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Analyzer Output

One needs to deploy an outlier- or fault-detection system, based on the analyzer outputs... [Pg.389]

Meanwhile operator A looked again at his 02 analyzer output, which showed 7.5 percent 02. He told operator B that there was plenty of oxygen because the analyzer showed 7.5 02, so he must be mistaken and, in fact, that he needed to go and pinch back still further on the air register to cut back the combustion air. [Pg.258]

The objectives of this study were twofold (1) to develop a new type of oxygen sensor which makes the crucible-type sensor more compact and which does not use air as a reference gas, (2) to analyze output characteristics of both the newly-developed zirconia oxygen sensor and the crucible-type oxygen sensor. [Pg.102]

The repeatability and short-term stability of the NDIR analyzers used at IMGC, i.e., Hartmann and Braun s URAS 10E, were tested in a previous work [1]. A procedure for calibrating NDIR analyzers with WRMs has been developed, which requires seven calibration points to establish the relationship between the analyzer output and the analyte concentration in the whole concentration range of interest. Since the traceability of measurements around the average C02 concentration is of particular... [Pg.226]

Fundamentally, EGA systems require powerful software control and data analysis systems, which, in addition to overall hardware control and displaying and analyzing output data, may also store reference libraries of MS or FTIR spectra to assist identification of the gaseous products of a thermal decomposition. However, EGA represents the most comprehensive group of thermoanalytical systems available for the characterization of the thermal behavior of materials. [Pg.3012]

ACIS measurements were performed at frequencies between 1 mHz and 1 kHz using a Solartron Model 1250 Frequency Response Analyzer. Output from the comb specimens was amplified with a Keithley Model 427 Current-to-Voltage Converter before waveform analysis. Reference electrodes were not used owing to the geometry of the encapsulated test specimens. The data reported herein were obtained with a 0.1 V rms amplitude sinusoidal excitation waveform. In one experiment, DC bias was superimposed on this waveform. [Pg.319]

Verification of Theory- The solid line in Figure 7 is the relative mass analyzer output plotted as a function of time for the 02-water depletion curve. The dotted line is the numerical evaluation of Equation 26 using the material properties published by Schuler and Kreuzer (II). Rib was determined to be 0.63 by the MTE equation. The initial deviations can arise from two sources. At t < 0, the ratio Rib is 0.68 owing to the reduced boundary layer from the added flow function. When the... [Pg.325]

The principal method of TS detection is based on the registration of the number of bursts (or waves) per second of the electrical signals. The electronic components include also a circuit to register the primary frequency components in the TS burst signal. The occurrence of the individual frequencies, is stored and recorded as a distribution versus frequency curve. The output curves are a scan of the TS activity versus temperature and the pulse height analyzer output that gives the density distribution per 1°C of TS activity. [Pg.736]

Whether we apply the above balancing procedure or not, the starting data required for the next step is a vector of fractional yields and conversions of components in the output. Many instruments will report the analyzed output composition in terms of mol fractions (or partial pressures) directly. However, as we saw in the above discussion, this raw data vector usually contains a composition that is not in atomic balance. The balancing described above produces the vector P which is a mass- and atomic-balanced vector but whose components do not add up to one and do not represent fractional conversions at the output. To get to that vector we need to renormalize the P vector by dividing each of its components by the sum of the components of p. The new vector P reports mol fractions at the output that are atomically balanced, but not the fractional conversions. We will call it a corrected composition vector. [Pg.153]

Structural constitution on a submicron scale as related to crystallinity, viz., crystalline unit cells, lamellae shape and size, and stress-induced shish kebab crystals. Computer system that stores, analyzes, and adjusts the controls of a machine based on the parameters established during the operation of the machine it is controlling. It continuously analyzes output data to adjust and maintain the machine s cycle within programmed limits. Can also store data and output it as directed by programming. [Pg.2238]

Key operating parameters should be checked and logged at least every 4 hr. Data logging may be automatic, but there should also be a system that ensures that operators have checked at least the on-line analyzer outputs and the key parameters listed below ... [Pg.1286]

Error messages could be in the form of a digital message (fully captured and archived), or a simple digital logic signal connected to the process controller receiving the analyzer output. [Pg.261]

Also the group of Olaj have performed quite a number of simulation studies, mainly on the kinetics of PLP. In a recent series of papers [172-174, 230] they have used a simulation method based on an iterative procedure [239-241]. The time interval is divided in small, equal intervals, each of duration kp [M]. The radical profile is then converged until a pseudo-steady-state profile is obtained, from which relevant kinetic data can then be calculated such as the rate of polymerization and / or the MWD. Olaj et al. [172-174, 230] used these kinetic data to explore the possibilities of recovering chain-length dependent termination rate coefficients from PLP experiments. In their simulations they compared the exact value of (which can be calculated in a simulation, but is not experimentally accessible) with the value of that they obtained from analyzing output data of their simulations, which are experimentally accessible parameters. In the case of using MWD data [172], the second moment of this distribution, according to [242-244] ... [Pg.51]

FIGURE 5 Geological sample, 400-s analysis. A multichannel analyzer output from a rock sample, using a 400-s counting time. Two spectra are compared dashed line is direct excitation using an Mo-anode tube dotted line is the same but using an Mo filter between tube and sample. [Pg.575]

Meanwhile operator A looked again at his analyzer output, which showed 7.5 percent O. He told operator B that there was plenty... [Pg.299]


See other pages where Analyzer Output is mentioned: [Pg.767]    [Pg.163]    [Pg.74]    [Pg.278]    [Pg.65]    [Pg.64]    [Pg.160]    [Pg.65]    [Pg.591]    [Pg.940]    [Pg.285]    [Pg.257]    [Pg.945]    [Pg.265]    [Pg.771]    [Pg.199]    [Pg.266]    [Pg.177]    [Pg.4769]    [Pg.688]    [Pg.53]    [Pg.56]    [Pg.56]    [Pg.56]    [Pg.153]    [Pg.300]   


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