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Journal articles on the topic 'Air – water interfaces'

Author: Grafiati
Published: 4 June 2021
Last updated: 2 February 2022

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1

Fendler, Janos H. "Nanoparticles at air/water interfaces." Current Opinion in Colloid & Interface Science 1, no. 2 (April 1996): 202–7. http://dx.doi.org/10.1016/s1359-0294(96)80005-7.

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2

Zhao, Yani, and Marek Cieplak. "Proteins at air–water and oil–water interfaces in an all-atom model." Physical Chemistry Chemical Physics 19, no. 36 (2017): 25197–206. http://dx.doi.org/10.1039/c7cp03829a.

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Proteins with different hydrophobicities are studied at the air–water and oil–water interfaces. The all-atom simulating results are consistent with the coarse-grained interfacial model. Proteins are found to be coupled stronger but diffused slower at the oil–water interface than the air–water one.
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3

Nikiforidis, Constantinos V., Christos Ampatzidis, Sofia Lalou, Elke Scholten, Thodoris D. Karapantsios, and Vassilios Kiosseoglou. "Purified oleosins at air–water interfaces." Soft Matter 9, no. 4 (2013): 1354–63. http://dx.doi.org/10.1039/c2sm27118d.

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4

Johannsen, E. C., J. B. Chung, C. H. Chang, and E. I. Franses. "Lipid transport to air/water interfaces." Colloids and Surfaces 53, no. 1 (January 1991): 117–34. http://dx.doi.org/10.1016/0166-6622(91)80039-q.

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5

Eastoe, Julian, Adrian Downer, Alison Paul, David C. Steytler, Emily Rumsey, Jeff Penfold, and Richard K. Heenan. "Fluoro-surfactants at air/water and water/CO2 interfaces." Physical Chemistry Chemical Physics 2, no. 22 (2000): 5235–42. http://dx.doi.org/10.1039/b005858k.

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6

Poirier, Alexandre, Antonio Stocco, Romain Kapel, Martin In, Laurence Ramos, and Amélie Banc. "Sunflower Proteins at Air–Water and Oil–Water Interfaces." Langmuir 37, no. 8 (February 18, 2021): 2714–27. http://dx.doi.org/10.1021/acs.langmuir.0c03441.

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7

Kahlweit, M., G. Busse, and J. Jen. "Adsorption of amphiphiles at water/air interfaces." Journal of Physical Chemistry 95, no. 14 (July 1991): 5580–86. http://dx.doi.org/10.1021/j100167a040.

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8

Zhao, Yumeng, Boyoung Jeong, Dong-Hun Kang, and Sheng Dai. "Impacts of motile Escherichia coli on air-water surface tension." E3S Web of Conferences 205 (2020): 08003. http://dx.doi.org/10.1051/e3sconf/202020508003.

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Immiscible multiphase flow in porous media is largely affected by interfacial properties, manifested in contact angle and surface tension. The gas-liquid surface tension can be significantly altered by suspended particles at the interface. Particle-laden interfaces have unique properties, for example, a lower surface tension of interfaces laden with surfactants or nanoparticles. This study investigates the impacts of a motile bacterium Escherichia coli (E. coli, strain ATCC 9637) on the air-water surface tension. Methods of the maximum bubble pressure, the du Noüy ring, and the pendant droplet are used to measure the surface tension of the motile-bacteria-laden interfaces. Measured surface tension remains independent to the E. coli concentration when using the maximum bubble pressure method, decreases with increased E. coli concentration in the du Noüy ring method, and presents time-dependent changes by the pendant drop method. The analyses show that the discrepancies may come from the different convection-diffusion processes of E. coli in the flow among various testing methods.
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9

Caminati, G., and G. Gabrielli. "Polystyrene sulfonate adsorption at water—graphon and water—air interfaces." Colloids and Surfaces A: Physicochemical and Engineering Aspects 70, no. 1 (January 1993): 1–14. http://dx.doi.org/10.1016/0927-7757(93)80491-v.

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10

Nayak, Alpana, and K. A. Suresh. "Discogen−DNA Complex Films at Air−Water and Air−Solid Interfaces." Journal of Physical Chemistry B 112, no. 10 (March 2008): 2930–36. http://dx.doi.org/10.1021/jp710084q.

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11

Godin, Oleg A. "Anomalous transmission of infrasound through air-water and air-ground interfaces." Journal of the Acoustical Society of America 132, no. 3 (September 2012): 2047. http://dx.doi.org/10.1121/1.4755528.

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12

Kumar, Bharat, A. K. Prajapati, M. C. Varia, and K. A. Suresh. "Novel Mesogenic Azobenzene Dimer at Air−Water and Air−Solid Interfaces." Langmuir 25, no. 2 (January 20, 2009): 839–44. http://dx.doi.org/10.1021/la8030733.

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13

Polavarapu, Prasad L., and Zhengyu Deng. "Differential Polarized Reflectance Spectroscopy at Air/Water and Air/Metal Interfaces." Applied Spectroscopy 50, no. 1 (January 1996): 91–97. http://dx.doi.org/10.1366/0003702963906807.

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We report the direct measurement of differential polarized reflectance spectra for samples at air/water and air/metal interfaces. The central component for these measurements is a polarization-division interferometer (PDI). This interferometer uses an in-house-designed beamsplitter constructed in-house from a BaF2 polarizer and a matching substrate. In conjunction with a linear polarizer in front of the source and two rooftop mirrors, one in each arm of the interferometer, the PDI divides the input beam into two orthogonal linear polarization components, recombines them for interference at the beamsplitter, and directs the output beam at 90° to the direction of the input beam. Collimated light rays exiting the interferometer are focused by an f/5 lens and bent from the horizontal propagating axis by a ZnSe wedge to give an angle of incidence of ∼75°, at the sample. The reflected rays are brought back to the horizontal propagation direction by another ZnSe wedge and focused onto the detector by an f/1 lens. The interferogram obtained in this manner represents the differential polarized reflectance interferogram whose cosine Fourier transform directly gives the differential polarized reflectance spectrum. Thus, these spectra were obtained without need for the commonly used photoelastic modulator. Representative spectra for monolayers on a water surface and for samples on a gold surface are presented.
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14

Graciaa, A., P. Creux, J. Lachaise, and R. S. Schechter. "Competitive adsorption of surfactants at air/water interfaces." Journal of Colloid and Interface Science 261, no. 2 (May 2003): 233–37. http://dx.doi.org/10.1016/s0021-9797(03)00052-3.

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15

BANNER, MICHAEL L., and WILLIAM L. PEIRSON. "Tangential stress beneath wind-driven air–water interfaces." Journal of Fluid Mechanics 364 (June 10, 1998): 115–45. http://dx.doi.org/10.1017/s0022112098001128.

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The detailed structure of the aqueous surface sublayer flow immediately adjacent to the wind-driven air–water interface is investigated in a laboratory wind-wave flume using particle image velocimetry (PIV) techniques. The goal is to investigate quantitatively the character of the flow in this crucial, very thin region which is often disrupted by microscale breaking events. In this study, we also examine critically the conclusions of Okuda, Kawai & Toba (1977), who argued that for very short, strongly forced wind-wave conditions, shear stress is the dominant mechanism for transmitting the atmospheric wind stress into the water motion – waves and surface drift currents. In strong contrast, other authors have more recently observed very substantial normal stress contributions on the air side. The availability of PIV and associated image technology now permits a timely re-examination of the results of Okuda et al., which have been influential in shaping present perceptions of the physics of this dynamically important region. The PIV technique used in the present study overcomes many of the inherent shortcomings of the hydrogen bubble measurements, and allows reliable determination of the fluid velocity and shear within 200 μm of the instantaneous wind-driven air–water interface.The results obtained in this study are not in accord with the conclusions of Okuda et al. that the tangential stress component dominates the wind stress. It is found that prior to the formation of wind waves, the tangential stress contributes the entire wind stress, as expected. With increasing distance downwind, the mean tangential stress level decreases marginally, but as the wave field develops, the total wind stress increases significantly. Thus, the wave form drag, represented by the difference between the total wind stress and the mean tangential stress, also increases systematically with wave development and provides the major proportion of the wind stress once the waves have developed beyond their early growth stage. This scenario reconciles the question of relative importance of normal and tangential stresses at an air–water interface. Finally, consideration is given to the extrapolation of these detailed laboratory results to the field, where the present findings suggest that the sea surface is unlikely to become fully aerodynamically rough, at least for moderate to strong winds.
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16

Madarász, Ádám, Peter J. Rossky, and László Turi. "Excess electron relaxation dynamics at water/air interfaces." Journal of Chemical Physics 126, no. 23 (June 21, 2007): 234707. http://dx.doi.org/10.1063/1.2741514.

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17

Wan, Jiamin, and Tetsu K. Tokunaga. "Partitioning of Clay Colloids at Air–Water Interfaces." Journal of Colloid and Interface Science 247, no. 1 (March 2002): 54–61. http://dx.doi.org/10.1006/jcis.2001.8132.

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18

McGillivray, Duncan J., Jitendra P. Mata, John W. White, and Johann Zank. "Nano- and Microstructure of Air/Oil/Water Interfaces†." Langmuir 25, no. 7 (April 7, 2009): 4065–69. http://dx.doi.org/10.1021/la802865z.

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19

Rodriguez, Javier, and Daniel Laria. "Surface Behavior ofN-Dodecylimidazole at Air/Water Interfaces." Journal of Physical Chemistry C 111, no. 2 (January 2007): 908–15. http://dx.doi.org/10.1021/jp0650883.

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20

Yiapanis, George, Adam Joseph Makarucha, Julia S. Baldauf, and Matthew T. Downton. "Simulations of graphitic nanoparticles at air–water interfaces." Nanoscale 8, no. 47 (2016): 19620–28. http://dx.doi.org/10.1039/c6nr06475b.

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21

Rao, Yi, Nicholas J. Turro, and Kenneth B. Eisenthal. "Water Structure at Air/Acetonitrile Aqueous Solution Interfaces." Journal of Physical Chemistry C 113, no. 32 (July 6, 2009): 14384–89. http://dx.doi.org/10.1021/jp902933e.

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22

Trigg, Ben J., Chiu Fan Lee, David J. Vaux, and Létitia Jean. "The air–water interface determines the outcome of seeding during amyloidogenesis." Biochemical Journal 456, no. 1 (October 24, 2013): 67–80. http://dx.doi.org/10.1042/bj20130605.

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Amyloidogenesis kinetics display inter-dependent catalytic effects of hydrophobic–hydrophilic interfaces (e.g. air–water interface) and seeding with preformed intermediates. These effects are consistent with monomer lateral sequestration on fibrillar seeds. Studying seeding in an interfacial context is crucial to understand amyloidogenesis in vivo.
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23

Hentrich, Doreen, Mathias Junginger, Michael Bruns, Hans G. Börner, Jessica Brandt, Gerald Brezesinski, and Andreas Taubert. "Interface-controlled calcium phosphate mineralization: effect of oligo(aspartic acid)-rich interfaces." CrystEngComm 17, no. 36 (2015): 6901–13. http://dx.doi.org/10.1039/c4ce02274b.

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The phase behavior of an amphiphilic block copolymer based on a poly(aspartic acid) hydrophilic block and a poly(n-butyl acrylate) hydrophobic block was investigated at the air–water and air–buffer interface.
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24

Bettini, Simona, Angelo Santino, Gabriele Giancane, and Ludovico Valli. "Reconstituted oil bodies characterization at the air/water and at the air/oil/water interfaces." Colloids and Surfaces B: Biointerfaces 122 (October 2014): 12–18. http://dx.doi.org/10.1016/j.colsurfb.2014.06.044.

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25

Wang, Chang-Wei, Hui-Ping Ding, Guo-Qing Xin, Xiao Chen, Yong-Ill Lee, Jingcheng Hao, and Hong-Guo Liu. "Silver nanoplates formed at the air/water and solid/water interfaces." Colloids and Surfaces A: Physicochemical and Engineering Aspects 340, no. 1-3 (May 2009): 93–98. http://dx.doi.org/10.1016/j.colsurfa.2009.03.003.

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26

Chanda, S., D. Das, J. Das, and K. Ismail. "Adsorption characteristics of sodium dodecylsulfate and cetylpyridinium chloride at air/water, air/formamide and air/water–formamide interfaces." Colloids and Surfaces A: Physicochemical and Engineering Aspects 399 (April 2012): 56–61. http://dx.doi.org/10.1016/j.colsurfa.2012.02.024.

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27

Denneman, Arthur I. M., Guy G. Drijkoningen, David M. J. Smeulders, and Kees Wapenaar. "Reflection and transmission of waves at a fluid/porous‐medium interface." GEOPHYSICS 67, no. 1 (January 2002): 282–91. http://dx.doi.org/10.1190/1.1451800.

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We study the wave properties at a fluid/porous‐medium interface by using newly derived closed‐form expressions for the reflection and transmission coefficients. We illustrate the usefulness of these relatively simple expressions by applying them to a water/porous‐medium interface (with open‐pore or sealed‐pore boundary conditions), where the porous medium consists of (1) a water‐saturated clay/silt layer, (2) a water‐saturated sand layer, (3) an air‐filled clay/silt layer, or (4) an air‐filled sand layer. We observe in the frequency range 5 Hz–20 kHz that the fast P‐wave and S‐wave velocities in the four porous materials are indistinguishable from the corresponding frequency‐independent ones calculated using Gassmann relations. Consequently, for these frequencies we would expect the reflection and transmission coefficients for the four water/porous‐medium interfaces to be similar to the ones for corresponding interfaces between water and effective elastic media (described by Gassmann wave velocities). This expectation is not fulfilled in the case of an interface between water and an air‐filled porous layer with open pores. A close examination of the expressions for the reflection and transmission coefficients shows that this unexpected result is because of the large density difference between water and air.
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28

Poonia, Monika, V. Manjuladevi, and R. K. Gupta. "Ultrathin film of carboxylated graphene at air-water and air-solid interfaces." Surfaces and Interfaces 13 (December 2018): 37–45. http://dx.doi.org/10.1016/j.surfin.2018.07.007.

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29

Nayak, Alpana, K. A. Suresh, Santanu Kumar Pal, and Sandeep Kumar. "Films of Novel Mesogenic Molecules at Air−Water and Air−Solid Interfaces." Journal of Physical Chemistry B 111, no. 38 (September 2007): 11157–61. http://dx.doi.org/10.1021/jp073196z.

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30

Zhong, J., M. Kumar, J. M. Anglada, M. T. C. Martins-Costa, M. F. Ruiz-Lopez, X. C. Zeng, and Joseph S. Francisco. "Atmospheric Spectroscopy and Photochemistry at Environmental Water Interfaces." Annual Review of Physical Chemistry 70, no. 1 (June 14, 2019): 45–69. http://dx.doi.org/10.1146/annurev-physchem-042018-052311.

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The air–water interface is ubiquitous in nature, as manifested in the form of the surfaces of oceans, lakes, and atmospheric aerosols. The aerosol interface, in particular, can play a crucial role in atmospheric chemistry. The adsorption of atmospheric species onto and into aerosols modifies their concentrations and chemistries. Moreover, the aerosol phase allows otherwise unlikely solution-phase chemistry to occur in the atmosphere. The effect of the air–water interface on these processes is not entirely known. This review summarizes recent theoretical investigations of the interactions of atmosphere species with the air–water interface, including reactant adsorption, photochemistry, and the spectroscopy of reactants at the water surface, with an emphasis on understanding differences between interfacial chemistries and the chemistries in both bulk solution and the gas phase. The results discussed here enable an understanding of fundamental concepts that lead to potential air–water interface effects, providing a framework to understand the effects of water surfaces on our atmosphere.
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31

Hórvölgyi, Z., S. Németh, and J. H. Fendler. "Spreading of hydrophobic silica beads at water—air interfaces." Colloids and Surfaces A: Physicochemical and Engineering Aspects 71, no. 3 (June 1993): 327–35. http://dx.doi.org/10.1016/0927-7757(93)80048-j.

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32

Ma, Jun, Jin Jiang, SuYan Pang, and Jin Guo. "Adsorptive Fractionation of Humic Acid at Air−Water Interfaces." Environmental Science & Technology 41, no. 14 (July 2007): 4959–64. http://dx.doi.org/10.1021/es070238o.

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33

Wan, Jiamin, and Tetsu K. Tokunaga. "Measuring Partition Coefficients of Colloids at Air−Water Interfaces." Environmental Science & Technology 32, no. 21 (November 1998): 3293–98. http://dx.doi.org/10.1021/es980228a.

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34

Roland, C. M., M. J. Zuckermann, and A. Georgallas. "Phase transitions in phospholipid monolayers at air–water interfaces." Journal of Chemical Physics 86, no. 10 (May 15, 1987): 5852–58. http://dx.doi.org/10.1063/1.452515.

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35

Cieplak, Marek, Daniel B. Allan, Robert L. Leheny, and Daniel H. Reich. "Proteins at Air–Water Interfaces: A Coarse-Grained Model." Langmuir 30, no. 43 (October 24, 2014): 12888–96. http://dx.doi.org/10.1021/la502465m.

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36

Chung, Judy B., Robert E. Hannemann, and Elias I. Franses. "Surface analysis of lipid layers at air/water interfaces." Langmuir 6, no. 11 (November 1990): 1647–55. http://dx.doi.org/10.1021/la00101a005.

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37

Cieplak, Marek, and Grzegorz Nawrocki. "Proteins Near Solid Surfaces and at Air-Water Interfaces." Biophysical Journal 110, no. 3 (February 2016): 645a. http://dx.doi.org/10.1016/j.bpj.2015.11.3454.

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38

Rucker, George, Xiong Yu, and Liqun Zhang. "Molecular dynamics investigation on n-alkane-air/water interfaces." Fuel 267 (May 2020): 117252. http://dx.doi.org/10.1016/j.fuel.2020.117252.

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39

Bochenek, Steffen, Cathy E. McNamee, Michael Kappl, Hans-Juergen Butt, and Walter Richtering. "Interactions between a responsive microgel monolayer and a rigid colloid: from soft to hard interfaces." Physical Chemistry Chemical Physics 23, no. 31 (2021): 16754–66. http://dx.doi.org/10.1039/d1cp01703a.

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We investigated the interaction between microgel monolayers at the air–water interface and a hard colloid in water. Our results show that microgel monolayers change from soft to hard repulsive interfaces when the VPTT is exceeded.
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40

Occhiello, E., M. Morra, G. Morini, F. Garbassi, and P. Humphrey. "Oxygen-plasma-treated polypropylene interfaces with air, water, and epoxy resins: Part I. Air and water." Journal of Applied Polymer Science 42, no. 2 (January 20, 1991): 551–59. http://dx.doi.org/10.1002/app.1991.070420228.

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41

Theodoratou, Antigoni, Ulrich Jonas, Benoit Loppinet, Thomas Geue, René Stangenberg, Dan Li, Rüdiger Berger, and Dimitris Vlassopoulos. "Photoswitching the mechanical properties in Langmuir layers of semifluorinated alkyl-azobenzenes at the air–water interface." Physical Chemistry Chemical Physics 17, no. 43 (2015): 28844–52. http://dx.doi.org/10.1039/c5cp04242a.

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42

Pezzotti, Simone, and Marie-Pierre Gaigeot. "Spectroscopic BIL-SFG Invariance Hides the Chaotropic Effect of Protons at the Air-Water Interface." Atmosphere 9, no. 10 (October 11, 2018): 396. http://dx.doi.org/10.3390/atmos9100396.

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The knowledge of the water structure at the interface with the air in acidic pH conditions is of utmost importance for chemistry in the atmosphere. We shed light on the acidic air-water (AW) interfacial structure by DFT-MD simulations of the interface containing one hydronium ion coupled with theoretical SFG (Sum Frequency Generation) spectroscopy. The interpretation of SFG spectra at charged interfaces requires a deconvolution of the signal into BIL (Binding Interfacial Layer) and DL (Diffuse Layer) SFG contributions, which is achieved here, and hence reveals that even though H 3 O + has a chaotropic effect on the BIL water structure (by weakening the 2D-HBond-Network observed at the neat air-water interface) it has no direct probing in SFG spectroscopy. The changes observed experimentally in the SFG of the acidic AW interface from the SFG at the neat AW are shown here to be solely due to the DL-SFG contribution to the spectroscopy. Such BIL-SFG and DL-SFG deconvolution rationalizes the experimental SFG data in the literature, while the hydronium chaotropic effect on the water 2D-HBond-Network in the BIL can be put in perspective of the decrease in surface tension at acidic AW interfaces.
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43

Kahan, T. F., R. Zhao, and D. J. Donaldson. "Hydroxyl radical reactivity at the air-ice interface." Atmospheric Chemistry and Physics 10, no. 2 (January 26, 2010): 843–54. http://dx.doi.org/10.5194/acp-10-843-2010.

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Abstract. Hydroxyl radicals are important oxidants in the atmosphere and in natural waters. They are also expected to be important in snow and ice, but their reactivity has not been widely studied in frozen aqueous solution. We have developed a spectroscopic probe to monitor the formation and reactions of hydroxyl radicals in situ. Hydroxyl radicals are produced in aqueous solution via the photolysis of nitrite, nitrate, and hydrogen peroxide, and react rapidly with benzene to form phenol. Similar phenol formation rates were observed in aqueous solution and bulk ice. However, no reaction was observed at air-ice interfaces, or when bulk ice samples were crushed prior to photolysis to increase their surface area. We also monitored the heterogeneous reaction between benzene present at air-water and air-ice interfaces with gas-phase OH produced from HONO photolysis. Rapid phenol formation was observed on water surfaces, but no reaction was observed at the surface of ice. Under the same conditions, we observed rapid loss of the polycyclic aromatic hydrocarbon (PAH) anthracene at air-water interfaces, but no loss was observed at air-ice interfaces. Our results suggest that the reactivity of hydroxyl radicals toward aromatic organics is similar in bulk ice samples and in aqueous solution, but is significantly suppressed in the quasi-liquid layer (QLL) that exists at air-ice interfaces.
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44

Kahan, T. F., R. Zhao, and D. J. Donaldson. "Hydroxyl radical reactivity at the air-ice interface." Atmospheric Chemistry and Physics Discussions 9, no. 5 (October 5, 2009): 20881–911. http://dx.doi.org/10.5194/acpd-9-20881-2009.

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Abstract. Hydroxyl radicals are important oxidants in the atmosphere and in natural waters. They are also expected to be important in snow and ice, but their reactivity has not been widely studied in frozen aqueous solution. We have developed a spectroscopic probe to monitor the formation and reactions of hydroxyl radicals in situ. Hydroxyl radicals are produced in aqueous solution via the photolysis of nitrite, nitrate, and hydrogen peroxide, and react rapidly with benzene to form phenol. Similar phenol formation rates were observed in aqueous solution and bulk ice. However, no reaction was observed at the air-ice interface, or when bulk ice samples were crushed prior to photolysis to increase their surface area. We also monitored the heterogeneous reaction between benzene present at air-water and air-ice interfaces with gas-phase OH produced from HONO photolysis. Rapid phenol formation was observed on water surfaces, but no reaction was observed at the surface of ice. Under the same conditions, we observed rapid loss of the polycyclic aromatic hydrocarbon (PAH) anthracene at the air-water interface, but no loss was observed at the air-ice interface. Our results suggest that the reactivity of hydroxyl radicals toward aromatic organics is similar in bulk ice samples and in aqueous solution, but is significantly suppressed in the quasi-liquid layer (QLL) that exists at the air-ice interface.
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45

Rühs, Patrick A., R. Fredrik Inglis, and Peter Fischer. "Interfacial Rheology of Bacterial Biofilms at Air/Water and Oil/Water Interfaces." CHIMIA International Journal for Chemistry 68, no. 4 (April 30, 2014): 273. http://dx.doi.org/10.2533/chimia.2014.273.

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46

Dominguez, H., A. M. Smondyrev, and M. L. Berkowitz. "Computer Simulations of Phosphatidylcholine Monolayers at Air/Water and CCl4/Water Interfaces." Journal of Physical Chemistry B 103, no. 44 (November 1999): 9582–88. http://dx.doi.org/10.1021/jp991352z.

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47

McCaffrey, Debra L., Son C. Nguyen, Stephen J. Cox, Horst Weller, A. Paul Alivisatos, Phillip L. Geissler, and Richard J. Saykally. "Mechanism of ion adsorption to aqueous interfaces: Graphene/water vs. air/water." Proceedings of the National Academy of Sciences 114, no. 51 (August 21, 2017): 13369–73. http://dx.doi.org/10.1073/pnas.1702760114.

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48

Teschke, O., and E. F. de Souza. "Water molecule clusters measured at water/air interfaces using atomic force microscopy." Physical Chemistry Chemical Physics 7, no. 22 (2005): 3856. http://dx.doi.org/10.1039/b511257e.

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49

Balashev, K., A. Bois, J. E. Proust, Tz Ivanova, I. Petkov, S. Masuda, and I. Panaiotov. "Comparative Study of Polyacryloylacetone Monolayers at Dichloromethane−Water and Air−Water Interfaces." Langmuir 13, no. 20 (October 1997): 5362–67. http://dx.doi.org/10.1021/la9607058.

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50

Truong, Vu N. T., Xuming Wang, Liem X. Dang, and Jan D. Miller. "Interfacial Water Features at Air–Water Interfaces as Influenced by Charged Surfactants." Journal of Physical Chemistry B 123, no. 10 (February 15, 2019): 2397–404. http://dx.doi.org/10.1021/acs.jpcb.9b01246.

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