Kinetic and spectral studies of EHPG systems using chemi-and electrochemiluminescence methods  

Kinetic and spectral studies of EHPG systems using chemi-and electrochemiluminescence methods

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作  者:S. Lis M. Kaczmarek K. Staninski S. Krompiec N. Kuznik 

机构地区:[1]Faculty of Chemistry, Adam Mickiewicz University [2]Institute of Chemistry, University of Silesia [3]Faculty of Chemistry, Silesian Technical University

出  处:《Journal of Rare Earths》2010年第6期868-873,共6页稀土学报(英文版)

基  金:Project supported by the grants of Polish Ministry of Science and Higher Education nr N N204 028236 and partly nr N N204 030935

摘  要:The systems containing EHPG, EHPG-OCH3 and EHPG-NH-Ac and Tb(Ⅲ) ions were used to study chemiluminescence (CL) and electrochemiluminescence (ECL) processes. In the CL studies the Fenton system (Fe(Ⅱ)/(Ⅲ)-H2O2) was used as a source of reactive oxygen species (ROS). Kinetic CL curves and CL spectral distributions were recorded. On the basis of the results obtained, it was demonstrated that Tb(Ⅲ) acted as a sensitizer. Similarly obtained CL decays in the systems of Fe(Ⅱ)/(Ⅲ)-EHPG (or its derivatives)-H2O2 and Fe(Ⅱ)/(Ⅲ)-EHPG (or its derivatives)-Tb(Ⅲ)-H2O2, independently on the Tb(Ⅲ) concentration, showed that the lanthanide ions did not influence the kinetics of the oxidation of EHPG (or its derivatives) in the Fenton systems. The CL intensity increased with the increasing concentration of Tb(Ⅲ) ions, which were the main emitters in the reaction systems. Spectrophotometric and luminescent studies of the systems before and after the additions of hydrogen peroxide proved that the excitation of the lanthanide ion was a result of energy transfer from the excited products of the oxidation of EHPG or its derivatives to the uncomplexed Tb(Ⅲ) ions. ECL was generated on the surface of a nonstructural modified aluminum electrode with the use of K2S2O8, H2O2 or KN3 as coreactants in aqueous solution. In these studies we employed Al electrodes covered with a 2-4 nm layer of Al2O3 doted with Tb(Ⅲ) or Dy(Ⅲ) ions. The electrodes were polarized using cathodic and anodic pulses of various amplitude and frequency. The relative ECL efficiencies were determined as a function of electric pulse parameters, electrolyte compositions and the thickness of barrier or porous layer of the Al2O3 electrode.The systems containing EHPG, EHPG-OCH3 and EHPG-NH-Ac and Tb(Ⅲ) ions were used to study chemiluminescence (CL) and electrochemiluminescence (ECL) processes. In the CL studies the Fenton system (Fe(Ⅱ)/(Ⅲ)-H2O2) was used as a source of reactive oxygen species (ROS). Kinetic CL curves and CL spectral distributions were recorded. On the basis of the results obtained, it was demonstrated that Tb(Ⅲ) acted as a sensitizer. Similarly obtained CL decays in the systems of Fe(Ⅱ)/(Ⅲ)-EHPG (or its derivatives)-H2O2 and Fe(Ⅱ)/(Ⅲ)-EHPG (or its derivatives)-Tb(Ⅲ)-H2O2, independently on the Tb(Ⅲ) concentration, showed that the lanthanide ions did not influence the kinetics of the oxidation of EHPG (or its derivatives) in the Fenton systems. The CL intensity increased with the increasing concentration of Tb(Ⅲ) ions, which were the main emitters in the reaction systems. Spectrophotometric and luminescent studies of the systems before and after the additions of hydrogen peroxide proved that the excitation of the lanthanide ion was a result of energy transfer from the excited products of the oxidation of EHPG or its derivatives to the uncomplexed Tb(Ⅲ) ions. ECL was generated on the surface of a nonstructural modified aluminum electrode with the use of K2S2O8, H2O2 or KN3 as coreactants in aqueous solution. In these studies we employed Al electrodes covered with a 2-4 nm layer of Al2O3 doted with Tb(Ⅲ) or Dy(Ⅲ) ions. The electrodes were polarized using cathodic and anodic pulses of various amplitude and frequency. The relative ECL efficiencies were determined as a function of electric pulse parameters, electrolyte compositions and the thickness of barrier or porous layer of the Al2O3 electrode.

关 键 词:CHEMILUMINESCENCE LANTHANIDES EHPG complexes rare earths 

分 类 号:O614.33[理学—无机化学]

 

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