Alkylation of naphthalene with isopropanol over dealuminium USY catalysts
Wenliang Wu
Abstract
Wenliang Wu
Abstract
Highly active catalysts were prepared by dealuminumed USY with water vapour,ammonium nitrate aqueous solution and 12-tungstophosphoric acid(PW).The properties of the catalysts were identified by X-ray diffraction(XRD),N2 adsorption and desorption,pyridine infrared spectroscopy(Py-IR) techniques.The results showed that USY kept large relative crystallinity,high relative crystallinity and large L acid amount when dealuminum was appropriately completed.Using USY dealuminum treated with water vapour as the catalyst,conversion of naphthalene was 92.3%,selectivity of DIPN,β-IPN and β,β′-DIPN reached 45.9%,94.4%,and 85.3%. The suitable reaction conditions were as follows: calcination temperature was 550 ℃,reaction temperature was 160 ℃ and reaction balanced time was 150 min.After reacting 4 times,the conversion rate of naphthalene kept above 73% and selectivity of β,β′-DIPN preserved without obviously declined.
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Highly active catalysts were prepared by dealuminumed USY with water vapour,ammonium nitrate aqueous solution and 12-tungstophosphoric acid(PW).The properties of the catalysts were identified by X-ray diffraction(XRD),N2 adsorption and desorption,pyridine infrared spectroscopy(Py-IR) techniques.The results showed that USY kept large relative crystallinity,high relative crystallinity and large L acid amount when dealuminum was appropriately completed.Using USY dealuminum treated with water vapour as the catalyst,conversion of naphthalene was 92.3%,selectivity of DIPN,β-IPN and β,β′-DIPN reached 45.9%,94.4%,and 85.3%. The suitable reaction conditions were as follows: calcination temperature was 550 ℃,reaction temperature was 160 ℃ and reaction balanced time was 150 min.After reacting 4 times,the conversion rate of naphthalene kept above 73% and selectivity of β,β′-DIPN preserved without obviously declined.
Key concepts: Naphthalene, Catalysis, Crystallinity, Calcination, Chemistry, Selectivity, Inorganic chemistry, Pyridine