The synergistic performance of multiwalled carbon nanotubes and sepiolite nanoclays as flame retardants for unsaturated polyester

The synergistic effect on the thermal decomposition and heat release rate (HRR) in particular the peak heat release rate (PHRR) of unsaturated polyester (UP) resin blended with multiwalled carbon nanotubes (MWNTs) and sepiolite nanoclay was investigated using thermal gravimetric analysis (TGA), pyrolysis combustion flow calorimetery (PCFC) and the cone calorimetery. Initial microcalorimeter findings established a synergistic effect for ternary system comprising a 10:0.5 wt% mixture of sepiolite:MWNT, respectively, which resulted in a 40% reduction in heat release capacity (HRC). This result was also confirmed within the well‐established cone calorimeter by a 50% reduction in PHRR in contrast to unfilled UP. The mechanism behind this reduction is thought to be due to the bridging of the MWNTs between the sepiolite clay needles, creating a tight protective surface layer that reduces the MLR. TGA also confirmed the advantage of such a ternary system through a 36^°C shift in the onset decomposition temperature and an 11% increase in residual char. Copyright © 2010 John Wiley & Sons, Ltd.     

Structural and functional analogy between pneumolysin and proaerolysin

Pneumolysin and proaerolysin are bacterial toxins that form pores in host cells by oligomerization. We propose that they may have similar structures despite a poor sequence identity. The crystal structure of proaerolysin reveals a protein composed of four domains, arranged in the shape of an elongated comma. Electron microscopy of the pneumolysin monomer shows a similar arrangement of domains. The sequence of pneumolysin recognizes the template of proaerolysin from a library of protein folds. A three-dimensional model of pneumolysin has been constructed by the comparative approach using the structure of proaerolysin. This model, together with results on the activity of site- specific mutants and the positions of antigenic sites, has been used to propose functional roles of individual domains.      

Non-uniformity of binder distribution in high-shear granulation

Further experimental investigation based on a microscopic, or single granule, scale has been conducted to investigate the uniformity of binder composition within a given size class for high shear melt granulation. This work assesses whether there is significant non-uniformity of binder composition within size classes to warrant considering this level of detail to improving population balance modelling of high shear granulation. It is concluded that at early times in a batch granulation process there is a broad variation in binder content between individual granules and that this variation persists in granules of small size.     

Fatigue Crack Growth of Peened Friction Stir-Welded 7075 Aluminum Alloy under Different Load Ratios

The effect of peening on the fatigue crack growth performance of friction stir-welded 7075 aluminum alloy was investigated. The fatigue crack growth rates were assessed for laser- and shot-peening conditions at stress ratios (R) of 0.1 and 0.7. The surface and through thickness residual stress distributions were characterized for the different regions in the weld. The results indicate a significant reduction in fatigue crack growth rates using laser peening compared to shot peening and the as-welded condition. The effect of the compressive stresses obtained through laser peening was deemed responsible for increasing the resistance to fatigue crack growth of the welds.     

Aqueous Ozonation Of Fatty Acids

The reactivity of a series of fatty acids toward ozone was examined in aqueous solution at low substrate concentration (μg.L^?1 range). Saturated fatty acids were unreactive, unsaturated fatty acids were readily consumed. A number of reaction products or their methylated derivatives were identified by gas chromatography and gas chromatography-mass spectrometry. The products identified are consistent with a 1,3-dipolar cyclo-addotion reaction.     

A new technique to derive particle size distributions and aerosol number concentrations directly from thermophoretic data

The manufacture of many high value-added powders takes place by the decomposition of gaseous precursors in aerosol tube reactors. Historically, process improvements were achieved by making changes on the outside of the reactor and observing what comes out at the end of the pipe. The development of increasingly accurate aerosol dynamics models based on engineering first principles has been limited because models were typically validated on integral properties of ex situ product, instead of particle properties measured at multiple positions inside the reactor. In this study, a model reactor was equipped to capture samples thermophoretically from 15 internal positions. Additional in-line measurements were achieved with a multi-stage inertial impactor and by traditional analysis of ex situ product. Calculations were performed to verify that thermophoresis was the dominant mechanism of particle capture. The thermophoretic samples were analyzed by electron beam microscopy and image analysis to develop particle size distributions at each of the internal positions inside the reactor. An approximation of Talbot's Equation for thermophoretic velocity allowed experimental measurements to be combined with thermophoretic sample data to give predictions of particle number concentration corresponding to the precise sampling locations. The combinations of particle size distributions and number concentrations provide powerful insights on particle nucleation and growth dynamics.     

Diamond-like carbon coating of alternative metal alloys for medical and surgical applications

The effectiveness of a plasma-deposited, diamond-like carbon (DLC) coating on aluminium alloy based surgical instruments is investigated. Surgical instruments must satisfy a number of important criteria including biocompatibility, functional performance, sterility and cleanability, structural integrity, and fatigue resistance. The integrity of the DLC layer and the diffusion barrier properties are of paramount importance due to biocompatibility considerations of the underlying aluminium metal. We investigate the optimisation of the coating with incorporation of silicon and variation in negative self bias, and highlight the design and manufacture of a lightweight laparoscopic assist instrument from aluminium alloy coated with diamond-like carbon, which has been used successfully in the clinical environment to improve operations such as cholecystectomy (gall bladder removal) and exploratory techniques for the diagnosis of cancer.     

EFFECTS OF ASPHALTENE PRECIPITATION AND REPRECIPTION ON THE METAL-CONTAINING COMPOUNDS IN HEAVY RESIDUA

ABSTRACT

Boscan vacuum residuum (VR) has been separated into isooctane insoluble asphaltenes and isooctane soluble maltenes. The asphaltenes were dissolved in a minimum of toluene and were further separated by two additional reprecipitations using isooctane as the precipitating solvent. We examined the fractions, including the recovered isooctane soluble material, by size exclusion chromatography (SEC) with inductively coupled plasma (ICP) emission spectroscopy to determine the effects, if any, the reprecipitations have on the size distribution of the metal-containing compounds.

The asphaltene fractions show little change in size upon reprecipitation, but removal of a small amount of the metal components does occur. The first reprecipitation produces isooctane soluble material which is very similar in size to the original maltene fraction. However, the second reprecipitation removes small amounts of material in the size range of the asphaltenes. When the amounts were weight balanced, the resulting separation did little to effect the overall maltene and asphaltene size profiles.     

CHARACTERIZATION OF NICKEL AND VANADIUM COMPOUNDS IN TAR SAND BITUMEN BY UV-VIS SPECTROSCOPY AND SIZE EXCLUSION CHROMATOGRAPHY COUPLED WITH ELEMENT SPECIFIC DETECTION

ABSTRACT

Previously, we have examined the Ni and V in heavy crude oils, residua, and processed products by several metal speciation techniques to ascertain molecular structure and processing behavior. Two classes of metal compounds were found -metallopetroporphyrins and metallo-nonporphyrins - each having unique reactivity during processing. In efforts to better understand the binding of metals in the oil medium, we have now examined Ni and V in tar sand bitumens, the bitumen was solvent extracted from the sand matrix and was separated by column chromatography and the petro-porphyrin content was quantitated by UV-vis spectroscopy. The petroporphyrin contents ranged from virtually none to over 36% of the total metals. Asphalt Ridge (Utah) has primarily Ni petroporphyrins; Big Clifty (Kentucky) and Athabasca (Canada) have primarily V petroporphyrins; Arroyo Grande and McKittrick (California) have roughly equal amounts of both types; and Surmyside (Utah) has virtually none of either.

Size characteristic profiles (SEC-ICP) were generated for the extracted bitumens. The profiles are generally bimodal in shape and resemble several different specific heavy crude oils and residua. For examples, Arroyo Grande and McKittrick appear to be similar to Kern River (California) 650°F+ residuum, while Athabasca resembles Morichal (Venezuela) 650°F+ residuum.     

EFFECT OF PREHYDROGENATION ON HYDROCONVERSION OF MAYA RESIDUUM,PART II: HYDROGEN INCORPORATION

ABSTRACT

Maya 650° F residuum (Maya AR) was prehydrogenated over a standard hydroprocessing catalyst. The 650°F residuum of this product lpar;HMaya ARrpar; and Maya AR were then separately hydroprocessed further at selected conditions. The products were examined by elemental, ¹H, and ¹³C NMR analyses to determine the how hydrogen was incorporated during processing.

For all processing steps, hydrogen was incorporated in capping fragments formed during cracking reactions, as well as in hydrogenation reactions, heteroatom removal, and hydrocarbon gas formation, but the distribution of the hydrogen was dependent upon the type and severity of the process: For the direct hydroconversion of Maya AR, 25 to 30% of the total hydrogen was incorporated for heteroatom removal and hydrocarbon gas formation. The remaining hydrogen was incorporated in hydrogenation and cracking reactions.

For the two-step hydroconversion process, 30 to 40% of the total hydrogen was incorporated for heteroatom removal and hydrocarbon gas formation. The remaining was primarily incorporated in hydrogenation reactions. Some was incorporated into cracking reactions in the moderate severity case, but almost none was seen in the low severity case.

The hydrogen incorporation during each specific processing step is discussed, along with an evaluation of the prehydrogenation step a residuum conversion process option. These results will be also compared to previously reported hydrogen incorporation measurements on other feeds and processing methods.