scholarly journals Layered Materials with Catalytic Applications: Pillared and Delaminated Zeolites from MWW Precursors

2012 ◽  
Vol 2012 ◽  
pp. 1-35 ◽  
Author(s):  
Urbano Díaz

Delaminated and pillared zeolites are an innovative family of molecular sieves which introduced a different concept inside the synthesis of active catalysts or inorganic supports. These types of materials exhibit an elevated accessibility due to their open structure, characterized by the high external surface area without imposed restrictions controlled by the pore sizes. These open zeolites are conformed by crystalline ordered (pillared zeolites) or disordered (delaminated zeolites) individual layers, exhibiting textural properties which are favorable to carry out catalytic processes in which it is necessary to employ catalysts with completely accessible active sites. The elevated external surface area of these zeolites is profitable to generate more specific organic-inorganic materials, acting in this case as stable inorganic matrixes. The preparation of this open type-zeolites family is based on the modification of, previously synthesized, zeolitic precursors which are preexpanded to obtain the final delaminated or pillared zeolites which exhibit very different physicochemical properties compared with the starting precursors. Along this paper, the most relevant MWW-type high accessible zeolitic materials will be considered. Their nature, characteristics, and reactivity will be shown in the function of the employed synthesis method for their preparation and the postsynthesis treatments carried out, tuning their properties.

2020 ◽  
Vol 10 (3) ◽  
pp. 107-114
Author(s):  
Jakkidi Krishna Reddy ◽  
Shruti Lad ◽  
Kshudiram Mantri ◽  
Jagannath Das ◽  
Ganesan Raman ◽  
...  

Abstract Removal of trace olefins from aromatic liquids was investigated on UZM-8 and MCM-22, which are the family of MWW zeolites. Both these zeolites were synthesized with similar Si/Al ratio and characterized by various techniques such as XRD, SEM, ICP, N2 adsorption, Ammonia TPD and solid-state MAS-NMR. Olefin conversion activity over UZM-8 was found to be significantly higher than that of MCM-22. In addition to this, deactivation of UZM-8 was slower than the MCM-22. UZM-8 with irregular stacking of MWW layers possess high external surface area and exposes more number of active sites to the reactant molecules. Mesopores generated due to the disordered layers of UZM-8 allows the fast diffusion of the substrate molecules in which pore clogging does not occur, thus making it more active and slow deactivation than that of MCM-22. Graphic abstract


Crystals ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 813
Author(s):  
Fen Zhang ◽  
Yunhong Luo ◽  
Lei Chen ◽  
Wei Chen ◽  
Yin Hu ◽  
...  

Nanosized zeolites with larger external surface area and decreased diffusion pathway provide many potential opportunities in adsorption, diffusion, and catalytic applications. Herein, we report a designer synthesis of ultra-fine Fe-LTL zeolite nanocrystals under very mild synthesis conditions. We prepared Fe-LTL zeolite nanocrystals synthesized using L precursor. The precursor is aging at room temperature to obtain zeolite L nuclei. In order to investigate more details of Fe-LTL zeolite nanocrystals, various characterizations including X-ray diffraction (XRD), inductively coupled plasma (ICP), diffuse reflectance ultraviolet-visible (UV-Vis) spectroscopy, confirm the tetrahedral Fe3+ species in the zeolite framework. Besides, scanning electron microscope (SEM), Fourier transform infrared spectrometer (FT-IR), dynamic light scattering (DLS) indicate that the average particle size of Fe-LTL zeolite crystals is approximately 30 nm. Thus, ultra-fine Fe-LTL zeolite with large external surface area and shorter diffusion pathway to the active sites might have great potential in the near future.


2016 ◽  
Vol 2016 ◽  
pp. 1-10 ◽  
Author(s):  
Miguel Ángel Hernández ◽  
Fernando Rojas ◽  
Roberto Portillo ◽  
Martha Alicia Salgado ◽  
Vitalii Petranovskii ◽  
...  

Our research group has developed a group of hybrid biomedical materials potentially useful in the healing of diabetic foot ulcerations. The organic part of this type of hybrid materials consists of nanometric deposits, proceeding from the Mexican medicinal plantTournefortia hirsutissimaL., while the inorganic part is composed of a zeolite mixture that includes LTA, ZSM-5, clinoptilolite, and montmorillonite (PZX) as well as a composite material, made of CaCO3and montmorillonite (NABE). The organic part has been analyzed by GC-MS to detect the most abundant components present therein. In turn, the inorganic supports were characterized by XRD, SEM, and High Resolution Adsorption (HRADS) of N2at 76 K. Through this latter methodology, the external surface area of the hybrid materials was evaluated; besides, the most representative textural properties of each substrate such as total pore volume, pore size distribution, and, in some cases, the volume of micropores were calculated. The formation and stabilization of nanodeposits on the inorganic segments of the hybrid supports led to a partial blockage of the microporosity of the LTA and ZSM5 zeolites; this same effect occurred with the NABE and PZX substrates.


2017 ◽  
Vol 64 (3-4) ◽  
pp. 155-162
Author(s):  
Aleksandra Gorączko ◽  
Andrzej Olchawa

AbstractThe paper presents results of a study on the amount of water associated with the solid phase of the clay water system at the plastic limit. Two model monomineral clays, namely kaolinite, and montmorillonite, were used in the study. The latter was obtained by gravitational sedimentation of Na-bentonite (Wyoming).The calculated mean number of water molecule layers on the external surface of montmorillonite was 14.4, and water in interlayer spaces constituted 0.3 of the water mass at the plastic limit.The number of water layers on the external surface of kaolinite particles was 63, which was related to the higher density of the surface electrical charge of kaolinite compared to that of montmorillonite.The calculations were made on the basis of the external surface area of clays and the basal spacing at the plastic limit measured by an X-ray diffraction test. The external surface area of clays was estimated by measuring sorption at a relative humidity p/p0 = 0.5.


Catalysts ◽  
2019 ◽  
Vol 9 (2) ◽  
pp. 185 ◽  
Author(s):  
Guido Giammaria ◽  
Gerard van Rooij ◽  
Leon Lefferts

The goal of this study is to develop a method to distinguish between plasma chemistry and thermal effects in a Dielectric Barrier Discharge nonequilibrium plasma containing a packed bed of porous particles. Decomposition of CaCO3 in Ar plasma is used as a model reaction and CaCO3 samples were prepared with different external surface area, via the particle size, as well as with different internal surface area, via pore morphology. Also, the effect of the CO2 in gas phase on the formation of products during plasma enhanced decomposition is measured. The internal surface area is not exposed to plasma and relates to thermal effect only, whereas both plasma and thermal effects occur at the external surface area. Decomposition rates were in our case found to be influenced by internal surface changes only and thermal decomposition is concluded to dominate. This is further supported by the slow response in the CO2 concentration at a timescale of typically 1 minute upon changes in discharge power. The thermal effect is estimated based on the kinetics of the CaCO3 decomposition, resulting in a temperature increase within 80 °C for plasma power from 0 to 6 W. In contrast, CO2 dissociation to CO and O2 is controlled by plasma chemistry as this reaction is thermodynamically impossible without plasma, in agreement with fast response within a few seconds of the CO concentration when changing plasma power. CO forms exclusively via consecutive dissociation of CO2 in the gas phase and not directly from CaCO3. In ongoing work, this methodology is used to distinguish between thermal effects and plasma–chemical effects in more reactive plasma, containing, e.g., H2.


1977 ◽  
Vol 34 (2) ◽  
pp. 225-231 ◽  
Author(s):  
Gareth C. H. Harding

A method is described for estimating the surface area of marine crustaceans. The external surface area of the euphausiid Thysanöessa raschii (M. Sars) is proportional to length2.4, dry weight0.95, and wet weight0.84. Oxygen consumption is proportional to wet weight0.82, which indicates that respiration should be proportional to respiratory surface area. The implications of this finding regarding the relations of metabolic rate, size, and surface area are discussed in a broader framework by comparing them with similar studies on vertebrates and other invertebrates.


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