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A facile one-step method of roughened copper foils of 0.0076 ​mm thickness heated on the open flame for 15 ​s produced superhydrophilic surfaces that exhibited superwetting at average radial growths of 10.8 ​mm/s following drop dispensation. Superhydrophilicity was found to deteriorate over time and XRD analysis ruled out compositional change as the cause of this behaviour. Instead, SEM imaging revealed wrinkled 20–30 ​nm-thick nanoflakes that were predominantly stretched out initially to engender superwetting properties via Wenzel wetting. These extended microstructures folded up with time due to relaxation of the residual stresses from the thermal oxidation process, resulting in temporal reduction in superhydrophilicity, which can be restored by reapplying thermal oxidation. The impingement of air with 80 psi pressure on the substrate also caused similar deterioration. The superwetting characteristic also endowed these substrates with anti-bacterial properties where a 56% reduction in bacteria count with Staphylococcus epidermidis was found.

Polymerase Chain Reaction (PCR) amplifies specific deoxyribonucleic acid (DNA) targets whereby the reaction vessels are placed in high thermal inertia media and subjected to multiple cycles of discrete temperatures to effect denaturation, annealing and extension events. Precise temperature control and efficient heat transfer are crucial factors in achieving amplification reproducibility and reliability as well as in reducing the time required for PCR. Understanding the temperature distribution and transfer characteristics during PCR will facilitate system optimization to enhance the efficiency of DNA amplification. We describe a numerical thermal study investigating temperature profiles achieved using the classical method of manual transfer of PCR reaction vessels through a series of temperature-controlled media compared with that of a more recently reported method that displaces reaction vessels spatially by tilting through different temperature zones. It was found that while the classical method allows the reagent to achieve uniform temperature distribution, natural convection effects would necessitate translation speeds in excess of 150 mm/min in order to limit the reagent temperature drop to within 10 °C. With the tilt method, uniform temperature distributions as well as temperature settling times within 5 s could be attained. The simulation results demonstrated here indicate that the tilt method can be developed further to augment extreme PCR requiring less than 2s for each cycle.

The use of superhydrophilic surfaces for superwetting applications can be hampered by their wetting degradation over time. In this work, superhydrophilic surfaces were fabricated by graphene oxide (GO) deposition on roughened polyvinyl chloride (PVC) substrates. These surfaces were found to exhibit zero contact angle when enhanced green fluorescent protein (EGFP) was deposited on the surface immediately after GO was applied. However, when the GO-coated substrate was stored for 3 h, the surface displayed a contact angle of 54°. The main contact line spreading of the EGFP drop was more easily discernible using normal (500 lx, low glare and shadow free) lighting than with blue LED lighting in the dark. The average radius of the spreading main contact line was found to follow a power-law relationship that increased at a faster rate with higher relative humidity. Confocal imaging revealed rings of EGFP deposition following superwetting that is attributable to pinning around the islands of GO accumulation. Substrate superhydrophilic and superwetting properties can be preserved by adequate control of relative humidity. Relative humidity of 80 % was easily maintained for 150 min by incorporating a 20 μL water drop in a sealed 240-mL container.

A system devised to conduct Polymerase Chain Reaction (PCR) in-flight on drones that uses the spatial displacement of capillary tubes on thermal blocks kept at 94 °C, 58 °C and 72 °C corresponding to cycling temperatures for denaturation, annealing and extension is demonstrated here. The use of acetal as the thermal block material reduced heat loss and the input power (within 18.5 W) needed to maintain the required temperatures. Tests showed that concentrations of samples down to 1.16 × 106 DNA copies/μL could be significantly and consistently detected above the background emission of the fluorescence signal intensity.

A drop-based approach to facilitate the remediation of methylene blue (MB) solution via catalytic degradation with silver nanowires on a superhydrophobic substrate with a 2 mm hole without fouling is presented here. Studies on the dynamical response of drop removal via pressure rate perturbation, showed greater elapsed times at the 7.61 μL/s air flowrate with 25 μL and 30 μL volume drops than at higher air flowrates used. These results are accounted for by the rate of air flow through the plastron, used to equilibrate the lowering of pressure in the transparent receptacle that tends to prevent drop dislodgement, being only able to operate up to a specific upper limit. A method that calculates the absorbance values based on the intensity spectrum of the nanowire solution as reference was found to reveal the time progress degradation of MB solution by spectrometry. It showed that a 25 μL drop of the MB solution could be degraded within 15 s using 0.25 mg of the silver nanowire.