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Recycling of process streams

Higher degree of integration for process units and recycle of process streams are mainly responsible for a higher degree of interaction between units. Recycling streams may introduce... [Pg.4]

Stenberg, K., Tengborg, C., Galbe, M. et al. (1998). Recycling of process streams in ethanol production from softwoods based on enzymatic hydrolysis. Applied Biochemistry and Biotechnology, 70-72(1), 697-708. [Pg.102]

The catalytic vapor-phase oxidation of propylene is generally carried out in a fixed-bed multitube reactor at near atmospheric pressures and elevated temperatures (ca 350°C) molten salt is used for temperature control. Air is commonly used as the oxygen source and steam is added to suppress the formation of flammable gas mixtures. Operation can be single pass or a recycle stream may be employed. Recent interest has focused on improving process efficiency and minimizing process wastes by defining process improvements that use recycle of process gas streams and/or use of new reaction diluents (20-24). [Pg.123]

The manufacture of food chemicals, whether it involves chemical or biological synthesis and purification, or recovery from natural materials, has a number of characteristics that must be taken into account in establishing a system of good manufacturing practice. For example, in the production of many chemicals, recycling of process liquors and recovery from waste streams are necessary for reasons of quality, economics, and environmental protection. In addition, the production of some food chemicals involves processes in which chemical and biochemical mechanisms have not been fully elucidated, and thus the methods and procedures for materials accountability usually will differ from those applicable to the manufacture of other classes of materials. [Pg.1026]

Strides have been made in industrial-scale production of MAO. Process improvements afford greatly improved yields. This has been achieved by use of alternative reactants and/or continuous processes, employing highly dilute solutions, low ratios of water to TMAL and recycle of intermediate streams (17). [Pg.77]

Having considered the separation and recycling of material, the streams entering and leaving the process can now be established. Figure 4.17 illustrates typical input and output streams. Feed... [Pg.121]

Liquid Effluents. Recycling of acid, soda, and zinc have long been necessary economically, and the acid—soda reaction product, sodium sulfate, is extracted and sold into other sectors of the chemical industry. Acid recovery usually involves the degassing, filtering, and evaporative concentration of the spent acid leaving the spinning machines. Excess sodium sulfate is removed by crystallization and then dehydrated before sale. Traces of zinc that escape recovery are removable from the main Hquid effluent stream to the extent that practically all the zinc can now be retained in the process. [Pg.353]

Iodine Pentafluoride. Iodine pentafluoride is produced by the reaction of iodine and fluorine. Because iodine has a high melting poiat, the reaction is either performed ia a solvent or the reaction is maintained at a temperature where the iodine is Hquid. In a continuous process usiug a solvent (104), ca 1% I2 is dissolved iu IF and passed to a reactor where it is contacted with F2 gas. The IF is continuously discharged from the reactor where a small portion is taken off as product and the larger portion of the stream is recycled. [Pg.186]

The typical SEA process uses a manganese catalyst with a potassium promoter (for solubilization) in a batch reactor. A manganese catalyst increases the relative rate of attack on carbonyl intermediates. Low conversions are followed by recovery and recycle of complex intermediate streams. Acid recovery and purification involve extraction with caustic and heat treatment to further decrease small amounts of impurities (particularly carbonyls). The fatty acids are recovered by freeing with sulfuric acid and, hence, sodium sulfate is a by-product. [Pg.344]

In 1980, >1 one million ts of sodium sulfate were consumed in the United States, but this had declined to <600, 000 t by the end of 1994. The decline is partly a result of higher energy prices and more efficient use of Na2S04 by the paper industry. At one time the kraft paper industry consumed two-thirds of sodium sulfate production. Pressures on paper producers to clean effluent streams and reduce energy forced improvements in internal processes and recycling of sodium sulfate (11,12). [Pg.206]

First Carbonation. The process stream OH is raised to 3.0 with carbon dioxide. Juice is recycled either internally or in a separate vessel to provide seed for calcium carbonate growth. Retention time is 15—20 min at 80—85°C. OH of the juice purification process streams is more descriptive than pH for two reasons first, all of the important solution chemistry depends on reactions of the hydroxyl ion rather than of the hydrogen ion and second, the nature of the C0 2 U20-Ca " equiUbria results in a OH which is independent of the temperature of the solution. AH of the temperature effects on the dissociation constant of water are reflected by the pH. [Pg.26]

A derivative of the Claus process is the Recycle Selectox process, developed by Parsons and Unocal and Hcensed through UOP. Once-Thm Selectox is suitable for very lean acid gas streams (1—5 mol % hydrogen sulfide), which cannot be effectively processed in a Claus unit. As shown in Figure 9, the process is similar to a standard Claus plant, except that the thermal combustor and waste heat boiler have been replaced with a catalytic reactor. The Selectox catalyst promotes the selective oxidation of hydrogen sulfide to sulfur dioxide, ie, hydrocarbons in the feed are not oxidized. These plants typically employ two Claus catalytic stages downstream of the Selectox reactor, to achieve an overall sulfur recovery of 90—95%. [Pg.215]

The carbon monoxide concentration of gas streams is a function of many parameters. In general, increased carbon monoxide concentration is found with an increase in the carbon-to-hydrogen ratio in the feed hydrocarbon a decrease in the steam-to-feed-carbon ratio increase in the synthesis gas exit temperature and avoidance of reequiUbration of the gas stream at a temperature lower than the synthesis temperature. Specific improvement in carbon monoxide production by steam reformers is made by recycling by-product carbon dioxide to the process feed inlet of the reformer (83,84). This increases the relative carbon-to-hydrogen ratio of the feed and raises the equiUbrium carbon monoxide concentration of the effluent. [Pg.54]


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