The Effect of Redox Treatment on the Structural, Adsorptive, and Catalytic Properties of Raney Nickel
The effect on Raney nickel catalyst of annealing in hydrogen, and of mild oxidation and subsequent reduction have been studied. The properties investigated are the structure, hydrogen adsorption, and activity for nitrobenzene and potassium maleate liquid-phase hydrogenation. Characterization involve...
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Veröffentlicht in: | Journal of catalysis 1993-06, Vol.141 (2), p.688-699 |
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creator | Mikhailenko, S.D. Khodareva, T.A. Leongardt, E.V. Lyashenko, A.I. Fasman, A.B. |
description | The effect on Raney nickel catalyst of annealing in hydrogen, and of mild oxidation and subsequent reduction have been studied. The properties investigated are the structure, hydrogen adsorption, and activity for nitrobenzene and potassium maleate liquid-phase hydrogenation. Characterization involved X-ray line broadening, adsorption, and capillary condensation of Ar, XPS, and thermoprogrammed reduction. Thermodesorption studies indicate two forms of adsorbed hydrogen, one of which is a weakly bound molecular form and does not depend on treatment, while the other is strongly bound atomic hydrogen whose amount decreases with increase in the annealing temperature. Annealing in hydrogen at T ≥ 200°C causes sintering of the catalysts and a decrease in their activity. Mild oxidation leads to formation of a protective film from nonstoichiometric nickel-oxygen compounds on the Raney Ni surface, preventing it from deep oxidation in the air. A passivated catalyst can be reactivated by heating at 100-300°C in hydrogen, after which the activity for hydrogenation is on par with that of newly prepared catalyst. |
doi_str_mv | 10.1006/jcat.1993.1173 |
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The properties investigated are the structure, hydrogen adsorption, and activity for nitrobenzene and potassium maleate liquid-phase hydrogenation. Characterization involved X-ray line broadening, adsorption, and capillary condensation of Ar, XPS, and thermoprogrammed reduction. Thermodesorption studies indicate two forms of adsorbed hydrogen, one of which is a weakly bound molecular form and does not depend on treatment, while the other is strongly bound atomic hydrogen whose amount decreases with increase in the annealing temperature. Annealing in hydrogen at T ≥ 200°C causes sintering of the catalysts and a decrease in their activity. Mild oxidation leads to formation of a protective film from nonstoichiometric nickel-oxygen compounds on the Raney Ni surface, preventing it from deep oxidation in the air. A passivated catalyst can be reactivated by heating at 100-300°C in hydrogen, after which the activity for hydrogenation is on par with that of newly prepared catalyst.</description><identifier>ISSN: 0021-9517</identifier><identifier>EISSN: 1090-2694</identifier><identifier>DOI: 10.1006/jcat.1993.1173</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>400201 - Chemical & Physicochemical Properties ; ADSORPTION ; ANNEALING ; CARBOXYLIC ACIDS ; CATALYSIS ; CATALYSTS ; CATALYTIC EFFECTS ; CHEMICAL REACTIONS ; CHEMISORPTION ; DICARBOXYLIC ACIDS ; ELECTRON SPECTROSCOPY ; ELEMENTS ; HEAT TREATMENTS ; HETEROGENEOUS CATALYSIS ; HYDROGEN ; HYDROGENATION ; INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY ; MALEIC ACID ; METALS ; NICKEL ; NITRO COMPOUNDS ; NITROBENZENE ; NONMETALS ; ORGANIC ACIDS ; ORGANIC COMPOUNDS ; ORGANIC NITROGEN COMPOUNDS ; OXIDATION ; PHOTOELECTRON SPECTROSCOPY ; REDUCTION ; SEPARATION PROCESSES ; SORPTION ; SORPTIVE PROPERTIES ; SPECTROSCOPY ; STRUCTURAL CHEMICAL ANALYSIS ; SURFACE PROPERTIES ; TEMPERATURE DEPENDENCE ; TEMPERATURE RANGE ; TEMPERATURE RANGE 0400-1000 K ; TRANSITION ELEMENTS ; X-RAY SPECTROSCOPY</subject><ispartof>Journal of catalysis, 1993-06, Vol.141 (2), p.688-699</ispartof><rights>1993 Academic Press</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c349t-1deedc8117466408e87fe79d5571ecf98d97169580496ad1a8249f92b130fce03</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1006/jcat.1993.1173$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.osti.gov/biblio/6216447$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Mikhailenko, S.D.</creatorcontrib><creatorcontrib>Khodareva, T.A.</creatorcontrib><creatorcontrib>Leongardt, E.V.</creatorcontrib><creatorcontrib>Lyashenko, A.I.</creatorcontrib><creatorcontrib>Fasman, A.B.</creatorcontrib><title>The Effect of Redox Treatment on the Structural, Adsorptive, and Catalytic Properties of Raney Nickel</title><title>Journal of catalysis</title><description>The effect on Raney nickel catalyst of annealing in hydrogen, and of mild oxidation and subsequent reduction have been studied. The properties investigated are the structure, hydrogen adsorption, and activity for nitrobenzene and potassium maleate liquid-phase hydrogenation. Characterization involved X-ray line broadening, adsorption, and capillary condensation of Ar, XPS, and thermoprogrammed reduction. Thermodesorption studies indicate two forms of adsorbed hydrogen, one of which is a weakly bound molecular form and does not depend on treatment, while the other is strongly bound atomic hydrogen whose amount decreases with increase in the annealing temperature. Annealing in hydrogen at T ≥ 200°C causes sintering of the catalysts and a decrease in their activity. Mild oxidation leads to formation of a protective film from nonstoichiometric nickel-oxygen compounds on the Raney Ni surface, preventing it from deep oxidation in the air. A passivated catalyst can be reactivated by heating at 100-300°C in hydrogen, after which the activity for hydrogenation is on par with that of newly prepared catalyst.</description><subject>400201 - Chemical & Physicochemical Properties</subject><subject>ADSORPTION</subject><subject>ANNEALING</subject><subject>CARBOXYLIC ACIDS</subject><subject>CATALYSIS</subject><subject>CATALYSTS</subject><subject>CATALYTIC EFFECTS</subject><subject>CHEMICAL REACTIONS</subject><subject>CHEMISORPTION</subject><subject>DICARBOXYLIC ACIDS</subject><subject>ELECTRON SPECTROSCOPY</subject><subject>ELEMENTS</subject><subject>HEAT TREATMENTS</subject><subject>HETEROGENEOUS CATALYSIS</subject><subject>HYDROGEN</subject><subject>HYDROGENATION</subject><subject>INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY</subject><subject>MALEIC ACID</subject><subject>METALS</subject><subject>NICKEL</subject><subject>NITRO COMPOUNDS</subject><subject>NITROBENZENE</subject><subject>NONMETALS</subject><subject>ORGANIC ACIDS</subject><subject>ORGANIC COMPOUNDS</subject><subject>ORGANIC NITROGEN COMPOUNDS</subject><subject>OXIDATION</subject><subject>PHOTOELECTRON SPECTROSCOPY</subject><subject>REDUCTION</subject><subject>SEPARATION PROCESSES</subject><subject>SORPTION</subject><subject>SORPTIVE PROPERTIES</subject><subject>SPECTROSCOPY</subject><subject>STRUCTURAL CHEMICAL ANALYSIS</subject><subject>SURFACE PROPERTIES</subject><subject>TEMPERATURE DEPENDENCE</subject><subject>TEMPERATURE RANGE</subject><subject>TEMPERATURE RANGE 0400-1000 K</subject><subject>TRANSITION ELEMENTS</subject><subject>X-RAY SPECTROSCOPY</subject><issn>0021-9517</issn><issn>1090-2694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><recordid>eNp1kE1LAzEQhoMoWKtXz8Fzd83sR3ZzLKV-QFHReg4xmdDUdlOSVOy_d9d69TQwvO_DzEPINbAcGOO3a61SDkKUOUBTnpARMMGygovqlIwYKyATNTTn5CLGNWMAdd2OCC5XSOfWok7UW_qKxn_TZUCVttj1q46mPvCWwl6nfVCbCZ2a6MMuuS-cUNUZOlNJbQ7JafoS_A5Dchh_UarDA31y-hM3l-TMqk3Eq785Ju938-XsIVs83z_OpotMl5VIGRhEo9v-_IrzirXYNhYbYeq6AdRWtEY0wEXdskpwZUC1RSWsKD6gZFYjK8fk5sj1MTkZtUuoV9p3Xf-e5AXwqmr6UH4M6eBjDGjlLritCgcJTA4m5WBSDiblYLIvtMcC9qd_OQwDGTuNxoUBbLz7r_oDGHJ53Q</recordid><startdate>19930601</startdate><enddate>19930601</enddate><creator>Mikhailenko, S.D.</creator><creator>Khodareva, T.A.</creator><creator>Leongardt, E.V.</creator><creator>Lyashenko, A.I.</creator><creator>Fasman, A.B.</creator><general>Elsevier Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>OTOTI</scope></search><sort><creationdate>19930601</creationdate><title>The Effect of Redox Treatment on the Structural, Adsorptive, and Catalytic Properties of Raney Nickel</title><author>Mikhailenko, S.D. ; Khodareva, T.A. ; Leongardt, E.V. ; Lyashenko, A.I. ; Fasman, A.B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c349t-1deedc8117466408e87fe79d5571ecf98d97169580496ad1a8249f92b130fce03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>400201 - Chemical & Physicochemical Properties</topic><topic>ADSORPTION</topic><topic>ANNEALING</topic><topic>CARBOXYLIC ACIDS</topic><topic>CATALYSIS</topic><topic>CATALYSTS</topic><topic>CATALYTIC EFFECTS</topic><topic>CHEMICAL REACTIONS</topic><topic>CHEMISORPTION</topic><topic>DICARBOXYLIC ACIDS</topic><topic>ELECTRON SPECTROSCOPY</topic><topic>ELEMENTS</topic><topic>HEAT TREATMENTS</topic><topic>HETEROGENEOUS CATALYSIS</topic><topic>HYDROGEN</topic><topic>HYDROGENATION</topic><topic>INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY</topic><topic>MALEIC ACID</topic><topic>METALS</topic><topic>NICKEL</topic><topic>NITRO COMPOUNDS</topic><topic>NITROBENZENE</topic><topic>NONMETALS</topic><topic>ORGANIC ACIDS</topic><topic>ORGANIC COMPOUNDS</topic><topic>ORGANIC NITROGEN COMPOUNDS</topic><topic>OXIDATION</topic><topic>PHOTOELECTRON SPECTROSCOPY</topic><topic>REDUCTION</topic><topic>SEPARATION PROCESSES</topic><topic>SORPTION</topic><topic>SORPTIVE PROPERTIES</topic><topic>SPECTROSCOPY</topic><topic>STRUCTURAL CHEMICAL ANALYSIS</topic><topic>SURFACE PROPERTIES</topic><topic>TEMPERATURE DEPENDENCE</topic><topic>TEMPERATURE RANGE</topic><topic>TEMPERATURE RANGE 0400-1000 K</topic><topic>TRANSITION ELEMENTS</topic><topic>X-RAY SPECTROSCOPY</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mikhailenko, S.D.</creatorcontrib><creatorcontrib>Khodareva, T.A.</creatorcontrib><creatorcontrib>Leongardt, E.V.</creatorcontrib><creatorcontrib>Lyashenko, A.I.</creatorcontrib><creatorcontrib>Fasman, A.B.</creatorcontrib><collection>CrossRef</collection><collection>OSTI.GOV</collection><jtitle>Journal of catalysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mikhailenko, S.D.</au><au>Khodareva, T.A.</au><au>Leongardt, E.V.</au><au>Lyashenko, A.I.</au><au>Fasman, A.B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Effect of Redox Treatment on the Structural, Adsorptive, and Catalytic Properties of Raney Nickel</atitle><jtitle>Journal of catalysis</jtitle><date>1993-06-01</date><risdate>1993</risdate><volume>141</volume><issue>2</issue><spage>688</spage><epage>699</epage><pages>688-699</pages><issn>0021-9517</issn><eissn>1090-2694</eissn><abstract>The effect on Raney nickel catalyst of annealing in hydrogen, and of mild oxidation and subsequent reduction have been studied. The properties investigated are the structure, hydrogen adsorption, and activity for nitrobenzene and potassium maleate liquid-phase hydrogenation. Characterization involved X-ray line broadening, adsorption, and capillary condensation of Ar, XPS, and thermoprogrammed reduction. Thermodesorption studies indicate two forms of adsorbed hydrogen, one of which is a weakly bound molecular form and does not depend on treatment, while the other is strongly bound atomic hydrogen whose amount decreases with increase in the annealing temperature. Annealing in hydrogen at T ≥ 200°C causes sintering of the catalysts and a decrease in their activity. Mild oxidation leads to formation of a protective film from nonstoichiometric nickel-oxygen compounds on the Raney Ni surface, preventing it from deep oxidation in the air. A passivated catalyst can be reactivated by heating at 100-300°C in hydrogen, after which the activity for hydrogenation is on par with that of newly prepared catalyst.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><doi>10.1006/jcat.1993.1173</doi><tpages>12</tpages></addata></record> |
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subjects | 400201 - Chemical & Physicochemical Properties ADSORPTION ANNEALING CARBOXYLIC ACIDS CATALYSIS CATALYSTS CATALYTIC EFFECTS CHEMICAL REACTIONS CHEMISORPTION DICARBOXYLIC ACIDS ELECTRON SPECTROSCOPY ELEMENTS HEAT TREATMENTS HETEROGENEOUS CATALYSIS HYDROGEN HYDROGENATION INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY MALEIC ACID METALS NICKEL NITRO COMPOUNDS NITROBENZENE NONMETALS ORGANIC ACIDS ORGANIC COMPOUNDS ORGANIC NITROGEN COMPOUNDS OXIDATION PHOTOELECTRON SPECTROSCOPY REDUCTION SEPARATION PROCESSES SORPTION SORPTIVE PROPERTIES SPECTROSCOPY STRUCTURAL CHEMICAL ANALYSIS SURFACE PROPERTIES TEMPERATURE DEPENDENCE TEMPERATURE RANGE TEMPERATURE RANGE 0400-1000 K TRANSITION ELEMENTS X-RAY SPECTROSCOPY |
title | The Effect of Redox Treatment on the Structural, Adsorptive, and Catalytic Properties of Raney Nickel |
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