Adsorptive removal of bulky dye molecules from water with mesoporous polyaniline-derived carbon.
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ABSTRACT:
SUBMITTER: An HJ
PROVIDER: S-EPMC7155913 | biostudies-literature |
REPOSITORIES: biostudies-literature
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Project description:Currently, a serious threat for living organisms and human life in particular, is water contamination with persistent organic and inorganic pollutants. To date, several techniques have been adopted to remove/treat organics and toxic contaminants. Adsorption is one of the most effective and economical methods for this purpose. Generally, porous materials are considered as appropriate adsorbents for water purification. Conventional adsorbents such as activated carbons have a limited possibility of surface modification (texture and functionality), and their adsorption capacity is difficult to control. Therefore, despite the significant progress achieved in the development of the systems for water remediation, there is still a need for novel adsorptive materials with tunable functional characteristics. This review addresses the new trends in the development of new adsorbent materials. Herein, modern carbon-based materials, such as graphene, oxidized carbon, carbon nanotubes, biomass-derived carbonaceous matrices-biochars as well as their composites with metal-organic frameworks (MOFs) and MOF-derived highly-ordered carbons are considered as advanced adsorbents for removal of hazardous organics from drinking water, process water, and leachate. The review is focused on the preparation and modification of these next-generation carbon-based adsorbents and analysis of their adsorption performance including possible adsorption mechanisms. Simultaneously, some weak points of modern carbon-based adsorbents are analyzed as well as the routes to conquer them. For instance, for removal of large quantities of pollutants, the combination of adsorption and other methods, like sedimentation may be recommended. A number of efficient strategies for further enhancing the adsorption performance of the carbon-based adsorbents, in particular, integrating approaches and further rational functionalization, including composing these adsorbents (of two or even three types) can be recommended. The cost reduction and efficient regeneration must also be in the focus of future research endeavors. The targeted optimization of the discussed carbon-based adsorbents associated with detailed studies of the adsorption process, especially, for multicomponent adsorbate solution, will pave a bright avenue for efficient water remediation.
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Project description:Current research mainly focuses on the reduction of adsorbable organic halogen (AOX) sources, while studies on AOX monitoring and management in the environment are scarce. Organic pollutants in water are mainly fixed by sediments. Thus, in this paper, activated carbon was used to simulate the adsorption of AOX by sediments. AOX volatilization and degradation were also studied to exclude their effect on adsorption. Micromolecule chlorides were more easily volatilized and degraded than chlorobenzene and chlorophenol. The adsorption of activated carbon to AOX in bleaching wastewater was also studied and the optimum conditions for AOX removal were elucidated (particle size, 62 µm; time, 120 min; pH, 2.5; temperature, 40°C; and activated carbon dosage, 1.75 g l-1). AOX adsorption by activated carbon is a chemical process. Hence, the chemical compositions of the bleaching effluent with and without adsorption were analysed by GC-MS. The results revealed that activated carbon exhibits a good AOX removal effect, thereby providing a theoretical basis for monitoring the AOX distribution in the environment.
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Project description:The electrochemical property of ordered mesoporous carbon (OMC) can be changed significantly due to the incorporating of electron-donating heteroatoms into OMC. Here, we demonstrate the successful fabrication of nitrogen-doped ordered mesoporous carbon (NOMC) materials to be used as carbon substrates for loading polyaniline (PANI) by in situ polymerization. Compared with NOMC, the PANI/NOMC prepared with a different mass ratio of PANI and NOMC exhibits remarkably higher electrochemical specific capacitance. In a typical three-electrode configuration, the hybrid has a specific capacitance about 276.1 F/g at 0.2 A/g with a specific energy density about 38.4 Wh/kg. What is more, the energy density decreases very slowly with power density increasing, which is a different phenomenon from other reports. PANI/NOMC materials exhibit good rate performance and long cycle stability in alkaline electrolyte (~?80% after 5000 cycles). The fabrication of PANI/NOMC with enhanced electrochemical properties provides a feasible route for promoting its applications in supercapacitors.
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Project description:The development of reliable production routes for sustainable hydrogen (H2), which is an essential feedstock for industrial processes and energy carrier for fuel cells, is needed. It appears to be an unavoidable alternative to significantly reduce the dependence on conventional energy sources based on fossil fuels without increasing the atmospheric CO2 levels. Among the different power-to-X scenarios to access high purity H2, the electrochemical approach based on electrolysis looks to be a promising sustainable solution at both the small and large industrial scales. However, the practical realization of this important opportunity faces several challenges, including the efficient design of cost-effective catalytic materials to be used as a cathode with improved intrinsic and durable activity. In this contribution, we report the design and development of efficient nanostructured catalysts for the electrocatalytic hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in aqueous media, whereby noble metal-free elements are embedded in a matrix of a conducting polymer, polyaniline (PANI). To increase the electrical conductivity and further the electrocatalytic ability toward HER of the chemically polymerized PANI in the presence of nickel (II) salt (nitrate), the PANI-based materials have first been stabilized at a mild temperature of 250-350°C in air and then carbonized at 800-1,000°C under nitrogen gas to convert the chemical species into nitrogen, sulfur, nickel, and carbon nanostructured networks (CNNs). Different physicochemical (TGA-DSC, Raman spectroscopy, XRD, SEM, EDX, ICP, CHNS, BET, and XPS) and electrochemical (voltammetry and electrochemical impedance spectrometry) methods have been integrated to characterize the as-synthesized CNNs materials and interrogate the relationship of material-to-performance. It has been found that those synthesis conditions allow for the substantial increase of the electrocatalytic performance toward HER and OER in alkaline media in terms of the onset potential and charge transfer resistance and overpotential at the specific activity of 10 milliamps per square centimeter, thus ranking the present materials among the most efficient noble metal-free catalysts and making them possible candidates for integration in practical low-energy consumption alkaline electrolyzers.
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Project description:Background and aimFinding a cost-effective adsorbent can be an obstacle to large-scale applications of adsorption. This study used an efficient activated carbon adsorbent based on agro-waste for dye removal.MethodsPistachio shells as abundant local agro-wastes were used to prepare activated carbon. Then, it was modified with iron to improve its characteristics. Acid red 14 was used as a model dye in various conditions of adsorption (AR14 concentration 20-150 mg L-1, pH 3-10, adsorbent dosage 0.1-0.3 g L-1, and contact time 5-60 min).ResultsA mesoporous adsorbent was prepared from pistachio shells with 811.57 m2 g-1 surface area and 0.654 cm3 g-1 pore volume. Iron modification enhanced the characteristics of activated carbon (surface area by 33.3% and pore volume by 64.1%). Adsorption experiments showed the high effectiveness of iron-modified activated carbon for AR14 removal (>99%, >516 mg g-1). The adsorption followed the pseudo-second kinetic model (k = 0.0005 g mg-1 min-1) and the Freundlich isotherm model (Kf = 152.87, n = 4.61). Besides, the reaction occurred spontaneously (ΔG0 = -36.65 to -41.12 kJ mol-1) and was exothermic (ΔH0 = -41.86 kJ mol-1 and ΔS0 = -3.34 J mol-1 K-1).ConclusionIron-modified activated carbon derived from pistachio shells could be cost-effective for the treatment of industrial wastewater containing dyes.
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Project description:In the presence of melamine and block copolymers, namely, F108, F127, and P123, nitrogen-doped nanoporous carbon nanospheroids (N@CNSs) were synthesized by the hydrothermal process. The F127-modified sample (CNF127) exhibits the maximum Brunauer-Emmett-Teller (BET) surface area of 773.4 m2/g with a pore volume of 0.877 cm3/g. The microstructural study reveals that nanospheroids of size 50-200 nm were aggregated together to form a chainlike structure for all triblock copolymer-modified samples. The X-ray photoelectron spectroscopy study shows the binding energies of 398.33 and 400.7 eV attributed to sp2 (C-N=C)- and sp3 (C-N)-hybridized nitrogen-bonded carbons, respectively. The synthesized N@CNS samples showed selective adsorption of organic dye methylene blue (MB) in the presence of methyl orange (MO) as well as Pb(II) ion removal from contaminated water. The adsorptions for MB and Pb(II) ions followed pseudo-first-order and pseudo-second-order kinetic models, respectively. The sample CNF127 showed the highest adsorption of 73 and 99.82 mg/g for MB and Pb(II) adsorptions, respectively. The adsorption capacity for MB of the copolymer-modified samples follows the order CNF127 > CNP123 > CNF108, which corroborated with the mesoporosity as well as nitrogen content of the corresponding samples. The maximum % adsorption of Pb(II) follows the order CNF127 (99.82%) > CNF108 (98.74%) > CNP123 (91.82%), and this trend is attributed to the BET surface area of the corresponding samples. This study demonstrates multicomponent removal of water pollutants, both organic dyes and inorganic toxic metal ions.
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Project description:The present study investigated the adsorptive and enzymatic removal of aniline blue dye (AB) from aqueous solution using waxy riceprocessing waste (RW), peanut shell (PS), microbial waste of Aspergillus niger (MW) as low cost adsorbents, and laccase (Lac) as a biocatalyst. Commercial activated carbon (AC) was also employed to compare the adsorption performance with the three adsorbents. Dye removal was examined under various parameters in batch experiments. It was found that dye removal by RW and Lac was 89?94% noticeably better than that by MW and PS (20?70%). In any cases, AC produced the highest dye removal among the tested materials. The kinetics, isotherms, and thermodynamics were then analyzed to elucidate the adsorption process by the four adsorbents. The pseudo-second order kinetic was superior to the pseudo first order kinetic model in describing adsorption for all adsorbents. The Langmuir model fitted the adsorption process very well, indicating monolayer coverage of dyes on a solid surface. A thermodynamic analysis of enthalpy (?H°), entropy (?S°), and Gibbs free energy (?G°) classified the adsorption as a nonspontaneous and endothermic process. The results reveal diverse natural materials (e.g., processing waste RW) as novel substitutes for traditional activated carbon, as well as laccase as a green catalyst for the treatment of dye wastewater.
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Project description:Hybrid ion exchangers (HIX) containing manganese(IV) oxide (MnO2) based on macroporous and gel-type carboxylic cation exchangers as supporting materials were obtained. The hybrid materials were characterized using scanning electron microscopy with energy dispersive spectrometry (SEM/EDS), Fourier transform infrared spectroscopy (FTIR), X-ray powder diffraction (XRD) and nitrogen adsorption isotherms at 77 K and mercury porosimetry. HIX with introduced MnO2 (20.0-32.8 wt% Mn) were tested for removal of dissolved sulfides from anoxic aqueous solutions with 100-500 mg S2-/dm3 concentrations. The process proceeded effortlessly at pH 10-13 despite unfavorable electrostatic interactions of the reactants. The highest exhibited sorption capacity was 144.3 ± 7.1 mg S2-/g. Approximately 65% of dissolved sulfides were oxidized to S2O32- ions and repelled from HIX structure. On average, 13% of sulfide removal products were adsorbed by the MnO2 surface. The impact of MnO2 load and the ionic form of HIX functional groups on removal of sulfides and resulting products was examined. The mechanism of the process is suggested.
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Project description:Valorization of agri-food organic waste in order to reach zero waste using cleaner methods is still a challenge. Therefore, both anaerobic co-digestion (ACD) (biological process) and adsorption (physicochemical process) were used in combination for this objective. ACD allows the activation of biodegradable organic matter by microbial action and produces a digestate (co-product). This coproduct was used as a raw material to produce porous carbon having a high specific surface area after chemical treatment using sulfuric acid and thermal activations at temperature T = 350 °C. The resulted material was used for the preparation of core-shell particles with a core made of porous carbon and a shell consisting mainly of alginate and a calcium ion layer. The final core-shell particles were then used for dye treating wastewater and solving the solid-liquid separation problem in the adsorption process. We show here that in the ACD process, significant bio-methane potential (BMP) was produced. Furthermore, the data indicate that 153 L CH4 kg·SV-1 of BMP was produced under optimum conditions of pH = 8 and inoculum/load ratio = 1.2. The overall results concerning the methylene blue (MB) adsorption from water onto the core-shell particles show the occurrence of a maximum adsorbed amount equal to 26.178 mg g-1, and good agreement was found between the experimental adsorption data with pseudo-second-order and Langmuir theoretical models. The response surface methodology coupled with the central composite design has allowed the identification of optimal conditions for MB removal and has led to the elucidation of adsorption mechanism and the regeneration of the adsorbent without the occurrence of the solid/liquid separation problem.
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