Charged-particle multiplicity density at midrapidity in central Pb-Pb collisions at sqrt[S(NN)] = 2.76 TeV

The first measurement of the charged-particle multiplicity density at midrapidity in Pb-Pb collisions at a center-of-mass energy per nucleon pair √ S NN = 2.76 TeV is presented. For an event sample corresponding to the most central 5% of the hadronic cross section, the pseudorapidity density of primary charged particles at midrapidity is 1584 ± 4(stat) ± 76(syst), which corresponds to 8.3 ± 0.4(syst) per participating nucleon pair. This represents an increase of about a factor 1.9 relative to pp collisions at similar collision energies, and about a factor 2.2 to central Au-Au collisions at √ S NN = 2.76 TeV. This measurement provides the first experimental constraint for models of nucleus-nucleus collisions at LHC energies.     

Elliptic flow of charged particles in Pb-Pb collisions at sqrt[S(NN)] = 2.76 TeV

We report the first measurement of charged particle elliptic flow in Pb-Pb collisions at sqrt[S(NN)] =2.76 TeV with the ALICE detector at the CERN Large Hadron Collider. The measurement is performed in the central pseudorapidity region (|η|<0.8) and transverse momentum range 0.2

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An ESR Approach to the Estimation of the Rate Constants of the Addition and Fragmentation Processes Involved in the RAFT Polymerization of Styrene

The reversible‐addition‐fragmentation chain transfer (RAFT) controlled radical polymerization of such vinylic monomers as styrene (= ethenylbenzene) has gained increasing popularity in current years. While there is a general agreement on the mechanism of RAFT polymerization, there is an ongoing debate about the values of the rate constants of its key steps, i.e., the addition of the propagating radicals to the mediator and the fragmentation of the resulting spin adducts. By carrying out an ESR spectroscopic investigation of the AIBN‐initiated polymerization of styrene (AIBN = 2,2′‐azobis[2‐methylpropanenitrile]), mediated by benzyl (diethoxyphosphoryl)dithioformate ( 5 ) as RAFT agent, we were able to detect and characterize four different radical species involved in the process. By reproducing their concentration–time profiles through a kinetic model, the addition and fragmentation rate constants at 90° of the propagating radicals to and from the mediator were estimated to be ca.10⁷ M ^?1 s^?1 and ca. 10³ s^?1, respectively. The validity of the kinetic model was supported by hybrid meta DFT calculations with the BB1K functional that predicted addition‐ and fragmentation‐rate‐constant values in good agreement with those estimated from the ESR experiments.     

Measurement of weak transmittances by stochastic resonance

We use stochastic resonance to measure weak transmittance amplitudes that are below the instrumental detection limit. Gaussian noise is added to the subthreshold (chopped) transmittance signal T(t) before detection by a crossing detector that uses a dc reference signal B>0. Without noise, no measurement is possible because T(t)相似文献   

J/ψ polarization in pp collisions at √s=7 TeV

The ALICE Collaboration has studied J/ψ production in pp collisions at √s=7 TeV at the LHC through its muon pair decay. The polar and azimuthal angle distributions of the decay muons were measured, and results on the J/ψ polarization parameters λ(θ) and λ(φ) were obtained. The study was performed in the kinematic region 2.5相似文献   

Imaging of EdU, an alkyne-tagged cell proliferation probe, by Raman microscopy

Click-free imaging of the nuclear localization of an alkyne-tagged cell proliferation probe, EdU, in living cells was achieved for the first time by means of Raman microscopy. The alkyne tag shows an intense Raman band in a cellular Raman-silent region that is free of interference from endogenous molecules. This approach may eliminate the need for click reactions in the detection of alkyne-labeled molecules.     

Higher harmonic anisotropic flow measurements of charged particles in Pb-Pb collisions at sqrt(s(NN)) = 2.76 TeV

We report on the first measurement of the triangular v3, quadrangular v4, and pentagonal v5 charged particle flow in Pb-Pb collisions at sqrt(s(NN)) = 2.76 TeV measured with the ALICE detector at the CERN Large Hadron Collider. We show that the triangular flow can be described in terms of the initial spatial anisotropy and its fluctuations, which provides strong constraints on its origin. In the most central events, where the elliptic flow v2 and v3 have similar magnitude, a double peaked structure in the two-particle azimuthal correlations is observed, which is often interpreted as a Mach cone response to fast partons. We show that this structure can be naturally explained from the measured anisotropic flow Fourier coefficients.     

Centrality dependence of the charged-particle multiplicity density at midrapidity in Pb-Pb collisions at sqrt[s(NN)] = 2.76 TeV

The centrality dependence of the charged-particle multiplicity density at midrapidity in Pb-Pb collisions at sqrt[s_{NN}]=2.76 TeV is presented. The charged-particle density normalized per participating nucleon pair increases by about a factor of 2 from peripheral (70%-80%) to central (0%-5%) collisions. The centrality dependence is found to be similar to that observed at lower collision energies. The data are compared with models based on different mechanisms for particle production in nuclear collisions.     

Halide‐ion‐assisted increase of surface‐enhanced hyper‐Raman scattering: a clear observation of the chemical effect

We show that the increase of surface‐enhanced hyper‐Raman scattering (SEHRS) intensity of organic dye molecules adsorbed on single silver (Ag) colloid aggregate in the presence of halide ions is a direct evidence of the chemical effect in the enhancement mechanism. Time‐dependent SEHRS measurements before and after adding halide ions enabled us to distinctly observe the chemical effect. The presence of the halide ions results to a more stable chemical interaction between metal and dye molecule, making it more resistant against photodegradation effects. This study can contribute in elucidating the chemical effect mechanism and aid in the development of SEHRS as a useful spectroscopic tool. Copyright © 2008 John Wiley & Sons, Ltd.