Thermal conductivity of crystalline chrysotile asbestos

The thermal conductivity of crystalline chrysotile asbestos made up of hollow tubular Mg₃Si₂O₅(OH)₄ filaments is measured in the range 5–300 K. The paper discusses the possibility of using this material in studies of the thermal conductivity of thin filaments of metals and semiconductors incorporated into the channels of crystalline chrysotile asbestos tubes.     

Asbestos Particle Characteristics Important for the Filter Cake Formation

Two types of asbestos fiber, chrysotile and amosite, form filter cakes of different permeabilities while having a similar degree of dispersion. The filter cake resistance depends on the disperse phase characteristics and the conditions of cake formation. The main reason for the effects mentioned is different particle flexibility influenced by the specific structure of each type of asbestos particle. The flexible chrysotile fibers in the cake form dense and rigid, amosite, porous deposits. An increase in the velocity of the suspended chrysotile particles, caused by pressure difference and agitation, results in significant differences in filter cake resistance.     

Cylindrical GaAs quantum wires incorporated within chrysotile asbestos nanotubes: fabrication and polarized optical absorption spectra

GaAs has been injected into chrysotile asbestos channels. GaAs quantum wires (nanocylinders) with diameters ∼ 6 nm have been observed in the channels by means of transmittance electron microscopy. Polarized optical absorption spectra of asb-GaAs (chrysotile asbestos containing GaAs wires) have been studied. A high anisotropy of the absorption has been observed, and intersubband transitions in the visible light region due to a strong quantum size effect have been found.     

Investigation of longitudinal vibrations of -O-H groups in chrysotile asbestos by neutron scattering and polarized infrared spectroscopy

The specific features of the vibrational spectra of chrysotile asbestos, which is a natural mineral that represents a system of closely packed tubular fibers with an outer diameter of ∼30 nm, an inside diameter of ∼5 nm, and a length up to a centimeter and more, have been investigated using neutron scattering and polarized infrared spectroscopy. This material can serve as a natural matrix for the preparation of nanostructures by filling channels with various materials.     

Asbestos Analysis: A Review

Abstract

Prior to an asbestos removal the work requires first a substantiation, an identification, that asbestos is indeed present. This is known as a bulk analysis. Microscopical methods, particularly polarized light microscopy, can be used to measure the physical properties of fibers in the sampled material to identify and substantiate the presence of asbestos. Then, throughout the asbestos abatement process, the air is continuously monitored for asbestos fibers to minimize the risk exposure to the abatement worker as well as the general public. The measurement of air fiber levels throughout the abatement process is done primarily by phase contrast microscopy. When needed, electron microscopy is employed either in bulk asbestos analysis or the fiber in air measurements. In the USA, the usual methods that are followed are essentially prescribed. Laboratories and, under certain conditions the individual doing such work, should continuously meet performance criteria. The laboratory should be accredited and, for limited work, the individual certified. The overall procedure of asbestos analysis is reviewed; the possible current shortcoming in the methodology are discussed.     

A new approach to the decontamination of asbestos-polluted waters by treatment with oxalic acid under power ultrasound

A suspension of chrysotile asbestos fibres in aqueous 0.5M oxalic acid was subjected to power ultrasound with the aim to disrupt and detoxify the mineral by the leaching action of oxalic acid on its structural cations acting simultaneously with a vigorous acoustic cavitation. Sonication was performed in a "cavitating tube", a vertical hollow vibrating cylinder made of titanium, operating at 19.2 kHz and 150 W. Treatment lasted from 2.5 to 21 h. Scanning electron microscopy (SEM) showed that the joint action of the chelating agent and ultrasound (though not of either when applied independently) mostly converted asbestos fibres into micrometric aggregates and nano-sized debris, whose morphology totally differed from asbestos fibres. When treated suspensions were filtered through CA membranes (pore size 0.20 microm), more than half of the asbestos went through the filter because it had either been brought in solution or dispersed in the form of extremely small particles. Most of the structural metal ions were brought into solution (ICP-AES). After the treatment the BET surface area of the recovered solid was tenfold greater than the original. The crystalline fraction of residual solids, though resembling the original sample in XRD, was shown by micro-Raman spectra to be made of antigorite, a polymorph form of serpentine. Furthermore, as the length of these antigorite fibrils lay outside the fibre range rated as a health hazard under worldwide regulations, our procedure can be employed for the decontamination of chrysotile-polluted waters and sediments.     

Interphase characterization in polymer composites - monitoring of interphasial behavior in dependence on the mode of loading

Single fiber model composites consisting of epoxy resin matrix and differently sized glass fibers were investigated using pull-out tests, scanning electron microscopy (SEM), scanning force microscopy (SFM) and single fiber dynamic load test (SFDL). The inhomogeneous stress distribution along the embedded fiber length could be visualized by monitoring. SEM images showed either cohesive fracture or adhesive failure on pulled-out fibers with different sizings. The crack initiation and propagation were detected randomly and multiply distributed as the inhomogeneous interphase itself and depending strongly on the fiber-matrix model combination. The meniscus region acts as a material inhomogeneity and its appearence depends on the surface free energies of fiber and matrix and on the curing conditions of the resin. SFM in force modulation mode has visualized different interphase thicknesses and gradients of local stiffness. The SFDL test has been shown as a worthful tool for the comprehensive determination of fiber-matrix interaction.     

Optical properties of polymethine molecules incorporated into a macroscopic set of parallel nanotubes

The structural properties of polymethine molecules incorporated into nanofibers of chrysotile asbestos have been studied by absorption-spectroscopy methods. These experiments have shown that, in chrysotile nanotubes, monomeric, all-trans- and cis-isomers, dimers and J aggregates can be observed. Upon incorporation of a dye from weakly concentrated solutions, monomeric forms of polymethine molecules, extended chromophores of which are oriented along parallel asbestos nanotubes, are predominantly observed. The hybrid material under investigation may be of interest for applied problems.     

Capacity and thermal conductivity of a nanocomposite chrysolite asbestos-KDP (KH2PO4)

A nanocomposite chrysotile-KDP (KH₂PO₄) was prepared. KDP was introduced into empty nanochannels of chrysotile asbestos with diameters of ～5 nm. Thermal conductivity κ and heat capacity at a constant pressure C _p of the samples of chrysotile asbestos and nanocomposite chrysotile asbestos-KDP were measured in a temperature range of 80–300 K. Based on the analysis of the behavior of temperature dependences κ(T) and C _p (T) of the composite, temperatures of the ferroelectric transition T _F for KDP in nanochannels of chrysotile asbestos were determined. It turned out to be equal to ～250 K at T _F ～ 122 K for massive KDP samples.     

Comparative in vitro cytotoxicity assessment of some manufacturednanoparticulate materials characterized by transmissionelectron microscopy

A range of manufactured nanoparticulate materials, including Ag, TiO₂, Fe₂O₃, Al₂O₃, ZrO₂, Si₃N₄, and a range of carbonaceous nanoparticulate materials: single-wall and multi-wall carbon nanotube aggregates and aggregated nanoparticles of black carbon, as well as commercial (mineral grade) chrysotile asbestos nanotube aggregates, have been rigorously characterized by transmission electron microscopy. These nanoparticulate materials ranged in primary particle sizes from roughly 3 to 150 nm (except for the nanotube materials with lengths in excess of 15 μm). Aggregate sizes ranged from 25 nm to 20 μm. Comparative cytotoxicological assessment of these nanomaterials was performed utilizing a murine (lung) macrophage cell line. Considering the chrysotile asbestos to be a positive control, and assigning it a relative cytotoxicity index of unity (1.0), relative cytotoxicity indexes were observed as follows at concentrations of 5 μg/ml: 1.6 and ∼ 0.4 for Ag and TiO₂, respectively; 0.7–0.9 for the Fe₂O₃, Al₂O₃ and ZrO₂, 0.4 for the Si₃N₄, 0.8 for the black carbon, and 0.9 to 1.1 for the carbon nanotube aggregate samples. Observations of a cytotoxic response, nearly identical to that for chrysotile asbestos, for multi-wall carbon nanotube aggregates which very closely resemble anthropogenic multi-wall carbon nanotubes in the environment, raise some concern for potential health effects, especially for long-term exposure.     

表面增强拉曼光谱在食源性致病微生物检测中的应用研究

食源性致病微生物导致的食源性疾病已成为全球化的公共卫生问题。快速、有效地检测食源性致病微生物是实现食源性疾病预防与控制的关键环节，也是保障食品安全的技术关键。表面增强拉曼光谱(SERS)具有简单、快速、灵敏度高等优点，在食品安全、生物医学、环境监控等领域展现出良好的应用前景。介绍了近年来SERS在食源性致病微生物检测中的应用研究进展。对SERS技术概况、SERS增强理论及SERS增强基底进行了简要介绍，重点回顾了SERS在食源性致病微生物检测中的应用和发展现状。在食品安全分析方面，利用SERS与模式识别方法相结合对食品中常见食源性致病微生物能实现快速、有效鉴别，部分研究已应用于不同食品样品的分析，体现了SERS作为“指纹图谱”的分析优势；在医学诊断方面，SERS可对病理样品(如血液、尿液等)中食源性致病微生物进行快速检测，缩短了样本分析时间，使食源性疾病的快速诊断成为可能；随着微流控技术的发展，微流控平台结合SERS技术被称为“芯片实验室”应用于食源性致病微生物的检测，可提高分析的可控性，稳定性，特异性和灵敏度。通过对比分析，发现不同研究可采用不同分离方法、不同基底、不同目标捕获方式等实现了食源性致病微生物的检测，展示了不同方法间的差异性。已有研究表明了SERS在食源性致病微生物检测中应用可克服传统方法耗时等缺点，实现灵敏快速分析，为食品安全实时监控，食源性疾病即时诊断提供了有效的分析工具。同时，指出了SERS技术应用于食源性致病微生物分析依然面临很大挑战，(1)大多数研究并没有聚焦于实际样品，而标准培养液和实际样品的SERS检测存在较大差异，实际样品组分会对SERS响应产生干扰；(2)不同方法结果有较大差异，主要是由于纳米增强基底差异，吸附方式原理的差异，稳定性的差异等，因此需要更多深入研究进一步优化条件；(3)期望建立标准化的SERS方法替代传统技术，充分展示SERS作为新兴分析工具快速、灵敏、简捷的优势应用于食品安全，医学诊断等领域。将来，随着研究的深入及相关学科的发展，SERS作为极具潜力的快速分析工具，将在食品安全，生物医学等领域具有更广阔的应用前景。     

Comparative <Emphasis Type="Italic">in vitro</Emphasis> cytotoxicity assessment of some manufacturednanoparticulate materials characterized by transmissionelectron microscopy

A range of manufactured nanoparticulate materials, including Ag, TiO₂, Fe₂O₃, Al₂O₃, ZrO₂, Si₃N₄, and a range of carbonaceous nanoparticulate materials: single-wall and multi-wall carbon nanotube aggregates and aggregated nanoparticles of black carbon, as well as commercial (mineral grade) chrysotile asbestos nanotube aggregates, have been rigorously characterized by transmission electron microscopy. These nanoparticulate materials ranged in primary particle sizes from roughly 3 to 150 nm (except for the nanotube materials with lengths in excess of 15 μm). Aggregate sizes ranged from 25 nm to 20 μm. Comparative cytotoxicological assessment of these nanomaterials was performed utilizing a murine (lung) macrophage cell line. Considering the chrysotile asbestos to be a positive control, and assigning it a relative cytotoxicity index of unity (1.0), relative cytotoxicity indexes were observed as follows at concentrations of 5 μg/ml: 1.6 and ∼ 0.4 for Ag and TiO₂, respectively; 0.7–0.9 for the Fe₂O₃, Al₂O₃ and ZrO₂, 0.4 for the Si₃N₄, 0.8 for the black carbon, and 0.9 to 1.1 for the carbon nanotube aggregate samples. Observations of a cytotoxic response, nearly identical to that for chrysotile asbestos, for multi-wall carbon nanotube aggregates which very closely resemble anthropogenic multi-wall carbon nanotubes in the environment, raise some concern for potential health effects, especially for long-term exposure.This revised version was published online in August 2005 with a corrected issue number.     

Efficient field emission from coiled carbon nano/microfiber on copper substrate by dc-PECVD

Crystalline coiled carbon nano/micro fibers in thin film form have been synthesized via direct current plasma enhanced chemical vapor deposition (PECVD) on copper substrates with acetylene as a carbon precursor at 10 mbar pressure and 750 °C substrate temperature. The as-prepared samples were characterized by X-ray diffraction (XRD) analysis, scanning electron microscopy (SEM) and high resolution transmission electron microscopy (HRTEM). XRD pattern as well as selected area electron diffraction (SAED) pattern showed that the samples were crystalline in nature. SEM and HRTEM studies showed that as synthesized coiled carbon fibers are having average diameter ∼100 nm and are several micrometers in length. The as-prepared samples showed moderately good electron field emission properties with a turn-on field as low as 1.96 V/μm for an inter-electrode distance 220 μm. The variation of field emission properties with inter-electrode distance has been studied in detail. The field emission properties of the coiled carbon fibrous thin films are compared with that of crystalline multiwalled carbon nanotubes and other carbon nanostructures.     

Structural features of natural and acids modified chrysotile nanotubes

The structural features of the natural chrysotile have been studied by transmission electron microscopy, scanning electron microscopy, energy-dispersive X-ray spectrometry, thermogravimetric and low-temperature nitrogen adsorption techniques. The chrysotile fibers are present as nanotubes of cylindrical morphology of various forms (rectilinear cylinders, cylinders with cup-like ends, tube twins, cylinder-in-cylinder and cone-in-cone tubes) with the outer diameters of 15-30 nm and the inner ones of 2-6 nm. The surface areas of the raw and the acid leached chrysotile samples obtained by nitrogen adsorption are 15.3 and 63.6 m²/g with the average pore diameter 9.8 and 3.9 nm, respectively. The inner and the outer surfaces of the chrysotile nanotubes are evaluated by the geometric method as 16 and 80 m²/g. The thermogravimetric analysis reveals two main phases of mass loss associated with dehydration and dehydroxylation (with two overlaying steps) processes. The first phase is attributed to the dehydration reaction at low temperature range 293-450 K with activation energy in the range 22-32 kJ/mol. The second phase occurs between 798 and 985 K with activation energy 249-298 kJ/mol for the raw sample and 130-146 kJ/mole for the acid treated one.     

Multiple ionic-plasmon resonances in naturally occurring multiwall nanotubes: infrared spectra of chrysotile asbestos

Chrysotile asbestos is formed by densely packed bundles of multiwall hollow nanotubes. Each wall in the nanotubes is a cylindrically wrapped layer of Mg(3)Si(2)O(5)(OH)(4). We show by experiment and theory that the infrared spectra of chrysotile present multiple ionic-plasmon resonances in the Si-O stretching bands. These collective charge excitations are universal features of the nanotubes that are obtained by cylindrically wrapping an anisotropic material. The multiple plasmons can be observed if the width of the resonances is sufficiently small as in chrysotile.     

Improved surface morphology of flow-modulated MOVPE grown AIN on sapphire using thin medium-temperature AIN buffer layer

High-temperature (HT) AIN films were grown on (0 0 0 1) sapphire by low-pressure flow-modulated (FM) metal organic vapor phase epitaxy (MOVPE) with and without inserting a thin medium-temperature (MT) AIN layer. To suppress parasitic reactions between the sources of trimethylaluminum (TMA) and ammonia (NH₃), TMA and NH₃ was introduced to the reactor of MOVPE by alternating supply way. Surface morphology and crystalline quality were characterized by a scanning electronic microscopy (SEM), atomic force microscopy (AFM) and X-ray rocking curve (XRC) measurements of (0 0 0 2) and (10-12) diffractions. The AFM and SEM measurements indicated that the thin MT-AIN layer had a strong influence on the surface morphology of the HT-AIN films. The surface morphology became quite smooth by inserting the thin MT-AIN layer and surface RMS roughness values were 0.84 nm and 13.4 nm for the HT-AIN films with and without inserting the thin MT-AIN buffer layer, respectively. By etching the samples in aqueous KOH solution, it was found that the polarity of AIN films was different, the HT-AIN film with the thin MT-AIN layer could not be etched, indicating that the film had an Al-polar surface; however, the film without the MT-AIN layer was etched, which was explained that that film had a N- or mixed-polar surface. The mechanism for the origin of the different polarity of HT-AIN with and without the thin MT-AIN layer was proposed and discussed in detail.     

银纳米立方三维SERS基底制备及用于多种溶剂中农药的快速检测

使用种子生长法制备得到银纳米立方,扫描电镜的表征结果表明制备得到的银纳米立方尺寸为(61.5±4.4) nm,相对标准偏差为7.2%。利用表面替换技术将其表面的CTAC替换为更有利于SERS检测的柠檬酸根。然后基于具有超润滑特性的SLIPS衬底,构建出以银立方作为组装单元的具有三维热点的SERS基底。利用该三维SERS基底分别检测了水中的三环唑和乙醇中的福美双,检测限分别可达到52.8和41.6 nmol·L-1。实验结果表明银立方三维热点SERS基底具有较高的灵敏度,能够应用于多种溶剂中农药的快速检测,对于实际场景下农药残留的快速检测具有重要的意义。     

Etude de l'adsorption de monocouche a l'interface solide-solution diluee par spectroscopie de photoelectrons (XPS): Application a l'adsorption de phospholipides sur des fibres damiante

The adsorption of phospholipids on asbestos chrysotile in a solid-dilute-solution system has been studied by X-ray photoelectron spectroscopy (XPS). Two batches with different particle sizes were used: with thin and long fibres (SFA), and with short fibres (FCC). The fibres were analysed on a portion of filter after filtration. This method of sample preparation results in good reproducibility of the absolute intensities of the XPS peaks. Under these conditions, the surface coverage for monolayer adsorption was determined using an overlayer model. Comparison of the results deduced from the XPS data with those obtained from chemical analysis shows that for low initial concentrations of phospholipids, a different mode of adsorption occurs on the FCC fibres.     

Specific features of observing magnetization inhomogeneities on the surface of permalloy thin films by means of highly sensitive magnetic-force-microscopy probes

The results of studying regions of inhomogeneous magnetization on the surface of permalloy thin films with the use of fabricated highly sensitive probes of magnetic force microscopy (MFM) are presented. The technological features of manufacturing MFM probes with a high sensitivity to magnetic-field gradient are analyzed. Regions of ordering of the vertical component of the magnetic field are revealed, and domain walls are visualized in the thin films under study. Nanoscale measurements of the domain-wall thicknesses are performed.     

Generation of second optical harmonic in a macroscopic array of parallel nanowires

The quadratic optical susceptibility tensor for a macroscopically ordered array of parallel nanowires is determined. An experimental investigation of the polarization properties of signals of the second harmonic from ferroelectric nanowires synthesized in channels of chrysotile asbestos demonstrate that its results can be useful in structural studies.