Bulletin of the Society of Sea Water Science, Japan
Online ISSN : 2185-9213
Print ISSN : 0369-4550
ISSN-L : 0369-4550
Volume 64, Issue 3
Displaying 1-6 of 6 articles from this issue
Greeting
Report on The 1st Student Meeting
Preprints of The 61th Annual Meeting
Original Paper
  • Tomoya Yamamoto, Kentaro Miyawaki, Osamu Itoh, Yoshifumi Akama
    2010 Volume 64 Issue 3 Pages 170-176
    Published: May 20, 2010
    Released on J-STAGE: July 21, 2011
    JOURNAL FREE ACCESS
    A new chemically modified cellulose (Cell-NMG) with N-methyl glycin was prepared and used as a solid-phase extractant for the simultaneous extraction of trace Cu2+, Ni2+ and Co2+ prior to their determination by flame AAS. The Cell-NMG and metal-adsorbed Cell-NMG — metal were characterized by FT-IR and thermal analysis.
    The effect of various parameters such as acidity, eluting solution, shaking time, flow rate, sample volume, interfering cations, etc., have been studied in detail. The quantitative adsorption for Cu2+ was at pH>4.8, for Ni2+ at pH>5.5 and for Co2+ at pH>6.1. For simultaneous enrichment of all the metal ions on the adsorbent, a pH value on about 6.5 was selected. The retention of the metal ions on the adsorbent was not influenced by the sample flow-rate within the studied range of 5∼25 mL/min. A flow rate of 15 mL/min was selected for adsorption, and the retained metal ions on the microcolumn (polypropyrene syringe, 78×15 mm i.d., 1.0 g of Cell-N-MG was packed) were eluted with 10 mL of 1.0 mol/L HCl solution at a flow rate of 7 mL/min. The maximum sorption capacities were found to be 0.38 mmol/g for Cu2+, 0.27 mmol/g for Ni2+ and 0.25 mmol/g for Co2+. This method has been successfully applied to study the recovery of the metal ions in spiked ground water, river water and cooking salt samples.
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