Graphitization of polyacrylonitrile carbon fibers and graphite irradiated by γ rays

To investigate the effect of γ-ray radiation on the microstructure of carbon fibers (CF) and graphite, the carbon fibers and graphite were irradiated by ⁶⁰Co source at room temperature. X-ray diffraction results indicate that the interlayer spacing d₀₀₂ of CF and graphite decreased after irradiation. The intensity of (002) peak in CF decreased while the peak of the (002) plane in graphite becomes sharper after irradiation. Scanning electron microscopy combined with energy dispersive X-ray spectroscopy determines that γ-ray irradiation slightly improves the carbon content of CF surface layer. Compton scattering effect and heating caused by γ-ray are proposed to be responsible for the graphitization of CF and graphite.     

Solid-state 13C NMR of carbon nanostructures (milled graphite,graphene, carbon nanotubes,nanodiamonds, fullerenes) in 2000–2019: a mini-review

Abstract

A brief overview is given of the papers published over the last two decades on the subject of solid-state ¹³C NMR spectra of such carbon nanostructures as milled graphite and its oxide, graphene, graphene oxide, carbon nanotubes, nanodiamonds, fullerenes and their derivatives. The main focus is put on the characteristic values of experimental isotropic ¹³C NMR chemical shifts and their interpretation in terms of local chemical environments of carbon nuclei.     

Hydrothermal synthesis of β-nickel hydroxide nanocrystalline thin film and growth of oriented carbon nanofibers

Novel well-crystallized β-nickel hydroxide nanocrystalline thin films were successfully synthesized at low temperature on the quartz substrates by hydrothermal method, and the oriented carbon nanofibers (CNFs) were prepared by acetylene cracking at 750 °C on thin film as the catalyst precursor. High resolution transmission electron microscopy (HR-TEM) measurement shows that thin films were constructed mainly with hexagonal β-nickel hydroxide nanosheets. The average diameter of the nanosheets was about 80 nm and thickness about 15 nm. Hydrothermal temperature played an important role in the film growth process, influencing the morphologies and catalytic activity of the Ni catalysts. Ni thin films with high catalytic activity were obtained by reduction of these Ni(OH)₂ nanocrystalline thin films synthesized at 170 °C for 2 h in hydrothermal condition. The highest carbon yield was 1182%, and was significantly higher than the value of the catalyst precursor which was previously reported as the carbon yield (398%) for Ni catalysts. The morphology and growth mechanism of oriented CNFs were also studied finally.     

Influence of material and process parameters on microstructure evolution during the fabrication of carbon–carbon composites: a review

Journal of Materials Science - Carbon–carbon composites (CCCs) are a unique form of carbon fiber-reinforced materials that exhibit excellent thermomechanical properties under extreme...     

Evaluation across and within collaborative manufacturing networks: a comparison of manufacturers’ interactions and attributes

Evaluation on collaborative manufacturing network (CMN) structure characteristics has important implications for network operations such as production decision-making, product recovery, creating consensus. Several recent studies suggest that augmenting network structure with nodes’ attributes can provide a more fine-grained understanding of the network. However, there have been few studies to provide a systematic understanding of these effects in a CMN at scale. This gap is bridged using an industrial printing machinery CMN data-set collected on a web-based producing and outsourcing service platform. Novel phenomena with respect to both interaction and attribute metrics across and within the CMNs are observed. Moreover, although many studies employ either interaction or attribute data to study the relative roles of manufacturers in a CMN, relatively little is known about the relationship between these two types of data. This study explores this relationship by comparing two defined metrics (i.e. relational capability and node capability), which evaluate the manufacturers’ interactions and attributes, respectively. We examine to what extent the two metrics of manufacturers correlate with each other, and how possible dissimilarities and similarities can be explained based on the collected industrial CMN data-set. The insights thereby provide a better basis for efficient operations decision-making in CMN.     

Calculated NMR chemical shifts of nylon 6: a comparison of the α and γ forms

The ¹³C and ¹⁵N chemical shifts of the and crystal forms of nylon 6 have been estimated using ab initio calculations (GIAO method) with the B3LYP Density Functional and the 6-311G(d) basis set. Calculations were applied on proper model systems and the agreement with experimental data was quite good in all cases. Comparison between the results obtained for isolated chains and hydrogen bonded sheets allowed to elucidate the influence of the conformation and packing forces in the chemical shifts. These results open up new opportunities for the future use of quantum mechanical calculations as a complementary tool in the determination of the crystal structure of polymers.     

Electrocatalytical oxidation and sensitive determination of acetaminophen on glassy carbon electrode modified with graphene–chitosan composite

The electrochemical behaviors of acetaminophen (ACOP) on a graphene–chitosan (GR–CS) nanocomposite modified glassy carbon electrode (GCE) were investigated by cyclic voltammetry (CV), chronocoulometry (CC) and differential pulse voltammetry (DPV). Electrochemical characterization showed that the GR–CS nanocomposite had excellent electrocatalytic activity and surface area effect. As compared with bare GCE, the redox signal of ACOP on GR–CS/GCE was greatly enhanced. The values of electron transfer rate constant (k_s), diffusion coefficient (D) and the surface adsorption amount (Γ^?) of ACOP on GR–CS/GCE were determined to be 0.25 s^? 1, 3.61 × 10^? 5 cm² s^? 1 and 1.09 × 10^? 9 mol cm^? 2, respectively. Additionally, a 2e^?/2H⁺ electrochemical reaction mechanism of ACOP was deduced based on the acidity experiment. Under the optimized conditions, the ACOP could be quantified in the range from 1.0 × 10^? 6 to 1.0 × 10^? 4 M with a low detection limit of 3.0 × 10^? 7 M based on 3S/N. The interference and recovery experiments further showed that the proposed method is acceptable for the determination of ACOP in real pharmaceutical preparations.     

Nanoscale characterization of gold colloid monolayers: a comparison of four techniques

Atomic force microscopy (AFM), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), and near-field scanning optical microscopy (NSOM) have been used to characterize the nanostructure of Au colloid-based surfaces. Because these substrates are composed of particles whose dimensions are known prior to assembly, they are well-suited for a critical comparison of the capabilities and limitations of each nanoscale imaging technique. The three criteria for this comparison, which are relevant to the field of nanoparticle assemblies in general, are (i) accuracy in establishing particle size, particle coverage, and interparticle spacing; (ii) accuracy in delineating surface topography; and (iii) ease of sample preparation, data acquisition, and image analysis. For colloidal Au arrays, TEM gives the most reliable size and spacing information but exhibits the greatest constraints with regard to sample preparation; in contrast, AFM is widely applicable but yields data that are the least straightforward to interpret. For accurate information regarding nanometer-scale architecture of particle-based surfaces, a combination of at least one scanning probe method (AFM, NSOM) and one accelerated-electron method (TEM, FE-SEM) is required.     

Synthesis,characterization and comparison of polythiophene–carbon nanocomposite materials as Pt electrocatalyst supports for fuel cell applications

A novel polymer–carbon (PTh–C) nanocomposites containing different percentages of polythiophene (10, 20 and 50% (w/w)) and carbon (Vulcan XC-72) was prepared by a facile solution dispersion method and used to support platinum nanoparticles. The effect of using different percentages of polythiophene in nanocomposites and subsequently prepared electrocatalysts was investigated. The resultant electrocatalysts were extensively characterized by physical (X-ray diffraction (XRD) and transmission electron microscopy (TEM)) and electrochemical (cyclic voltammetry (CV)) techniques. The TEM results showed that the fine Pt nanoparticles prepared by ethylene glycol (EG) method were distributed on the surface of the 50% PTh–C nanocomposites successfully. From the XRD patterns, the average size of dispersed Pt nanoparticles with the face-centered cubic (fcc) structure on 50% PTh–C, 20% PTh–C, 10% PTh–C and carbon were about 4.9, 5.2, 5.4 and 6.1 nm, respectively. The conductivity of PTh–C with different percentages of pure PTh was compared with the conductivity of the corresponding support of pure PTh. It is observed that the conductivity of 50% PTh–C nanocomposites is about 600 times higher than that of pure PTh. Finally, CV measurements of hydrogen and methanol oxidations indicated that Pt/50% PTh–C had a higher electrochemical surface area and higher catalytic activity for methanol oxidation reaction compared to other electrocatalysts. These measurements showed that the Pt/50% PTh–C electrocatalyst by the value of 3.85 had higher \(I_{\mathrm{f}}/I_{\mathrm{b}}\) ratio with respect to Pt/10% PTh–C and Pt/20% PTh–C by the values of 2.66 and 2.0, respectively.     

Effects of boron,carbon, and silicon additions on microstructure and properties of a Ti–15Mo based beta titanium alloy

Abstract

Additions of boron, carbon, and silicon have been made to a series of Ti–15Mo based β titanium alloys prepared by plasma arc melting and subjected to various processing and characterisation techniques. The purpose of these additions was to investigate their grain refining effect in the as cast, as forged, and heat treated states. The boron and carbon additions promoted dendritic solidification. Boride and carbide particles were present in the interdendritic regions. However, a fully equiaxed fine grained structure could not be obtained even at the highest levels of addition (1.0 wt-%). These additions resulted in substantial microstructural refinement after forging and the particles stimulated the nucleation of recrystallised grains. Significant retardation of grain growth was observed after solution treatment and attributed to the Zener pinning effects of the boride and carbide particles. Despite the microstructural refinement, the ductility of the alloys containing boron and carbon was severely impaired.     

Electrostatic spraying: a novel technique for preparation of polymer coatings on electrodes

A liquid flow emerging from a tip or a thin tube under the influence of a strong electric field will, due to charging of the dielectric liquid, break up into small droplets. Thus, if a polymer material is dissolved in the liquid, this electrodeposition technique can be utilized for producing polymer coatings on electrodes. The method was applied for in situ formation of ultrathin (～3000 ?) cellulose acetate (CA) phase inversion membranes on glassy carbon electrodes. The purpose of the membrane was to protect the electrode surface from fouling by macromolecular species. The spraying liquid consisted of CA, acetone, and aqueous magnesium perchlorate as pore former, and the spraying voltage was 14 kV. Profilometric measurements showed that the thickness of the spray-cast membranes was much more uniform than that of similar membranes formed by solvent casting. By using cadmium and lead as test analytes and differential pulse anodic stripping voltammetry as detection method, it was found that the membranes prepared by spray casting offered better protection against interference from poly(ethylene glycol) (PEG) 6000 than those prepared by solvent casting. Also, the interference from PEG 2000 was significantly reduced. Experimental details of the electrostatic spraying technique are given.     

Diffusion of carbon and titanium in γ -iron in a magnetic field and a magnetic field gradient

The diffusion coefficients of carbon and titanium in γ -iron were measured in a 6T magnetic field and in magnetic field gradients ranging from 30 to 45 T/m. We have found that the diffusion of carbon in γ -iron is retarded by application of a 6T magnetic field. In contrast with carbon diffusion, no noticeable effect of a magnetic field on the diffusivity of titanium in γ -iron is observed. On the other hand, the diffusion of carbon in γ -iron can be enhanced in a magnetic field gradient when carbon atoms move towards the direction with a higher magnetic field strength. The higher the magnetic field gradient strength becomes, the more the carbon diffusion is enhanced. Nevertheless, a magnetic field gradient causes a decrease in diffusivity of carbon in γ -iron when the opposite magnetic field gradient is applied.     

Two features of the uniaxial compression of a glassy epoxy resin: the yield stress rate-dependence and the volumetric instability

We report the results of uniaxial compressive tests on a DGEBA epoxy resin at room temperature, well below its glass transition. We first focus on the strength, defined as the stress value corresponding to either a maximum or a flattening of the stress-strain curve, which, for this polymer, may be taken to be coincident with the yield stress, as often assumed for many thermosets. Within the strain rate range (1.E?6 s^?1, 2.E?3 s^?1) we confirm the linear trend relating the logarithm of the strain rate to the yield stress, as already been observed by other investigators even for the same epoxy resin; instead, at strain rates below \(\dot{\varepsilon} _{0} \approx 1.\mathrm{E}{-}6~\mathrm{s}^{-1}\), we found a negligible rate-dependence, as our data indicate a lowest limit of the yield stress, of about 87 MPa. On the basis of these results, we propose how to extend to the viscoplastic regime of deformation a nonlinear viscoelastic model previously put forward.Secondarily, within the viscoelastic range, at a stress level significantly lower than the yield stress, our measurements show a mild volumetric instability, allowed by the free lateral expansion, not ascribable to any macroscopic structural effect; such a behaviour has never been reported in the literature, to the best of our knowledge.     

Highly sensitive amperometric sensor for micromolar detection of trichloroacetic acid based on multiwalled carbon nanotubes and Fe(II)–phtalocyanine modified glassy carbon electrode

A highly sensitive electrochemical sensor for the detection of trichloroacetic acid (TCA) is developed by subsequent immobilization of phthalocyanine (Pc) and Fe(II) onto multiwalled carbon nanotubes (MWCNTs) modified glassy carbon (GC) electrode. The GC/MWCNTs/Pc/Fe(II) electrode showed a pair of well-defined and nearly reversible redox couple correspondent to (Fe(III)Pc/Fe(II)Pc) with surface-confined characteristics. The surface coverage (Γ) and heterogeneous electron transfer rate constant (k_s) of immobilized Fe(II)–Pc were calculated as 1.26 × 10^? 10 mol cm^? 2 and 28.13 s^? 1, respectively. Excellent electrocatalytic activity of the proposed GC/MWCNTs/Pc/Fe(II) system toward TCA reduction has been indicated and the three consequent irreversible peaks for electroreduction of CCl₃COOH to CH₃COOH have been clearly seen. The observed chronoamperometric currents are linearly increased with the concentration of TCA at concentration range up to 20 mM. Detection limit and sensitivity of the modified electrode were 2.0 μM and 0.10 μA μM^? 1 cm^? 2, respectively. The applicability of the sensor for TCA detection in real samples was tested. The obtained results suggest that the proposed system can serve as a promising electrochemical platform for TCA detection.     

Fabrication and oxidation behavior of a reaction derived graphite–ZrC composite for ultrahigh temperature applications

Graphite containing nominally 40 vol.% ZrC (graphite–ZrC) was prepared from commercially available ZrO₂ and graphite powders by hot pressing at 2000 °C in a vacuum. The oxidation behavior of the graphite–ZrC composite was carried out in dry stagnant air at the temperatures of 1200 and 2200 °C. Compared with the pure graphite, the graphite–ZrC composite exhibited good oxidation resistance because the mass loss of the composite powder was significantly lower than that of the pure graphite. The mass loss of graphite–ZrC at 2200 °C was lower than pure graphite at 1200 °C. Furthermore, the introduction of ZrC also improved the strength of the graphite–ZrC composite.