Experimental Rate Coefficients Research Articles

Gas-Phase Phenyl Radical + O2 Reacts via a Submerged Transition State.

In the gas-phase chemistry of the atmosphere and automotive fuel combustion, peroxyl radical intermediates are formed following O2 addition to carbon-centered radicals which then initiate a complex network of radical reactions that govern the oxidative processing of hydrocarbons. The rapid association of the phenyl radical-a fundamental radical related to benzene-with O2 has hitherto been modeled as a barrierless process, a common assumption for peroxyl radical formation. Here, we provide an alternate explanation for the kinetics of this reaction by deploying double-hybrid density functional theory (DFT), at the DSD-PBEP86-D3(BJ)/aug-cc-pVTZ level of theory, and locate a submerged adiabatic transition state connected to a prereaction complex along the reaction entrance pathway. Using this potential energy scheme, experimental rate coefficients k(T) for the addition of O2 to the phenyl radical are accurately reproduced within a microcanonical kinetic model. This work highlights that purportedly barrierless radical oxidation reactions may instead be modeled using stationary points, which in turn provides insight into pressure and temperature dependence.

The temperature variation of the CH+ + H reaction rate coefficients: a puzzle finally understood?

CH+ was the first molecular ion identified in the interstellar medium and is found to be ubiquitous in interstellar clouds. However, its formation and destruction paths are not well understood, especially at low temperatures. A new theoretical approach based on the canonical variational transition state theory was used to study the H + CH+ reactive collisions. Rate coefficients for formation of C+ ions are calculated as a function of temperature. We considered the participation of a direct path and an indirect path in which the reactants should overcome an entropic barrier to form a van der Waals complex or pass through a CH2+ intermediate complex, respectively. We show that the contribution of both pathways to the formation of C+ has to be taken into account. The new reactive rate coefficients for the title reaction, complemented by reactive data for CH+/CH2+ in the H/H2/He mixture, have been used to simulate the corresponding kinetics experimentally measured using an Atomic Beam 22 Pole Trap apparatus at low temperature. A good agreement with the experimental findings was found at 50 K. At a lower temperature, the model overestimates the formation of C+. This shows that secondary reactions are not responsible for the weak C+ production in the experiments at such temperature. Then, we discuss the possible impact of non-adiabatic effects in the study of the H + CH+ reactive collisions and we found that such effects can be responsible for the decrease of the H + CH+ rate coefficients at low temperature. This study offers an explanation for the disagreement between H + CH+ theoretical and experimental rate coefficients which has been going on for 20 years and highlights the need for performing non-adiabatic studies for this simple chemical reaction.

Bimolecular Reaction of Methyl-Ethyl-Substituted Criegee Intermediate with SO2.

Methyl-ethyl-substituted Criegee intermediate (MECI) is a four-carbon carbonyl oxide that is formed in the ozonolysis of some asymmetric alkenes. MECI is structurally similar to the isoprene-derived methyl vinyl ketone oxide (MVK-oxide) but lacks resonance stabilization, making it a promising candidate to help us unravel the effects of size, structure, and resonance stabilization that influence the reactivity of atmospherically important, highly functionalized Criegee intermediates. We present experimental and theoretical results from the first bimolecular study of MECI in its reaction with SO2, a reaction that shows significant sensitivity to the Criegee intermediate structure. Using multiplexed photoionization mass spectrometry, we obtain a rate coefficient of (1.3 ± 0.3) × 10-10 cm3 s-1 (95% confidence limits, 298 K, 10 Torr) and demonstrate the formation of SO3 under our experimental conditions. Through high-level theory, we explore the effect of Criegee intermediate structure on the minimum energy pathways for their reactions with SO2 and obtain modified Arrhenius fits to our predictions for the reaction of both syn and anti conformers of MECI with SO2 (ksyn = 4.42 × 1011 T-7.80exp(-1401/T) cm3 s-1 and kanti = 1.26 × 1011 T-7.55exp(-1397/T) cm3 s-1). Our experimental and theoretical rate coefficients (which are in reasonable agreement at 298 K) show that the reaction of MECI with SO2 is significantly faster than MVK-oxide + SO2, demonstrating the substantial effect of resonance stabilization on Criegee intermediate reactivity.

Experimental and Theoretical Study of the Kinetics of the CH3 + HBr → CH4 + Br Reaction and the Temperature Dependence of the Activation Energy of CH4 + Br → CH3 + HBr.

The rate coefficient of the reaction of CH3 with HBr was measured and calculated in the temperature range 225-960 K. The results of the measurements performed in a flow apparatus with mass spectrometric detection agree very well with the quasiclassical trajectory calculations performed on a previously developed potential energy surface. The experimental rate coefficients are described well with a double-exponential fit, k1(exp) = [1.44 × 10-12 exp(219/T) + 6.18 × 10-11 exp(-3730/T)] cm3 molecule-1 s-1. The individual rate coefficients below 500 K accord with the available experimental data as does the slightly negative activation energy in this temperature range, -1.82 kJ/mol. At higher temperatures, the activation energy was found to switch sign and it rises up to about an order of magnitude larger positive value than that below 500 K, and the rate coefficient is about 50% larger at 960 K than that around room temperature. The rate coefficients calculated with the quasiclassical trajectory method display the same tendencies and are within about 8% of the experimental data between 960 and 300 K and within 25% below that temperature. The significant variation of the magnitude of the activation energy can be reconciled with the tabulated heats of formation only if the activation energy of the reverse CH4 + Br reaction also significantly increases with the temperature.

Machine learning rate constants of hydrogen abstraction reactions between ester and H atom

The rate constants of hydrogen abstraction reactions of alkyl ester by H atom are crucial for optimizing combustion reaction network and improving combustion efficiency of biodiesel. Due to the lack of experimental and theoretical rate coefficients data for some reactions - such as hydrogen abstraction of large biodiesel molecules by free radicals - machine learning provides a viable alternative to predict rate constants. In this study, three different machine learning (ML) methods - feedforward neural network (FNN), extreme gradient boosting (XGB) and XGB-FNN hybrid model - were used to predict rate constants of the reactions between alkyl ester and H atom. The rate constants of 41 reactions between H + CnH2n+1COOCmH2m+1 (n = 0–5, m = 1, 2) were calculated by the Master Equation System Solver (MESS) program over a temperature range of 300–2000 K for model training. The results showed that the XGB-FNN model with 8 descriptors has better overall performance than the other two ML methods. The average deviation of XGB-FNN model on the test set is 33.56% by performing leave one out (LOO) cross validations. The rate constants of the H + methyl decanoate (MD) reactions over a temperature range of 300∼2000 K were predicted by the XGB-FNN model, which follow well the modified three-parameter Arrhenius equation and agree well with theoretical values, indicating that the hybrid XGB-FNN model is robust in predicting the rate constants of alkyl ester and H atom in the temperature range of combustion. The present ML method in this study is supposed to be able to provide accurate and affordable rate constants prediction of larger systems, the molecular sizes of which are comparable to those of the dominant components of real biodiesel. That is important for the development of biodiesel kinetic models.

Hyperthermal Dynamics and Kinetics of the C(3P) + N2(X1Σg+) → CN(X2Σ+) + N(4S) Reaction

The hyperthermal dynamics and kinetics of the title reaction, which plays an important role in hypersonic chemistry for atmospheric entry vehicles, are investigated using quasi-classical trajectory methods on a recently developed ground electronic state potential energy surface. The dynamics calculations indicated that the reaction follows a complex-forming mechanism, despite its large endoergicity. The calculated differential cross section is forward-backward symmetric, consistent with a long-lived reaction intermediate supported by the NCN potential well. The lifetime of the reaction complex is sufficiently long that the vibrational distribution of the CN product can be predicted by the phase space theory. The calculated vibrational state specific and thermal rate coefficients follow the Arrhenius behavior, and the agreement with existing low-temperature experimental thermal rate coefficients is satisfactory. Extrapolations to high temperatures relevant to hypersonic conditions are provided.

Kinetics of IO radicals with C1, C2 aliphatic alcohols in tropospherically relevant conditions.

Kinetics of the reaction of IO radicals with methanol (MeOH) and ethanol (EtOH) were experimentally studied in the gas phase using pulsed laser photolysis-cavity ring-down spectroscopy (PLP-CRDS). IO radicals were produced in situ at the reaction zone by photolysing a mixture of precursors (CH3I + O3 + N2) at 248nm and thereby electronically excited at 445.04nm. The rate coefficients for the reactions of (IO + MeOH) and (IO + EtOH) were measured at a total pressure of 60Torr/N2 in the range of 258-360K. At room temperature, the experimental rate coefficients of the title reactions were measured to be [Formula: see text] and [Formula: see text]. Dependencies of the kinetics with photolysis laser fluence and experimental pressures were verified. Effects of pressure over the kinetic behaviour of the studied systems were observed to be insignificant within the statistical uncertainties when studied in the range of ~ 30-150Torr/N2, whereas a minor and linear fluence dependency was observed within the studied limit. From the measured kinetic parameters, the atmospheric lifetimes of MeOH and EtOH were calculated in the tropospherically relevant conditions regarding their reactions with important atmospheric oxidants like Cl atom, OH and IO radicals. To complement experimental results, kinetics and thermochemistry for the title reactions were investigated theoretically via canonical variational transition state (CVT) theory in combination with small curvature tunnelling (SCT) corrections with a dual-level Interpolated Single Point Energy (ISPE) approach at the CCSD(T)/def2-QZVPP//M06-2X/def2-TZVPP level of theory/basis set in the temperatures between 200 and 400K. Good degree of agreement was encountered between experimentally measured and theoretically calculated rate coefficients. This article also discusses the thermochemical parameters and kinetic branching ratios (BRs) of all the pathways involved in the title reactions.

Cost-Effective Implementation of Multiconformer Transition State Theory for Alkoxy Radical Unimolecular Reactions.

Alkoxy radicals are important intermediates in the gas-phase oxidation of volatile organic compounds (VOCs) determining the nature of the first-generation products. An accurate description of their chemistry under atmospheric conditions is essential for understanding the atmospheric oxidation of VOCs. Unfortunately, experimental measurements of the rate coefficients of unimolecular alkoxy radical reactions are scarce, especially for larger systems. As has previously been done for peroxy radical hydrogen shift reactions, we present a cost-effective approach to the practical implementation of multiconformer transition state theory (MC-TST) for alkoxy radical unimolecular (H-shift and decomposition) reactions. Specifically, we test the optimal approach for the conformational sampling as well as the best value for a cutoff of high-energy conformers. In order to obtain accurate rate coefficients at a reduced computational cost, an energy cutoff is employed to reduce the required number of high-level calculations. The rate coefficients obtained with the developed theoretical approach are compared to available experimental rate coefficients for both 1,5 H-shifts and decomposition reactions. For all but one of the reactions tested, the calculated MC-TST rate coefficients agree with experimental results to within a factor of 7. The discrepancy for the final reaction is about a factor of 15, but part of the discrepancy is caused by pressure effects, which are not included in MC-TST. Thus, for the fastest alkoxy reactions, deviation from the high-pressure limit even at 1 bar should be considered.

Investigation of the Gas-Phase Reaction of Nopinone with OH Radicals: Experimental and Theoretical Study

Monoterpenes are the most essential reactive biogenic volatile organic compounds. Their removal from the atmosphere leads to the formation of oxygenated compounds, such as nopinone (C9H14O), one of the most important first-generation β-pinene oxidation products that play a pivotal role in environmental and biological applications. In this study, experimental and theoretical rate coefficients were determined for the gas-phase reaction of nopinone with hydroxyl radicals (OH). The absolute rate coefficient was measured for the first time using a cryogenically cooled cell along with the pulsed laser photolysis–laser-induced fluorescence technique at 298 K and 7 Torr. The hydrogen abstraction pathways were found by using electronic structure calculations to determine the most favourable H-abstraction position. Pathway 5 (bridgehead position) was more favourable, with a small barrier height of −1.23 kcal/mol. The rate coefficients were calculated based on the canonical variational transition state theory with the small-curvature tunnelling method (CVT/SCT) as a function of temperature. The average experimental rate coefficient (1.74 × 10−11 cm3 molecule−1 s−1) was in good agreement with the theoretical value (2.2 × 10−11 cm3 molecule−1 s−1). Conclusively, the results of this study pave the way to understand the atmospheric chemistry of nopinone with OH radicals.

Shock tube study of the pyrolysis kinetics of Di- and trimethoxy methane

The high potential of oxymethylene ethers (OMEs) and related compounds as fuels and fuel-additives motivated a multitude of experimental and theoretical investigations on, e.g., dimethoxy methane (DMM), the smallest member of the OME family. The present work adds to this research by providing combined experimental and theoretical rate coefficients for di- and trimethoxy methane (TMM) pyrolysis. For DMM pyrolysis, the branching ratios between the major dissociation pathways remained elusive in recent studies and is elucidated in the present work using four independent sets of shock tube experiments and master equation modeling. For TMM pyrolysis, the present work provides the very first detailed chemical kinetics model. A key consumption reaction of both compounds, DMM and TMM, is the methoxy-induced H-atom migration, which yields methanol and a singlet diradical. While for DMM this reaction is in direct competition to the C–O bond fission reactions, TMM is found to be a prime example for methoxy-induced H-atom migration, as its pyrolysis chemistry is exclusively governed by this reaction. With the present work, the details of DMM pyrolysis are elucidated and the foundation is laid for detailed chemical kinetics modeling of TMM.

Experimental and Theoretical Studies of Trans-2-Pentenal Atmospheric Ozonolysis

We investigated the kinetics, mechanism and secondary organic aerosols formation of the ozonolysis of trans-2-pentenal (T2P) using four different reactors with Fourier Transform InfraRed (FTIR) spectroscopy and Gas Chromatography (GC) techniques at T = 298 ± 2 K and 760 Torr in dry conditions. The rate coefficients and branching ratios were also evaluated using the canonical variational transition (CVT) state theory coupled with small curvature tunneling (CVT/SCT) in the range 278–350 K. The experimental rate coefficient at 298 K was (1.46 ± 0.17) × 10−18 cm3 molecule−1 s−1, in good agreement with the theoretical rate. The two primary carbonyls formation yields, glyoxal and propanal, were 57 ± 10% and 42 ± 12%, respectively, with OH scavenger compared to 38 ± 8% for glyoxal and 26 ± 5% for propanal without OH scavenger. Acetaldehyde and 2-hydroxypropanal were also identified and quantified with yields of 9 ± 3% and 5 ± 2%, respectively, in the presence of OH scavenger. For the OH production, an upper limit of 24% was estimated using mesitylene as OH tracer. Combining experimental and theoretical findings enabled the establishment of a chemical mechanism. Finally, the SOA formation was observed with mass yields of about 1.5%. This work provides additional information on the effect of the aldehyde functional group on the fragmentation of the primary ozonide.

Experimental dielectronic recombination rate coefficients for lithium-like 40Ca17+

The rate coefficients for dielectronic recombination (DR) of lithium-like 40Ca17+ ions with ∆n = 0 core excitations are derived from electron–ion recombination spectra measured with merged-beams method at the heavy-ion storage ring CSRm. The experimental DR spectrum, in the electron–ion collision energy range of 0 to 42 eV in the center-of-mass frame, comprises of all DR resonance peaks belong to the 2s 2 S 1/2 → 2p 2 P 1/2, 3/2 core excitations. The resonant energies and strengths for the resolved resonances in 2pjnl series are determined by fitting of the measured DR peaks. The further interpretation of the measured DR rate coefficients has been performed by calculating the DR rate coefficients with relativistic configuration-interaction method implemented in flexible atomic code (FAC) and compared with the experimental results. The experimental results and FAC calculations are found to be in a good agreement within the experimental uncertainties. Moreover, temperature dependent plasma rate coefficients were constructed from 4 × 103 to 1 × 107 K energy region by convoluting experimental and theoretical DR rate coefficients with the Maxwellian energy distribution function and then compared with previously available data. The plasma DR rate coefficient is found to be significantly underestimated by the early theoretical data calculated by Jacobs et al, and Mazotta et al in the low temperature. In contrast, a very good agreement has been found between the theoretical DR data of Gu and Colgan et al and the presently measured results at the low temperature region. Therefore, the results in this work composed of a bench-mark data set for plasma modeling at the photoionized temperature range. We have also provided a fit to our measured and theoretical plasma rate coefficients for low temperature plasma modeling.

Calculations of electron-impact excitation and dielectronic recombination rate coefficients of highly charged silicon ions

The rate coefficients for dielectronic recombination and electron-impact excitation processes with H-like to Be-like silicon ions (${\mathrm{Si}}^{13+}\text{\ensuremath{-}}{\mathrm{Si}}^{10+}$) are calculated using relativistic distorted-wave approach. The prominent $▵n=1$ and the weaker $▵n=2$ and 3 dielectronic recombination (DR) resonances with $K$-shell excitations are presented, and compared with the existing DR experimental rate coefficients of ${\mathrm{Si}}^{13+}, {\mathrm{Si}}^{12+}$, and ${\mathrm{Si}}^{11+}$ ions, it is found that the theoretical DR rate coefficients are in very good agreement with the experimental results. With the same approach, the direct and resonant electron-impact excitation (EIE) cross sections associated with $1s\ensuremath{-}{n}^{\ensuremath{'}}{l}^{\ensuremath{'}}$ core excitations are calculated for the ground states of ${\mathrm{Si}}^{13+}\text{\ensuremath{-}}{\mathrm{Si}}^{10+}$ ions and found in excellent agreement with the available experiment. Finally, we present the synthesized DR and EIE rate coefficients for the sum of all detected $(13+\ensuremath{\sim}10+)$ charge states of Si and these agree well with the experimental results.

The kinetics of the reactions of Br atoms with the xylenes: an experimental and theoretical study.

This work reports the temperature dependence of the rate coefficients for the reactions of atomic bromine with the xylenes that are determined experimentally and theoretically. The experiments were carried out in a Pyrex chamber equipped with fluorescent lamps to measure the rate coefficients at temperatures from 295 K to 346 K. Experiments were made at several concentrations of oxygen to assess its potential kinetic role under atmospheric conditions and to validate comparison of our rate coefficients with those obtained by others using air as the diluent. Br2 was used to generate Br atoms photolytically. The relative rate method was used to obtain the rate coefficients for the reactions of Br atoms with the xylenes. The reactions of Br with both toluene and diethyl ether (DEE) were used as reference reactions where the loss of the organic reactants was measured by gas chromatography. The rate coefficient for the reaction of Br with diethyl ether was also measured in the same way over the same temperature range with toluene as the reference reactant. The rate coefficients were independent of the concentration of O2. The experimentally determined temperature dependence of the rate coefficients of these reactions can be given in the units cm3 molecule-1 s-1 by: o-xylene + Br, log10(k) = (-10.03 ± 0.35) - (921 ± 110)/T; m-xylene + Br, log10(k) = (-10.78 ± 0.09) - (787 ± 92/T); p-xylene + Br, log10(k) = (-9.98 ± 0.39) - (956 ± 121)/T; diethyl ether + Br, log10(k) = (-7.69 ± 0.55) - (1700 ± 180)/T). This leads to the following rate coefficients, in the units of cm3 molecule-1 s-1, based on our experimental measurements: o-xylene + Br, k(298 K) = 7.53 × 10-14; m-xylene + Br, k(298 K) = 3.77 × 10-14; p-xylene + Br, k(298 K) = 6.43 × 10-14; diethyl ether + Br, k(298 K) = 4.02 × 10-14. Various ab initio methods including G3, G4, CCSD(T)/cc-pV(D,T)Z//MP2/aug-cc-pVDZ and CCSD(T)/cc-pV(D,T)Z//B3LYP/cc-pVTZ levels of theory were employed to gain detailed information about the kinetics as well as the thermochemical quantities. Among the ab initio methods, the G4 method performed remarkably well in describing the kinetics and thermochemistry of the xylenes + Br reaction system. Our theoretical calculations revealed that the reaction of Br atoms with the xylenes proceeds via a complex forming mechanism in an overall endothermic reaction. The rate determining step is the intramolecular rearrangement of the pre-reactive complex leading to the post-reactive complex. After lowering the relative energy of the corresponding transition state by less than 1.5 kJ mol-1 for this step in the reaction of each of the xylenes with Br, the calculated rate coefficients are in very good agreement with the experimental data.

Atmospheric Chemistry of 2-Amino-2-methyl-1-propanol: A Theoretical and Experimental Study of the OH-Initiated Degradation under Simulated Atmospheric Conditions.

The OH-initiated degradation of 2-amino-2-methyl-1-propanol [CH3C(NH2)(CH3)CH2OH, AMP] was investigated in a large atmospheric simulation chamber, employing time-resolved online high-resolution proton-transfer reaction-time-of-flight mass spectrometry (PTR-ToF-MS) and chemical analysis of aerosol online PTR-ToF-MS (CHARON-PTR-ToF-MS) instrumentation, and by theoretical calculations based on M06-2X/aug-cc-pVTZ quantum chemistry results and master equation modeling of the pivotal reaction steps. The quantum chemistry calculations reproduce the experimental rate coefficient of the AMP + OH reaction, aligning k(T) = 5.2 × 10–12 × exp (505/T) cm3 molecule–1 s–1 to the experimental value kexp,300K = 2.8 × 10–11 cm3 molecule–1 s–1. The theoretical calculations predict that the AMP + OH reaction proceeds via hydrogen abstraction from the −CH3 groups (5–10%), −CH2– group, (>70%) and −NH2 group (5–20%), whereas hydrogen abstraction from the −OH group can be disregarded under atmospheric conditions. A detailed mechanism for atmospheric AMP degradation was obtained as part of the theoretical study. The photo-oxidation experiments show 2-amino-2-methylpropanal [CH3C(NH2)(CH3)CHO] as the major gas-phase product and propan-2-imine [(CH3)2C=NH], 2-iminopropanol [(CH3)(CH2OH)C=NH], acetamide [CH3C(O)NH2], formaldehyde (CH2O), and nitramine 2-methyl-2-(nitroamino)-1-propanol [AMPNO2, CH3C(CH3)(NHNO2)CH2OH] as minor primary products; there is no experimental evidence of nitrosamine formation. The branching in the initial H abstraction by OH radicals was derived in analyses of the temporal gas-phase product profiles to be BCH3/BCH2/BNH2 = 6:70:24. Secondary photo-oxidation products and products resulting from particle and surface processing of the primary gas-phase products were also observed and quantified. All the photo-oxidation experiments were accompanied by extensive particle formation that was initiated by the reaction of AMP with nitric acid and that mainly consisted of this salt. Minor amounts of the gas-phase photo-oxidation products, including AMPNO2, were detected in the particles by CHARON-PTR-ToF-MS and GC×GC-NCD. Volatility measurements of laboratory-generated AMP nitrate nanoparticles gave ΔvapH = 80 ± 16 kJ mol–1 and an estimated vapor pressure of (1.3 ± 0.3) × 10–5 Pa at 298 K. The atmospheric chemistry of AMP is evaluated and a validated chemistry model for implementation in dispersion models is presented.

Substituent Effect in the Reactions between Criegee Intermediates and 3-Aminopropanol.

Via intramolecular H atom transfer, 3-aminopropanol is more reactive toward Criegee intermediates, in comparison with amines or alcohols. Here we accessed the substituent effect of Criegee intermediates in their reactions with 3-aminopropanol. Through real-time monitoring the concentrations of two Criegee intermediates with their strong UV absorption at 340 nm, the experimental rate coefficients at 298 K (100-300 Torr) were determined to be (1.52 ± 0.08) × 10-11 and (1.44 ± 0.22) × 10-13 cm3 s-1 for the reactions of 3-aminopropanol with (CH3)2COO (acetone oxide) and CH2CHC(CH3)OO (methyl vinyl ketone oxide), respectively. Compared to our previous experimental value for the reaction with syn-CH3CHOO, (1.24 ± 0.13) × 10-11 cm3 s-1, we can see that the methyl substitution at the anti position has little effect on the reactivity while the vinyl substitution causes a drastic decrease in the reactivity. Our theoretical calculations based on CCSD(T)-F12 energies reproduce this 2-order-of-magnitude decrease in the rate coefficient caused by the vinyl substitution. Using the activation strain model, we found that the interaction of Criegee intermediates with 3-aminopropanol is weaker for the case of vinyl substitution. This effect can be further rationalized by the delocalization of the lowest unoccupied molecular orbital for the vinyl-substituted Criegee intermediates. These results would help us better estimate the impact of similar reactions like the reactions of Criegee intermediates with water vapor, some of which could be difficult to measure experimentally but can be important in the atmosphere. We also found that the B2PLYP-D3BJ/aug-cc-pVTZ calculation can reproduce the CCSD(T)-F12 reaction barrier energies within ca. 1 kcal mol-1, indicating that the use of the B2PLYP-D3BJ method is promising for future predictions of the reactions of larger Criegee intermediates.

Dielectronic recombination in O4+ near the ionization threshold

Relativistic perturbation theory calculations are carried out for dielectronic recombination cross sections involving jj J levels near the ionization threshold. We included levels in the 1s 22p 23l, 1s 22s2p3l, 1s 22s2p4l, 1s 22s2p5l, and 1s 22s2p6l configurations of O3+ that lie within ±5.0 eV of the O4+ ionization threshold. Theoretical dielectronic recombination cross sections are compared with experimental dielectronic recombination rate coefficients from 0.0 eV to 5.0 eV above threshold.

10]annulene: Electrocyclization mechanisms.

The mechanism of 6-π electrocyclization of all-cis, mono-trans, and double-trans [10]annulene to yield 4a,8a-dihydronaphthalene has been explored at various quantum-chemical methods. The mono-trans configuration cyclizes preferentially to trans-4a,8a-dihydronaphthalene, in agreement with the experimental results. The cyclization of the all-cis configuration requires firstly a bond-shifting to the naphthalene-like conformation of double-trans [10]annulene, which is the rate-limiting step, and finally its azulene-like conformation electrocyclizes quickly to cis-4a,8a-dihydronaphthalene. Its experimental rate coefficient is consistent with the computed one for the cyclization of the all-cis configuration, unlike the calculated one for the double-trans configuration. These results confirm the configurations assigned by Masamune et al. to the two isomers which they isolated.

Quasi-classical trajectory investigation of H + SO2 → OH + SO reaction on full-dimensional accurate potential energy surface

The reaction H+SO2→OH+SO is important in the combustion and atmospheric chemistry, as well as the interstellar medium. It also represents a typical complex-forming reaction with deep complexes, serving as an ideal candidate for testing various kinetics theories and providing interesting reaction dynamical phenomena. In this work, we reported a quasi-classical trajectory study of this reaction on our previously developed accurate full-dimensional potential energy surface. The experimental thermal rate coefficients over the temperature range 1400 K≤T≤2200 K were well reproduced. For the reactant SO2 being sampled at the ground ro-vibrational state, the calculated integral cross sections increased slightly along the collision energy ranging from 31.0 kcal/mol to 40.0 kcal/mol, and then became essentially flat at the collision energy within 40.0−55.0 kcal/mol. The product angular distributions are almost symmetric with nearly identical backward-forward double peak structure. The products OH and SO vibrational state distributions were also analyzed.

Performance of West African dwarf goats fed supplemented with Myrianthus arboreus leaf meal concentrates

A feeding trial was conducted to evaluate the performance of West African Dwarf goats fed Panicum maximum supplemented with Myrianthus arboreus leaf meal for 49 days. Four diets were formulated such that diet A contained 0.00% Myrianthus arboreus, diet B contained 10.00% Myrianthus arboreus, diet C contained 11.00% Myrianthus arboreus and diet D contained 12.00% Myrianthus arboreus respectively. A total of twelve (12) West African Dwarf goats were randomly allocated to the four diets with three animals per diet, each serving as a replicate. Parameters assessed were the chemical composition of the experimental diets, growth rate and digestibility coefficient of the animals. The results showed that diet D had the highest dry matter (92.55%) and crude protein (20.55%) contents. The average daily weight gain (g/day) of animals was significantly (P<0.05) nfluenced across the treatments. Animals fed diet D recorded the highest weight gain (19.39g/day) while the least weight gain (7.55g/day) was recorded for animals on diet B. The highest total dry matter intake (340.34g/day) was recorded for animals on diet D while the least (313.18g/day) was observed in animals fed diet C. The best feed conversion ratio(17.55) was recorded in animals fed diet D. There were significant differences (P<0.05) in the nutrient digestibility of the experimental animals. The highest dry matter (82.70%), crude protein (86.18%) digestibilities were observed in diet D while the least dry matter digestibility (72.73%) was observed in diet B. However, the least fibre fractions digestibilities were observed in diet D. It can therefore be concluded that supplementation of Myrianthus arboreus leaf meal concentrate at 12% inclusion with Panicum maximum as basal diet for goats can enhance nutrient digestibility and improve growth without any deleterious effects on the animals.