KR101936334B1 - Hydrophilic polyolefin hollow fiber membrane for a water purifier and preparation method thereof - Google Patents
Hydrophilic polyolefin hollow fiber membrane for a water purifier and preparation method thereof Download PDFInfo
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- KR101936334B1 KR101936334B1 KR1020160113661A KR20160113661A KR101936334B1 KR 101936334 B1 KR101936334 B1 KR 101936334B1 KR 1020160113661 A KR1020160113661 A KR 1020160113661A KR 20160113661 A KR20160113661 A KR 20160113661A KR 101936334 B1 KR101936334 B1 KR 101936334B1
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- polyolefin
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- 239000012528 membrane Substances 0.000 title claims abstract description 108
- 239000012510 hollow fiber Substances 0.000 title claims abstract description 96
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 44
- 229920000098 polyolefin Polymers 0.000 title abstract description 58
- 238000002360 preparation method Methods 0.000 title 1
- 239000011247 coating layer Substances 0.000 claims abstract description 15
- -1 polypropylene Polymers 0.000 claims description 41
- 239000004743 Polypropylene Substances 0.000 claims description 22
- 229920001155 polypropylene Polymers 0.000 claims description 22
- 239000000155 melt Substances 0.000 claims description 15
- 238000000576 coating method Methods 0.000 claims description 11
- 239000011248 coating agent Substances 0.000 claims description 10
- 238000005097 cold rolling Methods 0.000 claims description 9
- 238000002074 melt spinning Methods 0.000 claims description 8
- 229920006242 ethylene acrylic acid copolymer Polymers 0.000 claims description 6
- 238000001816 cooling Methods 0.000 claims description 3
- 238000000071 blow moulding Methods 0.000 claims 1
- 229920000554 ionomer Polymers 0.000 abstract description 18
- 150000001336 alkenes Chemical class 0.000 abstract description 13
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 abstract description 13
- 230000035699 permeability Effects 0.000 abstract description 13
- 229920001400 block copolymer Polymers 0.000 description 14
- 239000004698 Polyethylene Substances 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- 229920000573 polyethylene Polymers 0.000 description 10
- 238000004519 manufacturing process Methods 0.000 description 8
- 239000002202 Polyethylene glycol Substances 0.000 description 7
- 229920001223 polyethylene glycol Polymers 0.000 description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 6
- 229920000219 Ethylene vinyl alcohol Polymers 0.000 description 6
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 4
- 229940117841 methacrylic acid copolymer Drugs 0.000 description 4
- 239000011148 porous material Substances 0.000 description 4
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 3
- UTZKJCIQQWLQPV-UHFFFAOYSA-N ethane-1,2-diol;propane-1,2-diol Chemical compound OCCO.OCCO.CC(O)CO UTZKJCIQQWLQPV-UHFFFAOYSA-N 0.000 description 3
- 229920005648 ethylene methacrylic acid copolymer Polymers 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000004804 winding Methods 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000048 melt cooling Methods 0.000 description 2
- 238000001471 micro-filtration Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000003507 refrigerant Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- 238000000108 ultra-filtration Methods 0.000 description 2
- CVEPFOUZABPRMK-UHFFFAOYSA-N 2-methylprop-2-enoic acid;styrene Chemical compound CC(=C)C(O)=O.C=CC1=CC=CC=C1 CVEPFOUZABPRMK-UHFFFAOYSA-N 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000001112 coagulating effect Effects 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 239000003651 drinking water Substances 0.000 description 1
- 235000020188 drinking water Nutrition 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000007712 rapid solidification Methods 0.000 description 1
- 238000001223 reverse osmosis Methods 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
- B01D71/06—Organic material
- B01D71/26—Polyalkenes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
- B01D71/06—Organic material
- B01D71/26—Polyalkenes
- B01D71/262—Polypropylene
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D63/00—Apparatus in general for separation processes using semi-permeable membranes
- B01D63/02—Hollow fibre modules
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D63/00—Apparatus in general for separation processes using semi-permeable membranes
- B01D63/02—Hollow fibre modules
- B01D63/021—Manufacturing thereof
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D67/00—Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
- B01D67/0002—Organic membrane manufacture
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D67/00—Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
- B01D67/0002—Organic membrane manufacture
- B01D67/002—Organic membrane manufacture from melts
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D67/00—Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
- B01D67/0002—Organic membrane manufacture
- B01D67/0023—Organic membrane manufacture by inducing porosity into non porous precursor membranes
- B01D67/0025—Organic membrane manufacture by inducing porosity into non porous precursor membranes by mechanical treatment, e.g. pore-stretching
- B01D67/0027—Organic membrane manufacture by inducing porosity into non porous precursor membranes by mechanical treatment, e.g. pore-stretching by stretching
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D67/00—Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
- B01D67/0081—After-treatment of organic or inorganic membranes
- B01D67/0083—Thermal after-treatment
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D67/00—Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
- B01D67/0081—After-treatment of organic or inorganic membranes
- B01D67/0088—Physical treatment with compounds, e.g. swelling, coating or impregnation
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D69/00—Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor
- B01D69/08—Hollow fibre membranes
- B01D69/087—Details relating to the spinning process
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
- B01D71/06—Organic material
- B01D71/26—Polyalkenes
- B01D71/261—Polyethylene
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
- B01D71/06—Organic material
- B01D71/40—Polymers of unsaturated acids or derivatives thereof, e.g. salts, amides, imides, nitriles, anhydrides, esters
- B01D71/401—Polymers based on the polymerisation of acrylic acid, e.g. polyacrylate
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
- B01D71/06—Organic material
- B01D71/76—Macromolecular material not specifically provided for in a single one of groups B01D71/08 - B01D71/74
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/001—Processes for the treatment of water whereby the filtration technique is of importance
- C02F1/003—Processes for the treatment of water whereby the filtration technique is of importance using household-type filters for producing potable water, e.g. pitchers, bottles, faucet mounted devices
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/44—Treatment of water, waste water, or sewage by dialysis, osmosis or reverse osmosis
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2323/00—Details relating to membrane preparation
- B01D2323/02—Hydrophilization
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2325/00—Details relating to properties of membranes
- B01D2325/04—Characteristic thickness
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
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- B01D2325/20—Specific permeability or cut-off range
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B01D2325/24—Mechanical properties, e.g. strength
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2325/00—Details relating to properties of membranes
- B01D2325/36—Hydrophilic membranes
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- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Water Supply & Treatment (AREA)
- Environmental & Geological Engineering (AREA)
- Hydrology & Water Resources (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Inorganic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Separation Using Semi-Permeable Membranes (AREA)
Abstract
본 발명은 폴리올레핀 중공사막; 및 상기 중공사막의 표면에 올레핀계 이오노머의 코팅층;을 포함하는 정수기용 친수성 폴리올레핀 중공사막에 관한 것이다.
본 발명에 따라 제조된 친수성 폴리올레핀 중공사막은 종래 정수기용 중공사막에 비하여 수투과도가 크게 향상되고 기계적 강도도 우수하여 정수기의 중공사막 필터로서 유용하다.The present invention relates to a polyolefin hollow fiber membrane; And a coating layer of an olefin-based ionomer on the surface of the hollow fiber membrane. The present invention also relates to a hydrophilic polyolefin hollow fiber membrane for a water purifier.
The hydrophilic polyolefin hollow fiber membrane produced according to the present invention is significantly useful as a hollow fiber membrane filter of a water purifier because it greatly improves water permeability and mechanical strength compared with the conventional hollow fiber membrane for water purifier.
Description
본 발명은 정수기용 친수성 폴리올레핀 중공사막 및 그 제조방법에 관한 것으로, 보다 상세하게는 폴리올레핀으로부터 용융방사 및 연신법에 의하여 폴리올레핀 중공사막을 얻고, 상기 중공사막의 표면에 올레핀계 이오노머를 코팅함으로써 친수성 폴리올레핀 중공사막을 제조하여 이를 정수기의 필터에 응용하는 기술에 관한 것이다.
The present invention relates to a hydrophilic polyolefin hollow fiber membrane for a water purifier and a method of producing the same, and more particularly, to a polyolefin hollow fiber membrane obtained by melt spinning and stretching method from a polyolefin and coating the surface of the hollow fiber membrane with an olefin- The present invention relates to a technique for manufacturing a hollow fiber membrane and applying it to a filter of a water purifier.
일반적으로 정수기는 물을 정수하기 위한 장치로서 침전, 여과, 살균 등의 과정을 포함한 정수법을 기초로 물에 포함된 중금속이나 기타 유해물질을 제거하여 음용수를 제공하는 장치이다. 정수기에는 물을 정수하기 위한 다양한 필터들이 구비될 수 있는데, 이러한 필터들은 그 기능에 따라 세디멘트 필터, 활성탄 필터, 정밀여과막(microfiltration membrane, MF), 한외여과막(ultrafiltration membrane, UF) 또는 역삼투막(reverse osmosis membrane, RO) 필터 등으로 구분된다.Generally, a water purifier is a device for purifying water, and is a device for removing drinking water and heavy metals contained in water based on a water purification method including precipitation, filtration and sterilization. The water purifier may be equipped with various filters for purifying the water. These filters may be classified into a sediment filter, an activated carbon filter, a microfiltration membrane (MF), an ultrafiltration membrane (UF) or a reverse osmosis membrane osmosis membrane (RO) filters.
특히, 정밀여과막 또는 한외여과막은 정수기에 적용될 뿐만 아니라, 광범위한 수처리 분야의 막분리 공정에 이용되고 있는바, 그 막의 형태로서는 중공사막 또는 평막이 모두 가능하지만 막분리 공정의 효율적 측면에서 중공사막이 주류를 이루고 있으며, 폴리프로필렌계 중공사막이 상용화되어 있다. 상기 폴리프로필렌계 중공사막은 다공질 구조로서 기계적 강도가 우수하며 그 제조과정에서 용제를 사용하지 않는 장점이 있다.
In particular, a microfiltration membrane or an ultrafiltration membrane is used not only in a water purifier but also in a membrane separation process in a wide range of water treatment fields. The membrane can be either a hollow fiber membrane or a flat membrane. However, And a polypropylene type hollow fiber membrane is commercially available. The polypropylene type hollow fiber membrane has a porous structure, which is excellent in mechanical strength and does not use a solvent in its production process.
통상적으로 상기와 같은 폴리프로필렌계 중공사막의 수투과도를 높게 하기 위해서는 막의 두께를 가능한 얇게 하는 것이 좋으나, 막의 두께를 얇게 하면 기계적 강도가 저하되고, 공극률을 높였을 때 충분한 내압성을 유지할 수 없다. 반면, 막의 두께를 두껍게 하면 기계적 강도는 향상되는데 비하여 수투과도가 떨어지는 문제점이 있으며, 폴리프로필렌계 중공사막의 경우에는 고유의 소수성 때문에 기본적으로 수투과도가 낮은 단점이 있다.
Generally, in order to increase the water permeability of the polypropylene type hollow fiber membrane, it is desirable to make the thickness of the membrane as thin as possible. However, if the thickness of the membrane is reduced, the mechanical strength is lowered and sufficient pressure resistance can not be maintained when the porosity is increased. On the other hand, when the thickness of the membrane is increased, the mechanical strength is improved and the water permeability is lowered. In the case of the polypropylene hollow fiber membrane, the water permeability is basically low because of inherent hydrophobicity.
따라서 본 발명자는 정수기용 중공사막을 제조함에 있어서, 폴리올레핀으로부터 용융방사 및 연신법에 의하여 폴리올레핀 중공사막을 얻고, 상기 중공사막의 표면에 올레핀계 이오노머를 코팅할 수 있으면, 폴리올레핀계 중공사막이 친수성으로 개질됨으로써 수투과도가 크게 향상됨과 아울러 기계적 강도도 우수한 정수기용 중공사막 필터를 얻을 수 있음에 착안하여 본 발명을 완성하기에 이르렀다.
Therefore, the inventors of the present invention have found that when a polyolefin hollow fiber membrane is obtained from a polyolefin by melt spinning and stretching method and an olefin-based ionomer is coated on the surface of the hollow fiber membrane, the polyolefin hollow fiber membrane is hydrophilic The present invention has been completed based on the fact that a hollow fiber membrane filter for a water purifier having improved water permeability and mechanical strength can be obtained.
본 발명은 상기와 같은 문제점을 감안하여 안출된 것으로, 본 발명의 목적은 종래 정수기용 폴리올레핀계 중공사막에 비하여 수투과도가 크게 향상되고 기계적 강도도 우수한 정수기용 친수성 폴리올레핀 중공사막 및 그 제조방법을 제공하고자 하는 것이다.
SUMMARY OF THE INVENTION The present invention has been made in view of the above problems, and it is an object of the present invention to provide a hydrophilic polyolefin hollow fiber membrane for a water purifier and a method for producing the hollow fiber membrane for a water purifier, which are greatly improved in water permeability and mechanical strength compared with the conventional polyolefin hollow fiber membranes I would like to.
상기한 바와 같은 목적을 달성하기 위한 본 발명은, 폴리올레핀 중공사막; 및 상기 중공사막의 표면에 올레핀계 이오노머의 코팅층;을 포함하는 정수기용 친수성 폴리올레핀 중공사막을 제공한다. To achieve these and other advantages and in accordance with the purpose of the present invention, as embodied and broadly described herein, there is provided a polyolefin hollow fiber membrane, And a coating layer of an olefin-based ionomer on the surface of the hollow fiber membrane. The present invention also provides a hydrophilic polyolefin hollow fiber membrane for a water purifier.
상기 폴리올레핀은 용융지수(MI) 0.1~10 g/10min인 폴리에틸렌 또는 폴리프로필렌인 것을 특징으로 한다.The polyolefin is characterized by being polyethylene or polypropylene having a melt index (MI) of 0.1 to 10 g / 10 min.
상기 올레핀계 이오노머는 에틸렌-아크릴산 공중합체, 에틸렌-메타크릴산 공중합체, 프로필렌-아크릴산 공중합체, 프로필렌-메타크릴산 공중합체, 에틸렌-비닐알코올 공중합체, 에틸렌-비닐술폰산 공중합체, 스티렌-메타크릴산 공중합체, 에틸렌글리콜-프로필렌글리콜-에틸렌글리콜 블록 공중합체, 스티렌-폴리에틸렌글리콜아크릴레이트 블록 공중합체, 에틸헥실메타크릴레이트-폴리에틸렌글리콜아크릴레이트 블록 공중합체 및 에틸헥실메타크릴레이트-히드록시에틸메타크릴레이트 블록 공중합체로 이루어진 군으로부터 선택된 어느 하나의 것을 특징으로 한다.The olefinic ionomer may be at least one selected from the group consisting of an ethylene-acrylic acid copolymer, an ethylene-methacrylic acid copolymer, a propylene-acrylic acid copolymer, a propylene-methacrylic acid copolymer, an ethylene-vinyl alcohol copolymer, an ethylene-vinylsulfonic acid copolymer, Ethylene glycol-propylene glycol-ethylene glycol block copolymer, styrene-polyethylene glycol acrylate block copolymer, ethylhexyl methacrylate-polyethylene glycol acrylate block copolymer, and ethylhexyl methacrylate-hydroxyethyl A methacrylate block copolymer, and a methacrylate block copolymer.
상기 코팅층은 그 두께가 0.05~1 ㎛인 것을 특징으로 한다.
The coating layer has a thickness of 0.05 to 1 占 퐉.
또한, 본 발명은 I) 폴리올레핀을 중공성형노즐을 통하여 용융방사, 냉각 및 권취하여 미연신 중공사막을 얻는 단계; II) 상기 미연신 중공사막을 100~150℃에서 1~24시간 동안 열처리한 후, 상온에서 냉연신하는 단계; III) 상기 냉연신 후, 100~200℃에서 0.1~60분 동안 열연신하여 폴리올레핀 중공사막을 형성하는 단계; 및 IV) 상기 폴리올레핀 중공사막의 표면에 올레핀계 이오노머를 코팅하는 단계;를 포함하는 정수기용 친수성 폴리올레핀 중공사막의 제조방법을 제공한다.The present invention also provides a method for producing a hollow fiber membrane, comprising the steps of: I) melt-spinning, cooling and winding a polyolefin through a hollow molding nozzle to obtain an unstretched hollow fiber membrane; II) heat treating the unstretched hollow fiber membrane at 100 to 150 ° C for 1 to 24 hours, followed by cold rolling at room temperature; III) hot-drawing the polyolefin hollow fiber membrane at a temperature of 100 to 200 ° C for 0.1 to 60 minutes after cold rolling; And IV) coating the surface of the polyolefin hollow fiber membrane with an olefin-based ionomer. The present invention also provides a method for producing a hydrophilic polyolefin hollow fiber membrane for a water purifier.
상기 폴리올레핀은 용융지수(MI) 0.1~10 g/10min인 폴리에틸렌 또는 폴리프로필렌인 것을 특징으로 한다.The polyolefin is characterized by being polyethylene or polypropylene having a melt index (MI) of 0.1 to 10 g / 10 min.
상기 올레핀계 이오노머는 에틸렌-아크릴산 공중합체, 에틸렌-메타크릴산 공중합체, 프로필렌-아크릴산 공중합체, 프로필렌-메타크릴산 공중합체, 에틸렌-비닐알코올 공중합체, 에틸렌-비닐술폰산 공중합체, 스티렌-메타크릴산 공중합체, 에틸렌글리콜-프로필렌글리콜-에틸렌글리콜 블록 공중합체, 스티렌-폴리에틸렌글리콜아크릴레이트 블록 공중합체, 에틸헥실메타크릴레이트-폴리에틸렌글리콜아크릴레이트 블록 공중합체 및 에틸헥실메타크릴레이트-히드록시에틸메타크릴레이트 블록 공중합체로 이루어진 군으로부터 선택된 어느 하나의 것을 특징으로 한다.The olefinic ionomer may be at least one selected from the group consisting of an ethylene-acrylic acid copolymer, an ethylene-methacrylic acid copolymer, a propylene-acrylic acid copolymer, a propylene-methacrylic acid copolymer, an ethylene-vinyl alcohol copolymer, an ethylene-vinylsulfonic acid copolymer, Ethylene glycol-propylene glycol-ethylene glycol block copolymer, styrene-polyethylene glycol acrylate block copolymer, ethylhexyl methacrylate-polyethylene glycol acrylate block copolymer, and ethylhexyl methacrylate-hydroxyethyl A methacrylate block copolymer, and a methacrylate block copolymer.
상기 코팅을 위한 올레핀계 이오노머 코팅용액의 농도는 0.1 내지 5 중량%인 것을 특징으로 한다.The concentration of the olefin-based ionomer coating solution for the coating is 0.1 to 5% by weight.
본 발명에 따라 제조된 친수성 폴리올레핀 중공사막은 종래 정수기용 폴리올레핀계 중공사막에 비하여 수투과도가 크게 향상되고 기계적 강도도 우수하여 정수기의 중공사막 필터로서 유용하다.
The hydrophilic polyolefin hollow fiber membrane produced according to the present invention is significantly useful as a hollow fiber membrane filter of a water purifier because it greatly improves water permeability and mechanical strength as compared with the conventional polyolefin hollow fiber membrane for water purifier.
도 1은 본 발명의 실시예 1로부터 제조된 친수성 폴리프로필렌 중공사막 표면의 모폴로지를 촬영한 주사전자현미경(SEM) 이미지.1 is a scanning electron microscope (SEM) image of the morphology of the surface of the hydrophilic polypropylene hollow fiber membrane produced from Example 1 of the present invention.
이하에서는 본 발명에 따른 정수기용 친수성 폴리올레핀 중공사막 및 그 제조방법에 대하여 첨부된 도면과 함께 상세히 설명하기로 한다.Hereinafter, a hydrophilic polyolefin hollow fiber membrane for a water purifier according to the present invention and a method for producing the same will be described in detail with reference to the accompanying drawings.
본 발명에서는, 폴리올레핀 중공사막; 및 상기 중공사막의 표면에 올레핀계 이오노머의 코팅층;을 포함하는 정수기용 친수성 폴리올레핀 중공사막을 제공한다.In the present invention, a polyolefin hollow fiber membrane; And a coating layer of an olefin-based ionomer on the surface of the hollow fiber membrane. The present invention also provides a hydrophilic polyolefin hollow fiber membrane for a water purifier.
통상적으로 폴리에틸렌 또는 폴리프로필렌과 같은 폴리올레핀 소재로부터 제조되는 중공사막은 기계적 강도가 높은 반면, 고유의 소수성으로 인하여 수투과도가 매우 낮아 그대로 수처리용 분리막 공정에 적용하기에는 한계가 있다. 또한, 상기 폴리올레핀 소재는 분자량, 결정화도, 용융지수(melt index, MI) 등의 특성에 따라 중공사막의 미세구조가 다양하게 변할 수 있는 것으로 알려져 있다.Generally, hollow fiber membranes made of a polyolefin material such as polyethylene or polypropylene have high mechanical strength, but have a very low water permeability due to inherent hydrophobicity, so that they are limited to be applied to a separation membrane process for water treatment as they are. In addition, it is known that the microstructure of the hollow fiber membrane can be variously changed according to the characteristics of the polyolefin material such as molecular weight, crystallinity, melt index (MI) and the like.
따라서 본 발명에서는 폴리올레핀 중공사막의 표면에 올레핀계 이오노머의 코팅층을 형성함으로써 폴리올레핀계 중공사막을 친수성으로 개질하였다.
Accordingly, in the present invention, the polyolefin hollow fiber membrane is modified to be hydrophilic by forming a coating layer of an olefin-based ionomer on the surface of the polyolefin hollow fiber membrane.
상기 폴리올레핀 중공사막에서 폴리올레핀으로서는 폴리에틸렌 또는 폴리프로필렌이 바람직하다. 아울러 폴리에틸렌과 폴리프로필렌의 경우에는 용융방사를 위한 인자로서 용융지수(melt index, MI)를 고려하여야 한다. 일반적으로 용융지수는 일정한 온도 및 하중에서 용융물을 피스톤에서 압출하였을 때의 유량으로, 용융물의 흐름의 용이성을 나타내는 지수로 정의되는바, ASTM D 1238 방법에 따라 폴리에틸렌은 190℃, 2.16kg의 하중에서, 폴리프로필렌은 230℃, 2.16kg의 하중에서 측정하여 g/10min 단위로 MI 지수를 결정한다.As the polyolefin in the polyolefin hollow fiber membrane, polyethylene or polypropylene is preferable. In the case of polyethylene and polypropylene, melt index (MI) should be considered as a factor for melt spinning. In general, the melt index is defined as an index representing the easiness of flow of a melt when the melt is extruded from a piston at a constant temperature and a load. According to the ASTM D 1238 method, polyethylene has a load of 190 DEG C and a load of 2.16 kg , And the polypropylene is measured at 230 ° C under a load of 2.16 kg to determine the MI index in g / 10 min units.
본 발명에서는, 균일한 다공질의 중공사막을 형성하기 위하여 용융지수(MI) 0.1~10 g/10min인 폴리에틸렌 또는 폴리프로필렌을 사용하는 것이 바람직하다. 용융지수가 0.1 g/10min 미만이면 용융점도가 너무 높아 폴리에틸렌 또는 폴리프로필렌을 안정적으로 방사하기 어렵고, 용융지수가 10 g/10min을 초과하면 용융방사된 중공사를 큰 신장율로 연신하는데 한계가 있고, 기공을 형성하지 못하거나 높은 다공성(porosity)을 얻는데 문제가 생길 수 있다. 한편, 폴리올레핀의 분자량이 용융방사를 통한 중공사막 형성에 영향을 미치는 인자라 할 수 있는데, 일반적으로 분자량과 용융지수는 트레이드-오프 관계를 가지므로 용융지수(MI) 0.1~10 g/10min인 폴리에틸렌 또는 폴리프로필렌 중에서 바람직하게 선택하여 사용한다.
In the present invention, it is preferable to use polyethylene or polypropylene having a melt index (MI) of 0.1 to 10 g / 10 min in order to form a uniform porous hollow fiber membrane. If the melt index is less than 0.1 g / 10 min, the melt viscosity is too high to stably emit polyethylene or polypropylene. If the melt index exceeds 10 g / 10 min, there is a limit to elongation of the melt- It is not possible to form pores or there may be problems in obtaining high porosity. On the other hand, the molecular weight of the polyolefin may be a factor affecting the formation of the hollow fiber membrane through the melt spinning. Generally, since the molecular weight and the melt index have a trade-off relationship, polyethylene having a melt index (MI) of 0.1 to 10 g / Or polypropylene.
또한, 상기 올레핀계 이오노머로서는 에틸렌-아크릴산 공중합체, 에틸렌-메타크릴산 공중합체, 프로필렌-아크릴산 공중합체, 프로필렌-메타크릴산 공중합체, 에틸렌-비닐알코올 공중합체, 에틸렌-비닐술폰산 공중합체, 스티렌-메타크릴산 공중합체, 에틸렌글리콜-프로필렌글리콜-에틸렌글리콜 블록 공중합체, 스티렌-폴리에틸렌글리콜아크릴레이트 블록 공중합체, 에틸헥실메타크릴레이트-폴리에틸렌글리콜아크릴레이트 블록 공중합체 및 에틸헥실메타크릴레이트-히드록시에틸메타크릴레이트 블록 공중합체로 이루어진 군으로부터 선택된 어느 하나의 것을 사용할 수 있으며, 에틸렌-아크릴산 공중합체 또는 에틸렌-비닐알코올 공중합체를 더욱 바람직하게 사용한다.Examples of the olefinic ionomer include ethylene-acrylic acid copolymer, ethylene-methacrylic acid copolymer, propylene-acrylic acid copolymer, propylene-methacrylic acid copolymer, ethylene-vinyl alcohol copolymer, ethylene-vinylsulfonic acid copolymer, styrene Methacrylic acid copolymer, ethylene glycol-propylene glycol-ethylene glycol block copolymer, styrene-polyethylene glycol acrylate block copolymer, ethylhexyl methacrylate-polyethylene glycol acrylate block copolymer and ethylhexyl methacrylate- Hydroxyethyl methacrylate block copolymer, and an ethylene-acrylic acid copolymer or an ethylene-vinyl alcohol copolymer is more preferably used.
통상의 이오노머는 이온성이 없는 반복단위와 소량의 이온을 함유할 수 있는 반복단위로 구성된 공중합체가 일반적이며, 일종의 열가소성 탄성체로서 거동하는바, 본 발명에서는 상술한 올레핀계 이오노머가 폴리올레핀 중공사막의 표면에 코팅됨으로써 친수성으로 개질됨과 아울러 융융방사 후 연신과정에서 중공사의 신장율 향상에도 기여할 수 있다.
A typical ionomer is a copolymer composed of a repeating unit having no ionic property and a repeating unit capable of containing a small amount of ion, and behaves as a kind of thermoplastic elastomer. In the present invention, the above-mentioned olefinic ionomer is a polyolefin hollow fiber membrane It can be modified to be hydrophilic by being coated on the surface, and can also contribute to enhancement of the elongation percentage of the hollow fiber in the process of melt-spinning and drawing.
또한, 상기 올레핀계 이오노머 코팅층의 두께는 0.05~1 ㎛인 것이 바람직한바, 올레핀계 이오노머 코팅층의 두께가 0.05 ㎛미만이면 젖음성이 감소하여 물이 투과되지 않을 우려가 있고, 코팅층의 두께가 1 ㎛를 초과하면 코팅층이 표면의 기공을 막게 되어 수투과도가 저하될 수 있다.If the thickness of the olefin-based ionomer coating layer is less than 0.05 탆, the wettability may decrease and water may not be permeated. If the thickness of the coating layer is less than 1 탆 The coating layer may block pores on the surface, and water permeability may be lowered.
또한, 본 발명은 I) 폴리올레핀을 중공성형노즐을 통하여 용융방사, 냉각 및 권취하여 미연신 중공사막을 얻는 단계; II) 상기 미연신 중공사막을 100~150℃에서 1~24시간 동안 열처리한 후, 상온에서 냉연신하는 단계; III) 상기 냉연신 후, 70~140℃에서 1~60분 동안 열연신하여 폴리올레핀 중공사막을 형성하는 단계; 및 IV) 상기 폴리올레핀 중공사막의 표면에 올레핀계 이오노머를 코팅하는 단계;를 포함하는 정수기용 친수성 폴리올레핀 중공사막의 제조방법을 제공한다.
The present invention also provides a method for producing a hollow fiber membrane, comprising the steps of: I) melt-spinning, cooling and winding a polyolefin through a hollow molding nozzle to obtain an unstretched hollow fiber membrane; II) heat treating the unstretched hollow fiber membrane at 100 to 150 ° C for 1 to 24 hours, followed by cold rolling at room temperature; III) forming the polyolefin hollow fiber membrane by hot drawing at 70 to 140 ° C for 1 to 60 minutes after cold rolling; And IV) coating the surface of the polyolefin hollow fiber membrane with an olefin-based ionomer. The present invention also provides a method for producing a hydrophilic polyolefin hollow fiber membrane for a water purifier.
먼저, 상기 I) 단계에서는 폴리올레핀을 중공성형노즐을 통하여 용융방사, 냉각 및 권취하여 미연신 중공사막을 얻는바, 폴리올레핀은 상술한 바와 같이 구성한다. 그리고 용융된 폴리프로필렌의 방사온도를 150~250℃로 설정하여 균일하게 방사하며, 방사된 중공사막은 기체 또는 액체 냉매에 의하여 냉각한다. 이때, 폴리에틸렌글리콜과 같은 액체 냉매에 의하여 냉각되는 경우에는 응고액으로 인한 급속 냉각이 이루어져 중공사막 표면에서 고화현상이 너무 빠르게 진행되어 결정화도가 떨어질 수 있고, 그에 따라 기공 형성이 어렵거나 다공성이 저하될 우려가 있다. 그러므로 공기와 같은 기체 냉매를 사용하여 서서히 냉각하는 것이 급속한 고화를 방지하여 결정화도를 높게 유지할 수 있으며, 기공 형성을 용이하게 하고 다공성을 증가시킬 수 있어 바람직하다. 이어서, 냉각 고화된 중공사막의 배향성을 증가시키기 위하여 일정한 속도로 권취함으로써 미연신 중공사막을 얻는다.
First, in step I), the polyolefin is melt-spun, cooled, and wound up through a blow-molded nozzle to obtain an unstretched hollow fiber membrane. The polyolefin is constructed as described above. The spinning temperature of the molten polypropylene is set to 150 to 250 ° C. to uniformly spin the hollow fiber membrane, and the hollow fiber membrane is cooled by gas or liquid refrigerant. At this time, in the case of cooling with a liquid coolant such as polyethylene glycol, rapid cooling due to the coagulating liquid occurs, and the solidification phenomenon proceeds too fast on the surface of the hollow fiber membrane, so that the crystallization degree may be lowered, There is a concern. Therefore, it is preferable to cool slowly using a gaseous refrigerant such as air to prevent rapid solidification, to maintain the crystallinity at a high level, to facilitate pore formation and to increase porosity. Next, to increase the orientation of the hollow fiber membrane, the unfired hollow fiber membrane is obtained by winding at a constant speed.
다음으로, 상기 II) 단계에서는 상기 미연신 중공사막을 100~150℃에서 1~24시간 동안 열처리한 후, 상온에서 냉연신하는바, 열처리함으로써 중공사막 고분자 사슬의 분자 배향성을 극대화시켜 중공사막의 다공성을 더욱 증가시킨다. 또한, 상온에서 냉연신함으로써 중공사막의 표면 또는 연신 방향에 대하여 수직으로 신장된 중공사막 벽면에 다공성을 부여한다.
Next, in the step II), the unstretched hollow fiber membrane is heat-treated at 100 to 150 ° C. for 1 to 24 hours, and then cold-rolled at room temperature. As a result, the molecular orientation of the hollow fiber membrane polymer chain is maximized, Thereby further increasing the porosity. In addition, cold rolling at room temperature imparts porosity to the surface of the hollow fiber membrane or the wall of the hollow fiber membrane stretched perpendicular to the stretching direction.
이어서, 상기 III) 단계에서는 상기 II) 단계의 냉연신 후, 70~140℃에서 1~60분 동안 열연신함으로써 연신율을 미연신사 대비 200~800% 범위 내에서 조절하여 폴리올레핀 중공사막을 형성한다.
Next, in the step III), the polyolefin hollow fiber membrane is formed by cold rolling at the step II), and at a temperature of 70 to 140 ° C for 1 to 60 minutes to adjust the elongation to 200 to 800% of the unstretched fiber.
마지막으로, 상기 IV) 단계에서는 상기 I) 내지 III) 단계를 통하여 형성된 폴리올레핀 중공사막의 표면에 올레핀계 이오노머를 코팅함으로써 본 발명에 따른 친수성 폴리올레핀 중공사막을 제조한다. 이때, 코팅 공정은 딥 코팅 또는 스프레이 코팅 방법에 의하여 수행될 수 있으며, 코팅을 위한 올레핀계 이오노머 코팅 용액의 농도는 0.1 내지 5 중량% 범위로 조절하는 것이 바람직하다. 상기 올레핀계 이오노머 코팅 용액의 농도가 0.1 중량% 미만이면 표면의 친수성 개질 효과가 미미하며, 그 농도가 5 중량%를 초과하면 기공의 크기가 감소하여 수투과 성능이 저하될 수 있다.Finally, in step IV), the hydrophilic polyolefin hollow fiber membrane according to the present invention is prepared by coating an olefin-based ionomer on the surface of the polyolefin hollow fiber membrane formed through steps I) to III). At this time, the coating process may be performed by a dip coating or spray coating method, and the concentration of the olefin-based ionomer coating solution for coating is preferably adjusted in the range of 0.1 to 5 wt%. If the concentration of the olefin-based ionomer coating solution is less than 0.1 wt%, the hydrophilic modification effect of the surface is insignificant. If the concentration exceeds 5 wt%, the pore size may decrease and the water permeation performance may be deteriorated.
이하에서는 본 발명에 따른 실시예 및 비교예를 구체적으로 서술한다.
Hereinafter, examples and comparative examples according to the present invention will be described in detail.
[실시예 1] [Example 1]
용융지수(MI) 5 g/10min인 폴리프로필렌을 외경 15.0mm, 내경 8.0mm의 중공성형노즐을 이용하여 230℃에서 8.5cm/min의 방사속도로 용융방사, 상온에서 공기로 냉각 및 20m/min의 속도로 권취하여 미연신 중공사막을 얻었다. 상기 미연신 중공사막을 120℃에서 16시간 동안 열처리한 후, 상온에서 냉연신하여 미연신사 대비 연신율을 20%로 조절하였다. 상기 냉연신 후 150℃에서 30분 동안 열연신함으로써 연신율을 미연신사 대비 100%로 수행하여 폴리올레핀 중공사막을 형성하였다. 상기 폴리올레핀 중공사막을 에틸렌-비닐알코올 공중합체 2 중량% 용액에 침지 및 건조하여 코팅층(두께 0.5 ㎛)을 형성함으로써 친수성 폴리올레핀 중공사막을 제조하였다.
Polypropylene having a melt index (MI) of 5 g / 10 min was melt-spun at a spinning speed of 8.5 cm / min at a temperature of 230 캜 using a hollow-formed nozzle having an outer diameter of 15.0 mm and an inner diameter of 8.0 mm, To obtain an unstretched hollow fiber membrane. The unstretched hollow fiber membrane was heat-treated at 120 ° C for 16 hours, cold-rolled at room temperature, and adjusted to an elongation of 20% relative to unstretched filaments. After the cold rolling, the polyolefin hollow fiber membrane was formed by hot stretching at 150 ° C. for 30 minutes to obtain an elongation percentage of 100% based on the unstretched fiber. A hydrophilic polyolefin hollow fiber membrane was prepared by immersing the polyolefin hollow fiber membrane in a 2 wt% solution of ethylene-vinyl alcohol copolymer and drying to form a coating layer (thickness: 0.5 mu m).
[실시예 2][Example 2]
코팅층 형성을 위하여 에틸렌-아크릴산 공중합체 2 중량% 용액을 사용한 것을 제외하고는 실시예 1과 동일한 방법으로 친수성 폴리올레핀 중공사막을 제조하였다.
A hydrophilic polyolefin hollow fiber membrane was prepared in the same manner as in Example 1, except that a 2 wt% solution of an ethylene-acrylic acid copolymer was used to form a coating layer.
[실시예 3][Example 3]
코팅층 형성을 위하여 폴리메틸바이닐이서를 2 중량% 용액을 사용한 것을 제외하고는 실시예 1과 동일한 방법으로 친수성 폴리올레핀 중공사막을 제조하였다.
A hydrophilic polyolefin hollow fiber membrane was prepared in the same manner as in Example 1, except that a 2 wt% solution of polymethylvinylether was used to form a coating layer.
[실시예 4] [Example 4]
용융지수(MI) 0.35 g/10min인 폴리에틸렌을 사용한 것을 제외하고는 실시예 1과 동일한 방법으로 친수성 폴리올레핀 중공사막을 제조하였다. 레핀 중공사막을 제조하였다.
A hydrophilic polyolefin hollow fiber membrane was prepared in the same manner as in Example 1, except that polyethylene having a melt index (MI) of 0.35 g / 10 min was used. Lipine hollow fiber membranes were prepared.
[비교예 1][Comparative Example 1]
용융지수(MI) 15 g/10min인 폴리프로필렌을 사용한 것을 제외하고는 실시예 1과 동일한 방법으로 폴리올레핀 중공사막을 제조하였다.
A polyolefin hollow fiber membrane was prepared in the same manner as in Example 1 except that polypropylene having a melt index (MI) of 15 g / 10 min was used.
[비교예 2][Comparative Example 2]
코팅층 형성 과정을 수행하지 않은 것을 제외하고는 실시예 1과 동일한 방법으로 폴리올레핀 중공사막을 제조하였다.
A polyolefin hollow fiber membrane was prepared in the same manner as in Example 1, except that the coating layer formation process was not performed.
[비교예 3][Comparative Example 3]
코팅층 형성 과정을 수행하지 않은 것을 제외하고는 실시예 4와 동일한 방법으로 폴리올레핀 중공사막을 제조하였다.A polyolefin hollow fiber membrane was prepared in the same manner as in Example 4, except that the coating layer formation process was not performed.
도 1에는 본 발명의 실시예 1로부터 제조된 친수성 폴리프로필렌 중공사막 표면의 모폴로지를 촬영한 주사전자현미경(SEM) 이미지를 나타내었는바, 중공사막의 표면에 에틸렌-비닐알코올 공중합체의 코팅층이 균일하게 형성되어 있음을 확인할 수 있다.
FIG. 1 shows a scanning electron microscope (SEM) image of the morphology of the surface of the hydrophilic polypropylene hollow fiber membrane prepared in Example 1 of the present invention. The coating layer of the ethylene-vinyl alcohol copolymer on the surface of the hollow fiber membrane was uniform As shown in FIG.
또한, 하기 표 1에는 본 발명에 따른 상기 실시예 1 내지 4 및 비교예 1 내지 3으로부터 제조된 폴리올레핀 중공사막의 수투과도를 나타내었다. Table 1 shows the water permeability of the polyolefin hollow fiber membranes prepared in Examples 1 to 4 and Comparative Examples 1 to 3 according to the present invention.
*LMH=L/m2hr bar
* LMH = L / m 2 hr bar
위 표 1에서 보는 바와 같이, 본 발명의 실시예 1 내지 4로부터 제조된 친수성 폴리올레핀 중공사막은 비교예 1로부터 제조된 중공사막에 비하여 수투과도가 크게 높은 것을 확인할 수 있는바(비교예 2 및 3으로부터 제조된 소수성 폴리올레핀 중공사막은 수투과도가 실질적으로 0 LMH이다), 올레핀계 이오노머가 코팅된 친수성 폴리올레핀 중공사막을 구성하는 폴리올레핀의 용융지수(MI) 및 코팅 여부가 수투과도에 영향을 미치는 중요한 인자임을 알 수 있다.As shown in Table 1, the hydrophilic polyolefin hollow fiber membranes prepared in Examples 1 to 4 of the present invention had significantly higher water permeability than the hollow fiber membranes prepared in Comparative Example 1 (Comparative Examples 2 and 3 (MI) of the polyolefin constituting the hydrophilic polyolefin hollow fiber membrane coated with the olefin ionomer and an important factor affecting the water permeability of the hydrophilic polyolefin hollow fiber membrane prepared from the hydrophobic polyolefin hollow fiber membrane .
그러므로 본 발명에 따라 제조된 친수성 폴리올레핀 중공사막은 종래 정수기용 중공사막에 비하여 수투과도가 크게 향상되고 기계적 강도도 우수하여 정수기의 중공사막 필터로서 유용하다.Therefore, the hydrophilic polyolefin hollow fiber membrane produced according to the present invention is significantly useful as a hollow fiber membrane filter of a water purifier because it greatly improves the water permeability and mechanical strength compared to the conventional hollow fiber membrane for water purifier.
Claims (8)
II) 상기 미연신 중공사막을 100~150℃에서 1~24시간 동안 열처리한 후, 상온에서 냉연신하는 단계;
III) 상기 냉연신 후, 150℃에서 30분 동안 열연신함으로써 연신율을 미연신사 대비 100%로 수행하여 폴리프로필렌 중공사막을 형성하는 단계; 및
IV) 상기 폴리프로필렌 중공사막의 표면에 에틸렌-아크릴산 공중합체를 코팅함으로써 두께가 0.05~1 ㎛인 코팅층을 형성하는 단계;를 포함하는 정수기용 친수성 폴리프로필렌 중공사막의 제조방법.I) melt-spinning the polypropylene having a melt index (MI) of 5 g / 10 min through a blow-molding nozzle at 150 to 250 ° C, cooling it with air at room temperature to obtain an unstretched hollow fiber membrane;
II) heat treating the unstretched hollow fiber membrane at 100 to 150 ° C for 1 to 24 hours, followed by cold rolling at room temperature;
III) forming the polypropylene hollow fiber membrane by performing hot drawing at 150 ° C for 30 minutes after the cold rolling, and performing an elongation of 100% with respect to the unstretched filament; And
IV) forming a coating layer having a thickness of 0.05 to 1 탆 by coating the surface of the polypropylene hollow fiber membrane with an ethylene-acrylic acid copolymer to form a hydrophilic polypropylene hollow fiber membrane for a water purifier.
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