Reactor polyethylene, high pressure

LDPE, also known as high pressure polyethylene, is produced at pressures ranging from 82—276 MPa (800—2725 atm). Operating at 132—332°C, it may be produced by either a tubular or a stirred autoclave reactor. Reaction is sustained by continuously injecting free-radical initiators, such as peroxides, oxygen, or a combination of both, to the reactor feed. 

An independent development of a high pressure polymerization technology has led to the use of molten polymer as a medium for catalytic ethylene polymerization. Some reactors previously used for free-radical ethylene polymerization at a high pressure (see Olefin polymers, low density polyethylene) have been converted to accommodate catalytic polymerization, both stirred-tank and tubular autoclaves operating at 30—200 MPa (4,500—30,000 psig) and 170—350°C (57,83,84). CdF Chimie uses a three-zone high pressure autoclave at zone temperatures of 215, 250, and 260°C (85). Residence times in all these reactors are short, typically less than one minute. 

The computer model consists of the numerical integration of a set of differential equations which conceptualizes the high-pressure polyethylene reactor. A Runge-Kutta technique is used for integration with the use of an automatically adjusted integration step size. The equations used for the computer model are shown in Appendix A. 

High pressures are required for many commercial chemical processes. For example, the synthesis of ammonia is carried out at reactor pressures of up to 1000 bar, and high-density polyethylene processes operate up to 1500 bar. 

Low density polyethylene is made at high pressures in one of two types of continuous reactor. Autoclave reactors are large stirred pressure vessels, which rely on chilled incoming monomer to remove the heat of polymerization. Tubular reactors consist of long tubes with diameters of approximately 2.5 cm and lengths of up to 600 m. Tubular reactors have a very high surface-to-volume ratio, which permits external cooling to remove the heat of polymerization. 

You have to shake your head in wonder when you think about how the largest selling plastic was developed—by accident. In 1933, the scientists at the ICI labs in England were attempting to make styrene by the high-pressure reaction of benzaldehyde with ethylene. Instead, they ended up with a reactor lined with a solid, white, wax-like material—polyethylene. 

A number of processes have been developed to obtain products of different physical properties. The nature of the product is affected by the addition of diluents or other additives before carrying out the polymerization. Autoclaves or stirred-tank reactors, and tubular reactors, or their combinations have been developed for the industrial production of high-pressure polyethylene.206,440 Pressures up to 3500 atm and temperatures near 300°C are typically applied. 

The first section of this chapter describes the most important high pressure process run under homogeneous conditions to manufacture Low Density PolyEthylene (LDPE). The radical polymerization of ethylene to LDPE is carried out in tubular reactors or in stirred autoclaves. Tubular reactors exhibit higher capacities than stirred autoclaves. The latter are preferred to produce ethylene copolymers having a higher comonomer content. 

Loss prevention of polyethylene plants is outlined in Chapter 7.2. The major hazard that can occur is the runaway of the high-pressure reactor and decomposition of ethylene besides fire and disintegration of high-pressure separators, pipes, and compressors. The critical conditions for runaway and ethylene decomposition during homo- and copolymerization are revealed together with the influence of decomposition sensitizers. Relief devices and venting systems are described. 

The major hazard that can occur in the high-pressure polyethylene process is a runaway of the reactor and decomposition of ethylene as well as fires, explosion, and disintegration of high-pressure parts. Although the last incidents are well understood, the reasons for runaway and ethylene decomposition have been evaluated only recently. Experience over twenty years has shown that decomposition mostly takes place in the reactor and in the high-pressure separator, but decompositions have also been reported from ethylene-feed and product lines. 

In recent years metallocene catalysts have been introduced into low-pressure gas-phase-, solution-, and slurry-processes to manufacture polyethylene and polypropylene. The new technology extends not only the range of conventional materials but generates new speciality polymers. Some companies have also retro-fitted high-pressure reactors to make use of the advantages of metallocene catalysts. 

The advantages known from the production of low-density polyethylene (LDPE) become obvious also when metallocene catalysts are used under high-pressure conditions. The compressed monomer can dissolve the polymer which is formed during polymerization, which means that no additional solvent is required for the polymer. The high-pressure polymerization proceeds with a high rate, which requires a short residence time and small reactor volume. Established technology, with stirred autoclaves as well as tubular reactors, can be applied. 

High pressure low density polyethylene resins are produced in two types of reactors. One is a continuous-flow mechanically stirred autoclave (origi-... 

Fig. 5 Autoclave and tubular high pressure polyethylene reactors...

Figure 1. High pressure polyethylene tubular reactor.

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