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Detector Operation

Liquid chromatography was performed on symmetry 5 p.m (100 X 4.6 mm i.d) column at 40°C. The mobile phase consisted of acetronitrile 0.043 M H PO (36 63, v/v) adjusted to pH 6.7 with 5 M NaOH and pumped at a flow rate of 1.2 ml/min. Detection of clarithromycin and azithromycin as an internal standard (I.S) was monitored on an electrochemical detector operated at a potential of 0.85 Volt. Each analysis required no longer than 14 min. Quantitation over the range of 0.05 - 5.0 p.g/ml was made by correlating peak area ratio of the dmg to that of the I.S versus concentration. A linear relationship was verified as indicated by a correlation coefficient, r, better than 0.999. [Pg.395]

Fig. 4.7. A semiconductor detector operated as a pin diode with a reverse voltage or bias. An incident X-ray photon ultimately produces a series of electron-hole pairs. They are "swept out" by the bias field of-500 V- electrons in the direction ofthe n-layer holes in the direction ofthe p-layer. Thus, a small charge pulse is produced after [4.21],... Fig. 4.7. A semiconductor detector operated as a pin diode with a reverse voltage or bias. An incident X-ray photon ultimately produces a series of electron-hole pairs. They are "swept out" by the bias field of-500 V- electrons in the direction ofthe n-layer holes in the direction ofthe p-layer. Thus, a small charge pulse is produced after [4.21],...
Analysis and purification of the product solution is best accomplished by gas chromatography. The submitters used a 500 cm. by 0.6 cm. aluminum or polyethylene column packed with 21% oxydipropionitrile on Chromosorb P with column, injector and detector operated at 25° and a flow rate of 50 ml./minute. Under these conditions the retention times of bicyclopentene and cyclopentadiene were 3 and 5 minutes, respectively, beyond that of the coinjected air. Since bioyclo-pentene is extremely labile with respect to acid catalysis any contact with water, hydroxylic solvents, and nonprotic acids should be avoided (Note 11). Bicyclopentene stored at —78° in anhydrous tetrahydro-furan is stable indefinitely. [Pg.18]

The apparatus employed for this study was a Waters Associates Model ALC/GPC 300 with a differential refractometer as mass detector operated at room temperature. A 2 ml sample loop with polymer concentrations of 0.01-0.1 wt.% cUid a 5 ml siphon were employed with mobile phase flowrates in the reuige 1-8 ml/min. [Pg.268]

Eluent selection in ion chromatography is made more complex by the need to consider detector operating characteristics. [Pg.734]

A French Standard, which corresponds to ISO 10095 issued in 1992, specifies a method for determination of caffeine in green or roasted coffee or in coffee extracts (decaffeinated or not).33 Caffeine is extracted with water at 90°C in the presence of MgO. The extract is filtered, then cleaned-up on a mini-column packed with a silica phenyl group derivative, and analyzed by HPLC on a C18 column with a methanol/water (30 70) mobile phase and a UV detector operating at 254 to 280 nm. [Pg.34]

Which would be detected by an ec detector operating at a potential Et. [Pg.70]

This module describes the principles of radiation detection, detector operation, circuit operation, and specific radiation detector applications. [Pg.9]

Gas-filled detectors are used, for the most part, to measure alpha and beta particles, neutrons, and gamma rays. The detectors operate in the ionization, proportional, and G-M regions with an arrangement most sensitive to the type of radiation being measured. Neutron detectors utilize ionization chambers or proportional counters of appropriate design. Compensated ion chambers, BF3 counters, fission counters, and proton recoil counters are examples of neutron detectors. [Pg.41]

The liquid chromatograph Zarghi et al. used consisted of a Wellchrom K-1001 pump, Rheodyne 7125 injector, Eurochrom 2000 integrator, and K2600 fluorescence detector. The stationary phase was a Merck Chromolith Performance RP-18e column (100 x 4.6 mm). The mobile phase consisted of 0.01M dibasic sodium phosphate buffer and acetonitrile (60 40 v/v) adjusted to pH 3.5. The flow rate was 2 mL/min. The detector operated at an excitation wavelength of 240 nm and an emission wavelength of 340 nm. Letrozole served as the internal standard (IS). [Pg.303]

Ionization and condensation nuclei detectors alarm at the presence of invisible combustion products. Most industrial ionization smoke detectors are of the dual chamber type. One chamber is a sample chamber the other is a reference chamber. Combustion products enter an outer chamber of an ionization detector and disturb the balance between the ionization chambers and trigger a highly sensitive cold cathode tube that causes the alarm. The ionization of the air in the chambers is caused by a radioactive source. Smoke particles impede the ionization process and trigger the alarm. Condensation nuclei detectors operate on the cloud chamber principle, which allows invisible particles to be detected by optical techniques. They are most effective on Class A fires (ordinary combustibles) and Class C fires (electrical). [Pg.178]


See other pages where Detector Operation is mentioned: [Pg.1236]    [Pg.211]    [Pg.424]    [Pg.258]    [Pg.79]    [Pg.107]    [Pg.277]    [Pg.1623]    [Pg.208]    [Pg.428]    [Pg.135]    [Pg.139]    [Pg.143]    [Pg.146]    [Pg.156]    [Pg.282]    [Pg.297]    [Pg.657]    [Pg.668]    [Pg.669]    [Pg.728]    [Pg.812]    [Pg.955]    [Pg.242]    [Pg.327]    [Pg.158]    [Pg.35]    [Pg.76]    [Pg.55]    [Pg.40]    [Pg.135]    [Pg.59]    [Pg.137]    [Pg.191]    [Pg.303]    [Pg.86]    [Pg.282]    [Pg.306]    [Pg.229]   
See also in sourсe #XX -- [ Pg.2 , Pg.275 , Pg.294 , Pg.296 ]




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