SrMoO4 nanoplates were synthesized by a facile reverse microemulsion method at room temperature.Energy evolution of this in situ growth process was monitored by means of a microcalorimeter.A sharp exothermic peak for ...SrMoO4 nanoplates were synthesized by a facile reverse microemulsion method at room temperature.Energy evolution of this in situ growth process was monitored by means of a microcalorimeter.A sharp exothermic peak for the initial reaction and two discontinuous relatively weak exothermic peaks for the subsequent crystal growth emerged on the microcalorimetric heat flow curve.Based on the in situ thermokinetic data,the rate constants of the nucleation process and crystallization process at 298.15 K were calculated to be 4.078×10-3 and 5.033×10-4 s-1,respectively.The growth mechanism and energy evolution were investigated.展开更多
A novel third-generation hydrogen peroxide（H2O2） biosensor（Hb/CdS/MWNTs/GCE） was fabricated through hemoglobin（Hb） adsorbed onto the mercaptoacetic acid modified CdS QDs/carboxyl multiwall carbon nanotubes＇（MW...A novel third-generation hydrogen peroxide（H2O2） biosensor（Hb/CdS/MWNTs/GCE） was fabricated through hemoglobin（Hb） adsorbed onto the mercaptoacetic acid modified CdS QDs/carboxyl multiwall carbon nanotubes＇（MWNTs） films. Cyclic voltammogram of Hb/CdS/MWNTs/GCE showed a pair of well-defined and quasi-reversible redox peaks with a formal potential（E^0） of-0.230 V（vs. Ag/AgCl） in 0.1 mol/L pH=8.0 phosphate buffer solution（PBS）, which was the characteristic of the Hb heme Fe（Ⅲ）/Fe（Ⅱ） redox couple. The biosensor shows an excellent electrocatalytic activity to the reduction of H2O2. The response time of the designed biosensor to H202 at a potential of-0.30 V was less than 2 s and linear relationships were obtained in the concentration ranges of 2.0×10^-6-2.7×10^-3 mol/L and 2.7×10^-3-7.7×10^-3 mol/L with a detection limit of 3.0×10^-7 mol/L（S/N=3）. The apparent Michaelis-Menten constant Km was estimated to be 1.324 mmol/L that illustrated the excellent biological activity of the fixed Hb.展开更多
Molecularly imprinted polymers（MIPs） were applied as molecular recognition elements to an electro- chemical sensor for cinchonidine（CD）. A kind of MIP was synthesized with cinchonidine as template, modified ro- si...Molecularly imprinted polymers（MIPs） were applied as molecular recognition elements to an electro- chemical sensor for cinchonidine（CD）. A kind of MIP was synthesized with cinchonidine as template, modified ro- sin（ethylene glycol maleic rosinate acrylate） containing the skeleton of phenanthrene rings as cross-linker and me- thylacrylic acid as functional monomer. MIP membrane was prepared on a glassy carbon electrode for the determina- tion of CD via free radical polymerization method. Electrochemical impedance spectroscopy（EIS） and cyclic vol- tammetry（CV） were used to characterize the membrane electrochemical behavior in electrode fabrication process. The experimental conditions were discussed. Under optimum conditions, it was found that the response of peak cur- rents was linear to the concentration of CD in a range of 0.013-2.26 mmol/L. The detection limit for CD is 1 μmol/L the relative standard deviation for 100 μmol/L CD is 1.34% and the incubation time is 2 min. The sensor was applied to the determination of CD in urine samples with satisfactory results.展开更多
基金Supported by the National Natural Science Foundation of China(No.20963001)the Major Project of Natural Science Foundation of Guangxi Province,China(No.0991001Z)
文摘SrMoO4 nanoplates were synthesized by a facile reverse microemulsion method at room temperature.Energy evolution of this in situ growth process was monitored by means of a microcalorimeter.A sharp exothermic peak for the initial reaction and two discontinuous relatively weak exothermic peaks for the subsequent crystal growth emerged on the microcalorimetric heat flow curve.Based on the in situ thermokinetic data,the rate constants of the nucleation process and crystallization process at 298.15 K were calculated to be 4.078×10-3 and 5.033×10-4 s-1,respectively.The growth mechanism and energy evolution were investigated.
基金Supported by the Natural Science Foundation of Guangxi Province,China(Nos.0639025 and 0991084)the Support Program for 100 Young and Middle-aged Disciplinary Leaders in Higher Education Institutions of Guangxi Province,China(No. RC20060703005)+2 种基金the Key Laboratory of Development and Application of Forest Chemicals of Guangxi Province,China (No.GXFC08-06)the Education Department of Guangxi Province,China(No.200807MS074)the Innovation Project of Guangxi University fot Nationalities,China(No.gxun-chx2009081)
文摘A novel third-generation hydrogen peroxide（H2O2） biosensor（Hb/CdS/MWNTs/GCE） was fabricated through hemoglobin（Hb） adsorbed onto the mercaptoacetic acid modified CdS QDs/carboxyl multiwall carbon nanotubes＇（MWNTs） films. Cyclic voltammogram of Hb/CdS/MWNTs/GCE showed a pair of well-defined and quasi-reversible redox peaks with a formal potential（E^0） of-0.230 V（vs. Ag/AgCl） in 0.1 mol/L pH=8.0 phosphate buffer solution（PBS）, which was the characteristic of the Hb heme Fe（Ⅲ）/Fe（Ⅱ） redox couple. The biosensor shows an excellent electrocatalytic activity to the reduction of H2O2. The response time of the designed biosensor to H202 at a potential of-0.30 V was less than 2 s and linear relationships were obtained in the concentration ranges of 2.0×10^-6-2.7×10^-3 mol/L and 2.7×10^-3-7.7×10^-3 mol/L with a detection limit of 3.0×10^-7 mol/L（S/N=3）. The apparent Michaelis-Menten constant Km was estimated to be 1.324 mmol/L that illustrated the excellent biological activity of the fixed Hb.
基金Supported by the National Nature Science Foundation of China(Nos.21065001 and 30960306)the Natural Science Foundation of Guangxi Province,China(Nos.0639025,0991084 and 0991001z)+2 种基金the Fund of Guangxi Key Laboratory of Chemistry and Engineering of Forest Products,China(No.GXFC08-06)the Project of Education Department of Guangxi Province,China(No.200812MS074)the Innovation Project of Guangxi University for Nationalities,China(No.gxun-chx2011086)
文摘Molecularly imprinted polymers（MIPs） were applied as molecular recognition elements to an electro- chemical sensor for cinchonidine（CD）. A kind of MIP was synthesized with cinchonidine as template, modified ro- sin（ethylene glycol maleic rosinate acrylate） containing the skeleton of phenanthrene rings as cross-linker and me- thylacrylic acid as functional monomer. MIP membrane was prepared on a glassy carbon electrode for the determina- tion of CD via free radical polymerization method. Electrochemical impedance spectroscopy（EIS） and cyclic vol- tammetry（CV） were used to characterize the membrane electrochemical behavior in electrode fabrication process. The experimental conditions were discussed. Under optimum conditions, it was found that the response of peak cur- rents was linear to the concentration of CD in a range of 0.013-2.26 mmol/L. The detection limit for CD is 1 μmol/L the relative standard deviation for 100 μmol/L CD is 1.34% and the incubation time is 2 min. The sensor was applied to the determination of CD in urine samples with satisfactory results.
