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A sufficient condition for the two-nucleon interaction to produce a gaseous instability in the form of the appearance of inhomogeneous-spatial-density single-particle states of lower energy than the (homogeneous) plane-wave states is found to be simply that it gives binding in first order. The critical density at which the instability occurs thus signals the unambiguous breakdown of a plane-wave-based Hartree-Fock perturbation expansion for the ground state properties. Several examples are analysed. 相似文献
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Manuel Vásquez-Montoya Juan F.Montoya Daniel Ramirez Franklin Jaramillo 《Journal of Energy Chemistry》2021,(6):386-391
Upscaling perovskite solar cell fabrication is one of the key challenges in the pathway for commercialization.The slow evaporation of frequently used solvents (... 相似文献
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Balbina P. García-Aguilar Antonio Avalos Ramirez J. Peter Jones Michèle Heitz 《Chemical Papers》2011,65(3):373-379
The emissions of methane (CH4), a powerful greenhouse gas (GES), contribute to the increase in GES concentration level in the atmosphere. For this reason,
the importance of controlling CH4 emissions of anthropogenic origin has increased over the last decades. Physicochemical and biological processes are available
for treating CH4. For this reason, such properties as the solubility of CH4 in aqueous solutions and organic solvents are of great relevance in different applications in environmental engineering and
biotechnology. In this study, the solubility of CH4 was determined at 298 K and 101.3 kPa in organic solvents, such as polyoxyethylenesorbates (Tween 20, Tween 40, and Tween
60), and linear alcohols (methanol, ethanol, and butan-1-ol) alone and in their admixtures. Admixtures of methanol with butan-1-ol
exhibited the highest solubility of CH4, of around 0.49 g m−3 of solvent, whereas the solubility of CH4 in linear alcohols varied from 0.167 g m−3 to 0.41 g m−3 of solvent. In the case of Tweens, CH4 solubility decreased with the hydrophilic-lipophilic balance (HLB) number. 相似文献
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Braulio Aranda Sergio A. Moya Andres Vega Gonzalo Valdebenito Sofia Ramirez‐Lopez Pedro Aguirre 《应用有机金属化学》2019,33(4)
Aminocarbonylation of aryl halides, homogeneously catalysed by palladium, is an efficient method that can be employed for obtaining amides for pharmaceutical and synthetic applications. In this work, palladium (II) complexes containing P^N ligands were studied as catalysts in the aminocarbonylation of iodobenzene in the presence of diethylamine. Two types of systems were used: a palladium (II) complex formed in situ; and one prepared prior to the catalytic reaction. In general, the palladium complexes studied achieved high conversions in an average reaction time of less than 2 hr, which is less than that for the standard system (Pd (II)/PPh3) used. The pre‐synthesized complexes were faster than their in situ counterparts, as the latter require an induction time to form the Pd/P^N species. The structure and electronic properties of the ligand P^N can influence both the activity and the selectivity of the reaction, stabilizing the acyl‐palladium intermediates formed in a better manner. 相似文献
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Dr. Adrian Ramirez Dr. Samy Ould-Chikh Dr. Lieven Gevers Dr. Abhishek Dutta Chowdhury Dr. Edy Abou-Hamad Dr. Antonio Aguilar-Tapia Prof. Jean-Louis Hazemann Dr. Nimer Wehbe Dr. Abdullah J. Al Abdulghani Dr. Sergey M. Kozlov Prof. Luigi Cavallo Prof. Jorge Gascon 《ChemCatChem》2019,11(12):2879-2886
The alarming atmospheric concentration and continuous emissions of carbon dioxide (CO2) require immediate action. As a result of advances in CO2 capture and sequestration technologies (generally involving point sources such as energy generation plants), large amounts of pure CO2 will soon be available. In addition to geological storage and other applications of the captured CO2, the development of technologies able to convert this carbon feedstock into commodity chemicals may pave the way towards a more sustainable economy. Here, we present a novel multifunctional catalyst consisting of Fe2O3 encapsulated in K2CO3 that can transform CO2 into olefins via a tandem mechanism. In contrast to traditional systems in Fischer-Tropsch reactions, we demonstrate that when dealing with CO2 conversion (in contrast to CO), very high K loadings are key to activate CO2 via the well-known ‘potassium carbonate mechanism’. The proposed catalytic process is demonstrated to be as productive as existing commercial processes based on synthesis gas while relying on economically and environmentally advantageous CO2 feedstock. 相似文献
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