Mechanochemical Activation of Cu–CeO2 Mixture as a Promising Technique for the Solid-State Synthesis of Catalysts for the Selective Oxidation of CO in the Presence of H2
A new ecologically clean method for the solid-phase synthesis of oxide copper–ceria catalysts with the use of the mechanochemical activation of a mixture of Cu powder (8 wt %) with CeO 2 was developed. It was established that metallic copper was oxidized by oxygen from CeO 2 in the course of mechano...
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Veröffentlicht in: | Kinetics and catalysis 2018, Vol.59 (2), p.160-173 |
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creator | Firsova, A. A. Morozova, O. S. Vorob’eva, G. A. Leonov, A. V. Kukharenko, A. I. Cholakh, S. O. Kurmaev, E. Z. Korchak, V. N. |
description | A new ecologically clean method for the solid-phase synthesis of oxide copper–ceria catalysts with the use of the mechanochemical activation of a mixture of Cu powder (8 wt %) with CeO
2
was developed. It was established that metallic copper was oxidized by oxygen from CeO
2
in the course of mechanochemical activation. The intensity of a signal due to metallic Cu in the X-ray diffraction analysis spectra decreased with the duration of mechanochemical activation. The Cu
1+
, Cu
2+
, and Ce
3+
ions were detected on the sample surface by X-ray photoelectron spectroscopy. The application of temperature-programmed reduction (TPR) made it possible to detect two active oxygen species in the reaction of CO oxidation in the regions of 190 and 210–220°C by a TPR-H
2
method and in the regions of 150 and 180–190°C by a TPR-CO method. It is likely that the former species occurred in the catalytically active nanocomposite surface structures containing Cu–O–Ce bonds, whereas the latter occurred in the finely dispersed particles of CuO on the surface of CeO
2
. The maximum conversion of CO (98%, 165°C) reached by the mechanochemical activation of the sample for 60 min was almost the same as conversion on a supported CuO/CeO
2
catalyst. |
doi_str_mv | 10.1134/S0023158418020076 |
format | Article |
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2
was developed. It was established that metallic copper was oxidized by oxygen from CeO
2
in the course of mechanochemical activation. The intensity of a signal due to metallic Cu in the X-ray diffraction analysis spectra decreased with the duration of mechanochemical activation. The Cu
1+
, Cu
2+
, and Ce
3+
ions were detected on the sample surface by X-ray photoelectron spectroscopy. The application of temperature-programmed reduction (TPR) made it possible to detect two active oxygen species in the reaction of CO oxidation in the regions of 190 and 210–220°C by a TPR-H
2
method and in the regions of 150 and 180–190°C by a TPR-CO method. It is likely that the former species occurred in the catalytically active nanocomposite surface structures containing Cu–O–Ce bonds, whereas the latter occurred in the finely dispersed particles of CuO on the surface of CeO
2
. The maximum conversion of CO (98%, 165°C) reached by the mechanochemical activation of the sample for 60 min was almost the same as conversion on a supported CuO/CeO
2
catalyst.</description><identifier>ISSN: 0023-1584</identifier><identifier>EISSN: 1608-3210</identifier><identifier>DOI: 10.1134/S0023158418020076</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Catalysis ; Catalysts ; Cerium oxides ; Chemistry ; Chemistry and Materials Science ; Conversion ; Copper ; Copper oxides ; Nanocomposites ; Oxidation ; Physical Chemistry ; Solid phase synthesis ; Spectrum analysis ; X-ray diffraction</subject><ispartof>Kinetics and catalysis, 2018, Vol.59 (2), p.160-173</ispartof><rights>Pleiades Publishing, Ltd. 2018</rights><rights>Copyright Springer Science & Business Media 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2686-5a609e3efcf16c8bcee9c75ea98034443a3af6b90515ebbb5e483f642803b4ce3</citedby><cites>FETCH-LOGICAL-c2686-5a609e3efcf16c8bcee9c75ea98034443a3af6b90515ebbb5e483f642803b4ce3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1134/S0023158418020076$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1134/S0023158418020076$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Firsova, A. A.</creatorcontrib><creatorcontrib>Morozova, O. S.</creatorcontrib><creatorcontrib>Vorob’eva, G. A.</creatorcontrib><creatorcontrib>Leonov, A. V.</creatorcontrib><creatorcontrib>Kukharenko, A. I.</creatorcontrib><creatorcontrib>Cholakh, S. O.</creatorcontrib><creatorcontrib>Kurmaev, E. Z.</creatorcontrib><creatorcontrib>Korchak, V. N.</creatorcontrib><title>Mechanochemical Activation of Cu–CeO2 Mixture as a Promising Technique for the Solid-State Synthesis of Catalysts for the Selective Oxidation of CO in the Presence of H2</title><title>Kinetics and catalysis</title><addtitle>Kinet Catal</addtitle><description>A new ecologically clean method for the solid-phase synthesis of oxide copper–ceria catalysts with the use of the mechanochemical activation of a mixture of Cu powder (8 wt %) with CeO
2
was developed. It was established that metallic copper was oxidized by oxygen from CeO
2
in the course of mechanochemical activation. The intensity of a signal due to metallic Cu in the X-ray diffraction analysis spectra decreased with the duration of mechanochemical activation. The Cu
1+
, Cu
2+
, and Ce
3+
ions were detected on the sample surface by X-ray photoelectron spectroscopy. The application of temperature-programmed reduction (TPR) made it possible to detect two active oxygen species in the reaction of CO oxidation in the regions of 190 and 210–220°C by a TPR-H
2
method and in the regions of 150 and 180–190°C by a TPR-CO method. It is likely that the former species occurred in the catalytically active nanocomposite surface structures containing Cu–O–Ce bonds, whereas the latter occurred in the finely dispersed particles of CuO on the surface of CeO
2
. The maximum conversion of CO (98%, 165°C) reached by the mechanochemical activation of the sample for 60 min was almost the same as conversion on a supported CuO/CeO
2
catalyst.</description><subject>Catalysis</subject><subject>Catalysts</subject><subject>Cerium oxides</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Conversion</subject><subject>Copper</subject><subject>Copper oxides</subject><subject>Nanocomposites</subject><subject>Oxidation</subject><subject>Physical Chemistry</subject><subject>Solid phase synthesis</subject><subject>Spectrum analysis</subject><subject>X-ray diffraction</subject><issn>0023-1584</issn><issn>1608-3210</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kc1KAzEUhYMoWKsP4C7gejR_k84spagVWipU10MmvdNGpokmqdid7-Bj-FY-iZlW6EJcJdzznXO4XITOKbmklIurGSGM07wQtCCMkIE8QD0qSZFxRskh6nVy1unH6CSEZ0KIoKLsoa8J6KWyTi9hZbRq8bWO5k1F4yx2DR6uvz8-hzBleGLe49oDVgEr_ODdygRjF_gx2a15XQNunMdxCXjmWjPPZlHF9N_YNAombLNUVO0mxLBHoYWuDvD03cz3pVNs7BZ48BDAauimI3aKjhrVBjj7ffvo6fbmcTjKxtO7--H1ONNMFjLLlSQlcGh0Q6Uuag1Q6kEOqiwIF0JwxVUj65LkNIe6rnMQBW-kYEmuhQbeRxe73Bfv0mYhVs9u7W2qrBhhdCBlWQwSRXeU9i4ED0314s1K-U1FSdXdpPpzk-RhO09IrF2A3yf_b_oBQ-aPzw</recordid><startdate>2018</startdate><enddate>2018</enddate><creator>Firsova, A. A.</creator><creator>Morozova, O. S.</creator><creator>Vorob’eva, G. A.</creator><creator>Leonov, A. V.</creator><creator>Kukharenko, A. I.</creator><creator>Cholakh, S. O.</creator><creator>Kurmaev, E. Z.</creator><creator>Korchak, V. N.</creator><general>Pleiades Publishing</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>2018</creationdate><title>Mechanochemical Activation of Cu–CeO2 Mixture as a Promising Technique for the Solid-State Synthesis of Catalysts for the Selective Oxidation of CO in the Presence of H2</title><author>Firsova, A. A. ; Morozova, O. S. ; Vorob’eva, G. A. ; Leonov, A. V. ; Kukharenko, A. I. ; Cholakh, S. O. ; Kurmaev, E. Z. ; Korchak, V. N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2686-5a609e3efcf16c8bcee9c75ea98034443a3af6b90515ebbb5e483f642803b4ce3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Catalysis</topic><topic>Catalysts</topic><topic>Cerium oxides</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Conversion</topic><topic>Copper</topic><topic>Copper oxides</topic><topic>Nanocomposites</topic><topic>Oxidation</topic><topic>Physical Chemistry</topic><topic>Solid phase synthesis</topic><topic>Spectrum analysis</topic><topic>X-ray diffraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Firsova, A. A.</creatorcontrib><creatorcontrib>Morozova, O. S.</creatorcontrib><creatorcontrib>Vorob’eva, G. A.</creatorcontrib><creatorcontrib>Leonov, A. V.</creatorcontrib><creatorcontrib>Kukharenko, A. I.</creatorcontrib><creatorcontrib>Cholakh, S. O.</creatorcontrib><creatorcontrib>Kurmaev, E. Z.</creatorcontrib><creatorcontrib>Korchak, V. N.</creatorcontrib><collection>CrossRef</collection><jtitle>Kinetics and catalysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Firsova, A. A.</au><au>Morozova, O. S.</au><au>Vorob’eva, G. A.</au><au>Leonov, A. V.</au><au>Kukharenko, A. I.</au><au>Cholakh, S. O.</au><au>Kurmaev, E. Z.</au><au>Korchak, V. N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mechanochemical Activation of Cu–CeO2 Mixture as a Promising Technique for the Solid-State Synthesis of Catalysts for the Selective Oxidation of CO in the Presence of H2</atitle><jtitle>Kinetics and catalysis</jtitle><stitle>Kinet Catal</stitle><date>2018</date><risdate>2018</risdate><volume>59</volume><issue>2</issue><spage>160</spage><epage>173</epage><pages>160-173</pages><issn>0023-1584</issn><eissn>1608-3210</eissn><abstract>A new ecologically clean method for the solid-phase synthesis of oxide copper–ceria catalysts with the use of the mechanochemical activation of a mixture of Cu powder (8 wt %) with CeO
2
was developed. It was established that metallic copper was oxidized by oxygen from CeO
2
in the course of mechanochemical activation. The intensity of a signal due to metallic Cu in the X-ray diffraction analysis spectra decreased with the duration of mechanochemical activation. The Cu
1+
, Cu
2+
, and Ce
3+
ions were detected on the sample surface by X-ray photoelectron spectroscopy. The application of temperature-programmed reduction (TPR) made it possible to detect two active oxygen species in the reaction of CO oxidation in the regions of 190 and 210–220°C by a TPR-H
2
method and in the regions of 150 and 180–190°C by a TPR-CO method. It is likely that the former species occurred in the catalytically active nanocomposite surface structures containing Cu–O–Ce bonds, whereas the latter occurred in the finely dispersed particles of CuO on the surface of CeO
2
. The maximum conversion of CO (98%, 165°C) reached by the mechanochemical activation of the sample for 60 min was almost the same as conversion on a supported CuO/CeO
2
catalyst.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><doi>10.1134/S0023158418020076</doi><tpages>14</tpages></addata></record> |
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subjects | Catalysis Catalysts Cerium oxides Chemistry Chemistry and Materials Science Conversion Copper Copper oxides Nanocomposites Oxidation Physical Chemistry Solid phase synthesis Spectrum analysis X-ray diffraction |
title | Mechanochemical Activation of Cu–CeO2 Mixture as a Promising Technique for the Solid-State Synthesis of Catalysts for the Selective Oxidation of CO in the Presence of H2 |
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