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Isothermal analysis

A. C. Fewis, K. D. Bartle and F. Rattner, High-speed isothermal analysis of atmospheric isoprene and DMS using online two-dimensional gas cliromatogr aphy . Environ. Sci. Technol. 31 3209-3217 (1997). [Pg.73]

In Proceedings of 21st SemiTherm Symposium, San Jose, 15-17 March 2005, pp 1-7 Copeland D, Behnia M, Nakayama W (1997) Manifold micro-channel heat sinks isothermal analysis. IEEE Trans Comp Packag Manuf Technol A 20 96-102 Dupont V, Thome JR, Jacobi AM (2004) Heat transfer model for evaporation in microchannels. [Pg.93]

FIGURE 2.8. Typical Results of Autocatalytic Thermokinetics as Obtained by Isothermal Analysis. [Pg.25]

To what extent are assumptions of a constant x valid Table II shows the observed macroscopic proton coefficients for cation and anion adsorption in a variety of heterogeneous systems. The coefficients were determined by Kurbatov plots ( 6) or by isotherm analysis ( 7), unless otherwise indicated. In all cases, x is not an integer. [Pg.167]

The macroscopic proton coefficient may be determined by graphical analysis of observed system variables according to two different procedures fractional adsorption edge linearization (6) and isotherm analysis (7 ). The procedures for calculating the macroscopic proton coefficients according to these two methods are discussed in detail below, as are their relative advantages and disadvantages for use in semi-empirical descriptions of adsorption. [Pg.169]

THE MATHEMATICAL DEVELOPMENT OF ISOTHERM ANALYSIS FOR THE MACROSCOPIC PROTON COEFFICIENT, Xp... [Pg.187]

Table II presents our final results. We only report the four isotherms which were definitely vapor-liquid and we present both isothermal analysis and surface analysis values. Table II presents our final results. We only report the four isotherms which were definitely vapor-liquid and we present both isothermal analysis and surface analysis values.
Setting y =0.002 m, which is located in the middle of the channel and using the above data, we get a temperature of 306.6°C, a 6.6 K temperature rise. Although there is a measurable temperature rise in this system, it is not significant enough to warrant a non-isothermal analysis. [Pg.249]

The behaviour of landfill liners with respect to metal sorption has also been investigated by the novel technique of combined sequential extraction-sorption isotherm analysis (CSSA) (Salim et al, 1996). The study demonstrated that Pb and Ni would be effectively immobilised by the clayey calcareous sediment studied, but Cr would not. Roehl and Czurda (1998) applied a similar approach in their investigation of clay landfill liners and showed that speciation was dependent on heavy metal load, with weaker binding at higher concentrations of Cd and Pb. [Pg.284]

K. Grob and K. Grob, Jr., Isothermal analysis on capillary columns without stream splitting, J. Chromatogr., 94 53-64 (1974). [Pg.66]

Figure 4.6b), and NLDFT method (Figure 4.6c). All these PSDs were obtained using the software provided by the manufacturer of the commercial volumetric analyzer, where the N2 adsorption isotherms were measured. Note that CMS1, for the reason commented before (lack of N2 adsorption at 77 K due to diffusional problems), cannot be analyzed. The three methods qualitatively show the same evolution of the PSD, that is, the expected one deduced from the N2 adsorption isotherm analysis. The micropore size and the width of the distribution increase in the order ACF1 < AC2 < AC1. [Pg.136]

In order to achieve the same degree of separation in an isothermal analysis as in a programmed temperature run, a temperature 45 °C below the retention temperature of a pair of peaks should be selected. [Pg.193]

If the standard BET procedure is to be used, it should be established that monolayer-multilayer formation is operative and is not accompanied by micropore filling (Section 11.2.1.8.C), which is usually associated with an increase in the value of C (>200, say). It should be appreciated that the BET analysis does not take into account the possibility of micropore filling or penetration into cavities of molecular size. These effects can thus falsify the BET surface areas and in case of doubt their absence should be checked by means of an empirical method of isotherm analysis or by using surface area reference samples (see Section 11.2.1.6.B). [Pg.527]

The effects of antioxidants on OT of SME by non-isothermal (conventional) DSC, static mode P-DSC, and dynamic mode P-DSC were investigated by Dunn (2006a), which is summarized in Table 1.15. Results from all three methods consistently showed that treating SME with antioxidants TBHQ and a-tocopherol increased OT with respect to untreated SME. Statistical comparison of P-DSC results with those from isothermal analysis of OSI at 60°C was facilitated by calculation of the corresponding response factors (defined ratios of OT of the sample to that of methyl oleate, and of OSI of the sample to that of methyl oleate). Data for the sample and reference material (methyl oleate) were measured under the same experimental conditions. Results showed the highest degree of correlation (P = 0.79) between dynamic-mode P-DSC and isothermal OSI analyses. [Pg.39]

In principle, the as-method is not restricted to nitrogen adsorption and can be applied to any gas-solid physisorption system irrespective of the shape of its isotherm it can be used to check the validity of the BET area and also to identify the individual mechanisms (monolayer-multilayer adsorption, micropore filling or capillary condensation). Numerous examples of different as-plots are to be found in subsequent chapters. Here, we are concerned with the general principles of the as-method of isotherm analysis with particular reference to the evaluation of surface area. The distinctive features of various hypothetical as-plots are revealed in Figure... [Pg.177]


See other pages where Isothermal analysis is mentioned: [Pg.225]    [Pg.283]    [Pg.168]    [Pg.131]    [Pg.566]    [Pg.253]    [Pg.155]    [Pg.304]    [Pg.238]    [Pg.162]    [Pg.164]    [Pg.172]    [Pg.186]    [Pg.440]    [Pg.138]    [Pg.329]    [Pg.99]    [Pg.49]    [Pg.283]    [Pg.641]    [Pg.179]    [Pg.110]    [Pg.528]    [Pg.375]    [Pg.114]    [Pg.165]    [Pg.174]   
See also in sourсe #XX -- [ Pg.487 ]




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Adsorption isotherms frontal analysis

Adsorption isotherms linear least squares analysis

Amorphous solids isotherm analysis

Analysis Using Standard Isotherms

Analysis of adsorption isotherms on hypercrosslinked polystyrenes

Brunauer-Emmett-Teller method, isotherm analyses

Celluloses isotherm analyses

Excipient compatibility analysis using isothermal calorimetry

Frontal Analysis isotherm measurements

Isotherm analysis

Isotherm analysis

Isotherm frontal analysis

Isothermal Analysis of Experimental Rate Data

Isothermal gravimetric analysis

Isothermal kinetic analysis

Isothermal ligand binding analysis

Isothermal thermogravimetric analysis

Isothermal titration calorimetry interaction analysis methods

Isotherms sorption analysis

Kinetic Analysis of Isothermal Data

Kinetic analysis of non-isothermal rate measurements

Ligand binding analysis, isothermal titration

Ligand binding analysis, isothermal titration calorimetry

Non-Isothermal Analysis

Non-isothermal Kinetic Analysis Method

Plug flow reactors isothermal data, analysis

Quasi-isothermal analysis

Stepwise isothermal analysis

Thermal stability Isothermal gravimetric analysis

Thermogravimetric analysis isotherms

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