The disposal of scrap rubber tires has induced critical environmental issue worldwide due to the rapid increase in the number of vehicles. Recycled scrap tires as a construction material in civil engineering have significant environmental benefits from a waste management perspective. A systematic study that deals with strength and microstructure characteristics of the rubber-sand mixtures is initiated, and mechanical response of the mixtures is discussed in this investigation. Experiments were conducted to evaluate the effects of rubber fraction on the basic properties including mass density (ρ), stress-strain characteristics, shear strength, and unconfined compression strength (q ᵤ) of the rubber-sand mixtures. Additionally, scanning electron microscopy (SEM) was carried out to reveal the microstructure characteristics of the mixtures with various rubber fractions. A discussion on the micromechanics of the mixtures also was conducted. This study demonstrates that the ρ, friction angle, and q ᵤ decrease linearly with an increase in rubber fraction, whereas shear strain at peak increases. The stress-strain characteristics of the rubber-sand mixtures shift from brittle to ductile as the rubber fraction increase. These changes are attributed to remarkably lower stiffness and higher compressibility of the rubber particle compared with those of the conventional mineral aggregates. With an increase in the rubber fraction, the mechanical response of rubber-sand mixtures exhibits two types: sand-like material and rubber-like material. Rubber particle possesses the capacity to prevent the contacted sand particles from sliding at lower rubber fraction, whereas it transmits the applied loadings as the rubber fraction increased. This outcome reinforces the practicability of using recycled rubber tire-sand mixtures as a lightweight backfill in subbase/base applications.

The removal of antibiotic sulfamethazine (SMT) and its intermediates from water was investigated using a rotating advanced oxidation contactor (RAOC) equipped with TiO₂-high-silica zeolite composite sheets. SMT was readily removed from water through adsorption onto high-silica zeolite and photocatalytic decomposition by TiO₂ inside the composite sheet. Some degradation intermediates were retained and photocatalytically decomposed inside the composite sheet. Relatively hydrophobic intermediates such as hydroxylated SMT were captured inside the sheets, whereas hydrophilic intermediates were distributed in water. This was attributed to the hydrophobic interactions in the adsorption mechanism of high-silica zeolite. The time courses of the NH₄⁺, NO₃⁻, and SO₄²⁻ ion concentration during the RAOC treatment of SMT were evaluated. After treatment by RAOC for 24 h, approximately 94% of nitrogen derived from the amino and sulfanilamide groups and 39% of sulfur from the sulfanilamide group were mineralized, which indicated that the mineralization behavior of SMT treated by RAOC was different from that treated by TiO₂ powder. These results strongly suggested that the dissociation of the amino group and cleavage of the sulfonamide group and subsequent dissociation of the amino group preferentially proceeded inside the composite sheets.

In November 2013, the total concentration of selected heavy metals in 43 urban dust samples, collected from two small-sized cities of industrial E’zhou and agricultural Huanggang, located in the southeastern Hubei province, central China, was detected quantitatively by flame atomic absorption spectrometric (FAAS) for ultimate purpose of pollution monitoring and risk evaluation. Results indicated that the mean concentrations exceeding their respective background values were observed for all the investigated metals, with the exception of Co (13.08mg kg⁻¹) and Fe (38635.02mg kg⁻¹) in Huanggang road dusts, whose average concentrations were close to the background levels. In comparison with the reference data reported from the selected cities worldwide, the urban road dusts were seriously polluted by heavy metals to diverse degrees. The contour distribution maps implied that obviously higher values zones were found between two different types of urban areas, located to both sides of the coastline of Yangtze River. Multivariate statistical analysis revealed that the enriched heavy metals had emanated from the combined effects of both natural sources and anthropogenic sources. Three pollution indices indicated that the riskiest element mainly comprising Cr, Ni, Cu, and Pb appeared to be the major contributors to the urban environmental pollution. Avoiding continuous damage requires, the riskiest metallic contaminants should be paid preferential attention to.

Characteristics of physicochemical parameters, dissolved-phase heavy metals, and polycyclic aromatic hydrocarbons (PAHs) were investigated for 68 urban snowmelt surface runoff and snowpack samples collected from five different functional areas in Beijing, including a business area (BA), a cultural and educational area (CEA), a garden area (GA), a residential area (RA), and a roadside area (RSA). Both snowmelt surface runoff and snowpack were significantly polluted by organic matter, as indicated by their high concentrations of chemical oxygen demand (COD) and total organic carbon (TOC). Among the 11 heavy metals analyzed, Zn was the most enriched in all samples, followed by Mn, Fe, and Cu, whereas the concentrations of Pb, Cr, Cd, As, Ni, Sb, and Co were comparatively low. The results suggested that typical traffic emissions, natural events, industrial practices, and human activities were mainly sources of heavy metals. Low molecular-weight (LMW) PAHs were the dominant sources in snowmelt and snowpack. Anthracene (Ant) and fluorene (Flo) were the most enriched PAHs in both snowmelt surface runoff and snowpack. Coal burning for heating and traffic activities were the most important contributors of PAH pollutants in snowmelt surface runoff and snowpack in Beijing in the winter. Ecological risk assessment demonstrated, however, that heavy metals in snowmelt surface runoff pose little risk to downstream aquatic environments. A middle potential ecological risk could be caused by Ant, Flo, benzo[g, h, i]perylene (BghiP), and benzo[a]pyrene (BaA).

This paper investigates dynamic variation in the morphologic distribution of dense non-aqueous phase liquids (DNAPLs), which take into account the coupled mass transfer. Experiments were carried out in a 2D tank representing a reconstructed aquifer model. DNAPL dissolution rates were investigated over a wide range of DNAPL saturations, several source configurations, and different hydraulic conditions. Morphometric indexes are presented that take into consideration further factors affecting the dissolution process. Local information regarding transport parameters related to the characteristics of the medium was obtained through a neural network and an optimization algorithm applied to experimental tracer tests. The history of DNAPL source architecture, in terms of saturation, indentation grade, and orientation, was determined by image analysis. Dissolved concentrations were registered and mass transfer rate coefficients were obtained for a wide range of source-zone configurations. A statistical analysis was performed to develop a constitutive equation that is descriptive of the mass transfer rate as a function of source-zone metric characteristics. A new empirical dissolution model using the proposed morphometric parameters is presented and compared with other models. The mass transfer correlation reported incorporates morphometric parameters and considers the complex and variable architecture of non-miscible contaminants. The proposed correlation can be used for an initial assessment of non-aqueous phase liquid (NAPL) dissolution rates over a wide range of saturation (residual and non-residual) conditions and different aqueous phase velocities within the NAPL source zone.

This study aims to investigate the association of urinary concentration of phthalate metabolites with body mass index (BMI) and waist circumference (WC) in 2016 on 242 children and adolescents, aged 6–18 years living in Isfahan, Iran. Urinary concentration of mono-butyl phthalate (MBP), mono-benzyl phthalate (MBzP), mono-2-ethylhexyl phthalate (MEHP), mono-methyl phthalate (MMP), mono (2-ethyl-5-exohexyl) phthalate (MEOHP), and mono (2-ethyl-5hydroxyhexyl) phthalate (MEHHP) metabolites were determined. For comparison of means, t test and to evaluate the association of analytes in different groups according to weight ANOVA was used. The correlation was applied to determine the association between phthalate metabolites with age, sex, WC, BMI, and BMI z-score. The univariate and multivariate regression models were used to determine the association of metabolites concentration with BMI z-score and WC. Mean (SD) BMI, BMI z-score and WC were 23.89 (4.41) kg/m², 1.37 (1.3), and 82.37 (12.71) cm, respectively. There was a significant correlation between boys’ age with BMI z-score (p value = 0.03) and WC (p value = 0.01), while the corresponding figures were not statistically significant in girls (p value = 0.48, and 0.4, respectively). Of the total population, 37 participants (15.3%) were obese. MMP, MBP, and MBzP metabolites were observed in all samples while MEHP, MEOHP, and MEHHP in 99.6, 95.86, and 96.28% of the studied population. Mean concentration of MMP (64.38 μg/L) and MBzP (268 μg/L) had the lowest and highest concentrations of metabolites, respectively. A significant relationship was observed among all studied metabolites and weight groups (p value ≤ 0.02). After adjustment for potential confounders, all metabolites (except MMP) showed a low-to-moderate positive and significant relationship with BMI z-score (β = 0.17–0.3). A weak to moderate positive and significant relationship was observed between all phthalate metabolites and WC (β = 0.14–0.39). The concentration of phthalate metabolites was much higher in the population living in Isfahan-Iran than in some other populations, indicating a high exposure to contaminants. Therefore, further studies and preventive measures are required for improving the environmental health.

Anaerobic co-digestion of sewage sludge and glycerol from the biodiesel industry was evaluated in three experimental stages. In the first step, the addition of higher proportions of crude glycerol (5–20% v/v) to the sludge was evaluated, and the results showed a marked decrease in pH and inhibition of methane production. In the second step, co-digestion of sludge with either a lower proportion (1% v/v) of crude glycerol or glycerol pretreated to remove salinity resulted in volatile acid accumulation and low methane production. The accumulation of volatile acids due to the rapid degradation of glycerol in the mixture was more detrimental to methanogenesis than the salinity of the crude glycerol. In the third step, much lower amounts of crude glycerol were added to the sludge (0.3, 0.5, 0.7% v/v), resulting in buffering of the reaction medium and higher methane production than in the control (pure sludge). The best condition for co-digestion was with the addition of 0.5% (v/v) crude glycerol to the sewage sludge, which equals 0.6 g glycerol/g volatile solids applied. Under this condition, the specific methane production (mL CH₄/g volatile solids applied) was 1.7 times higher than in the control.

Cement solidification is an important pre-treatment technology for municipal solid waste incineration (MSWI) fly ash into landfill. The physicochemical properties and leaching characteristics are the foundation for assessing the long-term stability of the fly ash solidified with benchmark cement in landfills. The leaching performances of bulk components (Na, K, Ca, Cl, CO₃²⁻, and SO₄²⁻) and heavy metals (Cu, Zn, Cr, Pb, and Zn) were analyzed based on the percolation column test and pH dependent test respectively. The research showed that in the cement-solidified fly ash, Na and K were mainly in the form of soluble chloride salts and would be washed out severely at the initial leaching stage due to the weak fixation effect of cement. Moreover, a considerable amount of Ca was washed out simultaneously with Na and K, causing a temporary increase in pH value, and then Ca leaching was controlled by the solubility of minerals, mainly calcium carbonate, ettringite formed with CO₃²⁻ and SO₄²⁻. Cement solidification reduced the cumulative release of mobile Cu, Zn, Cr, Pb, and Cd contained in MSWI fly ash. In the cement-solidified fly ash, the leaching of Cu and Zn was controlled by mineral solubility under alkaline conditions, Cr was dependent on the redox conditions, and Pb was related to the complex structures formed with Si–O bonds of silicates. A further research on the long-term stability of the cement-solidified fly ash in landfills was needed.

The presence and accumulation of plastic and microplastic (MP) debris in the natural environment is of increasing concern and has become the focus of attention for many researchers. Plastic debris is a prolific, long-lived pollutant that is highly resistant to environmental degradation, readily adheres hydrophobic persistent organic pollutants and is linked to morbidity and mortality in numerous aquatic organisms. The prevalence of MPs within the natural environment is a symptom of continuous and rapid growth in synthetic plastic production and mismanagement of plastic waste. Many terrestrial and marine-based processes, including domestic and industrial drainage, maritime activities agricultural runoff and wastewater treatment plants (WWTPs) effluent, contribute to MP pollution in aquatic environments. MPs have been identified in food consumed by human and in air samples, and exposure to MPs via ingestion or inhalation could lead to adverse human health effects. Regulations in many countries have already been established or will soon be implemented to reduce MPs in aquatic environments. This review focuses on the occurrence, sources, and transport of MPs in terrestrial and aquatic environments to highlight potential human health effects, and applicable regulations to mitigate impacts of MPs. This study also highlights the importance of personality traits and cognitive ability in reducing the entry of MPs into the environment.

Chemical composition and antifungal activity of essential oils of Algerian Mentha species were studied. Chemical compositions of different Mentha species oils (Mentha rotundifolia, M. spicata, M. pulegium, and M. piperita) were investigated by capillary GC and GC/MS, and their antifungal activities were evaluated by means of paper disc diffusion method and minimum inhibitory concentration (MIC) assays. In total, 98 components from all Mentha species were identified. All oils were rich in monoterpene-oxygenated components. In addition, we reported fumigant antifungal activity of Algerian Mentha essential oils against four fungi: Botrytis cinerea, Penicillium expansum, Monilinia laxa, and M. fructigena. All oils demonstrated very good inhibition especially against B. cinerea, M. laxa, and M. fructigena. Both Monilinia fungi were extremely sensitive to all Algerian Mentha oils, which suggests that Mentha essential oils have the potential to be used as bio-pesticides to protect fruit trees, such as apple and pear trees, and provides an alternative to chemical pesticides.