Tensile properties of long aligned double-walled carbon nanotube strands

The mechanical properties of well-aligned double-walled carbon nanotube (DWNT) strands with diameters of 3-20 μm and lengths of ∼10 mm were measured using a stress-strain puller. The average tensile strength and Young’s modulus of the tested strands are 1.2 GPa and 16 GPa, respectively. Deformation and fracture processes of these samples are discussed. The tensile strength and Young’s modulus of an individual DWNT bundle were estimated, with values comparable to those of SWNT bundles. The superior mechanical strengths of our as-prepared DWNT strands are expected to give them potential as a high-strength material and a reinforcement in composites.     

Mass production of high-quality multi-walled carbon nanotube bundles on a Ni/Mo/MgO catalyst

A new catalyst (Ni/Mo/MgO) is reported, with which one can synthesize multi-walled carbon nanotube (MWNT) bundles with a yield of more than 45 times the amount of the pristine catalyst, using a methane-hydrogen mixture as precursor. Powder X-ray diffraction, Raman spectroscopy and thermal gravimetric analysis show that the purity of the as-prepared MWNTs is over 97%. The diameter of the carbon nanotubes is 9-20 nm, measured by high-resolution electron microscopy on 421 individual MWNTs. The high purity of the as-prepared MWNTs allows us to omit the usual complex purification process required for carbon nanotubes synthesized by chemical vapor deposition. Because of its durable high activity, the Ni/Mo/MgO catalyst in its pristine state is ideal for mass production of high-quality MWNTs. The synergism of nickel and molybdenum is considered the main reason for the high yield of carbon nanotubes.     

Improved activated carbon by thermal treatment in methane and steam: Physicochemical influences on MIB sorption capacity

Thermal treatment by steam or by methane plus steam altered the physicochemical properties of a commercial lignite-based activated carbon; and improved the carbon’s sorption capacity for the odorant 2-methylisoborneol (MIB). Rapid small scale column tests (RSSCTs) revealed that favorable thermal treatment allowed an activated carbon to remove this odorant for up to six times longer before initial MIB breakthrough than did its commercial lignite counterpart. For these RSSCTs (135 ppt), clarified water from a water treatment plant (2.07 mg/L TOC) was spiked with ¹⁴C-MIB; and liquid scintillation protocols facilitated ¹⁴C-MIB detection at 1-3 ppt. The more favorable thermal treatment at 1000 °C increased pore volumes with 5-400 Å widths by twofold; and the bed volume to initial MIB breakthrough correlated fairly well (R² = 0.9) with pore volume in the range of 5-60 or 5-400 Å. Thermal tailoring altered the carbon’s apparent point of zero charge: from pH 6.5 for the commercial lignite carbon, to pH 9.2 for tailored carbon. When methane and steam were used together, the C, H, N and O contents were virtually the same as for the commercial lignite. In contrast, when steam was employed alone, the percent of oxygen increased, and the percent of H, C and N therefore decreased slightly.     

Diameter control of carbon nanotubes by changing the concentration of catalytic metal ion solutions

We have developed a simple new method to control the diameter of carbon nanotubes (CNTs) using catalytic nanoparticle arrays fabricated by filling the pores of well-ordered porous anodic aluminum oxide (AAO) templates with a metal ion solution. Fe ion solution was used to fill the pores in which Co had been deposited electrochemically, and then the template was dried naturally on a magnet. After this process, the pores were widened in NaOH solution. Well-graphitized multi-walled CNTs were grown from almost all the pores and were very long in length and homogeneous in diameter. We were able to control the diameter of CNTs, simply, by changing the concentration of iron ion solution. For example, the average outer diameters of the CNTs are 7 ± 1.5, 13 ± 1, and 17 ± 1 nm when the concentrations of Fe ion in their mother solutions were 1.0 × 10⁻³, 3.0 × 10⁻³, and 6.0 × 10⁻³ M, respectively. The inner diameters of these CNTs corresponded to the calculated diameters of Fe nanoparticles by assuming that all Fe ions contained in each pore are reduced to a single nanoparticle. This means that homogeneous nanoparticles are made in each pore. Our new method could be used to fabricate homogeneous nanoparticles from most metal ion solutions.     

Polarization dependent optical absorption properties of single-walled carbon nanotubes and methodology for the evaluation of their morphology

Polarization dependence of the optical absorption properties of SWNTs is presented and investigated in detail for the energy range 0.5-6 eV. We found that the absorption peaks in the UV region at approximately 4.5 and 5.25 eV exhibit remarkable and different dependencies on the morphology of the SWNT film, or equivalently, on the incident light polarization relative to the SWNT axis. An analytical pathway to evaluate the physical degree of SWNT alignment for a vertically aligned SWNT film is developed with both transition dipoles parallel and perpendicular to the SWNT axis taken into account. This analytical procedure, coupled with polarized optical absorption measurements performed on the vertically aligned SWNT film grown on substrates, leads to the determination of the bare optical absorption cross-section of SWNTs for both parallel and perpendicular to SWNT axis. In the end, the proposed methodology for evaluating the SWNT film morphology is applied to investigate the transient change of the degree of alignment in the growth process of our vertically aligned SWNT films.     

Effects of buffer layer materials and process conditions on growth mechanisms of forming networks of SWNTs by microwave plasma chemical vapor deposition

This study investigates the growth mechanism of IC compatible processes and to the feasibility of synthesizing networks of single-walled carbon nanotubes (SWNTs) at lower temperatures (610 °C) on Si wafer using microwave plasma chemical vapor deposition (MPCVD) with CH₄ and H₂ as source gases. The effects of the buffer layer materials (ZnS–SiO₂, Al₂O₃, AlON, and AlN ) and process conditions on growth of carbon nanostructures with Co as catalyst were also examined, where the buffer layers and Co catalyst were deposited in sequence by physical vapor deposition (PVD), followed by H-plasma pretreatment before deposition of carbon nanostructures. Additionally, the morphologies and bonding structures of carbon nanostructures were characterized by field emission scanning electron microscopy (FESEM), high resolution transmission electron microscopy (HRTEM), and Raman Spectroscopy. Analytical results demonstrate that networks of SWNTs are more favorable to be synthesized by selecting proper buffer layer material (e.g., AlON), and under higher temperatures, thinner catalyst thickness (e.g., 5 nm) and lower CH₄ / H₂ ratio (e.g., 5 / 100 sccm/sccm). The networks of SWNTs can be fabricated at temperatures as low as 610 °C by manipulating these parameters. In conclusion, the growth mechanism determines the conditions for the formation of nano-sized extrusions on catalyst particles surface.     

Effect of TiO2 thin film thickness and specific surface area by low-pressure metal–organic chemical vapor deposition on photocatalytic activities

TiO₂ photocatalyst films having an anatase crystal structure with different thickness were prepared by the low-pressure metal–organic chemical vapor deposition (LPMOCVD) to examine the effect of growth conditions on photocatalytic activity. Film thickness was linearly proportional to the deposition time. Structure of the film was strongly dependent on the deposition time. In early stage of deposition, fine particles deposit on the substrate. As increasing the deposition time, crystal orientation is gradually selected following the Kolmogorov model and c-axis oriented columnar crystals become dominant. The photocatalytic activity strongly depends on the film deposition time (or film thickness) in nonlinear way. The optimum thickness of TiO₂ catalyst film grown by LPMOCVD may locate between 3 and 5 μm.     

Performance of fluorine-added CoMoS/Al2O3 prepared by sonochemical and chemical vapor deposition methods in the hydrodesulfurization of dibenzothiophene and 4,6-dimethyldibenzothiophene

The performance of a new type of CoMoS/Al₂O₃ catalyst, with added fluorine and prepared by sonochemical and chemical vapor deposition (CVD) methods, was investigated in the hydrodesulfurization (HDS) of dibenzothiophene (DBT) and 4,6-dimethyldibenzothiophene (4,6-DMDBT). The catalyst, which was designed to contain optimum amounts of fluorine and cobalt, exhibited a higher activity, ca. 4.6 times higher activity particularly in the HDS of 4,6-DMDBT, than a fluorine-free catalyst prepared by a conventional impregnation method. The enhanced activity of the new catalyst can be attributed to the cumulative effects of individual factors involved in the catalyst preparation. That is, the use of a sonochemical synthesis led to a high dispersion of small MoS₂ crystallites on the alumina, and the addition of the Co species to the catalyst by CVD caused a close interaction between the Co species and the MoS₂ crystallites to produce numerous CoMoS species, which are the catalytically active species for HDS. The addition of fluorine increased the amounts of acidic sites in the catalyst, which promoted hydrogenation (HYD) route to a greater extent than the direct desulfurization (DDS) route in DBT HDS and both HYD and DDS routes to similar extents in the case of 4,6-DMDBT HDS. Accordingly, the addition of fluorine led to a greater increase in catalytic activity for 4,6-DMDBT HDS than for DBT HDS.     

从强制循环到高电流密度自然循环电槽的改造

介绍国内第一套国产高电流密度自然循环离子膜电解槽装置的设计及运行情况。通过改造,装置的生产能力大幅度提高。     

老化试验中PE-HD的结构与力学性能研究

研究了高密度聚乙烯在海南自然曝露和氙灯人工老化后的结构和力学性能变化。结果表明：相比于自然曝露，高密度聚乙烯主要力学性能的氙灯人工老化加速倍率大约为4；老化期间，高密度聚乙烯分子间存在着交联和降解二种竞争反应，老化早期以交联为主，后期以降解为主；氙灯老化试验相比于自然曝露，老化主要集中在材料表层。