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Polymeric nanofibers chemical composition

The current material system for protective clothes usually adopts a multilayer composite structure. An activated carbon-based chemical vapor filtration medium, a nonwoven or woven fabric, and a cover top layer are often incorporated. There is an opportunity to improve the performance of this system through the incorporation of one or several layers of nonwoven polymeric nanofiber mats. The polymeric... [Pg.73]

Composites of PANI-NFs, synthesized using a rapid mixing method, with amines have recently been presented as novel materials for phosgene detection [472]. Chemiresistor sensors with nanofibrous PANI films as a sensitive layer, prepared by chemical oxidative polymerization of aniline on Si substrates, which were surface-modified by amino-silane self-assembled monolayers, showed sensitivity to very low concentration (0.5 ppm) of ammonia gas [297]. Ultrafast sensor responses to ammonia gas of the dispersed PANI-CSA nanorods [303] and patterned PANI nanobowl monolayers containing Au nanoparticles [473] have recently been demonstrated. The gas response of the PANI-NTs to a series of chemical vapors such as ammonia, hydrazine, and triethylamine was studied [319,323]. The results indicated that the PANI-NTs show superior performance as chemical sensors. Electrospun isolated PANI-CSA nanofiber sensors of various aliphatic alcohol vapors have been proven to be comparable to or faster than those prepared from PANI-NF mats [474]. An electrochemical method for the detection of ultratrace amount of 2,4,6-trinitrotoluene with synthetic copolypeptide-doped PANI-NFs has recently been reported [475]. PANI-NFs, prepared through the in situ oxidative polymerization method, were used for the detection of aromatic organic compounds [476]. [Pg.67]

Another study by Hong et al. also reports the preparation of conducting PANI/nylon-6 composites with high electrical conductivity and superior mechanical properties, such as flexibility and lightness [24]. PANI was chemically polymerized on the surface of the nylon-6 electrospun nanofiber webs. The electrical conductivity measurements showed that the conductivity of the PANI/nylon-6 composite electrospun fiber webs was superior to that of PANI/nylon-6 plain-weave fabrics because of the high surface area/volume ratios. The volume conductivities of the PANI/nylon-6 composite electrospun fiber webs increased from 0.5 to 1.5 S cm as the di sion time increased from 10 min to 4h because of the even distribution of PANI in the electrospun fiber webs. However, the surface conductivities of the PANI/nylon-6 composite electrospun fiber webs somewhat decreased from 0.22 to 0.14 S cm as the di sion time increased, probably because PANI was contaminated with aniline monomers, aniline oligomers, and some alkyl chains, which served as electrical resistants. [Pg.171]

Rakhi et al reported the conducting-polymers (polyaniline [PANI] and PPy)-coated carbon nanocoils (CNCs) as efficient binder-free electrode materials for supercapacitors for the first time, in which the CNCs acted as a perfect backbone for the uniform distribution of the conducting polymers in the composites [16]. Ihe SC and maximum storage energy per unit mass of the composites were found to be comparable to one of the best-reported values for polymer-coated MWNTs. Dumanli et al. prepared the chemically bonded carbon nanofibers (CNFs)-PPy composite via electro-polymerization of Py on CNFs [17]. It showed that the final capacitance values were highly dependent on the number of deposition cycles and deposition rates. The best result for the coiled CNF-PPy composite system was found to be 27.6 C/cm at six times cycling using 25 mV/s. [Pg.422]

The chemical polymerization of Py by CAN in PU solutions leads to the formation of PU/PPy composites. The composites were characterized by Fourier transform infrared spectrophotometry-attenuated total reflectance (FTIR-ATR], dynamic mechanical analysis (DMA], thermal gravimetric analysis (TGA], differential scanning calorimetry (DSC], X-ray photoelectron spectroscopy (XPS], and SEM measurements. The absorbances of the disordered H-bonded urethane carbonyl decrease with increasing Py concentration. The fraction of the hydrogen-bonded carbonyls is increased and the melting point increases with the increase of PPy content. These indicate the incorporation of PPy into PU may cause the complex due to the intermolecular interaction between the PPy and PU. SEM images of composite nanofibers show good distribution of the second component and the composite solution is proper to form conductive composite nanofibers. [Pg.230]

Polyaniline nanofibers are synthesized through a simple, non-templated method, based on a modification of the classic chemical oxidative polymerization of aniline that makes nanofibers of uniform diameters. These materials respond significantly better than conventional films. To make the polyaniline even better for sensor materials, the nanofibers are dispensed into water and are combined with metals salts into a composite material. These... [Pg.10]


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