Patent Application
20160115647
1. Field of the Invention
The method of making and using an electrically conductive composite membrane relates generally to the manufacture of an electrically conductive composite membrane for water sterilization, and to its use for the electrical sterilization of water and bacterial inactivation.
2. Description of the Related Art
The lack of potable water is a major problem in many areas of the world. A wide variety of sterilization and decontamination techniques exist for producing potable water. However, most are either difficult and/or costly to implement. The use of silver membrane filters for sterilization is of interest, primarily due to its portability, but the most effective form of silver for such purposes is nanostructures embedded in an electrically conductive composite membrane. Most nano-production methods are difficult and costly to implement.
Additionally, silver alone is not optimally effective. Thus, combinations of silver nano-structures with other antimicrobial materials and techniques are of further interest. However, given that the nano-structure basis of the material is already difficult to manufacture, adding further materials and techniques compounds the difficulty in providing a cost-effective and efficient electrically conductive composite membrane filter.
Thus, a method of making and using an electrically conductive composite membrane solving the aforementioned problems is desired.
The method of making and using an electrically conductive composite membrane relates generally to the manufacture of an electrically conductive composite membrane for water sterilization, and to its use for the electrical sterilization of water and bacterial inactivation. The electrically conductive composite membrane is made from cotton fibers, graphite/carbon black and silver nanostructures. The silver nanostructures may be in the form of silver nanoparticles, silver nanowires, silver flakes, combinations thereof, or the like. The electrically conductive composite membrane is made by first dipping cotton fiber into a graphite solution to form a cotton-graphite composite fiber. The cotton-graphite composite fiber is then coated with silver nanostructures to form a cotton-graphite-silver composite material. The cotton-graphite-silver composite material may then be dipped into a solution containing a conducting polymer, and the cotton-graphite-silver composite material is formed into an electrically conductive composite membrane.
In use, the electrically conductive composite membrane is electrified by passing electrical current therethrough. Then, water to be sterilized is passed through the electrified electrically conductive composite membrane, producing potable drinking water.
These and other features of the present invention will become readily apparent upon further review of the following specification and drawings.
The sole drawing FIGURE is an environmental perspective view of a device for testing an electrically conductive composite membrane.
Similar reference characters denote corresponding features consistently throughout the attached drawings.
The method of making and using an electrically conductive composite membrane relates generally to the manufacture of an electrically conductive composite membrane for water sterilization, and to its use for the sterilization of water. The electrically conductive composite membrane is made by first dipping cotton fiber into an aqueous or non-aqueous graphite solution or suspension to form a cotton-graphite composite fiber. The cotton-graphite composite fiber is then coated with silver nanostructures to form a cotton-graphite-silver composite material. The cotton-graphite-silver composite material may then be dipped into a solution containing a conducting polymer, and the cotton-graphite-silver composite material is formed into an electrically conductive composite membrane. The conducting polymer may be polythiophene, polypyrrole, polyaniline or the like. It should be noted that the first solution (i.e., the graphite solution) is a solution of pure graphite. In other words, the graphite in the solution is not functionalized or otherwise modified, i.e., the graphite in solution is pure carbon in graphite form.
Any suitable type of silver nanostructure may be utilized, such as silver nanowires, nanoparticles or the like. In an experiment, a solution of a mixture of silver nanoparticles and nanowires was produced by first placing 30 mL of ethylene glycol in a 125 mL Erlenmeyer flask, which was then heated in an oil bath at 160° C. for 30 minutes. A 240 aliquot of an aqueous solution of 4 mM CuCl2 was then added and heated for another 15 minutes. To this reaction mixture, 9 mL of 114 mM polyvinylpyrrolidone solution was added, followed by the addition of 9 mL of freshly prepared 100 mM silver nitrate solution. The reaction continued for one additional hour, until the solution became wispy with a light brown color, indicating the formation of silver nanoparticles. The reaction was quenched by placing the flask in cold water. The silver nanoparticles and nanowires were then separated from suspension by centrifugation and washed with acetone and water. They were re-suspended in de-ionized water for further use.
Although any suitable type of natural or synthetic fiber may be utilized, such as cotton, wool, polyester, polyimide or glass fiber, cotton fiber is found to be the most effective. Similarly, although any suitable type of carbon solution or suspension may be used, graphite is found to be the most effective. As shown in Table 1 below, the artificial graphite material TC 307, manufactured by Asbury Carbons of Asbury, N.J., is found to be most effective. In Table 1, the superscript “a” refers to natural flake, the superscript “b” refers to surface enhanced synthetic graphite, the superscript “c” refers to bulk resistivity, and the superscript “d” refers to volume resistivity.
In another experiment, a 100 mg cotton sample was dipped into an aqueous solution containing the artificial graphite material TC 307. This process was repeated until a constant resistance was achieved of 30 Ω/sq. The prepared sample was then dried in an oven at 60° C. for one hour. The resultant cotton-graphite composite was dipped into an aqueous solution containing silver nanoparticles prepared as described above, and the resultant cotton-graphite-silver composite material was dried at 60° C. for one hour. The resistance of the prepared composite material was less than 0.1 Ω/sq.
It should be understood that, in the preparation, the cotton-graphite composite may be dried in air or in any inert gas, either with or without the application of vacuum, at a temperature ranging from room temperature to approximately 60° C. It should be similarly understood that following dipping into the aqueous or non-aqueous silver solution, the resultant composite fibers may be dried in air or in any inert gas, either with or without the application of vacuum, at a temperature ranging from room temperature to approximately 60° C.
Depending upon the particular method and materials, the resultant composite material is found to have a sheet resistance in the range of 0.001-100 Ω/sq. The overall silver metal content may range between approximately 0.0 and 90.0% by weight of the total composition. The resultant composite material is then formed into an electrically conductive composite membrane for water sterilization. In use, the electrically conductive composite membrane is electrified by passing electrical current therethrough. Then, water to be sterilized is passed through the electrified electrically conductive composite membrane, producing potable drinking water.
As shown in the sole FIGURE, the electrically conductive composite membrane 12 as prepared above is used as an electrode, which is positioned within a conduit, such as within exemplary funnel 14. A second conventional electrode 16 is also positioned within the funnel 14, such that potential source V generates an electrical path through the water W between electrodes 12, 16, and within the membrane electrode 12. Water passes through the membrane 12 and is collected in container 18.
In another experiment, 75 mg of the electrically conductive composite membrane was used as electrode 12, and placed in a plastic funnel with a 5 mm diameter (in the lower, thinner portion of the funnel) and with a length of 3 cm. Contaminated water samples containing a nominal E. Coli bacterial density of 107-108 CFU/ml, were passed through the membrane filter with an adjusted rate of 10 mL/min. In each experimental run, a 100 mL water sample was allowed to flow through the device 10 and the treated solution was diluted 1,000 times, from which 100 μL was plated. The device 10 was operated with an applied voltage of 20 V. The bacterial inactivation efficiency was found to be greater than 99.99% after the first run, with no E. Coli colonies observed in the second run.
The system 10 may be used for removal of common bacterial contamination of water, such as E. Coli, S. aureus, P. vulgaris and P. aeruginosa. The applied voltage is preferably in the range of ±100 V. The flow rate of the water passing through the electrically conductive composite membrane filter 12 may be between 10 and 10,000 mL/min., and the water may be passed therethrough any suitable number of times, with two or three runs being preferred.
It is to be understood that the present invention is not limited to the embodiments described above, but encompasses any and all embodiments within the scope of the following claims.
This application is a continuation-in-part of U.S. patent application Ser. No. 13/684,079, filed on Nov. 21, 2012.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 13684079 | Nov 2012 | US |
| Child | 14957476 | US |
