Chemistry of inorganic compounds – Oxygen or compound thereof – Peroxide
Reexamination Certificate
2000-11-20
2003-02-25
Langel, Wayne A. (Department: 1754)
Chemistry of inorganic compounds
Oxygen or compound thereof
Peroxide
C252S182120, C423S589000, C423S590000
Reexamination Certificate
active
06524547
ABSTRACT:
The present invention relates to a process for production of hydrogen peroxide according to the anthraquinone process, wherein the working solution comprises a certain mixture of anthraquinones and tetrahydro anthraquinones. The invention also concerns a solution of such anthraquinones useful as a working solution at production of hydrogen peroxide.
The most common process for production of hydrogen peroxide is the anthraquinone process. In this process substituted anthraquinones and/or tetrahydro anthraquinones dissolved in a suitable organic solvent mixture, a so called working solution, are hydrogenated to form the corresponding hydroquinones. The hydroquinones are then oxidised back to quinones with oxygen (usually air) with simultaneous formation of hydrogen peroxide, which then can be extracted with water while the quinones are returned with the working solution to the hydrogenation step.
The anthraquinone process is described extensively in the literature, for example in Kirk-Othmer, “Encyclopedia of Chemical Technology”, 4
th
Ed., 1993, Vol.13, pp. 961-995.
The hydrogenation is the most critical step in the anthraquinone process. Particularly, there are problems in minimising the loss of anthraquinones and tetrahydro anthraquinones in undesired side reactions and in reaching a high concentration of hydroquinones in the working solution. It has been found that the composition of the working solution is important to overcome these problems.
WO 95/28350 discloses production of hydrogen peroxide with a working solution mainly consisting of tetrahydro ethyl- and tetrahydro amyl anthraquinones in organic solvents.
WO 98/28225 discloses production of hydrogen peroxide with a working solution consisting of ethyl- and amyl anthraquinones in organic solvents.
It has now been found possible to provide a working solution with high solubility, enabling high concentration of hydroquinones, which working solution also is highly stable against side reactions during the hydrogenation step.
Thus, the present invention concerns a process for production of hydrogen peroxide according to the anthraquinone process comprising the steps of alternate hydrogenation and oxidation of anthraquinones and tetrahydro anthraquinones in a working solution. The working solution to be hydrogenated comprises a mixture of alkyl-substituted anthraquinones and alkyl-substituted tetrahydro anthraquinones dissolved in at least one organic solvent, wherein from 10 to 55 mole %, preferably from 20 to 50 mole 35% of the anthraquinones and the tetrahydro anthraquinones are substituted with one amyl group, and the molar ratio of alkyl-substituted tetrahydro anthraquinones to alkyl-substituted anthraquinones is at least 1:1, preferably from about 2:1 to about 50:1, most preferably from about 3:1 to about 20:1. In some cases it may be appropriate to operate at a molar ratio only up to about 9:1, but it is also possible to use working solutions almost free from alkyl-substituted anthraquinones.
The amyl-substituted anthraquinones and amyl-substituted tetrahydro anthraquinones are suitably mainly made up of 2-tert-amyl- and/or 2-iso-sec-amyl-substituted anthraquinone and tetrahydro anthraquinone, preferably a mixture thereof. Preferably, also from 45 to 90 mole %, most preferably from 55 to 80 mole % of the anthraquinones and tetrahydro anthraquinones are substituted with one or several other alkyl groups, most preferably having totally from 1 to 4 carbon atoms, particularly preferably with one ethyl group. It is most preferred that the alkyl-substituted anthraquinones and tetrahydro anthraquinones are mono-substituted, preferably at the 2-position.
The use of amyl-substituted anthraquinone and amyl-substituted tetrahydro anthraquinone in the working solution means that the corresponding hydroquinones are formed in the hydrogenation step. Since the amyl-substituted hydroquinones have a significantly higher solubility than other alkyl-substituted hydroquinones, it is possible to operate with a high degree of hydrogenation without risking precipitation of hydroquinones in the working solution, even at comparatively low concentrations of amyl-substituted quinones. However, high hydrogenation degrees can only be achieved if the amount of tetrahydro anthraquinones is sufficiently high. Furthermore, losses of active quinones to degradation products increases at low concentrations of tetrahydro anthraquinones. Unwanted precipitation might also occur.
If the amount of amyl-substituted anthraquinone and amyl-substituted tetrahydro anthraquinone is too high, the density of the working solution becomes so high that it will be difficult to extract the hydrogen peroxide with water after the oxidation step. It has been found that the density is lower when the molar fraction of amyl-substituted quinones of total amounts of quinones is kept low. Preferably, the working solution has a density, measured at 20° C., from about 910 to about 980 kg/m
3
, most preferably from about 930 to about 970 kg/m
3
. Furthermore, amyl-substituted anthraquinone is also more complicated to produce compared to ethyl-substituted anthraquinone, which makes it a more expensive ingredient in the working solution.
The molar ratio of alkyl substituted tetrahydro anthraquinones to alkyl substituted anthraquinones in a mature working solution (a working solution used for hydrogen peroxide production during at least six months) is suitably in the same magnitude for the anthraquinones substituted with different alkyl groups. The molar ratio for each alkyl group differ preferably less than with a factor of about 2.5, most preferably less than with a factor of about 1.7.
The alkyl substituted tetrahydro anthraquinones are normally mainly made up of &bgr;-tetrahydro anthraquinones, but also some a-tetrahydro anthraquinones may occur.
Besides the direct or indirect hydrogenation to hydroquinones, many secondary reactions take place. For example, the anthrahydroquinones can react further to tetrahydro anthrahydroquinones, which in the oxidation step is converted to tetrahydro anthraquinones, the content of which thus will increase in the working solution. This means that when the process of the invention is started up, the initial working solution may contain no or only small amounts of tetrahydro anthraquinones, as they will form automatically during the course of operation. As soon as the desirable concentrations of anthraquinones and tetrahydro anthraquinones have been reached, at least a portion of the working solution is then normally treated to dehydrogenate tetrahydro anthraquinones back to anthraquinones.
Direct or indirect formation of unwanted by-products also occur, such as epoxides, octahydro anthraquinones, oxanthrones, anthrones and dianthrones. Some of these compounds, like epoxides can be converted back to anthraquinones, while others, like dianthrones, constitute an irreversible loss of active working solution. It has been found that the formation of undesired by-products can be minimised if the molar ratio of tetrahydro anthraquinones to anthraquinones is maintained within the above specified range.
It is preferred that the working solution to be hydrogenated is substantially free from unsubstituted anthraquinone and tetrahydro anthraquinone, since these compounds have been found to have poor solubility and to easily form octahydro anthrahydroquinone, which cannot readily be oxidised to form hydrogen peroxide. It is particularly preferred that the working solution to be hydrogenated substantially consists of alkyl-substituted, most preferably a mixture of amyl- and ethyl-substituted anthraquinone and tetrahydro anthraquinone in at least one organic solvent, preferably containing less than about 100 kg/m
3
, most preferably less than about 50 kg/m
3
of other compounds, such as epoxides and other degradation products from the anthraquinones and/or the solvents, some of which are not even readily identifiable.
The at least one organic solvent is preferably a mixture of one or more quinone solvents and one or more, most preferably at least two hydroqui
Järnvik Christina
Nyström Mats
Saari Seppo
Thor Hans
Akzo Nobel N.V.
Langel Wayne A.
Serbin David J.
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