CA2671361C - Process for carbonylation of aliphatic alcohols and/or reactive derivatives thereof - Google Patents

Abstract

A product comprising a C1-C3 aliphatic carboxylic acid or corresponding ester is produced by a process comprising reacting a C1-C3 aliphatic alcohol or a reactive derivative thereof with carbon monoxide in the presence of a zeolite catalyst having an 8-member ring channel which is interconnected with a channel defined by a ring with greater than or equal to 8 members, the 8-member ring having a window size of at least 2.5 Angstroms x at least 3.6 Angstroms and at least one Br.slzero.nsted acid site and the zeolite having a silica : X2O3 ratio of at least 5, wherein X is selected from aluminium, boron, iron, gallium and mixtures thereof with the proviso that the zeolite is not modernite or ferrierite.

Description

PROCESS FOR CARBONYLATION OF ALIPHATIC ALCOHOLS AND/OR
REACTIVE DERIVATIVES THEREOF.
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BACKGROUND OF THE INVENTION
[0001] This invention relates to a process for the selective production of lower aliphatic carboxylic acids and/or their corresponding esters by the carbonylation of the corresponding lower aliphatic alcohol and/or ester or ether derivatives thereof, and, in particularto the selective production of acetic acid and/or methyl acetate by the carbonylation of methanol and/or ester or ether derivatives thereof. This invention also relates to an improved process for the production of methyl acetate from dimethyl ether, and more generally to the production of alkyl esters of aliphatic carboxylic acids, by the carbonylation of alkyl ethers.
In another aspect this invention relates to the production of lower aliphatic carboxylic acids by first producing an alkyl ester from a lower alkyl ether, followed by hydrolysis of the ester to the acid. An example of this is the production of acetic acid by carbonylation of dimethyl ether, to form methyl acetate, followed by hydrolysis of the ester to produce acetic acid.

[0002] The most widely used industrial process for production of acetic acid is the carbonylation of methanol, which is described generally in British patents 1,185,453 and 1,277,242 and U.S. patent 3,689,533, for instance. In that type of process, methanol is reacted with carbon monoxide or a carbon monoxide- containing gas in the presence of a rhodium- or iridium-containing catalyst, in the additional presence of a halogen (usually iodine)-containing promoter. Though widely used, nonetheless these processes require the use of expensive corrosion-resistant alloys due to the presence of iodide and result in production of low levels of iodine-containing byproducts that are difficult to remove from the acetic acid by conventional distillation. Some non-halide based catalyst systems have been investigated for this reaction, but none have been commercialized, primarily due to issues with catalyst lifetime and selectivity.

[0003] A number of patents describe processes in which methanol or a mixture of methanol and dimethyl ether is carbonylated in the presence of a catalyst. Typically the products are a mixture of acetic acid and methyl acetate, sometimes also including acetic anhydride. In those patents it is disclosed that one of the reactions that may occur is the carbonylation of dimethyl ether to form methyl acetate.

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[0004] EP-A- 0 596 632 discloses the preparation of an aliphatic carboxylic acid by contacting an aliphatic alcohol or a reactive derivative thereof with carbon monoxide in the presence of a copper, nickel, iridium, rhodium or cobalt loaded mordenite zeolite catalyst at high temperatures and pressures.

[0005] WO 2005/105720 discloses a process for the preparation of an aliphatic carboxylic acid, ester or anhydride thereof by contacting an aliphatic alcohol and/or a reactive derivative thereof with carbon monoxide in the presence of a copper, nickel, iridium, rhodium or cobalt loaded mordenite catalyst which has as framework elements, silicon, aluminium and also one or more of gallium, boron and iron.
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[0006] US 6,387,842 discloses processes and catalysts for converting an alcohol, ether and/or ether alcohol feedstock to oxygenated products by reaction with carbon monoxide in the presence of a catalyst comprising a solid super acid, clay, zeolite or molecular sieve under conditions of temperature and pressure.

[0007] Cheung et al (Angew. Chem. Int. Ed 2006, 45, (10), 1617) carried out carbonylation of dimethyl ether with the zeolites mordenite, ferrierite and also with the zeolites ZSM-5, BEA and USY. These latter three zeolite types do not contain 8-member ring channels.
BRIEF SUMMARY OF THE INVENTION

[0008] This invention comprises a process for the selective production of a C1-C3 aliphatic carboxylic acid such as acetic acid and/or the corresponding C1-C3 ester, such as methyl acetate by carbonylating the corresponding C1-C3 aliphatic alcohol, such as methanol and/or an ester or ether derivative thereof, such as dimethyl ether with carbon monoxide in the presence of a catalyst comprising a zeolite, having at least one 8-member ring channel, said 8-member ring channel being interconnected with a channel defined by a ring with greater than or equal to 8 members, said 8-member ring having a window size of at least 2.5 Angstroms x at least 3.6 Angstroms and at least one Bronsted acid site and wherein the zeolite has a silica : X203 ratio of at least 5, wherein X is selected from aluminium, boron, iron, gallium and mixtures thereof, with the proviso that the zeolite is not mordenite or ferrierite.

[0009] .This invention also comprises a process for producing a product comprising a Ci-C3 alkyl ester of a C1-C3 aliphatic carboxylic acid, such as methyl acetate comprising carbonylating a C1-C3 alkyl ether, such as dimethyl ether with carbon monoxide under substantially anhydrous conditions in the presence of a catalyst comprising a zeolite having at least one 8-member ring channel, said 8-member ring channel being interconnected with a channel defined by a ring with greater than or equal to 8 members, said 8-member ring having a window size of at least 2.5 Angstroms x at least 3.6 Angstroms and at least one BrOnsted acid site and wherein the zeolite has a silica: X203 ratio of at least 5, wherein X is selected from aluminium, boron, iron, gallium and mixtures thereof, with the proviso that the zeolite is not mordenite or ferrierite.
DETAILED DESCRIPTION OF THE INVENTION

[0010] This invention comprises a process for the selective production of a C1-C3 aliphatic carboxylic acid such as acetic acid and/or the corresponding ester, such as methyl acetate by carbonylating the corresponding C1-C3 aliphatic alcohol, such as methanol and/or an ester or ether derivative thereof, such as dimethyl ether with carbon monoxide in the presence of a catalyst comprising a zeolite having at least one 8-member ring channel, said 8-member ring channel being interconnected with a channel defined by a ring with greater than or equal to 8 members, said 8-member ring having a window size of at least 2.5 Angstroms x at least 3.6 Angstroms and at least one Bronsted acid site and wherein the zeolite has a silica : X203 ratio of at least 5, wherein X is selected from aluminium, boron, iron, gallium and mixtures thereof, with the proviso that the zeolite is not mordenite or fenierite.

[0011] This invention also comprises a process for producing a product comprising a C1-C3 alkyl ester of a C1-C3 aliphatic carboxylic acid, such as methyl acetate comprising carbonylating a C1-C3 alkyl ether, such as dimethyl ether with carbon monoxide under substantially anhydrous conditions in the presence of a catalyst comprising a zeolite having at least one 8-member ring channel, said 8-member ring channel being interconnected with a channel defined by a ring with greater than or equal to 8 members, said 8-member ring ) having a window size of at least 2.5 Angstroms x at least 3.6 Angstroms and at least one BrOnsted acid site and wherein the zeolite has a silica: X203 ratio of at least 5, wherein X is selected from aluminium, boron, iron, gallium and mixtures thereof, with the proviso that the zeolite is not mordenite or ferrierite.
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[00121 In one aspect of the invention, one component of the feed to the process may be a C1-C3 aliphatic alcohol. The process is particularly applicable to alcohols such as methanol, ethanol and n-propanol. A preferred alcohol is methanol. Reactive derivatives of the alcohol which may be used as an alternative to, or in addition to the alcohol, include esters of the alcohol and ether derivatives of a C1-C3 alcohol. Suitable reactive derivatives of methanol include methyl acetate and dimethyl ether. A mixture of the alcohol and a reactive derivative thereof may also be employed, such as a mixture of methanol and methyl acetate.
[0013] Where an alcohol is used as the feed to the process, the product will be dependent upon the degree of conversion of the alcohol. If the conversion is 100% then the product will be the corresponding carboxylic acid. Thus where methanol is the alcohol feed, the product will comprise acetic acid. If the conversion is less than 100%, the alcohol will be converted to a mixture of the corresponding carboxylic acid and carboxylic acid ester. If the ester employed as the feed, is a symmetrical ester, for example, methyl acetate, the main product of the carbonylation process will be the corresponding carboxylic acid (in this case, acetic acid). If the ester is asymmetrical, then the product will comprise a mixture of carboxylic acids formed from each of the alkyl groups of the ester.
[0014] In a further aspect of the invention, one component of the feed to the process comprises a C1-C3 alkyl ether, that is, a compound having the formula in which R1 and R2 are independently C1-C3 alkyl groups. The total number of carbon atoms in groups R1 and R2, if R1 and R2 are alkyl groups, is from 2 to 6.
Preferably, R1 and R2 are straight-chain alkyl groups, most preferably straight-chain alkyl groups having from 1 to 3 carbon atoms each, such as methyl, ethyl and n-propyl.
[0015] If the ether is a symmetrical ether, for example, dimethyl ether, the main product will be the corresponding alkyl ester of an aliphatic acid (in this case, methyl acetate). If the ether is asymmetrical, the product will comprise one or both of the two possible carboxylic acid I esters, depending on which of the two C-0 bonds is cleaved in the reaction. For example, if the feed is methyl ethyl ether (R1 = methyl; R2 ethyl), then the product will comprise ethyl acetate and/or methyl propionate.
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[0016] A second component of the process is a feed comprising carbon monoxide.
The feed may comprise substantially pure carbon monoxide (CO), for example, carbon monoxide typically provided by suppliers of industrial gases, or the feed may contain impurities that do not interfere with the conversion of the alkyl ether to the desired ester, such as hydrogen, nitrogen, helium, argon, methane and/or carbon dioxide. For example, the feed may comprise CO that is typically made commercially by removing hydrogen from synthesis gas via a cryogenic separation and/or use of a membrane.
[0017] The carbon monoxide feed may contain substantial amounts of hydrogen.
For example, the feed may be what is commonly known as synthesis gas, i.e. any of a number of gaseous mixtures that are used for synthesizing a variety of organic or inorganic compounds, and particularly for ammonia synthesis. Synthesis gas typically results from reacting carbon-rich substances with steam (in a process known as steam reforming) or with steam and oxygen (a partial oxidation process). These gases contain mainly carbon monoxide and hydrogen, and may also contain smaller quantities of carbon dioxide and nitrogen. Suitably, the ratio of carbon monoxide : hydrogen may be in the range 1 : 3 to 15: 1 on a molar basis, such as 1: 1 to 10: 1. The ability to use synthesis gas provides another advantage over processes for producing acetic acid from methanol, namely the option of using a less expensive carbon monoxide feed. In methanol-to-acetic acid processes, the inclusion of hydrogen in the feed can result in production of unwanted hydrogenation.
[0018] The catalyst for use in the process of the invention is a zeolite, excluding mordenite and ferrierite. Zeolites, both natural and synthetic are microporous crystalline aluminosilicate materials having a definite crystalline structure as determined by X-ray diffraction. The chemical composition of zeolites can vary widely but they typically consist of Si02 in which some of the Si atoms may be replaced by tetravalent atoms such as Ti or Ge, by trivalent atoms such as Al, B, Ga, Fe or by bivalent atoms such as Be, or by a combination thereof. A
zeolite is comprised of a system of channels which may be interconnected with other channel systems or cavities such as side-pockets or cages. The channel systems are uniform in size 1 within a specific zeolite and may be three-dimensional but are not necessarily so and may be two-dimensional or one-dimensional. The channel systems of a zeolite are typically accessed via 12-member rings, 10-member rings or 8 member rings. The zeolites for use in the present invention contain at least one channel which is defined by an 8-member ring.
Preferred zeolites are those which, do not have side-pockets or cages within the zeolite structure. The Atlas of Zeolite Framework Types (C. Baerlocher, W. M. Meier, D. H. Olson, 5th ed. Elsevier, Amsterdam, 2001) in conjunction with the web-based version (http://www.iza-structure.org/databases/) is a compendium of topological and structural details about zeolite frameworks, including the types of ring structures present in the zeolite and the dimensions of the channels defined by each ring type. For the purposes of the present invention, the term 'zeolite' also includes materials having a zeolite-type structure such as delaminated porous crystalline oxide materials and pillared layered oxide materials such as ITQ-36.
[0019] The process of the present invention employs a zeolite having at least one channel defined by an 8-member ring of tetrahedrally co-ordinated atoms (tetrahedra) with a window size having a minimum dimension of 2.5 Angstroms x 3.6 Angstroms. The 8-member ring channel is interconnected with at least one channel defined by a ring with equal to or greater than 8 members, such as 10 and/or 12 members. The interconnected 8-, 10, and 12- member ring channels provide access to BrOnsted acid sites contained in the 8-member ring channels to enable the carbonylation of the C1-C3 alcohol or derivative thereof, such as methanol and dimethyl ether to proceed at acceptable rates.
[0020] The zeolite for use in the present invention may consist of interconnected channels defined solely by 8-member rings, such as zeolites of framework type CHA, for example, chabazite and framework type ITE,' for example ITQ-3. Preferably, however, the zeolite has at least one channel formed by an 8-member ring and at least one interconnecting channel defined by a ring with greater than 8 members, such as a 10, and/or 12 member ring. Non-limiting examples of zeolites having 8- member ring channels and interconnecting larger ring channel systems include zeolites of framework type OFF, for example, offretite, GME, for example Gmelinite, MFS, such as ZSM-57, EON such as ECR-1 and ETR such as ECR-34.
Preferably, the zeolites for use in the process of the present invention have at least one 8-member ring channel interconnected with at least one 12-member ring channel, such as those of framework type OFF and G1V1E, for example, offretite and gmelinite.
[0021] However, the mere presence of an interconnected 8-member ring channel in a zeolite is not sufficient to develop an effective carbonylation process. The window size of the channel systems also has to be controlled such that the reactant molecules can diffuse freely in and out of the zeolite framework. It has now been found that effective carbonylation can be achieved if the aperture (pore width) of an 8-member ring channel of the zeolite has a minimum dimension of 2.5 x 3.6 Angstroms. Channel dimensions of zeolite framework types may be found, for example, in the Atlas of Zeolite Framework Types. In addition, M.D.
Foster, I. Rivin, M.M.J. Treacy and 0. Delgado Friedrichs in "A geometric solution to the largest-free-sphere problem in zeolite frameworks" Microporous and Mesoporous Materials 90 (2006) 32-38, have used Delaunay triangulation methods applied to known zeolite frameworks and have tabulated the largest free-sphere diameters for diffusion along the three principal crystallographic directions for the 165 zeolite frameworks that are currently listed in the Atlas of Zeolite Framework Types. Ring window sizes may be modified by suitable atomic substitutions that change bond lengths and bond angles of the tetrahedrally co-ordinated atoms and the bridging oxygens.
[0022] A partial listing of zeolite framework types having at least one interconnected 8 member ring channel of minimum dimension of 2.5 x 3.6 Angstroms taken from The Atlas of Zeolite Framework Types is given below:
MOR Mordenite 12 (6.5 x 7.0A) 8 (3.4 x 4.8A) 8 (2.6 x 5.7A) OFF Offretite 12 (6.7 x 6.8A) 8 (3.6 x 4.9A) FER Ferrierite 10 (4.2 x 5.4A) 8 (3.5 x 4.8A) CHA Chabazite 8 (3.8 x 3.8A) 1TE ITQ3 8 (3.8 x 4.3A) 8 (2.7 x 5.8A) GME Gmelinite 12 (7.0 x 7.0A) 8 (3.6 x 3.9A) ETR ECR-34 18 (10.1A) 8 (2.5 x 6.0A) MFS ZSM-57 10 (5.1 x 5.4A) 8 (3.3 x 4.8A) EON ECR-1 12 (6.7 x 6.8A) 8 (3.4 x 4.9A) 8 (2.9 x 2.9A) [0023] Zeolites are available from commercial sources. Alternatively they may be synthesized using known techniques. In general, synthetic zeolites are prepared from aqueous reaction mixtures comprising sources of appropriate oxides. Organic directing agents may also be included in the reaction mixture for the purpose of influencing the production of a zeolite having the desired structure. After the components of the reaction mixture are properly mixed with one another, the reaction mixture is subjected to appropriate crystallization conditions. After crystallization of the reaction mixture is complete, the crystalline product may be recovered from the remainder of the reaction mixture. Such recovery may involve filtering the crystals, washing with water followed by a calcination treatment at high temperature. The synthesis of zeolites is described in numerous references.
For example, zeolite Y and its synthesis is described in US 3,130,007, zeolite ZSM-23 is described in US 4,076,842 and J.Phys. Chem. B, 109, 652-661 (2005), Zones, S.I. Darton, R.J., Morris, R and Hwany, S-J; ECR-18 is described in Microporous Mesoporous Mat., 28, 233-239 (1999), Vaughan D.E.W. & Strohmaier, K.G.; Theta-1 is described in Nature, 312, 533-534 (1984). Barn, S.A.I., Smith W.G., White, D and Young, D.; Mazzite is described in Microporous Mesoporous Mat., 63, 33-42 (2003), Martucci, A, Alberti, A, Guzmar-Castillo, M.D., Di Renzo, F and Fajula, F.; Zeolite L is described in Microporous Mesoporous Mat., 76, 81-99 (2004), Bhat, S.D., Niphadkair, P.S., Gaydharker, T.R., Awate, S.V., Belhekar, A.A. and Joshi, P.N and also in J. Ind. Eng. Chem. Vol. 10, No. 4 (2004), 636-644, Ko Y.S, Ahn W.S and offretite is described in Zeolites 255-264, Vol. 7, 1987 Howden M.G.
[0024] The zeolite catalyst for use in the process of the present invention is used in the acid form, generally referred to as the 'H' form of the zeolite, for example, FE-offretite. Other forms of the zeolite, such as the NH4 form can be converted to the H-form, for example, by calcining the NH4 form at elevated temperature. The acid form of a zeolite will possess BrOnsted acid (H+) sites which are distributed among the various channel systems in the zeolite. For example, H-offretite has 11+ sites located in the 12 member ring channels and in the 8 member ring channels. The number or concentration of 1-1+ species residing in any particular channel system can be determined by known techniques such.as infra-red NMR
spectroscopic techniques. Quantification of Bronsted acidity by FTIR and NNIR
spectroscopy is described, for example, in Makarova; M.A., Wilson, A.E., van Liemt, B.J., Mesters, C. de Winter, A.W., Williams, C. Journal of Catalysis 1997, 172, (1), 170. The two types of channels in H-offretite (defined by 12 member rings and 8 member rings) give rise to at least two bands associated with the hydroxyl region of H-offretite, one corresponding to vibration into the larger pores and the other, at a lower frequency, vibrating into the smaller pores. Work by the present inventors has shown that there is a correlation between the number of II+ sites located in an 8-member ring channel and the carbonylation rate whereas no such correlation has been observed for 12-member ring channels. It has been found that carbonylation rates increase in parallel with the number of El+ sites within 8 member ring channels. In contrast, no correlation is evident with the number of 11+ sites within 12 member ring channels. The number of Er sites within 8-member ring channels can be controlled by replacement of the 11 with metal cations such as Na + or Co2 using known ion-exchange techniques.

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[0025] The chemical composition of a zeolite may be expressed as involving the molar relationship:
Si02 : X203 wherein X is a trivalent element, such as aluminium, boron, iron and/or gallium, preferably aluminium. The Si02: X203 ratio of a given zeolite is often variable. For example, it is known that offretite can be synthesized with Si02: A1203 ratios of 6 to 90 or greater, zeolite Y, from about 1 to about 6, chabazite from about 2 to 2000 and gmelinite may be synthesised with Si02 : A1203 ratios of greater than 4. In general, the upper limit of the Si02 : X203 ratio is unbounded, for example, the zeolite ZSM-5. The zeolites for use in the present invention have a Si02 : X203 molar ratio of at least 5, preferably in the range 7 to 40, such as 10 to 30.
Suitably, the Si02 : X203 molar ratio is less than or equal to 100. Particular Si02: X203 ratios can be obtained for many zeolites by dealumination (where X is Al), by standard techniques using high temperature steam treatment or acid washing.
[0026] Depending on the nature of the feed, water may be generated in-situ.
For example, where an alcohol is used as the feed, water is generated by the dimerisation of the alcohol to an ether, Water may also be generated by the estenification of the alcohol with the carboxylic acid product. Water may be fed separately or together with the alcohol or ester feed component or a mixture thereof. The water may be present in liquid or vapour form. Where, the process of the present invention is carried out under hydrous conditions and the feed is an aliphatic alcohol or an aliphatic ester, the carbonylation reaction products will be the corresponding carboxylic acid and/or ester. For example, where the feed is methanol or methyl acetate, the reaction products will be acetic acid and/or methyl acetate. Where the feed is a C1-C3 alkyl ether, such as dimethyl ether the carbonylation reaction is preferably carried out under substantially anhydrous conditions. In the substantial absence of water, the carbonylation of dimethyl ether is selective to methyl acetate product.
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[0027] Where the reaction is to be conducted substantially in the absence of water, the catalyst and preferably, the feed components should be dried before beginning the operation, for example, by preheating to 400- 500 C.

[0028] In general, where the feed is an ether, such as dimethyl ether, the process is run at temperatures at or below about 250 C, that is, at temperatures of from about 100 to about 250 C, preferably from about 150 to about 180 C . Where the feed is an alcohol or an ester, such as methanol or methyl acetate, the process is run at temperatures above 250 C, that is, at temperatures of from about 250 to about 400 C, preferably from about 275 to about 350 C .
[0029] Typical total operating pressures are from about 1 bar to about 100 bar, preferably with carbon monoxide pressures greater than 10 bar and reactant pressures below 5 bar.
[0030] The process may be run as either a continuous or a batch process, with continuous processes typically preferred. 'Essentially, the process is a gas-phase operation, with reactants being introduced in either liquid or gaseous phase and products withdrawn as gases. As desired, the reaction products may subsequently be cooled and condensed. The catalyst may be used as convenient, in either a fixed bed or a fluidized bed. In operating the process, unreacted starting materials may be recovered and recycled to the reactor.
Where the product is methyl acetate it may be recovered and sold as such, or may be forwarded to other chemical process units as desired. If desired, the entire reaction product may be sent to a chemical process unit for conversion of the methyl acetate or acetic acid and optionally other components to other useful products.
[0031] In one preferred embodiment of the invention, where methyl acetate is a product, it may be recovered from the reaction products and contacted with water to form acetic acid via hydrolysis reactions. Alternatively, the entire product may be passed to a hydrolysis step, and acetic acid separated thereafter. The hydrolysis step may be carried out in the presence of an acid catalyst, and may take the form of a reactive distillation process, well known in the art.
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[0032] After separation, any alcohols produced in the reaction may be sent to a dehydration reactor to produce an ether, which can be separated from water and recycled to the carbonylation unit as fresh feed for the carbonylation reactor.
[0033] In another embodiment, the hydrolysis of an ester product to alcohol and carboxylic acid is performed by injecting water at one or more points in the catalyst bed, once a significant amount of ester has been produced by carbonylation. Injection of water in this manner essentially stops the conversion of, for example, dimethyl ether to methyl acetate, and removes the requirement for a separate hydrolysis reactor.
[0034] The following examples are presented as illustrative of the invention.
However, they are not meant to limit the scope of this invention General Procedures 1) Catalyst Preparation [0035] A catalyst sample in the ammonium or acid form was compacted at 12 tonnes in a 33 TM
mm die set using a Speedo' Press, then crushed and sieved to a particle size fraction of 212 to 335 microns. The catalyst (typically 1g) was then calcined to convert the N114+ form to 11+
form in a muffle oven (oven-volume = 30L) under a static atmosphere of air.
The temperature was increased from room temperature to 450 C at a ramp rate of 5 C/mm and then held at this temperature for 12 hours. Details of the zeolites are given in Table 1 below.
Table 1 Zeolite precursor Silica/Alumina Channel Structure Molar Ratio NH4-0ffretite-10 10 8 (3.6 x 4.9A) 12 (6.7 x 6.8A) =
NH4-Chabazite 7.3 8 (3.8 x 3.8A) NH4-ZSM-23 85 10(4.5 x 5.2A) NH4- ECR-18 7.8 8 (3.6 x 3.6A) 8 (3.6 x 3.6A) NH4-Theta-1 70 10 (4.6 x 5.7A) NH4- Zeolite "A 1.2 8 (4.1 x 4.1A) =
(Grace Davison) NH4-Zeolite L 14 12 (7.1 x 7.1A) H-Mazzite 7.7 8 (3.1 x 3.1A) 12 (7.4 x 7.4A) N114-BETA-18 18 12 (6.6 x 6.7A) (ZeolystTM International) 12 (5.6 x 5.6A) The sodium form of zeolite A was converted to the NH4+form by stirring 1 gram of material in a 10 ml solution of 1 molar ammonium nitrate for three hours and then filtering off the solution. This was repeated three times and the solid dried at 100 C in air before pressing and sieving. The N1L4+ exchanged NaA was not calcined prior to use.

Dimethvl Ether Carbonvlation Reaction [0036] Dimethyl ether carbonylation reactions were carried out in a pressure flow reactor unit consisting of 60 identical parallel isothermal co-current tubular reactors.
Into each tube 50 micro litres of catalyst was loaded onto a metal sinter having a pore size of 20 micrometers.
All catalyst samples were heated at a ramp rate of 5 C/ min. to 100 C under N2 at atmospheric pressure at a flow rate of 3.33 ml] hour, and held at this temperature for 1 hour.
The reactor was then pressurised to 70 barg with N2and the system held at this condition for 1. hour. The nitrogen gas feed was then changed to a mixture comprising 64 mole % carbon monoxide, 16 mole % hydrogen and 20 mole % nitrogen at a gas flow rate of 3.33 ml/ hour, and the system were heated at a ramp rate 3 C/ min. to a temperature of 300 C. The system was then held at this condition for 3 hours. After this the temperature was reduced to 180 C
and allowed to stabilise for 10 minutes. At this point catalyst activation is considered complete and the gas feed was changed to a mixture comprising 64 mole % carbon monoxide, 16 mole % hydrogen, 15 mole % nitrogen and 5 mole % dimethyl ether at a gas flow rate of 3.33 ml/ hour. The reaction was allowed to continue for 27.8 hours after which the temperature was increased to 250 C. The exit stream from the reactor was passed to a TM
Varian 4900 micro gas chrornatograph with three columns (Molecular Sieve 5A, Porapake Q
TM
and CP-Wax-52) each column being equipped with a thermal conductivity detector; and an Interscience Trace gas chromatograph having two columns (CP-Sil 5 and CP-Wax 52) each equipped with a flame ionization detector. The results of the carbonylation reactions are given in Table 2.

Table 2 Example Catalyst Reaction Time on STYmeoAc temperature Stream /hrs grlh-1 1. NI-14-Offretite-i0 180 19.6 55 2. _ 250 48.8 3. NH4-Chabazite 180 19.7 4. 250 49.0 0 5. NH4-ZSM-23 180 21.2 6. 250 50.4 4 7. NH4-ECR-18 180 16.0 8. 250 50.8 1 9. NH4-Theta-1 180 17.3 10. 250 52.1 1 11. Na-Zeolite A 180 21.4 12. 250 50.6 0 13. NH4-Zeolite L 180 20.3 14. 250 49.5 0 15. H-Mazzite 180 20.7 1.

16. 250 49.9 6 17. NH4-BETA-18 180 16.2 1 18. 250 51.0 2 [0037] In the above experiments, the offretite, chabazite, and ECR-18 zeolites have a silica:
alumina molar ratio of at least 5, an 8-member ring channel of window size of at least 2.5 Angstroms x at least 3.6 Angstroms and at least one Bronsted acid site, and.the 8-member ring channel is interconnected with a channel defined by a ring with greater than or equal to 8 members. These experiments demonstrate that significant carbonylation activity may be achieved by these zeolites. However, in the carbonylation reactions employing the zeolites, ZSM-23, Theta-1, Zeolite-A, Zeolite-L, Mazzite and Beta-18, little, if any carbonylation activity was found to occur. ZSM-23,and Theta-1 possess 10-member ring channels only and do not have 8-member ring channels; Beta-18 and Zeolite-L have 12-member ring channels only and does not have 8-member ring channels; the Zeolite-A has 8- member ring channels but its silica/alumina ratio is below 5; Mazzite has both 8- and 12-member ring channels but the 8-member ring channels do not intersect with either 8-member ring channels or 12-member ring channels. =
General Procedures B
[0038] To investigate the catalytic activity of zeolites for non-iodide carbonylation of methanol to acetic acid the zeolites can be tested in a pressure flow reactor in accordance with the following procedure. Zeolite pellets of size 500-1000um are loaded into a pressure flow reactor. A catalyst pre-bed is also employed to ensure efficient mixing/heating of the reactants. The pre-bed is gamma-alumina which allows methanol to form a methanol/dimethylether/water equilibrium. The catalysts are activated under flowing nitrogen (100cm3/min) at 350 C for 16hrs and then reduced under carbon monoxide (200cm3/min) at .350 C for 2 hours. The system is then pressurised up to 30barg using a back pressure regulator. The flow rate of the carbon monoxide is adjusted to 400cm3/min(GHSV=2200) and methanol is fed to the reactor via a pump (rate+0.15m1imin). The liquid products and unconverted reactants are collected in a cooled trap, while gaseous products and un-reacted feeds are sampled downstream by an online gas chromatograph. The reaction is sampled at frequent intervals and the liquid products analysed off line using gas-chromatography. Using zeolite H-Offretite (silica: alumina molar ratio of 10) as the catalyst in the above described carbonylation of methanol, it would be expected that significant amounts of both methyl acetate and acetic acid would be seen in the liquid products. Similarly, if zeolite H-Gmelinitc (silica: alumina molar ratio of 8) was employed as the catalyst in the above described carbonylation of methanol, it would be expected that significant amounts of both methyl acetate and acetic acid would be seen in the liquid products. Both offretite and gmelinite zeolites have 8-member ring channels intersecting with 12-member ring channels. In comparison, it would be expected that if zeolite H-ZSM-5 (silica: alumina ratio of 23; 10-member ring channels only) or zeolite H-Y (silica: alumina ratio of 12; 12-member ring channels only) were employed as the catalyst, only trace amounts of acetic acid would be seen in the liquid product.
[0039] Although the foregoing invention has been described in some detail by way of illustration and example for purposes of clarity of understanding, it will be readily apparent to those of ordinary skill in the art in light of the teachings of this invention that certain changes and modifications may be made thereto without departing from the scope of the appended claims.

Claims (42)

1. A process for the production of a C1-C3 aliphatic carboxylic acid and/or the corresponding ester, by carbonylating the corresponding C1-C3 aliphatic alcohol and/or an ester or ether derivative thereof with carbon monoxide in the presence of a catalyst comprising a zeolite having at least one 8-member ring channel, said 8-member ring channel being interconnected with a channel defined by a ring with greater than or equal to 8 members, said 8-member ring having a window size of at least 2.5 Angstroms x at least 3.6 Angstroms and at least one Br.slzero.nsted acid site and which zeolite has a silica : X2O3 molar ratio of at least 5, wherein X is selected from the group consisting of aluminium, boron, iron, gallium and mixtures thereof with the proviso that the zeolite is not mordenite or ferrierite.

2. A process according to claim 1, in which the C1-C3 carboxylic acid is acetic acid.

3. A process according to claim 1, in which the ester of the C1-C3 carboxylic acid is methyl acetate.

4. A process according to claim 1, wherein the C1-C3 alcohol is methanol or ethanol.

5. A process according to claim 4, wherein the alcohol is methanol.

6. A process according to claim 1, wherein an ether is carbonylated.

7. A process according to claim 6, wherein the ether is dimethyl ether.

8. A process according to claim 1, in which an ether is carbonylated at a temperature from about 100 °C to about 250 °C.

9. A process according to claim 1, in which an ether is carbonylated at a temperature from about 150 °C to about 180 °C.

10. A process according to claim 8 or 9, in which the ether is dimethyl ether.

11. A process according to claim 1, in which the alcohol or ester derivative thereof is carbonylated at a temperature from about 250 °C to about 400 °C.

12. A process according to claim 1, in which the alcohol or ester derivative thereof is carbonylated at a temperature from about 275 °C to about 350 °C.

13. A process according to claim 11 or 12, in which the alcohol is methanol and the ester derivative is methyl acetate.

14. A process according to any one of claims 1 to 13, in which the catalyst comprises a fixed bed of catalyst.

15. A process according to any one of claims 1 to 13, in which the catalyst comprises a fluidized bed of catalyst.

16. A continuous process according to any one of claims 1 to 15.

17. A batch process according to any one of claims 1 to 15.

18. A process according to any one of claims 1 to 17, in which the carbon monoxide is provided to the process in the form of a carbon monoxide-containing feed further comprising hydrogen.

19. A process according to claim 18, in which the carbon monoxide-containing feed comprises a synthesis gas.

20. A process according to claim 1, wherein the derivative of the alcohol is a C1-C3 ether and the process is carried out under substantially anhydrous conditions and the product is the corresponding ester.

21. A process according to claim 20, wherein the ether is dimethyl ether and the process is carried out under substantially anhydrous conditions and the product is methyl acetate.

22. A process according to claim 20, comprising further hydrolyzing the ester to produce the corresponding carboxylic acid.

23. A process according to claim 21, comprising further hydrolyzing the methyl acetate to produce acetic acid.

24. A process according to claim 22 or 23, in which the hydrolysis is conducted in a separate reactor from the ester-producing reaction.

25. A process according to claim 22 or 23, in which the hydrolysis is conducted in the same reactor as the ester-producing reaction.

26. A process according to any one of claims 1 to 25, in which the zeolite catalyst is selected from the group consisting of a zeolite of framework type OFF, CHA, ITE, GME, ETR, EON, and MFS.

27. A process according to claim 26, wherein the catalyst is selected from the group consisting of offretite, gmelinite, ZSM-57 and ECR-18.

28. A process according to claim 27, wherein the zeolite is offretite.

29. A process according to any one of claims 1 to 25, wherein the catalyst consists of channels defined solely by 8-member rings.

30. A process according to any one of claims 1 to 25, wherein the channel defined by the 8-member ring interconnects with at least one channel defined by a ring with greater than 8 members.

31. A process according to claim 30, wherein the at least one channel defined by a ring with greater than 8 members is defined by a ring having 10 or 12 members.

32. A process according to claim 31, wherein the at least one channel defined by a ring with greater than 8 members is defined by a ring having 12 members.

33. A process according to any one of claims 1 to 19, wherein the process is carried out under hydrous conditions.

34. A process according to claim 33, wherein water is fed separately or together with the alcohol and/or ester thereof

35. A process according to any one of claims 1 to 34, wherein the silica :

ratio is less than or equal to 100.

36. A process according to claim 35, wherein the silica : X2O3 ratio is in the range 7 to 40.

37. A process according to claim 36, wherein the silica : X2O3 ratio is in the range 10 to 30.

38. A process according to any one of claims 1 to 25 and 29 to 37, wherein X is selected from the group consisting of aluminium, gallium and mixtures thereof

39. A process according to claim 1, wherein X is aluminium.

40. A process according to any one of claims 1 to 34, wherein X is aluminium and the silica : Al2O3 ratio is less than or equal to 100.

41. A process according to claim 40, wherein the silica : Al2O3 ratio is in the range 7 to 40.

42. A process according to claim 41, wherein the silica : Al2O3 ratio is in the range 10 to 30.