Formaldehyde degradation catalyst and preparation method thereof
A formaldehyde degradation and catalyst technology, applied in chemical instruments and methods, physical/chemical process catalysts, separation methods, etc., can solve problems that need to be further improved, to avoid secondary pollutants, strengthen water resistance, and specific surface area big effect
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[0030] A kind of preparation method of formaldehyde degradation catalyst, it comprises steps:
[0031] S100 Prepare a porous matrix, dissolve 2,2'-bipyridine and bis-(1,5-cyclooctadiene) nickel in dry N,N-dimethylformamide to obtain a mixed solution, add 1 at intervals, 5-Cyclooctadiene and 2,4,6-tri-p-bromophenyl-[1,3,5]triazine were reacted in the mixed solution to obtain a dark purple mixture. After the mixture was cooled, concentrated hydrochloric acid was added, filtered, Washing, standing and supercritical extraction to prepare covalent organic porous polymer COP-4; and
[0032] S200 supergravity loading active components, adding the porous matrix to the dimethylformamide solution containing gold precursor and platinum precursor, placing it in a supergravity packed bed and treating it under the condition of 100-250g supergravity 2 ~5 hours to prepare a catalyst sample; and
[0033] S300 calcination combines the active component and the porous substrate. The catalyst sa...
Embodiment 1
[0051] First, 16g of 2,2'-bipyridine and 28g of bis-(1,5-cyclooctadiene)nickel were added to 500mL of dry N,N-dimethylformamide solution and stirred rapidly at a temperature of 80°C until the sample is completely dissolved. Then 12.5 mL of 1,5-cyclooctadiene was added to the above mixture and stirred well. Then 11 g of 2,4,6-tri-p-bromophenyl-[1,3,5]triazine was added to the above mixed solution, and reacted at 105° C. for 12 h to finally obtain a dark purple mixture. After the mixture was cooled down, concentrated hydrochloric acid was added thereto until its color changed to transparent green. The mixture was then filtered and washed with chloroform, tetrahydrofuran and water, respectively. The samples obtained after filtration and washing were placed in absolute ethanol and left to stand for 3 days. The samples were then transferred to supercritical CO 2 In the extraction device, inject CO at a rate of 50-100mL / min 2 , the pressure was maintained at 1300psi, then the t...
Embodiment 2
[0055] The preparation process of COP-4 is the same as that of Example 1, 5.0gCOP-4 is added in the 200mLDMF solution containing 0.80mmol / L chloroauric acid, then it is placed in the supergravity packed bed and treated under the supergravity condition of 250g for 2h . Subsequently, the obtained samples were dried at 120°C for 6 h, and placed in N at 400°C. 2 Calcination treatment under atmosphere for 4h, followed by H at 400°C 2 Reduction treatment under atmosphere for 3h. Finally, the loaded amount of Au element was determined to be 0.3wt% by ICP-MS. Finally, after tableting, crushing and sieving, a catalyst of 40 mesh to 60 mesh was taken for activity evaluation.
[0056] The experimental results show that at room temperature of 25°C, the degradation rate of formaldehyde is maintained at about 85.6%. 2 The selectivity is maintained at 90%, and some CO is generated.
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