthen one that is too weak. [Pg.1183]

Activators enhance the adsorption of collectors, eg, Ca " in the fatty acid flotation of siUcates at high pH or Cu " in the flotation of sphalerite, ZnS, by sulfohydryl collectors. Depressants, on the other hand, have the opposite effect they hinder the flotation of certain minerals, thus improving selectivity. For example, high pH as well as high sulfide ion concentrations can hinder the flotation of sulfide minerals such as galena (PbS) in the presence of xanthates (ROCSS ). Hence, for a given fixed collector concentration there is a fixed critical pH that defines the transition between flotation and no flotation. This is the basis of the Barsky relationship which can be expressed as [X ]j[OH ] = constant, where [A ] is the xanthate ion concentration in the pulp and [Oi/ ] is the hydroxyl ion concentration indicated by the pH. Similar relationships can be written for sulfide ion, cyanide, or thiocyanate, which act as typical depressants in sulfide flotation systems. [Pg.49]

Florfenicol concentrations in tissues and body fluids of male veal calves were studied after 11 mg/kg intramuscular doses adininistered at 12-h intervals (42). Concentrations of florfenicol in the lungs, heart, skeletal muscle, synovia, spleen, pancreas, large intestine, and small intestine were similar to the corresponding semm concentrations indicating excellent penetration of florfenicol into these tissues. Because the florfenicol concentration in these tissues decreased over time as did the corresponding semm concentrations, it was deemed that florfenicol equiUbrated rapidly between these tissues and the blood. Thus semm concentrations of florfenicol can be used as an indicator of dmg concentrations in these tissues. [Pg.517]

An investigation of the physical-chemical properties and IR spectra of melts with relatively low metal concentrations indicated that heptafluorometalate ions, TaF72, are also present in the melt. These measurements initiated the second conceptual step and it was assumed that there are two types of complex ions, namely octafluorometalate, MeF83 , and heptafluorometalate, MeF72, that determine the melt s various properties. [Pg.136]

Figure 2. Determination of reaction order for Pu(IV) polymer growth stage at 50° C. Sloped 3 for all HNO, concentrations indicated. (Reprinted with permission from Ref. 2.)... Figure 2. Determination of reaction order for Pu(IV) polymer growth stage at 50° C. Sloped 3 for all HNO, concentrations indicated. (Reprinted with permission from Ref. 2.)...
FIGURE 13.8 (a) When the rates of disappearance of NO, are plotted against its concentration, a straight line is not obtained, (hi However, a straight line is obtained when the rates are plotted against the square of the concentration, indicating that the rate is directly proportional to the square of the concentration. [Pg.656]

O2, Mn, pH, and solid concentrations indicates that the character of the solid is important partly because some surfaces bind Mn " more strongly and partly because they facilitate the electron transfer differently. Catalysis by enzymes is clearly the most effective oxidation enhancing process as indicated by the laboratory studies with spores and material from the O2/H2S interface of Saanich Inlet. Microbial catalysis in this environment reduces the oxidation lifetime of Mn to about one day. This example illustrates... [Pg.433]

This is consistent with the observed products of oxidation, i.e. benzyl alcohol, benzaldehyde and benzoic acid and with the observed oxidation of cyclohexane. Radical-cations are, however, probably formed in oxidation of napthalene and anthracene. The increase of oxidation rate with acetonitrile concentration was intepreted in terms of a more reactive complex between Co(III) and CH3CN. The production of substituted benzophenones at high CH3CN concentration indicates the participation of a second route of oxidation. [Pg.373]

A complex was detected in these solutions with the composition CuCN but this was not formed in significant quantities under the conditions employed. The role of ammonia molecules could not be assessed, although it was found that the rate showed a strong inverse dependence in ammonia concentration, indicating competition between NHj and CN for coordination sites. [Pg.411]

Fig. 2.33. H2Saq concentration.s as a function of temperature for hot spring fluids at midocean ridges as a function of redox. Assuming AMPC (anhydrite-magnetite-pyrite-calcite) and PPM (pyrite-pyrrhotite) buffers redox in sub-seafloor reaction zones and a pressure of 500 bars, dissolved H2Saq concentrations indicate temperatures of approximately 370-385°C. Solid star Okinawa. (Modified after Seyfried and Ding, 1995.)... Fig. 2.33. H2Saq concentration.s as a function of temperature for hot spring fluids at midocean ridges as a function of redox. Assuming AMPC (anhydrite-magnetite-pyrite-calcite) and PPM (pyrite-pyrrhotite) buffers redox in sub-seafloor reaction zones and a pressure of 500 bars, dissolved H2Saq concentrations indicate temperatures of approximately 370-385°C. Solid star Okinawa. (Modified after Seyfried and Ding, 1995.)...
Increased total, direct, and indirect bilirubin concentrations indicate defects in transport, conjugation, or excretion of bilirubin. [Pg.328]

Figures 8 and 9 show the first order kinetic plots for the isomerization and crosslinking reactions, respectively. In the data analysis the area of the isoimide peak was measured between consistent limits chosen to exclude any contribution from the 1775 cm imide band. These data were generated by measuring the area of the appropriate peak in a baseline corrected spectrum and ratioing this area to that of a reference peak (which was invarient during the experiment) in the same spectrum. This concentration indicative number was then ratioed to the concentration ratio observed on the initial scan. Plots of the log of the ratio of the concentration of the functionality at time "t" to the concentration of the functionality at t = 0 were then constructed. In order to insure that the trends in the data were not artifacts of this procedure or of the baseline correction routine, we also plotted the data in terms of peak intensity in absorbance units and observed the same trends but with more scatter in the data. Figures 8 and 9 show the first order kinetic plots for the isomerization and crosslinking reactions, respectively. In the data analysis the area of the isoimide peak was measured between consistent limits chosen to exclude any contribution from the 1775 cm imide band. These data were generated by measuring the area of the appropriate peak in a baseline corrected spectrum and ratioing this area to that of a reference peak (which was invarient during the experiment) in the same spectrum. This concentration indicative number was then ratioed to the concentration ratio observed on the initial scan. Plots of the log of the ratio of the concentration of the functionality at time "t" to the concentration of the functionality at t = 0 were then constructed. In order to insure that the trends in the data were not artifacts of this procedure or of the baseline correction routine, we also plotted the data in terms of peak intensity in absorbance units and observed the same trends but with more scatter in the data.
Figures 7.57a-c show the acceptor, donor, and reference spectra of 48 pM propranolol at the end of 15 h PAMPA assay using 20% wt/vol soy lecithin in dode-cane. The sum of the donor (3 pM) and the acceptor (<1 pM) well concentrations indicates that 45 pM is lost to the membrane. In the absence of sink-creating surfactant, only a trace of propranolol reached the acceptor wells at the end of 15 h, with 94% of the compound trapped in the membrane, compared to 19% in the 2% wt/vol DOPC case (Table 7.5). The effective permeability in 20% soy dropped to 1.8 x 10 6cm/s, compared to the DOPC value of 10.2 x 10 6cm/s. Figures 7.57a-c show the acceptor, donor, and reference spectra of 48 pM propranolol at the end of 15 h PAMPA assay using 20% wt/vol soy lecithin in dode-cane. The sum of the donor (3 pM) and the acceptor (<1 pM) well concentrations indicates that 45 pM is lost to the membrane. In the absence of sink-creating surfactant, only a trace of propranolol reached the acceptor wells at the end of 15 h, with 94% of the compound trapped in the membrane, compared to 19% in the 2% wt/vol DOPC case (Table 7.5). The effective permeability in 20% soy dropped to 1.8 x 10 6cm/s, compared to the DOPC value of 10.2 x 10 6cm/s.
The breakthrough time observed in the NOx concentration profile (obtained by addition of the NO and N02 concentrations) indicates that during the initial part of the pulse, the NO fed to the reactor is completely stored on the catalyst surface. [Pg.183]


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See also in sourсe #XX -- [ Pg.224 ]




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