Effective(kinetic freeze-out) temperature, transverse flow velocity, and kinetic freeze-out volume in high energy collisions

The transverse momentum spectra of different types of particles produced in central and peripheral gold–gold(Au–Au)and inelastic proton–proton(pp)collisions at the Relativistic Heavy Ion Collider,as well as in central and peripheral lead-lead(Pb–Pb)and pp collisions at the Large Hadron Collider,are analyzed by the multi-component standard(Boltzmann–Gibbs,Fermi–Dirac,and Bose–Einstein)distributions.The obtained results from the standard distribution give an approximate agreement with the measured experimental data by the STAR,PHENIX,and ALICE Collaborations.The behavior of the effective(kinetic freeze-out)temperature,transverse flow velocity,and kinetic freeze-out volume for particles with different masses is obtained,which observes the early kinetic freezeout of heavier particles as compared to the lighter particles.The parameters of emissions of different particles are observed to be different,which reveals a direct signature of the mass-dependent differential kinetic freeze-out.It is also observed that the peripheral nucleus–nucleus(AA)and pp collisions at the same center-of-mass energy per nucleon pair are in good agreement in terms of the extracted parameters.

K^+ Adsorption Kinetics of Fluvo-Aquic and Cinnamon Soil Under Different Temperature

The K+ adsorption kinetics of fluvo-aquic soil and cinnamon soil under different temperatureswere studied. The results showed: 1) The first order equations were the most suitable forfitting the adsorption under various temperature levels with constant K+ concentration indisplacing fluid. With temperature increasing, the fitness of Elovich equation increased,while those of power equation and parabolic diffusion equation decreased; 2)the apparentadsorption rate constant ka and the product of ka multiplied by the apparent equilibriumadsorption qincreased when temperature increased, while the apparent equilibrium adsorptionqreduced; 3)temperature influenced hardly the reaction order, the order of concentrationand adsorpton site were always 1 under various temperatures, if they were taken intoaccount simultaneously, the adsorption should be a two-order reaction process; 4)theGibbs free energy change △G of potassium adsorption were negative, ranged from -4444.56to -2450.63Jmol-1,and increased with temperature increasing, while enthalpy change △H,entropy change △S, apparent adsorption activation Ea, adsorption activation energy E1and desorption activation energy E2 were temperature-independent; 5)the adsorption wasspontaneous process with heat releasing and entropy dropping, fluvo-aquic soil releasedmore heat than cinnamon soil.

Ambiently fostering solid electrolyte interphase for low-temperature lithium metal batteries

Despite being a leading candidate to meet stringent energy targets,lithium(Li) metal batteries(LMBs)face severe challenges at low temperatures such as dramatic increase in impedance,capacity loss and dendrite growth.Unambiguously fingerprinting rate-limited factors of low-temperature LMBs would encourage targeted approaches to promote performances.Herein,the charge transfer impedance across solid electrolyte interphase(SEI) is identified to restrict battery operation under low temperature,and we propose a facile approach on the basis of ambiently fostering SEI(af-SEI) to facilitate charge transfer.The concept of af-SEI stems from kinetic benefits and structural merits to construct SEI at ambient temperature over low temperature developed SEI that is temporally consuming to achieve steady state and that is structurally defective to incur dendrite growth.The af-SEI allows ionically conductive and morphologically uniform layer on the anode surface,which exhibits a lower resistance and induces an even deposition of Li in the subsequent low temperature battery operation.Armed with af-SEI,the LMBs deliver the improved rate performance and prolonged cycle life when subjected to low temperature cycling.This work unveils the underlying causes that limit low temperature LMB performances,and enlightens the facile test protocols to build up favorable SEI,beyond scope of material and morphology design.

Degradation kinetics of larotaxel and identification of its degradation products in alkaline condition

Larotaxel, a new taxane compound prepared by partial synthesis from 10-deacetyl baccatin III, is active against tumors. In this research, a selective LC–MS method was developed and validated for the study of degradation kinetics of larotaxel, which was carried out in aqueous solutions with different pH（1.5, 3.0, 5.0, 6.5, 7.4, 9.0, 10 and 11.0） and temperature（0, 25, 37 and 45 °C）. The linear range was 0.5–25 μg/mL, the intra-and inter-day precisions were less than 7.0%, and accuracy ranged from 97.4–104.5% for each analyte. The observed rate obtained by measuring the remaining intact larotaxel was shown to follow first-order kinetics. The activation energies for degradation were 126.7 and 87.01 k J/mol at pH 1.5 and 11, respectively. Although larotaxel was stable in pH 5, 6.5 and 7.4 buffers at 37 °C for 24 h during our study, increasing or decreasing the pH of the solutions would decrease its stabilities. Moreover, three main degradation products in alkaline condition were separated by HPLC and identified by Q–TOF–MS. The three degradation products were confirmed as 10-deacetyl larotaxel, 7, 8-cyclopropyl baccatin Ⅲ and 10-deacetyl-7, 8-cyclopropyl baccatin Ⅲ.

Effect of temperature on anoxic metabolism of nitrites to nitrous oxide by polyphosphate accumulating organisms

Temperature is an important physical factor, which strongly influences biomass and metabolic activity. In this study, the effects of temperature on the anoxic metabolism of nitrite （NO2） to nitrous oxide （N2O） by polyphosphate accumulating organisms, and the process of the accumulation of N2O （during nitrite reduction）, which acts as an electron acceptor, were investigated using 91% ：e 4% Candidatus Accumulibacterphosphatis sludge. The results showed that N2O is accumulated when Accumulibacter first utilize nitrite instead of oxygen as the sole electron acceptor during the denitrifying phosphorus removal process. Properties such as nitrite reduction rate, phosphorus uptake rate, N2O reduction rate, and polyhydroxyalkanoate degradation rate were all influenced by temperature variation （over the range from 10 to 30℃ reaching maximum values at 25℃）. The reduction rate of N2O by N2O reductase was more sensitive to temperature when N2O was utilized as the sole electron acceptor instead of NO2, and the N2O reduction rates, ranging from 0.48 to 3.53 N2O-N/（hr.g VSS）, increased to 1.45 to 8.60 mg N2O-N/（hr·g VSS）. The kinetics processes for temperature variation of 10 to 30℃ were （01 = 1.140-1.216 and θ2 = 1.139-1.167）. In the range of 10℃ to 30℃, almost all of the anoxic stoichiometry was sensitive to temperature changes. In addition, a rise in N2O reduction activity leading to a decrease in N2O accumulation in long term operations at the optimal temperature （27℃ calculated by the Arrhenius model）.

Signatures of shear thinning-thickening transition in steady shear flows of dense non-Brownian yield stress systems

Steady shear flows of dense athermal systems composed of soft disks are investigated via non-equilibrium molecular dynamics simulations, from which we sort out links among the structure, dynamics, and shear rheology. The systems at rest are jammed packings of frictionless disks with a nonzero yield stress. Driven by low shear rates, the flows shear thin due to the presence of the nonzero yield stress, but transit to shear thickening above a crossover shear rate γc - At γc, we observe the strongest struc- tural anisotropy in the pair distribution function, which serves as the structural signature of the shear thinning-thickening tran- sition. We also observe dynamical signatures associated with the transition： At γc , scaling behaviors of both the mean squared displacement and relaxation time undergo apparent changes. By performing a simple energy analysis, we reveal an underlying condition for the shear thickening to occur： d（lnTg）/d（Inγ） 〉 2 with Tg the kinetic temperature. This condition is confirmed by simulations.