Study of shuttle imaging microwave system antenna. Volume 1: Conceptual design

A detailed preliminary design and complete performance evaluation are presented of an 11-channel large aperture scanning radiometer antenna for the shuttle imaging microwave system (SIMS) program. Provisions for interfacing the antenna with the space shuttle orbiter are presented and discussed. A program plan for hardware development and a rough order of magnitude (ROM) cost are also included. The conceptual design of the antenna is presented. It consists of a four-meter diameter parabolic torus main reflector, which is a graphite/epoxy shell supported by a graphite/epoxy truss. A rotating feed wheel assembly supports six Gregorian subreflectors covering the upper eight frequency channels from 6.6 GHz through 118.7 GHz, and two three-channel prime forms feed assemblies for 0.6, 1.4, and 2.7 GHz. The feed wheel assembly also holds the radiometers and power supplies, and a drive system using a 400 Hz synchronous motor is described. The RF analysis of the antenna is performed using physical optics procedures for both the dual reflector Gregorian concept and the single reflector prime focus concept. A unique aberration correcting feed for 2.7 GHz is analyzed. A structural analysis is also included. The analyses indicate that the antenna will meet system requirements

Selective Analysis of Redox Processes at the Electrode Interface with Time-Resolved Raman Spectroscopy

Electrochemistry and electrochemical reactions are increasingly important in the transition to a sustainable chemical industry. The electron transfer that drives such reactions takes place within nanometers of the electrode surface, and follow-up chemical reactions take place within the diffusion layer. Hence, understanding electrochemical reactions requires time-, potential-, and spatially resolved analysis. The confocal nature of Raman spectroscopy provides high spatial resolution, in addition to detailed information on molecular structure. The intrinsic weakness of nonresonant Raman scattering, however, is not sensitive enough for relatively minor changes to the solution resulting from reactions at the electrode interface. Indeed, the limit of detection is typically well above the concentrations used in electrochemical studies. Here, we show that surface-enhanced Raman scattering (SERS) and resonance Raman (rR) spectroscopy allow for spatially and time-resolved analysis of solution composition at (&lt;1-2 nm) and near (within 5 μm) the electrode surface, respectively, in a selective manner for species present at low (&lt;1 mM) concentrations. We show changes in concentration of species at the electrode surface, without the need for labels, specific adsorption, or resonance enhancement, using a SERS-active gold electrode prepared readily by electrochemical surface roughening. A combination of smooth and roughened gold electrodes is used to distinguish between surface and resonance enhancement using the well-known redox couples ferrocene and 2,2’-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS). We discuss the impact of specific adsorption on the spectral analysis with the ruthenium(II) polypyridyl complex, [Ru(bpy)3]2+. The dual function of the electrode (surface enhancement and electron transfer) in the analysis of solution processes is demonstrated with the reversible oxidation of TMA (4,N,N-trimethylaniline), where transient soluble species are identified in real time, with rapid spectral acquisition, making use of localized enhancement. We anticipate that this approach will find use in elucidating electro(catalytic) reactions at electrode interfaces.</p

Insect antifeedant and growth regulating activities of neem seed oil- the role of major tetranortriterpenoids

An attempt was made to correlate insect antifeedant and growth regulatory activities of neem (Azadirachta indica) seed oil with the major tetranortriterpenoids. Selective elimination of triterpenoids by preparative high-performance liquid chromatography, incorporation of the eliminated compounds in defined concentrations and bioassaying the resultant fractions against Spodoptera litura indicated the necessity to quantify major triterpenoids for correlation of bioactivity of neem oil

The contribution of mangrove expansion to salt marsh loss on the Texas Gulf coast

Landscape-level shifts in plant species distribution and abundance can fundamentally change the ecology of an ecosystem. Such shifts are occurring within mangrove-marsh ecotones, where over the last few decades, relatively mild winters have led to mangrove expansion into areas previously occupied by salt marsh plants. On the Texas (USA) coast of the western Gulf of Mexico, most cases of mangrove expansion have been documented within specific bays or watersheds. Based on this body of relatively small-scale work and broader global patterns of mangrove expansion, we hypothesized that there has been a recent regional-level displacement of salt marshes by mangroves. We classified Landsat-5 Thematic Mapper images using artificial neural networks to quantify black mangrove (Avicennia germinans) expansion and salt marsh (Spartina alterniflora and other grass and forb species) loss over 20 years across the entire Texas coast. Between 1990 and 2010, mangrove area grew by 16.1 km2, a 74% increase. Concurrently, salt marsh area decreased by 77.8 km2, a 24% net loss. Only 6% of that loss was attributable to mangrove expansion; most salt marsh was lost due to conversion to tidal flats or water, likely a result of relative sea level rise. Our research confirmed that mangroves are expanding and, in some instances, displacing salt marshes at certain locations. However, this shift is not widespread when analyzed at a larger, regional level. Rather, local, relative sea level rise was indirectly implicated as another important driver causing regional-level salt marsh loss. Climate change is expected to accelerate both sea level rise and mangrove expansion; these mechanisms are likely to interact synergistically and contribute to salt marsh loss.The open access fee for this work was funded through the Texas A&M University Open Access to Knowledge (OAK) Fund

pH-Induced Changes in the SERS Spectrum of Thiophenol at Gold Electrodes during Cyclic Voltammetry

Thiophenol is a model compound used in the study of self-assembly of arylthiols on gold surfaces. In particular, changes in the surface-enhanced Raman scattering (SERS) spectra of these self-assembled monolayers (SAMs) with a change of conditions have been ascribed to, for example, differences in orientation with respect to the surface, protonation state, and electrode potential. Here, we show that potential-induced changes in the SERS spectra of SAMs of thiophenol on electrochemically roughened gold surfaces can be due to local pH changes at the electrode. The changes observed during the potential step and cyclic voltammetry experiments are identical to those induced by acid–base switching experiments in a protic solvent. The data indicate that the potential-dependent spectral changes, assigned earlier to changes in molecular orientation with respect to the surface, can be ascribed to changes in the pH locally at the electrode. The pH at the electrode can change as much as several pH units during electrochemical measurements that reach positive potentials where oxidation of adventitious water can occur. Furthermore, once perturbed by applying positive potentials, the pH at the electrode takes considerable time to recover to that of the bulk solution. It is noted that the changes in pH even during cyclic voltammetry in organic solvents can be equivalent to the addition of strong acids, such as CF3SO3H, and such effects should be considered in the study of the redox chemistry of pH-sensitive redox systems and potential-dependent SERS in particular

Chelating Compounds and Immobilized Tethered Chelators

Novel di- and tripodal compounds useful as chelators, intermediates for their production and a method for treating an aqueous solution to remove trivalent metal ions are presented

Removing Aluminum from Solution Using Chelating Compounds and Immobilized Tethered Chelators

Methods are described for removing aluminum from a solution using novel di- and tripodal compounds as chelators

Micro-Water harvesting and soil amendment increase grain yields of barley on a Heavy-Textured alkaline sodic soil in a rainfed Mediterranean environment

This paper focuses on the adverse effects of soil sodicity and alkalinity on the growth of barley (Hordeum vulgare L.) in a rainfed environment in south-western Australia. These conditions cause the accumulation of salt (called ‘transient salinity’) in the root zone, which decreases the solute potential of the soil solution, particularly at the end of the growing season as the soil dries. We hypothesized that two approaches could help overcome this stress: (a) improved micro-water harvesting at the soil surface, which would help maintain soil hydration, decreasing the salinity of the soil solution, and (b) soil amelioration using small amounts of gypsum, elemental sulfur or gypsum plus elemental sulfur, which would ensure greater salt leaching. In our experiments, improved micro-water harvesting was achieved using a tillage technique consisting of exaggerated mounds between furrows and the covering of these mounds with plastic sheeting. The combination of the mounds and the application of a low rate of gypsum in the furrow (50 kg ha−1) increased yields of barley grain by 70% in 2019 and by 57% in 2020, relative to a control treatment with conventional tillage, no plastic sheeting and no amendment. These increases in yield were related to changes in ion concentrations in the soil and to changes in apparent electrical conductivity measured with the EM3

Risk Assessment Plan for Petroleum Underground Storage Tanks in Kentucky, Part ll: Diesel, Heating Oil, Other Middle Distillates and Waste Oil

This report consists of an appendix :Risk Assessment Plan for Petroleum Underground Storage Tanks in Kentucky and a second appendix: Environmental Half-Life and Ecological Effects of PAH

Chelating Compounds and Immobilized Tethered Chelators

Novel compounds useful as chelators, intermediates for their production and methods for removing trivalent and tetravalent metal ions from solution are presented.https://irl.umsl.edu/patents/1063/thumbnail.jp