According to circular bioeconomy principles, the use of kiwi peels to remove Direct Blue 78 (DB) from water is investigated during this work, proposing food waste as a recyclable adsorbent substrate.
In this work, the great performance of chitosan-based films blended with TiO2 (CH/TiO2) is presented to adsorb the hazardous pollutant 2,4-dinitrophenol (DNP) from water. The DNP was successfully removed, with a high adsorption %: CH/TiO2 exhibited a maximum adsorption capacity of 900 mg/g. For pursuing the proposed aim, UV–Vis spectroscopy was considered a powerful tool for monitoring the presence of DNP in purposely contaminated water. Swelling measurements were employed to infer more information about the interactions between chitosan and DNP, demonstrating the presence of electrostatic forces, deeply investigated by performing adsorption measurements by changing DNP solutions’ ionic strength and pH values. The thermodynamics, adsorption isotherms, and kinetics were also studied, suggesting the DNP adsorption’s heterogeneous character onto chitosan films. The applicability of pseudo-first- and pseudo-second-order kinetic equations confirmed the finding, further detailed by the Weber–Morris model. Finally, the adsorbent regeneration was exploited, and the possibility of inducing DNP desorption was investigated. For this purpose, suitable experiments were conducted using a saline solution that induced the DNP release, favoring the adsorbent reuse. In particular, 10 adsorption/desorption cycles were performed, evidencing the great ability of this material that does not lose its efficiency. As an alternative approach, the pollutant photodegradation by using Advanced Oxidation Processes, allowed by the presence of TiO2, was preliminary investigated, opening a novel horizon in the use of chitosan-based materials for environmental applications.
Using a water-insoluble β-cyclodextrin-epichlorohydrin copolymer (β-EPI) as an adsorbent to remove carbamazepine (CBZ), an anti-epileptic drug often found both in hospital and urban wastewater, has been validated. The effect of several physicochemical parameters on CBZ retention onto β-EPI, such as contact time, adsorbent dosage, CBZ initial concentration, pH, salts, and temperature, was assessed. The adsorption process occurs in a very short time, less than 20 min, and depends on CBZ concentration and β-EPI amount used. Changes in pH and salt presence, regardless of the type of cation or anion used, do not significantly affect the system’s efficiency. Desorption experiments were also performed, and methanol has proven to be the best CBZ extraction medium; it was also found that the polymer can be recovered and reused for at least five cycles, which makes it cheap and environmentally friendly. Advanced oxidation processes were also tested for CBZ removal by synthesizing a β-EPI polymer bearing titanium dioxide for adsorption and consecutive photocatalytic degradation of the retained pollutant directly onto the material; the effect of TiO2 amount in the polymer on CBZ oxidation was evaluated. These experiments highlighted the system’s effectiveness, and it was also observed that the H2O2 presence in the solution enhanced the CBZ photodegradation.
This work aims to characterize the adsorption process of propranolol HCl, an emerging pollutant and a widely used β-blocker, onto kiwi peels, an agricultural waste. The use of UV-vis spectroscopy was considered to obtain information about the pollutant removal working in the in-batch mode. In a relatively short time, the adsorption process could remove the pollutant from water. A kiwi peel maximum adsorption capacity of 2 mg/g was obtained. With the perspective of scaling up the process, preliminary in-flux measurements were also performed. The investigation of the whole in-batch adsorption process was conducted by studying the effect of ionic strength (adopting salt concentrations from 0 to 0.4 M), pH values (from 2 to 12), adsorbent/pollutant amounts (from 25 to 100 mg and from 7.5 to 15 mg/L, respectively), and temperature values (from 289 to 305 K). The thermodynamics, the adsorption isotherms, and the kinetics of the adsorption process were also carefully investigated. The Langmuir model fitted the experimental data well, with an R2 of 0.9912, restituting KL: 1 L/mg and Q0: 1.8 mg/g. The temperature increase enhanced the pollutant removal due to the endothermic adsorption characteristics. Accordingly, a ΔH°298K of +70 KJ/mol was obtained. The pseudo-first-order kinetic model described the process. Due to the results observed during the study of the effects of pH and ionic strength, the prominent presence of electrostatic interactions, working in synergy with hydrophobic forces and H-bonds between the pollutant and kiwi peel surfaces, was successfully demonstrated. In particular, FTIR-ATR measurements confirmed the latter findings. Finally, desorption experiments for recycling 100% of propranolol for each cycle were performed using 0.1 M MgCl2. Ten cycles of adsorption/desorption were obtained and indicated that the percentage of propranolol removal was not affected during each run, increasing the maximum adsorption from 2 to 20 mg/g.
Due to their properties, snail slime-based products have been appreciated and used worldwide. So, as an alternative and innovative use of snail slime, it was adopted to induce gold nanoparticles' formation, conferring them interesting properties. By a simple, one-pot, and eco-friendly approach, 14 +/- 6 nm wide hybrid gold nanoparticles, having an inorganic metallic core decorated by the slime's main components, were obtained. Among their several properties, their antioxidant and tyrosinase inhibition activity were investigated through the DPPH and ABTS and the tyrosinase assays, respectively. After assessing their non-cytotoxicity in our previous work, the results revealed positive responses, enabling their use as a potential novel multifunctional ingredient in cosmetics. Interestingly, the gold nanoparticle photostability, investigated by means of a solar simulator lamp, suggests using them in commercial cosmetic sunscreen products as a potential alternative to the commonly used inorganic sunscreen ingredients. The theoretical Sun Protection Factor was evaluated, obtaining values in the range 0-12. The proposed environmentally friendly and cost-effective protocol for nanoparticle synthesis, following the principles of Green Chemistry, opens a hugely attractive space toward the study of snail slimebased gold nanoparticles as a potential multipurpose platform in cosmetics.
Amino-grafted Mobil Composition of Matter N. 41 (MCM-41/NH2) and Santa Barbara Amorphous (SBA-15/NH2) type mesoporous adsorbents were successfully used and compared in this work to remove azo dyes (and their mixture) from highly colored solutions. This paper reports a very fast removal and recycle (in 5 min) of great amounts of textile dyes (about the 100%) by materials characterized by high adsorption/desorption capacities. A q(max)approximate to 250 mg/g for each adsorption cycle, that should be potentially increase to approximate to 1250 mg/g, under appropriate experimental conditions, was found for the proposed adsorbents. The UV-Vis absorption spectra of dyes were used to support this finding, determining the rate of adsorption. Several parameters affecting the adsorption process were investigated: the contact time, dyes solution pH values and amount of the adsorbent materials, ranging from 0.4 mg to 12 mg, and dyes (5 x 10(-5)M and 1 x 10(-5)M). Further, the Nitrogen adsorption/desorption isotherms, SAXS patterns, TG analyses, Zeta-potential measurements and microscopic imaging techniques, such as SEM and TEM, were used to detail the nature of interaction between dyes and adsorbents, and to investigate the morphology and the mesoporous array of the amino grafted MCM-41 and SBA-15. (C) 2020 Elsevier B.V. All rights reserved.
Due to the negative effects of emerging contaminants on the environment, that can potentially induce deleterious effects in aquatic and human life, this paper focuses on the removal from the water of Furosemide, through the adsorption process. Indeed, only a few papers are available in the literature about the Furosemide adsorption and, chitosan films are thus proposed for this purpose as safe, sustainable, and recyclable adsorbent materials. In the present work, the effects on the adsorption process of several experimental parameters such as the pH values, ionic strength, amount of adsorbent/pollutant, and temperature values were investigated. The kinetics models, isotherms of adsorption, and the thermodynamic parameters were studied showing that the Furosemide physisorption occurred on the heterogeneous Chitosan surface, endothermically (Delta H degrees = +31.27 +/- 3.40 kJ mol(-1)) and spontaneously (Delta S degrees = +150.00 +/- 10.00 J mol(-1) K-1), following a pseudo-second-order kinetic model. The 90% of the pollutant was adsorbed in 2 h, with a maximum adsorption capacity of 3.5 mg x g(-1). Despite these relatively low adsorption capacities, experiments of desorption were performed and 100% of adsorbed Furosemide was recovered by using concentrated NaCl solutions, proposing a low-cost and green approach, with respect to the previous literature relative to the Furosemide adsorption, fundamental for the pollutant recovery and adsorbent reuse.
This paper reports the use of commercial bentonite clay as cheap natural adsorbent for the Carbendazim removal from water. The very fast and quite complete removal (80 % of the pollutant) occurred in 15 min by using 1 g of adsorbent, with a bentonite adsorption capacity of 1.5 mg/g. Around 100 % of the Carbendazim removal can be reached extending the contact time to 60 min. Regarding the sustainability of the process, the recovery of both the emerging pollutant and adsorbent were successfully obtained, lowering the associated costs for a possible industrial scaling up. Indeed, several cycles of adsorption and desorption, in ethanol, on the same adsorbent were performed. The evaluation of various parameters affecting the adsorption process, such as the amount of the pollutant and clay, the pH, temperature, and the effect of salts in solutions, was considered. The adsorption process followed the pseudo-second order kinetic model and the Freundlich and Temkin adsorption isotherms well fitted the experimental data suggesting the heterogeneous character of the Carbendazim physical and chemical sorption on the clay. Preliminary in flux experiments were also presented and by using 2 g of adsorbent, the 100 % removal of the pollutant occurred in 2 s.
Seafood, a delight for many people, is sold in the market as a wide variety of products. However, seafood industries produce many by-products; for example, during the processing, the heads and shells of shellfish are generated as waste. This results in the generation of a large amount of shell waste that is accumulated over time, inducing a major environmental concern. Effective solutions for recycling shell waste should be taken into consideration, and the extraction of commercially useful substances like chitin and its derivates, such as chitosan, could be a valid solution for reducing the seafood waste’s environmental impact. Thus, during this work, we propose the use of chitosan as biowaste, to induce the formation of solid films useful for decontaminating water from emerging pollutants. In particular, ketoprofen was used as a model contaminant, and a high percentage of removal, at least 90%, was obtained in a short time under our experimental conditions. Thus, a comprehensive investigation into the adsorption of ketoprofen onto chitosan film was performed, detailing the nature of the adsorption by studying the effects of pH, temperature changes, and electrolyte presence in the solutions containing the pollutant. The process was found to be pH-dependent, involving meanly electrostatic interactions between the pollutant molecules and chitosan. The endothermic character of the adsorption was inferred. The kinetics of the process was investigated, showing that the pseudo second-order kinetic model best fit the experimental data. A recycling process of the adsorbent was proposed; therefore, the adsorbed pollutant can be recovered by reusing the same adsorbent material for further consecutive cycles of adsorption without affecting the efficiency for ketoprofen removal from water.