Methane conversion process
A methane conversion technology, applied in the integrated field of production of liquefied natural gas and/or pipeline gas, can solve the problems of high investment and energy costs and low efficiency of synthesis gas
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Embodiment 1
[0119] By blending ZSM-5 and MoO with a molar ratio of silica to alumina of 25:1 3 , and then the resulting blend was calcined at 500 °C for 5 h in air to prepare a 2.7 wt% Mo / ZSM-5 catalyst.
[0120] The catalyst was then heated to 800 °C in helium, after which it was sufficient to obtain 4 hr -1 The 95% methane / 5% argon feedstock supplied at the WHSV rate replaces helium. Benzene production was measured over a 60-minute continuous on-time period, and at Figure 4 The results are shown in .
[0121] Repeat the above experiment, but use the volume containing 100ppm H 2 S 95% methane / 5% argon feedstock. Benzene production was again measured over the 60 min continuous on-time period, and at Figure 4 The results are shown in . Surprisingly, it was found that the presence of 100 ppm by volume of H2S had no significant effect on the yield of benzene.
Embodiment 2
[0123] Repeat the procedure of Example 1, but before heating to 800°C in helium, pass through 15% CH 4 / 85%H 2 The mixture was heated to 650 °C to pre-carburize the 2.7wt% Mo / ZSM-5 catalyst. In one test, the precarburized mixture also contained 100 ppm volume H 2 S, while in another test, the precarburized mixture contained only CH 4 and H 2 . Figure 5 The results are shown in , and show that when the H 2 MoO in the presence of S 3 During precarburization, the yield of benzene decreased slightly.
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