TRAN HOWIE Q (US)
| WO2015047702A1 | 2015-04-02 |
| US8613362B2 | 2013-12-24 | |||
| US20150165383A1 | 2015-06-18 | |||
| US5762798A | 1998-06-09 |
| CLAIMS: 1. A polyimide polymer comprising a plurality of repeating units of formula (I): wherein Xi is selected from the group consisting of and mixtures t ereo; w eren X2 s seecte rom t e group consstng o and mixtures thereof; Yi is selected from the group consisting and mi and mixtures thereof, and -Ri is selected from the group consisting of -H, -COCH3, \ HN \ -CH2 H7C: (R20)3Si- and mixtures thereof, and -R2 is selected from the group consisting of -CH3, -C2H5 and-R3 is selected from the group consisting of and mixtures thereof; n and m are independent integers from 2 to 500; the molar ratio of n/m is in a range of 1 : 10 to 10: 1. 2. The polyimide polymer of claim 1 wherein Xi and X2 are the same and are 3. The polyimide polymer of claim 1 wherein Y\ is 4. The polyimide polymer of claim 1 wherein Y2 is and-Ri is selected from the group consistin of 5. A polyimide polymer membrane comprising the polyimide polymer of any of claims 1-4. 6. The polyimide polymer membrane of claim 5 is chemically and UV cross-linked. 7. The polyimide polymer membrane of claim 5 comprising a thin nonporous selective separation layer formed from the polyimide polymer with a plurality of repeating units of formula (I) and a porous nonselective mechanical support layer made from a material different from the polyimide polymer with a plurality of repeating units of formula (I). 8. A method of making a chemically and UV cross-linked polyimide membrane comprising: 1) preparing a casting solution of a polyimide polymer with a plurality of repeating units of a formula (I): wherein Xi is selected from the group consisting of and mixtures thereof; wherein X2 is selected from the group consisting of and mixtures thereof; Yi is selected from the rou consistin and mixtures thereof Y2 is selected from the group consistin of and mixtures thereof, and -Ri is selected from the group consisting of -H, -COCH 3> o HN -CH-, H2C; -CH, (R20)3Si- and mixtures thereof, and -R2 is selected from the group consisting -CH3, -C2H5 and-R3 is selected from the group consisting of and mixtures thereof; n and m are independent integers from 2 to 500; the molar ratio of n/m is in a range of 1 : 10 to 10: 1 by: a) dissolving 3-isocyanatopropyltrialkyloxysilane and a polyimide polymer with a plurality of repeating units of formula (II) wherein Xi is selected from the group consisting of and mixtures thereof; wherein X2 is selected from the group consisting of and mixtures thereof; Yi is selected from the group consisting and mixtures thereof; Y3 is selected from the group consisting of and mixtures thereof, and -R4 is selected from the group consisting of -H, -COCH3, and mixtures thereof, and-R.5 is selected from the group consisting of and mixtures thereof; n and m are independent integers from 2 to 500; the molar ratio of n/m is in a range of 1 : 10 to 10 in an organic solvent to form a homogeneous solution; b) heating said homogeneous solution for 4-8 hours at 40-70°C to form said solution of the polyimide polymer via a reaction between 3-isocyanatopropyltrialkyloxysilane and said polyimide polymer with a plurality of repeating units of formula (II); 2) casting said casting solution of the polyimide polymer with a plurality of repeating units of formula (I) on a membrane substrate or on a polymeric cloth substrate or on a clean glass plate to form a thin layer of said casting solution of the polyimide polymer with a plurality of repeating units of formula (I); 3) removing the organic solvents from the thin layer of said casting solution of the polyimide polymer to form a flat sheet membrane;4) drying the membrane to form chemically cross-linked polyimide membrane comprising the polyimide polymer with a plurality of repeating units of formula (I) wherein the trialkyloxysilane groups have reacted with each other and have formed covalent bonds among the polymer chains; 5) coating said dried membrane with a thin layer of high permeability material; and 6) UV cross-linking said coated and dried membrane via UV radiation to cross-link the membrane via covalent bonds between the UV cross-linkable sulfonyl or carbonyl group and methyl group on said new polyimide polymer chains with a plurality of repeating units of formula (I). 9. A process for separating at least one gas from a mixture of gases using a high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross- linked polyimide membrane the process comprising: (a) providing a both chemically and UV cross-linked polyimide membrane prepared from a polyimide polymer with a plurality of repeating units of a formula (I): wherein Xi is selected from the group consisting of and mixtures thereof; wherein X2 is selected from the group consisting and mixtures thereof; Yi is selected from the group consisting of and mixtures thereof Y2 is selected from the group consisting of and mixtures thereof, and -Ri is selected from the group consisting of -H, -COCH3, \ HN \ H2C^CH2 (R20)3Si^CH2 and mixtures thereof, and -R2 is selected from the group consisting of -CH3, -C2H5 and-R3 is selected from the rou consistin of and mixtures thereof; n and m are independent integers from 2 to 500; the molar ratio of n/m is in a range of 1 : 10 to 10: 1 wherein said polyimide membrane is permeable to said at least one gas; (b) contacting the mixture on one side of the polyimide membrane to cause said at least one gas to permeate the membrane; and (c) removing from the opposite side of the membrane a permeate gas composition comprising a portion of said at least one gas which permeated said membrane. 10. The process of claim 9 wherein said gases comprise volatile organic compounds in air, a mixture of helium, carbon dioxide or hydrogen sulfide in natural gas, . hydrogen in a mixture of hydrocarbon gases from a refinery or a mixture of olefins and paraffins. |
POLYIMIDE MEMBRANES FOR GAS SEPARATIONS
STATEMENT OF PRIORITY
[0001] This application claims priority to U.S. Provisional Application No. 62/184537 which was filed June 25, 2015, the contents of which are hereby incorporated by reference in its entirety.
BACKGROUND OF THE INVENTION
[0002] Membrane-based technologies have advantages of both low capital cost and high- energy efficiency compared to conventional separation methods. Polymeric membranes have proven to operate successfully in industrial gas separations such as in the separation of nitrogen from air and the separation of carbon dioxide from natural gas. Cellulose acetate (CA) is a polymer currently being used in commercial gas separation. For example, UOP LLC's Separex™ CA membrane is used extensively for carbon dioxide removal from natural gas. Nevertheless, while they have experienced commercial success, CA membranes still need improvement in a number of properties including selectivity, permeability, chemical and thermal stability. Natural gas often contains substantial amounts of heavy hydrocarbons, aromatics, and water, either as an entrained liquid, or in vapor form, which may lead to condensation within membrane modules. The gas separation capabilities of polymeric membranes are affected by contact with liquids including hydrocarbons and water. The presence of more than modest levels of hydrogen sulfide, especially in conjunction with water and heavy hydrocarbons, is also potentially damaging. Therefore, precautions must be taken to remove the entrained liquid water and heavy hydrocarbons upstream of the membrane separation steps. Another issue of polymeric membranes that still needs to be addressed for their use in gas separations is the plasticization of the polymer by condensable gases such as carbon dioxide and propylene that leads to swelling of the membrane as well as a significant increase in the permeability of all components in the feed and a decrease in the selectivity of the membranes. For example, the permeability coefficient of CO2 in polymeric membranes begins to increase when the pressure is above a certain level due to the onset of plasticization by the CO2. A high concentration of sorbed CO2 leads to increased segmental motion, and, consequently, the transport rate of the penetrant is enhanced. The challenge of treating gas, such as natural gas, that contains relatively large amounts of CO2, such as more than 50%, is particularly difficult.
[0003] Polymeric membrane materials have been found to be useful in gas separations. Numerous research articles and patents describe polymeric membrane materials (e.g., polyimides, polysulfones, polycarbonates, polyethers, polyamides, polyarylates,
polypyrrolones, etc.) with desirable gas separation properties, particularly for use in oxygen/nitrogen separation (See, for example, US 6,932,589). The polymeric membrane materials are typically used in processes in which a feed gas mixture contacts the upstream side of the membrane, resulting in a permeate mixture on the downstream side of the membrane with a greater mole fraction of one of the components than the composition of the original feed gas mixture. A pressure differential is maintained between the upstream and downstream sides, providing the driving force for permeation. The downstream side can be maintained as a vacuum, or at any pressure below the upstream pressure.
[0004] The membrane performance is characterized by the flux of a gas component across the membrane. This flux can be expressed as a quantity called the permeability (P), which is a pressure- and thickness-normalized flux of a given component. The separation of a gas mixture is achieved by a membrane material that permits a faster permeation rate for one component (i.e., higher permeability) over that of another component. The efficiency of the membrane in enriching a component over another component in the permeate stream can be expressed as a quantity called selectivity. Selectivity can be defined as the ratio of the permeabilities of the gas components across the membrane (i.e., PA/PB' where A and B are the two components). A membrane's permeability and selectivity are material properties of the membrane material itself, and thus these properties are ideally constant with feed pressure, flow rate and other process conditions. However, permeability and selectivity are both temperature-dependent. It is desired to develop membrane materials with a high selectivity (efficiency) for the desired component, while maintaining a high permeability (productivity) for the desired component. [0005] The relative ability of a membrane to achieve the desired separation is referred to as the separation factor or selectivity for the given mixture. There are however several other obstacles to use of a particular polymer to achieve a particular separation under any sort of large scale or commercial conditions. One such obstacle is permeation rate. One of the components to be separated must have a sufficiently high permeation rate at the preferred conditions or else extraordinarily large membrane surface areas are required to allow separation of large amounts of material. Another problem that can occur is that at conditions where the permeability is sufficient, such as at elevated temperatures or pressures, the selectivity for the desired separation can be lost or reduced. Another problem that often occurs is that over time the permeation rate and/or selectivity is reduced to unacceptable levels. This can occur for several reasons. One reason is that impurities present in the mixture can over time clog the pores, if present, or interstitial spaces in the polymer. Another problem that can occur is that one or more components of the mixture can alter the form or structure of the polymer membrane over time thus changing its permeability and/or selectivity. One specific way this can happen is if one or more components of the mixture cause plasticization of the polymer membrane. Plasticization occurs when one or more of the components of the mixture act as a solvent in the polymer often causing it to swell and lose its membrane properties. It has been found that polymers such as cellulose acetate and polyimides which have particularly good separation factors for separation of mixtures comprising carbon dioxide and methane are prone to plasticization over time thus resulting in decreasing performance of these membranes.
[0006] Some new high-performance polymers such as new polyimides (Pis), poly (trimethylsilylpropyne) (PTMSP), and polytriazole exhibit high ideal selectivities for CO2 over CH4 when measured with pure gases at modest pressures in the laboratory. However, the selectivity obtained under mixed gas, high pressure conditions is much lower than the calculated ideal level. In addition, gas separation processes based on glassy solution-diffusion membranes frequently suffer from plasticization of the stiff polymer matrix by the sorbed penetrant molecules such as CO2 or C3H6. Plasticization of the polymer represented by the membrane structure swelling and a significant increase in the permeabilities of all components in the feed occurs above the plasticization pressure when the feed gas mixture contains condensable gases.
[0007] Thus, there is a critical need for new high-performance membranes that will provide and maintain adequate performance under conditions of exposure to organic vapors or liquids, high concentrations of acid gases such as CO2 and hydrogen sulfide, and water vapor that are commonplace in natural gas treatment.
[0008] Conventional methods for stabilizing polymeric membranes involve either annealing or cross-linking. Cross-linking is a useful method to suppress the polymer membrane plasticization. Polymer membrane cross-linking methods include thermal treatment, radiation, chemical cross-linking, and UV-photochemical processes. Cross-linking offers the potential to improve the mechanical and thermal properties of a membrane. Cross- linking can be used to increase membrane stability in the presence of aggressive feed gases and to simultaneously reduce plasticization of the membrane. Normally, cross-linked polymer membranes have a high resistance to plasticization, but their other properties such as permeability and selectivity are much less than desired.
[0009] US 2005/0268783 Al disclosed chemically cross-linked polyimide hollow fiber membranes prepared from a monoesterified polymer followed by final cross-linking after hollow fiber formation.
[0010] US 7,485,173 disclosed UV cross-linked mixed matrix membranes via UV radiation. The cross-linked mixed matrix membranes comprise microporous materials dispersed in the continuous UV cross-linked polymer matrix.
[0011] US 8,337,598 disclosed a thin film composite hollow fiber membrane with a core layer and a UV-crosslinked polyimide polymer sheath layer.
[0012] Even after cross-linking of conventional polymers in accordance with the state of the art prior to the current invention, there has remained a need to improve the selectivity and permeability of the resulting membranes.
[0013] The present invention provides a new type of high selectivity, high plasticizati on- resistant and solvent-resistant, both chemically and UV cross-linked polyimide membranes. SUMMARY OF THE INVENTION
[0014] This invention discloses a composition of, a method of making, and applications of a new type of high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membranes.
[0015] Two main issues for traditional polymeric membranes are relatively low selectivities and plasticization of the polymers by condensable gases such as carbon dioxide and propylene that leads to swelling of the membrane as well as a significant increase in the permeability of all components in the feed and a decrease in the selectivity of the membranes. The present invention discloses a new type of both chemically and UV cross-linked polyimide membranes that have shown high selectivities and also extremely high
plasticization resistance to condensable gases such as CO2 and propylene for gas separations.
[0016] As an example, single-gas experimental results demonstrated that the both UV physically cross-linked and 3-isocyanatopropyltriethoxysilane chemically cross-linked poly(3,3',4,4'-diphenylsulfone tetracarboxylic dianhydride (DSDA)-3,3',5,5'-tetramethyl- 4,4'-methylene dianiline (TMMDA)-3,3'-dihydroxy-4,4'-diamino-biphenyl (HAB)) polyimide polymeric membrane described in this invention showed no plasticization induced by CO2 condensable gas up to 700 psig C0 2 partial pressure for CO 2 /CH 4 separation. The new membrane also showed high selectivities ( co2/CH4 = 42.5, am/cm = 245.9, aHe/CH4 = 243.4) and permeabilities (Pco 2 = 7.22 Barrers, P H2 = 41.8 Barrers, P He = 41.4 Barrers) for CO2/CH4, H2/CH4, and He/CH 4 separations.
[0017] This new type of high selectivity, high plasticization-resistant and solvent- resistant, both chemically and UV cross-linked polyimide membranes are highly promising for a variety of gas separations such as separations of H2/CH4, He/CF , CO2/CH4, CO2/N2, olefin/paraffin separations (e.g. propylene/propane separation), O2/N2, iso/normal paraffins, polar molecules such as H2O, H2S, and NH3 mixtures with CH4, N2, ¾, and other light gases separations. DETAILED DESCRIPTION OF THE INVENTION
[0018] Current polymeric membrane materials have reached a limit in their productivity- selectivity trade-off relationship for separations. Another issue is that gas separation processes based on glassy solution-diffusion membranes frequently suffer from plasticization of the stiff polymer matrix by the sorbed condensable penetrant molecules such as CO2 or C3H6. Plasticization of the polymer is exhibited by swelling of the membrane structure and a significant increase in the permeabilities for all components in the feed occurs above the plasticization pressure when the feed gas mixture contains condensable gases.
[0019] For example, for a cellulose acetate membrane, the high solubility of CO2 swells the polymer to such an extent that intermolecular interactions are disrupted. As a result, mobility of the acetyl and hydroxyl pendant groups, as well as small-scale main chain motions, would increase thereby enhancing the gas transport rates. This result indicates a strong need to develop new plasticization-resistant membrane materials. The markets for membrane processes could be expanded considerably through the development of robust, high plasticization-resistant membrane materials.
[0020] Conventional methods for stabilizing the polymeric membranes against plasticization are either annealing or cross-linking. Polymeric membrane cross-linking methods include thermal treatment, radiation, chemical cross-linking, UV-photochemical, blending with other polymers, etc.
[0021] This invention relates to a new type of high selectivity, high plasticization- resistant and solvent-resistant, both chemically and UV cross-linked polyimide membranes. More specifically, this invention relates to a method for making these novel high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membranes. This invention also pertains to the applications of these high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross- linked polyimide membranes for a variety of gas separations such as separations of
CO2/CH4, H2/CH4, He/CFLj, CO2/N2, olefin/paraffin separations (e.g. propylene/propane separation), O2/N2, iso/normal paraffins, polar molecules such as H2O, H2S, and
NH3/mixtures with CH4, N2, ¾, and other light gases separations. [0022] The new type of high selectivity, high plasticization-resistant and solvent- resistant, both chemically and UV cross-linked polyimide membranes described in the present invention is formed from a new polyimide polymer with a plurality of repeating units of formula (I):
wherein X 1 is selected from the group consisting of
and mixtures thereof; wherein X 2 is selected from the group consisting of
and mixtures thereof; Y is selected from the group consisting of
and mixtures thereof; Y 2 is selected from the group consisting of
and mixtures thereof, and -Ri is selected from the group consisting of
-H, -COCH 3 , \
HN
\
H C ^CH 2
(R 2 0) 3 Si^ CH2
and mixtures thereof, and -R 2 is selected from the group consisting
-CH3, -C2H5 and -R 3 is selected from the group consisting of
and mixtures thereof; n and m are independent integers from 2 to 500; the molar ratio of n/m is in a range of 1 : 10 to 10: 1.
[0023] Within formula (I), preferably Xi and X2 are the same following group
preferably preferably Y2 is
-Ri is selected from the group consisting of
and preferably -R 2 is
CH2CH3
[0024] The new polyimide polymer with a plurality of repeating units of formula (I) that is used for making the high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane described in the current invention have a weight average molecular weight in the range of 50,000 to 1,000,000 Daltons, preferably between 70,000 to 500,000 Daltons.
[0025] The high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane in the present invention can be either asymmetric integrally skinned membrane or thin film composite (TFC) membrane.
[0026] The high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane described in the present invention can be fabricated into any convenient geometry such as flat sheet (or spiral wound), tube, or hollow fiber.
[0027] The asymmetric integrally-skinned flat sheet or hollow fiber high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membranes in the present invention was prepared by a phase inversion process, and then by applying a thin coating layer on the surface of the membrane. [0028] The present invention provides a method for the preparation of high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane including: 1) preparing a casting solution of the new polyimide polymer with a plurality of repeating units of formula (I) by: a) dissolving 3- isocyanatopropyltrialkyloxysilane such as 3-isocyanatopropyltriethoxysilane and a polyimide polymer with a plurality of repeating units of formula (II) in an organic solvent such as N- methyl-2-pyrrolidone ( MP), 1,3-dioxolane, tetrahydrofuran (THF), and cyclohexanone to form a homogeneous solution; b) heating said homogeneous solution for 4-8 hours at 40- 70°C to form said solution of the new polyimide polymer with a plurality of repeating units of formula (I) via the reaction between 3-isocyanatopropyltrialkyloxysilane and polyimide polymer with a plurality of repeating units of formula (II); c) in some cases, some organic solvents such as hexane, n-octane, and n-decane that cannot dissolve the new polyimide polymer with a plurality of repeating units of formula (I) are added to said casting solution; 2) casting said casting solution of the new polyimide polymer with a plurality of repeating units of formula (I) on a membrane substrate or on a polymeric cloth substrate or on a clean glass plate to form a thin layer of said casting solution of the new polyimide polymer with a plurality of repeating units of formula (I); 3) removing the organic solvents from the thin layer of said casting solution of the new polyimide polymer with a plurality of repeating units of formula (I) to form a flat sheet membrane; 4) drying the membrane to form the chemically cross-linked polyimide membrane comprising the new polyimide polymer with a plurality of repeating units of formula (I) wherein the trialkyloxysilane groups have reacted with each other and have formed covalent bonds among the polymer chains; 5) coating said dried membrane with a thin layer of high permeability material such as a fluoropolymer or a UV radiation curable epoxy silicone; and 6) UV cross-linking said coated and dried membrane via UV radiation to further cross-link the membrane via covalent bonds between the UV cross-linkable sulfonyl or carbonyl group and methyl group on said new polyimide polymer chains with a plurality of repeating units of formula (I) to form said high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane. [0029] The polyimide polymer used for the synthesis of the new polyimide polymer with a plurality of repeating units of formula (I) has a plurality of repeating units of formula (II):
wherein X 1 is selected from the group consisting of
and mixtures thereof wherein X 2 is selected from the group consisting
and mixtures thereof; Y 1 is selected from the group consisting of
and mixtures thereof; Y 3 is selected from the group consisting of and mixtures thereof, and -R4 is selected from the group consisting of -H, -COCH 3 , and mixtures thereof, and -R 5 is selected from the group consisting of
and mixtures thereof; n and m are independent integers from 2 to 500; the molar ratio of n/m is in a range of 1 : 10 to 10: 1.
[0030] Within formula (II), preferably Xi and X2 are the same following group
preferably Yi is
preferably Y3 is
preferably -R4 is a mixture of -H and -COCH 3 .
[0031] The polyimide polymer with a plurality of repeating units of formula (II) that is used for synthesis of the new polyimide polymer with a plurality of repeating units of formula (I) described in the current invention have a weight average molecular weight in the range of 50,000 to 1,000,000 Daltons, preferably between 70,000 to 500,000 Daltons.
[0032] The thin film composite high selectivity, high plasticization-resistant and solvent- resistant, both chemically and UV cross-linked polyimide membrane described in the current invention comprises a thin nonporous selective separation layer formed from the new polyimide polymer with a plurality of repeating units of formula (I) described in the present invention and a porous nonselective mechanical support layer made from a material different from the new polyimide polymer with a plurality of repeating units of formula (I) described in the present invention. The thin film composite high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane described in the current invention has either hollow fiber or flat sheet geometry.
[0033] The porous nonselective mechanical support layer was made from a material different from the new polyimide polymer with a plurality of repeating units of formula (I) described in the present invention with a low selectivity and high flux. Selection of the porous nonselective mechanical support layer for the preparation of TFC high plasticizati onresistant and solvent-resistant polymeric membrane in the present invention may be made on the basis of the heat resistance, solvent resistance, and mechanical strength of the porous nonselective mechanical support layer, as well as other factors dictated by the operating conditions for selective permeation. The porous nonselective mechanical support layer is preferably at least partially self-supporting, and in some instances may be essentially self- supporting. The porous nonselective mechanical support layer may provide essentially all of the structural support for the membrane. Some preferred polymers different from the new polyimide polymer with a plurality of repeating units of formula (I) that are suitable for the preparation of the porous nonselective mechanical support layer for the TFC high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane according to the present invention include, but are not limited to, polysulfones, sulfonated polysulfones, polyethersulfones (PESs), sulfonated PESs, polyethers, polyetherimides such as Ultem, cellulosic polymers such as cellulose acetate and cellulose triacetate, polyamides, polyimides such as P84 and P84HT, polyether ketones, and blends thereof.
[0034] The present invention provides another method for the preparation of high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross- linked polyimide thin film composite hollow fiber membrane including: 1) preparing a spinning sheath dope solution of the new polyimide polymer with a plurality of repeating units of formula (I) by: a) dissolving 3-isocyanatopropyltrialkyloxysilane such as 3- isocyanatopropyltriethoxysilane and a polyimide polymer with a plurality of repeating units of formula (II) in an organic solvent such as N-methyl 2-pyrrolidone ( MP), 1,3-dioxolane, tetrahydrofuran (THF), and cyclohexanone to form a homogeneous solution; b) heating said homogeneous solution for 24-72 hours at 40-70°C to form said spinning solution of the new polyimide polymer with a plurality of repeating units of formula (I) via the reaction between 3-isocyanatopropyltrialkyloxysilane and polyimide polymer with a plurality of repeating units of formula (II); c) in some cases, some organic solvents such as hexane, n-octane, and n-decane that cannot dissolve the new polyimide polymer with a plurality of repeating units of formula (I) are added to said spinning solution; 2) preparing a core dope solution of a cheap polymer such as polyethersulfone; 3) spinning said sheath dope solution of the new polyimide polymer with a plurality of repeating units of formula (I) and said core dope solution simultaneously in the presence of a bore fluid such as a mixture of NMP and water using a triple-annulus spinneret to form a nascent TFC hollow fiber membrane with a thin sheath layer of said sheath dope solution of the new polyimide polymer with a plurality of repeating units of formula (I); 4) removing the organic solvents from the nascent TFC hollow fiber membrane; 5) drying the membrane to form said TFC hollow fiber membrane comprising the new polyimide polymer with a plurality of repeating units of formula (I) wherein the trialkyloxysilane groups have reacted with each other and have formed covalent bonds among the polymer chains; 6) coating said dried TFC hollow fiber membrane with a thin layer of high permeability material such as a fluoropolymer or a UV radiation curable epoxy silicone; and 7) UV cross-linking said coated and dried TFC hollow fiber membrane via UV radiation to cross-link the membrane via covalent bonds between the UV cross- linkable sulfonyl or carbonyl group and methyl group on said new polyimide polymer chains with a plurality of repeating units of formula (I) to form said high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide thin film composite hollow fiber membrane.
[0035] The invention provides a process for separating at least one gas from a mixture of gases using the high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane described in the present invention, the process comprising: (a) providing a both chemically and UV cross-linked polyimide membrane described in the present invention which is permeable to said at least one gas; (b) contacting the mixture on one side of the both chemically and UV cross-linked polyimide membrane described in the present invention to cause said at least one gas to permeate the membrane; and (c) removing from the opposite side of the membrane a permeate gas composition comprising a portion of said at least one gas which permeated said membrane.
[0036] The high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane described in the present invention is especially useful in the purification, separation or adsorption of a particular species in the liquid or gas phase. In addition to separation of pairs of gases, the high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane described in the present invention may, for example, be used for the desalination of water by reverse osmosis or for the separation of proteins or other thermally unstable compounds, e.g. in the pharmaceutical and biotechnology industries. The high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane described in the present invention may also be used in fermenters and bioreactors to transport gases into the reaction vessel and transfer cell culture medium out of the vessel. Additionally, the high selectivity, high plasticization-resistant and solvent- resistant, both chemically and UV cross-linked polyimide membrane described in the present invention may be used for the removal of microorganisms from air or water streams, water purification, ethanol production in a continuous fermentation/membrane pervaporation system, and in detection or removal of trace compounds or metal salts in air or water streams.
[0037] The high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane described in the present invention is especially useful in gas separation processes in air purification, petrochemical, refinery, and natural gas industries. Examples of such separations include separation of volatile organic compounds (such as toluene, xylene, and acetone) from an atmospheric gas, such as nitrogen or oxygen and nitrogen recovery from air. Further examples of such separations are for the separation of He, CO2 or H2S from natural gas, ¾ from N2, CH4, and Ar in ammonia purge gas streams, ¾ recovery in refineries, olefin/paraffin separations such as propylene/propane separation, xylene separations, iso/normal paraffin separations, liquid natural gas separations, C2+ hydrocarbon recovery. Any given pair or group of gases that differ in molecular size, for example nitrogen and oxygen, carbon dioxide and methane, hydrogen and methane or carbon monoxide, helium and methane, can be separated using the high selectivity, high
plasticizati on-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane described in the present invention. More than two gases can be removed from a third gas. For example, some of the gas components which can be selectively removed from a raw natural gas using the high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane described herein include carbon dioxide, oxygen, nitrogen, water vapor, hydrogen sulfide, helium, and other trace gases. Some of the gas components that can be selectively retained include hydrocarbon gases. When permeable components are acid components selected from the group consisting of carbon dioxide, hydrogen sulfide, and mixtures thereof and are removed from a hydrocarbon mixture such as natural gas, one module, or at least two in parallel service, or a series of modules may be utilized to remove the acid components. For example, when one module is utilized, the pressure of the feed gas may vary from 275 kPa to 2.6 MPa (25 to 4000 psi). The differential pressure across the membrane can be as low as 70 kPa or as high as 14.5 MPa (10 psi or as high as 2100 psi) depending on many factors such as the particular membrane used, the flow rate of the inlet stream and the availability of a compressor to compress the permeate stream if such compression is desired. Differential pressure greater than 14.5 MPa (2100 psi) may rupture the membrane. A differential pressure of at least 0.7 MPa (100 psi) is preferred since lower differential pressures may require more modules, more time and compression of intermediate product streams. The operating temperature of the process may vary depending upon the temperature of the feed stream and upon ambient temperature conditions.
Preferably, the effective operating temperature of the membranes of the present invention will range from 50° to 150°C. More preferably, the effective operating temperature of the high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane of the present invention will range from 20° to 100°C, and most preferably, the effective operating temperature of the membranes of the present invention will range from 25° to 100°C.
[0038] The high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane described in the present invention are also especially useful in gas/vapor separation processes in chemical, petrochemical, pharmaceutical and allied industries for removing organic vapors from gas streams, e.g. in off-gas treatment for recovery of volatile organic compounds to meet clean air regulations, or within process streams in production plants so that valuable compounds (e.g., vinylchloride monomer, propylene) may be recovered. Further examples of gas/vapor separation processes in which the high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane described in the present invention may be used are hydrocarbon vapor separation from hydrogen in oil and gas refineries, for hydrocarbon dew pointing of natural gas (i.e. to decrease the hydrocarbon dew point to below the lowest possible export pipeline temperature so that liquid hydrocarbons do not separate in the pipeline), for control of methane number in fuel gas for gas engines and gas turbines, and for gasoline recovery. The high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane described in the present invention may incorporate a species that adsorbs strongly to certain gases (e.g. cobalt porphyrins or phthalocyanines for O2 or silver (I) for ethane) to facilitate their transport across the membrane.
[0039] The high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane described in the present invention also has immediate application to concentrate olefin in a paraffin/olefin stream for olefin cracking application. For example, the high selectivity, high plasticization-resistant and solvent- resistant, both chemically and UV cross-linked polyimide membrane described in the present invention can be used for propylene/propane separation to increase the concentration of the effluent in a catalytic dehydrogenation reaction for the production of propylene from propane and isobutylene from isobutane. Therefore, the number of stages of a propylene/propane splitter that is required to get polymer grade propylene can be reduced. Another application for the high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane described in the present invention is for separating isoparaffin and normal paraffin in light paraffin isomerization and MaxEne™, a process for enhancing the concentration of normal paraffin (n-paraffin) in the naphtha cracker feedstock, which can be then converted to ethylene. [0040] The high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane described in the present invention can also be operated at high temperature to provide the sufficient dew point margin for natural gas upgrading (e.g, CO2 removal from natural gas). The high selectivity, high plasticization- resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane described in the present invention can be used in either a single stage membrane or as the first or/and second stage membrane in a two stage membrane system for natural gas upgrading.
[0041] The high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane described in the present invention may also be used in the separation of liquid mixtures by pervaporation, such as in the removal of organic compounds (e. g., alcohols, phenols, chlorinated hydrocarbons, pyridines, ketones) from water such as aqueous effluents or process fluids. A membrane which is ethanol- selective would be used to increase the ethanol concentration in relatively dilute ethanol solutions (5-10% ethanol) obtained by fermentation processes. Another liquid phase separation example using the high selectivity, high plasticization-resistant and solvent- resistant, both chemically and UV cross-linked polyimide membrane described in the present invention is the deep desulfurization of gasoline and diesel fuels by a pervaporation membrane process similar to the process described in US 7,048,846, incorporated by reference herein in its entirety. The high selectivity, high plasticization-resistant and solvent- resistant, both chemically and UV cross-linked polyimide membrane described in the present invention that are selective to sulfur-containing molecules would be used to selectively remove sulfur-containing molecules from fluid catalytic cracking (FCC) and other naphtha hydrocarbon streams. Further liquid phase examples include the separation of one organic component from another organic component, e.g. to separate isomers of organic compounds. Mixtures of organic compounds which may be separated using the high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane described in the present invention include: ethylacetate-ethanol, diethylether- ethanol, acetic acid-ethanol, benzene-ethanol, chloroform-ethanol, chloroform-methanol, acetone-isopropylether, allylalcohol-allylether, allylalcohol-cyclohexane, butanol- butylacetate, butanol-1 -butyl ether, ethanol -ethylbutyl ether, propylacetate-propanol, isopropylether-isopropanol, methanol-ethanol-isopropanol, and ethylacetate-ethanol-acetic acid.
EXAMPLES
[0042] The following examples are provided to illustrate one or more preferred embodiments of the invention, but are not limited embodiments thereof. Numerous variations can be made to the following examples that lie within the scope of the invention.
EXAMPLE 1
Preparation of chemically cross-linked DSD A-TMPDA-HAB-ICPTESi polyimide dense film membrane and both chemically and UV cross-linked DSDA-TMPDA-HAB-ICPTESi polyimide dense film membrane
[0043] 7.0 g of poly(DSDA-TMPDA-HAB) polyimide synthesized from
polycondensation reaction of 3,3',4,4'-diphenylsulfone tetracarboxylic dianhydride (DSDA) with a mixture of 2,4,6-trimethyl-m-phenylenediamine (TMPDA) and 3,3'-dihydroxy-4,4'- diamino-biphenyl (HAB) (TMPDA/HAB=2: 1 molar ratio) was dissolved in 30.0 g of anhydrous NMP solvent. The mixture was mechanically stirred for 2 hours to form a homogeneous solution. 0.74 g of 3-isocyanatopropyltriethoxysilane (ICPTESi) was added to the poly (DSDA-TMPDA-HAB) polyimide solution. The solution was mechanically stirred for 4 hours at 65°C to allow the hydroxyl groups on poly (DSDA-TMPDA-HAB) polymer chain to react with the isocyanate groups on ICPTESi to form covalent bonds. The resulting homogeneous casting dope was allowed to degas overnight. The chemically cross-linked DSDA-TMPDA-HAB-ICPTESi polyimide dense film membrane was prepared from the bubble free casting dope on a clean glass plate using a doctor knife with an 18-mil gap. The dense film membrane together with the glass plate was heated at 60°C for 12 hours on top of a hot plate. The solvents were removed slowly, The dense film membrane was then heated at 200°C under vacuum for 48 hours to completely remove the residual solvent. The chemically cross-linked DSDA-TMPDA-HAB-ICPTESi polyimide dense film membrane was then further UV cross-linked under UV radiation for 25 minutes to form the both chemically and UV cross-linked DSDA-TMPDA-HAB-ICPTESi polyimide dense film membrane. EXAMPLE 2
Evaluation of CO 2 /CH 4 , H 2 /CH 4 , and He/CH 4 separation performance of chemically cross-linked DSDA-TMPDA-HAB-ICPTESi and both chemically and UV
cross-linked DSDA-TMPDA-HAB-ICPTESi dense film membranes
[0044] The chemically cross-linked DSDA-TMPDA-HAB-ICPTESi and both chemically and UV cross-linked DSDA-TMPDA-HAB-ICPTESi dense film membranes were tested for CO 2 /CH 4 , H 2 /CH 4 , and He/CH 4 separations at 50°C under 791 kPa (100 psig) single feed gas pressure for CO 2 , H 2 , CH 4 , and He gases. The results are shown in Table 1. It can be seen from Table 1 that the both chemically and UV cross-linked DSDA-TMPDA-HAB-ICPTESi dense film membrane showed very high selectivities for CO 2 /CH 4 , H 2 /CH 4 , and He/CH 4 separations and the selectivities are much higher than the only chemically cross-linked DSDA-TMPDA-HAB-ICPTESi dense film membrane.
TABLE 1
CO 2 /CH 4 , H 2 /CH 4 , and He/CH 4 separation performance of chemically cross-linked DSDA-TMPDA-HAB-ICPTESi and both chemically and UV cross-linked
DSDA-TMPDA-HAB-ICPTESi dense film membranes
1 Barrer= 10 "10 cm 3 (STP).cm/cm 2 s (cm Hg)
Testing conditions: 50°C, 791 kPa (100 psig) single feed gases. EXAMPLE 3
Evaluation of C0 2 plasticization resistance of both chemically and UV cross-linked DSDA-TMPDA-HAB-ICPTESi dense film membrane
[0045] To study the effect of both chemical and UV cross-linking on the plasticization resistance of DSDA-TMPDA-HAB-ICPTESi dense film membrane, the both chemically and UV cross-linked DSDA-TMPDA-HAB-ICPTESi dense film membrane was conditioned with C0 2 at different pressures. The change of C0 2 relative permeability with the increase of the applied C0 2 pressure at 50°C was studied. It can be seen from Table 2 that no C0 2 plasticization was observed up to 4928 kPa (700 psig) pure C0 2 pressure for the both chemically and UV cross-linked DSDA-TMPDA-HAB-ICPTESi dense film membrane. The high C0 2 plasticization resistance of the both chemically and UV cross-linked DSDA- TMPDA-HAB-ICPTESi dense film membrane is mainly attributed to the chemical and UV cross-linking and formation of rigid covalently interpolymer-chain-connected cross-linked networks.
TABLE 2
Study on C0 2 plasticization resistance of both chemically and UV cross-linked DSDA-TMPDA-HAB-ICPTESi dense film membrane
Pco2, P Pco2, loopsig is the ratio of the C0 2 permeability at p C0 2 pressure to the C0 2 permeability at 100 psig C0 2 pressure;
Testing conditions: 50°C, single C0 2 feed gas. EXAMPLE 4
Preparation of chemically and UV cross-linked
TFC DSDA-TMPDA-HAB-ICPTESi polyimide hollow fiber membrane
[0046] The chemically and UV cross-linked TFC DSDA-TMPDA-HAB-ICPTESi polyimide hollow fiber membrane comprising a chemically and UV cross-linked TFC
DSDA-TMPDA-HAB-ICPTESi polyimide sheath layer is fabricated via a co-extrusion phase inversion spinning process from a sheath dope and a core dope using a triple-orifice spinneret. The core dope comprises polyethersulfone (PES) polymer, P84 polyimide, MP, L1NO 3 and lactic acid was prepared. The sheath dope comprises poly (DSDA-TMPDA-HAB) polyimide, ICPTESi, NMP, 1,3-dioxolane, isopropanol, and methylethylketone was also prepared. The core dope and sheath dope were co-extruded through a triple-orifice spinneret at 50°C. A bore fluid containing 20% by weight of water in NMP was injected to the bore of the fiber simultaneously with the co-extruding of the core dope and sheath dope. The ratio of the core dope flow rate, the sheath dope flow rate, and the bore fluid flow rate was 10: 1 : 2.7. The nascent fiber traveled through an air gap length of 13 cm at room temperature, and then was immersed into a water coagulant bath at 0°C and wound up at a rate of 23 m/min. The water-wet fiber was annealed in a hot water bath at 85°C for 30 minutes. The annealed water- wet fiber was then sequentially exchanged with methanol and hexane for three times and for 30 minutes each time, followed by drying at 85°C in an oven for 1 hour to form dried TFC hollow fiber membrane. The dried chemically cross-linked DSDA-TMPDA-HAB-ICPTESi TFC hollow fiber membrane was coated with a thin layer of an UV curable epoxysilicone SilForce* UV9315 purchased from Momentive in the presence of a
bis(dodecylphenyl)iodonium salt photocatalyst SilForce* UV9380C purchased from
Momentive. Both the UV9315 coating layer and the chemically cross-linked DSDA- TMPDA-HAB-ICPTESi polyimide sheath layer were UV cross-linked under UV radiation for 3 minutes to form the high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked DSDA-TMPDA-HAB-ICPTESi TFC hollow fiber membrane.
[0047] SPECIFIC EMBODIMENTS
While the following is described in conjunction with specific embodiments, it will be understood that this description is intended to illustrate and not limit the scope of the preceding description and the appended claims.
A first embodiment of the invention is a process for polyimide polymer comprising a plurality of repeating units of formula (I)
wherein Xi is selecte
and mixtures thereof;
and mixtures thereof; Yi is selected from the group consisting of
and mixtures thereof; Y2 is selected from the group consisting of
and mixtures thereof, and -Ri is selected from the group consisting
-H, -COCH 3 , \
/ C¾0
HN
\
CH 2
CH 2
(R 2 0) 3 Si and mixtures thereof, and -R2 is selected from the group consisting
-CH3, -C2H5 and -R3 is selected from the group consisting of
and mixtures thereof; n and m are independent integers from 2 to 500; the molar ratio of n/m is in a range of 110 to 101. An embodiment of the invention is one, any or all of prior embodiments in this paragraph u through the first embodiment in this paragraph wherein Xi
and X2 are the same and are
An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the first embodiment in this paragraph wherein Y\ is
An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the first embodiment in this paragraph wherein Y2 is
and -Ri is selected from the group consisting of .
A second embodiment of the invention is a process for polyimide polymer membrane comprising the polyimide polymer of claim 1. An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the second embodiment in this paragraph is chemically and UV cross-linked. An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the second embodiment in this paragraph comprising a thin nonporous selective separation layer formed from the polyimide polymer with a plurality of repeating units of formula (I) and a porous nonselective mechanical support layer made from a material different from the polyimide polymer with a plurality of repeating units of formula (I). An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the second embodiment in this paragraph wherein the thin nonporous selective separation layer formed from the polyimide polymer with a plurality of repeating units of formula (I) is chemically and UV cross-linked. An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the second embodiment in this paragraph wherein the material different from the polyimide polymer with a plurality of repeating units of formula (I) is selected from the group consisting of polysulfones, sulfonated polysulfones, polyethersulfones (PESs), sulfonated PESs, polyethers, polyetherimides, cellulosic polymers, polyamides, polyimides, polyether ketones, and blends thereof. A third embodiment of the invention is a process for making a chemically and UV cross-linked polyimide membrane comprising 1) preparing a casting solution of a polyimide polymer with a plurality of repeating units of a formula (I) wherein Xi is selected from the group consisting of
and mixtures thereof; wherein X2 is selected from the group consisting of
and mixtures thereof; Yi is selected from the group consisting
and mixtures thereof; Y2 is selected from the group consisting of
and mixtures thereof, and -Ri is selected from the group consisting of
and mixtures thereof, and -R2 is selected from the group consisting
-CH3, -C2H5 and -R3 is selected from the group consisting of
and mixtures thereof; n and m are independent integers from 2 to 500; the molar ratio of n/m is in a range of 110 to 101 by a) dissolving 3-isocyanatopropyltrialkyloxysilane and a polyimide polymer with a plurality of repeating units of formula (II)
wherein Xi is selected from the group consisting of
and mixtures thereof; wherein X2 is selected from the group consisting of
and mixtures thereof; Yi is selected from the group consisting of
and mixtures thereof; Y3 is selected from the group consisting of
and mixtures thereof, and -R4 is selected from the group consisting of -H, -COCH3, and mixtures thereof, and -R5 is selected from the group consisting of
anc j mixtures thereof; n and m are independent integers from 2 to 500; the molar ratio of n/m is in a range of 110 to 10 in an organic solvent to form a homogeneous solution; b) heating the homogeneous solution for 4- 8 hours at 40-70oC to form the solution of the polyimide polymer via a reaction between 3- isocyanatopropyltrialkyloxysilane and the polyimide polymer with a plurality of repeating units of formula (II); 2) casting the casting solution of the polyimide polymer with a plurality of repeating units of formula (I) on a membrane substrate or on a polymeric cloth substrate or on a clean glass plate to form a thin layer of the casting solution of the polyimide polymer with a plurality of repeating units of formula (I); 3) removing the organic solvents from the thin layer of the casting solution of the polyimide polymer to form a flat sheet membrane; 4) drying the membrane to form chemically cross-linked polyimide membrane comprising the polyimide polymer with a plurality of repeating units of formula (I) wherein the
trialkyloxysilane groups have reacted with each other and have formed covalent bonds among the polymer chains; 5) coating the dried membrane with a thin layer of high permeability material; and 6) UV cross-linking the coated and dried membrane via UV radiation to crosslink the membrane via covalent bonds between the UV cross-linkable sulfonyl or carbonyl group and methyl group on the new polyimide polymer chains with a plurality of repeating units of formula (I). An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the third embodiment in this paragraph wherein the organic solvent is selected from the group consisting of N-methyl-2-pyrrolidone, 1,3-dioxolane, tetrahydrofuran, and cyclohexanone. An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the third embodiment in this paragraph wherein an organic solvents that cannot dissolve the new polyimide polymer with a plurality of repeating units of formula (I) is added to the casting solution.
A fourth embodiment of the invention is a process for separating at least one gas from a mixture of gases using a high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane the process comprising (a) providing a both chemically and UV cross-linked polyimide membrane prepared from a polyimide polymer with a plurality of repeating units of a formula (I)
wherein Xi is selected from the group consisting of
and mixtures hereof; wherein X2 is selected from the group consisting
and mixtures thereof; Y\ is selected from the group consisting of
and mixtures thereof; Y2 is selected from the group consisting of
and mixtures thereof, and -Ri is selected from the group consisting of
-H, -COCH 3> \
o
HN
n 2 cr CH-,
(R 2 0) 3 Si^ CH2
and mixtures thereof, and -R2 is selected from the group consisting
-CH3, -C2H5
and -R3 is selected from the group consisting of
CF 3 CH 3 O
II
C C -s- o ■ s-
II
CF 3 CH 3 o
and mixtures thereof; n and m are independent integers from 2 to 500; the molar ratio of n/m is in a range of 110 to 101 wherein the polyimide membrane is permeable to the at least one gas; (b) contacting the mixture on one side of the polyimide membrane to cause the at least one gas to permeate the membrane; and (c) removing from the opposite side of the membrane a permeate gas composition comprising a portion of the at least one gas which permeated the membrane. An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the fourth embodiment in this paragraph wherein the gases comprise volatile organic compounds in air. An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the fourth embodiment in this paragraph wherein the gases comprise a mixture of helium, carbon dioxide or hydrogen sulfide in natural gas. An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the fourth embodiment in this paragraph wherein the gases comprise hydrogen in a mixture of hydrocarbon gases from a refinery. An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the fourth embodiment in this paragraph wherein the gases comprise a mixture of olefins and paraffins.
A fifth embodiment of the invention is a process for separating a liquid mixture comprising sending the liquid mixture to a high selectivity, high plasticization-resistant and solvent-resistant, both chemically and UV cross-linked polyimide membrane wherein the both chemically and UV cross-linked polyimide membrane is prepared from a polyimide polymer with a pluralit of repeating units of a formula (I)
wherein Xi is selected from the group consisting of
and mixtures thereof; wherein X2 is selected from the group consisting
and mixtures thereof; Yi is selected from the group consisting of
and mixtures thereof; Y2 is selected from the group consisting of
and mixtures thereof, and -Ri is selected from the group consisting of
-H, -COCH 3 , \
HN
-CH 2
H 7 C
■CH 2
(R 2 0) 3 Si and mixtures thereof, and -R2 is selected from the group consisting of
-CH 3 , -C2H5
and -R3 is selected from the roup consistin of
and mixtures thereof; n and m are independent integers from 2 to 500; the molar ratio of n/m is in a range of 110 to 101 wherein the polyimide membrane is permeable to the at least one component of the liquid; (b) contacting the liquid mixture on one side of the polyimide membrane to cause the at least one liquid to permeate the membrane; and (c) removing from the opposite side of the membrane a permeate liquid composition comprising a portion of the at least one liquid which permeated the membrane. An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the fifth embodiment in this paragraph wherein the liquid mixture comprises at least one organic compound in water. An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the fifth embodiment in this paragraph wherein the organic compounds are selected from the group consisting of alcohols, phenols, chlorinated hydrocarbons, pyridines, and ketones. An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the fifth embodiment in this paragraph wherein the liquid mixture comprises a fermentation product comprising ethanol. An embodiment of the invention is one, any or all of prior embodiments in this paragraph up through the fifth embodiment in this paragraph wherein the liquid mixture comprises gasoline or diesel fuel.
Without further elaboration, it is believed that using the preceding description that one skilled in the art can utilize the present invention to its fullest extent and easily ascertain the essential characteristics of this invention, without departing from the spirit and scope thereof, to make various changes and modifications of the invention and to adapt it to various usages and conditions. The preceding preferred specific embodiments are, therefore, to be construed as merely illustrative, and not limiting the remainder of the disclosure in any way whatsoever, and that it is intended to cover various modifications and equivalent arrangements included within the scope of the appended claims.
In the foregoing, all temperatures are set forth in degrees Celsius and, all parts and percentages are by weight, unless otherwise indicated.