Correction: Factors impacting the aggregation/agglomeration and photocatalytic activity of highly crystalline spheroid- and rod-shaped TiO nanoparticles in aqueous solutions.

Correction for 'Factors impacting the aggregation/agglomeration and photocatalytic activity of highly crystalline spheroid- and rod-shaped TiO nanoparticles in aqueous solutions' by Thomas Degabriel, Elodie Colaço , , 2018, , 12898-12907, https://doi.org/10.1039/C7CP08054A.

Hierarchical Collagen-Hydroxyapatite Nanostructures Designed through Layer-by-Layer Assembly of Crystal-Decorated Fibrils.

A comprehensive understanding of the mechanism by which type I collagen (Col) interacts with hydroxyapatite nanoparticles (Hap NPs) in aqueous solutions is a pivotal step for guiding the design of biologically relevant nanocomposites with controlled hierarchical structure. In this paper we use a variety of Hap NPs differing by their shape (rod vs platelet) and their size (∼30 vs ∼130 nm) and investigate their mechanism(s) of interaction with collagen. The addition of collagen to the Hap suspensions induces different effects that strongly depend on the nanoparticle type.

Factors impacting the aggregation/agglomeration and photocatalytic activity of highly crystalline spheroid- and rod-shaped TiO nanoparticles in aqueous solutions.

We investigate the characteristics, fate and photocatalytic activity of spheroid- and rod-shaped TiO2 nano-crystals in aqueous solutions to better understand their behaviour in media of biological and environmental interest. For this purpose, the potential of a solvothermal method in synthesizing highly crystalline nanoparticles and tuning their sizes/shapes is explored. Spheroid- and rod-shaped nanoparticles are successfully obtained with different aspect ratios, while keeping their structures as well as their cross-sectional areas identical.

AGNES at vibrated gold microwire electrode for the direct quantification of free copper concentrations.

The free metal ion concentration and the dynamic features of the metal species are recognized as key to predict metal bioavailability and toxicity to aquatic organisms. Quantification of the former is, however, still challenging. In this paper, it is shown for the first time that the concentration of free copper (Cu(2+)) can be quantified by applying AGNES (Absence of Gradients and Nernstian equilibrium stripping) at a solid gold electrode.

Polymer functionalized nanocomposites for metals removal from water and wastewater: An overview.

Pollution by metal and metalloid ions is one of the most widespread environmental concerns. They are non-biodegradable, and, generally, present high water solubility facilitating their environmental mobilisation interacting with abiotic and biotic components such as adsorption onto natural colloids or even accumulation by living organisms, thus, threatening human health and ecosystems. Therefore, there is a high demand for effective removal treatments of heavy metals, making the application of adsorption materials such as polymer-functionalized nanocomposites (PFNCs), increasingly attractive.

Manufactured nanoparticles in the aquatic environment-biochemical responses on freshwater organisms: A critical overview.

The enormous investments in nanotechnology have led to an exponential increase of new manufactured nano-enabled materials whose impact in the aquatic systems is still largely unknown. Ecotoxicity and nanosafety studies mostly resulted in contradictory results and generally failed to clearly identify biological patterns that could be related specifically to nanotoxicity. Generation of reactive oxygen species (ROS) is one of the most discussed nanotoxicity mechanism in literature.

The role of charged polymer coatings of nanoparticles on the speciation and fate of metal ions in the environment.

Determining the environmental risk of metals requires an in-depth understanding of the environmental matrices composition, which currently also includes the presence of manufactured metallic nanoparticles (NPs) usually, stabilized by a polymer surface coating. As a consequence, is necessary to take into account effects of the NP core, the polymer surface coating and their mutual interaction as well as with other environmental components. The release of metal ions from metallic NPs is a well-known outcome, however, the effect of the presence of the NP polymer coating in the NPs solubilization mechanism is not well understood.

Bioavailability of cadmium and biochemical responses on the freshwater bivalve Corbicula fluminea--the role of TiO₂ nanoparticles.

The increasing and widespread applications of TiO2 engineered nanoparticles (nTiO2) led to the release of these materials into aquatic environments and consequently a change on the assessment of the environmental risk of trace metals. In this work, the role of two commercial nTiO2 with distinct crystalline phases and sizes (nTiO2-P25: 80% anatase+20% rutile, d=20nm; nTiO2-NA: 100% anatase, d=5 nm; 0.1 and 1.

The effects of different coatings on zinc oxide nanoparticles and their influence on dissolution and bioaccumulation by the green alga, C. reinhardtii.

Determining the environmental risk of nanoparticles (NPs) requires an in-depth understanding of the NP core, the particle surface coatings and the interactions of the two with environmental matrices. Non-coated ZnO NPs (nZnO) are known to release ionic Zn, contributing directly to the toxicity of these particles. On the other hand, relatively less data are available for particles that have coatings designed to increase particle stability.

Transcriptome sequencing (RNA-seq) analysis of the effects of metal nanoparticle exposure on the transcriptome of Chlamydomonas reinhardtii.

The widespread use of nanoparticles (NPs) raises concern over their potential toxicological effects in humans and ecosystems. Here we used transcriptome sequencing (RNA-seq) to evaluate the effects of exposure to four different metal-based NPs, nano-Ag (nAg), nano-TiO2 (nTiO2), nano-ZnO (nZnO), and CdTe/CdS quantum dots (QDs), in the eukaryotic green alga Chlamydomonas reinhardtii. The transcriptome was characterized before and after exposure to each NP type.

Stability of core/shell quantum dots--role of pH and small organic ligands.

The improvement of knowledge about the toxicity and even processability, and stability of quantum dots (QD) requires the understanding of the relationship between the QD binding head group, surface structure, and interligand interaction. The scanned stripping chronopotentiometry and absence of gradients and Nernstian equilibrium stripping techniques were used to determine the concentration of Cd dissolved from a polyacrylate-stabilized CdTe/CdS QD. The effects of various concentrations of small organic ligands such as citric acid, glycine, and histidine and the roles of pH (4.

Bioaccumulation and effects of CdTe/CdS quantum dots on Chlamydomonas reinhardtii - nanoparticles or the free ions?

In order to properly assess the environmental risk of engineered nanoparticles (ENP), it is necessary to determine their fate (including dissolution, aggregation, and bioaccumulation) under representative environmental conditions. CdTe/CdS quantum dots (QD), such as those used in medical imaging, are known to release Cd(2+) due (mainly) to the dissolution of their outer shell. In this study, Chlamydomonas reinhardtii was exposed to either a soluble Cd salt or QD at similar concentrations of total Cd.

Characterizing manufactured nanoparticles in the environment: multimethod determination of particle sizes.

Sizes of stabilized (24 h) nanoparticle suspensions were determined using several state-of-the-art analytical techniques (transmission electron microscopy; atomic force microscopy; dynamic light scattering; fluorescence correlation spectroscopy; nanoparticle tracking analysis; flow field flow fractionation). Theoretical and analytical considerations were evaluated, results were compared, and the advantages and limitations of the techniques were discussed. No "ideal" technique was found for characterizing manufactured nanoparticles in an environmental context as each technique had its own advantages and limitations.

Deposition of TiO2 nanoparticles onto silica measured using a quartz crystal microbalance with dissipation monitoring.

Titanium dioxide (TiO2) nanoparticles introduced into subsurface environments may lead to contamination of drinking water supplies and can act as colloidal carriers for sorbed contaminants. A model laboratory system was used to examine the influence of water chemistry on the physicochemical properties of TiO2 nanoparticles and their deposition. Deposition rates of TiO2 particles onto a silica surface were measured over a broad range of solution conditions (pH and ionic strength) using a quartz crystal microbalance with energy dissipation monitoring (QCM-D).

Aggregation of titanium dioxide nanoparticles: role of a fulvic acid.

The increasing use of nanomaterials in consumer products has led to increased concerns abouttheir potential environmental and health impacts. To better understand the transport, fate, and behavior of nanoparticles in aquatic systems, it is essential to understand their interactions with different components of natural waters including natural organic matter over a broad range of physicochemical conditions. Fluorescence correlation spectroscopy was used to determine the diffusion coefficients of TiO2 nanoparticles having a nominal size of 5 nm.

Copper removal by algal biomass: biosorbents characterization and equilibrium modelling.

The general principles of Cu(II) binding to algal waste from agar extraction, composite material and algae Gelidium, and different modelling approaches, are discussed. FTIR analyses provided a detailed description of the possible binding groups present in the biosorbents, as carboxylic groups (D-glucuronic and pyruvic acids), hydroxyl groups (cellulose, agar and floridean starch) and sulfonate groups (sulphated galactans). Potentiometric acid-base titrations showed a heterogeneous distribution of two major binding groups, carboxyl and hydroxyl, following the quasi-Gaussian affinity constant distribution suggested by Sips, which permitted to estimate the maximum amount of acid functional groups (0.

Application of permeation liquid membrane and scanned stripping chronopotentiometry to metal speciation analysis of colloidal complexes.

The potential of permeation liquid membrane (PLM) to obtain dynamic metal speciation information for colloidal complexes is evaluated by measurements of lead(II) and copper(II) complexation by carboxyl modified latex nanospheres of different radii (15, 35, 40 and 65 nm). The results are compared with those obtained by a well characterized technique: stripping chronopotentiometry at scanned deposition potential (SSCP). Under the PLM conditions employed, and for large particles or macromolecular ligands, membrane diffusion is the rate-limiting step.