Publications by authors named "Tarek A Elmaaty"

Dyeing natural fabrics using supercritical carbon dioxide is challenging, especially without essential color hues. This work demonstrated that two newly developed reactive disperse dyes with distinct colors and shades were generated, one of which featured from the anthraquinone family and the other yellow, containing a pyrazole moiety. These new dyes and their combinations were used to dye cotton fabric using supercritical carbon dioxide and the highest K/S values were achieved at 8.

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Dyeing using supercritical carbon dioxide (SC-CO) is carried out on the polypropylene (PP) nanocomposite fabrics with model disperse dye compared with their regular fabric at various dyeing temperatures and pressures. The results are compared with those obtained in aqueous dyeing method. The PP nanocompsite fabrics dyed in SC-CO medium exhibited higher colour strength (K/S) values compared with their PP regular fabric.

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Pine wood (PW) and beech wood (BW) are the most used wood in furniture and other applications owing to their unique characteristics and low machining cost. However, their biodegradability and varied moisture content limit their wider use and durability. Therefore, in this study, nanotechnology was used as a novel eco-friendly approach to enhance the durability, antimicrobial properties, and color of wood.

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This work aims to utilize selenium nanoparticles (Se-NPs) as a novel dyestuff, which endows wool fibers with an orange color because of their localized surface plasmon resonance. The color characteristics of dyed fibers were evaluated and analyzed. The color depth of the dyed fabrics under study was increased with the increase in Se content and dyeing temperature.

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A series of eight alkyl and aryl alpha-nitro ketones were prepared by the potassium dichromate oxidation of the corresponding nitro alcohols. Short reaction times allowed for the easy isolation of pure nitro ketones that are devoid of starting materials and/or other oxidation side products.

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[reaction: see text] Alpha-nitro ketones can be transformed selectively into trialkyl-substituted pyrazines via reaction with alpha-amino ketones using octyl viologen as an electron-transfer reagent. The new synthetic method, and the optimal reaction conditions that allow for the regiochemical control, are described.

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