Organic compounds -- part of the class 532-570 series – Organic compounds – Oxygen containing
Reexamination Certificate
2002-08-20
2003-12-16
Keys, Rosalynd (Department: 1621)
Organic compounds -- part of the class 532-570 series
Organic compounds
Oxygen containing
C568S623000, C568S624000
Reexamination Certificate
active
06664428
ABSTRACT:
The present invention relates to a process for the preparation of polyetherpolyols.
Polyetherpolyols are provided in large amounts, in particular for the production of polyurethane foams. The known processes for the production of polyetherpolyols are carried out as a rule from alkylene oxides in the presence of a short-chain initiator with the use of different catalysts, such as bases, water-repellent double-layer hydroxides, acidic or Lewis acid systems, organometallic compounds or multimetal cyanide complexes.
Heterogeneous multimetal cyanide complex catalysts are highly selective and active catalysts which are suitable in particular for the production of flexible-foam polyetherpolyols, where high molecular weight has to be achieved and where long oxalkylation times are required. By using multimetal cyanide complex catalysts, the production costs can be reduced and at the same time high-quality polyetherpolyol, which can be further processed to give polyurethane foams which have little odor and are therefore of high quality, can be obtained. The literature discloses that secondary reactions which may lead to the formation of odorous substances and unsaturated components scarcely occur.
However, as a result of the high activity, the heat of reaction can no longer be removed in conventional reactors. If the polyetherpolyol preparation catalyzed by a multimetal cyanide complex is carried out in standard stirred kettles, the metering rates of the alkylene oxide are limited by the heat removal rate of the heat exchangers.
U.S. Pat. No. 5,811,595 proposes an ideally mixed reactor having one or two heat exchangers. The polyetherpolyol is fed into the circulation stream of the heat exchanger, and the ethylene oxide into the reactor. Mixing of the ethylene oxide with the liquid phase is achieved by a nozzle.
Disadvantages of this process are the high circulation rate, which is required for maintaining the high heat removal capacities, and the danger of mechanical damage to the heterogeneous catalyst by the pump. Furthermore, the highly reactive ethylene oxide is introduced into the reactor, in which, owing to the cooling coils used, the heat removal is particularly poor, in particular at low filling levels owing to the small exchange area. Overheating due to the high reaction rate are the result and can lead to damage of the product. This may be exacerbated by the poor mixing in the reservoir. Although coiled pipes are provided in the reservoir for cooling, they are very ineffective at low filling levels, owing to the small exchange area.
EP 850 954 describes a process in which the reaction takes place in the gas space above the liquid. The polyetherpolyol is circulated via a heat exchanger by means of a pump and is fed in through nozzles. This results in a large liquid surface. At the same time, ethylene oxide and polyetherpolyols are metered in via nozzles. The large surface results in good mass transfer and hence high reaction rates.
Owing to the high reaction rate which can be achieved with this process, local excess temperatures in the individual droplets are to be expected, which in turn result in damage to the product. Furthermore, here too the high circulation rate required for heat removal is not without problems for the heterogeneously dispersed multimetal cyanide complex catalyst; the danger of damage cannot be ruled out.
The artificially enlarged gas phase is still a potential danger, in particular in the case of ethoxylation, since free alkylene oxide is present in the gas phase. Ethylene oxide tends to gas-phase decomposition, which may lead to bursting of the reactor. On the other hand, when the polyetherpolyol or ethylene oxide is passed into the liquid, rapid reaction of the alkylene oxide is to be expected owing to the multimetal cyanide complex present.
EP-B-0 633 060 discloses a reactor for gas-liquid reactions, comprising a central stirring apparatus around which heat exchanger plates through which a heat-exchange medium flows are arranged at an angle of from 0 to 70° in the direction of rotation of the stirrer relative to the reactor radius. Higher productivity, a high product quality and reduced catalyst consumption can be ensured by direct removal of heat at its point of generation. The reactor of EP-B-0 633 060 was proposed in particular for highly exothermic catalytic hydrogenation reactions.
It is an object of the present invention to provide a process which employs simple apparatus for the preparation of polyetherpolyols in the presence of multimetal cyanide complex catalysts with improvement of the space-time yield and avoidance of local overheating and hence a higher level of secondary reactions, i.e. with a guarantee of high product quality.
We have found that this object is achieved by a process for the preparation of polyetherpolyols by reacting diols or polyols with ethylene oxide, propylene oxide, butylene oxide or a mixture thereof in the presence of a multimetal cyanide complex catalyst in a stirred kettle reactor.
In the invention, the reaction mixture is circulated via an external heat exchanger by means of a pump.
It is known that KOH-catalyzed, i.e. homogeneously catalyzed polyetherpolyol preparation can be carried out in a stirred kettle reactor having an external heat exchanger. As a result of the removal of heat in the external heat exchanger, there is no limitation of the heat exchanger areas by the reactor dimensions.
With the use of a heterogeneous catalyst, for example a multimetal cyanide complex catalyst, corresponding to the process of the present invention, however, problems are likely to arise with regard to the deposition of catalyst in the heat exchanger and in the circulation pipes and mechanical damage to the catalyst as a result of the circulation.
Surprisingly, however, it was found that there is no deposition of the fine catalyst in the pump circulation or in the heat exchanger.
Moreover, in spite of the very high circulation rates, no mechanical damage to the catalyst as a result of the shear processes between the running boxes of the pump was observed, which damage would have been expected for a suspended heterogeneous catalyst.
There are no restrictions with regard to the stirred kettle reactors which may be used. Vertical, in particular cylindrical reactors having, preferably, a central stirrer are preferably used. The starting materials are fed into the liquid reaction mixture in the stirred kettle. The reaction mixture is circulated via an external heat exchanger by means of a pump.
Various types of pumps may be used for circulating the reaction mixture.
A screw pump is particularly preferably used for this purpose. In this type of pump, the spindles, owing to the particular profile design of the thread flanks, form sealed chambers whose content is displaced axially and completely continuously from the suction side to the pressure side of the pumps on rotation of the spindles. Screw pumps have the advantage that their delivery is substantially independent of the viscosity, which changes in the course of the reaction. Consequently, sufficient heat removal can be ensured at any time during the reaction.
There are in principle no restrictions with regard to the external heat exchanger. Particularly preferably, the heat exchanger is in the form of plates or coils. Coil-type heat exchangers have the advantage that they subject the catalyst to less mechanical stress. This type of heat exchanger is therefore also used for the preparation of dispersions.
The pump delivery is preferably adjusted so that the reactor content is circulated from 5 to 100, preferably from 20 to 50, times per hour. The concentration of the multimetal cyanide complex catalyst in the reaction mixture is preferably adjusted to <250 ppm, preferably <100 ppm, particularly preferably <50 ppm, based on the total amount of product obtained in the reactor. The process is particularly preferably carried out by the semibatch procedure, i.e. initiator and catalyst are initially taken and the alkylene oxides are metered into the reactor. The heat of rea
Bauer Stephan
de Vocht Peter
Grosch Georg Heinrich
Harre Kathrin
Höppner Gerd
BASF - Aktiengesellschaft
Borrego Fernando A.
Keys Rosalynd
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