Formation Of Monolayer Research Articles

Three-dimensional Culture of Buffalo (Bubalus bubalis) Mammary Epithelial Cell Line

Background: The mammary gland is a crucial organ in dairy animals, responsible for milk production, regulated by intricate hormonal and cellular interactions. Traditional two-dimensional (2D) cell culture systems used in mammary gland research fail to replicate the complex in vivo environment, limiting the understanding of mammary gland biology. The study explores the advantages of three-dimensional (3D) culture systems for Buffalo Mammary Epithelial Cells (BuMECs), aiming to enhance morphological and functional differentiation compared to 2D cultures. Methods: BuMECs were cultured in Dulbecco’s Modified Eagle’s Medium (DMEM/F12) supplemented with 10% FBS and specific growth factors. For 2D culture, BuMECs were grown on a plastic substratum. For 3D culture, cells were cultured on top of and embedded in growth factor-reduced (GFR) Matrigel. Morphological differentiation was observed under phase-contrast microscopy. Total RNA was extracted and cDNA was synthesized to measure β-casein gene expression using quantitative real-time PCR (qPCR). Protein expression was analyzed by Western blotting, targeting total casein. Result: BuMECs grown in 3D cultures exhibited enhanced morphological differentiation, forming alveolar and ductal structures, unlike the monolayer formation observed in 2D cultures. Rapid formation of duct-like structures was noted within 24 hours in 3D cultures. Functional differentiation was significantly improved, evidenced by a five-fold increase in β-casein mRNA expression and higher protein levels of α, β and κ-casein in 3D cultured cells compared to 2D cultures. Western blot analysis confirmed the elevated casein protein expression in 3D cultures.

Novel Efficient and Eco‐Friendly Biosorbent Derived from Ditax (Detarium senegalense) Fruit Hulls for Removal of Cationic Dyes: Adsorption Modeling and Statistical Optimization

AbstractRemediation of wastewater laden with dyes using optimized and less expensive techniques remains a challenge for environmental protection. In the current research work, alkaline activation approach was employed to derive a biosorbent from ditax fruit hulls (DS‐FHB), and its sorption performance was tested on Methylene blue (MB) dye biosorption with optimizing adsorption parameters. Structural and chemical properties of DS‐FHB including crystallinity, morphology, and surface functionality were analysed using XRD, SEM, FTIR technics, and pHPZC determination. Optimization of adsorption parameters using a centered composite design (CCD) from response surface methodology led to achieving a peak dye removal rate of 98.97 %. The optimal conditions were determined as DS‐FHB mass of 0.23 g, pH 7.12, contact time 39.00 min, and initial MB concentration of 69.35 mg/L. The findings demonstrated a strong alignment with both the Langmuir isotherm and pseudo‐second order kinetic model, suggesting their appropriateness in describing the adsorption process of MB onto DS‐FHB. According to the Langmuir isotherm model, the sorption of MB dye onto DS‐FHB occurred by monolayer formation with a maximum dye sorption capacity of 96.453 mg/g. Based on the structural and physico‐chemical properties of DS‐FHB biosorbent, and its adsoption applicability evaluated in the experimental conditions, detax derived‐biosorbent can be proposed as a successful and effective low‐cost biosorbent for removing cationic dyestuffs from aqueous solutions.

Large-Scale Formation of a Close-Packed Monolayer of Spheres Using Different Colloidal Lithography Techniques.

The possibility of using colloidal lithography at the industrial level depends on the ability to form defect-free coatings over large areas. The spin-coating method has not yet shown acceptable results, but a more detailed studying of the regularities of this process may improve the quality of masks. The Langmuir-Blodgett method is expected to be the most preferable for forming high-quality large-scale monolayers. Real-time controlling the surface pressure of the monolayer can allow to obtain close-packed arrays with long-range order. In this work, to develop the spin-coating technology, the influence of technological parameters (spin-coating speed and time, concentrations of components in suspension) on the substrate coverage area with a monolayer of polystyrene spheres (1.25 μm) was studied. An original automated Langmuir-Blodgett system was developed to study the influence of the monolayer surface pressure on its quality using polystyrene spheres (1.25, 1.8, 2.1 μm). The developed spin-coating technology resulted in a record coverage area (90%) of Si substrate (76 mm) and a defect-free hexagonally ordered domain area of 500 μm2. As a result of the developed Langmuir-Blodgett technique, a close-packed monolayer coating was obtained over the entire substrate area (coverage area 99.5%, defect-free domain area 3000 μm2) without the use of any surfactants.

Polycyclic aromatic hydrocarbon derivatives onto polar microplastics of polyurethane: equilibrium, thermodynamics, and kinetics of monolayer-multilayer adsorption.

The study of the adsorption of polycyclic aromatic hydrocarbons on microplastics (MPs) has attracted much attention as to how microplastics can act as carriers of these pollutants. Polyurethane (PU) is one of the MPs found in aquatic environments, containing different functional groups it can interact with polar and nonpolar molecules. PAH derivatives (dPAHs) present different properties and thus can be adsorbed by different interactions; thus, this study investigated the adsorption of fluorene (FLN), dibenzothiophene (DBT), dibenzofuran (DBF), and carbazole (CBZ) onto PU MP. The Langmuir, Freundlich, and BET isotherm models were examined, and the BET model best fitted. The adsorption was a nonspontaneous process, exothermic for mono- and multilayer formation for FLN, DBT, and CBZ, and endothermic for DBF monolayer formation. The adsorption monolayer was formed by van der Waals forces, H─bonding, and π─π interactions, while the formation of the multilayer can be explained by π─π and hydrophobic interactions. The pseudo-second-order model proved to be more consistent for the adsorption of dPAHs. The adsorption in artificial seawater shows no significant differences for the monolayer but favored the adsorption multilayer due to the salting-out effect. Due to the existence of several adsorption mechanisms, PU MP interacts with dPAHs in greater quantities when compared to a MP with a simpler structure.

Removal of sulphur and nitrogen compounds from model fuel by adsorption of modified activated carbon

This study aimed to achieve the highest percentage removal of dibenzothiophene (DBT), quinoline (QUI), and indole (IND) adsorbed by double-impregnated modified activated carbon (MAC). Modification of commercial activated carbon (AC) by sulphuric acid (H2SO4) of 15%, 30%, 45%, 60%, and 75% w/v followed by subsequent 1 zinc chloride (ZnCl2): 1 AC impregnation ratio and activated at 500 oC in a muffle furnace under self-generated atmosphere for an hour. The determination of optimized MAC was identified through the highest removal rate of DBT, QUI, and IND from adsorption experiments which were analysed using an ultraviolet-visible (UV-Vis) spectrophotometer. It was found that DBT and IND showed a removal high percentage of up to 86.23% and 82.77% respectively by using 75% H2SO4 with ZnCl2 MAC. Meanwhile, QUI favoured 30% H2SO4 with ZnCl2 MAC with a removal percentage of 33.17% which was still higher than unmodified AC. Physical and chemical properties such as the morphological structure, elemental analysis, porosity, pore size, surface functional group, percentage yield, pH, bulk density, content, ash content, and iodine number were studied for the optimized MAC. Scanning electron microscopy (SEM) and energy dispersive X-ray (EDX) spectroscopy and Fourier transform infrared spectroscopy (FTIR) were used to characterize the MAC. Both MACs showed high percentage yields of 72.08% and 71.13% for 30% and 75% H2SO4 and ZnCl2 MAC respectively. Meanwhile, the pH was between the ranges of 5.36-5.53 for both MACs. Bulk densities were also favourable while the moisture and ash content were within acceptable limits. Iodine numbers for 30% and 75% H2SO4 and ZnCl2 MAC were 857 and 861 mg/g respectively, hence indicating that the MAC achieved high porosity and good adsorption performance. Langmuir, Freundlich, and Temkin adsorption isotherm models as well as pseudo-first order (PFO) and pseudo-second order (PSO) kinetic models were considered for understanding the adsorption mechanisms. The study revealed that DBT, QUI, and IND removal processes, followed the Langmuir adsorption isotherm model with correlation coefficients, R2 of 0.9905, 0.9791, and 0.9964 respectively. Moreover, the adsorption kinetic data of DBT, QUI, and IND provided a better fitting to the PSO kinetic model with R2 of 0.9992, 0.9987, and 0.9998 respectively. According to the Langmuir isotherm model and PSO kinetic model, the adsorption mechanisms of DBT QUI and IND were chemisorbed under monolayer formations.

Ultrasonic assisted removal of methyl orange and bovine serum albumin from wastewater using modified activated carbons: RSM optimization and reusability

Abstract The removal of industrial pollutants from water remains a significant challenge in water treatment processes. This study investigated the efficacy of powder-activated carbon (PAC), thermally modified PAC (TPAC), and chemically modified PAC (CPAC) for removing bovine serum albumin (BSA) and methyl orange (MO) from simulated wastewater. After undergoing treatment, the BET surface area of TPAC increased to 823 m2/g, while that of CPAC increased to 657 m2/g compared to the initial surface area of pristine PAC, which was 619 m2/g. Batch adsorption experiments assisted by ultrasonication were conducted to evaluate the impact of solution pH, initial concentration, and contact time on the adsorption capacities (qmax) of BSA and MO. TPAC demonstrated superior performance, achieving qmax values of 152 mg/g for MO and 133 mg/g for BSA, compared to PAC, which provided qmax values of 124 mg/g and 112 mg/g for BSA, respectively. Furthermore, pH levels of 3 and 5 were identified as highly effective for the removal of MO and BSA from water, respectively. The adsorption kinetics of both MO and BSA followed pseudo2nd-order (R2 > 0.99) reaction kinetics under both batch and ultrasonic conditions, confirming the removal of contaminants through chemisorption. The adsorption trends also satisfied the Langmuir isothermal model, indicating the formation of a uniform monolayer during the adsorption process of these contaminants. To understand the simultaneous effect of all the variables, response surface methodology (RSM) using central composite design (CCD) was used to predict the adsorption capacities of CPAC. After five adsorption cycles, the removal efficiencies of MO (from 98% to 80%) and BSA (from 55% to 40%) decreased in the CPAC system. The results suggested that CPAC can be effectively utilized to remove MO from wastewater.

Modified Mg/Fe layered double hydroxide nanosheets as an efficient solar photocatalyst for hydrogen production from ammonium phosphate

Mg/Fe layered double hydroxides (LDHs) modified with Cu and W support were synthesized by a one-pot coprecipitation method. The resulting samples were extensively characterized using TGA, XRD, UV, FTIR, SEM, EDX, TEM, and N2 adsorption-desorption techniques. Finally, the calcined LDHs were evaluated for photocatalytic hydrogen production from triammonium phosphate-water solution under solar light irradiation. The XRD results demonstrated that all as prepared LDH samples had characteristic hydrotalcite phase and validated the formation of a well-crystallized layered structure. After calcination, the LDHs exhibited a sintered, broken-down morphology with 8–40 nm particles. The adsorption-desorption isotherms of the calcined LDHs were categorized as type IV with H3–H2 hysteresis, suggesting condensation capillarity and monolayer formation. The band gap values were 1.5 eV for Mg/Fe, 2.4 eV for Cu/Mg/Fe, and 2.8 eV for W/Mg/Fe calcined LDHs. In hydrogen evolution experiments, the Mg/Fe catalyst showed the highest volume of 45.3 ml, followed by Cu/Mg/Fe (43.7 ml) and W/Mg/Fe (40.1 ml). This was attributed to the higher BET surface area of 172 m2/g for Mg/Fe compared to 38 m2/g for W/Mg/Fe and 14 m2/g for Cu/Mg/Fe, enabling better distribution of active sites.

Comparative study of un-doped CeO2 and metal (Mn, Co, Fe)-doped CeO2 nanostructures for the removal of golden yellow dye from synthetic wastewater

ABSTRACT In this study, the activity of un-doped cerium oxide (CeO2) nanostructure with metal (Mn, Co, Fe)-doped CeO2 nanostructures was compared as effective scaffolds for the elimination of Golden Yellow (GY) Dye. For this purpose, the un-doped and doped-CeO2 nanostructures were prepared through co-precipitation treatment and characterised using the following techniques like FTIR, XRD, UV, PL, SEM and EDX analysis. The synthetic nanostructures were selected for the removal of GY through adsorption and photocatalytic degradation from wastewater. Tauc’s model was employed to determine the optical band gap, and various key parameters (contact duration, pH, nanostructure dosage and GY concentration) were optimised for the adsorption/photocatalytic degradation of GY. The adsorption and degradation processes for these nanostructures were found to be pH-dependent, with an optimum pH value of 4. UV–visible spectroscopy was employed to probe the GY adsorption followed by the GY degradation, revealing a higher removal and degradation efficiency of 39.89% and 58.46% for Mn-CeO2, 34.60% and 47.21% for Co-CeO2 and 31.67% and 39.10% for Fe-CeO2 compared to 14.05% and 30.37% for un-doped CeO2, respectively. In total, 98.35% of GY removal was achieved by Mn-CeO2 compared to 44.42% by un-doped CeO2 within 175 min via adsorption (50 min) followed by degradation (125 min). Additionally, the absorption mechanism underwent analysis, with the kinetic data aligning closely with the pseudo-first-order model. Examination of the adsorption capacity at various equilibrium concentrations of the dye solution revealed the formation of monolayers and chemisorption phenomena. Moreover, the rate constant dropped when scavengers like ethylenediaminetetraacetic acid (EDTA), isopropyl alcohol (IPA), and hydrogen peroxide (H2O2) were added because they capture holes (h+), hydroxyl radicals (·OH), and superoxide radicals (·O2 −) respectively, with EDTA showing more prominent effects.

Novel mixed self-assembled monolayers of L-cysteine and methanol on gold surfaces under ambient conditions.

In this work, we carried out an experimental and theoretical study on the formation of self-assembled monolayers of L-cysteine molecules on gold surfaces in the presence of methanol as a solvent. We report for the first time L-cysteine and methanol ordered structures forming a mixed self-assembled mono-layer on Au(100) surfaces under ambient conditions. Finger-like ordered structures with a relative height of 0.10-0.20 nm, average width of 2.0 nm and variable lengths were observed using scanning tunneling microscopy under room temperature and ambient pressure conditions. Using X-ray photoemission spectroscopy, it was determined that L-cysteine molecules bind to the gold surface through the sulfur atom of their thiol group in two molecular configurations: neutral and zwitterionic. We found that the finger-like structures are the result of complex interactions of L-cysteine molecules with gold surfaces and L-cysteine molecules with methanol molecules and among all three components of the system (L-cysteine + methanol + gold surfaces). These interactions were detected through attenuated total reflectance-Fourier transform infrared spectroscopy. Furthermore, adsorbate/substrate interactions were studied by employing ab initio calculations using density functional theory, resulting in molecular arrangements formed by chains of L-cysteine pairs surrounded by physisorbed methanol molecules.

Remediation of water containing lead(II) using (3-iminodiacetic acid) propyltriethoxysilane graphene oxide

A novel chelating adsorbent based on (3-iminodiacetic acid) propyltriethoxysilane graphene oxide (IAT-GO) has been developed, showing exceptional promise for capturing lead. IAT-GO is made by combining a high-surface-area graphene oxide with a specially designed chelating ligand, which can selectively and efficiently remove lead. The synthesis of IAT-GO involves a two-step progression. In the first step, covalent bonds form between graphene oxide and (3-aminopropyl)-triethoxysilane (AT) through hydrolysis, condensation, and epoxide ring opening reactions. In the second step, nucleophilic substitution reactions occur between the primary amines and chloroacetic acid (CAA). A comprehensive suite of characterization techniques, including XPS, UV–Vis, XRD, Raman, FTIR, TEM, and SEM, provides detailed insights into the IAT-GO adsorbent's chemical composition and physical form, elucidating its intricate structure and morphology. Optimizing the experimental conditions for using the adsorbent material to remove Pb(II) ions from contaminated water revealed a maximum adsorption capacity of 124.0 mg/g at pH 5 and 30 min. The IAT-GO displays high selectivity for Pb(II) in a mixture of six metal ions containing 100 ppm of each one. Moreover, the IAT-GO shows 100% removal of Pb(II) for concentrations lower than 50 ppm. The excellent fit of the experimental data with the Langmuir adsorption isotherm and pseudo-second-order kinetic models (R2 > 99%) indicates that Pb(II) ion uptake onto the IAT-GO surface occurs via the monolayer formation of mercury ions. IAT-GO demonstrates exceptional potential as an innovative adsorbent for lead-contaminated water. Nitric acid (0.4 M) effectively regenerates the material, while its reusability remains impressive even after five cycles (> 97% removal efficiency). Therefore, this study highlights the development of a groundbreaking material, IAT-GO, with exceptional potential for remediating lead-contaminated water. Its high efficiency, selectivity, reusability, and cost-effectiveness make it a promising candidate for real-world applications.

(Invited) 2D Semiconductors from Spin-on Molecular Chemistries for Direct Large-Scale Integration

In this talk, I will discuss our recent developments centered on a process to produce fully soluble solutions from a unique molecular chemistry. This enables the creation of wafer-scale monolayers of MoS2, a prominent 2D semiconductor for logic and memory devices. This molecule can be dissolved in common solvents and spin-coated onto various substrates, including crystalline substrates, printed electrodes, and polymers. It can also be integrated into gate-all-around (GAA) 3D transistor structures for logic devices. Our method of rapidly synthesizing large-area MoS2 films, particularly in monolayer form via spin-coating, represents a novelty, as it hasn't been demonstrated previously with a single-source chemistry. This advancement is a significant step toward scalable synthesis of wafer-scale 2D semiconductor thin films, eliminating the need for post-growth wafer transfer techniques, a requirement with films grown by chemical vapor deposition (CVD) methods. Our fabrication process highlights the potential of using a single-source chemical precursor to develop monolayer 2D semiconductors that exhibit commendable transport characteristics and optical properties, which enhance with rising crystallization temperatures. Consequently, it holds promise as a semiconductor for microelectronic transistor channels in both back-end-of-line (BEOL) and front-end-of-line (FEOL) architectures.

Antimicrobial Peptide-Based Sensor for the Electrochemical Detection of Methicillin-Resistant Staphylococcus Aureus

Methicillin-resistant Staphylococcus aureus (MRSA) is a gram-positive bacterium that colonizes on the skin and nasal track of humans, which can lead to serious illnesses such as skin and soft tissue infections, pneumonia, and septicemia.MRSA is resistant to an entire class of antibiotics called beta-lactams, including penicillin, amoxicillin, and oxacillin, making it more difficult to treat. Culture based methods and molecular based methods like PCR are currently being used for the detection of MRSA, but these methods possess the drawbacks of being slow and expensive, respectively. Thus, we focused on developing a reagentless, cost-effective, near real-time detection method for intact MRSA cells.Antimicrobial peptides (AMPs) possess the ability to interact with bacterial cells by inhibiting their growth or by lysing them.However, this initial interaction between the cationic AMPs and the negatively charged bacterial cells can be used for the detection of pathogens like MRSA. Here, we used a MRSA-specific antimicrobial peptide, DP7, to fabricate an electrochemical peptide-based (E-PB) sensor. The DP7 probe was further modified with a methylene blue redox label and an alkanethiol chain which allows for the formation of a thiol-gold self-assembled monolayer. The sensor surface was passivated with both 6-mercapto-1-hexanol and a thiolated tetra-thymine sequence to prevent surface fouling. Electrochemical detection of MRSA was accomplished using alternating current voltammetry. Control experiments were performed using two gram-positive bacteria, Bacillus subtilis and Staphylococcus epidermidis, and two gram-negative bacteria, Escherichia coli and Pseudomonas aeruginosa. The DP7 sensor responded to MRSA in a concentration-dependent manner and was proven to be selective for MRSA over the other four microbes. Specifically, the % signal suppression obtained for MRSA was much larger when compared to those obtained for the other microbes. The same behavior was observed in pure buffer and 5% synthetic wound fluid. In addition, the detection time was relatively short, with signal saturation in less than 60 min. Overall, the DP7 sensor has demonstrated to possess attributes similar to other E-PB sensors. It has the potential to be developed as a rapid, reliable, and cost-effective diagnostic tool for MRSA, which will be useful in preventing the spread of the pathogen in the community. Furthermore, this sensing platform is versatile and can be redesigned for detection of other pathogenic bacteria.

Characterization and Adsorption Capacity Evaluation of ZnCl2 Impregnated Cassava Peel Carbon for Removal of Fe, Ca, Mg and Zn ions in Wastewater from Cassava processing Industry

The objective of this paper was to prepare, characterize and evaluate the adsorption capacity of cassava peel carbon (CPC) impregnation with ZnCl2 salt for the removal of Fe, Ca, Mg and Zn ions in wastewater derived from cassava processing which has been noted to be problematic in terms of management. CPC and cassava peel activated carbon (CPAC) at 1:3, 2:3, and 1:1 impregnation levels were placed in fixed bed adsorption columns to determine metal ion adsorption capacities of the carbon materials after 120, 240, 360 and 480-minute contact times. Langmuir and Freundlich isotherm models were used in assessment of adsorption of the carbon materials, while pseudo-first and second order models were used to validate the adsorption kinetics of Fe, Ca, Mg and Zn. Pore space development was also monitored using scanning electron microscope (SEM) imagery. Results SEM images revealed hexagonal honeycomb surface structure at 2:3 impregnation level and spongy configuration at 1:1 ZnCl2 impregnation level. The correlation coefficient of Langmuir isotherm was observed to be between 0.86 to 1, indicating that the adsorbent is very good in adsorption of the metals, however, Freundlich isotherm is found to be unfavorable in describing CPAC’s capacity in adsorbing zinc ion contaminant. The pH of the carbon materials was observed to have increased while the bulk density reduced with increasing level of impregnation. Conclusively, CPC and CPAC materials are well suited to Langmuir isotherm as well as pseudo-second order model, implying that adsorption occurs well in a monolayer form on the surface material surface.

Cationic homopolypeptides: A versatile tool to design multifunctional antimicrobial nanocoatings

Postoperative infections are the most common complications faced by surgeons after implant surgery. To address this issue, an emerging and promising approach is to develop antimicrobial coatings using antibiotic substitutes. We investigated the use of polycationic homopolypeptides in a layer-by-layer coating combined with hyaluronic acid (HA) to produce an effective antimicrobial shield. The three peptide-based polycations used to make the coatings, poly(l-arginine) (PAR), poly(l-lysine), and poly(l-ornithine), provided an efficient antibacterial barrier by a contact-killing mechanism against Gram-positive, Gram-negative, and antibiotic-resistant bacteria. Moreover, this activity was higher for homopolypeptides containing 30 amino-acid residues per polycation chain, emphasizing the impact of the polycation chain length and its mobility in the coatings to deploy its contact-killing antimicrobial properties. However, the PAR-containing coating emerged as the best candidate among the three selected polycations, as it promoted cell adhesion and epithelial monolayer formation. It also stimulated nitric oxide production in endothelial cells, thereby facilitating angiogenesis and subsequent tissue regeneration. More interestingly, bacteria did not develop a resistance to PAR and (PAR/HA) also inhibited the proliferation of eukaryotic pathogens, such as yeasts. Furthermore, in vivo investigations on a (PAR/HA)-coated hernia mesh implanted on a rabbit model confirmed that the coating had antibacterial properties without causing chronic inflammation. These impressive synergistic activities highlight the strong potential of PAR/HA coatings as a key tool in combating bacteria, including those resistant to conventional antibiotics and associated to medical devices.

Enhanced optical properties of MoSe2 grown by molecular beam epitaxy on hexagonal boron nitride

Transition metal dichalcogenides (TMDs) like MoSe2 exhibit remarkable optical properties such as intense photoluminescence (PL) in the monolayer form. To date, narrow-linewidth PL is only achieved in micrometer-sized exfoliated TMD flakes encapsulated in hexagonal boron nitride (hBN). In this work, we develop a growth strategy to prepare monolayer MoSe2 on hBN flakes by molecular beam epitaxy in the van der Waals regime. It constitutes the first step toward the development of large area single crystalline TMDs encapsulated in hBN for potential integration in electronic or optoelectronic devices. For this purpose, we define a two-step growth strategy to achieve monolayer-thick MoSe2 grains on hBN flakes. The high quality of MoSe2 allows us to detect very narrow PL linewidth down to 5.5 meV at 13 K, comparable to the one of encapsulated exfoliated MoSe2 flakes. Moreover, sizeable PL can be detected at room temperature as well as clear reflectivity signatures of A, B, and charged excitons.

Adsorption capability and regenerability of carbon slit micropores for CO2 capture

To date, the exceptional performance of microporous carbon in CO2 capture has been widely acknowledged as a crucial step towards achieving global zero carbon emissions. In this molecular simulation study, we employ grand canonical Monte Carlo simulation (GCMC) to shed light on the significant influence of micropores on CO2 adsorption capability and regenerability, emphasizing the need for a rigorous selection of the swing adsorption process based on pore size. Our findings corroborate numerous experimental and numerical studies that the ultramicropore (pore size < 7 Å) is the appropriate range for CO2 capture, as it facilitates the formation of a horizontal monolayer of CO2 molecules. Furthermore, we highlight the importance of designing porous carbon materials with a large pore volume at the optimal ultramicropore sizes (approximately 5.8-6.4 Å depending on adsorption and desorption conditions) for obtaining high CO2 capture capacity and effective adsorbent regeneration. For the first time, taking into account the operational parameters of practical swing adsorption processes, our simulation study provides valuable guidance for selecting the most appropriate technology tailored to each specific range of micropore size in porous carbon. For porous carbon materials with an abundant volume of ultramicropores, pressure swing adsorption (PSA) and pressure-temperature swing adsorption (PTSA), as conventional and hybrid swing adsorption processes respectively, are the most effective practices, achieving high CO2 working capacity and regenerability exceeding 80%.

Programmable Crowding and Tunable Phases in a Binary Mixture of Colloidal Particles under Light-Driven Thermal Convection.

We employ photothermally driven self-assembly of colloidal particles to design microscopic structures with programmable size and tunable order. The experimental system is based on a binary mixture of "plasmonic heater" gold nanoparticles and "assembly building block" microparticles. Photothermal heating of the gold nanoparticles under visible light causes a natural convection flow that efficiently assembles the microscale building block particles (diameter 1-10 μm) into a monolayer. We identify the onset of active Brownian motion of colloidal particles under this convective flow by varying the conditions of light intensity, gold nanoparticle concentration, and sample height. We realize a crowded assembly of microparticles around the center of illumination and show that the size of the particle crowd can be programmed using patterned light illumination. In a binary mixture of gold nanoparticles and polystyrene microparticles, we demonstrate the formation of rapid and large-scale crystalline monolayers, covering an area of 0.88 mm2 within 10 min. We find that the structural order of the assembly can be tuned by varying the surface charge of the nanoparticles and the size of the microparticles, giving rise to the formation of different phases-colloidal crystals, crowds, and gels. Using Monte Carlo simulations, we explain how the phases emerge from the interplay between hydrodynamic and electrostatic interactions, as well as the assembly kinetics. Our study demonstrates the promise of self-assembly with programmable shapes and structural order under nonequilibrium conditions using an accessible setup comprising only binary mixtures and LED light.

Pentaerythritol-DOPA (PE-DOPA): A tetra-catechol derivative for versatile hydrophilic nanocoatings

Pentaerythritol (PE) was modified with 3,4-dihydroxy-L-phenylalanine (L-DOPA) to produce a tetra(catecholamine) tetra-ester derivative (PE-DOPA). Subsequently, PE-DOPA was used to dip-coat glass, stainless steel (SS) and various plastics under alkaline conditions and formed a poly(PE-DOPA) surface coating ranging in thickness between 1.0–3.0 nm on glass and 9.0–12.0 nm on SS, as estimated by X-ray photoelectron spectroscopy (XPS). The as-coated poly(PE-DOPA) showed increased hydrophilicity compared to the bare substrate, as demonstrated by water contact angle (WCA) measurements, whilst subsequent thermal annealing of poly(PE-DOPA) coatings on glass and SS at 120 °C for 6 h reversed the as-coated hydrophilicity through an indole ring formation reaction. The molecular structure of the poly(PE-DOPA) coating was investigated by adsorption studies, suggesting monolayer formation on glass and multilayer on SS. Surface modification of plastic substrates (e.g. Nylon, polyester, polyolefines, PTFE) was also confirmed at the molecular level by XPS and at bulk properties level by WCA. PTFE was the only plastic substrate that didn’t show any altering of its bulk hydrophilicity. Lastly, the fabrication of multilayer structures where poly(PE-DOPA) was coated by bovine serum albumin (BSA) allowed for a first assessment of poly(PE-DOPA) affinity for BSA and the associated possibility of tailoring poly(PE-DOPA) response.

Enhanced Migration of Fuchs Corneal Endothelial Cells by Rho Kinase Inhibition: A Novel Ex Vivo Descemet's Stripping Only Model.

Descemet's Stripping Only (DSO) is a surgical technique that utilizes the peripheral corneal endothelial cell (CEnC) migration for wound closure. Ripasudil, a Rho-associated protein kinase (ROCK) inhibitor, has shown potential in DSO treatment; however, its mechanism in promoting CEnC migration remains unclear. We observed that ripasudil-treated immortalized normal and Fuchs endothelial corneal dystrophy (FECD) cells exhibited significantly enhanced migration and wound healing, particularly effective in FECD cells. Ripasudil upregulated mRNA expression of Snail Family Transcriptional Repressor (SNAI1/2) and Vimentin (VIM) while decreasing Cadherin (CDH1), indicating endothelial-to-mesenchymal transition (EMT) activation. Ripasudil activated Rac1, driving the actin-related protein complex (ARPC2) to the leading edge, facilitating enhanced migration. Ex vivo studies on cadaveric and FECD Descemet's membrane (DM) showed increased migration and proliferation of CEnCs after ripasudil treatment. An ex vivo DSO model demonstrated enhanced migration from the DM to the stroma with ripasudil. Coating small incision lenticule extraction (SMILE) tissues with an FNC coating mix and treating the cells in conjunction with ripasudil further improved migration and resulted in a monolayer formation, as detected by the ZO-1 junctional marker, thereby leading to the reduction in EMT. In conclusion, ripasudil effectively enhanced cellular migration, particularly in a novel ex vivo DSO model, when the stromal microenvironment was modulated. This suggests ripasudil as a promising adjuvant for DSO treatment, highlighting its potential clinical significance.

Sustainable removal of methylene blue dye from textile effluents by magnetized Tea waste and Peanut shells

Methylene blue finds numerous applications across various industries but its prolonged exposure to living organisms can result in significant health risks. In this study, the adsorption of magnetized Peanut shells and Tea waste for methylene blue dye removal has been reported. The biosorbents were synthesized by co-precipitation method and their suitability for methylene blue adsorption was confirmed through characterization techniques including Scanning Electron Microscope, Fourier Transfer Infrared Spectroscopy and X-Ray Diffraction analysis. After optimizing for pH (8.0), temperature (312 k), biosorbents dosage 25 mg/L with contact periods (35 min for Tea waste@Fe3O4 and 40 min for Peanut shells@Fe3O4), and initial methylene blue concentrations (5 ppm), the removal percentages of 95.88 % for Tea waste@Fe3O4 and 84.11 % for Peanut shells@Fe3O4 were achieved effectively. The equilibrium data for MB dye adsorption fitted well with the Langmuir model (R2 = 0.99) for Tea waste@Fe3O4 which indicated the formation of monolayer formation of adsorbate at the surface of adsorbent and the Freundlich model (R2 = 0.98) for Peanut shells@Fe3O4 confirmed the multilayers formation of MB dye at the material surface. Kinetic studies specified that both Tea waste@Fe3O4 (R2 = 0.99) and Peanut shells@Fe3O4 (R2 = 0.99) followed the pseudo-second order. Thermodynamic analysis showed that the adsorption process on Tea waste@Fe3O4 and Peanut shells@Fe3O4 was spontaneous (−ΔG) and endothermic. Tea waste@Fe3O4 exhibited ΔH (27.97 kJ/mol) and entropy ΔS (93.69 kJ/mol) while ΔH = 208.9 kJ/mol and ΔS 62 kJ/mol were found for Peanut shells@Fe3O4. The performance of the proposed biosorbent in industrial effluent demonstrated their effectiveness, highlighting their potential as a cost effective and sustainable solution for wastewater treatment.