CN103374764B - Pearl anti-ultraviolet fiber and preparation method thereof - Google Patents

Pearl anti-ultraviolet fiber and preparation method thereof Download PDF

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Publication number
CN103374764B
CN103374764B CN201210133290.8A CN201210133290A CN103374764B CN 103374764 B CN103374764 B CN 103374764B CN 201210133290 A CN201210133290 A CN 201210133290A CN 103374764 B CN103374764 B CN 103374764B
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Prior art keywords
ultraviolet
fiber
pearl anti
ultraviolet fiber
resistance
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Expired - Fee Related
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CN201210133290.8A
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CN103374764A (en
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宋国新
黄毅
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Jiangyin Xiangyang special chemical fiber Co., Ltd.
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Shanghai Taohong Chemical Technology Co Ltd
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Abstract

The invention discloses a kind of Pearl anti-ultraviolet fiber and preparation method thereof, described Pearl anti-ultraviolet fiber is prepared from by following step: join in viscose solution by UV resistance functional latex, mix homogeneously, filter, wet spinning spinning process molding routinely, the mass ratio obtaining the Pearl anti-ultraviolet fiber of the present invention, described UV resistance functional latex and viscose solution is 2: 100~5: 100, described UV resistance functional latex, is made up of by weight following component: Margarita powder 20-30 part; Isononyl isononanoate 1-3 part; UV resistance agent 0.2-0.4 part; Palmitamide CAB 10-15 part; 1-isobutyl-3,5-dimethylhexylphosphoric acid potassium salt 5-10 part; Tween-60? 20-25 part; Water 100-200 part. The Pearl anti-ultraviolet fiber of the present invention, outward appearance has silkiness gloss, and preventing ultraviolet effect is notable.

Description

Pearl anti-ultraviolet fiber and preparation method thereof
Technical field
The present invention relates to a kind of viscose rayon and preparation method thereof, particularly relate to a kind of Pearl anti-ultraviolet fiber and preparation method thereof.
Background technology
Viscose rayon (viscosefibre), is viscous fine full name. It is divided into again viscose filament yarn and short rayon fiber. The cellulose fibre that viscous fibre is is raw material production with cotton or other natural fiber. In 12 kinds of main textile fabrics, viscous fine moisture percentage meets the physiological requirement of human body skin most, has the characteristics such as smooth nice and cool, ventilative, antistatic, dyeing is gorgeous.
Viscose rayon belongs to regenerated celulose fibre. It is with native cellulose for raw material, makes soluble cellulose sulphonic acid ester through operations such as alkalization, aging, sulfonation, is re-dissolved in sig water and makes viscose glue, make through wet spinning. Adopt different raw materials and spinning technique, it is possible to respectively obtain common viscose fiber, koplon and high tenacity staple fibre etc. Common viscose fiber has general physical and mechanical properties and chemical property, divides again cotton, wool type and long filament type, is commonly called as synthetic cotton, man-made hair and artificial silk.
Viscous fibre is one of ancient fiber species. 1891, Kroes, Buddhist script written on pattra leaves and be first made for sodium cellulose xanghate solution with cotton for raw material than Dare, owing to the viscosity of this solution is very big, thus name " viscose glue ". After acid met by viscose glue, cellulose precipitates out again. According to this principle, within 1893, developing into a kind of method manufacturing cellulose fibre, this fiber is just called " viscose rayon ". By 1905, Miller that etc. invented dilute sulfuric acid and the coagulating bath of sulfate composition, it is achieved that the industrialized production of viscose rayon.
The basic composition of viscose rayon is cellulose. The cross section indention skin-core structure of common viscose fiber, longitudinally straight have ditch horizontal. And rich fine without skin-core structure, cross section is rounded.
Viscose rayon has good hygroscopicity, and when general atmosphere, regain is about 13%. Significantly expanding after moisture absorption, diameter increases up to 50%, so after water, feel is hardened under fabric, shrinkage factor is big. The fracture strength of common viscose fiber is less than cotton, is about 1.6~2.7cN/dtex; Elongation at break, more than cotton, is 16%~22%; Wet strong declining many, be about dry strong by 50%, hygrometric state elongation increases about 50%.
The chemical composition of viscose rayon is similar to cotton, thus more alkaline-resisting and not acidproof, but all more cotton difference of alkaline-resisting acid resistance. In addition the thermal property of viscose rayon is also similar to cotton, and density is 1.50~1.52g/cm close to cotton3. The hydroxyl of cellulosic macromole is prone to multiple chemical reaction, therefore, can pass through the methods such as grafting, viscose rayon is modified, improve viscose rayon performance, and produce the fiber of various specific use.
But, existing viscose rayon, due to function singleness, is not increasingly approved by market. Therefore, urgently it is desirable to develop high performance industry function viscose fiber, promotes the surcharge of viscose rayon, to meet the needs of people's increasingly diversification.
Summary of the invention
In order to solve prior art above shortcomings, the preparation method that one of the technical problem to be solved is to provide a kind of Pearl anti-ultraviolet fiber.
The two of the technical problem to be solved are to provide above-mentioned Pearl anti-ultraviolet fiber.
Technical scheme, is achieved in that
The preparation method of Pearl anti-ultraviolet fiber, is made up of following step:
UV resistance functional latex is joined in viscose solution, mix homogeneously, filter, wet spinning spinning process molding routinely, the mass ratio obtaining the Pearl anti-ultraviolet fiber of the present invention, described UV resistance functional latex and viscose solution is 2: 100~5: 100;
Wherein, described UV resistance functional latex, it is made up of by weight following component: Margarita powder 20-30 part; Isononyl isononanoate 1-3 part; UV resistance agent 0.2-0.4 part; Palmitamide CAB 10-15 part; 1-isobutyl-3,5-dimethylhexylphosphoric acid potassium salt 5-10 part; Tween-60 20-25 part; Water 100-200 part.
Margarita powder, isononyl isononanoate, UV resistance agent, palmitamide CAB, 1-isobutyl-3,5-dimethylhexylphosphoric acid potassium salt and Tween-60 are uniformly mixed, after ball mill ball milling 3-5 hour, add water, be stirred for mix homogeneously, can be prepared by this UV resistance functional latex.
The particle diameter of described Margarita powder is 50-300 nanometer, it is preferred to 50-100 nanometer.
Described UV resistance agent is ESCALOL 567, 2-(2 '-hydroxyl-5 '-aminomethyl phenyl) benzotriazole, 2,4,6-tri-(2 '-hydroxyl, 4 '-n-butoxyphenyl), 2-(2 '-hydroxyl-3 '-tertiary butyl-5 '-aminomethyl phenyl)-5-chlorobenzotriazole, 2,2 '-(Isosorbide-5-Nitrae-phenylene) double, two-4H-3,1-benzoxazin-4-ones, 2,4-dihydroxy benzophenone, ESCALOL 567, Octabenzone, 2-(2 '-hydroxyl-5 '-aminomethyl phenyl) benzotriazole, azo-bis-iso-dimethyl, 2-(4,6-double, two (2,4-3,5-dimethylphenyl)-1,3,5-triazines-2-bases)-5-octyloxy phenol, 2-hydroxyl-4-dodecyloxy benzophenones, 2-(2 '-hydroxyl-5 '-t-octyl phenyl) benzotriazole, 2 '-(2 '-hydroxyl-3 '-tert-butyl group-5 '-aminomethyl phenyl)-5-chlorobenzotriazoles, 2-(2 '-hydroxyl-3 ', 5 '-di-tert-butyl-phenyl)-benzotriazole, 2-(2 '-hydroxyl-3 ', 5 '-di-tert-butyl-phenyl)-5-chlorinated benzotriazole, 2-hydroxyl-4-methoxybenzophenone-5-sulfonic acid, 2,2-thiobiss (4-tert-octyl phenol) n-butylamine nickel salt, 2-(2 '-hydroxyl-3 ', 5 '-diamyl phenyl) benzotriazole, N-(2-ethoxyl phenenyl)-N '-(4-ethylphenyl)-oxalamide, 2-(2 '-hydroxyl-3 ', 5 '-di-tert-pentyl-phenyl) benzotriazole, 2-PHENYLBENZIMIDAZOLE-5-SULFONIC ACID, 2-(2 '-hydroxyl-3 '-isobutyl group-5 '-tert-butyl-phenyl) benzotriazole, N-(carboethoxyphenyl)-N '-methyl-N '-phenyl formamidine, N-(carboethoxyphenyl)-N '-ethyl-N '-phenyl formamidine, 2-(2H-benzotriazole-2)-4,6-bis-(1-methyl isophthalic acid-phenylethyl) phenol, 2-(2H-benzotriazole-2-base)-6-(1-methyl isophthalic acid-phenethyl)-4-(1,1,3,3-tetramethyl butyl) phenol, 2,2 '-di-2-ethylhexylphosphine oxide (4-t-octyl-6-benzotriazole phenol), double, two { 3-[3-(2H-benzotriazole-2-base)-4-hydroxyl-5-tert-butyl-phenyl]-propanoic acid }-Liquid Macrogol ester, 3-[3-(2-H-benzotriazole-2-base)-4-hydroxyl-5-tert-butyl-phenyl]-propanoic acid-Liquid Macrogol ester, 2-(2H-benzotriazole-2-base)-6-dodecyl-4-cresol, 2-(4,6-diphenyl-1,3,5-triazines-2-base)-5-hexyl oxygen base-phenol, (1-hydroxy-cyclohexyl) [4-(2-hydroxyl-oxethyl) phenyl] ketone, 2 hydroxybenzoic acid-4-(1,1-dimethyl ethyl) phenylester and 4,4 ', 4 " one in-(1,3,5-triazines-2,4,6-tri-imino groups) three benzoic acid three (2-ethylhexyl) ester or its mixture.
In the present invention, described viscose solution, refer to the sodium hydrate aqueous solution of cellulose sulfonate, it is the intermediate raw material that the industry is general.
Preferably, in described viscose solution, the weight percent content of first fibre is 8-9%, and the weight percent content of alkali is 4-6%, the falling ball viscosity 45-65 second, degree of ripeness 8-16%.
Preferably, adopting filter to be filtered, its filtering accuracy is≤4 μm.
Present invention also offers a kind of Pearl anti-ultraviolet fiber, adopt said method to be prepared from.
Relative to prior art, beneficial effects of the present invention is embodied as: the Pearl anti-ultraviolet fiber of the present invention, and outward appearance has silkiness gloss, and preventing ultraviolet effect is notable. The Pearl anti-ultraviolet fiber good spinnability of the present invention, can with fibrous woven raw material blending such as cotton, tencel, Modal, cashmere, real silks.
Detailed description of the invention
Embodiment 1
(1) preparation of UV resistance functional latex
Margarita powder 30 kilograms; Isononyl isononanoate 1 kilogram; UV resistance agent UV-P0.4 kilogram; Palmitamide CAB 10 kilograms; 1-isobutyl-3,5-dimethylhexylphosphoric acid potassium salt 10 kilograms; Tween-60 20 kilograms; 200 kilograms of water.
Described UV resistance agent UV-P, also known as Ultraviolet Absorber UV-P, chemical name is: 2-(2 '-hydroxyl-5 '-aminomethyl phenyl) benzotriazole.
Margarita powder, isononyl isononanoate, UV resistance agent, palmitamide CAB, 1-isobutyl-3,5-dimethylhexylphosphoric acid potassium salt and Tween-60 are uniformly mixed, after ball mill ball milling 3 hours, add water, be stirred for mix homogeneously, can be prepared by this UV resistance functional latex.
(2) preparation of Pearl anti-ultraviolet fiber
UV resistance functional latex is joined in viscose solution, mix homogeneously, filters, wherein filtering accuracy is≤4 μm, wet spinning spinning process molding routinely, the mass ratio obtaining the Pearl anti-ultraviolet fiber of the present invention, described UV resistance functional latex and viscose solution is 5: 100.
In described viscose solution, the weight percent content of first fibre is 8%, and the weight percent content of alkali is 6%, falling ball viscosity 45 seconds, degree of ripeness 16%.
The Pearl anti-ultraviolet fiber dyeability of the present invention is good, and color dye is bright-coloured, and the acid of routine, alkali post processing can't affect performance and the nutritional labeling of Pearl anti-ultraviolet fiber. The Pearl anti-ultraviolet fiber adding natural peral contains several amino acids specific to Margarita and trace element, and these nutrients are meeting dissolution gradually under human body skin sour environment long term, nourishes human skin.
Comparative example 1:
Being filtered by viscose solution, the molding of wet spinning spinning process, obtains viscose rayon routinely.
In described viscose solution, the weight percent content of first fibre is 8%, and the weight percent content of alkali is 6%, falling ball viscosity 45 seconds, degree of ripeness 16%.
Embodiment 2
(1) preparation of UV resistance functional latex
Margarita powder 20 kilograms; Isononyl isononanoate 3 kilograms; UV resistance agent triazine-50.2 kilograms; Palmitamide CAB 15 kilograms; 1-isobutyl-3,5-dimethylhexylphosphoric acid potassium salt 5 kilograms; Tween-60 25 kilograms; 100 kilograms of water.
Described UV resistance agent triazine-5, also known as UV absorbent triazine-5, chemical name: 2,4,6-tri-(2 '-hydroxyl, 4 '-n-butoxyphenyl).
Margarita powder, isononyl isononanoate, UV resistance agent, palmitamide CAB, 1-isobutyl-3,5-dimethylhexylphosphoric acid potassium salt and Tween-60 are uniformly mixed, after ball mill ball milling 5 hours, add water, be stirred for mix homogeneously, can be prepared by this UV resistance functional latex.
(2) preparation of Pearl anti-ultraviolet fiber
UV resistance functional latex is joined in viscose solution, mix homogeneously, filters, wherein filtering accuracy is≤3 μm, wet spinning spinning process molding routinely, the mass ratio obtaining the Pearl anti-ultraviolet fiber of the present invention, described UV resistance functional latex and viscose solution is 2: 100.
In described viscose solution, the weight percent content of first fibre is 9%, and the weight percent content of alkali is 4%, falling ball viscosity 65 seconds, degree of ripeness 8%.
The Pearl anti-ultraviolet fiber dyeability of the present invention is good, and color dye is bright-coloured, and the acid of routine, alkali post processing can't affect performance and the nutritional labeling of Pearl anti-ultraviolet fiber. The Pearl anti-ultraviolet fiber adding natural peral contains several amino acids specific to Margarita and trace element, and these nutrients are meeting dissolution gradually under human body skin sour environment long term, nourishes human skin.
Test case 1
Project Embodiment 1 Comparative example 1
Fineness of yarn, tex 18 18
Average ultimate strength, CN 282 286
Ultimate strength coefficient of variation CV, % 5.11 5.18
Average extension at break, % 8.6 9.1
Extension at break coefficient of variation CV, % 10.22 10.32
Yarn strength, CN/tex 15.48 16.33
Average regain, % 12.23 12.01
Area shrinkage, % 26.2 29.3
Breathability, L/m2s 962 732
The visible present invention is identical with common viscose fiber Fundamental Physical Properties, does not die down because with the addition of functional additive Margarita powder, and breathability, area shrinkage are effectively improved simultaneously.
Test case 2
Reference standard GB/T18830-2002, carries out the performance test of fabric protective solar UV.
Project Embodiment 1 Embodiment 2
Ultraviolet ray transmissivity UVB, % 1.3 1.8
Ultraviolet ray transmissivity UVA, % 1.2 1.6
UPF UPF 80 70
As the UPF > 30 of sample, and the transmitance of UVA less than 5% time, can be described as anti-ultraviolet product. Visible, the present invention has fabulous ultraviolet resistance.
Margarita powder, isononyl isononanoate and the composite use of UV resistance agent, join in viscose rayon in the present invention, creates active and effective effect, and prepared Pearl anti-ultraviolet fiber preventing ultraviolet effect is notable.

Claims (5)

1. the preparation method of Pearl anti-ultraviolet fiber, it is characterised in that be made up of following step:
UV resistance functional latex is joined in viscose solution, mix homogeneously, filter, wet spinning spinning process molding routinely, the mass ratio of described UV resistance functional latex and viscose solution is 2:100~5:100;
Described UV resistance functional latex is made up of by weight following component:
Margarita powder 20-30 part; Isononyl isononanoate 1-3 part; UV resistance agent 0.2-0.4 part; Palmitamide CAB 10-15 part; 1-isobutyl-3,5-dimethylhexylphosphoric acid potassium salt 5-10 part; Tween-60 20-25 part; Water 100-200 part;
The particle diameter of described Margarita powder is 50-300 nanometer.
2. the preparation method of Pearl anti-ultraviolet fiber as claimed in claim 1, it is characterised in that the particle diameter of described Margarita powder is 50-100 nanometer.
3. the preparation method of Pearl anti-ultraviolet fiber as claimed in claim 1, it is characterized in that, described UV resistance functional latex adopts following method to be prepared from: Margarita powder, isononyl isononanoate, UV resistance agent, palmitamide CAB, 1-isobutyl-3,5-dimethylhexylphosphoric acid potassium salt and Tween-60 are uniformly mixed, after ball mill ball milling 3-5 hour, add water, be stirred for mix homogeneously.
4. the preparation method of the Pearl anti-ultraviolet fiber as according to any one of claim 1-3, it is characterized in that: in described viscose solution, the weight percent content of first fibre is 8-9%, and the weight percent content of alkali is 4-6%, the falling ball viscosity 45-65 second, degree of ripeness 8-16%.
5. Pearl anti-ultraviolet fiber, it is characterised in that: adopt the method according to any one of claim 1-4 to be prepared from.
CN201210133290.8A 2012-04-28 2012-04-28 Pearl anti-ultraviolet fiber and preparation method thereof Expired - Fee Related CN103374764B (en)

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CN103911857B (en) * 2014-03-24 2016-03-09 灵山县桂合丝业有限公司 A kind of production method of anti-yellowing anti-bacteria real silk quilt cover
KR20160142389A (en) * 2014-04-08 2016-12-12 스마트폴리머 게엠베하 Shaped cellulose bodies with physiologically active mineral substances distributed therein
CN104313719A (en) * 2014-11-04 2015-01-28 常熟市新达纬编厂 Uvioresistant fiber
CN105002589A (en) * 2015-05-20 2015-10-28 铜陵宏正网络科技有限公司 Natural skin care uvioresistant cashmere complex fiber containing pearl fibers and manufacturing method thereof
CN107605387B (en) * 2017-08-17 2020-10-30 东华大学 Ultraviolet-proof nanofiber composite screen window and preparation method thereof
CN109023076A (en) * 2018-09-05 2018-12-18 合肥久新不锈钢厨具有限公司 A kind of stainless steel and preparation method thereof with anti-ultraviolet function
CN113005551A (en) * 2021-03-08 2021-06-22 镧明材料技术(上海)有限公司 Rare earth-added ultraviolet-resistant anti-aging viscose fiber and preparation method thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1337479A (en) * 2000-08-05 2002-02-27 吉林化纤集团高科技开发有限公司 Unioresistant viscose fibre producing process
CN101245498A (en) * 2008-03-14 2008-08-20 唐山三友兴达化纤股份有限公司 Shell powder viscose fiber and method for manufacturing same
CN101328646A (en) * 2008-06-20 2008-12-24 东华大学 Preparation of ultravioresistant nonwoven
CN101487149A (en) * 2009-02-20 2009-07-22 苏州恒光化纤有限公司 Method for producing pearl protein cellulose fibre
CN101532184A (en) * 2009-03-28 2009-09-16 山东海龙股份有限公司 Pearl regenerated cellulose fiber and preparation method thereof

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3769155B2 (en) * 1999-10-07 2006-04-19 大和紡績株式会社 Cationic dye dyeable viscose rayon

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1337479A (en) * 2000-08-05 2002-02-27 吉林化纤集团高科技开发有限公司 Unioresistant viscose fibre producing process
CN101245498A (en) * 2008-03-14 2008-08-20 唐山三友兴达化纤股份有限公司 Shell powder viscose fiber and method for manufacturing same
CN101328646A (en) * 2008-06-20 2008-12-24 东华大学 Preparation of ultravioresistant nonwoven
CN101487149A (en) * 2009-02-20 2009-07-22 苏州恒光化纤有限公司 Method for producing pearl protein cellulose fibre
CN101532184A (en) * 2009-03-28 2009-09-16 山东海龙股份有限公司 Pearl regenerated cellulose fiber and preparation method thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
珍珠粘胶纤维的性能及产品开发;赵博;《江苏丝绸》;20110815(第4期);第32-34页 *

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