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Species matrix

Asymmetric diarylmethanes, hydrogenolytic behaviors, 29 229-270, 247-252 catalytic hydrogenolysis, 29 243-258 kinetics and scheme, 29 252-258 M0O3-AI2O3 catalyst, 29 259-269 relative reactivity, 29 255-257 schematic model, 29 254 Asymmetric hydrogenations, 42 490-491 Asymmetric synthesis, 25 82, 83 examples of, 25 82 Asymmetry factor, 42 123-124 Atom-by-species matrix, 32 302-303, 318-319 Atomic absorption, 27 317 Atomic catalytic activities of sites, 34 183 Atomic displacements, induced by adsorption, 21 212, 213 Atomic rate or reaction definition, 36 72-73 structure sensitivity and, 36 86-87 Atomic species, see also specific elements adsorbed... [Pg.51]

Fig. 10.14. MALDI spectra of protein extracts from Bacillus species (matrix a-CHCA). (a) B. anthracis (Sterne), (b) B. thuringiensis (4A1), (c) B. cereus (6E1), (d) B. sub-... Fig. 10.14. MALDI spectra of protein extracts from Bacillus species (matrix a-CHCA). (a) B. anthracis (Sterne), (b) B. thuringiensis (4A1), (c) B. cereus (6E1), (d) B. sub-...
Examination of the matrix given in Table XV brings up an item of special interest. If the combination s4 of atomic oxygen were assumed not to occur, we would still be able to produce ethylene oxide by a combination of the first three steps. This scheme could place a lower limit on the selectivity at 6 7 or 85.7%, corresponding to a simple overall reaction rather than a multiple overall reaction. This serves to illustrate that we get fewer overall reactions than would be predicted by considering only the atom-by-species matrix, as a result of a more restricted choice of possible steps. [Pg.302]

We will use this name for the species matrix, rather than the pisp in BasicBiochemData3 to avoid shadowing. [Pg.73]

Module[, ( estersp is the species matrix of the ester, sugar is the species matrix of the sugar. is in kJ mol. )... [Pg.236]

The output is the species matrix without the standard enthalpies of formation of the three species. )... [Pg.443]

ArH ° (298.15 K) to calculate the standard enthalpy of formation (1=0) of the two species of a reactant for which the species matrix (spmat) contains AfG° at zero ionic strength for the two species of the reactant. The reaction equation (equat) is of the form mannoseh+pih-x-h2oh= 1.7, where 1.7 kJ mol -1 is the heat of reaction and x is mannnoseSphosh. The species matrix (spmat) is that for mannoseSphos. The calorimetric experiment is at pH and ionic strength ionstr. The first step in the calculation is to use the information on the standard Gibbs energies of formation of the species of the reactant of interest to calculate the equilibrium mole fractions rl (base form) and r2 (acidform) of the two species of the reactant of interest. The final output is the complete species matrix for x. )... [Pg.444]

Metadata are most easily provided in pick lists that appear as dropdown menns in the nser interface. New files in the system wonld typically receive mnltiple metadata. To stay with the previous example, each new metabolite would receive metadata for Species, Matrix, Tissue, and so forth. There are certain cases in which previously selected metadata (primary metadata) may affect the number of entries in a pick list of other metadata (secondary metadata). Selecting the primary metadata would then lead to exclusion of several nonapplicable secondary metadata or exclusion of an entire meta-key. [Pg.318]

Nonspecific nonspecificity results from interference of matrix components that are structurally unrelated to the analyte of interest. Examples of such interfering matrix components would include serum proteins, lipids, heterophilic antibodies, rheumatoid factor, proteases, and so on. Nonspecific nonspecificity is often referred to as matrix effect. Figure 4.3 depicts the impact of matrix on the assay performance. Matrix interference is one of the chief reasons that LB As often require more method development and validation prior to switching from one species matrix to another or even within the same species. In addition, we recommend during clinical study support that matrix from the relevant disease populations be tested for matrix effects as soon as that matrix becomes available. Matrix effects should be evaluated by comparing the concentration response relationship of both spiked and unspiked samples of the biological matrix (recommendation is 10 or more lots of individual sources) to a comparable buffer solution. It is recommended that the spiked sample... [Pg.89]

Sometimes balancing is carried out without the formulation of reaction equations. This situation, however, arises rarely when kinetics are of interest. In this case an element-species matrix can be written on the basis of N species (components) with k elementary balances... [Pg.407]

The element-species matrix that represents the elemental composition of the flows of compounds can be written in this case as... [Pg.408]


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See also in sourсe #XX -- [ Pg.133 ]




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Atom-by-species matrix

Chromium species matrix studies

Element-species matrix

High species, matrix isolation

Matrices glassy, excited species

Matrix-isolated species, isotopic substitution

Photochemistry and Matrix-isolated Species

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