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Sample property

If the target analyte is ionizable, the pK of the analyte should be determined or obtained. Software packages such as ACD (Advanced Chemistry [Pg.361]

Development), Pallas (CompuDrug Chemistry Ltd, Budapest, Hungary), and so on, may be used to get an estimated pKa value for the ionizable functionalities on the molecule. In Section 8.7, discussion on analyte p/C from an analytical chemist s perspective is given. [Pg.362]

discussions with the early-phase drug discovery and/or preformulation groups may provide this information because they may have already ascertained the pA of the molecules by titration or other experimental methods (nlON, etc). Table 8-3 shows some of the more common ionizable functionalities present in pharmaceutical compounds. [Pg.362]

2 Solubility of Components and Diluent Effects (Matrix Effects). Solubility of the analyte is also very important. Solubility of a particular durg [Pg.362]

There are also other scenarios that should be considered for peak distortion of early eluting components. [Pg.365]


Other recent investigations involving AES, often with depth profiling, deal with the surface segregation of Ag in Al-4.2 % Ag [2.163], of Sn in Cu and formation of superficial Sn-Cu alloy [2.164], of Mg in Al-Mg alloy [2.165], and of Sb in Ee-4% Sb alloy [2.166]. Note the need to differentiate between, particularly, segregation, i. e. original sample properties, from the artifact of preferential sputtering. [Pg.47]

In general, luminescence measurements are relative rather than absolute, since the Instrument characteristics and sample properties that determine the fluorescence Intensities are often not well defined. Absolute luminescence measurements are difficult to perform and require time and Instrumentation not available In most laboratories. Thus, luminescence measurements rely heavily on standards to determine Instrument responses and parameters, the chemical composition of samples, and the characteristics of chemical systems. To... [Pg.98]

Havel, T. F. The sampling properties of some distance geometry algorithms applied to unconstrained polypeptide-chains a smdy of 1830 independently computed conformations. Biopolymers 1990, 29,1565-1585. [Pg.252]

Porter PS, Rao ST, Ku J-Y, Poirot RL, Dakins M (1997) Small sample properties of nonparametric bootstrap t confidence intervals. J Air Waste Management Assoc 47 1197-1203 Powell R, Hergt J, Woodhead J (2002) Improving isochron calcttlatiorrs with robust statistics and the bootstrap. Chem Geol 185 191- 204... [Pg.652]

Repeated measurements of the same measurand on a series of identical measuring samples result in random variations (random errors), even under carefully controlled constant experimental conditions. These should include the same operator, same apparatus, same laboratory, and short interval of the time between measurements. Conditions such as these are called repeatability conditions (Prichard et al. [2001]). The random variations are caused by measurement-related technical facts (e.g., noise of radiation and voltage sources), sample properties (e.g., inhomogeneities), as well as chemical or physical procedure-specific effects. [Pg.95]

Experimental Materials. All the data to be presented for these illustrations was obtained from a series of polyurethane foam samples. It is not relevant for this presentation to go into too much detail regarding the exact nature of the samples. It is merely sufficient to state they were from six different formulations, prepared and physically tested for us at an industrial laboratory. After which, our laboratory compiled extensive morphological datu on these materials. The major variable in the composition of this series of foam saaqples is the aaK>unt of water added to the stoichiometric mixture. The reaction of the isocyanate with water is critical in determining the final physical properties of the bulk sample) properties that correlate with the characteristic cellular morphology. The concentration of the tin catalyst was an additional variable in the formulation, the effect of which was to influence the polymerization reaction rate. Representative data from portions of this study will illustrate our experiences of incorporating a computer with the operation of the optical microscope. [Pg.158]

Different factors contribute to the mechanical properties of plant tissue cell turgor, which is one of the most important ones, cell bonding force through middle lamella, cell wall resistance to compression or tensile forces, density of cell packaging, which defines the free spaces with gas or liquid, and some factors, also common to other products, such as sample size and shape, temperature, and strain rate (Vincent, 1994). Depending on the sample properties (mainly turgor and resistance of middle lamella), two failure modes have been described (Pitt, 1992) cell debonding and cell rupture. [Pg.205]

The least-square solution itself does not depend on the probability distribution of y it is simply a minimum-distance estimate. Later in this Chapter, it will be shown, however, that its sampling properties are most easily described when the measurements are normally distributed. [Pg.250]

We will now investigate the sampling properties of the statistic representing the weighted sum of squared residuals i1 given by equation (5.4.13). We first observe that the slightly different expression (y — l)rSy i(y —is zero since... [Pg.291]

Where C is a matrix of component concentrations or sample properties, S is a matrix of basis vectors (pure component spectra, or spectral profiles reflecting a pure sample property), and E and Ec are model residuals. The direct model expresses the analyzer responses (X) as a function of concentrations, whereas the inverse model expresses concentrations as a function of the analyzer responses. Because the former is more in line with the Beer-Lambert Law (absorbance = concentration x absorptivity), it is given the label direct . [Pg.377]

Stein M. 1987. Large sample properties of simulations using Latin hypercube sampling. Technometrics 29 143-151. [Pg.68]

The properties of a pulse have to be evaluated by applying the pulse directly to the spin system under study in order to account for parameters such as multiplet width, relaxation, sample properties, and setup and behavior of the spectrometer. This practical approach can be supported by numerical simulations, especially for complicated shapes. [Pg.15]

Sampling Location Sampling Property Type of Sample Sample Quantity Sampling Time Surface Area in Contact with Product Solution Final Volume of Rinse ... [Pg.1054]


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See also in sourсe #XX -- [ Pg.44 , Pg.447 ]

See also in sourсe #XX -- [ Pg.24 ]




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Experimental Investigation of the Properties Absent in Bulk Samples

Finite-Sample Properties of the Least Squares Estimator

Heterogeneous Samples Viscosity and Surface Properties

Measurement of sample properties without unwanted annealing effects

Mechanical properties of samples

Method development sample properties consideration

Optical properties, spectroscopy irradiated samples

PROPERTIES OF THE FSF MODEL WITH FAST SAMPLING

Physicochemical properties of the sample

Properties of sediments outcrop samples

Properties of the sample

Rock sample, properties

Sample Properties of the Least Squares and Instrumental Variables Estimators

Sample Specifications by Examples and Properties

Sample optical properties

Sample physicochemical properties

Samples, fatigue properties

Sampling properties

Sampling properties

Structure and Properties of the Crystallized Samples

True Nanoferroics with the Properties Absent in Corresponding Bulk Samples

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