On-line Cu （II） ion concentration detection in bioleaching system was achieved by anodic stripping differential pulse voltammetry （ASDPV）. Good linearity between Cu （II） concentration and oxidation peak current ...On-line Cu （II） ion concentration detection in bioleaching system was achieved by anodic stripping differential pulse voltammetry （ASDPV）. Good linearity between Cu （II） concentration and oxidation peak current was obtained when Cu （II） existed in 0K media in the concentration range of 1μmol/L （64μg/L） to 1 mmol/L （64 mg/L）. Moreover, when 0.2 mol/L KCl was added into this media, the linear detection range could be extended from 1 mmol/L to 100 mmol/L （6.4 g/L）. The reduction of Cu （II） to metallic copper was shown to proceed as two successive single-electron transfer reactions involving an intermediate chemical step where the cuprous ion （Cu＋） was complexed by chloride to form the dichlorocuprous anion （CuCl-）. In addition, interference effect was also investigated when Fe3＋existed in the media, which was the common situation in the copper bioleaching system. The results showed no interference effect once the concentration of Fe3＋was less than 100 mmol/L （5.6 g/L）.展开更多
The novel covalently modified glassy carbon electrode with poly(xylitol) was prepared using an electropolymerization technique for the simultaneous determination of uric acid(UA), xanthine(XA) and hypoxanthine(HX). Th...The novel covalently modified glassy carbon electrode with poly(xylitol) was prepared using an electropolymerization technique for the simultaneous determination of uric acid(UA), xanthine(XA) and hypoxanthine(HX). This new electrode presents an excellent electrocatalytic activity towards the oxidation of UA, XA and HX by cyclic voltammetry(CV) method. The oxidation peaks of the three compounds were well defined and had enhanced the peak currents. The separation potentials of the oxidation peak potentials for UA-XA and XA-HX were 380 and 370 mV in CV, respectively. Using differential pulse voltammetry(DPV) method, the calibration curves in the ranges of 5-55, 1.3-75.3 and 4-59 μmol/L were obtained for HX, XA and UA, respectively. The lowest detection limits(S/N=3) were 4.5, 0.75 and 3.75 μmol/L for HX, XA and UA, respectively. The practical application of the modified electrode was demonstrated by the determination of UA, XA, HX in human urine samples.展开更多
A new method was proposed for study of organic reducing substances in soils. According to the theoretical relationship between the voltammetric behaviors and reduction-oxidation reaction of reducing substances, the wo...A new method was proposed for study of organic reducing substances in soils. According to the theoretical relationship between the voltammetric behaviors and reduction-oxidation reaction of reducing substances, the working conditions of differential pulse voltammetry (d.p. v.) for determining the organic reducing substances produced during the processes of the anaerobic decomposition of plant materials were established with a glass carbon electrode as working electrode, 1 M Ag-AgCl electrode with large area as reference electrode, 0.2 M NH4AC as supporting electrolyte and pH buffer solution, pulse amplitude (AE) of 25 mV, scan rate at 2 mV·S-1and scan potential ranging from -0.5 to +1.2 voltage(vs. M Ag-AgCl). The peak current proportional to the concentration of reducing substances, and the characteristic peak potential of each organic reducing substance were regarded as the quantitative and qualitative base, respectively. These results obtained under the conditions mentioned above directly reflect both the reducing intensity and capacity of the organic reducing system in soils.展开更多
Based on theoretical calculation and Monte Carlo simulation,this paper proposes a new method for the diagnosing of 16.7 MeV high-energy pulse gamma,named "scattering absorption method". The ratio of the sens...Based on theoretical calculation and Monte Carlo simulation,this paper proposes a new method for the diagnosing of 16.7 MeV high-energy pulse gamma,named "scattering absorption method". The ratio of the sensitivity of high-energy gamma to that of the low-energy background gamma can reach 106 to 108 by this new method. The sensitivity of 16.7 MeV high-energy gamma ranges from 10-21 to 10-16 C·cm2. It's better than the traditional method which is based on the magnetic analyzer and Cherenkov detector on some aspects.展开更多
The graphene-gold nanoparticles composite film modified glassy carbon electrode （EG- AuNPs/GCE） was prepared by one-step coelectrodeposition and employed for determination of trace mercury in environmental water wit...The graphene-gold nanoparticles composite film modified glassy carbon electrode （EG- AuNPs/GCE） was prepared by one-step coelectrodeposition and employed for determination of trace mercury in environmental water with differential pulse stripping voltammetry. Such a nanostructured composite film combined with the advantages of gold nanoparticles and graphene, can greatly promote the electron-transfer process and increase accumulation abil-ity for Hg（Ⅱ）, leading to a remarkably improved sensitivity. The linear calibration curve ranged from 0.2 μg/L to 30 μg/L for Hg（Ⅱ） and the detection limit （S/N=3） was found to be 0.03 μg/L at a deposition time of 300 s. Moreover, the stablity of the as-prepared electrode and interferences from other substances were evaluated. The modified electrode was successfully applied to the direct detection of Hg（Ⅱ） in real water samples.展开更多
In this work,we reported a simultaneous determination approach for Pb(II),Cd(II)and Zn(II)atμg L 1concentration levels using differential pulse stripping voltammetry on a bismuth film electrode(BiFE).The BiFE could b...In this work,we reported a simultaneous determination approach for Pb(II),Cd(II)and Zn(II)atμg L 1concentration levels using differential pulse stripping voltammetry on a bismuth film electrode(BiFE).The BiFE could be prepared in situ when the sample solution contained a suitable amount of Bi(NO)3,and its analytical performance was evaluated for the simultaneous determination of Pb(II),Cd(II)and Zn(II)in solutions.The determination limits were found to be 0.19μg L 1for Zn(II),and0.28μg L 1for Pb(II)and Cd(II),with a preconcentration time of 300 s.The BiFE approach was successfully applied to determine Pb(II),Cd(II)and Zn(II)in tea leaf and infusion samples,and the results were in agreement with those obtained using an atomic absorption spectrometry approach.Without Hg usage,the in situ preparation for BiFE supplied a green and acceptability sensitive method for the determination of the heavy metal ions.展开更多
基金Projects(2012CB933303,2011CB707505)supported by the National Basic Research Program of ChinaProject(2012BAK08B05)supported by the National Key Technology R&D Program of China+1 种基金Projects(11391901900,11530700800,10391901600,201101042,11CH-15)supported by Science and Technology Commission of Shanghai Municipality,ChinaProject supported by Funding from CSIRO CEO Science Leader Program
文摘On-line Cu （II） ion concentration detection in bioleaching system was achieved by anodic stripping differential pulse voltammetry （ASDPV）. Good linearity between Cu （II） concentration and oxidation peak current was obtained when Cu （II） existed in 0K media in the concentration range of 1μmol/L （64μg/L） to 1 mmol/L （64 mg/L）. Moreover, when 0.2 mol/L KCl was added into this media, the linear detection range could be extended from 1 mmol/L to 100 mmol/L （6.4 g/L）. The reduction of Cu （II） to metallic copper was shown to proceed as two successive single-electron transfer reactions involving an intermediate chemical step where the cuprous ion （Cu＋） was complexed by chloride to form the dichlorocuprous anion （CuCl-）. In addition, interference effect was also investigated when Fe3＋existed in the media, which was the common situation in the copper bioleaching system. The results showed no interference effect once the concentration of Fe3＋was less than 100 mmol/L （5.6 g/L）.
基金Project(201215135) supported by the Natural Science Foundation of Jilin Province,China
文摘The novel covalently modified glassy carbon electrode with poly(xylitol) was prepared using an electropolymerization technique for the simultaneous determination of uric acid(UA), xanthine(XA) and hypoxanthine(HX). This new electrode presents an excellent electrocatalytic activity towards the oxidation of UA, XA and HX by cyclic voltammetry(CV) method. The oxidation peaks of the three compounds were well defined and had enhanced the peak currents. The separation potentials of the oxidation peak potentials for UA-XA and XA-HX were 380 and 370 mV in CV, respectively. Using differential pulse voltammetry(DPV) method, the calibration curves in the ranges of 5-55, 1.3-75.3 and 4-59 μmol/L were obtained for HX, XA and UA, respectively. The lowest detection limits(S/N=3) were 4.5, 0.75 and 3.75 μmol/L for HX, XA and UA, respectively. The practical application of the modified electrode was demonstrated by the determination of UA, XA, HX in human urine samples.
文摘A new method was proposed for study of organic reducing substances in soils. According to the theoretical relationship between the voltammetric behaviors and reduction-oxidation reaction of reducing substances, the working conditions of differential pulse voltammetry (d.p. v.) for determining the organic reducing substances produced during the processes of the anaerobic decomposition of plant materials were established with a glass carbon electrode as working electrode, 1 M Ag-AgCl electrode with large area as reference electrode, 0.2 M NH4AC as supporting electrolyte and pH buffer solution, pulse amplitude (AE) of 25 mV, scan rate at 2 mV·S-1and scan potential ranging from -0.5 to +1.2 voltage(vs. M Ag-AgCl). The peak current proportional to the concentration of reducing substances, and the characteristic peak potential of each organic reducing substance were regarded as the quantitative and qualitative base, respectively. These results obtained under the conditions mentioned above directly reflect both the reducing intensity and capacity of the organic reducing system in soils.
文摘Based on theoretical calculation and Monte Carlo simulation,this paper proposes a new method for the diagnosing of 16.7 MeV high-energy pulse gamma,named "scattering absorption method". The ratio of the sensitivity of high-energy gamma to that of the low-energy background gamma can reach 106 to 108 by this new method. The sensitivity of 16.7 MeV high-energy gamma ranges from 10-21 to 10-16 C·cm2. It's better than the traditional method which is based on the magnetic analyzer and Cherenkov detector on some aspects.
文摘The graphene-gold nanoparticles composite film modified glassy carbon electrode （EG- AuNPs/GCE） was prepared by one-step coelectrodeposition and employed for determination of trace mercury in environmental water with differential pulse stripping voltammetry. Such a nanostructured composite film combined with the advantages of gold nanoparticles and graphene, can greatly promote the electron-transfer process and increase accumulation abil-ity for Hg（Ⅱ）, leading to a remarkably improved sensitivity. The linear calibration curve ranged from 0.2 μg/L to 30 μg/L for Hg（Ⅱ） and the detection limit （S/N=3） was found to be 0.03 μg/L at a deposition time of 300 s. Moreover, the stablity of the as-prepared electrode and interferences from other substances were evaluated. The modified electrode was successfully applied to the direct detection of Hg（Ⅱ） in real water samples.
基金supported by the National Natural Scientific Foundation of China(21175112)the Fund of Key Laboratory of Global Change and Marine-Atmospheric Chemistry,SOA,(GCMAC 1204)the Fujian Key Projects of Science and Technology(2011YZ0001-1)
文摘In this work,we reported a simultaneous determination approach for Pb(II),Cd(II)and Zn(II)atμg L 1concentration levels using differential pulse stripping voltammetry on a bismuth film electrode(BiFE).The BiFE could be prepared in situ when the sample solution contained a suitable amount of Bi(NO)3,and its analytical performance was evaluated for the simultaneous determination of Pb(II),Cd(II)and Zn(II)in solutions.The determination limits were found to be 0.19μg L 1for Zn(II),and0.28μg L 1for Pb(II)and Cd(II),with a preconcentration time of 300 s.The BiFE approach was successfully applied to determine Pb(II),Cd(II)and Zn(II)in tea leaf and infusion samples,and the results were in agreement with those obtained using an atomic absorption spectrometry approach.Without Hg usage,the in situ preparation for BiFE supplied a green and acceptability sensitive method for the determination of the heavy metal ions.
