Hydrophobic Surface Research Articles

Zeolite Crystallization Inside Chemically Recyclable Ordered Nanoporous Co3O4 Scaffold: Precise Replication and Accelerated Crystallization.

The synthesis of mesoporous zeolites has garnered attention with regard to improving their catalytic and adsorption performances. While the hard-templating method provides opportunities to design precisely controlled hierarchical micro- and mesoporous structures, synthesizing mesoporous zeolites without external precipitation requires significant work. This is mainly due to the absence of usable templates other than carbon with hydrophobic surfaces. Herein, it is demonstrated that the Co3O4 template is valuable in preparing mesoporous silicalite-1 and ZSM-5 with a precisely controlled porous structure through hydrothermal synthesis. Unlike conventional carbon templates, the Co3O4 template is relatively hydrophilic, effective in suppressing external precipitation, and is reusable by dissolving in an acidic solution. The crystallization process also differs from that of the carbon template, as the silicate precipitates on a 3D ordered nanoporous Co3O4 scaffold, followed by crystallization and crystal growth. Furthermore, it is unexpectedly observed that the zeolite crystallization is accelerated in the Co3O4 template. The synthetic approach utilizing nanoporous metal oxides opens new doors for the control of the hierarchical structure of zeolites, as well as for the design of metal oxide-zeolite nanocomposite catalysts, due to the potential extensibility of the combination of metal oxides and zeolites.

Improving the Efficiency of Submersible Multistage Pumps Based on the Hydrophobization of the Flow Part Surfaces

The paper presents an experimental study of an assembly of five stages of an electric centrifugal pump (ECP) installation, the flow part of which is modified according to the principles of biomimetics, namely using the “lotus leaf effect”. The object of the study was a 5A-35 ECP. The surfaces of the blade systems of impellers and guide devices of stages 5 A-35 were hydrophobized using the method of applying surfactant layers. The degree of impellers hydrophobicity was estimated by the wetting angle average value measured by three drops at three different points on the impeller surface. The impellers surface roughness under study was determined by the arithmetic mean profile deviation Ra and the profile height irregularities Rz. The issues related to the surfactant coating modification effect salt deposition and corrosion were studied. For this purpose, the surfaces of the original and modified impellers were subjected to intensive forced salt deposition as a result of prolonged exposure to saline solution. The conclusion about the samples corrosion resistance degree was made by changing their mass, which was due to the salt deposits formation during 15 hours of stay in solution, as well as using the drop method. Both methods have shown that the surfactant coating can serve as a salt deposition inhibitor, and the pump impeller modified by it has increased corrosion resistance. Thus, during comparative tests, a smaller mass of salt was deposited on the modified impeller sample during 15 hours of exposure in saturated saline solution than on the original sample. This indicates that the surfactant layer prevents the salt deposits fixation on the working surfaces of the pump stage. On the modified sample examined by the drop method, the indicator color changed in 20 minutes, and on the original one – in 2 minutes. Experimental studies have been carried out, during which the operation energy parameters of a five stages 5A-35 pumping package with initial and modified surfactant-coated impellers have been determined. The studies have shown a 2 % increase in efficiency in the pum-ping package of stages with modified impellers. The results of the study can be useful in the oil production, chemical industry, as well as in the housing and communal services sector.

Highly Alternating Copolymer of [1.1.1]Propellane and Perfluoro Vinyl Ether: Forming a Hydrophobic and Oleophobic Surface with

Utilizing the unique properties of fluorine substitution is an effective strategy for constructing highly functional materials. Here, we synthesized a novel copolymer composed of [1.1.1]propellane and perfluoro(propyl vinyl ether) (PPVE), rich in alternating sequences. The spin-coated copolymer film was amorphous, and its surface exhibited an extremely low surface free energy (γ). The γ value was lower than that of polytetrafluoroethylene despite containing only 40 mol % PPVE units. This can be attributed to the cancellation of the C-F dipole moments by the entirely random orientation of the fluorine units.

Disrupting Mycobacterium smegmatis biofilm using enzyme-immobilized rifampicin loaded silk fibroin nanoparticles for dual anti-bacterial and anti-biofilm action

Biofilm formation is a major challenge in the treatment of tuberculosis, leading to poor treatment outcomes and latent infections. The complex and dense extracellular polymeric substances (EPS) of the biofilm provides safe harbour for bacterium enabling persistence against anti-TB antibiotics. In this study, we demonstrated that rifampicin-encapsulated silk fibroin nanoparticles immobilized with antibiofilm enzymes can disrupt the Mycobacterium smegmatis biofilm and facilitate the anti-bacterial action of Rifampicin (RIF). The EPS of M.smegmatis biofilm predominantly comprised of lipids (48.8 ± 1.32 %) and carbohydrates (34.8 ± 4.70 %), similar to tuberculosis biofilms. Pre-formed biofilm eradication screening revealed that hydrolytic enzymes such as β-Glucosidase, Glucose oxidase, ɑ-Amylase, Acylase, and Phytase can exhibit biofilm eradication of M.smegmatis biofilms. The enzyme-mediated biofilm disruption was associated with a decrease in hydrophobicity of biofilm surfaces. Treatment with β-glucosidase and Phytase demonstrated a putative biofilm eradication by reducing the total carbohydrates and lipid composition without causing any significant bactericidal activity. Further, Phytase (250 μg/ml) and β-Glucosidase (112.5 ± 17.6 μg/ml) conjugated rifampicin-loaded silk fibroin nanoparticles (R-SFNs) exhibited an enhanced anti-bacterial activity against pre-formed M.smegmatis biofilms, compared to free rifampicin (32.5±7 μg/ml). Notably, treatment with β-glucosidase, Phytase and ɑ-amylase immobilized SFNs decreased the biofilm thickness by ∼98.84 % at 6h, compared to control. Thus, the study highlights that coupling anti-mycobacterial drugs with biofilm-eradicating enzymes such as amylase, phytase or β-glucosidase can be a potential strategy to improve the TB therapeutic outcomes.

Robust Metal Oxide Adhesion Layers for Cellulose Nanofiber-Based QCM Sensors.

Here, we demonstrate the significant role of robust metal oxide adhesion layers on the cellulose nanofiber (CNF)-based quartz crystal microbalance (QCM) humidity sensor characteristics including sensitivity and stability. In this study, we deposited various metal oxide films (NiO, TiO2, ZnO, and WO3) onto QCM Au electrodes as adhesion layers before drop-casting CNF dispersion water. These metal oxide adhesion layers significantly enhanced the stability of CNF films on QCM sensors even in a high-humidity environment where a conventional adhesion layer (polyethylenimine) for CNF could not maintain stable adhesion. There was a significant difference between different metal oxide layers in the QCM data for humidity sensing. We found a negative correlation between the QCM sensitivity and the water wettability of metal oxide surfaces. Morphology analysis of the deposited CNF films revealed that the center-concentrated CNF microstructures on the metal oxide adhesion layers rigorously explained the observed negative correlation between the sensitivity and the wettability of metal oxide surfaces. This trend was further confirmed by gradually changing the hydrophobicity of the NiO adhesion surfaces. Thus, the proposed strategy using robust metal oxide adhesion layers will be a foundation for further development of various CNF-based QCM gas sensors.

Enhanced surface acoustic wave microfluidic performance through FDTS self-assembled monolayers on [formula omitted]

Microfluidics technology has been extensively applied in biochemical analysis and medical diagnostics, where precise and efficient control of microfluids is crucial. However, existing passive microfluidic control methods (e.g., microchannels) and active strategies (e.g., optical, thermal, magnetic field, and electrokinetic manipulation) are often hindered by complex device structures and operational uncertainties. Surface acoustic wave (SAW) microfluidic manipulation offers a promising alternative, providing flexible and efficient digital microfluidic control through the modulation of input signals. Nevertheless, the intrinsic hydrophilicity of substrates such as LiNbO3 results in inefficient microfluidic driving and jetting, primarily due to high surface tension. In this study, we employed chemical vapor deposition (CVD) to coat LiNbO3 substrates with 1H,1H,2H,2H-Perfluorododecyltrichlorosilane (FDTS) self-assembled monolayers (SAMs), creating hydrophobic surfaces with a contact angle of approximately 120°. In comparison to commercially available Glaco hydrophobic coatings, which reduce SAW amplitude by approximately threefold and increase substrate temperature by up to 1.5 times, FDTS SAMs exhibit negligible impact on SAW properties. Furthermore, when compared to untreated SAW devices, FDTS SAMs-coated devices demonstrated a sixfold increase in droplet driving speed under low power input (e.g., 0.5 W), enabling faster and more precise liquid jetting at velocities reaching 5 m/s. This work highlights the potential of FDTS SAMs in enhancing the performance of SAW-driven microfluidic devices, particularly in applications requiring high-efficiency droplet manipulation.

Active-bromide and surfactant synergy for enhanced microfouling control.

Biofilms are structured microbial communities encased in a matrix of self-produced extracellular polymeric substance (EPS) and pose significant challenges in various industrial cooling systems. A nuclear power plant uses a biocide active-bromide for control of biological growth in its condenser cooling system. This study is aimed at evaluating the anti-bacterial and anti-biofilm efficacy of active-bromide against planktonic and biofilm-forming bacteria that are commonly encountered in seawater cooling systems. The results demonstrated that active-bromide at the concentration used at the power plant (1 ppm) exhibited minimal killing activity against Pseudomonas aeruginosa planktonic cells. The bacterial cell surface hydrophobicity assay using Staphylococcus aureus and P. aeruginosa indicated that Triton-X 100 significantly decreased the hydrophobicity of planktonic cells, enhancing the susceptibility of the cells to active-bromide. Biofilm inhibition assays revealed limited efficacy of active-bromide at 1 ppm concentration, but significant inhibition at 5 ppm and 10 ppm. However, the addition of a surfactant, Triton-X 100, in combination with 1 ppm active-bromide displayed a synergistic effect, leading to significant biofilm dispersal of pre-formed P. aeruginosa biofilms. This observation was substantiated by epifluorescence microscopy using a live/dead bacterial assay that showed the combination treatment resulted in extensive cell death within the biofilm, as indicated by a marked increase in red fluorescence, compared to treatments with either agent alone. These findings suggest that active bromide alone may be insufficient for microfouling control in the seawater-based condenser cooling system of the power plant. Including a biocompatible surfactant that disrupts established biofilms (microfouling) can significantly improve the efficacy of active bromide treatment.

Fucoidan-Vegetable Oil Emulsion Applied to Myosin of Silver Carp: Effect on Protein Conformation and Heat-Induced Gel Properties.

How to improve the gel properties of protein has become a research focus in the field of seafood processing. In this paper, a fucoidan (FU)-vegetable oil emulsion was prepared, and the mechanism behind the effect of emulsion on protein conformation and the heat-induced gel properties was studied. The results revealed that the FU-vegetable oil complex caused the aggregation and cross-linking of myosin, as well as increased the surface hydrophobicity and total sulfhydryl content of myosin. In addition, the addition of the compound (0.3% FU and 1% vegetable oil) significantly improved the gel strength, hardness, chewiness, and water-holding capacity of the myosin gel (p < 0.05). In particular, when the addition of camellia oil was 1%, the gel strength, hardness, chewiness, and water-holding capacity had the highest values of 612.47 g.mm, 406.80 g, 252.75 g, and 53.56%, respectively. Simultaneously, the emulsion (0.3% FU-1% vegetable oil) enhanced the hydrogen bonds and hydrophobic interaction of the myosin gels. The image of the microstructure showed that the emulsion with 0.3% FU-1% vegetable oil improved the formation of the stable three-dimensional network structure. In summary, the FU-vegetable oil complex can promote unfolding of the protein structure and improve the gel properties of myosin, thus providing a theoretical basis for the development of functional surimi products.

Surface hydrophobicity mechanism of poultry red mite, Dermanyssus gallinae (Acari: Dermanyssidae), gives novel meaning to chemical control

Surface hydrophobicity of organisms provides biological self-protection. The hydrophobicity of pest surface, acting as a main obstacle for the pest control, can lead to low utilization and high loss of pesticides. Dermanyssus gallinae is a notorious pest in egg-laying hens, whose control primarily depends on acaricide spraying, while its surface hydrophobicity and potential influence on pesticide effectiveness are not clear. In the present study, the contact angle measurements revealed that the surface of D. gallinae was hydrophobic. Analysis using scanning electron microscopy (SEM) and transmission electron microscopy (TEM) showed that the surface microstructures of D. gallinae consist of cuticular folds, with a lipid-rich outermost layer of the cuticle. Based on gas chromatography-mass spectrometry (GC-MS) and gas chromatography (GC), it was found that the major compositions of cuticular lipids were fatty acids and n-alkanes. Modifying the chemical compositions and microstructures of the D. gallinae surface resulted in a reduction in surface hydrophobicity and an increase in the permeation of Rhodamine B through the cuticle. This observation suggested that the chemical compositions and microstructures were pivotal in determining surface hydrophobicity, hindering compound penetration into the cuticle. Finally, it was found improving the wettability of pesticide solution by adding surfactants could overcome the surface hydrophobicity and enhance the efficacy of pesticide against the mites. This study sheds light on the surface hydrophobicity mechanism of D. gallinae and provides a novel strategy to improve the efficacy of acaricides against the mites.

Emerging magnetic-responsive hydrogel actuators with anisotropic shape for intracardiovascular directional motion

A magnetically responsive valve actuator inspired by the starfish shape and fabricated with hydrophilic and hydrophobic surfaces was developed. The surface morphology and wettability of the magnetically responsive colloidal crystal hydrogel actuator were characterized using scanning electron microscopy and contact angle measurements. The actuator, resembling a flower, consists of Poly(HEMA-co-AAm)/Fe3O4/PDMS, exhibiting distinct Janus wettability with hydrophobic Fe3O4/PDMS and hydrophilic Poly(HEMA-co-AAm) surfaces. The directional movement of water droplets on the V-shaped structured film confirmed the anisotropic wetting behavior, influenced by the film’s wettability and structural dimensions. Moreover, the actuator demonstrated responsive angular and positional adjustments under varying magnetic fields, facilitated by embedded Fe3O4 particles aligning with magnetic lines of force. In experimental setups simulating intravascular applications, the actuator exhibited controlled movement within tubes and demonstrated effective adhesion to heart valve injuries under magnetic guidance. Additionally, a layered inverse opal film within the actuator showed promising capabilities for unidirectional fluid permeation, enhancing its functional versatility. These findings underscore the potential of the magnetically responsive colloidal crystal hydrogel actuator for biomedical applications, particularly in minimally invasive cardiac interventions requiring precise actuation and adhesive functionalities.

Synergistic adsorption mechanism of novel combined collector in flotation separation of fayalite from magnetite: Experiments and MD simulations

As an iron-bearing silicate mineral, fayalite has similar surface properties to magnetite, which makes it challenging to efficiently separate fayalite from magnetite by flotation. In this study, magnetite and fayalite were separated using novel combined collector polyoxyethylene alkyl amine (PAE) and terpinol (AT) through reverse flotation. Combined with a variety of characterization analysis and molecular dynamics (MD) simulation, the synergistic adsorption mechanism of the combined collector on mineral surface was revealed from multiple perspectives. The optimum scheme and pH response range of the combined collector were determined by micro-flotation test. Compared with PAE alone, the difference value of flotation recovery between fayalite and magnetite using combined collector was increased by 10.16%, and the dosage was reduced by 20%. Additionally, an effectively adsorption of combined collector onto fayalite surface to improve its surface hydrophobicity. Fourier transform infrared (FTIR), X-ray photoelectron spectroscopy (XPS) and MD simulations results showed synergistic adsorption was produced onto fayalite surface using combined collector mainly through non-polar interaction, hydrogen bond association and bridge adsorption. Furthermore, the spatial distribution and diffusion behavior of water molecules provide microscopic evidence for the enhancement of surface hydrophobicity of fayalite by combined collector.

Preparation of the sandwiched PS-SiO2-PVAc-SiO2 electrospinning fiber membrane with super-hydrophobic and self-cleaning and its performance in oil-water emulsion separation

Oil-water emulsion separation could improve the efficiency of oil resources and reduce environmental pollution. The efficiency of oil-water separation was directly affected by the surface hydrophobicity of the membrane and its reliability and reusability. Therefore, the construction of a reliable and reusable super-hydrophobic surface was very important. In this research, the EFM with sandwich structure of PS-SiO2-PVAc-SiO2 was easily fabricated by a three times liquid phase induction process and heat treatment. The PS-SiO2-PVAc-SiO2 EFM was first formed by a triple liquid phase induction process, then the EFM was heat-treated, the PVAc, which is a heat-sensitive material, resulting in SiO2 nanoparticles being welded onto PS fibers. The rolling contact angle experiment at an inclination of 8° proved that the PS-SiO2-PVAc-SiO2 EFM has super-hydrophobic properties. Meanwhile, the PS-SiO2-PVAc-SiO2 EFM showed excellent stability and reliability of super-hydrophobic properties after the EFM was washed or taped. In addition, the PS-SiO2-PVAc-SiO2 EFM had self-cleaning function and fine oil-water separation property. The oil-water separation efficiency was over 99.50 % and the flow rate was 68 L/m2h. After 5 times of oil-water separation, the flux and separation efficiency did not decrease significantly, which proved that the PS-SiO2-PVAc-SiO2 EFM could be reusable.

Vibration-Induced Pancake Bouncing of Impacting Droplets on Hydrophobic Surfaces.

Rapid detachment of impacting droplets from solid surfaces is fundamentally interesting and important in many practical applications, including self-cleaning, anti-icing, and energy harvesting. The droplet pancake bouncing is strongly preferred for the reduced contact time and high bouncing velocity. However, the trigger conditions for pancake bouncing are rigorous. Driven by this, this work circumvents the limitations via solid surface vibration. Our results show that the impacting droplet patterns are highly sensitive to the surface vibration parameters (i.e., the vibration amplitude and frequency), and only a reasonable design of vibration parameters enables the impacting droplets to bounce in a pancake shape without the contraction stage. Intriguingly, the pancake bouncing induced by surface vibration exhibits a significant reduction of solid-liquid contact time (up to ≈80%) compared to the traditional bouncing pattern, and the bouncing velocity has been dramatically enhanced. Furthermore, the critical conditions for the pancake bouncing on the hydrophobic surface and the underlying dynamic mechanism are also identified. This work provides an effective method to achieve well-controlled pancake bouncing of impacting droplets for extensive applications.

Impact of laterally mobile surface charge on diffusiophoresis of hydrophobic rigid colloids

The diffusiophoresis of charged hydrophobic nanoparticles (NPs) governed by an imposed ionic concentration gradient is analysed. The main objective is to elucidate the impact of the laterally mobile adsorbed surface ions at the interface on the propulsion of the hydrophobic NPs in diffusiophoresis. In addition, the dielectric polarization due to the difference in dielectric constant between the NPs and the suspension medium is also considered. The mobile surface ions create a friction as well as an electric force at the hydrophobic surface, which leads to a modification of the slip velocity condition and the slip length. We obtain an exact numerical solution of the governing electrokinetic equations in their full form by adopting a control volume formulation. The numerical model is supplemented by analytical solutions derived based on the Debye–Hückel linearization. We find that the lateral mobility of the surface ions obstruct the coions to diffuse from the higher concentration side to the lower concentration side, which results in a repulsive force to the particle leading to the occurrence of a negative mobility. Based on the numerical results and analytical solutions, we have shown that for a fully mobile surface charge, the diffusiophoresis of a hydrophobic NP is identical to the diffusiophoresis of a liquid droplet whose viscosity is related to the slip length of the hydrophobic particle. We establish that the dielectric polarization enhances the velocity of a hydrophobic particle, which has potential applications in the practical context.

Dual modification of the aggregation behavior and in vitro digestion of oxidized pine kernel protein via a combination of homogenization and succinylation

Protein oxidation affects the high-value utilization of nuts as oxidative attack causes protein aggregation, thereby challenging their technological functionality. Herein, a strategy using homogenization-assisted octenyl succinic anhydride (OSA) modification was proposed to tailor the structure, aggregation behavior, and digestive characteristics of oxidized pine kernel proteins. Results indicated that the ratio of α-helices to β-turns ranged from as low as 0.43 up to 0.67 after homogenization, suggesting greater molecular flexibility. With increasing protein oxidation, the acylation degree exhibited an inverted V-shaped trend, peaking at 67.22 %. OSA treatment reduced the aggregation rate and prolonged the lag time of proteins by stabilizing the α-helices and β-turns, increasing hydrogen bonding, and decreasing hydrophobicity. This increased the solubility of oxidized pine kernel proteins by ~30 % and improved their fluidity and thermal stability. A lower degree of succinylation was associated with higher free sulfhydryl content and surface hydrophobicity, which facilitated the thermal aggregation and the formation of elastomeric gels. Furthermore, the in vitro dynamic digestion and morphological observations of hydrolysis products indicated that cotreated proteins exhibited higher digestibility and formed small spherical particles ranging from 405.50 to 676.50 nm. These findings provide a promising approach to mitigate the adverse effects of oxidation on nut proteins.

Computer-Aided Site-Specific PEGylation of PET Hydrolases for Enhanced PET Degradation.

The enormous accumulation of poly(ethylene terephthalate) (PET) waste has posed a serious threat to the environment and human health, and biodegradation with PET hydrolase (PETase) can be a possible solution. Herein, we propose site-specifically modifying PETase with amphiphilic polymers to improve the enzyme performance at ambient temperature. For this purpose, we devise a computer-aided strategy to prioritize the conjugation site, and polyethylene glycol (PEG) preparations of 0.55 to 10 kDa are site-specifically conjugated to PETase. The most active conjugate PETase-PEG 5k (PETase-5K) shows an increase of melting temperature (3.88 °C) and significantly improves PET degradation performance (3.5- and 3.1-fold increases at 30 and 40 °C, respectively). Experimental investigation and molecular dynamics simulations reveal that the site-specific PEGylation increases the hydrophobic solvent-accessible surface area and the binding capability to the PET surface, thickens the hydration layer, increases the intramolecular hydrogen bonding, reduces the interactions between water and the conjugated enzyme surface, and rigidifies the enzyme structure via hydrogen bonding and hydrophobic interactions between the polymer and the enzyme, thus leading to improved enzymatic performance of PETase-5K. We further validate the versatility of the site-specific PEGylation in one of the most evolved variants of PETase, FAST-PETase, by 1.8-fold improvement in PET degradation at 30 °C. The presented computer-aided site-specific conjugation strategy has opened a new avenue to enhancing PETase performance at ambient temperature, and the contribution of PEGylation to PETase unraveled in this work laid a foundation for the rational engineering of PET hydrolases.

Typical Heterotrophic and Autotrophic Nitrogen Removal Process Coupled with Membrane Bioreactor: Comparison of Fouling Behavior and Characterization.

There is limited research on the relationship between membrane fouling and microbial metabolites in the nitrogen removal process coupled with membrane bioreactors (MBRs). In this study, we compared anoxic-oxic (AO) and partial nitritation-anammox (PNA), which were selected as representative heterotrophic and autotrophic biological nitrogen removal-coupled MBR processes for their fouling behavior. At the same nitrogen loading rate of 100 mg/L and mixed liquor suspended solids (MLSS) concentration of 4000 mg/L, PNA-MBR exhibited more severe membrane fouling compared to AO-MBR, as evidenced by monitoring changes in transmembrane pressure (TMP). In the autotrophic nitrogen removal process, without added organic carbon, the supernatant of PNA-MBR had higher concentrations of protein, polysaccharides, and low-molecular-weight humic substances, leading to a rapid flux decline. Extracellular polymeric substances (EPS) extracted from suspended sludge and cake sludge in PNA-MBR also contributed to more severe membrane fouling than in AO-MBR. The EPS subfractions of PNA-MBR exhibited looser secondary structures in protein and stronger surface hydrophobicity, particularly in the cake sludge, which contained higher contents of humic substances with lower molecular weights. The higher abundances of Candidatus Brocadia and Chloroflexi in PNA-MBR could lead to the production of more hydrophobic organics and humic substances. Hydrophobic metabolism products as well as anammox bacteria were deposited on the hydrophobic membrane surface and formed serious fouling. Therefore, hydrophilic membrane modification is more urgently needed to mitigate membrane fouling when running PNA-MBR than AO-MBR.

Ultrasonic-Assisted Marine Antifouling Strategy on Gel-like Epoxy Primer

Ultrasonic technology has drawn extensive interests for its great potential in marine antifouling applications. However, its effects on the adhesion behavior of marine fouling organisms on marine structures remain underexplored. This work investigated how ultrasonic treatment impacted the adhesion of Pseudoalteromonas on a gel-like marine epoxy primer. And the process parameters for ultrasonic treatment were optimized using response surface analysis with Design-Expert software 11. The results revealed that ultrasonic treatment disrupted the cellular structure of Pseudoalteromonas, causing the deformation and fragmentation of the cell membrane, leading to bacterial death. Additionally, ultrasonic treatment reduced the particle size and Zeta potential value of Pseudoalteromonas, which disrupted the stability of bacterial suspensions. It also increased the relative surface hydrophobicity of Pseudoalteromonas cells, resulting in a reduction in adhesion to the gel-like marine epoxy primer. This study demonstrated that ultrasonic treatment significantly disturbed the adhesion behavior of microorganisms like Pseudoalteromonas on the gel-like marine epoxy primer, which provided an effective approach for controlling marine biofouling.

Structure-property relationship of pea protein microgels as fat analogues in Pickering oil-in-water emulsions: effect of salt addition.

The design of plant-based microgels provides a platform for food ingredients to enhance palatability and functionality. This work aimed to explore the modifying effect of salt addition (KCl) on the structure of pea protein microgel particles (PPI MPs), on the interfacial adsorption and characteristics of formed emulsions as fat analogues. Salt addition (0-200 mmol L-1) promoted a structural transformation from α-helix to β-sheet, increased the surface hydrophobicity (from 1160.8 to 2280.7), and increased the contact angle (from 56.73° to 96.47°) of PPI MPs. The electrostatic shielding effect led to the tighter packing of MPs with irregular structures and lowered the adsorption energy barrier. Notably, salt-treated PPI MPs could adjust their adsorption state at the interface. The discernible adsorption of PPI MPs with 200 mmol L-1 salt addition that possessed enhanced anti-deformation ability dominated the interfacial stabilization, whereas a relatively rougher stretched continuous interfacial film formed after spreading and deformation of 0 mmol L-1 MPs. A tribological test suggested that emulsion stabilized by MPs at 0 (0.0053) and 80 mmol L-1 (0.0068) had similar friction coefficients to commercial mayonnaise (0.0058), whereas a higher salt concentration (200 mmol L-1) lowered its oral sensation due to the adsorption layer and enhanced the resistance to droplet coalescence during oral processing. Salt could be a modifier to tune the structure of microgels, and further promote the formation and attributes of emulsions. This study would improve application attributes of PPI MPs in the design of realistic fat analogues. © 2024 Society of Chemical Industry.

Synthesis, structural characterization, thermal analysis and anticorrosion properties of novel AZO-based imidazo[1,2-a]pyridine derivatives: Experimental study and theoretical approaches

In this study, innovative AZO-based imidazo[1,2-a]pyridine derivatives were synthesized using simple and efficient synthetic approach enabling large-scale production. Thermal analysis highlights their suitability for potential applications requiring resistance to moderate temperatures. These compounds were investigated as corrosion inhibitors for MS in a 1 M HCl-medium. Corrosion inhibition studies, including weight loss, PotentioDynamic polarization and electrochemical impedance spectroscopy methods, revealed that AZOs exhibited maximum corrosion inhibition efficiencies reaching 96.13 % and 94.07 %, respectively, at a concentration of 10−3 M and a temperature of 298 K, with both compounds acting as mixed-type inhibitors. The study also delved into the influence of temperature and immersion time on inhibitory performance, revealing stable inhibition within the temperature range of 298–328 K. The calculated standard free energy of adsorption was −42.06 and −40.62 kJ/mol for AZO 1 and AZO 2, respectively, suggesting mixed-type adsorption, with adsorption behavior following the Langmuir isotherm. Morphological analysis through SEM and AFM, showed a reduction in surface roughness in the presence of the inhibitors, while water contact angle measurements indicated a significant increase in surface hydrophobicity. UV–visible and FT-IR analyses confirmed the interaction of AZOs with the MS surface, suggesting the formation of a protective layer composed of adsorbed AZO molecules. Furthermore, computational investigations employing DFT, Monte Carlo, and Molecular Dynamic simulation revealed the formation of coordinate bonds between the studied inhibitors and the metal surface, confirming adsorption on the metallic surface. These findings align well with experimental outcomes, and a possible corrosion inhibition mechanism process was discussed.