CN1760440A - Nano antistatic finishing agent, preparation method and application - Google Patents
Nano antistatic finishing agent, preparation method and application Download PDFInfo
- Publication number
- CN1760440A CN1760440A CN 200510117126 CN200510117126A CN1760440A CN 1760440 A CN1760440 A CN 1760440A CN 200510117126 CN200510117126 CN 200510117126 CN 200510117126 A CN200510117126 A CN 200510117126A CN 1760440 A CN1760440 A CN 1760440A
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- CN
- China
- Prior art keywords
- finishing agent
- weight
- alumina sol
- isopropyl alcohol
- aluminium isopropoxide
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
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- 238000002360 preparation method Methods 0.000 title claims abstract description 15
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 55
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims abstract description 42
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 99
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 46
- SMZOGRDCAXLAAR-UHFFFAOYSA-N aluminium isopropoxide Chemical compound [Al+3].CC(C)[O-].CC(C)[O-].CC(C)[O-] SMZOGRDCAXLAAR-UHFFFAOYSA-N 0.000 claims description 33
- 238000003756 stirring Methods 0.000 claims description 28
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 18
- 229920004933 Terylene® Polymers 0.000 claims description 16
- 239000004094 surface-active agent Substances 0.000 claims description 15
- 239000004744 fabric Substances 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 230000032683 aging Effects 0.000 claims description 11
- 239000008367 deionised water Substances 0.000 claims description 11
- 229910021641 deionized water Inorganic materials 0.000 claims description 11
- 239000002244 precipitate Substances 0.000 claims description 11
- 239000013049 sediment Substances 0.000 claims description 11
- 238000010792 warming Methods 0.000 claims description 11
- 239000006184 cosolvent Substances 0.000 claims description 6
- -1 polyoxyethylene Polymers 0.000 claims description 6
- 239000000835 fiber Substances 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 229920000728 polyester Polymers 0.000 claims description 4
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 3
- 229920002972 Acrylic fiber Polymers 0.000 claims description 2
- 239000004952 Polyamide Substances 0.000 claims description 2
- 239000004743 Polypropylene Substances 0.000 claims description 2
- 229920002647 polyamide Polymers 0.000 claims description 2
- 229920001155 polypropylene Polymers 0.000 claims description 2
- 230000000694 effects Effects 0.000 abstract description 4
- 229910010272 inorganic material Inorganic materials 0.000 abstract description 2
- 239000011147 inorganic material Substances 0.000 abstract description 2
- 239000002736 nonionic surfactant Substances 0.000 abstract 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 12
- 229920002451 polyvinyl alcohol Polymers 0.000 description 12
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 6
- 229910052782 aluminium Inorganic materials 0.000 description 6
- 239000004411 aluminium Substances 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 239000004753 textile Substances 0.000 description 6
- 239000000654 additive Substances 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229920004934 Dacron® Polymers 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- 238000005034 decoration Methods 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 206010013786 Dry skin Diseases 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000413 hydrolysate Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 238000005213 imbibition Methods 0.000 description 1
- 150000002462 imidazolines Chemical class 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229940051841 polyoxyethylene ether Drugs 0.000 description 1
- 229920000056 polyoxyethylene ether Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
The present invention discloses a nano antistatic finishing agent, its preparation method and application. The described finishing agent contains alumina sol, PVA whose content is 0.1-0.5 wt% of alumina sol weight and non-ionic surfactant whose content is 0.1-1 wt% of alumina sol weight. Said invention adopts nano-size inorganic material, so that it can obtain good antistatic effect.
Description
One, technical field:
The present invention relates to a kind of fabrics antistatic agent finishing agent and its production and application, especially relate to a kind of nano antistatic finishing agent and its production and application.
Two, background technology:
Synthetic fiber such as terylene are hydrophobic synthetic fibre, and water imbibition is poor, in use, because of friction produces static, cause that dust adheres to, and make terylene clothes tangle limbs and produce the adhesion sense of discomfort, even be harmful to healthy.While because terylene etc. is a flammable fiber, and the burning of clothes such as terylene may cause the human injury, and the burning of drapery can cause fire such as building, automobile or aircraft.So it is necessary that clothes, drapery are carried out antistatic finish.
Reach the anlistatig purpose of textiles, the most common way is that the used for textiles antistatic additive is put in order in the prior art.To the arrangement of used for textiles antistatic additive, respond well, simple to operate, practical, be widely adopted.Present widely used antistatic additive is many to be the finishing agent of main component preparation with organic substances such as quaternary ammonium salt, esters of acrylic acid, imidazolines.This class finishing agent short run effect is better, but washability is relatively poor, easily cause the fabric color ligh modification.
Three, summary of the invention:
One of purpose of the present invention provides a kind of nanometer finishing agent with antistatic property.
Two of purpose of the present invention provides the preparation method of this nano antistatic finishing agent.
Three of purpose of the present invention provides and adopts the application of above-mentioned nano antistatic finishing agent on textiles.
These and other purpose of the present invention will further embody and set forth by following detailed description and explanation.
The preparation method's of nano antistatic finishing agent of the present invention feature is under certain condition, adopts organic aluminium alcoholates hydrolysis to make aluminium colloidal sol, and the technique for applying range of choice at the terylene textiles is provided.
According to above feature, the implementation step of nano-anti static agent preparation of the present invention is:
1, organic aluminium alcoholates hydrolysis;
2, organic aluminium alcoholates hydrolysate polycondensation;
3, inorganic acid or mixed acid depolymerization;
4, obtain aluminium colloidal sol (can be transparent or semitransparent);
A kind of nano antistatic finishing agent that in aluminium colloidal sol, adds the PVA account for alumina sol weight 0.1-0.5% (weight) and 0.1-1% (weight) non-ionic surface active agent such as alkylphenol polyoxyethylene, OP-10 or TX-10 and make.
Nano antistatic finishing agent of the present invention contains alumina sol.Further, also contain in the PVA of alumina sol 0.1-0.5 weight % and the non-ionic surface active agent of 0.1-1 weight %.Be preferably in the PVA of alumina sol 0.2-0.4 weight % with in the non-ionic surface active agent of alumina sol 0.3-0.7 weight %.More preferably in the PVA of alumina sol 0.3 weight % with in the non-ionic surface active agent of alumina sol 0.5 weight %.
In nano antistatic finishing agent of the present invention, described alumina sol obtains by the following method: deionized water is heated to 75-85 ℃ of temperature, the aluminium isopropoxide gradation that to dissolve with isopropyl alcohol while stirring behind the constant temperature slowly adds, wherein the molar ratio of aluminium isopropoxide and isopropyl alcohol is 1: 1-3, all add the back backflow and stirred 1-2 hour, form white precipitate.Be warming up to 90-100 ℃ again, after the stirring condition lower open mouth is evaporated to isopropyl alcohol and volatilizees fully, press aluminium isopropoxide: the amount of the mol ratio 1 of hydrochloric acid: 0.1-0.3 adds peptizing agent hydrochloric acid, and sediment is disperseed again, ageing 3-5 hour, transparent alumina colloidal sol.
The preparation method of nano antistatic finishing agent of the present invention, concrete steps are as follows:
Earlier deionized water is heated to 75-85 ℃ of temperature, the aluminium isopropoxide gradation that to dissolve with the cosolvent isopropyl alcohol while stirring behind the constant temperature slowly adds, wherein the molar ratio of aluminium isopropoxide and isopropyl alcohol is 1: 1-3, and all add the back backflow and stirred 1-2 hour, form white precipitate.Be warming up to 90-100 ℃ again, the stirring condition lower open mouth be evaporated to produce isopropyl alcohol and volatilize fully after, press aluminium isopropoxide: the mol ratio 1 of hydrochloric acid: 0.1-0.3 adds peptizing agent hydrochloric acid, and sediment is disperseed again, ageing 3-5 hour, must transparent alumina colloidal sol; In alumina sol, add then and account for the PVA of alumina sol total amount 0.1-0.5 weight % and the non-ionic surface active agent of 0.1-1 weight % makes nano antistatic finishing agent.
Further, the preparation method of nano antistatic finishing agent of the present invention, concrete steps are as follows: deionized water is heated to 85 ℃ of temperature, the aluminium isopropoxide gradation that to dissolve with the cosolvent isopropyl alcohol while stirring behind the constant temperature slowly adds, wherein the molar ratio of aluminium isopropoxide and isopropyl alcohol is 1: 2, all add the back backflow and stirred 1.5 hours, form white precipitate; Be warming up to 95 ℃ again, after the stirring condition lower open mouth is evaporated to isopropyl alcohol and volatilizees fully, press aluminium isopropoxide: the amount of the mol ratio 1 of hydrochloric acid: 0.1-0.3 adds peptizing agent hydrochloric acid, and sediment is disperseed again, and ageing 4 hours obtains alumina sol; Adding accounts for the PVA of alumina sol total amount 0.2-0.4 weight % and the non-ionic surface active agent of 0.3-0.7 weight % in alumina sol then, evenly mixes and makes nano antistatic finishing agent.
Be preferably, the preparation method of nano antistatic finishing agent of the present invention, concrete steps are as follows:
Deionized water is heated to 85 ℃ of temperature, the aluminium isopropoxide gradation that to dissolve with the cosolvent isopropyl alcohol while stirring behind the constant temperature slowly adds, wherein the molar ratio of aluminium isopropoxide and isopropyl alcohol is 1: 2, all adds the back backflow and stirs 1.5 hours, forms white precipitate; Be warming up to 95 ℃ again, after the stirring condition lower open mouth is evaporated to isopropyl alcohol and volatilizees fully, press aluminium isopropoxide: the amount of the mol ratio 1 of hydrochloric acid: 0.1-0.3 adds peptizing agent hydrochloric acid, and sediment is disperseed again, and ageing 4 hours obtains alumina sol; In alumina sol, add then and account for the PVA of alumina sol total amount 0.3 weight % and the non-ionic surface active agent of 0.5 weight % makes nano antistatic finishing agent.
In the present invention, the finishing agent of preparation can be put in order fabric with padding method.
Fabrics such as terylene are immersed in the nano antistatic finishing agent of finite concentration such as 1-10 grams per liter, adopt the extruding of open width padding machine, two soak two rolls, control certain pick-up (70-100%), put into 100 ℃ of preliminary drying 5-10 of drying machine minutes, under 150-180 ℃ high temperature, bake 20-50 second then, promptly get qualified products.
This finishing agent of the present invention can be applicable in the fabrics antistatic arrangements such as terylene, polyamide fibre, acrylic fibers or polypropylene fibre.Described terylene is terylene clothes lining, terylene Curtains Fabrics and a polyester vehicle interior trim fabric etc.
To textiles antistatic finish effect, can adopt the half-life of testing friction static and the method for peak value electrostatic pressure to estimate.
The present invention can obtain splendid antistatic effect owing to adopt the nano grade inorganic material, and uses simply, and materials are economized, and cost is low and pollute few.
In the present invention, described PVA is a polyvinyl alcohol, and non-ionic surface active agent is general known reagent, for example can be 206 emulsifying agents, fatty alcohol-polyoxyethylene ether, alkylphenol polyoxyethylene, OP-10 or TX-10 etc.
The all raw material of Shi Yonging etc. all is conventional uses in the present invention, can buy from market.In the present invention, refer in particular to as non-, all amount, percentages are unit of weight.
Below in conjunction with embodiment the present invention is carried out concrete description.As known by the technical knowledge, the present invention can realize by other the embodiment that does not break away from its spiritual essence or essential feature.Therefore, following embodiment with regard to each side, all just illustrates, and is not only.All within the scope of the present invention or the change that is equal in the scope of the present invention all be included in the invention.
Four, the specific embodiment
Embodiment 1:
In the device that stirring, backflow and reinforced function are housed, deionized water is heated to 85 ℃, the constant temperature back is stirred the aluminium isopropoxide gradation that will dissolve with isopropyl alcohol on (mixing speed is 100rpm) limit and is slowly added, wherein the ratio of aluminium isopropoxide and isopropyl alcohol is 1: 2 (mol ratio), all add the back backflow and stirred 1.5 hours, form white precipitate.Be warming up to 95 ℃ again, after the stirring condition lower open mouth is evaporated to isopropyl alcohol and volatilizees fully, press aluminium isopropoxide: the mol ratio of hydrochloric acid 1: 0.1, add peptizing agent hydrochloric acid, sediment is disperseed again, ageing 4 hours, transparent (or translucent) alumina sol; Add the OP-10 in the PVA and 0.1% (weight) of alumina sol weight 0.1% (weight) in alumina sol, evenly stirring promptly makes nano antistatic finishing agent.
Embodiment 2:
In the reactor that stirring, backflow and reinforced function are housed, deionized water is heated to 80 ℃ of temperature, the constant temperature back is stirred the aluminium isopropoxide gradation that will dissolve with isopropyl alcohol on (mixing speed is 200rpm) limit and is slowly added, wherein the ratio of aluminium isopropoxide and isopropyl alcohol is 1: 3 (mol ratio), all add the back backflow and stirred 1 hour, form white precipitate.Be warming up to 90 ℃ again, the stirring condition lower open mouth be evaporated to produce isopropyl alcohol and volatilize fully after, press aluminium isopropoxide: the mol ratio of hydrochloric acid adds peptizing agent hydrochloric acid at 1: 0.3, and sediment is disperseed again, ageing 3 hours must transparent alumina colloidal sol.Add PVA and 1% (weight) TX-10 in alumina sol weight 0.5% (weight) in alumina sol, evenly stirring promptly makes nano antistatic finishing agent.
Embodiment 3:
In the reactor that stirring, backflow and reinforced function are housed, deionized water is heated to 75 ℃ of temperature, to add (adding total time is 30 minutes) with the aluminium isopropoxide gradation (three times) of cosolvent isopropyl alcohol dissolving is slow while stirring behind the constant temperature, wherein the ratio of aluminium isopropoxide and isopropyl alcohol is 1: 1 (mol ratio), all add the back backflow and stirred 2 hours, form white precipitate.Be warming up to 100 ℃ again, after the stirring condition lower open mouth is evaporated to isopropyl alcohol and volatilizees fully, press aluminium isopropoxide: the mol ratio of hydrochloric acid adds peptizing agent hydrochloric acid (watery hydrochloric acid) at 1: 0.2, stirs sediment is disperseed again, ageing 5 hours gets transparent (not exclusively) alumina sol.Add PVA and 0.5% (weight) TX-10 in alumina sol weight 0.3% (weight) in alumina sol, evenly stirring promptly makes nano antistatic finishing agent.
Embodiment 4
Polyester vehicle interior trim fabric is immersed in the nano antistatic finishing agent (as embodiment 1 preparation) of 10 grams per liters, adopt the extruding of open width padding machine, two soak two rolls, control pick-up 100%, put into 100 ℃ of preliminary drying 5-10 of drying machine minutes, and under 150-180 ℃ high temperature, baked 20-50 second then.Up to 3800V, after the finishing agent processing with 10 grams per liters, the electrostatic half-life of dacron dropped to 0.8 second to the electrostatic half-life of terylene inner decoration fabric greater than 90 seconds, electrostatic pressure before the arrangement, and electrostatic pressure drops to 27V.
Embodiment 5
Polyester vehicle interior trim fabric is immersed in the nano antistatic finishing agent (as embodiment 2 preparations) of 8 grams per liters, adopt the extruding of open width padding machine, two soak two rolls, control pick-up 90%, put into 100 ℃ of preliminary dryings of drying machine 8 minutes, and under 160 ℃ high temperature, baked 40 seconds then.Up to 4000V, after the finishing agent processing with 8 grams per liters, the electrostatic half-life of dacron dropped to 0.6 second to the electrostatic half-life of terylene inner decoration fabric greater than 100 seconds, electrostatic pressure before the arrangement, and electrostatic pressure drops to 20V.
Claims (10)
1, a kind of nano antistatic finishing agent is characterized in that containing alumina sol and in the PVA of alumina sol 0.1-0.5 weight % and the non-ionic surface active agent of 0.1-1 weight %.
2, nano antistatic finishing agent according to claim 1 is characterized in that containing in the PVA of alumina sol 0.2-0.4 weight % and the non-ionic surface active agent of 0.3-0.7 weight %.
3, nano antistatic finishing agent according to claim 1 is characterized in that containing in the PVA of alumina sol 0.3 weight % and the non-ionic surface active agent of 0.5 weight %.
4,, it is characterized in that described non-ionic surface active agent is an alkylphenol polyoxyethylene, OP-10 or TX-10 according to the described nano antistatic finishing agent of one of claim 1-3.
5, according to the described nano antistatic finishing agent of one of claim 1-4, it is characterized in that described alumina sol obtains by the following method: deionized water is heated to 75-85 ℃ of temperature, the aluminium isopropoxide gradation that to dissolve with isopropyl alcohol while stirring behind the constant temperature slowly adds, wherein the molar ratio of aluminium isopropoxide and isopropyl alcohol is 1: 1-3, all adding the back backflow stirred 1-2 hour, form white precipitate, be warming up to 90-100 ℃ again, after the stirring condition lower open mouth is evaporated to isopropyl alcohol and volatilizees fully, add peptizing agent hydrochloric acid, consumption is by aluminium isopropoxide: the mol ratio of hydrochloric acid is 1: 0.1-0.3, sediment is disperseed again, ageing 3-5 hour, get alumina sol.
6, according to the preparation method of one of claim 1-4 described nano antistatic finishing agent, it is characterized in that deionized water is heated to 75-85 ℃ of temperature, the aluminium isopropoxide gradation that to dissolve with the cosolvent isopropyl alcohol while stirring behind the constant temperature slowly adds, wherein the molar ratio of aluminium isopropoxide and isopropyl alcohol is 1: 1-3, all add the back backflow and stirred 1-2 hour, form white precipitate; Be warming up to 90-100 ℃ again, after the stirring condition lower open mouth is evaporated to isopropyl alcohol and volatilizees fully, press aluminium isopropoxide: the amount of the mol ratio 1 of hydrochloric acid: 0.1-0.3 adds peptizing agent hydrochloric acid, and sediment is disperseed again, ageing 3-5 hour, obtains alumina sol; In alumina sol, add the PVA of 0.1-0.5 weight % and the non-ionic surface active agent of 0.1-1 weight % then, evenly mix and make nano antistatic finishing agent.
7, the preparation method of nano antistatic finishing agent according to claim 6, it is characterized in that deionized water is heated to 85 ℃ of temperature, the aluminium isopropoxide gradation that to dissolve with the cosolvent isopropyl alcohol while stirring behind the constant temperature slowly adds, wherein the molar ratio of aluminium isopropoxide and isopropyl alcohol is 1: 2, all add the back backflow and stirred 1.5 hours, form white precipitate; Be warming up to 95 ℃ again, after the stirring condition lower open mouth is evaporated to isopropyl alcohol and volatilizees fully, press aluminium isopropoxide: the amount of the mol ratio 1 of hydrochloric acid: 0.1-0.3 adds peptizing agent hydrochloric acid, and sediment is disperseed again, and ageing 4 hours obtains alumina sol; In alumina sol, add the PVA of 0.2-0.4 weight % and the non-ionic surface active agent of 0.3-0.7 weight % then, evenly mix and make nano antistatic finishing agent.
8, the preparation method of nano antistatic finishing agent according to claim 6, it is characterized in that deionized water is heated to 85 ℃ of temperature, the aluminium isopropoxide gradation that to dissolve with isopropyl alcohol while stirring behind the constant temperature slowly adds, wherein the molar ratio of aluminium isopropoxide and isopropyl alcohol is 1: 2, all add the back backflow and stirred 1.5 hours, form white precipitate; Be warming up to 95 ℃ again, after the stirring condition lower open mouth is evaporated to isopropyl alcohol and volatilizees fully, press aluminium isopropoxide: the amount of the mol ratio 1 of hydrochloric acid: 0.1-0.3 adds peptizing agent hydrochloric acid, and sediment is disperseed again, and ageing 4 hours obtains alumina sol; In alumina sol, add the PVA of 0.3 weight % and the non-ionic surface active agent of 0.5 weight % then and make nano antistatic finishing agent.
9,, it is characterized in that this finishing agent is applied in terylene, polyamide fibre, acrylic fibers or the arrangement of polypropylene fibre fabrics antistatic according to the application of one of claim 1-4 described nano antistatic finishing agent.
10, the application of nano antistatic finishing agent according to claim 9 is characterized in that, described terylene is terylene clothes lining, terylene Curtains Fabrics and a polyester vehicle interior trim fabric.
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CN 200510117126 CN1760440A (en) | 2005-11-01 | 2005-11-01 | Nano antistatic finishing agent, preparation method and application |
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CN 200510117126 CN1760440A (en) | 2005-11-01 | 2005-11-01 | Nano antistatic finishing agent, preparation method and application |
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Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
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CN101136260B (en) * | 2007-08-29 | 2011-03-30 | 中国人民解放军总后勤部军需装备研究所 | Radioactive nucleus dust composite protection material and method for preparing the same |
CN103265774A (en) * | 2013-05-31 | 2013-08-28 | 苏州市景荣科技有限公司 | PVC (Polyvinyl Chloride) sole composite type antistatic agent and preparation method thereof |
CN105133291A (en) * | 2015-07-06 | 2015-12-09 | 苏州工业园区高性能陶瓷纤维工程中心有限公司 | Preparation method of alumina coating of silicon carbide fiber surface |
CN105369592A (en) * | 2015-10-20 | 2016-03-02 | 湖州国信物资有限公司 | Preparation method of alumina sol pure-cotton fabric antistatic finishing agent and arrangement method of alumina sol pure-cotton fabric |
CN107829305A (en) * | 2017-11-30 | 2018-03-23 | 安徽中福毛纺制帽有限公司 | A kind of special antistatic finishing agent of wool cap |
CN108532017A (en) * | 2018-04-09 | 2018-09-14 | 温州市赢创新材料技术有限公司 | A kind of antistatic hard fibre and preparation method thereof |
CN109385901A (en) * | 2018-10-26 | 2019-02-26 | 江苏华峰超纤材料有限公司 | Color antistatic superfine fibre flannelette material and preparation method thereof |
CN115075008A (en) * | 2022-07-01 | 2022-09-20 | 新乡市新科防护科技有限公司 | Efficient flame-retardant light, thin and soft multi-fiber blended fabric and preparation method thereof |
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2005
- 2005-11-01 CN CN 200510117126 patent/CN1760440A/en active Pending
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
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CN101136260B (en) * | 2007-08-29 | 2011-03-30 | 中国人民解放军总后勤部军需装备研究所 | Radioactive nucleus dust composite protection material and method for preparing the same |
CN103265774A (en) * | 2013-05-31 | 2013-08-28 | 苏州市景荣科技有限公司 | PVC (Polyvinyl Chloride) sole composite type antistatic agent and preparation method thereof |
CN103265774B (en) * | 2013-05-31 | 2015-08-05 | 苏州市景荣科技有限公司 | The preparation method of the compound antistatic agent of a kind of PVC sole |
CN105133291A (en) * | 2015-07-06 | 2015-12-09 | 苏州工业园区高性能陶瓷纤维工程中心有限公司 | Preparation method of alumina coating of silicon carbide fiber surface |
CN105369592A (en) * | 2015-10-20 | 2016-03-02 | 湖州国信物资有限公司 | Preparation method of alumina sol pure-cotton fabric antistatic finishing agent and arrangement method of alumina sol pure-cotton fabric |
CN107829305A (en) * | 2017-11-30 | 2018-03-23 | 安徽中福毛纺制帽有限公司 | A kind of special antistatic finishing agent of wool cap |
CN108532017A (en) * | 2018-04-09 | 2018-09-14 | 温州市赢创新材料技术有限公司 | A kind of antistatic hard fibre and preparation method thereof |
CN109385901A (en) * | 2018-10-26 | 2019-02-26 | 江苏华峰超纤材料有限公司 | Color antistatic superfine fibre flannelette material and preparation method thereof |
CN115075008A (en) * | 2022-07-01 | 2022-09-20 | 新乡市新科防护科技有限公司 | Efficient flame-retardant light, thin and soft multi-fiber blended fabric and preparation method thereof |
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