An improved method for determining the susceptibility ofRhizoglyphus robini andR. setosus (Acarina:Acaridae) to pesticides

A dramatic increase in the surface tension of water with decreasing temperature in the supercooled liquid region has appeared as one of the many anomalies of water. This claimed anomaly characterized by the second inflection point at about +1.5 °C was observed in older surface tension data and was partially supported by some molecular simulations and theoretical considerations. In this study, two independent sets of experimental data for the surface tension of water in the temperature range between +33 and -25 °C are reported. The two data sets are mutually consistent, and they lie on a line smoothly extrapolating from the stable region. No second inflection point and no other anomalies in the course of the surface tension were observed. The new data lies very close to the extrapolated IAPWS correlation for the surface tension of ordinary water, which hence can be recommended for use, e.g., in atmospheric modeling.

Measurements of the surface tension of supercooled water down to -25 °C have been reported recently (Hrubý et al. J. Phys. Chem. Lett. 2014, 5, 425-428). These experiments did not show any anomalous temperature dependence of the surface tension of supercooled water reported by some earlier measurements and molecular simulations. In the present work, this finding is confirmed using a counterpressure capillary rise method (the counterpressure method) as well as through the use of the classical capillary rise method (the height method). In the counterpressure method, the liquid meniscus inside the vertical capillary tube was kept at a fixed position with an in-house developed helium distribution setup. A preset counterpressure was applied to the liquid meniscus when its temperature changed from a reference temperature (30 °C) to the temperature of interest. The magnitude of the counterpressure was adjusted such that the meniscus remained at the same height, thus compensating the change of the surface tension. One advantage of the counterpressure method over the height method consists of avoiding the uncertainty due to a possible variation of the capillary diameter along its length. A second advantage is that the equilibration time due to the capillary flow of the highly viscous supercooled water can be shortened. For both the counterpressure method and the height method, the actual results are relative values of surface tension with respect to the surface tension of water at the reference temperature. The combined relative standard uncertainty of the relative surface tensions is less than or equal to 0.18%. The new data between -26 and +30 °C lie close to the IAPWS correlation for the surface tension of ordinary water extrapolated below 0.01 °C and do not exhibit any anomalous features.

The surface tension of water is suspected to show a substantial increase at low temperatures, which is considered to be one of the many anomalies of water. The second inflection point (SIP) anomaly, originally claimed to be at around -8 °C, was experimentally refuted down to -25 °C by Hrubý et al. (J. Phys. Chem. Lett. 2014, 5, 425-428). Recent molecular simulations predict the SIP anomaly near or even below the homogeneous freezing limit of around -38 °C. To contribute to an ongoing discussion about the SIP anomaly, new experiments focused on extreme levels of supercooling were carried out in this study. Unique experimental data down to -31.4 °C were collected using two measuring techniques based on the capillary rise method. A significant deviation from the extrapolated IAPWS formulation R1-76(2014) for surface tension of ordinary water was detected below -20 °C. Contrary to previous data, new experiments provide room for an anomaly in the course of surface tension in the deeply supercooled region.

In this work, non-reactive molecular dynamic simulations were conducted to determine the surface tension of water as a function of the concentration of the dissolved gaseous molecules (O2), which would in turn help to predict the pressure inside the nanobubbles under supersaturation conditions. Knowing the bubble pressure is a prerequisite for understanding the mechanisms behind the spontaneous combustion of the H2/O2 gases inside the nanobubbles. First, the surface tension of pure water was determined using the planar interface method and the Irving and Kirkwood formula. Next, the surface tension of water containing four different supersaturation concentrations (S) of O2 gas molecules was computed considering the curved interface of a nanobubble. The surface tension of water was found to decrease with an increase in the supersaturation ratio or the concentration of the dissolved O2 gas molecules.

The surface tensions of water and aqueous lithium bromide (LiBr) with 2-ethyl-1-hexanol (2EH) and 1-octanol were measured using Wilhelmy plate method, and the oscillation of surface tension under the open condition for LiBr solution was observed. The dynamic surface tensions of water and LiBr solution in the presence of the 2EH and 1-octanol vapor were measured in this paper. The results showed that the additives vapor could obviously affect surface tension. For water, the dynamic surface tension was also affected by the mass of the tested liquid; however, for LiBr solution, the dynamic surface tension was not related to the mass of the tested solution. According to the experimental results, the hypothesis that surface tension varies linearly with the surface excess concentration is advanced, which could overcome the limit of Gibbs equation. The equations of surface absorption and desorption are modified, the units of the adsorption coefficient and desorption coefficient are unified; the effects of the liquid and vapor of additive on the surface tension are unified; the theoretical relations of the static surface tension and dynamic surface tension with the relative contents of the liquid and vapor of additive are obtained under the combined actions of them; the theoretical equations are validated by the experiments results.

The Variation of Surface Tension and Contact Angle under Applied Pressure of Dissolved Gases, and the Effects of These Changes on the Rate of Bubble Nucleation

Abstract. Surface tension of ternary solution of sodium chloride, succinic acid and water was measured as a function of both composition and temperature by using the capillary rise technique. Both sodium chloride and succinic acid are found in atmospheric aerosols, the former being main constituent of marine aerosol. Succinic acid was found to decrease the surface tension of water already at very low concentrations. Sodium chloride increased the surface tension linearly as a function of the concentration. Surface tensions of both binary solutions agreed well with the previous measurements. Succinic acid was found to lower the surface tension even if sodium chloride is present, indicating that succinic acid, as a surface active compound, tends to concentrate to the surface. An equation based on thermodynamical relations was fitted to the data and extrapolated to the whole concentration range by using estimated surface tensions for pure compounds. As a result, we obtained an estimate of surface tensions beyond solubility limits in addition to a fit to the experimental data. The parameterization can safely be used at temperatures from 10 to 30°C. These kinds of parameterizations are important for example in atmospheric nucleation models. To investigate the influence of surface tension on cloud droplet activation, the surface tension parameterization was included in an adiabatic air parcel model. Usually in cloud models the surface tension of pure water is used. Simulations were done for characteristic marine aerosol size distributions consisting of the considered ternary mixture. We found that by using the surface tension of pure water, the amount of activated particles is underestimated up to 8% if particles contain succinic acid and overestimated it up to 8% if particles contain only sodium chloride. The surface tension effect was found to increase with increasing updraft velocity.

Variation of surface tension coefficient σ of distilled water under high-energy impact (hydrodynamic cavitation) was studied by the ring separation method. Force impacts on surface tension of water have been studied experimentally. Conditions have been found under which the surface tension coefficient σ decreases to 20%. The paper explains the produced results on the basis of cluster theory of water structure. The experimentally produced relaxation time of the surface tension of cavitation-activated distilled water to initial value has been found to be 3.5 hours.

The investigation about surface tension of water used for preparation of pesticide solutions reveals it is quite diverse and changeable without any logical correlation towards location, time, and type of water source. Moreover, spraying with solutions with lower surface tension give bigger flow rates due to the lower resistance of fluid to the nozzles. The conducted trials show that plant surfaces with more rough texture require to be sprayed with pesticide solutions with lower surface tension. The wax content of the surfaces has no significant impact on surface tension requirement.

The surface tension of water calculated from a random network model

Surface Tension and Dynamic Contact Angle of Water in Thin Quartz Capillaries

Surface tension of pure water and aqueous lithium bromide with 2-ethyl-hexanol

An experimental self-etching dentin primer, prepared by dissolving an acidic monomer, methacryloxyethyl succinate (MES), dimethacryloxyethyl phosphate (DMEP) or tertiarybutyl acrylamide sulfonic acid (TBAS), in an aqueous solution of 2.9M 2-hydroxyethyl methacrylate (HEMA), has been shown to promote adhesion by a bonding agent between a composite resin and dentin. To clarify the mechanism of this promotion we examined the effects of acidic monomers on dentin cleansing, surface tension of water and hypotonic hemolysis of rat erythrocytes. In scanning electron microscope observation of the dentin surface, the smear layer remained slightly evident after MES-HEMA treatment. DMEP-HEMA or TBAS-HEMA caused complete removal of the smear layer, and openings of dentinal tubules were clearly evident. MES and DMEP, 1×10-6 M and 1×10-4 M, respectively, decreased the surface tension of distilled water (72 dyne/cm) . The surface tension depression by 0.3M HEMA was apparently not further affected by MES, DMEP or TBAS at 1×10-7 to 1×10-2M. The osmotic pressure of hypotonic buffer was increased by MES, DMEP, TBAS and HEMA at concentrations greater than 1×10-2M. The hypotonic hemolysis of erythrocytes was inhibited by MES and TBAS at 4×10-3 to 1×10-2M and by HEMA at 4×10-1M. DMEP promoted hypotonic hemolysis at 4×10-5 to 1×10-4M, but caused inhibition in the concentration range of 4×10-4 to 1×10-3M. The protective effect of acidic monomers on the erythrocytes was promoted by the presence of 0.1 M HEMA, while DMEP at 1×10-2 M showed only a lytic effect. These results suggest that the mechanism of promotion of the adhesive ability of a bonding agent by self-etching dentin primers containing these acidic monomers is related to the increased surface activity of water and membrane stability of erythrocytes, since these effects of acidic monomers might be caused by the reduction in surface tension of secretion from dentin and inhibition of secretion from dentinal tubules.

Surface tension of supercooled water is a fundamental property in various scientific processes. In this study, we perform molecular dynamics simulations with the TIP4P-2005 model to investigate the surface tension of supercooled water down to 220K. Our results show a second inflection point (SIP) in the surface tension at temperature TSIP ≈ 267.5 ± 2.3K. Using an extended IAPWS-E functional fit for the water surface tension, we calculate the surface excess internal-energy and entropy terms of the excess Helmholtz free energy. Similar to prior studies [Wang et al., Phys. Chem. Chem. Phys. 21, 3360 (2019); Gorfer et al., J. Chem. Phys. 158, 054503 (2023)], our results show that the surface tension is governed by two driving forces: a surface excess entropy change above the SIP and a surface excess internal-energy change below it. We study hydrogen-bonding near the SIP because it is the main cause of water's anomalous properties. With decreasing temperature, our results show that the entropy contribution to the surface tension reaches a maximum slightly below the SIP and then decreases. This is because the number of hydrogen bonds increases more slowly below the SIP. Moreover, the strengths and lifetimes of the hydrogen bonds also rise dramatically below the SIP, causing the internal-energy term to dominate the excess surface free energy. Thus, the SIP in the surface tension of supercooled TIP4P-2005 water is associated with an increase in the strengths and lifetimes of hydrogen bonds, along with a decrease in the formation rate (#/K) of new hydrogen bonds.

The surface tension and surface energy of water is calculated using the Fowler approximation. The direct Monte Carlo integration and the calculation using the atom-atom pair correlation funtions are reported. The configuration interaction pair potential was used. The results show that feasible agreement with the experiment can be obtained.