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Perovskitecatal y stsforselectivecatal y ticreductionofNO x withNH 3
1 , 2 , 3 1 , 2 , 3 3 1 , 3
TUO Kai , ZHANGPen g , WANGLi , HUANG Yu
1.Instituteo fEarthEnvironment , ChineseAcadem yo fSciences , StateKe yLaborator yo f
,
LoessandQuaternar yGeolo gy Xi ’ an710061 , China ;
2.ChinaUniversit yo fChineseAcadem yo fSciences , Bei j in g100049 , China ;
3.Ke yLaborator yo fAerosolChemistr yandPh y sics ,
ChineseAcadem yo fSciences , Xi ’ an710061 , China
)
Abstract Ammoniaselectivecatal y ticreductionofnitro g enoxides ( NO x technolo gywithV 2O 5 G
(
WO 3 MoO 3 )/ TiO 2asthecorecatal y stiscurrentl ywidel yused.Butithasman yp roblemssuchasnarG
rowandhi g hGtem p eraturewindow , eas ytop oisonb yalkaliinactivation , vanadium'sbiolo g icaltoxicit y
andsecondar yp ollutiontotheenvironment , whichre q uireresearcherstodevelo pnewefficientandenviG
ronmentall y friendl ycatal y sts y stems.Duetotheiruni q uestructure , oodstabilit yandenvironmentall y
g
friendl ycharacteristics , erovskitematerialshavebecomearesearchhots p otinthefieldofselectivecataG
p
l y ticreductionofNO x.Wereviewdtheresearchp ro g ressof p erovskiteNH 3 GSCRcatal y stsathomeand
abroadinrecent y ears , andcom p rehensivel ydiscussedthemaint yp es , denitrificationactivit yandstrucG
tureGactivit y relationshi pof p erovskitecatal y sts.Atthesametime , theresearchp ro g ressof p erovskitein
thenewfieldof p hoto p hotoGassistedSCRtechnolo gywasintroduced.Inaddition , wesummarizedthereG
searchontheNH 3 GSCRreaction mechanism ofp erovskitecatal y sts , andp ros p ectdthep ossiblefuture
develo p mentdirectionsandresearchg oalsofthisfield.
p
Ke y words ammoniaselectivecatal y ticreduction ; erovskite ; catal y sts ; denitrificationactivit y ;
;
NO x NH 3 GSCR mechanism ; air p ollutioncontrol
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