Disclosure of Invention
This section is for the purpose of summarizing some aspects of embodiments of the invention and to briefly introduce some preferred embodiments. In this section, as well as in the abstract and the title of the invention of this application, simplifications or omissions may be made to avoid obscuring the purpose of the section, the abstract and the title, and such simplifications or omissions are not intended to limit the scope of the invention.
The present invention has been made in view of the above-mentioned technical drawbacks.
Therefore, as one aspect of the invention, the invention overcomes the defects in the prior art and provides a preparation method of the anion generating fabric.
In order to solve the technical problems, the invention provides the following technical scheme: a preparation method of a negative ion generation fabric comprises the following steps,
preparing a nano composite negative ion emitting material: carrying out liquid phase grinding on the negative ion emitting material in a solvent, adding low molecular weight polyethylene glycol or polyvinyl alcohol or hyperbranched polymer containing hydroxyl and carboxyl as a surface modifier, and mixing at room temperature to obtain a solution of the nano composite negative ion emitting material;
preparing a negative ion generation fabric: and compounding the solution of the nano composite negative ion emitting material with amino silicone oil to obtain the negative ion generating fabric.
As a preferred scheme of the preparation method of the negative ion generation fabric provided by the invention: the solvent comprises water, ethanol, glycol and glycerol.
As a preferred scheme of the preparation method of the negative ion generation fabric provided by the invention: the polymerization degree of the low molecular weight polyethylene glycol or polyvinyl alcohol or hyperbranched polymer containing hydroxyl and carboxyl is 600-3000.
As a preferred scheme of the preparation method of the negative ion generation fabric provided by the invention: the addition amount of the surface modifier is that the mass of the surface modifier accounts for 1-2% of the mass of the solvent.
As a preferred scheme of the preparation method of the negative ion generation fabric provided by the invention: the negative ion emission material accounts for 10% of the mass of the solvent; controlling the average grain diameter of the nano composite negative ion emitting material to be less than 100 nm.
As a preferred scheme of the preparation method of the negative ion generation fabric provided by the invention: after the surface modifier is added, the mass concentration of the negative ion emitting material in the solution of the nano composite negative ion emitting material is adjusted to be 20%, and the negative ion emitting material is compounded with amino silicone oil, wherein the amino silicone oil accounts for 0.5-5% of the mass of the nano composite negative ion emitting material.
As a preferred scheme of the preparation method of the negative ion generation fabric provided by the invention: the amino silicone oil has an ammonia value of 0.3-0.6.
As a preferred scheme of the preparation method of the negative ion generation fabric provided by the invention: the preparation method of the negative ion emitting material comprises the following steps of mixing fullerene and organic subgroup metal in a nonpolar solvent, and carrying out complex reaction, wherein the mass ratio of the fullerene to the organic subgroup metal is fullerene: organic subgroup metal 20: 1-5: 1, the obtained precipitate is the fullerene activator; crushing non-tourmaline, and controlling the average particle size of non-tourmaline powder to be less than 200 nm; mixing the prepared fullerene excitant and the non-tourmaline powder according to the following ratio of the fullerene excitant: the mass ratio of the non-tourmaline powder is 1: mixing the materials according to the proportion of 10-1000, adding a solvent, and heating for reaction to obtain the negative ion emitting material.
As a preferred scheme of the preparation method of the negative ion generation fabric provided by the invention: the organic subgroup metal comprises ethylenediamine subgroup metal compound, phosphine coordination subgroup metal compound and Fe2(EDTA)3And one or more of tetrabutyltin, wherein the non-tourmaline comprises one or more of gull rock, hexacyclic rock, palygorskite and clean water rock.
As another aspect of the invention, the invention overcomes the defects in the prior art and provides the negative ion generation fabric prepared by the preparation method.
In order to solve the technical problems, the invention provides the following technical scheme: the negative ion generation fabric prepared by the preparation method is characterized in that: the solution of the nano composite negative ion emitting material is sprayed and dried to obtain the water-based paint nano composite material, the negative ion emitting amount of the water-based paint nano composite material reaches more than 9000 per cubic centimeter, and the radiation value reaches less than 0.03 ucV.
The invention has the beneficial effects that: the preparation technology of the anion emission functional nano composite material solves the problems of low emissivity and harmful radiation of the anion emission material in the prior art, and compared with the traditional preparation method, the preparation technology has the advantages of low cost, convenient operation, controllable granularity of nano powder and high production efficiency, and can be applied to industrial production in a large scale.
Detailed Description
In order to make the aforementioned objects, features and advantages of the present invention comprehensible, embodiments accompanied with examples are described in detail below.
In the following description, numerous specific details are set forth in order to provide a thorough understanding of the present invention, but the present invention may be practiced in other ways than those specifically described and will be readily apparent to those of ordinary skill in the art without departing from the spirit of the present invention, and therefore the present invention is not limited to the specific embodiments disclosed below.
Furthermore, reference herein to "one embodiment" or "an embodiment" means that a particular feature, structure, or characteristic described in connection with the embodiment is included in at least one implementation of the invention. The appearances of the phrase "in one embodiment" in various places in the specification are not necessarily all referring to the same embodiment, nor are separate or alternative embodiments mutually exclusive of other embodiments.
Example 1:
dissolving fullerene in normal hexane to be supersaturated and dissolved, and performing centrifugal separation to prepare high-purity fullerene, wherein the size of the fullerene is 0.71 nm; the fullerene and the metal are chelated by mixing the fullerene and ethylenediamine platinum in acetone according to the ratio of 10: 1, mixing and dissolving under the pressure of 2 atmospheric pressures, heating to react for 2 hours at the temperature of 120 ℃, washing the obtained precipitate with acetone, and drying in vacuum to obtain a fullerene exciting agent; crushing for 3 times by using a jet milling method to prepare the nano-scale negative ion emitting ancient sea rock/clean water rock with the mass ratio of 1:1, compounding powder; mixing the prepared fullerene excitant with ancient sea rock/clean water stone powder according to the mass ratio of 1: 100, mixing, using water as a solvent, performing ultrasonic dispersion for 30min, reacting in a hydration kettle at 140 ℃ for 6h (under the protection of nitrogen), obtaining a negative ion emitting material, performing primary grinding in a liquid phase grinding mode, using ethanol as a liquid phase grinding medium, adding 1 wt% (the mass percentage of the polyethylene glycol in the ethanol) of polyethylene glycol with low polymerization degree and molecular weight of 600 as a surface modifier, using 10 wt% (the mass percentage of the ethanol) of the negative ion emitting material, using 90nm as an average particle size of powder, obtaining a nano composite negative ion emitting material, performing concentration, volatilizing the solvent to obtain a negative ion emitting solution with the concentration of 20 wt%, compounding the negative ion emitting solution with amino silicone oil with the ammonia value of 0.3, using the amino silicone oil with the addition ratio of 0.5 wt% of the mass of the nano composite negative ion emitting material, diluting by 10 times, performing post finishing on a terylene knitted fabric (the gram weight of 200 g) in a padding and drying mode, padding the solution to obtain the negative ion generation fabric, and measuring that the negative ion emission amount is 1900/cubic centimeter and the radiation value is 0.002 ucV.
Example 2:
dissolving fullerene in normal hexane to be supersaturated and dissolved, and performing centrifugal separation to prepare high-purity fullerene, wherein the size of the fullerene is 0.71 nm; the fullerene and the metal are chelated by mixing the fullerene and ethylenediamine platinum in acetone according to the ratio of 10: 1, mixing and dissolving under the pressure of 2 atmospheric pressures, heating to react for 2 hours at the temperature of 120 ℃, washing the obtained precipitate with acetone, and drying in vacuum to obtain a fullerene exciting agent; crushing for 3 times by using a jet milling method to prepare nano-scale negative ion emitting ancient sea rock/clean water stone compound powder with the mass ratio of 1: 1; mixing the prepared fullerene excitant with ancient sea rock/clean water stone powder according to the mass ratio of 1: 100, mixing, using water as a solvent, performing ultrasonic dispersion for 30min, reacting in a hydration kettle at 140 ℃ for 6h (under the protection of nitrogen), obtaining a negative ion emitting material, performing primary grinding in a liquid phase grinding mode, using ethanol as a liquid phase grinding medium, adding 1.5 wt% of polyethylene glycol with low polymerization degree and molecular weight of 600 as a surface modifier (the polyethylene glycol accounts for the mass percent of the ethanol), using the negative ion emitting material with the concentration of 10 wt% (accounting for the mass percent of the ethanol), using the powder with the average particle size of 90nm, obtaining the substance which is a nano composite negative ion emitting material, performing concentration, volatilizing the solvent to obtain a negative ion emitting solution with the concentration of 20 wt%, compounding the negative ion emitting solution with amino silicone oil with the ammonia value of 0.3, using the amino silicone oil with the addition ratio of 0.5% of the mass of the nano composite negative ion emitting material, diluting by 10 times, performing after-finishing on a knitted polyester fabric (with the gram, padding the solution to obtain the negative ion generation fabric, and measuring that the negative ion emission amount is 2000 per cubic centimeter and the radiation value is 0.002 ucV.
Example 3:
dissolving fullerene in normal hexane to be supersaturated and dissolved, and performing centrifugal separation to prepare high-purity fullerene, wherein the size of the fullerene is 0.71 nm; the fullerene and the metal are chelated by mixing the fullerene and ethylenediamine platinum in acetone according to the ratio of 10: 1, mixing and dissolving under the pressure of 2 atmospheric pressures, heating to react for 2 hours at the temperature of 120 ℃, washing the obtained precipitate with acetone, and drying in vacuum to obtain a fullerene exciting agent; crushing for 3 times by using a jet milling method to prepare nano-scale negative ion emitting ancient sea rock/clean water stone compound powder with the mass ratio of 1: 1; mixing the prepared fullerene excitant with ancient sea rock/clean water stone powder according to the mass ratio of 1: 100, mixing the components, performing ultrasonic dispersion for 30min, reacting in a hydration kettle at 140 ℃ for 6h (under the protection of nitrogen) to obtain a negative ion emitting material, further solving the dispersion of the nano composite negative ion emitting material and the film forming property on the surface of the fabric, performing primary grinding in a liquid phase grinding mode, wherein a liquid phase grinding medium is ethanol, 2% of polyethylene glycol with low degree of polymerization and the molecular weight of 600 is added as a surface modifier (the polyethylene glycol accounts for the mass percent of the ethanol), the concentration of the negative ion emitting material is 10 wt% (the mass percent of the ethanol), the concentration of nano powder is 10%, the average particle size of the powder is 90nm, the obtained substance is the nano composite negative ion emitting material, the solvent is volatilized after concentration to obtain a negative ion emitting solution with the concentration of 20%, the solution is compounded with amino silicone oil with the ammonia value of 0.3, the adding proportion of the amino silicone oil is 0.5% of the mass of the nano composite negative ion emitting material, diluting by 10 times, performing after-treatment on the polyester knitted fabric (the gram weight is 200 g) in a padding and drying mode, padding the solution to obtain the negative ion generation fabric, and measuring the negative ion emission quantity to be 2050/cubic centimeter and the radiation value to be 0.002 ucV.
Example 4:
dissolving fullerene in normal hexane to be supersaturated and dissolved, and performing centrifugal separation to prepare high-purity fullerene, wherein the size of the fullerene is 0.71 nm; the fullerene and the metal are chelated by mixing the fullerene and ethylenediamine platinum in acetone according to the ratio of 10: 1, mixing and dissolving under the pressure of 2 atmospheric pressures, heating to react for 2 hours at the temperature of 120 ℃, washing the obtained precipitate with acetone, and drying in vacuum to obtain a fullerene exciting agent; crushing for 3 times by using a jet milling method to prepare nano-scale negative ion emitting ancient sea rock/clean water stone compound powder with the mass ratio of 1: 1; mixing the prepared fullerene excitant with ancient sea rock/clean water stone powder according to the mass ratio of 1: 100, mixing, using water as a solvent, performing ultrasonic dispersion for 30min, reacting in a hydration kettle at 140 ℃ for 6h (under the protection of nitrogen), obtaining a negative ion emitting material, performing primary grinding in a liquid phase grinding mode, using ethanol as a liquid phase grinding medium, adding 2 wt% of polyethylene glycol with low polymerization degree and molecular weight of 600 as a surface modifier (the polyethylene glycol accounts for the mass percent of the ethanol), using the concentration of the negative ion emitting material to be 10 wt% (accounting for the mass percent of the ethanol), using the average particle size of powder to be 90nm, using the obtained substance to be a nano composite negative ion emitting material, performing concentration and volatilization on the solvent to obtain a negative ion emitting solution with the concentration of 20%, compositing the negative ion emitting solution with amino silicone oil with the ammonia value of 0.3, using the amino silicone oil with the proportion of 1% of the mass of the nano composite negative ion emitting material, diluting by 10 times, performing post-finishing on a polyester knitted fabric (with the, padding the solution to obtain the negative ion generation fabric, and measuring that the negative ion emission amount is 2050 per cubic centimeter and the radiation value is 0.002 ucV.
Example 5:
dissolving fullerene in normal hexane to be supersaturated and dissolved, and performing centrifugal separation to prepare high-purity fullerene, wherein the size of the fullerene is 0.71 nm; the fullerene and the metal are chelated by mixing the fullerene and ethylenediamine platinum in acetone according to the ratio of 10: 1, mixing and dissolving under the pressure of 2 atmospheric pressures, heating to react for 2 hours at the temperature of 120 ℃, washing the obtained precipitate with acetone, and drying in vacuum to obtain a fullerene exciting agent; crushing for 3 times by using a jet milling method to prepare nano-scale negative ion emitting ancient sea rock/clean water stone compound powder with the mass ratio of 1: 1; mixing the prepared fullerene excitant with ancient sea rock/clean water stone powder according to the mass ratio of 1: 100, mixing, ultrasonically dispersing for 30min, reacting in a hydration kettle at 140 ℃ for 6h (under the protection of nitrogen) to obtain a negative ion emitting material, grinding for the first time in a liquid phase grinding mode, wherein a liquid phase grinding medium is ethanol, 2 wt% of polyethylene glycol with low polymerization degree and molecular weight of 600 is added as a surface modifier (the polyethylene glycol accounts for the mass percent of the ethanol), the concentration of the negative ion emitting material is 10 wt% (accounts for the mass percent of the ethanol), the average particle size of powder is 90nm, the obtained substance is the nano composite negative ion emitting material, after concentration, the solvent is volatilized to obtain a negative ion emitting solution with the concentration of 20%, the negative ion emitting solution is compounded with amino silicone oil with the ammonia value of 0.3, the adding proportion of the amino silicone oil is 1.5% of the mass of the nano composite negative ion emitting material, the finishing agent after the negative ion emission is prepared is diluted by 10 times, finishing is carried out on the terylene knitted fabric (the gram weight of 200 g) in a padding and, padding the solution to obtain the negative ion generation fabric, and measuring that the negative ion emission amount is 2045/cubic centimeter and the radiation value is 0.002 ucV.
Example 6:
dissolving fullerene in normal hexane to be supersaturated and dissolved, and performing centrifugal separation to prepare high-purity fullerene, wherein the size of the fullerene is 0.71 nm; the fullerene and the metal are chelated by mixing the fullerene and ethylenediamine platinum in acetone according to the ratio of 10: 1, mixing and dissolving under the pressure of 2 atmospheric pressures, heating to react for 2 hours at the temperature of 120 ℃, washing the obtained precipitate with acetone, and drying in vacuum to obtain a fullerene exciting agent; crushing for 3 times by using a jet milling method to prepare nano-scale negative ion emitting ancient sea rock/clean water stone compound powder with the mass ratio of 1: 1; mixing the prepared fullerene excitant with ancient sea rock/clean water stone powder according to the mass ratio of 1: 100, mixing, using water as a solvent, performing ultrasonic dispersion for 30min, reacting in a hydration kettle at 140 ℃ for 6h (under the protection of nitrogen), obtaining a negative ion emission material, performing primary grinding on the negative ion emission material in a liquid phase grinding mode, using ethanol as a liquid phase grinding medium, adding 2% of polyethylene glycol with low polymerization degree and molecular weight of 600 as a surface modifier (the polyethylene glycol accounts for the mass percent of the ethanol), wherein the concentration of the negative ion emission material is 10 wt% (accounting for the mass percent of the ethanol), the average particle size of powder is 90nm, obtaining a nano composite negative ion emission material, performing concentration, volatilizing the solvent to obtain a negative ion emission solution with the concentration of 20 wt%, compounding the negative ion emission solution with amino silicone oil with the ammonia value of 0.3, diluting the amino silicone oil by 5 times in a proportion of 0.5% of the mass of the negative ion nano powder, performing after-finishing on a knitted polyester fabric (with the gram weight of 200 g) in a padding, padding the solution to obtain the negative ion generation fabric, wherein the emission quantity of the negative ions is 6850 per cubic centimeter, and the radiation value is 0.003 ucV.
Example 7:
dissolving fullerene in normal hexane to be supersaturated and dissolved, and performing centrifugal separation to prepare high-purity fullerene, wherein the size of the fullerene is 0.71 nm; the fullerene and the metal are chelated by mixing the fullerene and ethylenediamine platinum in acetone according to the ratio of 10: 1, mixing and dissolving under the pressure of 2 atmospheric pressures, heating to react for 2 hours at the temperature of 120 ℃, washing the obtained precipitate with acetone, and drying in vacuum to obtain a fullerene exciting agent; crushing for 3 times by using a jet milling method to prepare nano-scale negative ion emitting ancient sea rock/clean water stone compound powder with the mass ratio of 1: 1; mixing the prepared fullerene excitant with ancient sea rock/clean water stone powder according to the mass ratio of 1: 100, mixing, using water as a solvent, performing ultrasonic dispersion for 30min, reacting in a hydration kettle at 140 ℃ for 6h (under the protection of nitrogen), obtaining a negative ion emission material, performing primary grinding in a liquid phase grinding mode, using ethanol as a liquid phase grinding medium, adding 2% of polyethylene glycol with low polymerization degree and molecular weight of 600 as a surface modifier (the polyethylene glycol accounts for the mass percent of the ethanol), wherein the concentration of the negative ion emission material is 10 wt% (accounting for the mass percent of the ethanol), the concentration of nano powder is 10%, the average particle size of the powder is 90nm, obtaining a nano composite negative ion emission material, performing concentration, volatilizing the solvent to obtain a negative ion emission solution with the concentration of 20%, compounding the negative ion emission solution with amino silicone oil with the ammonia value of 0.3, diluting the amino silicone oil by 2 times in a proportion of 0.5% of the mass of the nano composite negative ion emission material, performing after-finishing on a polyester knitted fabric (the gram weight of 200 g) in a, padding the solution to obtain the negative ion generation fabric, and measuring that the negative ion emission amount is 16000 per cubic centimeter and the radiation value is 0.004 ucV. The hand feeling is obviously improved and softened, after an accelerated aging test at 70 ℃ is carried out for 7 days, the blank reference sample which is not subjected to surface modification and amino silicone oil treatment has no yellowing phenomenon, but the negative ion generation fabric has no yellowing phenomenon after the aging test.
Example 8:
dissolving fullerene in normal hexane to be supersaturated and dissolved, and performing centrifugal separation to prepare high-purity fullerene, wherein the size of the fullerene is 0.71 nm; the fullerene and the metal are chelated by mixing the fullerene and ethylenediamine platinum in acetone according to the ratio of 10: 1, mixing and dissolving under the pressure of 2 atmospheric pressures, heating to react for 2 hours at the temperature of 120 ℃, washing the obtained precipitate with acetone, and drying in vacuum to obtain a fullerene exciting agent; crushing for 3 times by using a jet milling method to prepare nano-scale negative ion emitting ancient sea rock/clean water stone compound powder with the mass ratio of 1: 1; mixing the prepared fullerene excitant with ancient sea rock/clean water stone powder according to the mass ratio of 1: 100, mixing, ultrasonically dispersing for 30min, reacting in a hydration kettle at 140 ℃ for 6h (under the protection of nitrogen) to obtain a negative ion emitting material, grinding for one time in a liquid phase grinding mode to further solve the dispersion of the nano composite negative ion emitting material and the film forming property on the surface of the fabric, adding 2% of polyethylene glycol with low degree of polymerization and molecular weight of 600 as a surface modifier (the polyethylene glycol accounts for the mass percent of the ethanol), wherein the concentration of the negative ion emitting material is 10 wt% (the mass percent of the ethanol), the negative ion emitting material accounts for 10% of the mass of the ethanol, the average particle size of powder is 90nm, the obtained substance is the nano composite negative ion emitting material, volatilizing the solvent after concentration to obtain a negative ion emitting solution with the concentration of 20%, and compounding the negative ion emitting solution with amino silicone oil with the ammonia value of 0.6, the adding proportion of the amino silicone oil is 0.5 percent of the mass of the nano composite negative ion emitting material, the negative ion emitting after-finishing agent is prepared and diluted by 3 times, the cotton woven fabric (the gram weight is 200 g) is subjected to after-finishing in a padding and drying mode, the solution is padded to obtain the negative ion generating fabric, the emission of the negative ions is measured to be 12600 per cubic centimeter, and the radiation value is measured to be 0.003 ucV. The hand feeling is obviously improved and softened, after an accelerated aging test at 70 ℃ is carried out for 7 days, the blank reference sample which is not subjected to surface modification and amino silicone oil treatment has no yellowing phenomenon, but the negative ion generation fabric has no yellowing phenomenon after the aging test.
The cotton fabric has higher anion generation amount due to different hydrophilic properties, and the cotton fiber has a cavity structure, so that nanoparticles can be absorbed, the dispersion of the nanoparticles is facilitated, and the adhesion of the nanoparticles can be improved, so that the anion generation amount is improved. Meanwhile, the possibility of oxidation is greatly reduced after surface modification and amino silicone oil compounding, and the problem of fabric yellowing (fabric yellowing due to amino oxidation) is effectively solved.
The preparation technology of the anion emission functional nano composite material solves the problems of low emissivity and harmful radiation of the anion emission material in the prior art, and compared with the traditional preparation method, the preparation technology has the advantages of low cost, convenient operation, controllable granularity of nano powder and high production efficiency, and can be applied to industrial production in a large scale.
It should be noted that the above-mentioned embodiments are only for illustrating the technical solutions of the present invention and not for limiting, and although the present invention has been described in detail with reference to the preferred embodiments, it should be understood by those skilled in the art that modifications or equivalent substitutions may be made on the technical solutions of the present invention without departing from the spirit and scope of the technical solutions of the present invention, which should be covered by the claims of the present invention.