Moore. Standard

Source Samuel P. Moore, Standard Supply Table of the Indigenous Remedies for Field Servloe and the Slok In General Hospitals (RIohmond Surgeon General s Offloe , 1863). 

Source C. E. Moore, National Standard Reference Data Series 34, U.S. Government Printing Office, Washington, D.C.,... 

Size exclusion chromatography (SEC, also known as GPC and GFC) has become a very well accepted separation method since its introduction in the late-1950s by works of Porath and Flodin (1) and Moore (2). Polymers Standards Service (PSS) packings for SEC/SEC columns share this long-standing tradition as universal and stable sorbents for all types of polymer applications. In general, PSS SEC columns are filled with spherical, macroporous cross-linked, pressure-stable, and pH-resistant polymeric gels. 

Moore, C. E. Atomic Energy Levels Circular 457, National Bureau of Standards ... 

Moore, C. A. [1949] Atomic Energy Levels, U.S. Bureau of Standards, Washington, D.C. 

Moatti JP, Spire B, Kazatchkine M (2004) Drug resistance and adherence to HIV/AIDS antiretroviral treatment against a double standard between the north and the south, AIDS I8 S55-S6I Moore RD, Chaisson RE (1997) Costs to Medicaid of advancing immunosuppression in an urban HIV-infected patient population in Maryland, J Acquir Immune Defic Syndr Hum Retrovirol 16 223-231... 

Cali JP, Mandel J, Moore L, and Young DS (1972) A Referee Method for the Determination of Calcium in Serum Standard Reference Materials. NBS Spec Publ 260-36. National Bureau of Standards, Washington, DC. 

Although the energies of the spectroscopic states of first row d2 ions were shown in Table 18.4, compilations exist for all gaseous metal ions. The standard reference is a series of volumes published by the National Institute of Standards and Technology (C. E. Moore, Atomic Energy Levels, National Bureau of Standards Circular 467, Vol. I, II, and III, 1949). Table 18.5 shows the energies for the spectroscopic states in dn ions in terms of the Racah B and C parameters. 

Moore [355] used the solvent extraction procedure of Danielson et al. [119] to determine iron in frozen seawater. To a 200 ml aliquot of sample was added lml of a solution containing sodium diethyldithiocarbamate (1% w/v) and ammonium pyrrolidine dithiocarbamate (1 % w/v) at pH to 4. The solution was extracted three times with 5 ml volumes of 1,1,2 trichloro-1,2,2 trifluoroethane, and the organic phase evaporated to dryness in a silica vial and treated with 0.1 ml Ultrex hydrogen peroxide (30%) to initiate the decomposition of organic matter present. After an hour or more, 0.5 ml 0.1 M hydrochloric acid was added and the solution irradiated with a 1000 W Hanovia medium pressure mercury vapour discharge tube at a distance of 4 cm for 18 minutes. The iron in the concentrate was then compared with standards in 0.1 M hydrochloric acid using a Perkin-Elmer Model 403 Spectrophotometer fitted with a Perkin-Elmer graphite furnace (HGA 2200). 

Source C. E. Moore, National Standard Reference Data Series 34, U.S. Government Printing Office, Washington, D.C., 1970 W. C. Martin, Zalubas, R., and Hagan, L.,J. Phys. Chem. Reference Data, 3 771 (1974) and National Standard Reference Data Series, National Bureau of Standards (U S ), No. 60 (1978) for die Rare Earth Elements and Cohen, E. R. and Taylor, B. 

Mitchell PCH (1999) Molybdenum compounds. In Ullmann s Encyclopedia of Industrial Chemistry. Volume A16. Arpe H-J (ed) John Wiley and Sons, New York, p 675-82 Moore LJ, Machlan LA, Shields WR, Gamer EL (1974) Internal normalization techniques for high accurate isotope dilution analyses. Application to molybdenum and nickel in standard reference materials. Anal Chem 46 1082-1089... 

Ninhydrin assay. Our method to determine reactivity towards ninhydrin was a modification of a method described previously (Moore and Stein, 1954 Moore, 1968). Briefly, dried samples were dissolved in 0.10 ml 0.1 M acetic acid and mixed with an equal volume of ninhydrin reagent (Sigma). After 15 minutes in a boiling water bath, samples were diluted with 0.80 ml ethanol/water (1 1 by vol.) and measured for absorbance at 550 nm on a flow-through spectrophotometer (Vitatron). Standards containing 0-0.6 mM leucine in 0.1 M HAc were included. Values were therefore calculated as leucine-equivalents. 

Moore, M.M., Parker, L., Huston, J., Harrington-Brock, K. Dearfield, K.L. (1991) Comparison of mutagenicity results for nine compounds evaluated at the hgprt locus in the standard and suspension CHO assays. Mutagenesis, 6, 77-85... 

Valuer in kcal/moie. The values are obtained from the ionization potentials in Charlotte E. Moore, Atomic Energy Levels as Derived from the Analyses of Optical Spectra (Circular of the National Bureau of Standards 467, Government Printing Office, Washington, D. C.f 1949-1958, vol. Ill), by multiplying by the conversion factor from electron volts to kcal/mole, 23.053. 

W. H. Miller I would like to ask Prof. Schinke the following question. Regarding the state-specific unimolecular decay rates for HO2 — H + O2, you observe that the average rate (as a function of energy) is well-described by standard statistical theory (as one expects). My question has to do with the distribution of the individual rates about die average since there is no tunneling involved in this reaction, the TST/Random Matrix Model used by Polik, Moore and me predicts this distribution to be x-square, with the number of decay channels being the cumulative reaction probability [the numerator of the TST expression for k(E)] how well does this model fit the results of your calculations ... 

For convenience, the states that may arise by Russell-Saunders coupling from all dn configurations are listed in Table 9.1. For quantitative applications of ligand field theory we must know not only the nature of the states but also their relative energies in a particular ion. For a great number of the ions of practical interest these energies are known from experimental measurements. The standard tabulation of such data is C. E. Moore s Atomic Energy Levels. t... 

Moore, C. E. Ionization Potentials and Ionization Limits Derived from the Analyses of Optical Spectra, NSRDS-NBS 34 National Bureau of Standards Washington. DC, 1970, except for the data on the actinides, which are from The Chemistry ofthe Actinide Elements, Katz, J. J. Seaborg, G. T. Morss, L. R., Eds. Qiapman and Hall New York, 1986 Vol. 2. 

Moore. C. E. lorthaiion Potentials anti Ionization Linnrs Derived from the Analyses of Optical Spectra, NSRDS-NBS 34 National Bureeu of Standards Washington. DC. 1970. 

---