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21.
ABSTRACTIn this paper, lanthanum was used as a chemical modifier for the direct determination of erbium by high-resolution continuum source electrothermal atomic absorption spectrometry. A two-step experimental design was used for optimization, first a full factorial design was conducted for identification of significant factors, and then a central composite design was carried out for final optimization of the significant factors. The optimum parameters were obtained as follows: atomization temperature of 2500°C, pyrolysis temperature of 1600°C, and pyrolysis time of 10?s in the presence of lanthanum as a chemical modifier. Under optimum conditions, the characteristic mass, limit of detection, and limit of quantification were 29?pg, 0.71, and 2.4?µg?L?1, respectively. The precision of the method, estimated as the relative standard deviation for 10 replicate measurements of 50?µg?L?1 of erbium, was 1.8%. The optimized method was applied to determine erbium content in sediments and rock samples. The determined values of erbium in sediment certified reference materials were in satisfactory agreement with the certified values according to the t-test for a 95% confidence level. 相似文献
22.
Sajjad Uzair Hussain Imtiyaz Hamid Khalid Bhat Showkat Ahmad Ali Hafiz Muhammad Wang Chi-Chuan 《Journal of Thermal Analysis and Calorimetry》2021,145(4):1911-1923
Journal of Thermal Analysis and Calorimetry - Owing to the high nucleation site density and relatively robust behavior, sintered coated surfaces are of great interest for thermal management via... 相似文献
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Pouretedal Hamid Reza Damiri Sajjad Sharifi Alireza 《Journal of Thermal Analysis and Calorimetry》2020,139(1):545-553
Journal of Thermal Analysis and Calorimetry - The polymorphs of HMX explosive show the different sensitivities to heat, friction, impact, shock, electrostatic charge, etc. Knowledge and... 相似文献
25.
In the present work, an innovative leach proof nanocatalyst based on dendritic fibrous nanosilica (DFNS) modified with ionic liquid loaded Fe3O4 NPs and CuI salts was designed and applied for the rapid synthesis of imidazo[1,2‐a]pyridines from the reaction of phenyl acetylene, 2‐aminopyridine, and aldehydes in aqueous medium. The structure of the synthesized nanocatalyst was studied by field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), Fourier transform infrared (FT‐IR), flame atomic absorption spectroscopy (FAAS), energy‐dispersive X‐ray (EDX), and X‐ray diffraction (XRD), vapor–liquid–solid (VLS), and adsorption/desorption analysis (Brunauer–Emmett–Teller [BET] equation) instrumental techniques. CuI/Fe3O4NPs@IL‐KCC‐1 with high surface area (225 m2 g?1) and porous structure not only exhibited excellent catalytic activity in aqueous media but also, with its good stability, simply recovered by an external magnet and recycled for eight cycles without significant loss in its intrinsic activity. Higher catalytic activity of CuI/Fe3O4NPs@IL‐KCC‐1 is due to exceptional dendritic fibrous structure of KCC‐1 and the ionic liquid groups that perform as strong anchors to the loaded magnetic nanoparticles (MNPs) and avoid leaching them from the pore of the nanocatalyst. Green reaction media, shorter reaction times, higher yields (71–97%), easy workup, and no need to use the chromatographic column are the advantages of the reported synthetic method. 相似文献
26.
Sajjad H. Sumrra Abrar U. Hassan Muhammad Imran Muhammad Khalid Ehsan U. Mughal Muhammad N. Zafar Muhammad N. Tahir Muhammad A. Raza Ataualpa A.C. Braga 《应用有机金属化学》2020,34(7):e5623
This study reports the synthesis of sulfonamide-derived Schiff bases as ligands L 1 and L 2 as well as their transition metal complexes [VO(IV), Fe(II), Co(II), Ni(II), Cu(II), and Zn(II)]. The Schiff bases (4-{E-[(2-hydroxy-3-methoxyphenyl)methylidene]amino}benzene-1-sulfonamide ( L 1 ) and 4-{[(2-hydroxy-3-methoxyphenyl)methylidene]amino}-N-(5-methyl-1,2-oxazol-3-yl)benzene-1-sulfonamide ( L 2 ) were synthesized by the condensation reaction of 4-aminobenzene-1-sulfonamide and 4-amino-N-(3-methyl-2,3-dihydro-1,2-oxazol-5-yl)benzene-1-sulfonamide with 2-hydroxy-3-methoxybenzaldehyde in an equimolar ratio. Sulfonamide core ligands behaved as bidentate ligands and coordinated with transition metals via nitrogen of azomethine and the oxygen of the hydroxyl group. Ligand L 1 was recovered in its crystalline form and was analyzed by single-crystal X-ray diffraction technique which held monoclinic crystal system with space group (P21/c). The structures of the ligands L 1 and L 2 and their transition metal complexes were established by their physical (melting point, color, yields, solubility, magnetic susceptibility, and conductance measurements), spectral (UV–visible [UV–Vis], Fourier transform infrared spectroscopy, 1H NMR, 13C NMR, and mass analysis), and analytical (CHN analysis) techniques. Furthermore, computational analysis (vibrational bands, frontier molecular orbitals (FMOs), and natural bonding orbitals [NBOs]) were performed for ligands through density functional theory utilizing B3LYP/6-311+G(d,p) level and UV–Vis analysis was carried out by time-dependent density functional theory. Theoretical spectroscopic data were in line with the experimental spectroscopic data. NBO analysis confirmed the extraordinary stability of the ligands in their conjugative interactions. Global reactivity parameters computed from the FMO energies indicated the ligands were bioactive by nature. These procedures ensured the charge transfer phenomenon for the ligands and reasonable relevance was established with experimental results. The synthesized compounds were screened for antimicrobial activities against bacterial (Streptococcus aureus, Bacillus subtilis, Eshcheria coli, and Klebsiella pneomoniae) species and fungal (Aspergillus niger and Aspergillus flavous) strains. A further assay was designed for screening of their antioxidant activities (2,2-diphenyl-1-picrylhydrazine radical scavenging activity, total phenolic contents, and total iron reducing power) and enzyme inhibition properties (amylase, protease, acetylcholinesterase, and butyrylcholinesterase). The substantial results of these activities proved the ligands and their transition metal complexes to be bioactive in their nature. 相似文献
27.
Elham Safaei Sajjad Mohebbi Mehdi Irani 《Journal of Sol-Gel Science and Technology》2018,86(1):170-174
TiO2/WO3 nanocomposite with nanodisk morphology was prepared and successfully used as a photocatalyst. The nanocomposite was obtained via sonochemical and hydrothermal methods, using pomegranate juice as a capping agent. The products were characterized by FE-SEM imaging, BET, EDAX spectroscopy, X-ray diffraction, DRS, and FT-IR spectroscopy. TiO2/WO3 nanocomposite showed high sensitivity to absorb visible light in compared to TiO2. In an optimized condition, the yield of the aerobic photocatalytic oxidation of benzyl alcohol derivatives reached to 65% for the TiO2/WO3 nanocomposite, while the conversion percent of the derivatives was less than 8% and 50% on the TiO2 and WO3 nanoparticles, respectively. Experimental results were supported by density functional theory (DFT) calculations. The DFT results in several solvents of different dielectric constants, confirmed the strong dependence of light absorption and photocatalytic activity to adsorption energy of the substrates on the surface of the nanoparticles (Ead). In addition, the theoretical results showed an inverse correlation between the adsorption energy of benzyl alcohol and its conversion percent, accordance to the experimental trend. 相似文献
28.
Back Cover: Integrated Transmission Electron and Single‐Molecule Fluorescence Microscopy Correlates Reactivity with Ultrastructure in a Single Catalyst Particle (Angew. Chem. Int. Ed. 1/2018) 下载免费PDF全文
29.
Integrated Transmission Electron and Single‐Molecule Fluorescence Microscopy Correlates Reactivity with Ultrastructure in a Single Catalyst Particle 下载免费PDF全文
Frank C. Hendriks Sajjad Mohammadian Dr. Zoran Ristanović Dr. Sam Kalirai Dr. Florian Meirer Prof. Dr. Eelco T. C. Vogt Dr. Pieter C. A. Bruijnincx Prof. Dr. Hans C. Gerritsen Prof. Dr. Bert M. Weckhuysen 《Angewandte Chemie (International ed. in English)》2018,57(1):257-261
Establishing structure–activity relationships in complex, hierarchically structured nanomaterials, such as fluid catalytic cracking (FCC) catalysts, requires characterization with complementary, correlated analysis techniques. An integrated setup has been developed to perform transmission electron microscopy (TEM) and single‐molecule fluorescence (SMF) microscopy on such nanostructured samples. Correlated structure–reactivity information was obtained for 100 nm thin, microtomed sections of a single FCC catalyst particle using this novel SMF‐TEM high‐resolution combination. High reactivity in a thiophene oligomerization probe reaction correlated well with TEM‐derived zeolite locations, while matrix components, such as clay and amorphous binder material, were found not to display activity. Differences in fluorescence intensity were also observed within and between distinct zeolite aggregate domains, indicating that not all zeolite domains are equally active. 相似文献
30.
Density functional theory calculations on complexes of 4C1, 1C4 and 2SO ring conformations of methyl beta-D-xylopyranoside 1 with divalent metal cations, M = Mg2+, Ca2+, Zn2+, and Cd2+, are presented. Bridging and pendant cationic, [M(H2O)41]2+ and [M(H2O)(5)1]2+, as well as neutral complexes, [M(OH)2(H2O)(2)1] and [M(OH)2(H2O)(3)1], and neutral complexes involving a doubly deprotonated sugar, [M(H2O)(4)1(2-)], are considered. In aqueous and chloroform solution the stability of cationic and pendant neutral complexes is greatly diminished compared with gas-phase results. In contrast, bridging neutral complexes [M(OH)2(H2O)(2)1] and those of type [M(H2O)(4)1(2-)], are stabilized with increasing solvent polarity. Solvation also profoundly influences the preferred binding position and ring conformation. Compared with complexes of bare metal cations, additional ligands, e.g., H2O or OH-, significantly reduce the stability of 1C4 ring complexes. Irrespective of the cation, the most stable structure of bridging complexes [M(H2O)(4)1]2+ results from coordination of the metal to O3 and O4 of methyl beta-D-xylopyranoside in its 4C1 ring conformation. 相似文献