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Mordenite

Free apertures in second channel system are too small for organic molecules to diffuse readily, making the channel system of mordenite essentially monodimensional. [Pg.2781]

Zeolites are tire product of a hydrotliennal conversion process [28]. As such tliey can be found in sedimentary deposits especially in areas tliat show signs of fonner volcanic activity. There are about 40 naturally occurring zeolite types. Types such as chabazite, clinoptilolite, mordenite and phillipsite occur witli up to 80% phase purity in quite large... [Pg.2783]

Nearly all commercial acetylations are realized using acid catalysts. Catalytic acetylation of alcohols can be carried out using mineral acids, eg, perchloric acid [7601-90-3], phosphoric acid [7664-38-2], sulfuric acid [7664-93-9], benzenesulfonic acid [98-11-3], or methanesulfonic acid [75-75-2], as the catalyst. Certain acid-reacting ion-exchange resins may also be used, but these tend to decompose in hot acetic acid. Mordenite [12445-20-4], a decationized Y-zeohte, is a useful acetylation catalyst (28) and aluminum chloride [7446-70-0], catalyzes / -butanol [71-36-3] acetylation (29). [Pg.66]

Mordenite H+ HJ(A103)3(S03)J 12-ring (free) 0.70 trapping of Kr from nuclear off-gas... [Pg.254]

Fig. 3. Model of the crystal structure of the mineral mordenite showing the main channel formed by 12-membered ring and small channels which contain some of the sodium cations. Synthetic types of mordenite exhibit the adsorption behavior of a 12-membered ring, whereas the mineral does not, probably... Fig. 3. Model of the crystal structure of the mineral mordenite showing the main channel formed by 12-membered ring and small channels which contain some of the sodium cations. Synthetic types of mordenite exhibit the adsorption behavior of a 12-membered ring, whereas the mineral does not, probably...
The presence of an electron donor causes the equiHbrium to shift to the left. The acidity represented by this mechanism is important in hydrocarbon conversion reactions. Acidity may also be introduced in certain high siHca zeoHtes, eg, mordenite, by hydrogen-ion exchange, or by hydrolysis of a zeoHte containing multivalent cations during dehydration, eg,... [Pg.449]

The zeoHtes used for catalysis are principally modified forms of zeoHte Y, acid forms of synthetic mordenite, and ZSM-5. [Pg.449]

All 2eohte types are available as powders unless otherwise indicated. Chaba2ite and Mordenite, smaU-pore are available as extmdates only. [Pg.455]

Catalytic dewaxiag (32) is a hydrocrackiag process operated at elevated temperatures (280—400°C) and pressures, 2,070—10,350 kPa (300—1500 psi). However, the conditions for a specific dewaxiag operatioa depead oa the aature of the feedstock and the product pour poiat required. The catalyst employed for the process is a mordenite-type catalyst that has the correct pore stmcture to be selective for normal paraffin cracking. Platinum on the catalyst serves to hydrogenate the reactive iatermediates so that further paraffin degradation is limited to the initial thermal reactions. [Pg.212]

Polynuclear Aromatics. The alkylation of polynuclear aromatics with olefins and olefin-producing reagents is effected by acid catalysts. The alkylated products are more compHcated than are those produced by the alkylation of benzene because polynuclear aromatics have more than one position for substitution. For instance, the alkylation of naphthalene [91-20-3] with methanol over mordenite and Y-type zeoHtes at 400—450°C produces 1-methylnaphthalene [90-12-0] and 2-methylnaphthalene at a 2-/1- ratio of about 1.8. The selectivity to 2-methylnaphthalene [91-57-6] is increased by applying a ZSM-5 catalyst to give a 2-/1- ratio of about 8 (102). [Pg.53]

Ca.ta.lysts, A small amount of quinoline promotes the formation of rigid foams (qv) from diols and unsaturated dicarboxyhc acids (100). Acrolein and methacrolein 1,4-addition polymerisation is catalysed by lithium complexes of quinoline (101). Organic bases, including quinoline, promote the dehydrogenation of unbranched alkanes to unbranched alkenes using platinum on sodium mordenite (102). The peracetic acid epoxidation of a wide range of alkenes is catalysed by 8-hydroxyquinoline (103). Hydroformylation catalysts have been improved using 2-quinolone [59-31-4] (104) (see Catalysis). [Pg.394]

Adsorbents Table 16-3 classifies common adsorbents by structure type and water adsorption characteristics. Structured adsorbents take advantage of their crystalline structure (zeolites and sllicalite) and/or their molecular sieving properties. The hydrophobic (nonpolar surface) or hydrophihc (polar surface) character may vary depending on the competing adsorbate. A large number of zeolites have been identified, and these include both synthetic and naturally occurring (e.g., mordenite and chabazite) varieties. [Pg.1500]

For cumene production (from benzene and propene) a new process has been developed in which H-mordenite (with high Si/Al) serves as the catalyst. Here the... [Pg.209]


See other pages where Mordenite is mentioned: [Pg.2780]    [Pg.2781]    [Pg.2783]    [Pg.2791]    [Pg.188]    [Pg.311]    [Pg.421]    [Pg.281]    [Pg.281]    [Pg.282]    [Pg.285]    [Pg.292]    [Pg.293]    [Pg.443]    [Pg.444]    [Pg.445]    [Pg.446]    [Pg.449]    [Pg.449]    [Pg.451]    [Pg.452]    [Pg.455]    [Pg.455]    [Pg.365]    [Pg.178]    [Pg.196]    [Pg.201]    [Pg.201]    [Pg.1500]    [Pg.1501]    [Pg.1541]    [Pg.1543]    [Pg.1547]    [Pg.163]    [Pg.87]    [Pg.334]    [Pg.337]    [Pg.148]   
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Acid-leached mordenites

Adsorbents mordenite

Alkylation with Other Alkenes over H-Mordenite

Alumina mordenite

Aluminum deficient H-mordenite

Aluminum-deficient large-port mordenites

Aluminum-deficient mordenite

Aluminum-deficient mordenite acid properties

Aluminum-deficient mordenite catalytic properties

Boron-substituted mordenites

Catalyst fluorided mordenite

Catalyst supports mordenite

Catalysts H mordenite

Channels mordenite

Crystallization mordenite

Cu-mordenite

Dealuminated mordenite, toluene

Electron diffraction patterns mordenite crystals

Exchanged zeolites mordenite

Extracted H-mordenite

Fluorided mordenite

Framework of mordenite

H-Mordenite Deactivation during the SCR of NOx. Adsorption and

H-Mordenite, acidity

H-mordenite

H-mordenites

High-silica mordenite, preparation

Hydrogen into mordenite

Hydrogen mordenite

Hydrogen mordenites

Iron mordenites

Isomerization mordenite supports

Isopropylation over H-Mordenite

Methane mordenite

Modified framework structures mordenites

Montmorillonite Mordenite zeolite

Mordenite (MOR)

Mordenite Subject

Mordenite acetal formation

Mordenite acid properties

Mordenite acid-base properties

Mordenite acid-leached

Mordenite adsorption

Mordenite band assignments

Mordenite bifunctional catalysts

Mordenite catalyst

Mordenite catalyst pore size

Mordenite catalysts based

Mordenite composition

Mordenite crystals

Mordenite dealuminated

Mordenite dealumination

Mordenite dehydrated form

Mordenite disproportionation

Mordenite dual function catalysts based

Mordenite esterifications

Mordenite ether formations

Mordenite extracted

Mordenite framework

Mordenite framework structure

Mordenite large-port

Mordenite mechanism

Mordenite membranes

Mordenite metal cations

Mordenite nitrations

Mordenite pore structure

Mordenite preparation

Mordenite sheets

Mordenite sorption

Mordenite stability

Mordenite steam-acid leaching

Mordenite synthesis

Mordenite synthetic

Mordenite toluene disproportionation

Mordenite zeolites, framework structures related

Mordenite, cesium-exchanged

Mordenite, large crystals

Mordenite, structure

Mordenite, surface acidity

Mordenites

Mordenites

Na-mordenite

Natural mordenite

Nitrogen adsorption by mordenite

Of dealuminated mordenite

Of mordenite

Of sodium mordenite

Palladium mordenite catalysts

Pd/mordenites

Poly encapsulated in mordenite

Pt mordenite

Shape selectivity zsm5 and mordenite

Siliceous mordenite crystals

Subject with zeolite mordenite

Synthesis of Mordenite

Synthetic mordenite, catalytic properties

Synthetic mordenites

Ti-Mordenite

Tin mordenite

Transalkylation dealuminated mordenite

Zeolite mordenite

Zeolites having mordenite-, ferrierite-, boggsite-. epistilbite-, and terranovaite-type framework

Zeolites mordenites

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