Preparation of tertiary alkyl ethers

This invention relates to a process for preparing tertiary alkyl ethers from isoolefins and aliphatic alcohols.

More particularly, the invention relates to the preparation of methyl tert-butyl ether or methyl tert-amyl ether from isobutylene and methanol, or isoamylene and methanol respectively.

In the description given hereinafter, reference will be made for reasons of simplicity tc the preparation of methyl tertbutyl ether, however the process is also completely valid for the preparation of all other tert-alkyl ethers, as the differences between the belling points of the components and products ore of the same order of magnitude.

Methyl tert-butyl ether iMTBE) is prepared, according to the known art, by reacting isobutene, which is generally contained in variable percentages in a hydrocarbon fraction, with methanol in the presence of a suitable catalyst generally consisting of sulphonated styrene-divinylbenzene resins, at a temperature which can vary from ambient temperature to about 100°C.

In practice, isobutene is not available on a plant scale, and reference will therefore be made to the aforesaid case of

the hydrocarbon fraction containing isobutene.

The reaction is an equilibrium reaction, and if the methanol quantity used is close to the stoichiometric, the isobutene conversion is 90% or a little more at those temperatures which give a reasonable reaction rate.

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If higher conversions are required, an excess of methanol must be used, and this mist then be separated from the reaction product and recycled, in which case conversions of slightly more than 95% are attained under reasonable

5 conditions, or alternatively the reaction product must be separated and the residual mixture passed to a second reaction stage, which again under approximately stoichiometric conditions enables conversions of about 99% to be

attained.

10 However, there is the problem that in order to carry out

this operation it is necessary to evaporate the components

twice, and use two reactai‘s and two distillation columns so

increasing the investment and running costs.The .most recent ar

(European Patent Applicaticr. published on March 19, 1980 under No 8860, available on request) suggests a method for overcoming the aforesaid problems, by feeding a mixture containing isobutene and methanol to a

distillation column irilea with catalyst suitable for the preparation of MTBE, in which the catalyst elso acts as distillation packing, thus forming MTBE and separating the

20 MTBE from the components at the same time.

However, the method described in the aforesaid patent application suffers from certain serious drawbacks related

to the fact that the catalyst acts as the distillation column packing, and must therefore satisfy special require25 ments, in particular the requirement of a low pressure drop. For this reason, it is used placed in bags forming a belt, which leave ample space for the passage of the vapour and

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liquid, but which on the other hand are difficult to prepare and to load into the column.

The method described in the aforesaid European application also suffers from the drawback that the continuous phase

5 inside the column is represented by the vapour phase, whereas the dispersed phase is the liquid phase, and this leads to low MTBE yields, as the reaction takes place in practice in the vapour phase.

This also leads to the possibility of the formation of 10 substantial dimer quantities because there is an alcohol

deficiency in the vapour'phase.

It has now been surprisingly found possible to obviate all the aforesaid drawbacks by carrying out both the reaction leading to the formation of the tert-alkyl ether (ΜΓΒΞ) and

15 its separation from the hydrocarbons and compounds which accompany it in a single plate fractionating apparatus in which some of the plates are provided with beds of catalyst in the form of spherules based on sulphonated styrenedivinylbenzene resins, suitable for the preparation of the

20 tert-alkyl ether (OTBE).

The process according to the present invention comprises: feeding the hydrocarbon feed containing the isoolefin to a plate fractionating column in which some of the plates are provided with beds of catalyst consisting of sulphonated

25 styrene-divinylbenzene resins and are separated from each other either by groups of fractionating plates or single fractionating plates; feeding the alcohol by itself in

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- 4 proximity to the top of the column, preferably above the last catalyst bed and some plates (between 4 and 8) below the point at which the reflux is fed; reacting the isoolefin with the alcohol on the plates provided with catalyst beds, which are immersed in the liquid containing the alcohol and through which the vapours bubble; and separating the produced ether from the other components at the fractionating plates and at the plates provided with catalyst beds to obtain as bottom product the substantially pure ether, and as overhead product the feed hydrocarbons and possibly the alcohol in the form of an azeotrope with the feed hydrocarbons.

The process according to the present invention in the case of Ml’BE comprises: feeding the hydrocarbon feed containing isobutene to a plate fractionating column in which some of the plates are provided with beds of catalyst consisting of sulphonated styrene-divinylbenzene resins suitable for forming MTBE and are separated from each other either by groups of fractionating plates or single fractionating plates; feeding the methanol by itself in proximity to the top of the column and preferably above the last catalyst bed and between 4 and 8 plates below the point at which the reflux is fed; reacting the isobutene with the methanol on the plates provided with catalyst beds, which are immersed in the liquid containing methanol and through which the vapour bubbles; and separating the produced MTBE from the other components both at the fractionating plates and st the plates provided with catalyst beds, to obtain as bottom product substantially pure MTBE, and

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as overhead product those hydrocarbons other than the isobutene, plus methanol in the quantity corresponding to the azeotrope.

The process according to the present invention is carried out 5 at a pressure of between 500 and 1000 KPa,

The hydrocarbon feed containing the isoolefin is fed to the plate ci~>1 man according to the invention in a position such that at least two plates comprising catalyst beds are above said feed and at least one plate comprising a catalyst bed

10 is below said feed. The vapours produced by the fractionating column reboiler bubble through the catalyst beds, which are preferably not less than three in number, and the methanol and isobutene react therein in the liquid phase which covers each catalyst bed.

15 The catalyst is in the form of spherules having a diameter of between 0.5 and 1 mm, and the thickness of each catalyst

bed is of the order of 1 metre.

The liquid present on each plate containing the catalyst flows on to the lower distillation plate by way of one or

20 more conventional weirs, and the catalyst always remains immersed in the liquid.

The catalyst is retained on each plate by the fact that it is contained by meshes at least at the bed base and top, which prevent it from escaping,

25 The invention will, be more apparent from the accompanying figure which illustrates a non-limiting embodiment thereof.

The reference numeral 1 indicates the fractionating plates,

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and 2 a fractionating plate comprising thereon a catalyst bed 3, which is retained by the meshes 4 and 5.

The liquid follows the path indicated by the arrows 6, passing through the catalyst bed. The vapour follows the

5 upward path indicated by the arrow 7· A non-limiting embodiment of the process according to the invention is

described hereinafter.

EXAMPLE

A distillation column was constructed using flanged pipe

10 sections of diameter 10 cm and length 100 cm, containing six bubble cap distillation plates (two bubble caps per plate). The column was constructed by alternating 1 m pipe sections full of catalyst with sections comprising six plates, to give

8 total of six sections above the feed and two sections below.

15 The column was fed with 2 kg/h of 0^ containing 50% of isobutene.

A reflux ratio of 1:1 was maintained, and 575 g of methanol were fed together with the reflux. The operating pressure was 800 KPa, and the operating temperature was 60°-150°C.

20 The overhead product consisted of 1035 g of containing

30 g of methanol and 5 g of isobutene.

15^0 g of practically pure ΜΤΒΞ were obtained as bottom product.

- 7 WHAT-rrtVE