Behavior of two phenyl urea herbicides in clayey soils and effect of alternating dry-wet conditions on their availability

Adsorption and mobility of linuron (3-(3,4-dichlorophenyl)-1-methoxy-1-methylurea) and diuron (3-(3,4-dichlorophenyl)-1, 1-dimethylurea) were studied in clayey soils from the Gharb area (Morocco). Soils A and B were planted with sun flower (Helianthus annuus) while soil C was planted with sugar cane (Saccharum offcinarum). Adsorption was studied for linuron in soils A and B, while mobility was studied only in soil B. Adsorption data were found to fit the Freundlich equation with correlation coefficients r2 > 0.9. Freundlich coefficients (Kf, nf) were in agreement with L and S isotherm types for soils A and B, respectively. Values of Koc (195 and 102) indicate moderate adsorption. Desorption isotherms for linuron showed hysteresis for both soils. The pesticide would be more bound to soil A (H = 8.44) than to soil B (H = 4.01). The effect of alternating wet and dry conditions was tested for soils A and B. Results showed that retention would increase in soil subject to an additional wet and dry cycle. In the case of diuron isotherm was of type L in soil C. Desorption was noticeable at high concentrations and tended to decrease when concentrations diminished. Mobility of linuron was tested in polyvinyle chloride (PVC) columns, which received different treatments before their percolation. The pesticide was more mobile in a previously saturated column. In columns subject to a drying step after saturation with water, linuron mobility was greatly reduced.     

A multi-variate statistical model integrating passive sampler and meteorology data to predict the frequency distributions of hourly ambient ozone (O3) concentrations

A multi-variate, non-linear statistical model is described to simulate passive O3 sampler data to mimic the hourly frequency distributions of continuous measurements using climatologic O3 indicators and passive sampler measurements. The main meteorological parameters identified by the model were, air temperature, relative humidity, solar radiation and wind speed, although other parameters were also considered. Together, air temperature, relative humidity and passive sampler data by themselves could explain 62.5-67.5% (R(2)) of the corresponding variability of the continuously measured O3 data. The final correlation coefficients (r) between the predicted hourly O3 concentrations from the passive sampler data and the true, continuous measurements were 0.819-0.854, with an accuracy of 92-94% for the predictive capability. With the addition of soil moisture data, the model can lead to the first order approximation of atmospheric O3 flux and plant stomatal uptake. Additionally, if such data are coupled to multi-point plant response measurements, meaningful cause-effect relationships can be derived in the future.     

Behavior of Two Phenyl Urea Herbicides in Clayey Soils and Effect of Alternating Dry-Wet Conditions on their Availability

Adsorption and mobility of linuron (3-(3,4-dichlorophenyl)-1-methoxy-1-methylurea) and diuron (3-(3,4-dichlorophenyl)-1, 1-dimethylurea) were studied in clayey soils from the Gharb area (Morocco). Soils A and B were planted with sun flower (Helianthus annuus) while soil C was planted with sugar cane (Saccharum offcinarum). Adsorption was studied for linuron in soils A and B, while mobility was studied only in soil B. Adsorption data were found to fit the Freundlich equation with correlation coefficients r² > 0.9. Freundlich coefficients (K_f, n_f) were in agreement with L and S isotherm types for soils A and B, respectively. Values of K_oc (195 and 102) indicate moderate adsorption. Desorption isotherms for linuron showed hysteresis for both soils. The pesticide would be more bound to soil A (H = 8.44) than to soil B (H = 4.01). The effect of alternating wet and dry conditions was tested for soils A and B. Results showed that retention would increase in soil subject to an additional wet and dry cycle. In the case of diuron isotherm was of type L in soil C. Desorption was noticeable at high concentrations and tended to decrease when concentrations diminished. Mobility of linuron was tested in polyvinyle chloride (PVC) columns, which received different treatments before their percolation. The pesticide was more mobile in a previously saturated column. In columns subject to a drying step after saturation with water, linuron mobility was greatly reduced.     

Influence of the inlet air in efficiency of photocatalytic devices for mineralization of VOCs in air-conditioning installations

Nowadays, a large proportion of photocatalytic oxidation (PCO) devices are being implemented in heating, ventilation and air-conditioning systems. However, no systematic studies have been carried out regarding the influence of inlet air preconditioning. To analyse the impact of the inlet air-conditions into photocatalytic efficiency, a simulated air-conditioning duct with flowing gas through inside was designed. Isobutylene was chosen as the target VOCs. The concentration in the gas phase was monitored using a photoionization detector. The influence of flow rate, relative humidity and temperature on the VOC removal efficiency was analysed. Experimental results were presented in terms of gas-removal efficiency (η) and clean air delivery rate (CADR) and analysed on a kinetic basis. From them, the weight of each parameter in the global process has been determined, from bigger to smaller contribution, flow>>temperature>relative humidity. Also, the relevance of the inlet air conditions has been illustrated in a model room in order to determinate the time necessary to obtain a threshold value accomplishing with enough air quality and the energy consumption of the device. Additionally, the photocatalytic decontamination has been assimilated to the “air exchange rate”, a parameter commonly used in indoor air quality studies. The results show that preconditioning of air can improve the efficiency of photocatalytic devices and bring important energy savings.     

Light scattering characteristics of aerosols as a function of relative humidity: Part I--A comparison of measured scattering and aerosol concentrations using the theoretical models

The Southeastern Aerosol and Visibility Study (SEAVS) was undertaken to characterize the size-dependent composition, thermodynamic properties, and optical characteristics of the ambient atmospheric particles in the southeastern United States. The field portion of the study was carried out from July 15 to August 25, 1995. As part of the study a relative humidity controlled inlet was built to raise or lower the relative humidity to predetermined levels before the aerosol was passed into an integrating nephelometer or particle-sizing device. Five other integrating nephelometers were operated in various configurations, two of which were fitted with a 2.5 microns inlet. Fine particle (< 2.5 microns) samplers were operated to measure concentrations of sulfate, nitrate, and ammonium ions, organic and elemental carbon, and fine soil. Mass size distributions were measured with an eight-stage, single orifice cascade impactor. Four different strategies for estimating scattering were used. First, an externally mixed model with constant specific scattering coefficients, sulfate ion mass interpreted as ammonium bisulfate, and ammonium bisulfate growth as a function of relative humidity, is assumed. Second, an externally mixed aerosol model, assuming constant dry specific scattering but with sulfate ammoniation and associated composition-dependent hygroscopicity explicitly accounted for, is used. Third, an externally mixed aerosol model, but with sulfate ammoniation, associated growth as a function of relative humidity, and sulfate size distributions, is applied. Fourth, an internally mixed aerosol model with measured sulfur size distributions and estimated size distributions for other species is used with the growth characteristics of the mixture being estimated using the Zdanovskii-Stokes-Robinson (ZSR) assumptions. Only ionic species were considered to be hygroscopic. The second, third, and fourth approaches yield similar results with reconstructed scattering comparing quite favorably with measured scattering. Accounting for sulfate ammoniation and associated water uptake was the most important detail in achieving closure between measurements and modeled scattering. In general, differences between estimated scattering, assuming internally or externally mixed models, was small. These same models were used to estimate wet to dry scattering ratios. The R2 for an ordinary least-squares regression between measured and predicted ratios was high (0.71-0.92), and in most cases the scattering ratio was insensitive to modeling assumptions. However, during some sample periods differences between predicted scattering ratios for the different modeling assumptions were as high as 30%.     

Measurements of ammonia concentrations,fluxes and dry deposition velocities to a spruce forest 1991–1995

The dry deposition velocities and fluxes of ammonia have been estimated from measurements of the vertical gradient of ammonia and micrometeorology above a spruce forest in western Jutland, Denmark. Measurements have been made in seven periods, each lasting about one week and covering all seasons and different meteorological situations. Different deposition characteristics were observed, depending on the ammonia concentration and the relative humidity. At conditions with westerly winds, the wind brings air masses from the North Sea with low concentration levels of ammonia to the site, while at conditions with easterly winds, the air have passed central Jutland with large emission areas. Some of the relatively low deposition velocities or emissions were observed during conditions with low ammonia concentration and westerly winds. These observations might relate to a compensation point of the forest, i.e. an ammonia concentration below which the trees and/or the surface emit ammonia due to an equilibrium with the ammonia inside the needles or on the surface. Emission of ammonia was also observed at relatively high ammonia concentration levels (above 2 μg NH₃–N m^-3), mainly during one measuring period characterized by easterly winds with dry conditions and high ammonia concentrations, and the emissions might relate to evaporation from ammonia saturated surfaces or emission from mineralization in the forest soil. In general, relatively high net deposition velocities were observed during conditions with relative humidity above 80% or at ammonia concentrations moderate higher than a given (temperature dependent) compensation point. During stable conditions some observations revealed that the gradient above the canopy not necessarily represents the exchange with the canopy.     

Effects of soil moisture and physical-chemical properties of organic pollutants on vapor-phase transport in the vadose zone

Vapor-phase transport of organic pollutants is one of the important pathways in the distribution and attenuation of volatile organic compounds in the vadose zone. In this study, the impact of vapor-phase partitioning and of the physical-chemical properties of organic pollutants on vapor-phase transport was assessed. An experimentally derived relationship to predict vapor sorption for a variety of soil types under varying soil moisture conditions was incorporated into the two-dimensional finite-element model, Vocwaste. The revised model was then used to simulate the transport of volatile organics. Vapor-phase partitioning in the model accounted for vapor uptake by sorption onto moist mineral surfaces as well as sorption at the liquid-solid interface and dissolution into soil water. Under dry conditions, vapor-phase sorption of volatile organic pollutants was shown to have a retarding effect on transport of organic vapors. However, for shallow, contaminated soils, volatilization was controlled by vapor diffusion, even under dry conditions where vapor-phase sorption was high. The influence of Henry's law constant and of the aqueous-phase (solid-liquid) partition coefficient for volatile organic pollutants was considered in the simulations. Volatilization of organic vapors was shown to be favored for contaminants with high Henry's law constants and low aqueous-phase partitioning coefficients. Because of the interdependence of these two physical-chemical properties, individual properties of the contaminant should not be considered in isolation in the evaluation of vapor transport.     

Soil remediation: humic acids as natural surfactants in the washings of highly contaminated soils

The remediation of the highly contaminated site around the former chemical plant of ACNA (near Savona) in Northern Italy is a top priority in Italy. The aim of the present work was to contribute in finding innovative and environmental-friendly technology to remediate soils from the ACNA contaminated site. Two soils sampled from the ACNA site (A and B), differing in texture and amount and type of organic contaminants, were subjected to soil washings by comparing the removal efficiency of water, two synthetic surfactants, sodium dodecylsulphate (SDS) and Triton X-100 (TX100), and a solution of a natural surfactant, a humic acid (HA) at its critical micelle concentration (CMC). The extraction of pollutants by sonication and soxhlet was conducted before and after the soil washings. Soil A was richer in polycyclic aromatic hydrocarbons, whereas soil B had a larger content of thiophenes. Sonication resulted more analytically efficient in the fine-textured soil B. The coarse-textured soil A was extracted with a general equal efficiency also by soxhlet. Clean-up by water was unable to exhaustively remove contaminants from the two soils, whereas all the organic surfactants revealed very similar efficiencies (up to 90%) in the removal of the contaminants from the soils. Hence, the use of solutions of natural HAs appears as a better choice for soil washings of highly polluted soils due to their additional capacity to promote microbial activity, in contrast to synthetic surfactants, for a further natural attenuation in washed soils.     

A Reexamination of the Ozone Limiting Approach to Estimating Short-Term NO2 Concentrations

The partition and effective diffusion coefficients of formaldehyde were measured for three materials (conventional gypsum wallboard, “green” gypsum wallboard, and “green” carpet) under three relative humidity (RH) conditions (20%, 50%, and 70% RH). The “green” materials contained recycled materials and were friendly to environment. A dynamic dual-chamber test method was used. Results showed that a higher relative humidity led to a larger effective diffusion coefficient for two kinds of wallboards and carpet. The carpet was also found to be very permeable resulting in an effective diffusion coefficient at the same order of magnitude with the formaldehyde diffusion coefficient in air. The partition coefficient (K _ma) of formaldehyde in conventional wallboard was 1.52 times larger at 50% RH than at 20% RH, whereas it decreased slightly from 50% to 70% RH, presumably due to the combined effects of water solubility of formaldehyde and micro-pore blocking by condensed moisture at the high RH level. The partition coefficient of formaldehyde increased slightly with the increase of relative humidity in “green” wallboard and “green” carpet. At the same relative humidity level, the “green” wallboard had larger partition coefficient and effective diffusion coefficient than the conventional wallboard, presumably due to the micro-pore structure differences between the two materials. The data generated could be used to assess the sorption effects of formaldehyde on building materials and to evaluate its impact on the formaldehyde concentration in buildings.

Implications: Based on the results of this study, the sink effects of these commonly used materials (conventional and “green” gypsum wallboards, “green” carpet) on indoor formaldehyde concentration could be estimated. The effects of relative humidity on the diffusion and partition coefficients of formaldehyde were found to differ for materials and for different humidity levels, indicating the need for further investigation of the mechanisms through which humidity effects take place.     

Stack Sampling of Organic Compounds: Application to the Measurement of Catalytic Incinerator Efficiency

Abstract

Ozone dry deposition fluxes and velocities were measured in 1994 in a semi–arid steppe of central Spain and in a forest in southern France during the period of photochemical activity using the gradient method. Downward fluxes were systematically obtained in both sites, with lower values at nighttime and maximum values during the central period of the day, which showed the important role of stomata in ozone uptake. The range of deposition velocities was –0.005 to 1.160 in the forested site and 0.001 to 1.430 cm s–1 in the semi–arid steppe. The nocturnal deposition velocities observed in the semi–arid steppe were considerably higher than in the forest, with values up to 0.35 cm s–1.

A single layer canopy model was applied and validated at both sites. The model fitted the daily patterns well but underestimated the observed values by 34% in the forest and by 10% in the semi–arid steppe. To improve the accuracy of the model, both soil and internal stomatal resistances, Rsoil and Ri, were estimated using a least square technique. The interdependence of both parameters and the relative humidity, rH, was evaluated through a statistical analysis of the residual between the observed deposition velocity and the aerodynamic, sub–layer, and stomatal resistances. The comparison between the parameter estimates under wet and dry conditions in both sites showed (1) the influence of rH on stomatal parameter and soil resistance, (2) the large contribution of stomatal conductance to ozone uptake during the daytime, and (3) the importance of soil as an additional pathway for ozone exchange, especially in the steppe. Taking into account the parameter estimates, the underestimate of the modeled results was 3% in the forest and 5% in the semi–arid steppe.     

Comparison of seasonal variations of ozone exposure and fluxes in a Mediterranean Holm oak forest between the exceptionally dry 2003 and the following year

Ozone and energy fluxes have been measured using the eddy covariance technique, from June to December 2004 in Castelporziano near Rome (Italy), and compared to similar measurements made in the previous year. The studied ecosystem consisted in a typical Mediterranean Holm oak forest. Stomatal fluxes have been calculated using the resistance analogy and by inverting the Penmann-Monteith equation. Results showed that the average stomatal contribution accounts for 42.6% of the total fluxes. Non-stomatal deposition proved to be enhanced by increasing leaf wetness and air humidity during the autumnal months. From a comparison of the two years, it can be inferred that water supply is the most important limiting factor for ozone uptake and that prolonged droughts alter significantly the stomatal conductance, even 2 months after the soil water content is replenished. Ozone exposure, expressed as AOT40, behaves similarly to the cumulated stomatal flux in dry conditions whereas a different behaviour for the two indices appears in wet autumnal conditions. A difference also occurs between the two years.     

What environmental fate processes have the strongest influence on a completely persistent organic chemical's accumulation in the Arctic?

Fate and transport models can be used to identify and classify chemicals that have the potential to undergo long-range transport and to accumulate in remote environments. For example, the Arctic contamination potential (ACP), calculated with the help of the zonally averaged global transport model Globo-POP, is a numerical indicator of an organic chemical's potential to be transported to polar latitudes and to accumulate in the Arctic ecosystem. It is important to evaluate how robust such model predictions are and in particular to appreciate to what extent they may depend on a specific choice of environmental model input parameters. Here, we employ a recently developed graphical method based on partitioning maps to comprehensively explore the sensitivity of ACP estimates to variations in environmental parameters. Specifically, the changes in the ACP of persistent organic contaminants to changes in each environmental input parameter are plotted as a function of the two-dimensional hypothetical “chemical space” defined by two of the three equilibrium partition coefficients between air, water and octanol. Based on the patterns obtained, this chemical space is then segmented into areas of similar parameter sensitivities and superimposed with areas of high default ACP and elevated environmental bioaccumulation potential within the Arctic. Sea ice cover, latitudinal temperature gradient, and macro-diffusive atmospheric transport coefficients, and to a lesser extent precipitation rate, display the largest influence on ACP-values for persistent organic contaminants, including those that may bioaccumulate within the polar marine ecosystems. These environmental characteristics are expected to be significantly impacted by global climate change processes, highlighting the need to explore more explicitly how climate change may affect the long-range transport and accumulation behavior of persistent organic pollutants.     

Influence of soil moisture on the sequestration of organic compounds in soil

A study was conducted as a part of continuing investigation of the effect of soil moisture on the sequestration of organic compounds aged in the soil. Here, experiments focused on the effects of moisture changes within the soil before, during, and after contaminant addition. The extractability of aged (68 d) phenanthrene was greater from soil that had been subjected to wetting and drying cycles prior to solute addition as compared to soil initially maintained at constant moisture. The recovery of phenanthrene added to moist soil was increased relative to extractability from soil that was air-dried at the time of the contaminant addition. Repeated wetting and drying of soil after the addition of atrazine or phenanthrene resulted in decreased extractability of the compounds as compared to samples maintained at constant moisture. A method for rapidly sequestering contaminants is proposed and may be useful in limiting the time required for laboratory studies involving “aged” contaminants. These data build upon the findings of earlier work from our laboratory and indicate that changes in the moisture conditions of soil can affect the availability of sequestered contaminants possibly through alterations in the structure of the natural solid.     

Interactions of Environmental Factors on the Sensitivity of Plants to Air Pollution

Before potential damage to vegetation can be adequately forecast, even after an air pollution alert has been placed in effect, a clear understanding of the interactions of environment on plant sensitivity must be ascertained. This involves detailed study of single factors and then multiple factors using the phytotoxicants in question. Factors studied or suggested include light (quality, intensity, and duration), temperature, carbon dioxide concentration, humidity, wind, soil moisture, soil aeration, nutrient levels, and soil texture. This paper presents a review of the work relating plant injury to specific air pollutants as conditioned by several environmental conditions supported by research on the interactions of ozone with these environmental conditions.     

Impact of dry deposition of semi-volatile organic compounds on secondary organic aerosols

Dry deposition of semi-volatile organic compounds (SVOC) is not currently treated in most chemical transport models of air quality and this omission has been identified as a possible major source of uncertainty. The effect of dry deposition of SVOC on the concentration of secondary organic aerosols (SOA) is investigated in summertime with the chemical transport model CHIMERE that simulates SOA concentrations by means of molecular SOA surrogate species. Omitting dry deposition could overestimate SOA concentrations by as much as 50%. This overestimation is larger during nighttime due to higher relative humidity.     

Brown rust disease control in winter wheat: I. Exploring an approach for disease progression based on night weather conditions

An empirical approach for simulating the infection and progress of leaf rust (caused by Puccinia triticina) during stem elongation on winter wheat was analysed for the 2000 to 2006 growing seasons. The approach was elaborated based on night weather conditions (i.e., air temperature, relative humidity and rainfall) and leaf rust occurrences. Data from three consecutive cropping seasons (2000–2002) at four representative sites of the Grand-Duchy of Luxembourg were used in the set-up phase. The capability to correctly simulate the occurrence expression of P. triticina infections on the upper leaf layers was then assessed over the 2003–2006 period. Our study revealed that the development of leaf rust required a period of at least 12 consecutive hours with air temperatures ranging between 8 and 16 °C, a relative humidity greater than 60 % (optimal values being 12–16 °C and up to 80 % for air temperatures and relative humidity, respectively) and rainfall less than 1 mm. Moreover, leaf rust occurrences and infections were satisfactorily simulated. The false alarm ratio was ranged from 0.06 to 0.20 in all the study sites. The probability of detection and critical success index for WLR infection were also close to 1 (perfect score).     

A neural network-based approach for the prediction of urban SO2 concentrations in the Istanbul metropolitan area

A three-layer Artificial Neural Network (ANN) model was developed to forecast air pollution levels. The subsequent SO₂ concentration (24-hour averaged) being the output parameter of this study was estimated by seven input parameters such as preceding SO₂ concentrations (24-hour averaged), average daily temperature, sea-level pressure, relative humidity, cloudiness, average daily wind speed and daily dominant wind direction. After Backpropagation training combined with Principal Component Analysis (PCA), the proposed model predicted subsequent SO₂ values based on measured data. ANN testing outputs were proven to be satisfactory with correlation coefficients of about 0.770, 0.744 and 0.751 for the winter, summer and overall data, respectively.     

The interfacial mass transfer resistances of the ozone dry deposition over the field soil of Taichung County in Taiwan

This study aims to design a dry deposition chamber and to measure ozone depletion over the Taichung field soil. This study seeks to verify the phenomena by an experimental and mathematical model. It is demonstrated that interfacial mass transfer resistances of ozone dry deposition involve reactive resistance (R(sr)) and kinetic resistance (R(sk)). It reveals the chemical reaction (O3 + NO --> NO2) to produce the reactive resistance, and verifies that the interfacial mass transfer resistances depend on nitrogen oxide emission and soil temperature. It shows that the interfacial mass transfer resistances are reduced with increasing soil temperature (T(S)). The model profiles are smaller than the observed data within a relative error of 15%. The reactive resistance decreases exponentially with increasing soil temperature; R(sr)(-1) (cm x sec(-1)) = 0.0001 exp (0.1455T(S)). The kinetic resistance decreases linearly with increasing soil temperature; R(sk)(-1)(cm x sec(-1)) = 0.0108T(S) + 1.4012. This model is more accurate with higher soil temperature and larger ozone concentration. Results are consistent with thermodynamics and reaction kinetics. Ozone dry deposition over agricultural soil causes conversion of nitrogen oxide (NO) to nitrogen dioxide (NO2).     

Polycyclic aromatic hydrocarbons in Costa Rican air and soil: A tropical/temperate comparison

Surface soil and passive air samples from a network of 23 sampling sites across Costa Rica were analyzed for polycyclic aromatic hydrocarbons (PAHs), allowing for an evaluation of absolute levels, spatial distribution patterns, air/soil concentration (A/S) ratios and relative composition. Annual mean concentrations of four-ring PAHs in air were low (median of approximately 40 pg m⁻³), except in Costa Rica's densely populated central valley (approximately 650 pg m⁻³). PAH concentrations in soil were also low (median of 5 ng g⁻¹ dry weight) and comparable to those reported for other tropical regions. These low soil concentrations result in A/S ratios of four-ring PAHs in Costa Rica that are higher than the equilibrium air–soil partitioning coefficients and also higher than A/S ratios reported for temperate locations. A series of model calculations of increasing complexity were used to seek an explanation for variable A/S ratios of PAHs under tropical and temperate conditions. Temperature-driven changes in air–soil partitioning and differences in PAH degradability under temperate and tropical conditions are insufficient to explain the higher soil concentrations and lower A/S ratios in temperate regions. However, these can be explained by atmospheric deposition of PAHs during historical periods of much higher emissions and air concentrations and by persistence of PAHs in soils on the order of decades. Low PAH concentrations in tropical soils were found to be consistent with constant or increasing emissions, and in particular, do not require that degradation rates in soil are much faster than in temperate areas. In comparison to temperate soils, soils from Costa Rica and other tropical regions have a higher relative abundance of the lighter PAHs. This likely reflects a higher source contribution from biomass burning in the tropics, as well as the preferential loss of lighter PAHs from temperate soils that experienced high PAH deposition in the past.     

Adsorption of organic vapors on polar surfaces- Recent advances

This paper summarizes recent research on the adsorption of organic vapors on surfaces. Since the low gas phase concentration range is typical for environmental situations, this review is restricted to these adsorption coefficients. Two environmental parameters have a strong influence on the adsorption of organic vapors on polar surfaces:temperature andrelative humidity (which is the most suitable parameter for describing the influence of ambient moisture). An exponential relationship was found for the adsorption coefficientversus relative humidity and the reciprocal temperature, respectively. Comparing the heats of adsorption, two different groups of substances emerged: polar chemicals exhibited heats of sorption which were higher than their corresponding heats of condensation due to their ability to form hydrogen bonds, while for the nonpolar compounds the opposite was true. Sorption takes place on the surface of an adsorbed water film when the relative humidity exceeds the value which is necessary to form a monomolecular layer of water on the surface of the adsorbent (≥ 30 % relative humidity). Therefore, at temperature below 0 °C, a change in the adsorption behavior might be expected due to a change of properties of the adsorbed water film. However, no alterations were observed at temperatures from -12 °C to + 4 °C (adsorption on quartz sand). The results were comparable to those at much higher temperatures (50 – 80 °C). A statistical approach for the prediction of the adsorption coefficients from physico-chemical parameters of the substances (vapor pressure, polarizability, and electron-donating capability) was developed and good agreement was found with experimental results and independent data from the literature. Finally, two special cases, the adsorption on bulk water and ice, are discussed.