Surface roughening during plasma enhanced chemical vapor deposition of hydrogenated amorphous silicon on crystal silicon substrates.

The morphology of a series of thin films of hydrogenated amorphous silicon (a-Si:H) grown by plasma-enhanced chemical-vapor deposition (PECVD) is studied using scanning tunneling microscopy. The substrates were atomically flat, oxide-free, single-crystal silicon. Films were grown in a PECVD chamber directly connected to a surface analysis chamber with no air exposure between growth and measurement. The homogeneous roughness of the films increases with film thickness. The quantification of this roughening is achieved by calculation of both rms roughness and lateral correlation lengths of the a-Si:H film surface from the height difference correlation functions of the measured topographs. Homogeneous roughening occurs over the film surface due to the collective behavior of the flux of depositing radical species and their interactions with the growth surface

Nanoparticle deposition in hydrogenated amorphous silicon films during rf plasma deposition

Particles of 2–14 nm diameter, representing 10(– 4)–10(– 3) of the film volume, are observed by scanning tunneling microscopy (STM) in thin films of hydrogenated amorphous silicon (a-Si:H) grown by rf-plasma-enhanced deposition using optimized conditions. The particles are produced in the discharge and incorporated in the film during growth, in contradiction to expected particle trapping by discharge sheath fields. The interfaces between the nanoparticles and the homogeneous film can produce low-density regions that form electronic defects in a-Si:H films

Peruvian weapon system acquisition process

Historically, the acquisition of a weapon systems in the Republic of Peru has been made on the basis of system effectiveness and initial acquisition cost, with little or no consideration being given to operating and support costs that will be incurred after the system is deployed in the field. Peru acquires most of its sophisticated weapon systems from foreign countries. Under this situation, broad understanding of Life Cycle Cost (LCC) concept and techniques are needed. This thesis introduces the LCC concept, life cycle costing techniques and the methodology for Life Cycle Cost analysis in Peruvian Weapon Systems acquisition process. The research aims to show the effects that United Foreign Military Sales has in the Third World, the technology transfer as a decisive influence on the daily lives of most of the world population and the Soviet Union's arms trade with the Third World, the life cycle concept in Peruvian weapon acquisition process, and its fit into known economic analysis techniques.http://archive.org/details/peruviweaponsyst1094527579Colonel, Peruvian Air ForceApproved for public release; distribution is unlimited

Implants of polyanionic collagen matrix in bone defects of ovariectomized rats

In recent years, there has been a great interest in the development of biomaterials that could be used in the repair of bone defects. Collagen matrix (CM) has the advantage that it can be modified chemically to improve its mechanical properties. The aim of the present study was to evaluate the effect of three-dimensional membranes of native or anionic (submitted to alkaline treatment for 48 or 96 h) collagen matrix on the consolidation of osteoporosis bone fractures resulting from the gonadal hormone alterations caused by ovariectomy in rats subjected to hormone replacement therapy. The animals received the implants 4 months after ovariectomy and were sacrificed 8 weeks after implantation of the membranes into 4-mm wide bone defects created in the distal third of the femur with a surgical bur. Macroscopic analysis revealed the absence of pathological alterations in the implanted areas, suggesting that the material was biocompatible. Microscopic analysis showed a lower amount of bone ingrowth in the areas receiving the native membrane compared to the bone defects filled with the anionic membranes. In ovariectomized animals receiving anionic membranes, a delay in bone regeneration was observed mainly in animals not subjected to hormone replacement therapy. We conclude that anionic membranes treated with alkaline solution for 48 and 96 h presented better results in terms of bone ingrowth1913411348sem informaçãosem informaçã

Unsupported trimetallic Ni(Co)-Mo-W sulphide catalysts prepared from mixed oxides: characterisation and catalytic tests for simultaneous tetralin HDA and dibenzothiophene HDS reactions

Unsupported A-Mo-W (A = Ni or Co) sulphide catalysts were obtained from mixed oxides containing different W:Mo ratios. An in situ liquid-phase sulphidation of the mixed oxides in a batch reactor was followed by catalytic tests in a liquid-phase reaction (at 613 K and 70 bar), using a mixture of dibenzotiophene (DBT) and tetralin (THN) as the feed. After the catalytic tests, the bulk sulphide catalysts were characterised by nitrogen physical adsorption, XANES/EXAFS, SEM and HR-(S)TEM. The HR-TEM images showed randomly oriented, stacked-layer particles typical of Mo (W) sulphides and an elemental HR-STEM mapping evidenced Mo/W homogeneous distribution in the trimetallic sulphides. The EXAFS results for the trimetallic catalysts are consistent with the presence of nickel or cobalt sulphide domains, and Mo1-xWxS2 solid solutions. The intralayer Mo:W solid solutions were confirmed to be thermodynamically stable with respect to phase separation by DFT calculations, which were also used to aid in the interpretation of the EXAFS results. The effect of the W:Mo ratio on the catalytic properties of the Ni- and Co-containing series was found to be different. For the Ni series, increasing the W content caused an activity increase in THN hydrodearomatization (HDA) relative to DBT hydrodesulphurization (HDS), while it had little influence on the relative contribution of the direct desulphurisation (DDS) route with respect to the previous hydrogenation (HYD) route for DBT HDS. In contrast, for the Co series, the activities and selectivities were essentially insensitive to the W content. Both the Ni and Co series of unsupported sulphides were more selective for the HYD route in DBT HDS than a supported NiMo/Al2O3 catalyst

Atomic Charge Transfer-counter Polarization Effects Determine Infrared Ch Intensities Of Hydrocarbons: A Quantum Theory Of Atoms In Molecules Model.

Atomic charge transfer-counter polarization effects determine most of the infrared fundamental CH intensities of simple hydrocarbons, methane, ethylene, ethane, propyne, cyclopropane and allene. The quantum theory of atoms in molecules/charge-charge flux-dipole flux model predicted the values of 30 CH intensities ranging from 0 to 123 km mol(-1) with a root mean square (rms) error of only 4.2 km mol(-1) without including a specific equilibrium atomic charge term. Sums of the contributions from terms involving charge flux and/or dipole flux averaged 20.3 km mol(-1), about ten times larger than the average charge contribution of 2.0 km mol(-1). The only notable exceptions are the CH stretching and bending intensities of acetylene and two of the propyne vibrations for hydrogens bound to sp hybridized carbon atoms. Calculations were carried out at four quantum levels, MP2/6-311++G(3d,3p), MP2/cc-pVTZ, QCISD/6-311++G(3d,3p) and QCISD/cc-pVTZ. The results calculated at the QCISD level are the most accurate among the four with root mean square errors of 4.7 and 5.0 km mol(-1) for the 6-311++G(3d,3p) and cc-pVTZ basis sets. These values are close to the estimated aggregate experimental error of the hydrocarbon intensities, 4.0 km mol(-1). The atomic charge transfer-counter polarization effect is much larger than the charge effect for the results of all four quantum levels. Charge transfer-counter polarization effects are expected to also be important in vibrations of more polar molecules for which equilibrium charge contributions can be large.1623224-3

Stabilizing an Attractive Bose-Einstein Condensate by Driving a Surface Collective Mode

Bose-Einstein condensates of $^7$Li have been limited in number due to attractive interatomic interactions. Beyond this number, the condensate undergoes collective collapse. We study theoretically the effect of driving low-lying collective modes of the condensate by a weak asymmetric sinusoidally time-dependent field. We find that driving the radial breathing mode further destabilizes the condensate, while excitation of the quadrupolar surface mode causes the condensate to become more stable by imparting quasi-angular momentum to it. We show that a significantly larger number of atoms may occupy the condensate, which can then be sustained almost indefinitely. All effects are predicted to be clearly visible in experiments and efforts are under way for their experimental realization.Comment: 4 ReVTeX pages + 2 postscript figure