CN109235023A - A kind of preparation method of high-affinity Anti-ultraviolet true silk textile finishing agent material - Google Patents

A kind of preparation method of high-affinity Anti-ultraviolet true silk textile finishing agent material Download PDF

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Publication number
CN109235023A
CN109235023A CN201811014802.2A CN201811014802A CN109235023A CN 109235023 A CN109235023 A CN 109235023A CN 201811014802 A CN201811014802 A CN 201811014802A CN 109235023 A CN109235023 A CN 109235023A
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parts
agent material
finishing agent
ultraviolet
stirred
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黄勇
韩桂林
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    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M11/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
    • D06M11/32Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
    • D06M11/36Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
    • D06M11/46Oxides or hydroxides of elements of Groups 4 or 14 of the Periodic Table; Titanates; Zirconates; Stannates; Plumbates
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M11/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
    • D06M11/77Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with silicon or compounds thereof
    • D06M11/79Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with silicon or compounds thereof with silicon dioxide, silicic acids or their salts
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/50Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with organometallic compounds; with organic compounds containing boron, silicon, selenium or tellurium atoms
    • D06M13/51Compounds with at least one carbon-metal or carbon-boron, carbon-silicon, carbon-selenium, or carbon-tellurium bond
    • D06M13/513Compounds with at least one carbon-metal or carbon-boron, carbon-silicon, carbon-selenium, or carbon-tellurium bond with at least one carbon-silicon bond
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/285Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acid amides or imides
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/327Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated alcohols or esters thereof
    • D06M15/333Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated alcohols or esters thereof of vinyl acetate; Polyvinylalcohol
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/507Polyesters
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2101/00Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
    • D06M2101/02Natural fibres, other than mineral fibres
    • D06M2101/10Animal fibres
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/25Resistance to light or sun, i.e. protection of the textile itself as well as UV shielding materials or treatment compositions therefor; Anti-yellowing treatments

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Organic Chemistry (AREA)
  • Silicon Polymers (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

The present invention relates to a kind of preparation methods of high-affinity Anti-ultraviolet true silk textile finishing agent material, belong to textile material technical field.Technical solution of the present invention uses collosol and gel composite algorithm, it is compound using ethyl orthosilicate and butyl titanate and prepare modified nano-titanium dioxide, increase strong suction-operated of the titanium dioxide surface acidic site to organic matter by polymer overmold and by silica, stronger group is formed on surface, polymer overmold is modified simultaneously, improves the bond strength between textile finishing agent material and fabric;And the present invention is during forming nanometer titanium dioxide titanium gel, processing is modified by adding amino-compound, through condensation reaction, nanoscale cluster is caused to be formed, along with the insertion or absorption of organic group, so that its structure is formd steric hindrance, can effectively prevent the reunion of nanometer titanic oxide material in the hydro-thermal stage in later period, effectively improve the uniform and stable performance of composite finishing agent material.

Description

A kind of preparation method of high-affinity Anti-ultraviolet true silk textile finishing agent material
Technical field
The present invention relates to a kind of preparation methods of high-affinity Anti-ultraviolet true silk textile finishing agent material, belong to textile material Technical field.
Background technique
Silk possesses its excellent performance as a kind of azelon, such as soft, the ventilative and good parent of moisture absorption
The features such as skin.However, cocoon fiber is to sunlight UV radiation-sensitive, although itself has faint uvioresistant Performance, however under sunlight irradiation, real silk fabric will be by irreversible damage.Modern society for silk needs Through being not limited only to indoor wear, as a large amount of silk dress ornaments use outdoors, people are aobvious for the efficient uvioresistant performance of silk It obtains more urgent.In order to overcome this problem, many methods have been used to influence the anti-ultraviolet property of silk.
In recent years, excessive ultraviolet light irradiation has caused the concern of people to the harm of human body, and nano-titanium dioxide then may be used Effectively to shield the UVA and UVB that can cause harm to the human body in daylight.Super oxidability can possessed by titanium dioxide The cell membrane of cell is destroyed, so that cellular component loss be made to cause bacterial death;The also protein of solidifiable virus inhibits virus Activity achievees the purpose that inactivation of viruses.Being arranged using nano-titanium dioxide to fabric can obtain having a variety of excellent performances Function textile nano-TiO2As a kind of important N-type semiconductor material, since its special performance makes it in various necks Domain is such as catalyzed, and solar battery, chemical sensor, UV absorption and opto-electronic device etc. have a wide range of applications.So And, it is contemplated that nano-TiO2Particle surface lacks active group, how effectively to provide active group abundant on its surface, Realize TiO2Nanoparticle is effectively combined with organic or inorganic media implementation, is the key that existing improvement preparation arranges agent material.
Summary of the invention
The technical problems to be solved by the invention: for nano-TiO in existing gas Silk Fabric Finishing agent material2Particle table Face lacks active group, and the bad problem of compatibility between fabric provides a kind of high-affinity Anti-ultraviolet true silk textile finishing The preparation method of agent material.
In order to solve the above technical problems, the technical solution adopted by the present invention is that:
(1) according to parts by weight, 45~50 parts of tetrahydrofurans, 3~5 parts of acrylamides, 3~5 parts of polylactic acid, 1~2 are weighed respectively Part vinylacetate and 1~2 part of azodiisobutyronitrile are placed in a beaker, and are stirred and are collected lysate;
(2) 3- aminopropyl-trimethoxy silane is added dropwise in lysate by 1:10 in mass ratio, after being added dropwise to complete, stirring It mixes and collects to obtain modification liquid, according to parts by weight, weigh 45~50 parts of modification liquids, 10~15 parts of citric acids and 25~30 respectively Part epoxychloropropane is placed in a beaker, and is stirred and insulation reaction, standing are cooled to room temperature, collect to obtain reaction solution;
(3) butyl titanate and ethyl orthosilicate are stirred and are collected matrix liquid, in mass ratio 1:5 by 1:2 in mass ratio, Matrix drop is added in reaction solution, after being added dropwise to complete, collects to obtain composite modified liquid;
(4) according to parts by weight, respectively weigh 45~50 parts of composite modified liquid, 3~5 parts of mass fraction 10%HCl solution, 35~ 40 parts of deionized waters and 10~15 parts of tetrahydrofurans are placed in conical flask, are stirred and are placed in mold, mold are used poly- Polypropylene film seals and stands 2~3 days, handles the polypropylene film bundle hole of sealing and stands 10~15 days, can be prepared into The high-affinity anti-UV fabric arranges agent material.
3- aminopropyl-trimethoxy silane drop rate described in step (2) is 2~3mL/min.
Matrix drop rate of acceleration described in step (3) is 3~5mL/min.
Film described in step (4) pricks hole processing to prick hole processing to the polypropylene film of sealing by 200/m2 of hole count is pricked.
The present invention is compared with other methods, and advantageous effects are:
(1) technical solution of the present invention uses collosol and gel composite algorithm, compound using ethyl orthosilicate and butyl titanate and prepare Modified nano-titanium dioxide increases titanium dioxide surface acidic site to organic matter by polymer overmold and by silica Strong suction-operated forms stronger group on surface, while effectively preparation has answering for lesser partial size and high specific surface area Condensation material, while polymer overmold is modified, improves the compatibility between material and organic phase material, improves textile finishing agent material Bond strength between fabric;
(2) technical solution of the present invention is changed during forming nanometer titanium dioxide titanium gel by adding amino-compound Property processing, through condensation reaction, nanoscale cluster is caused to be formed, along with the insertion or absorption of organic group, makes its structure shape At steric hindrance, it can effectively prevent the reunion of nanometer titanic oxide material in the hydro-thermal stage in later period, effectively improve composite finishing The uniform and stable performance of agent material.
Specific embodiment
According to parts by weight, respectively weigh 45~50 parts of tetrahydrofurans, 3~5 parts of acrylamides, 3~5 parts of polylactic acid, 1~ 2 parts of vinylacetates and 1~2 part of azodiisobutyronitrile are placed in a beaker, and are stirred and collect lysate, in mass ratio 1: 10,3- aminopropyl-trimethoxy silane is added dropwise in lysate, control drop rate is 2~3mL/min, wait drip Cheng Hou is stirred and collects to obtain modification liquid;According to parts by weight, 45~50 parts of modification liquids, 10~15 portions of lemons are weighed respectively Acid and 25~30 parts of epoxychloropropane are placed in a beaker, and are stirred and are placed in 2~3h of insulation reaction at 75~80 DEG C, are stood cold But to room temperature, reaction solution is collected to obtain;Butyl titanate and ethyl orthosilicate are stirred and collect matrix by 1:2 in mass ratio Liquid, in mass ratio 1:5 add to matrix drop in reaction solution, and control drop rate is 3~5mL/min, after being added dropwise to complete, Composite modified liquid is collected to obtain, according to parts by weight, weighs 45~50 parts of composite modified liquid, 3~5 parts of mass fractions 10% respectively HCl solution, 35~40 parts of deionized waters and 10~15 parts of tetrahydrofurans are placed in conical flask, at 3500~4000r/min It is stirred and is placed in mold, mold polypropylene film is sealed and stand 2~3 days, by bundle 200/m of hole count2, to envelope The polypropylene film of mouth pricks hole and handles and stand 10~15 days, and it is whole can be prepared into the high-affinity Anti-ultraviolet true silk fabric Manage agent material.
According to parts by weight, 45 parts of tetrahydrofurans, 3 parts of acrylamides, 3 parts of polylactic acid, 1 part of vinylacetate are weighed respectively It is placed in a beaker with 1 part of azodiisobutyronitrile, is stirred and collects lysate, in mass ratio 1:10, by 3- aminopropyl- Trimethoxy silane is added dropwise in lysate, and control drop rate is that 2mL/min is stirred and collects after being added dropwise to complete Obtain modification liquid;According to parts by weight, 45 parts of modification liquids, 10 parts of citric acids and 25 parts of epoxychloropropane are weighed respectively be placed in beaker In, it is stirred and is placed in insulation reaction 2h, standing at 75 DEG C and is cooled to room temperature, collect to obtain reaction solution;1:2 in mass ratio, will Butyl titanate and ethyl orthosilicate are stirred and collect matrix liquid, in mass ratio 1:5, and matrix drop is added to reaction solution In, control drop rate be 3mL/min, after being added dropwise to complete, collect composite modified liquid weighs respectively according to parts by weight 45 parts of composite modified liquid, 3 parts of mass fraction 10%HCl solution, 35 parts of deionized waters and 10 parts of tetrahydrofurans are placed in conical flask In, it is stirred and is placed in mold at 3500r/min, mold polypropylene film is sealed and stands 2 days, by bundle hole count 200/m2, the polypropylene film bundle hole of sealing is handled and stands 10 days, the high-affinity uvioresistant can be prepared into Silk Fabric Finishing agent material.
According to parts by weight, 47 parts of tetrahydrofurans, 4 parts of acrylamides, 4 parts of polylactic acid, 2 parts of vinylacetates are weighed respectively It is placed in a beaker with 2 parts of azodiisobutyronitriles, is stirred and collects lysate, in mass ratio 1:10, by 3- aminopropyl- Trimethoxy silane is added dropwise in lysate, and control drop rate is that 2mL/min is stirred and collects after being added dropwise to complete Obtain modification liquid;According to parts by weight, 47 parts of modification liquids, 12 parts of citric acids and 27 parts of epoxychloropropane are weighed respectively be placed in beaker In, it is stirred and is placed in insulation reaction 2h, standing at 77 DEG C and is cooled to room temperature, collect to obtain reaction solution;1:2 in mass ratio, will Butyl titanate and ethyl orthosilicate are stirred and collect matrix liquid, in mass ratio 1:5, and matrix drop is added to reaction solution In, control drop rate be 4mL/min, after being added dropwise to complete, collect composite modified liquid weighs respectively according to parts by weight 47 parts of composite modified liquid, 4 parts of mass fraction 10%HCl solution, 37 parts of deionized waters and 12 parts of tetrahydrofurans are placed in conical flask In, it is stirred and is placed in mold at 3750r/min, mold polypropylene film is sealed and stands 2 days, by bundle hole count 200/m2, the polypropylene film bundle hole of sealing is handled and stands 12 days, the high-affinity uvioresistant can be prepared into Silk Fabric Finishing agent material.
According to parts by weight, 50 parts of tetrahydrofurans, 5 parts of acrylamides, 5 parts of polylactic acid, 2 parts of vinylacetates are weighed respectively It is placed in a beaker with 2 parts of azodiisobutyronitriles, is stirred and collects lysate, in mass ratio 1:10, by 3- aminopropyl- Trimethoxy silane is added dropwise in lysate, and control drop rate is that 3mL/min is stirred and collects after being added dropwise to complete Obtain modification liquid;According to parts by weight, 50 parts of modification liquids, 15 parts of citric acids and 30 parts of epoxychloropropane are weighed respectively be placed in beaker In, it is stirred and is placed in insulation reaction 3h, standing at 80 DEG C and is cooled to room temperature, collect to obtain reaction solution;1:2 in mass ratio, will Butyl titanate and ethyl orthosilicate are stirred and collect matrix liquid, in mass ratio 1:5, and matrix drop is added to reaction solution In, control drop rate be 5mL/min, after being added dropwise to complete, collect composite modified liquid weighs respectively according to parts by weight 50 parts of composite modified liquid, 5 parts of mass fraction 10%HCl solution, 40 parts of deionized waters and 15 parts of tetrahydrofurans are placed in conical flask In, it is stirred and is placed in mold at 4000r/min, mold polypropylene film is sealed and stands 3 days, by bundle hole count 200/m2, the polypropylene film bundle hole of sealing is handled and stands 15 days, the high-affinity uvioresistant can be prepared into Silk Fabric Finishing agent material.
Example 1,2,3 prepared by the present invention is tested for the property, specific test result is as follows shown in table table 1:
1 performance test table of table
As seen from the above table, arrangement agent material prepared by the present invention between fabric have excellent bond strength.

Claims (4)

1. a kind of preparation method of high-affinity Anti-ultraviolet true silk textile finishing agent material, it is characterised in that specific preparation step Are as follows:
(1) according to parts by weight, 45~50 parts of tetrahydrofurans, 3~5 parts of acrylamides, 3~5 parts of polylactic acid, 1~2 are weighed respectively Part vinylacetate and 1~2 part of azodiisobutyronitrile are placed in a beaker, and are stirred and are collected lysate;
(2) 3- aminopropyl-trimethoxy silane is added dropwise in lysate by 1:10 in mass ratio, after being added dropwise to complete, stirring It mixes and collects to obtain modification liquid, according to parts by weight, weigh 45~50 parts of modification liquids, 10~15 parts of citric acids and 25~30 respectively Part epoxychloropropane is placed in a beaker, and is stirred and insulation reaction, standing are cooled to room temperature, collect to obtain reaction solution;
(3) butyl titanate and ethyl orthosilicate are stirred and are collected matrix liquid, in mass ratio 1:5 by 1:2 in mass ratio, Matrix drop is added in reaction solution, after being added dropwise to complete, collects to obtain composite modified liquid;
(4) according to parts by weight, respectively weigh 45~50 parts of composite modified liquid, 3~5 parts of mass fraction 10%HCl solution, 35~ 40 parts of deionized waters and 10~15 parts of tetrahydrofurans are placed in conical flask, are stirred and are placed in mold, mold are used poly- Polypropylene film seals and stands 2~3 days, handles the polypropylene film bundle hole of sealing and stands 10~15 days, can be prepared into The high-affinity anti-UV fabric arranges agent material.
2. a kind of preparation method of high-affinity Anti-ultraviolet true silk textile finishing agent material according to claim 1, special Sign is: 3- aminopropyl-trimethoxy silane drop rate described in step (2) is 2~3mL/min.
3. a kind of preparation method of high-affinity Anti-ultraviolet true silk textile finishing agent material according to claim 1, special Sign is: matrix drop rate of acceleration described in step (3) is 3~5mL/min.
4. a kind of preparation method of high-affinity Anti-ultraviolet true silk textile finishing agent material according to claim 1, special Sign is: film described in step (4) pricks hole processing to prick hole processing to the polypropylene film of sealing by 200/m2 of hole count is pricked.
CN201811014802.2A 2018-08-31 2018-08-31 A kind of preparation method of high-affinity Anti-ultraviolet true silk textile finishing agent material Pending CN109235023A (en)

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Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
CN1699488A (en) * 2005-05-27 2005-11-23 吉林大学 High strength organic / inorganic nano composite transparent film layer materials and method for preparing same
CN102154829A (en) * 2010-12-20 2011-08-17 北京服装学院 Fuzzing, pilling and ultraviolet-prevention finishing agent and preparation method and application
CN102191629A (en) * 2010-03-17 2011-09-21 科德宝·波利泰克斯股份公司 Nonwoven product containing organic and/or mineral particles and its method of manufacturing
CN103464214A (en) * 2013-08-22 2013-12-25 徐州工程学院 Modified nano TiO2 photocatalyst capable of degrading benzene series, and preparation method and application of same
CN105019225A (en) * 2015-08-06 2015-11-04 苏州丝之源纺织科技有限公司 Preparation method for silk quilt inner capable of generating anions
CN105601949A (en) * 2016-01-13 2016-05-25 陕西科技大学 TiO2-SiO2 co-modified casein composite emulsion and method for preparing same
CN105603727A (en) * 2016-01-08 2016-05-25 湖州市千金丝织厂 Novel anti-ultraviolet antibacterial finishing agent and preparing method thereof
CN107090200A (en) * 2017-04-21 2017-08-25 周益铭 A kind of preparation method of ultraviolet light screener
US20180016736A1 (en) * 2015-11-24 2018-01-18 Domac Llc. Composition for fiber adhesion and fabrics using the same

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
CN1699488A (en) * 2005-05-27 2005-11-23 吉林大学 High strength organic / inorganic nano composite transparent film layer materials and method for preparing same
CN102191629A (en) * 2010-03-17 2011-09-21 科德宝·波利泰克斯股份公司 Nonwoven product containing organic and/or mineral particles and its method of manufacturing
CN102154829A (en) * 2010-12-20 2011-08-17 北京服装学院 Fuzzing, pilling and ultraviolet-prevention finishing agent and preparation method and application
CN103464214A (en) * 2013-08-22 2013-12-25 徐州工程学院 Modified nano TiO2 photocatalyst capable of degrading benzene series, and preparation method and application of same
CN105019225A (en) * 2015-08-06 2015-11-04 苏州丝之源纺织科技有限公司 Preparation method for silk quilt inner capable of generating anions
US20180016736A1 (en) * 2015-11-24 2018-01-18 Domac Llc. Composition for fiber adhesion and fabrics using the same
CN105603727A (en) * 2016-01-08 2016-05-25 湖州市千金丝织厂 Novel anti-ultraviolet antibacterial finishing agent and preparing method thereof
CN105601949A (en) * 2016-01-13 2016-05-25 陕西科技大学 TiO2-SiO2 co-modified casein composite emulsion and method for preparing same
CN107090200A (en) * 2017-04-21 2017-08-25 周益铭 A kind of preparation method of ultraviolet light screener

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