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We introduce a new class of experiments which provide graphic insights into the propagation of acoustic waves in anisotropic media. Simply stated, we have devised a means of observing the expanding acoustic wavefront from a point disturbance in a solid. The data may be viewed as a movie or a series of snapshots. The observed wavefronts represent the group-velocity surfaces of acoustic waves, which reflect the basic elastic anisotropy of the solid. The technique has been applied to coherent acoustic waves with frequencies in the megahertz range (at ambient temperatures) and to incoherent heat pulses in the hundred-gigahertz range (at liquid-helium temperatures). In this article, we first provide a pedagogical introduction to wave propagation in elastically anisotropic media, reviewing some early methods for visualizing acoustic waves. Next, we describe the “acoustic wavefront imaging” method and give representative results in crystals and composite materials. Finally, we show how this method relates to recent advances in phonon imaging and internal diffraction of ultrasound. 相似文献
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Alexopoulos T Allen C Anderson EW Areti H Banerjee S Beery PD Biswas NN Bujak A Carmony DD Carter T Cole P Choi Y De Bonte RJ Erwin AR Findeisen C Goshaw AT Gutay LJ Hirsch AS Hojvat C Kenney VP Lindsey CS LoSecco JM McMahon T McManus AP Morgan N Nelson KS Oh SH Piekarz J Porile NT Reeves D Scharenberg RP Stampke SR Stringfellow BC Thompson MA Turkot F Walker WD Wang CH Wesson DK 《Physical review letters》1990,64(9):991-994
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Toward a microchip-based solid-phase extraction method for isolation of nucleic acids 总被引:7,自引:0,他引:7
Wolfe KA Breadmore MC Ferrance JP Power ME Conroy JF Norris PM Landers JP 《Electrophoresis》2002,23(5):727-733
A silica-based solid-phase extraction system suitable for incorporation into a microchip platform (nu-total analytical system; nu-TAS) would find utility in a variety of genetic analysis protocols, including DNA sequencing. The extraction procedure utilized is based on adsorption of the DNA onto bare silica. The procedure involves three steps: (i) DNA adsorption in the presence of a chaotropic salt, (ii) removal of contaminants with an alcohol/water solution, and (iii) elution of the adsorbed DNA in a small volume of buffer suitable for polymerase chain reaction (PCR) amplification. Multiple approaches for incorporation of this protocol into a microchip were examined with regard to extraction efficiency, reproducibility, stability, and the potential to provide PCR-amplifiable DNA. These included packing microchannels with silica beads only, generating a continuous silica network via sol-gel chemistry, and combinations of these. The optimal approach was found to involve immobilizing silica beads packed into the channel using a sol-gel network. This method allowed for successful extraction and elution of nanogram quantities of DNA in less than 25 min, with the DNA obtained in the elution buffer fraction. Evaluation of the eluted DNA indicated that it was of suitable quality for subsequent amplification by PCR. 相似文献
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Lazarus EA Navratil GA Greenfield CM Strait EJ Austin ME Burrell KH Casper TA Baker DR DeBoo JC Doyle EJ Durst R Ferron JR Forest CB Gohil P Groebner RJ Heidbrink WW Hong R Houlberg WA Howald AW Hsieh C Hyatt AW Jackson GL Kim J Lao LL Lasnier CJ Leonard AW Lohr J La Haye RJ Maingi R Miller RL Murakami M Osborne TH Perkins LJ Petty CC Rettig CL Rhodes TL Rice BW Sabbagh SA Schissel DP Scoville JT Snider RT Staebler GM Stallard BW Stambaugh RD St John HE Stockdale RE Taylor PL Thomas DM 《Physical review letters》1996,77(13):2714-2717
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