CN108752824A - A kind of preparation method of dialysis capillary fibers - Google Patents

A kind of preparation method of dialysis capillary fibers Download PDF

Info

Publication number
CN108752824A
CN108752824A CN201810625615.1A CN201810625615A CN108752824A CN 108752824 A CN108752824 A CN 108752824A CN 201810625615 A CN201810625615 A CN 201810625615A CN 108752824 A CN108752824 A CN 108752824A
Authority
CN
China
Prior art keywords
parts
preparation
dialysis
capillary
capillary fibers
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
CN201810625615.1A
Other languages
Chinese (zh)
Inventor
王美霞
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.)
Beijing Dianyu Technology Co Ltd
Original Assignee
Beijing Dianyu 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 Beijing Dianyu Technology Co Ltd filed Critical Beijing Dianyu Technology Co Ltd
Priority to CN201810625615.1A priority Critical patent/CN108752824A/en
Publication of CN108752824A publication Critical patent/CN108752824A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/42Nitriles
    • C08F220/44Acrylonitrile
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L33/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • C08L33/18Homopolymers or copolymers of nitriles
    • C08L33/20Homopolymers or copolymers of acrylonitrile
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2203/00Applications
    • C08L2203/12Applications used for fibers

Abstract

The invention belongs to therapeutic technical fields, and in particular to a kind of preparation method of dialysis capillary fibers.A kind of preparation method of dialysis capillary fibers is:By mass fraction be 100-120 parts of acrylic fiber ternary copolymer fibre, 100-150 parts of solvent, 2-3 parts of auxiliary agent, 0.1-0.2 parts of antioxidant, 1-2 parts of reinforcing agent mix, and solution progress dry method extrusion molding can be obtained by the capillary fibers of required diameter after mixing;A kind of preparation method of dialysis capillary fibers proposed by the present invention;Capillary fibers are prepared by way of continuously squeezing out, and are used as main basis material by adding acrylic fiber ternary copolymer fibre so that the capillary fibers have intensity high, and the excellent performance such as corrosion-resistant can put into routine use.

Description

A kind of preparation method of dialysis capillary fibers
Technical field
The invention belongs to field of medical technology, and in particular to a kind of preparation method of dialysis capillary fibers.
Background technology
Dialysis is to be diffused into the principle of water (or buffer solution) through semi-permeable membrane by small molecule, and small molecule is divided greatly with biology A kind of separated separating and purifying technology of son.Dialysis therapy is to make the ingredient (solute or moisture) in body fluid that body be discharged by semi-permeable membrane Outer therapy generally can be divided into two kinds of haemodialysis and peritoneal dialysis.
101883624 A of Chinese patent application CN disclose the preparation of doughnut, are related to composite hollow fibre capillary Film, it is especially useful in using dialyzate value and its production method and its purposes especially in blood and peritoneal dialysis.
105693935 A of Chinese patent application CN disclose a kind of hydroxyethyl cellulose modified object of bisexual ion purification and its Preparation method and purposes, the invention is using ammonium ceric nitrate and disodium ethylene diamine tetraacetate as redox initiation system, using 3- (2- Methylacryoyloxyethyl dimethylamino) propane sulfonic acid salt zwitterionic monomer to hydroxyethyl cellulose carry out grafting, copolymerization and modification, The hydroxyethyl cellulose modified object of bisexual ion purification is made.Compared with unmodified hydroxyethyl cellulose, bisexual ion purification ethoxy is fine The plain modifier of dimension, which is more easy to be attached to capillary tube inner wall surface, forms stable coating, and then reduces protein in capillary tube inner wall table The absorption in face, the efficiency for improving capillary electrophoresis separation protein;Moreover, modifier coating is formed by also with wider The pH scope of applications, variety classes, different isoelectric point protein macromolecule can more effectively be detached.
But it is still grown a lot space with capillary fibers field in dialysis, because the invention proposes a kind of dialysis use The preparation method of capillary fibers.
Invention content
In order to achieve the purpose that in background technology, a kind of preparation method of dialysis capillary fibers proposed by the present invention; The present invention prepares capillary fibers by way of continuously squeezing out, and is used as by addition acrylic fiber ternary copolymer fibre main Basis material so that the capillary fibers have intensity high, and the excellent performance such as corrosion-resistant can put into routine use.
What the present invention realized by the following technical solutions
A kind of a kind of preparation method of dialysis capillary fibers, which is characterized in that dialysis capillary fibers Preparation method be:It is 100-120 parts of acrylic fiber ternary copolymer fibre, 100-150 parts of solvent, 2-3 by mass fraction The auxiliary agent, 0.1-0.2 parts of antioxidant, 1-2 parts of reinforcing agent of part are mixed, and after mixing squeeze solution progress dry method Go out the capillary fibers that molding can be obtained by required diameter.
Further, the preparation method is, in a kettle, the acrylic fiber ternary for being 100-120 parts by mass fraction Copolymer fibre is dissolved in 100-150 parts of solvent, carries out high-speed stirred after 1-2 hours, respectively by 2-3 parts of auxiliary agent, 0.1-0.2 parts of antioxidant, 1-2 parts of reinforcing agent are added in reaction kettle, and reaction obtains gelatinous solid after 1-2 hours, Then the substance is added in extruding groove, is squeezed out, mold is changed into the mold of extruding pipe before extrusion, then by dry section The temperature in domain is controlled at 120-150 DEG C, and then length starts to squeeze out in 1-2m, in dry slot back and forth by the filament of extrusion It is 2-3 times dry, the speed of dragger is controlled, the size of capillary inside diameter can be effectively controlled, passes through winding The hollow pipe of function admirable is obtained, then hollow pipe is cut as needed, so that it may to obtain different length specification Capillary, while can also obtain the capillary of different pore size size by controlling hauling speed.
Further, the acrylic fiber ternary copolymer fibre be by mass fraction be 100-120 parts acrylonitrile, 12-20 parts of styrene, 30-35 parts of butyl methacrylate, 100-200 parts of solvent is mixed, and after mixing will It is according to 1:4 ratio is divided into two parts, wherein few part is added in reaction kettle, more parts is added in constant pressure buret; Then it is added in another buret, the solvent of 1-2 parts of benzoyl peroxide and 10-20 part;By two when starting to react A constant pressure buret is opened, and is controlled its drop speed, is made the substance in two burets in 2-3 hours while dripping off, reacting The speed control of blender is in 200-300rpm in journey, it is to be titrated completely after, increase 5-10 DEG C, after isothermal reaction 1-2 hours, stop It only heats, takes out after naturally cooling to room temperature, be then dried, remove solvent, it is exactly acrylic fiber ternary polymerization to obtain substance Fibres.
Further, the solvent is, according to mass ratio is 1-2 by dichloromethane, chloroform, petroleum ether, hexamethylene:3-5: 5-10:The mixed liquor that the ratio of 4-8 is mixed to get.
Further, the auxiliary agent is, by 2-8 parts of dodecyl sodium sulfonate lithium, 1-2 parts of zinc laurate, 2-3 parts Stearic acid, 10-20 parts of solvent carries out mixture prepared substance.
Further, the antioxidant is, by 1-2 parts of P-TOLUENE SULFO ACID 99's sodium, the Pyrogentisinic Acid of 0.2-0.5,1-2 parts Salicylic acid, 10-20 parts of solvent carries out mixture prepared substance.
Further, the reinforcing agent is 10-20 parts of poly- biphenyl, 6-10 parts of polyurethane, 4-8 parts of melamine The substance that amine is prepared after being mixed.
Further, the reaction condition is that temperature is controlled at 70-80 DEG C.
Beneficial to benefit
1, the present invention prepared by way of continuously squeezing out capillary fibers its to prepare speed fast, it is efficient, and pass through this Capillary dimensions prepared by method is controllable, product mechanics uniform properties;
2, by the present invention in that using acrylic fiber ternary copolymer fibre as main basis material, there is intensity height, it is resistance to The excellent performances such as corrosion.
Specific implementation mode
In order to keep the purpose of the present invention, technical solution and advantageous effect clearer, below in conjunction with experimental data, to this The preferred embodiment of invention is described in detail, to facilitate the technical staff to understand.
Embodiment 1
A kind of preparation method of dialysis capillary fibers includes the following steps:
(1) mass fraction is 100-120 parts of acrylonitrile, 12-20 parts of benzene second at 75 DEG C by control temperature of reaction kettle Alkene, 30-35 parts of butyl methacrylate, 200 parts of solvent are mixed, after mixing by it according to 1:4 ratio point At two parts, wherein few part is added in reaction kettle, more parts is added in constant pressure buret;Then in another titration It is added in pipe, 1.5 parts of benzoyl peroxide and 12 parts of solvent;Start to open two constant pressure burets when reaction, control It drips speed, makes the substance in two burets in 2 hours while dripping off, the speed control of blender exists during the reaction 250rpm, it is to be titrated completely after, increase 5 DEG C, after isothermal reaction 2 hours, stop heating, taken out after naturally cooling to room temperature, so After be dried, remove solvent, it is exactly acrylic fiber ternary copolymer fibre to obtain substance;
(2) in a kettle, it is that 120 parts of acrylic fiber ternary copolymer fibre is dissolved in 100 parts molten by mass fraction In agent, high-speed stirred is carried out after 2 hours, and reaction is added in 2 parts of auxiliary agent, 0.1 part of antioxidant, 1 part of reinforcing agent respectively In kettle, reaction obtains gelatinous solid after 2 hours, and then the substance is added in extruding groove, is squeezed out, and before extrusion will Mold changes the mold of extruding pipe into, then controls the temperature of arid region at 125 DEG C, then length starts to squeeze out in 1m, The filament of extrusion is dried 3 times back and forth in dry slot, controls the speed of dragger, can effectively be controlled straight inside capillary The size of diameter can be obtained by the hollow pipe of function admirable by winding, then be cut as needed to hollow pipe, just The capillary of different length specification can be obtained, while the capillary of different pore size size can also be obtained by controlling hauling speed Pipe.
Embodiment 2
A kind of preparation method of dialysis capillary fibers includes the following steps:
(1) control temperature of reaction kettle is at 70 DEG C, by mass fraction be 110 parts of acrylonitrile, 16 parts of styrene, 33 parts Butyl methacrylate, 120 parts of solvent are mixed, after mixing by it according to 1:4 ratio is divided into two parts, In few part be added in reaction kettle, more parts is added in constant pressure buret;Then it is added in another buret, 1 The benzoyl peroxide and 10 parts of solvent of part;Start to open two constant pressure burets when reaction, controls its drop speed, make two Substance in buret drips off simultaneously in 2 hours, and the speed control of blender is to be titrated complete in 230rpm during the reaction Quan Hou increases 5 DEG C, after isothermal reaction 2 hours, stops heating, take out after naturally cooling to room temperature, be then dried, removes Solvent, it is exactly acrylic fiber ternary copolymer fibre to obtain substance;
(2) in a kettle, it is that 110 parts of acrylic fiber ternary copolymer fibre is dissolved in 115 parts molten by mass fraction In agent, high-speed stirred is carried out after 1 hour, and reaction is added in 3 parts of auxiliary agent, 0.1 part of antioxidant, 2 parts of reinforcing agent respectively In kettle, reaction obtains gelatinous solid after 2 hours, and then the substance is added in extruding groove, is squeezed out, and before extrusion will Mold changes the mold of extruding pipe into, then controls the temperature of arid region at 125 DEG C, then length starts to squeeze out in 2m, The filament of extrusion is dried 3 times back and forth in dry slot, controls the speed of dragger, can effectively be controlled straight inside capillary The size of diameter can be obtained by the hollow pipe of function admirable by winding, then be cut as needed to hollow pipe, just The capillary of different length specification can be obtained, while the capillary of different pore size size can also be obtained by controlling hauling speed Pipe.
Embodiment 3
A kind of preparation method of dialysis capillary fibers includes the following steps:
(1) control temperature of reaction kettle is at 72 DEG C, by mass fraction be 120 parts of acrylonitrile, 12 parts of styrene, 35 parts Butyl methacrylate, 160 parts of solvent are mixed, after mixing by it according to 1:4 ratio is divided into two parts, In few part be added in reaction kettle, more parts is added in constant pressure buret;Then it is added in another buret, 1 The benzoyl peroxide and 10 parts of solvent of part;Start to open two constant pressure burets when reaction, controls its drop speed, make two Substance in buret drips off simultaneously in 3 hours, and the speed control of blender is to be titrated complete in 300rpm during the reaction Quan Hou increases 6 DEG C, after isothermal reaction 2 hours, stops heating, take out after naturally cooling to room temperature, be then dried, removes Solvent, it is exactly acrylic fiber ternary copolymer fibre to obtain substance;
(2) in a kettle, it is that 120 parts of acrylic fiber ternary copolymer fibre is dissolved in 150 parts molten by mass fraction In agent, high-speed stirred is carried out after 2 hours, and reaction is added in 3 parts of auxiliary agent, 0.2 part of antioxidant, 2 parts of reinforcing agent respectively In kettle, reaction obtains gelatinous solid after 2 hours, and then the substance is added in extruding groove, is squeezed out, and before extrusion will Mold changes the mold of extruding pipe into, then controls the temperature of arid region at 125 DEG C, then length starts to squeeze out in 2m, The filament of extrusion is dried 3 times back and forth in dry slot, controls the speed of dragger, can effectively be controlled straight inside capillary The size of diameter can be obtained by the hollow pipe of function admirable by winding, then be cut as needed to hollow pipe, just The capillary of different length specification can be obtained, while the capillary of different pore size size can also be obtained by controlling hauling speed Pipe.
Embodiment 4
A kind of preparation method of dialysis capillary fibers includes the following steps:
(1) control temperature of reaction kettle is at 78 DEG C, by mass fraction be 100 parts of acrylonitrile, 18 parts of styrene, 35 parts Butyl methacrylate, 150 parts of solvent are mixed, after mixing by it according to 1:4 ratio is divided into two parts, In few part be added in reaction kettle, more parts is added in constant pressure buret;Then it is added in another buret, 1 The benzoyl peroxide and 10 parts of solvent of part;Start to open two constant pressure burets when reaction, controls its drop speed, make two Substance in buret drips off simultaneously in 2 hours, and the speed control of blender is to be titrated complete in 200rpm during the reaction Quan Hou increases 5 DEG C, after isothermal reaction 1 hour, stops heating, take out after naturally cooling to room temperature, be then dried, removes Solvent, it is exactly acrylic fiber ternary copolymer fibre to obtain substance;
(2) in a kettle, it is that 110 parts of acrylic fiber ternary copolymer fibre is dissolved in 100 parts molten by mass fraction In agent, high-speed stirred is carried out after 1 hour, and reaction is added in 2 parts of auxiliary agent, 0.2 part of antioxidant, 2 parts of reinforcing agent respectively In kettle, reaction obtains gelatinous solid after 2 hours, and then the substance is added in extruding groove, is squeezed out, and before extrusion will Mold changes the mold of extruding pipe into, then controls the temperature of arid region at 130 DEG C, then length starts to squeeze out in 2m, The filament of extrusion is dried 3 times back and forth in dry slot, controls the speed of dragger, can effectively be controlled straight inside capillary The size of diameter can be obtained by the hollow pipe of function admirable by winding, then be cut as needed to hollow pipe, just The capillary of different length specification can be obtained, while the capillary of different pore size size can also be obtained by controlling hauling speed Pipe.
Experimental analysis:
1, capillary Mechanics Performance Testing
The capillary that 1-4 of the embodiment of the present invention capillaries prepared and market are bought, carries out mechanics properties testing, passes through Test, result are as follows:
It may be seen that its mechanical property relative market of the capillary of this method preparation is sold it can be seen from table above The capillary sold is more excellent, and shock strength and tensile strength are superior to commercially available capillary.
2, cost compares
1-4 costs of the embodiment of the present invention are respectively 28 Yuan/㎏, 28.5 Yuan/㎏, 28.6 Yuan/㎏, 29 Yuan/㎏, and commercially available The capillary sold is 42-46 Yuan/㎏, and therefore, product price of the invention is cheap, can be used for large-scale mass production.
3, corrosion resistance is tested
The capillary that 1-4 of the embodiment of the present invention capillaries prepared and market are bought, carries out corrosion-resistant test, tests Method be capillary is respectively placed in strong acid, strong base solution and strong solvent carry out impregnate 1-2 days after, whether observe its surface It changes, by test, result is as follows:
It may be seen that its corrosion resistance relative market of the capillary of this method preparation it can be seen from table above The capillary sold is higher, can be used for medical use.
Finally illustrate, preferred embodiment above is only used to illustrate the technical scheme of the present invention and unrestricted, although logical It crosses above preferred embodiment the present invention is described in detail, however, those skilled in the art should understand that, can be Various changes are made to it in form and in details, defined by claims of the present invention.

Claims (8)

1. a kind of preparation method of dialysis capillary fibers, which is characterized in that a kind of dialysis capillary fibers Preparation method is:By mass fraction be 100-120 parts of acrylic fiber ternary copolymer fibre, 100-150 parts of solvent, 2-3 parts Auxiliary agent, 0.1-0.2 parts of antioxidant, 1-2 parts of reinforcing agent mixed, solution is subjected to dry method extrusion after mixing Molding can be obtained by the capillary fibers of required diameter.
2. a kind of preparation method of dialysis capillary fibers according to claim 1, which is characterized in that the preparation Method is in a kettle, the acrylic fiber ternary copolymer fibre that mass fraction is 100-120 parts to be dissolved in 100-150 parts Solvent in, carry out high-speed stirred after 1-2 hours, respectively by 2-3 parts of auxiliary agent, 0.1-0.2 parts of antioxidant, 1-2 parts Reinforcing agent is added in reaction kettle, and reaction obtains gelatinous solid after 1-2 hours, and then the substance is added in extruding groove, into Row squeezes out, and mold is changed into the mold of extruding pipe before extrusion, then controls the temperature of arid region at 120-150 DEG C, Then length starts to squeeze out in 1-2m, the filament of extrusion is dried 2-3 times back and forth in dry slot, controls the speed of dragger, The size that capillary inside diameter can effectively be controlled can be obtained by the hollow pipe of function admirable by winding, then Hollow pipe is cut as needed, so that it may to obtain the capillary of different length specification, while by controlling hauling speed It can also obtain the capillary of different pore size size.
3. a kind of preparation method of dialysis capillary fibers according to claim 1, which is characterized in that the acrylic fibers Based terpolymers fiber be by mass fraction be 100-120 parts of acrylonitrile, 12-20 parts of styrene, 30-35 parts Butyl methacrylate, 100-200 parts of solvent is mixed, after mixing by it according to 1:4 ratio is divided into two parts, Wherein few part is added in reaction kettle, and more parts is added in constant pressure buret;Then it is added in another buret, The solvent of 1-2 parts of benzoyl peroxide and 10-20 part;Start to open two constant pressure burets when reaction, control its drop speed, Make the substance in two burets in 2-3 hours while dripping off, the speed control of blender is in 200- during the reaction 300rpm, it is to be titrated completely after, increase 5-10 DEG C, after isothermal reaction 1-2 hour, stop heating, be taken after naturally cooling to room temperature Go out, be then dried, removes solvent, it is exactly acrylic fiber ternary copolymer fibre to obtain substance.
4. a kind of preparation method of dialysis capillary fibers according to claim 1, which is characterized in that the solvent For, by dichloromethane, chloroform, petroleum ether, hexamethylene according to mass ratio be 1-2:3-5:5-10:The ratio of 4-8 mix The mixed liquor arrived.
5. a kind of preparation method of dialysis capillary fibers according to claim 1, which is characterized in that the auxiliary agent For 2-8 parts of dodecyl sodium sulfonate lithium, 1-2 parts of zinc laurate, 2-3 parts of stearic acid, 10-20 parts of solvent are mixed Close the substance being prepared.
6. a kind of preparation method of dialysis capillary fibers according to claim 1, which is characterized in that the oxygen Agent is to mix 1-2 parts of P-TOLUENE SULFO ACID 99's sodium, the Pyrogentisinic Acid of 0.2-0.5,1-2 parts of salicylic acid, 10-20 parts of solvent Close the substance being prepared.
7. a kind of preparation method of dialysis capillary fibers according to claim 1, which is characterized in that the enhancing Agent is, the object that 10-20 parts of poly- biphenyl, 6-10 parts of polyurethane, 4-8 parts of melamine is prepared after being mixed Matter.
8. a kind of preparation method of dialysis capillary fibers according to claim 3, which is characterized in that the reaction Condition is that temperature is controlled at 70-80 DEG C.
CN201810625615.1A 2018-06-18 2018-06-18 A kind of preparation method of dialysis capillary fibers Pending CN108752824A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810625615.1A CN108752824A (en) 2018-06-18 2018-06-18 A kind of preparation method of dialysis capillary fibers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810625615.1A CN108752824A (en) 2018-06-18 2018-06-18 A kind of preparation method of dialysis capillary fibers

Publications (1)

Publication Number Publication Date
CN108752824A true CN108752824A (en) 2018-11-06

Family

ID=63978408

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810625615.1A Pending CN108752824A (en) 2018-06-18 2018-06-18 A kind of preparation method of dialysis capillary fibers

Country Status (1)

Country Link
CN (1) CN108752824A (en)

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5236592A (en) * 1990-06-25 1993-08-17 Hospal Industrie Haemocompatible composite material and method of using thereof
CN1958136A (en) * 2006-10-17 2007-05-09 浙江大学 Antibacterial hollow-fiber membrane, preparation method and application
CN101596417A (en) * 2009-06-19 2009-12-09 东华大学 Be used for the preparation of the blend polyvinylidene fluoride hollow-fibre membrane of blood purification
CN101626821A (en) * 2007-04-23 2010-01-13 弗雷泽纽斯医疗保健德国有限公司 Hollow fiber capillary membrane and method for the production thereof
US20140326669A1 (en) * 2011-12-15 2014-11-06 Gambro Lundia Ab Doped membranes

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5236592A (en) * 1990-06-25 1993-08-17 Hospal Industrie Haemocompatible composite material and method of using thereof
CN1958136A (en) * 2006-10-17 2007-05-09 浙江大学 Antibacterial hollow-fiber membrane, preparation method and application
CN101626821A (en) * 2007-04-23 2010-01-13 弗雷泽纽斯医疗保健德国有限公司 Hollow fiber capillary membrane and method for the production thereof
CN101596417A (en) * 2009-06-19 2009-12-09 东华大学 Be used for the preparation of the blend polyvinylidene fluoride hollow-fibre membrane of blood purification
US20140326669A1 (en) * 2011-12-15 2014-11-06 Gambro Lundia Ab Doped membranes

Similar Documents

Publication Publication Date Title
CN103706266B (en) In-situ polymerization micro-PVPP modified poly (ether-sulfone) hollow-fibre membrane and its production and use
CN103469362A (en) Porous polyethyleneimine and chitosan blend fiber and preparation method and applications thereof
WO2008071062A1 (en) A modified polyacrylonitrile fiber and its preparation process and use
CN102432782B (en) Amphiphilic triblock copolymer, preparation method thereof, and polyethersulfone hollow fiber membrane blend-modified by using amphiphilic triblock copolymer
CN103301759B (en) A kind of hollow polysulfone fiber dialysis membrane and manufacture method thereof
CN105268331B (en) A kind of preferable PVDF seperation films of blood compatibility and preparation method thereof
CN102961977A (en) Preparation method of polylactic-acid hollow fiber dialysis membrane
CN104005114B (en) A kind of preparation method of wool keratin regenerated celulose fibre
CN110743392B (en) PVDF hollow fiber membrane material with anticoagulation property for hemodialysis and preparation method thereof
CN109675134A (en) A kind of anticoagulant method of modifying of haemodialyser and its application
CN101396642A (en) Antibiotic hollow fiber separation film and preparation method thereof
CN106466562B (en) The preparation method of anticoagulation hemodialysis membrane
CN105879696A (en) High-hydrophilic internal pressure type polysulfone/sulfonate polysulfone hollow fiber ultrafiltration membrane and preparation method thereof
CN108752824A (en) A kind of preparation method of dialysis capillary fibers
CN110052187A (en) A kind of modified poly (ether-sulfone) and its preparation method and application
JPH0219204B2 (en)
CN105013355A (en) Heparan polyethersulfone hollow fiber membrane and preparation method and applications thereof
NO147979B (en) HOLE CELLULOSEDIA ACETATE FIBERS, PROCEDURES FOR MANUFACTURING THEREOF AND THEIR USE IN ARTIFICIAL Kidneys
JPH0451216B2 (en)
CN116966756A (en) Blood purifying membrane for removing proinflammatory cytokines and preparation method thereof
CN105544193A (en) Hydrophilic modification method for polyester fibers with bromoethane and PVA
CN105220245A (en) A kind of spinning solution of suitable electrospinning polytetrafluoroethylsuperfine superfine fiber film
CN109161987A (en) A kind of bionical wig fiber filament of sodium alginate/graphene and its preparation and application
CN108686520A (en) A kind of preparation method of hemodialysis membrane raw material
CN109316985B (en) Sulfonated dihydroxypropyl chitosan modified polyurethane hemodialysis membrane and preparation method thereof

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
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20181106

WD01 Invention patent application deemed withdrawn after publication