Sample tubes

The molar diamagnetic susceptibility of thiazole and some derivatives was initially determined by the classical Curie-Cheneveau method (5,315,316) and later confirmed by a method (317) based on the difference of NMR proton chemical shift of a sample of tetramethylsilane immersed in the liquid to be investigated, according to the shape (cylindrical or spherical) of the sample tube (Table 1-47) (318),... 

S ample Analysis. The fohowing procedure is used for sample analysis (/) after sample connections are made and the sample tubing purged for 30 minutes, the tubing is connected to the sampling manifold which serves to distribute sample gas to each of the analy2ers, and should analy2ers have specific pressure... 

Sampling from pneumatic conveyors parallels gas sampling. The exception is that soflds loadings can be as high as 50 kg of soHds per kg of gas. Commercially available samplers extract particles directly from a transport line. Fixed position samplers are mounted directly on the pneumatic conveyor pipe. Devices are available which extract samples from the product stream by the projection of a sample tube iato the flow. Particles impact on the tube and fill the open cavity. The tube is then withdrawn, and an internal screw discharges the collected material (20). In another model, the RX Sampler (manufactured by Gustafson) (29), samples are withdrawn usiag compressed air. 

Table 10.14 Thermal desorption of sorbed gas from sample tubes...

Elimination of sample preparation and handling of toxic solvents such as carbon disulphide Absence of solvent simplifies chromatograph Increased sensitivity Sample tubes can be reused ... 

A recovery of 5% of the total sample from the back-up section of charcoal in a sample tube was defined as the breakthrough point 50% of this value is shown as the recommended maximum tube loading, to allow for high humidity or the presence of other substances which reduce the normal tube capacity. 

B Sample Tube (A and B fixed in the focus points of the reflector)... 

When the burner went out, the solenoid valve took a few see-onds to elose, and during this time some oil entered the furnaee. In addition, the line between the last valve and the furnaee may have drained into the furnaee. The flash point of the fuel oil was 65°C, too high for the oil to be deteeted by the eombustible gas deteetor. Even though the oil was vaporized by the hot furnaee, it would have eondensed in the sample tube of the gas deteetor or on the sintered metal that surrounds the deteetor head. 

A useful device to have installed in a stirred autoclave is a liquid sampling tube by which liquid samples are withdrawn under pressure through a filter attached to the lower end of the tube. This device is especially useful for analysis of reaction progress and supplements information obtained from pressure-drop determinations. It is much easier to improve a less than satisfactory yield, if it can be determined what is going wrong and when. For academically orientated persons, a study of the rise and decline of various reaction products, as a function of reaction parameters and catalyst, can be a fertile source of useful publications. 

Cells used for high-temperature measurements in furnaces often consist of silica sample tubes, supported by thin vanadium sleeves. The key to the analysis is whether it is possible to have a container that scatters in a sufficiently predictable way, so that its background contribution can be subtracted. With the current neutron flux available from both pulsed and reactor sources, sample volumes of... 

The amount of rotation observed in a polarimetry experiment depends on the number of optically active molecules encountered by the light beam. This number, in turn, depends on sample concentration and sample pathlength. If the concentration of sample is doubled, the observed rotation doubles. If the concentration is kept constant but the length of the sample tube is doubled, the observed rotation is doubled. It also happens that the amount of rotation depends on the wavelength of the light used. 

A 1.20 g sample of cocaine, fa-]D = -16, was dissolved in 7.50 mLof chloroform and placed in a sample tube having a path length of 5.00 cm. What was the observed rotation ... 

In the 1H NMR spectrum, the acidic -C02H proton normally absorbs as a singlet near 12 5. As with alcohols (Section 17.11), the -C02H proton can be replaced by deuterium when D20 is added to the sample tube, causing the absorption to disappear horn the NMR spectrum. Figure 20.6 shows the H NMR spectrum of phenylacetic acid. Note that the carboxyl proton absorption occurs at 12.0 8. 

AOS surfactant concentration was 0.50% wt in deionized water. Aqueous phase pH was 8.5. The headspace was flushed with nitrogen. All samples were equilibrated at test temperature for 24 h prior to shaking the sample tubes for 1.0 min to generate the foam. Times given are elapsed time from the termination of foam generation. 

The second valve controls a sample loop, 5 cm long and 1 mm in diameter, packed with dimethyloctadecyl reverse phase comprising of fairly coarse particles 100-120 im in diameter to reduce flow impedance. The sample pump is supplied via a two-way tap from either of two reservoirs, one containing pure water and the other, normal saline. The output of the pump can be used to either force the contents of the open loop sample tube through the packed loop, or to permit washing with an appropriate solvent. The separate pump is necessary to overcome the impedance of the packed loop. 

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