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Toward Large-Scale Production of Oxidized Graphene.

ABSTRACT: The oxidative exfoliation of graphite is a promising approach to the large-scale production of graphene. Conventional oxidation of graphite essentially facilitates the exfoliation process; however, the oxidation procedure releases toxic gases and requires extensive, time-consuming steps of washing and reduction to convert exfoliated graphene oxide (GO) into reduced graphene oxide (rGO). Although toxic gases can be controlled by modifying chemical reactions, filtration, dialysis, and extensive sonication are unfavorable for large-scale production. Here, we report a complete, scalable, and green synthesis of GO, without NaNO3, followed by reduction with citric acid (CA). This approach eliminates the generation of toxic gases, simplifies the washing steps, and reduces the time required to prepare rGO. To validate the proposed method, we present spectroscopical and morphological studies, using energy-dispersive X-ray spectroscopy (EDS), UV-visible spectroscopy, infrared spectroscopy, Raman spectroscopy, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Thermal gravimetric analysis (TGA) is used to analyze the thermal properties of GO and rGO. This eco-friendly method proposes a complete guideline protocol toward large-scale production of oxidized graphene, with potential applications in supercapacitors, fuel cells, composites, batteries, and biosensors.

SUBMITTER: Tene T

PROVIDER: S-EPMC7075232 | biostudies-literature | 2020 Feb

REPOSITORIES: biostudies-literature

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Toward Large-Scale Production of Oxidized Graphene.

Tene Talia T Tubon Usca Gabriela G Guevara Marco M Molina Raul R Veltri Francesco F Arias Melvin M Caputi Lorenzo S LS Vacacela Gomez Cristian C

Nanomaterials (Basel, Switzerland) 20200206 2

The oxidative exfoliation of graphite is a promising approach to the large-scale production of graphene. Conventional oxidation of graphite essentially facilitates the exfoliation process; however, the oxidation procedure releases toxic gases and requires extensive, time-consuming steps of washing and reduction to convert exfoliated graphene oxide (GO) into reduced graphene oxide (rGO). Although toxic gases can be controlled by modifying chemical reactions, filtration, dialysis, and extensive so ...[more]

PMID: 32041339

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Project description:Graphene has unprecedented physical, chemical, and electronic properties, but need of the hour is to develop low-dimensional nanomaterials, such as graphene quantum dots (GQDs), that could be incorporated into nanoscale devices. This article depicts the production of GQDs from ultrafine, thin (0.8-1 nm), bilayer graphene sheets (GSs) possessing large micron-sized lateral dimension, low defect density (I D/I G: 0.1), and oxidation degree (C/O ratio: 27) of lowest level, in contrast to many other techniques where synthesis of GSs was done using analytical-grade expensive graphite electrodes. This low-cost manufacturing of GSs for industrial-scale applications was achieved by utilizing only 99%-purity graphite electrodes. The variants of such graphite electrodes (graphite rod, film, pencil) are etched in different pH electrolytes (H2SO4, NaCl, NaOH) via prompt electrochemical exfoliation, each giving more than 50% yield. Nowadays, semiconductor quantum dots (QDs) are utilized in smart device production industries, but their toxicity is a major issue of concern. Therefore, the dimension of this two-dimensional (2D) material is reduced to <10 nm to generate GQDs. A facile and highly reproducible approach has been reported for the large-scale generation of GQDs (size ca. 6-10 nm) with minimal surface defects. The protocol followed in this article to synthesize GQDs involves the use of ethylenediamine (en), which passivates the surface and reduces defects, thereby enhancing the optical properties. We demonstrate the correlation of the electrochemical and hydrothermal parameters with the growth mechanism and morphological, structural, chemical, and optical properties of the graphene nanomaterials. Raman spectroscopy and X-ray diffraction (XRD) reveal the structural configurations of GSs and GQDs to investigate the nature of defects. Field emission scanning electron microscopy (FESEM) confirms the morphological characteristics of the as-prepared GSs and GQDs with energy-dispersive X-ray (EDX) analysis determining the C/O ratio. The optical properties like UV-visible absorption and fluorescence assays show the quantum confinement effect phenomenon in GQDs. The obtained GSs and GQDs display enhanced solution stability in DI water and other solvents due to controllable oxidation degree as elucidated through Fourier transform infrared (FTIR) analysis.

Project description:Hematopoietic stem and progenitor cells (HSPCs) have been cultured using a wide variety of cytokines to promote differentiation into megakaryocytic cells (Mks), the precursors to platelets. Greater Mk DNA content, or ploidy, has been correlated with increased platelet release. Gradients of pH, pO2, and signaling factors regulate megakaryopoiesis in the bone marrow niche. In this study, we demonstrate that a 3-phase culture process with increasing pH and pO2 and different cytokine cocktails greatly increases megakaryocyte production. CD34(+) HSPCs were first cultured at 5% O2 and pH 7.2 with a cytokine cocktail previously shown to promote Mk progenitor production. At day 5, cells were shifted to 20% O2 and pH 7.4 and maintained in 1 of 17 cytokine cocktails identified using a 2(4) factorial design of experiments method to evaluate the effects of interleukin (IL)-3, IL-6, IL-9, and high- or low-dose stem cell factor (SCF), in conjunction with thrombopoietin (Tpo) and IL-11, on expansion of mature Mks from progenitors. The combination of Tpo, high-dose SCF, IL-3, IL-9, and IL-11 best promoted Mk expansion. IL-3 greatly increased total cell fold expansion, but this was partially offset by lower Mk purity. IL-9 promoted CD41 and CD42b expression. High-dose (100?ng/mL) SCF increased Mk production and ploidy. Different commercial media and IL-3 sources substantially impacted differentiation, and X-VIVO 10 serum-free media best supported mature Mk expansion. Shifting from pH 7.4 to pH 7.6 at day 7 increased Mk production by 30%. Treatment with nicotinamide at day 7 or day 8 more than doubled the fraction of high-ploidy (>4N) Mks. Ultimately, the 3-phase culture system gave rise to 44.5±8.1?Mks and 8.5±3.1 high-ploidy Mks per input HSPC. Further optimization was required to improve platelet production. Using Iscove's modified Dulbecco's medium (IMDM)+20% BSA, insulin and transferin (BIT) 9500 Serum Substitute greatly improved the frequency and quality of Mk proplatelet extensions without affecting Mk expansion, commitment, or polyploidization in the 3-phase process. Mks cultured in IMDM+20% BIT 9500 gave rise to platelets with functional activity similar to that of fresh platelets from normal donors, as evidenced by basal tubulin distribution and the expression of surface markers and spreading in response to platelet agonists.

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Toward Large-Scale Production of Oxidized Graphene.

Publications

Toward Large-Scale Production of Oxidized Graphene.

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