Preparation of Nanosized Hematite Particles by Mechanical Activation of Goethite Samples

Nanosized single crystals of hematite with a very narrow particle size distribution were prepared by mechanical activation of two different goethite samples. Both goethite samples transformed completely into hematite after 70 h grinding time. Transmission electron microscopy showed that the final particles were spherical in shape and of ∼17 nm average particle size. This particle size was coincident with that estimated from specific surface measurements, indicating that the hematite samples consisted of nonporous and nonaggregated particles. The crystallite size, calculated from the broadening of the XRD peaks, in the hematite samples indicated that particles consisted of single crystals. No influence of the precursor was observed in the products, so both goethite samples yielded identical rounded single crystals with a narrow particle size distribution.     

Constructive modification of conducting polyaniline characteristics in unusual proportion through nanomaterial blend formation with the neutral polymer poly(vinyl pyrrolidone)

The present work reports an investigation on the modification of conducting polyaniline (PANI) characteristics favorably on blending with the neutral polymer, poly(vinyl pyrrolidone) (PVP) in a systematic variation of their molar ratios (aniline : PVP = 4 : 1, 2 : 1, 1 : 1, 1 : 2, and 1 : 3). Prepared by precipitation technique by conventional in situ chemical oxidative polymerization with ammonium peroxodisulfate in aqueous H₂SO₄ medium (pH 1.0), these materials have nanometer sizes (～ 50–200 nm) and, depending on the molar ratios, exhibit a distinct deviation in physicochemical characteristics from those of pristine PANI prepared in the identical condition. A gradual trend in characteristics is noticed in first three PANI–PVP blends, while an abnormal hike in conductivity, unusual spectral features in IR and UV–vis, hardened nature, and induction of characteristic morphology, crystallinity, and thermal stability are associated with the last two blends that have excess PVP. Thus a division of two sets of nanoblends, one set with less or equal content of PVP and another with excess of PVP, emerges. Evidently, PVP has a tuning effect on PANI through its dopant, supporting matrix and interpenetrating steric stabilizer acts in proportion quite unusual to its neutral nature. The study altogether brings to light a simple way of modification of PANI characteristics by conventional method of blend synthesis. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Effects of solvents on electrospun polymeric fibers: preliminary study on polystyrene

Six solvents [acetic acid, acetonitrile, m‐cresol, toluene, tetrahydrofuran (THF) and dimethylformamide (DMF)] with different properties (eg density, boiling point, solubility parameter, dipole moment and dielectric constant) were used to prepare electrospun polystyrene (PS) fibers. Fiber diameters were found to decrease with increasing density and boiling point of the solvents. A large difference between the solubility parameters of PS and the solvent was responsible for the bead‐on‐string morphology observed. Productivity of the fibers (the numbers of fiber webs per unit area per unit time) increased with increasing dielectric constant and dipole moment of the solvents. Among the solvents studied, DMF was the best solvent that provided PS fibers with highest productivity and optimal morphological characteristics. The beadless, well‐aligned PS fibers with a diameter of ca 0.7 µm were produced from the solution of 10 % (w/v) of PS in DMF at an applied electrostatic field of 15 kV/10 cm, a nitrogen flow rate of 101 ml min^?1 and a rotational speed of the collector of 1500 rev min^?1. Copyright © 2004 Society of Chemical Industry     

Transmission Electron Microscopy and the Science of Carbon Nanomaterials

Carbon is a unique and versatile element that is capable of forming different architectures at nanoscale. The element has become a key component in nanoscience and nanotechnology. Transmission electron microscopy (TEM) acts as “our eyes” enabling us not only to reveal the morphology, but also to provide structural, chemical and electronic information of nanocarbon on the atomic level. In fact, except for fullerene, nearly all types of carbon nanomaterials were discovered by TEM, such as carbon nanotubes, carbon nanocones, and graphene‐like nanocarbon. It cannot be imagined what nanoscience and nanotechnology would be without the contributions of TEM. Herein, the “interaction” between TEM and the science of carbon nanomaterials is reviewed and it is demonstrated for some selected examples that TEM provides a dramatic driving force for the development of nanocarbon science.     

Lab‐on‐a‐Chip‐Based High‐Throughput Screening of the Genotoxicity of Engineered Nanomaterials

The continuous increasing of engineered nanomaterials (ENMs) in our environment, their combinatorial diversity, and the associated genotoxic risks, highlight the urgent need to better define the possible toxicological effects of ENMs. In this context, we present a new high‐throughput screening (HTS) platform based on the cytokinesis‐block micronucleus (CBMN) assay, lab‐on‐chip cell sorting, and automated image analysis. This HTS platform has been successfully applied to the evaluation of the cytotoxic and genotoxic effects of silver nanoparticles (AgNPs) and silica nanoparticles (SiO₂NPs). In particular, our results demonstrate the high cyto‐ and genotoxicity induced by AgNPs and the biocompatibility of SiO₂NPs, in primary human lymphocytes. Moreover, our data reveal that the toxic effects are also dependent on size, surface coating, and surface charge. Most importantly, our HTS platform shows that AgNP‐induced genotoxicity is lymphocyte sub‐type dependent and is particularly pronounced in CD2+ and CD4+ cells.     

Isomeric Routes to Schiff‐Base Single‐layered Covalent Organic Frameworks

With graphene‐like topology and designable functional moieties, single‐layered covalent organic frameworks (sCOFs) have attracted enormous interest for both fundamental research and application prospects. As the growth of sCOFs involves the assembly and reaction of precursors in a spatial defined manner, it is of great importance to understand the kinetics of sCOFs formation. Although several large families of sCOFs and bulk COF materials based on different coupling reactions have been reported, the synthesis of isomeric sCOFs by exchanging the coupling reaction moieties on precursors has been barely explored. Herein, a series of isomeric sCOFs based on Schiff‐base reaction is designed to understand the effect of monomer structure on the growth kinetics of sCOFs. The distinctly different local packing motifs in the mixed assemblies for the two isomeric routes closely resemble to those in the assemblies of monomers, which affect the structural evolution process for highly ordered imine‐linked sCOFs. In addition, surface diffusion of monomers and the molecule‐substrate interaction, which is tunable by reaction temperature, also play an important role in structural evolutions. This study highlights the important roles of monomer structure and reaction temperature in the design and synthesis of covalent bond connected functional nanoporous networks.     

Nanomaterial‐enabled Rapid Detection of Water Contaminants

Water contaminants, e.g., inorganic chemicals and microorganisms, are critical metrics for water quality monitoring and have significant impacts on human health and plants/organisms living in water. The scope and focus of this review is nanomaterial‐based optical, electronic, and electrochemical sensors for rapid detection of water contaminants, e.g., heavy metals, anions, and bacteria. These contaminants are commonly found in different water systems. The importance of water quality monitoring and control demands significant advancement in the detection of contaminants in water because current sensing technologies for water contaminants have limitations. The advantages of nanomaterial‐based sensing technologies are highlighted and recent progress on nanomaterial‐based sensors for rapid water contaminant detection is discussed. An outlook for future research into this rapidly growing field is also provided.