Investigating chromatographic interactions in porous pigment coatings between inkjettable polyelectrolytes and model colorant solutions

被引:5
作者
Koivunen, Risto [1 ]
Jutila, Eveliina [1 ]
Bollstroem, Roger [1 ,2 ]
Gane, Patrick [1 ]
机构
[1] Aalto Univ, Sch Chem Engn, Dept Bioprod & Biosyst, POB 16300, FI-00076 Aalto, Finland
[2] Omya Int AG, Baslerstr 42, CH-4665 Oftringen, Switzerland
关键词
Polyelectrolyte; Inkjet printing; Functional printing; Functional coating; Chromatographic separation; HYDROXYAPATITE; FABRICATION; FLOW;
D O I
10.1016/j.colsurfa.2019.123676
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Printed, self-contained sensor designs based on capillary transport and microfluidic principles form a major part of current research in printed functionality. Previous work into such designs has mainly focused on cellulosic papers as base substrates. In this study, novel findings are presented employing alternative custom-designed functional pigment coated substrates, locally functionalised by inkjet printed polyelectrolytes, to separate or transport anionic or cationic molecules by surface chemistry tailoring. Both anionised and cationised coatings are tested and found to transport similarly charged model colorants successfully, while separating those of opposite charge, with the extent of separation depending on colorant concentration. Furthermore, surface chemistry reversal by cationic (polyethyleneimine, polyDADMAC) and anionic (carboxymethyl cellulose) polyelectrolyte inks is demonstrated as a complementary method for analyte separation or concentration. However, the deposition of the polyelectrolyte ink itself was found to affect the cationised coating by solubilising and re-depositing coating components, while the printed polyethyleneimine was found to be partially dissolved and transported by water elution, suggesting limited adsorption under tested conditions.
引用
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页数:13
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