2002
DOI: 10.1016/s0920-5861(02)00073-1
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Selective catalytic reduction of N2O and NO in a single reactor in the nitric acid industry

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Cited by 37 publications
(19 citation statements)
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“…The maximum conversion of NO is 60% on the CoO/H-ZSM-5 catalyst at 450°C and 24% on the CoO/ZrO 2 catalyst at 350°C (Table 1). A similar effect, namely, the lack of selective catalytic reduction of N 2 O, was found by van den Brink et al [14] on Co-ZSM-5 in the reaction mixture with N 2 O + NO + O 2 + H 2 O + C 3 H 8 . Table 1 using methane at temperatures 100°C less than in the case of the propane-butane mixture, i.e., methane is considerably more efficient as a reducing agent, perhaps as a consequence of the formation of an active nitromethane intermediate [15].…”
supporting
confidence: 79%
“…The maximum conversion of NO is 60% on the CoO/H-ZSM-5 catalyst at 450°C and 24% on the CoO/ZrO 2 catalyst at 350°C (Table 1). A similar effect, namely, the lack of selective catalytic reduction of N 2 O, was found by van den Brink et al [14] on Co-ZSM-5 in the reaction mixture with N 2 O + NO + O 2 + H 2 O + C 3 H 8 . Table 1 using methane at temperatures 100°C less than in the case of the propane-butane mixture, i.e., methane is considerably more efficient as a reducing agent, perhaps as a consequence of the formation of an active nitromethane intermediate [15].…”
supporting
confidence: 79%
“…Industrial N 2 O emissions can be largely abated: 98% for adipic acid (Reimer et al, 1999;WBCSD/WRI, 2005) and 80-90% (WBCSD/WRI, 2005) and even up to 90-95% (Van den Brink et al, 2002) for nitric acid. The additional costs of these options are quite low; 1 US$/tCeq for adipic acid and 1-5 US$/tCeq for nitric acid (COHERENCE, 1999;De Beer et al, 2001).…”
Section: Nitrous Oxide Emission Reductions From Industrial Sourcesmentioning
confidence: 99%
“…It would be favorable to reduce both the pollutants in one catalytic bed, using the same reducing agent as natural gas. Thus far, few papers were addressed to simultaneous selective catalytic reduction with hydrocarbons in a double catalytic bed [4][5][6][7], or in a single catalytic bed [8,9]. When a single catalyst was adopted for the simultaneous abatement, it was suggested that the nitrogen oxides partially competed for the same active sites [9].…”
Section: Introductionmentioning
confidence: 99%