2015
DOI: 10.1016/j.crci.2015.05.004
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The influence of poisoning on the deactivation of DeNOx catalysts

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Cited by 12 publications
(12 citation statements)
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“…where, ∆x is the relative loss of activity, x the conversion, and indices 0 and t stand for times of exposure [81]. The blockage of active sites as a result of poisoning are discussed in detail elsewhere [62,[79][80][81][82][83]. Table 4 shows the types, treatment, and causes of catalyst deactivation.…”
Section: Catalyst Deactivationmentioning
confidence: 99%
See 1 more Smart Citation
“…where, ∆x is the relative loss of activity, x the conversion, and indices 0 and t stand for times of exposure [81]. The blockage of active sites as a result of poisoning are discussed in detail elsewhere [62,[79][80][81][82][83]. Table 4 shows the types, treatment, and causes of catalyst deactivation.…”
Section: Catalyst Deactivationmentioning
confidence: 99%
“…The term NOx is referred to as the oxides of nitrogen (NO, NO 2 , NO 3 , N 2 O 3 , N 2 O 4 , N 2 O 5 , NO, and NO 2 ) [10]. NO 2 comprises of 95% of NOx produced as a result of combustion processes and is stated to contribute to air emissions by several researchers [81,124,130]. NO 2 is a red-brown gas that can readily form nitric acid when it is reacted with H 2 O.…”
Section: Nox Removal From Flue Gasmentioning
confidence: 99%
“…Despite many advantages, catalysts tend to lose their activity over time. Kiełtyka et al [2] indicated, that in a typical coal-fired power plant with biomass co-firing, V 2 O 5 −WO 3 /TiO 2 commercial catalyst can lose 10% of its activity already after 2000 h of operation, and 20% after nearly 5000 h. According to Zheng et al [3], the rate of deactivation of V 2 O 5 −WO 3 /TiO 2 catalyst installed on a straw-fired boiler can be as high as 1% per day of operation. Eventually catalytic layers need to be replaced every 2-3 years (in commercial installations), and new ones are relatively expensive [4,5].…”
Section: Introductionmentioning
confidence: 99%
“…The major reason for V 2 O 5 −WO 3 /TiO 2 catalyst deactivation is, however, related to interactions with alkali metals present in flue gas. As the temperature required by the V 2 O 5 −WO 3 /TiO 2 catalyst is relatively high, the most common position of the SCR installation is upstream of the dust collector (called a high-dust SCR)[2,6,85]. Because of that, the catalyst surface interacts with alkali and earth alkali metals carried out by the flue gas stream.…”
mentioning
confidence: 99%
“…At the same time co-firing of coal and biomass -the method used to reduce CO2 emissions -has a negative effect on the operation of the SCR catalyst placed in the front of dust collector because of alkali and alkaline earth elements present in biomass and, consequently, in the fly ash. It leads to deterioration of the catalyst by poisoning reaction centres [2]. Placing the catalyst downstream of the dust collector would therefore allow for more efficient operation and longer catalysts life.…”
Section: Introductionmentioning
confidence: 99%