Movatterモバイル変換


[0]ホーム

URL:


CN104594025A - Method for preparing novel zinc-oxide-modified ultraviolet-resistant silk - Google Patents

Method for preparing novel zinc-oxide-modified ultraviolet-resistant silk
Download PDF

Info

Publication number
CN104594025A
CN104594025ACN201510055927.XACN201510055927ACN104594025ACN 104594025 ACN104594025 ACN 104594025ACN 201510055927 ACN201510055927 ACN 201510055927ACN 104594025 ACN104594025 ACN 104594025A
Authority
CN
China
Prior art keywords
silk
zinc
preparation
uvioresistant
novel oxidized
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.)
Granted
Application number
CN201510055927.XA
Other languages
Chinese (zh)
Other versions
CN104594025B (en
Inventor
陈永林
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.)
Shenzhen warm home textile Co., Ltd.
Original Assignee
HUZHOU XINCHUANG SILK 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 HUZHOU XINCHUANG SILK CO LtdfiledCriticalHUZHOU XINCHUANG SILK CO Ltd
Priority to CN201510055927.XApriorityCriticalpatent/CN104594025B/en
Publication of CN104594025ApublicationCriticalpatent/CN104594025A/en
Application grantedgrantedCritical
Publication of CN104594025BpublicationCriticalpatent/CN104594025B/en
Expired - Fee Relatedlegal-statusCriticalCurrent
Anticipated expirationlegal-statusCritical

Links

Landscapes

Abstract

The invention discloses a method for preparing novel zinc-oxide-modified ultraviolet-resistant silk. According to the method, a zinc oxide film layer covers the surface of the silk by adopting an in situ synthesis method. The method specifically comprises the following steps: degumming the silk and performing surface activation; respectively dipping the silk in a zinc precursor solution and a reaction solvent; and finally, adding the silk into a heated and humidified steam, standing, taking out the silk, washing, and drying, thereby obtaining the zinc-oxide-modified ultraviolet-resistant silk. The preparation method is simple, convenient, high in efficiency and low in cost, solves the problem that zinc oxide is difficult to disperse and is suitable for large-scale production. The zinc oxide film layer covers the surface of the silk modified by the method, and the silk has high ultraviolet resistance, and improved mechanical property.

Description

A kind of preparation method of uvioresistant silk of novel oxidized zinc modification
Technical field:
The invention belongs to silk product technical field, particularly a kind of preparation method of uvioresistant silk of novel oxidized zinc modification.
Background technology:
Silk is thread azelon, containing 18 seed amino acids, these amino acid can produce photochemical reaction with ultraviolet, but very strong photochemical reaction can make the peptide bond of silk protein molecular backbone rupture, cause the mechanical strength of silk to decline and yellowing, affect the usability of silk, although therefore silk itself has certain protective action to ultraviolet, but the protective action of itself is very faint, need to carry out anti-ultraviolet finishing.
The uvioresistant material of conventional textiles mainly divides organic uv absorbers and inorganic UV screener, and organic uv absorbers becomes the mode of light and heat to discharge ultraviolet power conversion, and inorganic UV screener is by ultraviolet reflection or scattering.Organic uv absorbers is mainly salicylate system, benzophenone series, benzotriazole system and triazine system etc., the photostability of such material is poor, service life is short, can make fabric variable color, irritant etc. to skin, inorganic UV screener is mainly the particulate such as zinc oxide, titanium dioxide, good to the full wave shielding of UVB, and good light stability, arrange in colourless, on fabric color without impact, and environmentally friendly etc.
The anti-ultraviolet finishing of silk generally adopts organic uv absorbers, but along with expanding economy, to the raising that environment and quality of the life require, inorganic UV screener more and more receives publicity, and is wherein that the developing direction of the high-performance ultraviolet light screener supported is particularly wide with nanometer technology.
Chinese patent CN 101187164B (publication date 2008.07.23) discloses a kind of anti-creasing anti-bacterial anti-violet composite function silk fabric, is to be padded in by silk fabric in multifunction finishing agent that nano titanic oxide sol and Fibroin Hydrolysis liquid is mixed with to obtain.The disclosed functionalized nano shitosan of Chinese patent CN102677465B (publication date 2012.11.14) and nano-titanium dioxide modified tussah silk textiles, tussah silk woven fabric or nonwoven fabric are immersed in shitosan and titania solution, obtains the tussah silk textiles of modification.Chinese patent CN 103572585A (publication date 2014.02.12) discloses a kind of titania modified silk, is take titanate esters as reactant and benzinum for solvent generates fine and close titanium dioxide at silk surface in situ.Current nano titanium oxide is comparatively extensive as the application of anti ultraviolet agent on silk fabric, but the application of nano zine oxide is less.
Summary of the invention:
The object of this invention is to provide a kind of preparation method of uvioresistant silk of novel oxidized zinc modification, after the surface active by silk, impregnated in precursor solution and the reaction solution of zinc respectively, form zinc hydroxide film through reaction in-situ on silk surface, obtain the silk of modified zinc oxide finally by high temperature steam treatment.This preparation method is easy, and cost is low, is applicable to being applied in large-scale production, and the silk of preparation possesses higher ultraviolet-resistent property and mechanical performance.
Object of the present invention is achieved through the following technical solutions:
A preparation method for the uvioresistant silk of novel oxidized zinc modification, it is characterized in that, the method comprises the following steps:
(1) after silk being removed impurity, to come unstuck 60min with the sodium bicarbonate solution of 0.05g/L, spend deionized water clean, 40 DEG C of dryings obtain the silk come unstuck;
(2) after the surface activation process of the silk come unstuck step (1) obtained, 35-50s in the precursor solution of zinc is impregnated in bath raio 1:40, be soaked in reaction dissolvent with bath raio 1:30 again, at 60-70 DEG C, react 5-10min, take out the silk obtaining zinc hydroxide and cover;
(3) steam that the silk that zinc hydroxide step (2) obtained covers is placed in warming and humidifying leaves standstill, and takes out washing and dries, obtain the silk of modified zinc oxide.
Preferred as technique scheme, the silk described in step (1) is mulberry silk, tussah silk or regenerated fibroin fiber.
Preferred as technique scheme, the surface activation process described in step (1) is Cement Composite Treated by Plasma or soaks strong oxidizer.
Preferred as technique scheme, described oxidant is liquor potassic permanganate.
Preferred as technique scheme, the zinc nitrate hexahydrate aqueous solution of the precursor solution of the zinc described in step (2) to be mass fraction be 20-30%.
Preferred as technique scheme, the ammoniacal liquor of to be mass fraction the be 40-50% of the reaction dissolvent described in step (2).
Preferred as technique scheme, the steam of the warming and humidifying described in step (3) is the mixed vapour of ammoniacal liquor and water, and the volume ratio of ammoniacal liquor and water is 2:1, and the temperature of steam is 125-130 DEG C, and humidity is 20%.
Preferred as technique scheme, the time left standstill described in step (3) is 15-20min.
Preferred as technique scheme, the number of times of the washing described in step (3) is 2-3 time.
Preferred as technique scheme, the temperature of the oven dry described in step (3) is 30 DEG C.
Compared with prior art, the present invention has the following advantages:
(1) the present invention adopts silk surface active in conjunction with the Surface Creation one deck zinc-oxide film of in-situ synthesis at silk, and avoid the problem of zinc oxide difficulty dispersion, preparation method is easy, and cost is low, is applicable to large-scale production.
(2) preparation method that the present invention adopts adopts simple dipping gimmick, but adopt of short duration dipping repeatedly in conjunction with the means of moist steam, in the atmosphere of wet-hot steam, the synthesis of accelerating oxidation zinc, the generation nano granular of zinc oxide that the method energy is slowly gentle, to the surface almost not damaged of silk.
(3) silk of this method modification uniformly covers the thick zinc-oxide film of one deck 200nm, except giving silk good uvioresistant performance, going back bacteriostasis antibiosis deodorizing, and improving the mechanical performance of silk.
Detailed description of the invention:
In order to deepen the understanding of the present invention, below in conjunction with embodiment, the invention will be further described, and this embodiment only for explaining the present invention, does not form limiting the scope of the present invention.
Embodiment 1:
(1) after mulberry silk being removed impurity, to come unstuck 60min with the sodium bicarbonate solution of 0.05g/L, spend deionized water clean, 40 DEG C of dryings obtain the silk come unstuck.
(2) by the silk that comes unstuck after plasma treated surface activation, 50s in the zinc nitrate hexahydrate aqueous solution of 20% is impregnated in bath raio 1:40, be soaked in the ammoniacal liquor of 40% with bath raio 1:30 again, at 60 DEG C, react 10min, take out the silk obtaining zinc hydroxide and cover.
(3) be placed in by the silk that zinc hydroxide covers, volume ratio is in ammoniacal liquor and the water mixed vapour of 2:1, is 20% time in humidity, 125 DEG C of standing 20min, and taking-up washing 2 times, 30 DEG C of oven dry obtain the silk of modified zinc oxide.
Embodiment 2:
(1) after tussah silk being removed impurity, to come unstuck 60min with the sodium bicarbonate solution of 0.05g/L, spend deionized water clean, 40 DEG C of dryings obtain the silk come unstuck.
(2) after the Silk Soaking liquor potassic permanganate treatment surface of coming unstuck being activated, 50s in the zinc nitrate hexahydrate aqueous solution of 20% is impregnated in bath raio 1:40, be soaked in the ammoniacal liquor of 40% with bath raio 1:30 again, at 70 DEG C, react 5min, take out the silk obtaining zinc hydroxide and cover.
(3) silk that zinc hydroxide covers being placed in the ammoniacal liquor and water mixed vapour that volume ratio is 2:1, is 20% time in humidity, 130 DEG C of standing 15min, and take out washing 3 times, 30 DEG C of oven dry obtain the silk of modified zinc oxide.
Embodiment 3:
(1) after regenerated fibroin fiber being removed impurity, to come unstuck 60min with the sodium bicarbonate solution of 0.05g/L, spend deionized water clean, 40 DEG C of dryings obtain the silk come unstuck.
(2) by the silk that comes unstuck after plasma treated surface activation, 40s in the zinc nitrate hexahydrate aqueous solution of 25% is impregnated in bath raio 1:40, be soaked in the ammoniacal liquor of 45% with bath raio 1:30 again, at 65 DEG C, react 7min, take out the silk obtaining zinc hydroxide and cover.
(3) be placed in by the silk that zinc hydroxide covers, volume ratio is in ammoniacal liquor and the water mixed vapour of 2:1, is 20% time in humidity, 127 DEG C of standing 17min, and taking-up washing 3 times, 30 DEG C of oven dry obtain the silk of modified zinc oxide.
Embodiment 4:
(1) after mulberry silk being removed impurity, to come unstuck 60min with the sodium bicarbonate solution of 0.05g/L, spend deionized water clean, 40 DEG C of dryings obtain the silk come unstuck.
(2) after the Silk Soaking liquor potassic permanganate treatment surface of coming unstuck being activated, 48s in the zinc nitrate hexahydrate aqueous solution of 29% is impregnated in bath raio 1:40, be soaked in the ammoniacal liquor of 42% with bath raio 1:30 again, at 67 DEG C, react 10min, take out the silk obtaining zinc hydroxide and cover.
(3) be placed in by the silk that zinc hydroxide covers, volume ratio is in ammoniacal liquor and the water mixed vapour of 2:1, is 20% time in humidity, 126 DEG C of standing 16min, and taking-up washing 3 times, 30 DEG C of oven dry obtain the silk of modified zinc oxide.
Embodiment 5:
(1) after regenerated fibroin fiber being removed impurity, to come unstuck 60min with the sodium bicarbonate solution of 0.05g/L, spend deionized water clean, 40 DEG C of dryings obtain the silk come unstuck.
(2) by the silk that comes unstuck after plasma treated surface activation, 50s in the zinc nitrate hexahydrate aqueous solution of 30% is impregnated in bath raio 1:40, be soaked in the ammoniacal liquor of 50% with bath raio 1:30 again, at 70 DEG C, react 10min, take out the silk obtaining zinc hydroxide and cover.
(3) be placed in by the silk that zinc hydroxide covers, volume ratio is in ammoniacal liquor and the water mixed vapour of 2:1, is 20% time in humidity, 130 DEG C of standing 20min, and taking-up washing 3 times, 30 DEG C of oven dry obtain the silk of modified zinc oxide.
Embodiment 6:
(1) after tussah silk being removed impurity, to come unstuck 60min with the sodium bicarbonate solution of 0.05g/L, spend deionized water clean, 40 DEG C of dryings obtain the silk come unstuck.
(2) after the Silk Soaking liquor potassic permanganate treatment surface of coming unstuck being activated, 35s in the zinc nitrate hexahydrate aqueous solution of 20% is impregnated in bath raio 1:40, be soaked in the ammoniacal liquor of 40-50% with bath raio 1:30 again, at 60 DEG C, react 5min, take out the silk obtaining zinc hydroxide and cover.
(3) be placed in by the silk that zinc hydroxide covers, volume ratio is in ammoniacal liquor and the water mixed vapour of 2:1, is 20% time in humidity, 125 DEG C of standing 15min, and taking-up washing 3 times, 30 DEG C of oven dry obtain the silk of modified zinc oxide.
The uvioresistant silk fabric of the modified zinc oxide prepared by embodiment 1-6 is compared with untreated silk fabric, and the grammes per square metre of silk fabric, ultraviolet-resistent property, antibiotic property and mechanical properties results are as shown in the table:
From above-mentioned data, the anti-ultraviolet property of the uvioresistant silk fabric of modified zinc oxide prepared by this method is excellent, and the antibiotic property of fabric and mechanical strength have lifting.

Claims (10)

CN201510055927.XA2015-02-032015-02-03Method for preparing zinc-oxide-modified ultraviolet-resistant silkExpired - Fee RelatedCN104594025B (en)

Priority Applications (1)

Application NumberPriority DateFiling DateTitle
CN201510055927.XACN104594025B (en)2015-02-032015-02-03Method for preparing zinc-oxide-modified ultraviolet-resistant silk

Applications Claiming Priority (1)

Application NumberPriority DateFiling DateTitle
CN201510055927.XACN104594025B (en)2015-02-032015-02-03Method for preparing zinc-oxide-modified ultraviolet-resistant silk

Publications (2)

Publication NumberPublication Date
CN104594025Atrue CN104594025A (en)2015-05-06
CN104594025B CN104594025B (en)2017-02-15

Family

ID=53120059

Family Applications (1)

Application NumberTitlePriority DateFiling Date
CN201510055927.XAExpired - Fee RelatedCN104594025B (en)2015-02-032015-02-03Method for preparing zinc-oxide-modified ultraviolet-resistant silk

Country Status (1)

CountryLink
CN (1)CN104594025B (en)

Cited By (14)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
CN105686159A (en)*2016-03-142016-06-22浙江大学Method for preparing novel mask chip by utilizing fibroin plate cocoons
CN105803805A (en)*2016-04-212016-07-27安徽皖翎羽绒制品有限公司Treatment method of anti-bacterial and anti-UV (Ultraviolet) down feather
CN106149352A (en)*2016-08-092016-11-23东华大学A kind of preparation method of nano zinc oxide modified bafta
CN106835673A (en)*2017-03-272017-06-13广西科技大学A kind of UV resistance zinc oxide silk composite fiber and preparation method thereof
CN107287877A (en)*2017-06-282017-10-24合肥市聚丰制丝有限责任公司It is a kind of to improve the method for silk performance
CN107313244A (en)*2017-07-162017-11-03长沙善道新材料科技有限公司The technique that a kind of use silk prepares uvioresistant antibiotic fabric
CN107419519A (en)*2017-07-162017-12-01长沙善道新材料科技有限公司A kind of preparation method of the affine uvioresistant anti bacteria natural silk fiber of zinc oxide
CN107630351A (en)*2017-09-292018-01-26安徽省创安体育用品有限公司A kind of preparation method of Anti-static cap cloth
CN109680480A (en)*2018-11-282019-04-26湖州品创孵化器有限公司A kind of preparation method of health uvioresistant silk fabric
CN109695150A (en)*2018-11-282019-04-30湖州品创孵化器有限公司A kind of preparation method of pro-skin type uvioresistant silk fabric
CN111136968A (en)*2019-08-272020-05-12深圳市大毛牛新材料科技有限公司Waterproof anti ultraviolet textile fabric
CN113832729A (en)*2021-09-152021-12-24苏州同构科技有限公司Washable ultraviolet absorbent and preparation method thereof
CN114673006A (en)*2022-03-082022-06-28浙江理工大学 An antibacterial medical textile coating material based on ZnO-silk fibroin
CN115961466A (en)*2022-11-282023-04-14北京工业大学 A preparation method for in-situ growth of nano ZnO antibacterial film on natural fabric

Citations (4)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
CN101012621A (en)*2007-01-302007-08-08东华大学Preparation method of zinc oxide nano-rod film on fibre product
US8277518B1 (en)*2011-10-112012-10-02The Sweet Living Group, LLCEcological fabric having ultraviolet radiation protection
CN103194885A (en)*2013-04-192013-07-10中国民航大学Method for microwave synthesis of nano-ZnO assembled cotton fibers
CN103898735A (en)*2014-04-112014-07-02西南大学Preparation method and product of zinc oxide nanorod matrix modified silk

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
CN101012621A (en)*2007-01-302007-08-08东华大学Preparation method of zinc oxide nano-rod film on fibre product
US8277518B1 (en)*2011-10-112012-10-02The Sweet Living Group, LLCEcological fabric having ultraviolet radiation protection
CN103194885A (en)*2013-04-192013-07-10中国民航大学Method for microwave synthesis of nano-ZnO assembled cotton fibers
CN103898735A (en)*2014-04-112014-07-02西南大学Preparation method and product of zinc oxide nanorod matrix modified silk

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
王晓婧等: "纳米材料原位固着技术开发多功能真丝面料", 《印染助剂》*

Cited By (17)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
CN105686159B (en)*2016-03-142018-02-02浙江大学A kind of method that gauze mask chip is prepared using fibroin plate cocoon
CN105686159A (en)*2016-03-142016-06-22浙江大学Method for preparing novel mask chip by utilizing fibroin plate cocoons
CN105803805A (en)*2016-04-212016-07-27安徽皖翎羽绒制品有限公司Treatment method of anti-bacterial and anti-UV (Ultraviolet) down feather
CN106149352A (en)*2016-08-092016-11-23东华大学A kind of preparation method of nano zinc oxide modified bafta
CN106835673A (en)*2017-03-272017-06-13广西科技大学A kind of UV resistance zinc oxide silk composite fiber and preparation method thereof
CN107287877A (en)*2017-06-282017-10-24合肥市聚丰制丝有限责任公司It is a kind of to improve the method for silk performance
CN107419519A (en)*2017-07-162017-12-01长沙善道新材料科技有限公司A kind of preparation method of the affine uvioresistant anti bacteria natural silk fiber of zinc oxide
CN107313244A (en)*2017-07-162017-11-03长沙善道新材料科技有限公司The technique that a kind of use silk prepares uvioresistant antibiotic fabric
CN107630351A (en)*2017-09-292018-01-26安徽省创安体育用品有限公司A kind of preparation method of Anti-static cap cloth
CN109680480A (en)*2018-11-282019-04-26湖州品创孵化器有限公司A kind of preparation method of health uvioresistant silk fabric
CN109695150A (en)*2018-11-282019-04-30湖州品创孵化器有限公司A kind of preparation method of pro-skin type uvioresistant silk fabric
CN111136968A (en)*2019-08-272020-05-12深圳市大毛牛新材料科技有限公司Waterproof anti ultraviolet textile fabric
CN111136968B (en)*2019-08-272022-05-27江苏大毛牛新材料有限公司Waterproof anti ultraviolet textile fabric
CN113832729A (en)*2021-09-152021-12-24苏州同构科技有限公司Washable ultraviolet absorbent and preparation method thereof
CN114673006A (en)*2022-03-082022-06-28浙江理工大学 An antibacterial medical textile coating material based on ZnO-silk fibroin
CN114673006B (en)*2022-03-082023-09-29浙江理工大学Antibacterial medical textile coating material based on ZnO-silk fibroin
CN115961466A (en)*2022-11-282023-04-14北京工业大学 A preparation method for in-situ growth of nano ZnO antibacterial film on natural fabric

Also Published As

Publication numberPublication date
CN104594025B (en)2017-02-15

Similar Documents

PublicationPublication DateTitle
CN104594025A (en)Method for preparing novel zinc-oxide-modified ultraviolet-resistant silk
CN103397513B (en)The nano titanic oxide sol finishing agent of low-temperature growth and application thereof
CN103643481B (en)A kind of preparation method of carbon fiber surface aluminum oxide coating layer
CN109603919B (en) A kind of high-efficiency photocatalytic degradation material that can be recycled and preparation method thereof
CN110093775A (en)A kind of preparation method of the uvioresistant cotton fabric of conductive energy
CN103877971A (en)Efficient visible-light-induced photocatalyst and preparation method thereof
CN102698730B (en)Preparation method of hollow boron/cerium co-doped nanometer titanium dioxide fiber material
CN108442099B (en)Anti-ultraviolet nano zinc oxide composite textile fabric and preparation method thereof
CN107513174A (en)A kind of preparation method of cellulose/nanometer cerium oxide composite membrane
CN105862396B (en)A kind of surface modification of aramid fiber and preparation method thereof
CN106622210A (en)Method for synthesizing urchin-shaped tungsten oxide
CN108212187B (en) Preparation method of Fe-doped Bi2O2CO3 photocatalyst and Fe-doped Bi2O2CO3 photocatalyst
CN107352519B (en)A kind of C3N4The preparation method of nano wire
CN105401404A (en)Fabric for treating printing and dyeing wastewater and preparation method of fabric
CN106140241A (en) Nano g-C3N4 organic photocatalyst regulated by oxygen ion surface and its preparation method and application
CN104233786A (en)Method for producing silk fabric functionalized by titanium dioxide nanoparticles
CN102251389B (en)Method for modifying polyester fabric by using butyl titanate
CN101703925B (en)Thulium doped titanium sol and method for degrading textile organic dirt under visible light
CN103288128A (en)A method for the synthesis of flaky anatase type titanium dioxide by using biological templates
CN106902760B (en)A kind of eggshell load zinc oxide material and its preparation method and application
CN110747628B (en)Preparation method of superfine fiber artificial leather with photocatalysis function
CN108325547A (en)Composite photo-catalyst shell base boron-doped titanium dioxide and preparation method thereof
CN104492435B (en) A CuO/TiO2/graphene composite photocatalyst with (001) active surface as the main component and its preparation method
CN108755103B (en)Preparation method of photocatalytic self-cleaning anti-ultraviolet fabric
CN117920276A (en) A 1T-WS2/TiO2 composite fiber membrane catalyst and preparation method thereof

Legal Events

DateCodeTitleDescription
C06Publication
PB01Publication
C10Entry into substantive examination
SE01Entry into force of request for substantive examination
C41Transfer of patent application or patent right or utility model
CB03Change of inventor or designer information

Inventor after:Wang Junhong

Inventor before:Chen Yonglin

CORChange of bibliographic data
TA01Transfer of patent application right

Effective date of registration:20161114

Address after:518000, Guangdong, Longhua province Shenzhen New District Guanlan street, Tong Hang Kong community, A8 Industrial Zone, the first floor of the southern tip of the first floor, two, three

Applicant after:Shenzhen warm home textile Co., Ltd.

Address before:313026 Zhejiang Province, Huzhou city Nanxun District Hefu town re trillion Industrial Park

Applicant before:Huzhou Xinchuang Silk Co., Ltd.

C14Grant of patent or utility model
GR01Patent grant
CF01Termination of patent right due to non-payment of annual fee

Granted publication date:20170215

Termination date:20180203

CF01Termination of patent right due to non-payment of annual fee

[8]ページ先頭

©2009-2025 Movatter.jp