Insight into N2O Formation Over Different Crystal Phases of MnO2 During Low-Temperature NH3–SCR of NO
Different crystal phases of MnO 2 were synthesized and tested for NH 3 –SCR of NO and NH 3 oxidation performances during 50–120 °C. Among those catalysts, α-MnO 2 showed the most superior SCR performance for NO x conversion and N 2 selectivity, and NH 3 species on its surface were active to react wi...
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Veröffentlicht in: | Catalysis letters 2021-10, Vol.151 (10), p.2964-2971 |
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creator | Yang, Jie Ren, Shan Su, Buxin zhou, Yuhan Hu, Guang Jiang, Lijun Cao, Jun Liu, Weizao Yao, Lu Kong, Ming Yang, Jian Liu, Qingcai |
description | Different crystal phases of MnO
2
were synthesized and tested for NH
3
–SCR of NO and NH
3
oxidation performances during 50–120 °C. Among those catalysts, α-MnO
2
showed the most superior SCR performance for NO
x
conversion and N
2
selectivity, and NH
3
species on its surface were active to react with the oxygen, while NH
2
species were also easily oxidized by the oxygen. For β-MnO
2
, NH
3 (ads, B)
species and part of NH
3 (ads, L)
species on its surface were active to react with oxygen, while NH
3 (ads, L)
species adsorbed at Lewis sites showed low reactive with O
2
, thereby producing less N
2
O and low NO conversion. γ-MnO
2
showed the similar NO
x
conversion rates and N
2
O amount generated from the NH
3
oxidation comparing to α-MnO
2
, while yielding much more N
2
O generation ratios from SCR reactions conditions. Besides, NH
3 (ads, L)
, NH
3 (ads, B),
NO
3
2−
and NH
2
species adsorbed on γ-MnO
2
surface had high reactivity and could all be consumed by oxygen rapidly. And the N
2
O formation of δ-MnO
2
mainly generated from SCR reactions conditions in the temperature range of 50–120 °C, while the adsorbed NH
3 (ads, L)
species were hard to react with O
2
.
Graphic Abstract |
doi_str_mv | 10.1007/s10562-021-03541-8 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2562077912</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2562077912</sourcerecordid><originalsourceid>FETCH-LOGICAL-c319t-2eb241f73a7f7e20d6f6d5e0f6625aa63867043dd56fb695176807e3ba37ec793</originalsourceid><addsrcrecordid>eNp9kE1OwzAQRi0EEqVwAVaWWBv809jJEqWUVioNgiJ1Z7nNuE3VxsVOQN1xB27ISUgJEjtWM4vvfaN5CF0yes0oVTeB0UhyQjkjVEQ9RuIj1GGR4iRWyey42SljRCg-O0VnIawppYliSQctR2UolqsKF2Xl8IRneOD81lSFK3H2Bh73C2vBQ1nh1O9DZTb4cWUCBOwsfigzjvu1L8olHrt3MoXtDrypag94MhRfH5_P6dMhOMnO0Yk1mwAXv7OLXgZ303RIxtn9KL0dk4VgSUU4zHmPWSWMsgo4zaWVeQTUSskjY6SIpaI9keeRtHOZREzJmCoQcyMULFQiuuiq7d1591pDqPTa1b5sTmreGKJKJYw3Kd6mFt6F4MHqnS-2xu81o_ogVLdCdSNU_wjVcQOJFgq7w8fg_6r_ob4B1hp3uA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2562077912</pqid></control><display><type>article</type><title>Insight into N2O Formation Over Different Crystal Phases of MnO2 During Low-Temperature NH3–SCR of NO</title><source>SpringerLink Journals</source><creator>Yang, Jie ; Ren, Shan ; Su, Buxin ; zhou, Yuhan ; Hu, Guang ; Jiang, Lijun ; Cao, Jun ; Liu, Weizao ; Yao, Lu ; Kong, Ming ; Yang, Jian ; Liu, Qingcai</creator><creatorcontrib>Yang, Jie ; Ren, Shan ; Su, Buxin ; zhou, Yuhan ; Hu, Guang ; Jiang, Lijun ; Cao, Jun ; Liu, Weizao ; Yao, Lu ; Kong, Ming ; Yang, Jian ; Liu, Qingcai</creatorcontrib><description>Different crystal phases of MnO
2
were synthesized and tested for NH
3
–SCR of NO and NH
3
oxidation performances during 50–120 °C. Among those catalysts, α-MnO
2
showed the most superior SCR performance for NO
x
conversion and N
2
selectivity, and NH
3
species on its surface were active to react with the oxygen, while NH
2
species were also easily oxidized by the oxygen. For β-MnO
2
, NH
3 (ads, B)
species and part of NH
3 (ads, L)
species on its surface were active to react with oxygen, while NH
3 (ads, L)
species adsorbed at Lewis sites showed low reactive with O
2
, thereby producing less N
2
O and low NO conversion. γ-MnO
2
showed the similar NO
x
conversion rates and N
2
O amount generated from the NH
3
oxidation comparing to α-MnO
2
, while yielding much more N
2
O generation ratios from SCR reactions conditions. Besides, NH
3 (ads, L)
, NH
3 (ads, B),
NO
3
2−
and NH
2
species adsorbed on γ-MnO
2
surface had high reactivity and could all be consumed by oxygen rapidly. And the N
2
O formation of δ-MnO
2
mainly generated from SCR reactions conditions in the temperature range of 50–120 °C, while the adsorbed NH
3 (ads, L)
species were hard to react with O
2
.
Graphic Abstract</description><identifier>ISSN: 1011-372X</identifier><identifier>EISSN: 1572-879X</identifier><identifier>DOI: 10.1007/s10562-021-03541-8</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Ammonia ; Catalysis ; Chemistry ; Chemistry and Materials Science ; Conversion ; Flue gas ; Industrial Chemistry/Chemical Engineering ; Low temperature ; Manganese dioxide ; Metallurgy ; Nitrous oxide ; Organometallic Chemistry ; Oxidation ; Oxygen ; Physical Chemistry ; Selectivity</subject><ispartof>Catalysis letters, 2021-10, Vol.151 (10), p.2964-2971</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC part of Springer Nature 2021</rights><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC part of Springer Nature 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c319t-2eb241f73a7f7e20d6f6d5e0f6625aa63867043dd56fb695176807e3ba37ec793</citedby><cites>FETCH-LOGICAL-c319t-2eb241f73a7f7e20d6f6d5e0f6625aa63867043dd56fb695176807e3ba37ec793</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10562-021-03541-8$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10562-021-03541-8$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids></links><search><creatorcontrib>Yang, Jie</creatorcontrib><creatorcontrib>Ren, Shan</creatorcontrib><creatorcontrib>Su, Buxin</creatorcontrib><creatorcontrib>zhou, Yuhan</creatorcontrib><creatorcontrib>Hu, Guang</creatorcontrib><creatorcontrib>Jiang, Lijun</creatorcontrib><creatorcontrib>Cao, Jun</creatorcontrib><creatorcontrib>Liu, Weizao</creatorcontrib><creatorcontrib>Yao, Lu</creatorcontrib><creatorcontrib>Kong, Ming</creatorcontrib><creatorcontrib>Yang, Jian</creatorcontrib><creatorcontrib>Liu, Qingcai</creatorcontrib><title>Insight into N2O Formation Over Different Crystal Phases of MnO2 During Low-Temperature NH3–SCR of NO</title><title>Catalysis letters</title><addtitle>Catal Lett</addtitle><description>Different crystal phases of MnO
2
were synthesized and tested for NH
3
–SCR of NO and NH
3
oxidation performances during 50–120 °C. Among those catalysts, α-MnO
2
showed the most superior SCR performance for NO
x
conversion and N
2
selectivity, and NH
3
species on its surface were active to react with the oxygen, while NH
2
species were also easily oxidized by the oxygen. For β-MnO
2
, NH
3 (ads, B)
species and part of NH
3 (ads, L)
species on its surface were active to react with oxygen, while NH
3 (ads, L)
species adsorbed at Lewis sites showed low reactive with O
2
, thereby producing less N
2
O and low NO conversion. γ-MnO
2
showed the similar NO
x
conversion rates and N
2
O amount generated from the NH
3
oxidation comparing to α-MnO
2
, while yielding much more N
2
O generation ratios from SCR reactions conditions. Besides, NH
3 (ads, L)
, NH
3 (ads, B),
NO
3
2−
and NH
2
species adsorbed on γ-MnO
2
surface had high reactivity and could all be consumed by oxygen rapidly. And the N
2
O formation of δ-MnO
2
mainly generated from SCR reactions conditions in the temperature range of 50–120 °C, while the adsorbed NH
3 (ads, L)
species were hard to react with O
2
.
Graphic Abstract</description><subject>Ammonia</subject><subject>Catalysis</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Conversion</subject><subject>Flue gas</subject><subject>Industrial Chemistry/Chemical Engineering</subject><subject>Low temperature</subject><subject>Manganese dioxide</subject><subject>Metallurgy</subject><subject>Nitrous oxide</subject><subject>Organometallic Chemistry</subject><subject>Oxidation</subject><subject>Oxygen</subject><subject>Physical Chemistry</subject><subject>Selectivity</subject><issn>1011-372X</issn><issn>1572-879X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNp9kE1OwzAQRi0EEqVwAVaWWBv809jJEqWUVioNgiJ1Z7nNuE3VxsVOQN1xB27ISUgJEjtWM4vvfaN5CF0yes0oVTeB0UhyQjkjVEQ9RuIj1GGR4iRWyey42SljRCg-O0VnIawppYliSQctR2UolqsKF2Xl8IRneOD81lSFK3H2Bh73C2vBQ1nh1O9DZTb4cWUCBOwsfigzjvu1L8olHrt3MoXtDrypag94MhRfH5_P6dMhOMnO0Yk1mwAXv7OLXgZ303RIxtn9KL0dk4VgSUU4zHmPWSWMsgo4zaWVeQTUSskjY6SIpaI9keeRtHOZREzJmCoQcyMULFQiuuiq7d1591pDqPTa1b5sTmreGKJKJYw3Kd6mFt6F4MHqnS-2xu81o_ogVLdCdSNU_wjVcQOJFgq7w8fg_6r_ob4B1hp3uA</recordid><startdate>20211001</startdate><enddate>20211001</enddate><creator>Yang, Jie</creator><creator>Ren, Shan</creator><creator>Su, Buxin</creator><creator>zhou, Yuhan</creator><creator>Hu, Guang</creator><creator>Jiang, Lijun</creator><creator>Cao, Jun</creator><creator>Liu, Weizao</creator><creator>Yao, Lu</creator><creator>Kong, Ming</creator><creator>Yang, Jian</creator><creator>Liu, Qingcai</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20211001</creationdate><title>Insight into N2O Formation Over Different Crystal Phases of MnO2 During Low-Temperature NH3–SCR of NO</title><author>Yang, Jie ; Ren, Shan ; Su, Buxin ; zhou, Yuhan ; Hu, Guang ; Jiang, Lijun ; Cao, Jun ; Liu, Weizao ; Yao, Lu ; Kong, Ming ; Yang, Jian ; Liu, Qingcai</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c319t-2eb241f73a7f7e20d6f6d5e0f6625aa63867043dd56fb695176807e3ba37ec793</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Ammonia</topic><topic>Catalysis</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Conversion</topic><topic>Flue gas</topic><topic>Industrial Chemistry/Chemical Engineering</topic><topic>Low temperature</topic><topic>Manganese dioxide</topic><topic>Metallurgy</topic><topic>Nitrous oxide</topic><topic>Organometallic Chemistry</topic><topic>Oxidation</topic><topic>Oxygen</topic><topic>Physical Chemistry</topic><topic>Selectivity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Jie</creatorcontrib><creatorcontrib>Ren, Shan</creatorcontrib><creatorcontrib>Su, Buxin</creatorcontrib><creatorcontrib>zhou, Yuhan</creatorcontrib><creatorcontrib>Hu, Guang</creatorcontrib><creatorcontrib>Jiang, Lijun</creatorcontrib><creatorcontrib>Cao, Jun</creatorcontrib><creatorcontrib>Liu, Weizao</creatorcontrib><creatorcontrib>Yao, Lu</creatorcontrib><creatorcontrib>Kong, Ming</creatorcontrib><creatorcontrib>Yang, Jian</creatorcontrib><creatorcontrib>Liu, Qingcai</creatorcontrib><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>SciTech Premium Collection</collection><collection>Materials Science Database</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Catalysis letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Jie</au><au>Ren, Shan</au><au>Su, Buxin</au><au>zhou, Yuhan</au><au>Hu, Guang</au><au>Jiang, Lijun</au><au>Cao, Jun</au><au>Liu, Weizao</au><au>Yao, Lu</au><au>Kong, Ming</au><au>Yang, Jian</au><au>Liu, Qingcai</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Insight into N2O Formation Over Different Crystal Phases of MnO2 During Low-Temperature NH3–SCR of NO</atitle><jtitle>Catalysis letters</jtitle><stitle>Catal Lett</stitle><date>2021-10-01</date><risdate>2021</risdate><volume>151</volume><issue>10</issue><spage>2964</spage><epage>2971</epage><pages>2964-2971</pages><issn>1011-372X</issn><eissn>1572-879X</eissn><abstract>Different crystal phases of MnO
2
were synthesized and tested for NH
3
–SCR of NO and NH
3
oxidation performances during 50–120 °C. Among those catalysts, α-MnO
2
showed the most superior SCR performance for NO
x
conversion and N
2
selectivity, and NH
3
species on its surface were active to react with the oxygen, while NH
2
species were also easily oxidized by the oxygen. For β-MnO
2
, NH
3 (ads, B)
species and part of NH
3 (ads, L)
species on its surface were active to react with oxygen, while NH
3 (ads, L)
species adsorbed at Lewis sites showed low reactive with O
2
, thereby producing less N
2
O and low NO conversion. γ-MnO
2
showed the similar NO
x
conversion rates and N
2
O amount generated from the NH
3
oxidation comparing to α-MnO
2
, while yielding much more N
2
O generation ratios from SCR reactions conditions. Besides, NH
3 (ads, L)
, NH
3 (ads, B),
NO
3
2−
and NH
2
species adsorbed on γ-MnO
2
surface had high reactivity and could all be consumed by oxygen rapidly. And the N
2
O formation of δ-MnO
2
mainly generated from SCR reactions conditions in the temperature range of 50–120 °C, while the adsorbed NH
3 (ads, L)
species were hard to react with O
2
.
Graphic Abstract</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s10562-021-03541-8</doi><tpages>8</tpages></addata></record> |
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issn | 1011-372X 1572-879X |
language | eng |
recordid | cdi_proquest_journals_2562077912 |
source | SpringerLink Journals |
subjects | Ammonia Catalysis Chemistry Chemistry and Materials Science Conversion Flue gas Industrial Chemistry/Chemical Engineering Low temperature Manganese dioxide Metallurgy Nitrous oxide Organometallic Chemistry Oxidation Oxygen Physical Chemistry Selectivity |
title | Insight into N2O Formation Over Different Crystal Phases of MnO2 During Low-Temperature NH3–SCR of NO |
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