TRIPTYCENE-PHENANTHROLINE BASED MICROPOROUS POLYMER FOR CO2 CAPTURE OVER CH4 AND N2

Abstract

A microporous polymer material that includes reacted units of a triptycene compound and a phenanthroline compound in the form of a contorted polymeric structure. A molar ratio of the triptycene compound to the phenanthroline compound is in a range of 1:1 to 1:4. The triptycene compound is covalently bonded to the phenanthroline compound in the formation of the microporous polymer material.

Claims

1. A microporous polymer material, comprising: a polymer comprising reacted units of a triptycene compound and a phenanthroline compound, wherein the polymer has a contorted polymeric structure; wherein a molar ratio of the triptycene compound to the phenanthroline compound is in a range of 1:1 to 1:4; and wherein, in the polymer, the triptycene compound is covalently bonded to the phenanthroline compound.

2. The microporous polymer material of claim 1, wherein the triptycene compound has a formula (I): ##STR00007## wherein R.sub.1 to R.sub.12 are each independently selected from the group consisting of a hydrogen atom, a halogen atom, an optionally substituted alkyl, an optionally substituted aryl, and an optionally substituted heterocyclic aryl.

3. The microporous polymer material of claim 2, wherein the triptycene compound is 9,10-Dihydro-9,10-[1,2]benzenoanthracene.

4. The microporous polymer material of claim 1, wherein the phenanthroline compound has a formula (II): ##STR00008## wherein R.sub.13 and R.sub.20 are each independently a halogen atom; and wherein R.sub.14 to R.sub.19 are each independently selected from the group consisting of a hydrogen atom, a halogen atom, an optionally substituted alkyl, an optionally substituted aryl, and an optionally substituted heterocyclic aryl.

5. The microporous polymer material of claim 4, wherein the phenanthroline compound is 2,9-dichloro-1,10-phenanthroline.

6. The microporous polymer material of claim 1, wherein the reacted units have a formula (III): ##STR00009## wherein is an adjacent contorted polymeric structure.

7. The microporous polymer material of claim 1, wherein particles of the microporous polymer material are in the form of microspheres having an average diameter in a range of 0.5 to 1 micrometer (m).

8. The microporous polymer material of claim 7, wherein the microspheres are aggregated.

9. The microporous polymer material of claim 1, having a Brunauer-Emmett-Teller (BET) surface area of 1100 to 1200 square meter per gram (m.sup.2/g).

10. The microporous polymer material of claim 1, having a total pore volume (V.sub.tot) of 0.6 to 0.7 cubic centimeters per gram (cm.sup.3/g).

11. The microporous polymer material of claim 1, having a micropore volume (V.sub.mic) of 0.4 to 0.5 cm.sup.3/g.

12. The microporous polymer material of claim 1, having a carbon dioxide (CO.sub.2) isosteric heat of adsorption (Q.sub.st) of 20 to 30 kilojoules per mole (KJ/mol).

13. The microporous polymer material of claim 1, having a CO.sub.2 uptake of about 2.5 to 3 millimoles per gram (mmol/g) of the microporous polymer material at about 273 K and 1 bar.

14. The microporous polymer material of claim 1, having a CO.sub.2 uptake of about 1.5 to 2.3 mmol/g at about 298 K and 1 bar.

15. The microporous polymer material of claim 1, having a thermal degradation temperature of 350 to 420 C., wherein the thermal degradation temperature is determined at a weight loss of 10 percent by weight based on an initial weight of the microporous polymer material.

16. A method for capturing carbon dioxide directly from a CO.sub.2-containing gaseous composition, comprising: contacting and passing the CO.sub.2-containing gaseous composition through particles of the microporous polymer material of claim 1, thereby adsorbing at least a portion of CO.sub.2 from the CO.sub.2-containing gaseous composition onto surfaces of the microporous polymer material particles and forming a purified gas composition.

17. The method of claim 16, wherein the CO.sub.2 is present in the CO.sub.2-containing gaseous composition in an amount of 5 to 60 vol. % based on a total volume of the CO.sub.2-containing gaseous composition.

18. The method of claim 16, wherein the CO.sub.2-containing gaseous composition comprises CO.sub.2 and N.sub.2, and wherein the microporous polymer material has a Henry's Law selectivity for CO.sub.2 over N.sub.2 of about 20 to 27.8 at 270-300 K and 1 bar.

19. The method of claim 16, wherein the CO.sub.2-containing gaseous composition comprises CO.sub.2 and CH.sub.4, and wherein the microporous polymer material has a Henry's Law selectivity for CO.sub.2 over CH.sub.4 of about 3.8 to 5.8 at 270-300 K and 1 bar.

20. The method of claim 16, further comprising: preparing the microporous polymer material by: mixing a triptycene compound, a phenanthroline compound, and an aluminum salt in an organic solvent to form a mixture; wherein a molar ratio of the triptycene compound to the phenanthroline compound is in a range of 1:1 to 1:2; wherein a molar ratio of the triptycene compound to the aluminum salt is in a range of 1:2 to 1:8; heating and refluxing the mixture to form the microporous polymer material in the mixture; and separating the microporous polymer material from the mixture by filtering, washing, and drying.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0029] A more complete appreciation of this disclosure and many of the attendant advantages thereof may be readily obtained as the same becomes better understood by reference to the following detailed description when considered in connection with the accompanying drawings, wherein:

[0030] FIG. 1A is a flow chart depicting a method for preparing the microporous polymer material, according to certain embodiments.

[0031] FIG. 1B is a schematic representation for the synthesis of 3D-triptycene and phenanthroline-based microporous polymer (TPPM), according to certain embodiments.

[0032] FIG. 2A shows a Fourier-transform infrared (FTIR) spectra of the TPPM, according to certain embodiments.

[0033] FIG. 2B shows a .sup.13C Cross-Polarization Magic-Angle-Spinning Nuclear magnetic resonance (.sup.13C CP/MAS NMR) spectra of the TPPM, according to certain embodiments.

[0034] FIG. 3A shows a powder X-ray diffraction (PXRD) pattern of the TPPM, according to certain embodiments.

[0035] FIG. 3B shows a thermogravimetric analysis (TGA) analysis of the TPPM, according to certain embodiments.

[0036] FIG. 4A is a field-emission scanning electron microscopy (FE-SEM) image of the TPPM at 2 micrometers (m) magnification, according to certain embodiments.

[0037] FIG. 4B is an FE-SEM image of the TPPM at 1 m magnification, according to certain embodiments.

[0038] FIG. 4C is a zoomed-in FE-SEM image of the TPPM at 1 m magnification, according to certain embodiments.

[0039] FIG. 5A is a nitrogen (N.sub.2) sorption isotherm at 77 kelvin (K) for the TPPM, according to certain embodiments.

[0040] FIG. 5B is a pore size distribution plot for the TPPM, according to certain embodiments.

[0041] FIG. 6A shows CO.sub.2 adsorption-desorption isotherms of the TPPM at various temperatures, according to certain embodiments.

[0042] FIG. 6B shows heat of adsorption of the TPPM, according to certain embodiments.

[0043] FIG. 7A shows CO.sub.2, CH.sub.4, and N.sub.2 experimental single-component adsorption isotherms of TPPM at 273 K, according to certain embodiments.

[0044] FIG. 7B shows CO.sub.2, CH.sub.4, and N.sub.2 experimental single-component adsorption isotherms of TPPM at 298 K, according to certain embodiments.

[0045] FIG. 8A shows initial gas uptake slopes of CO.sub.2, N.sub.2 and CH.sub.4 at 273 K for TPPM, according to certain embodiments.

[0046] FIG. 8B shows initial gas uptake slopes of CO.sub.2, N.sub.2 and CH.sub.4 at 298 K for TPPM, according to certain embodiments.

[0047] FIG. 9 shows BET plot of TPPM, according to certain embodiments.

DETAILED DESCRIPTION

[0048] In the drawings, reference numerals designate identical or corresponding parts throughout the several views. Further, as used herein, the words a, an, and the like generally carry a meaning of one or more, unless stated otherwise.

[0049] Furthermore, the terms approximately, approximate, about, and similar terms generally refer to ranges that include the identified value within a margin of 20%, 10%, or preferably 5%, and any values therebetween.

[0050] As used herein, the words a and an and the like carry the meaning of one or more. Within the description of this disclosure, where a numerical limit or range is stated, the endpoints are included unless stated otherwise. Also, all values and subranges within a numerical limit or range are specifically included as if explicitly written out.

[0051] As used herein, the term substituted refers to at least one hydrogen atom that is replaced with a non-hydrogen group, provided that normal valencies are maintained and that the substitution results in a stable compound. When a group is noted as optionally substituted, the group may or may not contain non-hydrogen substituents. When present, the substituent(s) may be selected from alkyl, halo (e.g., chloro, bromo, iodo, fluoro), hydroxyl, alkoxy, oxo, alkanoyl, aryloxy, alkanoyloxy, amino (NH.sub.2), alkylamino (NHalkyl), cycloalkylamino (NHcycloalkyl), arylamino (NHaryl), arylalkylamino (NHarylalkyl), disubstituted amino (e.g., in which the two amino substituents are selected from alkyl, aryl or arylalkyl, including substituted variants thereof, with specific mention being made to dimethylamino), alkanoylamino, aroylamino, arylalkanoylamino, thiol, alkylthio, arylthio, arylalkylthio, alkylthiono, arylthiono, arylalkylthiono, alkylsulfonyl, arylsulfonyl, arylalkylsulfonyl, sulfonamide (e.g., SO.sub.2NH.sub.2), substituted sulfonamide (e.g., SO.sub.2NHalkyl, SO.sub.2NHaryl, SO.sub.2NHarylalkyl, or cases where there are two substituents on one nitrogen selected from alkyl, aryl, or alkylalkyl), nitro, cyano, carboxy, unsubstituted amide (i.e. CONH.sub.2), substituted amide (e.g., CONHalkyl, CONHaryl, CONHarylalkyl or cases where there are two substituents on one nitrogen selected from alkyl, aryl, or alkylalkyl), alkoxycarbonyl, aryl, guanidine, heterocyclyl (e.g., pyridyl, furyl, morpholinyl, pyrrolidinyl, piperazinyl, indolyl, imidazolyl, thienyl, thiazolyl, pyrrolidyl, pyrimidyl, piperidinyl, homopiperazinyl), and mixtures thereof. The substituents may themselves be optionally substituted and may be either unprotected, or protected as necessary, as known to those skilled in the art.

[0052] As used herein, the term alkyl unless otherwise specified refers to both branched and straight chain aliphatic (non-aromatic) hydrocarbons which may be primary, secondary, and/or tertiary hydrocarbons typically having 1 to 32 carbon atoms (e.g., C.sub.1, C.sub.2, C.sub.3, C.sub.4, C.sub.5, C.sub.6, C.sub.7, C.sub.8, C.sub.9, C.sub.10, C.sub.11, C.sub.12, C.sub.13, C.sub.14, etc.) and specifically includes, but is not limited to, saturated alkyl groups such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, t-butyl, pentyl, isopentyl, neopentyl, hexyl, isohexyl, 3-methylpentyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 2-ethylhexyl, heptyl, octyl, nonyl, 3,7-dimethyloctyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, eicosyl, guerbet-type alkyl groups (e.g., 2-methylpentyl, 2-ethylhexyl, 2-proylheptyl, 2-butyloctyl, 2-pentylnonyl, 2-hexyldecyl, 2-heptylundecyl, 2-octyldodecyl, 2-nonyltridecyl, 2-decyltetradecyl, and 2-undecylpentadecyl), as well as unsaturated alkenyl and alkynyl variants such as vinyl, allyl, 1-propenyl, 2-propenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-hexenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, oleyl, linoleyl, and the like.

[0053] As used herein, the term porosity refers to a measure of the void or vacant spaces within a material.

[0054] As used herein, the term pore size may be thought of as the lengths or longest dimensions of a particle and of a pore opening.

[0055] A weight percent of a component, unless specifically stated to the contrary, is based on the total weight of the formulation or composition in which the component is included. For example, if a particular element or component in a composition or article is said to have 5 wt. %, it is understood that this percentage is in relation to a total compositional percentage of 100%.

[0056] The present disclosure is intended to include all hydration states of a given compound or formula, unless otherwise noted or when heating a material.

[0057] The present disclosure is intended to include all isotopes of a given compound or formula, unless otherwise noted.

[0058] As used herein, the term optionally substituted alkyl refers to the alkyl group which is substituted with one, two, or three substituents independently selected from hydroxyl, alkoxy, carboxy, cyano, alkoxycarbonyl, alkylthio, alkylsulfonyl, halo, haloalkoxy, CONRR or NRR (where each R is hydrogen, alkyl, hydroxyalkyl, or alkoxyalkyl, and each R is hydrogen, alkyl) or heterocyclic (preferably heterocycloamino) optionally substituted with one or two groups independently selected from alkyl, hydroxyl, alkoxy, alkylsulfonyl, halo, or CONRR where R and R are as defined above.

[0059] Aspects of the present disclosure are directed towards a novel 3D-triptycene and phenanthroline-based polymer (TPPM) that forms a porous material. The polymer has microporosity in the form of its cyclical structure. Polar functional groups are used in a simple approach for efficient carbon dioxide capture. The polymeric framework of TPPM is incorporated with 3D triptycene and phenanthroline as robust motifs to yield preferably inflexible, twisted polymeric frameworks with an abundance of micropores and ultra-micropores-conferring higher surface area, abundant microporosity, and physiochemical and thermal stability.

[0060] The present disclosure describes the synthesis, characterization, and CO.sub.2 capture studies of the novel TPPM. The polymeric framework of TPPM is incorporated with 3D triptycene and phenanthroline as robust motifs to yield inflexible, twisted polymeric frameworks with an abundance of micropores and ultra-micropores. This confers desirable features such as higher surface area, abundance microporosity, and physiochemical and thermal stability. TPPM demonstrated excellent thermal stability (T.sub.d>380 C.) with a larger Brunauer-Emmett-Teller (BET)-specific surface area of 1120 square meters per gram (m.sup.2g.sup.1), and considerable microporosity which makes it a promising adsorbent for CO.sub.2 capture applications. The morphological characterization of the polymer sample shows the formation of microspheres with diameters around 0.5 to 1 micrometer (m). TPPM has a strong affinity for CO.sub.2 with Q.sub.st of 23 kilojoules per mole (KJ mol.sup.1) demonstrating promising CO.sub.2 capture capacity of 2.76 millimoles per gram (mmol g.sup.1) at 273 K and 1.85 mmol g.sup.1 at 298 K where the micropore volume (V.sub.mic=0.445 centimeters per gram (cm.sup.3 g.sup.1)) plays a potential role. TPPM also demonstrated promising CO.sub.2 selectivity over CH.sub.4 and N.sub.2, showing good promise for CO.sub.2 adsorption and separation.

[0061] In an exemplary embodiment, a microporous polymer and corresponding polymer material is described. The microporous polymer and polymer material include reacted units of a triptycene compound and a phenanthroline compound in the form of a contorted polymeric structure. Triptycene is a unique molecular unit with three blades, each composed of a benzene ring. Its rigid, three-dimensional framework makes it an intriguing building block for various applications. Triptycene is a distinctive three-dimensional molecule having three arene rings oriented in a paddle wheel fashion. Internal free volume (IFV) and excellent thermal stability are known characteristics of its unique rigid and sturdy structure.

[0062] In some embodiments, the triptycene compound has a formula (I):

##STR00004##

[0063] R.sub.1 to R.sub.12 are each independently selected from the group consisting of a hydrogen atom, a halogen atom, an optionally substituted alkyl, an optionally substituted aryl, and an optionally substituted heterocyclic aryl. In some embodiments, the triptycene compound is 9,10-dihydro-9,10-[1,2]benzenoanthracene. In some embodiments, the phenanthroline compound has a formula (II):

##STR00005##

[0064] R.sub.13 and R.sub.20 are each independently a halogen atom. R.sub.14 to R.sub.19 are each independently selected from the group consisting of a hydrogen atom, a halogen atom, an optionally substituted alkyl, an optionally substituted aryl, and an optionally substituted heterocyclic aryl. In some embodiments, the phenanthroline compound is 2,9-dichloro-1,10-phenanthroline. The molar ratio of the triptycene compound to the phenanthroline compound is in a range of 1:1 to 1:4, more preferably 0.68. The triptycene compound is covalently bonded to the phenanthroline compound in the formation of the microporous polymer material.

[0065] In some embodiments, the reacted units have a formula (III):

##STR00006##

[0066] is an adjacent contorted polymeric structure.

[0067] In some embodiments, particles of the microporous polymer material are in the form of microspheres having an average diameter in a range of 0.5 to 1 micrometer (m). The particles may exist in various morphological shapes, such as rods, spheres, wires, crystals, rectangles, triangles, pentagons, hexagons, prisms, disks, cubes, ribbons, blocks, beads, toroids, discs, barrels, granules, whiskers, flakes, foils, powders, boxes, stars, tetrapods, belts, flowers, etc. and mixtures thereof. In some embodiments, the microspheres are aggregated. The polymer material and corresponding microspheres may also have micro-and/or macro-porosity.

[0068] In some embodiments, the microporous polymer TPPM is in the form of porous particles. Pores in porous particles may be micropores, mesopores, macropores, and/or a combination thereof. In a preferred embodiment, porous particles have micropores. In some embodiments, the microporous polymer material has a BET surface area of 1100 to 1200 m.sup.2/g, more preferably 1110 to 1130 m.sup.2/g, and yet more preferably 1120 m.sup.2/g. In some embodiments, the microporous polymer material has a total pore volume (V.sub.tot) of 0.6 to 0.7 cm.sup.3/g, more preferably 0.635 to 0.660 cm.sup.3/g, and yet more preferably 0.650 cm.sup.3/g. In some embodiments, the microporous polymer material has a micropore volume (V.sub.mic) of 0.4 to 0.5 cm.sup.3/g, more preferably 0.440 to 0.450 cm.sup.3/g, and yet more preferably 0.445 cm.sup.3/g. In some embodiments, the microporous polymer material has a carbon dioxide (CO.sub.2) isosteric heat of adsorption (Q.sub.st) of 20 to 30 KJ/mol, more preferably 22 to 24 KJ/mol, and yet more preferably 23 KJ/mol. In some embodiments, the microporous polymer material has a CO.sub.2 uptake of about 2.5 to 3 mmol/g, more preferably 2.5 to 2.8 mmol/g, and yet more preferably mmol/g of the microporous polymer material at about 273 K and 1 bar. In some embodiments, the microporous polymer material has a CO.sub.2 uptake of about 1.5 to 2.3 mmol/g, more preferably 1.80 to 1.90 mmol/g, and yet more preferably 1.85 mmol/g at about 298 K and 1 bar. In some embodiments, the microporous polymer material has a thermal degradation temperature of 350 to 420 C., more preferably 380 to 385 C., and yet more preferably 382 C. The thermal degradation temperature is determined at a weight loss of 10 percent by weight based on the initial weight of the microporous polymer material.

[0069] In some embodiments, a method for capturing carbon dioxide directly from a CO.sub.2-containing gaseous composition is described. The method includes contacting and passing the CO.sub.2-containing gaseous composition through particles of the microporous polymer material, thereby adsorbing at least a portion of CO.sub.2 from the CO.sub.2-containing gaseous composition onto surfaces and/or into the pores of the microporous polymer material particles and forming a purified gas composition. In some embodiments, the CO.sub.2 is present in the CO.sub.2-containing gaseous composition in an amount of 5 to 60 vol. % based on the total volume of the CO.sub.2-containing gaseous composition. In some embodiments, the CO.sub.2-containing gaseous composition includes CO.sub.2 and N.sub.2. The microporous polymer material has a Henry's Law selectivity for CO.sub.2 over N.sub.2 of 18 to 30 or about 20 to 27.8 at 270-300 K and 1 bar, preferably 22 to 25 or about 24. In some embodiments, the CO.sub.2-containing gaseous composition includes CO.sub.2 and CH.sub.4. The microporous polymer material has a Henry's Law selectivity for CO.sub.2 over CH.sub.4 of about 3.8 to 5.8 at 270-300 K and 1 bar.

[0070] FIG. 1A illustrates a flow chart of a method 50 for preparing the microporous polymer material. The order in which the method 50 is described is not intended to be construed as a limitation, and any number of the described method steps can be combined in any order to implement the method 50. Additionally, individual steps may be removed or skipped from the method 50 without departing from the spirit and scope of the present disclosure.

[0071] At step 52, the method 50 includes mixing a triptycene compound, a phenanthroline compound, and an aluminum salt in an organic solvent to form a mixture. In some embodiments, the aluminum salt may include aluminum chloride, aluminum nitrate, and aluminum sulphate. In a preferred embodiment, the aluminum salt is aluminum chloride. In some embodiments, the organic solvent may include tetrahydrofuran, ethyl acetate, dimethylformamide, acetonitrile, acetone, dimethyl sulfoxide, nitromethane, propylene carbonate, ethanol, formic acid, n-butanol, methanol, or any combination thereof. In some embodiments, the organic solvent may include benzene, cyclohexane, ethanol, methanol, acetone, ethyl acetate, dichloromethane, toluene, and diethyl ether. The mixing may be carried out manually or with the help of a stirrer. The molar ratio of the triptycene compound to the phenanthroline compound is in a range of 1:1 to 1:2, more preferably 0.68. The molar ratio of the triptycene compound to the aluminum salt is in a range of 1:2 to 1:8 or 1:4 to 1:6 or more preferably 0.477.

[0072] At step 54, the method 50 includes heating and refluxing the mixture to form the microporous polymer material in the mixture. The reflux can be done for 18-30 hours (h), preferably 19-29 h, preferably 20-28 h, preferably 21-27 h, preferably 22-26 h, and preferably 23-25 h, to form a solid. In a preferred embodiment, the mixture is refluxed for 24 hours, preferably with alcohol. The alcohol such as methanol, ethanol, propanol, isopropanol, butanol, pentanol, and hexanol. In a preferred embodiment, the solid is refluxed with methanol.

[0073] At step 56, the method 50 includes separating the microporous polymer material from the mixture by filtering, washing, and drying. The filtration can be done by methods used or known in the art. In a preferred embodiment, the filtration is done by glass frit. After filtration, the solid may be washed using a solvent like water, methanol, ethanol, acetone, DMSO, DMF, dimethylacetamide, isopropanol, benzene, hexane, carbon tetrachloride, toluene, diethyl ether, THF, DCM, chloroform, or a mixture thereof. In a preferred embodiment, the solid is washed using DCM, water, methanol, THF, and acetone. After washing, the solid is dried at 120 C. in a vacuum oven for 24 h. In some embodiments, the drying can be performed by using heating appliances such as ovens, microwaves, autoclaves, hot plates, heating mantles, tapes, oil baths, salt baths, sand baths, air baths, hot-tube furnaces, and hot-air guns.

[0074] The TPPM prepared by the method of present disclosure demonstrates excellent thermal stability (T.sub.d>380 C.) with a larger Brunauer-Emmett-Teller (BET)-specific surface area of 1120 square meters per gram (m.sup.2g.sup.1), and considerable microporosity which makes it a promising adsorbent for CO.sub.2 capture applications. The morphological characterization of the polymer sample shows the formation of microspheres with diameters around 0.5 to 1 micrometer (m). TPPM has a strong affinity for CO.sub.2 with Q.sub.st of 23 kilojoules per mole (KJ mol.sup.1), demonstrating promising CO.sub.2 capture capacity of 2.76 millimoles per gram (mmol g.sup.1) at 273 K and 1.85 mmol g.sup.1 at 298 K where the micropore volume (V.sub.mic=0.445 centimeters per gram (cm.sup.3 g.sup.1)) plays a potential role. TPPM also demonstrated promising CO.sub.2 selectivity over CH.sub.4 and N.sub.2, showing good promise for CO.sub.2 adsorption and separation.

EXAMPLES

[0075] The following examples demonstrate a microporous polymer material. The examples are provided solely for illustration and are not to be construed as limitations of the present disclosure, as many variations thereof are possible without departing from the spirit and scope of the present disclosure.

Example 1. Chemicals and Materials

[0076] 2,9-dichloro-1,10-phenanthroline, triptycene, and AlCl.sub.3 (anhydrous) were purchased from Sigma-Aldrich. Without additional purification, the following substances were utilized after being purchased from Sigma-Aldrich: anhydrous dichloromethane (DCM), hydrochloric acid (37%), methanol (99.6%), acetone (99.5%), dimethyl sulfoxide (DMSO), and tetrahydrofuran (THF, 99.9%).

Example 2: Synthesis of TPPM

[0077] The synthesis of TPPM was carried out as follows: A mixture of triptycene (254 mg, 1 mmol), 2,9-dichloro-1,10-phenanthroline (373.5 mg, 1.5 mmol), and AlCl.sub.3 (532 mg, 4 mmol) was taken in a 100 milliliters (ml) round bottom flask with a three-necked adapter. The flask was purged with nitrogen and then filled with dry DCM (30 mL). This reaction mixture was heated and stirred under reflux for 24 hours. After cooling, the solid polymer was filtered through a glass frit and washed sequentially with DCM, water, methanol, THF, and acetone. The polymer was purified by Soxhlet extraction using a 1:99 (v/v) solution of hydrochloric acid and methanol for 24 h. The brown-colored solid polymer was dried in a vacuum oven at 120 C. for 24 h to obtain TPPM as the desired polymer. Yield: 96%; FT-IR: 3013 (CH), 2968-2922 (CH), 1692 (CN), 1603-1458 (ArCC), 1370, 1179, 1150, 900, 807, 749 cm.sup.1.

Example 3: Structural Characterizations

[0078] The functional groups of the resultant polymer (TPPM) were characterized by Fourier-transform infrared (FTIR) spectroscopy using a Nicolet 6700 FTIR instrument (Thermo Fisher Scientific, USA). The solid-state .sup.13C CP-MAS NMR spectra of TPPM were recorded on a Bruker 400 megahertz (MHz) instrument, operating at 125.65 MHz at room temperature. The morphology of TPPM was observed by FE-SEM on a TESCAN-LYRA-3, Czech Republic) instrument with high resolution. The amorphous nature of TPPM was determined by powder XRD with a Rigaku Miniflex-II diffractometer instrument that had a Cu-K anode (=0.15416 nanometers (nm)). The thermal stability of TPPM was measured by TGA on a TA Q500 instrument under 10 ml min.sup.1 airflow with a heating rate of 10 C. min.sup.1. The N.sub.2 isotherm data acquired by a Quadrasorb SI instrument (Quantachrome Instruments, US) was used to compute the textural parameters of TPPM, including porosity, surface area, and pore volumes.

Example 4: Gas Adsorption Experiment

[0079] A Quadrasorb SI system (Quantachrome Instruments, US) was utilized to analyze the CO.sub.2, CH.sub.4, and N.sub.2 adsorption isotherms at different temperatures. Approximately 200 milligrams of the sample were pretreated for 12 h at 120 C. under a dynamic vacuum (10.sup.5 bar) before the isotherm measurements. The isotherm temperatures were maintained to within 1 C. using a flow bath filled with an equimolar combination of water and ethylene glycol.

Result and Discussion

[0080] A facile one-pot Friedel-Crafts crosslinking polymerization reaction was used to synthesize the polymer TPPM by using triptycene and 2,9-dichloro-1,10-phenanthroline as monomers (FIG. 1B). TPPM is solid with a brown color and does not dissolve in many common organic solvents, such as DCM, DMSO, DMF, and THF. The solubility test results are shown in Table 1. The .sup.13C CP/MAS NMR and FTIR spectroscopy were used for structural characterizations of TPPM. FT-IR spectrum of the polymer TPPM is shown in FIG. 2A. In the FT-IR spectrum of TPPM, the peak due to the existence of CN functionality in the polymer appeared at about 1695 cm.sup.1. Additionally, the peak observed at 2960 cm.sup.1 corresponds to the stretching vibration of triptycene bridge head CH groups indicating successful crosslinking. The different aromatics CC stretching vibrations peaks appeared in the range of 1603-1458 cm.sup.1.

TABLE-US-00001 TABLE 1 Solubility analysis of TPPM in different solvents Name of Solvents TPPM Dichloromethane (DCM) Insoluble Methanol Insoluble Tetrahydrofuran (THF) Insoluble Ethyl acetate Insoluble Dimethoxy sulfoxide (DMSO) Insoluble Dimethylacetamide (DMAc) Insoluble Dimethyl formamide (DMF) Insoluble

[0081] FIG. 2B shows the .sup.13C CP/MAS NMR spectrum of TPPM. As anticipated, the broad peaks in the range of 140-85 parts per million parts per million (ppm) correspond to the aromatic carbons of the polymeric framework. The peak at 129 ppm was assigned to imine-substituted aromatic carbon (CN). The peaks due to bridgehead carbon of triptycene (CH) motifs appeared at about 50-30 ppm. Therefore, .sup.13C CP/MAS NMR analysis clearly showed the successfully incorporated 3D-triptycene and phenanthroline units in the polymeric network of TPPM.

[0082] Powder X-ray diffraction (PXRD) analysis of TPPM is displayed in FIG. 3A. The featureless broad spectrum in the PXRD pattern shows that TPPM is amorphous in nature. This may be ascribed to the existence of robust, and bulky triptycene units in the polymeric network of TPPM. The thermal behavior of the TPPM sample was investigated by thermogravimetric analysis (TGA) under airflow, as depicted in FIG. 3B. The sample was placed in an alumina crucible and heated from room temperature to 800 C. at a heating rate of 10 C. The weight loss curve was recorded as a function of temperature.

[0083] High thermal stability was shown by TPPM, as revealed by its TGA analysis experiment (FIG. 3B). For TPPM, the thermal degradation temperature (T.sub.d) was 382 C.; at this point, only 10% weight loss was observed. The existence of stiff robust triptycene units in the polymeric network is attributed to TPPM's excellent thermal stability. The morphology of TPPM was studied further using field-emission scanning electron microscopy (FESEM). As shown in FIGS. 4A-4C, FESEM micrographs of TPPM reveal the formation of microspheres with diameters in the range of 0.5-1 micrometers (m).

[0084] The adsorption and desorption isotherms of N.sub.2 at 77 K and 1 bar pressure were conducted to analyze the textural properties of the samples, such as pore volumes, surface area, and porosity. FIG. 5A illustrates that TPPM exhibited a steep N.sub.2 adsorption at very low-pressure ratios (P/P.sub.0=0-0.01), while the isotherms gradually increased with higher pressure up to 1 bar. This indicates that while some mesopores are present, micropores include the majority of the pores in TPPM.

[0085] The N.sub.2 sorption isotherm reveals that TPPM has a significant microporosity, with most of the pores having a diameter of 0.95 nm. This is confirmed by the pore size distribution (PSD) plot derived from the DFT method (FIG. 5B). One possible explanation for TPPM's microporous nature is the presence of 3D triptycene units with internal free volumes (IFV) and the rigid concave-shaped phenanthroline producing a contorted polymeric network with microporosity. TPPM revealed a high BET-specific surface area (SA.sub.BET) of 1120 meter square per gram (m.sup.2 g.sup.1) (FIG. 9) with a total pore volume (V.sub.tot) of 0.650 cubic centimeters per gram (cm.sup.3 g.sup.1) and micropore volume (V.sub.mic) of 0.445 cm.sup.3 g.sup.1 (Table 2). The measured S.sub.ABET of TPPM is found to be greater compared to several porous polymers documented in the literature, including azo-functionalized POPs (TAPs, 474-772 m.sup.2 g.sup.1) [See: Bera, R.; Ansari, M.; Alam, A.; Das, N. Triptycene, Phenolic-OH, and Azo-Functionalized Porous Organic Polymers: Efficient and Selective CO2 Capture. ACS Appl Polym Mater 2019, 1, 959-968]. Guanidium-based porous network (iCON-5, 53.17 m.sup.2 g.sup.1) [See: Chandra, S.; Hassan, A.; Prince; Alam, A.; Das, N. Rapid and Efficient Removal of Diverse Anionic Water Contaminants Using a Guanidium-Based Ionic Covalent Organic Network (ICON). ACS Appl Polym Mater 2022, 4, 6630-6641], oxygen-rich HCPs (up to 246.9 m.sup.2 g.sup.1) [See: Shao, L.; Liu, N.; Wang, L.; Sang, Y.; Wan, H.; Zhan, P.; Zhang, L.; Huang, J.; Chen, J. Facile Preparation of Oxygen-Rich Porous Polymer Microspheres from Lignin-Derived Phenols for Selective CO.sub.2 Adsorption and Iodine Vapor Capture. Chemosphere 2022, 288, 132499], HCTIn hyper crosslinked networks (445-560 m.sup.2 g.sup.1) [See: Wen, J.; Xiao, L.; Sun, T.; Lei, Z.; Chen, H.; Li, H. Fine Tuning of Specific Surface Area and CO.sub.2 Capture Performance in Hyper-Cross-Linked Heterocyclic Networks with Tetrazinyl Linker. Microporous Mesoporous Mater. 2021, 319, 111069], phenanthroimidazole-based POPs (CPPs, 49-285 m.sup.2 g.sup.1) [See: Monterde, C.; Navarro, R.; Iglesias, M.; Snchez, F. Fluorine-Phenanthroimidazole Porous Organic Polymer: Efficient Microwave Synthesis and Photocatalytic Activity. ACS Appl Mater Interfaces 2019, 11, 3459-3465], pyrrolidinone-based HCPs (up to 584 m.sup.2 g.sup.1) [See: Li, X.; Chen, G.; Ma, J.; Jia, Q. Pyrrolidinone-Based Hypercrosslinked Polymers for Reversible Capture of Radioactive Iodine. Sep Purif Technol 2019, 210, 995-1000], heteroatoms containing POPs (HPOPs, 49-89 m.sup.2 g.sup.1) [See: Hassan, A.; Das, N. Chemically Stable and Heteroatom Containing Porous Organic Polymers for Efficient Iodine Vapor Capture and Its Storage. ACS Appl Polym Mater 2023, 5, 5349-5359], indone-based POPs (PHOIN_NH2, 509 m.sup.2 g.sup.1) [See: Xu, Y.; Wang, C.; Yang, L.; Chang, G. Sandwich-like Structure of Indole and Carbon Dioxide with Efficient CO2 Capture and Conversion. ACS Appl Polym Mater 2019, 1, 3389-3395], and triazine-based porous polymers (308-456 m.sup.2 g.sup.1) [See: Geng, T.; Zhang, W.; Zhu, Z.; Kai, X. Triazine-Based Conjugated Microporous Polymers Constructing Triphenylamine and Its Derivatives with Nitrogen as Core for lodine Adsorption and Fluorescence Sensing I2. Microporous Mesoporous Mater. 2019, 273, 163-170].

TABLE-US-00002 TABLE 2 Porous property, adsorption capacity, and value of selectivity of TPPM measured at various temperatures. CO.sub.2 CO.sub.2 Q.sub.st uptake at uptake at of Selectivity Selectivity SA.sub.BET V.sub.total V.sub.mic 273 K 298 K CO.sub.2 CO.sub.2/N.sub.2 CO.sub.2/CH.sub.4 (m.sup.2 (cm.sup.3 (cm.sup.3 and 1 bar and 1 bar (kJ 273 K 273 K Material g.sup.1) g.sup.1) g.sup.1) (mmol/g) (mmol/g) mol.sup.1) (298 K) (298 K) TPPM 1120 0.65 0.445 2.76 1.85 23 27.8 (20) 5.8 (3.8)

[0086] CO.sub.2 uptake isotherms were measured at different temperatures to assess the CO.sub.2 capture capability of TPPM, illustrated in FIG. 6A. The CO.sub.2 adsorption-desorption isotherm reveals the reversible CO.sub.2 uptake ability of TPPM as evident from its hysteresis-free isotherm nature (FIG. 6A). The CO.sub.2 adsorption capacity of TPPM at various temperatures is displayed in Table 2. TPPM can adsorb 2.76 mmol/g of CO.sub.2 at 273 K and 1.85 mmol/g of CO.sub.2 at 298 K. The CO.sub.2 adsorption performance of TPPM at 273K is superior compared to many other porous polymers that have been reported previously for CO.sub.2 adsorption, as displayed in Table 3, a comparison of TPPM's CO.sub.2 uptake performance with other porous polymers reported in the literature. Some representative examples include the capture capabilities of porous polymers based on tetraphenyl anthraquinone (An-CPOPs, 1.40-1.51 mmol/g) [See: Mohamed, M. G.; Zhang, X.; Mansoure, T. H.; El-Mahdy, A. F. M.; Huang, C.-F.; Danko, M.; Xin, Z.; Kuo, S.-W. Hypercrosslinked Porous Organic Polymers Based on Tetraphenylanthraquinone for CO.sub.2 Uptake and High-Performance Supercapacitor. Polymer, 2020, 205, 122857] nitrogen rich Porous polymer (2.22 mmol/g) [See: Cui, Y.; Du, J.; Liu, Y.; Yu, Y.; Wang, S.; Pang, H.; Liang, Z.; Yu, J. Design and Synthesis of a Multifunctional Porous N-Rich Polymer Containing s-Triazine and Trger's Base for CO2 Adsorption, Catalysis and Sensing. Polym Chem 2018, 9, 2643-2649] triphenylamine- and triphenyl triazine-based-COFs (2.09 mmol/g) [See: El-Mahdy, A. F. M.; Kuo, C. H.; Alshehri, A.; Young, C.; Yamauchi, Y.; Kim, J.; Kuo, S. W. Strategic Design of Triphenylamine- and Triphenyltriazine-Based Two-Dimensional Covalent Organic Frameworks for CO.sub.2 Uptake and Energy Storage. J Mater Chem A 2018, 6, 19532-19541] triazine based covalent imine framework (TPA-TCIF (BD), 1.75 mmol/g)] [See: Puthiaraj, P.; Kim, H. S.; Yu, K.; Ahn, W. S. Triphenylamine-Based Covalent Imine Framework for CO2 Capture and Catalytic Conversion into Cyclic Carbonates. Microporous Mesoporous Mater. 2020, 297, 110011] phthalazinone-based CTFs (PHCTFs, 1.90-2.34 mmol/g) [See: Yuan, K.; Liu, C.; Zong, L.; Yu, G.; Cheng, S.; Wang, J.; Weng, Z.; Jian, X. Promoting and Tuning Porosity of Flexible Ether-Linked Phthalazinone-Based Covalent Triazine Frameworks Utilizing Substitution Effect for Effective CO.sub.2 Capture. ACS Appl Mater Interfaces 2017, 9, 13201-13212] microporous polymer network (6FA-PI-CL, 1.65 mmol/g) [See: Song, N.; Wang, T.; Yao, H.; Ma, T.; Shi, K.; Tian, Y.; Zou, Y.; Zhu, S.; Zhang, Y.; Guan, S. Construction and Carbon Dioxide Capture of Microporous Polymer Networks with High Surface Area Based on Cross-Linkable Linear Polyimides. Polym Chem 2019, 10, 4611-4620] nitro-functionalized porous polymer (PAN-NP, 2.34 mmol/g) [See: Zhang, B.; Yan, J.; Li, G.; Wang, Z. Carboxyl-, Hydroxyl-, and Nitro-Functionalized Porous Polyaminals for Highly Selective CO2 Capture. ACS Appl Polym Mater 2019, 1, 1524-1534] and bicarbazole based porous polymers (CMPs, up to 2.12 mmol/g) [See: Yuan, Y.; Huang, H.; Chen, L.; Chen, Y. N,N-Bicarbazole: A Versatile Building Block toward the Construction of Conjugated Porous Polymers for CO.sub.2 Capture and Dyes Adsorption. Macromolecules 2017, 50, 4993-5003]. At 298 K, TPPM's CO.sub.2 adsorption capacity is 1.85 mmol/g which is also comparable to or greater than that of several other porous polymers, including POP101-104 (0.92-0.87 mmol/g) [See: Abdelnaby, M. M.; Aliyu, M.; Nemitallah, M. A.; Alloush, A. M.; Mahmoud, E. H. M.; Ossoss, K. M.; Zeama, M.; Dowaidar, M. Design and Synthesis of N-Doped Porous Carbons for the Selective Carbon Dioxide Capture under Humid Flue Gas Conditions. Polymers 2023, 15, 2475] An-CPOPs (1.29-1.40 mmol/g) [See: Mohamed, M. G.; Zhang, X.; Mansoure, T. H.; El-Mahdy, A. F. M.; Huang, C.-F.; Danko, M.; Xin, Z.; Kuo, S.-W. Hypercrosslinked Porous Organic Polymers Based on Tetraphenylanthraquinone for CO.sub.2 Uptake and High-Performance Supercapacitor. Polymer, 2020, 205, 122857], TPT-COF-6 (1.49 mmol/g) [See: El-Mahdy, A. F. M.; Kuo, C. H.; Alshehri, A.; Young, C.; Yamauchi, Y.; Kim, J.; Kuo, S. W. Strategic Design of Triphenylamine- and Triphenyltriazine-Based Two-Dimensional Covalent Organic Frameworks for CO.sub.2 Uptake and Energy Storage. J Mater Chem A 2018, 6, 19532-19541], TPA-TCIF (BD) (1.14 mmol/g) [See: Puthiaraj, P.; Kim, H. S.; Yu, K.; Ahn, W. S. Triphenylamine-Based Covalent Imine Framework for CO.sub.2 Capture and Catalytic Conversion into Cyclic Carbonates. Microporous Mesoporous Mater. 2020, 297, 110011], iCOP (1.5 mmol/g) [Gnani Peer Mohamed, S. I.; Nguyen, T.; Bavarian, M.; Nejati, S. One-Step Synthesis of an Ionic Covalent Organic Polymer for CO.sub.2 Capture. ACS Appl Polym Mater 2022, 4 8021-8025], HCP1 (0.756 mmol/g) [See: Dong, X.; Akram, A.; Comesaa-Gndara, B.; Dong, X.; Ge, Q.; Wang, K.; Sun, S.-P.; Jin, B.; Lau, C. H. Recycling Plastic Waste for Environmental Remediation in Water Purification and CO.sub.2 Capture. ACS Appl Polym Mater 2020, 2, 2586-2593] and CMPs (up to 1.24 mmol/g) [See: Yuan, Y.; Huang, H.; Chen, L.; Chen, Y. N,N-Bicarbazole: A Versatile Building Block toward the Construction of Conjugated Porous Polymers for CO.sub.2 Capture and Dyes Adsorption. Macromolecules 2017, 50, 4993-5003].

[0087] TPPM's promising CO.sub.2 uptake performance may be ascribable to the presence highly microporous network composed of 3D triptycene and phenanthroline. The mechanism of CO.sub.2 adsorption was investigated by calculating the isosteric heat of adsorption (q.sub.st) using isotherms of CO.sub.2 adsorption for TPPM (FIG. 6B). The q.sub.st values provide information about the nature of the interactions between the adsorbent (TPPM) and the adsorbate (CO.sub.2). Given that the magnitude of q.sub.st was found to be 23 KJ mol.sup.1, it indicates that TPPM adsorbed CO.sub.2 via a physisorption mechanism. The measured q.sub.st is comparable to or less than various other heteroatoms with porous organic polymers that have been described in the literature such as TF-PI-CL (28.6-30.2 KJ mol.sup.1) [See: Song, N.; Wang, T.; Yao, H.; Ma, T.; Shi, K.; Tian, Y.; Zou, Y.; Zhu, S.; Zhang, Y.; Guan, S. Construction and Carbon Dioxide Capture of Microporous Polymer Networks with High Surface Area Based on Cross-Linkable Linear Polyimides. Polym Chem 2019, 10, 4611-4620], melamine-based porous polyamides PTPAs (29.5-34.2 KJ mol.sup.1) [See. Shao, L.; Liu, M.; Sang, Y.; Huang, J. One-Pot Synthesis of Melamine-Based Porous Polyamides for CO.sub.2 Capture. Microporous Mesoporous Mater. 2019, 285. 105-111], TPA-TCIF (BD) (33.7 KJ mol.sup.1) [See: Puthiaraj, P.; Kim, H. S.; Yu, K.; Ahn, W. S. Triphenylamine-Based Covalent Imine Framework for CO.sub.2 Capture and Catalytic Conversion into Cyclic Carbonates. Microporous Mesoporous Mater. 2020, 297, 110011], nanoporous frameworks consisting 1,3,5-triazine (NOPs, 29.2-34.1 KJ mol.sup.1) [See: Xiong, S.; Fu, X.; Xiang, L.; Yu, G.; Guan, J.; Wang, Z.; Du, Y.; Xiong, X.; Pan, C. Liquid Acid-Catalysed Fabrication of Nanoporous 1,3,5-Triazine Frameworks with Efficient and Selective CO2 Uptake. Polym Chem 2014, 5, 3424-3431], imine-based porous network polymer PIN1-2 (30 KJ mol.sup.1) [See. Popp, N.; Homburg, T.; Stock, N.; Senker, J. Porous Imine-Based Networks with Protonated Imine Linkages for Carbon Dioxide Separation from Mixtures with Nitrogen and Methane. J Mater Chem A 2015, 3, 18492-18504] and HBPI-CLs (29.1-32.8 KJ mol.sup.1) [See: Popp, N.; Homburg, T.; Stock, N.; Senker, J. Porous Imine-Based Networks with Protonated Imine Linkages for Carbon Dioxide Separation from Mixtures with Nitrogen and Methane. J Mater Chem A 2015, 3, 18492-1850].

TABLE-US-00003 TABLE 3 Comparison of CO.sub.2 uptake of TPPM with other reported porous polymers CO.sub.2 CO.sub.2 uptake at uptake at Heat of CO.sub.2/N.sub.2 CO.sub.2/CH.sub.4 1 bar 1 bar adsorption Selectivity Selectivity (mmol/g) (mmol/g) (Q.sub.st) 273 K 273 K Material 273 K 298 K (kJ/mol) (298 K) (298 K) Ref. TPPM 2.76 1.85 23 27.8 (20) 5.8 (3.8) The present disclosure HCP1b 0.82 0.53 38.2 32.8 Shao, L.; Liu, N.; Wang, L.; Sang, Y.; Wan, H.; Zhan, P.; Zhang, L.; Huang, J.; Chen, J. Facile Preparation of Oxygen-Rich Porous Polymer Microspheres from Lignin- Derived Phenols for Selective CO2 Adsorption and Iodine Vapor Capture. Chemosphere 2022, 288, 132499. An- 1.39 1.29 Mohamed, M. G.; Zhang, X.; CPOP-1 Mansoure, T. H.; El-Mahdy, A. F. M.; Huang, C.- F.; Danko, M.; Xin, Z.; Kuo, S.-W. Hypercrosslinked Porous Organic Polymers Based on Tetraphenylanthraquinone for CO2 Uptake and High- Performance Supercapacitor. Polymer, 2020, 205, 122857. PAF-32 1.66 0.9 26 Jing, X.; Zou, D.; Cui, P.; Ren, H.; Zhu, G. Facile Synthesis of Cost-Effective Porous Aromatic Materials with Enhanced Carbon Dioxide Uptake. J Mater Chem A 2013, 1, 13926-13931 HCP-BA 1.92 27.4 28 (19) Luo, Y.; Zhang, S.; Ma, Y.; Wang, W.; Tan, B. Microporous Organic Polymers Synthesized by Self- Condensation of Aromatic Hydroxymethyl Monomers. Polym Chem 2013, 4, 1126-1131 HPIL-Cl- 1.79 1 45 37 Sang, Y.; Huang, J. 2 Benzimidazole-Based Hyper- Cross-Linked Poly(Ionic Liquid)s for Efficient CO2 Capture and Conversion. Chem. Engin. J. 2020, 385, 123973. HCP-B 1.46 1.26 Huang, J.; Zhu, J.; Snyder, S. A.; Morris, A. J.; Turner, S. R. Nanoporous Highly Crosslinked Polymer Networks with Covalently Bonded Amines for CO2 Capture. Polymer 2018, 154, 55-61 CB-PCP- 2.04 1.2 35 Dani, A.; Crocell, V.; 1 Magistris, C.; Santoro, V.; Yuan, J.; Bordiga, S. Click- Based Porous Cationic Polymers for Enhanced Carbon Dioxide Capture. J Mater Chem A 2017, 5 372-383 TBP-1 1.16 0.79 33.7 Bera, R.; Mondal, S.; Das, N. Nanoporous Triptycene Based Network Polyamides (TBPs) for Selective CO2 Uptake. Polymer 2017, 111, 275-284 STNP3 1.95 1.14 22 Alam, A.; Hassan, A.; Bera, R.; Das, N. Silsesquioxane- Based and Triptycene-Linked Nanoporous Polymers (STNPs) with a High Surface Area for CO2 Uptake and Efficient Dye Removal Applications. Mater Adv 2020, 1 (9), 3406-3416 HPP-3 1.38 0.68 35 Wang, D.; Yang, W.; Feng, S.; Liu, H. Constructing Hybrid Porous Polymers from Cubic Octavinylsilsequioxane and Planar Halogenated Benzene. Polym Chem 2014, 5 3634-3642

[0088] TPPM's CO.sub.2/CH.sub.4 and CO.sub.2/N.sub.2 selectivity were assessed at different temperatures after achieving its intended CO.sub.2 adsorption performance. One of the key steps in CO.sub.2 capturing from flue gases after combustion is to separate it from N.sub.2, which normally contains approximately 15% CO.sub.2 and more than 70% N.sub.2. Furthermore, as biogas and other CH.sub.4-rich gases are frequently equimolar mixtures of CO.sub.2 and CH.sub.4, it is hepful to separate CO.sub.2 from CH.sub.4. Thus, to evaluate TPPM's potential to separate CO.sub.2/CH.sub.4 mixture (50% CO.sub.2:50% CH.sub.4) from landfill gas and CO.sub.2/N.sub.2 mixture (15/85, v/v) from flue gas.

[0089] The adsorption isotherms of N.sub.2, CH.sub.4, and CO.sub.2 were evaluated at 273 and 298 K temperature and 1 bar pressure to assess the selective CO.sub.2 capture ability of TPPM, as illustrated in FIGS. 7A-7B. The results revealed that TPPM was more effective at capturing CO.sub.2 than N.sub.2 and CH.sub.4. The adsorption isotherms at 273 and 298 K exhibited that CO.sub.2 was adsorbed significantly higher than CH.sub.4 and N.sub.2. This indicates that TMPP has a higher CO.sub.2 affinity than CH.sub.4 and N.sub.2. Notably, the CO.sub.2 uptake of TPPM at 273 K temperature was about 15 times higher than the N.sub.2 uptake at 1 bar pressure. This is because of the polarity difference between CO.sub.2 and N.sub.2, which further indicates a higher selectivity and affinity exhibited by TPPM for CO.sub.2 over N.sub.2.

[0090] The CO.sub.2/N.sub.2. and CO.sub.2/CH.sub.4 selectivity values were measured by utilizing Henry Law's initial slope ratio method (FIGS. 8A-8B), which is used for predicting the values of selectivity for the mixture of gases from experimentally obtained single-component adsorption isotherms of adsorption in a given conditions. TPPM displayed promising CO.sub.2/N.sub.2 selectivity of 27.8 at 273 K and 1 bar pressure (Table 3). The observed CO.sub.2 over N.sub.2 selectivity is also superior or comparable to many other previously reported porous polymeric adsorbents, for example, (CTFs, 13-32) [See: Dey, S.; Bhunia, A.; Breitzke, H.; Groszewicz, P. B.; Buntkowsky, G.; Janiak, C. Two Linkers Are Better than One: Enhancing CO.sub.2 Capture and Separation with Porous Covalent Triazine-Based Frameworks from Mixed Nitrile Linkers. J Mater Chem A 2017, 5, 3609-3620] (TBP-OH, 27.7) [See: Ansari, M.; Das, N. Triptycene-Based Porous Photoluminescent Polymers with Dual Role: Efficient Capture of Carbon Dioxide and Sensitive Detection of Picric Acid. Mater Today Chem 2022, 23, 100723] (TBHCP-OH, 23.1) [See: Ansari, M.; Hassan, A.; Alam, A.; Das, N. A Mesoporous Polymer Bearing 3D-Triptycene, OH and Azo-Functionalities: Reversible and Efficient Capture of Carbon Dioxide and Iodine Vapor. Microporous Mesoporous Mater. 2021, 323, 111242] (HCP-0 (16.9) [See: Fu, Z.; Mohamed, I. M. A.; Li, J.; Liu, C. Novel Adsorbents Derived from Recycled Waste Polystyrene via Cross-Linking Reaction for Enhanced Adsorption Capacity and Separation Selectivity of CO 2. J Taiwan Inst Chem Eng 2019, 97, 381-388], (TBP1, 27) [See: Bera, R.; Mondal, S.; Das, N. Nanoporous Triptycene Based Network Polyamides (TBPs) for Selective CO.sub.2 Uptake. Polymer 2017, 111, 275-284] (HCP1b, 32.8) [See: Shao, L.; Liu, N.; Wang, L.; Sang, Y.; Wan, H.; Zhan, P.; Zhang, L.; Huang, J.; Chen, J. Facile Preparation of Oxygen-Rich Porous Polymer Microspheres from Lignin-Derived Phenols for Selective CO.sub.2 Adsorption and lodine Vapor Capture. Chemosphere 2022, 288, 132499], polyethylimine grafted porous polymer (TCP-PEI, 34) [See: Ravi, S.; Choi, Y.; Park, W.; Han, H. H.; Wu, S.; Xiao, R.; Bae, Y. S. Novel Triazine Carbonyl Polymer with Large Surface Area and Its Polyethylimine Functionalization for CO.sub.2 Capture. J. Ind. Eng. Chem. 2022, 108, 188-194], and porous polyamides PTPA-3 (31.6) [See: Shao, L.; Liu, M.; Sang, Y.; Huang, J. One-Pot Synthesis of Melamine-Based Porous Polyamides for CO.sub.2 Capture. Microporous Mesoporous Mater. 2019, 285. 105-111]. At 298 K, TPPM's CO.sub.2/N.sub.2 selectivity was estimated to be 20. The CO.sub.2/CH.sub.4 selectivity values were measured to be 5.8 and 3.8 at 273 and 298 K temperatures, respectively. At a given temperature the selectivity of CO.sub.2/N.sub.2 is relatively higher than that of CO.sub.2/CH.sub.4 selectivity as CO.sub.2 and N.sub.2 show a greater difference in polarizability as compared to CO.sub.2 and CH.sub.4. Further, the selectivity decreases with increasing temperature for both CO.sub.2/N.sub.2 and CO.sub.2/CH.sub.4 separation, indicating that the adsorbent shows both better capacity and selectivity at 273 K. Further, at both investigated temperatures, CO.sub.2 capacity is the highest, followed by CH.sub.4 and N.sub.2 is the least adsorbed. This is attributed to the highest polarizability (2.507 cubic angstrom (.sup.3) vs 2.448 .sup.3 for CH.sub.4 and 1.710 .sup.3 for N.sub.2) and quadrupole moment (4.30 D for CO.sub.2 vs 1.54 D and 0.02 D for N.sub.2 and CH.sub.4) of CO.sub.2 among the three gases which favors stronger physisorption interactions of CO.sub.2 than the other two adsorbents [See: Hanif, A.; Aziz, M. A.; Helal, A.; Abdelnaby, M. M.; Qasem, M. A. A.; Khan, A.; Hakeem, A. S.; Al-Betar, A. F.; Khan, M. Y. CO2 Adsorption on Pore-Engineered Carbons Derived from Jute Sticks. Chem. Asian J. 2023, 18, e202300481]. Further, CO.sub.2 is a weakly acidic gas and may interact with the basic N-atoms of the TPPM through weak acid-base interactions. Moreover, though N.sub.2 has a higher quadrupole moment than CH.sub.4, however, CH.sub.4 has higher polarizability than N.sub.2 which favors its adsorption over N.sub.2. For any gas, the adsorption decreases with increasing temperature also pointing to weak physisorption interactions existing between the adsorbate and adsorbent.

[0091] In the present disclosure, the synthesis and characterization of a new robust phenanthroline and triptycene units containing microporous polymer (TPPM) are described. The incorporation of rigid phenanthroline and 3D-triptycene motifs in TPPM provides desirable attributes such as abundant microporosity, high BET-specific surface area, and enhanced thermal stability. The polymer TPPM is microporous in nature and demonstrated a high SA.sub.BET of 1120 m.sup.2/g. All the aforementioned structural features in the polymer (TPPM) render it a promising material for efficient and selective CO.sub.2 uptakes. TPPM showed a high CO.sub.2 uptake of 2.76 mmol g.sup.1 at 273 K temperature. The CO.sub.2/N.sub.2 selectivity values at different temperatures were also observed to be reasonably high (20-28). Therefore, TPPM can be considered as a potentially useful material for environmental remediation applications considering its facile synthesis and capacity to efficiently and selectively capture CO.sub.2 over N.sub.2 and CH.sub.4. Considering TPPM's desirable structural features this study further encourages us and others to continue investigating and synthesizing phenanthroline-incorporated porous polymers linked with other rigid and aromatic motifs to enhance the sorbent properties for useful applications.

[0092] The design, synthesis, and characterization of a novel robust microporous polymer (TPPM) with phenanthroline and triptycene units are presented. The rigid phenanthroline and 3D-triptycene motifs in TPPM confer desirable attributes such as high microporosity, large BET-specific surface area, and improved thermal stability. The TPPM polymer is microporous and exhibits a high S.sub.ABET of 1120 m.sup.2/g. These structural features make TPPM a promising material for efficient and selective CO.sub.2 capture. TPPM has a high CO.sub.2 uptake of 2.76 mmol g.sup.1 at 273 K temperature. The CO.sub.2/N.sub.2 selectivity values at different temperatures are also reasonably high (20-28). Therefore, TPPM can be a potential material for environmental remediation applications due to its easy synthesis and ability to selectively and efficiently capture CO.sub.2 over N.sub.2 and CH4.

[0093] Numerous modifications and variations of the present disclosure are possible in light of the above teachings. Therefore, it is to be understood that within the scope of the appended claims, the invention may be practiced other than as specifically described herein.