Investigating multi-functional traits of metal-substituted vanadate catalysts in expediting NOx reduction and poison degradation at low temperatures
- Authors
- Kim, Jongsik; Kim, Dong Ho; Ha, Heon Phil
- Issue Date
- 2020-10-05
- Publisher
- ELSEVIER
- Citation
- JOURNAL OF HAZARDOUS MATERIALS, v.397
- Abstract
- Catalysts are severely poisoned by ammonium sulfate (AS) and ammonium bisulfate (ABS) during selective catalytic NOx reduction (SCR) at low temperatures. To circumvent this issue, metal-substituted vanadates (MV2O6, M = Mn, Co, Ni, or Cu) supported on TiO2 were synthesized and functionalized with SOY2- to form M-1 (S) catalysts (Y = 3 or 4). The Mn-1 (S) could balance pre-factor and energy barrier required for the SCR, thereby exhibiting the highest NOx consumption rate (activity) among the M-1 (S) catalysts. The Mn-1 (S) also had desirable redox property, leading to the best SCR performance maximum-obtainable at low temperatures. Notably, the Mn-1 (S) substantially reduced the thermal energy needed to decompose AS/ABS poisons. Such unique feature of the Mn-1 (S) was pronounced when the Mn-1 (S) was promoted by Sb (Mn-1-Sb (S)). The resulting Mn-1-Sb (S) showed the best SCR performance among all catalysts tested. The Mn-1-Sb (S) could minimize the deposition of AS/ABS on the surface and unprecedentedly recovered its performance after regeneration even in the presence of NOx, NH3, SO2, and H2O at 260 - 280 degrees C. The temperatures required for the regeneration of the Mn-1-Sb (S) were reduced by 100 degrees C or more in comparison with those of SCR catalysts reported previously.
- Keywords
- NITRIC-OXIDE; MNOX/TIO2 CATALYST; ACTIVE-SITES; SCR; AMMONIA; SO2; NH3; MECHANISM; KINETICS; NH3-SCR; NITRIC-OXIDE; MNOX/TIO2 CATALYST; ACTIVE-SITES; SCR; AMMONIA; SO2; NH3; MECHANISM; KINETICS; NH3-SCR; Selective catalytic NOx reduction; Metal vanadate; Kinetics; Ammonium (bi)sulfate; Poison degradation; Regeneration
- ISSN
- 0304-3894
- URI
- https://pubs.kist.re.kr/handle/201004/118004
- DOI
- 10.1016/j.jhazmat.2020.122671
- Appears in Collections:
- KIST Article > 2020
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