A kind of preparation method of m-xylylenediamine
A technology for m-xylylenediamine and m-xylylenediamine preparation, which is applied in the field of m-xylylenediamine preparation, can solve the problems of reducing catalyst acidity and affecting economy, and achieve the effect of promoting dispersion
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Embodiment 1
[0022] Weigh 29.7g Ni(NO 3 ) 2 ·6H 2 O, 19.1g Mg(NO 3 ) 2 ·6H 2 O and 7.4g Al(NO 3 ) 3 9H 2 Dissolve O in water to make a 100ml solution; take another 24.1g Na 2 CO 3 Dissolve in water to make 100ml solution. Add the above two solutions dropwise to 200ml of distilled water at the same time under stirring to form a green precipitate. After washing the precipitate with distilled water, add 200ml of n-butanol, evaporate to dryness in a water bath, dry in a 393K oven, and then press into tablets. Crush and sieve 20-40 mesh, reduce the catalyst precursor particles in flowing hydrogen at 723K for 2 hours, hydrogen GSVH=1000h -1 , then at room temperature with 0.5% O 2 / N 2 The mixed gas is passivated to obtain catalyst A.
Embodiment 2
[0024] Weigh 29.7g Ni(NO 3 ) 2 ·6H 2 O, 22.3g Mg(NO 3 ) 2 ·6H 2 O and 3.7g Al(NO 3 ) 3 9H 2 Dissolve O in water to make a 100ml solution; take another 23.8g Na 2 CO 3 Dissolve in water to make 100ml solution. Add the above two solutions dropwise to 200ml of distilled water at the same time under stirring to form a green precipitate. After washing the precipitate with distilled water, add 200ml of n-butanol, evaporate to dryness in a water bath, dry in a 393K oven, and then press into tablets. Crush and sieve 20-40 mesh, reduce the catalyst precursor particles in flowing hydrogen at 723K for 2 hours, hydrogen GSVH=1000h -1 , then at room temperature with 0.5% O 2 / N 2 The mixed gas is passivated to obtain catalyst B.
Embodiment 3
[0026] Weigh 29.7g Ni(NO 3 ) 2 ·6H 2 O, 23.9g Mg(NO 3 ) 2 ·6H 2 O and 1.8gAl(NO 3 ) 3 9H 2 Dissolve O in water to make a 100ml solution; take another 23.6g Na 2 CO 3 Dissolve in water to make 100ml solution. Add the above two solutions dropwise to 200ml of distilled water at the same time under stirring to form a green precipitate. After washing the precipitate with distilled water, add 200ml of n-butanol, evaporate to dryness in a water bath, dry in a 393K oven, and then press into tablets. Crush and sieve 20-40 mesh, reduce the catalyst precursor particles in flowing hydrogen at 723K for 2 hours, hydrogen GSVH=1000h -1 , then at room temperature with 0.5% O 2 / N 2 The mixed gas is passivated to obtain catalyst C.
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