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81.
An analytical scheme is proposed which combines three speciation techniques for determination of particular Al species in soil extracts and percolating waters. A cation-exchange fast protein liquid chromatography — inductively coupled plasma atomic emission spectrometry (FPLC-ICP-AES) procedure, a microcolumn chelating ion-exchange chromatography- atomic absorption spectrometry (MCC-ETAAS) technique and the 8-hydroxyquinoline spectrophotometric method (8HQ-spectrophotometry) were employed. The FPLC-ICP-AES procedure offers determination of Al3+ (retention time 4.5 min) and Al(OH)2+ species (retention time 4.0 min) which are separated from Al(OH)+
2 (retention time 1.5min). AlF2+ coelutes with Al(OH)2+ species, while Al(SO4)+, AlF+
2 and negatively charged Al organic complexes coelute with Al(OH)+
2 species. The MCC-ETAAS technique enables determination of the sum of positively charged monomeric aqua- and hydroxy-Al species plus sulphate- and fluoro-Al complexes. Employing the 8HQ-spectrophotometry the sum of positively charged monomeric aqua- and hydroxy-Al species plus sulphato- and most of the labile organic Al species are determined. The sensitivities of these selected techniques were adequate for speciation of Al in the samples analyzed. On the basis of the specific selectivity of a particular technique various groups of Al species may be determined. Thus, the comparison of analytical data from complementary procedures provides more comprehensive information on Al species present in soil extracts and percolating waters. 相似文献
82.
Lucifer yellow and lissamine rhodamine sulfonyl hydrazine were used as the donor and the receptor, respectively, for Förster energy transfer measurements to determine the location of the subunit in the native Na,K-ATPase from pig kidney. It was found that (1) the subunits are located in one functional complex, i.e., the dimer ()2 appears to be the functional complex of Na,K-ATPase, and (2) the subunits in the functional enzyme complex in the membrane are not located next to each other but are rather well separated. The distance between fluorophores covalently attached to the subunits was found to be 5.3 nm. 相似文献
83.
V. S̆unjić M. Oklobdžija A. Lisini A. Sega F. Kajfez D. Srzić L. Klasinc 《Tetrahedron》1979,35(21):2531-2537
The rate for degenerate nucleophilic exchange (ke) of the C(3)-OH group in the racemic compound 1 was determined in DMSO/H218O using mass spectrometry. Epimerization rates for diastereomers 15 and 16 were determined by polarimetry (kep) and NMR spectroscopy (kr-c—for ing-hain tautomery). The ratio ~ 3.5 35° is close to that obtained for degenerate nucleophilic exchange of the C(3)-OMe group in the compound 1a ( ~4, Refs. [3,4]). These data confirm the C(3)-OH substituted 1,4-benzodiazepin-2-ones lose the configurational identity of the C(3) chiral centre by both direct nucleophilic substitution of the OH group, and ring-chain tautomery processes.The synthesis of the diastereomeric compounds 15 and 16, and their chromatographic separation is described. 相似文献
84.
Jiří Kohout Mária Kabešová Prof. Dipl.-Ing. Dr. Ján Gažo 《Monatshefte für Chemie / Chemical Monthly》1977,108(5):1011-1018
The infrared spectra of thiocyanato-copper(II) complexes of the type Cu(NCS)2
L
2 with all isomeric picolines and lutidines (L) as well as those of the type Cu(NCS)2
L
3 withL=3- and 4-picoline, 3,4- and 3,5-lutidine were measured. The behaviour of the (CN) stretching vibrations of the Cu(NCS)2
L
2 complexes led to conclusions on the different kind of coordination of the NCS groups in dependence on the ligandL. The mutually conditioned strength of the Cu–NCS and Cu–N(L) bonds in the equatorial plane, especially in the presence of ligandsL with the steric effect, was determined from the frequency shift of the Cu–NCS and Cu–N(L) stretching vibrations with regard to the vibrations for Cu(NCS)2(pyridine)2.
Mit 1 Abbildung 相似文献
Mit 1 Abbildung 相似文献
85.
The extraction of Am, Eu, Ce(III), Zr(IV), and Sr from aqueous nitric acid— nitrate media by dibutyl N,N-diethylcarbamylphosphonate
and dibutyl N,N-diethylcar-bamylmethylenephosphonate dissolved in carbon tetrachloride was studied. The trivalent actinide
and lanthanide elements may be separated in certain aqueous phase acidity regions from Fe(III), Zr(IV), and Sr, whereas the
separation of actinide elements from the lanthanide elements is poor. The extractant to metal ratio in the extracted complexes
of Am, Eu, and Ce(III) is 3. The interferences in the extraction due to acidic impurities in the extracting agent are discussed. 相似文献
86.
R.R. Adžić D.N. Simić A.R. Despić D.M. Dražić 《Journal of Electroanalytical Chemistry》1977,80(1):81-99
The catalytic effects of a submonolayer of lead on noble metals have been shown and discussed in terms of a previously published model. A theoretical analysis of these effects is presented. It was demonstrated that foreign metal monolayers allow a determination of the true catalytic activity of electrodes in the case of self-poisoning reactions. A volcano-shaped curve for oxidation of formic acid on noble metal electrodes was obtained. 相似文献
87.
A correction method is proposed for the quantitative determination of stoichiometric ratios in porous materials by electron microprobe analysis. Analysis of this kind of material is complicated by an imperfect surface that can only be improved to some extent. The correction is based on a linear dependence (different for each element) of the analyses on a sum of weight concentrations of oxides. With this correction it is possible to use analyses affected by the imperfection of the surface with much better confidence compared to common normalisation. An example is presented for a series of ceramic superconductors Bi2.1(SrCa)2.9Cu2O8+. 相似文献
88.
M. Ježabek J. Karczmarczuk M. Rożańska 《Zeitschrift fur Physik C Particles and Fields》1985,29(1):55-60
In the framework of the dual parton model we calculate the spectra of secondary antibaryons in \(\bar p\) -nucleus non-annihilation inelastic interactions. We find that the number of antibaryons in the backward hemisphere in the \(\bar p\) -nucleon centre-of-mass frame can grow with the atomic number of the nucleus. 相似文献
89.
J. Kohout M. Quastlerová-Hvastijová J. Gažo 《Monatshefte für Chemie / Chemical Monthly》1973,104(3):779-783
Zusammenfassung Die Ligandenfeldspektren der Komplexe des Typs Cu(NCO)2
L
2 (L=Ligand der Chinolin- bzw. Isochinolingruppe) im festen Zustand wurden aufgenommen. Das Spektrum des Komplexes Cu(NCO)2(Chin)2 weist eine einzige Bande auf und deutet auf eine pseudooktaedrische Struktur. Die Spektren der übrigen Komplexe enthalten hingegen neben den Hauptbanden auch Schultern bzw. ist die anwesende Bande zusammengesetzt, so daß diese Spektren mit einer planaren Struktur im Einklang sind. Die annähernden Werte für den Parameter 10Dq wurden berechnet; sie liegen im Bereich von 7,1 bis 7,8 kK.
Mit 1 Abbildung
6. Mitt.:M. Quastlerová-Hvastijová, J. Kohout undJ. Gao, Z. anorg. allgem. Chem., im Druck. 相似文献
Ligand field spectra of some cyanato-copper(II) complexes with ligands from the quinoline- and isoquinoline group
The ligand field spectra of complexes of the type Cu(NCO)2 L 2 (L=ligand from the quinoline or isoquinoline group) in the solid state were recorded. Only the spectrum of Cu(NCO)2(Quin)2 exhibits a single band and indicates a pseudooctahedral structure, while the spectra of the remaining complexes also contain shoulders in addition to the main band, or this band is composite, thus being in accordance with a planar structure. The approximate values of the parameter 10Dq were calculated and found to be in the range of 7.1 to 7.8 kK.
Mit 1 Abbildung
6. Mitt.:M. Quastlerová-Hvastijová, J. Kohout undJ. Gao, Z. anorg. allgem. Chem., im Druck. 相似文献
90.
Silva Silvio S. Ribeiro JoÃo D. Felipe Maria G. A. Vitolo Michelle 《Applied biochemistry and biotechnology》1997,(1):557-564
Batch fermentations of sugar cane bagasse hemicellulosic hydrolysate treated for removing the inhibitors of the fermentation
were performed byCandida guilliermondii FTI20037 for xylitol production. The fermentative parameters agitation and aeration rate were studied aiming the maximization
of xylitol production from this agroindustrial residue. The maximal xylitol volumetric productivity (0.87 g/L h) and yield
(0.67 g/g) were attained at 400/min and 0.45 v.v.m. (KLa 27/h). According to the results, a suitable control of the oxygen input permitting the xylitol formation from sugar cane
bagasse hydrolysate is required for the development of an efficient fermentation process for large-scale applications. 相似文献