WO2021237381A1 - 一种稀土改性聚醚砜超滤膜的制备方法 - Google Patents
一种稀土改性聚醚砜超滤膜的制备方法 Download PDFInfo
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- 239000012528 membrane Substances 0.000 title claims abstract description 22
- 239000004695 Polyether sulfone Substances 0.000 title claims abstract description 18
- 229920006393 polyether sulfone Polymers 0.000 title claims abstract description 18
- 238000000108 ultra-filtration Methods 0.000 title claims abstract description 16
- 238000000034 method Methods 0.000 title abstract description 8
- 239000000243 solution Substances 0.000 claims abstract description 55
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 30
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims abstract description 25
- 229910052761 rare earth metal Inorganic materials 0.000 claims abstract description 22
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000011521 glass Substances 0.000 claims abstract description 13
- 238000003756 stirring Methods 0.000 claims abstract description 13
- 239000008367 deionised water Substances 0.000 claims abstract description 12
- 229910021641 deionized water Inorganic materials 0.000 claims abstract description 12
- 150000002910 rare earth metals Chemical class 0.000 claims abstract description 12
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims abstract description 10
- 239000011259 mixed solution Substances 0.000 claims abstract description 9
- 238000010438 heat treatment Methods 0.000 claims abstract description 7
- MHABMANUFPZXEB-UHFFFAOYSA-N O-demethyl-aloesaponarin I Natural products O=C1C2=CC=CC(O)=C2C(=O)C2=C1C=C(O)C(C(O)=O)=C2C MHABMANUFPZXEB-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229920002565 Polyethylene Glycol 400 Polymers 0.000 claims abstract description 6
- XAYGUHUYDMLJJV-UHFFFAOYSA-Z decaazanium;dioxido(dioxo)tungsten;hydron;trioxotungsten Chemical compound [H+].[H+].[NH4+].[NH4+].[NH4+].[NH4+].[NH4+].[NH4+].[NH4+].[NH4+].[NH4+].[NH4+].O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.[O-][W]([O-])(=O)=O.[O-][W]([O-])(=O)=O.[O-][W]([O-])(=O)=O.[O-][W]([O-])(=O)=O.[O-][W]([O-])(=O)=O.[O-][W]([O-])(=O)=O XAYGUHUYDMLJJV-UHFFFAOYSA-Z 0.000 claims abstract description 6
- 238000001035 drying Methods 0.000 claims abstract description 6
- FYDKNKUEBJQCCN-UHFFFAOYSA-N lanthanum(3+);trinitrate Chemical compound [La+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O FYDKNKUEBJQCCN-UHFFFAOYSA-N 0.000 claims abstract description 6
- JLFNLZLINWHATN-UHFFFAOYSA-N pentaethylene glycol Chemical compound OCCOCCOCCOCCOCCO JLFNLZLINWHATN-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000003361 porogen Substances 0.000 claims abstract description 6
- 238000001291 vacuum drying Methods 0.000 claims abstract description 6
- 229910000027 potassium carbonate Inorganic materials 0.000 claims abstract description 5
- 238000002360 preparation method Methods 0.000 claims description 18
- -1 rare earth alkali metal Chemical class 0.000 claims description 9
- PBYZMCDFOULPGH-UHFFFAOYSA-N tungstate Chemical compound [O-][W]([O-])(=O)=O PBYZMCDFOULPGH-UHFFFAOYSA-N 0.000 claims description 7
- 229910052783 alkali metal Inorganic materials 0.000 claims description 6
- 150000001768 cations Chemical class 0.000 claims description 6
- 229910052751 metal Inorganic materials 0.000 claims description 6
- 239000002184 metal Substances 0.000 claims description 6
- 239000002905 metal composite material Substances 0.000 claims description 6
- 229920000642 polymer Polymers 0.000 claims description 6
- 239000002994 raw material Substances 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 2
- 230000000844 anti-bacterial effect Effects 0.000 abstract description 4
- 230000004907 flux Effects 0.000 abstract description 3
- 238000007790 scraping Methods 0.000 abstract 1
- 239000004033 plastic Substances 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 239000004753 textile Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 3
- 238000009285 membrane fouling Methods 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 2
- 238000000614 phase inversion technique Methods 0.000 description 2
- 239000002861 polymer material Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 1
- 229920012266 Poly(ether sulfone) PES Polymers 0.000 description 1
- HYXRNUXQERMPQH-UHFFFAOYSA-N [K].[La] Chemical compound [K].[La] HYXRNUXQERMPQH-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 239000000022 bacteriostatic agent Substances 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- QNEFNFIKZWUAEQ-UHFFFAOYSA-N carbonic acid;potassium Chemical compound [K].OC(O)=O QNEFNFIKZWUAEQ-UHFFFAOYSA-N 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 210000000170 cell membrane Anatomy 0.000 description 1
- 210000002421 cell wall Anatomy 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 230000003834 intracellular effect Effects 0.000 description 1
- 238000013178 mathematical model Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 238000001223 reverse osmosis Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 229910021642 ultra pure water Inorganic materials 0.000 description 1
- 239000012498 ultrapure water Substances 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 238000004065 wastewater treatment Methods 0.000 description 1
Classifications
-
- 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
-
- 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
- B01D69/02—Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor characterised by their properties
-
- 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
- B01D69/06—Flat membranes
Definitions
- the invention relates to a preparation method of a rare earth modified polyethersulfone ultrafiltration membrane.
- the Pechini method uses the polyester effect of the ⁇ -hydroxy carboxyl group between the metal chelate and the polyhydric alcohol to form a compound. Due to the chemical reaction between cations and organic acids, they are uniformly dispersed in the polymer resin, which can ensure the mixing at the atomic level, and generate uniform, single-phase ultra-fine oxide powder at a relatively low temperature.
- Ultrafiltration is a chemical separation technology that has emerged since the end of the 20th century. Since the 1960s, membrane separation technology has entered the industrial field and has been widely used.
- the phase inversion method is a relatively simple membrane preparation method with simple process, convenient operation and wide range of uses. It can be used to prepare various membranes for reverse osmosis, ultrafiltration, and gas separation.
- Ultrafiltration membranes are mainly used in the field of water treatment. In recent years, they have been widely used in wastewater treatment, ultrapure water preparation, medicine, and food. With technological progress, the performance of ultrafiltration membranes will surely be improved and strengthened. Bring greater contributions in various fields.
- Polyethersulfone (PES) is a high polymer with excellent properties. Its glass transition temperature reaches 225°C. It has good mechanical strength, acid and alkali resistance, heat resistance and chemical stability. It can be used as a raw material. Preparation of ultrafiltration membranes with excellent performance.
- Rare earth plays an important role in the plastic industry and textile industry. It is mainly used as a stabilizer and plastic auxiliary in the plastic industry. In actual use, it enhances product performance and reduces pollution. It improves fiber affinity and strength in the textile industry. And save costs. It can be used as a coupling agent to improve the unique electronic layer structure of polymer materials and rare earth elements (the outermost and sub-outer electrons are easy to lose), and form rare earth ions with different valences, making the rare earths have active coordination properties. It acts with bacterial cell wall, cytoplasmic membrane and intracellular DNA to inhibit the proliferation and growth of bacteria, so that the rare earth has an antibacterial effect. According to the current research status, rare earth compounds have broad application space as bacteriostatic agents. At present, relevant research has shown that rare earth compounds have unique effects on the preparation and use performance of polymer materials.
- the purpose of the present invention is to provide a method for preparing rare earth modified polyethersulfone ultrafiltration membrane.
- a preparation method of rare earth modified polyethersulfone ultrafiltration membrane including the following steps: Dissolve 7-9 parts of lanthanum nitrate in 25-35 parts of ionized water to form solution A, and mix 4-6 parts of ammonium paratungstate and 9-11 parts of carbonic acid Potassium is dissolved in 25-35 parts of deionized water to form solution B, 15-25 parts of citric acid is dissolved in 30-40 parts of deionized water to form solution C; half of solution C is added to solution A, the other half is added to solution B, and Stir separately for 15-25 minutes to form a stable complex between the metal cation and citric acid; slowly add solution A to solution B, and at the same time add 8-12 parts of ethylene glycol, and then heat the mixed solution to 65-75°C and Stir continuously for 2-4h to obtain sol; transfer the obtained sol to a constant temperature blast drying box, heat it at 65-75°C for 25-27h, and then obtain rare earth alkali metal composite tungstate gel through a vacuum drying
- the mixed solution is heated to 70° C. and continuously stirred for 3 hours to obtain a sol.
- heating is performed at 70° C. for 26 hours.
- the preparation method it is allowed to stand for 6 hours to defoam.
- the glass plate is stably put into ultrafiltration water at 25° C. to form a film naturally.
- the method is simple, fast and easy to operate.
- the pure water flux of the polyethersulfone flat membrane after the addition of rare earths is significantly increased, the mechanical properties are also improved, and it is more stable, and has a significant antibacterial effect.
- a preparation method of rare earth modified polyethersulfone ultrafiltration membrane comprising the following steps: dissolving 8 parts of lanthanum nitrate in 30 parts of ionized water to form solution A, and dissolving 5 parts of ammonium paratungstate and 10 parts of potassium carbonate in 30 parts of deionized water
- solution B dissolve 20 parts of citric acid in 35 parts of deionized water to form solution C
- solution C dissolve 20 parts of citric acid in 35 parts of deionized water to form solution C
- solution C dissolve half of solution C to solution A, and the other half to solution B, and stir for 20 minutes to make the metal cation and citric acid form a stable complex
- the rare earth alkali metal composite tungstate gel was obtained through a vacuum drying oven; 30
- a preparation method of rare earth modified polyethersulfone ultrafiltration membrane comprising the steps of dissolving 7 parts of lanthanum nitrate in 25 parts of ionized water to form solution A, and dissolving 4 parts of ammonium paratungstate and 9 parts of potassium carbonate in 25 parts of deionized water
- solution B dissolve 15 parts of citric acid in 30 parts of deionized water to form solution C
- solution C dissolve 15 parts of citric acid in 30 parts of deionized water to form solution C
- solution C dissolve 15 parts of solution C to solution A, and the other half to solution B, and stir for 15 minutes to make the metal cation and citric acid form a stable complex
- the rare earth alkali metal composite tungstate gel is obtained in a vacuum drying oven
- a preparation method of rare earth modified polyethersulfone ultrafiltration membrane including the following steps: dissolving 9 parts of lanthanum nitrate in 35 parts of ionized water to form solution A, and dissolving 6 parts of ammonium paratungstate and 11 parts of potassium carbonate in 35 parts of deionized water
- solution B dissolve 25 parts of citric acid in 40 parts of deionized water to form solution C
- solution C dissolve 25 parts of solution C to solution A, and the other half to solution B, and stir for 25 minutes to make the metal cation and citric acid form a stable complex
- the rare earth alkali metal composite tungstate gel was obtained through a vacuum drying oven; 35 parts of dry PES, 7 parts of porogen PEG400 and 9 parts of the gel prepared above
- the method is simple, fast and easy to operate.
- the pure water flux of the polyethersulfone flat membrane after the addition of rare earths is significantly increased, the mechanical properties are also improved, and it is more stable, and has a significant antibacterial effect.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Separation Using Semi-Permeable Membranes (AREA)
Abstract
一种稀土改性聚醚砜超滤膜的制备方法,步骤如下:将硝酸镧溶于去离子水中得溶液A,将仲钨酸铵和碳酸钾溶于去离子水中得溶液B,将柠檬酸溶于去离子水中得溶液C;将一半的溶液C加入溶液A,另一半加入溶液B,分别搅拌;将溶液A缓慢加入溶液B中,并同时加入乙二醇,加热到65-75℃搅拌2-4h得溶胶;将所得溶胶转移至鼓风恒温干燥箱加热25-27h,后经真空干燥箱得凝胶;将干燥的PES、致孔剂PEG400和上述制备的凝胶在DMAC中搅拌溶解,静置脱泡,在玻璃板上用刮刀刮膜,然后放入超滤水中自然成膜,即得;加入稀土后的聚醚砜平板膜纯水通量有明显的升高,力学性能也提升了,且具有显著的抑菌作用。
Description
本发明涉及一种稀土改性聚醚砜超滤膜的制备方法。
Pechini法是利用金属螯合物之间的α-羟基羧基和多羟基醇的聚酯作用,形成化合物。由于阳离子与有机酸发生化学反应而均匀地分散在聚合物树脂中,能保证原子水平的混合,在相对较低的温度下生成均一、单相的超细氧化物粉末。超滤是从20世纪末以来崛起的化工分离技术。20世纪60年代起,膜分离技术进入了工业领域且被广泛应用。相转化法是一种较为简单的制膜方法,其工艺简单,操作方便,用途广泛,可用来制备各种反渗透、超滤、气体分离所用的膜。目前大多数的工业用膜都是用相转化法制成的。超滤膜主要运用在水处理领域,近年来在废水处理、超纯水制备、医药、食品等方面的应用越来越广,随着技术进步,超滤膜的性能必将得到改进加强,为各领域带来更大的贡献。聚醚砜(PES)是一种具有优良性能的高聚物,其玻璃化温度达到225℃,有着较好的机械强度、耐酸碱性、耐热性和化学稳定性等优势,可作原材料制备性能优良的超滤膜。在膜污染机理的理论研究中,己有许多研究者根据自己实验提出各种不同经验或半经验的膜污染数学模型,但尚无广泛适用的方程,因为影响膜污染的因素太多。本研究以电镜下观测产品的洁净度与菌落来定义污染程度。稀土(rare earth)有着“工业维生素”之称,是目前极为重要的战略资源。钨酸镧钾属于稀土碱金属复合钨酸盐,是一种具有优良性质的稀土掺杂基质材料。最早在冶金工业中加入稀土体现出了多种优异性能。近些年来,稀土在轻工纺织领域的应用有了长足发展,提高了纺织、塑料、建材等行业的产品性能与经济效益。
稀土在塑料工业及纺织工业中,有着举足轻重的地位,在塑料工业中主要用作稳定剂与塑料助剂,实际运用中增强了产品性能、减少了污染,在纺织工业中改善纤维亲和力、提升强度以及节约成本。可作为偶联剂,改善高分子材料与稀土元素具有的独特电子层结构(最外层和次外层电子易失去),形成不同价态的稀土离子,使得稀土具有活泼的配位性,可与细菌细胞壁、细胞质膜及细胞内DNA作用,对细菌的增殖生长起抑制作用,从而使稀土具有抗菌作用。根据现有研究状况,稀土化合物做抑菌剂有着广阔的应用空间。目前有关研究已经表明,稀土化合物对高分子材料的制备和使用性能等方面有着独特的功效。
发明内容
本发明的目的在于提供一种稀土改性聚醚砜超滤膜的制备方法。
本发明通过下面技术方案实现:
一种稀土改性聚醚砜超滤膜的制备方法,包括如下步骤:将7-9份硝酸镧溶于25-35份离子水中形成溶液A,将4-6份仲钨酸铵和9-11份碳酸钾溶于25-35份去离子水中形成溶液B,将15-25份柠檬酸溶于30-40份去离子水中形成溶液C;将一半的溶液C加入溶液A,另一半加入溶液B,并分别搅拌15-25min,使金属阳离子与柠檬酸形成稳定的络合物;将溶液A缓慢加入溶液B中,并同时加入8-12份乙二醇,然后将混合溶液加热到65-75℃并持续搅拌2-4h得溶胶;将所得溶胶转移至鼓风恒温干燥箱,在65-75℃下加热25-27h,后经真空干燥箱得稀土碱金属复合钨酸盐凝胶;将25-35份干燥的PES、5-7份致孔剂PEG400和7-9份上述制备的凝胶在74-76℃的DMAC中搅拌溶解,直至聚合物溶液变得均匀透明,静置脱泡5-7h,在玻璃板上用间宽0.2mm的刮刀刮膜,然后将玻璃板平稳放入20-30℃超滤水中自然成膜,即得;各原料均为重量份。
优选地,所述的制备方法中,将混合溶液加热到70℃并持续搅拌3h得溶胶。
优选地,所述的制备方法中,在70℃下加热26h。
优选地,所述的制备方法中,静置脱泡6h。
优选地,所述的制备方法中,将玻璃板平稳放入25℃超滤水中自然成膜。
本发明技术效果:
该方法简便、快捷、易操作,加入稀土后的聚醚砜平板膜纯水通量有明显的升高,力学性能也提升了,且更加稳定,而且具有显著的抑菌作用。
下面结合实施例具体介绍本发明的实质性内容。
实施例1
一种稀土改性聚醚砜超滤膜的制备方法,包括如下步骤:将8份硝酸镧溶于30份离子水中形成溶液A,将5份仲钨酸铵和10份碳酸钾溶于30份去离子水中形成溶液B,将20份柠檬酸溶于35份去离子水中形成溶液C;将一半的溶液C加入溶液A,另一半加入溶液B,并分别搅拌20min,使金属阳离子与柠檬酸形成稳定的络合物;将溶液A缓慢加入溶液B中,并同时加入10份乙二醇,然后将混合溶液加热到70℃并持续搅拌3h得溶胶;将所得溶胶转移至鼓风恒温干燥箱,在70℃下加热26h,后经真空干燥箱得稀土碱金属复合钨酸盐凝胶;将30份干燥的PES、6份致孔剂PEG400和8份上述制备的凝胶在75℃的DMAC中搅拌溶解,直至聚合物溶液变得均匀透明,静置脱泡6h,在玻璃板上用间宽0.2mm的刮刀刮膜,然后将玻璃板平稳放入25℃超滤水中自然成膜,即得;各原料均为重量份。
实施例2
一种稀土改性聚醚砜超滤膜的制备方法,包括如下步骤:将7份硝酸镧溶于25份离子水 中形成溶液A,将4份仲钨酸铵和9份碳酸钾溶于25份去离子水中形成溶液B,将15份柠檬酸溶于30份去离子水中形成溶液C;将一半的溶液C加入溶液A,另一半加入溶液B,并分别搅拌15min,使金属阳离子与柠檬酸形成稳定的络合物;将溶液A缓慢加入溶液B中,并同时加入8份乙二醇,然后将混合溶液加热到65℃并持续搅拌2h得溶胶;将所得溶胶转移至鼓风恒温干燥箱,在65℃下加热25h,后经真空干燥箱得稀土碱金属复合钨酸盐凝胶;将25份干燥的PES、5份致孔剂PEG400和7份上述制备的凝胶在74℃的DMAC中搅拌溶解,直至聚合物溶液变得均匀透明,静置脱泡5h,在玻璃板上用间宽0.2mm的刮刀刮膜,然后将玻璃板平稳放入20℃超滤水中自然成膜,即得;各原料均为重量份。
实施例3
一种稀土改性聚醚砜超滤膜的制备方法,包括如下步骤:将9份硝酸镧溶于35份离子水中形成溶液A,将6份仲钨酸铵和11份碳酸钾溶于35份去离子水中形成溶液B,将25份柠檬酸溶于40份去离子水中形成溶液C;将一半的溶液C加入溶液A,另一半加入溶液B,并分别搅拌25min,使金属阳离子与柠檬酸形成稳定的络合物;将溶液A缓慢加入溶液B中,并同时加入12份乙二醇,然后将混合溶液加热到75℃并持续搅拌4h得溶胶;将所得溶胶转移至鼓风恒温干燥箱,在75℃下加热27h,后经真空干燥箱得稀土碱金属复合钨酸盐凝胶;将35份干燥的PES、7份致孔剂PEG400和9份上述制备的凝胶在76℃的DMAC中搅拌溶解,直至聚合物溶液变得均匀透明,静置脱泡7h,在玻璃板上用间宽0.2mm的刮刀刮膜,然后将玻璃板平稳放入30℃超滤水中自然成膜,即得;各原料均为重量份。
该方法简便、快捷、易操作,加入稀土后的聚醚砜平板膜纯水通量有明显的升高,力学性能也提升了,且更加稳定,而且具有显著的抑菌作用。
Claims (5)
- 一种稀土改性聚醚砜超滤膜的制备方法,其特征在于包括如下步骤:将7-9份硝酸镧溶于25-35份离子水中形成溶液A,将4-6份仲钨酸铵和9-11份碳酸钾溶于25-35份去离子水中形成溶液B,将15-25份柠檬酸溶于30-40份去离子水中形成溶液C;将一半的溶液C加入溶液A,另一半加入溶液B,并分别搅拌15-25min,使金属阳离子与柠檬酸形成稳定的络合物;将溶液A缓慢加入溶液B中,并同时加入8-12份乙二醇,然后将混合溶液加热到65-75℃并持续搅拌2-4h得溶胶;将所得溶胶转移至鼓风恒温干燥箱,在65-75℃下加热25-27h,后经真空干燥箱得稀土碱金属复合钨酸盐凝胶;将25-35份干燥的PES、5-7份致孔剂PEG400和7-9份上述制备的凝胶在74-76℃的DMAC中搅拌溶解,直至聚合物溶液变得均匀透明,静置脱泡5-7h,在玻璃板上用间宽0.2mm的刮刀刮膜,然后将玻璃板平稳放入20-30℃超滤水中自然成膜,即得;各原料均为重量份。
- 根据权利要求1所述的制备方法,其特征在于:将混合溶液加热到70℃并持续搅拌3h得溶胶。
- 根据权利要求1所述的制备方法,其特征在于:在70℃下加热26h。
- 根据权利要求1所述的制备方法,其特征在于:静置脱泡6h。
- 根据权利要求1所述的制备方法,其特征在于:将玻璃板平稳放入25℃超滤水中自然成膜。
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