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Insertion, ultrasonic

This study detects the defect of the void and the exfoliation in the solid phase diffusion bonding interface of ductile cast iron and stainless steel with a nickel insert metal using ultrasonic testing method, and examine the influence of mutual interference of the reflectional wave both the defect and the interface. [Pg.834]

Fig.6 shows the pulse shape at lOMHz in each point in Fig 5. As for measurement dB is constant because the material of the incidence of ultrasonic wave. The pulse amplitude has changed according to the thickness of the insert metal. Moreover, the direction of the first part of the pulse waveis different according to the material of the incidence of ultrasonic wave. [Pg.836]

In an alternative design, the actual tip of the ultrasonic hom may be used as the working electrode after insertion of an isolated metal disc [77, 78 and 79]. With this electrode, known as the sonotrode, very high limiting currents are obtained at comparatively low ultrasound intensities, and diflflision layers of less than 1 pm have been reported. Furdiemiore, the magniPide of the limiting currents has been found to be proportional to D, enabling a parallel to be drawn with hydrodynamic electrodes. [Pg.1943]

Tlie most common ceU case and cover materials are nylon and st) T enic (ABS). After inserting the ceU element, with cov er attached, into the ceU case, cover and case are cemented. For nylon, a most satisfactory adlieswe is phenol For styrene copoltyiiers, either a solvent seal or an ultrasonic seal is effective (see Adhesives). [Pg.549]

In ICP-AES and ICP-MS, sample mineralisation is the Achilles heel. Sample introduction systems for ICP-AES are numerous gas-phase introduction, pneumatic nebulisation (PN), direct-injection nebulisation (DIN), thermal spray, ultrasonic nebulisation (USN), electrothermal vaporisation (ETV) (furnace, cup, filament), hydride generation, electroerosion, laser ablation and direct sample insertion. Atomisation is an essential process in many fields where a dispersion of liquid particles in a gas is required. Pneumatic nebulisation is most commonly used in conjunction with a spray chamber that serves as a droplet separator, allowing droplets with average diameters of typically <10 xm to pass and enter the ICP. Spray chambers, which reduce solvent load and deal with coarse aerosols, should be as small as possible (micro-nebulisation [177]). Direct injection in the plasma torch is feasible [178]. Ultrasonic atomisers are designed to specifically operate from a vibrational energy source [179]. [Pg.619]

The advantages of this screen filter, as cited by the authors, consist of its reusability, its standard 96-well format size, and its ability to be used whenever sample transfer or pipetting is needed. After usage, the screen filter can be easily cleaned by rinsing with water and methanol and additionally, by ultrasonication in water or methanol or other appropriate solution. The filter can be inserted into a plasma storage plate before sample transfer by the Tomtec Quadra used by the authors for automation. [Pg.49]

Insertion of nano-materials into mesoporous materials-. Ultrasonic radiation has been used for the insertion of amorphous nano-sized catalysts into the mesopores. [Pg.594]

Ultrasonic insertion an ultrasonic transducer (horn) vibrates the insert, which heats by vibrating against the plastic. The advantages and drawbacks of this process are ... [Pg.759]

An in vitro investigation into the bactericidal effects of a dental ultrasonic descaler on bacterial biofilms using Actinobacillus actinomycctcmcomitans and Porphyromonas gin-givalis has been reported [49]. Suspensions of the bacteria were subjected to the vibrations of a Cavitron PI insert for 2.5 and 5.0 min in an acoustically-simulated model substrate. A 60 % kill rate was achieved at a temperature of around 50 °C which constituted an alternative treatment for bacterial biofilms. This study suggested that a similar approach could be used in the clean-up of a range of biofQms considered to be the cause of a range of environmental hazards. [Pg.145]

In contrast ultrasonic insertion Fig. 5.50 is where a hole is pre-moulded in the plastic (slightly smaller than the metal insert) and the horn is used first to melt the plastic before driving the insert into place. [Pg.216]

Fig. 7.23. Radial ultrasonic emitters for insertion in flow reactors. Fig. 7.23. Radial ultrasonic emitters for insertion in flow reactors.
Procedure. The rock wafers were gently cleaned three successive times with methanol in an ultrasonic bath, dried and placed in the inert atmosphere box. Two wafers of each rock type were inserted horizontally in stainless steel holders and placed in linear polyethylene containers holding 150 ml of the appropriate prepared water. The wafers were allowed to equilibrate with the water for three days and then 5 X of tracer solution was added. The resultant solutions contained V/ 5x10 M of each element. The pH of each solution was measured before and after the addition of the tracer and did not change sign-... [Pg.228]

To explain the formation of the expected product of insertion into the H—Si bond of HSiEt3 in similar yields from different precursors, it was suggested that t-Bu2Si also arises by ultrasound-promoted lithio-dehalogenation of t-Bu2SiX2 (X = Cl, Br, I) see also Section II.E. This would represent the first example of a metal-promoted a-elimination of dihalosilanes. In a related study of the chemistry of diadamantylsilylene Ad2Si the reactive species formed from Ad2Sil2 upon treatment with lithium under ultrasonic irradiation was compared with that formed upon pyrolysis of a silirane, as shown in equations 36 and 3757. [Pg.2479]

Drill a hole (3mm i.d.) through a PYC rod (8mm o.d., 4cm long) and insert the GC rod (diameter = 3 mm, length = 5 cm) so that it fits tightly in the PVC rod, resulting in a GC disk electrode (Fig. 4.1). Polish the GC disk electrode surface with successively finer grades of sandpaper and diamond pastes, and finally with 0.3 pm alumina. Clean ultrasonically for at least 15 min. [Pg.994]

Fig. 3.1 Setting-up and tuning an ultrasonic bath for use in zinc insertion, (a) The ultrasonic bath immediately after switching on. Note the intense disturbance above each of the two transducers, (b) At this point, the surface of the water has settled, but the two positions of maximum agitation are still distinct, (c) Placing the empty flask in the bath results in a smooth water surface, apart from the point immediately above the second transducer, (d) Optimum conditions for ultrasonic zinc insertion are shown here, with a perfectly smooth water surface, and significant frothing in the reaction flask. Fig. 3.1 Setting-up and tuning an ultrasonic bath for use in zinc insertion, (a) The ultrasonic bath immediately after switching on. Note the intense disturbance above each of the two transducers, (b) At this point, the surface of the water has settled, but the two positions of maximum agitation are still distinct, (c) Placing the empty flask in the bath results in a smooth water surface, apart from the point immediately above the second transducer, (d) Optimum conditions for ultrasonic zinc insertion are shown here, with a perfectly smooth water surface, and significant frothing in the reaction flask.
A pair of rigid stainless-steel wire hook-like electrodes with a distance of 4 mm are adjusted to the artery by means of a rack and pinion gear manipulator. The artery is raised slightly away from the surrounding tissue. Isolation of the electrodes is achieved by the insertion of a small piece of parafilm under the artery. Blood flow is measured with an ultrasonic Doppler flowmeter (Transonic, Ithaca NY, USA) the flow probe (1RB) is placed proximal to the damaged area. [Pg.284]

The PET was commercial (0.18 mm) Kodak ESTAR film base. The PE was commercial (0.10 mm) high density (HD) PE. To eliminate surface contamination, the polymer samples were ultrasonically cleaned in a series of solvents (heptane, dichloromethane, ethanol and ethyl acetate) and dried in a dry nitrogen atmosphere in a glove bag attached directly around the insertion probe of the spectrometer. Immediately after drying, the polymer samples were inserted into the preparation chamber of the spectrometer where they were evacuated to 5 x 10 9 Torr. The polymer samples were than annealed (PET 90° C, PE 60° C) for several hours to drive off any residual solvent, water, or adsorbed gases. [Pg.434]


See other pages where Insertion, ultrasonic is mentioned: [Pg.321]    [Pg.496]    [Pg.1021]    [Pg.779]    [Pg.321]    [Pg.496]    [Pg.1021]    [Pg.779]    [Pg.838]    [Pg.838]    [Pg.48]    [Pg.763]    [Pg.191]    [Pg.546]    [Pg.226]    [Pg.61]    [Pg.313]    [Pg.393]    [Pg.395]    [Pg.7]    [Pg.316]    [Pg.296]    [Pg.42]    [Pg.246]    [Pg.495]    [Pg.141]    [Pg.2483]    [Pg.32]    [Pg.208]    [Pg.60]    [Pg.91]    [Pg.286]    [Pg.291]    [Pg.420]    [Pg.420]    [Pg.126]    [Pg.42]   
See also in sourсe #XX -- [ Pg.321 ]




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Ultrasonic inserts

Ultrasonic processes insertion

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