TY - JOUR
T1 - Characteristics on HDS over amorphous silica-alumina in single and dual catalytic bed system for gas oil
AU - Park, Joo Il
AU - Nakano, Koji
AU - Kim, Young Kwang
AU - Miyawaki, Jin
AU - Yoon, Seong Ho
AU - Mochida, Isao
N1 - Funding Information:
This work was supported financially by the JCCP as part of a cooperative agreement between Japan and Saudi Arabia. This work was carried out within the framework of the Global-Center of Excellence (G-COE) of Novel Carbon Resource Sciences at Kyushu University.
PY - 2011/4/30
Y1 - 2011/4/30
N2 - Deep hydrodesulfurization (HDS) was investigated over amorphous silica-alumina (ASA), produced using various synthetic methods as supports for NiMo catalysts, in single and dual catalytic bed systems. NiMoS active components supported on ASA-2 (ASA from synthetic method 2) achieved S levels of 4.5 and 3.0 ppm at 345 and 360 °C, respectively, in single catalytic beds, which was the highest HDS reactivity. Dual catalytic beds were introduced to inhibit excess hydro-cracking of C species in gas oil. For the dual catalytic combination of LX6 (commercial catalyst for reactive S species) and NMASA-2 (NiMoS supported on ASA-2), the S levels were 5.4 and 2 ppm at 345 and 360 °C, respectively, indicating that the performance was enhanced at higher temperatures, likely due to improved activity for refractory S species. The increased reactivity for HDS over NMASA-2 was related to the strong acidity of this support due to tetrahedrally coordinated Al species. In addition, the smaller homogeneous particle size of the support influenced the HDS catalytic performance. Moreover, weaker interactions between the Mo and ASA-2 in NMASA-2 improved the HDS reactivity, as confirmed by laser Raman spectroscopy.
AB - Deep hydrodesulfurization (HDS) was investigated over amorphous silica-alumina (ASA), produced using various synthetic methods as supports for NiMo catalysts, in single and dual catalytic bed systems. NiMoS active components supported on ASA-2 (ASA from synthetic method 2) achieved S levels of 4.5 and 3.0 ppm at 345 and 360 °C, respectively, in single catalytic beds, which was the highest HDS reactivity. Dual catalytic beds were introduced to inhibit excess hydro-cracking of C species in gas oil. For the dual catalytic combination of LX6 (commercial catalyst for reactive S species) and NMASA-2 (NiMoS supported on ASA-2), the S levels were 5.4 and 2 ppm at 345 and 360 °C, respectively, indicating that the performance was enhanced at higher temperatures, likely due to improved activity for refractory S species. The increased reactivity for HDS over NMASA-2 was related to the strong acidity of this support due to tetrahedrally coordinated Al species. In addition, the smaller homogeneous particle size of the support influenced the HDS catalytic performance. Moreover, weaker interactions between the Mo and ASA-2 in NMASA-2 improved the HDS reactivity, as confirmed by laser Raman spectroscopy.
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U2 - 10.1016/j.cattod.2010.10.083
DO - 10.1016/j.cattod.2010.10.083
M3 - Article
AN - SCOPUS:79955050259
VL - 164
SP - 100
EP - 106
JO - Catalysis Today
JF - Catalysis Today
SN - 0920-5861
IS - 1
ER -