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Ammonium metavanadate nh4vo3

Manufactured by Merck Group
Sourced in United States

Ammonium metavanadate (NH4VO3) is a chemical compound used in various laboratory applications. It serves as a source of vanadium and is often employed in analytical and catalytic processes. The core function of ammonium metavanadate is to provide vanadium in a readily available form for use in scientific experiments and analyses.

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8 protocols using ammonium metavanadate nh4vo3

1

Synthesis of V2O5 Nanorods Using Chelating Agents

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All the chemicals were purchased from Merck and used without further purification. The vanadium oxide powders (V2O5) were synthesized using a modified sol–gel technique. Ammonium metavanadate (NH4VO3, 99.0%, Sigma-Aldrich) was first dissolved in deionized water for 2 h at 70 °C. Then, the solution of citric acid monohydrate C6H8O8 H2O (99.5%, Sigma-Aldrich) was added as the main chelating agent. Acetic acid (99.5%, Sigma-Aldrich) or ethylene glycol (99%, Sigma-Aldrich) was added as the second chelating agent. The solutions were then mixed and stirred for 3 h at 70 °C. To remove the residual water from the solutions and achieve a transparent gel, the evaporation process was applied. The xerogels (pre-heated powder) were dried in air for 12 h at 150 °C and ground in agate mortar. In the last step, the powders were heated in air from room temperature to 560 °C for 12 h and kept at 560 °C for 5 h. The sample obtained only using citric acid as the main chelating agent was labelled 'VO@1'. The powder synthesized with two chelating agents: citric with Acetic acids and citric acid with ethylene glycol was labelled 'VO@2' and 'VO@3', respectively. Figure 1, shows the schematic representation of the synthesis process used in the present case.

Schematic representation of the V2O5 nanorods preparation using different chelating agent.

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2

Vanadium-based Nanocomposite Synthesis

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All chemicals were analytical grade and used
as received. Ammonium metavanadate (NH4VO3)
(99%, Sigma Aldrich), ethanol (J.T. Baker), poly(vinylpyrrolidone)
(PVP) (Sigma Aldrich), anhydrous dimethylformamide (DMF) (99.8%, Sigma
Aldrich), oxalic acid dihydrate (H2C2O4·2H2O) (Scharlau).
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3

Photocatalytic Degradation of Methyl Orange

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Analytical grade ammonium metavanadate (NH4VO3) ≥ 99.0%, cetyl trimethyl ammonium bromide (CTAB) ≥ 98%, sodium hydroxide (NaOH) ≥ 98%, methyl orange (MO) 85%, benzoquinone (BQ) ≥ 98%, triethanolamine (TEA) ≥ 99%, and isopropyl alcohol (IPA) ≥ 99.7% were purchased from Sigma-Aldrich (St. Louis, MO, USA). All other chemicals and reagents were analytical grade and used without further purification. All the required solutions were prepared with distilled water.
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4

Synthesis and Degradation of Nanomaterials

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Bismuth nitrate pentahydrate (Bi(NO3)3·5H2O, Sigma Aldrich 99%), ammonium metavanadate (NH4VO3, Sigma Aldrich 99%), chloroauric acid (HAuCl4, Sigma Aldrich 99%), sodium borohydride (NaBH4, Sigma Aldrich 99%) and deionized water (99.99%, PAEC PK) were used for synthesis, without any further purification. Crystal violet dye (C25H30ClN3, Sigma Aldrich 99%) was used for degradation.
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5

Ammonium Metavanadate and PACAP Protocol

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Ammonium metavanadate NH4VO3 was purchased from Sigma (St. Louis, MO, USA). The 38-amino acid form of PACAP was generously provided by Professor A. Fournier.
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6

Synthesis of Cesium Vanadate Nanoparticles

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Cesium nitrate [CsNO3] (Sigma-Aldrich, Seoul, South Korea; high purity grade), ammonium metavanadate [NH4VO3] (Sigma-Aldrich, high purity grade), 1-octadecene [CH3(CH2)15CH=CH2] (Sigma-Aldrich; technical grade, 90%), oleylamine [CH3(CH2)7CH=CH(CH2)7CH2NH2] (Sigma-Aldrich; technical grade, 70%), oleic acid [CH3(CH2)7CH=CH(CH2)7COOH] (Daejung, Sinan, South Korea; extra pure), ammonium hydroxide solution [NH4OH] (Sigma-Aldrich; ~25% NH3 basis), and acetone [CH3COCH3] were of analytical grade. Triple-distilled de-ionized (DI) water was used to dissolve the CsNO3. All the above-mentioned reagents were used without additional purification.
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7

Synthesis and Characterization of Vanadium Cluster V15

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Ammonium metavanadate (NH4VO3, 99%) and D-mannitol (C6H14O6, 98%), both from Sigma-Aldrich® (St. Louis, MO, USA), and tetramethylammonium chloride (C4H12ClN, 98%) from Fluka® were used without purification. Deuterium oxide (D2O, 99.9 atom %D) was purchased from Oakwood Chemical and used as received. Ultrapure water (18.2 mΩ·cm) was used in the synthesis and characterization of V15, excepted when otherwise stated. The 51V NMR data were collected on a Bruker NEO 400 MHz spectrometer with a 105.2 MHz frequency for vanadium at 298 K, using 4096 scans in the f1 domain, 8 steady-state transitions, a spectra width of 800 ppm, a transmitter frequency offset of −548 ppm, 0.01 s relaxation delay, a 0.08192 s acquisition time, and a 16 μs pulse. Fourier-transform infrared (IR) spectra (400 to 4000 cm–1) were recorded from KBr pellets on a Bruker VERTEX-70 spectrometer with a resolution of 4 cm−1. Electron paramagnetic resonance in X-band (EPR) spectra (9.5 GHz) were recorded at 77 K on an X-band (9.5 GHz) Bruker EMX-Micro spectrometer using a pulverized sample. Electronic absorption spectra of 0.250 mmol L−1 aqueous solution of V15 were observed from 340 to 900 nm, using an AvaLight UV-Vis/NIR light source and an AvaSpex-UL S2048 Fiber-Optic Spectrometer.
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8

Synthesis of Silver-based Microcrystals

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Silver tungstate, silver molybdate, and silver vanadate were prepared as previously described (Fabbro et al., 2016 (link); Foggi et al., 2017a (link); Oliveira et al., 2017 (link)). Briefly, 1 × 10−3 mol of silver nitrate (AgNO3; 99.98% purity; Cennabras, Guarulhos, SP, Brazil) was diluted in 50 mL of distilled water. Simultaneously, 5 × 10−4 mol of sodium tungstate dihydrate (Na2WO4•2H2O; 99.99% purity; Sigma-Aldrich, St. Louis, MO, United States) or sodium molybdate dihydrate (Na2MoO4•2H2O; 99.98% purity; Alfa Aesar, Haverhill, MA, United States) or 1 × 10−3 mol of ammonium metavanadate (NH4VO3; 99.99% purity; Sigma-Aldrich, St. Louis, MI, United States) were diluted in 50 mL of distilled water. Temperatures of 70°C for α-Ag2WO4 and β-Ag2MoO4 and 10°C for α-AgVO3 were used. After reaching the temperatures required, the solutions were mixed, instantly forming a precipitate. These precipitates were washed with distilled water to a pH of 7 and oven-dried at 60°C for 12 h. After synthesis, all microcrystals were diluted in PBS to 2 mg/mL (stock solution), and the samples were maintained in the dark and at room temperature until further use.
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