KR20100007245A - Asymmetric hollow fiber membranes and preparation thereof - Google Patents

Abstract

PURPOSE: An asymmetric hollow fiber membrane and a manufacturing method thereof are provided to offer high intensity, high water transmission property, good mechanical strength and hardness without additional processes. CONSTITUTION: A manufacturing method of a hollow fiber membrane includes the following steps: discharging internal coagulant from a triple-layered nozzle; discharging a solvent to the outside; and discharging a thermosetting resin solution from the nozzles. The manufacturing method of the membrane further includes a step for discharging the internal coagulant from a double-layered nozzle, and a step for solidifying the thermosetting resin solution.

Description

Asymmetric Hollow Fiber Membrane and Manufacturing Method Thereof {Asymmetric Hollow Fiber Membranes and Preparation Thereof}

The present invention relates to an asymmetric hollow fiber membrane and a method for manufacturing the same, and more particularly, to form a support layer to maintain the strength and support the shape of the membrane inside the hollow fiber, the branched structure layer to the top of the support layer And asymmetric porous hollow fiber membranes having a high water permeability and high water permeability by sequentially forming a separation active layer and a method for preparing the same.

Recently, various membranes and membrane separation processes using the same have been actively developed in various fields of application for the purpose of energy saving and environmental protection.

In particular, the ultrafiltration membrane or microfiltration membrane is not only water treatment field such as wastewater treatment, industrial water production, pretreatment in seawater desalination process, but also food industry field such as microorganism separation from fermentation broth, protein purification, juice concentration process, cell culture, and pharmaceutical separation. It has been applied to various fields, such as medical industry.In particular, since its use in water purification facilities after Cryptosporidium accident occurred in 1993 in Milwaukee, Wisconsin, USA, its use has been expanded. In addition, in recent years in the United States, Europe, Japan, etc., the introduction of the membrane process as a water treatment facility has been actively studied.

However, the water treatment using the separation membrane is still able to withstand chemical cleaning despite the advantages of concentrating a device capable of treating a large amount of water with a small installation area, ease of scale expansion, ease of operation and maintenance cost. In addition to the chemical resistance and durability due to frequent physical cleaning, the unique characteristics of the membrane such as high permeability, filtration, and disinfection are required.The selection of membrane material with high fouling resistance to maintain permeability even during long-term operation There is a need for separators having these characteristics.

Recently, polyvinylidene fluoride-based polymers have been attracting attention as a material well suited to these characteristics, which are known to have excellent mechanical and chemical properties compared to other polymer materials, and have been used for a long time in coatings, piezoelectric materials, transport pipes, and separation materials. It has been used a lot of materials, and in recent years has also been researched in the use of a separator for secondary batteries.

Meanwhile, materials that can be used as separators such as porous hollow fiber membranes or plate-shaped porous membranes are generally polycarbonate, polyvinylidene luoride, polytetrafluoroethylene, and polypropylene. (polypropylene), polyamide, cellulose esters, polysulfone, polyetherimide, polyetheretherketone, polyethersulfone, polyacrylonitrile (polyacrylonitrile), polyimide, and the like.

As described above, the polymer material used as the separator may have a different manufacturing method according to its characteristics, such as a stretching method, a phase transition method, a coating method, a track etching method, or a sintering method.

Here, the phase transition method is thermal induced phase separation method, non-solvent induced phase separation method, solvent-vapor induced phase separation method, non-solvent vapor induction phase separation method ( Vapor induced phase separation).

The thermal induction phase separation method is a method of achieving a porous membrane by contacting a polymer solution dissolved at a high temperature with a low temperature medium to generate a liquid-solid phase separation and solidification, and the solvent induction phase separation method is a polymer in a solvent capable of dissolving the polymer. By dissolving the solvent and the non-solvent in the polymer solution, the interchange is performed to induce liquid-solid phase separation and solidification to achieve a porous separator.

Meanwhile, solvents for dissolving the polymer may be classified into good solvents, poor solvents, and non-solvents according to the degree of dissolution. A good solvent is a solvent capable of dissolving more than 5 parts by weight of a polymer at a temperature of about 60 ° C. or lower, and polyvinylidene fluoride. Methylpyrrolidone (N, N-methyl-2-pyrrolidone), dimethylsulfoxide, dimethylacetamide, dimethylformamide, acetone, etc. All.

The poor solvent may not dissolve the polymer at 5 wt% or more at a low temperature of 60 ° C. or lower, but may be dissolved in the polyvinylidene fluoride polymer as a solvent that may dissolve 5 wt% or more at a high temperature range of 60 ° C. or higher or below the melting point of the polymer. Gamma-butyrolactone, dimethyl phthalate, dibutyl phthalate, dioctyl phthalate, cyclohexanone, and the like. Solvents that do not dissolve or swell polymers up to the boiling point are defined as nonsolvents, which include water, ethylene glycol, diethyleneglycol, methanol, ethanol, hexane, Benzene and the like are typical.

 For example, Korean Patent Publication No. 2005-18624 discloses a porous membrane having both a three-dimensional mesh structure and a spherical structure, which dissolve a thermoplastic resin in a solvent and discharge the resin solution from a spinning nozzle into a cooling liquid. To solidify to form a porous membrane.

At this time, by changing the composition of the cooling liquid on one side and the other side of the porous membrane to prepare a porous membrane having both three-dimensional mesh structure and spherical structure.

As another example, Bulte et al., Published in 1996, described in A.M.W. Bulte, M.H.V. Mulder, C. A. Smolders, H. Strathmann, Diffusion induced separation with crystallizable nylons. II. Relation to final membrane morphology, Journal of Membrane Science, 121, 51-58 (1996)] is used to prepare a membrane using a thermoplastic resin. The production is started.

As another example, Lee et al., Published in 1994, S.-G. Li, G.H. Koops, M.H.V. Mulder, T. van den Boomgaard, C.A. Smolders, Wet spinning of integrally skinned hollow fiber membranes by a modified dual-bath coagulation method using a triple orifice spinneret, Journal of membrane science, 94, 329-340 (1994), and Albretz, et al. W. Albrecht, K. Kneifel, Th. Weigel, R. Hilke, R. Just, M. Schossig, K. Ebert, A. Lendlein, Preparation of highly asymmetric hollow fiber membranes from poly (ether imide) by a modified dry-wet phase inversion technique using a triple spinneret, Journal of membrane science, 262, 69-80 (2005)] discloses the production of hollow fiber membranes for pervaporation using triple spinning nozzles.

The present invention has a problem to be solved to provide a hollow fiber membrane having a high strength, high permeability performance, high rejection rate and excellent mechanical strength and hardness and a manufacturing method thereof without complicated and additional processes such as stretching.

In one aspect, the present invention is a support layer having an amorphous structure having a large pore inside the separator is formed, the branched structure layer and the separation active layer produced by the non-solvent induction phase separation method to the top of the support layer is formed sequentially It provides a hollow fiber membrane comprising a.

In another aspect, the present invention is to manufacture the hollow fiber membrane, characterized in that the internal coagulating solution is discharged from the triple nozzle to the inside, the good solvent is discharged to the outside, and the thermosetting resin solution is discharged from the nozzle between the inside and the outside Provide a method.

In another aspect, the present invention is hollow, characterized in that the internal coagulating solution is discharged from the double nozzle, the thermosetting resin solution is discharged to the outside to solidify and then pass the good solvent continuously and then pass the non-solvent It provides a method for producing a four separation membrane.

The hollow fiber separation membrane according to the present invention may be any separation membrane used for water treatment such as water treatment, drainage treatment, beverage preparation, and wastewater treatment, and preferably any separation membrane having a hollow, and may be separately referred to as a filtration membrane or a membrane. .

Such hollow fiber separator has a support layer having an amorphous structure having macropores in the separator, and the branched structure layer and the separation active layer manufactured by the non-solvent inductive phase separation method are sequentially formed on top of the support layer. Is formed.

Here, the support layer is formed in the hollow fiber membrane to support the hollow fiber membrane, and is not particularly limited as long as it is a support layer for this purpose, but preferably has an amorphous structure having macropores, and more preferably heat It is preferable that it is in the form of agglomerates formed by induction phase separation or modified thermal induction phase separation.

At this time, the amorphous structure having a large pore is a plurality of irregular lump-shaped piles are connected to each other, the gap between the pile and the pile pores that are much larger than the normal pores, for example, the average length is 1 to 100㎛ And, means a structure having a crack having an average width of 0.1 to 10㎛, which allows to prepare a high strength separation membrane while maintaining the permeation performance of the separation membrane.

Meanwhile, the thermal induction phase separation method or the modified thermal induction phase separation method, which is a method of forming a lump-shaped dummy constituting the support layer, is not particularly limited as long as it is a thermal induction phase separation method or a modified thermal induction phase separation method commonly used in the art. For example, the thermally induced phase separation method refers to preparing a membrane by contacting a polymer solution dissolved at a high temperature with a low temperature medium to generate liquid-solid phase separation and solidification.

In a particular embodiment, the support layer according to the present invention comprises 20 to 60% by weight of the thermosetting resin based on the total support layer weight; Poor solvent 30 to 50% by weight; 0.1 to 10 weight percent organic additive; 0.1-20 wt% of inorganic additives; And 0.1 to 5% by weight of nonsolvent.

In another specific embodiment, the support layer according to the present invention comprises 20 to 60% by weight of the thermosetting resin based on the total support layer weight; Poor solvent 30 to 50% by weight; 0.1 to 10 weight percent organic additive and 0.1 to 5 weight percent nonsolvent.

In another specific embodiment, the support layer according to the present invention comprises 20 to 60% by weight of the thermosetting resin based on the total support layer weight; Poor solvent 30 to 50% by weight; 0.1 to 10 weight percent organic additive; 0.1-20 wt% of inorganic additives; 0.1 to 5% by weight of non-solvent and 0.01 to 1% by weight of surfactant.

In another specific embodiment, the support layer according to the present invention comprises 20 to 50% by weight of the thermosetting resin based on the total support layer weight; Poor solvent 30 to 50% by weight; Good solvent 1 to 20% by weight; 0.1 to 10 weight percent organic additive; 0.1-20 wt% of inorganic additives; It may be composed of 0.1 to 5% by weight non-solvent.

Here, in the thermosetting resin, the polyvinylidene fluoride is preferably a weight average molecular weight of 150,000 to 700,000 Da (Dalton).

In addition, the organic additive may be polyvinylpyrrolidone having a weight average molecular weight of 10,000 to 90,000 Da, polyethylene glycol, maleic anhydride or polyvinyl alcohol of a weight average molecular weight of 200 to 1,000 Da, and the inorganic additive may be lithium chloride, Sodium chloride and calcium chloride are recommended.

In addition, the non-solvent is preferably water, ethylene glycol, diethylene glycol or a mixture thereof, and the surfactant is preferably sodium dodecyl sulfate, linear alkyl sulfonate or a mixture thereof.

Branch structure layer according to the present invention is formed on the top of the support layer for supporting the hollow fiber membrane, may coexist in any form with the support layer, in order to maintain a high level of strength, permeability and rejection, etc. It is preferable to have a form stacked on top of the support layer.

Here, the branched structure layer is preferably formed with a plurality of pores having a size of 5 to 100㎛. In this case, the branched structure refers to a structure in which the pores are formed long in the outer diameter direction from the inner center of the hollow fiber membrane.

The separation active layer according to the present invention is formed on top of the branched structure layer to provide an appearance of the hollow fiber membrane and at the same time to substantially separate the solids and water contained in the water to be treated, Any conventional separating active layer may be used, but it is preferable to have a form stacked on top of the branched structure layer in order to maintain a high level of strength, permeability and rejection ratio, and more preferably. Is preferably formed a plurality of pores having a size of 0.001 to 0.1㎛.

Meanwhile, the hollow fiber membrane according to the present invention may be used as long as the hollow fiber membrane is commonly used in the art. However, the hollow fiber membrane may be preferably formed using a thermally induced phase separation method or a modified thermally induced phase separation method. It may be made of a material that can be produced, more preferably a polyvinylidene fluoride-based material, specifically polyvinylidene fluoride.

At this time, the polyvinylidene fluoride is preferably a weight average molecular weight of 150,000 to 700,000 Da (dalton).

Referring to the manufacturing method of the hollow fiber membrane according to the present invention having the above-described configuration is as follows.

Preparing a spinning solution including all or part of a polyvinylidene fluoride-based thermosetting resin, an organic additive, an inorganic additive, a good solvent, a poor solvent, and / or a non-solvent;

Preparing a hollow forming agent in which a good solvent and a non-solvent are mixed;

Preparing a redissolved solvent mixed with a good solvent or a non-solvent which redissolves the polymer solution;

The spinning solution, the hollow-forming agent and the re-solvent solvent is transferred to the triple spinning nozzle and then discharged into a coagulating solution mixed with a nonsolvent or a good solvent and a nonsolvent to prepare a hollow fiber separator.

Hereinafter, the present invention will be described in detail.

The polyvinylidene hollow fiber membrane of the present invention has a pile having a large irregular structure in the hollow fiber membrane and a support layer having a large pore structure existing between the pile and the pile, and having a thickness of 5 μm or less having micropores of 0.1 μm or less. The present invention relates to an asymmetric polyvinylidene fluoride hollow fiber separator composed of a thin separation active layer and a topographic separation active layer supporting layer having a thickness of 5 μm to 100 μm supporting the active layer between the active layer and the support layer. Preferably, the hollow fiber membrane of the present invention has a dense layer or a symmetrical structure in the surface layer of the hollow fiber membrane as in the prior art to limit the film resistance generated over the entire thickness of the hollow fiber membrane to within 5 ㎛ surface of the hollow fiber membrane As a result, not only shows excellent permeability, but also the pore size of the separation active layer is very small (0.1 μm or less), showing a high rejection rate, the hardness of the support layer is large, even if a pressure of 3 to 5 atmospheres is applied to the outside of the hollow fiber membrane. Since there is no distortion, it is advantageous to manufacture the external pressure type module, it can be kept in a low pollution state for a long time, and it is easy to control the membrane contamination, thereby providing excellent hollow fiber membrane performance.

Polyvinylidene fluoride polymer, organic additives and inorganic additives, good solvents, poor solvents, and non-solvents according to the weight average molecular weight alone or two or more thereof are mixed, and the spinning solution is maintained at 50 to 200 degrees Celsius. A polyvinylidene polymer having a weight average molecular weight of 100,000 Daltons or more and 700,000 Daltons or less may be used alone or in a mixture of two or more thereof. Rollidone, polyethylene glycol, polyvinyl alcohol, maleic anhydride and the like having a molecular weight of 200 to 20,000 Daltons may be added alone or in plurality. Lithium chloride, calcium chloride, sodium chloride, and the like may be added alone or in plurality as an inorganic additive. Is used alone or in plural, and the spinning solvent is added by adding solvent or nonsolvent alone or in plural. The production but, to prepare a polymer spinning solution by mixing with an inorganic For ionic materials the additive non-solvent is dissolved in water to form an ion having a good solvent or a poor solvent for the purpose; Blowing agent by mixing nonsolvent such as water or ethylene glycol and good solvents such as dimethylpyrrolidone, dimethylacetamide, and dimethylformamide alone or by mixing the ratio of nonsolvent and good solvent at room temperature from 2 to 8 to 8 to 2. Preparing a; Preparing a resolvent by using the good solvent alone or by mixing at room temperature with a nonsolvent such as water at a ratio of 9 to 1 to 6 to 4; The spinning solution is the central tube of the triple spinning nozzle is maintained at a temperature of 90 degrees to 210 degrees Celsius, the hollow forming agent to the inner tube of the triple spinning nozzle, 5 degrees to 80 degrees Celsius, and the re-solvent triple spinning nozzle The polyvinylidene fluoride hollow fiber membranes were simultaneously transported to the outer tube of and then discharged into a coagulating solution composed of a nonsolvent or a good solvent and a mixture of nonsolvents for the polymer and maintained at 1 to 80 degrees Celsius. Forming; Washing the hollow fiber separator with water at 20 degrees Celsius to 80 degrees Celsius; And drying after alcohol treatment.

Hereinafter, the manufacturing process of the hollow fiber membrane of the present invention in more detail,

Spinning solution manufacturing process;

Polyvinylidene fluoride-based polymer forming the hollow fiber membrane in the present invention is a weight average molecular weight of 100,000 Daltons to 700,000 Daltons, consisting of a single or a mixture of two or more, the organic additive is a weight average molecular weight of 15,000 Daltons to 90,000 Daltons Polyvinylpyrrolidone, a hydrophilic polymer or organic substance easily dissolved in water such as polyethylene glycol, polyvinyl alcohol, and maleic anhydride and a surfactant having a weight average molecular weight of 200 to 20,000 Daltons or polyvinylidene fluoride as a mixture of two or more thereof In the case of lithium chloride, an inorganic additive is added to the polymer solution by dissolving it in a good solvent or a poor solvent in case of lithium chloride, or calcium chloride or sodium chloride is dissolved in non-solvent water, ionized, and then added to the polymer solution to prepare a spinning solution. At temperatures above 120 degrees Non-re to be a well-mixed solution. Therefore, in the present invention, the spinning solution is preferably prepared at 120 to 200 degrees Celsius, and must be subjected to a defoaming process to remove the air bubbles present in the solution. In general, a hollow fiber membrane is formed by solidification at a temperature of 120 degrees Celsius or less, or a hollow fiber membrane is formed by phase separation upon contact with a non-solvent having a temperature of 120 degrees or less. Therefore, it is preferable to discharge the spinning solution into the coagulating solution through the spinning nozzle for maintaining the temperature of at least 120 degrees Celsius, preferably 130 to 180 degrees Celsius for the production of polyvinylidene fluoride hollow fiber separator. In the spinning solution, the composition ratio of each component is 30 to 60 weight percent of the polyvinylidene fluoride-based polymer, 1 to 15 weight percent of organic additives, 0 to 15 weight percent of inorganic additives, and 0 to non-solvent based on the total spinning solution composition. 10 weight percent and 30 to 60 weight percent solvent, more preferably 35 to 50 weight percent polymer material, 3 to 10 weight percent organic additive, 0 to 10 weight percent inorganic additive, 0 to nonsolvent 5 weight percent and 35-50 weight percent solvent. In the case of the polyvinylidene fluoride polymer, even when the weight average molecular weight of 100,000 Daltons is used alone, even if the weight is 50% by weight, the viscosity is relatively low, but the spinning is easy, but the mechanical strength is weak, and the single yarn is difficult to spin continuously. On the other hand, when the weight average molecular weight of 500,000 Daltons or more, even at 35 weight percent, the viscosity is very high, the spinning speed is low, and deterioration due to high temperature occurs, which is not effective.

Hollow forming agent manufacturing process;

The hollow forming agent mainly uses water or ethylene glycol as a non-solvent, and when mixing, the ratio of the good solvent to the non-solvent at room temperature is dimethyl pyrrolidone or dimethyl acetate, dimethylformamide, dimethyl sulfoxide, etc. Degassing is prepared at room temperature in two to eight to eight to two, and the temperature is maintained at 1 to 80 degrees Celsius when transported to the triple spinning nozzle.

Resolvent solvent manufacturing process;

A good solvent, dimethyl pyrrolidone or dimethyl acetate, dimethylformamide, dimethyl sulfoxide, etc. may be used alone at room temperature, or degassed by preparing a good solvent to nonsolvent ratio of 9 to 1 to 6: 4. The temperature of the furnace is maintained at 1 to 80 degrees Celsius, or when acetone is used as a resolvent solvent, it is used alone.

Preparation of hollow fiber membranes;

In the present invention, the spinning solution, the hollow-forming agent, and the resolvent solvent are simultaneously discharged into the coagulation solution using a triple spinning nozzle to form a support layer having a dummy structure, a branched active layer support layer, and a separation active layer of 5 microns or less. The hollow fiber separator which has is manufactured. At this time, the coagulation solution used in the present invention is composed of non-solvent pure water or non-solvent containing a certain amount of a solvent, the inner surface having a large pore inside by the hollow forming agent in contact with the spinning solution spinning inside It begins to form. In the case of the outer surface, the quenching occurs on the surface by the re-solvent to solidify at a moment and then re-dissolve due to the characteristics of the good solvent. As the hollow fiber membrane obtained by re-dissolving at the surface is obtained into the coagulation bath, the polymer which was re-dissolved at the surface of the hollow fiber membrane to maintain the liquid phase is reconsidered by contact with a non-solvent to form a branched active layer support layer and a separation active layer. do.

Washing process;

In addition, the present invention may further include a washing process to remove the organic matter including the solvent remaining in the membrane of the hollow fiber membranes transferred to the atmosphere from the coagulation solution. Water is preferably used as the washing liquid, and the washing time is not particularly limited, but at least one day or more and five days or less is preferable.

In a particular embodiment, the hollow fiber separator according to the present invention, as shown in Figure 1, discharge the internal coagulating solution from the triple nozzle inside, discharge the good solvent to the outside, the thermosetting resin in the nozzle between the inside and the outside It can be prepared by discharging the solution.

Here, it is good that the said good solvent is 50 degrees C or less.

1, 2 is a cooling water movement path, 4 is a resin movement path, 6 is a solvent movement path.

In another specific embodiment, the hollow fiber separation membrane according to the present invention discharges the internal coagulating solution from the double nozzle inside, discharges the thermosetting resin solution to the outside, solidifies and passes the good solvent continuously, and then passes through the non-solvent. It can manufacture.

Herein, the good solvent may have a temperature range of 5 to 150 ° C.

The hollow fiber membrane of the present invention has high water permeability and high excretion rate and maintains high strength, membrane module for water treatment, membrane module for water treatment, immersion membrane module for biofilm reactor, module for chemical mixture separation, seawater desalination The polyvinylidene fluoride-based hollow fiber membrane of the present invention can be applied to the next generation high efficiency separation process because it can be used in various ways such as a pretreatment membrane module and exhibits high economic performance and processing performance and does not cause deformation or deterioration even in long-term use. .

Hereinafter, the present invention will be described in detail through examples. However, the following examples are only for illustrating the present invention in detail and are not intended to limit the scope of the present invention by these examples.

First, prior to explaining the embodiment of the present invention, the physical properties of the hollow fiber membranes and modules prepared according to the embodiment of the present invention, such as pure permeability, rejection rate and tensile strength, elongation, etc. were measured by the following test method. .

<Measurement of Pure Permeability>

For the manufactured hollow fiber membrane module, pure water at room temperature was supplied to one side of the module in a cross flow method under 0.5 atm, and the amount of water permeated was measured, and then converted into unit time and per unit membrane area.

<Measurement of Exclusion Rate>

A 500 nanometer aqueous solution was prepared by dispersing an aqueous solution of monodisperse polystyrene particles having a size of 100 nanometers in pure water at room temperature. Particle aqueous solution was supplied to one side of the prepared module at a pressure of 0.5 atm to measure the permeated aqueous solution and the polystyrene concentration dispersed in the initially supplied raw water using an ultraviolet spectrometer (Shimadzu, UV-1601PC).

Then, the exclusion rate was determined by converting the relative ratio of the absorption peak measured at a wavelength of 240 nanometers into a percentage using the following equation.

Exclusion rate (%) = (feed water concentration-permeate concentration) ㆇ feed water concentration x 100

<Measurement of tensile strength elongation>

Tensile strength and elongation were averaged by measuring a crosshead speed 5 times at a rate of 50 millimeters per minute using a tensile tester.

Hereinafter, the present invention will be described in more detail with reference to Examples, but the present invention is not limited thereto.

<Example 1>

In order to prepare a polyvinylidene fluoride asymmetric hollow fiber membrane, to prepare a support layer using a thermal induction phase separation method, to dissolve a portion of the support layer and to re-solidify to prepare a separation active layer,

The support layer was charged with 44 parts by weight of poor solvent gamma-butyrolactone in a dissolution bath and heated to 50 degrees Celsius, and then 3 parts by weight of polyvinylpyrrolidone having an average weight of the organic additive, 19,000 daltons, was added as an inorganic additive. After adding 3 parts by weight of lithium chloride and 3 parts by weight of non-solvent diethylene glycol, the mixture was warmed up to 150 degrees Celsius, and then slowly added 47 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 440,000 Daltons, and then heated up to 180 degrees Celsius. To prepare a uniform spinning solution. The polymer solution was flowed through a middle nozzle of a triple tube of 150 degrees Celsius, and a hollow was formed by flowing an internal coagulant at room temperature mixed with dimethyl acetate and water 6 to 4 inside, and dimethyl acetate was 5 degrees Celsius outside. Spilled. All three solutions were spun into a coagulation bath consisting of water at 5 degrees Celsius and finally solidified. The dimethyl acetate flowing out is very cold compared to the polymer solution, and solidifies the surface of the polymer solution. On the other hand, dimethyl acetate is a good solvent, so that redissolved very thinly on the solidified surface and solidified again in the coagulation bath. And very dense separated active layer. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, tensile strength was 450 grams per unit hollow fiber membrane, and elongation was 35 percent. The surface scanning electron micrograph of the prepared hollow fiber membrane is shown in FIG. 1, and the scanning electron micrograph of the cross section is shown in FIG. 2. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 400 liters per unit area. The blocking rate of 100 nanometer polystyrene particles was 99 percent.

<Example 2>

In order to prepare a polyvinylidene fluoride asymmetric hollow fiber membrane, to prepare a support layer by using a strained thermal induction phase separation method, and to dissolve and re-solidify a portion of the support layer to produce a separation active layer,

The support layer was charged with 34 parts by weight of poor solvent gamma-butyrolactone and 10 parts by weight of good solvent dimethyl acetate in a dissolution tank and warmed to 50 degrees Celsius, and then the polyvinylpyrrolidone having an average weight of the organic additive of 19,000 daltons was 3 By weight, 3 parts by weight of lithium chloride and 3 parts by weight of non-solvent diethylene glycol were added as inorganic additives, and then heated to 150 degrees Celsius, and then 47 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 440,000 was gradually added. After raising the temperature to 180 degrees to prepare a uniform spinning solution. The polymer solution was flowed through a middle nozzle of a triple tube of 150 degrees Celsius, and a hollow was formed by flowing an internal coagulant at room temperature mixed with dimethyl acetate and water 6 to 4 inside, and dimethyl acetate was 5 degrees Celsius outside. Spilled. All three solutions were spun into a coagulation bath consisting of water at 5 degrees Celsius and finally solidified. The dimethyl acetate flowing out is very cold compared to the polymer solution, and solidifies the surface of the polymer solution. On the other hand, dimethyl acetate is a good solvent, so that redissolved very thinly on the solidified surface and solidified again in the coagulation bath. And very dense separated active layer. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 600 grams per unit hollow fiber membrane, and an elongation of 45 percent. The surface scanning electron micrograph of the prepared hollow fiber membrane is shown in FIG. 4, and the scanning electron micrograph of the inner surface is shown in FIG. 5. On the outer surface of the hollow fiber desert, small pores were observed in the scanning electron micrograph of 100,000 times, and the pore size was about 0.001 micron. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 450 liters per unit area. The blocking rate of 100 nanometer polystyrene particles was 98 percent.

<Example 3>

40 parts by weight of poor solvent gamma-butyrolactone, 7 parts by weight of polyvinylpyrrolidone having an average molecular weight of 19,000 organic additives, 3 parts by weight of non-diethylene glycol, and 50 parts by weight of polyvinyl fluoride having a weight average molecular weight of 322,000 A polymer solution was prepared by mixing the lithium polymer with the method of Example 1, and the polyvinylidene fluoride hollow fiber membrane was prepared by spinning the polymer solution with the method of Example 1. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 700 grams per unit hollow fiber membrane, and an elongation of 30 percent. At a transmembrane pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 250 liters per unit time. The blocking rate of 100 nanometer polystyrene particles was greater than 99 percent.

<Example 4>

40 parts by weight of poor solvent gamma-butyrolactone, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 19,000 as an organic additive, 5 parts by weight of lithium chloride as an inorganic additive, 5 parts by weight of diethylene glycol as a non-solvent, and 45 parts by weight A polyvinylidene fluoride polymer having a weight average molecular weight of 440,000 Daltons by weight was mixed by the method of Example 1 to prepare a polymer solution, and the polymer solution was spun by the method of Example 1 to prepare a polyvinylidene fluoride hollow fiber membrane. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 400 grams per unit hollow fiber membrane, and an elongation of 45 percent. At a transmembrane pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 420 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 98 percent.

Example 5

40 parts by weight of poor solvent gamma-butyrolactone, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 19,000 as an organic additive, 10 parts by weight of lithium chloride as an inorganic additive, 3 parts by weight of non-diethylene glycol, and 42 A polyvinylidene fluoride polymer having a weight average molecular weight of 440,000 parts by weight was mixed by the method of Example 1 to prepare a polymer solution, and the polymer solution was spun by the method of Example 1 to prepare a polyvinylidene fluoride hollow fiber membrane. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 500 grams per unit hollow fiber membrane, and an elongation of 40 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 380 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 98 percent.

<Example 6>

40 parts by weight of poor solvent dibutyl phthalate, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 19,000 as organic additives, 5 parts by weight of polyethylene glycol having an average molecular weight of 600, 10 parts by weight of lithium chloride as an inorganic additive, non-solvent 5 parts by weight of diethylene glycol and 35 parts by weight of a polyvinylidene fluoride polymer having a weight average molecular weight of 440,000 Daltons was mixed by the method of Example 1 to prepare a polymer solution, and the polymer solution was spun by the method of Example 1 to polyfluorinated Vinylidene hollow fiber membranes were prepared. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 450 grams per unit hollow fiber membrane, and an elongation of 50 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 430 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 98 percent.

<Example 7>

40 parts by weight of poor solvent gamma butyrolactone and 5 parts by weight of dibutyl phthalate, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 19,000 daltons as an organic additive, and 3 parts by weight of polyethylene glycol having an average molecular weight of 400 daltons, an inorganic additive 5 parts by weight of lithium chloride, 3 parts by weight of non-solvent diethylene glycol and 39 parts by weight of a polyvinylidene fluoride polymer having a weight average molecular weight of 440,000 Daltons were mixed by the method of Example 1 to prepare a polymer solution, and the polymer solution was It was spun by the method of 1 to prepare a polyvinylidene fluoride hollow fiber membrane. The manufactured hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 550 grams per unit hollow fiber membrane, and an elongation of 45 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 460 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 98 percent.

<Example 8>

44 parts by weight of poor solvent gamma butyrolactone, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 31,000 Daltons as an organic additive, 5 parts by weight of polyethylene glycol having an average molecular weight of 600 Daltons, and 3 parts by weight of lithium chloride as an inorganic additive. 3 parts by weight and 40 parts by weight of a polyvinylidene fluoride polymer having a weight average molecular weight of 440,000 Daltons was mixed by the method of Example 1 to prepare a polymer solution, and the polymer solution was spun by the method of Example 1 A polyvinylidene fluoride hollow fiber membrane was prepared. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 470 grams per unit hollow fiber membrane, and an elongation of 40 percent. At a transmembrane pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 360 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 98 percent.

Example 9

40 parts by weight of poor solvent dioctylphthalate, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 19,000 daltons as an organic additive, 5 parts by weight of polyethylene glycol having an average molecular weight of 600 daltons, 5 parts by weight of lithium chloride as an inorganic additive, A polyvinylidene fluoride polymer having a weight average molecular weight of 440,000 Daltons of 3 parts by weight and 42 parts by weight of non-solvent was mixed by the method of Example 1 to prepare a polymer solution, and the polymer solution was spun by the method of Example 1 A polyvinylidene fluoride hollow fiber membrane was prepared. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 500 grams per unit hollow fiber membrane, and an elongation of 35 percent. At a transmembrane pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 330 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 99 percent.

<Example 10>

20 parts by weight of poor solvent gamma butyrolactone and 24 parts by weight of dibutyl phthalate, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 17,000 Daltons as an organic additive and 5 parts by weight of polyethylene glycol having an average molecular weight of 200 Daltons, an inorganic additive A polyvinylidene fluoride polymer having 3 parts by weight of phosphorus lithium chloride and 3 parts by weight of non-solvent ethylene glycol and 40 parts by weight of a polyvinylidene fluoride polymer having a weight average molecular weight of 440,000 Daltons was mixed in the same manner as in Example 1 to prepare a polymer solution. The polyvinylidene fluoride hollow fiber membrane was produced by spinning by the method of Example 1. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 530 grams per unit hollow fiber membrane, and an elongation of 40 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 300 liters per unit area. The blocking rate of 100 nanometer polystyrene particles was greater than 98 percent.

<Example 11>

25 parts by weight of poor solvent gamma butyrolactone and 20 parts by weight of dioctylphthalate, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 19,000 daltons as an organic additive and 5 parts by weight of polyethylene glycol having an average molecular weight of 400 daltons, an inorganic additive A polyvinylidene fluoride polymer having 3 parts by weight of phosphorus lithium chloride and 3 parts by weight of non-solvent ethylene glycol and 39 parts by weight of a polyvinylidene fluoride polymer having a weight average molecular weight of 440,000 Daltons was mixed in the same manner as in Example 1 to prepare a polymer solution. The polyvinylidene fluoride hollow fiber membrane was produced by spinning by the method of Example 1. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 470 grams per unit hollow fiber membrane, and an elongation of 40 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 370 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 99 percent.

<Example 12>

45 parts by weight of poor solvent gamma butyrolactone, 10 parts by weight of polyvinylpyrrolidone with an average molecular weight of 17,000 Daltons as an organic additive, 5 parts by weight of diethylene glycol as a non-solvent, and a polyvinylidene fluoride polymer having a weight average molecular weight of 322,000 Daltons 16 parts by weight of a polyvinylidene fluoride polymer having a weight average molecular weight of 573,000 Daltons was mixed by the method of Example 1 to prepare a polymer solution, and the polymer solution was spun by the method of Example 1 to polyvinylidene fluoride hollow fiber membrane Was prepared. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 700 grams per unit hollow fiber membrane, and an elongation of 50 percent. At a transmembrane pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 470 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 98 percent.

Example 13

44 parts by weight of poor solvent gamma butyrolactone, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 17,000 Daltons as an organic additive, 5 parts by weight of polyethylene glycol having an average molecular weight of 600 Daltons, and 3 parts by weight of lithium chloride as an inorganic additive. , 3 parts by weight of non-solvent ethylene glycol and 16 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 322,000 daltons and 24 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 573,000 daltons by the method of Example 1 To prepare a polyvinylidene fluoride hollow fiber membrane by spinning the polymer solution by the method of Example 1. The manufactured hollow fiber membrane had an inner diameter of 0.7 millimeter and an outer diameter of 1.3 millimeter, tensile strength was 730 grams per unit hollow fiber membrane, and elongation was 50 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 430 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 99 percent.

<Example 14>

40 parts by weight of poor solvent gamma butyrolactone, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 17,000 Daltons as an organic additive, 3 parts by weight of polyethylene glycol having an average molecular weight of 400 Daltons, and 3 parts by weight of lithium chloride as an inorganic additive , 3 parts by weight of non-solvent ethylene glycol and 31 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 322,000 daltons and 15 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 687,000 daltons by the method of Example 1 To prepare a polyvinylidene fluoride hollow fiber membrane by spinning the polymer solution by the method of Example 1. The manufactured hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, the tensile strength was 800 grams per unit hollow fiber membrane, and the elongation was 30 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 290 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 99 percent.

<Example 15>

44 parts by weight of poor solvent gamma butyrolactone, 3 parts by weight of polyvinylpyrrolidone having an average molecular weight of 31,000 Daltons as an organic additive, 5 parts by weight of polyethylene glycol having an average molecular weight of 600 Daltons, and 5 parts by weight of lithium chloride as an inorganic additive. , 3 parts by weight of non-solvent ethylene glycol and 16 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 440,000 Daltons and 24 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 573,000 Daltons according to the method of Example 1 To prepare a polyvinylidene fluoride hollow fiber membrane by spinning the polymer solution by the method of Example 1. The manufactured hollow fiber membrane had an inner diameter of 0.7 millimeter and an outer diameter of 1.3 millimeter, tensile strength was 650 grams per unit hollow fiber membrane, and elongation was 40 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 390 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 99 percent.

<Example 16>

46 parts by weight of poor solvent gamma butyrolactone, 3 parts by weight of polyvinylpyrrolidone having an average molecular weight of 17,000 Daltons as an organic additive, 5 parts by weight of polyethylene glycol having an average molecular weight of 600 Daltons, and 3 parts by weight of lithium chloride as an inorganic additive. , 3 parts by weight of a non-solvent diethylene glycol and 30 parts by weight of a polyvinylidene fluoride polymer having a weight average molecular weight of 440,000 Daltons and 10 parts by weight of a polyvinylidene fluoride polymer having a weight average molecular weight of 687,000 Daltons by the method of Example 1 A solution was prepared and the polymer solution was spun by the method of Example 1 to prepare a polyvinylidene fluoride hollow fiber membrane. The prepared hollow fiber membrane had an inner diameter of 0.7 mm and an outer diameter of 1.3 mm, a tensile strength of 750 grams per unit hollow fiber membrane, and an elongation of 40 percent. At a transmembrane pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 420 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was over 99 percent.

<Example 17>

42 parts by weight of poor solvent gamma butyrolactone, 5.5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 17,000 Daltons as an organic additive, 3 parts by weight of maleic anhydride, 5 parts by weight of lithium chloride as an inorganic additive, and ethylene glycol as a non-solvent 3.5 parts by weight, 0.5 parts by weight of sodium dodecyl sulfate as a surfactant, and 20 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 322,000 daltons and 20 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 573,000 daltons To prepare a polymer solution and the polymer solution was spun by the method of Example 1 to prepare a polyvinylidene fluoride hollow fiber membrane. The manufactured hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 550 grams per unit hollow fiber membrane, and an elongation of 45 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 430 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 99 percent.

Example 18

42 parts by weight of poor solvent gamma butyrolactone, 5.5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 17,000 Daltons as an organic additive, 1 part by weight of polyvinyl alcohol, 7 parts by weight of lithium chloride as an inorganic additive, and ethylene glycol as a non-solvent To 3.5 parts by weight, 0.5 parts by weight of sodium dodecyl sulfate as a surfactant, and 16 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 322,000 daltons, and 24 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 573,000 daltons of Example 1 The polymer solution was mixed by the method, and the polymer solution was spun by the method of Example 1 to prepare a polyvinylidene fluoride hollow fiber membrane. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 600 grams per unit hollow fiber membrane, and an elongation of 45 percent. At a transmembrane pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 440 liters per unit area. The blocking rate of 100 nanometer polystyrene particles was greater than 97 percent.

Example 19

45 parts by weight of poor solvent gamma butyrolactone, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 17,000 Daltons as an organic additive, 3 parts by weight of polyethylene glycol having an average molecular weight of 600 Daltons, and 1 part by weight of sodium chloride as an inorganic additive. It was added to dissolve in water and added to the dissolution tank, and 17 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 322,000 daltons and 26 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 573,000 daltons were mixed by the method of Example 1 A polymer solution was prepared and the polymer solution was spun by the method of Example 1 to prepare a polyvinylidene fluoride hollow fiber membrane. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 600 grams per unit hollow fiber membrane, and an elongation of 45 percent. At a transmembrane pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 410 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 98 percent.

Example 20

43 parts by weight of poor solvent gamma butyrolactone, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 17,000 Daltons as an organic additive, 5 parts by weight of polyethylene glycol having an average molecular weight of 600 Daltons, and 1 part by weight of calcium chloride as an inorganic additive. It was added to dissolve in water and added to the dissolution tank, and 17 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 322,000 daltons and 26 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 573,000 daltons were mixed by the method of Example 1 A polymer solution was prepared and the polymer solution was spun by the method of Example 1 to prepare a polyvinylidene fluoride hollow fiber membrane. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, tensile strength was 800 grams per unit hollow fiber membrane, and elongation was 50 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 450 liters per unit area. The blocking rate of 100 nanometer polystyrene particles was greater than 98 percent.

Example 21

25 parts by weight of poor solvent gamma-butyrolactone and 5 parts by weight of dibutyl phthalate, 10 parts by weight of good solvent dimethylpyrrolidone, 7 parts by weight of polyvinylpyrrolidone having an average molecular weight of 17,000 daltons as an organic additive, and Polyvinylidene fluoride polymer having a weight average molecular weight of 322,000 and 3 parts by weight of ethylene glycol was mixed by the method of Example 2 to prepare a polymer solution, and the polymer solution was spun by the method of Example 2 to polyvinyl fluoride Liden hollow fiber membranes were prepared. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, tensile strength was 800 grams per unit hollow fiber membrane, and elongation was 50 percent. At a transmembrane pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 350 liters per unit time. The blocking rate of 100 nanometer polystyrene particles was greater than 99 percent.

<Example 22>

30 parts by weight of poor solvent gamma-butyrolactone, 10 parts by weight of good solvent dimethylpyrrolidone, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 19,000 daltons as an organic additive, 5 parts by weight of lithium chloride as an inorganic additive, A polyvinylidene fluoride polymer having a weight average molecular weight of 440,000 Daltons of 5 parts by weight and 45 parts by weight of non-solvent was mixed by the method of Example 2 to prepare a polymer solution, and the polymer solution was spun by the method of Example 2 A polyvinylidene fluoride hollow fiber membrane was prepared. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 770 grams per unit hollow fiber membrane, and an elongation of 55 percent. At a transmembrane pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 470 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 99 percent.

<Example 23>

30 parts by weight of poor solvent gamma-butyrolactone and 7 parts by weight of dioctylphthalate, 10 parts by weight of good solvent dimethylpyrrolidone, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 19,000 as an organic additive, and an inorganic additive 5 parts by weight of lithium chloride, 3 parts by weight of non-solvent ethylene glycol and 40 parts by weight of a polyvinylidene fluoride polymer having a weight average molecular weight of 440,000 was mixed by the method of Example 2 to prepare a polymer solution, and the polymer solution was prepared by Example 2 Spinning was carried out to prepare a polyvinylidene fluoride hollow fiber membrane. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 800 grams per unit hollow fiber membrane, and an elongation of 60 percent. At a transmembrane pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 490 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 99 percent.

<Example 24>

30 parts by weight of dibutyl phthalate as a poor solvent, 10 parts by weight of dimethyl acetate as a good solvent, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 17,000 Daltons as an organic additive and 5 parts by weight of polyethylene glycol having an average molecular weight of 200 Daltons, an inorganic additive 5 parts by weight of phosphorus lithium chloride, 5 parts by weight of non-solvent diethylene glycol and 40 parts by weight of a polyvinylidene fluoride polymer having a weight average molecular weight of 440,000 Daltons was mixed in a dissolving tank at 150 degrees Celsius to dissolve to prepare a polymer solution. The polyvinylidene fluoride hollow fiber membrane was prepared by spinning the solution by the method of Example 2 through a radiator at 140 degrees Celsius. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 850 grams per unit hollow fiber membrane, and an elongation of 60 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 500 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 99 percent.

<Example 25>

30 parts by weight of poor solvent gamma butyrolactone and 5 parts by weight of dibutyl phthalate, 10 parts by weight of good solvent dimethylpyrrolidone, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 19,000 daltons as an organic additive and 400 Daltons of average molecular weight Polyvinylidene fluoride polymer having 3 parts by weight of phosphorus polyethylene glycol, 5 parts by weight of lithium chloride as an inorganic additive, 3 parts by weight of non-solvent diethylene glycol and 39 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 440,000 Daltons was mixed in the method of Example 2 A solution was prepared and the polymer solution was spun by the method of Example 2 to prepare a polyvinylidene fluoride hollow fiber membrane. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 860 grams per unit hollow fiber membrane, and an elongation of 55 percent. At a transmembrane pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 530 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 98 percent.

Example 26

30 parts by weight of poor solvent gamma butyrolactone, 10 parts by weight of good solvent, dimethylsulfuroxide, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 31,000 Daltons, and 5 parts by weight of polyethylene glycol having an average molecular weight of 600 Daltons, 3 parts by weight of lithium chloride as an inorganic additive, 3 parts by weight of ethylene glycol as a non-solvent, and 24 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 150,000 Daltons, and 20 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 573,000 Daltons A polymer solution was prepared by mixing in the method of 2, and the polymer solution was spun by the method of Example 2 to prepare a polyvinylidene fluoride hollow fiber membrane. The manufactured hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, the tensile strength was 750 grams per unit hollow fiber membrane, and the elongation was 65 percent. At a transmembrane pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 410 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 98 percent.

Example 27

30 parts by weight of poor solvent dioctylphthalate, 10 parts by weight of good solvent dimethylpyrrolidone, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 19,000 daltons as an organic additive, 5 parts by weight of polyethylene glycol having an average molecular weight of 600 daltons, 5 parts by weight of lithium chloride as an inorganic additive, 3 parts by weight of diethylene glycol as a non-solvent, and 20 parts by weight of a polyvinylidene fluoride polymer having a weight average molecular weight of 150,000 Daltons, a weight average molecular weight of 440,000 Daltons, and a weight average molecular weight of 573,000 Daltons, respectively. 17 parts by weight and 5 parts by weight were mixed in the method of Example 2 to prepare a polymer solution, and the polymer solution was spun by the method of Example 2 to prepare a polyvinylidene fluoride hollow fiber membrane. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 880 grams per unit hollow fiber membrane, and an elongation of 50 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 520 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 97 percent.

<Example 28>

20 parts by weight of poor solvent gamma butyrolactone and 10 parts by weight of dibutyl phthalate, 14 parts by weight of good solvent dimethylpyrrolidone, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 17,000 daltons as an organic additive and an average molecular weight of 200 5 parts by weight of polyethylene glycol as dalton, 3 parts by weight of lithium chloride as inorganic additive, 3 parts by weight of ethylene glycol as non-solvent, and 40 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 440,000 Daltons were mixed by the method of Example 2. A polymer solution was prepared and the polymer solution was spun by the method of Example 2 to prepare a polyvinylidene fluoride hollow fiber membrane. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 820 grams per unit hollow fiber membrane, and an elongation of 55 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 450 liters per unit area. The blocking rate of 100 nanometer polystyrene particles was greater than 98 percent.

<Example 29>

20 parts by weight of poor solvent gamma butyrolactone and 10 parts by weight of dioctylphthalate, 10 parts by weight of good solvent dimethylpyrrolidone and 5 parts by weight of dimethyl acetate, polyvinylpyrrolidone having an average molecular weight of 19,000 daltons as an organic additive 5 5 parts by weight of polyethylene glycol having a weight part and an average molecular weight of 400 Daltons, 3 parts by weight of lithium chloride as an inorganic additive, 3 parts by weight of ethylene glycol as a non-solvent, and 39 parts by weight of a polyvinylidene fluoride polymer having a weight average molecular weight of 440,000 Daltons A polymer solution was prepared by mixing the method of Example 2, and the polymer solution was spun by the method of Example 2 to prepare a polyvinylidene fluoride hollow fiber membrane. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 730 grams per unit hollow fiber membrane, and an elongation of 60 percent. At a transmembrane pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 380 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 96 percent.

<Example 30>

35 parts by weight of poor solvent gamma butyrolactone, 10 parts by weight of good solvent dimethylpyrrolidone, 10 parts by weight of polyvinylpyrrolidone having an average molecular weight of 17,000 daltons as an organic additive, 5 parts by weight of non-diethylene glycol and 16 parts by weight of a polyvinylidene fluoride polymer having an average molecular weight of 322,000 daltons and 24 parts by weight of a polyvinylidene fluoride polymer having a weight average molecular weight of 573,000 daltons were mixed in the same manner as in Example 2 to prepare a polymer solution and the polymer solution of Example 2 Spinning was carried out to produce a polyvinylidene fluoride hollow fiber membrane. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, tensile strength was 800 grams per unit hollow fiber membrane, and elongation was 50 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 480 liters per unit area. The blocking rate of 100 nanometer polystyrene particles was greater than 98 percent.

<Example 31>

36 parts by weight of poor solvent gamma butyrolactone, 8 parts by weight of good solvent dimethyl pyrrolidone, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 17,000 Daltons as an organic additive, and 5 parts by weight of polyethylene glycol having an average molecular weight of 600 Daltons 3 parts by weight of lithium chloride as an inorganic additive, 3 parts by weight of ethylene glycol as a non-solvent, and 16 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 322,000 daltons, and 24 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 573,000 daltons. A polymer solution was prepared by mixing the method of Example 2, and the polyvinylidene fluoride hollow fiber membrane was prepared by spinning the polymer solution by the method of Example 2. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 700 grams per unit hollow fiber membrane, and an elongation of 45 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 390 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 99 percent.

<Example 32>

30 parts by weight of poor solvent gamma butyrolactone, 10 parts by weight of good solvent dimethyl pyrrolidone, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 17,000 Daltons as an organic additive, and 3 parts by weight of polyethylene glycol having an average molecular weight of 400 Daltons 3 parts by weight of lithium chloride as an inorganic additive, 3 parts by weight of ethylene glycol as a non-solvent, and 31 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 322,000 daltons, and 15 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 687,000 daltons. A polymer solution was prepared by mixing the method of Example 2, and the polyvinylidene fluoride hollow fiber membrane was prepared by spinning the polymer solution by the method of Example 2. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 850 grams per unit hollow fiber membrane, and an elongation of 45 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 400 liters per unit area. The blocking rate of 100 nanometer polystyrene particles was greater than 98 percent.

<Example 33>

30 parts by weight of poor solvent gamma butyrolactone, 10 parts by weight of good solvent dimethylsulfuroxide, 5 parts by weight of dimethylpyrrolidone, 3 parts by weight of polyvinylpyrrolidone having an average molecular weight of 31,000 daltons as an organic additive and an average molecular weight of 600 5 parts by weight of polyethylene glycol, which is Dalton, 5 parts by weight of lithium chloride, which is an inorganic additive, 3 parts by weight of ethylene glycol, which is a non-solvent, and 16 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 440,000. 24 parts by weight of vinylidene fluoride polymer was mixed by the method of Example 2 to prepare a polymer solution, and the polymer solution was spun by the method of Example 2 to prepare a polyvinylidene fluoride hollow fiber membrane. The prepared hollow fiber membrane had an internal diameter of 0.7 millimeters and an external diameter of 1.3 millimeters, a tensile strength of 800 grams per unit hollow fiber membrane, and an elongation of 50 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 500 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 99 percent.

<Example 34>

31 parts by weight of poor solvent gamma butyrolactone, 15 parts by weight of good solvent dimethylpyrrolidone, 3 parts by weight of polyvinylpyrrolidone having an average molecular weight of 17,000 Daltons as an organic additive, and 5 parts by weight of polyethylene glycol having an average molecular weight of 600 Daltons 3 parts by weight of an inorganic additive lithium chloride, 3 parts by weight of non-solvent diethylene glycol and 30 parts by weight of a polyvinylidene fluoride polymer having a weight average molecular weight of 440,000 daltons, and 10 parts of polyvinylidene fluoride polymer having a weight average molecular weight of 687,000 daltons The parts were mixed by the method of Example 2 to prepare a polymer solution, and the polymer solution was spun by the method of Example 2 to prepare a polyvinylidene fluoride hollow fiber membrane. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 850 grams per unit hollow fiber membrane, and an elongation of 45 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 450 liters per unit area. The blocking rate of 100 nanometer polystyrene particles was greater than 98 percent.

<Example 35>

32 parts by weight of poor solvent gamma butyrolactone, 10 parts by weight of dimethylpyrrolidone, 5.5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 17,000 Daltons as an organic additive, 3 parts by weight of maleic anhydride, and lithium chloride as an inorganic additive 5 Parts by weight, 3.5 parts by weight of non-solvent ethylene glycol, 0.5 parts by weight of sodium dodecyl sulfate as surfactant, and 20 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 322,000 daltons, and polyvinylidene fluoride polymer having a weight average molecular weight of 573,000 daltons. 20 parts by weight of the method of Example 2 was mixed to prepare a polymer solution, and the polymer solution was spun by the method of Example 2 to prepare a polyvinylidene fluoride hollow fiber membrane. The manufactured hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, tensile strength was 750 grams per unit hollow fiber membrane, and elongation was 45 percent. At a transmembrane pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 470 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 98 percent.

<Example 36>

32 parts by weight of poor solvent gamma butyrolactone, 10 parts by weight of good solvent dimethylpyrrolidone, 5.5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 17,000 daltons as an organic additive, 1 part by weight of polyvinyl alcohol, and inorganic additive 7 parts by weight of lithium chloride, 3.5 parts by weight of non-solvent ethylene glycol, 0.5 parts by weight of sodium dodecyl sulfate as a surfactant, and 16 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 322,000 daltons, and a polyfluoride having a weight average molecular weight of 573,000 daltons 24 parts by weight of vinylidene polymer was mixed by the method of Example 2 to prepare a polymer solution, and the polymer solution was spun by the method of Example 2 to prepare a polyvinylidene fluoride hollow fiber membrane. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 780 grams per unit hollow fiber membrane, and an elongation of 55 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 520 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 98 percent.

<Example 37>

35 parts by weight of poor solvent gamma butyrolactone, 10 parts by weight of good solvent dimethylpyrrolidone, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 17,000 Daltons as an organic additive, and 3 parts by weight of polyethylene glycol having an average molecular weight of 600 Daltons And 1 part by weight of sodium chloride, an inorganic additive, were dissolved in 3 parts by weight of water, and added to the dissolution tank. 17 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 322,000 daltons and polyvinylidene fluoride polymer having a weight average molecular weight of 573,000 daltons 26 The weight part was mixed by the method of Example 2 to prepare a polymer solution, and the polymer solution was spun by the method of Example 2 to prepare a polyvinylidene fluoride hollow fiber membrane. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, tensile strength was 800 grams per unit hollow fiber membrane, and elongation was 50 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 480 liters per unit area. The blocking rate of 100 nanometer polystyrene particles was greater than 98 percent.

<Example 38>

33 parts by weight of poor solvent gamma butyrolactone, 10 parts by weight of good solvent dimethylpyrrolidone, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 17,000 Daltons as an organic additive, and 5 parts by weight of polyethylene glycol having an average molecular weight of 600 Daltons And 1 part by weight of calcium chloride, an inorganic additive, was dissolved in 3 parts by weight of water, and added to the dissolution tank. 17 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 322,000 daltons and polyvinylidene fluoride polymer having a weight average molecular weight of 573,000 daltons 26 The weight part was mixed by the method of Example 1 to prepare a polymer solution, and the polymer solution was spun by the method of Example 1 to prepare a polyvinylidene fluoride hollow fiber membrane. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 850 grams per unit hollow fiber membrane, and an elongation of 60 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 550 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 99 percent.

<Example 39>

A polymer solution was prepared by mixing in the same manner as in Example 2 with the composition of Example 35, and prepared by using a hollow forming agent for flowing a mixture of dimethyl acetate and water in a ratio of 8 to 2. Vinylidene fluoride hollow fiber membranes were prepared. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 600 grams per unit hollow fiber membrane, and an elongation of 42 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 570 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 92 percent.

<Example 40>

A polymer solution was prepared by mixing in the same manner as in Example 2 with the composition of Example 35, and prepared as a hollow forming agent for flowing a mixture of dimethyl acetate and water in a ratio of 5 to 5. Vinylidene fluoride hollow fiber membranes were prepared. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, tensile strength was 800 grams per unit hollow fiber membrane, and elongation was 50 percent. At a transmembrane pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 470 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 98 percent.

<Example 41>

A polymer solution was prepared by mixing in the method of Example 2 with the composition of Example 35, and prepared with a hollow forming agent that flows the mixture of dimethyl acetate and water 6 to 4 inside to maintain a triple spinning nozzle while maintaining 5 degrees Celsius The polyvinylidene fluoride hollow fiber membrane was produced by spinning by the method of Example 2, conveying into. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 650 grams per unit hollow fiber membrane, and an elongation of 35 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 400 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 95 percent.

<Example 42>

A polymer solution was prepared by mixing in the method of Example 2 with the composition of Example 35, and prepared with a hollow forming agent that flows the mixture of dimethyl acetate and water in 6 to 4 into a triple spinning nozzle while maintaining 50 degrees Celsius. The polyvinylidene fluoride hollow fiber membrane was produced by spinning by the method of Example 2, conveying. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 700 grams per unit hollow fiber membrane, and an elongation of 45 percent. At a transmembrane pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 420 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 97 percent.

<Example 43>

A polymer solution was prepared by mixing in the same manner as in Example 2 with the composition of Example 35, and prepared as a hollow forming agent for flowing a mixture of dimethylpyrrolidone and water in 6 to 4 into the spinning agent according to Example 2 To produce a polyvinylidene fluoride hollow fiber membrane. The manufactured hollow fiber membrane had an inner diameter of 0.7 millimeter and an outer diameter of 1.3 millimeter, tensile strength was 780 grams per unit hollow fiber membrane, and elongation was 52 percent. At a membrane penetration pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 520 liters per unit area. The blocking rate of 100 nanometer polystyrene particles was greater than 98 percent.

<Example 44>

A polymer solution was prepared by mixing the composition of Example 35 using the method of Example 2. A mixture of dimethylpyrrolidone and water in a 9 to 1 ratio was prepared as a re-solvent and spun by the method of Example 2 to polyfluorinate. Vinylidene hollow fiber membranes were prepared. The manufactured hollow fiber membrane had an inner diameter of 0.7 mm and an outer diameter of 1.3 mm, a tensile strength of 880 grams per unit hollow fiber membrane, and an elongation of 35 percent. At a transmembrane pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 330 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 99 percent.

<Example 45>

A polymer solution was prepared by mixing in the same manner as in Example 2 with the composition of Example 35, and a mixture of dimethylpyrrolidone and water in 6 to 4 was prepared as a re-solvent and spun by the method of Example 2 to polyfluorinate. Vinylidene hollow fiber membranes were prepared. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 910 grams per unit hollow fiber membrane, and an elongation of 30 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 280 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 99 percent.

<Example 46>

A polymer solution was prepared by mixing in the method of Example 2 with the composition of Example 35, and a dimethylpyrrolidone and water mixed in a 9 to 1 prepared by re-dissolving solvent and transferred to a triple radiation nozzle at 10 degrees Celsius, By spinning in the method of Example 2, a polyvinylidene fluoride hollow fiber membrane was prepared. The manufactured hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, tensile strength was 480 grams per unit hollow fiber membrane, and elongation was 65 percent. At a transmembrane pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 350 liters per unit time. Polystyrene particle rejection of 100 nanometers was greater than 95 percent.

<Example 47>

A polymer solution was prepared by mixing in the method of Example 2 with the composition of Example 35, and a mixture of dimethylpyrrolidone and water 6 to 4 was prepared as a resolvent solvent and transferred to a triple radiation nozzle at 30 degrees Celsius. By spinning in the method of Example 2, a polyvinylidene fluoride hollow fiber membrane was prepared. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, tensile strength was 410 grams per unit hollow fiber membrane, and elongation was 55 percent. At a transmembrane pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 260 liters per unit time area. Polystyrene particle rejection of 100 nanometers was greater than 99 percent.

<Example 48>

A polymer solution was prepared by mixing the composition of Example 35 with the composition of Example 35. The polyvinylidene fluoride hollow was spun by the method of Example 2 while transferring acetone to a triple radiation nozzle at -10 degrees Celsius as a re-solvent. Desert was prepared. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, tensile strength of 710 grams per unit hollow fiber membrane, and elongation was 30 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 530 liters per unit time area. Polystyrene particle rejection of 100 nanometers was greater than 99 percent.

<Example 49>

The polymer solution was prepared by mixing the composition of Example 35 by the method of Example 2, and dimethyl acetate was spun by a method of Example 2 while being transported to a triple radiation nozzle at -5 degrees Celsius as a resolving solvent. A hollow fiber membrane was prepared. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 870 grams per unit hollow fiber membrane, and an elongation of 45 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 500 liters per unit time area. Polystyrene particle rejection of 100 nanometers was greater than 97 percent.

<Example 50>

A polymer solution was prepared by mixing the composition of Example 35 using the composition of Example 35, and dimethylformamide was spun by a method of Example 2 while being transported to a triple radiation nozzle at -5 degrees Celsius as a re-solvent, followed by spinning in the method of Example 2 Vinylidene hollow fiber membranes were prepared. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 760 grams per unit hollow fiber membrane, and an elongation of 50 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 480 liters per unit time area. Polystyrene particle rejection of 100 nanometers was greater than 95 percent.

<Example 51>

In Example 35, the polymer solution was prepared by mixing in the method of Example 2, and the polymer solution was transferred to a triple spinning nozzle at 120 degrees Celsius, and dimethyl acetate was transferred to a triple spinning nozzle at -5 degrees Celsius as a resolving solvent. Spinning was carried out to prepare a polyvinylidene fluoride hollow fiber membrane. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.4 millimeters, a tensile strength of 680 grams per unit hollow fiber membrane, and an elongation of 35 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 380 liters per unit time area. Polystyrene particle rejection of 100 nanometers was greater than 99 percent.

<Example 52>

A polymer solution was prepared by mixing in the method of Example 2 with the composition of Example 35, and transferred to a triple radiation nozzle at 180 degrees Celsius, and dimethylpyrrolidone was transferred to a triple radiation nozzle at -5 degrees Celsius as a remelting solvent. The polyvinylidene fluoride hollow fiber membrane was produced by spinning by the method of Example 2. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.4 millimeters, a tensile strength of 910 grams per unit hollow fiber membrane, and an elongation of 45 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 530 liters per unit time area. Polystyrene particle rejection of 100 nanometers was greater than 99 percent.

<Example 53>

The polymer solution was prepared by mixing in the composition of Example 1, and transferred to a triple spinning nozzle at 200 degrees Celsius, and dimethylpyrrolidone was transported to a triple spinning nozzle at -5 degrees Celsius at 5 degrees Celsius as a resolving solvent. To produce a polyvinylidene fluoride hollow fiber membrane. The manufactured hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.25 millimeters, a tensile strength of 860 grams per unit hollow fiber membrane, and an elongation of 65 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 330 liters per unit time area. Polystyrene particle rejection of 100 nanometers was greater than 92 percent.

<Example 54>

A polymer solution was prepared by mixing according to the composition of Example 1, and transferred to a triple spinning nozzle at 150 degrees Celsius, and dimethylpyrrolidone was filled with 2 degrees Celsius water in a coagulation bath while being transferred to a triple spinning nozzle at -5 degrees Celsius with redissolved solvent. By spinning by the method of Example 1 to prepare a polyvinylidene fluoride hollow fiber membrane. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, tensile strength was 450 grams per unit hollow fiber membrane, and elongation was 35 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 450 liters per unit time area. Polystyrene particle rejection of 100 nanometers was greater than 90 percent.

<Example 55>

A polymer solution was prepared by mixing according to the composition of Example 1 and transferred to a triple spinning nozzle at 150 degrees Celsius, and dimethylpyrrolidone was transferred to a triple radiation nozzle at -5 degrees Celsius and 5 degrees Celsius as a resolving solvent, and filled into a coagulation bath with water at 20 degrees Celsius. By spinning by the method of Example 1 to prepare a polyvinylidene fluoride hollow fiber membrane. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 400 grams per unit hollow fiber membrane, and an elongation of 40 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 320 liters per unit time unit area. Polystyrene particle rejection of 100 nanometers was greater than 93 percent.

<Example 56>

A polymer solution was prepared by mixing in the composition of Example 2, transferred to a triple spinning nozzle at 150 degrees Celsius, and dimethylpyrrolidone was transferred to a triple spinning nozzle at -5 degrees Celsius and 5 degrees Celsius as a resolvent solvent, A polyvinylidene fluoride hollow fiber membrane was prepared by spinning with 30 parts by weight of dimethylformamide in the same manner as in Example 1. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.30 millimeters, a tensile strength of 650 grams per unit hollow fiber membrane, and an elongation of 55 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 410 liters per unit time area. Polystyrene particle rejection of 100 nanometers was greater than 98 percent.

<Example 57>

A polymer solution was prepared by mixing in the composition of Example 2, and transferred to a triple spinning nozzle at 150 degrees Celsius, and dimethylpyrrolidone was transferred to a triple spinning nozzle at -5 degrees Celsius and 5 degrees Celsius as a resolvent solvent, and filled into a coagulation bath with water at 20 degrees Celsius. By spinning in the method of Example 2, a polyvinylidene fluoride hollow fiber membrane was prepared. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.30 millimeters, a tensile strength of 400 grams per unit hollow fiber membrane, and an elongation of 40 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 320 liters per unit time unit area. Polystyrene particle rejection of 100 nanometers was greater than 93 percent.

Comparative Example 1

In order to prepare a polyvinylidene fluoride asymmetric hollow fiber membrane, to prepare a support layer by using a thermal induction phase separation method, to dissolve a portion of the support layer and to re-solidify to prepare a separation active layer,

The support layer was charged with 44 parts by weight of poor solvent gamma-butyrolactone in a dissolution bath and heated to 50 degrees Celsius, and then 3 parts by weight of polyvinylpyrrolidone having an average weight of the organic additive, 19,000 daltons, was added as an inorganic additive. 3 parts by weight of lithium chloride and 3 parts by weight of non-solvent diethylene glycol were heated to 150 degrees Celsius, and then 47 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 637,000 daltons was slowly added and then heated to 180 degrees Celsius. To prepare a uniform spinning solution. The polymer solution was flowed through a middle nozzle in a triple tube of 150 degrees Celsius, but it did not spin because of its high viscosity.

Comparative Example 2

In order to prepare a polyvinylidene fluoride asymmetric hollow fiber membrane, to prepare a support layer using a thermal induction phase separation method, to dissolve a portion of the support layer and to re-solidify to prepare a separation active layer,

The support layer was charged with 44 parts by weight of poor solvent gamma-butyrolactone in a dissolution bath and heated to 50 degrees Celsius, and then 3 parts by weight of polyvinylpyrrolidone having an average weight of the organic additive, 19,000 daltons, was added as an inorganic additive. 3 parts by weight of lithium chloride and 3 parts by weight of non-solvent diethylene glycol were heated to 150 degrees Celsius, and then 47 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 637,000 daltons was slowly added and then heated to 180 degrees Celsius. To prepare a uniform spinning solution. The polymer solution was flowed through the middle nozzle of a triple tube of 200 degrees Celsius, but the viscosity was high and it was not spun.

Comparative Example 3

In order to prepare a polyvinylidene fluoride asymmetric hollow fiber membrane, to prepare a support layer by using a strained thermal induction phase separation method, and to dissolve and re-solidify a portion of the support layer to produce a separation active layer,

The support layer was charged with 44 parts by weight of a good solvent dimethylpyrrolidone in a dissolution tank and warmed to 50 degrees Celsius, and then heated to 150 degrees Celsius, and then slowly added 56 parts by weight of a polyvinylidene fluoride polymer having a weight average molecular weight of 440,000 and then 180 degrees Celsius. The temperature was raised to degrees to prepare a uniform spinning solution. The polymer solution was flowed into a middle nozzle of a triple tube of 200 degrees Celsius, and a hollow was formed by flowing an internal coagulant at room temperature mixed with 6 to 4 of dimethyl acetate and water, and dimethyl acetate was 5 degrees Celsius outside. Spilled. However, the hollow fiber membrane was not formed as the resolvent solvent boiled in contact with the polymer solution.

Comparative Example 4

44 parts by weight of poor solvent gamma butyrolactone, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 17,000 Daltons as an organic additive, 5 parts by weight of polyethylene glycol having an average molecular weight of 600 Daltons, and 3 parts by weight of lithium chloride as an inorganic additive. 10 parts by weight of non-solvent water and 16 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 322,000 daltons and 24 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 573,000 daltons were mixed in the same manner as in Example 1 This production failed and partial solidification occurred.

Comparative Example 5

40 parts by weight of poor solvent gamma butyrolactone, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 17,000 Daltons as an organic additive, 3 parts by weight of polyethylene glycol having an average molecular weight of 400 Daltons, and 3 parts by weight of lithium chloride as an inorganic additive , 3 parts by weight of non-solvent ethylene glycol and 15 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 322,000 daltons and 31 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 687,000 daltons by the method of Example 1 Was prepared, but the viscosity was not high to obtain a uniform polymer solution.

Comparative Example 6

46 parts by weight of poor solvent gamma butyrolactone, 3 parts by weight of lithium chloride as an inorganic additive, 3 parts by weight of non-diethylene glycol as a non-solvent, and 38 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 440,000 Daltons and a weight average molecular weight of 687,000 10 parts by weight of polyvinylidene fluoride polymer, which is dalton, was mixed by the method of Example 1 to prepare a polymer solution, and the polymer solution was spun by the method of Example 1 to prepare a polyvinylidene fluoride hollow fiber membrane. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, a tensile strength of 550 grams per unit hollow fiber membrane, and an elongation of 50 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 80 liters per unit time unit area. The blocking rate of 100 nanometer polystyrene particles was greater than 99 percent.

Comparative Example 7

40 parts by weight of poor solvent gamma butyrolactone, 5.5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 17,000 Daltons as an organic additive, 5 parts by weight of polyvinyl alcohol, 6 parts by weight of lithium chloride as an inorganic additive, and ethylene glycol as a non-solvent To 3.5 parts by weight and 16 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 322,000 Daltons and 24 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 573,000 Daltons in the same manner as in Example 1 to prepare a polymer solution The solution was spun by the method of Example 1 but no hollow fiber membrane was formed.

Comparative Example 8

43 parts by weight of poor solvent gamma butyrolactone, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 17,000 Daltons as an organic additive, 5 parts by weight of polyethylene glycol having an average molecular weight of 600 Daltons, and 5 parts by weight of calcium chloride as an inorganic additive. After dissolving in parts of water and adding it to a dissolution tank, 17 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 322,000 daltons and 26 parts by weight of polyvinylidene fluoride polymer having a weight average molecular weight of 573,000 daltons were mixed in the method of Example 1. The polymer solution solidified and could not be spun.

Comparative Example 9

5 parts by weight of poor solvent gamma-butyrolactone and 5 parts by weight of dibutyl phthalate, 30 parts by weight of good solvent dimethylpyrrolidone, 7 parts by weight of polyvinylpyrrolidone having an average molecular weight of 17,000 daltons as an organic additive, Polyvinylidene fluoride polymer having a weight average molecular weight of 322,000 ethylene glycol 3 parts by weight and 50 parts by weight were mixed by the method of Example 2 to prepare a polymer solution, and the polymer solution was spun by the method of Example 2 to polyvinylidene fluoride A hollow fiber membrane was prepared. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.3 millimeters, tensile strength was 700 grams per unit hollow fiber membrane, and elongation was 80 percent. At a transmembrane pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 75 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 99 percent.

Comparative Example 10

30 parts by weight of poor solvent gamma-butyrolactone, 10 parts by weight of good solvent dimethylformamide, 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 19,000 daltons as organic additive, 5 parts by weight of lithium chloride as an inorganic additive, cost Polyvinylidene fluoride polymer having a weight average molecular weight of 440,000 Daltons of 5 parts by weight and 45 parts by weight of main diethylene glycol was mixed by the method of Example 2 to prepare a polymer solution, and the polymer solution was spun by the method of Example 2 As the good solvent contained in the solution boiled and vaporized, a large pore of about 0.1 millimeter was formed on the surface of the hollow fiber membrane, and thus it was impossible to prepare a hollow fiber membrane having a separation active layer.

Comparative Example 11

20 parts by weight of poor solvent gamma butyrolactone and 5 parts by weight of dioctylphthalate, 10 parts by weight of good solvent dimethylpyrrolidone and 5 parts by weight of dimethyl acetate, and 5 parts by weight of polyvinylpyrrolidone having an average molecular weight of 19,000 daltons as an organic additive. And 10 parts by weight of maleic anhydride, 3 parts by weight of lithium chloride as an inorganic additive, 3 parts by weight of ethylene glycol as a non-solvent, and 39 parts by weight of a polyvinylidene fluoride polymer having a weight average molecular weight of 440,000 Daltons by the method of Example 2 The polymer solution was prepared and the polymer solution was spun by the method of Example 2 to prepare a polyvinylidene fluoride hollow fiber membrane, but the branched support layer supporting the separation active layer and the separation active layer was separated from the internal support layer.

Comparative Example 11

A polymer solution was prepared by mixing in the same manner as in Example 2 with the composition of Example 35, and prepared as a hollow forming agent for flowing a mixture of dimethyl acetate and water in a ratio of 1 to 9. Vinylidene fluoride hollow fiber membranes were prepared. The prepared hollow fiber membrane had an inner diameter of 0.7 mm and an outer diameter of 1.3 mm, a tensile strength of 750 grams per unit hollow fiber membrane, and an elongation of 40 percent. At a transmembrane pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 70 liters per unit time area. The blocking rate of 100 nanometer polystyrene particles was greater than 99 percent.

Comparative Example 12

A polymer solution was prepared by mixing the composition of Example 35 using the composition of Example 35. A mixture of dimethylpyrrolidone and water was mixed at a ratio of 4 to 6. No remelting occurred.

Comparative Example 13

A polymer solution was prepared by mixing the method of Example 2 with the composition of Example 35, and acetone was spun by a method of Example 2 while being transferred to a triple spinning nozzle at 30 degrees Celsius as a re-solvent, but acetone was contacted with the polymer solution. There was no surface re-dissolution due to vaporization.

Comparative Example 14

A polymer solution was prepared by mixing in the method of Example 2 with the composition of Example 35 and transferred to a triple spinning nozzle at 90 degrees Celsius, but solidified to close the nozzle.

Comparative Example 15

A polymer solution was prepared by mixing in the composition of Example 2 and transferred to a triple spinning nozzle at 250 degrees Celsius, but the hollow fiber membrane was not formed as the solvent evaporated.

Comparative Example 16

Mixing with the composition of Example 2 to prepare a polymer solution and transfer to a triple spinning nozzle at 150 degrees Celsius, and dimethylpyrrolidone is transferred to a triple radiation nozzle at -5 degrees Celsius to 5 degrees Celsius as a re-solvent, while filling the coagulation tank with water at 80 degrees Celsius By spinning in the method of Example 2, a polyvinylidene fluoride hollow fiber membrane was prepared. The prepared hollow fiber membrane had an inner diameter of 0.7 millimeters and an outer diameter of 1.30 millimeters, a tensile strength of 300 grams per unit hollow fiber membrane, and an elongation of 65 percent. At a membrane permeation pressure of 50 kilopascals and 25 degrees Celsius, the permeate flux was 65 liters per unit time area. Polystyrene particle rejection of 100 nanometers was greater than 98 percent.

As described above, those skilled in the art will understand that the present invention can be implemented in other specific forms without changing the technical spirit or essential features. Therefore, it should be understood that the embodiments described above are all illustrative and not restrictive. The scope of the present invention should be construed as being included in the scope of the present invention all changes or modifications derived from the meaning and scope of the claims to be described later rather than the detailed description and equivalent concepts thereof.

1 is a cross-sectional view of a nozzle for manufacturing a hollow fiber membrane according to the present invention,

2 is a scanning electron micrograph showing a cross section of a polyvinylidene fluoride asymmetric hollow fiber filter membrane having a spherical support layer, a separation active layer, and branched macropores as an intermediate layer;

3 is a scanning electron micrograph showing a cross section of a polyvinylidene fluoride-based asymmetric hollow fiber filtration membrane having a spherical support layer, a separation active layer, a sponge-like macropore, and a branched macropore as an intermediate layer;

4 is a scanning electron micrograph showing the inner surface of the multi-layered asymmetric polyvinylidene fluoride porous membrane to which 3 weight percent of polyvinylpyrrolidone is added.

<Description of the symbols for the main parts of the drawings>

2: Cooling water moving path 4: Resin moving path

6: solvent transfer path

Claims (21)

A hollow fiber separator comprising a support layer having an amorphous structure having macropores inside the separator, and having a branched structure layer and a separation active layer sequentially formed on top of the support layer. According to claim 1, wherein the amorphous structure having a large pore is a plurality of irregular lump-shaped piles are connected to each other, the average length of the gap between the pile and the pile is 1 to 100㎛, the average width is 0.1 to Hollow fiber membrane, characterized in that 10㎛. The hollow fiber separation membrane according to claim 1, wherein the support layer is formed in the form of agglomerates formed by a thermal induction phase separation method or a modified thermal induction phase separation method. 3. The hollow fiber separator according to claim 1 or 2, wherein the hollow fiber separator is made of polyvinylidene fluoride system. The hollow fiber membrane according to claim 1, wherein the branched structure layer is formed of a plurality of pores having a size of 5 to 100㎛. The hollow fiber separation membrane according to claim 1, wherein the separation active layer comprises a plurality of pores having a size of 0.001 to 0.1㎛. The hollow fiber separation membrane according to claim 1, wherein the separation active layer has a thickness of 0.1 to 5 µm. According to claim 1, wherein the support layer is 20 to 60% by weight of the thermosetting resin based on the total support layer weight; Poor solvent 30 to 50% by weight; 0.1 to 10 weight percent organic additive; 0.1-20 wt% of inorganic additives; And non-solvent hollow fiber membrane, characterized in that consisting of 0.1 to 5% by weight. According to claim 1, wherein the support layer is 20 to 60% by weight of the thermosetting resin based on the total support layer weight; Poor solvent 30 to 50% by weight; Hollow fiber membrane, characterized in that consisting of 0.1 to 10% by weight of the organic additive and 0.1 to 5% by weight of the non-solvent. According to claim 1, wherein the support layer is 20 to 60% by weight of the thermosetting resin based on the total support layer weight; Poor solvent 30 to 50% by weight; 0.1 to 10 weight percent organic additive; 0.1-20 wt% of inorganic additives; Hollow fiber membrane, characterized in that consisting of 0.1 to 5% by weight of non-solvent and 0.01 to 1% by weight of surfactant. According to claim 1, wherein the support layer is 20 to 50% by weight of the thermosetting resin based on the total support layer weight; Poor solvent 30 to 50% by weight; Good solvent 1 to 20% by weight; 0.1 to 10 weight percent organic additive; 0.1-20 wt% of inorganic additives; Hollow fiber membrane, characterized in that consisting of non-solvent 0.1 to 5% by weight. The hollow fiber separation membrane according to any one of claims 8 to 11, wherein the thermosetting resin is polyvinylidene fluoride. The hollow fiber membrane according to claim 12, wherein the polyvinylidene fluoride has a weight average molecular weight of 150,000 to 700,000 Da. The method according to any one of claims 8 to 11, wherein the organic additive is polyvinylpyrrolidone having a weight average molecular weight of 10,000 to 90,000 Da, polyethylene glycol, maleic anhydride or polyvinyl alcohol having a weight average molecular weight of 200 to 1,000 Da. Hollow fiber separator, characterized in that. The hollow fiber separator according to any one of claims 8 to 11, wherein the inorganic additive is lithium chloride, sodium chloride, calcium chloride. The hollow fiber membrane according to any one of claims 8 to 11, wherein the nonsolvent is water, ethylene glycol, diethylene glycol. The hollow fiber separation membrane according to claim 10, wherein the surfactant is sodium dodecyl sulfate, linear alkyl sulfonate or a mixture thereof. An internal coagulating solution is discharged from a triple nozzle, a good solvent is discharged to the outside, and a thermosetting resin solution is discharged from a nozzle between the inside and the outside. 18. The method of claim 17, wherein the good solvent is a temperature of 50 ℃ or less. A method of manufacturing a hollow fiber separator, characterized in that the internal coagulating solution is discharged from the double nozzle, the thermosetting resin solution is discharged to the outside, and then solidified. The method of claim 20, wherein the good solvent is a temperature range of 5 to 150 ℃.

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