Modification method and dyeing process for salt-free low-alkaline deeply dyed type cellulose fiber fabric
A technology of cellulose fibers and fabrics, which is applied in the modification method of non-salt and low-alkali deep-dyed cellulose fiber fabrics and its dyeing process, which can solve the problems of poor dyeing depth, hardening, and colored flowers, and achieve enhanced adsorption , reduce the amount of usage, the effect of great function
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Embodiment 1
[0038] Embodiment 1: the preparation of chitosan oligosaccharide:
[0039] After the chitosan was completely dissolved with acetic acid solution, the catalyst MnO was added 2 / CuO, shake for 5min to 15min, then slowly add 30% (mass fraction) hydrogen peroxide, control the constant temperature at 60°C to carry out the degradation reaction in a shaking table water bath for 3h, adjust the pH of the degradation solution to neutral, and remove the hydrogen peroxide in the degradation product The metal ions are concentrated by vacuum rotary evaporation, precipitated with three times the volume of absolute ethanol, centrifuged to separate the chitosan oligosaccharide precipitate, and then dried in vacuum and ground into powder for use. Wherein the mass concentration fraction of chitosan in the degradation reaction is 3.5%, catalyst MnO 2 The mass concentration fraction of / CuO is 1.2%, the mass concentration fraction of 30% hydrogen peroxide is 4%, the consumption of acetic acid is ...
Embodiment 2
[0041] Embodiment 2: the preparation of chitosan oligosaccharide:
[0042] After the chitosan was completely dissolved with acetic acid solution, the catalyst MnO was added 2 / CuO, shake for 5min to 15min, then slowly add 30% (mass fraction) hydrogen peroxide, control the constant temperature at 50°C to carry out the degradation reaction in a shaking table water bath for 2h, adjust the pH of the degradation solution to neutral, and remove the hydrogen peroxide in the degradation product The metal ions are concentrated by vacuum rotary evaporation, precipitated with three times the volume of absolute ethanol, centrifuged to separate the chitosan oligosaccharide precipitate, and then dried in vacuum and ground into powder for use. Wherein the mass concentration fraction of chitosan in the degradation reaction is 3.5%, catalyst MnO 2 The mass concentration fraction of / CuO is 1.1%, the mass concentration fraction of 30% hydrogen peroxide is 3%, the consumption of acetic acid is ...
Embodiment 3
[0044] Embodiment 3: the preparation of chitosan oligosaccharide:
[0045] After the chitosan was completely dissolved with acetic acid solution, the catalyst MnO was added 2 / CuO, shake for 5min to 15min, then slowly add 30% (mass fraction) hydrogen peroxide, control the constant temperature at 50°C to carry out the degradation reaction in a shaking table water bath for 4h, adjust the pH of the degradation solution to neutral, and remove the hydrogen peroxide in the degradation product The metal ions are concentrated by vacuum rotary evaporation, precipitated with three times the volume of absolute ethanol, centrifuged to separate the chitosan oligosaccharide precipitate, and then dried in vacuum and ground into powder for use. Wherein the mass concentration fraction of chitosan in the degradation reaction is 3.5%, catalyst MnO 2 The mass concentration fraction of / CuO is 1%, the mass concentration fraction of 30% hydrogen peroxide is 5%, the consumption of acetic acid is 3%...
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