2002
DOI: 10.1007/bf02492321
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Application of pure silica gel as cation-exchange stationary phase in lon chromatography with indirect photometric detection for common mono-and divalent cations using aromatic monoamines as eluents

Abstract: SummaryA pure silica gel (Pia Seed 5S-60-SIL), synthesized by the hydrolysis of pure tetraethoxysilane [Si(OCH2CH3)4L was applied as a cation-exchange stationary phase in ion chromatography with indirect photometric detection for common mono-and divalent cations (Li +, Na +, NH4 +, K +, Mg 2+ and Ca 2+) using various protonated aromatic monoamines (tyramine [4-(2-aminethyl)phenolL benzylamine, phenylethylamine, 2-methylpyridine and 2,6-dimethylpyridine) as eluent ions. When using 0.75 mM tyramine-0.25 mM oxali… Show more

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Cited by 9 publications
(4 citation statements)
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“…Ionizable molecules that are to be purified compete with these counterions for binding to the immobilized charges on the stationary phase. These ionizable molecules are retained based on their charges 11,13 .…”
Section: Ion-exchange Chromatographymentioning
confidence: 99%
“…Ionizable molecules that are to be purified compete with these counterions for binding to the immobilized charges on the stationary phase. These ionizable molecules are retained based on their charges 11,13 .…”
Section: Ion-exchange Chromatographymentioning
confidence: 99%
“…WCX (the majority functional groups of WCX are carboxylate groups) is superior to strong cation exchanger since hydronium has stronger affinity with WCX relative to strong cation exchanger, then leading to strong elution ability toward metal cations. Bare silica itself can serve as a WCX since its surface is negatively charged owing to the dissociation of silanol groups [7]. The main drawbacks of bare silica as WCX are limited capacity and selectivity.…”
Section: Introductionmentioning
confidence: 99%
“…Zhang et al (2006) characterized of phenol-liquefied triploid clones of Populus tomentosa and Cunninghamia lanceolata by Fourier transform infrared spectroscopy (FTIR), 1 H NMR, 13 C NMR, 31 P NMR and scanning electron microscope (SEM). During separation, the polarity of the eluent must be very sensitive in order to optimize the separation of compounds (Ohta et al, 2002). And the sorbent, the polarity of mobile phase and the sample must all be considered in this process (Stella et al, 2001;Cebolla et al, 2002).…”
Section: Introductionmentioning
confidence: 99%