Remediation of PFAS-impacted soils using magnetic activated carbon (MAC) and hydrothermal alkaline treatment (HALT).

Per- and polyfluoroalkyl substances (PFAS) are a group of synthetic pollutants that are bioaccumulative, toxic, and persistent. One long-term source for PFAS release is PFAS-contaminated soil. Addition of activated carbon (AC) to soil has shown the potential to immobilize PFAS and reduce PFAS bioavailability, but PFAS-loaded spent AC remaining in the treated soil could lead to remobilization. Here we report a novel approach to address this challenge. By applying magnetic activated carbon (MAC) to remediate PFAS-impacted soil, the PFAS-loaded MAC can be retrieved from the treated soil and sorbed PFAS in the spent MAC can be destroyed using hydrothermal alkaline treatment (HALT). Effective MAC recovery was observed when water/soil ratios (w/w) were either <0.07 or > 1. Soil organic content and pH affected PFAS adsorption by the MAC added to soil. After three months of incubation with MAC, high PFAS removals [PFOS (87.6 %), PFOA (83.8 %), and 6:2 FTSA (81.5 %)] were observed for acidic environmental sandy soils with low organic content. In contrast, PFAS removal by MAC was poor for garden soils with high organic matter content. MAC was also used to remediate aqueous film-forming foam (AFFF)-impacted and PFAS-contaminated aged soils with varying PFAS removal performance. HALT technology was able to destroy and defluorinate PFAS adsorbed to the spent MAC. Additionally, the HALT-treated MAC retained its magnetic properties and PFOS sorption capacity, suggesting the potential reusability of HALT-treated MAC. Considering the low energy footprint of HALT compared to conventional PFAS thermal destruction techniques, the combination of MAC and HALT could be a promising treatment train for PFAS-contaminated soils.

Magnetic activated carbon from spent coffee grounds: iron-catalyzed CO2 activation mechanism and adsorption of antibiotic lomefloxacin from aqueous medium.

The facile fabrication of low-cost adsorbents possessing high removal efficiency and convenient separation property is an urgent need for water treatment. Herein, magnetic activated carbon was synthesized from spent coffee grounds (SCG) by Fe-catalyzed CO2 activation at 800 °C for 90 min, and magnetization and pore formation were simultaneously achieved during heat treatment. The sample was characterized by N2 adsorption-desorption, XRD, VSM, SEM, and FTIR. Batch adsorption experiments were conducted using lomefloxacin (LMO) as the probing pollutant. Preparation mechanism was revealed by TG-FTIR and XRD. Experimental results showed that Fe3O4 derived from Fe species can be reduced to Fe by carbon at high temperatures, followed by subsequent reoxidation to Fe3O4 by CO2, and the redox cycle between Fe and Fe3O4 favored the formation of pores. The promotion effects of Fe species on CO2 activation can be quantitatively reflected by the yield of CO as the signature gaseous product, and the suitable activation temperate range was determined to be 675 to 985 °C. The BET surface area, total pore volume, and saturated magnetization value of the product were 586 m2 g-1, 0.327 cm3 g-1, and 11.59 emu g-1, respectively. The Langmuir model was applicable for the adsorption isotherm data for LMO with the maximum adsorption capacity of 95 mg g-1, and thermodynamic analysis revealed that the adsorption process was endothermic and spontaneous. This study demonstrated that Fe-catalyzed CO2 activation was an effective method of converting SCG into magnetic separable adsorbent for LMO removal from aqueous medium.

[Removal of Cr(â ¥) via a Nickel Ferrite@Activated Carbon Composite Under Batch Experiments: Study of Characterization, Performance, and Mechanism].

A magnetic activated carbon adsorbent named NiFe2O4@AC was synthesized by modifying activated carbon with NiFe2O4 and used for the adsorption of Cr(Ⅵ) ions from waste water. The influencing factors, adsorption kinetics, and adsorption isotherms of Cr(Ⅵ) adsorption by the adsorbent were investigated. The results showed that the removal rate of Cr(Ⅵ) adsorption by NiFe2O4@AC reached 96.92%, and the adsorption amount reached 72.62 mg·g-1 at the adsorption conditions of temperature (298 K), pH 2, Cr(Ⅵ) initial concentration (150 mg·L-1), adsorbent dosage (0.1 g), and contact time (720 min). The experimental data were best described by the proposed secondary kinetics and Langmuir model, indicating that the adsorption process was a monolayer chemisorption process. The increase in temperature favored the adsorption of Cr(Ⅵ) on NiFe2O4@AC because the adsorption process was a spontaneous, heat-absorbing reaction. The adsorption mechanism of NiFe2O4@AC was mainly through complexation and electrostatic attraction to adsorb Cr(Ⅵ); meanwhile, the applied magnetic field could be separated from the solution, which has good application prospects.

2,4-Dichlorophenoxyacetic acid (2,4-D) adsorptive removal by algal magnetic activated carbon nanocomposite.

In the present study, ferric oxide nanoparticles impregnated with activated carbon from Ulva prolifera biomass (UPAC-Fe2O3) were prepared and employed to remove 2,4-Dichlorophenoxyacetic acid (2,4-D) by adsorption. The UPAC-Fe2O3 nanocomposite was characterized for its structural and functional properties by a variety of techniques. The nanocomposite had a jagged, irregular surface with pores due to uneven scattering of Fe2O3 nanoparticles, whereas elemental analysis portrayed the incidence of carbon, oxygen, and iron. XRD analysis established the crystalline and amorphous planes corresponding to the iron oxide and carbon phase respectively. FT-IR analyzed the functional groups that confirmed the integration of Fe2O3 nanoparticles onto nanocomposite surfaces. VSM and XPS studies uncovered the superparamagnetic nature and presence of carbon and Fe2O3, respectively, in the UPAC-Fe2O3 nanocomposite. While the surface area was 292.51 m2/g, the size and volume of the pores were at 2.61 nm and 0.1906 cm3/g, respectively, indicating the mesoporous nature and suitability of the nanocomposites that could be used as adsorbents. Adsorptive removal of 2,4-D by nanocomposite for variations in process parameters like pH, dosage, agitation speed, adsorption time, and 2,4-D concentration was studied. The adsorption of 2,4-D by UPAC-Fe2O3 nanocomposite was monolayer chemisorption owing to Langmuir isotherm behavior along with a pseudo-second-order kinetic model. The maximum adsorption capacity and second order rate constant values were 60.61 mg/g and 0.0405 g/mg min respectively. Thermodynamic analysis revealed the spontaneous and feasible endothermic adsorption process. These findings confirm the suitability of the synthesized UPAC-Fe2O3 nanocomposite to be used as an adsorbent for toxic herbicide waste streams.

Dynamic adsorption of diclofenac onto a magnetic nanocomposite in a continuous stirred-tank reactor.

In this study, a waste-based magnetic activated carbon (MAC) was used for the first time in a continuous-flow stirred tank reactor (CSTR). The aim was to evaluate the dynamic removal of diclofenac (DCF) from water and wastewater. Firstly, the breakthrough curves corresponding to DCF adsorption from distilled water at different feed flow rates and doses of MAC were determined. After selecting the most favourable conditions, namely 0.18 h L-1 flow rate and 400 mg L-1 of MAC, the effect of different aqueous matrices was studied, with the breakthrough curves evidencing a performance decline in wastewater in comparison with distilled water. Finally, the exhausted MAC was magnetically recovered, regenerated by microwave-assisted heating and applied in two subsequent adsorption cycles. The regeneration studies pointed to a decrease of the specific surface area and an improvement of the magnetic retrievability of MAC. After the first regeneration step, just mild effects were observed in the dynamic adsorptive performance of MAC. However, after a second regeneration step, the performance declined ca. 50%. Overall, the results highlight the feasibility of producing waste-based magnetic composites that simultaneously combine high adsorption efficiency under dynamic operation in a CSTR, with easy retrievability and successful one-stage regeneration for further reutilization.

Adsorption of As(III) and As(V) from aqueous solution by magnetic biosorbents derived from chemical carbonization of pea peel waste biomass: Isotherm, kinetic, thermodynamic and breakthrough curve modeling studies.

The purpose of this research was to investigate the adsorption of arsenic (As) from aqueous solutions using MPAC-500 and MPAC-600 (magnetic-activated carbons synthesized from the peel of Pisum sativum (pea) pyrolyzed at 500 °C and 600 °C temperatures, respectively). The potential of both biosorbents for As adsorption was determined in batch and column mode. The characterization of both biosorbents was performed by energy dispersive spectroscopy, scanning electron microscope, pHZPC, particle size distribution, X-ray diffraction, zeta potential and Fourier-transform infrared spectroscopy. It was found that the efficiency of MPAC-600 was better than MPAC-500 for the adsorption of As(III) and As(V) ions. The adsorption capacities of MPAC-500 and MPAC-600 in removing As(III) were 0.7297 mg/g and 1.3335 mg/g, respectively, while the values of Qmax for As(V) on MPAC-500 and MPAC-600 were 0.4930 mg/g and 0.9451 mg/g, respectively. The Langmuir isotherm model was found to be the best fit for adsorption of As(III) by MPAC-500 and MPAC-600, as well as adsorption of As(V) by MPAC-500. The Freundlich isotherm model, on the other hand, was optimal for As(V) removal with MPAC-600. With R2 values close to unity, the pseudo-second-order kinetics were best fitted to the adsorption process of both As species. The Thomas model was used to estimate the breakthrough curves. The effects of coexisting oxyanions and regeneration studies were also carried out to examine the influence of oxyanions on As adsorption and reusability of biosorbents.

Food industrial biowaste-based magnetic activated carbons as sustainable adsorbents for anthropogenic mercury emissions.

Bio-derived magnetic activated carbons from industrial chestnut shell waste have been obtained through a novel, optimized and sustainable methodology where impregnation, pyrolysis, acid washing or other intermediate steps commonly used in the activation process were eliminated saving time, energy and costs. The resulting materials (MACs) were obtained at 220-800 °C showed interesting properties: textural (SBET up to 568 m2 g-1) and magnetic (different iron species developed), depending on the activation temperature employed. Data showed outstanding results when MACs were tested for Hg removal in pollution emissions at 150 °C in lab-scale device. In MACs obtained at 500-600 °C, where the highest concentration of magnetite was found, the best Hg adsorption capacity was achieved, while it decreased when metallic iron or iron carbides were present (MACs obtained at 800 °C). Moreover, the difference of Hg0 removal/adsorption in N2+O2 and Simulated Flue Gas atmosphere between MACs obtained at 500 and 600 °C pointed out the influence on Hg removal of additional parameters, as surface chemistry and the existence of sulfur or chloride. The determination of Hg species in post-retention solids confirmed the mercury oxidation by high-valence iron ions (Fe3+) and the involvement of physisorption and chemisorption processes for the gas-solid interaction mechanism.

A comparative study on adsorption behavior of iodinated X-ray contrast media iohexol and amidotrizoic acid by magnetic-activated carbon.

As persistent and ubiquitous contaminants in water, iodinated X-ray contrast media (ICM) pose a non-negligible risk to the environment and human health. In this study, we investigated the adsorption behavior of two typical ICM compounds, iohexol (IOH) and amidotrizoic acid (DTZ), on magnetic activated carbon. Theoretical investigations, using density functional theory, identified the molecule structures and calculated the molecular diameters of IOH (1.68 nm) and DTZ (1.16 nm), which revealed that ICM could be adsorbed by mesopores and larger micropores. Therefore, magnetic activated carbon with a porous structure was prepared by the co-precipitation method to investigate the adsorption mechanism of IOH and DTZ. MAC--5 (magnetic activated carbon with a theoretical iron oxide content of 37%) showed the best adsorption ability for both IOH and DTZ, with maximum adsorption capacities of 86.05 and 43.00 mg g-1, respectively. Adsorption kinetics and isotherm models were applied to explore the mechanisms involved, and the effects of solution pH, initial concentration, temperature, ionic strength, and natural organic matter were also investigated. The pore filling effect, π-π stacking, hydrogen bonding, and electrostatic interaction, were found to be the main adsorption mechanisms. The co-adsorption data showed that competition may occur in ICM coexisting environments. Interestingly, the used MAC--5 could be successfully regenerated and its adsorption efficiency did not decrease significantly after five cycles, indicating that it is a promising adsorbent for ICM. The results from this study provide some new insights for the treatment of water containing ICM.

Effect of UVC and UVA Photocatalytic Processes on Tetracycline Removal Using CuS-Coated Magnetic Activated Carbon Nanocomposite: A Comparative Study.

In this study, we synthesized a novel MAC nanocomposite using almond's green hull coated with CuS. The whole set of experiments have been conducted inside a batch (discontinuous reactor system) at room temperature. The effectiveness of different parameters in tetracycline removal pH (3, 5, 7, and 9), pollutant concentration (5-100 mg/L), nanocomposite dosage (0.025-1 g/L), and contact time (5-60 min) using newly synthesized nanocomposite were investigated. Based on the results, in the optimal conditions of pH = 9, nanocomposite dosage of 1 g/L, pollutant concentration of 20 mg/L, contact time of 60 min, and room temperature, 95% removal efficiency was obtained. In MAC/CuS/UVC process, the removal of COD and TOC were 76.89% and 566.84% respectively meanwhile, these values in MAC/CuS/UVA process were 74.19% and 62.11%, respectively. The results of nanocomposite stability and magnetic recovery illustrated that the removal efficiency was reduced by 1.5% in the presence of UVC and 5% in the presence of UVA lights during all six cycles. Therefore, this nanocomposite was highly capable of recycling and reuse. It can be concluded that considering the high potential of the synthesized nanocomposite, the photocatalytic efficiency of the MAC/CuS/UVC process in tetracycline synthesis was higher than MAC/CuS/UVA process.

Synthesis of the magnetic core-shell bi-metallic and tri-metallic metal-organic framework nanocomposites for dye adsorption.

Bi-metallic and tri-metallic metal-organic frameworks (MOFs) supported on the magnetic activated carbon (MAC) were synthesized for the reduction of methylene blue (MB) concentration in the aqueous solutions. The adsorbent nanocomposites were characterized by applying the general tests including XRD, FTIR, FESEM, TEM, BET, and VSM. The XRD achievements demonstrated that crystalline structure of MOFs was derived on the MAC by the presented method. The core-shell morphology with nano-scale size of the magnetic carbonaceous MOFs was detected in TEM and FESEM micro-images. The acceptable magnetic strength of the prepared adsorbents was proved by using the VSM analysis. The important operating conditions including pH and temperature were also evaluated, while the other parameters were kept constant. The pseudo-second-order kinetic model was matched with the experimental data to show the kinetic behavior of the multi-component MOFs. The isotherm studies showed that the good agreement between the experimental data with both Langmuir model and the maximum capacities was calculated to be about 66.51 and 71.43 mg/g for the bi-metallic and tri-metallic nanocomposites, respectively. Regeneration experiments indicated that the fabricated adsorbents have an excellent reusing adsorption capacity which can be a proper selection for the industrial applications. PRACTITIONER POINTS: Bi-metallic and tri-metallic MOFs supported on the magnetic activated carbon were synthesized by the facile preparation method. Adsorption of methylene blue by using MOFs were successfully done. Nanocomposites were evaluated by XRD, FTIR, BET, FESEM, TEM, and VSM techniques. Maximum of adsorption capacity was observed for tri-metallic MOF as 71.43 mg/g.

Synthesis and characterization of Ni-doped anatase TiO2 loaded on magnetic activated carbon for rapidly removing triphenylmethane dyes.

In this work, we employed the in situ synthesis method to implant Fe3O4 into activated carbon (AC), in which the synthesis of the magnetic AC (MAC) was realized. Thence, Ni-doped anatase TiO2 (NATiO2) were anchored on different addition amount of MAC to synthesize the series of Ni-TiO2/MAC photocatalysts. The chemical compositions and physical properties of these nanocomposites were analyzed by various characterization technologies. The photocatalytic capabilities of as-produced materials were then investigated via adsorption and photodegradation of triphenylmethane dyes (TPMs) as crystal violet (CV), basic fuchsine (BF), and malachite green (MG) solution. The results revealed that the removal of Ni-TiO2/AC, Ni-TiO2/2MAC, Ni-TiO2/4MAC, and Ni-TiO2/8MAC on TPMs is a very fast process and the removal efficiency can almost reach to about 90% in 10 min, and the catalyst has good cycle stability and is easy to be reused. This work provides a novel, low-cost, and effective way to rationally design and synthesize TiO2-based photocatalysts for effective removal of TPMs.

Unveiling the correlation of Fe3O4 fractions upon the adsorption behavior of sulfamethoxazole on magnetic activated carbon.

Magnetic particles (MPs) assisted powdered activated carbon (PAC) is a promising composite material for adsorption removal of micropollutants. The fractional amount of Fe3O4 impacts the balance between adsorption capacity and magnetic property of magnetic activated carbons (MPACs), and therefore it affects the extent of sulfamethoxazole (SMX) removal. Here, five MPACs with different mass ratios of Fe3O4: PAC (1:1, 1:2, 1:4, 1:6, and 1:8) were prepared using a hydrothermal method and characterized by various spectroscopic methods. The spherical shaped MPs were monolayerly deposited on PAC with fewer pores blocked when the mass ratio of Fe3O4 was comparatively low (≤ 20%). MPAC6 (14.3 wt% of Fe3O4) had the best overall performance, with good Langmuir adsorption capacities for SMX (173.0 mg g-1) and excellent magnetic properties (9.0 emu g-1). Corresponding adsorption kinetics fitted well with the pseudo second-order kinetic model. The negative ΔG0 (-25.6 to -27.2 KJ mol-1) and ΔH0 (-9.14 KJ mol-1), and positive ΔS0 (0.55 KJ mol-1 K-1) properties indicated the spontaneous and exothermic nature of the adsorption process accompanied by an increase in entropy. The strong cation-assisted electron donor-acceptor and hydrophobic interactions were contributed to a high extent of SMX removal in the pH range of 2-4. Formation of negative charge-assisted H-bonds was responsible for the adsorption of hydrophilic SMX- on negatively charged MPAC6 in alkaline solution. Desorption and regeneration experiments showed SMX removal was still 92.3% in the 5th cycle. These findings give valuable insights into the interactions between SMX and MPACs and guide for choosing sustainable magnetic adsorbents for environmental applications.

Enhanced optical properties and photocatalytic activity of TiO2 nanotubes by using magnetic activated carbon: evaluating photocatalytic reduction of Cr(VI).

In recent years, photocatalytic reduction of Cr(VI) to Cr(III) by TiO2 nanostructures, as a potent environmental technology has attracted a lot of attention. However, several defects including the large band gap energy of TiO2, fast photogenerated charge recombination and re-oxidation of Cr(III) restrict their practical application. In this work, the incorporation of TiO2 nanotubes (TNTs) with magnetic activated carbon (MAC) and photoreduction in the presence of a hole scavenger were studied as a preferable approach. The results revealed that coupling TNTs with 2 wt% MAC can boost the surface area from 89.54 to 307.87 m2 g-1 as well as decrease the band gap energy from 3.1 to 2.7 eV. As a consequence of the enhancement in textural features and optical properties, TNTs/MAC (2%) led to improvement of photoreduction efficiency (from 47% to 66%) in comparison with the TNTs. Meanwhile, the experiments demonstrated that using 0.2 g TNTs/MAC as an optimal dosage in acidic solution increases the photoreduction efficiency up to 81%. The hole scavenger investigation had a marvellous result. It was found that in the presence of oxalic acid, TNTs/MAC (2%) could reduce 97% of Cr(VI) which it was due to trapping oxidative species and charge-transfer-complex-mediated process. Furthermore, the kinetic study affirmed that the photoreduction follow first-order kinetics and the reaction rate constants by TNTs/MAC (2%) are 1.5 times as great as those of TNTs. Moreover, the reusability tests illustrated TNTs/MAC (2%) has good stability and is active even up to the six runs.

Utilization of Tires Waste-Derived Magnetic-Activated Carbon for the Removal of Hexavalent Chromium from Wastewater.

The present study focuses on fabrication of magnetic activated carbon (M-AC) using tire waste and its potential investigation for adsorption of Cr (VI) from wastewater. The composite material (M-AC) was synthesized by pyrolysis followed by in situ magnetization method, and characterized by FTIR, FESEM, EDX, and XRD analysis. The maximum adsorption of Cr (VI) ion over composite adsorbent was found (~99.5%) to occur at pH 2, sample volume 10 mL, adsorbent dose 100 mg, contact time 30 min. The adsorption process was endothermic, feasible, spontaneous, and was found to follow pseudo second order of the reaction. The Cr ion could be completely desorbed (~99.3%) from the composite adsorbent by using 20 mL of 2 M NaOH solution. The composite adsorbent was regenerated by continuous adsorption and desorption for 5 consecutive cycles by using 10 mL 0.1 M HCl solution. M-AC also performed well in case of tannery wastewater by removing about 97% of Cr (VI).

Single-step pyrolysis for producing magnetic activated carbon from tucumã (Astrocaryum aculeatum) seed and nickel(II) chloride and zinc(II) chloride. Application for removal of nicotinamide and propanolol.

The present research describes the synthesis of new nanomagnetic activated carbon material with high magnetization, and high surface area prepared in a single pyrolysis step that is used for the carbonization, activation, and magnetization of the produced material. The pyrolysis step of tucumã seed was carried out in a conventional tubular oven at 600 °C under N2-flow. It was prepared three magnetic carbons MT-1.5, MT-2.0, MT-2.5, that corresponds to the proportion of biomass: ZnCl2 always 1:1 and varying the proportion of NiCl2 of 1.5, 2.0, and 2.5, respectively. These magnetic nanocomposites were characterized by Vibrating Sample Magnetometer (VSM), X-ray diffraction, scanning electron microscopy, thermogravimetric analysis, hydrophobic/hydrophilic balance, CHN/O elemental analysis, modified Boehm titration, N2 adsorption-desorption isotherms; and pHpzc. All the materials obtained presented Ni particles with an average crystallite size of less than 33 nm. The MT-2.0 was employed for the removal of nicotinamide and propranolol from aqueous solutions. Based on Liu isotherm, the Qmax was 199.3 and 335.4 mg g-1 for nicotinamide and propranolol, respectively. MT-2.0 was used to treat simulated pharmaceutical industry effluents attaining removal of all organic compounds attaining up to 99.1 % of removal.

Magnetic activated carbon (MAC) mitigates contaminant bioavailability in farm pond sediment and dietary risks in aquaculture products.

Heavy metals (HMs) and polycyclic aromatic hydrocarbons (PAHs) are among the contaminants of concern in aquaculture ponds due to their frequent detection and high bioaccumulation in aquatic products and hence high dietary risks to human beings. In this study, magnetic activated carbon (MAC) was added as a stabilization and removal adsorbent to native pond sediment with known contamination of HMs and PAHs to reduce the tissue residues and dietary risks of HMs and PAHs in a model aquaculture species (Venerupis philippinarum) in the course of a 28-day bioaccumulation experiment. Meanwhile, passive sampling techniques based on diffusive gradient in thin films (DGT) and polydimethylsiloxane (PDMS) were applied to sense the bioavailable fraction of HMs and PAHs in sediment during the stabilization process. The results showed that 3% dosage of MAC to sediment achieved the most cost-effective stabilization for HMs and PAHs. A remarkable decrease was observed with the tissue residues of HMs and PAHs in V. philippinarum (28-47% for HMs and ~76% for ∑PAHs), which was quantitatively linked to the decline in their bioavailable concentrations in sediment pore water (31-46% for HMs and ~76% for ∑PAHs). Consequently, the target hazard quotients (THQs) posed by HMs and incremental lifetime cancer risks (ILCRs) by PAHs in V. philippinarum were reduced by 38% and 46%, respectively. Along with the magnetic recovery of ~70% MAC from the sediment, HMs (4.8-13%) and PAHs (2-60%) can be effectively removed. We further established a multi-domain equilibrium sorption model that was able to predict the optimal amendment of MAC for quantitative mitigation of bioavailable PAHs in sediment pore water within a certain range of MAC dosage. Future studies are warranted to explore the applicability domain of MAC for in situ remediation in aquaculture ponds to ensure the quality of farming organisms or to serve other purposes in aquatic systems.

Preparation, characterization, and application of magnetic activated carbon for treatment of biologically treated papermaking wastewater.

In view of the urgent need for tertiary treatment of papermaking wastewater and the difficulty in separating powdered activated carbon (PAC) from water, the magnetic activated carbon (33%-MPAC, 50%-MPAC and 67%-MPAC) were prepared by chemical coprecipitation method for adsorption of biologically treated papermaking wastewater (BTPW). A series of characterization of MPAC and PAC were carried out and show that the content of iron oxides is negatively related to the proportion of micropores in MPAC. The loaded iron oxides is mainly the mixture of magnetite and maghemite, and the maximum saturation magnetization of MPAC can reach 29.68 emu/g. Batch mode experiments were performed, and found that the adsorption effect of MPAC is slightly worse than that of PAC, the adsorption capacity of COD in MPAC can reach about 65 mg/g, and pH = 2 and 10 °C are more favorable for adsorption. The adsorption isotherms and kinetics were well fitted by the Freundlich model and pseudo-second-order kinetic model, respectively. The selective adsorption was studied by using the excitation emission matrix (EEM) fluorescence spectrum and high-performance size exclusion chromatography (HPSEC). It is concluded that all adsorbents are preferred to adsorb humic acid-like substances (HA). And all adsorbents are preferred to adsorb low apparent molecular weight substances (LAMW, AMW < 1500 Da), with the increase of iron oxides content, the phenomenon of MPAC preferentially adsorbed LAMW became less obvious.

Understanding reactions and pore-forming mechanisms between waste cotton woven and FeCl3 during the synthesis of magnetic activated carbon.

FeCl3 is a valuable iron salt used in the synthesis of magnetic waste cotton woven-based activated carbon. Although it has received extensive research attention, more information is required regarding its interactions with the carbon matrix. This systematic study describes the potential reactions of FeCl3 and waste cotton woven. First, the textural properties of waste cotton woven-based activated carbon synthesized under various conditions were investigated via element analysis, N2 sorption/desorption isotherms, and scanning electron microscopy. Then, the possible reaction mechanisms were deduced through various characterization methods. The results demonstrate that FeCl3 can lower the initial decomposition temperature of WCW to 135 °C and catalyze decarboxylation and decarbonylation at 100-330 °C to elevate the formation of microporous structures. Moreover, FeCl3 can also form Lewis acid sites at 330-700 °C and promote the cross-linking reaction to develop intricate microporous structures and carbonaceous materials with the synergistic effect of Fe3+ and Cl-. FeCl3 could be used as a template-like agent to form mesoporous structures. Meanwhile, it can also act as a magnetizer that Fe3O4 derived from the decomposition of FeCl3 would insert into the carbon matrix and combine with C-Cl to tailor the magnetic controllable activated carbon. Finally, we confirmed that extending the activation time could convert the structure of waste cotton woven-based activated carbon and increase the number of active sites, thereby further improving the catalytic properties of FeCl3 in pore formation.

Use of chicken feather and eggshell to synthesize a novel magnetized activated carbon for sorption of heavy metal ions.

Keeping environment and sustainability concept in view with preparation of new sorbents, two waste by-products from the poultry industry, i.e. feather and eggshell, were used for synthesis of a new magnetic activated carbon for sorption of heavy metal ions. Using response surface methodology based central composite design (RSM-CCD) technique, chicken feather and acid-digested eggshell were used as precursor and activation material, respectively, for the synthesis of the herein studied activated carbon (eggshell activated chicken feather carbon; ESCFC). The prepared activated carbon was magnetized for easy separation from water media, and iron oxide magnetized ESCFC (IOM-ESCFC) was comprehensively examined for removing some heavy metallic ions (Pb2+, Cd2+, Cu2+, Zn2+, and Ni2+) from water. The maximum mono-layer sorption capacities and the highness of sorption speed, along with thermodynamic studies, demonstrated that IOM-ESCFC can be regarded as a potential adsorbent against heavy metal ions from waters and wastewaters.

Intelligent-activated carbon prepared from pistachio shells precursor for effective adsorption of heavy metals from industrial waste of copper mine.

A novel and efficient bio-adsorbent based on magnetic activated carbon nanocomposites (MAC NCs)-modified by sulfamic acid (H3NSO3) has been developed from pistachio shell precursor as agricultural by-products and then was applied for heavy metal removal. Design an experimental model (Central Composite Design (CCD)) for adopting surface response could efficiently be used for adsorption process, and it is an economical way of obtaining the optimal adsorption conditions based on the limited number of experiments. The variants of adsorbent dosage, metal ion concentration, and contact time were optimized for Cu(II) metal by CCD. In addition, adsorption capacity and isoelectric point (pHzpc) of adsorbent were studied at different pH values. Kinetic and isotherm of adsorption were investigated via the Langmuir and the pseudo-second-order model. The maximum adsorption capacity using the Langmuir model was 277.77 mg g-1 for Cu(II) ions on H2NSO3-MAC NCs. Then adsorption process was investigated for ions of Fe(II), Zn(II), and Ni(II) under optimized condition. Also, the competitive adsorption of Fe(II), Zn(II), and Ni(II) ions mixed solution onto H2NSO3-MAC NCs was conducted. Adsorption-desorption results exhibited that the H2NSO3-MAC NCs can be used up to seven cycles while they have excellent performance. Finally, to evaluate the efficiency of this bio-adsorbent, the removal of heavy metals from wastewater of the Sarcheshmeh copper mine as a real sample was studied. Graphical abstract.