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Zeolites physical properties

This is the first monograph that was devoted to structure, chemistry and use of zeolites. It reviews zeolite synthesis to 1973, gives a detailed structural description of synthetic and mineral zeolites, illustrates their physical properties and describes applications. [Pg.2793]

MOFs can be considered as organic zeolite analogs, as their pore architectures are often reminiscent of those of zeolites a comparison of the physical properties of a series of MOFs and of zeolite NaY has been provided in Table 4.1. Although such coordinative bonds are obviously weaker than the strong covalent Si-O and Al-O bonds in zeolites, the stability of MOF lattices is remarkable, especially when their mainly organic composition is taken into account. Thermal decomposition generally does not start at temperatures below 300 °C [3, 21], and, in some cases. [Pg.74]

Shape selectivity and orbital confinement effects are direct results of the physical dimensions of the available space in microscopic vessels and are independent of the chemical composition of nano-vessels. However, the chemical composition in many cases cannot be ignored because in contrast to traditional solution chemistry where reactions occur primarily in a dynamic solvent cage, the majority of reactions in nano-vessels occur in close proximity to a rigid surface of the container (vessel) and can be influenced by the chemical and physical properties of the vessel walls. Consequently, we begin this review with a brief examination of both the shape (structure) and chemical compositions of a unique set of nano-vessels, the zeolites, and then we will move on to examine how the outcome of photochemical reactions can be influenced and controlled in these nanospace environments. [Pg.226]

The technology and chemistry of isoalkane-alkene alkylation have been thoroughly reviewed for both liquid and solid acid catalysts (15) and for solid acid catalysts alone (16). The intention of this review is to provide an up-to-date overview of the alkylation reaction with both liquid and solid acids as catalysts. The focus is on the similarities and differences between the liquid acid catalysts on one hand and solid acid catalysts, especially zeolites, on the other. Thus, the reaction mechanism, the physical properties of the individual catalysts, and their consequences for successful operation are reviewed. The final section is an overview of existing processes and new process developments utilizing solid acids. [Pg.255]

If one examines the evolution of new zeolite structures over the past decade the most interesting discoveries have been made with high silica compositions. Many of these phases can be prepared in essentially all silica forms. Purists would prefer to classify such molecular sieves as organosilicates or porosils (1), in part because the physical properties differ from more classical low Si/Al ratio zeolites. In particular, the high silica zeolites tend to be more thermally stable and chemically robust. Additionally, the higher the Si/Al ratio the more hydrophobic the zeolite. These features are desirable for catalysts that may be used in catalytic processes such as cracking (3). [Pg.220]

Ethylbenzene plants, 23 330-331 Ethylbenzene-styrene complex, 23 328 Ethylbenzene synthesis molecular sieves in, 16 845 zeolite-based alkylation in, 23 331-333 Ethyl benzoate, 3 635 Ethyl P-D-glucopyranoside, 4 701 7-Ethylbicyclooxazolidine, antimicrobial used in cosmetics, 7 831t Ethyl bromide, physical properties of, 4 351t... [Pg.332]

The foundation of equilibrium-selective adsorption is based on differences in the equilibrium selectivity of the various adsorbates with the adsorbent While all the adsorbates have access to the adsorbent sites, the specific adsorbate is selectively adsorbed based on differences in the adsorbate-adsorbent interaction. This in turn results in higher adsorbent selectivity for one component than the others. One important parameter that affects the equilibrium-selective adsorption mechanism is the interaction between the acidic sites of the zeolite and basic sites of the adsorbate. Specific physical properties of zeolites, such as framework structure, choice of exchanged metal cations, Si02/Al203 ratio and water content can be... [Pg.211]

J.A. (1998) Influence of the activation temperature on the physical properties and catalytic activity of La-X zeolites for isobutane/n-butene alkylation. Micropor. Mesopor. Mater., 22, 379-388. [Pg.529]

The term fibrous, as applied to zeolites, does not necessarily indicate flexibility. Flexibility, however, is one of the physical properties of cotton stone found on the Isle of Skye, Scotland. This locality provides a feathery sample of mesolite, (Na2Ca2Al6SigO30 8H2O), whose composition and structure place it in the same group as natrolite. The similarity between appearance of this sample and that of the mountain flax variety of palygorskite emphasizes the difficulty of identifying fibrous minerals based on morphology alone. [Pg.71]

Zeolite, zeolite group A collective term for a family of aluminosilicate minerals characterized by framework structures that allow easy access and exchange of cations and small molecules (see chapter 2), The name derives from the Greek terms zein, meaning to boil, and lithos, meaning stone. The term is also applied to synthetic materials of comparable composition, crystal structure, and physical properties (see chapter 2). [Pg.197]

To be able to select an optimal residue catalyst, many parameters have been proposed such as the pore volume, the total surface area, and the zeolite to matrix surface area ratio (ZSA/MSA). But the only strong correlation we have found between the catalyst performance and physical properties when North Sea long residue has been used as feed, is between the ZSA/MSA ratio and the catalyst performance [13]. [Pg.67]

Synthesis and Characterisation of Ferrisilicates 47 Table 3. Physical properties of ferrisilicate analogs of zeolites... [Pg.47]

Five zeolite minerals have been considered identical with mordenite with space group Cmcm. The possibility of a family of structures is considered four related ordered structures including Cmcm are proposed. Two of these (Cmcm and Imcm) have a one-dimensional system of large pores. The remaining pair (Cmmm and Immm) have a two-dimensional pore system with a second set of smaller channels. X-ray diffraction results show that synthetic and most mineral specimens have the Cmcm structure but also reveal mixtures of Cmmm, Immm, and Imcm with the Cmcm structure in three mineral specimens. Electron diffraction examination of a ptilolite sample reveals the Cmcm structure with an inter growth of the idealized structure Cmmm. Further tentative evidence for the existence of more than one ((mordenitef) framework structure, based on physical property characteristics, is discussed. [Pg.59]

Tihe presence of exchangeable cations, framework oxygens, cavities of A different sizes, and previously adsorbed water molecules makes the interaction of water with zeolites complicated (1). As a result, in zeolites, water molecules with different physical properties exist, from tightly bound to liquid-like water. This was shown by NMR measurements (2,3 4) ... [Pg.103]

This study showed that the overall crystallization processes for mor-denite, zeolite X, and zeolite A were similar. However, the physical properties of the crystallizing system determine the rate-limiting step for a particular zeolite synthesis. In the case of mordenite in which both the viscosity of the batch composition and the morphology of seed crystals were varied, it was observed that diffusion in the liquid phase was the ratedetermining step. For zeolite X the actual growth rate on the crystal-liquid interface was the rate-limiting factor as shown by identical conversion rates for the seeded and unseeded systems. For zeolite A in the system chosen, both processes influenced the conversion rate. [Pg.154]

Very often the liquids to be processed may be contaminated with substances detrimental to some types of zeolites consequently a complete knowledge of the process stream composition and physical properties must be available before preliminary sieve selection can be made. In the absence of prior knowledge of separation factors, competitive co-adsorption, environmental stability, regeneration techniques, or irreversible zeolite contamination, zeoli te contamination, zeolite specification must be proceded by time-con-... [Pg.201]

Improved NMR, XRD, neutron-diffraction, IR, and adsorption techniques are helping to sort out the physical properties of these various A1 species in the dealuminated zeolite Y samples, and their relationship to catalytic activity. [Pg.47]

Although ZOLs have physical properties similar to those of their inorganic counterparts, they exhibit a higher hydrophobicity because of the presence of the organic framework group. This could be exemplarily shown for ZOL-A by the much higher adsorption capacity for n-hexane in comparison to its inorganic counterpart zeolite A.81... [Pg.53]

Table 6.7 displays some physical properties of zeolites. A study issued from industry [8] demonstrates the significant role of mass-transfer resistances, even for small particles below 1 mm, reporting that pore diffusion may decrease the effectiveness from low to very low values (0.4 to 0.06). The external mass-transfer resistance is much less important. In consequence, in commercial operation only a small part of the catalyst is effectively used, typically less than 10%. Since the... [Pg.179]

Alkylation of Benzene by Propylene to Cumene Table 6.7 Physical properties of a zeolite catalyst. [Pg.180]

Chemical analyses and physical property measurements made on the starting materials and the products of the ammonium fluotitanate reactions are shown in Table 2. The analytical data for the products of the iron ammonium fluoride reaction are shown in Table 3. Following treatment, the various zeolite products contained up to 16.1 wt.% Ti02 in the zeolites treated with ammonium fluotitanate, and up to 16.9 wt.% Fe203 in the zeolites treated with ammonium Iron fluoride. X-ray powder diffraction intensity is decreased in the substituted products, but retention of oxygen and water adsorption capacity indicates that pore volume has been retained. No extraneous peaks due to other crystalline phases were observed in the X-ray powder diffraction patterns of well washed products. [Pg.423]

Table 2. Chemical Analyses and Physical Property Measurements of the Starting Zeolites and the Products of the Ammonium Titanium Fluoride Reaction... Table 2. Chemical Analyses and Physical Property Measurements of the Starting Zeolites and the Products of the Ammonium Titanium Fluoride Reaction...
Semiconductor nanoclusters (quantum dots) possess chemical and physical properties that differ substantially from those of the analogous bulk solids [36-38]. Quantum dots have been synthesized using hosts such as zeolites [39], porous glass [40], micelles [41], membranes [42], and anionic polymers [43]. The synthesis and characterization of CdS quantum dots in dendrimer hosts have been studied [44-48]. Here, two PAMAM dendrimers are used one is G3.5 with surface carboxyl group and the other is G4 with surface amino group. Mixing solutions of Cd2+ and S2 in pure methanol result in a yellow precipitate of... [Pg.49]

The importance of recognizing and dealing with zeolite synthesis as a kinetic process that involves the isolation of metastable phases is pointed out in this book in a variety of ways. An examination of the extensive scientific and patent literature on zeolite synthesis rapidly convinces one that a lack of understanding of this point has been a major bottleneck in the characterization of zeolite chemical and physical properties. The zeolite properties are defined not only by synthesis parameters, but also by treatment following synthesis for example, most synthesis treatment of zeolites with fluorine can be used to modify hydrophobicity drastically and increase catalytic activity for n-butane cracking. [Pg.2]


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