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The potential toxicity of carbon nanotubes (CNTs) has been compared to pathogenic fibres such as asbestos. It is important to test this hypothesis to ascertain safe methods for CNT production, handling and disposal. In this study aspects reported to contribute to CNT toxicity were assessed: length, aspect ratio, iron content and crystallinity; with responses compared to industrially produced MWCNTs and toxicologically relevant materials such as asbestos. The impacts of these particles on a range of macrophage models in vitro were assessed due to the key role of macrophages in particle clearance and particle/fibre-induced disease. Industrially produced and long MWCNTs were cytotoxic to cells, and were potent in inducing pro-inflammatory and pro-fibrotic immune responses. Short CNTs did not induce any cytotoxicity. Frustrated phagocytosis was most evident in response to long CNTs, as was respiratory burst and reduction in phagocytic ability. Short CNTs, metal content and crystallinity had less or no influence on these endpoints, suggesting that many responses were fibre-length dependent. This study demonstrates that CNTs are potentially pathogenic, as they were routinely found to induce detrimental responses in macrophages greater than those induced by asbestos at the same mass-based dose., (Copyright © 2015 Elsevier Ltd. All rights reserved.)

The complex structure of the macroscopic assemblies of carbon nanotubes and variable intrinsic piezoresistivity of nanotubes themselves lead to highly interesting piezoresistive performance of this new type of conductive material. Here, we present an in-depth study of the piezoresistive effect in carbon nanotube fibers, i.e., yarnlike assemblies made purely of aligned carbon nanotubes, which are expected to find applications as electrical and electronic materials. The resistivity changes of carbon nanotube fibers were measured on initial loading, through the elastic/plastic transition, on cyclic loading and on stress relaxation. The various regimes of stress/strain behavior were modeled using a standard linear solid model, which was modified with an additional element in series to account for the observed creep behavior. On the basis of the experimental and modeling results, the origin of piezoresistivity is discussed. An additional effect on the resistivity was found as the fiber was held under load which led to observations of the effect of humidity and the associated water adsorption level on the resistivity. We show that the equilibrium uptake of moisture leads to the decrease in gauge factor of the fiber decrease, i.e., the reduction in the sensitivity of fiber resistivity to loading.

Yarn-like carbon nanotube (CNT) fibres are a hierarchically-structured material with a variety of promising applications such as high performance composites, sensors and actuators, smart textiles, and energy storage and transmission. However, in order to fully realize these possibilities, a more detailed understanding of their interactions with the environment is required. In this work, we describe a simplified representation of the hierarchical structure of the fibres from which several mathematical models are constructed to explain electro-structural interactions of fibres with organic liquids. A balance between the elastic and surface energies of the CNT bundle network in different media allows the determination of the maximum lengths that open junctions can sustain before collapsing to minimize the surface energy. This characteristic length correlates well with the increase of fibre resistance upon immersion in organic liquids. We also study the effect of charge accumulation in open interbundle junctions and derive expressions to describe experimental data on the non-ohmic electrical behaviour of fibres immersed in polar liquids. Our analyses suggest that the non-ohmic behaviour is caused by progressively shorter junctions collapsing as the voltage is increased. Since our models are not based on any property unique to carbon nanotubes, they should also be useful to describe other hierarchical structures.

We report a previously unseen non-ohmic effect in which the resistivity of carbon nanotube fibers immersed in polar liquids is modulated by the applied electric field. This behavior depends on the surface energy, dielectric constant, and viscosity of the immersion media. Supported by synchrotron SAXS and impedance spectroscopy, we propose a model in which the gap distance, and thus the conductance, of capacitive interbundle junctions is controlled by the applied field.

The organisation of poly-glucan chains into cellulose macromolecular microfibrils has been studied using small angle X-ray scattering (SAXS). Three kinds of cellulose - bacterial cellulose (BC), nata-de-coco (NdC) (food grade bacterial cellulose) and tunicate cellulose (TC) have been investigated. Given the large ambiguity in literature on the microfibril dimensions owing to different methods and data analysis strategies, a method to extract dimensions of cellulose microfibrils using SAXS has been shown, which was found to be consistent across all the samples. The results have been verified with microscopy data. Two populations of microfibrils with different cross-section dimensions were identified. The dimensions of the rectangular cross-sections of BC were found to be 32nm by 16nm and 21nm by 10nm. The dimensions for NdC were calculated to be 25nm×8nm and 14nm×6nm and that for TC were determined to be 25nm×10nm and 15nm×8nm., (Copyright © 2014 Elsevier B.V. All rights reserved.)

The CVD process for the spinning of carbon nanotube (CNT) fibres combines the nucleation, growth and aggregation of CNTs in the form of an aerogel with fibre spinning into a single process step. The optimisation of the process requires agility in multi-dimensional parameter space, so one tends to find parameter 'islands' where spinning is possible, while exploration tends to follow 'routes' through this space. Here, we follow two such routes, one of which drastically improves fibre purity, the other changes the nature of the nanotubes comprising the fibres from multiwall to single wall. In the first case there is only a modest enhancement of the mechanical properties, but in the second a very considerable improvement is seen. In terms of the conditions required to make fibres comprising predominately single wall CNTs, the key factor appears to be the rigorous control of the sulphur addition, in trace quantities, coupled with the availability of carbon atoms at the earliest stage after injection, typically in the range 400-500 °C. A model is presented for the role of sulphur in floating catalysts CNT synthesis.

Carbon nanotube (CNT) fibers consist of a network of highly oriented carbon nanotube bundles. This paper explores the ingress of liquids into the contiguous internal pores between the bundles using measurements of contact angles and changes in fiber dimensions. The resultant effects on the internal structure of the fiber have been examined by WAXS and SAXS. A series of time-resolved experiments measured the influence of the structural changes on the electrical resistivity of the fiber. All organic liquids tested rapidly wicked into the fiber to fill its internal void structure. The local regions in which the nanotube bundles are aggregated to give a bundle network were broken up by the liquid ingress. For the range of organic penetrants examined, the strength of the effects on structure and electrical resistivity was correlated, not only with the degree to which the liquid reduced the nanotube surface energy, but also with the Hansen affinity parameters. The fact that liquid environments influence the electrical performance of these fibers is of significance if they are to replace copper as power and signal conductors, with added implications regarding the possible ingress of external insulating materials, and possibly also sensing applications.

The ability to simply and economically produce carbon nanotubes (CNTs) with a defined chiral angle is crucial for the exploitation of nanotubes for their electrical properties. We investigate a diverse range of nitrogen sources for their ability to control CNT chiral angle via epitaxial growth from highly ordered catalyst particles. Through the use of in situ mass and infrared spectrometry, we elucidate the mechanism by which these ordered catalyst particles are formed, showing that ammonia is a key intermediate in the process. Subsequently, the direct addition of a small amount of ammonia to an otherwise standard CNT synthesis is shown to be able to form catalyst particles that grow single chiral angle multiwalled carbon nanotubes. Variation in the ammonia concentration clarifies the catalyst restructuring necessary for the epitaxial growth of carbon nanotubes and subsequent chiral angle control. The simple addition of a nitrogen source is an attractive route for chiral angle control; however, the model also suggests further ways to optimize CNT chiral angle distributions as well as to improve CNT and graphene yield and crystallinity. This understanding also explains the action of ammonia in its widely used role in activating catalyst prior to CNT growth. Finally, this work highlights the uses of novel surface geometries that are achievable through multiphase catalysts.

Translating the remarkable mechanical properties of individual carbon nanotubes to macroscopic assemblies presents a unique challenge in maximizing the potential of these remarkable entities for new materials. Infinitely long individual nanotubes would represent the ideal molecular building blocks; however, in the case of length-limited nanotubes, typically in the range of micro- and millimeters, an alternative strategy could be based on the improvement of the mechanical coherency between bundles assembling the macroscopic materials, like fibers or films. Here, we present a method to enhance the mechanical performance of fibers continuously spun from a CVD reactor, by a postproduction processing methodology utilizing a chemical agent aided by UV irradiation. The treatment results in an increase of 100% in specific strength and 300% in toughness of the fibers with strength values rocketing to as high as 3.5 GPa SG(-1). An attempt has been made to explore the nature of the chemical modifications introduced in the fiber and the consequential effects on its properties.

A commercial thermoplastic polyurethane is identified for which the addition of nanotubes dramatically improves its mechanical properties. Increasing the nanotube content from 0% to 40% results in an increase in modulus, Y, (0.4-2.2 GPa) and stress at 3% strain, σ(ϵ = 3%) , (10-50 MPa), no significant change in ultimate tensile strength, σ(B) , (≈50 MPa) and decreases in strain at break, ϵ(B) , (555-3%) and toughness, T, (177-1 MJ m(-3) ). This variation in properties spans the range from compliant and ductile, like an elastomer, at low mass fractions to stiff and brittle, like a rigid thermoplastic, at high nanotube content. For mid-range nanotube contents (≈15%) the material behaves like a rigid thermoplastic with large ductility: Y = 1.5 GPa, σ(ϵ = 3%) = 36 MPa, σ(B) = 55 MPa, ϵ(B) = 100% and T = 50 MJ m(-3) . Analysis suggests that soft polyurethane segments are immobilized by adsorption onto the nanotubes, resulting in large changes in mechanical properties., (Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

A model for the strength of pure carbon nanotube (CNT) fibers is derived and parametrized using experimental data and computational simulations. The model points to the parameters of the subunits that must be optimized in order to produce improvements in the strength of the macroscopic CNT fiber, primarily nanotube length and shear strength between CNTs. Fractography analysis of the CNT fibers reveals a fibrous fracture surface and indicates that fiber strength originates from resistance to nanotube pull-out and is thus proportional to the nanotube-nanotube interface contact area and shear strength. The contact area between adjacent nanotubes is determined by their degree of polygonization or collapse, which in turn depends on their diameter and number of layers. We show that larger diameter tubes with fewer walls have a greater degree of contact, as determined by continuum elasticity theory, molecular mechanics, and image analysis of transmission electron micrographs. According to our model, the axial stress in the CNTs is built up by stress transfer between adjacent CNTs through shear and is thus proportional to CNT length, as supported by data in the literature for CNT fibers produced by different methods and research groups. Our CNT fibers have a yarn-like structure in that rather than being solid, they are made of a network of filament subunits. Indeed, the model is consistent with those developed for conventional yarn-like fibers.

We have prepared polyvinylalcohol-SWNT fibers with diameters from ∼1 to 15 μm by coagulation spinning. When normalized to nanotube volume fraction, V(f), both fiber modulus, Y, and strength, σ(B), scale strongly with fiber diameter, D: Y/V(f) ∝ D(-1.55) and σ(B)/V(f) ∝ D(-1.75). We show that much of this dependence is attributable to correlation between V(f) and D due to details of the spinning process: V(f) ∝ D(0.93). However, by carrying out Weibull failure analysis and measuring the orientation distribution of the nanotubes, we show that the rest of the diameter dependence is due to a combination of defect and orientation effects. For a given nanotube volume fraction, the fiber strength scales as σ(B) ∝ D(-0.29)D(-0.64), with the first and second terms representing the defect and orientation contributions, respectively. The orientation term is present and dominates for fibers of diameter between 4 and 50 μm. By preparing fibers with low diameter (1-2 μm), we have obtained mean mechanical properties as high as Y = 244 GPa and σ(B) = 2.9 GPa.

This work shows a simple, single-stage, scalable method for the continuous production of high-quality carbon nanotube-polymer transparent conductive films from carbon feedstock. Besides the ease of scalability, a particular advantage of this process is that the concentration of nanotubes in the films, and thus transparency and conductivity, can be adjusted by changing simple process parameters. Therefore, films can be readily prepared for any application desired, ranging from solar cells to flat panel displays. Our best results show a surface resistivity of the order of 300 Ω square -1 for a film with 80% transparency, which is promising at this early stage of process development.

Hydroxyapatite-carbon nanotube (HA-CNT) composites have the potential for improved mechanical properties over HA for use in bone graft applications. Finding an appropriate sintering atmosphere for this composite presents a dilemma, as HA requires water in the sintering atmosphere to remain phase pure and well hydroxylated, yet CNTs oxidize at the high temperatures required for sintering. The purpose of this study was to optimize the atmosphere for sintering these composites. While the reaction between carbon and water to form carbon monoxide and hydrogen at high temperatures (known as the 'water-gas reaction') would seem to present a problem for sintering these composites, Le Chatelier's principle suggests this reaction can be suppressed by increasing the concentration of carbon monoxide and hydrogen relative to the concentration of carbon and water, so as to retain the CNTs and keep the HA's structure intact. Eight sintering atmospheres were investigated, including standard atmospheres (such as air and wet Ar), as well as atmospheres based on the water-gas reaction. It was found that sintering in an atmosphere of carbon monoxide and hydrogen, with a small amount of water added, resulted in an optimal combination of phase purity, hydroxylation, CNT retention and density.

Reactive oxygen species (ROS) production is important in the toxicity of pathogenic particles such as fibres. We examined the oxidative potential of straight (50 microm and 10 microm) and tangled carbon nanotubes in a cell free assay, in vitro and in vivo using different dispersants. The cell free oxidative potential of tangled nanotubes was higher than for the straight fibres. In cultured macrophages tangled tubes exhibited significantly more ROS at 30 min, while straight tubes increased ROS at 4 h. ROS was significantly higher in bronchoalveolar lavage cells of animals instilled with tangled and 10 mum straight fibres, whereas the number of neutrophils increased only in animals treated with the long tubes. Addition of dispersants in the suspension media lead to enhanced ROS detection by entangled tubes in the cell-free system. Tangled fibres generated more ROS in a cell-free system and in cultured cells, while straight fibres generated a slower but more prolonged effect in animals.

The aggregation of two de novo designed surfactant-like peptides, with sequences Ac-IIKKEENN-OH (P1) and Ac-IIEENNDD-OH (P2), has been studied in aqueous solution at various pH values using titration, Circular dichroism (CD), Fourier transform infrared spectroscopy (FTIR), and atomic force microscopy (AFM). It was found that aggregates of P1 and P2 both display 5 pK(a)'s, some of which differ considerably from the tabulated values for those amino acids. In particular, a lysine of P1 titrated to 4.939 +/- 0.066. CD spectra of P1 were insensitive to pH, while CD spectra of P2 demonstrated a random coil-to-beta-sheet transition as pH was decreased. AFM images confirmed that P1 aggregates were spheres at all pH values and ranged in size from 3 to 20 nm. On the other hand, P2 aggregates were twisted ribbons below pH 4 but spheres less than 10 nm above pH 4. In addition, AFM images demonstrated the partial breakup of these twisted ribbons upon elevating the pH from 3.03 to 3.46 and the virtual disappearance of ribbons at pH 3.82. FTIR spectra of P2 indicate a structural transition from random coil to beta-sheet as pH was decreased. The role of backbone hydrogen bonding as well as charge is discussed.

We report on a series of experiments on the aqueous, nematic liquid crystalline phase of single-wall carbon nanotubes (SWNTs) and their ordered assemblies on the solid substrates. The nanotubes were dispersed at a low concentration of isotropic phase, and the concentration was gradually increased by the controlled evaporation of water. In-situ isotropic-to-liquid crystalline phase transition via a biphasic region was observed during water evaporation. Drying on a substrate demonstrated the effect of surface fields on the order and alignment of SWNTs in the liquid suspension and the influence on the structure of the deposited nanotubes after evaporation.

We report studies of the orientation state of multiwalled carbon nanotubes (MWNTs) dispersions in steady and transient shear flows. Uncured epoxy was used as a viscous Newtonian suspending medium and samples were prepared from "aligned" MWNTs using methods previously reported [S. S. Rahatekar et al., J. Rheol. 50, 599 (2006)]. Orientation measurements were performed in both the flow-gradient (1-2) and flow-vorticity (1-3) plane of simple shear flow using in situ x-ray scattering techniques. Steady state measurements in the 1-2 plane indicate that the MWNT orientation is shear rate dependent, with the MWNTs orienting closer to the flow direction at higher shear rates. During steady shear, anisotropy was measured to be higher in the 1-2 plane than in the 1-3 plane, demonstrating that the nanotube orientation state is not unaxially symmetric in shear. It is hypothesized that the steady state MWNT orientation is governed primarily by a rate-dependent state of nanotube aggregation/disaggregation, which was separately characterized by optical microscopy of the same samples under shear. High flux synchrotron radiation allowed for time-resolved structural studies in transient flows. A partial relaxation of flow-induced anisotropy was observed following flow cessation, despite the very small rotational diffusivity estimated for these nanotubes. Long transients are observed in step-down experiments, as the orientation state changes in response to the slow tube aggregation process.

In this work we report on the photo-catalytic performance of phase-pure and iron-doped anatase and rutile nanotubes, produced via a sol-gel process using pristine carbon nanotubes as templates. The encapsulated iron residues can be used to in situ dope the TiO(2) nanotubes without phase separation. The anatase and rutile nanotubes were further impregnated with platinum crystals with a uniform dispersion and an average size of approximately 2 nm. The materials showed dramatically improved activities for the photo-catalytic splitting of water compared to commercial TiO(2) with similar surface area (up to two orders of magnitudes), due to their higher illumination area, extended absorption range and reduced electron-hole recombination rate. The homogeneous dispersion of platinum nanoparticles further increased the hydrogen evolution rate for anatase nanotubes by a factor of seven in comparison to that for the pristine material, thus proving the great potential for commercial applications.

A simple process to spin fibers consisting of multi-walled carbon nanotubes (CNTs) directly from their lyotropic liquid-crystalline phase is reported. Ethylene glycol is used as the lyotropic solvent, enabling a wider range of CNT types to be spun than previously. Fibers spun with CNTs and nitrogen-doped CNTs are compared. X-ray analysis reveals that nitrogen-doped CNTs have a misalignment of only +/-7.8 degrees to the fiber axis. The tensile strength of the CNT and nitrogen-doped CNT fibers is comparable but the modulus and electrical conductivity of the are lower. The electrical conductivity of both types of CNT fibers is found to be highly anisotropic. The results are discussed in context of the microstructure of the CNTs and fibers.

Sulphur has been recognised as a growth promoter for carbon fibres and carbon nanotubes for over 30 years. Moreover, the Fe-C-S system, in particular, has been extensively studied for more than half a century in the fields of steelmaking and cast iron. In the present work we examine the role of sulphur in the iron-catalysed growth of carbon nanotubes during the process of direct spinning of fibres from the gas phase. A detailed microstructural characterisation of the reaction products was conducted by high resolution TEM and EELS composition mapping on a dedicated FEG STEM (VG HB 501) equipped with Cs aberration correctors. Our results agree with previous works in classical metallurgy, indicating that sulphur forms a layer on the surface of the catalyst particles that plays a role in encouraging nanotube growth by surface diffusion.

Exceptionally long C60 nanowires, with a length to width aspect ratio as large as 3000, are grown from a 1,2,4-trimethylbenzene solution of C60. They have been formed to possess a highly unusual morphology, with each nanowire being composed of two nanobelts joined along the growth direction to give a V-shaped cross section. The crystal structure of these nanowires is found to be orthorhombic, with the unit cell dimensions of a = 10.2 A, b = 20.5 A, and c = 25.6 A. Structural and compositional analyses enable us to explain the observed geometry with an anisotropic molecular packing mechanism that has not been observed previously in C60 crystal studies. The nanowires have been observed to be able to transform into carbon nanofibers following high-temperature treatment, but the original V-shaped morphology can be kept unchanged in the transition. A model for the nanowire morphology based upon the solvent-C60 interactions and preferential growth directions is proposed, and potentially it could be extended for use to grow different types of fullerene nanowires.

This paper considers the feasibility of replacing indium tin oxide (ITO) with spin-coated, polymer-based composite films that are filled with multiwalled carbon nanotubes (MWNTs). The coating mixture consists of a solvent with low volatility, a dissolved thermoplastic polymer, and MWNTs. The high aspect ratio of MWNTs and their good electrical conductivity enable electrical percolation at very low concentrations, so that films can be prepared that conduct electricity while retaining good optical transparency. Although the MWNTs are driven to aggregate by Van der Waals interactions, the high viscosity of the polymer/solvent solution enables the preparation of metastable, homogeneous dispersions. However, exposing the mixtures to shear leads to aggregation, the magnitude of which depends on the duration of the shear. This effect could be observed directly in spin-coated films using both optical microscopy and conductivity measurements, with aggregation causing a drop in conductivity at high nanotube loading, and more complex non-monotonic behavior at concentrations approaching the percolation threshold.

Here, we report a simple and efficient way for organizing carbon nanotubes, in particular, single-wall carbon nanotubes (SWNTs) into ordered structures from their dilute solutions. It was found that drying a droplet of carbon nanotube solution at room temperature on a wettable surface such as glass or silica wafer led to redistribution, accumulation, and organization of carbon nanotubes along the perimeter of the droplet. Unlike the aggregation behaviors of colloid nanoparticles, anistropic carbon nanotubes tended to show two orientations in a ring deposit: one parallel to the outer perimeter of the ring and the other normal to it in the interior. Drying droplets of SWNT solutions at high temperatures exhibited a long-range ordered structure. In addition, droplet drying may cause size separation of carbon nanotubes and pattern formation through interactions between droplets. This result helps us not only to further understand fluid dynamics during the drying process but also to provide a promising and simple strategy for either assembling carbon nanotubes on a surface or organizing them into well-aligned films and fibers.

Multi-walled carbon nanotubes were synthesized by chemical vapor deposition from pure toluene and toluene/diazine mixtures using ferrocene as a catalyst precursor at 760 degrees C. As recently announced, characterization of the resulting nanotube films showed that, unlike pure carbon nanotubes, those grown in the presence of nitrogen have an extremely high degree of internal order, both in terms of the uniform chirality in the nanotube walls and of the crystallographic register between them. Here, the structure, defects, and morphology of the nanotubes were analyzed in depth using advanced electron microscopy techniques, and compared with existing models and observations. Nitrogen, which seems to be responsible for the dramatic structural order, was found to segregate preferentially within the core of the nanotubes.

We present a novel method to produce pure rutile nanotubes using a sacrificial carbon nanotube template.

There is considerable interest in the adhesion of polymers to carbon nanotubes for nanocomposite applications.(1-4) One example is multiwalled carbon nanotubes (MWCNTs) dispersed in nylon 6,6.(5) We will show that high-contrast tomographic reconstructions can be created from plasmon-loss electrons that show the three-dimensional structural complexity of the MWCNT-nylon composite at the nanoscale. Further, by recording a series of energy-loss images at successive tilts, it is possible to interrogate subvolumes to extract energy-loss spectra from the reconstructed "volume spectra".

We describe a simple method for separating carbon nanotubes on the basis of their mesogenicity by fractionating biphasic aqueous suspensions within the Flory chimney of the lyotropic phase diagram. Macroscopic phase separation occurs on centrifuging the biphasic nanotube suspension or allowing it to stand. Long, straight nanotubes with higher mesogenicity (liquid crystalline forming ability) segregate preferentially to the liquid crystalline phase, whereas shorter nanotubes and impurities with lower mesogenicity segregate preferentially to the isotropic phase.

In this work, disclination interaction behavior in relation to Frank elastic constant anisotropy in nematics has been studied. A large number of (+(1/2), -(1/2)) disclination pairs are revealed by spontaneous band texture in a semiflexible copolyester. The pairs show no preferential relative orientation, with the intervening fields showing intermediate patterns. A two-dimensional tensor lattice model considering unequal elastic constants is applied to simulate the interaction behavior and patterns of disclination pairs in the presence of elastic anisotropy. Scaling laws for disclination density rho(t) as a function of time step t with different elastic anisotropy are obtained as t(-nu). The value of the exponent nu decreases as elastic anisotropy is increased. Obviously, elastic anisotropy slows the texture coarsening. The simulations also show that angular forces arise in the presence of elastic anisotropy and change the patterns of pairs during the texture coarsening. When disclination density is considerably decreased, some +(1/2) disclinations start to rotate to the energetically favored patterns depending on the sign of the elastic anisotropy. As a result of the disclination rotation, the distribution of patterns of pairs continues to change during the annihilation. However, disclination pairs are influenced not only by elastic anisotropy but also by disclination interaction during the whole annihilation. Therefore, in a real system, the dependence of pairs on elastic anisotropy is not as strong as the theoretical prediction for an isolated pair, and the full pattern range of disclination pairs can be observed.

A new route for the highly convenient scalable production of carbon nanofibers on a sodium chloride support has been developed. Since the support is nontoxic and soluble in water, it can be easily removed without damage to the nanofibers and the environment. Nanofiber yields of up to 6500 wt % relative to the nickel catalyst have been achieved in a growth time of 15 min. Electron microscopy (SEM, TEM) and thermal gravimetric analysis (TGA) indicated that the catalytically grown carbon had relatively little thermal over-growth and possessed either a herringbone or a semi-ordered nanostructure, depending on the growth conditions.

Single-walled carbon nanotubes (SWNTs) have been effectively wetted and dispersed in saturated sodium hydroxide (NaOH) alcohol-water solutions with little surface damage or shortening of the tubes; the treated material was dissolvable as individual tubes in many common organic solvents.

Many routes have been developed for the synthesis of carbon nanotubes, but their assembly into continuous fibers has been achieved only through postprocessing methods. We spun fibers and ribbons of carbon nanotubes directly from the chemical vapor deposition (CVD) synthesis zone of a furnace using a liquid source of carbon and an iron nanocatalyst. This process was realized through the appropriate choice of reactants, control of the reaction conditions, and continuous withdrawal of the product with a rotating spindle used in various geometries. This direct spinning from a CVD reaction zone is extendable to other types of fiber and to the spin coating of rotating objects in general.

We present classical molecular dynamics simulations demonstrating that single-wall carbon nanotube (SWNT) bundles collapse under hydrostatic pressure. The collapse pressures obtained as a function of nanotube diameter are in excellent quantitative agreement with new data presented here for small diameter (d approximately 0.8 nm) SWNTs, and the majority of previously published results, although there remain some unreconciled contradictions in the literature. The collapse pressure is found to be independent of the nanotube chirality, and a lower limit on the largest SWNT that remains inflated at atmospheric pressure is established (d>4.16 nm).

A simple method for the synthesis of high purity single wall carbon nanotubes has been developed by using nickel formate as a precursor for the formation of nearly mono-dispersed nickel seed-nanoparticles as catalysts in the CVD growth process.

Neurodegenerative diseases resulting from expanded repeat sequences of glutamine residues are associated with the formation of protein aggregates in the cell nuclei of the affected neurons, but whether these are pathogenic is controversial. Recent observations indicate that the ages of onset of these diseases are exponential functions of the repeat lengths and that the probability of neural death is constant with time. The only process known to us that could give rise to such behaviour is nucleation of the aggregates.

In this paper, a deterministic model, which considers the three Frank elastic constants, is introduced. It is based on a lattice model and a director is used to represent the orientation of the liquid crystals in each cell. A tensor expression of the so-called "texture field" is deduced so that the nematic symmetry is conserved automatically. In the current model, the evolution of the director field can be viewed as a process towards the state of zero elastic torque. The model forms the basis for an improved understanding of the mesoscale structures and rheological phenomena of nematic liquid-crystalline polymers. It has been tested in its ability to reproduce the Fréedericksz transitions, and simulations of thin liquid crystalline polymer films clearly show the effect of unequal elastic constants on the director microstructure evolution.