A process for the manufacture of a shaped body
US-2018305844-A1 · Oct 25, 2018 · US
US2016265144A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016265144-A1 |
| Application number | US-201415032660-A |
| Country | US |
| Kind code | A1 |
| Filing date | Oct 29, 2014 |
| Priority date | Oct 29, 2013 |
| Publication date | Sep 15, 2016 |
| Grant date | — |
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Disclosed is an activated carbon fiber, more specifically, a filament-type activated carbon fiber that is manufactured by activating a filament-type precursor fiber for the activated carbon fiber and has a strength of 0.01 to 1.0 g/denier so as to have improved durability.
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1 . A filament-type activated carbon fiber that is manufactured by activating a filament-type precursor fiber for the activated carbon fiber and has a strength of 0.01 to 1.0 g/denier. 2 . The filament-type activated carbon fiber of claim 1 , wherein the filament-type precursor fiber for the activated carbon fiber is selected from the group consisting of a cellulose-based filament-type precursor fiber, a polyacrylonitrile-based filament-type precursor fiber, and an aramid-based filament-type precursor fiber. 3 . The filament-type activated carbon fiber of claim 1 , wherein the filament-type precursor fiber has a strength of 5 to 12 g/denier. 4 . The filament-type activated carbon fiber of claim 1 , wherein the filament-type precursor fiber has a single-yarn fineness of 0.05 to 10 denier and a total fineness of 300 to 30,000 denier. 5 . A method of manufacturing an activated carbon fiber, the method comprising: (S1) stabilizing a filament-type precursor fiber; and (S2) activating the filament-type precursor fiber by carbonizing the stabilized filament-type precursor fiber in an inactive atmosphere. 6 . The method of claim 5 , further comprising: precipitating the filament-type precursor fiber in an alkali solution before step (S1). 7 . The method of claim 6 , wherein the filament-type precursor fiber is a cellulose-based filament-type precursor fiber or an aramid-based filament-type precursor fiber. 8 . The method of claim 5 , further comprising: drying the filament-type precursor fiber before step (S1). 9 . The method of claim 8 , further comprising: precipitating the filament-type precursor fiber in an alkali solution before the drying. 10 . The method of claim 8 , wherein the filament-type precursor fiber is a polyacrylonitrile-based filament-type precursor fiber. 11 . The method of claim 5 , wherein the stabilizing of step (S1) is performed using heat treatment in the inactive atmosphere at a temperature of 200 to 350° C. for 10 to 240 min when the filament-type precursor fiber is a cellulose-based filament-type precursor fiber or an aramid-based filament-type precursor fiber, and using heat treatment in ambient air at a temperature of 200 to 300° C. for 30 to 240 min when the filament-type precursor fiber is a polyacrylonitrile-based filament-type precursor fiber. 12 . The method of claim 5 , wherein the activating of step (S2) is performed at a temperature of 650 to 1,050° C. after low-temperature carbonization in the inactive atmosphere at a temperature of 300 to 500° C. for 1 to 30 min when the filament-type precursor fiber is a cellulose-based filament-type precursor fiber or an aramid-based filament-type precursor fiber, and at the temperature of 650 to 1,050° C. after high-temperature carbonization in the inactive atmosphere at a temperature of 500 to 950° C. for 1 to 30 min when the filament-type precursor fiber is a polyacrylonitrile-based filament-type precursor fiber. 13 . The method of claim 6 , wherein the alkali solution is selected from the group consisting of a phosphoric acid aqueous solution, an ammonium phosphate aqueous solution, and a zinc chloride aqueous solution. 14 . The method of claim 8 , wherein the drying is performed using heat treatment at a temperature of 100 to 150° C. 15 . A woven fabric manufactured using the activated carbon fiber of claim 1 . 16 . A knitted fabric manufactured using the activated carbon fiber of claim 1 . 17 . The method of claim 9 , wherein the alkali solution is selected from the group consisting of a phosphoric acid aqueous solution, an ammonium phosphate aqueous solution, and a zinc chloride aqueous solution.
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