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Determination of the Activity of Hydrogen Ions in Dilute Sulfuric Acids by Use of an Ionic Liquid Salt Bridge Sandwiched by Two Hydrogen Electrodes

机译:用两个氢电极夹心的离子液体盐桥测定稀硫酸中的氢离子活性

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摘要

The activities of hydrogen ions in 20 200 µmol dm 3nH2SO4 solution were estimated by use of an ionicnliquid salt bridge (ILSB), made of tributyl(2-meth-noxyethyl)phosphonium bis(pentafluoroethanesulfo-nnyl)amide (TBMOEPC2C2N), sandwiched by twonhydrogen electrodes. The experimental pH valuesn(pH log aH, where aH is the activity of hydrogennions) were in good agreement, within 0.01 pH unit,nwith those calculated using the Pitzer model. Thendifference between the experimental and theoreticalnpH values at 50 µmol dm 3 H2SO4 solution wasnmuch smaller than that obtained by use of a glassnelectrode in combination with a reference electrodenwith a concentrated KCl salt bridge. The sourcenof the small deviation can be explained by the resi-ndual diffusion potential due to the dissolution ofnTBMOEPC2C2N in the H2SO4 solution (W) and thenresultant increase in the ionic strength of W. The usenof a reference electrode equipped with an ILSBnopens the way to accurately estimate the pH in dilutenaqueous solutions, for which we have not had effec-ntive means.
机译:通过使用离子液体盐桥(ILSB)估算20 200 µmol dm 3nH2SO4溶液中氢离子的活性,该离子桥由三丁基(2-甲基-氧乙基)phosph双(五氟乙烷磺酰基-丙烯基)酰胺(TBMOEPC2C2N)制成电极。实验的pH值n(pH log aH,其中aH是氢离子的活性)与0.01的pH值相吻合,与使用Pitzer模型计算得到的值相吻合。在50 µmol dm 3的H2SO4溶液中,实验pH值与理论pH值之间的差异远小于将玻璃电极与带有浓KCl盐桥的参比电极组合使用所获得的pH值。小偏差的来源可以由nTBMOEPC2C2N在H2SO4溶液(W)中的溶解所导致的剩余扩散电位来解释,然后导致W的离子强度增加。使用配备有ILSBn的参比电极为准确地开辟道路估计稀释溶液中的pH,而我们还没有有效的手段。

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  • 来源
    《Analytical Chemistry》 |2011年第1期|p.164-168|共5页
  • 作者单位

    R&D Center, Horiba, Ltd., Kyoto 601-8510, Japan, and Department of Energy and Hydrocarbon Chemistry, GraduateSchool of Engineering, Kyoto University, Kyoto 615-8510, Japan;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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