CN102154829A - Fuzzing, pilling and ultraviolet-prevention finishing agent and preparation method and application - Google Patents

Fuzzing, pilling and ultraviolet-prevention finishing agent and preparation method and application Download PDF

Info

Publication number
CN102154829A
CN102154829A CN 201010595876 CN201010595876A CN102154829A CN 102154829 A CN102154829 A CN 102154829A CN 201010595876 CN201010595876 CN 201010595876 CN 201010595876 A CN201010595876 A CN 201010595876A CN 102154829 A CN102154829 A CN 102154829A
Authority
CN
China
Prior art keywords
finishing agent
acid
titanium alkoxide
alkoxide
mixture
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
CN 201010595876
Other languages
Chinese (zh)
Other versions
CN102154829B (en
Inventor
王然
陈英
王锐
陈静茹
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.)
Lancy Co ltd
Original Assignee
Beijing Institute Fashion Technology
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 Institute Fashion Technology filed Critical Beijing Institute Fashion Technology
Priority to CN 201010595876 priority Critical patent/CN102154829B/en
Publication of CN102154829A publication Critical patent/CN102154829A/en
Application granted granted Critical
Publication of CN102154829B publication Critical patent/CN102154829B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

The invention discloses a fuzzing, pilling and ultraviolet-prevention finishing agent and preparation method and application. The finishing agent is prepared by the method comprising the following steps: (1) dissolving titanium alkoxide in an organic solvent, adding the obtained solution into acid aqueous solution and stirring uniformly to obtain a mixture; and (2) adding silicon alkoxide into the mixture obtained in the step (1), and stirring uniformly to obtain transparent solution; or (1) sequentially dissolving acid and silicon alkoxide in water, and stirring uniformly to obtain a mixture; and (2) dissolving titanium alkoxide in an organic solvent, adding the obtained solution into the mixture obtained in the step (1), and stirring uniformly to obtain transparent solution. The finishing agent disclosed by the invention is simple in preparation and short in the finishing process, and meets the requirements of water and energy conservation, low carbon and environmental protection.

Description

The anti-ultraviolet finishing agent of a kind of anti-pilling and preparation method and application
Technical field
The invention belongs to the finishing functions of textile fabrics field, relate to a kind of finishing agent, particularly a kind of anti-pilling, anti-ultraviolet finishing agent, and preparation method thereof with application.
Background technology
Finishing functions is the important means that promotes the textiles wearability, increases the textiles added value, mainly comprise anti-ultraviolet, anti-pilling, wrinkle resistant, antibiotic, refuse water, refuse oil, felt proofing, fire-retardant, softness etc.Because the mechanism of every kind of finishing functions has nothing in common with each other, therefore often need to adopt different finishing auxiliarieses.Along with developing rapidly of consumption demand, requirement improves constantly to functions of textile fabrics, and especially textiles being had polyfunctional requirement simultaneously increases gradually.
Anti-pilling and the arrangement of anti-ultraviolet are textile two kinds of arrangements often adopting with polyester cotton.Anti-ultraviolet arrangement is main by ultraviolet absorption and reflection are realized, mainly adopts Oxybenzone, hydroxy-phenyl benzotriazole, hydroxyphenyl-triazine etc.; In addition, nano titanium oxide also has certain ultraviolet shielded effect.Pill resistant finish is an approach to reduce interfibrous slippage or to increase surface of cotton fabric fineness, and biology enzyme, polyacrylate, polyurethane, organo-silicon compound etc. are main auxiliary agent.
When Oxybenzone, hydroxy-phenyl benzotriazole, hydroxyphenyl-triazine and biology enzyme carried out with the bath processing to textiles, biological enzyme activity can be affected, and weakens finishing effect; And during auxiliary agent couplings such as the anti-ultraviolet finishing agent of tradition and polyacrylate, polyurethane, organo-silicon compound, colloidal sol, will reduce the diffusivity of preventing the ultraviolet finishing agent again.Therefore at present textiles realizes that if desired anti-pilling is functional with two kinds of anti-ultraviolets, must carry out a kind of arrangement earlier and realize once putting in order after a kind of function again and realize another kind of function, processing technology complexity, water consumption power consumption, increase cost.
Therefore study the anti-pilling of textiles, anti-ultraviolet mechanism, the development of new finishing agent is realized single bath process, reduces the pollution of chemical assistant to environment, cuts down the consumption of energy, and this is one of main developing direction in current finishing functions field.
Summary of the invention
At the deficiency of existing processing technology, the invention provides a kind of anti-pilling that can make by single bath process, the finishing functions of textile fabrics agent of anti-ultraviolet.
One of purpose of the present invention is to provide the anti-pilling of this kind, anti-ultraviolet finishing agent.Described finishing agent is got by the method preparation that may further comprise the steps:
(1) the titanium alkoxide is dissolved in the organic solvent, the solution with gained adds in the acidic aqueous solution again, stirs, and obtains mixture;
(2) silicon alkoxide is joined in the mixture that obtains in the step (1), stir, obtain clear solution, promptly described finishing agent;
Perhaps get by the method preparation that may further comprise the steps:
(1) acid, silicon alkoxide is soluble in water successively, stir, obtain mixture;
(2) the titanium alkoxide is dissolved in the organic solvent, the solution of gained joins in the mixture that obtains in the step (1), stirs, and obtains clear solution, promptly described finishing agent;
In two kinds of above-mentioned preparation processes, preferred first kind.
More specifically,
Described silicon alkoxide is selected from least a in C4~C20 alkoxy silane; Preferred at least a in C4~C9 alkoxy silane.More specifically examples of compounds comprises: methyl silicate, ethyl orthosilicate, γ-glycidyl ether oxygen propyl trimethyl oxosilane, vinyl trimethyl oxosilane, vinyl triethyl group oxosilane, γ-(methacryloxy) oxypropyl trimethyl oxosilane; Wherein, preferred γ-glycidyl ether oxygen propyl trimethyl oxosilane, vinyl trimethyl oxosilane.
Described titanium alkoxide is selected from least a in C8~C20 alkoxytitanium acid esters; Preferred at least a in C8~C16 alkoxytitanium acid esters.More specifically examples of compounds comprises: butyl titanate, metatitanic acid four n-propyls, tetraisopropyl titanate, metatitanic acid four isobutyl esters, tetraethyl titanate; Wherein, preferred butyl titanate.
Described acid is selected from least a in inorganic acid or the water miscible organic acid; Preferred at least a in hydrochloric acid, nitric acid, formic acid.
Described organic solvent is to form chelate structure and water-soluble organic solvent with the titanium alkoxide, is selected from least a in the hydroxyl organic ligand compound; Preferred at least a in acetic acid, acetylacetone,2,4-pentanedione.Wherein, the consumption of each component is as follows:
The mol ratio of described titanium alkoxide and water is 1: (1~200); Preferred 1: (30~100);
The mol ratio of described titanium alkoxide and organic solvent is 1: (0.5~100); Preferred 1: (4~10);
Described titanium alkoxide is 1 with the mol ratio of acid: (0.001~10); Preferred 1: (0.01~0.1);
The mol ratio of described titanium alkoxide and silicon alkoxide is 1: (0.01~100); Preferred 1: (1~10).
The effect of finishing agent of the present invention is the mating reaction of each reagent, and its consumption can be regulated in the scope of broad, and effect is not had much affect.
It is raw material that the present invention adopts titanium alkoxide and silicon alkoxide, utilize them that hydrolysis and polycondensation reaction take place in water, generation is uniformly distributed in the water, the nano particle that contains Si-O-Si, Ti-O-Ti, Si-O-Ti key, because the Ti-O key has excellent uvioresistant performance, and Si-O has two dimension and three-dimensional valence bond structure simultaneously, the two in conjunction with after also can improve the anti-pilling of fabric.In addition, because nanostructured has than bigger serface, can be spontaneous absorption fast takes place, assemble at fabric face so do not need to add any adhesive in the finishing agent, and safer environmental protection has also reduced cost simultaneously.
Two of purpose of the present invention is to provide the preparation method of this kind finishing agent, and this preparation method is the single bath process process, may further comprise the steps:
(1) the titanium alkoxide is dissolved in the organic solvent, the solution with gained adds in the acidic aqueous solution again, stirs, and obtains mixture;
(2) silicon alkoxide is joined in the mixture that step (1) obtains, stir, obtain clear solution, promptly described finishing agent;
Perhaps described method may further comprise the steps:
(1) acid, silicon alkoxide is soluble in water successively, stir, obtain mixture;
(2) the titanium alkoxide is dissolved in the organic solvent, the solution of gained joins in the mixture that obtains in the step (1), stirs, and obtains clear solution, promptly described finishing agent.
In the described operation, the interpolation of its material and alr mode are common processing method.
Three of purpose of the present invention is to provide the purposes of this kind finishing agent, and described finishing agent is used to put in order pure cotton fabric, or chemical fibre and cotton blended fabric.
Wherein, described chemical fibre is selected from least a in polyester fiber, polyamide fiber, the polypropylene fibre.Textiles in the described step (2) is cotton or chemical fibre and cotton blended fabric, and wherein chemical fibre comprises polyester fiber, polyamide fiber, polypropylene fibre etc.
When using finishing agent of the present invention to put textiles in order, can finishing agent of the present invention be handled on the textiles by padding or flood single bath process, liquid carrying rate is 40~100%, and oven dry baked in 100~130 ℃ 0.5~3 minute then, promptly finished the arrangement process.
The present invention has the following advantages:
(1) uses titanium alkoxide and silicon alkoxide to prepare textile finish, adopt and pad or flood the single bath process arrangement, improve the anti-pilling of textiles, uv resistance energy simultaneously.
(2) effect of finishing agent of the present invention is the mating reaction of each reagent, and its consumption can be regulated in the scope of broad, and effect is not had much affect, and makes working condition simplify, and technical process is not harsh.
(3) use this finishing agent and can realize that textiles prevents pilling, the arrangement of anti-ultraviolet, simplified processing technology, reduced consumption, reduced processing cost, improved production efficiency water, the energy by single bath process.
The specific embodiment
The present invention will be further described below in conjunction with specific embodiment.But the present invention is not limited in following embodiment.
Embodiment 1
(1) finishing agent preparation
A. the 1mol butyl titanate is dissolved in the 6mol glacial acetic acid, is made into the glacial acetic acid solution of butyl titanate; 0.03mol hydrochloric acid is dissolved in the 37.5mol pure water, and the glacial acetic acid solution that adds described butyl titanate again stirs, and obtains mixture;
B. 8mol γ-glycidyl ether oxygen propyl trimethoxy silicane is joined in the mixture that obtains among the step a, stir, obtain clear solution;
(2) textile finishing
With pure cotton fabric (2/1 twill, 40 * 40/128 * 60,140g/m 2) in above-mentioned finishing agent, two soak two and roll, liquid carrying rate 80%~90% after 80 ℃ of oven dry, baked 3 minutes at 130 ℃ again.
According to same quadrat method, do not use finishing agent, fabric directly pads water, and preparation is in the same old way.
(3) performance test
According to " the mensuration second portion of GBT 4802.2-2008 textile fabric pilling performance: Martindale's method ", use the anti-pilling performance of M235Martindale ABRASION RESISTANCE and pilling tendency tester (Lars, tin Lay Asia-Pacific (Shenzhen) Co., Ltd) test textiles;
According to " evaluation of GB/T 18830-2009 ultraviolet resistance of fabric ", use Lambda 750UV/VIS Spectrometer (platinum Ai Ermo instrument (Shanghai) Co., Ltd.) test ultraviolet resistance of fabric.
After above-mentioned arrangement, COTTON FABRIC pilling performance and ultraviolet through performance are as shown in table 1, arrangement back sample pilling performance is brought up to 3~4 grades by 1 grade, the UPF value brings up to 146 by 25, through the fabric of finishing agent arrangement gained of the present invention, anti-fluffing and anti-pilling performance and uvioresistant through performance all are largely increased as can be seen.
Performance relatively before and after the arrangement of table 1 embodiment 1 pure cotton fabric
- Pilling performance (level) Ultraviolet through performance (UPF value)
To in the same old way 1 ?25
The arrangement sample 3~4 ?50+
Embodiment 2
(1) finishing agent preparation
A. successively with the 0.06mol formic acid, 1.2mol γ-glycidyl ether oxygen propyl trimethoxy silicane adds in the 68mol water, stirs, and obtains mixture;
B. the 1mol butyl titanate is dissolved in the solution that the 8mol acetylacetone,2,4-pentanedione is made into butyl titanate, the acetylacetone,2,4-pentanedione solution of this butyl titanate is joined in the mixture that obtains among the step a, stir, obtain clear solution;
(2) textile finishing
With 70/30 polyester cotton blending knitted fabric (single face weft plain weave, 18tex, vertical close 85 lines/5 centimetres, horizontal close 68 stringers/5 centimetres, grammes per square metre 175g/m 2) in above-mentioned finishing agent, two soak two and roll, liquid carrying rate 70%~80% after 80 ℃ of oven dry, baked 3 minutes at 130 ℃ again.
According to same quadrat method, do not use finishing agent, fabric directly pads water, and preparation is in the same old way.
(3) performance test
According to " mensuration the 3rd part of GB/T 4802.3-2008 textile fabric pilling performance: balling-up case method ", use the anti-pilling performance of the box balling-up case of YG511A (Ningbo of Zhejiang textile instrument factory) test textiles;
According to " evaluation of GB/T 18830-2009 ultraviolet resistance of fabric ", use Lambda 750UV/VIS Spectrometer (platinum Ai Ermo instrument (Shanghai) Co., Ltd.) test ultraviolet resistance of fabric.
After above-mentioned arrangement, polyester-cotton fabric pilling performance and ultraviolet through performance are as shown in table 2, arrangement back sample pilling performance is brought up to 4~5 grades by 2 grades, the UPF value brings up to 152 by 36, through the fabric of finishing agent arrangement gained of the present invention, anti-fluffing and anti-pilling performance and uvioresistant through performance all are largely increased as can be seen.
70/30 polyester cotton blending knit fabric finishing front and back performance relatively among table 2 embodiment 2
- Pilling performance (level) Ultraviolet through performance (UPF value)
To in the same old way 2 ?36
The arrangement sample 4~5 ?50+

Claims (10)

1. an anti-pilling is prevented the ultraviolet finishing agent, it is characterized in that described finishing agent is made by the method that may further comprise the steps:
(1) the titanium alkoxide is dissolved in the organic solvent, the solution with gained adds in the acidic aqueous solution again, stirs, and obtains mixture;
(2) silicon alkoxide is joined in the mixture that step (1) obtains, stir, obtain clear solution, promptly described finishing agent;
Perhaps make by the method that may further comprise the steps:
(1) acid, silicon alkoxide is soluble in water successively, stir, obtain mixture;
(2) the titanium alkoxide is dissolved in the organic solvent, the solution of gained joins in the mixture that obtains in the step (1), stirs, and obtains clear solution, promptly described finishing agent.
2. finishing agent as claimed in claim 1 is characterized in that:
Described silicon alkoxide is selected from least a in the alkoxy silane of C4~C20;
Described titanium alkoxide is selected from least a in C8~C20 alkoxytitanium acid esters;
Described acid is selected from least a in inorganic acid or the water miscible organic acid;
Described organic solvent is selected from least a in the hydroxyl organic ligand compound.
3. finishing agent as claimed in claim 1 is characterized in that:
Described silicon alkoxide is selected from least a in methyl silicate, ethyl orthosilicate, γ-glycidyl ether oxygen propyl trimethyl oxosilane, vinyl trimethyl oxosilane, vinyl triethyl group oxosilane, γ-(methacryloxy) oxypropyl trimethyl oxosilane.
4. finishing agent as claimed in claim 1 is characterized in that:
Described titanium alkoxide is selected from least a in butyl titanate, metatitanic acid four n-propyls, tetraisopropyl titanate, metatitanic acid four isobutyl esters, the tetraethyl titanate.
5. finishing agent as claimed in claim 1 is characterized in that:
Described acid is selected from least a in hydrochloric acid, nitric acid, the formic acid.
6. finishing agent as claimed in claim 1 is characterized in that:
Described organic solvent is selected from least a in acetic acid, the acetylacetone,2,4-pentanedione.
7. as the described finishing agent of one of claim 1~6, it is characterized in that:
The mol ratio of described titanium alkoxide and water is 1: (1~200);
The mol ratio of described titanium alkoxide and organic solvent is 1: (0.5~100);
Described titanium alkoxide is 1 with the mol ratio of acid: (0.001~10);
The mol ratio of described titanium alkoxide and silicon alkoxide is 1: (0.01~100).
8. finishing agent as claimed in claim 7 is characterized in that:
The mol ratio of described titanium alkoxide and water is 1: (30~100);
The mol ratio of described titanium alkoxide and organic solvent is 1: (4~10);
Described titanium alkoxide is 1 with the mol ratio of acid: (0.01~0.1);
The mol ratio of described titanium alkoxide and silicon alkoxide is 1: (1~10).
9. preparation is characterized in that as the preparation method of the anti-ultraviolet finishing agent of the described anti-pilling of one of claim 1~8 described method may further comprise the steps:
(1) the titanium alkoxide is dissolved in the organic solvent, the solution with gained adds in the acidic aqueous solution again, stirs, and obtains mixture;
(2) silicon alkoxide is joined in the mixture that step (1) obtains, stir, obtain clear solution, promptly described finishing agent;
Perhaps described method may further comprise the steps:
(1) acid, silicon alkoxide is soluble in water successively, stir, obtain mixture;
(2) the titanium alkoxide is dissolved in the organic solvent, the solution of gained joins in the mixture that obtains in the step (1), stirs, and obtains clear solution, promptly described finishing agent.
10. as the purposes of the anti-ultraviolet finishing agent of the described anti-pilling of one of claim 1~8, it is characterized in that:
Described finishing agent is used for pure cotton fabric, or the anti-pilling of the BLENDED FABRIC of chemical fibre and cotton and the arrangement of anti-ultraviolet;
Described chemical fibre is selected from least a in polyester fiber, polyamide fiber, the polypropylene fibre.
CN 201010595876 2010-12-20 2010-12-20 Fuzzing, pilling and ultraviolet-prevention finishing agent and preparation method and application Expired - Fee Related CN102154829B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 201010595876 CN102154829B (en) 2010-12-20 2010-12-20 Fuzzing, pilling and ultraviolet-prevention finishing agent and preparation method and application

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 201010595876 CN102154829B (en) 2010-12-20 2010-12-20 Fuzzing, pilling and ultraviolet-prevention finishing agent and preparation method and application

Publications (2)

Publication Number Publication Date
CN102154829A true CN102154829A (en) 2011-08-17
CN102154829B CN102154829B (en) 2012-11-07

Family

ID=44436488

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 201010595876 Expired - Fee Related CN102154829B (en) 2010-12-20 2010-12-20 Fuzzing, pilling and ultraviolet-prevention finishing agent and preparation method and application

Country Status (1)

Country Link
CN (1) CN102154829B (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103396698A (en) * 2013-07-19 2013-11-20 浙江理工大学 Blue-ray curing formula and textile digital functional finishing method utilizing same
CN104499064A (en) * 2014-12-22 2015-04-08 常熟市金羽纤维制品厂 Anti-pilling shell fabric spinning method
CN106702718A (en) * 2016-12-05 2017-05-24 苏州榕绿纳米科技有限公司 Method for preparing fabric with super wearing resistance, special wettability and anti-ultraviolet function
CN107268269A (en) * 2017-07-27 2017-10-20 江苏工程职业技术学院 A kind of multi-functional crease and shrink resistant finishing liquid and preparation method thereof
CN107287893A (en) * 2017-07-27 2017-10-24 江苏工程职业技术学院 A kind of method for sorting of multi-functional cotton wash-and-wear fabrics
CN109235023A (en) * 2018-08-31 2019-01-18 黄勇 A kind of preparation method of high-affinity Anti-ultraviolet true silk textile finishing agent material
CN115652617A (en) * 2022-11-15 2023-01-31 苏州联胜化学有限公司 Anti-infrared anti-pilling agent and preparation method thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57161166A (en) * 1981-03-26 1982-10-04 Toray Industries Treatment of polyester fiber
CN1631996A (en) * 2004-12-07 2005-06-29 中国科学院山西煤炭化学研究所 Method for preparing silicon oxide/titanium dioxide composite oxide ultraviolet screening agent
CN101363190A (en) * 2008-09-26 2009-02-11 江南大学 Preparation of gemini type composite colloidal sols and applications thereof in UV-preventing and anti-bacteria finishing
CN101503859A (en) * 2008-02-04 2009-08-12 上海德桑精细化工有限公司 Anti-fuzzing and anti-pilling finishing agent for fabric
CN101768854A (en) * 2009-12-29 2010-07-07 陕西科技大学 Freon-free super hydrophobic UV resistant cotton fabric and method for preparing same

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57161166A (en) * 1981-03-26 1982-10-04 Toray Industries Treatment of polyester fiber
CN1631996A (en) * 2004-12-07 2005-06-29 中国科学院山西煤炭化学研究所 Method for preparing silicon oxide/titanium dioxide composite oxide ultraviolet screening agent
CN101503859A (en) * 2008-02-04 2009-08-12 上海德桑精细化工有限公司 Anti-fuzzing and anti-pilling finishing agent for fabric
CN101363190A (en) * 2008-09-26 2009-02-11 江南大学 Preparation of gemini type composite colloidal sols and applications thereof in UV-preventing and anti-bacteria finishing
CN101768854A (en) * 2009-12-29 2010-07-07 陕西科技大学 Freon-free super hydrophobic UV resistant cotton fabric and method for preparing same

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103396698A (en) * 2013-07-19 2013-11-20 浙江理工大学 Blue-ray curing formula and textile digital functional finishing method utilizing same
CN104499064A (en) * 2014-12-22 2015-04-08 常熟市金羽纤维制品厂 Anti-pilling shell fabric spinning method
CN106702718A (en) * 2016-12-05 2017-05-24 苏州榕绿纳米科技有限公司 Method for preparing fabric with super wearing resistance, special wettability and anti-ultraviolet function
CN106702718B (en) * 2016-12-05 2019-05-14 苏州榕绿纳米科技有限公司 A kind of special wellability uvioresistant function fabric construction method of super abrasive
CN107268269A (en) * 2017-07-27 2017-10-20 江苏工程职业技术学院 A kind of multi-functional crease and shrink resistant finishing liquid and preparation method thereof
CN107287893A (en) * 2017-07-27 2017-10-24 江苏工程职业技术学院 A kind of method for sorting of multi-functional cotton wash-and-wear fabrics
CN107287893B (en) * 2017-07-27 2019-11-26 江苏工程职业技术学院 A kind of method for sorting of multi-functional cotton wash-and-wear fabrics
CN109235023A (en) * 2018-08-31 2019-01-18 黄勇 A kind of preparation method of high-affinity Anti-ultraviolet true silk textile finishing agent material
CN115652617A (en) * 2022-11-15 2023-01-31 苏州联胜化学有限公司 Anti-infrared anti-pilling agent and preparation method thereof

Also Published As

Publication number Publication date
CN102154829B (en) 2012-11-07

Similar Documents

Publication Publication Date Title
CN102154829B (en) Fuzzing, pilling and ultraviolet-prevention finishing agent and preparation method and application
CN107326651B (en) Multi-functional super-hydrophobic textile finishing agent, preparation method and application
CN101591854B (en) Nano durable super hydrophobicity finishing method for cellulose fabric
CN102251391B (en) Method for superhydrophobic finishing of textile
CN101270547B (en) Method for processing nano-function textile
CN106381714B (en) Preparation method with fire-retardant and hydrophobic function fabric
CN103806262B (en) A kind of preparation method of automatically cleaning wool fabric
CN102021819A (en) Fluorine-free superhydrophobic finishing agent containing modified nano silicon dioxide hydrosol and application thereof
CN108755125B (en) Flame-retardant anti-ultraviolet nylon fabric and preparation method thereof
CN1936168A (en) Fabric product finishing agent and its preparing process and method thereof
CN106756935A (en) A kind of vitrified agent for improving metal corrosion-resisting, preparation method and its application method
CN106700788A (en) Nano environment-friendly and heat insulation transparent paint and preparation method thereof
CN109019616A (en) A kind of preparation and application of silica/molybdenum disulfide three-dimensional hybrid material
CN108238729A (en) A kind of silane coupler modified basalt fibre and preparation method thereof
CN105803760A (en) Titanium dioxide textile and preparation method thereof
CN114672157B (en) Halogen-free flame-retardant master batch for glass fiber reinforced nylon, and preparation method and application thereof
CN105734964A (en) Textile auxiliary agent for auxiliary textile sizing and preparation method thereof
CN109468860B (en) Preparation method of Zn-MOF-based multifunctional dyed polyester fabric
CN109914108B (en) Fluorine-free water repellent finishing method for polyester fabric
CN106884313A (en) A kind of worsted fabric sol-gal process water-repellent finishing method
CN105484037B (en) The preparation method of fabric step treating reagent containing nitrogen phosphorus silicon
CN111423463B (en) Preparation method and application of reactive boron-containing flame retardant
CN105350288A (en) Finishing agent for fabric with antistatic property and self-cleaning function and preparation method of finishing agent
CN102587137A (en) Novel environment-friendly energy saving spinning sizing agent and preparation method thereof
CN110004509B (en) Colored flame-retardant fiber and preparation method 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
C14 Grant of patent or utility model
GR01 Patent grant
ASS Succession or assignment of patent right

Owner name: LANCY CO., LTD.

Free format text: FORMER OWNER: BEIJING INSTITUTE OF FASHION TECHNOLOGY

Effective date: 20131219

C41 Transfer of patent application or patent right or utility model
COR Change of bibliographic data

Free format text: CORRECT: ADDRESS; FROM: 100029 CHAOYANG, BEIJING TO: 101319 SHUNYI, BEIJING

TR01 Transfer of patent right

Effective date of registration: 20131219

Address after: 101319, 63, Bai Bai Road, Ma Ma Town, Beijing, Shunyi District

Patentee after: LANCY CO.,LTD.

Address before: 100029 Beijing city Chaoyang District Heping Street North Sakura Road No. 2

Patentee before: Beijing Institute of Fashion Technology

DD01 Delivery of document by public notice

Addressee: LANCY CO.,LTD.

Document name: Notification of Decision on Request for Restoration of Right

CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20121107

Termination date: 20211220

CF01 Termination of patent right due to non-payment of annual fee