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Current opinion: What is a nanoplastic?
2018
Gigault, Julien | Halle, Alexandra Ter | Baudrimont, Magalie | Pascal, Pierre-Yves | Gauffre, Fabienne | Phi, Thuy-Linh | El Hadri, Hind | Grassl, Bruno | Reynaud, Stéphanie | Géosciences Rennes (GR) ; Université de Rennes (UR)-Institut national des sciences de l'Univers (INSU - CNRS)-Observatoire des Sciences de l'Univers de Rennes (OSUR) ; Université de Rennes (UR)-Institut national des sciences de l'Univers (INSU - CNRS)-Université de Rennes 2 (UR2)-Centre National de la Recherche Scientifique (CNRS)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)-Institut national des sciences de l'Univers (INSU - CNRS)-Université de Rennes 2 (UR2)-Centre National de la Recherche Scientifique (CNRS)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)-Centre National de la Recherche Scientifique (CNRS) | Chimie des colloïdes, polymères & assemblages complexes (Softmat) ; Institut de Chimie de Toulouse (ICT) ; Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3) ; Université de Toulouse (UT)-Université de Toulouse (UT)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)-Institut National Polytechnique (Toulouse) (Toulouse INP) ; Université de Toulouse (UT)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3) ; Université de Toulouse (UT)-Université de Toulouse (UT)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)-Institut National Polytechnique (Toulouse) (Toulouse INP) ; Université de Toulouse (UT)-Fédération de Recherche Fluides, Energie, Réacteurs, Matériaux et Transferts (FERMAT) ; Institut National des Sciences Appliquées - Toulouse (INSA Toulouse) ; Institut National des Sciences Appliquées (INSA)-Université de Toulouse (UT)-Institut National des Sciences Appliquées (INSA)-Université de Toulouse (UT)-Université Toulouse III - Paul Sabatier (UT3) ; Université de Toulouse (UT)-Centre National de la Recherche Scientifique (CNRS)-Institut National Polytechnique (Toulouse) (Toulouse INP) ; Université de Toulouse (UT)-Institut National des Sciences Appliquées - Toulouse (INSA Toulouse) ; Institut National des Sciences Appliquées (INSA)-Université de Toulouse (UT)-Institut National des Sciences Appliquées (INSA)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS) | Environnements et Paléoenvironnements OCéaniques (EPOC) ; Observatoire aquitain des sciences de l'univers (OASU) ; Université Sciences et Technologies - Bordeaux 1 (UB)-Institut national des sciences de l'Univers (INSU - CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université Sciences et Technologies - Bordeaux 1 (UB)-Institut national des sciences de l'Univers (INSU - CNRS)-Centre National de la Recherche Scientifique (CNRS)-École Pratique des Hautes Études (EPHE) ; Université Paris Sciences et Lettres (PSL)-Université Paris Sciences et Lettres (PSL)-Centre National de la Recherche Scientifique (CNRS) | Adaptation aux milieux extrêmes ; Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS) | Institut des Sciences Chimiques de Rennes (ISCR) ; Université de Rennes (UR)-Institut National des Sciences Appliquées - Rennes (INSA Rennes) ; Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Ecole Nationale Supérieure de Chimie de Rennes (ENSCR)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS) | Institut des sciences analytiques et de physico-chimie pour l'environnement et les materiaux (IPREM) ; Université de Pau et des Pays de l'Adour (UPPA)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS) | This work was supported by the French National Agency of Research (ANR-17-CE34-0008: PEPSEA) and the Interdisciplinary Mission of the French National Center for Scientific Research (CNRS). | ANR-17-CE34-0008,PEPSEA,Nanoparticules de plastiques dans l'environnement: source, impact et prédiction(2017)
International audience | With the large amount of attention being given to microplastics in the environment, several researchers have begun to consider the fragmentation of plastics down to lower scales (i.e., the sub-micrometer scale). The term “nanoplastics” is still under debate, and different studies have set the upper size limit at either 1000 nm or 100 nm. The aim of the present work is to propose a definition of nanoplastics, based on our recently published and unpublished research definition of nanoplastics. We define nanoplastics as particles unintentionally produced (i.e. from the degradation and the manufacturing of the plastic objects) and presenting a colloidal behavior, within the size range from 1 to 1000 nm.
Show more [+] Less [-]Uranium (VI) transport in saturated heterogeneous media: Influence of kaolinite and humic acid
2018
Chen, Chong | Zhao, Kang | Shang, Jianying | Liu, Chongxuan | Wang, Jin | Yan, Zhifeng | Liu, Kesi | Wu, Wenliang
Natural aquifers typically exhibit a variety of structural heterogeneities. However, the effect of mineral colloids and natural organic matter on the transport behavior of uranium (U) in saturated heterogeneous media are not totally understood. In this study, heterogeneous column experiments were conducted, and the constructed columns contained a fast-flow domain (FFD) and a slow-flow domain (SFD). The effect of kaolinite, humic acid (HA), and kaolinite/HA mixture on U(VI) retention and release in saturated heterogeneous media was examined. Media heterogeneity significantly influenced U fate and transport behavior in saturated subsurface environment. The presence of kaolinite, HA, and kaolinite/HA enhanced the mobility of U in heterogeneous media, and the mobility of U was the highest in the presence of kaolinite/HA and the lowest in the presence of kaolinite. In the presence of kaolinite, there was no difference in the amount of U released from the FFD and SFD. However, in the presence of HA and kaolinite/HA, a higher amount of U was released from the FFD. The findings in this study showed that medium structure and mineral colloids, as well as natural organic matter in the aqueous phase had significant effects on U transport and fate in subsurface environment.
Show more [+] Less [-]Role of rain intensity and soil colloids in the retention of surfactant-stabilized silver nanoparticles in soil
2018
Makselon, Joanna | Siebers, Nina | Meier, Florian | Vereecken, H. (Harry) | Klumpp, Erwin
Undisturbed outdoor lysimeters containing arable loamy sand soil were used to examine the influence of either heavy rain events (high frequency of high rain intensity), steady rain (continuous rainfall of low rain intensity), and natural rainfall on the transport and retention of surfactant-stabilized silver nanoparticles (AgNP). In addition, the AgNP–soil associations within the Ap horizon were analyzed by means of particle-size fractionation, asymmetrical flow field-flow fractionation coupled with UV/Vis-detection and inductively coupled plasma mass spectrometer (AF4-UV/Vis-ICP-MS), and transmission electron microscopy coupled to an energy-dispersive X-ray (TEM-EDX) analyzer. The results showed that AgNP breakthrough for all rain events was less than 0.1% of the total AgNP mass applied, highlighting that nearly all AgNP were retained in the soil. Heavy rain treatment and natural rainfall revealed enhanced AgNP transport within the Ap horizon, which was attributed to the high pore water flow velocities and to the mobilization of AgNP–soil colloid associations. Particle-size fractionation of the soil revealed that AgNP were present in each size fraction and therefore indicated strong associations between AgNP and soil. In particular, water-dispersible colloids (WDC) in the size range of 0.45–0.1 μm were found to exhibit high potential for AgNP attachment. The AF4-UV/Vis-ICP-MS and TEM-EDX analyses of the WDC fraction confirmed that AgNP were persistent in soil and associated to soil colloids (mainly composed of Al, Fe, Si, and organic matter). These results confirm the particularly important role of soil colloids in the retention and remobilization of AgNP in soil. Furthermore, AF4-UV/Vis-ICP-MS results indicated the presence of single, homo-aggregated, and small AgNP probably due to dissolution.
Show more [+] Less [-]Does sulfur fertilizer influence Cu migration and transformation in colloids of soil pore water from the rice (Oryza sativa L.) rhizosphere?
2018
Sun, Lijuan | Xue, Yong | Peng, Cheng | Xu, Chen | Shi, Jiyan
Colloids are ubiquitous in soils, and it has been reported that colloids can act as carriers to increase the mobility of poorly soluble contaminants in subsurface environments. Addition of sulfur (S) fertilizer greatly influences on heavy metal behavior in paddy soil, while the influence of S fertilizer on Cu migration and transformation in colloids of soil pore water has not yet been studied. The influence of S fertilizer (S⁰ and Na₂SO₄) applied in paddy soils on Cu migration and transformation in colloids of soil pore water from the rice rhizosphere region was explored in this study. The speciation of Cu in colloids of soil pore water from the rice rhizosphere region was explored by advanced synchrotron-based X-ray absorption near-edge spectroscopy (XANES) techniques. The morphology of colloids was characterized by field emission scanning electron microscopy coupled to energy dispersive X-ray spectroscopy (SEM-EDX). At a depth of 20 cm, the concentration of Cu in colloids of the rhizosphere soil pore water in the control was 2.4- and 6.5- fold higher than that in treatments of S⁰ and Na₂SO₄, respectively. The colloids in soil pore water were all positively charged, ranging from 2.4 to 7.8 mV, and the size of colloids was 440–740 nm. The proportion of Fe in colloids in the rhizosphere region decreased with S fertilizer application, while the proportions of C and O increased. Sulfur fertilizer application, increased the proportion of Cu-Cysteine, while the proportion of Cu₂S decreased in soil colloids. In conclusion, application of sulfur fertilizer in paddy soil decreased the Cu concentration in soil pore water and colloids of the rhizosphere region, thereby decreasing the vertical migration of Cu in soil pore water.
Show more [+] Less [-]Effects of the natural colloidal particles from one freshwater lake on the photochemistry reaction kinetics of ofloxacin and enrofloxacin
2018
Cheng, Dengmiao | Liu, Xinhui | Li, Jinpeng | Feng, Yao | Wang, Juan | Li, Zhaojun
Understanding the effect of natural colloidal particles (NCPs) on the photochemistry of organic pollutants is crucial to predict the environmental persistence and fate of them in surface waters, and it is, yet, scarcely elucidated. In this study, the pre-filtered surface water (through a 1 μm capsule filter) from Baiyangdian Lake was further separated into four different size NCPs: F1 (0.65–1.0 μm), F2 (100 kD-0.65 μm), F3 (10–100 kD) and F4 (1–10 kD) by cross-flow ultrafiltration (CFUF), and the photochemical kinetics and mechanisms of ofloxacin (OFL) and enrofloxacin (ENR) were investigated in the presence of those particles under simulated sunlight. Results showed that OFL and ENR underwent both direct and indirect photolysis in F1-F4 solutions, and the observed pseudo first-order rate constants (kobs) for target compounds differed depending on the size of NCPs. Direct photolysis accounted for >50% of the degradation in all cases and was the dominant degradation pathway for the two target antibiotics with the exception of OFL in F1 solution. Except for ENR in both F3 and F4 solutions, nearly all NCPs enhanced the degradation of both target compounds by indirect photolytic pathways, especially in F1 solution that showed the largest reactivity for OFL and ENR, promoting the reactions by 63% and 41%, respectively. The excited state colloidal organic matter (3COM∗) plays a significant role in the indirect photolysis, and the adsorptions of OFL and ENR to NCPs were likely to have a pronounced effect in the photochemistry process. Pearson's correlations analysis showed that the kobs(OFL) was significant positive correlated with binding of Fe (r = 0.963, P < 0.05), and the kobs(ENR) was significant positive correlated with the adsorption percentage of OFL (r = 0.999, P < 0.01).This paper has demonstrated that different size NCPs showed the different photochemical contribution to the reaction rate for OFL and ENR.
Show more [+] Less [-]Selenium in surface waters of the lower Athabasca River watershed: Chemical speciation and implications for aquatic life
2018
Donner, Mark W. | Cuss, Chad W. | Poesch, Mark | Sinnatamby, R Nilo | Shotyk, William | Siddique, Tariq
Selenium in the lower Athabasca River (Alberta, Canada) is of concern due to potential inputs from the weathering of shallow bitumen deposits and emissions from nearby surface mines and upgraders. Understanding the source of this Se, however, is complicated by contributions from naturally saline groundwater and organic matter-rich tributaries. As part of a two-year multi-disciplinary study to assess natural and anthropogenic inputs, Se and its chemical speciation were determined in water samples collected along a ∼125 km transect of the Athabasca River and associated tributaries. Selenium was also determined in the muscle of Trout-perch (Percopsis omiscomaycus), a non-migratory fish species, that were sampled from selected locations. Dissolved (<0.45 μm) Se in the Athabasca River was consistently low in 2014 (0.11 ± 0.02 μg L⁻¹; n = 14) and 2015 (0.16 ± 0.02 μg L⁻¹; n = 21), with no observable increase from upstream to downstream. Selenate was the predominant inorganic form (∼60 ng L⁻¹) and selenite was below detection limits at most locations. The average concentration of Se in Trout-perch muscle was 2.2 ± 0.4 mg kg⁻¹ (n = 34), and no significant difference (p > 0.05) was observed between upstream and midstream (industrial) or downstream reaches. Tributary waters contained very low concentrations of Se (typically < 0.1 μg L⁻¹), which was most likely present in the form of dissolved organic colloids.
Show more [+] Less [-]Classification of oil–particle interactions in aqueous environments: Aggregate types depending on state of oil and particle characteristics
2018
Boglaienko, Daria | Tansel, Berrin
There are significant differences in the aggregation mechanisms and types of aggregates that form by oil-particle interactions in marine and laboratory environments depending on the state of oil (i.e., dissolved, emulsified, floating), size and type of particles involved (i.e., colloidal, granular, organic, inorganic), oil-particle interaction mechanisms, and settling/suspension characteristics. Distinct characteristics of oil-particle aggregates that form by interaction of granular particles with floating oil separate them from the well-known oil-colloidal particle aggregates (OcPA), which are sometimes called Pickering emulsions. Unlike OcPA, which involve emulsified oil (entrained oil droplets suspended in the water column) and colloidal particles, the oil-granular particle aggregates (OgPA) involve the floating oil and granular particles. Here, to clarify the differences and similarities between the two types of aggregates (OcPA and OgPA), we present classification of oil aggregates, drawing attention to important characteristics of OcPA, marine oil snow (MOS), and OgPA.
Show more [+] Less [-]Effective sorption of atrazine by biochar colloids and residues derived from different pyrolysis temperatures
2018
Yang, Fan | Gao, Yan | Sun, Lili | Zhang, Shuaishuai | Li, Jiaojiao | Zhang, Ying
Biochar has attracted much attention, which owns many environmental and agronomic benefits, including carbon sequestration, improvement of soil quality, and immobilization of environmental contaminants. Biochar has been also investigated as an effective sorbent in recent publications. Generally, biochar particles can be divided into colloids and residues according to particle sizes, while understanding of adsorption capacities towards organic pollutants in each section is largely unknown, representing a critical knowledge gap in evaluations on the effectiveness of biochar for water treatment application. Scanning electron microscopy (SEM) images, X-ray diffraction (XRD), Raman spectra, Fourier-transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), and Brunauer-Emmett-Teller (BET) method are used to examine the structures and surface properties of biochar colloids and residues derived from corn straws prepared at different pyrolysis temperatures. Also, their roles in atrazine (a typical organic pollutant) removal are investigated by batch adsorption experiments and fitted by different kinetic and thermodynamic models, respectively. The adsorption capacities of biochar colloids are much more than those of residues, resulting from the colloids containing abundant oxygen functional groups and mineral substances, and the adsorption capacities of biochar colloids and residues increase with the increase of pyrolysis temperatures. The highest adsorption performance of 139.33 mg g⁻¹ can be obtained in biochar colloids prepared at 700 °C, suggesting the important functions of biochar colloids in the application of atrazine removal by biochar.
Show more [+] Less [-]Removal of macro-pollutants in oily wastewater obtained from soil remediation plant using electro-oxidation process
2018
Zolfaghari, Mehdi | Drogui, Patrick | Blais, JeanFrançois
Electro-oxidation process by niobium boron-doped diamond (Nb/BDD) electrode was used to treat non-biodegradable oily wastewater provided from soil leachate contaminated by hydrocarbons. Firstly, the diffusion current limit and mass transfer coefficient was experimentally measured (7.1 mA cm⁻² and 14.7 μm s⁻¹, respectively), in order to understand minimum applied current density. Later on, the oxidation kinetic model of each pollutant was investigated in different current densities ranged between 3.8 and 61.5 mA cm⁻². It was observed that direct oxidation was the main removal mechanism of organic and inorganic carbon, while the indirect oxidation in higher current density was responsible for nitrogen oxidation. Hydrocarbon in the form of colloidal particles could be removed by electro-flotation. On the other hand, electro-decomposition on the surface of cathode and precipitation by hydroxyl ions were the utmost removal pathway of metals. According to the initial experiments, operating condition was further optimized by central composite design model in different current density, treatment time, and electrolyte addition, based on the best responses on the specific energy consumption (SEC), chemical oxygen demand (COD), and total organic carbon (TOC) removal efficiency. Unde r optimum operating condition (current density = 23.1 mA cm⁻², time = 120 min, Ti/Pt as a cathode, and Nb/BDD as the anode), electro-oxidation showed the following removal efficiencies: COD (84.6%), TOC (68.2%), oil and grease (99%), color (87.9%), total alkalinity (92%), Nₜₒₜ (18%), NH₄⁺ (31%), Ca (66.4%), Fe (71.1%), Mg (41.4%), Mn (78.1%), Pₜₒₜ (75%), S (67.1%), and Si (19.1%). Graphical abstract Environmental significance statement Soil treatment facilities are rapidly grown throughout the world, especially in North America due to its intense industrialization. High water content soil in humid area like Canada produces significant amount of leachate which is difficult to remove by physical and biological processes. Current treatment facility was modified by applying the electro-chemical oxidation process. The kinetic models of each macro-pollutant included carbon, nitrogen, phosphorous, and metals were developed to investigate their oxidation mechanism (graphical abstract). The efficiency of treatment was monitored in order to optimize the decisive operating parameters of electro-oxidation process. The result of this article could pave the way of future investigation on efficient treatment of variety of oily wastewater.
Show more [+] Less [-]Magnetic nanocellulose from olive industry solid waste for the effective removal of methylene blue from wastewater
2018
Jodeh, Shehdeh | Hamed, Othman | Melhem, Abeer | Salghi, Rachid | Jodeh, Diana | Azzaoui, Khalil | Benmassaoud, Yassine | Murtada, Khaled
The work shown in this article demonstrate a novel example of converting olive industry solid waste (OISW) into a magnetic cellulose nanocrystalline (MNCs) to serve as selective magnetic sorbents for methylene blue. Olive industry solid waste contains about 40% cellulose. The cellulose was extracted in a powder form from olive industry solid waste by subjecting it to a multistep pulping and bleaching process. The extracted powder cellulose was then converted to nanocrystalline cellulose (NCs) by acid hydrolysis. The NCs were then treated with a solution of FeCl₃.6H₂O, FeSO₄, and H₂O by a colloidal suspension method which produced free-flowing porous MNCs. The produced MNCs are characterized by several spectroscopic and analytical techniques such as SEM, TEM, XRD, FTIR VSM, and TGA. The efficiency of the three polymers cellulose powder, NCs, and MNCs toward extracting methylene blue (MB) from water was evaluated. Cellulose powder and NCs showed acceptable tendency for methylene blue. However, MNCs showed excellent extraction efficiency toward MB. The thermodynamic studies revealed a spontaneous adsorption of MB by MNCs at various temperatures. The spontaneous adsorption could be attributed to the electrostatic interaction and H-bonding between MNCs and MB. However, the interaction between cellulose, NCs, and MB is limited to the H-bonding.
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