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Well-type Reactors

Being in a way the link between pellet-type reactors and well-type reactors, Klein et al. presented a multiple-bead reactor [74] in combination with a split and pool synthesis. The reactor shown in Figure 3.43 consists of pellet-type catalyst carriers, so-called beads, which are positioned in square containers. [Pg.452]

This reaction has been studied using batch reactors, perfectly stirred continuous reactors, tubular continuous reactors, BENSON type reactors, wall-less reactors and shock tubes. The reaction has been carried out at temperatures between 700 and 1300 K, at pressures of 0.1 Pa to 10 Pa and at reaction times of 10 s to 10 s. The effects of the nature and of the area of the reactor walls as well as those of various additives have also been studied. The diversity of the studies carried out by a dozen teams throughout the world, the particularly widespread range of operating conditions (600 K for the temperature, which represents 11 orders of magnitude for the rate of initiation, 8 orders of magnitude for the pressure and reaction duration) make the pyrolysis of neopentane into a model radical reaction. [Pg.171]

The sample pre-treatment as well as adsorption and desorption experiments were performed with a flow rate of 100 cm rnin-i that was passed through a quartz reactor (U-type) containing 1 g of bentonite meshes. The sample was first pre-treated under N2 flow at 473 K for 30 minutes than adsorption was carried out using the model mixture flow until saturation was reached in order to obtain breakthrough curves. The gas mixture was switched again to pure N2 flow, to proceed with isothermal desorption xmtil o-xylene concentration at the reactor outlet reached zero. This step was followed by a subsequent linear heating in order to perform Temperature Programmed Desorption (TPD) experiment. [Pg.423]

Basic technologies of a vessel-type pressurized water reactor, well proven through worldwide operation experience ... [Pg.221]

Some characteristics of the MARS design are similar to well-known PWRs (primary loop type, core geometry and materials, reactor control type, etc.). Along with them, the MARS design incorporates the following innovative solutions ... [Pg.166]

In fact, it is often possible with stirred-tank reactors to come close to the idealized well-stirred model in practice, providing the fluid phase is not too viscous. Such reactors should be avoided for some types of parallel reaction systems (see Fig. 2.2) and for all systems in which byproduct formation is via series reactions. [Pg.53]

The selection of a particular type of reduction depends on technical feasibiUty and the economics of the process as well as on physicochemical considerations. In particular, the reducing agent should be inexpensive relative to the value of the metal to be reduced. The product of the reaction, RX, should be easily separated from the metal, easily contained, and safely recycled or disposed of. Furthermore, the physical conditions for the reaction should be such that a suitable reactor can be designed and operated economically. [Pg.164]

MAO is a relatively expensive chemical its price in 1994 was about 450/kg of 30 wt % MAO solution, but projected to decrease to about 200/kg (28). Continuous efforts to replace MAO have resulted in the development of co-catalysts containing mixtures of MAO and trimethyl aluminum (29) as well as new co-catalyst types (30,31). Another approach is to prepare MAO directiy in a polymeriza tion reactor by co-feeding into it trimethyl aluminum and water (32). [Pg.398]

The second type of solution polymerization concept uses mixtures of supercritical ethylene and molten PE as the medium for ethylene polymerization. Some reactors previously used for free-radical ethylene polymerization in supercritical ethylene at high pressure (see Olefin POLYMERS,LOW DENSITY polyethylene) were converted for the catalytic synthesis of LLDPE. Both stirred and tubular autoclaves operating at 30—200 MPa (4,500—30,000 psig) and 170—350°C can also be used for this purpose. Residence times in these reactors are short, from 1 to 5 minutes. Three types of catalysts are used in these processes. The first type includes pseudo-homogeneous Ziegler catalysts. In this case, all catalyst components are introduced into a reactor as hquids or solutions but form soHd catalysts when combined in the reactor. Examples of such catalysts include titanium tetrachloride as well as its mixtures with vanadium oxytrichloride and a trialkyl aluminum compound (53,54). The second type of catalysts are soHd Ziegler catalysts (55). Both of these catalysts produce compositionaHy nonuniform LLDPE resins. Exxon Chemical Company uses a third type of catalysts, metallocene catalysts, in a similar solution process to produce uniformly branched ethylene copolymers with 1-butene and 1-hexene called Exact resins (56). [Pg.400]

Flow Reactors Fast reactions and those in the gas phase are generally done in tubular flow reaclors, just as they are often done on the commercial scale. Some heterogeneous reactors are shown in Fig. 23-29 the item in Fig. 23-29g is suited to liquid/liquid as well as gas/liquid. Stirred tanks, bubble and packed towers, and other commercial types are also used. The operadon of such units can sometimes be predicted from independent data of chemical and mass transfer rates, correlations of interfacial areas, droplet sizes, and other data. [Pg.708]

The Fischer-Tropsch reaction is highly exothermic. Therefore, adequate heat removal is critical. High temperatures residt in high yields of methane, as well as coking and sintering of the catalyst. Three types of reac tors (tubular fixed bed, fluidized bed, and slurry) provide good temperature control, and all three types are being used for synthesis gas conversion. The first plants used tubular or plate-type fixed-bed reactors. Later, SASOL, in South Africa, used fluidized-bed reactors, and most recently, slurry reactors have come into use. [Pg.2377]

The most reliable recycle reactors are those with a centrifugal pump, a fixed bed of catalyst, and a well-defined and forced flow path through the catalyst bed. Some of those shown on the two bottom rows in Jankowski s papers are of this type. From these, large diameter and/or high speed blowers are needed to generate high pressure increase and only small gaps can be tolerated between catalyst basket and blower, to minimize internal back flow. [Pg.60]


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See also in sourсe #XX -- [ Pg.98 ]




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