Molecular sieving, definition

The presence of methylenic bands shifted at higher frequency in the very early stages of the polymerization reaction has also been reported by Nishimura and Thomas [114]. A few years later, Spoto et al. [30,77] reported an ethylene polymerization study on a Cr/silicalite, the aluminum-free ZSM-5 molecular sieve. This system is characterized by localized nests of hydroxyls [26,27,115], which can act as grafting centers for chromium ions, thus showing a definite propensity for the formation of mononuclear chromium species. In these samples two types of chromium are present those located in the internal nests and those located on the external surface. Besides the doublet at 2920-2850 cm two additional broad bands at 2931 and 2860 cm are observed. Even in this favorable case no evidence of CH3 groups was obtained [30,77]. The first doublet is assigned to the CH2 stretching mode of the chains formed on the external surface of the zeolite. The bands at 2931 and... 

Thus, there are two limitations of the pycnometric technique mentioned possible adsorption of guest molecules and a molecular sieving effect. It is noteworthy that some PSs, e.g., with a core-shell structure, can include some void volume that can be inaccessible to the guest molecules. In this case, the measured excluded volume will be the sum of the true volume of the solid phase and the volume of inaccessible pores. One should not absolutely equalize the true density and the density measured by a pycnometric technique (the pycnometric density) because of the three factors mentioned earlier. Conventionally, presenting the results of measurements one should define the conditions of a pycnometric experiment (at least the type of guest and temperature). For example, the definition p shows that the density was measured at 298 K using helium as a probe gas. Unfortunately, use of He as a pycnometric fluid is not a panacea since adsorption of He cannot be absolutely excluded by some PSs (e.g., carbons) even at 293 K (see van der Plas in Ref. [2]). Nevertheless, in most practically important cases the values of the true and pycnometric densities are very close [2,7],... 

Introductory Chapter 1 provides a historical overview of molecular sieve materials. Chapter 2 covers the definition of a zeolite and describes their basic and composite building units and how they are linked in zeolite frameworks. It defines pores, channels, cages and cavities and it gives references for finding detailed... 

Sample size, maximum, 223 Sensitivity (detector), 95 Separation, definition of, 4 Separation factor, 20-22, 77 Separation number, 18 Sieving, molecular sieves, 45-47. See also Size exclusion chromatography Silica, surface of, 166, 167, 236, 237 Simulated distillation, 150... 

The definitions of the moments and their relationship to the system parameters for a biporous (macropore-micropore) adsorbent such as a commercial pelleted molecular sieve are given by the following equations(15,16) ... 

Molecular sieves, however, are crystalline and have, therefore, an internal structure of regularly spaced cavities with interconnecting pores of definite size. Details of the properties peculiar to the various materials are best obtained directly from the manufacturer. The following is a brief description of these principal adsorbents. 

Although the title of this book, Perspectives in Molecular Sieve Science, avoids the zeolite definition controversy, a large majority of the research reported here centers on traditional zeolites. Only three of the 39 chapters comprising the book deal with materials that are clearly nonzeolitic Two cover clay-type derivatives, and one deals with carbon molecular sieves. Not surprisingly, interest in these materials lies in their possible use as catalysts. Only four chapters present work on mineral zeolites and three on aluminum phosphate-type molecular sieves. Two of those chapters are by workers from Union Carbide, the laboratory that did the pioneering work in this field. It is surprising that other workers have not submitted papers on the aluminum phosphates, but perhaps this situation indicates that although much activity may be underway, laboratories hesitate to publish until patent positions are established in this potentially lucrative area. Union Carbide s synthetic faujasites (zeolites X and Y) and zeolite A receive the most attention, while ZSM-5-class materials are accorded more attention than zeolite A alone. This reflects the important roles that zeolites X and Y and ZSM-5 materials have already played as catalysts. 

Very definitely wet in this context. Commercially available solvents must always be carefully dried and carefully stored, for example over molecular sieves, in order to count as very dry solvents. Very dry solvents are very unstable with respect to their dryness. 

For applications in modem technology fields, not only high surface area and large pore volume, but also a sharp pore-size distribution at a definite size and control of strrface natirre of pore walls are strongly required. In order to control the pore stmcture in carbon materials, studies on the selection of prectrrsors and preparation conditions have been extensively carried out and certain successes have been achieved [ 1-3]. Pore sizes and their distributions in adsorbents have to comply with requirements from different applications. Thus, relatively small pores are needed for gas adsorption and relatively large pores for liquid adsorption, and a very narrow PSD is reqtrired for molecular sieving applications. Macropores in carbon materials were fotmd to be effective for sorption of viscous heavy oils. Recent novel techniques to control pore stmcture in carbon materials can be expected to contribute to overcome this limitation [41-46]. 

Norton reported that isobutylene polymerizes more readily than propylene or ethylene on various molecular rieves of X and A type In the absence of any definite characterization of these products, Rhein et al. examined a variety of molecular sieves under varied conations of the reaction temperature and time for isobutylene polymerization. The various molecular rieves used are type 3A, 3A ... 

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