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31.
H. A. Ergül S. Topcuo?lu E. Ölmez Ç. K?rbaşo?lu 《Journal of Radioanalytical and Nuclear Chemistry》2006,268(1):133-136
Summary Radionuclide (137Cs, 238U, 232Th and 40K) concentrations were determined in a sediment trap and bottom sediment samples collected from a station at the eastern Turkish
coast of the Black Sea. The specific activity of the 137Cs radionuclide in the settling particles ranged from 0.04±0.01 to 0.10±0.02 Bq. g-1dry weight. The calculated flux rate of the 137Cs was between 0.37 and 2.59 Bq. m-2. d-1in the sampling periods of 2002 and 2003. The 137Cs concentration in the bottom sediment profile were between 0.039±0.013-9.083±0.017 Bq. g-1dry weight in the same station. The vertical profile of the radionuclides suggests that they have little mobility during the
17 years after the Chernobyl accident. 相似文献
32.
Kai‐lu Yu Chang‐jun Liu Yue‐ping Zhang Fei He Xin‐li Zhu Baldur Eliasson 《Plasma Chemistry and Plasma Processing》2004,24(3):393-403
PdO/Al2O3 catalysts prepared by glow discharge plasma treatment followed by thermal calcination show a much higher dispersion and a better catalytic activity for methane combustion at relatively low temperatures. The dispersion of palladium active species by such plasma prepared catalysts is 29.7%, 5.4 times higher than that of conventional catalysts. XPS analysis indicates that a surface enrichment of Pd active species (PdO) has been achieved after plasma treatment. The surface atomic composition of PdO of plasma prepared catalysts reaches 10.5%. XRD characterization also confirms a wellcrystallized PdO phase present on the plasma prepared catalyst. The lightoff temperature of the plasma prepared catalyst is 370°C, 50°C lower than that obtained from the conventional catalyst. 相似文献
33.
The binary and mixed-ligand complexes formed between ligands (histidine (His), histamine (Him) and glycine (Gly)) and some transition metals (Cu(II), Ni(II) and Zn(II)) were studied potentiometrically in aqueous solution at (25.0 ± 0.1) C and I = 0.10 M KCl in order to determine the protonation constants of the free ligands and stability constants of binary and ternary complexes. The complexation model for each system has been established by the software program BEST from the potentiometric data. The most probable binding mode for each binary species of histidine and for all mixed species was also discussed based upon derived equilibrium constants and stability constants related to the binary species. The ambidentate nature of the histidine ligand, i.e. the ability to coordinate histamine-like, imidazolepropionic acid-like and glycine-like modes was indicated from the results obtained. The stability of ternary complexes was quantitatively compared with their corresponding binary complexes in terms of the parameters, log K, log X and 1110. The concentration distributions of various species formed in solution were also evaluated. In terms of the nature of metal ion, the complex stability follows the trend Cu(II) > Ni(II) > Zn(II), which is in agreement with the Irving-Williams order of metal ions. Thus, the results obtained were compared and evaluated with those in the literature. 相似文献
34.
Removal of methyl violet from aqueous solution by perlite 总被引:2,自引:0,他引:2
The use of perlite for the removal of methyl violet from aqueous solutions at different concentration, pH, and temperature has been investigated. Adsorption equilibrium is reached within 1 h. The capacity of perlite samples for the adsorption of methyl violet was found to increase with increasing pH and temperature and decrease with expansion and increasing acid-activation. The adsorption isotherms are described by means of the Langmuir and Freundlich isotherms. The adsorption isotherm was measured experimentally at different conditions and the experimental data were correlated reasonably well by the adsorption isotherm of Langmuir. The order of heat of adsorption corresponds to a physical reaction. It is concluded that the methyl violet is physically adsorbed onto the perlite. The removal efficiency (P) and dimensionless separation factor (R) have shown that perlite can be used for removal of methyl violet from aqueous solutions, but unexpanded perlite is more effective. 相似文献
35.
Duygu Avci Selim H. Kseflu Robert D. Thompson Lon J. Mathias 《Journal of polymer science. Part A, Polymer chemistry》1994,32(15):2937-2945
New ester derivatives of ethyl α-hydroxymethylacrylate were synthesized using acid chlorides (traditional solution reactions), sodium salts of acids (with phase transfer catalysis), and trifluoroacetic anhydride (trifluoroacetate). The interfacial process gave high yields of clean products under very mild conditions. Derivatives obtained include the formate, acetate, hexanoate, stearate, benzoate, trifluoroacetate, and adamantanoate. Bulk polymerizations with 2,2′-azobis (isobutyronitrile) gave high molecular weight polymers with intrinsic viscosities of over 2 dL/g and molecular weights of several million [based on size-exclusion chromatography (SEC) comparison to polystyrene standards]. These high molecular weights were the result of autoacceleration in the bulk as shown by monitoring molecular weight with respect to conversion. Solution polymerization in benzene gave more typical polymer, e.g., the acetate derivative showed an SEC molecular weight of 52,000. Glass transition temperatures for the n-alkyl esters decreased from the formate (77°C) to the hexanoate (15°C); the stearate showed a side-chain melting point of 40°C but no Tg. Glass transitions were observed for the trifluoroacetate, benzoate, and adamantanoate polymers at 69, 130, and 214°C, respectively. Solution 13C-NMR showed evidence of tacticity information for the formate and acetate derivatives with appaent preference for syndiotactic polymer formation similar to that of methyl methacrylate. FTIR and solid-state 13C-NMR analysis gave spectra with functional group peaks and chemical shift values expected based on composition. The stearate monomer and polymer gave solid-state 13C chemical shifts of 34 and 33 ppm, respectively, for the central CH2 units consistent with monoclinic and orthorhombic crystal packing. © 1994 John Wiley & Sons, Inc. 相似文献
36.
Summary A
tail-made polymer matrix is proposed to remove strontium ions from aqueous
solutions. The removal behavior of strontium ions on a crosslinked copolymer
containing methacrylic acid as functional groups was investigated as a function
of sorptive concentration, time, temperature and pH. It was observed that an
increase of these parameters enhanced the removal of Sr(II) ions from aqueous
solution. It is found that a maximum adsorption of Sr(II) ions can be obtained
on the crosslinked copolymer after 30 minutes and at pH 8. The increase of
Sr(II) ion concentration in the solution resulted in an increase in the amount
of Sr(II) ions adsorbed on the crosslinked copolymer containing methacrylic
acid as functional groups. However, after a maximum of Sr(II) concentration in
the solution, the percentage of adsorbed Sr(II) ions decreased. The adsorption
data are well represented by the Freundlich, Langmuir and Dubinin-Radushkevich
(D-R) isotherms. The adsorption capacity of the copolymer and the free energy
change were calculated by using the D-R isotherm. For the adsorption of Sr(II)
ions on the crosslinked copolymer the thermodynamic parameters (DH°,DS° andDG°) were
calculated.</p>
</p> 相似文献
37.
B. Karakelle N. Öztürk A. Köse A. Varinlioğbrevelu A. Y. Erkol F. Yilmaz 《Journal of Radioanalytical and Nuclear Chemistry》2002,254(3):649-651
The city of Kocaeli is in the western part of Anatolia in Turkey and has a population of approximately 1.000.000. There is no information about radioactivity in the Kocaeli soils samples so far. For this reason, the concentrations of the natural radionuclides in soil samples from 27 different sampling stations in Kocaeli Basin and its surroundings have been determined. The results have been compared with other radioactivity measurements in different country"s soils. The typical concentrations of 137Cs, 238U, 40K, 226Ra, 232Th found in surface soil samples ranged from 2±0.6 to 25±6 Bq/kg, from 11±4 to 49±10 Bq/kg, from 161±30 to 964±127 Bq/kg, from 10±4 to 58±11 Bq/kg, and from 11±3 to 65±13 Bq/kg, respectively. 相似文献
38.
Y. Şahin R. Durak Y. Kurucu S. Erzeneoğlu 《Journal of Radioanalytical and Nuclear Chemistry》1994,177(2):403-413
Two analytical shape functions representing the shapes of - and characteristic X-ray photopeak sides obtained with a Ge(Li) detector are described. The photopeak centroid is accurately determined by using these functions. Energy dependence of photopeak tailing at the lower energy side of the photopeaks are obtained by the least-squares fitting method. The present method can be used for the analysis of partly overlapped photopeaks, one side of which is well resolved, with a sufficient accuracy. 相似文献
39.
A. Baştuğ Ö. Söğüt Y. Şahin M. Ertuğrul 《Journal of Radioanalytical and Nuclear Chemistry》2002,251(2):323-327
La and Lb X-ray fluorescence cross sections in Er, Ta, W and Au at excitation energies of 16.896, 22.581, 25.770, 32.890, 38.184, 43.949, 50.214 and 59.5 keV were investigated. Measurements were made using a low energy Si(Li) detector coupled to a model 4096 computerized multi-channel analyser. The experimental results were compared with the theoretically calculated values of L X-rays fluorescence cross sections and other experimental results. Good agreement was observed between experimental and theoretical values. 相似文献
40.
G. Erdogduğ 《Journal of Analytical Chemistry》2002,57(7):620-623
A gold electrode was modified with electropolymerized films of 4-methoxyphenol by its oxidative polymerization from an alkaline solution by cyclic voltammetry. The modified electrode was then used to determine epinephrine (EP) in the presence of a high concentration of ascorbic acid (AA) by differential pulse voltammetry. The peak positions as well as relative sensitivity EP/AA were affected by the potential window used for the polymerization. For polymerization between 0 and 1.3 V, the peak potentials recorded in a phosphate buffer solution (pH = 7.2) were 516 and 312 mV vs. Ag/AgCl for EP and AA, respectively. In addition the effects of pH and the type of electrolyte on the linearity range and detection limit are investigated. The detection limit for 3s-test is 0.1 M. The high selectivity and sensitivity for epinephrine was found to be due to charge discrimination/analyte accumulation. 相似文献