Method for producing an ethylene copolymer

Details Method for producing an ethylene copolymer Method for producing an ethylene copolymer

2001-07-19

2003-07-01

Lipman, Bernard (Department: 1713)

Synthetic resins or natural rubbers -- part of the class 520 ser

Synthetic resins

Polymers from only ethylenic monomers or processes of...

C526S059000, C526S060000, C526S090000, C526S160000, C526S124200, C526S348200, C526S348500, C526S348600

Reexamination Certificate

active

06586540

ABSTRACT:

This application is a U.S. National Stage of International Application PCT/EP00/02234, filed on Mar. 14, 2000 and published on Sep. 28, 2000 in the German language.
The invention relates to a method for producing a copolymer based on ethylene.
Polyethylenes are produced by polymerization of ethylene by two basically different methods, the high-pressure process and the low-pressure/medium-pressure process. The low-pressure/medium-pressure process can be carried out as a solution polymerization, as a suspension/emulsion polymerization or as a gasphase polymerization. The high-pressure process is carried out at pressures higher than 1500 bar and proceeds by a free-radical mechanism.
In general, the low-pressure/medium-pressure process is carried out at pressures below 100 bar and is in general catalyzed. In contrast to the products from the high-pressure process, which have a high degree of branching, lower crystallinity and low density, products from the low-pressure/medium-pressure process usually have a linear, less highly branched structure, have high crystallinity (usually 60-90%), a high melting range (typically 120-135° C.) and high density (usually 0.93-0.97 g/cm
3
). A high density of the polyethylenes is generally associated at the same time with a high glass transition temperature, high hardness, a high melting range, high brittleness and low tack. The above properties generally distinguish the low-pressure/medium-pressure polyethylene.
Since these properties are frequently not technically desired, it is being attempted to reduce the crystallinity of corresponding polyethylenes. This is carried out, for example, by metering small amounts—in general less than 5 mol %—of olefins (comonomers apart from ethylene) into the monomer ethylene, which is subsequently copolymerized with the metered-in olefins. The resultant olefin structural units in the polymer chain increase the disorder in the structure and thus cause lower crystallinity of the polymer. The resultant copolymer, which essentially consists of ethylene structural units, thereby becomes less brittle and can thus be produced more easily for many purposes.
The low-pressure/medium-pressure polymerization of ethylene in which olefins are employed as comonomer will be considered below. This is a copolymerization in which, through variation of the amount of olefin in the monomer mixture, the crystallinity of the resultant product can be controlled. EP-B-0 555 747 describes such a copolymerization of ethylene with comonomer. In the corresponding method, ethylene is polymerized catalytically with &agr;-olefins at pressures below 100 bar.
However, a basic problem occurs in these copolymerizations since, as described in the introduction, the admixture of olefins to the monomer mixture to be polymerized reduces the crystallinity of the resultant polymer product and thus increases its tack and solubility. A frequent consequence is that, in particular in the case of copolymerizations in which a high proportion of comonomer is employed, the reactor used becomes clogged with polymer. Coatings of ethylene copolymer form. These may deposit both in the polymerization reactor and in the discharge zone of the reactor. In particular in narrowed regions of the reactor or in the discharge system of the reactor, blockages can thus easily occur. In practice, corresponding plants, which are generally operated continuously, have to be cleaned regularly. This means that the entire production has to be stopped in order to remove the coatings. The interruption of production means lower occupancy times of the reactor used, thus a fall in production and thus financial consequences.
The present invention has the object of providing a method in which the polyethylene production plant no longer has to be shut down in order to remove coatings. The aim is to remove the interfering coatings during production.
The method according to the invention is then a method for the production of copolymer based on ethylene by continuously operated copolymerization of ethylene and comonomer in a reactor in the presence of a catalyst, where, in a first step of the copolymerization, a mixture comprising ethylene and comonomer of such a composition that a copolymer-containing coating deposits in the reactor is metered into the reactor and/or generated in the reactor, and, in a second step, the concentration of the comonomer in the metered-in mixture and/or in the mixture generated in the reactor is reduced sufficiently and/or the concentration of the ethylene in the metered-in mixture and/or in the mixture generated in the reactor is increased sufficiently that the coating is removed from the reactor either partially or completely.
For the purposes of present invention, the term reactor is taken to mean, inter alia, the entire section of the production apparatus in which the copolymer is able to deposit. This may also be, in particular, the discharge zone of a reactor in which, although the actual polymerization does not take place, polymer is deposited—in particular pipelines are affected by this (the reactor usually contains a production zone and a discharge zone). The comonomer employed in the copolymerization can be one or more species simultaneously. Particularly suitable comonomers are &agr;-olefins, such as butene and/or hexene and/or octene. In principle, however, all alkenes (apart from ethylene) can be employed—including cycloolefins and higher alkenes. If no comonomer is present in the reactor during the second step, owing to the omission of metering-in of comonomer, pure polyethylene can also be generated. In a preferred embodiment, the performance of the second step is only begun when the free internal cross-sectional area of the reactor has first been reduced by at least 5% at any desired point owing to the deposition of polyethylene copolymer-containing coating. In this case, the space-time yield of the method is already significantly reduced and/or there are signs of blockages. In order to prevent damage of this type, the second step is then initiated specifically.
The polymer produced in the first step is softer, has a lower density and is tackier than the product from the second step, which already has a high degree of crystallization. The copolymer produced in step 1 generally has ball indentation hardnesses of from 30 to 50 MPa, preferably from 32 to 42 MPa. The basic standardized determination method for the ball indentation hardness is: (H 132/90): ISO/IEC 2039/1. In step 2, copolymer which has ball indentation hardnesses of greater than 50 NPa is frequently generated.
In general, the duration of step 1 and/or step 2 varies. The smaller the diameter of the discharge lines or the product valves, the more frequently phase 2 has to be initiated. In the case of production units, one step can last from a number of days to a number of weeks. In principle, however, considerably longer and/or shorter times are also possible in this respect. In general, step 2 immediately follows step 1. If the two steps are carried out alternately, step 2 usually immediately follows step 1 and/or step 1 immediately follows step 2. Intermediate steps, for example flushing with inert gas or rinsing with pure dispersion medium, are, however, in principle also possible. At least one further step is then carried out between step 1 and step 2 and/or between step 2 and step 1.
The copolymer-containing coating formed in the copolymerization usually comprises at least 95% by weight of copolymer. Catalyst, for example, may be present in the coating as an impurity.
The suitable catalysts are preferably catalysts for the production of polyolefins, in particular Ziegler, Phillipps or metallocene catalysts. Phillips catalysts are generally employed in supported form. Phillips catalysts are generally chromium catalysts, which, besides chromium, may also contain other elements, such as, for example, molybdenum, tungsten, magnesium or zinc. Particularly suitable support materials for Phillips catalysts are inorganic compounds, in particular porous oxides, such as SiO
2
, Al
2
SiO
3
,

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