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Campbell solutions

For consistency, structures are drawn as the isoquinoline-1,4-diol throughout regardless of tautomer drawn in the original reference. The actual tautomeric structure is dependent on the pH of the solution. See Caswell, L. R. Campbell, R. D. J. Org. Chem. 1961, 26,4175. [Pg.422]

The analytic theory outlined above provides valuable insight into the factors that determine the efficiency of OI.EDs. However, there is no completely analytical solution that includes diffusive transport of carriers, field-dependent mobilities, and specific injection mechanisms. Therefore, numerical simulations have been undertaken in order to provide quantitative solutions to the general case of the bipolar current problem for typical parameters of OLED materials [144—1481. Emphasis was given to the influence of charge injection and transport on OLED performance. 1. Campbell et at. [I47 found that, for Richardson-Dushman thermionic emission from a barrier height lower than 0.4 eV, the contact is able to supply... [Pg.545]

Siekierska, Sokolowska and Campbell irradiated ASCI3 in benzene solution in order to test the efficacy of billiard-ball mechanisms in... [Pg.69]

Blood Dilution of sample with ammonium solution containing Triton X-100 ICP/MS 15 pg/L 96-111 Delves and Campbell 1988... [Pg.445]

This equation must be solved for yn +l. The Newton-Raphson method can be used, and if convergence is not achieved within a few iterations, the time step can be reduced and the step repeated. In actuality, the higher-order backward-difference Gear methods are used in DASSL [Ascher, U. M., and L. R. Petzold, Computer Methods for Ordinary Differential Equations and Differential-Algebraic Equations, SIAM, Philadelphia (1998) and Brenan, K. E., S. L. Campbell, and L. R. Petzold, Numerical Solution of Initial-Value Problems in Differential-Algebraic Equations, North Holland Elsevier (1989)]. [Pg.50]

Campbell, I. Cupertino, D. C. Emeleus, L. C. Harris, S. G. Owens, S. Parsons, S. Swart, R. M. Tasker, P. A. Tinkler, O. S. White, D. J. Diazopyrazolones as solvent extractants for copper from ammonia leach solutions. International Solvent Extraction Conference, Cape Town, South Africa, Mar. 17-21, 2002, 347-352. [Pg.802]

It applies for both formulations above that the expansion in principle contains an infinite number of terms. The convergence to a few lowest order terms relies on the ability to orderly separate influences of the dominant rf irradiation terms (through a suitable interaction frame) from the less dominant internal terms of the Hamiltonian. In principle, this may be overcome using the spectral theorem (or the Caley-Hamilton theorem [57]) providing a closed (i.e., exact) solution to the Baker-Campbell-Hausdorf problem with all dependencies included in n terms where n designates the dimension of the Hilbert-space matrix representation (e.g., 2 for a single spin-1/2, 4 for a two-spin-1/2 system) [58, 59]. [Pg.9]

Campbell, P. G. C., Twiss, M. R. and Wilkinson, K. J. (1997). Accumulation of natural organic matter on the surfaces of living cells implications for the interaction of toxic solutes with aquatic biota, Can. J. Fish. Aquat. Sci., 54, 2543-2554. [Pg.267]

Unsubstituted cycloamyloses have been used to catalyze a number of reactions in addition to acyl group transfer. Brass and Bender (8) showed that cycloamyloses promoted phenol release from diphenyl and bis(p-nitro-phenyl) carbonates and from diphenyl and bis(m-nitrophenyl)methyl phos-phonates. Breslow and Campbell (10,11) showed that the reaction of anisole with HOCL in aqueous solution is catalyzed by cyclohexaamylose and cycloheptaamylose. Anisole is bound by the cyclodextrins and is chlorinated exclusively in the para position while bound. Cycloheptaamylose has been used to promote regiospecific alkylation followed by the highly selective oxidation shown in reaction (3) (95). In addition cycloheptaamylose effec-... [Pg.202]

Campbell has studied the separation of technetium by extraction with tributyl phosphate from a mixture of fission products cooled for 200 days. Nearly complete separation of pertechnetate is achieved by extraction from 2 N sulfuric acid using a 45 % solution of tributyl phosphate in kerosene. Ruthenium interferes with the separation and is difficult to remove without loss of technetium other radioisotopes can be removed by a cation-exchange process. However, this separation procedure has not been widely applied because of the adverse influence of nitrate. [Pg.116]

Campbell, J.R., Luthy, R.G., and Carrondo, M.J.T. Measurement and prediction of distribution coefficients for wastewater aromatic solutes, Environ. Sci. Technol., 17(10) 582-590, 1983. [Pg.25]

Dermal/Ocular Effects. Corrosive damage to the skin has been reported in humans dermally exposed to cresols (Cason 1959 Green 1975 Herwick and Treweek 1933 Klinger and Norton 1945 Pegg and Campbell 1985). In one patient, disfiguring scars remained visible 1 year after exposure (Herwick and Treweek 1933). However, no reaction to cresol was noted when it was applied to the skin as a 1% solution in alcohol (Reimann 1933). [Pg.48]

Figure 1.13. Crystal structure of solution-grown pentacene along (a) the c-axis and (b) the fe-axis. Pl,a = 0.790 nm, b = 0.606 nm, c = 1.601 nm, a = 101.9°, P = 112.6°, y = 85.8°. Crystallographic data from Campbell et al, 1961. See Table 1.10 for comments on the values of the lattice parameters. Crystal structure of p-6P (c) c-planes along their long molecular axis and (d) along the fe-axis. P2i /c, a = 2.624 nm, b = 0.557 nm, c = 0.809 nm, p = 98.17°. Crystallographic data from Baker et al, 1993. Crystal stmcture of o -6T (e) fee-plane and (f) projection along the c-axis. P2ifn,a = 4.471 nm,fe = 0.785 nm,c = 0.603 nm,jS = 90.76°. Crystallographic data from Horowitz et al, 1995. Figure 1.13. Crystal structure of solution-grown pentacene along (a) the c-axis and (b) the fe-axis. Pl,a = 0.790 nm, b = 0.606 nm, c = 1.601 nm, a = 101.9°, P = 112.6°, y = 85.8°. Crystallographic data from Campbell et al, 1961. See Table 1.10 for comments on the values of the lattice parameters. Crystal structure of p-6P (c) c-planes along their long molecular axis and (d) along the fe-axis. P2i /c, a = 2.624 nm, b = 0.557 nm, c = 0.809 nm, p = 98.17°. Crystallographic data from Baker et al, 1993. Crystal stmcture of o -6T (e) fee-plane and (f) projection along the c-axis. P2ifn,a = 4.471 nm,fe = 0.785 nm,c = 0.603 nm,jS = 90.76°. Crystallographic data from Horowitz et al, 1995.
The automotive engineers were also busy. In 1931 Lovell, Campbell, and Boyd (23) published data on an extended series of pure paraffin and olefin hydrocarbons in fairly dilute solution in gasoline. These data showed a number of definite relations between the molecular structure of the pure hydrocarbon and the tendency of the fuel to knock. The... [Pg.356]

Szardenings, A. K. Burkoth, T. S. Look, G. C. Campbell, D. A. A Reductive Alkylation Procedure Applicable to Both Solution- and Solid-Phase Syntheses of Secondary Amines, J. Org. Chem. 1996, 61, 6720. [Pg.113]

Look, G. C. Murphy, M. M. Campbell, D. A. Gallop, M. A. Trimethylor-thoformate A Mild and Effective Dehydrating Reagent for Solution and Solid-Phase Imine Formation, Tetrahedron Lett. 1995, 36, 2937. [Pg.113]

The heat of transition from form III to form II is 310 keal/mol and that from form II to form I is 979 kcal/mol. Whetstone (Ref 113) studied the initiation of transition between forms III and IV. The effect of foreign substances on the transition IV III was studied by Campbell and Campbell (Ref 81) who found that in the case of a solid solution of 8. to 10% of KNOj in AN the temperature of transition of form III into form IV is depressed by about 20°. Such solid solutions can be prepared either by fusion or by co-crystallization from aqueous solutions. Hendricks et al (Ref 40) found form III to be ortho rhombic and form V to exist up to -18° and not to -16°. Bowen (Ref 30) showed that there is also a metastable inversion occurring at about 50° as follows orthorhombic form (j3)(32. l°to -16°) tetragonal form (5)(125-2° to 84.2°). [Pg.311]

K.E. Brenan, S.L. Campbell, and L.R. Petzold. Numerical Solution of Initial-Value Problems in Differential Algebraic Equations. SIAM, Philadelphia, PA, second edition, 1996. [Pg.816]

Tn 1842 Biot (I) observed that the addition of certain sugars increased A the acidity of boric acid solutions. Research during the next one hundred years revealed that this phenomenon results from the formation of sugar-boric acid esters which were stronger acids than boric acid and that there are certain configurational requirements which sugars must satisfy to react with boric acid. Reviews of the research done during this period have been presented by Roy et al. (2), Boeseken (3), Weser (4), and Nies and Campbell (5). [Pg.216]

The diversity of protein structures has already been mentioned. It is a property of proteins to bind other molecules—water, ions, neutral solutes such as sugars, lipid soluble molecules, other proteins and nucleic acids. Binding sites may be on the surface of the molecule, in a crevice or, with membrane bound proteins, projecting into the extracellular fluid or cytoplasm. Over time, many binding sites have become highly specific, with binding constants > 106 or indeed > 109. The structure of many such sites are now known (Campbell, 1996). [Pg.273]

Downing, A. K, Knott, V., Werner, J. M., Cardy, C. M., Campbell, I. D., and Handford, P. A. (1996). Solution structure of a pair of calcium-binding epidermal growth factor-like domains Implications for the Marfan syndrome and other genetic disorders. Cell 85, 597-605. [Pg.430]


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