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Zero setting

High pressure bellows Restriction ring Center-stem assembly Zero-setting screw High pressure overload seal Range-spring assembly Torque-tube assembly... [Pg.23]

Repeat procedures (6) and (7) until full-scale deflection and zero settings are obtained. [Pg.728]

Sigma Zero Sets. Fits to Eq. (1) with Use of Values... [Pg.35]

If there is self-similarity in zero sets, the probability function is expressed by... [Pg.165]

When the rs-catastrophe surface is viewed from the side along lines of constant a, the outline is given by the equality of the two roots of the quadratic (19), i.e. the discriminant must be zero. Setting D in (20) equal to zero gives ... [Pg.291]

It is important to check the zero setting (or the setting of the lower range value) for an instrument as a zero error will cause the whole of the instrument span to be displaced. The zero setting may drift or change over a period of time (zero shift). Such drifting is frequently due to variations in ambient conditions—most commonly temperature. In addition to zero shift, point values of the measured variable in different regions of the span may drift by different amounts. [Pg.535]

System or Instrument Blank. It is a measure of system contamination and is the instrumental response in the absence of any sample. When the background signal is constant and measurable, the usual practice is to consider that level to be the zero setting. It is generally used for analytical instruments but is also applicable for instruments for sample preparation. [Pg.34]

Solvent/Reagent Blank. A solvent blank checks solvents and reagents that are used during sample preparation and analysis. Sometimes, a blank correction or zero setting is done based on the reagent measurement. For example, in atomic or molecular spectroscopy, the solvents and reagents used in sample preparation are used to provide the zero setting. [Pg.35]

Combination of Allocation Time with Zero Set up Time... [Pg.222]

Nonresonant part Instrumental response function and zero setting of delay time scale are provided. [Pg.27]

The isotropic signal delivers (rotation-free) information on the temporal evolution of the population numbers of the investigated vibrational transition(s). The induced dichroism is governed by the time constant ror (second-order reorientational correlation time, 1 = 2) and possibly population redistribution that may contribute to the loss of induced optical anisotropy. The zero-setting of the delay time scale (maximum overlap between pump and probing pulses) is determined by a two-photon absorption technique in independent measurements with an accuracy of better than 0.2 ps (67). [Pg.50]

Note Check the zero setting of the instrument frequently. [Pg.215]

Turn on the 02-electrode system and allow the circuitry to warm up or stabilize for 5 min. Check the operation of the recorder during this interval. Then set the recorder on pen and set the zero point adjustment control of the recorder to achieve a zero setting on the recorder during zero output from the 02-electrode system. This usually requires that you disconnect the 02-electrode system from the recorder or switch a zero output control on the 02-electrode system. [Pg.236]

In fc1 the only closed sets—zero sets of polynomials—are k1 itself and the finite sets. The topology is thus quite coarse it will not be Hausdorff, and the integers for instance are dense in the real line. But this is actually just what we want we will only be considering polynomial functions, and a real polynomial is indeed determined by its values on integers. More generally, the only maps

closed sets are the polynomial maps, where the coordinates of [Pg.38]

At the start of every experiment, the reactor was rinsed with Milli-Q water before zero-setting the analytical instrument. The reactor was then filled with the dye solution and it was ensured that no air bubbles remained in the system. The change in the dye concentration was continuously recorded. [Pg.176]

At the barrier height, the action in the reactive mode is equal to zero. Setting it to zero yields an expression for the energies of the quantized states sitting above the barrier. These are the gateway states. This expression is given by... [Pg.211]

At steady slate nothing varies with time, so that the derivative of Ca (and of every other system variable) with respect to time must equal zero. Setting dC /dt = 0 in the balance equation and letting Ca = Cas (steady stale) in the resulting equation yields... [Pg.553]

At equilibrium, the net rate of adsorption equals zero. Setting the right-hand side of Equation (10-4) equal to zero and solving for the concentration of CO adsorbed on the surface, we get... [Pg.596]

In fitting E(t) to a polynomial, one has to make sure that the polynomial does not become negative at large times. Another concern in the maximum mixedness calculations is that the term 1 —F k) does not go to zero. Setting the maximum value of F(t) at 0.999 rather than 1.0 will eliminate this problem. It can also be circumvented by integrating the polynomial for E t) to get F t) and then setting the maximum value of F t) at 0.999. [Pg.852]

Continue to read and record the absorbance of all the standard, blank and sample solutions. After every 10 absorbance readings, measure the absorbance of a standard check and use the zero check cuvette to check the zero setting. [Pg.91]

Manually or electronically construct a control chart. Label the y-axis cusum. Draw a horizontal hue at the midpoint of the y-axis to represent a cusum of zero. Set the range of values above and below to be about 10 times the standard deviation. Label the x-axis in terms of time, using day, run number, control obseiwation number, or whatever is most appropriate for recording the relative time of the control observation. [Pg.506]

A series of standard solutions are prepared and the intensity of emission determined for each concentration after zero setting of blank and hundred setting of the maximum concentration. The intensity of emissions from the test solutions is measured simultaneously and the concentration of the element is read from the calibration curve. [Pg.27]

Integration is relatively insensitive to noise, but is very sensitive to bias or offset, such as may result from an incorrect zero setting of the measuring instrument, or from some other phenomenon affecting the baseline. That integration is relatively insensitive to noise is readily seen when we consider noise in terms of its Fourier-analyzed components, i.e.,... [Pg.330]


See other pages where Zero setting is mentioned: [Pg.889]    [Pg.144]    [Pg.727]    [Pg.166]    [Pg.413]    [Pg.287]    [Pg.161]    [Pg.121]    [Pg.97]    [Pg.193]    [Pg.241]    [Pg.30]    [Pg.36]    [Pg.203]    [Pg.328]    [Pg.42]    [Pg.604]    [Pg.176]    [Pg.566]    [Pg.193]    [Pg.376]    [Pg.322]    [Pg.426]    [Pg.427]    [Pg.925]   
See also in sourсe #XX -- [ Pg.27 ]




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