RESUMEN

During the water treatment process, chlorination and ultraviolet (UV) sterilization can modify microplastics (MPs) and alter their physicochemical properties, causing various changes between MPs and other pollutants. In this study, the impact of chlorination and UV modification on the physicochemical properties of polystyrene (PS) and polyvinyl chloride (PVC) were investigated, and the adsorption behavior of pefloxacin (PEF) before and after modification was examined. The effect of pH, ionic strength, dissolved organic matter, heavy metal ions and other water environmental conditions on adsorption behavior was revealed. The results showed that PS had a higher adsorption capacity of PEF than PVC, and the modification increased the presence of O-containing functional groups in the MPs, thereby enhancing the adsorption capacity of both materials. Chlorination had a more significant impact on the physicochemical properties of MPs compared to UV irradiation within the same time period, leading to better adsorption performance of chlorination. The optimal pH for adsorption was found to be 6, and NaCl, sodium alginate and Cu2+ would inhibit adsorption to varying degrees, among which the inhibition caused by pH was the strongest. Chlorination and UV modification would weaken the inhibitory effect of environmental factors on the adsorption of PEF by MPs. The main mechanisms of adsorption involved electrostatic interaction and hydrogen bonding. The study clarified the effects of modification on the physicochemical properties of MPs, providing reference for subsequent biotoxicity analysis and environmental protection studies.

Asunto(s)

RESUMEN

Electrochemical upcycling of end-of-life polyethylene terephthalate (PET) using renewable electricity offers a route to generate valuable chemicals while processing plastic wastes. However, it remains a huge challenge to design an electrocatalyst with reliable structure-property relationships for PET valorization. Herein, spinel Co3O4 with rich oxygen vacancies for improved activity toward formic acid (FA) production from PET hydrolysate is reported. Experimental investigations combined with theoretical calculations reveal that incorporation of VO into Co3O4 not only promotes the generation of reactive hydroxyl species (OH*) species at adjacent tetrahedral Co2+ (Co2+ Td), but also induces an electronic structure transition from octahedral Co3+ (Co3+ Oh) to octahedral Co2+ (Co2+ Oh), which typically functions as highly-active catalytic sites for ethylene glycol (EG) chemisorption. Moreover, the enlarged Co-O covalency induced by VO facilitates the electron transfer from EG* to OH* via Co2+ Oh-O-Co2+ Td interaction and the following C─C bond cleavage via direct oxidation with a glyoxal intermediate pathway. As a result, the VO-Co3O4 catalyst exhibits a high half-cell activity for EG oxidation, with a Faradaic efficiency (91%) and productivity (1.02 mmol cm-2 h-1) of FA. Lastly, it is demonstrated that hundred gram-scale formate crystals can be produced from the real-world PET bottles via two-electrode electroreforming, with a yield of 82%.

RESUMEN

In this work, a kind of novel Chitosan (Cs)-doped zeolite imidazole framework (ZIF-8@Cs) with a larger surface area and a smaller pore size was synthesised via a facial solvothermal approach and applied to remove Cu2+ from mine wastewater. Compared to nondoped ZIF-8, ZIF-8@Cs exhibited a stronger adsorption performance and removal efficiency. The reason was that ZIF-8@Cs doped by the Cs could suppress the aggregation and increase the monodispersity of ZIF-8. Using the high-performance ZIF-8@Cs, as a novel adsorbent, was successfully developed for the efficient removal of Cu2+ from mine wastewater. Various parameters, such as contact time, initial Cu2+ concentration, adsorbent dosage, and pH, were investigated. The results showed that a removal efficiency of 85% was obtained at 4 h contact time for a Cu2+ concentration of 30 mg/L at the optimum pH of 6.0. Equilibrium data were analysed using different isothermal models and kinetic models, analytic results indicated that the capture of Cu2+ by ZIF-8@Cs could favourably comply with the pseudo-first-order kinetic model and Langmuir isotherm model. The single-layer adsorption of Cu2+ on ZIF-8@Cs was dominated by diffusional mass transfer. Additionally, the results of the thermodynamic analysis indicated that the adsorption of Cu2+ by ZIF-8/Cs was a spontaneous, exothermic, and ordered process. Overall, the results reported herein indicated that ZIF-8/Cs with high adsorption efficiency are very attractive and imply a potential practical application for the removal of potentially toxic elements in wastewater.

RESUMEN

HYPOTHESIS: Host rock weathering and incipient pedogenesis result in the exposition of minerals, e.g., clay minerals in sedimentary limestones. Once exposed, these minerals provide the surfaces for fluid-solid interactions that control the fate of dissolved or suspended compounds such as organic matter and colloids. However, the functional and compositional diversity of organic matter and colloids limits the assessment of reactivity and availability of clay mineral interfaces. Such assessment demands a mobile compound with strong affinity to clay surfaces that is alien to the subsurface. EXPERIMENT: We approached this challenge by using poly(ethylene glycol) (PEG) as interfacial tracer in limestone weathering experiments. FINDINGS: PEG adsorption and transport was dependent on the availability of clay mineral surfaces and carbonate dissolution dynamics. In addition, PEG adsorption featured adsorption-desorption hysteresis which retained PEG mass on clay mineral surfaces. This resulted in different PEG transport for experiments conducted consecutively in the same porous medium. As such, PEG transport was reconstructed with a continuum-scale model parametrized by a Langmuir-type isotherm including hysteresis. Thus, we quantified the influence of exposed clay mineral surfaces on the transport of organic colloids in carbonate media. This renders PEG a suitable model colloid tracer for the assessment of clay surface exposition in porous media.

RESUMEN

Phosphoric acid is used as a chemical activator to prepare coconut shell carbon (PCSC), and for investigating rhodamine B (RhB) adsorption performance. The optimal conditions for the preparation of PCSC (calcined temperature, phosphoric acid concentration), and the influence of adsorption conditions (concentration, pH, etc.) on RhB and the recovery performance of optimal carbon are investigated. Experimental results show that when the amount of PCSC (600 °C, 2 h) is 0.2 g, the initial RhB concentration is 10 mg/L, pH = 6, and the adsorption time is 30 min, it can have 95.84% RhB adsorption efficiency. Liquid ultraviolet spectroscopy also supports this adsorption performance. Characterization data showed that hydroxyl and ester groups, aromatic structures, and PO43- existed on the surface of PCSC, and the amount decreased with increasing calcined temperature. PCSC has a BET (N2) surface area of 408.59 m2/g and has a micropore distribution, EDS-detected P content is 3.91%. SEM showed that the PCSC formed micropores which could better adsorb RhB. The kinetic and thermodynamic analysis of the adsorption of RhB by PCSC showed that the adsorption process was in accord with quasi-secondary kinetic equations and ΔGθ was between -1.65 and -18.75 kJ/mol. The adsorption was a physical adsorption and a spontaneous endothermic reaction, and the obtained PCSC sorption isotherms were classified as Langmuir-type. The RhB adsorption mechanism on PCSC includes pore diffusion, hydrogen bonding, and π-π conjugation. The PCSC prepared by H3PO4 modification has superior adsorption and recycling performance for RhB, providing a reference for the preparation of other biomass carbon materials for the treatment of dye wastewater.

RESUMEN

The zirconium metal - organic framework MIP-202(Zr), based on L-aspartic acid, was prepared by hydrothermal method and used for study of ruthenium adsorption from aqueous solutions. The obtained material was characterized by X-ray diffraction (XRD), infra red spectroscopy (IR), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). The batch adsorption experiment was performed for determination of adsorption equilibrium, kinetics and thermodynamics parameters to Ru(III) from aqueous solution on MIP-202(Zr). The data of ruthenium sorption onto MIP-202(Zr) were fitted and analyzed by the Langmuir, Freundlich and Temkin equilibrium isotherm models, while the Langumir adsorption isotherm models fit the best. Kinetic data were analyzed by four kinetic models, and ruthenium sorption on MIP202(Zr) can be describes the best by intra particle diffusion (Weber Morris). Analysis of thermodynamic properties of ruthenium ions sorption onto MIP-202(Zr) shows that the sorption process has a spontaneous and endothermic nature and is energetically beneficial.

RESUMEN

Arsenic contamination in aqueous media is a serious environmental problem, especially in developing countries. In this research, the Box-Behnken response surface methodology was used to optimize the most relevant variables affecting arsenic adsorption on the ZnO-halloysite surface, including temperature, adsorbent dosage, pH, contact time, and As (III) initial concentration. The regression analysis indicated that the experimental data were appropriately fitted to a quadratic model with the adjusted R-squared value (R2) of 0.982 for As(III) adsorption capacity and a linear model with R2 of 0.931 for As(III) removal. The p-values for both adsorption capacity and removal efficiency were below 0.05, with F-values of 116.91 and 115.58, respectively, supporting the model's validity. The optimum conditions for maximum removal of As(III) were determined through numerical and graphical optimization using the desirability function. It was found that the optimum conditions for adsorption were pH = 7.99, contact time of 3.99 h, As(III) initial concentration of 49.96 mg/L, and adsorbent dosage of 0.135 g/40 ml. The accuracy of the optimization procedure was confirmed by a confirmatory experiment, which showed a maximum arsenic removal of 91.31% and an adsorption capacity of 12.63 mg/g under optimized conditions. Moreover, XPS analysis was performed at different pH levels to investigate the As (III) adsorption mechanism. The results demonstrated that As(III) adsorption occurs at acidic and neutral pH levels. On the other hand, when pH is increased to 8, As (III) oxidizes to As (V), and then adsorption occurs.

RESUMEN

A novel hybrid hydrogel bead (HHBFe) composed of polyvinyl alcohol/sodium alginate/gelatin/quaternary ammonium chitosan (PVA/GA/SA/QCS) and Fe3O4 magnetic nanoparticles was synthesized through green cross-linking of Ca2+ and tannic acid (TA) combined freeze-thaw method. HHBFe exhibited a good spherical shape, porosity, magnetic properties, and excellent mechanical properties and durability. The adsorption capacity of HHB and HHBFe towards methyl orange (MO), tetracycline (Tc), and Cr (VI) was systematically studied and compared. Results revealed similar adsorption capacities for MO and Cr (VI) between HHB and HHBFe, while the presence of Fe3O4 significantly enhanced Tc adsorption, indicating the versatile adsorption functions of HHBFe. Adsorption kinetic followed the pseudo-second-order model, with external diffusion and intra-particle diffusion controlling process. The adsorption data were consistent with the Langmuir isothermal adsorption model, indicating predominantly monolayer adsorption of pollutants by beads. Notably, the beads exhibited easily regenerated, maintaining 60 % of initial adsorption capacity after 5 cycles, particularly for Tc and Cr (VI). The good adsorption performance of HHBFe can be attributed to the strong interaction between their multi-functional groups including phenolic hydroxyl groups, carboxyl groups, amino groups, etc., and pollutant molecules. The multifunctional HHBFe beads prepared in this study and the results obtained with three completely different types of pollutants provide reliability support for their use in different wastewater treatment fields and even in the field of drug carriers.

RESUMEN

Lignin, an abundant natural resource, has not been effectively utilized. In this study, the functionality of lignin was enhanced through amination to produce amine-crosslinked lignin, and its adsorption behavior toward cationic and anionic dyes was investigated. Chemical structure analysis confirmed the successful introduction of amine groups, thereby improving the molecular weight and thermal stability of the optimized amine-crosslinked lignin. Additionally, the amine-crosslinked lignin exhibited a larger specific surface area than kraft lignin, as well as excellent adsorption capacity for both anionic and cationic dyes. Furthermore, it selectively adsorbed anionic and cationic dyes depending on pH conditions. The adsorption kinetics were described using a pseudo-second-order model, and the adsorption isotherms for congo red and methyl green were determined using the Langmuir and Freundlich equations, respectively. Additionally, the reusability and adsorption efficiency of the optimized amine-crosslinked lignin were evaluated, confirming its stable and repeatable adsorption efficiency for congo red and methyl green even after five repeated cycles. The assumed adsorption mechanism was attributed to electrostatic interactions. Therefore, the successful synthesis and excellent adsorption properties of amine-crosslinked lignin suggest its promising potential for environmentally friendly and efficient removal of both cationic and anionic dyes, thereby offering a sustainable solution for wastewater treatment and remediation.

RESUMEN

This research developed a novel composite of MOF-NH2 and graphene oxide (GO) for enhanced CO2 capture. Employing the response surface methodology-central composite design (RSM-CCD) for experiments design, various MOF-NH2/GO samples with GO loadings from 0 to 30 wt% were synthesized. The results of SEM, XRD, EDS, and BET analysis revealed that the materials maintained their MOF crystal structure, confirmed by X-ray diffraction, and exhibited unique texture, high porosity, and oxygen-enriched surface chemistry. The influence of temperature (25-65 °C) and pressure (1-9 bar) on CO2 adsorption capacity was assessed using a volumetric adsorption system. Optimum conditions were obtained at weight percent of 22.6 wt% GO, temperature of 25 °C, and pressure of 9 bar with maximum adsorption capacity of 303.61 mg/g. The incorporation of amino groups enhanced the CO2 adsorption capacity. Isotherm and kinetic analyses indicated that Freundlich and Fractional-order models best described CO2 adsorption behavior. Thermodynamic analysis showed the process was exothermic, spontaneous, and physical, with enthalpy changes of - 16.905 kJ/mol, entropy changes of - 0.030 kJ/mol K, and Gibs changes energy of - 7.904 kJ/mol. Mass transfer diffusion coefficients increased with higher GO loadings. Regenerability tests demonstrated high performance and resilience, with only a 5.79% decrease in efficiency after fifteen cycles. These findings suggest significant potential for these composites in CO2 capture technologies.

RESUMEN

Herein, a novel sulfur-doped carbon material has been synthesized via a facile and sustainable single-step pyrolysis method using lignin-sulfonate (LS), a by-product of the sulfite pulping process, as a novel carbon precursor and zinc chloride as a chemical activator. The sulfur doping process had a remarkable impact on the LS-sulfur carbon structure. Moreover, it was found that sulfur doping also had an important impact on sodium diclofenac removal from aqueous solutions due to the introduction of S-functionalities on the carbon material's surface. The doping process effectively increased the carbon specific surface area (SSA), i.e., 1758 m2 g-1 for the sulfur-doped and 753 m2 g-1 for the non-doped carbon. The sulfur-doped carbon exhibited more sulfur states/functionalities than the non-doped, highlighting the successful chemical modification of the material. As a result, the adsorptive performance of the sulfur-doped carbon was remarkably improved. Diclofenac adsorption experiments indicated that the kinetics was better described by the Avrami fractional order model, while the equilibrium studies indicated that the Liu model gave the best fit. The kinetics was much faster for the sulfur-doped carbon, and the maximum adsorption capacity was 301.6 mg g-1 for non-doped and 473.8 mg g-1 for the sulfur-doped carbon. The overall adsorption seems to be a contribution of multiple mechanisms, such as pore filling and electrostatic interaction. When tested to treat lab-made effluents, the samples presented excellent performance.

RESUMEN

We explain here that the authors of the article cited in the title have misrepresented the species of As(III) and As(V) in solutions and, in particular, have neglected their speciation as a function of pH. Their discussion of (ad)sorption mechanisms is therefore unsatisfactory, especially since organic matter (flower waste) and the presence of iron oxyhydroxides should be taken into account. Furthermore, the modeling of (ad)sorption kinetics and isotherms was based on linearized equations, whereas the corresponding nonlinear equations should have been used. Therefore, we believe that the authors of the original article should make corrections and additions to it. This Letter to the Editor is motivated by a concern to avoid the dissemination of approximate or even incorrect concepts in the scientific literature, which could mislead novice researchers.

RESUMEN

In this study, a high-Si (Si) adsorbent (APR@Sam) was prepared by acid leaching slag (APR) from lead-zinc (Pb-Zn) tailings based on high-temperature alkali melting technology. The synthesized Si-based materials were applied to aqueous solutions contaminated with Pb and cadmium (Cd) to investigate the crucial role of active Si in sequestering heavy metals. The adsorption capacities of APR@Sam and the Si-depleted material (APR@Sam-NSi) were studied under different pH and temperature conditions. The results showed that as the pH increased from 3 to 7, the adsorption capacity increased, the active Si content in the solution increased by 63 %, and the maximum pH of the solution after adsorption was 7.12. After the removal of active Si, the Pb (II) and Cd (II) adsorption capacities of APR@Sam decreased by 45 % and 11.96 %, respectively. OH- promoted the release of Si into the solution, enhancing the material's adsorption efficiency. The reaction mechanism is mainly attributed to surface complexation guided by Si-O and Si-O-Si bonds, metal cation exchange, and bidentate coordination. The results indicated that the Si component is critical for the removal of Pb (II) and Cd (II) by APR@Sam and provide valuable insights into resource recovery strategies from leaching residues.

RESUMEN

Developing recyclable adsorbents for co-capture of I2 and CH3I gas is a meaningful and challenging topic. Herein, Cu0-based mesoporous silica (C-S) materials were synthesized and applied for CH3I capture for the first time. Factors (Cu0 content, temperature, contact time and CH3I concentration) affecting the adsorption behavior were investigated. The results demonstrated that the CH3I adsorption capacity of the obtained C-S materials reached up to 1060 mg/g at 200 â„ƒ. Furthermore, the C-S material exhibited excellent reusability (91.3 %, 5 cycles). It was found that Cu0 could cleave the carbon iodine bonds, causing CH3I to dissociate into •CH3 and I-. Then the Cu+ converted from Cu0 reacted with I- to achieve the purpose of CH3I capture. The adsorption mechanism of CH3I on the C-S materials could be concluded that Cu0 reacted with CH3I form CuI (Cu + CH3I → CuI + •CH3). This work suggested that the obtained C-S materials could be promising adsorbents for CH3I capture.

RESUMEN

Using biochar for dye wastewater treatment is attracting interest due to its excellent adsorption properties and low costs. In this work, a novel biochar derived from oxytetracycline fermentation residue (functionalized OFR biochar, FOBC) was investigated as a efficient adsorbent for typical dyes removal. At 25 °C, the maximum adsorption capacity calculated by Langmuir model of FOBC-3-600 for methylene blue (MB), malachite green (MG), and methyl orange (MO) reached 643.97, 617.89, and 521.03 mg/g, respectively. The kinetics and isotherm model fitting showed that the chemisorption and physisorption both occurred during the adsorption process. Dyes were efficiently adsorbed through pore filling, electrostatic attraction, π-π interactions, and surface complexation. And the cycling experiment and environmental risk assessment indicated that the FOBC-3-600 had excellent recyclability and utilization safety. Overall, this study provides a practical method to simultaneously treat the dyeing wastewater and utilize the antibiotic fermentation residue.

RESUMEN

Zeolites possess a microporous crystalline structure, a large surface area, and a uniform pore size. Natural or synthetic zeolites are commonly utilized for adsorbing organic and inorganic compounds from wastewater because of their unique physicochemical properties and cost-effectiveness. The present review work comprehensively revealed the application of zeolites in removing a diverse range of wastewater contaminates, such as dyes, heavy metal ions, and phenolic compounds, within the framework of contemporary research. The present review work offers a summary of the existing literature about the chemical composition of zeolites and their synthesis by different methods. Subsequently, the article provides a wide range of factors to examine the adsorption mechanisms of both inorganic and organic pollutants using natural zeolites and modified zeolites. This review explores the different mechanisms through which zeolites effectively eliminate pollutants from aquatic matrices. Additionally, this review explores that the Langmuir and pseudo-second-order models are the predominant models used in investigating isothermal and kinetic adsorption and also evaluates the research gap on zeolite through scientometric analysis. The prospective efficacy of zeolite materials in future wastewater treatment may be assessed by a comparative analysis of their capacity to adsorb toxic inorganic and organic contaminates from wastewater, with other adsorbents.

Asunto(s)

RESUMEN

The saline wastewater produced in industrial activities and seawater use would flow into wastewater treatment plants and affect the characteristic of extracellular polymeric substance (EPS) of activated sludge, which could potentially impact the removal of antibiotics via adsorption. Nonetheless, the effect of salinity on trimethoprim adsorption by activated sludge extracellular polymeric substances at trace concentration and the underlying mechanism remain largely unknown. In this study, the effect of salinity on the adsorption removal of a typical antibiotic, i.e., trimethoprim (TMP) at trace concentration (25.0 µg/L) was evaluated. The results showed the content of EPS was decreased significantly from 56.36 to 21.70 mg/g VSS when the salinity was increased from 0 to 10 g/L. Protein fractions occupied the predominant component of EPS, whose concentration was decreased from 38.17 to 12.83 mg/g VSS. The equilibrium adsorption capacity of activated sludge for TMP was decreased by 49.70% (from 4.97 to 2.50 µg/g VSS). The fluorescence quenching results indicated the fluorescence intensity of tryptophan-like substances was decreased by 30% and the adsorption sites of EPS were decreased from 0.51 to 0.21 when the salinity was increased. The infrared spectrum and XPS results showed that the nitrogen-containing groups from protein were decreased significantly. The circular dichroic analysis showed α helix structure of protein in EPS was decreased with the increase of salinity, which was responsible for the decrease of adsorption capacity for TMP.

Asunto(s)

RESUMEN

Due to the serious threat posed by tebuconazole to the aquatic ecosystem, it is imperative to develop a highly efficient adsorbent material for the sustainable remediation of tebuconazole-contaminated water. Herein, a phosphorus (P)-doped biochar from corn straw and H3PO4 was fabricated by one-step pyrolysis for tebuconazole adsorption. Results showed that the P-doped biochar produced at 500℃ (PBC500) possesses a large specific surface area (SSA=869.6 m2/g), abundant surface functional groups, and the highest tebuconazole adsorption capacity (429.6 mg/g). The adsorption of tebuconazole on PBC500 followed pseudo-second-order kinetics and Langmuir adsorption isotherm models. Thermodynamic calculations indicated that the adsorption of tebuconazole by PBC500 was a spontaneous, endothermic process with a random increase. Adsorption mechanism mainly involves pore filling, π-π interactions, hydrogen bonding, and hydrophobic interaction. Moreover, PBC500 demonstrated robust anti-interference capabilities in adsorbing tebuconazole from diverse water sources and exhibited excellent reusability, underscoring its potential for a broad array of practical applications.

Asunto(s)

RESUMEN

Foodborne heterocyclic aromatic amines (HAAs) are potent mutagens and carcinogens, posing significant health risks. Existing enrichment methods for HAAs need better adsorption selectivity and capacity for daily exposure assessment. This study hypothesized that introducing carboxylic groups into magnetic covalent organic frameworks (m-COFs) would improve HAAs adsorption by providing additional binding sites. Hence, we prepared a novel magnetic adsorbent, termed as Fe3O4@DOPA-TpPa-(COOH)2 capable of enhancing the HAAs detection through magnetic solid-phase extraction (MSPE) coupled with UPLC-MS. This sorbent demonstrated a large specific surface area (130.7 m2/g), high magnetic responsivity (21.05 emu/g), and robust stability, with an adsorption capacity (Qm[cal]: 81.82 mg/g) driven by electrostatic, LP - π/C-H - π interactions, and hydrogen bonding. Optimal MSPE conditions provided sensitive detection with a broad linear range (5-500 ng/mL), low limits of detection (0.01-7.01 ng/g), and excellent repeatability. Application to Cantonese mooncake samples showed satisfactory recoveries (62.12%-126.86%). This method offers a more accurate tool for detecting HAAs.

Asunto(s)

RESUMEN

The flocculation of dyeing wastewater generated a large amount of sludge that was often disposed as refractory hazardous waste. The resource utilization of flocculation sludge was of great significance in terms of low treatment cost of sludge, low environmental risk and high usage efficiency of reactive dyes. Herein, a flocculation sludge-derived (FSD) adsorbent was prepared via cross-linking of flocculation sludge yielding by carboxymethyl chitosan-based flocculants and dyes. FSD adsorbent had excellent selective adsorption performance for methylene blue (MB) treatment. The highest removal rate of MB and adsorption capacity of FSD adsorbent were 96.48 % and 354.7066 mg/g, attributing to its rich functional groups, negative charges and special micropore structure. FSD adsorbent owned the favorable regeneration efficiency and stability. Its removal rate of MB was still above 71.8 % after 6 regeneration-adsorption cycles. Its leaching rate of dyes was only 0.0016 mg/mg that was rather lower than common dried flocculation sludge. The adsorption processes of FSD adsorbent were complex in accordance with its characteristics, adsorption isotherms, adsorption kinetics and theoretical calculation. Multiple adsorption mechanisms were present in the treatment of dyeing wastewater by FSD adsorbent. The resource utilization of flocculation sludge, as adsorbents, was a potential candidate in field application.

Asunto(s)