Soil volumetric water content (θ) is a parameter describing one of the most important factors conditioning proper plant growth. Monitoring soil moisture is of particular importance in the rational use of water resources for irrigation, especially during periods of water scarcity. This paper presents a method of measuring soil moisture in the vicinity of the plant root system by means of a probe designed to be mounted on a mobile device used for precise plant irrigation. Due to the specific field conditions of the measurement, the design of the probe was proposed as a monopole antenna. Electromagnetic simulations of the probe were carried out with Ansys HFSS software to optimise its dimensions. Then a prototype of the probe was manufactured to conduct laboratory measurements with the use of a vector network analyser (VNA) working in the 20 kHz to 8 GHz frequency range. The VNA analyser was configured to work in the time-domain reflectometry (TDR) mode. From measurements of the time distance between reflections from the probe’s elements it is possible to calculate the bulk dielectric permittivity of the soil surrounding the probe. Next, based on commonly used soil moisture dielectric calibrations one can determine θ of the soil sample. The paper presents simulation results and laboratory tests of an antenna probe. Due to its tough and durable design, this type of probe gives the possibility of easy application in field conditions, which makes it especially suitable for mechanically demanding measurement systems. As the sensitivity zone is comparatively large, this probe is well-suited to measuring soil moisture in the vicinity of the plant root system.

This paper presents dielectric measurements of talc, glass beads, and their mixtures under different moisture and salinity levels. The measurements were conducted using a prototype seven-rod probe (15 mm long central rod) connected to a single port of vector network analyzer. The samples were moistened with distilled water and KCl solutions in order to obtain six different moisture content levels. The complex dielectric permittivity was determined from vector network analyzer reflection-coefficient measurements based on the open-water-liquid calibration procedure. Next, the fitting of volumetric water content–real part of dielectric permittivity calibration curves was performed for each material at selected frequencies, and the obtained relations were compared with well-known calibration equations. Additionally, a salinity index for the tested materials was calculated. It was concluded that pure talc is not an optimal material for the calibration and verification of dielectric methods. The calibration curves obtained for glass beads and the mixtures of glass beads with talc gave results close to well-known reference calibration functions. Additionally, the addition of talc caused the data points to be less scattered. Moreover, the values of the salinity index for the tested materials were in a good agreement with literature data for sand. The obtained results indicated that glass beads with the addition of talc can be used as a reference material for the calibration and verification of dielectric methods and devices for soil moisture measurement.

This paper presents a novel seven-rod sensor used for time-domain reflectometry (TDR) and frequency-domain reflectometry (FDR) measurements of soil water content in a well-defined sample volume. The probe directly measures the complex dielectric permittivity spectrum and for this purpose requires three calibration media: air, water, and ethanol. Firstly, electromagnetic simulations were used to study the influence of the diameter of a container on the sensitivity zone of the probe with respect to the measured calibration media and isopropanol as a verification liquid. Next, the probe was tested in three soils—sandy loam and two silt loams—with six water contents from air-dry to saturation. The conversion from $S_{11}$ parameters to complex dielectric permittivity from vector network analyzer (VNA) measurements was obtained using an open-ended liquid procedure. The simulation and measurement results for the real part of the isopropanol dielectric permittivity obtained from four containers with different diameters were in good agreement with literature data up to 200 MHz. The real part of the dielectric permittivity was extracted and related to the moisture of the tested soil samples. Relations between the volumetric water content and the real part of the dielectric permittivity (by FDR) and apparent dielectric permittivity (by TDR) were compared with Topp’s equation. It was concluded that the best fit to Topp’s equation was observed in the case of a sandy loam. Data calculated according to the equation proposed by Malicki, Plagge, and Roth gave results closer to Topp’s calibration. The obtained results indicated that the seven-rod probe can be used to accurately measure of the dielectric permittivity spectrum in a well-defined sample volume of about 8 cm³ in the frequency range from 20 MHz to 200 MHz.

Achieving control over structure of adsorbed chiral overlayers is an important objective in the fabrication of functional surfaces with predefined optical, adsorptive and catalytic properties. In this contribution we explore the surface-confined segregation of enantiomers of model prochiral molecules that is triggered by continuous breaking of their orientational symmetry and which leads to the creation of extended homochiral domains. To that end we use the lattice gas Monte Carlo method combined with a coarse-grained representation of prototype prochiral molecules comprising a few identical segments arranged in different shapes. The adsorbed enantiomers are assumed to interact via short-ranged attractive segment–segment interaction potential limited to nearest neighbors on a square lattice. Additionally, to account for the external asymmetric input which breaks the orientational symmetry (e.g. electric or magnetic field) we assume that the prochiral molecules are able to couple with continuously changed directional field parallel to the surface. It is demonstrated that by fine tuning of the external field, which orients the molecules in one direction, it is possible to induce a complete segregation of the adsorbed enantiomers. The effect of size and shape of the molecules on the extent of the corresponding 2D separations is also assessed. The theoretical findings of our study can be helpful in developing strategies for 2D chiral separations in which external stimuli are used and they can give hints for design and fabrication of new responsive materials.