Opportunities in Nanoengineered Surface Designs for Enhanced Condensation Heat and Mass Transfer

Recent advancements in surface nanoengineering have spurred intense interests in their implementation for enhancing condensation heat transfer. When appropriately designed, nanoengineered surfaces not only lead to highly efficient transport mechanisms not achievable with conventional dropwise condensation, they also demonstrate the possibility of augmenting condensation of low surface tension fluids widely used in industry. These advantages are further enhanced by the development of highly scalable nanofabrication methods, which enable the potential transition from laboratory-scale prototypes to real-world industrial applications. In this review, we discuss the progress, opportunities, and challenges of enhancing condensation heat and mass transfer with nanoengineered surfaces. This article provides an overview of the recent developments in micro/nanoscale coating and structure fabrication techniques and performs a thorough comparison of their condensation performance, elucidating the complex interfacial transport mechanism involved. Surface structuring methods that are durable, scalable and low-cost are essential attributes for large-scale industrial implementation. Here, the methods used to improve surface durability and demonstrations of nanostructure-enhanced meter-scale condensers are presented. Limitations are discussed and the potential techniques to overcome these challenges are summarized. Given the recent development of metal additive manufacturing technology and its growing relevance in manufacturing processes, we end this review by providing our perspectives on the opportunities in enabling surface nanostructuring of metal additive manufactured materials and the potential of nanometric-millimetric co-design optimization for the development of next-generation additively manufactured condensers.

Investigation of the Kinetics and Reaction Mechanism for Photodegradation Tetracycline Antibiotics over Sulfur-Doped Bi2WO6-x/ZnIn2S4 Direct Z-Scheme Heterojunction

The rational design of direct Z-scheme heterostructural photocatalysts using solar energy is promising for energy conversion and environmental remediation, which depends on the precise regulation of redox active sites, rapid spatial separation and transport of photoexcited charge and a broad visible light response. The Bi2WO6 materials have been paid more and more attention because of their unique photochemical properties. In this study, S2− doped Bi2WO6-x coupled with twin crystal ZnIn2S4 nanosheets (Sov−BWO/T−ZIS) were prepared as an efficient photocatalyst by a simple hydrothermal method for the removal of tetracycline hydrochloride (TCH). Multiple methods (XRD, TEM, XPS, EPR, UV vis DRS, PL etc.) were employed to systematically investigate the morphology, structure, composition and photochemical properties of the as-prepared samples. The XRD spectrum indicated that the S2− ions were successfully doped into the Sov−BWO component. XPS spectra and photoelectrochemical analysis proved that S2− served as electronic bridge and promoted captured electrons of surface oxygen vacancies transfer to the valence band of T−ZIS. Through both experimental and in situ electron paramagnetic resonance (in situ EPR) characterizations, a defined direct Z-scheme heterojunction in S-BWO/T−ZIS was confirmed. The improved photocatalytic capability of S-BWO/T−ZIS results ascribed that broadened wavelength range of light absorption, rapid separation and interfacial transport of photoexcited charge, precisely regulated redox centers by optimizing the interfacial transport mode. Particularly, the Sov−50BWO/T−ZIS Z-scheme heterojunction exhibited the highest photodegradation rate was 95% under visible light irradiation. Moreover, this heterojunction exhibited a robust adsorption and degradation capacity, providing a promising photocatalyst for an organic pollutant synergistic removal strategy.

The Influence of Gas–Liquid Interfacial Transport Theory on Numerical Modelling of Plasma Activation of Water

Plasma activated water has shown great promise in a number of emerging application domains; yet the interaction between non-equilibrium plasma and liquid represents a complex multiphase process that is difficult to probe experimentally, necessitating the development of accurate numerical models. In this work, a global computational model was developed to follow the concentrations of aqueous reactive species in water treated using a surface barrier discharge in ambient air. While the two-film theory has long superseded other methods of modelling mass transfer in such areas of research as environmental and aerosol science, plasma modelling studies continue to use equilibrium and one-film theories. The transport of reactive species across the gas–liquid interface was therefore treated using the one-film and two-film theories, with the results compared to ascertain which is most appropriate for PAW modelling studies. Comparing the model-predicted concentrations to those measured, it was shown that concentrations of aqueous H+ and NO3− ions were better represented by the two-film theory, more closely fitting experimental measurements in trend and in magnitude by a factor of ten, while HNO2 and NO2− showed a slightly worse fit using this theory. This is attributed to the assumption in two-film theory of a gas-phase stagnant film which provides additional resistance to the absorption of hydrophilic species, which is absent in the one-film theory, which could be improved with a more accurate value of the Sherwood number for each species.

Advances in Dropwise Condensation: Dancing Droplets

Vapor condensation is a ubiquitous phase change phenomenon in nature, as well as widely exploited in various industrial applications such as power generation, water treatment and harvesting, heating and cooling, environmental control, and thermal management of electronics. Condensation performance is highly dependent on the interfacial transport and its enhancement promises considerable savings in energy and resources. Recent advances in micro/nano-fabrication and surface chemistry modification techniques have not only enabled exciting interfacial phenomenon and condensation enhancement but also furthered the fundamental understanding of interfacial wetting and transport. In this chapter, we present an overview of dropwise condensation heat transfer with a focus on improving droplet behaviors through surface design and modification. We briefly summarize the basics of interfacial wetting and droplet dynamics in condensation process, discuss the underlying mechanisms of droplet manipulation for condensation enhancement, and introduce some emerging works to illustrate the power of surface modification. Finally, we conclude this chapter by providing the perspectives for future surface design in the field of condensation enhancement.

Modelling the Proton-Conductive Membrane in Practical Polymer Electrolyte Membrane Fuel Cell (PEMFC) Simulation: A Review

Theoretical models used to describe the proton-conductive membrane in polymer electrolyte membrane fuel cells (PEMFCs) are reviewed, within the specific context of practical, physicochemical simulations of PEMFC device-scale performance and macroscopically observable behaviour. Reported models and their parameterisation (especially for Nafion 1100 materials) are compiled into a single source with consistent notation. Detailed attention is given to the Springer–Zawodzinski–Gottesfeld, Weber–Newman, and “binary friction model” methods of coupling proton transport with water uptake and diffusive water transport; alongside, data are compiled for the corresponding parameterisation of proton conductivity, water sorption isotherm, water diffusion coefficient, and electroosmotic drag coefficient. Subsequent sections address the formulation and parameterisation of models incorporating interfacial transport resistances, hydraulic transport of water, swelling and mechanical properties, transient and non-isothermal phenomena, and transport of dilute gases and other contaminants. Lastly, a section is dedicated to the formulation of models predicting the rate of membrane degradation and its influence on PEMFC behaviour.