Ion-Exchanged ZIF-67 Synthesized by One-Step Method for Enhancement of CO<sub>2</sub> Adsorption

Song, Fujiao; Cao, Yan; Zhao, Yunxia; Jiang, Ruiyu; Xu, Qi; Yan, Jinlong; Zhong, Qin

doi:https://doi.org/10.1155/2020/1508574

Journal of Nanomaterials

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Abstract Introduction Materials and Methods Results and Discussion Conclusions Data Availability Disclosure Conflicts of Interest Authors’ Contributions Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2020 | Article ID 1508574 | https://doi.org/10.1155/2020/1508574

Ion-Exchanged ZIF-67 Synthesized by One-Step Method for Enhancement of CO₂ Adsorption

Fujiao Song,¹Yan Cao,¹Yunxia Zhao,²Ruiyu Jiang,³Qi Xu,¹Jinlong Yan,¹and Qin Zhong⁴

Academic Editor: Dong Kee Yi

Received15 Oct 2019

Accepted04 Dec 2019

Published17 Feb 2020

Abstract

Li⁺- and Na⁺-exchanged ZIF-67 was synthesized by a new one-step method of ion as-exchange technique and tested as CO₂ adsorbents. As a comparison, the standard ion-exchange procedure was also carried out. The powder X-ray diffraction (XRD), scanning electronic microscope (SEM), particle size analyzer (PSD), and thermal gravimetry analysis (TGA) were used to investigate the effect of ion-exchange techniques on the structure of the materials. CO₂ uptake of ZIF-67 ion exchanged by one-step method is much higher than that by the standard ion-exchange procedure. All of the adsorption isotherms show linear patterns with stable adsorption rate from 0 bar to 1 bar, which reveals the materials could get excellent adsorption performance at higher pressure range (>1 bar). Elemental analysis, N₂ physical adsorption, and the point of zero charge (PZC) were carried out to confirm the adsorption mechanism. van der Waals interaction determined by the surface area and coordination interaction resulting from electrostatic interaction work in synergy to enhance CO₂ adsorption performance of ZIF-67 ion exchanged by the one-step method.

1. Introduction

Zeolitic imidazolate frameworks (ZIFs) are a new class of porous materials constructed from coordinated divalent cations (e.g., Zn, Co) linked by imidazolate (Im) [1]. Many ZIFs have unusual high thermal and chemical stability for metalorganic frameworks [2, 3]. The well-known ZIF-8 is a prime example with a sodalite (SOD) topology, which can be boiled in water and other solvents without damage of the structure [4]. ZIF-67 is isostructural to ZIF-8 and is formed by linking 2-methylimidazolate anions and cobalt cations [5].

ZIFs have shown great potential applications in gas separation [6–8] and catalysis [9–11] because of their tunable zeotype topologies, high surface area, and metal content. To obtain ZIF adsorbents with large surface areas, adjustable pore sizes, open metal sites, and excellent CO₂ adsorption property, various functionalization techniques have been applied, such as functionalization with amine groups [12], specific functionalization of the imidazolate [13], isoreticular covalent functionalization [14, 15], formation of ZIF-inorganic substance composites [16], and cation exchange [17]. Among these functionalization methods, ion exchange could improve the surface area, pore volume, and surface charge of the adsorbents, further enhancing the CO₂ adsorption capacities. Lan et al. [18] found that Li was the best exchangeable cation of covalent organic frameworks (COFs) for CO₂ adsorption among alkali metal, alkaline-earth metal, and transition metal by the multiscale simulation approach.

A standard ion-exchange procedure was carried out as follows [19, 20]: the dried as-prepared sample was suspended in a 0.1 M sodium nitrate solution using an ethanol-water mixture of molar ratio 3 : 1 and stirred at room temperature for 24 h. Obviously, the standard ion-exchange procedure could attributed to postsynthesis modification. And CO₂ uptake properties of the sorbents could be enhanced significantly [21, 22]. However, it is notable that the standard ion-exchange process needs to be repeated for several times, which brings a series of disadvantages, such as complicated in synthesis, time consuming, and solvent consuming.

In this work, we develop a new one-step ion-exchange method (donated as ion as-exchange technique) to overcome the disadvantages mentioned above. Since the cations for exchange were added before the hydrothermal preparation of ZIF-67, time consuming and solvent consuming in the standard ion-exchange procedure were eliminated. By comparison, the standard ion-exchange procedure was also carried out to synthesize the adsorbents. The structure, surface charge, and CO₂ adsorption properties of the adsorbents prepared via the two methods were investigated and compared.

2. Materials and Methods

2.1. Materials

All chemicals were analytic grade provided by Aladdin Chemical Reagent Co., Ltd., Shanghai, China.

2.2. Synthesis of the ZIF-67 and Ion-Exchanged ZIF-67

ZIF-67 was synthesized with the following procedure [23]. A solid mixture of Co(NO₃)₂·6H₂O (2.91 g, 10 mmol) and 2-methylimidazole (4.105 g, 50 mmol) was dissolved in methanol (150 ml) in a 200 ml Teflon liner with stirring. The Teflon liner was sealed with an autoclave and heated at 140°C for 72 h in a convection oven. After the product was cooled naturally to room temperature, chloroform was added to the product, and the crystals were collected from the upper layer. The crystals were immersed in methanol for 3 days and the solvent was exchanged with a fresh solvent daily.

The synthesis of ion-exchanged ZIF-67 was performed with ion as-exchange technique and ion post-exchanged technique (standard ion-exchange procedure).

Lithium nitrate (LiNO₃) or sodium nitrate (NaNO₃) was dissolved in the solutions containing Co(NO₃)₂·6H₂O and 2-methylimidazole. The synthesis and activation of ion as-exchanged ZIF-67 followed the same route of ZIF-67. The dark blue product was designated as M-as- (mole ratio of M : ), where M represents the alkali metal ions (Li and Na); represents the mole ratio of Li : Co (, 5 and 25).

In the synthesis of ion post-exchanged ZIF-67, dried as-prepared ZIF-67 was ion-exchanged with Li⁺ and Na⁺ cations. For this purpose, the as-prepared ZIF-67 was immersed in a solution of lithium and sodium chlorides in pure freshly distilled methanol, and stirred at room temperature for 24 h. The ion-exchange process was repeated 4 times. The dark blue product was obtained by filtration and drying, designated as M-post-5, where M represents the alkali metal ion (Li and Na); 5 represents the mole ratio of M : Co.

2.3. Characterization and Adsorption Measurements

The powder X-ray diffraction (XRD) (Beijing Purkinje General Instrument Co., Ltd., China) patterns were recorded using nickel-filtered Cu Kα radiation at 36 kV and 40 mA (2θ ranging from 5° to 80°, and 0.02° step size). The morphologies and composition of samples were observed on the Hitachi-S4800 FESEM (Hitachi Electronics Co., Ltd., Japan) at an acceleration voltage of 30 kV. EDS mapping was applied to analyze the element extent and locate the elemental distribution on the surface of the materials. Metallic element (Co, Li and Na) was measured by OPTIMA 5300DV inductive-coupled plasma emission spectrometer (ICP-AES) (PerkinElmer Co. Ltd., Japan). The particle size distribution of the samples was measured using BT-9300S Laser Particle Size Analyzer (Dandong Bettersize Instrument Ltd., China) using water as dispersion medium. TG and DTG curves were obtained under oxygen atmosphere by Pyris 1 TGA heating from 30°C to 800°C at 20.00°C/min.

CO₂ adsorption isotherms were measured using a surface area and pore porosimetry analyzer (V-Sorb 2800P) under low pressure (0-1.1 bar). The experiments were conducted at 0°C by the Dewar flask using ice water or circulated water in which the sample tube was immersed. Prior to each adsorption experiment, the samples were degassed at 120°C overnight. N₂ adsorption isotherms were measured using an ASAP 2020 analyzer (Micromeritics, Norcross, GA, USA) under low pressure (0-1.1 bar). The experiments were conducted at 0°C and 25°C. The reversibility of the CO₂ adsorption process on the samples studied was tested by multiple CO₂ adsorption cycles. The corresponding adsorption isotherms have been acquired after heating at 120°C for 12 h in vacuum in sequence.

The BET surface areas () and pore volumes () of given samples were determined by surface area and pore porosimetry analyzer (V-Sorb 2008P). The point of zero charge (pH_PZC) for the parent ZIF-67 and ion-exchanged ZIF-67 was estimated by a mass titration method [24]. After adsorption of CO₂ in the surface area analyzer mentioned above, pH_PZC of the adsorbents was measured with the same method.

3. Results and Discussion

Figure 1 shows the XRD patterns of ZIF-67 exchanged with Li⁺ and Na⁺ Figure 1(a) and that exchanged with different concentrations of Li⁺ Figure 1(b). The diffraction pattern of parent ZIF-67 is in accordance with the data in the reported literature, indicating that the product was pure-phase ZIF-67 materials [25]. As shown in Figure 1(a), all the Li⁺- and Na⁺-exchanged ZIF-67 maintain crystallinity of the original phase. And almost no changes in peak intensity and position could be observed. Figure 1(b) reveals that the different Li⁺-exchanged concentrations have no effect either on the crystallinity.

(a)

(b)

Figure 2 shows the scanning electron microscopy (SEM) images and EDX mapping of the parent and ion-exchanged ZIF-67 materials. As revealed in Figure 2(a1), the crystals of parent ZIFs are comprised of mostly regular multifaceted crystals with sharp edges and smooth surface [26]. The particle size is similar and around 300 nm. Ion-exchanged ZIF-67 remains in the original polyhedral shape in various degrees. Most dramatically, Li⁺- and Na⁺-post-exchanged ZIFs (Figures 2(b1) and 2(c1)) tend to clump and agglomerate with smaller irregular polyhedral and tough surface because of the physical operations during the ion-post-exchanged procedure, such as stirring, while the as-exchanged samples (Figures 2(d1), 2(e1), 2(f), and 2(g)) maintain good dispersion and polyhedral shape. A change of the crystal sizes could be also observed. Na⁺ as-exchanged ZIFs show an increase in the crystal size, while other ion-exchanged ZIFs show the decrease in crystal size with varying degrees. In addition, the particle sizes of Li⁺ as-exchanged ZIFs decrease with the increase of ratio of Li⁺ : Co²⁺. Furthermore, the ZIF-67-Li-as-25 displayed the minimum crystal size, which is 200 nm approximately.

EDX mapping of parent ZIF-67 indicates that all C, N, and Co elements are dispersed uniformly on the surface of the materials. Similar situations occur in the EDX mapping of Co and Na for other ion-exchanged ZIFs, revealing that ion exchange may arise on the surface of the crystals evenly or randomly. The colour of Na element in Figure 2(c2) is much darker than that in Figure 2(e2), which probably proves that the Na content on the surface of Na-post-5 is higher than that of Na-as. Moreover, Li element is unable to be measured by EDX mapping since it is beyond the scope of the test method.

Element content of metallic element (Co, Li, and Na) on the surface and all over the material was measured by SEM-EDX and ICP-AES, respectively. As listed in Table 1, the Co content (wt%) of all the samples measured by EDX is much less than that by ICP, whereas the Na content test exhibits the opposite result. It indicates that the Co content on the surface of the crystals is less than its actual content. The ion exchange mainly occurred on the surface of the crystals. After the conversion of wt% to mol%, ICP result reveals that the mole ratios of M (Li or Na) : (M and Co) in M-as-5 are 17.89% and 15.91%, whereas that in M-post-5 are 32.19% and 31.72%. Most dramatically, M content in M-post is much higher than the content of reduced Co compared to the parent ZIF-67. Therefore, some M ions may physically deposit on the surface of the crystals rather than exchanging with Co ions.

Figure 3 presents the particle size distributions of as-synthesized and ion-exchanged ZIF-67 samples, which show the Gaussian-type distribution. The as-synthesized ZIF-67 crystals have an average particle size of 317 nm. After ion as-exchanged treatment, the average particle sizes of Li/Na-as-5 changed to 256 nm and 339 nm, respectively, which matches well with the trend of SEM observations (Figure 2). Dramatically, the particle size distributions of Li/Na-post-5 became broader, and the average particle sizes increased to 336 nm and 342 nm, respectively, which was in contrast with the trend of SEM results. It can be attributed to the agglomerate phenomenon observed from Figure 2. As seen from Figure 3(b), the average particle sizes of Li-as-1/5/25 were 289 nm, 256 nm, and 213 nm, respectively, decreasing with the increase of ratio of Li⁺ : Co²⁺.

(a)

(b)

3.1. Adsorption Studies

The corresponding CO₂ adsorption isotherms of parent and these ion-exchanged ZIFs are shown in Figure 4(a). At 0°C, the CO₂ uptake of parent ZIF-67 at 1 bar is 35.4 cm³/g. Li/Na-post-5 exhibited decreased CO₂ adsorption capacity (30.4 and 31.2 cm³/g) compared to the parent, while Li/Na-as-5 showed improved CO₂ uptake values (48.7 and 45.1 cm³/g). The highest CO₂ capacity is achieved by Li-as-5, which is 37.6% higher than that of the parent ZIF-67. At 250°C, the CO₂ uptakes on ZIF samples follow the similar order. The decreases in adsorption amount of post-exchanged ZIFs were correlated with the clump and agglomerate (Figures 2(b) and 2(c)). This phenomenon may lead to a decrease in pore volume and adsorption sites, which was extremely similar to the effect of carbon deposition behavior on pore volume [27, 28]. In Figure 4(b), the CO₂ uptake of Li-as- with varying Li⁺ : Co²⁺ ratios at 1 bar was 41.8, 48.7, and 37.6 cm³/g, respectively, which could not be directly correlated with the amounts of Li⁺. An interesting phenomenon is found that all of the isotherms show linear patterns with stable adsorption rate from 0 bar to 1 bar, which could be attributed to monomolecular adsorption (Henry-type model). It reveals the materials could get excellent adsorption performance at higher pressure range (>1 bar).

(a)

(b)

(c)

(d)

The CO₂/N₂ adsorption isotherms of parent ZIF-67, Li-post-5, and Li-as-5 are collected in Figure 4(c) to calculate the CO₂/N₂ selectivity. The N₂ uptakes of the 3 samples follow the order of their CO₂ uptake. The corresponding linear fit results are also shown in Figure 4(c). The CO₂/N₂ selectivity could be calculated by the ratio of Henry coefficient, which is equal to the slope of the isotherms after linear fit. Therefore, S (CO₂/N₂) of parent ZIF-67, Li-post-5, and Li-as-5 is 18.21, 18.27, and 19.02, respectively, showing a good selectivity for CO₂/N₂ separation.

The interaction of guest molecules with host materials is usually evaluated by the isosteric heat of adsorption [29, 30]. Figure 4(d) shows that the on ZIF-67 for CO₂ follows the following order: Li-as > Na-as > Li-post > Na-post > parent, which was different from the order of their CO₂ uptakes. It is suggested that the dispersion of the Li and Na species can create a high electric field on the surface of ZIF, leading to a higher binding force with quadrupolar CO₂ molecules [31].

3.2. CO₂ Adsorption Mechanism

To confirm the reason for varying CO₂ adsorption capacities of ion-exchanged ZIFs, low temperature N₂ adsorption and PZC characterization were carried out.

N₂ adsorption isotherms and pore size distributions of the parent and ion-exchanged ZIF-67 materials are shown in Figure 5. Physical properties of these materials are listed in Table 2 and Table 3. As revealed in Figure 5(a), the isotherm of parent ZIF-67 reveals typical type I behavior as expected for microporous materials, corresponding to that reported in the literatures [32, 33]. The surface area, pore volume, and SF median pore width are 1424.59 m²/g, 0.84 cm³/g, and 0.868 nm, respectively. As shown in Figure 5(b), the pore size of parent ZIF-67 was distributed at 0.86, 1.18, and 1.36 nm.

(a)

(b)

(c)

(d)

The entire ion-exchanged ZIFs maintained type I isotherms and similar pore size distribution with a right shift, while the pore volumes of Li/Na-post-5 decreased dramatically. As shown in Table 2, the surface area, pore volume, and SF median pore width of Li/Na-as-5 increase significantly, while those of post-exchanged materials decrease contrarily. It was reported that the standard ion-exchange procedure could improve the surface area and pore volume [34], which was opposite to our results. As can be seen from Figure 5(b), although the second pore size distribution peak of Li/Na-post-5 shifts from 1.18 nm to 1.21 nm and 1.20 nm, respectively, their peak height decreases significantly, indicating a decrease of pore volume. That is because the concentration of exchanged ions in our procedure is much higher than that in the standard ion-exchange procedure. A small quantity of Li⁺ or Na⁺ with smaller radius replaced Co²⁺ of ZIF-67, leading to an expanded pore size as mentioned above. However, other Li⁺/Na⁺ remained in the pores or attached on the surface, resulting in agglomerate and pore block.

The N₂ adsorption isotherms and pore size distribution of the parent and as-exchanged ZIF-67 with different concentrations of Li⁺ are collected in Figures 5(c) and 5(d). Their physical properties are listed in Table 3. The surface area and pore volume of Li-as-exchanged sample (Li⁺/) are 1450.71 cm²/g and 0.84 cm³/g, which is the highest value among all the samples. When the Li⁺ : Co²⁺ ratio increased to 25, surface area and pore volume declined to 1353.96 cm²/g and 0.71 cm³/g. Therefore, the Li⁺ ion as-exchange technique enhanced the surface area and pore volume to the greatest extent. And the optimal Li⁺ : Co²⁺ ratio is 5.

The position of the PZC defines the affinity of the surface of the adsorbents to the adsorbate. Therefore, determination of the PZC is an important element of the characterization of adsorbents [35]. In order to study the influence of ion-exchange procedures and exchanged ion species on the acid-base properties of the ZIF-67 surfaces, the point of zero charge (pH_PZC) was estimated by a mass titration method. The pH_PZC values of the parent ZIF-67 and ion-exchanged ZIF-67 before and after CO₂ adsorption are listed in Table 4 and Table 5.

As shown in Table 4, parent ZIF-67 has a neutral character with pH_PZC value of 6.92, whereas ion-exchanged ZIF_S have basic surfaces (pH_PZC values ranging from 7.51-9.26). Obviously, pH_PZC values of Li⁺ and Na⁺ as-exchanged ZIFs are higher than those of post-exchanged samples. And Li-as exhibits the highest pH_PZC value of 9.26, indicating that ion as-exchange technique with Li⁺ could enhance the surface basicity of the adsorbents to the greatest degree. The pH_PZC values of all samples decreased to the range of 5.10-5.63 after CO₂ adsorption. In Table 5, pH_PZC values of Li⁺ as-exchanged ZIFs increased with the increase of Li⁺ : Co2⁺ ratios. After CO₂ adsorption, pH_PZC decreased to the range of 5.14-5.42 similarly as before.

The mechanism of CO₂ adsorption on the parent and Li⁺/Na⁺ as-exchanged ZIF-67 is deduced in Figure 6. Because the radius of Li⁺ and Na⁺ was smaller than that of Co²⁺, the Li⁺/Na⁺ ion as-exchange technique enhanced the surface area and pore volume. Li⁺ has a smaller radius compared with Na⁺; thus, ZIF-67-Li-as shows the highest surface area and pore volume. As mentioned above, the order of CO₂ uptake of the samples is consistent with that of surface area. It confirmed that CO₂ adsorption on the synthesized adsorbents is dependent on van der Waals interaction determined by the surface area to a great degree.

According to the hard and soft acid-base principle (HASB principle), both Li⁺ and Na⁺ in ZIFs could be regarded as Lewis acid with strong attractive force on outer electrons. They could coordinate with CO₂ considered as a kind of Lewis base, which improved CO₂ adsorption. And the coordination interaction mainly results from electrostatic interaction [36]. Since Li⁺ has a larger radius to charge ratio compared with Na⁺, Li⁺ cation owns strong quadrupole moment (ΦFQ), further enhancing the strong affinity of Li⁺ ions for CO₂ molecules. According to Kumar et al.’s report [16], the CO₂ adsorption capacity in ion-exchanged sod-ZMOF appears to depend not only on the size and charge of the balancing cations but also on the distribution of the cations located in the framework structures, which is not exactly known at present. In short, van der Waals interaction determined by the surface area and coordination interaction resulting from electrostatic interaction work in synergy to enhance CO₂ adsorption. Although the adsorbent prepared via the post ion-exchange method contains more Li⁺/Na⁺ cations, the pore volumes decreased dramatically due to the agglomerate and pore block by excessive cations. Synergistic effects lead to worse CO₂ adsorption properties on Li-post and Na-post.

3.3. CO₂ Adsorption-Desorption Isotherms and Cyclic Adsorption-Regeneration Test

Figure 7(a) depicts the CO₂ adsorption-desorption isotherms of parent ZIF-67, Li-post-5, and Li-as-5 at 0°C. Dramatically, all of the 3 desorption isotherms lag behind the corresponding adsorption isotherms, with a small quantity of undesorbed CO₂ left in the adsorbents after the desorption process. Because the desorption isotherms were carried out from 1 bar to 0.05 bar, the adsorbed CO₂, undesorbed CO₂ at 0.05 bar, and other related parameters are listed in Table 6 to analyze the adsorption-desorption performance. The decrement of parent ZIF-67, Li-post-5, and Li-as-5 is 6.7%, 8.3%, and 7.6%, respectively, corresponding to the chemically adsorbed CO₂ by coordination interaction.

(a)

(b)

Figure 7(b) depicts the CO₂ adsorption-regeneration cycle of Li-as-5 in consideration of its optimal adsorption capacity. The regeneration was performed at 120°C in vacuum in sequence. The adsorption/regeneration cycle was repeated for a total of 4 cycles. And the cyclic CO₂ adsorption capacities of the 4 cycles at 1 bar are 47.3 cm³/g, 48.0 cm³/g, 47.7 cm³/g, and 46.9 cm³/g, respectively. The decrement of cyclic CO₂ adsorption after regeneration at 120°C in vacuum is in the range of 1.4%-3.7%. However, the decrement of CO₂ adsorption-desorption isotherms (desorbed at 0°C) is 7.6% as mentioned above. The former decrement was smaller than the latter decrement; that is to say, most of the undesorbed CO₂ of Li-as-5 at 0°C (chemically adsorbed CO₂ by coordination interaction) could be desorbed at 120°C in vacuum. It indicated that the CO₂ coordination adsorption on Li-as was weak and almost reversible at a higher temperature in vacuum, similar to the chemisorptions of CO₂ on amine-functionalized adsorbents [37, 38].

3.4. Thermal Stability Characterized by TGA

TG and DTG curves of ZIF-67 and Li-as-exchanged ZIF-67 with varying Li⁺ : Co²⁺ ratios are collected in Figure 8(a) and Figure 8(b), respectively. As shown in Figure 8(a), ZIF-67 shows that only 2.3% weight loss up to 350°C, corresponding to the removal of guest molecules and unreacted species [39]. Thus, the ZIF-67 material is thermally stable below 350°C at O₂ atmosphere. Although the thermal stability of ZIF-67 is slightly lower than that of ZIF-8 (ca. 500°C) [40], it still surpasses most of MOF materials [41]. The thermal stability of Li⁺ ion as-exchanged samples was improved in various degrees. The Li-as-exchanged materials with Li⁺ : Co²⁺ ratio of 5 and 25 enhanced its thermostability slightly, while that of Li⁺ : Co²⁺ ratio of 1 was improved dramatically, which could be thermally stable up to 390°C. Accordingly, a similar trend can be informed in the DTG curves of Figure 8(b). The weight loss rate of Li⁺ ion as-exchanged samples decreased in varying degrees and the weight loss peaks shifted to higher temperature, indicating that the Li⁺ ion as-exchange technique improved the thermal stability of ZIF-67 materials. In addition, it was observed that sharp turning points of unit decomposition in TG and DTG curves, as the curves were obtained under O₂ atmosphere, which accelerate the decomposition of the samples. When O₂ atmosphere was replaced by N₂ atmosphere, the turning points became smoother. Similar results were obtained by Chen et al.’s study [42].

(a)

(b)

4. Conclusions

Li⁺- and Na⁺-exchanged ZIF-67 was synthesized by a new one-step method of ion as-exchange technique for CO₂ capture. By comparison, the standard ion-exchange procedure of ion post-exchanged technique was also carried out. The structure, surface charge, and CO₂ adsorption properties and mechanism of the adsorbents prepared via the two methods were investigated. The surface area and pore volume of Li⁺/Na⁺ as-exchanged ZIF-67 increase significantly because the radius of Li⁺ and Na⁺ is smaller than that of Co²⁺. And the optimal Li⁺ : Co²⁺ ratio is 5. However, the surface area of post-exchanged materials decreases contrarily due to the agglomerate and pore block, which could be proved by SEM and particle size distribution results. PZC characterization indicates that parent ZIF-67 has a neutral character, whereas ion-exchanged ZIFs have basic surfaces. And pH_PZC values of Li⁺ and Na⁺ as-exchanged ZIFs are higher than those of post-exchanged samples, which could improve CO₂ adsorption due to the coordination interaction. All of the CO₂ adsorption isotherms show linear patterns with stable adsorption rate from 0 bar to 1 bar, which reveals the materials could get excellent adsorption performance at higher pressure range (>1 bar). van der Waals interaction determined by the surface area and coordination interaction resulting from electrostatic interaction work in synergy to enhance CO₂ adsorption performance of Li⁺/Na⁺ as-exchanged ZIF-67 adsorbents.

Data Availability

The data used to support the findings of this study are included within the article.

Disclosure

A conference abstract entitled “A one-step ion exchange method to functionalized ZiF-67 for enhanced CO₂ capture” has been presented in 2016 AIChE Annual Meeting in the following link: https://aiche.confex.com/aiche/2016/webprogram/Paper454249.html. The abstract only published the preliminary or partial results of scientific research without detailed results and discussion, and a large number of other data in this manuscript have not been published.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Authors’ Contributions

Dr. Qin Zhong has made a significant scientific contribution to the manuscript.

Acknowledgments

Specially, we would like to thank Dr. Qin Zhong from Nanjing University of Science and Technology for providing some testing instruments and revising the manuscript. In addition, we would like to thank Dr. Wei Chu from Sichuan University in consideration of Professor Chu Wei’s guidance in the revision of the paper. This work was supported by the Joint Open Fund of Jiangsu Collaborative Innovation Center for Ecological Building Material and Environmental Protection Equipment and Key Laboratory for Advanced Technology in Environmental Protection of Jiangsu Province, under Construction for Volatile Organic Compounds Controlling of Jiangsu Province. This work was also supported by funding for school-level research projects of Yancheng Institute of Technology (154203639).

References

K. Ishaq, B. Mohammed, B. Saleh et al., “Morphology controlled porous poly(lactic acid)/zeolitic imidazolate framework-8 fibrous membranes with superior PM2.5 capture capacity,” Chemical Engineering Journal, vol. 338, pp. 82–91, 2018.
View at: Publisher Site | Google Scholar
G. Xiao, Y. Wang, and T. Kuang, “ZIF-8 based membranes for carbon dioxide capture/separation,” ACS Sustainable Chemistry & Engineering, vol. 5, no. 12, pp. 11204–11214, 2017.
View at: Google Scholar
A. Barjola, J. Escorihuela, A. Andrio, E. Giménez, and V. Compañ, “Enhanced conductivity of composite membranes based on sulfonated poly (ether ether ketone) (SPEEK) with zeolitic imidazolate frameworks (ZIFs),” Nanomaterials, vol. 8, no. 12, pp. 1042–1058, 2018.
View at: Publisher Site | Google Scholar
T. Wu, X. Feng, S. K. Elsaidi, P. K. Thallapally, and M. A. Carreon, “Zeolitic imidazolate framework-8 (ZIF-8) membranes for Kr/Xe separation,” Industrial & Engineering Chemistry Research, vol. 56, no. 6, pp. 1682–1686, 2017.
View at: Publisher Site | Google Scholar
R. Banerjee, A. Phan, B. Wang et al., “High-throughput synthesis of zeolitic imidazolate frameworks and application to CO₂ capture,” Science, vol. 319, no. 5865, pp. 939–943, 2008.
View at: Publisher Site | Google Scholar
Y. Gao, Z. Qiao, S. Zhao, Z. Wang, and J. Wang, “In situsynthesis of polymer grafted ZIFs and application in mixed matrix membrane for CO2separation,” Journal of Materials Chemistry A, vol. 6, no. 7, pp. 3151–3161, 2018.
View at: Publisher Site | Google Scholar
J. An and N. L. Rosi, “Tuning MOF CO₂ adsorption properties via cation exchange,” Journal of the American Chemical Society, vol. 132, no. 16, pp. 5578-5579, 2010.
View at: Publisher Site | Google Scholar
P. Krokidas, M. Castier, and I. G. Economou, “Computational study of ZIF-8 and ZIF-67 performance for separation of gas mixtures,” Journal of Physical Chemistry C, vol. 121, no. 33, pp. 17999–18011, 2017.
View at: Publisher Site | Google Scholar
H. Yang, X. W. He, F. Wang, Y. Kang, and J. Zhang, “Doping copper into ZIF-67 for enhancing gas uptake capacity and visible-light-driven photocatalytic degradation of organic dye,” Journal of Materials Chemistry, vol. 22, no. 41, pp. 21849–21851, 2012.
View at: Publisher Site | Google Scholar
T. T. Isimjan, H. Kazemian, S. Rohani, and A. K. Ray, “Photocatalytic activities of Pt/ZIF-8 loaded highly ordered TiO₂ nanotubes,” Journal of Materials Chemistry, vol. 20, no. 45, pp. 10241–10245, 2010.
View at: Publisher Site | Google Scholar
C. Han, C. Zhang, N. Tymińska, J. R. Schmidt, and D. S. Sholl, “Insights into the stability of zeolitic imidazolate frameworks in humid acidic environments from first-principles calculations,” Journal of Physical Chemistry C, vol. 122, no. 8, pp. 4339–4348, 2018.
View at: Publisher Site | Google Scholar
A. Huang, Q. Liu, N. Wang, and J. Caro, “Organosilica functionalized zeolitic imidazolate framework ZIF-90 membrane for CO₂/CH₄ separation,” Microporous and Mesoporous Materials, vol. 192, no. 3, pp. 18–22, 2014.
View at: Publisher Site | Google Scholar
H. Hayashi, A. P. Côté, H. Furukawa, M. O'Keeffe, and O. M. Yaghi, “Zeolite A imidazolate frameworks,” Nature Materials, vol. 6, no. 7, pp. 501–506, 2007.
View at: Publisher Site | Google Scholar
Z. Wang and S. M. Cohen, “Postsynthetic modification of metal-organic frameworks,” Chemical Society Reviews, vol. 38, no. 5, pp. 1315–1329, 2009.
View at: Publisher Site | Google Scholar
M. J. Ingleson, J. Perez Barrio, J.-B. Guilbaud, Y. Z. Khimyak, and M. J. Rosseinsky, “Framework functionalisation triggers metal complex binding,” Chemical Communications, vol. 23, no. 23, pp. 2680–2682, 2008.
View at: Publisher Site | Google Scholar
R. Kumar, K. Jayaramulu, T. K. Maji, and C. N. Rao, “Hybrid nanocomposites of ZIF-8 with graphene oxide exhibiting tunable morphology, significant CO₂ uptake and other novel properties,” Chemical Communications, vol. 49, no. 43, pp. 4947–4949, 2013.
View at: Publisher Site | Google Scholar
C. Chen, J. Kim, D.-A. Yang, and W.-S. Ahn, “Carbon dioxide adsorption over zeolite-like metal organic frameworks (ZMOFs) having a sod topology: Structure and ion-exchange effect,” Chemical Engineering Journal, vol. 168, no. 3, pp. 1134–1139, 2011.
View at: Publisher Site | Google Scholar
J. Lan, D. Cao, W. Wang, and B. Smit, “Doping of alkali, alkaline-earth, and transition metals in covalent-organic frameworks for enhancing CO₂ capture by first-principles calculations and molecular simulations,” ACS Nano, vol. 4, no. 7, pp. 4225–4237, 2010.
View at: Publisher Site | Google Scholar
H. Fei, J. F. Cahill, K. A. Prather, and S. M. Cohen, “Tandem postsynthetic metal ion and ligand exchange in zeolitic imidazolate frameworks,” Inorganic Chemistry, vol. 52, no. 7, pp. 4011–4016, 2013.
View at: Publisher Site | Google Scholar
F. Nouar, J. Eckert, J. Eubank, P. Forster, and M. Eddaoudi, “Zeolite-like metal-organic frameworks (ZMOFs) as hydrogen storage platform: lithium and magnesium ion-exchange and H(2)-(rho-ZMOF) interaction studies,” Journal of the American Chemical Society, vol. 131, no. 8, pp. 2864–2870, 2009.
View at: Publisher Site | Google Scholar
K. S. Walton, M. B. Abney, and M. Douglas LeVan, “CO₂ adsorption in Y and X zeolites modified by alkali metal cation exchange,” Microporous and Mesoporous Materials, vol. 91, no. 1-3, pp. 78–84, 2006.
View at: Publisher Site | Google Scholar
L. Zhang, J. N. Primera-Pedrozo, and A. J. Hernández-Maldonado, “Thermal detemplation of Na-SAPO-34: effect on Sr²⁺ Ion exchange and CO₂ Adsorption,” Journal of Physical Chemistry C, vol. 114, no. 35, pp. 14755–14762, 2010.
View at: Publisher Site | Google Scholar
R. Chen, J. Yao, Q. Gu et al., “A two-dimensional zeolitic imidazolate framework with a cushion-shaped cavity for CO₂ adsorption,” Chemical Communications, vol. 49, no. 82, pp. 9500–9502, 2013.
View at: Publisher Site | Google Scholar
T. Karanfil and J. E. Kilduff, “Role of granular activated carbon surface chemistry on the adsorption of organic compounds. 1. Priority pollutants,” Environmental Science & Technology, vol. 33, no. 18, pp. 3217–3224, 1999.
View at: Publisher Site | Google Scholar
J. Qian, F. Sun, and L. Qin, “Hydrothermal synthesis of zeolitic imidazolate framework-67 (ZIF-67) nanocrystals,” Materials Letters, vol. 82, pp. 220–223, 2012.
View at: Publisher Site | Google Scholar
A. F. Gross, E. Sherman, and J. J. Vajo, “Aqueous room temperature synthesis of cobalt and zinc sodalite zeolitic imidizolate frameworks,” Dalton Transactions, vol. 41, no. 18, pp. 5458–5460, 2012.
View at: Publisher Site | Google Scholar
N. Maes and E. F. Vansant, “Modification of the porosity of pillared clays by carbon deposition II. Hydrocarbon cracking,” Journal of Porous Materials, vol. 4, no. 1, pp. 5–15, 1997.
View at: Publisher Site | Google Scholar
Y. Yang, W. Z. Li, and H. Y. Xu, “Influence of CeO₂ and Co₃O₄ promoters on carbon deposition and carbon elimination over Ni-based catalysts,” Chinese Journal of Catalysis, vol. 23, no. 6, pp. 517–520, 2002.
View at: Google Scholar
G. Wang, B. Dou, Z. Zhang, J. Wang, H. Liu, and Z. Hao, “Adsorption of benzene, cyclohexane and hexane on ordered mesoporous carbon,” Journal of Environmental Sciences, vol. 30, pp. 65–73, 2015.
View at: Publisher Site | Google Scholar
H. Ma, H. Ren, X. Zou et al., “Novel lithium-loaded porous aromatic framework for efficient CO₂ and H₂ uptake,” Journal of Materials Chemistry A, vol. 1, no. 3, pp. 752–758, 2013.
View at: Publisher Site | Google Scholar
A. J. Hernandez-Maldonado, J. Guerrero-Medina, and V. C. Arce-Gonzalez, “Long range structural and textural changes in [Zn(bdc)(ted) 0.5] upon spontaneous dispersion of LiCl and hysteretic adsorption and desorption of carbon dioxide and hydrogen,” Journal of Materials Chemistry A, vol. 1, no. 6, pp. 2343–2350, 2013.
View at: Publisher Site | Google Scholar
J. Yao, M. He, K. Wang, R. Chen, Z. Zhong, and H. Wang, “High-yield synthesis of zeolitic imidazolate frameworks from stoichiometric metal and ligand precursor aqueous solutions at room temperature,” CrystEngComm, vol. 15, no. 18, pp. 3601–3606, 2013.
View at: Publisher Site | Google Scholar
X. Feng and M. A. Carreon, “Kinetics of transformation on ZIF-67 crystals,” Journal of Crystal Growth, vol. 418, pp. 158–162, 2015.
View at: Publisher Site | Google Scholar
G. Calleja, J. A. Botas, M. Sánchez-Sánchez, and M. G. Orcajo, “Hydrogen adsorption over zeolite-like MOF materials modified by ion exchange,” International Journal of Hydrogen Energy, vol. 35, no. 18, pp. 9916–9923, 2010.
View at: Publisher Site | Google Scholar
M. Kosmulski, “The pH-dependent surface charging and the points of zero charge,” Journal of Colloid and Interface Science, vol. 253, no. 1, pp. 77–87, 2002.
View at: Publisher Site | Google Scholar
H. Zhuo, Q. Li, W. Li, and J. Cheng, “The dual role of pnicogen as Lewis acid and base and the unexpected interplay between the pnicogen bond and coordination interaction in ,” New Journal of Chemistry, vol. 39, no. 3, pp. 2067–2074, 2015.
View at: Publisher Site | Google Scholar
Q. Liu, J. Shi, S. Zheng, M. Tao, Y. He, and Y. Shi, “Kinetics studies of CO₂ Adsorption/Desorption on amine-functionalized multiwalled carbon nanotubes,” Industrial & Engineering Chemistry Research, vol. 53, no. 29, pp. 11677–11683, 2014.
View at: Publisher Site | Google Scholar
X. Wang, L. Chen, and Q. Guo, “Development of hybrid amine-functionalized MCM-41 sorbents for CO₂ capture,” Chemical Engineering Journal, vol. 260, pp. 573–581, 2015.
View at: Publisher Site | Google Scholar
J. Cravillon, S. Münzer, S.-J. Lohmeier, A. Feldhoff, K. Huber, and M. Wiebcke, “Rapid room-temperature synthesis and characterization of nanocrystals of a prototypical zeolitic imidazolate framework,” Chemistry of Materials, vol. 21, no. 8, pp. 1410–1412, 2009.
View at: Publisher Site | Google Scholar
Y. Pan, Y. Liu, G. Zeng, L. Zhao, and Z. Lai, “Rapid synthesis of zeolitic imidazolate framework-8 (ZIF-8) nanocrystals in an aqueous system,” Chemical Communications, vol. 47, no. 7, pp. 2071–2073, 2011.
View at: Publisher Site | Google Scholar
K. K. Gangu, S. Maddila, S. B. Mukkamala, and S. B. Jonnalagadda, “Characteristics of MOF, MWCNT and graphene containing materials for hydrogen storage: a review,” Journal of Energy Chemistry, vol. 30, pp. 132–144, 2019.
View at: Publisher Site | Google Scholar
E. X. Chen, H. Yang, and J. Zhang, “Zeolitic imidazolate framework as formaldehyde gas sensor,” Inorganic Chemistry, vol. 53, no. 11, pp. 5411–5413, 2014.
View at: Publisher Site | Google Scholar

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Copyright © 2020 Fujiao Song et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Journal of Nanomaterials

Ion-Exchanged ZIF-67 Synthesized by One-Step Method for Enhancement of CO2 Adsorption

Abstract

1. Introduction

2. Materials and Methods

2.1. Materials

2.2. Synthesis of the ZIF-67 and Ion-Exchanged ZIF-67

2.3. Characterization and Adsorption Measurements

3. Results and Discussion

3.1. Adsorption Studies

3.2. CO2 Adsorption Mechanism

3.3. CO2 Adsorption-Desorption Isotherms and Cyclic Adsorption-Regeneration Test

3.4. Thermal Stability Characterized by TGA

4. Conclusions

Data Availability

Disclosure

Conflicts of Interest

Authors’ Contributions

Acknowledgments

References

Copyright

Ion-Exchanged ZIF-67 Synthesized by One-Step Method for Enhancement of CO₂ Adsorption

3.2. CO₂ Adsorption Mechanism

3.3. CO₂ Adsorption-Desorption Isotherms and Cyclic Adsorption-Regeneration Test