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Eicosane temperature

FIGURE 2.1.1.1.35.1 Logarithm of vapor pressure versus reciprocal temperature for n-eicosane. [Pg.200]

Among our model compounds (Table 4.1), only a-eicosane has a Tm value that is above 25°C that is, it is the only alkane in this group that is a solid at room temperature. The three other compounds have much lower melting points, which means that, in these cases, we would have to lower the temperature at least to -29.7, -138.4, and -182.5°C in order to freeze a-decane, n-butane, and methane, respectively. [Pg.100]

Experimental values for the critical temperatures of n-alkanes are known up to eicosane (i=20) (Reid et al., 1987). For longer molecular chains the experimental determination of the critical temperature is not possible with sufficient accuracy due to the onset of thermal decomposition. [Pg.164]

The details of the EPR investigation of the graphite compound MCl6BF4M merit some discussion. Because the material is an electronic conductor, we suspended the polycrystalline sample in eicosane, melted the mixture under hot water, vibrated the sample to get random orientation, and froze the mixture under cold water. Because "CifcBF is an anisotropic conductor (it does not have metallic conductivity orthogonal to the planes), the interpretation of the EPR results requires care. Thus, in a thick plate of an isotropic metal as lithium, one observes a Dysonian asymmetry parameter A/B which is dependent on temperature, varying between... [Pg.87]

Predict the critical temperature of (a) n-eicosane, (b) 1-butene, and (c) benzene using the empirical correlation of Nokay. The Nokay relation is... [Pg.3]

Most of the fod chelates are eluted before eicosane (Figure 1). Figure 2 shows that even in the less volatile thd system, where the presence of fluorine does not complicate matters, Yb(thd)3 is eluted before tetracosane. This is shown to be the true order of volatilities of these compounds by the thermograms in Figures 3 and 4. Figure 3 shows that Eu(thd).3 vaporizes at lower temperatures than tetracosane under identical conditions, while Figure 4 indicates the volatilization at lower temperatures of Yb(thd)3 as compared with Eu(thd)3. [Pg.153]

Micelles made of soaps break up and reform within milliseconds. The individual lifetime of a charged micelle is very short. Nevertheless, eicosane sulfate micelles have been trapped by rapid cryo-fixation at liquid nitrogen temperature and freeze etching. They can then be seen under the transmission electron microscope (TEM) (Figure 2.5.3). [Pg.97]

STABILITY. The stability of the lithium in these dispersions seems high. Samples of both oil- and eicosane-dispersed products showed only surface film decomposition when stored in air at room temperature for up to 30 days. When added to water there was a steady nonviolent evolution of hydrogen. Thin films of the dispersions exposed to air at room temperature, reacted slowly over a period of days. Based on a limited observation, it seems safe to assume that lithium dispersed in the media given is no more hazardous to handle than normal solid lithium. [Pg.15]

To simulate a well-defined moleculai composite, equal weight of Cj eicosane is added into the C,2-PAM-T. Upon heating the 1 1 wt./wt. mixture, layer spacing of the polymer system is measured by WAXS. In Figure 7 is reproduced the temperature dependence of layer spacing measured by WAXS. In Figure 7 the upper curve denotes layer spacing variation of the C2o/C,2-PAM mixture and the lower one denotes that of C,2-PAM in the absence of C20 eicosane. [Pg.485]

Figure 7. Temperature dependence of layer spacing of C,-PAM, C,j-PAM+C, (Eicosane)... Figure 7. Temperature dependence of layer spacing of C,-PAM, C,j-PAM+C, (Eicosane)...
Since Cjo eicosane is very similar to the n-octoxymethyl group in chemical structure, there should be an interaction between Cjo eicosane and the C,2 side branch. This can be confirmed by the upper curve of Figure 7. This curve of Figure 7 reveals that below about 110°C, the layer spacing of the 1 1-mixture does not change practically, but at about 110°C it jumps far more than the lower cuive without C20 eicosane. This phenomenon indicates that at that temperature C20 eicosane starts to penetrate into the C,2 side chain phase and the side chains phase increase in volume and hence in the layer spacing. [Pg.490]

At higher temperatures than 110°C the rigid PAM main chain acts as a stiff fiber and the Cj2 side chain/C2o eicosane mixture can be considered as a continuous matrix phase. Both phases are dispersed molecularly to foim a molecular composite, though it is only stable at higher temperature than 110°C, because upon cooling the process returns to its original state. [Pg.490]

Chappelow and Prausnitz (15) measured the low-pressure solubilities of methane, ethane, propane, n-butane, iso-butane and hydrogen in n-hexadecane, n-eicosane, squalqne, bicyclohexyl, octamethylcyclotetraxiloxane, diphenylmethane and 1-methylnaphtha-lene over the temperature range 25 to 200 °C. They used an apparatus as that used by Cukor and Prausnitz (27). [Pg.70]

McCaim et al. recently introduced an approach that combined the process of melt co-axial electrospinning to encapsulate the phase change materials (PCMs) into polymer or composite sheath. PCM can help stabilize the temperature near its melting point as the material changes the state from a solid to liquid or vice versa and the enthalpy of fusion involved can absorb or release thermal energy. The nanofibers produced using such a material can be used in thermal insulation applications. The researchers used three PCMs, octadecane, hexadecane and eicosane, in melt forms as core solutions and demonstrated temperature stabilization at three different points, 17°C, 30°C and 37°C, respectively ... [Pg.267]

Investigations of mixtures of alkanes for C19H40-C20H42 indicate that the temperature range of the rotator phase widens due to chain mixing.Eicosane has also been studied and X-ray scattering measurements indicate the existence of a rotator phase.Studies of the ultrasonic attenuation and DSC measure-... [Pg.104]

Plot of the acoustic velocity in the chain direction (a) and the DSC trace (b) for the melting of eicosane. The dotted line in (a) indicates the linear extrapolation of the velocity from low temperature. [Pg.104]


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