mesoporous solids
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Adsorption ◽  
2021 ◽  
Author(s):  
Ronny Pini ◽  
Humera Ansari ◽  
Junyoung Hwang

AbstractGas adsorption at high pressures in porous solids is commonly quantified in terms of the excess amount adsorbed. Despite the wide spectrum of adsorbent morphologies available, the analysis of excess adsorption isotherms has mostly focused on microporous materials and the role of mesoporosity remains largely unexplored. Here, we present supercritical CO2 adsorption isotherms measured at $$T=308$$ T = 308  K in the pressure range $$p=0.02{-}21$$ p = 0.02 - 21  MPa on three adsorbents with distinct fractions of microporosity, $$\phi_2$$ ϕ 2 , namely a microporous metal-organic framework ($$\phi_2=70$$ ϕ 2 = 70 %), a micro-mesoporous zeolite ($$\phi_2=38$$ ϕ 2 = 38 %) and a mesoporous carbon ($$\phi_2<0.1$$ ϕ 2 < 0.1 %). The results are compared systematically in terms of excess and net adsorption relative to two distinct reference states–the space filled with gas in the presence/absence of adsorbent–that are defined from two separate experiments using helium as the probing gas. We discuss the inherent difficulties in extracting from the supercritical adsorption isotherms quantitative information on the properties of the adsorbed phase (its density or volume), because of the nonuniform distribution of the latter within and across the different classes of pore sizes. Yet, the data clearly reveal pore-size dependent adsorption behaviour, which can be used to identify characteristic types of isotherm and to complement the information obtained using the more traditional textural analysis by physisorption.


2020 ◽  
Vol 309 ◽  
pp. 110534 ◽  
Author(s):  
Henry R.N.B. Enninful ◽  
Daniel Schneider ◽  
Richard Kohns ◽  
Dirk Enke ◽  
Rustem Valiullin

Catalysts ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1388
Author(s):  
Anna Białas ◽  
Kamil Rugała ◽  
Cezary Czosnek ◽  
Grzegorz Mordarski ◽  
Jacek Gurgul

Cu-Ce(Mn)-Al oxide catalysts to NO removal in the broad temperature range were synthesized and tested. The precursor of copper aluminium spinel was obtained with the coprecipitation method. By this method, Cu–Al spinels with various amounts of manganese and cerium were synthesized as well. These oxides crystallized in the structure of inverse spinel; however, Ce doping caused the appearance of additional CeO2 phase as determined by XRD. The samples were mesoporous solids with moderate surface area and porosity measured by low temperature sorption of nitrogen. The addition of another metal to Cu–Al spinel caused an increase of activity in selective catalytic reduction of nitrogen oxide with ammonia. The presence of manganese caused the formation of a higher amount of N2O by-product. The catalytic activity increased with the cerium concentration. For the sample with the atomic ratio Ce0.15Cu0.18, ca. 90% of NO conversion was registered between 200 and 350 °C. As examined with XPS spectroscopy, such conversion was attained due to the good dispersion of copper on the catalyst surface. This copper was placed mainly in spinel octahedral positions which enable its easier reduction. The spinel structure causes the presence of cerium as the trivalent cation important in redox cycles with the participation of copper.


2020 ◽  
pp. 247-282
Author(s):  
Elaine A. Moore ◽  
Lesley E. Smart
Keyword(s):  

2020 ◽  
Vol 7 (1) ◽  
Author(s):  
Marisa B. Navas ◽  
José F. Ruggera ◽  
Ileana D. Lick ◽  
Mónica L. Casella

AbstractThis paper describes the preparation and characterization of MgO and ZnO-based catalysts, pure and mixed in different proportions, supported on γ-Al2O3. Their catalytic performance was studied in the transesterification of soybean oil and castor oil with methanol and butanol, attempting to produce biodiesel. XRD (X-ray diffraction), SEM–EDS (scanning electron microscopy–energy dispersive X-ray spectroscopy), CO2-adsorption and N2-adsorption allowed characterizing the prepared catalysts. The characterization results were in all cases consistent with mesoporous solids with high specific surface area. All the catalysts exhibited good results, especially in the transesterification of castor oil using butanol. For this reaction, the reuse was tested, maintaining high FABE (fatty acid butyl esters) yields after four cycles. This good performance can be attributed to the basic properties of the Mg species, and simultaneously, to the amphoteric properties of ZnO, which allow both triglycerides and free fatty acids to be converted into esters. Using these catalysts, it is possible to obtain second-generation biodiesel, employing castor oil, a raw material that does not compete with the food industry. In addition, butanol can be produced from renewable biomass.


2018 ◽  
Vol 556 ◽  
pp. 73-80 ◽  
Author(s):  
Nicolas Godard ◽  
Xavier Collard ◽  
Alvise Vivian ◽  
Lucia Anna Bivona ◽  
Sonia Fiorilli ◽  
...  

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