University of Valencia

About: University of Valencia is a education organization based out in Valencia, Spain. It is known for research contribution in the topics: Population & Context (language use). The organization has 27096 authors who have published 65669 publications receiving 1765689 citations. The organization is also known as: Universitat de València & UV.

The Belle II Physics Book

Abstract: The Belle II detector will provide a major step forward in precision heavy flavor physics, quarkonium and exotic states, searches for dark sectors, and many other areas. The sensitivity to a large number of key observables can be improved by about an order of magnitude compared to the current measurements, and up to two orders in very clean search measurements. This increase in statistical precision arises not only due to the increased luminosity, but also from improved detector efficiency and precision for many channels. Many of the most interesting observables tend to have very small theoretical uncertainties that will therefore not limit the physics reach. This book has presented many new ideas for measurements, both to elucidate the nature of current anomalies seen in flavor, and to search for new phenomena in a plethora of observables that will become accessible with the Belle II dataset. The simulation used for the studiesinthis book was state ofthe artat the time, though weare learning a lot more about the experiment during the commissioning period. The detector is in operation, and working spectacularly well.

Surfactant‐Assisted Synthesis of Mesoporous Alumina Showing Continuously Adjustable Pore Sizes

Abstract: Porous materials displaying tailor-made pore sizes and shapes are particularly interesting in a great variety of real and potential applications where molecular recognition is needed, such as shape-selective catalysis, molecular sieving, and selective adsorption. Classically, apart from silica, materials most commonly used for catalysis and catalyst supports have been those based on high surface aluminas, owing to their thermal, chemical, and mechanical stability and their low cost. Earlier aluminas with high surface areas (~500 m/g) had been prepared using structure-directing agents. However, they were X-ray amorphous materials and their porosity was purely textural, characterized by wide pore size distributions. More recently, the discovery by researchers at Mobil of the M41S family of mesoporous silicas synthesized by using micellar aggregates as templates, has promoted considerable development in the synthesis of materials with uniform pores in the mesoporous range. However, in the case of mesoporous aluminum oxide, the usual strategies used in the synthesis of mesoporous silica have not always yielded satisfactory results and only a few papers have reported on surfactant-assisted synthesis of mesoporous alumina. Davis and co-workers have reported the preparation of aluminas with narrow pore size distributions by the use of anionic surfactants but their solids always have an approximately constant pore size (ca. 20 Š) that cannot be tailored by changing the surfactant length. Conversely, Pinnavaia and co-workers report the use of neutral polyethylene oxides as directing agents for the synthesis of mesoporous solids for which both the d spacing and the pore diameters increase as the surfactant size does. In both cases, the synthetic pathway is based on typical procedures originally used for mesoporous silicas: the variation of the micelle diameter is achieved by increasing the surfactant chain length and/or addition of hydrophobic organic molecules. However, the scarcity and diversity of the reported results suggest that there is still a long way to go to obtain real control of the synthetic procedures for the preparation of mesoporous aluminas. In this context, we show that self-assembling processes leading to the formation of mesoporous aluminas can be controlled by adequately balancing such processes and the hydrolysis and condensation reactions occurring at the inorganic phase. This method has allowed us to isolate for the first time mesoporous aluminum oxides using cationic surfactants and, what is more important, to tune their pore size by the sole adjustment of the molar ratio of the reactants. Thermally stable aluminas with different pore diameters, henceforth denoted as ICMUV-1, were synthesized using CTABr (cetyltrimethylammonium bromide) as surfactantdirecting agent in a water/TEA (triethanolamine) medium. A constant 2/1 Al/CTABr molar ratio was always used, and the pore size adjustment was achieved by changing the Al (or surfactant)/water/TEA molar ratio. A typical synthetic procedure is as follows: 1) A solution containing 0.4 g (10 mmol) of NaOH in 2 mL of water was added to 40 mL of TEA and heated at 120 C for 5 min to evaporate the water. Over this solution, 10.9 mL (40 mmol) of Al sec-butoxide was slowly added with stirring. The resulting clear solution was then heated at 150 C for 10 min (solution I). 2) 7.28 g (20 mmol) of CTABr was dissolved in 40 mL of water at 60 C (solution II). 3) Solution I was slowly added, with vigorous stirring, to solution II at 60 C, and the mixture was allowed to age for 72 h to give a white suspension. The aged solid was then filtered, washed with ethanol, and dried at 30 C. Finally, the assynthesized mesostructured composite was calcined for 5 h at 500 C under air atmosphere to favor surfactant decomposition, and a mesoporous solid with a pore size of 33 Š was obtained. Solids with different pore sizes have been obtained by adjusting the Al (or surfactant)/water/TEA molar ratio in the range from 2/111/15 to 2/195/4 (see Table 1). In all cases, the samples have high thermal stability, as measured by the permanence of their X-ray diffraction peak after heating at 900 C.

Observation of Long-Range Elliptic Azimuthal Anisotropies in s =13 and 2.76 TeV pp Collisions with the ATLAS Detector

Abstract: ATLAS has measured two-particle correlations as a function of relative azimuthal-angle, $\Delta \phi$, and pseudorapidity, $\Delta \eta$, in $\sqrt{s}$=13 and 2.76 TeV $pp$ collisions at the LHC using charged particles measured in the pseudorapidity interval $|\eta|$<2.5. The correlation functions evaluated in different intervals of measured charged-particle multiplicity show a multiplicity-dependent enhancement at $\Delta \phi \sim 0$ that extends over a wide range of $\Delta\eta$, which has been referred to as the "ridge". Per-trigger-particle yields, $Y(\Delta \phi)$, are measured over 2<$|\Delta\eta|$<5. For both collision energies, the $Y(\Delta \phi)$ distribution in all multiplicity intervals is found to be consistent with a linear combination of the per-trigger-particle yields measured in collisions with less than 20 reconstructed tracks, and a constant combinatoric contribution modulated by $\cos{(2\Delta \phi)}$. The fitted Fourier coefficient, $v_{2,2}$, exhibits factorization, suggesting that the ridge results from per-event $\cos{(2\phi)}$ modulation of the single-particle distribution with Fourier coefficients $v_2$. The $v_2$ values are presented as a function of multiplicity and transverse momentum. They are found to be approximately constant as a function of multiplicity and to have a $p_{\mathrm{T}}$ dependence similar to that measured in $p$+Pb and Pb+Pb collisions. The $v_2$ values in the 13 and 2.76 TeV data are consistent within uncertainties. These results suggest that the ridge in $pp$ collisions arises from the same or similar underlying physics as observed in $p$+Pb collisions, and that the dynamics responsible for the ridge has no strong $\sqrt{s}$ dependence.

Natural hybrids from Saccharomyces cerevisiae, Saccharomyces bayanus and Saccharomyces kudriavzevii in wine fermentations

Abstract: Several wine isolates of Saccharomyces were analysed for six molecular markers, five nuclear and one mitochondrial, and new natural interspecific hybrids were identified. The molecular characterization of these Saccharomyces hybrids was performed based on the restriction analysis of five nuclear genes ( CAT8 , CYR1 , GSY1 , MET6 and OPY1 , located in different chromosomes), the ribosomal region encompassing the 5.8S rRNA gene and the two internal transcribed spacers, and sequence analysis of the mitochondrial gene COX2 . This method allowed us to identify and characterize new hybrids between Saccharomyces cerevisiae and Saccharomyces kudriavzevii , between S. cerevisiae and Saccharomyces bayanus , as well as a triple hybrid S. bayanus × S. cerevisiae × S. kudriavzevii . This is the first time that S. cerevisiae × S. kudriavzevii hybrids have been described which have been involved in wine fermentation.