Showing papers in "Water Air and Soil Pollution in 2017"

Chromium in Agricultural Soils and Crops: A Review

Abstract: The mobility and distribution of metals in the environment is related not only to their concentration but also to their availability in the environment. Most chromium (Cr) exists in oxidation states ranging from 0 to VI in soils but the most stable and common forms are Cr(0), Cr(III), and Cr(VI) species. Chromium can have positive and negative effects on health, according to the dose, exposure time, and its oxidation state. The last is highly soluble; mobile; and toxic to humans, animals, and plants. On the contrary, Cr(III) has relatively low toxicity and mobility and it is one of the micronutrients needed by humans. In addition, Cr(III) can be absorbed on the surface of clay minerals in precipitates or complexes. Thus, the approaches converting Cr(VI) to Cr(III) in soils and waters have received considerable attention. The Cr(III) compounds are sparingly soluble in water and may be found in water bodies as soluble Cr(III) complexes, while the Cr(VI) compounds are readily soluble in water. Chromium is absorbed by plants through carriers of essential ions such as sulfate. Chromium uptake, accumulation, and translocation, depend on its speciation. Chromium shortage can cause cardiac problems, metabolic dysfunctions, and diabetes. Symptoms of Cr toxicity in plants comprise decrease of germination, reduction of growth, inhibition of enzymatic activities, impairment of photosynthesis and oxidative imbalances. This review provides an overview of the chemical characteristics of Cr, its behavior in the environment, the relationships with plants and aspects of the use of fertilizers.

The First Evaluation of Microplastics in Sediments from the Complex Lagoon-Channel of Bizerte (Northern Tunisia)

Abstract: Microplastics (MPs) in sediments from the complex lagoon-channel of Bizerte were investigated, for the first time, to evaluate the occurrence and abundance of MPs in Tunisia. After density separation in saline solution, MPs were counted by a stereomicroscope. The number of MPs was at the range of 3–18 items/g sediment (3000–18,000 items/kg dry sediment) and the most contaminated site was of Menzel Abderrahmane (MA) followed by Carrier Bay (CB), Menzel Jemil (MJ) and Channel of Bizerte (C). The MPs gathered during the survey varied in size from 0.3 to 5 mm, and appear in a variety of shapes and colours. The dominant shape was fibre (88.88% in MA, 91.00% in CB, 82.35% in C and 21.05% in MJ). The rest of MPs are fragments whilst no micro beads were found. Colours are clear, white, blue, green, red and black. Cities discharges, fishing activity and industrial production sites are the most likely sources of MPs. This first work provides original data on the presence of MPs that determines their bioavailability to organisms as seafood, and then possibly transfers of to human. The high MP concentrations registered in the complex lagoon-channel of Bizerte suggest that this site is a hotspot for MP pollution and there is an urgency to understand their origins and effects on marine life. The results will provide useful background information for further investigations.

Application of Zeolites for Sustainable Agriculture: a Review on Water and Nutrient Retention

Abstract: Developing urbanization, water shortage, watercourse pollution, and demands for more food due to population growth require a more efficient water irrigation and fertilizer application. Retaining nutrients and water in agricultural soils brings about higher crop yields and prevents pollution of water courses. Among different solutions, zeolites, which are environmental friendly, ubiquitous, and inexpensive, have been extensively employed in agricultural activities. These minerals are considered as soil conditioners to improve soil physical and chemical properties including infiltration rate, saturated hydraulic conductivity (K s), water holding capacity (WHC), and cation exchange capacity (CEC). Natural and surface-modified zeolites can efficiently hold water and nutrients including ammonium (NH4 +), nitrate (NO3 −) and phosphate (PO4 3−), potassium (K+), and sulfate (SO4 2−) in their unique porous structures. Their application as slow-release fertilizers (SRFs) are reported as well. Therefore, zeolite application can improve both water use efficiency (WUE) and nutrient use efficiency (NUE) in agricultural activities and consequently can reduce the potential of surface and groundwater pollution. This review paper summarizes findings in the literature about the impact of zeolite applications on water and nutrient retention in the agriculture. Furthermore, it explores benefits and drawbacks of zeolite applications in this regard.

Alteration in growth, leaf gas exchange, and photosynthetic pigments of maize plants under combined cadmium and arsenic stress

Abstract: Increasing soil contamination by heavy metals is a major threat to environmental safety and global food security. The present study examined the influence of Cd and As stresses on morpho-physiological growth and yield of two contrasting maize cultivars (Run Nong 35 and Dong Dan 80). The Cd (100 μM) and As (200 μM) were applied individually as well as in combination (Cd + As) at 30 DAS. A control without Cd or As stress was also maintained for comparison. Application of Cd and As alone or in combination substantially reduced the growth (plant height, number of leaves per plant, leaf area, stem diameter, and shoot fresh and dry weight) and yield (number of ears per plant, number of kernels per ear, and 100-kernel weight) contributing traits in both maize cultivars particularly in Run Nong 35. Furthermore, pronounced reductions in gas exchange attributes (photosynthesis, stomatal conductance, transpiration rate, and intercellular CO2) and chlorophyll contents were observed in metal-stressed plants. The combined application of Cd and As was more detrimental for maize, and this treatment recorded the maximum reductions in morpho-physiological growth and yield of both cultivars. Cultivar variations were also apparent, and Dong Dan 80 performed better than Run Nong 35 for all the studied attributes. The higher tolerance of Dong Dan 80 was associated with better leaf gas exchange and maintenance of chlorophyll contents in this cultivar under Cd and As stress.

Water Scarcity and Wastewater Reuse Standards in Southern Europe: Focus on Agriculture

Abstract: Climate change affects water resources worldwide, and Southern Europe is one of the areas where water scarcity is expected to increase in the future. Different water scarcity indicators discussed in this manuscript (e.g. total annual actual renewable water resources, water exploitation index and dependency ratio) showed that some parts of this region are already facing water stress and that climate change could have a great impact on their water supply sector. As agriculture is the biggest consumer of water in the world and also in this particular region, potential water scarcity will impose the need to find new water sources. Treated wastewater reuse would decrease the pressure on the environment and is especially suitable for reuse in agriculture since it already contains some nutrients required for plant growth. However, in order to use it safely, treated wastewater must reach a certain quality that should be regulated. In the south of Europe, 4 countries out of 15 have already adopted wastewater reuse regulations (Greece, Italy, Portugal and Spain). This review compares these regulations and discusses their differences.

Removal of Ammonia from Aqueous Solutions, Ground Water, and Wastewater Using Mechanically Activated Clinoptilolite and Synthetic Zeolite-A: Kinetic and Equilibrium Studies

Abstract: Natural zeolite clinoptilolite and synthetic zeolite Na-A were characterized using XRD and SEM to be used as adsorbents for ammonia from aqueous solutions, ground water, and sewage water. Clinoptilolite was mechanically activated for 2, 4, 6, and 8 h to study the effect of activation in enhancing the adsorption capacity. The adsorption by activated natural zeolite and synthetic zeolite is high pH dependent and achieve the best values at pH = 7. The adsorption capacity of activated natural zeolite increases with increasing the activation from 2 to 8 h achieving removal percentage close to that obtained using synthetic zeolite. The equilibrium was obtained after 60 min for synthetic zeolite and all the activated natural zeolite (except 2-h-activated product, the equilibrium was achieved after 30 min). The kinetic studies reflected the high fitness of the adsorption results of activated natural zeolite products and synthetic zeolite with pseudo-second-order model rather than the other kinetic models. The obtained isotherms reflected the formation of S-type isotherm curve for the adsorption using mechanically activated clinoptilolite and L-type curve for the uptake using synthetic zeolite. The results represented well with Langmuir model followed by Temkin and Freundlich model for adsorption using synthetic zeolite. The uptake using mechanically activated clinoptilolite can be represented by Temkin model rather than both Langmuir and Freundlich models. Thermodynamic parameters indicate spontaneous endothermic adsorption of ammonia using all the zeolitic products under investigation. Finally, the mechanically activated natural zeolite and synthetic zeolite exhibit high efficiency in the removal of ammonia and other water pollutants from ground water and sewage water.

Readily Wash-Off Road Dust and Associated Heavy Metals on Motorways

Abstract: Road dust contains a wide range of potentially health-hazardous pollutant sources. In this study, road dust samples were collected from nine locations along the Sydney orbital motorway during wet weather events and analysed for their mineralogy and heavy metal contents. The aim of this study was to examine for the specific particle size fractions in road dust samples that can be associated with anthropogenic pollutant sources, mainly on the prevalence of heavy metals. Surface morphological and elemental composition of the road dust particles was analysed using scanning electron microscopy coupled with energy dispersive X-ray spectroscopy (SEM-EDX). The heavy metal contents and degree of contamination were also investigated including in the two specific particle size fractions of <75 and 75–150 μm. It was found that the particle size fraction of <75 μm made up between 6 and 16% of the entire particle size distributions and contributed to more than 90% of the heavy metal contents. In addition, a moderate to high degree of heavy metal contamination was measured in the collected road dust samples, and this was correlated well with the local traffic volumes. The good correlation between heavy metals and traffic volumes in the finer road dust particle size fraction of <75 μm indicated that the finer road dust particles were not only important in terms of heavy metal attachment, accumulation and mobilisation during wet weather events but they could also provide evidence of potential anthropogenic pollution sources. These findings will facilitate our scientific understanding on the specific role and importance of particle size fractions on the mobilisation of pollutant sources, particularly heavy metals during wet weather events. It is anticipated that this study will assist in the development of best management practices for pollution prevention and control strategies on the frequency of road sweeping and retention pond design to trap fine road dust particles.

Conventional as well as Emerging Arsenic Removal Technologies—a Critical Review

Abstract: Arsenic poisoning from contaminated drinking water has evolved as one of the major health hazards in recent times. High concentrations of arsenic in water and soil have been found in many parts of the world. Developing countries like Taiwan, Chile, Argentina, Bangladesh, Nepal and Vietnam are most affected by the contamination of groundwater with arsenic. These countries also cannot afford expensive and large-scale treatments to remove arsenic from drinking waters to acceptable limits (10 ppb, as recommended by WHO and US EPA). The aim of this review is to summarize low-cost, effective conventional technologies currently described in the literature for arsenic removal that can be used in the third world and developing countries, compare them with the emerging technologies and discuss their advantages and disadvantages along with a brief analysis of arsenic chemistry.

Reaction Mechanism and Degradation Pathway of Rhodamine 6G by Photocatalytic Treatment

Abstract: The photocatalytic degradation of a cationic dye, rhodamine 6G (Rh-6G) under UV light irradiation was carried out. Rh-6G was completely decolorized in 180 min of photo-oxidative degradation period. The extent of degradation was confirmed performing total organic carbon (TOC) analysis, and up to 90.14%, TOC removal was achieved. Several critical analytical techniques including UV-Vis spectroscopy, high-performance liquid chromatography (HPLC), and ultra-performance liquid chromatography coupled with electrospray ionization mass spectrometry (UPLC/MS) were employed to scrutinize the mechanistic insights of the dye photodegradation. The degraded N-demethylation intermediates and several small molecular products were qualitatively identified, and a tentative photodegradation pathway was proposed. Toxicological evaluation of the degradation products was carried out three types of cell lines (MTT assay) and Triticum sativum seeds. In conclusion, enhanced biodegradability accompanied by toxicity reduction confirmed the promising efficiency of photocatalysis for Rh-6G degradation and therefore could be used for the remediation of textile effluents.

Air Contamination by Mercury, Emissions and Transformations-a Review.

Abstract: The present and future air contamination by mercury is and will continue to be a serious risk for human health. This publication presents a review of the literature dealing with the issues related to air contamination by mercury and its transformations as well as its natural and anthropogenic emissions. The assessment of mercury emissions into the air poses serious methodological problems. It is particularly difficult to distinguish between natural and anthropogenic emissions and re-emissions from lands and oceans, including past emissions. At present, the largest emission sources include fuel combustion, mainly that of coal, and “artisanal and small-scale gold mining” (ASGM). The distinctly highest emissions can be found in South and South-East Asia, accounting for 45% of the global emissions. The emissions of natural origin and re-emissions are estimated at 45–66% of the global emissions, with the largest part of emissions originating in the oceans. Forecasts on the future emission levels are not unambiguous; however, most forecasts do not provide for reductions in emissions. Ninety-five percent of mercury occurring in the air is Hg0—GEM, and its residence time in the air is estimated at 6 to 18 months. The residence times of its HgII—GOM and that in Hgp—TPM are estimated at hours and days. The highest mercury concentrations in the air can be found in the areas of mercury mines and those of ASGM. Since 1980 when it reached its maximum, the global background mercury concentration in the air has remained at a relatively constant level.

Activated Biochar Prepared by Pomelo Peel Using H3PO4 for the Adsorption of Hexavalent Chromium: Performance and Mechanism

Abstract: Adsorption of hexavalent chromium (Cr(VI)) using pomelo peel activated biochar (PPAB) as a adsorbent was investigated. The characterization of the adsorbent was studied by Brunauer-Emmett-Teller (BET), thermogravimetric analysis (TGA), X-ray diffraction (XRD), and zeta potentials analysis. The results showed that the PPAB had a high microporous structure and the existence of organic compounds such as hemicellulose, cellulose, and lignin. Various parameters including initial Cr(VI) concentration, pH, and adsorbent dosage were studied. The results indicated that the adsorption process was pH dependent and maximum adsorption capacity of Cr(VI) was 57.637 mg/g at pH 2.0 and 35 °C with PPAB dosage of 0.05 g. The adsorption kinetics fitted well to the pseudo-second-order model and the correlation coefficients were greater than 0.999. The adsorption isotherm data could be better described with the Langmuir model, suggesting the homogeneous and monolayer adsorption. Moreover, the scanning electron microscopy (SEM), energy dispersive spectrometry (EDS), and Fourier transform infrared spectrum (FTIR) results showed that the surface of PPAB had plenty of developed pores after activation and the modification process was deemed to proceed between the O–H groups from pomelo peel and H3PO4 molecules. The main adsorption mechanism was attributed electrostatic interaction and ion exchange between the surface of PPAB and Cr(VI).

Non-thermal plasma as an innovative option for the abatement of volatile organic compounds: A review

Abstract: Volatile organic compounds (VOCs) cause global and local impacts, resulting in environmental, health, and economic adverse effects Industrial and waste management activities are the main anthropogenic stationary sources of VOCs in the atmosphere The traditional technologies for the treatment of VOC-contaminated air present several limitations when treating effluents with low VOC concentrations, high airflow rate, and with compounds with low solubility in water However, a novel technology, based on non-thermal plasmas (NTPs) and catalysis, has shown promising results in air purification In this framework, after an initial overview on NTP-catalysis principles, this review presents and discusses 20 recent papers, with a threefold purpose: evaluating the most recent applications of NTP and NTP-catalysis reactors to the treatment of air-VOC mixtures, analyzing all the parameters that may influence the abatement efficiency and the by-product formation, and providing the reader with insights into the choice of the preferable configurations to use, based on the effluent type and the destination of the treated air As a result of this review, NTPs may represent a promising option for indoor air treatment, especially because of the lower expected byproduct formation when treating low-concentrated VOC mixtures with relatively low air flow rates If the target is the abatement of higher VOC concentrations, the higher energy efficiency obtainable in such conditions makes NTP-catalysis a cost-effective option for industrial applications In addition, the formation of simpler and more soluble by-products makes NTPs a suitable technology for air pretreatment upstream of water-based removal technologies, such as absorption columns and biofilters

Removal of Dyes Using Graphene-Based Composites: a Review

Abstract: Water contamination has reached an alarming state due to industrialization and urbanization and has become a worldwide issue. Dyes contaminate water and are addressed extensively by researchers. Various technologies and materials have been developed for the treatment of contaminated water. Among them, adsorption has attracted great attention due to its ease and cost-effective nature. In recent years, graphene-based composites have shown great potential for the removal of contaminants from water. The literature reveals the usefulness of composites of graphene with metal oxides, carbon derivatives, metal hybrids and polymers for the removal of organic dyes from contaminated water. In this review, efforts have been made to compile the studies on the removal of cationic and anionic dyes from water using graphene-based composites.

Post-catastrophe Analysis of the Fundão Tailings Dam Failure in the Doce River System, Southeast Brazil: Potentially Toxic Elements in Affected Soils

Abstract: On November 5, 2015, after the collapse of the Fundao tailings dam, a massive amount of iron mine waste was released into the Doce River system in southeast Brazil. The aim of our study was to determine the mass fractions of potentially toxic elements in soil affected by the deposition of material by the waste wave. A preliminary screening was performed with portable X-ray fluorescence spectrometry (PXRF) and principal component analysis (PCA). The EPA 3050B method was further applied to digest the samples for quantitative determination of As, Ba, Cr, Cu, Mn, Ni, Pb, V, and Zn by inductively coupled plasma mass spectrometry. PCA was useful to classify the mine waste samples based on the Fe signal from the PXRF spectra, in spite of the heterogeneous nature of the material discharged into the Doce River system. The anomalous levels of As (up to 164 mg kg−1) and Mn (as high as 2410 mg kg−1) found in some mine waste and affected soil samples are within the background ranges typically observed in the soils of the Iron Quadrangle region. The toxicity characteristic leaching procedure shows no evidence of hazards regarding As, but a high natural background level of Mn was found in the mobile fraction. This preliminary environmental assessment highlights the importance of evaluation of long-term effects on soil directly impacted, as well as on the aquatic biota of the Doce River system and adjacent coastal environment given the large affected area, which includes regions with varying background levels of toxic elements.

Methylene Blue Adsorption on Chitosan-g-Poly(Acrylic Acid)/Rice Husk Ash Superabsorbent Composite: Kinetics, Equilibrium, and Thermodynamics

Abstract: A set of chitosan-g-poly(acrylic acid)/rice husk ash hydrogel composites was successfully employed as methylene blue (MB) adsorbent. Maximum MB adsorption capacity of 1952 mg/g of dried hydrogel was obtained with the composite at 5 wt% of rice husk ash (RHA) at pH ≥ 5. The adsorption capacity varied from 1450 to 1950 mg/g with increasing the initial MB concentration from 1500 to 2500 mg/L. The MB removal efficiency was higher than 90% for all samples. At pH ≥ 5, negatively charged groups (–COO−) in the adsorbent were generated, which could strongly interact with the positive charges from MB, favoring adsorption. Adsorption kinetics followed the pseudo-second-order model, which is based on the chemisorption phenomenon, reaching saturation as fast as 1 h of experiments due to the formation of an adsorbed MB monolayer, as suggested by the Langmuir isotherm model (type I). Desorption experiments showed that 75% of loaded MB can be removed from the adsorbent by immersing it in a pH 1 solution. CHT-g-PAAc/RHA5% composite was submitted to five cycles of adsorption/desorption, maintaining its MB removal efficiency at 91%. Therefore, chitosan-g-poly(acrylic acid)/RHA hydrogel composites present outstanding capacity to be employed in the remediation of MB-contaminated wastewaters.

Artificial Neural Network (ANN) for Modelling Adsorption of Lead (Pb (II)) from Aqueous Solution

Abstract: This study investigated the efficiency of rice husk carbon (RHC) for lead (Pb (II)) adsorption. The developed RHC was characterized by CHNS analyser, FTIR and FESEM. BET surface area, micropore area, micropore volume and average pore diameter of RHC were 58.54 m2/g, 14.53 m2/g, 0.007209 mL/g, and 45.46 A, respectively. Batch adsorption experiments were conducted to assess the effect of initial pH, contact time, initial Pb (II) concentration and RHC dose on Pb (II) removal. A contact time of 120 min and a pH value of 5 were found as optimum for Pb (II) adsorption; maximum adsorption occurred at 8 g/L of RHC dose. Artificial neural network (ANN) was applied to model Pb (II) adsorption. For prediction of Pb (II) adsorption from aqueous solution by RHC, the smallest mean square error (MSE) and the largest coefficient of determination (R2) values were, respectively, obtained as 6.0053 and 0.988567 with Levenberg–Marquardt algorithm (LMA). Hence, it was selected as the best training algorithm. Traincgf and traincgp functions followed this function with a MSE of 6.1496 and 6.2967, respectively. Adsorption of Pb (II) by RHC followed pseudo-second-order kinetics. The experimental data were described well by both Langmuir and Freundlich isotherm models. Thermodynamics study revealed that Pb (II) adsorption by RHC was spontaneous and endothermic, and the system randomness increased during the whole process. Pb (II) adsorption capacity of RHC was compared with different adsorbents. As evidenced by its high adsorption capacity, RHC can be used as an effective adsorbent for Pb (II) removal from aqueous solutions and wastewaters.

Water Use and Treatment in Container-Grown Specialty Crop Production: A Review

Abstract: While governments and individuals strive to maintain the availability of high-quality water resources, many factors can "change the landscape" of water availability and quality, including drought, climate change, saltwater intrusion, aquifer depletion, population increases, and policy changes. Specialty crop producers, including nursery and greenhouse container operations, rely heavily on available high-quality water from surface and groundwater sources for crop production. Ideally, these growers should focus on increasing water application efficiency through proper construction and maintenance of irrigation systems, and timing of irrigation to minimize water and sediment runoff, which serve as the transport mechanism for agrichemical inputs and pathogens. Rainfall and irrigation runoff from specialty crop operations can contribute to impairment of groundwater and surface water resources both on-farm and into the surrounding environment. This review focuses on multiple facets of water use, reuse, and runoff in nursery and greenhouse production including current and future regulations, typical water contaminants in production runoff and available remediation technologies, and minimizing water loss and runoff (both on-site and off-site). Water filtration and treatment for the removal of sediment, pathogens, and agrichemicals are discussed, highlighting not only existing understanding but also knowledge gaps. Container-grown crop producers can either adopt research-based best management practices proactively to minimize the economic and environmental risk of limited access to high-quality water, be required to change by external factors such as regulations and fines, or adapt production practices over time as a result of changing climate conditions.

Adsorption of Toxic Metals on Modified Polyacrylonitrile Nanofibres: A Review

Abstract: Removal of toxic metals from aqueous solutions is of high priority in environmental chemistry. Most of the available techniques for this task are considered expensive; however, the adsorption process has been considered the easiest and the cheapest way of removing toxic metals from aqueous solution. The performance of adsorption setup largely depends on the characteristic of adsorbents. One of these characteristic is availability of large surface area. The more the available sites for chelation, the more the amount of metals removed. Therefore, the production of materials of nanoscale is expedient for adsorption purposes. Electrospinning process is one of the technologies that have been employed to produce polyacrylonitrile nanofibres (PAN-nfs). Moreover, PAN-nfs surfaces have also been chemically modified so as to introduce chelating groups such as amine, carboxyl, imines, etc. Here we review PAN-nfs as metal ion adsorbent. With characteristics such as high surface area as well as good mechanical strength, modified PAN-nfs are considered good adsorbents and have been used to remove toxic metals such as cadmium, lead, chromium, mercury, uranium, silver and copper in different ion states from their aqueous solutions. The ease of immobilization of metal-specific ligands on PAN-nfs has been of great interest in selective extraction of metal ions from their aqueous solutions. Also, toxic metals adsorbed on modified PAN-nfs can be recovered through desorption process using acids or bases of various concentrations.

Removal of Phenolic Compounds from Aqueous Solutions Using Sludge-Based Activated Carbons Prepared by Conventional Heating and Microwave-Assisted Pyrolysis

Abstract: Sludge-derived activated carbons (ACs) were prepared by conventional heating and microwave pyrolysis. The ACs were characterized using several analytical and functional techniques and used for removal of six phenolic compounds from aqueous solutions. The adsorbents exhibited similar features and possessed hydrophobic surfaces. The ACs were assigned mesoporous materials, with specific surface areas of up to 641 and 540 m2 g−1 for CAC-500 and MAC-980, respectively. The preliminary results indicated that phenol removal onto the ACs increased in the order: m-cresol < phenol < o-cresol < 2-chrorophenol < 2-nitrophenol < hydroquinone. Hydroquinone exhibited the highest adsorption capacity and was chosen to continue the remaining part of the experimental work—kinetic and isothermal studies. The adsorption kinetic and isotherm data were well described by the Avrami fractionary order and Redlich–Peterson models, respectively. The maximum amounts (Q max) of hydroquinone adsorbed at 25 °C were too high, reaching 1218.3 and 1202.1 mg g−1 for CAC-500 and MAC-980, respectively. The mechanism of adsorption was proposed in this work, and it was suggested that donor–acceptor complex and π–π interactions play major roles in the adsorption process. The adsorbents were also tested on simulated effluents. The two ACs displayed good efficiency for the treatment of industrial simulated effluents.

Sorption of Sulfadiazine, Norfloxacin, Metronidazole, and Tetracycline by Granular Activated Carbon: Kinetics, Mechanisms, and Isotherms

Abstract: Activated carbon has widespread application in antibiotic-loaded wastewater treatment in recent years, owing to its developed pore structure, high superficies reactivity, and excellent mechanical and chemical stability. In this work, sorption experiments of four representative antibiotics, including sulfadiazine (SDZ), norfloxacin (NOR), metronidazole (MDE), and tetracycline (TC), over granular activated carbon (GAC), which was made from maize straw, were firstly studied. Kinetics, mechanism, and isotherm models related to the sorption process were employed. Results revealed that the sorption capacity by GAC followed the order SDZ > NOR > MDE > TC. The sorption kinetics of the four antibiotics well conformed to the pseudo-second-order model. Both the Weber-Morris intraparticle diffusion and Boyd kinetic models conveyed the information that film diffusion was dominant in the sorption process. The sorption isotherm was better fitted to the Langmuir model. This research may pave a basic way for removing antibiotics in municipal and industrial wastewater by activated carbon.

Phytoremediation Potential of Vetiver Grass ( Vetiveria zizanioides ) for Treatment of Metal-Contaminated Water

Abstract: Phytoremediation using vetiver grass (Vetiveria zizanioides) has been regarded as an effective technique for removing contaminants in polluted water. This study was conducted to assess the removal efficiency of heavy metals (Cu, Fe, Mn, Pb, Zn) using vetiver grass (VG) at different root lengths and densities and to determine metals uptake rate by plant parts (root and shoot) between treatments (low and high concentration). Removal efficiency for heavy metals in water by VG is ranked in the order of Fe>Pb>Cu>Mn>Zn. Results showed that VG was effective in removing all the heavy metals, but removals greatly depend on root length, plant density and metal concentration. Longer root length and higher density showed greater removals of heavy metals due to increased surface area for metal absorption by plant roots. Results also demonstrated significant difference of heavy metals uptake in plant parts at different concentrations indicating that root has high tolerance towards elevated concentration of heavy metals. However, the effects were less significant in plant shoot suggesting that metals uptake were generally higher in root than in shoot. The findings have shown potential of VG in phytoremediation for heavy metals removal in water thus providing significant implication for treatment of metal-contaminated water.

How Uncontrolled Urban Expansion Increases the Contamination of the Titicaca Lake Basin (El Alto, La Paz, Bolivia)

Abstract: Cities in developing countries encounter rapid waves of social transformation and economic development where the environment is mostly a neglected aspect. The Katari watershed encompasses mining areas, El Alto city (one of the fastest growing urban areas in South America and the biggest in the Altiplano) as well as agricultural areas. Its outlet is Cohana Bay, one of the most polluted areas of Lake Titicaca. Here we propose an integrative approach (hydrological, physicochemical, chemical and bacterial data) to understand the pollution problem of this developing area, in which a variety of anthropogenic activities takes place. Both mining and urban areas appear to be sources of metal pollution. Nutrient and bacterial contaminations are mainly related to urban and industrial discharges. These situations have impacts in the basin from the mining area down to Cohana Bay of Lake Titicaca. Pollutant concentration patterns are highly influenced by seasonal hydrology variations. The poor quality of surface waters in the basin represents a risk for human and animal populations, as well as for the quality of aquifers located underneath El Alto city.

Highly Efficient Removal of Dye from Water Using Magnetic Carrageenan/Silica Hybrid Nano-adsorbents

Abstract: The discharge of effluents containing organic dyes extensively used in the industry is a matter of concern because these pollutants can cause harmful effects in the environment and human health. In this work, magnetic iron oxide nanoparticles coated with κ-carrageenan/silica organic/inorganic hybrid shells were synthesized and used as novel adsorbents for the magnetically assisted removal of methylene blue (MB) from water. The kinetics of adsorption was well predicted using the pseudo-second-order equation. These hybrid materials exhibited high adsorption capacity (530 mg/g maximum) that could be ascribed to surfaces enriched with ester sulfate groups due to extensive grafting of κ-carrageenan over the siliceous domains by using a new surface modification method. The sorbents were long-term colloidal stable and could be easily regenerated after rinsing with KCl aqueous solution. The MB removal efficiency over six consecutive adsorption/desorption cycles was above 97%, which demonstrates the reusability potential and robustness of these hybrid sorbents. This is a new type of adsorbent that promises extensive application in the removal of organic dyes from wastewaters using magnetic separation technologies.

Quantitative Assessment of PM2.5 Sources and Their Seasonal Variation in Krakow

Abstract: In industry areas of Poland such as Silesia or urban sites like Krakow and some other cities, the levels of pollutants frequently breach air quality standards. Particulate matter (PM) is the most important constituent of atmospheric pollution. Beginning on 1st February 2014 until 31st January 2015, the samples of fine particulate matter PM2.5 (aerodynamic diameter of particles less than or equal to 2.5 μm) were collected at a site in the south-eastern Krakow urban background area. During this period, 194 samples were taken. The samples showed daily variation of PM2.5 concentration. From these data, monthly variations were estimated and presented in this paper. Monthly integrated data are more representative for the Krakow urban background and show seasonal variation of PM2.5 pollution. The lowest monthly concentration value was found for August 2014—about 10 μg m−3, the highest for February 2014–70 μg m−3, whereas the average annual value was about 31 μg/m3. Utilizing X-ray fluorescence method, concentrations of 15 elements for each sample were determined and 8 inorganic ions were analyzed by ion chromatography. Additionally, the samples were analyzed for black carbon (BC). Receptor model PMF (positive matrix factorization) was used for source identification and apportionment. The modeling identified six sources and their quantitative contributions to PM2.5 total mass. The following sources were identified: combustion, secondary nitrate and sulfate, biomass burning, industry or/and soil and traffic. Finally, monthly variations of each source are presented.

Are Nitric Acid (HNO3) Digestions Efficient in Isolating Microplastics from Juvenile Fish

Abstract: A standard method for the detection and isolation of microplastics is required to adequately investigate plastic ingestion by juvenile fish. Dissections of juvenile fish guts require precise handling, which can affect the processing time if sample numbers are high. To investigate the efficacy of nitric acid (HNO3) in aiding the isolation of microplastics using whole fish, we digested juvenile glassfish, Ambassis dussumieri (Cuvier, 1828), at room temperature and at 80 °C. For a complete digestion, overnight incubation in 10 mL of 55% analytical-reagent (AR) HNO3 was sufficient for a whole fish of 1 g at room temperature. When coupled with elevated temperature, the digestion time is shortened to a few minutes and larger fish of 3 g can be digested in 30 min. Four of the five types of plastic survived the process, with nylon being the exception. This is a shortfall to the method; however, until a better method replaces it, we still value the use of HNO3 for its simple, inexpensive, swift and complete digestions of whole fish. Four fish species from two feeding guilds were digested using this method to validate its use. The number of plastic particles ingested did not differ between benthic and pelagic species and microplastic fibres comprised the majority of the plastic types found.

Effect of Biochar Amendment and Ageing on Adsorption and Degradation of Two Herbicides

Abstract: Biochar amendment can alter soil properties, for instance, the ability to adsorb and degrade different chemicals. However, ageing of the biochar, due to processes occurring in the soil over time, can influence such biochar-mediated effects. This study examined how biochar affected adsorption and degradation of two herbicides, glyphosate (N-(phosphonomethyl)-glycine) and diuron (3-(3,4-dichlorophenyl)-1,1-dimethylurea) in soil and how these effects were modulated by ageing of the biochar. One sandy and one clayey soil that had been freshly amended with a wood-based biochar (0, 1, 10, 20 and 30% w/w) were studied. An ageing experiment, in which the soil-biochar mixtures were aged for 3.5 months in the laboratory, was also performed. Adsorption and degradation were studied in these soil and soil-biochar mixtures, and compared to results from a soil historically enriched with charcoal. Biochar amendment increased the pH in both soils and increased the water-holding capacity of the sandy soil. Adsorption of diuron was enhanced by biochar amendment in both soils, while glyphosate adsorption was decreased in the sandy soil. Ageing of soil-biochar mixtures decreased adsorption of both herbicides in comparison with freshly biochar-amended soil. Herbicide degradation rates were not consistently affected by biochar amendment or ageing in any of the soils. However, glyphosate half-lives correlated with the Freundlich Kf values in the clayey soil, indicating that degradation was limited by availability there.

Integrated Anaerobic-Aerobic Biodegradation of Multiple Contaminants Including Chlorinated Ethylenes, Benzene, Toluene, and Dichloromethane

Abstract: Complete bioremediation of soils containing multiple volatile organic compounds (VOCs) remains a challenge. To explore the possibility of complete bioremediation through integrated anaerobic-aerobic biodegradation, laboratory feasibility tests followed by alternate anaerobic-aerobic and aerobic-anaerobic biodegradation tests were performed. Chlorinated ethylenes, including tetrachloroethylene (PCE), trichloroethylene (TCE), cis-dichloroethylene (cis-DCE), and vinyl chloride (VC), and dichloromethane (DCM) were used for anaerobic biodegradation, whereas benzene, toluene, and DCM were used for aerobic biodegradation tests. Microbial communities involved in the biodegradation tests were analyzed to characterize the major bacteria that may contribute to biodegradation. The results demonstrated that integrated anaerobic-aerobic biodegradation was capable of completely degrading the seven VOCs with initial concentration of each VOC less than 30 mg/L. Benzene and toluene were degraded within 8 days, and DCM was degraded within 20 to 27 days under aerobic conditions when initial oxygen concentrations in the headspaces of test bottles were set to 5.3% and 21.0%. Dehalococcoides sp., generally considered sensitive to oxygen, survived aerobic conditions for 28 days and was activated during the subsequent anaerobic biodegradation. However, degradation of cis-DCE was suppressed after oxygen exposure for more than 201 days, suggesting the loss of viability of Dehalococcoides sp., as they are the only known anaerobic bacteria that can completely biodegrade chlorinated ethylenes to ethylene. Anaerobic degradation of DCM following previous aerobic degradation was complete, and yet-unknown microbes may be involved in the process. The findings may provide a scientific and practical basis for the complete bioremediation of multiple contaminants in situ and a subject for further exploration.

Field Performance of Bioretention Systems for Runoff Quantity Regulation and Pollutant Removal

Abstract: Bioretention systems are of immense importance as they serve as small “sponges” for cities, cutting stormwater runoff, removing pollution, and using precipitation resources. However, performance data for these facilities are generally lacking, particularly at the field scale. This study investigated the runoff quantity regulation and pollutant removal performance of bioswale and rain garden systems from 2014 to 2017. A performance assessment of these facilities demonstrated that anti-seepage rain garden, bioswale-A, and bioswale-B effectively retained inflow volumes by the filter media, reducing runoff volumes by 54.08, 98.25, and 77.65%, respectively, on average, with only two events of overflowing. According to the water quality data in 24 rainfall events, the main pollutant indexes for the new city include total nitrogen and chemical oxygen demand, and the median values for their respective effluent event median concentrations were 1.29 and 40.13 mg/L for anti-seepage rain garden and 1.68 and 74.00 mg/L for bioswale-B systems. The mean values of pollutant removal of the three bioretention systems, except for infiltration rain garden, were 39.8–59.73% (median = 54.32%), 61.06–72.66% (median = 73.47%), and 76.67%–88.16% (median = 80.64%). Meanwhile, outflow volume of water was found to be most influenced by inflow volumes for the bioswales and anti-seepage rain garden. Mass removals were higher than concentrations owing to water volume attenuation. Based on the data of monitored pollution loads, this study estimated the annual pollutant load removal as 75.45 and 90.7% for anti-seepage rain garden and bioswale-B according to the percent of monitoring rainfall depth in total annual precipitation. This study also established the target pollutant service life model on the basis of accumulated annual load and media adsorption capacity. The results of this study will contribute to a greater understanding of the treatment performance of bioretention systems, assisting in the design, operation, and maintenance of them.

Study on Sorption Characteristics of Uranium onto Biochar Derived from Eucalyptus Wood

Abstract: In this study, the sorption characteristics of U(VI) onto eucalyptus biochar as a function of various operating parameters such as solution pH, initial metal ion concentration, contact time and ionic strength of the medium are reported. Biochar was characterised using various techniques such as CHNS element analysis, Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS). SEM analysis showed the presence of micro- and macropores in the sorbent, and FTIR spectra confirmed the presence of functional groups like carboxylic (−COOH), hydroxyls(−OH), carbonyls(–C=O), etc. Maximum sorption of about 95% is found to occur in the pH range of 5 to 6. U(VI) sorption onto biochar reached equilibrium within 20 min at pH 5.5. The kinetic data were analysed using both pseudo-first-order and pseudo-second-order kinetic models, and the latter is found to be more appropriate to explain the observed kinetics. The equilibrium data were correlated with Langmuir and Freundlich models, and the maximum monolayer adsorption capacity obtained from the Langmuir model was 27.2 mg/g at 293 K. From EDS, FTIR and XPS measurements, it is found that the sorption process involves chemical interaction between the U(VI) and the surface functional groups on the adsorbent. Efficient removal of low level of uranium from ammonium diuranate supernatant demonstrates its utility as sorbent for waste water treatment.

The Impact of Climate Change on Metal Transport in a Lowland Catchment

Abstract: This study investigates the impact of future climate change on heavy metal (i.e., Cd and Zn) transport from soils to surface waters in a contaminated lowland catchment. The WALRUS hydrological model is employed in a semi-distributed manner to simulate current and future hydrological fluxes in the Dommel catchment in the Netherlands. The model is forced with climate change projections and the simulated fluxes are used as input to a metal transport model that simulates heavy metal concentrations and loads in quickflow and baseflow pathways. Metal transport is simulated under baseline climate (“2000–2010”) and future climate (“2090–2099”) conditions including scenarios for no climate change and climate change. The outcomes show an increase in Cd and Zn loads and the mean flux-weighted Cd and Zn concentrations in the discharged runoff, which is attributed to breakthrough of heavy metals from the soil system. Due to climate change, runoff enhances and leaching is accelerated, resulting in enhanced Cd and Zn loads. Mean flux-weighted concentrations in the discharged runoff increase during early summer and decrease during late summer and early autumn under the most extreme scenario of climate change. The results of this study provide improved understanding on the processes responsible for future changes in heavy metal contamination in lowland catchments.