Adsorption Of Ibuprofen Research Articles

Removal of Ibuprofen from Aqueous Solutions by Using Graphene Oxide@MgO

In this study, a new composite adsorbent, namely magnesium oxide modified graphene oxide (hereafter abbreviated GO@MgO), was prepared for the removal of Ibuprofen (IBU), a non-steroidal anti-inflammatory drug (NSAID) compound. Graphene oxide was modified with MgO to improve its properties. Several factors important for the evolution of the adsorption process were investigated, such as the dose of the adsorbent, the pH, and the initial IBU content, as well as the duration of the procedure and temperature. According to the results obtained, it was found that at pH 3.0 ± 0.1, by applying 0.5 g/L GO@MgO to 100 mg/L IBU, more than 80% was removed, reaching 96.3% with the addition of 1.5 g/L adsorbent in 24 h. After 30 min, the equilibrium was reached (77% removal) by adding 0.5 g/L of GO@MgO. This study proves that GO@MgO is capable of economical and efficient adsorption. The IBU kinetic data followed the pseudo-second-order kinetic model. Langmuir and Freundlich isotherm models were used to interpret the adsorption, but the Freundlich model described the adsorption method more accurately. The positive values of ΔH0 (14.465 kJ/mol) confirm the endothermic nature of the adsorption. Due to the increase of ΔG0 values with temperature, the adsorption of IBU on GO@MgO is considered to be spontaneous.

High-performance novel ZIF-67 and ZIF-67@MWNTs composite adsorbents for efficient removal of pharmaceutical contaminant from water: Exceptional capacity and excellent reusability

The removal of pharmaceutical waste products like ibuprofen (IBP) from water is very important for the environment and the health of human and aquatic organisms. In the present work, the adsorption of IBP from aqueous solution was investigated by synthesizing novel ZIF-67 and ZIF-67@MWNTs hybrid composite material by incorporating ZIF-67 particles with carboxyl functionalized multiwalled carbon nanotubes (COOH-MWNT). The synthesized ZIF-67 and ZIF-67@MWNTs adsorbents were characterized by the XPS, XRD, SEM, TEM, BET, FTIR, and TGA analysis to examine their physio-chemical properties. The synthesized novel ZIF-67 has a 1743 m2/g BET surface and 0.692 cm3/g total pore volume. The IBP adsorption process including isotherm and kinetic studies as well as the effect of different parameters i.e. pH, initial concentration, time, adsorbents, and their dosage were examined. Among all the synthesized composite materials, the ZIF-67@MWNT-50 mg material showed the highest IBP adsorption capacity of 841 ± 5 mg/g, about 467 ± 5 mg/g more than the ZIF-67 following the Langmuir and pseudo-second-order model. The enhancement in the IBP adsorption is because of the incorporation of COOH-MWNT and the presence of a large number of active binding sites which showed the van der Waal interactions, host–guest interactions, π- π interactions, and H-bonding between the adsorbate and adsorbent. For the detailed study of the IBP adsorption mechanism of ZIF-67, molecular dynamic (MD) simulations were performed. Additionally, the reusability of ZIF-67@MWNT-50 mg material via a simple regeneration method up to five cycles while maintaining about 96 % adsorption capacity of the pristine non-used ZIF-67@MWNT-50 mg material revealed its importance as an effective adsorbent for the adsorptive elimination of different pharmaceutical hazardous materials from water.

Performance evaluation of different nitrogenous biomass pyrolysis chars: Physicochemical properties and ibuprofen adsorption

The preparation of high-performance porous carbons (HPPCs) using biomass as adsorbent is a viable strategy for the treatment of ibuprofen (IB) in water. In the present study, pyrolyzed carbon was prepared from duckweed (DW) and rice straw (SW) at 400, 500, and 600 °C, and subsequently mixed pyrolysis with KOH to prepare the HPPCs. The HPPCs were used for the treatment of ibuprofen (IB) in water to evaluate their absorption performance. The physicochemical properties of biochar and HPPCs were investigated using scanning electron microscopy, X-ray electron microscopy, Raman microscopy, and the Brunauer-Emmett-Taylor method. In IB adsorption experiments, adsorption equilibrium was evaluated using Langmuir and Freundlich isotherm models. The maximum adsorption capacities of DW and SW were 0.952 and 0484 g/g, respectively, at an IB concentration of 0.5 g/L. The adsorption capacity of HPPCs for IB is influenced by a multifactorial combination of the specific surface area, nitrogen content, and nitrogen-containing functional groups on the surface. Generally, the HPPCs showed great potential for the removal of the IB pharmaceutical contaminants from aqueous solutions.

Ibuprofen removal by modified natural zeolite: characterization, modeling, and adsorption mechanisms

AbstractBACKGROUNDDeveloping robust technologies to remove emerging pollutants from water is urgent since conventional treatments are not technically prepared to remove them. This paper investigated the ibuprofen (IBU) adsorption capacity onto natural zeolite (NZ) and hydrothermally modified zeolite in an acidic medium followed by impregnation with the cationic surfactant cetyltrimethylammonium bromide (CTAB) (MZHT‐CTAB). The materials characterization included scanning electron microscopy (SEM), X‐ray diffraction (XRD), atomic absorption spectroscopy (AAS), Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA/DTG), N2 adsorption/desorption isotherm (BET), Zeta Potential (ZP), and Point of Zero Charge (pHPZC). The adsorptive capacity studies were carried out by varying the pH solution, a kinetic study at three concentrations (25, 50, and 100 mg L−1), and the contaminant concentration influence (5–100 mg L−1).RESULTSThe results showed that the MZHT‐CTAB obtained both the highest removal efficiency (~ 37%) and the highest adsorption capacity (~ 14 mg g−1) at pH 5.0. The Pseudo Second‐Order (PSO) model, which showed the best fit to the experimental data, is significant as it indicates the reliability of our results. The maximum adsorption capacity for the concentration of 100 mg L−1 was 11.93 mg g−1. According to Giles's classification, the isotherm was classified as S‐3 type, indicating the competition between the adsorbate and water molecules for the active sites on the adsorbent surface.CONCLUSIONThe adsorption studies demonstrate that the novel adsorbent (MZHT‐CTAB) is highly effective in removing IBU, presenting a significant removal capacity and feasibility. This promising result contributes to the ongoing search for alternative materials for water treatment. © 2024 Society of Chemical Industry (SCI).

Postsynthetically Modified Cationic, Robust MOF Featuring Selective Separation of Carboxylate-Containing Pharmaceutical Drugs from Water at Neutral pH: Elucidation of the Adsorption Mechanism by Theory and Experiments.

The escalating levels of hazardous pharmaceutical contaminants, specifically nonsteroidal anti-inflammatory drugs (NSAIDs), in groundwater reservoir surfaces and surface waterway systems have prompted substantial scientific interest regarding their potential deleterious effects on both aquatic ecosystems and human health. Extraction of those pollutants from wastewater is quite challenging. Hence, the development of economic, sustainable, and scalable techniques for capturing and removing those pollutants is crucial to ensure water safety. Herein, we demonstrate a physicochemically stable, reusable, porous Hf(IV)-based cationic metal-organic framework (MOF), namely, 1'@MeCl for the aqueous phase adsorption-based removal of NSAIDs (diclofenac, naproxen, ibuprofen) from the wastewater environment. The highly positively charged surface of the 1'@MeCl MOF enables it to selectively extract more than 99% of diclofenac, naproxen, and ibuprofen contaminants within less than 30 s. With fast adsorption kinetics, very high adsorption capacities (Qe) were achieved at neutral pH for diclofenac (482.9 mg/g), naproxen (295.9 mg/g), and ibuprofen (219.5 mg/g). Moreover, the influence of changes in pH and coexisting anions on the adsorption property of the 1'@MeCl MOF was studied. Furthermore, the adsorption efficiency of 1'@MeCl in different real water environments was ensured by performing diclofenac, naproxen, and ibuprofen adsorption from tap, river, and lake water. Moreover, a 1'@MeCl-anchored cellulose acetate-chitosan membrane was developed successfully to demonstrate the membrane-based extraction of diclofenac, naproxen, and ibuprofen from contaminated water. Furthermore, a molecular-level mechanistic study was performed through experimental and computational study to propose the plausible adsorption mechanisms for diclofenac, naproxen, and ibuprofen over the surface of 1'@MeCl.

Production and characterization of activated carbons from asphaltene by carbon dioxide and steam for ibuprofen adsorption

Production and characterization of activated carbons from asphaltene by carbon dioxide and steam for ibuprofen adsorption

Non-steroidal anti-inflammatory drugs adsorption from aqueous solution by MOFs MIL-100(Fe), ZIF-8 and UiO-66: Synthesis, characterization, and comparative study

Pharmaceutical products such as ibuprofen and naproxen pose a potencial risk to the environment and to the human health. In this context, it is necessary seek and implement new effective and low-cost technologies for water treatment such as adsorption. Metal-organic frameworks (MOFs) emerge as promising adsorbent materials due to their structural diversity and stability. The obtained MOFs were characterized by SEM/EDX, XRD, FTIR, N2 at 77 K, DLS, and PZC. According to the textural parameters, the obtained MOFs have the next surface areas: MIL-100 (Fe) 1359 m2, ZIF-8 357 m2 and UiO-66 1654 m2. Having this differences in surface areas, alongside the different PZC of each materials, affect the adsorption capacity. According to the experimental data UiO-66 and MIL-100(Fe) had the highest ibuprofen adsorption capacity (152.3 mg g-1) and naproxen adsorption capacity (278.3 mg g-1), respectively. On the other hand, ZIF-8 has the lowest adsorption capacity of ibuprofen and naproxen (85.4 and 78.9 mg g-1 respectively). It was found that the best-fitting model according to its R2 for all materials with both adsorbates was the Sips model. Moreover, all materials with all adsorbates, except for UiO-66 with naproxen, reached equilibrium within the first 120 min and fitted the pseudo-second order model. According to thermodynamic parameters and analysis of fitted kinetic models, it was determined that during adsorption, a combination of physical and chemical phenomena occurs, from which the following interactions are proposed as the main adsorption mechanisms: hydrogen bonding, π -π interactions, anion-π interactions, and Lewis’ acid/base interactions.

Valorization of Agave angustifolia Bagasse Biomass from the Bacanora Industry in Sonora, Mexico as a Biochar Material: Preparation, Characterization, and Potential Application in Ibuprofen Removal

The aim of this research was to separate the over-the-counter nonsteroidal anti-inflammatory drug (NSAID), ibuprofen, from an aqueous solution using the adsorption method, as this NSAID is one of the most globally consumed. An adsorbent was crafted from the Agave angustifolia bagasse, a byproduct of the bacanora industry (a representative alcoholic beverage of the state of Sonora, in northwestern Mexico). Three bioadsorbents (BCT1, BCT2, and BCT3) were produced via pyrolysis at a temperature of 550 °C, with slight variations in each process for every bioadsorbent. The bioadsorbents achieved material yields of 25.65%, 31.20%, and 38.28% on dry basis respectively. Characterization of the bagasse and adsorbents involved scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC). The biomass morphology exhibited a cracked surface with holes induced via the bacanora production process, while the surface of the bioadsorbents before ibuprofen adsorption was highly porous, with a substantial surface area. After adsorption, the surface of the bioadsorbents was transformed into a smoother grayish layer. The macromolecules of cellulose, hemicellulose, and lignin were present in the biomass. According to functional groups, cellulose and hemicellulose degraded to form the resulting bioadsorbents, although traces of lignin persisted after the pyrolysis process was applied to the biomass. In an adsorption study, BCT1 and BCT2 bioadsorbents successfully removed 100% of ibuprofen from aqueous solutions with an initial concentration of 62.6 mg/L. In conclusion, the biocarbon derived from Agave angustifolia bagasse exhibited significant potential for removing ibuprofen via adsorption from aqueous solutions.

Optimizing the efficient removal of ibuprofen from water environment by magnetic carbon aerogel: kinetics, isotherms, and thermodynamic studies

Ibuprofen (IBP) is a widely used analgesic and anti-inflammatory drug known to be a pollutant in aquatic environments. In the present work, Magnetic Carbon Aerogel (MCA) was synthesized to remove IBP. Central Composite Design (CCD) approach was applied to study the effect of critical variables, such as pH, contact time, and amount of adsorbent. X-ray diffraction, nitrogen adsorption/desorption, Fourier-transform infrared spectroscopy, emission scanning electron microscopy, and MCA surface charge with zeta-potential analysis were used to characterize the samples. Under optimal conditions (IBP concentration of 10 mg/L, pH 4, MCA dosage of 0.092 g, and contact time of 45 min), a removal efficiency of 98 % was achieved. The most influential parameter on the IBP adsorption was pH. The results showed that the adsorption capacity for MCA was 46.94 mg/g based on Langmuir isotherm (R2 = 0.9998). The kinetic data showed that the adsorption of IBP on MCA was second-order and exothermic (ΔH° = -44949 J/mol). The reusability of the adsorbent was examined through 5 cycles, and no significant loss in the removal efficiency of IBP by MCA was observed.

In-situ and Ex-situ synthesized activated carbons derived from Raphia hookeri Kernels for ibuprofen adsorption in wastewater

This study introduces an innovative approach to synthesizing activated carbon (AC) from Raphia hookeri kernels, optimizing its application for efficient ibuprofen removal from wastewater. By exploring two distinct activation pathways—in-situ and ex-situ—the research underscores the tailored performance of the resulting ACs. Comprehensive characterization included point-of-zero charge (pHpzc), Brunauer-Emmett-Teller (BET) analysis, Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and X-ray diffraction (XRD). BET analysis revealed surface areas of 260.932 and 273.863 m²g⁻¹ for in-situ and ex-situ ACs, respectively, emphasizing their high porosity. The adsorption efficiency was evaluated under various conditions: pH (2−10), adsorbent doses (0.05–0.15 g), contact times (20–200 min), and ibuprofen concentrations (2–10 mgL⁻¹). The ACs demonstrated robust performance in ibuprofen removal, with kinetic data aligning with the pseudo-second-order model. Notably, the in-situ AC exhibited heterogeneous surface and multilayer adsorption characteristics (KF = 13.94 mgg⁻¹), while the ex-situ AC showed monolayer adsorption behavior (qm = 23.14 mgg⁻¹). Both ACs maintained high capacities over multiple cycles, indicating effective regeneration and reuse, making them cost-efficient and sustainable for wastewater treatment. This study's innovation lies in systematically comparing activation pathways, offering a framework for customizing biomass precursors to enhance adsorption in wastewater management.

Granulated graphene oxide-activated carbon for adsorptive removal of diclofenac sodium and ibuprofen in a continuous fixed-bed column

The granular graphene oxide-activated carbon (GGA) composite was synthesized with polyvinyl alcohol (PVA) and malonic acid (MA) as chemical crosslinker at different conditions. GGA synthesis was performed at different parameters including binder-to-powder ratio in the range of 0.5–1.2, synthesis time in the range of 2–24 h, and drying temperature in the range of 60–110 °C. Response surface methodology (RSM) was used to optimize the synthesis parameters of the adsorbent synthesis. The optimum parameters for synthesis were achieved at a binder-to-powder ratio of 0.875, a synthesis time of 23.992 h, and a drying temperature of 60.071 °C. XRD, FTIR, FE-SEM, BET and TGA analyses were used to discuss the characteristics of the adsorbent structures. The surface area and mechanical stability were found to be 156.59 m2/g and 95.417 %, respectively. The adsorption behavior of mono-components (diclofenac sodium (DCF)/ibuprofen (IBP)) and bi-components (DCF + IBP) on the GGA was evaluated in a fixed-bed column. The effects of column operating parameters, including bed mass (m: 0.25–0.75 g), flow rate (Q: 5–9 mL/min), and adsorbate concentration for DCF (C: 20–100 mg/L) and IBP (C: 5–15 mg/L) on the breakthrough curves were investigated. The experimental data of fixed-bed column were correlated with breakthrough models such as Thomas, Bohart-Adams, Yoon-Nelson, Yan, Gompertz, and Log-Gompertz via both linear (under different column operating conditions) and nonlinear (for DCF (Co of 60 mg/L; m of 0.5 g and Q of 7 mL/min) and IBP (Co of 10 mg/L; m of 0.5 g and Q of 7 mL/min)) regression analysis. The maximum adsorption capacities calculated by the Thomas model were 110.068 and 34.912 mg/g for DCF and IBP, respectively. In bi-component systems, antagonistic behavior was observed in the adsorption of DCF and IBP. The results showed that the GGA can successfully remove DCF and IBP through a fixed-bed adsorption column.

Calcium oxide from eggshell wastes for the removal of pharmaceutical emerging contaminant: Synthesis and adsorption studies

The objective of this work is to study the removal efficiency of pharmaceutical emerging contaminant ibuprofen from aqueous environment by using cost-effective material, such as calcium oxide derived from raw eggshell wastes, it is synthesized through calcination process for removal of ibuprofen. The study of the surface morphology and functional groups of the calcium oxide as adsorbent was performed using SEM and FTIR. The study suggests that there are different factors such as contact time, pH, initial concentration and adsorbent dosage influence the adsorptive removal of ibuprofen from aqueous media. The isotherm model such as Langmuir, Freundlich and Temkin were also investigated to study the adsorption equilibrium behaviors of ibuprofen uptake by using calcined eggshell, CaO. Henceforth, the highest removal efficiency of ibuprofen from aqueous solution is 93.72% at contact time of 60 min at pH 10 with initial concentration of 10 mg/L using dosage of 0.04 g. The pH study shows that ibuprofen adsorption increased with increase in pH from 4 to 10, while removal efficiency decreased at pH 14. Simultaneously, the adsorption isotherm of Langmuir model is best fitted for the adsorption process (R2 = 0.958) on monolayer adsorption. In this study, CaO is identified as an economical, high-efficiency and eco-friendly dormant adsorbent for removal of ibuprofen from aqueous environment.

Management of ibuprofen in wastewater using electrospun nanofibers developed from PET and PS wastes

Electrospinning is a promising technique for the beneficial use and recycling of plastic waste polymers using simple methodologies. In this study, plastic bottles and Styrofoam wastes have been used to develop polyethylene terephthalate (PET) and polystyrene (PS) nanofibers using electrospinning technique separately without any further purification. The effect of the concentration onto the nanofiber's morphology was studied. The fabricated nanofibers were characterized using Field Emission Scanning Electron Microscope (FE-SEM), Fourier Transformed Infrared Spectroscopy (ATR-FTIR), N2 adsorption/desorption analysis, and water contact angle (WCA). Furthermore, the prepared nanofibers were applied for the adsorption of ibuprofen (IBU) from wastewater. Some parameters that can influence the adsorption efficiency of nanofibers such as solution pH, wt.% of prepared nanofibers, drug initial concentration, and contact time were studied and optimized. The results show that the equilibrium adsorption capacity was achieved after only 10 min for 12 wt% PET nanofibers which is equivalent to 364.83 mg/g. For 12 wt% PS nanofibers, an equilibrium adsorption capacity of 328.42 mg/g was achieved in 30 min. The experimental data was fitted to five isotherm and four kinetics models to understand the complicated interaction between the nanofibers and the drug. Langmuir-Freundlich isotherm model showed the best fit for experimental data for both PET and PS nanofibers. The adsorption process was characterized by predominantly physical reaction rather than chemical adsorption for both materials. The reusability study revealed that the synthesized nanofibers maintain their ability to adsorb/desorb IBU for up to five cycles. The results obtained demonstrated that fabricated nanofibers from plastic wastes could perform promising adsorbents for the management of IBU in wastewater. However, further research is needed for the scaling-up the fabrication which is required for real-world applications.

Geopolymer-Based Materials for the Removal of Ibuprofen: A Preliminary Study.

Every year, new compounds contained in consumer products, such as detergents, paints, products for personal hygiene, and drugs for human and veterinary use, are identified in wastewater and are added to the list of molecules that need monitoring. These compounds are indicated with the term emerging contaminants (or Contaminants of Emerging Concern, CECs) since they are potentially dangerous for the environment and human health. To date, among the most widely used methodologies for the removal of CECs from the aquatic environment, adsorption processes play a role of primary importance, as they have proven to be characterized by high removal efficiency, low operating and management costs, and an absence of undesirable by-products. In this paper, the adsorption of ibuprofen (IBU), a nonsteroidal anti-inflammatory drug widely used for treating inflammation or pain, was performed for the first time using two different types of geopolymer-based materials, i.e., a metakaolin-based (GMK) and an organic-inorganic hybrid (GMK-S) geopolymer. The proposed adsorbing matrices are characterized by a low environmental footprint and have been easily obtained as powders or as highly porous filters by direct foaming operated directly into the adsorption column. Preliminary results demonstrated that these materials can be effectively used for the removal of ibuprofen from contaminated water (showing a concentration decrease of IBU up to about 29% in batch, while an IBU removal percentage of about 90% has been reached in continuous), thus suggesting their potential practical application.

UiO-66(Zr) as drug delivery system for non-steroidal anti-inflammatory drugs

The toxicity for the human body of non-steroidal anti-inflammatory drugs (NSAIDs) overdoses is a consequence of their low water solubility, high doses, and facile accessibility to the population. New drug delivery systems (DDS) are necessary to overcome the bioavailability and toxicity related to NSAIDs. In this context, UiO-66(Zr) metal-organic framework (MOF) shows high porosity, stability, and load capacity, thus being a promising DDS. However, the adsorption and release capability for different NSAIDs is scarcely described. In this work, the biocompatible UiO-66(Zr) MOF was used to study the adsorption and release conditions of ibuprofen, naproxen, and diclofenac using a theoretical and experimental approximation. DFT results showed that the MOF-drug interaction was due to an intermolecular hydrogen bond between protons of the groups in the defect sites, (μ3 − OH, and − OH2) and a lone pair of oxygen carboxyl functional group of the NSAIDs. Also, the experimental results suggest that the solvent where the drug is dissolved affects the adsorption process. The adsorption kinetics are similar between the drugs, but the maximum load capacity differs for each drug. The release kinetics assay showed a solvent dependence kinetics whose maximum liberation capacity is affected by the interaction between the drug and the material. Finally, the biological assays show that none of the systems studied are cytotoxic for HMVEC. Additionally, the wound healing assay suggests that the UiO-66(Zr) material has potential application on the wound healing process. However, further studies should be done.

Blending polydopamine-derived imprinted polymers with rice straw-based fluorescent carbon dots for selective detection and adsorptive removal of ibuprofen

Dual-functioning probes capable of detecting and removing hazardous substances have recently received increased attention compared to exclusive sensory probes. Herein, a new composite is synthesized by blending polydopamine imprinted polymers with fluorescent carbon dots (PIP-FCDs) for the selective recognition and adsorption of Ibuprofen (IBF). IBF is a nonsteroidal anti-inflammatory drug and is excessively released in the pharmaceutical wastes. The PIP-FCDs consist of confined pockets for encasing IBF and quenches fluorescence signal when contact with the molecule. PIP-FCDs show high sensitivity (limit of detection = 1.58 × 10−5 μM) and selectivity towards IBF in the presence of other pharmaceutical drugs i.e., aspirin, ketoprofen, norfloxacin, and levofloxacin. The adsorption studies show an adsorption capacity of 209.8 mg g−1 with an extraction efficiency of around 99.9 %. Furthermore, PIP-FCDs are utilized to determine IBF levels in various aqueous pharmaceutical samples. This development provides a simple and dual-functioning probe for the detection and adsorption of IBF from various matrices.

Performance and optimization of diclofenac and ibuprofen adsorption onto activated carbon synthesized from sunflower seed shell (Helianthus annuus) in natural groundwater samples

Performance and optimization of diclofenac and ibuprofen adsorption onto activated carbon synthesized from sunflower seed shell (Helianthus annuus) in natural groundwater samples

Modeling the adsorption of ibuprofen on the Zn-decorated S,P,B co-doped C2N nanosheet: Machine learning and central composite design approaches

The ibuprofen (IB) residuals in water resources are classified as toxic and non-biodegradable contaminants. In the previous study, the Zn-decorated S,P,B co-doped C2N (Zn-SPB@C2N) nanosheet exhibited significant effectiveness in adsorbing IB from aqueous solutions. However, the operating conditions were not optimized for the adsorption process. The current study modeled the adsorption of IB onto Zn-SPB@C2N nanosheets employing central composite design (CCD) and machine learning (ML) methods under various operating conditions. The operating conditions included adsorbent mass, initial IB concentration, and pH. The CCD model revealed a mean squared error (MSE) value of 36.56. The ML investigations showed MSE values of 28.12 for the artificial neural network (ANN), 10.12 for the decision tree (DT), 8.68 for the linear regression (LR), and 3.70 for the random forest (RF) models. The RF model demonstrated high reliability in predicting IB removal across various conditions compared to other methods. Using the RF model, a maximum removal efficiency of 98 % was achieved under the optimized operating conditions, containing a pH of 7, an initial concentration of 59 mg/L, and an adsorbent mass of 0.020 g.

Polyethyleneimine-functionalized magnetic sugarcane bagasse cellulose film for the efficient adsorption of ibuprofen

Polyethyleneimine-modified magnetic sugarcane bagasse cellulose film (P-SBC/Fe3O4 film) was simply fabricated for the removal of ibuprofen (IBP), a typical emerging organic contaminant. The P-SBC/Fe3O4 film exhibited an equilibrium adsorption amount of 370.52 mg/g for IBP and a corresponding removal efficiency of 92.63 % under following adsorption conditions: 318 K, pH 4, and 0.25 mg/mL dosage. Thermodynamic studies indicated that adsorption of IBP on the P-SBC/Fe3O4 film was spontaneous (∆G < 0) and endothermic (∆H > 0). The adsorption data conformed to the Freundlich isotherm model and multilayer adsorption model (two layers), and an average of 3–4 active sites on the P-SBC/Fe3O4 film share an IBP molecule. Both the EDR-IDR and AOAS models vividly described the dynamic characteristics of adsorption process. Model fitting results, theoretical calculations, and comprehensive characterization revealed that adsorption is driven by electrostatic interactions between the primary amine of P-SBC/Fe3O4 film and the carboxyl group of IBP molecule, while other weak interactions are also non-ignorable. Furthermore, quantitative calculations based on density functional theory (DFT) underscored the importance of PEI functionalization. In conclusion, P-SBC/Fe3O4 film is an environmentally friendly and cost-effective adsorbent with significant potential for effectively removing IBP, while maintaining its efficacy over multiple cycles.

Synthesis of Molecularly Imprinted Polymers with Magnetite Cores for Ibuprofen Adsorption

Ibuprofen (IBP) is a pollutant that is widely found in aquatic environments due to pharmaceutical waste and the metabolic results of humans who consume the drug. These compounds can cause damage to aquatic ecosystems, genotoxicity, and aquatic toxicity and are harmful to human health. This study aims to selectively adsorb IBP using magnetic molecularly imprinted polymers (MMIPs) synthesized from ibuprofen (IBP) as a template molecule, methacrylic acid (MAA) as a functional monomer, and divinylbenzene (DVB) as a crosslinker with a mole ratio of 1:4:20 in acetonitrile porogen solvent using a bulk polymerization method. Fe3O4 nanoparticles and MMIPs were characterized using X-ray diffraction (XRD), Fourier Transform Infra-Red (FTIR), and Scanning Electron Microscope (SEM). IBP adsorption reached optimum conditions at pH 3 with a contact time of 90 minutes and a mass of 25 mg of adsorbent. The adsorption performance of MMIPs for IBP was evaluated by adsorption isotherms and adsorption kinetics. Adsorption of IBP by MMIPs followed the Langmuir adsorption isotherm model with an adsorption capacity of 227.24 mg/g. Kinetic studies showed that the adsorption process followed a pseudo-second-order adsorption kinetic model. MMIPs can adsorb IBP selectively even in the presence of interfering compounds, are easily separated from the solution, and can be used repeatedly with good adsorption ability. Hence, it is efficient and promising for removing IBP from aqueous media.