Flame monitoring detector

The flame monitoring detector provides an on/off signal to indicate the presence or absence of flame within a designated space. The detector typically provides a signal relative to the intensity and distance between the flame and sensor. In the absence of the flame the detector will operate to shut down the boiler. 

Schematic diagram of a flame ionization detector. Ions and electrons formed in the flame provide an electrically conducting path between the flame at earth potential and an insulated cylindrical metal electrode at high potential. surrounding the flame the flow of current is monitored, amplified, and passed to the recording system.

Figure 14.14 Schematic diagram of the SFC olefins analyser system Cl, high-surface-area silica column C2, silver-loaded silica column VI and V2, six-poit valves FID, flame-ionisation detector UV, ulcaviolet monitor detector.

Figure 14.17 Schematic diagram of the on-line coupled LC-GC system VI, valve foi switcliing the LC column outlet to the GC injector V2, valve for switching the LC column to back-flush mode V3, LC injection valve RI, refractive index monitor detector UV, ulti avio-let monitor detector FID, flame-ionization detector.

Detectors. The function of the detector in HPLC is to monitor the mobile phase as it emerges from the column. The detection process in liquid chromatography has presented more problems than in gas chromatography there is, for example no equivalent to the universal flame ionisation detector of gas chromatography for use in liquid chromatography. Suitable detectors can be broadly divided into the following two classes ... 

Shinohara et al. [299] have described a procedure based on gas chromatography for the determination of traces of two, three, and five-ring azarenes in seawater. The procedure is based on the concentration of the compounds on Amberlite XAD-2 resin, separation by solvent partition [300], and determination by gas chromatography-mass spectrometry with a selective ion monitor. Detection limits by the flame thermionic detector were 0.5-3.0 ng and those by gas chromatography-mass spectrometry were in the range 0.02-0.5 ng. The preferred solvent for elution from the resin was dichloromethane and the recoveries were mainly in the range 89-94%. 

The chemiluminescent reaction with chlorine dioxide provides a highly sensitive and highly selective method for only two sulfur compounds, hydrogen sulfide and methane thiol [81]. As in the flame photometric detector (FPD), discussed below, atomic sulfur emission, S2(B3S -> ) is monitored in the wave-... 

Catalysts were tested for oxidations of carbon monoxide and toluene. The tests were carried out in a differential reactor shown in Fig. 12.7-1 and analyzed by an online gas chromatograph (HP 6890) equipped with thermal conductivity and flame ionization detectors. Gases including dry air and carbon monoxide were feed to the reactor by mass flow controllers, while the liquid reactant, toluene was delivered by a syringe pump. Thermocouple was used to monitor the catalyst temperature. Catalyst screening and optimization identified the best catalyst formulation with a conversion rate for carbon monoxide and toluene at room temperature of 1 and 0.25 mmolc g min1. Carbon monoxide and water were the only products of the reactions. 

Figure 3.15 A flame ionization detector. Hydrogen and oxygen are introduced into the gas mixture as it emerges from the column to allow it to be burnt in the detector. Some molecules are ionized in the flame and cause a current to flow between the two polarized electrodes. The degree of ionization varies with the composition of the gas mixture and the resulting changes in current can be monitored.

Fig. 4 Gas chromatographic traces of extracts from females of the pale brown chafer Phyl-lopertha diversa monitored by a conventional detector, flame-ionization detector (FID), and a biosensor, electroantennographic detector (EAD), using a male antenna as the sensing element. Although the peak of the sex pheromone (arrow) is hardly seen in the FID trace, its pheromonal activity was initially indicated by the strong EAD peak. Structural elucidation, followed by synthesis and behavioral studies lead to the identification of an unusual sex pheromone, l,3-dimethyl-2,4-(lff,3ff)-quinazolinedione [124]. It is unlikely that this minor compound would be fished out by a bioassay-oriented isolation procedure...

The available types of flame sensing detectors are ultraviolet (UV), infrared detection (IR), combination of these, and monitored closed circuit television (CCTV). These devices operate on the detection of certain wavelengths of light emitted by flames. They are used when there is a potential for fires that rapidly produce flame such as flash fire. 

Elemental composition H 5.92%, S 94.08. Hydrogen sulfide may be distinguished by its characteristic odor. The gas turns a paper soaked in lead acetate solution black. Many infrared sensors are commercially available for in-situ measurements of H2S. It may be monitored semiquantitatively by Draeger tubes. It also may be analyzed by GC following trapping over molecular sieves and thermal desorption. Either a flame photometric detector or a sulfur chemiluminescence detector may be used for GC analysis. It may be separated on a capillary column such as Carboxen 1006 PLOT or SPB-1 SULFUR (Supelco Catalog 1999 Supelco Inc., BeUefonte, PA). 

The gases exiting the reactor pass through a Beckman 565 infrared CO2 analyzer, which continuously monitored the production of carbon dioxide. Gas composition analysis was performed on-line using a Hewlett Packard 5890 II gas chromatograph, equipped with both a thermal conductivity and a flame ionization detector and a Porapak-Q column. Additional experimental details are given elsewhere (9). 

The direct gas-chromatographic method is especially suited as an analytical tool for enantiomer analysis when no sample derivatization is required. In the absence of diastereomeric effects between enantiomers ( EE-effect )25, the chiral compound may be investigated in situ, i.e., without isolation and purification using a minute amount of sample, e.g., by head-space analysis with 10 9 g using flame ionization detector (FID) or 1 (F 11 g using selected ion monitoring (GLC-MSSIM). 

TD-IT, Thermal desorption-ion trap CAD MIKE, collisionally activated decomposition mass-analyzed ion kinetic energy MID, multiple ion detection FID, flame ionization detector NPD, nitrogen/phosphorus detector SIM, selected ion monitoring El, electron impact TMS, trimethylsilane MTBSTFA, N-methyl-N-(tetr.-butyldimethylsilyl)trifluoroacetamide. 

Sensing Volume. The sensing volume of a sensor is the volume where the air is actually monitored. The sensing volume is the reaction chamber of a flame photometric detector or a chemiluminescence device, the field of view of an open-path sensor, or the White cell of a reduced-pressure optical system. The residence time of the sample within the sensing volume ultimately limits the temporal resolution of most chemical sensors. 

Reversed-phase HPLC has been used to analyze the oxidation products of triacylglycerols in edible oils. The detection is often based on monitoring the conjugated dienes with an ultraviolet detector (234-235 nm). However, the UV detector provides no information about oxidation products without a conjugated diene structure, e.g., products of oleic acid. Information about these compounds is important when oils with a high oleic acid content are studied. The most common universal detector types—refractive index and flame ionization detectors—are not sensitive enough to detect small amounts of oxidation products. 

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