2006
DOI: 10.1134/s0036024406080267
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Influence of flow parameters of the mobile phase on the retention and thermodynamic characteristics of sorption in gas-liquid chromatography

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Cited by 9 publications
(4 citation statements)
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“…Standard thermodynamic functions (enthalpy and entropy ) of sorption of organic com pounds under conditions of a distributive mechanism of sorption are characterized by a change in these functions upon transition of 1 mol of gaseous sorbate under ideal gas conditions at P st = 1 atm and column temperature to an infinitely dilute solution in the sta tionary liquid phase [6]. The calculated values of and for mesophase N* and isotropic phase I of the binary sorbent are presented in Table 4.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Standard thermodynamic functions (enthalpy and entropy ) of sorption of organic com pounds under conditions of a distributive mechanism of sorption are characterized by a change in these functions upon transition of 1 mol of gaseous sorbate under ideal gas conditions at P st = 1 atm and column temperature to an infinitely dilute solution in the sta tionary liquid phase [6]. The calculated values of and for mesophase N* and isotropic phase I of the binary sorbent are presented in Table 4.…”
Section: Resultsmentioning
confidence: 99%
“…Dimensionless con stants of sorption ( = 1 atm, = ) [6], activity coefficients (a symmetric reference system) characterizing deviation from Raoult's law when small samples of sorbate are dis solved in a stationary liquid phase, and the standard and excess thermodynamic characteristics of sorption along with factors of isomer separation,…”
Section: Sorption and Selective Properties Of Binary Liquid Crystallimentioning
confidence: 99%
“…). Взаимосвязь K H с V g T в условиях линейной равновесной модели ГЖХ дана в работе [23]: Для оценки влияния добавки Ас-Ts-β-CD в ЖК на стандартные термодинамические функции сорбции рассчитывали разности этих величин, полученных на колонках с бинарной (LC-CD) и исходной (LC) неподвижными фазами:…”
Section: экспериментunclassified
“…The temperature dependence of the specific retention volume V g allows one to calculate the enthalpy of sorption Δ H S : Some researchers proposed to consider the changes of inner energy U 1 S instead of enthalpy of sorption Δ H S . Since Δ H S = U 1 S + RT , at typical temperature of chromatographic experiment about 400 K, the correction RT is about 3 kJ/mol, i.e., small in comparison with the reported Δ H S values.…”
Section: Introductionmentioning
confidence: 99%