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H-transformation

Uniform mixing in the vertical to 1000 m and uniform concentrations across each puff as it expands with the square root of travel time are assumed. A 0.01 h transformation rate from SO2 to sulfate and 0.029 and 0.007 h" dry deposition rates for SO2 and sulfate, respectively, are used. Wet deposition is dependent on the rainfall rate determined from the surface obser% ation network every 6 h, with the rate assumed to be uniform over each 6-h period. Concentrations for each cell are determined by averaging the concentrations of each time step for the cell, and deposition is determined by totaling all depositions over the period. [Pg.332]

Fig. 2. Depiction of conformal mapping of graphene lattice to [4,3] nanotube. B denotes [4,3] lattice vector that transforms to circumference of nanotube, and H transforms into the helical operator yielding the minimum unit cell size under helical symmetry. The numerals indicate the ordering of the helical steps necessary to obtain one-dimensional translation periodicity. Fig. 2. Depiction of conformal mapping of graphene lattice to [4,3] nanotube. B denotes [4,3] lattice vector that transforms to circumference of nanotube, and H transforms into the helical operator yielding the minimum unit cell size under helical symmetry. The numerals indicate the ordering of the helical steps necessary to obtain one-dimensional translation periodicity.
Fig. 3. Schematic illustration of the growth process of a graphitic particle (a)-(d) polyhedral particle formed on the electric arc (d)-(h) transformation of a polyhedral particle into a quasi-spherical onion-like particle under the effect of high-energy electron irradiation in (f) the particle collapses and eliminates the inner empty space[25j. In both schemes, the formation of graphite layers begins at the surface and progresses towards the center. Fig. 3. Schematic illustration of the growth process of a graphitic particle (a)-(d) polyhedral particle formed on the electric arc (d)-(h) transformation of a polyhedral particle into a quasi-spherical onion-like particle under the effect of high-energy electron irradiation in (f) the particle collapses and eliminates the inner empty space[25j. In both schemes, the formation of graphite layers begins at the surface and progresses towards the center.
JA5190). Upon deprotonation by bases, 285 (R = H) transforms to 286, and 285 (R = Me) goes to 287 because the C2 position is occupied. Protonation of 286 with triflic acid occurs at position 3 of the heteroring to form the benzothienyl carbene complex 288, and deprotonation reverts it to 286. This kind of process is a rarity for the uncomplexed benzothiophenes (81AHC171). [Pg.44]

The sonochemically produced anatase subjected to heat treatments under ambient atmospheric conditions and at temperatures from 773 to 1,073 K and times between 1-72 h transformed only to rutile. [Pg.201]

As these charge-change rates may be important in nonequilibrium situations, it is worthwhile to examine them more closely. Consider, for definiteness, the case i = 0, j = +. We define the rate constant r0+ to be the rate at which a given H° transforms into H+ it consists of the two terms just mentioned, so that... [Pg.257]

Catalytic exchange of hydrocarbons, 11 223 Catalytic heterogeneous reactions, 37 134-151 Arrhenius expression, 37 134, 136 C H, transformation on transition-metal surfaces, 37 141-147... [Pg.68]

Dyker G (2005) Handbook of C-H transformations applications in organic synthesis. Wiley, Weinheim, Germany... [Pg.46]

H Transforming the metal-containing compound to a metal is less energy intensive... [Pg.622]

Figure 5. Three-component composition simplex with path grid, and its h-transform. (For an = 2 and a13 = 4)... Figure 5. Three-component composition simplex with path grid, and its h-transform. (For an = 2 and a13 = 4)...
Fig. 2.59. Tracing out the carbon skeleton of C10H20O by a two-dimensional INADEQUATE experiment in combination with two DEPT experiments (100.6 MHz (a b) 400 mg in 1 mL, (c-e) 50 mg in 0.4 mL of deuteriochloroform at 30CC measuring time for (a) 14 h transform time 50 min) (a) contour plot of the INADEQUATE matrix (b) subspectra of all 13C — 13C bonds u k (c) proton-decoupled 13C NMR spectrum (d -e) DEPT experiments for generation of a CH carbon subspectrum (d) and for separation of CH2 carbon atoms (negative) from CH and CH3 groups (positive). Fig. 2.59. Tracing out the carbon skeleton of C10H20O by a two-dimensional INADEQUATE experiment in combination with two DEPT experiments (100.6 MHz (a b) 400 mg in 1 mL, (c-e) 50 mg in 0.4 mL of deuteriochloroform at 30CC measuring time for (a) 14 h transform time 50 min) (a) contour plot of the INADEQUATE matrix (b) subspectra of all 13C — 13C bonds u k (c) proton-decoupled 13C NMR spectrum (d -e) DEPT experiments for generation of a CH carbon subspectrum (d) and for separation of CH2 carbon atoms (negative) from CH and CH3 groups (positive).
The reagent system TMS-azide/triflic acid performs efficient animation57 of arenes, while the combination of TMS-azide and A-bromosuccinimide with Nafion-H transforms alkenes into /J-bromoalkyl azides58. On the other hand, the combination of TMS-azide and chromium trioxide converts alkenes into a-azidoketones59 and aldehydes into acyl azides60. [Pg.1674]

Biotransformation k 3 10 9to3 x 10 GuLcell h. transformation for bacteria in water (Mabey ctal. 1982) Bioconcentration, Uptake (kj) and Elimination (k2) Rate Constants ... [Pg.1117]

Coll, J. C., Tapiolas, B. F., Bowden, B. F., Webb, L., and Marsh, H., Transformation of soft coral (Coelenterata Octocorallia) terpenes by Ovula ovum (Mollusca Prosobranchia), Mar. Biol, 74, 35, 1983. [Pg.147]

The general aim of C-H transformation is to introduce groups with a higher complexity to hydrocarbon structures. Industrial processes therefore usually involve transformation of C-H groups starting from simple molecules. The reactions employed are selective oxidation, substitution (radical, electrophilic), nitration, ammoxidation, and sulfonation. The functionalized molecules are then further converted to more valuable products and intermediates by different reaction pathways. The latter often comprise further steps of C-H-activation. [Pg.14]


See other pages where H-transformation is mentioned: [Pg.181]    [Pg.23]    [Pg.508]    [Pg.69]    [Pg.457]    [Pg.308]    [Pg.1634]    [Pg.673]    [Pg.673]    [Pg.176]    [Pg.66]    [Pg.184]    [Pg.5]    [Pg.107]    [Pg.142]    [Pg.41]    [Pg.38]    [Pg.50]    [Pg.796]    [Pg.283]    [Pg.126]    [Pg.112]    [Pg.155]    [Pg.5]    [Pg.6]    [Pg.14]    [Pg.14]    [Pg.14]    [Pg.15]    [Pg.15]    [Pg.17]    [Pg.18]    [Pg.19]    [Pg.20]   
See also in sourсe #XX -- [ Pg.40 ]




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C-H Transformation in Industrial Processes

Handbook, of C-H Transformations. Gerald Dyker

Weber, H„ Oxidative Transformations

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