Search Results (824)

The treatment of olive mill wastewater (OMW) remains a major environmental challenge due to its high organic load and phenolic content. This study investigates a combined approach using lime pretreatment and limestone (LS)-based adsorption for cost-effective and sustainable OMW remediation. Locally sourced limestone was used in both micro- and nanoscale forms, while lime (CaO) was produced by calcination. The materials were characterized using X-ray Diffraction pattern (XRD), Scanning Electron Microscopy (SEM), Brunauer–Emmett–Teller (BET), and Point of Zero Charge (pH_PZC) analyses to evaluate surface properties relevant to adsorption. Lime pretreatment achieved notable reductions in total suspended solids (TSS, 99%), chemical oxygen demand (COD, 43%), and total phenolic content (TPC, 48%). Subsequent adsorption with nano-limestone (particles obtained through high-energy ball milling, followed by sieving, with a size distribution 400–500 nm) further enhanced pollutant removal, achieving up to 72% COD and 89% TPC reduction in batch experiments. Column studies confirmed the synergistic effect of mixed particle sizes, yielding 65% COD and 76% TPC removal. The combined process demonstrates the potential of lime–limestone composites as locally available and eco-friendly materials for OMW treatment. While promising, the results represent laboratory-scale findings; further optimization and long-term assessments are recommended for field applications. Full article

Phenolic compounds are regarded as one of the components responsible for olive oil’s functional properties and health benefits. These chemicals act as antioxidants and anti-inflammatories, and prevent chronic diseases. The Folin–Ciocalteu reagent or HPLC procedures are commonly used to determine the concentration of total phenolic compounds in olive oil. The use of ethyl lactate or lactic acid ethyl ester (LAEE) instead of methanol (MeOH) was examined in terms of green chemistry. Six extra virgin olive oils (EVOOs) with phenolic content ranging from 20 to 350 mg/L, were first extracted with 1:4, 2:3, 3:2, 4:1, and 5:0 MeOH or LAEE/water, (v/v), to determine total phenolic content (TPC) and antiradical activity (%RSA) using the Folin–Ciocalteu reagent and DPPH assay, respectively. The concentration of extracted phenolics or extracts’ RSA increased as the water content in the organic solvent mixture decreased. Also, TPC values were greater when extracted with LAEE than MeOH, while the differences were modest. The HPLC profiles of EVOO phenolic extracts produced by 4:1 MeOH or LAEE/water, (v/v), were indistinguishable in principal component analysis. Simplification of the phenolic profile via acid hydrolysis, resulting in increased hydroxytyrosol and tyrosol content liberated from the corresponding bound forms, showed that both organic solvents equally recovered the predominating phenols of the polar fraction. A noted limitation of LAEE extraction is the need for freeze-drying to remove it prior to HPLC analysis of aqueous extracts. Nonetheless, these findings support LAEE as an effective and environmentally friendly alternative to MeOH for EVOO phenolic extraction in both analytical and industrial contexts. Full article

The effectiveness of periodate-assisted photocatalysis in removing the cationic dye Safranin O (SO) was evaluated using a UV/TiO₂/IO₄⁻ process operated at room temperature under near-neutral pH conditions. Under base conditions ([IO₄⁻] = 0.15 mM, [TiO₂] = 0.4 g/L, [SO] = 10 mg/L), the ternary system achieved a pseudo-first-order rate constant of 0.6212 min⁻¹, outperforming the UV/TiO₂ and UV/IO₄⁻ processes by approximately 21- and 29-fold, respectively. This yielded a synergy ratio of about 12 compared to the sum of the binary processes. Targeted quenching experiments revealed the operative pathways. Strong inhibition by ascorbic acid and phenol indicates that interfacial holes and ^•OH are key oxidants. Methanol caused a moderate slowdown, consistent with ^•OH and hole scavenging. Benzoquinone and oxalate suppressed removal by intercepting the electron and O₂^•− pathways, respectively. Dichromate markedly inhibited the process via optical screening and competition for electrons. Azide had little effect, suggesting a minor role for singlet oxygen. Matrix studies showed progressively slower kinetics from deionized water to mineral water to seawater. This was due to halides, sulfate, alkalinity, and TiO₂ aggregation driven by ionic strength. Additional tests confirmed that the dominant modulators of performance were humic acid (site fouling and light screening), chloride and sulfate (radical speciation and surface effects), nitrite (near-diffusion radical quenching), and bicarbonate at pH 8.3 (conversion of ^•OH to CO₃^•−). Nonionic surfactants (Tween 80, Triton X-100) also depressed SO removal through micellar sequestration and competitive adsorption on TiO₂. The study confirms the potential of UV/TiO₂/IO₄⁻ as a tunable AOP capable of delivering rapid and reliable dye degradation under a wide range of water quality conditions. The mechanistic mapping unifies two roles for IO₄⁻, an electron acceptor that inhibits recombination and a photochemical precursor of iodine centered and ^•OH radicals and connect these roles to the observed synergy and to the trend across deionized water, mineral water, and seawater. The scavenger outcomes assign the main oxidant flux to holes and ^•OH radicals with a contributory electron or O₂^•− branch from IO₄⁻ reduction. Full article

This study explores chitosan (CS)-based materials for water purification, assessing their disinfection and contaminant degradation capabilities. A reproducible protocol was developed to fabricate homogeneous, stable CS films, validated through permeability testing and characterized using thermal (TGA), mechanical (tensile strength, elongation), and physico-chemical (FTIR-ATR, water contact angle, SEM-EDX) analyses. A catalyst was employed to complex iron ions and crosslink CS chains via acrylamide functions, stabilizing the CS structure and reducing washout in water. Disinfection tests showed that pure CS exhibited strong antimicrobial activity under varying contamination levels, attributed to direct contact and slight dissolution. Functionalized CS materials acted as catalytic surfaces, requiring hydrogen peroxide (H₂O₂) to generate reactive oxygen species (ROS). This ROS-mediated process effectively disinfected high bacteria loads and degraded phenol. Electron paramagnetic resonance (EPR) confirmed hydroxyl radicals as the primary active species when H₂O₂ was present. Under lower contamination levels, residual CS within the functionalized material contributed to direct antimicrobial effects, demonstrating a synergistic action between CS and ROS. These findings highlight CS as a reliable disinfectant and functionalized CS as a versatile material for ROS-driven antimicrobial action and contaminant degradation. The results suggest potential for scalable, sustainable water treatment applications. Future work will focus on optimizing the catalyst structure to enhance ROS production and improve contaminant removal efficiency. Full article

It is generally found that enhancement in catalytic activity comes at the expense of selectivity or stability. In this study, an SO_x²⁻-modified Mn₂O₃ (SO-Mn₂O₃) solid catalyst was prepared using a simple oxalate precipitation method. This catalyst exhibited not only high catalytic activity but also high selectivity and good cycling stability. The degradation ratio of bisphenol A (BPA) under SO-Mn₂O₃ activated potassium peroxymonosulfate (PMS) achieved over 99% within 10 min, and the mineralization ratio increased to 83.2%. Particularly, the degradation rate for BPA under the SO-Mn₂O₃/PMS system was 15 times that of Mn₂O₃. Furthermore, the degradation ratio remained at 93.3% after five consecutive cycles. Multiple experimental characterizations confirmed that the introduction of SO_x²⁻ into Mn₂O₃ shifted the oxidative degradation pathway from a mixture of radical and non-radical routes to a predominantly non-radical pathway. This suppressed radical generation promoted the selective formation of high-valence metallic-oxo (Mn(V)=O) species and singlet oxygen (¹O₂), thereby significantly enhancing the catalytic activity. In addition, the SO-Mn₂O₃/PMS system exhibited broad applicability towards the degradation of other phenolic pollutants, strong anti-interference capability against complex water matrices, and suitability for efficient removal of organic contaminants in such environments. This research offers new perspectives for the design of selective catalysts for PMS activation. Full article

Plant-derived wastes are increasingly explored as organic matter sources for sustainable agriculture. Tea waste, a by-product of industrial tea processing, is often regarded as an environmental pollutant, yet its potential for agricultural use remains conditional and requires careful evaluation. This study examined the effects of factory-derived tea waste on kale (Brassica oleracea var. acephala) under drought stress. Plants were grown in soils amended with 5% or 10% tea waste and subjected to mild (75% field capacity) and moderate (50% field capacity) water deficits, compared with full irrigation (100% field capacity). Fifteen morphological and physiological parameters were assessed, and data were analyzed using principal component analysis (PCA) and correlation heatmaps to identify trait associations and stress markers. Drought stress significantly reduced all growth and yield traits, with stronger effects under more severe water deficit. Tea waste generally exacerbated stress impacts, increasing damage indices, reducing plant height, and lowering chlorophyll values. However, 10% tea waste under non-stress conditions increased plant and root dry weights without negatively affecting other traits, suggesting a partial nutrient contribution. In contrast, 5% tea waste aggravated stress effects, likely due to phenolic and caffeine toxicity. Overall, raw tea waste was found to be unsuitable for kale production under drought conditions. To harness its potential, bioactive compounds must be degraded or removed, and the material stabilized through composting or biochar conversion for safe integration into drought-resilient systems. Full article

Bentonites used for wine clarification vary widely in their ability to remove proteins and alter wine composition, yet the role of their intrinsic properties remains unclear. To address this, eight commercial bentonites with diverse physico-chemical characteristics were analyzed. The doses required for complete protein removal and stabilization were determined and then applied to clarify a Malvazija istarska (Vitis vinifera L.) white wine. Clarified wines were compared with one another and with a non-clarified control using ICP-OES for elemental composition, HPLC-DAD for phenolic compounds, and HS-SPME-GC/MS for volatile compounds. Protein removal efficiency correlated positively with Na/Ca ratio, cation exchange capacity, swelling capacity, negative ζ-potential, and internal specific surface area, and negatively with particle size and external specific surface area. Sodium and calcium showed the greatest increases in wine concentrations. Effects on individual low-molecular-weight phenols were inconsistent, though all bentonites removed a fraction of total phenols. Volatile compounds, particularly esters, were significantly reduced. When compared on a per-gram basis, bentonites that were more efficient in protein removal also showed greater removal of phenols and volatile compounds; however, at full application doses, many of these differences diminished or reversed. Overall, the study advances understanding of bentonite–wine interactions and supports more informed selection of bentonites in oenological practice. Full article

The inefficient disposal of corn stover (CS) and the accumulation of magnesite tailings (MMTs) pose dual environmental threats. Although biomass gasification can utilize CS, its inherent drawbacks result in syngas with low heating value and high tar content. Torrefaction pretreatment can effectively improve biomass properties, and the use of steam as a reaction medium can further optimize the product’s pore structure. This study proposes a steam-assisted torrefaction pretreatment to address the inefficient utilization of CS and the disposal challenges of MMTs. The experimental results demonstrated that torrefaction at 300 °C with 30% water content for 60 min significantly improved the raw material’s properties. The optimized CSBC exhibited a well-developed pore structure and achieved a phenol removal rate of 63.4%. The addition of MMTs further enhanced the pretreatment effect, increasing the removal rate to 75.5% and confirming the superiority of the CSBC–magnesite composite system. The steam atmosphere improved phenol adsorption by regulating pore structures and surface functional groups, offering a feasible approach for utilizing solid waste resources and developing a new in situ tar control strategy. Full article

This study conducted a systematic investigation of the degradation pathway and process optimization of strong acid cation exchange resins subjected to SCWO. Controlled experiments evaluated the effects of operating temperature, oxidant stoichiometry, initial organic concentration, and residence time. RSM was utilized to refine the operating parameters, and a second-order regression model (R² = 0.9951) was established to predict COD removal (R_COD), valid within experimental ranges: reaction temperature 400–500 °C, oxidant stoichiometry 80–150%, initial COD 10,000–100,000 mg·L⁻¹, and residence time 1–10 min. COD-dependent NaOH addition could enhance degradation efficiency. The R_COD was sensitive to operating temperature, oxidant stoichiometry, and residence time. Under the optimized conditions of 472 °C, oxidant stoichiometry of 137%, initial COD of 77,216 mg·L⁻¹, and residence time of 4.9 min with the addition of 1.74 wt% NaOH, the R_COD reached 99.92%, which was in close agreement with model predictions. GC-MS analysis of intermediates revealed that sulfonic groups dissociated early, followed by aromatic compounds, particularly phenol, undergoing ring-opening and oxidation to small carboxylic acids and aliphatic species, which were ultimately mineralized to CO₂ and H₂O. These findings provide mechanistic insight into resin decomposition and offer a scientific basis for the safe treatment of radioactive waste resins using SCWO. Full article

This study explores a hybrid advanced electrochemical oxidation process (EAOP) intensified by solar irradiation and ozone for the treatment of wastewater containing COVID-19-related pharmaceuticals. Pilot-scale trials were performed in a 30 L compound parabolic collector (CPC)-type photoreactor with a boron-doped diamond (BDD–BDD) electrode configuration. Under optimal conditions (50 mg L⁻¹ paracetamol, 0.05 M Na₂SO₄, 0.50 mM Fe²⁺, pH 3.0, and 60 mA cm⁻²), the solar photoelectro-Fenton (SPEF) process achieved 78% chemical oxygen demand (COD) reduction within 90 min, with catechol and phenol detected as the main aromatic intermediates. When applied to a four-drug mixture (dexamethasone, paracetamol, amoxicillin, and azithromycin), the solar photoelectro-Fenton (SPEF–ozone (O₃)) system reached 60% degradation and 41% COD removal under solar conditions. The results highlight the synergistic effect of ozone and solar energy in enhancing the electrochemical oxidation process (EAOP) performance and demonstrate the potential of these processes for scalable and sustainable removal of pharmaceutical contaminants from wastewater. Full article

Phenolic compounds constitute the predominant group of recalcitrant organic contaminants in coal chemical wastewater. In this study, humic acid and urea were used as carbon and nitrogen sources to prepare nitrogen-doped carbon material (labeled as NC-800) through a two-step calcination process. Using this catalyst (NC-800) to activate PMS for phenol degradation achieved 100% phenol removal across a wide pH range (1–9). The removal rate remained at 99.62% even with high concentrations of inorganic anions or natural organic matter, breaking through the limitations of traditional Fenton-like reactions in terms of acid–base environment and anion influence. The quenching experiment and electron spin resonance (ESR) spectroscopy results indicated that the N-C/PMS system generated three active species hydroxyl radicals (•OH), superoxide radicals (O₂^•−), and singlet oxygen (¹O₂) through the active sites in electron-rich regions such as graphite nitrogen, pyrrole nitrogen, and C=O. An electrochemical test revealed that the system formed a metastable NC-800-PMS* complex during the reaction, indicating the existence of a non-radical pathway of electron transfer. The combination of free radicals (•OH, O₂^•−) and non-free radicals (¹O₂, electron transfer) facilitated the rapid degradation of phenol, providing a theoretical basis for phenol degradation. Full article

The study compared the effects of conventional and vegan processing aids in the clarification of must, focusing on the phenolic and sensory characteristics of must and wine. The hypothesis was that plant protein could provide results similar to those of conventional aids containing proteins of animal origin, especially in aromatic grapes, where hyperoxidation is avoided. Conducted in 2024 in Etyek-Buda, Hungary, the initial trials subjected the Irsai Olivér grape must to gravity sedimentation with various agents. Vegan processing aids, notably the combination of pea protein and chitin-glucan, showed a gentle impact on the assimilable nitrogen content and a similar reduction in turbidity to those with animal proteins. Nitrogen flotation trials compared gelatin and the vegan alternative (a combination of pea protein and chitin–glucan) in Irsai Olivér and Chardonnay must clarification. The removal of phenolic substances was monitored using the Folin–Ciocalteu method, the acid butanol assay, and the vanillin assay. In addition, nitrogen levels were evaluated before and after the flotation experiments. The plant-based processing aid effectively improved the sensory quality of Irsai Olivér. However, the gelatin-treated Chardonnay was fresher and less bitter than the vegan option, which was less balanced and more bitter with weaker aroma and flavor. Full article

Hydroethanolic Cucurbita pepo seed extracts are traditionally used for alleviating lower urinary tract symptoms (LUTS), yet their mechanisms remain unclear. Adenosine, a purine nucleoside involved in neuromodulation and smooth muscle relaxation, was recently identified in C. pepo seeds. Since A₁ adenosine receptors (A₁AR) suppress parasympathetic bladder overactivity by inhibiting acetylcholine (ACh) release, we investigated to which extent purines from pumpkin seed extracts contribute to A₁AR activation. Complementary antioxidant capacity was assessed using the 2,2-diphenyl-1-picrylhydrazyl (DPPH) assay. Three hydrophilic seed extracts containing different adenosine levels (0.60–1.18 mg/g dw) were evaluated for agonist activity using a cAMP inhibition assay. The most active extract showed an EC₅₀ of 40.22 µg/mL. Selective removal of adenosine shifted the dose–response curve rightward, while further elimination of an adenosine derivative increased the EC₅₀ to 212.10 µg/mL, confirming adenosine as the principal active compound. Guanosine and inosine did not exhibit A₁AR agonist or allosteric effects. All samples exhibited measurable but weak antioxidant activity (IC₅₀ = 1.02–4.19 mg/mL), consistent with their low total phenolic content. These findings underscore the importance of accounting for naturally occurring agonists in plant extracts to avoid overestimating receptor-mediated effects in vitro which are not translatable in vivo. Full article

Heavy metal pollutants and organic contaminants often co-exist in the environment, posing significant ecological risks due to their combined toxicity. Phytoremediation, a plant-based biotechnology, offers a promising solution for pollutant removal. This study investigated the potential cadmium (Cd) removal capacity of Narrow Crown Black-Cathay poplar (Populus × canadensis Moench × Populus simonii Carr. f. fastigiata Schneid.) under combined Cd-phenol stress. The results showed that the combined stress synergistically inhibited the photosynthetic physiological characteristics, with an inhibition rate up to 54.0%, significantly higher than that under single stress (p < 0.05). Cd accumulation varied markedly among plant organs, following the order: root (ranging from 4000.2 to 9277.0 mg/kg) > stems (ranging from 96.0 to 383.6 mg/kg) > leaf (ranging from 10.3 to 40.1 mg/kg). Phenol enhanced Cd absorption and enrichment in the roots by up to 1.8 times but reduced its translocation to aboveground parts by 37.8–40.0%. Notably, at low Cd concentrations, the Cd removal efficiency under combined stress (26.0%) was substantially higher than under single Cd stress (6.6%). In contrast, biomass, tolerance index, and root–shoot ratio were slightly affected in all treatments (p > 0.05). These findings demonstrate that Narrow Crown Black-Cathay poplar is a suitable candidate for the short-term remediation of Cd in environments co-contaminated with cadmium and phenol. Full article

Sonochlorination (US/chlorine) is an emerging sonohybrid advanced oxidation process whose performance reportedly surpasses that of its individual components. However, the underlying oxidant budget is still being debated. We mapped the mechanism by systematically probing the US/chlorine system with selective scavengers (ascorbic acid, nitrobenzene, tert-butanol, 2-propanol, and phenol), competing anions (nitrite), and natural organic matter (humic acid). The kinetic hierarchy US/chlorine > US > chlorine remained consistent across all conditions, though its magnitude depended heavily on the matrix composition. Efficient ^•OH traps, such as alcohols and nitrobenzene, only partially suppressed the US/chlorine system. However, they greatly slowed sonolysis. This reveals a substantial non-^•OH channel in the hybrid process. Ascorbic acid eliminated synergy by stoichiometrically removing free chlorine. Phenol quenched HOCl and chlorine-centered radicals. Nitrite imposed a dual penalty by scavenging ^•OH and consuming HOCl via the nitryl chloride (ClNO₂) pathway. Humic acid acted as a three-way sink for ^•OH, HOCl, and chlorine radicals. These patterns suggest that reactivity is co-controlled by Cl^•, Cl₂^•−, and ClO^•. The results obtained are mechanistically consistent with cavitation-assisted activation of HOCl/OCl⁻ at pH 5–6, where HOCl concentration is maximal. This yields a mixed oxidant suite in which Cl₂^•− is the dominant bulk oxidant, Cl^• provides fast interfacial initiation, and ClO^• offers selective support. Full article