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111.
Reed M. Izatt Robert M. Haws John D. Lamb David V. Dearden Philip R. Brown Don W. McBride Jr. James J. Christensen 《Journal of membrane science》1984,20(3):273-284
Cation fluxes were determined for various three-component, equimolar mixtures of alkali metal, alkaline earth, and Pb2+ cations in a H2O---CHCl3---H2O liquid membrane system incorporating macrocyclic polyethers as carriers. Carrier ligands studied were 18-crown-6, dicyclohexano-18-crown-6, 1,10-diaza-18-crown-6, 21-crown-7, dibenzo-24-crown-8, and cryptand [2.2.2]. Correlations were found between transport and relative cation:polyether cavity radii, the type of substituents present on the polyether ring, and the type and number of donor atoms present. All the ligands studied transported Pb2+ at higher rates than the other Mn+ in the mixtures. Transport behavior in these multi-cation systems can be predicted from Mn+—polyether complex stability constant data in most cases. 相似文献
112.
Traceability is not always evident in proficiency testing programs, although this is a requirement in ISO/IEC Guide 43-1. The assigned, or "true", value in most programs is not traceable to an independent entity. The test materials should generally be similar in nature to those routinely tested by participating laboratories. This is far from always the case and it is important to realize that if the difference is large, there may be no traceability to the testing program. It is also important that results from participation in proficiency tests are cited when papers are published, in order to enhance reliability/credibility of the published data.
相似文献113.
The First Polyiodo Complex – Triethylsulfoniumtriiodomercurate(II)-tris(diiodine), (Et3S)[Hg2I6]1/2 · 3 I2 After Raman spectroscopic investigation of the system HgI2/Et3SIx, x = 3, 5, 7, triethylsulfoniumtriiodomercuratetris(diiodine), (Et3S)[Hg2I6]1/2 · 3 I2 was synthesized by reacting of HgI2 and liquid Et3SI7. The compound crystallizes at room temperature triclinically in the space group P1 with a = 879.4(7), b = 1 209.1(5), c = 1 291.5(5) pm, α = 96.16(3)°, β = 103.82(6)°, γ = 99.05(5)° and Z = 2. The crystal structure is composed of disordered Et3S+ cations, the centrosymmetric complex anion [HgI2/2I2]22? and three connecting iodine molecules I2. 相似文献
114.
Coupling rates between the radicals methyl, n-, sec-, tert-butyl and benzyl (R.) and the aromatic radical anions of 1,4-dicyanonaphthalene, 9,10-dicyanoanthracene and fluorenone (A-.) have been obtained using a new laser-flash photolysis method. The radicals R. and the radical anions A-. were generated by a photoinduced electron transfer reaction between the aromatic compound A and the alkyl or benzyl triphenylborate anion RB(Ph)3-. For the first time the rate constants of the coupling reaction between methyl and benzyl radicals with aromatic radical anions have been obtained. For all the measured coupling rate constants an average value of k1 = 1.9 x 10(9) M-1 s-1 was found with a relatively small variation in the coupling rates (0.8-2.9 x 10(9) M-1 s-1). The results demonstrate that the coupling rate k1 is insensitive to changes in the steric and electronic properties of the radicals and the structure and standard potentials of the aromatic radical anions. 相似文献
115.
Rodrigues Filipe Agra Agostinho Hvattum Lars Magnus Requejo Cristina 《Journal of Heuristics》2021,27(3):459-496
Journal of Heuristics - Proximity search is an iterative method to solve complex mathematical programming problems. At each iteration, the objective function of the problem at hand is replaced by... 相似文献
116.
The use of polymeric amines to enhance the mechanical properties of lignocellulosic fibrous networks
Cationic polyelectrolytes (polyallylamine and polyvinylamine with different molecular masses) were adsorbed onto lignocellulosic fibres from unbleached and unbeaten spruce chemical fibres with different kappa numbers to investigate the effects on the mechanical properties of the final paper materials. Adsorption isotherms were first established to determine the maximum quantity of polymer that could be adsorbed onto each type of fibre. Paper sheets were then made with different amounts of added polyelectrolyte, and the structural and mechanical properties of the sheets were investigated, as well as the effect of an extra heating. The use of fibres with different kappa numbers led to different responses in terms of adsorption, and thus to differences in the mechanical properties of the resulting sheets. The tensile strength index was significantly increased (almost 50 % improvement in the best case) as a consequence of this polyelectrolyte adsorption onto the fibres, even at as low an adsorption level as 2 mg/g. The heating of paper sheets for 10 min at 160 °C was also shown to improve the tensile strength index by about 10 % for pulps with high kappa number. 相似文献
117.
Lars Rummel Jan M. Schümann Prof. Dr. Peter R. Schreiner 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(55):13699-13702
We present a computational analysis of hexaphenylethane derivatives with heavier tetrels comprising the central bond. In stark contrast to parent hexaphenylethane, the heavier tetrel derivatives can readily be prepared. In order to determine the origin of their apparent thermodynamic stability against dissociation as compared to the carbon case, we employed local energy decomposition analysis (LED) and symmetry-adapted perturbation theory (SAPT) at the DLPNO-CCSD(T)/def2-TZVP and sSAPT0/def2-TZVP levels of theory. We identified London dispersion (LD) interactions as the decisive factor for the molecular stability of heavier tetrel derivatives. This stability is made possible owing to the longer (than C−C) central bonds that move the phenyl groups out of the heavily repulsive regime so they can optimally benefit from LD interactions. 相似文献
118.
George Pitsevich Elena Shalamberidze Alex Malevich Valdas Sablinskas Vytautas Balevicius Lars G. M. Pettersson 《Molecular physics》2017,115(20):2605-2613
The frequencies and intensities of vibration–rotational transitions of water molecules in an argon matrix were calculated for temperatures of 6 and 30 K. The rigid asymmetric top approximation was used with available literature values of the effective rotational constants in the ground and excited vibrational states. The calculations were carried out by taking into account the existence of a non-equilibrium population distribution between the rotational levels of ortho- and para-water isomers. It was assumed that the temperature relaxation of the population of rotational levels is independent of the ortho- and para-isomers. Comparison of the results of the theoretical calculations with experimental literature data shows good agreement for the majority of the rotational structure lines for symmetric and antisymmetric stretching vibrations both in the frequency values and in the values of the relative intensities. 相似文献
119.
Falko Böttger‐Hiller Patrick Kempe Dr. Gerhard Cox Dr. Alexander Panchenko Dr. Nicole Janssen Dr. Albrecht Petzold Prof. Dr. Thomas Thurn‐Albrecht Lars Borchardt Dr. Marcus Rose Prof. Dr. Stefan Kaskel Colin Georgi Prof. Dr. Heinrich Lang Prof. Dr. Stefan Spange 《Angewandte Chemie (International ed. in English)》2013,52(23):6088-6091