Search results for "THERMODYNAMICS"
showing 10 items of 2774 documents
Reverse electrodialysis heat engine for sustainable power production
2017
Abstract Reverse Electrodialysis Heat Engine (REDHE) is a promising technology to convert waste heat at temperatures lower than 100 °C into electric power. In the present work an overview of the possible regeneration methods is presented and the technological challenges for the development of the RED Heat Engine (REDHE) are identified. The potential of this power production cycle was investigated through a simplified mathematical model. In the first part of the work, several salts were singularly modelled as possible solutes in aqueous solutions feeding the RED unit and the corresponding optimal conditions were recognized via an optimization study. In the second part, three different RED He…
Phase behavior of aqueous solutions of bovine serum albumin in the presence of dextran, at rest, and under shear.
2006
The demixing conditions for aqueous solutions of bovine serum albumin (BSA, fraction V) and for joint solutions of BSA plus dextran (DEX, M(w) = 2000 kg/mol) were determined by turbidimetric measurements as a function of composition, temperature, and shear rate. Aqueous solutions of BSA phase separate upon heating. Within the region of BSA concentrations between 0.05 and 32 wt %, the demixing temperature, T1, falls from ca. 65 degrees C to an almost constant value of 45 degrees C. Adding DEX to the BSA solutions reduces the homogeneous region of the mixture drastically where the amount of DEX required to lower T1 to 25 degrees C decreases rapidly as the concentration of BSA is raised. Exper…
Complex miscibility behaviour for polymer blends in flow
1995
Abstract Experimental observations of the effect of shear flow on the miscibility of binary polymer blends are compared to calculations based on a generalized Gibbs energy of mixing Gγ˙. This mixing free energy characterizes the steady state established at shear rateγ˙, as the sum of G z , the equilibrium Gibbs energy and E s , the energy the system stores while flowing.
Pressure Effects on the Thermodynamics oftrans-Decahydronaphthalene/Polystyrene Polymer Solutions: Application of the Sanchez-Lacombe Lattice Fluid T…
2003
The cloud-point temperatures (T-cl's) of trans-decahydronaphthalene(TD)/polystyrene (PS, (M) over bar (w) = 270 000) solutions were determined by light scattering measurements over a range of temperatures (1-16degreesC), pressures (100-900 bar), and compositions (4.2-21.6 vol.-% polymer). The system phase separates upon cooling and T-cl was found to increase with rising pressure for constant composition. In the absence of special effects, this finding indicates positive excess volume for the mixing. Special attention was paid to the demixing temperatures as a function of pressure for different polymer solutions and the plots in the T-phi plane (where phi signifies volume fractions). The clo…
Shear influence on the phase separation of oligomer blends
1994
Shear influences on the phase separation behaviour of four different blends of ethylene glycol/propylene glycol oligomers, exhibiting upper critical solution temperatures, were investigated. Cloud point curves at rest (turbidity measurements) are reported for all systems, spinodal conditions (light scattering) and tie-lines (analysis of the coexisting phases) are given for some examples. Phase diagrams under shear were obtained from rheological data. They demonstrate that the demixing temperatures of systems where both glycols bear OH end-groups are lowered up to ca. 1°C by shear rates of 1000s−1; the critical composition, generalized to the non-equilibrium conditions of flow, is markedly s…
Surfactant Association: Recent Theoretical and Experimental Developments
1991
A theoretical model describing the association of ionic surfactants into rod-shaped micelles is combined with an approximate formula for the viscosity increase induced by rod-shaped aggregates. It is shown that most of the thermodynamic parameters of the association model can be obtained from viscosity measurements. The approach is applied to micellar solutions of hexadecylpyridinium salts. The pronounced effect of counter-ion concentration on the growth of rod-shaped micelles can be attributed to a slightly higher degree of counter-ion association in the cylindrical part than in the end portions. An attempt is made to explain the finding that the degree of counter-ion association is virtua…
On the Role of Drop Break Up for Coalescence Processes and Morphology Development in Polymer Blends under Shear
2005
Drop sizes and drop-size distributions were determined as a function of time at constant shear rates, γ, by means of an optical shear cell in combination with an optical light microscope after preshearing the samples at high γ. The systems under investigation were PIB 3/PDMS 152 (PIB: polyisobutylene, PDMS: poly(dimethylsiloxane), numbers: average molar masses in kg/mol) and COP 26*/PDMS 48 (COP: poly(dimethyl-co-methylphenylsiloxane), asterisk: apparent molar mass); all measurements refer to 25 °C. Systems and conditions were chosen such that shear rates in the vicinity of the intersection of the coalescence and the break up curves become experimentally accessible. Under these conditi…
An expansion–coalescence model to track gas bubble populations in magmas
2016
Abstract We propose a kinetic model that statistically describes the growth by decompression, exsolution and coalescence of a polydisperse population of gas bubbles in a silicate melt. The model is homogeneous in space and its main variable is a distribution function representing the probability to find a bubble of volume v and mass m at time t. The volume and mass growth rates are described by a simplification of the classical monodisperse bubble growth model. This simplification, which shortens computational time, removes the coupling between mass evolution and an advection–diffusion equation describing the behavior of the volatile concentration in the melt. We formulate three coalescence…
A new view on the kinetics of tricalcium silicate hydration
2016
Abstract C3S hydration is an interesting example of chemical coupling between C3S dissolution, C–S–H and portlandite precipitation. It occurs because Ca2 +, OH− and silicate ions are present in C3S, in both hydration products and in the surrounding solution. Various experimental data sets reveal that the undersaturation with respect to C3S always increases when C3S hydration enters into the deceleratory phase, leading to the conclusion that C3S dissolution is at the origin of this deceleration, not C–S–H growth. In addition, as soon as portlandite precipitates, the dissolution limits the hydration already in the acceleratory hydration step. The evolution of the undersaturation cannot accoun…
The effect of the internal architecture of polymer micronetwork colloids on the dynamics in highly concentrated dispersions
2007
Motivated by the finding that colloidal dispersions of polymer micronetwork spheres with a cross-link density of 1:50 (inverse number of monomer units between crosslinks) show significant deviations from the dynamics of hard spheres in the colloid glass as seen by dynamic light scattering (DLS) (E. Bartsch, V. Frenz, H. Sillescu J. Non — Cryst. Solids 172–174 (1994), 88–97), we have undertaken a systematic study of the effect of the crosslink density on the dynamics at high concentrations. Long-time self-diffusion coefficients D S L and collective diffusion coefficients D c were measured for colloids with crosslink densities of 1:10, 1:20 and 1:50 by forced Rayleigh scattering (FRS) and the…