Synthesis of hydrochar from date palm seeds using microwave-enhanced hydrothermal carbonization and its application in dyes removal.

This work reports new findings on the preparation of hydrochar from date palm (Phoenix dactylifera) seeds through the application of the microwave hydrothermal carbonization (HTC) method. Optimization investigations involving temperatures and reaction times were conducted to establish the highest yield, achieving a maximum yield of 60.87%. The prepared material was then impregnated in phosphoric acid and carbonized in the tube furnace at 550 °C for 1.5 h with a nitrogen flow of 50 CCM. The samples were characterized via scanning electron microscopy (SEM), Brunauer-Emmet-Teller (BET) and Fourier transform infrared (FTIR). The samples showed remarkable BET surface areas following activation, reaching up to 992 m2·g-1. The substance was subsequently used to absorb methylene blue with good fitting to the Freundlich and Redlich-Peterson isotherm and achieved a peak adsorption capacity of 196.6 ± 3.9 mg·g-1.

This study involves the preparation of hydrochar through microwave-assisted hydrothermal carbonization (HTC) of date palm seeds. It explores the impact of different process parameters, such as power, reaction temperatures, and timing on the mass yield and BET surface area of the hydrochars. Additionally, the prepared material undergoes chemical activation with phosphoric acid, and its efficacy in extracting methylene blue (MB) from an aqueous solution is assessed. This research is particularly novel as it represents the first comprehensive investigation into the use of microwave-derived and phosphoric acid-activated hydrochar for MB extraction.

A facile two-step hydrothermal preparation of 2D/2D heterostructure of Bi2WO6/WS2 for the efficient photodegradation of methylene blue under sunlight.

A facile two-step hydrothermal method was successfully used to prepare a photocatalyst Bi2WO6/WS2 heterojunction for methyl blue (MB) photodegradation. Fabricated photocatalysts were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), energy-dispersive X-ray analysis (EDX), and X-ray photoelectron spectroscopy (XPS). Band gap measurements were carried out by diffuse reflectance spectroscopy (DRS). Results indicated that the prepared heterostructure photocatalyst has increased visible light absorption. Photocatalytic performance was evaluated under sunlight irradiation for methylene blue (MB) degradation as a model dye. Variations in pH (4-10), amount of catalyst (0.025-0.1 g/L), and initial MB concentrations (5-20 ppm) were carried out, whereas all prepared catalysts were used to conduct the tests with a visible spectrophotometer. Degradation activity improved with the pH increase; the optimum pH was approximately 8. Catalyst concentration is directly related to degradation efficiency and reached 93.56% with 0.075 g of the catalyst. Among tested catalysts, 0.01 Bi2WO6/WS2 has exhibited the highest activity and a degradation efficiency of 99.0% in 40 min (min) for MB. MB photodegradation follows pseudo-first-order kinetics, and obtained values of kapp were 0.0482 min-1, 0.0337 min-1, 0.0205 min-1, and 0.0087 min-1 for initial concentrations of 5 ppm, 10 ppm, 15 ppm, and 20 ppm, respectively. The catalyst was reused for six cycles with a negligible decrease in the degradation activity. Heterostructure 0.01 Bi2WO6/WS2 has exhibited a photocurrent density of 16 µA cm-2, significantly higher than 2.0 and 4.5 µA cm-2 for the pristine WS2 and Bi2WO6, respectively. The findings from these investigations may serve as a crucial stepping stone towards the remediation of polluted water facilitated by implementing such highly efficient photocatalysts.

Green synthesis of iron oxide nanoparticles derived from water and methanol extract of Centaurea solstitialis leaves and tested for antimicrobial activity and dye decolorization capability.

In this research, nanoparticles derived from water extract of Centaurea solstitialis leaves were used as green adsorbent in Fenton reaction for Reactive Red 180 (RR180) and Basic Red 18 (BR18) dyes removal. At optimum operating conditions, nanoparticles proved high performance in the tested dyes removal with more than 98% of removal elimination. The free-radical scavenging, DNA nuclease, biofilm inhibition capability, antimicrobial activity, microbial cell viability, and antimicrobial photodynamic therapy activities of the iron oxide nanoparticles (FeO-NPs) derived from water and methanol extract of plant were investigated. Each of the following analysis: SEM-EDX, XRD, and Zeta potential was implemented for the prepared NPs characterization and to describe their morphology, composition and its behavior in an aqueous solution, respectively. It was found that, the DPPH scavenging activities increased when the amount of nanoparticles increased. The highest radical scavenging activity achieved with FeO-NPs derived from water extract of plant as 97.41% at 200 mg/L. The new green synthesized FeO-NPs demonstrated good DNA cleavage activity. FeO-NPs showed good in vitro antimicrobial activities against human pathogens. The results showed that both synthesized FeO-NPs displayed 100% antimicrobial photodynamic therapy activity after LED irradiation. The water extract of FeO-NPs and methanol extract of FeO-NPs also showed a significant biofilm inhibition.

Thermo-Chemical Modification of Cellulose for the Adsorptive Removal of Titan Yellow from Wastewater.

This research work focuses on the isolation and thermo-chemical modification of cellulose and its application as an adsorbent for the removal of organic pollutants. The used cellulose was collected from a locally available plant (Olive Europa) commonly called Zaitoon. The stem branches of Zaitoon were collected and then kept in water for 40-45 days at room temperature to extract the cellulose fibers. These cellulose fibers were then kept in the Soxhlet apparatus for washing in n-hexane for 72 h. The purified cellulose was divided into three parts: one part was subjected to thermal activation (TAC), the second was modified chemically (CMC) with Benzyl Chloride, while the last one remained un-functionalized (UFC). All the three forms of cellulose were characterized via FTIR and SEM, then utilized for the removal of Titan Yellow (TY) dye from aqueous media via adsorption process by varying the contact time, temperature, concentration of dye and type, and dose of adsorbent. The adsorption efficiencies of all adsorbents were compared under different experimental variables. Thermally activated cellulose showed the best results for the removal of TY compared with other materials. The calculated removal percentage of TY was found to be 97.69, 94.83, 94.83, and 98% under equilibrium conditions of contact time, temperature, adsorbent dose, and TY concentration. Similarly, the uptake capacities of TAC under optimal experimental conditions were found to be 19.56, 18.96, 18.52, and 18.75 mg/g. Thermodynamic studies of TAC, CMC, and UFC showed that the values of ΔG are negative, while those of ΔH and ΔS are positive in all cases and at all temperatures. This indicates that the TY elimination process is endothermic and spontaneous with an entropy-driven nature. The obtained results indicate that the as-fabricated low-cost biomaterials can effectively remove dyes from wastewater through physicochemical interactions. The removal process was influenced by the nature of the adsorbent and the operating variables.

Rapid, Highly-Efficient and Selective Removal of Anionic and Cationic Dyes from Wastewater Using Hollow Polyelectrolyte Microcapsules.

Herein, poly (allylamine hydrochloride) (PAH)/ poly (styrene sulfonic acid) sodium salt (PSS) microcapsules of (PAH/PSS)2PAH (P2P MCs) and (PAH/PSS)2 (P2 MCs) were obtained by a layer-by-layer method. The P2 MCs show high adsorption capacity for Rhodamine B (642.26 mg/g) and methylene blue (909.25 mg/g), with an extremely low equilibrium adsorption time (~20 min). The P2P MCs exhibited high adsorption capacities of reactive orange K-G (ROKG) and direct yellow 5G (DY5G) which were 404.79 and 451.56 mg/g. Adsorption processes of all dyes onto microcapsules were best described by the Langmuir isotherm model and a pseudo-second-order kinetic model. In addition, the P2P MCs loaded with reactive dyes (P2P-ROKG), could further adsorb rhodamine B (RhB) dye, and P2 MCs that had adsorbed cationic MB dyes could also be used for secondary adsorption treatment of direct dye waste-water, respectively. The present work confirmed that P2P and P2 MCs were expected to become an excellent adsorbent in the water treatment industry.

Superior removal of dyes by mesoporous MgO/g-C3N4 fabricated through ultrasound method: Adsorption mechanism and process modeling.

The present research concerns the synthesis of a mesoporous composite characterized with high surface area and superior adsorption capacity in order to investigate its efficacity in removing hazardous and harmful dyes molecules from water. The synthesized mesoporous composite, MgO/g-C3N4 (MGCN), was successfully prepared through the sonication method in a methanolic solution followed by an evaporation and a calcination process. The configuration, crystalline phase, surface properties, chemical bonding, and morphological study of the fabricated nanomaterials were investigated via XRD, BET, FESEM, HRTEM, XPS, and FTIR instrumentation. The obtained nanomaterials were used as sorbents of Congo Red (CR) and Basic Fuchsin (BF) dyes from aqueous solutions. Batch elimination experimental studies reveal that the elimination of CR and BF dyes from an aqueous solution onto the MGCN surface was pH-dependent. The highest removal of CR and BF pollutants occurs, respectively, at pH 5 and 7. The absorptive elimination of CR and BF dyes into the MGCN surface was well-fitted with a pseudo-second-order kinetics and Langmuir model. In this concern, the maximum nanocomposite elimination capacity for CR and BF was observed to be 1250 and 1791 mg g-1, respectively. This investigation confirms that MGCN composite is an obvious and efficient adsorbent of CR, BF, and other organic dyes from wastewater.

Recent advances in the removal of dyes from wastewater using low-cost adsorbents.

The presence of hazardous dyes in wastewater cause disastrous effects on living organisms and the environment. The conventional technologies for the remediation of dyes from water have several bottlenecks such as high cost and complex operation. This review aims to present a comprehensive outlook of various bio-sorbents that are identified and successfully employed for the removal of dyes from aqueous environments. The effect of physicochemical characteristics of adsorbents such as surface functional groups, pore size distribution and surface areas are critically evaluated. The adsorption potential at different experimental conditions of diverse bio-sorbents has been also explored and the influence of certain key parameters like solution pH, temperature, concentration of dyes, dosage of bio-sorbent and agitation speed is carefully evaluated. The mechanism of dyes adsorption, regeneration potential of the employed bio-sorbents and their comparison with other commercial adsorbents are discussed. The cost comparison of different adsorbents and key technological challenges are highlighted followed by the recommendations for future research.

Synthesis and Characterization of Hydroxyethyl Cellulose Grafted with Copolymer of Polyaniline and Polypyrrole Biocomposite for Adsorption of Dyes.

The emerging concepts of sustainable textiles and controlled production strategy demands ideally zero emissions of contaminants into the aquatic environment. However, the currently in-practiced conventional processes in textiles dispose of a number of contaminants especially super toxic synthetic dyes as effluents. In recent years, nanomaterials have become attractive choice for eco-friendly removal of organic dyestuff. Accordingly, this article reports synthesis and characterization of biocomposite wherein copolymer of polyaniline (PANI) and Polypyrrole (PPY) was grafted onto hydroxyethyl cellulose (HEC). Further, adsorption properties of as-prepared composite were evaluated using textile dyes Rhodamine B (RhB) and methyl Orange (MO)- as model adsorbate. The characterization of novel biocomposite (HEC/PANI-PPy) was carried out using Fourier Transform Infrared (FT-IR), Brunauer-Emmett-Teller analyzer (BET), Scanning Electron Microscope (SEM), and powder X-ray diffraction (XRD). The operational parameters such as dye initial concentration, adsorbent amount, pH and contact time were also studied to evaluate the efficiency level of the prepared biocomposite. Interestingly, the composite-mediated adsorption of RhB and MO followed pseudo-second order and the Langmuir isotherm. It is found that the adsorption capacity HEC/PANI-PPy is 30.06 and 29.3 for RhB and MO respectively. Thus, HEC/PANI-PPy is an inexpensive and highly efficient adsorbent that could be employed for could be employed for the separation and removal of toxic organic dyes from polluted textile effluents.

The preparation of thin-walled multi-cavities ß-cyclodextrin polymer and its static and dynamic properties for dyes removal.

Thin-walled multi-cavities ß-cyclodextrin polymers (Hß-CDs) were prepared by the suspension polymerization method using SiO2 nanoparticles as a template. The components and morphology structure of Hß-CDs were characterized by FTIR, BET, SEM, and TEM. The adsorption performances of the prepared nano-adsorbent Hß-CDs on crystal violet (CV), heavy metal ions, some cationic, neutral, and anionic dyes were investigated. The influences of the pH and ionic strength on CV adsorption by the Hß-CDs were explored. The correlation coefficient (R2) of pseudo-second-order kinetic model reached 0.9984 and the adsorption isotherm was closer to the Langmuir model. As the temperature increased, the R2 of the Freundlich isotherm model rose. Compared to anionic ones and heavy metal ions, Hß-CDs had a better adsorption efficiency for cationic dyes. Dynamic adsorption also indicated the thin-walled multi-cavities structure was beneficial for improving absorptivity and application of ß-cyclodextrin polymers. In addition, the Hß-CDs exhibited potentially applicable for the regeneration and reuse with the removal efficiency of CV was as high as 89% in the fourth cycle.

Study of simultaneous bioremediation of mixed reactive dyes and Cr(VI) containing wastewater through designed experiments.

Xenobiotic azo dyes and chromate (Cr(VI)) containing industrial wastewaters cause severe ecological problems. The present bioremediation study aims to treat wastewater containing Cr(VI) ions and mixed azo dyes (reactive red 21 (RR21) and reactive orange 16 (RO16)) by Pseudomonas aeruginosa 23N1. The process optimization of bioremediation is investigated using statistical designed experimental tool of response surface methodology. The ANOVA analysis is performed to evaluate optimal biodecolourization condition. This study shows that the amount of yeast extract has major influence on biodecolourization performance. The decolourization of individual RO16 and RR21 dye in presence of 60 mg/L of Cr(VI) ions is obtained as 88.5 ± 0.8 and 92.3 ± 0.7% for 100 and 150 mg/L initial dye concentrations, respectively. In this study, bacteria exhibit high Cr(VI) removal potential of ~ 99.1% against initial Cr(VI) concentration of 150 mg/L. The negative influence of Cr(VI) ions on biodecolourization is only noticed when initial Cr(VI) concentration in wastewater is found above 150 mg/L. The results reveal that bacteria studied here could be used to biodecolourize dyes even in high saline condition (> 6000 mg/L). The reduction of ~ 80% in American Dye Manufacturers Institute colour index value is achieved for mixed dyes solution containing 50 mg/L of both RR21 and RO16 dyes along with 50 mg/L Cr(VI) ions. Significant changes in the UV-visible and ATR-FTIR spectra are observed in treated water that confirms the biodegradation of dyes. Toxicity study with Vigna radiata reveals the non-toxicity of degraded metabolites and strain 23N1 is recommended as an effective bioremediation agent.

One-step synthesis of Cu(II) metal-organic gel as recyclable material for rapid, efficient and size selective cationic dyes adsorption.

Efficient removal of non-biodegradable and hazardous dyes from wastewater remains a hot research topic. Herein, a rationally designed a Cu(II)-based metal-organic gel (Cu-MOG) with a nanoporous 3D network structure prepared via a simple one-step mixing method was successfully employed for the removal of cationic dyes. The Cu-MOG exhibited high efficiency, with an adsorption capacity of up to 650.32 mg/g, and rapid adsorption efficiency, with the ability to adsorb 80% of Neutral Red within 1 min. The high adsorption efficiency was attributed to its large specific surface area, which enabled it to massively bind cationic dyes through electrostatic interaction, and a nanoporous structure that promoted intra-pore diffusion. Remarkably, the Cu-MOG displayed size-selective adsorption, based on adsorption studies concerning dyes of different sizes as calculated by density functional theory. Additionally, the adsorption performance of the Cu-MOG still maintained removal efficiency of 100% after three regeneration cycles. These results suggested that the Cu-MOG could be expected to be a promising and competitive candidate to conveniently process wastewater.

Elimination of textile dyes using activated carbons prepared from vegetable residues and their characterization.

In this study, three mesoporous activated carbons prepared from vegetable residues were used to remove acid, basic, and direct dyes from aqueous solutions, and reactive and vat dyes from textile wastewater. Granular carbons obtained by chemical activation at 673 K with phosphoric acid from prickly pear peels (CarTunaQ), broccoli stems (CarBrocQ), and white sapote seeds (CarZapQ) were highly efficient for the removal of dyes. Adsorption equilibrium studies were carried out in batch systems and treated with Langmuir and Freundlich isotherms. The maximum adsorption capacities calculated from the Langmuir isotherms ranged between 131.6 and 312.5 mg/g for acid dyes, and between 277.8 and 500.0 mg/g for basic dyes at 303 K. Our objective in this paper was to show that vegetable wastes can serve as precursors for activated carbons that can be used for the adsorption of dyes. Specifically CarBrocQ was the best carbon produced for the removal of textile dyes. The color removal of dyes present in textile wastewaters was compared with that of a commercial powdered carbon, and it was found that the carbons produced using waste material reached similar efficiency levels. Carbon samples were characterized by bulk density, point of zero charge, thermogravimetric analysis, elemental analysis, Fourier transform infrared spectroscopy, scanning electron microscopy, methylene blue adsorption isotherms at 303 K, and nitrogen adsorption isotherms at 77 K (SBET). The results show that the activated carbons possess a large specific surface area (1025-1177 m(2)/g) and high total pore volume (1.06-2.16 cm(3)/g) with average pore size diameters between 4.1 and 8.4 nm. Desorption and regeneration tests were made to test the viability of reusing the activated carbons.

Deep Cleaning of Crystal Violet and Methylene Blue Dyes from Aqueous Solution by Dextran-Based Cryogel Adsorbents.

Polysaccharides have recently attracted growing attention as adsorbents for various pollutants, since they can be extracted from a variety of renewable sources at low cost. An interesting hydrophilic and biodegradable polysaccharide is dextran (Dx), which is well-known for its applications in the food industry and in medicine. To extend the application range of this biopolymer, in this study, we investigated the removal of crystal violet (CV) and methylene blue (MB) dyes from an aqueous solution by Dx-based cryogels using the batch technique. The cryogel adsorbents, consisting of cross-linked Dx embedding a polyphenolic (PF) extract of spruce bark, were prepared by the freeze-thawing approach. It was shown that the incorporation of PF into the Dx-based matrix induced a decrease in porosity, pore sizes and swelling ratio values. Moreover, the average pore sizes of the DxPF cryogels loaded with dyes further decreased from 42.30 ± 7.96 µm to 23.68 ± 2.69 µm, indicating a strong interaction between the functional groups of the cryogel matrix and those of the dye molecules. The sorption performances of the DxPF adsorbents were evaluated in comparison to those of the Dx cryogels and of the PF extract. The experimental sorption capacities of the DxPF cryogel adsorbents were higher in comparison to those of the Dx cryogels and the PF extract. The DxPF cryogels, particularly those with the highest PF contents (sample DxPF2), demonstrated sorption capacities of 1.2779 ± 0.0703 mmol·g-1, for CV, and 0.3238 ± 0.0121 mmol·g-1, for MB. The sorption mechanisms were analyzed using mathematical models, including Langmuir, Freundlich, Sips and Dubinin-Radushkevich isotherms, and kinetic models, like pseudo-first-order (PFO), pseudo-second-order (PSO), Elovich and intra-particle diffusion (IPD). The sorption process was best described by the Sips isotherm and PSO kinetic models, indicating chemisorption as the dominant mechanism. This study outlines the importance of developing advanced renewable materials for environmental applications.

Advances in Nanohybrid Membranes for Dye Reduction: A Comprehensive Review.

Separating valuable materials such as dyes from wastewater using membranes and returning them to the production line is a desirable environmental and economical procedure. However, sometimes, besides filtration, adsorption, and separation processes, pollutant destruction also can be suitable using photocatalytic membranes. The art of producing nanohybrid materials in contrast with nanocomposites encompasses nanomaterial synthesis as a new product with different properties from raw materials for nanohybrids versus the composition of nanomaterials for nanocomposites. According to the findings of this research, confirming proper synthesis of nanohybrid is one challenge that can be overcome by different analyses, other researchers' reports, and the theoretical assessment of physical or chemical reactions. The application of organic-inorganic nanomaterials and frameworks is another challenge that is discussed in the present work. According to the findings, Nanohybrid Membranes (NHMs) can achieve 100% decolorization, but cannot eliminate salts and dyes, although the removal efficiency is notable for some salts, especially divalent salts. Hydrophilicity, antifouling properties, flux, pressure, costs, usage frequency, and mechanical, chemical, and thermal stabilities of NHMs should be considered.

Investigation on novel chitin and chitosan from dung beetle Heteronitis castelnaui (Harold, 1865) and its potential application for organic dyes removal from aqueous solution.

Chitosan, a natural polysaccharide, has attracted considerable attention as an environmentally friendly and highly efficient adsorbent for dye removal. It is usually produced by deacetylation or partial deacetylation of chitin. However, conventional sources of chitin and chitosan are limited, prompting the need for alternative sources with improved adsorption capabilities. Herein, this study focuses on exploring a novel chitin and chitosan source derived from the dung beetle and evaluates its potential for organic dye removal from aqueous solutions. The research involves the extraction and characterization of chitin and chitosan from dung beetle Heteronitis castelnaui (Harold, 1865) using various analytical techniques, including SEM, FT-IR, TGA, XRD, NMR, deacetylation degree and elemental analysis. The chitosan obtained was used for the formation of hydrogels with sodium alginate via cross-linking with calcium chloride. And then the prepared hydrogels were evaluated for its adsorption capacity through batch adsorption experiments using methylene blue as a model pollutant. The adsorption capacity for methylene blue was 1294.3 mg/g at room temperature with solution pH = 12, MB concentration of 1800 mg/L. Furthermore, the kinetics of the adsorption process were analyzed using pseudo-first-order and pseudo-second-order models to understand the rate of adsorption. The maximum adsorption capacities were determined using Langmuir and Freundlich isotherm models. This study provides valuable insights for the development of sustainable dye adsorption technologies, specifically investigating a novel chitosan source derived from the dung beetle.

Fabrication of maleic anhydride-acrylamide copolymer based sodium alginate hydrogel for elimination of metals ions and dyes contaminants from polluted water.

The study explores the synergy of biobased polymers and hydrogels for water purification. Polymer nanomaterial's, synthesized by combining acrylamide copolymer with maleic anhydride, were integrated into sodium alginate biopolymer using an eco-friendly approach. Crosslinking agents, calcium chloride and glutaraladehyde, facilitated seamless integration, ensuring non-toxicity, high adsorption performance, and controlled capacity. This innovative combination presents a promising solution for clean and healthy water supplies, addressing the critical need for sustainable environmental practices in water purification. In addition, the polymer sodium alginate hydrogel (MAH@AA-P/SA/H) underwent characterization via the use of several analytical procedures, such as FTIR, XPS, SEM, EDX and XRD. Adsorption studies were conducted on metals and dyes in water, and pollutant removal methods were explored. We investigated several variables (such as pH, starting concentration, duration, and absorbent quantity) affect a material's capacity to be adsorbed. Moreover, the maximum adsorption towards Cu2+ is 754 mg/g while for Cr6+ metal ions are 738 mg/g, while the adsorption towards Congo Red and Methylene Blue dye are 685 mg/g and 653 mg/g correspondingly, within 240 min. Adsorption results were further analyzed using kinetic and isothermal models, which showed that MAH@AA-P/SA/H adsorption is governed by a chemisorption process. Hence, the polymer prepared from sodium alginate hydrogel (MAH@AA-P/SA/H) has remarkable properties as a versatile material for the significantly elimination of harmful contaminants from dirty water.

Efficient removal of high concentration dyes from water by functionalized in-situ N-doped porous biochar derived from waste antibiotic fermentation residue.

Using biochar for dye wastewater treatment is attracting interest due to its excellent adsorption properties and low costs. In this work, a novel biochar derived from oxytetracycline fermentation residue (functionalized OFR biochar, FOBC) was investigated as a efficient adsorbent for typical dyes removal. At 25 °C, the maximum adsorption capacity calculated by Langmuir model of FOBC-3-600 for methylene blue (MB), malachite green (MG), and methyl orange (MO) reached 643.97, 617.89, and 521.03 mg/g, respectively. The kinetics and isotherm model fitting showed that the chemisorption and physisorption both occurred during the adsorption process. Dyes were efficiently adsorbed through pore filling, electrostatic attraction, π-π interactions, and surface complexation. And the cycling experiment and environmental risk assessment indicated that the FOBC-3-600 had excellent recyclability and utilization safety. Overall, this study provides a practical method to simultaneously treat the dyeing wastewater and utilize the antibiotic fermentation residue.

Structural properties and adsorption performance relationship towards three categories of lignin and their derived biochar.

The growing interest in utilizing lignin for dye removal has gained momentum, but there is limited information on the intricate relationship between lignin structural characteristics and adsorption efficacy, especially for its biochar derivatives. This study focused on three types of lignin and their corresponding biochar derivatives. Among them, ZnCl2-activated acidic/alkali densified lignin preparation of lignin-derived active carbon exhibited superior adsorption performance, achieving 526.32 mg/g for methylene blue and 2156.77 mg/g for congo red. Its exceptional adsorption capacity was attributed to its unique structural properties, including low alkyl and O-alkyl group content and high aromatic carbon levels. Furthermore, the adsorption mechanisms adhered to pseudo-second-order kinetics and the Langmuir model, signifying a spontaneous process. Intriguingly, lignin-derived active carbon also demonstrated remarkable recovery capabilities. These findings provide valuable insights into the impact of structural attributes on lignin and its biochar's adsorption performance.

Comparison of Oil-Seed Shell Biomass-Based Biochar for the Removal of Anionic Dyes-Characterization and Adsorption Efficiency Studies.

This research investigated the synthesis of biochar through the direct pyrolysis of pre-roasted sunflower seed shells (SFS) and peanut shells (PNS) and compared their application for the effective removal of textile dyes from wastewater. Biochar prepared at 900 °C (SFS900 and PNS900) showed the highest adsorption capacity, which can be attributed to the presence of higher nitrogen content and graphite-like structures. CHNS analysis revealed that PNS900 exhibited an 11.4% higher carbon content than SFS900, which enhanced the environmental stability of PNS biochar. Fourier-transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) analyses of the produced biochar indicated the degradation of cellulosic and lignin moieties. X-ray photoelectron spectroscopy (XPS) revealed a 13.8% and 22.6% increase in C-C/C=C mass concentrations in the SFS900 and PNS900, respectively, and could be attributed to the condensation of polyaromatic structures. Batch experiments for dye removal demonstrated that irrespective of dye species, PNS900 exhibited superior dye removal efficiency compared to SFS900 at similar dosages. In addition to H-bonding and electrostatic interactions, the presence of pyridinic-N and graphitic-N can play a vital role in enhancing Lewis acid-base and π-π EDA interactions. The results can provide valuable insights into the biochar-dye interaction mechanisms.

Efficient and Selective Removal of Heavy Metals and Dyes from Aqueous Solutions Using Guipi Residue-Based Hydrogel.

The presence of organic dyes and heavy metal ions in water sources poses a significant threat to human health and the ecosystem. In this study, hydrogel adsorbents for water pollution remediation were synthesized using Guipi residue (GP), a cellulose material from Chinese herbal medicine, and chitosan (CTS) through radical polymerization with acrylamide (AM) and acrylic acid (AA). The characteristics of the hydrogels were analyzed from a physicochemical perspective, and their ability to adsorb was tested using model pollutants such as Pb2+, Cd2+, Rhodamine B (RhB), and methyl orange (MO). The outcomes revealed that GP/CTS/AA-co-AM, which has improved mechanical attributes, effectively eliminated these pollutants. At a pH of 4.0, a contact duration of 120 min, and an initial concentration of 600 mg/L for Pb2+ and 500 mg/L for Cd2+, the highest adsorption capabilities were 314.6 mg/g for Pb2+ and 289.1 mg/g for Cd2+. Regarding the dyes, the GP/CTS/AA-co-AM hydrogel displayed adsorption capacities of 106.4 mg/g for RhB and 94.8 mg/g for MO, maintaining a stable adsorption capacity at different pHs. Compared with other competitive pollutants, GP/CTS/AA-co-AM demonstrated a higher absorption capability, mainly targeted toward Pb2+. The adsorption processes for the pollutants conformed to pseudo-second-order kinetics models and adhered to the Langmuir models. Even after undergoing five consecutive adsorption and desorption cycles, the adsorption capacities for heavy metals and dyes remained above 70% and 80%. In summary, this study effectively suggested the potential of the innovative GP/CTS/AA-co-AM hydrogel as a practical and feasible approach for eliminating heavy metals and dyes from water solutions.