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As function of temperature, Fig

We now consider the influence of the support material on the reactivity of the three atoms. The experiments show that the coinage metal atom silver remains inert when deposited on the MgO surface and exposing this model system to 1 Langmuir of acetylene at 90 K and detecting benzene as function of temperature (Fig. 1.100). Thus, the electronic structure of Ag is not substantially changed even when trapped at an F center. Calculations... [Pg.169]

A number of DMA analyses are discussed in Sect. 4.5.5. They deal with amorphous poly(methyl methacrylate) and a polycarbonate and their frequency dependencies as functions of temperature (Fig. 4.162-165 and Fig. 4.16 169, respectively) and poly(vinyl chloride) with a glass uransition (T = 370 K) and some local motion at about 200 K (see Fig. 4.170). [Pg.584]

By varying the heating rates, the effective activation energies of segmental motion, Q, in both POM [21,210] and HDPE [15,209] were determined as functions of temperature (Fig. 47). One can see that these dependencies are different and are characterized by broad dispersions of Q values varying from 50-60 to 280-330 kJ mol Three distinct relaxation regions can be seen. These results allowed us to make the undisputable assignments to relaxations I, II, and III. [Pg.151]

Fig. 40. Indentation hardness, at A, 19 )J.ni B, 47 jJm and C, 108 ]lni thickness, and Young s modulus, E, of a free film (as functions of temperature) of an acryhc coating (249). These results show the dependence of thickness that occurs with thin films. To convert MPa to psi, multiply by 145. Fig. 40. Indentation hardness, at A, 19 )J.ni B, 47 jJm and C, 108 ]lni thickness, and Young s modulus, E, of a free film (as functions of temperature) of an acryhc coating (249). These results show the dependence of thickness that occurs with thin films. To convert MPa to psi, multiply by 145.
Example. — Ice and water-vapour are in equilibrium at + 0 0077° C., under a pressure of 4 57 mm., and liquid water is in equilibrium with water-vapour at the same temperature and pressure ice, liquid water, and water-vapour are therefore in equilibrium under these conditions, and the equilibrium curves representing pressures as functions of temperature meet at a triple point (0 0077° C., 4 57 mm.). These curves are (Fig. 47) ... [Pg.214]

Electrical conductivity measurements revealed that ionic conductivity of Ag-starch nanocomposites increased as a function of temperature (Fig.l7) which is an indication of a thermally activated conduction mechanism [40]. This behavior is attributed to increase of charge carrier (Ag+ ions) energy with rise in temperature. It is also foimd to increase with increasing concentration of Ag ion precursor (inset of Fig.l7). This potentiality can lead to development of novel biosensors for biotechnological applications such as DNA detection. [Pg.138]

The role of the substrate temperature can be inferred from a plot of /J2 ev and R versus max at the three temperatures mentioned 200, 250, and 300°C (see Figure 49). At a substrate temperature of 200°C the refractive index is lower at every max than at a substrate temperature of 250°C. Further, the threshold at which dense material is obtained is observed to be a few electron volts higher than at 250°C. The refractive index at 300°C is high and independent of max-The microstructure parameter R as a function of max behaves similarly for material deposited at 200 and at 250°C. At 300°C the value of R is less than 0.1 and independent of max- It is noteworthy to show the relation between the internal stress and max as a function of temperature (Fig. 50). The stress is linearly... [Pg.125]

Mossbauer spectroscopy is particularly suitable to study ST since (1) the spectral parameters associated with the HS and LS states of iron(II) clearly differ and (2) the time-scale of the technique ( 10 s) allows the detection of the separate spin states in the course of the transition. Typically, Mossbauer spectra of HS iron(II) show relatively high quadrupole splitting (AEq 2-3 mm s ) and isomer shift (3 1 mm s ), while for LS iron(II), these parameters are generally smaller (AEq < 1 mm s 3 < 0.5 mm s ). Among the early applications of Mossbauer spectroscopy to study ST phenomena in iron(II) complexes is the work of Dezsi et al. [7] on [Fe (phen)2(NCS)2] (phen = 1,10-phenanthroline) as a function of temperature (Fig. 8.2). The transition from the HS ( 12) state (quadrupole doublet of outer two lines with AEq 3 mm s ) to the LS CAi) state (quadrupole... [Pg.394]

Fig. 51 Phase diagram for PS-PI diblock copolymer (Mn = 33 kg/mol, 31vol% PS) as function of temperature, T, and polymer volume fraction, cp, for solutions in dioctyl ph-thalate (DOP), di-n-butyl phthalate (DBP), diethyl phthalate (DEP) and M-tetradecane (C14). ( ) ODT (o) OOT ( ) dilute solution critical micelle temperature, cmt. Subscript 1 identifies phase as normal (PS chains reside in minor domains) subscript 2 indicates inverted phases (PS chains located in major domains). Phase boundaries are drawn as guide to eye, except for DOP in which OOT and ODT phase boundaries (solid lines) show previously determined scaling of PS-PI interaction parameter (xodt

Fig. 51 Phase diagram for PS-PI diblock copolymer (Mn = 33 kg/mol, 31vol% PS) as function of temperature, T, and polymer volume fraction, cp, for solutions in dioctyl ph-thalate (DOP), di-n-butyl phthalate (DBP), diethyl phthalate (DEP) and M-tetradecane (C14). ( ) ODT (o) OOT ( ) dilute solution critical micelle temperature, cmt. Subscript 1 identifies phase as normal (PS chains reside in minor domains) subscript 2 indicates inverted phases (PS chains located in major domains). Phase boundaries are drawn as guide to eye, except for DOP in which OOT and ODT phase boundaries (solid lines) show previously determined scaling of PS-PI interaction parameter (xodt <P 1A and /OOT 0"1) dashed line dilution approximation (/odt From [162], Copyright 2000 American Chemical Society...
The thermal expansion coefficients of PVCL and a copolymer in water, tfpol> were determined by PPC as a function of temperature (Fig. 23) [180]. The plots can be divided into four temperature ranges. Below the transition temperature, 10 < T < 30 °C, g i for PVCL remains constant, while in the case of PVCL-g-34, apoi has a negative slope. In both cases, apoi undergoes a sharp... [Pg.63]

Fig. 5.20. Volumetric heat capacity of 4He and some regenerator materials as functions of temperature. [Pg.148]

Fig. 1.36.1. Electrical resistance (ER) as function of temperature during cooling and rewarming of a virus suspension. The suspension subcools from -10 °C to approx. -46 °C and freezes at -60 °C to -65 °C. During rewarming the resistance drops clearly at approx. -33 °C. This product should be freeze dried at rice = -40 °C or a little higher (Fig. 7 from [1.27]). Fig. 1.36.1. Electrical resistance (ER) as function of temperature during cooling and rewarming of a virus suspension. The suspension subcools from -10 °C to approx. -46 °C and freezes at -60 °C to -65 °C. During rewarming the resistance drops clearly at approx. -33 °C. This product should be freeze dried at rice = -40 °C or a little higher (Fig. 7 from [1.27]).
Fig. 1.53. Freezing and thawing plot of coffee extract with 25 % solids. UFW (g H20/g solids) as a function of temperature (Fig. 2 from [ 1.37])-I, Subcooling 2, collapse temperature. Fig. 1.53. Freezing and thawing plot of coffee extract with 25 % solids. UFW (g H20/g solids) as a function of temperature (Fig. 2 from [ 1.37])-I, Subcooling 2, collapse temperature.
Fig. 10. Complex dynamic viscosity as function of temperature for three different aliphatic hyperbranched polyesters based on bismethylol propionic acid and having different end-group structure - (O) propionate end-groups, ( ) benzoate end-groups, ( ) hydroxyl end-groups [118]... Fig. 10. Complex dynamic viscosity as function of temperature for three different aliphatic hyperbranched polyesters based on bismethylol propionic acid and having different end-group structure - (O) propionate end-groups, ( ) benzoate end-groups, ( ) hydroxyl end-groups [118]...
Fig. 21. Infrared vibrational spectra of a Ru(OOl) surface exposed to a CO/Hj mixture (1 3) at 50 torr as function of temperature and reaction time. The shift between 400 K and 300 K is caused by the change in the steady state CO coverage. (Reproduced by permission from Hoffmann and Robbins ".)... Fig. 21. Infrared vibrational spectra of a Ru(OOl) surface exposed to a CO/Hj mixture (1 3) at 50 torr as function of temperature and reaction time. The shift between 400 K and 300 K is caused by the change in the steady state CO coverage. (Reproduced by permission from Hoffmann and Robbins ".)...
Behm et al. have measured LEED diffraction intensities for H monolayers on Pd(100) surfaces as function of temperature at different coverages (Fig. 13b). Taking the temperature Ti,2 where the intensity has dropped to 50% of its low-temperature value as estimated for Td ), they constructed the phase diagram shown by crosses in Fig. 13a. (Alternatively using the inflection points of the I vs T curves (Fig. 13b) yields similar results.)... [Pg.119]

Binary data can be represented with a T—x diagram that shows the mutual solubility as function of temperature. Most of the binary systems belong to one of the classes in Fig. 10.1. For ternary systems, experimental data are usually obtained at constant temperature and given in ternary diagrams. There are many types of systems, but more than 95% belong to one of the two classes shown in Fig. 10.1. [Pg.427]

Fig. 10.1 Different types of liquid-liquid systems, (a), (b) Solubility as function of temperature for binary systems (c), (d) ternary systems. (Dashed lines are examples of tie lines, which connect the two phases in equilibrium located at the binodal.)... Fig. 10.1 Different types of liquid-liquid systems, (a), (b) Solubility as function of temperature for binary systems (c), (d) ternary systems. (Dashed lines are examples of tie lines, which connect the two phases in equilibrium located at the binodal.)...
Fig. 10.16 Solubility of naphthalene in supercritical ethene as function of temperature at different pressures. [Pg.449]

Fig- 4.10 Susceptibilities of LaCu03 and LaNi03 as functions of temperature. From Parent (1972) see also Goodenough et al (1973). [Pg.141]

Figure 6.11 shows the resistivities of some alloys (V - xCrJjC as functions of temperature. The addition of Cr, as already stated, increases the temperature at which the transition to the metallic state occurs. At higher temperatures a transition back to the semiconducting state is predicted by the phase diagram of Fig. 6.3. Particularly remarkable, however, are the very low conductivities... Figure 6.11 shows the resistivities of some alloys (V - xCrJjC as functions of temperature. The addition of Cr, as already stated, increases the temperature at which the transition to the metallic state occurs. At higher temperatures a transition back to the semiconducting state is predicted by the phase diagram of Fig. 6.3. Particularly remarkable, however, are the very low conductivities...
Fig. 52. Hole drift mobility in tri-phenylamine-Lexan films as function of temperature, x - mass ratio of the dopant to polymer A - activation energy of the hole mobility (290)... Fig. 52. Hole drift mobility in tri-phenylamine-Lexan films as function of temperature, x - mass ratio of the dopant to polymer A - activation energy of the hole mobility (290)...
Fig. 2.7. Calculated mass action constant K(T) serves to estimate dimer concentrations in hydrogen, methane, carbon dioxide and sulfur hexafluoride as function of temperature. Fig. 2.7. Calculated mass action constant K(T) serves to estimate dimer concentrations in hydrogen, methane, carbon dioxide and sulfur hexafluoride as function of temperature.
Fig. 3.27. Left Spectral moments 71 of the rototranslational bands of several molecular pairs, as function of temperature. Various measurements ( , o, etc.) are compared with theoretical data based either on the fundamental theory (H2-H2, H2-He) or on refined multipolar induction models after [58]. Right Same as at left, except the spectral moment 70 is shown. Fig. 3.27. Left Spectral moments 71 of the rototranslational bands of several molecular pairs, as function of temperature. Various measurements ( , o, etc.) are compared with theoretical data based either on the fundamental theory (H2-H2, H2-He) or on refined multipolar induction models after [58]. Right Same as at left, except the spectral moment 70 is shown.
Fig. 3.42. Spectral invariant 70 of H2-H2 as function of temperature after [281], Various measurements are shown ( o ). The solid line is computed from first principles. Fig. 3.42. Spectral invariant 70 of H2-H2 as function of temperature after [281], Various measurements are shown ( o ). The solid line is computed from first principles.
Fig. 3.44. Spectral moment 71 of the F -FIe fundamental band as function of temperature after [151]. Measurements (o, x) The curve is computed from first principles. Fig. 3.44. Spectral moment 71 of the F -FIe fundamental band as function of temperature after [151]. Measurements (o, x) The curve is computed from first principles.
A selection of computational results of binary, rototranslational moments as function of temperature is shown in Fig. 3.27, p. 100 (solid lines). For... [Pg.289]

Fig. 6.1. First and second moments of the main dipole components, A AL = 0001 (left) and 0223 (right) of the fundamental band of hydrogen in unmixed hydrogen, as function of temperature units are 10 50 erg cm6 s-1 and 10-37 erg cm6 s-2 for the first and second moments, respectively. The dot-dashed curves represent the moments obtained without accounting for the vibrational state dependence of the interaction potential [281]. Fig. 6.1. First and second moments of the main dipole components, A AL = 0001 (left) and 0223 (right) of the fundamental band of hydrogen in unmixed hydrogen, as function of temperature units are 10 50 erg cm6 s-1 and 10-37 erg cm6 s-2 for the first and second moments, respectively. The dot-dashed curves represent the moments obtained without accounting for the vibrational state dependence of the interaction potential [281].
Fig. 13.2 Predicted equilibrium concentrations as function of temperature of selected major and minor species in a typical flue gas from combustion. Fig. 13.2 Predicted equilibrium concentrations as function of temperature of selected major and minor species in a typical flue gas from combustion.

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As a function of temperature

Function of temperature

Temperature as a function

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