2005
DOI: 10.1016/j.chroma.2005.04.070
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Effect of temperature on the chromatographic retention of ionizable compounds

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Cited by 33 publications
(24 citation statements)
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“…As discussed above, at higher pH (pH 4.2 or 5.2), because ion-exchange interaction was greater, the pK a of the bases becomes an important parameter governing retention. As proposed in previous literature [8,9,24], the pK a of solutes decreases with increasing temperature, and the smaller the pKa of the base is, the more it decreases. Since the pK a value of epirubicin (pK a 8.08) is smaller than that of daunorubicin (pK a 8.46), a greater reduction of the protonated species will be obtained for epirubicin.…”
Section: Temperature Effect At Various Buffer Phsmentioning
confidence: 53%
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“…As discussed above, at higher pH (pH 4.2 or 5.2), because ion-exchange interaction was greater, the pK a of the bases becomes an important parameter governing retention. As proposed in previous literature [8,9,24], the pK a of solutes decreases with increasing temperature, and the smaller the pKa of the base is, the more it decreases. Since the pK a value of epirubicin (pK a 8.08) is smaller than that of daunorubicin (pK a 8.46), a greater reduction of the protonated species will be obtained for epirubicin.…”
Section: Temperature Effect At Various Buffer Phsmentioning
confidence: 53%
“…As discussed above, ion-exchange interaction is responsible for retention of solutes at higher pHs. However, it is a slow mass transfer step [9], thus leading to lower efficiency. With increasing temperature, improved efficiencies are observed at all the pHs tested.…”
Section: Temperature Effect At Various Buffer Phsmentioning
confidence: 99%
See 1 more Smart Citation
“…This is especially true for polar and ionizable compounds since ionization equilibria are temperature dependent. A systematic study of the effect of temperature (25-508C) on the retention of ionizable compounds in methanol-water mobile phases [104] and ACN-water mobile phases [105] showed significant changes in selectivity. This has been demonstrated repeatedly in the literature, yet its potential role in method development is often underestimated.…”
Section: Selectivitymentioning
confidence: 99%
“…The same is true for the buffer. The s s pK a for phosphate at pH 2.8 and 7.9 and acetate at pH 5.5 in 25% MeCN did not change at all in the range from 15 to 508C, while the values for piperazine, Tris, and butylamine decreased by about 1 pH unit [191]. For butylamine, the s s pK a value changed by about 1 unit from 20 to 508C in a methanol-based mobile phase [190].…”
Section: Methods Developmentmentioning
confidence: 93%