3-(Triethoxy silyl) propyl amine (TESPA) with different concentration 150, 75, and 25 wt.%
80°C
TEA
(i) Presence of amide in functionalized MWCNTs (ii) Modification of MWCNTs with respect to the pristine MWCNTs morphology (iii) The measurable mean diameter sizes of 25 wt.%, 75 wt.%, and 150 wt.% TESPA MWCNTs were 41.6, 49.2, and 80.38 nm
The effect of 3-(triethoxy silyl) propyl amine concentration on surface modification of multiwall carbon nanotubes
After reduction of functionalized CNT, the carbons attached to oxygenated groups did not return to the sp2 hybridization or restore a typical hexagonal graphitic structure No variation in the interlayer distance
Nanocatalysts derived from magnetic carbon nanotubes
Diameter distribution of CNT-amide was slightly decreased which was in the range of 10 to 109 nm, and the mean diameter was 32.16 nm with a standard deviation of 17.01 The functionalized CNTs are better aligned and denser because of the insertion of a new functional group
Effect of functionalized carbon nanotubes in the detection of benzene at room temperature
(i) Rough surface morphology because of the attachment of the alanine (ii) Larger diameter for the functionalized MWCNTs (mean diameter 84.80 nm) (iii) No agglomeration for functionalized MWCNTs (iv) Helix form of structure of functionalized MWCNTs
(i) The BET surface area 112.52 m2 g-1 containing both micro- and meso-porous structure (ii) Increased diameters as well as rougher, more corrugated surfaces (iii) Interlayer spacing of the modified MWCNTs was estimated to approximately 14 nm
(i) The diameter of the carbon nanotubes increased after grafting with folic acid molecules accompanied by the reducing aggregation of the carbon nanotubes
(i) The PEI loading was dependent on both total functional group loading and the surface area of CNT (ii) The maximum PEI loading could be obtained on CNT material with the highest total functional group loading (7.8 wt.%) and surface area (171.3 m2/g)