1, 1, 2, 2, 3, 3, 4-heptafluorocyclopentane as well as preparation method and application thereof
A technology of heptafluorocyclopentane and contact reaction, which is applied to the preparation of halogenated hydrocarbons, preparation of dehalogenation, chemical instruments and methods, etc., to achieve the effect of easy to obtain raw materials, not easy to deposit carbon, and mild reaction conditions
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[0033] S1. Contact the first solution with the carrier to perform impregnation treatment to obtain a catalyst precursor; the first solution is composed of at least Pd, Pt, Ru, Co, Ni, Cu, Bi, Zn, B, P a salt solution of an element;
[0034] S2. performing a reduction reaction on the catalyst precursor and a reducing agent.
[0035] Preferably, in step S1, the conditions of the immersion treatment at least include: a temperature of 20-40° C. and a time of 6-12 hours.
[0036] Preferably, in step S2, the reducing agent is at least one selected from hydrogen, potassium borohydride, and sodium borohydride.
[0037] Preferably, in step S2, the reduction reaction conditions at least include: a temperature of 50-200° C. and a time of 1-15 h.
[0038] Preferably, in step S2, the preparation method of the catalyst A further includes: before performing the reduction treatment, first drying the catalyst precursor.
[0039] Preferably, the drying treatment conditions at least include: ...
preparation example 1
[0067] S1. At 25°C, dissolve 0.83g of palladium chloride in 20mL of hydrochloric acid, and add 100g of AlF 3 , stand still for 12h, and filter to obtain the catalyst precursor;
[0068] S2. At 60°C, reduce all the catalyst precursors obtained above with 17.5 g of 1 wt% sodium borohydride solution for 2 hours to obtain catalyst A1;
[0069] In catalyst A1, the content of active metal element Pd is 0.5wt%, the content of promoter element B is 0.05wt%, and the balance is AlF 3 carrier.
[0070] Preparation example 2
preparation example 2
[0072] S1. At 25°C, add 0.86g of platinum tetrachloride into deionized water, and add 100g of AlF 3 , stand still for 12h, and filter to obtain the catalyst precursor;
[0073] S2. At 80°C, reduce all the catalyst precursors obtained above with 17.5 g of 1 wt% sodium borohydride solution for 2 hours to obtain catalyst A2;
[0074] In catalyst A2, the content of active metal element Pt is 0.5wt%, the content of promoter element B is 0.05wt%, and the balance is AlF 3 carrier.
[0075] Preparation example 3
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