CN1027679C - Gas separation membrance with selective adsorbability - Google Patents
Gas separation membrance with selective adsorbability Download PDFInfo
- Publication number
- CN1027679C CN1027679C CN 89105555 CN89105555A CN1027679C CN 1027679 C CN1027679 C CN 1027679C CN 89105555 CN89105555 CN 89105555 CN 89105555 A CN89105555 A CN 89105555A CN 1027679 C CN1027679 C CN 1027679C
- Authority
- CN
- China
- Prior art keywords
- film
- membrane
- gas separation
- mentioned
- adsorbent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Images
Landscapes
- Separation Using Semi-Permeable Membranes (AREA)
Abstract
The present invention provides a gas separation membrane having a selective adsorption function, which belongs to the material of a separation membrane for mixed gases. The membrane material is prepared from additives composed of an adsorbing agent, metal powder or a solid catalyst, etc. and high molecular compounds which are blended. The membrane material of the present invention has excellent separation performance, and the separation coefficient alpha(H2/CO, H2/N2) of a porous membrane is higher than 3.74; the permeation rate is between J(H2) and 10+[-4] to 10+[-3] simultaneously or is even higher.
Description
The present invention relates to a kind of selection absorption property that has, be used for the film that mist separates, membrane material selects adsorbent, metal or metallic salt, the solid catalyst etc. of absorption property to make with high molecular polymer blend or reaction by having.
Membrane separation technique is with its efficient height, and technology is simple, and advantages such as small investment are applied to have tempting application prospect in the separation of various compounding substances increasingly extensively, and the separation that membrane separation technique is used for mist is the emphasis paid close attention to of people especially.
Problems such as the separation of mist and adjustment are the problems that industrial quarters extensively runs into.Along with industrial expansion, contain H
2, CO, CH
4Reasonable utilization Deng the industrial tail gas of composition is put in face of people day by day urgently.In the past, these tail gas or waste gas are difficult to be used economically except that being used for burning, cause the waste of resource and the pollution of environment, in recent decades, membrane separation technique is the development of membrane material particularly, for utilizing industrial tail gas that the possibility on the industry is provided, for example: from containing N
2Synthetic ammonia tailgas in separate to reclaim H
2And NH
3Deng.But in some field, the diffusion barrier The Application of Technology also has been subjected to some restrictions and difficulty.Whether these restrictions and difficulty be mainly from reasonable economically, that is, if the level of diffusion barrier technology does not reach the business accounting value of people's expectation, the application of this technology in this field will be very difficult.Undoubtedly, the separative efficiency of raising membrane material is the important channel that solves this difficult problem.
Usually, separation membrane material is divided into homogeneous membrane and perforated membrane two big classes.The infiltration mechanism of homogeneous membrane is dissolving-diffusion theory, and promptly gas at first in the absorption of film surface, dissolves then, and spreads from high side to low side in film, and last desorption comes out.In this process, what determine permeance property is the dissolution degree of gas with various molecule to membrane material, and therefore this mechanism is called as dissolving-diffusion mechanism.For perforated membrane, what determine permeance property is gas flow situation in the microporous layers, i.e. promise gloomy (Kundsen) stream, and it has determined infiltration rate and separation.That is to say that when system is under the interactional ideal case that can ignore intermolecular or molecule and hole wall etc., this film will equal the square root of the inverse of molecular weight ratio for the separation factor alpha (A/B) of mist so, promptly α (A/B)=
/
。For H
2/ CO, H
2/ N
2The desirable separation α of gaseous mixture equals
, be about 3.74.Obviously the above-mentioned theoretical treatment that perforated membrane is carried out and the agenda of film have bigger distance.Therefore, also there is not a kind of separation of perforated membrane to reach this theoretical value so far.
Find that through long term studies common polymeric membrane always is inverse relation to the permeability and the selectivity of certain gas.Promptly improve permeability, selectivity just reduces, otherwise, improving selectivity, permeability just reduces.Undoubtedly, there is the gas separation membrane of actual application value must possess high infiltration rate and high selectivity simultaneously, usually, homogeneous membrane has very high selectivity, and perforated membrane has higher infiltration rate, but be difficult to have both this 2 point with a kind of polymeric membrane, that is to say that you become a film at very difficult homogeneous membrane and perforated membrane " are done ", though you can make composite membrane to it.In order to improve traditional macromolecule permeability of the membrane and selectivity, people carry out copolymerization to two or more compound; Or blend; Or be prepared into composite membrane with ultra-thin active layer.Application with the developing membrane separation technique.
Virtuous controlled once publish an article [surface (day) 23, (1) 28(1985)] of the former paddy of Japan, proposition is used for C
1The performance objective value of the gas separation membrane of chemistry, promptly under the situation of the organic film of porous, working pressure is 50kg/cm
2More than, maximum operation (service) temperature is 150 ℃, its separating property (Capacity Ratio) H
2/ CO is 2～3, and transmission coefficient is 10
-4(cm
3Cm/cm
2CmHgsec) more than, in other words,, just has C if the performance of diffusion barrier reaches above-mentioned value under these conditions
1The possibility of chemical industry application.In addition, many remaining industrial departments, for example: synthetic ammonia PETROLEUM PROCESSING (reforming process etc.) and from natural gas, reclaiming. concentrate a large amount of hydrogen etc., all proposed corresponding requirement.
1987 United States Patent (USP) (US4,636,314) a kind of macromolecule that adds metal heteropoly acid or its salt and make in high molecular polymer and the blend film of inorganic matter are disclosed.1987 Japan Patent (JP62,202,801) a kind of metal dust that is full of adsorbable hydrogen in polymeric membrane () patent for example: palladium, platinum, nickel etc. is also disclosed.But above-mentioned patent is not all announced the chemical physical property and the master datas such as permeability and selectivity of relevant film.
1988 United States Patent (USP) (US4,740,219) disclose again a kind of in cellulose acetate, add special construction with hydrophobic grouping contain si molecular sieves Silicalite(Nature, Vol.271, Feb.9,1978, P512～516), as adsorbent.Become single phase film with solution-cast, this film is used for 02/N
2, CO
2/ H
2Separation, this film has bigger separation factor, but does not announce the master data of film seepage velocity J value in the patent, and the chemistry of film, physical property.Because concerning nonporous membrane, its separation factor alpha value will be far longer than perforated membrane.Therefore, to diffusion barrier, α value and J value have meaning of equal importance.
The objective of the invention is to utilize adsorbent. metal dust and its esters, solid catalyst is to the adsorption property (physical absorption of gas with various, chemisorbed, ADSORPTION STATE etc.), redox reaction performance and polymeric membrane are to the differential permeability of gas, a kind of gas separation membrane of selecting absorption property that has is provided, " behavior " of this film may not be subjected to " classics " film separation principle and theoretical restriction, this film is perforated membrane or nonporous membrane, is a kind of by adsorbent, metal, the single-phase mixture film of selecting the adsorbed gas function that has of catalyst etc. and macromolecular compound composition.
Another object of the present invention provides the above-mentioned method with gas separation membrane of selecting absorption property of preparation.
The 3rd purpose of the present invention is the above-mentioned film that makes to be used for membrane separator spare with practical value, for example H
2/ CO, H
2/ N
2, H
2/ CH
4, CO
2/ CH
4, O
2/ N
2Deng separation.
The present invention has the material of selecting adsorption function by adding in macromolecular compound, prepare separation membrane material.Worker of the present invention chances on, in macromolecular compound, add and have the prepared separation membrane of material of selecting adsorption function, have above-mentioned " classics " theoretical institutes inexplicable " behavior ", especially the separation factor alpha (A/B) of film (perforated membrane) is worth, surpassed the theoretical limiting value of these " classics ", and the separation factor alpha value is not only only relevant with the molecular weight of separated material, in other words, be exactly that the gas molecule of same molecular amount is when seeing through film of the present invention, have different speed, rather than " classics " theoretical said identical speed that has.This contribution of the present invention has not only improved the infiltration rate and the separation factor of gas separation membrane material greatly, and has opened up the approach for preparing the macromolecule gas separation membrane that the selection adsorption function is arranged with excellent properties.
The present invention utilizes Electronic Speculum, temperature programming adsorption/desorption technology. in-situ infrared technology, " process " of investigation gas permeation membrane material of the present invention.When proposing gas by film of the present invention, the ADSORPTION STATE that film had promotes conveyer mechanism.
As mentioned above, do not contain the perforated membrane of active additive, the principle of its separating mixed gas mainly is according to the gloomy molecular weight flooding mechanism of promise.The separation factor alpha of mist is only relevant with the molecular weight of gas molecule, promptly α (AB)=
/
。And we interpolation in the perforated membrane of certain adsorbent, find that but the α value has surpassed the limiting value of the gloomy theory of promise.Therefore, can confirm that its permeation mechanism is not only relevant with the gloomy diffuse flow of promise, and relevant with the situation of absorption, diffusion, desorption and ADSORPTION STATE, this point, we attempt to be illustrated in the following discussion.
The present invention utilizes film that macromolecular compound makes differential permeability energy and the physical and chemical performance thereof to gas with various, as: softening point, acid resistance, alkali resistance, dissolubility, viscosity, stretching, tearing strength and filming performance etc., selection can generate ADSORPTION STATE and adsorption bond strong and weak suitable metal dust, adsorbent, solid catalyst that oxidation-reduction reaction maybe can take place with separated gas molecule.Make the above-mentioned raw materials blend, fuse or be combined to one by chemistry or physical method, make macromolecule gas separation membrane with selection absorption property.
Above-mentioned metal dust is interpreted as the I in the 4th, 5,6 cycles, II, III, IV, V, VI, VII subgroup element and VIII family element in the periodic table of elements, for example: powder or its esters of Pt, Pd, Zn, Ag, Co, Ni, Nb, Fe, Cu, Cr, W, Mo etc.Adsorbent comprises various types of molecular sieves, for example: X type molecular sieve, A type molecular sieve, ZSM type molecular sieve, carbon molecular sieve etc., diatomite, silicon microballoon, aluminium oxide, and the various carriers (glazing of various models or not glazing carrier etc.) used of chromatography.Catalyst refers to the oxide catalyst that comprises above-mentioned metal or the metal/carrier catalyst that heterogeneous catalytic reaction is used, and these catalyst bases are generally SiO
2, AL
2O
3, SiO
2-Al
2O
3, ZnO, MgO and various types of molecular sieves etc.
A kind of or two or more above-mentioned adsorbent, metal dust or its esters or catalyst are in 2%～90%(weight) ratio and a kind of or two or more following organic high molecular polymer in 98%～10%(weight) ratio make through blend, fused or reaction and have the macromolecule gas separation membrane of selecting absorption property.
Above-mentioned macromolecular compound is meant organic silicon rubber, polyvinyl alcohol, cellulose acetate (two, three acetic acid), polysulfones, ethyl cellulose, polyacrylic acid, polyimides, NC Nitroncellulose etc., or the mixture of two or more above-mentioned macromolecular compound compositions.
Above-mentioned organic polymer is dissolved in the solvent with concentration in certain proportion, add (or not adding) suitable metal dust or its esters, adsorbent and solid catalyst, (temperature, mixing speed, humidity etc.) are mixed, are fused or reaction under certain conditions, obtain glue, this glue on clean smooth plate in air or in water casting film, perhaps use general film-forming apparatus film forming.Appropriate time then wears out in hot-air or hot water.
Above-mentioned glue also can be coated in to support on the ground and form composite membrane.
Above-mentioned mixing, fused or reaction condition are generally: 10～50 ℃ of temperature, mixing speed and time are with abundant mixing and reaction is advisable smoothly.
Above-mentioned membrance casting condition is, in air: temperature 5-40 ℃, relative temperature 30～90% is in the water: 0～50 ℃ of temperature, 0.1～5 minute time, the aging condition of film is in water: 50～90 ℃ of temperature, 1～8 hour time, the drying condition of film, in air: 20～80 ℃ of temperature, in a vacuum: 20～50 ℃ of temperature, 1～8 hour time.
Purpose of the present invention, can also realize by following manner:
By above-mentioned prescription and technology, adsorbent is the molecular sieve of carbon molecular sieve, sodium X type (13X) molecular sieve, calcium A type molecular sieve or other types, and macromolecular compound is ethyl cellulose, cellulose acetate or polysulfones.
Metal dust is cobalt powder or copper powder, and macromolecular compound is ethyl cellulose, cellulose acetate or polysulfones.
Adsorbent is active carbon and CuCl, and macromolecular compound is polysulfones or cellulose acetate.
Adsorbent is Pd/Al
2O
3Catalyst and CuCl, macromolecular compound are polysulfones.
Adsorbent can also select 13X(sodium X type) molecular sieve, macromolecular compound is polysulfones or cellulose acetate.
Adsorbent can also be 5A type (calcium A type) molecular sieve, and macromolecular compound is a cellulose acetate.
Adsorbent can also be to contain Na
2O, Al
2O
3Or SiO
2The equimolecular sieve, macromolecular compound is a cellulose acetate.
Solvent in the above-mentioned filming technology can be ketone, ester class, alcohols, amide-type and pyridine, oxolane, methyl-sulfoxide, dioxane etc., or the mixed liquor of two or more above-mentioned each kind solvents.
Above-mentioned support ground is meant, can make film increase the material of stretching, tearing strength, the present invention includes polyimides, polysulfones, polypropylene, polyester, nonwoven, cellulose family macromolecule etc.
The amount that joins metal dust in the above-mentioned macromolecular compound, adsorbent, solid catalyst is with 10～40%(weight) for good, wherein the ratio between metal dust, adsorbent, the solid catalyst can be regulated arbitrarily.
Adding the particle of additives such as metal dust in the film, adsorbent, solid catalyst to and be advisable with diameter 0.5～150 μ m, certainly, as not considering economic cause and changing the performance of additive, is good with fine grained.The surface area of these powder particles is 10～1500m
2/ g.The granular size of additive and distribution and specific area have direct relation, and for example mean particle size is 6 microns a reduced iron powder, and its specific surface can reach 5160m
2/ g.As the superfines of＜0.5 micron of selection, its specific surface may be bigger.As additive is porosity, and its average pore size is 1A～100 μ m.Under the prerequisite of keeping membrance casting condition and film-strength, the addition of additive can be unrestricted, but with 10～40%(weight) be good.The method that adds can directly be added in the glue, or adding also can behind the first soaked in solvent.Stirring the back powder particle can evenly or asymmetricly be distributed in the film.Powder particle also can add in film forming procedure, forms one deck additive powder bed on the surface of film.
From prior art and theory, we know that the thickness of diffusion barrier has a direct impact the transmitance of film, therefore, how to do film very thinly, to obtain bigger permeability, have become a kind of special technology.And the film made from prescription of the present invention and technology with very thick through what film was done, and does not influence the infiltration rate of film, is 1 * 10 with the thickness range of the film of above-mentioned prescription and method preparation
-3～0.5cm, we get rid of certainly, do film thinlyyer with prescription of the present invention and method, or thicker again, and adaptability of the present invention and uniqueness here just are described.
In above-mentioned filming technology, we can also select preferable condition.
In air, membrance casting condition is preferably: 20～35 ℃ of temperature, and relative humidity 40～60%, and in water: 0～35 ℃ of temperature, 0.5～4 minute time.The film that makes is worn out, the stability of film is very important, but should suits, aging under following condition is better choice: 60～90 ℃ of water temperatures, 1～3 hour time.Drying condition in the vacuum: 10～40 ℃ of temperature, 1～5 hour time.
The film made from above-mentioned prescription and method is porous or imporosity, is the single phase film with certain extension and tearing strength.
The permeability of above-mentioned film is at U.S. ASTM1434V(1975) carry out on the CS-135-241 type Permeability gauge recommended, assay method adopts modified constant voltage volumetric method, the 3400 gas chromatograph Analysis for CO, the O that produce with Varian company
2, N
2, H
2Deng component.
The performance of this film is: separating H
2/ CO, H
2/ N
2The time its separation α can be up to more than 3.0, even surpass 3.74 and reach 5.3, permeability J(H
2) [cm
3(STP)/cm
2SeccmHg]＞10
-4～10
-3
Of the present invention have a gas separation membrane of selecting absorption property, through temperature-programmed adsorption-desorption technology, in-situ infrared technology and transmission electron microscope, the determining adsorption instrument confirms that it can select to adsorb certain gas as O automatically
2, N
2, H
2, CO, CO
2, CH
4Reach gases such as rudimentary hydro carbons, and form ADSORPTION STATE on the surface, and the degree of stability of this ADSORPTION STATE, the size of adsorbance directly influences the permeability of the membrane energy.
Because film of the present invention has added " active particles " such as adsorbent, metal dust, solid catalysts, make that the surface of polymeric membrane is uneven, its existing catalytic activity application point, the adsorption activity application point is arranged again, the suction-operated of varying strength takes place between these application points and the gas molecule, and having formed ADSORPTION STATE, this ADSORPTION STATE has just played promotion conveying effect probably.
Accompanying drawing is Electronic Speculum (SEM) photo of diffusion barrier of the present invention, and macromolecular compound is a polysulfones, and additive is a solid catalyst, and wherein Fig. 1 and Fig. 2 are the surface of film, and Fig. 3 and Fig. 4 are the section (multiplication factor is respectively 1000 times and 2000 times) of film.Photo shows that there is more solid powder particle (white particle) film surface and inside.The section photo shows that the catalyst of interpolation has some and polysulfones to be bundled together, in some holes in the polysulfones porous layer.When gas with various saw through film, gas will contact with solid catalyst, adsorbent or metal dust inevitably, also just exists competitive Adsorption, diffusion, desorption, perhaps forms ADSORPTION STATE, has also just formed the peculiar penetration mechanism of film of the present invention.
The Carlo Erba 1822 type automatic absorbing analyzers that the present invention produces with Italy are measured adsorbent one polymeric membrane, and catalyst-polymeric membrane finds that their specific area and pore-size distribution and pore size are all different. And permeability of the membrane can (separation factor and infiltration rate) have direct relation with these data.
In sum, the present invention has outstanding substantive distinguishing features and significant technological progress compared with the prior art.
1, the master data of the prescription of film and film (such as specific area, pore-size distribution and pore size) shows, film has unique The Nomenclature Composition and Structure of Complexes.
2, film has excellent permeance property, shows that film possesses high selectivity (separation factor) and high infiltration rate simultaneously. Film is for separating of H2/CO、H
2/N
2During Deng gaseous mixture, J(H2) 10-4～10
-2In the scope, and α can be up to more than 3.0, even surpass 3.74 and reach 5.3.
3, owing to embedded active additive in the film, make film have simultaneously very high separation factor and infiltration rate, become possibility so that make thick film, thickness of the present invention can reach about 5mm.
For the present invention is described better, the invention will be further described by following embodiment:
Example 1
The 2g molecular sieve (contains Na
2O, Al
2O
3, SiO
2Deng) granularity is less than 0.1mm, joins in the dimethyl formamide solution of polysulfones, the mixture heating is stirred, and forms glue, is poured on the glass plate of level, and 20 ℃ of temperature, solvent flashing drying and forming-film in the air of relative temperature 50%, this film are perforated membrane.
Above-mentioned film is immersed the polysulfones solution some time, still dry under these conditions after the taking-up, become the film of post forming.After measured, the surface area of this film is 78.49m
2/ g, pore volume are 0.064cm
3/ g, pore volume are 0.064cm
3/ g, average pore radius is 16.6
, the infiltration rate J(H of film
2)＞10
-3, separation α (H
2/ CO)＞3.7, α (H
2/ N
2)＞3.0.
Example 2
Get the saturated CuCl dimethyl formamide solution of 4ml and polysulfones/dimethyl formamide solution of 16g20%, the stirring of suitably heating makes it molten entirely, adds 2gPd/Al again
2O
3Catalyst (granularity is less than 0.01mm) stirs, and leaves standstill a moment, and in the film forming on glass of level, surface area is 24.75m after measured then
2/ g, pore volume are 0.107cm
3/ g, average pore radius is 86.6A, this film is used to separate H
2/ CO, H
2/ N
2, its infiltration rate J(H
2)＞10
-3, separation factor alpha＞3.1.
Example 3
Get ethyl cellulose (ethyoxyl content 45～47%) and be dissolved in following solvent: ethanol, butanone, oxolane, pyridine, butyl acetate, dioxane, its concentration are 1～15%(weight), in film forming (under room temperature) on the flat board of level or on the polyester film, vacuum drying five hours makes nonporous membrane.But above-mentioned glue also coated is made composite membrane on backing material, for example, and nonwoven, porous polypropylene nitrile, or the porous PS membrane etc.
By above-mentioned prescription and method, in glue, add an amount of plasticizer (as: triethyl phosphate, tributyl phosphite, butyl phthalate, diethyl phthalate, butyl borate, three diglycol ethylenes, glyceryl triacetate, PEG400 etc.), can increase substantially the infiltration rate of film.
Example 4
Getting 15g concentration is 4～7%(weight) the pyridine solution of ethyl cellulose (ethyoxyl content 45～47%), add 1g cobalt powder (granularity is less than 200 orders), film forming on the glass plate of level is leached film in the water, again at 30～50 ℃ of following vacuum drying 5 hours, its seepage velocity J(H
2)＞10
-4, J(CO)＞10
-4, α (H
2/ CO)＞3.5, α (H
2/ N
2)＞3.5.
Example 5
Granularity (contains Na less than the molecular sieve of 0.10mm
2O, Al
2O
3, SiO
2Deng) 1g, joining in the dimethyl formamide solution of cellulose acetate and go, mixture suitably heats, stirs, forms glue, suitably leaves standstill, and at room temperature film forming makes perforated membrane, after tested, infiltration rate J(H
2)＞10
-2, J(CO)＞10
-3, separation factor alpha (H
2/ CO)＞3.2, α (H
2/ N
2)＞3.5.
Example 6
By example 5 prescription and preparation methods, replace cellulose acetate, the infiltration rate J(H of the perforated membrane that makes with ethyl cellulose
2)＞10
-2, α (H
2/ N
2)＞3.5.
Example 7
The adsorbent molecular sieve of carbon molecular sieve, sodium X type (13X) molecular sieve or other types, granularity is less than 0.10mm, molten the going of dimethyl formamide that joins the pyridine solution of ethyl cellulose or cellulose acetate, polysulfones gone in the liquid, mixture heats, stirs, leaves standstill, on the glass plate, on the metal film tool or on the polyester film, solvent flashing under 20～30 ℃ of air of temperature, dry under vacuum or the room temperature, make perforated membrane.
Change above-mentioned each molecular sieve analog into all kinds of solid catalysts,, also can be made into the perforated membrane of excellent performance as metal/carrier, metal oxide etc.
Example 8
1 gram molecule sieve (siliceous, granularity is less than 0.1mm) adds dimethyl formamide 9 grams, stirs 3 hours, the dimethyl formamide solution that adds cellulose acetate, stir, remove bubble, be poured over (27 ℃ of temperature on the smooth clean water flat glass plate, air pressure 630mmHg), striking film forming 2-3 minute dropped in the water 2-3 minute immediately, again this film drop in 85 ℃ the hot water 1 hour aging, take out the back film is blotted, and air dry is promptly under the smooth condition of film.This film J(H
2)=4.40 * 10
-4, J(N
2)=9.09～9.27 * 10
-5, α (H
2/ N
2)=4.84～5.25.
Example 9
Granularity is less than copper powder (crossing with hydrogen reducing in advance) 1 gram of 0.05mm, joining the dimethyl formamide of polysulfones or cellulose acetate goes in molten, mixture suitably heats, stir, form glue, suitably leave standstill, film forming at room temperature, aging in hot-air or hot water, make gas separation membrane, after tested infiltration rate J(H
2) be 5.2 * 10
-4, α (H
2/ CO)=3.8, α (H
2/ N
2)=3.6.
Example 10
Getting CuCl solution is soaked in the active carbon, dry again, activation, make the active carbon that contains CuCl,, join in the dimethyl formamide solution of polysulfones or cellulose acetate and go this active carbon 1 gram, suitably heating, stir, form glue, remove bubble, under the room temperature on the clean glass plate of level film forming, air dry.The infiltration rate of this film is: J(H
2)=2.32 * 10
-2, J(N
2)=6.37 * 10
-3, J(CO)=6.35 * 10
-3, J(CO
2)=4.91 * 10
-3, separation factor is: α (H
2/ N
2)=3.64, α (H
2/ CO)=3.65.
The infiltration rate unit that this paper mentions is: cm
3(STP)/cm
2SeccmHg.
Best enforcement just is example 1, example 8, example 9, example 10.
Claims (7)
1, has the macromolecule gas separation membrane of selecting absorption property, the following macromolecular compound that it is characterized in that the additive be made up of one or more following metallic salts, adsorbent, the solid catalyst of 2%-90% (weight) and 98%-10% is through blend, and fused or reaction is made;
Above-mentioned metallic salt comprises nitrate and the chloride of Co, Cu, Cr;
Above-mentioned solid catalyst is meant Fe-Cr-Zn, P-Mo-Bi oxide catalyst and Pt/Al
2O
3, Pd/Al
2O
3, Pd-Pt/Al
2O
3Metal/carrier catalyst;
Above-mentioned adsorbent is the active carbon that soaked above-mentioned slaine;
Above-mentioned macromolecular compound is cellulose diacetate, polysulfones, ethyl cellulose.
2, gas separation membrane as claimed in claim 1 is characterized in that adsorbent is CuCl, and solid catalyst is Pd/Al
2O
3, Pt/Al
2O
3, macromolecular compound is a polysulfones.
3, gas separation membrane as claimed in claim 1 is characterized in that metallic salt is Cu(NO
3)
2, solid catalyst is Pt/Al
2O
3, macromolecular compound is a cellulose diacetate.
4, gas separation membrane as claimed in claim 1 is characterized in that solid catalyst is Fe-Cr-Zn or P-Mo-Bi oxide catalyst, and macromolecular compound is a polysulfones.
5, gas separation membrane as claimed in claim 1, the particle that it is characterized in that adsorbent, solid catalyst is 0.5-150 μ m or thinner, surface area is 10-1500m
2/ g or bigger, average pore size is 1A-100 μ m.
6, as gas separation membrane as described in the claim 5, it is characterized in that thickness is 1 * 10
-3-0.5cm.
7,, it is characterized in that film is perforated membrane or nonporous membrane as claim 5 or 6 described gas separation membranes.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 89105555 CN1027679C (en) | 1989-08-10 | 1989-08-10 | Gas separation membrance with selective adsorbability |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 89105555 CN1027679C (en) | 1989-08-10 | 1989-08-10 | Gas separation membrance with selective adsorbability |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1040152A CN1040152A (en) | 1990-03-07 |
| CN1027679C true CN1027679C (en) | 1995-02-22 |
Family
ID=4856259
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 89105555 Expired - Fee Related CN1027679C (en) | 1989-08-10 | 1989-08-10 | Gas separation membrance with selective adsorbability |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1027679C (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100368355C (en) * | 2005-08-15 | 2008-02-13 | 中国石油化工股份有限公司 | Method for raising yield of ethene, propylene |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5824617A (en) * | 1994-07-08 | 1998-10-20 | Exxon Research & Engineering Company | Low alkaline inverted in-situ crystallized zeolite membrane |
| US5672388A (en) * | 1994-07-08 | 1997-09-30 | Exxon Research & Engineering Company | Membrane reparation and poer size reduction using interfacial ozone assisted chemical vapor deposition |
| US5871650A (en) * | 1994-07-08 | 1999-02-16 | Exxon Research And Engineering Company | Supported zeolite membranes with controlled crystal width and preferred orientation grown on a growth enhancing layer |
| CN1309461C (en) * | 2004-01-13 | 2007-04-11 | 中国科学院生态环境研究中心 | Acetyl cellulose/Fe-Al oxide composite membrane, and its preparing method and use |
| CN101518719B (en) * | 2008-02-29 | 2012-02-01 | 中国科学院过程工程研究所 | Method for preparing organic-inorganic hybrid evaporation alcohol permselective membrane |
| US8440000B2 (en) * | 2010-01-22 | 2013-05-14 | Board Of Trustees Of Leland Stanford Junior University | Nitrogen-permeable membranes and uses thereof |
| CN103665531A (en) * | 2013-11-11 | 2014-03-26 | 深圳职业技术学院 | Plastic porous material and preparation method thereof |
| CN105457501B (en) * | 2015-12-19 | 2018-01-05 | 杭州水处理技术研究开发中心有限公司 | A kind of preparation method of efficient gas seperation film |
| CN109173752B (en) * | 2018-09-10 | 2021-10-01 | 杭州博大净化设备有限公司 | Mixed matrix membrane for gas separation and preparation method thereof |
| CN109529641B (en) * | 2019-01-11 | 2021-04-20 | 天津工业大学 | Polyimide-photosensitive cobalt organic framework hybrid membrane preparation and gas separation application |
| CN114749145B (en) * | 2022-04-28 | 2023-07-18 | 东北石油大学 | Molecular sieve for adsorption separation of nitrogen and methane and preparation method thereof |
| CN117695869B (en) * | 2024-02-02 | 2024-04-19 | 天津工业大学 | Iron-based alloy hollow fiber membrane for hydrogen separation and preparation method thereof |
-
1989
- 1989-08-10 CN CN 89105555 patent/CN1027679C/en not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100368355C (en) * | 2005-08-15 | 2008-02-13 | 中国石油化工股份有限公司 | Method for raising yield of ethene, propylene |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1040152A (en) | 1990-03-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN1027679C (en) | Gas separation membrance with selective adsorbability | |
| EP1372832B1 (en) | Flexible and porous membranes and adsorbents, and method for the production thereof | |
| Shah et al. | Pervaporation of alcohol–water and dimethylformamide–water mixtures using hydrophilic zeolite NaA membranes: mechanisms and experimental results | |
| AU636703B2 (en) | Controlled pore composite polytetrafluoroethylene article and method therefor | |
| EP1468718B1 (en) | Air filter unit with several filtering media | |
| CN108201878B (en) | Preparation method of carbon-point-modified metal organic framework adsorption material and application of carbon-point-modified metal organic framework adsorption material in treatment of water pollutants | |
| US8337601B2 (en) | Air filter sheet, process for manufacturing same, and air filter | |
| CN103958027A (en) | Methods of applying a sorbent coating on a substrate, a support, and/or a substrate coated with a support | |
| HUT66847A (en) | Particle-loaded nonwoven fibrous article for separations and purifications | |
| CN108816058B (en) | Emodin molecular imprinting titanium dioxide nano particle composite membrane and preparation method and application thereof | |
| KR101402604B1 (en) | Metal-Complexed carbon Menmbrane and method for preparing the same | |
| CN104226256A (en) | Spherical forming Cu base metal organic skeleton-graphene oxide composite material and preparation method of spherical forming Cu base metal organic skeleton-graphene oxide composite material | |
| US9610561B2 (en) | Method of making a honeycomb having channels containing a porous adsorbent | |
| CN102120179A (en) | Preparation method of modified activated carbon fiber for adsorbing ultra-micro sulfur dioxide | |
| CN105797596B (en) | A kind of preparation method of filter membrane for Water warfare | |
| CN107952289A (en) | A kind of filter screen with purifying formaldehyde and preparation method thereof | |
| CN114797799A (en) | Preparation method of MOFs-based lithium ion imprinting composite nanofiber membrane | |
| CN112705179A (en) | Hierarchical different-pore covalent organic framework material and preparation method and application thereof | |
| CN101007270B (en) | Composite material of micro-fiber encapsulated active carbon or active carbon catalyst and preparation method thereof | |
| CN1027680C (en) | Catalytic-polymeric gas separation membrane | |
| CN109663564A (en) | A kind of gas adsorption material and preparation method thereof | |
| CN111589428A (en) | Composite material for purifying air and preparation method thereof | |
| CN110624398B (en) | Air purification composite material | |
| CN109248653A (en) | A kind of gas adsorption material and preparation method thereof | |
| CN113423485B (en) | Filter medium for depositing nitrogen oxides |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| C19 | Lapse of patent right due to non-payment of the annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |