浮選分離-還元気化原子吸光法による海水中のヒ素の定量

書誌事項

タイトル別名
  • 浮選分離‐還元気化原子吸光法による海水中のひ素の定量
  • Atomic absorptiometric determination of arsenic in sea water by hydride generation after separating by flotation
  • フセン ブンリ カンゲン キカ ゲンシ キュウコウホウ ニヨル カイスイチュウ

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抄録

A rapid and precise method is described for the separation and determination of arsenic in natural sea water. The procedure is as follows: Add 2 ml of iron (III) solution (5 mg ml-1) to 250 ml of sea water in a 300-ml beaker. Adjust the pH to 89with aqueous ammonia solution, and stir the solution for 15 min. After adding 1 ml of sodium oleateethanol solution (1 mg ml-1), transfer the contents of the beaker to a flotation cell (24×4.8 cm i.d.) fitted with a sintered-glass filter (No.4). Pass air at 50 ml min-1 from the lower end of the cell about 1 min. Suck off the mother liquor through the sinteredglass disk. Add 5 M hydrochloric acid to dissolve the precipitate, collect the filtrate by suction in a 10-ml calibrated flask and dilute to 9 ml. Add 0.5 ml of 20% (w/v) potassium iodide solution into the flask prior to analysis and dilute to the mark with water. Transfer 1 ml of 5 % (w/v) sodium borohydride solution into a hydride generating cell. Inject 1 ml of sample solution containing less than 0.10 μg of arsenic into the cell. Sweep the arsine thus generated into the long absorption cell (60×1.2 cm i.d.) with nitrogen so that it is atomized in the nitrogen-hydrogen flame and measure the absorption signal of arsenic by atomic absorption spectrophotometry. The potassium iodide pretreatment after the separation eliminated suppressive effects by diverse ions such as Cu2+, Se4+ and Ni2+ in the determination of arsenic. In the analytical process, mean recoveries were (99101) % for arsenic (III, V) added to natural sea waters. The relative standard deviations of 7 replicate analyses of sea water samples were less than 3%.

収録刊行物

  • 分析化学

    分析化学 28 (9), 561-563, 1979

    公益社団法人 日本分析化学会

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