310 research outputs found
Recommended from our members
Re-entrant Appearance of Phases in a Relaxed Langmuir Monolayer of Tetracosanoic Acid as Determined by X-Ray Scattering
The structure of the fully relaxed phases of a Langmuir monolayer of tetracosanoic acid is determined by xâray diffraction and reflection along an isotherm at âź20.5â°C. Isotherms taken by allowing the surface pressure to stabilize between incremental compressions are seen to be qualitatively different from the constantârate nonrelaxed isotherms typically seen in the literature. At low densities the monolayer consists of an inhomogeneous film of islands of a crystalline (or hexatic) phase with molecular tilt ordering that is analogous to that of the smectic I liquid crystal. Small amounts of impurities (âź0.5% of the monolayer) account for the change in surface pressure with area in this region. Upon compression to the point that the free space between islands becomes negligible the film appears homogeneous. On further compression the time required for full relaxation becomes long (i.e., âź hours), the tilt angle of the molecular axis decreases and the xâray unit cell is compressed. Including this homogeneous I phase the phase sequence observed by diffraction upon compression is IâUâIâU, where U refers to an untilted orthorhombic phase. The outer two phases of this sequence are pure phases which form homogeneous monolayers, but the inner two are inhomogeneous phases each coexisting with an amorphous phase that does not have an observable diffraction signal. At the boundaries demarcating the I and U phases, a phase whose tilt ordering is analogous to that of a smectic F phase is seen to coexist. The preceding phase sequence is sensitive to the degree of relaxation permitted the monolayer after an incremental compression. In particular, if the monolayer is not allowed to relax completely after each compression, the untilted U phase may never appear. The UâI transition is shown to be reversible for a relaxed monolayer.Engineering and Applied Science
Activation of CD4 cells by fibronectin and anti-CD3 antibody. A synergistic effect mediated by the VLA-5 fibronectin receptor complex.
Chiral and herringbone symmetry breaking in water-surface monolayers
We report the observation from monolayers of eicosanoic acid in the Lâ˛2 phase of three distinct out-of-plane first-order diffraction peaks, indicating molecular tilt in a nonsymmetry direction and hence the absence of mirror symmetry. At lower pressures the molecules tilt in the direction of their nearest neighbors. In this region we find a structural transition, which we tentatively identify as the rotator-herringbone transition L2dâL2h
Recommended from our members
Thermal Diffuse X-Ray-Scattering Studies of the Water-Vapor Interface
Agreement between the theoretical and measured resolution dependence of x-ray specular reflection from the H2O-vapor interface shows that the macroscopic capillary model for surface roughness can be extended to length scales as small as 400 Ă
. Agreement between measured thermal diffuse scattering data and the theoretical form, with no significant adjustable parameters, independently leads to similar conclusions.Engineering and Applied Science
Recommended from our members
Relaxation and the Reentrant Appearance of Phases in a Molecular Monolayer
The structure of monolayers of on water, along 21C isotherms between 18 and 35 Ă
/molecule, has been studied with glancing-angle x-ray diffraction and specular reflection. Following an incremental area change, in some regions of the isotherm, the diffraction pattern evolves until the surface pressure is relaxing 0.01 dyn/cm h. Reentrant behavior between tilted and nontilted phases is observed. Phase coexistence is indicated by differences between the deposited area/molecule and the area of the x-ray-determined unit cell.Engineering and Applied Science
Recommended from our members
Gastric Bypass Surgery in Severely Obese Women With Type 1 Diabetes: Anthropometric and Cardiometabolic Effects at 1 and 5 Years Postsurgery: Table 1
VLA-4 mediates CD3-dependent CD4+ T cell activation via the CS1 alternatively spliced domain of fibronectin.
A critical assessment of methods for the intrinsic analysis of liquid interfaces. 1. surface site distributions
Substantial progress in our understanding of interfacial structure and dynamics has stemmed from the recent development of algorithms that allow for an intrinsic analysis of fluid interfaces. These work by identifying the instantaneous location of the interface, at the atomic level, for each molecular configuration and then computing properties relative to this location. Such a procedure eliminates the broadening of the interface caused by capillary waves and reveals the underlying features of the system. However, a precise definition of which molecules actually belong to the interfacial layer is difficult to achieve in practice. Furthermore, it is not known if the different intrinsic analysis methods are consistent with each other and yield similar results for the interfacial properties. In this paper, we carry out a systematic and detailed comparison of the available methods for intrinsic analysis of fluid interfaces, based on a molecular dynamics simulation of the interface between liquid water and carbon tetrachloride. We critically assess the advantages and shortcomings of each method, based on reliability, robustness, and speed of computation, and establish consistent criteria for determining which molecules belong to the surface layer. We believe this will significantly contribute to make intrinsic analysis methods widely and routinely applicable to interfacial systems
Nail lacquer filmsâ surface energies and in vitro water-resistance and adhesion do not predict their in vivo residence
The in vivo residence of nail lacquers (which are ideal topical drug carriers for the treatment of nail diseases) determines their frequency of application, and is thereby expected to influence patient adherence and success of treatment. Thus in vitro measurements to indicate lacquersâ in vivo residence are routinely conducted during formulation development. However the literature on in vitro-in vivo correlations is severely limited. Thus, the aim of the work discussed in this paper was to investigate correlations between in vivo residence and in vitro film resistance to water, in vitro film adhesion and surface energy of lacquer films. In vivo measurements were conducted on fingernails in six volunteers. Seven commercially available nail lacquers were tested in commonly-used measurements. Correlations between in vivo residence and in vitro water resistance and adhesion were found to be extremely poor. The surface energies of the lacquer films (which were between 33 and 39 mJ/m2) were also not predictive of in vivo residence. High density polyethylene (HDPE) sheet â whose surface energy was determined to be similar to that of the human nailplate â was found to be a suitable model for the nailplate (when investigating surface energy) and was used in a number of experiments
- âŚ