Bamboo joint/coated non-noble metal SO2 electrochemical oxidation catalyst as well as preparation method and application thereof
A technology for oxidation catalysts and non-precious metals, applied in the direction of physical/chemical process catalysts, molecular sieve catalysts, chemical instruments and methods, etc., can solve the problem of high cost of electro-oxidation catalysts, and achieve mass production, mass transfer, and high ratio The effect of surface area
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Embodiment 1
[0047] Take 1g ferric ammonium citrate, add it to 20mL deionized water, the molar concentration is 0.1mol L -1 , fully stirred to disperse; take 2.4g melamine and add it to 100mL 100℃ deionized water, the molar concentration is 0.19mol L -1 , fully dissolve and stir; add ferric ammonium citrate solution into melamine solution, stir well to combine, add 0.5g NKF-11 molecular sieve, adjust temperature to 80°C, stir at constant temperature and evaporate to dryness. Put the precursor mixture into the tube furnace, Ar atmosphere, at 2 °C min -1 Rise to 600°C, keep at constant temperature for 2h; take out after cooling. At 40°C, the carbide in 1mol L -1 Stand in NaOH for 24h; wash with deionized water, then in 5% NH 4 F and CH 3 COOH mixed solution (NH 4 F and CH 3 The mass ratio of COOH is 1:1) to stand for 24h; wash and dry. Then at 10℃min -1 Rise to 700°C for secondary carbonization, and keep at constant temperature for 2 hours. Cool naturally, and grind to obtain the ca...
Embodiment 2
[0049] Take 1g ferric ammonium citrate, add it to 20mL deionized water, the molar concentration is 0.1mol L -1 , fully stirred to disperse; take 2.4g melamine and add it to 100mL 100℃ deionized water, the molar concentration is 0.19mol L -1 , fully dissolve and stir; add ferric ammonium citrate solution into melamine solution, stir well to combine, add 0.5g NKF-11 molecular sieve, adjust temperature to 80°C, stir at constant temperature and evaporate to dryness. Put the precursor mixture into the tube furnace, Ar atmosphere, at 10 °C min -1 Rise to 500°C, keep at constant temperature for 2h; take out after cooling. At 40°C, the carbide in 1mol L -1 Stand in NaOH for 24h; wash with deionized water, then in 5% NH 4 F and CH 3 Stand in the COOH mixed solution for 24h; wash and dry. Then at 10℃min -1 Rise to 700°C for secondary carbonization, and keep at constant temperature for 2 hours. Natural cooling, grinding to obtain the catalyst, its SO 2 Electrooxidation properties...
Embodiment 3
[0051] in 1g L -1 Na 2 SO 3 (H 2 SO 4 ), test the SO of the catalyst prepared by Example 1 2 Oxidation performance and compared with Pt / C catalyst. Linear voltage sweep condition: 5mV s -1 ,1600r min -1 . The catalyst has better SO in the low oxidation range 2 Oxidation performance, but there is a certain gap with Pt / C; after the oxidation potential is higher than 1.186V, it has better SO2 than Pt / C 2 Oxidation properties. Catalyst of the present invention is more suitable for the oxidation potential of 0.9-1.4V scope, test result is as follows figure 1 shown.
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