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    Science opportunities from the Topex/Poseidon mission

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    The U.S. National Aeronautics and Space Administration (NASA) and the French Centre National d'Etudes Spatiales (CNES) propose to conduct a Topex/Poseidon Mission for studying the global ocean circulation from space. The mission will use the techniques of satellite altimetry to make precise and accurate measurements of sea level for several years. The measurements will then be used by Principal Investigators (selected by NASA and CNES) and by the wider oceanographic community working closely with large international programs for observing the Earth, on studies leading to an improved understanding of global ocean dynamics and the interaction of the ocean with other processes influencing life on Earth. The major elements of the mission include a satellite carrrying an altimetric system for measuring the height of the satellite above the sea surface; a precision orbit determination system for referring the altimetric measurements to geodetic coordinates; a data analysis and distribution system for processing the satellite data, verifying their accuracy, and making them available to the scientific community; and a principal investigator program for scientific studies based on the satellite observations. This document describes the satellite, its sensors, its orbit, the data analysis system, and plans for verifying and distributing the data. It then discusses the expected accuracy of the satellite's measurements and their usefulness to oceanographic, geophysical, and other scientific studies. Finally, it outlines the relationship of the Topex/Poseidon mission to other large programs, including the World Climate Research Program, the U.S. Navy's Remote Ocean Sensing System satellite program and the European Space Agency's ERS-1 satellite program

    Calibration of the Pulsed Electroacoustic Technique in the Presence of Trapped Charge

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    The influence of pulse voltage on the accuracy of charge density distribution in the pulsed electroacoustic technique (PEA) is discussed. It is shown that significant error can be introduced if a low dc voltage and high pulse voltage are used to calibrate charge density. However, our main focus in the present paper is to deal with one of the practical situations where space charge exists in the material prior to any measurements. The conventional calibration method can no longer be used to calibrate charge density due to the interference by the charge on the electrode induced by space charge. A method has been proposed which is based on two measurements. Firstly, the sample containing charge is measured without any applied voltage. The second measurement is carried out with a small external applied voltage. The applied voltage should be small enough so there is no disturbance of the existing charge in the sample. The difference of the two measurements can be used for calibration. An additional advantage of the proposed method avoids the influence of the pulse voltage on calibration and therefore gives a more accurate representation of space charge. The proposed method has been validated

    Potential distribution surrounding a photo- emitting plate in a dilute plasma

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    Potential distribution in photo-emitting plate in dilute plasma

    Small angle neutron scattering contrast variation reveals heterogeneities of interactions in protein gels

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    The structure of model gluten protein gels prepared in ethanol/water is investigated by small angle X-ray (SAXS) and neutrons (SANS) scattering. We show that gluten gels display radically different SAXS and SANS profiles when the solvent is (at least partially) deuterated. The detailed analysis of the SANS signal as a function of the solvent deuteration demonstrates heterogeneities of sample deuteration at different length scales. The progressive exchange between the protons (H) of the proteins and the deuteriums (D) of the solvent is inhomogeneous and 60 nm large zones that are enriched in H are evidenced. In addition, at low protein concentration, in the sol state, solvent deuteration induces a liquid/liquid phase separation. Complementary biochemical and structure analyses show that the denser protein phase is more protonated and specifically enriched in glutenin, the polymeric fraction of gluten proteins. These findings suggest that the presence of H-rich zones in gluten gels would arise from the preferential interaction of glutenin polymers through a tight network of non-exchangeable intermolecular hydrogen bonds.Comment: Soft Matter, Royal Society of Chemistry, 201
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