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Titlebook: Catalytic Activation and Functionalisation of Light Alkanes; Advances and Challen Eric G. Derouane,Jerzy Haber,Michel Guisnet Book 1998 Spr

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书目名称Catalytic Activation and Functionalisation of Light Alkanes
副标题Advances and Challen
编辑Eric G. Derouane,Jerzy Haber,Michel Guisnet
视频video
丛书名称NATO Science Partnership Subseries: 3
图书封面Titlebook: Catalytic Activation and Functionalisation of Light Alkanes; Advances and Challen Eric G. Derouane,Jerzy Haber,Michel Guisnet Book 1998 Spr
描述Light alkanes tend to be resistant to many forms of activation.The horizontal approach of the present book covers homogeneous,heterogeneous and biological catalysis, thus allowing readers to gainan awareness of progress and ideas in research areas different fromtheir own. The book contains both general chapters, giving an overviewof the subject, and specialised contributions that deal with thedetails and state of the art. A specialist report is also includedwhich gives a critical insight into current progress and discussesfuture prospects and major challenges. ..Audience:. Newcomers and senior researchers in the field ofalkane activation. The mixed theoretical and practical approach willbe of interest to researchers and industrialists alike.
出版日期Book 1998
关键词Chlor; catalysis; chemistry; hydrogen; methanol; zeolites
版次1
doihttps://doi.org/10.1007/978-94-017-0982-8
isbn_softcover978-90-481-4999-5
isbn_ebook978-94-017-0982-8Series ISSN 1388-6576
issn_series 1388-6576
copyrightSpringer Science+Business Media Dordrecht 1998
The information of publication is updating

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The Concepts of ‘Civilisation’ and ‘Culture’d tungsten carbides possess a . surface that catalyzes both dehydrogenation and carbenium ion reactions typically occurring on reforming catalysts [3]. These findings are not unique to tungsten carbides and depend on the preparation of materials.
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The Effect of Acid Sites in Skeletal Isomerization of N-Butenes over Ferrierites and Coalpo-11 at least 48 hrs. This is a result, besides very narrow channels, of cooperative effect of weakly acidic both P-OH groups and Co.  Lewis sites. When P-OH groups were completely removed by calcination, skeletal isomerization selectively proceeds only on Co. sites.
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Oxidative Dehydrogenation of Propane on Large-Pore Zeolitesd by the faujasite matrix significantly increase the selectivity to propene [2]. Preliminary results on zeolite Beta modified with Ga- and B-species [3] have also shown that this structure possesses promising activity and selectivity in the oxidative dehydrogenation (ODH) of propane.
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Oxidative Coupling of Methane over Sodium-Manganese Catalysts in the Presence of HCIcts and on the time-on-stream has been studied. Addition of HC1 into initial methane-oxygen mixture can increase selectivity to C. and decrease selectivity to carbon oxide’s formation. In the presence of HC1 the time-onstream increases to 35–40 h. On the basis of these results the mechanism of OCM reaction is also discussed.
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