Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Ordering, measurement

Since we do not know the proper values for X and t, we need a way of Judging plausible values of X and t from the data. We do this by testing the transformed background measurements for normality. Our choice of a test for normality is the probability plot correlation coefficient r (12). The coefficient r is the correlation between the ordered measurements and predicted values for an ordered set of normal random observations. We denote the ordered background measure-ments by yB(l). where yB(l) < yB(2) < yBCnn) denote the... [Pg.123]

In the case when one of the two measurements of the contingency table is divided in ordered categories, one can construct a so-called thermometer plot. On this plot we represent the ordered measurement along the horizontal axis and the scores of the dominant latent vectors along the vertical axis. The solid line in Fig. 32.9 displays the prominent features of the first latent vector which, in the context of our illustration, is called the women/men factor. It clearly indicates a sustained progress of the share of women doctorates from 1966 onwards. The dashed line corresponds with the second latent vector which can be labelled as the chemistry/ other fields factor. This line shows initially a decline of the share of chemistry and a slow but steady recovery from 1973 onwards. The successive decline and rise are responsible for the horseshoe-like appearance of the pattern of points representing... [Pg.198]

What is behind the apparent disagreements between Tafel slopes and reaction orders reported from recent investigations of the ORR at PEFC cathode catalysts and the slopes and reaction orders measured earlier for model systems of low Pt surface area Is the ORR process at a dispersed Pt catalyst possibly different in nature from the ORR process at low-surface-area Pt ... [Pg.13]

In Pharmaceutical and Clinical Calculations, second edition, Drs. Mansoor Khan and Indra Reddy have provided a contemporary resource that can help pharmacy students learn the basic principles of how to accurately interpret prescriptions and medication orders, measure, calculate and compound quality dosage forms. In the latter chapters, the student can learn multiple methods to accurately and safely dose patients. The computational methods to accomplish these ends are clearly presented, and the examples used to demonstrate the concepts are relevant to contemporary practice. Pharmacy students will... [Pg.8]

For comparison, 2-parinaroyl-phosphatidylcholine (PPC) was also incorporated into the membrane preparations. For the Torpedo membranes, the acyl chain order measured by PPI was found to be lower than that by PPC, whereas the opposite was true for the vesicles. This inversion strongly suggests that PI has different interactions with certain membrane components compared to PC. In contrast, the correlation times of PPI and PPC were only slightly different in Torpedo membranes, and the values showed little difference with those measured in vesicles. [Pg.243]

However, if one applies the heterogeneous kinetics reported by Takagi et al. (1986), one can calculate that methyl nitrite concentrations of the order measured in the exhaust sample could arise by reactions of unburned methanol and N02 on the walls of the sampling bag prior to analysis (Finlayson-Pitts et al., 1992). [Pg.272]

Fig. 4.3.16. Tool steel C80 W3, Vickers indenter, load 294 mN, differential interference contrast, subnormal colour, grey of 1st order, measurement magnification 260 x, photograph enlargement 400 x. (After OPTON Feintechnik GmbH, Oberkochen)... Fig. 4.3.16. Tool steel C80 W3, Vickers indenter, load 294 mN, differential interference contrast, subnormal colour, grey of 1st order, measurement magnification 260 x, photograph enlargement 400 x. (After OPTON Feintechnik GmbH, Oberkochen)...
These examples illustrate how to obtain results about crystallinity and disorder for a better understanding of the relationships between structure and properties. The reader is, however, cautioned that crystallinity and disorder parameters determined by x-ray diffractometry are average values and that they should be carefully compared with local order measured by electron diffraction on ultra-thin cross sections of textile fibers (9) with differing crystallite sizes (10,11). [Pg.212]

In Ref. 31 it has been shown that long linear chains, as seen from the point of view of VB theory, show a long-range order, measured by the parameter p in Eq. (23), leading to a ground-state instability to bond alternation. From Sec. 5.3 also this is expected to occur. [Pg.756]

Results of Bulk Second-Order Measurements on Films and Composites... [Pg.323]

It is worth emphasizing that the reaction orders measured for the individual half-reactions are not necessarily the same as those for the overall corrosion reaction. Manipulation of Eqs. (7) and (8) to yield an expression for 7COrr predicts a reaction order (n0l) with respect to 02 (assuming [Cl-] constant) given by... [Pg.218]

The typical approach taken when attempting to vary the concentration of intermolecular modes is the use of binary mixtures. When one considers the many body nature of the intermolecular modes and the complexity of binary mixtures, it is not directly evident that there is any proportionality between the ill-defined concept of concentration for intermolecular modes and the binary mixture fraction. An additional complication in the use of binary mixtures comes from the significant changes in the polarizability weighted density of states as a function of binary mixture fraction. In other words, the intermolecular spectrum is changing with binary mixture fraction. These types of effects are clearly evident in third-order measurements of CS2 in binary mixtures (3). [Pg.480]

Rank annihilation factor analysis treats the special situation in which there are only two slices, where each slice contains the second-order measurements of one sample. One sample is usually a pure standard containing only the analyte of interest in a known concentration and the other is an unknown sample containing unknown interferents as well as the analyte of interest. The purpose in rank annihilation factor analysis is to estimate the concentration of the analyte of interest in the unknown sample. It is assumed that the signal from the analyte of interest corresponds to a rank-one component with the intensity proportional to the concentration. Thus the standard sample, say Xi, can be described... [Pg.137]

II. Ilf represents the F norm of a matrix, which is the square root of the sum of the squares of all elements. The matrix E is the error matrix of the second-order measurements. [Pg.315]

The maximum profit potential for a chemical reaction is only a crude, zeroth-order measure of value. To gain a better measure of the economics, we must have a fuller analysis of the process. The maximum profit potential can never be achieved because it costs money both to invest in the process hardware and to operate the process. If we simply were to try to maximize the potential profit by maximizing the conversion Xa, then we would need a reactor of infinite volume ... [Pg.404]

Since the isolated azide ion is centrosymmetric, it has a zero dipole moment. The quadrupole moment then gives the first-order measure of the ion s charge distribution. The parameters involved in a point-charge picture of the azide ion (the internitrogen distance d, and the charge q located on the terminal nitrogen atoms) are depicted in Figure 1. These parameters are related to Q33 by the equation... [Pg.198]

Sensitivity coefficients of second and higher order measure nonadditive effects. Consider the expression... [Pg.306]

Figure 5.2. Example of a zero-order measurement of combinatorial materials Abrasion resistance of coatings from measurements of scattered light from each organic coating in a 48-element array at a single wavelength upon abrasion test. (A) Reflected-light image of the coatings array (B) representative data from a single material in the array. Figure 5.2. Example of a zero-order measurement of combinatorial materials Abrasion resistance of coatings from measurements of scattered light from each organic coating in a 48-element array at a single wavelength upon abrasion test. (A) Reflected-light image of the coatings array (B) representative data from a single material in the array.
Figure S.3. Example of a first-order measurement of combinatorial materials. Polymer branching from measurements of fluorescence spectra from each polymerized material in a 96-element microreactor array at a single excitation wavelength. (A) Reflected-hght image of the microreactor array (B) representative fluorescence spectrum from a single microreactor in the array. Figure S.3. Example of a first-order measurement of combinatorial materials. Polymer branching from measurements of fluorescence spectra from each polymerized material in a 96-element microreactor array at a single excitation wavelength. (A) Reflected-hght image of the microreactor array (B) representative fluorescence spectrum from a single microreactor in the array.
Figure 5.4 Example of a second-order measurement of combinatorial materials. Sensor materials as a 48-element sensor materials array. (A) general view of the sensor materials array in a gas flow-through cell (B) representative absorption spectra from a single material in the array collected over a period of time of reaction of this sensor material with a vapor of interest. Figure 5.4 Example of a second-order measurement of combinatorial materials. Sensor materials as a 48-element sensor materials array. (A) general view of the sensor materials array in a gas flow-through cell (B) representative absorption spectra from a single material in the array collected over a period of time of reaction of this sensor material with a vapor of interest.
Figure 5.5. Example of a third-order measurement of combinatorial materials. Oxidative stability of polymers from measurements of UV-VIS reflection spectra from each polymeric composition in a materials array as a function of reaction temperature and time. (A) General view of the materials array on a gradient temperature heater (B) representative UV-VIS spectra from a single material in the array as a function of reaction time and temperature. Reaction temperatures Ti> T2> T. Reaction progress is shown as spectra changes from spectrum 1 to spectrum 7. Figure 5.5. Example of a third-order measurement of combinatorial materials. Oxidative stability of polymers from measurements of UV-VIS reflection spectra from each polymeric composition in a materials array as a function of reaction temperature and time. (A) General view of the materials array on a gradient temperature heater (B) representative UV-VIS spectra from a single material in the array as a function of reaction time and temperature. Reaction temperatures Ti> T2> T. Reaction progress is shown as spectra changes from spectrum 1 to spectrum 7.

See other pages where Ordering, measurement is mentioned: [Pg.123]    [Pg.12]    [Pg.108]    [Pg.117]    [Pg.349]    [Pg.368]    [Pg.385]    [Pg.373]    [Pg.279]    [Pg.745]    [Pg.291]    [Pg.291]    [Pg.315]    [Pg.321]    [Pg.324]    [Pg.45]    [Pg.101]    [Pg.12]    [Pg.123]    [Pg.9]    [Pg.168]    [Pg.267]    [Pg.31]    [Pg.545]    [Pg.96]   
See also in sourсe #XX -- [ Pg.472 ]




SEARCH



Absorbance, Order Parameter, and Dichroic Ratio Measurement

B Response of a Second-Order Temperature Measuring Element

Conformational Studies Using Second-Order NLO Activity Measurements

Control measures order

Coupling constant measuring first-order spectra

First-order measurement

First-order reactions derivative measurement

Homogeneous kinetic measurements first-order following reaction

Measurement of third-order nonlinear

Measurements of Molecular Orientations from Ordered Samples

Measuring coupling constants from first-order spectra

Measuring coupling constants second order spectra

Molecular second-order measurements

Molecular second-order measurements complexes

Neutron diffraction measurements ordering

Order parameters measurement

Order splits, measuring

Second-order measurement

Second-order measuring element

Second-order nonlinear optical measurement

Second-order nonlinear optical measurement techniques

Second-order nonlinear optics measurement

Similarity measure and order parameter

Structural order parameters crystal-independent measures

Third-Order Measurements

Third-order nonlinear optical effects measurement

Third-order nonlinear optical measurement

Third-order nonlinear optical measurement degenerate four-wave mixing

Third-order nonlinear optical measurement techniques

Third-order nonlinear susceptibilities measurement

© 2024 chempedia.info