2022
DOI: 10.1039/d2ra05668b
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Investigation on dyeing mechanism of modified cotton fiber

Abstract: In this investigation, the dyeing mechanism of cotton fibers was investigated through adsorption isotherm, adsorption thermodynamics, adsorption kinetics, activation energy, diffusion coefficient, half-dyeing time and process of fixation.

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Cited by 11 publications
(4 citation statements)
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“…As depicted in Figure 6a,b, the reactive dye successfully penetrated the interior of both the raw and modified cotton fibers. The sulfur content was measured at 10 points along the cross-sectional diameter of the fibers, 47 revealing a gradual decrease in the sulfur content from the outside to the inside of the fibers. However, the sulfur content of the modified cotton fibers was considerably higher than that of the raw cotton fibers, indicating a superior dye permeability in the modified cotton fibers.…”
Section: Zeta Potential Analysismentioning
confidence: 99%
“…As depicted in Figure 6a,b, the reactive dye successfully penetrated the interior of both the raw and modified cotton fibers. The sulfur content was measured at 10 points along the cross-sectional diameter of the fibers, 47 revealing a gradual decrease in the sulfur content from the outside to the inside of the fibers. However, the sulfur content of the modified cotton fibers was considerably higher than that of the raw cotton fibers, indicating a superior dye permeability in the modified cotton fibers.…”
Section: Zeta Potential Analysismentioning
confidence: 99%
“…Unlike the ultrafast decays at approximately nanoseconds for fluorescent proteins, traditional dyes, , and quantum dots, Ln 3+ NCs generally exhibit much longer lifetimes (μs–ms) and thus wider tunable range, especially for their NIR emissions. The long fluorescence lifetime of Ln 3+ NCs lowers the difficulty of data acquisition and makes it easier to filter out background signals during the imaging process. , However, the wider tunable range of lifetime is advantageous for encoding information in lifetime imaging, leading to a significant improvement in spatial resolution for fluorescence lifetime imaging. ,, …”
Section: Introductionmentioning
confidence: 99%
“…Especially, NIR photons have lower light absorption and scattering in biological tissues as compared to visible photons and, therefore, can achieve deeper penetration for in vivo applications like bioimaging and phototherapy. 5−7 Unlike the ultrafast decays at approximately nanoseconds for fluorescent proteins, 8 traditional dyes, 9,10 and quantum dots, 11 Ln 3+ NCs generally exhibit much longer lifetimes (μs−ms) and thus wider tunable range, especially for their NIR emissions. The long fluorescence lifetime of Ln 3+ NCs lowers the difficulty of data acquisition and makes it easier to filter out background signals during the imaging process.…”
Section: ■ Introductionmentioning
confidence: 99%
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