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Glass binary mixture

Adsorption phenomena from solutions onto sohd surfaces have been one of the important subjects in colloid and surface chemistry. Sophisticated application of adsorption has been demonstrated recently in the formation of self-assembhng monolayers and multilayers on various substrates [4,7], However, only a limited number of researchers have been devoted to the study of adsorption in binary hquid systems. The adsorption isotherm and colloidal stabihty measmement have been the main tools for these studies. The molecular level of characterization is needed to elucidate the phenomenon. We have employed the combination of smface forces measmement and Fomier transform infrared spectroscopy in attenuated total reflection (FTIR-ATR) to study the preferential (selective) adsorption of alcohol (methanol, ethanol, and propanol) onto glass surfaces from their binary mixtures with cyclohexane. Om studies have demonstrated the cluster formation of alcohol adsorbed on the surfaces and the long-range attraction associated with such adsorption. We may call these clusters macroclusters, because the thickness of the adsorbed alcohol layer is about 15 mn, which is quite large compared to the size of the alcohol. The following describes the results for the ethanol-cycohexane mixtures [10],... [Pg.3]

Binary mixtures of glass ballotini and steel beads of nearly equal size (-500 pm and -275 pm, respectively) also exhibit reduced electrostatic activity, as measured by suspended electrodes (Guardiolaet al., 1992). The highly conducting steel beads were added to the glass particles in amounts up to approximately 10% by volume. [Pg.836]

Liquid-Glass Transition in a Lennard-Jones Binary Mixture. [Pg.157]

Equilibrium Phase Behaviour. Phase studies were performed using approximately 10 g samples of oil-surfactant mixture diluted sequentially by the weighed addition of water. The initial binary mixture contained 5-70 w/w surfactant at 5 intervals. Phase boundaries were determined to + 0.5 water. The ternary mixtures in Pyrex glass tubes fitted with PTFE lined caps were equilibrated to the required temperature (20-65 0.1°C) for 2 hours and then thoroughly mixed for 5 minutes using a Fisons orbitsil whirlimixer. The tubes were then returned to the waterbath and left undisturbed for 48 hours before identification of the phase type using a crossed polarised viewer and an optical microscope. [Pg.244]

For these experiments, a binary mixture of sieved fractions of 150-250 pm (nominally 200 pm) and 710-840 pm (nominally 775 pm) glass beads was used. A symmetrical initial condition (top-to-bottom loading) is implemented. The blender is run at constant rotation rate a segregation pattern was assumed to be stable when it did not discernibly change for 100 revolutions. In many pharmaceutical operations, the mixing time is on the order of 100 500 revolutions, and experiments are run with regard to this timeframe. [Pg.174]

Successful liquid-phase separation on-chip was first carried out in CE, because EOF pumping can be easily achieved in the microscale. For instance, six fluorescein-labeled amino acids are separated by CE on a Pyrex glass chip (10-pm-deep and 30-pm-wide channel) (see Figure 6.5). Separation was achieved in a very short time of about 15 s [324]. Similar CE separation of calcein and fluorescein were also reported [582]. Separation of a binary mixture of rhodamine B and dichlorofluorescein was even achieved in only 0.8 ms using a short separation length of 200 pm [604]. [Pg.143]

Lennard-Jones binary mixture of particles is a prototypical model that describes glass-forming liquids [52,53,158,162-165]. The temperature and the density dependence of diffusivity D(T, p) have been obtained by computer simulations for the Lennard-Jones binary mixture in the supercooled state. To relate fragility of binary Lennard-Jones mixture to thermodynamic properties necessitates determination of the configurational entropy SC(T, p) as well as the vibration entropy Sv,h(T, p) at a given temperature and density. [Pg.94]

Figure 5.12 DTA traces of the base glass composition of particle size 125-250 /im, the ternary mixture soda ash-calcite-silica with a particle size of 90-125 fim, as well as various binary mixtures and soda ash alone from previous work [12]. All mixtures maintained the same relative percentages of constituents as those in the base glass batch. Figure 5.12 DTA traces of the base glass composition of particle size 125-250 /im, the ternary mixture soda ash-calcite-silica with a particle size of 90-125 fim, as well as various binary mixtures and soda ash alone from previous work [12]. All mixtures maintained the same relative percentages of constituents as those in the base glass batch.
The above result seems to adequately describe the observed Brillouin scattering of a homogeneous single-component-polymer fluid near its glass transition (13). If a binary mixture is truly homogeneous, then Equation 11 also should be valid for this case. However, if the two components phase separate, then the distribution function given by Equation 10 is invalid and further analysis is required. [Pg.523]

Figure 55. 2H NMR spectra for type B glasses at 777), ss 0.85. Results for the neat systems lolucncw/,. polybinadiene-7,. and decaline-7,s are shown together with those for the binary mixtures 45% chlorobenzene-<7 in decaline and 55% decalincw/, s in chlorobenzene. Solid-echo delays... Figure 55. 2H NMR spectra for type B glasses at 777), ss 0.85. Results for the neat systems lolucncw/,. polybinadiene-7,. and decaline-7,s are shown together with those for the binary mixtures 45% chlorobenzene-<7 in decaline and 55% decalincw/, s in chlorobenzene. Solid-echo delays...
In an examination of glass beads sieved into five fractions in the size range 70 to 400 mm it was found that the accuracy of the determined medians was good. The distribution widths and the resolution of binary mixtures were compared with image analysis. These showed some discrepancies for both mono-and bi-modal distributions with undersizing in both cases [166]. [Pg.563]

On the other hand, actual binary mixture tests using porous alumina and glass membranes show separation factor values for helium recovery from oxygen that are lower than what Knudsen diffusion provides, as indicated in Table 7.15. Only Koresh and Soffer [1983a 1983b] show an ideal separation factor of 20 to 40 with a low permeability of 1.2x10 barrers when molecular sieve membranes with a reported pore diameter of 0.3 to 0.5 nm are used. [Pg.282]

Crystal nucleation from the melt is but one type of nucleation in the condensed phase. Other processes of interest include the nucleation of salt crystals from aqueous solution, of one crystalline phase from another or from a glass, and of liquid crystal phases from one another or from the isotropic liquid. In this review we discuss only the nucleation of crystals from the melt. The major emphasis will be on single-component systems, although crystallization of alloys and binary mixtures will also be considered. [Pg.264]

One important point we should stress, in conjunction with our current interest, is that similar slow relaxation as liquid water is observed in much simpler model systems The binary mixture of Lennard-Jones liquids, which consist of two species of particles, is now studied extensively as a toy model of glass-forming liquids. It is simulated after careful preparation of simulation conditions to avoid crystallization. Also, the modified Lennard-Jones model glass, in which a many-body interaction potential is added to the standard pairwise Lennard-Jones potential, is also studied as a model system satisfying desired features. [Pg.392]

Fig. 1. Generation of model porous glasses using quench MD simulation of a binary mixture with a mole fraction ot 0.70. Quenching produces a series of phase-separated structures, which may be converted at any time into a porous network (shown in cutaway view at the bottom) by removing the component with the smaller mole fraction [25]. Fig. 1. Generation of model porous glasses using quench MD simulation of a binary mixture with a mole fraction ot 0.70. Quenching produces a series of phase-separated structures, which may be converted at any time into a porous network (shown in cutaway view at the bottom) by removing the component with the smaller mole fraction [25].
The glass-formers include molecular liquids and amorphous polymers of diverse chemical structures, room temperature ionic liquids, and binary mixtures of two van der Waals liquids" or two amorphous polymers. All show the property of temperature-pressure superpositioning of the frequency dispersion of the structural cr-relaxation at constant r . [Pg.8]

Keywords glass Uansition, pressure, stmctural relaxation, secondary relaxation, inter-molecular relaxation, binary mixtures... [Pg.40]

Binary mixtures of styrene oligomers with polar aromatic molecules have very good glass-forming and mixing properties. They are ideal systems for investigating selective dynamics of the polar component by dielectric... [Pg.42]

In ref. ( °) the applications of the analogous dependences (eq. (1) and (2)) for the pressure evolution of the glass temperature and the melting temperature in supercooled liquids were shown. It is noteworthy that both alcohols and water are important technological agents, also used as additives to the CO2 basic critical system. For the discussed case of binary mixtures of limited miscibility the critical behavior is the inherent feature of the system containing water and alcohol or nitrobenzene or nitrotoluene and alkanes, even under atmospheric pressure. When critical binary mixtures are considered as the base for the SCF technologies, no additional component is needed. [Pg.174]

Bending beam theory calculation of elastic modulus, 361-362 calculation of glass temperature, 362 calculation of thermal expansion coefficient, 362 layer stress determination, 361 Benzophenone-3,3, 4,4 -tetracarboxydi-anhydride-oxydianiline-m-phenylenediamine (BTDA-ODA-MPDA) polyimide, properties, 115-116 Bilayer beam analysis schematic representation of apparatus, 346,348/ thermal stress, 346 Binary mixtures of polyamic acids curing, 116-124 exchange reactions, 115 Bis(benzocyclobutenes) heat evolved during polymerization vs. [Pg.477]


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