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Showing papers on "o-Cresol published in 2002"


Journal ArticleDOI
TL;DR: The ring-retaining products of the OH-initiated degradation of phenol and o -, m -, and p -cresol in the presence of NO x have been investigated and their formation yields determined as mentioned in this paper.

168 citations


Journal ArticleDOI
TL;DR: In this article, the alkylation of phenol with methanol is conducted over Ni 1− x Co x Fe 2 O 4 (x = 0, 0.2, 0., 0.5, 1.8, and 1.0) type systems prepared via low temperature route.
Abstract: The alkylation of phenol with methanol is conducted over Ni 1− x Co x Fe 2 O 4 ( x =0, 0.2, 0.5, 0.8 and 1.0) type systems prepared via low temperature route. Alkylation leads to predominantly ortho methylation of phenol, yielding o -cresol and 2,6-xylenol as the products. Under optimized conditions, the total ortho selectivity was ≥94%, regardless of the catalyst composition. Only traces of anisole is formed and hardly any other xylenol or cresol isomers are detected. Phenol conversion and the individual selectivities for o -cresol and 2,6-xylenol depend strongly on the catalyst composition. Selectivity for o -cresol was maximum for NiFe 2 O 4 (i.e., when x =0), whereas upon progressive substitution of Co 2+ ions for Ni 2+ ions, the 2,6-xylenol selectivity increases with a concomitant decrease in the o -cresol selectivity. Maximum phenol conversion and 2,6-xylenol selectivity (also total ortho selectivity) were observed over CoFe 2 O 4 ( x =1). The activity and selectivity were shown to be strongly dependent on the surface acid–base properties of the system. The influences of surface acidity, cation distribution in the spinel lattice and various reaction parameters are discussed.

74 citations