Conductive sealant compositions

Information

  • Patent Grant
  • 9484123
  • Patent Number
    9,484,123
  • Date Filed
    Monday, September 10, 2012
    11 years ago
  • Date Issued
    Tuesday, November 1, 2016
    7 years ago
Abstract
Embodiments of the present disclosure are directed to sealant compositions including a base composition with at least one sulfur-containing polymer, a curing agent composition, and an electrically conductive filler including carbon nanotubes and stainless steel fibers. The electrically conductive filler can be in either or both of the base composition and the curing agent composition. The sealant compositions are substantially Ni-free and exhibit unexpectedly superior EMI/RFI shielding effectiveness.
Description
TECHNICAL FIELD

The present disclosure relates to sealant compositions exhibiting enhanced EMI/RFI shielding effectiveness.


BACKGROUND

During flight, aircraft face a number of environmental occurrences that can cause dangerous conditions or even physical damage. For example, lightning strikes and electromagnetic interference (EMI) are fairly common environmental occurrences that may lead to dangerous conditions during aircraft flight. Lightning strikes may cause physical damage to the aircraft by puncturing holes through parts of the aircraft, or may cause a dangerous surge current which may contact the fuel reservoir and result in an explosion. EMI may cause excessive energy levels in the wiring and probes of the aircraft's fuel system. Additionally, the electromagnetic noise caused by EMI may result in serious operational difficulties in the electronic components of the aircraft. Given the potential for severe damage or electrical interference caused by these environmental occurrences, means for preventing or mitigating the adverse effects of lightning strikes and EMI are important in aircraft design and manufacture.


SUMMARY

In embodiments of the present invention, a sealant composition includes a base composition having a sulfur-containing polymer, a curing agent composition having a curing agent, and an electrically conductive filler in at least one of the base composition or the curing agent composition. The electrically conductive filler includes carbon nanotubes and stainless steel fibers.


In some embodiments, the sealant composition is substantially nickel free.


The stainless steel fibers may have an average particle dimension larger than an average particle dimension of the carbon nanotubes, or the carbon nanotubes may have an average particle dimension larger than an average particle dimension of the stainless steel fibers. In some embodiments, for example, the carbon nanotubes may have an average length dimension of about 5 μm to about 30 μm, and an average diameter dimension of about 10 nm to about 30 nm, and the stainless steel fibers may have an average first dimension of about 8 μm to about 22 μm, and an average second dimension of about 330 μm to about 1 mm. Also, the volume ratio of the carbon nanotubes to the stainless steel fibers may be about 1:1 to 1:50.


In some embodiments, the sealant compositions further include at least one of an adhesion promoter, a corrosion inhibitor or a plasticizer in at least one of the base composition or the curing agent composition.


In some embodiments, the sulfur-containing polymer is a polysulfide or a polythioether.


According to some embodiments, a sealant composition includes a substantially nickel-free base composition including a sulfur-containing polymer, a substantially nickel-free curing agent composition including a curing agent, and a substantially nickel-free electrically conductive filler in at least one of the base composition or the curing agent composition. The electrically conductive filler includes carbon nanotubes and stainless steel fibers. The stainless steel fibers may have an average particle dimension larger than an average particle dimension of the carbon nanotubes, or the carbon nanotubes have an average particle dimension larger than an average particle dimension of the stainless steel fibers. In some embodiments, for example, the carbon nanotubes have an average length dimension of about 5 μm to about 30 μm, and an average diameter dimension of about 10 nm to about 30 nm, and the stainless steel fibers have an average first dimension of about 8 μm to about 22 μm, and an average second dimension of about 330 μm to about 1 mm. Also, the volume ratio of the carbon nanotubes to the stainless steel fibers may be about 1:5 to 1:50.


The sealant compositions are substantially Ni-free and exhibit unexpectedly superior EMI/RFI shielding effectiveness.







DETAILED DESCRIPTION

In certain embodiments of the present disclosure, a sealant composition comprises at least one sulfur-containing polymer, and an electrically conductive filler comprising carbon nanotubes and stainless steel fibers. The term “sealant,” “sealing,” or “seal” as used herein refers to compositions that have the ability to resist atmospheric conditions such as moisture and temperature and at least partially block the transmission of materials such as water, fuel, and other liquids and gasses. Sealants often have adhesive properties, but are not simply adhesives that do not have the blocking properties of a sealant.


Sealant compositions of the present disclosure can be prepared by blending an electrically conductive base composition, and a curing agent composition. A base composition and a curing agent composition can be prepared separately, and then blended to form a sealant composition. A conductive base composition can comprise, for example, at least one sulfur-containing polymer, at least one plasticizer, at least one adhesion promoter, at least one corrosion inhibitor, at least one electrically non-conductive filler, and an electrically conductive filler comprising carbon nanotubes and stainless steel fibers. However, it is understood that the base compositions need not contain each of these components. For example, many of these components are optional, for example, the plasticizer, adhesion promoter, corrosion inhibitor, electrically non-conductive filler, and electrically conductive filler. Accordingly, the base composition, in some embodiments, may contain only the polymer (which may be either or both a polysulfide and/or a polythioether), and a solvent. However, as discussed below, at least one of the base composition and/or curing agent composition includes a conductive filler comprising carbon nanotubes and stainless steel fibers.


A curing agent composition can comprise, for example, at least one curing agent, at least one plasticizer, at least one electrically non-conductive filler, at least one electrically conductive filler, and at least one cure accelerator. However, like the base composition, the curing agent composition need not contain each of these components. Indeed, many of these components are optional, for example, the plasticizer, electrically non-conductive filler, electrically conductive filler, and cure accelerator. Accordingly, the curing agent composition, in some embodiments, may contain only the curing agent. However, as discussed below, at least one of the base composition and/or curing agent composition includes a conductive filler comprising carbon nanotubes and stainless steel fibers.


In certain embodiments, 5 to 20 parts by weight of a curing agent composition are blended with 100 parts by weight of a base composition, and in certain embodiments, 8 to 16 parts by weight of curing agent composition are blended with 100 parts by weight of a base composition to form an electrically conductive sealant composition.


In certain embodiments, two-component curable compositions are preferred over one-component curable compositions because the two-component compositions provide the best rheology for application and exhibit desirable physical and chemical properties in the resultant cured composition. As used herein, the two components are referred to as the base composition, and the curing agent composition. In certain embodiments, the base composition can comprise polysulfide polymers, polythioether polymers, oxidizing agents, additives, fillers, plasticizers, organic solvents, adhesion promoters, corrosion inhibitors, and combinations thereof. However, it is understood that the base compositions need not contain each of these components. For example, many of these components are optional, for example, the oxidizing agents, additives, fillers, plasticizers, adhesion promoters, and corrosion inhibitors. Accordingly, the base composition, in some embodiments, may contain only the polymer (which may be either or both a polysulfide and/or a polythioether), and a solvent. However, as discussed below, at least one of the base composition and/or curing agent composition includes a conductive filler comprising carbon nanotubes and stainless steel fibers.


In certain embodiments, the curing agent composition can comprise curing agents, cure accelerators, cure retardants, plasticizers, additives, fillers, and combinations thereof. However, like the base composition, the curing agent composition need not contain each of these components. Indeed, many of these components are optional, for example, the cure accelerators, cure retardants, plasticizers, additives, and fillers. Accordingly, in some embodiments, the curing agent composition may contain only the curing agent. However, as discussed below, at least one of the base composition and/or curing agent composition includes a conductive filler comprising carbon nanotubes and stainless steel fibers.


At least one of the base composition and the curing composition includes a conductive filler comprising carbon nanotubes and stainless steel fibers. The conductive filler may further include any additional conductive filler conventionally used in sealant compositions. However, in some embodiments, the optional additional conductive filler is substantially Ni-free in order to reduce toxicity and adverse environmental concerns. In some embodiments, for example, the conductive filler includes graphite in addition to the carbon nanotubes and stainless steel fibers. As used herein, the term “substantially” is used as a term of approximation, and not as a term of degree. Additionally, the term “substantially nickel-free” is used as a term of approximation to denote that the amount of nickel in the additional conductive filler or sealant composition is negligible, such that if nickel is present in the additional conductive filler or sealant composition at all, it is as an incidental impurity.


In certain embodiments, sulfur-containing polymers useful in the practice of the present disclosure include polysulfide polymers that contain multiple sulfide groups, i.e., —S—, in the polymer backbone and/or in the terminal or pendent positions on the polymer chain. Such polymers are described in U.S. Pat. No. 2,466,963 wherein the disclosed polymers have multiple —S—S-linkages in the polymer backbone, the entire content of which is incorporated herein by reference. Other useful polysulfide polymers are those in which the polysulfide linkage is replaced with a polythioether linkage, i.e., —[—CH2—CH2—S—CH2—CH2—]n— where n can be an integer ranging from 8 to 200 as described in U.S. Pat. No. 4,366,307, the entire content of which is incorporated herein by reference. In some embodiments, for example, the polythioether polymers may be those described in U.S. Pat. No. 6,172,179, the entire content of which is incorporated herein by reference. For example, the polythioether polymer may be the polythioether prepared in Example 1 of U.S. Pat. No. 6,172,179. The polysulfide polymers can be terminated with non-reactive groups such as alkyl, although in certain embodiments, the polysulfide polymers contain reactive groups in the terminal or pendent positions. Typical reactive groups are thiol, hydroxyl, amino, and vinyl. Such polysulfide polymers are described in the aforementioned U.S. Pat. No. 2,466,963, U.S. Pat. No. 4,366,307, and U.S. Pat. No. 6,372,849, the entire content of each of which is incorporated herein by reference. Such polysulfide polymers can be cured with curing agents that are reactive with the reactive groups of the polysulfide polymer.


Sulfur-containing polymers of the present disclosure can have number average molecular weights ranging from 500 to 8,000 grams per mole, and in certain embodiments, from 1,000 to 5,000 grams per mole, as determined by gel permeation chromatography using a polystyrene standard. For sulfur-containing polymers that contain reactive functional groups, the sulfur-containing polymers can have average functionalities ranging from 2.05 to 3.0, and in certain embodiments ranging from 2.1 to 2.6. A specific average functionality can be achieved by suitable selection of reactive components. Nonlimiting examples of sulfur-containing polymers include those available from PRC-DeSoto International, Inc. under the trademark PERMAPOL, specifically, PERMAPOL P-3.1 or PERMAPOL P-3, and from Akros Chemicals, such as THIOPLAST G4.


A sulfur-containing polymer can be present in the base composition in an amount ranging from about 10% to about 80% by weight of the total weight of the base composition, and in certain embodiments can range from about 10% to about 40% by weight, and in other embodiments can range from about 20% to about 30% by weight. In certain embodiments, the sulfur-containing polymer comprises a combination of a polysulfide polymer and a polythioether polymer, and the amounts of polysulfide polymer and polythioether polymer can be similar. For example, in some embodiments, the amount of polysulfide polymer and the amount of polythioether polymer in a base composition can each range from about 10% by weight to about 15% by weight of the total weight of the base composition.


The sealant compositions of the present disclosure comprise at least one curing agent for curing the at least one sulfur-containing polymer. The term “curing agent” refers to any material that can be added to a sulfur-containing polymer to accelerate the curing or gelling of the sulfur-containing polymer. Curing agents are also known as accelerators, catalysts or cure pastes. In certain embodiments, the curing agent is reactive at a temperature ranging from 10° C. to 80° C. The term “reactive” means capable of chemical reaction and includes any level of reaction from partial to complete reaction of a reactant. In certain embodiments, a curing agent is reactive when it provides for cross-linking or gelling of a sulfur-containing polymer.


In certain embodiments, the sealant compositions comprise at least one curing agent that contains oxidizing agents capable of oxidizing terminal mercaptan groups of the sulfur-containing polymer to form disulfide bonds. Useful oxidizing agents include, for example, lead dioxide, manganese dioxide, calcium dioxide, sodium perborate monohydrate, calcium peroxide, zinc peroxide, and dichromate. The curing agent may also be an epoxy resin, or the curing agent may include a mixture of another oxidizing agent and an epoxy resin. The amount of curing agent in a curing agent composition can range from about 25% by weight to about 75% by weight of the total weight of the curing agent composition. Additives such as sodium stearate can also be included to improve the stability of the accelerator. For example, a curing agent composition can comprise an amount of cure accelerator ranging from about 0.1% to about 1.5% by weight based on the total weight of the curing agent composition.


In certain embodiments, sealant compositions of the present disclosure can comprise at least one curing agent containing at least one reactive functional group that is reactive with functional groups attached to the sulfur-containing polymer. Useful curing agents containing at least one reactive functional group that is reactive with functional groups attached to the sulfur-containing polymer include polythiols, such as polythioethers, for curing vinyl-terminated polymers; polyisocyanates such as isophorone diisocyanate, hexamethylene diisocyanate, and mixtures and isocyanurate derivatives thereof for curing thiol-, hydroxyl- and amino-terminated polymers; and, polyepoxides for curing amine- and thiol-terminated polymers. Nonlimiting examples of polyepoxides include hydantoin diepoxide, Bisphenol-A epoxides, Bisphenol-F epoxides, Novolac-type epoxides, aliphatic polyepoxides, and epoxidized unsaturated resins, and phenolic resins. The term “polyepoxide” refers to a material having a 1,2-epoxy equivalent greater than one and includes monomers, oligomers, and polymers.


The sealant composition can optionally comprise at least one compound to modify the rate of cure. For example, cure accelerants such as dipentamethylene/thiuram/polysulfide mixture can be included in the sealant composition to accelerate the rate of cure, and/or at least one cure retardant such as stearic acid can be added to retard the rate of cure and thereby extend the work life of a sealant composition during application. In certain embodiments, the curing agent composition can comprise an amount of accelerant ranging from about 1% to about 7% by weight, and/or an amount of cure retardant ranging from about 0.1% to about 1% by weight, based on the total weight of the curing agent composition. To control the cure properties of the sealant composition, it can also be useful to include at least one material capable of at least partially removing moisture from the sealant composition such as a molecular sieve powder. In certain embodiments, a curing agent composition can comprise an amount of material capable of at least partially removing moisture ranging from about 0.1% to about t1.5% by weight, based on the total weight of the curing agent composition.


In certain embodiments, sealant compositions of the present disclosure can comprise fillers. As used herein, “filler” refers to a non-reactive component in the composition that provides a desired property, such as, for example, electrical conductivity, density, viscosity, mechanical strength, EMI/RFI shielding effectiveness, and the like.


Examples of electrically non-conductive fillers include materials such as, but not limited to, calcium carbonate, mica, polyamide, fumed silica, molecular sieve powder, microspheres, titanium dioxide, chalks, alkaline blacks, cellulose, zinc sulfide, heavy spar, alkaline earth oxides, alkaline earth hydroxides, and the like. Exemplary fillers may also include high band gap materials such as zinc sulfide and inorganic barium compounds. In certain embodiments, the base composition can comprise an amount of electrically non-conductive filler ranging from about 2% to about 10% by weight, based on the total weight of the base composition, and in certain embodiments, can range from about 3% to about 7% by weight. In certain embodiments, a curing agent composition can comprise an amount of electrically non-conductive filler ranging from less than 6 percent by weight, and in certain embodiments ranging from about 0.5% to about 4% by weight, based on the total weight of the curing agent composition.


According to embodiments of the present disclosure, either or both of the base composition and/or the curing agent composition includes a conductive filler comprising carbon nanotubes and stainless steel fibers. In some embodiments, the sealant composition includes about 80 to about 90% base composition and about 10 to about 20% curing agent composition, and the conductive filler including the carbon nanotubes and stainless steel fibers are included in the base composition. These fillers are used to impart electrical conductivity and EMI/RFI shielding effectiveness to the sealant compositions. The combination of the carbon nanotubes and stainless steel fibers forms an interactive conductive matrix which imparts unexpectedly superior electrical conductivity and EMI shielding effectiveness. In addition, this combination of carbon nanotubes and stainless steel fibers eliminates Ni, which has typically been used in conductive fillers in conventional sealant compositions. Indeed, according to embodiments of the present invention, the conductive filler, as well as the sealant composition, are substantially Ni-free, thereby substantially eliminating the toxicity and environmental downsides attributed to the inclusion of Ni in conventional sealant compositions. As discussed above, as used herein, the term “substantially” is used as a term of approximation, and not as a term of degree. Additionally, as discussed above, the term “substantially nickel-free” is used as a term of approximation to denote that the amount of the nickel in the sealant compositions is negligible, such that if nickel is present at all, it is as an incidental impurity.


The size of the carbon nanotubes and stainless steel fibers can vary as desired to adjust or modify the electrical conductivity and/or EMI shielding effectiveness of the sealant composition. However, in certain embodiments, one of the carbon nanotubes or the stainless steel fibers has an average particle (i.e., nanotube or fiber) dimension that is larger than an average particle (i.e., nanotube or fiber) dimension of the other of the carbon nanotubes or stainless steel fibers. For example, in some embodiments, the carbon nanotubes may have a length dimension ranging from about 5 to about 30 μm, and a diameter dimension ranging from about 10 to about 30 nm. The stainless steel fibers may have dimensions of about 8 μm×about 330 μm to about 22 μm×about 1 mm. Also, a volume ratio of the carbon nanotubes to the stainless steel fibers may range from about 1:5 to about 1:50. In one embodiment, for example, the volume ratio of the carbon nanotubes to the stainless steel fibers is about 1:5.


The sealant compositions may also optionally include one or more corrosion inhibitors Nonlimiting examples of suitable corrosion inhibitors include strontium chromate, calcium chromate, magnesium chromate, and combinations thereof. U.S. Pat. No. 5,284,888 and U.S. Pat. No. 5,270,364, the entire contents of which are incorporated herein by reference, disclose the use of aromatic triazoles to inhibit corrosion of aluminum and steel surfaces. In certain embodiments, a sacrificial oxygen scavenger such as Zn can be used as a corrosion inhibitor. In certain embodiments, the corrosion inhibitor can comprise less than 10% by weight of the total weight of the sealant composition. In certain embodiments, the corrosion inhibitor can comprise an amount ranging from about 2% by weight to about 8% by weight of the total weight of the sealant composition.


In certain embodiments, the sealant compositions may optionally further comprise one or more plasticizers, nonlimiting examples of which include phthalate esters, chlorinated paraffins, hydrogenated terphenyls, partially hydrogenated terphenyls, and the like. The plasticizer may be included in either or both of the base composition and/or the curing agent composition. In some embodiments, the plasticizer is included in the base composition in an amount ranging from about 0.1% to about 5% by weight based on the total weight of the base composition, and in certain embodiments, can range from about 0.5% to about 3% by weight. In some embodiments, the plasticizer is included in the curing agent composition in an amount ranging from about 20% to about 60% by weight of the total weight of the curing agent composition, and in certain embodiments, can range from about 30% to about 40% by weight.


In certain embodiments, the sealant compositions may optionally further comprise an organic solvent, such as a ketone or an alcohol, for example methyl ethyl ketone, and isopropyl alcohol, or a combination thereof.


In certain embodiments, the sealant compositions may optionally further comprise one or more adhesion promoters, nonlimiting examples of which include phenolic resins, silane adhesion promoters, and combinations thereof. Adhesion promoters help facilitate adhesion of the polymeric components of the sealant composition to a substrate, as well as to the electrically non-conductive and electrically conductive fillers in the sealant composition. The adhesion promoter may be included in either or both of the base composition and/or the curing agent composition. In certain embodiments, the adhesion promoter is included in the base composition in an amount ranging from about 0.10% to about 5.0% by weight (for phenolic adhesion promoters), from about 0.05% to about 1.0% by weight (for mercapto-silane adhesion promoters), or from about 0.05% to about 1.0% by weight (for epoxy-silane adhesion promoters). The total amount of adhesion promoter in the base composition can range from about 0.5% to 7% by weight, based on the total weight of the base composition.


In certain embodiments, the base composition can be prepared by batch mixing at least one sulfur-containing polymer, additives, and/or fillers in a double planetary mixer under vacuum. Other suitable mixing equipment includes a kneader extruder, sigma mixer, or double “A” arm mixer. For example, a base composition can be prepared by mixing at least one sulfur-containing polymer, plasticizer, and phenolic adhesion promoter. After the mixture is thoroughly blended, additional constituents can be separately added and mixed using a high shear grinding blade, such as a Cowless blade, until cut in. Examples of additional constituents that can be added to the base composition include the carbon nanotube/stainless steel conductive filler, corrosion inhibitors, non-conductive fillers, and silane adhesion promoters. The mixture can then be mixed for an additional 15 to 20 minutes under a vacuum of 27 inches of mercury or greater to reduce or remove entrapped air and/or gases. The base composition can then be extruded from the mixer using a high-pressure piston ram.


The curing agent composition can be prepared by batch mixing a curing agent, additives, and fillers. In certain embodiments, 75% of the total plasticizer (such as partially hydrogenated terphenyl) and an accelerant (such as a dipentamethylene/thiuram/polysulfide mixture) are mixed in a single-shaft anchor mixer. Molecular sieve powder is then added and mixed for 2 to 3 minutes. Fifty percent of the total manganese dioxide is then mixed until cut in. Stearic acid, sodium stearate, and the remaining plasticizer are then mixed until cut in followed by the remaining 50% of the manganese dioxide which is mixed until cut in. Fumed silica is then mixed until cut in. If the mixture is too thick a surfactant may be added to increase wetting. The curing agent composition is then mixed for 2 to 3 minutes, passed over a three-roll paint mill to achieve a grind, and returned to the single-shaft anchor mixer and mixed for an additional 5 to 10 minutes. The curing agent composition can then be removed from the mixer with a piston ram and placed into storage containers and aged for at least 5 days prior to combining with a base composition. The base composition and curing agent composition are mixed together to form the sealant composition, which can then be applied to a substrate.


It is noted that, as used in this disclosure, the singular forms “a,” “an,” and, “the” include plural referents unless expressly and unequivocally limited to one referent. Thus, for example, reference to “a filler” includes one or more fillers. Also it is noted that, as used herein, the term “polymer” refers to polymers, oligomers, homopolymers, and copolymers.


For the purposes of this disclosure, unless otherwise indicated, all numbers expressing quantities of ingredients or percentages or proportions of other materials, reaction conditions, and so forth used in the specification and claims are to be understood as being modified in all instances by the term “about.” Accordingly, unless indicated to the contrary, the numerical parameters set forth in the following specification and attached claims are approximations that may vary depending upon the desired properties sought to be obtained by the present disclosure. Embodiments of the present disclosure can be further defined by reference to the following example, which describes in detail the preparation of an exemplary composition of the present disclosure. It will be apparent to those skilled in the art that modifications, both to materials and methods, may be practiced without departing from the scope of the present disclosure.


EXAMPLE

The components of the base composition are indicated in the below table. Specifically, the base composition included 50.7 lbs of a carbon nanotube (CNT) dispersion (i.e., 1% carbon nanotubes dispersed in a polythioether polymer (Permapol P3.1e, available from PRC-DeSoto)), 2.2 lbs conductive graphite, 30.2 lbs stainless steel fibers, and 16.9 lbs solvent.
















Material
Amount (lbs)




















1% CNT in P3.1e
CNT/Polymer
50.7



Graphite
conductive graphite
2.2



Stainless Steel fiber
conductive fibers
30.2



ethyl acetate
solvent
16.9










To the 1% carbon nanotubes dispersed in a polythioether polymer, the graphite is added and mixed in a Hauschild Speed Mixer. The stainless steel fibers and ethyl acetate are then added and dispersed in the Speed Mixer.


The compositions were cured using a manganese or epoxy based curing agent composition to effect oxidative curing. For example, the curing agent composition may include a manganese oxide or epoxy based composition including a plasticizer and/or a cure rate modifier (e.g., a cure accelerant or a cure retardant). One example of a suitable curing agent composition is a composition including about 25% to about 75% manganese dioxide.


The present invention has been described with reference to exemplary embodiments and aspects, but is not limited thereto. Persons skilled in the art will appreciate that other modifications and applications can be made without meaningfully departing from the invention. For example, although the coating compositions are described as being useful for aerospace applications, they may be useful for other applications as well, including in other electronic devices requiring EMI/RFI shielding. Accordingly, the foregoing description should not be read as limited to the precise embodiments and aspects described, but should be read consistent with and as support for the following claims, which are to have their fullest and fairest scope.


Throughout the text and the claims, use of the word “about” in relation to a range of values is intended to modify both the high and low values recited, and reflects the penumbra of variation associated with measurement, significant figures, and interchangeability, all as understood by a person having ordinary skill in the art to which this invention pertains. Additionally, throughout this disclosure and the accompanying claims, it is understood that even those ranges that may not use the term “about” to describe the high and low values are also implicitly modified by that term, unless otherwise specified.

Claims
  • 1. A sealant composition comprising: a base composition comprising a sulfur-containing polymer;a curing agent composition comprising a curing agent; andan electrically conductive filler in at least one of the base composition or the curing agent composition, the electrically conductive filler comprising carbon nanotubes and stainless steel fibers; wherein the stainless steel fibers have an average particle dimension larger than an average particle dimension of the carbon nanotubes wherein the stainless steel fibers have an average first dimension of about 8 μm to about 22 μm, and an average second dimension of about 330 μm to about 1 mm.
  • 2. The sealant composition of claim 1, wherein the electrically conductive filler is in the base composition.
  • 3. The sealant composition of claim 1, wherein the electrically conductive filler is in the curing agent composition.
  • 4. The sealant composition of claim 1, wherein the electrically conductive filler is in both the curing agent composition and the base composition.
  • 5. The sealant composition of claim 1, wherein the sealant composition is substantially nickel free.
  • 6. The sealant composition of claim 1, wherein the carbon nanotubes have an average length dimension of about 5 μm to about 30 μm, and an average diameter dimension of about 10 nm to about 30 nm.
  • 7. The sealant composition of claim 1, wherein a volume ratio of the carbon nanotubes to the stainless steel fibers is about 1:5 to 1:50.
  • 8. The sealant composition of claim 1, further comprising at least one of an adhesion promoter, a corrosion inhibitor or a plasticizer in at least one of the base composition or the curing agent composition.
  • 9. The sealant composition of claim 1, wherein the sulfur-containing polymer is a polysulfide or a polythioether.
  • 10. A sealant composition comprising: a base composition comprising a sulfur-containing polymer;a curing agent composition comprising a curing agent; andan electrically conductive filler in at least one of the base composition or the curing agent composition, the electrically conductive filler comprising carbon nanotubes and stainless steel fibers; wherein the carbon nanotubes have an average particle dimension larger than an average particle dimension of the stainless steel fibers wherein the stainless steel fibers have an average first dimension of about 8 μm to about 22 μm, and an average second dimension of about 330 μm to about 1 mm.
  • 11. The sealant composition of claim 10, wherein the electrically conductive filler is in the base composition.
  • 12. The sealant composition of claim 10, wherein the electrically conductive filler is in the curing agent composition.
  • 13. The sealant composition of claim 10, wherein the electrically conductive filler is in both the curing agent composition and the base composition.
  • 14. The sealant composition of claim 10, wherein the sealant composition is substantially nickel free.
  • 15. The sealant composition of claim 10, wherein the carbon nanotubes have an average length dimension of about 5 μm to about 30 μm, and an average diameter dimension of about 10 nm to about 30 nm.
  • 16. The sealant composition of claim 10, wherein a volume ratio of the carbon nanotubes to the stainless steel fibers is about 1:5 to 1:50.
  • 17. The sealant composition of claim 10, further comprising at least one of an adhesion promoter, a corrosion inhibitor or a plasticizer in at least one of the base composition or the curing agent composition.
  • 18. The sealant composition of claim 10, wherein the sulfur-containing polymer is a polysulfide or a polythioether.
  • 19. A sealant composition comprising: a substantially nickel-free base composition comprising a sulfur-containing polymer;a substantially nickel-free curing agent composition comprising a curing agent; anda substantially nickel-free electrically conductive filler in at least one of the base composition or the curing agent composition, the electrically conductive filler comprising carbon nanotubes and stainless steel fibers; wherein the stainless steel fibers have an average particle dimension larger than an average particle dimension of the carbon nanotubes fibers wherein the stainless steel fibers have an average first dimension of about 8 μm to about 22 μm, and an average second dimension of about 330 μm to about 1 mm.
  • 20. The sealant composition of claim 19, wherein the carbon nanotubes have an average length dimension of about 5 μm to about 30 μm, and an average diameter dimension of about 10 nm to about 30 nm.
  • 21. The sealant composition of claim 19, wherein a volume ratio of the carbon nanotubes to the stainless steel fibers is about 1:5 to 1:50.
  • 22. A sealant composition comprising: a substantially nickel-free base composition comprising a sulfur-containing polymer;a substantially nickel-free curing agent composition comprising a curing agent; anda substantially nickel-free electrically conductive filler in at least one of the base composition or the curing agent composition, the electrically conductive filler comprising carbon nanotubes and stainless steel fibers; wherein the carbon nanotubes have an average particle dimension larger than an average particle dimension of the stainless steel fibers wherein the stainless steel fibers have an average first dimension of about 8 μm to about 22 μm, and an average second dimension of about 330 μm to about 1 mm.
  • 23. The sealant composition of claim 22, wherein the carbon nanotubes have an average length dimension of about 5 μm to about 30 μm, and an average diameter dimension of about 10 nm to about 30 nm.
  • 24. The sealant composition of claim 22, wherein a volume ratio of the carbon nanotubes to the stainless steel fibers is about 1:5 to 1:50.
CROSS REFERENCE TO RELATED APPLICATION

This application claims priority to and the benefit of U.S. Provisional Application Ser. No. 61/535,886, filed on Sep. 16, 2011 and entitled CONDUCTIVE SEALANT COMPOSITIONS, the entire content of which is incorporated herein by reference.

US Referenced Citations (216)
Number Name Date Kind
3782856 Salkind et al. Jan 1974 A
4156067 Gould May 1979 A
4296172 Hill Oct 1981 A
4319300 Napiorkowski et al. Mar 1982 A
4320435 Jones Mar 1982 A
4375493 George et al. Mar 1983 A
4429216 Brigham Jan 1984 A
4454379 Cleveland et al. Jun 1984 A
4478963 McGarry Oct 1984 A
4557560 Bohannon, Jr. et al. Dec 1985 A
4559112 Tamamura et al. Dec 1985 A
4601828 Gershoni Jul 1986 A
4698723 Bryan, Jr. Oct 1987 A
4724316 Morton Feb 1988 A
4752415 Iwaskow et al. Jun 1988 A
4760845 Kovalcheck Aug 1988 A
4808481 Luxon Feb 1989 A
4839771 Covey Jun 1989 A
4882089 Iwaskow et al. Nov 1989 A
4983456 Iwaskow et al. Jan 1991 A
5115035 Shiraki et al. May 1992 A
5185654 Mosher et al. Feb 1993 A
5225265 Prandy et al. Jul 1993 A
5273706 Laughner Dec 1993 A
5284888 Morgan Feb 1994 A
5298708 Babu et al. Mar 1994 A
5314309 Blakeley et al. May 1994 A
5352254 Celikkaya Oct 1994 A
5354499 Elliott Oct 1994 A
5370921 Cedarleaf Dec 1994 A
5401901 Gerry et al. Mar 1995 A
5417743 Dauber May 1995 A
5422423 Shacklette et al. Jun 1995 A
5431974 Pierce Jul 1995 A
5490893 Enlow et al. Feb 1996 A
5560934 Afzali-Ardakani et al. Oct 1996 A
5570265 Smith Oct 1996 A
5603514 Jencks et al. Feb 1997 A
5612130 Smirnov et al. Mar 1997 A
5698316 Kuras et al. Dec 1997 A
5700743 Puchinger et al. Dec 1997 A
5725707 Koon et al. Mar 1998 A
5736603 Pfeiffer et al. Apr 1998 A
5789085 Blohowiak et al. Aug 1998 A
5810094 Kesler et al. Sep 1998 A
5814137 Blohowiak et al. Sep 1998 A
5869172 Caldwell Feb 1999 A
5870160 Yanagawa et al. Feb 1999 A
5927240 Maxon Jul 1999 A
5935698 Pannell Aug 1999 A
5939197 Blohowiak et al. Aug 1999 A
5945643 Casser Aug 1999 A
5952445 Roesler et al. Sep 1999 A
5958578 Blohowiak et al. Sep 1999 A
6037008 Huang et al. Mar 2000 A
6092350 Dumlao et al. Jul 2000 A
6099965 Tennent et al. Aug 2000 A
6127462 Chen et al. Oct 2000 A
6142595 Dellapi et al. Nov 2000 A
6159611 Lee et al. Dec 2000 A
6277916 Terbrueggen et al. Aug 2001 B1
6299716 Bettinger Oct 2001 B1
6333101 Imashiro et al. Dec 2001 B1
6483685 Ramarge et al. Nov 2002 B1
6485735 Steen et al. Nov 2002 B1
6548175 Sachdev et al. Apr 2003 B2
6548189 Gunasekaran et al. Apr 2003 B1
6612175 Peterson et al. Sep 2003 B1
6737444 Liu May 2004 B1
6790526 Vargo et al. Sep 2004 B2
6890373 Nemoto et al. May 2005 B2
6906120 Davis et al. Jun 2005 B1
6916890 Woods et al. Jul 2005 B1
7001666 Krienke et al. Feb 2006 B2
7022763 Matsugi et al. Apr 2006 B2
7056409 Dubrow Jun 2006 B2
7120004 Hall Oct 2006 B2
7258819 Harris, IV Aug 2007 B2
7276665 Rauckman et al. Oct 2007 B1
7326862 Lionetta et al. Feb 2008 B2
7371462 Tsumura et al. May 2008 B2
7494324 Hibbard Feb 2009 B2
7553553 Palumbo et al. Jun 2009 B2
7629400 Hyman Dec 2009 B2
7678997 Rawlings Mar 2010 B2
7686905 Ackerman et al. Mar 2010 B2
7730547 Barrera et al. Jun 2010 B2
7745528 Prud'Homme et al. Jun 2010 B2
7759298 Dufresne et al. Jul 2010 B2
7772499 Rauckman Aug 2010 B2
7795365 Karjala et al. Sep 2010 B2
7842246 Wohlstadter et al. Nov 2010 B2
7842387 Resasco et al. Nov 2010 B2
7867621 Rawlings et al. Jan 2011 B2
7869181 Le Jan 2011 B2
7883050 Dufresne et al. Feb 2011 B2
7959783 Byrd et al. Jun 2011 B2
8337658 Hasegawa et al. Dec 2012 B2
20010008672 Norvell et al. Jul 2001 A1
20020004132 Banovetz et al. Jan 2002 A1
20020038135 Connelly et al. Mar 2002 A1
20020108699 Cofer et al. Aug 2002 A1
20020132075 Friend et al. Sep 2002 A1
20030055149 McGee Mar 2003 A1
20030146346 Chapman Jr Aug 2003 A1
20030152766 Vargo et al. Aug 2003 A1
20030173460 Chapman, Jr. Sep 2003 A1
20030216662 Jersey-Willuhn et al. Nov 2003 A1
20030220432 Miller et al. Nov 2003 A1
20040009344 Krienke et al. Jan 2004 A1
20040099659 Johnson, Jr. May 2004 A1
20040100764 Hanson et al. May 2004 A1
20040126504 Ouchi et al. Jul 2004 A1
20040220327 Cosman et al. Nov 2004 A1
20050025967 Lawton et al. Feb 2005 A1
20050031843 Robinson et al. Feb 2005 A1
20050062024 Bessette et al. Mar 2005 A1
20050088097 Bae et al. Apr 2005 A1
20050181203 Rawlings et al. Aug 2005 A1
20050197447 Gu et al. Sep 2005 A1
20050197450 Amano et al. Sep 2005 A1
20050218398 Tran Oct 2005 A1
20050225751 Sandell et al. Oct 2005 A1
20050266238 Amano et al. Dec 2005 A1
20060035054 Stepanian et al. Feb 2006 A1
20060046005 McGee Mar 2006 A1
20060062983 Irvin et al. Mar 2006 A1
20060100368 Park May 2006 A1
20060110599 Honma et al. May 2006 A1
20060182949 Salnikov et al. Aug 2006 A1
20060182950 Yun et al. Aug 2006 A1
20060188580 Sacks Aug 2006 A1
20060193789 Tamarkin et al. Aug 2006 A1
20060274047 Spath et al. Dec 2006 A1
20060274048 Spath et al. Dec 2006 A1
20060281219 Trezza Dec 2006 A1
20060285813 Ferguson Dec 2006 A1
20070012111 Kim Jan 2007 A1
20070193770 Ueno et al. Aug 2007 A1
20070230131 Bunyan et al. Oct 2007 A1
20070241303 Zhong et al. Oct 2007 A1
20070275623 Mussig Nov 2007 A1
20070281116 Matviya et al. Dec 2007 A1
20070281163 Matviya et al. Dec 2007 A1
20070281570 Liggett et al. Dec 2007 A1
20070292622 Rowley et al. Dec 2007 A1
20070298669 Barrera et al. Dec 2007 A1
20080020275 Koh et al. Jan 2008 A1
20080047894 Trogolo et al. Feb 2008 A1
20080057265 Liang et al. Mar 2008 A1
20080075954 Wardle et al. Mar 2008 A1
20080078576 Blacker et al. Apr 2008 A1
20080083721 Kaiserman et al. Apr 2008 A1
20080085405 Prenzel et al. Apr 2008 A1
20080102279 Ito et al. May 2008 A1
20080128430 Kovach et al. Jun 2008 A1
20080146480 Dufresne et al. Jun 2008 A1
20080152949 Mevellec et al. Jun 2008 A1
20080159871 Bech Jul 2008 A1
20080166563 Brittingham et al. Jul 2008 A1
20080169521 Foster et al. Jul 2008 A1
20080294220 Stevenson et al. Nov 2008 A1
20080302561 Prud'Homme et al. Dec 2008 A1
20090029147 Tang et al. Jan 2009 A1
20090035469 Sue et al. Feb 2009 A1
20090050735 Sobol Feb 2009 A1
20090054272 Prud'Homme et al. Feb 2009 A1
20090104361 Ma et al. Apr 2009 A1
20090118420 Zou et al. May 2009 A1
20090127514 Korkut et al. May 2009 A1
20090220794 O'Neill et al. Sep 2009 A1
20090223629 Cosman et al. Sep 2009 A1
20090236569 Pike-Biegunski et al. Sep 2009 A1
20090321238 Nhan et al. Dec 2009 A1
20100000754 Mann et al. Jan 2010 A1
20100001512 Breay et al. Jan 2010 A1
20100041297 Jiang et al. Feb 2010 A1
20100046170 Stevenson et al. Feb 2010 A1
20100061678 Swinehart et al. Mar 2010 A1
20100086706 Everaerts et al. Apr 2010 A1
20100086729 Long Apr 2010 A1
20100089002 Merkel Apr 2010 A1
20100096181 Nakamura et al. Apr 2010 A1
20100096595 Prud'Homme et al. Apr 2010 A1
20100096597 Prud'Homme et al. Apr 2010 A1
20100104854 Takada et al. Apr 2010 A1
20100116527 Khosla et al. May 2010 A1
20100122832 Bukshpun et al. May 2010 A1
20100136327 Ma et al. Jun 2010 A1
20100165276 David et al. Jul 2010 A1
20100178487 Arai et al. Jul 2010 A1
20100182679 Han et al. Jul 2010 A1
20100209690 Sang et al. Aug 2010 A1
20100210745 McDaniel et al. Aug 2010 A1
20100220074 Irvin, Jr. et al. Sep 2010 A1
20100239871 Scheffer et al. Sep 2010 A1
20100276630 Chandrasekhar et al. Nov 2010 A1
20100276645 Aspin et al. Nov 2010 A1
20100282470 Alberty et al. Nov 2010 A1
20100321897 Hill et al. Dec 2010 A1
20110001086 Kruckenberg et al. Jan 2011 A1
20110036726 Majima et al. Feb 2011 A1
20110049292 Kruckenberg et al. Mar 2011 A1
20110086206 Scheffer et al. Apr 2011 A1
20110088931 Lettow et al. Apr 2011 A1
20110117202 Bourke, Jr. et al. May 2011 A1
20110123906 Wang et al. May 2011 A1
20110133132 Zhamu et al. Jun 2011 A1
20110133134 Varma et al. Jun 2011 A1
20110135921 Tse et al. Jun 2011 A1
20110135925 Zhamu et al. Jun 2011 A1
20110147674 Arai et al. Jun 2011 A1
20110154948 Chung et al. Jun 2011 A1
20110164987 Grabau Jul 2011 A1
20110171469 Shah et al. Jul 2011 A1
20110180524 Brittingham et al. Jul 2011 A1
Foreign Referenced Citations (145)
Number Date Country
P10815686-7 Dec 2010 BR
2 084 626 Jun 1993 CA
2 502 128 Sep 2005 CA
1049021 Feb 1991 CN
101192669 Jun 2008 CN
101237723 Aug 2008 CN
101241803 Aug 2008 CN
101409336 Apr 2009 CN
101587992 Nov 2009 CN
101694818 Apr 2010 CN
101771915 Jul 2010 CN
101794671 Aug 2010 CN
101798882 Aug 2010 CN
101844757 Sep 2010 CN
101916633 Dec 2010 CN
20 2004 009 060 Sep 2004 DE
20 2004 009 061 Sep 2004 DE
10 2007 051 797 Jun 2009 DE
0 126 494 Nov 1984 EP
0 139 667 May 1985 EP
0 142 857 May 1985 EP
0 145 400 Jun 1985 EP
0 167 042 Jan 1986 EP
0 172 039 Feb 1986 EP
0 173 303 Mar 1986 EP
0 177 289 Apr 1986 EP
0 177 579 Apr 1986 EP
0 182 809 Jun 1986 EP
0 183 782 Jun 1986 EP
0 184 829 Jun 1986 EP
0 191 191 Aug 1986 EP
0 191 491 Aug 1986 EP
0 192 199 Aug 1986 EP
0 192 199 Aug 1986 EP
0 194 865 Sep 1986 EP
0 205 815 Dec 1986 EP
0 206 170 Dec 1986 EP
0 206 172 Dec 1986 EP
0 207 236 Jan 1987 EP
0 208 789 Jan 1987 EP
0 211 104 Feb 1987 EP
0 212 970 Mar 1987 EP
0 213 737 Mar 1987 EP
0 217 334 Apr 1987 EP
0 223 408 May 1987 EP
0 223 564 May 1987 EP
0 224 122 Jun 1987 EP
0 224 795 Jun 1987 EP
0 230 501 Aug 1987 EP
0 233 651 Aug 1987 EP
0 234 385 Sep 1987 EP
0 234 720 Sep 1987 EP
0 239 915 Oct 1987 EP
0 240 083 Oct 1987 EP
0 240 163 Oct 1987 EP
0 245 710 Nov 1987 EP
0 246 337 Nov 1987 EP
0 247 692 Dec 1987 EP
0 252 288 Jan 1988 EP
0 266 879 May 1988 EP
0 276 506 Aug 1988 EP
0 281 236 Sep 1988 EP
0 437 979 Jul 1991 EP
0 550 846 Jul 1993 EP
0 632 688 Jan 1995 EP
0 730 017 Sep 1996 EP
0 790 182 Aug 1997 EP
0 811 480 Dec 1997 EP
0 814 183 Dec 1997 EP
1 055 512 Nov 2000 EP
1 134 069 Sep 2001 EP
1 593 293 BI Nov 2005 EP
1 692 752 Aug 2006 EP
1 845 296 Apr 2007 EP
1 926 591 BI Jun 2008 EP
2 399 739 Dec 2011 EP
1 143 314 Feb 1969 GB
2 410 308 Jul 2005 GB
60-171247 Sep 1985 JP
60-243170 Dec 1985 JP
05-156100 Jun 1993 JP
2001-172582 Jun 2001 JP
2003-092205 Mar 2003 JP
2008-207404 Sep 2008 JP
2008-218712 Sep 2008 JP
2008-251715 Oct 2008 JP
2008-284191 Nov 2008 JP
2009-043672 Feb 2009 JP
2009-272454 Nov 2009 JP
2010-131789 Jun 2010 JP
2010-131888 Jun 2010 JP
2010-194749 Sep 2010 JP
2010-248605 Nov 2010 JP
2010-260174 Nov 2010 JP
2011-042030 Mar 2011 JP
2011-142024 Jul 2011 JP
10-2007-0003264 Jan 2007 KR
WO 8102895 Oct 1981 WO
WO 8803543 May 1988 WO
WO 9101621 Feb 1991 WO
WO 9403743 Feb 1994 WO
WO 9423679 Oct 1994 WO
WO 9623837 Aug 1996 WO
WO 9706649 Feb 1997 WO
WO 9718081 May 1997 WO
WO 9908298 Feb 1999 WO
WO 9913812 Mar 1999 WO
WO 9931176 Jun 1999 WO
WO 9946348 AI Sep 1999 WO
WO 0022226 Apr 2000 WO
WO 0049669 Aug 2000 WO
WO 0117850 Mar 2001 WO
WO 0163984 Aug 2001 WO
WO 0177185 Oct 2001 WO
WO 0224383 Mar 2002 WO
WO 02093696 Nov 2002 WO
WO 2004045369 Jun 2004 WO
WO 2005019297 Mar 2005 WO
WO 2005106153 Nov 2005 WO
WO 2006040754 Apr 2006 WO
WO 2006040754 Apr 2006 WO
WO 2007015710 Feb 2007 WO
WO 2007022106 Feb 2007 WO
WO 2007050725 May 2007 WO
WO 2008056122 May 2008 WO
WO 2008106143 Sep 2008 WO
WO 2008115883 Sep 2008 WO
WO 2009012618 Jan 2009 WO
WO 2009051411 Apr 2009 WO
WO 2009052817 Apr 2009 WO
WO 2009086161 Jul 2009 WO
WO 2009087372 Jul 2009 WO
WO 2009105036 Aug 2009 WO
WO 2009111744 Sep 2009 WO
WO 2009115488 Sep 2009 WO
WO 2010024564 Mar 2010 WO
WO 2010035087 Apr 2010 WO
WO 2010036563 Apr 2010 WO
WO 2010051102 May 2010 WO
WO 2010093598 Aug 2010 WO
WO 2010095536 Aug 2010 WO
WO 2010147982 Dec 2010 WO
WO 2011036689 Mar 2011 WO
WO 2011041781 Apr 2011 WO
WO2011081249 Jul 2011 WO
Non-Patent Literature Citations (41)
Entry
Donaldson, Ken Poland, Craig Duffin, Rodger Bonner, James. (2012). Toxicology of Carbon Nanotubes—1.6.1 Carbon Nanotube Composites. Cambridge University Press. Online version available at: http://app.knovel.com/hotlink/pdf/id:kt00ARNBT1/toxicology-carbon-nanotubes/carbon-nanotube-composites.
Enos, D.G., “Understanding the Atmospheric Degradation of Noble Metal-Plated Connector Materials,” Corrosion, vol. 66, No. 10, Oct. 2010, pp. 105003-1-105003-12.
Dorworth, Louis C., “Repair of Lightning Strike Protection on CFRP Sandwich Structures Using Mesh-Embedded-Syntactic Materials,” SAMPE Conference Proceedings (2006) vol. 51, pp. 329-1-329/14.
Ransom, Joy, et al., “Laboratory Testing to Validate Expanded Products for Use in Holes in Composite Structure Joining Applications,” SAMPE Conference Proceedings (2008) vol. 53, pp. 70/1-70/16.
Hansen, George, et al., “Electrically Conductive Putty-Type Repair System for Composite Structures,” Sampe Conference Proceedings (2007) vol. 52, pp. 266/1-266/15.
Suchentrunk, Richard, et al., “Coatings on Composites—New Developments and Applications in the Aerospace Industry,” Report (1992), MBB-Z-0443-92-PUB, ETN-93-93444, Sci. Tech. Aerosp. Rep. 1993, 31(7) 29 pgs.
Johnson, C. J., et al., “CFRP Blistering Induced by Phosphate-fluoride Coated Titanium Fasteners,” Proc. ADVMAT/91, International Symposium Environ. Eff. Adv. Mater., 1st (1992), Meeting Date 1991, pp. 6/1-6/4.
Chung, D. D. L., et al., “Strengthening Graphite-Polymer Composites by Using Intercalated Graphite,” Interface in Polymer, Ceramic, and Metal Matrix Composites; Cleveland, Ohio; Jun. 13, 1988, Conference Paper, pp. 101-105.
Griffin, Charles F., “Fuel Containment and Damage Tolerance in Large Composite Primary Aircraft Structures,” NASA Contractor Report 166083; Contract NASI-16856, Mar. 1983, 15pgs.
Brick, R. O., et al., “The Significance of Advanced Structural Fabrication Techniques on Aircraft Lightning Protection,” Society of Automotive Engineers, Document 680290, 1968, pp. 923-931.
Prandy, J. M., et al., “Environmentally Durable Lightning Strike Protection Materials for Composites,” 37th International SAMPE Symposium, Mar. 9-12, 1992, pp. 78-87.
Guillaumon, Jean-Claude, “New Developments in Thermo-Optical Coatings for Space Vehicles Antistatic and Lightening Paints for Launchers,” IAF, Int'l Astronautical Congress, 40th, Malaga, Spain; Oct. 7-13, 1989, 5 pgs.
Guerard, Francoise, et al., “New Developments in Thermo-Optical Coatings for Space Vehicles,” European Symposium on Spacecraft Materials in Space Environment, 4th, Toulouse, France; Sep. 6-9, 1988, pp. 549-562.
Billias, Michael G., et al., “Electrically Conductive Structural Adhesive,” 30th National SAMPE Symposium and Exhibition, vol. 30; Anaheim, California; Mar. 19-21, 1985, cover page and pp. 1397-1407 (12 pgs.).
Pachamuthu, Ashok, et al., “Enhancement of Electrical and Thermal Conductivity of Conductive Coatings and Adhesives by Addition of Nanometer Sized Particles,” Materials Science and Technology (MS&T) 2006: Materials and Systems vol. 2, pp. 327-332.
Kim, Woon-Soo, et al., “Electrical Properties of PVdF/PVP Composite Filled with Carbon Nanotubes Prepared by Floating Catalyst Method,” Macromolecular Research, vol. 10, No. 5, pp. 253-258 (2002).
Huang, Chi-Yuan, et al., “The manufacture and investigation of multi-walled carbon nanotube/polypyrrole/ EVA nano-polymeric composites for electromagnetic interference shielding,” Thin Solid Films, vol. 519 (2011) pp. 4765-4773.
Lee, Eun-Je, et al., “Resistivity and crystallization behavior of saponified EVA/carbon black and EVA/graphite composites,” Abstracts of Papers, 241st ACS National Meeting & Exposition, Anaheim, CA; Mar. 27-31, 2011, PMSE-176. American Chemical Society: Washington, D.C. (1 pg.).
Rahaman, M., et al., “Development of high performance EMI shielding material from EVA, NBR, and their blends: effect of carbon black structure,” Journal of Materials Science, (2011) vol. 46, pp. 3989-3999.
Thomassin, J. -M., et al., “Polymer/carbon nanotube composites for electromagnetic interference reduction,” Physical Properties and Applications of Polymer Nanocomposites, (2010) pp. 563-587.
Sarlin, Juha, et al., “PP composites with Hybrid Nanofillers: NTC phenomenon,” AIP Conference Proceedings (2010), CP1255, Vth International Conference on Times of Polymers (TOP) and Composites, cover page and pp. 85-88 (5 pgs.).
Al-Saleh, Mohammed H., et al., “Processing-microstructure-property relationship in conductive polymer nanocomposites,” Polymer, vol. 51 (2010) pp. 2740-2747.
Ray, Moumita, et al., “An Investigation of the Electromagnetic Shielding Effectiveness of Ethylene Vinyl Acetate Elastomer Reinforced With Carbon Nanofillers,” Polymers & Polymer Composites, (2010) vol. 18, No. 2, pp. 59-65.
Saini, Parveen, et al., “Polyaniline-MWCNT nanocomposites for microwave absorption and EMI shielding,” Materials Chemistry and Physics, vol. 113 (2009) pp. 919-926.
Al-Saleh, Mohammed H., et al., “A review of vapor grown carbon nanofiber/polymer conductive composites,” Carbon, vol. 47 (2009) pp. 2-22.
Bourdo, Shawn, et al., “Structural, Electrical, and Thermal Behavior of Graphite-Polyaniline Composites with Increased Crystallinity,” Advanced Functional Materials, 2008, vol. 18, pp. 432-440.
Mohanraj, G. T., et al., “AC Impedance Analysis and EMI Shielding Effectiveness of Conductive SBR Composites,” Polymer Engineering and Science, (2006) vol. 46, No. 10, pp. 1342-1349.
Ou, Runqing, et al., “Low Percolation Threshold Composites Consisting of PMMA and Carbon Black,” School of Materials Science and Engineering, TMS Letters, (2005) vol. 2, pp. 117-118.
El-Tantawy, Farid, “Development of Novel Functional Conducting Elastomer Blends Containing Butyl Rubber and Low-Density Polyethylene for Current Switching, Temperature Sensor, and EMI Shielding Effectiveness Applications,” Journal of Applied Polymer Science, (2005) vol. 97, pp. 1125-1138.
Heiser, Jessica A., et al., “Shielding Effectiveness of Carbon-Filled Nylon 6,6,” Polymer Composites, Aug. 2004, vol. 25, No. 4, pp. 407-416.
Das, N. C., et al., “Electromagnetic Interference Shielding Effectiveness of Hybrid Conductive Polymer Composite,” Journal of Elastomers and Plastics, vol. 34, Jul. 2002, pp. 199-223.
Clingerman, Matthew L., et al., “Synergistic Effects of Carbon Fillers in Electrically Conductive Nylon 6,6 and Polycarbonate Based Resins,” Polymer Composites, Oct. 2002, vol. 23, No. 5, pp. 911-924.
Rimska, Zdaka, et al., “AC Conductivity of Carbon Fiber-Polymer Matrix Composites at the Percolation Threshold,” Polymer Composites, Feb. 2002, vol. 23, No. 1, pp. 95-103.
Das, N. C., et al., “Electromagnetic Interference Shielding Effectiveness of Conductive Carbon Black and Carbon Fiber-Filled Composites Based on Rubber and Rubber Blends,” Advances in Polymer Technology, vol. 20, No. 3, pp. 226-236 (2001).
Das, N. C., et al., “Electromagnetic Interference Shielding Effectiveness of Ethylene Vinyl Acetate Based Conductive Composites Containing Carbon Fillers,” Journal of Applied Polymer Science, vol. 80, pp. 1601-1608 (2001).
Das, N. C., et al., “Electromagnetic interference shielding effectiveness of carbon black and carbon fibre filled EVA and NR based composites,” Composites Part A: Applied Science and Manufacturing, vol. 31 (2000) pp. 1069-1081.
Patel, Niraj, “New Thermoplastic Resin Compounds Utilizing Highly Efficient Conductive Filler System,” General Electric Company, Annual Technical Conference—Society of Plastics Engineers (2000), 58th (vol. 2), 5 pgs.
Sau, K. P., et al., “Electromagnetic interference shielding by carbon black and carbon fibre filled rubber composites,” Plastics, Rubber and Composites Processing and Applications, 1997, vol. 26, No. 7, pp. 291-297.
Praminik, P. K., et al., “Electromagnetic Interference Shielding by Conductive Nitrile Rubber Composites Containing Carbon Fillers,” Journal of Elastomers and Plastics, vol. 23, Oct. 1991, pp. 345-361.
Crosby, J. M., et al., “Conductive thermoplastic composites,” Rubber World, Nov. 1985, pp. 30-33.
Bigg, D. M., “An Investigation of the Effect of Carbon Black Structure, Polymer Morphology, and Processing History on the Electrical Conductivity of Carbon-Black-Filled Thermoplastics,” Journal of Rheology, (1984) vol. 28, No. 5, pp. 501-516.
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20130075668 A1 Mar 2013 US
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61535886 Sep 2011 US