Thiol-functionalized magnetite/graphene oxide hybrid as a reusable adsorbent for Hg2+ removal.
Ontology highlight
ABSTRACT:
SUBMITTER: Bao J
PROVIDER: S-EPMC3842736 | biostudies-literature | 2013 Nov
REPOSITORIES: biostudies-literature
Similar Datasets
Project description:A magnetic hybrid nanomaterial, which contains magnetite (Fe3O4) particles and diazonium functionalized-reduced graphene oxide (DF-RGO), was fabricated via a three-pot reaction. First, the reduced graphene oxide (RGO) was synthesized via a redox reaction. Second, diazonium functionalized-RGO was prepared via a feasible chemical reaction. Third, Fe3O4 particles were loaded onto the surface of DF-RGO by covalent bonding, fabricating the M-DF-RGO hybrid. The fabricated hybrid was characterized by SEM, TEM, AFM, XRD, XPS, FT-IR, TGA, Raman spectroscopy, and magnetometry. The resulting M-DF-RGO hybrid possessed unique magnetic properties and was applied to remove 4-chlorophenol (4-CP) and 2,4-dichlorophenol (2,4-DCP) from aqueous solution. The adsorption of 4-CP and 2,4-DCP on the M-DF-RGO hybrid was performed under various conditions, with respect to initial chlorophenol concentration, pH, and contact time. The results suggest that the adsorption of 4-CP and 2,4-DCP onto the M-DF-RGO hybrid is strongly dependent on pH and weakly dependent on contact time. In addition, the adsorption isotherm of 4-CP and 2,4-DCP on the M-DF-RGO hybrid fits the Freundlich model well and the adsorption capacities of 4-CP and 2,4-DCP on M-DF-RGO reached 55.09 and 127.33 mg g-1, respectively, at pH 6 and 25 °C. In this situation, intermolecular interactions including π-π interactions and hydrogen bonding are operative. The calculated results of density functional theory further demonstrate that 2,4-DCP molecules could be more easily absorbed than 4-CP molecules by the M-DF-RGO hybrid. Moreover, the M-DF-RGO hybrid could be easily separated by a magnetic separation process, and showed good recyclability of more than five cycles.
| S-EPMC9078394 | biostudies-literature
Project description:In this study, EDTA functionalized corncob (EDTA-corncob) and EDTA/graphene oxide functionalized corncob (EDTA-GO/corncob) were prepared using disodium ethylenediamine tetraacetic acid and the graphene oxide immersion method. EDTA-corncob and EDTA-GO/corncob were characterized by SEM and FTIR spectroscopy. On this basis, the adsorption properties of EDTA-corncob and EDTA-GO/corncob were studied with crystal violet as the adsorbate. The optimum adsorption conditions were determined by the effect of samples on the adsorption properties of crystal violet at different times, temperatures and pH, and the reusability of the samples was studied. The results showed that adsorption capacity of crystal violet on EDTA-GO/corncob was higher compared with natural corncob and EDTA-corncob. The most suitable pH value of the solution is about 6.0, the adsorption equilibrium time is 200 min. EDTA-GO/corncob can be reused eight times. This study indicated that EDTA-GO/corncob is a reusable adsorbent for rapid, low-cost, and efficient removal of dye from waste water.
| S-EPMC9066744 | biostudies-literature
Project description:Graphene oxide (GO) holds high promise for diagnostic and therapeutic applications in nanomedicine but reportedly displays immunotoxicity, underlining the need for developing functionalized GO with improved biocompatibility. Here, we study the adverse effects of GO and amino-functionalized GO (GONH2) during Caenorhabditis elegans development and ageing upon acute or chronic exposure. Chronic GO treatment throughout the C. elegans development causes decreased fecundity and a reduction of animal size, while acute treatment does not lead to any measurable physiological decline. However, RNA-Seq data reveal that acute GO exposure induces innate immune gene expression. The p38 MAP kinase, PMK-1, which is a well-established master regulator of innate immunity, protects C. elegans from chronic GO toxicity, as pmk-1 mutants show reduced tissue-functionality and facultative vivipary. In a direct comparison, GONH2 exposure does not cause detrimental effects in the wild type or in pmk-1 mutants, and the innate immune response is considerably less pronounced. Our work establishes the enhanced biocompatibility of amino-functionalized GO in a whole-organism, emphasizing its potential as biomedical nanomaterial.
2022-05-10 | GSE131070 | GEO
Project description:Present state-of-the-art graphene-based electrodes for supercapacitors remain far from commercial requirements in terms of high energy density. The realization of high energy supercapacitor electrodes remains challenging, because graphene-based electrode materials are synthesized by the chemical modification of graphene. The modified graphene electrodes have lower electrical conductivity than ideal graphene, and limited electrochemically active surface areas due to restacking, which hinders the access of electrolyte ions, resulting in a low energy density. In order to solve the issue of restacking and low electrical conductivity, we introduce thiol-functionalized, nitrogen-doped, reduced graphene oxide scrolls as the electrode materials for an electric double-layer supercapacitor. The fabricated supercapacitor exhibits a very high energy/power density of 206 Wh/kg (59.74 Wh/L)/496 W/kg at a current density of 0.25 A/g, and a high power/energy density of 32 kW/kg (9.8 kW/L)/9.58 Wh/kg at a current density of 50 A/g; it also operates in a voltage range of 0~4 V with excellent cyclic stability of more than 20,000 cycles. By suitably combining the scroll-based electrode and electrolyte material, this study presents a strategy for electrode design for next-generation energy storage devices with high energy density without compromising the power density.
| S-EPMC6409971 | biostudies-literature
Project description:In this study, the preparation of graphene oxide@chitosan (GO@CS) composite beads was investigated via continuous dropping techniques to remove methylene blue (MB)-dye from an aqueous media. The prepared beads were characterized using various techniques before and after the adsorption of MB. The experimental results showed that the adsorption processes fit the kinetic pseudo-second-order and Langmuir isotherm models. Moreover, the GO@CS beads achieve maximum adsorption capacities of 23.26 mg g-1, which was comparable with other adsorbents in the literature. An important advantage of our adsorbent is that the GO@CS can remove 82.1% of the real sample color within 135 min.
| S-EPMC9572660 | biostudies-literature
Project description:Biochar (BC) and magnetite (Fe3O4) nanoparticles (MNP) have both received considerable recent attention in part due to their potential use in water treatment. While both are effective independently in the removal of a range of anionic metals from aqueous solution, the efficacy of these materials is reduced considerably at neutral pH due to decreased metal adsorption and MNP aggregation. In addition to synthetic metal oxide-biochar composites for use in treatment and remediation technologies, aggregates may also occur in nature when pyrolytic carbon is deposited in soils. In this study, we tested whether magnetite synthesized in the presence of biochar leads to increased removal efficiency of hexavalent chromium, Cr(VI), at the mildly acidic to neutral pH values characteristic of most natural and contaminated aqueous environments. To do so, magnetite nanoparticles and biochar produced from ground willow were synthesized to form composites (MNP-BC). Batch studies showed that MNP-BC markedly enhanced both adsorption and reduction of Cr(VI) from aqueous solution at acidic to neutral pH as compared to MNP and BC separately, suggesting a strong synergetic effect of hybridizing Fe3O4 with BC. Mechanistically, the Cr(VI) removal processes occurred through both adsorption and intraparticle diffusion followed by reduction to Cr(III). Synchrotron-based X-ray absorption spectroscopy analyses confirmed that Cr(VI) was reduced at the surface of MNP-BC, with electrons derived directly from both biochar and magnetite at low pH, while at near-neutral pH, biochar increased Cr(VI) reduction by inhibiting MNP aggregation. Extended X-ray absorption fine structure fitting results confirmed that the Cr(III) precipitates consist of Cr(OH)3 and chromite (Cr2FeO4) nanoparticles. Our results demonstrate that MNP-BC composites have great potential as a material for the treatment of chromate-containing aqueous solutions across a wide range of pH values, and provide information valuable broadly relevant to soils and sediments that contain biochar.
| S-EPMC7642354 | biostudies-literature
Project description:The pollution caused by tannery wastewater containing high concentrations of trivalent chromium ions [Cr(iii)] and organic dyes has severely restricted the sustainable development of the leather industry. To address this problem, a three-dimensional (3D) porous graphene-based hydrogel with good mechanical strength and large surface area was fabricated by self-assembly of graphene oxide (GO) sheets reduced and modified by gallic acid (GA) through π-π interactions. As an adsorbent, this GA-functionalized graphene hydrogel (GA-GH) can effectively capture Cr(iii) by coordination complexation between Cr(iii) and deprotonated carboxylic groups of GA at pH ∼ 4.0. Moreover, GA-GH could be easily regenerated by desorption of adsorbed Cr(iii) at pH 2.0 and maintained its high adsorption capacity after multiple adsorption-desorption cycles, which was also helpful for reusing desorbed Cr(iii) as tanning agent. In addition, compared with a graphene hydrogel (GH) without modification by GA, adsorption capacity of GA-GH for organic dye was significantly improved due to the enhanced π-π interactions between the GA-GH and aromatic dyes.
| S-EPMC9070501 | biostudies-literature
Project description:A hybrid material obtained by blending ?-chitosan (CS) with triethylenetetramine-functionalized graphene oxide (TFGO) (CSGO), was used as an adsorbent for a reactive dye (C.I. Reactive Blue 221 Dye, RB221), and the adsorption and removal performances of unmodified CS and mix-modified CSGO were investigated and compared systematically at different pH values (2, 3, 4, 5, 6, 7, 8, 9, 10, 11, and 12). The adsorption capacities of CS and CSGO were 45.5 and 56.1 mg/g, respectively, at a pH of 2 and 5.4 and 37.2 mg/g, respectively, at a pH of 12. This indicates that TFGO was successfully introduced into CSGO, enabling ?-? interactions and electrostatic attraction with the dye molecules. Additionally, benzene ring-shaped GO exhibited a high surface chemical stability, which was conducive to maintaining the stability of the acid and alkali resistance of the CSGO adsorbent. The RB221 adsorption performance of CS and CSGO at acidic condition (pH 3) and alkaline condition (pH 12) and different temperatures was investigated by calculating the adsorption kinetics and isotherms of adsorbents. Overall, the adsorption efficiency of CSGO was superior to that of CS; thus, CSGO is promising for the treatment of dye effluents in a wide pH range.
| S-EPMC7221750 | biostudies-literature
Project description:This work demonstrates very high removal rates (below the detection limit of 0.045 ppb) of inorganic arsenic from water using electrospun polyvinylidene difluoride (PVDF) membranes enhanced by the addition of functionalized graphene oxide in membrane distillation. This shows potential for applications in the many parts of the world suffering from arsenic-contaminated groundwater. These membranes were enhanced by the addition of reduced graphene oxide functionalized with superhydrophobic polyhedral oligomeric silsesquioxane molecules (POSS-rGO) into the spinning solutions. The flux of the best-performing rGO-enhanced membrane (containing 2 wt % POSS-rGO) was 21.5% higher than that of the pure PVDF membrane and almost double that of a commercial polytetrafluoroethylene (PTFE) membrane after 24 h of testing, with rejection values exceeding 99.9%. Furthermore, the flux of this membrane was stable over 5 days (∼28 L m-2 h-1) of continuous testing and was more stable than those of the PTFE and control membranes when treating a concentrated fouling solution of calcium carbonate and iron(III) sulfate heptahydrate. It also achieved higher permeate quality in these conditions. The Young's modulus and ultimate tensile strength of the best-performing membrane increased by 38 and 271%, respectively, compared to the pure polymer membrane, while both had similar porosities of ∼91%.
| S-EPMC8154216 | biostudies-literature
Project description:High-density polyethylene (HDPE)-based and ultra-high molecular weight polyethylene (UHMWPE)-based composites with carbonaceous reinforcements are being widely investigated for biomedical applications. The enhancement of material properties critically depends on the nature, amount and compatibility of the reinforcement with the polymeric matrix. To this end, this study demonstrates the efficacy of a 'dual' hybrid approach of incorporating modified inorganic nanofiller into an optimized polyethylene blend. In particular, a unique synthesis strategy was adopted to design a covalently bonded maleated polyethylene (mPE) grafted modified graphene oxide (mGO) hybrid nanocomposite. In this scheme, polyethyleneimine (PEI) was initially attached onto GO to synthesize amine functionalized GO (GO-PEI). This is followed by mPE grafting, resulting in mGO. Melt-extrusion together with injection moulding of a polymer mix (60% HDPE-40% UHMWPE) with different proportions (less than or equal to 3 wt%) of surface functionalized GO was conducted to develop nanocomposites of different sizes and shapes. When compared with unreinforced PE blend, the nanocomposites with 1 wt% mGO exhibited an increase in ultimate tensile strength by 120% (up to 65 MPa) and elastic modulus by 40% (up to 908 MPa). The uniform dispersion of modified GO nanofillers, confirmed using X-ray micro-computed tomography and transmission electron microscopy, facilitated effective interfacial adhesion and compatibility with the hybrid polymer matrix. The variation in mechanical properties with GO/mGO addition to PE blend was critically discussed in reference to the structural modification of GO, crystallinity and nature of dispersion of fillers. Importantly, the nanocomposites support the attachment and proliferation of C2C12 murine myoblast cells over 3 days in culture in a statistically insignificant manner with respect to polymer blends without any nanofiller. Taken together, the experimental results suggest that HDPE/UHMWPE/mGO is a promising biomaterial for bone tissue engineering applications.
| S-EPMC6364642 | biostudies-literature