Efficient Hydrogenation Catalyst Designing via Preferential Adsorption Sites Construction towards Active Copper

Author(s):  
Dongcheng He ◽  
Tao Wang ◽  
Teng Li ◽  
Xinzhi Wang ◽  
Hongli Wang ◽  
...  
2020 ◽  
Vol 8 (23) ◽  
pp. 11515-11520 ◽  
Author(s):  
Eva Martínez-Ahumada ◽  
Mariana L. Díaz-Ramírez ◽  
Hugo A. Lara-García ◽  
Daryl R. Williams ◽  
Vladimir Martis ◽  
...  

MIL-101(Cr)-4F(1%) shows a high uptake and high chemical stability to dry and humid SO2 and a remarkable cyclability. In situ DRIF spectroscopy upon the adsorption of CO identified the preferential adsorption sites for this MOF material.


2007 ◽  
Vol 103 (1-3) ◽  
pp. 280-283 ◽  
Author(s):  
Siricharn S. Jirapongphan ◽  
Juliusz Warzywoda ◽  
David E. Budil ◽  
Albert Sacco

Author(s):  
Yongkang Cui ◽  
Ziyi Li ◽  
Wei Su ◽  
Yi Xing ◽  
Yingshu Liu ◽  
...  

AbstractAdsorption as an air purification method is widely employed to remove volatile organic compounds with low concentration using zeolites. In this study, ZSM-5 and LSX zeolites modified by alkali metal cations (Li+, Na+ and K+) were used as adsorbents for the abatement of toluene. The adsorption behaviors of toluene onto adsorbents with different pore sizes and cation contents were evaluated systematically based on the experiments of adsorption equilibrium, kinetic diffusion and desorption. Besides, Langmuir and Freundlich model, constant-pattern wave propagation model and Kissinger method were applied to fit with the above experimental data. The adsorption amount followed the sequence of Li-LSX > Na-LSX > K-LSX > Li-ZSM-5 > Na-ZSM-5 > K-ZSM-5 obtained from equilibrium isotherms. LSX zeolites showed twice adsorption capacity on unit volume compared to ZSM-5. The mechanisms of steric hindrances and electrostatic interactions controlling the diffusion rate under high and low concentrations were proposed, respectively. At relatively low loadings of toluene, the diffusion resistances were primarily affected by electrostatic interaction due to preferential adsorption of toluene on cationic sites. While at relatively high loadings, the diffusion resistance was mainly restricted by steric effect because of saturated cationic sites. The strength of adsorbate-adsorbent interactions was assessed by temperature programmed desorption experiments. It showed that both adsorption sites and microporous walls contributed to the desorption energy.


2001 ◽  
Vol 492 (1-2) ◽  
pp. L700-L704 ◽  
Author(s):  
L Ottaviano ◽  
E Maccallini ◽  
S Santucci

2020 ◽  
Author(s):  
Heike Knicker ◽  
Jose Maria Garcia Castro de Barragan ◽  
Elena Elena Fernandez-Boy ◽  
Michael Knicker ◽  
Regina León-Ovelar ◽  
...  

<p>Since peatlands are valuable habitats and provide important environmental services, the policy of several European countries is to decrease the use of peat in potting mixtures to preserve peat bogs as nature areas. As a consequence, alternative growing media are needed. Therefore, the impact of biochar addition to gardening soil on tomato plant growth has been investigated previously (García de Castro Barragán, 2018). Those studies revealed a positive effect on seed germination and plant development during the first growing stage. However after three months, leaf discoloration was observed and associated to the lack of macro or micronutrients. It was hypothized that adsorption of nutrients onto the biochar may have decreased their availability for plants. For a first evaluation of this hypothesis, we tested the adsorption of Cu<sup>2+ </sup>to three biochars derived from feedstocks with different chemical composition, aromaticity and content of polar groups.  We produced biochar from shrimp chitin which was highly aromatic and contained considerable amounts of N-heterocyclic aromatic structures. The biochar of shells of the oil seed of Acrocomia aculeata derived from a woody feedstock with high contribution of cellulose, but had a low charring degree. The peat biochar was prepared at a pyrolysis temperature of 500°C which resulted in a highly aromatic material.  The difference in the organic matter (OM) quality of the biochars went along with differences in their pH and electrical conductivity (EC); elemental composition and ash content. Concomitantly, different specific surface areas were measured using the BET method.</p><p>For the absorption test, copper nitrate solutions were used at increasing concentration, brought into contact with the biochar for 24 hours at 25 °C. In the equilibrium solution, the Cu<sup>2+ </sup>content was analyzed. The solid biochar was separated from the solution and dried. Due to the paramagnetic nature of Cu<sup>2+</sup>, solid-state NMR relaxometry was used to identify preferential adsorption sites within the organic network of the biochars.</p><p>Our results showed low Cu<sup>2+ </sup>adsorption for all three biochars. Neither biochar porosity, nor polarity could be identified as a responsible for Cu-adsorption. As revealed by NMR relaxation times (T<sub>1H, </sub>T<sub>1C</sub>, T<sub>1rohH</sub> and T<sub>1rohC</sub>), all organic C and H groups were affected by the interactions between OM and Cu<sup>2+</sup>, although no preferential adsorption site was revealed. We found indications that adsorbed Cu<sup>2+</sup> act as bridging agent, lowering the mobility of aromatic domains. Based on our preliminary results, we suggest that in our biochars, metals are mainly adsorbed via bonding to π-orbitals of the aromatic rings. Based on the low adsorption potential of the studied cation, we conclude further that our biochars do not sequester Cu<sup>2+</sup> (or other metals with comparable characteristics) sufficiently strong for preventing their uptake by growing plants. However, to which extend our findings may be generalized, has to be unveiled by ongoing studies.</p>


1993 ◽  
Vol 312 ◽  
Author(s):  
A. R. Avery ◽  
A. J. Mayne ◽  
C. M. Goringe ◽  
J. H. G. Owen ◽  
C. W. Smith ◽  
...  

AbstractScanning tunnelling microscopy (STM) has been used to image the adsorption of trimethylgallium (TMGa) on GaAs(001)-(2×4) surfaces prepared in situ by molecular beam epitaxy (MBE). Filled states images of the clean surface are dominated by (2×4) unit cells containing only two As dimers. Upon exposure of this surface to TMGa at room temperature, bright oval-shaped features are observed which are centred on the arsenic dimers of the unit cell. These arise from tunnelling from Ga-C bonds of the adsorbed molecules. At low coverages, preferential adsorption on unit cells adjacent to occupied sites along the [110] direction is observed. A detailed statistical analysis of a large number of adsorption sites shows that there is an increased probability of about 24% for adsorption next to a (2×4) unit cell which is occupied relative to an unoccupied one.


2020 ◽  
Vol 22 (37) ◽  
pp. 21317-21325
Author(s):  
Lisa Warczinski ◽  
Bin Hu ◽  
Till Eckhard ◽  
Baoxiang Peng ◽  
Martin Muhler ◽  
...  

Pyridinic nitrogen atoms are preferential adsorption sites for palladium nanoparticles and lead to a change of the Pd oxidation state from Pd0 to Pd2+.


Author(s):  
Marcos Rivera-Almazo ◽  
Mariana L. Díaz-Ramírez ◽  
Raymundo Hernández-Esparza ◽  
Rubicelia Vargas ◽  
Ana Martínez ◽  
...  

DRIFT spectroscopy combined with DFT and QTAIM calculations, revealed the CO preferential adsorption sites within NOTT-401.


2020 ◽  
Vol 49 (9) ◽  
pp. 2786-2793
Author(s):  
Luz J. Barrios-Vargas ◽  
José G. Ruiz-Montoya ◽  
Bruno Landeros-Rivera ◽  
J. Raziel Álvarez ◽  
Daniel Alvarado-Alvarado ◽  
...  

Benzene confinement enhances the CO2 capture while decreases the SO2 capture within InOF-1 due to the competition among molecules for the preferential adsorption sites. Pore channel view of CO2Bz@InOF-1b (left) and SO2⋯Bz@InOF-1b (right) systems.


2018 ◽  
Vol 36 (5-6) ◽  
pp. 1246-1259 ◽  
Author(s):  
C Mve Mfoumou ◽  
S Mignard ◽  
T Belin

Study of preferential adsorption sites of H2O on NaX and BaX zeolites was carried out after adsorption/desorption of carbon dioxide (CO2). The profiles of CO2 desorption revealed two distinct zones. The first one, at low temperature (T < 533 K), corresponding to physisorbed CO2 where BaX zeolite has an energy of adsorption higher than that of NaX as well as strong interactions of adsorbent/adsorbate. The second one (533–623 K) corresponds to the chemisorbed CO2. The presence of water influences CO2 adsorption. The effect is more important for NaX than for BaX. For NaX, water occupies the adsorption sites of CO2 between 373 and 483 K. In contrast, BaX preserves a majority of adsorption sites of physisorbed CO2 in the presence of water, in particular the adsorption sites located in the interval of temperature 423–533 K.


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