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Herein, we described the use of exfoliated graphene- (EG-) decorated magnetic MnFe2O4 nanocomposite (EG@MnFe2O4) for the removal and adsorption of Congo red (CR) dye from wastewater. Firstly, the precursors (EG, MnFe2O4) and EG@MnFe2O4 were fabricated, characterized using several physical analytical techniques such as X-ray powder diffraction (XRD), scanning electron microscope (SEM), transmission electron microscopy (TEM), and N2adsorption/desorption isotherm measurement. For the adsorption experiments, the effect of contact time (0–240 min), concentration (10–60 mg/L), solution pH (2–10), adsorbent dosage (0.03–0.07 g), and temperature (283–313 K) was rigorously studied. To elucidate the adsorption mechanism and behaviour of CR over EG@MnFe2O4 and MnFe2O4 adsorbents, the kinetic models (pseudo-first-order, pseudo-second-order, Elovich, and Bangham) and isotherm models (Langmuir, Freundlich, Temkin, and Dubinin–Radushkevich) have been adopted. The kinetic results indicated that models adhered to the pseudo-second-order equation, exhibiting the chemisorption mechanism in heterogeneous phrase. Meanwhile, the isotherm results revealed the adsorption of CR over EG@MnFe2O4 obeyed the monolayer behaviour (Langmuir model) rather than multilayer behaviour (Freundlich equation) over MnFe2O4. The thermodynamic study also suggested that such adsorption was an endothermic and spontaneous process. With high maximum adsorption capacity (71.79 mg/g) and good recyclability (at least 4 times), EG@MnFe2O4 can be a potential alternative for the adsorptive removal of CR dye from water. [ABSTRACT FROM AUTHOR]

Chloramphenicol (CAP) is commonly employed in veterinary clinics, but illegal and uncontrollable consumption can result in its potential contamination in environmental soil, and aquatic matrix, and thereby, regenerating microbial resistance, and antibiotic-resistant genes. Adsorption by efficient, and recyclable adsorbents such as mesoporous carbons (MPCs) is commonly regarded as a "green and sustainable" approach. Herein, the MPCs were facilely synthesized via the pyrolysis of the metal–organic framework Fe3O(BDC)3 with calcination temperatures (x °C) between 600 and 900 °C under nitrogen atmosphere. The characterization results pointed out mesoporous carbon matrix (MPC700) coating zero-valent iron particles with high surface area (~225 m2/g). Also, significant investigations including fabrication condition, CAP concentration, effect of pH, dosage, and ionic strength on the absorptive removal of CAP were systematically studied. The optimal conditions consisted of pH = 6, concentration 10 mg/L and dose 0.5 g/L for the highest chloramphenicol removal efficiency at nearly 100% after 4 h. Furthermore, the nonlinear kinetic and isotherm adsorption studies revealed the monolayer adsorption behavior of CAP onto MPC700 and Fe3O(BDC)3 materials via chemisorption, while the thermodynamic studies implied that the adsorption of CAP was a spontaneous process. Finally, adsorption mechanism including H-bonding, electrostatic attraction, π–π interaction, and metal–bridging interaction was proposed to elucidate how chloramphenicol molecules were adsorbed on the surface of materials. With excellent maximum adsorption capacity (96.3 mg/g), high stability, and good recyclability (4 cycles), the MPC700 nanocomposite could be utilized as a promising alternative for decontamination of chloramphenicol antibiotic from wastewater. [ABSTRACT FROM AUTHOR]

Asteraceae presents one of the most globally prevalent, cultivated, and fundamental plant families. However, a large amount of agricultural wastes has been yearly released from Asteraceae crops, causing adverse impacts on the environment. The objective of this work is to have insights into their biomass potentials and technical possibility of conversion into biochars. Physicochemical properties are systematically articulated to orientate environmental application, soil amendment, and other utilizations. Utilizations of Asteraceae biochars in wastewater treatment can be categorized by heavy metal ions, organic dyes, antibiotics, persistent organic pollutants (POPs), and explosive compounds. Some efforts were made to analyze the production cost, as well as the challenges and prospects of Asteraceae-based biochars., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier B.V. All rights reserved.)

The potential of green nanomaterials for environmental and agricultural fields is emerging due to their biocompatible, eco-friendly, and cost-effective performance. We report the use of Canna indica flowers extract as new capping and stabilizing source to bio-fabricate ZnO nanoparticles (ZnO NPs for dyes removal, seed germination. ZnO NPs was biosynthesized by ultrasound-assisted alkaline-free route to reach the critical green strategy. The physicochemical findings of ZnO revealed small crystallite size (27.82 nm), sufficient band-gap energy (3.08 eV), and diverse functional groups. Minimum‑run resolution IV approach found the most pivotal factors influencing on removal of Coomassie Brilliant Blue G-250. Uptake studies pointed out that pseudo second-order, and Langmuir were the best fitted models. Dye molecules behaved monolayer adsorption on ZnO surface layers, and controlled by chemisorption. Natural solar light was used as effective source for photocatalytic degradation of methylene blue (94.23% of removal and 31.09 mg/g of uptake capacity). Compared with H 2 O and ZnSO 4 , ZnO NPs positively affected the growth of shoot and root lengths (10.2-27.8%) of bean seedlings in most cases. ZnO acts an agrochemical for boosting weight gain, and germination ratio. This study may be promising for developing the recyclable, multifunctional ZnO nanoparticles for environmental and agricultural applications., (Copyright © 2021 Elsevier B.V. All rights reserved.)

Aquatic contamination of diclofenac (DCF), an emergent non-steroidal anti-inflammatory drug (NSAIDs), can result in adverse effects to many ecosystems through biomagnification. Hence, introducing effective remediation techniques to sequester the pharmaceutical wastes is highly fundamental to prevent their accumulation in the environment. Generally, adsorption has been presented as a green and efficient approach. Herein, we report the characterization and application of the novel magnetic nanocomposite (GO@CoFe 2 O 4 ) derived from cobalt-based ferrite (CoFe 2 O 4 ) and graphene oxide (GO) for DCF adsorption. For the optimization procedure, the response surface methodology (RSM) was adopted to investigate the impacts of DCF concentration (1.6-18.4 mg/L), DCF dosage (0.08-0.92 g/L), and solution pH (2.6-9.4) to find the optimum conditions for DCF removal, at 10.5 mg/L, 0.74 g/L, and pH 4, respectively. For the adsorption experiments, the kinetic, isotherm, thermodynamic, and intraparticle diffusion models were systematically studied. Moreover, we have elucidated the role of functional groups on the surface of GO@CoFe 2 O 4 in enhancing the adsorption of DCF drug. With good removal efficiency (up to 86.1%), high maximum adsorption capacity (32.4 mg/g), GO@CoFe 2 O 4 can be a potential candidate to eliminate DCF drug from water., (Copyright © 2020. Published by Elsevier B.V.)

Herein, a facile strategy to fabricate the novel manganese oxide-imprinted mesoporous carbons (MOPCx, x presents for pyrolysis temperature) was described via the direct pyrolysis of Mn 2 (BDC) 2 (DMF) 2 (BDC = 1,4-benzenedicarboxylate, DMF = N,N-dimethylformamide) as a self-sacrificed template at various temperatures (x = 550, 750, and 950  ° C). The characterization results demonstrated the existence of MnO embedded in carbon structures with different morphologies, and enhancing surface areas (249.86-294.67 m 2 /g) compared with their precursor (3.59 m 2 /g). For methylene blue adsorption experiments, the MOPC pyrolyzed at 950  ° C (MOPC950) revealed the best candidate with maximum uptake capacity (124.1 mg/g), so far higher than other MOPCx and Mn 2 (BDC) 2 (DMF) 2 materials. Finally, adsorption mechanisms involving H-bond, and π-π interaction were proposed via the chemisorption between surface functional groups (carboxyl, phenol, lactone, and base)., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

In this study, a minimum-run resolution IV and central composite design have been developed to optimize tetracycline removal efficiency over mesoporous carbon derived from the metal-organic framework MIL-53 (Fe) as a self-sacrificial template. Firstly, minimum-run resolution IV, powered by the Design-Expert program, was used as an efficient and reliable screening study for investigating a set of seven factors, these were: tetracycline concentration (A: 5-15 mg/g), dose of mesoporous carbons (MPC) (B: 0.05-0.15 g/L), initial pH level (C: 2-10), contact time (D: 1-3 h), temperature (E: 20-40 °C), shaking speed (F: 150-250 rpm), and Na + ionic strength (G: 10-90 mM) at both low (-1) and high (+1) levels, for investigation of the data ranges. The 20-trial model was analyzed and assessed by Analysis of Variance (ANOVA) data, and diagnostic plots (e.g., the Pareto chart, and half-normal and normal probability plots). Based on minimum-run resolution IV, three factors, including tetracycline concentration (A), dose of MPC (B), and initial pH (C), were selected to carry out the optimization study using a central composite design. The proposed quadratic model was found to be statistically significant at the 95% confidence level due to a low P -value (<0.05), high R 2 (0.9078), and the AP ratio (11.4), along with an abundance of diagnostic plots (3D response surfaces, Cook's distance, Box-Cox, DFFITS, Leverage versus run, residuals versus runs, and actual versus predicted). Under response surface methodology-optimized conditions (e.g., tetracycline concentration of 1.9 mg/g, MPC dose of 0.15 g/L, and pH level of 3.9), the highest tetracycline removal efficiency via confirmation tests reached up to 98.0%-99.7%. Also, kinetic intraparticle diffusion and isotherm models were systematically studied to interpret how tetracycline molecules were absorbed on an MPC structure. In particular, the adsorption mechanisms including "electrostatic attraction" and "π-π interaction" were proposed.