Sessile Drop Method Research Articles

Study of regularities and features of simultaneous contact interaction of active and inert metal melts with zirconia

ABSTRACT The mutual influence of interface processes during simultaneous contact of zirconia ceramic plate with adhesion-active Cu–Ga–Ti melt (on one side of the plate) and inert to oxides liquid copper (on other side of the plate) was studied. Wetting of ceramic with metal melts was studied by sessile drop method, the structure of the interfaces was determined using SEM. Due to the dissolution of ceramic oxygen in Cu–Ga–Ti, non-stoichiometric zirconia (ZrO2-x) is formed, then ‘surplus’ zirconium from the ZrO2-x structure dissolves in the copper melt, the stoichiometry of zirconia is restored and an additional amount of oxygen dissolves in the Cu–Ga–Ti melt. It leads to a decrease in the adhesion of Cu–Ga–Ti to ceramics, while improving the wetting of ZrO2 ceramics with copper. The ZrO2–Cu–Ga–Ti interface contains copper–titanium–oxygen intermetallides with zirconia inclusions, which does not provide adhesion of metals with solid oxides. If the contact of Cu–Ga–Ti with ZrO2 is formed before contact with liquid copper, then the interface layer contains oxidized titanium, which promotes adhesion of metal to ceramic. Thus, the design of the sample affects the processes in the studied systems in the same way as the heating mode and the amount of the active component.

Assessing bonding and debonding properties of Evotherm modified bitumen with natural aggregates using surface free energy approach

ABSTRACT An incongruous pairing of aggregates and bitumen can result in early pavement failures such as stripping, raveling, and fatigue cracking. Surface free energy (SFE) assessments of aggregates and bitumen offer a means to evaluate the compatibility of the aggregate-bitumen system. It is important to emphasise that the SFE of both bitumen and aggregates significantly influences the determination of a compatible aggregate-bitumen combination. In this study, the moisture damage resistance of unmodified bitumen types (VG20, VG40) and modified bitumen types (PMB40, CRMB60) incorporating chemical-based warm mix asphalt (WMA) additives, specifically Evotherm, was investigated. The SFE approach was utilised to gain insights into their performance. In the laboratory, the static contact angle and SFE parameters of both unmodified and modified bitumen, with and without Evotherm, were determined using the Sessile drop method. Five different aggregate types were employed to calculate SFE performance parameters. Subsequently, the SFE performance parameter of forty combinations of aggregates and bitumen was calculated. As part of the assessment of moisture damage resistance, the compatibility ratio (CR) parameter was estimated using the dry adhesion energy, bitumen cohesion energy, wet adhesion energy, and wettability of different combinations of bitumen with aggregates. From the result, Evotherm addition to base bitumen (excluding VG20) significantly improved CR across various aggregates. Notable increases were observed for VG40, PMB40, and CRMB60 after Evotherm addition, with improvements of 66.67%, 48.48%, and 64.54% respectively for basalt aggregate. PMB40+EM with basalt aggregate exhibited the highest CR and Tensile Strength Ratio (TSR), suggesting superior moisture damage resistance compared to other bitumen combinations.

Sol-Gel Derived Alumina Particles for the Reinforcement of Copper Films on Brass Substrates.

The aim of this study is to provide tailored alumina particles suitable for reinforcing the metal matrix film. The sol-gel method was chosen to prepare particles of submicron size and to control crystal structure by calcination. In this study, copper-based metal matrix composite (MMC) films are developed on brass substrates with different electrodeposition times and alumina concentrations. Scanning electron microscopy (FE-SEM) with energy-dispersive spectroscopy (EDS), TEM, and X-ray diffraction (XRD) were used to characterize the reinforcing phase. The MMC Cu-Al2O3 films were synthesized electrochemically using the co-electrodeposition method. Microstructural and topographical analyses of pure (alumina-free) Cu films and the Cu films with incorporated Al2O3 particles were performed using FE-SEM/EDS and AFM, respectively. Hardness and adhesion resistance were investigated using the Vickers microindentation test and evaluated by applying the Chen-Gao (C-G) mathematical model. The sessile drop method was used for measuring contact angles for water. The microhardness and adhesion of the MMC Cu-Al2O3 films are improved when Al2O3 is added. The concentration of alumina particles in the electrolyte correlates with an increase in absolute film hardness in the way that 1.0 wt.% of alumina in electrolytes results in a 9.96% increase compared to the pure copper film, and the improvement is maximal in the film obtained from electrolytes containing 3.0 wt.% alumina giving the film 2.128 GPa, a 134% hardness value of that of the pure copper film. The surface roughness of the MMC film increased from 2.8 to 6.9 times compared to the Cu film without particles. The decrease in the water contact angle of Cu films with incorporated alumina particles relative to the pure Cu films was from 84.94° to 58.78°.

Enhancing antifungal and antibacterial properties of denture resins with nystatin-coated silver nanoparticles

Long-term oral health issues caused by fungi and bacteria are a primary concern for individuals who wear dentures. Denture stomatitis, primarily caused by Candida albicans (C. albicans), is a prevalent condition among denture users. Metal nanoparticles exhibit improved antimicrobial effectiveness and fewer adverse effects. This study aimed to evaluate the antifungal and antibacterial effects of nystatin-coated silver nanoparticles (Nys-coated AgNPs) embedded in acrylic resin as a more biocompatible material for denture resins. AgNPs and Nys-coated AgNPs were synthesized and characterized using UV-Vis, SEM, EDX, and DLS. Specimens of polymethyl methacrylate (PMMA) with three different concentrations of Nys, AgNPs, and Nys-coated AgNPs (0.1%, 1%, 10% w/w) were prepared. The water absorption properties of the disks and drug release were investigated for 14 days and 120 h, respectively. The hydrophilic and hydrophobic properties of the samples and their contact angles were evaluated using the sessile drop technique. The antifungal and antimicrobial activity of the prepared discs was studied against C. albicans and Streptococcus mutans, respectively. Adding Nys-coated AgNPs decreased the contact angle of discs from 67° to 49°. Furthermore, the water absorption rates of the different discs were not significantly different from those of the control groups. Results showed that Nys-coated AgNPs (10% w/w) in PMMA effectively inhibited C. albicans growth better than Nys composites (10% w/w). Additionally, Nys-coated AgNPs composites, as well as AgNPs-containing composites, showed considerable antibacterial activity against S. mutans. Nys-coated AgNPs (10% w/w) had no toxic effect on NIH3T3 cells. In conclusion, Nys-coated AgNPs could be considered a good candidate for incorporation into denture resins to address chronic oral diseases.

Effect of Cr, Al and Mo additives on the wetting characteristics of molten Ni on (Ti, Zr, Hf, Nb, Ta)C high entropy ceramics

For the first time, the wetting behavior of the (Ti, Zr, Hf, Nb, Ta)C) high entropy carbide ceramics by molten Ni-based alloys was investigated using a sessile drop technique in a vacuum environment. Adding 10wt% of Cr, Mo, or Al into Ni resulted in final contact angles of 14°, 10°, and 14° on the (Ti, Zr, Hf, Nb, Ta)C substrate, respectively. The interaction mechanism between (Ti, Zr, Hf, Nb, Ta)C and Ni-based alloys occurs in two stages: the dissolution and interaction of the elements Ti, Zr, Hf with the alloys and the dissolution of NbC and TaC at the grain boundaries. SEM observations revealed that Cr and Al additives do not interact with carbides, while Mo was dissolved in carbides. Due to the low contact angle, minimal interaction region between alloy and ceramic, and short time of drop spreading, NiAl alloy is proven to be a promising binder for the HEC-based composites.

Surface Tension of Cu-Ti Alloys and Wettability in a Liquid Alloy-Refractory Material-Gaseous Phase System.

The study involved measurements of surface tension of liquid binary copper-titanium alloys with respect to their chemical composition and temperature as well as investigations of the liquid alloy-refractory material-gaseous phase system wettability using usual refractory materials, i.e., graphite, aluminum oxide and magnesium oxide. The experiments were performed with the use of the sessile drop method and a high-temperature microscope coupled with a camera and a computer. The aim of this study was to determine the influence of titanium content in the Cu-Ti alloy on the surface tension and contact angle at the interface between the liquid alloy and the refractory material. The influence of temperature on these parameters was also examined. The tests were carried out for copper-titanium alloys with a maximum content of 1.5% wt. Ti, in the temperature range of 1373 to 1573 K. The test results indicate that as the titanium content in the alloy increases, its surface tension increases slightly. However, an increase in temperature causes a decrease in the surface tension of the alloys. In the case of an alloy containing 1.5% wt. Ti, surface tension at a temperature of 1373 K reaches 1351 mN∙m-1, and at a temperature of 1573 K, it decreases to 1315 mN∙m-1. As the temperature and titanium content in the alloy increase, a decrease in the contact angle is observed. The highest values of contact angles were recorded in the case of contact of the liquid alloy with graphite. For an alloy containing 0.1% wt. Ti at a temperature of 1373 K, the contact angle reaches 132°, while at a temperature of 1573 K, it decreases to 128°. For an alloy containing 1.5% wt. Ti, the values of contact angles are 100° and 96°, respectively. However, the contact angles have the lowest values for magnesium oxide. In the case of a temperature of 1573 K and an alloy containing 1.5% wt. Ti, the contact angle reaches 49°. Such a significant impact of titanium content on the contact angles may be due to its high affinity for oxygen (contact with a substrate made of Al2O3 and MgO and its reactivity with carbon (contact with graphite).

Wettability of a Polymethylmethacrylate Surface by Fluorocarbon Surfactant Solutions

To clarify the adsorption behavior of fluorocarbon surfactants on PMMA surfaces, the contact angles of two nonionic fluorocarbon surfactants (FNS-1 and FNS-2) and an anionic fluorocarbon surfactant (FAS) on polymethylmethacrylate (PMMA) surface were determined using the sessile drop method. Moreover, the effects of molecular structures on the surface tension, adhesion tension, solid–liquid interfacial tension, and adhesion work of the three fluorocarbon surfactants were investigated. The results demonstrate that the adsorption amounts for three fluorocarbon surfactants at the air–water interface are 4~5 times higher than those at the PMMA–solution interface. The three fluorocarbon surfactants adsorb on the PMMA surface by polar groups before CMC and by hydrophobic chains after CMC. Before CMC, FNS-2 with the smallest molecular size owns the highest adsorption amount, while FAS with large-branched chains and electrostatic repulsion has the smallest adsorption amount. After CMC, the three fluorocarbon surfactants form aggregates at the PMMA-liquid interface. FAS possesses the smallest adsorption amount after CMC. Besides, FNS-1 possesses a higher adsorption amount than FNS-2 due to the longer fluorocarbon chain and the lower CMC value of FNS-1. The adsorption behaviors of nonionic and anionic fluorocarbon surfactants on the PMMA surface are different. FAS forms interfacial aggregates before CMC, which may be attributed to the electrostatic interaction between the anionic head of FAS and the PMMA surface.

Wetting behavior of Ti-Ni-xNb filler alloy on (HfTaZrNbTi)C high-entropy carbide ceramic

Exploring the wetting behavior of active filler alloys on high-entropy ceramic is critical to clarifying the solid/liquid interface reaction mechanism and guiding the preparation of high-performance composites. The wetting and spreading behaviors of the molten Ti-Ni-xNb filler alloys, both without and with different Nb concentrations, on (HfTaZrNbTi)C high-entropy carbide (HEC) ceramic were investigated at 1330 °C under a vacuum atmosphere using a sessile drop method. The wetting process of the Ti-Ni-xNb filler alloys was characterized by four distinct stages: (i) adhesion stage, (ii) rapid decreasing stage, (iii) sluggish spreading stage, and (iv) final equilibrium stage. The Ti-Ni-xNb filler alloys all exhibited good wettability on the HEC ceramic, with the final contact angle remaining around 47-48°. The interfacial structure was identified as a sequence of HEC/Ti-based HEC’ diffusion layer/TiCx reaction layer/Ti2Ni layer/alloy droplet in all wetting systems. Notably, the introduced Nb element participated in the interfacial reactions between HEC and the filler alloy, modifying the morphology of the solidified droplet and accelerating the rapidly decreasing stage of the alloys on the ceramic. Nb atoms replaced some of the Ti atoms in the TiCx reaction layer, which restrained the atomic diffusion, leading to the formation of thinner reaction layers. The spreading kinetics were initially governed by interfacial reactions and later by the diffusion of Ti and Ni into the ceramic substrate, exhibiting a transition from reaction-controlled to diffusion-controlled spreading.

Ageing of commercial austenitic, martensitic and duplex stainless steel surfaces after formation of laser-induced periodic surface structures by fs-laser irradiation

The time-dependent wetting behavior was investigated for commercially available austenitic, martensitic and duplex stainless steel surfaces after femtosecond (fs) laser irradiation. For this purpose, highly regular LIPSS with almost identical geometric properties were generated on the stainless steels in an air environment by near-infrared fs-laser processing (λ = 1025 nm, τ = 300 fs, frep = 100 kHz, v = 0.67 m/s, Δx = 6 μm, F = 1.1 J/cm2) and compared to the polished initial surfaces as reference. The wetting with distilled water was evaluated as a function of aging time by contact angle measurements using the sessile drop method. The laser-induced morphological, topographical and chemical alteration of the surface was characterized by scanning electron microscopy, atomic force microscopy, X-ray photoelectron spectroscopy, glow-discharge optical emission spectroscopy as well as high-resolution imaging and scanning transmission electron microscopy. Despite an almost identical LIPSS-based topography alteration, the stainless steels revealed very different ageing behavior. For permanently used samples, it was shown that the ageing effect is less pronounced than for samples that were stored in ambient air following fs-laser irradiation until the wetting measurement. The results obtained make an important contribution to understanding and controlling the ageing effect of metal surfaces and thus facilitate the transfer of LIPSS-based functional surface engineering and design to industrial processes.

Reliable determination of polymeric carbon nitride wettability: A standardized sessile drop method for pressed-tablet samples

The wettability of polymeric carbon nitride (PCN) is an important surface chemical factor affecting its catalytic and separation performance. However, due to the amphipathic characteristics of hydrophilic/lipophilic and porous powder properties, the contact angle (CA) of PCN measured by the common sessile drop method will be interfered by the substrate, resulting in randomness of the results. Herein, the pristine PCNs obtained by thermal polycondensation of different precursors in air or nitrogen atmosphere were used as the wettability research object. The CA of the PCNs was measured by a modified sessile drop method after the traditional powders were replaced by pressed-tablet samples. The influence of sample mass and applied pressure on specific surface area, pore volume, surface morphology and CA of the pressed-tablet samples was investigated carefully, and the optimal experimental conditions were determined. When the sample mass was 0.15 g and the applied pressure was 10 MPa, the measured water CA of PCNs was between 27 ∼ 34°, and the diiodomethane CA is between 24 ∼ 29°. The measurement results showed considerable stability and reproducibility. This improved CA measurement method provides a simple and standardized way to accurately explore the surface chemistry of PCN, and has the potential to be applied to other hydrophilic and/or oleophilic porous powder materials.

Insights in the wettability of hard chromium coated steel for cold rolling applications

The use of toxic Cr (VI) in the chrome plating process poses significant health risks, highlighting the urgent need to find sustainable alternatives for many applications such as cold rolling. Understanding key properties of functional chrome coating in lubricated industrial processes, especially its wetting properties that can support lubrication, low friction, and durability, is essential for the development of safer coating processes. However, the wetting properties of hard chromium coating are not fully understood. This study investigates the wetting characteristics of chromium coatings in comparison to uncoated steel. The study explores the dynamic wetting behavior by conducting contact angle measurements with water and lubricant oil, determining surface free energy using the sessile drop method, and characterizing the surface through X-ray photoelectron spectroscopy analysis. The findings reveal that a standard hard chrome coating exhibits superior wettability by both water and oil and higher surface energy compared to uncoated steel. The research, supported by theoretical modelling, highlights that factors are not limited to chromium alone, but rather involve a multilayer system that includes chromium oxide and organic contaminations, which have a substantial impact on surface properties and wettability. Increased levels of organic contamination on the chrome-coated surface, are shown to result in weaker intermolecular interactions with the contacting fluid, leading to reduced surface affinity to water and consequently result in higher contact angles. Our findings provide critical insights into the intricate nature of chromium coatings and lay foundations for developing sustainable alternatives.

Optical properties of Makrofol under various alpha fluences

The optical properties of Makrofol samples are investigated under various fluences of alpha exposure (2 MeV at 5×102, 103, 5×103, 104 , 5×104, 105, 5×105 and 106 alphas.cm2 alongside the unirradiated ones (pristine). Several analyses, including UV–visible, diffused reflectance spectroscopy (DRS), photoluminescence (PL), Fourier transform infrared/attenuated total reflectance (FTIR-ATR), X-ray photoelectron spectroscopy (XPS) and sessile drop technique, are carried out to reveal the subsequent variations in the optical features of the irradiated polymer foils. The optical transmittance of the irradiated samples notably increases against the pristine ones, while it undergoes a+ plateau over various fluences. Additionally, the scattering events are more prominent in pristine samples over UV (240–400 nm) and IR (900–1040 nm) compared to the irradiated ones. While there are negligible physical alterations on the polymer surface, the photoluminescence emission gradually decreases with increasing alpha fluences in the irradiated samples mainly due to the reduction in the population of the aromatic rings. The latter is also verified by means of the surface chemical analyses such as XPS, FTIR-ATR and sessile drop/contact angle measurements. XPS reveals that the alpha particles give rise to the successive scissions of C–C and CO bonds and the consequent recombination events in the form of C–O bonds, evidenced by the changes in their abundance percentages. Concurrently, the surface hydrophilicity initially elevates up to a certain fluence and then reduces at higher fluences, indicating a couple of competitive mechanisms are involved in the context of the interactions of the alpha particles with the Makrofol polycarbonate (PC).

Adsorption of Acacia Gum on Self-Assembled Monolayer Surfaces: A Comprehensive Study Using QCM-D and MP-SPR.

The interfacial structuring of Acacia gum at various pH values on self-assembled monolayer (SAM) surfaces was investigated in order to evaluate the respective importance of surface versus biopolymer hydration in the adsorption process of the gum. To this end, SAMs with four different ending chemical functionalities (-CH3, -OH, -COOH, and -NH2) were used on gold surfaces, and the gum adsorption was monitored using multiparametric surface plasmon resonance (MP-SPR) and quartz crystal microbalance with dissipation. Surface modification with alkanethiol and the subsequent adsorption of Acacia gum were also characterized by contact angle measurements using both sessile drop and captive bubble methods. According to MP-SPR results, this study demonstrated that gum adsorbed on all surfaces and that adsorption is the most favorable at both acid pH and hydrophobic environments, i.e., when both the surface and the biopolymer are weakly hydrated and more prone to interfacial dehydration. These results reinforce our recent proposal of interfacial dehydration-induced structuring of biopolymers. Increasing the pH logically decreased the adsorption capacity, especially on a hydrophilic surface, enhancing the hydration rate of the layer. A hydrophilic surface is unfavorable to Acacia gum adsorption except if the surface presents a negative surface charge. In this case, interfacial charge dehydration was promoted by attractive electrostatic interactions between the surface and biopolymers. In the aggregate, the water percentage and the viscoelastic properties were closely related to the properties of the surface function: the negative charge and hydrophobicity significantly increased the hydration rate and viscoelastic properties with the pH, while the positive charge induced a rigid and more dehydrated layer.

Effect of Surfactants on Eliminating Stable Ultrafine Chalcopyrite Froth.

Chalcopyrite is a primary source of copper in nature. However, with the increasing need to process low-grade and complex chalcopyrite ores, overly stable froth is becoming more and more common and poses operational and safety challenges. No reliable strategy has been developed to address the issue. As a new initiative, this study investigated three different structured surfactants, sodium dodecyl sulfate (SDS), sodium dodecylbenzenesulfonate (SDBS), and pentadecafluorooctanoic acid (PFOA), which vary in hydrophobic group, aiming to modify the surfaces of ultrafine chalcopyrite particles and adjust the interfacial tension at the gas-liquid interface to eliminate stable ultrafine chalcopyrite froth. The fundamental hypothesis was that an ideal surfactant structure could adjust the particle surface wettability and interfacial tension to eliminate overly stable froth. Based on contact angle measurements and interfacial tension measurements using a Theta Flow tensiometer by the pendant drop method and the sessile drop method, it was demonstrated that the contact angle played a dominant role in defoaming, while the reduction of gas-liquid interfacial tension had an adverse effect. Additionally, defoaming tests indicated that SDBS had lower defoaming effectiveness than SDS at low surfactant concentrations due to the steric hindrance in its structure, whereas the addition of SDBS could achieve a froth reduction efficiency as high as 93.75% at higher surfactant concentrations due to its stronger hydrophobicity and adsorption capacity to chalcopyrite particles, which could reduce the contact angle from 70 to 37.62°. However, PFOA exhibited lower defoaming effectiveness than both SDS and SDBS due to its lipophobic fluorocarbon tail of PFOA and weaker adsorption capacity to chalcopyrite particles, making it unsuitable for eliminating stable ultrafine chalcopyrite froth.

Effects of UV Postcuring Times on the Color Stability, Surface Properties and Conversion of 3D-printed Temporary Resin Composites.

To evaluate the effects of UV postcuring times on color stability (CS), surface properties (wettability [°] and surface roughness [Ra]), and conversion of 3D-printed resins for temporary restorations. Disc-shaped specimens (10.0×3.0 mm) and maxillary central incisors (8.2×10.3 mm) were fabricated using provisional 3D-printed resin (PriZma Bio Prov [PZ] and PrintaX AA TEMP [PX]) in A2 shade and subjected to UV postcure times of 0 (T0), 5 (T1), 10 (T2), and 15 (T3) minutes (n=15). The incisors were used for CS evaluation with a colorimeter. In contrast, discs were used to measure the contact angle using the sessile drop method, surface roughness with an optical profilometer, and degree of conversion with FT-NIR. For CS, Ra, contact angle, and degree of conversion, a two-way ANOVA with Bonferroni post-hoc test (α=0.05) was used. PX resin demonstrated greater color stability than PZ (p=0.001). Long UV postcuring times (10 to 15 minutes) will increase the contact angle (p=0.013) and stabilize the degree of conversion (p=0.01), while 5 to 10 minutes of UV postcuring will provide better surface smoothness (p=0.04) of both resins. Long UV postcuring times (10 to 15 minutes) lead to greater alterations in color, contact angle, and stability of the degree of conversion, while 5 to 10 minutes lead to a smoother surface of the 3D-printed temporary resins.

Laser-induced protruded bioinspired texturing of Ti-6Al-4V for controlled wettability in biomedical application

Bioinspired protruded textures with variable surface morphology and characteristics are getting worldwide popularity due to their wider applications. Among them controlled wettability for different materials through bioinspired textures is very essential to reduce the adhesion, bacterial contamination and growth, and drug delivery application. Even, identification and efficient fabrication of favorable bioinspired protrusions with optimum parameters are comparatively complex from normal textures through any material processing methods due to their complex shapes, form accuracy and dimensions. Therefore, this work targets the fabrication of four different types of protruded bioinspired textures namely, fish scale, protruded square, protruded circular, Python scale (snake) textured surface on biomedical grade Ti-6Al-4V titanium alloy for controlling the wettability using femtosecond laser surface texturing (LST). The optimum process parameters for the machining of Ti-6Al-4V were set as a temporal width of 350 fs, output power of 5.5 W, wavelength of 1030 nm, scanning speed of 100 mm/s and pulse rate of 500 KHz and three repetitions for all the texture types. To examine the effect of texture type, perimeter of all the fabricated textures was kept constant. Further, effect of varying perimeters was also analyzed for perimeter ranges from 300 to 500 µm. Surface morphology and characteristics were also analyzed for the measurement of texture consistency, dimensions and composition which was also related to the wettability results examined by static contact angle of the sessile drop method. Wetting of fish scale texture is decreased with increasing perimeter whereas of all other textures, wettability is going to be improved significantly.

Relationship between Roughness and Wettability of Nine Types of Implant Surfaces and Potential Interference of Surface Oxygen and Carbon: In Vitro Evaluation.

Aim: To assess the roughness and hydrophilicity of nine types of dental implant surfaces, while also examining the presence of contaminants carbon and oxygen on these surfaces. Furthermore, the study investigated potential correlations between these characteristics across the analyzed surfaces. Materials and Methods: The surfaces analyzed were as follows: MI: machined (turned), Implacil implant; TOI: blasted with titanium oxide, Implacil implant; TOAEI: blasted with titanium oxide and acid-etched, Implacil implant; ZAED: blasted with zirconia and acid-etched, DSP implant; CPD: coated with calcium phosphate, DSP implant; XD: subjected to an experimental treatment (patent pending), DSP implant; DAEHAS: double acid-etched and activated with hydroxyapatite nano-crystals, SIN implant; DAES: double acid-etched, SIN implant; and AMP: untreated surface of the Plenum implant, produced by additive manufacturing. Four and five disc-shaped specimens were used in the hydrophilicity and roughness assessments, respectively. Roughness was evaluated by optical profilometry and scanning electron microscopy; hydrophilicity was determined using the sessile-drop technique; and the chemical analysis was performed using X-ray photoelectron spectroscopy. The Kruskal- Wallis, Mann-Whitney, and Spearman correlation tests were employed to analyze the data (p < 0.10). Results: Significant differences were observed among the analyzed surfaces in terms of both roughness and hydrophilicity (p < 0.001). The surface exhibiting the highest roughness was AMP, whereas the greatest hydrophilicity was exhibited by CPD. Correlations between roughness and hydrophobicity were observed for MI (r = 0.936, p = 0.009), ZAED (r = 0.957, p = 0.004), and DAES (r = 0.964, p = 0.005). The carbon concentration observed on the CPD surface was lower than that observed on the other surfaces, whereas the oxygen concentrations were similar. No correlations were observed between the presence of contaminants and the roughness or hydrophilicity characteristics. Conclusion: Roughness and hydrophilicity values exhibited considerable variation among the tested surfaces. Aside from the CPD surface, comparable concentrations of carbon and oxygen were detected. Although correlations between roughness and hydrophilicity were observed only for the ZAED, DAES, and MI surfaces, these correlations were inadequate to establish a causal relationship between the two surface characteristics.

The Activation of Magnesium Sintering by Zinc Addition

Light alloys based on magnesium are widely used in most areas of science and technology. However, magnesium powder alloys are quite difficult to sinter due to the stable film of oxides that counteracts diffusion. Therefore, finding a method to activate magnesium sintering is urgent. This study examines the effect of adding 5 wt. % and 10 wt. % zinc to the sintering pattern of magnesium powders at 430 °C; a dwell of 30 min was used to homogenize at the densification’s temperature. Scanning electron microscopy (SEM) was used to characterize the alloy’s microstructure, while the phase composition was characterized using X-ray diffraction (XRD) and energy dispersion spectroscopy (EDS). The sintering densities of Mg–5Zn and Mg–10Zn were found to be 88% and 92%, respectively. The results show that after sintering, a heterophase structure of the alloy is formed based on a solid solution and phases MgZn and Mg50Zn21. To establish the sintering mechanism, the interaction at the MgO and Zn melt phase interface was analyzed using the sessile drop method. The minimum contact angle—65°—was discovered at 500 °C with a 20 min holding time. It was demonstrated that the sintering process in the Mg–Zn system proceeds through the following stages: (1) penetration of zinc into oxide-free surfaces; (2) crystallization of a solid solution, intermetallics; and (3) the removal of magnesium oxide from the particle surface, with oxide particles deposited on the surface of the sample.

Droplet Microfluidic Method for Estimating the Dynamic Interfacial Tension of Ion-Crosslinked Sodium Alginate Microspheres.

The research focuses on optimizing the production of hydrogel microspheres using droplet microfluidics for pharmaceutical and bioengineering applications. A semiempirical method has been developed to predict the dynamic interfacial tension at the interface of ion-cross-linked sodium alginate microsphere-sunflower oil modified with glacial acetic acid and Tween 80 surfactant. These microspheres are produced in a small-scale coaxial device that is manufactured using affordable DLP/LCD 3D printing technology with a transparent photopolymer. The method was tested to design the minireactor in the device, which allows for the production of fully cross-linked microspheres that are ready for use at the output of the reactor without additional cross-linking steps in the microsphere collector. The mathematical expression for estimating the interfacial tension at the moment of formation of a hydrogel microsphere includes the Reynolds number for a two-phase liquid, the Ohnesorge number, and the surface tension at the liquid-air interface for continuous medium flow (modified oil). The reliability of the prediction is confirmed for continuous medium and dispersed phase flow rates of 0.8-3.2 and 0.01-0.08 mL/min, respectively. The evolution of the interfacial tension from the moment the microspheres formed and the estimated ultimate interfacial tension in a cross-linked hydrogel-modified oil system contributed to the reliable determination of the linear size of a minireactor. The ultimate interfacial tension of 76.5 ± 0.3 mN/m was determined using the Young-Laplace equation, which is based on measuring the surface free energy of the hydrogel as soft matter using the Owens-Wendt method. Additionally, the equilibrium static contact angle of the fully cross-linked hydrogel surface wetted with oil is measured using the sessile drop method. From a practical perspective, a method for optimizing and streamlining the high-tech manufacturing of cross-linked polymer microspheres and mini- and microchannel devices for use in bioengineering and pharmaceutical applications is suggested.

Study of CMAS wettability, penetration, and degradation behaviors on EB-PVD 8YSZ coatings laser micro-glazed (LMGed) by an ultraviolet picosecond ultrashort pulsed laser

CaO-MgO-Al2O3-SiO2 (CMAS) is a primary contributor to the failure of thermal barrier coatings, particularly those with columnar structures fabricated via electron beam physical vapor deposition (EB-PVD). This paper presents the laser micro glazing (LMGing) of EB-PVD using an ultraviolet pulsed ultrashort pulsed laser. With the disappearance of inter-columnar gaps, a smooth LMGed layer with extremely narrow cracks (<0.9 μm in width) were formed on the surface. Employing the sessile-drop method, heat treatment demonstrated that the LMGed layer effectively suppressed the wettability, penetration, and degradation behaviors of CMAS. Compared to the original, the spreading area of CMAS on the LMGed layer was decreased by 48 % (37.8 mm2 → 19.5 mm2), while the contact angle was increased by 116 % (6.2° → 13.4°). Meanwhile, a small amount of CMAS was found in the inter-columnar gaps, while no CMAS aggregated at the bottom. The depth of the corrosion layer at the CMAS-coating interface decreased by 68 % (9.9 μm → 3.2 μm), ensuring the blocking effect of the LMGed layer.