Zinn und Antimon in Legierungen

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Quantitative measurements of micro- and macromixing in a stirred vessel using Planar Laser-Induced Fluorescence

The Planar Laser-Induced Fluorescence (PLIF) technique enables measurement of the local degree of deviation in an arbitrary plane inside the mixing vessel. This is achieved by injecting a mixture of an inert dye and a reacting fluorescent into the vessel. The inert dye serves as a tracer for the macromixing. The fluorescent characteristics of the reacting dye change while undergoing a fast chemical reaction with the vessel content and it therefore shows the micromixing indirectly. The concentration fields of the dyes are measured simultaneously. For that a laser beam is expanded into a thin light sheet which illuminates an arbitrary plane in the mixing vessel, exciting the fluorescent dye in this area. The emitted light is detected by a CCD-camera which is positioned vertical to the measurement plane. The fluorescent light passes through two optical filters which are suitable for separating the fluorescent light of the two dyes. The light is then projected on half of the camera chip each so that the same display window is detected twice, and thus the local concentration of the two dyes can be measured simultaneously. Low Reynolds number measurements are performed in a mixing vessel equipped with a Rushton turbine. The lamellar structure is clearly resolved. Areas of micromixing are detected by calculating the local degree of deviation from the concentration fields. These areas are mainly found in the boundary layer of the lamellas.     

Watching photoinduced chemistry and molecular energy flow in solution in real time

Energized molecules are the essential actors in chemical transformations in solution. As the rearrangement of bonds requires a movement of nuclei, vibrational energy is often the driving force for a reaction. Vibrational energy can be redistributed within the "hot" molecule, or relaxation can occur when molecules interact. Both processes govern the rates, pathways, and quantum yields of chemical transformations in solution. Unfortunately, energy transfer and the breaking, formation, and rearrangement of bonds take place on ultrafast timescales. This Review highlights experimental approaches for the direct, ultrafast measurement of photoinduced femtochemistry and energy flow in solution. In the first part of this Review, we summarize recent experiments on intra- and intermolecular energy transfer. The second part discusses photoinduced decomposition of large organic peroxides, which are used as initiators in free radical polymerization. The mechanisms and timescales of their decarboxylation determine the initial steps of polymerization and the microstructure of the polymer product.     

Die Trennung des Zinns von anderen Metallen, insbesondere die Bestimmung desselben durch F?llung Mit Cupferron

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Wasserzusatz

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