RESUMEN
Recently, intensive research has been conducted on the development of bacterial repelling surfaces because of the disadvantages of the conventional bactericidal leaching and contact-killing surfaces for practical application. Among these bacteria-repelling methodologies, zwitterionic polymers were widely investigated because of its excellent nonfouling properties, but its durability has limited its widespread use since most of the surfaces were developed by constructing polymer brushes via atom transfer radical polymerization (ATRP). In this study, we developed zwitterionic polymer surfaces with desirable mechanical and chemical durability for long-term use through simple blending of poly(sulfobetaine methacrylate) (PSBMA)/poly(ether sulfone) (PES) semi-interpenetrated networked microgels with hydrophobic PES polymer matrix. Results show that the as-prepared surfaces can efficiently induce hydration layers and, thus, reduce the bacterial attachment through resisting nonspecific protein adsorption. The bacterial adhesion for Escherichia coli and Staphylococcus aureus was investigated under both flow and static conditions. This work has set a paradigm for developing durable antibacterial surfaces with nonfouling properties.
RESUMEN
Growing demands for bio-friendly antifouling surfaces have stimulated the development of new and ever-improving material paradigms. Despite notable progress in bio-friendly coatings, the biofouling problem remains a critical challenge. In addition to biofouling characteristics, mechanically stressed surfaces such as ship hulls, piping systems, and heat exchangers require long-term durability in marine environments. Here, we introduce a new generation of anti-biofouling coatings with superior characteristics and high mechanical, chemical and environmental durability. In these surfaces, we have implemented the new physics of stress localization to minimize the adhesion of bio-species on the coatings. This polymeric material contains dispersed organogels in a high shear modulus matrix. Interfacial cavitation induced at the interface of bio-species and organogel particles leads to stress localization and detachment of bio-species from these surfaces with minimal shear stress. In a comprehensive study, the performance of these surfaces is assessed for both soft and hard biofouling including Ulva, bacteria, diatoms, barnacles and mussels, and is compared with that of state-of-the-art surfaces. These surfaces show Ulva accumulation of less than 1%, minimal bacterial biofilm growth, diatom attachment of 2%, barnacle adhesion of 0.02 MPa and mussel adhesion of 7.5 N. These surfaces promise a new physics-based route to address the biofouling problem and avoid adverse effects of biofouling on the environment and relevant technologies.
Asunto(s)
Incrustaciones Biológicas , Estrés Mecánico , Animales , Adhesión Bacteriana , Bivalvos/fisiología , Diatomeas/fisiología , Flavobacteriaceae/fisiología , Propiedades de Superficie , Ulva/fisiologíaRESUMEN
Gas hydrate formation is a high-risk and common flow assurance problem in subsea oil production plants. The modern strategies to mitigate hydrate formation have switched from thermodynamic inhibition to risk management. In this new mitigation strategy, hydrate formation is allowed as long as it does not lead to plugging of pipelines. Thus, understanding the growth kinetics of gas hydrates plays a critical role in risk management strategies. Here, we report a new accurate and in situ approach to probe the kinetics of gas hydrate formation. This approach is based on the hot-wire method, which probes the thermal properties of the medium surrounding the hot-wire. As the thermal properties of gas hydrate and its initial constituents are different, variation in these properties is used to probe kinetics of hydrate growth front. Through this in situ method, we determine kinetics of cyclopentane hydrate formation in both mixing and flow conditions. The findings show that at ambient pressure and a temperature of 1-2 °C, the hydrate formation rate under mixing condition varies between 1.9 × 10-5 and 3.9 × 10-5 kg m-2 s-1, while in flow condition, this growth rate drops to 4.5 × 10-6 kg m-2 s-1. To our knowledge, this is the first reported growth rate of cyclopentane hydrate. This in situ approach allows us to probe kinetics of hydrate formation where there is no optical access and provides a tool to rationally design risk management strategies for subsea infrastructures.
RESUMEN
Advancement in high-performance photonics/electronics devices has boosted generated thermal energy, making thermal management a bottleneck for accelerated innovation in these disciplines. Although various methods have been used to tackle the thermal management problem, evaporation with nanometer fluid thickness is one of the most promising approaches for future technological demands. Here, we studied thin-film evaporation in nanochannels under absolute negative pressure in both transient and steady-state conditions. We demonstrated that thin-film evaporation in nanochannels can be a bubble-free process even at temperatures higher than boiling temperature, providing high reliability in thermal management systems. To achieve this bubble-free characteristic, the dimension of nanochannels should be smaller than the critical nucleolus dimension. In transient evaporative conditions, there is a plateau in the velocity of liquid in the nanochannels, which limits the evaporative heat flux. This limit is imposed by liquid viscous dissipation in the moving evaporative meniscus. In contrast, in steady-state condition, unprecedented average interfacial heat flux of 11 ± 2 kW cm-2 is achieved in the nanochannels, which corresponds to liquid velocity of 0.204 m s-1. This ultrahigh heat flux is demonstrated for a long period of time. The vapor outward transport from the interface is both advective and diffusion controlled. The momentum transport of liquid to the interface is the limiting physics of evaporation at steady state. The developed concept and platform provide a rational route to design thermal management technologies for high-performance electronic systems.
RESUMEN
Evaporation is a fundamental and core phenomenon in a broad range of disciplines including power generation and refrigeration systems, desalination, electronic/photonic cooling, aviation systems, and even biosciences. Despite its importance, the current theories on evaporation suffer from fitting coefficients with reported values varying in a few orders of magnitude. Lack of a sound model impedes simulation and prediction of characteristics of many systems in these disciplines. Here, we studied evaporation at a planar liquid-vapor interface through a custom-designed, controlled, and automated experimental setup. This experimental setup provides the ability to accurately probe thermodynamic properties in vapor, liquid, and close to the liquid-vapor interface. Through analysis of these thermodynamic properties in a wide range of evaporation mass fluxes, we cast a predictive model of evaporation based on nonequilibrium thermodynamics with no fitting parameters. In this model, only the interfacial temperatures of liquid and vapor phases along with the vapor pressure are needed to predict evaporation mass flux. The model was validated by the reported study of an independent research group. The developed model provides a foundation for all liquid-vapor phase change studies including energy, water, and biological systems.