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Please use this identifier to cite or link to this item: http://hdl.handle.net/11375/13729
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dc.contributor.advisorAnderson, R.B.en_US
dc.contributor.authorNicolau, Ioanen_US
dc.date.accessioned2014-06-18T17:05:01Z-
dc.date.available2014-06-18T17:05:01Z-
dc.date.created2009-08-21en_US
dc.date.issued1975-09en_US
dc.identifier.otheropendissertations/856en_US
dc.identifier.other1742en_US
dc.identifier.other960992en_US
dc.identifier.urihttp://hdl.handle.net/11375/13729-
dc.description.abstract<p>The amount and nature of hydrogen in Raney nickel catalysts were determined by various methods: thermal desorption in a volumetric apparatus, temperature-programmed desorption using argon as a carrier gas and techniques similar to those of Amenomiya and Cvetanovic, hydrogen-deuterium exchange, dissolution in acids and other methods. Most of the hydrogen removed in thermal desorption can not be re-adsorbed. Desorption was generally exothermic and each type of sample had a characteristic TPD spectrum. Water vapor, introduced over the catalyst, increased the hydrogen evolution sizeably and this process was also exothermic. Under these conditions water will not oxidize bulk nickel. Present results suggest that the reaction of residual aluminum and water is an important source of hydrogen evolved on heating Raney nickel, but part of the hydrogen is held interstitially.</p>en_US
dc.subjectChemistryen_US
dc.subjectChemistryen_US
dc.titleThe Nature of Hydrogen in Raney Nickel Catalystsen_US
dc.typethesisen_US
dc.contributor.departmentChemistryen_US
dc.description.degreeDoctor of Philosophy (PhD)en_US
Appears in Collections:Open Access Dissertations and Theses

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