CN106120339B - Fabric and preparation method and purposes in a kind of air and oil with ultra-hydrophobicity - Google Patents

Fabric and preparation method and purposes in a kind of air and oil with ultra-hydrophobicity Download PDF

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CN106120339B
CN106120339B CN201610525568.4A CN201610525568A CN106120339B CN 106120339 B CN106120339 B CN 106120339B CN 201610525568 A CN201610525568 A CN 201610525568A CN 106120339 B CN106120339 B CN 106120339B
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fabric
hydrophobicity
preparation
ultra
oil
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CN106120339A (en
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朱小涛
任桂娜
宋远明
闫京勇
王玉燕
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Yantai University
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Yantai University
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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
    • 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
    • D06M15/244Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of halogenated hydrocarbons
    • D06M15/256Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of halogenated hydrocarbons containing fluorine
    • 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
    • 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
    • D06M2101/04Vegetal fibres
    • D06M2101/06Vegetal fibres cellulosic
    • 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
    • D06M2101/16Synthetic fibres, other than mineral fibres
    • D06M2101/30Synthetic polymers consisting of macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M2101/32Polyesters
    • 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
    • D06M2200/10Repellency against liquids
    • D06M2200/12Hydrophobic properties

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Materials Applied To Surfaces To Minimize Adherence Of Mist Or Water (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)

Abstract

The invention discloses one kind to have ultra-hydrophobicity fabric and its preparation method and application in air and oil.This method soaks the fabric into the toluene solution containing alkylation silica and Polytetrafluoroethylene emulsion, then takes out fabric from solution, and superhydrophobic fabric is obtained after heating, drying.Droplet is greater than 150 in the contact angle of gained fabrico, and easily tumbled from fabric surface.The fabric through finger touch, blade scribing and repeatedly with after sand paper opposite grinding still have excellent ultra-hydrophobicity.Moreover, still showing excellent ultra-hydrophobicity when gained fabric is dipped in oil.It is the superhydrophobic fabric preparation method simple process, mild condition, low in cost.

Description

Fabric and preparation method and purposes in a kind of air and oil with ultra-hydrophobicity
Technical field
The present invention relates to a kind of superhydrophobic fabrics and its preparation method and application, specifically prepare one kind using infusion process and exist The fabric of ultra-hydrophobicity is all had in air and in oil, to expand the use scope of superhydrophobic fabric.
Background technique
Superhydrophobic fabric is increasingly subject to the favor of people, is current function by performances such as its unique automatically cleaning, antipollutions One of the hot spot of energy textile.Researcher has passed through nanometer particle load method (Chinese invention patent CN102321974A), has connect Branch polymeric method (Adv. Mater. 2010,22,5473-5477), sol-gel method (Chinese invention patent ) etc. CN102277720A it is prepared for a large amount of superhydrophobic fabrics.However, these preparation superhydrophobic fabrics mechanical endurance compared with Difference, after by friction, even finger is touched, fabric is easy to lose ultra-hydrophobicity.It is durable in order to solve superhydrophobic fabric machinery Property difference problem, researchers at home and abroad have carried out a series of exploratory developments.Such as: Chinese invention patent CN103074768A is logical It crosses lye etching and low-surface energy substance modification is prepared for the super-hydrophobic dacron of wash resistant and rub resistance.S. Seeger etc. People is by being prepared for stable ultra-hydrophobic fabric in fabric surface growth in situ silicon nanowires.But these methods also have Disadvantage, such as preparation process are relatively complicated, need expensive chemicals and particular instrument.Therefore, develop a kind of simple, economical Method seem particularly significant to prepare durable super-hydrophobic property fabric just.
The ring that when if superhydrophobic fabric is in oil environment still there is ultra-hydrophobicity superhydrophobic fabric will be greatly improved Border durability, and the added value and practicability of superhydrophobic fabric can be greatly improved, surpass its application range to widen.But mesh Preceding resulting fabric only has ultra-hydrophobicity in air, and there are no the research reports about superhydrophobic fabric in oil.Cause This, invention in the oil superhydrophobic fabric be it is extremely necessary, also there is important meaning for the promotion and application of superhydrophobic fabric Justice and have potential great market.
Summary of the invention
The present invention solves the problems, such as that superhydrophobic fabric stability exists the prior art, provides a kind of durable super-hydrophobic property and knits Object and its preparation method and application, it is the method simple process, low in cost, reproducible.
There is ultra-hydrophobicity fabric and its preparation method and application in the oil it is a further object of the present invention to provide a kind of, To improve the application range of superhydrophobic fabric.
The preparation method of the fabric of ultra-hydrophobicity is all had in a kind of air provided by the present invention and in oil, including such as Lower step:
The preparation of A alkylation silica:
Under room temperature, organochlorosilane is added dropwise into the toluene solution uniformly containing silica dioxide granule, then magnetic agitation 6h;
To after reaction, centrifugal treating simultaneously removes supernatant, then being removed using ethanol washing product unreacted is had Machine chlorosilane, again centrifugal treating obtain alkylation silica dioxide granule after desciccate at 70 DEG C;
The mass ratio of silica used, organochlorosilane and toluene is 1:0.5 ~ 1:35 in the step;
Organochlorosilane used is any one in trichlorine octadecylsilane or trim,ethylchlorosilane in the step;
The preparation of B alkylation silicon dioxide-poly tetrafluoro wax toluene solution:
Silica dioxide granule will be alkylated and Polytetrafluoroethylene emulsion particle is added in toluene, magnetic agitation 1h makes to be alkylated under room temperature Silica and Polytetrafluoroethylene emulsion are uniformly dispersed in toluene, obtain alkylation silicon dioxide-poly tetrafluoro wax toluene solution;
Alkylation silica used in the step, Polytetrafluoroethylene emulsion and toluene mass ratio be 4~1.5:1:85;
The preparation of C superhydrophobic fabric:
Soak the fabric into alkylation silicon dioxide-poly tetrafluoro wax toluene solution and take out after 1 ~ 30min, then 108 ~ After drying removes toluene at 150 DEG C, the fabric that ultra-hydrophobicity is all had in air and in oil is obtained.
It is preferred that the partial size of silica used in step A is 5~70 nanometers.
It is preferred that the partial size of Polytetrafluoroethylene emulsion used in step B is 5~15 microns.
It is preferred that the drying temperature of step C is that effect is optimal at 130 DEG C.
It is preferred that any one in dacron fabric or cotton fibre fabric of the fabric used selected from commercialization.
It is super the present invention also provides being all had in a kind of air being prepared using made as described above method and in oil The fabric of hydrophobic performance.
The fabric that ultra-hydrophobicity is all had in air prepared by the present invention and in oil can be applied in water or in oil.
The superhydrophobic fabric as made from this method, contact angle of the droplet on its surface is 155.5o~158 o, roll angle It is 5 o~7 o
The surface free energy of fabric surface can be reduced the principle of the invention lies in Polytetrafluoroethylene emulsion and alkyl can be enhanced Change the adhesive force between silica and fabric fibre.Roughness and further can be improved in alkylation silica Reduce the surface energy of fabric surface.The roughness of the too high levels of Polytetrafluoroethylene emulsion, fabric surface will reduce, and fabric cannot achieve sky Gas neutralizes ultra-hydrophobicity in oil.The too high levels of silica are alkylated, the adhesive force decline between fabric fibre is knitted Object cannot achieve lasting ultra-hydrophobicity.
After fabric surface impregnates Polytetrafluoroethylene emulsion and alkylation silica, it is heated.Heat treatment temperature Degree, which is higher than 108 DEG C of fusing point of Polytetrafluoroethylene emulsion, makes its melting, and such Polytetrafluoroethylene emulsion will be wrapped in fabric fibre melt surface It is alkylated silica, thus improve Polytetrafluoroethylene emulsion and be alkylated adhesion strength of the silica on fabric fibre surface, this Fabric prepared by sample will show stable ultra-hydrophobicity.When heating temperature is lower than the fusing point of Polytetrafluoroethylene emulsion, although Fabric can show ultra-hydrophobicity, but its ultra-hydrophobicity and unstable, be easy to lose under the effect of external force.
The positive effect of the present invention is that:
1, superhydrophobic fabric of the invention through finger touch, blade scribing and with after 30 opposite grindings of sand paper (pressure at right angle, Friction velocity), 150 are still greater than with the contact angle of water droplet o
2, superhydrophobic fabric preparation method simple process of the invention, preparation cost is cheap, does not need specific instrument sets It is standby.
3, superhydrophobic fabric preparation method of the invention is not limited by fabric substrate type, to cotton, terylene and other fabrics All adapt to.
4, superhydrophobic fabric of the invention still has ultra-hydrophobicity in oil environment.
Detailed description of the invention
Fig. 1 be the made sample of the embodiment of the present invention 1 through with the optical photograph after 30 opposite grindings of sand paper.
Fig. 2 is the made sample of the embodiment of the present invention 1 in dimethicone ultra-hydrophobicity optical photograph.
Specific embodiment
Embodiment 1:
It is alkylated the preparation of silica
Under room temperature, the 0.5g silica dioxide granule that partial size is 5~70 nanometers is added in 20ml toluene, ultrasonic disperse After 15min, 0.5g trichlorine octadecylsilane is added dropwise in above-mentioned dispersion in whipping process, continues to stir 6h.Instead After answering, centrifugal treating removes supernatant.Ethanol washing product is to remove unreacted trichlorine octadecylsilane, at centrifugation It manages, alkylation silica dioxide granule is obtained after dry at 70 DEG C.
It is alkylated the preparation of silicon dioxide-poly tetrafluoro wax toluene solution
0.2g is alkylated the Polytetrafluoroethylene emulsion particle that silica dioxide granule and 0.05g partial size are 5~15 microns, 20ml is added In toluene, magnetic agitation 1h makes to be alkylated silica under room temperature and Polytetrafluoroethylene emulsion is uniformly dispersed in toluene, is alkylated Silicon dioxide-poly tetrafluoro wax toluene solution;
The preparation of superhydrophobic fabric
Dacron is immersed in 1min in alkylation silicon dioxide-poly tetrafluoro wax toluene solution, by dacron from upper It states in solution and takes out, 30min is dried at 130 DEG C to remove toluene, obtains super-hydrophobic dacron.
The contact angle for obtaining superhydrophobic fabric and water droplet is 158 o, roll angle 5 o.Through finger touch, blade scribing and With (pressure at right angle 7N, frictional distance 30cm, friction velocity 3cm/s) after 30 opposite grindings of sand paper, the contact angle with water droplet is 152o, roll angle 14 o.When obtained superhydrophobic fabric is immersed in dimethicone, contact angle of the water droplet on its surface It is 163 o
Embodiment 2:
It is alkylated the preparation of silica
Under room temperature, the 0.5g silica dioxide granule that partial size is 5~70 nanometers is added in 20ml toluene, ultrasonic disperse After 15min, 0.5g trim,ethylchlorosilane is added dropwise in above-mentioned dispersion in whipping process, continues to stir 6h.Reaction knot Shu Hou, centrifugal treating remove supernatant.Ethanol washing product is to remove unreacted trim,ethylchlorosilane, centrifugal treating, and 70 DEG C Alkylation silica dioxide granule is obtained after lower drying.
It is alkylated the preparation of silicon dioxide-poly tetrafluoro wax toluene solution
0.15g is alkylated the Polytetrafluoroethylene emulsion particle that silica dioxide granule and 0.05g partial size are 5~15 microns to be added In 20ml toluene, magnetic agitation 1h makes to be alkylated silica under room temperature and Polytetrafluoroethylene emulsion is uniformly dispersed in toluene, obtains alkane Base silicon dioxide-poly tetrafluoro wax toluene solution;
The preparation of superhydrophobic fabric
Dacron is immersed in 5min in alkylation silicon dioxide-poly tetrafluoro wax toluene solution, by dacron from upper It states in solution and takes out, 30min is dried at 130 DEG C to remove toluene, obtains super-hydrophobic dacron.
The contact angle for obtaining superhydrophobic fabric and water droplet is 157 o, roll angle 6.8 o.Through finger touch, blade scribing, And with (pressure at right angle 7N, frictional distance 30cm, friction velocity 3cm/s) after 30 opposite grindings of sand paper, the contact angle with water droplet is 151.5o, roll angle 15 o.When obtained superhydrophobic fabric is immersed in dimethicone, contact of the water droplet on its surface Angle is 161.5 o
Embodiment 3:
It is alkylated the preparation of silica
Under room temperature, the 0.5g silica dioxide granule that partial size is 5~70 nanometers is added in 20ml toluene, ultrasonic disperse After 15min, 0.5g trichlorine octadecylsilane is added dropwise in above-mentioned dispersion in whipping process, continues to stir 6h.Instead After answering, centrifugal treating removes supernatant.Ethanol washing product is to remove unreacted trichlorine octadecylsilane, at centrifugation It manages, alkylation silica dioxide granule is obtained after dry at 70 DEG C.
It is alkylated the preparation of silicon dioxide-poly tetrafluoro wax toluene solution
0.1g is alkylated the Polytetrafluoroethylene emulsion particle that silica dioxide granule and 0.05g partial size are 5~15 microns, 20ml is added In toluene, magnetic agitation 1h makes to be alkylated silica under room temperature and Polytetrafluoroethylene emulsion is uniformly dispersed in toluene, is alkylated Silicon dioxide-poly tetrafluoro wax toluene solution;
The preparation of superhydrophobic fabric
Cotton fibre fabric is immersed in 10min in alkylation silicon dioxide-poly tetrafluoro wax toluene solution, by cotton fibre fabric from upper It states in solution and takes out, 30min is dried at 130 DEG C to remove toluene, obtains super-hydrophobic cotton fibre fabric.
The contact angle for obtaining superhydrophobic fabric and water droplet is 157.7 o, roll angle 5.5 o.It is touched through finger, blade is drawn Cut and with (pressure at right angle 7N, frictional distance 30cm, friction velocity 3cm/s), the contact angle with water droplet after 30 opposite grindings of sand paper It is 151o, roll angle 15 o.When superhydrophobic fabric is immersed in dimeticone, contact angle of the water droplet on its surface is 162 o

Claims (5)

1. the preparation method with ultra-hydrophobicity fabric in a kind of air and oil, it is characterised in that include the following steps:
A is alkylated the preparation of silica,
Under room temperature, organochlorosilane is added dropwise into the toluene solution uniformly containing silica dioxide granule, then magnetic agitation 6h;
To after reaction, centrifugal treating simultaneously removes supernatant, unreacted organochlorine then is removed using ethanol washing product Silane, again centrifugal treating obtain alkylation silica dioxide granule after desciccate at 70 DEG C;
The mass ratio of silica used, organochlorosilane and toluene is 1:0.5 ~ 1:35 in the step;
Organochlorosilane used is any one in trichlorine octadecylsilane or trim,ethylchlorosilane in the step;
The partial size of silica used is 5~70 nanometers in the step;
B is alkylated the preparation of silicon dioxide-poly tetrafluoro wax toluene solution,
Silica dioxide granule will be alkylated and Polytetrafluoroethylene emulsion particle is added in toluene, magnetic agitation 1h makes to be alkylated dioxy under room temperature SiClx and Polytetrafluoroethylene emulsion are uniformly dispersed in toluene, obtain alkylation silicon dioxide-poly tetrafluoro wax toluene solution;
Alkylation silica used in the step, Polytetrafluoroethylene emulsion and toluene mass ratio be 4~1.5:1:85;
The partial size of Polytetrafluoroethylene emulsion used is 5~15 microns in the step;
The preparation of C superhydrophobic fabric,
It soaks the fabric into alkylation silicon dioxide-poly tetrafluoro wax toluene solution and is taken out after 1 ~ 30min, then 108 ~ 150 After drying removes toluene at DEG C, the fabric that ultra-hydrophobicity is all had in air and in oil is obtained.
2. the preparation method with ultra-hydrophobicity fabric in a kind of air according to claim 1 and oil, feature exist In the drying temperature of step C is 130 DEG C.
3. the preparation method with ultra-hydrophobicity fabric in a kind of air according to claim 1 or 2 and oil, feature It is, any one in dacron fabric or cotton fibre fabric of the fabric used selected from commercialization.
4. the preparation method with ultra-hydrophobicity fabric obtains in air and oily in a kind of air as claimed in claim 3 and oil In with ultra-hydrophobicity fabric.
5. the fabric with ultra-hydrophobicity is applied in water or in oil in air as claimed in claim 4 and oil.
CN201610525568.4A 2016-07-06 2016-07-06 Fabric and preparation method and purposes in a kind of air and oil with ultra-hydrophobicity Active CN106120339B (en)

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Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1824884A (en) * 2005-02-25 2006-08-30 中科纳米技术工程中心有限公司 Self-cleaning suiting containing nano-functional material and method for making garment products
CN102119197A (en) * 2008-06-30 2011-07-06 Stc.Unm公司 A superhydrophobic aerogel that does not require per-fluoro compounds or contain any fluorine
CN101481081B (en) * 2009-01-21 2011-07-06 重庆大学 Preparation of composite structure super-hydrophobic film
CN101481590B (en) * 2009-01-21 2012-07-04 重庆大学 Super-hydrophobic adhesive film
CN101768856B (en) * 2009-12-29 2011-12-28 陕西科技大学 Super hydrophobic cotton fabric and preparation method thereof
CN102995411B (en) * 2012-08-21 2014-12-10 江苏宝泽高分子材料股份有限公司 Yangbuck and cajiao treating agent for synthetic leather and preparation method thereof
US9056987B2 (en) * 2013-01-30 2015-06-16 Illinois Tool Works, Inc. Super hydrophobic coating
CN103467829B (en) * 2013-09-25 2015-10-28 南京天诗新材料科技有限公司 Wax aqueous dispersion of loaded with nano silicon-dioxide and its production and use
CN104403453B (en) * 2014-11-16 2017-01-18 重庆大学 Semiconductor superhydrophobic paint and preparation method thereof

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