Shedding light on the formation of nanodroplets in aqueous by Staff Writers Washington DC (SPX) Nov 09, 2016
A team of researchers in Russia worked together to shed new light on the heterogeneous nature of a polar organic liquid mixed with water. They used laser light as a tool in two ways, dynamic light scattering and phase microscopy, that allowed them to demonstrate the existence of stable nanodroplets of tetrahydrofuran (THF) in the bulk of aqueous electrolyte solutions and to develop a new theory that explains the spontaneous generation of heterogeneous nanoparticles in aqueous solutions of polar organic solutes in terms of nanodroplet formation due to "twinkling" hydrogen bonds. Until recently it was thought that heterogeneous particles in binary mixtures of polar organic compounds could either be gas nanobubbles or giant stable molecular complexes, formed by the molecules of the solute or solvent. In an article appearing this week in the Journal of Chemical Physics, from AIP Publishing, a research team that included scientists from four different Moscow institutions used THF, which has infinite solubility in water and which, in aqueous solutions of low THF concentrations, allows observation of abnormally high scattering of light due to the spontaneous formation of some heterogeneous centers. Combining dynamic light scattering with a novel experimental technique called laser phase microscopy that can measure the refractive index of nanometer-scale objects in liquids in addition to their sizes, allowed them to determine that the nanodroplets being observed in aqueous mixtures of THF at low concentrations basically consist of pure THF. "We began by repeating previous laser light scattering experiments using dynamic light scattering, which actually confirmed the abnormally high level of scattering in this concentration range; demonstrating that the scattering centers are nanometer-scale particles," said N.F. Bunkin, a professor from Bauman Moscow State Technical University. Since the two pure liquids are mixed in a fixed ratio, these particles should consist of THF and water in a certain ratio. The problem, however, is that the light scattering experiments cannot be used to determine the percentage of these components in the scattering particles. "We managed to solve this problem by using a unique phase microscope that we developed in collaboration with other scientists from Russia; one that can measure not only the size of the nanoparticles in a liquid, but also determine their refractive index," Bunkin explained. "We found that the refractive index of the scattering objects in THF-water mixtures practically coincides with the refractive index of pure THF though, in accordance with the reference data, such THF nanodroplets just cannot exist in the solution of such concentration." However, for the research team the biggest challenge was not the experiment, or even the development of the new microscope, but the development of a theory that incorporated and explained their results. Intuition suggests that the spontaneous formation of pure THF droplets in dilute aqueous solutions should be somehow controlled by the parameters of the interaction of water and THF molecules via hydrogen bonding. Roughly speaking, the THF molecule can either form a hydrogen bond with a neighboring water molecule, or not. If quite a large amount of THF molecules, localized in a nanometer-scaled area of the liquid solution, simultaneously rupture the hydrogen bonds with the neighboring water molecules, a nanodroplet of pure THF is created in this area, a fact was observed in this experiment. The team is already looking ahead to the next steps in this research. The kinetics of nanodroplet nucleation is still beyond the scope of their proposed model. They are planning to carry out similar experiments with aqueous solutions of organic liquids from the furan group which has different polarizability and dipole moments, and with solutions of water isotopes (H20, D20 and deuterium depleted water) that have different energies of intermolecular hydrogen bond and to explore the role of dissolved gas. The article, "Droplet-like heterogeneity of aqueous tetrahydrofuran solutions at the submicrometer scale," is authored by N.F. Bunkin, A.V. Shkirin, G.A. Lyakhov, A.V. Kobelev, N.V. Penkov, S.V. Ugraitskaya and E.E. Fesenko Jr. The article appeared in the Journal of Chemical Physics November 8, 2016 [DOI: 10.1063/1.4966187]
Related Links American Institute of Physics Nano Technology News From SpaceMart.com Computer Chip Architecture, Technology and Manufacture
|
|
The content herein, unless otherwise known to be public domain, are Copyright 1995-2024 - Space Media Network. All websites are published in Australia and are solely subject to Australian law and governed by Fair Use principals for news reporting and research purposes. AFP, UPI and IANS news wire stories are copyright Agence France-Presse, United Press International and Indo-Asia News Service. ESA news reports are copyright European Space Agency. All NASA sourced material is public domain. Additional copyrights may apply in whole or part to other bona fide parties. All articles labeled "by Staff Writers" include reports supplied to Space Media Network by industry news wires, PR agencies, corporate press officers and the like. Such articles are individually curated and edited by Space Media Network staff on the basis of the report's information value to our industry and professional readership. Advertising does not imply endorsement, agreement or approval of any opinions, statements or information provided by Space Media Network on any Web page published or hosted by Space Media Network. General Data Protection Regulation (GDPR) Statement Our advertisers use various cookies and the like to deliver the best ad banner available at one time. All network advertising suppliers have GDPR policies (Legitimate Interest) that conform with EU regulations for data collection. By using our websites you consent to cookie based advertising. If you do not agree with this then you must stop using the websites from May 25, 2018. Privacy Statement. Additional information can be found here at About Us. |