CN100357515C - Preparation method of long-active antibacterial fiber - Google Patents

Preparation method of long-active antibacterial fiber Download PDF

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CN100357515C
CN100357515C CNB200410102295XA CN200410102295A CN100357515C CN 100357515 C CN100357515 C CN 100357515C CN B200410102295X A CNB200410102295X A CN B200410102295XA CN 200410102295 A CN200410102295 A CN 200410102295A CN 100357515 C CN100357515 C CN 100357515C
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braided fabric
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fabric
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CN1789546A (en
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林兼民
陈心杰
黄子祥
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Taiwan Textile Research Institute
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Taiwan Textile Research Institute
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Abstract

The present invention relates to a production method of long-acting antibacterial fibers. In the method, a physical vapor deposition method is utilized to form an inorganic antibacterial material with favorable adhesion properties on the surface of a fabric, and then the fabric is unwoven to obtain the antibacterial fibers. The antibacterial fibers produced by the method of the present invention have favorable wash resistance and persistent antibacterial effect, and can be woven into antibacterial fabrics with optimal softness after being mixed with other fibers.

Description

The manufacture method of long-active antibacterial fiber
Technical field
The present invention relates to a kind of manufacture method of anti-bacterial fibre, particularly have the manufacture method of the long-active antibacterial fiber of the good inorganic antibacterial material of the property followed.
Background technology
Antibiotic fabric be on fabric in conjunction with organic or inorganic antibacterial material, mainly can directly adopt anti-bacterial fibre to make each kind fabric, perhaps fabric is utilized antiseptic to carry out post processing processing to obtain anti-microbial property.Both in comparison, the former antibacterial effect is lasting, water-wash resistance is good, but the production of anti-bacterial fibre is comparatively difficult, to having relatively high expectations of antiseptic, and latter's processed is comparatively simple, washability and antibacterial effect are relatively poor.Present for want of good anti-bacterial fibre is so in various antibiotic fabrics on the market, still processing person is in the majority later on.
Except processing mode influences antibacterial effect, the more direct antiseptic that depends on of antibacterial effect.Antiseptic generally can generally be divided into the organic or inorganic antiseptic, and wherein inorganic antiseptic is applied to the antibacterial treatment of fabric in recent years gradually because of long-acting and to advantages such as the skin low irritant are low.
Prior art mainly is applied in inorganic antiseptic on the fabric in following several modes.A kind of mode is for example to utilize inorganic matter, pottery or have the ion exchangeable clay, as the silver ion carrier.Correlation technique can be with reference to No. the 6th, 514,622, United States Patent (USP) case notification number, United States Patent (USP) case notification number the 6th, 495, No. 367, United States Patent (USP) case notification number the 6th, 476, No. 095, United States Patent (USP) case notification number the 6th, 461, No. 386, United States Patent (USP) case notification number the 6th, 361, No. 567 and United States Patent (USP) case notification number the 6th, 288, No. 076, and above-mentioned patent is all classified list of references of the present invention as.
Another kind of mode then utilize macromolecule for example glue or water soluble polymer as the silver ion carrier.Correlation technique can be with reference to United States Patent (USP) case notification number the 6th, 495, No. 367, United States Patent (USP) case notification number the 6th, 238, No. 686, United States Patent (USP) case notification number the 6th, 294, No. 186, United States Patent (USP) case notification number the 6th, 264, No. 936 and United States Patent (USP) case notification number the 6th, 224, No. 898, and above-mentioned patent is also classified list of references of the present invention as.
Perhaps, can utilize the means of plating to plate antibacterial metal at material surface.Correlation technique can be with reference to No. the 6th, 267,782, No. the 6th, 451,003, United States Patent (USP) case notification number and United States Patent (USP) case notification number, and above-mentioned patent is with classifying list of references of the present invention as.
In addition, also can utilize the means of physical vapour deposition (PVD) to make the metal ultra-fine grain, to increase the dissolution rate of metal ion.Correlation technique can be with reference to No. the 5th, 985,308, No. the 6th, 333,093, United States Patent (USP) case notification number, No. the 6th, 017,553, United States Patent (USP) case notification number and United States Patent (USP) case notification number, and above-mentioned patent one is listed as list of references of the present invention.
In a word, above-mentioned prior art is not taken off in the means by various carriers, plating or physical vapour deposition (PVD) inorganic antiseptic is applied on the fabric, with problems such as the rate of release of improving inorganic antibacterial material and dissolution rates.Yet still there is following shortcoming in above-mentioned prior art.At first, with inorganic matter, pottery or have the ion exchangeable clay as the silver ion carrier, the rate of release of silver ion is lower and release time is of short duration.For above-mentioned carrier granular is disperseed in material, still need and use interfacial agent or other colloid dispersion technology, and the complexity of the process of raising.And mix and the dispersion of carrier are to belong to the leading portion process, can directly improve the difficulty of back segment process processing.
Secondly, as the silver ion carrier, be difficult for the accurately rate of release of control silver ion with macromolecule.In addition, glue or water soluble polymer might produce cytotoxicity, and polymeric additive also can harmful to human if ooze out.
Moreover, when using the means of electroplating to plate antibacterial metal, may contain harmful substance in the electroplate liquid.Add that the antibacterial metal consumption is high than other means when electroplating, but significantly do not promote antibacterial effect, cause the waste of antibacterial metal material.And, because the size of the metal coating that electroplate to form is greatly at 1 micron, easy stress or friction when the antibiotic fabric of wear electroplating processes and come off.
In addition, when utilizing the means manufacturing ultra-fine grain of physical vapour deposition (PVD), gas, pressure and the temperature etc. that need restriction to feed make the unlikely alligatoring of metal ultra-fine grain.The metal ultra-fine grain of Xing Chenging not only has the shortcoming of densely distributed and skewness because of the restriction of process thus, makes that cost is difficult for reducing, and the metal ultra-fine grain that forms easily surpasses the requirement of general clothing with antiseptic.Secondly, oppose at general suction, the good fabric of hydrophily, need expend the operation that the long period vacuumizes, with the moisture of certain removal fibrous inside because physical vapour deposition (PVD) must be finished drilling in vacuum environment.Moreover, with regard to existing equipment, and unfavorablely be plated metal ultra-fine grain on the single thread, and the design of revising or changing vacuum cavity at making anti-bacterial fibre, required cost is also high.Again, the antibiotic fabric of formation is not water-fast to be washed, rubs or bending, says nothing of in a large number and produces.
Because the bactericidal effect of silver coating fabric after suction is preferable, therefore, be necessary to provide a kind of manufacture method of long-active antibacterial fiber in fact, to overcome all weakness of above-mentioned existing process.
Summary of the invention
One of purpose of the present invention just provides a kind of manufacture method of long-active antibacterial fiber, be to utilize physical vaporous deposition to form to follow the good inorganic antibacterial material of property on the surface of braided fabric, again braided fabric is separated and be woven to anti-bacterial fibre, in order to being made into antibiotic fabric follow-up mixing with other fiber.Because the manufacture method of long-active antibacterial fiber of the present invention is effectively to control the distribution of inorganic antibacterial material with braided fabric, not only significantly reduces process cost, and good water-wash resistance and lasting antibacterial effect more are provided.Moreover long-active antibacterial fiber of the present invention can batch or the manufacturing of continous mode process.
Another object of the present invention then provides a kind of manufacture method of long acting antibiotic fabric, be to utilize physical vaporous deposition to form earlier to follow the good inorganic antibacterial material of property on the surface of braided fabric, again braided fabric is separated and be woven to anti-bacterial fibre, mix being made into antibiotic fabric then with other fiber.Thus, not only improve the pliability of existing antibiotic fabric, and good water-wash resistance and antibacterial effect is provided.
Above-mentioned purpose of the present invention can be achieved through the following technical solutions:
A kind of manufacture method of long-active antibacterial fiber is characterized in that, comprises at least:
One braided fabric is provided, and wherein this braided fabric is to be selected from a group that is made up of a circle braided fabric and a horizontal braided fabric;
Utilize a physical vaporous deposition to form an inorganic antibacterial material at least one surface of this braided fabric;
And carry out separating the process of knitting, this braided fabric is separated be woven to an anti-bacterial fibre.
Described physical vaporous deposition is to be selected from a group that is made up of sputtering method and vapour deposition method.
Described sputtering method is between 10 in the presence of blunt gas and at pressure -3Holder (Torr) is to 10 -6Carry out under one vacuum environment of holder.
Described blunt gas is to be selected from a group that is made up of nitrogen, helium, neon, argon gas and krypton gas.
Described vapour deposition method is between 10 in the presence of blunt gas and oxygen and at pressure -3Holder to 10 -6Carry out under one vacuum environment of holder.
Described blunt gas is to be selected from a group that is made up of nitrogen, helium, neon, argon gas and krypton gas.
Described physical vaporous deposition is to utilize at least one metal material one of to form target to form this inorganic antibacterial material.
Described at least one metal material is to be selected from a group that is made up of gold, silver, copper, aluminium, platinum, tantalum, bismuth, zinc and any combination thereof.
One deposition kenel of described inorganic antibacterial material is for axially to be a ultra-fine grain and a film that replaces continuously along one of this anti-bacterial fibre.
One particle diameter of described ultra-fine grain is between 1 nanometer (Nanometer; Nm) between 100 nanometers.
One surface of described anti-bacterial fibre on average has this inorganic antibacterial material between 50 percentage to 90 percentages.
Described inorganic antibacterial material is between 0.001 percentage by weight to 1 percentage by weight with respect to the average content of this anti-bacterial fibre.
The described process of knitting of separating comprises more at least:
Fix an end of this braided fabric; And
Extract a end of a thread out and this end of a thread is fixed on a yarn interwine device from the other end of this braided fabric, knit this braided fabric to obtain this anti-bacterial fibre by this yarn interwine device continuous solution.
Described separating after the process of knitting comprises more at least this anti-bacterial fibre and a fiber carried out blending with the ratio between 1: 1 to 1: 10.
Described separating after the process of knitting comprises more at least this anti-bacterial fibre and a fiber carried out blending with the ratio between 1: 1 to 1: 5.
Use the manufacture method of above-mentioned long-active antibacterial fiber and produce antibiotic fabric, owing to be to utilize physical vaporous deposition to form earlier to follow the good inorganic antibacterial material of property on the surface of braided fabric, again braided fabric is separated and be woven to anti-bacterial fibre, mix with other fiber then and be made into antibiotic fabric, therefore, not only significantly reduce process cost, improve the pliability of existing antibiotic fabric and good water-wash resistance and antibacterial effect is provided, and can realize batch or the manufacturing of continous mode process.
Description of drawings
Fig. 1 is the fabrication process flow figure of the long-active antibacterial fiber of a preferred embodiment of the present invention.
Among Fig. 1:
101: braided fabric is provided;
103: form inorganic antibacterial material at least one surface of braided fabric;
105: separate the process of knitting;
107: carry out the blending process.
The specific embodiment
The invention will be further described below in conjunction with drawings and the specific embodiments.
The manufacture method of long-active antibacterial fiber of the present invention, it is to utilize physical vaporous deposition to form to follow the good inorganic antibacterial material of property on the surface of braided fabric, braided fabric is separated be woven to anti-bacterial fibre again, in order to being made into antibiotic fabric follow-up mixing with other fiber.Below cooperate Fig. 1, describe the manufacture method of long-active antibacterial fiber of the present invention in detail.
Seeing also Fig. 1, is the fabrication process flow figure according to the long-active antibacterial fiber of a preferred embodiment of the present invention.At first, shown in step 101, provide braided fabric, wherein this braided fabric can be round braided fabric or horizontal braided fabric.Then, shown in step 103, utilize physical vaporous deposition, for example sputtering method or vapour deposition method form inorganic antibacterial material at least one surface of above-mentioned braided fabric.Furthermore, above-mentioned physical vaporous deposition is to utilize target that at least one metal material forms to carry out sputter or evaporation.According to a preferred embodiment of the present invention, above-mentioned at least one metal material is gold, silver, copper, aluminium, platinum, tantalum, bismuth, zinc or its any combination for example.In one of the present invention example, the target that can utilize fine silver for example to form, with in the presence of blunt gas and vacuum environment for example pressure between 10 -3Holder (Torr) is to 10 -6Carry out sputter between the holder.Another kind of mode, the present invention also can use the atom grain size to differ greatly the two, the target formed of the above silver of 95 percentage by weights and gold below 5 percentage by weights or platinum for example, with in the presence of blunt gas and oxygen and vacuum environment for example pressure between 10 -3Holder to 10 -6Carry out evaporation between the holder.Above-mentioned suitable blunt gas can routine nitrogen, as helium, neon, argon gas or krypton gas.Look closely the target composition of use and decide for example gold, silver, copper, aluminium, platinum, tantalum, bismuth, zinc or its any combination via the inorganic antibacterial material that aforesaid way forms.And because fiber is the influence that is woven with respect to the surfacing of target, therefore what the deposition kenel of formed inorganic antibacterial material can be along prepared anti-bacterial fibre axially is the variation that replaces continuously, for example be ultra-fine grain and film, and described ultra-fine grain and film along fiber axis to being continuously alternately.For example, be deposited on when target atom on the yarn of braided fabric amount more for a long time, the deposition kenel of formed inorganic antibacterial material is generally film.Anti-, be deposited on when target atom on the yarn of braided fabric amount more after a little while, the deposition kenel of formed inorganic antibacterial material generally is ultra-fine grain and distributes, and its particle diameter is between 1 nanometer (Nanometer; Nm) between 100 nanometers.Yet, have the knack of this skill person when understanding, physical vaporous deposition is to be used for forming inorganic antibacterial material at least one surface of above-mentioned braided fabric, also can use or in conjunction with the inorganic antibacterial material of existing other kind, therefore inorganic antibacterial material of the present invention is not limit above-mentioned and lifted.
What deserves to be mentioned is, compared to prior art is directly to form the antibacterial metal material on monofilament, owing to can't effectively control antibacterial metal material scattered band, and consumptive material consuming time, the present invention is prior to forming the then good inorganic antibacterial material of property on the surface of braided fabric, again braided fabric is separated and be woven to anti-bacterial fibre, therefore significantly reduce the material and the cost of existing process certainly.Moreover the present invention utilizes braided fabric to make anti-bacterial fibre, thus can utilize existing batch or continuous equipment manufacturing, to increase process rate.In addition, the prepared anti-bacterial fibre of the present invention, the deposition kenel that it is characterized in that inorganic antibacterial material on the long-active antibacterial fiber is ultra-fine grain and the film that replaces continuously along axially being of long-active antibacterial fiber.
After forming inorganic antibacterial material, shown in step 105, separate the process of knitting, be fixing one of braided fabric end, extract the end of a thread out and be fixed on the yarn interwine device from the other end of braided fabric again, knit braided fabric with the acquisition anti-bacterial fibre by the yarn interwine device continuous solution.According to a preferred embodiment of the present invention, surface on the anti-bacterial fibre on average has inorganic antibacterial material between 50 percentage to 90 percentages, and this inorganic antibacterial material can be between 0.001 percentage by weight to 1 percentage by weight with respect to the average content of anti-bacterial fibre.
After separating the process of knitting, more can shown in step 107, carry out the blending process, so that anti-bacterial fibre and other fiber are carried out blending, wherein to desire the kinds of fibers of blending and do not limit, end relies product demand and decides, and forms various antibiotic fabrics whereby.In addition, the ratio of anti-bacterial fibre and other various fiber blends is also decided on product demand, can for example carry out blending between 1: 1 to 1: 10 ratio, is preferable to carry out blending between 1: 1 to 1: 5 ratio so, makes the different antibiotic fabric of pliability whereby.For example, the ratio of anti-bacterial fibre blending is high more, and the antibiotic property of the antibiotic fabric of gained is preferable but hardness is harder, and is anti-, and the ratio of anti-bacterial fibre blending is low more, and the antibiotic property of the antibiotic fabric of gained is also good but soft.Via the anti-bacterial fibre of gained of the present invention and the antibiotic fabric of blending thereof, can provide good water-wash resistance and lasting antibacterial effect.Below enumerate several preferred embodiments with the more application of the manufacture method of elaboration long-active antibacterial fiber of the present invention, so it is not in order to qualification the present invention, so protection scope of the present invention is as the criterion when looking the accompanying Claim person of defining.
Embodiment 1
At first, utilize the cylinder loom, with poly terephthalic acid diethylester (Polyethylene Terephthalate; PET) yarn makes round braided fabric, and wherein the cylinder loom is that the variable pin of drum diameter 3.5 inch is counted roundlet tube loom, and PET yarn specification is false twist yarn (the Draw Textured Yarn of 75D/144F; DTY).Above-mentioned round braided fabric through close be every inch 46 orders (Mesh), and filling density is every inch 26 pins.Then, utilize the silver-colored target of purity 99.999% at flow velocity per minute 100 standard cube centimetres (Standard Cubic Centimeter Per Minute; Sccm) under argon gas exists and with about 10 -3The holder pressure carry out sputter, with the circle braided fabric dihedron Cheng Yin, wherein silver with respect to the circle braided fabric average content between 0.004 percentage by weight to 0.01 percentage by weight.
Then, silver-plated round braided fabric is separated and is knitted with the about 100 centimeters speed of knitting of separating of per minute, to obtain silver-plated PET yarn.Afterwards, silver-plated PET yarn and PET yarn carry out blending with 1: 1 ratio.Prepared antibiotic fabric can be washed and antibacterial tests.
Embodiment 2
At first, utilize the cylinder loom, the PET yarn is made round braided fabric, wherein the cylinder loom is that the variable pin of drum diameter 3.5 inch is counted roundlet tube loom, and PET yarn specification is 75D/144F DTY.Above-mentioned round braided fabric through close be every inch 46 orders, and filling density is every inch 26 pins.Then, utilize target that the platinum of the silver doping purity about 1% of purity about 99% forms in the presence of the oxygen of the argon gas of about 80 percents by volume and about 20 percents by volume and with about 10 -4The holder pressure carry out evaporation, with the circle braided fabric dihedron Cheng Yinyu platinum, wherein silver with respect to the circle braided fabric average content between 0.004 percentage by weight to 0.01 percentage by weight.
Then, the round braided fabric of silver-plated-platinum is separated and is knitted the PET yarn of-platinum silver-plated to obtain with the about 100 centimeters speed of knitting of separating of per minute.Afterwards, the PET yarn of silver-plated-platinum and PET yarn carry out blending with 1: 1 ratio.Prepared antibiotic fabric can be washed and antibacterial tests.
Embodiment 3
At first, utilize horizontal loom that the PET yarn is made horizontal braided fabric, wherein horizontal loom is the horizontal loom of 12G/ inch, and PET yarn specification is 150D/288F DTY.Above-mentioned horizontal braided fabric through close be every inch 20 orders, and filling density is every inch 16 pins.Then, utilize the silver-colored target of purity 99.999% in the presence of argon gas and with about 10 -3The holder pressure carry out sputter, with dihedron Cheng Yin at horizontal braided fabric, wherein silver with respect to the circle braided fabric average content between 0.004 percentage by weight to 0.01 percentage by weight.
Then, silver-plated horizontal braided fabric is separated and is knitted with the about 100 centimeters speed of knitting of separating of per minute, to obtain silver-plated PET yarn.Afterwards, silver-plated PET yarn and PET yarn carry out blending with 1: 1 ratio.Prepared antibiotic fabric can be washed and antibacterial tests.
Embodiment 4
At first, utilize horizontal loom that the PET yarn is made horizontal braided fabric, wherein horizontal loom is the horizontal loom of 12G/ inch, and PET yarn specification is 150D/288F DTY.Above-mentioned horizontal braided fabric through close be every inch 20 orders, and filling density is every inch 16 pins.Then, utilize target that the platinum of the silver doping purity about 1% of purity about 99% forms in the presence of the oxygen of the argon gas of about 80 percents by volume and about 20 percents by volume and with about 10 -4The pressure of holder carries out evaporation, with at the dihedron Cheng Yinyu of horizontal braided fabric platinum, wherein silver with respect to the average content of circle braided fabric between 0.004 percentage by weight to 0.01 percentage by weight.
Then, the horizontal braided fabric of silver-plated-platinum is separated and is knitted the PET yarn of-platinum silver-plated to obtain with the about 100 centimeters speed of knitting of separating of per minute.Afterwards, the PET yarn of silver-plated-platinum and PET yarn carry out blending with 1: 1 ratio.Prepared antibiotic fabric can be washed and antibacterial tests.
Embodiment 5
The antibiotic fabric that embodiment 1 to embodiment 4 makes is washed and antibacterial tests, and it is to estimate consultation (Japan Association For The Function Evaluation Of Textile according to the new function of Japanese fibre; JAFET) the antibiotic benchmark (SEK) of Zhi Dinging is assessed.At first,, no matter wash preceding or after the washing that number of times does not wait, be cut into suitable size,, inoculate quantitative test organisms and cultivate through after the sterilization treatment with the antibiotic fabric that embodiment 1 to embodiment 4 makes, wherein test organisms for example staphylococcus aureus ( Staphylococcus aureus).After cultivating 18 hours, measure uncultivated bacterium number (A) behind the inoculation bacterium liquid respectively, without the bacterium number (B) and the bacterium number (C) of antibiotic fabric after cultivating of antibiotic processing sample cloth after cultivating.With the number conversion of above-mentioned gained bacterium is logarithm value, and wherein these tests of logB-logA>1.5 expression are set up, and logA-logC shows sterilizing value, and logB-logC shows antibacterial value, and when logB-logC>2.2 represent to have bactericidal effect, and C<A represents to have fungistatic effect.And the antibiotic fabric that embodiment 1 to embodiment 4 makes is as shown in table 1 through the result of water-wash test and antibacterial tests:
Table 1
The antibiotic fabric of embodiment 1 to embodiment 4 Before the washing After washing 50 times
Antibacterial value 5.30 5.71
Sterilizing value 2.90 3.20
Even can learn that by table 1 antibiotic fabric of the present invention is through after washing 50 times, its antibacterial value and sterilizing value height are at the antibiotic benchmark of SEK and there is no remarkable change, represent that inorganic antibacterial material of the present invention is all good in the then property on the surface of different braided fabrics, and prepared antibiotic fabric can provide good water-wash resistance and lasting antibacterial effect.
In addition, the antibiotic fabric that embodiment 1 makes is washed and antibacterial tests, and it dyes chemical industry according to the U.S. and makes (the American Association Of Textile Chemists And Colorists of NAB National Association 0f Broadcasters; AATCC) the antibiotic benchmark (AATCC100-1999) of Zhi Dinging is assessed, at first, the antibiotic fabric that embodiment 1 is made, after the washing that number of times does not wait, be cut into suitable size, through after the sterilization treatment, inoculate quantitative test organisms and cultivate, wherein test organisms for example staphylococcus aureus ( Staphylococcus aureus).After cultivating 18 to 22 hours, measure behind the bacterium number (A) of antibiotic fabric after cultivating, the antibiotic fabric inoculation bacterium liquid uncultivated bacterium number (B) respectively and without the bacterium number (C) of antibiotic processing sample cloth after cultivating.Through after calculating, the result of its bacteria reducing rate is as shown in table 2 with above-mentioned gained bacterium number:
Table 2
Bacteria reducing rate (%)=100 * (B-A)/B Without antibiotic processing sample cloth Antibiotic fabric
Through washing 50 times 99.93% 99.88%
Through washing 100 times 99.93% 99.93%
Through washing 150 times 99.73% 99.46%
Through washing 200 times 99.93% 99.73%
Through washing 250 times 99.88% 98.69%
Through washing 300 times 99.93% 99.93%
Even can learn that by table 2 antibiotic fabric of the present invention is through after washing 300 times, its bacteria reducing rate still surpasses 99.90% and there is no remarkable change, reconfirm that inorganic antibacterial material of the present invention is all good in the then property on the surface of different braided fabrics, and prepared antibiotic fabric can provide good water-wash resistance and lasting antibacterial effect.
By the way be, the manufacture method of long-active antibacterial fiber provided by the present invention can be applicable to produces personal product, indoor product, medical product or motion with product etc., wherein personal product can for example keep out the cold clothing, gloves, boots, underwear, head-shield etc., indoor product is infant/old man's health care clothes, sheet, electrical blanket, quilt etc. for example, and medical product or motion product for example sufferer medical protection clothes, medicable liner, wrister, sweat shirt etc.
In brief, the manufacture method of long-active antibacterial fiber of the present invention, it is characterized in that prior to forming the then good inorganic antibacterial material of property on the surface of braided fabric, after can effectively controlling the distribution of inorganic antibacterial material by braided fabric, again braided fabric is separated and be woven to anti-bacterial fibre, in order to being made into antibiotic fabric follow-up mixing with other fiber.Thus, not only significantly reduce the cost of process, more can carry out the process that batch or continous mode are carried out long-active antibacterial fiber.
By the invention described above preferred embodiment as can be known, use the manufacture method of long-active antibacterial fiber of the present invention, its advantage is to utilize physical vaporous deposition to form and follows the good inorganic antibacterial material of property on the surface of braided fabric, again braided fabric is separated and be woven to anti-bacterial fibre, in order to being made into antibiotic fabric follow-up mixing with other fiber.Because the manufacture method of long-active antibacterial fiber of the present invention is effectively to control the distribution of inorganic antibacterial material with braided fabric, not only significantly reduces process cost, more can carry out batch or continous mode process.
By the invention described above preferred embodiment as can be known, use the manufacture method of long acting antibiotic fabric of the present invention, its advantage is to utilize physical vaporous deposition to form earlier and follows the good inorganic antibacterial material of property on the surface of braided fabric, separate again and be woven to anti-bacterial fibre, mix being made into antibiotic fabric then with other fiber.Thus, not only improve the pliability of existing antibiotic fabric, and good water-wash resistance and lasting antibacterial effect are provided.
Though the present invention provides as above with several preferred embodiments; right its is not in order to limit the present invention; anyly have the knack of this skill person; without departing from the spirit and scope of the present invention; when can being used for a variety of modifications and variations, so protection scope of the present invention is as the criterion when looking the accompanying Claim person of defining.

Claims (10)

1. the manufacture method of a long-active antibacterial fiber is characterized in that, comprises at least;
One braided fabric is provided, and wherein this braided fabric is to be selected from a group that is made up of a circle braided fabric and a horizontal braided fabric;
Utilize a physical vaporous deposition to form an inorganic antibacterial material at least one surface of this braided fabric; Wherein said physical vaporous deposition is to be selected from a group that is made up of sputtering method and vapour deposition method, and described inorganic antibacterial material is at least one metal material, and described sputtering method is between 10 in the presence of blunt gas and at pressure -3Holder to 10 -6Carry out under one vacuum environment of holder, and this pressure does not comprise 2 * 10 -4Holder; Described vapour deposition method is between 10 in the presence of blunt gas and oxygen and at pressure -3Holder to 10 -6Carry out under one vacuum environment of holder, and this pressure does not comprise 2 * 10 -4Holder;
And carry out separating the process of knitting, and this braided fabric being separated be woven to an anti-bacterial fibre, wherein said inorganic antibacterial material is between 0.001 percentage by weight to 1 percentage by weight with respect to the average content of this anti-bacterial fibre.
2. the manufacture method of long-active antibacterial fiber as claimed in claim 1 is characterized in that, described blunt gas is to be selected from a group that is made up of nitrogen, helium, neon, argon gas and krypton gas.
3. the manufacture method of long-active antibacterial fiber as claimed in claim 1 is characterized in that, described physical vaporous deposition is to utilize described at least one metal material one of to form target to form this inorganic antibacterial material.
4. the manufacture method of long-active antibacterial fiber as claimed in claim 3 is characterized in that, described at least one metal material is to be selected from a group that is made up of gold, silver, copper, aluminium, platinum, tantalum, bismuth, zinc and any combination thereof.
5. the manufacture method of long-active antibacterial fiber as claimed in claim 1, it is characterized in that, one deposition kenel of described inorganic antibacterial material is a ultra-fine grain and a film, and described ultra-fine grain and described film axially are continuously alternately along one of this anti-bacterial fibre.
6. the manufacture method of long-active antibacterial fiber as claimed in claim 5 is characterized in that, a particle diameter of described ultra-fine grain is between 1 nanometer to 100 nanometer.
7. the manufacture method of long-active antibacterial fiber as claimed in claim 1 is characterized in that, a surface of described anti-bacterial fibre on average has this inorganic antibacterial material between 50 percentage to 90 percentages.
8. the manufacture method of long-active antibacterial fiber as claimed in claim 1 is characterized in that, the described process of knitting of separating comprises more at least:
Fix an end of this braided fabric; And
Extract a end of a thread out and this end of a thread is fixed on a yarn interwine device from the other end of this braided fabric, knit this braided fabric to obtain this anti-bacterial fibre by this yarn interwine device continuous solution.
9. the manufacture method of long-active antibacterial fiber as claimed in claim 1 is characterized in that, described separating after the process of knitting comprises more at least this anti-bacterial fibre and a fiber are carried out blending with the ratio between 1: 1 to 1: 10.
10. the manufacture method of long-active antibacterial fiber as claimed in claim 1 is characterized in that, described separating after the process of knitting comprises more at least this anti-bacterial fibre and a fiber are carried out blending with the ratio between 1: 1 to 1: 5.
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WO2020065299A1 (en) 2018-09-24 2020-04-02 Splash About International Limited A garment

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