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S sampling

Fig. 2 X-ray refraction topographs of a series of /OyPOj/s samples of different impact energies. The total damage of the laminates is characterized by addition of all debonded layers of0° and 90° fiber direction. Fig. 2 X-ray refraction topographs of a series of /OyPOj/s samples of different impact energies. The total damage of the laminates is characterized by addition of all debonded layers of0° and 90° fiber direction.
Figure B2.1.4 Fluorescence upconversion spectrometer based on the use of off-axis elliptical reflectors for the collection and focusing of fluorescence. Symbols used el, c2, off-axis elliptical reflectors s, sample x, nonlinear crystal. (After Jimenez and Fleming [21].)... Figure B2.1.4 Fluorescence upconversion spectrometer based on the use of off-axis elliptical reflectors for the collection and focusing of fluorescence. Symbols used el, c2, off-axis elliptical reflectors s, sample x, nonlinear crystal. (After Jimenez and Fleming [21].)...
Keith, L. H., ed. Compilation ofEPA s Sampling and Analysis Methods, Lewis Boca Raton, 1996. [Pg.52]

At the other extreme of Distefano s sample problems, for the largest initial charge, the maximum-stiffness ratio is of the order of 1500, which is considered to be a relatively large value. In this case, more than 10,000 time steps are required to distih 90 percent of the initial change, and the problem is better handled by a stiff integrator. [Pg.1339]

Shannon s sampling theorem states that A funetion f t) that has a bandwidth is uniquely determined by a diserete set of sample values provided that the sampling frequeney is greater than 2uj, . The sampling frequeney 2tJb is ealled the Nyquist frequeney. [Pg.200]

Reagent delivery It is possible to add reagents to the sample while the experiment is running using the APTAC instrument. Sample venting The pressure in APTAC s sample eontainer ean be automatieally released and the material eolleeted into an external vessel. [Pg.933]

Analyte(s) Sample matrix Sample preparation" Eirst EC mode Subsequent EC mode(s) Detection" Reference... [Pg.255]

The standard deviation is the square root of the variance and is denoted by c (population) or S (sample). [Pg.93]

An extensive study by Blackman (3) and a recent study by Millikan and White (21) on the vibrational relaxation of 02 are shown in Figure 2. The impurity of Blackman s sample varied from 1-5%, but the bulk impurity was nitrogen. Blackman s data at lower temperatures are significantly different from Millikan and White s values. The latters data have the same temperature dependence as Equation 5 over the... [Pg.56]

Interpretation Using Euclidean distances, the difference between the vendor s samples shows up nicely. (See data file SIEVEl.dat if some samples... [Pg.220]

Lewera A, Inukai J, Zhou WP, Cao D, Duong HT, Alonso-Vante N, Wieckowski A (2007) Chalcogenide oxygen reduction reaction catalysis X-ray photoelectron spectroscopy with Ru, Ru/Se and Ru/S samples emersed from aqueous media. Electrochim Acta 52 5759-5765... [Pg.343]

Figure 4. Conversion-time curves on a regenerated 2NiSZ(s) sample obtained at intermitent reaction periods after which the flow of n-butane was stopped, leaving the catalyst at the reaction temperature under a 100 cm/min flow of He for a few minutes, and then resuming the flow of n-butane. The arrows indicate 15 (tl injections of 1-butene. Figure 4. Conversion-time curves on a regenerated 2NiSZ(s) sample obtained at intermitent reaction periods after which the flow of n-butane was stopped, leaving the catalyst at the reaction temperature under a 100 cm/min flow of He for a few minutes, and then resuming the flow of n-butane. The arrows indicate 15 (tl injections of 1-butene.
Fig. 15. Waveforms used for in vivo electrochemical analysis. A = chronoamperometry, B = double chronoamperometry (response = SI — S2), C = linear sweep, D = differential pulse (response = S2 — SI), S = sample window... Fig. 15. Waveforms used for in vivo electrochemical analysis. A = chronoamperometry, B = double chronoamperometry (response = SI — S2), C = linear sweep, D = differential pulse (response = S2 — SI), S = sample window...
LOD for parent and degradate(s) Sample size requirements Stability of analyte(s)... [Pg.842]

B = mean integration counts for the calibration standards S = sample weight or volume (g or L)... [Pg.1350]

For the DRIFTS study, the Nafion-Ti02 slurries were sonicated for 2 hours, dried at ambient conditions for 5 hr, and ground with a pestle and mortar until a fine powder catalyst was formed. 30 mg of the resulting catalysts were placed on top of 80 mg of inert CaF2 powder (325 mesh, Alfa Aesar) in a DRIFTS cell s sample holder. The sample holder was enclosed by a dome with two IR transparent ZnSe windows and a third CaF2 window for UV illumination. For the ATR study, the Nafion-Ti02 slurries, which were sonicated for two hours, were cast directly on the surface of the ATR ZnSe crystal to form a continuous solid film. The films were enclosed with a stainless steel cover equipped with a CaF2 window for UV illumination. [Pg.464]


See other pages where S sampling is mentioned: [Pg.355]    [Pg.355]    [Pg.202]    [Pg.344]    [Pg.497]    [Pg.802]    [Pg.1756]    [Pg.192]    [Pg.235]    [Pg.361]    [Pg.460]    [Pg.200]    [Pg.178]    [Pg.700]    [Pg.154]    [Pg.41]    [Pg.288]    [Pg.42]    [Pg.42]    [Pg.593]    [Pg.9]    [Pg.24]    [Pg.199]    [Pg.193]    [Pg.438]    [Pg.28]    [Pg.268]    [Pg.200]   
See also in sourсe #XX -- [ Pg.144 , Pg.487 ]




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Sample Problems on S-N Curves

Shannon’s sampling theorem

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