Catalyst and use thereof in the production of vinyl acetate

Details Catalyst and use thereof in the production of vinyl acetate Catalyst and use thereof in the production of vinyl acetate

2001-03-27

2002-10-29

Hendrickson, Stuart L. (Department: 1754)

Organic compounds -- part of the class 532-570 series

Organic compounds

Carboxylic acid esters

C560S243000, C560S245000

Reexamination Certificate

active

06472556

ABSTRACT:

BACKGROUND OF THE INVENTION
The present invention relates to a process for the production of vinyl acetate and to a novel catalyst for use in the process.
Vinyl acetate is generally prepared commercially by contacting acetic acid and ethylene with molecular oxygen in the presence of a catalyst active for the production of vinyl acetate.
The catalyst suitable for use in the production of vinyl acetate may comprise a Group VIII metal, for example palladium, an alkali metal acetate promoter, for example sodium or potassium acetate, and an optional co-promoter, for example cadmium acetate or gold. In particular U.S. Pat. No. 5,185,308 discloses a process for preparing vinyl acetate by the catalytic oxidation of ethylene in the presence of acetic acid. The catalyst used is a supported palladium catalyst promoted with gold and potassium acetate.
Acetic acid, useful as a feedstock for the production of vinyl acetate, may be prepared by several methods as commonly practiced in the industry, for example by the liquid phase carbonylation of methanol and/or a reactive derivative thereof in the presence of a Group VIII noble metal catalyst, an alkyl iodide promoter and a finite concentration of water. The acetic acid produced is then used as a reactant in the production of vinyl acetate. The process, thus tends to be a two stage process.
U.S. Pat. No. 3,373,189 relates to a process for the production of vinyl acetate from ethylene and oxygen using a palladium catalyst. U.S. Pat. No. 4,188,490 discloses a process for the production of acetic acid and vinyl acetate using a palladium catalyst on a zinc oxide support. U.S. Pat. No. 3,637,818 discloses a process for the production of acetaldehyde, acetic acid and vinyl acetate by the oxidation of ethylene in the presence of a noble metal and manganese or cobalt oxides. The aforementioned processes are carried out in the liquid phase.
DESCRIPTION OF THE INVENTION
We have now found that vinyl acetate can be produced directly from a reactant mixture comprising ethylene, optionally water, and an oxygen-containing gas without the need to initially produce acetic acid as a separate stage in the overall process Through the use of a modified palladium catalyst, vinyl acetate can be produced directly in a one stage process.
Accordingly, the present invention provides a process for the production of vinyl acetate which comprises reacting ethylene with an oxygen-containing gas, and optionally water, in the presence of a catalyst comprising (1) a catalyst support, (2) palladium, (3) an acid, (4) at least one acetic acid catalyst promoter and (5) at least one vinyl acetate catalyst promoter and/or co-promoter.
In a further embodiment of the present invention there is provided a catalyst for use in the production of vinyl acetate which comprises (1) a catalyst support, (2) palladium, (3) an acid, (4) at least one acetic acid catalyst promoter and (5) at least one vinyl acetate catalyst promoter and/or co-promoter.
The present invention provides a novel and cost effective route for the production of vinyl acetate. The process is not only highly selective towards the production of vinyl acetate but does not require the independent and separate production of acetic acid which is then used as a co-reactant in the process. In contrast, use of the modified palladium catalyst results in the in-situ oxidation of the reactants to produce acetic acid which is then oxidised with ethylene to vinyl acetate. The bi-functional nature of the catalyst results in a direct process.
The present invention provides a process for the production of vinyl acetate from ethylene, an oxygen-containing gas and optionally water. The ethylene may be substantially pure or may be admixed with one or more of nitrogen, methane, ethane, carbon dioxide, hydrogen, and low levels of C
3
/C
4
alkenes or alkanes.
The oxygen-containing gas may be air or a gas richer or poorer in molecular oxygen than air. Suitably, the gas may be oxygen diluted with a suitable diluent, for example nitrogen or carbon dioxide. Preferably, the oxygen-containing gas is oxygen.
Water may be optionally co-fed into the reaction chamber. Where water is present in the reaction chamber, it may be present in an amount up to 50 volume percent, preferably in the range from 10 to 30 volume percent.
A small amount of acetic acid may also be introduced into the reaction chamber. Suitably, the acetic acid may be introduced through a recycle stream. Where it is desired to introduce acetic acid, this may be present in an amount up to 50 volume percent, preferably in the range from 5 to 20 volume percent.
The catalyst of the present invention comprises palladium. The palladium concentration may be greater than 0.5% by weight, preferably greater than 1% by weight based upon the total weight of the catalyst. The palladium concentration may be as high as 10% by weight for fixed bed or fluid bed applications.
The catalyst of the present invention is a supported catalyst. Suitable catalyst supports may comprise porous silica, alumina, silica/alumina, titania, zirconia or carbon. Preferably, the support is silica. Suitably, the support may have a pore volume from 0.2 to 3.5 ml per gram of support, a surface area of 5 to 800 m
2
per gram of support and an apparent bulk density of 0.3 to 1.5 g/ml. For catalysts used in fixed bed processes, the support typically has dimensions of 3 to 9 mm and may be spheric, tablet, extrudate, pill shaped or any suitable shape. For catalysts used in fluid bed processes, the support typically may have a particle size distribution such that at least 60% of the catalyst particles have a particle diameter of below 200 microns, preferably at least 50% less than 105 microns and no more than 40% of the catalyst particles have a diameter of less than 40 microns.
The catalyst composition comprises at least one acetic acid catalyst promoter. Suitable promoters include selenium, titanium, tellurium and/or vanadium-containing compounds. Preferably, the acetic acid catalyst promoter is an oxide, acetate or acetylacetonate of at least one of the aforementioned metals. Preferably, the acetic acid catalyst promoter content of the final catalyst is up to 10% by weight.
In addition to the palladium compound and the acetic acid promoter, the catalyst comprises at least one vinyl acetate catalyst promoter and/or co-promoter, preferably both a promoter and a co-promoter. Suitable promoters include gold, copper and/or nickel, and cadmium acetate. A preferred promoter is gold. Suitable sources of gold include gold chloride, tetrachloroauric acid HAuCl
4
, NaAuCl
4
, KAuCl
4
, dimethyl gold acetate, barium acetoaurate or gold acetate. The preferred gold compound is HAuCl
4
. The metal may be present in an amount of from 0.1 to 10% by weight in the finished catalyst. Suitable co-promoters include alkali or alkaline earth metal salts, preferably an acetate salt, such as potassium or sodium acetate. Preferably, the co-promoter content in the final catalyst is in the range from 0.1 to 9.5% by weight as acetate. A preferred catalyst component (5) is gold and either sodium or potassium acetate.
The catalyst composition comprises an acid. Preferably, the acid is a strong acid. Suitable acids comprise heteropolyacids which may include silicotungstic acid, phosphotungstic acid, phosphomolybdic acid, silicomolybdic acid, tungstomolybdophosphoric acid, tungstomolybdosilisic acid, tungstovanadophosphoric acid, tungstovanadosilisic acid, molybdovanadophosphoric acid, molybdovanadosilisic acid, borotungstic acid, boromolybdic acid, tungstomolybdoboric acid, molybdoaluminic acid, tungstoaluminic acid, molybdotungstoaluminic acid, molybdogermanic acid, tungstogermanic acid, molybdotungstogermanic acid, molybdotitanic acid, tungstotitanic acid, molybdotungstotitanic acid, cericmolybdic acid,cerictungstic acid, cericmolybdotungstic acid, molybdocobalt acid, tungstocobalt acid, molybdotungstocobalt acid, phosphoniobic acid, siliconiobic acid and silicotantalic acid. Among them, silicotungstic acid, phosphotungstic acid, phosphomolybdic acid, silico

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