Search Results (83)

This study explores the sustainable extraction and application of natural dyes from figs (Ficus carica) and Eucalyptus leaves using an aqueous alkaline medium. The dyeing process was optimized for cotton fabric using the exhaust-dyeing method. Fabrics dyed with Ficus carica extract and its blend with Eucalyptus exhibited enhanced color strength, excellent crocking fastness (rated 4–5), and good washing fastness (rated 3–4 on the gray scale). The use of Aloe barbadensis Miller as a bio-mordant significantly improved dye fixation, resulting in deeper, earthy shades, such as green, yellow–green, and yellowish brown. The highest K/S value (5.85) was recorded in samples treated with a mordant, sodium chloride (NaCl), and the combined dye extracts, indicating a synergistic effect among the components. Mosquito repellency tests revealed that treated fabrics exhibited up to 70% repellency, compared to just 20% in undyed samples. Antibacterial testing against E. coli showed that dyed fabrics achieved over 80% bacterial reduction after 24 h, indicating promising antimicrobial functionality. Air permeability slightly decreased post-dyeing due to the potential shrinkage in cotton fabrics. Furthermore, adsorption studies showed a removal efficiency of 57% for Ficus carica dye on graphene oxide (GO) under ultrasonication. These findings confirm the potential of GO as an effective adsorbent material for treating wastewater from natural textile dyes. Overall, the study highlights the environmental safety, functional performance, and multifunctional advantages of plant-based dyeing systems in sustainable textile applications. Full article

This study evaluates the structural properties and adsorption capacities of four bio-based adsorbents, sawdust (SD), straw (ST), chicken feathers (CFs), and shrimp shells (SSs), for chemical oxygen demand (COD) removal from olive mill wastewater (OMW). Response Surface Methodology (RSM) with a Box–Behnken Design (BBD) was applied to optimize the operational parameters, resulting in maximum COD uptake capacities of 450 mg/g (SD), 575 mg/g (ST), 700 mg/g (CFs), and 750 mg/g (SSs). Among these materials, SSs exhibited the highest COD removal efficiency of 85% under optimal conditions (pH 8, 20 g/L, 30 °C, 5 h, 111 rpm). A mixture design approach was then used to explore the synergistic effects of combining lignocellulosic (SD and ST), chitin-based (SSs), and keratin-based (CFs) adsorbents. The optimized blend (SD 10%, ST 28.9%, SS 38.3%, and CF 22.6%) achieved a COD removal efficiency of 82%, demonstrating the advantage of using mixed biopolymer systems over individual adsorbents. Adsorption mechanisms were investigated through isotherm models (Langmuir, Freundlich, Temkin, and Redlich–Peterson) and kinetic models (pseudo-first-order, pseudo-second-order, Elovich, and intraparticle diffusion). Lignocellulosic adsorbents predominantly followed physisorption mechanisms, while chitin- and keratin-rich materials exhibited a combination of physisorption and chemisorption. Thermodynamic analysis confirmed the spontaneous nature of the adsorption process, with SSs showing the most favorable Gibbs free energy (ΔG = −21.29 kJ/mol). A proposed mechanism for the adsorption of organic compounds onto the bio-adsorbents involves hydrogen bonding, electrostatic interactions, π–π interactions, n–π stacking interactions, hydrophobic interactions, and van der Waals forces. These findings highlight the potential of biopolymer-based adsorbents and their optimized combinations as cost-effective and sustainable solutions for OMW treatment. Full article

This research work focused on the development of an adsorbent biocomposite material based on polyhydroxybutyrate (PHB) and cellulose acetate derived from sugarcane (Saccharum officinarum) fibre, through cellulose acetylation. The resulting material represents both an accessible and effective alternative for the treatment and remediation of water contaminated with heavy metals, such as Ni (II). The biocomposite was prepared by blending cellulose acetate (CA) with the biopolymer PHB using the solvent-casting method. The resulting biocomposite exhibited a point of zero charge (pHpzc) of 5.6. The material was characterised by FTIR, TGA-DSC, and SEM analyses. The results revealed that the interaction between Ni (II) ions and the biocomposite is favoured by the presence of functional groups, such as –OH, C=O, and N–H, which act as active adsorption sites on the material’s surface, enabling efficient interaction with the metal ions. Adsorption kinetics studies revealed that the biocomposite achieved an optimal adsorption capacity of 5.042 mg/g at pH 6 and an initial Ni (II) concentration of 35 mg/L, corresponding to a removal efficiency of 86.44%. Finally, an analysis of the kinetic and isotherm models indicated that the experimental data best fit the pseudo-second-order kinetic model and the Freundlich isotherm. Full article

The development of effective oil adsorbents has attracted a great deal of attention due to the increasingly serious problem of oil pollution. A light and porous collagen (COL)/polyvinyl alcohol (PVA)/vanadium carbide (V₂CT_x) composite aerogel was synthesized using a simple method of blending, directional freezing, and drying. After modification with methyltriethoxysilane (MTMS) via chemical vapor deposition, the aerogel possessed an excellent hydrophobicity and its water contact angle reached 135°. The hydrophobic COL/PVA/V₂CT_x composite aerogel exhibits a porous structure with a specific surface area of 49 m²/g. It also possesses prominent mechanical properties with an 80.5 kPa compressive stress at 70% strain, a low density (about 28 mg/cm³), and outstanding thermal stability, demonstrating a 61.02% weight loss from 208 °C to 550 °C. Importantly, the hydrophobic COL/PVA/V₂CT_x aerogel exhibits a higher oil absorption capacity and stability, as well as a faster absorption rate, than the COL/PVA aerogel when tested with various oils. The hydrophobic COL/PVA/V₂CT_x aerogel has the capacity to adsorb 80 times its own weight of methylene chloride, with help from hydrophobic interactions, Van der Waals forces, intermolecular interactions, and capillary action. Compared with the pseudo first-order model, the pseudo second-order model is more suitable for oil adsorption kinetics. Therefore, the hydrophobic COL/PVA/V₂CT_x aerogel can be used as an environmentally friendly and efficient oil adsorbent. Full article

The deterioration of freshwater ecosystems in anthropogenic wetlands is intensified due to phosphorus inputs from fertilizers applied in agricultural areas. In addition, managing the excess green waste generated in these ecosystems increases the complexity of the problem. To move towards a sustainable society based on the circular economy, the use of controlled combustion of green waste to obtain bioenergy—followed by the application of the resulting ash for phosphorus removal from freshwater bodies via adsorption processes—should be considered. Furthermore, those ashes could be used as natural fertilizers and incorporated into the cultivated fields. This paper presents a deep study of the adsorption of phosphorus ions using ashes from the main green waste produced in wetlands. Various experiments were conducted to determine the effects of different variables in the removal process. A double kinetic model was necessary to explain the presence of two different removal processes. The Langmuir model described the equilibrium isotherm data of both adsorbents through an endothermic process. Acidic pH in the initial solutions was preferred because it promotes phosphorus removal by calcium dissolution. The alkalinity did not have a substantial effect on the adsorbent capacity. Calcium was the element that had a more significant influence on the overall process. Finally, a removal study using blended materials was performed. A combined model was proposed and validated based on the original isotherm models for the pure materials. Full article

One of the approaches to limit the negative impact on the environment from the burning of coal in the production of heat and electricity is to limit their use by blending them with biomass. Blended fuel combustion leads to the generation of a solid ash residue differing in composition from coal ash, and opportunities for its utilization have not yet been studied. The present paper provides results on the carbon capture potential of adsorbents developed through the alkaline conversion of ash mixtures from the combustion of lignite and biomass from agricultural plants and wood. The raw materials and the obtained adsorbents were studied with respect to the following: their chemical and phase composition based on Atomic Absorption Spectroscopy with Inductively Coupled Plasma (AAS-ICP) and X-ray powder diffraction (XRD), respectively, morphology based on scanning electron spectroscopy (SEM), thermal properties based on thermal analysis (TG and DTG), surface parameters based on N₂ physisorption, and the type of metal oxides within the adsorbents based on temperature-programmed reduction (TPR) and UV-VIS spectroscopy. The adsorption capacity toward CO₂ was studied in dynamic conditions and the obtained results were compared to those of zeolite-like CO₂ adsorbents developed through the utilization of the raw coal ash. It was observed that the adsorbents based on ash of blended fuel have a comparable carbon capture potential with coal fly ash zeolites despite their lower specific surface areas due to their compositional specifics and that they could be successfully applied as adsorbents in post-combustion carbon capture systems. Full article

The highly efficient removal of mercury metal ions at a higher pH (basic media) is barely reported in the literature. In this study, we developed a novel adsorbent by blending chitosan with guar gum, designed to effectively remove mercury ions from basic media by stabilizing them with a gold (Au³⁺) solution. The FTIR confirmed the compatibility of chitosan and guar gum through hydrogen bonding. The morphology of the blend exhibited an amorphous and porous structure. A mesoporous structure with a surface area, volume, and diameter of 11.843 (m²/g), 0.184 (cm²/g), and 17.072 nm, respectively, was confirmed by BET. The adsorption behavior was analyzed using isotherms and kinetics models, which best fitted with the pseudo-second-order kinetic model and Freundlich adsorption isotherm model, respectively. The adsorbent was shown to be an excellent candidate for the removal of mercury ions in water, with an adsorption efficiency of 92% at pH 12 in 60 min and a maximum adsorption capacity of 370.37 (mg/g). Full article

Polyphenols are organic molecules extracted from various fruits, such as coffee and citrus, that possess biological activity and antioxidant properties. However, the presence of polyphenols in the environment is hazardous to water quality and living health. Among a variety of water remediation methods, adsorption remains a staple in the field. Therefore, this work aims to develop porous polycaprolactone: poly(methyl methacrylate) (PCL:PMMA) membranes as a support for hydrotalcite immobilization for the removal of chlorogenic acid polyphenol (CGA) from aqueous solutions. Due to the hydrophilic nature of hydrotalcite, the adsorbent was functionalized with hexadecyltrimethylammonium bromide (CTAB) to increase its affinity for CGA, resulting in a removal efficiency of approximately 96%. Composite fiber membranes were prepared by solution-blowing spinning with specific amounts of hydrotalcite added (i.e., 1 to 60 wt%). A 3:1 PCL:PMMA blend resulted in superior mechanical traction (0.8 MPa) and stress deformation (70%) compared to pure PCL (0.7 MPa and 37%) and PMMA (0.1 MPa and 5%) fibers. PCL:PMMA membranes with 60% LDH-CTAB exhibited CGA removal rates equal to 55% in the first cycle while maintaining the capacity to remove 30% of the polyphenol after five consecutive reuses. Removal rates up to 90% could also be achieved with an appropriate adsorbent dose (2 g L⁻¹). Adsorption was found to follow pseudo-second-order kinetics and was adequately described by the Langmuir model, saturating LDH-CTAB active sites in four hours. PCL:PMMA:LDH-CTAB composites can be considered a potential alternative to support adsorbents for water remediation. Full article

The presence of asphaltene, especially in heavy crude oil, causes difficulties in the de-watering/desalting process, which is the initial step of crude oil pretreatment. This study investigates the effect of asphaltenes on the stability of crude oil emulsions using a simulated oil system composed of toluene and n-heptane. It was found that asphaltenes behave like conventional surfactants, adsorbing at the oil–water interface and reducing interfacial tension. The critical aggregation concentration (CAC) of W/O emulsions formed from a toluene and n-heptane mixture (7:3 volume ratio) was found to be 0.05 g/L. When the asphaltene concentration was greater than CAC, the asphaltene aggregated into clusters, forming a viscoelastic interface film that enhanced the strength of the emulsion droplets. At an asphaltene concentration of 0.01 g/L, the storage modulus (G′) and loss modulus (G″) were 1.12 Pa·s and 8.94 Pa·s, respectively. The storage modulus G′ was less than the loss modulus G″, indicating that the viscoelastic nature of the emulsion, and both the G′ and G″ of the emulsions increased with the increasing asphaltene concentration. When the concentration reached 11 g/L, G′ and G″ were 1033 Pa·s and 416 Pa·s, respectively, with G′ exceeding G″, indicating that the emulsion became more stable. Moreover, increasing the solvent aromaticity led to a rise in the CAC of asphaltene, which was favorable for breaking emulsions. The findings imply that reducing the asphaltene content at the interfaces of oil–water by adding an aromatic solvent or blending with light crude oil is a feasible way to break the emulsion and further dewater and desalt. Full article

Starch is one of the most abundant polysaccharides in nature and has a high potential for application in several fields, including effluent treatment as an adsorbent. Starch has a unique structure, with zones of different crystallinity and a glycosidic structure containing hydroxyl groups. This configuration allows a wide range of interactions with pollutants of different degrees of hydrophilicity, which includes from hydrogen bonding to hydrophobic interactions. This review article aims to survey the use of starch in the synthesis of diverse adsorbents, in forms from nanoparticles to blends, and evaluates their performance in terms of amount of pollutant adsorbed and removal efficiency. A critical analysis of the materials developed, and the results obtained is also presented. Finally, the review provides an outlook on how this polysaccharide can be used more effectively and efficiently in remediation efforts in the near future. Full article

With the recent ban on the production and use of long-chain perfluorinated compounds, the development of alternative approaches to prepare liquid-repellent surfaces that avoids the use of such compounds has become an urgent issue. We have succeeded in the development of fish-mimicking hydrophilic transparent hydrogel-based films with long-lasting anti-oil adhesion properties. Such films could be prepared by simply mixing poly(vinylpyrrolidone) (PVP), nanoclay particles (NCPs), and a waterborne aminosilane (AOS) using an integral blend (IB) method. When submerged in water, these films displayed underwater superoleophobicity (advancing and receding contact angles (CAs) of diiodomethane were ~171°/~163°) with low CA hysteresis (less than 8°), because the hydrophilic nature of the films promoted the formation of a thin layer of adsorbed water on the topmost film surfaces, similar to fish scales. Furthermore, when our films were coated onto the inside of poly(ethylene terephthalate) (PET) bottles and pre-wetted using 80 °C hot water vapors, these film surfaces could effectively repel various oils and were able to maintain their oil-repellent properties for more than 5 weeks. These water-driven, non-perfluorinated transparent hydrogel-based films are expected to increase recycling of PET bottles for oils that are generally incinerated or landfilled. Full article

Due to the negative impacts the dye may have on aquatic habitats and human health, it is often found in industrial effluent and poses a threat to public health. Hence, to solve this problem, this study developed magnetic adsorbents that can remove synthetic dyes like methylene blue. The adsorbent, in the form of beads, consists of a polymer blend of chitosan, polyethylene glycol, polyvinyl alcohol, polyvinylpyrrolidone, and superparamagnetic iron oxide nanoparticles (average size of 19.03 ± 4.25 nm). The adsorption and desorption of MB from beads were carried out at pH values of 7 and 3.85, respectively. At a concentration of 9 mg/L, the loading capacity and the loading amount of MB after 5 days peaked at 29.75 ± 1.53% and 297.48 ± 15.34 mg/g, respectively. Meanwhile, the entrapment efficiency of MB reached 29.42 ± 2.19% at a concentration of 8 mg/L. The cumulative desorption capacity of the adsorbent after 13 days was at its maximum at 7.72 ± 0.5%. The adsorption and desorption kinetics were evaluated. Full article

As the atmospheric carbon dioxide (CO₂) concentration rapidly rises, carbon capture, utilization, and storage (CCUS) is an emerging field for climate change mitigation. Various carbon capture technologies are in development with the help of adsorbents, membranes, solvent-based systems, etc. One of the main challenges in this field is the removal of CO₂ from nitrogen (N₂) gas. This paper focuses on mixed matrix membrane technology, for which the CO₂/N₂ separation performance is based on differences in gas permeations. Membrane separation and purification technologies are widely studied for carbon capture. Microporous adsorbents such as zeolites and metal organic frameworks (MOFs) for carbon capture have been attracting researchers’ attention due to their highly porous structures, high selectivity values, and tunable porosities. Utilizing microporous adsorbents dispersed within a novel, blended polymer matrix, fourteen membranes were prepared with the commercial MOF ZIF-8, zeolite 13X, and kaolin, with methyl cellulose (MC) and polyvinyl alcohol (PVA), which were tested using a single gas permeation setup in this study. The addition of polyallylamine (PAH) as a chemisorbent was also investigated. These membranes were synthesized both with and without a polyacrylonitrile (PAN) support to compare their performances. MC was found to be an ideal polymeric matrix component to develop free-standing MMMs. At 24 °C and a relatively low feed pressure of 2.36 atm, a free-standing zeolite-13X-based membrane (MC/PAH/13X/PVA) exhibited the highest N₂/CO₂ selectivity of 2.8, with a very high N₂ permeability of 6.9 × 10⁷ Barrer. Upon the optimization of active layer thickness and filler weight percentages, this easily fabricated free-standing MMM made of readily available materials is a promising candidate for CO₂ purification through nitrogen removal. Full article

Air cleaners with activated carbon (AC) filters for the adsorption of gaseous pollutants are often used to improve indoor air quality. As formaldehyde is a common and health-relevant indoor air pollutant, many testing standards for air cleaners, such as GB/T 18801:2015, require the cleaning efficacy to be tested with this substance. This often persuades manufacturers to optimize the employed filters specifically for formaldehyde. However, in regions where indoor formaldehyde levels are far below the guideline values, other gaseous pollutants might be more relevant. Thus, the question arises of whether the optimization for formaldehyde can have a negative impact on the adsorption of other gases. To address this question, the clean air delivery rate (CADR) of an air cleaner was determined for different test gases with either a standard AC filter or an AC filter modified for improved formaldehyde adsorption. Although the modified AC filter performed substantially better for formaldehyde, a strong reduction in the CADR was observed for toluene and nitrogen dioxide. This is a drawback for situations in which these gases are more problematic than formaldehyde. The findings suggest using either specialized filters for different applications or blends of different adsorbants to find the best compromise for the most relevant pollutants. Full article

The reported work addresses the effect of fillers on the thermodynamic stability and miscibility of compressible polymer blends. We calculate the spinodal transition temperature of a filled polymer blend as a function of the interaction energies between the blend species, as well as the blend composition, filler size, and filler volume fraction. The calculation method relies on the developed thermodynamic theory of filled compressible polymer blends. This theory makes it possible to obtain the excess pressure and chemical potential caused by the presence of fillers. As a main result of the reported work, we demonstrate that the presence of neutral (non-adsorbing) fillers can be used to enhance the stability of a polymer blend that shows low critical solution temperature (LCST) behavior. The obtained results highlight the importance of the osmotic effect of fillers on the miscibility of polymer blends. The demonstrated good agreement with the experiment proves that this effect alone can explain the observed filler-induced change in the LCST. Full article