Search Results (60)

Background/Objectives: This study investigated how selected functionality-related characteristics (FRCs) of hypromellose (HPMC)—namely viscosity, hydroxypropoxy substitution, particle size, and the ratio of water-soluble (FlowLac^® 100) to water-insoluble (Avicel^® PH-102) fillers— affect the release of carvedilol from matrix tablets. Methods: Using a Central Composite Design (CCD) Design of Experiments (DoE), mixtures of HPMC QbD samples were prepared to achieve target HPMC FRC levels. Within the CCD, levels of FlowLac^® 100 and Avicel^® PH-102 were also varied. The mean and standard deviation of carvedilol release at each analyzed time point of the release profile were used as target variables for individual multiple linear regression (MLR) models. Results: Lactose, the water-soluble filler, significantly accelerated carvedilol release, whereas the water-insoluble MCC slowed and stabilized release by improving gel integrity. Among the HPMC FRCs, particle size had the strongest influence during the early release phase, while HPMC viscosity and hydroxypropoxy substitution degree became more important in later phases. Analysis of the results using optimized multiple linear regression (MLR) models revealed key interaction effects, particularly between HPMC viscosity and lactose content, and between viscosity and particle size, demonstrating their combined role in modulating release kinetics. Conclusions: These findings provide valuable insight into how controlling HPMC’s FRCs and filler composition can reduce interbatch variability in drug release and support the rational design of robust controlled release formulations. Full article

This study prepared alkali-activated cementitious composites using high-whiteness kaolin, sodium water glass, and NaOH as the main raw materials. Multiple methods, including FE-SEM, XRD, whiteness/light transmittance tests, shrinkage rate measurements, DSC-TG, flexural strength testing, and hydrolysis resistance testing, were used to investigate the effects of curing temperature and time on material properties. The optimal parameters were determined as kaolin calcined at 1100 °C, activator modulus 1.25, calcined kaolin-to-activator ratio 1:1, and 2.5% deionized water added for molding. The optimal sample achieved a flexural strength of 23.81 MPa, with the bonding strength to porcelain 60.17 times that of gypsum and 1.90 times that of kaolin-bonded materials. Curing below 100 °C slowed polymerization, while temperatures exceeding 100 °C accelerated it, with violent reaction at 120 °C. Curing beyond 10 h reduced flexural strength. A large number of cage-like, ‘zeolite-like’ structures formed, closely relating to material properties. This study provides references for ceramic restoration materials. Full article

Graphene quantum dots (GQDs) obtained by microwave-induced pyrolysis of glutamic acid and triethylenetetramine (trien) are fairly stable, emissive, water-soluble, and positively charged nano-systems able to interact with negatively charged meso-tetrakis(4-sulfonatophenyl) porphyrin (TPPS₄). The stoichiometric control during the preparation affords a supramolecular adduct, GQDs@TPPS₄, that exhibits a double fluorescence emission from both the GQDs and the TPPS₄ fluorophores. These supramolecular aggregates have an overall negative charge that is responsible for the condensation of cations in the nearby aqueous layer, and a three-fold acceleration of the metalation rates of Cu²⁺ ions has been observed with respect to the parent porphyrin. Addition of various metal ions leads to some changes in the UV/Vis spectra and has a different impact on the fluorescence emission of GQDs and TPPS₄. The quenching efficiency of the TPPS₄ emission follows the order Cu²⁺ > Hg²⁺ > Cd²⁺ > Pb²⁺ ~ Zn²⁺ ~ Co²⁺ ~ Ni²⁺ > Mn²⁺ ~ Cr³⁺ >> Mg²⁺ ~ Ca²⁺ ~ Ba²⁺, and it has been related to literature data and to the sitting-atop mechanism that large transition metal ions (e.g., Hg²⁺ and Cd²⁺) exhibit in their interaction with the macrocyclic nitrogen atoms of the porphyrin, inducing distortion and accelerating the insertion of smaller metal ions, such as Zn²⁺. For the most relevant metal ions, emission quenching of the porphyrin evidences a linear behavior in the micromolar range, with the emission of the GQDs being moderately affected through a filter effect. Deliberate pollution of the samples with Zn²⁺ reveals the ability of the GQDs@TPPS₄ adduct to detect sensitively Cu²⁺, Hg^2+, and Cd²⁺ ions. Full article

Recycled wood fiber (RWF) obtained through the multi-stage processing of waste wood serves as an eco-friendly green construction material, exhibiting lightweight, porous, and high toughness characteristics that demonstrate significant potential as a cementitious reinforcement, offering strategic advantages for environmental protection and resource recycling. In this study, high-performance sulfoaluminate cement (SAC)-RWF composites prepared by modifying RWFs with nano-silica (NS) and a silane coupling agent (KH560) were developed and their effects on mechanical properties, shrinkage behavior, hydration characteristics, and microstructure of SAC-RWF composites were systematically investigated. Optimal performance was achieved at water–cement ratio of 0.5 with 20% RWF content, where the KH560-modified samples showed superior improvement, with 8.5% and 14.3% increases in 28 d flexural and compressive strength, respectively, compared to the control groups, outperforming the NS-modified samples (3.6% and 8.6% enhancements). Both modifiers improved durability, reducing water absorption by 6.72% (NS) and 7.1% (KH560) while decreasing drying shrinkage by 4.3% and 27.2%, respectively. The modified SAC composites maintained favorable thermal properties, with NS reducing thermal conductivity by 6.8% through density optimization, whereas the KH560-treated specimens retained low conductivity despite slight density increases. Micro-structural tests revealed accelerated hydration without new hydration product formation, with both modifiers enhancing cementitious matrix hydration product generation by distinct mechanisms—with NS acting through physical pore-filling, while KH560 established Si-O-C chemical bonds at paste interfaces. Although both modifications improved mechanical properties and durability, the KH560-modified SAC composite group demonstrated superior overall performance than the NS-modified group, providing a technical pathway for developing sustainable, high-performance recycled wood fiber cement-based materials with balanced functional properties for low-carbon construction applications. Full article

This study aimed to investigate the effect of dip coating and the composition of the applied coating on the structure and sorption properties of freeze-dried carrot bars. The scope of the work included preparing freeze-dried carrot bars, coating them with coatings of different gelatin concentrations, and then analysing the sorption properties based on sorption isotherms. Additionally, the structure was assessed based on porosity, shrinkage, and microscopic observations. Water activity and dry matter content were also measured. Analysis of the obtained results showed that coating caused a significant increase in water activity and a decrease in the dry matter content of freeze-dried carrot bars. There was also a decrease in porosity and volume compared to the control sample, which was confirmed by microscopic analysis. The study of sorption kinetics showed that the coatings limited the hygroscopicity of the samples, reducing the dynamics of moisture adsorption and accelerating the stabilisation of water content. The best model describing the sorption isotherms was the Peleg model, and the isotherms themselves were classified as type IIb according to the Blahovec and Yanniotis classification. The composition of the coating significantly affects the structure and selected physical properties of the bars. FT-IR analysis did not show any significant changes in the bars’ chemical structure. Full article

Traditional tomato-braised beef brisket with potatoes is celebrated for its rich, complex flavors and culinary appeal but requires lengthy preparation. Pre-packaged versions of the dish rely on thermal sterilization for safety; however, high-temperature processing accelerates protein and lipid oxidation, thereby compromising its sensory quality. As the demand for ready-to-eat meals grows, the food industry faces the challenge of ensuring microbial safety while preserving flavor integrity. In this study, low-temperature plasma sterilization (LTPS) (160 KV, 450 s) was evaluated as a non-thermal alternative to conventional high-temperature short-time (HSS) sterilization. Furthermore, a comprehensive analysis was conducted over a 10-day storage period, assessing microbial viability, physicochemical properties (pH, shear force, and water-holding capacity), oxidative markers (TBARS, TVB-N, and protein carbonyls), volatile compounds (GC-MS), and electronic nose (e-nose) responses. The results revealed that LTPS (160 kV, 450 s) successfully maintained bacterial counts below regulatory limits (5 lg CFU/g) for 72 h, ensuring that the microbial indicators of short-term processed products sold to supermarkets through cold chain logistics were in the safety range. Additionally, LTPS-treated samples showed a 4.2% higher water-holding capacity (p < 0.05) during storage, indicating improved preservation of texture. Furthermore, LTPS-treated samples exhibited 32% lower lipid oxidation (p < 0.05) and retained 18% higher sulfhydryl content (p < 0.05) compared to HSS, indicating reduced protein oxidation. GC-MS and e-nose analyses showed that LTPS preserved aldehydes and ketones associated with meaty aromas, while HSS contributed to sulfur-like off-flavors. Principal component analysis showed that the LTPS samples had shorter distances across various storage periods compared to HSS, indicating reduced differences in aroma difference. The findings of this study demonstrate LTPS’s dual efficacy in microbial control and aroma preservation. The technology presents a viable strategy for extending the shelf life of pre-prepared meat dishes while reducing oxidative and flavor deterioration, thereby establishing a solid foundation for LTPS application in the pre-prepared food sector. Full article

Cemented paste backfill (CPB) improves underground stability by filling mine voids, but the high cost of cement presents economic challenges for miners. While alternative binders and admixtures have been explored, the combined impact of slag substitution and alkali-free (AF) accelerators on CPB performance is not yet fully understood. This study investigates the influences of slag substitution and AF accelerators on the performance of CPB through a comprehensive experimental approach. CPB samples were prepared with slag substitution ratios of 25%, 50%, and 75%, maintaining a fixed AF accelerator content of 0.4%. Various test techniques, including unconfined comprehensive strength (UCS), mercury intrusion porosimetry (MIP), X-ray diffraction (XRD), and thermal analysis (TG/DTA), were employed to study their mechanical and microstructural properties. Monitoring tests were also conducted to thoroughly assess the performance of CPB, including suction (self-desiccation), electrical conductivity (EC), and volumetric water content (VWC) tests. The results showed that the PCI50–SL50–0.4AF sample exhibited 2.3 times higher strength than the control sample for 28 days, with this improvement attributed to enhanced pozzolanic reactions contributing to better microstructural compactness. Monitoring tests revealed accelerated hydration kinetics and reduced water content in slag-reinforced CPB, highlighting the significant role of AF accelerator in facilitating rapid setting and improving early-age mechanical strength. Microstructural findings revealed that porosity decreased and C–S–H gel formation increased in the specimen containing slag and AF accelerators, contributing to increased strength and durability. These findings highlight the potential usage of slag and AF accelerators to enhance CPB’s mechanical, microstructural, and hydration properties, offering significant benefits for mining operations by improving backfill performance, while contributing to environmental sustainability through reduced cement consumption and associated CO₂ emissions. Full article

Developing biodegradable complex fertilizers is crucial for sustainable agriculture to reduce the environmental impact of mineral fertilizers and enhance soil quality. This study evaluated chitosan-based hydrogel coatings for sodium alginate matrices encapsulating amino acid hydrolysates from mealworm larvae, known for their plant growth-promoting properties. The research aims to identify the potential of biopolymer matrices for producing biodegradable slow-release fertilizers and to outline future development pathways necessary for this technology to be usable in the fertilizer industry. Chitosan coatings prepared with citric acid and crosslinked with ascorbic acid optimized plant growth, while those using acetic acid negatively affected it. Water absorption and nutrient release tests showed that chitosan coatings reduced water uptake and slowed initial nutrient release compared to uncoated samples. Leaching assays confirmed controlled-release behavior, with an initial burst followed by stability, driven by alginate–chitosan interactions and ion exchange. The X-ray diffraction (XRD) analysis revealed that adding hydrolysate and chitosan increased amorphousness and reduced porosity, improving structural properties. Thermogravimetric analysis (TGA) and Fourier-transform infrared (FTIR) spectroscopy demonstrated enhanced homogeneity and the presence of chemical interactions, which led to improvements in the material’s thermal stability and chemical characteristics. Biodegradation tests indicated greater durability of chitosan-coated composites, although hydrolysate incorporation accelerated decomposition due to its acidic pH. Germination tests confirmed no phytotoxicity and highlighted the potential of biopolymeric matrices for slow nutrient release. These findings indicate the possibilities of chitosan-coated alginate matrices as sustainable fertilizers, emphasizing the importance of adjusting coating composition and hydrolysate pH for enhanced efficacy and environmental benefits. The main recommendation for future research focuses on optimizing the chitosan coating process by exploring whether adding hydrolysate to the chitosan solution can reduce diffusional losses. Additionally, investigating the use of glycerol in the alginate matrix to minimize pore size and subsequent losses during coating is suggested. Future studies should prioritize analyzing percentage losses during the crosslinking of the alginate matrix, chitosan coating, and final shell crosslinking. This pioneering research highlights the potential for encapsulating liquid fertilizers in biopolymer matrices, offering promising applications in modern sustainable agriculture, which has not been studied in other publications. Full article

With the acceleration of urbanization, clay with significant variations in organic matter content is commonly encountered in infrastructure construction. Its unique water retention capacity is crucial for engineering safety and stability. This study uses red clay as the matrix and incorporates peat to prepare soil samples with varying organic matter content. Soil–water characteristic tests were conducted using the pressure plate method, filter paper method, and vapor equilibrium method to obtain the soil–water characteristic curves across the entire suction range. Subsequently, scanning electron microscopy (SEM) and mercury intrusion porosimetry (MIP) tests were performed to analyze the mechanisms underlying the water retention characteristics. The experimental results indicate that the three different suction tests accurately reflect the soil–water characteristic curves of organic clay across the entire suction range. As the organic matter content in the soil increases, the air entry value and residual value of the soil samples exhibit a linear relationship with the organic matter content, enhancing the soil’s water retention capacity. The increase in organic matter content alters the microstructure of the clay, transforming the mineral–organic aggregates from ellipsoidal to plate-like shapes. While organic matter can influence the water retention of clay, within a certain suction range, the water retention capacity of organic clay is also related to the pore structure and the state of water within the pores. This is crucial for ensuring engineering safety and optimizing design solutions. Full article

A series of hydrophilic copolymers were prepared using 2-hydroxyethyl methacrylate (HEMA) and itaconic acid (IA) from free radical polymerization at different feed monomer ratios using ammonium persulfate (APS) initiators in water at 70 °C. The herbicide 2,4-dichlorophenoxy acetic acid (2,4-D) was grafted to Poly(HEMA-co-IA) by a condensation reaction. The hydrolysis of the polymeric release system, Poly(HEMA-co-IA)-2,4-D, demonstrated that the release of the herbicide in an aqueous phase depends on the polymeric system’s pH value and hydrophilic character. In addition, the swelling behavior (Wt%) was studied at different pH values using Liquid-phase Polymer Retention (LPR) in an ultrafiltration system. The acid hydrolysis of the herbicide from the conjugates follows a first-order kinetic, showing higher kinetic constants as the pH increases. The base-catalyzed hydrolysis reaction of the herbicide follows a zero-order kinetic, where the basic medium acts as a catalyst, accelerating the release rate of the herbicide and showing higher kinetic constants as the pH increases. The differences in the release rates found for the hydrogel herbicide at different pH values can be correlated with the difference in their swelling capacity, where the release rate generally increases with an increase in the swelling capacity from water solution at higher pH values. The study of the release process revealed that all samples in distilled water at a pH of 10 are representative of agricultural systems. It showed first-order swelling kinetics and an absorption capacity that conforms to the parameters for hydrogels for agricultural applications, which supports their potential for these purposes. Full article

Background/Objectives: Hydroxypropyl methylcellulose (HPMC) is one of the most commonly used hydrophilic polymers in formulations of matrix tablets for controlled release applications. However, HPMC attracts moisture and poses issues with drug stability in formulations containing moisture-sensitive drugs. Methods: Herein, the moisture sorption behavior of excipients and drug stability using aspirin as the model drug in matrix tablets were evaluated, using HPMC and the newly developed mannitol-coated HPMC, under accelerated stability conditions (40 °C, 75% relative humidity) with open and closed dishes. Results: Tablets prepared with mannitol-coated HPMC showed a slower drug degradation rate compared to tablets prepared with directly compressible HPMC. Initial moisture content and hygroscopicity were stronger predictors of drug stability compared to water activity when comparing samples without similar moisture content. In the early stage (day 0 to 30), the aspirin degradation rate was similar in both open and closed conditions, as moisture content is the main degradation contributor. In the later stage (day 30 to 90), aspirin degradation was faster under closed conditions than under open conditions, likely due to autocatalytic effects caused by the volatile acidic by-product entrapped in the closed environment. Conclusions: The findings from this study reinforced the importance of judicious excipient selection based on the understanding of excipient–moisture interactions to maximize the chemical stability of moisture-sensitive drugs. Mannitol-coated HPMC is a promising addition to the formulator’s toolbox for the formulation of controlled release dosage forms by direct compression. Full article

The poor properties of recycled coarse aggregate (RCA) and recycled coarse aggregate concrete (RCAC) are considered key constraints hindering the reuse of this waste resource in marine engineering. The CO₂-based accelerated carbonation method, which utilizes the alkali aggregate properties of RCA to achieve CO₂ uptake and sequestration while significantly enhancing its properties, has attracted widespread attention. However, the degree of improvement in the properties of RCA under different initial moisture conditions (IMCs) and aggregate particle sizes (APSs) after CO₂-accelerated carbonation remains unclear. Moreover, the quantitative effect of carbonated recycled coarse aggregate (CRCA), which is obtained from RCA samples with the optimal initial moisture conditions, on the improvement of RCAC under optimal accelerated carbonation modification conditions still needs to be studied in depth. For this investigation, a CO₂-accelerated carbonation experiment was carried out on RCA samples with different IMCs and APSs, and the variations in the properties of RCA with respect to its IMC and APS were assessed. The degree of accelerated carbonation modification of RCA under different IMCs and APSs was quantified, and the optimal initial moisture conditions for enhancing the properties of the RCA were confirmed. By preparing concrete specimens based on the natural coarse aggregate, RCA, and CRCA with the best initial moisture conditions (considering the same concrete–water proportion), the effect of CRCA on the workability, mechanical properties, and durability of the corresponding concrete specimen was determined. The findings of this study can be used to effectively promote the sustainable development of marine science and engineering in the future and contribute to global dual-carbon goals, which are of great practical significance and scientific value. Full article

In recent years, oxygen vacancy (V_O) engineering has become a research hotspot in the field of photocatalysis. Herein, an efficient GQDs/BiOCl-V_O heterojunction photocatalyst was fabricated by loading graphene quantum dots (GQDs) onto BiOCl nanosheets containing oxygen vacancies. ESR and XPS characterizations confirmed the formation of oxygen vacancy. Combining experimental analysis and DFT calculations, it was found that oxygen vacancy promoted the chemical adsorption of O₂, while GQDs accelerated electron transfer. Benefiting from the synergistic effect of oxygen vacancy, GQDs, and dye sensitization, the as-prepared GQDs/BiOCl-V_O sample exhibited improved efficiency for RhB degradation under visible-light irradiation. A 2 wt% GQDs/BiOCl-V_O composite effectively degraded 98% of RhB within 20 min. The main active species were proven to be hole (h⁺) and superoxide radical (·O₂⁻) via ESR analysis and radical trapping experiments. This study provided new insights into the effective removal of organic pollutants from water by combining defect engineering and quantum dot doping techniques in heterojunction catalysts. Full article

Zinc alumotitanate sorbents with various compositions were prepared through sol-gel synthesis with the use of ethyl acetoacetate as a chelating agent. The formation and decomposition of chelates, providing insight into sol-gel process advancement, have been successfully monitored via ¹H NMR, ¹³C NMR, and FTIR spectroscopy. It has been established that Al(OBu^s)₃ and Ti(OBuⁿ)₄ react completely with Eaa, forming chelates after 1 h, while after 24 h hydrolysis is already advanced. Hydrolysis is accelerated in the presence of Zn(NO₂)₃·6H₂O, supplying the water needed for hydrolysis. In dried gels, the amount of ethyl acetoacetate is greatly reduced, and it is mainly present unbound. According to XRD analysis, samples with none or less titania are composed of layered double hydroxide, while in samples with greater amounts of titania, crystal nitrates are present. In all samples except those without Al, the spinel phase with variable composition crystallizes. Full article

For the dry storage of Canada Deuterium Uranium (CANDU) spent nuclear fuels, the integrity of Zircaloy-4 fuel cladding has to be verified. However, the formation of ~10 µm-thick oxide layers in typical CANDU reactor operating conditions takes several years, which makes sample preparation a slow process. To overcome such limitations, in this study, an accelerated formation of an oxide layer on Zircaloy-4 cladding tube was developed with a combination of high-temperature water corrosion (HT-WC) and air oxidation (AO). First, Zircaloy-4 tubes were corroded in oxygenated (2 ppm dissolved oxygen) high-temperature water (360 °C/19.5 MPa) for 500 h. Then, the tubes were air-oxidized at 500 °C for 30 h. Finally, the tubes were corroded again in HT-WC for 500 h to produce ~10 µm-thick oxide layers. The morphology and characteristics of the oxide layer in each step were analyzed using X-ray diffraction, scanning and transmission electron microscopy. The results showed that the oxide layer formed in the accelerated method was comparable to that formed in HT-WC in terms of morphology and oxide phases. Thus, the accelerated oxide formation method can be used to prepare an oxidized Zircaloy-4 cladding tube for CANDU fuel integrity analysis. Full article