Search Results (63)

Rouaite (Cu₂(OH)₃NO₃) long hexagonal multilayered nanoplates with high purity and high crystallinity were prepared from acidic reaction solution (pH = 4.4–4.8) with the assistance of ZnO. The ZnO-assisted strategy is remarkably different from the conventional synthetic protocol that was regularly carried out in alkaline solution (pH > 11). The rouaite multilayer nanoplates displayed exceptionally high catalytic activity in the catalytic wet peroxide oxidation (CWPO) of Congo red (CR). The catalytic efficiency for CR decolorization achieved an impressive 96.3% in 50 min under near-neutral (pH = 6.76) and ambient conditions (T = 20 °C, p = 1 atm), without increasing the temperature and/or decreasing the pH value to acidic region (pH = 2–3) as is commonly employed in CWPO process for improved degradation efficiency. Full article

Biochar has demonstrated effectiveness in environmental remediation. However, the physicochemical properties of biochar change with natural aging, which potentially impacts its efficacy. This study was designed to evaluate the effects of aged biochar (at 1% and 5% rates) on the growth of Chinese cabbage, greenhouse gas emission, and Cd remediation in soils. Canada goldenrod (Solidago canadensis L.) feedstock biochar was subjected to three artificial aging processes (freeze–thaw cycle, dry–wet cycle, and hydrogen peroxide oxidation) to prepare aged biochar. Results showed that aging significantly altered properties and structure of biochar. Biochar addition had no effect on CH₄ emissions, but it decreased cumulative N₂O emission (all treatments) and increased cumulative CO₂ emission (only the pristine biochar at 5% application rate). Aged biochar showed no effect on microbial life strategy and Shannon index. However, PB-5% application shifted the life history strategies of A-strategists (resource acquisition microbe) towards Y-strategists (high-yield microbe) such as Proteobacteria, Gemmatimonadota, Bacteroidota, Firmicutes and Actinobacteriota, which partially attributed to the enhanced soil CO₂ emission. Aged biochar reduced plant uptake Cd and soil available Cd concentrations by up to 36.6% and 34.0%, respectively, ascribing to improved soil physicochemical properties and functional bacterial abundance. Full article

Nanopowders of hydroxyapatite (HA) and Fe-substituted hydroxyapatite (HAFe) were synthesized by wet precipitation on either MCM-41 (a synthetic, mesoporous aluminosilicate material) or an aluminum-containing MCM-41 (AlMCM) support. According to X-ray diffraction data, all of the synthesized materials are composite powders consisting of amorphous silicate and an HA phase with low crystallinity. The presence of aluminum and iron in the structure of the powders resulted in further amorphization. The obtained samples showed high specific surface areas (SSAs), ranging from 162.3 to 186.6 m²/g for MCM-41-HA and from 112.6 to 127.2 m²/g for AlMCM-HA. The hysteresis loops were found to be of type H3, indicating the formation of slit-like pores in the intercrystalline space, as confirmed by transmission electron microscopy, which revealed the presence of lamellar and flake-like particles. Catalytic activity tests showed that the conversion of dibenzothiophene depended on the iron concentration in the material and the acidity of the support. To further improve the catalytic activity of the materials, they were impregnated with molybdenum compounds. Active molybdenum peroxo complexes formed under these conditions enabled 100% conversion of dibenzothiophene. To our knowledge, this is the first study on the influence of MCM-41-HA- or AlMCM-HA-based materials on dibenzothiophene conversion via oxidative desulfurization using hydrogen peroxide as an oxidant. Full article

Microplastics (MPs) have been extensively studied in the marine environment, but reliable data on their sources and pathways in freshwater ecosystems, which are the main sources of such pollutants, are still limited. In this study, we investigated the spatiotemporal variations, characteristics, and sources of MPs in Nakivubo catchment, which drains waste and stormwater from Kampala city (Uganda) and empties it into Lake Victoria through the Nakivubo channel. Surface water samples (n = 117) were collected from thirteen sites in the Nakivubo catchment (S1 to S13) during the dry and wet seasons in 2022. The MPs were recovered by wet peroxide oxidation protocol, followed by salinity-based density separation, stereomicroscopy, and micro-attenuated total reflectance Fourier-transform infrared spectroscopy. All the samples had MPs, with mean concentrations ranging from 1568.6 ± 1473.8 particles/m³ during the dry season to 2140.4 ± 3670.1 particles/m³ in the wet season. Nakivubo catchment discharges an estimated 293.957 million particles/day into Lake Victoria. A Two-Way ANOVA revealed significant interactive effects of seasons and sampling sites on MPs abundance (p < 0.05). Spatially, the highest mean concentrations of MPs (5466.67 ± 6441.70 particles/m³) were in samples from site S3, which is characterized by poor solid waste and wastewater management practices. Filaments (79.7%) and fragments (17.9%) made of polyethylene (75.4%) and polyethylene/polypropylene co-polymer (16.0%) were the most common MPs. These are likely from single-use polyethylene and polypropylene packaging bags, water bottles, and filaments shed from textiles during washing. These results highlight the ubiquity of MPs in urban drainage systems feeding into Lake Victoria. To mitigate this pollution, urban authorities need to implement strict waste management policies to prevent plastic debris from entering drainage networks. Full article

Nitrophenols are persistent organic pollutants that pose serious environmental and health risks due to their toxic and lipophilic nature. Their persistence arises from strong aromatic stability and resistance to biodegradation, while their lipophilicity facilitates bioaccumulation, exacerbating ecological and human health concerns. To address this challenge, this study focuses on the synthesis and characterization of two different types of hybrid multi-core magnetic catalysts: (i) cobalt ferrite (Co-Fe₂O₄), which exhibits ferrimagnetic properties, and (ii) magnetite (Fe₃O₄), which demonstrates close superparamagnetic behavior and is coated with a novel and less hazardous phloroglucinol–glyoxal-derived resin. This approach aims to enhance catalytic efficiency while reducing the environmental impact, offering a sustainable solution for the degradation of nitrophenols in aqueous matrices. Transmission electron microscopy (TEM) images revealed the formation of a multi-core shell structure, with carbon layer sizes of 6.6 ± 0.7 nm for cobalt ferrite and 4.2 ± 0.2 nm for magnetite. The catalysts were designed to enhance the stability and performance in catalytic wet peroxide oxidation (CWPO) processes using sol–gel and solution combustion synthesis methods, respectively. In experiments of single-component degradation, the carbon-coated cobalt ferrite (CoFe@C) catalyst achieved 90% removal of 2-nitrophenol (2-NP) and 96% of 4-nitrophenol (4-NP), while carbon-coated magnetite (Fe₃O₄@C) demonstrated similar efficiency, with 86% removal of 2-NP and 94% of 4-NP. In the multi-component system, CoFe@C exhibited the highest catalytic activity, reaching 96% removal of 2-NP, 99% of 4-NP, and 91% decomposition of H₂O₂. No leaching of iron was detected in the coated catalysts, whereas the uncoated materials exhibited similar and significant leaching (CoFe: 5.66 mg/L, Fe₃O₄: 12 mg/L) in the single- and multi-component system. This study underscores the potential of hybrid magnetic catalysts for sustainable environmental remediation, demonstrating a dual-function mechanism that enhances catalytic activity and structural stability. Full article

In recent years, efforts have been made in developing new and more efficient water purification methods and the synthesis of catalysts with greater catalytic activity that are more stable and can be used in wide pH ranges. Pillared clays represent a viable alternative for removing organic contaminants. The clays, usually smectites, are modified by inserting inorganic pillars (Al, Zr, Cr, Fe, Ti, Ga, and Mn) between the layers of the clay, increasing its surface area, porosity, catalytic activity, and thermal stability. This review describes the importance of using pillared clays with different polyoxycations in Fenton, photo-Fenton, ozonation, wet catalytic oxidation of hydrogen peroxide, and photocatalysis processes. Pillared iron clays (Fe-PILCs) are promising catalysts capable of generating hydroxyl radicals that can oxidize organic contaminants, thus facilitating their removal. The current challenges of the PILC application at industrial scale are also discussed. Full article

Zinc-substituted cobalt ferrites were obtained by a green method using a black grape extract as a reductant and fuel. XRD analysis confirmed the spinel structure of the synthesized ferrites. An increase in the lattice constant is explained by increased Zn content. SEM analysis confirmed changes in surface morphology, whereas FTIR spectra demonstrated the presence of organic species in the samples, which originated from grape extract. The content of Co(II) ions in octahedral sites as a function of the ratio between Fe(III) ions in A- and B-sites was calculated from Mössbauer data. pH_PZC rose from 7.85 to 8.13 with an increase in zinc content, indicating a positive charge of the adsorbent surface at natural pH. The adsorption–catalytic properties of the spinel samples were investigated in terms of Congo Red (CR) dye removal. The mechanism of CR adsorption on the ferrite surface includes electrostatic and donor–acceptor interactions with the adsorbent surface. Furthermore, the sample with x(Zn) = 0.4 exhibited the highest degradation rate constant k = 0.102 min⁻¹ in the peroxide oxidation of CR, whereas the sample with x(Zn) = 1.0 exhibited the highest adsorption capacity. The electron transfer between ferrite samples and hydrogen peroxide was evidenced using electrochemical tests. The green-synthesized Co-Zn ferrites demonstrate a big potential as adsorbents/catalysts for water treatment. Full article

The single-atom catalyst (SAC) activated persulfate process has emerged as a highly efficient technology for eliminating refractory organic compounds in aqueous environments. This review delves into the intricacies of utilizing SACs for the effective removal of various contaminants in water. The common supports and the preparation procedures of SACs are summarized at first. The synthesis methods of SACs (i.e., wet chemical method, one-pot hydrothermal method, and high-temperature pyrolysis method) are also described. Then, a comprehensive overview of the diverse reaction mechanisms in SAC-activated persulfate systems is presented, including a radical oxidation process via sulfate or hydroxyl radicals and superoxide radicals, or a nonradical process via single oxygen, surface active complex, and high-valent metal-oxo species oxidation. The impact of key factors such as peroxides concentration, SAC dosage, reaction pH, inorganic anions, organic matter, operando stability, and real water is also delved. The removal of various pollutants (i.e., azo dyes, phenolic compounds, pharmaceuticals, and bacteria) by this process is further summarized. Finally, the challenges and perspectives in the field of water treatment utilizing SACs are discussed. Full article

In order to explore the possibilities of increasing the hydrophilicity of carbon-based adsorbents, catalysts, or electrode materials in aqueous solutions, the oxidation of wood-based activated biochar using H₂O₂ was investigated. The properties of oxidized activated biochar obtained at different activation temperatures (600, 700, and 800 °C) and H₂O₂ oxidized for 15–180 min were investigated using the characteristics of surface functionality, elemental composition, porous structure, contact angle measurements, FTIR spectroscopy, and immersion calorimetry. It was observed that the optimal oxidation time was different for each sample depending on activation temperature, and the degree of oxidation can be tailored by changing the oxidation time. The course of oxidation depends on the degree of graphitization and functionalization, determined by the activation temperature. It was established that the highest degree of oxidation and increase in wettability is observed for samples with the lowest degree of activation obtained at a temperature of 600 °C. Full article

Soybean meal (SM) adhesive is widely acknowledged as a viable substitute for traditional formaldehyde-based adhesives, given its ability to be easily modified, the utilization of renewable sources, and its eco-friendly characteristics. However, the application of SM adhesive in manufacturing has been impeded due to its restricted bonding capacity and inadequate water resistance. Researchers in the wood industry have recognized the significance of creating an SM-based adhesive, which possesses remarkable adhesive strength and resistance to water. This study endeavors to tackle the issue of inadequate water resistance in SM adhesives. Sodium lignosulfonate (L) was oxidized using hydrogen peroxide (HP) to oxidized lignin (OL) with a quinone structure. OL was then used as a modifier, being blended with SM to prepare SM-based biomass (OLS) adhesives with good water resistance, which was found practically through its utilization in the production of plywood. The influence of the HP dosage and OL addition on plywood properties was examined. The changes in the lignin structure before and after oxidation were confirmed using gel permeation chromatography (GPC), Fourier transform infrared spectroscopy (FT-IR), and X-ray photoelectron spectroscopy (XPS). The curing behavior and thermal stability of OLS adhesives were analyzed using dynamic mechanical analysis (DMA) and thermogravimetric (TG) analysis. The reaction mechanism was also investigated using FT-IR and XPS. The outcomes indicated a decrease in the molecular weight of L after oxidation using HP, and, at the same time, quinone and aldehyde functionalized structures were produced. As a result of the reaction between the quinone and aldehyde groups in OL with the amino groups in SM, a dense network structure formed, enhancing the water resistance of the adhesive significantly. The adhesive displayed exceptional resistance to water when the HP dosage was set at 10% of L and the OL addition was 10% based on the mass of SM. These specific conditions led to a notable enhancement in the wet bonding strength (63 °C, 3 h) of the plywood prepared using the adhesive, reaching 0.88 ± 0.14 MPa. This value represents a remarkable 125.6% increase when compared to the pure SM adhesive (0.39 ± 0.02 MPa). The findings from this study introduce a novel approach for developing adhesives that exhibit exceptional water resistance. Full article

In the food industry, including the fat and oil sector, chemical methods are commonly used for routine quality analyses. These analyses are typically time-consuming and often require the use of toxic solvents and reagents. Moreover, in some cases, sophisticated instruments such as gas chromatographs are used, which are expensive and a form of advanced instrumentation. As an alternative approach, it is possible to use simpler methods utilizing spectroscopic techniques, like FTIR spectroscopy, the results of which have been reported to correlate with those obtained using wet chemical methods. In this study, we used the FTIR technique to assess the oxidative stability of some edible oils available on the Polish market. The oils studied were nigella seed, pumpkin seed, flax seed, linseed, evening primrose seed, and thistle seed oils. FTIR/ATR spectra of the undiluted oils were recorded in the range of 500–4000 cm⁻¹ with a resolution of 2 cm⁻¹. To monitor the oxidation process, the peak at 721 cm⁻¹, related to cis double bonds of unsaturated fatty acids (UFAs), and the peak intensity at 986 cm⁻¹, associated with the presence of conjugated diene groups of hydroperoxides (HPs), were analyzed. The content of free fatty acids (FFAs) and the ratio of unsaturated/saturated fatty acids (UFAs/SFAs) were qualitatively expressed by the intensity band at 1712 cm⁻¹ and the peak ratio of 3011/2925 cm⁻¹, respectively. Additionally, using the Triphenylphosphine/Triphenylphosphine Oxide (TPP/TPPO) assay, the peroxide value (PV) was calculated. The parameter analysis revealed significant variations among the tested oils. Moreover, all determined parameters from the FTIR spectrum changed during the oxidation process. However, the nature and degree of these changes differed depending on the oil tested. The findings indicated that the straightforward instrumental FTIR method could serve as a rapid analytical tool for evaluating the level of oxidation or comparing the quality of edible oils. Full article

In this study, we investigated the catalytic properties of mono- and bimetallic palladium (Pd) and platinum (Pt) nanoparticles deposited via supercritical fluid reactive deposition (SFRD) on titanium dioxide (TiO₂) powder. Transmission electron microscopy analyses verified that SFRD experiments performed at 353 K and 15.6 MPa enabled the deposition of uniform mono- and bimetallic nanoparticles smaller than 3 nm on TiO₂. Electron-dispersive X-ray spectroscopy demonstrated the formation of alloy-type structures for the bimetallic PdPt nanoparticles. H₂O₂ is an excellent oxidizing reagent for the production of fine and bulk chemicals. However, until today, the design and preparation of catalysts with high H₂O₂ selectivity and productivity remain a great challenge. The focus of this study was on answering the questions of (a) whether the catalysts produced are suitable for the direct synthesis of hydrogen peroxide (H₂O₂) in the liquid phase and (b) how the metal type affects the catalytic properties. It was found that the metal type (Pd or Pt) influenced the catalytic performance strongly; the mean productivity of the mono- and bimetallic catalysts decreased in the following order: Pd > PdPt > Pt. Furthermore, all catalysts prepared by SFRD showed a significantly higher mean productivity compared to the catalyst prepared by incipient wetness impregnation. Full article

It is very important to choose a suitable method and catalyst to treat coking wastewater. In this study, Fe–Ce–Al/MMT catalysts with different Fe/Ce molar ratios were prepared, characterized by XRD, SEM, and N₂ adsorption/desorption, and treated with coking wastewater. The results showed that the optimal Fe–Ce–Al/MMT catalyst with a molar ratio of Fe/Ce of 7/3 has larger interlayer spacing, specific surface area, and pore volume. Based on the composition analysis of real coking wastewater and the study of phenol simulated wastewater, the response surface test of the best catalyst for real coking wastewater was carried out, and the results are as follows: initial pH 3.46, H₂O₂ dosage 19.02 mL/L, Fe²⁺ dosage 5475.39 mL/L, reaction temperature 60 °C, and reaction time 248.14 min. Under these conditions, the COD removal rate was 86.23%. Full article

Quinoline (QN) is highly toxic and carcinogenic and has been detected in soil, groundwater, and biological tissues. Advanced oxidation processes (AOPs) have shown promise to address its degradation in wastewater treatment, with catalytic wet peroxide oxidation (CWPO) being highlighted due to its cost-effectiveness and mild operation. However, developing active and inexpensive catalysts is crucial for CWPO’s effectiveness. Another pressing issue is the accumulation of mixed, dirty plastic solid waste (PSW), particularly polyolefins used in packaging. Although recycling rates have increased, much plastic packaging remains in landfills. However, polyolefins can be converted into carbon-based nanostructured materials (CNMs), such as carbon nanotubes (CNTs), through chemical vapor deposition (CVD) using PSW as a carbon precursor. While many studies focus on CNT preparation, their application is often overlooked. In this context, this work proposes the preparation of CNMs, particularly CNTs, through CVD using a single-stage pyrolysis reactor. Polyolefins (LDPE, HDPE, and PP), both individually and in a mixture simulating PSW, were used as carbon sources. Given a sufficiently high temperature, the desired CNT architecture was successfully synthesized regardless of the starting polymer. These CNMs were then tested as catalysts for CWPO in simulated wastewater containing QN. The results showed a rapid degradation of QN (30–120 min) and high removals of total organic carbon (TOC) and aromatic compounds (75% and >90%, respectively), demonstrating the applicability of PSW-derived CNTs in the CWPO process for QN abatement. Full article

A subcritical water degradation and extraction method was developed to remediate environmental soils contaminated by highly recalcitrant organochlorine pollutants. Hydrogen peroxide was used to effectively decompose organochlorine pollutants under subcritical water conditions. As a method optimization study, the static wet oxidation of chlorophenols was first performed in subcritical water with and without added hydrogen peroxide. Complete oxidation was achieved using an added oxidant, and thus, the oxidation and extraction of chlorophenols from a sand matrix was then attempted. Complete oxidation and extraction with added oxidant were achieved within 30 min at 100 °C. We then investigated the subcritical water degradation and extraction of dieldrin, mirex, and p,p′-DDD. These organochlorine pesticides were not as easily oxidized as the chlorophenols, and the benefit of adding hydrogen peroxide was only clearly observed at 200 °C. Approximately a 20% increase in degradation was noted for each pesticide and insecticide at this temperature. Unfortunately, this difference was not observed with an increase in temperature to 250 °C, except in some cases, where the amount of degradation byproducts was reduced. Dieldrin and p,p′-DDD were essentially destroyed at 250 °C, while all the pesticides and the insecticides were completely removed from the sand at this temperature. The proposed method was then used to remediate a soil sample highly contaminated with DDT. The soil was obtained from the grounds of an old DDT mixing facility in Virginia and has been aging for several decades. Not only was 100% removal of DDT from this soil achieved using the proposed method at 250 °C, but also, the extracted DDT was completely destroyed during the process. The proposed remediation method, therefore, demonstrates a high potential as an efficient and environmentally sound technique for the detoxification of soils. Full article