High-dispersion dual-functional catalyst for hydrogenating and deoxidizing phenol and preparation method of catalyst
A dual-function catalyst and hydrodeoxygenation technology, which is applied in hydrogenation preparation, molecular sieve catalyst, carbon-based compound preparation, etc., can solve problems such as uneven distribution of functional groups, irregular material channels, uneven metal dispersion, etc., and achieve uniform distribution of functional groups , low cost, uniform distribution of active components
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Embodiment 1
[0032] 4.00 g (0.69 mmol) of Pluronic P123 was dissolved in 150 mL of 0.03 mol / L HCl solution at room temperature, heated to 40 °C with stirring, and then tetraethylorthosilicate TEOS (9.00 g, 43.20 mmol) was added. TEOS was prehydrolyzed for 2 hours and then 143 μL (0.7652 mmol) of mercaptopropyltrimethoxysilane (MPTMS) and 0.0299 g (0.1530 mmol) of chloroplatinic acid (H 2 PtCl 60.01 g Pt / mL solution) and 1.2605 g (6.171 mmol) of aluminum isopropoxide (AIP). The resulting mixture was stirred at 40 °C for 24 h and then left to age at 100 °C for 24 h. The obtained solid material was filtered, dried at 100 °C for 8 h, and finally calcined in an air atmosphere in a muffle furnace, heated to 500 °C at a heating rate of 2 °C / min, then kept at 500 °C for 6 h, and cooled to room temperature to obtain a solid. Metal active and acidic bifunctional catalyst 1%Pt-(SH) / Al-SBA-15(7).
[0033] The activity evaluation reaction is to dissolve 1.1764 g (0.0125 mol) phenol in 25.0 mL of dic...
Embodiment 2
[0035] The catalyst was prepared according to the method of Example 1 to obtain a 1% Pt-(SH) / Al-SBA-15(7) catalyst. The other activity evaluation conditions were the same as in Example 1 except for the solvent. Take water, ethanol and toluene as solvent to do three groups of reactions respectively, and the results are shown in Table 1.
Embodiment 3
[0037] The catalyst was prepared according to the method of Example 1 to obtain a 1% Pt-(SH) / Al-SBA-15(7) catalyst. Three groups of reactions were performed under the conditions of reaction temperatures of 30°C, 50°C and 100°C, respectively, and other activity evaluation conditions were the same as those in Example 1 except for the reaction temperature conditions. The results are shown in Table 2 (for the convenience of comparison, the reaction at 180° C. is also listed in Table 2).
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