The Experts below are selected from a list of 79443 Experts worldwide ranked by ideXlab platform

Soo Beng. Khoo - One of the best experts on this subject based on the ideXlab platform.

Mayakrishnan Prabakaran - One of the best experts on this subject based on the ideXlab platform.

I-wen Sun - One of the best experts on this subject based on the ideXlab platform.

  • cathodic stripping voltammetric determination of selenium iv at a nafion coated mercury film electrode modified with 3 3 Diaminobenzidine
    Electroanalysis, 2000
    Co-Authors: Hao Yun Yang, I-wen Sun
    Abstract:

    Determination of selenium(IV) was investigated on a 3,3′-Diaminobenzidine/Nafion/mercury film modified glassy carbon electrode (DNMFE). The 3,3′-Diaminobenzidine/Nafion coating solution was irradiated by a tungsten light bulb to oxidize the 3,3′-Diaminobenzidine. This coating solution was then spin-coated onto a glassy carbon electrode. Subsequently, mercury was electrodeposited onto the electrode surface. Selenium(IV) was preconcentrated onto the DNMFE from the sample solution saturated with ethylenediaminetetraacetate (EDTA) at an accumulation potential of –0.35 V, and determined by cathodic square-wave stripping voltammetry (SWSV). Various parameters affecting the selenium determination were examined. With 5 min accumulation, the analytical signal was linear from 1 to 300 µgL–1, and the detection limit was 0.48 µgL–1. The proposed procedure showed a good accumulation efficiency for selenium and good resistance to interferences from metal ions as well as surface-active compounds.

  • Determination of selenium(IV) by a photooxidized 3,3'-Diaminobenzidine/perfluorinated polymer mercury film electrode
    Analytical chemistry, 2000
    Co-Authors: Hao Yun Yang, I-wen Sun
    Abstract:

    A new, and easily fabricated, chemically modified electrode for the determination of selenium(IV) was examined by cathodic square-wave stripping voltammetry. This new electrode consisted of an anion-exchange perfluorinated polymer (Tosflex) coated thin mercury film electrode containing photooxidized 3,3'-Diaminobenzidine (ODAB). The coating solution of Tosflex and ODAB was spin-coated on a glassy carbon electrode followed by electroplating of a thin film of mercury. During the preconcentration, ODAB was reduced electrochemically and selenium was accumulated simultaneously onto the electrode by interacting with the reduced ODAB. After a 5-min preconcentration period, linear response was observed from 0.5 to 50 ppb selenium, and the detection limit was 0.1 ppb. The proposed method does not require a darkened room, which was required in many of the previous methods involving 3,3'-Diaminobenzidine. In addition, the resistance to interference from surface-active compounds was improved by incorporating Tosflex in the film.

  • determination of selenium iv by a photooxidized 3 3 Diaminobenzidine perfluorinated polymer mercury film electrode
    Analytical Chemistry, 2000
    Co-Authors: Hao Yun Yang, I-wen Sun
    Abstract:

    A new, and easily fabricated, chemically modified electrode for the determination of selenium(IV) was examined by cathodic square-wave stripping voltammetry. This new electrode consisted of an anion-exchange perfluorinated polymer (Tosflex) coated thin mercury film electrode containing photooxidized 3,3'-Diaminobenzidine (ODAB). The coating solution of Tosflex and ODAB was spin-coated on a glassy carbon electrode followed by electroplating of a thin film of mercury. During the preconcentration, ODAB was reduced electrochemically and selenium was accumulated simultaneously onto the electrode by interacting with the reduced ODAB. After a 5-min preconcentration period, linear response was observed from 0.5 to 50 ppb selenium, and the detection limit was 0.1 ppb. The proposed method does not require a darkened room, which was required in many of the previous methods involving 3,3'-Diaminobenzidine. In addition, the resistance to interference from surface-active compounds was improved by incorporating Tosflex in the film.

  • Cathodic stripping voltammetric determination of selenium(IV) at a nafion coated mercury film electrode modified with 3,3′-Diaminobenzidine
    Electroanalysis, 2000
    Co-Authors: Hao Yun Yang, I-wen Sun
    Abstract:

    Determination of selenium(IV) was investigated on a 3,3′-Diaminobenzidine/Nafion/mercury film modified glassy carbon electrode (DNMFE). The 3,3′-Diaminobenzidine/Nafion coating solution was irradiated by a tungsten light bulb to oxidize the 3,3′-Diaminobenzidine. This coating solution was then spin-coated onto a glassy carbon electrode. Subsequently, mercury was electrodeposited onto the electrode surface. Selenium(IV) was preconcentrated onto the DNMFE from the sample solution saturated with ethylenediaminetetraacetate (EDTA) at an accumulation potential of –0.35 V, and determined by cathodic square-wave stripping voltammetry (SWSV). Various parameters affecting the selenium determination were examined. With 5 min accumulation, the analytical signal was linear from 1 to 300 µgL–1, and the detection limit was 0.48 µgL–1. The proposed procedure showed a good accumulation efficiency for selenium and good resistance to interferences from metal ions as well as surface-active compounds.

Venkittapuram Palaniswamy Radha - One of the best experts on this subject based on the ideXlab platform.

Hao Yun Yang - One of the best experts on this subject based on the ideXlab platform.

  • cathodic stripping voltammetric determination of selenium iv at a nafion coated mercury film electrode modified with 3 3 Diaminobenzidine
    Electroanalysis, 2000
    Co-Authors: Hao Yun Yang, I-wen Sun
    Abstract:

    Determination of selenium(IV) was investigated on a 3,3′-Diaminobenzidine/Nafion/mercury film modified glassy carbon electrode (DNMFE). The 3,3′-Diaminobenzidine/Nafion coating solution was irradiated by a tungsten light bulb to oxidize the 3,3′-Diaminobenzidine. This coating solution was then spin-coated onto a glassy carbon electrode. Subsequently, mercury was electrodeposited onto the electrode surface. Selenium(IV) was preconcentrated onto the DNMFE from the sample solution saturated with ethylenediaminetetraacetate (EDTA) at an accumulation potential of –0.35 V, and determined by cathodic square-wave stripping voltammetry (SWSV). Various parameters affecting the selenium determination were examined. With 5 min accumulation, the analytical signal was linear from 1 to 300 µgL–1, and the detection limit was 0.48 µgL–1. The proposed procedure showed a good accumulation efficiency for selenium and good resistance to interferences from metal ions as well as surface-active compounds.

  • Determination of selenium(IV) by a photooxidized 3,3'-Diaminobenzidine/perfluorinated polymer mercury film electrode
    Analytical chemistry, 2000
    Co-Authors: Hao Yun Yang, I-wen Sun
    Abstract:

    A new, and easily fabricated, chemically modified electrode for the determination of selenium(IV) was examined by cathodic square-wave stripping voltammetry. This new electrode consisted of an anion-exchange perfluorinated polymer (Tosflex) coated thin mercury film electrode containing photooxidized 3,3'-Diaminobenzidine (ODAB). The coating solution of Tosflex and ODAB was spin-coated on a glassy carbon electrode followed by electroplating of a thin film of mercury. During the preconcentration, ODAB was reduced electrochemically and selenium was accumulated simultaneously onto the electrode by interacting with the reduced ODAB. After a 5-min preconcentration period, linear response was observed from 0.5 to 50 ppb selenium, and the detection limit was 0.1 ppb. The proposed method does not require a darkened room, which was required in many of the previous methods involving 3,3'-Diaminobenzidine. In addition, the resistance to interference from surface-active compounds was improved by incorporating Tosflex in the film.

  • determination of selenium iv by a photooxidized 3 3 Diaminobenzidine perfluorinated polymer mercury film electrode
    Analytical Chemistry, 2000
    Co-Authors: Hao Yun Yang, I-wen Sun
    Abstract:

    A new, and easily fabricated, chemically modified electrode for the determination of selenium(IV) was examined by cathodic square-wave stripping voltammetry. This new electrode consisted of an anion-exchange perfluorinated polymer (Tosflex) coated thin mercury film electrode containing photooxidized 3,3'-Diaminobenzidine (ODAB). The coating solution of Tosflex and ODAB was spin-coated on a glassy carbon electrode followed by electroplating of a thin film of mercury. During the preconcentration, ODAB was reduced electrochemically and selenium was accumulated simultaneously onto the electrode by interacting with the reduced ODAB. After a 5-min preconcentration period, linear response was observed from 0.5 to 50 ppb selenium, and the detection limit was 0.1 ppb. The proposed method does not require a darkened room, which was required in many of the previous methods involving 3,3'-Diaminobenzidine. In addition, the resistance to interference from surface-active compounds was improved by incorporating Tosflex in the film.

  • Cathodic stripping voltammetric determination of selenium(IV) at a nafion coated mercury film electrode modified with 3,3′-Diaminobenzidine
    Electroanalysis, 2000
    Co-Authors: Hao Yun Yang, I-wen Sun
    Abstract:

    Determination of selenium(IV) was investigated on a 3,3′-Diaminobenzidine/Nafion/mercury film modified glassy carbon electrode (DNMFE). The 3,3′-Diaminobenzidine/Nafion coating solution was irradiated by a tungsten light bulb to oxidize the 3,3′-Diaminobenzidine. This coating solution was then spin-coated onto a glassy carbon electrode. Subsequently, mercury was electrodeposited onto the electrode surface. Selenium(IV) was preconcentrated onto the DNMFE from the sample solution saturated with ethylenediaminetetraacetate (EDTA) at an accumulation potential of –0.35 V, and determined by cathodic square-wave stripping voltammetry (SWSV). Various parameters affecting the selenium determination were examined. With 5 min accumulation, the analytical signal was linear from 1 to 300 µgL–1, and the detection limit was 0.48 µgL–1. The proposed procedure showed a good accumulation efficiency for selenium and good resistance to interferences from metal ions as well as surface-active compounds.