The present invention relates to a method of purifying hydrochloric acid, and more specifically, to a method of producing high-purity hydrochloric acid not containing an organic substance from hydrochloric acid containing the organic substance.
In the process of producing a compound in which a chloro compound is treated, hydrochloric acid is generated as a by-product and the like. This hydrochloric acid usually contains impurities characteristic of the producing process. For example, hydrochloric acid obtained as a by-product in the process of producing allyl chloride from propylene and chlorine gas contains organic impurities having a relatively low boiling point, such as 2-chloropropane (2CP) [bp=36° C.], allyl chloride [bp=23° C.] and isopropyl alcohol (IPA) [bp=82° C.].
Furthermore, hydrochloric acid obtained as a by-product in the process of obtaining isocyanate by the reaction of amine and phosgene contains organic impurities having a relatively high boiling point, such as chlorobenzene [bp=131° C.] and dichlorobenzene [bp=180° C.] which are mainly used as solvents.
In order to effectively utilize the above-described by-product hydrochloric acid as raw materials in other synthetic processes, it is preferable that a very small amount of organic impurities contained in the by-product hydrochloric acid is removed to the maximum extent possible. For example, Japanese Patent Laying-Open No. 2003-112907 (Patent Document 1) discloses that an organic substance in hydrogen chloride is removed by activated carbon adsorption.
However, it is difficult by the activated carbon adsorption to obtain high-purity hydrochloric acid by removing organic impurities having a relatively low boiling point from hydrochloric acid containing the organic impurities such as hydrochloric acid produced as a by-product in the process of producing allyl chloride.
An object of the present invention is to provide a method of producing high-purity hydrochloric acid substantially not containing an organic substance having a relatively low boiling point, specifically, −25° C. to 120° C., under atmospheric pressure, from hydrochloric acid containing the organic substance.
The present invention provides a method of purifying hydrochloric acid by removing an organic substance having a boiling point of −25° C. to 120° C. under atmospheric pressure from an organic substance-containing hydrochloric acid that contains the organic substance and has a hydrogen chloride concentration higher than an azeotropic hydrogen chloride concentration under atmospheric pressure. The method includes the step of subjecting the organic substance-containing hydrochloric acid to distillation using a distillation tower at an operation pressure set such that an azeotropic hydrogen chloride concentration under the operation pressure is higher than the hydrogen chloride concentration of the organic substance-containing hydrochloric acid, to distill out the organic substance from a top of the distillation tower.
It is preferable that the method of purifying hydrochloric acid according to the present invention includes the steps of: continuously introducing the organic substance-containing hydrochloric acid into the distillation tower; and subjecting the organic substance-containing hydrochloric acid to distillation using the distillation tower at the operation pressure set such that the azeotropic hydrogen chloride concentration under the operation pressure is higher than the hydrogen chloride concentration of the organic substance-containing hydrochloric acid, to distill out the organic substance from the top of the distillation tower and continuously collect hydrochloric acid substantially not containing the organic substance from a bottom of the distillation tower. Furthermore, the operation pressure is preferably in a range of 1 kPa to 90 kPa.
During the distillation of the organic substance-containing hydrochloric acid, it is preferable that the organic substance is distilled out from the top of the distillation tower while reflux is performed for condensing distillate gas from the top of the distillation tower and returning a part of an obtained condensate liquid to the top of the distillation tower.
The organic substance removed by the method of purifying hydrochloric acid according to the present invention is an organic substance having a boiling point of −25° C. to 120° C. under atmospheric pressure and suitable examples thereof include isopropyl alcohol, 2-chloropropane, allyl chloride, and the like.
According to the present invention, organic impurities can be effectively removed from hydrochloric acid containing the organic impurities having a boiling point of −25° C. to 120° C. under atmospheric pressure, and particularly, from hydrochloric acid containing the organic impurities and having a hydrogen chloride concentration higher than an azeotropic hydrogen chloride concentration under atmospheric pressure. Consequently, high-purity hydrochloric acid can be obtained.
Furthermore, the purifying method according to the present invention allows complete or almost complete elimination of the loss of hydrogen chloride, due to purification process, that is contained in the organic substance-containing hydrochloric acid subjected to purification. Accordingly, purified hydrochloric acid containing the total or almost total amount of hydrogen chloride contained in the organic substance-containing hydrochloric acid subjected to purification can be obtained.
The present invention relates to a method of purifying hydrochloric acid by removing an organic substance having a boiling point of −25° C. to 120° C. under atmospheric pressure from an organic substance-containing hydrochloric acid that contains the organic substance and has a hydrogen chloride concentration higher than an azeotropic hydrogen chloride concentration under atmospheric pressure.
Hydrochloric acid containing the organic substance subjected to the purifying method according to the present invention is the organic substance-containing hydrochloric acid that contains the organic substance having a boiling point of −25° C. to 120° C. under atmospheric pressure and has a hydrogen chloride concentration higher than an azeotropic hydrogen chloride concentration under atmospheric pressure. The organic substance having a boiling point of −25° C. to 120° C. under atmospheric pressure, that can be removed according to the present invention, may include various types of organic substances including, for example, isopropyl alcohol (IPA) [bp (the boiling point at 1 atm; the same shall apply hereinafter)=82° C.], 2-chloropropane (2-CP) [bp=36° C.], allyl chloride [bp=23° C.], carbon tetrachloride [bp=77° C.], dichloromethane [bp=40° C.], chloromethane [bp=−24° C.], dichloroethane [bp=57° C.], a vinyl chloride monomer [bp=−14° C.], and the like. Particularly, the present invention allows effective removal of isopropyl alcohol, 2-chloropropane, allyl chloride, and the like in hydrochloric acid. The number of types of the organic substances contained in the organic substance-containing hydrochloric acid may be only one or two or more. The concentration of the organic substance contained in the organic substance-containing hydrochloric acid is not particularly limited, but is usually approximately 1 to 10000 mass ppm in the organic substance-containing hydrochloric acid, and preferably, approximately 10 to 1000 mass ppm.
The organic substance-containing hydrochloric acid subjected to the purification method according to the present invention has a hydrogen chloride concentration mass of hydrogen chloride)/(the total mass of hydrogen chloride and water contained in the organic substance-containing hydrochloric acid)×100%] higher than the azeotropic hydrogen chloride concentration of hydrochloric acid under atmospheric pressure (usually, approximately 80 kPa to 120 kPa (absolute pressure). The “azeotropic hydrogen chloride concentration under atmospheric pressure” means the concentration of hydrogen chloride on the mass basis in the azeotropic composition of hydrochloric acid under atmospheric pressure. The relationship between the pressure and the azeotropic hydrogen chloride concentration of hydrochloric acid is described, for example, in “Soda Handbook” (published by Japan Soda Industry Association in 1998) and the like. The specific numerical value of the “azeotropic hydrogen chloride concentration under atmospheric pressure” can be referred to the document.
The hydrogen chloride concentration of the organic substance-containing hydrochloric acid subjected to the purification method according to the present invention is not limited as long as it exceeds the azeotropic hydrogen chloride concentration of hydrochloric acid under atmospheric pressure as described above, but preferably, 20 percent by mass or more and 24 percent by mass or less, and more preferably, 21 percent by mass or more and 23.5 percent by mass or less. As described below, in the purification method according to the present invention, the organic substance-containing hydrochloric acid is subjected to distillation while adjusting the operation pressure such that the azeotropic hydrogen chloride concentration under the operation pressure is higher than the hydrogen chloride concentration of the organic substance-containing hydrochloric acid. When the hydrogen chloride concentration of the organic substance-containing hydrochloric acid exceeds 24 percent by mass, the operation pressure satisfying the above-described conditions cannot be achieved (see
In the present invention, referring to
Organic substance-containing hydrochloric acid 1 introduced into distillation tower 101 is subjected to distillation. The distillation causes the organic substance to be distilled and removed out of the top of distillation tower 101. A purified hydrochloric acid 3 substantially not containing any organic substance is collected from the bottom of distillation tower 101. The organic substance is collected from the top of the tower as a mixture 2 of the organic substance and water (see
In the present invention, the operation pressure in the above-described distillation is set such that the azeotropic hydrogen chloride concentration under the operation pressure is higher than the hydrogen chloride concentration of the organic substance-containing hydrochloric acid subjected to distillation. The value of the operation pressure satisfying such a condition is determined based on the hydrogen chloride concentration of the organic substance-containing hydrochloric acid and the relationship between the pressure and the azeotropic hydrogen chloride concentration of hydrochloric acid shown in
It is preferable that the operation pressure for distillation is selected from the range of 1 kPa to 90 kPa (absolute pressure). The pressure reduced below 1 kPa may be difficult to be achieved in a manufacturing plant and the like. The present invention employs the organic substance-containing hydrochloric acid subjected to distillation that has a hydrogen chloride concentration higher than the azeotropic hydrogen chloride concentration under atmospheric pressure. Accordingly, the operation pressure should inevitably be lower than atmospheric pressure in order to set the azeotropic hydrogen chloride concentration under the operation pressure to be higher than the hydrogen chloride concentration of the organic substance-containing hydrochloric acid subjected to distillation. When the hydrogen chloride concentration of the organic substance-containing hydrochloric acid is extremely close to the azeotropic hydrogen chloride concentration (20.2 percent by mass) at 101.3 kPa (=1 atm), the operation pressure is at least set below 101.3 kPa. This allows removal of the organic substance while preventing distillation of hydrogen chloride out of the top of the tower. In this case, however, it is preferable to set the operation pressure at 80 kPa or lower in order to more effectively prevent distillation of hydrogen chloride out of the top of the tower. In general, the greater the difference is between the operation pressure and the pressure at which the hydrogen chloride concentration of the organic substance-containing hydrochloric acid subjected to distillation is equal to the azeotropic hydrogen chloride concentration, the more effectively distillation of hydrogen chloride out of the top of the tower can be prevented.
The operation temperature for distillation (the temperature at the bottom of the distillation tower) depends on the operation pressure and the like, but is usually approximately 18° C. to 106° C.
The type of the distillation tower is not particularly limited, and may be a commonly used distillation tower such as a packed tower or a tray tower, in which case a packed tower is preferable since it has a simplified structure. Examples of a packing agent packed into the packed tower may include, for example, a conventional agent such as Raschig ring, Paul ring, or Tellerette (registered trademark). In order to more efficiently suppress or prevent distillation of hydrogen chloride out of the top of the tower, it is preferable, as shown in
Distillation of the organic substance-containing hydrochloric acid can be performed either in a continuous manner or in a batch-wise manner, but preferably performed in a continuous manner. In the case where distillation is performed in a batch-wise manner and there is only a slight difference between the operation pressure and the pressure at which the hydrogen chloride concentration of the organic substance-containing hydrochloric acid subjected to distillation is equal to the azeotropic hydrogen chloride concentration, the operation pressure may need to be shifted to be further reduced in accordance with development of distillation in order to prevent distillation of hydrogen chloride out of the top of the tower. When distillation is performed in a continuous manner, the organic substance-containing hydrochloric acid is continuously introduced into the distillation tower while continuously collecting the mixture of the organic substance and water from the top of the tower and also continuously collecting the purified hydrochloric acid from the bottom of the tower. Consequently, the hydrogen chloride concentration of the organic substance-containing hydrochloric acid within the distillation tower can be kept stationary. This eliminates the need to adjust the operation pressure during distillation.
Purified hydrochloric acid obtained by the method according to the present invention is high-purity hydrochloric acid substantially not containing any organic substance (for example, approximately 0.1 mass ppm or lower). Furthermore, according to the method of the present invention, hydrogen chloride is hardly distilled out of from the top of the tower during distillation. Accordingly, the resultant purified hydrochloric acid is to contain a total or an approximately total amount of hydrogen chloride contained in the organic substance-containing hydrochloric acid introduced into the distillation tower. Therefore, the loss of hydrogen chloride caused by the purification process can be completely or nearly completely suppressed.
Since the purified hydrochloric acid obtained by the method according to the present invention is high-purity hydrochloric acid substantially not containing an organic substance, the purified hydrochloric acid can be suitably used as a raw material in the compound synthesizing process such as a hydrochloric acid oxidation process and also used as hydrochloric acid for food additives. Furthermore, in the case where the purified hydrochloric acid is used as hydrochloric acid for neutralization of alkaline waste water, the produced neutralized water can be released as waste water since it does not substantially contain any organic substance.
Although the present invention will be hereinafter described in more detail with reference to an Example, the present invention is not limited thereto.
As shown in
It should be understood that the embodiments and examples disclosed herein are illustrative and non-restrictive in every respect. The scope of the present invention is defined by the claims, rather than the description above, and is intended to include any modifications within the scope and meaning equivalent to the claims.
Number | Date | Country | Kind |
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2008-308724 | Dec 2008 | JP | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/JP2009/069766 | 11/24/2009 | WO | 00 | 6/1/2011 |