Catalyst for producing tetrafluoromethane by gas-phase fluorination and preparation method thereof
A tetrafluoromethane, gas-phase fluorination technology, applied in the direction of physical/chemical process catalysts, chemical instruments and methods, metal/metal oxide/metal hydroxide catalysts, etc., can solve the problems of low operating temperature, poor activity, and stability No high problems, to achieve the effect of low temperature, high stability, high catalytic activity or selectivity
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Embodiment 1
[0032] First, weigh Cr according to the molar ratio between Cr and Al is 1:4 2 o 3 and Al(OH) 3 , mix evenly with an appropriate amount of water, add a certain amount of ammonia water until the precipitation is complete, then separate and wash until the filtrate is neutral, and then dry the precipitate at 70°C. After the dried precipitate was molded, it was heated at 300°C and N 2 Calcined in the atmosphere for 48 hours to obtain a fluorinated catalyst precursor. The fluorination catalyst precursor was treated with HF at 250° C. for 48 hours to obtain a fluorination catalyst. Its reactivity or selectivity are shown in Table 1, Table 2, Table 3, Table 4.
Embodiment 2
[0034] First, weigh Cr(OH) according to the molar ratio between Cr and Al of 1:19 3 and Al(NO3 ) 3 , mix well with an appropriate amount of water, add a certain amount of Na 2 CO 3 After the precipitation is complete, it is separated and washed until the filtrate is neutral, and then the precipitate is dried at 120°C. After the dried precipitate was molded, it was heated at 600°C and N 2 Calcined in the atmosphere for 24 hours to obtain a fluorinated catalyst precursor. The fluorination catalyst precursor was treated with HF at 400° C. for 30 hours to obtain a fluorination catalyst. Its reactivity or selectivity are shown in Table 1, Table 2, Table 3, Table 4.
Embodiment 3
[0036] First, weigh CrCl according to the molar ratio between Cr and Al of 1:3 3 and Al 2 o 3 , mix evenly with an appropriate amount of water, add a certain amount of KOH until the precipitation is complete, then separate and wash until the filtrate is neutral, and then dry the precipitate at 90°C. The dried precipitate is shaped and calcined at 400° C. in an air atmosphere for 36 hours to obtain a fluorination catalyst precursor. The fluorination catalyst precursor was treated with HF at 350° C. for 35 hours to obtain a fluorination catalyst. Its reactivity or selectivity are shown in Table 1, Table 2, Table 3, Table 4.
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