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61.
本文报道了多光束共振光压作用下钠原子束偏转的实验研究结果。文中提出了用多光束与原子束相互作用以增大原子束的偏转量,并可大大降低对激光功率的要求。用一台染料激光器照射钠原子束得到1×10-2rad的偏转角,偏转距离约7.2mm,并用激光诱导原子束荧光的方法检测原子束的偏转。 相似文献
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63.
Michael F. Vansco Kristen Zuraski Frank A. F. Winiberg Kendrew Au Nisalak Trongsiriwat Patrick J. Walsh David L. Osborn Carl J. Percival Stephen J. Klippenstein Craig A. Taatjes Marsha I. Lester Rebecca L. Caravan 《Molecules (Basel, Switzerland)》2021,26(10)
Methacrolein oxide (MACR-oxide) is a four-carbon, resonance-stabilized Criegee intermediate produced from isoprene ozonolysis, yet its reactivity is not well understood. This study identifies the functionalized hydroperoxide species, 1-hydroperoxy-2-methylallyl formate (HPMAF), generated from the reaction of MACR-oxide with formic acid using multiplexed photoionization mass spectrometry (MPIMS, 298 K = 25 °C, 10 torr = 13.3 hPa). Electronic structure calculations indicate the reaction proceeds via an energetically favorable 1,4-addition mechanism. The formation of HPMAF is observed by the rapid appearance of a fragment ion at m/z 99, consistent with the proposed mechanism and characteristic loss of HO2 upon photoionization of functional hydroperoxides. The identification of HPMAF is confirmed by comparison of the appearance energy of the fragment ion with theoretical predictions of its photoionization threshold. The results are compared to analogous studies on the reaction of formic acid with methyl vinyl ketone oxide (MVK-oxide), the other four-carbon Criegee intermediate in isoprene ozonolysis. 相似文献
64.
Meloni G Selby TM Goulay F Leone SR Osborn DL Taatjes CA 《Journal of the American Chemical Society》2007,129(45):14019-14025
The photoionization of 1-alkenylperoxy radicals, which are peroxy radicals where the OO moiety is bonded to an sp2-hybridized carbon, is studied by experimental and computational methods and compared to the similar alkylperoxy systems. Quantum chemical calculations are presented for the ionization energy and cation stability of several alkenylperoxy radicals. Experimental measurements of 1-cyclopentenylperoxy (1-c-C5H7OO) and propargylperoxy (CH2=C=CHOO) photoionization are presented as examples. These radicals are produced by reaction of an excess of O2 with pulsed-photolytically produced alkenyl radicals. The kinetic behavior of the products confirms the formation of the alkenylperoxy radicals. Electronic structure calculations are employed to give structural parameters and energetics that are used in a Franck-Condon (FC) spectral simulation of the photoionization efficiency (PIE) curves. The calculations also serve to identify the isomeric species probed by the experiment. Adiabatic ionization energies (AIEs) of 1-c-C5H7OO (8.70 +/- 0.05 eV) and CH2=C=CHOO (9.32 +/- 0.05 eV) are derived from fits to the experimental PIE curves. From the fitted FC simulation superimposed on the experimental PIE curves, the splitting between the ground state singlet and excited triplet cation electronic states is also derived for 1-c-C5H7OO (0.76 +/- 0.05 eV) and CH2=C=CHOO (0.80 +/- 0.15 eV). The combination of the AIE(CH2=C=CHOO) and the propargyl heat of formation provides Delta f H(0)(o) (CH2=C=CHOO+) of (1162 +/- 8) kJ mol-1. From Delta f H(0)(o) (CH2=C=CHOO+) and Delta f H (0)(o) (C3H3+) it is also possible to extract the bond energy D(0)(o)(C3H3+-OO) of 19 kJ mol-1 (0.20 eV). Finally, from consideration of the relevant molecular orbitals, the ionization behavior of alkyl- and alkenylperoxy radicals can be generalized with a simple rule: Alkylperoxy radicals dissociatively ionize, with the exception of methylperoxy, whereas alkenylperoxy radicals have stable singlet ground electronic state cations. 相似文献
65.
低温等离子体转化NO/O2/N2气氛中NO的实验研究 总被引:1,自引:0,他引:1
通过建立低温等离子体实验系统, 研究了介质阻挡放电型低温等离子体反应器作用于NO/O2/N2混合气体系时, NO, O2初始浓度对NO的转化效率的影响以及NOx, O3浓度随能量密度的变化关系. 低温等离子体作用于NO/O2/N2混合气体系时, NO同时发生氧化还原反应, 氧化反应占主导地位, 大部分NO转化为NO2; NO转化率随O2, NO初始浓度增大而降低, 能量密度在450~600 J/L时转化率较高; 产生的O3浓度随能量密度的增大呈先增后减的趋势. 相似文献
66.
RE Tribble A Azhari HL Clark CA Gagliardi Y-W Lui AM Mukhamedzhanov A Sattaroy X Tang L Trache V Burjan J Cejpek V Kroha S Piskor J Vincour F Carstoiu 《Pramana》1999,53(3):585-594
S-factors for direct capture reactions can be found at astrophysical energies from asymptotic normalization coefficients which
provide the normalization of the tail of the overlap function. For example the overlap for 8B → 7Be+p defines the S-factor for 7Be (p, γ)8B. Peripheral transfer reactions offer a technique to determine these asymptotic normalization coefficients. As a test of
the technique, the 16O(3He, d)17F reaction has been used to determine asymptotic normalization coefficients for transitions to the ground and first excited
states of 17F. The S-factors for 16O(p, γ)17F calculated from these 17F → 16O+p asymptotic normalization coefficients are found to be in very good agreement with recent measurements. Following the same
technique, the 10B(7Be, 8B)9Be and 14N(7Be, 8B)13C reactions have been used to measure the asymptotic normalization coefficient for 7Be(p, γ)8B. This result provides an indirect determination of S
17(0). 相似文献
67.
Dr. Edmond P. F. Lee Dr. Daniel K. W. Mok Prof. Dudley E. Shallcross Prof. Carl J. Percival Dr. David L. Osborn Prof. Craig A. Taatjes Prof. John M. Dyke 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(39):12411-12423
CH2OO, the simplest Criegee intermediate, and ozone are isoelectronic. They both play very important roles in atmospheric chemistry. Whilst extensive experimental studies have been made on ozone, there were no direct gas‐phase studies on CH2OO until very recently when its photoionization spectrum was recorded and kinetics studies were made of some reactions of CH2OO with a number of molecules of atmospheric importance, using photoionization mass spectrometry to monitor CH2OO. In order to encourage more direct studies on CH2OO and other Criegee intermediates, the electronic and photoelectron spectra of CH2OO have been simulated using high level electronic structure calculations and Franck–Condon factor calculations, and the results are presented here. Adiabatic and vertical excitation energies of CH2OO were calculated with TDDFT, EOM‐CCSD, and CASSCF methods. Also, DFT, QCISD and CASSCF calculations were performed on neutral and low‐lying ionic states, with single energy calculations being carried out at higher levels to obtain more reliable ionization energies. The results show that the most intense band in the electronic spectrum of CH2OO corresponds to the ${{\rm{\tilde B}}}$ 1A′ ← ${{\rm{\tilde X}}}$ 1A′ absorption. It is a broad band in the region 250–450 nm showing extensive structure in vibrational modes involving O–O stretching and C‐O‐O bending. Evidence is presented to show that the electronic absorption spectrum of CH2OO has probably been recorded in earlier work, albeit at low resolution. We suggest that CH2OO was prepared in this earlier work from the reaction of CH2I with O2 and that the assignment of the observed spectrum solely to CH2IOO is incorrect. The low ionization energy region of the photoelectron spectrum of CH2OO consists of two overlapping vibrationally structured bands corresponding to one‐electron ionizations from the highest two occupied molecular orbitals of the neutral molecule. In each case, the adiabatic component is the most intense and the adiabatic ionization energies of these bands are expected to be very close, at 9.971 and 9.974 eV at the highest level of theory used. 相似文献
68.
为了实现采摘机器人在复杂的自然场景下正确识别树上果实,来完成果实采摘,研究了不同环境下柑橘的识别方法.针对复杂的自然环境的影响及传统方法的局限性,在可见光和近红外区域择选5个特征波长滤波片,采集得到5幅滤波后的图像,并利用光谱角分类算法完成柑橘识别.试验结果表明,在光照角度、光照强度等不同条件下,柑橘的识别准确度达到96%.研究表明,滤波片光谱图像技术结合光谱角分类算法可以有效地识别自然场景下的成熟柑橘. 相似文献
69.
The objective of this study was to determine if topical anesthesia to the larynx and pharynx affects vocal fold motion during dynamic voice evaluation with transnasal flexible endoscopy. Transnasal dynamic laryngeal examinations of 10 patients with no voice complaints were evaluated by five blinded fellowship-trained laryngologists. Each patient was examined before and after application of topical anesthetic. Reviewers rated briskness of right and left vocal fold movement and longitudinal tension on a visual analogue scale. Statistical comparisons were made between individual subject scores before and after anesthetic application. Inter-rater reliability was also assessed. No statistical difference was observed between subject scores before and after anesthetic application. Average intraclass correlation coefficients were 0.643 and 0.591 for pre- and postanesthesia scores, respectively. Application of topical anesthesia to the larynx and pharynx does not affect vocal fold motion. 相似文献
70.