Disclosure of Invention
In order to solve the problem that the flame retardant performance of the existing wool blended fabric is not strong, the application provides a high flame retardant wool blended fabric for automobile interiors.
The application provides a high flame retardant wool blended fabric for automotive interiors, which adopts the following technical scheme:
a high flame-retardant wool blended fabric for automotive interiors is woven by warp yarns and weft yarns;
the warp density is 150-250 pieces/10 cm; the weft yarn density is 140-240/10 cm;
the warp yarns are formed by blending polyester fibers, modified wool fibers and bamboo fibers; the weft yarns are formed by blending polyester fibers, modified wool fibers and carbon fibers;
the modified wool fiber is prepared from the following raw materials in parts by weight: 60-100 parts of wool fiber, 10-15 parts of dopamine hydrochloride, 3-5 parts of tris (hydroxymethyl) aminomethane, 20-30 parts of flame retardant, 8-12 parts of antistatic agent, 3-5 parts of penetrating agent, 20-50 parts of ethanol and 50-100 parts of water.
By adopting the technical scheme, the high-flame-retardance wool blended fabric for the automotive interior is composed of warp yarns and weft yarns, the density of the warp yarns and the weft yarns is controlled within a certain range, meanwhile, the warp yarns are formed by blending polyester fibers, modified wool fibers and bamboo fibers, and the weft yarns are formed by blending polyester fibers, modified wool fibers and carbon fibers; the polyester fiber has high strength, wear resistance and heat resistance; the bamboo fiber not only has excellent air permeability and water absorbability, stronger wear resistance and good dyeing property, but also has the characteristics of antibiosis, bacteriostasis, ultraviolet resistance, natural green environmental protection and the like; the carbon fiber has the advantages of light weight, high strength, high modulus, high temperature resistance, corrosion resistance and the like; the addition of the polyester fiber, the bamboo fiber and the carbon fiber ensures that the high-flame-retardance wool blended fabric for the automotive interior is excellent in mechanical property, good in chemical stability, antibacterial, wear-resistant and environment-friendly.
In addition, the application also adopts modified wool fibers, and raw materials for preparing the modified wool fibers comprise wool fibers, dopamine hydrochloride, tris (hydroxymethyl) aminomethane, a flame retardant, an antistatic agent, a penetrating agent and the like, so that the flame retardant property of the wool fibers can be remarkably improved, the antistatic property of the wool fibers is improved, the wool blended fabric has high flame retardant property, the comprehensive performance of the wool blended fabric is more excellent, and the wool blended fabric can be widely applied to the field of automotive interiors.
Preferably, the modified wool fiber is prepared by the following method:
s1, adding dopamine hydrochloride and tris (hydroxymethyl) aminomethane into ethanol, heating to 40-50 ℃, and adjusting the pH to 8.8-9.2 to obtain a dopamine-tris (hydroxymethyl) aminomethane solution; adding the wool fibers into the dopamine-tris (hydroxymethyl) aminomethane solution, stirring and reacting for a period of time, filtering and drying to obtain activated wool fibers;
s2, preparing a finishing liquid from a flame retardant, an antistatic agent, a penetrating agent, a dispersing agent and water, adding the activated wool fibers obtained in the step S1 into the finishing liquid, adjusting the pH to 3-4, treating at 70-80 ℃ for 40-60min, filtering, and drying to obtain the modified wool fibers.
By adopting the technical scheme, the dopamine hydrochloride and the tris (hydroxymethyl) aminomethane are adopted to form a dopamine-tris (hydroxymethyl) aminomethane solution, the dopamine-tris (hydroxymethyl) aminomethane solution is used for treating wool fibers, and a large number of active groups are generated on the surfaces of the wool fibers to obtain activated wool fibers; and then, a finishing liquid is formed by adopting a flame retardant and an antistatic agent, and the activated wool fibers are treated, so that the wool fibers are tightly combined with the flame retardant and the antistatic agent, and finally, the modified wool fibers have remarkable flame retardant property and good antistatic property, and have wide market prospect in the application of automobile interiors.
Preferably, the flame retardant is prepared by compounding tricarboxyethyl phosphine with the mass ratio of 2 (3-6) with phytic acid.
By adopting the technical scheme, the application adopts the compound of the tricarboxyethyl phosphine and the phytic acid as the flame retardant, and the compound ratio is controlled within a certain range; the tricarboxyethyl phosphine and the phytic acid are good flame retardants, can be stably combined with activated wool fibers through chemical bonds, and are synergistic, so that the flame retardant property of the modified wool fibers is greatly improved, and the aim of high flame retardance of the wool blended fabric is fulfilled; in addition, the tricarboxyethyl phosphine has different structures with the phytic acid molecules, so that the roughness of the surface of the wool fiber can be increased, the cohesion degree between the wool fibers is effectively improved, the tensile fracture performance of the modified wool fiber is enhanced, and the comprehensive performance of the modified wool fiber is obviously improved.
Preferably, the antistatic agent is prepared by mixing myristyl hydroxyethyl imidazoline with the mass ratio of (1-5) being 3 and nano copper.
Through adopting the technical scheme, the antistatic agent is prepared by mixing myristyl hydroxyethyl imidazoline and nano copper, and the organic antistatic agent and the inorganic antistatic agent are combined mutually and act together, so that the antistatic performance of the modified wool fiber is greatly improved.
Preferably, the penetrating agent is fatty alcohol polyoxyethylene ether and/or alkyl glycoside.
Through adopting above-mentioned technical scheme, the penetrating agent of this application is fatty alcohol polyoxyethylene ether and/or alkyl glycoside, can exert synergistic permeation and dispersion effect to a great extent, promotes each component in the finishing liquid and active wool fiber better effect, makes modified wool fiber's comprehensive properties more excellent.
Preferably, the wool fiber is treated as follows prior to modification:
firstly, adding wool fibers into 26-35% hydrogen peroxide by mass fraction, and pre-oxidizing for 25-35min at 42-48 ℃; adding the pre-oxidized wool fiber into complex enzyme, sodium gluconate and water, treating at 40-60deg.C for 30-90min, filtering, and drying to obtain pre-treated wool fiber.
Preferably, the pretreated modified wool is prepared by the following raw materials in parts by weight: 40-120 parts of wool fiber, 40-60 parts of hydrogen peroxide, 10-30 parts of complex enzyme, 6-10 parts of sodium gluconate and 30-50 parts of water.
By adopting the technical scheme, the method firstly uses hydrogen peroxide to perform pre-oxidation treatment on the wool fibers, removes long carbon chain lipoid on the wool surfaces, exposes the wool surface proteins, provides possibility for complex enzyme to attack the wool surface proteins, can open disulfide bonds in the wool proteins, and is favorable for the complex enzyme molecules to react with the wool fibers; then, in a weak alkaline environment, carrying out enzymolysis on the pre-oxidized wool fibers by adopting compound enzyme to obtain pre-treated wool fibers; the pretreatment method for the wool fibers has the advantages that the wool fibers are pretreated, the anti-felting performance of the wool fibers is effectively improved, the antistatic performance is improved, and the pretreated wool fibers can better interact with the dopamine-tris (hydroxymethyl) aminomethane solution, so that the flame retardant performance of the modified wool fibers is remarkably improved.
Preferably, the compound enzyme is prepared by compounding SZ protease and Savinase protease with the mass ratio of (3-7) to 4.
Through adopting above-mentioned technical scheme, the compound of this application adoption SZ protease and Savinase protease is as complex enzyme, and the two combined action can effectively get rid of the protein class impurity on wool surface, when improving the color and luster luminance of wool fibre, can also make the degradation effect of complex enzyme take place only in wool scale layer, plays the effect of protecting wool inner structure, reduction wool fibre damage for wool fibre better and dopamine-tris-hydroxymethyl aminomethane solution between interact.
Preferably, in the warp yarn, the mass ratio of the polyester fiber to the modified wool fiber to the bamboo fiber is (2-3): 3-4): 1; in the weft yarn, the mass ratio of the polyester fiber to the modified wool fiber to the carbon fiber is (5-6): (1-3): 2.
Through adopting above-mentioned technical scheme, the mass ratio between each fiber in this application control warp and the woof for each fiber gives play to self advantage better, makes wool blending fabric's fire behaviour more excellent, can apply to the automotive interior field better.
Preferably, the high-flame-retardance wool blended fabric for the automotive interiors is prepared by the following method:
mixing polyester fibers, modified wool fibers and bamboo fibers according to a mass ratio, and sequentially carrying out processes of slivering, drawing, gilling, compound gilling, combing, roving, spinning and spooling to obtain warp yarns;
mixing polyester fibers, modified wool fibers and carbon fibers according to a mass ratio, and sequentially carrying out processes of slivering, drawing, gilling, compound gilling, combing, roving, spinning and spooling to obtain weft yarns;
and weaving the warp yarn and the weft yarn by a rapier loom to obtain the high-flame-retardance wool blended fabric for the automobile interior trim.
By adopting the technical scheme, the method comprises the steps of firstly mixing the polyester fiber, the modified wool fiber and the bamboo fiber according to the mass ratio, sequentially carrying out processes of strip making, drawing, needle carding, compound needle carding, combing, roving, spinning and spooling to obtain warp yarns, and mixing the polyester fiber, the modified wool fiber and the carbon fiber according to the mass ratio by adopting the same operation to obtain weft yarns; the preparation method of the wool blended fabric is simple in steps and low in cost, is suitable for industrial production, and the obtained wool blended fabric has high flame retardant property and can be better applied to high performance requirements of automotive interior materials.
In summary, the present application has the following beneficial effects:
1. the high-flame-retardance wool blended fabric for the automotive interior trim is composed of warp yarns and weft yarns, wherein the warp yarns are formed by blending polyester fibers, modified wool fibers and bamboo fibers, and the weft yarns are formed by blending polyester fibers, modified wool fibers and carbon fibers; the wool blended fabric has excellent flame retardant property, mechanical property and antibacterial and antistatic properties, and has a wide application prospect in the field of automotive interiors.
2. The modified wool fiber is firstly activated by a dopamine-tris (hydroxymethyl) aminomethane solution, and then is finished by a finishing liquid containing a flame retardant and an antistatic agent, so that the modified wool fiber is obtained; the wool fiber is also pretreated, and is subjected to enzymolysis treatment by pre-oxidation and then complex enzyme; the prepared modified wool fiber has high flame retardant property and good antistatic function.
3. The high-flame-retardance wool blended fabric for the automotive interior has the advantages of simple preparation method and low preparation cost, is suitable for industrial production, has high flame retardance, and can be better applied to high performance requirements of automotive interior materials.
Detailed Description
The present application is described in further detail below with reference to examples.
Preparation examples 1-5, comparative preparation examples 1-5 provided pretreated wool fibers and methods of making the same.
Preparation example 1
Preparing pretreated modified wool, which comprises the following raw materials: 40kg of wool fiber, 40kg of hydrogen peroxide, 10kg of complex enzyme, 6kg of sodium gluconate and 30kg of water;
wherein the compound enzyme is prepared by compounding SZ protease and Savinase protease in a mass ratio of 3:4.
A pretreated wool fiber made by the process of:
firstly, adding wool fibers into 26% hydrogen peroxide by mass percent, and pre-oxidizing for 35min at 42 ℃; and adding the pre-oxidized wool fibers into the complex enzyme, sodium gluconate and water, treating at 40 ℃ for 90min, filtering and drying to obtain the pre-treated wool fibers.
Preparation example 2
Preparing pretreated modified wool, which comprises the following raw materials: 60kg of wool fibers, 45kg of hydrogen peroxide, 15kg of complex enzyme, 7kg of sodium gluconate and 35kg of water;
wherein the compound enzyme is prepared by compounding SZ protease and Savinase protease in a mass ratio of 1:1.
A pretreated wool fiber made by the process of:
firstly, adding wool fibers into 28% hydrogen peroxide by mass percent, and pre-oxidizing for 32min at 44 ℃; adding the pre-oxidized wool fibers into complex enzyme, sodium gluconate and water, treating at 45 ℃ for 75min, filtering and drying to obtain the pre-treated wool fibers.
Preparation example 3
Preparing pretreated modified wool, which comprises the following raw materials: 80kg of wool fibers, 50kg of hydrogen peroxide, 20kg of complex enzyme, 8kg of sodium gluconate and 40kg of water;
wherein the compound enzyme is prepared by compounding SZ protease and Savinase protease in a mass ratio of 5:4.
A pretreated wool fiber made by the process of:
firstly, adding wool fibers into 30% hydrogen peroxide by mass fraction, and pre-oxidizing for 30min at 46 ℃; and adding the pre-oxidized wool fibers into the complex enzyme, sodium gluconate and water, treating at 50 ℃ for 60min, filtering and drying to obtain the pre-treated wool fibers.
Preparation example 4
Preparing pretreated modified wool, which comprises the following raw materials: 100kg of wool fibers, 50kg of hydrogen peroxide, 20kg of complex enzyme, 9kg of sodium gluconate and 40kg of water;
wherein the compound enzyme is prepared by compounding SZ protease and Savinase protease in a mass ratio of 3:2.
A pretreated wool fiber made by the process of:
firstly, adding wool fibers into 32% hydrogen peroxide by mass fraction, and pre-oxidizing for 28min at 47 ℃; and adding the pre-oxidized wool fibers into the complex enzyme, sodium gluconate and water, treating at 55 ℃ for 45min, filtering and drying to obtain the pre-treated wool fibers.
Preparation example 5
Preparing pretreated modified wool, which comprises the following raw materials: 120kg of wool fiber, 60kg of hydrogen peroxide, 30kg of complex enzyme, 10kg of sodium gluconate and 50kg of water;
wherein the compound enzyme is prepared by compounding SZ protease and Savinase protease in a mass ratio of 7:4.
A pretreated wool fiber made by the process of:
firstly, adding wool fibers into 35% hydrogen peroxide by mass percent, and pre-oxidizing for 25min at 48 ℃; adding the pre-oxidized wool fibers into complex enzyme, sodium gluconate and water, treating at 60 ℃ for 30min, filtering and drying to obtain the pre-treated wool fibers.
Comparative preparation example 1
Comparative preparation 1, which differs from preparation 1 only in that: the complex enzyme was replaced with 4.3kg SZ protease.
Comparative preparation example 2
Comparative preparation 2, which differs from preparation 1 only in that: the complex enzyme was replaced with 5.7kg of Savinase protease.
Comparative preparation example 3
Comparative preparation 3, which differs from preparation 1 only in that: the pretreated wool fiber fabric is only pre-oxidized.
Comparative preparation example 4
Comparative preparation 4, which differs from preparation 1 only in that: the pretreated wool fibers were not pre-oxidized.
Comparative preparation example 5
Comparative preparation 5, which differs from preparation 1 only in that: sodium gluconate is not added.
Preparation examples 6-10, comparative preparation examples 6-18 provided modified wool fibers and methods of making the same.
Preparation example 6
Preparing modified wool fibers, which comprise the following raw materials: 60kg of pretreated wool fibers, 10kg of dopamine hydrochloride, 3kg of tris (hydroxymethyl) aminomethane, 20kg of flame retardant, 8kg of antistatic agent, 3kg of penetrating agent, 20kg of ethanol and 50kg of water;
wherein the pretreated wool fiber is preparation example 1; the flame retardant is prepared by compounding tricarboxyethyl phosphine and phytic acid in a mass ratio of 2:3; the antistatic agent is formed by mixing myristyl hydroxyethyl imidazoline and nano copper in a mass ratio of 1:3; the penetrating agent is prepared by mixing fatty alcohol polyoxyethylene ether and alkyl glycoside in a mass ratio of 1:1.
Modified wool fiber prepared by the following method:
s1, adding dopamine hydrochloride and tris (hydroxymethyl) aminomethane into ethanol, heating to 40 ℃, and adjusting the pH to 8.8 to obtain a dopamine-tris (hydroxymethyl) aminomethane solution; adding the pretreated wool fiber into a dopamine-tris (hydroxymethyl) aminomethane solution, stirring and reacting for 1.5h at the rotating speed of 600r/min at the temperature of 50 ℃, filtering and drying to obtain activated wool fiber;
s2, preparing a finishing liquid from a flame retardant, an antistatic agent, a penetrating agent, a dispersing agent and water, adding the activated wool fibers obtained in the step S1 into the finishing liquid, adjusting the pH value to 3, treating at 70 ℃ for 60min, filtering, and drying to obtain the modified wool fibers.
Preparation example 7
Preparing modified wool fibers, which comprise the following raw materials: 70kg of pretreated wool fibers, 12kg of dopamine hydrochloride, 3.5kg of tris (hydroxymethyl) aminomethane, 23kg of flame retardant, 9kg of antistatic agent, 3.5kg of penetrating agent, 25kg of ethanol and 60kg of water;
wherein the pretreated wool fiber is preparation example 2; the flame retardant is prepared by compounding tricarboxyethyl phosphine and phytic acid in a mass ratio of 1:2; the antistatic agent is formed by mixing myristyl hydroxyethyl imidazoline and nano copper in a mass ratio of 2:3; the penetrating agent is prepared by mixing fatty alcohol polyoxyethylene ether and alkyl glycoside in a mass ratio of 1:1.
Modified wool fiber prepared by the following method:
s1, adding ethanol into dopamine hydrochloride and tris (hydroxymethyl) aminomethane, heating to 42 ℃, and adjusting the pH value to 9 to obtain a dopamine-tris (hydroxymethyl) aminomethane solution; adding the pretreated wool fiber into a dopamine-tris (hydroxymethyl) aminomethane solution, stirring and reacting for 1.4 hours at the temperature of 52 ℃ and the rotating speed of 650r/min, filtering and drying to obtain activated wool fiber;
s2, preparing a finishing liquid from a flame retardant, an antistatic agent, a penetrating agent, a dispersing agent and water, adding the activated wool fibers obtained in the step S1 into the finishing liquid, adjusting the pH value to 3.2, treating at 72 ℃ for 55min, filtering, and drying to obtain the modified wool fibers.
Preparation example 8
Preparing modified wool fibers, which comprise the following raw materials: 80kg of pretreated wool fibers, 13kg of dopamine hydrochloride, 4kg of tris (hydroxymethyl) aminomethane, 25kg of flame retardant, 10kg of antistatic agent, 4kg of penetrating agent, 35kg of ethanol and 80kg of water;
wherein the pretreated wool fiber is preparation example 4; the flame retardant is prepared by compounding tricarboxyethyl phosphine and phytic acid in a mass ratio of 2:5; the antistatic agent is formed by mixing myristyl hydroxyethyl imidazoline and nano copper in a mass ratio of 1:1; the penetrating agent is prepared by mixing fatty alcohol polyoxyethylene ether and alkyl glycoside in a mass ratio of 1:1.
Modified wool fiber prepared by the following method:
s1, adding ethanol into dopamine hydrochloride and tris (hydroxymethyl) aminomethane, heating to 45 ℃, and adjusting the pH value to 9 to obtain a dopamine-tris (hydroxymethyl) aminomethane solution; adding the pretreated wool fiber into a dopamine-tris (hydroxymethyl) aminomethane solution, stirring and reacting for 1.3h at the temperature of 55 ℃ and the rotating speed of 700r/min, filtering and drying to obtain activated wool fiber;
s2, preparing a finishing liquid from a flame retardant, an antistatic agent, a penetrating agent, a dispersing agent and water, adding the activated wool fibers obtained in the step S1 into the finishing liquid, adjusting the pH value to 3.5, treating at 75 ℃ for 50min, filtering, and drying to obtain the modified wool fibers.
Preparation example 9
Preparing modified wool fibers, which comprise the following raw materials: 90kg of pretreated wool fibers, 14kg of dopamine hydrochloride, 4.5kg of tris (hydroxymethyl) aminomethane, 28kg of flame retardant, 11kg of antistatic agent, 4.5kg of penetrating agent, 45kg of ethanol and 90kg of water;
wherein the pretreated wool fiber is preparation example 4; the flame retardant is prepared by compounding tricarboxyethyl phosphine and phytic acid in a mass ratio of 4:11; the antistatic agent is formed by mixing myristyl hydroxyethyl imidazoline and nano copper in a mass ratio of 4:3; the penetrating agent is prepared by mixing fatty alcohol polyoxyethylene ether and alkyl glycoside in a mass ratio of 1:1.
Modified wool fiber prepared by the following method:
s1, adding ethanol into dopamine hydrochloride and tris (hydroxymethyl) aminomethane, heating to 48 ℃, and adjusting the pH to 9.1 to obtain a dopamine-tris (hydroxymethyl) aminomethane solution; adding the pretreated wool fiber into a dopamine-tris (hydroxymethyl) aminomethane solution, stirring and reacting for 1.2h at the temperature of 58 ℃ and the rotating speed of 750r/min, filtering and drying to obtain activated wool fiber;
s2, preparing a finishing liquid from a flame retardant, an antistatic agent, a penetrating agent, a dispersing agent and water, adding the activated wool fibers obtained in the step S1 into the finishing liquid, adjusting the pH value to 3.8, treating at 78 ℃ for 45min, filtering, and drying to obtain the modified wool fibers.
Preparation example 10
Preparing modified wool fibers, which comprise the following raw materials: 100kg of pretreated wool fibers, 15kg of dopamine hydrochloride, 5kg of tris (hydroxymethyl) aminomethane, 30kg of flame retardant, 12kg of antistatic agent, 5kg of penetrating agent, 50kg of ethanol and 100kg of water;
wherein the pretreated wool fiber is preparation 5; the flame retardant is prepared by compounding tricarboxyethyl phosphine and phytic acid in a mass ratio of 1:3; the antistatic agent is formed by mixing myristyl hydroxyethyl imidazoline and nano copper in a mass ratio of 5:3; the penetrating agent is prepared by mixing fatty alcohol polyoxyethylene ether and alkyl glycoside in a mass ratio of 1:1.
Modified wool fiber prepared by the following method:
s1, adding ethanol into dopamine hydrochloride and tris (hydroxymethyl) aminomethane, heating to 50 ℃, and adjusting the pH to 9.2 to obtain a dopamine-tris (hydroxymethyl) aminomethane solution; adding the pretreated wool fibers into a dopamine-tris (hydroxymethyl) aminomethane solution, stirring at 60 ℃ and a rotating speed of 800r/min for reaction for 1h, filtering, and drying to obtain activated wool fibers;
s2, preparing a finishing liquid from a flame retardant, an antistatic agent, a penetrating agent, a dispersing agent and water, adding the activated wool fibers obtained in the step S1 into the finishing liquid, adjusting the pH value to be 4, treating at 80 ℃ for 40min, filtering, and drying to obtain the modified wool fibers.
Comparative preparation example 6
Comparative preparation 6, which differs from preparation 6 only in that: the pretreated wool fiber was comparative preparation 1.
Comparative preparation example 7
Comparative preparation 7, which differs from preparation 6 only in that: the pretreated wool fiber was comparative preparation 2.
Comparative preparation example 8
Comparative preparation 8, which differs from preparation 6 only in that: the pretreated wool fiber was comparative preparation 3.
Comparative preparation example 9
Comparative preparation 9, which differs from preparation 6 only in that: the pretreated wool fiber was comparative preparation 4.
Comparative preparation example 10
Comparative preparation 10, which differs from preparation 6 only in that: the pretreated wool fiber was comparative preparation 5.
Comparative preparation 11
Comparative preparation 11, which differs from preparation 6 only in that: the pretreated wool fibers are replaced with non-pretreated wool fibers.
Comparative preparation example 12
Comparative preparation 12, which differs from preparation 6 only in that: the flame retardant was replaced by 8kg of tricarboxyethyl phosphine.
Comparative preparation example 13
Comparative preparation 13, which differs from preparation 6 only in that: the flame retardant was replaced with 12kg phytic acid.
Comparative preparation example 14
Comparative preparation 14, which differs from preparation 6 only in that: no flame retardant was added.
Comparative preparation example 15
Comparative preparation 15, which differs from preparation 6 only in that: the antistatic agent was replaced with 2kg of myristyl hydroxyethyl imidazoline.
Comparative preparation example 16
Comparative preparation 16, which differs from preparation 6 only in that: the antistatic agent was replaced with 6kg of nano copper.
Comparative preparation example 17
Comparative preparation 17, which differs from preparation 6 only in that: no antistatic agent was added.
Comparative preparation example 18
Comparative preparation 18, which differs from preparation 6 only in that: the pretreated wool fibers are not subjected to the activation treatment of step S1.
Examples 1-5 provide a high flame retardant wool blend fabric for automotive interiors.
Example 1
The high-flame-retardance wool blended fabric for the automotive interiors is prepared by the following method:
mixing 20kg of polyester fibers, 30kg of modified wool fibers and 10kg of bamboo fibers, and sequentially carrying out the procedures of slivering, drawing, needle carding, compound needle carding, combing, roving, spinning and spooling to obtain warps with the warp density of 150 warps/10 cm;
mixing 50kg of polyester fibers, 10kg of modified wool fibers and 20kg of carbon fibers, and sequentially performing processes of strip making, drawing, needle carding, compound needle carding, combing, roving, spinning and spooling to obtain weft yarns with the density of 140 weft yarns/10 cm;
weaving the warp yarn and the weft yarn by a rapier loom to obtain the high-flame-retardance wool blended fabric for the automotive interior trim;
wherein the modified wool fiber is preparation example 6.
Example 2
The high-flame-retardance wool blended fabric for the automotive interiors is prepared by the following method:
mixing 22kg of polyester fibers, 32kg of modified wool fibers and 10kg of bamboo fibers, and sequentially carrying out processes of slivering, drawing, needle carding, compound needle carding, combing, roving, spinning and spooling to obtain warps with the warp density of 180 yarns/10 cm;
mixing 52kg of polyester fibers, 15kg of modified wool fibers and 20kg of carbon fibers, and sequentially performing the processes of strip making, drawing, needle carding, compound needle carding, combing, roving, spinning and spooling to obtain weft yarns with the density of 170 yarns/10 cm;
weaving the warp yarn and the weft yarn by a rapier loom to obtain the high-flame-retardance wool blended fabric for the automotive interior trim;
wherein the modified wool fiber is preparation example 7.
Example 3
The high-flame-retardance wool blended fabric for the automotive interiors is prepared by the following method:
mixing 25kg of polyester fibers, 35kg of modified wool fibers and 10kg of bamboo fibers, and sequentially carrying out the procedures of slivering, drawing, needle carding, compound needle carding, combing, roving, spinning and spooling to obtain warps with the warp density of 200 warps/10 cm;
mixing 55kg of polyester fibers, 20kg of modified wool fibers and 20kg of carbon fibers, and sequentially performing the processes of strip making, drawing, needle carding, compound needle carding, combing, roving, spinning and spooling to obtain weft yarns with the density of 190 weft yarns/10 cm;
weaving the warp yarn and the weft yarn by a rapier loom to obtain the high-flame-retardance wool blended fabric for the automotive interior trim;
wherein the modified wool fiber is preparation example 8.
Example 4
The high-flame-retardance wool blended fabric for the automotive interiors is prepared by the following method:
mixing 28kg of polyester fibers, 38kg of modified wool fibers and 10kg of bamboo fibers, and sequentially carrying out the procedures of slivering, drawing, needle carding, compound needle carding, combing, roving, spinning and spooling to obtain warp with the density of 220 warps/10 cm;
mixing 58kg of polyester fibers, 25kg of modified wool fibers and 20kg of carbon fibers, and sequentially carrying out the processes of strip making, drawing, needle carding, compound needle carding, combing, roving, spinning and spooling to obtain weft yarns with the density of 210 yarns/10 cm;
weaving the warp yarn and the weft yarn by a rapier loom to obtain the high-flame-retardance wool blended fabric for the automotive interior trim;
wherein the modified wool fiber is preparation example 9.
Example 5
The high-flame-retardance wool blended fabric for the automotive interiors is prepared by the following method:
mixing 30kg of polyester fibers, 40kg of modified wool fibers and 10kg of bamboo fibers, and sequentially carrying out the procedures of slivering, drawing, needle carding, compound needle carding, combing, roving, spinning and spooling to obtain warps with the warp density of 250 warps/10 cm;
mixing 60kg of polyester fibers, 30kg of modified wool fibers and 20kg of carbon fibers, and sequentially performing processes of strip making, drawing, needle carding, compound needle carding, combing, roving, spinning and spooling to obtain weft yarns with the density of 240 weft yarns/10 cm;
weaving the warp yarn and the weft yarn by a rapier loom to obtain the high-flame-retardance wool blended fabric for the automotive interior trim;
wherein the modified wool fiber is preparation example 10.
To verify the performance of the highly flame retardant wool blend fabric for automotive interiors provided herein, applicants set comparative examples 1-14, wherein:
comparative example 1
Comparative example 1, which differs from example 1 only in that: the modified wool fiber was comparative preparation 6.
Comparative example 2
Comparative example 2, which differs from example 1 only in that: the modified wool fiber was comparative preparation 7.
Comparative example 3
Comparative example 3, which differs from example 1 only in that: the modified wool fiber was comparative preparation 8.
Comparative example 4
Comparative example 4, which differs from example 1 only in that: the modified wool fiber was comparative preparation 9.
Comparative example 5
Comparative example 5, which differs from example 1 only in that: the modified wool fiber was comparative preparation 10.
Comparative example 6
Comparative example 6, which differs from example 1 only in that: the modified wool fiber was comparative preparation 11.
Comparative example 7
Comparative example 7, which differs from example 1 only in that: the modified wool fiber was comparative preparation 12.
Comparative example 8
Comparative example 8, which differs from example 1 only in that: the modified wool fiber was comparative preparation 13.
Comparative example 9
Comparative example 9, which differs from example 1 only in that: the modified wool fiber was comparative preparation 14.
Comparative example 10
Comparative example 10, which differs from example 1 only in that: the modified wool fiber was comparative preparation 15.
Comparative example 11
Comparative example 11, which differs from example 1 only in that: the modified wool fiber was comparative preparation 16.
Comparative example 12
Comparative example 12, which differs from example 1 only in that: the modified wool fiber was comparative preparation 17.
Comparative example 13
Comparative example 13, which differs from example 1 only in that: the modified wool fiber was comparative preparation 18.
Comparative example 14
Comparative example 14, which differs from example 1 only in that: the modified wool fibers are replaced by unmodified wool fibers.
The main properties of the high flame retardant wool blended fabrics for automobile interiors in examples 1 to 5 and comparative examples 1 to 14 were respectively obtained to obtain the following result parameters, specifically shown in table 1:
the tensile breaking property of the high-flame-retardance wool blended fabric for the automotive interior is carried out by referring to GB/T3923-1997 method for measuring the breaking strength and the breaking elongation of the tensile property of fabrics;
the flame retardant property of the high flame retardant wool blended fabric for the automotive interior is tested by referring to GB/T5454-1997 oxygen index method for testing the combustion property of textiles and GB/T5455-1997 vertical method for testing the combustion property of textiles;
reference GB/T12703.2-2009, part 2 of the textile static test method: the charge surface density is used for testing the antistatic performance of the high-flame-retardance wool blended fabric for automobile interiors.
Table 1:
as can be seen from the data shown in table 1: the high-flame-retardance wool blended fabric for the automotive interiors in the embodiments 1-5 has the comprehensive performance far superior to that of the comparative examples 1-14, has the advantages of higher limiting oxygen index, V-0 vertical burning grade, higher tensile breaking strength and smaller charge surface density, has obvious flame retardance and excellent antistatic performance, and has wide application prospect in the automotive interiors field.
From example 1 and comparative examples 1 to 3, it is understood that: the modified wool fiber in the embodiment 1 is prepared in the preparation example 6, the wool fiber in the modified wool fiber is pretreated in the preparation example 1, the pre-oxidized wool fiber is subjected to enzymolysis by adopting a complex enzyme, the complex enzyme is prepared by compounding SZ protease and Savinase protease, and compared with the comparative examples 1-3, the flame retardant property and the antistatic property of the high flame retardant wool blended fabric for the automobile interior trim obtained in the embodiment 1 are better than those of the comparative examples 1-3, so that the wool fiber subjected to enzymolysis by the complex enzyme can be better combined with the dopamine-tris (hydroxymethyl) aminomethane solution.
As can be seen from example 1 and comparative example 4: the modified wool fiber of example 1 is prepared in preparation example 6, the wool fiber in the modified wool fiber is pretreated in preparation example 1, the wool fiber is pre-oxidized, and compared with comparative example 4, the high-flame-retardance wool blended fabric for automobile interior trim, which is obtained in example 1, has excellent flame retardance and simultaneously has correspondingly improved antistatic performance and mechanical property. As is clear from examples 1 and 5, the modified wool fiber of example 1 is prepared in preparation example 6, and the wool fiber in the modified wool fiber is pretreated in preparation example 1, and the enzymatic hydrolysis of the pre-oxidized wool fiber is more excellent in comprehensive performance than that of the high flame retardant wool blended fabric for automobile interior trim, which is obtained in example 1, in comparison with comparative example 5 under the condition of weak alkalinity of sodium gluconate.
As is clear from example 1 and comparative example 6, the modified wool fiber of example 1 is prepared in preparation example 6, and the wool fiber of the modified wool fiber is pretreated in preparation example 1, compared with comparative example 6, the high flame retardant wool blended fabric for automobile interior trim obtained in example 1 has remarkable flame retardant property and excellent mechanical property.
As can be seen from examples 1 and comparative examples 7 to 9, the modified wool fiber in example 1 is prepared from preparation example 6, and the flame retardant is prepared by compounding tricarboxyethyl phosphine and phytic acid, and compared with comparative examples 7 to 9, the flame retardant performance of the high flame retardant wool blended fabric for automobile interior trim obtained in example 1 is significantly enhanced.
As is clear from examples 1 and comparative examples 10 to 12, the modified wool fiber in example 1 was prepared from preparation example 6, and the antistatic agent was prepared by mixing myristyl hydroxyethyl imidazoline with nano copper, and it is clear that the antistatic property of the highly flame retardant wool blend fabric for automobile interior trim obtained in example 1 was more excellent than that of comparative examples 10 to 12.
As is clear from example 1 and comparative example 13, the modified wool fiber in example 1 was prepared in preparation example 6, and the pretreated wool fiber was subjected to the activation treatment in step S1, and compared with comparative example 13, the high flame retardant wool blend fabric for automobile interior trim obtained in example 1 was superior to comparative example 13 in mechanical properties, flame retardant properties and antistatic properties.
As can be seen from example 1 and comparative example 14, the modified wool fiber used in example 1 has a higher limiting oxygen index, a vertical combustion grade of V-0, a higher tensile breaking strength, a smaller charge surface density and a better overall performance than that of comparative example 14, and the wool blended fabric obtained in example 1 has a wide application prospect in the field of automotive interiors.
The present embodiment is merely illustrative of the present application and is not intended to be limiting, and those skilled in the art, after having read the present specification, may make modifications to the present embodiment without creative contribution as required, but is protected by patent laws within the scope of the claims of the present application.