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Natural graphite flake

Manufactured by Merck Group
Sourced in United States, United Kingdom

Natural graphite flakes are a type of laboratory equipment used in various scientific and industrial applications. They are composed of naturally occurring crystalline carbon material with a flaky, layered structure. The core function of natural graphite flakes is to serve as a versatile and reliable material for various experimental and analytical purposes, providing a consistent and stable performance.

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19 protocols using natural graphite flake

1

Synthesis of Silver-Reduced Graphene Oxide

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GO sheets were obtained from natural graphite flakes (99%, Aldrich) using the modified Hummers and Offman method. 50 mg of GO was dispersed in 50 mL of deionized water via sonication treatment for 60 min at room temperature, and resulting GO sheets were stripped to be single sheet structure, affording a brown liquid, which contributed to AgNPs adsorption on the surface of GO sheet. Then, 0.01, 0.1, or 1 mmol of a AgNO3 solution was added to the graphene solution, followed by NaBH4 as the reducing agent, and the resulting mixture was stirred at a speed of 1500 rpm at 25 °C for 1 h, producing Ag-GO nanoparticles. This procedure was performed in a photo area, which can prevent the decomposition of AgNO3. Then, 10 mL of a solution of ascorbic acid, which is an innocuous green reducing agent, was introduced to the solution of silver-modified GO. In order to enhance the reduction effect, the reaction was stirred at a speed of 1500 rpm at 95 °C for 1 h. In order to remove impurities from the solution, it was washed repeatedly using deionized water, and then filtered. Ag-rGO powders were obtained after drying in a vacuum oven at 25 °C for 24 h.
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2

Scalable Graphene Oxide Production

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Tens of grams of CMG were reproducibly and safely prepared using a modified Tour et al.26 (link) synthesis in a custom-built rig designed to manipulate up to 10 l of concentrated acids. In a typical synthesis, a 9:1 mixture of concentrated H2SO4/H3PO4 (3:0.3 l) was added to 24 g of natural graphite flakes (150–500 μm sieved, Aldrich), followed by the addition of 144 g of KMnO4 (6 wt. equiv.). This reaction was slightly exothermic and the temperature rose to 35–40 °C. The reacting suspension was then heated to 50 °C and vigorously stirred at 400 rpm for 18 h. Next, it was cooled to room temperature and the oxidation was stopped by adding dropwise 1.72 l of aqueous H2O2 (2 wt.%). The graphene oxide suspension was washed using repeated centrifugation at 9,000 rpm (Thermo Scientific Sorvall LYNX 6000 Superspeed Centrifuge) and redispersion in double-distilled water. The work-up was carried out until the supernatant water of the centrifuged CMG was close to pH 6, typically occurring after 16 washing cycles. Low speed (<1,000 r.p.m.) centrifugation cycles were performed to remove any un-exfoliated graphite particles.
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3

Electrochemical Sensing of Biomolecules

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N-isopropylacrylamide (NIPAm), N,N’-methylenebisacrylamide (BIS), ammonium persulfate (APS), and N,N,N’,N’-tetramethylethylenediamine (TEMED), dopamine (DA), uric acid (UA), and ascorbic acid (AA) were purchased from J&K Scientific Ltd. (Beijing, China). Carboxymethyl chitosan (CMC, degree of substitution greater than 80%), hydrogen peroxide (H2O2, 30% aqueous solution), disodium hydrogen phosphate (Na2HPO4), and sodium dihydrogen phosphate (NaH2PO4) were obtained from Beijing Chemicals Co., Ltd. (Beijing, China). Natural graphite flakes (99.8% purity) were purchased from Sigma-Aldrich (Milwaukee, WI, USA).
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4

Synthesis of Graphene Oxide-based Photocatalysts

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GO was prepared via modified Hummers method. Typically, 5 g natural graphite flakes (Sigma Aldrich) and 3.0 g NaNO3 was added to a 1000 mL beaker containing 150 mL concentrated sulphuric acid in an ice-bath and stirred for 1 h. Then 20 g KMnO4 was gradually added while stirring, keeping the temperature below 30 °C. The mixture was stirred at room temperature for 24 h. Next, the beaker was placed in an ice bath and 300 mL DI water slowly added to the beaker, keeping the reaction temperature below 98 °C. After that, 30 mL H2O2 (30%) was added to the end reaction. Once H2O2 was added, the colour of the suspension turned bright yellow. The suspension was stirred for 30 min and then centrifuged at 8000 rpm to remove large flakes, then washed with 10% HCl solution, followed by washing with DI water and a three-week dialysis. Then Ag/Ag2S–TiO2 NRs with substrates were immersed in this solution for few seconds. The samples were dried in a muffle furnace at 50 °C for 2 hours to obtain the GO/Ag/Ag2S–TiO2 NRAs photocatalyst. GO–TiO2 NRAs, GO/Ag–TiO2 NRAs, GO/Ag2S–TiO2 NRAs were prepared in the similar way. The typical procedure were illustrated in Fig. 1(a).
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5

Graphene Oxide Synthesis via Modified Hummer's Method

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Natural graphite flakes were purchased from Sigma-Aldrich (St. Louis, MO, USA). The graphene oxide used in this work was synthesized according to Hummer’s method with modifications [38 (link)]. Briefly, 5.0 g of graphite and 3.75 mg of NaNO3 were mixed in a round bottom flask containing 370 mL of H2SO4 for 20 min under magnetic stirring in an ice bath. 22.5 g of KMnO4 in 300 mL of ultrapure water was slowly added and the mixture reaction was kept stirring for 72 h at room temperature. Then, the mixture was stirred for another 1 h at 95 °C. After the temperature reduced to 60 °C, H2O2 (15 mL, 30%) was added and the solution was left to stand overnight at room temperature. The mixture was centrifuged at 6000 rpm for 15 min and rinsed with 1.0 L of an aqueous solution of H2SO4 (3%) and H2O2 (0.5%) to remove oxidant ions and inorganic impurities. The resulting product was dialyzed against ultrapure water for 72 h. The graphene oxide dispersion was lyophilized and stored in a glass desiccator at room temperature.
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6

Graphite Oxide Synthesis and Antibacterial Evaluation

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Natural graphite flakes, concentrated sulfuric acid (98%), potassium permanganate, 30% hydrogen peroxide, concentrated hydrochloric acid (98%) and ultrapure water were purchased from Sigma-Aldrich, Malaysia. All of the aqueous solutions were prepared in deionized water. Analytical grade absolute ethanol, NaCl, peptone, yeast extract, beef extract, agar were purchased from Merck, Germany. Antibacterial discs: azithromycin (AZM), gentamycin (GEN), ciprofloxacin (CIP), cefixime (CFM), amoxicillin (AMX), cotrimoxazole (COT), imipenem (IPM) and ceftriaxone (CTR) were bought from Himedia Laboratories, India. 6X loading dye, 1 Kb plus DNA ladder and Presto Blue dye were purchased from Thermo Fisher Scientific. Human serum and bacterial strains collected from urine were obtained from North East Medical College Hospital, Sylhet, Bangladesh (https://www.nemc.edu.bd/pathology-department/) following all the ethical conditions and legislations approved by the ethical committee with the Ref. No. NEMC/Sylhet/287/2013 [24 ].
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7

Synthesis of Graphene Oxide from Graphite

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Natural graphite flakes (99%; −325 mesh), tris(hydroxymethyl)aminomethane (tris base, ≥99.8%), dopamine hydrochloride (DA, 98%), and sodium hydroxide (NaOH, >97%) were purchased from Sigma Aldrich® (Munich, Germany). Sulfuric acid (H2SO4, 98%), potassium permanganate (KMnO4, ≥99%), and hydrochloric acid (HCl, 10% v/v) were received from VRW® (Darmstadt, Germany). Hydrogen peroxide (H2O2, 30% w/v) was purchased from Merck (Darmstadt, Germany). Distilled water (DW) was used in all chemical treatments.
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8

Graphite-Based Composite Materials Synthesis

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Sulfanilic acid was purchased from TCI (Shanghai) Development Co., Ltd., (Shanghai, China). Natural graphite flakes were purchased from Sigma-Aldrich (St. Louis, MO, USA). Sodium carbonate, concentrated hydrochloric acid, sodium borohydride, hydrazine (80%, N2H4·H2O), and sodium nitrite were purchased from Beijing Chemical Works. Polyacrylonitrile (PAN, average Mw 150,000) was purchased from HuBei ChuShengWei Chemistry Co., Ltd., (Wuhan, China).
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9

Graphite Flake Procurement and Characterization

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Natural graphite flakes were purchased from Sigma Aldrich. All other reagents are analytical grade chemicals.
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10

Graphene Oxide Synthesis and Freeze-Drying

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A suspension of graphene oxide was prepared via a modified Tour et al. (Marcano et al. 2010 (link)) synthesis in a custom-built rig, using natural graphite flakes (150–500 µm, Sigma-Aldrich). This was freeze-dried using a Powerdry LL1500 freeze dryer (Thermo Scientific, UK).
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