CN101890308B - External compression type hollow fiber ultrafiltration membrane and preparation method - Google Patents
External compression type hollow fiber ultrafiltration membrane and preparation method Download PDFInfo
- Publication number
- CN101890308B CN101890308B CN2010101531673A CN201010153167A CN101890308B CN 101890308 B CN101890308 B CN 101890308B CN 2010101531673 A CN2010101531673 A CN 2010101531673A CN 201010153167 A CN201010153167 A CN 201010153167A CN 101890308 B CN101890308 B CN 101890308B
- Authority
- CN
- China
- Prior art keywords
- temperature
- described preparation
- membrane
- preparation
- water
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000012528 membrane Substances 0.000 title claims abstract description 47
- 238000002360 preparation method Methods 0.000 title claims abstract description 24
- 239000012510 hollow fiber Substances 0.000 title claims abstract description 12
- 238000000108 ultra-filtration Methods 0.000 title abstract description 3
- 238000007906 compression Methods 0.000 title description 4
- 230000006835 compression Effects 0.000 title 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract description 29
- 239000003085 diluting agent Substances 0.000 claims abstract description 20
- 229920000642 polymer Polymers 0.000 claims abstract description 17
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims abstract description 15
- KMZHZAAOEWVPSE-UHFFFAOYSA-N 2,3-dihydroxypropyl acetate Chemical compound CC(=O)OCC(O)CO KMZHZAAOEWVPSE-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229920002981 polyvinylidene fluoride Polymers 0.000 claims abstract description 8
- 239000002033 PVDF binder Substances 0.000 claims abstract 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 28
- 239000000835 fiber Substances 0.000 claims description 22
- 239000000203 mixture Substances 0.000 claims description 21
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 14
- 239000000463 material Substances 0.000 claims description 11
- 238000001816 cooling Methods 0.000 claims description 10
- 235000012489 doughnuts Nutrition 0.000 claims description 10
- 239000012809 cooling fluid Substances 0.000 claims description 9
- -1 polyoxyethylene Polymers 0.000 claims description 9
- 238000002156 mixing Methods 0.000 claims description 8
- 239000002994 raw material Substances 0.000 claims description 8
- 239000007788 liquid Substances 0.000 claims description 7
- 229910052757 nitrogen Inorganic materials 0.000 claims description 6
- 238000005096 rolling process Methods 0.000 claims description 5
- 239000002826 coolant Substances 0.000 claims description 4
- 238000002386 leaching Methods 0.000 claims description 4
- 238000005469 granulation Methods 0.000 claims description 3
- 230000003179 granulation Effects 0.000 claims description 3
- 238000001223 reverse osmosis Methods 0.000 claims description 3
- 238000009987 spinning Methods 0.000 claims description 3
- 238000003756 stirring Methods 0.000 claims description 3
- 229910001873 dinitrogen Inorganic materials 0.000 claims description 2
- 238000001035 drying Methods 0.000 claims description 2
- 239000000155 melt Substances 0.000 claims description 2
- 125000003003 spiro group Chemical group 0.000 claims description 2
- 238000005303 weighing Methods 0.000 claims description 2
- 238000000034 method Methods 0.000 abstract description 16
- 238000001471 micro-filtration Methods 0.000 abstract description 8
- 230000008569 process Effects 0.000 abstract description 6
- 239000000126 substance Substances 0.000 abstract description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract 1
- 238000005516 engineering process Methods 0.000 description 9
- 238000012360 testing method Methods 0.000 description 8
- 230000004907 flux Effects 0.000 description 5
- 239000011148 porous material Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 4
- 239000002351 wastewater Substances 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 3
- 239000010865 sewage Substances 0.000 description 3
- 238000005266 casting Methods 0.000 description 2
- 239000006184 cosolvent Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- 238000005191 phase separation Methods 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 230000010148 water-pollination Effects 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical class CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- XKMRRTOUMJRJIA-UHFFFAOYSA-N ammonia nh3 Chemical compound N.N XKMRRTOUMJRJIA-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000003373 anti-fouling effect Effects 0.000 description 1
- 239000012296 anti-solvent Substances 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000002210 biocatalytic effect Effects 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 238000000280 densification Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 230000029087 digestion Effects 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000010842 industrial wastewater Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000036284 oxygen consumption Effects 0.000 description 1
- 239000002957 persistent organic pollutant Substances 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
Images
Abstract
The invention relates to a polyvinylidene fluoride porous hollow fiber membrane and a preparation method thereof. The membrane comprises the following components in percentage by mass: 25 to 48 percent of polyvinylidene fluoride (PVDF) serving as a first polymer P1, 0 to 5 percent of polyethylene oxide (PEO) serving as a second polymer P2, 31 to 44 percent of glyceryl acetate serving as a first diluent D1, and 18 to 34 percent of glycol serving as a second diluent D2. The PVDF hollow fiber ultrafiltration membrane and the PVDF hollow fiber microfiltration membrane which are prepared by adopting the method have excellent chemical stability, and are the hollow fiber membrane with pollution resistance and high strength; and the method can provide high performance membrane products for MBR process.
Description
Technical field
The present invention relates to a kind of Kynoar (PVDF) porous hollow fiber membrane and method for making thereof, especially relate to a kind of external-compression type Kynoar (PVDF) porous hollow fiber membrane and method for making thereof.
Background technology
Membrane biological reactor process (MBR) is a kind of novel, sewage disposal technology efficiently, and it can realize separating of biocatalytic reaction and water and degradation material simultaneously, and water resource is regenerated, and realizes the reuse water standard.Be the waste water advanced processing and the regeneration new technology of advanced, efficient and low energy consumption in the present age.Wherein preparing intensity height, antifouling property good, milipore filter and micro-filtration membrane cheaply, is the core technology of membrane biological reactor process.But at present most ofs commercially surpass, the micro-filtration membrane effect is all undesirable, can't satisfy industrial requirement.On the other hand, super at present, the most employing non-solvents of micro-filtration membrane cause the phase separation method preparation, and the film of being made comprises the big cavity structure of finger-like mostly, membrane aperture skewness, intensity difference, use easy fracture of wire in sewage, membrane lifetime is short, is unsuitable for using in membrane biological reactor process.
Summary of the invention
The objective of the invention is to propose a kind of Kynoar porous hollow fiber membrane and method for making thereof that is suitable in membrane biological reactor process, using.
Kynoar porous hollow fiber membrane provided by the invention, its system composition of film and content thereof be by percentage to the quality:
First polymer P
1: Kynoar (PVDF) 25～48%
Second polymer P
2: polyoxyethylene (PEO) 0～5%
The first diluent D
1: glyceryl acetate 31～44%
The second diluent D
2: ethylene glycol 18～34%.
Preferably, wherein said Kynoar (PVDF) weight average molecular weight is 300000, and described polyoxyethylene (PEO) weight average molecular weight is 20000.
Preferably, wherein the mass ratio of each composition is:
P
2/P
1＝0～0.12，
D
1/D
2＝1.2/1～1.8/1，
P/ (P+D)=(25～48) %, wherein: P=P
1+ P
2, D=D
1+ D
2
Preferred, wherein the mass ratio of each composition is:
Wherein said P
2/ P
1=0.05～0.08,
Wherein said D
1/ D
2=1.3/1～1.4/1,
Wherein said P/ (P+D)=(35～40) %.
On the other hand, the present invention also provides a kind of preparation method of described hollow-fibre membrane, comprises the following steps:
(1) preliminary treatment of polymeric material
Kynoar, polyoxyethylene are carried out drying in dryer, bake out temperature is 50～80 ℃;
(2) preparation of system film blend raw material
With Kynoar P
1With polyoxyethylene P
2, glyceryl acetate D
1With ethylene glycol D
2After the weighing, be placed on earlier in the stirred tank in proportion, under 130～155 ℃ temperature, carry out stirring and dissolving, mixing time is 15～25 hours, speed of agitator is 80～120 rev/mins, will dissolve system film Polymer Solution cooling granulation in air uniformly, obtains the blend raw material;
(3) hollow-fibre membrane extrudes, is shaped
(4) diluent leaching
The doughnut intermediate of making is immersed in the reverse osmosis water, remove the diluent mixture in the film, water temperature is 25～45 ℃, and leaching time is 2～6 hours;
(5) dry
The hollow-fibre membrane of making at room temperature dried promptly get the doughnut membrane product.
Preferably, wherein the temperature in the step (1) is 60～70 ℃.
Preferably, wherein the mixing time described in the step (2) is 22～24 hours, and described speed of agitator is 90～100 rev/mins.
Preferably, wherein step (3) may further comprise the steps:
(3-1) will melt extrude in the above-mentioned blend raw material adding double screw extruder;
The melt blended material of (3-2) extruding is extruded from the doughnut annular die through filter and spinning pump, forms the as-spun fibre of hollow;
(3-3) above-mentioned as-spun fibre is lowered the temperature in air, cooling curing in cooling fluid through the winder rolling, is made the doughnut intermediate then.
Preferred, wherein the charging rate of raw material is 8kg/h in the step (3-1), and extruder is divided into 8 sections along the spiro rod length direction and heats, and the temperature range of 8 sections is 110～155 ℃, and screw speed is 120 rev/mins.
Preferred, wherein the external diameter of annular die single hole is 5.5 millimeters (mm) in the step (3-2), and internal diameter is 5.0 millimeters, and temperature is 140～150 ℃, and the annular die centre bore feeds nitrogen, and nitrogen gas pressure is 20～50 millimeter of water (mmH
2O), preferred nitrogen pressure is 30～40 millimeter of water (mmH
2O).
Preferred, wherein in the step (3-3) above-mentioned as-spun fibre in being 5～25 ℃ air, temperature is lowered the temperature, and preferred air themperature is 10～25 ℃, and winder rolling speed is 10～15m/min, and cooling fluid is glyceryl acetate C
1, ethylene glycol C
2And water C
3Three's mixed liquor, coolant temperature are 5～40 ℃, and preferred coolant temperature is 10～20 ℃.
Preferred, wherein export to the air gap of cooling off liquid level and remain 10～25 centimetres from the mouth mould, preferred the air gap is 15～20 centimetres.
Preferably, wherein the ratio of three's mixing is (mass ratio): (C
1+ C
2)/C
3=10/9～4/1, C
1/ C
2=1.4/1～1.8/1.
Preferred, wherein the ratio of three's mixing is (mass ratio): (C
1+ C
2)/C
3=4/3～3/1, C
1/ C
2=1.4/1～1.6/1.
Preferably, wherein the water temperature described in the step (4) is 25～35 ℃, and the time is 3～4 hours.
The Kynoar (PVDF) that the present invention adopts has outstanding anti-solvent, acid and alkali-resistance, resistance to oxidation, characteristic such as weather-proof, excellent hear resistance and toughness are arranged, particularly the fluorine element in the material has stronger negative polarity, makes PVDF be difficult for being adsorbed with organic pollutants, show good anti pollution property, is the preferred material of MBR technology.
Yet because PVDF material hydrophobicity is strong, the surface can be low, and hydrone is had repulsive interaction, and the present invention adopts hydrophilic high molecular material blend with it, thereby improves the hydrophily of pvdf membrane effectively.
On this basis, the present invention also proposes a kind of new mixed diluent system, this system is made up of two component mixed solvents, one of them component is the solvent or the cosolvent of polymer, another component is the non-solvent of polymer, by adjusting the different proportion between the two in the mixed diluent, come interactional power between telomerized polymer and the diluent, and then the phase-separated state of change polymer/diluent system, reach the purpose of regulation and control membrane pore structure, prepare the film of required three-dimensional net structure.
On this basis, the present invention adopts the mixed liquor of diluent and water as cooling fluid, by changing the composition and the temperature of cooling fluid, regulate the aperture on film surface and the size of percent opening, super, the micro-filtration membrane of the PVDF that preparation has the hole density gradient improves film pollutant is held back characteristic and the stifled ability of anti-soil.
On the other hand, preparation method provided by the invention, utilized the principle of " high-temperature digestion, low temperature phase-splitting ", with polymer and diluent at high temperature mixed dissolution become uniform casting film solution, again solution is made tabular, tubulose and hollow fiber after, through cooling, cooling, casting solution system generation liquid-liquid or solid-liquid are separated, after polymeric system solidifies, again the diluent extraction is removed, promptly obtain porous diffusion barrier.This method is extensive to the adaptability of high polymer material, not only is suitable for conventional high polymer, and it is poor even because highly crystalline also to be suitable for dissolved separating property, undissolvable polymer under common normal temperature.Because film-forming temperature is higher relatively, the concentration of corresponding filming polymer is also higher relatively, can avoid occurring non-solvent and cause the big cavity structure of the sort of finger-like that phase separation method is made, it is even to make pore structure, the three-dimensional net structure of Guan Tonging highly, therefore the film strength height can adapt to the requirement of MBR technology.Super, the micro-filtration membrane of the PVDF doughnut that adopts the present invention to prepare has excellent chemical stability, and antipollution, the hollow-fibre membrane that intensity is high can provide high performance film product for MBR technology.
In addition, diluent is non-water-soluble in traditional filming technology, needs to adopt alcohol, ketone, ester class organic solvent as extractant after film is shaped, and this technology is except own expense height with an organic solvent, also to add the cost that reclaims extractant, can't avoid the discharging of organic pollution.Among the present invention since mixed diluent system in two components be water miscible, so just can adopt water as come together diluent (cosolvent) in the membrane of extractant, can avoid the trouble that adopts organic solvent to bring, also can reduce the manufacturing cost of film as extractant.
Hollow-fibre membrane external diameter of the present invention is 1.1～1.3 millimeters, wall thickness is 290～310 nanometers, membrane pore structure is three-dimensional interpenetrating polymer network structure (seeing accompanying drawing 1,2), the film section is asymmetric, film outmost surface aperture minimum, the densification of outer wall edge hole, the aperture is less, the aperture increases gradually from outside to inside, and inner surface aperture maximum is a kind of super, micro-filtration membrane with density gradient pores section structure.Super, micro-filtration membrane of the present invention has good chemically-resistant cleaning and hydrophily, and intensity height, big, the good toughness of flux have good contamination resistance, are adapted at most using among the MBR.City domestic sewage, industrial wastewater can be carried out advanced treating, water reuse water standard in reaching.Compare with traditional Wastewater Treated by Activated Sludge Process waste water, treatment effeciency improves more than 3 times, and effluent quality is good, and chemical oxygen consumption (COC) in the waste water (COD) clearance is greater than 98%, ammonia-nitrogen removal efficiency height, the treatment facility compactness, take up an area of less, automaticity height, convenient operation and management.
Description of drawings
Fig. 1 is near the film cross-section structure of outer surface
Fig. 2 intermediate coat cross-section structure
The specific embodiment
For a more detailed description below in conjunction with embodiment to the present invention, but described embodiment is not construed as limiting the invention.
Embodiment 1
The quality percentage is that 40% PVDF oven dry resin and mass percent are the polymer blend that 3.2% polyoxyethylene oven dry resin is formed, join in the mixed solvent of glyceryl acetate and ethylene glycol composition, wherein the quality percentage of glyceryl acetate is 33.1% (wt), and the quality percentage of ethylene glycol is 23.7%.Said mixture is joined in the stirred tank, is to carry out stirring and dissolving after 24 hours under 120 rev/mins of kind conditions at 155 ℃ temperature, rotating speed, and cooling granulation in air obtains blended material.Charging rate with 8kg/h joins preprepared blend composition in the double screw extruder.The temperature in extruder 1-8 district is respectively 110 ℃, 125 ℃, 140 ℃, 150 ℃, 150 ℃, 155 ℃, 155 ℃, 150 ℃, and screw speed is 120 rev/mins.After mixed material melt extrudes in dual-screw-stem machine, enter four hole annular dies by filter and spinning pump and extrude, make the hollow as-spun fibre, a mouthful mould single hole external diameter is 5.5mm, and internal diameter is 5mm, and temperature is 150 ℃, and it is 40mmH that a mouthful mould centre bore feeds pressure
2The N of O
2Gas.As-spun fibre is in temperature is 25 ℃ air, and idling stopping distance (the air gap) is 25cm, enters into the cooling fluid cooling curing, with the speed rolling of 15m/min.Wherein contain 25% water in the cooling fluid, 28.8% ethylene glycol, 46.2% glyceryl acetate, the temperature of cooling fluid is 30 ℃.Preformed hollow-fibre membrane leaches and at room temperature dries after 4 hours in 30 ℃ reverse osmosis water, makes doughnut membrane product of the present invention.By scanning electronic microscope observation, the inierpeneirating network structure of the section of film, asymmetric milipore filter, film surface average pore size is 47 nanometers (nm), and the fiber external diameter is 1.3 millimeters (mm), and wall thickness is 309 microns (μ m).Under temperature was 25 ℃, 0.1MPa pressure, pure water flux was 500L/m
2H, tensile strength of fiber are 7.8MPa, elongation at break 110%.
Provide main preparation process condition and the film properties of embodiment of the invention 2-5 below in conjunction with table 1, but the content of each composition of the present invention is not limited to listed numerical value in this table, for a person skilled in the art, fully can be in table rationally summarize and reasoning on the basis of listed number range, and of particular note, although listed file names with some other parameter in the table 1, this this parameter condition is described as necessary condition.For the present invention, the content of core is to improve the film formula of liquid, and therefore, other parameters that list file names with in the table 1 are just in order to provide in more detail about technical information of the present invention, all be preferred condition, described as necessary condition of the present invention.
Table 1: the formulation ratio of embodiment 2-5, main preparation process condition and film properties
Wherein, film properties data relevant in the table 1 are hollow-fibre membrane is cooled off brittle failure in liquid nitrogen after, and the use stereomicroscope is taken a picture to the section of described film and measured, and method is as follows:
(1) Micro-Structure Analysis of film
Sample is made in film brittle failure in liquid nitrogen, sample is fixed on the sample platform, under the voltage of 30KV, adopt SEM (QuanTa 200FEG) observation film section and surface texture.
(2) film-strength test
Film is made the sample silk, and two ends reinforce with medical proof fabric.On universal testing machine, stretch in (GT-TS-2000, GOTECHCO, Taiwan) hot strength of test membrane silk and elongation at break.
(3) pure water flux of film test
Testing arrangement is by external-compression type ultrafilter, N
2Gas cylinder, vacuum tank are formed, and hollow-fibre membrane is packaged into specimen with epoxide-resin glue, and the employing temperature is 25 ℃ a deionized water, tests under the pressure of 0.1MPa.
Pure water flux is defined as the pure water quality that sees through at following unit interval of above-mentioned test condition, elementary membrane area.
That is: J=W/AT
Wherein, J is pure water flux (kg/m
2H), A is the external surface area (m of film
2), W is the permeable amount (kg) of film, T is testing time (h).
(4) mensuration of the external diameter of hollow-fibre membrane, internal diameter and wall thickness
Any corresponding improvement of carrying out on basis of the present invention does not all break away from thought of the present invention, all falls into the scope of protection of the invention.
Claims (15)
1. Kynoar porous hollow fiber membrane, the composition of its system film and content thereof be by percentage to the quality:
First polymer P
1: Kynoar (PVDF) 25～48%
Second polymer P
2: polyoxyethylene (PEO) 0～5%
The first diluent D
1: glyceryl acetate 31～44%
The second diluent D
2: ethylene glycol 18～34%;
The mass ratio of each composition further is:
P
2/P
1＝0.05～0.08，
D
1/D
2＝1.3/1～1.4/1，
P/ (P+D)=(35～40) %, wherein: P=P
1+ P
2, D=D
1+ D
2
Described Kynoar (PVDF) weight average molecular weight is 300000, and described polyoxyethylene (PEO) weight average molecular weight is 20000.
2. the preparation method of the described hollow-fibre membrane of claim 1 comprises the following steps:
(1) preliminary treatment of polymeric material
Kynoar, polyoxyethylene are carried out drying in dryer, bake out temperature is 50～80 ℃;
(2) preparation of system film blend raw material
With Kynoar P
1With polyoxyethylene P
2, glyceryl acetate D
1With ethylene glycol D
2After the weighing, be placed on earlier in the stirred tank in proportion, under 130～155 ℃ temperature, carry out stirring and dissolving, mixing time is 15～25 hours, speed of agitator is 80～120 rev/mins, will dissolve system film Polymer Solution cooling granulation in air uniformly, obtains the blend raw material;
(3) hollow-fibre membrane extrudes, is shaped
(4) diluent leaching
The doughnut intermediate of making is immersed in the reverse osmosis water, remove the diluent mixture in the film, water temperature is 25～45 ℃, and leaching time is 2～6 hours;
(5) dry
The hollow-fibre membrane of making at room temperature dried promptly get the doughnut membrane product.
3. the described preparation method of claim 2, wherein the temperature in the step (1) is 60～70 ℃.
4. the described preparation method of claim 2, wherein the mixing time described in the step (2) is 22～24 hours, described speed of agitator is 90～100 rev/mins.
5. the described preparation method of claim 2, wherein step (3) may further comprise the steps:
(3-1) will melt extrude in the above-mentioned blend raw material adding double screw extruder;
The melt blended material of (3-2) extruding is extruded from the doughnut annular die through filter and spinning pump, forms the as-spun fibre of hollow;
(3-3) above-mentioned as-spun fibre is lowered the temperature in air, cooling curing in cooling fluid through the winder rolling, is made the doughnut intermediate then.
6. the described preparation method of claim 5, wherein the charging rate of raw material is 8kg/h in the step (3-1), and extruder is divided into 8 sections along the spiro rod length direction and heats, and the temperature range of 8 sections is 110～155 ℃, and screw speed is 120 rev/mins.
7. the described preparation method of claim 5, wherein the external diameter of annular die single hole is 5.5 millimeters (mm) in the step (3-2), and internal diameter is 5.0 millimeters, and temperature is 140～150 ℃, the annular die centre bore feeds nitrogen, and nitrogen gas pressure is 20～50 millimeter of water (mmH
2O).
8. the described preparation method of claim 7, wherein said nitrogen pressure is 30～40 millimeter of water (mmH
2O).
9. the described preparation method of claim 5 wherein lowers the temperature above-mentioned as-spun fibre in the step (3-3) in temperature is 5～25 ℃ air, winder rolling speed is 10～15m/min, and cooling fluid is glyceryl acetate C
1, ethylene glycol C
2And water C
3Three's mixed liquor, coolant temperature are 5～40 ℃.
10. the described preparation method of claim 9, wherein said air themperature is 10～25 ℃, described coolant temperature is 10～20 ℃.
11. the described preparation method of claim 5 wherein exports to the air gap of cooling off liquid level from the mouth mould and remains 10～25 centimetres.
12. the described preparation method of claim 11, wherein said the air gap is 15～20 centimetres.
13. the described preparation method of claim 9, wherein the ratio of three's mixing is (mass ratio): (C
1+ C
2)/C
3=10/9～4/1, C
1/ C
2=1.4/1～1.8/1.
14. the described preparation method of claim 13, wherein the ratio of three's mixing is (mass ratio): (C
1+ C
2)/C
3=4/3～3/1, C
1/ C
2=1.4/1～1.6/1.
15. the described preparation method of claim 2, wherein the water temperature described in the step (4) is 25～35 ℃, and the time is 3～4 hours.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2010101531673A CN101890308B (en) | 2010-04-23 | 2010-04-23 | External compression type hollow fiber ultrafiltration membrane and preparation method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2010101531673A CN101890308B (en) | 2010-04-23 | 2010-04-23 | External compression type hollow fiber ultrafiltration membrane and preparation method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101890308A CN101890308A (en) | 2010-11-24 |
| CN101890308B true CN101890308B (en) | 2011-11-23 |
Family
ID=43099747
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2010101531673A Expired - Fee Related CN101890308B (en) | 2010-04-23 | 2010-04-23 | External compression type hollow fiber ultrafiltration membrane and preparation method |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN101890308B (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110605032A (en) * | 2018-06-16 | 2019-12-24 | 苏州五颗星特种超滤膜科技有限公司 | Preparation method of finishing type hollow fiber membrane |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999059707A1 (en) * | 1998-05-18 | 1999-11-25 | Usf Filtration And Separations Group Inc. | Highly porous polyvinylidene difluoride membranes |
| JP2003210954A (en) * | 2002-01-24 | 2003-07-29 | Toray Ind Inc | Method of manufacturing hollow fiber membrane and hollow fiber membrane |
| CN1481272A (en) * | 2001-10-04 | 2004-03-10 | ������������ʽ���� | Hollow fiber film and method for prodn thereof |
| CN1899678A (en) * | 2005-07-19 | 2007-01-24 | 天津工业大学 | Method for producing hollow fiber film |
| CN101370572A (en) * | 2006-01-11 | 2009-02-18 | 东洋纺织株式会社 | Polyvinylidene fluoride hollow yarn type microporous film and process for production of the same |
-
2010
- 2010-04-23 CN CN2010101531673A patent/CN101890308B/en not_active Expired - Fee Related
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999059707A1 (en) * | 1998-05-18 | 1999-11-25 | Usf Filtration And Separations Group Inc. | Highly porous polyvinylidene difluoride membranes |
| CN1481272A (en) * | 2001-10-04 | 2004-03-10 | ������������ʽ���� | Hollow fiber film and method for prodn thereof |
| JP2003210954A (en) * | 2002-01-24 | 2003-07-29 | Toray Ind Inc | Method of manufacturing hollow fiber membrane and hollow fiber membrane |
| CN1899678A (en) * | 2005-07-19 | 2007-01-24 | 天津工业大学 | Method for producing hollow fiber film |
| CN101370572A (en) * | 2006-01-11 | 2009-02-18 | 东洋纺织株式会社 | Polyvinylidene fluoride hollow yarn type microporous film and process for production of the same |
Also Published As
| Publication number | Publication date |
|---|---|
| CN101890308A (en) | 2010-11-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| WO2013073828A1 (en) | Hydrophilic polyvinylidene fluoride-based hollow-fiber separation membrane, and method for manufacturing same | |
| CN101890303B (en) | Hollow fibrous membrane with asymmetrical structure and preparation method thereof | |
| CN101890304B (en) | Porous membrane with three-dimensional interpenetrating polymer network and preparation method | |
| CN102527250B (en) | Hollow fibrous membrane and preparation method thereof | |
| CN104607064A (en) | Method for preparing polyvinylidene fluoride-graphene oxide composite hollow fiber membrane | |
| CN103143268B (en) | The preparation method of polyvinylidene fluoride/polyurethane/polyvinyl chloride blend hollow fiber separation membrane | |
| CN101890309B (en) | Method for preparing hollow fiber membranes by using thermally induced phase separation (TIPS) process | |
| CN101890312B (en) | Hydrophilic PVDF ultrafiltration membrane and preparation method | |
| WO2010082437A1 (en) | Vinylidene fluoride resin hollow fiber porous membrane and process for producing same | |
| KR20140046638A (en) | Method for manufacturing asymmetric hollow fiber membrane and asymmetric hollow fiber membrane manufactured using the same | |
| CN101879417B (en) | Hollow fiber membrane containing PMMA (Polymethyl Methacrylate) and preparation method thereof | |
| CN101874991B (en) | PVDF ultra-filtration membrane taking ethyl orthosilicate as additive and preparation method | |
| CN101890311B (en) | Method for preparing asymmetric polyvinylidene fluoride (PVDF) ultrafiltration membrane | |
| CN103272494B (en) | Preparation method of polyvinylidene fluoride alloy membrane for wastewater treatment during high-salinity food processing | |
| CN1242025A (en) | Melt-spun polysulfone semipermeable membranes and methods for making the same | |
| CN101890310B (en) | Porous membrane using acetic acid-2-ethoxyl ethyl ester and polyethylene glycol as diluents and preparation method | |
| KR20160081612A (en) | PVDF porous hollow fiber membrane and the preparing method thereof | |
| CN101920173B (en) | Ultrafiltration membrane using ethylene glycol carbonic ester and diethylene glycol as diluent and manufacturing method thereof | |
| CN101890308B (en) | External compression type hollow fiber ultrafiltration membrane and preparation method | |
| CN101890313B (en) | Porous membrane using mixed diluent system and preparation method | |
| CN101890307B (en) | Hollow-fiber membrane with density gradient pores and preparation method | |
| CN101874992B (en) | PVDF (Polyvinylidene Fluoride) alloy film containing two hydrophilic high polymers and preparation method | |
| CN103638833B (en) | A kind of preparation method of the large flux hollow fiber membranes for drink water purifying | |
| CN103638828B (en) | Be used for the preparation method of the ultralow pressure polyvinylidene fluoride alloy membrane of drinking water treatment | |
| CN103638830A (en) | Preparation method of hot-method polyvinylidene fluoride hollow fiber membrane for drinking water treatment |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| PP01 | Preservation of patent right | ||
| PP01 | Preservation of patent right |
Effective date of registration: 20170428 Granted publication date: 20111123 |
|
| PD01 | Discharge of preservation of patent | ||
| PD01 | Discharge of preservation of patent |
Date of cancellation: 20180428 Granted publication date: 20111123 |
|
| PP01 | Preservation of patent right | ||
| PP01 | Preservation of patent right |
Effective date of registration: 20180428 Granted publication date: 20111123 |
|
| PD01 | Discharge of preservation of patent | ||
| PD01 | Discharge of preservation of patent |
Date of cancellation: 20210428 Granted publication date: 20111123 |
|
| CF01 | Termination of patent right due to non-payment of annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20111123 Termination date: 20200423 |