Search Results (273)

Background: This study investigated a new multi-acid-etching formulation for zirconia ceramics, containing hydrochloric, hydrofluoric, nitric, orthophosphoric, and sulfuric acids. The solution was tested on polycrystalline (5Y-TZP zirconia), lithium disilicate, hybrid ceramic, and feldspathic porcelain to assess compatibility, etching selectivity, and surface conditioning. Methods: Two-hundred-and-forty CAD/CAM specimens were etched for 20 s, 60 s, 30 min, or 1 h, and their surface roughness and etching patterns ware evaluated using 3D optical profilometry and scanning electron microscopy (SEM). Results: A positive correlation was observed between etching time and surface roughness (Ra values). The most pronounced changes were observed in lithium disilicate and feldspathic porcelain, with Ra values increasing from 0.733 ± 0.082 µm (Group 5) to 1.295 ± 0.123 µm (Group 8), and from 0.902 ± 0.102 µm (Group 13) to 1.480 ± 0.096 µm (Group 16), respectively. Zirconia increased from 0.181 ± 0.043 µm (Group 1) to 0.371 ± 0.074 µm (Group 4), and the hybrid ceramic from 0.053 ± 0.008 µm (Group 9) to 0.099 ± 0.016 µm (Group 12). Two-way ANOVA revealed significant effects of material and etching time, as well as a significant interaction between the two factors (p < 0.001). SEM observation revealed non-selective etching pattern for the lithium disilicate groups, indicating a risk of over-etching. Conclusions: The tested etching solution increased surface roughness, especially for the lithium disilicate and feldspathic porcelain specimens. In zirconia, one-hour etching improved surface characteristics with minimal observable damage. However, additional studies are necessary to validate the mechanical stability and bond effectives of this approach. Full article

Hydrogen sulfide (H₂S) can be produced from the metabolism of foods containing sulfur in the gastrointestinal tract (GIT). At low doses, H₂S regulates the gut microbial community and supports GIT health, but depending on dose, age, and individual health conditions, it may also contribute to inflammatory responses and gut barrier dysfunction. Controlling H₂S production in the GIT is important for maintaining a healthy gut microbiome. However, research on this subject is limited due to the gaseous nature of the chemical and the difficulty of accessing the GIT in situ. In the present ex vivo experiment, we used a single-dose sodium sulfide preparation (SSP) as a H₂S precursor to test the effect of H₂S on the human gut microbiome across different age groups, including breastfed infants, toddlers, adults, and older adults. Metagenomic sequencing and metabolite measurements revealed that the development of the gut microbial community and the production of short-chain fatty-acids (SCFAs) were age-dependent; that the infant and the older adult groups were more sensitive to SSP exposure; that exogeneous SSP suppressed SCFA production across all age groups, except for butyrate in the older adult group, suggesting that H₂S selectively favors specific gut microbial processes. Full article

Reducing the application of chemical fertilizers and remediating heavy metal pollution in soil are important directions in current agricultural research. Utilizing the plant-growth-promoting and remediation capabilities of bacteria can provide more environmentally friendly assistance to agricultural production. In this study, the Burkholderia alba YIM B08401 strain was isolated and identified from rhizospheric soil, subjected to whole-genome sequencing and analysis, and its Cd²⁺ adsorption efficiency and characteristics were confirmed using multiple experimental methods, including atomic absorption spectrometry (AAS), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDS). The results showed that the genome of strain YIM B08401 has a total length of 7,322,157 bp, a GC content of 66.39%, and predicts 6504 protein-coding sequences. It contains abundant functional genes related to nutrient conversion (phosphate solubilization, sulfur metabolism, zinc solubilization, siderophore production), plant hormone regulation (indole-3-acetic acid secretion, ACC deaminase production), phenolic acid degradation, root colonization, heavy metal tolerance, pathogen antagonism, and the production of antagonistic secondary metabolites. Additionally, strain YIM B08401 can specifically bind to Cd²⁺ through various functional groups on the cell surface, such as C-O-C, P=O, and O-H, enabling biosorption. In conclusion, strain YIM B08401 is an excellent strain with plant-growth-promoting, disease-resistant, and bioremediation capabilities, warranting further development as a biofertilizer for agricultural applications to promote green and sustainable agricultural development. Full article

Odors from pet cats can negatively affect the quality of life of cat owners. The diverse bioactive compounds in plant extracts make them a promising candidate for effective odor reduction. This study evaluated twelve plant extracts for deodorizing efficacy via in vitro fermentation tests. Rosemary extract and licorice extract exhibited better deodorizing effects, with fractions of rosemary extract below 100 Da demonstrating the most effective deodorizing performance. Based on these findings, subsequent feeding trials were conducted using rosemary extract and its fractions below 100 Da. In the feeding trial, adult British Shorthair cats were divided into three groups (Control Check, RE, and RE100) and housed in a controlled-environment respiration chamber for 30 days. Measurements included odor emissions, fecal and blood physicochemical parameters, immune parameters, microbiota composition based on 16S rRNA sequencing, and metabolome analysis. The results of the feeding trial indicated that rosemary extract significantly reduced ammonia and hydrogen sulfide emissions (46.84%, 41.64%), while fractions below 100 Da of rosemary extract achieved even greater reductions (55.62%, 53.87%). Rosemary extract regulated the intestinal microbial community, significantly increasing the relative abundance of the intestinal probiotic Bifidobacterium (p < 0.05) and reducing the population of sulfate-reducing bacteria (p < 0.05). It also significantly reduced urease and uricase activities (p < 0.05) to reduce ammonia production and inhibited the degradation of sulfur-containing proteins and sulfate reduction to reduce hydrogen sulfide emissions. Furthermore, rosemary extract significantly enhanced the immune function of British Shorthair cats (p < 0.05). This study suggests that rosemary extract, particularly its fractions below 100 Da, is a highly promising pet deodorizer. Full article

Modified nano-clays, alone or combined with probiotics, may offer a novel and sustainable approach to improve ruminal fermentation and mitigate CH₄ emissions in high-fiber diets. This study evaluated the properties and effects of modified nano-bentonite (MNB), with or without yeast (Saccharomyces cerevisiae), compared to natural bentonite (NB) and monensin, using the in vitro gas production (GP) technique. The substrate used was a basal diet composed primarily of forage (Trifolium alexandrinum clover) in a 70:30 forage-to-concentrate ratio. The treatments were a control group receiving the basal diet without additives; a monensin-added diet containing 40 mg/kg of dry matter (DM); a yeast-added diet with Saccharomyces cerevisiae at 2 × 10⁸ CFU/g of DM; a NB clay-added diet at 5 g/kg of DM; and MNB diets added at two levels (0.5 g/kg of DM (MNB_Low) and 1 g/kg of DM (MNB_High)), with or without S. cerevisiae. MNB showed a smaller particle size and improved properties, such as higher conductivity, surface area, and cation exchange capacity, than NB. Sulfur and related functional groups were detected only in MNB. No differences were observed in total GP, while both the monensin diet and the MNB_High-with-yeast diet significantly reduced CH₄ emissions compared to the control (p < 0.05). The MNB_High-without-yeast combination significantly (p < 0.05) reduced hemicellulose degradation, as well as total protozoal counts, including Isotricha and Epidinium spp. (p < 0.05), compared to the control. Ammonia levels did not differ significantly among treatments, while NB and MNB_High diets tended to have (p = 0.063) the highest short-chain fatty acid (SCFA) concentrations. These findings suggest the potential modulatory effects of yeast and MNB on rumen fermentation dynamics and CH₄ mitigation. Full article

This study investigates the potential of sulfuric acid modified wheat straw, polysaccharide-rich agricultural byproduct, as a low-cost adsorbent for the selective adsorption of Au(III) ions from aqueous solutions. The wheat straw was treated with concentrated sulfuric acid to enhance its surface properties and functional groups, particularly sulfonic and oxygen-containing functional groups. Adsorption experiments were performed under various conditions, including acid concentrations ranging from 1.0 to 3.0 mol/L, contact times from 1 to 6 h, and initial Au(III) concentrations of 60.36, 90.0, and 150.0 mg/L. The highest adsorption efficiency, 99.0%, was achieved at an acid concentration of 1.0 mol/L. Furthermore, it was determined that an increase in the initial Au(III) concentration from 60.36 mg/L to 150.0 mg/L resulted in a 4.5 times increase in maximum adsorption capacity under optimal conditions. Kinetic modeling revealed that the adsorption process followed pseudo-second order kinetics, suggesting chemisorption as the rate-limiting step. Characterization techniques such as SEM/EDS, XRD, BET and XPS confirmed structural modification, surface sulfonating, and the successful adsorption and reduction of Au(III) to elemental gold (Au⁰) on the modified straw surface. This work demonstrates that modified wheat straw is a promising, effective, and low cost for the recovery of gold from low-concentration solutions and provides insight into the adsorption and reduction mechanisms at the molecular level. Full article

In designing an optimized activated carbon-based adsorbent, several key factors are crucial for its practical application in the industrial sector, including high BET surface area, strong adsorption capacity, selectivity, mechanical and thermal stability, regeneration potential, environmental impact, and cost-effectiveness. This study explores the innovative approach of combining two chemical activating agents, potassium carbonate and sodium thiosulfate, to produce activated carbon with enhanced properties for improved mercury removal. At an activation temperature of 800 °C, the resulting adsorbent achieved a BET surface area of 2132.7 m²/g and a total pore volume of 1.08 cm³/g. Testing its mercury removal efficiency, the maximum adsorption capacity was 289 mg/g at room temperature. The Langmuir isotherm provided an excellent fit to the experimental data, indicating a monolayer adsorption process. Kinetic modeling revealed that the adsorption followed a pseudo-second-order model, consistent with chemisorption. The primary removal mechanism was found to involve complexation of mercury with oxygen and sulfur-containing functional groups, along with pore-filling physical adsorption. The adsorbent also showed a strong affinity for mercury even in the presence of other competing heavy metals. Furthermore, regeneration studies demonstrated the adsorbent’s effectiveness over five cycles. This research introduces a novel, environmentally friendly, and cost-efficient adsorbent for mercury removal. Full article

Türkiye hosts a wide variety of barite deposits that can be broadly classified into two major groups based on their tectonic settings: magmatism-associated and passive margin-hosted deposits. The magmatism-associated deposits include Kızılcaören (F + Ba + REE + Th, Beylikova–Eskişehir), Kirazören (Bulancak–Giresun), and Karacaören (Mesudiye–Ordu). The Kızılcaören deposit formed in relation to the emplacement of a late Oligocene carbonatitic sill, while the Kirazören and Karacaören deposits are associated with the Cretaceous Pontide magmatic arc. Passive margin-hosted deposits occur within various Paleozoic sedimentary lithologies—such as metasandstone, shale, schist, and limestone—and are found in the Taurides and the Arabian Platform. These deposits occur as either concordant or discordant veins. This barite belt extends from Şarkikaraağaç (Isparta), through Hüyük (Konya) and Alanya (Antalya), to Silifke (Mersin), Tordere (Adana), Önsen, Şekeroba (Kahramanmaraş), and Hasköy (Muş). The Paleozoic deposits represent the major barite resources of Türkiye, with an annual production of approximately 300,000 metric tons. Smaller deposits around Gazipaşa (Antalya) contain minor Pb-Zn sulfides. Mesozoic barite deposits are hosted in Triassic dolomites and are associated with Pb-Zn mineralization in the Hakkari region of the Arabian Platform. Pb and Sr isotope data indicate that the barium in these deposits was derived from ancient continental crust. The isotopic compositions of both concordant (stratabound) and discordant (vein-type) barites are generally homogeneous. In northwestern Türkiye, the Sr isotope compositions of the barite deposits align well with those of the Oligocene carbonatite host complex. The ⁸⁷Sr/⁸⁶Sr isotope ratio of the Kızılcaören deposit (0.706‰) is the least radiogenic among Turkish barite deposits, suggesting a mantle contribution. The Kirazören deposit in the Pontide magmatic arc follows with a slightly higher ratio (0.707‰). Triassic barites from the Hakkari region yield ⁸⁷Sr/⁸⁶Sr values around 0.709‰, slightly more radiogenic than coeval seawater. Paleozoic barite deposits show the most radiogenic ⁸⁷Sr/⁸⁶Sr values, including Aydıncık (0.718‰), Şarkikaraağaç (0.714‰), Hasköy (0.713‰), Kahramanmaraş (0.712‰), Tordere, and Hüyük (both 0.711‰), consistent with their respective host rocks. The elevated radiogenic Pb and Sr isotope values in the passive margin-hosted deposits suggest that the barium originated from deeper, barium-enriched rocks, whereas stable sulfur isotope data point to a marine sulfur source. Moreover, Sr and S isotopic signatures indicate that the Paleozoic sediment-hosted deposits formed in association with cold seeps on the seafloor, resembling modern analogs. In contrast, the Mesozoic Karakaya deposit (Hakkari) represents a typical vent-proximal, sediment-hosted deposit with no magmatic signature. Full article

Heavy metal pollution, especially from Pb(II) and Cd(II), poses significant risks due to its persistence and bioaccumulation potential. Traditional removal methods face challenges like high costs and secondary pollution. This study developed a novel three-dimensional porous adsorbent XBS, derived from xanthate-modified Phanerochaete sordida YK-624 (a white-rot fungus), for the rapid and efficient removal of Pb(II) and Cd(II) from wastewater. Characterization showed that XBS has a sponge-like structure with abundant functional groups, significantly enhancing its adsorption capacity and kinetics. XBS achieved 96% Pb(II) and 32% Cd(II) removal within 1 min at a 0.25 g/L dose, reaching over 95% of the maximum adsorption capacity within 30 min for Pb(II) and 240 min for Cd(II). The maximum capacities were 224.72 mg/g for Pb(II) and 82.99 mg/g for Cd(II). Kinetic and thermodynamic analyses indicated a chemisorption-driven process, which was both endothermic and spontaneous. XBS exhibited high selectivity for Pb(II) over Cd(II) and other metals (Tl(I), Cu(II)), attributed to stronger covalent interactions with sulfur- and nitrogen-containing groups. Mechanistic analyses (XRD, FTIR, and XPS) revealed that removal occurs via ion exchange, complexation, and precipitation, forming stable compounds like PbS/CdS and PbCO₃/CdCO₃. Given its cost-effectiveness, scalability, and high efficiency, XBS represents a promising adsorbent for heavy metal remediation, particularly in Pb(II)-contaminated wastewater treatment applications. Full article

The aim of this study is to determine the characteristics of the chemical and mineral composition of sediment layers in a technogenic settling pond. This pond is located on urban land in Berezniki (Perm Krai, Russia), outside the territory of operating industrial facilities, and contains alkaline saline industrial wastes. The origin of this waste was related to sludge from the Solvay soda production process, which had been deposited in this pond over a long period of time. However, along with the soda waste, the pond also received wastewater from other industries. As a result, the accumulated sediment is characterized by variation in morphological properties both in depth and laterally. Five undisturbed columns were taken to study the composition of the accumulated sediment. The obtained samples were analyzed by X-ray diffraction (XRD), synchronous thermal analysis (STA), and X-ray fluorescence (XRF) analysis. The results showed that the mineral composition of bottom sediments in each layer of all studied columns is characterized by the predominance of calcite precipitated from wastewater. Along with calcite, due to the presence of magnesium and sodium in the solution, other carbonates precipitated—dolomite and soda (natron), as well as complex transitional carbonate phases (northupite and trona). Together with carbonate minerals, the chloride salts halite and sylvin, sulfate minerals gypsum and bassanite, and pyrite and nugget sulfur were established. The group of terrigenous mineral components is represented by quartz, feldspars, and aluminosilicates. The chemical composition of sediments in the upper part of the section generally corresponds to the mineral composition. In the lower sediment layers, the role of amorphous phase and non-mineral compounds increased, which was determined by the results of thermal analysis. The content of heavy metals and metalloids also increases in the middle and lower sediment layers. When categorized according to the Igeo value, an excessive degree of contamination (class 6) was observed in all investigated columns for copper content (Igeo 5.2–6.1). Chromium content corresponds to class 5 (Igeo 4.1–4.6), antimony to class 4 (Igeo 3.0–4.0), and lead, arsenic, and vanadium to classes 2 and 3 (moderately polluted and highly polluted). The data obtained on variations in the mineral and chemical composition of sediments represent the initial information for the selection of methods of accumulated waste management. Full article

This study evaluated the chemical composition and subcutaneous tissue biocompatibility of C-Point, a root canal filling material, compared to ProTaper gutta-percha cones (control). Material characterization was conducted using scanning electron microscopy with energy-dispersive spectroscopy (SEM-EDS). For biocompatibility assessment, both materials were implanted subcutaneously in the dorsal connective tissue of sixteen albino rats (n = 8 per group). Histological evaluation of inflammatory infiltrate intensity was performed at 30 and 60 days post-implantation, with statistical analysis (significance set at p < 0.05). SEM-EDS analysis revealed distinct elemental compositions: C-Point primarily contained zirconium and cobalt ions, while gutta-percha cones demonstrated a strong zinc signature with trace amounts of barium, aluminum, and sulfur. Both materials exhibited similar particulate morphology with radiopaque inclusions. Histologically, no significant difference in inflammatory response was observed between C-Point and gutta-percha at any time point (p > 0.05). All specimens developed a fibrous encapsulation. The inflammatory profile showed temporal dynamics, with lymphocyte predominance during early stages that progressively diminished by the study endpoint. These findings demonstrate that while C-Point possesses a unique elemental profile dominated by zirconium, its tissue biocompatibility parallels that of conventional gutta-percha obturation materials. However, due to the absence of mechanical testing and the limited in vivo follow-up period, the long-term stability of the material remains uncertain. Full article

The development of polymer binders with tailored functionalities and green manufacturing processes is highly needed for high-performance lithium–sulfur batteries. In this study, a readily hydrolyzable 3,9-divinyl-2,4,8,10-tetraoxaspiro-[5.5]-undecane is utilized to prepare a water-based binder. Specifically, the acrolein produced by hydrolysis undergoes in situ polymerization to form a linear polymer, while the other hydrolyzed product, pentaerythritol, physically crosslinks these polymer chains via hydrogen bonding, generating a network polymer (BTU). Additionally, gallic acid (GA), a substance derived from waste wood, is further introduced into BTU during slurry preparation, forming a biphenol-containing binder (BG) with a multi-hydrogen-bonded structure. This resilience and robust cathode framework effectively accommodate volumetric changes during cycling while maintaining efficient ion and electron transport pathways. Furthermore, the abundant polar groups in BG enable strong polysulfide adsorption. As a result, sulfur cathode with a high mass loading of 5.3 mg cm⁻² employing the BG (7:3) binder still retains an areal capacity of 4.7 mA h cm⁻² after 50 cycles at 0.1 C. This work presents a sustainable strategy for battery manufacturing by integrating renewable biomass-derived materials and eco-friendly aqueous processing to develop polymer binders, offering a green pathway to high-performance lithium–sulfur batteries. Full article

Antioxidants, such as stilbenes, anthocyanidins, coumarins, tannins and flavonoids, are often based on oxygen-containing redox systems and tend to feature several hydroxyl groups in their chemical structures. From a synthetic perspective, oxygen atoms are prone to bioisosteric replacement with sulfur and, notably, selenium. The main objective of this narrative literature review is to explore if and how bioisosteric substitution of oxygen with sulfur or selenium can enhance the biological activity of natural products. This replacement boosts the biological activity of the resulting molecules considerably as they now combine the redox and antioxidant properties of the original flavonoids and other natural products with the specific redox behavior of sulfur and selenium. Besides sequestering free radicals and peroxides, they may, for instance, also catalyze the removal of oxidative stressors, capture free metal ions and even provide scope for selenium supplementation. Since these molecules resemble their natural counterparts, they also exhibit considerable selectivity inside the body and a good pharmacokinetic profile. Still, the synthesis of such hybrid molecules integrating sulfur and selenium into flavonoids and other natural products is a challenge and requires innovative synthetic strategies and approaches. Full article

A series of novel fluorescent donor–acceptor–donor (D-A-D) dyes containing [1,2,5]oxadiazolo[3,4-d]pyridazine and its 1-oxide as electron-withdrawing groups has been synthesized and thoroughly investigated using X-ray diffraction and molecular spectroscopy methods. This study showed that the introduction of N-oxide into the 1,2,5-oxadiazole ring in the acceptor fragment leads to a significant decrease in the luminescence intensity and quantum yield of the dyes. A comprehensive comparison of the photophysical properties of the obtained compounds containing the 1,2,5-oxadiazole ring with the previously studied [1,2,5]thia- and 1,2,5-selenadiazolo[3,4-d]pyridazine analogs showed that the oxygen substitution in the acceptor fragment shifts the phosphorescence maximum from the NIR region of 980–1100 nm to the red region of 690–770 nm. In contrast, for oxygen- and sulfur-containing dyes, purely red fluorescence with a maximum in the spectral range of 620–900 nm is observed. The crystal structures of furoxan-containing 3d·½CHCl₃ and furazan-containing 4d exhibit a non-planar [1,2,5]oxadiazolo[3,4-d]pyridazine fragment. We have found that short non-covalent interactions of the furoxan system with a lattice chloroform molecule in 3d lead to luminescence quenching. Meanwhile, in the 4d dye, the intermolecular π-π interactions of pyridazine nitrogen atoms with the N-carbazolyl group of the adjacent molecule should facilitate intermolecular charge transfer (ICT) emission. Thus, the luminescence maxima for these dyes can be tuned across a broad range of 700–1100 nm by varying the number of chalcogen atoms, highlighting the potential for tailoring optical properties in optoelectronic applications. Full article

The preparation of stable dispersions of MoS₂ by ultrasonic aqueous and/or organic media containing amphiphilic molecules is an attractive and widely applicable method to form MoS₂ fine particles while suppressing its aggregation. In this study, we developed a series of polymers with pendant sulfide moieties as a new dispersant, under the hypothesis that it would interact with sulfur atoms on MoS₂ surfaces. First, we designed a sulfide group-substituted methacrylate derivative (ESMA) with the hypothesis that it would interact with the MoS₂ surface through sulfur-sulfur interactions. Then, we synthesized well-defined polymers with pendant sulfide groups by living radical polymerization (ATRP). Next, 0.5 wt% MoS₂ was added to a DMSO solution containing 1 wt% of the obtained polymer (polyESMA), and the mixture was treated with a bath-type ultrasonicator for 3 h to obtain a MoS₂ dispersion. We found that stable dispersions of MoS₂ in a fine particle state, although not in the form of single-layer or few-layer nanosheets, could be readily formed in DMSO using polyESMA as a polymeric dispersant. Furthermore, we synthesized polymeric dispersants with different molecular weights and investigated the relationship between the structure of the dispersant and the dispersion stability. Full article