Organic compounds -- part of the class 532-570 series – Organic compounds – Carboxylic acids and salts thereof
Reexamination Certificate
2002-11-13
2004-07-06
Raymond, Richard L. (Department: 1624)
Organic compounds -- part of the class 532-570 series
Organic compounds
Carboxylic acids and salts thereof
C562S416000, C562S417000, C568S431000
Reexamination Certificate
active
06759550
ABSTRACT:
This invention relates to an improved method for carrying out an oxidation reaction of an alkyl substituted aromatic compound to its corresponding aromatic acid. In particular the invention pertains to carrying out the oxidation reaction in an aqueous medium under pH control, wherein the aqueous medium preferably contains surfactant and preferably a low molecular weight material containing a polar end group as a co-surfactant.
The oxidation reactions of alkyl substituted aromatic compounds to their aromatic acid counterparts are well-known and industrially important reactions. These reactions typically involve contacting the alkyl substituted aromatic precursor with oxygen or an oxygen containing gas, in the presence of a catalyst or catalyst system, typically Mn (II), Co (II), and Br. These reactions have historically been carried out in a solvent composed primarily of organic acids, such as acetic acid or benzoic acid. It would be desirable to use a less expensive, less flammable, less aggressive and more environmentally benign solvent, such as water.
Many aromatic acid precursors are not soluble to any great extent in water, however, leading to difficulties in dispersing the organic phase in the aqueous medium. Poor dispersal of the starting material leads to problems such as reduced yields and reaction rates, and increased byproduct formation, compared to the same reaction run in the more traditional solvent.
Earlier attempts at substituting water for the organic acid solvents typically used in such reactions, including U.S. Pat. Nos. 4,258,209 and 4,218,810 which employ at least five percent by weight together with an organic acid as the solvent. These patents do not use bromine and teach that more catalyst is needed with greater amounts of water. Acid yields reported were relatively low, and expensive processing of the acid product is required. U.S. Pat. No. 4,323,699 employs an aqueous medium and an iodine promoter. Low yields and large amounts of by-product are again reported.
U.S. Pat. No. 4,892,970 teaches a staged process for the oxidation of substituted benzenes, wherein the bromine concentration is increased in the second stage. The second stage of the process is used to increase the yield and reduce the amount of by products otherwise seen in oxidation reactions carried out in an aqueous medium.
Having recognized that the problems with yield and by-product formation were a result of aromatic precursors not being soluble to any great extent in water, the present inventors sought to improve the dispersability of the hydrophobic starting materials. It was discovered that the oxidation reaction does not proceed well if not carried out at a relatively low pH. It was also discovered that surfactants, such as amphiphilic organic compounds like stearic acid or an &agr;-olefin sulfonate or sulfonate salt, could be advantageously used to improve the dispersability of the hydrophobic starting materials. It is believed that the surfactants enhance the dispersion of an aromatic precursor in the aqueous liquid medium. Further, it was discovered that a co-surfactant comprising a low molecular weight polar organic material (such as 1-butanol, toluic acid or benzoic acid) in combination with the surfactant, can contribute greatly to the efficiency of the surfactant in this dispersion process.
Accordingly, the present invention relates to a method for oxidizing substituted aromatic compounds to their corresponding aromatic acids, comprising dispersing the substituted aromatic compound in a liquid medium, contacting the substituted aromatic compound with oxygen or an oxygen-containing gas in the presence of a catalyst, wherein the liquid medium comprises at least 30 per cent by weight (based on the total amount of the feed reaction mixture) water and optionally up to 30 per cent by weight surfactant, and wherein the reaction mixture is at a pH lower than 3.0.
The general reaction materials and conditions which are suitable for this invention (other than the liquid medium) are any of those known in the art {see, for example. Kirk-Othmer Encyclopedia of Chemical Technology, 4
th
Ed, Vol. 18, p. 1006). Accordingly, the starting material can be any substituted aromatic compound having at least one substituent group which is capable of being oxidized to a carboxylic acid or derivative. This includes alkyl, hydroalkyl, aldehyde, hydroxyalkyl, and carboalkyl groups. Of particular importance are the di-alkyl-substituted benzene derivatives, such as meta and para-xylene, and dimethyl naphthalene.
Similarly, the catalyst system can be any of those known in the art for use in oxidation reactions of substituted aromatic compounds. See, for example W. Partenheimer, Catalysis Today, 23 (1995); U.S. Pat. No. 5,359,133; U.S. Pat. No. 5,112,992; and WO 98/29378. Preferred catalysts include manganese (II) and at least one additional metal selected from the group consisting of cobalt, nickel, chromium, zirconium, hafnium, cerium, palladium, and mixtures thereof. It is preferred that the second metal be selected from the group consisting of cerium, cobalt, hafnium and zirconium. A bromine-affording material (which may be elemental bromine, a bromide or bromate salt, hydrobromic acid, a bromine substituted organic compound, or a mixture thereof is also advantageously added, as is known in the art. The catalyst can be added to the liquid before, after or together with the to substituted aromatic compound. The amount of catalyst components used is within the ranges known in the art. For the purposes of the present invention the bromine concentration (as bromine element or ion) in the total feed reaction mixture is in the range of 100 to 10000 ppm w/w, preferably in the range of 500 to 6000, most preferably in the range of 1000 to 4000. The ratio bromine to metals is in the range of from 0.8 to 6, preferably in the range of 1 to 4, most preferably in the range of 1.5 to 3. The ratio Mn to additional metal is in the range of 0.5 to 4, preferably in the range of 1 to 3.
The oxygen-containing gas supplied to the reactor can be pure oxygen, air, oxygen-enriched air or a mixture of oxygen with an inert gas, and can be added to the reactor by any method known in the art.
The liquid medium comprises at least 30 percent by weight water. It has been discovered that the oxidation reaction, when conducted using as reaction medium only water, does not proceed well (low yield, low rate and low product purity) when the pH of the reaction medium is higher than 3.0. Therefore, the pH of the reaction mixture should be less than 3.0 preferably less than 2.5, most preferably less than 2.0. It is preferred that an acid such as acetic acid, methanesulfonic acid, or sulfuric acid, or others, be added to the aqueous medium in an amount sufficient to bring the pH of the reaction mixture to the desired level. It is preferred that an amount of surfactant, up to 30 per cent by weight based on the total feed reaction mixture, also be added to the reaction mixture. A low molecular weight molecule containing a hydrophilic end group, or “co-surfactant” should also be present to increase the efficiency of the surfactant. It is preferred that the co-surfactant have a molecular weight less than 1000. The co-surfactant can advantageously be a by product or intermediate in the oxidation reaction of the substituted aromatic compound. For example, in the oxidation of xylenes to the corresponding phthalic acids, preferred co-surfactants include benzoic, toluic and acetic acid. The co-surfactant is preferably present in a concentration of from 0.1 to 10 percent by weight based on the total amount of the feed reaction mixture including any co-surfactant which may be generated in the oxidation reaction. It should be noted that the co-surfactant is preferably an acid, and this helps to bring the pH to the preferred levels.
The water content is preferably in the range of from 30 to 95 percent, most preferably in the range of from 50 to 85 percent. The surfactant concentration, including any co-surfactant used, depends on the surfactant speci
Burdett Kenneth A.
Green Daniel Patrick
Kalantar Thomas H.
Klier John
Lee Guo-shuh John
Raymond Richard L.
The Dow Chemical Company
Tucker Zachary
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