摘要
Titanium silicalite-1 （TS-1） has been hydrothermally synthesized with tetrapropylammonium hydroxide （TPAOH） as the template in the presence of various amounts of Na＋, characterized by inductively coupled plasma, X-ray diffraction, scanning electron microscope, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy and ultro-violet-visible spectroscopy and studied in cyclohexanone ammoximation. The characterization results show that with the increase of Na＋ concentration in the synthesis, both the crystal sizes of TS- land extra framework Ti increase but framework Ti decreases. The addition of Na＋ below 3 mol-% of TPAOH in the synthesis does not influence the catalytic properties with above 98% conversion of cyclohexanone and 99.5% selectivity to cyclohexanone oxime. However, at the concentrations of Na＋≥3mol-% of TPAOH in the synthesis, the catalysts are deactivated faster with the increase of Na＋ addition, which can be attributed to more high molecular weight byproducts deposited in the large TS-1 particles and the loss of the frame-work titanium. The results of this work are of great importance for the industry.
Titanium silicalite-1 （TS-1） has been hydrothermally synthesized with tetrapropylammonium hydroxide （TPAOH） as the template in the presence of various amounts of Na＋, characterized by inductively coupled plasma, X-ray diffraction, scanning electron microscope, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy and ultro-violet-visible spectroscopy and studied in cyclohexanone ammoximation. The characterization results show that with the increase of Na＋ concentration in the synthesis, both the crystal sizes of TS- land extra framework Ti increase but framework Ti decreases. The addition of Na＋ below 3 mol-% of TPAOH in the synthesis does not influence the catalytic properties with above 98% conversion of cyclohexanone and 99.5% selectivity to cyclohexanone oxime. However, at the concentrations of Na＋≥3mol-% of TPAOH in the synthesis, the catalysts are deactivated faster with the increase of Na＋ addition, which can be attributed to more high molecular weight byproducts deposited in the large TS-1 particles and the loss of the frame-work titanium. The results of this work are of great importance for the industry.
基金
Acknowledgements This work has been supported by the National Natural Science Foundation of China （Grant No. 21276183） and Program of Introducing Talents of Discipline to Universities （No. B06006）.
