Underwater gas self-transportation along the femtosecond laser-written open superhydrophobic surface microchannels (< 100 µm) for bubble/gas manipulation

Underwater transportation of bubbles and gases has essential applications in manipulating and using gas, but there is still a great challenge to achieve this function at the microscopic level. Here, we report a strategy to self-transport gas along the laser-induced open superhydrophobic microchannel with a width less than 100 µm in water. The femtosecond laser can directly write superhydrophobic and underwater superaerophilic microgrooves on the polytetrafluoroethylene (PTFE) surface. In water, the single laser-induced microgroove and water medium generate a hollow microchannel. When the microchannel connects two superhydrophobic regions in water, the gas can be spontaneously transported from the small region to the large area along this hollow microchannel. The gas self-transportation can be extended to the laser-drilled microholes through a thin PTFE sheet. Anti-buoyancy unidirectional penetration is even achieved. The gas can overcome the buoyance of the bubble and spontaneously transport downward. The Laplace pressure difference drives the processes of spontaneous gas transportation and unidirectional bubble passage. We believe the property of gas self-transportation in the femtosecond laser-structured open superhydrophobic and underwater superaerophilic microgrooves/microholes has significant potential applications related to manipulating underwater gas.

Rapid Functionalization of Polytetrafluorethylene (PTFE) Surfaces with Nitrogen Functional Groups

The biocompatibility of body implants made from polytetrafluoroethylene (PTFE) is inadequate; therefore, the surface should be grafted with biocompatible molecules. Because PTFE is an inert polymer, the adhesion of the biocompatible film may not be appropriate. Therefore, the PFTE surface should be modified to enable better adhesion, preferably by functionalization with amino groups. A two-step process for functionalization of PTFE surface is described. The first step employs inductively coupled hydrogen plasma in the H-mode and the second ammonia plasma. The evolution of functional groups upon treatment with ammonia plasma in different modes is presented. The surface is saturated with nitrogen groups within a second if ammonia plasma is sustained in the H-mode at the pressure of 35 Pa and forward power of 200 W. The nitrogen-rich surface film persists for several seconds, while prolonged treatment causes etching. The etching is suppressed but not eliminated using pulsed ammonia plasma at 35 Pa and 200 W. Ammonia plasma in the E-mode at the same pressure, but forward power of 25 W, causes more gradual functionalization and etching was not observed even at prolonged treatments up to 100 s. Detailed investigation of the XPS spectra enabled revealing the surface kinetics for all three cases.

Surface potential uniformity and sensitivity of large-area PTFE electret discs of different thicknesses produced by a modified corona poling rotating system for dosimetry applications

In this study, large-area (6-cm diameter) Teflon polytetrafluoroethylene (PTFE) discs of different thicknesses (0.2-, 0.5- and 1 -mm) were negatively and positively charged by using the “modified single point-to-plane corona poling rotating system”. The effects of some crucial parameters of the PTFE disc as well as the modified corona poling rotating system on the PTFE surface potential uniformity such as: (a) PTFE disc thickness, (b) PTFE disc polarity and (c) needle-to-PTFE disc distance were successfully reported. Accordingly, closer needle-to-PTFE disc distance, positive charging mode and thinner PTFE disc provided a better PTFE surface potential uniformity. However, the effects of PTFE charge polarity and needle distance on the electrostatic charge potential uniformity were much more remarkable in comparison with the effects of PTFE thickness. Additionally, the surface potential distribution profiles of charged PTFE discs were totally flat and independent of the PTFE thickness at 5- and 13-[Formula: see text]mm needle distances for the negative and positive charging modes, respectively. At the optimized charging conditions, large-area PTFE electret disc (0.5-mm-thick) with positive uniform surface charge potential especially at the edges up to [Formula: see text] 1.8[Formula: see text]kV with stability up to 77 days studied was produced by applying a new multiple heat treatment protocol to the PTFE disc for radon dosimetry. As also observed in this study, the sensitivity of PTFE electret dosimeters to a defined radon gas concentration increases as the PTFE thickness increases. Meanwhile, 0.5-mm-thick PTFE electret disc produced was selected to be used as a high quality electret dosimeter with acceptable and superior parameters for different applications in particular medium-term radiation dosimetry in both low and high dose rate ionizing radiation fields.