Dehydration and dehydrogenation of 2-octanol by thorium oxide
References (20)
- et al.
Advan. Catal.
(1966) - et al.
J. Catal.
(1964) Angew. Chem. Int. Ed.
(1968)Ann. Chim. Phys.
(1910)- et al.
Kinet. Katal.
(1961) Vestn. Mosk. Univ. #3
(1951)- et al.
J. Amer. Chem. Soc.
(1927) - et al.
J. Amer. Chem. Soc.
(1963)et al.J. Org. Chem.
(1967)
There are more references available in the full text version of this article.
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2020, Applied Catalysis A: GeneralCitation Excerpt :The selectivity of dehydration is often hampered by many side products originating from reactions such as dehydrogenation, dehydrocyclization, and dimerization. In general, preparation and pretreatment conditions of metal oxides have played a significant role in modifying the activity and selectivity of dehydration and other acid-catalyzed reactions [6]. Alumina and zirconia are considered to be highly selective dehydration catalysts, but they can still produce a wide range of products if subjected to different pretreatment conditions [7–9].
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