Direct method for preparing doped polyaniline, product...

Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – Treating polymer containing material or treating a solid...

Reexamination Certificate

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C528S422000, C528S491000, C528S495000, C528S499000, C528S50200C, C525S191000, C525S221000, C525S230000

Reexamination Certificate

active

06277952

ABSTRACT:

BACKGROUND OF THE INVENTION
This invention relates to conductive polymers, and more particularly to conductive doped polyanilines and compositions containing them
The use of conductive materials as additives for plastics is of considerable interest since increased conductivity is desirable for many applications, including electrostatic painting and dissipation of static charges. For the latter purpose, especially, a very short static decay time, on the order of 0.02 second, is desirable.
Among the conductive additives which have been employed are conductive carbon black and conductive carbon fiber. At high loadings, however, carbon black tends to accumulate at the surface of a plastic part and subsequently slough off the plastic part. Carbon fiber is expensive and can decrease impact resistance of the part.
It is also possible to coat the surfaces of particulate non-conductive fillers such as mica, glass fibers or glass spheres with a conductive metal or compound thereof such as copper, silver or antimony-doped tin oxide. This, however, can cause problems including high cost, insufficient adhesion to the base resin and loss in conductivity as a result of oxidation of the metal coating.
Many of these problems can be alleviated by employing a conductive polymer as the additive. A particularly advantageous conductive polymer is polyaniline, which may be prepared by electrochemical methods or chemically by the oxidation of aniline in the presence of a mineral acid under relatively mild conditions.
These preparation methods typically afford the polyaniline as a partially oxidized and partially reduced material, with the reduced portion comprising —C
6
H
4
NH— structural units and the oxidized portion comprising alternating quinone and phenylene moieties separated by trivalent nitrogen atoms. This partially oxidized and partially reduced polyaniline is known as “emeraldine”. It can be readily converted to the fully oxidized state, known as “pernigraniline”, or to the fully reduced state, known as “leucoemeraldine”. It can also be handled in the protonated state, known as “protonated emeraldine”.
Polyaniline prepared by known methods, including the above-described chemical method, has, however, various problems which detract from its utility as a conductive polymer. As a single example of such a problem, such polyaniline is often contaminated with by-products such as the virulently carcinogenic benzidine.
PCT application 95/06,685 provides a summary of the state of the art of conductive polyaniline production and processing as of 1994, including the doping of polyaniline with such materials as alkylbenzenesulfonic acids. It also discloses a process in which doped polyaniline is combined with a polymer and a “solvent-plasticizer” to form a processable composition. Such a process requires a first step of preparing the polyaniline, a second step of doping it and a third step of combining the doped material with a polymer and a solvent-plasticizer.
It remains of interest, therefore, to prepare a polyaniline which is not contaminated with harmful by-products and which can be prepared in a minimum of steps and then blended with plastic materials to produce a processable conductive material.
SUMMARY OF THE INVENTION
The present invention provides a single-step direct method for preparing doped polyaniline and a method for separating the product from the reaction system I which it was prepared. The product of said method is benzidine-free and has a static decay time which is substantially shorter than that of doped polyaniline prepared by other methods. Said product can be combined in a single blending operation with thermoplastic polymers to afford processable conductive resinous compositions.
In one of its aspects, the invention is a method for preparing an electrically conductive polyaniline which comprises contacting aniline with an oxidizing agent in aqueous solution at a temperature of at most about 10° C. in the presence of at least one organic sulfonic acid. Another aspect of the invention is sulfonic acid-doped polyanilines prepared by this method.
A further aspect is conductive resinous compositions comprising at least one thermoplastic resin and the sulfonic acid-doped polyaniline.
A still further aspect is a method of isolating polyaniline doped with at least one organic sulfonic acid which comprises precipitating said doped polyaniline from aqueous solution by combination with a mixture of water and a C
1-4
water-miscible alkanol and separating the precipitated polyaniline from said solution.
DETAILED DESCRIPTION; PREFERRED EMBODIMENTS
In the method of the invention for polyaniline preparation, aniline is contacted with an oxidizing agent suitable for its conversion to polyaniline. Suitable oxidizing agents are, in general, mild ones and their identities are known in the art. The preferred oxidizing agent, for most purposes, is ammonium peroxydisulfate, (NH
4
)
2
S
2
O
8
.
Also employed is at least one organic sulfonic acid. It may be an aliphatic, aromatic or heterocyclic sulfonic acid; illustrative acids are methanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic acid, 3-carboxy-4-hydroxybenzenesulfonic acid and 8-hydroxyquinoline-5-sulfonic acid. The preferred acids are the alkylbenzenesulfonic acids, most preferably those in which the alkyl groups contain about 4-20 carbon atoms; examples are 2-n-octylbenzenesulfonic acid and 4-n-dodecylbenzenesulfonic acid, the latter often being especially preferred.
Polyaniline preparation is effected by simply bringing the aniline into contact with the oxidizing agent and sulfonic acid at a temperature of at most about 10° C. at which the oxidation reaction takes place, the preferred temperature range being about 0-10° C. An aqueous medium is preferred. When the oxidizing agent is a peroxydisulfate such as ammonium peroxydisulfate, it is used in at least an equimolar amount with respect to the aniline, preferably in a molar ratio in the range of about 1.0-1.2:1. The sulfonic acid is preferably used in the amount of about 5-10 ml per gram of aniline. Most often, the oxidizing agent is added gradually or portionwise to a mixture of water, aniline and sulfonic acid, and the resulting mixture is agitated to facilitate polyaniline formation.
The polyaniline obtained according to the invention is already doped with sulfonic acid and is generally in the form of a suspension in the aqueous medium, said suspension being difficult to filter since the polyaniline particles tend to clog filters of pore size less than about 200 microns or pass through filters with larger pore sizes. According to the polyaniline isolation method of the invention, the suspension is combined with a mixture of water and a C
1-4
water-miscible alkanol such as methanol, ethanol, 1-propanol, 2-propanol or 2-methyl-2-propanol. The preferred alkanol in most instances is 2-propanol, by reason of its particular suitability, availability and low cost.
Combination of the aqueous reaction mixture with the alkanol-water mixture is ordinarily effected under ambient conditions including temperatures in the range of about 20-30° C. Said alkanol-water mixture typically contains an amount up to about 95% by weight water with the balance being alkanol. Upon such combination, the doped polyaniline precipitates as a fine powder which may be easily removed by filtration. After drying, typically in vacuum, it is ready for use.
The entire process of polyaniline preparation and isolation according to the invention is most often completed in a period of 6-8 hours. This is in contrast to the prior art method employing a mineral acid, which may require up to 10 hours for completion.
Sulfonic acid-doped polyanilines prepared and, preferably, isolated by the method of this invention are conductive and may be used in the same way as other conductive polymers. In particular, it may be employed to form a conductive coating on fillers and reinforcing agents of high aspect ratio, such as glass fibers, which may then be incorporated in thermoplastic resins to increase their conductivity.
The dop

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