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Metal-organic frameworks (MOFs) are a class of nanoporous materials. The development of efficient and environmentally friendly methods for activating MOFs is of great significance for its industrial application. In this work, nanoscale magnetic core-shell Cu-BTC@Fe 3 O 4 was prepared through a secondary growth strategy. The effects of different activation solvents (dichloromethane and ethanol, respectively) and temperatures on the surface area, pore structures and the adsorption of xylene isomers on Cu-BTC@Fe 3 O 4 were investigated. Ethanol as an activation solvent could more easily displace the precursors remaining in the channels of Cu-BTC@Fe 3 O 4 than dichloromethane, while the temperature change has no significant influence on the pore structure. The adsorption separation of xylene isomers on Cu-BTC@Fe 3 O 4 composite materials was studied using the batch vapor-phase adsorption, and liquid-phase breakthrough experiments. The activated Cu-BTC@Fe 3 O 4 (CH 2 Cl 2 -200 ​°C ​− ​C 2 H 5 OH) material has the highest adsorption capacity of 210.26 ​mg ​g−1 for p -xylene (p X). Cu-BTC@Fe 3 O 4 (C 2 H 5 OH) and Cu-BTC@Fe 3 O 4 materials have excellent adsorption capacity for m -xylene (m X), with the values of 200.19 ​mg ​g−1 and 219.63 ​mg ​g−1, respectively, which is about 4 times higher than that of Cu-BTC@Fe 3 O 4 (CH 2 Cl 2). The adsorption capacity sequence of xylene on Cu-BTC@Fe 3 O 4 (C 2 H 5 OH) and Cu-BTC@Fe 3 O 4 materials is m -xylene (m X) ​> ​ p -xylene (p X) ​> ​ o -xylene (o X), and that of other materials is p X ​> ​ m X ​> ​ o X. Nanoscale magnetic core-shell Cu-BTC@Fe 3 O 4 was prepared through a secondary growth strategy towards the adsorption separation of xylene isomers. [Display omitted] • Nanoscale magnetic core-shell Cu-BTC@Fe 3 O 4 was prepared through a secondary growth strategy. • The effects of different activation solvents and temperatures on the xylene isomers adsorption of Cu-BTC@Fe 3 O 4 were studied. • Using ethanol as an activation solvent could more easily displace the precursors remaining in the channels of Cu-BTC@Fe 3 O 4. [ABSTRACT FROM AUTHOR]

The aim of this study was to optimize the adsorption performance of activated carbon (AC), derived from the shell of Penaeus vannamei prawns, on heavy metal ions. Inexpensive, non-toxic, and renewable prawn shells were subjected to carbonization and, subsequently, KOH-activation to produce nanoporous K-Ac. Carbonized prawn shells (CPS) and nanoporous KOH-activated carbon (K-Ac) from prawn shells were prepared and characterized by FTIR, XRD, BET, SEM, and TEM. The results showed that as-produced K-Ac samples were a porous material with microporous and mesoporous structures and had a high specific surface area of 3160 m2/g, average pore size of about 10 nm, and large pore volume of 2.38 m3/g. Furthermore, batches of K-Ac samples were employed for testing the adsorption behavior of Cd2+ in solution. The effects of pH value, initial concentration, and adsorption time on Cd2+ were systematically investigated. Kinetics and isotherm model analysis of the adsorption of Cd2+ on K-Ac showed that experimental data were not only consistent with the Langmuir adsorption isotherm, but also well-described by the quasi-first-order model. Finally, the adsorption behaviors of as-prepared K-Ac were also tested in a ternary mixture of heavy metal ions Cu2+, Cr6+, and Cd2+, and the total adsorption amount of 560 mg/g was obtained. [ABSTRACT FROM AUTHOR]

Based on the generalized gradient approximation of density functional theory, the geometric structure and electronic properties of the intrinsic Ti3C2 and Cu-, Pt-, Co-, Si-, F-, Cl- or Br-doped Ti3C2 are optimized, and the adsorption process of HCHO on the surface of the intrinsic Ti3C2 and doped Ti3C2 is calculated. The effects of adsorption energy, stability, DOS and doping on bond length were discussed. The results show that the adsorption energy of the intrinsic Ti3C2 crystal plane at the top site is the strongest, at −7.58 eV. The optimal adsorption sites of HCHO on various doping systems are Cu-Top, Pt-Top, Co-Top, Si-Hollow, Cl-Hollow, F-Bridge and Br-Hollow, respectively. Among the doped elements, anion (F, Cl, Br) doping at each adsorption site generally reduces the formaldehyde adsorption activity of the substrate; cationic doping (Cu, Pt, Co, Si) enhances the adsorption activity of the substrate for formaldehyde at most of the adsorption sites, indicating that the modification effect of anions on Ti3C2 is not as good as that of cations. The adsorption capacity of Si-doped Ti3C2 for formaldehyde was significantly improved. Compared with the intrinsic Ti3C2 crystal plane at the same adsorption site, the adsorption activity of HCHO was improved, and the highest adsorption energy was −8.09 eV. [ABSTRACT FROM AUTHOR]

Abstract: The functionalization of porous metal–organic frameworks (Cu3(BTC)2) was achieved by incorporating Keggin-type polyoxometalates (POMs), and further optimized via alkali metal ion-exchange. In addition to thermal gravimetric analysis, IR, single-crystal X-ray diffraction, and powder X-ray diffraction, the adsorption properties were characterized by N2 and volatile organic compounds (VOCs) adsorption measurements, including short-chain alcohols (C<4), cyclohexane, benzene, and toluene. The adsorption enthalpies estimated by the modified Clausius–Clapeyron equation provided insight into the impact of POMs and alkali metal cations on the adsorption of VOCs. The introduction of POMs not only improved the stability, but also brought the increase of adsorption capacity by strengthening the interaction with gas molecules. Furthermore, the exchanged alkali metal cations acted as active sites to interact with adsorbates and enhanced the adsorption of VOCs. [Copyright &y& Elsevier]

In this study, modified activated fishbone charcoal (MAFC) was successfully prepared to remove emulsified oil from oily wastewater. Various characteristic techniques, including SEM, XRD, FTIR, and BET, were employed to investigate the morphology, texture, and surface properties of as-prepared samples. BET results demonstrated that the specific surface area of fishbone charcoal increased from 69.8 m2/g to 206.0 m2/g after treatment with K2CO3 as an activating agent, while the total pore volume of MAFC increased from 0.003 cm3/g to 0.3 cm3/g, accompanied by the formation of abundant pore structures. It was observed that 90.1% of emulsified oil (100 mg/L) was successfully removed by MAFC under our experimental conditions. The results of a kinetic and isotherm model analysis indicated that the adsorption experimental data were not only consistent with the Langmuir adsorption isotherm but were also well-described by the pseudo-second-order adsorption model. It is expected that this highly efficient and inexpensive MAFC can be a promising bio-adsorbent for removing organic pollutants from industrial wastewater. [ABSTRACT FROM AUTHOR]

In this study, carbonized kelp biochar (AKB) modified by KOH impregnation and photocatalytic Bi2MoO6/AKB composite (BKBC) nanomaterials were the first time successfully synthesized for efficient removal of dyes in aqueous solution. BET, XRD, FT-IR, and SEM were employed to characterize as-prepared samples. UV-vis and other test results indicated that the removal efficiency of methylene blue (MB) was 61.39% and 94.12% for BKBC and AKB, respectively, which was up to 13 times and 20 times higher in comparison with pure Bi2MoO6 (PBM). In addition, the equilibrium adsorption capacity of MB could reach up to 324.1 mg/g for AKB. This high dyes adsorption performance could be likely attributed to its high specific surface area (507.177 m2/g) and its abundant presence of various functional groups such as –OH and =C–H on AKB. Particularly, the existing of amorphous carbon and transition metal oxides, such as Fe2O3 and Mn5O8, could be beneficial for the photodegradation of MB for AKB. Meanwhile, experimental data indicated that adsorption kinetics complied with the pseudo-second order model well, and all of the tests had satisfactory results in terms of the highly efficient adsorption and photodegradation activity of AKB nanomaterials, which suggested its great potential in wastewater treatment. [ABSTRACT FROM AUTHOR]