An Algorithm for Computing Screened Coulomb Scattering in Geant4

An algorithm has been developed for the Geant4 Monte-Carlo package for the efficient computation of screened Coulomb interatomic scattering. It explicitly integrates the classical equations of motion for scattering events, resulting in precise tracking of both the projectile and the recoil target nucleus. The algorithm permits the user to plug in an arbitrary screening function, such as Lens-Jensen screening, which is good for backscattering calculations, or Ziegler-Biersack-Littmark screening, which is good for nuclear straggling and implantation problems. This will allow many of the applications of the TRIM and SRIM codes to be extended into the much more general Geant4 framework where nuclear and other effects can be included.Comment: 19 pages, 6 figures; corrected to rerferee comments, typo in equation 5 fixe

Modification of kraft wood-pulp fibre with silica for surface functionalisation

A new science strategy for natural fibre modification was devised in which glass surface properties would be imparted to wood-derived fibre. The enhancements known from addition of silane reagents to glass fibre–polymer composites could therefore be realised for modified cellulose fibre–polymer composites. A process is described whereby the internal void spaces and micropores of never-dried Kraft pulp fibre walls were impregnated with silica. This was achieved by initial dehydration of never-dried fibre through azeotropic distillation to achieve substitution of fibre water with the silicon chemical solution over a range of concentrations. Kraft fibres were stiffened and made resistant to collapse from the effect of the azeotrope drying. Specific chemical reaction of azeotrope-dried fibre with the reagent ClSi(OEt)3 followed by base-catalysed hydrolysis of the ester groups formed a fibre-bound silica composite. The physico-chemical substitution of water from micropores and internal voids of never-dried fibre with property-modifying chemicals offers possibilities in the development of new fibre characteristics, including fibres which may be hardened, plasticised, and/or stabilised against moisture, biodegradation or fire. The embedded silica may also be used as sites of attachment for coupling agents to modify the hydrophilic character of the fibre or to functionalise the fibre surface

The effect of silane coupling agents on radiata pine fibre for use in thermoplastic matrix composites

Gamma aminopropyltriethoxysilane (GS) and dichlorodiethylsilane (DCS) were employed for surface modification of radiata pine (Pinus radiata) wood fibre. Levels of fibre moisture were carefully controlled to optimise chemical and hydrogen bonding with these silane coupling agents. The effect of pre-treatment using 2% sodium hydroxide, shown to be effective in assisting silane coupling for other natural fibres [1], was also investigated. X-ray Photoelectron Spectroscopy (XPS) and Nuclear Magnetic Resonance (NMR) were used to characterise modification of the wood fibre. Concentrations of up to 3.2wt% Si were obtained on the fibre surface due to silane coupling, however, pre-treatment was found to dramatically reduce this value. NMR provided evidence that coupling had occurred between the fibre and DCS by a reaction producing ether linkages between the hydroxyl groups on the wood fibre and silane. Pre-treatment and treatment were found to have an insignificant effect on fibre strength. Composite sheets were produced by blending fibre (5, 10 and 20wt%) with polyethylene followed by extrusion. An increase in strength was obtained at fibre contents of 5wt% for all treatments compared to composites with untreated fibre. This is believed to be mainly due to increased compatibility of the fibre surface to polyethylene. However, there was no such improvement obtained at higher fibre contents. Evidence suggests that the production of voids is limiting composite strength

Dewatering Green Sapwood Using Carbon Dioxide Undergoing Cyclical Phase Change between Supercritical Fluid and Gas

Conventional kiln drying of wood operates by the evaporation of water at elevated temperature. In the initial stage of drying, mobile water in the wood cell lumen evaporates. More slowly, water bound in the wood cell walls evaporates, requiring the breaking of hydrogen bonds between water molecules and cellulose and hemicellulose polymers in the cell wall. An alternative for wood kiln drying is a patented process for green wood dewatering through the molecular interaction of supercritical carbon dioxide with water of wood cell sap. When the system pressure is reduced to below the critical point, phase change from supercritical fluid to gas occurs with a consequent large change in CO2 volume. This results in the efficient, rapid, mechanical expulsion of liquid sap from wood. The end-point of this cyclical phase-change process is wood dewatered to the cell wall fibre saturation point. This paper describes dewatering over a range of green wood specimen sizes, from laboratory physical chemistry studies to pilot-plant trials. Magnetic resonance imaging and nuclear magnetic resonance spectroscopy were applied to study the fundamental mechanisms of the process, which were contrasted with similar studies of conventional thermal wood drying. In conclusion, opportunities and impediments towards the commercialisation of the green wood dewatering process are discussed