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71.
Mojtaba Shamsipur Hamid Reza Rajabi Mohammad Hassan Beyzavi Hashem Sharghi 《Mikrochimica acta》2013,180(9-10):791-799
We report on the synthesis of polymeric nanoparticles (PNPs) containing a tetrakis(3-hydroxyphenyl)porphyrin, and their use for the separation of mercury(II) ion. The PNPs were prepared by bulk polymerization from methacrylic acid (the monomer), ethyleneglycol dimethacrylate (the cross-linker), 2,2′-azobisisobutyronitrile (the radical initiator) and the mercury(II) complex of 5,10,15,20-tetrakis(3-hydroxyphenyl)-porphyrin. The Hg(II) ion was then removed by treatment with dilute hydrochloric acid. The PNPs were characterized by colorimetry, FT-IR spectroscopy, and scanning electron microscopy. The material is capable of binding Hg(II) from analyte samples. Bound Hg(II) ions can be eluted with dilute nitric acid and then quantified by cold vapor AAS. The extraction efficiency, the effects of pH, preconcentration and leaching times, sample volume, and of the nature, concentration and volume of eluent were investigated. The maximum adsorption capacity of the PNPs is 249 mg g?1, the relative standard deviation of the AAS assay is 2.2 %, and the limit of detection (3σ) is 8 ng.L?1. The nanoparticles exhibit excellent selectivity for Hg(II) ion over other metal ions and were successfully applied to the selective extraction and determination of Hg(II) ion in spiked water samples. Figure
Schematic presentation of leaching process of mercury(II) ion from the prepared IIP 相似文献
72.
Batch equilibrium studies were conducted at 20 ± 0.5 °C with indigenously synthesized spherical resorcinol–formaldehyde resin beads, using radioanalytical technique, to determine their capacity for sorption of cesium ions from alkaline medium. Equilibrium isotherm studies were carried out, by varying the initial concentrations of cesium from 0.1 to 50 mM. The liquid-to-solid phase ratio of ~100 ml:1 g was maintained for all the sorption experiments. The equilibrium data were fitted to Langmuir and Freundlich isotherm models. It was observed that Freundlich isotherm explains sorption process nicely. The effect of resin size on percentage cesium ion uptake was also investigated, and 20–40 mesh size was found to be the optimum particle size. The cesium sorption capacity of the beads was determined to be ~238 mg/g. The kinetics of the sorption was studied at different initial cesium ion concentrations, and the kinetics data were fitted into various kinetics models. The kinetics of the cesium ion sorption was found to be pseudo second-order. The mechanistic steps involved were found to be complex, consisting of both film diffusion and intraparticle diffusion with film diffusion as the rate limiting step. 相似文献
73.
F. Ditrói F. Tárkányi S. Takács A. Hermanne H. Yamazaki M. Baba A. Mohammadi 《Journal of Radioanalytical and Nuclear Chemistry》2013,298(2):853-865
As a part of our series of studies on charged particle induced reactions on various target materials, proton induced excitation functions on natural cobalt have been determined by using the stacked-foil technique. In these measurements the radionuclides 55,56,57,58Co, 51Cr, 52,54,56Mn and 56,57Ni have been identified. For the above mentioned nuclides the cross-sections were derived from the measured activities and were compared with the literature data and with the results of EMPIRE code calculations and tabulated values in the TENDL 2011 library (based on TALYS code calculations). The agreement with previous measurements and with theoretical values was acceptable. 相似文献
74.
Three diamine monomers with different derivatives of imidazole heterocyclic ring and meta-linked aryl ethers were synthesized and used in polycodensation reaction with various commercial dianhydrides for preparation of a series of novel poly(ether-imide) (PEI)s. The polycodensation reactions were carried out by using conventional method and in a green medium of ionic liquid (IL) without using NMP-pyridine-acetic anhydride. The PEIs were obtained in good yields (80% 96%) with moderate viscosity (0.48 0.66 dL/g) in a shorter reaction time (10 h) in IL as compared with the conventional method (36 h). All of the polymers were amorphous in nature, showed excellent solubility in amide-type polar aprotic solvents with ability to form tough and flexible films, and excellent thermal stability with Tgs in the range of 212 340 ℃ and 10% weight loss temperature (T10) up to 570℃ in N 2 and 528 ℃ in air. 相似文献
75.
Marzieh Mohammadi Akram Zamani Keikhosro Karimi 《Applied biochemistry and biotechnology》2013,171(6):1465-1472
In this study, the effect of phosphorous compound concentration on the production of glucosamine by Mucor indicus was investigated. Changes in the yield of ethanol, the major metabolite of the fungus, were also followed besides. The alkali insoluble material of the biomass of the fungus mainly contained phosphates and polymers of glucosamine and N-acetyl glucosamine, i.e., chitin and chitosan. Yields of glucosamine (78–113 g/kg dry fungal biomass) and ethanol (200–370 g/kg glucose) were significantly affected by the phosphorous concentration. The results showed that lower concentrations of phosphorous favored the production of glucosamine while higher ethanol as well as biomass yields was obtained at higher concentrations. The best concentration was 0.5 g/l where glucosamine yield was 0.37 g/l (11 % of the biomass). At this phosphate concentration, ethanol and biomass yields were 360 and 76 g/kg glucose, respectively. On average, proteins comprised 51.5 % of the biomass. Glycerol was the second important metabolite during the fermentation by the fungus which appeared at lower yields (20–34 g/kg glucose). 相似文献
76.
Pezhman Kazemi Mohammad Peydayesh Alireza Bandegi Toraj Mohammadi Omid Bakhtiari 《Chemical Papers》2013,67(7):722-729
An experimental study on the pertraction of methylene blue (MB) through a supported liquid membrane (SLM) using a mixture of mono-(2-etylhexyl) ester of phosphoric acid (M2EHPA) and bis-(2-etylhexyl) ester of phosphoric acid (D2EHPA) and sesame oil as the liquid membrane (LM) was performed. Parameters affecting the pertraction of MB such as initial MB concentration, carrier concentration, feed phase pH, and stripping phase concentration were analyzed. Optimal experimental conditions for MB pertraction (permeability of 5.63 × 10?6) were obtained after a 7 h separation with the MB concentration in the feed phase of 80 mg L?1, D2EHPA/M2EHPA concentration in membrane phase of 40 vol. %, feed pH of 6, and acetic acid concentration in the stripping phase of 0.4 mol L?1. Kinetics of transport and stability of the SLM system were also studied and the mass transfer coefficient for this system was evaluated. Scanning electron microscopy (SEM) was used to morphologically characterize the membrane surface. 相似文献
77.
The Heck coupling of haloarenes with various alkenes was successfully performed in the presence of 0.5 mole % Pd(OAc)2 and 1.0 mole % d-glucosamine as an additive with K2CO3 as the optimal base in a mixture of H2O/iPrOH (φ r = 2: 1) as the reaction solvent at 80°C after 6 h. d-Glucosamine was found to be an inexpensive, air-stable, easy to available, and efficient additive in palladium-catalyzed Heck reactions of aryl iodides (67–95 % conversion) and bromides (38–72 % conversion). 相似文献
78.
The low temperature perovskite-type calcium titanate (CaTiO3) thin films and powders with nanocrystalline and mesoporous structure were prepared by a straightforward particulate sol–gel route. The prepared sol had a narrow particle size distribution about 17 nm. X-ray diffraction and Fourier transform infrared spectroscopy revealed that, the synthesized powders had highly pure and crystallized CaTiO3 structure with preferable orientation growth along (1 2 1) direction at 400–800 °C. The activation energy of crystal growth was calculated 5.73 kJ/mol. Furthermore, transmission electron microscope images showed that the average crystallite size of the powders annealed at 400 °C was around 3.5 nm. Field emission scanning electron microscope analysis and atomic force microscope images revealed that, the deposited thin films had uniform, mesoporous and nanocrystalline structure with the average grain size in the range 33–39 nm depending on annealing temperature. Based on Brunauer–Emmett–Teller (BET) analysis, the synthesized powders showed mesoporous structure with BET surface area in the range 51–21 m2/g at 400–800 °C. One of the smallest crystallite size and one of the highest surface areas reported in the literature is obtained which can be used in many applications, such as photocatalysts. 相似文献
79.
Mojtaba Amini Mina Bigdeli Sepideh Delsouz‐Hafshejani Arkady Ellern L. Keith Woo 《无机化学与普通化学杂志》2014,640(2):385-389
The reactions of FeCl3 · 6H2O and 2‐(2′‐hydroxyphenyl)‐2‐thiazoline as a bidentate O‐N donor thiazoline ligand (thoz) afford a five‐coordinate FeIII complex [Fe(thoz)2Cl] with a distorted square pyramidal configuration. Complex [Fe(thoz)2Cl] was isolated as air‐stable crystalline solids and fully characterized, including by single‐crystal X‐ray structure analysis. Complex [Fe(thoz)2Cl] shows very efficient reactivity in the oxidation of sulfides to their corresponding sulfoxides using urea hydrogen peroxide (UHP) as the oxidant at room temperature in air. 相似文献
80.
Ghodsi Mohammadi Ziarani Sakineh Faramarzi Negar Lashgari Alireza Badiei 《Journal of the Iranian Chemical Society》2014,11(3):701-709
Sulfonic acid functionalized SBA-15 (SBA-Pr-SO3H) as a new nanoporous solid acid catalyst was applied in the green one-pot synthesis of spiro[indole-tetrahydropyrano(2,3-d)pyrimidine] derivatives via three-component reaction of isatins, malononitrile or cyanoacetic esters and barbituric acids under solvent-free conditions. SBA-Pr-SO3H was proved to be an efficient heterogeneous nanoporous solid acid catalyst with a pore size of 6 nm, which could be easily handled and removed from the reaction mixture by simple filtration and can be recovered and reused several times without any loss of activity. The advantages of this methodology are high product yields, being environmentally benign, short reaction times, and easy handling. 相似文献