KR20190143238A - Composition for interfacial polymerizing polyamide and method for manufacturing water-treatment membrane using the same - Google Patents

Abstract

The present invention relates to a composition for polyamide interfacial polymerization comprising an amine compound, a pyrimidine-based compound and a purine-based compound. The present invention also relates to a method for producing a water treatment separation membrane using the same, and a water treatment separation membrane. According to the present invention, it is possible to enhance the salt removal rate.

Description

Composition for polyamide interfacial polymerization and method for preparing water treatment membrane using same {COMPOSITION FOR INTERFACIAL POLYMERIZING POLYAMIDE AND METHOD FOR MANUFACTURING WATER-TREATMENT MEMBRANE USING THE SAME}

The present specification relates to a composition for polyamide interfacial polymerization and a method for producing a water treatment membrane using the same.

Osmotic phenomenon in which a solvent moves from a solution having a low solute concentration toward a high solution between two solutions separated by a semipermeable membrane is called an osmotic phenomenon. Is called osmotic pressure. However, applying an external pressure higher than osmotic pressure causes the solvent to move toward a solution with a low concentration of solute. This phenomenon is called reverse osmosis. Using the reverse osmosis principle, a pressure gradient can be used as a driving force to separate various salts or organic substances through the semipermeable membrane. The water treatment membrane using the reverse osmosis phenomenon is used to separate the material of the molecular level, remove the salt from the brine or sea water to supply the domestic, construction, industrial water.

Representative examples of such water treatment membranes include polyamide-based water treatment membranes, and polyamide-based water treatment membranes are manufactured by forming a polyamide active layer on a microporous support, and more specifically, polysulfide on a nonwoven fabric. A phone layer is formed to form a microporous support, and the microporous support is immersed in an aqueous solution of m-phenylenediamine (mPD) to form an mPD layer, which in turn is trimesoyl chloride (TMC). A polyamide layer is prepared by immersing in an organic solvent to bring the mPD layer into contact with TMC and interfacial polymerization to form a polyamide layer.

The salt removal rate in the water treatment membrane is used as an important indicator of the membrane performance.

Korea Patent Publication No. 10-1999-0019008

The present specification is to provide a composition for polyamide interfacial polymerization and a method for producing a water treatment membrane using the same.

One embodiment of the present specification

Provided is a composition for polyamide interfacial polymerization comprising an amine compound, a pyrimidine compound and a purine compound.

In addition, an exemplary embodiment of the present specification

Preparing a porous support; And

It provides a method for producing a water treatment separation membrane comprising the step of interfacial polymerization of the polyamide interfacial polymerization composition and the acyl halide compound to form a polyamide active layer on the porous support.

In addition, an exemplary embodiment of the present specification

Porous support; And

A polyamide active layer provided on the porous support and including a pyrimidine compound and a purine compound

It provides a water treatment separation membrane comprising a.

In addition, an exemplary embodiment of the present specification provides a water treatment module including one or more of the water treatment separation membrane.

When the water treatment separation membrane is prepared using the polyamide interfacial polymerization composition according to the exemplary embodiment of the present specification, purine and pyrimidine base nitrogen are stably present through the binding, thereby improving salt removal rate.

1 illustrates a water treatment separation membrane according to an exemplary embodiment of the present specification.

Hereinafter, this specification is demonstrated in detail.

In one embodiment of the present specification, the polyamide interfacial polymerization composition includes an amine compound, a pyrimidine compound, and a purine compound.

When the polyamide active layer is prepared using the polyamide interfacial polymerization composition according to the present invention, the surface energy may be controlled during interfacial polymerization, and the main monomers of the terminal functional groups and interfacial polymerization of the purine-based compound and the pyrimidine-based compound may be used. Since the functional group of the phosphorus TMC forms a covalent bond, since the purine and pyrimidine base nitrogen are stably present, the performance of the water treatment membrane may be improved.

In particular, when the pyrimidine-based compound and the purine-based compound are used together, there is an advantage that the salt removal rate can be more stably secured compared to the case where the pyrimidine-based compound is used alone.

In the present specification, when a member is located 'on' another member, this includes not only when one member is in contact with another member but also when another member exists between the two members.

In the present specification, when a part is used to 'include' a certain component, this means that the component may further include other components, except for the case where there is no description to the contrary.

In the present specification, the alkyl group may be linear or branched, and the carbon number is not particularly limited, but is preferably 1 to 50. Specific examples include methyl, ethyl, propyl, n-propyl, isopropyl, butyl, n-butyl, isobutyl, tert-butyl, sec-butyl, 1-methylbutyl, 1-ethylbutyl, pentyl, n-pentyl, iso Pentyl, neopentyl, tert-pentyl, hexyl, n-hexyl, 1-methylpentyl, 2-methylpentyl, 4-methyl-2-pentyl, 3,3-dimethylbutyl, 2-ethylbutyl, heptyl, n-heptyl , 1-methylhexyl, cyclopentylmethyl, cyclohexylmethyl, octyl, n-octyl, tert-octyl, 1-methylheptyl, 2-ethylhexyl, 2-propylpentyl, n-nonyl, 2,2-dimethylheptyl, 1-ethyl-propyl, 1,1-dimethyl-propyl, isohexyl, 2-methylhexyl, 4-methylhexyl and 5-methylhexyl, and the like.

는 단일결합 또는 이중결합 중 선택될 수 있음을 의미한다.In the present specification,

Means that a single bond or double bond can be selected.

In one embodiment of the present specification, the pyrimidine-based compound may include at least one selected from a carbonyl group and a hydroxy group.

In one embodiment of the present specification, the pyrimidine-based compound may be represented by the following Formula 1.

[Formula 1]

In Chemical Formula 1,

X is N or NH,

Y is O or OH,

Z is O, OH or NH ₂ ,

R1 and R2 are each hydrogen; Or an alkyl group,

는 단일결합 또는 이중결합이다.

Is a single bond or a double bond.

In an exemplary embodiment of the present specification, when the pyrimidine-based compound includes a carbonyl group or a hydroxyl group, that is, when O or OH is substituted at the Y position of Chemical Formula 1, a hydrogen bond is induced to increase the flow rate. There is this.

In one embodiment of the present specification, the pyrimidine-based compound includes a carbonyl group.

In one embodiment of the present specification, the pyrimidine-based compound includes a hydroxy group.

In one embodiment of the present specification, X is N, Y is O, and Z is NH ₂ .

In one embodiment of the present specification, X is NH, Y is O, and Z is O.

In one embodiment of the present specification, R1 and R2 are each hydrogen; Or a linear alkyl group having 1 to 5 carbon atoms.

In one embodiment of the present specification, R1 is a methyl group, and R2 is hydrogen.

In one embodiment of the present specification, R1 and R2 are each hydrogen.

In one embodiment of the present specification, the pyrimidine-based compound may be represented by the following Chemical Formula 2-1 or 2-2.

[Formula 2-1]

[Formula 2-2]

In Chemical Formulas 2-1 and 2-2,

X, Z, R1 and R2 are the same as defined in the formula (1).

In one embodiment of the present specification, the pyrimidine-based compound may be represented by the following Chemical Formula 3-1 or 3-2.

[Formula 3-1]

[Formula 3-2]

In Chemical Formulas 3-1 and 3-1,

Z 'is OH or NH ₂ ,

R1 and R2 are each hydrogen; Or an alkyl group.

In one embodiment of the present specification, the pyrimidine-based compound is at least one selected from uracil, cytosine, and thymine.

In one embodiment of the present specification, the pyrimidine-based compound is uracil.

In one embodiment of the present specification, the pyrimidine-based compound may include a carbonyl group or a hydroxyl group as a tautomer according to pH.

In one embodiment of the present specification, the content of the pyrimidine-based compound is 0.001wt% to 1wt%, preferably 0.005wt% to 0.1wt%, more preferably based on 100wt% of the polyamide interfacial polymerization composition Is 0.05 wt% to 0.1 wt%.

When the pyrimidine-based compound is contained in an amount of 0.001wt% or more, the effect of increasing the salt removal rate due to the addition of the pyrimidine-based compound may be sufficiently exhibited. Excessive reduction can be prevented.

In one embodiment of the present specification, the purine-based compound is purine, adenine, guanine, hypoxanthine, xanthine, theobromine, caffeine, and caffeine. ), Uric acid and isoguanine.

In one embodiment of the present specification, the purine compound is guanine.

In one embodiment of the present specification, the pyrimidine-based compound is uracil, and the purine-based compound is guanine.

In one embodiment of the present specification, the pyrimidine compound is uracil, and the purine compound is xanthine.

In one embodiment of the present specification, the pyrimidine compound is cytosine, and the purine compound is guanine.

In one embodiment of the present specification, the pyrimidine compound is thymine and the purine compound is guanine.

In one embodiment of the present specification, the content of the purine-based compound is 0.001wt% to 1wt%, preferably 0.005wt% to 0.1wt%, more preferably based on 100wt% of the polyamide interfacial polymerization composition 0.005 wt% to 0.05 wt%.

If the content of the purine-based compound is 0.001wt% or more, the effect of increasing the salt removal rate due to the addition of the purine-based compound may be sufficiently exhibited. The phenomenon of decreasing can be prevented.

In one embodiment of the present specification, the content of the pyrimidine-based compound and pyrine-based compound is 0.01wt% to 0.2wt% based on 100wt% of the polyamide interfacial polymerization composition, preferably 0.015wt% to 0.15 wt%, more preferably 0.06 wt% to 0.11 wt%.

In one embodiment of the present specification, the amine compound is not limited as long as it can be used for the polymerization of polyamide, m-phenylenediamine (mPD), p-phenylenediamine (PPD), 1,3,6- Benzenetriamine (TAB), 4-chloro-1,3-phenylenediamine, 6-chloro-1,3-phenylenediamine, 3-chloro-1,4-phenylenediamine or mixtures thereof, Preferably m-phenylenediamine (mPD).

In one embodiment of the present specification, the content of the amine compound may be 0.1wt% to 20wt% based on 100wt% of the polyamide interfacial polymerization composition, preferably 1wt% to 15wt%, more preferably 3 wt% to 10 wt%.

Production of a uniform polyamide layer is possible when the content of the amine compound is in the above range.

In one embodiment of the present specification, the polyamide interfacial polymerization composition may further include a surfactant.

In the interfacial polymerization of the polyamide active layer, polyamide is rapidly formed at the interface between the aqueous solution layer and the organic solution layer. At this time, the surfactant makes the layer thin and uniform so that the amine compound present in the aqueous solution layer easily moves to the organic solution layer. Allow a uniform polyamide active layer to be formed.

In one embodiment of the present specification, the surfactant may be selected from nonionic, cationic, anionic and amphoteric surfactants. According to an exemplary embodiment of the present specification, the surfactant is sodium lauryl sulfate (SLS); Alkyl ether sulfates; Alkyl sulfates; Olefin sulfonates; Alkyl ether carboxylates; Sulfosuccinates; Aromatic sulfonates; Octylphenol ethoxylates; Ethoxylated nonylphenols; Alkyl poly (ethylene oxide); Copolymers of poly (ethylene oxide) and poly (propylene oxide); Alkyl polyglucosides such as octyl glucoside and decyl maltoside; Fatty acid alcohols such as cetyl alcohol, oleyl alcohol, cocamide MEA, cocamide DEA, alkyl hydroxy ethyl dimethyl ammonium chloride, cetyltrimethyl ammonium bromide, cetyltrimethyl ammonium chloride, hexadecyltrimethylammonium bromide and hexadecyltrimethylammonium chloride; And alkyl betaines. Specifically, the surfactant may be SLS, octylphenol ethoxylates or ethoxylated nonylphenols.

In particular, when using sodium lauryl sulfate (SLS) as the surfactant, SLS is well soluble in water due to its high degree of affinity for water and oil (HLB), Critical Michelle Concentration , CMC) is also high, even if excessively added, does not inhibit the formation of the polyamide active layer.

In one embodiment of the present specification, the content of the surfactant may be 0.01wt% to 1wt% based on 100wt% of the composition for polyamide interfacial polymerization.

In one embodiment of the present specification, the composition for polyamide interfacial polymerization may include water as a solvent, and the remainder except for the amine compound, the pyrimidine compound, the purine compound, and the surfactant may be water in the composition. .

One embodiment of the present specification comprises the steps of preparing a porous support; And forming a polyamide active layer on the porous support by interfacially polymerizing the polyamide interfacial polymerization composition and the acyl halide compound.

In one embodiment of the present specification, the preparing of the porous support may be performed by coating a polymer material on a nonwoven fabric, and the type, thickness, and porosity of the nonwoven fabric may be variously changed as necessary.

Examples of the polymer material include polysulfone, polyether sulfone, polycarbonate, polyethylene oxide, polyimide, polyetherimide, polyether ether ketone, polypropylene, polymethylpentene, polymethyl chloride and polyvinylidene fluoride. Etc. may be used, but is not necessarily limited thereto.

In one embodiment of the present specification, the polymer material may be polysulfone.

In an exemplary embodiment of the present specification, the forming of the polyamide active layer comprises: forming an aqueous solution layer including a composition for polyamide interfacial polymerization on the porous support; And contacting an organic solution including an acyl halide compound and an organic solvent on the aqueous solution layer.

Upon contact of the aqueous solution layer comprising the polyamide interfacial polymerization composition with the organic solution, an amine compound and an acyl halide compound coated on the surface of the porous support react with each other to generate polyamide by interfacial polymerization, and a microporous support. Is adsorbed to form a thin film. The contact method may be a method such as dipping, spraying or coating.

In an exemplary embodiment of the present specification, a method of forming an aqueous solution layer including the polyamide interfacial polymerization composition on the porous support is not particularly limited, and any method capable of forming an aqueous solution layer on the support is not limited. Can be used. Specifically, spraying, coating, dipping or dripping etc. are mentioned.

In one embodiment of the present specification, the aqueous solution layer may be additionally subjected to a step of removing the aqueous solution containing the excess amine compound as necessary. The aqueous solution layer formed on the porous support may be unevenly distributed when there are too many aqueous solutions present on the support. When the aqueous solution is unevenly distributed, a nonuniform polyamide active layer may be formed by subsequent interfacial polymerization. . Therefore, it is preferable to remove excess aqueous solution after forming an aqueous solution layer on the said support body. The removal of the excess aqueous solution is not particularly limited, but may be performed using, for example, a sponge, air knife, nitrogen gas blowing, natural drying, or a compression roll.

The acyl halide compound is not limited as long as it can be used for the polymerization of polyamide, but an aromatic compound having two or three carboxylic acid halides, for example, trimezoyl chloride (TMC), isophthaloyl chloride and One or a mixture of two or more selected from the group of compounds consisting of terephthaloyl chloride may be preferably used, and trimesoyl chloride (TMC) may be preferably used.

In one embodiment of the present specification, it is preferable that the organic solvent does not participate in an interfacial polymerization reaction, and an aliphatic hydrocarbon solvent, for example, isoparaffin-based mixture of freons and alkanes and alkanes having 5 to 12 carbon atoms. It may include one or more selected from solvents. Specifically, 1 selected from hexane, heptane, octane, nonane, decane, undecane, dodecane, cyclohexane, IsoPar (Exxon), IsoPar G (Exxon), ISOL-C (SK Chem) and ISOL-G (Exxon) More than one species may be used, but this is not limiting.

The content of the acyl halide compound may be 0.05 wt% to 1 wt%, preferably 0.08 wt% to 0.8 wt%, and more preferably 0.05 wt% to 0.6 wt%, based on 100 wt% of the organic solution.

Production of a homogeneous polyamide layer is possible when the content of acyl halide compound is in the above range.

One embodiment of the present specification is a porous support; And

It is provided on the porous support, and provides a water treatment separation membrane comprising a polyamide active layer comprising a pyrimidine compound and a purine compound.

In one embodiment of the present specification, the salt removal rate of the water treatment membrane is 99% or more, preferably 99.6% or more, more preferably 99.7% or more.

The salt removal rate is based on the value measured when an aqueous solution containing 2,000 ppm of NaCl was passed at 25 ° C. for 60 minutes at a pressure of 150 psi and a flow rate of 4.5 L / min.

Each configuration of the water treatment separation membrane may be referred to the description of the polyamide interfacial polymerization composition and the method for producing the water treatment separation membrane.

1 illustrates a water treatment separation membrane according to an exemplary embodiment of the present specification. Specifically, FIG. 1 illustrates a water treatment separator in which a nonwoven fabric 100, a porous support layer 200, and a polyamide active layer 300 are sequentially provided, and raw water 400 including impurities as a polyamide active layer 300. Is introduced, purified water 500 is discharged through the nonwoven fabric 100, the concentrated water 600 is not passed through the polyamide active layer 300 is discharged to the outside. However, the water treatment membrane according to one embodiment of the present specification is not limited to the structure of FIG. 1, and may further include an additional configuration.

In one embodiment of the present specification, the water treatment separation membrane may be a micro filtration membrane (Ultra Filtration), an ultra filtration membrane (Ultra Filtration), a nano filtration membrane (Nano Filtration) or a reverse osmosis membrane (Reverse Osmosis), specifically, may be a reverse osmosis membrane .

One embodiment of the present invention provides a water treatment module including at least one or more of the aforementioned water treatment separation membrane.

A specific kind of the water treatment module is not particularly limited, and examples thereof include a plate & frame module, a tubular module, a hollow & fiber module or a spiral wound module. In addition, as long as the water treatment module includes the reverse osmosis membrane according to one embodiment of the present specification described above, other configurations and manufacturing methods are not particularly limited, and general means known in the art may be employed without limitation. .

On the other hand, the water treatment module according to an exemplary embodiment of the present specification has excellent salt removal rate and boron removal rate, so it can be usefully used for water treatment devices such as domestic / industrial water purification devices, sewage treatment devices, seawater treatment devices and the like.

Hereinafter, the present invention will be described in detail with reference to Examples. However, embodiments according to the present disclosure may be modified in various other forms, and the scope of the present disclosure is not interpreted to be limited to the embodiments described below. The embodiments of the present specification are provided to more fully describe the present specification to those skilled in the art.

Example: Preparation of Water Treatment Membrane

Comparative Example 1.

18 wt% of polysulfone solids were added to a DMF (N, N-dimethylformamide) solution and dissolved at 80 ° C. to 85 ° C. for at least 12 hours to obtain a uniform liquid phase. The solution was cast 150 μm thick on a 95 μm to 100 μm thick nonwoven fabric made of polyester. Then, the cast nonwoven fabric was put in water to prepare a porous polysulfone support having a porosity of 70%.

For polyamide interfacial polymerization comprising 8wt% m-phenylenediamine (mPD) based on 100wt% of the composition on the support, 0.06wt% of sodium lauryl sulfate (SLS) as a surfactant and the balance of water The composition was applied to form an aqueous layer.

Subsequently, an organic solution containing 0.25 wt% of trimezoyl chloride (TMC) and 99.75 wt% of Isopar-G was coated on the aqueous solution layer to form an organic layer to perform an interfacial polymerization to form a polyamide active layer to prepare a water treatment separation membrane. It was.

Example 1.

A water treatment separation membrane was manufactured in the same manner as in Comparative Example 1, except that 0.005 wt% of uracil and 0.01 wt% of guanine were added to the polyamide interfacial polymerization composition in Comparative Example 1.

Example 2.

A water treatment separation membrane was manufactured in the same manner as in Comparative Example 1, except that 0.01 wt% of uracil and 0.01 wt% of guanine were added to the polyamide interfacial polymerization composition in Comparative Example 1.

Example 3.

A water treatment separation membrane was manufactured in the same manner as in Comparative Example 1, except that 0.05 wt% of uracil and 0.01 wt% of guanine were added to the polyamide interfacial polymerization composition in Comparative Example 1.

Example 4.

A water treatment separation membrane was manufactured in the same manner as in Comparative Example 1, except that 0.1 wt% of uracil and 0.01 wt% of guanine were added to the polyamide interfacial polymerization composition in Comparative Example 1.

Example 5.

A water treatment separation membrane was manufactured in the same manner as in Comparative Example 1, except that 0.05 wt% of uracil and 0.005 wt% of guanine were added to the polyamide interfacial polymerization composition in Comparative Example 1.

Example 6.

A water treatment separation membrane was manufactured in the same manner as in Comparative Example 1, except that 0.05 wt% of uracil and 0.05 wt% of guanine were added to the polyamide interfacial polymerization composition in Comparative Example 1.

Example 7.

A water treatment separation membrane was manufactured in the same manner as in Comparative Example 1, except that 0.05 wt% of uracil and 0.1 wt% of guanine were added to the polyamide interfacial polymerization composition in Comparative Example 1.

Example 8.

A water treatment separation membrane was manufactured in the same manner as in Comparative Example 1, except that 0.05 wt% of uracil and 0.01 wt% of xanthine were added to the polyamide interfacial polymerization composition in Comparative Example 1.

Example 9.

A water treatment separation membrane was manufactured in the same manner as in Comparative Example 1, except that 0.05 wt% of cytosine and 0.01 wt% of guanine were added to the polyamide interfacial polymerization composition in Comparative Example 1.

Example 10.

A water treatment separation membrane was manufactured in the same manner as in Comparative Example 1, except that 0.05 wt% of thymine and 0.01 wt% of guanine were added to the polyamide interfacial polymerization composition in Comparative Example 1.

Experimental Example: Performance Evaluation of Water Treatment Membrane

In order to measure the salt removal rate and permeate flow rate (GFD) of the water treatment membranes prepared according to the examples and comparative examples, a water treatment module including a flat plate permeation cell, a high pressure pump, a reservoir and a cooling device was used. The plate-type transmission cell had an effective transmission area of 28 cm 2 in a cross-flow manner. The water treatment membrane was installed in the permeation cell and then preliminarily operated for about 1 hour using tertiary distilled water to stabilize the evaluation equipment.

Then, after confirming that the 2,000 ppm NaCl aqueous solution was stabilized by operating the equipment for about 1 hour at a flow rate of 150 psi and 4.5 L / min, the permeate flow rate (flux: gfd ( gallon / ft ² / day)), and the salt removal rate was calculated by analyzing the salt concentration before and after permeation using a conductivity meter (Conductivity Meter) is shown in Table 1 below.

Types of pyrimidine compounds Content of pyrimidine compound (wt%) Types of Purine Compounds Content of Purine Compound (wt%) Salt removal rate
(%) Permeate flow rate
(GFD) Comparative Example 1 - 0 - 0 99.58 17.01 Example 1 Uracil 0.005 Guanine 0.01 99.66 15.88 Example 2 Uracil 0.01 Guanine 0.01 99.64 16.26 Example 3 Uracil 0.05 Guanine 0.01 99.72 18.48 Example 4 Uracil 0.1 Guanine 0.01 99.74 15.95 Example 5 Uracil 0.05 Guanine 0.005 99.62 17.51 Example 6 Uracil 0.05 Guanine 0.05 99.6 16.56 Example 7 Uracil 0.05 Guanine 0.1 99.67 16.17 Example 8 Uracil 0.05 Xanthine 0.01 99.64 16.44 Example 9 Cytosine 0.05 Guanine 0.01 99.68 18.55 Example 10 Thymine 0.05 Guanine 0.01 99.71 18.03

Looking at the results of Table 1, according to an exemplary embodiment of the present specification, the water treatment separation membranes of Examples 1 to 10 including the pyrimidine-based compound and the purine-based compound do not include the pyrimidine-based compound and the purine-based compound. Compared to the water treatment membrane of Example 1, the permeate flow rate can be confirmed that the salt removal rate is high while maintaining a similar level or more improved level. That is, when the water treatment separation membrane was prepared using the polyamide interfacial polymerization composition according to one embodiment of the present specification, it was proved that the salt removal rate was improved without a decrease in the permeate flow rate.

100: nonwoven
200: porous support layer
300: polyamide active layer
400: raw water containing impurities
500: purified water
600: concentrated water

Claims (12)

A composition for polyamide interfacial polymerization comprising an amine compound, a pyrimidine compound and a purine compound. The method according to claim 1,
The pyrimidine-based compound is a polyamide interfacial polymerization composition comprising at least one selected from a carbonyl group and a hydroxy group. The method according to claim 1,
The pyrimidine-based compound is a composition for polyamide interfacial polymerization that is one or more selected from uracil (Uracil), cytosine (Cytosine) and thymine (Thymine). The method according to claim 1,
The purine-based compounds are purine, adenine, guanine, hypoxanthine, xanthine, theobromine, caffeine, uric acid, and iso The composition for polyamide interfacial polymerization that is at least one selected from guanine (isoguanine). The method according to claim 1,
The content of the pyrimidine-based compound is a composition for polyamide interfacial polymerization is 0.001wt% to 1wt% based on 100wt% of the polyamide interfacial polymerization composition. The method according to claim 1,
The content of the purine-based compound is a polyamide interfacial polymerization composition of 0.001wt% to 1wt% based on 100wt% of the polyamide interfacial polymerization composition. The method according to claim 1,
The content of the amine compound is a polyamide interfacial polymerization composition of 0.1wt% to 20wt% based on 100wt% for the polyamide interfacial polymerization. The method according to claim 1,
The polyamide surfactant composition further comprises a surfactant,
The content of the surfactant is a composition for polyamide interfacial polymerization is 0.01wt% to 1wt% based on 100wt% of the polyamide interfacial polymerization composition. Preparing a porous support; And
A method for producing a water treatment separation membrane comprising the step of interfacially polymerizing the polyamide interfacial polymerization composition and acyl halide compound according to claim 1 to form a polyamide active layer on the porous support. Porous support; And
A polyamide active layer provided on the porous support and including a pyrimidine compound and a purine compound
Water treatment membrane comprising a. The method according to claim 10,
A water treatment separation membrane having a salt removal rate of 99% or more when an aqueous solution containing 2,000 ppm of NaCl is passed at a temperature of 150 psi and a flow rate of 4.5 L / min at 25 ° C. for 60 minutes. A water treatment module comprising at least one water treatment separation membrane according to claim 10 or 11.

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