Modification Agent Research Articles

Calcium nitrate as a modifier agent for metakaolin-based geopolymer mortar

Calcium nitrate, that is a calcium source, is generally used as an accelerating agent, antifreezing admixture, and corrosion inhibitor for Portland cement systems. Metakaolin, which is regularly used as a precursor in the production of geopolymers, lacks calcium. This can cause inefficiency of the geopolymerization process and alter the properties of the cementitious product. To overcome this problem, the potential benefits of adding calcium nitrate as an alternative calcium source for the metakaolin geopolymer mortar were investigated. Different ratios of calcium nitrate, ranging from 0.5 % to 10 %, were added into metakaolin geopolymer mortar. Different tests were conducted to know the effect of calcium nitrate on some properties of metakaolin geopolymer specimens, which were cured in either air or water. Advanced analysis methods were leveraged to unlock deeper meaning from the findings. The results indicated that adding calcium nitrate led to increased flowability and shortened setting time. The addition of 0.5–7 % calcium nitrate increased mechanical strength but reduced transport properties, whilst the addition of 10 % calcium nitrate led to adverse effects. The addition of 0.5–7 % calcium nitrate can mitigate the strength deterioration rate resulting from water curing and decrease drying shrinkage. The incorporation of appropriate ratios of calcium nitrate can form calcium silicate hydrate gel and densify the microstructure.

Improved composite network via bismuth iodide for efficient ice-nucleating application

The urgent demand for electricity requires more safe energy transportation. AgI-based weather modification agents are commonly employed to facilitate ice nucleation and remove the undesirable glaze icing to suppress the negative effects of natural disasters. However, the intrinsic nucleation potency of AgI strictly limits its further improvement. Here, a hexagonal BiI3 was added in AgI-based agents. The chemical interactions of BiI3 and precursors optimize the crystallization of the polymer composite, leading to an oriented composite network. In addition, BiI3 could alter the structure and morphology of the combustion products, therefore creating more possible heterogeneous nuclei sites. The resultant BiI3-modified AgI-based weather modification agent exhibits an ice nucleation ∼ 1014, which is nearly ten times higher than the sample without AgI-BiI3, leading to a 71.21 % enhancement of deicing efficiency compared to AgI sample. Our results indicate the effectiveness of BiI3 dopant to improve both nucleation and deicing performance for weather modification applications.

Salt-free neutral dyeing of cotton fiber with monochlorotriazine type reactive dyes

In this paper, we present the modification of cotton with glycidyltrimethylammonium chloride (GTA), demonstrating its capability not only for salt-free dye adsorption but also for achieving fixation reactions with monochlorotriazine-type reactive dyes under neutral conditions. The results of adsorption kinetics and isotherm experiments indicate that the adsorption of reactive dyes by modified cotton is chemisorption. Color-stripping experiments conducted on modified cotton dyed with different dyes revealed that GTA-modified cotton underwent fixation reactions with monochlorotriazine-type reactive dyes under neutral conditions. The reaction sites of modified cotton with reactive dyes were determined by measuring the 1H NMR of the model reaction products. Mechanism investigation using Density Functional Theory (DFT) on the fixation reaction revealed that the hydroxyl groups on the modification agent chain exhibit a lower pKa value and carry more negative charge, resulting in a lower reaction barrier with monochlorotriazine-type reactive dyes. Our research findings demonstrate that GTA-modified cotton fiber enhance the reactivity of cotton, providing significant guidance for the development of novel modifiers.

Matrix matters: How extracellular substances shape biofilm structure and mechanical properties

Biofilms possess unique mechanical properties that are vital to their stability and function. Biofilms are made of extracellular polymeric substances (EPS) secreted by microorganisms and comprise polysaccharides, proteins, extracellular DNA (eDNA), and lipids. EPS is the primary contributor and driver of the biofilm structure and mechanical properties such as stiffness, cohesion, and adhesion. EPS enhances the elasticity and viscosity of biofilms, allowing them to withstand mechanical stresses, shear forces, and deformation. Therefore, biofilms are notoriously difficult to remove and can result in billions of dollars in losses for various industries due to their adverse effects, such as contamination, pressure loss, and corrosion. As a result, it is essential to comprehend the mechanical properties of biofilms to control or remove them in various scenarios. We undertook a fundamental study to determine the relationship between individual EPS components and biofilm mechanical properties. In this study, a CDC biofilm reactor was used to grow pure culture biofilms (Staphylococcus epidermidis) which were treated with six EPS modifier agents (Ca2+, Mg2+, periodic acid, protease K, lipase, and DNAase I) to modify or cleave specific EPS components. The mechanical properties (Young's Modulus) of treated biofilms were subsequently tested using atomic force microscopy (AFM), the biofilm EPS functional groups were measured via the Fourier transform infrared (FTIR) spectroscopy, and biofilm structural characteristics using confocal imaging. The FTIR results showed that EPS modifier agents successfully reduced their target EPS components. Similarly, the confocal microscopic analysis results showed that most of these modifier agents (except lipase) significantly reduced (P-value <0.05) the biovolume and thickness of treated biofilms. Conversely, most of these modifier agents (except protease K) significantly increased (P-value <0.05) the roughness coefficient of the biofilms. Finally, data from AFM showed that biofilm mechanical properties (Young’s modulus) significantly (P-value <0.05) changed with their EPS composition. These results have significant ramifications for biofilm management and control in myriad scenarios.

Highly Stable Oil-Soluble Iron-Sulfur Nanoparticles: Preparation, Characterization and Electrochemical Properties

To improve the stability of iron-sulfur clusters to air, an oil-soluble dialkyidithiophosphate (DDP) as a modifier, stabilizer, and coordination agent, was used to prepare highly stable iron-sulfur NPs in water-alcohol mixed solvents in this work. The morphology, surface composition, microstructure, stability and electrochemical properties of the as-prepared iron sulfure NPs were characterized by many techniques, such as Uv-vis, FT-IR, TEM, Raman, TG, and electrochemical analyzer. The results showed that DDP had been successfully covalently bonded onto iron sulfur NPs surface, and endowed the iron sulfur NPs with excellent oil-solubility, high stability, and good electrochemical performance. The stability test showed that the powders of iron sulfur NPs had excellent stability when exposed to oxygen. The electrochemical tests indicated that the iron sulfur NPs had excellent electrochemical reversibility. These findings suggest that the iron sulfur NPs prepared in this work has similar structure and electrochemical reversibility as the iron-slufur clusters in living organisms, and lays the foundation for its application in microelectronic devices and sensors.

Epigenetic changes driven by environmental pollutants in lung carcinogenesis: a comprehensive review.

Lung cancer remains the leading cause of cancer-related mortality globally, with environmental pollutants identified as significant risk factors, especially for nonsmokers. The intersection of these pollutants with epigenetic mechanisms has emerged as a critical area of interest for understanding the etiology and progression of lung cancer. Epigenetic changes, including DNA methylation, histone modifications, and non-coding RNAs, can induce alterations in gene expression without affecting the DNA sequence and are influenced by environmental factors, contributing to the transformation of normal cells into malignant cells. This review assessed the literature on the influence of environmental pollutants on lung cancer epigenetics. A comprehensive search across databases such as PubMed, Web of Science, Cochrane Library, and Embase yielded 3,254 publications, with 22 high-quality papers included for in-depth analysis. These studies demonstrated the role of epigenetic markers, such as DNA methylation patterns of genes like F2RL3 and AHRR and alterations in the miRNA expression profiles, as potential biomarkers for lung cancer diagnosis and treatment. The review highlights the need to expand research beyond homogenous adult male groups typically found in high-risk occupational environments to broader population demographics. Such diversification can reduce biases and enhance the relevance of findings to various clinical contexts, fostering the development of personalized preventive and therapeutic measures. In conclusion, our findings underscore the potential of innovative epigenetic therapies, such as DNA demethylating drugs and histone modification agents, to counter environmental toxins' carcinogenic effects. The growing interest in miRNA therapies and studies aiming to correct aberrant methylation patterns indicate significant strides toward better lung cancer management and a healthier future for global communities.

Silica surface modification using cellulose as a renewable organosilane derived from coconut coir fiber for carbon capture

The properties of silica surface modification for carbon capture were studied, utilizing cellulose-amine as a modification agent derived from dissolved coconut coir fiber. To form bonds with NH2 functional groups through amination processes, cellulosic biomass waste is utilized, which is analogous to replacing alkoxy ligands. The dual-function mixture reagents dimethyl sulfoxide (DMSO) and ammonium hydroxide (NH4OH) were employed in the same system as the amine sources and solvents. Waterglass is used as a source of silica, and the modified particles are formed using a one-step consecutive sol-gel spray drying process used in a direct condensation route. Changes in the concentration of sodium lauryl sulfate (SLS) were examined to determine how they affected the essential parameters of the particles. The template is removed during particle formation without further physical or chemical processing. The particle morphology changed from donut-shaped to spherical after SLS application, as evidenced by the increase in SLS concentration. This also shows that the increase in the particle surface area is directly influenced by the increase in the formation of new pore structures with increasing SLS concentration. Through this mechanism, it is possible to extend the pore size distribution to the meso-macropore regime and initiate the formation of new mesopores. This has a direct impact on the capacity to absorb CO2 gas by increasing the cellulose-amine mass fraction that can be grafted to as high as 32.35 %wt. At an operating pressure of 6 bar, a maximum CO2 gas adsorption capacity of 5.32 mmol/g silica was attained by adding SLS 3 CMC to the silica particles. This value is 2.3 times higher than that obtained when using an aminosilane-based modification agent.

Microencapsulated phase change material in 3D-printable mortars

The present study investigates the potential of replacing sand with microencapsulated phase change materials (MEPCM) in 3D-printable mortar to provide a promising way to improve thermal performance in 3D-printed buildings. Adding MEPCM significantly enhanced the rheological properties and early hardening evolution of cementitious mortar for 3D printing applications without the need for viscosity modifier agents. In hardened mortars, microstructural analysis and thermal cycling experiments confirmed that MEPCM remained intact and stable within the cementitious environment. The thermal properties of the treated mortars, including latent heat and thermal conductivity, were improved for energy-saving applications. Despite this, the compressive strength of the mortars dropped considerably by increasing the concentration of MEPCM while a strength of above 20 MPa was maintained. Simulation results from 3D Finite Element Method (FEM) and 1D reduced order model (ROM) closely matched the experimental data from printed walls in a thermal setup, validating the use of 1D ROM simulations for long-term predictions. In a case study, a printed wall where MEPCM replaced 80 % of the sand showed a ∼40 % reduction in energy consumption compared to mortar without MEPCM under real weather conditions.

Oral cyclophosphamide treatment for clinical periocular inflammation of unknown origin

Abstract: This study outlines a scenario involving unilateral periocular inflammation exhibited resistance to conventional immunomodulatory therapy (IMT) and biologic response modifying agents, which was successfully managed with oral cyclophosphamide monotherapy. A 39-year-old male visited our clinic, expressing discomfort and swelling in his left upper eyelid for six months. All multidisciplinary consultations and imaging yielded normal results. He remained consistently on a dosage of 50 mg oral prednisone. Blood tests yielded results within the normal range or were negative, with the exception of the antinuclear antibody. He did not respond to conventional IMT and biological response modifier agents. Ultimately, the patient began oral cyclophosphamide. One month after commencing cyclophosphamide treatment, the oral prednisone dosage was gradually reduced without any flare-up. oral cyclophosphamide can serve as a valuable treatment for periocular inflammation that does not respond to standard conventional IMT and biologic response modifier agents.

Sustainable Approaches for the Fabrication of Nanocellulose-Polyamide Membrane Based on Waste Date Palm Leaves for Water Treatment

A vast amount of agricultural waste, such as dried leaves, stems, pits, seeds, etc., are produced by date palm trees in Saudi Arabia each year. This waste is an excellent source of degradable biomass suitable for many uses. Crystalline nanocellulose (CNC) is one of the most important nanomaterials that can be used in various applications. Due to its unique properties, which include biorenewability, optical transparency, high mechanical strengths, and sustainability, nanocrystalline cellulose has become a significant nanomaterial in recent years. In this study, CNC was isolated from the waste date palm leaves and used for the production of PA-modified membranes for water treatment by reverse osmosis membrane technology. The membranes were prepared by surface polymerization with the polyamide as a selective layer on the polysulfone support film. Three membranes were produced, two with 0.01% and 0.02% (w/v) CNC and the third with PA-free CNC for comparison. Each membrane produced was tested using different characterization techniques. The polyamide membrane with 0.01% w/v CNC had a higher water permeability of 43.25 L/m2 h bar than the membranes with 0% w/v CNC (36.25 L/m2 h) and 0.02% w/v CNC (42.85 L/m2 h bar). Under the same conditions, salt retention was also found to be above 98% for both NaCl and MgSO4 for the two modified membranes. The contact angle was found to be 68.04±3.7, 72.83±0.8, and 63.76±5.5 for PA(0%CNC), PA-CNC (0.01% w/v), and PA-CNC (0.02% w/v), respectively. The 0.01% PA-CNC membrane exhibited a higher water contact angle, greater hydrophobicity and lower surface roughness. As a result, the isolated CNC might be appropriate for use as a modifier agent for membrane fabrication and water treatment.

Removal of quinoline in aqueous solutions using chemically modified and unmodified hydrochars from lotus seedpods: A comprehensive experimental study

In this study, a novel hydrochar adsorbent derived from lotus seedpods was synthesized and subsequently modified to enhance its adsorption efficiency for quinoline contaminated wastewater. Using lotus seedpods as biomass raw material, lotus seedpod hydrochar (LSH) was prepared by hydrothermal carbonization method, and it was modified with hydrochloric acid (HA) and phosphoric acid (PA) as modifiers to improve adsorption efficiency. The adsorption kinetics and isotherms of quinoline on both the unmodified and modified hydrochars were studied in detail to elucidate the underlying adsorption mechanisms. Furthermore, the effect of coexisting organic pollutants, i.e. phenol and pyridine, commonly found in coking effluents, on the quinoline adsorption efficiency of hydrochar was investigated. The regenerative potential of the adsorbent was explored through desorption studies to assess the reusability and practicality of hydrochar post-adsorption. The optimal conditions for modified LSH were determined as follows: an adsorbent dosage of 3 g/L, pH of 3, an initial quinoline concentration of 200 mg/L, and a contact time of 90 minutes. The maximum adsorption capacities for PA-LSH and HA-LSH were 48.59 mg/g and 49.12 mg/g, respectively. Among the types of modification agents, acid modifiers, particularly 20 % phosphoric acid and 20 % hydrochloric acid, significantly enhanced the adsorption efficiency, increasing the adsorption rates by 24.24 % and 14.56 %, respectively, compared to unmodified hydrochar (64.06 %). Coexisting pollutants minimally affected quinoline adsorption, with phosphoric acid-modified hydrochar maintaining 80.33 % removal in simulated coking wastewater. Regeneration with hydrochloric acid showed improved utility, with modified hydrochar sustaining over 80 % adsorption after three cycles. This research not only presents an innovative approach to the development of efficient adsorbents for quinoline removal, but also provides insight into the adsorption behavior of hydrochar in the complex wastewater systems. The findings contribute to both the advancement of sustainable water treatment technologies and the use of biomass-derived materials for environmental remediation. As such, this work holds promise for applications in wastewater treatment and environmental remediation.

Nanographene Oxide Promotes Angiogenesis by Regulating Osteoclast Differentiation and Platelet-Derived Growth Factor Secretion.

An imbalanced system of angiogenesis-osteoblasts-osteoclasts is regarded as the main factor in bone remodeling dysfunction diseases or osseointegration loss. Osteoclast precursors are the key cells that accelerate bone-specific angiogenesis and maintain normal osteoblast and osteoclast function. Graphene oxide is an effective scaffold surface modification agent with broad application prospects in bone tissue engineering. However, the effect of graphene oxide on the interaction between osteoclasts and angiogenesis has not yet been elucidated. In this study, a rat calvarial defect model was established and treated with an electrochemically derived nanographene oxide (ENGO) hydrogel. Higher angiogenesis and platelet-derived growth factor (PDGF) B in preosteoclasts were observed in the ENGO group compared with that in the control group. Moreover, in vitro experiments demonstrate the efficacy of ENGO in substantially reducing the expression of the receptor activator of nuclear factor-kappaB ligand (RANKL)-induced osteoclast-associated markers and inhibiting bone resorption activity. Additionally, ENGO enhances the secretion of the osteoclast-derived coupling factor PDGF-BB and promotes angiogenesis. Our investigation revealed the crucial role of isocitrate dehydrogenase 1 (IDH1) in the ENGO-mediated regulation of osteoclast differentiation and PDGF-BB secretion. The decreased expression of IDH1 reduces the level of histone lysine demethylase 7A (KDM7A) and subsequently increases the H3K9me2 level in the cathepsin K promoter region. In summary, we found that ENGO promotes angiogenesis by inhibiting the maturity of RANKL-induced osteoclasts and enhancing PDGF-BB secretion. These results indicate that ENGO holds promise for the application in fostering osteoclast-endothelial cell crosstalk, providing an effective strategy for treating bone resorption and osteoclast-related bone loss diseases.

Interfacial engineering and defect passivation of SnO2 through agmatine sulfate in carbon-based perovskite solar cells

Electron transport layer has always played a crucial role in the performance of the perovskite solar cells (PSCs). Particularly, SnO2-based PSC has sparked considerable interest due to its superior properties. Even with such remarkable properties, certain challenges persist such as agglomeration of SnO2 particles which can lead to interfacial defects and poor morphology. To solve this problem, Agmatine Sulfate (AGTS) has been introduced as an interfacial modification agent which with the help of its active functional group including amide (-NH2) and hydroxyl (OH) has allowed to facilitate the interaction at the interface between SnO2 and perovskite. The interaction facilitates the growth of perovskite crystals while tuning the energy levels which has boosted the charge transfer capability of the layer. All these improvements in the properties have led to enhanced power conversion efficiency (PCE) from 11.17 % to 15.20 % for the encapsulated device. Furthermore, the modification also improved the long-term stability of the device as the AGTS-modified devices retained 87 % of their performance at 15–25 °C with humidity levels between 10 and 20 % for over a period of 31 days. Finally, the devices prepared with the AGTS also showed repeatability in their performance while boosting the overall performance of carbon-based PSCs (C–PSCs) and indicating a novel approach to not only increase but also accelerate the commercialization of C-PSC.

Engineered Immunomodulatory Nanoparticles Inhibit Root Resorption and Ankylosis

IntroductionExternal root resorption following avulsion injury is a complex process wherein differentiation of macrophages (Mϕ) to multinucleated osteoclasts is temporally regulated by resident periodontal fibroblasts (PDLF). The current study aims to assess the effect of engineered bioactive chitosan nanoparticles (CSNP), sustained released dexamethasone conjugated CSNP (CS-DEX) and CSNP functionalized with photosensitizer Rose Bengal (CSRB) for application in root resorption using an in-vitro PDLF-Mϕ direct coculture model and in-vivo delayed reimplantation model. MethodsPDLF-Mϕ direct coculture system was exposed to lipopolysaccharide (LPS), macrophage colony stimulating factor, receptor activator of nuclear factor kappa β ligand with or without CSNP/CS-DEX for 7 days. Clastic differentiation was assessed by tartrate resistant acid phosphatase (TRAP) staining on day 7. On day 2 and 7, immunofluorescence analysis was conducted to assess the expression of Mϕ polarization markers (CD80, CD206), multinucleation markers (NFATc1, STAT6) in Mϕ and matricellular protein periostin in PDLF and cytokine profiling in cell culture supernatants. Delayed replantation model with extraoral air dry/LPS exposure for 1h followed by root surface treatment with CS-DEX/CSRB was used in Wistar rats. After 21 days, rats were euthanized for histologic and immunofluorescence analysis. Statistical analysis one-way ANOVA with Tukey's multiple comparisons was used to analyze the data (P < .05). ResultsCS-DEX significantly reduced TRAP+ multinucleated cells and CSNP treatment showed no TRAP+ cells. Immunofluorescence analysis showed that CSNP/CS-DEX reduced CD80, NFATc1 and STAT6 expression and increased periostin as expressed by fluorescence intensity. CSNP/CS-DEX significantly reduced TNFα, MMP9 and increased IL10, TGFβ1. Osteoprotegerin was upregulated only by CSNP. Root surface treatment in delayed replantation model showed that CS-DEX and CSRB substantially reduced the degree of resorption and ankylosis. Further, CD80, CD206, and MMP2 expression in groups with root surface treatment with CS-DEX and CSRB was lower than airdry/LPS group and similar to healthy control and NFATc1, STAT6, and MMP9 expressions were lower than healthy control. ConclusionThe engineered nanosized immunomodulatory bioactive materials chitosan nanoparticles functionalized with photosensitizer and dexamethasone effectively reduced the clastic differentiation of Mϕ in in-vitro coculture and minimized the resorption and ankylosis in a delayed reimplantation model. These biomaterials have the potential to serve as root modification agents, promoting favorable healing outcomes in cases of dental avulsion.

Green adsorption of quinoline as basic N-compounds from liquid fuel using mesoporous and Fe-functionalized walnut shell-activated carbon

Removing nitrogenous compounds from liquid fuels is essential, and adsorption de-nitrogenation is a new process for this goal. This work has the purpose of investigating quinoline adsorption using Iron functionalized Activated carbon (IFAC) mesoporous nanocomposite. The mesoporous nanocomposite was synthesized in a one-step process by chemical activation of the walnut shell using Iron chloride as the activation and modification agent. The IFAC mesoporous nanocomposite was utilized to remove quinoline from isooctane as the liquid fuel via a discontinuous (batch) process by examining the effect of initial concentration, contact time, and temperature. The effect of contact time on the adsorption ability of IFAC for quinoline was well described by the pseudo-second-order model. The Langmuir model described the equilibrium manner of the process well, and the adsorbent could retain 344.82 mg/g of quinoline (37.37 mg N/g). The thermodynamic parameters show the endothermic (ΔH°= +30.070 kJ/mol) and spontaneity of the adsorption process. The regeneration experiments indicated that functionalized AC’s adsorption ability for quinoline adsorption decreased by 23% after five cycles. The obtained data indicate that the functionalization of activated carbon surface with iron particles leads to improving its adsorption ability toward N-containing compounds from liquid fuels.

Lithium-Ion battery silicon Anodes: Surface engineering with novel additives for enhanced ion and electron transport

Silicon (Si) stands as a promising candidate for high-capacity anode materials in the next-generation lithium-ion batteries (LIBs) due to extremely high specific capacity. However, silicon application is hindered by its inherently poor electron and ion conductivities, as well as structural instability during the repeated charging/discharging. To address these challenges, a novel functional surface modification agent, diethylenetriaminepenta(methylenephosphonic) acid (DTPMP), was decorated on the surface of silicon particles for the first time. The experimental results demonstrate that the DTPMP effectively enhances the cohesion between nano Si particles. This study combines experimental observations with theoretical calculations to analyze the nucleophilic and electrophilic sites of DTPMP and carboxymethyl cellulose (CMC), elucidating the existence state of DTPMP on the nano Si surface. Furthermore, by examining the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO), along with the electrostatic potential (ESP) of DTPMP and solvent molecules in conjunction with Li+, the impact of the phosphate group on the diffusion of Li+ and electrons at the nano Si surface was studied. The electron density difference (EDD) maps for DTPMP and CMC reveal that DTPMP exhibits a more pronounced response in the presence of an electric field, suggesting its enhanced role in facilitating Li+ diffusion. This research offers a novel perspective on enhancing the electrochemical performance of nano Si surfaces, paving the way for the development of advanced LIBs with improved energy storage capabilities.

Wool fiber as an In situ reducing agent towards ZnO-based surface modified fabric development: Durability assessment in the realm of textile applications

The development of a bio-inspired method to fabricate ZnO nanostructure-modified functional wool fabric represents a substantial challenge in the textile field. This article reports for the first time the use of wool as a reducing agent for the synthesis of ZnO nanoparticles. While previous studies have employed alternative natural reducing agents for surface modification of host materials, this investigation uniquely utilizes the host material, wool, as the reducing agent for in-situ ZnO nanoparticle synthesis. In addition to demonstrating the use of wool as a reducing agent, this literature uniquely reports the durability of the modified fabric, achieved through the use of trimethoxy methyl silane. This silane compound acts as a bridging agent, forming a strong interface between the wool fibers and the synthesized ZnO nanoparticles. This innovative approach enhances the adhesion and stability of the ZnO nanoparticles on the wool fabric, a key aspect that contributes to the overall durability and performance of the modified material. The in situ surface modification process employed a metal oxide precursor (zinc acetate dihydrate), capping agents (hexamethylene tetraamine, sodium carbonate, and sodium sulfate), and a coupling agent (trimethyl methoxy silane). The capping agents were used to control the reaction conditions, while the coupling agent was employed to improve the durability of the surface modification. The impact of three different capping agents on the corresponding synthesis process was assessed, and the findings revealed that the choice of capping agent helped to form ZnO nanoparticles with distinct morphologies. Analytical techniques, such as X-ray diffraction (XRD), scanning electron microscopy (SEM), dynamic light scattering (DLS), and attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy, were utilized to characterize the synthesized particles and the treated fabric. The XRD analysis coupled with SEM analysis confirmed the successful formation of ZnO nanoparticles. The ATR-FTIR spectroscopy provided evidence of the formation of Si-O-Zn and Si-O-C bonds, observed at around 920 cm−1 and 1040 cm−1 respectively. These spectroscopic findings indicate that the surface modification involving the silane compound has enhanced the durability of the ZnO-modified fabric. The covalent linkages between the ZnO nanoparticles, the silane compound, and the wool fibers, confirmed by SEM analysis before and after washing cycles, have enabled the durable attachment of the nanoparticles to the fabric surface, even after multiple washing cycles. The results suggest a novel pathway to use wool as a reducing agent for the surface modification of the same material. Detailed mechanistic insights into the surface modification process and the corresponding chemical interactions were also discussed.

Boron adsorption studies of poly(styrene-glycidyl methacrylate) latex: effect of modification agents

Poly(styrene-glycidyl methacrylate) (PSGMA) latex was synthesized by emulsion polymerization method. PSGMA latex was modified with N-methyl-d-glucamine (NMDG), 1,2-bis(3-aminopropylamino)ethane (BAPE), N-(2-hydroxyethyl)ethylenediamine (HEA), and N,N'-dimethylethylenediamine (NMEA). The presence of N amount varying between 2.1 and 4.4% in the results of elemental analysis showed that the modification was successful. Boron adsorption studies were carried out using these modified latexes. The study was carried out using the curcumin method by UV–vis spectrophotometry. For the most effective adsorption process, at pH value of 9, the boron concentration was 10 ppm and the contact time was 60 min. It was found that latex modified with NMDG had a higher adsorption capacity (0.195 mmol/g) than other modified latexes. Particle sizes were determined by dynamic light scattering spectrometry and scanning electron microscopy (SEM) analyses. The particle diameter of PSGMA latex was found to be approximately 140 nm in SEM analysis and the particles were almost monodisperse. After PSGMA latex was modified with NMDG, BAPE, HEA, and NMEA agents and boron adsorption was performed, it was observed that the particle diameters increased to approximately 170, 270, 220, and 260 nm, respectively. An elemental analyzer was used to determine the %N of the structures. The %B2O3 of the structures was determined with a thermogravimetric analyzer. While thermal analysis studies showed that organic components were completely removed from the structure at 700 °C, residues ranging from 4.8 to 10.4% (%B2O3) were found in boron adsorption polymers. The %B amounts were determined with an inductively coupled plasma mass spectroscopy device. It was observed that the amount of adsorbed boron varied between 0.42 and 0.95%, and the highest amount of %B belonged to latex modified with NMDG due to its very simple structure and the location of the –OH groups.Graphical

Enhancement of adsorption of cyanobacteria, Microcystisa aeruginosaby bacterial-based compounds

In the present study, algicidal bacteria cultivated in an aqueous medium were utilized as a surface modification agent to develop an efficient adsorbent for the removal of Microcystis aeruginosa. The modification considerably enhanced M. aeruginosa cell removal efficiency. Moreover, the introduction of bio-compounds ensured specificity in the removal of M. aeruginosa. Additionally, the cyanotoxin release and acute toxicity tests demonstrated that the adsorption process using the developed adsorbent is environmentally safe. Furthermore, the practical feasibility of the adsorptive removal of M. aeruginosa was confirmed through cell removal tests performed using the developed adsorbent in a scaled-up reactor (50 L and 10 tons). In these tests, the effects of the adsorbent application type, water temperature, and initial cell concentration on the M. aeruginosa removal efficiency were evaluated. The results of this study provide novel insights into the valorization strategy of biological algicides repurposed as adsorbents, and provide practical operational data for effective M. aeruginosa removal in scaled-up conditions.

Tin Oxide/Amphiphilic Polymer Double‐Layered Hole Transporter for High‐Efficiency Tin Perovskite Solar Modules

AbstractAn exquisite, engineering of two poor hole transporting materials (HTMs, SnO, and PDTON) to form an excellent double‐layered HTL (SnO/PDTON) for inverted tin‐perovskite solar modules (TPSMs) is developed. SnO/PDTON has better photovoltaic performance than the commonly used PEDOT:PSS HTM when large‐area TPSMs are fabricated. Thermally evaporated SnO (that is a simple, available oxide with high hole mobility, good transparency, and adjustable frontier orbitals energy levels) film is used as a main hole transporting layer (HTL). Amphiphilic polymer PDTON (having the amine and ether groups on the side chains) film is used as a Co‐HTL, cross‐linker, passivator, and interface modification agent, as unveiled various physicochemical studies. Double‐layered SnO/PDTON with a flat morphology and good affinity toward perovskite precursor solution creates also a proper surface for depositing large‐area, high‐quality TPsk film. Therefore, TPSM (25.2 cm2 active area on 10 cm × 10 cm ITO substrate) based on double‐layered SnO/PDTON HTL achieving an efficiency over 10% with a negligible current hysteresis is reported for the first time. This study emphasizes not only the exquisite design of combining the specific characteristics of two prosaic HTMs to become a good double‐layered HTL but also gives a direction toward fabricating TPSMs to be applied in all‐perovskite tandem solar module.