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使用全水流动相制备和研究用于最小化反相色谱柱保留损失的双组分二氧化硅改性疏水层。

Preparation and investigation of two-component silica-modified hydrophobic layer for minimizing retention loss of reversed-phase chromatographic columns using fully aqueous mobile phases.

作者信息

Gritti Fabrice, Lawrence Nicole, Field Jessica

机构信息

Waters Corporation, Instrument/Core Research/Fundamental, 34 Maple Street, Milford, MA, 01757, USA.

Waters Corporation, Instrument/Core Research/Fundamental, 34 Maple Street, Milford, MA, 01757, USA.

出版信息

J Chromatogr A. 2024 Mar 29;1719:464766. doi: 10.1016/j.chroma.2024.464766. Epub 2024 Feb 27.

Abstract

Chromatographers often employ fully aqueous mobile phases to retain highly polar compounds in reversed-phase liquid chromatography (RPLC). However, when the flow rate is interrupted, either accidentally or intentionally, a substantial loss in retention occurs due to the spontaneous dewetting of water from the hydrophobic surface of conventional RPLC-C particles. Previous studies have shown that maintaining a low C surface coverage (approximately 1.5 μmol/m) can mitigate water dewetting by increasing chain disorder, facilitating the intercalation of water clusters between the C-bonded chains, and keeping the mesopores wetted. In this research, we explore the potential and additional benefits of using two-component surface bonding materials (C/C and PhenylHexyl (PhHx)/C) at a constant and low total surface coverage of 1.51 ± 0.15 μmol/m. We synthesized seven one- and two-component modified silica particles with a volume average particle size of 5.22 μm and an average mesopore size of 104 Å. The surface coverage was increased from 0 to 0.54, 1.00, and to 1.66 μmol for C chains and from 0 to 0.52, 0.70, and to 1.65 μmol for PhHx ligands. To prevent interactions between water and any unreacted silanols, all seven derivatized particles were heavily endcapped with trimethylsilane (TMS) reagent. The fraction of the surface area remaining in contact with water was determined by measuring the retention times of weakly (thiourea) and strongly (thymine) retained compounds at intervals of 1, 2, 4, 8, 16, 32, and 64 minutes following the cessation of flow. Two distinct column temperatures, 24°C and 60°C, were employed in the experiments. Retention losses were found to be minimized in the presence of a small quantity of C chains (less than 40% of the total surface coverage). Additionally, it is essential to consider substantial fractions of PhHx chains, as long as the presence of the PhHx ligand does not significantly impact retention and selectivity. Combining mixed RPLC bondings with a low total surface coverage of approximately 1.5 μmol/m emerges as a viable solution for further minimizing retention loss in standard C18-bonded RPLC columns, particularly within the surface coverage range of 2.5-3.0 μmol/m.

摘要

在反相液相色谱(RPLC)中,色谱工作者常常采用全水流动相来保留高极性化合物。然而,当流速意外或有意中断时,由于常规RPLC-C颗粒疏水表面上的水自发脱湿,保留率会大幅下降。先前的研究表明,保持较低的C表面覆盖率(约1.5 μmol/m²)可以通过增加链的无序度、促进水簇在C键合链之间的嵌入以及保持中孔湿润来减轻水的脱湿。在本研究中,我们探讨了在总表面覆盖率恒定且较低(1.51±0.15 μmol/m²)的情况下使用双组分表面键合材料(C/C和苯基己基(PhHx)/C)的潜力和额外益处。我们合成了七种单组分和双组分改性硅胶颗粒,其体积平均粒径为5.22 μm,平均中孔尺寸为104 Å。C链的表面覆盖率从0增加到0.54、1.00和1.66 μmol/m²,PhHx配体的表面覆盖率从0增加到0.52、0.70和1.65 μmol/m²。为了防止水与任何未反应的硅醇之间发生相互作用,所有七种衍生颗粒都用三甲基硅烷(TMS)试剂进行了大量封端。通过测量流动停止后1、2、4、8、16、32和64分钟时弱保留(硫脲)和强保留(胸腺嘧啶)化合物的保留时间,确定与水接触的剩余表面积分数。实验采用了24°C和60°C两个不同的柱温。发现在存在少量C链(小于总表面覆盖率的40%)的情况下,保留损失最小化。此外,只要PhHx配体的存在不会显著影响保留率和选择性,就必须考虑大量的PhHx链。将总表面覆盖率约为1.5 μmol/m²的混合RPLC键合相结合,是进一步最小化标准C18键合RPLC柱中保留损失的可行解决方案,特别是在2.5 - 3.0 μmol/m²的表面覆盖率范围内。

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