Selective C-alkylation of phenol with methanol over catalysts derived from copper-aluminium hydrotalcite-like compounds

• Published in: Applied catalysis. A, General Vol. 145; no. 1; pp. 141 - 153
• Main Authors: Velu, S., Swamy, C.S.
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 08.10.1996
• Subjects: Acid-base properties; Alkylation of phenol; Hydrotalcite; Hydrotalcite; Alkylation of phenol; Acid-base properties
• ISSN: 0926-860X; 1873-3875
• DOI: 10.1016/0926-860X(96)00133-0

Copper aluminium hydrotalcites (CuAl-HT) with a Cu/Al atomic ratio of 2, 3 and 4 (CuAl 2.0-HT, CuAl 3.0-HT, CuAl 4.0-HT) were synthesised by the coprecipitation method using a mixture of NaOH/Na 2CO 3 as precipitant. The pure crystalline hydrotalcite (HT) phase was detected by X-ray diffraction when the copper-aluminium hydrotalcite was prepared without ageing (CuAl 3.0-WAHT). Vapour phase alkylation of phenol with methanol was carried out over CuAl-HT calcined at 450°C/8 h in air (CuAl-CHT). The activity and selectivity of these catalysts were compared with those of magnesium-aluminium calcined hydrotalcites (MgAl 4.0-CHT) from our earlier report. MgAl 4.0-CHT showed higher selectivity for 2,6-xylenol whereas CuAl-CHT was selective for o-cresol. Among the CuAl-CHT studied, CuAl 3.0-CHT showed higher phenol conversion at low temperatures (250–350°C). The catalyst derived from pure copper-aluminium hydrotalcite (CuAl 3.0-WACHT) showed lowest phenol conversion compared to other copper based catalysts obtained from a mixture of HT and malachite phases. The selectivity for o-cresol decreased in the order CuAl 3.0-CHT > CuAl 2.0-CHT > CuAl 3.0-WACHT ≈ CuAl 4.0-CHT > MgAl 4.0-CHT at low phenol conversion levels (15–20%). A suitable reaction pathway for the alkylation of phenol with methanol over these catalysts has been proposed after a careful examination of the reaction sequence. The selective C-alkylation to give o-cresol and 2,6-xylenol over CuAl-CHT could be attributed to the higher acidity of these catalysts as evidenced by the higher cyclohexanol dehydration activity.