Method for removing trace olefin from aromatic hydrocarbon
An aromatics and removal technology, applied in the direction of chemical change purification/separation, organic chemistry, etc., can solve the problems of poor catalyst activity stability, large internal diffusion resistance, large catalyst coking deactivation rate, etc. Simple process, avoids reaction and regenerates the effect of frequent switching operations
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[0031] Example 1:
[0032] Synthetic B-AlPO 4 -5 / Hβ core-shell composite molecular sieve catalyst, denoted as CAT-1.
[0033] 80 grams of Hβ microporous molecular sieve powder was used as the core, and 500 grams of deionized water was stirred and mixed for 1.0 hour to obtain a mixture A. Follow Al 2 O 3 : P 2 O 5 : B 2 O 3 : OXAA: H 2 O: ETHA: The molar ratio of TEA raw materials is 1:0.432:0.191:0.304:25.368:2.352:0.756, 40 grams of monohydrate alumina, and the corresponding amount of phosphoric acid (H 3 PO 4 , Purity 85wt%), boric acid, oxalic acid (OXAA), deionized water, anhydrous ethanol (ETHA) and triethylamine (TEA) mixture was stirred and mixed for 0.5 hours to prepare mixture B. Add mixture A to mixture B, continue to stir and mix for 4.5 hours, place it in a stainless steel reactor, crystallize at 150°C for 3 days; then filter, wash, dry, and roast at 550°C for 5 hours to remove the template to obtain the inner core Hβ Microporous molecular sieve mass accounts for 34.8%...
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[0034] Example 2:
[0035] Synthetic Mg-AlPO 4 -5 / Hβ composite molecular sieve catalyst, denoted as CAT-2.
[0036] Using 2.0 g of Hβ microporous molecular sieve powder as the core, stirring and mixing with 20 g of deionized water for 1.0 hour, to obtain a mixture A. Follow Al 2 O 3 : P 2 O 5 : MgO: OXAA: H 2 O: ETHA: TPA raw material molar ratio 1:0.541:0.227:0.061:27.482:2.353:0.758, 40 grams of alumina monohydrate, and the corresponding amount of phosphoric acid (H 3 PO 4 , 85wt%), magnesium acetate, oxalic acid (OXAA), deionized water, ethanol (ETHA), tri-n-propylamine (TPA) mixture was stirred and mixed for 0.5 hours to prepare mixture B. Add mixture A to mixture B, continue to stir and mix for 4.5 hours, place it in a stainless steel reactor, crystallize at 150°C for 3 days; then filter, wash, dry, and roast at 550°C for 5 hours to remove the template to obtain the inner core Hβ Microporous molecular sieve mass accounts for 1.3% Mg-AlPO 4 -5 / Hβ core-shell composite molecular...
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[0037] Examples 3-7:
[0038] Using HZSM-5 molecular sieve, HY molecular sieve, HUSY molecular sieve, HMOR molecular sieve, HMCM-22 molecular sieve as the inner microporous molecular sieve, after hydrothermal synthesis, B-AlPO with the inner microporous molecular sieve mass accounted for 34.8% 4 -5 / microporous molecular sieve core-shell composite molecular sieve catalyst, other operations are the same as in Example 1, and the results are listed in Table 1.
[0039] Table 1
[0040]
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