Ferroferric oxide-carbon and nitrogen composite and preparation and application thereof
A technology of triiron tetroxide and complexes, which is applied in chemical instruments and methods, chemical/physical processes, catalyst carriers, etc., can solve the problems of easy falling off of catalyst active particles, low catalytic activity, and small specific surface area. Activity and stability, promoting catalytic oxidation, the effect of large specific surface area
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Embodiment 1
[0034] a. Fe 3 O 4 -CN x Vector preparation
[0035] (1) 2 g of ferric chloride and 5.1 g of ferrous chloride were added to tertiary distilled water, nitrogen was introduced, ammonia water was added at 60 °C to make the pH of the solution = 12, and the temperature was raised to 80 °C for 1 h under nitrogen protection. , cooled, washed, dried under vacuum for 8 h and ground to obtain nano-iron tetroxide.
[0036] (2) Add 0.2 g of nano ferric tetroxide into tertiary distilled water, ultrasonically and stir to make it fully dispersed; add 0.2 g of pyrrole monomer and 2.2 g of surfactant sodium lauryl sulfate to it, and then slowly drop Add oxidant ferric chloride solution (20 % mass concentration, 0.44g containing oxidant), react at 5 ℃ for 2 hours; after the reaction is completed, suction filter, wash, and dry at 50 ℃ to obtain ferric oxide- Carbon Nitrogen Complex Precursors.
[0037] (3) Heat treatment of the ferric oxide-carbon and nitrogen composite precursor at a temp...
Embodiment 2
[0042] a. Fe 3 O 4 -CN x Vector preparation
[0043] (1) 2.3 g of ferric chloride and 5.8 g of ferrous chloride were added to the three-distilled water, nitrogen was introduced, ammonia water was added at 60 °C to make the pH of the solution = 11, and the temperature was raised to 60 °C for 3 h under nitrogen protection. , cooled, washed, dried in vacuum for 10 h and ground to obtain nano-iron tetroxide.
[0044] (2) Add 0.23 g of nano ferric tetroxide into tertiary distilled water, ultrasonically and stir to make it fully dispersed, and add 0.26 g of pyrrole monomer and 2.4 g of surfactant octadecyltrimethylammonium bromide in turn. , and then slowly dropwise add the oxidant ferric chloride solution (the mass concentration is 25%, containing 0.55 g of oxidant), and react at a temperature of 3 °C for 2 hours. After the reaction is completed, suction filtration, wash, and dry at 60 °C. Ferric oxide-carbon-nitrogen complex precursor.
[0045] (3) Heat treatment of the ferr...
Embodiment 3
[0050] a. Fe 3 O 4 -CN x Vector preparation
[0051] (1) 3 g of ferric chloride and 6.8 g of ferrous chloride were added to the tertiary distilled water, nitrogen was introduced, ammonia water was added at 85 °C to make the pH value of the solution = 9, and the temperature was raised to 75 °C under nitrogen protection and maintained for 3 h, cooled, washed, vacuum-dried for 8 h and ground to obtain nano-iron tetroxide.
[0052] (2) Add 0.26 g of nano ferric tetroxide into tertiary distilled water, ultrasonicate and stir to make it fully dispersed; add 0.3 g of pyrrole monomer and 2.7 g of surfactant ammonium oleate in turn, and then slowly add oxidizing agent dropwise to it. Ammonium sulfate (25 % mass concentration, 0.72 g oxidant) was reacted at 0 °C for 5 hours; after the reaction was completed, suction filtration, washing, and drying at 50 °C temperature, ferric tetroxide-carbon-nitrogen complex precursor.
[0053] (3) Heat treatment of the ferric oxide-carbon and nit...
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