“…However, there are a few active groups on the AF surface and the amide functional group forms a p-conjugation effect on the adjacent benzene ring in the molecular chains. 4 At the same time, the ber possesses a smooth surface due to the high crystallinity and degree of orientation, 5 which all result in a poor interface combination between the ber and the matrix, especially the epoxy resin, seriously affecting the long-term and stable service of the composite materials. 6 In other words, the destruction of the AF-reinforced composite products during the service process is mainly attributed to the weak combination between the ber and the matrix.…”
In this article, the surface modification of AF with epichlorohydrin assisted by supercritical CO2 was investigated in order to improve the interface combination property between an aramid fiber and an epoxy resin matrix.
“…However, there are a few active groups on the AF surface and the amide functional group forms a p-conjugation effect on the adjacent benzene ring in the molecular chains. 4 At the same time, the ber possesses a smooth surface due to the high crystallinity and degree of orientation, 5 which all result in a poor interface combination between the ber and the matrix, especially the epoxy resin, seriously affecting the long-term and stable service of the composite materials. 6 In other words, the destruction of the AF-reinforced composite products during the service process is mainly attributed to the weak combination between the ber and the matrix.…”
In this article, the surface modification of AF with epichlorohydrin assisted by supercritical CO2 was investigated in order to improve the interface combination property between an aramid fiber and an epoxy resin matrix.
“…Furthermore, removal of carriers from inside the fibers is difficult. Extensive research has been conducted to overcome such drawbacks including the application of liquid ammonia, a pretreatment with amine solutions, supercritical carbon dioxide, and even surface modification with different techniques has been practiced, for example, diblock copolymer, UV light combined with ozone, and photografting . Such studies have obtained excellent results in improving dyeability of meta‐aramid fibers; however, another hurdle remains when applying those techniques.…”
Due to their high crystallinity and inertness, the coloration of meta-aramid fiber has been widely confirmed to be difficult. Though substantial improvements have been achieved, the dyeing of this fiber still requires high temperature and long duration for good color strength and shade. In this article, grafting poly(acrylic acid), a polyelectrolyte, onto meta-aramind fibers followed by dyeing via conventional pad-dry-cure technique resulted in good dyeing and a decrease the dyeing time and temperature. Dyed samples that possess industrially acceptable K/S values were produced in 15 minutes at room temperature (25-27 C) under neutral pH. Dyed samples had good dry and wet crockfastness.
“…11 Nevertheless, the carriers currently used always present high toxicity and bad smell, bringing in great inconvenience to the commercial Inspection for supercritical CO 2 dyeing of poly(m-phenylene isophthalamide) by kinetics and thermodynamics analysis production. 13 Furthermore, a huge amount of wastewater generated from the water dyeing procedure exacerbates concerns as high concentrations of unused dyes, surfactants, and other chemicals are contained. 14 Recently, supercritical carbon dioxide dyeing and finishing has already been investigated worldwide due to the distinct advantages of no water and recyclability of dyes, auxiliaries, and carbon dioxide.…”
Eco-friendly dyeing by using supercritical carbon dioxide as a medium has already been investigated worldwide due to the advantages of dyeing without water and recyclability of dyes and carbon dioxide. In this article, dyeing mechanism of poly(m-phenylene isophthalamide) was investigated in supercritical carbon dioxide. The obtained results showed that the dye uptake of Disperse Red 60 increased moderately with the temperature raising at constant pressure and achieved dyeing equilibrium after 70 min. By adding the carrier, diffusion coefficients of Disperse Red 60 in the polymer increased significantly in supercritical carbon dioxide. The activation energy for diffusion of Disperse Red 60 with and without carrier was 1165.91 and 1050.66 kJ mol−1, respectively. Moreover, the distribution coefficient, the standard affinity, the standard enthalpy, and the standard entropy of dyeing were also determined in supercritical carbon dioxide. These fundamental data are of vital importance on the green dyeing production of poly(m-phenylene isophthalamide).
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