EDTA was used as an enhancer for Fe 2+ catalyzed light emission from luminol oxidation by dissolved oxygen. As a result, the limit of detection for ferrous ion with flow injection analysis was improved by a fact...EDTA was used as an enhancer for Fe 2+ catalyzed light emission from luminol oxidation by dissolved oxygen. As a result, the limit of detection for ferrous ion with flow injection analysis was improved by a factor of 160 by addition of EDTA to the luminol solution. Fe 2+ and Fe 3+ were determined simultaneously with a novel copper-coated zinc reductor minicolumn installed in one of the shunt after sample splitting in the manifold. The reductor minicolumn can be used for 3000 determinations at least. The dynamic range of determination was 1×10 -9 ～1×10 -5 mol·L -1 , with the limit of detection of 2.7×10 10 and 3.5×10 10 mol·L 1 ,for Fe 2+ and Fe 3+ , respectively. The preci sion for determination of 2×10 7 mol·L 1 of Fe 2+ and Fe 3+ was 2.3% and 4.0% (n=8), respectively, at a sampling rate of 60 h -1 . Cr 3+ and Co 2+ interfere. Fe 2+ and Fe 3+ in mixture were determined with satisfactory results. Samples of Fe 2+ and Fe 3+ were determined simultaneously and the results in good agreement with the standard spectrophotometric method. Indications were shown that EDTA functions as an enhancer, Fe 2+ as a catalyst, and oxygen is the oxidant of the chemiluminescent reaction, and the mechanism of the reaction was discussed.展开更多
A wet catalytic oxidation at room temperature was investigated with solution containing ferric, ferrous and cupric ions for H2S removal. The experiments were carried out in a two step process, and the results obtained...A wet catalytic oxidation at room temperature was investigated with solution containing ferric, ferrous and cupric ions for H2S removal. The experiments were carried out in a two step process, and the results obtained show that the removal efficiency of H2S can always reach 100% in a 300 mm scrubbing column with four sieve plates, and the regeneration of ferric ions in 200 mm bubble column can match the consumed ferric species in absorption. Removal of H2S, production of elemental sulfur and regeneration of ferric, cupric ions can all be accomplished at the same time. No raw material is consumed except O2 in flue gas or air, the process has no secondary pollution and no problem of catalyst degradation and congestion.展开更多
This paper is devoted to the study of the potentiality of the Fricke dosimeter for the characterization of the highly energetic (62.1 MeV) α particles beams generated by a new cyclotron facility, namely ARRONAX start...This paper is devoted to the study of the potentiality of the Fricke dosimeter for the characterization of the highly energetic (62.1 MeV) α particles beams generated by a new cyclotron facility, namely ARRONAX started in 2009. Such for this high energetic α beam, in situ dosimetry is performed in order to avoid radiation safety inconvenience and to earn run time of irradiation. Therefore, an in situ Fricke dosimetry protocol is developed and its reliability is checked by comparison with other experiments carried out by using the traditional method (ex situ Fricke dosimetry) within another cyclotron facility (CEMHTI) and by comparison with literature data. To author’s knowledge, it is the first time that Fricke dosimetry is performed during the α irradiation experiment. The results of these in situ dosimetry experiments show that the value of ferric ions radiolytic yield (G(Fe3+) = (11.7 ± 1.2) 10–7 mol?J–1) extrapolated from literature data can be used for this higher energy of α particles (Eα = 62.1 MeV).展开更多
A novel synthesis of LiFePO4/C from Fe2O3 with no extra carbon or carbon-containing reductant was introduced： Fe2O3 （＋NH4H2PO4）→Fe2P2O7（＋Li2CO3＋glucose）→LiFePO4/C. X-ray diffractometry （XRD）, Fourier trans...A novel synthesis of LiFePO4/C from Fe2O3 with no extra carbon or carbon-containing reductant was introduced： Fe2O3 （＋NH4H2PO4）→Fe2P2O7（＋Li2CO3＋glucose）→LiFePO4/C. X-ray diffractometry （XRD）, Fourier transform infrared spectroscopy （FTIR） and scanning electron microscopy （SEM） were utilized to characterize relevant products obtained in the synthetic procedure. The reaction of Fe2P2O7 and Li2CO3 was investigated by thermo-gravimetric and differential thermal analysis （TGA-DTA）. Fe2O3 is completely reduced to Fe2P2O7 by NH4H2PO4 at 700 ℃ and Fe2P2O7 fully reacts with Li2CO3 to form LiFePO4 in the temperature range of 663.4-890 ℃. The primary particles of LiFePO4/C samples prepared at 670, 700 and 750 ℃ respectively exhibit uniform morphology and narrow size distribution, 0.5-3 μm for those obtained at 670 and 700 ℃ and 0.5-5 μm for those obtained at 750 ℃. LiFePO4/C （carbon content of 5.49%, mass fraction） made at 670 ℃ shows an appreciable average capacity of 153.2 mA·h/g at 0.1C in the first 50 cycles.展开更多
Ferric and ferrous ion plays critical roles in bioprocesses,their influences in many fields have not been fully explored due to the lack of methods for quantification of ferric and ferrous ions in biological system or...Ferric and ferrous ion plays critical roles in bioprocesses,their influences in many fields have not been fully explored due to the lack of methods for quantification of ferric and ferrous ions in biological system or complex matrix.In this study,an M13 bacteriophage(phage) was engineered for use as a sensor for ferric and ferrous ions via the display of a tyrosine residue on the P8 coat protein.The interaction between the specific phenol group of tyrosine and Fe^(3+)./ Fe^(2+).was used as the sensor.Transmission electron microscopy showed aggregation of the tyrosine-displaying phages after incubation with Fe^(3+) and Fe^(2+).The aggregated phages infected the host bacterium inefficiently.This phenomenon could be utilized for detection of ferric and ferrous ions.For ferric ions,a calibration curve ranging from 200 nmol/L to 8 μmol/L with a detection limit of 58 nmol/L was acquired.For ferrous ions,a calibration curve ranging from 800 nmol/L to 8μmol/L with a detection limit of 641.7 nmol/L was acquired.The assay was specific for Fe^((3+)) and Fe^((2+)) when tested against Ni^(2+),Pb^(2+),Zn^(2+),Mn^(2+),Co^(2+),Ca^(2+),Cu^(2+),Cr^(3+),Ba^(2+),and K^+.The tyrosine displaying phage to Fe^(3+) and Fe^(2+) interaction would have plenty of room in application to biomatenals and bionanotechnology.展开更多
文摘EDTA was used as an enhancer for Fe 2+ catalyzed light emission from luminol oxidation by dissolved oxygen. As a result, the limit of detection for ferrous ion with flow injection analysis was improved by a factor of 160 by addition of EDTA to the luminol solution. Fe 2+ and Fe 3+ were determined simultaneously with a novel copper-coated zinc reductor minicolumn installed in one of the shunt after sample splitting in the manifold. The reductor minicolumn can be used for 3000 determinations at least. The dynamic range of determination was 1×10 -9 ～1×10 -5 mol·L -1 , with the limit of detection of 2.7×10 10 and 3.5×10 10 mol·L 1 ,for Fe 2+ and Fe 3+ , respectively. The preci sion for determination of 2×10 7 mol·L 1 of Fe 2+ and Fe 3+ was 2.3% and 4.0% (n=8), respectively, at a sampling rate of 60 h -1 . Cr 3+ and Co 2+ interfere. Fe 2+ and Fe 3+ in mixture were determined with satisfactory results. Samples of Fe 2+ and Fe 3+ were determined simultaneously and the results in good agreement with the standard spectrophotometric method. Indications were shown that EDTA functions as an enhancer, Fe 2+ as a catalyst, and oxygen is the oxidant of the chemiluminescent reaction, and the mechanism of the reaction was discussed.
文摘A wet catalytic oxidation at room temperature was investigated with solution containing ferric, ferrous and cupric ions for H2S removal. The experiments were carried out in a two step process, and the results obtained show that the removal efficiency of H2S can always reach 100% in a 300 mm scrubbing column with four sieve plates, and the regeneration of ferric ions in 200 mm bubble column can match the consumed ferric species in absorption. Removal of H2S, production of elemental sulfur and regeneration of ferric, cupric ions can all be accomplished at the same time. No raw material is consumed except O2 in flue gas or air, the process has no secondary pollution and no problem of catalyst degradation and congestion.
文摘This paper is devoted to the study of the potentiality of the Fricke dosimeter for the characterization of the highly energetic (62.1 MeV) α particles beams generated by a new cyclotron facility, namely ARRONAX started in 2009. Such for this high energetic α beam, in situ dosimetry is performed in order to avoid radiation safety inconvenience and to earn run time of irradiation. Therefore, an in situ Fricke dosimetry protocol is developed and its reliability is checked by comparison with other experiments carried out by using the traditional method (ex situ Fricke dosimetry) within another cyclotron facility (CEMHTI) and by comparison with literature data. To author’s knowledge, it is the first time that Fricke dosimetry is performed during the α irradiation experiment. The results of these in situ dosimetry experiments show that the value of ferric ions radiolytic yield (G(Fe3+) = (11.7 ± 1.2) 10–7 mol?J–1) extrapolated from literature data can be used for this higher energy of α particles (Eα = 62.1 MeV).
基金Project(2010ZC051)supported by the Natural Science Foundation of Yunnan Province,ChinaProject(2009-041)supported by Analysis and Testing Foundation from Kunming University of Science and Technology,ChinaProject(14118245)supported by the Starting Research Fund from Kunming University of Science and Technology,China
文摘A novel synthesis of LiFePO4/C from Fe2O3 with no extra carbon or carbon-containing reductant was introduced： Fe2O3 （＋NH4H2PO4）→Fe2P2O7（＋Li2CO3＋glucose）→LiFePO4/C. X-ray diffractometry （XRD）, Fourier transform infrared spectroscopy （FTIR） and scanning electron microscopy （SEM） were utilized to characterize relevant products obtained in the synthetic procedure. The reaction of Fe2P2O7 and Li2CO3 was investigated by thermo-gravimetric and differential thermal analysis （TGA-DTA）. Fe2O3 is completely reduced to Fe2P2O7 by NH4H2PO4 at 700 ℃ and Fe2P2O7 fully reacts with Li2CO3 to form LiFePO4 in the temperature range of 663.4-890 ℃. The primary particles of LiFePO4/C samples prepared at 670, 700 and 750 ℃ respectively exhibit uniform morphology and narrow size distribution, 0.5-3 μm for those obtained at 670 and 700 ℃ and 0.5-5 μm for those obtained at 750 ℃. LiFePO4/C （carbon content of 5.49%, mass fraction） made at 670 ℃ shows an appreciable average capacity of 153.2 mA·h/g at 0.1C in the first 50 cycles.
基金funded by the National Natural Science Foundation of China (No. 31300829)Natural Science Foundation of Hubei Province of China (No. 2014CFC1117)Open Research Fund Program of the State Key Laboratory of Virology of China (No. 2015IOV002)
文摘Ferric and ferrous ion plays critical roles in bioprocesses,their influences in many fields have not been fully explored due to the lack of methods for quantification of ferric and ferrous ions in biological system or complex matrix.In this study,an M13 bacteriophage(phage) was engineered for use as a sensor for ferric and ferrous ions via the display of a tyrosine residue on the P8 coat protein.The interaction between the specific phenol group of tyrosine and Fe^(3+)./ Fe^(2+).was used as the sensor.Transmission electron microscopy showed aggregation of the tyrosine-displaying phages after incubation with Fe^(3+) and Fe^(2+).The aggregated phages infected the host bacterium inefficiently.This phenomenon could be utilized for detection of ferric and ferrous ions.For ferric ions,a calibration curve ranging from 200 nmol/L to 8 μmol/L with a detection limit of 58 nmol/L was acquired.For ferrous ions,a calibration curve ranging from 800 nmol/L to 8μmol/L with a detection limit of 641.7 nmol/L was acquired.The assay was specific for Fe^((3+)) and Fe^((2+)) when tested against Ni^(2+),Pb^(2+),Zn^(2+),Mn^(2+),Co^(2+),Ca^(2+),Cu^(2+),Cr^(3+),Ba^(2+),and K^+.The tyrosine displaying phage to Fe^(3+) and Fe^(2+) interaction would have plenty of room in application to biomatenals and bionanotechnology.
