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Synthesis secondary

High crystallization rates and the possibility to stabilize X-ray amorphous phases, which exhibit ZSM-5 like properties, were among the reasons why we decided to investigate the procedure B in more detail. In order to optimize the particle size, homogeneity, morphology and composition, we have questioned more systematically the influence of secondary synthesis variables such as the pH, solvent viscosity or the nature of the alkali cation, added as chloride. [Pg.219]

The 1980s saw major developments in secondary synthesis and modification chemistry of zeolites. SUicon-enriched frameworks of over a dozen zeolites were described using methods of (i) thermochemical modification (prolonged steaming) with or without subsequent acid extraction, (ii) mild aqueous ammonium fluorosilicate chemistry, (iii) high-temperature treatment with silicon tetrachloride and (iv) low-temperature treatment with fluorine gas. Similarly, framework metal substitution using mild aqueous ammonium fluorometaUate chemistry was reported to incorporate iron, titanium, chromium and tin into zeolite frameworks by secondary synthesis techniques. [Pg.8]

Humic substances A series of relatively high-molecular-weight, yellow- to black-colored substances formed by secondary synthesis reactions. The term is used as a generic name to describe the colored material or its fractions obtained on the basis of solubility characteristics. These materials are distinctive to the soil (or sediment) environment in that they are dissimilar to the biopolymers of microorganisms and higher plants (including lignin)... [Pg.14]

Niobium and titanium incorporation in a molecular sieve can be achieved either by hydrothermal synthesis (direct synthesis) or by post-synthesis modification (secondary synthesis). The grafting method has shown promise for developing active oxidation catalyst in a simple and convenient way. Recently, the grafting of metallocene complexes onto mesoporous silica has been reported as alternate route to the synthesis of an active epoxidation catalyst [21]. Further the control of active sites, the specific removal of organic material (template or surfactant) occluded within mesoporous molecular sieves during synthesis can also be important and useful to develop an active epoxidation catalyst. Thermal method is quite often used to eliminate organic species from porous materials. However, several techniques such as supercritical fluid extraction (SFE) and plasma [22], ozone treatment [23], ion exchange [24-26] are also reported. [Pg.328]

The synthesis of titanium-containing beta zeolite has been carried out by direct hydrothermal synthesis and by secondary synthesis. In the direct synthesis with aluminum salts and titanium and silicon alkoxides, it is necessary to operate in the absence of alkalies, since these cause the formation of an amorphous precipitate containing Ti02 and Si02. Evidence for the substitution... [Pg.284]

The secondary synthesis has been carried out by reaction of beta zeolite with TiCl4 (Ferrini et al., 1992) or with ammonium titanyl oxalate (Reddy, J. S. et al., 1995). This second method appears to be more reliable, inserting Tiiv in framework positions only, while with TiCl4, Ti02 phases are also formed. [Pg.285]

The synthesis of these titanium-substituted zeolites has been described to occur by a secondary synthesis process involving the reaction of [NH4]2TiF6 with the preformed corresponding zeolite (Section IV.G). The chemical and physicochemical properties described are not sufficient to establish the presence of Tiiv ions in framework positions. The titanium concentrations reported are much higher than the maximum values observed in titanium silicates for which isomorphous substitution has been demonstrated. The possible presence of Ti02 particles has not been investigated. No indication of the properties of these materials as catalysts in reactions typical of titanium silicates has been provided. It is therefore very doubtful that real isomorphous substitution has been obtained (Skeels et al., 1989 Skeels, 1993). [Pg.287]

Ti-Beta has also been obtained by secondary synthesis, by reaction of beta zeolite with TiCl4 (Ferrini et al, 1992), or with ammonium titanyl oxalate... [Pg.291]

A different approach to the substitution of metal atoms into the framework is the secondary synthesis or post-synthesis method. This is particularly effective in synthesizing metallosilicates that are difficult to crystallize from the gels containing other metal atoms or hardly incorporate metal atoms by the direct synthesis method. Substitution of Ti for A1 goes back to the 1980s. The reaction of zeolites with an aqueous solution of ammonium fluoride salts ofTi or Fe under relatively mild conditions yields materials that are dealuminated and contain substantial amounts of either iron or titanium and are essentially free of defects [58]. However, no sufficient evidence for the Ti incorporation has been provided. [Pg.137]

Symyx entered this competition in 1997 in collaboration with Hoechst with the goal of creating and validating primary and secondary synthesis and screening technologies and the use of this workflow to broadly explore mixed metal oxide compositions so as to discover and optimize new hits . The initial goal was a 10-fold increase in the space-time yield relative to the state-of-the-art MoVNb system for the ethane oxidative dehydrogenation reaction to ethylene. [Pg.7]

Structural and compositional characterization of high surface-area catalysts is crucial for evaluating whether the secondary synthesis of a particular electrocatalyst was successful. Similar to the primary screening workflow, XRD is used for the structural characterization of catalyst powders, while SEM/EDX is employed for the compositional characterization of electrocatalyst powders before and after electrochemical screening. [Pg.284]

Humic substances account for various definitions according to different authors, and also its definition changes in literature through the years. These substances are conventionally defined as a series of relatively high-molecular-weight, yellow-to black-coloured substances, formed by secondary synthesis reactions (Stevenson, 1982 Soil Science Society of America, 1996) or as a category of naturally occurring,... [Pg.306]

We report (i) isomorphous substitution of boron, by secondary synthesis, into silicalite and into highly siliceous (Si/Al>400) ZSM-5 and (ii) an improved direct synthesis of zeolite (Si,B) -ZSM-5. The chemical status of B in die boronated products depends upon reaction conditions. Careful control of the concentration of the base, the borate species and of die duration of treatment, allows the preparation of samples containing only 4-coordinated B or a mixture of 3- and 4-coordinated B in various relative concentrations. The products were characterized by magic-angle-spinning (MAS) NMR and infrared (IR) spectroscopies and by powder x-ray diffraction (XRD). [Pg.393]

The reaction of zeolites with an aqueous fluorosilicate solution under relatively mild conditions has been shown to yield zeolites with silicon enriched frameworks which are essentially free of structural defects (1). As a result of the treatment, the framework topologies of the respective zeolites are relatively unchanged, but the zeolite compositions which are produced either do not occur naturally or are not synthesized directly. The fluorosi1icate treatment process has been termed "Secondary Synthesis". [Pg.420]

The desire to synthesize molecular sieve compositions containing other than the typical silicon and aluminum atoms is evidenced by the large number of efforts, primarily in the primary synthesis area. The Secondary Synthesis process has now been extended to include substitution of both Fe3t and T1 + into the frameworks of a number of zeolites. This paper will describe substitution of iron or titanium ions into the frameworks of zeolites Y, L, W, mordenite, ZSM-5 and LZ-202. Zeolites Y, L, W and mordenite were obtained from Union Carbide Corporation. Zeolon, a synthetic mordenite, was obtained from The Norton Company. ZSM-5 was synthesized according to the procedures described by Argauer et al., (8). LZ-202 is an omega type zeolite, synthesized without the... [Pg.421]

It is clearly desirable to be able to alter the Si/Al ratio of the framework, particularly in the case of zeolites X, Y and ZSM-5. This can be conveniently achieved by "secondary synthesis", i.e. by isomorphous substitution of Si or A1 on the tetrahedral sites after the completion of the original zeolite crystallization (1-4). We shall demonstrate that ... [Pg.448]

HAMDAN AND KLINOWSKI Secondary Synthesis of Faujasitic Catalysts 449... [Pg.449]


See other pages where Synthesis secondary is mentioned: [Pg.168]    [Pg.247]    [Pg.114]    [Pg.18]    [Pg.72]    [Pg.73]    [Pg.537]    [Pg.543]    [Pg.361]    [Pg.290]    [Pg.291]    [Pg.311]    [Pg.68]    [Pg.74]    [Pg.75]    [Pg.76]    [Pg.274]    [Pg.29]    [Pg.385]    [Pg.401]    [Pg.434]    [Pg.448]    [Pg.451]   
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See also in sourсe #XX -- [ Pg.7 , Pg.607 ]




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Esters synthesis secondary alcohols

Ether synthesis from secondary alcohols

Faujasitic catalysts, secondary synthesis

Fischer-Tropsch synthesis primary product secondary reactions

Grignard synthesis of a secondary alcohol

Microbial synthesis of secondary metabolites

New approaches to the synthesis of secondary metabolites

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Secondary alcohol synthesis

Secondary alcohols synthesis, sodium borohydride

Secondary alkyl halides synthesis

Secondary amides synthesis from acid chlorides

Secondary amides, synthesis

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Secondary amines hydroxylamine synthesis

Secondary amines synthesis

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Secondary diamond synthesis

Secondary enamines synthesis

Secondary metabolites microbial synthesis

Secondary radicals synthesis

Secondary synthesis of faujasitic catalysts

Secondary synthesis process, description

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