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Minor product matrix

Q-mode factor analysis is based on a major product matrix, XX. Whereas the R-mode analyses focus on interrelationships among variables, Q-mode analyses focus on interrelationships among objects. Accordingly, the major product matrix is usually a distance or similarity matrix. Formally, Q-mode and R-mode factor analyses are closely related because the nonzero eigenvalues of the major product matrix are identical to the eigenvalues of the minor product matrix, and the eigenvectors are easily derived from one another (28). [Pg.69]

Besides MeAPO, several heterogeneous systems have been proposed for the oxidation of cydohexane vith various oxidants [2c], but almost all of them yield 01/ One as the main reaction products, with AA being only a minor product. Heterogeneous catalysts can be either oxides or metal cations and complexes incorporated on inorganic matrixes, such as active carbon, zeolites, aluminophosphates or conventional supports such as alumina and silica. The activity of these systems is greatly affected by the choice of solvent, which determines the polarity of the medium. In addition, the hydrophobicity of the support is important, since a hydrophobic environment rapidly expels the oxidized products from the reaction zone. When oxygen is used as the oxidant, these systems often need small amounts of hydroperoxides as co-catalysts. [Pg.394]

ESR work (16) shows that 2-pentyl radicals (CH3—CH2—CH2— CH—CH3) are trapped in solid n-pentane irradiated at 77 °K. Careful examination of the ESR signal indicates that other radicals are produced with much lower yields than 2-pentyl radicals. The measurements do not allow the identification of these minor products. When the temperature of the sample is raised, the ESR signal disappears just below the melting point of the n-pentane matrix. [Pg.306]

The matrix photochemistry of the 2,3-dimethylbut-2-ene complex with N2O4 (the NOj dimer) has also been investigated. " In this case the major product was 2,3-dimethyl-3-nitroso but-2-yl nitrate, a nitroso nitrate, and the minor product 2,3-dimethyl-3-nitrobut-2-yl nitrite, a nitro nitrite. The mechanism by which the observed products were formed appeared to be distinct from that previously suggested for the thermal reaction of alkenes with N2O4 in solution. [Pg.241]

An intriguing alternative entry into this type of cyclohexadienylidene chemistry has been provided by matrix isolation studies of the photolysis of a-diazo-2-ethynylacetophenone (46) (Scheme 8). Irradiation of 46 at 403 nm in solid argon gave the ketene 48 as the major product but also the carbene 50 as a minor product. Carbene 50 was reversibly converted into 49 on irradiation at A > 475 nm. Thus, the Wolff rearrangement of ketocarbene 47, which was not observed directly, competed with the intramolecular addition of the carbene center to the triple bond. [Pg.297]

Gierczak et al. (1997) observed methane, ethylene, acetylene, allene, and propyne as major products formaldehyde, methanol, formic acid, acetic acid, and hydrox-yacetone were identihed as minor products. The mechanism of formation of these products is unclear. Two expected products, observed by Raber and Moortgat (1996), propene and dimethylketene, were not observed, and CO and CO2 products observed by Raber and Moortgat, were not measured by Gierczak et al. (1997). In argon matrix-isolated studies of methacrolein photochemistry (4.2 K) and with A, >300 nm, Johnstone and Sodeau (1992) observed the isomerization of the original trans-methacrolein to di-methacrolein no HCO, CO, or propene could be detected. In similar matrix experiments at A >230 nm, dimethylketene, CO, and propene were observed together with other unidentified products. [Pg.1036]

Wavelength dispersive x-ray fluorescence spectrometric (xrf) methods using the titanium line at 0.2570 nm may be employed for the determination of significant levels of titanium only by carefiil matrix-matching. However, xrf methods can also be used for semiquantitative determination of titanium in a variety of products, eg, plastics. Xrf is also widely used for the determination of minor components, such as those present in the surface coating, in titanium dioxide pigments. [Pg.134]

There are numerous methods in the literature for the determination of caffeine, theobromine, and theophylline in food matrices, including coffee, tea, and cocoa. Until recently, methods have emphasized the determination of the major methylxanthines in a commodity, for example, caffeine in coffee or theobromine in cocoa. Present methods range from being specific for one of the compounds in a single matrix to being an all-encompassing assay of major and minor methylxanthines in food products. [Pg.27]

If the photo-Fries reaction would occur via a concerted mechanism, the absence of solvent should be of minor importance for the formation of rearranged products. However, conclusive evidence supporting the radical pair mechanism arises from the experiments carried out with phenyl acetate (10) in the vapor phase. The major product in the irradiations of 10 is phenol (13), which accounts for 65% of the photoproducts. Under these conditions, less than 1% of ortho -hydroxyace-tophenone (11) appears to be formed [19,20]. Conversely, when a high cage effect is expected, as in rigid matrixes (i.e., polyethylene), the result is completely different, and phenol is practically absent from the reaction mixtures [29]. In the intermediate situation (liquid solution), both rearranged products and phenol are formed in variable amounts depending on solvent properties. These observations... [Pg.49]

Additives are used for a variety of purposes to improve processing, to modify performance or appearance, to prevent or retard aging, to reduce cost. They are normally incorporated into the polymer matrix during compounding and may constitute a major or minor part of the final product. For this reason it is not always useful to define additives in terms of the amount of that ingredient present. Additives may, or may not, interact chemically with the... [Pg.393]

Soybeans and soybean products contain high levels of protein, carbohydrates, and lipids (Table 11.6.1). As minor components of complex mixtures, isoflavones must first be separated from the bulk of the matrix constituents prior to analysis. Efficient extraction methods for isoflavones should account for their diverse structures, chemical properties, and the food matrix of which they are constituents. This unit describes a practical way of extracting isoflavones from soybean products in their natural forms using readily available solvents and laboratory equipment. [Pg.1298]

Photolysis of 6 in a formaldehyde-doped argon matrix (0.6%) yielded also silene 7 as the major product but also minor quantities of other products. Warming of the matrix to 30-35 K allowed the direct spectroscopic observation of the reaction between 7 and formaldehyde. The intensity of the IR absorptions of these compounds disappeared to a large extent, and in addition to 8 a new product, which could be identified... [Pg.1146]

The observed product distributions reflect the influence of both factors. In the parent compound 102 and in the silyl substituted 104, the initially formed open-chain silylenes 103 and 146 are relatively sensitive and the migration tendency of the group R is quite large, and therefore the silacyclopropenylidenes 104 and 145 are found. In contrast, the methyl and the ethynyl compound 138 and 150 are stable enough to pass the pyrolysis tube and both can be matrix-isolated upon pyrolysis of the appropriate precursors 137 and 149. Due to the small migration tendencies of the methyl and the ethynyl group, the rearrangement product 135 is not found at all and 151 is detected only in relatively minor amounts. [Pg.1174]

A minor for element ay of matrix A is the determinant for the matrix obtained from matrix A with the ith row and jth column omitted. An algebraic complement for element atj of matrix A is its minor multiplied by (— l)i+J. Matrix determinant amounts to the sum of the products of elements for some column (or row) with their algebraic complements. [Pg.12]


See other pages where Minor product matrix is mentioned: [Pg.68]    [Pg.68]    [Pg.174]    [Pg.400]    [Pg.433]    [Pg.497]    [Pg.1353]    [Pg.275]    [Pg.269]    [Pg.64]    [Pg.120]    [Pg.1352]    [Pg.69]    [Pg.433]    [Pg.184]    [Pg.202]    [Pg.20]    [Pg.452]    [Pg.282]    [Pg.48]    [Pg.14]    [Pg.12]    [Pg.452]    [Pg.777]    [Pg.116]    [Pg.107]    [Pg.236]    [Pg.59]    [Pg.431]    [Pg.204]    [Pg.19]    [Pg.289]    [Pg.318]    [Pg.693]    [Pg.1021]    [Pg.385]    [Pg.92]   


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Matrices minors

Minor product

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