Next Article in Journal
Selected Papers from the 1st International Online Conference on Nanomaterials
Next Article in Special Issue
Structural and Electrical Studies for Birnessite-Type Materials Synthesized by Solid-State Reactions
Previous Article in Journal
Low-Cost Localized Surface Plasmon Resonance Biosensing Platform with a Response Enhancement for Protein Detection
Previous Article in Special Issue
Growth and Functionalization of Particle-Based Mesoporous Silica Films and Their Usage in Catalysis
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Nanomaterials
Volume 9
Issue 7
10.3390/nano9071020
nanomaterials-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Communication

Synthesis of Porous Organic Polymers with Tunable Amine Loadings for CO2 Capture: Balanced Physisorption and Chemisorption

by
Xueying Kong
1,2,
Shangsiying Li
1,
Maria Strømme
2 and
Chao Xu
1,2,*
1
Key Laboratory of Flexible Electronics (KLOFE), Institute of Advanced Materials (IAM), Nanjing Tech University (Nanjing Tech), 30 South Puzhu Road, Nanjing 211800, China
2
Division of Nanotechnology and Functional Materials, Department of Engineering Sciences, Uppsala University, SE-75121 Uppsala, Sweden
*
Author to whom correspondence should be addressed.
Nanomaterials 2019, 9(7), 1020; https://doi.org/10.3390/nano9071020
Submission received: 1 July 2019 / Revised: 11 July 2019 / Accepted: 13 July 2019 / Published: 17 July 2019
(This article belongs to the Special Issue Functional Nanoporous Materials)
Browse Figures
Versions Notes

Abstract

:
The cross-coupling reaction of 1,3,5-triethynylbenzene with terephthaloyl chloride gives a novel ynone-linked porous organic polymer. Tethering alkyl amine species on the polymer induces chemisorption of CO2 as revealed by the studies of ex situ infrared spectroscopy. By tuning the amine loading content on the polymer, relatively high CO2 adsorption capacities, high CO2-over-N2 selectivity, and moderate isosteric heat (Qst) of adsorption of CO2 can be achieved. Such amine-modified polymers with balanced physisorption and chemisorption of CO2 are ideal sorbents for post-combustion capture of CO2 offering both high separation and high energy efficiencies.

Graphical Abstract

1. Introduction

The long-term increasing CO2 emission from combustion of fossil fuels is widely considered as the main reason for the global climate change and associated environmental issues [1]. Post-combustion carbon capture dealing with separation of CO2 from flue gases is a feasible approach to reduce industrial CO2 emissions and to gain control over the atmospheric CO2 concentration, and the method has the advantage of allowing quite simple retrofit design of required instrumentation into existing power plants [2]. However, the main challenge for the post-combustion technology is that the low concentration of CO2 (ca. 5%−15 v%) in flue gases usually results in low separation efficiency [3]. Amine scrubbing, a mature technique using aqueous amine solution to absorb CO2 from mixed gases, has been applied in natural gas purification and CO2 capture for more than a half century [4] and the technique is currently employed to create large scale pilot facilities in, amongst others, Norway [5]. The strong chemical interactions between amine and CO2 molecules endow the high efficiency for CO2 capture and separation. However, the energy consumption for amine reactivation arising from heating the aqueous amine solution is high. In addition, the use of amine might cause amine leakage and serious corrosion to the equipment. Therefore, it is highly desirable to develop new materials for post-combustion carbon capture that can be operated in an economical and environmentally friendly manner.
Porous materials with high surface areas and high volumes of narrow pores are ideal solid sorbents for adsorption-driven CO2 capture, in which CO2 molecules can be selectively adsorbed onto the surface or captured in the narrow pores [6,7]. For example, traditional zeolites and activated carbons have been extensively studied for CO2 capture owing to their high microporosities and relatively high CO2 adsorption capacities [8,9,10,11,12,13,14]. However, the hydrophilicity of zeolites and the broad pore size distributions of activated carbons have significantly limited their performances in CO2 capture and separation. Emerging porous materials such as metal−organic frameworks (MOFs) [15,16,17] and porous organic polymers (POPs) [18,19,20,21,22,23] are of great interest for CO2 capture because of their large surface areas and tunable pore sizes. POPs constitute a type of porous materials created by linking pure organic monomers, usually aromatic or conjugated, via strong covalent bonds [24,25]. The diverse synthesis possibilities of POPs allows precise control of their nanoporous structure and surface chemistry at the molecular level, aiming to increase the CO2 adsorption capacity and selectivity of CO2 over other gases by thermodynamic effects [26,27,28,29,30,31]. Several studies reported on post-modification of POPs with alkyl amines for CO2 capture [32,33,34,35,36,37,38,39]. The strong CO2−amine interactions on the amine-modified POPs led to significantly enhanced CO2 adsorption capacity and increased CO2-over-N2 selectivity. However, the strong interactions, interpreted by the high isosteric heat (Qst) of adsorption (up to 80 kJ mol−1) [35,37], require high energy input to reactivate the sorbents in the process of temperature swing adsorption (TSA) or vacuum swing adsorption (VSA) [40]. In this context, it would be great of interest to balance the trade-off between the separation efficiency and energy efficiency. Here, we report a strategy to tune the amine density on a novel ynone-linked POP (y-POP) by the post-modification approach, which enables balancing of the effects of physisorption and chemisorption of CO2 and optimization of the CO2 adsorption capacity, CO2-over-N2 selectivity and heat of adsorption of CO2.

2. Results and Discussion

POPs can be synthesized from various organic reactions, of which coupling reactions constitute the most commonly used routes [41]. For example, Zhu et al. reported on the Yamamoto homo-coupling reaction of tetrakis(4-bromophenyl)methane for the synthesis of a porous aromatic framework (PAF-1) [42]. The tetrahedral shaped monomer resulted in a three-dimensional framework of PAF-1 possessing an ultrahigh surface area of 5600 m2 g−1. Cooper and Jiang’s groups synthesized a number of conjugated microporous polymers (CMPs) by Suzuki, Sonogashira, and Glaser coupling reactions, which showed great potential in photocatalysis, light harvesting, etc. [43,44,45,46]. Recently, Son et al. developed a carbonylative Sonogashira coupling reaction of phenyl alkynes and phenyl halides in the presence of carbon monoxide, which gave a redox-active CMP that can be used as electrode material for electrochemical energy storage devices [47]. Therefore, the exploration of organic reactions to form novel structures in POPs could enrich their properties and applications. As we know, the cross-coupling reaction between terminal alkynes and acyl chloride under Sonogashira conditions forms conjugated α,β-alkynic ketones, also known as ynones [48]. More interestingly, further reaction of the ynones with alkyl amines could form imine compounds by two possible routes [48,49,50,51,52]. One is that of conjugate addition of the amine to α,β-alkynic ketone with formation of enaminone, which can be further converted into the imine compound via the nucleophilic addition in the presence of excess of amine. Another approach is direct nucleophilic addition of the amine to the ketone group forming the imine or enaminone compound. However, to the best of our knowledge, the direct coupling of terminal alkyne with acyl chloride has never been reported for the synthesis of POPs. In this context, we attempted the cross-coupling of 1,3,5-triethynylbenzene with terephthaloyl chloride under Sonogashira conditions for the synthesis of y-POP, which was catalyzed by bis(triphenylphosphine)palladium(II) dichloride and copper(I) iodide in the presence of trimethylamine as a base (Scheme 1a). The conjugated structure of the ynones and the aromatic monomers endow rigidity and stability of y-POP. In order to graft amine species onto the polymer, the as-synthesized y-POP was treated by tris(2-aminoethyl)amine (tren) in a methanol solution (Scheme 1b). The density of amine species tethered on the polymer was finely controlled by tuning the concentration of tren in the methanol solution. Specifically, treatment of y-POP in the methanol solution of tren (1, 5, 20 v%) yields the amine modified polymer y-POP-NH2, denoted as y-POP-A1, y-POP-A2, and y-POP-A3, respectively. Based on the thermogravimetric analyses (Figure S1), the amine loading content on the y-POP-NH2 can be roughly calculated to 12%, 16%, and 19% for y-POP-A1, y-POP-A2, and y-POP-A3, respectively.
The molecular structures of y-POP and y-POP-NH2 were examined by both Fourier transform infrared (IR) and solid-state 13C nuclear magnetic resonance (NMR) spectroscopy. The IR spectrum of y-POP shows strong bands at 2200 and 1720 cm−1, corresponding to the stretching vibrations of alkyne (−C≡C−) and carbonyl (−C=O), respectively (Figure 1a). In general, the central −C≡C− group with a high degree of symmetry displays a very weak IR stretching band [45]; however, the intensity of the IR band can be significantly increased by introducing conjugated structures [47,53]. Therefore, the intense IR band observed for the alkyne group can be correlated to the formation of conjugated structure with a carbonyl group (−C≡C(=O)−). The study of the solid-state 13C NMR spectrum also confirms the formation of ynone species in the polymer. The bands at chemical shifts of 91 and 83 ppm can be assigned to carbon atoms (1, 2) of alkyne bonds (Figure 1b and Figure S2). The characteristic band for carbon atoms (3) in carbonyl groups was observed at 176 ppm. Upon amine modification, the intensity of the IR band at 1720 cm−1 was gradually decreased with increasing amine loading, indicating that the carbonyl groups were consumed by the amine. In addition, the IR band intensity at 2200 cm−1 and NMR band intensity at 91 and 83 ppm were decreased in y-POP-NH2 compared to y-POP due to the transformation of the alkyne groups to enaminones. The broad shoulder bands at ~1660 cm−1 in the IR spectra of y-POP-NH2 can be assigned to the imine stretching vibrations. Consistently, the broad shoulder bands at the NMR chemical shift of 175−168 ppm for y-POP-NH2 indicate the formation of enamine and imine bonds [52,54]. The broad IR bands at 3370 cm−1 observed for y-POP-NH2 are assigned to the characteristic N−H stretching modes for the primary amine. The chemical shifts at 52 and 39 ppm for y-POP-NH2 correspond to the carbons in tethered tren species. The three major peaks at 137, 130 and 123 ppm are assigned to the aromatic carbons in y-POP and y-POP-NH2. Other peaks in the range of 60−10 ppm can be assigned to the carbon atoms in solvent molecules (tetrahydrofuran, methanol, triethylamine) adsorbed in the pores of y-POP. Collectively, the studies of the IR and 13C NMR spectra confirmed that ynone-linked POP was successfully synthesized and the tren molecules were chemically tethered on y-POP-NH2.
As a strong organic base with a pKb value ≈4, the tethered tren species on y-POP-NH2 could potentially attract CO2 molecules by the chemisorption effect. To investigate the CO2 adsorption mechanism, we designed an ex situ IR experiment to study the molecular interactions between CO2 and the polymers. The polymer sample was grinded with KBr and pressed into a transparent pellet, followed by drying at 100 °C for 12 h. The degassed pellet was used to record the IR background spectrum in a transmission model. The pellet was subsequently flashed with CO2 for 2 h at room temperature and thereafter a transmission IR spectrum was recorded again. The differences between the two spectra revealed the adsorbed CO2 on the polymers, as shown in Figure 2. The intense bands at frequencies of 2335 and 653 cm−1 in the spectra correspond to the physisorbed CO2 molecules, which can be assigned to the asymmetric stretching and deformation vibration of C=O, respectively [55]. Physisorption clearly dominates the CO2 adsorption on y-POP as no extra band was observed in the IR spectrum. In contrast, significant IR bands in the frequency region of 1750−1000 cm−1 were observed for y-POP-NH2, which indicates that the tethered amine species induced chemisorption of CO2. Obviously, a higher amine loading content in y-POP-NH2 resulted in a stronger IR intensity, suggesting the enhanced effect of chemisorption of CO2. The band at the frequency of 1704 cm−1 was assigned to C=O stretching (amide I), which is a characteristic indication of the formation of carbamic acid or carbamate species from the reaction between CO2 and the amine groups on y-POP-NH2 [56,57,58]. The broad band at 1243 cm−1 was assigned to a combination of N−H bending and C−N stretching (amide III) [59]. In addition, the bands at 1655, 1618, and 1475 cm−1 can be assigned to asymmetric deformation of NH3+ and the signals at 1538 and 1385 cm−1 can be associated to asymmetric stretching of COO− [55,60,61,62,63]. Therefore, we could speculate that chemisorption of CO2 on y-POP-NH2 forms ammonium carbamate ion pairs (Scheme S1).
The porosities of the polymers were analyzed by N2 sorption measurements at 77 K, as illustrated in Figure 3a. The sorption isotherm of y-POP displays rapid N2 adsorption at low relative pressures (p/p0 < 0.05), which is characteristic for microporous materials. The significant N2 uptake at high relative pressures (p/p0 > 0.8) and the accompanied hysteresis loop between the adsorption and desorption branches suggest the presence of mesopores in y-POP arising from the inter-particle cavities observed in SEM images (Figure S3). Such mesopores would facilitate the mass transportation and increase the adsorption kinetics during the sorption processes. Pore size distribution analyses showed that y-POP had ultramicropores (pore size: 0.74 nm), micropores (pore size: 1.2 nm) and mesopores (pore size: 34 nm). As expected, amine modification on y-POP resulted in disappearance of the ultramicropores and decrease in both micropore volumes and total pore volumes due to the pore blocking effect of the tren species (Figure 3b). Consistently, the specific surface area of the y-POP-NH2 was gradually decreased with increasing amine loading: the specific surface area values being 226, 145, 107, and 84 m2 g−1, for of y-POP, y-POP-A1, y-POP-A2, and y-POP-A3, respectively.
Given the microporous structure and the strong chemisorption of CO2 induced by the high amount of amine species, we anticipated that y-POP-NH2 would have much higher CO2 adsorption capacities and higher CO2-over-N2 selectivity than the corresponding values of unmodified y-POP. Figure 4a compares the CO2 adsorption isotherms of y-POP and y-POP-NH2 with different amine densities at 273 K. Although the specific surface areas of the polymers were reduced after the amine modification, y-POP-NH2 had significantly higher CO2 adsorption capacities than the substrate polymer of y-POP. With the increase of amine loading, the CO2 adsorption capacity of y-POP-NH2 gradually increased up to 1.11 and 1.88 mmol g−1 at 0.15 and 1 bar (273 K), respectively, which were 158% and 40% higher than the corresponding values of y-POP (0.43 mmol g−1 at 0.15 bar; 1.34 mmol g−1 at 1 bar, 273 K). In addition, the sorbents can be easily reactivated and showed excellent adsorption recyclability. For example, y-POP-A1 retained 97% of its CO2 adsorption capacity after 5 cycles at 293 K (Figure S6). In order to evaluate the potential of the polymers for capturing CO2 from flue gases, we calculated the CO2-over-N2 selectivity from their single component adsorption data recorded at 273 K (Figure 4a and Figure S7) using ideal adsorption solution theory (IAST) [13,35,64,65]. The CO2 and N2 adsorption isotherms were fitted by dual-site and single-site Langmuir equation, respectively (Figure S8 and Table S1). The CO2-over-N2 selectivity is defined as S = (xCO2/yCO2)/(xN2/yN2), where x and y are the molar fractions of the gas in the adsorbed and bulk phases, respectively. A simulated gas mixture of 15 v% CO2/85 v% N2 was used for the calculation. As illustrated in Figure 4b, the substrate polymer y-POP showed a relatively low CO2-over-N2 selectivity of 20. In contrast, y-POP-NH2 containing amine species displayed much higher selectivity up to 4.15 × 103. In addition, we have calculated Henry’s law initial slope selectivity for the polymers (Figure S9), which are comparable to the values obtained from the IAST calculations.
The binding affinity of the studied polymers toward CO2 was revealed by the Qst values, which can be calculated from the temperature dependent CO2 adsorption isotherms (273, 283, and 293 K) using the Clausius–Clapeyron equation. The substrate polymer of y-POP had a relatively low Qst value of 29.0 kJ mol−1, which is characteristic for the physisorption of CO2. As expected, y-POP-NH2 showed gradually increased Qst values (y-POP-A1: 46.8 kJ mol−1; y-POP-A2: 62.2 kJ mol−1; y-POP-A3: 76.5 kJ mol−1) with increasing amine loading (Figure S5). The high Qst values indicate the effect of chemisorption of CO2 on y-POP-NH2, which is consistence with the ex situ IR results.
Table 1 summarizes CO2 adsorption capacities, CO2-over-N2 selectivity, and Qst values for the four studied polymers. It is immediately clear that amine modification on the polymer significantly increases the efficiency for CO2 capture and separation due to the effect of chemisorption of CO2. In addition, the efficiency was proportional to the amine loading density on the polymer. However, the polymers containing high amine loading contents had relatively high Qst values, which means that reactivation of the sorbents requires a high energy consumption. Noteworthy, the sample y-POP-A1 had relatively high CO2 adsorption capacities (0.65 mmol g−1 at 0.15 bar; 1.50 mmol g−1; 273 K) and high CO2-over-N2 selectivity of 271 (273 K). The selectivity is comparable to some top-performing sorbents of amine-modified POPs [32], MOFs [66] and silica [67] that indicates the potential of using y-POP-A1 for efficient CO2 capture. In contrast, y-POP-A1 demonstrates a moderate Qst value of 46.8 kJ mol−1 at a low coverage of CO2 (0.2 mmol g−1), which is much lower than those of amine-modified sorbents (mmen-CuBTTri: 96 kJ mol−1; [66] PP1-2-tren: 80 kJ mol−1; [37] NTU-1: 75 kJ mol−1; [35] PEI (40 wt%) ⊂ PAF-5: 68.7 kJ mol−1 [38]; PPN-6-CH2-TETA: 63 kJ mol−1 [32]). Therefore, the balanced effects of physisorption and chemisorption of CO2 on y-POP-A1 would offer both high separation efficiency and high energy efficiency for post-combustion capture of CO2 from flue gases.

3. Conclusions

To conclude, a novel ynone-linked POP was synthesized and its molecular structure was fully characterized by IR and 13C NMR spectroscopy. The polymer was further used as a substrate to tether alkyl amine species by post modification. The ex situ IR results revealed that the amine species on the polymers could induce chemisorption of CO2 with formation of ammonium carbamate ion pairs. As a result, the amine-modified polymers showed high CO2 adsorption capacities, high CO2-over-N2 selectivity, as well as high Qst values. Remarkably, the amine density on the polymers can be finely controlled by a molecular engineering approach, which allows balancing the physisorption and chemisorption of CO2 to reach a high separation efficiency, excellent recyclability, high energy efficiency for CO2 capture and separation. The use of this strategy in the design of amine-modified porous solids (e.g., mesoporous silica, MOFs, clay, etc.) would offer highly efficient sorbents for post-combustion capture of CO2.

Supplementary Materials

The following are available online at https://www.mdpi.com/2079-4991/9/7/1020/s1. Figure S1. Thermogravimetric analysis curves of y-POP and y-POP-NH2. Figure S2. Solid-state 13C NMR spectra of y-POP, y-POP-A1, y-POP-A2, and y-POP-A3. Figure S3. SEM images of y-POP, y-POP-A1, y-POP-A2, and y-POP-A3. Figure S4. Powder X-ray diffraction patterns of y-POP and y-POP-NH2 showing the polymers are mainly amorphous. Figure S5. CO2 adsorption isotherms of y-POP, y-POP-A1, y-POP-A2, and y-POP-A3 recorded at 293 K. Figure S6. CO2 adsorption-desorption cycles for y-POP-A1 recorded at 293 K. Figure S7. N2 adsorption isotherms of y-POP, y-POP-A1, y-POP-A2, and y-POP-A3 recorded at 273 K. Figure S8. CO2 (■) and N2 (▲) adsorption data and of y-POP and y-POP-NH2 recorded at 273 K. The red solid lines show the fitting results of the data: The CO2 and N2 adsorption data was fitted by a dual-site and single-site Langmuir model, respectively. Detail fitting results are given in Table S1. The fitted parameters from the single adsorption data were used to predict the IAST selectivity. Figure S9. The CO2 and N2 adsorption data of (a) y-POP, (b) y-POP-A1, (c) y-POP-A2, and (d) y-POP-A3 at low partial pressures at 273 K and the linearly fitted results. Henry’s law CO2-over-N2 selectivities were calculated from the initial slopes of the CO2 and N2 isotherms. Table S1. Fitting parameters for the CO2 and N2 adsorption data recorded at 273 K. Scheme S1. Possible mechanism of chemisorption of CO2 on y-POP-NH2 with high amine loadings.

Author Contributions

X.K. and S.L. contributed equally to this work. Synthesis and characterization: X.K., S.L., C.X.; Data analysis: X.K., S.L., M.S., and C.X.; Writing: M.S. and C.X.

Funding

This research was funded by the Åforsk research grant, STINT (The Swedish Foundation for International Cooperation in Research and Higher Education) initiation grant, the Natural Science Foundation of Jiangsu Province (BK20170994), and the Natural Science Fund for Colleges and Universities in Jiangsu Province (17KJB430018).

Acknowledgments

We thank Samson Afewerki for valuable discussions.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Climate Change 2014: Synthesis Report; Contribution of Working Groups I, II and III to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change; IPCC: Geneva, Switzerland, 2014.
  2. Haszeldine, R.S. Carbon Capture and Storage: How Green Can Black Be? Science 2009, 325, 1647–1652. [Google Scholar] [CrossRef]
  3. Agarwal, A.; Biegler, L.T.; Zitney, S.E. A superstructure-based optimal synthesis of PSA cycles for post-combustion CO2 capture. AlChE J. 2010, 56, 1813–1828. [Google Scholar] [CrossRef]
  4. Rochelle, G.T. Amine scrubbing for CO2 capture. Science 2009, 325, 1652–1654. [Google Scholar] [CrossRef]
  5. CCS in Norway Entering a New Phase. Available online: https://www.gassnova.no/en/ccs-in-norway-entering-a-new-phase (accessed on 29 June 2018).
  6. D’Alessandro, D.M.; Smit, B.; Long, J.R. Carbon Dioxide Capture: Prospects for New Materials. Angew. Chem. Int. Ed. 2010, 49, 6058–6082. [Google Scholar] [CrossRef] [Green Version]
  7. Samanta, A.; Zhao, A.; Shimizu, G.K.H.; Sarkar, P.; Gupta, R. Post-Combustion CO2 Capture Using Solid Sorbents: A Review. Ind. Eng. Chem. Res. 2012, 51, 1438–1463. [Google Scholar] [CrossRef]
  8. Chue, K.T.; Kim, J.N.; Yoo, Y.J.; Cho, S.H.; Yang, R.T. Comparison of Activated Carbon and Zeolite 13X for CO2 Recovery from Flue Gas by Pressure Swing Adsorption. Ind. Eng. Chem. Res. 1995, 34, 591–598. [Google Scholar] [CrossRef]
  9. Zhao, J.; Xie, K.; Singh, R.; Xiao, G.; Gu, Q.; Zhao, Q.; Li, G.; Xiao, P.; Webley, P.A. Li+/ZSM-25 Zeolite as a CO2 Capture Adsorbent with High Selectivity and Improved Adsorption Kinetics, Showing CO2-Induced Framework Expansion. J. Phys. Chem. C 2018, 122, 18933–18941. [Google Scholar] [CrossRef]
  10. Jiang, Y.; Ling, J.; Xiao, P.; He, Y.; Zhao, Q.; Chu, Z.; Liu, Y.; Li, Z.; Webley, P.A. Simultaneous biogas purification and CO2 capture by vacuum swing adsorption using zeolite NaUSY. Chem. Eng. J. 2018, 334, 2593–2602. [Google Scholar] [CrossRef]
  11. Sethia, G.; Sayari, A. Comprehensive study of ultra-microporous nitrogen-doped activated carbon for CO2 capture. Carbon 2015, 93, 68–80. [Google Scholar] [CrossRef]
  12. Sevilla, M.; Mokaya, R.; Al-Jumialy, A.S.M.; Fuertes, A.B. Optimization of the Pore Structure of Biomass-Based Carbons in Relation to Their Use for CO2 Capture under Low- and High-Pressure Regimes. ACS Appl. Mater. Interfaces 2018, 10, 1623–1633. [Google Scholar] [CrossRef]
  13. Xu, C.; Ruan, C.-Q.; Li, Y.; Lindh, J.; Strømme, M. High-Performance Activated Carbons Synthesized from Nanocellulose for CO2 Capture and Extremely Selective Removal of Volatile Organic Compounds. Adv. Sustain. Syst. 2018, 2, 1700147. [Google Scholar] [CrossRef]
  14. Xu, C.; Strømme, M. Sustainable Porous Carbon Materials Derived from Wood-Based Biopolymers for CO2 Capture. Nanomaterials 2019, 9, 103. [Google Scholar] [CrossRef]
  15. Nugent, P.; Belmabkhout, Y.; Burd, S.D.; Cairns, A.J.; Luebke, R.; Forrest, K.; Pham, T.; Ma, S.; Space, B.; Wojtas, L.; et al. Porous materials with optimal adsorption thermodynamics and kinetics for CO2 separation. Nature 2013, 495, 80–84. [Google Scholar] [CrossRef]
  16. Xiang, S.; He, Y.; Zhang, Z.; Wu, H.; Zhou, W.; Krishna, R.; Chen, B. Microporous metal-organic framework with potential for carbon dioxide capture at ambient conditions. Nat. Commun. 2012, 3, 954. [Google Scholar] [CrossRef]
  17. McDonald, T.M.; Mason, J.A.; Kong, X.; Bloch, E.D.; Gygi, D.; Dani, A.; Crocellà, V.; Giordanino, F.; Odoh, S.O.; Drisdell, W.S.; et al. Cooperative insertion of CO2 in diamine-appended metal-organic frameworks. Nature 2015, 519, 303–308. [Google Scholar] [CrossRef]
  18. Chen, Q.; Luo, M.; Hammershøj, P.; Zhou, D.; Han, Y.; Laursen, B.W.; Yan, C.-G.; Han, B.-H. Microporous Polycarbazole with High Specific Surface Area for Gas Storage and Separation. J. Am. Chem. Soc. 2012, 134, 6084–6087. [Google Scholar] [CrossRef]
  19. Dawson, R.; Stöckel, E.; Holst, J.R.; Adams, D.J.; Cooper, A.I. Microporous organic polymers for carbon dioxide capture. Energy Environ. Sci. 2011, 4, 4239–4245. [Google Scholar] [CrossRef]
  20. Shan, M.; Liu, X.; Wang, X.; Yarulina, I.; Seoane, B.; Kapteijn, F.; Gascon, J. Facile manufacture of porous organic framework membranes for precombustion CO2 capture. Sci. Adv. 2018, 4, eaau1698. [Google Scholar] [CrossRef]
  21. Yan, J.; Zhang, B.; Wang, Z. Highly Selective Separation of CO2, CH4, and C2–C4 Hydrocarbons in Ultramicroporous Semicycloaliphatic Polyimides. ACS Appl. Mater. Interfaces 2018, 10, 26618–26627. [Google Scholar] [CrossRef]
  22. Gao, H.; Ding, L.; Bai, H.; Li, L. Microporous Organic Polymers Based on Hyper-Crosslinked Coal Tar: Preparation and Application for Gas Adsorption. ChemSusChem 2017, 10, 618–623. [Google Scholar] [CrossRef]
  23. Tan, M.X.; Zhang, Y.; Ying, J. Mesoporous Poly(Melamine-Formaldehyde) Solid Sorbent for Carbon Dioxide Capture. ChemSusChem 2013, 6, 1186–1190. [Google Scholar] [CrossRef]
  24. Xu, C.; Hedin, N. Microporous adsorbents for CO2 capture – a case for microporous polymers? Mater. Today 2014, 17, 397–403. [Google Scholar] [CrossRef]
  25. Chaoui, N.; Trunk, M.; Dawson, R.; Schmidt, J.; Thomas, A. Trends and challenges for microporous polymers. Chem. Soc. Rev. 2017, 46, 3302–3321. [Google Scholar] [CrossRef] [Green Version]
  26. Rabbani, M.G.; El-Kaderi, H.M. Template-Free Synthesis of a Highly Porous Benzimidazole-Linked Polymer for CO2Capture and H2Storage. Chem. Mater. 2011, 23, 1650–1653. [Google Scholar] [CrossRef]
  27. Lu, W.; Yuan, D.; Sculley, J.; Zhao, D.; Krishna, R.; Zhou, H.-C. Sulfonate-Grafted Porous Polymer Networks for Preferential CO2 Adsorption at Low Pressure. J. Am. Chem. Soc. 2011, 133, 18126–18129. [Google Scholar] [CrossRef]
  28. Xie, L.-H.; Suh, M.P.; Xie, L. High CO2-Capture Ability of a Porous Organic Polymer Bifunctionalized with Carboxy and Triazole Groups. Chem. A Eur. J. 2013, 19, 11590–11597. [Google Scholar] [CrossRef]
  29. Mohanty, P.; Kull, L.D.; Landskron, K. Porous covalent electron-rich organonitridic frameworks as highly selective sorbents for methane and carbon dioxide. Nat. Commun. 2011, 2, 401. [Google Scholar] [CrossRef]
  30. Dawson, R.; Cooper, A.I.; Adams, D.J. Chemical functionalization strategies for carbon dioxide capture in microporous organic polymers. Polym. Int. 2013, 62, 345–352. [Google Scholar] [CrossRef]
  31. Haikal, R.R.; Hassan, Y.S.; Emwas, A.-H.; Belmabkhout, Y.; Alkordi, M.H. Poly-functional porous-organic polymers to access functionality—CO2 sorption energetic relationships. J. Mater. Chem. A 2015, 3, 22584–22590. [Google Scholar]
  32. Lu, W.; Sculley, J.P.; Yuan, D.; Krishna, R.; Wei, Z.; Zhou, H.-C. Polyamine-Tethered Porous Polymer Networks for Carbon Dioxide Capture from Flue Gas. Angew. Chem. Int. Ed. 2012, 51, 7480–7484. [Google Scholar] [CrossRef]
  33. Guillerm, V.; Weselinski, L.J.; Alkordi, M.; Mohideen, M.I.H.; Belmabkhout, Y.; Cairns, A.J.; Eddaoudi, M. Porous organic polymers with anchored aldehydes: A new platform for post-synthetic amine functionalization en route for enhanced CO2 adsorption properties. Chem. Commun. 2014, 50, 1937. [Google Scholar] [CrossRef]
  34. Ratvijitvech, T.; Dawson, R.; Laybourn, A.; Khimyak, Y.Z.; Adams, D.J.; Cooper, A.I. Post-synthetic modification of conjugated microporous polymers. Polymer 2014, 55, 321–325. [Google Scholar] [CrossRef]
  35. Sun, L.-B.; Kang, Y.-H.; Shi, Y.-Q.; Jiang, Y.; Liu, X.-Q. Highly Selective Capture of the Greenhouse Gas CO2 in Polymers. ACS Sustain. Chem. Eng. 2015, 3, 3077–3085. [Google Scholar] [CrossRef]
  36. Puthiaraj, P.; Lee, Y.-R.; Ahn, W.-S. Microporous amine-functionalized aromatic polymers and their carbonized products for CO2 adsorption. Chem. Eng. J. 2017, 319, 65–74. [Google Scholar] [CrossRef]
  37. Xu, C.; Bacsik, Z.; Hedin, N. Adsorption of CO2 on a micro-/mesoporous polyimine modified with tris(2-aminoethyl)amine. J. Mater. Chem. A 2015, 3, 16229–16234. [Google Scholar] [CrossRef]
  38. Sung, S.; Suh, M.P. Highly efficient carbon dioxide capture with a porous organic polymer impregnated with polyethylenimine. J. Mater. Chem. A 2014, 2, 13245–13249. [Google Scholar] [CrossRef]
  39. Lu, W.; Sculley, J.P.; Yuan, D.; Krishna, R.; Zhou, H.-C. Carbon Dioxide Capture from Air Using Amine-Grafted Porous Polymer Networks. J. Phys. Chem. C 2013, 117, 4057–4061. [Google Scholar] [CrossRef]
  40. Hedin, N.; Andersson, L.; Bergström, L.; Yan, J. Adsorbents for the post-combustion capture of CO2 using rapid temperature swing or vacuum swing adsorption. Appl. Energy 2013, 104, 418–433. [Google Scholar] [CrossRef]
  41. Xu, Y.; Jin, S.; Xu, H.; Nagai, A.; Jiang, D. Conjugated microporous polymers: Design, synthesis and application. Chem. Soc. Rev. 2013, 42, 8012. [Google Scholar] [CrossRef]
  42. Ben, T.; Ren, H.; Ma, S.; Cao, D.; Lan, J.; Jing, X.; Wang, W.; Xu, J.; Deng, F.; Simmons, J.M.; et al. Targeted Synthesis of a Porous Aromatic Framework with High Stability and Exceptionally High Surface Area. Angew. Chem. Int. Ed. 2009, 48, 9457–9460. [Google Scholar] [CrossRef]
  43. Sprick, R.S.; Jiang, J.-X.; Bonillo, B.; Ren, S.; Ratvijitvech, T.; Guiglion, P.; Zwijnenburg, M.A.; Adams, D.J.; Cooper, A.I. Tunable Organic Photocatalysts for Visible-Light-Driven Hydrogen Evolution. J. Am. Chem. Soc. 2015, 137, 3265–3270. [Google Scholar] [CrossRef]
  44. Chen, L.; Honsho, Y.; Seki, S.; Jiang, D. Light-Harvesting Conjugated Microporous Polymers: Rapid and Highly Efficient Flow of Light Energy with a Porous Polyphenylene Framework as Antenna. J. Am. Chem. Soc. 2010, 132, 6742–6748. [Google Scholar] [CrossRef]
  45. Jiang, J.-X.; Su, F.; Niu, H.; Wood, C.D.; Campbell, N.L.; Khimyak, Y.Z.; Cooper, A.I. Conjugated microporous poly(phenylene butadiynylene)s. Chem. Commun. 2008, 486–488. [Google Scholar] [CrossRef]
  46. Jiang, J.-X.; Su, F.; Trewin, A.; Wood, C.D.; Campbell, N.L.; Niu, H.; Dickinson, C.; Ganin, A.Y.; Rosseinsky, M.J.; Khimyak, Y.Z.; et al. Conjugated Microporous Poly(aryleneethynylene) Networks. Angew. Chem. Int. Ed. 2007, 46, 8574–8578. [Google Scholar] [CrossRef]
  47. Choi, J.; Ko, J.H.; Kang, C.W.; Lee, S.M.; Kim, H.J.; Ko, Y.-J.; Yang, M.; Son, S.U. Enhanced redox activity of a hollow conjugated microporous polymer through the generation of carbonyl groups by carbonylative Sonogashira coupling. J. Mater. Chem. A 2018, 6, 6233–6237. [Google Scholar] [CrossRef]
  48. Karabiyikoglu, S.; Kelgokmen, Y.; Zora, M. Facile synthesis of iodopyridines from N-propargylic β-enaminones via iodine-mediated electrophilic cyclization. Tetrahedron 2015, 71, 4324–4333. [Google Scholar] [CrossRef]
  49. Kelgokmen, Y.; Zora, M. Facile synthesis of heavily-substituted alkynylpyridines via a Sonogashira approach. RSC Adv. 2016, 6, 4608–4621. [Google Scholar] [CrossRef]
  50. Hoven, B.G.V.D.; Alper, H. Innovative Synthesis of 4-Carbaldehydepyrrolin-2-ones by Zwitterionic Rhodium Catalyzed Chemo- and Regioselective Tandem Cyclohydrocarbonylation/CO Insertion of α-Imino Alkynes. J. Am. Chem. Soc. 2001, 123, 10214–10220. [Google Scholar] [CrossRef]
  51. Waldo, J.P.; LaRock, R.C. The Synthesis of Highly Substituted Isoxazoles by Electrophilic Cyclization. An Efficient Synthesis of Valdecoxib. J. Org. Chem. 2007, 72, 9643–9647. [Google Scholar] [CrossRef]
  52. Liu, X.; Hong, D.; She, Z.; Hersh, W.H.; Yoo, B.; Chen, Y. Complementary regioselective synthesis of 3,5-disubstituted isoxazoles from ynones. Tetrahedron 2018, 74, 6593–6606. [Google Scholar] [CrossRef]
  53. Socrates, G. Infrared and Raman Characteristic Group Frequencies: Tables and Charts; John Wiley & Sons: Hoboken, NJ, USA, 2004. [Google Scholar]
  54. Xu, C.; Hedin, N. Synthesis of microporous organic polymers with high CO2-over-N2 selectivity and CO2 adsorption. J. Mater. Chem. A 2013, 1, 3406. [Google Scholar] [CrossRef]
  55. Bacsik, Z.; Atluri, R.; Garcia-Bennett, A.E.; Hedin, N. Temperature-Induced Uptake of CO2 and Formation of Carbamates in Mesocaged Silica Modified with n-Propylamines. Langmuir 2010, 26, 10013–10024. [Google Scholar] [CrossRef]
  56. Knoöfel, C.; Martin, C.; Hornebecq, V.; Llewellyn, P.L. Study of Carbon Dioxide Adsorption on Mesoporous Aminopropylsilane-Functionalized Silica and Titania Combining Microcalorimetry and in Situ Infrared Spectroscopy. J. Phys. Chem. C 2009, 113, 21726–21734. [Google Scholar]
  57. Danon, A.; Stair, P.C.; Weitz, E. FTIR Study of CO2 Adsorption on Amine-Grafted SBA-15: Elucidation of Adsorbed Species. J. Phys. Chem. C 2011, 115, 11540–11549. [Google Scholar] [CrossRef]
  58. Aziz, B.; Hedin, N.; Bacsik, Z. Quantification of chemisorption and physisorption of carbon dioxide on porous silica modified by propylamines: Effect of amine density. Micropor. Mesopor. Mater. 2012, 159, 42–49. [Google Scholar] [CrossRef]
  59. Fu, F.-N.; DeOliveira, D.B.; Trumble, W.R.; Sarkar, H.K.; Singh, B.R. Secondary Structure Estimation of Proteins Using the Amide III Region of Fourier Transform Infrared Spectroscopy: Application to Analyze Calcium-Binding-Induced Structural Changes in Calsequestrin. Appl. Spectrosc. 1994, 48, 1432–1441. [Google Scholar] [CrossRef]
  60. Wang, X.; Schwartz, V.; Clark, J.C.; Ma, X.; Overbury, S.H.; Xu, X.; Song, C. Infrared Study of CO2 Sorption over “Molecular Basket” Sorbent Consisting of Polyethylenimine-Modified Mesoporous Molecular Sieve. J. Phys. Chem. C 2009, 113, 7260–7268. [Google Scholar] [CrossRef]
  61. Hiyoshi, N.; Yogo, K.; Yashima, T. Adsorption characteristics of carbon dioxide on organically functionalized SBA-15. Micropor. Mesopor. Mater. 2005, 84, 357–365. [Google Scholar] [CrossRef]
  62. Bacsik, Z.; Ahlsten, N.; Ziadi, A.; Zhao, G.; Garcia-Bennett, A.E.; Martín-Matute, B.; Hedin, N. Mechanisms and Kinetics for Sorption of CO2 on Bicontinuous Mesoporous Silica Modified with n-Propylamine. Langmuir 2011, 27, 11118–11128. [Google Scholar] [CrossRef]
  63. Huang, H.Y.; Yang, R.T.; Chinn, D.; Munson, C.L. Amine-Grafted MCM-48 and Silica Xerogel as Superior Sorbents for Acidic Gas Removal from Natural Gas. Ind. Eng. Chem. Res. 2003, 42, 2427–2433. [Google Scholar] [CrossRef]
  64. Myers, A.L.; Prausnitz, J.M. Thermodynamics of mixed-gas adsorption. AIChE J. 1965, 11, 121–127. [Google Scholar] [CrossRef]
  65. Patel, H.H.A.; Byun, J.; Yavuz, C.T. Carbon Dioxide Capture Adsorbents: Chemistry and Methods. ChemSusChem 2017, 10, 1303–1317. [Google Scholar] [CrossRef] [PubMed]
  66. McDonald, T.M.; D’Alessandro, D.M.; Krishna, R.; Long, J.R. Enhanced carbon dioxide capture upon incorporation of N,N′-dimethylethylenediamine in the metal–organic framework CuBTTri. Chem. Sci. 2011, 2, 2022–2028. [Google Scholar] [CrossRef]
  67. Choi, S.; Gray, M.L.; Jones, C.W. Amine-Tethered Solid Adsorbents Coupling High Adsorption Capacity and Regenerability for CO2 Capture from Ambient Air. ChemSusChem 2011, 4, 628–635. [Google Scholar] [CrossRef] [PubMed]
Nanomaterials 09 01020 sch001 550
Scheme 1. (a) Synthesis of ynone-linked porous organic polymer (y-POP) by the Sonogashira coupling reaction; (b) amine modification of y-POP.
Scheme 1. (a) Synthesis of ynone-linked porous organic polymer (y-POP) by the Sonogashira coupling reaction; (b) amine modification of y-POP.
Nanomaterials 09 01020 sch001
Nanomaterials 09 01020 g001 550
Figure 1. (a) Infrared (IR) and (b) 13C nuclear magnetic resonance (NMR) spectra of ynone-linked porous organic polymer (y-POP) and y-POP-NH2.
Figure 1. (a) Infrared (IR) and (b) 13C nuclear magnetic resonance (NMR) spectra of ynone-linked porous organic polymer (y-POP) and y-POP-NH2.
Nanomaterials 09 01020 g001
Nanomaterials 09 01020 g002 550
Figure 2. Infrared (IR) spectra of adsorbed CO2 on ynone-linked porous organic polymer (y-POP) and y-POP-NH2.
Figure 2. Infrared (IR) spectra of adsorbed CO2 on ynone-linked porous organic polymer (y-POP) and y-POP-NH2.
Nanomaterials 09 01020 g002
Nanomaterials 09 01020 g003 550
Figure 3. (a) N2 adsorption/desorption isotherms of ynone-linked porous organic polymer (y-POP) and y-POP-NH2 recorded at 77 K; (b) Pore size distribution analyses of y-POP and y-POP-NH2 based on the adsorption branches using the density functional theory model.
Figure 3. (a) N2 adsorption/desorption isotherms of ynone-linked porous organic polymer (y-POP) and y-POP-NH2 recorded at 77 K; (b) Pore size distribution analyses of y-POP and y-POP-NH2 based on the adsorption branches using the density functional theory model.
Nanomaterials 09 01020 g003
Nanomaterials 09 01020 g004 550
Figure 4. (a) CO2 adsorption isotherms of ynone-linked porous organic polymer (y-POP) and y-POP-NH2 with different amine loadings at 273 K; (b) CO2-over-N2 selectivity of y-POP and y-POP-NH2 calculated by ideal adsorbed solution theory.
Figure 4. (a) CO2 adsorption isotherms of ynone-linked porous organic polymer (y-POP) and y-POP-NH2 with different amine loadings at 273 K; (b) CO2-over-N2 selectivity of y-POP and y-POP-NH2 calculated by ideal adsorbed solution theory.
Nanomaterials 09 01020 g004
Table
Table 1. A summary of specific surface area (SBET), CO2 adsorption capacity (273 K), CO2-over-N2 selectivity (273 K), and Qst of CO2 adsorption at the low coverage of CO2 for ynone-linked porous organic polymer (y-POP) and y-POP-NH2 with different amine densities.
Table 1. A summary of specific surface area (SBET), CO2 adsorption capacity (273 K), CO2-over-N2 selectivity (273 K), and Qst of CO2 adsorption at the low coverage of CO2 for ynone-linked porous organic polymer (y-POP) and y-POP-NH2 with different amine densities.
SampleAmine LoadingSBET
(m2 g−1)		CO2 Uptake (mmol g−1)CO2/N2 SelectivityQst
(kJ mol−1)
0.15 bar1 barIASTHenry’s Law
y-POP02260.431.34202229.0
y-POP-A112%1450.651.5023921646.8
y-POP-A216%1070.761.49108375062.2
y-POP-A319%841.111.954154380676.5

Share and Cite

MDPI and ACS Style

Kong, X.; Li, S.; Strømme, M.; Xu, C. Synthesis of Porous Organic Polymers with Tunable Amine Loadings for CO2 Capture: Balanced Physisorption and Chemisorption. Nanomaterials 2019, 9, 1020. https://doi.org/10.3390/nano9071020

AMA Style

Kong X, Li S, Strømme M, Xu C. Synthesis of Porous Organic Polymers with Tunable Amine Loadings for CO2 Capture: Balanced Physisorption and Chemisorption. Nanomaterials. 2019; 9(7):1020. https://doi.org/10.3390/nano9071020

Chicago/Turabian Style

Kong, Xueying, Shangsiying Li, Maria Strømme, and Chao Xu. 2019. "Synthesis of Porous Organic Polymers with Tunable Amine Loadings for CO2 Capture: Balanced Physisorption and Chemisorption" Nanomaterials 9, no. 7: 1020. https://doi.org/10.3390/nano9071020

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop