CONDUCTIVE CARBON FIBER-BASED SPONGE
20210122895 · 2021-04-29
Inventors
- Ashwati Krishnan (Pittsburgh, PA, US)
- Pulkit Grover (Pittsburgh, PA, US)
- Shawn Kelly (Pittsburgh, PA, US)
- Ritesh Kumar (Pittsburgh, PA, US)
- Kalee Rozylowicz (Pittsburgh, PA, US)
Cpc classification
A61N1/0476
HUMAN NECESSITIES
C08K2201/003
CHEMISTRY; METALLURGY
C08J2207/10
CHEMISTRY; METALLURGY
A61N1/0452
HUMAN NECESSITIES
A61N1/0456
HUMAN NECESSITIES
C08J9/286
CHEMISTRY; METALLURGY
C08J2205/052
CHEMISTRY; METALLURGY
H01B1/04
ELECTRICITY
International classification
C08J9/00
CHEMISTRY; METALLURGY
C08J9/28
CHEMISTRY; METALLURGY
Abstract
A carbon fiber-based conductive sponge for low electrode-skin impedance biosignal recordings is described. When the sponge is used with water or saline solution, no gel is required, drastically lowering the setup time for EEGs compared to classical wet electrodes. The wet sponges achieve an electrode-skin impedance as low as 2.5 kΩ¶ when wet, making them better than state of the art gel electrodes. Additionally, even as the sponge dries, it continues to remain conductive and performs as a reliable dry electrode.
Claims
1. A conductive sponge comprising: a sponge body comprising a hydrophilic material; and a plurality of carbon fibers or carbon nanofibers dispersed throughout the sponge body.
2. The conductive sponge of claim 1 wherein the hydrophilic material is hydrophilic polyurethane foam or cellulose.
3. The conductive sponge of claim 2 further comprising: adding a surfactant to the hydrophilic material.
4. A conductive sponge comprising: a sponge body comprising a silicone foam: and a plurality of carbon fibers dispersed throughout the sponge body.
5. The conductive sponge of claim 4 wherein the plurality of carbon fibers comprises between 5% and 12% of the total weight of the conductive sponge.
6. The conductive sponge of claim 4 wherein the silicone foam is a closed-cell foam.
7. The conductive sponge of claim 4 wherein the carbon fibers range in length from approximately 2 mm to approximately 5 mm.
8. The conductive sponge of claim 4 wherein a majority of the carbon fibers are between 2 mm and 5 mm in length.
9. The conductive sponge of claim 4 wherein the carbon fibers are approximately 5 microns in diameter.
10. The conductive sponge of claim 4 wherein the conductive sponge is conductive when dry.
11. A conductive sponge comprising: a sponge body comprising a hydrophilic material or a silicone foam; and a plurality of carbon nanofibers dispersed throughout the sponge body.
12. A process for manufacturing a conductive sponge comprising: mixing a plurality of carbon fibers or carbon nanofibers into an uncured silicon foam or a hydrophilic polyurethane pre-polymer to create a homogenous mixture; mixing a curing agent to the homogeneous mixture of uncured silicone foam and carbon fibers, or mixing surfactant and water with the homogenous polyurethane mixture; and pouring the mixture into a mold for curing.
13. The process of claim 12 further comprising adding a thinning agent to the homogenous silicone mixture prior to the pouring of the mixture into a mold.
14. The process of claim 12 further comprising shaving a layer from one or more surfaces of the cured conductive sponge to expose the carbon fibers.
15. The process of claim 12 wherein a majority of the carbon fibers are between 2 mm and 5 mm in length, or wherein the majority of the carbon nanofibers are 50-200 microns in length.
16. The process of claim 12 wherein the carbon fibers are approximately 5 microns in diameter, or carbon nanofibers are approximately 0.1 microns in diameter
17. The process of claim 12 wherein the carbon fibers comprise between 5% and 12% of the total weight of the conductive sponge.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0012]
[0013]
[0014]
[0015]
[0016]
[0017]
[0018]
DETAILED DESCRIPTION OF THE INVENTION
Preparation of the Conductive Sponge
[0019] In certain embodiments of the invention, a two-part curable silicone foam was used as the sponge medium. Such foam can be obtained, for example, from Smooth-On Inc. of Macungie, Pa. USA, having a brand name of “Soma Foama 15”. Alternatively, hydrophilic pre-polymers from Carpenter Chemicals of Richmond, Va. USA, can be used, which can be cured upon the addition of water. The carbon fiber (CF) may be obtained, for example, from ACP Composites of Livermore. Calif. USA, and typically, a majority of the carbon fibers should be 2-5 mm in length. Alternatively, carbon nanofibers (CNF) can also be used (for example, procured from Pyrograf-III Carbon Nanofiber, Cedarville. Ohio. USA). A majority the Carbon nanofibers should have a diameter of 70-200 nm and a length of 50-200 microns
[0020] The silicone foam comes as a two-part preparation, having a Part A being the silicone foam and a Part B being a curing agent. Part A of the two-part silicone foam is thoroughly mixed with the CF at 25° C. in the ratios presented in Table 1 to create a homogenous mixture. Silicone thinning fluid sourced from Hager Plastics of Chicago. Ill. USA, may be added to allow for better flow of the mixture for molding. For the hydrophilic polyurethane, the pre-polymer requires a surfactant that binds with the isocyanate in the polymer to make it more water absorbent. Lauramine oxide and or propylene glycol, a surfactant commonly found in soaps, can be added to the pre polymer before curing. The carbon nanofibers are added thoroughly mixed with the pre polymer before the addition of water.
[0021] After thorough mixing, Part B of the silicone foam was added to the Part A-CF blend, stirred and immediately poured into molds to cure. The time taken for the mixture to become a solid foam (cure time) is 1 hour at room temperature. Table 1 shows variations in preparations in different samples for silicone. For the hydrophilic polyurethane sponge, water is added to the pre-polymer-CNF-surfactant mixture and immediately poured into a mold for curing. The time take for curing is about 1 hour at room temperature. Table 2 shows variations for different samples of polyurethane.
TABLE-US-00001 TABLE 1 Silicone formulations Silicone (g) Carbon Fiber # Part A Part B Thinning Fluid (g) I 3.11 1.5 0.7 0.2 II 3.07 1.5 0.62 0.25 III 4 2 0.2 0.6 IV 4.06 2.1 0.7 0.81
TABLE-US-00002 TABLE 2 Hydrophilic Polyurethane formulations Hydrophlic Polyurethane Prepolymer Surfactant Water CNF I 3 0.5 4.5 1 II 4.5 0.75 9 1 III 4.3 0.9 4.3 0.9
Foam Preparation
[0022] Foams can be open-cell or closed-cell. Open-cell foams have many interconnected pores, which retain fluid to create an aqueous electrode environment that is required for low electrode-skin impedance. However, most silicone foams are closed-cell foams.
[0023] Soma Foama 15 is a closed-cell silicone foam that expands to 4 times its volume through the release of gas bubbles, creating pores. Interior pores can be opened up by applying pressure to the cured foam, or hydrophilic polymers can be used so that the sponge is absorbent.
[0024] In alternate embodiments of the invention, different materials may be used for the sponge medium. Any hydrophilic material should be suitable for use as a sponge material. For purposes of use as an EEG electrode, it is preferable that the material be bio-compatible. Preferably, the hydrophilic material starts in liquid form such that the carbon fibers can be mixed in to create a homogenous mixture of the sponge material and the carbon fibers. Thereafter, the sponge material may be solidified in any required way, such as by drying, heating or curing. In certain embodiments of the invention, the hydrophilic material may be a hydrophilic polyurethane foam (described) or a cellulose sponge. In these embodiments, a surfactant may be used to make the polyurethane foam or cellulose more hydrophilic.
[0025] The carbon fiber needs to be mixed until the Pan A-CF blend appears homogeneous (in the case of Soma Foama 15 with a shiny grey texture). This is because conduction in the silicone occurs through interconnected fibers that separate while mixing Graphite powder or milled carbon fiber was not as effective in increasing the conductivity of the silicone foam. Once the sample has cured, about 1 mm of all surfaces needed to be cut or filed to expose these fibers to metal contacts.
[0026] Chopped carbon fibers of length ˜6 mm are commercially available. However, this length makes the silicone-CF mixture difficult to pour into molds because it behaves like a flat sheet, rather than a pourable mixture. The pot life (the time elapsed before the mixture starts to cure) of Soma Foama 15 is 30 seconds. Thus, it needs to be poured immediately after mixing in Part B, and this can be accomplished more reliably with shorter carbon fibers or carbon nano-fibers.
[0027] The CF changes the mechanical properties of the resulting foam. If too much CF is added, the resulting mixture is too heavy to expand into a foam with many pores. In such cases, CNF max prove to be more reliable. There is a trade-off between foam expansion and electrical conduction.
Material Properties
[0028] The material characteristics shown here are relevant to EEG recordings. Table 1 shows a comparison of the conductivity of the CF sponge, and the extent of water retention for various mixture ratios.
Conductivity
[0029] The conductivity of bulk materials is obtained by measuring the resistance of a sample of known geometry by forcing a current through one pair of leads and measuring the voltage through another pair. 3D printed rectangular molds were used to study the conductivity of the CF sponge. The conductivity was measured using a Keithley 2400 source-meter (Tektronix, Inc., Beaverton, Oreg. USA) and was measured when the CF sponge was dry as well as after absorbing 0.9% w/v saline solution, which has a conductivity of 14.7 milli-Siemens per centimeter.
[0030]
where the variable notations are provided in
[0031] The results of the tests are shown in
Water Retention
[0032] The samples shown in Table 1 were squeezed in de-ionized water, dabbed on a clean paper towel to remove the excess drip and placed in a standard temperature and pressure environment. The samples were weighed repeatedly over 10 hours to observe the extent of evaporation over time. Similar plots may be obtained for the hydrophilic polyurethane sponge formulations in Table 2.
[0033] To evaluate the extent of liquid retention, the rate of evaporation of de-ionized water in a few silicone samples over several hours was measured, and the results are shown in
Human Scalp Measurements
[0034] To evaluate the efficacy of the conductive carbon fiber silicone sponge electrodes for biosignal acquisition applications, impedance measurements and EEG recordings on a human participant were performed. Electrode-skin impedance measurements were performed using the Intan Recording Controller (Los Angeles, Calif., USA) A sampling rate of 20 kilosamples/sec, bandpass filter settings of 0.1 Hz to 7.5 kHz and a notch filter setting at 60 Hz were used. Conductive sponge electrodes in wet and dry conditions were compared to a Covidien Kendall (Minneapolis, Minn. USA) disposable hydrogel electrode, a BrainVision (M01Tisville, N.C. USA) fiat, metal passive dry electrode and a gold-cup electrode (Natus Neurology, Pleasanton, Calif. USA) (
[0035] The diameter of all electrodes was between 8-10 mm and the thickness of the conductive carbon fiber-based sponge electrodes was 2-4 mm. For these experiments, one electrode of each of the 4 types was placed close together on the left and right sides of the forehead.
Electrode-Skin Impedance
[0036] While electrode impedance values are typically reported at 1 kHz, many relevant EEG signals are at a much lower frequency (5-40 Hz). Therefore, electrode-skin impedance was recorded at values at 20 Hz, 200 Hz, 1 kHz and 3 kHz.
[0037] The akin was not abraded for the electrodes under evaluation, however, a gold-plated cup electrode with Ten20 conductive paste was placed over abraded skin on the right mastoid bone as a reference to ensure an unbiased comparison. To verify the low impedance of the reference, an identical cup electrode configuration over the left mastoid was also used.
EEG Measurements
[0038] Alpha waves am a highly stereotypical form of EEG activity that can be measured when the participant is in a relaxed state, or when their eyes are closed 3 minutes of EEG signals from a participant were measured under two conditions: with eyes open and eyes closed. A frequency analysis of the acquired data was performed using a MATLAB-based EEGLAB toolbox.
[0039] The magnitude of the electrode-skin impedance is shown in
[0040] To demonstrate the efficacy of the conductive carbon fiber electrode material as an electrode to detect muscular activity, a time series plot is shown in
[0041] A novel carbon liber-based conductive sponge for use in biomedical applications such as EEG has been described herein. As the percentage of carbon fiber in the sponge increases, the conductivity also increases. On the other hand, the amount of solution the material can hold decreases, because there are fewer pores in the material.
[0042] A lower electrode-skin impedance was observed with a dry conductive sponge with high carbon fiber content (9-11 %). Increasing fiber content reduces the amount of time the electrode can be used as a wet electrode. The impedance of two 9 mm diameter circular carbon fiber-based sponges soaked in 0.9% w/v saline solution was tin average of 2.5 kΩ, which is better than a gold electrode with electrolyte gel. The conductive sponge electrodes (dry and wet) can reliably measure alpha waves on the forehead.
[0043] The conductive carbon-fiber sponge electrodes are a low cost, fast-installation solution for high-quality biosignal measurements. They are non-magnetic, so they can be used in conjunction with Magnetic Resonance Imaging (MRI) machines.
[0044] Because there is no electrode gel involved, the delivery of saline solution is a convenient way to achieve excellent wet electrodes within a short setup time. The purpose of using a conductive sponge is to maintain a low electrode-skin impedance even as the electrode dries out. The carbon fiber-based conductive sponge electrodes have particular applicability in portable ambulatory and low-cost high density biosignal measurement systems.