Adsorption Mechanism of Solid Acid in Nonaqueous Solution

固體酸의 非水溶液에서의 吸着메카니즘에 관한 硏究

  • 권오천 (漢陽大學校 文理科大學 化學科)
  • Published : 19651200

Abstract

Korean acid clays and silica gel were put into action on benzene solution of dye, such as aniline yellow, o-nitro aniline and oil orange, and then the adsorptivity of dye in nonaqueous solution was measured, with the result that adsorptivity was greater with silica than acid clays and it had no relation to acidity. And when chemical compounds, such as amine, alcohol, halogen derivative, were added to each dye solution by 10%(in volume), the change of the adsorptivity of dye by solid acid(that is, the interfered adsorption rate) decreased in order of amine > alcohol > halogen derivative, and in homologue the smaller the molecular weight, the larger was the effect. So adsorption in nonaqueous solution was a selective adsorption of chemical compounds which contained negative groups such as amine and hydroxyl radicals, and it had no relation to surface tension and showed inverted phenomenon of Traube series. It is guessed that the inverted phenomenon (the interfered adsorption phenomenon) was due to the polar chemical adsorption between active $SiO_2$ which was an origin of solid acid and the adsorbed substances, considering that the order of inversion was nearly in accord with dipole moment of added solvents. The results of this study led to find adsorption mechanism and inverted phenomenon of Traube series in nonaqueous solution.

韓國産 酸性白土類 및 silica gel을 aniline yellow, o-nitro aniline, oil orange 色素 benzene 溶液과 작용시켜 非水溶液에서의 色素吸着率을 측정하였다. 그 吸着率은 silica gel이 酸性白土類보다 컸으며 酸性度에는 무관하였다. 또 上記 色素溶液에 각 10%의 添加溶劑 amine, alcohol, halogen類 化合物등을 加하여 高體酸의 色素吸着率의 변화(吸着阻害率)에 대하여 조사한 결과 위에 적은 順으로 그 영향이 적어지고, 同族體에서는 分子量이 적을 수록 그 영향이 커짐을 알았다. 따라서 非水溶液에서의 吸着은 amine基, 水酸基등과 같은 陰性基를 갖는 化合物은 選擇吸着하고 界面張力에 무관계하여 Traulbe系列의 逆轉現象을 나타내었다. 그 逆轉現象(吸着潮害現象)은 그 順位가 添加溶制의 雙極子能率과 대체적으로 일치하는 것으로 보아 固體酸模體인 活性硅酸과 被吸着體사이의 極盛的化學吸着에 의한 것이라 推定된다. 本實驗結果로부터 固體酸의 非水溶液에서의 吸着메카니즘, Traube 系列의 逆轉現象에 관하여 考察하게 되었다.

Keywords

References

  1. Journal of the Korean Chemical Society v.9 權五千
  2. Z. Angew. Chem. v.40 B. Neumann;U. S. Kober
  3. J. Phys. Chem. v.18 F.B. Bartell;E.J. Miller
  4. J. Phys. Chem. v.30 E.J. Miller
  5. J. Phys. Chem. v.31 E.J. Miller
  6. Petrol. Z. v.24 O. Eckart
  7. Kogyo Kagaku Zasshi. v.33 小林久平;山本硏一
  8. Kogyo Kagaku Zasshi. v.32 田中芳雄;桑田勉
  9. Kogyo Kagaku Zasshi. v.35 田中芳雄;桑田勉
  10. Kapillar Chem. v.1 H. Freundlich
  11. Bull. Chem. Soc., Japan v.7 玉蟲文一
  12. J. Ind. Chem. Soc. v.16 S.S. Bhatnager;A.N. Kapur;M.S. Bhatnager
  13. J. Ind. Chem. Soc. v.16 S.S. Bhatnager;A.N. Kapur;Makendra
  14. J. Ind. Chem. Soc. v.13 S.S. Bhatnager;A.N. Kapur;M.L. Puri
  15. J. Ind. Chem. Soc. v.17 S.S. Bhatnager;A.N. Kapur;M.S. Bhatnager
  16. Kogyo Kagaku Zasshi. v.41 鶴田四郞
  17. 分子構造論 基礎 東健一
  18. Ind. Eng. Chem., Anal. Ed. v.5 R.T. Morse