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Standardization for trace metal ion speciation by the electrochemical

Standardization for trace metal ion speciation by the electrochemical
通过电化学方法对痕量金属离子形态进行标准化
批准号:
10640592
负责人:
YOKOI Kunihiko
金额:
$2.11万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1998
资助国家:
日本
项目状态:
已结题
起止时间:
1998 至 1999

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中文摘要
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英文摘要
To establish the procedure of the standardization for trace metal ion speciation, fundamental data, such as complexing capacity(CC) and the conditional stability constants(K'), for the interaction of metal ion (copper and nickel) and humas(humic(HA) and fulvic acids(FA)) were collected. HA and FA were prepared as standard materials by The Japan Society for Humic Substances. CC and K' were estimated from metal ion titration by adsorptive stripping voltammetry. Quinoline-8-ol(OX) and dimethylglyoxime(DMG) were used as complexing ligands for copper and nickel, respectively. As the increase of the concentration of OX and DMG, CuCC and NiCC for HA and FA were decreased while K's were increased. This indicates the presence of various coordination sites having different coordination ability, because HA and FA are the mixture of organic compounds having various functional groups and large molecular weights. The relative values for CuCC(HA), NiCC(HA), CuCC(FA) and NiCC(FA) were ca. 450, 30, 30 … More and 1, respectively. To explain these results based on chemical equilibria, three coordination groups, having different number of sites(that is,CC) and K', were assumed. And then, the simulated metal ion titration curve were analyzed by the normal procedure for obtaining CC and K' based on the assumption that one metal ion reacts with one coordination site. This calculation was repeated for different initial CC and K' for assumed coordination sites till the calculated CC and K' were within the range of observed values. For the interactions of Cu-HA, Ni-HA, Cu-FA, good agreement was obtained between observed and calculated values. This enabled us to discuss about the distribution of coordination sites in HA and FA. Additional projects for speciation were also carried out on popularization of the concept of speciation, contamination-free pre-treatment of water samples by UV irradiation with high output low-pressure mercury lamp, electrochemical ultra trace analysis using catalytic effect, synthesis of multidentate ligands to specaiate lanthanide ions and their application to solvent extraction, and production of big wheel mixed-valence compounds to speciate giant molecules. Novel results were also obtained for these projects. Less
期刊论文(36)
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会议论文
久保埜 公二: "平面型Schiff塩基系配位子によるCe(IV)錯体の構造"日本化学会第78春季年会講演要旨集. (掲載予定). (2000)
Koji Kubota:“Ce(IV) 配合物与平面席夫碱配体的结构”第 78 届日本化学会春季年会论文集(待出版)。
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通讯作者:
Koji Kubono: "Solvent extraction of metal ions by simultaneous using of two kinds of multidentate ligands"Abstract of 59th spring meeting of The Japan Society for Analytical Chemistry. 175 (1998)
Koji Kubono:“同时使用两种多齿配体的金属离子溶剂萃取”日本分析化学学会第 59 届春季会议摘要。
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Koji Kubono: "Extractive separation of lanthnoides by simultaneous using of two kinds of multidentate ligands"Abstract of 47th annual meeting of The Japan Society for Analytical Chemistry. 337 (1998)
Koji Kubono:“通过同时使用两种多齿配体对镧系元素进行提取分离”日本分析化学学会第 47 届年会摘要。
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横井邦彦: "吸着濃縮ボルタンメトリーによるフミン酸標準試料の銅及びニッケル錯化容量と条件安定度定数の見積もり"日本分析化学会第48年会講演要旨集. 300 (1999)
Kunihiko Yokoi:“通过吸附浓度伏安法估算腐殖酸标准样品的铜和镍络合能力和条件稳定性常数”日本分析化学学会第48届年会记录300(1999)。
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35
    Development of an ultra-sensitive electrochemical method for the determination of phosphate ion with molecular fractionation and adsorptive collection
    • 批准号:
      13640606
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.24万
    • 财政年份:
      2001
    • 负责人:
      YOKOI Kunihiko
    • 依托单位:
    Development of the method for environmental assessments based on the recognition of the correlation between the speciation of trace metals and the response by living organisms
    • 批准号:
      06640785
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $1.41万
    • 财政年份:
      1994
    • 负责人:
      YOKOI Kunihiko
    • 依托单位:
    海外基金