CN102851766A - Anti-ultraviolet fiber production method - Google Patents

Anti-ultraviolet fiber production method Download PDF

Info

Publication number
CN102851766A
CN102851766A CN2012103110822A CN201210311082A CN102851766A CN 102851766 A CN102851766 A CN 102851766A CN 2012103110822 A CN2012103110822 A CN 2012103110822A CN 201210311082 A CN201210311082 A CN 201210311082A CN 102851766 A CN102851766 A CN 102851766A
Authority
CN
China
Prior art keywords
ultraviolet
parts
finishing agent
antiultraviolet
master batch
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
Application number
CN2012103110822A
Other languages
Chinese (zh)
Inventor
蒋建业
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.)
KUNSHAN TIENIU SHIRT FACTORY
Original Assignee
KUNSHAN TIENIU SHIRT FACTORY
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 KUNSHAN TIENIU SHIRT FACTORY filed Critical KUNSHAN TIENIU SHIRT FACTORY
Priority to CN2012103110822A priority Critical patent/CN102851766A/en
Publication of CN102851766A publication Critical patent/CN102851766A/en
Pending legal-status Critical Current

Links

Landscapes

  • Artificial Filaments (AREA)

Abstract

The invention discloses an anti-ultraviolet fiber production method. The method comprises the following steps: 1, anti-ultraviolet master batch preparation: blending an anti-ultraviolet finishing agent with a carrier resin, drying, carrying out melt blending extrusion in a spiral extruder, and granulating to obtain anti-ultraviolet master batches; and 2, anti-ultraviolet fiber production: blending the anti-ultraviolet master batches with fiber slices, spinning, reeling, and stretching to obtain anti-ultraviolet fibers, wherein the anti-ultraviolet finishing agent comprises 25-35 parts by weight of zinc oxide, 5-8 parts by weight of zeolite, 20-23 parts by weight of 2-(2'-hydroxy-5'-methylphenyl)benzotriazole, 15-25 parts by weight of bis(3,5-di-tert-butyl-4-hydroxy)benzylphosphonatemonoethylate and 0.5-0.7 parts by weight of a sodium polyacrylate dispersant. The anti-ultraviolet finishing agent used in the invention simultaneously has the advantages of two anti-ultraviolet finishing agents, can be firmly combined with fibers and has a strong durability, and the anti-ultraviolet fibers have the advantages of excellent anti-ultraviolet effect, non-toxicity, and safety.

Description

The production method of ultraviolet prevention fiber
Technical field
The present invention relates to a kind of production method of ultraviolet prevention fiber.
Background technology
In general, suitable ultraviolet ray is useful to human body, and it can promote the synthetic of vitamin D, rickets is had inhibitory action, and have sterilization.But in recent years; because the chlorofluorination hydrocarbon compound in fluorine Lyons and so on is discharged in human being's production and life in large quantities; the umbrella that makes the earth is that atmosphere is destroyed day by day; at terrestrial pole and the sky, China Qinghai-Tibet Platean the ozone cavity has appearred particularly; the guard circle of the earth is that the ozone layer attenuation is thinning; the amount of ultraviolet irradiation that arrives ground increases, and the disease that causes because of excessive ultraviolet ray irradiation gets more and more.Generally speaking, human body skin can be accepted ultraviolet safe amount of radiation every day should be in 20kJ/m2, and the amount of radiation that ultraviolet ray arrives ground about 40~60kJ/m2 during the cloudy day, about 80~100kJ/m2 when fine, can reach 100~200kJ/m2 during scorching sun in hot summer days, common dress material generally about 50%, does not reach requirement of shelter to ultraviolet screening rate far away.In addition, long-term ultraviolet ray irradiation also can cause fading of textiles and aging.Therefore, be necessary textiles is carried out anti-ultraviolet finishing.
When illumination was mapped on the object, a part was reflected by body surface; Part is absorbed by object; Other then see through object.Fiber and goods with ultraviolet protection function, when UV-irradiation, except wherein the hole of a part from fabric sees through (its transit dose tissue of looking fabric with thickness etc. different), not not reflected by ultra-violet protecting agent of other, selectively absorbed exactly, and become heat energy to discharge its power conversion, to reach the ultraviolet purpose of minimizing.Strictly say, can be with the material of ultraviolet reflection ultraviolet light screener, to ultraviolet ray have strong selective absorb and can carry out power conversion and the material of transit dose that reduces it ultra-violet absorber.But in fact shielding exists simultaneously with absorption, and they have improved the ultraviolet protection function of fiber and textiles from different approach.
Kinds of fibers is different, and its ultraviolet ray transmissivity is also different.The natural fabrics such as cotton, real silk are low to ultraviolet absorbability, thereby antiultraviolet line poor performance, and wherein COTTON FABRIC is the most meable fabric of ultraviolet ray.
Uvioresistant finishing agent commonly used divides inorganic and organic two large classes at present.Uvioresistant finishing agent commonly used is metal, metal oxide and its esters, for example TiO mostly 2, ZnO, Al 2O 3, kaolin, talcum powder, carbon black, iron oxide, lead monoxide and CaCO 3Deng.Inorganic uvioresistant finishing agent and fabric fibre binding ability are relatively poor.Organic uvioresistant finishing agent mainly is to absorb ultraviolet ray and carry out power conversion, ultraviolet ray is become low-energy heat energy or the shorter electromagnetic wave of wavelength, thereby reach the purpose of ultraviolet radiation preventing.Generally have conjugated structure or hydrogen bond.Such uvioresistant finishing agent has certain toxicity.
Develop a kind of ultraviolet prevention fiber that is non-toxic and safe, has an excellent durability again and become important research topic.
Summary of the invention
The technical problem to be solved in the present invention provides a kind of production method of ultraviolet prevention fiber, the defects that exists to overcome prior art.
For solving the problems of the technologies described above, the production method of ultraviolet prevention fiber of the present invention comprises the steps:
1) antiultraviolet master batch preparation: with anti-ultraviolet finishing agent and vector resin blending, drying, enter the extruser melt blending and extrude, granulation obtains the antiultraviolet master batch;
2) ultraviolet prevention fiber production: after antiultraviolet master batch and fibre section blend, after spinning, coiling, stretching, form ultraviolet prevention fiber.
Described anti-ultraviolet finishing agent is comprised of the component of following weight portion:
25~35 parts in zinc oxide;
5~8 parts in zeolite;
2-(2 '-hydroxyl-5 '-aminomethyl phenyl) 20~23 parts of benzotriazole;
15~25 parts of two (3,5-di-t-butyl-4-hydroxyl) benzylphosphonic acid mono ethyl esters;
0.5~0.7 part of Sodium Polyacrylate dispersant.
Anti-ultraviolet finishing agent content is 5~20wt% in the antiultraviolet master batch.
Antiultraviolet master batch and fibre section 1: 10 in mass ratio~20 mixes.
The ultraviolet prevention fiber production technology is identical with similar conventional fibre production technology.For example, the production of antiultraviolet terylene, gram adds a certain proportion of antiultraviolet polyester master particle in the polyester slice, fully mixes in rotary drum dryer, drying, to reach homodisperse purpose.Process conditions and process are pressed the drying process of polyester slice and are implemented.During spinning, spinning machine winding speed 3200m/min, draw false twist texturing machine draft speed 150~800m/min; 282~288 ℃ of spinning temperatures.
Anti-ultraviolet finishing agent can adopt general mixed method, preferably adopts following method preparation:
With 2-(2 '-hydroxyl-5 '-aminomethyl phenyl) benzotriazole, two (3,5-di-t-butyl-4-hydroxyl) benzylphosphonic acid mono ethyl ester and zeolite mix, then slowly add simultaneously zinc oxide and Sodium Polyacrylate dispersant, feed intake in 1~2 hour complete, continue to mix 20~30 minutes.
As a kind of preferred version, preferred average grain diameter 300~1500 nanometers of described zinc oxide;
Described Sodium Polyacrylate dispersant preferred viscosities 300~350mPas.
The present invention organically combines inorganic and organic anti-ultraviolet finishing agent, and selected specific auxiliary agent is composited, and has the advantage of two kinds of anti-ultraviolet finishing agents concurrently, can with the fibr tissue strong bonded, durability is strong, and fabric is had good anti-ultraviolet effect, non-toxic and safe.
The specific embodiment
Embodiment 1
The preparation of anti-ultraviolet finishing agent:
With 2-(2 '-hydroxyl-5 '-aminomethyl phenyl) benzotriazole 20 gram, two (3,5-di-t-butyl-4-hydroxyl) benzylphosphonic acid mono ethyl ester 18 grams and zeolite 6 grams mix, then slowly add simultaneously zinc oxide 28 grams and Sodium Polyacrylate dispersant 0.5 gram, feed intake in 1 hour complete, continue to mix 20 minutes.
The preparation of antiultraviolet master batch:
With anti-ultraviolet finishing agent and vector resin blending, drying, enter the extruser melt blending and extrude, granulation obtains the antiultraviolet master batch, and anti-ultraviolet finishing agent accounts for 10wt% in the antiultraviolet master batch;
Ultraviolet prevention fiber is produced:
After antiultraviolet master batch and fibre section blend, after spinning, coiling, stretching, form ultraviolet prevention fiber.
Embodiment 2
The preparation of anti-ultraviolet finishing agent:
With 2-(2 '-hydroxyl-5 '-aminomethyl phenyl) benzotriazole 22 gram, two (3,5-di-t-butyl-4-hydroxyl) benzylphosphonic acid mono ethyl ester 25 grams and zeolite 5 grams mix, then slowly add simultaneously zinc oxide 32 grams and Sodium Polyacrylate dispersant 0.7 gram, feed intake in 1 hour complete, continue to mix 30 minutes.
The preparation of antiultraviolet master batch:
With anti-ultraviolet finishing agent and vector resin blending, drying, enter the extruser melt blending and extrude, granulation obtains the antiultraviolet master batch, and anti-ultraviolet finishing agent accounts for 10wt% in the antiultraviolet master batch;
Ultraviolet prevention fiber is produced:
After antiultraviolet master batch and fibre section blend, after spinning, coiling, stretching, form ultraviolet prevention fiber.
Application Example
1, durability
With containing the neutral detergent of 1 grams per liter with the ratio of 1: 50 fiber and detergent solution, washing is 30 minutes about 60 ℃ with fiber, and is dry about 60 ℃ behind the centrifuge dewatering.Wash respectively as stated above 5 times, 30 times.
2, ultraviolet resistance
Method according to standard GB/T-T 18830-2002 " evaluation of ultraviolet resistance of fabric " is measured the ultraviolet resistance of fiber under different wash conditions, and the result is as follows:
Ultraviolet resistance behind the different washing times of table 1
A represents that b represents to wash 5 times without the fiber of washing in the table, and c represents to wash 30 times.
As seen, the preventing ultraviolet effect of ultraviolet prevention fiber of the present invention is excellent, and has good wash durability, through repeatedly still having good ultraviolet resistance after the washing.

Claims (6)

1. the production method of ultraviolet prevention fiber is characterized in that, comprises the steps: 1) antiultraviolet master batch preparation: with anti-ultraviolet finishing agent and vector resin blending, drying, enter the extruser melt blending and extrude, granulation obtains the antiultraviolet master batch; 2) ultraviolet prevention fiber production: after antiultraviolet master batch and fibre section blend, after spinning, coiling, stretching, form ultraviolet prevention fiber;
Described anti-ultraviolet finishing agent is comprised of the component of following weight portion:
25~35 parts in zinc oxide;
5~8 parts in zeolite;
2-(2 '-hydroxyl-5 '-aminomethyl phenyl) 20~23 parts of benzotriazole;
15~25 parts of two (3,5-di-t-butyl-4-hydroxyl) benzylphosphonic acid mono ethyl esters;
0.5~0.7 part of Sodium Polyacrylate dispersant.
2. method according to claim 1, it is characterized in that, anti-ultraviolet finishing agent adopts the preparation of following method: with 2-(2 '-hydroxyl-5 '-aminomethyl phenyl) benzotriazole, two (3,5-di-t-butyl-4-hydroxyl) benzylphosphonic acid mono ethyl ester and zeolite mix, then slowly add simultaneously zinc oxide and Sodium Polyacrylate dispersant, feed intake in 1~2 hour complete, continue to mix 20~30 minutes.
3. method according to claim 1 is characterized in that, anti-ultraviolet finishing agent content is 5~20wt% in the antiultraviolet master batch.
4. method according to claim 1 is characterized in that, antiultraviolet master batch and fibre section 1: 10 in mass ratio~20 mixes.
5. method according to claim 1 is characterized in that, described zinc oxide average grain diameter 300~1500 nanometers.
6. method according to claim 1 is characterized in that, described Sodium Polyacrylate dispersant viscosity 300~350mPas.
CN2012103110822A 2012-08-29 2012-08-29 Anti-ultraviolet fiber production method Pending CN102851766A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2012103110822A CN102851766A (en) 2012-08-29 2012-08-29 Anti-ultraviolet fiber production method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2012103110822A CN102851766A (en) 2012-08-29 2012-08-29 Anti-ultraviolet fiber production method

Publications (1)

Publication Number Publication Date
CN102851766A true CN102851766A (en) 2013-01-02

Family

ID=47398725

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2012103110822A Pending CN102851766A (en) 2012-08-29 2012-08-29 Anti-ultraviolet fiber production method

Country Status (1)

Country Link
CN (1) CN102851766A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103469559A (en) * 2013-08-21 2013-12-25 昆山铁牛衬衫厂 UV-resistant composite finishing agent and preparation method thereof
CN107059159A (en) * 2017-05-19 2017-08-18 江苏华昌织物有限公司 A kind of preparation method of anti-aging shading screen cloth
CN107200981A (en) * 2017-07-19 2017-09-26 成都新柯力化工科技有限公司 A kind of antiultraviolet plastic matrix and preparation method
CN107604458A (en) * 2017-10-31 2018-01-19 上海稀美师塑料着色科技有限公司 A kind of preparation method of durable uvioresistant polypropylene fibre
CN108456947A (en) * 2018-01-12 2018-08-28 浙江东太新材料有限公司 A kind of uvioresistant PET fiber and preparation method thereof
CN108893798A (en) * 2018-06-11 2018-11-27 浙江华基环保科技有限公司 A kind of uvioresistant fiber, the fibrous filter net and its preparation method and application

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1147033A (en) * 1996-08-16 1997-04-09 刘明然 Ultraviolet screening mother granule and fiber
CN1357650A (en) * 2000-12-07 2002-07-10 天津市发博纺织材料有限责任公司 Jinlun-6 uvioresistant fiber and its production process
US20040074012A1 (en) * 2001-02-06 2004-04-22 Thomas Heidenfelder Method for providing textile material with uv protection
CN1896347A (en) * 2006-04-10 2007-01-17 东华大学 Anti-ultraviolet superfine terylene and its preparation

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1147033A (en) * 1996-08-16 1997-04-09 刘明然 Ultraviolet screening mother granule and fiber
CN1357650A (en) * 2000-12-07 2002-07-10 天津市发博纺织材料有限责任公司 Jinlun-6 uvioresistant fiber and its production process
US20040074012A1 (en) * 2001-02-06 2004-04-22 Thomas Heidenfelder Method for providing textile material with uv protection
CN1896347A (en) * 2006-04-10 2007-01-17 东华大学 Anti-ultraviolet superfine terylene and its preparation

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
具本植等: "抗氧剂双(3,5-二叔丁基-4-羟基苄基膦酸单乙酯)钙盐的合成", 《精细石油化工》 *
吴建华: "抗紫外纤维及其织物的加工技术", 《合成纤维》 *

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103469559A (en) * 2013-08-21 2013-12-25 昆山铁牛衬衫厂 UV-resistant composite finishing agent and preparation method thereof
CN107059159A (en) * 2017-05-19 2017-08-18 江苏华昌织物有限公司 A kind of preparation method of anti-aging shading screen cloth
CN107200981A (en) * 2017-07-19 2017-09-26 成都新柯力化工科技有限公司 A kind of antiultraviolet plastic matrix and preparation method
CN107200981B (en) * 2017-07-19 2019-06-11 浙江乍浦塑料制品有限公司 A kind of antiultraviolet plastic matrix and preparation method
CN107604458A (en) * 2017-10-31 2018-01-19 上海稀美师塑料着色科技有限公司 A kind of preparation method of durable uvioresistant polypropylene fibre
CN107604458B (en) * 2017-10-31 2022-01-07 稀美师新材料科技(常州)有限公司 Preparation method of durable ultraviolet-resistant polypropylene fiber
CN108456947A (en) * 2018-01-12 2018-08-28 浙江东太新材料有限公司 A kind of uvioresistant PET fiber and preparation method thereof
CN108456947B (en) * 2018-01-12 2020-06-05 浙江东太新材料有限公司 Anti-ultraviolet PET fiber and preparation method thereof
CN108893798A (en) * 2018-06-11 2018-11-27 浙江华基环保科技有限公司 A kind of uvioresistant fiber, the fibrous filter net and its preparation method and application

Similar Documents

Publication Publication Date Title
JP6722256B2 (en) Polyethylene terephthalate fiber containing plant extract
CN102851942A (en) Anti-ultraviolet pure cotton fabric finishing method
CN102851766A (en) Anti-ultraviolet fiber production method
CN109505024B (en) Antibacterial ultraviolet-proof fabric and preparation method thereof
CN102851773A (en) Production method of uvioresistant fiber
CN103469557A (en) Method for finishing ultraviolet-proof antibacterial fabric
CN103469556A (en) Ultraviolet-proof antibacterial finishing agent
CN101871139A (en) Far infrared anionic magnetic fiber and manufacturing method thereof
CN102828396A (en) Production method of uvioresistant full-cotton shirts
CN109137535A (en) A kind of preparation method for adding china-hemp fibers powder-nano material heat insulation and heat control type wear-resistant uvioresistant line umbrella cloth
CN106319685A (en) Heat insulation core-shell composite fiber for reflecting near infrared rays, and production method of fiber
CN107012524B (en) A kind of uvioresistant function fiber producing processes based on organic synthesis
CN1057809C (en) Anti-ultraviolet ray cool and health fabric and it producing method
CN102453969A (en) Artificial cotton containing nanometer material
CN106676665B (en) A kind of antiultraviolet nylon stretch yarn
CN110144650B (en) Multifunctional pearl polylactic acid blended yarn and preparation method thereof
CN110241622B (en) Anti-ultraviolet polyester fabric
CN103469558A (en) Method for preparing ultraviolet-proof antibacterial finishing agent
CN116397440A (en) A micro-food containing probiotics functional plant fiber of capsule
CN102851772A (en) Masterbatch method for manufacturing heat-storing temperature-regulating fiber
CN107364203B (en) A kind of radiation-proof fabric and its production method
CN106510060A (en) Luminous fabric based on silicate and preparation method of fabric
CN102704142A (en) Zirconium nano composite functional tencel fabric and weaving, dyeing and finishing process and application thereof
CN103469560A (en) Finishing method of UV-resistant pure cotton fabrics
CN102691206B (en) Tourmaline-containing cloth and production process thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20130102