CN104277469A - Wood fiber capable of radiating far-infrared rays and manufacturing method thereof - Google Patents
Wood fiber capable of radiating far-infrared rays and manufacturing method thereof Download PDFInfo
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- CN104277469A CN104277469A CN201410454661.1A CN201410454661A CN104277469A CN 104277469 A CN104277469 A CN 104277469A CN 201410454661 A CN201410454661 A CN 201410454661A CN 104277469 A CN104277469 A CN 104277469A
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- 229920002522 Wood fibre Polymers 0.000 title abstract description 7
- 239000002025 wood fiber Substances 0.000 title abstract description 7
- 238000004519 manufacturing process Methods 0.000 title abstract description 3
- 239000000835 fiber Substances 0.000 claims abstract description 42
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 14
- 238000000034 method Methods 0.000 claims abstract description 12
- 239000000843 powder Substances 0.000 claims abstract description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 11
- 229920000742 Cotton Polymers 0.000 claims abstract description 10
- 239000000919 ceramic Substances 0.000 claims abstract description 9
- 239000004793 Polystyrene Substances 0.000 claims abstract description 7
- 229920000297 Rayon Polymers 0.000 claims abstract description 7
- 240000000111 Saccharum officinarum Species 0.000 claims abstract description 7
- 235000007201 Saccharum officinarum Nutrition 0.000 claims abstract description 7
- 244000269722 Thea sinensis Species 0.000 claims abstract description 7
- XQBCVRSTVUHIGH-UHFFFAOYSA-L [dodecanoyloxy(dioctyl)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCCCCCC)(CCCCCCCC)OC(=O)CCCCCCCCCCC XQBCVRSTVUHIGH-UHFFFAOYSA-L 0.000 claims abstract description 7
- 239000004203 carnauba wax Substances 0.000 claims abstract description 7
- 235000013869 carnauba wax Nutrition 0.000 claims abstract description 7
- 239000002105 nanoparticle Substances 0.000 claims abstract description 7
- 229920002223 polystyrene Polymers 0.000 claims abstract description 7
- 239000002994 raw material Substances 0.000 claims abstract description 7
- 229940089401 xylon Drugs 0.000 claims description 24
- -1 polyethylene Polymers 0.000 claims description 21
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 claims description 12
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 12
- 238000003756 stirring Methods 0.000 claims description 12
- 230000008569 process Effects 0.000 claims description 9
- 230000005855 radiation Effects 0.000 claims description 9
- 239000003063 flame retardant Substances 0.000 claims description 7
- 230000004048 modification Effects 0.000 claims description 7
- 238000012986 modification Methods 0.000 claims description 7
- 238000002360 preparation method Methods 0.000 claims description 7
- 229940100555 2-methyl-4-isothiazolin-3-one Drugs 0.000 claims description 6
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims description 6
- 241000628997 Flos Species 0.000 claims description 6
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 claims description 6
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 6
- 239000004698 Polyethylene Substances 0.000 claims description 6
- 240000007164 Salvia officinalis Species 0.000 claims description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 6
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 6
- 239000012752 auxiliary agent Substances 0.000 claims description 6
- 239000002131 composite material Substances 0.000 claims description 6
- 239000013256 coordination polymer Substances 0.000 claims description 6
- 239000004205 dimethyl polysiloxane Substances 0.000 claims description 6
- 238000001035 drying Methods 0.000 claims description 6
- 230000009977 dual effect Effects 0.000 claims description 6
- 239000012467 final product Substances 0.000 claims description 6
- 229940075507 glyceryl monostearate Drugs 0.000 claims description 6
- 238000000227 grinding Methods 0.000 claims description 6
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 6
- 229960004232 linoleic acid Drugs 0.000 claims description 6
- BEGLCMHJXHIJLR-UHFFFAOYSA-N methylisothiazolinone Chemical compound CN1SC=CC1=O BEGLCMHJXHIJLR-UHFFFAOYSA-N 0.000 claims description 6
- 239000003595 mist Substances 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 6
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 claims description 6
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims description 6
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 6
- 229920000573 polyethylene Polymers 0.000 claims description 6
- 238000010298 pulverizing process Methods 0.000 claims description 6
- 235000005412 red sage Nutrition 0.000 claims description 6
- 150000003376 silicon Chemical class 0.000 claims description 6
- 239000011863 silicon-based powder Substances 0.000 claims description 6
- 238000013019 agitation Methods 0.000 claims description 3
- 238000009835 boiling Methods 0.000 claims description 3
- 239000007795 chemical reaction product Substances 0.000 claims description 3
- 238000004537 pulping Methods 0.000 claims description 3
- 238000005507 spraying Methods 0.000 claims description 3
- 241000894006 Bacteria Species 0.000 abstract description 2
- 241000196324 Embryophyta Species 0.000 abstract description 2
- 241001465754 Metazoa Species 0.000 abstract description 2
- 230000008901 benefit Effects 0.000 abstract description 2
- 230000003915 cell function Effects 0.000 abstract description 2
- 230000008929 regeneration Effects 0.000 abstract description 2
- 238000011069 regeneration method Methods 0.000 abstract description 2
- 230000002708 enhancing effect Effects 0.000 abstract 2
- 240000008107 Arenga engleri Species 0.000 abstract 1
- 235000004019 Arenga engleri Nutrition 0.000 abstract 1
- 241000218176 Corydalis Species 0.000 abstract 1
- 206010061218 Inflammation Diseases 0.000 abstract 1
- 230000003467 diminishing effect Effects 0.000 abstract 1
- 230000001900 immune effect Effects 0.000 abstract 1
- 230000004054 inflammatory process Effects 0.000 abstract 1
- 235000021190 leftovers Nutrition 0.000 abstract 1
- 230000001737 promoting effect Effects 0.000 abstract 1
- 238000011084 recovery Methods 0.000 abstract 1
- 230000008961 swelling Effects 0.000 abstract 1
- 210000002268 wool Anatomy 0.000 abstract 1
- 239000000047 product Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- 241000222122 Candida albicans Species 0.000 description 1
- 241000191967 Staphylococcus aureus Species 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 229940095731 candida albicans Drugs 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000011094 fiberboard Substances 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 210000002865 immune cell Anatomy 0.000 description 1
- 230000000968 intestinal effect Effects 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
The invention discloses a wood fiber capable of radiating far-infrared rays, which is characterized by comprising the following raw materials in parts by weight: 40-44 parts of wood fiber, 7-9 parts of fine wool cotton fiber, 5-8 parts of viscose fiber, 6-10 parts of Arenga engleri Beccari fiber, 20-25 parts of sugarcane peel, 17-19 parts of tea leftovers, 1-3 parts of infrared ceramic powder, 1.2-2.5 parts of polystyrene nanoparticle, 4-7 parts of carnauba wax, 10-13 parts of ethanol, 4-8 parts of polyvinylacetal, 0.3-0.7 part of dioctyltin dilaurate, 3-4 parts of markka, 2-4 parts of corydalis tuber, 1-2 parts of radix salviae miltiorrhizae, 3-6 parts of assistant and a right amount of water. By optimizing the production technique and adding the infrared ceramic powder, the wood fiber can radiate far-infrared rays, and has the advantages of diminishing inflammation, promoting the subsidence of swelling, resisting bacteria, enhancing the cell regeneration capacity and immunological cell functions and the like when acting on the human body. Besides, the multiple animal and plant fibers are added and mutually compounded, thereby saving the cost and enhancing the characteristics of the wood fiber. The prepared wood fiber is widely used in the fields of medical treatment and recovery.
Description
Technical field
The present invention relates to a kind of xylon modification field, be specifically related to radiation infrared xylon of a kind of energy and preparation method thereof.
Background technology
Pure natural wood fiber product is the same with cotton be all 100% green product, there is natural antibiotic health care, remove peculiar smell, from self-cleaning clearly function, soft-touch, does not harden hardening, is the healthy products of real, a pure green.Therefore the extremely popular favor of pure natural xylon, is widely used in the fields such as towel, underwear, T-shirt, kitchen towel, socks, shirt, Western-style clothes, baby's textiles, bedclothes, curtain, fabric, bedding and padding.
In prior art, xylon is inflammable exists many weak points: because xylon has the water absorbability more superior than cotton fibre and ventilation property, therefore apt to rot time for being processed into fiberboard, easy conductive, inflammable etc., and xylon is compared to comparatively hard for quality time knitting cotton fibre, sense of touch is poor; Secondly, because time prepared by xylon, starting material are limited, and existing life multiple demands etc. cannot be met, so xylon is restricted in its use range of a very long time.
Summary of the invention
Object of the present invention is just to provide radiation infrared xylon of a kind of energy and preparation method thereof, to overcome the deficiencies in the prior art.
The object of the present invention is achieved like this:
The xylon that a kind of energy is radiation infrared, it is characterized in that, be made up of the raw material of following weight part: xylon 40-44, medium staple cotton fiber 7-9, viscose fiber 5-8, mountain palm fibre fiber 6-10, Sugarcane peel. 20-25, tea rim charge 17-19, infrared ceramic powder 1-3, polystyrene nanoparticles 1.2-2.5, carnauba wax 4-7, ethanol 10-13, polyvinylacetal 4-8, Bis(lauroyloxy)dioctyltin 0.3-0.7, agate card 3-4, Yanhusuo 2-4, red sage root 1-2, auxiliary agent 3-6, suitable quantity of water.
Described auxiliary agent is made up of following raw materials in part by weight: tealeaves fiber 10-13, nano zine oxide 2-4, silicon powder 1-3, dual polyethylene polydimethylsiloxane 0.03-0.05, glyceryl monostearate 1.2-3.1, polyoxyethylene glycol 3-6, methylisothiazolinone 2.1-3.6, Oleum Pelargonii Graveolentis 3.2-4.7, Flos Pelargonii Hortori 0.2-0.4, linolic acid 1.3-2.4, Dyhard RU 100 0.1-0.2, ethyl acrylate 4-7, fire retardant CP 0.04-0.07, its preparation method be first by nano zine oxide ultrasonic disperse in polyoxyethylene glycol, add tealeaves blending in of fibers and stir 5-8 hour, take out drying and grinding 10-15 minute, obtained modification tealeaves fiber, then by Oleum Pelargonii Graveolentis, Flos Pelargonii Hortori adds water stirring, and add silicon powder and stir 30-40 minute, spraying dry obtains modified silicon micro mist, finally by ethyl acrylate, linolic acid, Dyhard RU 100, methylisothiazolinone stirring and evenly mixing, adds above-mentioned obtained modification tealeaves fiber and modified silicon micro mist, glyceryl monostearate, dual polyethylene polydimethylsiloxane, fire retardant CP supersound process 30-40 minute and get final product.
The preparation method of the xylon that described a kind of energy is radiation infrared, is characterized in that comprising the following steps:
(1) add water after getting Sugarcane peel., tea rim charge, agate card, Yanhusuo, the red sage root pulverizing boiling pulping, adds infrared ceramic powder agitation grinding 20-30 minute, send in defibrator and be processed into modified composite fiber;
(2) by ethanol, polyvinylacetal heated and stirred, carnauba wax, polystyrene nanoparticles, Bis(lauroyloxy)dioctyltin supersound process 20-40 minute is added;
(3) xylon, medium staple cotton fiber, viscose fiber, mountain palm fibre fiber, modified composite fiber are put into pulverizing mill and worn into 80-100 order powder, putting into high mixer after drying mixes to 80-90 DEG C, add step (2) reaction product and remaining component is mixed to 100-120 DEG C, leave standstill supersound process 10-15 minute after 15-20 hour, wash, filter, dry to constant weight and get final product.
The present invention has following beneficial effect: optimized production process of the present invention adds infrared ceramic powder, can be radiation infrared, there is heat effect, act on human body and there is anti-inflammatory, detumescence, antibacterial, advantage such as raising cell regeneration ability and immune cell function etc., in addition the present invention also adds the mutual compound of multiple animal and plant fiber, the cost-saving characteristic simultaneously also improving xylon, obtained xylon is widely used at medical treatment, rehabilitation field.
Embodiment
The xylon that described a kind of energy is radiation infrared, it is characterized in that, be made up of the raw material of following weight part: xylon 43, medium staple cotton fiber 9, viscose fiber 7, mountain palm fibre fiber 8, Sugarcane peel. 21, tea rim charge 17, infrared ceramic powder 1, polystyrene nanoparticles 1.8, carnauba wax 4, ethanol 13, polyvinylacetal 4, Bis(lauroyloxy)dioctyltin 0.3, agate card 3, Yanhusuo 2, the red sage root 2, auxiliary agent 6, suitable quantity of water.
Described auxiliary agent is made up of following raw materials in part by weight: tealeaves fiber 12, nano zine oxide 2, silicon powder 1, dual polyethylene polydimethylsiloxane 0.05, glyceryl monostearate 1.9, polyoxyethylene glycol 4, methylisothiazolinone 2.8, Oleum Pelargonii Graveolentis 4.5, Flos Pelargonii Hortori 0.3, linolic acid 1.9, Dyhard RU 100 0.1, ethyl acrylate 4, fire retardant CP 0.07, its preparation method be first by nano zine oxide ultrasonic disperse in polyoxyethylene glycol, add tealeaves blending in of fibers and stir 5-8 hour, take out drying and grinding 10-15 minute, obtained modification tealeaves fiber, then by Oleum Pelargonii Graveolentis, Flos Pelargonii Hortori adds water stirring, and add silicon powder and stir 30-40 minute, spraying dry obtains modified silicon micro mist, finally by ethyl acrylate, linolic acid, Dyhard RU 100, methylisothiazolinone stirring and evenly mixing, adds above-mentioned obtained modification tealeaves fiber and modified silicon micro mist, glyceryl monostearate, dual polyethylene polydimethylsiloxane, fire retardant CP supersound process 30-40 minute and get final product.
Making method comprises the following steps:
(1) add water after getting Sugarcane peel., tea rim charge, agate card, Yanhusuo, the red sage root pulverizing boiling pulping, adds infrared ceramic powder agitation grinding 20-30 minute, send in defibrator and be processed into modified composite fiber;
(2) by ethanol, polyvinylacetal heated and stirred, carnauba wax, polystyrene nanoparticles, Bis(lauroyloxy)dioctyltin supersound process 20-40 minute is added;
(3) xylon, medium staple cotton fiber, viscose fiber, mountain palm fibre fiber, modified composite fiber are put into pulverizing mill and worn into 80-100 order powder, putting into high mixer after drying mixes to 80-90 DEG C, add step (2) reaction product and remaining component is mixed to 100-120 DEG C, leave standstill supersound process 10-15 minute after 15-20 hour, wash, filter, dry to constant weight and get final product.
The technical parameter index of the xylon using the present invention to produce is as follows:
(1) pliability fluffy smooth flexible, intensity is high;
(2) oxygen index (OI): 27.8%, flame retardant effect is excellent;
(3) bacteriostasis rate of finished product to intestinal bacteria, streptococcus aureus, Candida albicans is all greater than 99.8%.
Claims (2)
1. the xylon that an energy is radiation infrared, it is characterized in that, be made up of the raw material of following weight part: xylon 40-44, medium staple cotton fiber 7-9, viscose fiber 5-8, mountain palm fibre fiber 6-10, Sugarcane peel. 20-25, tea rim charge 17-19, infrared ceramic powder 1-3, polystyrene nanoparticles 1.2-2.5, carnauba wax 4-7, ethanol 10-13, polyvinylacetal 4-8, Bis(lauroyloxy)dioctyltin 0.3-0.7, agate card 3-4, Yanhusuo 2-4, red sage root 1-2, auxiliary agent 3-6, suitable quantity of water, described auxiliary agent is made up of following raw materials in part by weight: tealeaves fiber 10-13, nano zine oxide 2-4, silicon powder 1-3, dual polyethylene polydimethylsiloxane 0.03-0.05, glyceryl monostearate 1.2-3.1, polyoxyethylene glycol 3-6, methylisothiazolinone 2.1-3.6, Oleum Pelargonii Graveolentis 3.2-4.7, Flos Pelargonii Hortori 0.2-0.4, linolic acid 1.3-2.4, Dyhard RU 100 0.1-0.2, ethyl acrylate 4-7, fire retardant CP 0.04-0.07, its preparation method be first by nano zine oxide ultrasonic disperse in polyoxyethylene glycol, add tealeaves blending in of fibers and stir 5-8 hour, take out drying and grinding 10-15 minute, obtained modification tealeaves fiber, then by Oleum Pelargonii Graveolentis, Flos Pelargonii Hortori adds water stirring, and add silicon powder and stir 30-40 minute, spraying dry obtains modified silicon micro mist, finally by ethyl acrylate, linolic acid, Dyhard RU 100, methylisothiazolinone stirring and evenly mixing, adds above-mentioned obtained modification tealeaves fiber and modified silicon micro mist, glyceryl monostearate, dual polyethylene polydimethylsiloxane, fire retardant CP supersound process 30-40 minute and get final product.
2. the making method of the xylon that a kind of energy according to claim 1 is radiation infrared, is characterized in that comprising the following steps:
(1) add water after getting Sugarcane peel., tea rim charge, agate card, Yanhusuo, the red sage root pulverizing boiling pulping, adds infrared ceramic powder agitation grinding 20-30 minute, send in defibrator and be processed into modified composite fiber;
(2) by ethanol, polyvinylacetal heated and stirred, carnauba wax, polystyrene nanoparticles, Bis(lauroyloxy)dioctyltin supersound process 20-40 minute is added;
(3) xylon, medium staple cotton fiber, viscose fiber, mountain palm fibre fiber, modified composite fiber are put into pulverizing mill and worn into 80-100 order powder, putting into high mixer after drying mixes to 80-90 DEG C, add step (2) reaction product and remaining component is mixed to 100-120 DEG C, leave standstill supersound process 10-15 minute after 15-20 hour, wash, filter, dry to constant weight and get final product.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201410454661.1A CN104277469A (en) | 2014-09-09 | 2014-09-09 | Wood fiber capable of radiating far-infrared rays and manufacturing method thereof |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201410454661.1A CN104277469A (en) | 2014-09-09 | 2014-09-09 | Wood fiber capable of radiating far-infrared rays and manufacturing method thereof |
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| Publication Number | Publication Date |
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| CN104277469A true CN104277469A (en) | 2015-01-14 |
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| Application Number | Title | Priority Date | Filing Date |
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| CN201410454661.1A Pending CN104277469A (en) | 2014-09-09 | 2014-09-09 | Wood fiber capable of radiating far-infrared rays and manufacturing method thereof |
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| Country | Link |
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| CN (1) | CN104277469A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2018095150A1 (en) * | 2016-11-23 | 2018-05-31 | 浙江农林大学 | Method for preparing nanometer material/biomass fiber composite, and nanometer material/biomass fiber composite |
| WO2022056432A1 (en) | 2020-09-14 | 2022-03-17 | Arxada Ag | Biocidal composition and method |
| WO2022198049A1 (en) | 2021-03-19 | 2022-09-22 | Arxada, LLC | Biocidal composition and method |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0302141A2 (en) * | 1987-08-07 | 1989-02-08 | Descente Ltd. | Solar heat selective absorptive fiber material |
| JPH0369675A (en) * | 1989-08-07 | 1991-03-26 | Teijin Ltd | Wear-resistant far infrared ray-radiating synthetic fiber |
| CN1140770A (en) * | 1995-07-14 | 1997-01-22 | 第一合纤株式会社 | Method for manufacturing far infrared-radiating polyester fibers |
| CN103966695A (en) * | 2014-04-23 | 2014-08-06 | 安徽依采妮纤维材料科技有限公司 | Healthcare ramie fiber fabric and preparation method thereof |
-
2014
- 2014-09-09 CN CN201410454661.1A patent/CN104277469A/en active Pending
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0302141A2 (en) * | 1987-08-07 | 1989-02-08 | Descente Ltd. | Solar heat selective absorptive fiber material |
| JPH0369675A (en) * | 1989-08-07 | 1991-03-26 | Teijin Ltd | Wear-resistant far infrared ray-radiating synthetic fiber |
| CN1140770A (en) * | 1995-07-14 | 1997-01-22 | 第一合纤株式会社 | Method for manufacturing far infrared-radiating polyester fibers |
| CN103966695A (en) * | 2014-04-23 | 2014-08-06 | 安徽依采妮纤维材料科技有限公司 | Healthcare ramie fiber fabric and preparation method thereof |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2018095150A1 (en) * | 2016-11-23 | 2018-05-31 | 浙江农林大学 | Method for preparing nanometer material/biomass fiber composite, and nanometer material/biomass fiber composite |
| WO2022056432A1 (en) | 2020-09-14 | 2022-03-17 | Arxada Ag | Biocidal composition and method |
| CN116347983A (en) * | 2020-09-14 | 2023-06-27 | 阿萨达股份公司 | Biocidal compositions and methods |
| EP4199719A4 (en) * | 2020-09-14 | 2024-09-04 | Arxada AG | BIOCIDAL COMPOSITION AND METHOD |
| WO2022198049A1 (en) | 2021-03-19 | 2022-09-22 | Arxada, LLC | Biocidal composition and method |
| EP4291030A4 (en) * | 2021-03-19 | 2024-09-11 | Arxada, LLC | BIOCIDAL COMPOSITION AND METHOD |
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Application publication date: 20150114 |
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