Method for isolating enriched source of conducting polymers...

Organic compounds -- part of the class 532-570 series – Organic compounds – Oxygen containing

Reexamination Certificate

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Reexamination Certificate

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06642421

ABSTRACT:

FIELD OF THE INVENTION
The present invention relates to a method for isolating an enriched source of conducting polymer precursors from heterocyclic nitrogen containing hydrocarbon streams.
BACKGROUND OF THE INVENTION
Conducting polymers such as polypyrrole, polyindole, polycarbazole and other polymeric heterocyclic nitrogen containing compounds are valuable commodities (see “Polymers, Electrically Conducting”, by Herbert Naarman, in Ullmann's Encyclopedia of Industrial Chemistry, Vol. A21, VCH Publishers, Inc., 1992, pp. 429-447), the potential uses of which include flexible conductive paths in printed circuit boards, heating films, film keyboards, as electrode materials in rechargeable batteries and as polymer coatings in electrochemical sensor devices. These polymers can be synthesized from suitable monomers or precursors by known processes.
Petroleum streams provide potential sources of such monomers or precursors. However, the concentration of these monomers or precursors is typically very low and they are contaminated with similar boiling point materials, which makes their isolation difficult. These monomers or precursors currently are not valuable as fuel sources, and in fact, act as poisons for catalysts, so their removal from the petroleum streams would provide a dual benefit of removing catalyst poisons from the petroleum stream while facilitating the recovery of compounds having value for use as chemical products.
Petroleum streams contain a wide variety or organo-nitrogen species. Therefore, efforts to remove some of these species, due to their deleterious effects on catalysts used in petroleum processing have made. For example, in U.S. Pat. No. 5,675,043 a process is described which removes nitrites from low-boiling petroleum feed stocks for catalytic conversion processes. Therein model nitrile (RCN) containing hydrocarbon streams were treated at lower temperatures, e.g., 16-149° C., (60-300° F.) using solvents meeting a specific formula. The model feeds did not contain heterocyclic nitrogen compounds such as those characteristic of heavy hydrocarbon feeds, e.g., in feeds having a boiling point of 232-566° C. (450° F. to 1050° F.). Additionally, the reference teaches away from the use of higher process temperatures and the reference notes that selection of solvents cannot be easily determined a priori. Actual petroleum streams are complex mixtures of nitrogen containing compounds and other components. Thus one skilled in the art would not be able to extrapolate from the low-boiling nitrile-containing hydrocarbon stream of the reference to treatment of other, higher-boiling streams containing different organo-nitrogen species.
Other patents describe the removal of basic heterocyclic nitrogen species, such as, quinolines from crude oils or fractions by extraction with carboxylic acids (e.g., U.S. Pat. No. 4,985,139 using carboxylic acids; and U.S. Pat. No. 2,848,375 using boric acid and polyhydroxyorganic compounds). In this case, advantage is taken of the basicity of the target molecule to be removed, by reacting it with an acidic extractant. However, the organonitrogen species remaining in the feed after the treatment with acid are believed to be non-basic heterocyclic nitrogen species. The described method is ineffective for their removal. These “non-basic” heterocyclic nitrogen species, e.g., pyrrole, indole, carbazole and their substituted derivatives fall into this class. However, since they are not believed to be as deleterious to catalyst function as are the basic heterocyclic nitrogens, or to have as negative an impact on petroleum product performance, less effort has been directed at their removal.
It would be desirable to develop processes for selectively isolating or recovering these non-basic nitrogen-containing heterocyclic materials useful as precursors to more valuable products. Applicants invention addresses this need.
SUMMARY OF THE INVENTION
An embodiment of the present invention provides for contacting a non-basic heterocyclic nitrogen containing hydrocarbon stream having a boiling point of from 232° C. (450° F.) to 566° C. (1050° F.) with an effective amount of a treating agent selected from polyols, polyol ethers having a number average molecular weight of less than 1000 and 1200, respectively, and mixtures thereof, at conditions effective to maintain the reactants in a liquid phase to produce a first stream enriched in non-basic heterocyclic nitrogen containing hydrocarbons and a second treated stream having a decreased non-basic heterocyclic nitrogen content. Optionally, an effective amount of mineral acid may be added in conjunction with the treating agent. Or, optionally the second treated stream is contacted with an effective amount of polyols and polyol ethers having number average molecular weight of less than 1000 and 1200, respectively, and an effective amount of a mineral acid.
The present invention may comprise, consist or consist essentially of the steps recited and may be practiced in the absence of a step or limitation not disclosed as required.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
Electropolymerization reactions require the presence of conducting polymers and appropriate monomers to continue chain growth. For example, to produce polypyrroles, polyindoles or polycarbazoles the corresponding precursor (i.e., monomers) are required; pyrroles, indoles and carbazoles, whether substituted or unsubstituted. By substitution is meant that additional non-interfering organic groups such as alkyl, cycloalkyl, or aryl side-chains may also be found on these monomers. This will typically be the case with monomers derived from petroleum sources.
A preferred embodiment of the present invention provides for a method for, isolating, recovering or concentrating conducting polymer precursors derived from suitable petroleum streams. Thus, the process is useful for producing a concentrate of these precursors.
Certain process streams contain sources of monomers and other subunits or precursors useful for producing conducting polymers. However, such process streams often do not provide these in sufficient concentration or purity, and therefore, have not traditionally been viewed as desirable sources of such precursors. Applicants have discovered a process for recovering and concentrating monomers and other subunits suitable as precursors in the production of conducting polymers from process streams containing them.
These process streams are typically hydrocarbon streams that contain non-basic heterocyclic organo-nitrogen compounds. Optionally, other organonitrogen species may also be present in the stream, but their presence is not required. These non-basic organonitrogen containing compounds are contained in petroleum streams or fractions having a boiling point of from at least 450° F. to 1050° F. (232-566° C.). Preferably, these streams or fractions should be liquid at process conditions.
By “conducting polymers” it is meant organic nitrogen-containing polymers from electropolymerization reactions. The terms “precursors”, “subunits” and the like include monomers, dimers and larger subunits of such organonitrogen containing compounds, e.g., pyrroles, indoles and carbazoles, falling within the above boiling point range of the hydrocarbon streams.
A preferred embodiment of the process provides for contacting a hydrocarbon stream containing such non-basic heterocyclic nitrogen compounds with an effective amount, 10-200% on a volume basis relative to the volume of petroleum feedstock, of a treating agent (solvent) selected from alkylene glycols and polyalkylene glycols, and mixtures thereof. Suitable glycols of the above referenced materials have number average molecular weights of less than 1000, preferably less than 600, and suitable glycol ethers of the above referenced materials have number average molecular weights of less than 1200. Alkylene and polyalkylene glycols include ethylene glycols and polyethylene glycols, respectively, and alkylene and polyalkylene glycol ethers include polyethylene glycol ethers and diethers. More prefer

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