Mesoporous materials with pore diameters in the range 2–50 nm forming tubular or fibrous structures are of great interest due to their unique properties. Because they are commonly used as sorbents and catalyst carriers, knowledge of their surface area and porosity is critical. A modified intercalation/deintercalation method was used to increase the efficiency of nanotube formation from kaolin-group minerals which differ in terms of their degree of structural order. Unlike previous experiments, in the procedure adopted in the present study, methanol was used instead of 1,3-butanediol for grafting reactions and octadecylamine intercalation was also performed. The samples were examined using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), and transmission electron microscopy (TEM). The specific surface area and porosity of previously described and newly formed materials were investigated by N2 adsorption/desorption. Compared to results described earlier, the percent yield of nanotubes obtained in the present study was significantly greater only in the case of ‘Maria III’ kaolinite, which has high structural order. This increase was obtained mainly by the grafting reaction with methanol. Highly ordered stacking of kaolinite-methanol intercalates was noticed and, thus, the amine intercalation was more efficient. In particular, the use of long-chain octadecylamine significantly increased the nanotube yield. The grafting reaction with methanol procedure yielded fewer nanotubes, however, when applied to poorly ordered samples (‘Jaroszów’ kaolinite and ‘Dunino’ halloysite). In the case of the ‘Maria III’ kaolinite, the diameter of the rolled layers observed by TEM was ~30 nm and corresponded to average diameters of newly formed pores (DmN) determined using N2 adsorption/desorption, confirming that nanotubes contributed to an increase in surface area and total pore volume. In the case of ‘Jaroszów’ kaolinite and ‘Dunino’ halloysite mainly macropores (DmN > 100 nm) and mesopores (20 nm > DmN > 40 nm) were formed. The pores were attributed to interparticle and interaggregate spaces in the stacks of platy particles and to the small relative number of nanotubes.

Kaolin-group clay minerals can be modified to form nanotubular and mesoporous structures with interesting catalytic properties, but knowledge of the best methods for preparing these structures is still incomplete. The objective of this study was to investigate intercalation/deintercalation as a method for the delamination and rolling of kaolinite layers in relation to structural order. To prepare nanotubular material, kaolinites of different crystallinities and halloysite (all from Polish deposits) were chosen. The experimental procedure consisted of four stages: (1) preparation of a dimethyl sulfoxide precursor intercalate; (2) interlayer grafting with 1,3-butanediol; (3) hexylamine intercalation; and (4) deintercalation of amine-intercalated minerals using toluene as the solvent. Structural perturbations and changes in the morphology of the minerals were examined by X-ray diffraction, Fourier transform infrared spectroscopy, differential scanning calorimetry, and transmission electron microscopy (TEM). The number of rolled kaolinite layers depended heavily on the efficiency of the intercalation steps. An increase in the structural disorder and extensive delamination of the minerals subjected to chemical treatment were recorded. Kaolinite particles which exhibited tubular morphology or showed rolling effects were observed using TEM. The nanotubes formed were ∼30 nm in diameter, with their length depending on the particle sizes of the minerals.

Halloysite nanotubes (HNTs) are hollow clay nanotubes in the nanometer size range, made up of double-layered aluminum silicate mineral layers. HNTs represent an extremely versatile, safe, and biocompatible nanomaterial, used in a wide range of applications in biomedicine and nanomedicine. For example, they are used as transporters for the controlled release of drugs or genes, in tissue engineering, in the isolation of stem cells and cancer cells, and in bioimaging. Consequently, the assessment of the biocompatibility of HNTs has acquired considerable importance. In recent years, HNT composites have attracted attention due to their improved biocompatibility, compared to HNTs, suggesting potential for applications in tissue engineering or as vehicles for drugs or genes. In this review, recent advances in the application of HNTs and HNT composites in biomedicine are discussed to provide a valuable guide to scientists in the design and development of viable, functional bio-devices for biomedical applications.

Understanding the physical structure of greases can provide critical insight into improving the lubricating performance of a grease. Observation of the grease structure can be quite difficult depending on the type of grease and the length scale of the structure. Polyurea greases in previous reports have typically been examined by removal of the oil phase, which significantly changes the polyurea structure. This paper examines the effect of sample preparation conditions on the microstructure of polyurea greases. This study reveals new structures in the polyurea that have not been observed in the previous literature, including entangled fibers and nanotubes. Correlation is found between the observed polyurea microstructure coverage and grease stiffness.

Kaolinite was intercalated with n-hexylamine, n-octadecylamine and n-docosanamine, using methanol-kaolinite as the precursor. The intercalation compound with n-docosanamine presented the largest basal spacing for a kaolinite derivative thus far reported (64.2 Å). Five grafted derivatives of kaolinite were directly intercalated with n-hexyl- and n-octadecylamine. During intercalation, the grafted molecules rearrange from parallel to perpendicular orientation to the kaolinite surface, in order to maximize the interaction with the amine and minimize the interlayer expansion needed. The octadecylamine intercalation compounds were delaminated in toluene, accompanied by the deintercalation of the amine molecules. Thin kaolinite particles rolled into a halloysite-like morphology, but forming much smaller tubes, some of which possibly consist of single kaolinite layers. The delamination was more efficient with the grafted kaolinites than with raw kaolinite.

Twenty one samples of relatively pure tubular halloysites (HNTs) from localities in Australia, China, New Zealand, Scotland, Turkey and the USA have been investigated by X-ray diffraction (XRD), infrared spectroscopy (IR) and electron microscopy. The halloysites occur in cylindrical tubular forms with circular or elliptical cross sections and curved layers and also as prismatic tubular forms with polygonal cross sections and flat faces. Measurements of particle size indicate a range from 40 to 12,700 nm for tube lengths and from 20 to 600 nm for diameters. Size distributions are positively skewed with mean lengths ranging from 170 to 950 nm and mean diameters from 50 to 160 nm. Cylindrical tubes are systematically smaller than prismatic ones. Features related to order/ disorder in XRD patterns e.g. as measured by a ‘cylindrical/prismatic’ (CP) index and IR spectra as measured by an ‘OH-stretching band ratio’ are related to the proportions of cylindrical vs. prismatic tubes and correlated with other physical measurements such as specific surface area and cation exchange capacity. The relationships of size to geometric form, along with evidence for the existence of the prismatic form in the hydrated state and the same 2M1 stacking sequence irrespective of hydration state (i.e. 10 vs. 7 Å) or form, suggests that prismatic halloysites are the result of continued growth of cylindrical forms.

A test of the qualities of polarizing filters was performed for a set of specimens including a bulk Nicol prism, standard polaroids, and special polyvinyl alcohol (PVA)-iodine thin-film filters coated on both sides by vertically oriented carbon nanotubes. The residual transmission of polarizing filters depending on the incidence angle of polarized light was examined in detail. The superior quality of polarizing film filters treated with carbon nanotubes was found. This fact allows us to propose a new application for polarizing films with carbon nanotubes for a polarizing cover glass. In such a way the cover glass may serve as an analyzer in a light polarizing microscope. Some features of optical scheme arrangement for the polarizing technique are discussed. The polarizing cover glass allows elimination of depolarization of light, which is inserted in a microscope objective. Test results of the proposed polarizing technique attest to the efficiency of using the polarizing cover glass. The new scheme for polaroid arrangement shows image-contrast enhancement by several percent in comparison with the standard layout.

The aim of this research study is to produce high-quality TiO2 nanotube arrays using porous alumina templates. The templates are fabricated through anodizing bulk aluminum foils which can be utilized for the production of thick alumina templates. To produce the nanotube arrays, the alumina template pores are filled with the precursor sol by applying a DC electric field. Then, the deposited nanotubes are heat treated at 320 °C for 2 h and, subsequently, sintered for 2 h at 400 and 750 °C to obtain nanotubes with pure anatase and rutile phases, respectively, as confirmed by x-ray diffraction data. Scanning and transmission electron microscopy (SEM and TEM) investigations show that the nanotubes have been deposited in the channels of the nanoporous alumina template. Also, SEM investigations show the existence of a vast area of TiO2 nanotube arrays when we use semiconductor alumina templates.

Use of nanostructured TiO2 for photocatalysis is a cost-effective and sustainable technology. However, to make this an attractive viable technology will require the design of TiO2 photocatalyst capable of harnessing the energy of visible light. One possible solution is the doping of TiO2 to reduce its band gap. In this paper, the effect of Cr-doping by ion implantation on the in situ crystallization and phase stability of anodic TiO2 nanotubes at elevated temperature is described. Cr-doping has dramatically reduced the fraction of anatase-to-rutile transformation and lowered the crystallization temperature of anatase from 600 to 400 °C and rutile from 600 to 500 °C. Ion beam analysis by Rutherford backscattering spectrometry has confirmed the existence of Cr ions composition gradation in doped TiO2 nanotubes. The real doping of Ti lattices with Cr ions was evidenced by the analyses of surface compositions and chemical states of the nanotubes using x-ray photoelectron spectroscopy.

We consider the zigzag half-nanotubes (tight-binding approximation) in a uniform magneticfield which is described by the magnetic Schrödinger operator with a periodic potentialplus a finitely supported perturbation. We describe all eigenvalues and resonances of thisoperator, and theirs dependence on the magnetic field. The proof is reduced to theanalysis of the periodic Jacobi operators on the half-line with finitely supportedperturbations.

The hyper-Wiener index of a connected graph G is defined as , where V (G) is the set of all vertices of G and d(u,v) is the distance between the vertices u,v∈V (G). In this paper we find an exact expression for the hyper-Wiener index of TUHC6[2p,q], the zigzag polyhex nanotube.

Electromagnetic response of individual boron nitride nanotubes (BNNTs) has been studied by spatially resolved electron energy loss spectroscopy (EELS). We demonstrate how dedicated EELS methods using subnanometer electron probes permit the analysis of local dielectric properties of a material on a nanometer scale. The continuum dielectric model has been used to analyze the low-loss EEL spectra recorded from these tubes. Using this model, we demonstrate the weak influence of the out-of-plane contribution to the dielectric response of BNNTs. The optical gap, which can be deduced from the measurements, is found to be equal to 5.8 ± 0.2 eV, which is close to that of the hexagonal boron nitride. This value is found to be independent of the nanotubes configuration (diameter, helicity, number of walls, and interaction between the different walls).

In this paper, we suggest the creation of a nanoparticles and nanotubes by using the interaction of a femtosecond laser with a solid target in a vacuum. A simple model is used to predict the optimal target and the laser parameters for the production of efficient nanoparticles. At the Soreq laboratory, experiments are performed with aluminium and carbon targets using a femtosecond laser. The irradiated targets are composed of either a thin layer of aluminium or of carbon, deposited on a transparent heat-insulating glass substrate. The nanoparticle debris is collected on a silicone wafer for X-ray diffraction (XRD), for scanning electron microscopy (SEM), and for atomic force microscopy (AFM). For transmission electron microscopy (TEM), the debris is caught on a copper grid covered on one side with a carbon membrane. Our experiments confirm the creation of crystal nanoparticles for aluminium and nanotubes for carbon experiments.

Numerous human diseases are associated with conformational change and aggregation of proteins, including Alzheimer's, Parkinson's, prion diseases (such as mad cow disease), familial amyotrophic lateral sclerosis (ALS, or Lou Gehrig's disease), Huntington's, and type II (mature onset) diabetes. In many cases, it has been demonstrated that conformational change and aggregation can occur outside living cells and complex biochemical networks. Hence, approaches from materials and physical science have enhanced our understanding of the role of protein aggregation in these diseases at the molecular and nanoscale levels. In this article, we will review what is known about these protein structures from the perspective of materials science, focusing on the details of emergent oligomeric and nanotube-like structures, their interactions with model lipid bilayers, how the structures relate to observed biological phenomena, and how protein aggregation and amyloid formation can be employed for the good in biology and materials science.

The Young's modulus of WS2 nanotubes is an important property for various applications. Measurements of the mechanical properties of individual nanotubes are challenged by their small size. In the current work, atomic force microscopy was used to determine the Young's modulus of an individual multiwall WS2 nanotube, which was mounted on a silicon cantilever. The buckling force was measured by pushing the nanotube against a mica surface. The average Young's modulus of an individual WS2 nanotube, which was calculated by using Euler's equation, was found to be 171 GPa. First-principle calculations of the Young's modulus of MoS2 single-wall nanotubes using density-functional–based tight-binding method resulted in a value (230 GPa) that is close to that of the bulk material. Furthermore, the diameter dependence of the Young's modulus in both zigzag and armchair configuration was studied and was found to approach the bulk value for nanotubes with few-nanometer diameters. Similar behavior is expected for WS2 nanotubes. The mechanical behavior of the WS2 nanotubes as atomic force microscope imaging tips gave further support for the measured Young's modulus.

Titania nanotubes synthesized by a soft chemical process are described, having diameters of 8 nm to 10 nm and lengths ranging from approximately 0.1 μm to 1 μm. X-ray diffraction studies show the structure of the as-prepared nanotubes is the same as that of the starting anatase TiO2 nanoparticles. Energy-dispersive x-ray analysis and electron energy loss spectroscopy studies further indicate that the as-prepared nanotubes are composed of titania. Studies using transmission electron microscopy verified that the nanotubes are formed during alkali treatment, with subsequent acidic treatments having no effect on nanotube structure and shape.

Nanotubular structures in the B-C-N ceramic system represent an intriguing alternative to conventional carbon nanotubes.Because of the ability to widely vary the chemical composition of nanotubes within the B-C-N ternary phase diagram and to change the stacking of C-rich or BN-rich tubular shells in multiwalled structures, a wide horizon opens up for tuning nanostructure electrical properties.Pure carbon nanotubes are metals or narrow-bandgap semiconductors, depending on the helicity and diameter, whereas those of BN are insulators with a ∼5.0eV gap independent of these parameters.Thus, the relative B/C/N ratios and/or BN-rich and C-rich domain spatial arrangements, rather than tube helicity and diameter, are assumed to primarily determine the B-C-N nanotube electrical response.This characteristic is highly valuable for nanotechnology:while tube diameter and helicity are currently difficult to control, continuous doping of C with BN, or vice versa, proceeds relatively easily due to the isostructural nature of layered C and BN materials.In this article, recent progress in the synthesis, microscopic analysis, and electrical property measurements of a variety of compound nanotubes in the ceramic B-C-N system is documented and discussed.

This article serves to introduce the January 2004 issue of MRS Bulletin on progress toward applications of ceramic nanostructures. Conventional ceramic materials are widely used today in areas ranging from structural to biological applications, and in devices as diverse as lasers, semiconductors, sensors, and piezoelectric components. Such materials include oxides, carbides, nitrides, mixed oxides, and composites.Over the last decade, the use of ceramic nanostructures has already changed the approach to materials design in many of these applications, by seeking structural control at the atomic level and tailoring of the engineering properties. The articles in this issue review the advantages of nanoceramics, their application in various fields, and the challenges involved in their fabrication.