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41.
42.
Ivana Krausová Jan Kučera Ivo Světlík 《Journal of Radioanalytical and Nuclear Chemistry》2013,295(3):2043-2048
Neutron activation analysis (NAA) was used to determine 129I and the 129I/127I ratio in bovine thyroid, moss, and river sediment samples collected in the vicinity of the Temelín nuclear power plant (NPP) in south Bohemia. The NAA procedures comprised pre-irradiation separation of 129I by combustion of the samples in the stream of oxygen at 1,000 °C and trapping the liberated iodine in a LiOH/(NH4)2SO3 solution. Post-irradiation separation of 130I produced by the reaction 129I(n,γ)130I was carried out by extraction of elementary iodine with chloroform followed by precipitation of PdI2. Nondestructive, epithermal NAA was used to determine 127I employing the 127I(n,γ)128I reaction. The results showed that mean values of 129I and the 129I/127I ratio in the bovine thyroids varied from 22 to 61 mBq kg?1 (dry mass) and 2.8 × 10?9 to 5.4 × 10?9, respectively. These values are close to the lower end of results reported from various regions non-polluted with 129I. No significant differences were found between 129I concentrations and the 129I/127I ratios in the bovine thyroids collected prior to the start and after several years of operation of the NPP. The mean value and standard deviation of 129I in mBq kg?1, dry mass and the 129I/127I ratio in moss Pleurozium schreberi were 23 ± 16 and 2.3 × 10?9, respectively, whereas values of 129I in the river sediments were below 8–10 mBq kg?1 (dry mass) after several years of the NPP operation. 相似文献
43.
Lidia Alexandrova Michail Nedyalkov Dimo Platikanov Roberta Razzetti Federico Bianco 《Colloid and polymer science》2013,291(11):2725-2731
The wetting properties of pulmonary surfactant aqueous solutions with respect to solid surfaces with different degree of hydrophobicity have been studied. The contact angles θ of drops from a pulmonary surfactant solution onto SiO2-glass surfaces have been measured as a function of their degree of hydrophobicity θ w. The completely hydrophilic SiO2-glass surface is essentially hydrophobized by the animal-derived pulmonary surfactant Curosurf. The hydrophobization depends on the surfactant concentration—the contact angles increase with increasing the Curosurf concentration C s in the low concentration range, but they remain almost constant in a wide range of C s >90 μg/ml. Additions like NaCl and bovine serum albumin influence the θ-values. The contact angles θ naturally increase with increasing θ w but this dependence is not linear—the curve steepens at larger θ w values. The thickness h of the wetting thin liquid films from Curosurf aqueous solutions depends on the hydrophobicity θ w of the solid surface and the h(θ w) curves always pass a minimum. The h-values, as well as the h(θ w) curve, are mainly determined by the steric and hydrophobic disjoining pressures, which depend on the orientations and conformations of the molecules adsorbed on the solid surface from the very complicated multi-component aqueous solutions. 相似文献
44.
In this paper we report the first chemoselective asymmetric hydrogenation of (1-bromo-1-alkenyl)boronic esters, which constitutes a new route to (α-bromoalkyl)boronic esters. The study demonstrates that excellent chemoselectivities along with full conversions can be obtained for hydrogenation of alkyl substituted derivatives with iridium–PˆN complexes. Moreover, acyclic alkyl derivatives afford (α-bromoalkyl)boronic esters in good enantioselectivities ranging from 64 to 73% ee. A cyclic alkyl derivative was obtained only in a nearly racemic form. The (1-bromo-1-alkenyl)boronic esters appear to be less reactive towards homogenous hydrogenation conditions than their chloro analogues as demonstrated by the higher catalyst loadings required to achieve full conversions for alkyl derivatives and lower conversions observed for the aryl substituted derivatives. 相似文献
45.
Filip Botha Jan Budka Václav Eigner Oldřich Hudeček Lukáš Vrzal Ivana Císařová Pavel Lhoták 《Tetrahedron》2014
A new type of calixarene-based receptor designed for the recognition of chiral anions was prepared by the introduction of (S)-2-methylbutan-1-ol moieties into the lower rim of calixarene. The immobilization of calixarene skeleton in the 1,3-alternate conformation enabled the construction of a cavity consisting of preorganised ureido functions and chiral substituents in close proximity. This cavity is capable of chiral discrimination of selected anions as demonstrated on d- and l-phenylalaninates. 相似文献
46.
采用基于拉普拉斯算符聚焦形貌恢复方法,提出了模拟目标深度测量的数值模型。数值模拟的核心是基于通过几何光学预测的理想图像的卷积与透镜广义孔径函数的多色点扩散函数,即用聚焦误差替代抛物线圆柱形貌或高斯函数。该模型可以使用基于聚焦形貌恢复方法的传感器真实组件参数、光源光谱、光学系统离差、相机的光谱灵敏度。提出了光学系统离差(消球差、消色差、色差)对确定目标表面形貌的精确度和可靠性的影响。结果表明,该模型可以有效提高实验效率,缩短时滞,降低成本。 相似文献
47.
A. P. Kuznetsov A. S. Alexandrova O. I. Buzhinsky K. L. Gubskiy T. V. Kazieva A. V. Savchenkov S. N. Tugarinov 《Physics of Atomic Nuclei》2015,78(10):1155-1163
The results of experimental studies into efficiency of removal of films with a complex composition from metal mirrors by pulsed fiber laser irradiation are presented. It is shown that the initial reflectivity of optical elements can be restored by the selection of modes of irradiation impacting the surface with the sputtered film. Effective cleaning is performed by radiation with a power density lower than 107 W/cm2. The removal of contaminations at such a relatively low power density occurs in a solid phase, owing to which the thermal effect on the mirror is insignificant. 相似文献
48.
Juan M. Venegas Zisheng Zhang Theodore O. Agbi William P. McDermott Anastassia Alexandrova Ive Hermans 《Angewandte Chemie (International ed. in English)》2020,59(38):16527-16535
Boron‐containing materials, and in particular boron nitride, have recently been identified as highly selective catalysts for the oxidative dehydrogenation of alkanes such as propane. To date, no mechanism exists that can explain both the unprecedented selectivity, the observed surface oxyfunctionalization, and the peculiar kinetic features of this reaction. We combine catalytic activity measurements with quantum chemical calculations to put forward a bold new hypothesis. We argue that the remarkable product distribution can be rationalized by a combination of surface‐mediated formation of radicals over metastable sites, and their sequential propagation in the gas phase. Based on known radical propagation steps, we quantitatively describe the oxygen pressure‐dependent relative formation of the main product propylene and by‐product ethylene. Free radical intermediates most likely differentiate this catalytic system from less selective vanadium‐based catalysts. 相似文献
49.
50.
Fast simultaneous LC/MS/MS determination of 10 active compounds in human serum for therapeutic drug monitoring in psychiatric medication 下载免费PDF全文
Pavel Sistik Romana Urinovska Hana Brozmanova Ivana Kacirova Petr Silhan Karel Lemr 《Biomedical chromatography : BMC》2016,30(2):217-224
A UPLC/MS/MS method with simple protein precipitation has been validated for the fast simultaneous analysis of agomelatine, asenapine, amisulpride, iloperidone, zotepine, melperone, ziprasidone, vilazodone, aripiprazole and its metabolite dehydro‐aripiprazole in human serum. Alprenolol was applied as an internal standard. A BEH C18 (2.1 × 50 mm, 1.7 µm) column provided chromatographic separation of analytes using a binary mobile phase gradient (A, 2 mmol/L ammonium acetate, 0.1% formic acid in 5% acetonitrile, v/v/v; B, 2 mmol/L ammonium acetate, 0.1% formic acid in 95% acetonitrile, v/v/v). Mass spectrometric detection was performed in the positive electrospray ionization mode and ion suppression owing to matrix effects was evaluated. The validation criteria were determined: linearity, precision, accuracy, recovery, limit of detection, limit of quantification, reproducibility and matrix effect. The concentration range was as follows: 0.25–1000 ng/mL for agomelatine; 0.25–100 ng/mL for asenapine and iloperidone; 2.5–1000 ng/mL for amisulpride, aripiprazole, vilazodone and zotepine; 2.3–924.6 ng/mL for dehydroaripiprazole; 2.2–878.4 ng/mL for melperone; and 2.2–883.5 ng/mL for ziprasidone. Limits of quantitation below a therapeutic reference range were achieved for all analytes. Intra‐run precision of 0.4–5.5 %, inter‐run precision of 0.6–8.2% and overall recovery of 87.9–114.1% were obtained. The validated method was successfully implemented into routine practice for therapeutic drug monitoring in our hospital. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献