NR  Vol.12 No.3 , March 2021
Synthesis and Characterization of Methanesulfonate and Ethanesulfonate Intercalated Lithium Aluminum LDHs
Abstract: LDH-phases become increasingly interesting due to their broad ability to be able to incorporate many different cations and anions. The intercalation of methanesulfonate and ethanesulfonate into a Li-LDH as well as the behavior of the interlayer structure as a function of the temperature is presented. A hexagonal P63/m [LiAl2(OH)6][Cl?1.5H2O] (Li-Al-Cl) precursor LDH was synthesized by hydrothermal treating of a LiCl solution with γ-Al(OH)3. This precursor was used to intercalate methanesulfonate (CH3O3S?) and ethanesulfonate (C2H5O3S?) through anion exchange by stirring Li-Al-Cl in a solution of the respective organic Li-salt (90?C, 12 h). X-ray diffraction pattern showed an increase of the interlayer space c' (d001) of Li-Al-methanesulfonate (Li-Al-MS) with 1.2886 nm and Li-Al-ethanesulfonate (Li-Al-ES) with 1.3816 nm compared to the precursor with 0.7630 nm. Further investigations with Fourier-transform infrared spectroscopy and scanning electron microscopy confirmed a complete anion exchange of the organic molecules with the precursor Cl?. Both synthesized LDH compounds [LiAl2(OH)6]CH3SO3?nH2O (n = 2.24-3.72 (Li-Al-MS) and [LiAl2(OH)6]C2H5SO3}?nH2O (n = 1.5) (Li-Al-ES) showed a monomolecular interlayer structure with additional interlayer water at room temperature. By increasing the temperature, the interlayer water was removed and the interlayer space c' of Li-Al-MS decreased to 0.87735 nm (at 55?C). Calculations showed that a slight displacement of the organic molecules is necessary to achieve this interlayer space. Different behavior of Li-Al-ES could be observed during thermal treatment. Two phases coexisted at 75?C - 85?C, one with a reduced c' (0.9015 nm, 75?C) and one with increased c' (1.5643 nm, 85?C) compared to the LDH compound at room temperature. The increase of c' is due to the formation of a bimolecular interlayer structure.

1. Introduction

Layered double hydroxides (LDHs) consist of alternate positively charged mixed metal hydroxide layers and negatively charged interlayer anions and can be normally described by the formula:

[ M 1 x z + M x 3 + ( OH ) 2 ] p + [ ( A n ) p / n mH 2 O ]

with z = 2, M = bi- and trivalent metallic elements, A = organic or inorganic anions and m = amount of interlayer H2O depending on the relative humidity, hydration level and temperature [1] [2]. The ratio of M2+ to M3+ can be variable [3]. Unlike other LDHs, lithium-containing LDHs are based on the Al(OH)3 structure with a solid cation ratio of 1:2 (Li:Al). The Al(OH)3 structure is built up of double-layered sheets of hexagonally packed O atoms. Two-thirds of the octahedral holes are occupied by Al Atoms. During a LDH synthesis with LiX (X = Cl, OH, NO 3 , etc.), the remaining third will be occupied by Li Atoms which will lead to the 1:2 ratio [1] [4] [5] [6] [7].

The positive charged main layer must be compensated by a negative charge. This is achieved by the intercalation of anions in the interlayer. These can be both inorganic (e.g. CO 3 2 , Cl) and organic (e.g. CH3O3S) anions [1] [8] [9] [10] [11]. The interlayer space depends on the type and size respectively chain length and the orientation of the intercalated anion [12]. In the present study, the successful synthesis of Li-Al-LDHs with intercalated methanesulfonate (CH3O3S) and ethanesulfonate (C2H5O3S) anions as well as the possible interlayer structure as a function of the temperature is reported. These typical intercalation reactions of LDH-phases and their varying interlayer arrangements are of high interest of layered structures of LDH-type with a main layered metal of ion charge (+1), and the varying compositions and probable applications of these different intercalated LDH phases.

2. Experimental and Analytical Work

2.1. Reagents

The materials used within this work were LiCl (Roth, purity ≥ 99%), γ-Al(OH)3 (Merck, purity ≥ 98%), LiOH (AppliChem, purity ≥ 99%), CH4O3S (Lancaster, purity ≥ 98%) and C2H6O3S (Merck, purity ≥ 98%). All chemicals tested by powder X-ray diffraction (PXRD), Fourier-transform infrared spectroscopy (FT-IR) and thermogravimetric analysis (TGA) for purity and loss on ignition (LOI). As methanesulfonic acid and ethanesulfonic acid are in liquid state at room temperature, they were neutralized by LiOH and transformed into solid lithium salts prior to the use in the investigations.

2.2. Methods

For PXRD investigations at room temperature, a PANalytical X’PERT3 Powder diffractometer with a Pixcel detector and Cu radiation (45 kV/40 mA) was used. Approximately 1 g of the respective sample was prepared in a standard sample holder by back loading procedure and recorded from 4˚ - 70˚2θ with a step width of 0.013˚2θ and the irradiation time of 20.41 s per step. High temperature PXRD between 25˚C and 400˚C were performed by a PANalytical X’PERT Pro MPD (Cu, 45 kV/40 mA) with an Anton-Paar high temperature chamber and a X’Celerator detector. The respective sample was prepared on a platinum band and recorded from 2˚ - 50˚2θ with a step width of 0.0167˚2θ and an irradiation time of 19.69 s. To record the LOI and determine the type of the vaporized molecule, thermogravimetric analysis with parallel differential scanning calorimetry (TGA/DSC) and coupled mass spectrometer (MS) were performed using a NETZSCH STA449 F3 Jupiter and a NETZSCH QMS 403 D Aëolos. The samples were heated up from 25˚C to 1000˚C with a heating rate of 10˚C/min within an Argon atmosphere. The chemical composition and the 1:2 ratios between Li and Al of the main layer were proofed using a Horiba Ultima 2 inductively coupled plasma optical emission spectroscopy (ICP-OES). FT-IR spectra were recorded with a Bruker Tensor II spectrometer (400 - 4000 cm−1) to verify the complete anion exchange and the intercalation of the organic molecules. Sample pictures were taken by a JOEL 640 scanning electron microscope (SEM). In addition, energy dispersive X-ray spectroscopy (EDX) was performed to detect a possible remainder of precursor Cl.

2.3. Synthesis

Methanesulfonic acid and ethanesulfonic acid were used in the reaction to the newly formed Li-salts by neutralizing the respective acid with LiOH until a pH of 7 - 7.5 was reached. The LDH [LiAL2(OH)6][Cl·0.5H2O] (Li-Al-Cl) was selected as the precursor due to the easy interchangeability of the Cl anion [13] and synthesized by a variation of the hydrothermal method [13] [14]. A good crystalline precursor was achieved by adding 1 g of γ-Al(OH)3 to 15 ml of a LiCl solution with a few drops of 0.5 mole LiOH (pH 8 - 8.5). The educt ratio of Al:Li was 1:5 [15] [16]. The suspension was heated to 100˚C for 10 hours in an autoclave. After completion of the synthesis the product was filtered, washed with 50 ml deionized H2O, dried to a relative humidity (RH) of 35% and analyzed for purity and amount of crystal water. To exchange Cl for methanesulfonate or ethanesulfonate, 1 g of the precursor was added to 25 ml deionized H2O and so much of the respective Li-salt was added that a ratio of Cl:X (X = organic anion) of 1:2 was obtained. The suspensions were heated up to 90˚C for 12 h under constant stirring. After completion of the synthesis, the products were filtered, washed with 50 ml deionized H2O and dried to 35% RH. The entire synthesis processes were performed in a glove box with N2 atmosphere to avoid carbonization.

3. Results and Discussion

3.1. TGA/DSC-MS and ICP-OES Analysis

Exactly 10 mg of the respective LDH were dissolved in 0.5 ml suprapure 65% HNO3, diluted with 10 ml deionized H2O and measured with ICP-OES. The results showed the expected Li/Al ratio of 1:2 and no leftover of Cl from the precursor. The amount of interlayer water and the amount of the absorbed organic molecule was determined by TGA/DTA-MS with approximately 10 mg of the respective LDH. The mass losses can be divided in three steps for both sulfonate containing LDHs. The interlayer water is removed between 25˚C and 200˚C with a total of 2.24 mol H2O for Li-Al-methanesulfonate (Li-Al-MS) and 3.72 mol H2O for Li-Al-ethanesulfonate (Li-Al-ES). The decomposition of the main layer starts at approx. 250˚C and continues to 295˚C. By removing the OH groups of the main layer at these elevated temperatures, the crystal structure is destroyed and the LDH compounds become X-ray amorphous. The last large mass loss lies between 400˚C and 500˚C and is caused by the breakdown of the organic compounds. Due to the mass spectroscopy, it was possible to differentiate between H2O and the organic molecules, which could be measured as fragments in the form of e.g. CH+ or SO2+. The chemical composition of both LDH compounds were therefore calculated (Table 1).

3.2. FT-IR Spectroscopy

Li-Al-MS and Li-Al-ES were investigated by FT-IR to proof the intercalation of the organic molecules and the noncarbonization of the relevant synthesis products. Both sulfonate LDHs showed the typical SO 3 2 (ν 1055 cm−1, νas 1202 cm−1, ν3 1242 cm−1, νas 1292 cm−1), CH3 (δs 1373 cm−1), H2O (ν2 1627 cm−1), OH (ν 3400 - 3600 cm−1) and Al-OH (δ 752 cm−1, δ 940 cm−1) absorptions. Li-Al-ethanesulfonate showed also the CH2 (δs 1417 cm−1, νas 2941 cm−1) absorptions of the methylene group [6] [17] [18] [19] [20]. No CO2/ CO 3 2 absorptions and therefore no carbonization of the compounds could be detected [6] [21].

3.3. SEM (EDX) Analysis

The investigated samples were free of Cl from the initial chemicals which proofed the complete anion exchange between the precursor and the sulfonate anions. Both LDHs formed flat hexagonal crystals with a clearly visible layered structure in crystallographic c-direction (Figure 1). The crystals of Li-Al-MS had an average size of 2 - 20 µm in crystallographic a-direction and 2 µm - 10 µm in crystallographic c-direction. In comparison, the crystals of Li-Al-ES were mostly smaller in the a-direction (1 - 10 µm) and showed strongly rounded crystal edges. These small crystals formed hexagonal clusters with layer thicknesses of up to 30 µm in c-direction.

Table 1. Calculated and measured compositions (mass %) of Li-Al-MS and Li-Al-ES (35% RH).

Figure 1. SEM pictures of (a) Li-Al-MS, (b) Li-Al-ES.

3.4. PXRD Analysis at 25˚C

The distance between two layers within the LDH structure can be described by the layer distance c' (d001) and depends on the type, size and inclination angle of the intercalated anion. This inclination angle α can be calculated by using the average increase of c' depending on the chain length (Δc'). Ethanesulfonate molecule is larger and therefore (requires more space in the interlayer, which leads to an increase in the interlayer distance c'. Table 2, Figure 2).

With the calculated Δc' = 0.0928 and the given formula sinα = Δc'/0.127, the inclination angle of the intercalated molecules is α = 46.95˚ (35% RH) [9].

A Li-Al-LDH layer with intercalated sulfonate anions is normally composed of the positively charged main layer with 0.20 nm between the OH groups and 0.29 nm between the OH and the SO 3 2 group (Figure 3). The terminal methyl group of the organic anions occupies 0.30 nm and the H2O molecules 0.31 nm of the interlayer space. The occupied space by the remaining part of organic anion can be calculated with the formula: 0.127 nm·(nc – 1)·sinα with nc = number of carbon atoms [9]. Based on these data the interlayer space for both LDH compounds could be calculated (Table 3).

With only one layer of H2O molecules, the differences between the measured and calculated interlayer spaces are too high. By adding mathematically another half layer of H2O molecules within the calculation (0.47 nm instead of 0.31 nm),

Table 2. Lattice parameters and amount of interlayer water of Li-Al-Ms and Li-Al-ES.

Table 3. Calculated and measured interlayer space c' of Li-Al-MS and Li-Al-ES with 1 and 1.5 layer of interlayer H2O and an inclination angle of 46.95˚.

Figure 2. XRD pattern of (a) Li-Al-ES, (b) Li-Al-MS with a shift of Li-Al-ES towards smaller ˚2theta due to the interlayer anion ethanesulfonate.

Figure 3. Example for the structure of a Li-Al-ES with an ethanesulfonate anion and 1.5 layers of H2O molecules (modified according to [9] ).

the difference could be calculated and adjusted. It can therefore be assumed, that the H2O molecules within the interlayer are offset by the half length in c-direction to each other (Figure 3).

While Li-Al-MS crystallized in the hexagonal space group P63/m, the space group of Li-Al-ES could be determined as monoclinic P21/c. The lattice parameters were determined by Pawley fit based on a 2H Li-Al unit cell [15].

3.5. PXRD Analysis at Higher Temperatures

The behavior of the LDH phases as a function of temperature was investigated by heating the phases up to 400˚C. Pure Si was added as standard to the samples to compensate the platinum band expansion and zero shifts.

Li-Al-MS showed a decrease of the lattice parameter c' starting at 45˚C - 55˚C from the original 1.2286 nm to 0.9873 nm followed by a second decrease at 55˚C - 65˚C to 0.8773 nm were the interlayer space remained nearly constant until the decomposition of the main layer at 295˚C with c' = 0.8831 nm (Figure 4, Table 4). The space group P63/m did not change at higher temperatures. Without interlayer H2O at temperatures above 200˚C the calculated interlayer space of Li-Al-MS is 0.79 nm. The difference of 0.0931 nm between the calculated and the measured c' (295˚C) can be explained by a slightly shift of the sulfonate molecules to each other at higher temperatures (Figure 5) [19] [22]. Both phases become X-Ray amorphous at about 300˚C due to the beginning destruction of main layer.

With a splitting in two different phases at 75˚C - 85˚C, Li-Al-ES did not show the same behavior. The interlayer spaces c' of the two phases are 0.9042 nm and 1.5643 nm at 85˚C. Assuming that the sulfonate anions can behave the same way

Figure 4. Shifts of lattice parameters c' depending on the temperature of (a) Li-Al-MS and (b) Li-Al-ES.

Table 4. Lattice distances c' of Li-Al-MS and Li-Al-ES depending on the temperature.

Figure 5. Interlayer structure of Li-Al-MS with a displacement of the methanesulfonate molecules for x nm in c-direction.

like aliphatic and aromatic monocarboxylic acids it is possible to form a “double” interlayer structure by placing two sulfonate anions above each other with an inclination angle of 90˚ (Figure 6). A doubled interlayer structure with α = 90˚ and without interlayer H2O (due to the high temperature) has a calculated interlayer space of 1.5840 nm which fits extremely good with the measured c' of the “higher spaced” phase (Table 4). Using only one layer of sulfonate anions in the interlayer structure and α = 90 for the calculation results in c'calc = 0.9170 nm, which also fits precisely with the measured interlayer spaces (Table 4).

Li-Al-ethanesulfonate hydrate with the lower interlayer phase is therefore a coexisting single layer version of the phase with an “increased interlayer space”. No change of the monoclinic space group P21/c during the heating process could be found.

3.6. Infrared Spectroscopy

Li-Al-LDHs with intercalated methanesulfonate (Figure 7) and ethanesulfonate (Figure 8) were also investigated by IR-spectroscopy and their spectra and interpretations (Table 5 and Table 6) are reported.

Figure 6. Interlayer structure of Li-Al-ES with a double layer of the ethanesulfonate molecules and an inclination angle of 90˚.

Table 5. IR spectroscopic data of [LiAl2(OH)6]X {X = CH3SO3}·nH2O.

Figure 7. IR spectroscopy of [LiAl2(OH)6]X {X = CH3SO3}·nH2O.

Figure 8. IR spectroscopy of [LiAl2(OH)6]X {X = C2H5SO3}·nH2O.

Table 6. IR spectroscopic data of [LiAl2(OH)6]X {X = C2H5SO3}·nH2O.

The different vibrations of [LiAl2(OH)6]X {X = CH3SO3}·nH2O were interpreted in Table 5.

The different vibrations of [LiAl2(OH)6]X {X = C2H5SO3}·nH2O were interpreted in Table 6.

4. Conclusions

The synthesis of crystalline and pure Li-Al-LDHs with intercalated methanesulfonate and ethanesulfonate by the anion exchange method using a Li-Al-Cl precursor is easily possible.

The following compositions were determined:

1) Li-Al-MS (Methylsulfonate)

[LiAl2(OH)6]X {X = CH3SO3}·nH2O (n = 2.24-3.72)

2) Li-Al-ES (Ethylsulfonate)

[LiAl2(OH)6]X {X = C2H5SO3}·nH2O (n = 1.5)

Calculations showed that the organic molecules were intercalated not in a flat arrangement, but with an inclination angle of α = 46.95˚ at 25˚C. By increasing the temperature, the inclination angle changed to 90˚. Li-Al-ES also showed a complete change of a part of the interlayer structure by stacking two organic molecules on top of each other (bimolecular) at higher temperatures. The other part remained in an unstacked single layer structure (monomolecular). The coexistence of both phases could be explained by a new formed superstructure arrangement. While Li-Al-MS remains in a monomolecular structure, the displacement of the organic molecules may indicate an incomplete formation of a bimolecular structure. By changing the environmental temperature, the interlayer structure and distance can be controlled.


The work was carried out at the University of Halle/Saale. The great help of people in the laboratory is gratefully acknowledged.

Cite this paper: Niksch, A. and Pöllmann, H. (2021) Synthesis and Characterization of Methanesulfonate and Ethanesulfonate Intercalated Lithium Aluminum LDHs. Natural Resources, 12, 59-71. doi: 10.4236/nr.2021.123006.

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