169 research outputs found
Sorption of CO2, CH4 and Their Mixtures in Amorphous Poly(2,6-dimethyl-1,4-phenylene)oxide (PPO)
Sorption of pure CO2 and CH4 and CO2/CH4 binary gas mixtures in amorphous glassy Poly(2,6-dimethyl-1,4-phenylene) oxide (PPO) at 35 °C up to 1000 Torr was investigated. Sorption experiments were carried out using an approach that combines barometry with FTIR spectroscopy in the transmission mode to quantify the sorption of pure and mixed gases in polymers. The pressure range was chosen to prevent any variation of the glassy polymer density. The solubility within the polymer of the CO2 present in the gaseous binary mixtures was practically coincident with the solubility of pure gaseous CO2, up to a total pressure of the gaseous mixtures equal to 1000 Torr and for CO2 mole fractions of ~0.5 mol mol-1 and ~0.3 mol mol-1. The Non-Equilibrium Thermodynamics for Glassy Polymers (NET-GP) modelling approach has been applied to the Non-Random Hydrogen Bonding (NRHB) lattice fluid model to fit the solubility data of pure gases. We have assumed here that no specific interactions were occurring between the matrix and the absorbed gas. The same thermodynamic approach has been then used to predict the solubility of CO2/CH4 mixed gases in PPO, resulting in a deviation lower than 9.5% from the experimental results for CO2 solubility
A Hyphenated Approach Combining Pressure-Decay and in Situ FT-NIR Spectroscopy to Monitor Penetrant Sorption and Concurrent Swelling in Polymers
A new hyphenated technique based on simultaneous in situ FT-NIR spectroscopy and pressure-decay measurements has been implemented to study sorption of low-molecular-weight compounds in polymeric membranes and the induced swelling of the matrix. The FT-NIR measurements are performed in the transmission mode and, besides sorption equilibrium and kinetics, allow also the straightforward measurement of polymer swelling. The pressure decay method is used to provide quantitative information on the concentration of penetrant sorbed in the polymer. This measurement, once combined with the photometric data, allows an accurate estimation of the molar absorptivity of the analytical peaks as well. To validate the new experimental approach, sorption of CO2 in polydimethylsiloxane at 35 °C and at pressures up to 9 bar has been investigated and the results are compared with available literature data
Survey on Adsorption of Low Molecular Weight Compounds in Cu-BTC MetalâOrganic Framework: Experimental Results and Thermodynamic Modeling
This contribution aims at providing a critical overview of experimental results for the sorption of low molecular weight compounds in the Cu-BTC MetalâOrganic Framework (MOF) and of their interpretation using available and new, specifically developed, theoretical approaches. First, a literature review of experimental results for the sorption of gases and vapors is presented, with particular focus on the results obtained from vibrational spectroscopy techniques. Then, an overview of theoretical models available in the literature is presented starting from semiempirical theoretical approaches suitable to interpret the adsorption thermodynamics of gases and vapors in Cu-BTC. A more detailed description is provided of a recently proposed Lattice Fluid approach, the Rigid Adsorbent Lattice Fluid (RALF) model. In addition, to deal with the cases where specific self- and cross-interactions (e.g., H-bonding, Lewis acid/Lewis base interactions) play a role, a modification of the RALF model, i.e., the RALFHB model, is introduced here for the first time. An extension of both RALF and RALFHB is also presented to cope with the cases in which the heterogeneity of the rigid adsorbent displaying a different kind of adsorbent cages is of relevance, as it occurs for the adsorption of some low molecular weight substances in Cu-BTC MOF
Chemical Vapour Deposition GrapheneâPMMA Nanolaminates for Flexible Gas Barrier
Successful ways of fully exploiting the excellent structural and multifunctional performance of graphene and related materials are of great scientific and technological interest. New opportunities are provided by the fabrication of a novel class of nanocomposites with a nanolaminate architecture. In this work, by using the iterative lift-off/float-on process combined with wet depositions, we incorporated cm-size graphene monolayers produced via Chemical Vapour Deposition into a poly (methyl methacrylate) (PMMA) matrix with a controlled, alternate-layered structure. The produced nanolaminate shows a significant improvement in mechanical properties, with enhanced stiffness, strength and toughness, with the addition of only 0.06 vol% of graphene. Furthermore, oxygen and carbon dioxide permeability measurements performed at different relative humidity levels, reveal that the addition of graphene leads to significant reduction of permeability, compared to neat PMMA. Overall, we demonstrate that the produced grapheneâPMMA nanolaminate surpasses, in terms of gas barrier properties, the traditional discontinuous grapheneâparticle composites with a similar filler content. Moreover, we found that the gas permeability through the nanocomposites departs from a monotonic decrease as a function of relative humidity, which is instead evident in the case of the pure PMMA nanolaminate. This work suggests the possible use of Chemical Vapour Deposition grapheneâpolymer nanolaminates as a flexible gas barrier, thus enlarging the spectrum of applications for this novel material
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Surface chemistry of alanine on Ni{111}
The adsorption of L-alanine on Ni{111} has been studied as a 10 model of enantioselective heterogeneous catalysts. Synchrotron-based X-ray 11 photoelectron spectroscopy and near-edge X-ray absorption fine structure 12 (NEXAFS) spectroscopy were used to determine the chemical state, bond 13 coordination, and out-of-plane orientation of the molecule on the surface.
14 Alanine adsorbs in anionic and zwitterionic forms between 250 and â320 K. 15 NEXAFS spectra exhibit a strong angular dependence of the Ï* resonance
16 associated with the carboxylate group, which is compatible with two distinct 17 orientations with respect to the surface corresponding to the bidentate and
18 tridentate binding modes. Desorption and decomposition begin together at 19 â300 K, with decomposition occurring in a multistep process up to â450 K. Comparison with previous studies of amino acid 20 adsorption on metal surfaces shows that this is among the lowest decomposition temperatures found so far and lower than typical 21 temperatures used for hydrogenation reactions where modified Ni catalysts are used
The analytical method algorithm for trigger primitives generation at the LHC drift tubes detector
The Compact Muon Solenoid (CMS) experiment prepares its Phase-2 upgrade for the high-luminosity era of the
LHC operation (HL-LHC). Due to the increase of occupancy, trigger latency and rates, the full electronics of the CMS Drift Tube (DT) chambers will need to be replaced. In the new design, the time bin for the digitization of the chamber signals will be of around 1 ns, and the totality of the signals will be forwarded asynchronously
to the service cavern at full resolution. The new backend system will be in charge of building the trigger
primitives of each chamber. These trigger primitives contain the information at chamber level about the muon
candidates position, direction, and collision time, and are used as input in the L1 CMS trigger. The added
functionalities will improve the robustness of the system against ageing. An algorithm based on analytical
solutions for reconstructing the DT trigger primitives, called Analytical Method, has been implemented both
as a software C++ emulator and in firmware. Its performance has been estimated using the software emulator
with simulated and real data samples, and through hardware implementation tests. Measured efficiencies are
96 to 98% for all qualities and time and spatial resolutions are close to the ultimate performance of the
DT chambers. A prototype chain of the HL-LHC electronics using the Analytical Method for trigger primitive
generation has been installed during Long Shutdown 2 of the LHC and operated in CMS cosmic data taking
campaigns in 2020 and 2021. Results from this validation step, the so-called Slice Test, are presented
SND@LHC: The Scattering and Neutrino Detector at the LHC
SND@LHC is a compact and stand-alone experiment designed to perform measurements with neutrinos produced at the LHC in the pseudo-rapidity region of . The experiment is located 480 m downstream of the ATLAS interaction point, in the TI18 tunnel. The detector is composed of a hybrid system based on an 830 kg target made of tungsten plates, interleaved with emulsion and electronic trackers, also acting as an electromagnetic calorimeter, and followed by a hadronic calorimeter and a muon identification system. The detector is able to distinguish interactions of all three neutrino flavours, which allows probing the physics of heavy flavour production at the LHC in the very forward region. This region is of particular interest for future circular colliders and for very high energy astrophysical neutrino experiments. The detector is also able to search for the scattering of Feebly Interacting Particles. In its first phase, the detector will operate throughout LHC Run 3 and collect a total of 250
ATHENA detector proposal - a totally hermetic electron nucleus apparatus proposed for IP6 at the Electron-Ion Collider
ATHENA has been designed as a general purpose detector capable of delivering the full scientific scope of the Electron-Ion Collider. Careful technology choices provide fine tracking and momentum resolution, high performance electromagnetic and hadronic calorimetry, hadron identification over a wide kinematic range, and near-complete hermeticity.This article describes the detector design and its expected performance in the most relevant physics channels. It includes an evaluation of detector technology choices, the technical challenges to realizing the detector and the R&D required to meet those challenges
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