• 제목/요약/키워드: polyanions

검색결과 3건 처리시간 0.015초

몰리브덴의 용액화학 (Aqueous Chemistry of Molybdenum)

  • 이만승;최승훈
    • 자원리싸이클링
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    • 제27권4호
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    • pp.44-49
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    • 2018
  • 몰리브덴은 알칼리용액에서는 $MoO{_4}^{2-}$로 존재한다. 수용액의 pH 2와 6 사이의 범위에서는 $MoO{_4}^{2-}$와 수소이온간의 축중합반응에 의해 다양한 동종다중음이온이 형성된다. 몰리브덴용액의 pH가 2 이하의 범위에서는 동종다중양이온이 형성되나 무기산의 농도가 증가함에 따라 무기산의 음이온과 반응하여 이종다중음이온이 형성된다. pH 6 이하의 용액에서 몰리브덴의 농도분포는 몰리브덴과 무기산의 종류와 농도에 의존한다. 따라서 용매추출과 이온교환자료를 해석하기 위해서는 강산용액에서 몰리브덴 화학종을 규명할 필요가 있다.

Optimization of Synthetic Parameters for Mesoporous Molecular Sieve MCM-41 Using Surfactant CTAC1

  • 박동호;Cheng, Chi Feng;Jacek Klinowski
    • Bulletin of the Korean Chemical Society
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    • 제18권4호
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    • pp.379-384
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    • 1997
  • High quality MCM-41 is prepared from a gel of molar composition SiO2:0.20 CTACl:0.18 TMAOH:25 H2O aged at 20 ℃ for 24 hours before crystallization lasting for 48 hours. The (110) and (200) peaks of XRD pattern of high quality MCM-41 are unusually well resolved and the FWHM (full-width-at-half-maximum) of the (100) peak is 0.13° for as-prepared MCM-41 and 0.21° for calcined one, which indicate well-developed crystals. The properties of the crystal depend on the source and concentration of the reactants and the gel aging time. There is no induction period in the course of the synthesis, which is conveniently monitored by pH measurement. Gel aging, during which a spatial distribution of silicate polyanions and micellar cations is established, is essential for preparing high quality MCM-41. Surfactants with the same cationic organic group but different counteranions change the crystallization behavior. Highly basic gel (pH=12.6) favours the lamellar product; the quality of MCM-41 is lower as insufficient TMAOH is available to dissolve the silica.

Effects of Polyelectrolytes on the Charge Transfer Complexing between Indole derivatives and Methylviologen: Hydrophobic and Electrostatic Interactions

  • Park, Joon-Woo;Hwang, Book-Kee
    • Bulletin of the Korean Chemical Society
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    • 제6권3호
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    • pp.145-148
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    • 1985
  • The effect of anionic polyelectrolytes, poly(styrenesulfonate) (PSS) and poly(vinylsulfonate) (PVS), on the charge transfer complexing between indole derivatives and methyl viologen($MV^{++}$) cation was investigated. The results were compared with effect of NaCl and an anionic surfactant, sodium dodecylsulfate (SDS). Both PSS and PVS enhanced the complex formation of neutral species (indole and indole acetate at low pH), zwitter ionic tryptophan, and positively charged tryptamine and tryptophan at low pH with $MV^{++}$. This result was attributed to the contribution of hydrophobic interaction, in addition to electrostatic interaction. The enhancing effect of PSS was much higher than that of PVS reflecting the higher hydrophobicity of PSS. The interaction between indole acetate anion and $MV^{++}$ was greatly reduced by addition of PVS and PSS. The higher charge density of PVS was appeared as greater reducing effect indicating the importance of electrostatic force in this case. In all cases, the effect of polyelectrolytes showed maxima, and further addition of PVS and PSS decreased the effect. This behavior was explained in terms of distribution of indole derivatives and $MV^{++}$ in domain of polyanions. The complex formation constants and molar absorptivities of complexes were determined, and the values were compared with those in water and SDS solutions.