Solid surface mapping by inverse gas chromatography

被引:3
作者
Gutiérrez, MC
Osuna, S
Baráibar, I
机构
[1] Inst Nacl Tecn Aeroespacial, Cooperac Bilateral, Subdirecc Gen Relac Inst & Polit Comercial, Madrid 28850, Spain
[2] Ctr Astrobiol, INTA, CSIC, Madrid 28850, Spain
关键词
surface free energy; inverse gas chromatography; surface mapping;
D O I
10.1016/j.chroma.2005.03.047
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Inverse gas chromatography (IGC) at infinite dilution, is a technique for characterising solid surfaces. Current practice is the injection of n-alkane homologous series to obtain the free energy of adsorption of the CH2 group, from which the London component of the solid surface free energy, y(S)(d), is calculated. A value around 40 mJ/m(2) is obtained for poly(ethylene), and 30 mJ/m2 for a clean glass fibre, while the potential surface interactivity of a glass fibre is far greater than that of poly(ethylene). A specific component of the surface, in mJ/m2, should be calculated in order to obtain significant parameters. As applied up to date, when calculating the specific component of the surface energy, the fact that W-a(sp) energy values are in a totally different scale than AN or DN values is a major drawback. Consequently, Ka and Kb values obtained are in arbitrary energy units, different from those of the London component measured by injecting the n-alkane series. This paper proposes a method to obtain Ka and Kb values of the surface in the same energetic scale than the London component. The method enables us to correct the traditional London component of a solid, obtaining a new value, where the amount of W-aCH2 accounting for Debye interactions with polar sites, is excluded. As a result, an approach to surface mapping is performed in several different substrate materials. We show results obtained on different solid surfaces: poly(ethylene), clean glass fibre, glass beads, chemically modified glass beads and carbon fibre. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:142 / 149
页数:8
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