Relevant bibliographies by topics / Graphite oxide

Academic literature on the topic 'Graphite oxide'

Author: Grafiati
Published: 4 June 2021
Last updated: 4 May 2024

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Journal articles on the topic "Graphite oxide"

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Yao, Yu Qin, Yin Jie Cen, Richard D. Sisson, and Jian Yu Liang. "A Synthesize Protocol for Graphene Nanosheets." Materials Science Forum 880 (November 2016): 3–6. http://dx.doi.org/10.4028/www.scientific.net/msf.880.3.

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Chemical synthesis is cheap and easy to be tailored. Reduction of graphite oxide to form graphene nanosheets is a necessary step that determines yield, quality, chemical and surface properties of graphene nanosheets. In this report, the reduction of graphite oxides by chemical and thermal methods has been employed to convert graphite oxide synthesized by the same wet chemical method using KMnO4 and H2O2. The characterization results from the two reduction methods indicate that a combination of wet oxidation of graphite and thermal reduction method is an efficient and environmental friendly way to produce graphene.
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Li, Jinghao, Qiangu Yan, Xuefeng Zhang, Jilei Zhang, and Zhiyong Cai. "Efficient Conversion of Lignin Waste to High Value Bio-Graphene Oxide Nanomaterials." Polymers 11, no. 4 (April 4, 2019): 623. http://dx.doi.org/10.3390/polym11040623.

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Lignin graphene oxide was oxidized after Kraft lignin was graphitized by thermal catalytic conversion. The reduced lignin graphene oxide was derived from lignin graphene oxide through thermal reduction treatment. These Kraft lignin, lignin graphite, lignin graphene oxide, and reduced lignin graphene oxide were characterized by scanning electron microscopy, raman microscopy, high-resolution transmission electron microscopy, X-ray diffraction, Fourier transform infrared spectroscopy, atomic force microscopy and thermogravimetric analysis. The results showed lignin graphite converted from Kraft lignin had fewer layers with smaller lateral size than natural graphite. Moreover, lignin graphene oxide was successfully produced from lignin graphite by an oxidation reaction with an hour-long reaction time, which has remarkably shorter reaction time than that of graphene oxide made from natural graphite. Meanwhile, this lignin-derived graphene oxide had the same XRD, FTIR and Raman peaks as graphene oxide oxidized from natural graphite. The SEM, TEM, and AFM images showed that this lignin graphene oxide with 1–3 average layers has a smaller lateral size than that of graphene oxide made from natural graphite. Moreover, the lignin graphene oxide can be reduced to reduced lignin graphene oxide to fabricate graphene-based aerogel, wire, and film for some potential applications.
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Cao, Ning, and Yuan Zhang. "Study of Reduced Graphene Oxide Preparation by Hummers’ Method and Related Characterization." Journal of Nanomaterials 2015 (2015): 1–5. http://dx.doi.org/10.1155/2015/168125.

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As a novel two-dimensional carbon material, graphene has fine potential applications in the fields of electron transfer agent and supercapacitor material for its excellent electronic and optical property. However, the challenge is to synthesize graphene in a bulk quantity. In this paper, graphite oxide was prepared from natural flake graphite by Hummers’ method through liquid oxidization, and the reduced graphene oxide was obtained by chemical reduction of graphene oxide using NH3·H2O aqueous solution and hydrazine hydrate. The raw material graphite, graphite oxide, and reduced graphene oxide were characterized by X-ray diffraction (XRD), attenuated total reflectance-infrared spectroscopy (ATR-IR), and field emission scanning electron microscope (SEM). The results indicated that the distance spacing of graphite oxide was longer than that of graphite and the crystal structure of graphite was changed. The flake graphite was oxidized to graphite oxide and lots of oxygen-containing groups were found in the graphite oxide. In the morphologies of samples, fold structure was found on both the surface and the edge of reduced graphene oxide.
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Muzyka, Roksana, Sabina Drewniak, Tadeusz Pustelny, Marcin Sajdak, and Łukasz Drewniak. "Characterization of Graphite Oxide and Reduced Graphene Oxide Obtained from Different Graphite Precursors and Oxidized by Different Methods Using Raman Spectroscopy Statistical Analysis." Materials 14, no. 4 (February 6, 2021): 769. http://dx.doi.org/10.3390/ma14040769.

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In this paper, various graphite oxide (GO) and reduced graphene oxide (rGO) preparation methods are analyzed. The obtained materials differed in their properties, including (among others) their oxygen contents. The chemical and structural properties of graphite, graphite oxides, and reduced graphene oxides were previously investigated using Raman spectroscopy (RS), X-ray photoelectron spectroscopy (XPS), and X-ray diffraction (XRD). In this paper, hierarchical clustering analysis (HCA) and analysis of variance (ANOVA) were used to trace the directions of changes of the selected parameters relative to a preparation method of such oxides. We showed that the oxidation methods affected the physicochemical properties of the final products. The aim of the research was the statistical analysis of the selected properties in order to use this information to design graphene oxide materials with properties relevant for specific applications (i.e., in gas sensors).
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Liu, Hong Bo, Wu Ying Zhang, Feng Lin, and Hong Da Cao. "Comparison and Characterization of Two Preparation Methods of Graphene Oxide." Advanced Materials Research 989-994 (July 2014): 125–29. http://dx.doi.org/10.4028/www.scientific.net/amr.989-994.125.

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The graphene oxides were prepared form graphite by thermal expansion and ultrasonic dispersion. The structure of graphene oxides was characterized by Fourier transform infrared spectrometer (FTIR), scanning electron microscope (SEM), X-ray diffraction (XRD) and Raman spectra. The difference of structure of graphene oxides by two preparation methods was compared. The measurement of FTIR and XRD showed the graphite was completely oxidized. The graphene oxide prepared by thermal expansion would lose large number of active functional groups, such as hydroxyl, carboxyl group, et al. However, the graphene oxide prepared by ultrasonic dispersion can retain these active functional groups. These active functional groups will be benefit to chemically modify the graphene oxides and prepare the polymer/graphene nanocomposites.
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Yıldız, Kübra, and Muhammet Uzun. "Obtaining of Reduced Graphene Oxide from Graphite by using Hummer’s and Chemical Reduction Method." Academic Perspective Procedia 2, no. 3 (November 22, 2019): 601–5. http://dx.doi.org/10.33793/acperpro.02.03.59.

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In this study, graphene oxide (GO) was synthesized from graphite using modified Hummers method. According to other methods known in the literature, modified Hummers method; it is simpler and less costly in terms of process steps. In addition, it is safer and environmentally friendly than the Hummers method. Reduced Graphene Oxide (RGO) was obtained by reduction of graphene oxides (GO) synthesized by modified Hummers method. It is understood from the obtained results that GO is synthesized successfully from graphite powder by modified Hummers method and RGO is obtained successfully by reduction of graphene oxides (GO).
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Said, Muhammad, Maria Ulfa, Addy Rachmat, Desnelli, and Poedji Loekitowati Hariani. "Synthesis of Reduced Graphene Oxide from Cellulose and its Applications for Methylene Blue Adsorption." Solid State Phenomena 345 (July 28, 2023): 153–70. http://dx.doi.org/10.4028/p-n4sufo.

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This paper reports the synthesis and its application to the adsorption of methylene blue dye using graphene-oxide (GO) and reduced graphene-oxide (RGO). Among carbon-based nanomaterials, graphene and its derivatives have received remarkable attention due to their unique thermal, mechanical, and electronic properties and two-dimensional structure. The GO was synthesized by the modified Hummers method (chemical exfoliation) of graphite flake. This reaction produced graphite oxide (GrO) as an intermediate material. The synthesized materials, namely graphite, graphene oxide, and reduced graphene oxide, were characterized by XRD, FTIR, and Raman spectroscopy. These materials were tested to evaluate their adsorption capacity, concentration, contact time, and adsorbent weight on methylene blue, which was analyzed using a UV-vis spectrophotometer. The XRD pattern showed the formation of 2θ peaks at 24° to 26o for graphite, graphene oxide, and reduced graphene oxide, respectively. Furthermore, characterization by FTIR showed the appearance of O-H groups with peaks of 3358 cm-1 and 3342 cm-1 for graphene and reduced graphene oxides. Raman characterization indicated that reduced graphene oxide has a wavelength at the D-band peak of about 1375 cm-1 and the G-band peak reaching 1597 cm-1 with an ID/IG intensity ratio of 0.8. The adsorption test of methylene blue showed that reduced graphene oxide had the best adsorption capacity with an adsorbent, concentration, optimum time, and highest adsorption capacity value of 25 mg, 30 ppm, 45 minutes, and 15.642 mg/g. The adsorption process followed the Langmuir isotherm rule, as evidenced by the R2 value of 0.9881.
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Minitha, Cherukutty Ramakrishnan, and Ramasamy Thangavelu Rajendrakumar. "Synthesis and Characterization of Reduced Graphene Oxide." Advanced Materials Research 678 (March 2013): 56–60. http://dx.doi.org/10.4028/www.scientific.net/amr.678.56.

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Reduced graphene oxide is an excellent candidate for various electronic devices such as high performance gas sensors. In this work Graphene oxide was prepared by oxidizing graphite to form graphite oxide. From XRD analysis the peak around 11.5o confirmed that the oxygen was intercalated into graphite. By using hydrazine hydrate, the epoxy group in graphite oxide was reduced then the solution of reduced graphite oxide (rGO) is exfoliated. Raman spectrum of rGO contains both G band (1580 cm-1), D band (1350 cm-1). The remarkable structural changes reveals that reduction of graphene oxide from the values of ID/IG ratio that increase from 0.727 (GO) to 1.414 (rGO). The exfoliated reduced graphite oxide solution is spin coated on to the SiO2/Si substrates.
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Corso, Marla, Ana Carolina de Dias Albuquerque, Lídia Pereira Amaro, Lilian Keylla Berto, Silvia Luciana Favaro, Hugo Eiji Imai, Adriano Pereira Cardoso, Natália Ueda Yamaguchi, and Luciana Cristina Soto Herek Rezende. "Graphene oxide synthesis for composite material preparation." Revista Ibero-Americana de Ciências Ambientais 10, no. 1 (June 20, 2019): 157–66. http://dx.doi.org/10.6008/cbpc2179-6858.2019.001.0013.

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Graphene, a material formed by carbon atoms with sp2 hybridization in a hexagonal arrangement, has differentiated characteristics in comparison to commercial materials such as high flexibility, high electrical and thermal conductivity, and strong resistance due to the organized structure of the material and can be applied in several branches of research. The best-known method for the production of graphene is the exfoliation of graphite using the methodology proposed by Hummers, in which the commercial graphite is oxidized obtaining as final product the graphene oxide that can be converted into graphene. In this study, the Hummers methodology was used in the oxidation of synthetic graphite and graphene nanoplates of 5 μm and 15 μm. The obtained materials were characterized by FTIR, RAMAN and XRD, allowing to observe the best synthesis to be used in the production of graphene oxide. Then, composites were prepared using the graphene oxides obtained as filler. In order to obtain them, different mass quantities of graphene oxides (1%, 3% and 5% in relation to the polypropylene polymer matrix) were used, demonstrating by the strain tensile stress tests that the composite materials have results more satisfactory than pure polypropylene.
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Yu, Hui Jiang, Zheng Guang Zou, Fei Long, Chun Yan Xie, and Hao Ma. "Preparation of Graphene with Ultrasound-Assisted in the Process of Oxidation." Applied Mechanics and Materials 34-35 (October 2010): 1784–87. http://dx.doi.org/10.4028/www.scientific.net/amm.34-35.1784.

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To get single-layer of graphene, exfoliating fully intercalated graphite oxide into single- layer graphene oxide is one of the important factors. In this paper, graphite oxide prepared by the Improved Hummers Method, and ultrasound was added to the Low-temperature Reaction of this oxidation process to improve the efficiency of intercalation. Then the obtained graphene oxide was dispersed with surfactant and reduced with Hydrazine Hydrate. XRD patterns indicated that the layer distance of graphite oxide did increased at the aid of the ultrasound, and the obtained reduced products were single- and few-layer. FT-IR analysis further confirmed the preparation of graphite oxide and graphene.
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Dissertations / Theses on the topic "Graphite oxide"

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Sokolov, Denis A. "Investigation of Graphene Formation from Graphite Oxide and Silicon Carbide." Diss., Georgia Institute of Technology, 2013. http://hdl.handle.net/1853/53642.

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Graphene is a novel two dimensional material that is revolutionizing many areas of science and it is no surprise that a significant amount of effort is dedicated to its investigation. One of the major areas of graphene research is the development of procedures for large scale production. Among many recently developed methodologies, graphene oxide reduction stands out as a straightforward and scalable procedure for producing final material with properties similar to those of graphene. Laser reduction of graphite oxide is one of the novel approaches for producing multilayer graphene, and this work describes a viable approach in detail. It is determined that a material which is comprised of a combination of laser reduced graphite oxide-coupled to an unreduced graphite oxide layers beneath it, produces a broadband photosensitive material. The efficiency of light conversion into electrical current is greatly dependent upon the oxygen content of the underlying graphite oxide. Developing novel ways for reducing graphite oxide is an ongoing effort. This work also presents a new method for achieving complete reduction of graphite oxide for producing predominantly sp2 hybridized material. This approach is based on the irradiation of graphite oxide with a high flux 3 keV Ar ion beam in vacuum. It is determined that the angle of irradiation greatly influences the final surface morphology of reduced graphite oxide. Also, multilayer epitaxial graphene growth on silicon carbide in ultra-high vacuum was investigated with quadrupole mass spectrometry (QMS). Subliming molecular and atomic species were monitored as a function of temperature and heating time. The grown films were characterized with X-ray photoelectron spectroscopy coupled with Ar ion depth profiling.
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Arbuzov, A. A., V. E. Muradyan, and B. P. Tarasov. "Synthesis of Few-layer Graphene Sheets via Chemical and Thermal Reduction of Graphite Oxide." Thesis, Sumy State University, 2012. http://essuir.sumdu.edu.ua/handle/123456789/35063.

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Few-layer graphene sheets were produced from graphite oxide (GO) chemical and thermal reduction. For the chemical reduction of GO as reducing agents were used hydrazine hydrate, hydroxylammonium chloride, sodium borohydride and sodium sulfite. The reduced material was characterized by elemental analysis, thermo-gravimetric analysis, scanning electron microscopy, X-ray diffraction, Fourier transform infrared and Raman spectroscopy. A comparison of the deoxygenation efficiency of graphene oxide suspension by different method or reductants has been made, revealing that the highest degree of reduction was achieved by thermal reduction and using hydrazine hydrate and hydroxylammonium chloride as a reducing agents. When you are citing the document, use the following link http://essuir.sumdu.edu.ua/handle/123456789/35063
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Nyangiwe, Nangamso Nathaniel. "Graphene based nano-coatings: synthesis and physical-chemical investigations." Thesis, UWC, 2012. http://hdl.handle.net/11394/3237.

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Magister Scientiae - MSc
It is well known that a lead pencil is made of graphite, a naturally form of carbon, this is important but not very exciting. The exciting part is that graphite contains stacked layers of graphene and each and every layer is one atom thick. Scientists believed that these graphene layers could not be isolated from graphite because they were thought to be thermodynamically unstable on their own and taking them out from the parent graphite crystal will lead them to collapse and not forming a layer. The question arose, how thin one could make graphite. Two scientists from University of Manchester answered this question by peeling layers from a graphite crystal by using sticky tape and then rubbing them onto a silicon dioxide surface. They managed to isolate just one atom thick layer from graphite for the first time using a method called micromechanical cleavage or scotch tape. In this thesis chemical method also known as Hummers method has been used to fabricate graphene oxide (GO) and reduced graphene oxide. GO was synthesized through the oxidation of graphite to graphene oxide in the presence of concentrated sulphuric acid, hydrochloric acid and potassium permanganate. A strong reducing agent known as hydrazine hydrate has also been used to reduce GO to rGO by removing oxygen functional groups, but unfortunately not all oxygen functional groups have been removed, that is why the final product is named rGO. GO and rGO solutions were then deposited on silicon substrates separately. Several characterization techniques in this work have been used to investigate the optical properties, the morphology, crystallography and vibrational properties of GO and rGO.
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Lee, Dongwook. "The structure and magnetism of graphite oxide." Thesis, University of Cambridge, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.611649.

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Li, Wei. "Composite polymer/graphite/oxide electrode systems for supercapacitors." University of Cincinnati / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1439309266.

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Arbuzov, A. A., V. E. Muradyan, B. P. Tarasov, and E. A. Sokolov. "Preparation of Amino-Functionalized Graphene Sheets and their Conductive Properties." Thesis, Sumy State University, 2013. http://essuir.sumdu.edu.ua/handle/123456789/35639.

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Amino-functionalized graphene sheets were prepared through chemical reduction by hydrazine hy-drate, amination or amidation of graphite oxide. For amination of graphite oxide were used polyamine such as ethylenediamine, diethylenetriamine and triethylenetetramine. Addition of amine groups to graphene is identified by Fourier transform infrared spectroscopy, Raman spectroscopy, elemental analysis and ther-mogravimetry. Scanning electron microscopy data indicate that the organic amine is not only as nitrogen sources to obtain the nitrogen-doped graphene but also as an important modification to control the assem-bly of graphene sheets in the 3D structures. The electrical conductivity of the materials obtained by amina-tion and amidation of graphene is much smaller than that of reduced graphite oxide. When you are citing the document, use the following link http://essuir.sumdu.edu.ua/handle/123456789/35639
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Jiang, San-Ping. "A study of teflon-bonded cobalt oxide/graphite electrodes." Thesis, City University London, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.306058.

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Shulga, Y. M., S. A. Baskakov, E. I. Knerelman, G. I. Davidova, E. R. Badamshina, S. Y. Shulga, E. A. Skrileva, A. L. Agapov, D. N. Voylov, and A. P. Sokolov. "Carbon Nanomaterial Produced by Microwave Exfoliation of Graphite Oxide." Thesis, Sumy State University, 2013. http://essuir.sumdu.edu.ua/handle/123456789/35118.

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Carbon-based graphene-like material was obtained through microwave stimulated exfoliation of graph-ite oxide (GO). Properties of this material were investigated by multiple techniques including element analysis, X-ray photoelectron spectroscopy (XPS), mass-spectroscopy, infrared (IR) and Raman spectrosco-py, scanning electron microscopy (SEM) and broadband dielectric spectroscopy. Specific surface area and volume of microwave exfoliated graphite oxide (MEGO) reached 600 m2/g and 6 cm3/g, respectively. It is shown that during such explosive reduction process the sample emits CO2, CO and H2O and, in some cases, SO2 gases. The resulting reduced material exhibits IR spectra similar to that of graphite and a dc-conductivity of 0.12 S/cm. It is also shown that prolonged storage in ambient conditions leads to elevated oxygen content and decrease of specific surface area of the samples. When you are citing the document, use the following link http://essuir.sumdu.edu.ua/handle/123456789/35118
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Mowry, Michael N. "In situ Raman Spectroscopy Study of the Formation of Graphene from Urea and Graphite Oxide." Thesis, Monterey, California. Naval Postgraduate School, 2012. http://hdl.handle.net/10945/17424.

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Approved for public release; distribution is unlimited
Graphene, 10 or fewer atomic layers of carbon atoms, has attracted much attention during recent years due to its unique structure and exceptional physical properties. While there exist a wide range of potential applications, as with many nanomaterials, new synthesis techniques are required that allow for a production of graphene on an industrial scale. In this study, in situ Raman spectroscopy was used to study the formation and doping of graphene during urea-assisted thermal exfoliation of graphite oxide (GO), a promising new synthesis method that can be scaled to industrial levels. Thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and mass spectroscopy were used complementary to Raman spectroscopy to assist with the interpretation of the obtained data. Raman spectroscopy is a powerful characterization tool for the analysis of carbon nanomaterials, such as graphene. While several researchers have reported on the reaction of urea and GO, none of the studies found in literature has provided deeper insights on the evolution of the graphene structure and the simultaneous incorporation of nitrogen into the honeycomb lattice during synthesis. The knowledge gained from this work allows for a better understanding of the graphene production process and provides further evidence for the potential nitrogen-doping of graphene via deposition of urea.
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Leve, Zandile Dennis. "Determination of paracetamol at the electrochemically reduced graphene oxide-metal nanocomposite modified pencil graphite (ERGO-MC-PGE) electrode using adsorptive stripping differential pulse voltammetry." University of Western Cape, 2020. http://hdl.handle.net/11394/7350.

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>Magister Scientiae - MSc
This project focuses on the development of simple, highly sensitive, accurate, and low cost electrochemical sensors based on the modification of pencil graphite electrodes by the electrochemical reduction of graphene oxide-metal salts as nanocomposites (ERGO-MC-PGE; MC = Sb or Au nanocomposite). The electrochemical sensors ERGO-Sb-PGE and ERGO-Au-PGE were used in the determination of paracetamol (PC) in pharmaceutical formulations using adsorptive stripping differential pulse voltammetry. The GO was prepared from graphite via a modified Hummers’ method and characterized by FTIR and Raman spectroscopy to confirm the presence of oxygen functional groups in the conjugated carbon-based structure whilst, changes in crystalline structure was observed after XRD analysis of graphite and GO.
2023-10-07
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Books on the topic "Graphite oxide"

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Jean, Corbin, and United States. National Aeronautics and Space Administration., eds. Synthesis and thermal stability of graphite oxide-like materials. [Washington, D.C: National Aeronautics and Space Administration, 1997.

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Fusaro, Robert L. Sputtered cadmium oxide as a surface pretreatment for graphite solid lubricant films. [Washington, DC]: National Aeronautics and Space Administration, Scientific and Technical Information Division, 1986.

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Dimiev, Ayrat M., and Siegfried Eigler, eds. Graphene Oxide. Chichester, UK: John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781119069447.

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Gao, Wei, ed. Graphene Oxide. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-15500-5.

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Zhao, Jijun, Lizhao Liu, and Fen Li. Graphene Oxide: Physics and Applications. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-44829-8.

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Pendolino, Flavio, and Nerina Armata. Graphene Oxide in Environmental Remediation Process. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-60429-9.

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Gao, Zhenghan. Phase Diagrams of Water Confined by Graphene and Graphene Oxide. [New York, N.Y.?]: [publisher not identified], 2018.

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Ezema, Fabian Ifeanyichukwu, Tingkai Zhao, and Ishaq Ahmad. Graphene Oxide in Enhancing Energy Storage Devices. Boca Raton: CRC Press, 2022. http://dx.doi.org/10.1201/9781003215196.

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Graphene nanoelectronics: From materials to circuits. New York: Springer, 2012.

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United States. National Aeronautics and Space Administration., ed. Ferric chloride graphite intercalation compounds prepared from graphite fluoride. [Washington, DC]: National Aeronautics and Space Administration, 1993.

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Book chapters on the topic "Graphite oxide"

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Gao, Wei. "Graphite Oxide." In Springer Handbook of Nanomaterials, 571–604. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-20595-8_15.

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Besenhard, J. O. "Graphite Oxide Membranes." In Inorganic Reactions and Methods, 265. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145326.ch152.

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Lerf, Anton. "Graphite Oxide Story - From the Beginning Till the Graphene Hype." In Graphene Oxide, 1–35. Chichester, UK: John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781119069447.ch1.

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Sugimoto, Wataru. "Graphene (or Reduced Graphite Oxide Nanosheets)." In Encyclopedia of Applied Electrochemistry, 954–63. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4419-6996-5_507.

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Oliva González, Cesar Máximo, Oxana V. Kharissova, Cynthia Estephanya Ibarra Torres, Boris I. Kharisov, and Lucy T. Gonzalez. "Chapter 1. Hybrids of Graphite, Graphene and Graphene Oxide." In All-carbon Composites and Hybrids, 1–30. Cambridge: Royal Society of Chemistry, 2021. http://dx.doi.org/10.1039/9781839162718-00001.

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Kumar, Pankaj, Neetu Divya, and J. K. Ratan. "Synthesis and Characterization of Chemically Derived Graphene Oxide from Graphite." In Lecture Notes in Civil Engineering, 85–94. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-6717-5_9.

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Periolatto, Monica, Elisabetta Di Francia, Marco Sangermano, Sabrina Grassini, and Pasquale Russo Spena. "Advanced Epoxy-Based Anticorrosion Coatings Containing Graphite Oxide." In Advanced Structured Materials, 135–43. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-50784-2_11.

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Jin, Wen Jie, Sei Min Park, Ik Pyo Hong, Seong Young Lee, and Myung Soo Kim. "Performance of Tin Oxide/Graphite Composite Anode for Lithium Ion Battery." In Solid State Phenomena, 1051–54. Stafa: Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/3-908451-31-0.1051.

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Guidoni, A. Giardini, A. Mele, G. Pizzella, and R. Teghil. "Metal carbide clusters formed by laser ablation of metal oxide-graphite systems." In Small Particles and Inorganic Clusters, 539–41. Berlin, Heidelberg: Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-76178-2_128.

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Saini, Priyanka, Bharti Rani, Jitendra Kumar Yadav, Piyush Choudhary, Priyambada Sahoo, and Ambesh Dixit. "Exfoliated Graphite as a Potential Host for Zinc Oxide Nanorods-Based Symmetric Flexible Supercapacitor." In Advances in Sustainability Science and Technology, 125–36. Singapore: Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-99-9009-2_11.

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Conference papers on the topic "Graphite oxide"

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Hidayah, N. M. S., Wei-Wen Liu, Chin-Wei Lai, N. Z. Noriman, Cheng-Seong Khe, U. Hashim, and H. Cheun Lee. "Comparison on graphite, graphene oxide and reduced graphene oxide: Synthesis and characterization." In PROCEEDINGS OF THE INTERNATIONAL CONFERENCE OF GLOBAL NETWORK FOR INNOVATIVE TECHNOLOGY AND AWAM INTERNATIONAL CONFERENCE IN CIVIL ENGINEERING (IGNITE-AICCE’17): Sustainable Technology And Practice For Infrastructure and Community Resilience. Author(s), 2017. http://dx.doi.org/10.1063/1.5005764.

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Rohini, Puliyasseri, and Dillibabu Sastikumar. "Synthesis and characterization of Graphite Oxide from Graphite using Nano second pulsed laser ablation in liquid." In Advanced Solid State Lasers. Washington, D.C.: Optica Publishing Group, 2022. http://dx.doi.org/10.1364/assl.2022.jtu6b.17.

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Panatarani, C., N. Muthahhari, Anton Rianto, and I. Made Joni. "Purification and preparation of graphite oxide from natural graphite." In THE 4TH INTERNATIONAL CONFERENCE ON THEORETICAL AND APPLIED PHYSICS (ICTAP) 2014. AIP Publishing LLC, 2016. http://dx.doi.org/10.1063/1.4943717.

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Jankovský, Ondřej, David Sedmidubský, Michal Lojka, and Zdeněk Sofer. "Thermal properties of graphite oxide, thermally reduced graphene and chemically reduced graphene." In INTERNATIONAL CONFERENCE OF NUMERICAL ANALYSIS AND APPLIED MATHEMATICS (ICNAAM 2016). Author(s), 2017. http://dx.doi.org/10.1063/1.4994480.

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Muzyka, R., S. Drewniak, T. Pustelny, G. Gryglewicz, and Ł. Smędowski. "RAMAN spectroscopic study of graphite oxide obtained from different graphite precursors." In 11th Integrated Optics - Sensors, Sensing Structures and Methods, edited by Tadeusz Pustelny, Przemyslaw Struk, Pawel Mergo, and Jacek Wojtas. SPIE, 2016. http://dx.doi.org/10.1117/12.2244461.

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"Graphite Nanoplatelets and Graphene Oxide Influence on C-S-H Formation." In "SP-329: Superplasticizers and Other Chemical Admixtures in Concrete Proceedings Twelfth International Conference, Beijing, China". American Concrete Institute, 2018. http://dx.doi.org/10.14359/51711218.

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Umar, Marjoni Imamora Ali, Chi Chin Yap, Rozidawati Awang, Muhamad Mat Salleh, and Muhammad Yahaya. "Effect of graphite oxide solution concentration on the properties of multilayer graphene." In THE 2013 UKM FST POSTGRADUATE COLLOQUIUM: Proceedings of the Universiti Kebangsaan Malaysia, Faculty of Science and Technology 2013 Postgraduate Colloquium. AIP Publishing LLC, 2013. http://dx.doi.org/10.1063/1.4858639.

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Amarathunga, A. A. S., M. K. A. Sadnaruwani, and H. S. Sitinamaluwa. "Mesoporous Activated Graphene Oxide based Electrochemical Capacitor from Sri Lankan Vein Graphite." In 2023 Moratuwa Engineering Research Conference (MERCon). IEEE, 2023. http://dx.doi.org/10.1109/mercon60487.2023.10355472.

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Haynes, C. E., and P. C. Rice-Evans. "Positronium at a nitric oxide monolayer on graphite." In The fifth international workshop on slow positron beam techniques for solids and surfaces. AIP, 1994. http://dx.doi.org/10.1063/1.45495.

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Panatarani, Camellia, Ayu Oktama Maulana, Anton Rianto, and I. Made Joni. "Preparation of graphite oxide by sodium cholate intercalation and sonication from Indonesian natural graphite." In 2ND PADJADJARAN INTERNATIONAL PHYSICS SYMPOSIUM 2015 (PIPS-2015): Materials Functionalization and Energy Conservations. AIP Publishing LLC, 2016. http://dx.doi.org/10.1063/1.4941908.

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Reports on the topic "Graphite oxide"

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Blanchard, Jeremy, David C. Gerlach, Randall D. Scheele, Mark L. Stewart, Bruce D. Reid, Phillip A. Gauglitz, Larry M. Bagaasen, et al. Uranium Oxide Aerosol Transport in Porous Graphite. Office of Scientific and Technical Information (OSTI), January 2012. http://dx.doi.org/10.2172/1051989.

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Sevigny, Gary J., Radha K. Motkuri, David W. Gotthold, Leonard S. Fifield, Anthony P. Frost, and Wesley Bratton. Separation of tritiated water using graphene oxide membrane. Office of Scientific and Technical Information (OSTI), June 2015. http://dx.doi.org/10.2172/1222908.

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Brossia. L52119 Comparative Consumption Rates of Impressed Current Cathodic Protection Anodes. Chantilly, Virginia: Pipeline Research Council International, Inc. (PRCI), January 2004. http://dx.doi.org/10.55274/r0010953.

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There is a variety of impressed current anode materials available for onshore applications, including High Silicon Cast Iron (HSCI), Mixed Metal Oxides (MMO), graphite, platinum (or platinum coated titanium), and conductive polymers. Many end users simply select the anode material that they have experience with. What is lacking is a clear, direct comparison of relative anode consumption rates conducted under identical conditions. The present study examined the behavior of the various anode types under different current loads and soil conditions in an effort to establish baseline consumption rates under controlled conditions. Variables that were examined included soil resistivity, the presence of coke backfill, current load, and soil type (sand or 50/50 clay/sand mix). The consumption rates of the anodes evaluated decreased in the order of: AnodeFlex, HSCI, Graphite, Pt, and MMO. A survey of field experiences yielded a slightly different order in terms of anode life with Graphite and HSCI lasting the longest. However, given the wide range of anode sizes used in the various field sites, it is difficult to directly link the field results to the consumption rates measured in the laboratory. Soil composition and resistivity were not observed to have a significant influence on anode consumption rates. The presence of coke, however, led to a decrease in consumption for all anodes in some cases by as much as a factor of nearly 70. Utilizing anode cost estimates and neglecting installation costs, the life-cycle material costs for MMO and Pt anodes are much lower than the other anode materials. Furthermore, AnodeFlex was noted to be the highest cost system from a materials perspective. This may be slightly misleading since installation and replacement costs are not factored in. Given that the installation of AnodeFlex is often much easier and less expensive than the other anode types, this may prove to be a viable financial decision when the other factors are considered. ����������� The primary implications of the present study are: Despite higher material costs, MMO and Pt anodes may offer significant long-term cost savings as compared to other anode types for many applications Use of coke backfill is critical to ensure lower anode consumption rates for AnodeFlex, Graphite, and to a lesser extent HSCI; coke does not appear necessary for MMO or Pt Soil composition (sand vs. clay/sand mix) and resistivity do not appear to significantly influence anode consumption rates, thus consideration of the soil environment (except groundwater chemistry) is not needed in selection of an appropriate anode Because the influence of groundwater chemistry (as part of the soil environment) was not examined, the effects of sulfate, chloride, and pH will need to be evaluated in detail to better aid in anode material selection Field use survey responses showed a wide range in observed anode lifespan, with graphite and HSCI experiencing the longest life and cable anodes the shortest The field survey also revealed that a significant cause of anode failures was connector and cable problems
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Mattei-Sosa, Jose, Victor Medina, Chris Griggs, and Veera Gude. Crosslinking graphene oxide and chitosan to form scalable water treatment membranes. Engineer Research and Development Center (U.S.), July 2019. http://dx.doi.org/10.21079/11681/33263.

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Mannion, J. M., R. M. Achey, J. H. Hewitt, C. R. Shick, Jr., and M. J. Siegfried. Reduced graphene oxide as a filament material for thermal ionization mass spectrometry. Office of Scientific and Technical Information (OSTI), September 2018. http://dx.doi.org/10.2172/1475282.

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Attias, Andre-Jean, Kwang-Sup Lee, and Alex K. Jen. Coupling Graphene Sheets with Iron Oxide Nanoparticles for Energy Storage and Microelectronics. Fort Belvoir, VA: Defense Technical Information Center, August 2015. http://dx.doi.org/10.21236/ada636883.

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Kichukova, Diana, Daniela Kovacheva, Anna Staneva, and Ivanka Spassova. Аntimicrobial Impact of Nanocomposites of Reduced Graphene Oxide with Silver and Copper. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, February 2021. http://dx.doi.org/10.7546/crabs.2021.02.04.

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George, Steven M. Atomic Layer Deposition of Metal Oxides on sp2-Graphitic Carbon Substrates. Fort Belvoir, VA: Defense Technical Information Center, March 2014. http://dx.doi.org/10.21236/ada608981.

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Pramanik, Avijit, Olorunsola Praise Kolawole, Kaelin Gates, Sanchita Kundu, Manoj Shukla, Robert Moser, Mine Ucak-Astarlioglu, Ahmed Al-Ostaz, and Paresh Chandra Ray. 2D fluorinated graphene oxide (FGO)-polyethyleneimine (PEI) based 3D porous nanoplatform for effective removal of forever toxic chemicals, pharmaceutical toxins, and waterborne pathogens from environmental water samples. Engineer Research and Development Center (U.S.), February 2024. http://dx.doi.org/10.21079/11681/48232.

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Although water is essential for life, as per the United Nations, around 2 billion people in this world lack access to safely managed drinking water services at home. Herein we report the development of a two-dimensional (2D) fluorinated graphene oxide (FGO) and polyethylenimine (PEI) based three-dimensional (3D) porous nanoplatform for the effective removal of polyfluoroalkyl substances (PFAS), pharmaceutical toxins, and waterborne pathogens from contaminated water. Experimental data show that the FGO-PEI based nanoplatform has an estimated adsorption capacity (𝘲ₘ) of ∼219 mg g⁻¹ for perfluorononanoic acid (PFNA) and can be used for 99% removal of several short- and long-chain PFAS. A comparative PFNA capturing study using different types of nanoplatforms indicates that the 𝘲ₘ value is in the order FGO-PEI > FGO > GO-PEI, which indicates that fluorophilic, electrostatic, and hydrophobic interactions play important roles for the removal of PFAS. Reported data show that the FGO-PEI based nanoplatform has a capability for 100% removal of moxifloxacin antibiotics with an estimated 𝘲ₘ of ∼299 mg g⁻¹. Furthermore, because the pore size of the nanoplatform is much smaller than the size of pathogens, it has a capability for 100% removal of Salmonella and Escherichia coli from water. Moreover, reported data show around 96% removal of PFAS, pharmaceutical toxins, and pathogens simultaneously from spiked river, lake, and tap water samples using the nanoplatform.
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Medina, Victor, Chandler Noel, and Jose Mattei-Sosa. Conceptual development and testing of a chitosan/graphene oxide (CSGO) “bandage” to isolate and remove chemical contamination from surfaces. Engineer Research and Development Center (U.S.), July 2019. http://dx.doi.org/10.21079/11681/33403.

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