Study on the assimilation of the sulphate reaction rates based on WRF-Chem/DART

Sulphate(SO_(4)^(2-))is a main component of PM_(2.5)in China.The chemical formation mechanisms of sulphate are complex,and many air quality models have been used to analyse these mechanisms.To improve the accuracy of Weather Research Forecast-Chemistry(WRF-Chem)on sulphate,an alternative method is proposed in this paper.Moreover,data assimilation is performed to adjust the chemical reaction rates of sulphate.Based on the original reactions,a new sulphate parameterisation scheme,which includes two hypothetical reactions and six undetermined parameters,was added.Based on the WRF-Chem/DART(Data Assistance Research Testbed)system,the near-ground concentrations of SO_(4)^(2-),SO_(2),NO_(2),O_(3)and particulate matter are assimilated to adjust the six parameters.After adjusting the parameters,the new scheme can effectively solve the underestimation of SO_(4)^(2-)and overestimation of SO_(2).The simulation of SO_(4)^(2-)improved as the mean bias changed from-13.1μg m^(-3)to 3.5μg m^(-3)while SO_(2)improved from 17.0μg m^(-3)to 6.3μg m^(-3).The temporal and spatial variation characteristics predicted by the new scheme are consistent with the theoretical research results,indicating that the complex mechanism of sulphate formation could be replaced by the temporal and spatial variation characteristics predicted by the new scheme and that the parameters can be adjusted by data assimilation.Furthermore,the reaction rates of the SO_(4)^(2-)parameterisation scheme of the WRF-Chem model are improved in this study,and a new method for improving the accuracy of the air quality model is provided.

Approaching Ultimate Synthesis Reaction Rate of Ni-Rich Layered Cathodes for Lithium-Ion Batteries

Nickel-rich layered oxide LiNi_(x)Co_(y)MnzO_(2)(NCM,x+y+z=1)is the most promising cathode material for high-energy lithium-ion batteries.However,conventional synthesis methods are limited by the slow heating rate,sluggish reaction dynamics,high energy consumption,and long reaction time.To overcome these chal-lenges,we first employed a high-temperature shock(HTS)strategy for fast synthesis of the NCM,and the approaching ultimate reaction rate of solid phase transition is deeply investigated for the first time.In the HTS process,ultrafast average reaction rate of phase transition from Ni_(0.6)Co_(0.2)Mn_(0.2)(OH)_(2) to Li-containing oxides is 66.7(%s^(-1)),that is,taking only 1.5 s.An ultrahigh heating rate leads to fast reaction kinetics,which induces the rapid phase transition of NCM cathodes.The HTS-synthesized nickel-rich layered oxides perform good cycling performances(94%for NCM523,94%for NCM622,and 80%for NCM811 after 200 cycles at 4.3 V).These findings might also assist to pave the way for preparing effectively Ni-rich layered oxides for lithium-ion batteries.

Ergodicity of Reversible Reaction Diffusion Processes with General Reaction Rates

In this paper,a class of reaction diffusion processes with general reaction rates is studied.A necessary and sufficient condition for the reversibility of this calss of reaction diffusion processes is given,and then the ergodicity of these processes is proved.

New Generation of Experiments for the Investigation of Stellar (p,γ) Reaction Rates Using SAMURAI

The future experimental campaign with the SAMURAI setup at RIKEN will explore a wide range of neutron-deficient nuclei with a particular focus on the most critical(p, γ) reaction rates relevant to the astrophysical rp-process in type-I X-ray bursts(XRB). Intense radioactive-ion(RI) beams at an energy of a few hundred Me V/nucleon will be deployed to populate proton-unbound states in the nuclei of interest through the Coulomb excitation or nucleon-removal processes. The decay of these states into a proton and a heavy residue will be measured using complete kinematics and the information about time reversal proton-capture process will be obtained. This method will provide the vital experimental data on the resonances, which dominate the stellar(p, γ) reaction rates, as well as on the direct proton-capture process for some other cases. The experimental setup will utilize for the first time the High-Resolution90?-mode of the SAMURAI spectrometer in combination with the existing detection systems, including custom-designed Si-strip detectors for simultaneous detection and tracking of heavy ions and protons emitted from the target. The details of the experimental method and the utilized apparatus are discussed in this paper.

Investigation of the ^(121)Sb(α,γ)^(125)I reaction cross-section calculations at astrophysical energies

Proton-rich nuclei are synthesized via photodisintegration and reverse reactions.To examine this mechanism and reproduce the observed p-nucleus abundances,it is crucial to know the reaction rates and thereby the reaction cross sections of many isotopes.Given that the number of experiments on the reactions in astrophysical energy regions is very rare,the reaction cross sections are determined by theoretical methods whose accuracy should be tested.In this study,given that ^(121)Sb is a stable seed isotope located in the region of medium-mass p-nuclei,we investigated the cross sections and reaction rates of the ^(121)Sb(α,γ)^(125)I reaction using the TALYS computer code with 432 different combinations of input parameters(OMP,LDM,and SFM).The optimal model combinations were determined using the threshold logic unit method.The theoretical reaction cross-sectional results were compared with the experimental results reported in the literature.The reaction rates were determined using the two input parameter sets most compatible with the measurements,and they were compared with the reaction rate databases:STARLIB and REACLIB.

A new Ignition-Growth reaction rate model for shock initiation

Accurately predicting reactive flow is a challenge when characterizing an explosive under external shock stimuli as the shock initiation time is on the order of a microsecond.The present study constructs a new Ignition-Growth reaction rate model,which can describe the shock initiation processes of explosives with different initial densities,particle sizes and loading pressures by only one set of model parameters.Compared with the Lee-Tarver reaction rate model,the new Ignition-Growth reaction rate model describes better the shock initiation process of explosives and requires fewer model parameters.Moreover,the shock initiation of a 2,4-Dinitroanisole(DNAN)-based melt-cast explosive RDA-2(DNAN/HMX(octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazoncine)/aluminum)are investigated both experimentally and numerically.A series of shock initiation experiments is performed with manganin piezoresistive pressure gauges and corresponding numerical simulations are carried out with the new Ignition-Growth reaction rate model.The RDA-2 explosive is found to have higher critical initiation pressure and lower shock sensitivity than traditional explosives(such as the Comp.B explosive).The calibrated reaction rate model parameters of RDA-2 could provide numerical basis for its further application.

Study of primordial deuterium abundance in Big Bang nucleosynthesis

Big Bang nucleosynthesis(BBN)theory predicts the primordial abundances of the light elements^(2) H(referred to as deuterium,or D for short),^(3)He,^(4)He,and^(7) Li produced in the early universe.Among these,deuterium,the first nuclide produced by BBN,is a key primordial material for subsequent reactions.To date,the uncertainty in predicted deuterium abundance(D/H)remains larger than the observational precision.In this study,the Monte Carlo simulation code PRIMAT was used to investigate the sensitivity of 11 important BBN reactions to deuterium abundance.We found that the reaction rate uncertainties of the four reactions d(d,n)^(3)He,d(d,p)t,d(p,γ)^(3)He,and p(n,γ)d had the largest influence on the calculated D/H uncertainty.Currently,the calculated D/H uncertainty cannot reach observational precision even with the recent LUNA precise d(p,γ)^(3) He rate.From the nuclear physics aspect,there is still room to largely reduce the reaction-rate uncertainties;hence,further measurements of the important reactions involved in BBN are still necessary.A photodisintegration experiment will be conducted at the Shanghai Laser Electron Gamma Source Facility to precisely study the deuterium production reaction of p(n,γ)d.

Kinetics and mechanism of titanium hydride powder and aluminum melt reaction

Based on the measurement of the released hydrogen gas pressure （PH2）, the reaction kinetics between TiH2 powder and pure aluminum melt was studied at various temperatures. After cooling the samples, the interface of TiH2 powder and aluminum melt was studied. The results show that the-time curves have three regions; in the first and second regions, the rate of reaction conforms zero and one order, respectively; in the third region, the hydrogen gas pressure remains constant and the rate of reaction reaches zero. The main factors that control the rate of reaction in the first and second regions are the penetration of hydrogen atoms in the titanium lattice and the chemical reaction between molten aluminum and titanium, respectively. According to the main factors that control the rate of reaction, three temperature ranges are considered for the reaction mechanism： （a） 700-750°C, （b） 750-800°C, and （c） 800-1000°C. In the first temperature range, the reaction is mostly under the control of chemical reaction; at the temperature range of 750 to 800°C, the reaction is controlled by the diffusion and chemical reaction; at the third temperature range （800-1000°C）, the dominant controlling mechanism is diffusion.

Energy diffusion controlled reaction rate in dissipative Hamiltonian systems

In this paper the energy diffusion controlled reaction rate in dissipative Hamiltonian systems is investigated by using the stochastic averaging method for quasi Hamiltonian systems. The boundary value problem of mean first- passage time （MFPT） of averaged system is formulated and the energy diffusion controlled reaction rate is obtained as the inverse of MFPT. The energy diffusion controlled reaction rate in the classical Kramers bistable potential and in a two-dimensional bistable potential with a heat bath are obtained by using the proposed approach respectively. The obtained results are then compared with those from Monte Carlo simulation of original systems and from the classical Kraraers theory. It is shown that the reaction rate obtained by using the proposed approach agrees well with that from Monte Carlo simulation and is more accurate than the classical Kramers rate.

Nitrogen-Doped Hierarchical Heterostructured Aerophobic MoS_(x)/Ni_(3)S_(2)Nanowires by One-pot Synthesis:System Engineering and Synergistic Effect in Electrocatalysis of Hydrogen Evolution Reaction

Non-noble metal electrocatalysis has witnessed rapid and profound performance improvements owing to the emergence of advanced nanosynthetic techniques.Integration of these nanotechniques can lead to synergistic performance enhancement,but such system-engineering strategies are difficult to achieve because of the lack of effective synthesis method.We hereby demonstrate an integrated approach that combines most of the existing nanotechniques in a facile one-pot synthesis.Material characterization reveals that the product shows key features intended by techniques including morphological,structural,doping,heterointerface,and surface wetting engineering.The as-obtained nitrogen-doped hierarchical heterostructured MoS_(x)/Ni_(3)S_(2)nanowires show an overpotential that is only50 mV higher than commercial Pt/C for hydrogen evolution reaction over current densities from 10 to 150 mA cm^(-2).Correlations between the adopted nanotechniques and the electrochemical reaction rates are established by evaluating the impacts of individual techniques on the activation energy,pre-exponential factor,and transfer coefficient.This indepth analysis provides a full account of the synergistic effects and the overall improvement in electrocatalytic performance of hydrogen evolution reaction.This work manifests a generic strategy for multipurpose material design in non-noble metal electrocatalysis.

Key Role of Some Specific Occupied Molecular Orbitals of Short Chain n-Alkanes in Their Surface Tension and Reaction Rate Constants with Hydroxyl Radicals: DFT Study

Basing on the DFT calculations we propose the new theoretical model which describes both the surface tension σ of the short chain n-alkanes at their normal boiling points and their reaction rate constants with hydroxyl radicals OH• (at 297 ± 2 K) on the basis of their molecular orbital electronic characteristics. It has been shown that intermolecular dispersion attraction within the surface liquid monolayer of these compounds, as well as their reaction rate constants k with OH• radicals are determined by the energies Eorb of the specific occupied molecular orbitals which are the same in the determination of both the above physico-chemical characteristics of the studied n-alkanes. The received regression equations confirm the theoretically found dependences between the quantities of σ and k and the module |Eorb|. For the compounds under study this fact indicates the key role of their electronic structure particularities in determination of both the physical (surface tension) and the chemical (reaction rate constants) properties.

Determination of the stellar reaction rate for ^(12)C(α, γ)^(16)O: using a new expression with the reaction mechanism

The astrophysical reaction rate of 12C（α,γ）16O plays a key role in massive star evolution. However, this reaction rate and its uncertainties have not been well determined yet, especially at T9=0.2. The existing results even disagree with each other to a certain extent. In this paper, the El, E2 and total （E1＋E2） 12C（α,γ）16O reaction rates are calculated in the temperature range from T9=0.3 to 2 according to all the available cross section data. A new analytic expression of the 12C（α,γ）16O reaction rate is brought forward based on the reaction mechanism. In this expression, each part embodies the underlying physics of the reaction. Unlike previous works, some physical parameters are chosen from experimental results directly, instead of all the parameters obtained from fitting. These parameters in the new expression, with their 3σ fit errors, are obtained from fit to our calculated reaction rate from T9=0.3 to 2. Using the fit results, the analytic expression of 12C（α,γ）16Oreaction rate is extrapolated down to T9=0.05 based on the underlying physics. The 12C（α,γ）16O reaction rate at T9=0.2 is （8.78 ± 1.52） × 10^15 cm3s^-1mol^-1. Some comparisons and discussions about our new 12C（α,γ）16Oreaction rate are presented, and the contributions of the reaction rate correspond to the different part of reaction mechanism are given. The agreements of the reaction rate below T9=2 between our results and previous works indicate that our results are reliable, and they could be included in the astrophysical reaction rate network. Furthermore, we believe our method to investigate the 12C（α,γ）16O reaction rate is reasonable, and this method can also be employed to study the reaction rate of other astrophysical reactions. Finally, a new constraint of the supernovae production factor of some isotopes are illustrated according to our 12C（α,γ）16O reaction rates.

A melt-cast Duan-Zhang-Kim mesoscopic reaction rate model and experiment for shock initiation of melt-cast explosives

A melt-cast Duan-Zhang-Kim(DZK)mesoscopic reaction rate model is developed for the shock initiation of melt-cast explosives based on the pore collapse hot-spot ignition mechanism.A series of shock initiation experiments was performed for the Comp B melt-cast explosive to estimate effects of the loading pressure and the particle size of granular explosive component,and the mesoscopic model is validated against the experimental data.Further numerical simulations indicate that the initial density and formula proportion greatly affect the hot-spot ignition of melt-cast explosives.

A statistical model for predicting thermal chemical reaction rate

A simple model based on the statistics of individual atoms [Europhys. Lett. 94 40002 （2011）] or molecules [Chin. Phys. Lett. 29 080504 （2012）] was used to predict chemical reaction rates without empirical parameters, and its physical basis was further investigated both theoretically and via MD simulations. The model was successfully applied to some reactions of extensive experimental data, showing that the model is significantly better than the conventional transition state theory. It is worth noting that the prediction of the model on ab initio level is much easier than the transition state theory or unimolecular RRKM theory.

Rate Coecients and Kinetic Isotope E ects of Cl+XCl→XCl+Cl(X=H,D,Mu)Reactions from Ring Polymer Molecular Dynamics

The ring-polymer molecular dynamics(RPMD)was used to calculate the thermal rate coefficients and kinetic isotope effects of the heavy-light-heavy abstract reaction Cl+XCl→XCl+Cl(X=H,D,Mu).For the Cl+HCl reaction,the excellent agreement between the RPMD and experimental values provides a strong proof for the accuracy of the RPMD theory.And the RPMD results are also consistent with results from other theoretical methods including improved-canonical-variational-theory and quantum dynamics.The most novel finding is that there is a double peak in Cl+MuCl reaction near the transition state,leaving a free energy well.It comes from the mode softening of the reaction system at the peak of the potential energy surface.Such an explicit free energy well suggests strongly there is an observable resonance.And for the Cl+DCl reaction,the RPMD rate coefficient again gives very accurate results compared with experimental values.The only exception is at the temperature of 312.5 K,results from RPMD and all other theoretical methods are close to each other but slightly lower than the experimental value,which indicates experimental or potential energy surface deficiency.

Measurement of niobium reaction rate for material surveillance tests in fast reactors

A highly accurate and precise technique for measurement of the 93 Nb(n,n’)93m Nb reaction rate was established for the material surveillance tests,etc.in fast reactors.The self-absorption effect on the measurement of the characteristic X-rays emitted by 93m Nb was decreased by the dissolution and evaporation to dryness of niobium dosimeter.A highly precise count of the number of 93 Nb atoms was obtained by measuring the niobium solution concentration using inductively coupled plasma mass spectrometry.X-rays of 93m Nb were measured accurately by means of comparing the X-ray intensity of irradiated niobium solution with that of the solution in which stable 93 Nb was added.The difference between both intensities indicates the effect of 182 Ta,which is generated from an impurity tantalum,and the intensity of X-rays from 93m Nb was evaluated.Measurement error of the 93 Nb(n,n’)93m Nb reaction rate was reduced to be less than 4%,which was equivalent to the other reaction rate errors of dosimeters used for Joyo dosimetry.In addition,an advanced technique using Resonance Ionization Mass Spectrometry was proposed for the precise measurement of 93m Nb yield,and 93m Nb will be resonance-ionized selectively by discriminating the hyperfine splitting of the atomic energy levels between 93 Nb and 93m Nb at high resolution.

A QUANTITATIVE STUDY ON ENHANCEMENT OF TYPE Ⅱ PHOTOSENSITIZED OXIDATION REACTION RATE BY HEAVY WATER

A method for quantitative evaluating the enhancement of the rate of Type Ⅱ photosensitized oxidation by D_2O was suggested. The effect of substrate concentration on this process was also discussed.

Fusion Reaction Rate Coefficient for Different Beam and Target Scenarios

Fusion power output is proportional not only to the fuel particle number densities participating in reaction but also to the fusion reaction rate coefficient （or reactivity）, which is dependent on reactant velocity distribution functions. They are usuMly assumed to be dual Maxwellian distribution functions with the same temperature for thermal nuclear fusion circumstances. However, if high power neutral beam injection and minority ion species ICRF plasma heating, or multi-pinched plasma beam head-on collision, in a converging region are required and investigated in future large scale fusion reactors, then the fractions of the injected energetic fast ion tail resulting from ionization or charge exchange will be large enough and their contribution to the non-Maxwellian distribution functions is not negligible, hence to the fusion reaction rate coefficient or calculation of fusion power. In such cases, beam-target, and beam-beam reaction enhancement effect contributions should play very important roles. In this paper, several useful formulae to calculate the fusion reaction rate coefticient for different beam and target combination scenarios are derived in detail

MCSCF STUDIES ON THE IRC AND REACTION RATE CONSTANTS FOR THE DEHYDROGENATION REACTION OF VINYL RADICAL

The transition state(TS) and Intrinsic Reaction Coordinate (IRC) for the titled reaction were traced by means of MCSCF/6-31G (210 configurations). The reaction activation energy of this reaction is 140.2KJ/mol. The reaction rate constants of five temperetures were calculated by CVT involving the tunneling effects.

Molecular Orbital Nature of Solubility of Shot Chain n-Alkanes in Water and Their Reaction Rate Constants with Nitronium Cations: A DFT Study

The new theoretical models describe both the solubility S of the shot chain n-alkanes in water at 298.15 K, and their reaction rate constants k with nitronium cation NO2+ at 293.15 K on the basis of their molecular orbital characteristics. It is shown that both the quantities S and k are determined by the energies Eorb of the specific virtual (for S) and occupied (for k) molecular orbitals of these n-alkanes. The obtained regression equations confirm the theoretically found dependences of S and k on the absolute value of Eorb. This fact demonstrates that the electronic structure particularities of the studied n-alkanes play a crucial role in both their above-mentioned physicochemical properties.