CN105239379A - Anti-static ultraviolet-proof fabric and making method thereof - Google Patents
Anti-static ultraviolet-proof fabric and making method thereof Download PDFInfo
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- CN105239379A CN105239379A CN201510777570.6A CN201510777570A CN105239379A CN 105239379 A CN105239379 A CN 105239379A CN 201510777570 A CN201510777570 A CN 201510777570A CN 105239379 A CN105239379 A CN 105239379A
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Abstract
The invention provides an anti-static ultraviolet-proof fabric and a making method thereof. Steeping liquor used for preparing the anti-static ultraviolet-proof fabric is prepared by adding, by weight, 30-40 parts of ethoxylation alkylamine, 10-15 parts of polyethylene glycol epoxy glycerin ether, 10-20 parts of tetrabutyl titanate, 5-15 parts of surfactants, 5-15 parts of zinc acetate, 15-25 parts of ethylene glycol, 25-35 parts of glycerin, 10-15 parts of phenyl salicytate and 10-15 parts of sulfated glycine betaine into a coupling agent and a dispersing agent and stirring the mixture. The fabric has the good anti-static ultraviolet-proof effects and is washable, less in influence on the fabric handfeel and free of harm to the skins.
Description
Technical field
The invention belongs to textile material field, particularly relate to a kind of Antistatic anti-ultraviolet wire fabric and preparation method thereof.
Background technology
Along with the progress of science and technology, people's living standard is improved, and everybody is also more and more higher to the requirement of textiles, dacron due to have powerful high, WATER REPELLENCY good, soft, dark liking by consumers in general.But dacron in use often fluffs, balling-up, affects aesthetic feeling and the wearability of outward appearance.Reason and the fiber trait of the easy balling-up of dacron are closely related, mainly between fiber, cohesive force intensity that is little, fiber is high, ability of extending is large, particularly resist bending fatigue, resistance to torsional fatigue and ABRASION RESISTANCE are good, therefore fiber easily skids off fabric face, make the fiber of fabric face be exposed to fabric, present a lot of young pilose antler at fabric face, if these young pilose antlers can not come off in time, with regard to mutual tied up in knots, be kneaded into many spherical granules, be commonly referred to balling-up.
Ultraviolet skin ambustion in recent years, adds the probability that people suffer from cutaneum carcinoma, even if use sun-proof articles; but the region of protection is also limited, and therefore, people wish that textiles can meet different demands in different environments; research and development multifunctional fabric, to meet people's life and work needs.
Summary of the invention
In order to overcome deficiency of the prior art, the invention provides a kind of Antistatic anti-ultraviolet wire fabric and preparation method thereof, fabric antistatic effect prepared by the present invention is good, and has the function of antiultraviolet simultaneously, to meet the needs of multiple occasion in people's life and work.
For solving the problems of the technologies described above, the technical solution used in the present invention is as follows:
First aspect, the invention provides a kind of Antistatic anti-ultraviolet wire fabric, and the preparation method of described Antistatic anti-ultraviolet wire fabric comprises the steps:
(1) following raw material is taken by weight: the sulfatobetaine of the zinc acetate of the tetrabutyl titanate of the ethoxylated alkylamine of 30-40 weight portion, the polyethylene glycol Synthesis of Oligo Ethylene Glycol of 10-15 weight portion, 10-20 weight portion, the surfactant of 5-15 weight portion, 5-15 weight portion, the ethylene glycol of 15-25 weight portion, the glycerine of 25-35 weight portion, the phenyl salicytate of 10-15 weight portion and 10-15 weight portion;
(2) ethoxylated alkylamine taken, polyethylene glycol Synthesis of Oligo Ethylene Glycol, tetrabutyl titanate, surfactant, zinc acetate, ethylene glycol, glycerine, phenyl salicytate and sulfate beet are mixed, add coupling agent and dispersant, continue to stir, prepare maceration extract;
(3) carry out soaking and rolling operation in maceration extract fabric prepared in step (2);
(4) it is dry that the fabric after step (3) being processed is placed in baking oven, prepares described Antistatic anti-ultraviolet wire fabric.
In the present invention, the consumption of described ethoxylated alkylamine is 30-40 weight portion, such as 30 weight portions, 31 weight portions, 32 weight portions, 33 weight portions, 34 weight portions, 35 weight portions, 36 weight portions, 37 weight portions, 38 weight portions, 39 weight portions or 40 weight portions.
Ethoxylated alkylamine of the present invention is effectively antistatic additive, even as the same at low relative humidity, and also permanently effective.The approval of this kind of antistatic additive Yi Huo federal food drug and cosmetic act Drug Administration, is applied in the article with indirect food contact.
In the present invention, the consumption of described polyethylene glycol Synthesis of Oligo Ethylene Glycol is 10-15 weight portion, such as 10 weight portions, 11 weight portions, 12 weight portions, 13 weight portions, 14 weight portions or 15 weight portions.
In the present invention, the consumption of described tetrabutyl titanate is 10-20 weight portion, such as 10 weight portions, 11 weight portions, 12 weight portions, 13 weight portions, 14 weight portions, 15 weight portions, 16 weight portions, 17 weight portions, 18 weight portions, 19 weight portions or 20 weight portions.
In the present invention, the consumption of described surfactant is 5-15 weight portion, such as 5 weight portions, 6 weight portions, 7 weight portions, 8 weight portions, 9 weight portions, 10 weight portions, 11 weight portions, 12 weight portions, 13 weight portions, 14 weight portions or 15 weight portions.
In the present invention, the consumption of described zinc acetate is 5-15 weight portion, such as 5 weight portions, 6 weight portions, 7 weight portions, 8 weight portions, 9 weight portions, 10 weight portions, 11 weight portions, 12 weight portions, 13 weight portions, 14 weight portions or 15 weight portions.
In the present invention, the consumption of described ethylene glycol is 15-25 weight portion, such as 15 weight portions, 16 weight portions, 17 weight portions, 18 weight portions, 19 weight portions, 20 weight portions, 21 weight portions, 22 weight portions, 23 weight portions, 24 weight portions or 25 weight portions.
In the present invention, the consumption of described glycerine is 25-35 weight portion, such as 25 weight portions, 26 weight portions, 27 weight portions, 28 weight portions, 29 weight portions, 30 weight portions, 31 weight portions, 32 weight portions, 33 weight portions, 34 weight portions or 35 weight portions.
In the present invention, the consumption of described phenyl salicytate is 10-15 weight portion, such as 10 weight portions, 11 weight portions, 12 weight portions, 13 weight portions, 14 weight portions or 15 weight portions.
Phenyl salicytate of the present invention has good anti-ultraviolet function.
In the present invention, the consumption of described sulfatobetaine is 10-15 weight portion, such as 10 weight portions, 11 weight portions, 12 weight portions, 13 weight portions, 14 weight portions or 15 weight portions.
Sulfatobetaine of the present invention is a kind of well antistatic agent.
In the present invention, step (2) described coupling agent is silane coupler.
In the present invention, step (2) described dispersant is Sodium Polyacrylate.
Preferably, the viscosity of described dispersant is 200-280mPas, such as 200mPas, 205mPas, 210mPas, 215mPas, 220mPas, 225mPas, 230mPas, 235mPas, 240mPas, 245mPas, 250mPas, 255mPas, 260mPas, 265mPas, 270mPasmPas, 275mPas or 280mPas etc., be preferably 240-260mPas.
In the present invention, step (2) described mixing time is 35-50min, such as 35min, 36min, 37min, 38min, 39min, 40min, 41min, 42min, 43min, 44min, 45min, 46min, 47min, 48min, 49min or 50min etc., be preferably 40-45min.
In the present invention, described in step (2), the mass concentration of maceration extract is 30%-40%, such as 30%, 31%, 32%, 32%, 33%, 34%, 35%, 36%, 37%, 38%, 39% or 40% etc., pH value is 5-7, such as 5,6 or 7 etc.
In the present invention, a leaching one described in step (3) rolls circulation 2-4 time, such as 2 times, 3 times or 4 times, is preferably 3 times.
In the present invention, a leaching one described in step (3) rolls circulation repeatedly, and fabric can be made to obtain the function of Antistatic anti-ultraviolet line better.
In the present invention, the pressure rolled described in step (3) is 1.5kg/cm
2, 1.6kg/cm
2, 1.7kg/cm
2, 1.8kg/cm
2, 1.9kg/cm
2, 2.0kg/cm
2, 2.1kg/cm
2or 2.2kg/cm
2deng, pick-up rate is 30-60%, such as 30%, 32%, 34%, 36%, 38%, 40%, 42%, 44%, 46%, 48%, 50%, 52%, 54%, 56%, 58% or 60% etc.
In the present invention, temperature dry described in step (4) is 140-160 DEG C, such as 140 DEG C, 141 DEG C, 142 DEG C, 142 DEG C, 143 DEG C, 144 DEG C, 145 DEG C, 146 DEG C, 147 DEG C, 148 DEG C, 149 DEG C, 150 DEG C, 151 DEG C, 152 DEG C, 153 DEG C, 154 DEG C, 155 DEG C, 156 DEG C, 157 DEG C, 158 DEG C, 159 DEG C or 160 DEG C etc., time is 1.5-3h, such as 1.5h, 1.6h, 1.7h, 1.8h, 1.9h, 2.0h, 2.1h, 2.2h, 2.3h, 2.4h, 2.5h, 2.6h, 2.7h, 2.8h, 2.9h or 3h etc.
As the preferred technical solution of the present invention, the preparation method of described Antistatic anti-ultraviolet wire fabric comprises the steps:
(1) following raw material is taken by weight: the sulfatobetaine of the zinc acetate of the tetrabutyl titanate of the ethoxylated alkylamine of 30-40 weight portion, the polyethylene glycol Synthesis of Oligo Ethylene Glycol of 10-15 weight portion, 10-20 weight portion, the surfactant of 5-15 weight portion, 5-15 weight portion, the ethylene glycol of 15-25 weight portion, the glycerine of 25-35 weight portion, the phenyl salicytate of 10-15 weight portion and 10-15 weight portion;
(2) ethoxylated alkylamine taken, polyethylene glycol Synthesis of Oligo Ethylene Glycol, tetrabutyl titanate, surfactant, zinc acetate, ethylene glycol, glycerine, phenyl salicytate and sulfate beet are mixed, add silane coupler and sodium polyacrylate disperant, continue to stir 35-50min, prepare that mass concentration is 30%-40%, pH value is the maceration extract of 5-7;
(3) carry out soaking and rolling operation, circulation 2-4 time in maceration extract fabric prepared in step (2);
(4) fabric after step (3) being processed is placed in baking oven at 140-160 DEG C of dry 1.5-3h, prepares described Antistatic anti-ultraviolet wire fabric.
Compared with prior art, the present invention has following beneficial effect:
Fabric of the present invention has good Antistatic anti-ultraviolet line function, and water-fastness, simultaneously less on fabric feeling impact, to skin fanout free region.
Detailed description of the invention
For better the present invention being described, be convenient to understand technical scheme of the present invention, below the present invention is described in more detail.But following embodiment is only simple and easy example of the present invention, and do not represent or limit the scope of the present invention, scope is as the criterion with claims.
Embodiment 1
The present embodiment Antistatic anti-ultraviolet wire fabric is prepared by following step:
(1) following raw material is taken by weight: the sulfatobetaine of the zinc acetate of the tetrabutyl titanate of the ethoxylated alkylamine of 30 weight portions, the polyethylene glycol Synthesis of Oligo Ethylene Glycol of 15 weight portions, 20 weight portions, the surfactant of 15 weight portions, 15 weight portions, the ethylene glycol of 25 weight portions, the glycerine of 35 weight portions, the phenyl salicytate of 10 and 10 weight portions;
(2) ethoxylated alkylamine taken, polyethylene glycol Synthesis of Oligo Ethylene Glycol, tetrabutyl titanate, surfactant, zinc acetate, ethylene glycol, glycerine, phenyl salicytate and sulfate beet are mixed, add silane coupler and sodium polyacrylate disperant, the viscosity of dispersant is 200mPas, continue to stir 35min, prepare that mass concentration is 30%, pH value is the maceration extract of 5;
(3) in the maceration extract prepared in step (2) by fabric, a leaching one is rolled, described in the pressure that rolls be 1.5kg/cm
2pressure under roll, pick-up rate is 30%, circulates 2 times;
(4) fabric after step (3) being processed is placed in baking oven at 140 DEG C of dry 3h, prepares described Antistatic anti-ultraviolet wire fabric.
Embodiment 2
The present embodiment Antistatic anti-ultraviolet wire fabric is prepared by following step:
(1) following raw material is taken by weight: the sulfatobetaine of the zinc acetate of the tetrabutyl titanate of the ethoxylated alkylamine of 40 weight portions, the polyethylene glycol Synthesis of Oligo Ethylene Glycol of 10 weight portions, 10 weight portions, the surfactant of 5 weight portions, 5 weight portions, the ethylene glycol of 15 weight portions, the glycerine of 25 weight portions, the phenyl salicytate of 15 and 15 weight portions;
(2) ethoxylated alkylamine taken, polyethylene glycol Synthesis of Oligo Ethylene Glycol, tetrabutyl titanate, surfactant, zinc acetate, ethylene glycol, glycerine, phenyl salicytate and sulfate beet are mixed, add silane coupler and sodium polyacrylate disperant, the viscosity of dispersant is 280mPas, continue to stir 50min, prepare that mass concentration is 40%, pH value is the maceration extract of 7;
(3) in the maceration extract prepared in step (2) by fabric, a leaching one is rolled, described in the pressure that rolls be 2.2kg/cm
2pressure under roll, pick-up rate is 60%, circulates 4 times;
(4) fabric after step (3) being processed is placed in baking oven at 160 DEG C of dry 1.5h, prepares described Antistatic anti-ultraviolet wire fabric.
Embodiment 3
The present embodiment Antistatic anti-ultraviolet wire fabric is prepared by following step:
(1) following raw material is taken by weight: the sulfatobetaine of the zinc acetate of the tetrabutyl titanate of the ethoxylated alkylamine of 35 weight portions, the polyethylene glycol Synthesis of Oligo Ethylene Glycol of 13 weight portions, 15 weight portions, the surfactant of 10 weight portions, 10 weight portions, the ethylene glycol of 20 weight portions, the glycerine of 30 weight portions, the phenyl salicytate of 12 and 13 weight portions;
(2) ethoxylated alkylamine taken, polyethylene glycol Synthesis of Oligo Ethylene Glycol, tetrabutyl titanate, surfactant, zinc acetate, ethylene glycol, glycerine, phenyl salicytate and sulfate beet are mixed, add silane coupler and sodium polyacrylate disperant, the viscosity of dispersant is 240mPas, continue to stir 33min, prepare that mass concentration is 35%, pH value is the maceration extract of 6;
(3) in the maceration extract prepared in step (2) by fabric, a leaching one is rolled, described in the pressure that rolls be 2.0kg/cm
2pressure under roll, pick-up rate is 45%, circulates 3 times;
(4) fabric after step (3) being processed is placed in baking oven at 150 DEG C of dry 2h, prepares described Antistatic anti-ultraviolet wire fabric.
Comparative example 1
The difference of this comparative example and embodiment 1 is only to prepare in the raw material of Antistatic anti-ultraviolet wire fabric and does not comprise phenyl salicytate, all the other raw materials and raw material dosage and preparation method all identical with embodiment 1 with condition.
Comparative example 2
The difference of this comparative example and embodiment 1 is only to prepare in the raw material of Antistatic anti-ultraviolet wire fabric and does not comprise ethoxylated alkylamine and sulfatobetaine, all the other raw materials and raw material dosage and preparation method all identical with embodiment 1 with condition.
Comparative example 3
The difference of this comparative example and embodiment 1 is only to prepare in the raw material of Antistatic anti-ultraviolet wire fabric and does not comprise ethoxylated alkylamine, all the other raw materials and raw material dosage and preparation method all identical with embodiment 1 with condition.
Comparative example 4
The difference of this comparative example and embodiment 1 is only to prepare in the raw material of Antistatic anti-ultraviolet wire fabric and does not comprise sulfatobetaine, all the other raw materials and raw material dosage and preparation method all identical with embodiment 1 with condition.
Comparative example 5
The difference of this comparative example and embodiment 1 is only to prepare in the raw material of Antistatic anti-ultraviolet wire fabric and does not comprise ethoxylated alkylamine, and the consumption of sulfatobetaine is 20 weight portions, all the other raw materials and raw material dosage and preparation method all identical with embodiment 1 with condition.
Comparative example 6
The difference of this comparative example and embodiment 1 is only to prepare in the raw material of Antistatic anti-ultraviolet wire fabric and does not comprise sulfatobetaine, and the consumption of ethoxylated alkylamine is 20 weight portions, all the other raw materials and raw material dosage and preparation method all identical with embodiment 1 with condition.
Comparative example 7
The consumption that the difference of this comparative example and embodiment 1 is only to prepare polyethylene glycol Synthesis of Oligo Ethylene Glycol in the raw material of Antistatic anti-ultraviolet wire fabric is 20 weight portions, all the other raw materials and raw material dosage and preparation method all identical with embodiment 1 with condition.
Comparative example 8
The consumption that the difference of this comparative example and embodiment 1 is only to prepare tetrabutyl titanate in the raw material of Antistatic anti-ultraviolet wire fabric is 25 weight portions, all the other raw materials and raw material dosage and preparation method all identical with embodiment 1 with condition.
Comparative example 9
The consumption that the difference of this comparative example and embodiment 1 is only to prepare zinc acetate in the raw material of Antistatic anti-ultraviolet wire fabric is 20 weight portions, all the other raw materials and raw material dosage and preparation method all identical with embodiment 1 with condition.
Comparative example 10
The consumption that the difference of this comparative example and embodiment 1 is only to prepare glycerine in the raw material of Antistatic anti-ultraviolet wire fabric is 20 weight portions, all the other raw materials and raw material dosage and preparation method all identical with embodiment 1 with condition.
Carry out antiultraviolet after fabric washing prepared by the fabric prepare embodiment 1-3 and comparative example 1-10 50 times and antistatic property detects, detection method used is with reference to national standard, and measurement result is as shown in table 1:
Table 1
Antiultraviolet (UPF) | Electrostatic pressure (V) | |
Embodiment 1 | 56 | 613 |
Embodiment 2 | 60 | 580 |
Embodiment 3 | 58 | 599 |
Comparative example 1 | 10 | 641 |
Comparative example 2 | 54 | 1103 |
Comparative example 3 | 55 | 790 |
Comparative example 4 | 54 | 810 |
Comparative example 5 | 53 | 760 |
Comparative example 6 | 54 | 866 |
Comparative example 7 | 54 | 650 |
Comparative example 8 | 52 | 661 |
Comparative example 9 | 53 | 670 |
Comparative example 10 | 54 | 674 |
The result of integrated embodiment 1-3 can be found out, still have higher uvioresistant and the performance of antistatic after the fabric washing that the present invention prepares 50 times, water-wash resistance is good.In comparative example 1, do not comprise phenyl salicytate in raw materials, under the preparation condition identical with embodiment 1, prepare the performance of fabric not as the present invention's preparation, especially the performance of antiultraviolet obviously declines.This is main because the present invention's phenyl salicytate used has well absorb ultraviolet function.
Ethoxylated alkylamine and sulfatobetaine is not comprised in raw materials in comparative example 2, the antistatic property preparing fabric obviously declines, ethoxylated alkylamine is not comprised in raw materials in comparative example 3, sulfatobetaine is not comprised in raw materials in comparative example 4, compared with comparative example 2, the antistatic property preparing fabric obviously improves, but all not as fabric prepared by the present invention.This illustrate ethoxylated alkylamine and sulfatobetaine strengthen fabric antistatic in there is synergy.
In addition, fabric prepared by the present invention wants the antistatic and ultraviolet resistance obtained, organic cooperation is needed between each composition, when in the raw material preparing Antistatic anti-ultraviolet wire fabric, when the content of certain or some component is not in limited range of the present invention, can have an impact to the performance of fabric, such as comparative example 5-10, because the content of certain or some component exceeds limited range of the present invention, cause the antistatic of fabric and ultraviolet resistance all not as fabric prepared by the present invention.
Applicant states, the present invention illustrates a kind of Antistatic anti-ultraviolet wire fabric of the present invention and preparation method thereof by above-described embodiment, but the present invention is not limited to above-described embodiment, does not namely mean that the present invention must rely on above-described embodiment and could implement.Person of ordinary skill in the field should understand, any improvement in the present invention, to equivalence replacement and the interpolation of auxiliary element, the concrete way choice etc. of each raw material of product of the present invention, all drops within protection scope of the present invention and open scope.
Claims (10)
1. an Antistatic anti-ultraviolet wire fabric, is characterized in that, the preparation method of described Antistatic anti-ultraviolet wire fabric comprises the steps:
(1) following raw material is taken by weight: the sulfatobetaine of the zinc acetate of the tetrabutyl titanate of the ethoxylated alkylamine of 30-40 weight portion, the polyethylene glycol Synthesis of Oligo Ethylene Glycol of 10-15 weight portion, 10-20 weight portion, the surfactant of 5-15 weight portion, 5-15 weight portion, the ethylene glycol of 15-25 weight portion, the glycerine of 25-35 weight portion, the phenyl salicytate of 10-15 weight portion and 10-15 weight portion;
(2) ethoxylated alkylamine taken, polyethylene glycol Synthesis of Oligo Ethylene Glycol, tetrabutyl titanate, surfactant, zinc acetate, ethylene glycol, glycerine, phenyl salicytate and sulfate beet are mixed, add coupling agent and dispersant, continue to stir, prepare maceration extract;
(3) in the maceration extract prepared in step (2) by fabric, a leaching one is rolled;
(4) it is dry that the fabric after step (3) being processed is placed in baking oven, prepares described Antistatic anti-ultraviolet wire fabric.
2. Antistatic anti-ultraviolet wire fabric according to claim 1, it is characterized in that, described in step (2), coupling agent is silane coupler.
3. Antistatic anti-ultraviolet wire fabric according to claim 1, it is characterized in that, described in step (2), dispersant is Sodium Polyacrylate;
Preferably, described dispersant viscosity is 200-280mPas, is preferably 240-260mPas.
4. Antistatic anti-ultraviolet wire fabric according to claim 1, it is characterized in that, described in step (2), mixing time is 35-50min, is preferably 40-45min.
5. Antistatic anti-ultraviolet wire fabric according to claim 1, it is characterized in that, described in step (2), the mass concentration of maceration extract is 30%-40%, and pH value is 5-7.
6. Antistatic anti-ultraviolet wire fabric according to claim 1, is characterized in that, circulation 2-4 time is rolled in a leaching one described in step (3), preferably 3 times.
7. Antistatic anti-ultraviolet wire fabric according to claim 1, it is characterized in that, the pressure rolled described in step (3) is 1.5-2.2kg/cm
2, pick-up rate is 30-60%.
8. Antistatic anti-ultraviolet wire fabric according to claim 1, is characterized in that, temperature dry described in step (4) is 140-160 DEG C, and the time is 1.5-3h.
9. Antistatic anti-ultraviolet wire fabric according to any one of claim 1-8, is characterized in that, the preparation method of described Antistatic anti-ultraviolet wire fabric comprises the steps:
(1) following raw material is taken by weight: the sulfatobetaine of the zinc acetate of the tetrabutyl titanate of the ethoxylated alkylamine of 30-40 weight portion, the polyethylene glycol Synthesis of Oligo Ethylene Glycol of 10-15 weight portion, 10-20 weight portion, the surfactant of 5-15 weight portion, 5-15 weight portion, the ethylene glycol of 15-25 weight portion, the glycerine of 25-35 weight portion, the phenyl salicytate of 10-15 weight portion and 10-15 weight portion;
(2) ethoxylated alkylamine taken, polyethylene glycol Synthesis of Oligo Ethylene Glycol, tetrabutyl titanate, surfactant, zinc acetate, ethylene glycol, glycerine, phenyl salicytate and sulfate beet are mixed, add silane coupler and sodium polyacrylate disperant, continue to stir 35-50min, prepare that mass concentration is 30%-40%, pH value is the maceration extract of 5-7;
(3) carry out soaking and rolling operation, circulation 2-4 time in maceration extract fabric prepared in step (2);
(4) fabric after step (3) being processed is placed in baking oven at 140-160 DEG C of dry 1.5-3h, prepares described Antistatic anti-ultraviolet wire fabric.
10. the Antistatic anti-ultraviolet wire fabric that method prepares according to any one of claim 1-9.
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Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
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CN106005531A (en) * | 2016-07-06 | 2016-10-12 | 成都格虹电子科技有限责任公司 | Cover tape heat-sealing process method |
CN106012509A (en) * | 2016-07-29 | 2016-10-12 | 芜湖华烨工业用布有限公司 | Preparation method of antistatic cotton fabric |
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CN107663769A (en) * | 2017-11-13 | 2018-02-06 | 安徽创荣服装辅料有限公司 | A kind of garment lining antistatic additive |
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102851975A (en) * | 2012-09-10 | 2013-01-02 | 昆山市周市惠宏服装厂 | Antistatic fabric and production method thereof |
CN103790026A (en) * | 2014-01-24 | 2014-05-14 | 南通惠通纺织器材有限公司 | Neatening method of ultraviolet-proof antistatic fabric |
CN104294582A (en) * | 2014-09-25 | 2015-01-21 | 苏州印丝特纺织数码科技有限公司 | Preparation method of anti-ultraviolet finishing agent for silk fabric |
CN104878597A (en) * | 2015-06-12 | 2015-09-02 | 张萍 | Fabric antistatic agent |
-
2015
- 2015-11-14 CN CN201510777570.6A patent/CN105239379A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102851975A (en) * | 2012-09-10 | 2013-01-02 | 昆山市周市惠宏服装厂 | Antistatic fabric and production method thereof |
CN103790026A (en) * | 2014-01-24 | 2014-05-14 | 南通惠通纺织器材有限公司 | Neatening method of ultraviolet-proof antistatic fabric |
CN104294582A (en) * | 2014-09-25 | 2015-01-21 | 苏州印丝特纺织数码科技有限公司 | Preparation method of anti-ultraviolet finishing agent for silk fabric |
CN104878597A (en) * | 2015-06-12 | 2015-09-02 | 张萍 | Fabric antistatic agent |
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CN106005531A (en) * | 2016-07-06 | 2016-10-12 | 成都格虹电子科技有限责任公司 | Cover tape heat-sealing process method |
CN106012509A (en) * | 2016-07-29 | 2016-10-12 | 芜湖华烨工业用布有限公司 | Preparation method of antistatic cotton fabric |
CN106987096A (en) * | 2017-05-19 | 2017-07-28 | 汪建军 | A kind of building energy conservation fiber glass resin |
CN107663769A (en) * | 2017-11-13 | 2018-02-06 | 安徽创荣服装辅料有限公司 | A kind of garment lining antistatic additive |
CN108071013A (en) * | 2017-11-30 | 2018-05-25 | 安徽宏远无纺布业有限公司 | A kind of cloth antistatic agent |
CN110558685A (en) * | 2019-09-10 | 2019-12-13 | 健力粘扣带有限公司 | manufacturing method of anti-static water-resistant hot-melting nylon fastening tape |
CN110699818A (en) * | 2019-10-16 | 2020-01-17 | 南通绿芭蕉纺织品有限公司 | Fabric with good radiation protection effect |
CN114635281A (en) * | 2022-04-25 | 2022-06-17 | 吴江市兰天织造有限公司 | Terylene weft elastic wave crepe double-layer down-filled cloth |
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