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Detection, apparatus for

Dock, M., M. Fisher, and C. Cumming. Novel detection apparatus for locating underwater unexploded ordnance, in Proceedings of the 5th International Symposium on Technology and the Mine Problem, Mine Warfare Association, Monterrey, California, April 2002. [Pg.150]

Motored engine cool flames are discernible with the naked eye only with great difficulty, hence the reliance on detection apparatus for quantitative investigations. The essential features of radiation detection apparatus, such as shown in Figure 1, include a quartz window mounted in the combustion chamber, a photomultiplier radiation detector, and an amplifier-oscilloscope arrangement (107). [Pg.205]

Fig.4.60. Diagram of the reaction system and detection apparatus for HPLC of thioridazine and its metabolites. (From ref. 138 with permission of Preston Technical Abstracts Co., Niles, 111.)... Fig.4.60. Diagram of the reaction system and detection apparatus for HPLC of thioridazine and its metabolites. (From ref. 138 with permission of Preston Technical Abstracts Co., Niles, 111.)...
Let us consider the hyperfine depolarization effect caused by the presence of nuclear spin that is not oriented or aligned by light but acts as a randomly oriented flywheel to reduce the average polarization of fluorescence. The emission process can be effected by the presence of nuclear spin J, even if the hyperfine structure is unresolved by the detection apparatus. For this purpose one has to multiply each polarization moment fq in Eq. (5.34) by a coefficient g(K which is equal to [177, 402]... [Pg.173]

Fig. 5. Plan of the detection apparatus for measurement of the AWfi formation rate in... Fig. 5. Plan of the detection apparatus for measurement of the AWfi formation rate in...
FLOW SYSTEM AND DETECTION APPARATUS FOR CHEMILUMINESCENCE STUDIES... [Pg.247]

The detectable limits for a dispersion apparatus are a few g-g/g, and vary according to the environment around from a few pg/g for heavy elements in light matrices to a few mg/g for light elements. [Pg.34]

Figure B2.3.9. Schematic diagram of an apparatus for laser fluorescence detection of reaction products. The dye laser is syncln-onized to fire a short delay after the excimer laser pulse, which is used to generate one of the reagents photolytically. Figure B2.3.9. Schematic diagram of an apparatus for laser fluorescence detection of reaction products. The dye laser is syncln-onized to fire a short delay after the excimer laser pulse, which is used to generate one of the reagents photolytically.
Superfluid helium can pass easily through openings so small that they caimot be detected by conventional leak detection methods. Such leaks, permeable only to helium II, are called supedeaks. They can be a source of fmstrating difficulties in the constmction of apparatus for use with helium II. [Pg.8]

HCl aq EtOH). Recrystd from warm, acidified EtOH by addition of ammonia. The crude material (Ig) can be extracted with EtOH (50mL) in a Soxhlet apparatus for lOh to remove impurities. Impurities can be detected by paper electrophoresis. [Petrova et al. Anal Lett 5 695 1972.]... [Pg.330]

BS 50054 Electrical apparatus for the detection and measurement of combustible gases. General requirements and test methods Various... [Pg.364]

BS EN 45544 Electrical apparatus for the direct detection and measurement of toxic gases and vapours ... [Pg.364]

Apparatus. Set up the apparatus as in Section 14.10 with two small platinum plates connected to apparatus for the amperometric detection of the end point. [Pg.542]

The beating of a faint source with a high power coherent source is a well known process to detect its phase and amplitude. The same detection equipment allows the evaluation of the power of the source with theoretical limits similar to a noiseless photon counter. Such detection apparatus are limited by the bandwidth of the electronic component as this bandwidth is rapidly increasing, this may be a competitive solution for quantum limited detection in the far infra red. The phase of a thermal source is an useless information ... [Pg.372]

The first part of the book consists of a detailed treatment of the fundamentals of thin-layer chromatography, and of measurement techniques and apparatus for the qualitative and quantitative evaluation of thin-layer chromatograms. In situ prechromatographic derivatization techniques used to improve the selectivity of the separation, to increase the sensitivity of detection, and to enhance the precision of the subsequent quantitative analysis are summarized in numerous tables. [Pg.4]

Figure 4.6 shows an apparatus for the fluorescence depolarization measurement. The linearly polarized excitation pulse from a mode-locked Ti-Sapphire laser illuminated a polymer brush sample through a microscope objective. The fluorescence from a specimen was collected by the same objective and input to a polarizing beam splitter to detect 7 and I by photomultipliers (PMTs). The photon signal from the PMT was fed to a time-correlated single photon counting electronics to obtain the time profiles of 7 and I simultaneously. The experimental data of the fluorescence anisotropy was fitted to a double exponential function. [Pg.62]

To ensure that the detector electrode used in MEMED is a noninvasive probe of the concentration boundary layer that develops adjacent to the droplet, it is usually necessary to employ a small-sized UME (less than 2 /rm diameter). This is essential for amperometric detection protocols, although larger electrodes, up to 50/rm across, can be employed in potentiometric detection mode [73]. A key strength of the technique is that the electrode measures directly the concentration profile of a target species involved in the reaction at the interface, i.e., the spatial distribution of a product or reactant, on the receptor phase side. The shape of this concentration profile is sensitive to the mass transport characteristics for the growing drop, and to the interfacial reaction kinetics. A schematic of the apparatus for MEMED is shown in Fig. 14. [Pg.348]

An exeuaple of a nodular apparatus for capillary electrophoretic separation methods, is shown in Figure 4.43 [637-639,681-684]. It Offers a choice of automated sample introduction methods with on-column detection and has a... [Pg.265]

It is necessary to note that fluorescence characteristics demonstrate remarkable sensitivity to variations of physicochemical parameters of the environment. Therefore, such parameters as polarity, viscosity, temperature, electric potential, local electric field, pressure, pH, etc., can be registered successfully using the modem sensitive apparatus for fluorescence detection [1, 4—12]. As a consequence, fluorescent molecules are used successfully as molecular probes to study the local characteristics of physicochemical, biochemical and biological systems. [Pg.192]


See other pages where Detection, apparatus for is mentioned: [Pg.15]    [Pg.166]    [Pg.169]    [Pg.15]    [Pg.166]    [Pg.169]    [Pg.114]    [Pg.1824]    [Pg.473]    [Pg.1274]    [Pg.539]    [Pg.174]    [Pg.233]    [Pg.411]    [Pg.334]    [Pg.473]    [Pg.420]    [Pg.865]    [Pg.436]    [Pg.382]    [Pg.216]    [Pg.459]    [Pg.459]    [Pg.61]   
See also in sourсe #XX -- [ Pg.77 , Pg.81 ]




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