Ultramicroporous material based parallel and extended paraffin nano

Nature Communications volume 13, Article number: 4928 (2022) Cite this article

4592 Accesses

10 Citations

1 Altmetric

Metrics details

Selective paraffin capture from olefin/paraffin mixtures could afford high-purity olefins directly, but suffers from the issues of low separation selectivity and olefin productivity. Herein, we report an ultramicroporous material (PCP-IPA) with parallel-aligned linearly extending isophthalic acid units along the one-dimensional channel, realizing the efficient production of ultra-high purity C2H4 and C3H6 (99.99%). The periodically expanded and parallel-aligned aromatic-based units served as a paraffin nano-trap to contact with the exposed hydrogen atoms of both C2H6 and C3H8, as demonstrated by the simulation studies. PCP-IPA exhibits record separation selectivity of 2.48 and separation potential of 1.20 mol/L for C3H8/C3H6 (50/50) mixture, meanwhile the excellent C2H6/C2H4 mixture separation performance. Ultra-high purity C3H6 (99.99%) and C2H4 (99.99%) can be directly obtained through fixed-bed column from C3H8/C3H6 and C2H6/C2H4 mixtures, respectively. The record C3H6 productivity is up to 15.23 L/kg from the equimolar of C3H8/C3H6, which is 3.85 times of the previous benchmark material, demonstrating its great potential for those important industrial separations.

Olefins (e.g., propylene and ethylene) are important chemical feedstocks in petrochemical industry, and at least polymer-grade or even the ultra-high purity (99.99%) olefins are required for the manufacture of advanced fine chemicals and polymers1,2. Olefin/paraffin separation is the key process to afford high purity olefins, but is mainly carried out via cryogenic distillation that is associated with high energy footprints, or even the multistep distillation3,4,5. The development of non-thermal driven alternatives with low carbon emissions are the potential solutions to the challenges5,6.

Adsorptive separation technologies based on porous materials provide a feasible avenue to solve the dilemma, and the technologies show more attractive prospects with the continuous progress in tailor-made porous materials7,8,9,10,11,12,13,14. Olefin-selective adsorbents have been widely explored for olefin/paraffin separation with considerable achievements15,16,17,18,19,20,21,22,23,24. However, even the current benchmark molecular-sieving material with ideally infinite olefin/paraffin selectivity could only afford olefins with purity of 99.1% due to the inevitable coadoption of paraffins, and extra adsorption–desorption cycles are necessary for olefins to reach polymer-grade purity17. It is rationally speculated that the purification steps would be more complex to produce olefins with ultra-high purity (99.99%)25,26. By contrast, paraffin-selective adsorbents are advantaged in directly affording high-purity olefins via only single adsorption cycle, simplifying the separation process, and gradually attract the interests27,28,29,30. For example, Hartmann et al. reported two Zeolite imidazolate frameworks (ZIF-4 and ZIF-8) showed stronger affinity toward alkanes than alkenes31,32, Jorge et al. proved that ZIF-7 could selectivity adsorbed alkanes over alkenes through gate-opening effect33, and Anne et al. predicted Silicalite-1 possess paraffin-selective adsorption performance34. As evidence of the reported paraffin-selective adsorbents, there are two ways to realize the selective adsorption of alkanes. (1) Through the construction of specific functional sites and the control of functional sites distribution to form multiple hydrogen-bond with paraffins, such as the iron-peroxo sites of Fe(O2)(dobdc)35, the precise N and O distribution of MAF-4936 and JNU-237, etc.38,39, exhibit higher affinity to C2H6 than C2H4. (2) Enriching with the nonpolar surfaces of pore structure to recognize the paraffins and olefins properties difference of quadrupole moment, like BUT-1040, PCN-25041, Cu(Qc)242, HOF-7643, and etc.44,45,46,47. However, most of these paraffin-selective adsorbents design approaches are based on the three dimensions of pore to match the size of paraffins, it reversely causes the inefficiency of single material to simultaneously identify C2H6 and C3H8 with different molecular size (Fig. 1a). In addition, though the remarkable progress in the design, both separation selectivity and olefin productivity of the current paraffin-selective adsorbents are still to be improved, especially for C3H8/C3H6 mixture, the paraffin/olefin selectivity is below 2, and the olefin productivity is lower than 4.0 L/kg40,48,49,50.

Considering the preferential paraffin adsorption behavior is dominated by the interactions between the hydrogen atoms of paraffins and the framework, and the similar structural conformation of C2H6 and C3H8 in the specific orientation with both side-distributed hydrogen atoms that are easily accessible, a parallel and extended paraffin nano-trap would be favored for paraffin accommodation via the close and dense contact with the hydrogen atoms (Fig. 1b). Herein, we reveal that the ultramicroporous material [Co(IPA)(DPG)]n (PCP-IPA; PCP = Porous coordination polymer, IPA = isophthalic acid, DPG = meso-α, β-di(4-pyridyl) glycol) featuring with parallel-aligned linearly extending isophthalic acid units sets a new benchmark for paraffin/olefin separations. The unique pore size and environment enables the directional adsorption of C2H6 and C3H8 through the rigidly bounded between their aligned hydrogen atoms and the closely parallel-aligned isophthalic acid units, realizing the simultaneous efficient separation of both C2 and C3 paraffin/olefin mixtures. PCP-IPA exhibits the record C3H8/C3H6 selectivity of 2.48 and separation potential of 1.20 mol/L for C3H8/C3H6 (50/50) mixtures, as well as the excellent C2H6/C2H4 separation performance. Ultra-high purity C3H6 (99.99%) and C2H4 (99.99%) are obtained through the breakthrough experiment using PCP-IPA from C3H8/C3H6 and C2H6/C2H4 mixture, respectively. The record C3H6 productivity is up to 15.23 L/kg from the equimolar of C3H8/C3H6, 3.85 times of the previous benchmark material. The molecular-level insight into the paraffin and olefin adsorption behaviors are further revealed by simulation studies.

The reaction of meso-α, β-di(4-pyridyl) glycol (DPG), and isophthalic acid (IPA) with Co(NO3)2·6H2O afforded PCP-IPA51. Individually, in PCP-IPA, each Co(II) atom is six coordinated in an octahedral geometry, and the coordination between the Co atoms and two N atoms from the pyridine ring, two O atoms from the hydroxyl group of the DPG ligand forms a 2D layer network (Supplementary Fig. 2). The adjacent 2D layer networks are pillared with the IPA ligands to afford a 3D pillared layered framework with one-dimensional straight channel (Fig. 1c, d). The channel is featured with the parallel-aligned linearly extending isophthalic acid units, and the pore window of PCP-IPA is estimated to be 4.7 × 5.6 Å2, which is suitable for the accommodation of paraffins. Benefiting from the big π system and hydrogen bond acceptor provided by the aromatic units and uncoordinated negatively charged oxygen atoms, the channel is anticipated to be an efficient paraffin nano-trap. The experimental PXRD pattern of PCP-IPA matches well with the simulated one, confirming the high phase-purity of as-synthesized PCP-IPA (Supplementary Fig. 3). PCP-IPA shows good thermal stability up to 280 °C (Supplementary Fig. 4). The permanent pore structure of PCP-IPA is investigated by 195 K CO2 adsorption–desorption isotherm (Supplementary Fig. 5), and the Langmuir-specific surface area and pore volume of PCP-IPA are determined as 486.7 m2/g and 0.19 cm3/g, respectively. Furthermore, the other basic characterization of SEM and FT-IR on PCP-IPA shown as Supplementary Figs. 6 and 7.

a Schematic illustration of the common paraffin-trap channel, b schematic illustration of the parallel and extended paraffin nano-trap channel, (c) the building blocks (CoII, DPG, and IPA organic ligand) and the 3D network topology of PCP-IPA, d the 1D channel structure of PCP-IPA (C, orange or grey-80%; H, white; N, blue; O, red; Co, light blue).

The single-component adsorption isotherms were conducted to explore the paraffin/olefin separation performance of PCP-IPA (Fig. 2a and Supplementary Fig. 8). As expected, PCP-IPA exhibits remarkable paraffin-selective adsorption during the whole pressure range (0–1.0 bar). It sets a new benchmark IAST (Ideal adsorbed solution theory) selectivity for C3H8/C3H6 (50/50) up to 2.48 at 1.0 bar and 298 K (Fig. 2b), greater than the previously reported top-performing porous materials, such as NUM-7a (1.80)50, WOFOUR-1-Ni (1.60)48, CPM-734c (1.44)49, and BTU-10 (1.40)40 (Fig. 2c). Furthermore, the C3H8/C3H6 (50/50) separation potential (△Q) that based on the combined effect of adsorption capacity and selectivity for separation performance prediction is revealed, and PCP-IPA also exhibits the record value, up to 1.20 mol/L (1.0 bar), 1.3 times to the previous benchmarks NUM-7a (0.93 mol/L) (Fig. 2d). Meanwhile, high separation selectivity up to 2.80 and separation potential (△Q) for C2H6/C2H4 (50/50) mixture are also observed on PCP-IPA (Fig. 2e), highlighting the great separation potential of PCP-IPA for both C3H8/C3H6 and C2H6/C2H4 mixtures52,53,54,55. The higher affinity of paraffins to olefins is also verified by the calculated adsorption heat Qst (C3H8 50.94 kJ/mol vs 43.36 kJ/mol, C2H6 37.73 kJ/mol vs C2H4 27.48 kJ/mol) (Supplementary Figs. 9 and 10). The kinetic effect is regarded as a great hindrance to prevent preferential paraffin adsorption behavior, and gas diffusion is a critical factor in ultramicroporous adsorbent for real industrial applications, the time-dependent gas uptake profiles of C3H8, C3H6, C2H6, and C2H4 were measured. The results show that the diffusion rates of all gases in the channel are fast and there are no kinetic difference between paraffins and olefins (Fig. 2f and Supplementary Fig. 12), demonstrating the suitable pore size of PCP-IPA.

a The C3H8, C3H6, C2H6, and C2H4 adsorption isotherms at 298 K; b IAST selectivity (c) comparison plot of C3H8/C3H6 (50/50 v/v) IAST selectivity among benchmark materials; comparison of PCP-IPA separation potential (ΔQ IAST) with reported benchmark MOFs based on IAST calculation from d C3H8/C3H6 (50/50 v/v) mixtures and e C2H6/C2H4 (50/50 v/v) mixtures. f Time-dependent gas uptake profiles of C3H8 at 50 mbar and 298 K.

To understand the molecular-level paraffin and olefin adsorption behavior within the channel of PCP-IPA, we performed detailed modeling studies using first-principles dispersion-corrected density functional theory (DFT-D) method. As shown in Fig. 3, the paraffins prefer the adsorbed orientation that the section of the molecules is vertical to the extending direction of the channel, and the parallel-aligned isophthalic acid units are served as the tailored binding environment for the lined hydrogen atoms of paraffins. Despite the different molecular lengths, C2H6 and C3H8 could collect enough binding sites along the extending isophthalic acid units, allowing PCP-IPA to have both high C3H8 and C2H6 affinity. Meanwhile, the pore structure of parallel-aligned linearly extending aromatic units as well as the appropriate distance between parallel benzene rings also give full play of the advantages of paraffins to olefins, the more C-H binding sites and large molecular size. Paraffins exhibit more dense interactions with the isophthalic acid units than olefins, which are also supported by the calculated binding energies of C3H8 (−54.01 kJ/mol), C3H6 (−50.32 kJ/mol), C2H6 (−39.36 kJ/mol), and C2H4 (−35.24 kJ/mol). In detail, each C3H8 molecule interacts with three phenyl rings and three uncoordinated oxygen atoms to form multiple van der Waals forces (eleven C-H•••C 2.83–3.21 Å) and three C-H•••O H-bonding interactions (C-H•••O 2.76–3.20 Å) (Fig. 3a). In contrast, the C3H6 molecule shows only one C-H•••O H-bonding interaction (C-H•••O 2.51 Å), and seven C-H•••C van der Waals forces (C-H•••C 2.80–3.16 Å) with framework (Fig. 3b). C2H6 shows the similar adsorption behavior, and is rigidly bounded by the more C-H•••C and C-H•••O interactions than C2H4 (Fig. 3c, d). The simulation studies reveal that the parallel-lined and linear-extending aromatic units could provide enough binding sites toward paraffins even with different molecular size thanks to the specific adsorbed orientation.

a C3H8, b C3H6, c C2H6, and d C2H4 binding sites in PCP-IPA. The closest contacts between framework atoms and the gas molecules are defined by the distances (in Å) and the distances include the Van der Waals radius of atoms. (Framework: C, gray-80%; H, white; N, blue; O, red; Co, light blue; Gas: C, orange; H, white).

Furthermore, the dynamic transient breakthrough experiments were conducted to evaluate the actual separation ability of PCP-IPA for paraffin/olefin mixtures, and highly efficient separation performance is observed for both C2 and C3 paraffin/olefin separations. As the C3H8/C3H6 (50/50, v/v) mixture flows through the column packed with PCP-IPA, C3H6 is first eluted at the time of 34.8 min while C3H8 is continuously adsorbed until the time of 43.9 min (Fig. 4a). During the above time gap (34.8–43.9 min), ultra-high purity C3H6 (99.99%) can be collected with the record C3H6 productivity of 15.23 L/kg. The productivity is nearly four times that of the pervious benchmark material BUT-10 (3.95 L/kg)40 and WOFOUR-1-Ni (3.50 L/kg)48 under the same conditions. For C3H8/C3H6 mixtures with only 5% C3H8, we are still able to collect the 99.99% C3H6 and high C3H6 productivity of 30.06 L/kg, demonstrating the broad applicability of PCP-IPA for paraffin/olefin mixtures of different compositions. Consistent with the adsorption isotherms and simulation studies, PCP-IPA also shows remarkable C2H6/C2H4 separation performance and the corresponding C2H4 productivity is 26.2 L/kg, rendering it to be one of the leading materials for C2H6-selective adsorbents. In addition, we find that the paraffin working capacity of PCP-IPA calculated by breakthrough curves is close to the static adsorption capacity (C2H6, 2.10 vs 2.24 mmol/g; C3H8, 1.81 vs 2.16 mmol/g), further verifying the rapid diffusion behavior of paraffins and olefins within the channel (Supplementary Tables 6 and 7). We evaluate the influence of water vapor on the separation ability of PCP-IPA, and no decrease is observed on the breakthrough performance (Fig. 4c and Supplementary Fig. 18a). During the 14 cycling tests, the separation performance is well maintained (Fig. 4f, Supplementary Figs. 19–21 and Table 8). Meanwhile, PCP-IPA is also highly resistant to air and water, and both the XRD patterns and C2H6 capacity remain unchanged after treatment (Supplementary Fig. 17). The adsorption column could be regenerated rapidly and completely within 60 min and 45 min for C2 and C3 mixtures, respectively, under 333 K and 373 K with the purging N2 flow rate of 10 mL/min (Supplementary Figs. 22 and 23). The impressive separation performance and the good stability of PCP-IPA highlight its great promise in paraffin/olefin separations.

Dynamic breakthrough curves under 298 K and 1.0 bar of a C3H8/C3H6 (50/50 v/v) mixture, b C3H8/C3H6 (5/95 v/v) mixture, and c C2H6/C2H4 (50/50 v/v) with (hollow) or without water vapor (solid); comparison of high pure olefin productivity on PCP-IPA with reported benchmark materials for d C3H8/C3H6 (50/50 v/v) mixture and e C2H6/C2H4 (50/50 v/v) mixture; f recycling breakthrough tests for C3H8/C3H6 (5/95 v/v, red, 2.20 mL/min), C3H8/C3H6 (50/50 v/v, blue, 1.10 mL/min), C3H8/C3H6 (50/50 v/v, cyan, 2.20 mL/min) and C2H6/C2H4 (50/50 v/v, orange, 3.7 mL/min) separation with PCP-IPA under 298 K and 1.0 bar.

In summary, we have discovered a distinctive ultramicroporous material featuring closely packed and linearly-extended isophthalic acid units that realized the both efficient C2 and C3 paraffin preferential adsorption, respectively. The findings reveal an effective strategy to improve the affinity between paraffins and the frameworks through the construction of the periodically expanded and parallel-aligned aromatic-based units along the channel. Our developed material could produce ultra-high purity (99.99%) olefins, and the excellent paraffin/olefin separation selectivity and olefin productivity also well demonstrate the superiority of the strategy. This work not only presents a new benchmark porous material for paraffin/olefin separation, but will facilitate the future design of novel paraffin-selective materials for energy-efficient separations.

All reagents were analytical grade and used as received without further purification. Co(NO3)2·6H2O, Isophthalic acid (IPA), methanol (MeOH), and dimethylformamide (DMF) were purchased from Aladdin Reagent Co. Ltd., Meso-α,β-Di(4-pyridyl) Glycol (DPG) was purchased from TCI Co. Ltd. Ultra-high purity grade He (99.999%), N2 (99.999%), C2H4 (99.99%), C2H6 (99.99%), C3H6 (99.99%), C3H8 (99.99%), CO2 (99.999%), and mixed gases (C2H4/C2H6 = 50/50, v/v, C2H4/C2H6 = 15/1, v/v, C3H6/C3H8 = 50/50 v/v, C3H6/C3H8 = 95/5 v/v) were purchased from Shanghai Wetry Standard gas Co., Ltd. (China) and used for all measurements.

PCP-IPA was synthesized according to the previously reported procedure51. 81 mg DPG was dissolved in DMF/MeOH (1:1, 30 mL) at 60 °C, and 62 mg IPA and 109 mg Co(NO3)2·6H2O was dissolved in 5 mL MeOH. Then the two solutions were mixed and heated at 80 °C for 24 h hours to yield as-synthesized of PCP-IPA.

Powder X-ray diffraction (XRD) patterns were collected using a PANalytical empyrean series2 diffractometer with Cu-Ka radiation, at room temperature, with a step size of 0.0167°, a scan time of 15 s per step, and 2θ ranging from 5 to 50°. The morphology was investigated using a NOVA 200 Nanolab scanning electron microscope (SEM). Fourier transform infrared (FTIR) spectra was recorded in the range of 400–4000 cm−1 on a Nicolet 5700 FTIR spectrometer using KBr pellets. The thermogravimetric analysis (TGA) data were collected in a NETZSCH Thermogravimetric Analyzer (STA2500) from 25 to 700 °C with a heating rate of 10 °C/min. The CO2 adsorption/desorption isotherms at 195 K were obtained on a Micromeritics ASAP 2460 volumetric adsorption apparatus. The apparent Langmuir-specific surface area was calculated using the adsorption branch with the relative pressure P/P0 in the range of 0.005 to 0.1. The total pore volume (Vtot) was calculated based on the adsorbed amount of CO2 at the P/P0 of 0.99. The pore size distribution (PSD) was calculated using the H-K methodology with CO2 adsorption isotherm data and assuming a slit pore model.

The C2H4, C2H6, C3H6, and C3H8 adsorption–desorption isotherms at different temperatures were measured volumetrically by the Micromeritics ASAP 2460 adsorption apparatus for pressures up to 1.0 bar. The time-dependent gas uptake profiles of C2H4, C2H6, C3H6, and C3H8 were measured by Intelligent gravimetric adsorption (IGA-100, Hiden). Prior to the adsorption measurements, the samples were degassed using a high vacuum pump (<5 μm Hg) at 373 K for over 12 h.

The breakthrough experiments were carried out in a home-made apparatus. The sample was dried under vacuum at 100 °C for 12 h. Samples (about 1.29 g) were then introduced to the adsorption bed (φ6 mm × 150 mm). A carrier gas (He ≥99.999%) was used to purge the adsorption bed for more than 1 h to ensure that the adsorption bed was saturated with He. Then the gas flow is switched to the desired gas mixture without any inert gas dilution (C2H4/C2H6 = 50/50, v/v, C2H4/C2H6 = 15/1, v/v, C3H6/C3H8 = 50/50 v/v, C3H6/C3H8 = 95/5 v/v) at a certain flow rate. The recovery gas was passed to an analyzer port and analyzed using gas chromatography (GC490 Agilent) with a thermal conductivity detector (TCD). After breakthrough experiment, the adsorption column was regenerated at 100 °C with the 10 mL/min N2 flow rate for 2 h.

The pure-component isotherms of C2H6, C2H4, C3H8, and C3H6 were fitted using single-site Langmuir-Freundlich model for full range of pressure (0–1.0 bar).

here, p is the pressure of the bulk gas at equilibrium with the adsorbed phase (bar), q is the adsorbed amount per mass of adsorbent (mmol g−1), qsat is the saturation capacities (mmol g−1), b is the affinity coefficient (bar−1), and v represent the deviation from an ideal homogeneous surface.

The isosteric heat of C2H4, C2H6, C3H6, and C3H8 adsorption, Qst, defined as

were determined using the pure component isotherm fits using the Clausius-Clapeyron equation. where Qst (kJ/mol) is the isosteric heat of adsorption, T (K) is the temperature, P (bar) is the pressure, R is the gas constant, and q (mmol/g) is the adsorbed amount.

The selectivity of the preferential adsorption of component 1 over component 2 in a mixture containing 1 and 2 can be formally defined as:

In the above equation, x1 and y1 (x2 and y2) are the molar fractions of component 1 (component 2) in the adsorbed and bulk phases, respectively. We calculated the values of x1 and x2 using the ideal adsorbed solution theory (IAST) of Myers and Prausnitz56.

This separation potential, △Q, represents the maximum number of moles of pure component 2 (the less strongly adsorbed species) that can be recovered in the gas phase per gram of adsorbent in the fixed bed. The separation potential of adsorbers in fixed bed for paraffin/olefin separation is defined by57

where q1 and q2 are the molar loadings for mixture adsorption, calculated from the IAST in mmol/g, y2 and y1 are molar fractions in the binary mixture gas.

First-principles density functional theory (DFT) calculations were performed using the Materials Studio's CASTEP code58. All calculations were conducted under the generalized gradient approximation (GGA) with Perdew−Burke–Ernzerhof (PBE). A semiempirical addition of dispersive forces to conventional DFT was included in the calculation to account for van der Waals interactions. Cutoff energy of 544 eV and a 2 × 2 × 2 k-point mesh was found to be enough for the total energy to coverage within 0.01 meV atom−1. The structures of the synthesized materials were first optimized from the reported crystal structures. To obtain the binding energy, the pristine structure and an isolated gas molecule placed in a supercell (with the same cell dimensions as the pristine crystal structure) were optimized and relaxed as references. C2H4, C2H4, C3H6, and C3H8 gas molecules were then introduced to different locations of the channel pore, followed by a full structural relaxation. The static binding energy was calculated by the equation:

All data supporting the findings of this study are available within this article and its Supplementary Information. Source data that support the findings of this study are available from the corresponding author upon reasonable request. Correspondence and requests for materials should be addressed to H.X.

Sholl, D. S. & Lively, R. P. Seven chemical separations to change the world. Nature 532, 435–437 (2016).

Article ADS PubMed Google Scholar

Lin, J. Y. Molecular sieves for gas separation. Science 353, 121–122 (2016).

Article ADS CAS PubMed Google Scholar

Wu, Y. & Weckhuysen, B. M. Separation and purification of hydrocarbons with porous materials. Angew. Chem. Int. Ed. 60, 18930–18949 (2021).

Article CAS Google Scholar

Adil, K. et al. Gas/vapour separation using ultra-microporous metal–organic frameworks: insights into the structure/separation relationship. Chem. Soc. Rev. 46, 3402–3430 (2017).

Article CAS PubMed Google Scholar

Yang, L. et al. Energy-efficient separation alternatives: metal–organic frameworks and membranes for hydrocarbon separation. Chem. Soc. Rev. 49, 5359–5406 (2020).

Article CAS PubMed Google Scholar

Liao, P.-Q. et al. Controlling guest conformation for efficient purification of butadiene. Science 356, 1193–1196 (2017).

Article CAS PubMed Google Scholar

Wang, J. et al. Fine pore engineering in a series of isoreticular metal-organic frameworks for efficient C2H2/CO2 separation. Nat. Commun. 13, 1–8 (2022).

ADS Google Scholar

Hao, H. G. et al. Simultaneous trapping of C2H2 and C2H6 from a ternary mixture of C2H2/C2H4/C2H6 in a robust metal–organic framework for the purification of C2H4. Angew. Chem. Int. Ed. 130, 16299–16303 (2018).

Article ADS Google Scholar

Wang, H. et al. Topologically guided tuning of Zr-MOF pore structures for highly selective separation of C6 alkane isomers. Nat. Commun. 9, 1–11 (2018).

ADS CAS Google Scholar

Shen, J. et al. Simultaneous interlayer and intralayer space control in two-dimensional metal−organic frameworks for acetylene/ethylene separation. Nat. Commun. 11, 1–10 (2020).

Article CAS Google Scholar

Jiang, H. et al. A reticular chemistry guide for the design of periodic solids. Nat. Rev. Mater. 6, 466–487 (2021).

Article ADS CAS Google Scholar

Behera, N. et al. The chemistry and applications of flexible porous coordination polymers. EnergyChem 3, 100067 (2021).

Article CAS Google Scholar

Yaghi, O.M. et al. Introduction to Reticular Chemistry: Metal-organic Frameworks and Covalent Organic Frameworks (John Wiley & Sons, 2019).

Zhang, Z. et al. Optimal pore chemistry in an ultramicroporous metal–organic framework for benchmark inverse CO2/C2H2 separation. Angew. Chem. Int. Ed. 60, 17198–17204 (2021).

Article CAS Google Scholar

Li, J. et al. Purification of propylene and ethylene by a robust metal–organic framework mediated by host–guest interactions. Angew. Chem. Int. Ed. 60, 15541–15547 (2021).

Article CAS Google Scholar

Bereciartua, P. J. et al. Control of zeolite framework flexibility and pore topology for separation of ethane and ethylene. Science 358, 1068–1071 (2017).

Article ADS CAS PubMed Google Scholar

Lin, R.-B. et al. Molecular sieving of ethylene from ethane using a rigid metal–organic framework. Nat. Mater. 17, 1128–1133 (2018).

Article ADS CAS PubMed Google Scholar

Bao, Z. et al. Molecular sieving of ethane from ethylene through the molecular cross‐section size differentiation in gallate‐based metal–organic frameworks. Angew. Chem. Int. Ed. 130, 16252–16257 (2018).

Article ADS Google Scholar

Ding, Q. et al. Exploiting equilibrium-kinetic synergetic effect for separation of ethylene and ethane in a microporous metal-organic framework. Sci. Adv. 6, eaaz4322 (2020).

Article ADS CAS PubMed PubMed Central Google Scholar

Zeng, H. et al. Orthogonal-array dynamic molecular sieving of propylene/propane mixtures. Nature 595, 542–548 (2021).

Article ADS CAS PubMed Google Scholar

Yu, L. et al. Pore distortion in a metal–organic framework for regulated separation of propane and propylene. J. Am. Chem. Soc. 143, 19300–19305 (2021).

Article CAS PubMed Google Scholar

Wang, Y. et al. Selective aerobic oxidation of a metal–organic framework boosts thermodynamic and kinetic propylene/propane selectivity. Angew. Chem. Int. Ed. 131, 7774–7778 (2019).

Article ADS Google Scholar

Yu, M.-H. et al. Enhanced gas uptake in a microporous metal–organic framework via a sorbate induced-fit mechanism. J. Am. Chem. Soc. 141, 17703–17712 (2019).

Article CAS PubMed PubMed Central Google Scholar

Lyndon, R. et al. Tuning the structures of metal–organic frameworks via a mixed-linker strategy for ethylene/ethane kinetic separation. Chem. Mater. 32, 3715–3722 (2020).

Article CAS Google Scholar

Cadiau, A. et al. A metal-organic framework–based splitter for separating propylene from propane. Science 353, 137–140 (2016).

Article ADS CAS PubMed Google Scholar

Wang, H. et al. Tailor‐made microporous metal–organic frameworks for the full separation of propane from propylene through selective size exclusion. Adv. Mater. 30, 1805088 (2018).

Article CAS Google Scholar

Cao, J.-W. et al. One-step ethylene production from a four-component gas mixture by a single physisorbent. Nat. Commun. 12, 1–8 (2021).

Article ADS CAS Google Scholar

Chen, K.-J. et al. Synergistic sorbent separation for one-step ethylene purification from a four-component mixture. Science 366, 241–246 (2019).

Article ADS CAS PubMed Google Scholar

Liang, B. et al. An ultramicroporous metal–organic framework for high sieving separation of propylene from propane. J. Am. Chem. Soc. 142, 17795–17801 (2020).

Article CAS PubMed Google Scholar

Yang, H. et al. Pore-space-partition-enabled exceptional ethane uptake and ethane-selective ethane–ethylene separation. J. Am. Chem. Soc. 142, 2222–2227 (2020).

Article CAS PubMed Google Scholar

Hartmann, M. et al. Adsorptive separation of olefin/paraffin mixtures with ZIF-4. Langmuir 31, 12382–12389 (2015).

Article CAS PubMed Google Scholar

Pires, J. et al. Ethane selective IRMOF-8 and its significance in ethane–ethylene separation by adsorption. ACS Appl. Mater. Interfaces 6, 12093–12099 (2014).

Article CAS PubMed Google Scholar

Gucuyener, C. et al. Ethane/ethene separation turned on its head: selective ethane adsorption on the metal−organic framework ZIF-7 through a gate-opening mechanism. J. Am. Chem. Soc. 132, 17704–17706 (2010).

Article PubMed CAS Google Scholar

Pascual, P. et al. Development of a transferable guest-host force field for adsorption of hydrocarbons in zeolites. II. Prediction of alkenes adsorption and alkane/alkene selectivity in silicalite. J. Phys. Chem. B 108, 393–398 (2004).

Article CAS Google Scholar

Li, L. et al. Ethane/ethylene separation in a metal-organic framework with iron-peroxo sites. Science 362, 443–446 (2018).

Article ADS CAS PubMed Google Scholar

Liao, P.-Q. et al. Efficient purification of ethene by an ethane-trapping metal-organic framework. Nat. Commun. 6, 1–9 (2015).

Article ADS CAS Google Scholar

Zeng, H. et al. Cage-interconnected metal–organic framework with tailored apertures for efficient C2H6/C2H4 separation under humid conditions. J. Am. Chem. Soc. 141, 20390–20396 (2019).

Article CAS PubMed Google Scholar

Geng, S. et al. Scalable room-temperature synthesis of highly robust ethane-selective metal–organic frameworks for efficient ethylene purification. J. Am. Chem. Soc. 143, 8654–8660 (2021).

Article CAS PubMed Google Scholar

Chen, C. X. et al. Nanospace engineering of metal–organic frameworks through dynamic spacer installation of multifunctionalities for efficient separation of ethane from ethane/ethylene mixtures. Angew. Chem. Int. Ed. 60, 9680–9685 (2021).

Article ADS CAS Google Scholar

He, C. et al. Modification of the pore environment in UiO-type metal-organic framework toward boosting the separation of propane/propylene. Chem. Eng. J. 403, 126428 (2021).

Article CAS Google Scholar

Chen, Y. et al. An ethane-trapping MOF PCN-250 for highly selective adsorption of ethane over ethylene. Chem. Eng. Sci. 175, 110–117 (2018).

Article CAS Google Scholar

Lin, R.-B. et al. Boosting ethane/ethylene separation within isoreticular ultramicroporous metal–organic frameworks. J. Am. Chem. Soc. 140, 12940–12946 (2018).

Article CAS PubMed Google Scholar

Zhang, X. et al. Selective ethane/ethylene separation in a robust microporous hydrogen-bonded organic framework. J. Am. Chem. Soc. 142, 633–640 (2019).

Article PubMed CAS Google Scholar

Zhang, X. et al. A rod‐packing hydrogen‐bonded organic framework with suitable pore confinement for benchmark ethane/ethylene separation. Angew. Chem. Int. Ed. 133, 10392–10398 (2021).

Article ADS Google Scholar

Qazvini, O. T. et al. A robust ethane-trapping metal–organic framework with a high capacity for ethylene purification. J. Am. Chem. Soc. 141, 5014–5020 (2019).

Article CAS PubMed Google Scholar

Su, K. et al. Efficient ethylene purification by a robust ethane-trapping porous organic cage. Nat. Commun. 12, 1–7 (2021).

Article ADS CAS Google Scholar

Xu, Z. et al. A robust Th-azole framework for highly efficient purification of C2H4 from a C2H4/C2H2/C2H6 mixture. Nat. Commun. 11, 1–9 (2020).

ADS CAS Google Scholar

Yang, L. et al. Polycatenated molecular cage-based propane trap for propylene purification with recorded selectivity. ACS Appl. Mater. Interfaces 12, 2525–2530 (2019).

Article CAS PubMed Google Scholar

Hong, A. N. et al. Pore-space partition and optimization for propane-selective high-performance propane/propylene separation. ACS Appl. Mater. Interfaces 13, 52160–52166 (2021).

Article CAS Google Scholar

Yang, S.-Q. et al. Propane-trapping ultramicroporous metal–organic framework in the low-pressure area toward the purification of propylene. ACS Appl. Mater. Interfaces 13, 35990–35996 (2021).

Article CAS PubMed Google Scholar

Gu, Y. et al. Host–guest interaction modulation in porous coordination polymers for inverse selective CO2/C2H2 separation. Angew. Chem. Int. Ed. 60, 11688–11694 (2021).

Article CAS Google Scholar

Pei, J. et al. Engineering microporous ethane-trapping metal–organic frameworks for boosting ethane/ethylene separation. J. Mater. Chem. A 8, 3613–3620 (2020).

Article CAS Google Scholar

Kang, M. et al. A robust hydrogen-bonded metal–organic framework with enhanced ethane uptake and selectivity. Chem. Mater. 33, 6193–6199 (2021).

Article CAS Google Scholar

Peng, J. et al. Selectively trapping ethane from ethylene on metal–organic framework MIL-53 (Al)-FA. Ind. Eng. Chem. Res. 58, 8290–8295 (2019).

Article CAS Google Scholar

Kang, M. et al. High‐throughput discovery of Ni (IN) 2 for ethane/ethylene separation. Adv. Sci. 8, 2004940 (2021).

Article CAS Google Scholar

Myers, A. L. & Prausnitz, J. M. Thermodynamics of mixed‐gas adsorption. AIChE J. 11, 121–127 (1965).

Article CAS Google Scholar

Krishna, R. Methodologies for screening and selection of crystalline microporous materials in mixture separations. Sep. Purif. Technol. 194, 281–300 (2018).

Article CAS Google Scholar

Segall, M. et al. First-principles simulation: ideas, illustrations and the CASTEP code. J. Phys. Condens. Mat. 14, 2717 (2002).

Article ADS CAS Google Scholar

Download references

This work is supported by the Zhejiang Provincial Natural Science Foundation of China (No. LR20B060001), the National Natural Science Foundation of China (No. 22108240, 21725603, and 21938011), and the Research Computing Center in College of Chemical and Biological Engineering at Zhejiang University.

Key Laboratory of Biomass Chemical Engineering of Ministry of Education, College of Chemical and Biological Engineering, Zhejiang University, Hangzhou, 310027, Zhejiang, P. R. China

Peixin Zhang, Lifeng Yang, Liyuan Chen, Xili Cui & Huabin Xing

ZJU-Hangzhou Global Scientific and Technological Innovation Center, Hangzhou, 311215, Zhejiang, P. R. China

Peixin Zhang, Xian Suo, Xili Cui & Huabin Xing

Chemistry and Chemical Engineering School, Nanchang University, Nanchang, 330031, Jiangxi, P. R. China

Xing Liu & Jun Wang

You can also search for this author in PubMed Google Scholar

H.X., L.Y., X.C., and P.Z. conceived the project idea, designed the research, and co-wrote the manuscript. P.Z. carried out the materials synthesis, adsorption experiments, transient breakthrough measurements, and computational simulation. X.S. conducted the cycling breakthrough experiment. L.C. performed the IAST calculation. J.W. and X.L. contributed to the measurement of time-dependent gas uptake profiles. All authors contributed to the discussion of results and commented on the manuscript.

Correspondence to Huabin Xing.

The authors declare no competing interests.

Nature Communications thanks Martin Hartmann, Banglin Chen and the other, anonymous, reviewer for their contribution to the peer review of this work.

Publisher's note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and Permissions

Zhang, P., Yang, L., Liu, X. et al. Ultramicroporous material based parallel and extended paraffin nano-trap for benchmark olefin purification. Nat Commun 13, 4928 (2022). https://doi.org/10.1038/s41467-022-32677-3

Download citation

Received: 16 March 2022

Accepted: 11 August 2022

Published: 22 August 2022

DOI: https://doi.org/10.1038/s41467-022-32677-3

Anyone you share the following link with will be able to read this content:

Sorry, a shareable link is not currently available for this article.

Provided by the Springer Nature SharedIt content-sharing initiative

Nature Communications (2023)

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.