Aqueous Environment Research Articles

Comparative analysis of surface phase diagrams in aqueous environment: Implicit vs explicit solvation models.

Identifying the stable surface phases under a given electrochemical conditions serves as the basis for studying the atomistic mechanism of reactions at solid/water interfaces. In this work, we systematically compare the performance of the two main approaches that are used to capture the impact of an aqueous environment, implicit and explicit solvent, on surface energies and phase diagrams. As a model system, we consider the magnesium/water interface with (i) Ca substitution and (ii) proton and hydroxyl adsorption. We show that while the implicit solvent model is computationally very efficient, it suffers from two shortcomings. First, the choice of the implicit solvent parameters significantly influences the energy landscape in the vicinity of the surface. The default parameters benchmarked on solvation in water underestimate the energy of the dissolved Mg ion and lead to spontaneous dissolution of the surface atom, resulting in large differences in the surface energetics. Second, in systems containing a charged surface and a solvated ion, the implicit solvent model may not converge to the energetically stable ionic charge state but remain in a high-energy metastable configuration, representing the neutral charge state of the ion. When these two issues are addressed, surface phase diagrams that closely match the explicit water results can be obtained. This makes the implicit solvent model highly attractive as a computationally-efficient surrogate model to compute surface energies and phase diagrams.

A novel strategy for the synthesis of samarium/europium-metal organic frameworks, and their utilization for detection of Cr3+, Pb2+, and acetone as a luminescent sensor with superior selectivity and sensitivity properties

With outstanding detection selectivity and sensitivity characteristics, samarium/europium-metal organic frameworks (Sm/Eu-MOF) is capable of functioning as a versatile light-emitting sensor particularly for detecting acetone, Cr3+, and Pb2+ in aqueous environment. While considering maximum detectable concentrations of 0.85 μM, 0.46 μM, and 1.04 μM, respectively, competitive energy interactions for acetone, absorption of energy for Cr3+, and substitution of ions for Pb2+ are the elucidated mechanisms of detecting these substances by Sm/Eu-MOF. Successful formulation and synthesis of a core–shell structured Sm/Eu-MOF, which has endurance to acid/alkali conditions and hydration/heat-stability, can be accomplished by utilizing Samarium and Europium nitrate ions, terephthalic acid, and 2, 5-furandicarboxylic acid. The recovery rate of acetone, Cr3+, and Pb2+ detection from real samples were 95.0–101.0 %, 99.8–101.0 %, and 99.9–104.0 %, respectively.

A comprehensive study of the colloidal properties, biocompatibility, and synergistic antioxidant actions of Antarctic krill phospholipids

Excipient selection is crucial to address the oxidation and solubility challenges of bioactive substances, impacting their safety and efficacy. AKPL, a novel ω-3 polyunsaturated fatty acids (PUFAs) esterified phospholipid derived from Antarctic krill, demonstrates unique antioxidant capabilities and synergistic effects. It exhibits pronounced surface activity and electronegativity at physiological pH, as evidenced by a critical micelle concentration (CMC) of 0.15 g/L and ζ-potential of −49.9 mV. In aqueous environments, AKPL self-assembles into liposomal structures, offering high biocompatibility and promoting cell proliferation. Its polyunsaturated bond-rich structure provides additional oxidation sites, imparting antioxidant properties superior to other phospholipids like DSPC and DOPC. Additionally, AKPL augments the efficacy of lipophilic antioxidants, such as alpha-tocopherol and curcumin, in aqueous media through both intermolecular and intramolecular interactions. In sum, AKPL emerges as an innovative unsaturated phospholipid, offering new strategies for encapsulating and delivering oxygen-sensitive agents.

Direct esterification in helical continuous-flow microreactors under an aqueous environment: optimization, reaction kinetics, and process intensification

This study presents an optimized process for producing long-chain alkyl acrylates via direct esterification in a helical continuous-flow microreactor. Addressing the inefficiencies of traditional batch esterification, such as low energy efficiency and slow mass transfer, this method utilizes continuous-flow chemistry for more effective, eco-friendly, and cost-efficient production. The microreactor, with a 10 m long and 0.5 mm diameter helical microchannel, which active volume was 3.925 ml, was examined for its performance influenced by reactant-catalyst ratios, temperature, and residence time. Results show significantly improved yields of myristyl acrylate (over 89 % in 300 s, respectively) while the residence time was 300 s at 110 ± 10 °C, with a molar ratio of 1-tetradecanol to acrylic acid of 1.3 and a catalyst to acrylic acid molar ratio of 0.1. Additionally, a second-order reaction kinetic model was developed to better understand the reaction dynamics in this setup. This research underscores the potential of integrating helical continuous flow with esterification, offering a novel approach to studying these mechanisms.

Removal of Pyrocatechol from Aqueous Solution Using Activated Carbon Coated with Aluminum Nanoparticles by a Green Method

Background: Pyrocatechol, a phenol derivative, is commonly found in industrial effluents at various concentrations due to its extensive use in multiple industries. These toxic compounds are resistant to biological degradation and pose significant threats to environmental and human health when they enter aquatic environments. Objectives: This study explores the removal of pyrocatechol from aqueous solutions using activated carbon coated with aluminum nanoparticles. Methods: Laboratory materials included oak wood (collected from the mountains around Lorestan province, Iran), pyrocatechol, H3PO4, HCl, Al2O3, NaCl, NaOH, graphite oxide, and NH3. This experimental study was conducted on a laboratory scale. Oak wood was used to synthesize activated carbon, while aluminum oxide and oak moss were employed to produce aluminum nanoparticles using a green method. The characteristics of the adsorbents were examined using XRD, FESEM, FTIR, and BET analyses. Parameters such as contact time (5 - 40 min), pH (3 - 11), initial concentration of pyrocatechol (20 - 200 mg/L), adsorbent dose (50 - 250 mg), and ionic strength were investigated. The residual concentration of pyrocatechol was measured using a spectrophotometer at a wavelength of 275 nm. Results: The results indicated that maximum adsorption efficiency was achieved with a pyrocatechol concentration of 100 mg/L, a pH of 7, a contact time of 20 minutes, and an adsorbent dose of 250 mg. Isotherm and kinetic analyses showed that the adsorption data correlated well with the Langmuir model and the pseudo-second-order kinetic model, respectively. Conclusions: Activated carbon derived from oak wood and coated with aluminum nanoparticles using a green method is highly efficient in removing pyrocatechol from aqueous solutions. This method is recommended as an effective, rapid, cost-effective, and environmentally friendly approach for the removal of pyrocatechol from aqueous environments.

Novel liquid dosimeters for low-energy electron beam irradiation in low and medium dose ranges

Low-energy electron beam irradiation, which refers to the treatment of matter with accelerated electrons at energies below 300 keV, is gaining attention for many applications in life sciences. In the scope of vaccine production, low-energy electron irradiation is an efficient and chemical free technology to inactivate viruses. Low-energy electron beam irradiation has also been proposed to be a powerful technique for its use in biotechnological processes. As biotechnological applications operate in an aqueous environment, there is an urgent need for accurate dose quantification in liquids, especially for low (< 500 Gy) and medium doses (500–5000 Gy). This study investigated dye solutions of xylenol orange tetrasodium, 1,9-dimethylmethylene blue, resazurin sodium, and tartrazine for their suitability as radiochromic liquid dosimeters. The solutions were evaluated regarding their dose–response characteristics and storage stability prior to irradiation over a range of pH values and concentrations. The radiochromic dosimeters were irradiated with electrons with maximal energies of 200 keV and dose rates of 6.5 Gy/s to 45 Gy/s. Then, the absorbance was measured and response curves were plotted. The dye solutions of 1,9-dimethylmethylene blue and resazurin sodium covered a low to medium dose range from 100–1500 Gy and 100–1000 Gy, respectively. Tartrazine at pH 4 was suitable for quantification of doses from 100 Gy to 3500 Gy, which covers a wide dose range of biotechnological applications.

Adsorption Isotherms and Thermodynamics of &lt;i&gt;Thymol Blue&lt;/i&gt; Removal from Aqueous Solution Using Native Pear (&lt;i&gt;Dacryodes edulis&lt;/i&gt;) Seed Biomass

The release of dyes into watercourses not only upsets their beautiful nature but also hinders the transmission of sunlight into streams, reducing photosynthesis and resulting in the loss of aquatic life and reduction of water quality. Therefore, there is need to remove such colored substances. One of such dyes is thymol blue. This study was conducted with a view to removing thymol blue (TB) dye from an aqueous solution using a low-cost agricultural biomass, the African native pear (Dacryodes edulis), as the adsorbent. Batch experiments showed that the process was affected by pH, temperature, contact time, and initial thymol blue concentration. Optimum dye adsorption was achieved at pH 12. The data was analyzed using Langmuir and Freundlich isotherm models. The latter isotherm better described this process than the former. The thermodynamic quantities like free energy change (∆G°), enthalpy change (∆H°), and entropy change (∆S°) were also evaluated. It was inferred from the results that the adsorption process was spontaneous, feasible, endothermic in nature, and occured by a physisorption mechanism. These findings indicate that the native peer seed is an efficient biosorbent for thymol blue removal from an aqueous environment.

Construction of Zn0.5Cd0.5S/Bi4O5Br2 Heterojunction for Enhanced Photocatalytic Degradation of Tetracycline Hydrochloride

The development of efficient catalysts with visible light response for the removal of pollutants in an aqueous environment has been a hotspot in the field of photocatalysis research. A Zn0.5Cd0.5S (ZCS) nanoparticle/Bi4O5Br2 ultra-thin nanosheet heterojunction was constructed by ultrasound-assisted solvothermal method. The morphology, structure, and optoelectronic properties of the composite were characterized by scanning electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and UV–vis diffuse reflectance spectra. Under simulated visible light illumination, the photocatalytic performance was evaluated through degradation of tetracycline hydrochloride. Results show that the degradation effect by the optimum ZCS/Bi4O5Br2 catalyst is superior to pure materials with the kinetic constant that is 1.7 and 9.6 times higher than those of Bi4O5Br2 and ZCS, and also has better stability and reusability. Trapping experiments and electron paramagnetic resonance tests find that free radicals in the photocatalytic system are superoxide radicals and holes. This work provides a referable idea for the development of more efficient and recyclable photocatalysts.

Effect of Precursors Concentrations on the Photocatalysis Performance Stability of Electrodeposited ZnO Nanorods and Their Robustness in Aqueous Environments

ZnO nanostructured materials have been widely utilized in several environmental depollution applications. In the current work, ZnO nanorods were grown using the electrodeposition method with different precursor concentrations. A variation in the dimensions of the nanorods grown with the different precursor concentrations was noticed, as expected. The ability of the fabricated nanorods to remove water pollutants under UV irradiation and their photocatalytic performance stability was also evaluated over a prolonged period of time. Interestingly, the samples grown in different conditions exhibited different capabilities to maintain their morphology and their photocatalytic performance after they were kept in contaminated water for a long time. Moreover, some samples also were found to remain photocatalytically active for approximately 47% longer than other samples. These findings indicate that the performance stability of ZnO nanorods for pollutants removal and their robustness can be greatly improved by controlling their growth parameters, which will favorably impact the use of ZnO nanorods for water-treatment applications and their economic aspects.

Combined effects of pH and dissolved organic matter on the availability of pharmaceuticals and personal care products in aqueous environment

The interaction between pharmaceuticals and personal care products (PPCPs) with dissolved organic matter (DOM) can alter their bioavailability and toxicity. Nevertheless, little is known about how pH and DOM work together to affect the availability of PPCPs. This study investigated the impact of pH and DOM on the availability of seven PPCPs, namely Carbamazepine, Estrone, Bisphenol A, Testosterone Propionate, Triclocarban, 4-tert-Octylphenol and 4-n-Nonylphenol, using negligible depletion solid-phase microextraction (nd-SPME). The uptake kinetics of PPCPs by the nd-SPME fibers increased proportionally with DOM concentrations, likely due to enhanced diffusive conductivity in the unstirred water layer. At neutral pH, the partitioning coefficients of PPCPs for Humic Acid (log KDOC 3.87–5.25) were marginally higher than those for Fulvic Acid (log KDOC 3.64–5.11). Also, the log KDOC values correlated linearly with the log DOW (pH 7.0) values of PPCPs, indicating a predominant role for hydrophobic interactions in the binding of DOM and PPCPs. Additionally, specific interactions like hydrogen bonding, π-π, and electrostatic interactions occur for certain compounds, influenced by the polarity and spatial conformation of the compounds. For these ionizable PPCPs, the log DDOC values exhibit a strong dependence on pH due to the dual influence of pH on both DOM and PPCPs. The log DDOC values rose from pH 1.0 to 3.0, peaked at pH 5.0 to 9.0, and then (sharply) declined from 11.0 to 13.0. The reasons are that in strong acidic circumstances, the coiled and compressed shape of DOM inhibits the hydrophobic interaction, whereas in strong alkaline conditions, significant electrostatic repulsion reduces the sorption. This study reveals that the effects of DOM on the bioavailability of PPCPs are dependent on both pH and the specific compound involved.

Pixelated High-Q Metasurfaces for in Situ Biospectroscopy and Artificial Intelligence-Enabled Classification of Lipid Membrane Photoswitching Dynamics.

Nanophotonic devices excel at confining light into intense hot spots of electromagnetic near fields, creating exceptional opportunities for light-matter coupling and surface-enhanced sensing. Recently, all-dielectric metasurfaces with ultrasharp resonances enabled by photonic bound states in the continuum (BICs) have unlocked additional functionalities for surface-enhanced biospectroscopy by precisely targeting and reading out the molecular absorption signatures of diverse molecular systems. However, BIC-driven molecular spectroscopy has so far focused on end point measurements in dry conditions, neglecting the crucial interaction dynamics of biological systems. Here, we combine the advantages of pixelated all-dielectric metasurfaces with deep learning-enabled feature extraction and prediction to realize an integrated optofluidic platform for time-resolved in situ biospectroscopy. Our approach harnesses high-Q metasurfaces specifically designed for operation in a lossy aqueous environment together with advanced spectral sampling techniques to temporally resolve the dynamic behavior of photoswitchable lipid membranes. Enabled by a software convolutional neural network, we further demonstrate the real-time classification of the characteristic cis and trans membrane conformations with 98% accuracy. Our synergistic sensing platform incorporating metasurfaces, optofluidics, and deep learning reveals exciting possibilities for studying multimolecular biological systems, ranging from the behavior of transmembrane proteins to the dynamic processes associated with cellular communication.

Evaluation of drug release efficiency and antibacterial property of a pH-responsive dextran-based silver nanocomposite hydrogel

The bioavailability of curcumin (CUR), a highly lipophilic and commonly used anticancer drug, is mainly affected by its poor solubility in aqueous environment and quick metabolism. These challenges can be met by employing delivery systems. Nanocomposite materials have been used as delivery systems to enhance the solubility and dissolution rate of the drug. This study aims to develop dextran-graft-poly(4-acryloylmorpholine) silver nanocomposite using a microwave-assisted method to evaluate its drug-release efficiency and antimicrobial activity. The materials were characterized by FT-IR, FE-SEM, EDS, XRD, HR-TEM, TGA, and BET techniques. Drug loading and release efficiency were evaluated using CUR as the model drug. The swelling and drug release studies were conducted in buffer solutions of pH 1.2 and 7.4. Staphylococcus aureus and Escherichia coli were employed to evaluate the antibacterial activity. The cytotoxicity was assessed by MTT assay against the breast MCF-10. Higher swelling and drug release were observed at pH 1.2 than 7.4. Nanocomposite hydrogel exhibited antibacterial activity against the tested bacterial strains. Cytotoxicity study proved the safety of the developed matrix. The results suggest the developed nanocomposite hydrogel to be a promising polymer matrix for the sustained release of CUR for cancer treatment that requires infectious control.

Femtosecond laser structured black superhydrophobic cork for efficient solar-driven cleanup of crude oil

Marine oil spills have become a major global environmental challenge, yet there remains a lack of effective and environmentally friendly strategies for the remediation of water contaminated with high-viscosity oil. In this study, we introduce a superhydrophobic oleophilic material with photothermal properties for efficient absorption of viscous oil. Femtosecond laser treatment methodology is applied to cork (FSLA-cork), which exhibits not only superior hydrophobic and oleophilic properties but also the exceptional ability to be rapidly heated from ambient conditions to 58 °C in 10 s under 1.8 solar irradiation. Under solar irradiance, the FSLA-cork adsorbent functions synergistically by capillary absorption and centrifugal pumping. At one-sun intensity, an oil absorption rate of 4.02 g cm−2 within 200 s was observed. The high adsorption rates of FSLA-cork combined with the high availability of the raw material and its eco-friendly fabrication methods indicate that such methods and materials can be utilized for large-scale clean up of aqueous environments contaminated with high-viscosity oils.

A simple methodology for in situ study of microplastics’ aggregation

AbstractDue to the critical impacts of microplastic (MP) aggregation on their fate, mobility, and bioavailability, this study developed a simple approach to examine their aggregation under varying water chemistry and MPs’ surface aging conditions. An accelerated photodegradation experiment was conducted for 6 weeks. The water chemistry conditions varied by altering pH, using natural organic matter (NOM), and conducting experiments in ultrapure water and synthetic stormwater. The surface chemistry analysis of photodegraded MPs revealed the formation of carbonyl and vinyl functional groups. Zeta potential measurements revealed a more negative surface charge for photodegraded MPs compared to new MPs. The aggregation kinetics of MPs were studied by comparing the number of MP clusters formed over time after intense dispersion in water. The results showed that the presence of NOMs reduces the aggregation tendency of new low‐density polyethylene MPs due to enhanced steric hindrance and electrostatic repulsion. However, variations of pH and utilizing synthetic stormwater versus ultrapure water did not alter the aggregation kinetics of new MPs. The aggregation behavior of photodegraded MPs was significantly different from new MPs. A greater tendency for aggregation of photodegraded MPs was found in the stormwater compared to the ultrapure water. This study contributes to a better understanding of the transport and fate of MPs within the aqueous environment and their subsequent environmental risks.

Host-Guest Complexation of Itraconazole with Cyclodextrins for Bioavailability Enhancement.

Itraconazole is an antifungal agent included in the triazole pharmacological classification that belongs to the BCS class II, characterized by a low solubility in an aqueous medium (of 1 ng/mL, at neutral pH), which is frequently translated in a low oral bioavailability but with a high permeability. In this sense, it is necessary to find solutions to increase/improve the solubility of itraconazole in the aqueous environment. The main purpose of this study is the preparation and analysis of five different guest-host inclusion complexes containing intraconazole. Initially, a blind docking process was carried out to determine the interactions between itraconazole and the selected cyclodextrins. The second step of the study was to find out if the active pharmaceutical ingredient was entrapped in the cavity of the cyclodextrin, by using spectroscopic and thermal techniques. Also, the antifungal activity of the inclusion complexes was studied to examine if the entrapment of itraconazole influences the therapeutic effect. The results showed that the active substance was entrapped in the cavity of the cyclodextrins, with a molar ratio of 1:3 (itraconazole-cyclodextrin), and that the therapeutic effect was not influenced by the entrapment.

Cyclodextrin 'Chaperones' Enable Quasi-Ideal Supramolecular Network Formation and Enhanced Photodimerization of Hydrophobic, Red-shifted Photoswitches in Water.

Precision-engineered light-triggered hydrogels are important for a diversity of applications. However, fields such as biomaterials require wavelength outside the harsh UV regime to prevent photodamage, typically requiring chromophores with extended p-conjugation that suffer from poor water solubility. Herein, we demonstrate how cyclodextrins can be used as auxiliary agents to not only solubilize such chromophores, but even to preorganize them in a 2:2 host-guest inclusion complex to facilitate photodimerization. We apply our concept to styrylpyrene-end-functionalized star-shaped polyethylene glycols (sPEGs). We initially unravel details of the host-guest inclusion complex using spectroscopy and mass spectrometry to give clear evidence of a 2:2 complex formation. Subsequently, we show that the resultant supramolecularly linked hydrogels conform to theories of supramolecular quasi-ideal model networks, and derive details on their association dynamics using in-depth rheological measurements and kinetic models. By comparing sPEGs of different arm length, we further elucidate the model network topology and the accessible mechanical property space. The photo-mediated dimerization proceeds smoothly, allowing to transform the supramolecular model networks into covalent ones. We believe that our strategy opens new avenues for executing hydrophobic photochemistry in aqueous environments with enhanced control over reactivity, hydrogel topology or programmable mechanical properties.

Strategic design, theoretical insights, synthesis, and unveiling antioxidant potential in a novel ascorbic acid analog.

In this study, we investigated the antioxidant potential of a novel ascorbic acid analog, DsD, assessing its interactions with the methylperoxyl (CH3OO·) radical in aqueous and lipid environments. Our focus was on understanding the acid-base equilibrium and how pH affects DsD's primary reaction mechanisms. Our findings indicate a marked preference for hydrogen atom transfer in lipid media, contrasting with sequential proton loss electron transfer (SPLET) in aqueous solutions. Remarkably, DsD's radical scavenging activity significantly outperforms ascorbic acid, being 4.05 and 9469.70 times more potent in polar and lipid contexts, respectively. This suggests DsD's superior efficacy as an antioxidant, potentially offering enhanced protection in biological systems. Additionally, we have demonstrated DsD's synthetic feasibility through a straightforward condensation reaction between ascorbic acid and 1,2-diaminoethane, followed by comprehensive physicochemical and spectroscopic characterization. All computational analyses in this study were conducted using the Gaussian 09 software suite, employing the M05-2X functional and the 6-31 + G(d) basis set. Enthalpy calculations were executed under standard conditions (298.15 K and 1 atm), incorporating appropriate thermodynamic corrections. Rate constants were evaluated using transition state theory (TST), and the overall assessment of radical scavenging activity was guided by the Quantum Mechanics-based Test for Overall Radical Scavenging Activity (QMORSA) protocol.

Study on the applicability of novel molecular targets of Vibrio species by pan-genome mining in the field of nucleic acid detection

Vibrio spp. are ubiquitous in marine areas worldwide and can cause diseases in humans. Aqueous environments favor the transfer of genes between strains, resulting in the loss of strain-specific target genes. This study aimed to explore new molecular targets for the detection of Vibrio strains at the species level using pan-genome analysis for nucleic acid detection and differentiation of major pathogenic Vibrio in aquatic products. Pan-genome analysis and PCR validation revealed a total of 10 specific targets: three for Vibrio parahaemolyticus, one for Vibrio alginolyticus, three for Vibrio vulnificus, three for Vibrio fluvialis. We constructed primers for the selected genes, and we verified their specificity using various Vibrio species and non-Vibrio strains. After systematic optimization, a novel molecular target-based 4-multiplex PCR (4-mPCR) method was developed, exhibiting a detection limit of 103 CFU/mL for pure cultures and 104 CFU/g for fish samples. The initial inoculum was approximately 1 Log10 CFU/g, and all samples were positive after 4 h of enrichment. Not only that, the feasibility of the mined new targets in the field of nucleic acid detection was further validated by the 4-mqPCR and LAMP techniques. These results suggest that novel targets mined by pan-genomic have good generalizability for use in a variety of nucleic acid detection techniques and can help improve the accuracy of nucleic acid-based detection techniques in the detection of pathogenic Vibrio species in aquatic samples, with potential applications for food safety investigations and disease diagnosis.

Remediation of 2,4,6-trichlorophenol from aqueous solution by raw and chemical modified date palm stone biomass: Kinetics and isotherms studies

Raw and citric acid chemically treated date palm stone agro-waste biomass (RDSB and CA-MDSB) powders were used to remove an important class of emerging industrial pollutants, i.e., 2,4,6-trichlorophenol (2,4,6-TCP) from aqueous solutions towards sustainable waste utilization to develop cost-effective technology for treating wastewater. The biomass characterization was performed by using different analytical techniques such as CHN elemental analysis, particle size, BET, FTIR, and SEM-EDX, TGA analysis. The FTIR spectral analysis revealed that the main chemical groups (N–C, O=C, H-O, H-C, and O–C) were involved in trapping 2,4,6-TCP. The highest adsorption was achieved with a contact time of 150 and 120 min, an initial concentration of 50-200 mg/L, and a biosorbent dosage ranging from 0.1 to 1.0 g/L RDSB and CA-MDSB, respectively. The experimental kinetic data of the adsorption process for both adsorbents (RDSB and CA-MDSB) fitted very well with the pseudo-second-order kinetic model and Langmuir equilibrium data. The 2,4,6-TCP maximum monolayer adsorption capacities were 53.7, and 123.8 mg/g for RDSB and CA-MDSB, respectively. The present research confirms that the date palm stone biomass could be used as an effective and low-cost biosorbent for the remediation of 2,4,6-TCP from an aqueous environment.

Study of the Effect of the Surfactant Linear Alkylbenzene Sulfonate (LAS) on the Coagulation of Aged Microplastic

Objective: Evaluate the effect of linear alkylbenzene sulfonate (LAS) surfactant on the coagulation of aged microplastic. Theoretical Framework: Chemical coagulation is one of the steps adopted in water treatment that can help remove microplastics. During coagulation, suspended particles agglomerate, increasing the efficiency of removing these particles in the sedimentation stage. However, when coagulation occurs in the presence of surfactants, evidence points to deficits in removal capacity. Method: Using Jar Test tests, the optimal parameters for microplastic removal were determined with aluminum sulfate as a coagulating agent in the presence and absence of the surfactant linear alkyl benzene sulfonate (LAS). The LAS concentrations studied were in the range of 20 mg/L to 300 mg/L. Microplastic removal efficiency was evaluated by measuring turbidity. Results and Discussions: The combination of pH and coagulant concentration values that best suited the system were 5.0 and 4.25 mg/L, respectively. Due to the addition of surfactants, a decrease in removal efficiency was observed, with an average value ranging from 94.79% to 76.50% due to the interaction of polyethylene spheres with the surfactant. Research Implications: As explained, due to the coexistence of microplastics and surfactants in the aqueous environment, studies that describe chemical coagulation under these conditions have great value for optimizing treatment systems and technologies. Research Originality/Value: The use of aged microplastics aims to approximate their natural occurrence.