1975
DOI: 10.1016/0008-6223(75)90005-6
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Low temperature electrochemical preparation of carbon with a high surface area from polytetrafluoroethylene

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Cited by 70 publications
(19 citation statements)
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“…chemical derivitization of PTFE surfaces. These anhydrous dichloromethane (DCM), octadecylacrylate, bromine, and ethyl alcohol (Et-OH) were methods include treatment with alkali metals in the presence of ammonia [2][3][4] and treatment with purchased from Aldrich (Milwaukee, WI). Sulfuric acid (95 to 98%) was purchased from EM Sciglow discharges, 5,6 especially with plasmas containing scavengers for fluorine radical to prevent ence (Gibbstown, NJ).…”
Section: Introductionmentioning
confidence: 99%
“…chemical derivitization of PTFE surfaces. These anhydrous dichloromethane (DCM), octadecylacrylate, bromine, and ethyl alcohol (Et-OH) were methods include treatment with alkali metals in the presence of ammonia [2][3][4] and treatment with purchased from Aldrich (Milwaukee, WI). Sulfuric acid (95 to 98%) was purchased from EM Sciglow discharges, 5,6 especially with plasmas containing scavengers for fluorine radical to prevent ence (Gibbstown, NJ).…”
Section: Introductionmentioning
confidence: 99%
“…25,26 The amount of carbon in the 2:1 sample was 16.7wt% measured by elemental analysis (CHNS E.A). From these understandings of the effects of PTFE and T on the synthesis of FeF 3 , we selected an optimized synthesis condition: 2:1 w:w PTFE: Fe(C 2 O 4 )•2H 2 O at 600°C for 1 h under Ar.…”
Section: Fe(c 2 O 4 )·2h 2 O → Fe(c 2 O 4 ) + Ptfe → Fe 3 O 4 + Cf 2 mentioning
confidence: 99%
“…Conversely, the precise control of the porosity will sometimes necessitate other more effective methods, such as those using the inorganic template materials [8]. A method similar to the template method, the defluorination of polytetrafluoroethylene(PTFE) by means of alkali metals, also may allow for the synthesis of amorphous porous carbons without the use of a conventional activation process at high temperature [8][9][10][11][12]. In this process, a sp 1 carbyne-like chain structure is temporarily formed at the first step of defluorination of PTFE [13] followed by partial cross-inking between the vicinal linear chains to lead to sp 2 carbon products such as by-products around the inorganic alkali fluoride particles; finally, the particles can be easily removed from the carbon matrix by acid treatment to produce pores in the carbon.…”
Section: Introductionmentioning
confidence: 99%