118 research outputs found
Surface Induced Order in Liquid Metals and Binary Alloys
Measurements of the surface x-ray scattering from several pure liquid metals
(Hg, Ga, and In) and from three alloys (Ga-Bi, Bi-In, and K-Na) with different
heteroatomic chemical interactions in the bulk phase are reviewed.
Surface-induced layering is found for each elemental liquid metal. The surface
structure of the K-Na alloy resembles that of an elemental liquid metal. Bi-In
displays pair formation at the surface. Surface segregation and a wetting film
are found for Ga-Bi.Comment: 10 pages, 3 fig, published in Journal of Physics: Condensed Matte
Microscopic Surface Structure of Liquid Alkali Metals
We report an x-ray scattering study of the microscopic structure of the
surface of a liquid alkali metal. The bulk liquid structure factor of the
eutectic K67Na33 alloy is characteristic of an ideal mixture, and so shares the
properties of an elemental liquid alkali metal. Analysis of off-specular
diffuse scattering and specular x-ray reflectivity shows that the surface
roughness of the K-Na alloy follows simple capillary wave behavior with a
surface structure factor indicative of surface induced layering. Comparison of
thelow-angle tail of the K67Na33 surface structure factor with the one measured
for liquid Ga and In previously suggests that layering is less pronounced in
alkali metals. Controlled exposure of the liquid to H2 and O2 gas does not
affect the surface structure, indicating that oxide and hydride are not stable
at the liquid surface under these experimental conditions.Comment: 12 pages, 3 figures, published in Phys. Rev.
Recommended from our members
Competition between Surface Layering and Surface Phase Formation in Dilute Liquid Hg−Au Alloys
We present temperature-dependent X-ray reflectivity measurements of liquid Hg alloyed with 0.06−0.20 atom % Au. At low Au concentrations, we find temperature-dependent surface-induced layering similar to that observed in pure Hg, except that the presence of Au reduces the layering amplitude. Upon approaching the solubility limit of Au in Hg, a new surface phase forms which is 1−2 atomic diameters thick and has a density of about half that of bulk Hg. We present a surface phase diagram, summarizing the evolution of this unexpected surface structure upon varying composition and temperature. Such surface modifications may account for the variations observed in catalytic and electrochemical reactions at liquid metal surfaces upon alloying.Engineering and Applied Science
Recommended from our members
Wetting Behavior at the Free Surface of a Liquid Gallium–Bismuth Alloy: An X-ray Reflectivity Study Close to the Bulk Monotectic Point
We present X-ray reflectivity measurements from the free surface of a liquid gallium–bismuth alloy (Ga–Bi) in the temperature range close to the bulk monotectic temperature =222C. Our measurements indicate a continuous formation of a thick wetting film at the free surface of the binary system driven by the first order transition in the bulk at the monotectic point. We show that the behavior observed is that of a complete wetting at a tetra point of solid–liquid–liquid–vapor coexistence.Engineering and Applied Science
Surface layering of liquids: The role of surface tension
Recent measurements show that the free surfaces of liquid metals and alloys
are always layered, regardless of composition and surface tension; a result
supported by three decades of simulations and theory. Recent theoretical work
claims, however, that at low enough temperatures the free surfaces of all
liquids should become layered, unless preempted by bulk freezing. Using x-ray
reflectivity and diffuse scattering measurements we show that there is no
observable surface-induced layering in water at T=298 K, thus highlighting a
fundamental difference between dielectric and metallic liquids. The
implications of this result for the question in the title are discussed.Comment: 5 pages, 4 figures, to appear in Phys. Rev. B. 69 (2004
Surface Structure of Liquid Metals and the Effect of Capillary Waves: X-ray Studies on Liquid Indium
We report x-ray reflectivity (XR) and small angle off-specular diffuse
scattering (DS) measurements from the surface of liquid Indium close to its
melting point of C. From the XR measurements we extract the surface
structure factor convolved with fluctuations in the height of the liquid
surface. We present a model to describe DS that takes into account the surface
structure factor, thermally excited capillary waves and the experimental
resolution. The experimentally determined DS follows this model with no
adjustable parameters, allowing the surface structure factor to be deconvolved
from the thermally excited height fluctuations. The resulting local electron
density profile displays exponentially decaying surface induced layering
similar to that previously reported for Ga and Hg. We compare the details of
the local electron density profiles of liquid In, which is a nearly free
electron metal, and liquid Ga, which is considerably more covalent and shows
directional bonding in the melt. The oscillatory density profiles have
comparable amplitudes in both metals, but surface layering decays over a length
scale of \AA for In and \AA for Ga. Upon controlled
exposure to oxygen, no oxide monolayer is formed on the liquid In surface,
unlike the passivating film formed on liquid Gallium.Comment: 9 pages, 5 figures; submitted to Phys. Rev.
Observation of surface layering in a nonmetallic liquid
Oscillatory density profiles (layers) have previously been observed at the
free surfaces of liquid metals, but not in other isotropic liquids. We have
used x-ray reflectivity to study a molecular liquid,
tetrakis(2-ethylhexoxy)silane. When cooled to T/Tc~0.25 (well above the
freezing point for this liquid), density oscillations appear at the surface.
Lateral order within the layers is liquid-like. Our results confirm theoretical
predictions that a surface-layered state will appear even in dielectric liquids
at sufficiently low temperatures, if not preempted by freezing.Comment: accepted for publication in Phys. Rev. Lett. 15 pages 4 figure
Pharmacokinetics of rifampicin in adult TB patients and healthy volunteers: a systematic review and meta-analysis
Objectives: The objectives of this study were to explore inter-study heterogeneity in the pharmacokinetics (PK)
of orally administered rifampicin, to derive summary estimates of rifampicin PK parameters at standard dosages
and to compare these with summary estimates for higher dosages.
Methods: A systematic search was performed for studies of rifampicin PK published in the English language up
to May 2017. Data describing the Cmax and AUC were extracted. Meta-analysis provided summary estimates
for PK parameter estimates at standard rifampicin dosages. Heterogeneity was assessed by estimation of the
I
2 statistic and visual inspection of forest plots. Summary AUC estimates at standard and higher dosages were
compared graphically and contextualized using preclinical pharmacodynamic (PD) data.
Results: Substantial heterogeneity in PK parameters was evident and upheld in meta-regression. Treatment
duration had a significant impact on the summary estimates for rifampicin PK parameters, with Cmax 8.98 mg/L
(SEM 2.19) after a single dose and 5.79 mg/L (SEM 2.14) at steady-state dosing, and AUC 72.56 mgh/L
(SEM 2.60) and 38.73 mgh/L (SEM 4.33) after single and steady-state dosing, respectively. Rifampicin dosages of
at least 25 mg/kg are required to achieve plasma PK/PD targets defined in preclinical studies.
Conclusions: Vast inter-study heterogeneity exists in rifampicin PK parameter estimates. This is not explained by
the available modifying variables. The recommended dosage of rifampicin should be increased to improve efficacy. This study provides an important point of reference for understanding rifampicin PK at standard dosages
as efforts to explore higher dosing strategies continue in this field
Microscopic View on Short-Range Wetting at the Free Surface of the Binary Metallic Liquid Gallium-Bismuth: An X-ray Reflectivity and Square Gradient Theory Study
We present an x-ray reflectivity study of wetting at the free surface of the
binary liquid metal gallium-bismuth (Ga-Bi) in the region where the bulk phase
separates into Bi-rich and Ga-rich liquid phases. The measurements reveal the
evolution of the microscopic structure of wetting films of the Bi-rich,
low-surface-tension phase along different paths in the bulk phase diagram. A
balance between the surface potential preferring the Bi-rich phase and the
gravitational potential which favors the Ga-rich phase at the surface pins the
interface of the two demixed liquid metallic phases close to the free surface.
This enables us to resolve it on an Angstrom level and to apply a mean-field,
square gradient model extended by thermally activated capillary waves as
dominant thermal fluctuations. The sole free parameter of the gradient model,
i.e. the so-called influence parameter, , is determined from our
measurements. Relying on a calculation of the liquid/liquid interfacial tension
that makes it possible to distinguish between intrinsic and capillary wave
contributions to the interfacial structure we estimate that fluctuations affect
the observed short-range, complete wetting phenomena only marginally. A
critical wetting transition that should be sensitive to thermal fluctuations
seems to be absent in this binary metallic alloy.Comment: RevTex4, twocolumn, 15 pages, 10 figure
The liquid-vapor interface of an ionic fluid
We investigate the liquid-vapor interface of the restricted primitive model
(RPM) for an ionic fluid using a density-functional approximation based on
correlation functions of the homogeneous fluid as obtained from the
mean-spherical approximation (MSA). In the limit of a homogeneous fluid our
approach yields the well-known MSA (energy) equation of state. The ionic
interfacial density profiles, which for the RPM are identical for both species,
have a shape similar to those of simple atomic fluids in that the decay towards
the bulk values is more rapid on the vapor side than on the liquid side. This
is the opposite asymmetry of the decay to that found in earlier calculations
for the RPM based on a square-gradient theory. The width of the interface is,
for a wide range of temperatures, approximately four times the second moment
correlation length of the liquid phase. We discuss the magnitude and
temperature dependence of the surface tension, and argue that for temperatures
near the triple point the ratio of the dimensionless surface tension and
critical temperature is much smaller for the RPM than for simple atomic fluids.Comment: 6 postscript figures, submitted to Phys. Rev.
- …