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Bi2o3 nanoparticles

Manufactured by Merck Group
Sourced in India

Bi2O3 nanoparticles are a type of lab equipment used in various scientific applications. They are composed of bismuth oxide and possess unique properties at the nanoscale. The core function of Bi2O3 nanoparticles is to serve as a versatile material for researchers and scientists working in fields such as catalysis, optics, and electronics. This product provides a high surface area-to-volume ratio and specific chemical characteristics that make it suitable for a range of experimental and analytical purposes.

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2 protocols using bi2o3 nanoparticles

1

Synthesis of Nanothermite Composites

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Nanothermite
composites have been prepared by ultrasonic mixing of 200 mg of Bi2O3 nanoparticles of average diameter of 90–210
nm (procured from Sigma-Aldrich, India) with 50 mg of Al nanopowder
of average diameter of 80 nm (procured from Neo Ecosystem Pvt Ltd
India) in isopropyl alcohol (30 mL) in a Sonics Vibra-Cell ultrasonic
processor (model VCX130, 130 W, 20 kHz, Sonics & Materials, Inc.).
The ultrasonication process disperses and breaks apart the agglomerates
of Bi2O3 and Al nanoparticles and promotes homogeneous
mixing. The ultrasonication process has been continued for ∼10
min in this synthesis by keeping the on–off pulsing time equal
to 10 s to avoid any thermal gradient within the solution. Finally,
the isopropyl alcohol is evaporated by drying the well-homogenized
slurry at 90 °C in a hot air oven and the dried powder is extracted
and immediately kept under vacuum to avoid any moisture absorption.
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2

Synthesis and Characterization of BLF-Loaded Nanoparticles

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BLF standard compound (99%, HPLC grade), zinc acetate anhydrous (Zn(O2CCH3)2), cetyl trimethyl ammonium bromide (CTAB) and Bi2O3 nanoparticles were obtained from Sigma Aldrich Co. NaOH, absolute ethanol and dimethyl formamide (DMF) were purchased from Fisher Scientific (India). BLF tablets (B-Cin 50 mg) were purchased from a local pharmacy shop. A stock solution of 0.01 mM BLF was prepared with methanol in a 100 mL volumetric flask and kept at 4 °C. Working solutions were prepared freshly by transferring suitable aliquots from stock solution and diluting them with BR buffer solution [37 ]. All other aqueous solutions were configured in de-ionized water (18.2 MΩ·cm) generated from Elga purification system (UK). The reagents used in experimentation were of analytical grade quality and consumed with no additional refinement.
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