Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...
Reexamination Certificate
2001-01-17
2003-01-07
Solola, T. A. (Department: 1626)
Organic compounds -- part of the class 532-570 series
Organic compounds
Heterocyclic carbon compounds containing a hetero ring...
C585S301000, C585S435000
Reexamination Certificate
active
06504038
ABSTRACT:
The present invention relates to a process for the joint preparation of styrene and propylene oxide.
Such process is known in the art and is commonly referred to as styrene monomer/propylene oxide (SM/PO) process. In general, a SM/PO process comprises the steps of:
(a) reacting ethene and benzene to form ethylbenzene,
(b) reacting ethylbenzene with oxygen or air to form ethylbenzene hydroperoxide,
(c) reacting at least part of the ethylbenzene hydroperoxide obtained with propene in the presence of an epoxidation catalyst to form propylene oxide and 1-phenyl ethanol, and
(d) dehydrating at least part of the 1-phenyl ethanol obtained into styrene in the presence of a suitable dehydration catalyst.
The above SM/PO process is well known in the art. In step (a) ethylbenzene is formed by the alkylation of benzene in an ethylbenzene unit. The benzene can, for instance, be derived from a platformer, whilst ethene can be derived from a steam cracking unit. The alkylation reaction may be carried out in various ways known in the art. This reaction can for instance be carried out as a gas phase or liquid phase reaction using an aluminium chloride catalyst-based catalyst. Solid phosphoric acid catalysts or solid acid catalysts based on alumina activated with boron trifluoride are also used in certain benzene alkylation processes for producing ethylbenzene. A further suitable process is the process known as the Mobil/Badger process. In this process a synthetic zeolite catalyst, ZSM-5, is used. In this process the reaction is typically carried out at high temperatures (usually 380-420° C.) and moderate pressure. The preparation of ethylbenzene from ethene and benzene over a zeolitic catalyst is disclosed in U.S. Pat. No. 4,107,224.
Step (a) of the process can be carried out independently from process steps (b) to (d), i.e. at a different location. However, it is preferred that the ethylbenzene production matches the styrene production in step (d), so that the ethylbenzene unit is an integrated part of the SM/PO process or is located in the vicinity of a SM/PO plant. A SM/PO plant with an integrated ethylbenzene unit is generally preferred.
In the oxidation step (b) liquid phase oxidation of ethylbenzene into ethylbenzene hydroperoxide occurs at a temperature of 100-160° C., suitably 130-150° C., and at a pressure of 1-4 bar, suitably 2-3 bar. The oxidation is typically carried out with air as the oxidizing gas, but oxygen may also be applied. The main by-product formed at this stage is acetophenone, which may be hydrogenated in the SM/PO process into 1-phenylethanol, used in step (d) to produce styrene.
In the epoxidation step (c) ethylbenzene hydroperoxide is reacted with propene to yield propylene oxide and 1-phenyl ethanol or substituted 1-phenyl ethanol. In such epoxidation step a homogeneous catalyst or a heterogeneous catalyst can be applied. As homogeneous catalysts molybdenum compounds are frequently applied, while catalysts based on titanium on a silica carrier are often used as heterogeneous catalysts. Conditions under which epoxidation is carried out are known in the art and typically include temperatures of 75 to 150° C. and pressures up to 80 bar with the reaction medium being in the liquid phase. The effluent from the epoxidation step is normally first subjected to a separation treatment to remove the propylene oxide formed, after which the residual stream, containing 1-phenyl ethanol, is suitably subjected to one or more further separation treatments, inter alia to remove ethyl benzene for reuse in an earlier stage of the process. The eventually obtained 1-phenyl ethanol containing stream is then subjected to the dehydration treatment in step (d)
The dehydration of 1-phenyl ethanol into styrene is also well known in the art. It can be carried out both in the gas phase and in the liquid phase. Suitable dehydration catalysts include for instance acidic materials like alumina, alkali alumina, aluminium silicates and H-type synthetic zeolites. Dehydration conditions are also well known and usually include reaction temperatures of 100-210° C. for liquid phase dehydration and 210-320° C., typically 280-310° C., for gas phase dehydration. Pressures usually range from 0.1 to 10 bar. In principle any known dehydration process can be applied in step (d).
In a commercial SM/PO process the propene used in step (c) can be supplied either from an external source or can be made at the SM/PO site itself, normally in a steam cracking unit (also commonly referred to as ethene plant). The latter option is the preferred option and is most frequently applied.
A SM/PO process comprising the steps (a) to (d) as described above requires equal amounts of ethene and propene as feedstock. Because of this, SM/PO plants are typically located in the vicinity of an ethene plant, which produces both the required ethene and propene. Accordingly, if a new SM/PO plant is to be designed and built, this plant is normally either located near an existing ethene plant having an overcapacity of ethene and propene or an ethene plant must be included in the design to ensure the necessary ethene and propene supply. This is not a very advantageous situation from both a logistic and an economic perspective, as it limits the choice of a location for building a SM/PO plant and links the economics to those of an ethene plant. It would, accordingly, be beneficial if ethene and propene could be supplied from an alternative source without having the drawbacks mentioned.
Within the context of the present invention it has been found that integrating a SM/PO process with a fluid catalytic cracking (FCC) unit could overcome the aforesaid economic and logistic constraints.
Accordingly, the present invention relates to a process for the joint preparation of styrene and propylene oxide comprising steps (a), (b), (c) and (d) as described above, wherein the ethene used in step (a) and the propene used in step (c) are at least partly provided by a FCC unit.
A typical FCC unit within the context of the present invention comprises a reactor section and a work-up section. In the reactor section the actual cracking takes place, whereafter in the work-up section the cracked effluent is separated into different products. The reactor section typically comprises a reactor, a catalyst regenerator and a stripper. The temperature in the FCC reactor of the fluid catalytic cracking unit is typically less than about 550° C. and preferably is within the range of from about 500 to about 525° C.
The effluent from the reactor section is then led into the work-up section. Suitably, such work-up section starts with a main fractionator wherein the cracked effluent from the reactor section is introduced. The top fraction of this main fractionator contains the low boiling components, which are mainly C1 to C4 hydrocarbons. Furthermore, gases like hydrogen sulphide, carbonyl sulphide, hydrogen and nitrogen are present in small amounts. This top fraction is typically compressed and routed into an absorption/rectification column. Here the so called off-gas-comprising mainly C1 and C2 components and some hydrogen, nitrogen and sulphur components—is removed and routed, via an unit to remove the sulphur components (typically an amine unit), to the fuel gas system. The C3/C4 material recovered is suitably routed to a debutanizer, a depropanizer and optionally a propane/propene-splitter, where separation into a C4 stream, a propane stream and a propene stream is effected. All treatments starting with the separation in the main fractionator form part of the work-up section.
As indicated above, the off-gas containing the C1 and C2 components from a FCC unit would normally be routed to the fuel gas system. Within the framework of the present invention, however, this off-gas is used as the source of ethene to be used in the ethylbenzene unit. Similarly, the propene used in epoxidation step (c) is derived from the propene/propane-splitter. However, a FCC unit does not produce ethene and propene in the desired ratio of 1:1. It is possible within the framework of the presen
Shell Oil Company
Solola T. A.
Tsang Y. Grace
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