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    Modelling carbon dynamics from urban land conversion: Fundamental model of city in relation to a local carbon cycle
    (London : Biomed Central, 2006) Svirejeva-Hopkins, A.; Schellnhuber, H.-J.
    Background: The main task is to estimate the qualitative and quantitative contribution of urban territories and precisely of the process of urbanization to the Global Carbon Cycle (GCC). Note that, on the contrary to many investigations that have considered direct anthropogenic emission of CO2(urbanized territories produce ca. 96-98% of it), we are interested in more subtle, and up until the present time, weaker processes associated with the conversion of the surrounding natural ecosystems and landscapes into urban lands. Such conversion inevitably takes place when cities are sprawling and additional "natural" lands are becoming "urbanized". Results: In order to fulfil this task, we first develop a fundamental model of urban space, since the type of land cover within a city makes a difference for a local carbon cycle. Hence, a city is sub-divided by built-up, "green"(parks, etc.) and informal settlements (favelas) fractions. Another aspect is a sub-division of the additional two regions, which makes the total number reaching eight regions, while the UN divides the world by six. Next, the basic model of the local carbon cycle for urbanized territories is built. We consider two processes: carbon emissions as a result of conversion of natural lands caused by urbanization; and the transformation of carbon flows by "urbanized" ecosystems; when carbon, accumulated by urban vegetation, is exported to the neighbouring territories. The total carbon flow in the model depends, in general, on two groups of parameters. The first includes the NPP, and the sum of living biomass and dead organic matter of ecosystems involved in the process of urbanization, and namely them we calculate here, using a new more realistic approach and taking into account the difference in regional cities' evolution. Conclusion: There is also another group of parameters, dealing with the areas of urban territories, and their annual increments. A method of dynamic forecasting of these parameters, based on the statistical regression model, was already suggested; nevertheless we shall further develop a new technique based on one idea to use the gamma-distribution. This will allow us to calculate the total carbon balance and to show how urbanization shifts it. © 2006 Svirejeva-Hopkins and Schellnhuber; licensee BioMed Central Ltd.
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    Oberflächenmorphologie von Arzneistoffpartikeln - Ein optisch evaluierbares Kriterium für die Auflösungsgeschwindigkeit
    (München : Elsevier, Urban & Fischer , 2002) Diebold, Steffen M.
    Für die Auflösungsgeschwindigkeit von schwer wasserlöslichen Arzneistoffpartikeln spielt die Hydrodynamik an den Partikel-Oberflächen eine große Rolle. Diese ist ihrerseits beeinflußt von der Geometrie und der Oberflächenmorphologie der Partikel. In dieser Arbeit wurde gezeigt, dass sich zur Charakterisierung dieser Parameter die Rasterelektronenmikroskopie (SEM) auch für die Untersuchung von Arzneistoffen gut eignet. Am Beispiel von Felodipin-Kristallen wurde nachgewiesen, dass reale Arzneistoffpulver auch an scheinbar „glatten“ Oberflächen Protrusionen, Kanten und Kavitäten aufweisen. Deren Größenordnungen lassen sich mit Hilfe der Elektronenmikroskopie abschätzen. Die Oberflächenmorphologie von Arzneistoffpartikeln ist ein Kriterium für die Auflösungsgeschwindigkeit oral verabreichter Arzneistoffe. Die Rasterelektronenmikroskopie leistet dabei wertvolle Dienste zur Charakterisierung der Oberflächen von Arzneistoffpartikeln.
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    Pyrimidine acyclo-C-nucleosides by ring transformations of 2-formyl-L-arabinal
    (Basel : MDPI, 2005) Bari, A.; Feist, H.; Michalik, M.; Peseke, K.
    The protected 2-formyl-L-arabinal 2 reacted with thiourea and cyanamide in the presence of sodium hydride to afford via ring transformations the 5-[1R,2S-1,2-bis(benzyloxy)-3-hydroxypropyl]-1,2-dihydropyrimidines 3 and 4, respectively. Similarly, treatment of 2 with 3-amino-2H-1,2,4-triazole yielded 6-[1R,25-1,2-bis(benzyloxy)-3-hydroxypropyl][1,2,4]-triazolo[1,5-a]pyrimidine(5) .
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    Comparison of the molecular properties and morphology of polypropylenes irradiated under different atmospheres and after annealing
    (Hoboken, NJ [u.a.] : Wiley InterScience, 2006) Krause, Beate; Häußler, Liane; Voigt, Dieter
    Electron-beam irradiation, a well-known way of generating long-chain branching, was used to modify polypropylene. Samples were investigated with differential scanning calorimetry, polarized light microscopy, and size exclusion chromatography. Independently of the atmosphere, postannealing led to the deactivation of residual radicals and to the reduction of the nucleus density. In comparison with the initial polypropylene, the crystallization temperatures increased for nonannealed samples but decreased for annealed samples. Stable products were obtained only by irradiation in nitrogen followed by annealing. A reaction including free radicals with oxygen in the ambient atmosphere led to increasing molar mass degradation and the formation of long-chain branching after Storage. © 2006 Wiley Periodicals, Inc.
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    Characterization of electron beam irradiated polypropylene: Influence of irradiation temperature on molecular and rheological properties
    (Hoboken, NJ [u.a.] : Wiley InterScience, 2006) Krause, Beate; Voigt, Dieter; Häuβler, Liane; Auhl, Dietmar; Münstedt, Helmut
    The aim of the investigations was to analyze the influence of the temperature during the irradiation process of polypropylene on the molar mass, the formation of long chain branching and the final branching topology. A linear isotactic polypropylene homopolymer was modified by electron beam irradiation at different temperatures, with two irradiation doses to insert long chain branching. The Samples were analyzed by size exclusion chromatography coupled with a multiangle laser light scattering detector, by differential scanning calorimetry, and by shear and elongational rheology. The shear and elongational flow behavior isdiscussed in terms of the influence of molecular parameters and used to analyze the topology of the irradiated samples. With increasing temperature, a slight reduction of the molar mass, an increase of long chain branching and an increase of crystallization temperature were found. © 2006 Wiley Periodicals, Inc.
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    An 8-fold parallel reactor system for combinatorial catalysis research
    (New York : Hindawi, 2006) Stoll, N.; Allwardt, A.; Dingerdissen, U.; Thurow, K.
    Increasing economic globalization and mounting time and cost pressure on the development of new raw materials for the chemical industry as well as materials and environmental engineering constantly raise the demands on technologies to be used. Parallelization, miniaturization, and automation are the main concepts involved in increasing the rate of chemical and biological experimentation. Copyright © 2006 Norbert Stoll et al.
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    Long-chain branching of polypropylene by electron-beam irradiation in the molten state
    (Hoboken, NJ [u.a.] : Wiley InterScience, 2006) Krause, Beate; Stephan, M.; Volkland, S.; Voigt, D.; Häußler, L.; Dorschner, H.
    The electron-beam irradiation of polymers generates modification effects in the macromolecular structure and material properties. Therefore, irradiation processing is mostly realized in the polymer solid state. In this way, the modification of linear polypropylene may result in long-chain branching of polypropylene macromolecules. The objective of this article is to investigate the effect of a polymer in the molten state during electron-beam irradiation on the macromolecular structure and material properties of polypropylene. For this procedure, a special irradiation vessel (BG3) has been developed in which a rapid transfer of polymer films from the solid state to the molten state and a defined temperature during electron-beam irradiation are realizable. The irradiated samples have been analyzed by high-temperature size exclusion chromatography coupled with a multi-angle laser light scattering detector and differential scanning calorimetry (DSC) measurements. With an increasing irradiation dose, a high reduction of the molar mass and an increasing amount of long-chain branching are found. Compared with irradiation in the solid state, the modification in the molten state leads to a higher degree of branching. The Theological experiments in elongation flow clearly exhibit the existence of long-chain branching. Furthermore, DSC measurements show that the glass-transition temperature and peak temperatures of melting and crystallization decrease. © 2005 Wiley Periodicals, Inc.
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    Nuevo sistema integrado cromatografía líquida de alta resolución / nebulizador hidráulico de alta presión y temperatura (HPLC/HT-HHPN) para la separación automática de la matriz en la determinación de metales en salmueras con espectrometría de absorción atómica (FAAS)
    (Sao Paulo : Scielo, 2000) Yáñez, J.; Berndt, H.
    An integrated HPF-system using HPLC and HT-HHP-nebulizer is used for matrix separation by the determination of heavy metals in highly concentrated solutions with FAAS. The separation of the matrix (NaCl) is achieved in a HPLC RP-C18 column after heavy metal complexing with trans-1,2-diaminciclohexane-N,N,N ,N -tetraacetic acid (CDTA). Matrix separation and the metal determination can be realized in less than one minute, without any interference from the matrix. The detection limits of Cd(II), Co(II), Cr(VI), Cu(II), Mn(II) and Zn(II) by FAAS were improved in one order of magnitude in compare with the direct determination by pneumatic nebulization nebulizer.
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    Local protonation control using plasmonic activation
    (Cambridge : RSC, 2001) Singh, P.; Deckert, V.
    Localized protonation of 4-mercaptopyridine (4-MPY), activated by light in the presence of silver nanoparticles is monitored under ambient conditions using surface-enhanced Raman scattering (SERS) and tip-enhanced Raman scattering (TERS). The reaction can be controlled by the excitation wavelength and the atmospheric conditions, thus, providing a tool for site-specific control of protonation.
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    Crystal structure of praseodym gallate, Pr4Ga2O9
    (München : R. Oldenbourg Verlag GmbH, 1999) Gesing, T.M.; Uecker, R.; Buhl, J.-C.
    Ga2O9Pr4, monoclinic, P121/c1 (No. 14), a = 7.8256(4) Å, b = 11.0322(5) Å, c = 11.4959(7) Å, β = 109.187(3)°, V = 937.4 Å3, Z = 4, R(P) = 0.026, wR(P) = 0.034, R(I)= 0.033, T = 295 K.