Guard detector

Small compressors will have motor overheat protection adjacent to the hermetic shell or built into the winding (see Section 4.8) and larger motors will have contactor-starters with overcurrent devices. Overheat protection is also fitted on many machines, to guard against high motor winding, cylinder head or oil temperatures. These usually take the form of thermistor detectors, connected to stop the motor. 

The Dionex system uses a Garbo Pac PA-1 anion exchange column and a CarboPac PA-1 Guard. The column was loaded with 25 pi of the RG solution and eluted with a linear gradient of 0 - 0.5 M NaOAc in 0.1 N NaOH during 50 minutes. The flow rate was 1.0 ml/min and the process was monitored using a PE detector. 

High Performance Liquid Chromatographic (HPLC) Analysis. A Waters HPLC system (two Waters 501 pumps, automated gradient controller, 712 WISP, and 745 Data module) with a Shimadzu RF-535 fluorescence detector or a Waters 484 UV detector, and a 0.5 pm filter and a Rainin 30 x 4.6 mm Spheri-5 RP-18 guard column followed by a Waters 30 x 3.9 cm (10 pm particle size) p-Bondapak C18 column was used. The mobile phase consisted of a 45% aqueous solution (composed of 0.25% triethylamine, 0.9% phosphoric acid, and 0.01% sodium octyl sulfate) and 55% methanol for prazosin analysis or 40% aqueous solution and 60% methanol for naltrexone. The flow rate was 1.0 mL/min. Prazosin was measured by a fluorescence detector at 384 nm after excitation at 340 nm (8) and in vitro release samples of naltrexone were analyzed by UV detection at 254 nm. 

To operate the ion TOF spectrometer in the velocity mode, we adapted a single-stage TOF spectrometer as shown in Fig. 3, which consisted of a repeller, an extractor (and guard rings, not shown) and a free-drift tube. After laser ionization, ions are extracted towards the MCP detector. For an ion with an initial kinetic energy Do, the total flight time t can be written as... 

Bergstrom et al. [63] used HPLC for determination of penicillamine in body fluids. Proteins were precipitated from plasma and hemolyzed blood with trichloroacetic acid and metaphosphoric acid, respectively, and, after centrifugation, the supernatant solution was injected into the HPLC system via a 20-pL loop valve. Urine samples were directly injected after dilution with 0.4 M citric acid. Two columns (5 cm x 0.41 cm and 30 cm x 0.41 cm) packed with Zipax SCX (30 pm) were used as the guard and analytical columns, respectively. The mobile phase (2.5 mL/min) was deoxygenated 0.03 M citric acid-0.01 M Na2HP04 buffer, and use was made of an electrochemical detector equipped with a three-electrode thin-layer cell. The method was selective and sensitive for mercapto-compounds. Recoveries of penicillamine averaged 101% from plasma and 107% from urine, with coefficients of variation equal to 3.68 and 4.25%, respectively. The limits of detection for penicillamine were 0.5 pm and 3 pm in plasma and in urine, respectively. This method is selective and sensitive for sulfhydryl compounds. 

Anti-coincidence units are used to reduce the effects of external interferences. The detector is surrounded by a second guard detector, so that ionizing radiation from outside (e.g. cosmic rays) must active the outer detector before penetrating to the inner. A sample placed close to, or inside, the inner detector will activate that only. The anti-coincidence unit is arranged to accept only the latter noncoincident pulses from the measuring detector. 

In addition to the commercially available systems, several authors have described laboratory-built systems using commercially available components from companies such as Upchurch Scientific (Oak Harbor, WA). One of the first reported laboratory-built micro-bore HPLC systems was described by Simpson and Brown, which was a simple adaptation of a standard HPLC system to accept micro-bore columns built from guard columns. A complete system has been described based on dual microdialysis syringe pumps (CMA Microdialysis, Chelmsford, M A) or dual syringe pumps (Harvard Apparatus, Inc., Holliston, MA), a microinjection port, and a micro-column the latter components being obtained from Upchurch scientific (Figure 3.5). This system was coupled with a laser-induced fluorescence (LIF) detector and used to measure neuropeptides in sub-microliter samples. A further modification of this system was built to perform immunoaffinity isolations of biomedically important analytes from clinical samples. ... 

Aspirin and salicylic acid were eluted with a mobile phase of aqueous acetonitrile, acidified to pH 2.6, using orthophosphoric acid, at a flow rate of 1.5 ml/min. A UVA is detector was employed with a wavelength of 295 nm, 0.1 aufs sensitivity and a response time of 0.5sec. A 25 cm x 4 mm Lichrocart Cl 8 cartridge column with a guard column of the same material was used and the column temperature was maintained at 40 °C. 

An HPLC system, equipped with a Waters solvent delivery system (M-45), two PLgel 20 p,m Mixed-A columns (300 x 7.5 mm) with 20 p,m guard column (50 x 7.5 mm) (Polymer Laboratories, Amherst, MA) and a refractive index detector (model 2410) (Waters, Milford, MA), can be used to study the molecular size and size distribution (e.g. molecular weight and weight distribution) of starch. 

Glycerin is used in Nasonex primarily as a humectant. For its quantification, both capillary gas chromatography method and HPLC methods may be selected. The GC is equipped with a flame-ionization defector, a 0.53 mm x 30 m fused silica analytical column coated with 3.0-p,mG43 stationary phase, and a 0.53 mm x 5 m silica guard column deactivated with phenylmethyl siloxane. The carrier gas was helium with a linear velocity of about 35 cm/s. The injection port and detector temperature was maintained at 240 and 260°C, respectively. The injection mode is splitless. The column temperature is programmed to be maintained at about 40°C for 20 min, then to increase to 250°C at a rate of 10°C/min and to hold at 250°C for 15 min. 

Avicel RC and CL are water-dispersible, colloidal, microcrystalline cellulose products made for use in liquid preparations. Avicel RC and CL are coprocessed mixtures of microcrystalline cellulose and sodium carboxymethylcellulose. The amount of NaCMC can be determined using the IC method. About 10 g of Nasonex and about 25 mg of NaCMC NF are separately refluxed with 30 mL of glacial acetic acid for 2 h. The refluxed mixture is transferred to a 100-mL volumetric flask and diluted to volume with purified water, and mixed. The ion chromatograph (IC) was equipped with a suppressed conductivity detector, a 4-mm CSRS suppressor, current at 50 mA, a 250 mm x 4-mm Ion CS 12A column and a 50 mm x 4 mm Ion CG 12A guard column. The mobile phase is 0.13% methanesulfonic acid in water with a flow rate of 1 mL/min. Equal... 

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