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101.
When a bubble reaches an air-liquid interface, it ruptures, projecting a multitude of tiny droplets in the air. Across the oceans, an estimated 1018 to 1020 bubbles burst every second, and form the so called sea spray, a major player in earth’s climate system. At a smaller scale, in a glass of champagne about a million bubbles nucleate on the wall, rise towards the surface and burst, giving birth to a particular aerosol that holds a concentrate of wine aromas. Based on the model experiment of a single bubble bursting in simple liquids, we depict each step of this effervescence, from bubble bursting to drop evaporation. In particular, we propose simple scaling laws for the jet velocity and the top drop size. We unravel experimentally the intricate roles of bubble shape, capillary waves, gravity, and liquid properties in the jet dynamics and the drop detachment. We demonstrate how damping action of viscosity produces faster and smaller droplets and more generally how liquid properties enable to control the bubble bursting aerosol characteristics. In this context, the particular case of Champagne wine aerosol is studied in details and the key features of this aerosol are identified. We demonstrate that compared to a still wine, champagne fizz drastically enhances the transfer of liquid into the atmosphere. Conditions on bubble radius and wine viscosity that optimize aerosol evaporation are provided. These results pave the way towards the fine tuning of aerosol characteristics and flavor release during sparkling wine tasting, a major issue of the sparkling wine industry. 相似文献
102.
103.
Gabrielse G Bowden NS Oxley P Speck A Storry CH Tan JN Wessels M Grzonka D Oelert W Schepers G Sefzick T Walz J Pittner H Hänsch TW Hessels EA;ATRAP Collaboration 《Physical review letters》2002,89(23):233401
Cold antihydrogen is produced when antiprotons are repeatedly driven into collisions with cold positrons within a nested Penning trap. Efficient antihydrogen production takes place during many cycles of positron cooling of antiprotons. A first measurement of a distribution of antihydrogen states is made using a preionizing electric field between separated production and detection regions. Surviving antihydrogen is stripped in an ionization well that captures and stores the freed antiproton for background-free detection. 相似文献
104.
Bearden IG Beavis D Besliu C Blyakhman Y Budick B Bøggild H Chasman C Christensen CH Christiansen P Cibor J Debbe R Enger E Gaardhøje JJ Hagel K Hansen O Holm A Holme AK Ito H Jakobsen E Jipa A Jørdre JI Jundt F Jørgensen CE Karabowicz R Keutgen T Kim EJ Kozik T Larsen TM Lee JH Lee YK Løvhøiden G Majka Z Makeev A McBreen B Mikelsen M Murray M Natowitz J Nielsen BS Norris J Olchanski K Olness J Ouerdane D Płaneta R Rami F Ristea C Röhrich D Samset BH Sandberg D Sanders SJ Sheetz RA Staszel P 《Physical review letters》2002,88(20):202301
We present charged-particle multiplicities as a function of pseudorapidity and collision centrality for the 197Au+197Au reaction at square root[s(NN)] = 200 GeV. For the 5% most central events we obtain dN(ch)/deta/(eta = 0) = 625+/-55 and N(ch)/(-4.7< or =eta < or =4.7) = 4630 +/- 370, i.e., 14% and 21% increases, respectively, relative to square root[s(NN)] = 130 GeV collisions. Charged-particle production per pair of participant nucleons is found to increase from peripheral to central collisions around midrapidity. These results constrain current models of particle production at the highest RHIC energy. 相似文献
105.
Guo JH Luo Y Augustsson A Rubensson JE Såthe C Agren H Siegbahn H Nordgren J 《Physical review letters》2002,89(13):137402
We use x-ray emission spectroscopy to examine the influence of the intermolecular interaction on the local electronic structure of liquid water. By comparing x-ray emission spectra of the water molecule and liquid water, we find a strong involvement of the a(1)-symmetry valence-orbital in the hydrogen bonding. The local electronic structure of water molecules, where one hydrogen bond is broken at the hydrogen site, is separately determined. Our results provide an illustration of the important potential of x-ray emission spectroscopy for elucidating basic features of liquids. 相似文献
106.
Balestra F Bedfer Y Bertini R Bland LC Brenschede A Brochard F Bussa MP Choi S Colantoni ML Dressler R Dzemidzic M Faivre JC Ferrero A Ferrero L Foryciarz J Fröhlich I Frolov V Garfagnini R Grasso A Heinz S Jacobs WW Kühn W Maggiora A Maggiora M Manara A Panzieri D Pfaff HW Piragino G Popov A Ritman J Salabura P Tchalyshev V Tosello F Vigdor SE Zosi G;DISTO Collaboration 《Physical review letters》2002,89(9):092001
Total and differential cross sections for the exclusive reaction pp-->pp rho observed via the pi(+)pi(-) decay channel have been measured at p(beam)=3.67 GeV/c. The observed total meson production cross section is determined to be (23.4+/-0.8+/-8) mu b and is significantly lower than typical cross sections used in model calculations for heavy-ion collisions. The differential cross sections measured indicate a strong anisotropy (approximately cos(theta(CM)(rho)) in the rho(0) meson production. 相似文献
107.
108.
Manuel de Léon David Martín de Diego 《International Journal of Theoretical Physics》1996,35(5):975-1011
A classification of infinitesimal symmetries of singular autonomous and nonautonomous Lagrangian systems is obtained. The
relationship between infinitesimal symmetries and constants of the motion is given. 相似文献
109.
Marcel Baiwir Gabriel Llabrs Lon Christiaens Jean-Louis Piette 《Magnetic resonance in chemistry : MRC》1982,18(1):33-37
The 1H, 13C and 77Se chemical shifts have been measured for mononitrobenzo[ b ]selenophenes. For the homocyclic nuclei, the observed 1H- and 13C-values calculated from the empirical increments of nitrobenzene. Anomalous effects are observed in the 2- and 3-substituted derivatives and the nature of the Se? NO2 interactions in the former is discussed. 77Se chemical shifts of the 4-, 5- and 7-nitro derivatives are approximately correlated with the CNDO calculated electron densities; they also compare well with those of selenoanisoles and other phenyl alkyl selenides. The chemical shifts are also compared with the corresponding values in other heterocycles containing a selenophene moiety. 相似文献
110.