Field of the Invention
[0001] The present invention relates to the technical field of textile articles, and particularly
to an organic silicon-nitrogen flame-retardant regenerated cellulose fiber.
Background of the Invention
[0002] At present, more than 60% fire accidents in the globe are caused by textile articles,
and more than 80% casualty from fire accidents are caused by inhaling toxic smoke
or suffocation. As human civilization develops and countries promulgate anti-fire
security laws and regulations, people raise higher and higher requirements for flame-retardant
materials. The requirements change from pure consideration of flame-retardant performance
of materials to environment-friendliness, health care, appearance and comfort of flame-retardant
materials. Although flame-retardant synthetic fibers (flame-retardant polyester fiber,
flame-retardant acrylic fiber and the like) and intrinsically flame-retardant fibers
(aramid fiber, polyimide and the like) have excellent flame-retardant performance,
they have already failed to satisfy people's requirements for comfort and security
of clothes and accessories because of undesirable comfort of fiber fabric and drawbacks
such as shrinking, melting and drippage when catching on fire.
[0003] Flame-retardant regenerated cellulose fibers (e.g., flame-retardant viscose fiber)
currently available in the market may satisfy requirements for flame-retardant clothes
and accessories and people's requirements for fundamental comfort (moisture absorption
and air permeation) of dresses, they still have drawbacks to different degrees. For
example, phosphorous flame-retardant viscose fibers generate a lot of harmful fume
upon burning, phosphorous element is contained in fibers and fabric, the harmful fume
generated upon burning is prone to suffocate people, and their waste cause adverse
effects such as eutrophicating water resource during degradation; silicon-containing
flame-retardant viscose fibers have defects such as less strength and failure to ensure
alkali washing, can only be used as a non-woven fabric or filler, and cannot be used
as a shell fabric.
[0004] As compared with the above flame-retardant regenerated cellulose fibers, silicon-nitrogen-containing
flame-retardant regenerated cellulose fibers employ silicon-nitrogen-containing flame
retardant agent, overcome drawbacks such as large harmful fume emission of phosphorus-containing
flame-retardant viscose fibers and undesirable strength and non-endurance of alkali
washing of silicon-containing flame-retardant viscose fibers, can obtain products
with high flame-retardant performance and high textile performance, and are flame-retardant
regenerated cellulose fibers with promising development prospect. For example, patent
applications
CN103789858 and
CN104032401 publish silicon-nitrogen flame-retardant viscose fibers.
[0005] However, as the market raises increasing demands for performance of flame-retardant
regenerated cellulose fiber products, the current silicon-nitrogen containing flame-retardant
regenerated cellulose fibers are not be further improved in performance such as flame
retarding. Therefore, it is desirable to provide a silicon-nitrogen containing flame-retardant
regenerated cellulose fiber with better performance.
Summary of the Invention
[0006] The present invention provides an organic silicon-nitrogen flame-retardant regenerated
cellulose fiber. It is surprisingly found that introducing a certain proportion of
titanium (Ti) and calcium (Ca) simultaneously into the organic silicon-nitrogen flame-retardant
regenerated cellulose fiber can effectively improve the fiber flame-retarding performance
and substantively improve far infrared performance of the fiber without causing loss
of mechanics performance of the fiber.
[0007] The organic silicon-nitrogen flame-retardant regenerated cellulose fiber according
to the present invention includes silicon 5-15wt%, nitrogen 0.1-5wt%, oxygen 30-60wt%,
carbon 20-40wt%, hydrogen 1-7wt%, titanium 1-7wt% and calcium 1-7wt%.
[0008] Preferably, the organic silicon-nitrogen flame-retardant regenerated cellulose fiber
according to the present invention includes silicon 8.5-12.1wt%, nitrogen 1.0-2.3wt%,
oxygen 45-49.1wt%, carbon 28-31.5wt%, hydrogen 2.5-4.3wt%, titanium 3.5-4.6wt% and
calcium 1.9-3.4wt%.
[0009] The organic silicon-nitrogen flame-retardant regenerated cellulose fiber is formed
by allowing cellulose solution and organic silicon-nitrogen flame retardant to undergo
grating reaction, and then spinning, coagulating and regenerating. Specifically, the
flame retardant is added to the cellulose solution (e.g., viscose original liquid)
in a form of a hydrolytic dispersion liquid of silane. In the organic silicon-nitrogen
flame-retardant regenerated cellulose fiber, the flame-retarding component exists
in the fiber mainly in the form of oxides of silicon and amide, and additionally,
in the form of a small amount of oxides of titanium and oxides of calcium, and furthermore,
the flame-retarding component forms a crossing network with a linear regenerated cellulose
in a "T-shaped" structure. A total content of SiO
2, TiO
2 and CaO in the flame retardant is 12.3-57wt%, and content of amide is 6.5-30wt%,
wherein a ratio of silicon, titanium and calcium (mole ratio) is 1-10:1-5:1-23. The
silicon, titanium and calcium in the flame retardant are combined on a regenerated
cellulose main chain, form a silicon-titanium-calcium ceramic network, and constitute
a far infrared emission group.
[0010] A chemical formula of the organic silane hydrolytic dispersion liquid is:
[Me
xO
y·n SiO
2] + [--CONH]
Wherein Me represents metal ion; and the metal ion is Ti
4+ and Ca
2+.
[0011] The organic silicon-nitrogen flame-retardant regenerated cellulose fiber may also
be formed by injecting other additive such as colorant, antimicrobial agent, antistatic
agent before spinning to satisfy different demands of use.
[0012] The present invention further provides a method of preparing the organic silicon-nitrogen
flame-retardant regenerated cellulose fiber. The method comprises the following steps:
cellulose solution→blending with the organic silicon-nitrogen flame retardant→spinning→water
wash→drying. Furthermore, the method comprises the following steps: cellulose solution→blending
with the organic silicon-nitrogen flame retardant→spinning→water wash→fixing and cross-linking→water
wash→drying. Furthermore, the method comprises the following steps: cellulose solution→blending
with the organic silicon-nitrogen flame retardant→spinning→water wash→fixing and cross-linking
→ water wash → oiling → drying. The process of adding the flame retardant is: in the
above blending step, sufficiently blending the flame retardant and pre-formulated
cellulose solution, and the amount of addition of the flame retardant is 25-50%(w/w)
of cellulose content. The cellulose solution is preferably viscose original liquid.
[0013] Preferably, the process of preparing the organic silicon-nitrogen flame-retardant
regenerated cellulose fiber is:
- 1) Preparing viscose original liquid, sufficiently blending the organic silicon-nitrogen
flame retardant and pre-formulated viscose original liquid, the amount of addition
of the organic silicon-nitrogen flame retardant is 25-50%(w/w) of cellulose content
in the viscose original liquid, fabricating spinning adhesive, and then spinning and
water washing;
- 2) Performing fixing and cross-linking bath treatment for fibers after spinning and
water washing.
- 3) Performing oiling treatment for the fibers having undergone the fixing and cross-linking
bath treatment, and drying them.
[0014] Preferably, raw materials of the fixing and cross-linking agent employed by the fixing
and cross-linking bath comprise components such as polyhydroxy carboxylic acid, polyhroxy
alcohol, sugar and metal. The polyhdroxy carboxylic acid is one of or a mixture of
more of lactic acid, tartaric acid, citric acid or β -hydroxybutyric acid; the poyhdroxy
alcohol is one of or a mixture of more of propylene glycol, glycerol, glycol or polyhydroxy
sterol, and preferably uses C
6 polyhdroxy alcohol. The sugar is one of or a mixture of more of sucrose, fructose
or glucose. The metal component is one or a mixture of more of titanium tetrachloride,
calcium chloride, aluminum sulfate or four isopropyl titanate. The content of the
fixing and cross-linking agent is 3-6wt%.
[0015] The organic silicon-nitrogen flame-retardant regenerated cellulose fiber according
to the present invention may include other added components such as colorant, antimicrobial
agent, antistatic agent. During production, the above different components are added
to produce the organic silicon-nitrogen flame-retardant colored regenerated cellulose
fiber, organic silicon-nitrogen flame-retardant antimicrobial regenerated cellulose
fiber, and organic silicon-nitrogen flame-retardant antistatic regenerated cellulose
fiber.
[0016] The organic silicon-nitrogen flame-retardant regenerated cellulose fiber may be purely
spun into a yarn, fabric and shell fabric, and may also be spun with other fibers
or raw materials into blended fibers, for example, spun with multiple fibers such
as phosphorous-containing flame retardant regenerated cellulose fiber, silicon-containing
flame-retardant regenerated cellulose fiber, pure cotton, flame-retardant cotton,
various regenerated cellulose fibers (e.g., ordinary viscose fiber, modal fiber and
Tencel), wool, cashmere, aramid fiber, psa, polyimide, alginate fiber, various synthetic
fibers, various flame-retardant synthetic fibers, pre-oxidized fiber and glass fiber
in proportions, to produce yarns, fabrics and shell fabrics with different functions.
[0017] The organic silicon-nitrogen flame-retardant regenerated cellulose fiber or blended
fiber according to the present invention may also exist in the form of cellophane,
and then may be used as a high-rate decoration material or packaging material.
[0018] The organic silicon-nitrogen flame-retardant regenerated cellulose fiber or blended
fiber according to the present invention may also exist in the form of foam and may
be used as various flame-retardant filters such as flame-retardant mattress, flame-retardant
cushion or the like.
[0019] The organic silicon-nitrogen flame-retardant regenerated cellulose fiber or blended
fiber according to the present invention may also be used for protective clothing,
the wounded and patients' garments, the elderly's garment, infant and kid's garment,
interior decoration of marine, land and air transport vehicles, seat covers of public
places, sofa, mattress and curtain, close-fitting underwear, socks, joint protective
sheath (kneecap, elbow pad and wrist pad), bedding articles, garments and the like.
[0020] The oxygen index of the fabric made of organic silicon-nitrogen flame-retardant regenerated
cellulose fiber according to the present invention reaches 33-40%, and the fabric
is resistant to high temperature and washing with dilute soda-containing water, and
satisfies requirements of burning performance test of GB/5455-85
Textile Fabric Flame-retarding Performance Testing, and Perpendicular Method.
[0021] In addition, the organic silicon-nitrogen flame-retardant regenerated cellulose fiber
according to the present invention not only maintains the comfort (moisture absorption
and air permeation) of natural cellulose fibers, but also exhibits a far infrared
normal emission rate up to about 87%, may promotes human body blood circulation and
metabolism, and has a health care function of relieving fatigue, restoring strength,
and easing pain symptoms.
Detailed Description of Preferred Embodiments
Example 1
[0022] Pouring organic silicon-nitrogen flame retardant which accounts for 30wt% of the
amount of cellulose fibers into duly-formulated viscose original liquid, allowing
viscose to react with the flame retardant for 30 minutes, blending viscosity 70 seconds,
with a degree of ripeness (10% ammonium chloride) 10ml. using a spinning nozzle to
spin to regenerate in a coagulating bath, the coagulating bath including components:
sulphuric acid 75g/l, sodium sulphate 160g/l and zinc sulphate 20g/l, and the temperature
being 40°C. The regenerated fiber bundles are drawn, cut, washed, fixed and cross-linked,
bleached, oiled, dried, and packaged. The conditions for fixing and cross-linking
are: fixing and cross-linking agent:pure water:sodium bisulfite (weight ratio)=33:66:1,
the treatment duration is 15-40 minutes and the treatment temperature is 75°C.
[0023] A total content of SiO
2, TiO
2 and CaO in the flame retardant is 18.7wt%, content of amide is 12.5wt%; a ratio of
silicon, titanium and calcium (mole ratio) is 5.4:2.7:7.0.
Example 2
[0024] Pouring organic silicon-nitrogen flame retardant which accounts for 33wt% of the
amount of cellulose fibers into duly-formulated viscose original liquid, allowing
viscose to react with the flame retardant for 50 minutes, blending viscosity 80 seconds,
with a degree of ripeness (10% ammonium chloride) 14ml. using a spinning nozzle to
spin to regenerate in a coagulating bath, the coagulating bath including components:
sulphuric acid 100g/l, sodium sulphate 180g/l and zinc sulphate 30g/l, and the temperature
being 40°C. The regenerated fiber bundles are drawn, cut, washed, fixed and cross-linked,
bleached, oiled, dried, and packaged. The conditions for fixing and cross-linking
are: fixing and cross-linking agent:pure water:sodium bisulfite (weight ratio)=33:66:1,
the treatment duration is 15-40 minutes and the treatment temperature is 75°C.
[0025] A total content of SiO
2, TiO
2 and CaO in the flame retardant is 23wt%, content of amide is 18.7wt%; a ratio of
silicon, titanium and calcium (mole ratio) is 6.7:3.5:9.2.
Example 3
[0026] Pouring organic silicon-nitrogen flame retardant which accounts for 35wt% of the
amount of cellulose fibers into duly-formulated viscose original liquid, allowing
viscose to react with the flame retardant for 60 minutes, blending viscosity 70 seconds,
with a degree of ripeness (10% ammonium chloride) 16ml. using a spinning nozzle to
spin to regenerate in a coagulating bath, the coagulating bath including components:
sulphuric acid 125g/l, sodium sulphate 280g/l and zinc sulphate 50g/l, and the temperature
being 45°C. The regenerated fiber bundles are drawn, cut, washed, fixed and cross-linked,
bleached, oiled, dried, and packaged. The conditions for fixing and cross-linking
are: fixing and cross-linking agent:pure water:sodium bisulfite (weight ratio)=33:66:1,
the treatment duration is 15-40 minutes and the treatment temperature is 75°C.
[0027] A total content of SiO
2, TiO
2 and CaO in the flame retardant is 33wt%, content of amide is 28wt%; a ratio of silicon,
titanium and calcium (mole ratio) is 7.2:3.8:12.3.
Comparative example:
[0028] The flame-retardant viscose fiber is prepared according to the technical solution
of Example 2 of patent application
CN104032401B.
Performance test
[0029]
A. Dry breaking strength: tested by employing GB/T 14337 chemical fibers and by a
short fiber extension performance testing method;
B: Limiting oxygen index: tested by using FZ/T 50016 chemical fibers and using a viscose
short fiber flame-retarding performance testing method oxygen index method;
C: Burning performance: tested according to requirements of the GB/5455-85 standard;
D: Far infrared normal emission rate: tested by an experiment method of FZ/T 64010-2000.
[0030] Table 1 shows main quality data resulting from detecting the resultant organic silicon-nitrogen
flame-retardant regenerated cellulose fibers according to a detection method or relevant
standards. The dried fibers are spun into 32S yarns, and then the yarns are knitted
into 220g/m
2 shell fabric. Table 2 shows burning test data resulting from a burning performance
test according to the requirement of GB/T 5455-85 standard. Table 3 shows data of
detection of far infrared normal emission rate by a testing method of FZ/T 64010-2000.
Table 1: Comparison of main quality data
Nome of items |
Example 1 |
Example 2 |
Example 3 |
Comparative example |
Dry braking strength (CN/dtex) |
2.3 |
2.2 |
2.3 |
1.9 |
Limiting oxygen index (%) |
35.7 |
37.5 |
39.6 |
30.2 |
Table 2 : GB/ 5455-85 burning performance test data
Items |
Testing levels |
Example 1 |
Example 2 |
Example 3 |
Comparative example |
Level 1 |
Level 2 |
Level 3 |
Damage length/mm ≤ |
50 |
100 |
150 |
46 |
45 |
37 |
76 |
Afterflame duration/s ≤ |
0 |
4 |
8 |
0 |
0 |
0 |
2 |
Smolder duration/s ≤ |
0 |
4 |
8 |
0 |
0 |
0 |
4 |
Melting and dripping |
Not ignite absorbent cotton |
Not ignite absorbent cotton |
Not ignite absorbent cotton |
none |
none |
none |
none |
Table 3: FZ/T64010-2000 normal emission rate testing data
Normal emission rate standard of far infrared textile products |
Example 1 |
Example 2 |
Example 3 |
Comparative example |
≥83% |
87% |
88% |
89% |
80% |
Notes: 1. Ordinary cotton normal emission rate is 75%; 2. An improvement value of
a normal emission rate of far infrared textile products should be ≥8%. |
[0031] It can be seen from the above that the flame-retardant regenerated cellulose fiber
according to the present invention exhibits a higher limiting oxygen index, a better
flame-retarding performance and a far infrared function, and the normal emission rate
testing data reach the normal emission rate standard requirements of the textile article.
1. An organic silicon-nitrogen flame-retardant regenerated cellulose fiber, wherein the
organic silicon-nitrogen flame-retardant regenerated cellulose fiber includes silicon
5-15wt%, nitrogen 0.1-5wt%, oxygen 30-60wt%, carbon 20-40wt%, hydrogen 1-7wt%, titanium
1-7wt% and calcium 1-7wt%.
2. The organic silicon-nitrogen flame-retardant regenerated cellulose fiber according
to claim 1, wherein the flame-retardant components in the fiber exist in the form
of silicon oxides, titanium oxides, calcium oxides and amide structure.
3. The organic silicon-nitrogen flame-retardant regenerated cellulose fiber according
to claim 2, wherein the flame-retardant components exist in the form of SiO2, TiO2, CaO and amide structure, and a total content of SiO2, TiO2 and CaO in the flame retardant components is 12.3-57wt%, and content of amide is
6.5-30wt%,
4. The organic silicon-nitrogen flame-retardant regenerated cellulose fiber according
to claim 3, wherein a mole ratio of silicon, titanium and calcium is 1-10:1-5:1-23.
5. The organic silicon-nitrogen flame-retardant regenerated cellulose fiber according
to claim 2, wherein the flame-retardant components form a crossing network with a
linear regenerated cellulose in a "T-shaped" structure.
6. The organic silicon-nitrogen flame-retardant regenerated cellulose fiber according
to claim 2, wherein the flame-retardant components are added to a cellulose solution
in a form of an organic silane hydrolytic dispersion liquid as a flame retardant;
a chemical formula of the organic silane hydrolytic dispersion liquid is:
[MexOy·n SiO2] + [--CONH]
wherein Me represents metal ion; and the metal ion is Ti4+ and Ca2+.
7. The organic silicon-nitrogen flame-retardant regenerated cellulose fiber according
to claim 1, wherein the fiber further includes one or more additives selected from
a group consisting of colorant, antimicrobial agent and antistatic agent.
8. A method of preparing the organic silicon-nitrogen flame-retardant regenerated cellulose
fiber according to any one of claims 1-7, wherein the method comprises the following
steps: cellulose solution→blending with the organic silicon-nitrogen flame retardant→spinning→water
wash→drying; an amount of addition of the organic silicon-nitrogen flame retardant
is 25-50%(w/w) of cellulose content.
9. The method according to claim 8, wherein one or more additives selected from a group
consisting of colorant, antimicrobial agent and antistatic agent are added before
spinning.
10. A blended fiber comprising the organic silicon-nitrogen flame-retardant regenerated
cellulose fiber according to any one of claims 1-7, , and one or more of the following
fibers: phosphorous-containing flame retardant regenerated cellulose fiber, silicon-containing
flame-retardant regenerated cellulose fiber, pure cotton, flame-retardant cotton,
non-flame-retardant viscose fiber, modal fiber, Tencel, wool, cashmere, aramid fiber,
psa, polyimide, alginate fiber, synthetic fibers, flame-retardant synthetic fibers,
pre-oxidized fiber and glass fiber.