We developed an open microfluidic system to dispense and manipulate discrete droplets on planar plastic sheets. Here, a superhydrophobic material is spray-coated on commercially-available plastic sheets followed by the printing of hydrophilic symbols using an inkjet printer. The patterned plastic sheets are taped to a two-axis tilting platform, powered by stepper motors, that provides mechanical agitation for droplet transport. We demonstrate the following droplet operations: transport of droplets of different sizes, parallel transport of multiple droplets, merging and mixing of multiple droplets, dispensing of smaller droplets from a large droplet or a fluid reservoir, and one-directional transport of droplets. As a proof-of-concept, a colorimetric assay is implemented to measure the glucose concentration in sheep serum. Compared to silicon-based digital microfluidic devices, we believe that the presented system is appealing for various biological experiments because of the ease of altering design layouts of hydrophilic symbols, relatively faster turnaround time in printing plastic sheets, larger area to accommodate more tests, and lower operational costs by using off-the-shelf products.
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Highly efficient fog harvesting on superhydrophobic microfibers through droplet oscillation and sweeping
Water droplet transport on fibers is of great importance for achieving high water collection efficiency from fog. Here, we exploit a new droplet sliding mechanism to accelerate the droplet coalescence and collection for highly efficient fog harvesting by coating hydrophilic microfibers with superhydrophobic layers of assembled carbon nanoparticles. We find that during the initial water collection, unlike the pinned droplets having axisymmetric barrel shapes wrapped around uncoated microfibers, the hanging droplets on coated microfibers with non-wrapping clamshell shapes are highly mobile due to their lower contact hysteresis adhesion; these are observed to oscillate, coalesce, and sweep the growing droplets along the horizontally placed microfibers. The driving force for droplet transport is mainly ascribed to the coalescence energy release and fog flow. After introducing small gravity force by tilting coated microfibers with a small angle of 5°, we find that it can effectively drive the oscillating mobile droplets for directional transport by rapidly sweeping the droplets with a much higher frequency. Finally, the water collection rate from fog on uncoated microfibers over a prolonged duration is found to be improved over 2 times after superhydrophobic coating, and it is further enhanced over 5 times after a small tilting angle of 5°.
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- Award ID(s):
- 1745921
- NSF-PAR ID:
- 10101152
- Date Published:
- Journal Name:
- Soft Matter
- Volume:
- 14
- Issue:
- 41
- ISSN:
- 1744-683X
- Page Range / eLocation ID:
- 8276 to 8283
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract Coalescence‐induced droplet jumping phenomena on superhydrophobic surfaces can significantly enhance their heat transfer performances by effectively removing droplets from the surfaces. However, understanding the ideal design for condensing surfaces is still challenging due to the complex nature of droplet dynamics associated with their nucleation, coalescing, and jumping mechanisms. The intrinsic dynamic nature of droplet behaviors suggests the use of hierarchical concave morphology to account for the different length scales associated with each transport phenomenon. The hierarchical morphology thereby enables heterogeneous wetting characteristics by realizing both microscale droplets on superhydrophobic surfaces and nanoscale pinning regions beneath the droplets by arresting liquid residues after droplet jumping. Heat transfer performances are further examined by extracting physically meaningful descriptors, such as nucleation sites, droplet growth rates, and droplet jumping frequency, showing 44% enhancements when droplet nucleation sites are designed in selective locations.
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null (Ed.)The fog-basking behavior of the Onymacris unguicularis, a beetle species living in the coastal regions of the Namibian desert, has recently caught the attention of the engineering community, as suggesting a viable biomimetic approach to address the problem of harvesting water in arid regions of the globe. Previous research has focused on observation and analysis of the beetle’s elytron properties and how these affect fog-collection rates. The head stance taken by the Onymacris unguicularis when fog basking is well documented. However, how this stance affects droplet collection has not been studied up to now. The present paper addresses this problem from a computational fluid dynamics perspective, where three-dimensional numerical simulations are used to characterize the fog flow properties around a simplified geometry mimicking the beetle’s body. The simulations employ two-way coupling between the gas flow and the dispersed fog phase to account for feedback effects of fog droplets on the carrier fluid (air), and assume that droplets are captured after hitting the elytron surface. The study considers several combinations of free-stream velocity and droplet volume fraction. The analysis reveals that there is a range of head-stance angles, corresponding to an inclination of the beetle between 35 deg and 45 deg with respect to the horizon, that maximizes water collection on the beetle’s back, in qualitative agreement with observations in nature and laboratory experiments. A rationale is proposed to explain this phenomenon, finding that the specific head stance corresponds to the maximum residence time of fluid particles above the beetle’s elytron surface. This, in turn, designates the maximum likelihood for water droplets to be captured in the boundary layer developing over the beetle and subsequently hit the surface where they get captured. The results reveal the importance of the fluid flow pattern around the beetle’s body in addition to the microphysical properties of the elytron when reliable predictions of the water droplet collection efficiency are sought.more » « less
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Abstract. Extractive electrospray ionization (EESI) has been a well-knowntechnique for high-throughput online molecular characterization of chemicalreaction products and intermediates, detection of native biomolecules, invivo metabolomics, and environmental monitoring with negligible thermal andionization-induced fragmentation for over two decades. However, the EESIextraction mechanism remains uncertain. Prior studies disagree on whetherparticles between 20 and 400 nm diameter are fully extracted or if theextraction is limited to the surface layer. Here, we examined the analyteextraction mechanism by assessing the influence of particle size and coatingthickness on the detection of the molecules therein. We find that particlesare extracted fully: organics-coated NH4NO3 particles with afixed core volume (156 and 226 nm in diameter without coating) showedconstant EESI signals for NH4NO3 independent of the shell coatingthickness, while the signals of the secondary organic molecules comprisingthe shell varied proportionally to the shell volume. We also found that theEESI sensitivity exhibited a strong size dependence, with an increase insensitivity by 1–3 orders of magnitude as particle size decreasedfrom 300 to 30 nm. This dependence varied with the electrospray (ES)droplet size, the particle size and the residence time for coagulation in theEESI inlet, suggesting that the EESI sensitivity was influenced by thecoagulation coefficient between particles and ES droplets. Overall, ourresults indicate that, in the EESI, particles are fully extracted by the ESdroplets regardless of the chemical composition, when they are collected bythe ES droplets. However, their coalescence is not complete and dependsstrongly on their size. This size dependence is especially relevant whenEESI is used to probe size-varying particles as is the case in aerosolformation and growth studies with size ranges below 100 nm.more » « less
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- Free Publicly Accessible Full Text
-
Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1039/C8SM01688G
