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- ItemLas Pailas geothermal field - Central America case study: Deciphering a volcanic geothermal play type through the combination of optimized geophysical exploration methods and classic geological conceptual models of volcano-tectonic systems(London [u.a.] : Institute of Physics, 2019) Salguero, Leonardo SolÃs; Rioseco, Ernesto MenesesSustainable exploitation strategies of high-enthalpy geothermal reservoirs in a volcanic geothermal play type require an accurate understanding of key geological structures such as faults, cap rock and caldera boundaries. Of same importance is the recognition of possible magmatic body intrusions and their morphology, whether they are tabular like dikes, layered like sills or domes. The relative value of those magmatic bodies, their age, shape and location rely on the role they play as possible local heat sources, hydraulic barriers between reservoir compartments, and their far-reaching effect on the geochemistry and dynamics of fluids. Obtaining detailed knowledge and a more complete understanding at the early stages of exploration through integrated geological, geophysical and geochemical methods is essential to determine promising geothermal drilling targets for optimized production/re-injection schemes and for the development of adequate exploitation programs. Valuable, extensive geophysical data gathered at Las Pailas high-enthalpy geothermal field at northwestern Costa Rica combined with detailed understanding of the geological structures in the underground may represent a sound basis for an in-depth geoscientific discussion on this topic. Currently, the German cooperation for the identification of geothermal resources in Central America, implemented by the Federal Institute for Geosciences and Natural Resources (BGR), supports an international and interdisciplinary effort, driven by the Instituto Costarricense de Electricidad (ICE) with different international and national research institutions, including the Leibniz Institute for Applied Geophysics (LIAG). The discussions and joint studies refer to the optimized utilization of geophysical and geological methods for geothermal exploration in the Central American region, using the example of Las Pailas Geothermal Field. The results should contribute to a better understanding of the most appropriate geothermal exploration concepts for complex volcanic field settings in Central America.
- ItemThe Contrasting Character of Early and Late Transition Metal Fluorides as Hydrogen Bond Acceptors(Washington, DC : ACS Publications, 2015) Smith, Dan A.; Beweries, Torsten; Blasius, Clemens; Jasim, Naseralla; Nazir, Ruqia; Nazir, Sadia; Robertson, Craig C.; Whitwood, Adrian C.; Hunter, Christopher A.; Brammer, Lee; Perutz, Robin N.The association constants and enthalpies for the binding of hydrogen bond donors to group 10 transition metal complexes featuring a single fluoride ligand (trans-[Ni(F)(2-C5NF4)(PR3)2], R = Et 1a, Cy 1b, trans-[Pd(F)(4-C5NF4)(PCy3)2] 2, trans-[Pt(F){2-C5NF2H(CF3)}(PCy3)2] 3 and of group 4 difluorides (Cp2MF2, M = Ti 4a, Zr 5a, Hf 6a; Cp*2MF2, M = Ti 4b, Zr 5b, Hf 6b) are reported. These measurements allow placement of these fluoride ligands on the scales of organic H-bond acceptor strength. The H-bond acceptor capability β (Hunter scale) for the group 10 metal fluorides is far greater (1a 12.1, 1b 9.7, 2 11.6, 3 11.0) than that for group 4 metal fluorides (4a 5.8, 5a 4.7, 6a 4.7, 4b 6.9, 5b 5.6, 6b 5.4), demonstrating that the group 10 fluorides are comparable to the strongest organic H-bond acceptors, such as Me3NO, whereas group 4 fluorides fall in the same range as N-bases aniline through pyridine. Additionally, the measurement of the binding enthalpy of 4-fluorophenol to 1a in carbon tetrachloride (−23.5 ± 0.3 kJ mol–1) interlocks our study with Laurence’s scale of H-bond basicity of organic molecules. The much greater polarity of group 10 metal fluorides than that of the group 4 metal fluorides is consistent with the importance of pπ–dπ bonding in the latter. The polarity of the group 10 metal fluorides indicates their potential as building blocks for hydrogen-bonded assemblies. The synthesis of trans-[Ni(F){2-C5NF3(NH2)}(PEt3)2], which exhibits an extended chain structure assembled by hydrogen bonds between the amine and metal-fluoride groups, confirms this hypothesis.
- ItemPP/SWCNT composites modified with ionic liquid(Melville, NY : AIP, 2017) Krause, Beate; Predtechenskiy, M.; Ilin, E.; Pötschke, PetraPolypropylene composites filled with singlewalled carbon nanotubes TUBALL® (SWCNTs) were studied with regard to the effect of ionic liquid (IL) addition in different SWCNT:IL ratios (1:0.5 - 1:6). The incorporation of IL leads to a decrease of the electrical percolation threshold and already at 0.025 wt% SWCNT loading reduced resistivity values can be observed. However, the SWCNT macro dispersion, already relatively good without IL, was not affected by the IL incorporation. In addition, the nucleation effect of the SWCNT in polypropylene is not influenced when simultaneously adding IL, whereas the crystallization enthalpy slightly decreases with its addition.