POLYSACCHARIDE FIBERS AND METHOD FOR PRODUCING SAME
20180258557 · 2018-09-13
Inventors
- Gregor Kraft (A-4850 Timelkam, AT)
- Gert Kroner (A-4863 Seewalchen, AT)
- Thomas Röder (A-4840 Vöcklabruck, AT)
- Heinrich Firgo (A-4840 Vöcklabruck, AT)
Cpc classification
C08L5/00
CHEMISTRY; METALLURGY
D01F9/00
TEXTILES; PAPER
D21H13/00
TEXTILES; PAPER
C08B37/0009
CHEMISTRY; METALLURGY
International classification
C08L5/00
CHEMISTRY; METALLURGY
D21H13/00
TEXTILES; PAPER
D01F9/00
TEXTILES; PAPER
Abstract
The present invention relates to a method for the production of polysaccharide fibers which contain (1.fwdarw.3)-glucan as a fiber-forming substance, as well as to the fibers made thereby, and to their use.
Claims
1. A method for the production of a polysaccharide fiber whose fiber-forming substance is (1.fwdarw.3)-glucan, wherein the method is a modified viscose process.
2. The method according to claim 1, wherein at least 90% of the (1.fwdarw.3)-glucan are hexose units and at least 50% of the hexose units are linked via (1.fwdarw.3)-glycosidic bonds.
3. The method according to claim 1, wherein the fiber is a staple fiber or a continuous filament.
4. The method according to claim 1, wherein no more than 30% by weight of CS.sub.2, related to the fiber-forming substance, is used.
5. A polysaccharide fiber whose fiber-forming substance is (1.fwdarw.3)-glucan, wherein the polysaccharide fiber is produced using a modified viscose process.
6. The fiber according to claim 5, wherein at least 90% of the (1.fwdarw.3)-glucan are hexose units and at least 50% of the hexose units are linked via (1.fwdarw.3)-glycosidic bonds.
7. The fiber according to claim 5, wherein the fiber is a staple fiber or a continuous filament.
8. A textile product comprising the fiber according to claim 5, wherein the textile product is selected from the group consisting of yarns, woven fabrics, and knitted fabrics.
9. A product comprising the fiber according to claim 5, wherein the product is selected from the group consisting of nonwovens, hygiene articles, and of other, absorbent nonwoven products and papers.
10. The textile product according to claim 8, wherein the fiber is a staple fiber or a continuous filament.
11. The method according to claim 4, wherein less than 25% by weight of CS.sub.2, related to fiber-forming substance is used.
12. The method according to claim 11, wherein less than 15% by weight of CS.sub.2, related to fiber-forming substance is used.
13. The product according to claim 9, wherein the hygiene products are selected from the group consisting of tampons, panty liners and diapers.
14. The product according to claim 9, wherein the fiber is selected from the group consisting of a staple fiber and a continuous filament.
Description
EXAMPLES
[0036] The degree of polymerization of the (1.fwdarw.3)-glucans was determined by means of GPC in DMAc/LiCl. Subsequently, it is always the weight average of the degree of polymerization (DP.sub.w) that is specified.
Example 1
[0037] An aqueous glucan solution containing 9.1% of (1.fwdarw.3)-glucan with a DP.sub.W of 800 as well as 4.5% by weight of NaOH was reacted with 7.5% of CS.sub.2 (percent by weight calculated relative to the fiber-forming material). The viscose obtained in this way contained 9% by weight of fiber-forming material, 4.5% by weight of NaOH, and 0.57% by weight of sulfur. By using a spinneret, the solution was extruded into a regeneration bath containing 100 g/l of sulfuric acid, 330 g/l of sodium sulfate, and 35 g/l of zinc sulfate. The spinneret had 1053 perforations with a diameter of 50 m. 2.5% by weight of a nitrogen-containing auxiliary agent (Leomin AC80) were added to the viscose spinning solution. In order to achieve adequate fiber strength, stretching by approx. 75% was carried out in the second bath (92 C., 15 g/l of H.sub.2SO.sub.4). The draw-off velocity was 30 m/min.
[0038] The properties of the obtained fibers are listed in Table 1.
Example 2
[0039] An aqueous glucan solution containing 11% of (1.fwdarw.3)-glucan with a DP.sub.W of 1000 as well as 4.8% by weight of NaOH was reacted with 15% of CS.sub.2 (percent by weight calculated relative to the fiber-forming material). The viscose obtained in this way contained 10.8% by weight of fiber-forming material, 4.7% by weight of NaOH, and 1.37% by weight of sulfur. By using a spinneret, the solution was extruded into a regeneration bath containing 100 g/l of sulfuric acid, 330 g/l of sodium sulfate, and 45 g/l of zinc sulfate. The spinneret had 1053 perforations with a diameter of 50 m. 3% by weight of a nitrogen-containing auxiliary agent were added to the viscose spinning solution. In order to achieve adequate fiber strength, stretching by approx. 75% was carried out in the second bath (92 C., 15 g/l of H.sub.2SO.sub.4). The draw-off velocity was 25 m/min. The properties of the obtained fibers are listed in Table 1.
Example 3
[0040] An aqueous glucan solution containing 12.5% of (1.fwdarw.3)-glucan with a DP.sub.W of 800 as well as 4.4% by weight of NaOH was reacted with 12% of CS.sub.2 (percent by weight calculated relative to the fiber-forming material). The viscose obtained in this way contained 12.3% by weight of fiber-forming material, 4.3% by weight of NaOH, and 1.24% by weight of sulfur. By using a spinneret, the solution was extruded into a regeneration bath containing 90 g/l of sulfuric acid, 330 g/l of sodium sulfate, and 45 g/l of zinc sulfate. The spinneret had 1053 perforations with a diameter of 50 m. 1% by weight of a nitrogen-containing auxiliary agent was added to the viscose spinning solution. In order to achieve adequate fiber strength, stretching by approx. 75% was carried out in the second bath (92 C., 15 g/l of H.sub.2SO.sub.4). The draw-off velocity was 27 m/min. The properties of the obtained fibers are listed in Table 1.
TABLE-US-00001 TABLE 1 titer FFk FDk example dtex cN/tex % ex. 1 1.7 17.3 19.1 ex. 2 1.3 23.4 16.3 ex. 3 1.5 21.8 18.1 FFk fiber strength, conditioned FDk fiber elongation, conditioned