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Refining section

Refining (Section 2 16) Conversion of crude oil to useful ma terials especially gasoline... [Pg.1292]

The reactor off-gas is cooled by one or more heat exchangers and sent to the collection and refining section of the plant. Unreacted benzene and by-products are incinerated. [Pg.457]

Fig. 1. General refinery operations (a) light petroleum refining section (b) heavy feedstock refining section. Fig. 1. General refinery operations (a) light petroleum refining section (b) heavy feedstock refining section.
A horizontal column is typified by the Brodie Purifier, which is shown schematically in Figure 26. Feed enters the column between recovery and refining sections, and crystals exit the refining section and pass through a purifying section. The purifying section is a wash column in which the crystals are contacted with melt generated at the bottom of the column. [Pg.359]

The ethylene oxide recovered in the desorber contains some carbon dioxide, nitrogen, aldehydes, and traces of ethylene and ethane. In the stripper the light gases are separated overhead and vented, and the partially purified ethylene oxide is sent from the bottom of the stripper to the mid-section of a final refining column. The ethylene oxide from the refining section should have a purity of >99.5 mol %. The final product is usually stored as a Hquid under an inert atmosphere. [Pg.457]

Because we need to know how long the refined section of the bar is, it is important to describe the ramping up of the compositions in a quantitative way. We can do this by writing a differential equation which describes what happens as the zone moves from some general position x to a new position x + 8x (Fig. 4.4g). For a bar of unit cross-section we can write the mass conservation equation... [Pg.40]

Purification of a chemical species by solidification from a liquid mixture can be termed either solution crystallization or crystallization from the melt. The distinction between these two operations is somewhat subtle. The term melt crystallization has been defined as the separation of components of a binary mixture without addition of solvent, but this definition is somewhat restrictive. In solution crystallization a diluent solvent is added to the mixture the solution is then directly or indirectly cooled, and/or solvent is evaporated to effect crystallization. The solid phase is formed and maintained somewhat below its pure-component freezing-point temperature. In melt crystallization no diluent solvent is added to the reaction mixture, and the solid phase is formed by cooling of the melt. Product is frequently maintained near or above its pure-component freezing point in the refining section of the apparatus. [Pg.3]

Section 4.1 provides an overview of the design of object collaborations. Section 4.2 begins with examples of object interactions to show that many variations in interaction protocols achieve the same net effect and so motivate the need for abstract actions. Section 4.3 introduces use cases and relates them to actions and refinement. Section 4.4 explains how actions and effects are related to abstract actions. Section 4.5 describes concurrency between actions and explains how to specify these constraints. [Pg.179]

This book deals with control strategies for integrated plants. In most cases the plant consists of a separate reaction section followed by a refining section with recycles between the two. Optimal designs usually call for tight integration of the unit operations, as we mentioned in Chaps. 2 and 5. What if we could take the ultimate step in integration and combine the reaction and separation sections "We would then have reactive distillation. [Pg.193]

If we use distillate flow from the recycle column to control overhead receiver level, then we see that all of the flows around the liquid recycle loop are set on the basis of level. This violates our original statement to fix the toluene recycle flow. We are then left with the question how to control the overhead receiver level in the recycle column. We can use the fresh makeup toluene feed to control this level since it represents the toluene inventory in the process. Such a scheme limits large flowrate changes to the refining section and automatically ensures the component balance for toluene. [Pg.302]

The synthetic crude is passed to a refining section where the various hydrocarbons are separated and processed to produce transport fuels. [Pg.211]

Opening of equipment for maintenance can result in loss of product. Where possible, the liquid should be blown into the previous or next process vessel or drained back into a bucket for recovery. Any product that is recovered that is not badly contaminated can be returned to a separate storage tank upstream in the process. If a substandard or off-spec glycerine tank is provided in the refining section, it can be equipped with an easily removable cover. [Pg.3198]

The Oil and Gas Journal carries a process section in its Annual Refinery Number under the Annual Refining Section-Processing Details. Most of the processes in current use can be found in these special sections. The Oil and Gas Journal has recently been carrying a special type of article called Petrochem Report which usually gives a timely discussion of specific commercial plants. In the Petroleum Engineer, articles on hydrocarbons from petroleum and natural gas are found under Section C, Refining and Gas Processing. This journal publishes a Reference Annual which usually contains more technical articles on hydrocarbon production than do other issues. [Pg.364]

The original X-ray analysis of Hb was at a resolution of 2.8 A. In order to define the X-ray crystal structure better, SR was used to collect the data to 1.7 A at LURE (Fermi, Perutz, Shaanan and Fourme 1984) and then to 1.5 A at the SRS Daresbury (Waller and Liddington (1990) see section 10.1 case study C). The extra precision of the X-ray analyses and model refinements (section 2.6) of Hb (Liddington 1985) confirmed the original interpretation of Perutz (1970) and brought the Fe-Npyrroie distance in excellent agreement with the EXAFS value (Perutz et al 1982). [Pg.70]

The energy balnace for the refining section is then determined by... [Pg.634]

Using these assumptions, the jacketed cooling areas requited for the recoveiy and refining sections are... [Pg.635]

QrrI heat outflow from refining section... [Pg.639]

Crude alcohol passes to the refining section (3) where low levels of residual methyl esters are converted to wax esters and recycled to the hydrogenation section (2). A refining column removes light and heavy impurities, and the refined fatty alcohol product is polished to convert any residual carbonyls to alcohols. [Pg.183]


See other pages where Refining section is mentioned: [Pg.458]    [Pg.1993]    [Pg.7]    [Pg.223]    [Pg.132]    [Pg.253]    [Pg.726]    [Pg.458]    [Pg.156]    [Pg.1346]    [Pg.1751]    [Pg.2442]    [Pg.3194]    [Pg.2162]    [Pg.377]    [Pg.253]    [Pg.627]    [Pg.630]    [Pg.634]    [Pg.634]    [Pg.634]    [Pg.2146]    [Pg.256]    [Pg.1997]   
See also in sourсe #XX -- [ Pg.72 ]

See also in sourсe #XX -- [ Pg.92 ]




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