Analysis of Thermodynamic Properties for Rare Earth Complexes in Ionic Liquids by Raman Spectroscopy and DFT Calculation

The coordination states of the divalent and trivalent rare earth complexes in ionic liquid, triethyl-pentyl-phosphonium bis(trifluoromethyl-sulfonyl) amide [P2225][TFSA] were investigated by Raman spectroscopy and DFT calculation. The concentration dependences of the deconvoluted Raman spectra were investigated for 0.23-0.45 mol kg-1 RE(III), RE=Nd and Dy, and the mixed sample of RE(II)/RE(III)=1/3 at the molar ratio in [P2225][TFSA]. According to the conventional analysis, the solvation number; n of rare earth complexes in [P2225][TFSA] were determined to be n=4.06 for Nd(II), 5.01 for Nd(III), 4.12 for Dy(II) and 5.00 for Dy(III). Thermodynamic properties such as ΔisoG, ΔisoH and ΔisoS for the isomerism of [TFSA]- from trans- to cis-isomer in bulk and the first solvation sphere of the centered [RE3+] cation in [P2225][TFSA] were evaluated from the temperature dependence in the range of 298-398K. ΔisoG(bulk), ΔisoH(bulk) and TΔisoS(bulk) at 298 K were -1.06, 6.86, and 7.92 kJ mol-1, respectively. The trans-[TFSA]-was dominant in the enthalpy due to the positive value of ΔisoH(bulk) and TΔisoS(bulk) was slightly larger than ΔisoH(bulk), so that cis-[TFSA]- was revealed to be an entropy-controlled in [P2225][TFSA]. On the other hand, in the first solvation sphere of [RE3+] cation, ΔisoH (Nd)(-47.39 kJ mol-1) increased to the negative value remarkably and implied that the cis-[TFSA]- isomers were stabilized for enthalpy. ΔisoH(Nd) contributed to the remarkable decrease in the ΔisoG(Nd) and this result clearly indicated that the cis-[TFSA]- bound to Nd3+ cation was preferred and the coordination state of [Dy(III)(cis-TFSA)5]2- was stable in [P2225][TFSA] The optimized geometries and the bonding energies of [RE(II)(cis-TFSA)4]2- and [RE(III)(cis-TFSA)5]2- clusters were also investigated from DFT calculation with ADF package. The bonding energy; ΔEb was calculated from ΔEb= Etot(cluster) - Etot(RE2,3+) - nEtot([TFSA]-). ΔEb([Nd(II)(cis-TFSA)4]2-), ΔEb([Nd(III)(cis-TFSA)5]2-), ΔEb([Dy(II)(cis-TFSA)4]2-) and ΔEb([Dy(III)(cis-TFSA)5]2-) were -2241.6, -4362.3, -2135.4 and -4284.2 kJmol-1, respectively. This result was revealed that [RE(III)(cis-TFSA)5]2-cluster formed stronger coordination bonds than [Dy(II)(cis-TFSA)4]2- cluster. The average atomic charges and the bond distances of these clusters were consistent with the thermodynamic properties

Phase equilibrium relations of tetra-n-butylphosphonium propionate and butyrate semiclathrate hydrates

This paper reports phase equilibrium (temperature–composition) relations of semiclathrate hydrates formed from tetra-n-butylphosphonium propionate (TBP-Pro) and butyrate (TBP-But) + water systems. Their maximum solid–liquid phase equilibrium temperatures at atmospheric pressure were located at (288.75 ± 0.06) K and the mole fraction x1 = 0.035 ± 0.001 and (287.01 ± 0.06) K and x1 = 0.028 ± 0.001, respectively. They showed equilibrium temperatures higher than those of tetra-n-butylphosphonium formate, acetate, and lactate semiclathrate hydrates. The dissociation enthalpies of TBP-Pro and TBP-But semiclathrate hydrates were (190 ± 5) J·g−1 and (204 ± 5) J·g−1, respectively. The temperature difference between formation and dissociation, that is, the maximum allowable degree of supercooling, was (17.7 ± 1.5) K for TBP-Pro semiclathrate hydrate and (15.4 ± 1.4) K for TBP-But one

Phase equilibrium relations for tetra-n-butylphosphonium acetate semiclathrate hydrate systems in the presence of methane, carbon dioxide, nitrogen, or ethane

Thermodynamic stabilities of tetra-n-butylphosphonium acetate (TBP-Ace) semiclathrate hydrates in the presence of methane (CH 4 ), carbon dioxide (CO 2 ), nitrogen (N 2 ), or ethane (C 2 H 6 ) were measured in a pressure range up to approximately 5 MPa. The dissociation temperature of TBP-Ace + CH 4 , TBP-Ace + CO 2 , and TBP-Ace + N 2 semiclathrate hydrates increased drastically with an increase in pressure, which means that CH 4 , CO 2 , and N 2 molecules occupy the vacant cages of the TBP-Ace semiclathrate hydrate. On the other hand, the C 2 H 6 molecules hardly occupied the cages, resulting in small pressure dependence of the dissociation temperature. Raman spectra and powder X-ray diffraction patterns of TBP-Ace + CO 2 semiclathrate hydrate reveal that the phase transition occurs at 1.04 ± 0.04 MPa and 285.88 ± 0.05 K. One of the possible reasons why the phase transition occurs is that the carbonate and/or hydrogen carbonate anions derived from the CO 2 molecules are replaced with some of acetate anions in the TBP-Ace + CO 2 semiclathrate hydrate

Phase equilibrium temperature and dissociation enthalpy in the tri-n-butylalkylphosphonium bromide semiclathrate hydrate systems

Semiclathrate hydrate (SCH) is one of the phase change materials suitable for cold storage. The thermodynamic properties of SCHs, such as an equilibrium temperature and a dissociation enthalpy, depend on the size and shape of guest substances. In this study, to reveal the effect of cation size and shape on the thermodynamic properties, tri-n-butylalkylphosphonium bromide (P444R-Br) SCHs, where the alkyl group was n-propyl (R = 3), n-butyl (R = 4), n-pentyl (R = 5), i-butyl (R = i-4), i-pentyl (R = i-5), or allyl (R = Al)), were investigated. The branched alkyl groups (R = i-4 or i-5) raised the equilibrium temperature, whereas the shorter alkyl groups (R = 3 or Al) lowered one. Except for P4445-Br and P444(Al)-Br SCHs, the other P444R-Br SCHs had the same orthorhombic structure. Among the orthorhombic systems in the present study, the semiclathrate hydrate with a higher equilibrium temperature had a larger dissociation enthalpy

Thermodynamic Properties of Tetra-n-butylphosphonium Dicarboxylate Semiclathrate Hydrates

Semiclathrate hydrate (SCH) is one of the phase change materials suitable for cold energy storage. Thermodynamic properties of SCHs, such as an equilibrium temperature and the dissociation enthalpy, depend on the size and shape of the guest substances. In the present study, to reveal the effects of steric conformations of the guest anions on the thermodynamic properties of SCHs, tetra-n-butylphosphonium dicarboxylate (TBP-DC) SCHs, where the anion was oxalate (TBP-Oxa), malonate (TBP-Mal), succinate (TBP-Suc), glutarate (TBP-Glu), maleate (TBP-Male), or fumarate (TBP-Fum), were investigated. TBP-Oxa, -Mal, -Suc, and -Fum SCHs had similar equilibrium temperatures, whereas the equilibrium temperatures of TBP-Glu and -Male SCHs were higher. This suggests that the size and conformation of glutarate and maleate anions are appropriate for the cage structures of SCHs. Moreover, we compared the equilibrium temperatures of TBP-Suc, -Male, and -Fum SCHs because TBP-Suc, -Male, and -Fum have similar anion structures. The equilibrium temperature of TBP-Suc SCH was similar to that of TBP-Fum SCH, whereas TBP-Male SCH showed a higher equilibrium temperature. This result implies that the succinate anion is accommodated in the trans conformation, similar to the fumarate anion, in the hydrate cages.Jin Shimada, Moe Yamada, Atsushi Tani et al. Thermodynamic Properties of Tetra-n-butylphosphonium Dicarboxylate Semiclathrate Hydrates. Journal of Chemical & Engineering Data, 67 (1), 67-73, January 13, © 2022 American Chemical Society. https://doi.org/10.1021/acs.jced.1c0074

Phase Equilibrium Relations of Semiclathrate Hydrates Based on Tetra- n-butylphosphonium Formate, Acetate, and Lactate

Phase equilibrium (temperature-composition) relations of tetra-n-butylphosphonium formate (TBP-For), acetate (TBP-Ace), and lactate (TBP-Lac) semiclathrate hydrate systems have been measured. The highest equilibrium temperatures of TBP-For, TBP-Ace, and TBP-Lac semiclathrate hydrates were 280.9, 284.6, and 283.8 K at the atmospheric pressure, respectively, where the composition of tetra-n-butylphosphonium carboxylate was approximately 0.035 ± 0.001 (mole fraction) in every system. The dissociation enthalpies of tetra-n-butylphosphonium carboxylate semiclathrate hydrates were measured by differential scanning calorimetry. The dissociation enthalpies of TBP-For, TBP-Ace, and TBP-Lac semiclathrate hydrates were (187 ± 3), (193 ± 3), and (177 ± 3) J·g-1, respectively.Jin Shimada, Masami Shimada, Takeshi Sugahara, et al. Phase Equilibrium Relations of Semiclathrate Hydrates Based on Tetra-n-butylphosphonium Formate, Acetate, and Lactate. Journal of Chemical & Engineering Data, 63 (9), 3615-3620, September 13, © 2018 American Chemical Society. https://doi.org/10.1021/acs.jced.8b0048

Ion transport and structural dynamics in homologous ammonium and phosphoniumbased room temperature ionic liquids

Charge transport and structural dynamics in a homologous pair of ammonium and phosphonium based room temperature ionic liquids (ILs) have been characterized over a wide temperature range using broadband dielectric spectroscopy and quasi-elastic light scattering spectroscopy. We have found that the ionic conductivity of the phosphonium based IL is significantly enhanced relative to the ammonium homolog, and this increase is primarily a result of a lower glass transition temperature and higher ion mobility. Additionally, these ILs exhibit pronounced secondary relaxations which are strongly influenced by the atomic identity of the cation charge center. While the secondary relaxation in the phosphonium IL has the expected Arrhenius temperature dependence characteristic of local beta relaxations, the corresponding relaxation process in the ammonium IL was found to exhibit a mildly non-Arrhenius temperature dependence in the measured temperature range—indicative of molecular cooperativity. These differences in both local and long-range molecular dynamics are a direct reflection of the subtly different inter-ionic interactions and mesoscale structures found in these homologous ILs