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D measurements

Following Bradshaw [17], we can give the definition of a similarity measure as follows Consider two objects A and B, a is the number of features (characteristics) present in A and absent in B, b is the number of features absent in A and present in B, c is the number of features common to both objects, and d is the number of features absent from both objects. Thus, c and d measure the present and the absent matches, respectively, i.e., similarity while a and b measure the corresponding mismatches, i.e., dissimilarity. The total ntunber of features is n = a + b + c + d. [Pg.304]

Carlson, F.E., Phillips, E.K., Tenhaeff, S.C. and Detlefsen, W.D., Measuring and Controlling Volatile Organic Compound and Paniculate Emissions from Wood Processing Operations and Wood-Based Products. Forest Products Society, Madison WI, 1995, pp. 52-61. [Pg.942]

Gettleman, L., Cocks, F. H., Darmiento, L. A., Levine. P. A., Wright, S. and Nathanson, D. Measurement of In Vivo Corrosion Rates in Baboons and Correlation with In Vitro Tests , Journal of Dental Research, 59, 689-707 (1980)... [Pg.466]

Strictly the diffusion coefficient D measured for any type of binary system A/B is in fact the resultant effect of two partial diffusivities and D, representing respectively the diffusivity of A into B and of B intO/4. For most practical purposes, however, a single diffusion coefficient is sufficient to define a given diffusion system. [Pg.399]

SCF calculations have been carried out on /V,/V-dicthylcyclopent[c]azepin-3-amine and a dipole moment of 3.70 D measured.1... [Pg.116]

Encycl 6, E173-L details a literature method for detg w in NC and proplnts thru the use of dry K carbonate pumice to absorb w in a gravimetric procedure, Encycl 6, E176-R describes a differential d measurement of the solvents used in proplnt manuf for the detn of ale, eth w (Ref 2). Other older gravimetric methods are given in Refs 1, 3 4... [Pg.169]

Some applications of C.D. measurements to problems in metal ion complexes, using nickel(II) and lanthanides as examples. L. I. Katzin, Coord. Chem. Rev., 1970, 5, 279-292 (12). [Pg.34]

Figure 2. Schematic of the SLM 8000 fluorometer. Excitation occurs through the excitation monochromator, and light emitted from the sample is observed in as many as four different positions. Photomultiplier tubes (PMTs) A, B, and C can be used to monitor fluorescence or right-angle light scatter through the monochromator (PMT A) or through filters (PUT B and C), and position D measures transmittance. Three channels can be monitored simultaneously with measurements being acquired at intervals of 1 s or less. The data are stored by the computer for subsequent manipulation. Figure 2. Schematic of the SLM 8000 fluorometer. Excitation occurs through the excitation monochromator, and light emitted from the sample is observed in as many as four different positions. Photomultiplier tubes (PMTs) A, B, and C can be used to monitor fluorescence or right-angle light scatter through the monochromator (PMT A) or through filters (PUT B and C), and position D measures transmittance. Three channels can be monitored simultaneously with measurements being acquired at intervals of 1 s or less. The data are stored by the computer for subsequent manipulation.
Table 11.14 gives critical stress, critical strain, and critical stored energy of NR-EPDM blends for initiation of ozone cracking. All the properties show an increase on addition of TOR, especially the critical stored energy. Stored energy is a strong indicator of ozone resistance and shows an increase by about 80% on addition of 20 parts of TOR to the compound. This was confirmed by SEM pictures of surface ozone cracks and the results of dynamic mechanical moduli and tan d measurement. [Pg.323]

A low accuracy of models for prediction of log D at any pH would not encourage the use of these models for practical applications in industry. Thus, it is likely that the methods for log D prediction at fixed pH that are developed in house by pharmaceutical companies will dominate in industry. However, log D measurements... [Pg.429]

Figure 8.9 Dynamics of STM-driven desorption and dissociation of chlorobenzene at Si(lll) (7 x 7) (a) before and (b) after a desorption scan the circles indicate the positions of chlorobenzene molecules before and after desorption (c) appearance of a chlorine adatom formed by dissociation of chlorobenzene with corresponding 3D image (d) measured rates of desorption and dissociation as a function of tunnelling current for a sample bias of + 3 V. (Reproduced from Ref. 26). Figure 8.9 Dynamics of STM-driven desorption and dissociation of chlorobenzene at Si(lll) (7 x 7) (a) before and (b) after a desorption scan the circles indicate the positions of chlorobenzene molecules before and after desorption (c) appearance of a chlorine adatom formed by dissociation of chlorobenzene with corresponding 3D image (d) measured rates of desorption and dissociation as a function of tunnelling current for a sample bias of + 3 V. (Reproduced from Ref. 26).
PCR is based on a PCA input data transformation that by definition is independent of the Y-data set. The approach to defining the X-Y relationship is therefore accomplished in two steps. The first is to perform PCA on the. Y-data, yielding a set of scores for each measurement vector. That is, if xk is the fcth vector of d measurements at a time k, then zk is the corresponding kth vector of scores. The score matrix Z is then regressed onto the Y data, generating the predictive model... [Pg.35]

Mountain, R.D. Thirumalai, D., Measures of effective ergodic convergence in liquids, J. Phys. Chem. 1989, 93, 6975-6979... [Pg.315]

Fig. 2.2. Log D measurement by liquid-liquid chromatography of compounds listed in Tab. 2.4. Note the scatter in measurement of compounds with low log D using Run type 1, caused because retention times are too short. These compounds are more reliably measured using Run type 2. Fig. 2.2. Log D measurement by liquid-liquid chromatography of compounds listed in Tab. 2.4. Note the scatter in measurement of compounds with low log D using Run type 1, caused because retention times are too short. These compounds are more reliably measured using Run type 2.
Schery, S.D., Measurements of Airborne Pb and uRn at Varied Indoor Locations Within the United States, Health Physics 49 1061-1067 (1985). [Pg.189]

The significance of biotests D, measured in the air or clean matrixes is used in the microplate photometers. [Pg.154]

Stern-Volmer Quenching Constants. d Measured in 15% methanol. Taken from refs. 15 and 18. e Measured in 2.5% DMSO. Taken from ref. 9. [Pg.228]

Stopping in front of another office, they flanked the doorway as if they d measured their distances from it equally on each side. Whatever the matter was, both were trying to be fair. I switched on the light and went in. [Pg.37]

Currie, L. A., Noakes, J., Breiter, D., Measurment of Small Radiocarbon Samples Power of Alternative Methods for Tracing Atmospheric Hydrocarbons, Ninth International Radiocarbon Conference, University of California, Los Angeles and San Diego, 1976. [Pg.186]

Let us examine some alternative results and consider the effects of the base fire dimension D. Measurements are given by Yokoi [3] for fire sources of Figure 10.9 and 20 cm radius (r0 = D/2). The temperature profiles... [Pg.313]

Gross, D., Measurement of flame length under ceilings, Fire Safety J., 1989, 15, 31—44. [Pg.334]


See other pages where D measurements is mentioned: [Pg.43]    [Pg.35]    [Pg.104]    [Pg.770]    [Pg.1381]    [Pg.529]    [Pg.353]    [Pg.85]    [Pg.98]    [Pg.100]    [Pg.419]    [Pg.72]    [Pg.169]    [Pg.390]    [Pg.16]    [Pg.30]    [Pg.41]    [Pg.434]    [Pg.88]    [Pg.62]    [Pg.230]    [Pg.232]    [Pg.387]    [Pg.397]    [Pg.15]    [Pg.220]   
See also in sourсe #XX -- [ Pg.428 ]




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