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Instrumental isolation

The phase relationship of each point of imbalance is the third factor that must be known. Balancing instruments isolate each point of imbalance and determine their phase relationship. Plotting each point of imbalance on a polar plot does this. In simple terms, a polar plot is a circular display of the shaft end. Each point of imbalance is located on the polar plot as a specific radial, ranging from 0 to 360°. [Pg.938]

Step 2. Instrumental isolation out of liquid culture media of individual cells. Step 3. Automated cell washing and cell suspension normalization to standard... [Pg.93]

There are, however, situations where classic strategies of thermodynamically controlled screening are difficult to apply. Many times, the complex libraries are difficult to analyze in spite of the progress in analysis techniques and instrumentation. Isolation of the amplified products is also... [Pg.173]

Using chemical or instrumental techniques, isolate X and X from all other elements in Y (not necessarily quantitatively) and measure the activity of X. Chemical isolation of the activity of interest is performed simply by separating it chemically from all other activities. Instrumental isolation of the activity of interest involves the detection of radiation that can uniquely identify the nuclide in question. [Pg.366]

Modern instruments isolate a narrow wavelength range of the spectrum for measurements. Those that use filters for this purpose are referred to as filter photometers those that use prisms or gratings are called spectrophotometers. Spectrophotometers are classified as being either single or double-beam. [Pg.64]

Proper isolation between the reactor signals and the computer must be ensured such that any malfunction in the computer is not transmitted to the reactor instrumentation. Isolation amplifiers are available commercially to provide full protection to channel output signals. Protection circuits may also be installed at the input to the interface card so as to avoid the possibility of any damage to the interface card and the computer. [Pg.5]

An added consideration is that the TOF instruments are easily and quickly calibrated. As the mass range increases again (m/z 5,000-50,000), magnetic-sector instruments (with added electric sector) and ion cyclotron resonance instruments are very effective, but their prices tend to match the increases in resolving powers. At the top end of these ranges, masses of several million have been analyzed by using Fourier-transform ion cyclotron resonance (FTICR) instruments, but such measurements tend to be isolated rather than targets that can be achieved in everyday use. [Pg.281]

When a system is isolated, it cannot be affected by its surroundings. Nevertheless, changes may occur within the system that are detectable with such measuring instruments as thermometers, pressure gauges, and so on. However, such changes cannot continue indefinitely, and the system must eventually reach a final static condition of internal equilibrium. [Pg.513]

Measuring process parameters on full-scale plants is notoriously difficult, but is needea for control. Usually few of the important variables are accessible to measurement. Recycle of material makes it difficult to isolate the effects of changes to individual process units in the circuit. Newer plants have more instrumentation, including on-line viscosimeters [Kawatra and Eisele, International ]. Mineral Processing, 22, 251-259 (1988)], mineral composition by on-line X-ray fluorescence, belt feeder weighers, etc., but the information is always incomplete. Therefore it is helpful to have models to predict quantities that cannot be measured while measuring those that can. [Pg.1839]

P IDs (piping and instrumentation diagrams) should identify instruments, sample locations, the presence of sample valves, nozzle blinding, and control points. Of particular importance are the bypasses and alternate feed locations. The isolation valves in these hues may leak and can distort the interpretation of the measurements. [Pg.2552]

The Q and ft) dependence of neutron scattering structure factors contains infonnation on the geometry, amplitudes, and time scales of all the motions in which the scatterers participate that are resolved by the instrument. Motions that are slow relative to the time scale of the measurement give rise to a 8-function elastic peak at ft) = 0, whereas diffusive motions lead to quasielastic broadening of the central peak and vibrational motions attenuate the intensity of the spectrum. It is useful to express the structure factors in a form that permits the contributions from vibrational and diffusive motions to be isolated. Assuming that vibrational and diffusive motions are decoupled, we can write the measured structure factor as... [Pg.479]

Of the instmments described only some are suitable for use outside the laboratory. Where any instrument is carried into a flammable environment it should either be certified as intrinsically safe for exposure to the flammable atmosphere or isolated from the atmosphere such as by keeping it within a purged enclosure. Any probe connected to the instmment must be separately considered as a possible ignition source. Electrometers are described in [ 1531. A more general review of electrostatic instruments is given in [ 136]. [Pg.50]

The linear power supply finds a very strong niehe within applieations where its ineffieieney is not important. These inelude wall-powered, ground-base equipment where foreed air eooling is not a problem and also those applieations in whieh the instrument is so sensitive to eleetrieal noise that it requires an eleetrieally quiet power supply—these produets might inelude audio and video amplifiers, RF reeeivers, and so forth. Linear regulators are also popular as loeal, board-level regulators. Here only a few watts are needed by the board, so the few watts of loss ean be aeeommodated by a simple heatsink. If dielee-trie isolation is desired from an ae input power souree it is provided by an ae transformer or bulk power supply. [Pg.11]

This power supply is going to provide power for a piece of process control instrument. The instrument receives its power from a +24 V bulk power supply which also provides transformer isolation from the input bus voltage to the unit. Please refer to Figure 3-66. [Pg.105]

With modern detectors and electronics most Enei -Dispersive X-Ray Spectroscopy (EDS) systems can detect X rays from all the elements in the periodic table above beryllium, Z= 4, if present in sufficient quantity. The minimum detection limit (MDL) for elements with atomic numbers greater than Z = 11 is as low as 0.02% wt., if the peaks are isolated and the spectrum has a total of at least 2.5 X 10 counts. In practice, however, with EDS on an electron microscope, the MDL is about 0.1% wt. because of a high background count and broad peaks. Under conditions in which the peaks are severely overlapped, the MDL may be only 1—2% wt. For elements with Z < 10, the MDL is usually around 1—2% wt. under the best conditions, especially in electron-beam instruments. [Pg.120]

Equipment technology and processing software for FTIR are very robust and provide a high degree of reliability. Concerns arise for only the most demanding applications. For quantitative work on an isolated feature in the spectrum, the rule of thumb is that the spectrometer resolution be one-tenth the width of the band. FTIR instruments routinely meet that requirement for solids. [Pg.424]

Although SFE and SFC share several common features, including the use of a superaitical fluid as the solvent and similar instrumentation, their goals are quite distinct. While SFE is used mainly for the sample preparation step (extraction), SFC is employed to isolate (chr-omatography) individual compounds present in complex samples (11 -15). Both techniques can be used in two different approaches off-line, in which the analytes and the solvent are either vented after analysis (SFC) or collected (SFE), or on-line coupled with a second technique, thus providing a multidimensional approach. Off-line methods are slow and susceptible to solute losses and contamination the on-line coupled system makes possible a deaease in the detection limits, with an improvement in quantification, while the use of valves for automation results in faster and more reproducible analyses (16). The off-line... [Pg.137]

Another way to improve the analysis of complex matrices can be the combination of a multidimensional system with information-rich spectral detection (31). The analysis of eucalyptus and cascarilla bark essential oils has been carried out with an MDGC instrument, coupling a fast second chromatograph with a matrix isolation infrared spectrometer. Eluents from the first column were heart-cut and transferred to a cryogenically cooled trap. The trap is then heated to re-inject the components into an analytical column of different selectivity for separation and subsequent detection. The problem of the mismatch between the speed of fast separation and the... [Pg.229]

Instruments with a balanced input circuit are available for measurements where both input terminals are normally at a potential other than earth. Further problems arise due to common-mode interference arising from the presence of multiple earth loops in the circuits. In these cases the instrument may need to be isolated from the mains earth. Finally, high-frequency instruments, unless properly screened, may be subject to radiated electromagnetic interference arising from strong external fields. [Pg.239]

The amplitude of each point of imbalance must be known to resolve dynamic balance problems. Most dynamic balancing machines or in situ balancing instruments are able to isolate and define the specific amount of imbalance at each point on the rotor. [Pg.938]

If s-l,2-divinylcyclobutane is desired, it can be isolated in 7—8% yield from the reaction mixture by preparative gas chromatography with the Beckman Megachrom instrument, using columns packed with Apiezon J. [Pg.67]


See other pages where Instrumental isolation is mentioned: [Pg.282]    [Pg.591]    [Pg.591]    [Pg.103]    [Pg.214]    [Pg.282]    [Pg.591]    [Pg.591]    [Pg.103]    [Pg.214]    [Pg.1349]    [Pg.374]    [Pg.388]    [Pg.201]    [Pg.313]    [Pg.235]    [Pg.465]    [Pg.938]    [Pg.504]    [Pg.59]    [Pg.61]    [Pg.223]    [Pg.535]    [Pg.252]    [Pg.281]    [Pg.393]    [Pg.31]    [Pg.122]    [Pg.24]    [Pg.69]    [Pg.432]    [Pg.241]    [Pg.653]   
See also in sourсe #XX -- [ Pg.93 ]




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