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abstract: Ultra-concealable multi-threat body armor used by law-enforcement is a multi-purpose armor that protects against attacks from knife, spikes, and small caliber rounds. The design of this type of armor involves fiber-resin composite materials that are flexible, light, are not unduly affected by environmental conditions, and perform as required. The National Institute of Justice (NIJ) characterizes this type of armor as low-level protection armor. NIJ also specifies the geometry of the knife and spike as well as the strike energy levels required for this level of protection. The biggest challenges are to design a thin, lightweight and ultra-concealable armor that can be worn under street clothes. In this study, several fundamental tasks involved in the design of such armor are addressed. First, the roles of design of experiments and regression analysis in experimental testing and finite element analysis are presented. Second, off-the-shelf materials available from international material manufacturers are characterized via laboratory experiments. Third, the calibration process required for a constitutive model is explained through the use of experimental data and computer software. Various material models in LS-DYNA for use in the finite element model are discussed. Numerical results are generated via finite element simulations and are compared against experimental data thus establishing the foundation for optimizing the design. / Dissertation/Thesis / M.S. Civil and Environmental Engineering 2012

A demanda por qualidade nas aplicações envolvendo radiação laser exigiu melhorias no seu desempenho. Conseqüentemente, equipamentos mais rápidos e precisos nas medidas dos seus parâmetros são indispensáveis. Nas áreas onde o laser é empregado, três parâmetros sobressaem-se nas suas aplicações: (1) potência ou energia, (2) freqüência e (3) comprimento espacial ou largura do feixe. A determinação das bordas, isto é, da largura do feixe, está ligada a um percentual do máximo valor atingido pela energia. O diâmetro do feixe, juntamente com a energia, determina-se a densidade do feixe. Outros parâmetros como: divergência e fator de qualidade (M2), podem ser determinados também. O presente trabalho busca desenvolver um sistema de translação bidimensional que possa ser empregado na caracterização espacial do feixe de lasers. Para determinar o perfil do feixe de lasers utiliza-se o método borda-da-lâmina (knife-edge), relacionando o deslocamento da lâmina posicionada transversalmente ao feixe, com a energia transmitida. Obstruindo o feixe com uma lâmina opaca, obtêm-se a variação da energia do feixe em função da posição da lâmina. Esta variação representa a integral do perfil Gaussiano do feixe. Para a automação do sistema foi empregado o programa Labview (National Instruments). O funcionamento do protótipo mostrou-se eficiente na caracterização de feixes laser e com uma instrumentação de baixo custo para a comercialização nacional. No entanto, apresentou-se lento na aquisição de dados, tornando a tarefa de caracterização do laser mais demorada. Fatores como velocidade do motor de passo e linguagem de programação contribuíram para tornar a aquisição lenta. / The demand for quality in the applications involving laser radiation demanded improvements in its performance. Faster equipments in the measures of its parameters are indispensable. In the areas where the laser is employee, three parameters are important in its applications: (1) power or energy, (2) frequency and (3) beam spatial. The determination of the edges, i. e., the width of the beam, is correlated to a percentage of the maximum reached energy. This parameter, together with the energy, determines beam density; beyond this parameter it also possible to determine the divergence and quality factor (M2). This work searches to develop a system of bi-dimension translation that can be used in the spatial characterization of laser beam. To determine the profile of laser beam it is used the knife-edge method, that it relates the displacement of the blade located transversally to the beam, with the transmitted energy. Blocking the beam with a blade the energy variation of the beam is correlated with blade position; this variation represents the integral of the beam Gaussian profile. For the automation it will be used the Labview program(National Instruments). The prototype had showed to be efficient in the characterization of laser beams and a low cost for national commercialization; however was slow in the data acquisition resulting a longer time to acquire the laser parameters. Instrumental components as step motors or programming language had contributed to slowly acquisition.

BACKGROUND: Piezoelectric surgery (PIEZO) uses ultrasonic vibration to cut hard tissue without damaging adjacent soft tissues. Our previous studies indicated that PIEZO enhanced bone turnover compared to a conventional rotary bur (BUR) in rat tibia wounds by inducing the regional acceleratory phenomenon (RAP). PIEZO induced osteocyte apoptosis without damaging blood vessels during Day 1, 3 and 7 of rat tibia healing. We hypothesized that PIEZO increased bone turnover by activation of osteocyte apoptosis with a controlled inflammatory response. This study evaluated early morphological changes in tibial defects caused by either PIEZO or BUR. MATERIALS & METHODS: We created surgical defects in tibia by either PIEZO or BUR in 9–10-week-old Sprague-Dawley rat tibias (n=4). We evaluated tissue responses by using H&E, Masson’s Trichrome and TRAP stains on Day 1, 3 & 7 after surgery. The surgical defect beneath the soft tissue was located using Computed Tomography (CT). RESULTS: On postoperative Day 1, there was no significant blood vessel change or cellular extravasation in the PIEZO group. In contrast the BUR group had extravasation of leukocytes and increased blood vessels' size. On Day3, there was no significant inflammation or morphological changes to blood vessels in the PIEZO group. Empty lacunae adjacent to the defect area suggested osteocyte apoptosis. In the BUR group, blood vessels returned to an average size and the leukocyte population was reduced and bone adjacent to the lesion was unaffected, and intact osteocytes were in the lacunae. On Day 7 there was increased in osteoclastic activity in Piezo compared the BUR group. CONCLUSION: These results suggested that PIEZO induced osteocyte apoptosis, increased bone turnover with a controlled inflammatory response and protected the bone blood vessel network.

This thesis presents the development and evaluation of the knife finite element which is a degenerate case of a hexahedral element. The knife connectivity is an artifact of automatic all-hexahedral mesh generators. Currently, knives are propagated to the surface of the mesh for removal. However since this disturbs the surface mesh, other alternatives are needed. This thesis investigates the option of leaving the knife connectivity in the mesh and treating it as a valid finite element. The shape functions and stiffness matrix for the knife element are derived and evaluated using theoretical and practical evaluations. It is concluded that the knife finite element is a viable element and should be used in finite element analysis when the knife connectivity occurs. Using the knife element reduces the work involved with fixing the knife connectivity by propagation or other means and will produce acceptable results in most cases.

A radiocirurgia estereotáxica é um procedimento que trata principalmente lesões intracranianas para destruir células tumorais inacessíveis cirurgicamente. O Gamma Knife® é uma unidade de radiocirurgia estereotáxica que trata lesões exclusivamente cerebrais com feixes de 60Co de forma não-invasiva. De forma a garantir a acurácia na entrega da dose, esse tipo de equipamento necessita de detectores adequados para determinar a dose a ser entregue com exatidão. O protocolo da IAEA, TRS 483, é um guia padronizado para procedimentos dosimétricos e indicação de detectores relativos à dosimetria de referência de campos pequenos usados em feixes de radioterapia. Este trabalho seguiu as recomendações do TRS 483 na dosimetria do Gamma Knife® e foram realizadas medições utilizando duas câmaras de ionização, Exradin A16 e PTW Pinpoint 3D 31016, a alanina como detector de referência e os objetos simuladores indicados pela Elekta, fabricante do Gamma Knife®, sendo um de ABS e outro de Solid Water®. Um objeto simulador de acrílico foi construído, com as mesmas dimensões dos indicados pela Elekta, e implementado na dosimetria de equipamentos Gamma Knife®. A calibração das câmaras de ionização utilizadas foi realizada em um laboratório padrão primário e o coeficiente de calibração obtido foi utilizado no cálculo da dose absorvida na água dessas câmaras. Os estudos e testes dosimétricos realizados com o objeto simulador construído demonstraram resultados próximos aos simuladores existentes. Todos os fatores de correção indicados pelo TRS 483 foram considerados para o cálculo da dose absorvida. Foi constatado que o novo objeto simulador pode ser utilizado na dosimetria de Gamma Knife® e também para calibração de câmaras de ionização de volume pequeno, garantindo uma configuração de dosimetria e calibração similares e proporcionando ao usuário uma calibração próxima à configuração da dosimetria clínica. O projeto e a execução do objeto simulador utilizado neste trabalho visa contribuir para o TRS 483, de forma que seja utilizado na aplicação da dosimetria de Gamma Knife® e na calibração de câmaras de ionização de volume pequeno. / Stereotactic radiosurgery is a procedure that primarily treats intracranial lesions to destroy tumor cells that are inaccessible surgically. Gamma Knife® is a stereotactic radiosurgery unit that treats exclusively cerebral lesions using 60Co beams non-invasively. In order to ensure accurate dose delivery, this type of equipment requires adequate detectors to determine the dose is delivered accurately. The IAEA TRS 483 protocol is a standardized guide for dosimetric procedures and indication of detectors for reference dosimetry of small fields used in radiotherapy beams. Following TRS 483 recommendations in Gamma Knife® dosimetry, the measurements performed in this work used two ionization chambers; Exradin A16 and PTW Pinpoint 3D 31016, alanine as reference detector and phantoms indicated by Elekta, Gamma Knife\'s® manufacturer, which are made of ABS and Solid Water®. An acrylic phantom was built with the same dimensions as those indicated by Elekta, and implemented for the Gamma Knife® dosimetry. The calibration of the ionization chambers used was performed in a primary standard laboratory and the calibration coefficient obtained was used to calculate the absorbed dose in the water for these chambers. The dosimetry and tests performed with the acrylic phantom showed results close to the existing phantoms. All the correction factors indicated by TRS 483 were considered for the absorbed dose to water calculation. The new phantom can be used in Gamma Knife® dosimetry and also for calibration of small volume ionization chambers, assuring a similar dosimetry and calibration configuration and providing a calibration close to the clinical dosimetry configuration for the user. The design and implementation of the simulator object used in this work aims to contribute to the TRS 483, for the use in Gamma Knife® dosimetry and in the calibration of small volume ionization chambers.

A radiocirurgia estereotáxica é um procedimento que trata principalmente lesões intracranianas para destruir células tumorais inacessíveis cirurgicamente. O Gamma Knife® é uma unidade de radiocirurgia estereotáxica que trata lesões exclusivamente cerebrais com feixes de 60Co de forma não-invasiva. De forma a garantir a acurácia na entrega da dose, esse tipo de equipamento necessita de detectores adequados para determinar a dose a ser entregue com exatidão. O protocolo da IAEA, TRS 483, é um guia padronizado para procedimentos dosimétricos e indicação de detectores relativos à dosimetria de referência de campos pequenos usados em feixes de radioterapia. Este trabalho seguiu as recomendações do TRS 483 na dosimetria do Gamma Knife® e foram realizadas medições utilizando duas câmaras de ionização, Exradin A16 e PTW Pinpoint 3D 31016, a alanina como detector de referência e os objetos simuladores indicados pela Elekta, fabricante do Gamma Knife®, sendo um de ABS e outro de Solid Water®. Um objeto simulador de acrílico foi construído, com as mesmas dimensões dos indicados pela Elekta, e implementado na dosimetria de equipamentos Gamma Knife®. A calibração das câmaras de ionização utilizadas foi realizada em um laboratório padrão primário e o coeficiente de calibração obtido foi utilizado no cálculo da dose absorvida na água dessas câmaras. Os estudos e testes dosimétricos realizados com o objeto simulador construído demonstraram resultados próximos aos simuladores existentes. Todos os fatores de correção indicados pelo TRS 483 foram considerados para o cálculo da dose absorvida. Foi constatado que o novo objeto simulador pode ser utilizado na dosimetria de Gamma Knife® e também para calibração de câmaras de ionização de volume pequeno, garantindo uma configuração de dosimetria e calibração similares e proporcionando ao usuário uma calibração próxima à configuração da dosimetria clínica. O projeto e a execução do objeto simulador utilizado neste trabalho visa contribuir para o TRS 483, de forma que seja utilizado na aplicação da dosimetria de Gamma Knife® e na calibração de câmaras de ionização de volume pequeno. / Stereotactic radiosurgery is a procedure that primarily treats intracranial lesions to destroy tumor cells that are inaccessible surgically. Gamma Knife® is a stereotactic radiosurgery unit that treats exclusively cerebral lesions using 60Co beams non-invasively. In order to ensure accurate dose delivery, this type of equipment requires adequate detectors to determine the dose is delivered accurately. The IAEA TRS 483 protocol is a standardized guide for dosimetric procedures and indication of detectors for reference dosimetry of small fields used in radiotherapy beams. Following TRS 483 recommendations in Gamma Knife® dosimetry, the measurements performed in this work used two ionization chambers; Exradin A16 and PTW Pinpoint 3D 31016, alanine as reference detector and phantoms indicated by Elekta, Gamma Knife\'s® manufacturer, which are made of ABS and Solid Water®. An acrylic phantom was built with the same dimensions as those indicated by Elekta, and implemented for the Gamma Knife® dosimetry. The calibration of the ionization chambers used was performed in a primary standard laboratory and the calibration coefficient obtained was used to calculate the absorbed dose in the water for these chambers. The dosimetry and tests performed with the acrylic phantom showed results close to the existing phantoms. All the correction factors indicated by TRS 483 were considered for the absorbed dose to water calculation. The new phantom can be used in Gamma Knife® dosimetry and also for calibration of small volume ionization chambers, assuring a similar dosimetry and calibration configuration and providing a calibration close to the clinical dosimetry configuration for the user. The design and implementation of the simulator object used in this work aims to contribute to the TRS 483, for the use in Gamma Knife® dosimetry and in the calibration of small volume ionization chambers.

Recycling of plastics always plays an important role in keeping our environment better and safe. With the rise in usage of plastics and industrialization, the need for recycling the plastics has become a big business and is getting bigger. This thesis work was done for a company called Rapid Granulator AB, which works with the recycling of plastics as a big trade in Sweden. Like all the industries across the globe are trying to be economical in every way, Rapid Granulator AB wanted to develop an economical design of their high quality granulating knife. For achieving the economical design, they wanted to study the behaviour of the rotating knife during the process of producing plastic granules. The granulator cutting process was simulated and numerical analysis was done on the rotating knife of a plastic granulator machine by using the finite element code ABAQUS with 3D stress elements to find out the critical stresses and forces acting on the rotating knife. The bolt preload was applied by Abaqus/Standard, and the results of implicit analysis were imported to Abaqus/Explicit for the impact analysis where the flow of stresses on the rotating knife during the impact with materials were simulated and studied. The study was done on knife models of different thickness to see if the thickness of the current knife model can be reduced. Analysis were done also on a knife model assembly with a double sided cutting edge knife to see if the knife model can be used to its full extent. The simulation models and analysis results were given to the company to develop a more economical knife model.

The interest in environmental issues is increasing and for this reason, assessing the potential environmental impacts of a product or system is of interest. A methodology developed for this particular purpose is the life cycle assessment, also known as LCA. It is not purely of interest these aspects are investigated though, as increasing requirements on organizations also matter. The purpose of this thesis was to investigate the feasibility to implement the methodology of LCA in the aspect of complex medical devices. To do this, the framework for the methodology has been reviewed and a case study performed. The case study comprised of conducting an LCA study on the radiosurgery device Leksell Gamma Knife® IconTM.  The outcome of the investigation showed that conducting an LCA study means a wide range of aspects need to be considered and specified to a high degree. A particular issue was the data requirements, as obtaining data meeting several objectives was challenging. The modeling was also identified as a difficulty. Tools such as software and databases with predefined processes were used, though as complex medical devices can use materials not common in other fields, a lack of appropriate predefined processes hinders the feasibility. The conducted case study was able to attain valuable insights even though the study did not comply with the standards providing the framework, the ISO 14040 series. To conduct a compliant LCA study for complex medical devices, extensive resources would be required as well as the involvement of relevant parties along the supply chain. It is seen improbable to achieve a compliant study the first time a particular type of complex medical device is investigated. However, it is believed the feasibility would increase as studies are repeated, as the data quality is likely to increase. Advancements of the tools, as well as ongoing research on the environmental impacts of more materials, are other factors thought to increase the feasibility of conducting LCA studies on complex medical devices in the future. / Intresset för miljöfrågor ökar och därav finns det ett intresse att undersöka vad den potentiella miljöpåverkan är för en produkt eller ett system. En metodologi utvecklad för detta specifika syfte är livscykelanalys som även kallas LCA. Det är inte enbart utav intresse som aspekterna utreds, de ökande krav som ställs på olika aktörer spelar också roll. Syftet med detta examensarbete var att undersöka genomförbarheten av livscykelanalyser med avseende på komplexa medicintekniska produkter. Detta gjordes genom att granska regelverken för LCA samt genomförandet av en fallstudie, vilken utgjordes av en livscykelanalys på strålkniven Leksell Gamma Knife® IconTM. Resultaten av undersökningen visade att genomförandet av en livscykelanalys innebär att ett stort spann av aspekter måste beaktas och specificeras i hög grad. Ett särskilt problem var kraven på data då det var utmanande att samla in data som skulle möta flera behov. En annan identifierad svårighet var modelleringen. Verktyg användes i form av mjukvara och databaser med fördefinierade processer men då komplexa medicintekniska produkter kan bestå av material som inte är vanliga inom andra områden, var bristen på passande fördefinierade processer ett hinder för genomförbarheten. Den genomförda fallstudien gav värdefulla resultat trots att den inte var utförd helt enligt standarderna i ISO 14040 serien. För att en LCA studie för komplexa medicintekniska produkter skall möta dessa krav krävs omfattande resurser och att flera berörda parter längs försörjningskedjan involveras. Det ses därför som osannolikt att en studie som genomförs för första gången på en viss typ av komplex medicinteknisk produkt kan leva upp till regelverket. Dock så förmodas genomförbarheten öka i takt med att studier upprepas, då kvaliteten på data tros öka. Utveckling av verktygen samt pågående forskning om miljöpåverkan från olika material är andra faktorer som anses öka genomförbarheten av livscykelanalyser på komplexa medicintekniska produkter i framtiden.