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Melting curves comparative

Figure Al(a) shows the constant value of porosity used in the analytic model (dashed curve), compared to the porosity distribution for a ID melt column in which the upward flux of melt is required to remain constant (see Spiegelman and Elliott 1993). The solid curves in Figure Al(b) show values of ct, calculated from equations (A12-A14) along the (dimensionless) length of the melting column for the decay chain with a constant porosity of 0.1% and solid upwelling velocity of 1 cm/yr. Figure Al(a) shows the constant value of porosity used in the analytic model (dashed curve), compared to the porosity distribution for a ID melt column in which the upward flux of melt is required to remain constant (see Spiegelman and Elliott 1993). The solid curves in Figure Al(b) show values of ct, calculated from equations (A12-A14) along the (dimensionless) length of the melting column for the decay chain with a constant porosity of 0.1% and solid upwelling velocity of 1 cm/yr.
Figure 9. Differential thermal analysis ofrecrystallized (1) and evaporated (2) MA P (a), and compared melting curves of AMA (1) and POM (2) (b). Figure 9. Differential thermal analysis ofrecrystallized (1) and evaporated (2) MA P (a), and compared melting curves of AMA (1) and POM (2) (b).
Figure 5,45 P-T stability curve of phlogopite compared with the incipient melting curves of granite and basalt. Reprinted from H. S. Yoder and H. R Eugster, Geochimica et Cos-mochimica Acta, 6, 157-185, copyright 1954, with kind permission from Elsevier Science Ltd., The Boulevard, Langford Lane, Kidlington 0X5 1GB, UK. Figure 5,45 P-T stability curve of phlogopite compared with the incipient melting curves of granite and basalt. Reprinted from H. S. Yoder and H. R Eugster, Geochimica et Cos-mochimica Acta, 6, 157-185, copyright 1954, with kind permission from Elsevier Science Ltd., The Boulevard, Langford Lane, Kidlington 0X5 1GB, UK.
Chatterjee and Johannes (1974), is compared in figure 5.47A with the experimental results of Ivanov et al. (1973) for = co2 Figure 5.47A also superimposes the melting curves of granite in the presence of a fluid phase of identical composition. Note that the composition of the fluid dramatically affects stability relations if the amount of H2O in the fluid is reduced by half = 0.5), the stability field of muscovite is re-... [Pg.333]

Figure 4-3 Experimental data on nucleation rate in lithium disilicate melt (points) compared to theory. The solid curve is a fit to the experimental data. The short dashed curve (middle curve) is the theoretically calculated curve multiplied by 1.7 xlO °. Parameters used in calculating the theoretical curve using Equation 4-9 Te=1306K, a O.ZOlJ/m, l c = 61.2cm /mol, AHm-c = 61.1 kj/mol, = (Neilson and Weinberg, 1979). The long... Figure 4-3 Experimental data on nucleation rate in lithium disilicate melt (points) compared to theory. The solid curve is a fit to the experimental data. The short dashed curve (middle curve) is the theoretically calculated curve multiplied by 1.7 xlO °. Parameters used in calculating the theoretical curve using Equation 4-9 Te=1306K, a O.ZOlJ/m, l c = 61.2cm /mol, AHm-c = 61.1 kj/mol, = (Neilson and Weinberg, 1979). The long...
Fig. 32 Unbound particle fraction as a function of temperature for colloids interacting through DNA sticky-end pairing. Experimental data for various sticky end fraction (symbols) are compared with the melting curve for the same sticky end sequence in solution blue line), much broader. The red line shows the hybridization free energy of DNA in solution right axis), while the dashed red line shows the effect of an entropy correction (see discussion in the text). Reproduced with permission from [136]... Fig. 32 Unbound particle fraction as a function of temperature for colloids interacting through DNA sticky-end pairing. Experimental data for various sticky end fraction (symbols) are compared with the melting curve for the same sticky end sequence in solution blue line), much broader. The red line shows the hybridization free energy of DNA in solution right axis), while the dashed red line shows the effect of an entropy correction (see discussion in the text). Reproduced with permission from [136]...
Estimate Tm of the sample by plotting the melting curve. Perform regression analysis to deduce the correlation between Tm and the base composition of DNA by comparing the following data of DNAs from other sources ... [Pg.36]

Nuclear magnetic resonance (NMR) can be used as a rapid alternative to differential scanning calorimetry in the determination of the solid fat content and studies on the melting behaviour. The determination is based on detection of the different populations of protons in solid and liquid phases, which indicates the hardness of the fat. Hernandez and Rutledge (1994b) used low resolution pulse NMR to compare melting curves of roasted and non-roasted cocoa butters from Africa, Indonesia and South America. Discriminant analysis techniques showed... [Pg.86]

The purpose of this chapter is 3-fold (1) to review basic principles of hybridization and the kinetics of reassociation, (2) to provide an overview that summarizes and compares different techniques used in single-copy hybridization, and (3) to examine different estimates of distance derived from melting curves. Most of the topics in this chapter are discussed in greater detail elsewhere, and readers are referred to Britten et al.,6 Sheldon and Bledsoe,7 and Werman et al.6 for consideration of specific topics. Also, we do not discuss the application of DNA hybridization data to problems in phylogenetic reconstruction, but rather refer readers to Springer and Krajewski9 and Werman et al.6... [Pg.233]

How would the melting curve for RNA compare with that for DNA ... [Pg.225]

Dimethyl Sulfoxide Use a pure grade of dimethyl sulfoxide (99.9%, melting point 18°) that has a clear, water-white appearance has an absorbance curve, compared with water, not exceeding 1.0 at 264 nm and shows no extraneous impurity peaks in the wavelength range up to 350 nm. Store in glass-stoppered bottles. [Pg.292]

In Figure 9 we present a calculated melt curve that compares favorably with our experimental results. This melt curve is the result of a minimized two-phase Gibbs free energy equation of state made to match accepted thermodynamic parameters and all available high-pressure experimental data including shock Hugoniot data [126], static cold compression volumes and compressibility from x-ray [128], and adiabatic ISLS sound velocity measiu-ements [127]. Comparisons of these data are provided in Figure 12a,b, and c. [Pg.423]

Therefore, the values of pEMe0 determined by averaging the titration data from the initial section of the titration curve (characterized by a sharp e.m.f. reduction at small titrant additions) are just the dissociation constant of the studied oxide, to an accuracy determined by the natural spread of the experimental data. It should be emphasized, however, that the values of the pEMeQ concentration constant calculated in such a way, contain an appreciable error, caused by the fact that the initial concentration of the titrant in the halide melt is comparable in magnitude with that of oxygen-containing admixtures in the pure melt. [Pg.243]

Compare this equation with the Clapeyron equation, Eq. 7.7-4.) Consequently, along the melting curve... [Pg.869]

Bi- and tetramolecular structures also give quite comparable enthalpies. However, the validity of the van t Hoff analysis for some of these quadruplexes is questionable, as the melting curve used to determine thermodynamic parameters rarely corresponds to a true equilibrium curve. We will address this point later in the manuscript. An enthalpy of formation of —21 to —26 kcal mol per quartet is found for the G2T2NT2G2 sequence in comparison to —22.5 kcal mol per quartet measured for the G4T4G4 sequence. Concerning parallel quadruplexes, analysis of the calorimetric or thermokinetic data gives a value of —72 kcal moD (ref. 27) and —76.5 kcal moD (ref. 28) for the TG4T sample... [Pg.32]

To the sample of pure w-pentane, 2.40 mole-% of isn-octane was added. The melting curve so obtained showed considerable curvature, while that for the pure n-pentane was a straight line. From the slope of the line, a purity of 97.58 mole-% was obtained compared to a theoretical value of 97.53 mole-%. [Pg.649]

Fig. 4.10. Thermal analysis and proton NMR second moment curves of trans-l,4-polybutadiene. The heat capacity for the solid (glass and low temperature crystal form I) have been computed by fitting at low temperature to an approximate skeletal vibration spectrum. The gradual decrease of the second moment of the proton resonance spectrum below T comes mainly from increasing mobility in the amorphous phase, Ref. The melting curve is of an approximately 90% crystalline sample. Ref.. Compare also to Fig. 1.3... Fig. 4.10. Thermal analysis and proton NMR second moment curves of trans-l,4-polybutadiene. The heat capacity for the solid (glass and low temperature crystal form I) have been computed by fitting at low temperature to an approximate skeletal vibration spectrum. The gradual decrease of the second moment of the proton resonance spectrum below T comes mainly from increasing mobility in the amorphous phase, Ref. The melting curve is of an approximately 90% crystalline sample. Ref.. Compare also to Fig. 1.3...
In hydrogen, the interaction between molecules is weak as compared to other gases, therefore the critical temperature is low (Tc = 33.0K). The melting curve, the solid-liquid boundary in a p-T diagram, has been determined by several groups... [Pg.75]

A linear approach for both the temperature and pressure dependency of the chemical potential is sufficient for calculating the melting pressure curve (compare Sect. 5.4). For the process... [Pg.309]

It is also interesting that a real heteropolymer with a non-uniform primary structme does not melt as sharply as a specially prepared homopolymer. Figure C5.13 explains why. It compares polymers with different primary structmes showing their melting curves. These are dependencies of the helical fraction (sometimes also called helicity it is the fraction of helical units in the chain) on inverse temperature Two imiform homopolymers, say A A. .. A and B B. .. B, both melt rather... [Pg.74]


See other pages where Melting curves comparative is mentioned: [Pg.395]    [Pg.228]    [Pg.444]    [Pg.252]    [Pg.163]    [Pg.160]    [Pg.246]    [Pg.129]    [Pg.29]    [Pg.262]    [Pg.240]    [Pg.770]    [Pg.1925]    [Pg.312]    [Pg.395]    [Pg.272]    [Pg.209]    [Pg.314]    [Pg.216]    [Pg.74]    [Pg.67]    [Pg.86]    [Pg.234]    [Pg.53]    [Pg.643]    [Pg.350]    [Pg.33]    [Pg.235]    [Pg.369]    [Pg.58]   
See also in sourсe #XX -- [ Pg.40 ]




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