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L-Lysine was produced by a microbial process utilizing a Corynebacterium glutamicum (ATCC 21799) strain. L-Lysine was purified from the cultivated medium by fixed-bed and simulated moving bed (SMB) chromatography. The separation conditions including pH, eluent concentration and Lys+ and Lys2+ adsorption isotherms were studied in batch adsorption. The column capacity, eluent flow rate and eluent concentration have been studied in fixed-bed chromatography. Maximum purification rate of lysine was obtained as 0.066 g/(g·h) (per gram resin and per hour) at an eluent flow rate of 10 mL/min in fixed-bed chromatography. The results obtained from SMB were 0.11 g/(g·h) for L-lysine purification rate and 96% for L-lysine recovery. 相似文献
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Design and synthesis of a magnetic hierarchical porous organic polymer: A new platform in heterogeneous phase‐transfer catalysis
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Recyclable phase transfer catalysts containing magnetic nanoparticles (MNPs) have been known as a major trend towards sustainable catalysts. In this study, a novel class of magnetic porous polymer on the basis of calix[4]resorcinarene was synthesized starting from silica‐coated Fe3O4 core‐shell nanoparticles. This compound was found as an efficient phase transfer catalyst to the conversion of benzyl halides into benzyl azides and cyanides in good yields. The catalyst could be used at least for five consecutive cycles without appreciable loss in the catalytic activity. 相似文献
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Bahram Hasani Abbasali Zamani Mahdieh Koorepazan Moftakhar Maryam Mostafavi Mohammad Reza Yaftian Massomeh Ghorbanloo 《Journal of Analytical Chemistry》2018,73(1):82-90
Bis(2-hydroxybenzaldehyde)-1,2-diaminoethane (LI), bis(2-hydroxybenzaldehyde)-1,3-diaminopropane (LII) and bis(2-hydroxybenzaldehyde)-4,4'-methylendianiline (LIII) were examined as ionophores for fabrication of polyvinylchloride (PVC) membrane Cu(II) ion-selective potentiometric sensors. The optimum composition (%) for the sensors was: 5 LI, 30 PVC, 6 sodium tetraphenylborate (NaTPB), 59 ortho-nitrophenyloctyl ether (NPOE); 4 LII, 30 PVC, 5 NaTPB, 61 dibutyl phthalate; 6 LIII, 30 PVC, 5 NaTPB, 59 NPOE. The linear response range of the electrodes was 5 × 10–4–0.05 (LI), 5 × 10–4–0.1 (LII) and 1 × 10–6–0.01 M (LIII), and the corresponding detection limits were 4 × 10–4, 4 × 10–4 and 2 × 10–7 M, respectively. The sensors were showed rapid response time (≈10 s). Their responses were independent on pH in the range 2.5–5.0 (LI), 3.2–4.7 (LII) and 4.0–5.0 (LIII). The selectivity of the prepared electrodes towards copper ions over some mono-, di- and trivalent metal ions was evaluated. The sensors were used as indicator electrode in potentiometric titration of copper ions in aqueous solutions. 相似文献
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Mir Ali?FarajzadehEmail author Mortaza?Ebrahimi Ali?Ranji Elham?Feyz Vali?Bejani Ramin?Maleki 《Mikrochimica acta》2005,150(2):173-177
This study describes the sample preparation and two chromatographic techniques for determination of Tinuvin 622 in polyethylene. The first part of the two methods consisting of dissolving the polyethylene in boiling xylene is followed by addition of a methanolic solution of potassium hydroxide. The polymeric light stabilizer, Tinuvin 622, is thereby saponified to 4-hydroxy-2,2,6,6-tetramethyl-1-piperidineethanol (diol). Addition of the methanolic solution of the saponification reagent simultaneously precipitates the polyethylene matrix. Then the diol is quantified using either gas chromatography (GC) or high performance liquid chromatography (HPLC). For GC, a Macherey Nagel Optima-17 capillary column (30m×0.25mm ID, film thickness 0.25µm) is used. Nitrogen is used as carrier gas and make-up gas. The detection system is a flame ionization detector. For HPLC, an octadecyl silane (ODS) column (30cm×4mm, particle size 5µm) and a mobile phase methanol: water mixture (3:97, v/v) are used. Detection of analyte is carried out at 215nm. Both methods can be used to determine Tinuvin 622 in polyethylene in the concentration range of 0.02–1%, which represents the usual application concentration. 相似文献
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J. Khatouri M. Mostafavi J. Ridard J. Amblard J. Belloni 《Zeitschrift für Physik D Atoms, Molecules and Clusters》1995,34(1):47-56
The classical problem of the coalescence of isolated species to produce growing clusters/colloids/polymers by successive statistical encounters having the same rate constant, is revisited using numerical simulation for a maximum nuclearity value of a few 103 units. The evolution with time of the abundance of clusters of a given nuclearity and of the total population, and the distribution of sizes at a given time are obtained and compared with models from the literature. A remarkable feature of these curves is that they exhibit parity effects for the nuclearity, even clusters being systematically more abundant than odd ones. For easier comparison with experiments, some simulated curves are presented in the form of an approximated analytical expression: kinetics of the total population, and of the monomer, dimer and higher oligomers populations, amplitudes at the maximum and delay for the maximum as functions of the nuclearity, size distribution at a given time. The validity of the approximations is discussed. 相似文献
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In this work, the photocatalytic activity of the synthesized graphene oxide (GO)‐Fe3O4/TiO2 mesoporous photocatalysts was evaluated using chlorpyrifos (CP) as a contaminant. The nano‐photocatalyst was characterized by X‐ray diffraction, field emission scanning electron microscopy with energy‐dispersive X‐ray spectroscopy, transmission electron microscopy, and specific surface area by the Brunauer–Emmett–Teller method. Using visible light, the GO‐Fe3O4/TiO2 mesoporous photocatalyst was investigated on the degradation of CP pesticide. The GO‐Fe3O4/TiO2 photocatalyst displayed a good photocatalytic activity, which was achieving 97% of CP degradation after 60 min. Finally, experiments were performed to evaluate GO‐Fe3O4/TiO2 mesoporous nanocatalyst activity on repeated applications; after several uses, its photocatalytic activity was retained, which indicated stability. 相似文献
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Derakhshan M. Shamspur T. Molaakbari E. Mostafavi A. Saljooqi A. 《Russian Journal of Electrochemistry》2020,56(3):181-188
Russian Journal of Electrochemistry - In the present study an electrochemical sensor has been produced for measuring riboflavin with high sensitivity and selectivity. Deferential pulse technique... 相似文献
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This work assesses for the first time the potential of natural Kaolinite as adsorptive material for preconcentration of metal traces. Manganese is quantitatively retained by 2-(5-bromo-2-pyridylazo)-5-diethylaminophenol (5-Br-PADAP) on thermal modified Kaolinite by column method in pH range of 8.5-10.0 at flow rate of 2 ml min−1. Manganese was removed from column with 5.0 ml of H2SO4 4 mol l−1 and determined by flame atomic absorption spectrometric at 279.5 nm. In this case, 0.l μg of manganese can be concentrated from 800 ml of aqueous sample (where concentration is as low as 0.125 μg l−1). Detection limit is 4.3 μg l−1 (3 δbl m−1) and analytical curve is linear in the 0.02-10 mg l−1 in final solution with correlation coefficient 0.9997 and relative standard deviation for eight replicate determination of 5 μg of manganese in final solution is 0.71%. The interference of a large number of anions and cations has been studied in detail to optimize the conditions and method was successfully applied for determination of manganese in complex materials. 相似文献