18 research outputs found
Automatic Personalization of User Interfaces based on User Interaction Analytics
The default user interface (UI) of software applications is the same for all users, even though users differ in terms of their needs and preferences for using the software. UI customization is typically limited to the most advanced and/or highly active users. As a result, a significant proportion of users of a software do not reap the benefits of having a UI that is personalized to them. This disclosure describes techniques to determine and present a personalized UI to each user or an application, with the user’s permission. UI personalization is performed based on analytics of user-permitted data of user interaction and other relevant information. The analysis can be performed by a suitably trained machine learning model which outputs the optimal personalized UI for each user. Model training and execution is performed on the user device, and if the user permits, on a server that trains the model based on aggregated, non-identifiable user data
Measurement of the t(t)over-bar production cross section in pp collisions at root s=7 TeV in dilepton final states containing a tau
The top quark pair production cross section is measured in dilepton events with one electron or muon, and one hadronically decaying tau lepton from the decay t (t) over bar -> (l nu(l))((sic)(h)nu((sic)))b (b) over bar, (l = e, mu). The data sample corresponds to an integrated luminosity of 2.0 fb(-1) for the electron channel and 2.2 fb(-1) for the muon channel, collected by the CMS detector at the LHC. This is the first measurement of the t (t) over bar cross section explicitly including tau leptons in proton- proton collisions at root s = 7 TeV. The measured value sigma(t (t) over bar) = 143 +/- 14(stat) +/- 22(syst) +/- 3(lumi) pb is consistent with the standard model predictions
Choosing optimal rapid manufacturing process for thin-walled products using expert algorithm
Experimental Studies on 3D Printing of Automatically Designed Customized Wrist-Hand Orthoses
Mechanistic role of nitrate anion in TCE dechlorination by ball milled ZVI and sulfidated ZVI: Experimental investigation and theoretical analysis
Distinct Role of Long 3′ UTR BDNF mRNA in Spine Morphology and Synaptic Plasticity in Hippocampal Neurons
Adsorption isotherm, mechanism, and geometry of Pb(II) on magnetites substituted with transition metals
Competitive adsorption geometries for the arsenate As(V) and phosphate P(V) oxyanions on magnetite surfaces: Experiments and theory
In the present study, the competitive adsorption geometries for arsenate and phosphate on magnetite surfaces over a pH range of 4–9 were investigated using in situ attenuated total reflectance Fourier-transform infrared spectroscopy (ATR-FTIR) and two-dimensional correlation analysis (2D-COS). The adsorption energies and infrared vibrational frequencies of these surface complexes were also calculated by first-principles simulations. Arsenate and phosphate have different preferences for the magnetite surface in the presence of aqueous solvent at both acid and alkaline pH. For the adsorption of phosphate, mono-protonated monodentate mononuclear (MMM) complexes dominated at acid pH, while non-protonated bidentate binuclear (NBB) complexes were dominant at alkaline pH. Arsenate mainly formed bidentate binuclear (BB) complexes with some outer-sphere species, both of which were more prevalent at acid pH. The pre-absorbed inner-sphere arsenate species were scarcely affected by the introduction of phosphate. However, the pre-absorbed phosphate oxyanions, especially the MMM complexes, were significantly substituted by BB arsenate at the magnetite surfaces. The adsorption affinity of phosphate and arsenate species for magnetite surface was found to increase in the following order: MMM phosphate complex < NBB phosphate complex < BB arsenate complex, which was consistent with the calculated adsorption energies. The simulated infrared vibrational frequencies for the most favorable adsorption modes of each oxyanion display distinctive patterns, and their trends are in excellent agreement with experimental data.
The effects of pH, adsorption sequence, and mineral species on the competitive adsorption between arsenate and phosphate oxyanions are also discussed, and their different competing ability and stability on the magnetite surfaces can be ascribed to the variations in adsorption geometry and strength of binding. To the best of our knowledge, this is the first study aiming to distinguish the stability of the different phosphate and arsenate complexes on magnetite by employing a combined approach of in situ spectroscopy and DFT simulations. Our results provide molecular-level insight into the geometries and relative stabilities of the adsorption of phosphate and arsenate on magnetite surfaces, which is useful for interpretation of the mobility and bioavailability of these anions