CN106139924B - A kind of composite nanometer filtering film and preparation method thereof and the application in water treatment field - Google Patents
A kind of composite nanometer filtering film and preparation method thereof and the application in water treatment field Download PDFInfo
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Abstract
The invention discloses a kind of composite nanometer filtering films and preparation method thereof, and the application by the composite nanometer filtering film and the composite nanometer filtering film being prepared by the preparation method in water treatment field.The composite nanometer filtering film includes the supporting layer to stack together and separating layer, wherein, the separating layer is the initial composite NF membrane for the cross-linked structure that silane coupling agent of the hydroxy-end capped dimethyl silicone polymer with ethyl orthosilicate and containing sulfydryl is formed after heat cross-linking reacts in the support layer surface, then the initial composite NF membrane is post-processed in hydrogen peroxide.The present invention can will utilize hydrogen peroxide at sulfonic group, to obtain hydrophilic composite nanometer filtering film, further improve the water flux and salt rejection rate of the composite nanometer filtering film sulfhydryl oxidase by the way that initial composite NF membrane is carried out post-processing modification with hydrogen peroxide.
Description
Technical field
The present invention relates to a kind of composite nanometer filtering film and preparation method thereof, a kind of composite nanometer filter being prepared by this method
The application of film and the composite nanometer filtering film in water treatment field.
Background technology
Nanofiltration is a kind of pressure-driven membrane separating process between reverse osmosis between ultrafiltration, and the pore diameter range of NF membrane exists
Several rans, it is poor less than the removing of 200 organic matter to monovalention and molecular weight, and to divalent or multivalent ion and molecule
The organic matter measured between 200~500 has higher removal efficiency.It can be widely used in fresh water softening, seawater softening, drinking water
The chemical industry system such as purification, water correction, water-oil separating, wastewater treatment and recycling and dyestuff, antibiotic, polypeptide and polysaccharide
The fields such as classification, purifying and the concentration of product.
Membrane material is the core of membrane technology.The composite nanometer filtering film being commercialized, separation layer materials are that fragrance is poly- mostly
Amide.Aromatic polyamides have the advantages that salt rejection rate height, good water permeability, chemical stability are excellent and operating pressure is low etc..It is lacked
Point is that resistance to oxidation, ant-scaling and pollution capacity be not poor, and chlorine resistance is poor.New function polymer material is developed, is reinforced to UF membrane
Layer is ultra-thin and activating technology research, preparation resistance to oxidation, resistance to free chlorine and resistant to pollution NF membrane have a very important significance.
Dimethyl silicone polymer is widely used in preparing due to good film forming after its hydrophobic characteristic, and crosslinking
Gas separation membrane material.In addition, there is the dimethyl silicone polymer after crosslinking good solvent resistance, Linder to utilize it as
Separating layer is prepared for composite nanometer filter membrane material, for the polysaccharide and organic matter in Separation of Organic.It is hydrophobic due to material
Property, related dimethyl silicone polymer has not been reported as nanofiltration or reverse osmosis membrane materials applied to water treatment field.
Therefore, how to be separating layer to prepare composite nanometer filtering film by hydroxy-end capped dimethyl silicone polymer, and this is received
Filter membrane needs further R and D applied to water treatment field.
Invention content
It is an object of the invention to provide a kind of NEW TYPE OF COMPOSITE NF membranes and preparation method thereof, and be prepared by this method
Application of the composite nanometer filtering film in water treatment field.
To achieve the goals above, the present invention provides a kind of composite nanometer filtering film, and the composite nanometer filtering film includes being stacked in one
The supporting layer and separating layer risen, wherein the separating layer be hydroxy-end capped dimethyl silicone polymer and ethyl orthosilicate and
Silane coupling agent containing sulfydryl forms the initial multiple of the cross-linked structure in the support layer surface after heat cross-linking reacts
NF membrane is closed, then the initial composite NF membrane is post-processed in hydrogen peroxide.
The present invention also provides a kind of preparation methods of composite nanometer filtering film, and this approach includes the following steps：
(1) by hydroxy-end capped dimethyl silicone polymer, ethyl orthosilicate, the silane coupling agent containing sulfydryl and crosslinking
Catalyst, which is dissolved in solvent, is prepared into coating liquid；
(2) coating liquid is coated on supporting layer and is carried out heat cross-linking reaction, obtain including supporting layer and positioned at institute
State the initial composite film of the cross-linked structure in support layer surface；
(3) the initial composite NF membrane is post-processed in hydrogen peroxide, obtains modified composite nanometer filtering film.
The present invention also provides the composite nanometer filtering films being prepared by the above method.
The composite nanometer filtering film being prepared the present invention also provides above-mentioned composite nanometer filtering film and by the above method is in water process
Application in field.
The present inventor is by further investigation discovery, the hydroxy-end capped dimethyl silicone polymer and positive silicic acid
Ethyl ester and silane coupling agent containing sulfydryl form cross-linked structure after being reacted in the presence of a crosslinking catalyst by heat cross-linking,
Then, obtained initial composite NF membrane is further impregnated after a certain period of time in the hydrogen peroxide of specific temperature, is modified
Composite nanometer filtering film afterwards, not only increases the water penetration of film, and also increases the retention to inorganic salts and organic molecule
Performance.In conclusion separating layer of the present invention be by containing hydroxy-end capped dimethyl silicone polymer, ethyl orthosilicate with
Silane coupling agent containing sulfydryl is reacted by heat cross-linking and is formed after being post-processed with hydrogen peroxide；It is of the present invention multiple
Closing NF membrane not only has higher salt rejection rate and water penetration (water flux), can also be applied in water treatment field, Er Qieqi
Preparation method is simple, great prospects for commercial application.
Other features and advantages of the present invention will be described in detail in subsequent specific embodiment part.
Description of the drawings
Attached drawing is to be used to provide further understanding of the present invention, an and part for constitution instruction, with following tool
Body embodiment is used to explain the present invention together, but is not construed as limiting the invention.In the accompanying drawings：
Fig. 1 is the forming process schematic diagram of the separating layer of the composite nanometer filtering film prepared by the present invention.
Specific implementation mode
The specific implementation mode of the present invention is described in detail below.It should be understood that described herein specific
Embodiment is merely to illustrate and explain the present invention, and is not intended to restrict the invention.
The present invention provides a kind of composite nanometer filtering film, the composite nanometer filtering film includes the supporting layer to stack together and separation
Layer, wherein the separating layer is that silane of the hydroxy-end capped dimethyl silicone polymer with ethyl orthosilicate and containing sulfydryl is even
Connection agent forms the initial composite NF membrane of the cross-linked structure in the support layer surface after heat cross-linking reacts, then will be described
Initial composite NF membrane is post-processed in hydrogen peroxide.
According to the present invention, the viscosity in the hydroxy-end capped dimethyl silicone polymer can be 1000cSt-
100000cSt, preferably 5000cSt-50000cSt.
According to the present invention, the silane coupling agent containing sulfydryl can be γ mercaptopropyitrimethoxy silane and/or
γ-Mercaptopropyltriethoxysilane.
According to the present invention, the thickness of the supporting layer and separating layer is not particularly limited, and can be the routine of this field
Selection, but in order to enable this two layers can play the role of better coordinated, so as to get composite nanometer filtering film can be preferably
Have both higher water flux and salt rejection rate, under preferable case, the thickness of the supporting layer is 90-150 microns, the separating layer
Thickness is 0.1-0.5 microns；In the case of more preferably, the thickness of the supporting layer is 100-120 microns, the thickness of the separating layer
It is 0.2-0.4 microns；Under most preferred case, the thickness of the supporting layer is 105-115 microns, and the thickness of the separating layer is
0.2-0.3 microns.
According to the present invention, the supporting layer is not particularly limited, can be by existing various with certain intensity and energy
Be enough in nanofiltration, the material of reverse osmosis membrane is made, usually can be by polyacrylonitrile, Kynoar, the non-sulfonated poly- virtue of phenolphthalein type
One or more in ether sulfone, polyether sulfone and bisphenol-a polysulfone are made, and can know to this those skilled in the art, herein will
It repeats no more.
According to the present invention, in the forming process of the separating layer, with the hydroxy-end capped poly- diformazan of 100 parts by weight
On the basis of radical siloxane, the content of the ethyl orthosilicate can be 1-500 parts by weight, preferably 5-200 parts by weight, described to contain
It can be 0.5-200 parts by weight, preferably 1-100 parts by weight to have the content of the silane coupling agent of sulfydryl.
The present invention also provides a kind of preparation methods of composite nanometer filtering film, and this approach includes the following steps：
(1) by hydroxy-end capped dimethyl silicone polymer, ethyl orthosilicate, the silane coupling agent containing sulfydryl and crosslinking
Catalyst, which is dissolved in solvent, is prepared into coating liquid；
(2) coating liquid is coated on supporting layer and is carried out heat cross-linking reaction, obtain including supporting layer and positioned at institute
State the initial composite film of the cross-linked structure in support layer surface；
(3) the initial composite NF membrane is post-processed in hydrogen peroxide, obtains modified composite nanometer filtering film.
According to the present invention, the present invention is to hydroxy-end capped dimethyl silicone polymer, the ethyl orthosilicate in the coating liquid
Be not particularly limited with the dosage of the silane coupling agent containing sulfydryl, if the NF membrane enabled to can have both it is higher
Water flux and salt rejection rate, it is described hydroxy-end capped on the basis of the solvent of 100 parts by weight for example, in step (1)
The dosage of dimethyl silicone polymer can be 0.1-50 parts by weight, preferably 0.25-25 parts by weight；The use of the ethyl orthosilicate
Amount can be 0.002-10 parts by weight, preferably 0.01-5 parts by weight；The dosage of the silane coupling agent containing sulfydryl can be with
For 0.001-5 parts by weight, preferably 0.005-2.5 parts by weight.
According to the present invention, the present invention by hydroxy-end capped dimethyl silicone polymer, ethyl orthosilicate, contain the silicon of sulfydryl
During alkane coupling agent and crosslinking catalyst are dissolved in solvent, preferably carry out under stirring conditions, the present invention is to described
The condition of stirring and the equipment of stirring are not particularly limited, and the conventional stirring that can be well known to those skilled in the art is set
It is standby to be carried out under stirring condition appropriate, as long as hydroxy-end capped dimethyl silicone polymer can be made, ethyl orthosilicate, contain mercapto
The silane coupling agent and crosslinking catalyst of base are completely dissolved in solvent.In addition, the present invention gathers by hydroxy-end capped
The process that dimethyl siloxane, ethyl orthosilicate, the silane coupling agent containing sulfydryl and crosslinking catalyst are dissolved in solvent exists
It is carried out under room temperature.
According to the present invention, the present invention is not particularly limited the thickness of the supporting layer, can be the routine of this field
Selection, but in order to enable the supporting layer and the separating layer can play the role of better coordinated, make it is compound
NF membrane can preferably have both higher water flux and salt rejection rate, and under preferable case, the thickness of the supporting layer is 90-150
Micron, preferably 100-120 microns.
According to the present invention, the present invention is not particularly limited the dosage of the coating liquid, but in order to enable the nanofiltration arrived
Film can preferably have both higher water flux and salt rejection rate, and under preferable case, the dosage of the coating liquid makes the separation
The thickness of layer is 0.1-0.5 microns, preferably 0.2-0.4 microns.
According to the present invention, during the coating liquid is coated in supporting layer, to the method for the coating in this hair
It is bright to be not particularly limited, in the spraying that can be well known to those skilled in the art, blade coating, spin coating etc. any one.
According to the present invention, after coating liquid is coated uniformly on supporting layer, under preferable case, this is coated with coating liquid
Supporting layer to be put into baking oven complete solvent therein to volatilize, do not have to its temperature and time in an oven in the present invention
Body limits, as long as can ensure that solvent volatilization is complete, under preferable case, and the dry 20- in the baking oven that temperature is 50-70 DEG C
It is 40 minutes, 25-35 minutes dry in the baking oven that temperature is 55-65 DEG C in the case of more preferable.
According to the present invention, the present invention is not particularly limited the type of the solvent, as long as the hydroxyl can be dissolved
Dimethyl silicone polymer, ethyl orthosilicate, the silane coupling agent and crosslinking catalyst containing sulfydryl of sealing end, for example,
In step (1), the solvent can be n-hexane, normal heptane, petroleum ether and isoparaffin solvent oil in it is one or more,
Preferably isoparaffin solvent oil；Wherein, the isoparaffin solvent oil can be alkane solvent oil ISOPA E, alkane solvent
It is one or more in oily ISOPA G and alkane solvent oil ISOPA H, preferably alkane solvent oil ISOPA E or alkane solvent
Oily ISOPA G.
According to the present invention, in step (2), the condition of the heat cross-linking reaction may include：The item of the cross-linking reaction
Part includes：Crosslinking temperature is 50-150 DEG C, and crosslinking time is 1-24 hours；Preferably, crosslinking temperature is 60-120 DEG C, when crosslinking
Between be 2-10 hours.
According to the present invention, the present invention is not particularly limited the dosage of the crosslinking catalyst in the crosslinker solution, only
The composite nanometer filtering film enabled to can have both higher water flux and salt rejection rate.In the present invention, used
Crosslinking catalyst can be dibutyl tin laurate；And with the hydroxy-end capped dimethyl silicone polymer of 100 parts by weight
On the basis of, the dosage of the dibutyl tin laurate can be 0.01-10 parts by weight, preferably 0.05-5 parts by weight.
According to the present invention, in step (3), the initial composite NF membrane is post-processed with hydrogen peroxide, is changed
Composite nanometer filtering film after property.Wherein, the condition of the post-processing may include：Post-processing temperature is 25-100 DEG C, when post-processing
Between be -10 hours 1 minute；Preferably, post-processing temperature is 40-80 DEG C, and finishing time is -5 hours 10 minutes.In the condition
Under carry out post-processing modification, the composite nanometer filtering film enabled to can have both higher water flux and salt rejection rate.
According to the present invention, the mass concentration of the hydrogen peroxide can be 0.1-20 weight %, preferably 1-10 weight %.
Post-processing modification is carried out under this condition, and the composite nanometer filtering film enabled to can have both higher water flux and salt rejection rate.
In short, initial composite NF membrane is carried out post-processing modification by the present invention by hydrogen peroxide, it can utilize hydrogen peroxide will
Sulfhydryl oxidase obtains hydrophilic composite nanometer filtering film at sulfonic group, further improves water flux and the desalination of the composite nanometer filtering film
Rate.According to the present invention, since the hydroxy-end capped dimethyl silicone polymer has higher molecular weight, in a solvent very
Difficulty is completely dissolved, therefore, in order to enable to cross-linked structure be more uniformly distributed, and improve the composite nanometer filtering film performance stablize
Property, under preferable case, the preparation method of the composite nanometer filtering film further includes that will the coating liquid be coated on supporting layer it
Before, the coating liquid is filtered.In specific operation process, can first by the hydroxy-end capped dimethyl silicone polymer, just
Silester and silane coupling agent containing sulfydryl are dissolved in solvent and filter, and obtain the coating liquid of homogeneous transparent；In addition, for
The filtering is also not particularly limited, the filter method and equipment that can be well known to those skilled in the art.
According to the present invention, in order to enable the composite nanometer filtering film arrived is more smooth, it is preferable that composite nanometer filter provided by the invention
The preparation method of film further includes that the supporting layer is fixed on a glass or applied before coating liquid is coated on supporting layer
On film machine.
The present invention also provides the composite nanometer filtering films being prepared by preparation method provided by the present invention.
The present invention also provides by composite nanometer filtering film of the present invention and by the preparation method system of the present invention
Application of the standby composite nanometer filtering film in water treatment field.
The present invention will be described in detail by way of examples below.
In the following Examples and Comparative Examples：
(1) water flux of composite nanometer filtering film is tested obtain by the following method：Composite nanometer filter permeable membrane is fitted into membrane cisterna,
Under 1.2MPa after precompressed 0.5 hour, under pressure is 2.0MPa, temperature be 25 DEG C under the conditions of measure the water of the NF membrane in 1h
Transit dose, and be calculated by the following formula to obtain：
J=Q/ (At), wherein J is water flux, and Q is water transit dose (L), and A is effective membrane area of composite nanometer filtering film
(m2), t is the time (h)；
(2) salt rejection rate of composite nanometer filtering film tests obtain by the following method：Composite nanometer filtering film is fitted into membrane cisterna,
Under 1.2MPa after precompressed 0.5h, under pressure is 2.0MPa, temperature be 25 DEG C under the conditions of to measure initial concentration in 1h be 2000ppm
Sodium sulphate raw water solution and permeate in the concentration of sodium sulphate change, and be calculated by the following formula to obtain：
R=(Cp-Cf)/Cp× 100%, wherein R is salt rejection rate, CpFor the concentration of sodium sulphate in stoste, CfFor in permeate
The concentration of sodium sulphate；
(3) composite nanometer filtering film includes the supporting layer to stack together and separating layer, wherein the thickness of supporting layer and separating layer
It can be obtained by scanning electron microscope observation.
In addition, in the following Examples and Comparative Examples：
Hydroxy-end capped dimethyl silicone polymer (viscosity 2000cSt-50000cSt), γ-mercaptopropyi triethoxysilicane
Alkane, γ mercaptopropyitrimethoxy silane are purchased from lark prestige Science and Technology Ltd.；Polysulfones counterdie is purchased from the beautiful easily film science and technology in Hangzhou
Co., Ltd, thickness are 120 microns；Hydrogen peroxide, alkane solvent oil ISOPA E, alkane solvent oil ISOPA G, ethyl orthosilicate
And dibutyl tin laurate etc. is purchased from Sinopharm Chemical Reagent Co., Ltd.；
Scanning electron microscope (SEM) is purchased from Hitachi, Japan model S-4800.
Embodiment 1
The embodiment is for illustrating composite nanometer filtering film provided by the invention and preparation method thereof.
By dimethyl silicone polymer (viscosity 20000cSt) hydroxy-end capped 1.0g, 0.1g ethyl orthosilicates, 0.2g γ-
Mercaptopropyltriethoxysilane and 0.03g dibutyl tin laurates are dissolved in 100g solvent naphtha ISOPA E.In room temperature
Under, after stirring 2h, clarification coating liquid is obtained by filtration；
After coating weak solution is uniformly coated on polysulfones counterdie, it is then placed in 50 DEG C of baking oven and heats 10min, really
It is complete to protect solvent volatilization, then heats to 75 DEG C, being maintained at temperature 4h ensures that crosslinking is complete；
Obtained initial composite NF membrane is immersed in the aqueous solution containing 4 weight % hydrogen peroxide, under the conditions of 60 DEG C
Modified composite nanometer filtering film is obtained after heating 1h, which is taken out, is rinsed well with deionized water, is immersed in
In ionized water；
After obtained composite nanometer filtering film is impregnated 24 hours in water, then pressure is 2.0MPa, temperature is 25 DEG C of items
Water flux and salt rejection rate are measured under part, the results are shown in Table 1；
Obtained composite nanometer filtering film includes the supporting layer to stack together and separating layer, wherein the thickness of supporting layer is 110
The thickness of micron, separating layer is 0.22 micron.
Fig. 1 gives the formation mechenism of the separating layer of composite nanometer filtering film prepared by method using the present invention.First, hydroxyl
The dimethyl silicone polymer of sealing end and ethyl orthosilicate and γ-Mercaptopropyltriethoxysilane, under the effect of the catalyst
Reaction forms cross-linked structure；Then, using hydrogen peroxide by sulfhydryl oxidase at sulfonic group, obtain hydrophilic composite nanometer filtering film.
Embodiment 2
By dimethyl silicone polymer (viscosity 3500cSt) hydroxy-end capped 1.2g, 0.15g ethyl orthosilicates, 0.15g
γ mercaptopropyitrimethoxy silane and 0.02g dibutyl tin laurates are dissolved in 100g solvent naphtha ISOPA E.Normal
Under temperature, after stirring 2h, clarification coating liquid is obtained by filtration；
After coating weak solution is uniformly coated on polysulfones counterdie, it is then placed in 50 DEG C of baking oven and heats 10min, really
It is complete to protect solvent volatilization, then heats to 75 DEG C, being maintained at temperature 4h ensures that crosslinking is complete；
Obtained initial composite NF membrane is immersed in the aqueous solution containing 4% hydrogen peroxide, is heated under the conditions of 60 DEG C
Modified composite nanometer filtering film is obtained after 1h, which is taken out, is rinsed well with deionized water, deionization is immersed in
In water；
After obtained composite nanometer filtering film is impregnated 24 hours in water, then pressure is 2.0MPa, temperature is 25 DEG C of items
Water flux and salt rejection rate are measured under part, the results are shown in Table 1；
Obtained composite nanometer filtering film includes the supporting layer to stack together and separating layer, wherein the thickness of supporting layer is 112
The thickness of micron, separating layer is 0.20 micron.
Embodiment 3
By dimethyl silicone polymer (viscosity 50000cSt) hydroxy-end capped 0.8g, 0.05g ethyl orthosilicates, 0.1g
γ-Mercaptopropyltriethoxysilane and 0.01g dibutyl tin laurates are dissolved in 100g solvent naphtha ISOPA E.Normal
Under temperature, after stirring 2h, clarification coating liquid is obtained by filtration；
After coating weak solution is uniformly coated on polysulfones counterdie, it is then placed in 50 DEG C of baking oven and heats 10min, really
It is complete to protect solvent volatilization, then heats to 75 DEG C, being maintained at temperature 4h ensures that crosslinking is complete；
Obtained initial composite NF membrane is immersed in the aqueous solution containing 4% hydrogen peroxide, is heated under the conditions of 60 DEG C
Modified composite nanometer filtering film is obtained after 1h, which is taken out, is rinsed well with deionized water, deionization is immersed in
In water.
After obtained composite nanometer filtering film is impregnated 24 hours in water, then pressure is 2.0MPa, temperature is 25 DEG C of items
Water flux and salt rejection rate are measured under part, the results are shown in Table 1；
Obtained composite nanometer filtering film includes the supporting layer to stack together and separating layer, wherein the thickness of supporting layer is 110
The thickness of micron, separating layer is 0.27 micron.
Embodiment 4
According to prepare the preparation method of composite nanometer filtering film identical with implementing 1, institute the difference is that, initial answered what is obtained
NF membrane is closed to be immersed in the aqueous solution containing 3 weight % hydrogen peroxide；
After obtained composite nanometer filtering film is impregnated 24 hours in water, then pressure is 2.0MPa, temperature is 25 DEG C of items
Water flux and salt rejection rate are measured under part, the results are shown in Table 1；
Obtained composite nanometer filtering film includes the supporting layer to stack together and separating layer, wherein the thickness of supporting layer is 114
The thickness of micron, separating layer is 0.22 micron.
Embodiment 5
According to prepare the preparation method of composite nanometer filtering film identical with implementing 1, institute the difference is that, initial answered what is obtained
NF membrane is closed to be immersed in the aqueous solution containing 5 weight % hydrogen peroxide；
After obtained composite nanometer filtering film is impregnated 24 hours in water, then pressure is 2.0MPa, temperature is 25 DEG C of items
Water flux and salt rejection rate are measured under part, the results are shown in Table 1；
Obtained composite nanometer filtering film includes the supporting layer to stack together and separating layer, wherein the thickness of supporting layer is 110
The thickness of micron, separating layer is 0.22 micron.
Embodiment 6
According to prepare the preparation method of composite nanometer filtering film identical with implementing 1, institute the difference is that, initial answered what is obtained
NF membrane is closed to be immersed in the aqueous solution containing 4 weight % hydrogen peroxide；Modified answer is obtained after heating 1h under the conditions of 50 DEG C
Close NF membrane；
After obtained composite nanometer filtering film is impregnated 24 hours in water, then pressure is 2.0MPa, temperature is 25 DEG C of items
Water flux and salt rejection rate are measured under part, the results are shown in Table 1；
Obtained composite nanometer filtering film includes the supporting layer to stack together and separating layer, wherein the thickness of supporting layer is 112
The thickness of micron, separating layer is 0.21 micron.
Embodiment 7
According to prepare the preparation method of composite nanometer filtering film identical with implementing 1, institute the difference is that, initial answered what is obtained
NF membrane is closed to be immersed in the aqueous solution containing 4 weight % hydrogen peroxide；Modified answer is obtained after heating 1h under the conditions of 70 DEG C
Close NF membrane；
After obtained composite nanometer filtering film is impregnated 24 hours in water, then pressure is 2.0MPa, temperature is 25 DEG C of items
Water flux and salt rejection rate are measured under part, the results are shown in Table 1；
Obtained composite nanometer filtering film includes the supporting layer to stack together and separating layer, wherein the thickness of supporting layer is 110
The thickness of micron, separating layer is 0.22 micron.
Embodiment 8
According to prepare the preparation method of composite nanometer filtering film identical with implementing 1, institute the difference is that, initial answered what is obtained
Close NF membrane be immersed in the aqueous solution containing 4 weight % hydrogen peroxide, under the conditions of 60 DEG C heat 0.5h after obtain it is modified
Composite nanometer filtering film；
After obtained composite nanometer filtering film is impregnated 24 hours in water, then pressure is 2.0MPa, temperature is 25 DEG C of items
Water flux and salt rejection rate are measured under part, the results are shown in Table 1；
Obtained composite nanometer filtering film includes the supporting layer to stack together and separating layer, wherein the thickness of supporting layer is 112
The thickness of micron, separating layer is 0.23 micron.
Embodiment 9
According to prepare the preparation method of composite nanometer filtering film identical with implementing 1, institute the difference is that, initial answered what is obtained
NF membrane is closed to be immersed in the aqueous solution containing 4 weight % hydrogen peroxide；Modified answer is obtained after heating 2h under the conditions of 60 DEG C
Close NF membrane；
After obtained composite nanometer filtering film is impregnated 24 hours in water, then pressure is 2.0MPa, temperature is 25 DEG C of items
Water flux and salt rejection rate are measured under part, the results are shown in Table 1；
Obtained composite nanometer filtering film includes the supporting layer to stack together and separating layer, wherein the thickness of supporting layer is 110
The thickness of micron, separating layer is 0.22 micron.
Comparative example 1
According to prepare the preparation method of composite nanometer filtering film identical with implementing 1, institute the difference is that, obtained composite membrane is not
It is modified post-processing through hydrogen peroxide.The results are shown in Table 1 for its water flux and salt rejection rate；
Obtained composite nanometer filtering film includes the supporting layer to stack together and separating layer, wherein the thickness of supporting layer is 110
The thickness of micron, separating layer is 0.23 micron.
Table 1
| Embodiment | Water flux (L/m2h) | Salt rejection rate (%) |
| Embodiment 1 | 31.1 | 90.36 |
| Embodiment 2 | 25.7 | 91.09 |
| Embodiment 3 | 22.1 | 88.52 |
| Embodiment 4 | 20.6 | 89.25 |
| Embodiment 5 | 45.8 | 85.00 |
| Embodiment 6 | 23.4 | 90.20 |
| Embodiment 7 | 55.1 | 85.10 |
| Embodiment 8 | 28.6 | 90.15 |
| Embodiment 9 | 40.2 | 82.37 |
| Comparative example 1 | 8.3 | 81.73 |
From above example 1-9 impregnate in water 24 hours after result can be seen that composite nanometer filter provided by the invention
Film has excellent water flux and salt-stopping rate, and preparation method provided by the invention is simple, great prospects for commercial application.Into one
Step, can be seen that from the comparing result of embodiment 1-9 and comparative example 1 and carries out initial composite NF membrane without with hydrogen peroxide
Water flux and the salt-stopping rate for post-processing modified composite nanometer filtering film are relatively low, can reduce the application efficiency of the composite nanometer filtering film in this way,
Waste of energy largely limits the commercial Application of this composite nanometer filtering film.
In addition, Fig. 1 is the forming process schematic diagram of the separating layer of the composite nanometer filtering film prepared by the present invention, it can be with by Fig. 1
Find out, the present invention can will utilize hydrogen peroxide by sulfydryl by the way that initial composite NF membrane is carried out post-processing modification with hydrogen peroxide
It is oxidized to sulfonic group, obtains hydrophilic composite nanometer filtering film, further improves the water flux and salt rejection rate of the composite nanometer filtering film.
The preferred embodiment of the present invention has been described above in detail, still, during present invention is not limited to the embodiments described above
Detail can carry out a variety of simple variants to technical scheme of the present invention within the scope of the technical concept of the present invention, this
A little simple variants all belong to the scope of protection of the present invention.
It is further to note that specific technical features described in the above specific embodiments, in not lance
In the case of shield, can be combined by any suitable means, in order to avoid unnecessary repetition, the present invention to it is various can
The combination of energy no longer separately illustrates.
In addition, various embodiments of the present invention can be combined randomly, as long as it is without prejudice to originally
The thought of invention, it should also be regarded as the disclosure of the present invention.
Claims (23)
1. a kind of composite nanometer filtering film, the composite nanometer filtering film includes the supporting layer to stack together and separating layer, which is characterized in that
The separating layer is silane coupling agent of the hydroxy-end capped dimethyl silicone polymer with ethyl orthosilicate and containing sulfydryl through heat
The initial composite NF membrane for the cross-linked structure being located in the support layer surface is formed after cross-linking reaction, then by the initial composite
What NF membrane was post-processed in hydrogen peroxide.
2. composite nanometer filtering film according to claim 1, wherein the thickness of the supporting layer is 90-150 microns；Described point
The thickness of absciss layer is 0.1-0.5 microns.
3. composite nanometer filtering film according to claim 2, wherein the thickness of the supporting layer is 100-120 microns；Described point
The thickness of absciss layer is 0.2-0.4 microns.
4. composite nanometer filtering film according to claim 1, wherein with the hydroxy-end capped poly dimethyl of 100 parts by weight
On the basis of siloxanes, the content of the ethyl orthosilicate is 1-500 parts by weight, the content of the silane coupling agent containing sulfydryl
For 0.5-200 parts by weight.
5. composite nanometer filtering film according to claim 4, wherein with the hydroxy-end capped poly dimethyl of 100 parts by weight
On the basis of siloxanes, the content of the ethyl orthosilicate is 5-200 parts by weight, the content of the silane coupling agent containing sulfydryl
For 1-100 parts by weight.
6. composite nanometer filtering film according to claim 1 or 5, wherein the hydroxy-end capped dimethyl silicone polymer glues
Degree is 1000cSt-100000cSt.
7. composite nanometer filtering film according to claim 6, wherein the viscosity of the hydroxy-end capped dimethyl silicone polymer is
2000cSt-50000cSt。
8. composite nanometer filtering film according to claim 1 or 5, wherein the silane coupling agent containing sulfydryl is γ-sulfydryl
Propyl trimethoxy silicane and/or γ-Mercaptopropyltriethoxysilane.
9. the preparation method of the composite nanometer filtering film described in any one of claim 1-8, this approach includes the following steps：
(1) by hydroxy-end capped dimethyl silicone polymer, ethyl orthosilicate, silane coupling agent and cross-linking catalyst containing sulfydryl
Agent, which is dissolved in solvent, is prepared into coating liquid；
(2) coating liquid is coated on supporting layer and is carried out heat cross-linking reaction, obtain including supporting layer and positioned at the branch
Support the initial composite film of the cross-linked structure in layer surface；
(3) the initial composite NF membrane is post-processed in hydrogen peroxide, obtains modified composite nanometer filtering film.
10. preparation method according to claim 9, wherein in step (1), on the basis of the solvent of 100 parts by weight,
The dosage of the hydroxy-end capped dimethyl silicone polymer is 0.1-50 parts by weight；The dosage of the ethyl orthosilicate is 0.002-
10 parts by weight；The dosage of the silane coupling agent containing sulfydryl is 0.001-5 parts by weight.
11. preparation method according to claim 10, wherein described hydroxy-end capped on the basis of the solvent of 100 parts by weight
Dimethyl silicone polymer dosage be 0.25-25 parts by weight；The dosage of the ethyl orthosilicate is 0.01-5 parts by weight；It is described
The dosage of silane coupling agent containing sulfydryl is 0.005-2.5 parts by weight.
12. the preparation method according to claim 9 or 11, wherein in step (1), the solvent is n-hexane, positive heptan
It is one or more in alkane, petroleum ether and isoparaffin solvent oil.
13. preparation method according to claim 12, wherein the solvent is isoparaffin solvent oil.
14. preparation method according to claim 9, wherein in step (1), the crosslinking catalyst is tin dilaurate
Dibutyl tin, and on the basis of the hydroxy-end capped dimethyl silicone polymer of 100 parts by weight, the di lauric dibutyl
The dosage of tin is 0.01-10 parts by weight.
15. preparation method according to claim 14, wherein with the hydroxy-end capped poly dimethyl of 100 parts by weight
On the basis of siloxanes, the dosage of the dibutyl tin laurate is 0.05-5 parts by weight.
16. preparation method according to claim 9, wherein in step (2), the condition of the cross-linking reaction includes：It hands over
It is 50-150 DEG C to join temperature, and crosslinking time is 1-24 hours.
17. preparation method according to claim 16, wherein crosslinking temperature is 60-120 DEG C, and crosslinking time is that 2-10 is small
When.
18. preparation method according to claim 9, wherein in step (3), the condition of the post-processing includes：After
It is 25-100 DEG C to manage temperature, and finishing time is -10 hours 1 minute.
19. preparation method according to claim 18, wherein post-processing temperature is 40-80 DEG C, and finishing time is 10 points
Clock -5 hours.
20. preparation method according to claim 19, wherein with the mass concentration of the hydrogen peroxide be 0.1-20 weight
Measure %.
21. preparation method according to claim 20, wherein with the mass concentration of the hydrogen peroxide for 1-10 weight %.
22. the composite nanometer filtering film being prepared by the preparation method described in any one of claim 9-21.
23. by application of the composite nanometer filtering film described in claims 1 or 22 in water treatment field.
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| Publication number | Priority date | Publication date | Assignee | Title |
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| EP0346773A2 (en) * | 1988-06-13 | 1989-12-20 | Asahi Kasei Kogyo Kabushiki Kaisha | Selectively ion-adsorptive, porous membrane |
| CN103752183A (en) * | 2014-01-21 | 2014-04-30 | 清华大学 | Composite separation film and preparation method thereof |
| CN104258746A (en) * | 2014-09-03 | 2015-01-07 | 北京工商大学 | Preparation method of modified organosilicone dephenolized membrane |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0346773A2 (en) * | 1988-06-13 | 1989-12-20 | Asahi Kasei Kogyo Kabushiki Kaisha | Selectively ion-adsorptive, porous membrane |
| CN103752183A (en) * | 2014-01-21 | 2014-04-30 | 清华大学 | Composite separation film and preparation method thereof |
| CN104258746A (en) * | 2014-09-03 | 2015-01-07 | 北京工商大学 | Preparation method of modified organosilicone dephenolized membrane |
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