Method for preparing light olefins from methanol using hydrocarbons as part material
A technology for the preparation of low-carbon olefins and methanol, which is applied in the direction of biological raw materials, ethylene production, and hydrocarbon production from oxygen-containing organic compounds. It can solve the problems of increasing energy consumption and reducing the space-time yield of target products, so as to save energy and reduce reaction Thermal effect, effect of reducing dosage
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Embodiment 1
[0049] The preparation of embodiment 1 catalyst
[0050] Mix 30.15g of aluminum isopropoxide with 54.17g of water, add 17.11g of phosphoric acid while stirring, continue stirring, add 9.32g of tetraethyl silicate, and finally add 36.19g of 30% tetraethylammonium hydroxide template, Continue stirring to form a homogeneous gel. The above gel solution was transferred into a stainless steel crystallizer, sealed, and left to stand at a constant temperature of 200°C for 120 hours for crystallization. After the crystallization is completed, the product is cooled rapidly, the mother liquor is poured out, the precipitate is separated by centrifugation, and washed several times with pure water until the pH value of the solution is 8-9, and then the obtained crystal is dried at 115°C for 3 hours, 550 The templating agent was removed by calcining at ℃ for 5 hours to obtain SAPO-34 molecular sieve. The obtained SAPO-34 molecular sieve is directly compressed into tablets, and the particle...
Embodiment 2
[0052] On the continuous flow fixed-bed reaction device, 3ml of the catalyst prepared in Example 1 was loaded. Under normal pressure, air flow, flow rate 50ml / min, calcinate the catalyst at 500°C for 2 hours, then switch to N 2 Purge for 0.5 hours. to N 2 It is the carrier gas, the flow rate is 50ml / min, methanol and carbon tetraolefins are used as raw materials, the molar ratio is, methanol: carbon tetraolefins = 1:0.167, and the mass space velocity is 3h -1 , the reaction temperature is 380°C. Table 1 is the raw material composition of carbon tetraolefins. Table 2 shows the results of the methanol-to-olefins reaction when carbon tetraolefins are used as part of the feed.
Embodiment 3
[0060] Using the same catalyst, raw materials, and experimental conditions as in Example 2, the experimental results when the reaction temperatures were 350° C. and 480° C. are shown in Table 3.
[0061] Table 3 The reaction results of C4-olefins as co-feed methanol to olefins
[0062] temperature, ℃ 350 480 Product composition wt% wt% methanol + dimethyl ether 0 0 C1+C2+C3 3.21 8.62 C2= 21.58 24.44 C3= 32.16 35.21 C4 24.82 16.17 C5+ hydrocarbons 16.93 5.36 Aromatics 0.24 1.56 COx 1.06 8.64
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