Search Results (233)

This study investigates the synergistic modification of cement–soil using waste brick powder (WBP) and polyvinyl alcohol (PVA) fibers to address the growing demand for sustainable construction materials and recycling of demolition waste. An orthogonal experimental design was employed with 5% WBP (by mass) and PVA fiber content (0–1%), evaluating mechanical properties based on unconfined compressive strength (UCS) and splitting tensile strength (STS) and microstructure via scanning electron microscopy (SEM) across 3–28 days of curing. The results demonstrate that 0.75% PVA optimizes performance, enhancing UCS by 28.3% (6.87 MPa) and STS by 34.6% (0.93 MPa) at 28 days compared to unmodified cement–soil. SEM analysis revealed that PVA fibers bridged microcracks, suppressing propagation, while WBP triggered pozzolanic reactions to densify the matrix. This dual mechanism concurrently improves mechanical durability and valorizes construction waste, offering a pathway to reduce reliance on virgin materials. This study establishes empirically validated mix ratios for eco-efficient cement–soil composites, advancing scalable solutions for low-carbon geotechnical applications. By aligning material innovation with circular economy principles, this work directly supports global de-carbonization targets in the construction sector. Full article

To address the growing demand for environmentally friendly flexible sensors, here, a composite hydrogel of nanocellulose (NC) and polyvinyl alcohol (PVA) was designed and fabricated using Camellia oleifera shells as a sustainable alternative to petroleum-based raw materials. Firstly, NC was extracted from Camellia oleifera shells and modified with 2-chloropropyl chloride to obtain a nanocellulose-based initiator (Init-NC) for atomic transfer radical polymerization (ATRP). Subsequently, sulfonyl betaine methacrylate (SBMA) was polymerized by Init-NC initiating to yield zwitterion-functionalized nanocellulose (NC-PSBMA). Finally, the NC-PSBMA/PVA hydrogel was fabricated by blending NC-PSBMA with PVA. A Fourier transform infrared spectrometer (FT-IR), proton nuclear magnetic resonance spectrometer (¹H-NMR), X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), universal mechanical testing machine, and digital source-meter were used to characterize the chemical structure, surface microstructure, and sensing performance. The results indicated that: (1) FT-IR and ¹H NMR confirmed the successful synthesis of NC-PSBMA; (2) SEM, TEM, and alternating current (AC) impedance spectroscopy verified that the NC-PSBMA/PVA hydrogel exhibits a uniform porous structure (pore diameter was 1.1737 μm), resulting in significantly better porosity (15.75%) and ionic conductivity (2.652 S·m⁻¹) compared to the pure PVA hydrogel; and (3) mechanical testing combined with source meter testing showed that the tensile strength of the composite hydrogel increased by 6.4 times compared to the pure PVA hydrogel; meanwhile, it showed a high sensitivity (GF = 1.40, strain range 0–5%; GF = 1.67, strain range 5–20%) and rapid response time (<0.05 s). This study presents a novel approach to developing bio-based, flexible sensing materials. Full article

We investigated the practical adhesion of a conventional poly(vinyl alcohol) glue with a glassy isosorbide-based polycarbonate (ISB-PC) comprising isosorbide and 1,4-cyclohexanedimethanol. The addition of 1 wt.% of a copolymer of vinyl alcohol and butenediol to the ISB-PC greatly improved its lap-shear strength. This improvement may be attributed to the dissolution of the copolymer chains in the ISB-PC, which had a low water droplet contact angle. Furthermore, the blend was transparent because most of the copolymer chains dissolved in the ISB-PC. Microplastics present a serious environmental issue, even for adhesives. Therefore, the present technique to modify ISB-PC to show good lap-shear strength with a biodegradable glue is attractive. Full article

Background/Objectives: Effective drug delivery systems require precise formulation and understanding of excipient impact on active pharmaceutical ingredient (API) stability and efficacy, as uncontrolled interactions can compromise outcomes. This study developed and validated a semi-solid extrusion (SSE) 3D printing method for polyvinyl alcohol (PVA)-based hydrogel disks with metronidazole (MET). These disks served as a standardized platform to assess excipient influence on MET’s antimicrobial activity, focusing on plasticizers (polyethylene glycol 400, glycerol, propylene glycol, and diethylene glycol monoethyl ether)—excipients that modify hydrogel properties for their application in printing dressing matrices—with the platform’s capabilities demonstrated using in vitro antimicrobial susceptibility testing against Bacteroides fragilis. Methods: Hydrogel inks based on PVA with added plasticizers and MET were prepared. These inks were used to 3D-print standardized disks. The MET content in the disks was precisely determined. The antimicrobial activity of all formulation variants was evaluated using the disk diffusion method against B. fragilis. Results: The incorporated plasticizers did not negatively affect the antimicrobial efficacy of MET against B. fragilis. All printed hydrogel matrices exhibited clear antimicrobial activity. The 3D-printed disks showed high repeatability and precision regarding MET content. Conclusions: SSE 3D printing is viable for manufacturing precise, reproducible MET-loaded PVA hydrogel disks. It provides a standardized platform to evaluate diverse excipient impacts, like plasticizers, on API antimicrobial performance. The tested plasticizers were compatible with MET. This platform aids rational formulation design and screening for optimal excipients in designed formulations and for various pharmaceutical applications. Full article

In this study, polyvinyl alcohol (PVA) films were reinforced with lignocellulosic nanofibers (LCNFs) extracted from bamboo shoot shells using a choline chloride-based deep eutectic solvent (DES). A filler loading of 10 wt% was identified as the optimal condition for enhancing film performance. To improve interfacial compatibility between the PVA matrix and LCNFs, three surface modification treatments were applied to the nanofibers: hydrochloric acid (HCl) hydrolysis, citric acid (CA) crosslinking, and a dual modification combining both methods (HCl&CA). Among all formulations, films incorporating dual-modified LCNF at 10 wt% loading exhibited the most significant improvements. Compared to neat PVA, these composites showed a 79.2% increase in tensile strength, a 15.1% increase in elongation at break, and a 33.1% enhancement in Young’s modulus. Additionally, thermal stability and barrier properties were improved, while water swelling and solubility were reduced. Specifically, the modified films achieved a thermal residue of 9.21% and the lowest degradation rate of 10.81%/min. Water vapor transmission rate and oxygen permeability decreased by 18.8% and 18.6%, respectively, and swelling and solubility dropped to 14.26% and 3.21%. These results highlight the synergistic effect of HCl hydrolysis and CA crosslinking in promoting uniform filler dispersion and strong interfacial adhesion, offering an effective approach to valorizing bamboo shoot shell waste into high-performance, eco-friendly packaging materials. Full article

This study focuses on the nameplate of Vila D. Bosco, a modern building in Macau from the time of Portuguese rule, and looks at the types of metal materials and surface coatings used, as well as how they corrode due to the tropical marine climate affecting the building’s metal parts. The study uses different techniques, such as X-ray fluorescence spectroscopy (XRF), scanning electron microscopy/energy dispersive spectroscopy (SEM-EDS), X-ray diffraction (XRD), attenuated total internal reflectance Fourier transform infrared spectroscopy (ATR-FTIR), and cross-sectional microscopic analysis, to carefully look at the metal, corrosion products, and coating of the nameplate. The results show that (1) the nameplate matrix is a resulfurized steel with a high sulfur content (Fe up to 97.3% and S up to 1.98%), and the sulfur element is evenly distributed inside, which is one of the internal factors that induce corrosion. (2) Rust is composed of polycrystalline iron oxides such as goethite (α-FeOOH), hematite (α-Fe₂O₃), and magnetite (Fe₃O₄) and has typical characteristics of atmospheric oxidation. (3) The white and yellow-green coatings on the nameplate are oil-modified alkyd resin paints, and the color pigments are TiO₂, PbCrO₄, etc. The surface layer of the letters is protected by a polyvinyl alcohol layer. The paint application process leads to differences in the thickness of the paint in different regions, which directly affects the anti-rust performance. The study reveals the deterioration mechanism of resulfurized steel components in a subtropical polluted environment and puts forward repair suggestions that consider both material compatibility and reversibility, providing a reference for the protection practice of modern and contemporary architectural metal heritage in Macau and even in similar geographical environments. Full article

To address the problem of environmental pollution caused by the extensive use of low-density polyethylene (LDPE) mulch film, this study developed a novel sprayable mulch using natural fibers and biodegradable polymers. Urea–formaldehyde resin (UF), strengthened with polyvinyl alcohol (PVA), was used as a modifier to induce beneficial physicochemical structural changes in PVA-modified urea–formaldehyde (PUF) resins. Characterization of these resins was conducted using Fourier transformation infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), and scanning electron microscopy (SEM). Preparation of the biodegradable mulch was conducted using Xuan paper waste residue (XP) as an enhancer, with PUF as the auxiliary agent. The resulting film (PUF-XP) was examined for differences in thickness, morphological characterization, and rate of weight loss, and the effects of different covering films on cucumber growth, root development, soil temperature, and weed control were evaluated. Characterization reveals that when the PVA content was 4% (W4UF), the film had the lowest free formaldehyde content (0.26%) and highest elongation at break (5.70%). In addition, W4UF could easily undergo thermal degradation at 278.4 °C and possessed a close-knit, three-dimensional structural network. W4UF was then mixed with paper powder and water in various proportions to produce three mulch films (BioT1, BioT2, and BioT3) that demonstrated excellent water retention and heat preservation and inhibited weed growth by 68.8–96.8%. Compared to no mulching (NM), BioT1 increased both the specific root length and root density, as well as improved the plant height, stem diameter, and total biomass of the cucumbers by 43.5%, 34.1%, and 33.9%, respectively. Therefore, a mass ratio of paper powder, water, and W4UF of 1:30:2 produced a biodegradable mulch film that could be used as an alternative to LDPE, mitigating the environmental pollution rendered by synthetic plastic mulch films and offering the potential for a sustainable agricultural application. Full article

Heavy metal contamination of water is a critical environmental problem due to its toxicity and persistence in ecosystems. In this study, magnetic hydrogel spheres composed of carboxymethylated starch modified with poly(1-vinylimidazole) (CMS-g-PVI) and polyvinyl alcohol (PVA), combined with Fe₃O₄ nanoparticles, were synthesized and characterized to evaluate their efficiency in adsorbing metal ions such as Cu²⁺, Pb²⁺, and Cd²⁺. Structural characterization by FT-IR spectroscopy confirmed the successful integration of all functional components into the hydrogel matrix. Additionally, scanning electron microscopy (SEM) revealed a rough and porous surface morphology favorable for adsorption and an average bead diameter of 3.2 mm, influenced by the stirring rate during synthesis. Adsorption studies demonstrated maximum capacities of 82.4 mg·g⁻¹ for Cu²⁺, 66.5 mg·g⁻¹ for Pb²⁺, and 51.8 mg·g⁻¹ for Cd²⁺, with optimal removal efficiencies at pH 6.2 and 5.7. From a theoretical perspective, density functional theory (DFT) calculations using the B3LYP/6-311+G(d,p) method allowed the optimization of molecular structures and analysis of electronic properties. The total dipole moment (TDM) of the CMS-g-PVI/PVA system reached 20.81 Debye. A significant reduction in the HOMO-LUMO energy gap was observed upon metal adsorption, with values of 0.0308 eV for Cu²⁺, 0.0175 eV for Pb²⁺, and 0.0235 eV for Cd²⁺, confirming strong interactions between the hydrogel matrix and the metal ions. The combined experimental and computational approach provides a comprehensive understanding of the adsorption mechanisms and supports the development of efficient materials for water decontamination. Full article

Hexavalent chromium (Cr(VI)), a highly toxic and carcinogenic contaminant, presents a significant hazard to aquatic ecosystems and human health. Developing environmentally friendly, cost-effective, biodegradable, and easily recyclable adsorbents is critical for efficient Cr(VI) removal. Here, we present an innovative solution using a Mg/Al layered double hydroxide (LDH)-modified sphagnum cellulose gel (MgAl/LDH@SMCG), prepared by pre-treating sphagnum cellulose, crosslinking with polyvinyl alcohol, and doping with LDH. The resulting porous composite gel features abundant -COOH and -OH chelating groups, significantly enhancing its adsorption capacity and structural stability. The material’s structure and surface modifications were systematically characterized using SEM, TGA, FT-IR, and XPS. Batch adsorption experiments were conducted to assess the influence of adsorbent dosage, initial Cr(VI) concentration, pH, contact time, and temperature on performance. Adsorption kinetics, isotherms, and thermodynamics analyses revealed a primary mechanism of monolayer chemical adsorption, with experimental data closely fitting the Freundlich isotherm and pseudo-second-order kinetic models. The modified gel exhibits increased surface roughness and adsorption sites, resulting in markedly improved Cr(VI) removal efficiency. This study not only provides theoretical insights into Cr(VI) adsorption but also highlights the potential of LDH-functionalized cellulose gels for heavy metal wastewater treatment, offering a sustainable pathway for addressing global water contamination challenges. Full article

The development of biodegradable alternatives to petroleum-based packaging is essential for environmental sustainability. This study presents a novel approach to enhance the performance of hemicellulose-based films by fabricating xylan/polyvinyl alcohol (PVA) composites reinforced with zinc oxide nanoparticles (nano-ZnO). To address nano-ZnO agglomeration, sodium hexametaphosphate (SHMP) was utilized as a dispersant, while sorbitol improved film flexibility. The composite films were prepared via solution casting, and the effects of nano-ZnO content (0–2.5 wt%) on mechanical, thermal, and barrier properties were systematically evaluated. Results showed that at 2 wt% nano-ZnO loading, the tensile strength increased from 15.0 MPa (control) to 26.15 MPa, representing a 74% enhancement, while oxygen permeability decreased from 1.83 to 0.50 (cm³·μm)/(m²·d·kPa). Additionally, the thermal stability also improved due to hydrogen bonding and uniform nanoparticle dispersion. At this optimized loading, the hydrophobcity was also maximized, with the contact angle peaking at 74.4° and water vapor permeability decreasing by 18% (1.53·10⁻⁶·g·h⁻¹·m⁻¹·Pa⁻¹). Excessive nano-ZnO loading (>2 wt%) induced particle agglomeration, generating stress concentrators that disrupted the polymer–nanoparticle interface and compromised mechanical integrity. These findings highlight the potential of nano-ZnO-modified xylan/PVA films as sustainable, high-performance alternatives to conventional packaging. The synergistic use of SHMP and nano-ZnO provides a strategy for designing eco-friendly materials with tunable properties, advancing the use of biomass in food preservation applications. Full article

Optical coherence tomography (OCT) phantoms are essential tools for calibrating imaging systems, validating diagnostic algorithms, and bridging technological advancements with clinical applications. This review explores the development and application of materials used in OCT phantoms, emphasising their optical, mechanical, and biochemical fidelity to biological tissues. Gelatin-based phantoms (n = 1.35) offer controllable absorbance and scattering, with penetration depths (PDs) of 500–2000 µm and scattering coefficients (SCs) of 5–20 cm⁻¹ but are unstable at room temperature. Silicone phantoms (n = 1.41) are durable and stable, with SCs of 10–15 cm⁻¹, suitable for long-term studies. Polydimethylsiloxane (PDMS) phantoms (n = 1.41) provide manageable optical properties and are used in microfluidic applications. Polyvinyl alcohol (PVA) phantoms (n = 1.48) mimic soft tissue mechanics, with SCs of 5–15 cm⁻¹, but require freeze–thaw cycles. Fibrin phantoms (n = 1.38) simulate blood clotting, with SCs of 5–20 cm⁻¹. Scattering particles like polystyrene (n = 1.57) and titanium dioxide (TiO₂, n = 2.49) offer modifiable properties, while silica microspheres (SiO₂, n = 3.6) and gold nanoshells (n = 2.59) provide customisable optical characteristics. These materials and particles are crucial for simulating biological tissues, enhancing OCT imaging, and developing diagnostic applications. Despite progress, challenges persist in achieving submicron resolution, long-term stability, and cost-effective scalability. Full article

The application of slow-release fertilizers is essential for improving fertilizer utilization efficiency and promoting sustainable agricultural development. Unlike traditional single organic polymer-coated or inorganic-coated fertilizers, this study utilized biodegradable modified polyvinyl alcohol (PVA) as a binder and cheap, readily available phosphogypsum–bentonite as an inorganic coating material to develop a novel slow-release potassium magnesium sulfate fertilizer (SRPMSF). This study initially examined the influence of SA dosage on PVA properties. XRD, FTIR, TGA, and water resistance analyses revealed that sodium alginate exhibits good compatibility with polyvinyl alcohol, enhancing its heat and water resistance. Ultimately, PVA–SA-2 (1.2% sodium alginate) was chosen as the optimal binder for SRPMSF production. Furthermore, this study investigated the impact of bentonite on the physical and slow-release properties of the SRPMSF by varying the phosphogypsum-to-bentonite ratio. This experiment included five treatment methods: the treatments consist of SRPMSF-1 (0 g bentonite), SRPMSF-2 (phosphogypsum/bentonite ratio of 4:1), SRPMSF-3 (3:2), SRPMSF-4 (2:3), and SRPMSF-5 (1:4). A control group (PMSF) was also included. The results indicated that, as the bentonite content increased, both the particle size and compressive strength of the coated slow-release fertilizer increased, with the SRPMSF particle sizes ranging from 3.00 to 4.50 mm. The compressive strength of the SRPMSF ranged from 20.85 to 43.78 N, meeting the requirements for industrial production. The soil column leaching method was employed to assess the nutrient release rate of the fertilizers. The experimental results indicated that, compared to the PMSF, the SRPMSF effectively regulated nutrient release. Pot experiments demonstrated that the SRPMSF significantly enhanced garlic seedling growth compared to the PMSF. In conclusion, a new type of slow-release fertilizer with good slow-release performance is prepared in this paper, which can improve the utilization rate of fertilizer and reduce the economic loss and is conducive to the sustainable development of agriculture. Full article

Copolymers of N-isopropylacrylamide (NIPA) and alkyl acrylic acids that swell and shrink in response to pH were prepared by dispersion polymerization at 35 °C using N-isopropylacrylamide (transduction monomer), methylenebisacrylamide (crosslinker), 2-dimethoxy-2-phenyl-acetophenone (initiator), N-tert-butylacrylamide (transition temperature modifier), and acrylic acid, methacrylic acid, ethacrylic acid, and propacrylic acid (functional comonomer). The diameter of the microspheres of the copolymer varied between 0.5 µm and 1.0 µm. These microspheres were cast into hydrogel membranes prepared by mixing the pH-sensitive swellable polymer particles with aqueous polyvinyl alcohol solutions followed by crosslinking the polyvinyl alcohol with glutaric dialdehyde for use as pH sensors. Large changes in the turbidity of the polyvinyl alcohol membrane monitored using a Cary 6000 UV–visible absorbance spectrometer were observed as the pH of the buffer solution in contact with the membrane was varied. Polymer swelling was reversible for many of these NIPA-based copolymers. The buffer capacity, ionic strength, pH, and temperature of the buffer solution in contact with the membrane were systematically varied to provide an in-depth pH profile of each copolymer. A unique aspect of this study was the investigation of the response of the NIPA-based polymers to changes in the pH of the solution in contact with the membrane at low buffer concentrations (0.5 mM). The response rate and the reversibility of polymer swelling even at low buffer capacity suggest that NIPA-based copolymers can be coupled to an optical fiber for pH sensing in the environment. We envision using these polymers to monitor rising acidity levels in the ocean due to water that has become enriched in carbon dioxide that endangers shell-building organisms by reducing the amount of carbonate available to them. Full article

A metal-doped modified CO oxidation catalyst with strong adsorption and water resistance for coalbed methane was prepared by the CO precipitation method. The CO ablation characteristics were tested, and the Cu Mn catalyst synthesized by metal Ce doping achieved an instantaneous ablation efficiency of 80% when in contact with CO at room temperature. By analyzing the surface crystal structure and pore characteristics, as well as by testing the ablation properties, it was found that the CO oxidation catalyst synthesized by Ce had the best effect at a precipitation temperature of 70 °C. A water-resistant CO oxidation catalyst was synthesized by adding polyvinyl alcohol (PVA) and polyvinylpyrrolidone (PVP). After storage at a relative humidity of 90%, it still had a CO adsorption rate of about 85%. The water-resistant CO oxidation catalyst prepared with polyvinyl alcohol (PVA) as an additive had a higher content of CeO₂ crystal nuclei, and the PVA-added CO oxidation catalyst had the best ablation characteristics. In the evaluation of the water-resistant steam ablation process, the CuMnO_x-Ce-PVA catalyst showed a significant increase in intermediate products during the stress process under water vapor conditions and a decrease in the peak value of the catalyst’s binding to water, and the catalyst has a particular inhibitory influence on the adsorption of water molecules on its surface. Due to its outstanding water resistance, the catalyst was able to retain good ablation characteristics. Full article

High-concentration polyvinyl alcohol (PVA) wastewater from 3D printing applications presents significant treatment challenges due to PVA’s water solubility, chemical stability, and resistance to biodegradation. In this study, we investigated the enhanced removal of high-concentration PVA (3–7 g/L) using a modified ferrite process with H₂O₂ pre-oxidation, while simultaneously exploring the formation and properties of magnetic precipitates. The effects of PVA concentration, reaction conditions, and thermal treatment (100 °C and 650 °C) on the magnetic precipitates were studied through XRD, TEM, FTIR, and magnetic measurements. Results showed that H₂O₂ pre-oxidation effectively maintained the system pH and improved PVA removal efficiency, achieving a COD reduction of 83% after two-stage treatment for 7 g/L PVA solution. XRD and TEM analyses revealed that precipitates formed at 100 °C consisted of dispersed Fe₃O₄ nanoparticles within PVA fibrous networks, while calcination at 650 °C led to the formation of rod-like structures and agglomerated particles. The magnetic properties varied significantly with treatment conditions, exhibiting the highest saturation magnetization of 10.30 emu/g for sample calcinated at 100 °C. This study demonstrates the potential of the modified ferrite process for treating high-concentration PVA wastewater while producing recoverable magnetic nanoparticles, providing a dual-function approach to address environmental challenges posed by the 3D printing industry. Full article