The effects of molecular weight, evaporation rate and polymer concentration on pillar formation in drying poly(ethylene oxide) droplets

被引:21
作者
Baldwin, K. A. [1 ,2 ]
Fairhurst, D. j. [1 ]
机构
[1] Nottingham Trent Univ, Sch Sci & Technol, Nottingham NG11 8NS, England
[2] Univ Nottingham, Sch Phys & Astron, Nottingham NG7 2RD, England
关键词
Droplet; Evaporation; Polymer; Deposit; Poly(ethylene oxide); Ring-stain; FLOW; SUPPRESSION; DIFFUSION;
D O I
10.1016/j.colsurfa.2012.10.049
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
Typically, when droplets of dilute suspensions are left to evaporate the final dry deposit is the familiar coffee-ring stain, with nearly all the solute deposited at the initial contact line. Contrastingly, in previous work we have shown that sessile droplets of poly(ethylene oxide) (PEO) solutions form tall central pillars (or monoliths) during a 4-stage drying process. We show that a dimensionless Peclet-type number Pe, a ratio of the competing advective and diffusive motion of the dissolved polymer, which incorporates the effects of evaporation rate, initial concentration co and the polymer diffusion coefficient, to determine whether the droplet will form a pillar or a flat deposit. In this work we vary concentration up to c(0) =0.5 and molecular weight M-w between 3.35 kg/mol and 600 kg/mol and find that in ambient conditions with c(0) = 0.1 pillars only form for a limited range, 35 <= M-w <= 200 kg/mol. This observation is in contrast to the the Peclet argument in which high molecular weight polymers with a slow self-diffusion should still form pillars. We present various experimental measurements attempting to resolve this discrepancy: crossover time-scale for viscoelastic behaviour; fast diffusion of an entangled network; and droplet viscosity or contact line friction. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:867 / 871
页数:5
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