阅读说明：本技术 一种强耐磨性的防静电面料及其制备方法 (Antistatic fabric with high wear resistance and preparation method thereof ) 是由 罗欣玲 于 2021-09-16 设计创作，主要内容包括：本发明公开了一种强耐磨性的防静电面料及其制备方法,包括以下重量份原料：60-70份羊毛纤维、40-50份竹炭涤纶纤维、3-5份复合整理剂。该强耐磨性的防静电面料,通过使用复合整理剂对各个纤维进行高温整理,在高温的条件下,产物a中的疏水基团向疏水性纤维表面结合或靠近,而亲水性基团聚醚组分则向着空气一侧排列,在空气和纤维的界面形成了定向排列,亲水基团可以吸收空气中的水分,在纤维表面形成一层导电性较好的水膜,从而使织物的表面电荷逸散速率加快,降低纤维表面电阻,起到消除静电的作用,另外通过在复合整理剂中添加了脂肪长链,使聚酯链段与涤纶分子发生共熔共晶作用,有效提高面料的防静电效果。(The invention discloses a strong-wear-resistance anti-static fabric and a preparation method thereof, wherein the fabric comprises the following raw materials in parts by weight: 60-70 parts of wool fiber, 40-50 parts of bamboo charcoal polyester fiber and 3-5 parts of composite finishing agent. This antistatic fabric of strong wearability, carry out high temperature arrangement to each fibre through using compound finishing agent, under the condition of high temperature, hydrophobic group in the product a combines or is close to hydrophobic fibre surface, and hydrophilic group polyether component is arranged towards air one side, directional arrangement has been formed at the interface of air and fibre, hydrophilic group can absorb the moisture in the air, form the better water film of one deck electric conductivity on the fibre surface, thereby make the surface charge dissipation rate of fabric accelerate, reduce fibre surface resistance, play the effect of static elimination, in addition through having added the fat long chain in compound finishing agent, make polyester chain segment and dacron molecule take place eutectic effect of eutectic melting, effectively improve the antistatic effect of surface fabric.)

1. The utility model provides a strong wearability prevents static surface fabric which characterized in that: the feed comprises the following raw materials in parts by weight: 60-70 parts of wool fiber, 40-50 parts of bamboo charcoal polyester fiber and 3-5 parts of composite finishing agent;

the antistatic fabric with strong wear resistance is prepared by the following steps:

adding a composite finishing agent into purified water, adjusting the concentration of the composite finishing agent to be 12-13g/L, and then adjusting the pH value of the composite finishing agent to be 4-5 for later use;

pouring the treated composite finishing agent into a baking container, then carrying out pre-baking treatment on the wool fibers and the bamboo charcoal polyester fibers, then carrying out two-dipping and two-rolling treatment on the wool fibers and the bamboo charcoal polyester fibers in the composite finishing agent, setting the baking temperature at 140-155 ℃ and the baking time at 60-90s, and finishing the surface treatment on the wool fibers and the bamboo charcoal polyester fibers;

and step three, performing blending treatment on the wool fibers and the bamboo charcoal polyester fibers after surface treatment to obtain warp yarns and weft yarns, putting the warp yarns and the weft yarns into a singeing machine for singeing treatment, putting the warp yarns and the weft yarns into the slurry for soaking for 5-10min, pressing off the residual slurry, washing with clear water, naturally airing, and finally weaving the aired warp yarns and weft yarns to form the fabric, thereby obtaining the antistatic fabric with strong wear resistance.

2. The antistatic fabric with strong wear resistance as claimed in claim 1, wherein: in the second step, the pre-drying temperature of the wool fibers and the bamboo charcoal polyester fibers is 350 ℃.

3. The antistatic fabric with strong wear resistance as claimed in claim 1, wherein: the serous fluid is prepared from oxidized corn starch, ethylene glycol, sodium carboxymethyl cellulose, chitosan and water according to a mass ratio of 2: 1: 0.2: 0.2: 6.

4. The antistatic fabric with strong wear resistance as claimed in claim 1, wherein: the composite finishing agent is prepared by the following steps:

step A1, weighing dimethyl terephthalate, ethylene glycol and p-toluenesulfonic acid, mixing, heating the mixture until methanol in the mixture is completely distilled off, adding polyethylene glycol and a catalyst into the mixture, heating after introducing nitrogen, and distilling the mixture under reduced pressure to obtain a product a;

a2, weighing the product a, adding the product a into a beaker, adding water into the beaker, adding an emulsifier into the beaker, uniformly stirring, heating the beaker in a water bath, adding a long fat chain into the beaker while stirring, and uniformly stirring to obtain a product b;

step A3, adding the product b into deionized water for dilution, uniformly stirring for later use, weighing glacial acetic acid, adding the glacial acetic acid into the deionized water for dilution, and uniformly stirring for later use;

step A4, weighing secondary amino polysiloxane, low-yellowing amino polysiloxane X, octadecyl trimethyl ammonium chloride and dodecyl dimethyl betaine, putting into an emulsification tank together, controlling the emulsification tank to stir at the speed of 50-60r/min for 15-20min, uniformly mixing all the materials, heating in a water bath to 50 ℃, adding deionized water into the emulsification tank, setting the stirring speed at 180-200r/min, and carrying out stirring reaction for 40-60min to obtain a product c;

and A5, adding the diluted product b into the product c, setting the stirring speed to be 50-60r/min, stirring and reacting for 20-30min, controlling the temperature to be 25-30 ℃, finally adding diluted glacial acetic acid, and adjusting the pH value of the mixed solution to be 5.5 to obtain the composite finishing agent.

5. The antistatic fabric with strong wear resistance as claimed in claim 4, wherein: in the step A1, the mixing mass ratio of dimethyl terephthalate, ethylene glycol and p-toluenesulfonic acid is 1: 0.8: 0.8, the mass ratio of the polyethylene glycol to the catalyst is 1:0.3, the total mass of the polyethylene glycol and the catalyst is 12 percent of the total mass of the system, and the catalyst is antimony trioxide.

6. The antistatic fabric with strong wear resistance as claimed in claim 4, wherein: in step A2, the ratio of product a to water used was 10 g: 100mL, the emulsifier is OP-15, the dosage of the emulsifier is 2g/L, the temperature of water bath heating is 60 ℃, and the mass ratio of the fat long chain to the product a is 10: 3.

7. The antistatic fabric with strong wear resistance as claimed in claim 4, wherein: in step A3, the mixing mass ratio of the product b and deionized water was 1.5:1, and the mixing mass ratio of glacial acetic acid and deionized water was 1: 3.

8. The antistatic fabric with strong wear resistance as claimed in claim 4, wherein: in the step A4, the mass ratio of the secondary amino polysiloxane, the low-yellowing amino polysiloxane X, the octadecyl trimethyl ammonium chloride and the dodecyl dimethyl betaine is 1:2:2:1.5, and the dosage of the deionized water is twice of the total mass of the system.

9. A preparation method of an antistatic fabric with strong wear resistance is characterized by comprising the following steps: the method comprises the following steps:

adding a composite finishing agent into purified water, adjusting the concentration of the composite finishing agent to be 12-13g/L, and then adjusting the pH value of the composite finishing agent to be 4-5 for later use;

pouring the treated composite finishing agent into a baking container, then carrying out pre-baking treatment on the wool fibers and the bamboo charcoal polyester fibers, then carrying out two-dipping and two-rolling treatment on the wool fibers and the bamboo charcoal polyester fibers in the composite finishing agent, setting the baking temperature at 140-155 ℃ and the baking time at 60-90s, and finishing the surface treatment on the wool fibers and the bamboo charcoal polyester fibers;

and step three, performing blending treatment on the wool fibers and the bamboo charcoal polyester fibers after surface treatment to obtain warp yarns and weft yarns, putting the warp yarns and the weft yarns into a singeing machine for singeing treatment, putting the warp yarns and the weft yarns into the slurry for soaking for 5-10min, pressing off the residual slurry, washing with clear water, naturally airing, and finally weaving the aired warp yarns and weft yarns to form the fabric, thereby obtaining the antistatic fabric with strong wear resistance.

Technical Field

The invention relates to the technical field of fabrics, in particular to an anti-static fabric with high wear resistance and a preparation method thereof.

Background

Fabric is the material used to make clothing. As one of the three elements of the clothes, the fabric can not only explain the style and the characteristics of the clothes, but also directly control the expression effects of the color and the shape of the clothes, and common clothes fabrics comprise cotton cloth, linen, silk, wool, chemical fiber, blended fabric and modal.

In the process of mutual friction of different fabrics, static charges are generated on the surface of the fabric, especially for various acrylic fabrics, when clothes made of the fabric are taken off and worn, the fabric rubs with inner-layer clothes, high-voltage charges are easily generated, air between the inner-layer clothes and the outer-layer clothes is punctured, static electricity is formed, the static electricity can have greater frightening performance and harmfulness to old people and children, currently, antistatic agent PEE is usually used for finishing the fabric to enable the fabric to have better antistatic performance and durability, but the fabric finished by the antistatic agent PEE has reduced hand feeling, the comfort of the fabric is reduced, and in order to solve the problems, technical personnel in the field provide the antistatic fabric with strong wear resistance and the preparation method thereof.

Disclosure of Invention

Technical problem to be solved

Aiming at the defects of the prior art, the invention provides the anti-static fabric with strong wear resistance and the preparation method thereof, and solves the problems that the hand feeling of the fabric finished by the antistatic agent PEE is reduced and the comfort of the fabric is reduced.

(II) technical scheme

In order to achieve the purpose, the invention is realized by the following technical scheme: the antistatic fabric with high wear resistance comprises the following raw materials in parts by weight: 60-70 parts of wool fiber, 40-50 parts of bamboo charcoal polyester fiber and 3-5 parts of composite finishing agent;

the antistatic fabric with strong wear resistance is prepared by the following steps:

adding a composite finishing agent into purified water, adjusting the concentration of the composite finishing agent to be 12-13g/L, and then adjusting the pH value of the composite finishing agent to be 4-5 for later use;

pouring the treated composite finishing agent into a baking container, then carrying out pre-baking treatment on the wool fibers and the bamboo charcoal polyester fibers, then carrying out two-dipping and two-rolling treatment on the wool fibers and the bamboo charcoal polyester fibers in the composite finishing agent, setting the baking temperature at 140-155 ℃ and the baking time at 60-90s, and finishing the surface treatment on the wool fibers and the bamboo charcoal polyester fibers;

and step three, performing blending treatment on the wool fibers and the bamboo charcoal polyester fibers after surface treatment to obtain warp yarns and weft yarns, putting the warp yarns and the weft yarns into a singeing machine for singeing treatment, putting the warp yarns and the weft yarns into the slurry for soaking for 5-10min, pressing off the residual slurry, washing with clear water, naturally airing, and finally weaving the aired warp yarns and weft yarns to form the fabric, thereby obtaining the antistatic fabric with strong wear resistance.

Preferably, in the second step, the pre-drying temperature of the wool fibers and the bamboo charcoal polyester fibers is 350 ℃.

Preferably, the slurry is prepared from oxidized corn starch, ethylene glycol, sodium carboxymethyl cellulose, chitosan and water according to a mass ratio of 2: 1: 0.2: 0.2: 6.

Preferably, the composite finishing agent is prepared by the following steps:

step A1, weighing dimethyl terephthalate, ethylene glycol and p-toluenesulfonic acid, mixing, heating the mixture until methanol in the mixture is completely distilled off, adding polyethylene glycol and a catalyst into the mixture, heating after introducing nitrogen, and distilling the mixture under reduced pressure to obtain a product a;

a2, weighing the product a, adding the product a into a beaker, adding water into the beaker, adding an emulsifier into the beaker, uniformly stirring, heating the beaker in a water bath, adding a long fat chain into the beaker while stirring, and uniformly stirring to obtain a product b;

step A3, adding the product b into deionized water for dilution, uniformly stirring for later use, weighing glacial acetic acid, adding the glacial acetic acid into the deionized water for dilution, and uniformly stirring for later use;

step A4, weighing secondary amino polysiloxane, low-yellowing amino polysiloxane X, octadecyl trimethyl ammonium chloride and dodecyl dimethyl betaine, putting into an emulsification tank together, controlling the emulsification tank to stir at the speed of 50-60r/min for 15-20min, uniformly mixing all the materials, heating in a water bath to 50 ℃, adding deionized water into the emulsification tank, setting the stirring speed at 180-200r/min, and carrying out stirring reaction for 40-60min to obtain a product c;

and A5, adding the diluted product b into the product c, setting the stirring speed to be 50-60r/min, stirring and reacting for 20-30min, controlling the temperature to be 25-30 ℃, finally adding diluted glacial acetic acid, and adjusting the pH value of the mixed solution to be 5.5 to obtain the composite finishing agent.

Preferably, in the step A1, the mixing mass ratio of the dimethyl terephthalate, the ethylene glycol and the p-toluenesulfonic acid is 1: 0.8: 0.8, the mass ratio of the polyethylene glycol to the catalyst is 1:0.3, the total mass of the polyethylene glycol and the catalyst is 12 percent of the total mass of the system, and the catalyst is antimony trioxide.

Preferably, in step A2, the ratio of product a to water is 10 g: 100mL, the emulsifier is OP-15, the dosage of the emulsifier is 2g/L, the temperature of water bath heating is 60 ℃, and the mass ratio of the fat long chain to the product a is 10: 3.

Preferably, in the step A3, the mixing mass ratio of the product b and the deionized water is 1.5:1, and the mixing mass ratio of the glacial acetic acid and the deionized water is 1: 3.

Preferably, in the step A4, the mass ratio of the secondary amino polysiloxane to the low-yellowing amino polysiloxane X to the octadecyl trimethyl ammonium chloride to the dodecyl dimethyl betaine is 1:2:2:1.5, and the amount of the deionized water is twice of the total mass of the system.

A preparation method of an antistatic fabric with strong wear resistance comprises the following steps:

adding a composite finishing agent into purified water, adjusting the concentration of the composite finishing agent to be 12-13g/L, and then adjusting the pH value of the composite finishing agent to be 4-5 for later use;

pouring the treated composite finishing agent into a baking container, then carrying out pre-baking treatment on the wool fibers and the bamboo charcoal polyester fibers, then carrying out two-dipping and two-rolling treatment on the wool fibers and the bamboo charcoal polyester fibers in the composite finishing agent, setting the baking temperature at 140-155 ℃ and the baking time at 60-90s, and finishing the surface treatment on the wool fibers and the bamboo charcoal polyester fibers;

and step three, performing blending treatment on the wool fibers and the bamboo charcoal polyester fibers after surface treatment to obtain warp yarns and weft yarns, putting the warp yarns and the weft yarns into a singeing machine for singeing treatment, putting the warp yarns and the weft yarns into the slurry for soaking for 5-10min, pressing off the residual slurry, washing with clear water, naturally airing, and finally weaving the aired warp yarns and weft yarns to form the fabric, thereby obtaining the antistatic fabric with strong wear resistance.

(III) advantageous effects

The invention provides an anti-static fabric with high wear resistance and a preparation method thereof. Compared with the prior art, the method has the following beneficial effects: the composite finishing agent is used for carrying out high-temperature finishing on each fiber, under the condition of high temperature, hydrophobic groups in the product a are combined or close to the surface of the hydrophobic fiber, hydrophilic group polyether components are arranged towards one side of the air, directional arrangement is formed on the interface of the air and the fiber, the hydrophilic groups can absorb moisture in the air, and a water film with good conductivity is formed on the surface of the fiber, so that the dissipation rate of surface charges of the fabric is accelerated, the surface resistance of the fiber is reduced, and the function of eliminating static electricity is achieved;

in addition, the fat long chain is added into the composite finishing agent, so that the polyester chain segment and the polyester molecule are subjected to eutectic melting and eutectic crystallization, and the acting force is strong, so that the finished fabric still has good antistatic performance after being washed for multiple times, the antistatic effect has certain durability, and the antistatic effect of the fabric is further effectively improved.

Detailed Description

The technical solutions in the embodiments of the present invention will be clearly and completely described below, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.

Example 1:

the antistatic fabric with high wear resistance comprises the following raw materials in parts by weight: 60 parts of wool fibers, 40 parts of bamboo charcoal polyester fibers and 3 parts of a composite finishing agent;

the antistatic fabric with strong wear resistance is prepared by the following steps:

adding a composite finishing agent into purified water, adjusting the concentration of the composite finishing agent to be 12g/L, and then adjusting the pH value of the composite finishing agent to be 4 for later use;

pouring the treated composite finishing agent into a baking container, then carrying out pre-baking treatment on the wool fibers and the bamboo charcoal polyester fibers, wherein the pre-baking treatment temperature of the wool fibers and the bamboo charcoal polyester fibers is 350 ℃, then carrying out two-dipping and two-rolling treatment on the wool fibers and the bamboo charcoal polyester fibers in the composite finishing agent, setting the baking temperature to be 140 ℃ and the baking time to be 60s, and finishing the surface treatment on the wool fibers and the bamboo charcoal polyester fibers;

and step three, performing blending treatment on the wool fibers and the bamboo charcoal polyester fibers after surface treatment to obtain warp yarns and weft yarns, putting the warp yarns and the weft yarns into a singeing machine for singeing treatment, and putting the warp yarns and the weft yarns into slurry to be soaked for 5min, wherein the slurry is oxidized corn starch, ethylene glycol, sodium hydroxymethyl cellulose, chitosan and water according to a mass ratio of 2: 1: 0.2: 0.2: 6, pressing off residual size, washing with clear water, naturally drying, and finally weaving the dried warp and weft yarns to form the anti-static fabric with strong wear resistance.

The composite finishing agent is prepared by the following steps:

step A1, weighing dimethyl terephthalate, ethylene glycol and p-toluenesulfonic acid, mixing, heating the mixture until methanol in the mixture is completely distilled off, adding polyethylene glycol and a catalyst into the mixture, introducing nitrogen, and heating, wherein the mixing mass ratio of the dimethyl terephthalate, the ethylene glycol and the p-toluenesulfonic acid is 1: 0.8: 0.8, wherein the mass ratio of the polyethylene glycol to the catalyst is 1:0.3, the total mass of the polyethylene glycol and the catalyst is 12 percent of the total mass of the system, the catalyst is antimony trioxide, and the mixture is subjected to reduced pressure distillation to obtain a product a;

step A2, weighing the product a, adding the product a into a beaker, adding water into the beaker, adding an emulsifier into the beaker, uniformly stirring, heating the beaker in a water bath, adding a long fat chain into the beaker while stirring, wherein the dosage ratio of the product a to the water is 10 g: 100mL, the emulsifier is OP-15, the dosage of the emulsifier is 2g/L, the temperature of water bath heating is 60 ℃, the mass ratio of the long fat chain to the product a is 10:3, and the product b is obtained after uniform stirring;

step A3, adding the product b into deionized water for dilution, stirring uniformly for later use, weighing glacial acetic acid, adding the glacial acetic acid into the deionized water for dilution, wherein the mixing mass ratio of the product b to the deionized water is 1.5:1, and the mixing mass ratio of the glacial acetic acid to the deionized water is 1:3, and stirring uniformly for later use;

step A4, weighing secondary amino polysiloxane, low-yellowing amino polysiloxane X, octadecyl trimethyl ammonium chloride and dodecyl dimethyl betaine, putting the materials into an emulsification tank together, controlling the emulsification tank to stir at a speed of 50r/min for 15min to uniformly mix all the materials, heating in a water bath to 50 ℃, adding deionized water into the emulsification tank, wherein the mass ratio of the secondary amino polysiloxane, the low-yellowing amino polysiloxane X, the octadecyl trimethyl ammonium chloride and the dodecyl dimethyl betaine is 1:2:2:1.5, the dosage of the deionized water is twice of the total mass of the system, the stirring speed is set to be 180r/min, and stirring reaction is carried out for 40min to obtain a product c;

and A5, adding the diluted product b into the product c, setting the stirring speed to be 50r/min, stirring and reacting for 20min, controlling the temperature to be 25 ℃, finally adding diluted glacial acetic acid, and adjusting the pH value of the mixed solution to be 5.5 to obtain the composite finishing agent.

Example 2:

the antistatic fabric with high wear resistance comprises the following raw materials in parts by weight: 70 parts of wool fiber, 50 parts of bamboo charcoal polyester fiber and 5 parts of composite finishing agent;

the antistatic fabric with strong wear resistance is prepared by the following steps:

adding a composite finishing agent into purified water, adjusting the concentration of the composite finishing agent to be 13g/L, and then adjusting the pH value of the composite finishing agent to be 5 for later use;

pouring the treated composite finishing agent into a baking container, then carrying out pre-baking treatment on the wool fibers and the bamboo charcoal polyester fibers, wherein the pre-baking treatment temperature of the wool fibers and the bamboo charcoal polyester fibers is 350 ℃, then carrying out two-dipping and two-rolling treatment on the wool fibers and the bamboo charcoal polyester fibers in the composite finishing agent, setting the baking temperature to be 140 ℃ and the baking time to be 60s, and finishing the surface treatment on the wool fibers and the bamboo charcoal polyester fibers;

and step three, performing blending treatment on the wool fibers and the bamboo charcoal polyester fibers after surface treatment to obtain warp yarns and weft yarns, putting the warp yarns and the weft yarns into a singeing machine for singeing treatment, and putting the warp yarns and the weft yarns into slurry to be soaked for 5min, wherein the slurry is oxidized corn starch, ethylene glycol, sodium hydroxymethyl cellulose, chitosan and water according to a mass ratio of 2: 1: 0.2: 0.2: 6, pressing off residual size, washing with clear water, naturally drying, and finally weaving the dried warp and weft yarns to form the anti-static fabric with strong wear resistance.

The composite finishing agent is prepared by the following steps:

step A1, weighing dimethyl terephthalate, ethylene glycol and p-toluenesulfonic acid, mixing, heating the mixture until methanol in the mixture is completely distilled off, adding polyethylene glycol and a catalyst into the mixture, introducing nitrogen, and heating, wherein the mixing mass ratio of the dimethyl terephthalate, the ethylene glycol and the p-toluenesulfonic acid is 1: 0.8: 0.8, wherein the mass ratio of the polyethylene glycol to the catalyst is 1:0.3, the total mass of the polyethylene glycol and the catalyst is 12 percent of the total mass of the system, the catalyst is antimony trioxide, and the mixture is subjected to reduced pressure distillation to obtain a product a;

step A2, weighing the product a, adding the product a into a beaker, adding water into the beaker, adding an emulsifier into the beaker, uniformly stirring, heating the beaker in a water bath, adding a long fat chain into the beaker while stirring, wherein the dosage ratio of the product a to the water is 10 g: 100mL, the emulsifier is OP-15, the dosage of the emulsifier is 2g/L, the temperature of water bath heating is 60 ℃, the mass ratio of the long fat chain to the product a is 10:3, and the product b is obtained after uniform stirring;

step A3, adding the product b into deionized water for dilution, stirring uniformly for later use, weighing glacial acetic acid, adding the glacial acetic acid into the deionized water for dilution, wherein the mixing mass ratio of the product b to the deionized water is 1.5:1, and the mixing mass ratio of the glacial acetic acid to the deionized water is 1:3, and stirring uniformly for later use;

step A4, weighing secondary amino polysiloxane, low-yellowing amino polysiloxane X, octadecyl trimethyl ammonium chloride and dodecyl dimethyl betaine, putting the materials into an emulsification tank together, controlling the emulsification tank to stir at a speed of 60r/min for 20min to uniformly mix all the materials, heating in a water bath to 50 ℃, adding deionized water into the emulsification tank, wherein the mass ratio of the secondary amino polysiloxane, the low-yellowing amino polysiloxane X, the octadecyl trimethyl ammonium chloride and the dodecyl dimethyl betaine is 1:2:2:1.5, the dosage of the deionized water is twice of the total mass of the system, the stirring speed is set to be 200r/min, and stirring reaction is carried out for 60min to obtain a product c;

and A5, adding the diluted product b into the product c, setting the stirring speed to be 60r/min, stirring and reacting for 30min, controlling the temperature to be 30 ℃, finally adding diluted glacial acetic acid, and adjusting the pH value of the mixed solution to be 5.5 to obtain the composite finishing agent.

Example 3:

a preparation method of an antistatic fabric with strong wear resistance comprises the following steps:

adding a composite finishing agent into purified water, adjusting the concentration of the composite finishing agent to be 13g/L, and then adjusting the pH value of the composite finishing agent to be 4 for later use;

pouring the treated composite finishing agent into a baking container, then carrying out pre-baking treatment on the wool fibers and the bamboo charcoal polyester fibers, then carrying out two-dipping and two-rolling treatment on the wool fibers and the bamboo charcoal polyester fibers in the composite finishing agent, setting the baking temperature at 150 ℃ and the baking time at 90s, and finishing the surface treatment on the wool fibers and the bamboo charcoal polyester fibers;

and step three, performing blending treatment on the wool fibers and the bamboo charcoal polyester fibers after surface treatment to obtain warp yarns and weft yarns, putting the warp yarns and the weft yarns into a singeing machine for singeing treatment, putting the warp yarns and the weft yarns into the slurry for soaking for 10min, pressing off the residual slurry, washing with clean water, naturally airing, and finally weaving the aired warp yarns and weft yarns to form the fabric, thereby obtaining the antistatic fabric with strong wear resistance.

Comparative example:

this comparative example differs from example 1 in that no composite finish is used.

The antistatic fabrics in the examples 1-2 and the comparative example are subjected to performance tests on rubbing fastness and half-life of 30 times of washing, and the test results are as follows:

TABLE 1

	Example 1	Example 2	Comparative example
				Fastness to rubbing	4-5	4-5	2-3
Half-life period/s for 30 washes	6.88	6.53	320.51

As can be seen from table 1, the antistatic fabrics of examples 1-2 are superior to the antistatic fabrics of comparative example in rubbing fastness and 30-time half-life washing time, and therefore, the antistatic and wear-resistant properties of the fabrics can be effectively improved by the composite finishing agent.

It is noted that, herein, relational terms such as first and second, and the like may be used solely to distinguish one entity or action from another entity or action without necessarily requiring or implying any actual such relationship or order between such entities or actions. Also, the terms "comprises," "comprising," or any other variation thereof, are intended to cover a non-exclusive inclusion, such that a process, method, article, or apparatus that comprises a list of elements does not include only those elements but may include other elements not expressly listed or inherent to such process, method, article, or apparatus. Although embodiments of the present invention have been shown and described, it will be appreciated by those skilled in the art that changes, modifications, substitutions and alterations can be made in these embodiments without departing from the principles and spirit of the invention, the scope of which is defined in the appended claims and their equivalents.