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Catalyst continued particles

A reasonable throughput screening equipment consisting of six parallel reactor tubes was constructed. The system operates continuously and can be used for screening of various catalysts, different particle sizes and temperatures. Gas, gas-sohd and gas-solid-liquid applications are possible. The screening equipment is coupled to gas chromatographic-mass spectrometric analysis. The constraction principles, the equipment as well as the application of the equipment is demonstrated with three-phase catalytic systems. [Pg.419]

PtMo alloys are not as effective as PtRu for methanol, or ethanol, oxidation. As shown in Figure 29, the d band vacancy per Pt atom for the PtMo/C catalyst continues to increase until 0.6 V vs RHE, in contrast to the behavior of PtRu/C. ° The authors attribute this difference to the lack of removal of the Cl fragments from the particle surface by the oxy-hydroxides of Mo. However, the difference in the electrocatalytic activity of PtRu and PtMo catalysts may be attributed to ensemble effects as well as electronic effects. The former are not probed in the white line analysis presented by Mukerjee and co-workers. In the case of methanol oxidation, en-... [Pg.391]

This case study is concerned with a three-phase gas-liquid-solid (catalytic) reaction. A systematic stepwise procedure has been described for determining the rate-controlling step, which depends on the catalyst type, particle size, operating pressure and temperature, mass transfer coefficient, and concentrations of reactants and products. As indicated, the rate-controlling step may change with location in a continuous reactor and with time in a batch reactor. [Pg.943]

Commercial eoordination catalysts (except the homogeneous metalloeene/aluminoxane eatalysts) are heterogeneous solids. During the polymerization the catalyst particles eonvert from pure catalyst to catalyst+polymer particles by a repliealion ptoeess [20]. The overall shape of the parliele is maintained as the polymerization continues. The ehaiacteristics of the final polymer parliele are... [Pg.240]

When a continuous particle feeding of a CFB is cut off, particles become dilute and well distributed in the bed. Because of the low solids holdup and short residence time, this bed can only be used in pneumatic conveying, or in particular chemical reactors, where the reaction rate is very high or extra active catalyst is used. All internals used in risers can be applied in this situation, so it will not be discussed here. [Pg.184]

Okubo et al successfully achieved an aqueous microsuspension RTCP of MMA with NIS catalyst. The particle phase included MMA (8 M), CP-I (80mM), AIBN (lOmM), and NIS (ImM), as in the mentioned bulk polymerization (Table 7.1 (entry 11)). The water content was 90% with the use of a cationic surfactant, dodecyltrimethyl ammonium bromide. The polymerization smoothly proceeded and the conversion reached 93% for 2 h at 80 °C. The PDI was small (1.3-1.5) throughout the polymerization, demonstrating the successful polymerization in water continuous phase. [Pg.280]

In addition to the advantage of high heat transfer rates, fluidized beds are also useful in situations where catalyst particles need frequent regeneration. Under these circumstances, particles can be removed continuously from the bed, regenerated, and recycled back to the bed. In exothermic reactions, the recycling of catalyst can be... [Pg.58]

Macroscopic properties often influence tlie perfoniiance of solid catalysts, which are used in reactors tliat may simply be tubes packed witli catalyst in tlie fonii of particles—chosen because gases or liquids flow tlirough a bed of tliem (usually continuously) witli little resistance (little pressure drop). Catalysts in tlie fonii of honeycombs (monolitlis) are used in automobile exliaust systems so tliat a stream of reactant gases flows witli little resistance tlirough tlie channels and heat from tlie exotlieniiic reactions (e.g., CO oxidation to CO,) is rapidly removed. [Pg.2701]

Some slurry processes use continuous stirred tank reactors and relatively heavy solvents (57) these ate employed by such companies as Hoechst, Montedison, Mitsubishi, Dow, and Nissan. In the Hoechst process (Eig. 4), hexane is used as the diluent. Reactors usually operate at 80—90°C and a total pressure of 1—3 MPa (10—30 psi). The solvent, ethylene, catalyst components, and hydrogen are all continuously fed into the reactor. The residence time of catalyst particles in the reactor is two to three hours. The polymer slurry may be transferred into a smaller reactor for post-polymerization. In most cases, molecular weight of polymer is controlled by the addition of hydrogen to both reactors. After the slurry exits the second reactor, the total charge is separated by a centrifuge into a Hquid stream and soHd polymer. The solvent is then steam-stripped from wet polymer, purified, and returned to the main reactor the wet polymer is dried and pelletized. Variations of this process are widely used throughout the world. [Pg.384]

In the slurry process, the hydrolysis is accompHshed using two stirred-tank reactors in series (266). Solutions of poly(vinyl acetate) and catalyst are continuously added to the first reactor, where 90% of the conversion occur, and then transferred to the second reactor to reach hiU conversion. Alkyl acetate and alcohols are continuously distilled off in order to drive the equiUbrium of the reaction. The resulting poly(vinyl alcohol) particles tend to be very fine, resulting in a dusty product. The process has been modified to yield a less dusty product through process changes (267,268) and the use of additives (269). Partially hydroly2ed products having a narrow hydrolysis distribution cannot be prepared by this method. [Pg.485]

GLS Fluidized with a Stable Level of Catalyst Only the fluid mixture leaves the vessel. Gas and liquid enter at the bottom. Liquid is continuous, gas is dispersed. Particles are larger than in bubble columns, 0.2 to 1.0 mm (0.008 to 0.04 in). Bed expansion is small. Bed temperatures are uniform within 2°C (3.6°F) in medium-size beds, and neat transfer to embedded surfaces is excellent. Catalyst may be bled off and replenished continuously, or reactivated continuously. Figure 23-40 shows such a unit. [Pg.2120]


See other pages where Catalyst continued particles is mentioned: [Pg.524]    [Pg.31]    [Pg.154]    [Pg.359]    [Pg.182]    [Pg.62]    [Pg.31]    [Pg.246]    [Pg.665]    [Pg.355]    [Pg.186]    [Pg.194]    [Pg.1969]    [Pg.4562]    [Pg.198]    [Pg.79]    [Pg.402]    [Pg.826]    [Pg.69]    [Pg.325]    [Pg.535]    [Pg.1859]    [Pg.883]    [Pg.72]    [Pg.384]    [Pg.385]    [Pg.386]    [Pg.399]    [Pg.491]    [Pg.6]    [Pg.482]    [Pg.52]    [Pg.464]    [Pg.173]    [Pg.181]    [Pg.222]    [Pg.509]    [Pg.514]   
See also in sourсe #XX -- [ Pg.417 ]




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Catalyst [continued)

Catalyst particles

Particle continued)

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