Terephthalic acid

History

Terephthalic acid was first isolated (from turpentine) by the French chemist Amédée Cailliot (1805–1884) in 1846. Terephthalic acid became industrially important after World War II. Terephthalic acid was produced by oxidation of p-xylene with 30-40% nitric acid. Air oxidation of p-xylene gives p-toluic acid, which resists further air-oxidation. Esterification of p-toluic acid to methyl p-toluate (CH3C6H4CO2CH3) opens the way for further oxidation to monomethyl terephthalate. In the Dynamit−Nobel process these two oxidations and the esterification were performed in a single reactor. The reaction conditions also lead to a second esterification, producing dimethyl terephthalate, which could be hydrolysed to terephthalic acid. In 1955, Mid-Century Corporation and ICI announced the bromide-catalysed oxidation of p-toluic acid directly to terephthalic acid, without the need to isolate intermediates and still using air as the oxidant. Amoco (as Standard Oil of Indiana) purchased the Mid-Century/ICI technology, and the process is now known by their name.

Synthesis

Amoco process

In the Amoco process, which is widely adopted worldwide, terephthalic acid is produced by catalytic oxidation of p-xylene: :[[Image:Oxidation p xylene.svg|200px|Terephthalic acid]] The process uses a cobalt–manganese–bromide catalyst. The bromide source can be sodium bromide, hydrogen bromide or tetrabromoethane. Bromine functions as a regenerative source of free radicals. Acetic acid is the solvent and compressed air serves as the oxidant. The combination of bromine and acetic acid is highly corrosive, requiring specialized reactors, such as those lined with titanium. A mixture of p-xylene, acetic acid, the catalyst system, and compressed air is fed to a reactor.

Mechanism

The oxidation of p-xylene proceeds by a free radical process. Bromine radicals decompose cobalt and manganese hydroperoxides. The resulting oxygen-based radicals abstract hydrogen from a methyl group, which have weaker C–H bonds than does the aromatic ring. Many intermediates have been isolated. p-xylene is converted to p-toluic acid, which is less reactive than the p-xylene owing to the influence of the electron-withdrawing carboxylic acid group. Incomplete oxidation produces 4-carboxybenzaldehyde (4-CBA), which is often a problematic impurity.

:[[File:Oxidation of p-xylene to terephthalic acid.svg|600px|Oxidation of p-xylene to TPA]]

Challenges

Approximately 5% of the acetic acid solvent is lost by decomposition or "burning". Product loss by decarboxylation to benzoic acid is common. The high temperature diminishes oxygen solubility in an already oxygen-starved system. Pure oxygen cannot be used in the traditional system due to hazards of flammable organic–O2 mixtures. Atmospheric air can be used in its place, but once reacted needs to be purified of toxins and ozone depleters such as methylbromide before being released. Additionally, the corrosive nature of bromides at high temperatures requires the reaction be run in expensive titanium reactors.

Alternative reaction media

The use of carbon dioxide overcomes many of the problems with the original industrial process. Because CO2 is a better flame inhibitor than N2, a CO2 environment allows for the use of pure oxygen directly, instead of air, with reduced flammability hazards. The solubility of molecular oxygen in solution is also enhanced in the CO2 environment. Because more oxygen is available to the system, supercritical carbon dioxide (Tc = 31 °C) has more complete oxidation with fewer byproducts, lower carbon monoxide production, less decarboxylation and higher purity than the commercial process.

In supercritical water medium, the oxidation can be effectively catalyzed by MnBr2 with pure O2 in a medium-high temperature. Use of supercritical water instead of acetic acid as a solvent diminishes environmental impact and offers a cost advantage. However, the scope of such reaction systems is limited by the even more demanding conditions than the industrial process (300–400 °C, 200 bar).

Promotors and additives

As with any large-scale process, many additives have been investigated for potential beneficial effects. Promising results have been reported with the following.

• Ketones act as promoters for formation of the active cobalt(III) catalyst. In particular, ketones with α-methylene groups oxidize to hydroperoxides that are known to oxidize cobalt(II). 2-Butanone is often used.
• Zirconium salts enhance the activity of Co-Mn-Br catalysts. Selectivity is also improved.
• N-Hydroxyphthalimide is a potential replacement for bromide, which is highly corrosive. The phthalimide functions by formation of the oxyl radical.
• Guanidine inhibits the oxidation of the first methyl but enhances the usually slow oxidation of the toluic acid.

Alternative routes

Terephthalic acid can also be made from toluene by the Gattermann-Koch reaction, which gives 4-methylbenzaldehyde. Oxidation of the latter gives terephthalic acid.

Terephthalic acid can be prepared in the laboratory by oxidizing many para-disubstituted derivatives of benzene, including caraway oil or a mixture of cymene and cuminol with chromic acid.

Although not commercially significant, there is also the so-called "Henkel process" or "Raecke process", named after the company and patent holder, respectively. This route involves the transfer of carboxylate groups. Either potassium benzoate disproportionates to potassium terephthalate and benzene or potassium phthalate rearranges to the terephthalate. Phthalic anhydride can be used as a raw material and then potassium can be recycled.

Applications

Virtually the entire world's supply of terephthalic acid and dimethyl terephthalate are consumed as precursors to polyethylene terephthalate (PET). A smaller, but nevertheless significant, demand for terephthalic acid exists in the production of polybutylene terephthalate and several other engineering polymers. Kevlar is a polyamide derived from terephthalic acid. Poly(ester amide)s are another class of polymers that have novel properties.

Other uses

• As a raw material to make plasticizers such as dioctyl terephthalate and dibutyl terephthalate.
• In the pharmaceutical industry as a raw material for certain drugs.
• As a popular component for the synthesis of metal-organic frameworks.
• To form terepthalate salts of certain drug freebases, such as oxycodone.
• As the primary obscurant in some military smoke grenades, most notably the American M83 smoke grenade and M90 vehicle-employed smoke grenade, producing a thick white smoke (the result of vaporized terepthalic acid recondensing). It acts as an obscurant in the visual and near-infrared spectrum.

Biodegradation

In Comamonas thiooxydans strain E6, terephthalic acid is biodegraded to protocatechuic acid, a common natural product, via a reaction pathway initiated by terephthalate 1,2-dioxygenase. Combined with the previously known PETase and MHETase, a full pathway for PET plastic degradation can be engineered.

References

References

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