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61.
M. T. Sellers E. C. Corcoran D. G. Kelly 《Journal of Radioanalytical and Nuclear Chemistry》2013,295(2):1221-1228
The Royal Military College of Canada (RMCC) has commissioned a Delayed Neutron Counting (DNC) system for the analysis of special nuclear materials. A significant, time-dependent neutron background with an initial maximum count rate, more than 50 times that of the time-independent background, was characterised during the validation of this system. This time-dependent background was found to be dependent on the presence of the polyethylene (PE) vials used to transport the fissile samples, yet was not an activation product of vial impurities. The magnitude of the time-dependent background was found to be irradiation site specific and independent of the mass of PE. The capability of RMCC’s DNC system to analyze the neutron count rates in time intervals <1 s facilitated a more detailed data analysis than that obtained in previous DNC systems recording cumulative neutron counts. An analysis of the time-dependent background behaviour suggested that an equivalent of 120 ng of 235U contamination was present on each irradiated vial. However, Inductively Coupled Plasma—Mass Spectroscopy measurements of material leached from the outer vial surfaces after their irradiations found only trace amounts of uranium, 0.118 ± 0.048 ng of 235U derived from natural uranium. These quantities are insufficient to account for the time-independent background, and in fact could not be discriminated from the noise associated with time-independent background. It is suggested that delayed neutron emitters are deposited in the vial surface following fission recoil, leaving the main body of uranium within the irradiation site. This hypothesis is supported by the physical cleaning of the site with materials soaked in distilled water and HNO3, which lowered the background from a nominal 235U mass equivalent of 120 to 50 ng per vial. 相似文献
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George E. Andrews Donny Passary James A. Sellers Ae Ja Yee 《The Ramanujan Journal》2017,42(2):347-361
We establish new connection formulae between Fibonacci polynomials and Chebyshev polynomials of the first and second kinds. These formulae are expressed in terms of certain values of hypergeometric functions of the type \(_2F_{1}\). Consequently, we obtain some new expressions for the celebrated Fibonacci numbers and their derivative sequences. Moreover, we evaluate some definite integrals involving products of Fibonacci and Chebyshev polynomials. 相似文献
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The nature of sulfate-Ag(111) and sulfate-Au(111) surface bonding has been investigated at the SCF + MP2 level of theory. Convergence of binding energy with cluster size is investigated and, unlike neutral adsorbates, large clusters are required in order to obtain reliable binding energies. In the most stable adsorption mode, sulfate binds to the surface via three oxygen atoms (C3v symmetry) with a binding energy of 159.3 kcal/mol on Ag(111) and 143.9 kcal/mol on Au(111). The geometry of adsorbed sulfate was optimized at the SCF level. While the bond length between sulfur and the oxygens coordinated to the surface increases, the sulfur-uncoordinated oxygen bond length decreases. This weakening and strengthening of the bonds, respectively, is consistent with bond order conservation in adsorbates on metal surfaces. Although a charge transfer of 0.4 electrons towards the metal is observed, the adsorbate remains very much sulfate-like. The molecular orbital analysis indicates that there is also some charge back-donation towards unoccupied orbitals of sulfate. This results in an increased electron density around sulfur as revealed in the electron density difference maps. Analysis of the Laplacian of the charge density of free sulfate provides a suitable framework to understand the nature of the different charge transfer processes and allows us to establish some similarities with the CO- and SO2-metal bondings. 相似文献
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Dr. Sumith A. Kularatne Dr. Vishal Deshmukh Dr. Jennifer Ma Dr. Virginie Tardif Dr. Reyna K. V. Lim Holly M. Pugh Dr. Ying Sun Anthony Manibusan Aaron J. Sellers Dr. Richard S. Barnett Shailaja Srinagesh Jane S. Forsyth Dr. Wolf Hassenpflug Dr. Feng Tian Dr. Tsotne Javahishvili Prof. Brunhilde Felding‐Habermann Prof. Brian R. Lawson Dr. Stephanie A. Kazane Prof. Peter G. Schultz 《Angewandte Chemie (International ed. in English)》2014,53(44):11863-11867
A chemically defined anti‐CXCR4–auristatin antibody–drug conjugate (ADC) was synthesized that selectively eliminates tumor cells overexpressing the CXCR4 receptor. The unnatural amino acid p‐acetylphenylalanine (pAcF) was site‐specifically incorporated into an anti‐CXCR4 immunoglobulin G (IgG) and conjugated to an auristatin through a stable, non‐cleavable oxime linkage to afford a chemically homogeneous ADC. The full‐length anti‐CXCR4 ADC was selectively cytotoxic to CXCR4+ cancer cells in vitro (half maximal effective concentration (EC50)≈80–100 pM ). Moreover, the anti‐CXCR4 ADC eliminated pulmonary lesions from human osteosarcoma cells in a lung‐seeding tumor model in mice. No significant overt toxicity was observed but there was a modest decrease in the bone‐marrow‐derived CXCR4+ cell population. Because CXCR4 is highly expressed in a majority of metastatic cancers, a CXCR4–auristatin ADC may be useful for the treatment of a variety of metastatic malignancies. 相似文献
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