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Benzene flow sheet

Figure 4.96 Flow sheet of the micro reactor set-up used for methylation of a 1,3,4-trisubstituted benzene [127. ... Figure 4.96 Flow sheet of the micro reactor set-up used for methylation of a 1,3,4-trisubstituted benzene [127. ...
From the compositions given, calculate the stream flows for the production of absolute alcohol from 100 kmol/h raw alcohol feed, composition 89 per cent ethanol, balance water. Take the benzene losses to total 0.1 kmol/h. Draw a preliminary flow-sheet for the process. [Pg.191]

Fig. 1 shows a flow sheet of the equipment used.The three reactants ethybenzene (EB),benzene(B) and diethylbenzene(DEB) could be feeded by thermal massflow-controiers.A fourth thermal massflow-controler was used to feed nitrogen as an... [Pg.257]

The different operating conditions for the methyl and phenyl reactions make it desirable to employ two separate flow sheets to illustrate the production of methyl and phenyl silicones by the direct process. Fig. 2 shows the flow of materials for the production of methyl silicone via the methanol process, and Fig. 3 depicts the production of phenyl silicone from benzene. [Pg.98]

Fig. 11.14. Process flow sheet of cyclohexane/benzene heat pump using hydrogen permeable membranes Rdit and R/rdehydrogenation and hydrogenation reactors C, compressors T, turbine HE, heat exchangers CHE, counter-current heat exchangers P, liquid pump M, hydrogen membranes. Reproduced from Cacciola et al. [133] with permission. Fig. 11.14. Process flow sheet of cyclohexane/benzene heat pump using hydrogen permeable membranes Rdit and R/rdehydrogenation and hydrogenation reactors C, compressors T, turbine HE, heat exchangers CHE, counter-current heat exchangers P, liquid pump M, hydrogen membranes. Reproduced from Cacciola et al. [133] with permission.
Figure 7.2 Simplified flow sheet of the Asahi process for benzene hydrogenation to cydohexene. Figure 7.2 Simplified flow sheet of the Asahi process for benzene hydrogenation to cydohexene.
Phenol. The manufacture of phenol by the oxidation of benzene is described by Denton (21) and by Simons and McArthur (107). The literature on phenol by the oxidation of cumene is partly covered in the reports of Frank (33), Hawkins (43), and Kharasch (57), mentioned earlier. A brief description and flow sheet of the process is given in Chemical Engineering (16). The patents in this field are mainly held by The Distillers Co., Ltd., Hercules Powder Co., and Allied Chemical and Dye Corp. In this phenol process large amounts of acetone are obtained as a coproduct. It should also be noted that the process may be directed to the production of cumene hydroperoxide and a,a dimethylbenzyl alcohol. Krieble (61) and Kenyon and Boehmer (55) describe the preparation of phenol by the chlorination and sulfonation processes. [Pg.374]

Figure 6.46 Flow sheet of an optimized cascade for the separation of a 50% benzene-cyclohexane mixture, product quality 98% benzene and cyclohexane. (At = 7.5 K per membrane unit). Figure 6.46 Flow sheet of an optimized cascade for the separation of a 50% benzene-cyclohexane mixture, product quality 98% benzene and cyclohexane. (At = 7.5 K per membrane unit).
Fig. 3-1. Qualitative block-type process flow sheet for continuous production of benzene hexachloride. (Note This shows both the chemical and physical operations of the process.)... Fig. 3-1. Qualitative block-type process flow sheet for continuous production of benzene hexachloride. (Note This shows both the chemical and physical operations of the process.)...
Fig. 3-5, Material balance flow sheet for a section of the benzene hexachloride process—shows tabular presentation of stream components. Fig. 3-5, Material balance flow sheet for a section of the benzene hexachloride process—shows tabular presentation of stream components.
Reference Manufacture of Benzene Hexachloride, Chap. 3. (Note that the letter-number references, for example, A-1, of equipment in the sections which follow are based on the equipment flow sheet in Pig. 3-2.)... [Pg.152]

Design a 250,000 Ib/yr Lindane (99 per cent 7 isomer of benzene hexachloride) plant based on process information given in the current literature [e.g., see Chem. Eng. Progr., 52 281 (1956) Chem, Week, 78 54 (1956) Ind. Eng. CAem., 48(10) 41A (1956)], Develop the process flow. sheets, equipment specifications, and plant layout. Examine the economics of producing Lindane including (1) fixed and capital cost estimates by one or more of the methods outlined in Chap. 6, (2) profitability analysis showing return on investment and pay-out time, (3) break-even point analysis of the project, (4) economic estimates for a plant producing 500,000 Ib/yr and 750,000 Ib/yr. [Pg.262]

Make an order-of-magnitude estimate of the total capital investment, as of the year 2001 (MS = 1,110), to produce benzene according to the toluene hydrodealkylation process shown in Figure 5.13. Assume an overall conversion of toluene to benzene of 95% and 330 days of operation per year. Also, assume the makeup gas enters at the desired pressure and a clay adsorption treater must be added to the flow sheet after the stabilizer. The treater removes contaminants that would prevent the benzene product from meeting specifications. In addition, in order for the reactor to handle the high temperature, it must have a brick lining on the inside, so take a material factor of Fm = 15. Otherwise, aU major equipment is constructed of carbon steel. The plant will be constructed outdoors with major additions to existing facilities. [Pg.499]

The process developed by Kureha Chemical to produce diisopropylnaphthalene mixtures operates in a manner similar to that of benzene alkylation it comprises three stages consisting of transalkylation, alkylation and distillation of the reaction product. Naphthalene and recycled tri- and tetra-isopropylnaphthalenes first react in a transalkylation stage the product is then fed together with recycled mono-isopropylnaphthalenes to a second stage where the reaction with propene produces mainly diisopropylnaphthalenes. The reaction mixture is split by vacuum distillation. The reaction is performed at 7 bar and 200 using a silica-alumina catalyst. Figure 9.16 shows the flow sheet for the Kureha process. [Pg.330]

Figure 1.7 Piping and Instrumentation Diagram for Benzene Distillation (adapted from Kauffman, D, Flow Sheets and Diagrams, AIChE Modular Instruction, Series G Design of Equipment, series editor J. Beckman, AIChE, New York, 1986, vol 1, Chapter G.1.5, AIChE copyright 1986 AIChE, all rights reserved)... Figure 1.7 Piping and Instrumentation Diagram for Benzene Distillation (adapted from Kauffman, D, Flow Sheets and Diagrams, AIChE Modular Instruction, Series G Design of Equipment, series editor J. Beckman, AIChE, New York, 1986, vol 1, Chapter G.1.5, AIChE copyright 1986 AIChE, all rights reserved)...
Draw a proeess flow sheet for the produetion of phenol via benzene sulfonation. Assuming all reactions proceed with 95% yield. Include mass balance data on your flow sheet. [Pg.57]

Extractive distillation is frequently employed for the separation of mixture with close boiling point. It features by adding an extractive agent to increase the relative volatility of the mixture concerned so as to make the separation easier with less number of theoretical plates or transfer unit required. Liu et al. [37] employed this process for the separation of benzene (boiling point 80.09 °C) and thiophene (boiling point 84.16 °C) in a packed column with N-methyl-2-pyrrolidone (NMP) as the extractive agent. The flow sheet is shown schematically in Fig. 4.46. [Pg.135]

Since we are not generating a flow sheet, simply click on Next to proceed into the Property Table Generation System. Enter the title Density into the Title area by simply clicking on the box and typing it. Click on Next to continue. Enter all components for this example benzene is the only component A base method... [Pg.21]

In a new case in Hysys, add benzene and toluene components and select the appropriate fluid package. Peng-Robinson EOS is a proper fluid package for hydrocarbons. The process flow sheet is shown in Figure 1.42. [Pg.34]

Fig. 6.1 (a) TEM image and (b) Raman spectrum of graphene prepared by the thermal decomposition of methane (70 seem), (c) FESEM image and (d) Raman spectrum of graphene obtained by benzene (argon passed through benzene with flow rate of 200 seem) at 1000 °C on a nickel sheet (from [8]). [Pg.173]

The sheet of porous stainless steel with Re-carbon deposited film divided membrane reactor onto two equal parts. Cyclohexane vapors were fed to the surface of membrane with Re-carbon film (reaction part of membrane reactor) in argon flow from the thermostated bubler. The second part of reactor was flowed by argon and used for the removal of hydrogen, diffused through a membrane catalyst from the reaction zone. The products of reaction were benzene and hydrogen. [Pg.732]

Figure 13.4 Induced currents in a graphite sheet. Local currents (blue) are centered at the carbon nuclei, and interatomic currents (red) are flowing in the jt systems of the benzene rings. The average size (effective radius) of the ring currents in graphite is 7.8 A, which corresponds to an area of about 30 benzene molecules [31] (c.f. the effective... Figure 13.4 Induced currents in a graphite sheet. Local currents (blue) are centered at the carbon nuclei, and interatomic currents (red) are flowing in the jt systems of the benzene rings. The average size (effective radius) of the ring currents in graphite is 7.8 A, which corresponds to an area of about 30 benzene molecules [31] (c.f. the effective...
Al-Megren et al. (2013) apphed a semibatch membrane system and a continuous membrane reactor (flat-sheet membranes of polypropylene and polyethersuUbne) for the direct hydroxylation of benzene using H2O2 as an oxidant. With the help of water on the stripping side of the membrane unit, the produced phenol was recovered. They explored the effect of the hydrophUic and hydrophobic character of the membrane material on the phenol recovery at different flow rates of the feed and the stripping phases. The obtained results showed that the hydrophUic membrane has a better performance. What is more, the continuous removal of the phenol from the reaction side contributed to a reduction in byproduct (such as benzoquinone) formalion and a halt in biphenyl and tars formalion. The performance of a continuous system was better than the semibatch system, mainly because of the total amount of phenol recovered in the permeate. In particular, more than 25% of the produced phenol was recovered in the continuous membrane reactor whereas this value for the semibatch membrane system was less than 1%. [Pg.647]


See other pages where Benzene flow sheet is mentioned: [Pg.357]    [Pg.23]    [Pg.44]    [Pg.90]    [Pg.366]    [Pg.329]    [Pg.196]    [Pg.196]    [Pg.172]    [Pg.124]    [Pg.196]    [Pg.5966]    [Pg.196]    [Pg.196]    [Pg.5965]    [Pg.123]    [Pg.64]    [Pg.509]    [Pg.364]   
See also in sourсe #XX -- [ Pg.373 ]




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