Search Results (27)

The presence of impurities directly affects the properties of α-hemihydrate gypsum (α-HH) prepared from phosphogypsum (PG) as a raw material. However, the effect of soluble fluorine impurities on the properties of α-HH by autoclaving remains insufficiently understood. This study investigated the influence of sodium fluoride on the morphology, hydration, and hardening properties of α-HH, using XRD, XPS, SEM, MIP, and tests of setting time, evolution of hydration temperature increase, and strength. The results showed that during the preparation of α-HH, some F⁻ reacted with Ca²⁺ to form CaF₂, which adhered to the surface of the α-HH crystal, hindering the growth and development of the crystal and resulting in small crystals with rough surfaces. When α-HH hydrated, sodium fluoride caused the early, rapid nucleation of dihydrate gypsum (DH) crystals, accelerating the crystallization process of DH. The introduction of sodium fluoride inhibited the early hydration of α-HH and promoted its later hydration. The increase in sodium fluoride content caused the initial setting time of α-HH hydration to first increase and then decrease, while the final setting time continued to decrease. In the absence of sodium fluoride, the average pore diameter of the hardened paste was approximately 617.99 nm. When the NaF content was 0.2%, the DH crystals were prismatic and densely packed, which resulted in a decrease in the average pore diameter to 449.35 nm. When the NaF content was 0.6%, the DH crystals exhibited a plate-like morphology and were loosely interlocked, leading to an increase in the average pore diameter to 1169.58 nm. Based on these results, the sodium fluoride content in PG should be controlled below 0.2%. Full article

Biofouling remains a critical challenge in membrane bioreactors (MBR), which is primarily caused by the production of extracellular polymeric substances (EPS) as an initial step in biofilm formation. This still limits their widespread application in wastewater treatment. In the past decades, much research has been carried out to understand and consequently reduce biofouling in MBR. More recent studies have focused primarily on inhibiting the release of EPS by applying quorum quenching (QQ) to control biofouling in MBR. This study presents the first investigation of the QQ potential of Rubellimicrobium mesophilum and its effects on biofilm inhibition by EPS reduction, which is demonstrated for MBR operated with submerged flat sheet (PTFE, PS) and hollow fibre polyvinylidene fluoride (PVDF) membranes operated in parallel for 114 days. The QQ effect has a significant impact on the reduction in biofilm thickness on PTFE membranes by 45% and on PS membranes by about 47%, respectively. Additionally, the performance of PVDF was improved by 287.5%. Similarly, the total protein concentration on the PTFE membranes was reduced by 57%, while on the PS membranes, the reduction was 78%. In mixed liquor, protein reduction was 55%, indicating its effectiveness in controlling biofouling over extended operation. The biofilm formation was monitored by measuring the biofilm thickness via fluorescence microscopy and by analyzing the protein and sugar content of the developing biofilm and of the mixed liquor. All parameters indicated decreasing biofilm formation with increasing amounts of entrapped QQ bacteria, while the removal efficiency of organic compounds and ammonia remained similar between all MBRs. Full article

Phosphogypsum-based cemented paste backfill (PCPB) represents an effective solution for managing substantial accumulations of PG. However, its practical application is limited by excessive fluoride content and insufficient strength. To systematically investigate the influence of initial fluoride content on the hydration behavior, microstructures, and strength development of PCPB specimens, synthetic phosphogypsum was prepared using CaSO₄·2H₂O and NaF to eliminate impurity interference in this study. A series of specimens was designed with varying initial fluoride content (5–70 mg/L), sand-to-cement ratios (1:6, 1:8, 1:10), and concentrations (63 wt%, 65 wt%). Setting time, unconfined compressive strength, isothermal calorimetry, X-ray diffraction, and scanning electron microscopy were employed to elucidate the effects and underlying mechanisms of fluoride on PCPB performance. The results indicate that higher initial fluoride content markedly delayed setting and reduced early strength. Calorimetric analysis confirmed that fluoride postponed the exothermic peak and extended the induction period, primarily due to the formation of the CaF₂ layer on clinker particle surfaces, which hindered nucleation and hydration. The microscopic results further revealed that high fluoride content suppressed the formation of ettringite and C-S-H gels, resulting in more porous and loosely bonded microstructures. Leaching tests indicated that fluoride immobilization in PCPB specimens occurred mainly through CaF₂ precipitation, physical encapsulation, and ion exchange. These findings provide theoretical support for the fluoride thresholds in PG below which the adverse effects on cement hydration and strength development can be minimized, contributing to the sustainable goals of waste reduction, harmless disposal, and resource recovery in the phosphate industry. Full article

The formation of acidic goaf water in abandoned coal mines poses significant environmental threats, especially in karst regions where the risk of groundwater contamination is heightened. This study investigates the geochemical processes responsible for the generation of acidic water through batch and column leaching experiments using coal mine surrounding rocks (CMSR) from Yangquan, China. The coal-bearing strata, primarily composed of sandstone, mudstone, shale, and limestone, contain high concentrations of pyrite (up to 12.26 wt%), which oxidizes to produce sulfuric acid, leading to a drastic reduction in pH (approximately 2.5) and the mobilization of toxic elements. The CMSR samples exhibit elevated levels of arsenic (11.0 mg/kg to 18.1 mg/kg), lead (69.5 mg/kg to 113.5 mg/kg), and cadmium (0.6 mg/kg to 2.6 mg/kg), all of which exceed natural crustal averages and present significant contamination risks. The fluorine content varies widely (106.1 mg/kg to 1885 mg/kg), with the highest concentrations found in sandstone. Sequential extraction analyses indicate that over 80% of fluorine is bound in residual phases, which limits its immediate release but poses long-term leaching hazards. The leaching experiments reveal a three-stage release mechanism: first, the initial oxidation of sulfides rapidly lowers the pH (to between 2.35 and 2.80), dissolving heavy metals and fluorides; second, slower weathering of aluminosilicates and adsorption by iron and aluminum hydroxides reduce the concentrations of dissolved elements; and third, concentrations stabilize as adsorption and slow silicate weathering regulate the long-term release of contaminants. The resulting acidic goaf water contains extremely high levels of metals (with aluminum at 191.4 mg/L and iron at 412.0 mg/L), which severely threaten groundwater, particularly in karst areas where rapid cross-layer contamination can occur. These findings provide crucial insights into the processes that drive the acidity of goaf water and the release of contaminants, which can aid in the development of effective mitigation strategies for abandoned mines. Targeted management is essential to safeguard water resources and ecological health in regions affected by mining activities. Full article

Fluoride gels are widely used in dental prophylaxis due to their proven ability to prevent demineralization and promote remineralization of hard dental tissues. However, the effectiveness of fluoride release from such gels may be significantly influenced by environmental factors such as pH and the presence of calcium ions. This in vitro study aimed to evaluate how these variables affect fluoride ion release from three commercially available fluoride gels—Clarben, Flairesse, and Lunos. The gels were incubated in artificial saliva of varying pH levels (4.5, 6.0, 7.0, and 7.5) with and without the addition of calcium, as well as in other water-based media—tap water, deionized water, and 0.9% NaCl solution. Fluoride release and changes in pH were measured and statistically analyzed using a multifactorial ANOVA. The results revealed that fluoride release was highest in calcium-free environments and at neutral to slightly alkaline pH, while the presence of calcium significantly reduced fluoride availability. Among the tested products, Flairesse and Lunos exhibited sensitivity to calcium’s presence, unlike Clarben. Fluoride release was generally higher in water than in artificial saliva. Additionally, all gels induced a decrease in pH, which varied depending on the initial pH and calcium content. These findings underline the importance of environmental conditions in optimizing the clinical efficacy of fluoride gel applications. Full article

The morphology of Poly (vinylidene fluoride) (PVDF) membranes prepared via the nonsolvent-induced phase separation (NIPS) method was modulated by altering the dope solution with citric acid (CA) and titanium dioxide nanoparticles (nano-TiO₂) to optimize the β-phase content. Three series of dope solutions were prepared in dimethyl acetamide (DMAc): (i) TONx series contained 0.0–10% citric acid, (ii) Mx series contained 0.0–0.4% nano-TiO₂, and (iii) TAx series contained 5% CA and 0.0–0.40% nano-TiO₂. A field emission scanning electron microscopy (FESEM) study revealed that CA enhances pore opening, and nano-TiO₂ transforms the sponge-like uneven porous structures into a compact, relatively regular honeycomb structure in the PVDF membranes. The combined effect of CA and nano-TiO₂ in the dope solution made the channels and chambers of the membrane well organized, and the walls of the channels transformed from solid fibrils to cross-woven nanofiber-like entities. Porosity initially peaked at 84% in the TAx series, gradually decreasing to 72% with increasing nano-TiO₂ concentrations. X-ray diffraction (XRD), Fourier-Transformed Infrared Spectroscopy (FTIR), and Differential Scanning Calorimetry (DSC) revealed the presence of a combined relative amount of the β- and γ-polymorphs of 84% in a neat PVDF membrane, 88% in an Mx, and 96% in a TAx series membrane, with the β-PVDF constituting nearly the entire portion of the combined polymorphs. The presence of 96% electroactive polymorph content in the PVDF membrane is noteworthy, highlighting its potential biomedical and industrial applications. Full article

Composite solid electrolytes are gaining interest regarding their use in Li-metal solid-state batteries. Although high ceramic content improves the electrochemical stability of ceramic-rich composite separators (C-SCE), the polymeric matrix also plays a vital role. In the first generation of C-SCE separators with a PEO-based matrix, the addition of 90–95 wt% of Li_6.45Al_0.05La₃Zr_1.6Ta_0.4O₁₂ (LLZO) does not make C-SCE stable for cell cycling with high-voltage (HV) cathodes. For the next iteration, the objective was to find an HV-stable polymeric matrix for C-SCEs. Herein, we report results on optimizing C-SCE separators with different ceramics and polymers which can craft the system towards better stability with NMC622-based composite cathodes. Both LLZO and Li_1.3Al_0.3Ti_1.7(PO₄)₃ (LATP) were utilized as ceramic components in C-SCE separators. Poly(diallyldimethylammonium) bis(trifluoromethanesulfonyl)imide (PDDA-TFSI) and poly (vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) were used as polymers in the “polymer/LiTFSI/plasticizer”-based matrix. The initial phase of the selection criteria for the separator matrix involved assessing mechanical stability and ionic conductivity. Two optimized separator formulations were then tested for their electrochemical stability with both Li metal and HV composite cathodes. The results showed that Li/NMC622 cells with LP70_PVDF_HFP and LZ70_PDDA-TFSI separators exhibited more stable cycling performance compared to those with LZ90_PEO300k-based separators. Full article

A layered double hydroxide (LDH) containing Mg and Al was synthesized from a nitrate solution using a coprecipitation method. The resulting material exhibited a homogeneous structure, which, upon calcination at 450 °C, was converted into a layered double oxide (LDO). When rehydrated in a fluoride-containing aqueous solution, the original hydroxide structure was successfully regenerated, demonstrating the LDH’s memory effect. During this transformation, fluoride anions from the solution were incorporated into the interlayer galleries to maintain electroneutrality, as confirmed by energy-dispersive X-ray spectroscopy (EDS) analysis. Separately, the process was tested in the presence of ethanol, which significantly enhanced the incorporation of fluoride ions into the interlayer spaces. The material’s potential for controlled fluoride release was evaluated by monitoring its release into demineralized water. For comparison, a simple ion-exchange process was carried out using the as-synthesized MgAl LDH. The memory effect mechanism displayed a notably higher fluoride incorporation capacity compared to the ion-exchange process. Among all the specimens, the sample reconstructed in the presence of ethanol exhibited the highest fluoride ion content. Fluoride release studies revealed a two-phase pattern: an initial rapid release within the first three hours, followed by a substantially slower release over time. Full article

Phosphogypsum (PG)-based cemented paste backfill (PCPB) is a widely used method for the large-scale disposal of phosphoric acid waste. However, fluoride contaminants in PG pose a significant risk of groundwater pollution. Effective pretreatment methods have been developed to mitigate this issue, but there is limited research on the specific pretreatment standards needed to control fluoride leaching. This study investigates the impact of initial fluoride content (IFC) in PG samples on the strength and leaching behavior of PCPB to establish appropriate pretreatment standards. Pure CaSO₄·2H₂O and NaF were used to simulate PG samples with varying IFC levels. The findings indicate that lower IFC leads to stronger PCPBs after 28 days of curing. To ensure compliance with Chinese national standards, the initial fluoride concentration must be below 0.0093 wt% to prevent excessive leaching. Microlevel analyses reveal that fluoride influences the hydration reactions of C₂S and C₃S in cement, affecting the formation of C-S-H and Ca(OH)₂. Fluoride is primarily immobilized in PCPB as CaF₂, which can either form gypsum crystals within the complex structure or be adsorbed onto hydration products. This research provides crucial insights into the pretreatment standards required for controlling fluoride leaching, offering a foundation for the industrial application of PG. Full article

Due to its acidic nature and high fluoride concentration, hydrated lime (Ca(OH)₂) is commonly used for neutralization and fluoride control in semiconductor wastewater treatment. This study investigated the efficacy of treating high fluoride-containing wastewater using hydrated lime derived from oyster shells as an alternative to limestone. Overall, the characteristics of removing pollutants in acidic wastewater using shell-based hydrated lime showed similar patterns to hydrated lime from limestone. The treatment efficiency was 50% or less under theoretical Ca/F molar ratio (=0.5) conditions for the formation of fluorite (CaF₂), while the fluorine removal rate reached 99% under somewhat higher Ca/F conditions due to the influence of ionic components in the wastewater. Interestingly, chloride content did not increase even in the initial reaction stages, in contrast to our concerns about oyster shells generally containing salt to a certain extent due to their growth in seawater; instead, the chloride concentration decreased over time, similar to nitrate (NO₃⁻). In controlling fluoride in wastewater, surpassing the theoretical Ca/F molar ratio, particularly considering the presence of other anionic species such as SO₄^²− and PO₄³⁻, the optimal Ca/F ratio for fluoride removal was found to be 1.59. This value is approximately 16% lower than the calculated value (Ca/F = 1.85) when accounting for other anions. X-ray diffraction results confirmed the presence of CaSO₄, Ca₃(PO₄)₂, and CaF₂ in the precipitate recovered after the reaction, indicating the effective removal of ionic contaminants. This observation suggests that oyster shell-derived hydrated lime could serve as a viable calcium resource for treating acidic wastewater and represents a potential alternative to traditional limestone-based methods. Full article

Low concentrations of fluoride (F⁻) in drinking water are beneficial for oral health, but the natural occurrence of high F⁻ content has been reported in various groundwater sources, posing a continuous ingestion threat to humans. The utilization of biochar (BC) produced from residual biomass has emerged as a technically, economically, and environmentally sustainable alternative for fluoride removal through adsorption. Therefore, this study aimed to investigate the physicochemical characteristics of BC derived from coffee grounds and the influence of various factors on the adsorption process of F⁻ in aqueous media, including pH, adsorbent dosage, contact time, temperature, and initial F⁻ concentration. The BC exhibited a surface area of 12.94 m²·g⁻¹ and a pore volume of 0.0349 cm³·g⁻¹. The adsorption process was strongly pH dependent, demonstrating a significant decline in performance as pH increased from 2.0 onwards. The majority of F⁻ removal occurred within the first 5 min, reaching adsorption equilibrium after 1 h of testing, regardless of the initial F⁻ concentration employed. The data fitting to the Webber–Morris model indicated a two-step adsorption process on BC, with the first step being external surface sorption and the second step being intra-articular diffusion. The process was determined to be endergonic, and the data satisfactorily matched both the Freundlich and Langmuir models, with a q_m of 0.53 mg·L⁻¹ (T = 55 °C), indicating the predominance of physisorption. The findings suggest the potential of coffee grounds for BC production; nevertheless, surface structure modifications are necessary to enhance F⁻ affinity and subsequently improve adsorption capacity. Full article

Secondary caries is one of the leading causes of resin-based dental restoration failure. It is initiated at the interface of an existing restoration and the restored tooth surface. It is mainly caused by an imbalance between two processes of mineral loss (demineralization) and mineral gain (remineralization). A plethora of evidence has explored incorporating several bioactive compounds into resin-based materials to prevent bacterial biofilm attachment and the onset of the disease. In this review, the most recent advances in the design of remineralizing compounds and their functionalization to different resin-based materials’ formulations were overviewed. Inorganic compounds, such as nano-sized amorphous calcium phosphate (NACP), calcium fluoride (CaF₂), bioactive glass (BAG), hydroxyapatite (HA), fluorapatite (FA), and boron nitride (BN), displayed promising results concerning remineralization, and direct and indirect impact on biofilm growth. The effects of these compounds varied based on these compounds’ structure, the incorporated amount or percentage, and the intended clinical application. The remineralizing effects were presented as direct effects, such as an increase in the mineral content of the dental tissue, or indirect effects, such as an increase in the pH around the material. In some of the reported investigations, inorganic remineralizing compounds were combined with other bioactive agents, such as quaternary ammonium compounds (QACs), to maximize the remineralization outcomes and the antibacterial action against the cariogenic biofilms. The reviewed literature was mainly based on laboratory studies, highlighting the need to shift more toward testing the performance of these remineralizing compounds in clinical settings. Full article

Fluoride is one of the main phytotoxic environmental pollutants, and high concentrations (10–30 mg L⁻¹) are commonly detected in surface and groundwater. Little, however, is known about the effects of this pollutant on crops that require irrigation during their development, which, in addition to phytotoxicity, may cause negative human health effects. Thus, the aim of this study was to characterize the effects of potassium fluoride (KF) on the germination of lettuce seeds and identify the physiological and anatomical markers of this pollutant’s action on plants exposed to it during growth. Initially, lettuce seeds were sown in gerboxes and soaked in solutions containing 0 mg L⁻¹, 10 mg L⁻¹, 20 mg L⁻¹, and 30 mg L⁻¹ KF. Plants grown in a greenhouse were treated daily with KF irrigation at the same KF concentrations for 40 days. KF exposure reduced the germination rate and germination speed index of lettuce seeds at 20 mg L⁻¹ and 30 mg L⁻¹, resulting in compromised root development at the highest KF concentration. Lettuce plants displayed a slight photosynthesis reduction and a significant photochemical efficiency decrease after exposures to all KF concentrations. Lower chlorophyll contents and nitrogen balance indices were observed in plants exposed to 30 mg L⁻¹ KF. On the other hand, increases in phenolic compounds and malondialdehyde were noted with increasing KF concentrations. Lettuce plants can, therefore, accumulate fluoride in leaves when irrigated with KF-rich water. The investigated physiological and biochemical variables were proven to be adequate fluoride action biomarkers in lettuce plants and may become an important tool in the study of olericulture contaminants. Full article

The enamel white spot lesion is a common complication of orthodontic treatment with a high prevalence. This research aims to create an artificially induced white spot lesion, evaluate three different commercial products in terms of visual appeal, mineral reestablishment, and roughness, and determine which material can recover the initial structure. We created an artificially induced white spot lesion in extracted teeth. The materials used in the study were peptide p11-4 (CurodontTM Repair, Credentis AG), bioactive glass toothpaste (Biomin F, BioMin Technologies Limited), and local fluoridation (Tiefenfluorid, Humanchemie) in conjunction with low-level laser therapy (LLLT). To objectively assess the surface, the roughness, mineral content, and esthetic were measured. The roughness increased with a median difference of −0.233 µm in the bioactive glass group; the color parameter delta L decreased dramatically with a median difference of 5.9–6.7; and the cervical third increased the Ca-P mineral content above the starting stage. Each material contributed significantly to enamel consolidation, with peptide therapy providing the most encouraging results. Full article

Nanocomposites of poly (vinylidene fluoride) PVDF with graphene nanoflakes (GNF) were prepared using two different routes. Initially, a mix-melting method was used to prepare composites, and their thermal and mechanical properties were evaluated to choose the better method for future experiment and properties investigation. Then, nanocomposite films were prepared by a simple solution-casting technique using a PVDF/graphene solution. In both cases, the amount of graphene was varied to observe and to compare their thermal and mechanical properties. The addition of graphene to the PVDF matrix resulted in changes in the crystallization and melting behaviors as confirmed by DSC analyses. Increasing the graphene content led to improved thermal stability of the PVDF nanocomposites prepared using both methods. Improvements in mechanical properties by the addition of graphene were also observed. Better performance was observed by the nanocomposites prepared by a mix-melting technique suggesting better dispersion and strong interface bonding between PVDF and graphene particles. Thermal and electrical conductivity were measured and compared. Microstructure and morphology were characterized using FTIR, XRD, and SEM analyses. Full article