Method for preparing lignin-rich fiber for textile and composite materials through high-temperature directional degumming
A technology of lignin fibers and composite materials, which is applied in the field of high-temperature directional degumming to prepare lignin-rich fibers for textiles and composite materials. It can solve the problems of fiber disintegration and inability to achieve directional degumming, and achieve high bending strength.
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Embodiment 1
[0038] Dissolve sodium hydroxide in a certain amount of glycerin to form an alkali solution with a concentration of 8wt%. After soaking 10Kg of cotton stalk fiber in 40Kg of the above-mentioned alkali solution for 1min, centrifuge at 800r / min for about 2min to control the alkali solution and cotton The mass ratio of stalk bark fiber is 2:1. Heated under 400W power for 30s, washed with 4% NaOH aqueous solution and water successively at room temperature. After freeze-drying, it is carded on a roller carding machine to form cotton stalk skin fibers with a fineness of 22 dtex and a strength of 3.2 cN / dtex. The properties of the yarns and composite materials developed with the above-mentioned cotton stalk fiber are shown in Table 1. It can be seen from Table 1 that the strength of the yarn obtained by blending cotton stalk fiber and cotton after high-temperature directional degumming is 120% higher than that obtained by high-temperature alkali-boiled straw fiber. The composite ma...
Embodiment 2
[0043] Dissolve sodium hydroxide in a certain amount of glycerin to form an alkali solution with a concentration of 8wt%. After soaking 10Kg of cotton stalk fiber in 40Kg of the above-mentioned alkali solution for 1min, centrifuge at 800r / min for about 2min to control the alkali solution and cotton The mass ratio of stalk bark fiber is 2:1. Heated at 240W for 50S, washed with 4% NaOH and water at room temperature. After freeze-drying, it is carded on a roller carding machine to form cotton stalk skin fibers with a fineness of 23 dtex and a strength of 3.1 cN / dtex. The properties of the yarns and composite materials developed with the above-mentioned cotton stalk fiber are shown in Table 2. It can be seen from Table 2 that the strength of the blended yarn obtained by blending cotton stalk sheath fibers after high-temperature directional degumming with cotton is 100% higher than that of cotton stalk sheath fibers after high-temperature alkali boiling. The cotton stalk skin fib...
Embodiment 3
[0048] Dissolve sodium hydroxide in a certain amount of glycerin to form an alkali solution with a concentration of 8wt%. After soaking 10Kg of cotton stalk fiber in 40Kg of the above-mentioned alkali solution for 1min, centrifuge at 800r / min for about 2min to control the alkali solution and cotton The mass ratio of stalk bark fiber is 2:1. Heat it for about 5 minutes under 80W power, and wash it with 4% NaOH and water at room temperature. After freeze-drying, it is carded on a roller carding machine to form cotton stalk skin fibers with a fineness of 23 dtex and a strength of 3.0 cN / dtex. The properties of the yarns and composite materials developed with the above-mentioned cotton stalk fiber are shown in Table 3. It can be seen from Table 3 that the strength of the blended yarn obtained by blending the cotton stalk fiber and cotton after high-temperature directional degumming is 130% higher than that of the blended yarn obtained by high-temperature alkali boiling. The comp...
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Abstract
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