Issue 16, 2010

Growth of solid conical structures during multistage drying of sessile poly(ethylene oxide) droplets

Abstract

Sessile droplets of aqueous poly(ethylene oxide) solution, with average molecular weight of 100 kDa, are monitored during evaporative drying at ambient conditions over a range of initial concentrations c0. For all droplets with c0 ≥ 3%, central conical structures, which can be hollow and nearly 50% taller than the initial droplet, are formed during a growth stage. Although the formation of superficially similar structures has been explained for glass-forming polymers using a skin-buckling model which predicts the droplet to have constant surface area during the growth stage (L. Pauchard and C. Allain, Europhys. Lett., 2003, 62, 897–903), we demonstrate that this model is not applicable here as the surface area is shown to increase during growth for all c0. We interpret our experimental data using a proposed drying and deposition process comprising the four stages: pinned drying; receding contact line; “bootstrap” growth, during which the liquid droplet is lifted upon freshly-precipitated solid; and late drying. Additional predictions of our model, including a criterion for predicting whether a conical structure will form, compare favourably with observations. We discuss how the specific chemical and physical properties of PEO, in particular its amphiphilic nature, its tendency to form crystalline spherulites rather than an amorphous glass at high concentrations and its anomalous surface tension values for MW = 100 kDa may be critical to the observed drying process.

Graphical abstract: Growth of solid conical structures during multistage drying of sessile poly(ethylene oxide) droplets

Supplementary files

Article information

Article type
Paper
Submitted
30 Oct 2009
Accepted
12 Feb 2010
First published
03 Mar 2010

Phys. Chem. Chem. Phys., 2010,12, 3998-4004

Growth of solid conical structures during multistage drying of sessile poly(ethylene oxide) droplets

D. Willmer, K. A. Baldwin, C. Kwartnik and D. J. Fairhurst, Phys. Chem. Chem. Phys., 2010, 12, 3998 DOI: 10.1039/B922727J

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