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1.
Raimo Vuopionperä 《Zeitschrift fur Physik C Particles and Fields》1995,65(2):311-325
The production of heavy Dirac and Majorana neutrinos ine + e ? collisions is investigated. The heavy Dirac and/or Majorana neutrinos can be produced in charged and neutral current processes $(e^ + e^ - \to N_1 \bar N_2 )$ . The production of a single heavy neutrino is possible if it mixes with the light neutrino species. The production of heavy neutrinos in Higgs channels is also studied, since in some specific models the Yukawa couplings could be large enough to make the production of heavy neutrinos through Higgs boson exchanges sufficiently large for detection. The most general left-right symmetric model with possibly complexV orA couplings is used in the analytic calculations of the production cross sections, but the numerical examples are given using simplified left-right symmetric model. The interference terms between different production channels have been studied in great detail and in some cases the interference terms are found to be non-negligible in wide range of production spectrum. The pair production cross section is larger in the Dirac case than it is in the Majorana case, but the single heavy Majorana neutrino production cross section is roughly twice as large as that of a Dirac neutrino. 相似文献
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An Experimental Study of the Kinetics of the Reactions of Isopropyl,sec‐Butyl,and tert‐Butyl Radicals with Molecular Chlorine at Low Pressures (0.5–7.0 Torr) in the Temperature Range 190–480 K 下载免费PDF全文
Timo T. Pekkanen Suula L. Arppe Arkke J. Eskola Matti P. Rissanen Raimo S. Timonen 《国际化学动力学杂志》2016,48(12):796-805
In this work, we have measured the rate coefficients of the reactions of isopropyl (propan‐2‐yl), sec‐butyl (butan‐2‐yl), and tert‐butyl (2‐methylpropan‐2‐yl) radicals with molecular chlorine as a function of temperature (190–480 K). The experiments were done in a tubular laminar flow reactor coupled to a photoionization quadrupole mass spectrometer employing a gas‐discharge lamp for ionization. The radicals were homogeneously produced in the reactor by photolyzing suitable precursor molecules with 193‐nm pulsed exciplex laser radiation. The bimolecular rate coefficients were obtained by monitoring the radical decay signals in real time under pseudo–first‐order conditions. The rate coefficients of all three reactions showed negative temperature dependence. The bath gas used in the experiments was helium, and the rate coefficients appeared to be independent of the helium concentrations employed ([2.4–14] × 1016 cm?3) for all three reactions. The rate coefficients of the reactions can be approximated in the studied temperature range by the following parameterizations: We estimate that the overall uncertainties of the measured rate coefficients are ±20%. We were able to observe 2‐chloropropane (i‐C3H7Cl) product for the i‐C3H7● + Cl2 reaction. No products were observed for the other two reactions, and the reasons for this are briefly discussed in the text. 相似文献
4.
We investigated the uptake of ethyl alcohol (ethanol) vapor by sulfuric acid solutions over the range approximately 40 to approximately 80 wt % H2SO4 and temperatures of 193-273 K. Laboratory studies used a fast flow-tube reactor coupled to an electron-impact ionization mass spectrometer for detection of ethanol and reaction products. The uptake coefficients (gamma) were measured and found to vary from 0.019 to 0.072, depending upon the acid composition and temperature. At concentrations greater than approximately 70 wt % and in dilute solutions colder than 220 K, the gamma values approached approximately 0.07. We also determined the effective solubility constant of ethanol in approximately 40 wt % H2SO4 in the temperature range 203-223 K. The potential implications to the budget of ethanol in the global troposphere are briefly discussed. 相似文献
5.
Tommi Kaplas Kari Laitinen Tuula Moilanen Yrj? Tolonen Kristoffer Albrecht Raimo Silvennoinen 《Optical Review》2010,17(3):252-256
Traditional Japanese woodblock printing is a centuries old art form. This time-honoured form of art is at risk of extinction
as a consequence of the increasing lack of availability of wild cherry trees, which are a traditionally used woodblock material.
Solutions for this material problem have been investigated for several years, but none of the tested materials has been sufficient
when compared with the watercolour print quality imprinted by wild cherry woodblocks. To contribute to overcoming this material
problem, we have investigated the physical properties of heat-treated woodblock materials made from different wood species.
The International Commission on Illumination (CIE) tristimulus values, the CIELAB coordinates, the total reflectance, and
the gloss, as well as, the water contact angle from the woodblock surface is observed to have a strong relation to the surface
treatment of a woodblock. The surface treatment of a woodblock, in turn, relates to its water delivery, which is the basis
for watercolour printing. 相似文献
6.
Arkke J. Eskola Timo T. Reijonen Timo T. Pekkanen Petri Heinonen Satya P. Joshi Raimo S. Timonen 《Proceedings of the Combustion Institute》2021,38(1):813-821
The kinetics of the i-C4H5 (buta-1,3-dien-2-yl) radical reaction with molecular oxygen has been measured over a wide temperature range (275–852 K) at low pressures (0.8–3 Torr) in direct, time-resolved experiments. The measurements were performed using a laminar flow reactor coupled to photoionization mass spectrometer (PIMS), and laser photolysis of either chloroprene (2-chlorobuta-1,3-diene) or isoprene was used to produce the resonantly stabilized i-C4H5 radical. Under the experimental conditions, the measured bimolecular rate coefficient of i-C4H5 + O2 reaction is independent of bath gas density and exhibits weak, negative temperature dependency, and can be described by the expression k3 = (1.45 ± 0.05) × 10?12 × (T/298 K)?(0.13±0.05) cm3 s?1. The measured bimolecular rate coefficient is surprisingly fast for a resonantly stabilized radical. Under combustion conditions, the reactions of i-C4H5 radical with ethylene and acetylene are believed to play an important role in forming the first aromatic ring. However, the current measurements show that i-C4H5 + O2 reaction is significantly faster under combustion conditions than previous estimations suggest and, consequently, inhibits the soot forming propensity of i-C4H5 radicals. The bimolecular rate coefficient estimates used for the i-C4H5 + O2 reaction in recent combustion simulations show significant variation and are up to two orders of magnitude slower than the current, measured value. All estimates, in contrast to our measurements, predict a positive temperature dependency. The observed products for the i-C4H5 + O2 reaction were formaldehyde and ketene. This is in agreement with the one theoretical study available for i-C4H5 + O2 reaction, which predicts the main bimolecular product channels to be H2CO + C2H3 + CO and H2CCO + CH2CHO. 相似文献
7.
Mikko Voutilainen Paul Sardini Marja Siitari-Kauppi Pekka Kek?l?inen Vesa Aho Markko Myllys Jussi Timonen 《Transport in Porous Media》2013,96(2):319-336
Numerical time-domain-diffusion simulations were used for studying the diffusion behavior of tracer molecules in rock matrix with homogeneous and heterogeneous porosity. As the heterogeneous sample in these simulations, a 3D tomographic image of altered tonalite was used, in which the mineral components and the pores resolved by X-ray microtomography were represented by their respective intragranular porosities determined previously by the 14C-PMMA method. The apparent diffusion coefficient of a tracer in altered tonalite was determined experimentally, and was then used in the simulations. In the altered tonalite analyzed, inclusion of heterogeneity in the porosity increased the diffusion coefficient by 16 %. Altered and pristine feldspar was the main mineral component in the sample (72 %), and it also provided the dominant contribution to tracer diffusion, explaining alone 52 % of the diffusion coefficient. The large pores resolved by microtomography (6 %) and altered and pristine mica (22 %) gave an equal contribution to the diffusion coefficient. The simulation method applied was also validated by comparing the results to both an analytical and a numerical solution to the diffusion equation in a homogenous medium. In addition, the method was compared to discrete-time random-walk simulations in the case of randomly placed overlapping spheres. 相似文献
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The kinetics of the C2H5 + Cl2, n‐C3H7 + Cl2, and n‐C4H9 + Cl2 reactions has been studied at temperatures between 190 and 360 K using laser photolysis/photoionization mass spectrometry. Decays of radical concentrations have been monitored in time‐resolved measurements to obtain reaction rate coefficients under pseudo‐first‐order conditions. The bimolecular rate coefficients of all three reactions are independent of the helium bath gas pressure within the experimental range (0.5–5 Torr) and are found to depend on the temperature as follows (ranges are given in parenthesis): k(C2H5 + Cl2) = (1.45 ± 0.04) × 10?11 (T/300 K)?1.73 ± 0.09 cm3 molecule?1 s?1 (190–359 K), k(n‐C3H7 + Cl2) = (1.88 ± 0.06) × 10?11 (T/300 K)?1.57 ± 0.14 cm3 molecule?1 s?1 (204–363 K), and k(n‐C4H9 + Cl2) = (2.21 ± 0.07) × 10?11 (T/300 K)?2.38 ± 0.14 cm3 molecule?1 s?1 (202–359 K), with the uncertainties given as one‐standard deviations. Estimated overall uncertainties in the measured bimolecular reaction rate coefficients are ±20%. Current results are generally in good agreement with previous experiments. However, one former measurement for the bimolecular rate coefficient of C2H5 + Cl2 reaction, derived at 298 K using the very low pressure reactor method, is significantly lower than obtained in this work and in previous determinations. © 2007 Wiley Periodicals, Inc. Int J Chem Kinet 39: 614–619, 2007 相似文献