Valorization of solid waste products from olive oil industry as potential adsorbents for water pollution control—a review

The global olive oil production for 2010 is estimated to be 2,881,500 metric tons. The European Union countries produce 78.5 % of the total olive oil, which stands for an average production of 2,136,000 tons. The worldwide consumption of olive oil increased of 78 % between 1990 and 2010. The increase in olive oil production implies a proportional increase in olive mill wastes. As a consequence of such increasing trend, olive mills are facing severe environmental problems due to lack of feasible and/or cost-effective solutions to olive-mill waste management. Therefore, immediate attention is required to find a proper way of management to deal with olive mill waste materials in order to minimize environmental pollution and associated health risks. One of the interesting uses of solid wastes generated from olive mills is to convert them as inexpensive adsorbents for water pollution control. In this review paper, an extensive list of adsorbents (prepared by utilizing different types of olive mill solid waste materials) from vast literature has been compiled, and their adsorption capacities for various aquatic pollutants removal are presented. Different physicochemical methods that have been used to convert olive mill solid wastes into efficient adsorbents have also been discussed. Characterization of olive-based adsorbents and adsorption mechanisms of various aquatic pollutants on these developed olive-based adsorbents have also been discussed in detail. Conclusions have been drawn from the literature reviewed, and suggestions for future research are proposed.     

Options for cleanup and disposal of pesticide wastes generated on a small‐scale

Abstract

Many processes have been investigated to dispose of obsolete pesticide stocks and clean up wastewater and contaminated soil. The processes vary in their stages of development and commercial utility. With the exception of incineration, no single process may be amenable to all pesticide waste. Thus, any chosen process must consider first the chemical constituents needing remediation, their concentration, and desired or regulated cleanup objectives. Incineration seems too impractical and expensive to clean up routinely generated wastewater and contaminated soil, but it may currently be the only practical option for obsolete stocks . Practical remediation processes for wastewater and contaminated soil produced by small waste generators are discussed. Cleanup should be viewed as an integration of physical, chemical, and biological technologies.     

Synthesis of an organic–inorganic composite from calcium carbonate and Kraft lignin and its use as carrier material for controlled release of semiochemical agents

Environmental Science and Pollution Research - The control of pests in agricultural systems is currently based on the widespread use of pesticides that efficiently control pests but have negative...     

Sediments as a sink for UV filters and benzotriazoles: the case study of Upper Iguaçu watershed,Curitiba (Brazil)

Ingredients in home and personal care products, including UV filters and benzotriazoles, are high production volume chemicals extensively used in our daily life, despite several studies revealed their potential eco-toxicity and endocrine-disrupting capacity. Due to some features, such as high lipophilicity, low degradability, and persistence of many of these compounds, sediments can be considered a sink for them in the aquatic environment. In the present study, nine organic UV filters and three benzotriazoles were investigated for the first time in sediments from four urban rivers in Brazil. The contaminants were analyzed by liquid chromatography-tandem mass spectrometry (LC-MS/MS). The results revealed that octocrylene (OC), etylhexyl-methoxycinnamate (EHMC), benzophenone-3 (oxybenzone, BP3), and benzotriazole (BZT) were the predominant compounds adsorbed on the sediments, with concentrations ranging from 5.6 to 322.2 ng g⁻¹ dry weight. The results reported in this work constitute the first data on the accumulation of polar benzotriazoles and lipophilic organic UV filters in sediments from Brazil.

     

Henry’s law constant measurements for formaldehyde and benzaldehyde as a function of temperature and water composition

Henry’s law constants H of formaldehyde and benzaldehyde were determined using a dynamic system based on the water/air equilibrium at the interface within the length of a microporous tube. The measurements were conducted over the range 273–293 K in (i) deionized water, (ii) 35 g L^?1 solution of NaCl simulating seawater and (iii) two nitric acid solutions, i.e. 0.63 and 6.3 wt%.In pure water, the obtained data were used to derive the following Arrhenius expressions: ln H = (6423 ± 542)/T ? (13.4 ± 2.0) and ln H = (6258 ± 280)/T ? (17.5 ± 1.0) for formaldehyde and benzaldehyde, respectively. The H values, calculated at 293 K from Arrhenius expressions cited above were the following (in units of M atm^?1): H = 5020 ± 1170 (formaldehyde), H = 47 ± 5 (benzaldehyde). The temperature dependence of H permits then to derive the solvation enthalpies for both compounds: ΔH_solv = ?(53.4 ± 4.5) kJ mol^?1 and ΔH_solv = ?(52.0 ± 2.3) kJ mol^?1 for formaldehyde and benzaldehyde, respectively.In 35 g L^?1 salt solution, the H values were 27–66% and 12–21% lower than their respective determinations in deionized water, for formaldehyde and benzaldehyde respectively. The observed salt effect was used to estimate the following Setschenow coefficients at 293 K for 0.6 M NaCl: formaldehyde (0.21) and benzaldehyde (0.09).In 6.3 wt% nitric acid solution, H values of benzaldehyde were approximately 30% higher than those found in pure water although no significant influence was observed for formaldehyde.Finally, our experimental data were then used to estimate the fractions of formaldehyde and benzaldehyde in atmospheric aqueous phase and their derived atmospheric lifetimes.     

Pollution of water in Africa: a review of contaminants and fish as biomonitors and analytical methodologies—the case of Senegal

Environmental Science and Pollution Research - Environmental pollution is one of the major problems facing human health, ecosystems, and biodiversity. This is particularly the case for water...     

Macroinvertebrate community as a biological indicator of ecological and toxicological factors in Lake Saint-François (Québec)

To assess the potential of the macroinvertebrate community for monitoring variation in the environmental quality of large rivers, the response of littoral macrobenthos in Lake Saint-Fran?ois, a fluvial lake of the St Lawrence River (Québec) are described. First, the composition of total macroinvertebrate communities and important taxonomic groups as well as the biotic ICI-SL index in 16 littoral stations varying in sedimentology, water chemistry and contamination are described to define indicator species groups and environmental quality ranks. Thereafter, the relative contribution of ecological and toxicological factors in explaining the variation observed in macroinvertebrate assemblages and biotic index were quantified using partial canonical correspondence analysis. Cluster analyses based on taxonomic composition separated five groups of stations where macroinvertebrate assemblages varied in density, composition and tolerance to pollution. The ICI-SL biotic index varied from 7.2 to 27.2 with a mean value of 19 +/- 6. The ICI-SL values determined for the macroinvertebrate communities in Lake Saint-Fran?ois did not reflect an important deterioration in environmental quality, and there was some agreement between the environmental quality ranking of the stations expressed either by the ICI-SL index or the community cluster analysis. Water conductivity and phosphorus concentration, followed by macrophyte types (Chara, Ceratophyllum) and sediment grain size, were the most significant ecological variables to explain variation in macroinvertebrate communities and derived ICI-SL index in Lake Saint-Fran?ois. Among the toxicological factors, metals in water (Fe, Cr, Pb, Mn, Zn) and sediment (Mn, Pb, Se), as well as the composite indices of metal and organic contamination (water CI, sediment CI, sediment total PAHs) were the most important factors. The contamination factors selected in our models represented contaminant sorption processes rather than direct toxicological effects. The lack of clear relationships between contaminants and macroinvertebrate variables reflected the relative low level of contamination in the stations sampled in Lake Saint-Fran?ois. There were some interactions between toxicological and ecological variables that should be considered in the planning of sampling and interpretation of biomonitoring studies. However, the large amount of unexplained variance (49.2-86.6%) in the CCA models underlined the limitations of the use of the indices of macroinvertebrate community structure that were assessed in this study for biomonitoring purposes in the absence of a contrasting pollution gradient.     

The use of vegetation,bees, and snails as important tools for the biomonitoring of atmospheric pollution—a review

The continuous discharge of diverse chemical products in the environment is nowadays of great concern to the whole world as some of them persist in the environment leading to serious diseases. Several sampling techniques have been used for the characterization of this chemical pollution, although biomonitoring using natural samplers has recently become the technique of choice in this field due to its efficiency, specificity, and low cost. In fact, several living organisms known as biomonitors could accumulate the well-known persistent environmental pollutants allowing their monitoring in the environment. In this work, a review on environmental biomonitoring is presented. The main sampling techniques used for monitoring environmental pollutants are first reported, followed by an overview on well-known natural species used as passive samplers and known as biomonitors. These species include conifer needles, lichen, mosses, bees and their byproducts, and snails, and were widely used in recent research as reliable monitors for environmental pollution.

     

Iron oxide nanoparticles embedded in organic microparticles from Yerba Mate useful for remediation of textile wastewater through a photo-Fenton treatment: Ilex paraguariensis as a platform of environmental interest – Part 1

Environmental Science and Pollution Research - Seven composites of iron oxide nanoparticles embedded in organic microparticles mediated by Cu(II) were synthesized using yerba mate (Ilex...     

New ternary water-soluble support from self-assembly of β-cyclodextrin-ionic liquid and an anionic polymer for a dialysis device

Environmental Science and Pollution Research - We developed a new hybrid material resulting from an innovative supramolecular tripartite association between an ionic liquid covalently immobilized...     

Allergy from perspective of environmental pollution effects: from an aspect of atopic dermatitis,immune system,and atmospheric hazards—a narrative review of current evidences

Environmental Science and Pollution Research - Environmental pollution has become more diversified in recent years as technologies for urbanization is increasingly more advanced. Several...     

A cheap protocol for colour measure and for diagnostic in planning a cultural heritage restoration. Case study: main façade of Palazzo Governi (Cagliari,Sardinia, Italy)

Due to the bad state of conservation, “Palazzo Governi”, a seventeenth-century building located in the old town district of “Stampace” in Cagliari (Sardinia, Italy), was subjected to restoration. Thus, according to the Italian Law n. 1089, the main façade colour must be reproduced, and therefore, its identification was required. The available samples looked fairly degraded, in particular as an easy plaster to crumble; so, some other analyses able to identify the degradation cause were performed. Two different approaches were adopted to attain the first goal, the visual colour assessment by a sensory panel (subjective) and the instrumental measurement by colorimetry (objective). Ion chromatography and inductively coupled plasma–optical emission spectroscopy analyses, as well as conductivity and pH measurements, were performed to evaluate the presence of water-soluble salts inside the plaster, as possible cause of degradation; the binder/aggregate ratio was also evaluated. A full mineralogical and petrographic characterisation of the materials constituting the samples, as well as the identification of their stratigraphy and some other morphologic and structural features suitable to highlight eventual forms of degradation, were performed by optical microscopy. Scanning electron microscopy coupled to X-ray microanalysis was been also used in order to confirm and/or to integrate data obtained by optical microscopy. The samples have been compared with two samples coming from two other buildings, also located in Sardinia, that looked in good conservation state. The results evidenced that the causes of degradation come from a high salt (especially sulphate) content and a scarce presence of binder in the plaster that can be imputed to a wrong initial composition and/ or to a leaching by acidic rain.     

Vegetational and mycorrhizal successions at a metal polluted site: Indications for the direction of phytostabilisation?

Plant communities on plots with different metal pollution levels were compared in a field study in order to select the most suitable plant species for the direction of secondary succession toward the targeted grassland vegetation. The vegetational succession showed a gradual increase in plant cover and the number of plant species on the less polluted locations. Two predominant grass species Calamagrostis varia and Sesleria caerulea were selected for phytostabilisation, but a severely reduced seed germination capacity obstructed their use in practice. The mycorrhizal succession showed a gradual replacement of non-mycorrhizal with mycorrhizal plant species. Similar levels of arbuscular mycorrhizal colonisation of a particular plant species may be developed within each growing season regardless of the levels of pollution, with the exception of vesicle/intraradical spore formation. The results suggest that lower overall mycorrhizal colonisation levels and increased vesicle/spore formation may be a part of a mycorrhizal strategy at the most polluted locations.     

Light Scattering Characteristics of Aerosols at Ambient and as a Function of Relative Humidity: Part II—A Comparison of Measured Scattering and Aerosol Concentrations Using Statistical Models

ABSTRACT

The eastern United States national parks experience some of the worst visibility conditions in the nation. To study these conditions, 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. It is a cooperative three-year study that is sponsored by the National Park Service and the Electric Power Research Institute and its member utilities. The field portion of the study was carried out from July 15 to August 25, 1995.

The study design, instrumental configuration, and estimation of aerosol types from particle measurements is presented in a companion paper. In the companion paper, we compare measurements of scattering at ambient conditions and as functions of relative humidity to theoretical predictions of scattering. In this paper, we make similar comparisons, but using statistical techniques. Statistically derived specific scattering associated with sulfates suggest that a reasonable estimate of sulfate scattering can be arrived at by assuming nominal dry specific scattering and treating the aerosols as an external mixture with ammoniation of sulfate accounted for and by the use of Tang's growth curves to predict water absorption. However, the regressions suggest that the sulfate scattering may be underestimated by about 10%. Regression coefficients on organics, to within the statistical uncertainty of the model, suggest that a reasonable estimate of organic scattering is about 4.0 m²/g.

A new analysis technique is presented, which does not rely on comparing measured to model estimates of scattering to evoke an understanding of ambient aerosol growth properties, but rather relies on measurements of scattering as a function of relative humidity to develop actual estimates of f(RH) curves. The estimates of the study average f(RH) curve for sulfates compares favorably with the theoretical f(RH) curve for ammonium bisulfate, which is in turn consistent with the study average sulfate am-moniation corresponding to a molar ratio of NH₄/SO₄ of approximately one. The f(RH) curve for organics is not significantly different from one, suggesting that organics are weakly to nonhygroscopic.     

Titanium dioxide and graphitic carbon nitride–based nanocomposites and nanofibres for the degradation of organic pollutants in water: a review

Environmental Science and Pollution Research - The paper reviews graphitic carbon nitride–based nanostructured photocatalytic materials and nanofibres for applications in water purification....     

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

ABSTRACT

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 μm inlet. Fine particle (<2.5 μm) 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.     

Environmental exposure to metals and the risk of high blood pressure: a cross-sectional study from NHANES 2015–2016

Environmental Science and Pollution Research - Exposure to metal pollution can be caused from inhalation, ingestion, or absorption from air, water, or food. Chronic exposure to trace amounts of...     

Carbon dots decorated magnetite nanocomposite obtained using yerba mate useful for remediation of textile wastewater through a photo-Fenton treatment: Ilex paraguariensis as a platform of environmental interest—part 2

Environmental Science and Pollution Research - Two carbon dots (CD) with diameters of 4.9?±?1.5 and 4.1?±?1.2&nbsp;nm were successfully synthesized through an...     

Deposition and regional distribution of HCHs and p,p′-DDX in the western and southern Tibetan Plateau: records from a lake sediment core and the surface soils

Tibetan Plateau is the world’s highest plateau, which provides a unique location for the investigation of global fractionation of organochlorine pesticides (OCPs). In this study, deposition and regional distribution of HCHs and p,p′-DDX in the western and southern Tibetan Plateau were investigated by the records from a sediment core of Lake Zige Tangco and 24 surface soils. Concentration of ΣHCHs in the surface soils of the western Tibetan Plateau was much higher than that of the southern part. Maximum fluxes of α-, β-, and δ-HCH in the sediment core were 9.0, 222, and 21 pg cm^?2 year^?1, respectively, which appeared in the mid-1960s. Significant correlations were observed between concentrations of α- and β-HCH in both the surface soils and the sediment core. Concentrations of both α- and β-HCH increased with the inverse of the average annual temperature of these sites. γ-HCH became the dominant isomer of HCHs after the late 1970s, and reached the maximum flux of 160 pg cm^?2 year^?1 in the early 1990s. There were no significant correlations between concentrations of γ-HCH and the other isomers in both the surface soils and the sediment core. The results suggested that there was input of Lindane at scattered sites in this area. In contrast to ΣHCHs, concentration of Σp,p′-DDX in the surface soils of the southern part was much higher than that of the western part. Maximum flux of Σp,p′-DDX was 44 pg cm^?2 year^?1, which appeared in the mid-1960s. Local emission of p,p′-DDT was found at scattered sites. This study provides novel data and knowledge for the OCPs in the western and southern Tibetan Plateau, which will help understand the global fractionation of OCPs in remote alpine regions.