Process for production of carbonaceous chars having...

Catalyst – solid sorbent – or support therefor: product or process – Solid sorbent – Free carbon containing

Reexamination Certificate

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C204S157470

Reexamination Certificate

active

06534442

ABSTRACT:

FIELD OF THE INVENTION
The present invention relates to a process for the production of a catalytically active carbonaceous char, and in particular to a catalytically active char produced at low temperatures and activated at high temperature.
BACKGROUND OF THE INVENTION
The use of carbonaceous chars as catalysts in chemical reactions is well known. Applications that use catalytic chars to improve reaction rate include, but are not limited to NO
X
reduction, SO
X
oxidation, chloramine removal, glyphosate production, peroxide destruction, and metalloid and non-metalloid hydride oxidation. In many of these applications the rate of reaction can be affected by the degree of catalytic activity of the char.
The known techniques for increasing the catalytic activity of carbonaceous chars can generally be categorized into three approaches. One approach involves treating a high-temperature carbonaceous char after the completion of the thermal processing used to produce the char. High-temperature carbonaceous chars, as referred to in this disclosure, are those produced at temperatures equal to or greater than 700° C. Examples of such high-temperature chars are activated carbon and charcoal. Chars produced at temperatures below 700° C. are referred to as low-temperature chars. In one example of this prior art, a high-temperature char is impregnated with metal ions to improve the catalytic performance of the char in NO
X
removal applications. It is also known that exposing activated carbon to ammonia in an oxidizing environment increases the catalytic activity of the carbon. Similarly, oxidizing an activated carbon, followed by inert heat treatment to drive off the oxygen-containing groups from the surface of the carbon enhances the catalytic performance in SO
2
/SO
3
conversion. It is known furthermore that the catalytic oxidative activity of an activated carbon is improved by first oxidizing the carbon and then heating the oxidized carbon in the presence of nitrogen-containing compounds such as urea or melamine.
A second approach for increasing the catalytic activity of carbonaceous chars begins with a carbonaceous feedstock which is inherently suitable to yield a high degree of catalytic activity in the final carbonaceous chars. Such a feedstock is simply thermally processed to produce the catalytically active chars. Those skilled in the art are aware that the catalytic activity is affected by the nitrogen content of the feedstock. For example, pure nitrogen-rich compounds such as hexamethylenetetramine, polyacrylonitrile, or gelatin will, when carbonized and activated, produce carbonaceous chars with catalytic activity. Additionally, admixing ammonium salts with inherently nitrogen-poor feedstock, followed by carbonizing and activating, is known to improve NO
X
reduction performance of the char beyond what is achieved without the addition of the ammonium salts. Similar improvements in the decomposition of hydrogen peroxide are realized with a char made by admixing a nitrogen-containing compound such as urea with a nitrogen-poor feedstock such as sucrose prior to carbonizing and activating.
A more recent approach for increasing the catalytic activity of carbonaceous chars involves modifications to the thermal processes used to produce the chars. Catalytic activity has been significantly enhanced by carbonization and oxidation of a nitrogen-poor bituminous material followed by impregnation of the resultant low-temperature char with a nitrogen-containing compound prior to or during exposure of the char to temperatures of 700° C. or greater. The resultant high-temperature carbonaceous char may then be activated to the desired degree by any known technique. In this approach, the benefit of extensive oxidation of the carbonized product prior to impregnation with a nitrogen-containing compound is taught.
The relative catalytic activity of carbonaceous chars has been shown to be accurately and conveniently classified by determining the ability of the chars to catalyze the decomposition of hydrogen peroxide in an aqueous solution, as set forth in U.S. Pat. No. 5,470,748 (1995). The decomposition reaction is exothermic and, therefore, causes an increase in the temperature of the solution. Under a defined set of conditions, the elapsed time to achieve 75% of the temperature change resulting from complete decomposition of the hydrogen peroxide, or “t-¾ time”, depends solely on the ability of a char to catalyze the hydrogen peroxide decomposition reaction. For instance, two chars may exhibit similar physical adsorptive capacity measured in terms of the Iodine Number, for example, yet have significantly different t-¾ times. Iodine Number is described in Test Method TM-4 of Calgon Carbon Corporation, Pittsburgh, Pa., and is an indication of the available surface area of the char for adsorption. Chars having low t-¾ values are known to be useful for NO
X
reduction,_SO
2
oxidation, chloramine removal, glyphosate production, peroxide destruction, and metalloid and non-metalloid hydride oxidation.
Thus, it is known that the peroxide decomposition ability of a char made from a nitrogen-poor carbonaceous feedstock can be improved by combining said feedstock with nitrogen-containing compounds prior to thermal processing. It is also known that carbonizing a nitrogen-poor carbonaceous feedstock under an oxidizing environment, followed by impregnating the oxidized carbonized product with a nitrogen-containing compound, will enhance peroxide decomposition ability of the final activated char. However, it is not taught by, nor can it be inferred from, the prior art that combining a nitrogen-rich compound with a nitrogen-poor carbonaceous feedstock, and then carbonizing the mixture in an oxidizing environment, will enhance the hydrogen peroxide decomposition ability of the final activated char beyond that achieved without said oxidizing environment or, conversely, without said addition of nitrogen-containing compound. The principal disadvantage expected in such a process would be the oxidation and loss of the nitrogen-containing compound prior to high-temperature treatment, and the consequent need for large amounts of these materials during processing to confer the requisite catalytic activity to the final product. If a unique and significant t-¾ benefit could be obtained from such a process using relatively small amounts of the nitrogen-containing compound, the process would have significant cost and performance advantages over the prior art. For example, those prior art methods which rely on treatment with added metals to produce catalytic activity impose a cost burden due to special handling and disposal procedures associated with the metals. Prior art methods which rely on the use of pure nitrogen-rich compounds as feedstocks also bear a cost burden due to the high cost of the feedstock and to the hazard created by large amounts of cyanide and other toxic materials which are invariably produced during thermal processing. Furthermore, prior art processes that use high temperature chars, such as activated carbons and charcoals, as feedstocks are inherently more costly because of the additional process steps needed to confer catalytic activity to the final product.
Accordingly, it is an object of the present invention to provide an improved low-cost process for the production of carbonaceous chars having improved catalytic activity that are made from nitrogen-poor feedstocks without the use of added metals or post-treatments of high-temperature chars. It is a further object of the present invention to provide these improved cost and performance advantages through relatively minor and low-cost modifications of both the feedstock and the processing conditions typically used to make high temperature chars.
SUMMARY OF THE INVENTION
The present invention comprises a method for the production of carbonaceous chars having significant catalytic activity from nitrogen-poor feedstocks that are treated at low-temperatures.
1
The method of the present invention includes the steps of treating a

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