Next Article in Journal
Virtual Screening of FDA-Approved Drugs against LasR of Pseudomonas aeruginosa for Antibiofilm Potential
Previous Article in Journal
Immunomodulatory Activity and Phytochemical Profile of Infusions from Cleavers Herb
Previous Article in Special Issue
Improved Water-Tree Resistances of SEBS/PP Semi-Crystalline Composites under Crystallization Modifications
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Molecules
Volume 25
Issue 16
10.3390/molecules25163722
molecules-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:
Review

Advances in the Synthesis of Ferrierite Zeolite

by
Hao Xu
1,
Jie Zhu
2,
Longfeng Zhu
2,*,
Enmu Zhou
1 and
Chao Shen
1,*
1
College of Biology and Environmental Engineering, Zhejiang Shuren University, Hangzhou 310015, China
2
College of Biological, Chemical Science and Engineering, Jiaxing University, Jiaxing 314001, China
*
Authors to whom correspondence should be addressed.
Molecules 2020, 25(16), 3722; https://doi.org/10.3390/molecules25163722
Submission received: 20 July 2020 / Revised: 13 August 2020 / Accepted: 13 August 2020 / Published: 14 August 2020
(This article belongs to the Special Issue Molecular Crystals: Structures, Physicalities, and Behaviors (or Dynamics))
Browse Figures
Versions Notes

Abstract

:
As one of the most important porous materials, zeolites with intricate micropores have been widely employed as catalysts for decades due to their large pore volume, high surface area, and good thermal and hydrothermal stabilities. Among them, ferrierite (FER) zeolite with a two-dimensional micropore structure is an excellent heterogeneous catalyst for isomerization, carbonylation, cracking, and so on. In the past years, considering the important industrial application of FER zeolite, great efforts have been made to improve the synthesis of FER zeolite and thus decrease the synthesis cost and enhance catalytic performance. In this review, we briefly summarize the advances in the synthesis of FER zeolite including the development of synthesis routes, the use of organic templates, organotemplate-free synthesis, the strategies of morphology control, and the creation of intra-crystalline mesopores. Furthermore, the synthesis of hetero-atomic FER zeolites such as Fe-FER and Ti-FER has been discussed.

Graphical Abstract

1. Introduction

Zeolites are crystalline microporous materials which have been widely applied on an industrial scale in heterogeneous catalysis, adsorption, separation and ion exchange in the past decades [1,2,3,4,5]. Among them, Ferrierite (FER) zeolite is one of the industrialized types, which has excellent catalytic properties in skeletal isomerization of n-alkene, methanol to olefin, N2O decomposition, CO2 hydrogenation, dehydration of methanol or ethanol, dimethyl ether carbonylation, and so on [6,7,8,9,10,11,12,13,14,15,16].
FER is a medium-pore-size zeolite containing two perpendicular intersecting channels. One is 8-membered ring (MR) channel (3.4 × 5.4 Å) along the [010] direction, and the other one is the 10 MR channel (4.3 × 5.5 Å) along the [001] direction [17,18,19]. Since the first synthetic preparation of FER zeolites in the 1960s, many efforts have been made in the synthesis and modification of FER zeolites in the past decades considering the important industrial application of FER zeolite in skeletal isomerization of n-butene. Therefore, FER zeolites with different elementary composition, morphology, hierarchical structure, acid strength, and catalytic properties have been successfully prepared using different synthesis methods [12,19,20,21,22,23,24,25].
In this review, we briefly summarize the synthesis advances of FER zeolite including the development of synthesis routes, the use of organic templates, organotemplate-free synthesis, the strategies of morphology control, the creation of intra-crystalline mesopores and the isomorphous substitution of skeleton Si and Al atoms with heteroatoms.

2. The Routes for the Synthesis of Aluminosilicate FER Zeolite

Up to now, many routes for synthesizing aluminosilicate FER zeolite (namely ZSM-35) have been developed, including hydrothermal synthesis, solvothermal synthesis, vapor phase transport (VPT) synthesis, transformation synthesis, solid-state synthesis, microwave-assisted synthesis and topotactic condensation of a layered precursor [12,25,26,27,28,29,30,31]. The distinct features of each synthesis routes have been listed in Table 1.
As with many other important zeolites, the earliest and most common synthesis route for aluminosilicate FER zeolites is hydrothermal synthesis, which is performed at very high temperature (above 300 °C) in the presence of Na+-Ca2+, Ca2+-Sr2+-Na+ or Na+-tetramethylammonium (TMA) composite [25,32]. Then, with the employment of new organic templates such as cetyltrimethylammonium, diethanolamine, pyrrolidine (THP) or ethylenediamine (EDA), the synthesis temperature could be reduced to around 150 °C [20,33,34,35]. Obviously, the synthesis process at a relatively low temperature condition effectively reduces the energy consumption and also improves the production safety.
Instead of the conventional water solvent used in the hydrothermal synthesis process, organic solvents could also be employed in the synthesis of zeolites, which is known as solvothermal synthesis. In order to grow large aluminosilicate FER zeolite single crystals, Kuperman et al. replaced the H2O solvent with non-aqueous solvent to control the solubility of the reagent gel particles. This so-called non-aqueous synthesis system included triethylamine (Et3N) as solvent, HF as mineralizer and tetrapropylammonium bromide (TPABr) as an organic template. Giant single crystals of aluminosilicate FER zeolite with the size of around 700 μm were successfully obtained [22]. Moreover, Pang et al. performed the synthesis of aluminosilicate FER zeolites in the alcoholic system in 1995. In ethanol solvent, aluminosilicate FER zeolites could be synthesized using a serious of amine including piperidine (Pi), dibutylamine (DBA), ethylenediamine (EDA) and cinchonine as the organic templates [27].
Later, Matsukata et al. reported a vapor-phase transport (VPT) synthesis route for the preparation of aluminosilicate FER zeolite. In this process, dry aluminosilicate gel was prepared by mixing aging, and drying silica and alumina source. Then, the vapor containing EDA, Et3N and H2O was supplied to the dry-gel at 180 °C for several days (Figure 1). The roles of water and amines in this synthesis system were investigated in detail, giving the result that EDA acted as OSDA while Et3N and H2O promoted crystallization. As a result, the dry-gel could be fully converted into zeolite and thus enhanced both the solid yield and the Si/Al ratio (14.5–15.5) of the product [28]. Long et al. reported a novel VPT synthesis of high-silica FER zeolite (Si/Al = 9.8). In this report, they used the mixture of tetrahydrofuran (THF) and water as a vapor phase for the first time. THF in the vapor phase played the template role, while FER zeolite seeds in the dry-gel and H2O in the vapor phase promoted the crystallization [36].
Transformation synthesis, which is another synthesis route for synthesizing aluminosilicate FER zeolite, was performed in 1998 by Beyer et al. In this work, high-silica FER zeolite (Si/Al = 15–18) could be synthesized by recrystallization of magadiite in the dry state (H2O/SiO2 = 8.7 in the starting mixture) and aqueous suspension (H2O/SiO2 = 40 in the starting mixture) with the piperidine as an organic template. It is worth noting that the crystallization time of aluminosilicate FER zeolite in dry state system was much shorter than that in aqueous suspension. Moreover, the crystal morphology of the two products was different. However, the reasons for the above phenomena were not clarified [29].
From the viewpoint of green chemistry, the use of a solvent in the above synthesis of aluminosilicate FER zeolites would produce a large amount of polluted water, which is not a sustainable manner [42,43,44,45]. Encouragingly, the solvent content in the crystallization of aluminosilicate FER zeolites was significantly reduced using VPT route and transformation synthesis route [28,29,36]. However, in the VPT synthesis route, the preparation of dry-gel still needs a large amount of water as a solvent [28,36]. It is worth noting that the H2O/SiO2 in the above-mentioned dry state transformation synthesis system is still not low enough (8.7) [29]. In 2000, Beyer et al. reported a novel synthesis route for high-silica FER zeolite (Si/Al = 12–35) by solid-state recrystallization of aluminum-containing kanemite varieties using piperidine as an organic template. This work was progressive that water solvent was not necessary in the crystallization of FER zeolite. However, similar to the VPT route, the preparation of kanemite could not avoid the use of a large amount of water solvent [37]. Moreover, Dou et al. reported a solid-transformation synthesis route of aluminosilicate FER zeolite using conventional silica and aluminum source (fumed silica and aluminum sulfate). In this synthesis route, although the H2O/SiO2 ratio was successfully reduced to 2.6, the amount of ethylene diamine (EDA) as an organic template added in the synthesis system was relatively high (EDA/SiO2 = 0.95) [30].
In addition, since the first successful application of microwave-assisted synthesis of ZSM-5 zeolite reported by Mobil researchers in 1988, this synthesis method has attracted a lot of attention because of its unique advantages such as fast crystallization, high efficiency, and simple preparation [46,47,48,49]. Recently, Xu et al. reported a rapid synthesis of aluminosilicate FER zeolites through microwave-assisted route. Comparing to the conventional crystallization time (several days), the crystallization rate was greatly enhanced in this preparation and the aluminosilicate FER zeolite could be obtained within only 2–3 h in the absence of OSDA [31].
Furthermore, considering the bottom-up synthesis concept, FER zeolite could also be obtained by topotactic conversion from its layered precursors. The first layered precursor named as PREFER was synthesized by Marler et al. in fluoride media with the use of a bulky template, 4-amino-2,2,6,6-tetramethylpiperidine. After calcination at around 500 °C, the PREFER layers would link together through condensation reactions and thus transform to 3-dimentional (3D) FER topology [38]. Since then, many other layered precursors of FER zeolite, such as PLS-3 and ICP-2 were gradually obtained by the different synthesis routes [39,40,41].

3. Synthesis of Aluminosilicate FER Zeolite with the Use of the Different Organic Templates

In the zeolite synthesis, the application of organic templates has many advantages such as reducing the crystallization temperature and time, increasing the Si/Al ratio of the products, adjusting the properties of the products and so on. So far, a variety of organic templates, including alkylamines, cyclic amines, and alcohols have been reported to be used in the synthesis of aluminosilicate FER zeolites [6,18,20,26,27,29,32,36,37,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69]. The detailed information of organic templates for synthesizing FER zeolite is shown in Table 2.
Since the 1970s, tetramethylammonium (TMA), ethylenediamine (EDA), and pyrrolidine (THP) were the earliest organic templates used in the synthesis of aluminosilicate FER zeolite [20,32]. For instance, Mobil researchers reported the hydrothermal synthesis of aluminosilicate FER zeolite with the use of EDA or THP [20].
Except for the TMA and EDA as the organic templates for synthesizing FER zeolites, some other alkylamines could also be used as the organic templates in the preparation of aluminosilicate FER zeolites. Examples include the solvothermal synthesis using dibutylamine (DBA) [27], the hydrothermal synthesis with the use of n-butylamine (n-BA) [54], 1,8-diaminooctane (DAO) [55], and isopropylamine (IPA) [56].
Other than the THP as an organic template for synthesizing FER zeolites, some other cyclic molecules, which have the similar molecular structure to THP, such as pyridine (Py) [57,58], piperidine (Pi) [6,29,37], tetrahydrofuran (THF) [26,36,60], N,N-diethyl-cis-2,6-dimethyl piperidinium (DMPi) [18,61] and 1,3-dimethyimidazolium (DMI) [62,63] could also be used as the organic templates in the synthesis of aluminosilicate FER zeolites. For example, in 1989, Smith et al. reported the hydrothermal synthesis of aluminosilicate FER zeolite with the range of Si/Al ratios at 15.1–19.3 using Py as an organic template [57]. Later, in 1999, Martínez et al. successfully synthesized high silica FER zeolite (Si/Al = 59) with the use of Py as an organic template under rotation condition. The obtained high silica FER zeolite exhibited high selectivity as well as high stability during the skeletal isomerization reaction of n-butenes [58]. Moreover, in 1997, a mixture of MOR and FER zeolites were synthesized with the use of Pi as an organic template for the first time [59]. Later, Beyer et al. obtained a pure phase of aluminosilicate FER zeolite by solid-state recrystallization of magadiite or kanemite using Pi as an organic template [29,37]. Recently, a pure phase of aluminosilicate FER zeolite with high crystallinity could be directly synthesized with the use of Pi as an organic template by carefully adjusting the ratio of the starting gel. The obtained product exhibited good catalytic performance in the skeletal isomerization reaction of 1-butene [6]. Meanwhile, Long’s group reported the successful synthesis of FER zeolite with the use of THF as an organic template under the hydrothermal and VPT condition [36]. More recently, we proved that the DMPi molecules could also be used as an organic template for the synthesis of aluminosilicate FER zeolite and thus obtained the nanosheet-like FER zeolite with the thickness at 6–8 nm [61].
Moreover, aluminosilicate FER zeolites could be successfully synthesized using the alcohol molecules as the organic templates as well. For examples, Candamano et al. reported the hydrothermal synthesis of (Fe, Al) FER zeolite with the use of ethylene glycol (EG) [64]. Meng et al. performed the hydrothermal synthesis of aluminosilicate FER zeolite in the presence of a large amount of EG (EG/SiO2 = 7) [65].
In general, it is well-known that the use of different organic templates would affect the properties of the obtained zeolites including Al distribution, acidic strength, morphology and so on, and thus further influence its catalytic performance. In this case, the use of cooperative structure-directing agents (co-SDAs) would attract much attention because the different combinations of the organic templates used in the synthesis could influence the zeolite properties [22,66,70,71,72,73,74]. For example, Perez-Pariente et al. designed a novel synthesis strategy in fluoride medium based on the combination of the small molecules (TMA) with the bulkier molecules (benzylmethylpyrrolidinium, BMP) as the organic templates. Molecular mechanics calculations revealed that TMA molecules sat in the FER cages, while BMP molecules positioned in the 10-MR channels (Figure 2). Following this synthesis strategy, aluminosilicate FER zeolites with the Si/Al ratio in the range of 10–16 were successfully prepared, although the crystallization time was relatively long (at least 10 days) [66]. In 2011, Komarneni et al. prepared the large single crystals of aluminosilicate FER zeolite using the mixed organic molecules (triethylamine (Et3N), TPABr, Py, and propylamine (PA)), while the structure-directing effect of these organic molecules was not mentioned [67]. Meanwhile, Davis et al. reported the synthesis of aluminosilicate FER zeolites using a combination of organic templates including TMA and one of the cyclic amines (THP, hexamethyleneimine (HMI), and 1,4-diazabicyclo [2.2.2] octane (DAB)). In this synthesis process, the structure-function relations between the organic template molecules and aluminum distribution within the FER products were carefully studied, giving a result that the location of acidic sites could be adjusted by the use of different organic templates [68]. Later, Wang et al. also used a combination of TMA and a cyclic amine (Pi) as the cooperative organic templates, resulting in the hierarchical aluminosilicate FER zeolite aggregated by nanosheets morphology [75]. Almeida et al. combined a bulky dicationic ion, 1,6-bis(N-methylpyrrolidinium) hexane (MPH), and a smaller species, TMA as co-SDAs to control the Al distribution in the synthesis of aluminosilicate FER zeolites [69]. Recently, Rima et al. studied the synthesis of FER zeolites through the combined use of TMA and THP as co-SDAs. The result showed that THP plays an important role in the initial nucleation while TMA+ provided both space-filling and basicity capacities in the synthesis of aluminosilicate FER zeolite [71].

4. Organotemplate-Free Synthesis of Aluminosilicate FER Zeolite

Even though the aforementioned works are inspiring, considering the industrial production cost and environmental protection, there is no doubt that the idea of complete avoidance of organic templates in the synthesis is particularly attractive [43,76,77,78,79].
The first example for the organic template-free synthesis of aluminosilicate FER zeolite was achieved by Weitkamp et al. with the addition of FER zeolite seeds. The obtained products possessed good crystallinity, typical blocky morphology and a large number of accessible acid sites. However, the range of Si/Al ratio of the products was narrow (6.6–7.8) [80]. Later, Okubo et al. further optimized the synthesis condition of aluminosilicate FER zeolite without the use of organic template or zeolite seeds. In addition, the cooperative effect of sodium and potassium ions was studied in detail. However, the Si/Al ratio of the obtained products was not mentioned in the article. Considering the Si/Al ratio in the starting gel no more than 10, it is reasonable to assume that the Si/Al ratio of the products would not be higher than 10 [81]. Okubo et al. also mentioned the synthesis of aluminosilicate FER zeolite using itself as seeds without the help of an organic template. In this report, the FER product showed a relatively low Si/Al ratio (7.6) and solid yield (22%) [82].
Despite the great progress for the organic template-free synthesis of aluminosilicate FER zeolite, the obtained product is always Al-rich (Si/Al ratio no more than 10). Normally, high-silica aluminosilicate FER zeolites could be achieved with the assistance of organic templates [83,84,85,86]. In recent years, it was found that aluminosilicate FER zeolites with relatively high Si/Al ratio could be synthesized by adding zeolite seeds with different topologies from FER, which is regarded as a breakthrough for the synthesis of high silica FER zeolite [21,87]. For examples, Xiao et al. reported the first successful synthesis of high-silica aluminosilicate FER zeolite (Si/Al ratio as high as 14.5, designated as ZJM-2) by inducing CDO-structure zeolite building units in the synthesis system in the absence of any organic template. It is well-known that FER and CDO zeolites have the same building units, and UV-Raman spectra demonstrated the possibility that CDO crystals dissolved into smaller building units under hydrothermal treatment. Therefore, by carefully adjusting the chemical composition in the starting gel and crystallization conditions, aluminosilicate FER zeolite with high silica feature was successfully obtained [21]. Later, Liu et al. reported the organotemplate-free and seed-assisted synthesis of high silica aluminosilicate FER (Si/Al = 14.5) with MCM-49 seeds without the common composite building units with FER structure. Furthermore, the solid yield in this synthesis is relatively high (65–85%). The product exhibits good catalytic performance in DME carbonylation to MA reaction. In addition, a possible growth mechanism is proposed based on the hyperpolarized 129Xe Nuclear Magnetic Resonance (NMR) technique (as shown in Figure 3). In this hypothesis, MCM-49 was first dissolved into small fragments in the alkaline gel, then FER framework started to form over MCM-49 through intergrowth connection on the active growth surface (possibly similar 5MR between the two zeolites). This work suggested a new seed-assisted synthesis strategy using the similarity between the seeds and target zeolite [87].

5. Morphology Control Strategies of Aluminosilicate FER Zeolite

As mentioned above, aluminosilicate FER zeolite shows excellent catalytic performances in many reactions because of the abundant acidic sites within its uniform micropores. However, the relatively small (below 1 nm) and sole micropores in aluminosilicate FER zeolite often cause diffusion limitations and thus strongly influence the mass transfer in catalysis. Therefore, the synthesis of aluminosilicate FER zeolite nanocrystals is one of the numerous efforts that have been made to overcome the above drawbacks. The access of smaller crystals not only shortens the diffusion paths for reagent and product molecules, but also enlarges the external surface area and thus provides more accessible acidic sites [73,88,89,90].
The most common strategy for preparing zeolite nanocrystals is introducing organic surfactants [91,92]. In order to synthesize aluminosilicate FER nanocrystals, Corma et al. used Pi and a modified surfactant (cetylmethylpiperidinium bromide) as the organic templates. The long carbon chain in the surfactant limited the crystal growth of FER zeolites along three dimensions, and thus produced the aluminosilicate FER nanocrystals with sizes in the range of 10–20 nm (Figure 4A). Because of the reduction of crystal size along the [001] direction, the access to Brønsted acid sites increased, which enhanced its catalytic activity as well as lifetime in oligomerization of 1-pentene to liquid fuels reaction (Figure 4B) [7]. Very similarly, Xu et al. reported a successful size control strategy of aluminosilicate FER zeolite by adding cetyltrimethyl ammonium bromide (CTAB) into the synthesis system containing Pi as the organic template. In their report, the crystal size could be adjusted from 100 nm to 2 μm [17]. Later, Hensen et al. reported the transformation synthesis of hierarchically porous aluminosilicate FER zeolite consisted of the agglomerated sheets (~9–15 nm thickness) by using the N-methylpyrrolidine and C16H33-[1,2-dimethyl-3-imidazolium] bromide as the organic templates [12]. Moreover, Limtrakul et al. reported the synthesis of hierarchical aluminosilicate FER nanosheet assemblies with a ball-shaped morphology using the THP and 3-(trimethoxysilyl) propyl octadecyl dimethyl ammonium chloride (TPOAC) as the organic templates [93].
Notably, the use of surfactants in the synthesis is costly and would cause inconvenience in the product washing process. Thus, it is highly desirable to design a simple and inexpensive synthesis strategy for the nanosized aluminosilicate FER zeolite using the sole and low-cost small OSDAs. Hong et al. reported a synthesis method for aluminosilicate FER nanoneedles with the use of choline as a sole organic template. However, the morphology control mechanism of this synthesis was not mentioned [94]. Recently, we designed a sole small organic ammonium molecule (N,N-diethyl-cis-2,6-dimethyl piperidinium, DMPi) as both structure-directing agent and crystal growth inhibitor (Figure 5a,b). A theoretical calculation showed that when the concentration of DMPi is relatively high, the DMPi molecules would gather on the {100} surface to reduce the adsorption energy, and thus inhibit the growth of FER framework along the [100] direction. With the employment of DMPi, aluminosilicate FER nanosheets with uniform thickness (6–8 nm) could be successfully synthesized (Figure 5c–h). Furthermore, the thickness of the aluminosilicate FER nanosheets could be easily controlled from 6 to 200 nm by just adjusting the DMP concentration in the starting gel. Very importantly, the above-mentioned aluminosilicate FER nanosheets were proven to have the excellent catalytic performance in skeletal isomerization of n-butene to isobutene, which might be potentially important for industrial application of this ultrathin nanosheet FER zeolite as a catalyst candidate in the near future [18,61].
Another morphology control strategy of aluminosilicate FER zeolite without the help of organic template was presented by Xu et al. using microwave-assisted synthesis process. In this report, the crystal size of aluminosilicate FER zeolites could be controlled in the range of 0.4–3.0 μm by just adjusting the particle size of the seeds (0.1–1.3 μm). At the same time, the morphology of the products was similar to that of the seed zeolites [31]. This synthesis strategy is very efficient and environmentally friendly. However, high pressure would be produced in the closed vessels under hydrothermal and microwave-assisted condition, which should be especially careful.
On the other hand, large crystals of zeolites also attract a lot of interest because of their unique applications in refining structures and elucidating the intrinsic adsorption and diffusion properties. For instance, Weitkamp et al. reported the solvothermal synthesis of large-crystal all-silica, aluminosilicate, and borosilicate FER zeolites (100–600 μm) in fluoride medium using Py as the solvent. The morphology and crystal size of FER zeolites were monitored by the use of the different alkylamines as the organic templates and chemical composition of the starting gels [95]. Komarneni et al. reported the synthesis of aluminosilicate FER large single crystals by hydrothermal method using the mixed organic structure-directing agents (Et3N, THP, PA and TPABr). Notably, the average size of the FER zeolite single crystals would reach to 280 μm, which was very suitable for crystallographic research. However, in this synthesis, ZSM-5 phase could always be found together with FER zeolite, which deserves further investigation [67].

6. Creation of Intracrystalline Mesopores in Aluminosilicate FER Zeolite

Another strategy to overcome the diffusion limitation problem of zeolite catalysts is to create intracrystalline mesopores. The introduction of mesopores (2–50 nm) is beneficial to the mass transfer and thus improves the ability of catalytic conversion of bulky molecules [96,97,98].
Creation of the disordered mesopores in zeolite crystals by post-treatments such as steaming and chemical etching has been reported for a long time [99,100]. As for aluminosilicate FER zeolites, Valtchev et al. mixed aluminosilicate FER crystals with HF-NH4F solutions at the different HF concentration, which led to the formation of mesopores and macropores. After such treatment, the obtained hierarchical aluminosilicate FER zeolite had similar chemical composition and acid properties to its original one [50]. Recently, Catizzone et al. reported the post-synthesis of hierarchical aluminosilicate FER zeolite by sequential treatments with NaAlO2, HCl, and NaOH solutions. The obtained materials exhibit high mesoporous volume, and no significant change on acidity. More importantly, the hierarchical aluminosilicate FER zeolite displayed superiority on methanol conversion in methanol dehydration to dimethyl ether reaction, despite of the formation of by-products at high temperatures [101].
In addition, it is widely accepted that organic surfactants could also be used to create intracrystalline mesopores in zeolites. Typically, Cheng et al. and Khitev et al. both reported the recrystallization of FER zeolite in alkaline solution in the presence of CATB (Figure 6). In these processes, parent aluminosilicate FER was partially dissolved in alkaline medium. Then, the FER fragments reassembled and thus the CTAB molecules insert between the layers. The mesopores could be successfully formed using this method [102,103].
Compared with the above-mentioned recrystallization process, direct synthesis of zeolites with intracrystalline mesopores is more convenient and cost-effective. To date, direct synthesis of mesoporous zeolites with many topologies such as EUO, BEA, AEI, and CHA were successfully achieved [97,104,105,106]. However, despite much progress in the synthesis of hierarchical aluminosilicate FER with intercrystal mesopores formed by crystal aggregation, there is no report for the direct synthesis of aluminosilicate FER zeolite with intracrystalline mesopores, which needs further investigation.

7. Synthesis of Heteroatomic FER Zeolite

In the catalytic application of zeolites, it is desirable to modify the acidity of the zeolite in order to enhance the performance of the zeolite catalysts. Isomorphous substitution of skeleton Si and Al atoms by other elements such as Ge, B, Ga, Fe, Ti and V is one of many good methods to achieve this goal. In that case, heteroatomic FER zeolites with the different elementary composition should be prepared [8,19,107,108,109,110,111,112,113]. The heteroatom contents of heteroatomic FER zeolites are listed in Table 3.
In the late 1980s, an aluminium-free FER zeolite was synthesized hydrothermally in the presence of EDA and boric acid by Gunawardane et al. [19]. The researchers refer to boric acid as a template, and claim the substitution of Si by B in T-positions might occur at that time, which is now widely recognized as a fact. Later, Ga3+ had been successfully incorporated in FER zeolite using the THP as an organic template, resulting in a gallosilicate with FER structure (Si, Ga)-FER [107]. After that, the first synthesis of Fe-FER was also hydrothermally synthesized with the use of THP [108]. Moreover, Kotasthane et al. prepared Fe-FER zeolites with the different Fe/Al ratios and Si/Al ratios. Very interestingly, the Fe-FER samples were found to be active in n-hexane oxidation reactions. Meanwhile, the impacts of synthesis routes and chemical composition of Fe-FER catalysts on the catalytic performance were briefly investigated [109]. Recently, because of the severe NOx pollution, Fe-substituted zeolites were employed as the efficient catalysts in the direct N2O decomposition reaction. Among all the Fe-substituted zeolites, Fe-FER was referred to as the best direct N2O decomposition catalyst [8]. Furthermore, Stockenhuber et al. compared the activity and selectivity for partial oxidation of methane using N2O as oxidant over Fe-ZSM-5, Fe-Beta, and Fe-FER catalysts with similar iron concentrations. The catalytic activity studies showed that Fe-FER was the most active catalyst based on methane and N2O conversion (Figure 7) [110]. However, the concentration of framework Al atoms in the zeolite catalysts was different, which led to the different concentration of acid sites in the catalysts and thus influence the catalytic results.
In 1998, Kotasthane et al. prepared a new family of titanium silicate FER (Ti-FER) zeolite using solvothermal synthesis method in the presence of silica-FER seeds [111]. Very similarly, the first successful synthesis of vanadium silicates with FER structure (V-FER) was obtained using a similar solvothermal synthesis route. Electron Paramagnetic Resonance (EPR) spectroscopy confirmed that some of the V4+ was in distorted octahedral positions, while Ultraviolet and visible spectrophotometry (UV-vis) and NMR spectroscopy confirmed the presence of tetrahedral V5+ species in the frameworks. Moreover, the V-FER exhibited good catalytic properties in toluene oxidation reaction [112].
In addition, another novel synthesis of Ti-FER zeolite was performed by Corma et al. In this report, the titanium-containing laminar analogue TiPREFER was directly synthesized with the use of 4-amino-2,2,6,6-tetramethylpiperidine and HF. After calcination of TiPREFER, the Ti-FER was successfully obtained [113]. However, the obtained Ti-FER presented the low catalytic activity and epoxide selectivity in hex-1-ene epoxidation, which should be further investigated.

8. Summary and Future Prospects

In this review, the synthesis of FER zeolite with different methods is discussed in detail. The synthesis routes such as hydrothermal synthesis, solvothermal synthesis, vapor-phase transport, transformation synthesis, solid-transformation synthesis, microwave-assisted synthesis and topotactic conversion are summarized. In addition, the use of different organic templates including alkylamines, cyclic amines, alcohol molecules, and cooperative structure-directing agents are listed separately. Moreover, the development of environmentally friendly organotemplate-free synthesis routes is discussed. Furthermore, the comparisons of different morphology control strategies such as introducing organic surfactants, designing organic template molecules and adjusting the particle size of the zeolite seeds are made. The creation of intracrystalline mesopores through post-treatment or recrystallization with organic surfactant is introduced. Finally, the isomorphous substitution of skeleton atoms of FER zeolite with B, Ga, Fe, Ti, or V atoms is presented.
Despite that, much progress has been made in the synthesis and application of FER zeolites these years, more sustainable synthesis routes, such as the combined strategy of both organotemplate-free and solvent-free routes, and the combined strategy of microwave-assisted synthesis with solvent-free synthesis could be considered. Moreover, the sustainable and effective morphology control strategy and mesopore introduction strategy should be developed. More efforts for preparation of FER zeolite in both fundamental research and industrial production should be made in the future.

Author Contributions

Conceptualization, H.X. and L.Z.; investigation, J.Z. and E.Z.; writing—original draft preparation, H.X.; writing—review and editing, L.Z. and C.S. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by Zhejiang Shuren University Basic Scientific Research Special Funds (2020XZ011), National Natural Science Foundation of China (21802053 and 21773094), and Talent Introduction Project of Zhejiang Shuren University (2019R022).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Davis, M.E. Ordered Porous Materials for Emerging Applications. Nature 2002, 417, 813–821. [Google Scholar] [CrossRef] [PubMed]
  2. Shi, J.; Wang, Y.; Yang, W.; Tang, Y.; Xie, Z. Recent Advances of Pore System Construction in Zeolite-Catalyzed Chemical Industry Processes. Chem. Soc. Rev. 2015, 44, 8877–8903. [Google Scholar] [CrossRef] [PubMed]
  3. Moliner, M.; Martínez, C.; Corma, A. Synthesis Strategies for Preparing Useful Small Pore Zeolites and Zeotypes for Gas Separations and Catalysis. Chem. Mater. 2014, 26, 246–258. [Google Scholar] [CrossRef]
  4. Xiao, F.-S.; Meng, X. (Eds.) Green chemistry and sustainable technology. In Zeolites in Sustainable Chemistry: Synthesis, Characterization and Catalytic Applications; Springer: Berlin/Heidelberg, Germany, 2016. [Google Scholar]
  5. Davis, M.E.; Lobo, R.F. Zeolite and Molecular Sieve Synthesis. Chem. Mater. 1992, 4, 756–768. [Google Scholar] [CrossRef]
  6. Chu, W.; Chen, F.; Guo, C.; Li, X.; Zhu, X.; Gao, Y.; Xie, S.; Liu, S.; Jiang, N.; Xu, L. Synthesis of FER Zeolite with Piperidine as Structure-Directing Agent and Its Catalytic Application. Chin. J. Catal. 2017, 38, 1880–1887. [Google Scholar] [CrossRef]
  7. Margarit, V.J.; Díaz-Rey, M.R.; Navarro, M.T.; Martínez, C.; Corma, A. Direct Synthesis of Nano-Ferrierite along the 10-Ring-Channel Direction Boosts Their Catalytic Behavior. Angew. Chem. 2018, 130, 3517–3521. [Google Scholar] [CrossRef]
  8. Lim, J.B.; Cha, S.H.; Hong, S.B. Direct N2O Decomposition over Iron-Substituted Small-Pore Zeolites with Different Pore Topologies. Appl. Catal. B Environ. 2019, 243, 750–759. [Google Scholar] [CrossRef]
  9. Roth, W.J.; Nachtigall, P.; Morris, R.E.; Čejka, J. Two-Dimensional Zeolites: Current Status and Perspectives. Chem. Rev. 2014, 114, 4807–4837. [Google Scholar] [CrossRef]
  10. Sulikowski, B.; Janas, J.; Haber, J.; Kubacka, A.; Wloch, E.; Olejniczak, Z. The Synergetic Effect of Cobalt and Indium in Ferrierite Catalysts for Selective Catalytic Reduction of Nitric Oxide with Methane. Chem. Commun. 1998, 2755–2756. [Google Scholar] [CrossRef]
  11. Park, S.Y.; Shin, C.-H.; Bae, J.W. Selective Carbonylation of Dimethyl Ether to Methyl Acetate on Ferrierite. Catal. Commun. 2016, 75, 28–31. [Google Scholar] [CrossRef]
  12. Bolshakov, A.; van de Poll, R.; van Bergen-Brenkman, T.; Wiedemann, S.C.C.; Kosinov, N.; Hensen, E.J.M. Hierarchically Porous FER Zeolite Obtained via FAU Transformation for Fatty Acid Isomerization. Appl. Catal. B Environ. 2020, 263, 118356. [Google Scholar] [CrossRef]
  13. Park, S.J.; Jang, H.-G.; Lee, K.-Y.; Cho, S.J. Improved Methanol-to-Olefin Reaction Selectivity and Catalyst Life by CeO2 Coating of Ferrierite Zeolite. Microporous Mesoporous. Mater. 2018, 256, 155–164. [Google Scholar] [CrossRef]
  14. Arora, S.S.; Shi, Z.; Bhan, A. Mechanistic Basis for Effects of High-Pressure H2 Cofeeds on Methanol-to-Hydrocarbons Catalysis over Zeolites. ACS Catal. 2019, 9, 6407–6414. [Google Scholar] [CrossRef]
  15. Frusteri, F.; Migliori, M.; Cannilla, C.; Frusteri, L.; Catizzone, E.; Aloise, A.; Giordano, G.; Bonura, G. Direct CO2-to-DME Hydrogenation Reaction: New Evidences of a Superior Behaviour of FER-Based Hybrid Systems to Obtain High DME Yield. J. CO2 Util. 2017, 18, 353–361. [Google Scholar] [CrossRef]
  16. Catizzone, E.; Daele, S.V.; Bianco, M.; Di Michele, A.; Aloise, A.; Migliori, M.; Valtchev, V.; Giordano, G. Catalytic Application of Ferrierite Nanocrystals in Vapour-Phase Dehydration of Methanol to Dimethyl Ether. Appl. Catal. B Environ. 2019, 243, 273–282. [Google Scholar] [CrossRef]
  17. Wang, Y.; Gao, Y.; Chu, W.; Zhao, D.; Chen, F.; Zhu, X.; Li, X.; Liu, S.; Xie, S.; Xu, L. Synthesis and Catalytic Application of FER Zeolites with Controllable Size. J. Mater. Chem. A 2019, 7, 7573–7580. [Google Scholar] [CrossRef]
  18. Xu, H.; Yu, Y.; Zhu, L.; Bian, C.; Zhai, H.; Tong, J.; Wu, H.; Shen, C. Preparation of Aluminosilicate Ferrierite Zeolite Nanosheets with Controllable Thickness in the Presence of a Sole Organic Structure Directing Agent. Molecules 2020, 25, 771. [Google Scholar] [CrossRef] [Green Version]
  19. Gies, H.; Gunawardane, R.P. One-Step Synthesis, Properties and Crystal Structure of Aluminium-Free Ferrierite. Zeolites 1987, 7, 442–445. [Google Scholar] [CrossRef]
  20. Plank, C.J.; Rosinski, E.J. Crystalline Zeolite and Method of Preparing Same. U.S. Patent 4016245, 5 April 1977. [Google Scholar]
  21. Zhang, H.; Guo, Q.; Ren, L.; Yang, C.; Zhu, L.; Meng, X.; Li, C.; Xiao, F.-S. Organotemplate-Free Synthesis of High-Silica Ferrierite Zeolite Induced by CDO-Structure Zeolite Building Units. J. Mater. Chem. 2011, 21, 9494. [Google Scholar] [CrossRef]
  22. Kuperman, A. Non-Aqueous Synthesis of Giant Crystals of Zeolites and Molecular Sieves. Nature 1993, 365, 239–242. [Google Scholar] [CrossRef]
  23. He, M.; Zhang, J.; Liu, R.; Sun, X.; Chen, B. The Distribution and Strength of Brönsted Acid Sites on the Multi-Aluminum Model of FER Zeolite: A Theoretical Study. Catalysts 2017, 7, 11. [Google Scholar] [CrossRef]
  24. Liu, B.; García-Pérez, E.; Dubbeldam, D.; Smit, B.; Calero, S. Understanding Aluminum Location and Non-Framework Ions Effects on Alkane Adsorption in Aluminosilicates: A Molecular Simulation Study. J. Phys. Chem. C 2007, 111, 10419–10426. [Google Scholar] [CrossRef]
  25. Hawkins, D.B. Zeolite Studies, I. Synthesis of Some Alkaline Earth Zeolites. Mater. Res. Bull. 1967, 2, 951–958. [Google Scholar] [CrossRef]
  26. Guo, G.; Long, Y.; Sun, Y. Synthesis of FER Type Zeolite with Tetrahydrofuran as the Template. Chem. Commun. 2000, 1893–1894. [Google Scholar] [CrossRef]
  27. Du, H.; Qiu, S.; Pang, W. Syntheses of Ferrierite and Mordenite Zeolites from Dried Gel in Alcoholic System. Chem. Res. Chin. Univ. 1995, 11, 364–366. [Google Scholar]
  28. Matsukata, M.; Nishiyama, N.; Ueyama, K. Crystallization of FER and MFI Zeolites by a Vapor-Phase Transport Method. Microporous Mater. 1996, 7, 109–117. [Google Scholar] [CrossRef]
  29. Pál-Borbély, G.; Beyer, H.K.; Kiyozumi, Y.; Mizukami, F. Synthesis and Characterization of a Ferrierite Made by Recrystallization of an Aluminium-Containing Hydrated Magadiite. Microporous Mesoporous Mater. 1998, 22, 57–68. [Google Scholar] [CrossRef]
  30. Pan, R.; Jia, M.; Li, Y.; Li, X.; Dou, T. In Situ Delamination of Ferrierite Zeolite and Its Performance in the Catalytic Cracking of C4 Hydrocarbons. Chin. J. Chem. Eng. 2014, 22, 1237–1242. [Google Scholar] [CrossRef]
  31. Wei, P.; Zhu, X.; Wang, Y.; Chu, W.; Xie, S.; Yang, Z.; Liu, X.; Li, X.; Xu, L. Rapid Synthesis of Ferrierite Zeolite through Microwave Assisted Organic Template Free Route. Microporous Mesoporous Mater. 2019, 279, 220–227. [Google Scholar] [CrossRef]
  32. Kibby, C. Composition and Catalytic Properties of Synthetic Ferrierite. J. Catal. 1974, 35, 256–272. [Google Scholar] [CrossRef]
  33. Borade, R.B.; Clearfield, A. Synthesis of ZSM-35 Using Trimethylcetylammonium Hydroxide as a Template. Zeolites 1994, 14, 458–461. [Google Scholar] [CrossRef]
  34. Forbes, N.R.; Rees, L.V.C. The Synthesis of Ferrierite, ZSM-5, and Theta-1 in the Presence of Diethanolamine: Experimental. Zeolites 1995, 15, 444–451. [Google Scholar] [CrossRef]
  35. Xu, W.-Q.; Yin, Y.-G.; Suib, S.L.; Edwards, J.C.; OYoung, C.-L. n-Butene Skeletal Isomerization to Isobutylene on Shape Selective Catalysts: Ferrierite/ZSM-35. J. Phys. Chem. 1995, 99, 9443–9451. [Google Scholar] [CrossRef]
  36. Cheng, X.; Wang, J.; Guo, J.; Sun, J.; Long, Y. High-Silica Ferrierite Zeolite Self-Transformed from Aluminosilicate Gel. ChemPhysChem 2006, 7, 1198–1202. [Google Scholar] [CrossRef] [PubMed]
  37. Pál-Borbély, G.; Szegedi, Á.; Beyer, H.K. Solid-State Recrystallization of Aluminum-Containing Kanemite Varieties to Ferrierite. Microporous Mesoporous Mater. 2000, 35–36, 573–584. [Google Scholar] [CrossRef]
  38. Schreyeck, L.; Caullet, P.; Mougenel, J.C.; Guth, J.L.; Marler, B. PREFER: A New Layered (Alumino) Silicate Precursor of FER-Type Zeolite. Microporous Mater. 1996, 6, 259–271. [Google Scholar] [CrossRef]
  39. Yang, B.; Jiang, J.; Xu, H.; Liu, Y.; Peng, H.; Wu, P. Selective Skeletal Isomerization of 1-Butene over FER-Type Zeolites Derived from PLS-3 Lamellar Precursors. Appl. Catal. A Gen. 2013, 455, 107–113. [Google Scholar] [CrossRef]
  40. Gálvez, P.; Bernardo-Maestro, B.; Vos, E.; Díaz, I.; López-Arbeloa, F.; Pérez-Pariente, J.; Gómez-Hortigüela, L. ICP-2: A New Hybrid Organo-Inorganic Ferrierite Precursor with Expanded Layers Stabilized by π–π Stacking Interactions. J. Phys. Chem. C 2017, 121, 24114–24127. [Google Scholar] [CrossRef] [Green Version]
  41. Roth, W.J.; Gil, B.; Makowski, W.; Sławek, A.; Grzybek, J.; Kubu, M.; Čejka, J. Interconversion of the CDO Layered Precursor ZSM-55 between FER and CDO Frameworks by Controlled Deswelling and Reassembly. Chem. Mater. 2016, 28, 3616–3619. [Google Scholar] [CrossRef]
  42. Meng, X.; Xiao, F.-S. Green Routes for Synthesis of Zeolites. Chem. Rev. 2014, 114, 1521–1543. [Google Scholar] [CrossRef]
  43. Wu, Q.; Wang, X.; Qi, G.; Guo, Q.; Pan, S.; Meng, X.; Xu, J.; Deng, F.; Fan, F.; Feng, Z.; et al. Sustainable Synthesis of Zeolites without Addition of Both Organotemplates and Solvents. J. Am. Chem. Soc. 2014, 136, 4019–4025. [Google Scholar] [CrossRef] [PubMed]
  44. Meng, X.; Wu, Q.; Chen, F.; Xiao, F.-S. Solvent-Free Synthesis of Zeolite Catalysts. Sci. China Chem. 2015, 58, 6–13. [Google Scholar] [CrossRef]
  45. Wu, Q.; Ma, Y.; Wang, S.; Meng, X.; Xiao, F.-S. 110th Anniversary: Sustainable Synthesis of Zeolites: From Fundamental Research to Industrial Production. Ind. Eng. Chem. Res. 2019, 58, 11653–11658. [Google Scholar] [CrossRef]
  46. Chu, P.; Dwyer, F.G.; Vartuli, J.C. Crystallization Method Employing Microwave Radiation. U.S. Patent 4778666, 18 October 1988. [Google Scholar]
  47. Nasser, G.A.; Muraza, O.; Nishitoba, T.; Malaibari, Z.; Yamani, Z.H.; Al-Shammari, T.K.; Yokoi, T. Microwave-Assisted Hydrothermal Synthesis of CHA Zeolite for Methanol-to-Olefins Reaction. Ind. Eng. Chem. Res. 2019, 58, 60–68. [Google Scholar] [CrossRef]
  48. Shalmani, F.M.; Askari, S.; Halladj, R. Microwave Synthesis of SAPO Molecular Sieves. Rev. Chem. Eng. 2013, 29. [Google Scholar] [CrossRef]
  49. Rao, K.J.; Vaidhyanathan, B.; Ganguli, M.; Ramakrishnan, P.A. Synthesis of Inorganic Solids Using Microwaves. Chem. Mater. 1999, 11, 882–895. [Google Scholar] [CrossRef]
  50. Chen, X.; Todorova, T.; Vimont, A.; Ruaux, V.; Qin, Z.; Gilson, J.-P.; Valtchev, V. In Situ and Post-Synthesis Control of Physicochemical Properties of FER-Type Crystals. Microporous Mesoporous Mater. 2014, 200, 334–342. [Google Scholar] [CrossRef]
  51. Ahedi, R.K.; Kotasthane, A.N. Studies in the Crystallization of Ferrierite (FER) Type Zeolites in Presence of Promoting Medium. J. Porous Mater. 1997, 9. [Google Scholar] [CrossRef]
  52. Ahedi, R.K.; Kotasthane, A.N.; Rao, B.S.; Manna, A.; Kulkarni, B.D. Synthesis of Ferrierite-Type Zeolite in the Presence of a Catalytic Amount of Pyrrolidine and Sodium Bis(2-Ethyhlhexyl) Sulfosuccinate. J. Colloid Interface Sci. 2001, 236, 47–51. [Google Scholar] [CrossRef]
  53. Khomane, R.B.; Kulkarni, B.D.; Ahedi, R.K. Synthesis and Characterization of Ferrierite-Type Zeolite in the Presence of Nonionic Surfactants. J. Colloid Interface Sci. 2001, 236, 208–213. [Google Scholar] [CrossRef]
  54. Zhang, S.; Liu, X.; Zhang, Y.; Lv, T.; Zheng, J.; Gao, W.; Liu, X.; Cui, M.; Meng, C. Study on the Synthesis of MFI and FER in the Presence of N-Butylamine and the Property of n-Butylamine in a Confined Region of Zeolites. RSC Adv. 2016, 6, 114808–114817. [Google Scholar] [CrossRef]
  55. Catizzone, E.; Migliori, M.; Mineva, T.; van Daele, S.; Valtchev, V.; Giordano, G. New Synthesis Routes and Catalytic Applications of Ferrierite Crystals. Part 1: 1,8-Diaminooctane as a New OSDA. Microporous Mesoporous Mater. 2020, 296, 109987. [Google Scholar] [CrossRef]
  56. Shen, K.; Huang, X.; Wang, J.; Chen, Z.; Yu, Y.; Tang, Z.; Liu, Y. Synthesis of FER/MFI Composite Zeolite Using Isopropylamine as a Structure-Directing Agent. Microporous Mesoporous Mater. 2020, 297, 110027. [Google Scholar] [CrossRef]
  57. Smith, W.J.; Dewing, J.; Dwyer, J. Zeolite Synthesis in the SiO2-Al2O3-Na2O-Pyridine-H2O System. J. Chem. Soc. Faraday Trans. 1989, 85, 3623–3628. [Google Scholar] [CrossRef]
  58. Asensi, M.A.; Martínez, A. Selective Isomerization of n-Butenes to Isobutene on High Si/Al Ratio Ferrierite in the Absence of Coke Deposits: Implications on the Reaction Mechanism. Appl. Catal. A Gen. 1999, 183, 155–165. [Google Scholar] [CrossRef]
  59. Jongkind, H.; Datema, K.P.; Nabuurs, S.; Seive, A.; Stork, W.H.J. Synthesis and Characterisation of Zeolites Using Saturated Cyclic Amines as Structure-Directing Agents. Microporous Mater. 1997, 10, 149–161. [Google Scholar] [CrossRef]
  60. Qian, B.; Guo, G.; Wang, X.; Zeng, Y.; Sun, Y.; Long, Y. Templating of High-Silica Zeolites by Tetrahydrofuran in the Na2O–SiO2–Al2O3–H2O System. Phys. Chem. Chem. Phys. 2001, 3, 4164–4169. [Google Scholar] [CrossRef]
  61. Xu, H.; Chen, W.; Zhang, G.; Wei, P.; Wu, Q.; Zhu, L.; Meng, X.; Li, X.; Fei, J.; Han, S.; et al. Ultrathin Nanosheets of Aluminosilicate FER Zeolites Synthesized in the Presence of a Sole Small Organic Ammonium. J. Mater. Chem. A 2019, 7, 16671–16676. [Google Scholar] [CrossRef]
  62. Vinaches, P.; Bernardo-Gusmão, K.; Pergher, S. An Introduction to Zeolite Synthesis Using Imidazolium-Based Cations as Organic Structure-Directing Agents. Molecules 2017, 22, 1307. [Google Scholar] [CrossRef]
  63. Schmidt, J.E.; Deimund, M.A.; Xie, D.; Davis, M.E. Synthesis of RTH-Type Zeolites Using a Diverse Library of Imidazolium Cations. Chem. Mater. 2015, 27, 3756–3762. [Google Scholar] [CrossRef]
  64. Candamano, S.; Frontera, P.; Kora´nyi, T.I.; Macario, A.; Crea, F.; Nagy, J.B. Characterization of (Fe, Al) FER Synthesized in Presence of Ethylene Glycol and Ethylene Diamine. Microporous Mesoporous Mater. 2010, 127, 9–16. [Google Scholar] [CrossRef]
  65. Zhang, S.; Cui, M.; Zhang, Y.; Zheng, J.; Lv, T.; Gao, W.; Liu, X.; Meng, C. Study on the Synthesis of FER and SOD in the Presence of Ethylene Glycol and the Oxidation Transformation of Ethylene Glycol in a Confined Region of Zeolites. J. Alloys Compd. 2017, 696, 788–794. [Google Scholar] [CrossRef]
  66. Pinar, A.B.; Gomez-Hortiguela, L.; Perez-Pariente, J. Cooperative Structure Directing Role of the Cage-Forming Tetramethylammonium Cation and the Bulkier Benzylmethylpyrrolidinium in the Synthesis of Zeolite Ferrierite. Chem. Mater. 2007, 19, 5617–5626. [Google Scholar] [CrossRef]
  67. Kim, S.H.; Komarneni, S.; Heo, N.H. ZSM-5 and Ferrierite Single Crystals with Lower Si/Al Ratios: Synthesis and Single-Crystal Synchrotron X-ray Diffraction Studies. Microporous Mesoporous Mater. 2011, 143, 243–248. [Google Scholar] [CrossRef]
  68. Román-Leshkov, Y.; Moliner, M.; Davis, M.E. Impact of Controlling the Site Distribution of Al Atoms on Catalytic Properties in Ferrierite-Type Zeolites. J. Phys. Chem. C 2011, 115, 1096–1102. [Google Scholar] [CrossRef]
  69. Almeida, R.K.S.; Gómez-Hortigüela, L.; Pinar, A.B.; Peréz-Pariente, J. Synthesis of Ferrierite by a New Combination of Co-Structure-Directing Agents: 1,6-Bis(n-methylpyrrolidinium)hexane and Tetramethylammonium. Microporous Mesoporous Mater. 2016, 232, 218–226. [Google Scholar] [CrossRef]
  70. Martínez-Franco, R.; Moliner, M.; Thogersen, J.R.; Corma, A. Efficient One-Pot Preparation of Cu-SSZ-13 Materials Using Cooperative OSDAs for Their Catalytic Application in the SCR of NOx. ChemCatChem 2013, 5, 3316–3323. [Google Scholar] [CrossRef]
  71. Rima, D.; Djamal, D.; Fatiha, D. Synthesis of High Silica Zeolites Using a Combination of Pyrrolidine and Tetramethylammonium as Template. Mater. Res. Express 2018, 6, 035017. [Google Scholar] [CrossRef]
  72. Jiang, J.; Jorda, J.L.; Yu, J.; Baumes, L.A.; Mugnaioli, E.; Diaz-Cabanas, M.J.; Kolb, U.; Corma, A. Synthesis and Structure Determination of the Hierarchical Meso-Microporous Zeolite ITQ-43. Science 2011, 333, 1131–1134. [Google Scholar] [CrossRef]
  73. Choi, M.; Na, K.; Kim, J.; Sakamoto, Y.; Terasaki, O.; Ryoo, R. Stable Single-Unit-Cell Nanosheets of Zeolite MFI as Active and Long-Lived Catalysts. Nature 2009, 461, 246–249. [Google Scholar] [CrossRef]
  74. Zhu, X.; Hofmann, J.P.; Mezari, B.; Kosinov, N.; Wu, L.; Qian, Q.; Weckhuysen, B.M.; Asahina, S.; Ruiz-Martínez, J.; Hensen, E.J.M. Trimodal Porous Hierarchical SSZ-13 Zeolite with Improved Catalytic Performance in the Methanol-to-Olefins Reaction. ACS Catal. 2016, 6, 2163–2177. [Google Scholar] [CrossRef]
  75. Xue, T.; Liu, H.; Wang, Y.M. Synthesis of Hierarchical Ferrierite Using Piperidine and Tetramethylammonium Hydroxide as Cooperative Structure-Directing Agents. RSC Adv. 2015, 5, 12131–12138. [Google Scholar] [CrossRef]
  76. Ng, E.-P.; Chateigner, D.; Bein, T.; Valtchev, V.; Mintova, S. Capturing Ultrasmall EMT Zeolite from Template-Free Systems. Science 2012, 335, 70–73. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  77. Goel, S.; Zones, S.I.; Iglesia, E. Synthesis of Zeolites via Interzeolite Transformations without Organic Structure-Directing Agents. Chem. Mater. 2015, 27, 2056–2066. [Google Scholar] [CrossRef]
  78. Awala, H.; Gilson, J.-P.; Retoux, R.; Boullay, P.; Goupil, J.-M.; Valtchev, V.; Mintova, S. Template-Free Nanosized Faujasite-Type Zeolites. Nat. Mater. 2015, 14, 447–451. [Google Scholar] [CrossRef] [PubMed]
  79. Xie, B.; Song, J.; Ren, L.; Ji, Y.; Li, J.; Xiao, F.-S. Organotemplate-Free and Fast Route for Synthesizing Beta Zeolite. Chem. Mater. 2008, 20, 4533–4535. [Google Scholar] [CrossRef]
  80. Rakoczy, R.A.; Breuninger, M.; Hunger, M.; Traa, Y.; Weitkamp, J. Template-Free Synthesis of Zeolite Ferrierite and Characterization of Its Acid Sites. Chem. Eng. Technol. 2002, 25, 273–275. [Google Scholar] [CrossRef]
  81. Suzuki, Y.; Wakihara, T.; Itabashi, K.; Ogura, M.; Okubo, T. Cooperative Effect of Sodium and Potassium Cations on Synthesis of Ferrierite. Top. Catal. 2009, 52, 67–74. [Google Scholar] [CrossRef]
  82. Itabashi, K.; Kamimura, Y.; Iyoki, K.; Shimojima, A.; Okubo, T. A Working Hypothesis for Broadening Framework Types of Zeolites in Seed-Assisted Synthesis without Organic Structure-Directing Agent. J. Am. Chem. Soc. 2012, 134, 11542–11549. [Google Scholar] [CrossRef]
  83. Jo, D.; Ryu, T.; Park, G.T.; Kim, P.S.; Kim, C.H.; Nam, I.-S.; Hong, S.B. Synthesis of High-Silica LTA and UFI Zeolites and NH3–SCR Performance of Their Copper-Exchanged Form. ACS Catal. 2016, 6, 2443–2447. [Google Scholar] [CrossRef]
  84. Boal, B.W.; Schmidt, J.E.; Deimund, M.A.; Deem, M.W.; Henling, L.M.; Brand, S.K.; Zones, S.I.; Davis, M.E. Facile Synthesis and Catalysis of Pure-Silica and Heteroatom LTA. Chem. Mater. 2015, 27, 7774–7779. [Google Scholar] [CrossRef] [Green Version]
  85. Sasaki, H.; Oumi, Y.; Itabashi, K.; Lu, B.; Teranishi, T.; Sano, T. Direct Hydrothermal Synthesis and Stabilization of High-Silica Mordenite (Si:Al = 25) Using Tetraethylammonium and Fluoride Ions. J. Mater. Chem. 2003, 13, 1173–1179. [Google Scholar] [CrossRef]
  86. Sonoda, T.; Maruo, T.; Yamasaki, Y.; Tsunoji, N.; Takamitsu, Y.; Sadakane, M.; Sano, T. Synthesis of High-Silica AEI Zeolites with Enhanced Thermal Stability by Hydrothermal Conversion of FAU Zeolites, and Their Activity in the Selective Catalytic Reduction of NOx with NH3. J. Mater. Chem. A 2015, 3, 857–865. [Google Scholar] [CrossRef]
  87. Wang, L.; Tian, P.; Yuan, Y.; Yang, M.; Fan, D.; Zhou, H.; Zhu, W.; Xu, S.; Liu, Z. Seed-Assisted Synthesis of High Silica ZSM-35 through Interface-Induced Growth over MCM-49 Seeds. Microporous Mesoporous Mater. 2014, 196, 89–96. [Google Scholar] [CrossRef]
  88. Na, K.; Choi, M.; Park, W.; Sakamoto, Y.; Terasaki, O.; Ryoo, R. Pillared MFI Zeolite Nanosheets of a Single-Unit-Cell Thickness. J. Am. Chem. Soc. 2010, 132, 4169–4177. [Google Scholar] [CrossRef]
  89. Li, R.; Linares, N.; Sutjianto, J.G.; Chawla, A.; Garcia-Martinez, J.; Rimer, J.D. Ultrasmall Zeolite L Crystals Prepared from Highly Interdispersed Alkali-Silicate Precursors. Angew. Chem. Int. Ed. 2018, 57, 11283–11288. [Google Scholar] [CrossRef] [Green Version]
  90. Valtchev, V.; Tosheva, L. Porous Nanosized Particles: Preparation, Properties, and Applications. Chem. Rev. 2013, 113, 6734–6760. [Google Scholar] [CrossRef]
  91. Park, W.; Yu, D.; Na, K.; Jelfs, K.E.; Slater, B.; Sakamoto, Y.; Ryoo, R. Hierarchically Structure-Directing Effect of Multi-Ammonium Surfactants for the Generation of MFI Zeolite Nanosheets. Chem. Mater. 2011, 23, 5131–5137. [Google Scholar] [CrossRef]
  92. Emdadi, L.; Wu, Y.; Zhu, G.; Chang, C.-C.; Fan, W.; Pham, T.; Lobo, R.F.; Liu, D. Dual Template Synthesis of Meso- and Microporous MFI Zeolite Nanosheet Assemblies with Tailored Activity in Catalytic Reactions. Chem. Mater. 2014, 26, 1345–1355. [Google Scholar] [CrossRef]
  93. Wuamprakhon, P.; Wattanakit, C.; Warakulwit, C.; Yutthalekha, T.; Wannapakdee, W.; Ittisanronnachai, S.; Limtrakul, J. Direct Synthesis of Hierarchical Ferrierite Nanosheet Assemblies via an Organosilane Template Approach and Determination of Their Catalytic Activity. Microporous Mesoporous Mater. 2016, 219, 1–9. [Google Scholar] [CrossRef]
  94. Lee, Y.; Park, M.B.; Kim, P.S.; Vicente, A.; Fernandez, C.; Nam, I.-S.; Hong, S.B. Synthesis and Catalytic Behavior of Ferrierite Zeolite Nanoneedles. ACS Catal. 2013, 3, 617–621. [Google Scholar] [CrossRef]
  95. Marthala, V.R.R.; Hunger, M.; Kettner, F.; Krautscheid, H.; Chmelik, C.; Kärger, J.; Weitkamp, J. Solvothermal Synthesis and Characterization of Large-Crystal All-Silica, Aluminum-, and Boron-Containing Ferrierite Zeolites. Chem. Mater. 2011, 23, 2521–2528. [Google Scholar] [CrossRef]
  96. Meng, X.; Nawaz, F.; Xiao, F.-S. Templating Route for Synthesizing Mesoporous Zeolites with Improved Catalytic Properties. Nano Today 2009, 4, 292–301. [Google Scholar] [CrossRef]
  97. Zhu, J.; Zhu, Y.; Zhu, L.; Rigutto, M.; van der Made, A.; Yang, C.; Pan, S.; Wang, L.; Zhu, L.; Jin, Y.; et al. Highly Mesoporous Single-Crystalline Zeolite Beta Synthesized Using a Nonsurfactant Cationic Polymer as a Dual-Function Template. J. Am. Chem. Soc. 2014, 136, 2503–2510. [Google Scholar] [CrossRef] [PubMed]
  98. Gu, F.N.; Wei, F.; Yang, J.Y.; Lin, N.; Lin, W.G.; Wang, Y.; Zhu, J.H. New Strategy to Synthesis of Hierarchical Mesoporous Zeolites. Chem. Mater. 2010, 22, 2442–2450. [Google Scholar] [CrossRef]
  99. Corma, A. From Microporous to Mesoporous Molecular Sieve Materials and Their Use in Catalysis. Chem. Rev. 1997, 97, 2373–2420. [Google Scholar] [CrossRef] [PubMed]
  100. Kresge, C.T.; Leonowicz, M.E.; Roth, W.J.; Vartuli, J.C.; Beck, J.S. Ordered Mesoporous Molecular Sieves Synthesized by a Liquid-Crystal Template Mechanism. Nature 1992, 359, 710–712. [Google Scholar] [CrossRef]
  101. Catizzone, E.; Migliori, M.; Aloise, A.; Lamberti, R.; Giordano, G. Hierarchical Low Si/Al Ratio Ferrierite Zeolite by Sequential Postsynthesis Treatment: Catalytic Assessment in Dehydration Reaction of Methanol. J. Chem. 2019, 2019, 3084356. [Google Scholar] [CrossRef] [Green Version]
  102. Cheng, X.; Cacciaguerra, T.; Minoux, D.; Dath, J.-P.; Fajula, F.; Gérardin, C. Generation of Parallelepiped-Shaped Mesopores and Structure Transformation in Highly Stable Ferrierite Zeolite Crystals by Framework Desilication in NaOH Solution. Microporous Mesoporous Mater. 2018, 260, 132–145. [Google Scholar] [CrossRef]
  103. Khitev Yu, P.; Kolyagin Yu, G.; Ivanova, I.I.; Ponomareva, O.A.; Thibault-Starzyk, F.; Gilson, J.-P.; Fernandez, C.; Fajula, F. Synthesis and Catalytic Properties of Hierarchical Micro/Mesoporous Materials Based on FER Zeolite. Microporous Mesoporous Mater. 2011, 146, 201–207. [Google Scholar] [CrossRef]
  104. Pan, S.; Wu, Q.; Wang, X.; Chen, F.; Meng, X.; Xiao, F.-S. Mesoporous EU-1 Zeolite Synthesized in the Presence of Cationic Polymer. Microporous Mesoporous Mater. 2016, 235, 246–252. [Google Scholar] [CrossRef]
  105. Xu, H.; Lei, C.; Wu, Q.; Zhu, Q.; Meng, X.; Dai, D.; Maurer, S.; Parvulescu, A.-N.; Müller, U.; Xiao, F. Organosilane Surfactant-Assisted Synthesis of Mesoporous SSZ-39 Zeolite with Enhanced Catalytic Performance in the Methanol-to-Olefins Reaction. Front. Chem. Sci. Eng. 2020, 14, 267–274. [Google Scholar] [CrossRef]
  106. Wu, L.; Degirmenci, V.; Magusin, P.C.M.M.; Szyja, B.M.; Hensen, E.J.M. Dual Template Synthesis of a Highly Mesoporous SSZ-13 Zeolite with Improved Stability in the Methanol-to-Olefins Reaction. Chem. Commun. 2012, 48, 9492. [Google Scholar] [CrossRef] [PubMed]
  107. Sulikowski, B.; Klinowski, J. Synthesis of a Novel Gallosilicate with the Ferrierite Structure. J. Chem. Soc. Chem. Commun. 1989, 1289. [Google Scholar] [CrossRef]
  108. Borade, R.B.; Clearfield, A. Synthesis of an Iron Silicate with the Ferrierite Structure. Chem. Commun. 1996, 2267. [Google Scholar] [CrossRef]
  109. Shevade, S.; Ahedi, R.K.; Kotasthane, A.N. Synthesis and Characterization of Ferrisilicate Analogs of Ferrierite (Fe-FER) Zeolites. Catal. Lett. 1997, 49, 69–75. [Google Scholar] [CrossRef]
  110. Zhao, G.; Benhelal, E.; Adesina, A.; Kennedy, E.; Stockenhuber, M. Comparison of Direct, Selective Oxidation of Methane by N2O over Fe-ZSM-5, Fe-Beta, and Fe-FER Catalysts. J. Phys. Chem. C 2019, 123, 27436–27447. [Google Scholar] [CrossRef]
  111. Ahedi, R.K.; Kotasthane, A.N. Synthesis of FER Titanosilicates from a Non-Aqueous Alkali-Free Seeded System. J. Mater. Chem. 1998, 8, 1685–1686. [Google Scholar] [CrossRef]
  112. Shevade, S.S.; Rao, B.S. Synthesis of a Vanadium Analog of Siliceous FER. J. Mater. Chem. 1999, 9, 2459–2462. [Google Scholar] [CrossRef]
  113. Corma, A.; Diaz, U.; Domine, M.E.; Fornés, V. Ti-Ferrierite and TiITQ-6: Synthesis and Catalytic Activity for the Epoxidation of Olefins with H2O2. Chem. Commun. 2000, 137–138. [Google Scholar] [CrossRef]
Molecules 25 03722 g001 550
Figure 1. Schematic diagram of special autoclave for the vapor-phase transport synthesis: (a) thermocouple, (b) agitator, (c) Teflon vessel, (d) support, (e) perforated plate, (f) amorphous gel and (g) liquid phase. Reprinted with permission from ref. [28]. Copyright 1996, Elsevier.
Figure 1. Schematic diagram of special autoclave for the vapor-phase transport synthesis: (a) thermocouple, (b) agitator, (c) Teflon vessel, (d) support, (e) perforated plate, (f) amorphous gel and (g) liquid phase. Reprinted with permission from ref. [28]. Copyright 1996, Elsevier.
Molecules 25 03722 g001
Molecules 25 03722 g002 550
Figure 2. Schematic representation of the self-assembly of tetramethylammonium (TMA)-filled cavities around benzylmethylpyrrolidinium (BMP) molecules to give the final FER structure. Reprinted with permission from ref. [66]. Copyright 2007, American Chemical Society.
Figure 2. Schematic representation of the self-assembly of tetramethylammonium (TMA)-filled cavities around benzylmethylpyrrolidinium (BMP) molecules to give the final FER structure. Reprinted with permission from ref. [66]. Copyright 2007, American Chemical Society.
Molecules 25 03722 g002
Molecules 25 03722 g003 550
Figure 3. Temperature-dependent hyperpolarized 129Xe Nuclear Magnetic Resonance (NMR) spectra of Xe adsorbed in the obtained FER zeolite sample and the possible linkage between the structures of MCM-49 and FER. Reprinted with permission from ref. [87]. Copyright 2014, Elsevier.
Figure 3. Temperature-dependent hyperpolarized 129Xe Nuclear Magnetic Resonance (NMR) spectra of Xe adsorbed in the obtained FER zeolite sample and the possible linkage between the structures of MCM-49 and FER. Reprinted with permission from ref. [87]. Copyright 2014, Elsevier.
Molecules 25 03722 g003
Molecules 25 03722 g004 550
Figure 4. (A) TEM images of aluminosilicate FER zeolite nanocrystals synthesized with Si/Al molar ratios of 15 at (a) 150 °C and (b) 120 °C, respectively. (B) Catalytic performance including (a) 1-pentene conversion versus time on stream (TOS) and (b) selectivity within the C5+ liquid fraction in oligomerization of 1-pentene to liquid fuels reactions over aluminosilicate FER zeolite: R-FER (reference FER zeolite synthesized using Pi as a single OSDA), N-FER(15)-150 and N-FER(15)-120 (FER zeolite nanocrystals synthesized with Si/Al molar ratios of 15 at 150 °C and 120 °C). Reprinted with permission from ref. [7]. Copyright 2018, Wiley.
Figure 4. (A) TEM images of aluminosilicate FER zeolite nanocrystals synthesized with Si/Al molar ratios of 15 at (a) 150 °C and (b) 120 °C, respectively. (B) Catalytic performance including (a) 1-pentene conversion versus time on stream (TOS) and (b) selectivity within the C5+ liquid fraction in oligomerization of 1-pentene to liquid fuels reactions over aluminosilicate FER zeolite: R-FER (reference FER zeolite synthesized using Pi as a single OSDA), N-FER(15)-150 and N-FER(15)-120 (FER zeolite nanocrystals synthesized with Si/Al molar ratios of 15 at 150 °C and 120 °C). Reprinted with permission from ref. [7]. Copyright 2018, Wiley.
Molecules 25 03722 g004
Molecules 25 03722 g005 550
Figure 5. (a) Dependence of adsorption energy on FER {100} surfaces on the number of DMPi molecules and its schematic diagram, (b) dependence of surface energy on FER {100} on the number of layers of the FER structure and its schematic diagram, (c,d) SEM images, (e–h) TEM images of the nanosheets of aluminosilicate FER zeolites and corresponding projections of the FER framework along (f) [010], (g) [0–11] and (h) [100], respectively. Reprinted with permission from ref. [61]. Copyright 2019, The Royal Society of Chemistry.
Figure 5. (a) Dependence of adsorption energy on FER {100} surfaces on the number of DMPi molecules and its schematic diagram, (b) dependence of surface energy on FER {100} on the number of layers of the FER structure and its schematic diagram, (c,d) SEM images, (e–h) TEM images of the nanosheets of aluminosilicate FER zeolites and corresponding projections of the FER framework along (f) [010], (g) [0–11] and (h) [100], respectively. Reprinted with permission from ref. [61]. Copyright 2019, The Royal Society of Chemistry.
Molecules 25 03722 g005
Molecules 25 03722 g006 550
Figure 6. (a1–c1) low-magnification and (a2–c2) high-magnification TEM images of FER zeolite samples synthesized with CTAB in NaOH solution with different NaOH concentration of (a) 0.05, (b) 0.25, and (c) 0.5 mol/L at 130 °C for 72 h, respectively. Reprinted with permission from ref. [102]. Copyright 2018, Elsevier.
Figure 6. (a1–c1) low-magnification and (a2–c2) high-magnification TEM images of FER zeolite samples synthesized with CTAB in NaOH solution with different NaOH concentration of (a) 0.05, (b) 0.25, and (c) 0.5 mol/L at 130 °C for 72 h, respectively. Reprinted with permission from ref. [102]. Copyright 2018, Elsevier.
Molecules 25 03722 g006
Molecules 25 03722 g007 550
Figure 7. (a) Methane conversion and (b) N2O conversion over the different catalysts at 350 °C (Fe-ZSM-5, Fe-Beta, Fe-FERa, 200 mg of catalysts; Fe-FERb, 100 mg of catalyst). Reprinted with permission from ref. [110]. Copyright 2019, American Chemical Society.
Figure 7. (a) Methane conversion and (b) N2O conversion over the different catalysts at 350 °C (Fe-ZSM-5, Fe-Beta, Fe-FERa, 200 mg of catalysts; Fe-FERb, 100 mg of catalyst). Reprinted with permission from ref. [110]. Copyright 2019, American Chemical Society.
Molecules 25 03722 g007
Table
Table 1. Distinguishable features of synthesis routes for the preparation of aluminosilicate ferrierite (FER) zeolite.
Table 1. Distinguishable features of synthesis routes for the preparation of aluminosilicate ferrierite (FER) zeolite.
EntrySynthesis RoutesFeaturesRef.
1Hydrothermal synthesiswater as a solvent[20,32,33,34,35]
2Solvothermal synthesisorganic molecules as the solvents [22,27]
3Vapor-phase transport (VPT)vapor containing a small amount of OSDA and water in the dry aluminosilicate gel[28,36]
4Transformation synthesisrecrystallization of zeolites with different topologies[29,37]
5Solid-transformation synthesislow water content and relatively high OSDA content[30]
6Microwave-assisted synthesisrapid synthesis with microwave as the energy source[31]
7Topotactic conversioncondensation of layered precursors[38,39,40,41]
Table
Table 2. Overview of the reported organic templates, their molecular structures and the corresponding synthesis methods.
Table 2. Overview of the reported organic templates, their molecular structures and the corresponding synthesis methods.
EntryOrganic TemplatesStructuresSynthesis Method 1Ref
1tetramethylammonium (TMA) Molecules 25 03722 i001HT[32]
2ethylenediamine (EDA) Molecules 25 03722 i002HT, VPT, SS[30,34,50]
3pyrrolidine (THP) Molecules 25 03722 i003HT[35,50,51,52,53]
4dibutylamine (DBA) Molecules 25 03722 i004ST[27]
5n-butylamine (n-BA) Molecules 25 03722 i005HT[54]
61,8-diaminooctane (DAO) Molecules 25 03722 i006HT[55]
7isopropylamine (IPA) Molecules 25 03722 i007HT[56]
8pyridine (Py) Molecules 25 03722 i008HT[57,58]
9piperidine (Pi) Molecules 25 03722 i009HT, SS,[6,29,37,59]
10tetrahydrofuran (THF) Molecules 25 03722 i010HT, VPT[26,36,60]
11N, N-diethyl-cis-2,6-dimethyl piperidinium (DMPi) Molecules 25 03722 i011HT[18,61]
121,3-dimethyimidazolium (DMI) Molecules 25 03722 i012SS[62,63]
13ethylene glycol (EG) Molecules 25 03722 i013HT[64,65]
14benzylmethylpyrrolidinium (BMP) Molecules 25 03722 i014HT (combined with TMA)[66]
15hexamethyleneimine (HMI) Molecules 25 03722 i015HT (combined with TMA)[68]
161,4-diazabicyclo [2.2.2] octane (DAB) Molecules 25 03722 i016HT (combined with TMA)[68]
171,6-bis (N-methylpyrrolidinium)hexane (MPH) Molecules 25 03722 i017HT (combined with TMA)[69]
1 HT: hydrothermal synthesis, SS: solid-state synthesis, VPT: vapor-phase transport synthesis, ST: solvothermal synthesis.
Table
Table 3. Detailed information of heteroatomic FER zeolites.
Table 3. Detailed information of heteroatomic FER zeolites.
EntryHeteroatomic FER ZeolitesSi/Heteroatom RatioRef.
1B-FERNot mentioned[19]
2Si, Ga-FERSi/Ga = 6.6[107]
3Fe-FERSi/Fe = 16[8]
Si/Fe = 11[108]
Si/Fe = 15–100[109]
Si/Fe = 38[110]
4Ti-FERSi/Ti = 83–182[111]
Not mentioned[113]
5V-FERSi/V = 120, 180[112]

Share and Cite

MDPI and ACS Style

Xu, H.; Zhu, J.; Zhu, L.; Zhou, E.; Shen, C. Advances in the Synthesis of Ferrierite Zeolite. Molecules 2020, 25, 3722. https://doi.org/10.3390/molecules25163722

AMA Style

Xu H, Zhu J, Zhu L, Zhou E, Shen C. Advances in the Synthesis of Ferrierite Zeolite. Molecules. 2020; 25(16):3722. https://doi.org/10.3390/molecules25163722

Chicago/Turabian Style

Xu, Hao, Jie Zhu, Longfeng Zhu, Enmu Zhou, and Chao Shen. 2020. "Advances in the Synthesis of Ferrierite Zeolite" Molecules 25, no. 16: 3722. https://doi.org/10.3390/molecules25163722

APA Style

Xu, H., Zhu, J., Zhu, L., Zhou, E., & Shen, C. (2020). Advances in the Synthesis of Ferrierite Zeolite. Molecules, 25(16), 3722. https://doi.org/10.3390/molecules25163722

Article Metrics

Back to TopTop