Nothing Special   »   [go: up one dir, main page]

CN106555245B - A kind of cut resistant ultra high molecular weight polyethylene fiber and its preparation method and application - Google Patents

A kind of cut resistant ultra high molecular weight polyethylene fiber and its preparation method and application Download PDF

Info

Publication number
CN106555245B
CN106555245B CN201510616997.8A CN201510616997A CN106555245B CN 106555245 B CN106555245 B CN 106555245B CN 201510616997 A CN201510616997 A CN 201510616997A CN 106555245 B CN106555245 B CN 106555245B
Authority
CN
China
Prior art keywords
molecular weight
high molecular
weight polyethylene
fiber
ultra high
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.)
Active
Application number
CN201510616997.8A
Other languages
Chinese (zh)
Other versions
CN106555245A (en
Inventor
贺鹏
黄兴良
杨媛媛
林凤崎
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Beijing Tong Yi Zhong new material Polytron Technologies Inc
Original Assignee
Beijing Tongyizhong Specialty Fiber Technology & Development Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Beijing Tongyizhong Specialty Fiber Technology & Development Co Ltd filed Critical Beijing Tongyizhong Specialty Fiber Technology & Development Co Ltd
Priority to CN201510616997.8A priority Critical patent/CN106555245B/en
Publication of CN106555245A publication Critical patent/CN106555245A/en
Application granted granted Critical
Publication of CN106555245B publication Critical patent/CN106555245B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Artificial Filaments (AREA)

Abstract

The present invention provides a kind of cut resistant ultra high molecular weight polyethylene fiber and its preparation method and application, the cut resistant ultra high molecular weight polyethylene fiber includes: ultra high molecular weight polyethylene fiber;The hard fibre and solvent naphtha being dispersed in the ultra high molecular weight polyethylene fiber;The mass ratio of the ultra high molecular weight polyethylene fiber, hard fibre and solvent naphtha is 100:(3~6): (0.3~2).Compared with prior art, cut resistant ultra high molecular weight polyethylene fiber provided by the invention is on the basis of meeting belt cutting-resisting property five grade standard of EN388, by solvent naphtha to the immersional wetting of hard fibre, keep hard fibre preferably compatible with ultra-high molecular weight polyethylene, simultaneously, the addition of solvent naphtha is conducive to hard fibre being uniformly distributed in ultra-high molecular weight polyethylene, makes finished fiber elongation at break with higher.

Description

A kind of cut resistant ultra high molecular weight polyethylene fiber and its preparation method and application
Technical field
The present invention relates to ultra high molecular weight polyethylene fiber technical fields, are that be related to a kind of cut resistant super more specifically High molecular weight polyethylene fiber and its preparation method and application.
Background technique
Ultra high molecular weight polyethylene fiber, also known as high-strength high-modulus polyethylene fiber, refer to by relative molecular weight 1,000,000 with On polyethylene spin come fiber.Since ultra high molecular weight polyethylene fiber has light weight, impact resistance, dielectric properties high The advantages that, it is widely used in aerospace field, sea area defence field, weaponry field and daily industrial circle.
In daily industrial circle, ultra high molecular weight polyethylene fiber is most commonly employed to the production that preparation has cut resistant function Product, for example, cut resistant gloves, cut resistant tent, cut resistant rope etc..But the supra polymer only prepared by polyethylene powders The belt cutting-resisting property of weight polyethylene fiber is limited, and it is anti-that the belt cutting-resisting property for the industrial gloves being made from it is only capable of reaching industrial gloves Protect the three-level requirement of European standard EN388 standard;And by adding glass fibre thereto, belt cutting-resisting property can be made to reach The Pyatyi requirement of EN388 standard, but flexibility due to glass fibre and comfort are poor, and practical application is unsatisfactory.Therefore, In practical application more be directed toward develop it is a kind of can reach EN388 Pyatyi requirement, simultaneously again soft comfortable supra polymer Weight polyethylene fiber is used to prepare the products such as industrial gloves.
Currently, people improve finished product by the way that ingredient, the spinning technique of improvement ultra high molecular weight polyethylene fiber etc. are many-sided The belt cutting-resisting property of fiber.Patent document US5976998 discloses a kind of filled cut-resistant fiber, the fiber by fibre-forming polymer and Hard filler of the Moh's scale number greater than 3 is made.But the granularity of the hard filler due to using is small, dosage is few, hard is filled out Material is difficult to reticulate distribution, therefore the ultra high molecular weight polyethylene fiber that this method obtains in ultra high molecular weight polyethylene fiber Cutting resistance be not improved.
Patent document WO2008046476 discloses a kind of cut resistant yarn, described it includes silk thread and/or staple fibre Silk thread and/or staple fibre include hard component for improving the cutting resistance of yarn, wherein the hard component is flat Equal diameter is up to 25 μm of more hard fibres.Although the cutting resistance for the ultra high molecular weight polyethylene fiber that this method obtains It is effectively improved, still, since hard component has lesser partial size and biggish specific surface area, hard component is inherently Easily reunite, and since spinning solution has viscosity, is difficult to be uniformly dispersed when hard component is mixed with spinning solution, lead Cause the elongation at break of finished fiber lower.
Summary of the invention
In view of this, the purpose of the present invention is to provide a kind of cut resistant ultra high molecular weight polyethylene fiber and its preparation sides The elongation at break of method and application, cut resistant ultra high molecular weight polyethylene fiber provided by the invention is high.
The present invention provides a kind of cut resistant ultra high molecular weight polyethylene fibers, comprising:
Ultra high molecular weight polyethylene fiber;
The hard fibre and solvent naphtha being dispersed in the ultra high molecular weight polyethylene fiber;
The mass ratio of the ultra high molecular weight polyethylene fiber, hard fibre and solvent naphtha is 100:(3~6): (0.3~ 2)。
Preferably, the weight average molecular weight of the ultra high molecular weight polyethylene fiber is 3.0 × 106~5 × 106, molecular weight point Cloth≤9.0.
Preferably, the hard fibre includes one of ceramic fibre, carbon fiber and silicon carbide whisker or a variety of.
Preferably, the average diameter of the hard fibre is greater than 0 and is less than or equal to 9 μm, and draw ratio is greater than 0 and is less than or equal to 30.
Preferably, the solvent naphtha is by 70%~95% cycloalkane containing 25~50 carbon atoms and 5%~30% Chain hydrocarbon composition containing 25~50 carbon atoms.
The present invention also provides a kind of preparations of cut resistant ultra high molecular weight polyethylene fiber described in above-mentioned technical proposal Method, comprising the following steps:
A) hard fibre and solvent naphtha are mixed, obtains mixed liquor A;
B) mixed liquor A is mixed with ultra-high molecular weight polyethylene lysate, obtains spinning solution;
C) spinning solution is successively spinned, preliminary draft, extraction, drying, screening and positive drawing-off, obtains cut resistant Ultra high molecular weight polyethylene fiber.
Preferably, the mass ratio of hard fibre described in step a), solvent naphtha and solvent naphtha is (3~6): (10~24).
Preferably, ultra-high molecular weight polyethylene lysate described in step b) includes:
100 parts by weight of ultra-high molecular weight polyethylene;
800 parts by weight of solvent naphtha~2800 parts by weight.
Preferably, the process of spinning described in step c) specifically:
The spinning solution is successively filtered, spinneret and cooling, obtains gel fiber.
The present invention also provides cut resistant ultra high molecular weight polyethylene fibers described in a kind of above-mentioned technical proposal as resistance to The application of cutting material.
It is described resistance to cut the present invention provides a kind of cut resistant ultra high molecular weight polyethylene fiber and its preparation method and application Cutting ultra high molecular weight polyethylene fiber includes: ultra high molecular weight polyethylene fiber;It is fine to be dispersed in the ultra-high molecular weight polyethylene Hard fibre and solvent naphtha in dimension;The mass ratio of the ultra high molecular weight polyethylene fiber, hard fibre and solvent naphtha is 100:(3~6): (0.3~2).Compared with prior art, cut resistant ultra high molecular weight polyethylene fiber provided by the invention is full On the basis of sufficient five grade standard of belt cutting-resisting property EN388, by solvent naphtha to the immersional wetting of hard fibre, make hard fibre with Ultra-high molecular weight polyethylene is preferably compatible, meanwhile, the addition of solvent naphtha is conducive to hard fibre in ultra-high molecular weight polyethylene In be uniformly distributed, make finished fiber elongation at break with higher.The experimental results showed that cut resistant provided by the invention is super The elongation at break of high molecular weight polyethylene fiber is 4%~5%.
Specific embodiment
Below in conjunction with the embodiment of the present invention, technical solution of the present invention is clearly and completely described, it is clear that institute The embodiment of description is only a part of the embodiment of the present invention, instead of all the embodiments.Based on the embodiments of the present invention, Every other embodiment obtained by those of ordinary skill in the art without making creative efforts, belongs to this hair The range of bright protection.
The present invention provides a kind of cut resistant ultra high molecular weight polyethylene fibers, comprising:
Ultra high molecular weight polyethylene fiber;
The hard fibre and solvent naphtha being dispersed in the ultra high molecular weight polyethylene fiber;
The mass ratio of the ultra high molecular weight polyethylene fiber, hard fibre and solvent naphtha is 100:(3~6): (0.3~ 2)。
In the present invention, the weight average molecular weight of the ultra high molecular weight polyethylene fiber is preferably 3.0 × 106~5 × 106, More preferably 3.5 × 106~4.5 × 106;The molecular weight distribution of the ultra high molecular weight polyethylene fiber is preferably≤9.0, more excellent It is selected as 5.0.In the present invention, the ultra high molecular weight polyethylene fiber is the cut resistant ultra high molecular weight polyethylene fiber Matrix, structural regularity with higher and consistency, so that making product integrally has the mechanical property of high-strength and high-modulus amount.
In the present invention, the hard fibre preferably include one of ceramic fibre, carbon fiber and silicon carbide whisker or It is a variety of, the more preferably mixture of ceramic fibre, carbon fiber and silicon carbide whisker.In the present invention, the hard fibre is institute The reinforcing material of cut resistant ultra high molecular weight polyethylene fiber is stated, the intensity of finished fiber can be effectively improved, it is resistance to improve product Cutting performance;The present invention is not particularly limited the source of the hard fibre, using well known to those skilled in the art above-mentioned The commercial goods of ceramic fibre, carbon fiber and silicon carbide whisker.In the present invention, the ceramic fibre, carbon fiber and carbon The mass ratio of ceramic fibre, carbon fiber and silicon carbide whisker is preferably 1:(7~8.8 in the mixture of SiClx whisker): (0.2~ 1), more preferably 1:(7.3~8.4): (0.25~0.8), most preferably 1:(7.5~8): (0.3~0.5).In the present invention, The average diameter of the hard fibre is preferably greater than 0 and is less than or equal to 9 μm, and more preferably greater than 0 is less than or equal to 7 μm;The hard is fine The draw ratio of dimension is preferably greater than 0 and is less than or equal to 30, more preferably greater than 0 less than or equal to 20.
In the present invention, the solvent naphtha preferably by 70%~95% the cycloalkane and 5% containing 25~50 carbon atoms ~30% chain hydrocarbon composition containing 25~50 carbon atoms, more preferably by 85%~90% the ring containing 25~50 carbon atoms Alkane and 10%~15% the chain hydrocarbon composition containing 25~50 carbon atoms, most preferably white oil.In the present invention, the solvent The kinematic viscosity of oil is preferably 61.2mm2/ s~74.8mm2/s;The present invention is not particularly limited the source of the solvent naphtha, adopts With 5# white oil well known to those skilled in the art, 7# white oil, 10# white oil, 15# white oil, 22# white oil, 26# white oil, 32# white oil, The commercial goods of 46# white oil, 68# white oil, 70# white oil, 100# white oil and 150# white oil.In the present invention, the solvent Oil plays the role of enhancing infiltration to hard fibre, bonds hard fibre preferably with ultra-high molecular weight polyethylene, together When, the addition of solvent naphtha is conducive to hard fibre being uniformly distributed in ultra-high molecular weight polyethylene, make finished fiber have compared with High elongation at break.
In the present invention, the mass ratio of the ultra high molecular weight polyethylene fiber, hard fibre and solvent naphtha is 100:(3 ~6): (0.3~2), preferably 100:(4~5): (0.8~1).
The present invention also provides a kind of preparations of cut resistant ultra high molecular weight polyethylene fiber described in above-mentioned technical proposal Method, comprising the following steps:
A) hard fibre and solvent naphtha are mixed, obtains mixed liquor A;
B) mixed liquor A is mixed with ultra-high molecular weight polyethylene lysate, obtains spinning solution;
C) spinning solution is successively spinned, preliminary draft, extraction, drying, positive drawing-off and screening, obtains cut resistant Ultra high molecular weight polyethylene fiber.
In the present invention, hard fibre and solvent naphtha are mixed, obtains mixed liquor A.In the present invention, the hard fibre Preferably include one of ceramic fibre, carbon fiber and silicon carbide whisker or a variety of, more preferably ceramic fibre, carbon fiber and carbon The mixture of SiClx whisker.In the present invention, the hard fibre is the increasing of the cut resistant ultra high molecular weight polyethylene fiber Strong material can be effectively improved the intensity of finished fiber, improve product belt cutting-resisting property;The present invention carrys out the hard fibre Source is not particularly limited, using the commercially available of above-mentioned ceramic fibre well known to those skilled in the art, carbon fiber and silicon carbide whisker Commodity.In the present invention, ceramic fibre, carbon fiber in the mixture of the ceramic fibre, carbon fiber and silicon carbide whisker Mass ratio with silicon carbide whisker is preferably 1:(7~8.8): (0.2~1), more preferably 1:(7.3~8.4): (0.25~ 0.8), most preferably 1:(7.5~8): (0.3~0.5).In the present invention, the average diameter of the hard fibre is preferably big It is less than or equal to 9 μm in 0, more preferably higher than 0 is less than or equal to 7 μm;The draw ratio of the hard fibre be preferably greater than 0 be less than etc. It is less than or equal to 20 in 30, more preferably higher than 0.
In the present invention, the solvent naphtha preferably by 70%~95% the cycloalkane and 5% containing 25~50 carbon atoms ~30% chain hydrocarbon composition containing 25~50 carbon atoms, more preferably by 85%~90% the ring containing 25~50 carbon atoms Alkane and 10%~15% the chain hydrocarbon composition containing 25~50 carbon atoms, most preferably white oil.In the present invention, the solvent The kinematic viscosity of oil is preferably 61.2mm2/ s~74.8mm2/s;The present invention is not particularly limited the source of the solvent naphtha, adopts With 5# white oil well known to those skilled in the art, 7# white oil, 10# white oil, 15# white oil, 22# white oil, 26# white oil, 32# white oil, The commercial goods of 46# white oil, 68# white oil, 70# white oil, 100# white oil and 150# white oil.In the present invention, the solvent Oil is the solvent of ultra-high molecular weight polyethylene lysate, and hard fibre and solvent naphtha are dispersed in solvent naphtha first by the present invention In, be conducive to the further dispersion of hard fibre and solvent naphtha in ultra high molecular weight polyethylene fiber.
In the present invention, after hard fibre and solvent naphtha being mixed, the kinematic viscosity of obtained mixed solution A can be according to hard The additional amount of matter fiber changes, and has an impact to the mechanical property of product, and additional amount is excessively high, the kinematic viscosity of mixed solution A It reduces, product broken end number can be made to increase, additional amount is too low, is unfavorable for the raising of fibre strength, makes the cutting resistance of product and strong Degree reduces.In the present invention, hard fibre, solvent naphtha and solvent naphtha are mixed;The mass ratio of the hard fibre and solvent naphtha Preferably (3~6): (10~24), more preferably (4~5): (14~20).
In the present invention, the mixed process is preferred specifically:
Hard fibre and solvent naphtha are mixed under stirring conditions.The present invention is to the method for the stirring without spy Different limitation, using artificial stirring well known to those skilled in the art or mechanical stirring.In the present invention, the speed of the stirring Degree is preferably 1000rpm~4500rpm, more preferably 2000rpm~3000rpm;The present invention is not special to the time of stirring Limitation, makes hard fibre be uniformly dispersed in solvent naphtha.
After obtaining the mixed liquor A, the present invention mixes the mixed liquor A with ultra-high molecular weight polyethylene lysate, obtains To spinning solution.In the present invention, the ultra-high molecular weight polyethylene lysate preferably includes:
100 parts by weight of ultra-high molecular weight polyethylene;
800 parts by weight of solvent naphtha~2800 parts by weight.
In the present invention, the ultra-high molecular weight polyethylene is molten in the solvent naphtha by ultra-high molecular weight polyethylene powder It is obtained after solution;The present invention is not particularly limited the source of the ultra-high molecular weight polyethylene powder, using those skilled in the art Commercial goods known to member.In the present invention, the weight average molecular weight of the ultra-high molecular weight polyethylene powder is preferably 3.0 ×106~5 × 106, more preferably 3.5 × 106~4.5 × 106;The molecular weight distribution of the ultra-high molecular weight polyethylene powder It is preferred that≤9.0, more preferably 5.0;The partial size of the ultra-high molecular weight polyethylene powder is preferably 40 mesh~100 mesh, more preferably For 60 mesh~80 mesh.In the present invention, the ultra-high molecular weight polyethylene lysate preferably includes ultra-high molecular weight polyethylene 100 Parts by weight.
In the present invention, the solvent naphtha preferably by 70%~95% the cycloalkane and 5% containing 25~50 carbon atoms ~30% chain hydrocarbon composition containing 25~50 carbon atoms, more preferably by 85%~90% the ring containing 25~50 carbon atoms Alkane and 10%~15% the chain hydrocarbon composition containing 25~50 carbon atoms, most preferably white oil.In the present invention, the solvent The initial boiling point of oil is higher than 450 DEG C;The kinematic viscosity of the solvent naphtha is preferably 61.2mm2/ s~74.8mm2/s;The present invention is to institute The source for stating solvent naphtha is not particularly limited, using 5# white oil well known to those skilled in the art, 7# white oil, 10# white oil, 15# White oil, 22# white oil, 26# white oil, 32# white oil, 46# white oil, 68# white oil, 70# white oil, 100# white oil and 150# white oil it is commercially available Commodity.In the present invention, the solvent naphtha in the ultra-high molecular weight polyethylene lysate with it is molten in the mixed solution A Agent oil is preferably identical solvent naphtha, is conducive to the miscible of the ultra-high molecular weight polyethylene lysate and the mixed solution A. In the present invention, the ultra-high molecular weight polyethylene lysate preferably includes 800 parts by weight of solvent naphtha~2800 parts by weight, more excellent It is selected as 1100 parts by weight~2000 parts by weight.
In the present invention, the preparation method of the ultra-high molecular weight polyethylene lysate is preferred specifically:
Ultra-high molecular weight polyethylene powder is mixed with solvent naphtha, obtains ultra-high molecular weight polyethylene lysate.In this hair In bright, the process that ultra-high molecular weight polyethylene powder is mixed with solvent naphtha is preferred specifically:
Ultra-high molecular weight polyethylene powder is added in solvent naphtha, is stirred, it is molten to obtain ultra-high molecular weight polyethylene Solve liquid.The present invention is not particularly limited the method for the stirring, using artificial stirring well known to those skilled in the art or machine Tool stirring.In the present invention, the speed of the stirring is preferably 30rpm~500rpm, and more preferably 60rpm~ 100rpm;The temperature of the stirring is preferably 80 DEG C~120 DEG C, more preferably 100 DEG C~110 DEG C;The time of the stirring is excellent It is selected as 0.5h~5h, more preferably 1h~2h.
In the present invention, the mixed liquor A is mixed with ultra-high molecular weight polyethylene lysate, obtains spinning solution.? In the present invention, the process that mixed liquor A is mixed with ultra-high molecular weight polyethylene lysate is preferred specifically:
Mixed liquor A is added in ultra-high molecular weight polyethylene lysate, is stirred, spinning solution is obtained.The present invention The method of the stirring is not particularly limited, using artificial stirring well known to those skilled in the art or mechanical stirring. In the present invention, the speed of the stirring is preferably 60rpm~100rpm, more preferably 80rpm~90rpm;The stirring Temperature is preferably 100 DEG C~160 DEG C, more preferably 120 DEG C~140 DEG C;The time of the stirring is preferably 1h~6h, more preferably For 2h~3h.
After obtaining spinning solution, the present invention successively spins the spinning solution, preliminary draft, extraction, drying, screening With positive drawing-off, cut resistant ultra high molecular weight polyethylene fiber is obtained.In the present invention, spinning solution is spinned, is frozen Collodion silk.In the present invention, the process of the spinning is preferred specifically:
The spinning solution is successively filtered, spinneret and cooling, obtains gel fiber.In the present invention, by the spinning Silk stock solution is filtered.The present invention is not particularly limited the equipment of the filtering, it is preferred to use filter;The filter Aperture is preferably 30 mesh~100 mesh, more preferably 60 mesh~70 mesh.
After completing the filter process, filtered spinning solution is carried out spinneret and cooling by the present invention, obtains gel fiber. In the present invention, the equipment of the spinneret is preferably manifold, and it is not specifically limited to this by the present invention;The present invention will be through manifold The product obtained after spinneret, is directly cooled down, and gel fiber is obtained.The present invention is not particularly limited the method for the cooling, It is preferred that using the technical solution of water-bath cooling well known to those skilled in the art;The temperature of the water-bath cooling is preferably 20 DEG C~ 30 DEG C, more preferably 22 DEG C~25 DEG C.
After completing the spinning process, the gel fiber obtained after spinning is carried out preliminary draft by the present invention.In the present invention, institute Stating preliminary draft can reduce the internal stress of gel fiber internal residual.In the present invention, the draft ratio of the preliminary draft is preferably 1 ~10 times, more preferably 3~5 times;The temperature of the preliminary draft is preferably 20 DEG C~30 DEG C, more preferably 25 DEG C.
After completing the preliminary draft process, the gel fiber after preliminary draft is extracted and is dried by the present invention.In the present invention In, the purpose of the extraction is the solvent naphtha removed in gel fiber.In the present invention, extractant used in the extraction process is excellent It is selected as one of white oil extractant, n-hexane, gasoline and tetrahydro carbon or a variety of.In the present invention, the extractant is to molten Agent oil has good intermiscibility, and the present invention is not particularly limited the source of the extractant, using those skilled in the art The commercial goods of well known above-mentioned white oil extractant, n-hexane, gasoline and tetrahydro carbon.In the present invention, the drying Purpose be that extractant is made to volatilize.In the present invention, the temperature of the drying is preferably 25 DEG C~45 DEG C, more preferably 30 DEG C~ 40℃。
After completing the extraction and drying process, the present invention screens the gel fiber after extraction and drying.In this hair In bright, the purpose of the screening is to control the content of the solvent naphtha in gel fiber;The present invention is to the method for the screening without spy Different limitation, using concentration detection method well known to those skilled in the art.In the present invention, the solvent naphtha is to hard fibre Dimension plays the role of enhancing infiltration, keeps hard fibre preferably compatible with ultra-high molecular weight polyethylene, meanwhile, the addition of solvent naphtha Be conducive to hard fibre being uniformly distributed in ultra-high molecular weight polyethylene, the pulling force in subsequent positive drafting process is enable to freeze It is continuous in collodion silk, uniformly transfer, improve draft ratio, finally make finished fiber elongation at break with higher, improve finished product The paracentesis resistance of fiber;But solvent oil content can excessively make hard fibre and ultra-high molecular weight polyethylene in positive drafting process Between biggish relative movement occurs, be broken finished fiber.In the present invention, the ultra-high molecular weight polyethylene is fine The mass ratio of dimension, hard fibre and solvent naphtha is 100:(3~6): (0.3~2), preferably 100:(3~6): (0.8~1).
After completing the screening process, the gel fiber after screening is carried out positive drawing-off by the present invention, obtains cut resistant superelevation point Sub- weight polyethylene fiber.In the present invention, the temperature of the positive drawing-off is preferably 120 DEG C~160 DEG C, more preferably 140 DEG C~ 150℃;The draft ratio of the positive drawing-off is preferably 7~30 times, and more preferably 15~20 times.In the present invention, described just to lead Stretching can make fiber deform, and obtain finished fiber, and the fibre deformation speed has a major impact the mechanical property of product, Deformation velocity such as fruit fiber is too fast, then fiber is broken before reaching enough draft ratios, and the deformation velocity of fiber It crosses slowly, then strand mitigates during stretching, cannot get high strength fibre.In the present invention, the deformation velocity of the fiber Preferably 0.005s-1~0.5s-1, more preferably 0.01s-1~0.1s-1
The present invention also provides cut resistant ultra high molecular weight polyethylene fibers described in a kind of above-mentioned technical proposal as resistance to The application of cutting material.In the present invention, the cut resistant material is the product with cut resistant function, preferably cut-resistant yarn Line.The present invention is not particularly limited the preparation method of the cut resistant yarn, using yarn well known to those skilled in the art The method of processing.In the present invention, the cut resistant yarn can be by being knitted or weaving to obtain different types of resistance to cut Cut product, such as cut resistant gloves, cut resistant tent, cut resistant rope.
It is described resistance to cut the present invention provides a kind of cut resistant ultra high molecular weight polyethylene fiber and its preparation method and application Cutting ultra high molecular weight polyethylene fiber includes: ultra high molecular weight polyethylene fiber;It is fine to be dispersed in the ultra-high molecular weight polyethylene Hard fibre and solvent naphtha in dimension;The mass ratio of the ultra high molecular weight polyethylene fiber, hard fibre and solvent naphtha is 100:(3~6): (1~3).Compared with prior art, cut resistant ultra high molecular weight polyethylene fiber provided by the invention is meeting On the basis of five grade standard of belt cutting-resisting property EN388, by solvent naphtha to the immersional wetting of hard fibre, keep hard fibre more preferable Bonded with ultra-high molecular weight polyethylene, meanwhile, the addition of solvent naphtha is conducive to hard fibre in superhigh molecular weight polyethylene Being uniformly distributed in alkene makes finished fiber elongation at break with higher.The experimental results showed that cut resistant provided by the invention The elongation at break of ultra high molecular weight polyethylene fiber is 4%~5%.
In addition, the uniformity of cut resistant ultra high molecular weight polyethylene fiber provided by the invention is preferable, quality stability is high, Industrial gloves belt cutting-resisting property obtained is excellent.
In order to further illustrate the present invention, it is described in detail below by following embodiment.Following embodiment of the present invention Ultra-high molecular weight polyethylene powder used is provided by Yanshan Petrochemical;Ceramic fibre used is mentioned by Shandong Luyang share co.,ltd For the average diameter of the ceramic fibre is less than or equal to 9 μm, and draw ratio is less than or equal to 30;Carbon fiber used multiple Condor carbon in Fiber Co., Ltd provides, and the average diameter of the carbon fiber is less than or equal to 9 μm, and draw ratio is less than or equal to 30;Silicon carbide used Whisker is provided by one promise new high-tech material development corporation, Ltd. of Qinhuangdao, and the average diameter of the silicon carbide whisker is less than or equal to 9 μm, Draw ratio is less than or equal to 30;White oil used is provided by Total SA;White oil extractant used strangles the limited public affairs of chemistry by Shanghai is uncommon Department provides.
Embodiment 1
(1) 50g ceramic fibre, 375g carbon fiber and 25g silicon carbide whisker are added in 1.8kg 68# white oil, It is stirred until homogeneous under 2500rpm, obtains mixed liquor A.
It (2) is 4.2 × 10 by 10kg weight average molecular weight6, molecular weight distribution be 5.0 ultra-high molecular weight polyethylene powder add Enter in 160kg 68# white oil, stirs 1.5h at 80rpm, 105 DEG C, obtain ultra-high molecular weight polyethylene lysate;Again described The mixed liquor A that step (1) obtains is added in ultra-high molecular weight polyethylene lysate, stirs 2.5h at 85rpm, 130 DEG C, obtains Spinning solution.
(3) filter that spinning solution via hole diameter is 60 mesh is filtered, then after manifold spinneret, product is lauched at 25 DEG C Bath cooling, obtains gel fiber;Then the gel fiber is subjected to preliminary draft with 4 times of draft ratio at 25 DEG C, then through white oil It is dry at 40 DEG C after extractant extraction, the gel fiber that 68# white oil quality is 0.09kg is obtained through screening, finally at 145 DEG C Positive drawing-off is carried out with 17 times of draft ratio, the deformation velocity for controlling fiber is 0.020s-1, it is poly- to obtain cut resistant super high molecular weight Vinyl fiber.
Embodiment 2
(1) 50g ceramic fibre, 385g carbon fiber and 15g silicon carbide whisker are added in 1.4kg 68# white oil, It is stirred until homogeneous under 2000rpm, obtains mixed liquor A.
It (2) is 3.5 × 10 by 10kg weight average molecular weight6, molecular weight distribution be 5.0 ultra-high molecular weight polyethylene powder add Enter in 110kg 68# white oil, stirs 2h at 60rpm, 100 DEG C, obtain ultra-high molecular weight polyethylene lysate;Again described super The mixed liquor A that step (1) obtains is added in High molecular weight polyethylene lysate, stirs 3h at 80rpm, 120 DEG C, obtains spinning Stoste.
(3) filter that spinning solution via hole diameter is 70 mesh is filtered, then after manifold spinneret, product is lauched at 22 DEG C Bath cooling, obtains gel fiber;Then the gel fiber is subjected to preliminary draft with 3 times of draft ratio at 25 DEG C, then through white oil It is dry at 40 DEG C after extractant extraction, the gel fiber that 68# white oil quality is 0.09kg is obtained through screening, finally at 140 DEG C Positive drawing-off is carried out with 18 times of draft ratio, the deformation velocity for controlling fiber is 0.025s-1, it is poly- to obtain cut resistant super high molecular weight Vinyl fiber.
Embodiment 3
(1) 56g ceramic fibre, 417g carbon fiber and 28g silicon carbide whisker are added in 2.0kg 68# white oil, It is stirred until homogeneous under 3000rpm, obtains mixed liquor A.
It (2) is 4.5 × 10 by 10kg weight average molecular weight6, molecular weight distribution be 5.0 ultra-high molecular weight polyethylene powder add Enter in 200kg 68# white oil, stirs 1h at 100rpm, 110 DEG C, obtain ultra-high molecular weight polyethylene lysate;Again described The mixed liquor A that step (1) obtains is added in ultra-high molecular weight polyethylene lysate, stirs 2h at 90rpm, 140 DEG C, is spun Silk stock solution.
(3) filter that spinning solution via hole diameter is 60 mesh is filtered, then after manifold spinneret, product is lauched at 25 DEG C Bath cooling, obtains gel fiber;Then the gel fiber is subjected to preliminary draft with 6 times of draft ratio at 25 DEG C, then through white oil It is dry at 40 DEG C after extractant extraction, the gel fiber that 68# white oil quality is 0.1kg is obtained through screening, finally at 150 DEG C Positive drawing-off is carried out with 15 times of draft ratio, the deformation velocity for controlling fiber is 0.0118s-1, obtain cut resistant super high molecular weight Polyethylene fibre.
Embodiment 4
(1) 450g ceramic fibre is added in 1.8kg 68# white oil, is stirred until homogeneous at 2500rpm, obtains mixed liquor A。
It (2) is 4.2 × 10 by 10kg weight average molecular weight6, molecular weight distribution be 5.0 ultra-high molecular weight polyethylene powder add Enter in 160kg 68# white oil, stirs 1.5h at 80rpm, 105 DEG C, obtain ultra-high molecular weight polyethylene lysate;Again described The mixed liquor A that step (1) obtains is added in ultra-high molecular weight polyethylene lysate, stirs 2.5h at 85rpm, 130 DEG C, obtains Spinning solution.
(3) filter that spinning solution via hole diameter is 60 mesh is filtered, then after manifold spinneret, product is lauched at 25 DEG C Bath cooling, obtains gel fiber;Then the gel fiber is subjected to preliminary draft with 4 times of draft ratio at 25 DEG C, then through white oil It is dry at 30 DEG C after extractant extraction, the gel fiber that 68# white oil quality is 0.08kg is obtained through screening, finally at 145 DEG C Positive drawing-off is carried out with 20 times of draft ratio, the deformation velocity for controlling fiber is 0.020s-1, it is poly- to obtain cut resistant super high molecular weight Vinyl fiber.
Embodiment 5
(1) 450g carbon fiber is added in 1.8kg 68# white oil, is stirred until homogeneous at 2500rpm, obtains mixed liquor A.
It (2) is 4.2 × 10 by 10kg weight average molecular weight6, molecular weight distribution be 5.0 ultra-high molecular weight polyethylene powder add Enter in 160kg 68# white oil, stirs 1.5h at 80rpm, 105 DEG C, obtain ultra-high molecular weight polyethylene lysate;Again described The mixed liquor A that step (1) obtains is added in ultra-high molecular weight polyethylene lysate, stirs 2.5h at 85rpm, 130 DEG C, obtains Spinning solution.
(3) filter that spinning solution via hole diameter is 60 mesh is filtered, then after manifold spinneret, product is lauched at 25 DEG C Bath cooling, obtains gel fiber;Then the gel fiber is subjected to preliminary draft with 4 times of draft ratio at 25 DEG C, then through white oil It is dry at 30 DEG C after extractant extraction, the gel fiber that 68# white oil quality is 0.03kg is obtained through screening, finally at 145 DEG C Positive drawing-off is carried out with 7 times of draft ratio, the deformation velocity for controlling fiber is 0.020s-1, it is poly- to obtain cut resistant super high molecular weight Vinyl fiber.
Embodiment 6
(1) 450g silicon carbide whisker is added in 1.8kg 68# white oil, is stirred until homogeneous, is mixed at 2500rpm Liquid A.
It (2) is 4.2 × 10 by 10kg weight average molecular weight6, molecular weight distribution be 5.0 ultra-high molecular weight polyethylene powder add Enter in 160kg 68# white oil, stirs 1.5h at 80rpm, 105 DEG C, obtain ultra-high molecular weight polyethylene lysate;Again described The mixed liquor A that step (1) obtains is added in ultra-high molecular weight polyethylene lysate, stirs 2.5h at 85rpm, 130 DEG C, obtains Spinning solution.
(3) filter that spinning solution via hole diameter is 60 mesh is filtered, then after manifold spinneret, product is lauched at 25 DEG C Bath cooling, obtains gel fiber;Then the gel fiber is subjected to preliminary draft with 4 times of draft ratio at 25 DEG C, then through white oil It is dry at 30 DEG C after extractant extraction, the gel fiber that 68# white oil quality is 0.2kg is obtained through screening, finally at 145 DEG C Positive drawing-off is carried out with 28 times of draft ratio, the deformation velocity for controlling fiber is 0.020s-1, it is poly- to obtain cut resistant super high molecular weight Vinyl fiber.
Examples 1 to 6 is mentioned using DXLL-20000 electronic tensile machine method according to specified in GBT 19975-2005 Fibre strength, modulus and the elongation at break of the cut resistant ultra high molecular weight polyethylene fiber of confession are tested, using YG086 type Measuring reel tests the fiber number for the cut resistant ultra high molecular weight polyethylene fiber that Examples 1 to 6 provides, and is connecing silk Broken end number is obtained in the process, and the broken end number is expressed as the every myriametre broken end number of finished fiber.Test result is as shown in table 1.
The fibre strength data for the cut resistant ultra high molecular weight polyethylene fiber that 1 Examples 1 to 6 of table provides
Embodiment 1 Embodiment 2 Embodiment 3 Embodiment 4 Embodiment 5 Embodiment 6
Intensity (cN/dtex) 25.8 25.5 26.5 25.5 25.2 26.8
Modulus (cN/dtex) 900 912 970 875 871 961
Fiber number (denier) 512.5 490.5 629 612.5 335.5 645.5
Elongation at break (%) 5.0 4.8 4.9 4.1 4.9 4.0
Break end number (a/myriametre) 0.5 0.6 1.3 0.8 1.5 1.1
Using the intensity for the cut resistant ultra high molecular weight polyethylene fiber that Instron type puller system provides Examples 1 to 6 Change rate is tested, while being provided using YG086 type measuring reel Examples 1 to 6
Cut resistant ultra high molecular weight polyethylene fiber distinguish a large amount of fiber number data of follow-on test, then pass through variance meter Fiber number coefficient of variation CV value is calculated, test result is as shown in table 2.
The change rate of strength data for the cut resistant ultra high molecular weight polyethylene fiber that 2 Examples 1 to 6 of table provides
Embodiment 1 Embodiment 2 Embodiment 3 Embodiment 4 Embodiment 5 Embodiment 6
Change rate of strength 3.1% 3.3% 4.0% 4.5% 4.8% 5.0%
Fiber number coefficient of variation CV 1.0% 0.9% 1.4% 1.2% 1.3% 1.5%
It is higher that test result shows that the cut resistant ultra high molecular weight polyethylene fiber that the embodiment of the present invention 1~6 provides has Fibre strength, while the change rate of strength of finished fiber is lower, i.e., strength stability is good;In addition, the product fiber number coefficient of variation CV is lower, while product elongation at break is stablized, and broken end number is lower, to guarantee that product has preferable uniformity and quality steady It is qualitative.
The cut resistant ultra high molecular weight polyethylene fiber that Example 1~6 provides, is twined along spool by positive and negative direction respectively Around, the cut resistant yarn of 400D is made, then above-mentioned cut resistant yarn is coated, is woven, respectively obtain cut resistant industry Gloves.European standard EN388 standard is protected according to industrial gloves, opponent, which covers, carries out anti-cut performance test, and number is worn out in measurement, Two samples are taken every time, are measured five times, and average value is calculated according to coefficient.Test result is as shown in table 3.
The cut resistant ultra high molecular weight polyethylene fiber belt cutting-resisting property data that 3 Examples 1 to 6 of table provides
Anti-cut (secondary) Five grade standard of EN388
Embodiment 1 25 Anti-cut >=20 time
Embodiment 2 23 Anti-cut >=20 time
Embodiment 3 28 Anti-cut >=20 time
Embodiment 4 23 Anti-cut >=20 time
Embodiment 5 21 Anti-cut >=20 time
Embodiment 6 25 Anti-cut >=20 time
As shown in Table 3, the belt cutting-resisting property of cut resistant ultra high molecular weight polyethylene fiber provided by the invention is preferable, is made Gloves can reach five grade standard of EN388.
The above description of the disclosed embodiments, enables those skilled in the art to implement or use the present invention.It is right A variety of modifications of these embodiments will be readily apparent to those skilled in the art, and as defined herein one As principle can realize in other embodiments without departing from the spirit or scope of the present invention.Therefore, the present invention will It will not be intended to be limited to the embodiments shown herein, and be to fit to consistent with the principles and novel features disclosed herein Widest scope.

Claims (8)

1. a kind of cut resistant ultra high molecular weight polyethylene fiber characterized by comprising
Ultra high molecular weight polyethylene fiber;The weight average molecular weight of the ultra high molecular weight polyethylene fiber is 3.0 × 106~5 × 106, molecular weight distribution≤9.0;
The hard fibre and solvent naphtha being dispersed in the ultra high molecular weight polyethylene fiber;
The mass ratio of the ultra high molecular weight polyethylene fiber, hard fibre and solvent naphtha is 100:(4~5): (0.3~2);
The preparation method of the cut resistant ultra high molecular weight polyethylene fiber, comprising the following steps:
A) hard fibre and solvent naphtha are mixed, obtains mixed liquor A;
B) mixed liquor A is mixed with ultra-high molecular weight polyethylene lysate, obtains spinning solution;
C) spinning solution is successively spinned, preliminary draft, extraction, drying, screening and positive drawing-off, obtains cut resistant superelevation Molecular weight polyethylene fiber;
The temperature of the positive drawing-off is 140 DEG C~150 DEG C, and draft ratio is 7~30 times, and the deformation velocity for controlling fiber is 0.01s-1~0.1s-1
2. cut resistant ultra high molecular weight polyethylene fiber according to claim 1, which is characterized in that the hard fibre packet Include one of ceramic fibre, carbon fiber and silicon carbide whisker or a variety of.
3. cut resistant ultra high molecular weight polyethylene fiber according to claim 1, which is characterized in that the hard fibre Average diameter is greater than 0 and is less than or equal to 9 μm, and draw ratio is greater than 0 and is less than or equal to 30.
4. cut resistant ultra high molecular weight polyethylene fiber according to claim 1, which is characterized in that the solvent naphtha by 70%~95% cycloalkane for containing 25~50 carbon atoms and 5%~30% chain hydrocarbon containing 25~50 carbon atoms form.
5. cut resistant ultra high molecular weight polyethylene fiber according to claim 1, which is characterized in that hard described in step a) The mass ratio of matter fiber and solvent naphtha is (3~6): (10~24).
6. cut resistant ultra high molecular weight polyethylene fiber according to claim 1, which is characterized in that surpass described in step b) High molecular weight polyethylene lysate includes:
100 parts by weight of ultra-high molecular weight polyethylene;
800 parts by weight of solvent naphtha~2800 parts by weight.
7. cut resistant ultra high molecular weight polyethylene fiber according to claim 1, which is characterized in that spun described in step c) The process of system specifically:
The spinning solution is successively filtered, spinneret and cooling, obtains gel fiber.
8. a kind of described in any item cut resistant ultra high molecular weight polyethylene fibers of claim 1~7 are as cut resistant material Using.
CN201510616997.8A 2015-09-24 2015-09-24 A kind of cut resistant ultra high molecular weight polyethylene fiber and its preparation method and application Active CN106555245B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510616997.8A CN106555245B (en) 2015-09-24 2015-09-24 A kind of cut resistant ultra high molecular weight polyethylene fiber and its preparation method and application

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510616997.8A CN106555245B (en) 2015-09-24 2015-09-24 A kind of cut resistant ultra high molecular weight polyethylene fiber and its preparation method and application

Publications (2)

Publication Number Publication Date
CN106555245A CN106555245A (en) 2017-04-05
CN106555245B true CN106555245B (en) 2019-04-30

Family

ID=58414138

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510616997.8A Active CN106555245B (en) 2015-09-24 2015-09-24 A kind of cut resistant ultra high molecular weight polyethylene fiber and its preparation method and application

Country Status (1)

Country Link
CN (1) CN106555245B (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107326462B (en) * 2017-06-20 2018-05-11 浙江金昊特种纤维有限公司 A kind of preparation method of wear-resisting anti-cutting superhigh molecular weight polyethylene fibers
CN107313124A (en) * 2017-06-23 2017-11-03 安徽长青藤新材料有限公司 Ultrashort fine enhancing ultra-high molecular weight polyethylene composite fibre and its manufacture method
CN109629028A (en) * 2018-11-15 2019-04-16 南通强生安全防护科技股份有限公司 A kind of graphene ultra-high molecular weight polyethylene composite fibre and preparation method thereof
CN110241472B (en) 2019-07-18 2020-05-19 星宇安防科技股份有限公司 Ultrahigh-molecular-weight polyethylene fiber with ultrahigh cutting resistance and preparation method thereof
CN113638106A (en) * 2021-09-03 2021-11-12 青岛信泰科技有限公司 Crease-resistant polyethylene fiber cloth and preparation method thereof
CN113829710A (en) * 2021-09-23 2021-12-24 青岛信泰科技有限公司 Polyethylene fiber cloth capable of effectively enhancing scratch resistance and preparation method thereof
CN113696564A (en) * 2021-09-23 2021-11-26 青岛信泰科技有限公司 Polyethylene fiber cloth capable of absorbing sweat on skin surface and preparation method thereof
CN115787121A (en) * 2022-12-12 2023-03-14 浙江千禧龙纤特种纤维股份有限公司 Cutting-resistant ultra-high molecular weight polyethylene fiber and preparation method and application thereof
CN116427047A (en) * 2023-04-14 2023-07-14 汇鸿(南通)安全用品有限公司 Preparation method of polyolefin fiber, and product and application thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101307509A (en) * 2007-05-15 2008-11-19 胡盼盼 Ultra-high molecular weight polyethylene fiber spinning method
CN101886295A (en) * 2009-05-11 2010-11-17 胡盼盼 Ultra-high molecular weight polyethylene colored fibers and preparation method thereof
CN102277669A (en) * 2006-10-17 2011-12-14 帝斯曼知识产权资产管理有限公司 Cut resistant yarn, a process for producing the yarn and products containing the yarn
CN102534838A (en) * 2010-12-07 2012-07-04 北京同益中特种纤维技术开发有限公司 Ultra-high molecular weight polyethylene fiber spinning stock solution and preparation method thereof
CN104746165A (en) * 2015-04-07 2015-07-01 中国科学技术大学 Ultra-high molecular weight polyethylene porous fiber and preparation method thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102277669A (en) * 2006-10-17 2011-12-14 帝斯曼知识产权资产管理有限公司 Cut resistant yarn, a process for producing the yarn and products containing the yarn
CN101307509A (en) * 2007-05-15 2008-11-19 胡盼盼 Ultra-high molecular weight polyethylene fiber spinning method
CN101886295A (en) * 2009-05-11 2010-11-17 胡盼盼 Ultra-high molecular weight polyethylene colored fibers and preparation method thereof
CN102534838A (en) * 2010-12-07 2012-07-04 北京同益中特种纤维技术开发有限公司 Ultra-high molecular weight polyethylene fiber spinning stock solution and preparation method thereof
CN104746165A (en) * 2015-04-07 2015-07-01 中国科学技术大学 Ultra-high molecular weight polyethylene porous fiber and preparation method thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
"UHMWPE 冻胶纤维除油率的研究及其对成品性能的影响";许海霞等;《合成纤维》;20101231(第2期);第21-25,30页

Also Published As

Publication number Publication date
CN106555245A (en) 2017-04-05

Similar Documents

Publication Publication Date Title
CN106555245B (en) A kind of cut resistant ultra high molecular weight polyethylene fiber and its preparation method and application
CN106555244B (en) A kind of cut resistant ultra high molecular weight polyethylene fiber and its preparation method and application
CN106555243B (en) A kind of cut resistant ultra high molecular weight polyethylene fiber and its preparation method and application
CN106555246B (en) A kind of cut resistant ultra high molecular weight polyethylene fiber and its preparation method and application
CN105734708B (en) A kind of preparation method of cut resistant superhigh molecular weight polyethylene fibers
CN109610029B (en) Fibers, fabrics and methods of making the same
CN109629028A (en) A kind of graphene ultra-high molecular weight polyethylene composite fibre and preparation method thereof
CN106350882A (en) Cutting-resistant ultra high molecular weight polyethylene fiber, preparation method and application thereof
CN106555247B (en) A kind of cut resistant ultra high molecular weight polyethylene fiber and its preparation method and application
TWI671444B (en) High performance multifilament
CN107419354A (en) High cut resistant high-strength high-modulus polyethylene long filament and preparation method thereof
CN108277546A (en) A kind of preparation method of anti-cutting polyethylene fibre
CN113897696A (en) Preparation method of anti-cutting polyamide 6 fiber
CN110273209A (en) A kind of high-strength fire-retarding high temperature resistant type polyimides yarn and preparation method thereof
CN108486676A (en) A kind of modifying nanometer cellulose acrylic fiber, preparation method and use
JP7268683B2 (en) Polyethylene fiber and products using it
JP7070667B2 (en) Polyethylene fiber and products using it
JP6874468B2 (en) Polyethylene fiber and products using it
WO2022014391A1 (en) Polyethylene fiber and product containing said fiber
CN109183426A (en) A kind of amorphous alloy stab-resistance body armor and preparation method thereof
CN107541802A (en) Short fibre of soft, wear-resistant and its production and use
JP2003027333A (en) Polyketone fiber
WO2021039528A1 (en) Acrylic fiber, and spun yarn and knitted fabric comprising said fiber
JPH06341016A (en) Black mass-colored polyamide fiber having high toughness
JP4332775B2 (en) Minimal metal composite fiber and method for producing the same

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant
CP03 Change of name, title or address
CP03 Change of name, title or address

Address after: 100176 901 Workshop, No. 16 Zhonghe Street, Beijing Economic and Technological Development Zone

Patentee after: Beijing Tong Yi Zhong new material Polytron Technologies Inc

Address before: 101102 No. 17, Jingshengnan Second Street, Majuqiao, Tongzhou District, Beijing

Patentee before: Beijing Tongyizhong Specialty Fiber Technology & Development Co., Ltd.