Search Results (693)

This work demonstrates the potential of polydimethylsiloxane sponges for removing organic UV filter compounds such as octinoxate from aqueous solutions. The sponges were fabricated using simple templates made of hydrophilic fused or pressed particles (sugar or NaCl salt) with an approximate particle size of 0.4 mm. Among the prepared sponges, those templated with sugar cubes or coarse salt exhibited the highest adsorption capacity, effectively adsorbing up to 0.6% of their own mass in octinoxate. The PDMS sponges were fully regenerable, allowing for the complete removal of octinoxate without any detectable changes in their adsorption properties or dry weight. Due to their simple fabrication, ease of handling, ability to float, and reusability, PDMS sponges present an environmentally friendly and low-maintenance alternative to conventional filtration systems for the removal of octinoxate and potentially other UV filter compounds from environmental surface waters and recreational water bodies. Full article

Due to the complex mineral composition, low clay content, and strong heterogeneity of the mixed sedimentary shale in the Xinjiang Salt Lake Basin, the wettability characteristics of the reservoir and their influencing factors are not yet clear, which restricts the evaluation of oil-bearing properties and the identification of sweet spots. This paper analyzed mixed sedimentary shale samples from the Lucaogou Formation of the Jimsar Sag and the Fengcheng Formation of the Mahu Sag. Methods such as petrographic thin sections, X-ray diffraction, organic matter content analysis, and argon ion polishing scanning electron microscopy were used to examine the lithological and mineralogical characteristics, geochemical characteristics, and pore space characteristics of the mixed sedimentary shale reservoir. Alternating imbibition and nuclear magnetic resonance were employed to quantitatively characterize the wettability of the reservoir and to discuss the effects of compositional factors, lamina types, and pore structure on wettability. Research findings indicate that the total porosity, measured by the alternate imbibition method, reached 72% of the core porosity volume, confirming the effectiveness of alternate imbibition in filling open pores. The Lucaogou Formation exhibits moderate to strong oil-wet wettability, with oil-wet pores predominating and well-developed storage spaces; the Fengcheng Formation has a wide range of wettability, with a higher proportion of mixed-wet pores, strong heterogeneity, and weaker oil-wet properties compared to the Lucaogou Formation. TOC content has a two-segment relationship with wettability, where oil-wet properties increase with TOC content at low TOC levels, while at high TOC levels, the influence of minerals such as carbonates dominates; carbonate content shows an “L” type response to wettability, enhancing oil-wet properties at low levels (<20%), but reducing it due to the continuous weakening effect of minerals when excessive. Lamina types in the Fengcheng Formation significantly affect wettability differentiation, with carbonate-shale laminae dominating oil pores, siliceous laminae contributing to water pores, and carbonate–feldspathic laminae forming mixed pores; the Lucaogou Formation lacks significant laminae, and wettability is controlled by the synergistic effects of minerals, organic matter, and pore structure. Increased porosity strengthens oil-wet properties, with micropores promoting oil adsorption through their high specific surface area, while macropores dominate in terms of storage capacity. Wettability is the result of the synergistic effects of multiple factors, including TOC, minerals, lamina types, and pore structure. Based on the characteristic that oil-wet pores account for up to 74% in shale reservoirs (mixed-wet 12%, water-wet 14%), a wettability-targeted regulation strategy is implemented during actual shale development. Surfactants are used to modify oil-wet pores, while the natural state of water-wet and mixed-wet pores is maintained to avoid interference and preserve spontaneous imbibition advantages. The soaking period is thus compressed from 30 days to 3–5 days, thereby enhancing matrix displacement efficiency. Full article

The use of chloride-based deicing salts, particularly sodium chloride (NaCl) and calcium chloride (CaCl₂), is a common practice in cold regions for maintaining road safety during winter. However, the accumulation of salt residues in adjacent soils poses serious environmental threats, including reduced pH, increased electrical conductivity (EC), disrupted soil structure, and plant growth inhibition. This study aimed to evaluate the combined effect of activated carbon (AC) and Pennisetum alopecuroides, a salt-tolerant perennial grass, in alleviating salinity stress under deicer-treated soils. A factorial greenhouse experiment was conducted using three fixed factors: (i) presence or absence of Pennisetum alopecuroides, (ii) deicer type (NaCl or CaCl₂), and (iii) activated carbon mixing ratio (0, 1, 2, 5, and 10%). Soil pH, EC, and ion concentrations (Na⁺, Cl⁻, Ca²⁺) were measured, along with six plant growth indicators. The results showed that increasing AC concentrations significantly increased pH and reduced EC and ion accumulation, with the 5% AC treatment being optimal in both deicer systems. Plant physiological responses were improved in AC-amended soils, especially under CaCl₂ treatment, indicating less ion toxicity and better root zone conditions. The interaction effects between AC, deicer type, and plant presence were statistically significant (p < 0.05), supporting a synergistic remediation mechanism involving both adsorption and biological uptake. Despite the limitations of short-term controlled conditions, this study offers a promising phytomanagement strategy using natural adsorbents and salt-tolerant plants for sustainable remediation of salt-affected soils in road-adjacent and urban environments. 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

This study investigates the use of a salt template to synthesize mesoporous bioactive glass (MBG). Different salts were used as hard templates to create pores in the glass structure to investigate the possibility of using acid-soluble salt templates and to understand the properties of glass synthesized without thermal treatment. The MBGs were synthesized in a TRIS buffer solution at a pH of 9.5 to allow hydrolysis of the metal oxide precursors. The glass was then washed with mild acid to remove the template. After the samples were washed, some were subjected to thermal treatment, while others were not to investigate the impact of thermal treatment on the structure of the MBG. The successful synthesis of MBG was confirmed by X-ray diffraction, Fourier-transfer infrared spectroscopy, scanning emission scanning microscope, and nitrogen adsorption–desorption analysis. This synthesized MBG had a large surface area, pore volume, pore size, and high drug loading efficiency. MBG synthesized without thermal treatment had slower degradation over the test period, but higher loading efficiency and slower drug release, making it appropriate for applications requiring long-term drug delivery while maintaining its bioactivity. Full article

The separation of particles smaller than 1 µm either by composition or by size is still a challenge. For the separation of SiO₂ and SnO₂, the creation of a selective separation feature and the specific adsorption of salts and surfactants were investigated. The adsorption of various salts, e.g., AlCl₃, ZnCl₂, MnCl₂ and MgCl₂ were therefore analyzed, and the necessary concentration for the charge reversal of the material was determined. It was noticed that the investigated materials differ in their isoelectric point (IEP) and therefore in their adsorption behavior because only ZnCl₂ and MgCl₂ are suitable for a charge reversal of both metal oxides. The phase transfer of the pure material at different pH values with ZnCl₂ or MgCl₂ and sodium dodecyl sulfate (SDS) revealed that the adsorption behavior of the particle has an influence on the phase transfer. As a result, the phase transfer of SiO₂ is pH dependent, whereas the phase transfer of SnO₂ operates over a wider pH range. This allowed the separation of SiO₂ and SnO₂ to be controlled by the salt and surfactant concentration as well as pH. The separation of SiO₂ and SnO₂ was investigated for various parameters such as salt and surfactant concentration, particle concentration and composition of the mixture. Also, pH 8, where a selective phase transfer for SiO₂ occurs, and pH 6, where the greatest difference between the materials exists, were also investigated. By comparing the parameters, it was found that the combination of ZnCl₂/SDS and MgCl₂/SDS enables a selective separation of the materials. Furthermore, it was also found that the concentration of SDS has a significant effect on the separation, as the formation of a bilayer structure is important for the separation, and therefore, higher SDS concentrations are required at higher particle concentrations to increase the separation efficiency. Full article

This study presents a sustainable approach for synthesizing high-performance activated carbon from Spirulina Alga through hydrothermal carbonization followed by chemical activation using potassium hydroxide. The resulting activated carbon exhibited a high Brunauer–Emmett–Teller (BET) surface area of 1747 m²/g and a total pore volume of 1.147 cm³/g, with micropore volume accounting for 0.4 cm³/g. Characterization using Scanning Electron Microscopy-Energy Dispersive X-ray Spectroscopy (SEM-EDS), X-ray Photoelectron Spectroscopy (XPS), and gas adsorption analyses confirmed the presence of hierarchical micro- and mesoporosity as well as favorable surface functional groups. The synthesized carbon was used to fabricate electrodes for membrane capacitive deionization (MCDI) along with cation and anion-selective membranes, which were then tested with saline water (500–5000 ppm) and synthetic hard water (898 ppm of total salts). The salt adsorption capacity (SAC) reached 25 (batch) to 40 (continuous) mg/g, while rapid adsorption rates with average salt adsorption rates (ASARs) values exceeding 10 (batch) to 30 (continuous) mg·g⁻¹·min⁻¹ during early stages were obtained. Batch MCDI experiments demonstrated a higher SAC compared to continuous operation, with non-monotonic trends in SAC observed as a function of feed concentration. Ion adsorption kinetics were influenced by ion valency, membrane selectivity, and pore structure. The specific energy consumption (SEC) was calculated as 8–21 kJ/mol for batch and 0.1–0.5 kJ/mol for continuous process. These performance metrics are on par with or surpass those reported in the recent literature for similar single-electrode CDI configurations. The results demonstrate the viability of using Alga-derived carbon as an efficient and eco-friendly electrode material for water desalination technologies. Full article

This study explores the utilization of waste grape pomace-derived hydrochar as an efficient adsorbent for lead (Pb²⁺) removal from aqueous solutions. Hydrochar was produced via hydrothermal carbonization (HTC) at 220 °C, followed by doping with magnesium and iron salts, and subsequent pyrolysis at 300 °C to obtain Fe/Mg-pyro-hydrochar (FeMg-PHC). The material’s structural and morphological changes after Pb²⁺ adsorption were examined using FTIR. FTIR revealed chemisorption and ion exchange as key mechanisms, shown by decreased hydroxyl, carbonyl, and metal–oxygen peaks after Pb²⁺ adsorption. Adsorption tests under varying pH, contact time, and initial Pb²⁺ concentrations revealed optimal removal at pH 5. Kinetic modeling indicated that the process follows a pseudo-second-order model, suggesting chemisorption as the dominant mechanism. Isotherm analysis showed that the Sips model best describes the equilibrium, with a maximum theoretical adsorption capacity of 157.24 mg/g. Overall, the simple two-step synthesis—HTC followed by pyrolysis—combined with metal doping yields a highly effective and sustainable adsorbent for Pb²⁺ ion removal from wastewater. Full article

The aim of this work was to investigate the influence of ionic strength and temperature on the adsorption of Reactive Black 5 dye on commercial powdered activated carbon. Adsorption experiments were performed at 45 °C with the addition of NaCl (c₀ = 0.01, 0.05, 0.10 and 1.00 M) and Na₂SO₄ (c₀ = 0.01 M). The results were compared with those obtained for both salts (c₀ = 0.01 M) at three additional temperatures: 25, 35 and 55 °C. For all adsorption experiments, kinetic and thermodynamic studies were performed. This research showed that the addition of NaCl, even in the concentration of only c₀ = 0.01 M, significantly enhanced dye adsorption and that higher NaCl concentration resulted in higher adsorption capacity. In addition, slightly higher adsorption was observed when Na₂SO₄ was added to the dye solution at the same concentration as NaCl, as well as at a higher temperature, regardless of the salt added to the dye solution. It was also shown that adsorption is kinetically controlled, assuming a pseudo-second-order model, and that intraparticle diffusion is not the only process that influences the adsorption rate. Finally, calculated thermodynamic parameter values for both salts (c₀ = 0.01 M) indicate that adsorption was a spontaneous endothermic process. Full article

To overcome the low efficiency, high cost and less environmentally friendly limitations in existing textile wastewater disposal technology, an innovative approach of cation exchange membrane electrolysis coupled with magnesium salt precipitation (CEM-MSP) was implemented. This method simultaneously achieved the high-efficiency adsorption decolorization of dyes and the recovery of lye. The results indicated that cation exchange membrane electrolysis with MgSO₄ added to the anode chamber (CEM-EA) exhibited excellent decolorization performance on DB86 dye and achieved low residual Mg²⁺ concentration. Furthermore, the adsorption mechanism of Mg(OH)₂ on DB86 was systematically investigated. The adsorption process fitted with the first-order kinetic, where the adsorption of DB86 by Mg(OH)₂ was dominated by electrostatic attraction. Detailed comparison of the four systems demonstrated that CEM-EA was superior to the single magnesium addition method (85.24%) or the stand-alone membrane electrolysis method (10.36%), with 99% decolorization efficiency. In comparison to the cation exchange membrane electrolysis with MgSO₄ added to the cathode chamber (CEM-EC), the CEM-EA could diminish the Mg²⁺ concentration in the effluent to facilitate the lye recovery while guaranteeing the decolorization efficiency. In addition, the DB86 adsorption behavior during the formation of Mg(OH)₂ in the cathode chamber was investigated. The Mg(OH)₂ particles were relatively dense copper-blue agglomerates with a thin lamellar layer on the surface. Notably, only slight mass contamination was observed on the cation exchange membrane (CEM) surface after multiple cycles. Minor CEM contamination illustrated the stable treatment efficiency of the CEM-EA after several cycles. This study constructed a novel approach integrating membrane electrolysis with magnesium salt precipitation, delivering valuable technical solutions for textile wastewater disposal. Full article

Elevated phosphorus levels in aquatic ecosystems have been identified as a critical driver of eutrophication processes, necessitating resource-recovery remediation strategies. Adsorption techniques show particular promise for nutrient recovery due to their selective binding capacities and operational feasibility. In this study, the Mg- and Ca-modified biogas residue-based biochar (Ca-Mg/BC) was successfully prepared via a “bimetallic loading-pyrolysis” modification strategy. The optimum temperature for the calcination of the material and the salt solution impregnation concentrations were determined experimentally through optimization of the synthesis conditions. Structural and chemical analyses of Ca–Mg/BC demonstrated that the material contains MgO and CaO. The specific surface area of Ca–Mg/BC was 8.49 times higher than that of the unmodified biochar (BC). The optimized Ca–Mg/BC achieved 95% phosphate removal rate (157.13 mg/g adsorption capacity). FTIR and XPS characterization results indicated the importance of Ca/Mg loading in phosphate capture. MgO and CaO were mainly loaded on the surface of the material and adsorbed phosphate through a chemical reaction. Crucially, the phosphate-laden biochar exhibited potential as a nutrient-enriched soil amendment, opening the material loop from wastewater treatment to agricultural applications. This sustainable strategy simultaneously addresses water pollution control and sustainable development, providing environmentally benign solutions compatible with industrial effluent treatment and sustainable agriculture practices. Full article

This study investigated soil salinization processes in the Pavlodar region of Kazakhstan by comparing key soil parameters—namely, electrical conductivity (EC), pH, exchangeable sodium percentage (ESP), and sodium adsorption ratio (SAR) under irrigated and non-irrigated conditions across different agro-climatic zones and soil types (Haplic Chernozems, Haplic Kastanozems). The focus was on understanding the effects of irrigation and natural factors on soil salinization. Statistical analysis, including descriptive statistics and significance testing, was employed to evaluate differences between soil types, locations, and management practices. The research revealed secondary salinization (EC > 2 dS/m, ESP > 15%) in the topsoil of irrigated Haplic Kastanozems soils in the central Aksu district. This degradation was markedly higher than in non-irrigated plots or irrigated Haplic Chernozems in the northern Irtysh district, highlighting the high vulnerability of Haplic Kastanozems soils under current irrigation management given Aksu’s climatic conditions, which are characterized by high evaporative demand (driven by summer temperatures) and specific precipitation patterns that contribute to soil moisture deficits without irrigation. While ESP indicated sodicity, SAR values remained low. Natural factors, including potentially saline parent materials and likely shallow groundwater dynamics influenced by irrigation, appear to contribute to the observed patterns. The findings underscore the need for implementing optimized irrigation and drainage management, particularly in the Aksu district, potentially including water-saving techniques (e.g., drip irrigation) and selection of salt/sodicity-tolerant crops. A comprehensive approach integrating improved water management, agronomic practices, and potentially soil amendments is crucial for mitigating soil degradation and ensuring sustainable agriculture in the Pavlodar region. Further investigation including groundwater monitoring is recommended. Full article

To address the disposal challenges of waste SCR catalysts and the urgent need for sustainable solutions in heavy metal pollution control, this study proposes a green resource utilization strategy based on the sub-molten salt method to convert waste SCR catalysts into highly efficient lead ion adsorbents. Titanate-based adsorbent materials with a loose porous structure were successfully prepared by optimizing the process parameters (reaction temperature of 160 °C, NaOH concentration of 70%, and reaction time of 2 h). The experiments showed that the adsorption efficiency was as high as 99.65% and the maximum adsorption capacity was 76.08 mg/g under ambient conditions (adsorbent dosage of 1.2 g/L, initial Pb(II) concentration of 100 mg/L, contact time of 60 min, and pH = 4). Kinetic analysis showed that the quasi-second-order kinetic model (R² = 0.9985) could better describe the adsorption process, indicating chemisorption as the dominant mechanism. Characterization analysis confirmed that subsequent to the adsorption process, Pb₃(CO₃)₂(OH)₂ formed on the surface of the adsorbent material is the adsorption product of Pb(II) and C-O through ion exchange and surface complexation. This study transforms waste SCR catalysts into sustainable titanate adsorbents through a low-energy green process, providing an eco-efficient solution for heavy metal wastewater treatment while aligning with circular economy principles and sustainable industrial practices. Full article

To address the technical challenge of high polymer gel viscosity reducers losing viscosity at elevated temperatures and difficulty in controlling fluid loss, a polymer-based nano calcium carbonate composite high-temperature tackifier named GW-VIS was prepared using acrylamide (AM), 2-acrylamido-2-methylpropanesulfonic acid (AMPS), N-vinylpyrrolidone (NVP), and nano calcium carbonate as raw materials through water suspension polymerization. This polymer gel can absorb water well at room temperature and has a small solubility. After a long period of high-temperature treatment, most of it can dissolve in water, increasing the viscosity of the suspension. The structure of the samples was characterized by infrared spectroscopy, thermogravimetric analysis, and scanning electron microscopy, and their performance was evaluated. Rheological tests indicated that the 0.5% water suspension had a consistency coefficient (k = 761) significantly higher than the requirement for clay-free drilling fluids (k > 200). In thermal resistance experiments, the material maintained stable viscosity at 180 °C (reduction rate of 0%), and only decreased by 14.8% at 200 °C. Salt tolerance tests found that the viscosity reduction after hot rolling at 200 °C was only 17.31% when the NaCl concentration reached saturation. Field trials in three wells in the Liaohe oilfield verified that the clay-free drilling fluid supported formation operations successfully. The study shows that the polymer gel has the potential to maintain rheological stability at high temperatures by forming a network structure through polymer chain adsorption and entanglement, with a maximum temperature resistance of up to 200 °C, providing an efficient drilling fluid for deep oil and gas well development. It is feasible to select nano calcium carbonate to participate in the research of high-temperature resistant polymer materials. Meanwhile, the combined effect of monomers with large steric hindrance and inorganic materials can enhance the product’s temperature resistance and resistance to NaCl pollution. Full article

The rapid pace of industrialization has led to widespread heavy metal contamination in water and soil, highlighting the need for efficient remediation strategies. Among various approaches, adsorption has proven to be an effective method for treating contaminated environments. Layered double hydroxide (LDH) is frequently used in such applications. However, its adsorption efficiency remains limited. In this study, glutamic acid diacetate tetrasodium salt (GLDA) was incorporated into ZnAl LDH via a straightforward co-precipitation and ion exchange method, yielding a modified material, GLDA-LDH, which was subsequently applied for the adsorption of Pb(II) and Cd(II). Adsorption behavior was investigated through kinetic and isothermal models, with results indicating that the process followed pseudo-second-order kinetics and fit well with the Langmuir isotherm, suggesting chemisorption onto monolayer surface. The maximum adsorption capacities reached 219.2 mg/g for Pb(II) and 121.9 mg/g for Cd(II). Furthermore, GLDA-LDH exhibited a strong retention capability for metal ions with minimal desorption and remained effective in the presence of hard water and contaminated soils. XPS analysis revealed distinct interaction mechanisms; surface oxygen and carboxyl groups played a key role in Pb(II) adsorption, whereas nitrogen coordination was involved in Cd(II) uptake. These results point to the potential of GLDA-LDH as a reliable material for addressing heavy metal pollution and provide insights into the design of enhanced LDH-based adsorbents. Full article