Liquid purification or separation – Processes – Liquid/liquid solvent or colloidal extraction or diffusing...
Reexamination Certificate
1996-05-01
2002-03-19
Vargot, Mathieu D. (Department: 1732)
Liquid purification or separation
Processes
Liquid/liquid solvent or colloidal extraction or diffusing...
C210S806000, C210S908000, C210S909000, C210SDIG005
Reexamination Certificate
active
06358419
ABSTRACT:
This Application claims the priority of German Application P 43 21 513.0, filed Jun. 29, 1993.
The invention relates to the purification of wastewater which is produced from the aldolization of identical or different aldehydes or ketones, as well as from the aldolization of a mixture of aldehydes and ketones. The aim of the novel process is to reduce the COD (chemical oxygen demand) value of the wastewater.
BACKGROUND OF THE INVENTION
The term aldolization as used herein includes both the aldol addition and the aldol condensation reactions. The acidic or base catalyzed addition reaction of activated methylene groups onto the carbonyl groups of aldehydes or ketones, with formation of &bgr;-hydroxycarbonyl compounds, is termed aldol addition. If elimination of water follows the aldol addition (which occurs readily and is the rule when acid catalysts are used), the reaction is termed aldol condensation. Its products are &agr;,&bgr;-unsaturated carbonyl compounds.
The aldolization of two molecules of the identical aldehyde or identical ketone is of particular importance. An example of the industrial application of aldolization is the preparation from n-butyraldehyde of 2-ethylhexanol, which is, after the lower alcohols (methanol to butanol), the most important synthetic alcohol. Phthalic esters of 2-ethylhexanol are extensively used as plasticizers. To obtain the alcohol, n-butyraldehyde is converted into 2-ethylhexenal in the presence of an aqueous sodium hydroxide solution. After separating the aldolization mixture, the unsaturated aldehyde is washed with water and hydrogenated to give the desired alcohol.
In the course of the process, there are produced, as wastewater, the spent aqueous catalyst solution, the wash water used for purification of the 2-ethylhexanol, and water-containing residues of the 2-ethylhexanol distillation. The combined wastewater contains all the water-soluble impurities which occur in the individual process stages, including high proportions of organic compounds, such as butanol, butyric acid, butyrolactone, 2-ethylhexenal, and higher-boiling condensation products. Their concentration is conventionally indicated by the COD value. The COD value is the amount of potassium dichromate, expressed as oxygen equivalent, which is consumed by the oxidizable constituents of one liter of wastewater. It is determined by a standardized procedure described in, e.g., Ullmanns Encyclopädie der technischen Chemie [Ullmann's Encyclopedia of Industrial Chemistry], 4th Edition (1981), Vol. 6, pages 376 ff.
Before the wastewater can be introduced into conventional purification plants, rivers or streams, or other receiving bodies, its content of organic impurities must be markedly decreased in order to comply with the strict legislation with respect to maximum pollutant concentration.
SUMMARY OF THE INVENTION
The object of the Invention is, therefore, to develop a process by means of which the concentration of organic impurities can be considerably decreased in the wastewater, especially to a level which is acceptable for discharge under existing environmental legislation.
According to the invention, this object is achieved by a process which comprises adjusting the wastewater to a pH of 0 to 6, and then extracting the wastewater with monohydric alcohols which contain 8 or more carbon atoms and/or with hydrocarbons which contain more than 6 carbon atoms. If necessary, an organic phase may form on adjusting the pH; if so, it is separated out before extraction.
The novel process is simple to carry out industrially, can easily be adapted to different circumstances, and is distinguished by high economic efficiency and effectiveness. It makes it possible to remove at least 90 percent of the organic impurities in the wastewater.
DETAILED DESCRIPTION OF THE INVENTION
The extraction media used are, according to the invention, higher monohydric alcohols, that is alcohols having 8 or more carbon atoms. Preference is given to alcohols having 8 to 16 carbon atoms; they can be straight or branched chain, saturated or unsaturated. It is not necessary to use pure alcohols; mixtures of isomeric alcohols or of alcohols of different molecular size are also suitable. Those which have proven useful are 2-ethylhexanol, 3,5,5-trimethylhexanol, isooctyl alcohol, nonyl alcohol, decyl alcohol, isodecyl alcohol, and mixtures of isomeric alcohols having 8 to 10 carbon atoms.
In addition to the alcohols, hydrocarbons having more than 6 carbon atoms, in particular those having 6 to 12 carbon atoms, can be used as extraction media. The hydrocarbons, like the alcohols, can be straight or branched chain, saturated or unsaturated. Those which have proven particularly useful are mixtures of different hydrocarbons which are produced as low-boiling fractions in the distillation of mineral oil, in particular light heating oil.
Apart from alcohol mixtures and mixtures of different hydrocarbons, mixtures of alcohols and hydrocarbons can also be used for the extraction of the organic impurities from the wastewater. The mixing ratio can extend over a broad range and is principally restricted by the miscibility of the components. The alcohols and/or hydrocarbons used according to the invention have proven to be excellent extraction media for the organic substances conventionally contained in the wastewater. It is of further importance that they are dissolved in only minor amounts by the water phase.
An important aspect of the novel process is to adjust the generally alkaline wastewater to a pH of 0 to 6, in particular 1 to 3. As a result, virtually complete transfer of the organic components is achieved from the aqueous to the organic phase. Furthermore, by this measure, the solubility of the extraction media in the water is further reduced. It has been found that the solubility of the extraction media is dependent on the pH and is considerably lower in acid than in alkaline media. Therefore, in acid solutions, the extraction media contribute only slightly to the increase in the COD value.
Furthermore, the carboxylic acid salts contained in the wastewater are converted into the corresponding free acids; in accordance with their solubility in water, they form a separate phase which can be separated off even before the extraction step. To adjust the pH, inorganic acids are used, such as hydrochloric acid, sulfuric acid, nitric acid, or phosphoric acid, preferably sulfuric acid.
The extraction of the organic impurities from the wastewater by the process according to the invention is carried out in apparatus conventional for solvent extraction. Those which have proven particularly useful are single or multiple stage extraction batteries, which receive the contaminated wastewater from a plurality of series-connected mixer-separator pairs. Extraction columns having stationary internals, such as packed columns, or having moving internals, such as agitated columns, can likewise be used. The extraction medium and carrier liquid can be conducted in concurrent or, preferably, counter-current flow. Atmospheric pressure and standard temperature conditions are conventionally employed.
The extraction medium can easily be regenerated by distillation and can therefore be used repeatedly. By treatment of the distillation residue, the organic substances contained in the wastewater are isolated.
The novel process is suitable for the treatment of wastewater of the aldolization reaction, independently of the aldolization process employed and the starting materials used. The aldolization can therefore be carried out, e.g., with alkali metal hydroxide, alkali metal carbonate, or amines as catalysts and with aldehydes or ketones as starting materials.
REFERENCES:
patent: 2441602 (1948-05-01), Snow et al.
patent: 3463818 (1969-08-01), Blumenthal
patent: 3839458 (1974-10-01), Prinz
patent: 3920760 (1975-11-01), Heinz
patent: 4083931 (1978-04-01), Lee
patent: 4496770 (1985-01-01), Duembgen et al.
patent: 5026919 (1991-06-01), Dessau
patent: 6139747 (2000-10-01), Rotzheim et al.
Loudon, Organic Chemistry (Second Edition) pp. 28
Denkmann Klaus
Frohning Carl Dieter
Greb Wolfgang
Kalbfell Heinz
Rötzheim Mariola
Bierman, Muserlian and Lucas
Hoechst Aktiengesellschaft
Vargot Mathieu D.
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