The micro-amount of nickel in MnO2, electrolytical and natural both, was determined by differential pulse polarography. NH4OH-NH4Cl was used as supporting electrolyte. It was found that the peak potential of Ni(II) re...The micro-amount of nickel in MnO2, electrolytical and natural both, was determined by differential pulse polarography. NH4OH-NH4Cl was used as supporting electrolyte. It was found that the peak potential of Ni(II) reduction wave is -1.0V (vs. Ag-AgCl electrode). The presence of great amount of Mn(II) does not interfere in the trace nickel determination. the peak current relationship with the Ni2+ concentration presents a quite fine straight line. The differential pulse polarography is proved that it is a simple, reliable and acceptable method for determination of trace Ni in various species of MnO2.展开更多
The polarographic adsorptive complex wave of rare earths (RE) with 1-phenyl-3-methyl-4-benzoylpyrazoione-5 (PMBP) was studied in HAc-NaAc medium at pH=3.80. In the singlesweep polarography, the reduction potential of ...The polarographic adsorptive complex wave of rare earths (RE) with 1-phenyl-3-methyl-4-benzoylpyrazoione-5 (PMBP) was studied in HAc-NaAc medium at pH=3.80. In the singlesweep polarography, the reduction potential of complex wave (-1.16V) is more negative than that of the free ligand. (-1.12V), and the wave was proven to be an adsorptive complex wave by cyclic voltammetry method. This experiment proved that only the complexes of heavy RE ions can be adsorbed on the electrode under the same conditions. So it is a good method to determine heavy rare earths in the presence of light rare earths.展开更多
The cathodic wave of vitamin C has not been reported in the literature so far.Its E_(1/2)was found at-1.85 volt vs.Ag/AgCl(25℃)in the base solution of 0.1mol/L Bu_4NI.Various electrochemical and spectral techniques w...The cathodic wave of vitamin C has not been reported in the literature so far.Its E_(1/2)was found at-1.85 volt vs.Ag/AgCl(25℃)in the base solution of 0.1mol/L Bu_4NI.Various electrochemical and spectral techniques were used for studying the electrode reaction. They all showed that the electrode reaction was quasi-reversible while C was more than 1.0×10^(-6)mol/L and mainly adsorptive while C was less than 1.0×10^(-6)mol/L at a mercury electrode.The electron transfer number was 2 and the electron transfer coefficient 0.57. Using DPP techniques,the linear response range was 5.0×10^(-7)-2.0×10^(-3)mol/L and the detection limit 1×10^(-7)mol/L.展开更多
Polarographic characteristics of Te(Ⅳ)-alkaline dye were investiga- ted at mercury electrode in acidic solution.It was found that the mechanism of the electrode process depended on the concentration of Te(Ⅳ).
It is reported in this paper a polarographic catalytic double wave of oxygen reduction caused by diphenylamine compounds(diphs).The electrochemical process of the wave includes the polarographic generation of the supe...It is reported in this paper a polarographic catalytic double wave of oxygen reduction caused by diphenylamine compounds(diphs).The electrochemical process of the wave includes the polarographic generation of the superoxide anion O_2^- and the dismutation of O_2^- catalyzed by diphs with redox pseudoreversibility.展开更多
This paper reports a polarographic catalytic wave of lysozyme (LE) in the presence of KIO3. The mechanism of the catalytic wave was discussed. It is illustrated by the catalytic wave of LE that, besides the Brdicka cu...This paper reports a polarographic catalytic wave of lysozyme (LE) in the presence of KIO3. The mechanism of the catalytic wave was discussed. It is illustrated by the catalytic wave of LE that, besides the Brdicka current, there exists a new kind of catalytic wave of protein.展开更多
The sensitive second derivative waves of Cu(Ⅱ),Pb(Ⅱ),Cd(Ⅱ),Ni(Ⅱ),Zn(Ⅱ),Fe(Ⅱ)and Mn(Ⅱ),forming in the substrate solution(pH=9.26)consisting of ammonia,ammonium chlorid,gelatin and ascorbic acid were researched.T...The sensitive second derivative waves of Cu(Ⅱ),Pb(Ⅱ),Cd(Ⅱ),Ni(Ⅱ),Zn(Ⅱ),Fe(Ⅱ)and Mn(Ⅱ),forming in the substrate solution(pH=9.26)consisting of ammonia,ammonium chlorid,gelatin and ascorbic acid were researched.The peak potentials of the polarographic waves of the seven ions are at about 0.48,0.63,0.79,1.04,1.28,1.44 and 1.60 V respectively.Combining with microwave technique,a new method for the simultaneous determination of the seven trace elements in Chinese traditional medicine was developed.The method is easy to operate,rapid,simple and convenient.When the signal-to-noise rate equals 3,the detection limits of Cu,Pb,Cd,Ni,Zn,Fe and Mn are 4.2×10 3,5.3×10 3,2.1×10 3,5.8×10 4,3.0×10 3,7.7×10 4 and 1.1×10 3 μg/mL respectively.Well linear relationships exist between the concentrations and the peak currents when Cu,Pb,Cd,Ni,Zn,Fe and Mn concentrations are within 8.5×10 3 10,9.7×10 3 10,4.5×10 3 10,1.2×10 3 10,6.4×10 3 10,1.5×10 3 10 and 2.8×10 3 10 μg/mL,respectively.The method has been used to the simultaneous determination of the seven trace elements in Salvia Miltiorrhiza Root and compound Salvia Miltiorrhiza Root injection,the relative standard deviations(RSDs)of the Cu,Pb,Cd,Ni,Zn,Fe and Mn in the two medicines are 3.9% and 5.8%,4.0% and 4.1%,4.3% and 5.7%,4.9% and 5.3%,4.4% and 4.7%,3.5% and 4.0%,0.51% and 2.8%,respectively;the comparisons of the determination results with the values obtained by the standard method indicate that the presented method has very well veracity.展开更多
A new method has been developed to assay poly(ADP-ribose) polymerase (PARP) activity in plant tissues through determining the content of nicotinamide (NIC) produced by enzymatic reaction by linear sweeping polarograph...A new method has been developed to assay poly(ADP-ribose) polymerase (PARP) activity in plant tissues through determining the content of nicotinamide (NIC) produced by enzymatic reaction by linear sweeping polarographic method. The detection limit of NIC was 0.03μmol/L, the calibration graph was linear up to 5μmol/L ( r = 0.999). The recoveries were approximately in the range of 92% to 98% and the relative standard deviations were less展开更多
Polarographic catalytic wave of chlordiazepoxide in the presence of K 2S 2O 8 was studied in aqueous and DMF/H 2O mixed solutions. The results showed that a single reduction wave in alkaline medium was the reducti...Polarographic catalytic wave of chlordiazepoxide in the presence of K 2S 2O 8 was studied in aqueous and DMF/H 2O mixed solutions. The results showed that a single reduction wave in alkaline medium was the reduction of the N=C bond in 1,2 position of chlordiazepoxide via an intermediate free radical in two one electron successive additions. When K 2S 2O 8 was present, the free radical of the N=C bond was oxidized to regenerate the original, producing a parallel catalytic wave of chlordiazepoxide. It was determined that the apparent rate constant k f of the oxidation reaction was 3.2×10 3 mol -1 ·L·s -1 . Using the catalytic wave the trace of chlordiazepoxide can be determined by linear potential scan polarography. In NH 3/NH 4Cl (pH 10.2±0.1, 0.12 mol/L)/K 2S 2O 8 (0.016 mol/L) supporting electrolyte, the second order derivative peak current of the catalytic wave was rectilinear to chlordiazepoxide concentration in the range of 3.20×10 -8 -1.60×10 -7 , 1.60×10 -7 -1.44×10 -6 and 1.44 ×10 -6 -1.44×10 -5 mol/L, respectively. The limit of detection was 9.0×10 -9 mol/L.展开更多
The polarographic behavior and catalytic wave mechanism of medroprogesterone acetate （MPA） were studied in both aqueous and DMF media. In 0.2 mol/L acetic acid-sodium acetate （pH 5.0） buffer solution, the C=C bond...The polarographic behavior and catalytic wave mechanism of medroprogesterone acetate （MPA） were studied in both aqueous and DMF media. In 0.2 mol/L acetic acid-sodium acetate （pH 5.0） buffer solution, the C=C bond of MPA first undergoes le, lH<sup>+</sup> reduction to form protonated free radical HMPA（?）, the further reduction of HMPA（?） in le, 1H<sup>+</sup> process is simultaneous with the dimerization reaction between HMPA（?） and neutral molecular MPA. In DMF media containing 0.1 mol/L tetrabutylammonium tetrafluoborate （TBA·BF<sub>4</sub>）, the C=C bond of MPA shows two le, 1H<sup>+</sup> reduction waves, which are ascribed to the reduction of MPA and free radical MPA, respectively. Here, no dimerization reaction occurs. These processes produce the reduction wave of MPA. In the presence of oxidant KIO<sub>3</sub>, a polarographic catalytic wave of MPA is observable due to a chemical reaction between HMPA（?） or MPA（?） and KIO<sub>3</sub> as well as its intermediate species to regenerate MPA. The catalytic wave, which is caused by the reduction of organic展开更多
The polarographic catalytic wave of oxygen reduction caused by mefenamic acid （MA） with redox properties was reported in this paper. The electrochemical process of the catalytic wave was proposed that the superoxide...The polarographic catalytic wave of oxygen reduction caused by mefenamic acid （MA） with redox properties was reported in this paper. The electrochemical process of the catalytic wave was proposed that the superoxide anion O（?） was generated polarographically and the dismutation of the O（?） was catalyzed by MA to reproduce O<sub>2</sub> and H<sub>2</sub>O<sub>2</sub>. This explained chemically the scavenging of the O<sub>2</sub><sup>-</sup> by MA im biomedical area. Based on the catalytic wave, a new method for the determination of MA by single-sweep polarography was developed.展开更多
In our previous papers, the isonuclear complexes of RE (Ⅲ)-Ni (Ⅱ) (or Co(Ⅱ))-ALC had been studied by single-sweep polarograph. In the present note, the polarographic adsorptive complex wave of RE (Ⅲ)-Cu (Ⅱ)-ALC i...In our previous papers, the isonuclear complexes of RE (Ⅲ)-Ni (Ⅱ) (or Co(Ⅱ))-ALC had been studied by single-sweep polarograph. In the present note, the polarographic adsorptive complex wave of RE (Ⅲ)-Cu (Ⅱ)-ALC is reported. The mechanisms of the two are different, the former being the reduced wave of ligand (ALC),展开更多
The rare earth ions form complexes with ECAB in 0.1 mol/L NaAc-HAc supporting electrolyte at pH 6. The composition of the complex was determined by spectrophotometric method to be 1: 2. The decrease of SAC peak height...The rare earth ions form complexes with ECAB in 0.1 mol/L NaAc-HAc supporting electrolyte at pH 6. The composition of the complex was determined by spectrophotometric method to be 1: 2. The decrease of SAC peak height of ECAB is proportional to the concentration of rare earth ions in the range of 1×10<sup>-6</sup>-2×10<sup>-5</sup> mol/L. The reduction mechanism of ECAB and RE-ECAB is proposed based on the experimental evidence. The complexing group of ECAB with RE ions iust is the redox group, so when RE ions are added, there is no new peak appearing in the polarograms:, the only phenomenon observed is that the peak current of ECAB decreases. The fast protonation of EGAB carbanion formed after the second electron transfer results in the formation of colourless tetrahedral molecules.展开更多
文摘The micro-amount of nickel in MnO2, electrolytical and natural both, was determined by differential pulse polarography. NH4OH-NH4Cl was used as supporting electrolyte. It was found that the peak potential of Ni(II) reduction wave is -1.0V (vs. Ag-AgCl electrode). The presence of great amount of Mn(II) does not interfere in the trace nickel determination. the peak current relationship with the Ni2+ concentration presents a quite fine straight line. The differential pulse polarography is proved that it is a simple, reliable and acceptable method for determination of trace Ni in various species of MnO2.
文摘The polarographic adsorptive complex wave of rare earths (RE) with 1-phenyl-3-methyl-4-benzoylpyrazoione-5 (PMBP) was studied in HAc-NaAc medium at pH=3.80. In the singlesweep polarography, the reduction potential of complex wave (-1.16V) is more negative than that of the free ligand. (-1.12V), and the wave was proven to be an adsorptive complex wave by cyclic voltammetry method. This experiment proved that only the complexes of heavy RE ions can be adsorbed on the electrode under the same conditions. So it is a good method to determine heavy rare earths in the presence of light rare earths.
基金Project supported by National Natural Science Foundation of P.R.China and by Foundation of Lab of Electroanalytical Chemistry,Changchun Institute of Applied Chemistry,Academia Sinica
文摘The cathodic wave of vitamin C has not been reported in the literature so far.Its E_(1/2)was found at-1.85 volt vs.Ag/AgCl(25℃)in the base solution of 0.1mol/L Bu_4NI.Various electrochemical and spectral techniques were used for studying the electrode reaction. They all showed that the electrode reaction was quasi-reversible while C was more than 1.0×10^(-6)mol/L and mainly adsorptive while C was less than 1.0×10^(-6)mol/L at a mercury electrode.The electron transfer number was 2 and the electron transfer coefficient 0.57. Using DPP techniques,the linear response range was 5.0×10^(-7)-2.0×10^(-3)mol/L and the detection limit 1×10^(-7)mol/L.
基金Project Supported by National Natural Scientific Foundation of China
文摘Polarographic characteristics of Te(Ⅳ)-alkaline dye were investiga- ted at mercury electrode in acidic solution.It was found that the mechanism of the electrode process depended on the concentration of Te(Ⅳ).
文摘It is reported in this paper a polarographic catalytic double wave of oxygen reduction caused by diphenylamine compounds(diphs).The electrochemical process of the wave includes the polarographic generation of the superoxide anion O_2^- and the dismutation of O_2^- catalyzed by diphs with redox pseudoreversibility.
文摘This paper reports a polarographic catalytic wave of lysozyme (LE) in the presence of KIO3. The mechanism of the catalytic wave was discussed. It is illustrated by the catalytic wave of LE that, besides the Brdicka current, there exists a new kind of catalytic wave of protein.
基金Proejcr(20235020) supported by the National Natural Science Foundation of China
文摘The sensitive second derivative waves of Cu(Ⅱ),Pb(Ⅱ),Cd(Ⅱ),Ni(Ⅱ),Zn(Ⅱ),Fe(Ⅱ)and Mn(Ⅱ),forming in the substrate solution(pH=9.26)consisting of ammonia,ammonium chlorid,gelatin and ascorbic acid were researched.The peak potentials of the polarographic waves of the seven ions are at about 0.48,0.63,0.79,1.04,1.28,1.44 and 1.60 V respectively.Combining with microwave technique,a new method for the simultaneous determination of the seven trace elements in Chinese traditional medicine was developed.The method is easy to operate,rapid,simple and convenient.When the signal-to-noise rate equals 3,the detection limits of Cu,Pb,Cd,Ni,Zn,Fe and Mn are 4.2×10 3,5.3×10 3,2.1×10 3,5.8×10 4,3.0×10 3,7.7×10 4 and 1.1×10 3 μg/mL respectively.Well linear relationships exist between the concentrations and the peak currents when Cu,Pb,Cd,Ni,Zn,Fe and Mn concentrations are within 8.5×10 3 10,9.7×10 3 10,4.5×10 3 10,1.2×10 3 10,6.4×10 3 10,1.5×10 3 10 and 2.8×10 3 10 μg/mL,respectively.The method has been used to the simultaneous determination of the seven trace elements in Salvia Miltiorrhiza Root and compound Salvia Miltiorrhiza Root injection,the relative standard deviations(RSDs)of the Cu,Pb,Cd,Ni,Zn,Fe and Mn in the two medicines are 3.9% and 5.8%,4.0% and 4.1%,4.3% and 5.7%,4.9% and 5.3%,4.4% and 4.7%,3.5% and 4.0%,0.51% and 2.8%,respectively;the comparisons of the determination results with the values obtained by the standard method indicate that the presented method has very well veracity.
文摘A new method has been developed to assay poly(ADP-ribose) polymerase (PARP) activity in plant tissues through determining the content of nicotinamide (NIC) produced by enzymatic reaction by linear sweeping polarographic method. The detection limit of NIC was 0.03μmol/L, the calibration graph was linear up to 5μmol/L ( r = 0.999). The recoveries were approximately in the range of 92% to 98% and the relative standard deviations were less
文摘Polarographic catalytic wave of chlordiazepoxide in the presence of K 2S 2O 8 was studied in aqueous and DMF/H 2O mixed solutions. The results showed that a single reduction wave in alkaline medium was the reduction of the N=C bond in 1,2 position of chlordiazepoxide via an intermediate free radical in two one electron successive additions. When K 2S 2O 8 was present, the free radical of the N=C bond was oxidized to regenerate the original, producing a parallel catalytic wave of chlordiazepoxide. It was determined that the apparent rate constant k f of the oxidation reaction was 3.2×10 3 mol -1 ·L·s -1 . Using the catalytic wave the trace of chlordiazepoxide can be determined by linear potential scan polarography. In NH 3/NH 4Cl (pH 10.2±0.1, 0.12 mol/L)/K 2S 2O 8 (0.016 mol/L) supporting electrolyte, the second order derivative peak current of the catalytic wave was rectilinear to chlordiazepoxide concentration in the range of 3.20×10 -8 -1.60×10 -7 , 1.60×10 -7 -1.44×10 -6 and 1.44 ×10 -6 -1.44×10 -5 mol/L, respectively. The limit of detection was 9.0×10 -9 mol/L.
基金Project supported by the National Natural Science Foundation of China (Grant No. 29875017).
文摘The polarographic behavior and catalytic wave mechanism of medroprogesterone acetate （MPA） were studied in both aqueous and DMF media. In 0.2 mol/L acetic acid-sodium acetate （pH 5.0） buffer solution, the C=C bond of MPA first undergoes le, lH<sup>+</sup> reduction to form protonated free radical HMPA（?）, the further reduction of HMPA（?） in le, 1H<sup>+</sup> process is simultaneous with the dimerization reaction between HMPA（?） and neutral molecular MPA. In DMF media containing 0.1 mol/L tetrabutylammonium tetrafluoborate （TBA·BF<sub>4</sub>）, the C=C bond of MPA shows two le, 1H<sup>+</sup> reduction waves, which are ascribed to the reduction of MPA and free radical MPA, respectively. Here, no dimerization reaction occurs. These processes produce the reduction wave of MPA. In the presence of oxidant KIO<sub>3</sub>, a polarographic catalytic wave of MPA is observable due to a chemical reaction between HMPA（?） or MPA（?） and KIO<sub>3</sub> as well as its intermediate species to regenerate MPA. The catalytic wave, which is caused by the reduction of organic
文摘The polarographic catalytic wave of oxygen reduction caused by mefenamic acid （MA） with redox properties was reported in this paper. The electrochemical process of the catalytic wave was proposed that the superoxide anion O（?） was generated polarographically and the dismutation of the O（?） was catalyzed by MA to reproduce O<sub>2</sub> and H<sub>2</sub>O<sub>2</sub>. This explained chemically the scavenging of the O<sub>2</sub><sup>-</sup> by MA im biomedical area. Based on the catalytic wave, a new method for the determination of MA by single-sweep polarography was developed.
基金Project supported by the National Natural Science Foundation of China
文摘In our previous papers, the isonuclear complexes of RE (Ⅲ)-Ni (Ⅱ) (or Co(Ⅱ))-ALC had been studied by single-sweep polarograph. In the present note, the polarographic adsorptive complex wave of RE (Ⅲ)-Cu (Ⅱ)-ALC is reported. The mechanisms of the two are different, the former being the reduced wave of ligand (ALC),
基金Project supported by the National Natural Science Foundation of China
文摘The rare earth ions form complexes with ECAB in 0.1 mol/L NaAc-HAc supporting electrolyte at pH 6. The composition of the complex was determined by spectrophotometric method to be 1: 2. The decrease of SAC peak height of ECAB is proportional to the concentration of rare earth ions in the range of 1×10<sup>-6</sup>-2×10<sup>-5</sup> mol/L. The reduction mechanism of ECAB and RE-ECAB is proposed based on the experimental evidence. The complexing group of ECAB with RE ions iust is the redox group, so when RE ions are added, there is no new peak appearing in the polarograms:, the only phenomenon observed is that the peak current of ECAB decreases. The fast protonation of EGAB carbanion formed after the second electron transfer results in the formation of colourless tetrahedral molecules.
