Browse
Submit Data
Databases
API
Help

Dataset Information

16 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

A facile synthesis of porous graphene for efficient water and wastewater treatment.

ABSTRACT: The use of two-dimensional graphene-based materials in water treatment has recently gained significant attention due to their unique electronic and thermal mobility, high surface area, high mechanical strength, excellent corrosion resistance and tunable surface chemistry. However, the relatively expensive, poor hydrophobicity, low adsorption capacity and recyclability, and complex post-treatment of the most pristine graphene frameworks limit their practical application. Here, we report a facile scalable method to produce highly porous graphene from reduced graphene oxide via thermal treatment without addition of any catalyst or use of any template. Comparing to conventional graphene counterparts, as-prepared porous graphene nanosheets showed evident improvement in hydrophobicity, adsorption capacity, and recyclability, making them ideal candidate materials for water treatment. Superhydrophobic and superoleophilic porous graphene prepared in this work has been demonstrated as effective absorbents for a broad range of ions, oils and organic solvents, exhibiting high selectivity, good recyclability, and excellent absorption capacities > 90%. The synthesis method of porous graphene reported in this paper is easy to implement, low cost and scalable. These attributes could contribute towards efficient and cost-effective water purification and pollution reduction.

SUBMITTER: Tabish TA

PROVIDER: S-EPMC5788977 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

Facile synthesis of reduced graphene oxide-gold nanohybrid for potential use in industrial waste-water treatment.

Project description:Here, we report a facile approach, by the photochemical reduction technique, for in situ synthesis of Au-reduced graphene oxide (Au-RGO) nanohybrids, which demonstrate excellent adsorption capacities and recyclability for a broad range of dyes. High-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) data confirm the successful synthesis of Au-RGO nanohybrids. The effect of several experimental parameters (temperature and pH) variation can effectively control the dye adsorption capability. Furthermore, kinetic adsorption data reveal that the adsorption process follows a pseudo second-order model. The negative value of Gibbs free energy (ΔG0) confirms spontaneity while the positive enthalpy (ΔH0) indicates the endothermic nature of the adsorption process. Picosecond resolved fluorescence technique unravels the excited state dynamical processes of dye molecules adsorbed on the Au-RGO surface. Time resolved fluorescence quenching of Rh123 after adsorption on Au-RGO nanohybrids indicates efficient energy transfer from Rh123 to Au nanoparticles. A prototype device has been fabricated using Au-RGO nanohybrids on a syringe filter (pore size: 0.220 μm) and the experimental data indicate efficient removal of dyes from waste water with high recyclability. The application of this nanohybrid may lead to the development of an efficient reusable adsorbent in portable water purification.

| S-EPMC5101912 | biostudies-literature

Facile Synthesis of Porous Carbon for the Removal of Diclofenac Sodium from Water.

Project description:In this work, a series of porous carbon materials (PCs) were obtained at different carbonization temperatures (800, 900, 1000, and 1100 °C) by a simple and fast solvent-free method. Moreover, the feasibility of PCs as reliable and efficient adsorbents to capture diclofenac sodium (DCF) from the water was evaluated. Notably, porous carbon (PC) prepared at 1000 °C (PC-1000) was found to be the best candidate for the adsorption of DCF. Remarkably, adsorption equilibrium was achieved within 3 h, which followed a pseudo-second-order kinetic model with a high correlation coefficient (R 2 > 0.994). Furthermore, experimental data obtained from adsorption isotherm indicated that the capture of DCF onto PC-1000 followed the Langmuir adsorption model (R 2 > 0.997), wherein its maximum adsorption capacity was calculated to be 392 mg/g. In addition, based on the results obtained from the zeta potential of PC-1000 under different pH and the adsorbed quantity of DCF along with functional groups created on the surface of PC-1000, electrostatic and H-bonding interactions were proposed as the possible adsorption mechanisms. Due to its high stability and excellent reusability, PC-1000 has been testified as a promising candidate for removing DCF from contaminated water.

| S-EPMC6751710 | biostudies-literature

Facile electrodeposition of V-doped CoP on vertical graphene for efficient alkaline water electrolysis.

Project description:In this work, we demonstrate a highly enhanced electrocatalytic activity of vanadium-doped CoP (V-CoP), directly grafted on a vertical graphene/carbon cloth electrode (VG/CC) by a facile electrochemical deposition method. Impressively, V-CoP/VG/CC exhibited a superior catalytic activity toward the hydrogen evolution reaction (HER) in alkaline solution. Compared to CoP/VG/CC, V-doping decreased the overpotential for HER at 10 mA cm-2 by more than half to 40 mV. The new catalyst even outperformed Pt/C beyond 150 mA cm-2. The overpotential for OER at 50 mA cm-2 was merely 314 mV, more than 100 mV lower than that of IrO2. Moreover, our novel catalyst worked as an excellent bifunctional catalyst with a low cell voltage of 1.69 V to achieve a current density of 50 mA cm-2. Detailed characterizations revealed that the V-doping in CoP resulted in improved electrical conductivity and increased active sites. Our findings highlight the significant advantage of V doping on the catalytic activities of CoP, already boosted by VG. Furthermore, concurrent doping with the electrodeposition of catalyst offers a new approach for practical water electrolysis.

| S-EPMC9051416 | biostudies-literature

A Facile Synthesis of Nitrogen-Doped Highly Porous Carbon Nanoplatelets: Efficient Catalysts for Oxygen Electroreduction.

Project description:The oxygen reduction reaction (ORR) is of great importance for various renewable energy conversion technologies such as fuel cells and metal-air batteries. Heteroatom-doped carbon nanomaterials have proven to be robust metal-free electrocatalysts for ORR in the above-mentioned energy devices. Herein, we demonstrate the synthesis of novel highly porous N-doped carbon nanoplatelets (N-HPCNPs) derived from oatmeal (or a biological material) and we show the materials' high-efficiency as electrocatalyst for ORR. The obtained N-HPCNPs hybrid materials exhibit superior electrocatalytic activities towards ORR, besides excellent stability and good methanol tolerance in both basic and acidic electrolytes. The unique nanoarchitectures with rich micropores and mesopores, as well as the high surface area-to-volume ratios, present in the materials significantly increase the density of accessible catalytically active sites in them and facilitate the transport of electrons and electrolyte within the materials. Consequently, the N-HPCNPs catalysts hold a great potential to serve as low-cost and highly efficient cathode materials in direct methanol fuel cells (DMFCs).

| S-EPMC5327468 | biostudies-literature

Facile synthesis of crystalline viologen-based porous ionic polymers with hydrogen-bonded water for efficient catalytic CO<sub>2</sub> fixation under ambient conditions.

Project description:In this work, we report a series of crystalline viologen-based porous ionic polymers (denoted VIP-X, X = Cl or Br), that have in situ formed dicationic viologens paired with halogen anions and intrinsic hydrogen-bonded water molecules, towards metal-free heterogeneous catalytic conversion of carbon dioxide (CO2) under mild conditions. The targeted VIP-X materials were facilely constructed via the Menshutkin reaction of 4,4'-bipyridine with 4,4'-bis(bromomethyl)biphenyl (BCBMP) or 4,4'-bis(chloromethyl)biphenyl (BBMBP) monomers. Their crystalline and porous structures, morphological features and chemical structures and compositions were fully characterized by various advanced techniques. The optimal catalyst VIP-Br afforded a high yield of 99% in the synthesis of cyclic carbonate by CO2 cycloaddition with epichlorohydrin under atmospheric pressure (1 bar) and a low temperature (40 °C), while other various epoxides could be also converted into cyclic carbonates under mild conditions. Moreover, the catalyst VIP-Br could be separated easily and reused with good stability. The remarkable catalytic performance could be attributed to the synergistic effect of the enriched Br- anions and available hydrogen bond donors -OH groups coming from H-bonded water molecules.

| S-EPMC9048747 | biostudies-literature

Facile Synthesis of Vertically Arranged CNTs for Efficient Solar-Driven Interfacial Water Evaporation.

Project description:Solar-driven evaporation of water is a sustainable and promising technology for addressing the crisis of clean water. Herein, novel vertically arranged carbon nanotube (V-CNT) aerogels with a tree branch structure is facilely synthesized through an ice templating method. The V-CNT-based photothermal evaporator exhibits efficient broadband light trapping and super-hydrophilicity. Owing to the unique structure and ultrafast water transportation, a high evaporation rate of 3.26 kg m-2 h-1 was achieved by the three-dimensional V-CNT-based evaporator under a solar illumination of 1 kW m-2. More significantly, the V-CNT shows excellent recycling stability and salt-resistant performance in seawater and may provide a novel strategy to the practical sustainable technique of water purification applications.

| S-EPMC9774377 | biostudies-literature

Facile Synthesis of BiVO4@ZIF-8 Composite with Heterojunction Structure for Photocatalytic Wastewater Treatment.

Project description:Water pollution has always been a serious problem across the world; therefore, facile pollutant degradation via light irradiation has been an attractive issue in the field of environmental protection. In this study, a type of Zn-based metal-organic framework (ZIF-8)-wrapped BiVO4 nanorod (BiVO4@ZIF-8) with high efficiency for photocatalytic wastewater treatment was synthesized through a two-step hydrothermal method. The heterojunction structure of BiVO4@ZIF-8 was confirmed by morphology characterization. Due to the introduction of mesoporous ZIF-8, the specific surface area reached up to 304.5 m2/g, which was hundreds of times larger than that of pure BiVO4 nanorods. Furthermore, the band gap of BiVO4@ZIF-8 was narrowed down to 2.35 eV, which enabled its more efficient utilization of visible light. After irradiation under visible light for about 40 min, about 80% of rhodamine B (RhB) was degraded, which was much faster than using pure BiVO4 or other BiVO4-based photocatalysts. The synergistic photocatalysis mechanism of BiVO4@ZIF-8 is also discussed. This study might offer new pathways for effective degradation of wastewater through facile design of novel photocatalysts.

| S-EPMC8658979 | biostudies-literature

Performance Evaluation of Porous Graphene as Filter Media for the Removal of Pharmaceutical/Emerging Contaminants from Water and Wastewater.

Project description:Graphene and its counterparts have been widely used for the removal of contaminants from (waste)water but with limited success for the removal of pharmaceutical contaminants. Driven by this need, this study reports, for the first time, the removal of pharmaceuticals from real contaminated water samples using porous graphene (PG) as a filter-based column. This work systematically evaluates the performance of PG as a filter medium for the removal of widely consumed pharmaceutical/emerging contaminants (ECs) such as atenolol, carbamazepine, ciprofloxacin, diclofenac, gemfibrozil and ibuprofen. Several factors were investigated in these column studies, including different reactive layer configurations, bed packing heights (5-45 mm), filter sizes (inner diameter 18-40 mm), adsorbent dosages (100-500 mg-PG) and water bodies (distilled water, greywater, and actual effluent wastewater). Sustainable synthesis of PG was carried out followed by its use as a filter medium for the removal of pharmaceuticals at high concentrations (10.5 ± 0.5 mg/L) and trace concentrations (1 mg/L). These findings revealed that the double-layered PG-sand column outperformed a PG single-layered configuration for the removal of most of the ECs. The removal efficiency of ECs from their solutions was improved by increasing PG dosages and filter bed height and size. Although the treatment of mixed pharmaceutical solutions from different water bodies was affected by the negative interference caused by competing water compounds, the treatment of ECs-contaminated greywater was not severely affected. Our findings suggest that PG, as a highly efficient filter medium, could be used for the removal of emerging pharmaceutical contaminants from water and wastewater.

| S-EPMC7824533 | biostudies-literature

Facile Synthesis of Magnetic Nitrogen-Doped Porous Carbon from Bimetallic Metal?Organic Frameworks for Efficient Norfloxacin Removal.

Project description:Magnetic nitrogen-doped porous carbon (MNPC) has been prepared via self-catalytic pyrolysis of bimetallic metal-organic frameworks (MOFs). The as-obtained MNPC showed favorable features for antibiotics adsorption such as high specific surface area (871 m² g-1), high pore volume (0.75 cm³ g-1), porous structure, good graphitization degree, and rich N-doping. Moreover, the MNPC has magnetic properties due to the Co species, which is embedded with a high dispersion, so the absorbent can be easily separated. Based on the above excellent characteristics, the MNPC was used as the absorbent for norfloxacin (NOR) removal. The experimental maximum NOR adsorption capacity of MNPC was 55.12 mg g-1 at 298.15 K and a pH of 6.0 with an initial NOR concentration of 50 mg L-1. The data analysis of the kinetics revealed that the experimental data of NOR uptakes versus time agreed with the pseudo-second order model. The isotherm data analysis revealed the favorable application of the Freundlich model. Based on the adsorption results over a wide range of conditions, the dominant adsorption mechanisms were found to be pore-filling, electrostatic interaction, and the H-bond.

| S-EPMC6165088 | biostudies-other

Water-enhanced Removal of Ciprofloxacin from Water by Porous Graphene Hydrogel.

Project description:An environmentally benign and efficient hydrothermal reduction method was applied for the preparation of three-dimensional (3D) porous graphene hydrogel (GH) adsorbents. The physicochemical properties of GH granules were systematically characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), Raman spectra and Brunauer-Emmett-Teller (BET) method. GH granules showed an excellent adsorption capacity (235.6 mg/g) for ciprofloxacin via combined adsorption interaction mechanisms (e.g. π-π EDA interaction, hydrogen bonding, and hydrophobic interaction). Moreover, reducing the size of the hydrogels can significantly accelerate the adsorption process and enhance the removal efficiency of pollutants from aqueous solution. Water (more than 99 wt%) within hydrogels played a key role in enhancing adsorption performance. The GO hydrogels exhibited an excellent adaptability to environmental factors. These findings demonstrate that GH granules are promising adsorbents for the removal of antibiotic pollutants from aqueous solutions.

| S-EPMC4559748 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data