2014
DOI: 10.2116/analsci.30.51
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Diverse Secondary Interactions between Ions Exchanged into the Resin Phase and Their Analytical Applications

Abstract: The research activities by the author's group to elucidate the chemical states of ions within the ion exchange resin phase are summarized. The resin with the higher exchange capacity has the smaller space available for ion exchange, and the higher cross linking degree interferes more with swelling of the resin. As a result, diverse secondary interactions between exchanged ions are observed on the resins of high exchange capacities and high cross linking degrees: the van der Waals contact results in incomplete … Show more

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Cited by 10 publications
(3 citation statements)
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“…Kinetic and equilibrium adsorption measurements have essential role to get information for the design and operation of phosphate removal process in water/wastewater treatment (Yuchi, 2014).…”
Section: Kinetic Analysismentioning
confidence: 99%
“…Kinetic and equilibrium adsorption measurements have essential role to get information for the design and operation of phosphate removal process in water/wastewater treatment (Yuchi, 2014).…”
Section: Kinetic Analysismentioning
confidence: 99%
“…The fundamental features of the conventional IXRs based on polystyrene-divinylbenzene (PS-DVB) copolymer once settled have been spotlighted by modern instrumental analyses and by in-depth studies, as summarized in a recent review. 1 One of the topics is the size of quantitatively exchangeable ions. It has been recognized that the saturated exchange capacity of tetraalkylammonium (TAA + ) ion on a cation exchange resin (CXR, -R -,M + ) decreases with an increase in size of the alkyl (R) group of TAA + (R, abbreviation, volume: methyl, TMA + , 140 Å 3 ; ethyl, TEA + , 250 Å 3 ; propyl, TPA + , 360 Å 3 ) and with an increase in cross-linking (CL) degree (CL degree, saturated % exchange for TMA + and TEA + : 2, 100, 100; 5, 90, 87; 10, 69, 63; 15, 63, 48).…”
Section: Introductionmentioning
confidence: 99%
“…However, the further elimination of non-ionic interactions between anions and the substrate can be achieved by moving anion exchange groups aside from the hydrophobic polymer surface by using long linkers [15,16]. These effects can also be explained from the view point of hydration of the functional site, as soon as more polarizable anions have higher affinity to more hydrophobic less hydrated anion exchange groups, which leads to their higher retention and sometimes considerable peak asymmetry [17,18]. In this case, moving functional groups aside from the hydrophobic polymer surface leads to their better hydration.…”
Section: Introductionmentioning
confidence: 99%