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排序方式: 共有649条查询结果,搜索用时 31 毫秒
1.
Leila Torkian Mostafa M. Amini Tayebeh Gorji Omid Sadeghi 《Arabian Journal of Chemistry》2019,12(7):1315-1321
In this study, multiwalled carbon nanotube (MWCNT) was modified by the pyridine group using a silane agent and characterized by infrared spectroscopy (IR), thermal analysis (TG/DTA), and elemental analysis (CHN) and scanning electron microscopy (SEM). The application of this sorbent was investigated in determination of lead ions in aqueous samples, using flame atomic absorption spectrometry (FAAS). Through this study, different parameters such as pH and sample flow rate on adsorption process and eluent concentration, volume and flow rate were optimized. The limit of detection (LOD), the relative standard deviation and the recovery of the method were 2 ng mL?1, 1.3% and 99.7%, respectively. Two standard reference materials (NIST 1571 and NIST 1572) were used to verify accuracy of this method. Finally, the sorbent was successfully applied for extraction and determination of low levels of Pb(II) ions in aqueous samples. 相似文献
2.
Khalil Farhadi Ramin Maleki Rouhollah Hosseinzadeh Yamchi Hashem Sharghi Mojtaba Shamsipur 《Analytical sciences》2004,20(5):805-809
[5,10,15,20-Tetrakis(4-N,N-dimethylaminobenzene)porphyrinato]Mn(III) acetate (MnTDPAc) was applied as an ionophore for an iodide-selective PVC membrane electrode. The influences of the membrane composition, pH of the test solution and foreign ions on the electrode performance were investigated. The sensor exhibited not only excellent selectivity to iodide ion compared to Cl- and lipophilic anions such as ClO4- and salicylate, but also a Nernstian response with a slope of -59.4 +/- 1.2 mV per decade for iodide ions over a wide concentration range from 1.0 x 10(-2) to 7.5 x 10(-6) M at 25 degrees C. The potentiometric response was independent of the pH of the solution in the pH range of 2 - 8. The electrode could be used for at least 2 months without any considerable divergence in the potential. Good selectivity for iodide ion, a very short response time, simple preparation and relatively long-term stability were the silent characteristics of this electrode. It was successfully used as an indicator electrode in the potentiometric titration of iodide ions, and also in the determination of iodide from seawater samples and drug formulations. 相似文献
3.
We examine the validity of the application of the Factorization Approximation to derive the Master Equation for a microscopic system coupled to a reservoir. We developed a formal perturbation expansion for the time evolution of the system reduced density matrix. We employed a diagrammatic schemes to produce each term of the perturbation series. The diagrams in the time domain provide a distinct criteria to distinguish the diagrams which survive the Factorization Approximation. The Feynmann-like diagrams in the energy domain, originated from the Resolvent method, are used for execution of diagram summations to estimate their overall contributions. We demonstrated that for a two level atomic system, interacting with a thermal reservoir, the summation over the diagrams which survived the Factorization Approximation, yields the proper time evolution of the system, in agreement with the solution of the Master Equation. The summation of the diagrams which are excluded by applying the Factorization Approximation are characterized by a dimensionless parameter: Γ/ω0, where ω0 is the frequency of the transition line, and Γ is the line width. The Factorization Approximation is thus rigorously justified when this expansion parameter is very small. 相似文献
4.
Latifeh Navidpour Leila Karimi Mohsen Amini Mohssen Vosooghi Abbas Shafiee 《Journal of heterocyclic chemistry》2004,41(2):201-204
Arylation of the readily available 3‐alkythio‐5‐aryl‐1,2,4‐triazoles gave 5‐alkylthio‐1,3‐diaryl‐1,2,4‐triazoles in moderate yield. The structures of the latter were confirmed by NOE and 13C‐NMR. 相似文献
5.
Hassan Sedaira Kamal A. Idriss Elham Y. Hashem Mohamed M. Seleim Abu-Bakr El-Nady 《Journal of solution chemistry》1996,25(1):95-103
The solvation number and hydration constant of Th4+ in ethanol-water medium were determined at 25°C using UV-spectral and electrochemical measurements. A solvate formation equilibrium is demonstrated and characterized. Three molecules of ethanol (S) can bond to the metal cation with strengths comparable to that for H2O to form ThS3(H2O) 3 4+ Formation of thorium monochelate with lawsone (2-hydroxy-1,4-naphthoquinone) eliminates bonding with alcohol molecules. The dissociation constant of the chelating agentsKa and the formation contant of the monochelated metal ionsK f * that are essentially independent of the solution composition are evaluated. Hydration titrations involving thorium-lawsone monochelate are performed and the data obtained from the changes of pH with solvent composition are analyzed. The solution independent constant,sK f * for thorium-lawsone complex formation in mixed aqueous ethanol is given by $$log_s K_f * = vpK_a + log_s K_h - log[LH] - vpH + 3logv$$ where vpKa is the dissociation constant of the chelating agent LH in the solvent system of ν volume fraction of water andsKh is the solution-independent hydration constant of thorium (IV) in the solvent system. Log-values for the constantssKh,sK f * andsK a * are found to be 7.8±0.02, 11.38±0.04 and ?0.753, respectively. 相似文献
6.
The principles for the determination of conditional association constants of enantiomers by capillary zone electrophoresis employing a partial filling technique (PFT) using methyl-beta-cyclodextrin as chiral selector is presented. Orciprenaline was used as a model compound. Partial filling is a separation technique, where different lengths of the chiral selector solution are introduced into the capillary to a final zone length shorter than the effective length of the capillary, prior to application of the solutes. Lengthening of the separation zone results in improving enantioresolution in addition to decreasing electrophoretic mobility of the enantiomers, because of longer interaction time between the solute and chiral selector. The degree of the reduction in electromobility depends on the affinity of the solute to the chiral selector, i.e. strength of the complex formed between the solute and cyclodextrin. The decrease in the electrophoretic mobility with increasing length of the separation zone is used for determination of the association constant. The association constants of the enantiomers of orciprenaline and the chiral selector were evaluated from the slope of the plot, observed electrophoretic mobility versus the ratio between the length of the separation zone and the effective length of the capillary. It was found that the association constants were independent of the chiral selector concentration. The mean values were 110 M(-1) and 160 M(-1) for respective enantiomer. Constants obtained by a conventional CE technique were in good agreement with those from the PFT experiments. The highest enantioselectivityy was obtained when about 50% of the solute was distributed to the selector phase. 相似文献
7.
Spectrophotometric studies have been made to investigate the reaction of Nickel and Lead with 2-carboxy-2'-hydroxy-5'-sulfoformazyl-benzene (zincon) in 50%(v/v) ethanol-water at 25 degrees C and an ionic strength of 0.1 M NaClO4. A complete picture of the complexation equilibria in the pH range (4.2-12.0) for nickel and (1.9-11.5) for lead are presented. Simple, rapid, selective and sensitive methods for the spectro-photometric determination of nickel and lead has been developed based on the color reaction of their complexes with zincon. The methods allow the determination of 4.69 microg mL(-1) of nickel at pH = 6.3 (lambdamax = 665 nm) and 10.3 microg ml(-1) of lead at pH = 5.6 (lambdamax = 610 nm). The apparent molar absorptivities were epsilon = 1.3 x 10(4) L mol(-1) cm(-1) for nickel and epsilon = 0.6 x 10(4) L mol(-1) cm(-1) for lead. The interference of a large number of foreign ions and complexing agents has been studied. Thiosulphate, as masking agent allows the simultaneous determination of nickel and lead in the presence of high concentrations of copper. Ascorbic acid, sodium cyanide and or sodium fluoride provide the elimination of many other interferences. The methods have been applied successfully to the simultaneous determination of nickel and lead in an aluminium and non-ferrous alloy. 相似文献
8.
Bahram Hemmateenejad Hashem Sharghi Morteza Akhond Mojtaba Shamsipur 《Journal of solution chemistry》2003,32(3):215-226
The influence of solvent properties on acidity constants of some newly synthesized 9,10-anthraquinone and 9-anthrone derivatives was studied in methanol-water mixtures in a composition range of 0.57 to 1.0 methanol mole fraction. The model was established by using both multiple linear regression and target factor analysis. Both methods revealed that the solvent polarity/polarizability parameter * is a major factor in controlling the acidity behavior of the anthraquinones and anthrones studied in binary methanol-water mixed solvents. A QSPR study was conducted to drive the relationships between the * coefficient s and the polarity/polarizability of molecules. Both dipole moment and polarizability were found to have a linear relationship with s. The results confirm that, in the dipolar protic solvents used, the dipole-dipole interaction (for neutral molecules) and the ion-dipole interaction (for ionized molecules) are the major factors controlling the acidity behavior of these compounds. 相似文献
9.
Mostafa M. Amini Amirreza Azadmher Hamid Reza Bijanzadeh Nasser Hadipour 《Journal of inclusion phenomena and macrocyclic chemistry》2006,54(1-2):77-80
Behavior of {[(CH3)2SnCl2·H2O]2·18-crown-6}n in solution have been investigated by HMBC NMR. The results show that coordination of water to tin containing species and
its hydrogen bonding to crown ether remains intact in non-coordinating solvent in contrast to coordinating solvent. H-NMR
reveals that the chemical shift of water in complex varies by solvent of crystallization. 相似文献