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21.
Heat capacities of concentrated multicomponent aqueous electrolyte solutions at various temperatures
Boris S. Krumgalz Ilan A. Malester Irving J. Ostrich Frank J. Millero 《Journal of solution chemistry》1992,21(7):635-649
The specific heat capacities of the aqueous multicomponent system NaCl +KCl+MgCl2+CaCl2 with ionic strength between 8.3 and 9.6 (resembling Dead Sea waters) were measured between 15°C and 45°C. The obtained data were fitted to an empirical equation as a function of concentration and temperature. The thermodynamic functions of the studied multicomponent system were found to be strongly influenced by changes in MgCl2 concentrations. The application of Young's rule to such concentrated systems was checked at 25°C. The calculated (by Young's rule) specific heat capacitiesC
p and apparent molar heat capacities Cp, of these multicomponent electrolyte solutions were in reasonable agreement with the measured values (–0.008 J-g–1-K–1 and –2.6 J-mol–1-K–1, respectively). 相似文献
22.
The present work describes the synthesis of the beta-isomer of 1-alpha-D-(5-deoxy-5-iodoarabinofuranosyl)-2-nitroimidazole (IAZA). Radioiodinated IAZA ((123)I-IAZA) has been extensively studied as a radiopharmaceutical for the diagnosis of regional and/or focal tissue hypoxia in a variety of clinical pathologies. The beta-anomer of IAZA, 1-beta-D-(5-deoxy-5-iodoarabinofuranosyl)-2-nitroimidazole (beta-IAZA, 1), was synthesized via an unconventional route starting from 1-beta-D-(ribofuranosyl)-2-nitroimidazole (AZR), with a change of configuration at the C-2'-position to afford 1-beta-D-(arabinofuranosyl)-2-nitroimidazole (beta-AZA, 7). Nucleophilic iodination of the 5'-O-toluenesulfonyl-2',3'-di-O-acetyl precursor of beta-AZA, 9, followed by deprotection, afforded 1 in satisfactory yield. beta-IAZA (1) was also synthesized from 7 using molecular iodine and triphenylphosphine. 相似文献
23.
This paper presents a short synthesis of oncinotin-11-one ( 11 ), a minor alkaloid of Oncinotis tenuiloba (Apocynaceae). Based on a disconnection approach, the spermidine portion of the key intermediate 6 was constructed consecutively by simple N-alkylations starting from ethyl piperidine-2-carboxylate ( 1 ). Treatment of 6 with in situ lithiated 2-[(10-bromodecyl)oxy]tetrahydropyran resulted in the formation of the keto moiety under simultanous deprotection of the lactam N-atom to give the amino ketone 7 in 71% yield. Cleavage of the tetrahydro-2H-pyran-2-yl(Thp) portion and Jones oxidation of the resulting alcohol 8 gave the amino acid 9 which was cyclized. Final N-debenzylation of 10 provided the natural alkaloid 11 . Only two protective groups were needed in this synthesis. The reaction of N-alkyl-lactams with organometallic reagents is discussed. 相似文献
24.
Metal‐pernitride compounds belong to a class of chemical systems in which both the complex ions and the non‐bonding electrons may play roles in the formation of their modified crystalline structures. To investigate this issue, the energy landscapes of pernitrides of metals with different maximum valence (M=Ca, Sr, Ba, La, and Ti) were globally explored on the ab initio level at standard and high pressures, thereby yielding possible (meta)stable modifications in these systems together with information on how the landscape changed as function of the valence of the metal cation. For all of the systems in which no compounds had been synthesized so far, we predicted the existence of kinetically stable modifications that should, in principle, be experimentally accessible. In particular, TiN2 should crystallize in a new structure type, TiN2‐I. 相似文献
25.
M. Talebi-Esfandarani S. Rousselot M. Gauthier P. Sauriol G. Liang M. Dollé 《Journal of Solid State Electrochemistry》2016,20(7):1821-1829
LiFePO4/C material has been prepared using fast-melt synthesis method followed by grinding and carbon coating. The low-cost iron ore concentrate (IOC) and purified iron ore concentrate (IOP) were used as iron precursors in the melt process to reduce significantly the cost of LiFePO4/C. The same product was also synthesized using pure Fe2O3 under similar conditions as reference. The physical-chemical and electrochemical properties of samples were investigated. The X-ray Diffraction (XRD) results confirm the formation of an olivine structure of LiFePO4 with a minor amount of Li3PO4 and Li4P2O7 impurities for all the samples but no Fe2P. The power performances of LiFePO4/C using low-cost iron precursors were close to the sample using pure Fe2O3 precursor although capacity in mAh g?1 is somewhat lower. With the inherent presence of silicon and other metals species, multi-substitution may take place when using IOC as source of iron leading to a Li(Fe1-yMy)(P1-xSix)O4 general composition. Multi-substitution, however, allows a better cycling stability. Therefore, these iron precursors present a promising option in this field to reduce the cost of a large-scale synthesis of LiFePO4/C for Li-ion batteries application. 相似文献
26.
Eladio Rodriguez‐Diaz Danielle Manolakos Holly Christman Michael A. Bonning John K. Geisse Ousama M. A'Amar David J. Leffell Irving J. Bigio 《Photochemistry and photobiology》2019,95(6):1441-1445
Skin cancer is the most prevalent cancer, and its assessment remains a challenge for physicians. This study reports the application of an optical sensing method, elastic scattering spectroscopy (ESS), coupled with a classifier that was developed with machine learning, to assist in the discrimination of skin lesions that are concerning for malignancy. The method requires no special skin preparation, is non‐invasive, easy to administer with minimal training, and allows rapid lesion classification. This novel approach was tested for all common forms of skin cancer. ESS spectra from a total of 1307 lesions were analyzed in a multi‐center, non‐randomized clinical trial. The classification algorithm was developed on a 950‐lesion training dataset, and its diagnostic performance was evaluated against a 357‐lesion testing dataset that was independent of the training dataset. The observed sensitivity was 100% (14/14) for melanoma and 94% (105/112) for non‐melanoma skin cancer. The overall observed specificity was 36% (84/231). ESS has potential, as an adjunctive assessment tool, to assist physicians to differentiate between common benign and malignant skin lesions. 相似文献
27.
28.
Irving H. Anellis 《Logica Universalis》2012,6(3-4):301-326
Van Heijenoort??s account of the historical development of modern logic was composed in 1974 and first published in 1992 with an introduction by his former student. What follows is a new edition with a revised and expanded introduction and additional notes. 相似文献
29.
Charles Doll Erin Finn Michael Cantaloub Larry Greenwood Jeremy Kephart Rosara F. Kephart 《Journal of Radioanalytical and Nuclear Chemistry》2013,295(1):331-334
Neutron activation of gas samples in a reactor often requires a medium to retain sufficient amounts of the gas for analysis. Charcoal is commonly used to adsorb gas and hold it for activation; however, the amount of activated sodium in the charcoal after irradiation swamps most signals of interest. Neutron activation analysis was performed on several commonly available charcoal samples in an effort to determine the activation background. The results for several elements, including the dominant sodium element, are reported. It was found that ECN charcoal had the lowest elemental background, containing sodium at 2.65 ± 0.05 ppm, as well as trace levels of copper and tungsten. 相似文献
30.
Huiyun Jiang Yameng Ren Weiwei Zhang Yongzhen Wu Etienne Christophe Socie Brian Irving Carlsen Jacques‐E. Moser He Tian Shaik Mohammed Zakeeruddin Wei‐Hong Zhu Michael Grtzel 《Angewandte Chemie (International ed. in English)》2020,59(24):9324-9329
Dye‐sensitized solar cells (DSSCs) based on CuII/I bipyridyl or phenanthroline complexes as redox shuttles have achieved very high open‐circuit voltages (VOC, more than 1 V). However, their short‐circuit photocurrent density (JSC) has remained modest. Increasing the JSC is expected to extend the spectral response of sensitizers to the red or NIR region while maintaining efficient electron injection in the mesoscopic TiO2 film and fast regeneration by the CuI complex. Herein, we report two new D‐A‐π‐A‐featured sensitizers termed HY63 and HY64 , which employ benzothiadiazole (BT) or phenanthrene‐fused‐quinoxaline (PFQ), respectively, as the auxiliary electron‐withdrawing acceptor moiety. Despite their very similar energy levels and absorption onsets, HY64 ‐based DSSCs outperform their HY63 counterparts, achieving a power conversion efficiency (PCE) of 12.5 %. PFQ is superior to BT in reducing charge recombination resulting in the near‐quantitative collection of photogenerated charge carriers. 相似文献