Method for preparing urea formaldehyde fiber through copolymerization modification
A technology of copolymerization modification and fiber, which is applied in the direction of fiber chemical characteristics, single-component synthetic polymer rayon, textiles and papermaking, etc. It can solve the problems that there are no related reports on fiber application, and achieve simple and easy curing and crosslinking. The effect of fast spinning speed and mild reaction conditions
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Embodiment 1
[0021] In this embodiment, the method for preparing urea-formaldehyde fiber by copolymerization modification is as follows:
[0022] (1) Dissolve PVA in water to obtain 1wt% PVA aqueous solution, add urea, melamine and formaldehyde (the molar ratio is 1:0.01:0.7), then add sodium hydroxide aqueous solution, adjust the pH to 7.5, and react at 45℃ for 0.5 h; The mass ratio of PVA to urea is 1:0.2; then add hydrochloric acid to adjust the pH to 4.0, and react at 40°C for 0.1h;
[0023] (2) Add calcium hydroxide aqueous solution again, adjust the pH to 7.4, and then add paraformaldehyde (the ratio of urea to paraformaldehyde in step (1) is 1:0.3), react at 35°C for 0.4h, Obtain a modified urea-formaldehyde solution with an aldehyde content of 0.09%;
[0024] (3) The obtained spinning solution is wet-spinned using a saturated sodium sulfate aqueous solution with a weight content of 0.1% boric acid as a coagulation bath, and the winding speed is 10m / min at a temperature of 10°C to obtain ...
Embodiment 2
[0027] In this embodiment, the method for preparing urea-formaldehyde fiber by copolymerization modification is as follows:
[0028] (1) Dissolve PEG in water to obtain 30wt% PEG aqueous solution, add urea, aniline and paraformaldehyde (molar ratio 1:1:0.7), then add potassium hydroxide aqueous solution, adjust the pH value to 10.5, at 95℃ React for 8 hours; wherein the mass ratio of PEG to urea is 1:10; then add sulfuric acid to adjust the pH to 6.9, and react at 95°C for 7 hours;
[0029] (2) Add sodium hydroxide aqueous solution again, adjust the pH to 10.5, then add formaldehyde (the ratio of urea to formaldehyde in step (1) is 1:2), react at 95°C for 8 hours to obtain an aldehyde content of 0.08 % Modified urea-formaldehyde solution;
[0030] (3) The resulting spinning solution is wet-spinned, using a saturated sodium sulfate aqueous solution with a weight content of 5% boric acid as a coagulation bath, and the winding speed is 500m / min at a temperature of 60°C to obtain nascen...
Embodiment 3
[0033] In this embodiment, the method for preparing urea-formaldehyde fiber by copolymerization modification is as follows:
[0034] (1) Dissolve polyvinyl formal in water to obtain 20wt% polyvinyl formal aqueous solution, add urea, phenol and glutaraldehyde (the molar ratio is 1:0.01:4), then add triethanolamine to adjust the pH value To 8.5, react at 90°C for 3 hours; wherein the mass ratio of polyvinyl formal to urea is 1:5; then add phosphoric acid to adjust the pH to 5, and react at 85°C for 2 hours;
[0035] (2) Add potassium hydroxide aqueous solution again, adjust the pH to 8.5, then add acetaldehyde (the ratio of urea to acetaldehyde in step (1) is 1:0.5), react at 75°C for 4 hours to obtain the aldehyde content 0.1% modified urea-formaldehyde solution;
[0036] (3) The obtained spinning solution is wet-spinned using a saturated sodium sulfate aqueous solution with a weight content of 3% boric acid as a coagulation bath, and the winding speed is 300m / min at a temperature of...
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