Reduction In Contact Angle Research Articles

Methane seepage leads to a specific microplastic aging process in the simulated cold seep environment

Marine microplastics pose a significant threat to ecosystems, and deep-sea regions serve as critical sinks for these pollutants. Among these regions, cold seeps harbor relatively high concentrations of microplastics. However, research on the aging of microplastics under low-temperature, dark, methane-abundant, and high-pressure conditions remains limited. Seawater and sediment were collected from various Haima cold seepage sites to simulate seepage environments in 200-mL high-pressure reactors. Four types of microplastics at high concentrations (approximately 10 %) were cultured and monitored over two months to explore how they aged. The key findings are as follows: (1) Compared to areas of weak seepage, methane seepage accelerated microplastic aging, as evidenced by increased surface roughness, enhanced C-O and (CO)-O bond formation, increased microbial colonization, and reduced contact angles. (2) Microplastic aging is more pronounced in sediments than in seawater, with biodegradable polylactic acid (PLA) exhibiting the most significant aging characteristics and carbon contribution. (3) Aged microplastics induce greater disturbances in inorganic nutrient levels than in organic matter, impacting nitrogen cycle processes involving nitrate, nitrite, and ammonium. This study results reveal the fundamental aging characteristics of microplastics in extremely deep seas and highlight their potential ecological effects.

Separation properties and fouling resistance of polyethersulfone membrane modified by fungal chitosan

This research explores the enhancement of polyethersulfone (PES) membranes through the incorporation of chitosan derived from the lignicolous fungus Ganoderma sp. Utilizing wet phase inversion and solution casting techniques, chitosan was successfully integrated into the PES matrix, as confirmed by Fourier Transform Infrared Spectroscopy (FT-IR), which indicated a high deacetylation degree of 75.7%. The incorporation of chitosan significantly increased the membrane hydrophilicity, as evidenced by a reduction in the water contact angle and a substantial improvement in pure water permeability, from 17.9 L m-2 h-1 bar-1 to 27.3 L m-2 h-1 bar-1. The membrane anti-fouling properties were also notably enhanced, with the Flux Recovery Ratio (FRR) increasing from approximately 60–80%. Moreover, the chitosan-modified PES/CS membrane, particularly at a 5% chitosan concentration, demonstrated exceptional efficacy in pollutant removal, achieving over 90% elimination of total suspended solids, cadmium (Cd), and lead (Pb), alongside a 79% reduction in color during the treatment of textile wastewater.

Emulsifying properties of quinoa protein fibrillar aggregates and their influence on quinoa protein emulsion gel formation

Fibrillization is a potential way to improve functionality of seed storage proteins. Herein, the solubility, morphology, wettability, interfacial adsorption and emulsifying properties of quinoa protein fibrillar aggregates were compared with those of quinoa protein isolate (QPI). Effect of fibrillar aggregates on the formation of heat-induced QPI emulsion gels was investigated in the presence 0 or 100 mM NaCl. The results showed that fibrillization enhanced relative solubility of QPI by ~10 %, and reduced contact angle from 130.5° to 83.4°. Both QPI and fibrillar aggregates exhibited outstanding emulsifying capacity and emulsion stability against flocculation/coalescence. The interfacial protein concentration of fibrillar aggregate-stabilized emulsions was higher than that of QPI-stabilized emulsions, ranging from 16.3 to 33.4 vs. 12.4 to 29.2 mg/m2 at emulsifier concentrations of 0.5–3 % w/w. The self-standing emulsion gels were formed by heating 10 % w/w QPI emulsions with the storage modulus of 1886 Pa and the fracture stress of 582 Pa. Fibrillar aggregates acted as active fillers in QPI emulsions gels (8 % w/w QPI + 2 % w/w fibrillar aggregates) with the storage modulus of 2566 Pa and the fracture stress of 741 Pa. The addition of 100 mM NaCl destructed the gel network, leading to a reduction of gel strength.

Glass Surface Nanostructuring by Soft Lithography and Chemical Etching.

Due to its high durability and transparency, soda lime glass holds a huge potential for several applications such as photovoltaics, optical instrumentation and biomedical devices, among others. The different technologies request specific properties, which can be enhanced through the modification of the surface morphology with a nanopattern. Here, we report a simple method to nanostructure a glass surface with soft lithography and wet-chemical etching in potassium hydroxide (KOH) solutions. Glass samples etched with a polymeric mask showed a nanopattern with stripes of widths between 220 and 450 nm and modulated heights between 50 and 200 nm. For different solution concentrations or etching times, the obtained nanopatterns led to an increase or reduction of the water contact angle. The largest increment, ~20 degrees, was achieved by etching the glass for 180 min with 30% KOH concentration, while a super-hydrophilic glass (~9° contact angle) was achieved when etching for 90 min with the same concentration. Optical characterization showed a very low influence of the nanostructured pattern on glass transparency and an increment in UV transmittance for some cases.

Chemical enhanced oil recovery using carbonized ZIF-67 MOFs and sulfonated copolymers at high reservoir temperatures

Traditional nanoparticle and polymer-based enhanced oil recovery methods face challenges such as nanoparticle agglomeration and polymer adsorption, particularly at elevated reservoir temperatures. This study introduces hybrid polymeric nanofluids, combining carbonized Zeolitic Imidazolate Framework-67 (ZIF-67) with sulfonated copolymers to address these issues. Viscosity tests were conducted at 25 °C, 50 °C, 75 °C, and 90 °C, revealing a 39.67 % increase in viscosity at 90 °C, attributed to electrostatic and hydrogen bond interactions. For subsequent analyses—stability, adsorption, and core flooding—75 °C was selected as the representative high reservoir temperature. Stability assessments, confirmed via UV–Vis spectroscopy, demonstrated nanofluid durability over at least seven days. Carbonized ZIF-67 reduced polymer adsorption on rock surfaces, enhancing oil recovery and reducing environmental impact. Dynamic core flooding experiments showed a 45.8 % improvement in oil recovery by the hybrid nanofluid on carbonate rock samples. The hybrid nanofluid increased RF and RRF, improving the mobility ratio and redirecting flow to lower-permeability zones, reducing unswept oil and enhancing macroscopic sweep efficiency. Winsor Type III emulsification during the post-flooding phase of polymer-nanoparticle injection significantly improved trapped oil mobilization. Reduced contact angles from 170° to 100° altered the wettability, enhancing oil recovery. Carbonized ZIF-67 nanoparticles increased viscous forces, reduced capillary forces, and minimized polymer adsorption. The polymeric nanofluid achieved a capillary number of 1.0 × 10−3, two orders higher than that of polymer alone, resulting in superior performance. Injectivity optimization showed shear rates of 15.9 s−1 in 1700 mD cores and 79.8 s−1 in 80 mD cores, causing pressure drops of 15 psi and 1200 psi, respectively. This highlights injectivity challenges in 80 mD cores, while cores ≥ 290 mD are ideal for our polymer-nanoparticle hybrid applications.

Photocatalysis, wettability and optical properties of N-doped Cu2O/CuO thin films for smart coating applications

Abstract Undoped and nitrogen (N)_doped Cu2O/CuO thin films were deposited via reactive DC magnetron sputtering. The deposition was carried out by sputtering the Cu targets under various Ar/N2/O2 gas flow ratios. The structural, optical, wettability, and photocatalytic performance of the deposited films were investigated. A simple cubic Cu2O crystallographic phase is observed for the undoped film, whereas mixed cubic Cu2O and monoclinic CuO phases (Cu2O/CuO) are observed for the N_doped films. EDAX revealed that as the N2 flow rate increased the amount of nitrogen incorporated into the film increased. The transmittance and reflectance are affected by the incorporation of nitrogen into the films. The transmittance values decreased with increasing N2 flow rate, whereas the reflectance values increased. Both the refractive index and extinction coefficient almost increased with increasing N2 flow rate. A noticeable optical band gap narrowing from 2.55 eV to 2.39 eV was detected upon increasing the N2 flow from 0.0 to 190 sccm. The photoluminescence spectrum of the undoped sample contains five distinct bands at 518, 612, 654, 714 and 825 nm. These five maxima are attributed to the radiative decay of bound and free excitons, and oxygen vacancies (VO) After nitrogen incorporation, the photoluminescence intensity decreases and then increases again with increasing N2 flow rate. A reduction in the water contact angle was observed with increasing N2 flow rate. Upon Vis-light illumination, the N_doped Cu2O/CuO films reached superhydrophilicity faster than the undoped film did. The photocatalytic performance of the deposited Cu2O/CuO films was strongly enhanced with a small amount of N doping. The deposited films are promising for self-cleaning and photocatalytic degradation of organic wastes.

Surface modification of carbon fibres via plasma-activated water for mitigating burnout risk from direct plasma treatment

This study presents a novel plasma jet discharge device designed to indirectly treat carbon fibre materials with plasma-activated water. This innovative method effectively mitigates issues related to carbon fibre conduction and combustion, which are common challenges encountered when directly modifying fibres using a plasma jet. Specifically, the atmospheric composition is adjusted to modulate the active particles in the liquid phase. The experimental results demonstrate that this technique significantly increases the surface wettability of carbon fibres without damaging their structure. Under the conditions of argon/oxygen cascade discharge, oxygen-containing substances generate ionomers that activate the water, which in turn introduces oxygen-containing groups (e.g., C−O, C=O, O−C=O) onto the carbon fibre surface. These groups catalyse monomer polymerisation on the material surface, which increases the wettability of the carbon fibres, as evidenced by a significant reduction in the water contact angle from 80.12° to 55.31°. This in turn improves the bonding strength with epoxy resin and slightly increases the monofilament strength. Furthermore, composites produced by this method exhibit 21% higher interlaminar shear strength than the untreated sample and an increased O/C ratio of up to 24.55%. In summary, these findings provide a valuable theoretical basis for enhancing the surface properties of carbon fibre composites through plasma–liquid interactions and open new possibilities for high-performance carbon fibre–resin matrix composites.

Development of two layer fibrous scaffolds for 3D in vitro modelling: Effects of morphology and surface properties on cell proliferation, adhesion and drug sensitivity

Three-dimensional (3D) in vitro cell models are gaining popularity in cancer research compared to two-dimensional (2D) cell culture models because of their ability to more accurately represent the tissue microenvironment. This study introduces a novel approach for the fabrication of 3D cell culture models by combining modified melt-electrospinning technology and solution electrospinning to create 3D two-layer fibrous scaffolds. By manipulating electrospinning parameters (voltage 11–12 kV and feed rate 0.85–1.55 mg/min), we engineered poly (ε-caprolactone) (PCL) scaffolds with varying fiber diameters (8.9 ± 2.2 to 23.1 ± 3.4 μm) and pore sizes (32.7 ± 12.8 to 122.5 ± 21.1 μm). Non-thermal plasma (NTP) treatment at energy density of 0.23 J/cm2 enhanced surface hydrophilicity, evident in a significant reduction in water contact angles from 113 ± 0° to 64 ± 0°. A comprehensive set of characterization techniques, including X-ray diffraction (XRD), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA) confirmed that plasma treatment altered the surface wettability without compromising the scaffold's chemical stability or crystalline structure. Biological assays involving human breast cancer MDA-MB-231 cells and human glioblastoma U-87 MG cells demonstrated high cell viability, indicating biocompatibility of the scaffolds. A pronounced difference in proliferation patterns was noted between MDA-MB-231 and U-87 MG, with the latter fully utilizing voids for the formation of cell aggregates, especially in the “fine” scaffold, indicating the dependence of cell behavior on scaffold architecture, which must be adjusted according to the modelled system and duration. Furthermore, investigation of the therapeutic efficacy of doxorubicin revealed a distinct drug response in 3D cultures, EC50 values of doxorubicin in 3D culture was approximately twice higher compared to 2D. These findings underscore the potential of tailored PCL scaffolds to create more physiologically relevant models for cancer research, tissue engineering, and drug screening applications, highlighting the necessity for careful consideration of scaffold design to achieve the desired in vitro model.

Thermal hysteresis in wettability and the Leidenfrost phenomenon

The Leidenfrost temperature (TL), at which the liquid drop lifetime peaks on a superheated surface, is believed to be wettability dependent. Here, we show that the wettability effect on TL is subject to the history of the surface temperature. Observing a water drop evaporating on a polished stainless-steel surface heated from 100 to 400∘C in argon gas, we find TL≈265∘C. We then repeat the experiment along decreasing temperature and find a TL increase by 10 K, i.e., TL≈275∘C. This thermal hysteresis is due to a reduced contact angle during heating. Once hydrophilized, the hysteresis disappears until the contact angle recovers. Similar observations are made in the air where oxidation is possible. Published by the American Physical Society 2024

Redox-Responsive Nanopesticides Based on Natural Polymers for Environmentally Safe Delivery of Pesticides with Enhanced Foliar Dispersion and Washout Resistance.

Based on the modified cross-linking of the degradable natural polymers chitosan oligosaccharides (COS) and gelatin (GEL) via introduction of a functional bridge 3,3'-dithiodipropionic acid, this study constructed an environmentally responsive dinotefuran (DNF) delivery system (DNF@COS-SS-GEL). The introduction of the disulfide bond (-S-S-) endowed DNF@COS-SS-GEL with redox-responsive properties, allowing for the rapid release of pesticides when stimulated by glutathione (GSH) in the simulated insect. Compared with commercial DNF suspension concentrate (DNF-SC), DNF@COS-SS-GEL showed superior wet spreading and retention performance on cabbage leaves with a reduced contact angle (57°) at 180 s and 4-fold increased retention capacity after rainfall washout. Nanoencapsulation effectively improved the UV-photostability with only a 31.4% decomposition rate of DNF@COS-SS-GEL at 96 h. The small scale and large specific surface area resulted in excellent uptake and transportation properties in plants as well as higher bioactivity against Plutella xylostella larvae. This study will help promote sustainable agricultural development by reducing environmental pollution through improved pesticide utilization.

Chemical Oxidation-Induced Degradation in Gas Diffusion Layers for PEFC: Mechanisms and Performance Implications

Gas Diffusion Layers (GDLs) are integral in polymer electrolyte fuel cells, facilitating gas and water transport while providing structural support. However, their susceptibility to chemical degradation significantly impacts their functionality over extensive periods of time. This study investigates the mechanisms of GDL degradation, focusing on chemical oxidation. Accelerated stress testing, which involves immersing GDL in Fenton’s reagent for 24 h, is used. Ex-situ analysis reveals changes in surface properties, including a 3% reduction in contact angle, from 15% to only 9% remaining fluorine on the surface, and OH group presence in GDLs exposed to Fenton’s reagent. In-situ methods are used to study the impact of GDL degradation on fuel cell performance. Polarization curve reveals a 17% performance enhancement in aged GDLs, with a corresponding 19% decrease in voltage loss due to oxygen transport resistance at a high current observed via transient limiting current analysis. Electrochemical impedance spectroscopy reveals a 51% reduction in mass transport resistance, providing insights into structural alterations, such as pore widening and increased hydrophilicity. Despite these improvements, aged GDL demonstrates substantial degradation under high humidity, leading to water management challenges and voltage instability. This is attributed to the loss of fluorine, as indicated by the ex situ analysis.

A low-pollution surface modification system for improving the adhesion of polycarbonate

In the present study, the surface adhesion capacity of polycarbonate (PC) has been improved by using a low-pollution surface modification system that includes alkaline potassium ferrate (K2FeO4). The effects of environmentally friendly swelling conditions, NaOH and K2FeO4 contents, and other modification conditions on the PC surface topography, hydrophilicity, and surface roughness were then primarily studied. The modification resulted in an improvement of the hydrophilic property of the PC surface. There was a significant reduction in the surface contact angle from 97.6° to 34.1°. A considerable increase in the PC surface’s average surface roughness (Ra) was also observed, which increased from 2 nm to 209 nm. Meanwhile, after chemical copper plating, the maximum peel strength between the PC resin and copper layer reached 1.13 kN/m. Furthermore, infrared absorption spectroscopy (FT–IR) and X–ray photoelectron spectroscopy (XPS) was used in the analyses of the surface chemical structure of the PC substrate, both prior to and after surface treatments. The results indicated that the modification of the surface led to increased hydrophilic groups on the PC surface, which was advantageous for the subsequent PC treatments (involving chemical copper plating). In short, the PC surface modification increased surface roughness and surface hydrophilicity, which improved the bonding between the chemically plated copper layer and the PC substrate.

Native and TMT Chestnut Extractives as Hydrophobic and Photostabylizing Additives for Wood Surfaces

Wood extractives have proven strong anti-oxidative properties which may be used to mitigate surface deterioration caused by photolytic effects and free radical formations. An interesting challenge regarding wood extractives is understanding how they behave in terms of treating natural wood surfaces to reduce anti-oxidative processes that arise from exposure to the main environmental factors. In this study, the possible efficacy of chestnut (Castanea sativa Mill.) extractives derived from native (CH) and thermally modified wood (TMT CH), as a means of protecting against UV exposure in poplar (Populus spp.) and spruce (Picea abies Karst.) wood, was evaluated. Chestnut wood was first thermally modified at 180 °C for 3 h, and the extractives were obtained by the accelerated solvent extraction technique (ASE) and subsequently used to treat wood surfaces. Samples were immersed in extractive solutions and exposed to artificial UV-weathering exposure, then contact angle and colour stability were monitored during the process. An FTIR analysis of the photo-degradation process of poplar and spruce surfaces was also executed. Extractives of TMT chestnut changed the total colour variation in both poplar and spruce wood. A much darker colour compared to the extractives of native wood was observed and an increase in ∆E* from 9.75 to 30.76 and 6.24 to 22.97 in poplar and spruce was calculated. The stability of the colour depended both on the surface wood and the type of extractive. The initial contact angle remained almost unchanged in the poplar wood surface and only slightly increased in spruce regardless of whether they were treated with extractives from native or TMT chestnut wood. A strong reduction in contact angle after the accelerated UV exposure test was observed, especially in spruce treated with CH extractives. FTIR analysis confirmed the lower levels of chemical degradation of surfaces observed by colorimetry, where TMT CH extractives formed more stable chemical bonds than native extractives. The comparative analysis in this study clarified the complex relationships between the effects of high-temperature modification of wood and the potential protective role of TMT extractives on some wood surfaces.

In pursuit of sustainability in machining titanium alloys using phosphonium-based halogen-free ionic liquids as potential metalworking fluid additives

In recent years, researchers have investigated ionic liquids (ILs) as suitable metalworking fluids (MWFs) additive. Most commonly used ILs contain halogen anions, which creates issues related to corrosion and toxicity. However, phosphonium-based halogen-free ILs (HF-ILs) provide a safer alternate with enhanced biodegradability and minimal adverse effects on the environment. This research examines the potential of HF-ILs as an additive to canola oil. In this research two halogenated ILs [BMIM][PF6]- and [BMIM][BF4]- and one halogen-free IL ([P6,6,6,14][i(C8)2PO2]-) were added 1 % by volume in canola oil. First, the thermophysical properties of these synthesized MWFs were evaluated. Result concluded that the HF-ILs reduced contact angles on both the workpiece and the cutting tool surfaces by 12– 15 % compared to pure canola oil. Whereas, improved the thermal conductivity by 10.5 %. Furthermore, the machining operation was carried out at two cutting speeds (80 and 100 m/min) and feed (0.1 and 0.2 mm/rev) to analyse the effect of synthesized MWFs under the minimum quantity lubrication method. Findings concluded that phosphonium-based halogen-free IL showed better cutting performance, with reduction in tool wear, cutting temperature by 10–33 %, and surface roughness by 34−46 %. Additionally, this approach supports a "greener" and more sustainable work environment by lowering MWF consumption by using minimal quantity lubrication, reducing tool wear and surface roughness which helps in cost reduction and product rejection for any manufacturing industry.

Interactions of traditional and biodegradable microplastics with neonicotinoid pesticides

Neonicotinoid pesticides (NNPs) and microplastics (MPs) are two emerging contaminants in agricultural environment. However, the interaction between MPs (especially biodegradable plastics) and NNPs is currently unclear. Therefore, taking thiacloprid (THI) as an example of NNPs, this study explores the adsorption-desorption process and mechanism of NNPs on MPs (traditional and biodegradable plastics), and analyzed the main factors affecting the adsorption (pH, salinity and dissolved organic matter). In addition, by using diffusive gradients in thin-films device, this study assessed the impact of MPs on the bioavailability of NNPs in soil. The results showed that the maximum adsorption capacity of polyamide 6 (96.49 μg g−1) for THI was greater than that of poly (butylene adipate co-terephthalate) (88.78 μg g−1). Aging increased the adsorption amount of THI (5.53 %–15.8 %) due to the higher specific surface area and reduced contact angle of MPs, but the adsorption mechanism remained unchanged. The desorption amount of THI from MPs in simulated intestinal fluid is 1.30–1.36 times. The MPs in soil alter the distribution of THI in the soil, increasing the bioavailability of THI while inhibiting its degradation. The results highlighted the significance of examining the combined pollution caused by MPs and NNPs.

Silicon-infused bacterial cellulose: in situ bioprocessing for tailored strength and surface characteristics

In this study we investigate the use of in situ bioprocessing for the production and surface modification of bacterial cellulose (BC) with silicon additives. The surface properties and tensile strength of the BC were studied and compared with plain BC. The effect the modification exhibited on the survivability of the bacteria was assessed by optical density measurements and found that the addition of the modification marginally slowed growth in the case of Tetramethyl orthosilicate (TMOS) and did not affect the growth in the case of Tetraethyl orthosilicate (TEOS). Characterisation of the modified BC was carried out using FTIR, EDX and confirmed the presence of silicon in the material. The width of fibres in the microstructure of BC was measured using SEM. Two different silicon modifications were used to modify the BC, it was shown that the TMOS modification decreased the tensile strength but that the TEOS increased the tensile strength of the BC fibres compared to plain BC. In addition, we found that the washing conditions of 1% NaOH (w/v), industrial methylated spirit (IMS), and deionised water (DI) showed some impact on the properties of the samples, particularly the IMS produced a reduced contact angle in the modified samples. However, the contact angle increased in the case of TEOS modification with the NaOH wash. In conclusion this study shows a novel method of modifying BC materials in-situ using silicon additives for increased tensile strength and the potential for tuneable hydro interactions.

Performance of Chitosan/Carbon Nanotube-Coated Ultrafiltration Membranes for Natural Organic Matter Removal from Drinking Water

The objective of this study is to improve the filtration efficiency of commercially available polyethersulfone (PES) ultrafiltration (UF) membranes, with a specific focus on removing natural organic matter (NOM) and preventing membrane fouling. The modification of UF membranes was accomplished by utilizing chitosan/multi-walled carbon nanotubes (CS/MWCNT-OH) and employing both dip and spin coating techniques. The membrane surface morphologies were evaluated using the Attenuated Total Reflectance Fourier Transform Infrared Spectroscopy (ATR-FTIR), Scanning Electron Microscopy (SEM), Atomic Force Microscopy (AFM), and Energy-Dispersive X-ray Spectroscopy (EDX) techniques. Tests were carried out to assess the effectiveness of the membranes in a laboratory-scale system using two primary water sources from Istanbul, specifically the Melen River and Terkos Lake. Total organic carbon (TOC), UV254 absorbance, turbidity, and trihalomethane formation potential (THMFP) were all measured as part of a thorough analysis. The surface morphology investigations verified the effective deposition of MWCNT-OH nanoparticles onto the membrane surface. This was corroborated by the reduction in the water contact angle, showing an improvement in the hydrophilicity of the membrane. The modified membranes demonstrated much higher TOC removal rates compared to the original membranes. Specifically, the removal efficiencies for Melen River and Terkos Lake were 37.14% and 56.86%, respectively. Nevertheless, the alteration of the surface led to a decline in membrane flux as a result of the concurrent drop in pore size. To summarize, the results of this work highlights the considerable capability of surface modification using CS/MWCNT-OH to improve the performance and antifouling characteristics of commercial PES UF membranes.

Successful application of photocatalytic recycled TiO2-GO membranes for the removal of trace organic compounds from tertiary effluent

Photocatalytic membranes are a promising technology for water and wastewater treatment. Towards circular economy, extending the lifetime of reverse osmosis (RO) membranes for as long as possible is extremely important, due to the great amount of RO modules discarded every year around the world. Therefore, in the present study, photocatalytic membranes made of recycled post-lifespan RO membrane (polyamide thin-film composite), TiO2 nanoparticles and graphene oxide are used in the treatment tertiary-treated domestic wastewater to remove trace organic compounds (TrOCs). The inclusion of dopamine throughout the surface modification process enhanced the stability of the membranes to be used as long as 10 months of operation. We investigated TrOCs removal by the membrane itself and in combination with UV-C and visible light by LED. The best results were obtained with integrated membrane UV-C system at pH 9, with considerable reductions of diclofenac (92%) and antipyrine (87%). Changes in effluent pH demonstrated an improvement in the attenuation of TrOCs concentration at higher pHs. By modifying membranes with nanocomposites, an increase in membrane hydrophilicity (4° contact angle reduction) was demonstrated. The effect of the lamp position on the light fluence that reaches the membrane was assessed, and greater values were found in the middle of the membrane, providing parameters for process optimization (0.29 ± 0.10 mW cm−2 at the center of the membrane and 0.07 ± 0.03 mW cm−2 at the right and left extremities). Photocatalytic recycled TiO2-GO membranes have shown great performance to remove TrOCs and extend membrane lifespan, as sustainable technology to treat wastewater.

Influence of the Addition of TiO2 Nanoparticles on the Self-Cleaning Capacity of Cementitious Composites.

This study evaluated the potential of incorporating TiO2 nanoparticles (NT) into cementitious composites to provide self-cleaning and self-sanitising properties, as well as the partial replacement of natural aggregates with recycled glass (RGA), ceramic brick (RBA), granulated blast furnace slag (GBA), and textolite waste (RTA) from electronic equipment on these properties. Based on the research results, the addition of NT to cementitious composites led to a significant reduction in contact angle, which means an increase in surface hydrophilicity. At the same time, Rhodamine B stain fading was highlighted, with the degree of whiteness recovery of NT composites exceeding that of the control by up to 11% for natural aggregate compositions, 10.6% for RGA compositions, 19.9% for RBA compositions, 15% for GBA compositions, and 13% for RTA compositions. In a mould-contaminated environment, it was shown that the introduction of NT allowed the material to develop a biocidal surface capacity which is also influenced by the nature of the aggregates used. Furthermore, the study revealed that, under controlled conditions, certain recycled waste aggregates, such as textolite, promoted mould growth, while others, such as brick and slag, inhibited it, highlighting not just the effect of the addition of NT, but also the significant influence of the aggregate type on the microbial resistance of cementitious composites. These improvements in the performance of cementitious composites are particularly advantageous when applied to prefabricated elements intended for the finishing and decorative surfaces of institutional (schools, administrative buildings, religious structures, etc.) or residential buildings.

Tailoring silk fibroin hydrophilicity and physicochemical properties using sugar alcohols for medical device coatings

This study explores the modification of silk fibroin films for hydrophilic coating applications using various sugar alcohols. Films, prepared via solvent casting, incorporated glycerol, sorbitol, and maltitol, revealing distinctive transparency and UV absorption characteristics based on sugar alcohol chemical structures. X-ray diffraction confirmed a silk I to silk II transition influenced by sugar alcohols. Glycerol proved most effective in enhancing the β-sheet structure. The study also elucidated a conformational shift towards a β-sheet structure induced by sugar alcohols. Silk fibroin–sugar alcohol blind docking and sugar alcohol-sugar alcohol blind docking investigations were conducted utilizing the HDOCK Server. The computer simulation unveiled the significance of size and hydrogen bonding characteristics inherent in sugar alcohols, emphasizing their pivotal role in influencing interactions within silk fibroin matrices. Hydrophilicity of ozonized silicone surfaces improved through successful coating with silk fibroin films, particularly glycerol-containing ones, resulting in reduced contact angles. Strong adhesion between silk fibroin films and ozonized silicone surfaces was evident, indicating robust hydrogen bonding interactions. This comprehensive research provides crucial insights into sugar alcohols’ potential to modify silk fibroin film crystalline structures, offering valuable guidance for optimizing their design and functionality, especially in silicone coating applications.