scholarly journals A Ni-based catalyst with polyvinyl pyrrolidone as a dispersant supported in a pretreated fluid catalytic cracking catalyst residue for C9 petroleum resin (C9 PR) hydrogenation

2018 ◽  
Vol 5 (5) ◽  
pp. 172052 ◽  
Author(s):  
Dong Chen ◽  
Linlin Wang ◽  
Xiaopeng Chen ◽  
Xiaojie Wei ◽  
Jiezhen Liang ◽  
...  

A Ni-based catalyst (Ni-PVP/PFC3R) with polyvinyl pyrrolidone (PVP) as a dispersant supported in a pretreated fluid catalytic cracking catalyst residue (PFC3R) was synthesized and applied to C9 petroleum resin (C9 PR) hydrogenation. For comparison, a Ni catalyst without PVP (Ni/PFC3R) was prepared in the same way. Ni-PVP/PFC3R exhibited higher activity and better stability. The catalysts were characterized by X-ray diffraction, scanning electron microscope, H 2 -temperature programmed reduction/temperature programmed desorption, Fourier transform infrared spectroscopy and the Brunauer–Emmett–Teller method. The catalysts had a smaller crystallite size and stronger interactions between the Ni species and the PFC3R support in the presence of PVP. The effects of nickel loading, H 2 pressure, temperature and reaction time for C9 PR hydrogenation over Ni-PVP/PFC3R were investigated. The bromine number was reduced to 1.25 under the following conditions: nickel content of 12 wt%, PVP amount of 1.5 wt%, temperature of 270°C, H 2 pressure of 8 MPa and reaction time of 240 min.

2010 ◽  
Vol 3 (2) ◽  
pp. 118-125
Author(s):  
Hery Haerudin ◽  
Silvester Tursiloadi ◽  
Galuh Widiyarti ◽  
Wuryaningsih Sri Rahayu

Nickel catalyst has been prepared impregnation and precipitation with nickel content of 20% and 25% each using bentonite as support material. The effects of the preparation method were studied using temperature programmed oxidation (TPO) and temperature programmed reduction (TPR) and by determination of its specific surface area. The activity of catalysts has been tested in the hydrogenation of palm oil. The catalyst with 20% of nickel and prepared by impregnation shows a single peak at 301°C, compared to catalyst with 25% of nickel prepared by the same method which has a peak at 304°C and a shoulder at 330°C. The reduction curves of both catalysts, those are prepared by impregnation, show a homogeneity indicated by a high main peak at 426°C (20% Ni) and 430°C (25% Ni). The 25% nickel catalyst by impregnation has a shoulder at 508°C. The catalysts prepared by precipitation show peaks at 508°C and 661°C for 20% of Ni and peaks at 419°C and 511°C for 25% of Ni. The reduction curves of catalysts prepared by precipitation are significantly different from each other. Those are also very different comparing to the reduction curve of impregnated catalyst. The 20% precipitated nickel catalyst has a single peak at 540°C, but the 25% precipitated nickel catalyst shows peaks at 346°C and 503°C. The differences of peak position among the reduction curves of catalysts resulted in the differences of catalyst activities with the following order 20% Ni (impregnation) > 25% Ni (impregnation) > 20% Ni (precipitation) > 25% Ni (precipitation).   Keywords: bentonite, nickel catalyst, hidrogenation


2013 ◽  
Vol 1 ◽  
pp. 194308921350702
Author(s):  
Madhavi Madeti ◽  
Sharad V. Lande ◽  
Kalpana G ◽  
R. K. Mewada ◽  
R. V. Jasra

We have attempted a green alternative to reuse the spent fluid catalytic cracking (FCC) catalyst that is used in petroleum refining industry for the upgradation and purification of various petroleum streams and residues. The spent FCC zeolite–based catalyst modified by enhancing the acidic properties by incorporating Zn and In metals in the matrix. The various prepared catalysts were systematically characterized by X-ray powder diffraction and Brunauer–Emmett–Teller (BET; adsorption isotherm) surface area. The acidity of the materials was studied by temperature-programmed desorption of ammonia (NH3-TPD). The well-characterized catalysts were applied for liquid phase benzylation of o-xylene using benzyl chloride.


ACS Omega ◽  
2020 ◽  
Vol 5 (32) ◽  
pp. 20291-20298
Author(s):  
Ming Jiang ◽  
Xiaojie Wei ◽  
Xiaopeng Chen ◽  
Linlin Wang ◽  
Jiezhen Liang

Molecules ◽  
2021 ◽  
Vol 26 (8) ◽  
pp. 2289
Author(s):  
Haihui Fu ◽  
Yan Chen ◽  
Tingting Liu ◽  
Xuemei Zhu ◽  
Yufei Yang ◽  
...  

Fluid catalytic cracking (FCC) spent catalysts are the most common catalysts produced by the petroleum refining industry in China. The National Hazardous Waste List (2016 edition) lists FCC spent catalysts as hazardous waste, but this listing is very controversial in the petroleum refining industry. This study collects samples of waste catalysts from seven domestic catalytic cracking units without antimony-based passivation agents and identifies their hazardous characteristics. FCC spent catalysts do not have the characteristics of flammability, corrosiveness, reactivity, or infectivity. Based on our analysis of the components and production process of the FCC spent catalysts, we focused on the hazardous characteristic of toxicity. Our results show that the leaching toxicity of the heavy metal pollutants nickel, copper, lead, and zinc in the FCC spent catalyst samples did not exceed the hazardous waste identification standards. Assuming that the standards for antimony and vanadium leachate are 100 times higher than that of the surface water and groundwater environmental quality standards, the leaching concentration of antimony and vanadium in the FCC spent catalyst of the G set of installations exceeds the standard, which may affect the environmental quality of surface water or groundwater. The quantities of toxic substances in all spent FCC catalysts, except those from G2, does not exceed the standard. The acute toxicity of FCC spent catalysts in all installations does not exceed the standard. Therefore, we exclude “waste catalysts from catalytic cracking units without antimony-based passivating agent passivation nickel agent” from the “National Hazardous Waste List.”


Fuel ◽  
2021 ◽  
Vol 292 ◽  
pp. 120364
Author(s):  
Peipei Miao ◽  
Xiaolin Zhu ◽  
Yangling Guo ◽  
Jie Miao ◽  
Mengyun Yu ◽  
...  

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