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Journal articles on the topic 'Hydrophobic ion'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Aryal, Prafulla, Mark S. P. Sansom, and Stephen J. Tucker. "Hydrophobic Gating in Ion Channels." Journal of Molecular Biology 427, no. 1 (January 2015): 121–30. http://dx.doi.org/10.1016/j.jmb.2014.07.030.

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2

Loginova, Dar’ya V., Alexander S. Lileev, Andrey K. Lyashchenko, and Valery S. Kharkin. "Hydrophobic hydration of the propionate ion." Mendeleev Communications 13, no. 2 (January 2003): 68–70. http://dx.doi.org/10.1070/mc2003v013n02abeh001684.

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3

López-León, Teresa, Juan Luis Ortega-Vinuesa, and Delfina Bastos-González. "Ion-Specific Aggregation of Hydrophobic Particles." ChemPhysChem 13, no. 9 (May 3, 2012): 2382–91. http://dx.doi.org/10.1002/cphc.201200120.

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4

Cui, Xin, Jing Liu, Lei Xie, Jun Huang, and Hongbo Zeng. "Interfacial ion specificity modulates hydrophobic interaction." Journal of Colloid and Interface Science 578 (October 2020): 135–45. http://dx.doi.org/10.1016/j.jcis.2020.05.091.

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5

Chui, Jonathan K. W., and T. M. Fyles. "Cyclodextrin ion channels." Org. Biomol. Chem. 12, no. 22 (2014): 3622–34. http://dx.doi.org/10.1039/c4ob00480a.

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6

Ristroph, Kurt D., and Robert K. Prud'homme. "Hydrophobic ion pairing: encapsulating small molecules, peptides, and proteins into nanocarriers." Nanoscale Advances 1, no. 11 (2019): 4207–37. http://dx.doi.org/10.1039/c9na00308h.

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Hydrophobic ion pairing has emerged as a method to modulate the solubility of charged hydrophilic molecules ranging in class from small molecules to large enzymes. Here we review the application of hydrophobic ion pairing for encapsulating charged hydrophilic molecules into nanocarriers.

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7

Song, Chen, and Ben Corry. "Intrinsic Ion Selectivity of Narrow Hydrophobic Pores." Journal of Physical Chemistry B 113, no. 21 (May 28, 2009): 7642–49. http://dx.doi.org/10.1021/jp810102u.

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8

Maha, Abu Hajleh, and Al-Dujaili Emad A.S. "HYDROPHOBIC ION-PAIRED DRUG DELIVERY SYSTEM: A REVIEW." INDIAN DRUGS 57, no. 01 (January 28, 2020): 7–18. http://dx.doi.org/10.53879/id.57.01.12071.

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Hydrophobic ion-pairing (HIP) complexation technique has been displayed to modify the physicochemical properties, solubility, oral absorption, bioavailability, and the lipophilicity of an ionic drug in the lipid phase. This could affect a higher permeation through biological membranes. HIP complexation was considered through the formation of a neutral molecule by electrostatic interaction of ionizable groups of drugs with oppositely charged functional groups of a complex-forming agent. Subsequently, this ion-pair may encapsulate into many delivery systems. The objective of this manuscript was to study the effectiveness of ion-pair complextion and cover the update application of this strategy through several routes of administration such as ocular, oral, pulmonary, transdermal, and parenteral.

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9

Liu, Yanni, Zhi Wang, Mengqi Shi, Nan Li, Song Zhao, and Jixiao Wang. "Carbonic anhydrase inspired poly(N-vinylimidazole)/zeolite Zn-β hybrid membranes for CO2 capture." Chemical Communications 54, no. 52 (2018): 7239–42. http://dx.doi.org/10.1039/c8cc03656j.

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10

Inoue, Youichi, Yasuhiro Yoshimura, Yukiko Ikeda, and Akiomi Kohno. "Ultra-hydrophobic fluorine polymer by Ar-ion bombardment." Colloids and Surfaces B: Biointerfaces 19, no. 3 (December 2000): 257–61. http://dx.doi.org/10.1016/s0927-7765(00)00163-6.

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11

North, R. Alan. "Families of ion channels with two hydrophobic segments." Current Opinion in Cell Biology 8, no. 4 (August 1996): 474–83. http://dx.doi.org/10.1016/s0955-0674(96)80023-8.

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12

Dill, Ken A., Thomas M. Truskett, Vojko Vlachy, and Barbara Hribar-Lee. "Modeling Water, the Hydrophobic Effect, and Ion Solvation." Annual Review of Biophysics and Biomolecular Structure 34, no. 1 (June 2005): 173–99. http://dx.doi.org/10.1146/annurev.biophys.34.040204.144517.

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13

Rao, Shanlin, Gianni Klesse, Stephen J. Tucker, and Mark S. P. Sansom. "Hydrophobic Gating: Examination of Recent Ion Channel Structures." Biophysical Journal 114, no. 3 (February 2018): 134a. http://dx.doi.org/10.1016/j.bpj.2017.11.762.

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14

Feng, Lixin, Alexandra De Dille, Vicky J. Jameson, Leia Smith, William S. Dernell, and Mark C. Manning. "Improved potency of cisplatin by hydrophobic ion pairing." Cancer Chemotherapy and Pharmacology 54, no. 5 (July 29, 2004): 441–48. http://dx.doi.org/10.1007/s00280-004-0840-z.

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15

Huang, Zhi De. "Influence Experimental Study on HPI Hydrophobic Compound Hole Plug Concrete Performance." Applied Mechanics and Materials 584-586 (July 2014): 1527–30. http://dx.doi.org/10.4028/www.scientific.net/amm.584-586.1527.

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Forming three groups concrete of different gelled material systems, the effecting of HPI hydrophobic compound hole plug on concrete compressive strength, chloride ion permeability resistance and water absorption performance were studied taking CALTITE and 3CC for example. Studies have shown that this kind of polymer can reduce compressive strength, but can improve chloride ion permeability resistance and hydrophobic property of concrete.

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16

Li, Hui, Joseph S. Francisco, and Xiao Cheng Zeng. "Unraveling the mechanism of selective ion transport in hydrophobic subnanometer channels." Proceedings of the National Academy of Sciences 112, no. 35 (August 17, 2015): 10851–56. http://dx.doi.org/10.1073/pnas.1513718112.

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Recently reported synthetic organic nanopore (SONP) can mimic a key feature of natural ion channels, i.e., selective ion transport. However, the physical mechanism underlying the K+/Na+ selectivity for the SONPs is dramatically different from that of natural ion channels. To achieve a better understanding of the selective ion transport in hydrophobic subnanometer channels in general and SONPs in particular, we perform a series of ab initio molecular dynamics simulations to investigate the diffusivity of aqua Na+ and K+ ions in two prototype hydrophobic nanochannels: (i) an SONP with radius of 3.2 Å, and (ii) single-walled carbon nanotubes (CNTs) with radii of 3–5 Å (these radii are comparable to those of the biological potassium K+ channels). We find that the hydration shell of aqua Na+ ion is smaller than that of aqua K+ ion but notably more structured and less yielding. The aqua ions do not lower the diffusivity of water molecules in CNTs, but in SONP the diffusivity of aqua ions (Na+ in particular) is strongly suppressed due to the rugged inner surface. Moreover, the aqua Na+ ion requires higher formation energy than aqua K+ ion in the hydrophobic nanochannels. As such, we find that the ion (K+ vs. Na+) selectivity of the (8, 8) CNT is ∼20× higher than that of SONP. Hence, the (8, 8) CNT is likely the most efficient artificial K+ channel due in part to its special interior environment in which Na+ can be fully solvated, whereas K+ cannot. This work provides deeper insights into the physical chemistry behind selective ion transport in nanochannels.

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17

Pandit, Bijan, Abhijit Sarkar, and Biswajit Sinha. "Solution thermodynamics of sodium pyruvate in aqueous glycine solutions at T 298.15-313.15 K." Journal of the Serbian Chemical Society 81, no. 11 (2016): 1283–94. http://dx.doi.org/10.2298/jsc151031034p.

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In this study we investigated the effects of sodium pyruvate on the solution thermodynamics of glycine in terms of the solute-solute and solute-solvent interactions in aqueous solutions. Measured density and viscosity were used to derive apparent molar volumes (?V), standard partial molar volumes (?V0) and viscosity B-coefficients at 298.15, 303.15 K, 308.15, and 318.15 K under ambient pressure. The interactions are further discussed in terms of ion-dipolar, hydrophobic- hydrophobic, hydrophilic-hydrophobic group interactions. The activation parameters of viscous flow were also discussed in terms of transition state theory. The overall results indicated that ion-hydrophilic and hydrophilic-hydrophilic group interactions are predominant in the ternary solutions.

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18

Sagehashi, M., T. Fukuda, T. Fujii, Y. Sakai, and A. Sakoda. "Elution and adsorptive concentration of Japanese cedar (Cryptomeria japonica) pollen allergen in environmental water." Water Science and Technology 52, no. 8 (October 1, 2005): 37–43. http://dx.doi.org/10.2166/wst.2005.0219.

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Elution of Japanese cedar pollen allergens (Cry j I and others) from pollen grains and its adsorptive concentration onto hydrophobic and hydrophilic surfaces were investigated using the surface plasmon resonance technique. Results showed that the allergen elution was obviously enhanced when the ion concentration was higher than that within the human body, indicating that the pollen tend to release its allergen in environmental water having a high ion concentration. However, higher adsorption capacity was observed on hydrophobic surface than hydrophilic surface. These results indicate that water puddles on roadsides beside heavy traffic including large amounts of ion compounds and hydrophobic diesel exhaust particles (DEPs) are a pollen allergen-DEP complex generator. DEPs are easily absorbed into the living body; therefore these mechanisms may be responsible for causing the highest incidence of pollinosis among residents living alongside roads with heavy automobile traffic.

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19

Trick, Jemma L., Prafulla Aryal, Stephen J. Tucker, and Mark S. P. Sansom. "Molecular simulation studies of hydrophobic gating in nanopores and ion channels." Biochemical Society Transactions 43, no. 2 (April 1, 2015): 146–50. http://dx.doi.org/10.1042/bst20140256.

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Gating in channels and nanopores plays a key role in regulating flow of ions across membranes. Molecular simulations provide a ‘computational microscope’ which enables us to examine the physical nature of gating mechanisms at the level of the single channel molecule. Water enclosed within the confines of a nanoscale pore may exhibit unexpected behaviour. In particular, if the molecular surfaces lining the pore are hydrophobic this promotes de-wetting of the pore. De-wetting is observed as stochastic liquid–vapour transitions within a pore, and may lead to functional closure of a pore to the flow of ions and/or water. Such behaviour was first observed in simulations of simple model nanopores and referred to as ‘hydrophobic gating’. Simulations of both the nicotinic acetylcholine receptor and of TWIK-1 potassium channels (the latter alongside experimental studies) suggest hydrophobic gating may occur in some biological ion channels. Current studies are focused on designing hydrophobic gates into biomimetic nanopores.

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20

Langan, Patricia S., Venu Gopal Vandavasi, Wojciech Kopec, Brendan Sullivan, Pavel V. Afonne, Kevin L. Weiss, Bert L. de Groot, and Leighton Coates. "The structure of a potassium-selective ion channel reveals a hydrophobic gate regulating ion permeation." IUCrJ 7, no. 5 (July 25, 2020): 835–43. http://dx.doi.org/10.1107/s2052252520008271.

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Protein dynamics are essential to function. One example of this is the various gating mechanisms within ion channels, which are transmembrane proteins that act as gateways into the cell. Typical ion channels switch between an open and closed state via a conformational transition which is often triggered by an external stimulus, such as ligand binding or pH and voltage differences. The atomic resolution structure of a potassium-selective ion channel named NaK2K has allowed us to observe that a hydrophobic residue at the bottom of the selectivity filter, Phe92, appears in dual conformations. One of the two conformations of Phe92 restricts the diameter of the exit pore around the selectivity filter, limiting ion flow through the channel, while the other conformation of Phe92 provides a larger-diameter exit pore from the selectivity filter. Thus, it can be concluded that Phe92 acts as a hydrophobic gate, regulating the flow of ions through the selectivity filter.

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21

Liu, Zizhao, S. Ranil Wickramasinghe, and Xianghong Qian. "Ion-specificity in protein binding and recovery for the responsive hydrophobic poly(vinylcaprolactam) ligand." RSC Advances 7, no. 58 (2017): 36351–60. http://dx.doi.org/10.1039/c7ra06022j.

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The conformational switch between the hydrophobic state and hydrophilic state of thermo-responsive poly(vinylcaprolactam) (PVCL) has great potential for protein purification as a hydrophobic interaction chromatography ligand.

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22

Fransson, Bengt. "Reversed-phase ion-pair chromatography of basic, hydrophobic peptides." Journal of Chromatography A 361 (January 1986): 161–67. http://dx.doi.org/10.1016/s0021-9673(01)86903-x.

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23

Neale, Chris, Nilmadhab Chakrabarti, Pawel Pomorski, Emil F. Pai, and Régis Pomès. "Hydrophobic Gating of Ion Permeation in Magnesium Channel CorA." PLOS Computational Biology 11, no. 7 (July 16, 2015): e1004303. http://dx.doi.org/10.1371/journal.pcbi.1004303.

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24

Chow, Brian J., Weiyi Lu, Aijie Han, Hyuck Lim, and Yu Qiao. "Ion repelling effect of nanopores in a hydrophobic zeolite." Journal of Materials Research 26, no. 9 (April 26, 2011): 1164–67. http://dx.doi.org/10.1557/jmr.2011.73.

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25

Gao, Ang, Richard C. Remsing, and John D. Weeks. "Short solvent model for ion correlations and hydrophobic association." Proceedings of the National Academy of Sciences 117, no. 3 (January 7, 2020): 1293–302. http://dx.doi.org/10.1073/pnas.1918981117.

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Coulomb interactions play a major role in determining the thermodynamics, structure, and dynamics of condensed-phase systems, but often present significant challenges. Computer simulations usually use periodic boundary conditions to minimize corrections from finite cell boundaries but the long range of the Coulomb interactions generates significant contributions from distant periodic images of the simulation cell, usually calculated by Ewald sum techniques. This can add significant overhead to computer simulations and hampers the development of intuitive local pictures and simple analytic theory. In this paper, we present a general framework based on local molecular field theory to accurately determine the contributions from long-ranged Coulomb interactions to the potential of mean force between ionic or apolar hydrophobic solutes in dilute aqueous solutions described by standard classical point charge water models. The simplest approximation leads to a short solvent (SS) model, with truncated solvent–solvent and solute–solvent Coulomb interactions and long-ranged but screened Coulomb interactions only between charged solutes. The SS model accurately describes the interplay between strong short-ranged solute core interactions, local hydrogen-bond configurations, and long-ranged dielectric screening of distant charges, competing effects that are difficult to capture in standard implicit solvent models.

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26

Zhou, Huiyu, Corinne Lengsfeld, David J. Claffey, James A. Ruth, Brooks Hybertson, Theodore W. Randolph, Ka‐Yun Ng, and Mark C. Manning. "Hydrophobic Ion Pairing of Isoniazid Using a Prodrug Approach." Journal of Pharmaceutical Sciences 91, no. 6 (June 2002): 1502–11. http://dx.doi.org/10.1002/jps.10116.

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27

Song, Lian, Xiong‐Fei Zhang, Zhongguo Wang, Yunhua Bai, Yi Feng, and Jianfeng Yao. "Metal‐Ion Induced Surface Modification for Durable Hydrophobic Wood." Advanced Materials Interfaces 7, no. 22 (October 5, 2020): 2001166. http://dx.doi.org/10.1002/admi.202001166.

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28

Bunton, Clifford A., and Ellen L. Dorwin. "Reactions of carbocations with a functionalized hydrophobic ammonium ion." Journal of Organic Chemistry 51, no. 22 (October 1986): 4093–96. http://dx.doi.org/10.1021/jo00372a001.

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29

Rao, Shanlin, Charlotte I. Lynch, Gianni Klesse, Georgia E. Oakley, Phillip J. Stansfeld, Stephen J. Tucker, and Mark S. P. Sansom. "Water and hydrophobic gates in ion channels and nanopores." Faraday Discussions 209 (2018): 231–47. http://dx.doi.org/10.1039/c8fd00013a.

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30

López-León, Teresa, José Manuel López-López, Gerardo Odriozola, Delfi Bastos-González, and Juan Luis Ortega-Vinuesa. "Ion-induced reversibility in the aggregation of hydrophobic colloids." Soft Matter 6, no. 6 (2010): 1114. http://dx.doi.org/10.1039/b922621d.

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31

Texter, John, Paul Ziemer, Steve Rhoades, and Daniel Clemans. "Bactericidal silver ion delivery into hydrophobic coatings with surfactants." Journal of Industrial Microbiology & Biotechnology 34, no. 8 (June 19, 2007): 571–75. http://dx.doi.org/10.1007/s10295-007-0228-2.

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32

Song, Chen, and Ben Corry. "Hydrophobic Selectivity And Electrostatic Gating In Narrow Ion Channels." Biophysical Journal 96, no. 3 (February 2009): 661a. http://dx.doi.org/10.1016/j.bpj.2008.12.3492.

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33

Ding, Xin‐Lei, Zeng‐Qiang Wu, Zhong‐Qiu Li, and Xing‐Hua Xia. "Electric Field Driven Surface Ion Transport in Hydrophobic Nanopores †." Chinese Journal of Chemistry 39, no. 6 (May 9, 2021): 1511–16. http://dx.doi.org/10.1002/cjoc.202000730.

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34

Lynch, Charlotte I., Shanlin Rao, Gianni Klesse, Stephen J. Tucker, and Mark S. P. Sansom. "Modelling Water Behaviour in Hydrophobic Gates of Ion Channels." Biophysical Journal 120, no. 3 (February 2021): 157a. http://dx.doi.org/10.1016/j.bpj.2020.11.1133.

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35

Tsujimoto, Kazuo, Akio Hayashia, Tae Joung Ha, and Isao Kubo. "Anacardic Acids and Ferric Ion Chelation." Zeitschrift für Naturforschung C 62, no. 9-10 (October 1, 2007): 710–16. http://dx.doi.org/10.1515/znc-2007-9-1014.

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6-Pentadeca(e)nylsalicylic acids isolated from the cashew Anacardium occidentale L. (Anacardiaceae), commonly known as anacardic acids, inhibited the linoleic acid peroxidation catalyzed by soybean lipoxygenase-1 (EC 1.13.11.12, type 1) competitively without prooxidant effects. Their parent compound, salicylic acid, did not have this inhibitory activity up to 800 μm, indicating that the pentadeca(e)nyl group is an essential element to elicit the activity. The inhibition is attributed to its ability to chelate iron in the enzyme. Thus, anacardic acids chelate iron in the active site of the enzyme and then the hydrophobic tail portion slowly begins to interact with the hydrophobic domain close to the active site. Formation of the anacardic acids-ferric ion complex was detected in the ratio of 2:1 as the base peak in the negative ion electrospray ionization mass spectrometry. Hence, anacardic acids inhibit both Eox and Ered forms.

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36

Sarkar, Abhijit, and Biswajit Sinha. "Solution thermodynamics of aqueous nicotinic acid solutions in presence of tetrabutylammonium hydrogen sulphate." Journal of the Serbian Chemical Society 78, no. 8 (2013): 1225–40. http://dx.doi.org/10.2298/jsc111212027s.

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In this study we investigated the effects of tetrabutylammonium hydrogen sulphate (Bu4NHSO4) on the solute-solute and solute-solvent interactions in the aqueous solutions of nicotinic acid in terms of apparent molar volumes (?V), standard partial molar volumes (?V0) and viscosity B-coefficients at 298.15, 308.15, and 318.15 K under ambient pressure. These interactions are further discussed in terms of ion-dipolar, hydrophobic- hydrophobic, hydrophilic-hydrophobic group interactions. The activation parameters of viscous flow for Bu4NHSO4 in the aqueous solutions of nicotinic acid were discussed in terms of transition state theory. The overall results indicated that ion-hydrophilic and hydrophilic-hydrophilic group interactions are predominant in the aqueous solutions of nicotinic acid and Bu4NHSO4 has a dehydration effect on the hydrated nicotinic acid.

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37

Naranjo, David, Hans Moldenhauer, Matías Pincuntureo, and Ignacio Díaz-Franulic. "Pore size matters for potassium channel conductance." Journal of General Physiology 148, no. 4 (September 12, 2016): 277–91. http://dx.doi.org/10.1085/jgp.201611625.

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Ion channels are membrane proteins that mediate efficient ion transport across the hydrophobic core of cell membranes, an unlikely process in their absence. K+ channels discriminate K+ over cations with similar radii with extraordinary selectivity and display a wide diversity of ion transport rates, covering differences of two orders of magnitude in unitary conductance. The pore domains of large- and small-conductance K+ channels share a general architectural design comprising a conserved narrow selectivity filter, which forms intimate interactions with permeant ions, flanked by two wider vestibules toward the internal and external openings. In large-conductance K+ channels, the inner vestibule is wide, whereas in small-conductance channels it is narrow. Here we raise the idea that the physical dimensions of the hydrophobic internal vestibule limit ion transport in K+ channels, accounting for their diversity in unitary conductance.

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38

SASAKURA, Keisuke, Shintaro KUBOTA, Jun ONISHI, Shunsuke OZAKI, Kenji KANO, and Osamu SHIRAI. "Ion Transport across a Bilayer Lipid Membrane in the Presence of a Hydrophobic Ion." Electrochemistry 76, no. 8 (2008): 597–99. http://dx.doi.org/10.5796/electrochemistry.76.597.

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39

Wang, Lizhu, and Michael A. Hickner. "Highly ordered ion-conducting block copolymers by hydrophobic block modification." Journal of Materials Chemistry A 4, no. 40 (2016): 15437–49. http://dx.doi.org/10.1039/c6ta05308d.

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Block copolymer-based AEMs provide advanced materials with tunable properties through manipulation of both the ionic domains for high conductivity and the hydrophobic domains for mechanical integrity.

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40

Hwang, Junho, Tatsuki Sekimoto, Wei-Lun Hsu, Sho Kataoka, Akira Endo, and Hirofumi Daiguji. "Thermal dependence of nanofluidic energy conversion by reverse electrodialysis." Nanoscale 9, no. 33 (2017): 12068–76. http://dx.doi.org/10.1039/c7nr04387b.

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41

Rao, Shanlin, Gianni Klesse, Phillip J. Stansfeld, Stephen J. Tucker, and Mark S. P. Sansom. "A heuristic derived from analysis of the ion channel structural proteome permits the rapid identification of hydrophobic gates." Proceedings of the National Academy of Sciences 116, no. 28 (June 24, 2019): 13989–95. http://dx.doi.org/10.1073/pnas.1902702116.

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Ion channel proteins control ionic flux across biological membranes through conformational changes in their transmembrane pores. An exponentially increasing number of channel structures captured in different conformational states are now being determined; however, these newly resolved structures are commonly classified as either open or closed based solely on the physical dimensions of their pore, and it is now known that more accurate annotation of their conductive state requires additional assessment of the effect of pore hydrophobicity. A narrow hydrophobic gate region may disfavor liquid-phase water, leading to local dewetting, which will form an energetic barrier to water and ion permeation without steric occlusion of the pore. Here we quantify the combined influence of radius and hydrophobicity on pore dewetting by applying molecular dynamics simulations and machine learning to nearly 200 ion channel structures. This allows us to propose a simple simulation-free heuristic model that rapidly and accurately predicts the presence of hydrophobic gates. This not only enables the functional annotation of new channel structures as soon as they are determined, but also may facilitate the design of novel nanopores controlled by hydrophobic gates.

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42

Kozuch, Daniel J., Kurt Ristroph, Robert K. Prud’homme, and Pablo G. Debenedetti. "Insights into Hydrophobic Ion Pairing from Molecular Simulation and Experiment." ACS Nano 14, no. 5 (April 30, 2020): 6097–106. http://dx.doi.org/10.1021/acsnano.0c01835.

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43

Schamberger, Jens, and Ronald J. Clarke. "Hydrophobic Ion Hydration and the Magnitude of the Dipole Potential." Biophysical Journal 82, no. 6 (June 2002): 3081–88. http://dx.doi.org/10.1016/s0006-3495(02)75649-x.

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44

Liu, Zhiliang, Xinghua Chang, Teng Wang, Wei Li, Haidong Ju, Xinyao Zheng, Xiuqi Wu, Cong Wang, Jie Zheng, and Xingguo Li. "Silica-Derived Hydrophobic Colloidal Nano-Si for Lithium-Ion Batteries." ACS Nano 11, no. 6 (June 7, 2017): 6065–73. http://dx.doi.org/10.1021/acsnano.7b02021.

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45

Naik, Ashok Kumar, Supriya Priyambada Biswal, Prabhudatta Hota, Mitali Mithilesh, Manav Saxena, and Pramila K. Misra. "Ion-Adduct with Hydrophobic Scaffold: Synthesis, Characterization and Solution Behaviour." Materials Today: Proceedings 9 (2019): 568–77. http://dx.doi.org/10.1016/j.matpr.2018.10.377.

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46

Ohwaki, Takeshi, and Yasunori Taga. "Changes in hydrophobic properties of glass surfaces by ion implantation." Journal of Vacuum Science & Technology A: Vacuum, Surfaces, and Films 8, no. 3 (May 1990): 2173–76. http://dx.doi.org/10.1116/1.577036.

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47

Shvedene, N. V., D. V. Chernyshev, Yu P. Gromova, M. Yu Nemilova, and I. V. Pletnev. "Hydrophobic ionic liquids in plasticized membranes of ion-selective eletctrodes." Journal of Analytical Chemistry 65, no. 8 (August 2010): 861–65. http://dx.doi.org/10.1134/s1061934810080174.

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48

Zhang, Shuang, Lanwei Zhang, Yuehua Jiao, Hongbo Li, Nditange Shigwedha, Yingchun Zhang, Huaxi Yi, and Xue Han. "Lactobacillus delbrueckiisubsp.bulgaricusProteinase: Purification by Ion-Exchange and Hydrophobic Interaction Chromatography." International Journal of Food Properties 18, no. 7 (October 15, 2014): 1560–67. http://dx.doi.org/10.1080/10942912.2014.921199.

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49

Zukuls, A., and G. Mezinskis. "Hydrophobic properties of high Fe3+ ion containing Fe2O3-TiO2 coatings." IOP Conference Series: Materials Science and Engineering 251 (October 2017): 012109. http://dx.doi.org/10.1088/1757-899x/251/1/012109.

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Korfhagen, Joseph, Ana C. Dias-Cabral, and Marvin E. Thrash. "Nonspecific Effects of Ion Exchange and Hydrophobic Interaction Adsorption Processes." Separation Science and Technology 45, no. 14 (September 15, 2010): 2039–50. http://dx.doi.org/10.1080/01496391003793876.

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