Correlations of a bound interface over a random substrate

The correlation function of a one-dimensional interface over a random substrate, bound to the substrate by a pressure term, is studied by Monte-Carlo simulation. It is found that the height correlation , averaged over the substrate disorder, fits a form exp(-(j/b)^c) to a surprising precision in the full range of j where the correlation is non-negligible. The exponent c increases from 1.0 to 1.5 when the interface tension is taken larger and larger.Comment: 7 pages, 5 figure

Dynamics of Spreading of Chainlike Molecules with Asymmetric Surface Interactions

In this work we study the spreading dynamics of tiny liquid droplets on solid surfaces in the case where the ends of the molecules feel different interactions with respect to the surface. We consider a simple model of dimers and short chainlike molecules that cannot form chemical bonds with the surface. We use constant temperature Molecular Dynamics techniques to examine in detail the microscopic structure of the time dependent precursor film. We find that in some cases it can exhibit a high degree of local order that can persist even for flexible chains. Our model also reproduces the experimentally observed early and late-time spreading regimes where the radius of the film grows proportional to the square root of time. The ratios of the associated transport coefficients are in good overall agreement with experiments. Our density profiles are also in good agreement with measurements on the spreading of molecules on hydrophobic surfaces.Comment: 12 pages, LaTeX with APS macros, 21 figures available by contacting [email protected], to appear in Phys. Rev.

Dewetting, partial wetting and spreading of a two-dimensional monolayer on solid surface

We study the behavior of a semi-infinite monolayer, which is placed initially on a half of an infinite in both directions, ideal crystalline surface, and then evolves in time due to random motion of the monolayer particles. Particles dynamics is modeled as the Kawasaki particle-vacancy exchange process in the presence of long-range attractive particle-particle interactions. In terms of an analytically solvable mean-field-type approximation we calculate the mean displacement X(t) of the monolayer edge and discuss the conditions under which such a monolayer spreads (X(t) > 0), partially wets (X(t) = 0) or dewets from the solid surface (X(t) < 0).Comment: 4 pages, 2 figures, to appear in PRE (RC

Spreading of a Macroscopic Lattice Gas

We present a simple mechanical model for dynamic wetting phenomena. Metallic balls spread along a periodically corrugated surface simulating molecules of liquid advancing along a solid substrate. A vertical stack of balls mimics a liquid droplet. Stochastic motion of the balls, driven by mechanical vibration of the corrugated surface, induces diffusional motion. Simple theoretical estimates are introduced and agree with the results of the analog experiments, with numerical simulation, and with experimental data for microscopic spreading dynamics.Comment: 19 pages, LaTeX, 9 Postscript figures, to be published in Phy. Rev. E (September,1966

Force-velocity relation and density profiles for biased diffusion in an adsorbed monolayer

In this paper, which completes our earlier short publication [Phys. Rev. Lett. 84, 511 (2000)], we study dynamics of a hard-core tracer particle (TP) performing a biased random walk in an adsorbed monolayer, composed of mobile hard-core particles undergoing continuous exchanges with a vapor phase. In terms of an approximate approach, based on the decoupling of the third-order correlation functions, we obtain the density profiles of the monolayer particles around the TP and derive the force-velocity relation, determining the TP terminal velocity, V_{tr}, as the function of the magnitude of external bias and other system's parameters. Asymptotic forms of the monolayer particles density profiles at large separations from the TP, and behavior of V_{tr} in the limit of small external bias are found explicitly.Comment: Latex, 31 pages, 3 figure

Dynamics of liquid He-4 in confined geometries from Time-Dependent Density Functional calculations

We present numerical results obtained from Time-Dependent Density Functional calculations of the dynamics of liquid He-4 in different environments characterized by geometrical confinement. The time-dependent density profile and velocity field of He-4 are obtained by means of direct numerical integration of the non-linear Schrodinger equation associated with a phenomenological energy functional which describes accurately both the static and dynamic properties of bulk liquid He-4. Our implementation allows for a general solution in 3-D (i.e. no symmetries are assumed in order to simplify the calculations). We apply our method to study the real-time dynamics of pure and alkali-doped clusters, of a monolayer film on a weakly attractive surface and a nano-droplet spreading on a solid surface.Comment: q 1 tex file + 9 Ps figure

Challenges and opportunities of achieving European CO₂ transportation and storage specifications for carbon capture in the iron and steel industry

The application of CCS in the iron and steel industry faces particular challenges for achieving European CO2 transportation and storage in meeting CO₂ stream impurity limit specifications due to the unique and diverse composition of the steelworks off-gases targeted for CO₂ capture and the separation efficiency of proposed CO₂ capture solutions. This paper reviews the range and levels of compounds that could form potential CO₂ impurities in steelworks off-gases and provides estimates of the quality of CO₂ products obtained in primary CO₂ capture steps from Blast Furnace Gas (BFG) using different technologies of Pressure-Swing Adsorption (PSA) and amine scrubbing. Published CO₂ specifications from European transportation and storage operators are reviewed and compared. Additional suitable purification steps that are needed in order to reduce the levels of impurities from primary CO₂ product streams in order to achieve European CO₂ impurity limit specifications are identified, characterised and the associated cost implications discussed

Molecular ordering of precursor films during spreading of tiny liquid droplets

In this work we address a novel feature of spreading dynamics of tiny liquid droplets on solid surfaces, namely the case where the ends of the molecules feel different interactions to the surface. We consider a simple model of dimers and short chain--like molecules which cannot form chemical bonds with the surface. We study the spreading dynamics by Molecular Dynamics techniques. In particular, we examine the microscopic structure of the time--dependent precursor film and find that in some cases it can exhibit a high degree of local order. This order persists even for flexible chains. Our results suggest the possibility of extracting information about molecular interactions from the structure of the precursor film.Comment: 4 pages, revtex, no figures, complete file available from ftp://rock.helsinki.fi/pub/preprints/tft/ or at http://www.physics.helsinki.fi/tft/tft_preprints.html (to appear in Phys. Rev. E Rapid Comm.