Promotion of hydrogenation activity and sulfur resistance over Ni/ASA catalyst by support modification simultaneously with P and USY. Issue 66 (25th August 2017)
- Record Type:
- Journal Article
- Title:
- Promotion of hydrogenation activity and sulfur resistance over Ni/ASA catalyst by support modification simultaneously with P and USY. Issue 66 (25th August 2017)
- Main Title:
- Promotion of hydrogenation activity and sulfur resistance over Ni/ASA catalyst by support modification simultaneously with P and USY
- Authors:
- Cui, Sha
Ge, Jiaqi
Wang, Genggeng
Yang, Ying
Liu, Baijun - Abstract:
- Abstract : Compared to Ni/ASA (Cat), individual and simultaneous P and USY promoted ASA supported Ni catalysts display higher naphthalene hydrogenation activity, especially the simultaneous P and USY promoted catalyst. Abstract : Individual and simultaneous P and USY promoted amorphous SiO2 –Al2 O3 (ASA) supported Ni catalysts were prepared using the hydrothermal synthesis method with the assistance of cis -9-octadecenylamine. The catalysts were characterized by X-ray diffraction (XRD), N2 -adsorption and desorption, UV-vis diffuse reflectance spectroscopy, FTIR spectroscopy of adsorbed pyridine (Py-IR), transmission electron microscopy (TEM), temperature-programmed hydrogen reduction (H2 -TPR) and X-ray photoelectron spectroscopy (XPS). The effects of P and USY loading on the activity of naphthalene hydrogenation were evaluated in a fixed bed reactor under the following reaction conditions: P = 4 MPa, GHSV = 16 h −1, H2 /oil = 600 volume ratio, T = 200, 240, 280 and 320 °C. Experimental results verified that all individual P and USY modified catalysts displayed higher hydrogenation activity than the freely P and USY decorated catalyst at 200–280 °C. Furthermore, the catalyst simultaneously modified with 1.0 wt% P and 10 wt% USY had the highest hydrogenation activity and sulfur tolerance. Multiple effects, such as metal dispersion, acid amount, surface exposure of the active Ni° species and the [NiOh 2+ ]/[NiTd 2+ ] ratio were responsible for the high hydrogenation activityAbstract : Compared to Ni/ASA (Cat), individual and simultaneous P and USY promoted ASA supported Ni catalysts display higher naphthalene hydrogenation activity, especially the simultaneous P and USY promoted catalyst. Abstract : Individual and simultaneous P and USY promoted amorphous SiO2 –Al2 O3 (ASA) supported Ni catalysts were prepared using the hydrothermal synthesis method with the assistance of cis -9-octadecenylamine. The catalysts were characterized by X-ray diffraction (XRD), N2 -adsorption and desorption, UV-vis diffuse reflectance spectroscopy, FTIR spectroscopy of adsorbed pyridine (Py-IR), transmission electron microscopy (TEM), temperature-programmed hydrogen reduction (H2 -TPR) and X-ray photoelectron spectroscopy (XPS). The effects of P and USY loading on the activity of naphthalene hydrogenation were evaluated in a fixed bed reactor under the following reaction conditions: P = 4 MPa, GHSV = 16 h −1, H2 /oil = 600 volume ratio, T = 200, 240, 280 and 320 °C. Experimental results verified that all individual P and USY modified catalysts displayed higher hydrogenation activity than the freely P and USY decorated catalyst at 200–280 °C. Furthermore, the catalyst simultaneously modified with 1.0 wt% P and 10 wt% USY had the highest hydrogenation activity and sulfur tolerance. Multiple effects, such as metal dispersion, acid amount, surface exposure of the active Ni° species and the [NiOh 2+ ]/[NiTd 2+ ] ratio were responsible for the high hydrogenation activity of P and USY-promoted catalysts. … (more)
- Is Part Of:
- RSC advances. Volume 7:Issue 66(2017)
- Journal:
- RSC advances
- Issue:
- Volume 7:Issue 66(2017)
- Issue Display:
- Volume 7, Issue 66 (2017)
- Year:
- 2017
- Volume:
- 7
- Issue:
- 66
- Issue Sort Value:
- 2017-0007-0066-0000
- Page Start:
- 41460
- Page End:
- 41470
- Publication Date:
- 2017-08-25
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c7ra05413k ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4561.xml