2005
DOI: 10.1016/j.carbon.2005.06.006
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Preparation and characterization of silylated graphite oxide

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Cited by 105 publications
(43 citation statements)
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“…Recently, graphite oxide (GO), also called graphitic acid, attracts the attention of many researcher groups owing to its promising applications as an adsorbent, 1, 2 a component in composite materials with photochemical, conductive, electric or adsorptive properties, [3][4][5][6] or a precursor in the formation of graphene layers. [7][8][9] As an adsorbent, GO has been tested in the retention of NO, NO 2 and NH 3 .…”
Section: Introductionmentioning
confidence: 99%
“…Recently, graphite oxide (GO), also called graphitic acid, attracts the attention of many researcher groups owing to its promising applications as an adsorbent, 1, 2 a component in composite materials with photochemical, conductive, electric or adsorptive properties, [3][4][5][6] or a precursor in the formation of graphene layers. [7][8][9] As an adsorbent, GO has been tested in the retention of NO, NO 2 and NH 3 .…”
Section: Introductionmentioning
confidence: 99%
“…The composition of the resulting GO www.frontiersin.org was C 8 H 3.0 O 4.5 . GO was silylated as follows (Matsuo et al, 2004(Matsuo et al, , 2005. GO (100 mg) was mixed with n-butylamine [C 4 H 9 NH 2 , hereafter abbreviated as C 4 , 2 ml; 32 mol/GO unit (C 8 H 3.0 O 4.5 )] as an exfoliating reagent in a sealed glass vial under an Argon atmosphere and the resulting solution was sonicated for 15 min (VELVO-CLEAR, VS-150; 50 kHz, 150 W), then heated at 60°C for 1 h. Dry toluene (5 ml, water content <30 ppm) was added to this solution and the solution was again sonicated.…”
Section: Methodsmentioning
confidence: 99%
“…The obtained silylated GO samples were then silylated with C 1 Si in the same manner as described above for 1 day for 1-4 times. The composition of silylated GO was determined from the weight of residual SiO 2 after thermogravimetric analysis, assuming that 0.4 n-butylamine molecules per GO were included (Matsuo et al, 2005). The resulting silylating GO was heated at 500°C under dynamic vacuum.…”
Section: Methodsmentioning
confidence: 99%
“…[15] This oxidation procedure was repeated for five times, and the composition was 55.58% carbon, 2.66% hydrogen and 41.76% oxygen, based on the elemental analysis of hydrogen and carbon. The obtained GO was silylated by MPTS in a similar manner as reported by Matsuo et al [16] GO (100 mg) and butylamine (1 ml) were mixed in a sealed glass vial in the presence of dry toluene (10 ml). The mixture was sonicated and then heated at 60 • C under nitrogen.…”
Section: Methodsmentioning
confidence: 99%