Benches

The program storage requirements will depend somewhat on the computer and FORTRAN compiler involved. The execution times can be corrected approximately to those for other computer systems by use of factors based upon bench-mark programs representative of floating point manipulations. For example, execution times on a CDC 6600 would be less by a factor of roughly 4 than those given in the tcible and on a CDC 7600 less by a factor of roughly 24. 

The systems of such type have been developed of all last 10 years. We shall bring some characteristics of one of the last development within the framework of European BRITE project, carried out in LETT This 3D cone-beam tomograph is referred to as EVA Bench or Equipment for Voludensimetry Analysis. It is oriented on NDT of industrial products from ceramics and other composites. One of the main task of this tomograph is achievement of high resolution at study of whole internal volume of researched object. For test sample of the size 10mm spatial resolution in 50mm was obtained [14]. 

LETI. 3D cone-beam X-ray Tomograph EVA ( Equipment for Volumedensitometry Analysis) Bench, 1996. 

The obtained results for the magnetic bench have allowed to note that defects situated at 12 mm of depth have been observed clearly. This is explained by the high power furnished by the bench, in addition its induction is double alternation rectified. Dimensions of the defect (height and width) are precisely estimated (figure 1). The defect detection at this depth is due to the application of a rectified field, so skin phenomenon is almost absent. 

Measurement of the fatigue fractures depth during bench tests for crack resistance. 

The method is now applied to an object "o" consisting of an aluminum rod immersed in a tank and fixed at the supposed center of the bench the section of the rod being smaller than the central wavelength the size of the square section of the rod is 4 mm and the wavelength is 6 mm (the central frequency of the transducer is 250 kHz). Figure la gives the time-sinogram of the object without correction ... 

This paper intends to give, through different examples, guide-lines for characterization of array probes. We discuss, particularly, beam pattern measurement methods and raise the question whether it is useful to achieve a full characterization of all beams steered by the probe or to limit the characterization to a minimum set of acoustic configurations. An automatic bench for full characterization of tube inspection probes is described. 

Figure 4 Acoustic beam characterization set-up for the immersion SW array probe a/ Angle beam characterization principle b/ General view of the automatic bench...

Based on the results from the initial experiments ultrasonic equipment and transducers for the scanning system were selected. Also a measuring chamber with transducer fixtures was constructed and manufactured for measurement on the tubes directly on the drawing bench. 

Electrical noise (from the electronic control of the motors in the drawing bench) influenced the wall thickness measurements. 

In order to achieve the goals of making more efficient use of the information that is produced and of planning and performing better experiments, chemoinformatics will have to be more integrated into the daily work processes of the chemist, and into the work of the bench chemist. Certainly, many chemists still have to overcome high barriers to using the computer for assistance in the solution of their daily scientific problems. 

However, better use of spectral information for more rapid elucidation of the structure of a reaction product, or of a natural product that has just been isolated, requires the use of computer-assisted structure elucidation (CASE) systems. The CASE systems that exist now are far away from being routinely used by the bench chemist. More work has to go into their development. 

This does not have to be so Why not build an uninterrupted stream of information from the producer (the bench chemist) to the consumer (the reader of a journal or book, or the scientist that puts a query into a database) It is quite clear that the producers of information knows best what experiments were done, what observations were made, what results have been obtained. They should put this information into electronic laboratory books, augmented with spectral data (that they can obtain directly from the analytical laboratory). From this electronic repository aU other information sources -manuscripts, journals, books, databases - could be filled, clearly sometimes by manual selection, but not by changing data ... 

Fit securely to the lower end of the condenser (as a receiver) a Buchner flask, the side-tube carrying a piece of rubber tubing which falls well below the level of the bench. Steam-distil the ethereal mixture for about 30 minutes discard the distillate, which contains the ether, possibly a trace of unchanged ethyl benzoate, and also any biphenyl, CeHs CgHs, which has been formed. The residue in the flask contains the triphenyl carbinol, which solidifies when the liquid is cooled. Filter this residual product at the pump, wash the triphenyl-carbinol thoroughly with water, drain, and then dry by pressing between several layers of thick drying-paper. Yield of crude dry product, 8 g. The triphenyl-carbinol can be recrystallised from methylated spirit (yield, 6 g.), or, if quite dry, from benzene, and so obtained as colourless crystals, m.p. 162. ... 

Cool the flask in ice-water and pour the ethereal solution into a mixture of about 6 ml. of dil. H2SO4 and 10 g. of crushed ice contained in a 50 ml. flask fitted for steam-distillation, taking care to leave behind any unchanged magnesium. Fit to the lower end of the condenser a small Buchner flask or boiling-tube with side-arm (45°) carrying a piece of rubber tubing which falls well below the level of the bench. 

Sand. Buckets of dry sand for fire-extinguishing should be available in the laboratory and should be strictly reserved for this purpose, and not encumbered with sand-baths, waste-paper, etc. Most fires on the bench may be quickly smothered by the ample use of sand. Sand once used for this purpose should always be thrown away afterwards, and not returned to the buckets, as it may contain appreciable quantities of inflammable, non-volatile materials e.g., nitrobenzene), and be dangerous if used a second time. 

The inflammable solvents most frequently used for reaction media, extraction or recrystallisation are diethyl ether, petroleum ether (b.p. 40-60° and higher ranges), carbon disulphide, acetone, methyl and ethyl alcohols, di-Mo-propyl ether, benzene, and toluene. Special precautions must be taken in handling these (and other equivalent) solvents if the danger of Are is to be more or less completely eliminated. It is advisable to have, if possible, a special bench in the laboratory devoted entirely to the recovery or distillation of these solvents no flames are permitted on this bench. 

Ether. The most satisfactory method for the removal of (diethyl) ether is either on a steam bath fed from an external steam supply or by means of an electrically-heated, constant-level water bath (Fig. 77, 5, 1). If neither of these is available, a water bath containing hot water may be used. The hot water should be brought from another part of the laboratory under no circumstances should there be a free flame under the water bath. It caimot be too strongly emphasised that no flame whatsoever may be present in the vicinity of the distillation apparatus a flame 10 feet away may ignite diethyl ether if a continuous bench top lies between the flame and the still and a gentle draught happens to be blowing in the direction of the flame. 

Solvents with boiling points below 90-95°. A steam bath or water bath should be employed. Alternatively, the apparatus of Fig. 77,13, 3, but with a Alter flask as receiver, may be used the end of the rubber tubing attached to the tubulure is either placed in the sink or allowed to hang over the bench. If a distillation is ultimately to be conducted in the flask from which the solvent is removed, the apparatus depicted in Fig. 77,13, 4 is recommended the distilling flask may be replaced by a Claisen flask or a Claisen flask with fractionating side arm, particularly if the subsequent distillation is to be conducted under diminished pressure. 

A similar apparatus, but without the advantage of the central ground joint is marketed under the name Buechner stable filter f (Fig. 11,35, 2, a) one method of use is shown in Fig. II, 35, 2, b. The Buechner stable filter is made of porcelain the filtrate is drawn off through a vacuum chamber below the perforated plate, the whole apparatus is supported by a cylindrical base, and sits firmly on the bench. The sizes of perforated plate available are 56, 91, 111, 126, 186, 241 and 308 mm. diameter respectively, and it would appear that these will... 

Attention is directed to the fact that ether is highly inflammable and also extremely volatile (b.p. 35°), and great care should be taken that there is no naked flame in the vicinity of the liquid (see Section 11,14). Under no circumstances should ether be distilled over a bare flame, but always from a steam bath or an electrically-heated water bath (Fig.//, 5,1), and with a highly efficient double surface condenser. In the author s laboratory a special lead-covered bench is set aside for distillations with ether and other inflammable solvents. The author s ether still consists of an electrically-heated water bath (Fig. 11, 5, 1), fitted with the usual concentric copper rings two 10-inch double surface condensers (Davies type) are suitably supported on stands with heavy iron bases, and a bent adaptor is fitted to the second condenser furthermost from the water bath. The flask containing the ethereal solution is supported on the water bath, a short fractionating column or a simple bent still head is fitted into the neck of the flask, and the stUl head is connected to the condensers by a cork the recovered ether is collected in a vessel of appropriate size. 

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