Device for the electronic and electrochemical measurement of analyte concentrations in biological samples
US-2024219386-A1 · Jul 4, 2024 · US
US10036105B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10036105-B2 |
| Application number | US-201414912981-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 21, 2014 |
| Priority date | Aug 21, 2013 |
| Publication date | Jul 31, 2018 |
| Grant date | Jul 31, 2018 |
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Described herein are nanofibers and methods for making porous carbon nanofibers. The pores have of any suitable size or shape. The presence and/or ordering of the pores results in a high surface area and/or high specific surface area. Such carbon is useful in a number of applications where high surface area carbon is desirable.
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What is claimed is: 1. A process for producing a mesoporous carbon nanofiber, the process comprising: a. electrospinning a fluid stock to produce a nanofiber, the fluid stock comprising a first polymer component and a second polymer component, the electrospinning of the fluid stock being gas-assisted; and b. thermally treating the nanofiber to carbonize the first polymer component and remove the second polymer component, thereby producing a mesoporous carbon nanofiber having an average mesopore size between 5 nm and 50 nm, wherein mesopores have a diameter of 2 nm to 50 nm and wherein the pore area of the mesopores is about 50 m 2 /g to about 200 m 2 /g. 2. The process of claim 1 , wherein the mesoporous carbon nanofiber has an average mesopore size of between 20 nm and 50 nm. 3. The process of claim 1 , wherein the weight ratio of first polymer to second polymer present in the fluid stock is 10:1 to 1:10. 4. The process of claim 3 , wherein the weight ratio of first polymer to second polymer present in the fluid stock is 10:1 to 1:4. 5. The process of claim 1 , wherein thermally treating the nanofiber comprises thermally treating the nanofiber at a temperature of at least 500° C. 6. The process of claim 1 , wherein thermally treating the nanofiber comprises a first thermal treatment at a temperature between 50° C. and 500° C. for at least 20 minutes and a second thermal treatment at a temperature of at least 500° C. for at least 20 minutes. 7. The process of claim 1 , wherein the first polymer comprises a polyacrylonitrile (PAN), polyvinylacetate (PVA), polyvinylpyrrolidone (PVP), cellulose, or ultra-high molecular weight polyethylene (UHMWPE). 8. The process of claim 1 , wherein the second polymer comprises a polyethylene oxide (PEO), polyvinylacetate (PVA), cellulose acetate, cellulose diacetate (CDA), cellulose triacetate, cellulose, nafion, polyvinylpyrrolidone (PVP), acrylonitrile butadiene styrene (ABS), polycarbonate, polymethylmethacrylate (PMMA), polyethylene terephthalate (PET), nylon, or polyphenylene sulfide (PPS). 9. The process of claim 1 , wherein the first and second polymer components comprise polyacrylonitrile (PAN) and polyethylene oxide (PEO), polyacrylonitrile (PAN) and cellulose diacetate (CDA), polyacrylonitrile (PAN) and polyvinyl alcohol (PVA), polyacrylonitrile (PAN) and polymethylmethacrylate (PMMA), or polyacrylonitrile (PAN) and polyvinylpyrrolidone (PVP). 10. The process of claim 1 , wherein electrospinning is co-axially gas-assisted. 11. The process of claim 1 , further comprising compressing the nanofiber during the thermal treatment. 12. The process of claim 1 , wherein the pore area of micropores of the mesoporous carbon nanofiber is less than 100 m 2 /g. 13. A mesoporous carbon nanofiber having a mesoporous pore area of at least 50 m 2 /g and an average mesoporous pore size between 5 nm and 50 nm, wherein mesopores have a diameter of between 2 nm and 50 nm. 14. The mesoporous carbon nanofiber of claim 13 , wherein the average mesoporous pore size is between 20 nm and 50 nm. 15. The mesoporous carbon nanofiber of claim 14 , wherein the mesoporous carbon nanofiber has a microporous area of less than 100 m 2 /g. 16. The mesoporous carbon nanofiber of claim 14 , having a pore area of at least 250 m 2 /g.
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