Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C67/00—Preparation of carboxylic acid esters
  • C07C67/04—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides onto unsaturated carbon-to-carbon bonds

Definitions

• the present invention relates to a process for the synthesis of esters by reacting an olefin with a lower carboxylic acid in the presence of an acidic catalyst.
• the reaction is carried out in the gaseous phase in the presence of a catalyst consisting of at least one heteropolyacid salt of a metal eg Li, Cu, Mg or K, being supported on a carrier.
• a catalyst consisting of at least one heteropolyacid salt of a metal eg Li, Cu, Mg or K, being supported on a carrier.
• the heteropolyacid used is phosphotungstic acid and the carrier described is silica.
• Impurities such as iron, chromium, molybdenum or nickel usually arise from the corrosion of equipment whereas those of sodium, potassium or calcium result from any water or acetic acid reactant used in the reaction. In particular, these have a tendency to build up in recycle streams, especially in the acid recycle because they are carried over in the vaporiser.
• guard bed or, preferably, a vaporiser.
• the guard bed suitably contains an ion-exchange resin through which the liquid streams pass so as to entrap the metallic or metal compound impurity present.
• Other materials which can be used as a guard bed include amorphous aluminosilicates, clays, zeolites, aluminophosphates, silicoaluminophosphates, metalaluminophosphates and supported heteropolyacids.
• a vaporiser may be designed to minimise carry over of these metallic impurities by using demister pads and/or using a heavy ends take-off at the base of the vaporiser where most of the metal salts will be removed.
• the design of the vaporiser can be such that fresh acid, which is low in heavy metals, can be fed in at the top of the reactor to scrub out metals. This would improve the efficiency of metal removal.
• both a guard bed and a vaporiser are employed to remove metal impurities from the feedstock. The feedstock is first passed through a guard bed as described above, and the liquid exiting the bed (ie the eluate) is introduced into a middle and/or upper region of the vaporiser.
• the olefin reactant used is suitably ethylene, propylene or mixtures thereof. Where a mixture of olefins is used, the resultant product will inevitably be a mixture of esters.
• the source of the olefin reactant used may be a refinery product or a chemical grade olefin which invariably contains some alkanes admixed therewith.
• the other feedstock such as acid, water and recycle streams, in particular, may contain metal or metal compound impurities which have to be removed as described above prior to being brought into contact with the acid catalyst.
• the saturated, lower aliphatic mono-carboxylic acid reactant is suitably a Cl-
• the mole ratio of olefin to the lower monocarboxylic acid in the reactant gases fed to the first reactor is suitably in the range from 1:1 to 18 : 1, preferably from 10: 1 to 14: 1.
• the reactant gases come into contact with the heteropolyacid in a catalyst bed, at least some of the acid is used up to form the ester in an exothermic reaction and the mole ratio of olefin to monocarboxylic acid increases considerably from a starting ratio of 12:1 to about 30:1 in the exit gases from the final reactor.
• the exit gases from the first reactor are fed as the feed gas to the second reactor and the exit gases from the second reactor are fed as the feed gas to the third reactor and so on.
• the olefin to monocarboxylic acid mole ratio in the feed gas to the second and subsequent reactors is seriously depleted due to the acid being used up in the formation of the ester.
• This mole ratio of olefin to monocarboxylic acid is brought to the desired range by injecting further aliquots of the monocarboxylic acid to the feed gas prior to its entry into each of the second and subsequent reactors.
• this range of mole ratios of ethylene to acetic acid in the reactant gases fed to the first reactor is suitably in the range from 1:1 to 18: 1, preferably from 10:1 to 14:1 and that of the feed gas to the second and subsequent reactors is suitably from 10:1 to 16:1.
• the addition of further aliquots of the monocarboxylic acid to the feed gas to the second and subsequent reactors should be sufficient to bring the mole ratio of the olefin to acid within this range of 10 : 1 to 16 : 1.
• the plurality of reactors set up in series referred to above need not be a descrete set of individual reactors.
• the process of the present invention may work equally as effectively if the reaction is carried out in one long reactor which has a plurality of catalyst beds set up in series and the acid is injected into the exit gases from the first bed to maintain the range of olefin to monocarboxylic acid within the predetermined range in the second and subsequent stages.
• the reactors used in this context are suitably run under adiabatic conditions. Due to the exothermic nature of the reaction, it may be necessary to cool the feed gases to the second and subsequent reactors so as to maintain the reaction temperature within the desired range. This cooling may be achieved either by inserting an intermediate cooling step between the each of the reactors and can be wholly or partially replaced by the injection of the acid into the feed gas to the second and subsequent reactors.
• the intermediate cooling step can also be used where a single long reactor which has a plurality of catalyst beds set up in series is used. In this latter case, the intermediate cooling step is used to cool the reactant gases entering the second and subsequent catalyst beds. Where a cooling step is used, this may be achieved eg by using one or more of heat exchanger tubes and by injection of the additional monocarboxylic acid reactant into the feed gases as described above.
• the process of the present invention can be improved further by the addition of water as a component of the reaction mixture.
• the water added to the reaction mixture is suitably present in the form of steam and is capable of generating a mixture of esters and alcohols in the process. It has been found that the presence of water in the reaction mixture in an amount of 1-10 mole %, preferably from 3 to 7 mole %, eg 5 to 6.5 mole % (based on the total moles of acetic acid, olefin and water) enhances the stability of the catalyst and thereby enhances the efficiency of the process.
• water addition may also be used to supplement the cooling of the feed gases to the second and subsequent reactors. It has further been found that dosing the reaction mixture with amounts of a di-ether such as eg diethyl ether, as a co-feed also reduces the formation of undesirable by-products.
• a di-ether such as eg diethyl ether
• the amount of di-ether co-fed is suitably in the range from 0.1 to 6 mole %, preferably in the range from 0.1 to 3 mole % based on the total reaction mixture comprising the olefin, the aliphatic carboxylic acid, water and diethyl ether.
• the di-ether co-fed may correspond to the by product di-ether from the reaction generated from the reactant olefin. Where a mixture of olefins is used, eg a mixture of ethylene and propylene, the di-ether may in turn be an unsymmetrical di-ether.
• the di-ether co-feed may thus be the by-product of the reaction which byproduct is recycled to the reaction mixture.
• heteropolyacid as used herein and throughout the specification in the context of the catalyst is meant to include the free acids.
• the heteropolyacids used to prepare the esterification catalysts of the present invention therefore include inter alia the free acids and co-ordination type partial acid salts thereof in which the anion is a complex, high molecular weight entity.
• the anion comprises 2-18 oxygen- linked polyvalent metal atoms, which are called peripheral atoms. These peripheral atoms surround one or more central atoms in a symmetrical manner.
• the peripheral atoms are usually one or more of molybdenum, tungsten, vanadium, niobium, tantalum and other metals.
• the central atoms are usually silicon or phosphorus but can comprise any one of a large variety of atoms from Groups I- VIII in the Periodic Table of elements. These include, for instance, cupric ions; divalent beryllium, zinc, cobalt or nickel ions; trivalent boron, aluminium, gallium, iron, cerium, arsenic, antimony, phosphorus, bismuth, o chromium or rhodium ions; tetravalent silicon, germanium, tin, titanium, zirconium, vanadium, sulphur, tellurium, manganese nickel, platinum, thorium, hafnium, cerium ions and other rare earth ions; pentavalent phosphorus, arsenic, vanadium, antimony ions; hexavalent tellurium ions; and heptavalent iodine ions.
• cupric ions divalent beryllium, zinc, cobalt or nickel ions
• Heteropolyacids usually have a high molecular weight eg in the range from 700-8500 and include dimeric complexes. They have a relatively high solubility in polar 0 solvents such as water or other oxygenated solvents, especially if they are free acids and in the case of several salts, and their solubility can be controlled by choosing the appropriate counter-ions.
• polar 0 solvents such as water or other oxygenated solvents
• heteropolyacids that may be used as the catalysts in the present invention include:
• the heteropolyacid catalyst whether used as a free acid or as a partial acid salt thereof is suitably supported, preferably on a siliceous support.
• the siliceous support is suitably in the form of granules, beads, agglomerates, globules, extrudates or pellets.
• the siliceous support used can be derived from an amorphous, non-porous synthetic silica especially fumed silica, such as those produced by flame hydrolysis of SiCl 4 .
• Specific examples of such siliceous supports include Support 350 made by pelletisation of AEROSLL® 200 (both ex Degussa).
• the support suitably has a crush strength of at least 2 Kg force, suitably at least 5 Kg force, preferably at least 6 Kg and more preferably at least 7 Kg.
• the crush strengths quoted are based on average of that determined for each set of 50 beads/globules on a CHATTLLLON tester which measures the minimum force necessary to crush a particle between parallel plates.
• the bulk density of the support is suitably at least 380 g/1, preferably at least 440 g/1.
• the siliceous support is suitably free of extraneous metals or elements which might adversely affect the catalytic activity of the system.
• the siliceous support suitably has at least 99% w/w purity, ie the impurities are less than 1% w/w, preferably less than 0.60% w/w and more preferably less than 0.30% w/w.
• silica supports are the Grace 57 and 1371 grades of silica.
• - Grace 57 grade silica has a bulk density of about 0.4 g/ml and a surface area in the range of 250-350 m 2 /g.
• Grace silica grade No. 1371 has an average bulk density of about 0.39 g/ml, a surface area of about 500-550 m 2 /g, an average pore volume of about 1.15 ml/g and an average particle size ranging from about 0.1-3.5 mm.
• These supports can be used as such or after crushing to an average particle size in the range from 0.5-2 mm and sieving before being used as the support for the heteropolyacid catalyst.
• the impregnated support is suitably prepared by dissolving the heteropolyacid, which is preferably a tungstosihcic acid, in eg distilled water, and then adding the support to the aqueous solution so formed.
• the support is suitably left to soak in the acid solution for a duration of several hours, with periodic manual stirring, after which time it is suitably filtered using a Buchner funnel in order to remove any excess acid.
• the wet catalyst thus formed is then suitably placed in an oven at elevated temperature for several hours to dry, after which time it is allowed to cool to ambient temperature in a desiccator.
• the weight of the catalyst on drying, the weight of the support used and the weight of the acid on support was obtained by deducting the latter from the former from which the catalyst loading in g/litre was determined.
• This supported catalyst (measured by weight) can then be used in the process of the invention.
• the amount of heteropolyacid deposited/impregnated on the support for use in the reaction is suitably in the range from 10 to 60% by weight, preferably from 20 to 50% by weight based on the total weight of the heteropolyacid and the support.
• the products of the reaction are recovered by eg fractional distillation.
• the esters produced may be hydrolysed to the corresponding alcohols or mixture of alcohols in relatively high yields and purity.
• the process of the present invention is particularly suited to making ethyl acetate from ethylene and acetic acid by an addition reaction with optional recycle of any ethanol or diethyl ether formed.
• the present invention is further illustrated with reference to the following
• Silica granules (Grace 57 grade, surface area 310 m 2 /g, bulk density 0.4 g/ml, pore volume 1.03 ml/g, ca. 5-8 mm, 9.3 kg, ex W R Grace) were soaked in a solution of silicotungstic acid [H4SiWi2 ⁇ 40-26H2 ⁇ ] (32 kg of 26% w/w aqueous solution) in order to impregnate the silica support with the silicophosphoric acid catalyst. After this duration, excess catalyst solution was drained off. The resultant catalyst impregnated support granules were then dried using a warm nitrogen stream to give a catalyst with a loading of 140 g/litre. Catalyst Testing:
• Three reactors designed to simulate an adiabatic operation, were set up in series with intercoolers.
• the feedstream was heated in a vaporiser and passed into the top of the first reactor at 176°C and lOOOKpa pressure.
• the exit gases from the top reactor were cooled and fed into the second reactor at 172°C and the exist gases from this second reactor were cooled and fed into a third reactor at 168°C.
• the exit gases from the third reactor were cooled and passed into a vapour-liquid separator at - 30°C.
• the vapour stream from the separator was compressed and recycled to the vaporiser.
• the liquid stream from the separator was reduced in pressure to atmospheric and samples were analysed by gas chromatography.
• the top bed was replaced with fresh catalyst and a further 200hour period monitored.
• the fresh acid/water feed now contained O. ⁇ ppm calcium.
• 4wt% EtOH were passed through a 20 cm3 Purolite® CT145 cation resin bed at a flow rate of 190 mis/hour.
• the liquid entering this resin bed contained transition metals simulating the presence of corrosion metals at concentrations of 40 ppm iron, 10 ppm nickel and 10 ppm chromium. This bed removed these corrosion metals to a concentration of less than

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• 1998
  • 1998-07-14 GB GBGB9815135.0A patent/GB9815135D0/en not_active Ceased
• 1999
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