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Single-parameter analysers

There are a host of commercially instruments available for the monitoring of a single parameter in both industrial and domestic water. All these instruments are very similar and only differ significantly in the sensing system used, which Is suited to the analyte (parameter) to be determined. [Pg.488]

The distillation coil has an expansion chamber partially filled with 1-mm glass beads, a bottoms draw to remove hot acid and an overhead draw to remove vapours. The cycle time includes 1 min for sampling and 3 min for washing. [Pg.491]

Turbidimetric. There are two basic types of on-line water turbidimeters surface scatter and flow-through. In turbidimeters of the former type the sample flows Into a constant-level well. The light beam is directed to the sur- [Pg.491]


A representative example of a flexible, single-parameter analyser with final transfer is the Vitatron Akes, depicted In Fig. 8.5. In the aspiration position, the sample meets the reagent or diluent stream and the reaction mixture is subsequently transferred to the measuring cuvette, from which it is flushed by the aspiration system after detection, the cuvette being suitably washed. The instrument includes a linear sample train, sample turntable, sampling head, dilutor, reagent dispenser, data-input keyboard, photometric detection system, computer, printer, evacuation pump and wash solution doser. It is prepared for kinetic measurements. [Pg.446]

We ve looked at many other analyses of "simple" processes, but my favorite is a correlation for the absorption of an acid and a base in the same equation, — not only that, but with each one at six different pH s, (Figure 2). The data are from Schurmann Turner ( ) the base is propranolol and the acid, 4-n-hexylphenylacetic. Only a single parameter is required, log D, Equation 6. Kubinyi s bilinear equation gives an even better correlation ( ), Equation 7. (This is a special version of the bilinear model which sets the coefficients of each term equal.)... [Pg.228]

Inspection of Fig. 8 shows that there is considerable scatter in the data. Part of this may be due to the fact that we are attempting to represent a complex phenomenon with a single parameter, the dispersion coefficient. Errors would also be caused by the common practice of taking measurements at or beyond the exit of the packed section. This neglect of end conditions could lead to large errors in the calculated dispersion coefficients, as pointed out by Bischoff and Levenspiel (B14). Also, all the analyses were based on the assumption of having a perfect pulse, step. [Pg.123]

In a second step, to further increase acceptance of the model, "what if..." analyses, often based on extreme scenarios or significant modifications of a single parameter, were used to generate a joint understanding of how the model reacts to parameter changes. [Pg.176]

As a general rule many of the complexities of analysing transient kinetic measurements may be circumvented by careful choice of experimental design. The objective is to employ conditions, where possible, under which the transient follows an exponential time course (or the sum of a small number of exponentials). In this circumstance the kinetic process can be described by a single parameter, a rate coefficient, which is independent of the amplitude of the transient. [Pg.115]

To follow the trend of the automation of the potentlometrlc technique, various manufacturers have launched a series of single- and multi-parameter analysers for the determination of gases and liquids, which are discussed below. [Pg.315]

Fig. 15.9 Sample and reagent flow diagrams (a) and flush (b) of a single-parameter water analyser with colorimetric detection. (Courtesy of Hach Co.). Fig. 15.9 Sample and reagent flow diagrams (a) and flush (b) of a single-parameter water analyser with colorimetric detection. (Courtesy of Hach Co.).
The problems associated with the sampling and automation of this stage were dealt with in their corresponding sections, so this section Is exclusively devoted to the automated instrumentation available for this type of sensor. As with water analysers, air analysers are classified into off- and on-line analysers, and the latter in turn Into single-parameter and multiparameter. [Pg.502]

The joint use of single- and multi-parameter analysers permits the monitoring of a variety of analytes. The instrument depicted in Fig. 15.24b is... [Pg.513]

Industrial analysers can control physical or chemical parameters. Physical parameter analysers (conductimeters, viscometers, refractometers, pressure and temperature meters) frequently measure and control only one property of the fluid, the variation of which generally depends on a single component that is controlled In an indirect fashion. Chemical parameter analysers directly measure the concentration of one or more species In a fluid. They can be specific for a given species (e.g. pH-meters, potentiometers with Ion-selective electrodes, oxygen meters) or control several species simultaneously (e.g. gas or liquid chromatographs) or successively (photometers) with minimum alterations. [Pg.531]

Single parameters incorporating connectivity are used principally in two different areas the analysis of structural and dynamic properties of molecules in conformations with conserved architecture, and molecular similarity analyses based on chemical graph theory. The descriptors used in these two areas differ conceptually, and their natures must be clarified from the start. [Pg.205]

To determine whether path (a) or path (b) correctly describes the oxidations, we carried out Hammett and modified Hammett analyses of the rate data (Table 3, Figures 9 and 10). Correlation of the second-order rate constants using a single parameter Hammett equation gives the best linear fit to The correlation, however, is markedly improved by the use of the modified dual parameter Hammett equation proposed by Dust and Amold. ... [Pg.177]

Rather, this section analyses the behavior of reported single-parameter scales developed to describe the global behavior of solvents [viz. the Z, Py, <1>, G and Er(30) scales] against the SPP, SB and SA scales on the basis of the 200 solvents listed in Table 10.3.1. The Y scale, established to describe the behavior of solvolysis-like kinetics, is dealt with in the section devoted to the description of kinetic data. The data used in this analysis were taken from the following sources those for the Z scale from the recent review paper by Marcus those for the O and G scales from the compilation in Table 7.2 of Reichardt s book those for parameter Py from flic paper by Dong and Winnik and those for Er(30) from the recent review by Reichardt or Table 7.3 in his book. ... [Pg.605]

For the purpose of this paper we only look into single parameter sensitivity analyses, i.e. the effects of changing one parameter at the time. [Pg.1661]

Attenq>ts have also been made to use relatively complex simulation approaches superpositioning the effects of various processes and events. However, the more mpirical approach, based on selected combinations of events and processes, has to date been directly applied in more numerous and more specific analyses. Both approaches have run into similar problems when trying to tackle the important issue of assignment of probabilities to single parameters, to overall scenarios, or to calculated risks. [Pg.244]


See other pages where Single-parameter analysers is mentioned: [Pg.488]    [Pg.489]    [Pg.510]    [Pg.515]    [Pg.157]    [Pg.783]    [Pg.488]    [Pg.489]    [Pg.510]    [Pg.515]    [Pg.157]    [Pg.783]    [Pg.159]    [Pg.230]    [Pg.75]    [Pg.1220]    [Pg.110]    [Pg.163]    [Pg.259]    [Pg.321]    [Pg.550]    [Pg.33]    [Pg.137]    [Pg.741]    [Pg.33]    [Pg.230]    [Pg.240]    [Pg.445]    [Pg.445]    [Pg.450]    [Pg.504]    [Pg.297]    [Pg.99]    [Pg.244]    [Pg.365]    [Pg.171]    [Pg.397]    [Pg.115]   


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