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Ultrasonic Trapping In Capillaries For Trace-Amount Bi (Download Full Seminar Report)
Post: #1

Nonintrusive manipulation by standing-wave acoustics has been widely used for levitation and trapping of macroscopic objects.1 The standing-wave field creates an acoustic radiation force on the object that depends on its size and acoustic parameters.2 In the present article we demonstrate size-selective separation and retention of latex spheres inside a small-diameter flow-through capillary by use of an ultrasonic radiation trap. The work aims at rapid in-flow detection and separation of specific molecules via antibody-coated latex spheres. Acoustic radiation forces have been used for nonintrusive manipulation of macroscopic as well as microscopic objects. Basically, objects with higher acoustic impedance than the surrounding medium are trapped in the velocity antinodes of the standing-wave acoustic field. The theory of acoustic levitation and trapping is well understood.2,3 In aqueous solutions the method has been applied for studies of mechanical properties of mm- to mm-sized liquid droplets and biological cells.4,5¦..


http://www.http://pptpdf.net//?file=/computer%20science%20and%20electronics/ULTRASONIC-TRAPPING-IN-CAPILLARIES-FOR-TRACE-AMOUNT-B.pdf&name=ULTRASONIC-TRAPPING-IN-CAPILLARIES-FOR-TRACE-AMOUNT-B.pdf
Post: #2
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Sharon
Post: #3
abstract

In the small-diameter capillaries, there is a longitudinal semi-vertical vertical ultrasonic trap for the size-selective separation of the microscope. The trap uses the competition between the areas suspended in the liquid between the acoustic radiation force and the sticky drag forces between 20-75-M-fuse silica capillaries. Experiments used on 3.0- and 4.7-M-Latex regions demonstrated the principles of phosphate and verified the theoretically calculated size-dependent forces on the areas. The field showed by the use of laser-induced fluorescence. Its goal is to use the detection of proteins and other molecules to detect the separate and ultra-hydraulic sensitivity of two antigenic sites, by binding target molecules with high specificity for antibody-coated latex areas. © 2001 American Institute of Physics
 

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