COLORIMETRIC GAS SENSOR BASED ON NANOFIBER YARN FOR GAS INDICATION INCLUDING IONIC LIQUIDS AND COLOR CHANGE DYES AND METHOD OF FABRICATING SAME

Abstract

Disclosed is a colorimetric gas sensor using a complex polymer nanofiber structure for yarn-based gas indication, in which ionic liquids as effective gas adsorbents and color change dyes having varying colors have been functionalized in a nanofiber and a method of fabricating the same. In the fabrication method, after the ionic liquids and color change dyes are mixed with a polymer solution in which high-temperature stirring and quenching processes are accompanied to prepare fine crystals of color change dyes. Accordingly, the dual-electro-spinning process is conducted to produce the nanofiber yarn scaffold on which ionic liquids and color change dyes are finely functionalized.

Claims

1. A gas sensor, comprising: a polymer nanofiber in which ionic liquids accelerating an adsorption of a specific gas and color change dyes having varying colors through a reaction with molecules of the specific gas have been anchored, wherein the polymer nanofiber is wound on a support having a wire form to form a three-dimensional (3-D) network structure and form an independent yarn type structure.

2. The gas sensor of claim 1, wherein the 3-D network structure is a 3-D porous membrane structure in which the polymer nanofibers having a structure of a 1-D shape are randomly tangled on the support.

3. The gas sensor of claim 1, wherein: the ionic liquids have high solubility for the specific gas, and the ionic liquids have steam pressure of 10.sup.910.sup.12 Pa at room temperature and are left on the surface of the polymer nanofiber and are functionalized without evaporating even after electro-spinning.

4. The gas sensor of claim 1, wherein at least one of the ionic liquids are from a group consisting of 1-n-butyl-3-methylimidazolium tetrafluoroborate ([C.sub.4mim] [BF.sub.4]), 1-n-butyl-3-methylimidazolium hexafluorophosphate ([C.sub.4mim] [PF.sub.6]), 1-n-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([C.sub.4mim] [Tf.sub.2N]), 1-n-butyl-3-methylimidazolium bromide ([C.sub.4mim] [Br]), 1-ethyl-3-methylimidazolium hexafluorophosphate ([C.sub.2mim] [PF.sub.6]), 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([C.sub.2mim] [Tf.sub.2N]), 1-hexyl-3-methylimidazolium tetrafluoroborate ([C.sub.6mim] [BF.sub.4]), 1-hexyl-3-methylimidazolium hexafluorophosphate ([C.sub.6mim] [PF.sub.6]), 1-hexyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([C.sub.6mim] [Tf.sub.2N]), 1-octyl-3-methylimidazolium tetrafluoroborate ([C.sub.8mim] [BF.sub.4]), 1-octyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([C.sub.8mim] [Tf.sub.2N]), trihexyl(tetradecyl)phosphonium pyrazole ([P66614][Pyr]), trihexyl(tetradecyl)phosphonium imidazole ([P66614][Im]), trihexyl(tetradecyl)phosphonium indole ([P66614][Ind]), trihexyl(tetradecyl)phosphonium Trizole ([P66614][Triz]), trihexyl(tetradecyl)phosphonium bentrizole ([P66614][Bentriz]), trihexyl(tetradecyl)phosphonium tetrazole ([P66614][Tetz]), and trihexyl(tetradecyl)phosphonium bromide ([P66614][Br]).

5. The gas sensor of claim 1, wherein the color change dyes comprise a substance having at least one characteristic change of color, chroma, luma, and perception attributable to a frequency change of a wavelength within visible range, from visible range to infrared or ultraviolet range, from infrared or ultraviolet range to visible range, or an intensity change of a wavelength upon reaction with the molecules of the specific gas.

6. The gas sensor of claim 1, wherein at least one of the color change dyes are selected from a group consisting of lead(II) acetate(Pb(CH.sub.3COO).sub.2), iron(II) acetate(Fe(CH.sub.3COO).sub.2), nickel(II) acetate(Ni(CH.sub.3COO).sub.2), copper(II) acetate(Cu(CH.sub.3COO).sub.2), cadmium acetate(Cd(CH.sub.3COO).sub.2), cobalt(II) acetate(Co(CH.sub.3COO).sub.2), manganese(II) acetate (Cu(CH.sub.3COO).sub.2), bismuth(III) acetate(Co(CH.sub.3COO).sub.3), silver(I) acetate(Ag(CH.sub.3COO)), silver nitride (AgNO.sub.3), otolidine, m-tolidine, bromophenol blue+TBAH, methyl red+TBAH, thymol blue+TBAH, fluorescein, bromocresol purple, bromophenol red, LiNO.sub.3, 5-10-15-20-tetraphenylporphyrinatozinc (II), and 5-10-15-20-tetrakis(2,4,6-trimethylphenyl)porphyrinatozinc (II).

7. The gas sensor of claim 1, wherein the color change dyes have a diameter of 1 nm1 m.

8. The gas sensor of claim 1, wherein the polymer nanofiber is formed by electric-spinning a polymer solution comprising the ionic liquids and the color change dyes.

9. The gas sensor of claim 1, wherein: the polymer nanofiber has a diameter of 100 nm10 m, and the yarn structure has a diameter of 10 m1000 m.

10. The gas sensor of claim 1, wherein the support has diameter of 15,000 m and has tensile strength of 503,000 MPa.

11. The gas sensor of claim 1, wherein the support comprises at least one of the metals selected from a group consisting Fe, W, Ti, Cu, Ni, Zn, and stainless steel, a natural fiber selected from a group consisting cotton, linen, silk, and wool, and a man-made fiber selected from a group consisting of nylon, polyester, acryl, polyvinylalcohol polyvinylloid, polyethylene, polypropylene, polyurethane, rayon, an acetate glass fiber, and a metal fiber.

12. The gas sensor of claim 1, wherein a weight ratio of the ionic liquids is 0.1 wt %100 wt % compared to the weight of the polymer used in the polymer nanofiber.

13. The gas sensor of claim 1, wherein the weight ratio of the color change dyes has a concentration range of 0.1 wt %400 wt % compared to the weight of the polymer used in the polymer nanofiber.

14. The gas sensor of claim 1, wherein a polymer configuring the polymer nanofiber comprises at least one selected from a group consisting of polyperfuryl alcohol (PPFA), polymethyl methacrylate (PMMA), polyacryl copolymer, polyvinyl acetate (PVAc), polyvinylacetate copolymer, polystyrene (PS), polyvinylpyrrolidone (PVP), polystyrene copolymer, polyethylene oxide (PEO), polyethylene oxide copolymer, polycarbonate (PC), polyvinyl chloride (PVC), polypropyleneoxide copolymer, polycaprolactone, polyvinylfluoride, polyvinylidenefluoride (poly(vinylidene fluoride) (PVDF)), polyvinylidenefluoride copolymer, polyimide, polyacrylonitrile (PAN), 73-49 polyethylene terephthalate (PET), polypropyleneoxide (PPO), polyvinylalcohol (PVA), styrene-acrylonitrile (SAN), polycarbonate (PC), polyaniline (PANI), polypropylene (PP), and polyethylene (PE).

15. A method of fabricating a gas sensor, comprising steps of: (a) fabricating a mixed solution which the ionic liquids and color change dyes are mixed with the polymer solution which a polymer is dissolved in a solvent; (b) dissolving the ionic liquids and the color change dyes within the mixed solution through high-temperature stirring process; (c) fabricating an electro-spinning solution containing dyes recrystallized into fine crystals through quenching process of the mixed solution which the ionic liquids and the color change dyes have been dissolved; (d) fabricating a one-dimensional (1-D) polymer nanofiber in which the ionic liquids and the color change dyes have been anchored using a dual electro-spinning process and fabricating the 1-D polymer nanofiber into a nanofiber having a 3-D network structure of a yarn shape; and (e) winding and collecting the nanofiber with the 3-D network structure of a yarn shape using a winder.

16. The method of claim 15, wherein in the step (a), at least one selected from a group consisting of deionized water, tetrahydrofuran, methanol, isopropanol, formic acid, acetonitrile, nitromethane, acetic acid, ethanol, acetone, ethylene glycol (EG), dimethyl sulfoxide (DMSO), dimethylformamide (DMF), 73-51 dimethylacetamide (DMAc) and toluene is used as the solvent.

17. The method of claim 15, wherein in the step (a), the polymer is fabricated to have a weight ratio of 0.1 wt %90 wt % in the solvent.

18. The method of claim 15, further comprising a step of inducing liquefaction of lead (II) acetate trihydrate by stirring the mixed solution at a temperature of 75 C. or higher if lead(II) acetate is used as the color change dyes is used in the step (b).

19. The method of claim 15, wherein the step (c) comprises re-crystallizing of the color change dyes by quenching the mixed solution in which the color change dyes have been liquefied in advance at a temperature of 85 C. or higher through high-temperature stirring process.

20. The method of claim 15, wherein in the step (d), in the dual electro-spinning process, an amount of discharge of a spinning solution is 0.1100 l/min and a voltage of 130 kV is applied between a needle of a syringe and a current collector, and the current collector is rotated at 10500 rpm, the 1-D polymer nanofiber that is dually spun is wound on a support of a wire form positioned at a core of the rotation to form the nanofiber having a 3-D network structure of an independent yarn type structure.

21. The method of claim 15, wherein in the step (e), the wound nanofiber having the 3-D network structure of an independent yarn type structure is wound and collected at a velocity range of 1400 mm/min using a winder.

22. The method of claim 15, wherein the gas sensor detects at least one of H.sub.2S, SO.sub.x, NO.sub.x and CO.sub.x and at least one of CH.sub.3COCH.sub.3, C.sub.2H.sub.5OH and C.sub.6H.sub.5CH.sub.3.

23. The method of claim 15, wherein the gas sensor has a color change on a surface of the gas sensor due to adsorption and a surface chemical reaction between the specific gas and the color change dyes when the gas sensor is exposed to the specific gas.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0027] The accompany drawings, which are included as a part of the detailed description in order to help understanding of embodiments, provide embodiments of the present invention and describe the technical characteristics of the present invention along with the detailed description.

[0028] FIG. 1 is a diagram of a colorimetric gas sensor based on a complex polymer nanofiber yarn for gas indication in which ionic liquids and color change dyes have been anchored in a 1-D nanofiber structure according to an embodiment.

[0029] FIG. 2 illustrates a process of fabricating the colorimetric gas sensor based on a complex polymer nanofiber yarn for gas indication in which the ionic liquids and the color change dyes have been anchored in the 1-D nanofiber structure using a dual electro-spinning process according to an embodiment.

[0030] FIG. 3 is a flowchart illustrating a method of fabricating the colorimetric gas sensor based on a complex polymer nanofiber yarn for gas indication, in which the ionic liquids and the color change dyes have been anchored in the 1-D nanofiber structure using a dual electro-spinning process, and a high-temperature stirring and quenching process according to an embodiment 1.

[0031] FIG. 4 illustrates photos of a colorimetric gas sensor based on a complex polymer nanofiber yarn for gas indication, in which ionic liquids (trihexyl(tetradecyl)phosphonium bromide) having (a-c) 20 wt %, (d-f) 40 wt %, (g-i) 80 wt % content and color change dyes (lead(II) acetate) having the same content (e.g., 160 wt %) compared to a polymer weight were anchored, which were photographed by a scanning electron microscope according to an embodiment.

[0032] FIG. 5 illustrates photos of a colorimetric gas sensor based on a complex polymer nanofiber yarn for gas indication in which ionic liquids are not included and color change dyes (lead(II) acetate) of 160 wt % compared to a polymer weight were anchored, fabricated according to a comparative example 1, which were photographed by a scanning electron microscope.

[0033] FIG. 6 illustrates photo images of color change degrees obtained by exposing, to hydrogen sulfide gas, a colorimetric gas sensor based on a complex polymer nanofiber yarn for gas indication, in which ionic liquids (trihexyl(tetradecyl)phosphonium bromide) of 20, 40, and 80 wt % and color change dyes (lead(II) acetate) of 160 wt % compared to a polymer weight were anchored, fabricated according to an embodiment 1, and a colorimetric gas sensor based on a complex polymer nanofiber yarn for gas indication, in which only color change dyes (lead(II) acetate) of 160 wt % compared to a polymer weight was anchored, fabricated according to a comparative example 1, at 5 ppm for 0, 10, 20, 30, 40, 50, and 60 seconds.

[0034] FIG. 7 is a graph quantitatively illustrating color change degrees (RGB changes) before and after the exposure of hydrogen sulfide gas for each exposure time of each sample in order to quantitatively analyze more precise color changes based on the photo images of FIG. 6.

[0035] FIG. 8 illustrates photo images of color change degrees obtained if hydrogen sulfide gases of 5, 4, 3, 2, and 1 ppm are exposed for 60 seconds, and if an exposure time at 1 ppm was adjusted to 60, 50, 40, 30, 20, and 10 seconds with respect to a colorimetric gas sensor based on a complex polymer nanofiber yarn for gas indication, in which ionic liquids (trihexyl(tetradecyl)phosphonium bromide) of 40 wt % and color change dyes (lead(II) acetate) of 160 wt % compared to a polymer weight were anchored, determined to have the most excellent color change characteristics based on the results of FIGS. 6 and 7 among samples fabricated according to an embodiment 1, and a colorimetric gas sensor based on a complex polymer nanofiber yarn for gas indication, in which only color change dyes (lead(II) acetate) of 160 wt % compared to a polymer weight was anchored, fabricated according to a comparative example 1.

[0036] FIG. 9 is a graph quantitatively illustrating color change degrees (RGB changes) before and after the exposure to hydrogen sulfide gas for each concentration and each exposure time of each sample in order to quantitatively analyze more precise color changes based on the photo images of FIG. 8.

[0037] FIG. 10 illustrates photo images of color change degrees obtained before and after a colorimetric gas sensor based on a complex polymer nanofiber yarn for gas indication, in which ionic liquids (trihexyl(tetradecyl)phosphonium bromide) of 40 wt % and color change dyes (lead(II) acetate) of 160 wt % compared to a polymer weight were anchored, determined to have the most excellent color change performance among samples fabricated according to an embodiment 1, was exposed to exhaled breaths of 8 healthy persons, collected in respective Tedlar bags, and to a simulated halitosis patient exhaled breath mixed with hydrogen sulfide gas of a 1 ppm concentration for 1 minute.

[0038] FIG. 11 is a graph quantitatively illustrating color change degrees (RGB sums) before and after the exposure to simulated halitosis breath patients' exhaled breath for each person in order to quantitatively analyze more precise color changes based on the photo images of FIG. 10.

DETAILED DESCRIPTION

[0039] The present invention may be modified in various ways, and may have various embodiments. Hereinafter, specific embodiments are described in detail based on the accompanying drawings.

[0040] In describing the present invention, a detailed description of a related known technology will be omitted if it is deemed to make the gist of the present invention unnecessarily vague.

[0041] Terms, such as the first and the second, may be used to describe various elements, but the elements are not restricted by the terms. The terms are used to only distinguish one element from the other element.

[0042] Hereinafter, a colorimetric gas sensor based on a complex polymer nanofiber yarn for gas indication, including ionic liquids and color change dyes, and a method of fabricating the same, are described in detail with reference to the accompanying drawings.

[0043] In general, a colorimetric gas sensor can easily monitor and detect whether specific gas molecules are present and the concentration of specific gas molecules through the quantitative analysis of a color change degree because the specific gas molecules are absorbed by color change dyes and the color of the dyes are changed due to a chemical reaction. Furthermore, the colorimetric gas sensor has advantages in that it does not require a special electric device, can be easily reduced in size, has excellent portability, and requires a short detection time. However, since a concentration of the limit of detection of the colorimetric gas sensor is much higher than that of other gas sensors, research of a colorimetric gas sensor for improving a high concentration of the limit of detection is actively carried out.

[0044] The existing colorimetric gas sensor chiefly uses a method of simply anchoring color change dyes in a polymer by using dip-coating method in order to prevent the color change dyes from being detached out of a product during use. In the existing composition method, however, it is difficult to achieve excellent color change performance because color change dyes are rarely anchored uniformly on a color change membrane and the color change membrane does not have a sufficient specific surface area and porosity. Furthermore, an excessive amount of color change dyes needs to be used to achieve color change performance having a specific level. A colorimetric gas sensor is chiefly used as a disposable product because a color change in color change dyes is commonly irreversible. Furthermore, the colorimetric gas sensor has a danger of causing environmental pollution because heavy metal elements are included in many color change dyes.

[0045] Accordingly, in order for the colorimetric gas sensor to be widely commercialized, an ideal environment in which color change dyes cause a sharp color change through an effective and fast surface chemical reaction with a target gas even though very small amount of the color change dyes is used. Furthermore, there is a need for a colorimetric gas sensor having high sensitivity and fast response speed under the conditions. A colorimetric gas sensor for healthcare requires high sensitivity and selectivity. The colorimetric gas sensor needs to have an open structure in which the diffusion of gas is easy so that color change dyes can easily react with target gas molecules because specific gas molecules cause a color change through an adsorption and surface chemical reaction with the surface of the color change dyes. Accordingly, if a nanostructure having a high specific surface area and porosity is used as a membrane for a colorimetric gas sensor, colorimetric gas sensor sensitivity significantly improved compared to a material having a simple film form may be expected.

[0046] An example of the colorimetric gas sensor includes a hydrogen sulfide (H.sub.2S) colorimetric gas sensor for gas indication. Hydrogen sulfide is a biomarker gas for a halitosis breath. The exhaled breath of a normal person includes hydrogen sulfide (5080 ppb). In contrast, in the case of a halitosis patient, a hydrogen sulfide gas having a high concentration of a 12 ppm level is included in the exhaled breath. In this case, lead(II) acetate may become the color change dye capable of selectively detecting the hydrogen sulfide gas. However, a hydrogen sulfide colorimetric gas sensor for gas indication may be used for industrial sites because it has a high limit of detection of 5 ppm level, which is not sensitive enough to be applied to a colorimetric gas sensor for healthcare applications.

[0047] In order to improve the sensitivity of a colorimetric gas sensor, it is necessary to maximize a surface area where color change dyes are exposed to the air and to have many reaction sites. A colorimetric gas sensor having a film form has low efficiency and sensitivity for use of color change dyes because a chemical reaction is chiefly concentrated on a surface of a film and color change dyes within the film do not participate in the reaction.

[0048] Accordingly, an embodiment provides a color change sensor based on a complex polymer nanofiber yarn for gas indication, in which ionic liquids capable of accelerating the adsorption of specific gas molecules and color change dyes having a varying color through a reaction with the specific gas molecules have been anchored, and a method of fabricating the same. The surface area where the color change dyes are exposed to a target gas can be significantly increased because the color change dyes are anchored in a nanofiber yarn-based membrane having a 3-D open pore structure. Furthermore, the diffusion of target gas can be facilitated, and the color change sensor may have much deeper color change intensity than a 2-D film type color change sensor. Furthermore, there is provided an independent type colorimetric gas sensor based on a high-performance nanofiber yarn, which can accelerate reaction characteristics with color change dyes because the adsorption property of specific gas molecules are increased by introducing ionic liquids, and a method of fabricating the colorimetric gas sensor.

[0049] According to embodiments, a nanostructure having various pores that is not a substance having such a film form can be fabricated, and a gas sensor, in which such nanostructures form a 3-D network structure and have independent type fiber forms in a thread form, can be fabricated. Such a gas sensor may be applied to environments having various curves, and may also be applied as a wearable type colorimetric gas sensor in combination with textiles.

[0050] An embodiment provides a complex polymer nanofiber (yarn-based) colorimetric gas sensor for gas indication, wherein 1-D nanofibers, each one including color change dyes causing a color change capable of being visually identified through a reaction with specific gas molecules and ionic liquids capable of selectively adsorbing a specific gas because they have high solubility for the specific gas, are tangled together to form an independent type nanofiber yarn network structure having a thread form, and a method of fabricating the colorimetric gas sensor.

[0051] There may be provided a complex polymer nanofiber, within which ionic liquids and color change dyes have been uniformly anchored and, in which the ionic liquids and the color change dyes have been uniformly anchored on a surface thereof using an electro-spinning process. The complex polymer nanofibers are wound on a support of a wire form positioned in a core through multi-electro-spinning and the rotation of a current collector, thereby being capable of fabricating a sensor having an independent type yarn structure.

[0052] In an embodiment, a nanofiber yarn is basically configured with a porous nanofiber network having a high specific surface area and excellent gas diffusion. The area, in which color change dyes are exposed to the air, can be maximized by uniformly anchoring the color change dyes in a nanofiber.

[0053] In general, content of color change dyes needs to be minimized and colorimetric gas sensor characteristics need to be maximized because most color change dyes are harmful to the environment. That is, it is necessary to create an optimal environment for increasing reactivity between specific gas molecules and color change dyes. For example, there may be introduced a substance capable of improving the surface adsorption property of specific gas molecules. If a specific gas can be selectively adsorbed, the surface chemical reaction between color change dyes and the adsorbed gas can be accelerated. Accordingly, a maximized color change characteristic can be expected even with minimum color change dyes content.

[0054] An embodiment provides a method of fabricating a colorimetric gas sensor having an independent type yarn structure of a thread form, wherein ionic liquids and color change dyes are uniformly anchored on a 1-D nanofiber using a multi-electro-spinning method and the nanofibers are wound in a bundle form. A gas sensor using such a fabrication method can provide an environment in which the reactivity of color change dyes can be improved by exposing the color change dyes to a surface of a complex nanofiber as much as possible and increasing adsorption property for specific gas molecules through ionic liquids. Accordingly, a color change characteristic having high sensitivity can be induced even with minimum content of color change dyes.

[0055] Embodiments are described more specifically compared to comparative examples. The embodiments and the comparative examples are merely for describing the present invention, and the present invention is not limited to the following examples.

[0056] FIG. 1 is a diagram illustrating a colorimetric gas sensor 101 based on a complex polymer nanofiber yarn according to an embodiment of the present invention.

[0057] The colorimetric gas sensor 101 based on a complex polymer nanofiber yarn has polymer nanofibers 102 wound in a 3-D network structure in a bundle form. The polymer nanofiber 102 may include color change dyes 103 having a varying change through adsorption and reactions with specific gas molecules and ionic liquids 104 which induce the adsorption of a specific gas. In this case, in the colorimetric gas sensor 101 based on a complex polymer nanofiber yarn, 1-D nanofibers tangled together randomly may be wound in a bundle form to form a nanofiber yarn structure having a thread form.

[0058] A frequency change of a wavelength performed within a visible ray area (380-780 nm) after adsorption and reactions with a specific gas, a frequency change of a wavelength from a visible ray area to an infrared area (>780 nm) or an ultraviolet area (<380 nm), a frequency change of a wavelength from an infrared area or ultraviolet area to a visible ray area or a change in the color change characteristic, such as color, chroma, luma or perception, due to a change in the amplitude of a wavelength may occur in the polymer nanofiber 102. The color change dyes 103 whose range of an average diameter is 1 nm1 m can be uniformly anchored without aggregation in the polymer nanofiber 102. For example, one or two kinds of mixtures selected from the group consisting of lead(II) acetate(Pb(CH.sub.3COO).sub.2), iron(II) acetate(Fe(CH.sub.3COO).sub.2), nickel(II) acetate(Ni(CH.sub.3COO).sub.2), copper(II) acetate(Cu(CH.sub.3COO).sub.2), cadmium acetate(Cd(CH.sub.3COO).sub.2), cobalt(II) acetate(Co(CH.sub.3COO).sub.2), manganese(II) acetate(Cu(CH.sub.3COO).sub.2), bismuth(III) acetate(Co(CH.sub.3COO).sub.3), silver(I) acetate(Ag(CH.sub.3COO)), silver nitride (AgNO.sub.3), otolidine, m-tolidine, bromophenol blue+TBAH, methyl red+TBAH, thymol blue+TBAH, fluorescein, bromocresol purple, bromophenol red, LiNO.sub.3, 5-10-15-20-tetraphenylporphyrinatozinc (II), 5-10-15-20-tetrakis(2,4,6-trimethylphenyl)porphyrinatozinc (II) may be used as the color change dyes 103.

[0059] Furthermore, the ionic liquids 104 capable of improving the adsorption property of a specific gas by increasing the solubility of the specific gas are uniformly distributed in the polymer nanofiber 102. In this case, at least one kind selected from the group consisting of 1-n-butyl-3-methylimidazolium tetrafluoroborate ([C.sub.4mim] [BF.sub.4]), 1-n-butyl-3-methylimidazolium hexafluorophosphate ([C.sub.4mim] [PF.sub.6]), 1-n-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([C.sub.4mim] [Tf.sub.2N]), 1-n-butyl-3-methylimidazolium bromide ([C.sub.4mim] [Br]), 1-ethyl-3-methylimidazolium hexafluorophosphate ([C.sub.2mim] [PF.sub.6]), 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([C.sub.2mim] [Tf.sub.2N]), 1-hexyl-3-methylimidazolium tetrafluoroborate ([C.sub.6mim] [BF.sub.4]), 1-hexyl-3-methylimidazolium hexafluorophosphate ([C.sub.6mim] [PF.sub.6]), 1-hexyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([C.sub.6mim] [Tf.sub.2N]), 1-octyl-3-methylimidazolium tetrafluoroborate ([C.sub.8mim] [BF.sub.4]), 1-octyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([C.sub.8mim] [Tf.sub.2N]), trihexyl(tetradecyl)phosphonium pyrazole ([P66614][Pyr]), trihexyl(tetradecyl)phosphonium imidazole ([P66614][Im]), trihexyl(tetradecyl)phosphonium indole ([P66614][Ind]), trihexyl(tetradecyl)phosphonium Trizole ([P66614][Triz]), trihexyl(tetradecyl)phosphonium bentrizole ([P66614][Bentriz]), trihexyl(tetradecyl)phosphonium tetrazole ([P66614][Tetz]), trihexyl(tetradecyl)phosphonium bromide ([P66614][Br]), for example, may be used as the ionic liquids 104.

[0060] The diameter of the polymer nanofiber 102 produced through an electro-spinning process may be included in a range of 100 nm10 m. The color change dyes 103 of the listed acetate series are dyes capable of showing a specific color change through a reaction with a hydrogen sulfide gas, in particular. In addition to the listed dyes, color change dyes that cause a color change characteristic through a selective reaction and combination with a specific gas may be unlimitedly used in a combination with the nanofiber 102 including the ionic liquids 104.

[0061] FIG. 2 is a diagram of a device for a nanofiber yarn composition through multi-electro-spinning used in an embodiment 1 of the present invention.

[0062] An electro-spinning solution including the ionic liquids and color change dyes may be discharged from the needles of two different syringes 201 and 202 through an electro-spinning process, and may be discharged in the form of a 1-D complex polymer nanofiber membrane. A strong electric field from a high voltage application device is applied to the needles of the syringes 201 and 202. The discharged electro-spinning solution is spun on a current collector 203. In this case, complex polymer nanofibers spun from the two syringes 201 and 202 may be wound on a surface of a thread 204 at a core by the rotation of the current collector 203 in a yarn form. The wound complex polymer nanofiber yarn may be wound by a winder 205 and collected in a thread form.

[0063] One or two kinds of mixed solvents selected from the group consisting of deionized water, tetrahydrofuran, methanol, isopropanol, formic acid, acetonitrile, nitromethane, acetic acid, ethanol, acetone, ethylene glycol (EG), dimethyl sulfoxide (DMSO), dimethylformamide (DMF), dimethylacetamide (DMAc) and toluene(toluene), for example, may be used as a solvent used when the polymer spinning solution is fabricated.

[0064] Furthermore, one or two kinds of mixtures selected from the group consisting of polyperfuryl alcohol (PPFA), polymethyl methacrylate (PMMA), polyacryl copolymer, polyvinyl acetate (PVAc), polyvinylacetate copolymer, polystyrene (PS), polyvinylpyrrolidone (PVP), polystyrene copolymer, polyethylene oxide (PEO), polyethylene oxide copolymer, polycarbonate (PC), polyvinyl chloride (PVC), polypropyleneoxide copolymer, polycaprolactone, polyvinylfluoride, polyvinylidenefluoride (poly(vinylidene fluoride) (PVDF)), polyvinylidenefluoride copolymer, polyimide, polyacrylonitrile (PAN), 73-49 polyethylene terephthalate (PET), polypropyleneoxide (PPO), polyvinylalcohol (PVA), styrene-acrylonitrile (SAN), polycarbonate (PC), polyaniline (PANI), polypropylene (PP) and polyethylene (PE), for example, may be used as the polymer.

[0065] In order to achieve the viscosity suitable for performing electro-spinning, the polymer configuring the electro-spinning solution may be fabricated in a concentration range of a weight ratio 0.190 wt % in a specific solvent. The weight ratios of the ionic liquids and the color change dyes may have concentration ranges of 0.1100 wt % and 0.1400 wt %, respectively, compared to a polymer matrix.

[0066] The ionic liquids and color change dyes may be distributed and used in a polymer solution, in which the polymer is dissolved in the solvent, or a polymer solution refined and re-crystallized from color change dyes because a mixed electro-spinning solution experiences a high-temperature stirring and quenching process may be used for the ionic liquids and color change dyes.

[0067] Furthermore, the high-temperature stirring and quenching process may include a process of dissolving color change dyes in a solvent by stirring a mixed electro-spinning solution in which the color change dyes, ionic liquids and a polymer have been dissolved in the solvent at a melting point or higher of the color change dyes, and quenching the mixed electro-spinning solution at temperature of 25 C. or lower after the stirring for a sufficient time.

[0068] In the electro-spinning process, the amount of discharge for discharging the electro-spinning solution may have a range of 0.1100 l/min. This may be properly selected depending on the viscosity of a spinning solution. The diameter of the nanofiber that is finally composed may be controlled by adjusting a ratio of a concentration of the spinning solution and an injection speed. A voltage of a 130 kV range may be applied between the nozzle and the current collector. The distance between the nozzle and the current collector may be selected in a range of 130 cm. The rotation velocity of the current collector at which the nanofiber yarn is composed may be selected in a range of 10500 rpm, and the composed nanofiber yarn may be collected at the velocity of 1400 mm/min through the winder.

[0069] If the colorimetric gas sensor based on a complex polymer nanofiber yarn, in which the ionic liquids and the color change dyes have been anchored, is exposed to a specific gas, the adsorption of the molecules of the specific gas on a surface of each fiber is accelerated due to an ionic liquid effect. A color change may appear due to a surface chemical reaction between the adsorbed gas molecules and the color change dyes. The colorimetric gas sensor based on a complex polymer nanofiber yarn for gas indication detects environment noxious gases (e.g., H.sub.2S, SO.sub.x, NO.sub.x, CO.sub.x) and a biomarker gas (e.g., CH.sub.3COCH.sub.3, C.sub.2H.sub.5OH, C.sub.6H.sub.5CH.sub.3) included in the exhaled breath of a person.

[0070] FIG. 3 is a flowchart illustrating a method of fabricating a colorimetric gas sensor based on a complex polymer nanofiber yarn, in which ionic liquids and color change dyes have been anchored through a multi-electro-spinning process according to an embodiment of the present invention.

[0071] The fabrication method may include the step 301 of fabricating an electro-spinning solution, in which ionic liquids and color change dyes are mixed in a polymer solution having a polymer dissolved in a solvent, the step 302 of dissolving the color change dyes through high-temperature stirring at a melting point or more of the color change dyes and fabricating a complex electro-spinning solution containing color change dyes re-crystallized into fine crystals through a subsequent quenching process, the step 303 of composing a color change sensor based on a complex polymer nanofiber yarn, in which the ionic liquids and color change dyes have been anchored using a multi-electro-spinning process, and the step 304 of winding and collecting the color change sensor based on a composed complex polymer nanofiber yarn in a thread form.

[0072] The present invention is described below specifically in connection with embodiments and comparative examples. The embodiments and the comparative examples are merely from describing the present invention, and the present invention is not limited to them.

Embodiment 1: Fabrication of a Colorimetric Gas Sensor Based on a Complex Polymer Nanofiber Yarn for Gas Indication, Including Ionic Liquids and Color Change Dyes, Using a Dual Electro-Spinning Process Including Ionic Liquids and Color Change Dyes

[0073] First, in order to prepare an electro-spinning solution to be injected into a syringe, polyacrylonitrile (PAN) 0.75 g having molecular weight of 130,000 g/mol is dissolved in dimethylformamide (DMF) of 9 ml. Additionally, ionic liquids (trihexyl(tetradecyl)phosphonium bromide) of 20, 40, and 80 wt % compared to a polymer weight ratio and lead(II) acetate of 160 wt % compared to the polymer weight ratio are included in a polymer/solvent complex solution, and a spinning solution is fabricated by stirring the polymer/solvent complex solution at 500 rpm for 12 hours at a high temperature of 85 C. The color change dyes (lead(II) acetate) are dissolved through sufficient stirring at high temperature. The refinement and re-crystallization of the dissociated color change dyes (lead(II) acetate) are induced by quenching an electro-spinning solution in which the polymer (PAN) and the ionic liquids (trihexyl(tetradecyl)phosphonium bromide) have been dissolved in the solvent (DMF) at a temperature of about 25 C. The spinning solution fabricated through the high temperature stirring and quenching process is contained in each of two different syringes (e.g., Henke-Sass Wolf, 12 ml NORM-JECT). The syringes are connected to syringe pumps. The electro-spinning solutions are pushed at a discharge velocity of 10 l/min. Electro-spinning is performed by applying a voltage of 12 kV between a nozzle (23 gauge) used in a spinning process and a current collector for collecting a nanofiber. In this case, the discharged nanofiber is collected on the current collector of a hopper form that rotates at about 300 rpm. The nanofiber is wound on a support of a wire form at a velocity of 100 mm/min, and is wound and collected on a winder in a yarn structure having a thread form.

[0074] FIG. 4 illustrates photos of a scanning electron microscope with respect to a complex polymer nanofiber yarn for gas indication, which was fabricated according to an embodiment 1 of the present invention and in which ionic liquids (trihexyl(tetradecyl)phosphonium bromide) of (a-c) 20 wt %, (d-f) 40 wt %, and (g-i) 80 wt % compared to a polymer weight were included and color change dyes (lead(II) acetate) having the same content (e.g., 160 wt %) were anchored.

[0075] From the photos of the scanning electron microscope for the complex polymer nanofiber yarn fabricated through electro-spinning, that includes the ionic liquids and the color change dyes, it can be seen that the color change dyes (lead(II) acetate) having a size range of 1 m or less are well anchored in a polymer nanofiber having a diameter of about 400600 nm. In particular, the diameter of the nanofiber tends to increase on average as the content of the ionic liquids (trihexyl(tetradecyl)phosphonium bromide) increases. The reason for this is that the diameter of the nanofiber is proportional to the viscosity of the electro-spinning solution and the viscosity of the ionic liquids (trihexyl(tetradecyl)phosphonium bromide) is very high. All nanofiber yarns fabricated regardless of the content of the ionic liquids (trihexyl(tetradecyl)phosphonium bromide) have the same size of about 600 m (see (a), (d) and (g) of FIG. 4).

Comparative Example 1. Fabrication of a Colorimetric Gas Sensor Based on a Complex Polymer Nanofiber Yarn for Gas Indication, that Includes Color Change Dyes Using a Dual Electro-Spinning Process; Including Only the Color Change Dyes Other than Ionic Liquids

[0076] In the comparative example 1 compared to the embodiment 1, a color change sensor based on a complex polymer nanofiber yarn for gas indication, in which only color change dyes (lead(II) acetate) have been anchored on a polymer nanofiber by electrically spinning an electro-spinning solution, including the color change dyes having the same amount as those of the embodiment 1, but without including ionic liquids, may be fabricated. Specifically, first, polyacrylonitrile (PAN) 0.75 g having a molecular weight of 130,000 g/mol is dissolved in dimethylformamide (DMF) of 9 ml. Additionally, lead(II) acetate of 160 wt % compared to a polymer weight ratio is included in a polymer/solvent complex solution, and a spinning solution is fabricated by stirring the polymer/solvent complex solution at 500 rpm for 12 hours at a high temperature of 85 C. The color change dyes (lead(II) acetate) are dissociated through sufficient stirring. The refinement and re-crystallization of the dissociated color change dyes (lead(II) acetate) are induced by quenching an electro-spinning solution in which the polymer (PAN) has been dissolved in the solvent (DMF) at a temperature of about 25 C. The spinning solution fabricated through the high-temperature stirring and quenching process is contained in each of two different syringes (e.g., Henke-Sass Wolf, 12 ml NORM-JECT). The syringe is connected to a syringe pump. The electro-spinning solution is pushed at a discharge velocity of 10 l/min. Electro-spinning is performed by applying a voltage of 12 kV between a nozzle (or needle, 23 gauge) used for the spinning process and a current collector for collecting a nanofiber. In this case, the discharged nanofiber is collected on the current collector of a hopper form that rotates at about 300 rpm. The collected nanofiber is wound on a support of a wire form at a velocity of 100 mm/min and wound and collected on a winder in a yarn structure having a thread form.

[0077] FIG. 5 illustrates photos of a scanning electron microscope for a complex polymer nanofiber yarn for gas indication, which was fabricated according to the comparative example 1 of the present invention and in which color change dyes (lead(II) acetate) of 160 wt % compared to a polymer weight were included.

[0078] It may be seen that the diameter of a nanofiber yarn is about 600 m level and is similar to the case where the ionic liquids are included (see (a) of FIG. 5), but the diameter of a composed nanofiber is a 200 nm level and is much thinner than that of the case where the ionic liquids are included (about 500 nm) because the ionic liquids having very high viscosity are not included and thus the viscosity of an electro-spinning solution is relatively lower than the sample fabricated according to an embodiment 1. Furthermore, it can be seen that the color change dyes have been unevenly anchored on the surface of the nanofiber as in the embodiment 1 (see (b) and (c) of FIG. 5).

Experimental Example 1. Evaluation of Hydrogen Sulfide Gas Detection Color Change Characteristics Using the Colorimetric Gas Sensor Based on a Complex Polymer Nanofiber Yarn for Gas Indication, Including Ionic Liquids and Color Change Dyes Composed According to the Embodiment 1, and the Colorimetric Gas Sensor Based on a Complex Polymer Nanofiber Yarn for Gas Indication, Including Only the Color Change Dyes Composed According to the Comparative Example 1

[0079] Color change characteristics for a hydrogen sulfide gas are evaluated by directly exposing the color change sensors based on a nanofiber yarn obtained according to the embodiment 1 and comparative example 1, to the hydrogen sulfide gas, while controlling the concentration and exposure time of the hydrogen sulfide gas in a high-humidity environment having relative humidity of 80% which is a similar condition as the exhaled breath of human.

[0080] FIG. 6 illustrates photo images of color change degrees obtained by directly exposing, to a hydrogen sulfide gas of 5 ppm, the colorimetric gas sensor based on a nanofiber yarn, in which ionic liquids (trihexyl(tetradecyl)phosphonium bromide) of 20, 40, and 80 wt % compared to a polymer weight are included and color change dyes (lead(II) acetate) of 160 wt % compared to the polymer weight were anchored, fabricated according to the embodiment 1, and the colorimetric gas sensor based on a nanofiber yarn, in which only color change dyes (lead(II) acetate) of 160 wt % compared to a polymer weight was anchored, fabricated according to the comparative example 1, under conditions of 0, 10, 20, 30, 40, 50, and 60 seconds.

[0081] FIG. 6 illustrates photo images of color change degrees obtained by direct exposure to hydrogen sulfide gas of 5 ppm, of the colorimetric gas sensor based on a nanofiber yarn in which ionic liquids (trihexyl(tetradecyl)phosphonium bromide) of 20, 40, and 80 wt % compared to the polymer weight are included and color change dyes (lead(II) acetate) of 160 wt % compared to the polymer weight were anchored, fabricated according to the embodiment 1, and the colorimetric gas sensor based on a nanofiber yarn in which only color change dyes (lead(II) acetate) of 160 wt % compared to a polymer weight was anchored, fabricated according to the comparative example 1, under exposure conditions of 0, 10, 20, 30, 40, 50, and 60 seconds.

[0082] From the photo images of FIG. 6, it can be seen that the color change degree gradually grows greater as the exposure time is increased for the hydrogen sulfide concentration of 5 ppm. Furthermore, it may be seen that in the case of the sensor including the ionic liquids (trihexyl(tetradecyl)phosphonium bromide), a color change degree is much greater compared to the sensor not including the ionic liquids (trihexyl(tetradecyl)phosphonium bromide). The reason for this is that the ionic liquids (trihexyl(tetradecyl)phosphonium bromide) may accelerate the color change through a surface chemical reaction with the color change dyes (lead(II) acetate) anchored on the surface of the nanofiber yarn by improving the adsorption property of hydrogen sulfide gas as the ionic liquids have high solubility for the hydrogen sulfide gas. However, if the content of the ionic liquids (trihexyl(tetradecyl)phosphonium bromide) increases too much, color change degree is decreased because a color change becomes light-brown not thick-brown due to the unique color of the ionic liquids (trihexyl(tetradecyl)phosphonium bromide). Furthermore, if the content of the ionic liquids (trihexyl(tetradecyl)phosphonium bromide) increases too much, electro-spinning is not smoothly performed because the viscosity of the electro-spinning solution increases too much. It is seen that the ideal content of the ionic liquids (trihexyl(tetradecyl)phosphonium bromide) is present.

[0083] FIG. 7 is a graph quantitatively illustrating color change degrees (RGB changes) before and after the exposure to 5 ppm hydrogen sulfide for 0, 10, 20, 30, 40, 50, and 60 seconds as in the photo images of FIG. 6, for the purpose of clearer color change quantitative analysis of the color change images illustrated in FIG. 6. It may be seen that for the sensors including the ionic liquids (trihexyl(tetradecyl)phosphonium bromide) of 20, 40, and 80 wt %, respectively, compared to the polymer weight, the sum of RGB changes is increased because R, G, and B values are increased compared to the sensor not including the ionic liquids (trihexyl(tetradecyl)phosphonium bromide). Accordingly, it may be quantitatively seen that color change degree becomes greater if the ionic liquids (trihexyl(tetradecyl)phosphonium bromide) are included. Furthermore, as in the photo images of FIG. 6, it may be seen that the greatest color change degree appears if the ionic liquids (trihexyl(tetradecyl)phosphonium bromide) having optimal content (40 wt %) are included, through quantitative analysis.

[0084] FIG. 8 illustrates photo images of color change degrees obtained if the colorimetric gas sensor based on a nanofiber yarn includes ionic liquids (trihexyl(tetradecyl)phosphonium bromide) of 40 wt % and color change dyes (lead(II) acetate) of 160 wt % compared to the polymer weight, which is determined to have the most excellent color change characteristic based on the results of FIGS. 6 and 7, and those composed through the embodiment 1 were exposed to hydrogen sulfide gases of 5, 4, 3, 2 and 1 ppm for 60 seconds and if the colorimetric gas sensor based on a nanofiber yarn including only color change dyes (lead(II) acetate) of 160 wt % compared to the polymer weight, those composed through the comparative example 1 were exposed to a hydrogen sulfide gas of 1 ppm for 60, 50, 40, 30, 20, and 10 seconds.

[0085] From the photo images of FIG. 8, it may be seen that a color change degree grows greater as the hydrogen sulfide concentration increases from 1 to 5 ppm. If the exposure time was adjusted to 60, 50, 40, 30, 20, and 10 seconds at 1 ppm hydrogen sulfide concentration, it can be seen that in the color change sensors based on the nanofiber yarn including the ionic liquids (trihexyl(tetradecyl)phosphonium bromide) of 40 wt % and the color change dyes (lead(II) acetate) of 160 wt % compared to the polymer weight, color change characteristics are much excellent compared to the color change sensor based on the nanofiber yarn including only the color change dyes (lead(II) acetate) of 160 wt % compared to the polymer weight without the ionic liquids (trihexyl(tetradecyl)phosphonium bromide). If the sample not including the ionic liquids (trihexyl(tetradecyl)phosphonium bromide) was exposed to hydrogen sulfide of 1 ppm for 40 seconds or less, whether a color change is present or not is rarely determined on the photo. However, it can be seen that in the sample including the ionic liquids (trihexyl(tetradecyl)phosphonium bromide) and the sample exposed to hydrogen sulfide of 1 ppm for 20 seconds, whether a color change is present or not can be determined with the naked eye and the color change is thus excellent.

[0086] FIG. 9 is a graph quantitatively illustrating color change degrees (RGB changes) before and after exposure to hydrogen sulfide of 1 ppm for 60, 50, 40, 30, 20, and 10 seconds as in the photo images of FIG. 8. Exposure to hydrogen sulfide of 5, 4, 3, 2, and 1 ppm for 60 seconds was done for the purpose of clearer color change quantitative analysis of the color change images is illustrated in FIG. 8. As in the photo images of FIG. 8, a low level degree of color change can be seen for the case of the sensor not including the ionic liquids (trihexyl(tetradecyl)phosphonium bromide), compared to the case of the sensor including the ionic liquids (trihexyl(tetradecyl)phosphonium bromide) even through quantitative analysis. It could be seen that in the case of the sensor not including the ionic liquids (trihexyl(tetradecyl)phosphonium bromide), quantitative analysis of the color change was impossible when the sensor was exposed to hydrogen sulfide of 1 ppm for 30 seconds or less. In contrast, it could be quantitatively seen that the sensor including the ionic liquids (trihexyl(tetradecyl)phosphonium bromide) had a color change degree of at least 10 even when it was exposed to hydrogen sulfide of 1 ppm for 10 seconds. Accordingly, an excellent catalyst characteristics for the detection of hydrogen sulfide of the ionic liquids (trihexyl(tetradecyl)phosphonium bromide) can be proved.

Experimental Example 2. Evaluation of a Color Change Characteristics for Diagnosing of a Simulated Halitosis Breath Patient Using the Colorimetric Gas Sensor Based on a Complex Polymer Nanofiber Yarn for Gas Indication Including Ionic Liquids and Color Change Dyes, Composed Through the Embodiment 1

[0087] In order to evaluate the color change characteristics of the sensor to the hydrogen sulfide gas, that is known as a biomarker gas for a halitosis breath patient, a mixed gas (i.e., simulated halitosis breath patient exhaled breath) of the exhaled breath of an actual person and the hydrogen sulfide gas are fabricated. The color change characteristic is evaluated by directly exposing the color change sensors based on the nanofiber yarn including ionic liquids and color change dyes, obtained according to the embodiment 1, to the mixed gas.

[0088] After the exhaled breaths of 8 healthy persons are collected through Tedlar bags, each of the collected exhaled breaths is mixed with a hydrogen sulfide gas of a 1 ppm level. A color change degree is evaluated by directly exposing a color change sensor based on a nanofiber yarn including ionic liquids (trihexyl(tetradecyl)phosphonium bromide) of 40 wt % and color change dyes (lead(II) acetate) of 160 wt % compared to the polymer weight, which is determined to have the most excellent color change performance among the samples composed through the embodiment 1, to the mixed gas.

[0089] FIG. 10 illustrates photo images before and after simulated halitosis breath patient exhaled breaths, fabricated by mixing exhaled breaths of 8 healthy persons and hydrogen sulfide of 1 ppm, were exposed to the color change sensor based on the nanofiber yarn, including the ionic liquids (trihexyl(tetradecyl)phosphonium bromide) of 40 wt % and the color change dyes (lead(II) acetate) of 160 wt % compared to the polymer weight.

[0090] From the photos, it can be seen that the nanofiber yarn is white color before the exposure, but is brown color after the exposure of the simulated halitosis breath for 1 minute.

[0091] FIG. 11 is a graphical diagram of color change degrees (RGB changes) before and after the exposure of the simulated halitosis patient exhaled breath as in FIG. 10, for the purpose of clearer color change quantitative analysis of the color change images illustrated in FIG. 10. It can be seen that a color change occurs through a reduction of a quantitative value of a total RGB value after the exposure of the simulated halitosis patient exhaled breaths compared to the case where the simulated halitosis patient exhaled breaths were exposed. In this case, each person is different in a quantitative value of a color change because a concentration of hydrogen sulfide included in each of the 8 person exhaled breaths may be different. However, it can be seen that the color change sensor can be applied as a color change sensor capable of rapid detecting of even small amount of hydrogen sulfide gas through simulated halitosis patient exhaled breath analysis of a gas mixture of 1 ppm hydrogen sulfide gas and an exhaled breath.

[0092] Sensor characteristics of a gas sensor sensing material can be checked by taking a biomarker gas as an example through the experimental example.

[0093] By forming a colorimetric gas sensor membrane based on a nanofiber yarn for gas indication including both ionic liquids and color change dyes, the colorimetric gas sensor based on a nanofiber yarn for gas indication, in which 1) the ionic liquids having high solubility for a specific gas selectively adsorbs specific gas molecules, 2) in which it has excellent color change performance through minimum amount of color change dyes by increasing reactivity between adsorbed gas molecules and color change dyes, and 3) in which the nanofiber forms a 3-D network structure and forms an independent yarn type structure, can be fabricated.

[0094] The colorimetric gas sensor based on a complex polymer nanofiber yarn for gas indication, including ionic liquids and color change dyes in the 1-D nanofiber structure fabricated using an electro-spinning process, can have high surface area and porosity compared to the existing colorimetric gas sensor of test paper for gas detection. Accordingly, the gas sensor according to the embodiment can detect environment noxious gases (e.g., H.sub.2S, SO.sub.x, NO.sub.x or CO.sub.x) and biomarker gases (e.g., CH.sub.3COCH.sub.3, C.sub.2H.sub.5OH or C.sub.6H.sub.5CH.sub.3) included in a person's exhaled breath, with high sensitivity and high speed as it generates a color change within several tens of seconds even in the exposure to a low concentration of the gas at 1 ppm level. Furthermore, the gas sensor can be used for curved applications and fabricated in a cloth form through weaving using the structural characteristic of the independent yarn type structure.

[0095] The ionic liquids according to the embodiment can improve the adsorption property of a gas because it has high solubility for a specific gas, and can significantly improve color change sensitivity by accelerating the reaction with color change dyes. More importantly, the yarn can be easily processed, applied to surfaces having various curves, and combined with clothes through weaving because the nanofiber can be fabricated in an independent yarn type structure through a multi-electro-spinning process.

[0096] Furthermore, mass-production is easy because electro-spinning, having relatively low manufacturing cost, is used. The color change sensor according to the embodiment can generate a color change within several tens of seconds to the gas of 1 ppm level because it provides high specific surface area and porosity compared to the conventional test paper for gas detection. Therefore, the gas sensor according to the embodiment can be used for healthcare products for detecting environment noxious gases and a biomarker gas included in a person's exhaled breath.

[0097] The ionic liquids according to the embodiment can accelerate the surface chemical reaction between specific gas molecules and color change dyes by inducing the adsorption of the specific gas molecules. There can be provided the colorimetric gas sensor based on a nanofiber yarn for gas indication, in which ionic liquids and color change dyes have been functionalized and which has excellent color change performance with the least amount of dyes due to the gas molecule adsorption acceleration effect of the ionic liquids and the effective exposure of the color change dyes anchored on the high-density and high surface area nanofiber yarn scaffold.

[0098] The above description is merely a description of the technical spirit of the present invention, and those skilled in the art may change and modify the present invention in various ways without departing from the essential characteristic of the present invention. Accordingly, the embodiments disclosed in the present invention should not be construed as limiting the technical spirit of the present invention, but should be construed as illustrating the technical spirit of the present invention. The scope of the technical spirit of the present invention is not restricted by the embodiments, and the range of protection of the present invention should be interpreted based on the following appended claims. Accordingly, the range of protection of the present invention should be construed based on the following claims, and a full technological spirit within an equivalent range thereof should be construed as being included in the scope of right of the present invention.