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Reactor design, synthesis

The synthesis of reaction-separation systems. The recycling of material is an essential feature of most chemical processes. The use of excess reactants, diluents, or heat carriers in the reactor design has a significant effect on the flowsheet recycle structure. Sometimes... [Pg.400]

Hydrothermal Synthesis Systems. Of the unit operations depicted in Figure 1, the pressurized sections from reactor inlet to pressure letdown ate key to hydrothermal process design. In consideration of scale-up of a hydrothermal process for high performance materials, several criteria must be considered. First, the mode of operation, which can be either continuous, semicontinuous, or batch, must be determined. Factors to consider ate the operating conditions, the manufacturing demand, the composition of the product mix (single or multiple products), the amount of waste that can be tolerated, and the materials of constmction requirements. Criteria for the selection of hydrothermal reactor design maybe summarized as... [Pg.501]

The U.S. Department of Energy has funded a research program to develop the Hquid-phase methanol process (LPMEOH) (33). This process utilizes a catalyst such as copper—zinc oxide suspended in a hydrocarbon oil. The Hquid phase is used as a heat-transfer medium and allows the reaction to be conducted at higher conversions than conventional reactor designs. In addition, the use of the LPMEOH process allows the use of a coal-derived, CO-rich synthesis gas. Typical reactor conditions for this process are 3.5—6.3 MPa (35—60 atm) and 473—563 K (see Methanol). [Pg.51]

Remarks The aim here was not the description of the mechanism of the real methanol synthesis, where CO2 may have a significant role. Here we created the simplest mechanistic scheme requiring only that it should represent the known laws of thermodynamics, kinetics in general, and mathematics in exact form without approximations. This was done for the purpose of testing our own skills in kinetic modeling and reactor design on an exact mathematical description of a reaction rate that does not even invoke the rate-limiting step assumption. [Pg.225]

Basically, tliere are two classes of anunonia converters, tubular and multiple bed. The tubular bed reactor is limited in capacity to a maximum of about 500 tons/day. In most reactor designs, the cold inlet synthesis gas flows tlirough an annular space between the converter shell and tlie catalyst cartridge. This maintains the shell at a low temperature, minimizing the possibility of hydrogen embrittlement, which can occur at normal synthesis pressures. The inlet gas is then preheated to syntliesis temperature by the exit gas in an internal heat e.xchaiiger, after which it enters tlie interior of the anunonia converter, which contains tlie promoted iron catalyst. [Pg.261]

Jess, A., Popp, R., Hedden, K. 1999. Fischer-Tropsch-synthesis with nitrogen-rich syngas—Fundamentals and reactor design aspects. Applied Catalysis A General 186 321-42. [Pg.227]

A 1969 paper presented a mathematical crystallization model for the continuous crystallization of zeolite A [174]. The successful implementation of continuous synthesis of zeoHtes must accommodate the relatively slow crystallization rates with the reactor design to allow sufficient residence time at the necessary digestion temperature. A recent patent publication describes continuous zeolite synthesis using microwave heating, which couples the often significant advantages of faster zeolite crystallization under microwave radiation with a continuous synthesis, dewatering and work-up process [175],... [Pg.77]

Reactor design uses information, knowledge, and experience from a variety of areas—thermodynamics, chemical kinetics, fluid mechanics, heat transfer, mass transfer, and economics. Chemical reaction engineering is the synthesis of all these factors with the aim of properly designing a chemical reactor. [Pg.1]

Table V shows the salient features of several Fischer-Tropsch processes. Two of these—the powdered catalyst-oil slurry and the granular catalyst-hot gas recycle—have not been developed to a satisfactory level of operability. They are included to indicate the progress that has been made in process development. Such progress has been quite marked in increase of space-time yield (kilograms of C3+ per cubic meter of reaction space per hour) and concomitant simplification of reactor design. The increase in specific yield (grams of C3+ per cubic meter of inert-free synthesis gas) has been less striking, as only one operable process—the granular catalyst-internally cooled (by oil circulation) process—has exceeded the best specific yield of the Ruhrchemie cobalt catalyst, end-gas recycle process. The importance of a high specific yield when coal is used as raw material for synthesis-gas production is shown by the estimate that 60 to 70% of the total cost of the product is the cost of purified synthesis gas. Table V shows the salient features of several Fischer-Tropsch processes. Two of these—the powdered catalyst-oil slurry and the granular catalyst-hot gas recycle—have not been developed to a satisfactory level of operability. They are included to indicate the progress that has been made in process development. Such progress has been quite marked in increase of space-time yield (kilograms of C3+ per cubic meter of reaction space per hour) and concomitant simplification of reactor design. The increase in specific yield (grams of C3+ per cubic meter of inert-free synthesis gas) has been less striking, as only one operable process—the granular catalyst-internally cooled (by oil circulation) process—has exceeded the best specific yield of the Ruhrchemie cobalt catalyst, end-gas recycle process. The importance of a high specific yield when coal is used as raw material for synthesis-gas production is shown by the estimate that 60 to 70% of the total cost of the product is the cost of purified synthesis gas.
Photonitrosylations show an extremely high tendency for filming, and the difficulties in implementing the caprolactam synthesis on an industrial scale are also linked to reactor designs not taking into account the competitive secondary reactions leading to polymerized material. [Pg.241]


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