CN110180410A - A kind of adjustable blended ultrafiltration membrane in aperture - Google Patents

A kind of adjustable blended ultrafiltration membrane in aperture Download PDF

Info

Publication number
CN110180410A
CN110180410A CN201910410007.3A CN201910410007A CN110180410A CN 110180410 A CN110180410 A CN 110180410A CN 201910410007 A CN201910410007 A CN 201910410007A CN 110180410 A CN110180410 A CN 110180410A
Authority
CN
China
Prior art keywords
ultrafiltration membrane
mass parts
blended ultrafiltration
blended
solution
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.)
Pending
Application number
CN201910410007.3A
Other languages
Chinese (zh)
Inventor
迟莉娜
邱静雅
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shenzhen Xinnajie Technology Co Ltd
Original Assignee
Shenzhen Xinnajie Technology Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Shenzhen Xinnajie Technology Co Ltd filed Critical Shenzhen Xinnajie Technology Co Ltd
Priority to CN201910410007.3A priority Critical patent/CN110180410A/en
Publication of CN110180410A publication Critical patent/CN110180410A/en
Pending legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D61/00Processes of separation using semi-permeable membranes, e.g. dialysis, osmosis or ultrafiltration; Apparatus, accessories or auxiliary operations specially adapted therefor
    • B01D61/14Ultrafiltration; Microfiltration
    • B01D61/145Ultrafiltration
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D67/00Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
    • B01D67/0002Organic membrane manufacture
    • B01D67/0009Organic membrane manufacture by phase separation, sol-gel transition, evaporation or solvent quenching
    • B01D67/0013Casting processes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D71/00Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
    • B01D71/06Organic material
    • B01D71/38Polyalkenylalcohols; Polyalkenylesters; Polyalkenylethers; Polyalkenylaldehydes; Polyalkenylketones; Polyalkenylacetals; Polyalkenylketals
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D71/00Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
    • B01D71/06Organic material
    • B01D71/58Other polymers having nitrogen in the main chain, with or without oxygen or carbon only
    • B01D71/62Polycondensates having nitrogen-containing heterocyclic rings in the main chain
    • B01D71/64Polyimides; Polyamide-imides; Polyester-imides; Polyamide acids or similar polyimide precursors
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D71/00Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
    • B01D71/06Organic material
    • B01D71/66Polymers having sulfur in the main chain, with or without nitrogen, oxygen or carbon only
    • B01D71/68Polysulfones; Polyethersulfones

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Water Supply & Treatment (AREA)
  • Dispersion Chemistry (AREA)
  • Manufacturing & Machinery (AREA)
  • Separation Using Semi-Permeable Membranes (AREA)

Abstract

The present invention provides a kind of adjustable blended ultrafiltration membranes in aperture, it is prepared by following steps: the mixture of 65~82 mass parts solvents, 0~10 mass parts polyethylene glycol, 10~20 mass parts polyether sulfones and 0~10 mass parts polymer is added in container, a period of time is stirred with certain mixing speed under solution temperature, dissolve polyether sulfone and polymer, then the standing and defoaming under solution temperature, is made casting solution;On a support by casting solution coating, primary membrane is made;Primary membrane is immersed in coagulating bath, submergence solidification is carried out;Residual solvent is removed, dries later, obtains blended ultrafiltration membrane.Blended ultrafiltration membrane of the invention has high-throughput, high selection permeability and excellent mechanical property, can be applied in the purification and processing of water resource.

Description

A kind of adjustable blended ultrafiltration membrane in aperture
Technical field
The present invention relates to technical field of membrane separation, more particularly, to a kind of adjustable blended ultrafiltration membrane in aperture.
Background technique
The membrane separation technique advanced technology emerging as 21 century, because its with it is easy to operate, without phase-change, without chemistry become The advantages of conventional separation methods such as change, energy conservation, treatment effeciency height do not have, membrane separation technique are separated in gas-liquid and liquid liquid etc. Field is widely used.Wherein ultrafiltration is a kind of important membrane separating process;The average pore size of ultrafiltration membrane is 0.01 micro- Rice~0.1 micron, ultra-filtration process are to apply the power of 0.1-1Mpa or so according to aperture screening mechanism in film side, penetrate water Film is mainly used to filter the solution containing fine particle or bigger molecule.Suspended material, the colloid in water can be effectively removed Grain, microorganism, bacterial virus and some macromolecular dissolved organic matters, are widely used in drinking water treatment, have wide Prospect.
In numerous polymeric film materials, polyether sulfone has good inoxidizability, thermal stability and excellent film forming Property;Polyimides as a kind of aroma type polymer, unique structure make it have pressure-resistant high temperature resistant and chemicals-resistant corrosion Performance has good resistance to toluene, hydrocarbon, pure and mild ketone etc., has been widely used in the preparation of ultrafiltration membrane material.
Life science, bioengineering, pharmaceuticals industry and food industry development, provide more attractive for ultrafiltration membrane Application space, while higher requirements are also raised to ultrafiltration membrane material: (1) it is high-throughput;(2) have accurate adjustable aperture big Small and relatively narrow pore-size distribution.Theoretically, the macroscopic property for being film-made liquid system determines finally at membrane structure and hole Rate, solvent, non-solvent phase counterdiffusion dynamic process determine film pore size and pore-size distribution.
Summary of the invention
The present invention provides a kind of adjustable interpenetrating networks bicontinuous structure blended ultrafiltration membrane in aperture, which is hole Diameter is controllable, structure-controllable, the fluorocarbon polymer microporous barrier with high-throughput, highly selective and excellent mechanical property.
The present invention provides a kind of blended ultrafiltration membranes, wherein the blended ultrafiltration membrane passes through following steps and prepares: by 65~ The mixing of 82 mass parts solvents, 0~10 mass parts polyethylene glycol, 10~20 mass parts polyether sulfones and 0~10 mass parts polymer Object is added in container, is stirred a period of time under solution temperature with certain mixing speed, is made the polyether sulfone and the polymerization Object dissolution, then the standing and defoaming under the solution temperature, is made casting solution;On a support by casting solution coating, system At primary membrane;The primary membrane is immersed in coagulating bath, submergence solidification is carried out;Residual solvent is removed, dries later, obtains institute State blended ultrafiltration membrane.
In above-mentioned blended ultrafiltration membrane, wherein the solvent includes dimethylformamide, dimethyl acetamide, N- methyl One of pyrrolidones, dimethyl sulfoxide, butyl acetate, butyrolactone are a variety of.
In above-mentioned blended ultrafiltration membrane, wherein the polymer includes one in polyamide, polyimides and its derivative Kind is a variety of.
In above-mentioned blended ultrafiltration membrane, wherein in the casting solution, formed by the polyether sulfone and the polymer The mass percentage of copolymer is 16%~30%.
In above-mentioned blended ultrafiltration membrane, wherein in the casting solution, the mass percentage of the solvent is 70%~ 82%.
In above-mentioned blended ultrafiltration membrane, wherein the temperature of the coagulating bath is 25~80 DEG C.
In above-mentioned blended ultrafiltration membrane, wherein the coagulating bath is the mixed solution of ethyl alcohol and water, and the ethyl alcohol is described Mass percentage in mixed solution is 0~60%.
In above-mentioned blended ultrafiltration membrane, wherein the solution temperature be 30 DEG C~65 DEG C, the mixing speed be 100 turns/ Minute~600 revs/min, the time of stirring is 8 hours~24 hours.
The present invention induces the method mutually separated using non-solvent, and it is double can to prepare a series of controllable interpenetrating networks in apertures The section of the blended ultrafiltration membrane of continuous pore structure, the ultrafiltration membrane is uniform interpenetrating networks co-continuous pore structure, and passes through tune Preparation condition is controlled, it is available with different pore size and with the ultrafiltration membrane of uniform interpenetrating networks co-continuous pore structure.This The ultrafiltration membrane of invention has high-throughput, high selection permeability and excellent mechanical property, purification and place applied to water resource In reason, it can be used for retaining the material of different molecular weight.
Detailed description of the invention
Fig. 1 is the cross section structure scanning electron microscope (SEM) photograph of blended ultrafiltration membrane prepared by embodiment 1.
Fig. 2 is the cross section structure scanning electron microscope (SEM) photograph of blended ultrafiltration membrane prepared by embodiment 5.
Fig. 3 is the cross section structure scanning electron microscope (SEM) photograph of blended ultrafiltration membrane prepared by embodiment 10.
Fig. 4 is blended ultrafiltration membrane pore-size distribution histogram prepared by embodiment 1.
Fig. 5 is blended ultrafiltration membrane pore-size distribution histogram prepared by embodiment 5.
Fig. 6 is blended ultrafiltration membrane pore-size distribution histogram prepared by embodiment 10.
Specific embodiment
The following examples can make those skilled in the art that the present invention be more fully understood, but not limit in any way The present invention.
The present invention provides a kind of adjustable interpenetrating networks bicontinuous structure blended ultrafiltration membrane in aperture, preparation method includes Following steps:
(1) by 65~82 mass parts solvents, 0~10 mass parts polyethylene glycol and 10~20 mass parts polyether sulfones and 0~ The mixture of 10 mass parts polymer is added in container, in certain solution temperature, certain mixing speed and certain mixing time It inside dissolves various polymer, then casting solution is made within standing and defoaming 12~24 hours at the same temperature;Solution temperature is 30 DEG C~65 DEG C, mixing speed is 100 revs/min~600 revs/min, and mixing time is 8 hours~24 hours;Wherein, solvent packet Include dimethylformamide, dimethyl acetamide, N-Methyl pyrrolidone, dimethyl sulfoxide, butyl acetate, one in butyrolactone Kind is a variety of, and polymer includes one of polyamide, polyimides and its derivative or a variety of;
(2) primary membrane, evaporation time of the control primary membrane in air is made in casting solution blade coating on a flat support object For 0~2h, wherein flat support object can be made of any suitable materials such as plastics, metals;
(3) primary membrane is immersed in 0~90 DEG C of coagulating bath, carries out the submergence solidification of 24~48h;The coagulating bath It is the mixed solution of ethyl alcohol and pure water, wherein mass percentage of the ethyl alcohol in mixed solution is 0%~60%;
(4) it is dried after removing residual solvent, obtains the adjustable interpenetrating networks bicontinuous structure blended ultrafiltration membrane in aperture.
It is illustrated below with reference to specific embodiment, so that those skilled in the art more fully understand the present invention.Flux And retention test unification is carried out with 8010 ultrafiltration apparatus of Mi Libo Amicon stirring-type, the effective area of measuring device is 4.1cm2, test before water flux that precompressed 30min stablizes membrane flux under 0.15Mpa pressure, after survey it under 0.1Mpa pressure again Water flux.Cutoff performance is evaluated with molecular cut off (MWCO:molecular weight cutoff).Film is to being trapped object When the rejection of matter is greater than 90%, the cutoff performance of film, referred to as the retention molecule of film are just indicated with the molecular weight for being trapped substance Amount.
Embodiment 1
By 76 mass parts butyrolactones, 8 mass parts polyethylene glycol and 12 mass parts polyether sulfones and 4 mass parts polyimides Mixture be added in container, constant solution temperature, constant agitation speed keep various polymer molten in the constant agitation time Solution, is then made casting solution in standing and defoaming 24 hours at the same temperature;Solution temperature is 60 DEG C, and mixing speed is 200 revs/min Clock, mixing time are 12 hours;Primary membrane is made on a flat support object in casting solution blade coating, controls it in the evaporation of air Time is 0min;Being immersed into temperature afterwards is in 60 DEG C of deionized water coagulating bath, is placed in film after film Automatic-falling clean For 24 hours to be dried after the remaining solvent of removing in deionized water.Up to interpenetrating interpenetrating networks bicontinuous structure polyether sulfone/polyimides Blended ultrafiltration membrane.
This blended ultrafiltration membrane water flux at 0.1MPa is 688L/m after tested2H, molecular cut off 100KDa.
Embodiment 2
By 76 mass parts butyrolactones, 8 mass parts polyethylene glycol and 12 mass parts polyether sulfones and 4 mass parts polyimides Mixture be added in container, constant solution temperature, constant agitation speed keep various polymer molten in the constant agitation time Solution, is then made casting solution in standing and defoaming 24 hours at the same temperature;Solution temperature is 60 DEG C, and mixing speed is 200 revs/min Clock, mixing time are 12 hours;Primary membrane is made on a flat support object in casting solution blade coating, controls it in the evaporation of air Time is 0min;Being immersed into temperature afterwards is in 80 DEG C of deionized water coagulating bath, is placed in film after film Automatic-falling clean For 24 hours to be dried after the remaining solvent of removing in deionized water.Up to interpenetrating interpenetrating networks bicontinuous structure polyether sulfone/polyimides Blended ultrafiltration membrane.
This blended ultrafiltration membrane water flux at 0.1MPa is 127L/m after tested2H, molecular cut off 43KDa.
Embodiment 3
By 76 mass parts butyrolactones, 8 mass parts polyethylene glycol and 12 mass parts polyether sulfones and 4 mass parts polyimides Mixture be added in container, in constant solution temperature, constant agitation speed, keep various polymer molten in the constant agitation time Solution, is then made casting solution in standing and defoaming 24 hours at the same temperature;Solution temperature is 60 DEG C, and mixing speed is 200 revs/min Clock, mixing time are 12 hours;Primary membrane is made on a flat support object in casting solution blade coating, controls it in the evaporation of air Time is 0min;It is immersed into the ethanol water coagulating bath that the mass fraction that temperature is 25 DEG C is 15%, is taken off automatically to film afterwards Fall behind and is dried after film to be placed in in clean deionized water the solvent to remove remnants for 24 hours.Up to interpenetrating interpenetrating networks co-continuous Structural polyether sulfone/polyimides blended ultrafiltration membrane.
This blended ultrafiltration membrane water flux at 0.1MPa is 90L/m after tested2H, molecular cut off 22KDa.
Embodiment 4
By 76 mass parts butyrolactones, 8 mass parts polyethylene glycol and 12 mass parts polyether sulfones and 4 mass parts polyimides Mixture be added in container, in constant solution temperature, constant agitation speed, keep various polymer molten in the constant agitation time Solution, is then made casting solution in standing and defoaming 24 hours at the same temperature;Solution temperature is 60 DEG C, and mixing speed is 200 revs/min Clock, mixing time are 12 hours;Primary membrane is made on a flat support object in casting solution blade coating, controls it in the evaporation of air Time is 0min;It is immersed into the ethanol water coagulating bath that the mass fraction that temperature is 25 DEG C is 50%, is taken off automatically to film afterwards Fall behind and is dried after film to be placed in in clean deionized water the solvent to remove remnants for 24 hours.Up to interpenetrating interpenetrating networks co-continuous Structural polyether sulfone/polyimides blended ultrafiltration membrane.
This blended ultrafiltration membrane water flux at 0.1MPa is 65L/m after tested2H, molecular cut off 10KDa.
Embodiment 5
By 74 mass parts butyrolactones, 8 mass parts polyethylene glycol and 14 mass parts polyether sulfones and 4 mass parts polyimides Mixture be added in container, constant solution temperature, constant agitation speed keep various polymer molten in the constant agitation time Solution, is then made casting solution in standing and defoaming 24 hours at the same temperature;The solution temperature is 60 DEG C, mixing speed 200 Rev/min, mixing time is 12 hours;Primary membrane is made on a flat support object in casting solution blade coating, controls it in air Evaporation time be 0min;It is immersed into the deionized water coagulating bath that temperature is 60 DEG C, is placed in film afterwards after film Automatic-falling For 24 hours to be dried after the remaining solvent of removing in clean deionized water.Up to interpenetrating interpenetrating networks bicontinuous structure polyether sulfone/poly- Acid imide blended ultrafiltration membrane.
This blended ultrafiltration membrane water flux at 0.1MPa is 108L/m after tested2H, molecular cut off 57KDa.
Embodiment 6
By 64 mass parts butyrolactones, 10 mass parts dimethylformamides, 8 mass parts polyethylene glycol and 14 mass parts are poly- The mixture of ether sulfone and 4 mass parts polyimides is added in container, in constant solution temperature, constant agitation speed, constant is stirred Mixing dissolves various polymer in the time, then casting solution is made within standing and defoaming 24 hours at the same temperature;Solution temperature is 60 DEG C, mixing speed is 200 revs/min, and mixing time is 12 hours;Casting solution blade coating is made just on a flat support object Filming, controlling it in the evaporation time of air is 0min;It is immersed into the deionized water coagulating bath that temperature is 25 DEG C afterwards, certainly to film It moves and is dried after film to be placed in in clean deionized water the solvent to remove remnants for 24 hours after falling off.It is double up to interpenetrating interpenetrating networks Continuous structure polyether sulfone/polyimides blended ultrafiltration membrane.
This blended ultrafiltration membrane water flux at 0.1MPa is 160L/m after tested2H, molecular cut off 67KDa.
Embodiment 7
By 64 mass parts butyrolactones, 10 mass parts dimethylformamides, 8 mass parts polyethylene glycol and 14 mass parts are poly- The mixture of ether sulfone and 4 mass parts polyimides is added in container, in constant solution temperature, constant agitation speed, constant is stirred Mixing dissolves various polymer in the time, then casting solution is made within standing and defoaming 24 hours at the same temperature;Solution temperature is 60 DEG C, mixing speed is 200 revs/min, and mixing time is 12 hours;Casting solution blade coating is made just on a flat support object Filming, controlling it in the evaporation time of air is 0min;It is immersed into the deionized water coagulating bath that temperature is 40 DEG C afterwards, certainly to film It moves and is dried after film to be placed in in clean deionized water the solvent to remove remnants for 24 hours after falling off.It is double up to interpenetrating interpenetrating networks Continuous structure polyether sulfone/polyimides blended ultrafiltration membrane.
This blended ultrafiltration membrane water flux at 0.1MPa is 108L/m after tested2H, molecular cut off 67KDa.
Embodiment 8
64 mass parts butyrolactones, 10 mass parts dimethylformamides, 8 mass parts polyethylene glycol and 14 mass parts are gathered The mixture of ether sulfone and 4 mass parts polyimides is added in container, in constant solution temperature, constant agitation speed, constant is stirred Mixing dissolves various polymer in the time, then casting solution is made within standing and defoaming 24 hours at the same temperature;The dissolution temperature Degree is 60 DEG C, and mixing speed is 200 revs/min, and mixing time is 12 hours;Casting solution blade coating is made on a flat support object At primary membrane, controlling it in the evaporation time of air is 0min;It is immersed into the second that the mass fraction that temperature is 25 DEG C is 15% afterwards In alcohol solution coagulating bath, film is placed in after film Automatic-falling in clean deionized water for 24 hours to remove remaining solvent after It dries.Up to interpenetrating interpenetrating networks bicontinuous structure polyether sulfone/polyimides blended ultrafiltration membrane.
This blended ultrafiltration membrane water flux at 0.1MPa is 54L/m after tested2H, molecular cut off 4KDa.
Embodiment 9
It will be by 64 mass parts butyrolactones, 10 mass parts dimethylformamides, 8 mass parts polyethylene glycol and 14 mass parts The mixture of polyether sulfone and 4 mass parts polyimides is added in container, in constant solution temperature, constant agitation speed, constant It dissolves various polymer in mixing time, then casting solution is made within standing and defoaming 24 hours at the same temperature;Solution temperature It is 60 DEG C, mixing speed is 200 revs/min, and mixing time is 12 hours;Casting solution blade coating is made on a flat support object Primary membrane, controlling it in the evaporation time of air is 0min;It is immersed into the ethyl alcohol that the mass fraction that temperature is 25 DEG C is 50% afterwards In aqueous coagulation bath, film is placed in clean deionized water for 24 hours to dry in the air after the remaining solvent of removing after film Automatic-falling It is dry.Up to interpenetrating interpenetrating networks bicontinuous structure polyether sulfone/polyimides blended ultrafiltration membrane.
This blended ultrafiltration membrane water flux at 0.1MPa is 40L/m after tested2H, molecular cut off 2KDa.
Embodiment 10
By 52 mass parts butyrolactones, 20 mass parts dimethylformamides, 8 mass parts polyethylene glycol and 16 mass parts are poly- The mixture of ether sulfone and 4 mass parts polyimides is added in container, in constant solution temperature, constant agitation speed, constant is stirred Mixing dissolves various polymer in the time, then casting solution is made within standing and defoaming 24 hours at the same temperature;Solution temperature is 60 DEG C, mixing speed is 200 revs/min, and mixing time is 12 hours;Casting solution blade coating is made just on a flat support object Filming, controlling it in the evaporation time of air is 0min;It is immersed into the deionized water coagulating bath that temperature is 60 DEG C afterwards, certainly to film It moves and is dried after film to be placed in in clean deionized water the solvent to remove remnants for 24 hours after falling off.It is double up to interpenetrating interpenetrating networks Continuous structure polyether sulfone/polyimides blended ultrafiltration membrane.
This blended ultrafiltration membrane water flux at 0.1MPa is 160L/m after tested2H, molecular cut off 43KDa.
Embodiment 11
By 82 mass parts dimethylformamides, 2 mass parts polyethylene glycol and 10 mass parts polyether sulfones and 6 mass parts polyamides The mixture of imines is added in container, in constant solution temperature, constant agitation speed, makes various polymerizations in the constant agitation time Object dissolution, is then made casting solution in standing and defoaming 24 hours at the same temperature;The solution temperature is 60 DEG C, and mixing speed is 200 revs/min, mixing time is 12 hours;Primary membrane is made on a flat support object in casting solution blade coating, controls it in sky The evaporation time of gas is 0min;It is immersed into the 15% ethanol water coagulating bath that temperature is 25 DEG C afterwards, after film Automatic-falling It is dried after film to be placed in in clean deionized water the solvent to remove remnants for 24 hours.Up to interpenetrating interpenetrating networks bicontinuous structure Polyether sulfone/polyimides blended ultrafiltration membrane.
This blended ultrafiltration membrane water flux at 0.1MPa is 700L/m after tested2H, molecular cut off 120KDa.
Embodiment 12
65 mass parts dimethyl acetamides, 10 mass parts polyethylene glycol and 15 mass parts polyether sulfones and 10 mass parts are gathered Imido mixture is added in container, in constant solution temperature, constant agitation speed, makes various gather in the constant agitation time Object dissolution is closed, then casting solution is made within standing and defoaming 24 hours at the same temperature;The solution temperature is 60 DEG C, mixing speed It is 200 revs/min, mixing time is 12 hours;On a flat support object primary membrane is made in casting solution blade coating, control its The evaporation time of air is 0min;It is immersed into the 50% ethanol water coagulating bath that temperature is 25 DEG C afterwards, to film Automatic-falling It is dried after film to be placed in in clean deionized water the solvent to remove remnants for 24 hours afterwards.Up to interpenetrating interpenetrating networks co-continuous knot Structure polyether sulfone/polyimides blended ultrafiltration membrane.
This blended ultrafiltration membrane water flux at 0.1MPa is 90L/m after tested2H, molecular cut off 67KDa.
Embodiment 13
The mixture of 72 mass parts N-Methyl pyrrolidones, 20 mass parts polyether sulfones and 8 mass parts polyimides is added Into container, dissolve polymer in the time in constant solution temperature, constant agitation speed, constant agitation, then in Xiang Tongwen It spends lower standing and defoaming and casting solution is made in 24 hours;Solution temperature is 60 DEG C, and mixing speed is 200 revs/min, mixing time 12 Hour;Primary membrane is made on a flat support object in casting solution blade coating, controlling it in the evaporation time of air is 0min;After soak Being less than temperature is in 60 DEG C of deionized water coagulating bath, film is placed in after film Automatic-falling in clean deionized water for 24 hours with It is dried after removing remaining solvent.Up to interpenetrating interpenetrating networks bicontinuous structure polyether sulfone/polyimides blended ultrafiltration membrane.
This blended ultrafiltration membrane water flux at 0.1MPa is 68L/m after tested2H, molecular cut off 43KDa.
Embodiment 14
72 mass parts dimethyl sulfoxides, 5 mass parts polyethylene glycol and 16 mass parts polyether sulfones and 4 mass parts polyamides are sub- The mixture of amine is added in container, in constant solution temperature, constant agitation speed, keeps polymer molten in the constant agitation time Solution, is then made casting solution in standing and defoaming 24 hours at the same temperature;Solution temperature is 60 DEG C, and mixing speed is 200 revs/min Clock, mixing time are 12 hours;Primary membrane is made on a flat support object in casting solution blade coating, controls it in the evaporation of air Time is 120min;It is immersed into the deionized water coagulating bath that temperature is 60 DEG C, is placed in film completely afterwards after film Automatic-falling Deionized water in for 24 hours to dry after removing remaining solvent.It is sub- up to interpenetrating interpenetrating networks bicontinuous structure polyether sulfone/polyamides Amine blended ultrafiltration membrane.
This blended ultrafiltration membrane water flux at 0.1MPa is 150L/m after tested2H, molecular cut off 67KDa.
Embodiment 15
By 50 mass parts butyrolactones, 20 mass parts N-Methyl pyrrolidones, 10 mass parts polyethylene glycol and 16 mass The mixture of part polyether sulfone and 4 mass parts polyamide is added in container, in constant solution temperature, constant agitation speed, constant Polymer is dissolved in mixing time, then casting solution is made within standing and defoaming 24 hours at the same temperature;Solution temperature is 60 DEG C, mixing speed is 200 revs/min, and mixing time is 12 hours;Casting solution blade coating is made on a flat support object nascent Film, controlling it in the evaporation time of air is 0min;It is immersed into the deionized water coagulating bath that temperature is 60 DEG C afterwards, it is automatic to film Film is placed in clean deionized water for 24 hours to dry after the remaining solvent of removing after falling off.Up to interpenetrating interpenetrating networks doubly-linked Continuous structural polyether sulfone/polyamide blended ultrafiltration membrane.
This blended ultrafiltration membrane water flux at 0.1MPa is 135L/m after tested2H, molecular cut off 67KDa.
It will be understood by those skilled in the art that above embodiments are only exemplary embodiments, without departing substantially from spirit of the invention In the case where range, a variety of variations can be carried out, replaced and changed.

Claims (8)

1. a kind of blended ultrafiltration membrane, wherein the blended ultrafiltration membrane is prepared by following steps:
65~82 mass parts solvents, 0~10 mass parts polyethylene glycol, 10~20 mass parts polyether sulfones and 0~10 mass parts are gathered The mixture for closing object is added in container, is stirred a period of time under solution temperature with certain mixing speed, is made the polyether sulfone It is dissolved with the polymer, then the standing and defoaming under the solution temperature, is made casting solution;
On a support by casting solution coating, primary membrane is made;
The primary membrane is immersed in coagulating bath, submergence solidification is carried out;
Residual solvent is removed, dries later, obtains the blended ultrafiltration membrane.
2. blended ultrafiltration membrane according to claim 1, wherein the solvent includes dimethylformamide, dimethylacetamide One of amine, N-Methyl pyrrolidone, dimethyl sulfoxide, butyl acetate, butyrolactone are a variety of.
3. blended ultrafiltration membrane according to claim 1, wherein the polymer includes polyamide, polyimides and its spreads out One of biology is a variety of.
4. blended ultrafiltration membrane according to claim 1, wherein in the casting solution, by the polyether sulfone and described poly- The mass percentage for closing the copolymer that object is formed is 16%~30%.
5. blended ultrafiltration membrane according to claim 1, wherein in the casting solution, the quality percentage of the solvent contains Amount is 70%~82%.
6. blended ultrafiltration membrane according to claim 1, wherein the temperature of the coagulating bath is 25~80 DEG C.
7. blended ultrafiltration membrane according to claim 1, wherein the coagulating bath is the mixed solution of ethyl alcohol and water, described Mass percentage of the ethyl alcohol in the mixed solution is 0~60%.
8. blended ultrafiltration membrane according to claim 1, wherein the solution temperature is 30 DEG C~65 DEG C, the stirring speed Degree is 100 revs/min~600 revs/min, and the time of stirring is 8 hours~24 hours.
CN201910410007.3A 2019-05-16 2019-05-16 A kind of adjustable blended ultrafiltration membrane in aperture Pending CN110180410A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910410007.3A CN110180410A (en) 2019-05-16 2019-05-16 A kind of adjustable blended ultrafiltration membrane in aperture

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910410007.3A CN110180410A (en) 2019-05-16 2019-05-16 A kind of adjustable blended ultrafiltration membrane in aperture

Publications (1)

Publication Number Publication Date
CN110180410A true CN110180410A (en) 2019-08-30

Family

ID=67716434

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910410007.3A Pending CN110180410A (en) 2019-05-16 2019-05-16 A kind of adjustable blended ultrafiltration membrane in aperture

Country Status (1)

Country Link
CN (1) CN110180410A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114405276A (en) * 2021-12-27 2022-04-29 浙江易膜新材料科技有限公司 Preparation method of high-temperature-resistant separation membrane material

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103846016A (en) * 2014-03-10 2014-06-11 南京工业大学 Preparation method of polyether sulfone polyimide blended ultrafiltration membrane
CN105327622A (en) * 2014-06-19 2016-02-17 中国石油化工股份有限公司 Preparation method of flat hybridization ultrafiltration membrane used for water treatment
CN106731866A (en) * 2016-12-02 2017-05-31 宁波沃浦膜科技有限公司 A kind of preparation method for weaving tube enhancement type hollow fiber ultrafiltration membrane

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103846016A (en) * 2014-03-10 2014-06-11 南京工业大学 Preparation method of polyether sulfone polyimide blended ultrafiltration membrane
CN105327622A (en) * 2014-06-19 2016-02-17 中国石油化工股份有限公司 Preparation method of flat hybridization ultrafiltration membrane used for water treatment
CN106731866A (en) * 2016-12-02 2017-05-31 宁波沃浦膜科技有限公司 A kind of preparation method for weaving tube enhancement type hollow fiber ultrafiltration membrane

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
王多仁: "《绿色净水处理剂》", 30 November 2006 *
王湛: "《膜分离技术基础》", 30 April 2000 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114405276A (en) * 2021-12-27 2022-04-29 浙江易膜新材料科技有限公司 Preparation method of high-temperature-resistant separation membrane material

Similar Documents

Publication Publication Date Title
Kong et al. Preparation of PVDF hollow‐fiber membranes via immersion precipitation
Bottino et al. High performance ultrafiltration membranes cast from LiCl doped solutions
Mohammadi et al. Effect of production conditions on morphology and permeability of asymmetric cellulose acetate membranes
CN100411722C (en) Porous polyvinylidene blending porous membrane and process for producing same
Shin et al. Preparation and characterization of polyethersulfone microfiltration membranes by a 2-methoxyethanol additive
EP1166859A3 (en) Porous hollow fiber membranes and method of making the same
CN102160969B (en) Method for preparing fluorocarbon polymer microporous film with interpenetrating network bicontinuous pore structure
CN111167316B (en) Normal-temperature selective swelling and perforating method for preparing separation membrane
CN104415667A (en) Method of modifying polyolefin ultrafiltration membrane through polyaniline in-situ polymerization method
CN108499361B (en) Preparation method of nano-porous polymer film with adjustable pore size
CN103406030A (en) Preparation method of gas-phase crosslinking modified polyetherimide nanofiltration membrane
CN110180410A (en) A kind of adjustable blended ultrafiltration membrane in aperture
CN110180409A (en) A kind of preparation method of the adjustable blended ultrafiltration membrane in aperture
CN112044291A (en) Compact separation membrane
CN108014658B (en) Preparation method for preparing porous gelatin film from Graphene Oxide (GO) stable Pickering emulsion
Tang et al. A novel positively charged asymmetry membranes from poly (2, 6-dimethyl-1, 4-phenylene oxide) by benzyl bromination and in situ amination: membrane preparation and characterization
CN110975649A (en) Modified polyvinylidene fluoride ultrafiltration membrane and preparation method thereof
CN114917764A (en) Method for preparing high-selectivity high-flux PES ultrafiltration membrane by utilizing monomer self-crosslinking
CN103285743B (en) Hydrophilization modification method for polyvinyl chloride alloy ultrafiltration membrane
CN109433027A (en) A kind of hydrophilic antipollution ultrafiltration membrane and preparation method thereof
CN110124539A (en) Microwave-enhanced selective swelling and perforating method for separation membrane
CN106621837B (en) A kind of hydrophilic modifying network cross-linked object perforated membrane and preparation method thereof
Haraya et al. Asymmetric capillary membrane of a carbon molecular sieve
CN104801209A (en) Ultralow-pressure nanofiltration membrane prepared from imidazole sulfonate grafted polyether sulfone
CN109621745B (en) Method for preparing microfiltration membrane by dry-wet phase conversion

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20190830