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Journal articles on the topic 'Reentrant condensation'

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Author: Grafiati

Published: 10 March 2023

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1

Truzzolillo, Domenico, Simona Sennato, Stefano Sarti, Stefano Casciardi, Chiara Bazzoni, and Federico Bordi. "Overcharging and reentrant condensation of thermoresponsive ionic microgels." Soft Matter 14, no. 20 (2018): 4110–25. http://dx.doi.org/10.1039/c7sm02357j.

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We investigated the complexation of thermoresponsive anionic poly(N-isopropylacrylamide) (PNiPAM) microgels and cationic ε-polylysine chains. We show that the volume phase transition of the microgels triggers polyion adsorption and gives rise to a thermosensitive microgel overcharging and reentrant condensation.

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2

Nguyen, T. T., I. Rouzina, and B. I. Shklovskii. "Reentrant condensation of DNA induced by multivalent counterions." Journal of Chemical Physics 112, no. 5 (February 2000): 2562–68. http://dx.doi.org/10.1063/1.480819.

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3

Zhang, Fajun, Felix Roosen-Runge, Andrea Sauter, Marcell Wolf, Robert M. J. Jacobs, and Frank Schreiber. "Reentrant condensation, liquid–liquid phase separation and crystallization in protein solutions induced by multivalent metal ions." Pure and Applied Chemistry 86, no. 2 (February 1, 2014): 191–202. http://dx.doi.org/10.1515/pac-2014-5002.

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Abstract We briefly summarize the recent progress in tuning protein interactions as well as phase behavior in protein solutions using multivalent metal ions. We focus on the influence of control parameters and the mechanism of reentrant condensation, the metastable liquid–liquid phase separation and classical vs. non-classical pathways of protein crystallization.

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4

Daga, Bijoy. "Reentrant condensation transition in a two species driven diffusive system." Physica A: Statistical Mechanics and its Applications 477 (July 2017): 1–8. http://dx.doi.org/10.1016/j.physa.2017.02.021.

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5

Sennato, S., F. Bordi, C. Cametti, M. Diociaiuti, and P. Malaspina. "Charge patch attraction and reentrant condensation in DNA–liposome complexes." Biochimica et Biophysica Acta (BBA) - Biomembranes 1714, no. 1 (August 2005): 11–24. http://dx.doi.org/10.1016/j.bbamem.2005.06.004.

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6

Sennato, S., D. Truzzolillo, F. Bordi, and C. Cametti. "Effect of Temperature on the Reentrant Condensation in Polyelectrolyte−Liposome Complexation." Langmuir 24, no. 21 (November 4, 2008): 12181–88. http://dx.doi.org/10.1021/la8021563.

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7

Sennato, S., F. Bordi, and C. Cametti. "On the phase diagram of reentrant condensation in polyelectrolyte-liposome complexation." Journal of Chemical Physics 121, no. 10 (September 8, 2004): 4936–40. http://dx.doi.org/10.1063/1.1781112.

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8

Alshareedah, Ibraheem, and Priya R. Banerjee. "Sequence-Encoded Interactions Modulate Reentrant Liquid Condensation of Ribonucleoprotein-RNA Mixtures." Biophysical Journal 118, no. 3 (February 2020): 372a. http://dx.doi.org/10.1016/j.bpj.2019.11.2129.

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9

Lenton, Samuel, Stefan Hervø-Hansen, Anton M. Popov, Mark D. Tully, Mikael Lund, and Marie Skepö. "Impact of Arginine–Phosphate Interactions on the Reentrant Condensation of Disordered Proteins." Biomacromolecules 22, no. 4 (March 18, 2021): 1532–44. http://dx.doi.org/10.1021/acs.biomac.0c01765.

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10

Zhang, Minmin, and Serge G. Lemay. "Interaction of Anionic Bulk Nanobubbles with Cationic Liposomes: Evidence for Reentrant Condensation." Langmuir 35, no. 11 (February 27, 2019): 4146–51. http://dx.doi.org/10.1021/acs.langmuir.8b03927.

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11

Zhou, Jihan, Fuyou Ke, and Dehai Liang. "Kinetic Study on the Reentrant Condensation of Oligonucleotide in Trivalent Salt Solution." Journal of Physical Chemistry B 114, no. 43 (November 4, 2010): 13675–80. http://dx.doi.org/10.1021/jp1074187.

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12

Zhang, Fajun, Sophie Weggler, Michael J. Ziller, Luca Ianeselli, Benjamin S. Heck, Andreas Hildebrandt, Oliver Kohlbacher, Maximilian W. A. Skoda, Robert M. J. Jacobs, and Frank Schreiber. "Universality of protein reentrant condensation in solution induced by multivalent metal ions." Proteins: Structure, Function, and Bioinformatics 78, no. 16 (September 24, 2010): 3450–57. http://dx.doi.org/10.1002/prot.22852.

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13

Cheng, Chao, Jun-Li Jia, and Shi-Yong Ran. "Polyethylene glycol and divalent salt-induced DNA reentrant condensation revealed by single molecule measurements." Soft Matter 11, no. 19 (2015): 3927–35. http://dx.doi.org/10.1039/c5sm00619h.

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In this study, we investigated the DNA condensation induced by polyethylene glycol (PEG) with different molecular weights (PEG 600 and PEG 6000) in the presence of NaCl or MgCl₂ by using magnetic tweezers (MT) and atomic force microscopy (AFM).

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14

Ramos,, José Ésio Bessa, Renko de Vries, and João Ruggiero Neto. "DNA Ψ-Condensation and Reentrant Decondensation: Effect of the PEG Degree of Polymerization." Journal of Physical Chemistry B 109, no. 49 (December 2005): 23661–65. http://dx.doi.org/10.1021/jp0527103.

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15

Seo, Dongjin, Alex M. Schrader, Szu-Ying Chen, Yair Kaufman, Thomas R. Cristiani, Steven H. Page, Peter H. Koenig, Yonas Gizaw, Dong Woog Lee, and Jacob N. Israelachvili. "Rates of cavity filling by liquids." Proceedings of the National Academy of Sciences 115, no. 32 (July 19, 2018): 8070–75. http://dx.doi.org/10.1073/pnas.1804437115.

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Understanding the fundamental wetting behavior of liquids on surfaces with pores or cavities provides insights into the wetting phenomena associated with rough or patterned surfaces, such as skin and fabrics, as well as the development of everyday products such as ointments and paints, and industrial applications such as enhanced oil recovery and pitting during chemical mechanical polishing. We have studied, both experimentally and theoretically, the dynamics of the transitions from the unfilled/partially filled (Cassie–Baxter) wetting state to the fully filled (Wenzel) wetting state on intrinsically hydrophilic surfaces (intrinsic water contact angle <90°, where the Wenzel state is always the thermodynamically favorable state, while a temporary metastable Cassie–Baxter state can also exist) to determine the variables that control the rates of such transitions. We prepared silicon wafers with cylindrical cavities of different geometries and immersed them in bulk water. With bright-field and confocal fluorescence microscopy, we observed the details of, and the rates associated with, water penetration into the cavities from the bulk. We find that unconnected, reentrant cavities (i.e., cavities that open up below the surface) have the slowest cavity-filling rates, while connected or non-reentrant cavities undergo very rapid transitions. Using these unconnected, reentrant cavities, we identified the variables that affect cavity-filling rates: (i) the intrinsic contact angle, (ii) the concentration of dissolved air in the bulk water phase (i.e., aeration), (iii) the liquid volatility that determines the rate of capillary condensation inside the cavities, and (iv) the presence of surfactants.

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16

Nguyen, T. T., and B. I. Shklovskii. "Complexation of DNA with positive spheres: Phase diagram of charge inversion and reentrant condensation." Journal of Chemical Physics 115, no. 15 (October 15, 2001): 7298–308. http://dx.doi.org/10.1063/1.1402988.

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17

Bordi, F., C. Cametti, M. Diociaiuti, D. Gaudino, T. Gili, and S. Sennato. "Complexation of Anionic Polyelectrolytes with Cationic Liposomes: Evidence of Reentrant Condensation and Lipoplex Formation." Langmuir 20, no. 13 (June 2004): 5214–22. http://dx.doi.org/10.1021/la036006u.

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18

Panter, J. R., and H. Kusumaatmaja. "The impact of surface geometry, cavitation, and condensation on wetting transitions: posts and reentrant structures." Journal of Physics: Condensed Matter 29, no. 8 (January 16, 2017): 084001. http://dx.doi.org/10.1088/1361-648x/aa5380.

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19

Mamontov, Eugene, and Hugh O'Neill. "Reentrant condensation of lysozyme: Implications for studying dynamics of lysozyme in aqueous solutions of lithium chloride." Biopolymers 101, no. 6 (March 25, 2014): 624–29. http://dx.doi.org/10.1002/bip.22430.

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20

Alshareedah, Ibraheem, Taranpreet Kaur, Jason Ngo, Hannah Seppala, Liz-Audrey Djomnang Kounatse, Wei Wang, Mahdi Muhammad Moosa, and Priya R. Banerjee. "Interplay between Short-Range Attraction and Long-Range Repulsion Controls Reentrant Liquid Condensation of Ribonucleoprotein–RNA Complexes." Journal of the American Chemical Society 141, no. 37 (August 22, 2019): 14593–602. http://dx.doi.org/10.1021/jacs.9b03689.

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21

Roosen-Runge, Felix, Benjamin S. Heck, Fajun Zhang, Oliver Kohlbacher, and Frank Schreiber. "Interplay of pH and Binding of Multivalent Metal Ions: Charge Inversion and Reentrant Condensation in Protein Solutions." Journal of Physical Chemistry B 117, no. 18 (May 2013): 5777–87. http://dx.doi.org/10.1021/jp401874t.

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22

Hsiao, Pai-Yi. "Overcharging, Charge Inversion, and Reentrant Condensation: Using Highly Charged Polyelectrolytes in Tetravalent Salt Solutions as an Example of Study." Journal of Physical Chemistry B 112, no. 25 (June 2008): 7347–50. http://dx.doi.org/10.1021/jp800331b.

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23

Sennato, Simona, Edouard Chauveau, Stefano Casciardi, Federico Bordi, and Domenico Truzzolillo. "The Double-Faced Electrostatic Behavior of PNIPAm Microgels." Polymers 13, no. 7 (April 4, 2021): 1153. http://dx.doi.org/10.3390/polym13071153.

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PNIPAm microgels synthesized via free radical polymerization (FRP) are often considered as neutral colloids in aqueous media, although it is well known, since the pioneering works of Pelton and coworkers, that the vanishing electrophoretic mobility characterizing swollen microgels largely increases above the lower critical solution temperature (LCST) of PNIPAm, at which microgels partially collapse. The presence of an electric charge has been attributed to the ionic initiators that are employed when FRP is performed in water and that stay anchored to microgel particles. Combining dynamic light scattering (DLS), electrophoresis, transmission electron microscopy (TEM) and atomic force microscopy (AFM) experiments, we show that collapsed ionic PNIPAm microgels undergo large mobility reversal and reentrant condensation when they are co-suspended with oppositely charged polyelectrolytes (PE) or nanoparticles (NP), while their stability remains unaffected by PE or NP addition at lower temperatures, where microgels are swollen and their charge density is low. Our results highlight a somehow double-faced electrostatic behavior of PNIPAm microgels due to their tunable charge density: they behave as quasi-neutral colloids at temperature below LCST, while they strongly interact with oppositely charged species when they are in their collapsed state. The very similar phenomenology encountered when microgels are surrounded by polylysine chains and silica nanoparticles points to the general character of this twofold behavior of PNIPAm-based colloids in water.

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24

Guo, Zongqi, Dylan Boylan, Li Shan, and Xianming Dai. "Hydrophilic reentrant SLIPS enabled flow separation for rapid water harvesting." Proceedings of the National Academy of Sciences 119, no. 36 (August 29, 2022). http://dx.doi.org/10.1073/pnas.2209662119.

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Water harvesting from air is desired for decentralized water supply wherever water is needed. When water vapor is condensed as droplets on a surface the unremoved droplets act as thermal barriers. A surface that can provide continual droplet-free areas for nucleation is favorable for condensation water harvesting. Here, we report a flow-separation condensation mode on a hydrophilic reentrant slippery liquid-infused porous surface (SLIPS) that rapidly removes droplets with diameters above 50 μm. The slippery reentrant channels lock the liquid columns inside and transport them to the end of each channel. We demonstrate that the liquid columns can harvest the droplets on top of the hydrophilic reentrant SLIPS at a high droplet removal frequency of 130 Hz/mm 2 . The sustainable flow separation without flooding increases the water harvesting rate by 110% compared to the state-of-the-art hydrophilic flat SLIPS. Such a flow-separation condensation approach paves a way for water harvesting.

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25

Liu, Liyan, Wang Fujia, Xinyi Liu, Lide Guo, Xiujun Gao, and Hongge Tan. "Self-assembly of Amphiphilic Polyelectrolytes in Trivalent Salt Solution." Physical Chemistry Chemical Physics, 2023. http://dx.doi.org/10.1039/d3cp00053b.

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Multivalent salt plays important roles in polyelectrolyte (PE) systems. Some special effects, such as ion mediated electrostatic correlation and reentrant condensation can be induced in the presence of multivalent salt....

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26

Frimpong, Asante Obed, Xiao Xu, Xu Jia, and Yuejun Zhang. "Divalent cation induced reentrant condensation behavior for lipopolysaccharides." Journal of Chemical Physics, September 16, 2022. http://dx.doi.org/10.1063/5.0111075.

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lipopolysaccharides (LPSs) are negatively charged molecules covering the surface of Gram-negative bacteria (GNB). Adding divalent cations (DCs) is important to stabilize the LPS bilayer. Here, on the basis of a coarse-grained (CG) Martini force field, we conduct molecular dynamic (MD) simulations to study the divalent cation mediated LPS interaction and the stability of the LPS membrane in a wide range of DC concentrations. By measuring the LPS binding free energy and the LPS-LPS aggregate from the association course between two LPS molecules, we find that the initial addition of DCs may significantly facilitate the aggregation of LPSs into a compact structure, while sequentially adding more DCs only unpacks the LPS aggregate and drives the dissolution of LPSs. With an increasing concentration of DCs, we find a gradual replacement of DCs to monovalent cations as condensed counterions on the LPS, which follows a sign change from negative to positive in terms of the LPS effective charge and a switch of LPSs in solution from undergoing precipitation to resolubilization on adding DCs. This interaction change in the level of two LPSs accounts for the structure variation of the LPS assembly in a larger scale, where the LPS packing rigidity in the assembly bilayer is found with a similar nonmonotonic dependence with the DC concentration. Thus, Our results demonstrate for the first time the presence of a reentrant condensation behavior for LPS molecules, which can be exploited for developing novel membrane-perturbing agents based on multivalent ions as efficient GNB antibiotics.

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27

Zhang, F., M. W. A. Skoda, R. M. J. Jacobs, S. Zorn, R. A. Martin, C. M. Martin, G. F. Clark, et al. "Reentrant Condensation of Proteins in Solution Induced by Multivalent Counterions." Physical Review Letters 101, no. 14 (September 30, 2008). http://dx.doi.org/10.1103/physrevlett.101.148101.

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28

Chien, F. T., S. G. Lin, P. Y. Lai, and C. K. Chan. "Observation of two forms of conformations in the reentrant condensation of DNA." Physical Review E 75, no. 4 (April 30, 2007). http://dx.doi.org/10.1103/physreve.75.041922.

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29

Csáthy, G., E. Kim, and M. Chan. "Condensation of 3He and Reentrant Superfluidity in Submonolayer 3He- 4He Mixture Films on H2." Physical Review Letters 88, no. 4 (January 2002). http://dx.doi.org/10.1103/physrevlett.88.045301.

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30

Krainer, Georg, Timothy J. Welsh, Jerelle A. Joseph, Jorge R. Espinosa, Sina Wittmann, Ella de Csilléry, Akshay Sridhar, et al. "Reentrant liquid condensate phase of proteins is stabilized by hydrophobic and non-ionic interactions." Nature Communications 12, no. 1 (February 17, 2021). http://dx.doi.org/10.1038/s41467-021-21181-9.

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AbstractLiquid–liquid phase separation of proteins underpins the formation of membraneless compartments in living cells. Elucidating the molecular driving forces underlying protein phase transitions is therefore a key objective for understanding biological function and malfunction. Here we show that cellular proteins, which form condensates at low salt concentrations, including FUS, TDP-43, Brd4, Sox2, and Annexin A11, can reenter a phase-separated regime at high salt concentrations. By bringing together experiments and simulations, we demonstrate that this reentrant phase transition in the high-salt regime is driven by hydrophobic and non-ionic interactions, and is mechanistically distinct from the low-salt regime, where condensates are additionally stabilized by electrostatic forces. Our work thus sheds light on the cooperation of hydrophobic and non-ionic interactions as general driving forces in the condensation process, with important implications for aberrant function, druggability, and material properties of biomolecular condensates.

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31

Zuzzi, S., C. Cametti, G. Onori, and S. Sennato. "Liposome-induced DNA compaction and reentrant condensation investigated by dielectric relaxation spectroscopy and dynamic light scattering techniques." Physical Review E 76, no. 1 (July 30, 2007). http://dx.doi.org/10.1103/physreve.76.011925.

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32

Yang, Ning, Junnosuke Okajima, and Yuka Iga. "Change in Cavitation Regime On NACA0015 Hydrofoil by Heating the Hydrofoil Surface." Journal of Fluids Engineering, February 27, 2023, 1–46. http://dx.doi.org/10.1115/1.4057004.

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Abstract An experimental study of cavitating flow on a heated NACA0015 hydrofoil was conducted in a cavitation tunnel to investigate the influence of the hydrofoil surface temperature on the cavitating flow. The cavitation behavior under different heating conditions was examined using highspeed video, and an image processing method was used to obtain the periodic characteristics of the cavitating flow. The results revealed that attached sheet cavitation and supercavitation occurred on both heated and unheated hydrofoils. However, sheet-cloud cavitation was observed only on the unheated hydrofoil, whereas transient cavitation was observed only on the heated hydrofoil. Transient cavitation also exhibited periodic growth/collapse behavior; however, there was no shedding of a large vapor cloud. Moreover, with a further increase in the hydrofoil surface temperature, transient cavitation turned into opentype cavitation. The cavitating flow exhibited a quasisteady cavity length with an open cavity closure. It was considered that the surface temperature promoted vapor generation at the cavity leading edge, which enlarged the vapor-filled fore part of the sheet cavity. This enlarged sheet cavity prevented the reentrant flow from moving upstream and thus turned the cavity closure into an open type. Once the cavity closure turned into an open type, the local disturbance led to a smaller adverse pressure gradient, which was not sufficiently strong to create a reentrant flow. In this case, if the vapor production at the cavity leading edge was sufficiently large to reach a balance with vapor condensation at the open cavity closure, the cavity would be steady.

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33

Mitra, Mithun K., and M. Muthukumar. "Theory of volume transitions in polyelectrolyte gels." MRS Proceedings 1418 (2012). http://dx.doi.org/10.1557/opl.2012.830.

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ABSTRACTWe present the key assumptions and results of a newly developed theory in order to account for the self-consistent cascade effects of counterion condensation and volume collapse of polyeletrolyte gels. In the present theory, the role of the specificity and valency of counterions on the volume transitions are also treated. These features and the fluctuations of monomer concentration and local electrolyte charge density are included on top of the familiar features of the Flory-Huggins theory and the classical rubber elasticity theory in the previously used Flory-Dusek-Patterson-Tanaka theory of polyelectrolyte gels. We have computed the swelling equilibria by satisfying the multicomponent nature of the system and the Donnan equilibria. A few major effects are illustrated in terms of the dependence of volume transition on the solvent quality, temperature, salt concentration, valency and specificity of the counterion, and polymer charge density. Criteria for the emergence of a reentrant volume transition are also derived.

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34

Xue, Yahui, Pengyu Lv, Hao Lin, and Huiling Duan. "Underwater Superhydrophobicity: Stability, Design and Regulation, and Applications." Applied Mechanics Reviews 68, no. 3 (May 1, 2016). http://dx.doi.org/10.1115/1.4033706.

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Bioinspired superhydrophobic surfaces have attracted great interest from fundamental research to engineering applications. The stability, design, and regulation of superhydrophobicity, especially in a submerged environment, have been one of the main focuses of recent efforts. This review is dedicated to illustrating the fundamental characteristics of underwater superhydrophobicity, introducing novel and effective strategies for robust design and regulation, and to providing an overview of the state-of-the-art engineering applications in drag reduction and cavitation/boiling control. First, the underlying mechanisms of wetting transition on superhydrophobic surfaces submerged underwater induced by physical phenomena including pressurization, air diffusion, fluid flow, and condensation are reviewed. The influence of the closed/open state of entrapped air cavities is differentiated. Landmark experiments demonstrating wetting transition mechanisms are surveyed. Then, novel strategies for designing robust superhydrophobic surfaces are summarized, including hierarchical, reentrant, lubricant-infused, and mechanically durable structures. Moreover, strategies for superhydrophobicity regulation are introduced, which are classified into two types: self-healing and dewetting, based on the failure regime (surface damage or meniscus collapse). The current state-of-the-art engineering applications in drag reduction and cavitation/boiling control are comprehensively reviewed. Last but not least, remaining challenges for future research are given at the conclusion.

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35

Tao, Chengjun, Zhirong Jiao, and Qiang Gu. "Reentrance of Bose-Einstein condensation in spinor atomic gases in a magnetic field." Physical Review A 79, no. 4 (April 15, 2009). http://dx.doi.org/10.1103/physreva.79.043614.

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