Activated boron nitride as an effective adsorbent for metal ions and organic pollutants.
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ABSTRACT:
SUBMITTER: Li J
PROVIDER: S-EPMC3826095 | biostudies-literature |
REPOSITORIES: biostudies-literature
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Project description:Elegant integration of three-dimensional (3D) boron nitride (BN) into the porous structure of a polymer nanofiber (NF) membrane system results in a surface with enhanced absorption capacity for removal. Various BN-based applications were designed and developed successfully, but BN-based absorption systems remain relatively unexplored. To develop a reusable absorption strategy with high removal efficiency, we used a composite of 3D BN and polyacrylonitrile (PAN) to prepare a NF membrane with a porous structure by using electrospinning and spray techniques (BN-PAN ES NFs). The removal efficiency of the 3D BN NF membrane was higher than that of a pure carbon NF membrane. Water pollutants, such as the dyes Congo red (CR), basic yellow 1 (BY), and rhodamine B (Rh B), were tested, and the absorption ratios were 46%, 53%, and 45%, respectively. Furthermore, the aforementioned dyes and pollutants can be completely eliminated and removed from water by heating because of the high heat resistance of 3D BN. The membrane can be recycled and reused at least 10 times. These results indicate that BN-PAN ES NFs have can be used in water purification and treatment for absorption applications, and that they can be reused after heat treatment.
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Project description:Two-dimensional layered materials doped with transition metals exhibit enhanced magnetization and improved catalytic stability during water treatment leading to potential environmental applications across several industrial sectors. In the present study, cobalt (Co)-doped boron nitride nanosheets (BN-NS) were explored for such an application. Chemical exfoliation process was used to exfoliate BN-NS and the hydrothermal route was adopted to incorporate Co dopant in various concentrations (e.g., 2.5, 5, 7.5, and 10?wt%). X-ray diffraction (XRD) study indicated that crystallinity improved upon doping with the formation of a hexagonal phase of the synthesized material. Selected area electron diffraction (SAED) confirmed enhanced crystallinity, which corroborates XRD results. Interlayer spacing was evaluated through a high-resolution transmission electron microscope (HR-TEM) equipped with Gatan digital micrograph software. Compositional and functional group analysis was undertaken with energy dispersive X-ray (EDS) and Fourier transform infrared (FTIR) spectroscopy, respectively. Field emission scanning electron microscope (FE-SEM) and HR-TEM were utilized to probe surface morphologies of prepared samples. Bonding modes in the sample were identified through Raman analysis. Optical properties were examined using UV-vis spectroscopy. Photoluminescence spectra were acquired to estimate the separation and recombination of excitons. Magnetic properties were studied by means of hysteresis loop acquired using VSM measurements. Methylene blue dye was degraded with as-prepared host and doped nanosheets used as catalysts and investigated through absorption spectra ranging from 250 to 800?nm. The experimental results of this study indicate that Co-doped BN-NS showed enhanced magnetic properties and can be used to degrade dyes present as an effluent in industrial wastewater.
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Project description:Catalytic hydrogenation is an important process used for the production of everything from foods to fuels. Current heterogeneous implementations of this process utilize metals as the active species. Until recently, catalytic heterogeneous hydrogenation over a metal-free solid was unknown; implementation of such a system would eliminate the health, environmental, and economic concerns associated with metal-based catalysts. Here, we report good hydrogenation rates and yields for a metal-free heterogeneous hydrogenation catalyst as well as its unique hydrogenation mechanism. Catalytic hydrogenation of olefins was achieved over defect-laden h-BN (dh-BN) in a reactor designed to maximize the defects in h-BN sheets. Good yields (>90%) and turnover frequencies (6 × 10-5-4 × 10-3) were obtained for the hydrogenation of propene, cyclohexene, 1,1-diphenylethene, (E)- and (Z)-1,2-diphenylethene, octadecene, and benzylideneacetophenone. Temperature-programmed desorption of ethene over processed h-BN indicates the formation of a highly defective structure. Solid-state NMR (SSNMR) measurements of dh-BN with high and low propene surface coverages show four different binding modes. The introduction of defects into h-BN creates regions of electronic deficiency and excess. Density functional theory calculations show that both the alkene and hydrogen-bond order are reduced over four specific defects: boron substitution for nitrogen (BN), vacancies (VB and VN), and Stone-Wales defects. SSNMR and binding-energy calculations show that VN are most likely the catalytically active sites. This work shows that catalytic sites can be introduced into a material previously thought to be catalytically inactive through the production of defects.
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Project description:In this paper, biochar derived from poplar catkins was used as an economical and renewable adsorbent for adsorption organic and inorganic pollutants such as, dyes, organic compounds, and heavy metal ions from wastewater. Mesoporous activated carbonized poplar catkins (ACPCs) were produced from char as a by-product by carbonized poplar catkins (CPCs). With their high surface area, ACPCs exhibited the maximum adsorption capacities of 71.85 and 110.17 mg/g for the removal of inorganic U(VI) and Co(II). Compared other biochars adsorbents, ACPCs can also adsorb organic pollutants with the maximum adsorption capacities of 534, 154, 350, 148 and 384 mg/g for methylene blue (MB), methyl orange (MO), Congo red (CR), chloramphenicol (CAP) and naphthalene. The adsorption of organic pollutants was fitted with pseudo-first order, pseudo-second order, and intra-particle diffusion kinetic models figure out the kinetic parameters and adsorption mechanisms. Langmuir adsorption isotherm was found to be suitable for Co(II) and U(VI) adsorption and thermodynamic studies indicated adsorption processes to be endothermic and spontaneous. The adsorption process includes both outer-sphere surface complexes and hydrogen-bonding interactions. The results showed that biochar derived from poplar catkins was a potential material to remove pollutants in wastewater.
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Project description:Metal-semiconductor-metal (MSM) detectors based on Ti/Au and Ni/Au interdigitated structures were fabricated using 2.5 micrometer thick hexagonal boron nitride (h-BN) layer with both natural and 10B-enriched boron. Current-voltage (I-V) and current-time (I-t) curves of the fabricated detectors were recorded with (I N) and without (I d) neutron irradiation, allowing the determination of their sensitivity (S = (I N - I d)/I d = ΔI/I d). Natural and 10B-enriched h-BN detectors exhibited high neutron sensitivities of 233 and 367% at 0 V bias under a flux of 3 × 104 n/cm2/s, respectively. An imbalance in the distribution of filled traps between the two electric contacts could explain the self-biased operation of the MSM detectors. Neutron sensitivity is further enhanced with electrical biasing, reaching 316 and 1192% at 200 V and a flux of 3 × 104 n/cm2/s for natural and 10B-enriched h-BN detectors, respectively, with dark current as low as 2.5 pA at 200 V. The increased performance under bias has been attributed to a gain mechanism based on neutron-induced charge carrier trapping at the semiconductor/metal interface. The response of the MSM detectors under thermal neutron flux and bias voltages was linear. These results clearly indicate that the thin-film monocrystal BN MSM neutron detectors can be optimized to operate sensitively with the absence of external bias and generate stronger signal detection using 10B-enriched boron.
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Project description:Liquids confined down to the atomic scale can show radically new properties. However, only indirect and ensemble measurements operate in such extreme confinement, calling for novel optical approaches that enable direct imaging at the molecular level. Here we harness fluorescence originating from single-photon emitters at the surface of hexagonal boron nitride for molecular imaging and sensing in nanometrically confined liquids. The emission originates from the chemisorption of organic solvent molecules onto native surface defects, revealing single-molecule dynamics at the interface through the spatially correlated activation of neighbouring defects. Emitter spectra further offer a direct readout of the local dielectric properties, unveiling increasing dielectric order under nanometre-scale confinement. Liquid-activated native hexagonal boron nitride defects bridge the gap between solid-state nanophotonics and nanofluidics, opening new avenues for nanoscale sensing and optofluidics.
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Project description:We demonstrate wafer-scale growth of high-quality hexagonal boron nitride (h-BN) film on Ni(111) template using metal-organic chemical vapor deposition (MOCVD). Compared with inert sapphire substrate, the catalytic Ni(111) template facilitates a fast growth of high-quality h-BN film at the relatively low temperature of 1000 °C. Wafer-scale growth of a high-quality h-BN film with Raman E2g peak full width at half maximum (FWHM) of 18~24 cm-1 is achieved, which is to the extent of our knowledge the best reported for MOCVD. Systematic investigation of the microstructural and chemical characteristics of the MOCVD-grown h-BN films reveals a substantial difference in catalytic capability between the Ni(111) and sapphire surfaces that enables the selective-area growth of h-BN at pre-defined locations over a whole 2-inch wafer. These achievement and findings have advanced our understanding of the growth mechanism of h-BN by MOCVD and will contribute an important step toward scalable and controllable production of high-quality h-BN films for practical integrated two-dimensional materials-based systems and devices.
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Project description:We have developed a simple one-step method to synthesize novel supramolecular polysaccharide composites from cellulose (CEL), chitosan (CS) and benzo-15-crown 5 (B15C5). Butylmethylimidazolium chloride [BMIm(+)Cl(-)], an ionic liquid (IL), was used as a sole solvent for dissolution and preparation of the composites. Since majority of [BMIm(+)Cl(-)] used was recovered for reuse, the method is recyclable. The [CEL/CS+B15C5] composites obtained retain properties of their components, namely superior mechanical strength (from CEL), excellent adsorption capability for heavy metal ions and organic pollutants (from B15C5 and CS). More importantly, the [CEL/CS+B15C5] composites exhibit truly supramolecular properties. By itself CS, CEL and B15C5 can effectively adsorb Cd(2+), Zn(2+) and 2,4,5-trichlorophenol. However, adsorption capability of the composite was substantially and synergistically enhanced by adding B15C5 to either CEL and/or CS. That is, the adsorption capacity (qe values) for Cd(2+) and Zn(2+) by [CS+B15C5], [CEL+B15C5] and [CEL+CS+B15C5] composites are much higher than combined qe values of individual CS, CEL and B15C5 composites. It seems that B15C5 synergistically interact with CS (or CEL) to form more stable complexes with Cd(2+) (or Zn(2+)), and as a consequence, the [CS+B15C5] (or the [CEL+B15C5]) composite can adsorb relatively larger amount Cd(2+) (or Zn(2+)). Moreover, the pollutants adsorbed on the composites can be quantitatively desorbed to enable the [CS+CEL+B15C5] composites to be reused with similar adsorption efficiency.
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Project description:This paper reports the successful synthesis of magnetic nanocomposite of calcium ferrite with nitrogen doped graphene oxide (CaFe2O4-NGO) for the effective removal of Pb(II) ions and photocatalytic degradation of congo red and p-nitrophenol. X-ray diffraction (XRD), Fourier transform infrared (FT-IR), transmission electron microscopy (TEM), and scanning electron microscopy-energy dispersive X-ray (SEM-EDX) techniques confirmed the presence of NGO and CaFe2O4 in the nanocomposite. The Mössbauer studies depicted the presence of paramagnetic doublet and sextet due to presence of CaFe2O4 NPs in the nanocomposite. The higher BET surface area in case of CaFe2O4-NGO (52.86 m2/g) as compared to CaFe2O4 NPs (23.45 m2/g) was ascribed to the effective modulation of surface in the presence of NGO. Adsorption followed the Langmuir model with maximum adsorption capacity of 780.5 mg/g for Pb(II) ions. Photoluminescence spectrum of nanocomposite displayed four-fold decrease in the intensity, as compared to ferrite NPs, thus confirming its high light capturing potential and enhanced photocatalytic activity. The presence of NGO in nanocomposite offered an excellent visible light driven photocatalytic performance. The quenching experiments supported ●OH and O2●- radicals as the main reactive species involved in carrying out the catalytic system. The presence of Pb(II) had synergistic effect on photocatalytic degradation of pollutants. This study highlights the synthesis of CaFe2O4-NGO nanocomposite as an efficient adsorbent and photocatalyst for remediating pollutants.
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Project description:Over the past decades, desalination by reverse osmosis (RO) membranes has attracted increasing attention. Although RO has proven its efficiency, it remains, however, relatively costly because of the use of high-pressure pumps and the low water permeability of conventional cross-linked polymer membranes. One route to improve the desalination performance consists of using membranes made from sub-nanoporous boron nitride (sNBN) monolayers. Indeed, by using molecular dynamics simulations, we report here that the water permeability of such sNBN membranes far exceeds that of conventional RO polymer membranes and is even higher than that of nanoporous graphene while the ion rejection remains close to 100%. At the same time, the molecular mechanism of water and ion transport through sNBN has been elucidated, with special attention paid to the impact of ions on water permeability through sNBN membranes.
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