Search

Objectives: The closure integrity and process validation of closed system transfer devices (CSTDs) should be confirmed before implementation in clinical settings. We aimed to investigate the closure integrity and validate the aseptic procedure of two types of CSTDs by using a combination of the dye ingress test and a media fill test., Methods: The dye ingress test with methylene blue was used for both CSTDs with 10 samples of drug vials of three brands. A media fill test was performed with both CSTDs (300 samples per CSTD, 150 carried out in a safety cabinet and 150 under non-classified environmental conditions)., Results: In all samples of both CSTDs, methylene blue was absent after visual inspection and spectrophotometric analysis. The nutrient media of one sample with CSTD A and none of the CSTD B samples were contaminated when reconstituted in a GMP grade A environment. Under non-classified environmental conditions, one sample of CSTD A and two samples of CSTD B were contaminated., Conclusions: Both CSTDs connected to the drug vials met the terms of closure integrity by using the dye ingress test. The aseptic procedure of CSTD B was validated with the media fill test when reconstituted in a GMP grade A environment, but failed for CSTD A. Both CSTDs failed the media fill test when reconstituted under non-classified environmental conditions., Competing Interests: Competing interests: None declared., (© European Association of Hospital Pharmacists 2024. No commercial re-use. See rights and permissions. Published by BMJ.)

In this study, three acid mine drainage (AMD) sources were investigated as potential sources of iron for the synthesis of iron nanoparticles using green tea extract (an environmentally friendly reductant) or sodium borohydride (a chemical reductant). Electrical conductivity (EC), total dissolved solids (TDS), dissolved oxygen (DO), oxidation-reduction potential (ORP), ion chromatography (IC), and inductively coupled plasma-mass spectroscopy (ICP-MS) techniques were used to characterize the AMD, and the most suitable AMD sample was selected based on availability. Additionally, three tea extracts were characterized using ferric-reducing antioxidant power (FRAP) and 2,2-diphenyl-1-picryl-hydrazine-hydrate (DPPH), and the most suitable environmentally friendly reductant was selected based on the highest FRAP (1152 µmol FeII/g) and DPPH (71%) values. The synthesized iron nanoparticles were characterized and compared using XRD, STEM, Image J, EDS, and FTIR analytical techniques. The study shows that the novel iron nanoparticles produced using the selected green tea (57 nm) and AMD were stable under air due to the surface modification by polyphenols contained in green tea extract, whereas the nanoparticles produced using sodium borohydride (67 nm) were unstable under air and produced a toxic supernatant. Both the AMD-based iron nanoparticles can be used as Fenton-like catalysts for the decoloration of methylene blue solution. While 99% decoloration was achieved by the borohydride-synthesized nanoparticles, 81% decoloration was achieved using green tea-synthesized nanoparticles., (© 2024. The Author(s).)

In this investigation, microwave irradiation assisted by ZnCl 2 was used to transform pineapple crown (PN) waste into mesoporous activated carbon (PNAC). Complementary techniques were employed to examine the physicochemical characteristics of PNAC, including BET, FTIR, SEM-EDX, XRD, and pH at the point-of-zero-charge (pH pzc ). PNAC is mesoporous adsorbent with a surface area of 1070 m 2 /g. The statistical optimization for the adsorption process of two model cationic dyes (methylene blue: MB and, crystal violet: CV) was conducted using the response surface methodology-Box-Behnken design (RSM-BBD). The parameters include solution pH (4-10), contact time (2-12) min, and PNAC dosage (0.02-0.1 g/100 mL). The Freundlich and Langmuir models adequately described the dye adsorption isotherm results for the MB and CV systems, whereas the pseudo-second order kinetic model accounted for the time dependent adsorption results. The maximum adsorption capacity ( q max ) for PNAC with the two tested dyes are listed: 263.9 mg/g for CV and 274.8 mg/g for MB. The unique adsorption mechanism of MB and CV dyes by PNAC implicates multiple contributions to the adsorption process such as pore filling, electrostatic forces, H-bonding, and π-π interactions. This study illustrates the possibility of transforming PN into activated carbon (PNAC) with the potential to remove two cationic dyes from aqueous media.

In this study, the manganese oxide/biochar composites (Mn@BC) were synthesized from Phytolacca acinosa Roxb. The Mn@BC was analyzed via techniques of Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and X-ray diffraction analysis (XRD). The results show that MnO x is successfully loaded on the surface of BC, and the load of MnO x can increase the number of surface functional groups of BC. X-ray photoelectron spectroscopy (XPS) shows that MnO x loaded on BC mainly exists in three valence forms: Mn(Ⅱ), Mn(Ⅲ), and Mn(Ⅳ). The ability of Mn@BC to activate periodate (PI) was studied by simulating the degradation of methylene blue (MB) dye. The degradation experiment results showed that the MB removal rate by the Mn@BC/PI system reached 97.4% within 30 min. The quenching experiment and electron paramagnetic resonance (EPR) analysis confirmed that Mn@BC can activate PI to produce iodate (IO 3 •), singlet oxygen ( 1 O 2 ), and hydroxyl radical (•OH), which can degrade MB during the reaction. Response surface methodology (RSM) based on Box-Behnken Design (BBD) was used to determine the interaction between pH, Mn@BC and PI concentration in the Mn@BC/PI system, and the optimum technological parameters were determined. When pH = 5.4, Mn@BC concentration 0.56 mg/L, PI concentration 1.1 mmol/L, MB removal rate can reach 98.05%. The cyclic experiments show that Mn@BC can be reused. After four consecutive runs, the removal rate of MB by the Mn@BC/PI system is still 82%, and the Mn@BC/PI system also shows high performance in treating MB in actual water bodies and degrading other pollutants. This study provides a practical method for degrading dyes in natural sewage., 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 © 2023 Elsevier Inc. All rights reserved.)

In this study, bamboo waste (BW) was subjected to pyrolysis-assisted ZnCl 2 activation to produce mesoporous activated carbon (BW-AC), which was then evaluated for its ability to remove cationic dyes, specifically methylene blue (MB) and crystal violet (CV), from aqueous environments. The properties of BW-AC were characterized using various techniques, including potentiometric-based point of zero charge (pH pzc ), scanning electron microscopy with energy dispersive X-rays (SEM-EDX), X-ray diffraction (XRD), gas adsorption with Brunauer-Emmett-Teller (BET) analysis, infrared (IR) spectroscopy. To optimize the adsorption characteristics (BW-AC dosage, pH, and contact time) of PBW, a Box-Behnken design (BBD) was employed. The BW-AC dose of 0.05 g, solution pH of 10, and time of 8 min are identified as optimal operational conditions for achieving maximum CV (89.8%) and MB (96.3%) adsorption according to the BBD model. The dye removal kinetics for CV and MB are described by the pseudo-second-order model. The dye adsorption isotherms revealed that adsorption of CV and MB onto BW-AC follow the Freundlich model. The maximum dye adsorption capacities ( q max ) of BW-AC for CV (530 mg/g) and MB (520 mg/g) are favorable, along with the thermodynamics of the adsorption process, which is characterized as endothermic and spontaneous. The adsorption mechanism of CV and MB dyes by BW-AC was attributed to multiple contributions: hydrogen bonding, electrostatic forces, π-π attraction, and pore filling. The findings of this study highlight the potential of BW-AC as an effective adsorbent in wastewater treatment applications, contributing to the overall goal of mitigating the environmental impact of cationic dyes and ensuring the quality of water resources.

The seeds of Annona glabra L., an invasive plant in Vietnam, were first employed as a new biosorbent for the adsorption of methylene blue (MB) from aqueous media. The characterizations of the material using FT-IR, SEM, nitrogen adsorption-desorption analysis, and point of zero charge reveals that it possesses a rough and irregular surface, various polar functional groups, and pH pzc of 5.5. Certain adsorption conditions including adsorbent dose, solution pH, contact time, and initial concentration of MB were found to affect adsorption efficiency. The kinetic data are well fitted with pseudo-second-order model with the adsorption rate of 0.002 g mg -1  min -1 and initial rate of 4.46 mg g -1  min -1 . For the adsorption isotherm, three nonlinear models were used to analyze the experiment data, including Langmuir, Freundlich, and Temkin. The results indicate that the Langmuir model best describes the adsorption of Annona glabra L. seeds powder (AGSP) with a maximum adsorption capacity of 98.0 mg g -1 . The investigation underpins the adsorption mechanism, whereby the electrostatic attraction between positively charged MB and negatively charged surface of AGSP is expected to be the predominant mechanism, together with hydrogen bonding and pi-pi interaction. These results make AGSP an interesting biosorbent concerning its environmental friendliness, cost-effectiveness, and relatively high dye adsorption capacity., (© 2023. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)

Improving the convenience, sensitivity, and cost-effectiveness of electrochemical biosensors is crucial for advancing their clinical diagnostic applications. Herein, we presented an elegant approach to construct electrochemical aptasensors for tumor-derived exosome detection by harnessing the alterable interaction between methylene blue (MB) and DNA aptamer. In detail, the anti-EpCAM aptamer, named SYL3C, was found to exhibit a strong affinity toward MB due to the specific interaction between MB and unbound guanine bases. Thereby, SYL3C could be stained with MB to arouse a strong electrochemical signal on a gold electrode (AuE). Upon binding to EpCAM-positive exosomes, SYL3C underwent a conformational transformation. The resulting conformation, or exosomes-SYL3C complex, not only reduced the accumulation of MB on SYL3C by obstructing the accessibility of guanines to MB but also impeded the transfer of electrons from the bound MB to AuE, leading to a notable decrease in the electrochemical signal. Using MB-stained SYL3C as an electronic switch, an electrochemical aptasensor was readily established for the detection of EpCAM-positive exosome detection. Without the need for signal amplification strategies, expensive auxiliary reagents, and complex operation, this unique signal transduction mechanism alone could endow the aptasensor with ultrahigh sensitivity. A limit of detection (LOD) of 234 particles mL -1 was achieved, surpassing the performance of most reported methods. As a proof of concept, the aptasensor was applied to analyze clinical serum samples and effectively distinguish non-small-cell lung cancer (NSCLC) patients from healthy individuals. As EpCAM exhibits broad expression in exosomes derived from different tumor sources, the developed aptasensor holds promise for diagnosing other tumor types.

In the current study, an attempt was made to synthesize coffee husk (CH) activated carbon by chemical modification approach (sulphuric acid-activated CH (SACH) activated carbon) and was used as a valuable and economical sorbent for plausible remediation of Methylene blue (MB) dye. Batch mode trials were carried out by carefully varying the batch experimental variables: SACH activated carbon (SACH AC) dosage, pH, initial dye concentration, temperature, and contact time. The optimum equilibrium time for adsorption by SACH activated carbon was obtained as 60 min, and the maximum adsorption took place at 30 °C. Morphological and elemental composition, crystallinity behaviour, functional groups, and thermal stability were examined using SEM with EDX, XRD, FTIR, BET, TGA, and DTA and these tests showed successful production of activated carbon. The outcomes showed that chemical activation enhanced the number of pores and roughness which possibly maximized the adsorptive potential of coffee husk. The Box-Benken design (BBD) was used to optimize the MB dye adsorption studies and 99.48% MB dye removed at SACH AC dosage of 4.83 g/L at 30 °C for 60 min and pH 8.12, and the maximum adsorption was yielded for sulphuric acid-activated coffee husk carbon carbon with 88.1 mg/g maximum MB adsorption capacity. Langmuir- Freundlich model deliberately provided a better fit to the equilibrium data. The SACH AC-MB dye system kinetics showed a high goodness-of-fit with pseudo second order model, compared to other studied models. Change in Gibbs's free energy (ΔG o ) of the system indicated spontaneity whereas low entropy value (ΔS o ) suggested that the removal of MB dye on the SACH activated carbon was an enthalpy-driven process. The exothermic nature of the sorption cycle was affirmed by the negative enthalpy value (ΔH o ). The adsorptive-desorptive studies reveal that SACH AC could be restored with the maximum adsorption efficiency being conserved after the fifth cycles. Overall, the outcomes revealed that sulphuric acid-activated coffee husk activated carbon (SACH AC) can be used as prompt alternative for low-cost sorbent for treating dye-laden synthetic wastewaters., 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 © 2023 Elsevier Inc. All rights reserved.)

Sugar molasses from agricultural waste could be a sustainable carbon source for the synthesis of graphene adsorbent introduced in this work. The sugar molasses was successfully converted to graphene-like material and subsequently coated on the sand as graphene sand composite (GSC), as proven by XRD, XPS, Raman spectroscopy, and SEM with EDX mapping analyses. The adsorption performance of GSC was evaluated against the removal of Tetracycline (TC) and methylene blue (MB) pollutants from an aqueous solution in a fixed bed column continuous-flow adsorption setup. The effect of different process conditions: bed height (4-12 cm), influent flow rate (3-7 mL/min), and contaminants' concentration (50-150 ppm) was investigated. The results revealed that column performance was improved by increasing the bed depth and lowering the flow rate and concentration of the pollutants. The best removal efficiency was obtained when the bed height was 12 cm, the influent flow rate of 3 mL/min, and the pollutants' initial concentration was 50 mg/L. Thomas, Adams-Bohart, and Yoon-Nelson models were attempted to fit the breakthrough curves. Regeneration of the GSC indicated the decline of breakthrough time from 240-280 to 180 min, reflecting the decrease in adsorptive sites due to the incomplete regeneration process. Overall, sugar molasses was shown to be a low-cost precursor for synthesizing valuable graphene material in the form of GSC, which can reduce the problem for industrial waste management of sugar molasses, and the GSC could be used as an adsorbent for environmental application., (© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

A novel gas-liquid hybrid double dielectric barrier discharge (DDBD) reactor with coaxial cylinder configuration was developed for the degradation of methylene blue (MB) in this study. In this DDBD reactor, the reactive species generation occurred in the gas-phase discharge, directly in the liquid, and in the mixture of the working gas bubbles and the liquid, which could effectively increase the contact area between the active substance and MB molecules/intermediates, resulting in an excellent MB degradation efficiency and mineralization (COD and TOC). The electrostatic field simulation analysis by Comsol was carried out to determine the appropriate structural parameters of the DDBD reactor. The effect of discharge voltage, air flow rate, pH, and initial concentration on MB degradation was evaluated. Besides, major oxide species, ·OH, the dissolved O 3 and H 2 O 2 generated in this DDBD reactor were determined. Moreover, major MB degradation intermediates were identified by LC-MS, based on which, possible degradation pathways of MB were proposed., 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 © 2023. Published by Elsevier Ltd.)

Nanoparticle synthesis from plant resources has recently gained significant impact due to its low cost, simple equipment requirements, and ease of availability. In this work, DR-AgNPs were synthesized using bark extract of Delonix regia (D. regia) plant under microwave irradiation. The formation of DR-AgNPs has been confirmed with UV-Vis, XRD, FTIR, FESEM, HRTEM, EDS, DLS, and zeta potential analysis. Catalytic and antioxidant activities were tested on synthesized spherical nanoparticles with a size range of 10-48 nm. The effects of pH and catalyst dosage on the methylene blue (MB) dye degradation were carried out. It was observed from the treatment results that 95% MB dye degradation efficiency was achieved within 4 min with a degradation rate constant of 0.772 min -1 . The synthesized nanoparticles showed a strong antioxidant property when analyzed by a 2,2-Diphenyl-1-picrylhydrazyl (DPPH) radical scavenging assay. The calculated IC 50 value for DR-AgNPs was 37.1 ± 0.12 μg mL -1 . Therefore, DR-AgNPs are excellent in both catalytic and antioxidant activities when compared to previously reported works. HIGHLIGHTS: Green synthesis of silver nanoparticles (DR-AgNPs) using Delonix regia bark extract. The catalytic activity of DR-AgNPs is remarkable against Methylene Blue. DR-AgNPs also have a strong DPPH radical antioxidant effect. Short degradation time, high degradation rate constant, and a good scavenging activity are key features of this study compared to previously reported works., (© 2023 Wiley Periodicals LLC.)

The complexity of the chemistry behind the hydrothermal conversion is enormous. Components interact with their own physical and chemical structure, making it harsh to understand the conversion as a whole. Herein, the six-water recirculation and loading nano SiO 2 experiment in a one-pot hydrothermal carbonization procedure was designed to elucidate the mechanism of regulating the functional groups and microporous structure of the hydrochar surface. The hydrochar prepared by the second circulating liquid and loading nano-SiO 2 (HBC-R2/Si) was equipped most enriched functional groups (carboxyl = 11.48 μmol/g, phenolic hydroxyl = 52.98 μmol/g, lactone groups = 46.52 μmol/g) and suitable pore size (1.90 nm-1.93 nm) as a sorbent riched in hemicellulose. The sorption kinetics (equilibrium reached ≈ 480 min) are approximately evenly fitted by the pseudo-second-order, Weber and Morris, and Elovich models, indicating that membranes and particles diffusion, pore diffusion, and surface sorption coexisted in the sorption of methylene blue (MB) on the hydrochar materials. Simultaneously, all hydrochar materials achieved over 25% MB removal within 90 min (liquid membrane diffusion) and over 40% for HBC-R2 and HBC-R2/Si, suggesting that liquid membrane diffusion is the predominant rate-limiting step. Pearson's correlation analysis and Mantel's analysis announced that the cation exchange capacity (CEC), pore size, and carboxyl groups on the hemicellulose affect the sorption capacity by limiting the pore diffusion procedure. However, the CEC and the phenolic hydroxyl groups on the cellulose and hemicellulose affect the sorption rate by limiting membrane diffusion. Three consecutive sorption/desorption cycles confirmed the high stability and reusability of HBC-R2/Si composites., 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 © 2023 Elsevier Inc. All rights reserved.)

Hydrochars are promising sorbents for wastewater treatment. Herein, two acrylate-modified hydrochars (AMHC 1 and AMHC 2 ) were obtained by grafting acrylic acid on the surface of two hydrochars (MHC 1 and MHC 2 hydrothermally carbonized in water and acidic medium respectively) with free radical polymerization. Characterizations show that MHC 2 is more prone to free radical polymerization than MHC 1 does, and has higher carboxylate content after modification. The adsorption amounts of AMHC 2 over methylene blue (MB) and Pb(II) are much higher than those of AMHC 1 . Pseudo-second-order kinetic and Langmuir isotherm equations well fit the Pb(II) and MB sorption data of AMHC 2 . The Pb(II) adsorptive mechanism is mainly inner-surface complexation accompanied by ion exchange and cation-π interaction. MB adsorption involves ion exchange, electrostatic interaction, H-bonding and π-π interaction. Hence, the one-step modification method of free radical polymerization under alkaline condition has great potential for preparing carboxylate-modified hydrochars to adsorb cationic pollutants., 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 © 2023 Elsevier Ltd. All rights reserved.)

An itaconate-functionalized hydrochar (IFHC) was prepared from one-step solvent-free radical copolymerization of bamboo hydrochar, itaconic acid, ammonium persulphate and sodium hydroxide in solvent-free environment, and was employed to absorb methylene blue (MB) and Pb(II) from wastewater. Characterizations show IFHC has rich carboxylate and tends to adsorb cationic contaminants. The largest adsorbed quantities of MB and Pb(II) by IFHC are up to 1036 and 291.8 mg·g -1 at 298 K respectively as per the Langmuir isotherm. Sorption of MB and Pb(II) onto IFHC can be expressed well by Langmuir isotherm and pseudo-2nd-order kinetics equations. The high sorption performance depends on the rich carboxylate, which can adsorb MB/Pb(II) through an electrostatic interaction/inner-surface complexation mechanism. The sorptive capacity of regenerated IFHC decreased below 10% after 5 desorption-resorption cycles. Thus, the solvent-free free radical copolymerization is an environmentally-friendly strategy to synthesize novel efficient sorbents that can clean cationic contaminants from wastewater., 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 © 2023 Elsevier Ltd. All rights reserved.)

The copolymer beads prepared by suspension polymerisation were decorated with MnO 2 nanoparticles and successfully implemented for the efficient removal of toxic organic contaminants from water. Copolymer-MnO 2 nanocomposite was further analysed using XRD, SEM and optical microscope. The SEM images showed the surface characteristics of MnO 2 nanoparticles on copolymer beads. The efficiency of the copolymer-MnO 2 nanocomposite for the removal of model pollutant methylene blue and rhodamine B is then analysed by changing the concentration of pollutant. The results obtained exhibited 18.45 mg/g for methylene blue adsorption and 3.125 mg/g for rhodamine B. The adsorption equilibrium results were fitted to Langmuir adsorption isotherm for both methylene blue and rhodamine B adsorption. The desorption studies were performed for five consecutive cycles, and material was showing good regenerating capacity towards both organic pollutants. The obtained results show that copolymer-MnO 2 nanocomposite is an efficient material for the removal of organic contaminants from wastewater., (© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

A new, simple and sensitive method for determining and confirming methylene blue and its analogues such as azure A, azure B, azure C, thionine, and new methylene blue in fish muscles have been developed. The method is based on acetonitrile extraction followed by extract purification using dispersive solid-phase extraction (dSPE) with basic aluminium oxide (ALN) and solid-phase extraction (SPE) using primary and secondary amines (PSA) sorbent in matrix adsorption mode. The separation and detection of the dyes in the fish extract are achieved within 5 min by ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) using an octadecyl analytical column with a mixture of acetonitrile, methanol and 0.1% formic acid as a mobile phase in gradient elution. The developed method has been in-house validated according to European law. The method recovery for fish muscle was 98.3-103.1%, whereas the decision limit (CCα) was from 0.45 to 0.49 µg kg -1 .

Alkaline leachate, dust generation, and foul smell during the stacking process of natural rubber biosludge (NRBS) can pollute surrounding water, soil, and air. In this study, natural rubber chemically activated carbon (NRCAC) has been synthesized for the first time from NRBS by pyrolysis using ZnCl 2 at 700 °C for adsorptive removal of Cr(VI) and methylene blue (MB) from aqueous solutions. Both NRBS and NRCAC were characterized by X-ray fluorescence (XRF), X-ray diffraction (XRD), Fourier transform infrared (FTIR), scanning electron microscopy-energy dispersive spectroscopy (SEM-EDS), Brunauer-Emmett-Teller (BET), and thermogravimetric analyzer (TGA). FTIR and SEM-EDS suggested significant functional and morphological transformations in NRCAC. Experimental investigations of different process parameters, such as pH, concentration, contact time, salt concentration, etc., were conducted to study their influences on adsorption. Adsorption and desorption kinetics followed a pseudo-second-order model, while adsorption equilibrium followed Liu isotherm. Maximum uptake calculated from the Liu model was 81.28 and 211.90 mg/g for Cr(VI) and MB, respectively. Thermodynamic analysis established spontaneous and endothermic adsorption. Up to five adsorption/desorption cycles were conducted using eluents such as 1 M NaOH and water for Cr(VI) and MB, respectively. Electrostatic attraction and ion-exchange favored Cr(VI)/MB adsorption, while hydrogen bonding and π-π stacking were significant in MB uptake. Overall findings suggest that NRBS (a renewable agro-industrial, abundant, and freely available) could be employed to synthesize biochar for adsorptive removal of wastewater containing Cr(VI)/MB.

Herein, tropical fruit biomass wastes including durian seeds (DS) and rambutan peels (RP) were used as sustainable precursors for preparing activated carbon (DSRPAC) using microwave-induced H 3 PO 4 activation. The textural and physicochemical characteristics of DSRPAC were investigated by N 2 adsorption-desorption isotherms, X-ray diffraction, Fourier transform infrared, point of zero charge, and scanning electron microscope analyses. These findings reveal that the DSRPAC has a mean pore diameter of 3.79 nm and a specific surface area of 104.2 m 2 /g. DSRPAC was applied as a green adsorbent to extensively investigate the removal of an organic dye (methylene blue, MB) from aqueous solutions. The response surface methodology Box-Behnken design (RSM-BBD) was used to evaluate the vital adsorption characteristics, which included (A) DSRPAC dosage (0.02-0.12 g/L), (B) pH (4-10), and (C) time (10-70 min). The BBD model specified that the DSRPAC dosage (0.12 g/L), pH (10), and time (40 min) parameters caused the largest removal of MB (82.1%). The adsorption isotherm findings reveal that MB adsorption pursues the Freundlich model, whereas the kinetic data can be well described by the pseudo-first-order and pseudo-second-order models. DSRPAC exhibited good MB adsorption capability (118.5 mg/g). Several mechanisms control MB adsorption by the DSRPAC, including electrostatic forces, π-π stacking, and H-bonding. This work shows that DSRPAC derived from DS and RP could serve as a viable adsorbent for the treatment of industrial effluents containing organic dye.

The present work explores the sorption performance of Sterculia foetida pod (SFP) for the removal of methylene blue (MB) and chromium (Cr 6+ ) from simulated solutions separately. The material characteristics namely textural analysis (specific surface area: 2.45 m 2 /g), morphological behavior (heterogeneous morphology containing pores and cavities), functional analysis (COO- stretching, C-O-C stretching vibrations, and -OH stretching) and thermal behavior (279.4 °C) were examined by various analytical techniques namely BET, SEM, FTIR, and TGA. Using non-linear Langmuir isotherm analysis, the maximal sorption capacity of SFP for the removal of MB and Cr 6+ was predicted to be 74.1 mg/g and 27.3 mg/g, respectively. The optimized condition for sorption of MB and Cr 6+ onto SFP was: dosage: 0.07 mg/L, initial pH: 7 (MB), and 2 (Cr 6+ ). Thermodynamic data analysis confirmed the endothermic, favorable, spontaneous, and physisorption nature of sorption. The SFP has shown significant regeneration capacity in the consecutive runs (MB: 92.5% removal till 5th trial; Cr 6+ : 97.6% removal till 3rd trial). Based on these findings, SFP is a promising low-cost and eco-friendly candidate for the removal of anionic and cationic toxic pollutants in the absence of energy and chemical expenditure.NOVELTY STATEMENT Sterculia foetida pod (SFP) explored for the removal of anionic and cationic toxic pollutants in the absence of energy and chemical expenditure.Mechanism for the interaction between toxic pollutants and SFP was predicted.Better sorption capacity (MB: 74.1 mg/g; Cr 6+ : 27.8 mg/g) and better regeneration capacity (MB: 92.5% for 5th trial; Cr 6+ : 97.6% for 3rd trial) was achieved.A feasible and spontaneous nature of sorption process toward the removal of MB and Cr 6+ was demonstrated using thermodynamic relations.

This study evaluated the characteristics of zinc chloride modified vitex doniana seed activated carbon (VDZnCl2) for the removal of methylene blue. VDZnCl2 was characterized for textural properties, surface morphology and surface chemistry. Batch adsorption of methylene blue by VDZnCl2 was evaluated for the effects of concentration, contact time, adsorbent dosage, and solution pH. The surface area increased from 14 to 933 m 2 /g with porous texture to facilitate adsorption. The SEM micrograph showed varieties of pores with widened cavities. The FTIR spectra showed the characteristics of O-H and C=C groups commonly found in carbonaceous materials. The maximum methylene blue adsorption was recorded as 238 mg/g at concentration range of 1-800 mg/L and VDZnCl2 dosage of 50 mg. Sips isotherm fitted well with the equilibrium data, suggesting that the adsorption by VDZnCl2 was a physical process onto its heterogeneous surface, while the applicability of pseudo-first-order kinetics implies that external diffusion was the rate controlling mechanism. The performance put up by VDZnCl2 suggested that it is a potential adsorbent substitute for dye wastewater treatment.

Ligno-cellulosic biomasses had been recognized for their potential use to produce chemicals and biomaterials. The current study focused on the use of a new cellulosic Robinia Pseudoacacia fiber and extracted lignin as adsorbents for methylene blue (a cationic dye). The biomaterials were analyzed using FT-IR spectroscopy, SEM, XRD, and TGA-DTA techniques. The surface of Robinia fibers was rough and porous. The crystallinity index (CrI) value for Robinia fibers was found to be 32%. The ability of the studied samples to remove methylene blue from water was assessed under the variation of time, pH, dye concentration, temperature, and NaCl concentration. The maximum adsorption capacity of methylene blue reached 191 mg/g for Robinia fibers and it achieved 22 mg/g for the extracted lignin ( T  = 20 °C, pH = 6, and time = 90 min). The adsorption data complied with the pseudo second-order kinetic model and both Langmuir and Freundlich isotherms. Based on these findings, the process suggested the occurrence of many physicochemical interactions between methylene blue molecules and the studied biomaterials. The adsorption mechanism was exothermic, non-spontaneous, and it was described by the decrease of the disorder. Adsorption results proved that Robinia fiber was an attractive candidate for the removal of cationic dyes from water.

In this study, Mango ( Mangifera indica ) seeds (MS) and peels (MP) seeds mixed fruit wastes were employed as a renewable precursor to synthesize high-surface-area-activated carbon (MSMPAC) by using microwave-induced ZnCl 2 activation. Thus, the applicability of MSMPAC was evaluated towards the removal of cationic dye (methylene blue, MB) from an aqueous environment. The key adsorption factors, namely A: MSMPAC dose (0.02-0.1 g), B: pH (4-10), and C: time (5-15 min), were inspected using the desirability function of the Box-Behnken design (BBD). Thus, the adsorption isotherm data were found to correspond well with the Langmuir model with a maximum adsorption capacity of (232.8 mg/g). Moreover, the adsorption kinetics were consistent with both pseudo-first-order and pseudo-second-order models. The spontaneous and endothermic nature of MB adsorption on the MSMPAC surface could be inferred from the negative ∆G° values and positive value of ∆H°, respectively. Various mechanisms namely electrostatic forces, pore filling, π-π stacking, and H-bonding govern MB adsorption by the MSMPAC. This study demonstrates the utility of MS and MP as renewable precursors to produce high-surface area MSMPAC with a potential application towards the removal of cationic organic dyes such as MB.

This research emphasizes the performance of some eco-friendly carbon materials as hydrochars (HC) obtained by the hydrothermal carbonization (HTC) process applied to walnut shell (WS) biowaste. These materials display promising properties that can be used for environmental applications such as emerging pharmaceutical pollutant retention from water sources. Thus, three hydrochars coded HCWS1, HCWS2, and HCWS3 were obtained using a dynamic autoclave in specific conditions-temperature of 220 °C, autogenous pressure, 1:10 biomass-water weight ratio-and for three different reaction times, 1 h, 6 h, and 12 h. The HCWSs were characterized by means of ATR-FTIR and SEM-EDS analyses and tested as possible adsorbents to assess the removal efficiencies of some emerging pharmaceutical pollutants (paracetamol and methylene blue) by UV-VIS spectrophotometry. Kinetic and adsorption studies were carried out. The best results were obtained for the HCWS3 hydrochar. Further perspectives include an activation step of the hydrochars and their testing on other emerging pharmaceutical pollutants.

In current study, different feeding levels of Moringa oleifera formulated diet was compared to analyze the growth performance, feed conversion ratio, feed conversion efficiency and gut microbiology of Oreochromis niloticus. The study was comprised of four treatment groups including 4%, 8% and 12% Moringa oleifera and one control group which was devoid of Moringa leaves. The experimental trial was conducted at the Zoology laboratory of Pakistan Institute of Applied and Social Sciences, (PIASS) Kasur. The physicochemical parameters of water such as temperature, dissolve oxygen, pH, total dissolved solids and salinity in all aquaria were found non-significantly different from each other. In control condition T1, the average weight gain was 14.89±16.90a grams, while average length gain was 11.52±7.444a cm. However, the total viable count on Eosin methylene blue was 7.4×107, 5.8×107 on Tryptic soy agar and 5.8×107on Nutrient agar. In T2, the average weight gain was 16.22±16.09b grams and average length gain was 12.97±7.79b cm. The total viable count on Eosin methylene blue was 7×107, 5.5×107 on Tryptic soy agar and 5.8×107on Nutrient agar. In T3, the average weight gain was 37.88±27.43c grams, while the average length gain was recorded as 16.48±12.56c cm. However, the total viable count for treatment 3 was 6.4×10 on Eosin methylene blue, 4.8×107 on Tryptic soy agar and 5.2×107on Nutrient agar. In T4, the average weight gain was 44.22±31.67d grams, while the average length gain was 15.25±10.49d cm. The total viable count was 4.3×107on Eosin methylene blue, 3.1×107 on Tryptic soy agar and 3.8×107 on Nutrient agar. The effect of Moringa oleifera on the growth of Oreochromis niloticus was found to be significant and 12% Moringa extract showed maximum length and weight gain and minimum feed conversion ratio with the least microbial count in fish intestine.

Research on low-cost bio-adsorbents for the removal of harmful substances from effluents has recently attracted significant attention. In this study, three types of amino-silane-modified lignins (ASLs) with primary, secondary, and tertiary amine groups were prepared, and their adsorption behavior toward cationic and anionic dyes was investigated. Chemical structural analyses indicated that the three amino-silane reagents resulted in different molecular self-assembly structures on the lignin surface. The ASLs exhibited enhanced thermal stabilities and increased surface areas with different surface charges in different pH ranges. Owing to the high density of primary, secondary, and tertiary amine groups, the ASLs exhibited excellent adsorption capacities for cationic and anionic dyes. Additionally, they selectively adsorb anionic and cationic dyes according to the pH conditions. The ASL with primary amine had the highest adsorption capacity for Methylene blue and Congo red, reaching 187.27 and 293.26 mg·g -1 , respectively, followed by ASLs with the secondary amine and tertiary amine. All adsorption processes followed the Langmuir and Temkin isotherms and had pseudo-second-order kinetics. The hypothesized adsorption mechanism mainly involves electrostatic interaction, NH-π interaction, hydrogen bonding interaction and π-π interaction., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

This study aims to prepare activated carbon from an interesting biomaterial, corresponding to the cores of Ziziphus lotus , for the first time to the best of our knowledge, according to a manufacturing process based on its chemical and thermal activation. These cores were chemically activated by sulfuric acid for 24 h and then carbonized at 500°C for 2 hours. The obtained activated carbon was characterized by scanning electron microscopy, X-ray diffraction, Fourier transform infrared spectroscopy, and Brunauer-Emmett-Teller (BET) analysis. The adsorption of methylene blue (MB) on the activated carbon was evaluated, by Langmuir and Freundlich models examination, in order to explain the adsorption efficiency in a systematic and scientific way. Moreover, pseudo-first-order and pseudo-second-order kinetic models were used to identify the mechanisms of this adsorption process. The characterization results showed an important porosity (pore sizes ranging from 10 to 45  µ m), a surface structure having acid groups and carboxylic functions, and a specific surface of 749.6 m 2 /g. Results of the MB adsorption showed that this process is very fast as more than 80% of MB is adsorbed during the first 20 minutes. In addition, increasing the contact time and temperature improves the MB removal process efficiency. Moreover, this adsorption's kinetic modeling follows the pseudo-second-order model. Furthermore, data on the adsorption isotherm showed a maximum adsorption capacity of 14.493 mg/g and fit better with the Langmuir model. The thermodynamic parameters (∆G 0 , ∆S 0 , and ∆H 0 ) indicate that the adsorption process is endothermic and spontaneous. Therefore, Ziziphus lotus can be used as a low-cost available material to prepare a high-quality activated carbon having a promising potential in the wastewater treatment., Competing Interests: The authors declare that there are no conflicts of interest., (Copyright © 2022 Ibrahim Touzani et al.)

An innovative approach to characterize the reactivity of metallic iron (Fe 0 ) for aqueous contaminant removal has been in use for a decade: The methylene blue method (MB method). The approach considers the differential adsorptive affinity of methylene blue (MB) for sand and iron oxides. The MB method characterizes MB discoloration by sand as it is progressively coated by in-situ generated iron corrosion products (FeCPs) to deduce the extent of iron corrosion. The MB method is a semi-quantitative tool that has successfully clarified some contradicting reports on the Fe 0 /H 2 O system. Moreover, it has the potential to serve as a powerful tool for routine tests in the Fe 0 remediation industry, including quality assurance and quality control (QA/QC). However, MB is widely used as a 'molecular probe' to characterize the Fe 0 /H 2 O system, for instance for wastewater treatment. Thus, there is scope to avoid confusion created by the multiple uses of MB in Fe 0 /H 2 O systems. The present communication aims at filling this gap by presenting the science of the MB method, and its application and limitations. It is concluded that the MB method is very suitable for Fe 0 material screening and optimization of operational designs. However, the MB method only provides semi-quantitative information, but gives no data on the solid-phase characterization of solid Fe 0 and its reaction products. In other words, further comprehensive investigations with microscopic and spectroscopic surface and solid-state analyses are needed to complement results from the MB method., (Copyright © 2021. Published by Elsevier Ltd.)

Locally generated food wastes, such as Arabic coffee ground (ACG) and olive oil cake (OOC) were converted to N-ACG: OOC - 3 hydrochar (HC) through simultaneous co-hydrothermal carbonization (Co-HTC) and chemical activation. The optimized ACG: OOC mass ratio (g: g) and chemical activation agent used were 1.2: 0.8 and 0.1 M HNO 3 , respectively. Spectroscopic analyses confirmed the dominance of oxygen-containing functionalities, whereas the X-ray diffraction pattern displayed peaks for both sucrose and cellulose on N-ACG: OOC - 3. The developed HC was tested for methylene blue (MB) and crystal violet (CV) adsorption in aqueous systems. Batch scale adsorption studies showed pH, initial concentration (C o ), time (t), and temperature (T) dependent dye uptake. Maximum dye uptake was observed at pH 7, with 50 - 70% and 76 - 90 % CV and MB removal achieved within 15 min at varied C o : 50 - 200 mg/L. Adsorption was governed by multiple mechanisms, including hydrogen bonding, electrostatic interactions, π-π interactions, and n-π interactions. Dye elution was higher in ethanol (EtOH: C 2 H 5 OH), and CV elution (50.8%) was more significant than MB elution (14.8%)., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

In this work, the transformation of soybean industrial bio-residue with limited practical applications, into a multifunctional carbonaceous adsorbent (SBAC) via one-step microwave-irradiation has been succeeded. The surface porosity, chemical compositions, functionalities and surface chemistry were featured by microscopic pore-textural analysis, elemental constitution analysis, morphological characterization and Fourier transform infra-red spectroscopy. The adsorptive performance of SBAC was evaluated in a batch experiment by adopting different classes of water pollutants, specifically methylene blue (MB), acetaminophen and 2,4-dichlorophenoxyacetic acid (2,4-D). The equilibrium uptakes were analyzed with respect to the non-linearized Langmuir, Freundlich and Temkin isotherm equations. The unique features of SBAC, specifically the antimicrobial and antifungal efficacies were examined against gram-positive/negative bacteria and fungi species. An ordered microporous-mesoporous structure of SBAC, with the BET surface area and total pore volume of 1696 m 2 /g and 0.94 m 3 /g, respectively, has been achieved. The equilibrium data of MB and acetaminophen were found to be in good agreement with the Langmuir isotherm model, with the monolayer adsorption capacities (Q o ) of 434.57 mg/g and 393.31 mg/g, respectively. The adsorptive experiment of 2,4-D was best fitted to the Freundlich isotherm equation, with the Q o of 253.17 mg/g. The regeneration performance of the spent SBAC under microwave-irradiation could maintain at 69.42-79.31%, even after five (5) adsorption-regeneration cycles. SBAC exhibited excellent inhibition efficiencies against gram-positive/negative bacteria and fungi species, with the inhibition zones at 14.0-28.0 mm. This newly developed SBAC appears to be a new powerful candidate for the remediation of different classes of water contaminants, and novel antibacterial and antifungal agents against biological contaminations. The novel concept of "turn waste into wealth" in a cost-effective and energy saving manner for environmental preservation has been successfully accomplished., (Copyright © 2021 Elsevier Inc. All rights reserved.)

The efficiency of the living biomass of the microalga Chlamydomonas moewusii in removing methylene blue dye is determined. The kinetics, equilibrium isotherms, and the effects on this process of the pH, contact time, and initial concentration of the dye are studied. Fourier transform infrared spectrometry and point of zero charge are used to characterize the biomass and explore the process. The maximum removal capacity derived from the Langmuir isotherm is 212.41 ± 4.55 mg/g after 7 h of contact time at pH 7. The removal process is rapid because kinetic studies revealed that the best fit of the data is with pseudo-third-order kinetics. The removal efficiency is dependent on the pH; as the pH increased, the efficiency is higher. These results show that the living biomass of this microalga is a very efficient biosorbent and therefore very suitable for the removal of methylene blue from aqueous solutions.

Hydrochar (AAHC) with rich carboxylate groups was prepared by one-step hydrothermal carbonization (HTC) of bamboo and acrylic acid with the presence of ammonium persulphate, and then activated by a sodium hydroxide solution. AAHC was featured by elemental analysis, SEM, XPS, FTIR, Zeta potential analysis and N 2 adsorption-desorption isotherms, and applied to test adsorptive ability of methylene blue (MB) by batch sorption experiments. Despite a small Brunauer-Emmett-Teller (BET) surface area of 5.03 m 2 ·g -1 , AAHC has excellent MB adsorbing capacity owing to the richness of carboxylate groups. Compared with hydrochar produced without adding ammonium persulphate, AAHC exhibits larger BET surface, pore volume and carboxylate groups, indicating a small amount of ammonium persulfate plays an important role in HTC in addition to the free radical initiator. This work provides a facile and cheap method combining HTC and polymerization for preparation of carboxylate-rich hydrochar., (Copyright © 2021 Elsevier B.V. All rights reserved.)

The potential ability of synthesized PPy-Fe 3 O 4 -SW nano-composite to remove Methylene Blue (MB) from synthetic textile dye solution was investigated under batch conditions. Through parametric studies, the influence of process parameters namely solution pH, on the effective performance of nano-composite was studied. PPy - Fe 3 O 4 - SW nano-composite removed 99.14% of MB at the optimized conditions of pH-10, temperature - 25 °C, initial MB concentration - 50 mg/L, nano-composite dosage - 20 mg and contact time - 20 min. PPy - Fe 3 O 4 - SW nano-composite has a maximum sorption capacity of 666.66 mg/g. The kinetics and isotherm study revealed that the chromium adsorption obeys pseudo second order (PSO) model (R 2  = 0.9941) and Freundlich isotherm (R 2  = 0.9910) respectively. The PSO kinetic constant (K 2 ) was found to be 0.000442 (g/mg) min. The thermodynamic feasibility was confirmed through negative values of standard free energy at all tested conditions. The characteristics of adsorption study were analyzed and the results of FTIR, SEM and EDS confirmed the uptake of MB by PPy-Fe 3 O 4 -SW nano-composite., (Copyright © 2021. Published by Elsevier Ltd.)

Adsorbents reported for liquid phase decontamination under both aqueous and non-aqueous media are all dispersed phase sorbents that further require a tedious separation step post adsorption. Herein, a monolith, highly porous, and mechanically robust scaffold was synthesized for the adsorption of pollutants from both aqueous and non-aqueous media with facile separation and regeneration. Methylcellulose-tannic acid complex particles were prepared and systematically decorated on the surface of interpenetrating polymer network (IPN) scaffold via Pickering emulsion. Due to the surface coating of the particles, plausible amphiphilic adsorption of quinoline (QUI) and methylene blue (MB) was achieved from fuel and water, respectively. The hydroxyl (OH-) and carboxyl (COOH-) groups of tannic acid, alginate, and polyacrylic acid created hydrogen bonding, electrostatic interaction, acid-base interaction, and π-π stacking. Maximum adsorption capacity of 791.17 mg/g MB and 460.92 mg/g QUI was recorded with facile separation, excellent adsorbent regeneration, and reusability. Although both followed the pseudo-second-order adsorption kinetic model, a different mechanism was identified to govern the adsorption under aqueous and non-aqueous environment i.e. only the surface particles were active for QUI adsorption while the scaffold was also involved for MB adsorption., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Herein, mesoporous activated carbon (AC) was prepared through potassium hydroxide (KOH) activation of hydrochar derived from the hydrothermal carbonization (HTC) of chickpea stem (CS), and successfully applied to remove methylene blue (MB) dye from aqueous solutions in a batch system. The HTC-CSAC was prepared depending on different impregnation ratios (hydrochar:KOH, 50-150%), impregnation times (12-48 h), activation temperatures (400-600 ° C ) and activation times (30-60 min). To define HTC-CSAC, various analytical techniques such as iodine adsorption number (IAN), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and Brunauer-Emmett-Teller (BET) were used. In the removal process of MB by the best HTC-CSAC with a high IAN of 887 mg g -1 obtained under conditions including impregnation ratio of 70%, activation time of 45 min, activation temperature of 600 ° C and impregnation time of 24 h, the effects of adsorption parameters such as pH factor (2-10), adsorbent dosage (50-100 mg), initial MB concentration (40-80 mg/L) and contact time (90-180 min) were studied. Besides, a detailed evaluation of the adsorption mechanism for the removal of MB by HTC-CSAC was performed. The Langmuir model indicated the best isotherm data correlation, with a maximum monolayer adsorption capacity ( Q max ) of 96.15 mg g -1 . The adsorption isotherm findings demonstrated that the MB removal process is feasible, and that this process takes place through the physical interaction mechanism. Additionally, the HTC-CSAC adsorbent exhibited a high regeneration and reuse performance in MB removal. After five consecutive adsorption-desorption cycles, HTC-CSAC maintained the reuse efficiency of 77.86%. As a result, the prepared HTC-CSAC with a high BET surface area of 455 m 2 g -1 and an average pore diameter of 105 Å could be recommended as a promising and reusable adsorbent in the treatment of synthetic dyes in wastewaters.

A novel one-pot synthesis method was developed to prepare modified hydrochar by co-hydrothermal carbonization of waste distillers grains using low-cost clay minerals (attapulgite or vermiculite). The loading of the clay minerals onto hydrochar surfaces altered the structure and surface composition of the hydrochar such that the clay-modified hydrochars showed better ability to adsorb methylene blue and phosphate in aqueous solution than the pristine hydrochar. The maximum methylene blue and phosphate adsorption capacities of the modified hydrochar reached 340.3 and 96.9 mg g -1 , respectively, comparable or higher than that of many commercial sorbents. Multiple mechanisms, including electrostatic attraction, ion exchange, complexation, and physical adsorption, controlled the adsorption process. These results highlight excellent potential for distillers grains-derived hydrochar-clay composites as an environmental sorbent, capable of removing a variety of contaminants from aqueous solutions., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

In this work, sugarcane bagasse waste (SBW) was used as a lignocellulosic precursor to develop a high-surface-area activated carbon (AC) by thermal treatment of the SBW impregnated with KOH. This SBW activated carbon (SBWAC) was characterized by crystallinity, porosity, surface morphology and functional groups availability. The SBWAC exhibited Type I isotherm which corresponds to microporosity with high specific surface area of 709.3 m 2 /g and 6.6 nm of mean pore diameter. Further application of SBWAC as an adsorbent for methylene blue (MB) dye removal demonstrated that the adsorption process closely followed the pseudo-second order kinetic and Freundlich isotherm models. Conversely, a thermodynamic study revealed the endothermic nature and spontaneity of MB dye adsorption on SBWAC with high acquired adsorption capacity (136.5 mg/g). The MB dye adsorption onto SBWAC possibly involved electrostatic interaction, H-bonding and π-π interaction. This work demonstrates SBW as a potential lignocellulosic precursor to produce high-surface-area AC that can potentially remove more cationic dyes from the aqueous environment.

Historically, lignin has been produced as a waste by-product in industrial processes. In this study, lignosulfonate nanoparticles were fabricated and freeze-dried for use as a precursor material for carbonization. The use of the carbonized lignins for the adsorption of textile effluent as a value-added application is demonstrated. Characterization of the as received lignin (LN) and the developed nano-based freeze-dried lignin (NFLN) were performed prior to and after carbonization at 600, 750, 900 and 1050 °C. Using probe sonication, lignosulfonates were broken down into nanoparticles with lower weight-average molecular weight as verified by dynamic and static light scattering techniques. The difference between the LN and the NFLN was determined to be primarily morphological as the sonication and freeze-drying process imparted a platelet-like shape to the NFLN biocarbons and an increased surface area, while the remaining functionality was similar. The adsorption behaviour of methylene blue (MB), a synthetic cationic dye, was investigated using adsorption isotherm and kinetic models, with the NFLN exhibiting a maximum adsorption capacity of 109.77 mg/g. Overall, electrostatic attraction and hydrogen bonding contribute significantly to the MB adsorption. Further preliminary work was also performed demonstrating the coating of polyurethane foam for the adsorption of MB. These renewable biocarbons show promising properties for use as additive in adsorbent, coating, pigment or as a filler in polymer composite applications., (Copyright © 2021 Elsevier B.V. All rights reserved.)

A sensitive and reliable method was developed to determine methylene blue (MB) and its metabolite residues, including azure A (AZA), azure B (AZB), and azure C (AZC) in aquatic products by HPLC-MS/MS. The samples were extracted by acetonitrile and cleaned up by alumina-neutral (ALN) cartridges. The analytes were separated on a Sunfire C18 column (150 mm × 2.1 mm, 5 µm). The method was validated according to the European criteria of Commission Decision 2002/657/CE. Good linearity between 1-500 µg/L was obtained with correlation coefficients ( R 2 ) greater than 0.99. The limit of quantification (LOQ) was 1.0 µg/kg. The average recoveries at three levels of each compound (1, 5, and 10 µg/kg) were demonstrated to be in the range of 71.8-97.5%, with relative standard deviations (RSDs) from 1.05% to 8.63%. This method was suitable for the detection of methylene blue and its metabolite residues in aquatic products.

The aim of this study was to develop an HPLC method for simultaneous quantification of metformin (MET) and methylene blue (MB) in in vitro skin permeation/retention studies, in which retention was evaluated in the different layers of the skin [stratum corneum (SC) and the viable epidermis + dermis (VE + D)]. The method was validated considering the following parameters: specificity, linearity, quantitation limit (LOQ), recovery, precision and accuracy. Calibration curves were obtained using the following six matrices: methanol, water, methanolic extracts from the SC and VE + D spiked with the drugs and drugs extracted from the SC and VE + D. The precision, accuracy and LOQ of the method were evaluated in water and in VE + D and SC, applying the drug extraction process. The results show that the method is selective and linear for both drugs. The precision and accuracy values, independent of matrix and drug, were below the limit of 15%. The LOQ of MB was defined as 0.4 μg/ml in the VE + D and SC and 0.8 μg/ml in water. The LOQ of MET was defined as 0.8 μg/ml in the VE + D and SC and 0.4 μg/ml in the water. The recovery of the method was adequate, consistent and reproducible for the concentration range of 0.4-10 μg/ml for MB (73.3-92.1%) and 0.8-10.0 μg/mL for MET (72.4-94.4%). This method has a potential application in the development of formulation for skin delivery of MB and MET., (© 2021 John Wiley & Sons, Ltd.)

In this study, natural core-shell structure activated carbon beads (ACBs) from Litsea glutinosa seeds were successfully produced, characterized, and applied for adsorption of methylene blue (MB). The ACBs were prepared using single-step carbonization-activation with NaHCO 3 at the optimized activation temperature, time, and activating agent concentration of 450 °C, 60 min, and 5%, respectively. Batch experiments were performed to determine the optimum adsorption conditions, suitable kinetic and isotherm models, and thermodynamic parameters for the adsorption of MB onto ACBs. The results showed that the ACBs were displayed as highly porous natural core-shell spheres with a diameter of about 5 mm. The adsorption of MB dye on ACBs was a spontaneous endothermic process, followed the Langmuir isotherm and the pseudo-second-order kinetic models with the rate-controlling step of both external diffusion and intra-particle diffusion. At the optimum conditions (pH of 9, the contact time of 10 h, the temperature of 40 °C, and an adsorbent dosage of 6 g/L), the maximum adsorption capacity reached 29.03 mg/g. The thermal method turned out to be more suitable for regenerating ACBs compared to the chemical method. The ACBs exhibited high reusability and stability, its adsorption efficiency could maintain more than 90% after five consecutive cycles of use. The electrostatic attraction, π-π interaction, hydrogen bonding, and pore-filling were identified as primary contributions to the adsorption mechanism. The overall results revealed that the ACBs could be used as a potential adsorbent for removing MB from water media., (Copyright © 2020 Elsevier Inc. All rights reserved.)

Methylene blue (MB) is the cationic dye that is widely used for coloring cotton, wool, and silk. Since MB is harmful to human beings and toxic to microorganisms, there is the need to find cheap and efficient methods for removal of MB from wastewater prior to disposal into natural waters. In the present study, MB adsorption potential of MgO/AC prepared using a sol-gel-thermal deep-coating method was compared with the activated carbon (AC). The central composite design (CCD) as a method of the response surface methodology (RSM) was applied to minimize the number of runs and process optimization. The characterization of the microporous MgO/AC composite showed that the magnesium oxide nanoparticles were successfully coated on the AC and the BET specific surface area of AC and MgO/AC were 1,540 and 1,246 m 2 /g, respectively. The MB removal efficiency and the maximum adsorption capacity of AC and MgO/AC were 89.6, 97.5% and 571.7, 642.3 mg/g, respectively under optimum operational conditions of initial dye concentration of 100.9 mg/L, the adsorbent dosage of 69.4 mg/100 mL, pH of 10.2 and contact time of 149.1 min. According to an analysis of variance (ANOVA), the initial dye concentration and its interaction with the other effective factors have a large impact on adsorption efficiency. Furthermore, the mechanism of adsorption followed the Langmuir isotherm (R 2 = 0.9935, Δq e = 2.9%) and adsorption kinetics fitted by the pseudo-second-order model (R 2 = 0.9967, Δq e = 6.6%). Finally, our results suggest that the prepared MgO/AC is an efficient and promising material for dye wastewater treatment.

Pods of the forest species Caesalpinia echinata were used as an alternative adsorbent to remove bright blue (BB) and methylene blue (MB) dyes. The raw and acid-treated samples were characterized by techniques like SEM, XRD, and FTIR. The acid-treated pod sample was characterized by an amorphous structure containing several cavities, bumps, and functional groups. The Elovich model was the most satisfactory to describe the adsorption kinetic data. The isothermal studies were better described by the Langmuir model for BB dye, with a maximum capacity of 261 mg g -1 , and Tóth model for MB dye, giving a maximum capacity of 288 mg g -1 . The thermodynamic study indicated a spontaneous and favorable process and endothermic nature for both dyes. In the treatment of two simulated effluents containing a mixture of different compounds such as dyes and salts, to simulate real wastewaters, the adsorbent was highly efficient, presenting around 80% of color removal for both effluents. Therefore, the acid-treated pods of Caesalpinia echinata have great potential to be applied as an alternative adsorbents in treating colored effluents in discontinuous systems.

In this work, a simple and feasible approach for converting waste vinasse generated from the alcohol industries into high value-added activated carbon (AC) was proposed. The obtained AC possessed abundant micropores with micropore volume of 0.9613 cm 3 /g and ultrahigh specific surface areas (2015 m 2 /g), indicating prominent adsorption capacity. The adsorption ability of AC to cationic methylene blue (MB) was investigated systematically. The resultant AC exhibited superior adsorption ability to MB with a maximum amount of 2251 mg/g, derived from its excellent pore textural features and abundant surface O-containing functional groups. Moreover, AC showed excellent removal efficiency for treating industrial polyacrylonitrile wastewater with 99% removal within 60 min. Our results provide great inspirations in solid waste treatment and their high value-added transformation, meanwhile exploit a promising application of AC for practical wastewater purification., (Copyright © 2020. Published by Elsevier Ltd.)

The utilization of nanoparticle-polymer bead hybrid nanostructures as a SERS substrate depends on the control of the deposition, density, and distribution of nanoparticles on the bead surface. Here we demonstrate the fabrication of a large area SERS substate via a two- step DNA mediated assembly of gold nanoprisms and polystyrene (PS) beads into a large ensemble of beads that are densely coated with nanoprisms. First, nanoprisms are loaded on PS beads through DNA hybridization. The close packed arrangement of anisotropic nanoprisms in different orientations on a bead surface results in a plasmonic substrate with a variable nanogap size ranging 1-20 nm. Nanoprisms-coated beads are then assembled into a large stack or aggregate of beads using a DNA-induced crystallization approach. Each aggregate consists of 20-50 nanoprisms-coated beads, leading to the formation a large area of three-dimensional SERS substrate with a high-density of hot spots for SERS enhancement. An excellent enhancement factor (EF) of [Formula: see text] and a very high detection sensitivity (up to 10 -10 M) are observed for the analysis of a probe molecule (Methylene blue) using the SERS substrate.

Two novel ecological and low-cost adsorbents were prepared from seed residues of the tree species Anadenanthera macrocarpa and Cedrela fissilis for the removal of methylene blue dye in water. The materials were comminuted and characterized by different techniques. The particles of samples have a rough surface with cavities. The optimum dosage and pH for both materials were 1 g L -1 and pH 8. The pseudo-second-order model was the most suitable for describing the adsorption kinetics for both systems. The Anadenanthera macrocarpa presented a maximum experimental capacity of 228 mg g -1 , while the Cedrela fissilis, a similar capacity of 230 mg g -1 at 328 K. The Tóth model was proper for describing the equilibrium curves for both systems. The thermodynamic indicators show that the adsorption process is spontaneous and endothermic for both materials. The application of materials for the simulated effluent treatment showed 74 and 78% of color removal using Anadenanthera macrocarpa and Cedrela fissilis samples, respectively. Overall, seed residues of Anadenanthera macrocarpa and Cedrela fissilis could be potentially applied for adsorptive removal of colored contaminants in wastewater.

The chemical compositions of macroalgae are protein; cholesterol, fatty acid, and lignin which mostly construct from hydroxyl and amine groups. The lignin as a key structure in the tissues of macroalgae was modified using the sulfation pathway. A novel environmental friendly adsorbent Cu-BTC@Algal was synthesized by incorporated Cu-BTC nanoparticles onto sulphated-Macroalgae biomass under solvothermal conditions and characterized by XRD, FTIR, and N 2 adsorption-desorption isotherms. The removal rate of Cu-BTC@Algal was quite greater than that of Cu-BTC, showing that the adsorption performance of porous Cu-BTC can be improved through the modification of algal. Further study revealed that Cu-BTC@Algal exhibited a fast adsorption rate and selective adsorption ability towards the cationic dyes in aqueous solution. The removal rate was up to 97% for cationic dyes methylene blue (MB) and 68% for methyl orange (MO) at intervals 10 min. The influences including initial concentration, and contact time of MB/MO adsorption onto modified algal biomass, Cu-BTC and Cu-BTC@Algal were investigated in detail. The kinetic study indicated that the adsorption of MB/MO onto Cu-BTC@Algal followed the pseudo second-order model. The isotherm obtained from experimental data fitted the Langmuir model, yielding maximum adsorption capacity of 42, 73 and 162 mg g -1 for algal, Cu-BTC and Cu-BTC@Algal, respectively., (Copyright © 2020 Elsevier B.V. All rights reserved.)

Flowers-like ZnO structures were synthesized using Arabic Gum (AGZnO) or Karaya Gum (KGZnO). The AGZnO and KGZnO were characterized by X-ray diffractometry, Fourier Transformed Infrared, Scanning Electron Microscopy, Photoluminescence, nitrogen adsorption/desorption and diffuse reflectance techniques. The materials were tested in the discoloration of Methylene Blue (MB) dye under visible light and scavenger studies were also performed. The toxicity of the MB irradiated was investigated in bioassays with Artemia salina. The structural characterization demonstrated the formation of hexagonal ZnO. All samples presented flower-like morphology with presence of mesopores identified by BET method. The optical properties indicated band gap of 2.99 (AGZnO) and 2.76 eV (KGZnO), and emission in violet, blue and green emissions also were observed. The KGZnO demonstrated better photocatalytic performance than the AGZnO, and scavenger studies indicated that OH radicals are the main species involved in the degradation of the pollutant model. The photodiscoloration of MB solution did not demonstrate toxicity. Therefore, KGZnO is a promising material for photocatalysis application., (Copyright © 2020 Elsevier B.V. All rights reserved.)

This study represents the first ever work on a novel oxone treated hydrochar as an adsorbent for the efficient removal of different contaminants from aqueous solutions. Pine wood hydrochar (HC) was prepared by hydrothermal treatment at 300 °C and oxidized with oxone to produce oxidized pine wood hydrochar (OHC). Different analytical tools such as elemental analysis, FTIR, TGA, FE-SEM, and BET were used for the characterization of the OHC. Conductometric titration of OHC showed a substantial increase from 22 μmol/g to 600 μmol/g in the hydrochar carboxylic content. The OHC sorption performance was assessed by using Pb(II) ions and methylene blue (MB) dye as two models of contaminants. Sorption benchmarks were performed by varying the contaminant initial concentration, time, and temperatures. Sorption kinetic data was fitted well to the pseudo-second order kinetic model with high correlation coefficients (R 2  > 0.99) and isothermal data was fitted to the Langmuir model. The highest adsorption capacities for MB and Pb(II) were 86.7 mg/g and 46.7 mg/g, respectively. This study proves that oxone treatment could be a potential sustainable oxidation method to tune the hydrochar surface to increase selectivity towards heavy metal ions and dye sorption., 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 © 2020 Elsevier Ltd. All rights reserved.)

Well-aligned ZnO nanorod arrays were assembled on activated carbon fibers by a stepwise sequence of sol-gel and hydrothermal synthesis methods. These ZnO nanorod arrays on activated carbon fibers having different characteristics such as surface area, rod concentration, aspect ratio and defect level, were applied as catalysts for the photodegradation of an aqueous methylene blue solution. They showed very promising methylene blue adsorbility in the dark (ca. 0.025-0.031 mg methylene blue m -2 catalyst, vs. 0.072 mg methylene blue m -2 activated carbon fibers). Significantly, the defect level of ZnO nanorod arrays has a major effect on the turnover frequency compared to other characteristics. A synergistic effect between activated carbon fibers and ZnO nanocrystals on enhancing turnover frequency was more significant for the well-assembled ZnO nanorod arrays on activated carbon fibers catalysts compared to the mechanically mixed ZnO powder with activated carbon fibers catalyst. Further, turnover frequency for the ZnO nanorod arrays on activated carbon fibers (0.00312 mol methylene blue mol ZnO -1 h -1 ) was twice higher than that for the corresponding bare ZnO nanorod arrays, and 3 times higher than that for a commercial ZnO powder. In addition, ZnO nanorod arrays on activated carbon fibers show high degradation (77.5%) and mineralization (55.0%) levels for methylene blue, and also good reusability (or stability) as demonstrated by a sequential 5-time recycle routine. These outstanding features indicate that activated carbon fibers supported ZnO nanorod arrays have significant potential to be used as catalysts for photodegradation., 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 © 2020 The Author(s). Published by Elsevier Ltd.. All rights reserved.)

Titanate nanotubes (TNTs) were hydrothermally synthesized from commercially available TiO 2 powder and were characterized by XRD, SEM/EDX, and TEM. The as-prepared TNTs were used to remove organic dye, Methylene Blue (MB) from aqueous media by batch mode at 25 ± 2 °C, at pH 6.8 ± 0.2. The MB removal process followed two mechanisms of adsorption (absence of UV light) and photodegradation on precursor's surfaces. Photo-illumination study revealed the ∼98% MB removal with the dose of 3 g/L TNT with an initial concentration of 10 mg/L. Adsorptive capacity of TNT was evaluated from the Langmuir isotherm and found to be 151.51 mg/g. Dimensionless equilibrium parameter R L value suggested the favourable but the free energy changes (ΔG°) value (10.752 kJ/mol) suggested the non-spontaneity of the adsorption process. Adsorption followed the pseudo-second order kinetics model best. MB adsorption onto TNT surfaces followed neither pore diffusion nor film diffusion. Studies conducted in the presence of different foreign ions as well as varying pH of the media to understand their effects in the process if any. Turnover studies were also conducted. A probable photodegradation mechanism was proposed. Finally, TNT was used to remove MB from spiked pond water collecting from the KISS University, including pre- and post analysis of water quality.