Abstract:An alumina support was modified by fluorine via impregnation to investigate the effect of fluoride content on the reactivity of Ni-Mo/Al 2 O 3 catalyst. The catalyst was characterized by X-ray diffraction, N 2 adsorption-desorption (Brunauer-Emmett-Teller) isotherms, temperature-programmed desorption of ammonia, X-ray photoelectron spectroscopy and high-resolution transmission electron microscopy. Sulfur etherification performance of the catalyst was studied using a fixed-bed reactor. The results show that inc… Show more
“…And the tetravalent Mo ions mainly existing in the form of fully sulfurized MoS 2 , which is closely related with the naphthalene hydrogenation activity. , The binding energies for the Mo 3d 5/2 and 3d 3/2 of Mo 5+ corresponding to the incompletely sulfurized MoS x O y intermediates are located at 230.8 and 233.9 eV. The binding energies of Mo 6+ 3d 5/2 and 3d 3/2 appearing at 233.2 and 236.3 eV correspond to the unsulfurized MoO 3 . − Furthermore, the signal ascribed to S 2– is about at 226.9 eV.…”
Section: Results
and Discussionmentioning
confidence: 93%
“…The binding energies of Mo 6+ 3d 5/2 and 3d 3/2 appearing at 233.2 and 236.3 eV correspond to the unsulfurized MoO 3 . 32 − 34 Furthermore, the signal ascribed to S 2– is about at 226.9 eV.…”
The MoS 2 /ACx catalyst for hydrogenation of naphthalene to tetralin was prepared with untreated and modified activated carbon (ACx) as support and characterized by X-ray powder diffraction, Brunauer−Emmett−Teller, scanning electron microscopy, temperature-programmed desorption of ammonia, Xray photoelectron spectroscopy, and scaning transmission electron microscopy. The results show that the modification of activated carbon by HNO 3 changes the physical and chemical properties of activated carbon (AC), which mainly increases the micropore surface area of AC from 1091 to 1209 m 2 /g, increases the micropore volume of AC from 0.444 to 0.487 cm 3 /g, increases the oxygen-containing functional groups of AC from 5.46 to 7.52, and increases the acidity of catalysts from 365.7 to 559.2 mmol/g. The modified catalyst showed good catalytic performance, and the appropriate HNO 3 concentration is very important for the modified of activated carbon. Among all the catalysts used in this study, the MoS 2 /AC3 catalyst could achieve the highest yield of tetralin. It can be attributed to the moderate acidity of the catalyst, reducing the cracking of hydrogenation products. Also, the proper hydrogenation activity of MoS 2 and the appropriate increase of oxygen-containing functional groups on the surface of modified activated carbon are beneficial to the dispersion of active components on the support, increasing the yield of tetralin. The catalytic performance of MoS 2 /AC3 is better than that of MoS 2 /Al 2 O 3 catalyst, and the two catalysts show different hydrogenation paths of naphthalene.
“…And the tetravalent Mo ions mainly existing in the form of fully sulfurized MoS 2 , which is closely related with the naphthalene hydrogenation activity. , The binding energies for the Mo 3d 5/2 and 3d 3/2 of Mo 5+ corresponding to the incompletely sulfurized MoS x O y intermediates are located at 230.8 and 233.9 eV. The binding energies of Mo 6+ 3d 5/2 and 3d 3/2 appearing at 233.2 and 236.3 eV correspond to the unsulfurized MoO 3 . − Furthermore, the signal ascribed to S 2– is about at 226.9 eV.…”
Section: Results
and Discussionmentioning
confidence: 93%
“…The binding energies of Mo 6+ 3d 5/2 and 3d 3/2 appearing at 233.2 and 236.3 eV correspond to the unsulfurized MoO 3 . 32 − 34 Furthermore, the signal ascribed to S 2– is about at 226.9 eV.…”
The MoS 2 /ACx catalyst for hydrogenation of naphthalene to tetralin was prepared with untreated and modified activated carbon (ACx) as support and characterized by X-ray powder diffraction, Brunauer−Emmett−Teller, scanning electron microscopy, temperature-programmed desorption of ammonia, Xray photoelectron spectroscopy, and scaning transmission electron microscopy. The results show that the modification of activated carbon by HNO 3 changes the physical and chemical properties of activated carbon (AC), which mainly increases the micropore surface area of AC from 1091 to 1209 m 2 /g, increases the micropore volume of AC from 0.444 to 0.487 cm 3 /g, increases the oxygen-containing functional groups of AC from 5.46 to 7.52, and increases the acidity of catalysts from 365.7 to 559.2 mmol/g. The modified catalyst showed good catalytic performance, and the appropriate HNO 3 concentration is very important for the modified of activated carbon. Among all the catalysts used in this study, the MoS 2 /AC3 catalyst could achieve the highest yield of tetralin. It can be attributed to the moderate acidity of the catalyst, reducing the cracking of hydrogenation products. Also, the proper hydrogenation activity of MoS 2 and the appropriate increase of oxygen-containing functional groups on the surface of modified activated carbon are beneficial to the dispersion of active components on the support, increasing the yield of tetralin. The catalytic performance of MoS 2 /AC3 is better than that of MoS 2 /Al 2 O 3 catalyst, and the two catalysts show different hydrogenation paths of naphthalene.
“…HRTEM analysis was carried out to determine the morphology and distribution of MoS 2 crystallites. The representative HRTEM images of sulfided catalysts are displayed in Figure , where black threads are ascribed to MoS 2 active species. , The average slab length ( L ̅) and stacking number ( N ̅) of active species on sulfided catalysts are illustrated in Figure , and the statistical results are listed in Table . Compared with the obtained bifunctional catalysts, the reference CoMo/Al 2 O 3 catalyst has the shortest average slab length and stacking number equivalent to 2.2 and 1.7 nm, respectively, resulting in the highest dispersion of active species ( D ).…”
The acidity of bifunctional catalysts
is regarded as one of the
most important factors for FCC gasoline hydrotreatment. To investigate
the effects of acidity on catalytic performance, the CoMo/Al2O3 catalysts modified by MCM-41 and HZSM-5 were prepared
by incipient wetness impregnation. The characterization results showed
that adding molecular sieves changed the distribution of acid sites
of catalysts and had a positive impact on forming longer MoS2 slabs with a slightly higher stacking number related to better hydrodesulfurization
(HDS) performance. The results of catalytic performance indicated
that 1-octene isomerization conversion increased from 4.13 to 33.97%
with the increasing Brønsted acid site/Lewis acid site (BAS/Lewis
acid sites (LAS)) ratio by presenting stronger BAS, resulting in the
increasing selectivity of hydrodesulfurization/olefin hydrogenation
(HDS/HYDO) from 0.89 to 5.41. However, when the BAS/LAS ratio surpassed
0.46 with the presence of weaker and stronger BAS, HDS efficiencies
started decreasing. This understanding sheds light on designing hydrotreating
catalysts to produce high-quality gasoline.
“…However, conventional SAPO-11 has large submicron particles and a small external surface area (ESA), and it shows a good selectivity to mono-branched isomers but a poor selectivity to di-branched isomers in long-chain n-alkane hydroisomerization (Höchtl et al 2001;Chen et al 2017). Compared with mono-branched isomers, di-branched isomers with higher octane numbers can efficiently improve the gasoline quality (Chica and Corma 1999;Zhang et al 2017;Han et al 2020). The diameter of the Edited by Xiu-Qiu Peng di-branched isomers, such as 2,6-dimethylheptane (7.1 Å), is larger than the pore openings of (Akhmedov and Al-Khowaiter 2007).…”
To enhance the gasoline octane number, low-octane linear n-alkanes should be converted into their high-octane di-branched isomers via n-alkane hydroisomerization. Therefore, hierarchical SAPO-11-based catalysts are prepared by adding different contents of sodium dodecylbenzene sulfonate (SDBS), and they are applied in n-nonane hydroisomerization. When n(SDBS)/n(SiO2) is less than or equal to 0.125, the synthesized hierarchical molecular sieves are all pure SAPO-11, and as the SDBS content increases, the submicron particle size decreases, and the external surface area (ESA) increases. Additionally, these hierarchical SAPO-11 have smaller submicron particles and higher ESA values than conventional SAPO-11. When n(SDBS)/n(SiO2) is greater than 0.125, with increasing SDBS content (n(SDBS)/n(SiO2) = 0.25), the synthesized SAPO-11 contains amorphous materials, which leads to a decline in the ESA; with the further increase in SDBS content (n(SDBS)/n(SiO2) = 0.5), the products are all amorphous materials. These results indicate that in the case of n(SDBS)/n(SiO2) = 0.125, the synthesized SAPO-11 molecular sieve (S–S3) has the most external Brønsted acid centers and the highest ESA of these SAPO-11, and these advantages favor generation of the di-branched isomers in hydrocarbon hydroisomerization. Among these Pt/SAPO-11 catalysts, Pt/S–S3 displays the highest selectivity to entire isomers (83.4%), the highest selectivity to di-branched isomers (28.1%) and the minimum hydrocracking selectivity (15.7%) in n-nonane hydroisomerization.
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