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1.
2.
Duolite GT-73 resin was used for the preconcentration of Hg(II) from hydrochloric acid media as well as separation of the analyte from diversity of the co-existing metal ions (Al, Ca, Cd, Co, Cr, Cu, Fe, Mg, Mn, Ni, Pb and Zn) in off-line column operation. Due to the high affinity of the resin to the transition metals, Hg was adsorbed alongside with the foreign metals investigated. A complete release of the concomitant metals from the resin without the desorption of Hg was carried out using solutions of HCl and HNO3. A quantitative recovery of Hg was obtained by digestion of the resin using a H2SO4 and H2O2 mixture in an open-vessel system. An enrichment factor of 40 was achieved. The devised procedure was applied for the determination of Hg(II) in tap-water samples. 相似文献
3.
A notion of anin-tree is introduced. It is then used to characterize and count plane embeddings of outerplanar graphs. In-trees have also been applied in the study of independent vertex covers of faces in outerplanar graphs.This research was partially supported by the grant RP.I.09, from the Institute of Informatics, University of Warsaw. Hospitality of the Institute of Datalogy, University of Copenhagen where this research has been completed is gratefully acknowledged. 相似文献
4.
Pawel Hitczenko 《Probability Theory and Related Fields》1988,78(2):223-230
Summary It is shown that for all tangent sequences (d
n) and (e
n) of nonnegative or conditionally symmetric random variables and for every function satisfying the growth condition (2x)(x) the following inequality holds:
. This generalizes results of J. Zinn and proves a conjecture of S. Kwapie and W.A. Woyczyski. 相似文献
5.
Marek Szymo
ski Jacek Ko
odziej Zbigniew Postawa Pawel Czuba Piotr. Piatkowski 《Progress in Surface Science》1995,48(1-4):83-96
Inelastic interactions of electrons with surfaces of ionic crystals result in emission of various particles such as ions, atoms and molecules. We will review such electron-stimulated desorption processes for the particular class of ionic crystals, namely for alkali halides. In this case, a dominant fraction of the emission is in the form of halogen and alkali atoms characterized by a thermal (Maxwellian) spectrum of translational energies. For several alkali halides (potassium and rubidium chlorides, bromides, and iodides), however, a significant part of the halogen atoms is ejected with nonthermal energies, i.e. energies of the order of 0.1 eV. The results of recent systematic studies of angular-resolved kinetic energy distributions of the emitted particles will be reported and current views on the electronic mechanisms of desorption will be described. In particular, it will be shown that the ESD mechanism can be understood in terms of the model involving a surface localisation of the so called “hot-holes” created by electron bombardment of alkali halides. A role of hot holes in ESD processes will further be discussed in relation to very recent experimental results obtained for the KBr crystals doped with In impurities which act as efficient hole traps. 相似文献
6.
The electrolytic sensor described is based on the oxidation of nitrite at a platinum electrode modified with chemisorbed iodine and coated with a thin layer of quaternized poly(4-vinylpyridine), qPVP. The sealed sensor uses an anion-exchange membrane to separate Donnan transport of nitrite across the membrane and controlled potential electrolysis at the Pt/qPVP indicator electrode. The sensor has a linear response to nitrate concentration in aqueous samples over the range 4 × 10?6?2 × 10?3 M nitrite. The detection limit is 2 × 10?6 M nitrite. The sensor is free of interference by nitrate, dissolved oxygen, cations, and many neutral species. Anions that are electroactive at 0.7 V vs. Ag/ AgCl would interfere, but they are uncommon in most samples. Initial tests with lake water samples suggest that this sensor is unaffected by this matrix. The system was also evaluated for monitoring nitrite levels in spiked meat extracts. 相似文献
7.
An analytical derivation of multicenter and multiparticle integrals for explicitly correlated Cartesian Gaussian-type cluster functions is demonstrated. The evaluation method is based on the application of raising operators that transform spherical cluster Gaussian functions into Cartesian Gaussian functions. 相似文献
8.
The effects of substituents at C5, C6 and C7 on the solvolysis rates of 2-norbornyl p-toluene sulfonates confirm that through space induction is directional and depends on distance and bridging strain. 相似文献
9.
Local density and generalized gradient approximation time-dependent density functional methods have been used for calculation of the singlet and triplet excited states of nickel-porphine, Ni-tetraphenyloporphine, and Ni-octaethyloporphyrine. Special attention is paid to metal-ligand transitions and d-d transitions. It is shown that the lowest exited singlet states of the three compounds can be described as a transfer of an electron from the porphine ring to the d(x2-y2) orbital of the nickel atom. On the other hand, the lowest excited triplet state arises from promotion of an electron between two nickel d orbitals, an occupied d(z2) and an empty d(x2-y2). It is proposed that a rapid quenching of the excited singlet states is due to an ultrafast intersystem crossing between 1Eg)and 3Eg or 3B1g states. 相似文献
10.
The widespread occurrence of the neutral loss of one to six amino acid residues as neutral fragments from doubly protonated tryptic peptides is documented for 23 peptides with individual sequences. Neutral loss of amino acids from the N-terminus of doubly charged tryptic peptides results in doubly charged y-ions, forming a ladder-like series with the ions [M + 2H](2+) = y(max) (2+), y(max - 1) (2+), y(max - 2) (2+), etc. An internal residue such as histidine, proline, lysine or arginine appears to favor this type of fragmentation, although it was sometimes also observed for peptides without this structure. For doubly protonated non-tryptic peptides with one of these residues at or near the N-terminus, we observed neutral loss from the C-terminus, resulting in a doubly charged b-type ion ladder. The analyses were performed by Q-TOF tandem mass spectrometry, facilitating the recognition of neutral loss ladders by their 2+ charge state and the conversion of the observed mass differences into reliable sequence information. It is shown that the neutral loss of amino acid residues requires low collision offset values, a simple mechanistic explanation based on established fragmentation rules is proposed and the utility of this neutral loss fragmentation pathway as an additional source for dependable peptide sequence information is documented. 相似文献