Zeolite earths

The tetrahydropyranyl ether, prepared from a phenol and dihydropyran (HCl/EtOAc, 25°, 24 h) is cleaved by aqueous oxalic acid (MeOH, 50-90°, 1-2 h). Tonsil, Mexican Bentonite earth, HSZ Zeolite, and H3[PW,204o] have also been used for the tetrahydropyranylation of phenols. The use of [Ru(ACN)3(triphos)](OTf)2 in acetone selectively removes the THP group from a phenol in the presence of an alkyl THP group. Ketals of acetophenones are also cleaved. ... 

The structural complexity of the 3D framework aluminosilicates precludes a detailed treatment here, but many of the minerals are of paramount importance. The group includes the feldspars (which are the most abundant of all minerals, and comprise 60% of the earth s crust), the zeolites (which find major applications as molecular sieves, desiccants, ion exchangers and water softeners), and the ultramarines which, as their name implies, often have an intense blue colour. All are constructed from Si04 units in which each O atom is shared by 2 tetrahedra (as in the various forms of Si02 itself), but up to one-half of the Si... 

The alumina content, the amount of rare-earth, and the type and amount of zeolite affect catalyst tolerance to vanadium poisoning. 

Alkaline earth metals in general, and sodium in particular, are detrimental to the FCC catalyst. Sodium permanently deactivates the catalyst by neutralizing its acid sites. In the regenerator it causes the zeolite to collapse, particularly in the presence of vanadium. Sodium comes from two prime sources ... 

Until the late 1970s, the NaY zeolite was mostly ion exchanged with rare earth components. Rare earth components, such as lanthanum and... 

Zeolites with lower UCS are initially less active than the conventional rare earth exchanged zeolites (Figure 3-5). However, the lower UCS zeolites tend to retain a greater fraction of their activity under severe thermal and hydrothermal treatments, hence the name ultrastable Y. 

A freshly manufactured zeolite has a relatively high UCS in the range of 24.50°A to 24.75°A. The thermal and hydrothermal environment of the regenerator extracts alumina from the zeolite structure and, therefore, reduces its UCS. The final UCS level depends on the rare earth and sodium level of the zeolite. The lower the sodium and rare earth content of the fresh zeolite, the lower UCS of the equilibrium catalyst (E-cat). 

Rare Earth Level. Rare earth (RE) elements serve as a bridge to stabilize aluminum atoms in the zeolite structure. They prevent the... 

A fully rare-earth-exchanged zeolite equilibrates at a high UCS. whereas a non-rare-earth zeolite equilibrates at a very low UCS in the range of 24.25 [3]. All intermediate levels of rare-earth-exchanged zeolite can be produced. The rare earth increases zeolite activity and... 

Figure 3-5. Comparison of activity retention between rare-earth-exchanged zeolites versus USY zeolites. (Source Grace Davison Octane Handbook.)...

UCS, rare earth, and sodium are just three of the parameters that are readily available to characterize the zeolite properties. They provide valuable information about catalyst behavior in the cat cracker. If required, additional tests can be conducted to examine other zeolite properties. 

A typical NaY zeolite contains approximately 13 wt% Na20. To enhance activity and thermal and hydrothermal stability of NaY, the sodium level must be reduced. This is normally done by the ion exchanging of NaY with a medium containing rare earth cations and/ or hydrogen ions. Ammonium sulfate solutions are frequently employed as a source for hydrogen ions. 

At this state of the catalyst synthesis there are two approaches for further treamient of NaY. Depending on the particular catalyst and the catalyst supplier, further treatment (rare earth exchanged) of NaY can be accomplished either before or after its incorporation into the matrix. Post-treatment of the NaY zeolite is simpler, but may reduce ion exchange efficiency. 

A rare-earth-exchanged zeolite increases hydrogen transfer reactions. In simple terms, rare earth forms bridges between two to three acid sites in the catalyst framework. In doing so, the rare earth protects... 

Rare Earth. Increasing the amount of rare earth oxide (REO) on the zeolite decreases the octane (Figure 6-5). 

Rare Earth is a generic name used for the 14 metallic elements of the lanthanide series used in the manufacturing of FCC catalyst to improve stability, activity, and gasoline selectivity of the zeolite. 

Zeolites are naturally occurring hydrous aluminum-sodium silicates in porous granule form. They are capable of exchanging their sodium base for calcium or magnesium and of expelling these alkaline earth metals for sodium by treatment with salt. Thus, they are a type of ion-exchange media. (Some zeolites act as molecular sieves by adsorption of water and polar compounds.)... 

Kwak, J.H., Szanyi, J. and Peden, C.H.F. (2004) Non-thermal plasma-assisted NOx reduction over alkali and alkaline earth ion exchanged Y, FAU zeolites, Catal. Today 89, 135—41. 

This is a quite remarkable result, as the chemoselective hydrogenation of geraniol over a heterogeneous catalyst has rarely been reported. It can be carried out over platinum containing zeolite (9), over Pt/Al203 modified with carboxylic acids (10), over Ni/diatomaceous earth and alkali hydroxides or carbonates (11) or NiRaney and alkali or alkaline earth metal hydroxides (12), yields never exceeding 85%. 

Fig. 28. The ESR spectra of Or on - -irradiated alkaline earth zeolites. Only the low-field maxima are shown here 110).

Di or trivalent cations are able to induce the dissociation of coordinated water molecules to produce acidic species such as MOH+ (or MOH2+ for trivalent metal cations) and H+. Several infrared studies concerning rare-earth or alkali-earth metal cation exchanged Y zeolites have demonstrated the existence of such species (MOH+ or MOH2+) [3, 4, 5, 6]. However, the literature is relatively poor concerning the IR characterization of these acidic sites for LTA zeolites. The aim of the present work is to characterize 5A zeolite acidity by different techniques and adsorption tests carried on 5A zeolite samples with different ion exchange. 

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