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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Performance of small-domain monolithic silica columns in nano-liquid chromatography and comparison with commercial packed bed columns with 2 mu m particles
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Performance of small-domain monolithic silica columns in nano-liquid chromatography and comparison with commercial packed bed columns with 2 mu m particles

机译:纳米液相色谱中的小型域整体硅柱的性能,与2μm颗粒的商用包装床柱比较

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摘要

We report on a direct comparison of the separation performance in capillary nano-LC between commercial packed bed columns and the small-domain silica monoliths in applications. Octadecylsilylated monolithic silica capillary columns with a 50 and 100 mu m inner diameter (i.d.) were prepared with a procedure providing domain sizes in the sub-2 mu m range. The fabricated monolith columns could provide plate heights (H) of 4.0-4.2 mu m for hexylbenzene (retention factor (k) = 3.6) at an optimal linear velocity range under an isocratic condition, while showing a column permeability (K-v0 = 1.6-1.8 x 10(-14) m(2)) comparable to that of a column packed with 3-3.5 mu m particles. When the peak capacity (n(p)) for a cytochrome C digest was compared for variable gradient times (t(G) = 15, 30, 60, and 120 min) and constant gradient steepness (b'), the present monolith columns could show a 30-40% higher n(p)-value than the packed capillary column with 2 mu m particles (e.g. n(p) = 180 versus n(p) = 259 at t(G) = 30 min). The produced monolith columns showed a high chromatographic repeatability for both isocratic and gradient elution (e.g. relative standard deviation (n = 3, RSD (%)) = 0.5% for H, 2,6% for k, and 5.6% for K-v0 in the isocratic mode using the 100 mu m i.d.-columns). The present results show that the domain sizes which can now be achieved for capillary silica monoliths are sufficiently small to result in separation efficiencies that can successfully compete with the commercial packed bed columns available for use in nano-LC applications. (C) 2019 Elsevier B.V. All rights reserved.
机译:我们在商业填充床柱和应用小域石英巨石之间的毛细管纳米LC分离性能的直接比较报告。用50个100微米十八烷基硅烷块状二氧化硅毛细管柱中号内径(I.D.)用的程序提供在域尺寸制备子2微米范围内。的4.0-4.2亩所制造的单块列可以提供板的高度(H)M代表己基苯(保留因子(K)= 3.6)在等度条件下的线速度范围内具有最佳,而呈现出渗透性柱(K-V0 = 1.6 -1.8×10(-14)M(2))相媲美的填充有3-3.5微米的柱的m个粒子。当峰值容量(N(P)),用于细胞色素C消化物用于可变梯度时间(T(G)= 15,30,60,和120分钟)和恒定梯度陡度(b')中,本整料列相比可以显示30-40%的高N(p) - 值比用2亩填充毛细管柱m个粒子(例如正(p)= 180对N(p)= 259在t(G)= 30分钟)。所产生的整料列显示为两个等度和梯度洗脱高重复性色谱(例如相对标准偏差(n = 3,RSD(%))=用于h 0.5%,对于k 2,6%,和5.6%为K-V0在使用100微米等度模式M ID-列)。目前的结果显示,其现在可以为毛细管硅胶整体材料来实现域的尺寸小到足以导致分离效率可与可用于纳米LC应用中使用商业填充床栏的竞争中脱颖而出。 (c)2019 Elsevier B.v.保留所有权利。

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