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

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

Invasion and Interaction Determine Population Composition in an Open Evolving System

It is well-known that interactions between species determine the population composition in an ecosystem. Conventional studies have focused on fixed population structures to reveal how interactions shape population compositions. However, interaction structures are not fixed, but change over time due to invasions. Thus, invasion and interaction play an important role in shaping communities. Despite its importance, however, the interplay between invasion and interaction has not been well explored. Here, we investigate how invasion affects the population composition with interactions in open evolving systems considering generalized Lotka-Volterra-type dynamics. Our results show that the system has two distinct regimes. One is characterized by low diversity with abrupt changes of dominant species in time, appearing when the interaction between species is strong and invasion slowly occurs. On the other hand, frequent invasions can induce higher diversity with slow changes in abundances despite strong interactions. It is because invasion happens before the system reaches its equilibrium, which drags the system from its equilibrium all the time. All species have similar abundances in this regime, which implies that fast invasion induces regime shift. Therefore, whether invasion or interaction dominates determines the population composition.Comment: 15 pages (including supplementary material), 8 figures (4 figures in main, 4 figures in SI

The phytotoxin coronatine is a multifunctional component of the virulence armament of Pseudomonas syringae

Plant pathogens deploy an array of virulence factors to suppress host defense and promote pathogenicity. Numerous strains of Pseudomonas syringae produce the phytotoxin coronatine (COR). A major aspect of COR function is its ability to mimic a bioactive jasmonic acid (JA) conjugate and thus target the JA-receptor COR-insensitive 1 (COI1). Biological activities of COR include stimulation of JA-signaling and consequent suppression of SA-dependent defense through antagonistic crosstalk, antagonism of stomatal closure to allow bacterial entry into the interior of plant leaves, contribution to chlorotic symptoms in infected plants, and suppression of plant cell wall defense through perturbation of secondary metabolism. Here, we review the virulence function of COR, including updates on these established activities as well as more recent findings revealing COI1-independent activity of COR and shedding light on cooperative or redundant defense suppression between COR and type III effector proteins

Quasi-elastic neutron scattering studies on fast dynamics of water molecules in tetra-n-butylammonium bromide semiclathrate hydrate

The dynamics of the water molecules in tetra-n-butyl-d36-ammonium bromide semiclathrate hydrate were investigated by quasi-elastic neutron scattering (QENS). The QENS results clearly revealed afast reorientation motion of water molecules in the temperature range of 212–278 K. The mean jumpdistance of hydrogen atoms was within 1.5‒2.0 Å. The relaxation time of water reorientation wasestimated to be 100‒410 ps with activation energy of 10.2±5.8 kJ·mol-1. The activation energy wasin good agreement with the cleavage energy of hydrogen bonds. Such a short relaxation time ofwater reorientation is possibly due to strong interaction between a bromide anion and its surroundingwater molecules (similar to so-called negative hydration), which suggests a unique strategy fordesigning efficient, safe, and inexpensive proton conductors having the framework of semiclathratehydrates.Shimada Jin, Tani Atsushi, Yamada Takeshi, et al. "Quasi-elastic neutron scattering studies on fast dynamics of water molecules in tetra-n-butylammonium bromide semiclathrate hydrate", Applied Physics Letters 123, 50 (2023) https://doi.org/10.1063/5.0157560

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