Application of Atkinson

Handgnn permit Application of Atkinson Schubert v. DeBard Intoxication and weapons use City of Salina v. Blaksley Kitchen v. K-Mart... 

Atkinson TC, Rowe PJ (1992) Applications of dating to denudation chronology and landscape evolution. In Uranium-series disequilibriiun Applications to Earth, Marine and Enviromnental Sciences, Ivanovich M, Harmon RS (eds) Oxford University Press, Oxford, p 669-703 Auler AS, Smart PL (2001) Late Quaternary paleoclimate in semiarid Northeastern Brazil from U-series dating of travertines and water table speleothems. Quat Res 55 159-167 Ayliffe LK, Marianelh PC, Moriarty KC, Wells RT, McCulloch MT, Mortimer GE, Hellstrom JC (1998) 500 ka precipitation record from southeastern Australia Evidence for interglacial relative aridity. Geology 26 147-150... 

Reported applications of DST include the crosslinking of ubiquinone cytochrome C reductase (Smith et al., 1978), characterization of the cell surface receptor for colony-stimulating factor (Park et al., 1986), investigation of the Ca+2-, Mg+2-activated ATP of E. coli (Bragg and Hou, 1980), and characterization of human properdin polymers (Farries and Atkinson, 1989). 

R.L. Airs, J.E. Atkinson and B.J. Keely, Development and application of a high resoltuion liquid chromatographic method for the analysis of complex pigment distributions. J. 

Ian Atkinson is based at lames Cook University in Queensland where his research interests lie in the application of high performance computing tochemkal problems. He has undertaken computational studies across a number of areas that include thermodynamic and chemical aspects of transition metal binding to substrates, self-assembly in supramoiecular chemistry and crystal engineenng... 

Atkinson, T.C. and Rowe, P.J., 1992, Application of dating to denudation chronology and landscape evolution, in Uranium-Series Disequilibrium, (2" ed.) M. Ivanovich and R.S. Harmon, eds.. Clarendon Press, Oxford, pp.670-703. 

No doubt in all real cases there will be a distribution of diameters d. This difficulty can be avoided by using Equ. 3.28 to calculate an average diameter dp for a particular distribution function (Atkinson and Ur-Rahman, 1979). The further application of dp for evaluating the extent of transport-limiting factors is described in Sect. 4.5.2. Biofilm reactors with mechanical or hydro-dynamic control of film thickness exhibit a uniform dp and thus are more suitable than floe bioreactors for process kinetic analyses (see Sects. 3.6 and 4.3). 

Atkinson JG, Girard Y, Rokach J, Rooney CS, Me Farlane CS, Rackham A, Share NN (1979) Kojic amine-a novel gamma-aminobutyric acid analogue. J Med Chem 22 99-106 Meanwell NA (2011) Synopsis of some recent tactical application of bioisosteres in drug design. J Med Chem 54 2529-2591... 

The Mode III problem has received most attention essentially because it is the simplest case. Mode I and II problems are considerably more difficult, but have been considered in a limiting case by Atkinson (1979), and again using an exact, partly numerical application of the Wiener-Hopf method, by Popelar and Atkinson (1980). But the physical Importance of the Mode III problem is cast into doubt by experimental observations of Knauss (1970 b) indicating that such cracks do not grow rectilinearly, at least in brittle materials. 

Atkinson R, Gibson V, Long N. The syntheses and catalytic applications of unsymmetrical ferrocene ligands. Chem. Soc. Rev. 2004 33 313-328. 

Reaction of butanal with all three reactive species leads primarily to the formation of the butanoyl radical by abstraction of the aldehydic H-atom. Papagni et al. (2000) noted an increase in the rate coefficient of OH with butanal, compared with that with propanal, which is compatible with the sensitization of the C—H bond to the carbonyl group proposed by Kwok and Atkinson (1995). Application of their structure-activity relations (SARs) gives 17% abstraction at this site with a channel yield of 78% for production of the acyl radical. Reaction of the acylperoxy radical with NO2 forms peroxybutanoyl nitrate, while reaction with NO forms CO2 and the -propyl radical, which then reacts with O2 to form the n-propylperoxy radical, whose main atmospheric fate is conversion to propanal. 

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