Citation: MO Zhou-Sheng, QIN Yu-Cai, ZHANG Xiao-Tong, DUAN Lin-Hai, SONG Li-Juan. Influencing Mechanism of Cyclohexene on Thiophene Adsorption over CuY Zeolites[J]. Acta Physico-Chimica Sinica, ;2017, 33(6): 1236-1241. doi: 10.3866/PKU.WHXB201703281
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A CuY zeolite prepared by liquid phase ion exchange was characterized by X-ray photoelectron spectroscopy, pyridine in situ Fourier transform infrared (in situ FTIR) spectroscopy, and ammonia temperature programmed desorption. The effect of cyclohexene on the adsorption of thiophene over the prepared CuY zeolite was explored by in situ FTIR. In particular, the role of the zeolite's Brönsted acidity was investigated in the adsorption process. The results show that the percentage of Cu+ on the surface of the CuY zeolite can reach 77%. The surface acidity of the CuY zeolite mainly comprises medium and strong Brönsted acidity and Lewis acidity. According to the adsorption results, cyclohexene negatively influences thiophene adsorption on the Brönsted or Lewis acid sites in CuY by competitive adsorption. Although polymerization of thiophene and cyclohexene can occur easily on the HY or REY zeolites, the presence of Brönsted acids in the CuY zeolite was not sufficient to polymerize either thiophene or cyclohexene. This difference may be caused by an anti-synergistic effect between the Cu ions of the CuY zeolite and neighboring Brönsted acid sites, the result of which inhibits the polymerization of adsorbed thiophene and cyclohexene.
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