Modified zeolite catalyst for selective dialkylation of naphthalene

التفاصيل البيبلوغرافية
العنوان: Modified zeolite catalyst for selective dialkylation of naphthalene
المؤلفون: Gary A. Leeke, Joseph Wood, Saeed Hajimirzaee
المصدر: Chemical Engineering Journal. :329-341
بيانات النشر: Elsevier BV, 2012.
سنة النشر: 2012
مصطلحات موضوعية: Thermogravimetric analysis, Chemistry, Thermal desorption spectroscopy, General Chemical Engineering, General Chemistry, Industrial and Manufacturing Engineering, Product distribution, Catalysis, chemistry.chemical_compound, Environmental Chemistry, Organic chemistry, Selectivity, Zeolite, Space velocity, Naphthalene, Nuclear chemistry
الوصف: The dialkylation of naphthalene with isopropanol to produce 2,6-diisopropylnaphthalene (2,6-DIPN) was carried out over HY zeolite. The effects of various reaction conditions, such as pressure, temperature, space velocity, molar ratio of alcohol to naphthalene and time on stream (TOS) on product distribution were studied. HY zeolite was modified by transition metals, such as Fe 3+ , Ni 2+ , Co 2+ and Cu 2+ using wet impregnation method to maximize the selectivity to 2,6-DIPN. The catalysts were characterized by XRF, XRD, TGA, nitrogen adsorption–desorption and Temperature Programmed Desorption (TPD) of t-Butylamine. Under optimum reaction conditions, (50 bar, 220 °C, isopropanol/naphthalene = 4 (mole ratio), WHSV = 18.8 h −1 , TOS 6 h), HY zeolite modified by Fe 3+ was found to give the highest selectivity, by increasing the 2,6/2,7-DIPN ratio from 2.8 to 6.6. The experimental results indicate that the selectivity to 2,6-DIPN is in the order of Fe–HY > Ni–HY > Cu–HY > Co–HY > HY. Naphthalene conversion of 77% was obtained over HY zeolite, while after modification by Fe, Co, Ni and Cu, the conversion was changed to 73%, 76%, 88% and 96%, respectively. TPD result indicates different distribution of weak, medium and strong acid sites in the modified catalysts. TGA analysis of used catalyst samples revealed that a higher amount of PIPN was produced on zeolite modified by Co and Cu. This confirms that PIPN molecules are possible coke precursors, and therefore led to larger amount of coking on the Co–HY and Cu–HY catalysts.
تدمد: 1385-8947
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::20633f7aeba9ebb13b9e498db02678b6Test
https://doi.org/10.1016/j.cej.2012.06.134Test
حقوق: OPEN
رقم الانضمام: edsair.doi...........20633f7aeba9ebb13b9e498db02678b6
قاعدة البيانات: OpenAIRE