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Barton reactor

Another process, the Barton process, is based on molten lead. The core of such a device is the "Barton reactor", a heated pot that is partly filled with molten lead. It is continuously refilled by a fine stream of molten lead. Fine droplets of lead are produced by a fast rotating paddle that is partly immersed under the surface of the molten lead within the "Barton reactor". The surface of each droplet is transformed by oxidation into a shell of PbO by an airstream that simultaneously carries away the oxidized particles if they are small enough otherwise, they fall back into the melt and the process is repeated. Thus the airstream acts as a classifier for particle size. [Pg.166]

Investment costs. Barton pot systems are significantly cheaper than the ball mill equipment, which makes them strong favourites in this respect, too. The lower price, the higher productivity and the lower operating and maintenance costs of Barton reactors have lead to a boom in their application by numerous battery companies worldwide after the 1960s. [Pg.236]

The oxide exiting either the Barton or ball mill reactor is conveyed by an air stream to separating equipment, ie, settling tank, cyclone, and baghouse, after which it is stored in large hoppers or dmmmed for use in paste mixing. Purity of the lead feed stock is extremely critical because minute quantities of some impurities can either accelerate or slow the oxidation reaction markedly. Detailed discussions of the oxide-making process and product are contained in references 55—57. [Pg.576]

Comprehensive discussions on reactor stability theories and safe engineering problems were presented by Eigenberger and Schuler (1986, 1989), Zaldivar (1991), Barton and Rogers (1993), and Grewer (1994). The very basic theory developed by Semenov (1928) for zero-order reactions is very illustrative for a physical explanation of explosion phenomena. The theory enables evaluation of conditions at which thermal explosion will occur. [Pg.375]

Barton, J.A. and Nolan, P.F., 1991, in Safety in Chemical Batch Reactors and Storage Tanks , Benuzzi, A. and Zaldivar, J.M. (Eds.), Kluwer Academic Services, Dordrecht, pp. 99-124. Barton, J. and Rogers, R. (Eds.), 1993, Chemical Reaction Hazards - A Guide, Inst. Chem. Engrs., Rugby. [Pg.405]

Recently, Barton and coworkers investigated the mechanism of the 1,2-silyl migration in a related system through a combination of experiment and theory40. Pyrolysis of 12 at 600 °C cleanly produced a mixture of 12 and methylenedisilacyclopentene 13 (25%) (equation 12). A kinetic study of this reaction was conducted over the temperature range of 520-600 °C in a stirred flow reactor. The Arrehnius parameters for the first order formation of 13 were logA = 12.5 s-1 and Ea = 54 kcalmol-1. In the pyrolysis of a related all-carbon system 14, decomposition occurred at 550 °C but no isomerization to the methylene cyclopentene 15 was observed up to 700 °C (equation 13). [Pg.858]

Barton equilibrium line, or fall on the pyrite-pyrrhotite line of the phase diagrams. The coals with higher intrinsic pyrite content or those to which pyrite or iron-containing materials were added have pyrrhotites which fall nearer the reactor zone. [Pg.367]

Barton et al. (1999) briefly described their version of a plug-flow quartz capillary reactor cell. They used quartz capillaries with 0.9 mm diameter and 0.1 mm wall thickness. The heating was by a copper heat sink that was in turn heated by cartridge heaters. The quartz tube was packed with meshed particles of catalyst. [Pg.387]

Secondly, the geometric closure of nanoscopic space, either by endo-skeletal or exo-skeletal constructions, creates new surfaces and enclosures upon and where in reactions may be examined. Turro, Barton and Tomalia [40] refer to these domains, whether evolving from micelles, dendrimers or DNA, as nano-reactors". Cram has described such contained space in his carcerands as new phases of matter [41], Miller et al. [42] have used related linear nanostructures as molecular rulers which are observable as single molecular species by transmission electron miecroscope. On the other hand, Amit et al. [16] have shown that important biological events, such as the formation of antigen-antibody complexes involve nanoscopic areas of 600-1000 A2 (6-10 nm2). [Pg.209]

N 2.5-6.0 low 0-50 Free drift Crushed seized limestone Batch reactor "vigorously agitated" 0.078 3.6 Barton and Vatanatham (38)... [Pg.550]

In a second example, Ryu and co-workers [87, 88] demonstrated the nitrite photolysis (Barton reaction) of the steroidal substrate 157 to afford 158 (Scheme 6.41), a key intermediate in the synthesis of an endothelin receptor antagonist, using a 300 W high-pressure mercury lamp. Maintaining a gap of 7.5 cm between the stainless-steel/glass reactor [channel dimensions = 1000 pm (width) x 107 pm (depth) x 2.2 m (length)] and the light source, an acetone solution of the nitrite... [Pg.200]

Ogunye and Ray (1971a,b) have formulated the optimal control problem for tubular reactors with catalyst decay via a weak maximum principle for this distributed system. Detailed numerical examples have been calculated for both adiabatic and isothermal reactors. For irreversible reactions, constant conversion policies are found to not always be optimal. A practical technique for on-line optimal control for fixed bed catalytic reactors, has been suggested by Brisk and Barton (1977). Lovland (1977) derived a simple maximum principle for the optimal flow control of plug flow processes. [Pg.468]

Sammells AF, Barton TF, Peterson DR, Harford ST, Mackay R. Methane conversion to syngas in mixed-conducting membrane reactors. Proceedings of the 4th International Conference on Catalysis in Membrane Reactors, Zaragoza, Spain, 3-5 July 2000. [Pg.26]

Sammels AF, Barton TF, Mundschau MV. Catalytic membrane reactors for gas, liquid tmd solid reforming to syngas. 225th American Chemical Society National Meeting - Fuel Division Preprint, New Orleans, LA, 2003. [Pg.80]

A. E. Sammells, T. F. Barton, M. V. Mundschau, Catalytic Membrane Reactors for Gas, Liquid and Solid Reform-... [Pg.212]

The Barton method yields a 70—80% oxidized leady oxide. At high reactor temperatures, the oxide is entirely orthorhombic. At low temperatures, tet-PbO is formed along with ortho-rhomb-PbO. Small amounts of PbO and Pb304 can also be obtained by this method. [Pg.229]

At present the Barton-Mstrlsite transducer unit and the electronic monitoring system (Avien) used in the BSD Beactor could be ap[ ied to the older reactors successfully. However the cost is in excess of 1000 per channel monitored. [Pg.44]

Gibson, S.B., 1976. The design of new chemical plant using hazard analysis. Process Industry Hazards, Symposium Series No. 47. 135 (IChemE. Rugby. UK). HSE, 1992, Tolerability of Risk from Nuclear Power Stations, revised edition. Pantony, M.F.. Scilly. N.F. and Barton. J.A.. 1989. Safety of exothermic reactions a UK strategy, Int Symp on Runaway Reactions. 504—524 (CCPS, AIChE. USA). Kauffman, D. and Chen, H-J.. 1990, Fault-dynamic modelling of a phthalic anhydride reactor, J Loss Prev Process hid. 3 386-394. [Pg.158]

Adams Barton, 2009) also model a WGSR reactor using a heterogeneous modeling approach. The intrinsic rate expression is from Hla et al. previous article. The parameters are result for the best fit estimation. [Pg.56]

Adams II, Thomas A. and Barton, Paul I. (2009). A dynamic two-dimensional heterogeneous model for water gas shift reactors. International Journal of Hydrogen Energy 34, 8877-8891. [Pg.73]

Adams II and Barton [127] used a dynamic heterogeneous model for water-gas shift reactors. The choice for this description was justified by previous reports of large (60°C) temperature differences between the catalyst bed and the gas. They also considered the internal diffusion-reaction problem in large catalyst pellets for industrial-scale applications. The difference between the catalyst core temperature and the one in the gas phase was simulated over the reactor axial position and time. [Pg.70]

Barton, R. A., Sims, H. E. A comparison of the predictions of the Inspect reaction set with experimental data. Proc. 3. CSNI Workshop on Iodine Chemistry in Reactor Safety, Tokai-mura, Japan, 1991 Report JAERI-M 92-012 (1992), p. 346-361... [Pg.658]

J. A. Barton, P. F. Nolan, Safety of chemical batch reactors and storage tanks, ECSC, EEC, EAEC, Brussels, 1991. [Pg.590]

J., Fletcher, D., and Barton, G. (2015) Mixing in bubble column reactors experimental study and CFD modeling. Chem. Eng. /, 264, 291-301. [Pg.127]


See other pages where Barton reactor is mentioned: [Pg.198]    [Pg.236]    [Pg.198]    [Pg.223]    [Pg.198]    [Pg.236]    [Pg.198]    [Pg.223]    [Pg.576]    [Pg.362]    [Pg.306]    [Pg.198]    [Pg.54]    [Pg.73]    [Pg.68]    [Pg.576]    [Pg.229]    [Pg.158]    [Pg.657]    [Pg.277]    [Pg.584]    [Pg.584]    [Pg.206]    [Pg.456]    [Pg.515]   
See also in sourсe #XX -- [ Pg.185 ]




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