Dynamic finite element simulation of the gunshot injury to the human forehead protected by polyvinyl alcohol sponge

Although there are some traditional models of the gunshot wounds, there is still a need for more modeling analyses due to the difficulties related to the gunshot wounds to the forehead region of the human skull. In this study, the degree of damage as a consequence of penetrating head injuries due to gunshot wounds was determined using a preliminary finite element (FE) model of the human skull. In addition, the role of polyvinyl alcohol (PVA) sponge, which can be used as an alternative to reinforce the kinetic energy absorption capacity of bulletproof vest and helmet materials, to minimize the amount of skull injury due to penetrating processes was investigated through the FE model. Digital computed tomography along with magnetic resonance imaging data of the human head were employed to launch a three-dimensional (3D) FE model of the skull. Two geometrical shapes of projectiles (steel ball and bullet) were simulated for penetrating with an initial impact velocity of 734 m/s using nonlinear dynamic modeling code, namely LS-DYNA. The role of the damaged/distorted elements were removed during computation when the stress or strain reached their thresholds. The stress distributions in various parts of the forehead and sponge after injury were also computed. The results revealed the same amount of stress for both the steel ball and bullet after hitting the skull. The modeling results also indicated the time that steel ball takes to penetrate into the skull is lower than that of the bullet. In addition, more than 21 % of the steel ball’s kinetic energy was absorbed by the PVA sponge and, subsequently, injury sternness of the forehead was considerably minimized. The findings advise the application of the PVA sponge as a substitute strengthening material to be able to diminish the energy of impact as well as the load transmitted to the object.     

A shortcut method for the preliminary synthesis of process-technology pathways: An optimization approach and application for the conceptual design of integrated biorefineries

Synthesis and screening of technology alternatives is a key process-development activity in the process industries. Recently, this has become particularly important for the conceptual design of biorefineries. This work introduces a shortcut method for the synthesis and screening of integrated biorefineries. A structural representation (referred to as the chemical species/conversion operator) is introduced. It is used to track individual chemicals while allowing for the processing of multiple chemicals in processing technologies. The representation is used to embed potential configurations of interest. An optimization approach is developed to screen and determine optimum network configurations for various technology pathways using simple data. The solution to the optimization formulation provides a quick and effective method for screening and interconnecting the technological pathways and to distributing the flows over the network. Case studies are solved to illustrate the applicability of the proposed approach.     

Studies of carbonaceous species in alkali promoted iron catalysts during Fischer–Tropsch synthesis

The effects of La, Mg and Ca promoters on carbonaceous surface and bulk iron carbide species formed in the alkali promoted iron catalysts are studied under realistic Fischer–Tropsch synthesis (FTS) conditions. Compositions of bulk iron phase and phase transformations of carbonaceous species during pretreatment and FTS reaction were characterized using the temperature-programmed surface reaction with hydrogen (TPSR-H₂) and XRD techniques. Many carbonaceous species on surface and bulk were qualitatively and quantitatively identified by combined TPSR-H₂ and XRD spectra of the alkali promoted iron catalyst. These species, sorted by the their reactivity with H₂ from high to low, were recognized as (a) adsorbed, atomic carbon; (b) amorphous, lightly polymerized hydrocarbon or carbon surface species; (c) bulk carbides and (d) disordered and moderately ordered graphitic surface carbons. The results revealed that while the surface basicity of the iron catalyst increased the CO dissociation proceeds faster than carbon hydrogenation. This phenomenon leads to excessive carbon deposition and formation of inactive iron carbide phases and graphitic type carbonaceous surface species, and consequently leads to catalyst deactivation.