Symmetric electron-hole bilayer systems have been studied at zero temperature using the diffusion quantum Monte Carlo method. A flexible trial wave function is used that can describe fluid, excitonic, and biexcitonic phases. We calculate condensate fractions and pair correlation functions for a large number of densities r(s) and layer separations d. At small d we find a one-component fluid phas...

Equations of state should be tuned to reservoir conditions by PVT tests for phase behavior modeling. This tuning is achievable via an optimization method. In this work, simulated annealing algorithm is applied as a global optimization method to parameter optimization for PC-SAFT from the statistical associating fluid theory incorporating hard chain as reference fluid. The optimization parameter...

Starting with the Vlasov-Boltzmann equation for a binary fluid mixture, we derive an equation for the velocity field u when the system is segregated into two phases (at low temperatures) with a sharp interface between them. u satisfies the incompressible Navier-Stokes equations together with a jump boundary condition for the pressure across the interface which, in turn, moves with a velocity gi...

To study fluid-phase endocytosis in living cells and its relationship to changes in the cell cortex, we have used a green fluorescent protein (GFP)-tagged version of coronin, an actin-associated protein that localises to dynamic regions of the Dictyostelium cell cortex. In the confocal microscope, internalisation of fluorescently labelled dextran as a fluid-phase marker can be recorded simultan...

The fluid phase inactivation of C2(hu) by C1(hu) is markedly enhanced by the presence of C4(hu). The enhancement is afforded by C1 inactivated C4(hu), namely C4i(hu), and requires the simultaneous presence of enzymatically active C1. Heterologous C4 of guinea pig origin protects C2(hu) from the inactivation by C1(hu). Thus, in both the fluid phase and on the cellular intermediate, C4(hu) is ess...

Fluid-solid phase transition and coexistence of square-well fluids confined in narrow cylindrical hard pores are characterized using molecular simulation methods. The equation of state containing a fluid phase, a solid phase and a fluid-solid coexistence state was separately obtained for different attractive ranges of potential well and pore diameters; lambda=1.2, 1.3, 1.4, and 1.5 for a pore o...

The goal of accurately locating fluid phase boundaries by means of computer simulation is hampered by difficulties associated with sampling both coexisting phases in a single simulation. We explain the background to these difficulties and describe how they can be tackled using a synthesis of biased Monte Carlo sampling and histogram extrapolation methods, in conjunction with a standard fluid si...

The uptake of nutrients by plant cells has been traditionally believed to be mediated by membrane-bound carriers. However, the last decade has seen an increase in evidence pointing to the parallel uptake by fluid-phase endocytosis (FPE). Recent advances in plant endocytosis reveal that this is true for heterotrophic cells, whether storage parenchyma, cell suspensions, or nutrient absorbing cell...