Search Results (68)

Two-phase expansion processes have emerged as a promising technology for enhancing energy efficiency in power generation, refrigeration, waste heat recovery systems (for example, partially evaporated organic Rankine cycle, organic flash cycle, and trilateral flash cycle), oil and gas, and other applications. However, despite their potential, widespread adoption is hindered by inherent challenges, particularly energy losses that reduce operational efficiency. This review systematically evaluates the current state of two-phase expansion technologies, focusing on the root causes, impacts, and mitigation strategies for expansion losses. This work used Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA). Using the PRISMA framework, 52 relevant publications were identified from Scopus and Web of Science to conduct the systematic review. A preliminary co-occurrence analysis of keywords was also conducted using VOSviewer version 1.6.20. Three clusters were observed in this co-occurrence analysis. However, the results may not be significant. Therefore, the extended work was done through a comprehensive analysis of experimental and simulation studies from the literature. This study identifies critical loss mechanisms in key components of two-phase expanders, such as the nozzle, diffuser, rotor, working chamber, and vaneless space. Also, losses arising from wetness, such as droplet formation, interfacial friction, and non-equilibrium phase transitions, are examined. These phenomena degrade performance by disrupting flow stability, increasing entropy generation, and causing mechanical erosion. Several losses in the turbine and volumetric expanders operating in two-phase conditions are reported. Ejectors, throttling valves, and flashing flow systems that exhibit similar challenges of losses are also discussed. This review discusses the mitigation and the strategy to minimize the two-phase expansion losses. The geometry of the inlet of the two-phase expanders plays an important role, which also needs improvement to minimize losses. The review highlights recent advancements in addressing these challenges and shows optimization opportunities for further research. Full article

Microplastics (MPs), particularly fibrous MPs, have emerged as a significant environmental concern due to their pervasive presence in aquatic and terrestrial ecosystems. The textile industry is a significant contributor to MP pollution, particularly through the production of synthetic fibers and natural/synthetic blends, which release substantial amounts of fibrous MPs. Among the various types of MPs, fibrous MPs account for approximately 49–70% of the total MP load found in wastewater globally, primarily originating from textile manufacturing processes and the domestic laundering of synthetic fabrics. MP shedding poses a significant challenge for environmental management, requiring a comprehensive examination of the mechanisms and strategies for the mitigation involved. To address the existing knowledge gaps regarding MP shedding during the textile production processes, this brief review examines the current state of MP shedding during textile production, covering both dry and wet processes, and identifies the sources and pathways of MPs from industrial wastewater treatment plants to the environment. It further provides a critical evaluation of the existing recycling and upcycling technologies applicable to MPs, highlighting their current limitations and exploring their potential for future applications. Additionally, it explores the potential for integrating sustainable practices and developing regulatory frameworks to facilitate the transition towards a circular economy within the textile industry. Given the expanding application of textiles across various sectors, including medical, agricultural, and environmental fields, the scope of microplastic pollution extends beyond conventional uses, necessitating urgent attention to the impact of fibrous MP release from both synthetic and bio-based textiles. This brief review consolidates the current knowledge and outlines the critical research gaps to support stakeholders, policymakers, and researchers in formulating effective, science-based strategies for reducing textile-derived microplastic pollution and advancing environmental sustainability. Full article

Frequent agricultural irrigation events continuously raise the groundwater table on loess platforms, triggering numerous loess landslides and significantly contributing to soil erosion in the Chinese Loess Plateau. The movement of irrigation water within the surficial loess layer is crucial for comprehending the mechanisms of moisture penetration into thick layers. To investigate the infiltration and evaporation processes of irrigation water, a large undisturbed soil column with a 60 cm inner diameter and 100 cm height was extracted from the surficial loess layer. An irrigation simulation event was executed on the undisturbed soil column and the ponding infiltration and subsequent evaporation processes were systematically monitored. A ruler placed above the soil column recorded the ponding height during irrigation. Moisture probes and tensiometers were installed at five depths to monitor the temporal variations in volumetric water content (VWC) and matric suction. Additionally, an evaporation gauge and an automatic weighing balance measured the potential and actual evaporation. The results revealed that the initially high infiltration rate rapidly decreased to a stable value slightly below the saturated hydraulic conductivity (K_s). A fitted Mezencev model successfully replicated the ponding infiltration process with a high correlation coefficient of 0.995. The monitored VWC of the surficial 15 cm-thick loess approached a saturated state upon the advancing of the wetting front, while the matric suction sharply decreased from an initial high value of 65 kPa to nearly 0 kPa. The monitored evaporation process of the soil column was divided into an initial constant rate stage and a subsequent decreasing rate stage. During the constant rate stage, the actual evaporation closely matched or slightly exceeded the potential evaporation rate. In the decreasing rate stage, the actual evaporation rate fell below the potential evaporation rate. The critical VWC ranged from 26% to 28%, with the corresponding matric suction recovering to approximately 25 kPa as the evaporation process transitioned between stages. The complete evaporation process was effectively modeled using a fitted Rose model with a high correlation coefficient (R² = 0.971). These findings provide valuable insights into predicting water infiltration and evaporation capacities in loess layers, thereby enhancing the understanding of water movement within thick loess deposits and the processes driving soil erosion. Full article

The low adhesion of water drops on superhydrophobic surfaces is a prerequisite for their widespread potential industrial applications. The wetting transition between different wetting states significantly influences the dynamic behavior of water drops on solid surfaces. Although some theoretical studies have addressed wetting transitions, the underlying mechanisms by which local micro- and nanostructure parameters on superhydrophobic surfaces affect the wetting transition have not been fully elucidated. This study investigates three-dimensional micropillared and micro/nanopillared superhydrophobic surfaces, deriving thermodynamically the equation for the free energy barrier of wetting transition, which is influenced by the overall roughness of the entire superhydrophobic surface and its local micro/nanostructures. Theoretical calculations are performed to investigate the effects of various micro- and nanostructure parameters on the free energy barrier and wetting transition. Based on the principle of energy minimization and the calculated free energy barrier, the possible wetting states on superhydrophobic surfaces are analyzed and compared with experimental results. This study contributes to the theoretical understanding of wetting transitions and may guide the design of superhydrophobic surfaces for diverse applications. Full article

Superhydrophobicity is closely linked to the chemical composition and geometric characteristics of surface roughness. Building on our structural studies on water and air–water interfaces, this work aims to elucidate the mechanism underlying the wetting transition from the Wenzel to the Cassie state on a hydrophobic surface. In the Wenzel state, the grooves are filled with water, meaning that the surface roughness becomes embedded in the liquid. To evaluate the effects of surface roughness on water structure, a wetting parameter (W_Roughness) is proposed, which is closely related to the geometric characteristics of roughness, such as pillar size, width, and height. During the wetting transition from Wenzel to Cassie states, the critical wetting parameter (W_Roughness,c) may be expected, which corresponds to the critical pillar size (a_c), width (w_c), and height (h_c). The Cassie state is expected when the W_Roughness is less than W_Roughness,c (<W_Roughness,c), which can be achieved by altering the geometric characteristics of the roughness, such as increasing pillar size (>a_c), decreasing width (<w_c), or increasing height (>h_c). Additionally, molecular dynamic (MD) simulations are conducted to demonstrate the effects of surface roughness on superhydrophobicity. Full article

Surface wettability, the interaction between a liquid droplet and the surface it contacts, plays a key role in influencing droplet behavior and flow dynamics. There is a growing interest in designing surfaces with tailored wetting properties across diverse applications. Advanced fabrication techniques that create surfaces with unique wettability offer significant innovation potential. This study investigates the wettability transition of laser-textured anisotropic surfaces featuring shark skin-inspired microstructures using four post-processing methods: spray coating, isopropyl alcohol (IPA) treatment, silicone oil treatment, and silanization. The impact of each method on surface wettability was assessed through water contact angle measurements, scanning electron microscopy (SEM), and laser scanning microscopy. The results show a transition from superhydrophilic behavior on untreated laser-textured surfaces to various (super)hydrophobic states following surface treatment. Chemical treatments produced different levels of hydrophobicity and anisotropy, with silanization achieving the highest hydrophobicity and long-term stability, persisting for one year post-treatment. This enhancement is attributed to the low surface energy and chemical properties of silane compounds, which reduce surface tension and increase water repellence. In conclusion, this study demonstrates that post-processing techniques can effectively tailor surface wettability, enabling a wide range of wetting properties with significant implications for practical applications. Full article

This study investigated the influence of the ultraviolet (UV) dose (${\mathrm{D}}^{\mathrm{U}\mathrm{V}}$) on the photodeposition of MnO_x and Pd cocatalysts on 300-nm-thick anatase TiO₂ thin films, which were prepared via sol–gel dip-coating on a glass substrate. MnO_x and Pd were photodeposited using increasing UV doses ranging from 5 to 20 J cm⁻², from 5 mM aqueous electrolytes based on Mn²⁺/IO₃⁻ or Pd²⁺, respectively. The effect of the ${\mathrm{D}}^{\mathrm{U}\mathrm{V}}$ on the MnO_x photodeposition resulted in an increase in Mn²⁺ surface content, from 2.7 to 5.2 at.%, as determined using X-ray photoelectron spectroscopy (XPS). For Pd, increasing the UV dose led to a reduction in the oxidation state, transitioning from Pd²⁺ to Pd⁰, while the overall Pd surface content range remained relatively steady at 2.2–2.4 at.%. Both MnO_x/TiO₂ and Pd/TiO₂ exhibited proportional enhancements in photocatalytic activity towards the degradation of methylene blue. Notably, Pd/TiO₂ demonstrated a significant improvement in photocatalytic performance, surpassing that of pristine TiO₂. In contrast, TiO₂ samples functionalized through wet impregnation and thermal treatment in the same electrolytes showed overall lower photocatalytic activity compared to those functionalized via photodeposition. Full article

Due to their mechanical robustness and chemical resistance, composite electrospun membranes based on polyvinyl chloride (PVC) are suitable for sensor applications. Aiming to improve the electrical characteristics of these membranes, this work investigated the effects of the addition of carbon nanotubes (CNTs) to PVC electrospun membranes, in terms of morphology and thermal and impedance behavior. Transmission electron microscopy images evidenced that most of the nanotubes were encapsulated within the fibers and oriented along them, while field-emission scanning electron micrographs revealed that the membranes consisted of uniform fibers with an average diameter of 339 ± 31 nm, regardless of the addition of the carbon nanotubes. With respect to the neat resin, the addition of nanotubes caused a significant lowering of the glass transition temperature (up to 20 °C) and a marked change in the second degradation step of PVC. Nyquist plots from electrical impedance spectra showed a charge transfer resistance (R_CT) of 38 and 40 MΩ for neat PVC and PVC/CNT 3 wt.% membranes, respectively, indicating that, in the dry state, the encapsulation of CNTs in the fibers and the high porosity of the membranes prevented the formation of a percolation network, increasing the electrical resistance. In the wet state, however, there was a greater change in the impedance behavior, decreasing the resistance R_CT to 4.5 and 1.1 MΩ, for neat PVC and PVC/CNT 3 wt.% membranes, respectively. The results of this study, showing a significant variation in impedance behavior between dry and wet membranes, are relevant for the development of various types of sensors based on PVC composites. Full article

Binary As_xSe_100−x alloys from the border of a glass-forming region (65 < x < 70) subjected to nanomilling in dry and dry–wet modes are characterized by the XRPD, micro-Raman scattering (micro-RS) and revised positron annihilation lifetime (PAL) methods complemented by a disproportionality analysis using the quantum–chemical cluster modeling approach. These alloys are examined with respect to tetra-arsenic biselenide As₄Se₂ stoichiometry, realized in glassy g-As₆₅Se₃₅, glassy–crystalline g/c-As₆₇Se₃₃ and glassy–crystalline g/c-As₇₀Se₃₀. From the XRPD results, the number of rhombohedral As and cubic arsenolite As₂O₃ phases in As-Se alloys increases after nanomilling, especially in the wet mode realized in a PVP water solution. Nanomilling-driven amorphization and reamorphization transformations in these alloys are identified by an analysis of diffuse peak halos in their XRPD patterning, showing the interplay between the levels of a medium-range structure (disruption of the intermediate-range ordering at the cost of an extended-range one). From the micro-RS spectroscopy results, these alloys are stabilized by molecular thioarsenides As₄Se_n (n = 3, 4), regardless of their phase composition, remnants of thioarsenide molecules destructed under nanomilling being reincorporated into a glass network undergoing a polyamorphic transition. From the PAL spectroscopy results, volumetric changes in the wet-milled alloys with respect to the dry-milled ones are identified as resulting from a direct conversion of the bound positron–electron (Ps, positronium) states in the positron traps. Ps-hosting holes in the PVP medium appear instead of positron traps, with ~0.36–0.38 ns lifetimes ascribed to multivacancies in the As-Se matrix. The superposition of PAL spectrum peaks and tails for pelletized PVP, unmilled, dry-milled, and dry–wet-milled As-Se samples shows a spectacular smoothly decaying trend. The microstructure scenarios of the spontaneous (under quenching) and activated (under nanomilling) decomposition of principal network clusters in As₄Se₂-bearing arsenoselenides are recognized. Over-constrained As_6·(2/3) ring-like network clusters acting as pre-cursors of the rhombohedral As phase are the main products of this decomposition. Two spontaneous processes for creating thioarsenides with crystalline counterparts explain the location of the glass-forming border in an As-Se system near the As₄Se₂ composition, while an activated decomposition process for creating layered As₂Se₃ structures is responsible for the nanomilling-driven molecular-to-network transition. Full article

Since Chernozems are among the most fertile soils in the world, the study of their degradation is of great interest. However, the microstructure and composition of the soil organic matter (SOM) in eroded Chernozems have not yet been sufficiently studied. We studied the SOM and aggregate states of eroded Chernozems using the example of two catenas with arable Haplic Chernozems in the Kursk region of Russia. In the plow horizons (the part of the soil most susceptible to water erosion), we determined the mean-weighted aggregate diameter (MWD), structure and water stability coefficients (SC and WS; dry and wet sieving, respectively), soil organic carbon (SOC) content, and SOM composition and content (qualitative and quantitative micromorphological analyses, respectively). It was shown that with an increase in the degree of erosion, the content of SOC decreased significantly, according to both chemical and micromorphological methods of evaluation. No significant relationships were found between the degree of erosion and the indicators of the structure (except for WS, which was significantly lower in non-eroded Chernozem than in slightly and moderately eroded soils). With the increasing degree of erosion, the humus state of these soils deteriorates at the microlevel, the intensity of humification decreases, the depth of the appearance of assimilated biogenic aggregates with finely dispersed calcite in the profile increases, the structure is destroyed, lumpy aggregates form, and the proportion of planar voids increases. The downslope transport of the soil solid phase under the impact of erosion is accompanied by the accumulation of the transformation products of carbohydrates in the Chernozems in the lower part of the catena. In the Chernozems located in the transit position of the slope, the composition of SOM is characterized by the predominance of lipids and nitrogen-containing compounds. Our unique results contribute to a deeper understanding of the formation of structure and water resistance in eroded soils. Full article

An approach to derive the below-bandgap absorption in GaSb/GaAs self-assembled quantum dot devices using room-temperature external quantum efficiency measurement results is presented. Devices with five layers of delta-doped quantum dots placed in the intrinsic, n- and p-regions of a GaAs solar cell are studied. The importance of incorporating an extended Urbach tail absorption in analyzing the absorption strength of quantum dots and the transition states is demonstrated. The theoretically integrated absorbance via quantum dot ground states is calculated as 1.04 × 10¹⁵ cm⁻¹s⁻¹, which is in reasonable agreement with the experimentally derived value 8.1 × 10¹⁵ cm⁻¹s⁻¹. The wetting layer and quantum dot absorption contributions are separated from the tail absorption and their transition energies are calculated. Using these transition energies and the GaAs energy gap of 1.42 eV, the heavy hole confinement energies for the quantum dots (320 meV) and for the wetting layer (120 meV) are estimated. Full article

Introduction: Wetting affects chemical and physical properties. In aluminum, superhydrophobic surfaces keep fog, ice, and corrosion at bay. Biomimicry replicates natural processes. The high surface energy of aluminum limits its intrinsic dewetting properties. Existing surface modification methods have disadvantages, such as hazardous chemicals, high costs, and harsh processing conditions. This work is environmentally friendly and overcomes traditional limitations. Methods: Aluminum alloy plates (AA5083) of commercial grade (ASTM-B-209M) were used in the study. Stationary friction stir processing (sFSP) was carried out on a universal milling machine focused solely on surface characteristics using transition metal powders (99% purity). The prepared samples were polished with abrasive papers to 1000 grit after processing. In the microwave hot water treatment (mHWT), processed and unprocessed samples were processed for 10 min at 800 W. A silanization agent was vapor-deposited on the samples following mHWT at 55 °C for 60 min. Results: The low-strain-rate sFSP of aluminum alloys results in substantial grain refinement, reaching ~1 µm for processed samples and ~30 µm for unprocessed samples. Refined grains have a dense and networked nanostructure after mHWT. After silanization, the samples exhibit excellent contact angles (>155°), low tilt angles (10°), and low contact angle hysteresis (5°). The processed samples, featuring highly refined grains, demonstrate low water adhesion (~16 µN) compared to unprocessed samples (~50 μN), attributed to the high interfacial energy of the Cassie state, effectively entrapping air. These processed samples exhibit remarkable de-wetting properties and mechanical resilience, owing to the strong negative capillary pressure (>1100 kPa) generated by highly dense networked nanostructures. Conclusions: In conclusion, the research helps to develop sustainable and durable superhydrophobic aluminum surfaces. The environmentally friendly and cost-effective strategies explored have far-reaching implications for industrial applications, emphasizing opportunities for advancements and practical utilization across various industries. Full article

In the quest to mitigate carbon dioxide emissions, it becomes essential to address the existing atmospheric CO₂. Effective and economical methodologies, particularly those without additional energy consumption, are crucial. Currently, a leading method is the direct capture of CO₂ using ion exchange resins, which achieve the adsorption and desorption of carbon dioxide simply by using the humidity variations. This technology, though minimizing additional energy cost, still needs improvement in its efficiency in CO₂ capture capacity and compared to other methods. In this work, we develop low-cost techniques to reduce the AmberLite™ IRA900 Cl (IRA-900) anion exchange resin to micro size, and observe significant performance enhancement on CO₂ capture efficiency contingent on reducing the particle diameters. This performance disparity is attributed to the differential water adsorption capacities inherent in particles of diverse diameters. Our results reveal that smaller resin particles outperform their larger counterparts, exhibiting accelerated adsorption rates and expedited transitions from wet to dry states. Notably, these smaller particles display a quintupled enhancement in adsorption efficacy relative to non-treated particles and a marked increase in relative adsorption capacity. Upon treatment, IRA-900 demonstrates robust CO₂ processing efficiency, achieving a peak adsorption rate of 1.28 g/mol·h and a maximum desorption rate of 1.18 g/mol·h. Also, the material is subjected to almost 100 cycles of testing, and even after 100 cycles, the resin particles maintain a capacity of 100%. Moreover, our material can be fully regenerated to 100% efficiency by simply immersing it in water. Simultaneously, storing it in water allows for the long-term maintenance of its performance without other treatment methods. A key observation is the resin’s sustained performance stability post extended exposure to humid conditions. These outcomes offer substantial practical implications, emphasizing the relevance of our study in practical environmental applications. Full article

Nanocellulose fiber materials were considered promising biomaterials due to their excellent biodegradability, biocompatibility, high hydrophilicity, and cost-effectiveness. However, their low proton conductivity significantly limited their application as proton exchange membranes. The methods previously reported to increase their proton conductivity often introduced non-biodegradable groups and compounds, which resulted in the loss of the basic advantages of this natural polymer in terms of biodegradability. In this work, a green and sustainable strategy was developed to prepare cellulose-based proton exchange membranes that could simultaneously meet sustainability and high-performance criteria. Adenine and thymine were introduced onto the surface of tempo-oxidized nanocellulose fibers (TOCNF) to provide many transition sites for proton conduction. Once modified, the proton conductivity of the TOCNF membrane increased by 31.2 times compared to the original membrane, with a specific surface area that had risen from 6.1 m²/g to 86.5 m²/g. The wet strength also increased. This study paved a new path for the preparation of environmentally friendly membrane materials that could replace the commonly used non-degradable ones, highlighting the potential of nanocellulose fiber membrane materials in sustainable applications such as fuel cells, supercapacitors, and solid-state batteries. Full article

During the concrete mixing process, the transition of aggregates from a dry to a moist state introduces a crucial dynamic that significantly influences particle interaction, consequently impacting mixing homogeneity. In this paper, based on the discrete element method, the effect of aggregate moisture on the mixing process of sand and stone was investigated. The interaction between dry particles was described by the Hertz–Mindlin model, while the interaction between wet particles was calculated by the linear cohesion model considering the liquid bridge force. Additionally, a functional relationship between the moisture content and the parameters of the linear cohesive contact model was established. The results show that the numerical method can be employed to simulate the mixing process. Notably, when the moisture content of pebbles ranges from 0% to 0.75% and that of sand ranges from 0% to 10.9%, the linear cohesion model is deemed suitable. The standard deviation of the mixing homogeneity of wet particles is lower than that of dry particles for short mixing time, indicating that a small amount of liquid enhances mixing homogeneity. However, moisture has no obvious effect on mixing homogeneity for a long mixing time. This nuanced understanding of the interplay between moisture, particle interactions, and mixing duration contributes valuable insights to optimize concrete mixing processes. Full article