Journal of Ion Exchange
Online ISSN : 1884-3360
Print ISSN : 0915-860X
ISSN-L : 0915-860X
Volume 11, Issue 2
Displaying 1-4 of 4 articles from this issue
  • Sang-Ho KIM, Masao AIDA, Masao NOMURA, Rifaid M. NUR, Yasuhiko FUJII
    2000Volume 11Issue 2 Pages 26-31
    Published: September 20, 2000
    Released on J-STAGE: March 18, 2010
    JOURNAL FREE ACCESS
    Isotope effects of iron in Fe (II) -Fe (III) electron exchange system were studied using anion exchange chromatography. It was found that the heavier isotope is enriched at the rear part of the iron adsorption band. The results indicate that the heavier isotope is preferentially fractionated in Fe (III) chloride complex ions in the anion exchange resin phase. The single stage separation coefficient, ε, observed for 57Fe/56Fe isotopic pair was 2.06×10-4 at 333 K. The height equivalent to theoretical plate was calculated to be 0.68mm.
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  • Hiromichi HAYASHI, Yoshio ONODERA, Takashi IWASAKI
    2000Volume 11Issue 2 Pages 32-39
    Published: September 20, 2000
    Released on J-STAGE: March 18, 2010
    JOURNAL FREE ACCESS
    Intercalation of (3-aminopropyl) triethoxysilane, AMPS, into cerium (IV) hydrogenphosphate (CeP) was investigated by X-ray diffractometry, chemical and thermal analysis, 29Si MAS NMR, and FTIR. AMPS intercalated up to 1.2 mol per phosphate accompanied by hydrolysis of the ethoxy groups and the interlayer spacing of the CeP enlarged from 1.1nm to 1.7nm. The 29Si MAS NMR spectra revealed that the AMPS undergoes polymerization and AMPS octamer, [NH2 (CH2) 3SiO1.5-O (OH) Si (CH2) 3NH2] 4, is formed in the interlayer space of CeP. Infrared spectra showed that the aminopropyl group exists as an ammonium form. On the basis of the relation between the uptake of metal ions and the leached amount of AMPS, the intercalated AMPS octamers was found to be exchanged with divalent metal cations stoichiometrically. Selectivity for the divalent metal ions increases with the following order; Ca2+>Sr2+>Ba2+>Cu2+>Co2+>Ni2+. This order agrees with that of the octylamine-intercalated CeP.
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  • Mutsuyoshi KITAMOTO
    2000Volume 11Issue 2 Pages 40-44
    Published: September 20, 2000
    Released on J-STAGE: March 18, 2010
    JOURNAL FREE ACCESS
    wide varieties of Ion Exchange Resins are commercially produced at present. Their fundamental polymer structures are classified into gel type and macro-porous type from the point of physical structure. In this paper, I will brief on the preparation methods for macro-porous structure and their features of each preparation approach.
    I will also touch on recent commercial resins having unique macro-porous structure.
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  • Kyoichi SAITO
    2000Volume 11Issue 2 Pages 45-52
    Published: September 20, 2000
    Released on J-STAGE: March 18, 2010
    JOURNAL FREE ACCESS
    Development of novel ion-exchange resins is continuing to improve their performance of ionexchange rate, capacity, and durability. For example, porous ion-exchange resins of a hollowfiber membrane form were prepared by radiation-induced grafting of polymer brushes and subsequent chemical modifications. The ion-exchange resins exhibited a higher rate and capacity for protein capturing than conventional ion-exchange beads because of convective transport of the protein through the pores and multilayer binding of the protein to the ion-exchange polymer brushes.
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