Platinum-cobalt dual-metal catalyst with room-temperature benzene hydrogenation activity and preparation method thereof
A bimetallic catalyst and catalyst technology, applied in the direction of metal/metal oxide/metal hydroxide catalyst, hydrogenation hydrocarbon production, chemical instruments and methods, etc., can solve the problems of no patents and literature reports, etc., and achieve high room temperature heating Effects of hydrogen efficiency, energy saving, and process simplification
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Embodiment 1
[0028] Embodiment 1, preparation and activity evaluation of catalyst
[0029] 1. Preparation of catalyst
[0030] 1. Preparation of catalyst precursor
[0031] 0.07g Pt(NH 3 ) 4 (NO 3 ) 2 and 1.5g Co(NO 3 ) 2 ·6H 2 O was dissolved in 100 mL of deionized water, 2.9 g of activated carbon was added, stirred magnetically for 2 h, evaporated to dryness in a water bath at 95 °C, and then dried in an oven at 110 °C for 12 h.
[0032] 2. Preparation of catalyst
[0033] Put 120 mg of the catalyst precursor prepared in step 1 into a U-shaped quartz tube, activate in hydrogen-nitrogen mixed gas at 350° C. for 1 h, and flow both hydrogen and nitrogen at 20 mL / min.
[0034] 2. Catalyst performance evaluation
[0035] 1. Determination of metal specific surface area and CO chemical adsorption capacity of catalyst
[0036] The metal specific surface area and CO chemisorption capacity of the catalyst prepared in step 1 were measured, and the results are shown in Table 1.
[0037] ...
Embodiment 2
[0040] Embodiment 2, catalyst preparation and activity evaluation
[0041] 1. Preparation of catalyst
[0042] 1. Catalyst precursor preparation
[0043]0.07g Pt(NH 3 ) 4 (NO 3 ) 2 and 1.5g Co(NO 3 ) 2 ·6H 2 O was dissolved in 100 mL of deionized water, 2.9 g of activated carbon was added, stirred magnetically for 2 h, evaporated to dryness in a water bath at 95 °C, and then dried in an oven at 110 °C for 12 h.
[0044] 2. Catalyst activation
[0045] Put 100 mg of the catalyst precursor prepared in step 1 into a U-shaped quartz tube, activate in a hydrogen-nitrogen mixed gas at 500°C for 1 h, and flow both hydrogen and nitrogen at 20 mL / min.
[0046] 2. Catalyst performance evaluation
[0047] 1. Determination of metal specific surface area and CO chemical adsorption capacity of catalyst
[0048] The metal specific surface area and CO chemisorption capacity of the catalyst prepared in step 1 were measured, and the results are shown in Table 1.
[0049] 2. Benzene ...
Embodiment 3
[0052] Embodiment 3, catalyst preparation and activity evaluation
[0053] 1. Preparation of catalyst
[0054] 1. Preparation of catalyst precursor
[0055] 0.07g Pt(NH 3 ) 4 (NO 3 ) 2 and 1.5g Co(NO 3 ) 2 ·6H 2 O was dissolved in 100 mL of deionized water, 2.9 g of activated carbon was added, stirred magnetically for 2 h, evaporated to dryness in a water bath at 95 °C, and then dried in an oven at 110 °C for 12 h.
[0056] 2. Catalyst activation
[0057] 120 mg of the catalyst precursor prepared in Step 1 was put into a U-shaped quartz tube, activated in nitrogen at 500°C for 1 h, and the nitrogen flow rate was 50 mL / min.
[0058] 2. Catalyst performance evaluation
[0059] After step 1 is completed, a reaction gas is introduced into the U-shaped quartz tube, the reaction gas is a hydrogen-nitrogen mixture, and the flow rates are 10 mL / min and 40 mL / min, respectively. Benzene was injected with a micropump at a flow rate of 0.5mL / h, and was brought into the catalyst...
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