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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Addition of methanol to the mobile phase in packed capillary column supercritical fluid chromatography Retention mechanisms from linear solvation energy relationships
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Addition of methanol to the mobile phase in packed capillary column supercritical fluid chromatography Retention mechanisms from linear solvation energy relationships

机译:填充毛细管柱超临界流体色谱法中向流动相中添加甲醇的线性溶剂化能量关系的保留机理

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Linear solvation energy relationships (LSERs) were used to verify previously proposed retention mechanisms when an organic modifier is used with an octyldecylsilane bonded phase in packed capillary column supercritical fluid chromatography. Supercritical fluid chromatographic retention data for a wide variety of compounds at different modifier concentrations were obtained using a 60 cmX200 mu.m I.D. ODS packed capillary column. Supercritical carbon dioxide at a pressure of 260 atm was used as mobilephase and methanol as modifier. The LSER regression equation used was log k'=SP_o+llog ~(16)+s pi_2~H+a alpha_2~H+b beta_2~H+ rR_2, where k' represents the capacity factor and L~(16) represents the partition coefficient of the solute between the gas phase and n-hexadecane at 298 K, and l, s, a, b and r are the regression coefficients. By increasing the percentage of modifier added to the mobile phase, the / coefficient decreased gradually. The b and s coefficients were greatly decreased on moving from neat carbon dioxide mobile phase to 2% methanol modifier, thereafter showing a gradual decrease with increasing modifier concentration. From these observations, we substantiate the conclusion that when a small amount of modifier (up to 2%) is added, the predominent modifier effect on the ODS bonded phase is dynamic coating of free silanols on the surface of the stationary phase, and when more modifier is added, another effect, i.e. an increase in the density of the mobile phase leading to an increase inelution strength of the eluent, becomes more important.
机译:当在填充毛细管柱超临界流体色谱中将有机改性剂与辛基癸基硅烷键合相一起使用时,线性溶剂化能量关系(LSERs)用于验证先前提出的保留机理。使用60 cmX200μmI.D.获得了各种化合物在不同改性剂浓度下的超临界流体色谱保留数据。 ODS填充毛细管柱。压力为260 atm的超临界二氧化碳用作流动相,甲醇用作改性剂。使用的LSER回归方程为log k'= SP_o + llog〜(16)+ s pi_2〜H + a alpha_2〜H + b beta_2〜H + rR_2,其中k'代表容量因子,L〜(16)代表分区气相和正十六烷之间在298 K时的溶质系数为l,s,a,b和r为回归系数。通过增加添加到流动相中的改性剂的百分比,/系数逐渐降低。当从纯净的二氧化碳流动相转移到2%的甲醇改性剂时,b和s系数大大降低,此后随着改性剂浓度的增加而逐渐降低。从这些观察结果中,我们证实了以下结论:当添加少量的改性剂(最高2%)时,对ODS键合相的主要改性剂作用是在固定相表面动态涂覆游离硅烷醇,而当更多时,添加改性剂后,另一种作用(即增加流动相的密度导致洗脱液的洗脱强度增加)变得更加重要。

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