Raman spectra of Graphon carbon black

The Raman spectrum of Graphon carbon black has been recorded using rotating cell techniques. Angular dependence of scattering at 1360, 1580 and 2700 cm^?1 are reported and these data suggest that the 1360 cm^?1 line is associated with non-planar microstructure distortions. The excitation frequency dependence of the intensity ratio of the bands at 1360 (D) and 1580 cm^?1 (G) is interpreted in terms of resonance (vibronic) interaction. This dependence is primarily the result of an increase in the intensity of the 1360 cm ^?1 line. The disorder-associated line (D) exhibits a significant excitation-dependent shift from 1378 cm^i?1 (457.9 nm Ar⁺) to 1330 cm^?1 (647.1 nm Kr⁺). The “graphite” (G) line position is less sensitive to changes in excitation frequency. The spectral features are discussed in terms of factor group, C_6v⁴, and layer site symmetry, C_3v. Also the possible role of localized alkene-like structure in zones of structural distortion is considered.     

Transferring information from one experiment to another

This paper presents a rational method (based on Bayes' Theorem) for transferring information on parameter values from one experiment to another, in situations where the mathematical models for the two experiments share some parameters in common. The uncertainty in the estimates of the parameters, which reflects the experimental error in the initial experiment, is properly transferred as well. The use of the method is demonstrated by applying it to a fairly complicated system, typical in chemical reaction engineering, in which the kinetic parameters in a model for the hydrogenolysis of butane reaction were estimated using data obtained from a bench-scale, integral packed-bed reactor. These parameter estimates were then transferred to a model for a fluidized bed reactor in which the same chemical reaction occurred. Using the fluidized bed data they were updated and two additional parameters in the fluidized bed model were also estimated. This procedure allows a more realistic estimate of the uncertainty in all parameter values in the model for the fluidized bed reactor.     

In situ polymerization and nano‐templating phenomenon in nylon fiber/PMMA composite laminates

Supercritical Carbon Dioxide (SC CO₂) is used as a reaction/processing medium in the fabrication of fiber‐reinforced composite materials. SC CO₂ allows resin (reactive monomer), to penetrate inside the fibers themselves, partitioning into the amorphous regions of the fiber. The crystal structure then templates polymerization of matrix within the fiber. This process produces a composite that exhibits ultralong‐range order from the nanoscale reinforcement of crystals to the macroscale fiber reinforcement of matrix. In addition, SC CO₂ lowers resin viscosity and aids in wetting out Nylon 6,6 fiber reinforcement in a process similar to reaction injection molding (RIM) or resin transfer molding (RTM). This article will discuss the fabrication technique in detail, including process parameters and the structure of resulting composites and morphology of modified fibers. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 1600–1607, 2003     

Molecular sieve properties obtained by cracking of methane on activated carbon fibers

Molecular sieve properties of activated carbon fibers modified by cracking treatment with methane are studied herein. The effect of methane treatment on the porous texture of the samples has been studied while varying temperature and time. These materials have been evaluated for their selectivity during CO₂ and CH₄ separation; their uptakes have been compared with non-treated activated carbon fibers (studied previously), which were considered suitable to be used as molecular sieves. Kinetics of CO₂ and CH₄ uptake have also been investigated in this research. The treatment produced materials exhibiting fast kinetics and high selectivity during CO₂ and CH₄ separation; at the same time however, the CO₂ uptake capacity was diminished.     

Synthesis of polycarbonate containing in-chain 4-N,N-dimethylamino-4′-nitrostilbene via ring-opening polymerization

Summary We have successfully synthesized a new NLO chromophore based on 4-N,N-dimethylamino-4-nitrostilbene which contains bisphenol functionality for polycarbonate preparation. Chromophore-4 was used to make macrocyclic carbonate oligomers and the oligomers were converted to polycarbonate via ring-opening polymerization in solution.     

ELECTROKINETIC EFFECTS: CARBONIC ANHYDRASE AND CO2 ELECTRODE DYNAMICS

It is well known that the dynamic response rate of the Severinghaus-type CO₂ electrode is improved significantly in some cases by addition of the enzyme carbonic anhydrase to the electrode assembly. Hysteresis in the response rate also is reduced. Experimental data and modelling results indicate that catalysis of the CO₂ hydration reaction in the bulk of the bicarbonate layer (the Nernst film) is not responsible for the improved response behavior, Evidence is presented to show that catalysis in the electrostatic double layer region at the glass electrode surface is a possible explanation. This proposed phenomenon may have widespread implications for the optimal design of analytical devices, commercial processes involving electrochemical phenomena, and may also provide insight into electrobiologi-cal processes.     

Transparent,methacrylate-based polymer networks with controlled crosslinker ductility

A series of transparent methacrylate-based crosslinked polymer networks are prepared in which the crosslinker length is controlled as a means to investigate the effects of network ductility on mechanical and ballistic properties. In each network the optical clarity of pure poly(methyl methacrylate) (PMMA) is retained, as well as a low value of haze. Both the glass transition temperature (T_g) and the tensile modulus of the networks are highly tunable, with network values both above and well below that of pure PMMA or the pure crosslinker network. The ballistic performance is likewise affected, with performance values of up to 400% greater than neat PMMA. We examine the effects of the crosslinker molecular weight on the impact performance, finding that, in these systems, the molecular weight between crosslinks is not a driving factor for the impact performance, and this may broadly translate to polymer networks in general. We find that improvements in ballistic performance can be realized at low molecular weight between crosslinks, provided the crosslinking agent is of sufficient ductility.     

Microstructure, mechanical and tribological properties of Cr1−xAlxN films deposited by pulsed-closed field unbalanced magnetron sputtering (P-CFUBMS)

Nanocrystallized Cr_1−xAl_xN films with various Al contents (0 to 68 at.%) were deposited by pulsed closed field unbalanced magnetron sputtering (P-CFUBMS). The effects of aluminum content on the microstructure, mechanical and tribological properties of the Cr_1−xAl_xN films have been investigated. It was found that the hardness and elastic modulus of Cr_1−xAl_xN films increased with increasing Al contents in the films and reached the highest value of 36 GPa and 370 GPa, respectively, at an Al content of 58.5 at.%. Addition of Al beyond 64.0 at.% resulted in a change in crystal structure from B1 cubic to B4 hexagonal phase. The wear resistance improved gradually with the increase of Al in the Cr_1−xAl_xN films. A combination of the abrasive and adhesive wear mechanism was proposed based on the SEM and EDS analysis of the wear track. The steady state dry coefficient of friction measured against a WC ball for the Cr_1−xAl_xN films were in the range of 0.36-0.55, and the wear rate was in the 10^− 6 mm³ N^− 1 m^− 1 range.     

Elemental Powder Approaches to Ni3Al-Matrix Composites

Reactive sintering and hot isostatic compaction of mixed elemental powders have been combined to fabricate full density NiAl intermetallic-matrix composites. This process involves the formation of the matrix compound from its elemental constituents through an exothermic reaction. Dispersed ceramic phases inhibit direct consolidation, necessitating superposition of external pressure via hot isostatic compaction to obtain full density. The latter process is termed reactive hot isostatic pressing (RHIP). Because of its flexibility and low cost, this fabrication process merits attention as a means of preparing monolithic compounds and intermetallic-matrix composites.