CN1063235A - The preparation of hypertonicity polysulfone hollow fibre milipore filter - Google Patents
The preparation of hypertonicity polysulfone hollow fibre milipore filter Download PDFInfo
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- CN1063235A CN1063235A CN91106007A CN91106007A CN1063235A CN 1063235 A CN1063235 A CN 1063235A CN 91106007 A CN91106007 A CN 91106007A CN 91106007 A CN91106007 A CN 91106007A CN 1063235 A CN1063235 A CN 1063235A
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Abstract
A kind of preparation technology of hypertonicity polysulfone hollow fibre milipore filter comprises the preparation liquid of employing polysulfones-solvent-nonsolvent-salt-surfactant penton system preparation and does two main processes of spray-wet spinning spining technology.Utilize the technology of the present invention can prepare the hollow fiber ultrafiltration membrane with different molecular weight cut offs, they have the high purity water permeability.Prepared filter membrane is assembled into ultrafilter can be in the production of thymic peptide, and enzyme preparations such as human's purifying, carbohydrase and urokinase concentrate and reach separating, concentrating and sterilization or ultra-pure water production application of other biochemical product, have the wide range of industrial applications prospect.
Description
The present invention relates to a kind of preparation technology of polymer ultrafiltration membrane, specifically provide the process that a kind of preparation has high osmosis energy hollow fiber ultrafiltration membrane.
Develop rapidly along with bionic since milipore filter and isolation technics thereof have can be at normal pressure, normal temperature or low temperature is operation down, no phase transformation can keep the pH value of filtrate, and can concentrate simultaneously and characteristics such as purifying, is replacing the traditional handicraft process gradually.Be widely used in enzyme preparation, vaccine, medicine, the separation of gene biological goods concentrates and purifying, and the application aspect bioenzyme film reactor also makes significant progress.Hollow fiber membrane ultrafiltration device becomes a kind of ultrafilter of extensive employing with characteristics such as its film loading density are big, and the development of hollow fiber ultrafiltration membrane is its key problem.Hollow-fibre membrane normally adopts the gel method preparation, issue the process that looks transforms based on Polymer Solution in the precipitating reagent effect, because the shaping of hollow-fibre membrane is the viscosity oneself support by self, thereby the viscosity lower limit of spinning film liquid is very limited, and in precipitation process, the exchange of solvent and precipitating reagent all takes place in the surfaces externally and internally of film, and interacts and influence the final structure of film.Membrane structure depends primarily on two aspect effects: 1, the epuilibrium thermodynamics character of film making solution and precipitation system; 2, in the film forming process solvent and precipitating reagent exchange rate to the film forming procedure effect of kinetics.In the preparation process of actual membrane, then be mainly the preparation liquid system of the suitable hollow fiber ultrafiltration membrane of apolegamy and the process conditions that the film preparation process adopts.The reported in literature system film slurries system for preparing hollow fiber ultrafiltration membrane was generally ternary system in the past, and the most representative single skin structural membrane of making as U.S. Amicon company is based on polysulfones-solvent-salt (zinc chloride) ternary system.And two cortex construction films of company of Japanese Asahi Chemical Industry manufacturing, adopt with polysulfones-solvent-electrolyte ternary system.
The purpose of this invention is to provide a kind of technology of new preparation hollow fiber ultrafiltration membrane, this film has porous and high pore volume, promptly has high water permeation performance.Simultaneously, by controlling diaphragm surface holes warp and membrane structure form, thereby produce the filter membrane that stayed performance in various years.
The present invention is the hollow fiber ultrafiltration membrane that makes the high water-permeability energy, adopts with polysulfones-solvent-nonsolvent-salt-surfactant penton system preparation liquid system that is made into.Because non-solvent, the adding of salt and surfactant makes system film slurry viscosity improve, thereby can prepare the film liquid than low polymer content, and the viscosity requirement of necessity when guaranteeing spinning, more easily obtains the filter membrane that porous is held.And, also improved the hydrophily of film and soaked into the angle, thereby improved water permeability owing to add surfactant.
It is the product of η=0.5～0.7 that used polysulfones (Psf) can adopt inherent viscosity; Solvent can adopt dimethylacetylamide (DMAC), dimethyl formamide (DMF), dimethyl sulfoxide (DMSO) (DMSO) or N-methyl arsenic pyrrolidone (NMP); Non-solvent is a deionized water; Salt can be lithium nitrate, lithium chloride or magnesium perchlorate; Last surfactant can adopt TritonX-100, tween T-80, Triton X-100 or other emulsifying agent.In the preparation liquid that above-mentioned penton is, its percentage by weight is:
Polysulfones: 15～25%; Solvent: 70～82.5%; Non-solvent, salt and surfactant: 2.5～5%; And non-solvent, salt and surfactant are pressed the percentage by weight preparation again: non-solvent, 90.5～95.5%; Salt, 4～8%; Surfactant, 0.5～1.5%.The detailed process of preparing slurries according to the above ratio is: get quantitative polysulfones and add stirred tank, take by weighing quantitative non-solvent (deionized water) again, pour in the quantitative solvent after salt and surfactant stir, pour into after the stirring in the stirred tank material is stirred well, carry out vacuum defoamation, the static film slurries that make more than 5 hours.For guaranteeing that the slurries each component fully is mixed, in the stirred tank whipping process, should keep 50～60 ℃ of constant temperature, with 80～120 rev/mins of process speed, stir and be advisable in 12～20 hours.
Preparation technology of the present invention, except that above-mentioned selection raw material preparation preparation liquid, another preparation main points are exactly to adopt a suitable filming technology condition.The preparation of filter membrane adopt to be done spray-wet spinning spining technology and is made among the present invention.Its technological process as shown in Figure 1.As shown in Figure 1 in the spinning membrane system process chart: 1, batch can; 2, filter; 3, pump; 4, shower nozzle; 5, coagulate groove outward; 6,8, cylinder; 7, washing trough; 9, the interior agent jar that coagulates.Shower nozzle 4 has concentric ring formula structure as shown in Figure 2, and 10, interior pipe; 11, outer tube; 12, outer tube wall.Preparation liquid in the batch can 1 filters the back through filter 2 and squeezes into shower nozzle 4 by pump 3, sprays from interannular outer tube 11 cracks, garden, makes the nascent state fiber form hollow and coagulate medium in the injection of interior pipe, coagulates the coagulating bath freezing film of groove 5 outside injecting then.Different proportionings according to preparation liquid, suitably regulate spinning operating condition: nozzle structure and size, nozzle temperature, inside and outside medium and the temperature of coagulating, shower nozzle is to solidifying the molten distance of asking, pump feeding, interior supply and the draw speed etc. of coagulating, can change the pore size and the structural form of film within the specific limits, thereby obtain to have the hollow fiber ultrafiltration membrane of different molecular cutting performance.Suitable process conditions is: feed temperature (nozzle temperature): 5～25 ℃; The inside and outside medium that coagulates: the aqueous solution of 0～50% solvent; The inside and outside temperature of coagulating: 5～25 ℃; Spray is apart from coagulating molten distance: 10～20mm.Can make milipore filter by above-mentioned condition, can under drying regime, preserve, also must protect processing film for making the gained film.The protection processing of adopting among the present invention is a method of utilizing the aqueous solution of 15～30% glycerine and 0.5～1.5% surfactant once to soak into tunica fibrosa.After handling like this, make hollow fiber ultrafiltration membrane and in the kept dry process, keep its high osmosis energy fully, and when the assembling hollow fiber membrane ultrafiltration device, guarantee hollow fibre filament and adhering with epoxy resin material good bonding performance.Below by example preparation technology of the present invention is described further.
The preparation of example 1 hollow fiber filter membrane
Press column weight amount percentage and take by weighing raw material, Psf, 18.6%; DMAC, 78.8%, H
2O,
Press column weight amount percentage and take by weighing raw material, Psf, 18.6%; DMAC, 78.8%, H
2O, LiNO
3With T-80 2.6% preparation system film slurries, its process is: press earlier 94%H
2O, 5%LiNO
3, after mixing it, the ratio of 1%T-80 stirs among the adding DMAC, and pour in the stirred tank and stir with Psf, placed 12 hours.Whipping temp is 50 ℃, and speed is 120 rev/mins, and the preparation liquid for preparing is pressed into and carries out vacuum defoamation in the batch can 1.Its shower nozzle is of a size of d
Outward=1.0mm, d
In=0.7mm, d
The hole=0.45mm, slurries are from the ejection of shower nozzle annular space, and temperature is controlled at 5 ℃, injects outer the bath with fixed attention then and solidifies, and again through rinsing bowl, becomes silk with 9 meters/bundling speed coiling boundling.Interior lime set is gone into the nascent state fibrillar center to form hollow with infusion, and interior lime set is the 30%DMAC aqueous solution, and outer coagulating is water, and coagulating temperature outward is 5 ℃, and the rinsing bowl temperature is 25 ℃.The hollow-fibre membrane that is spun into is assembled into hollow fiber membrane ultrafiltration device BS in the time of can be in dry state after the guarantor obtains liquid and handles
3
Example 2, the preparation 2 of hollow fiber filter membrane
Press column weight amount percentage and take by weighing raw material: Psf, 23%; DMAC, 74%; H
2O, LiCl and T-80,3% preparation system film slurries are pressed example 1 described preparation process, only replace LiNo with LiCl
3, nozzle temperature is controlled at 25 ℃, and coagulating temperature outward is 20 ℃, and other condition adopts same guarantor to obtain processing and form ultrafiltration BS1 with the example 1 identical hollow-fibre membrane that makes.
Example 3,4, the preparation 3,4 of hollow fiber filter membrane
Press example 1 described preparation process and condition, but grout coordinate ratio is adopted following column weight amount percentage: Psf, 16.5%; DMSO80.1%H
2, LiNo
3And T-80,2.6% is made into system film slurries shower nozzle is of a size of d
Outward=1.1mm, d
In=0.8mm, d
The hole=0.5mm, other is identical with example 1, repeats example 1 process and makes hollow-fibre membrane, is assembled into ultrafilter BS5.
Press Psf, 15.5%; NMP81.1%; H
2O, LiNO
3And T-80,2.6% is made into system film slurries, adopts above-mentioned other five example 1 of shower nozzle chi head identical, repeats example 1 process and makes hollow-fibre membrane, is assembled into ultrafiltration BS10.
Example 5, the hollow fiber filter membrane performance test
10～20 of the hollow fiber filter membrane that above-mentioned example 1～4 is made are packed in φ 10 * 300mm glass tube, and two ends seal with epoxy resin adhesive, are assembled into small-sized ultrafilter BS3, BS1, BS5, BS10, measure the rejection and the water permeation performance of film.Its cutoff performance such as table 1, water permeation performance such as table 2.
The table 1 BS series typical solute retention characteristic of hollow fiber filter membrane (holding back characteristic %)
| Solute | Molecular weight | BS1 | BS3 | BS5 | BS10 |
| Bacitracin | 1.400 | ||||
| Cromoci | 12.400 | 95 | |||
| Ribalgilase | 13.700 | 61 | 16 | 0 | |
| Chymotrypsin | 25.000 | 85 | 67 | 0 | |
| The egg protein enzyme | 45.000 | 98 | 98 | ||
| Bovine serum albumin | 67.000 | 98 | 98 | 98 | 77 |
| γ one globulin | 156.000 | 96 |
Table 2 BS series hollow fiber filter membrane pure water permeability performance
| The film model | Molecular weight cut off | 25 ℃ of PWP liters/hour rice 0.1MPa |
| BS1 | 10.000 | 60～80 |
| BS3 | 30.000 | 160～210 |
| BS5 | 50.000 | 250～300 |
| BS10 | 100.000 | 560～600 |
By table 1,2 results, but the BS series hollow fiber filter membrane molecular weight cut off of the invention described above preparation is 10,000,30,000,50,000,100,000, has difference and holds back characteristic.Made filter membrane has pure water permeability energy preferably simultaneously.Utilize ESEM further to study the structure of BS series hollow fiber filter membrane, its section is double finger-like pore structure, and inside and outside all have a dense layer surface, and the test burst pressure has mechanical strength preferably at 1.0～1.3MPa.
Example 6, the BS hollow fiber ultrafiltration membrane is made with extra care thymic peptide
Utilize the hollow fiber filter membrane and the refining thymic peptide experiment of BS1 of example 2 preparations.Without the refining thymic peptide suspension of ultrafiltration, through regulating pH value generally near 6.0, total protein content is about 10mg/ml, a lot of molecular weight is wherein arranged greater than 10,000 foreign protein and bacterium.The results are shown in Table 3 through the refining gained of BS hollow fiber ultrafiltration membrane ultrafiltration.
| Project | Sample volume (ml) | Last (min) | VO/V1 | Cp(mg/ml) | Product quality * |
| 1 | 500 | 20 | 3.8 | 5.40 | Qualified |
| 2 | 1630 | 72 | 16 | 5.85 | Qualified |
| 3 | 2900 | 155 | 29 | 5.31 | Qualified |
| 4 | 3800 | 216 | 38 | 7.28 | Qualified |
* thermal source detects-" biological products pyrogen test rules "
Bacteria Culture-" biological products sterility test rules "
Content of peptides-" forint-phenol law "
Below all by Chinese Pharmacopoeia version method test in 1985.
V0 is the sample initial volume in the table 3, and V1 is that sample is made with extra care concentrated volume when stopping, and Cp is penetrating fluid (purified product) mean value concentration.These table data are by BS1 type inner pressed polysulfone hollow fiber ultrafiltration membrane system gained.Assembly effective film area is 0.1m
2, operation element pressure is 0.1MPa, the sample liquid temperature is less than 10 ℃.Result of the test shows that the BS1 film not only reaches the purpose of refining thymic peptide, but also can remove thermal source and bacterium.
Example 7 BS hollow fiber filter membrane purifying are gone into the alpha-interferon experiment
Utilize example 1 preparation hollow fiber filter membrane and BS3 purifying to go into the alpha-interferon experiment, through interferon inducers be induced into blood leukocytes and produce go into the alpha-interferon elaboration, its pH value is about 6.0.The material liquid temperature is tired generally 2 * 10 below 10 ℃
3Repeated ultrafiltration experiment has been done repeatedly with this sample by unit.BS Hollow Fiber Ultrafiltration products obtained therefrom and experimental result are compared through animal experiment, Bacteria Culture, thermal source mensuration and ultraviolet spectrometer detection and electrophoresis apparatus analysis, the results are shown in down tabulation 4:
The unconcerned purifying people of table 4 BS Hollow Fiber Ultrafiltration ɑ-interferon experiment
| Project | Sample volume (ml) | Last (min) | ＊ CR | Friendship valency unit/ml | Thermal source and Bacteria Detection |
| 1 | 1000 | 28 | 6 | ＞500 | Qualified |
| 2 | 1850 | 68 | 11 | ＞8000 | Qualified |
| 3 | 4260 | 155 | 28 | ＞8000 | Qualified |
| 4 | 1500 | 53 | 10 | ＞10000 | Qualified |
* V
CRVolume cycles of concentration, film model are BS, and operating pressure is 0.1MPa
The * thermal source detects-" biological products pyrogen test rules "
Bacteria Culture-" biological products sterility test rules "
Can see from above-mentioned example, utilize the invention provides existing system preparation liquid prescription the slurries of modulating and filming technology technology, can prepare hollow fiber ultrafiltration membrane with different molecular weight cut offs, they have the high purity water permeability.Prepared filter membrane is assembled into the production of ultrafilter in thymic peptide, human's classification, the separating of terminal purifying and sterilization and other bioid goods, concentrate and sterilization aspect or ultra-pure water production in have wide application prospect.
Claims (3)
1, a kind of preparation method of hypertonicity polysulfone hollow fibre milipore filter, it comprises selects the preparation liquid prescription and does two major parts of spray-wet spinning spinning membrane system technology, it is characterized in that preparation liquid is to adopt polysulfones-solvent-nonsolvent-salt-surfactant penton system preparation, wherein can to adopt inherent viscosity be the product of η=0.5～0.7 to polysulfones (PSf); Solvent can adopt dimethylacetylamide, dimethyl formamide, dimethyl sulfoxide (DMSO) or N-methyl arsenic pyrrolidone; Non-solvent is a deionized water, and salt can be lithium nitrate, lithium chloride or magnesium perchlorate; Surfactant can adopt TritonX-100, tween T-80, Triton X-100 or other emulsifying agent; Spinning membrane system technology suitable process conditions is: feed temperature (nozzle temperature): 5～25 ℃; The inside and outside medium that coagulates: the aqueous solution of 0～50% solvent; The inside and outside temperature of coagulating: 5～25 ℃; Shower nozzle is apart from bathing distance: 10～20mm with fixed attention.
2,, it is characterized in that the five body constituents that is adopted is that the preparation liquid prescription is (percentage by weight): polysulfones: 15～25% according to the described preparation method of claim 1; Solvent: 70～82.5%; Non-solvent, salt and surfactant: 2.5～5%; And non-solvent, salt and surfactant are pressed the percentage by weight preparation: non-solvent: 90.5～95.5%; Salt: 4～8%; Surface-active: 0.5～1.5%.
3, according to the described preparation method of claim 1, it is characterized in that can protecting and obtain processing obtained filter membrane, promptly utilize the processing method of the solution immersion tunica fibrosa of 15～30% glycerine and 0.5～1.5 surface-active.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 91106007 CN1029773C (en) | 1991-01-09 | 1991-01-09 | Preparation of hypertonic polysulfone hollow fibred ultrafiltering film |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 91106007 CN1029773C (en) | 1991-01-09 | 1991-01-09 | Preparation of hypertonic polysulfone hollow fibred ultrafiltering film |
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| Publication Number | Publication Date |
|---|---|
| CN1063235A true CN1063235A (en) | 1992-08-05 |
| CN1029773C CN1029773C (en) | 1995-09-20 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 91106007 Expired - Lifetime CN1029773C (en) | 1991-01-09 | 1991-01-09 | Preparation of hypertonic polysulfone hollow fibred ultrafiltering film |
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Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1053387C (en) * | 1994-03-15 | 2000-06-14 | 中国科学院大连化学物理研究所 | Method for preparation of improved complex film with coating |
| CN100352903C (en) * | 1995-06-07 | 2007-12-05 | 鲍德温·格拉菲克系统有限公司 | Process for producing cleaning agent with high viscosity |
| CN105879717A (en) * | 2016-02-15 | 2016-08-24 | 山东招金膜天股份有限公司 | Method for preparing high-flux polyether-sulfone hollow-fiber ultra-filtration membrane |
| CN107158976A (en) * | 2017-06-27 | 2017-09-15 | 彭雅龙 | A kind of milipore filter handled for the Organic substance in water that gives up and preparation method thereof |
| CN109984998A (en) * | 2019-05-23 | 2019-07-09 | 山东和兴药业有限公司 | Injection omeprazole sodium, preparation method and be the application caused by preventing regurgitation of gastric juice in aspiration pneumonia in indication |
| CN110479121A (en) * | 2019-07-30 | 2019-11-22 | 三达膜科技（厦门）有限公司 | A kind of preparation method of polyether sulfone/thermo plastic polyurethane alastic body alloy inner support hollow membrane |
-
1991
- 1991-01-09 CN CN 91106007 patent/CN1029773C/en not_active Expired - Lifetime
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1053387C (en) * | 1994-03-15 | 2000-06-14 | 中国科学院大连化学物理研究所 | Method for preparation of improved complex film with coating |
| CN100352903C (en) * | 1995-06-07 | 2007-12-05 | 鲍德温·格拉菲克系统有限公司 | Process for producing cleaning agent with high viscosity |
| CN105879717A (en) * | 2016-02-15 | 2016-08-24 | 山东招金膜天股份有限公司 | Method for preparing high-flux polyether-sulfone hollow-fiber ultra-filtration membrane |
| CN107158976A (en) * | 2017-06-27 | 2017-09-15 | 彭雅龙 | A kind of milipore filter handled for the Organic substance in water that gives up and preparation method thereof |
| CN109984998A (en) * | 2019-05-23 | 2019-07-09 | 山东和兴药业有限公司 | Injection omeprazole sodium, preparation method and be the application caused by preventing regurgitation of gastric juice in aspiration pneumonia in indication |
| CN110479121A (en) * | 2019-07-30 | 2019-11-22 | 三达膜科技（厦门）有限公司 | A kind of preparation method of polyether sulfone/thermo plastic polyurethane alastic body alloy inner support hollow membrane |
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| Publication number | Publication date |
|---|---|
| CN1029773C (en) | 1995-09-20 |
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Inventor after: Jiang Chengzhang Inventor after: Zhang Hengshan Inventor after: Lin Yizheng Inventor after: Qin Jianjun Inventor after: Wang Zhengjian Inventor after: Tian Yan Inventor after: Song Yuguan Inventor after: Yang Daling Inventor after: Jiang Guirong Inventor after: Dai Zhihe Inventor before: Jiang Chengzhang Inventor before: Lin Yifeng Inventor before: Qin Jianjun Inventor before: Wang Zhengjian Inventor before: Tian Yan Inventor before: Yang Daling Inventor before: Jiang Guirong Inventor before: Dai Zhihe Inventor before: Zhang Hengshan |
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Free format text: CORRECT: INVENTOR; FROM: JIANG CHENGZHANG; LIN YIFENG; QIN JIANJUN; WANG ZHENGJIAN; TIAN YAN; YANG DALING; JIANG GUIRONG; DAI ZHIHE; ZHANG HENGSHAN TO: JIANG CHENGZHANG; LIN YIZHENG; QIN JIANJUN; WANG ZHENGJIAN; TIAN YAN; SONG YUGUAN; YANG DALING; JIANG GUIRONG; DAI ZHIHE; ZHANG HENGSHAN |
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Effective date of registration: 20090220 Address after: Liaoning province Dalian City High-tech Park Qixianling Torch Road No. 28 Patentee after: Tianbang National Engineering Research Center of Membrane Technology, Co., Ltd. Address before: No. 161, Zhongshan Road, Liaoning, Dalian Patentee before: Dalian Institute of Chemical Physics, Chinese Academy of Sciences |
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Owner name: TIANBANG MEMBRANE TECHNOLOGY COUNTRY ENGINEERING R Free format text: FORMER OWNER: DALIAN INST OF CHEMICOPHYSICS, CHINESE ACADEMY OF SCIENCES Effective date: 20090220 |
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Expiration termination date: 20110109 Granted publication date: 19950920 |