625 research outputs found

    Permeation of water as a tool for characterizing the effect of solvent, film thickness and water solubility in cellulose acetate membranes

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    Cellulose acetate membranes have been used in many applications; of particular interest are reverse osmosis systems, and as a neutral matrix for incorporation of different polymers (e.g., conducting polymers), inorganic ions (e.g., lanthanides) and organic (e.g., pharmaceutical) compounds. The properties of the new polymers derived from cellulose acetate or blends depend on those of cellulose acetate. This work presents an attempt to find links between thermodynamic and kinetic properties of cellulose acetate membranes in equilibrium with water. Water diffusion coefficients in cellulose acetate membranes are reported, measured with a simple water permeation technique. The comparison of these values with the percentage of water uptake and polymer thickness leads to interesting conclusions related with different polymer properties.http://www.sciencedirect.com/science/article/B6TWW-4DVBFCN-7/1/63e48f8aac1513c35feeaa6c746621e

    Production of He-4 and (4) in Pb-Pb collisions at root(NN)-N-S=2.76 TeV at the LHC

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    Results on the production of He-4 and (4) nuclei in Pb-Pb collisions at root(NN)-N-S = 2.76 TeV in the rapidity range vertical bar y vertical bar <1, using the ALICE detector, are presented in this paper. The rapidity densities corresponding to 0-10% central events are found to be dN/dy4(He) = (0.8 +/- 0.4 (stat) +/- 0.3 (syst)) x 10(-6) and dN/dy4 = (1.1 +/- 0.4 (stat) +/- 0.2 (syst)) x 10(-6), respectively. This is in agreement with the statistical thermal model expectation assuming the same chemical freeze-out temperature (T-chem = 156 MeV) as for light hadrons. The measured ratio of (4)/He-4 is 1.4 +/- 0.8 (stat) +/- 0.5 (syst). (C) 2018 Published by Elsevier B.V.Peer reviewe

    Transport of non-associated electrolytes in acrylamide hydrogels

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    Diffusion of non-associated electrolytes (LiCl and KCl) in different hydrogels has been studied to identify the mechanism of electrolyte interaction with the structure of hydrogels and its dependence on electrolyte concentration and thermodynamic features of the electrolyte. Hydrogel membranes have been prepared from acrylamide (AAm) using N,N′-methylene-bis-acrylamide (MBAAm) as the cross-linker. Properties of membranes have been altered varying the content of cross-linker. Integral diffusion coefficients of potassium chloride and lithium chloride in the hydrogel membranes have been compared with mutual diffusion coefficients of those electrolytes in aqueous solutions. The study of electrolyte diffusion was supported by data on water solubility in hydrogels (degree of swelling, and sorption and desorption isotherms) showing dependence of electrolyte diffusion coefficient on water content inside polymer matrix. Thermodynamic study showed irreversible character of the sorption of solutes, probably due to acidic hydrolysis of amide groups of gels. The main features, which characterise properties of aqueous solution of strong electrolytes, remain in polymer matrix thus defining diffusion coefficients and other parameters representative of electrolyte transport in polyacrylamide hydrogels. © 2001 Elsevier Science B.V. All rights reserved.SCOPUS: ar.jinfo:eu-repo/semantics/publishe

    Permeation of water as a tool for characterizing the effect of solvent, film thickness and water solubility in cellulose acetate membranes

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    Cellulose acetate membranes have been used in many applications; of particular interest are reverse osmosis systems, and as a neutral matrix for incorporation of different polymers (e.g., conducting polymers), inorganic ions (e.g., lanthanides) and organic (e.g., pharmaceutical) compounds. The properties of the new polymers derived from cellulose acetate or blends depend on those of cellulose acetate. This work presents an attempt to find links between thermodynamic and kinetic properties of cellulose acetate membranes in equilibrium with water. Water diffusion coefficients in cellulose acetate membranes are reported, measured with a simple water permeation technique. The comparison of these values with the percentage of water uptake and polymer thickness leads to interesting conclusions related with different polymer properties.http://www.sciencedirect.com/science/article/B6TWW-4DVBFCN-7/1/63e48f8aac1513c35feeaa6c746621e

    Combined sorption/transport of sodium dodecyl sulfate and hydrochloric acid in a blend of cellulose acetate butyrate with cellulose acetate hydrogen phthalate

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    The transport of hydrochloric acid (0.001-0.1 M) and sodium dodecyl sulfate (0.001-0.1 M) has been measured through a membrane consisting of a blend of cellulose acetate butyrate and cellulose acetate hydrogen phthalate. The cellulose derivative blend is suggested to suffer an alteration in the degree of hydrophobicity when in equilibrium with sodium dodecyl sulfate (SDS) through hemimicelle formation. An increase in surface hydrophobicity of the blend when in equilibrium with SDS solution was observed by fluorescence measurements using the vibronic bands of the probe pyrene, as well as by water desorption kinetics; a decrease of the effective diffusion coefficients from 1.2 × 10-11 m2 s-1 in the absence of SDS to approximately 2 × 10-13 m2 s-1 in its presence was found. The value obtained for the mutual diffusion coefficient of HCl in the concentration range 0.001-0.1 M (D=4.2×10-14 m2 s-1) shows also that the membrane presents hydrophobic features. The flux of SDS in the blend membrane at different pH values shows two distinct permeation rates depending on the cmc. However, from the calculation of permeability coefficients at SDS concentrations below the cmc a clear decrease in P is found, whilst, at concentrations above the cmc the permeability coefficients are nearly constant, only showing a slightly increase. The diffusion coefficients of SDS in the blend increase over the whole SDS concentration range analysed and show an effective diffusion coefficient 2-3 orders of magnitude below the diffusion coefficients of SDS in aqueous solutions. This fact suggests that the only diffusing species are SDS unimers. The presence of HCl in the SDS bulk solution has the effect of increasing the permeability and diffusion coefficients. Mutual analysis of permeation and diffusion coefficients and sorption isotherms shows that, on decreasing the pH, the interactions between SDS and the polymer network decrease. This is also reflected in a clear decrease of the hydrophobic interactions between the diffusing and polymeric species, provoked by a decrease in the unimer-unimer association.http://www.sciencedirect.com/science/article/B6TWW-49WPFVC-K/1/a590044f98d090805ffa5445fba983a

    Multiplicity dependence of light (anti-)nuclei production in p–Pb collisions at sNN=5.02 TeV

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    The measurement of the deuteron and anti-deuteron production in the rapidity range −1 < y < 0 as a function of transverse momentum and event multiplicity in p–Pb collisions at √sNN = 5.02 TeV is presented. (Anti-)deuterons are identified via their specific energy loss dE/dx and via their time-of- flight. Their production in p–Pb collisions is compared to pp and Pb–Pb collisions and is discussed within the context of thermal and coalescence models. The ratio of integrated yields of deuterons to protons (d/p) shows a significant increase as a function of the charged-particle multiplicity of the event starting from values similar to those observed in pp collisions at low multiplicities and approaching those observed in Pb–Pb collisions at high multiplicities. The mean transverse particle momenta are extracted from the deuteron spectra and the values are similar to those obtained for p and particles. Thus, deuteron spectra do not follow mass ordering. This behaviour is in contrast to the trend observed for non-composite particles in p–Pb collisions. In addition, the production of the rare 3He and 3He nuclei has been studied. The spectrum corresponding to all non-single diffractive p-Pb collisions is obtained in the rapidity window −1 < y < 0 and the pT-integrated yield dN/dy is extracted. It is found that the yields of protons, deuterons, and 3He, normalised by the spin degeneracy factor, follow an exponential decrease with mass number

    Measurement of inclusive J/ψ\psi pair production cross section in pp collisions at s=13\sqrt{s} = 13 TeV

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    International audienceThe production cross section of inclusive J/ψ\psi pairs in pp collisions at a centre-of-mass energy s=13\sqrt{s} = 13 TeV is measured with ALICE. The measurement is performed for J/ψ\psi in the rapidity interval 2.502.5 0. The production cross section of inclusive J/ψ\psi pairs is reported to be 10.3±2.3(stat.)±1.3(syst.)10.3 \pm 2.3 {\rm (stat.)} \pm 1.3 {\rm (syst.)} nb in this kinematic interval. The contribution from non-prompt J/ψ\psi (i.e. originated from beauty-hadron decays) to the inclusive sample is evaluated. The results are discussed and compared with data

    Inclusive and multiplicity dependent production of electrons from heavy-flavour hadron decays in pp and p-Pb collisions

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    International audienceMeasurements of the production of electrons from heavy-flavour hadron decays in pp collisions at s=13\sqrt{s} = 13 TeV at midrapidity with the ALICE detector are presented down to a transverse momentum (pTp_{\rm T}) of 0.2 GeV/c/c and up to pT=35p_{\rm T} = 35 GeV/c/c, which is the largest momentum range probed for inclusive electron measurements in ALICE. In p-Pb collisions, the production cross section and the nuclear modification factor of electrons from heavy-flavour hadron decays are measured in the pTp_{\rm T} range 0.5<pT<260.5 < p_{\rm T} < 26 GeV/c/c at sNN=8.16\sqrt{s_{\rm NN}} = 8.16 TeV. The nuclear modification factor is found to be consistent with unity within the statistical and systematic uncertainties. In both collision systems, first measurements of the yields of electrons from heavy-flavour hadron decays in different multiplicity intervals normalised to the multiplicity-integrated yield (self-normalised yield) at midrapidity are reported as a function of the self-normalised charged-particle multiplicity estimated at midrapidity. The self-normalised yields in pp and p-Pb collisions grow faster than linear with the self-normalised multiplicity. A strong pTp_{\rm T} dependence is observed in pp collisions, where the yield of high-pTp_{\rm T} electrons increases faster as a function of multiplicity than the one of low-pTp_{\rm T} electrons. The measurement in p-Pb collisions shows no pTp_{\rm T} dependence within uncertainties. The self-normalised yields in pp and p-Pb collisions are compared with measurements of other heavy-flavour, light-flavour, and strange particles, and with Monte Carlo simulations

    Observation of medium-induced yield enhancement and acoplanarity broadening of low-pTp_\mathrm{T} jets from measurements in pp and central Pb-Pb collisions at sNN=5.02\sqrt{s_{\rm NN}}=5.02 TeV

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    International audienceThe ALICE Collaboration reports the measurement of semi-inclusive distributions of charged-particle jets recoiling from a high transverse momentum (high pTp_{\rm T}) hadron trigger in proton-proton and central Pb-Pb collisions at sNN=5.02\sqrt{s_{\rm NN}} = 5.02 TeV. A data-driven statistical method is used to mitigate the large uncorrelated background in central Pb-Pb collisions. Recoil jet distributions are reported for jet resolution parameter R=0.2R=0.2, 0.4, and 0.5 in the range 7<pT,jet<1407 < p_{\rm T,jet} < 140 GeV/c/c and trigger-recoil jet azimuthal separation π/2<Δφ<π\pi/2 < \Delta\varphi < \pi. The measurements exhibit a marked medium-induced jet yield enhancement at low pTp_{\rm T} and at large azimuthal deviation from Δφπ\Delta\varphi\sim\pi. The enhancement is characterized by its dependence on Δφ\Delta\varphi, which has a slope that differs from zero by 4.7σ\sigma. Comparisons to model calculations incorporating different formulations of jet quenching are reported. These comparisons indicate that the observed yield enhancement arises from the response of the QGP medium to jet propagation

    Probing the Chiral Magnetic Wave with charge-dependent flow measurements in Pb-Pb collisions at the LHC

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    International audienceThe Chiral Magnetic Wave (CMW) phenomenon is essential to provide insights into the strong interaction in QCD, the properties of the quark-gluon plasma, and the topological characteristics of the early universe, offering a deeper understanding of fundamental physics in high-energy collisions. Measurements of the charge-dependent anisotropic flow coefficients are studied in Pb-Pb collisions at center-of-mass energy per nucleon-nucleon collision sNN=\sqrt{s_{\mathrm{NN}}}= 5.02 TeV to probe the CMW. In particular, the slope of the normalized difference in elliptic (v2v_{2}) and triangular (v3v_{3}) flow coefficients of positively and negatively charged particles as a function of their event-wise normalized number difference, is reported for inclusive and identified particles. The slope r3Normr_{3}^{\rm Norm} is found to be larger than zero and to have a magnitude similar to r2Normr_{2}^{\rm Norm}, thus pointing to a large background contribution for these measurements. Furthermore, r2Normr_{2}^{\rm Norm} can be described by a blast wave model calculation that incorporates local charge conservation. In addition, using the event shape engineering technique yields a fraction of CMW (fCMWf_{\rm CMW}) contribution to this measurement which is compatible with zero. This measurement provides the very first upper limit for fCMWf_{\rm CMW}, and in the 10-60% centrality interval it is found to be 26% (38%) at 95% (99.7%) confidence level
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