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Mobil process

A second Mobil process is the Mobil s Vapor Phase Isomerization Process (MVPI) (125,126). This process was introduced in 1973. Based on information in the patent Hterature (125), the catalyst used in this process is beHeved to be composed of NiHZSM-5 with an alumina binder. The primary mechanism of EB conversion is the disproportionation of two molecules of EB to one molecule of benzene and one molecule of diethylbenzene. EB conversion is about 25—40%, with xylene losses of 2.5—4%. PX is produced at concentration levels of 102—104% of equiHbrium. Temperatures are in the range of 315—370°C, pressure is generally 1480 kPa, the H2/hydrocatbon molar ratio is about 6 1, and WHSV is dependent on temperature, but is in the range of 2—50, although normally it is 5—10. [Pg.422]

Volcanic activity has a significant effect on the mobilization of metals, particularly the more volatile ones, e.g., Pb, Cd, As, and FFg. Effects of volcanism are qualitatively different from those of the weathering and other near-surface mobilization processes mentioned above, in that volcanism transports materials from much deeper in the crust and may inject elements into the atmospheric reservoir. [Pg.378]

Most mechanistic work has focused on chemical reactions in solution or extremely simple processes in the gas phase. There is increasing interest in reactions in solids or on solid surfaces, such as the surfaces of solid catalysts in contact with reacting gases. Some such catalysts act inside pores of defined size, such as those in zeolites. In these cases only certain molecules can penetrate the pores to get to the reactive surface, and they are held in defined positions when they react. In fact, the Mobil process for converting methanol to gasoline depends on zeolite-catalyzed reactions. [Pg.52]

The elements deposited within the sediment matrix show that mobilization processes may be occurring in the upper layers. At Station SIN 3, figure 4d for example, the element deposited (pg-cm-2) in the topmost layers decreases, often much more than in the concentration (Mg g 1). This may be due to organic matter decomposition and/or to environmental chemical reactions of solubility and precipitation of the given element. The metal must have been removed rapidly from the water column since the sediment concentration is shown to decrease rapidly with distance from the shipyard (Stations SIN 3 and SIN 2). Lead may not be mobilized significantly after deposition since any diffusion in the pore water would tend to "smooth" the concentration profile with time. [Pg.339]

MTA [Methanol to aromatics] A common abbreviation for any process which achieves this conversion, notably a Mobil process. [Pg.185]

MTG [Methanol to gasoline] A common abbreviation for any process achieving this conversion, notably the Mobil process. This uses as a catalyst the synthetic zeolite ZSM-5, invented at the Mobil Research Laboratory in 1972. The process was first disclosed in 1976 and commercialized in 1985 by New Zealand Synfuels, a joint venture of Mobil Corporation and Petrocorp. In 1990, this process was providing one third of New Zealand s gasoline requirements. [Pg.185]

Proteins or antibodies (36 pg) were mixed with ampholine pH 3.5—9.5 (final concentration of 5%, Amersham Biosciences, distributed by GE Healthcare, Uppsala, Sweden), p7 markers (Bio-Rad, Hercules, CA), and hydroxypropyl methyl cellulose (final concentration of 0.2% HPMC, Sigma-Aldrich, St. Louis, MO). The final protein concentration was 0.3mg/mL. Figure 17 shows a schematic of the sample preparation. The mixture was mixed thoroughly and was introduced to the capillary (eCAP neutral-coated, 50 micron X 30 cm, Beckman, Fullerton, CA) by hydrodynamic injection. Injections were performed using 20 psi for 99 s. The solution was then separated under an electric field of 25 kV for 10 min. The focused protein was then pushed/pulled out of the capillary through a mobilization process using the cathodic mobilizer (Bio-Rad, Hercules, CA). [Pg.373]

Cost Is about 10-12/GJ for both methanol and synthetic gasoline for transportation usage. The additional conversion costs of methanol to gasoline by the Mobil process roughly balance the distribution and usage costs of methanol/gasoline blends. [Pg.159]

The incremental cost of using methanol in gasoline is approximately equal to the incremental cost of converting the methanol to gasoline by the Mobil process. Such end-use costs must of course be included in overall fuel comparisons. [Pg.160]

According to the vendor, the ISOCELL technology can provide in a frustum-shaped block of preselected size the complete isolation and removal of radioactive materials from in situ site conditions. The technology uses lifting and/or glazing to keep wastes contained inside the frozen blocks and to reduce dust and aerosol releases during lifting and mobilization processes. [Pg.926]

Parsippany, NJ, 07054, USA Mobile Process Technology, 2070 Airways Boulevard, Memphis,... [Pg.493]

A special thanks to Mobile Process Technology for pilot scale testing of Deloxan THP II and MP metal scavengers. [Pg.499]

The Mobil process as discussed still uses syngas in its initial step. Olah has shown,79 however, that it is possible to convert methane directly by selective electrophilic halogenation to methyl halides and through their hydrolysis to methyl alcohol [Eq. (1.12)]. When bromine is used, the HBr byproduct of the reaction is readily reoxidized to bromine, allowing a catalytic process in which bromine acts only as a redox catalyst [Eq. (1.13)] ... [Pg.16]

Both the Fischer-Tropsch reaction and the Mobil process enable one to convert synthesis gas into hydrocarbons. Since synthesis gas may be obtained from coal, we have in effect a means of converting coal u> gasoline. Geimany moved its Panzer Korps in World War II with synthetic fuels made from (he Fischer-Tropsch reaction, and improved technological developments have enhanced the attractiveness of the process. South African Synthetic Oil Limiied fSASOLJ currently operates several modern Fischer-Tropsch plants. Many organometallic chemists refer to both the Fischer-Tropsch and Mobil processes as political processes 1 2 because they are heavily subsidized by countries that find it important to be independent of foreign oil. [Pg.894]

Anawar, H.M., Akai, J., Komaki, K. et al. (2003) Geochemical occurrence of arsenic in groundwater of Bangladesh Sources and mobilization processes. Journal of Geochemical Exploration, 77(2-3), 109-31. [Pg.199]

Acharyya, S.K. (2002) Arsenic contamination in groundwater affecting major parts of southern West Bengal and parts of western Chhattisgarh source and mobilization process. Current Science, 82(6), 740-44. [Pg.339]

Methanol to Gasoline—The Mobil Process. Mobil Research and Development Corporation developed a process that catalytically dehydrates and polymerizes methanol to produce a high octane unleaded gasoline. The catalyst is one of a new family of synthetic zeolites designated ZSM-5 by Mobil. These new zeolites have a unique channel structure, different from previously known wide-pore (9-10 A in diam-... [Pg.898]

This is an important industrial reaction, alone or in combination with others. The CH3OH production is often coupled to oxidation to formaldehyde, methanol to gasoline (Mobil) process, methanol to olefins process, carbonylation, etc. Due to this, a large volume of information already exists on catalyst preparation, kinetics, reactors and all other aspects of the related chemical technology [53]. However, let us concentrate our attention here on just one selected problem the role of the promoter and the nature of the active site on the metal on oxides catalysts. Let us mention in passing that pure metals (promoter free) most likely do not catalyze the synthesis. [Pg.174]

Adaptation of existing experimental methods and theories, and development of new ones, to study (usually at reservoir conditions) the key phase, dispersion, and interfacial properties that control dispersion-based mobility processes, as determined from pore-level mechanisms and from other studies (D. H. Smith, Southwest American Chemical Society Meeting, Houston, November 19-21, 1986). [Pg.12]


See other pages where Mobil process is mentioned: [Pg.135]    [Pg.543]    [Pg.552]    [Pg.553]    [Pg.68]    [Pg.60]    [Pg.8]    [Pg.541]    [Pg.47]    [Pg.299]    [Pg.313]    [Pg.47]    [Pg.59]    [Pg.67]    [Pg.192]    [Pg.154]    [Pg.67]    [Pg.894]    [Pg.126]   
See also in sourсe #XX -- [ Pg.164 , Pg.201 ]

See also in sourсe #XX -- [ Pg.646 ]




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Drift mobility process

Fuel processing systems mobile

Industrial processes Mobil-Badger process

Mass transport processes mobile phase

Mobil Badger process, zeolite catalysts

Mobil MTG process

Mobil Selective Dewaxing process, zeolite catalysts

Mobil process poly

Mobil-Badger process

Mobil/Badger cumene process

Mobile phase solvation processes

Mobility factors/processes

Personalized mobile information processing

Practical Fuel Processing - Mobile Applications

Processes Mobil Badger ethylbenzene

Processes Mobil selective dewaxing

Xylenes Mobil xylene isomerization process

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