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91.
Spectrophotometric Determination of Thorium with Disodium Salt of Arsenazo-III in Perchloric Acid 总被引:1,自引:0,他引:1
M. Haleem Khan A. Ali N. Niaz Khan 《Journal of Radioanalytical and Nuclear Chemistry》2001,250(2):353-357
A rapid and sensitive spectrophotometric method has been developed for the determination of thorium using 0.04% Arsenazo-III in a 2M perchloric acid solution. Absorbance was measured in 1 cm cell and the complex has a sensitive absorption peak at 654 nm. The complex is formed instantly in perchloric acid and remains stable for 45 minutes with constant absorbance. Beer's law is obeyed in the range 1–60 g·g–1 of thorium concentration with a molar absorptivity at 654 nm = 3.07·105 M–1·cm–1 at 24±2°C. The foreign ions interference in thorium determination have been checked. The cations were tested at >60-fold excess of thorium, Mn(II), Fe(III), Co(II) and Ni(II) interfere negatively, whereas only Ce(III) has increased the absorbance. Among the anions, cyanide, phosphate, thiocyanate and acetate at 150-fold excess of thorium cause significant interference. However, thorium can bedetermined in the presence of nitrate, chloride, oxalate, tartrate, ascorbate, thiosulphate and citrate. The method has been applied on certified reference material for thorium determination after extractive separation and the result was found in good agreement with the certified value. The method has been also applied successfully to determine thorium at g·g–1 level in local ore samples with a precision of ±0.04%. 相似文献
92.
Nizakat Bib Misal Khan Amal Badshah Muhammad Ashraf Chaudry 《Radiation Physics and Chemistry》2005,73(6):362-364
Minimally processed cauliflower samples were irradiated, stored at 5 °C for 2 weeks and analyzed for sensory, physicochemical and microbiological qualities at 0th, 7th and 14th days. The data showed highest mean values of 7.93 and 7.57 for appearance and flavor, respectively, for 1.0 kGy treated samples. The D10 values of contaminating microorganisms on cauliflower were 0.20 (Escherischia coli) and 0.24 kGy (Salmonella paratyphae A.) and the resulting 5D10 value was 1.2 kGy. The study revealed that a dose of 1.5 kGy is enough for retention of quality and reduction of microbial load to 5D10 values in cauliflower during 2 weeks storage at refrigerated temperature. 相似文献
93.
Garraffo HM Spande TF Jain P Kaneko T Jones TH Blum MS Ali TM Snelling RR Isbell LA Robertson HG Daly JW 《Rapid communications in mass spectrometry : RCM》2001,15(16):1409-1415
Chemical ionization tandem mass spectrometry (CI-MS/MS) of alkaloids with ammonia reagent gas and collision-activated dissociation as well as EI-MS/MS were applied to the tetraponerine alkaloids in extracts from six pseudomyrmecine ants of the genus Tetraponera. The MS/MS techniques along with gas chromatography Fourier transform infrared (GC/FTIR) spectra allowed identification in two extracts of seven of the eight known tetraponerines. The EI-MS/MS fragmentations proved diagnostic for the ring system and the CI-MS/MS patterns for the C-8 or C-9 substitution, while the Bohlmann bands in FTIR spectra were diagnostic for the C-8 or C-9 configurations. An Indian ant (T. allaborans) had T-2, T-4 and T-8, while a Chinese ant (T. binghami) had T-5, T-6, T-7 and T-8. Four other ants, T. rufonigra (India), T. penzigi (Africa), T. clypeata (Africa) and T. sp. cf. emeryi (Africa), had no tetraponerines. 相似文献
94.
Zahid H. Khan 《International journal of quantum chemistry》1992,42(6):1717-1735
Electronic transition energies of radical cations of 1.2-, 1.3-, 1.6-, and 1.7?dihydroxynaphthalenes are calculated using an open-shell SCF method with configuration interaction. The results are critically analyzed and a correlation diagram is given that shows the energy-shift and intensity variation in the electronic transitions when moving from one system to another, thus revealing the characteristic behavior of the transitions depending on the positions of the hydroxyl substituents. An interesting relation connecting the electronic spectroscopy with the UV photoelectron spectroscopy is suggested on the basis of which the first ionization potentials (IPS ) of the substituted aromatic systems can be inferred from the calculated energy of the A-type (HOMO → LUMO ) transitions for their radical cations. Furthermore, the predictability of the IP s is found to be considerably increased with the incorporation of “molecular size” in the regression. 相似文献
95.
Effects of relative humidity conditions in the irradiation chamber and of temperature of the chamber on the response of 3 mm thick light blue poly (methyl methacrylate) sheets have been studied. The response was measured spectrophotometrically at 402, 450, 596 and 612 nm. The response of the dosimeter is independent of the relative humidity (12–97%) during irradiation if the response is measured within 24 h of irradiation. If the response is measured after longer storage time, the absorbance at 402 and 450 nm increases significantly. At these two wavelengths the response of the dosimeter is also independent of the temperature of the irradiation chamber in the range of 0 to 40 °C. However, at higher temperatures (60, 80 °C), the response is not uniform. 相似文献
96.
Sonia Jam Masume Ghalbi Ahangary Ahmad Tavasoli Kambiz Sadaghiani Ali Nakhaei Pour 《Reaction Kinetics and Catalysis Letters》2006,89(1):71-79
Summary An integrated process for producing liquid fuels from synthesis gas via a two-stage Fischer-Tropsch (FT) reaction is disclosed. An iron catalyst was used in the first bed of a fixed-bed reactor
followed by a ruthenium promoted cobalt catalyst in the second bed. The activity and selectivity of the dual-bed system were
assessed and compared with those using catalysts in a single bed system, separately. The methane selectivity in the dual-bed
reactor was about 11% less compared to that of the single-bed system. The C5+ selectivity for the dual-bed reactor was 19.7% higher than that of the single-bed system. 相似文献
97.
In a weakly acidic solution, the addition of HBr to 1-phenylprop-1-yne produces predominantly the anti-Markovnikov product. In this paper, we consider five possible explanations for this behavior and conclude that the concerted addition is occurring on the acetylenic pi bond orthogonal to the extended aromatic pi system. The electronic effect of the distal methyl group and the steric hindrance of the coplanar phenyl ring combine to promote bromide attack at the beta carbon. Attack on this pi bond is insensitive to the electronic effect of meta and para substituents on the ring but is very (sterically) sensitive toward all ortho substituents. 相似文献
98.
Sayed Ali Naghi Taheri R. Alan Jones Santokh Singh Badesha Majed M. Hania 《Tetrahedron》1989,45(24):7717-7728
3,4-Diformyl-2,5-dimethylpyrrole (1) reacts with ,ω-diamino-alkanes, NH2(CH2)nNH2t' to form either the potentially tautomeric 2:2 macrocyclic adduct (7a) (8), when N = 2, or the potentially tautomeric 1:1 bicyclic adduct (18) (19), when N = 4, 5, 6, and 12. 1H and 13C N.m.r. spectral data indicate that the 2-azafulvene structures predominate for both types of cycloadducts. Only polymeric material was obtained when N = 3. 相似文献
99.
Relative rates of solvolysis of some N-triorganosilylanilines in mixtures of ethanol and aqueous potassium hydroxide have been determined, with results as follows. (i) For XC6H4NHSiEt3 compounds in MeOH (5 vol) + aq. alkali (2 vol) at 50°: (X =) H, 1.0;p-Me, 0.80;p-OMe, 0.83;m-Me, 0.90; o-Me, 0.87; p-SMe, 1.90; p-F, 1.7; p-Cl, 2.8; o-Cl, 14; m-Cl, 4.2; m-NO2, 18; p-CN, ca. 43; p-NO2, ca. 120. (ii) For PhNHSi(C6H4Y)3 compounds in MeOH (10 vol) + aq. alkali (1 vol) at 50°: (Y =) H, 1.0; p-OMe, 0.12; p-Cl, ca. 32; m-Cl, ca. 84. (iii) For PhNHSiR3 compounds in MeOH (5 vol) + aq. alkali (2 vol) : (R3 =) Et3, 1.0; Et2Me, 18 (at 30°); Me2-i-Pr, 8 (at 30°);Me2-t-Bu, 0.012 (at 50°);i-Pr3, 0.006 (at 50°). In series (i) the relative rates correlate with σ, or where appropriate σ?-constants, with a ? value of 1.6. It is suggested that in the transition state of the rate-determining step the OSi bond is fully formed, or almost so, the SiN bond approximately 20—50% broken, and the bond between the nitrogen atom and a proton from the solvent ca. 10—30% formed. 相似文献
100.
Structural characterization of nanosized CeO(2)-SiO(2), CeO(2)-TiO(2), and CeO(2)-ZrO(2) catalysts by XRD, Raman, and HREM techniques 总被引:1,自引:0,他引:1
Reddy BM Khan A Lakshmanan P Aouine M Loridant S Volta JC 《The journal of physical chemistry. B》2005,109(8):3355-3363
Structural characteristics of nanosized ceria-silica, ceria-titania, and ceria-zirconia mixed oxide catalysts have been investigated using X-ray diffraction (XRD), Raman spectroscopy, BET surface area, thermogravimetry, and high-resolution transmission electron microscopy (HREM). The effect of support oxides on the crystal modification of ceria cubic lattice was mainly focused. The investigated oxides were obtained by soft chemical routes with ultrahighly dilute solutions and were subjected to thermal treatments from 773 to 1073 K. The XRD results suggest that the CeO(2)-SiO(2) sample primarily consists of nanocrystalline CeO(2) on the amorphous SiO(2) surface. Both crystalline CeO(2) and TiO(2) anatase phases were noted in the case of CeO(2)-TiO(2) sample. Formation of cubic Ce(0.75)Zr(0.25)O(2) and Ce(0.6)Zr(0.4)O(2) (at 1073 K) were observed in the case of the CeO(2)-ZrO(2) sample. Raman measurements disclose the fluorite structure of ceria and the presence of oxygen vacancies/Ce(3+). The HREM results reveal well-dispersed CeO(2) nanocrystals over the amorphous SiO(2) matrix in the cases of CeO(2)-SiO(2), isolated CeO(2), and TiO(2) (anatase) nanocrystals, some overlapping regions in the case of CeO(2)-TiO(2), and nanosized CeO(2) and Ce-Zr oxides in the case of CeO(2)-ZrO(2) sample. The exact structural features of these crystals as determined by digital diffraction analysis of HREM experimental images reveal that the CeO(2) is mainly in cubic fluorite geometry. The oxygen storage capacity (OSC) as determined by thermogravimetry reveals that the OSC of the mixed oxide systems is more than that of pure CeO(2) and is system dependent. 相似文献