Dissertations / Theses on the topic 'Engineering preparation'

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1

Whiteley, Clinton E. "Emergency Preparation and Green Engineering Tool." Thesis, Manhattan, Kan. : Kansas State University, 2008. http://hdl.handle.net/2097/551.

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2

Zhang, Rongsheng. "Dextran hydrogel preparation and applications in biomedical engineering." Thesis, University of Bath, 2004. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.398371.

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3

DeBiase, Kirstie. "Teacher preparation in science, technology, engineering, and mathematics instruction." Thesis, California State University, Long Beach, 2016. http://pqdtopen.proquest.com/#viewpdf?dispub=10118901.

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The purpose of this qualitative case study was to gain a better understanding of how induction programs might effectively support STEM K?8 teacher preparation. American schools are not producing competent STEM graduates prepared to meet employment demands. Over the next decade, STEM employment opportunities are expected to increase twice as fast as all other occupations combined. To meet the economic needs, the STEM pipeline must be expanded to educate and produce additional STEM graduates. The meeting of this objective begins with having the teachers working in American classrooms fully prepared and trained in STEM content, curriculum, and pedagogy. Research shows that the interest in STEM subjects starts in elementary school and, therefore, the preparation of elementary teachers to be proficient in teaching STEM to their students is vital. However, most induction programs do not focus on preparing their teachers in STEM. This study researched the Alternative Induction Pathway (AIP) program, which had STEM preparation as one of its core outcomes in the Long Beach Unified School District (LBUSD). It investigated the program?s effectiveness in preparing K?8 teachers with STEM content knowledge, curriculum, pedagogical instruction preparation, and the program elements that contributed the most to their experience in the program and overall STEM preparation as a result. This study was carried out over the course of approximately 6 months. Data included focused interviews with participants as well as analysis of existing documents in order to triangulate perspectives from multiple sources. The AIP program had varied levels of effectiveness in STEM content, curriculum, and pedagogy preparation. Relationships between the induction mentor, the administration, and the participating teacher, when strong and positive, were powerful contributions to the success of the acquisition and integration of the STEM content, curriculum, and pedagogy. The most effective components of the AIP program were the monthly support groups, the curricular resources, and the professional development nights facilitating the teaching and learning process for the participating teacher in STEM integration. The results of this training included examples of well-planned and executed STEM lessons with creative risk-taking, and enhanced confidence for teachers and administrators alike. At the same time, the AIP program had struggles in achieving the desired outcomes of STEM integration, due to lack of preliminary training for program administrators in STEM integration, varied needs between the MS and SS credential teachers, and state standard requirements that spoke to science and mathematics, but not engineering or technology. The main recommendation for policy from the results of this study is that STEM should be woven into preservice and continue through induction and professional development to become one of the main tenets of curriculum development and standards of effective teaching. This policy would affect colleges of education and district induction programs, requiring that STEM courses be added or embedded into the credential pathways. However, this approach would ensure that STEM integration is supported academically as an important and valued aspect of the teacher?s entrance to their career, and that pre-service teachers are ready to take advantage of induction offerings on STEM integration in the induction phase and throughout their careers in continuing professional development. The study also provides practice and research recommendations in regard to possible roles and supports for mentor teachers, including their relationships with resident teachers, as well as suggestions for and to maximize the benefits for effective teaching and learning during the induction process.

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4

Erasmus, Willem Johannes. "Preparation of model cobalt catalysts for Fischer-Tropsch synthesis using ultrasound preparation techniques." Master's thesis, University of Cape Town, 2006. http://hdl.handle.net/11427/5335.

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Includes bibliographical references (leaves 84-87).
In order to study the oxidation behaviour of small cobalt crystallites during Fischer-Tropsch synthesis, it is necessary to prepare model catalysts with cobalt crystallites of which the size distributions can be adjusted. Here ultrasonication was used to decomposed a tricarbonyl precursor in n-decane to prepare small cobalt crystallites. The aim of this study was to vary the cobalt crystallite size distribution by adjusting the preparation conditions. Transmission Electron Microscopy (TEM) was used to measure the crystallites and to obtain the crystallite size distributions.
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5

Waterbury, Raymond. "The electron microscopy proteomic organellar preparation robot /." Thesis, McGill University, 2006. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=102768.

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An Electron Microscopy Proteomic Organellar Preparation (EMPOP) robot was developed as a tool for high-throughput preparation of subcellular fraction samples for electron microscopic identification. It will provide a means for validation of subcellular sample purity and confirmation of protein localization needed for organellar proteomics.
The device automates all chemical and mechanical manipulations required to prepare organelles for electron microscopic examination. It has a modular, integrated design that supports automated filtration, chemical processing, delivery and embedding of up to 96 subcellular fraction samples in parallel. Subcellular fraction specimens are extremely fragile. Consequently, the system was designed as a single unit to minimize mechanical stress on the samples by integrating a core mechanism, composed of four modular plates, and seven support subsystems for: (1) cooling, (2-3) fluid handling, (4-7) positioning. Furthermore, control software was developed specifically for the system to provide standardized, reproducible sample processing while maintaining flexibility for adjustment and recall of operational parameters.
Development of the automated process progressed from initial validation experiments and process screening to define operational parameters for preservation of sample integrity and establish a basic starting point for successful sample preparation. A series of successive modifications to seal the local environment of the samples and minimize the effect of fluidic perturbations further increased process performance. Subsequent testing of the robot's full sample preparation capacity used these refinements to generate 96 samples in approximately 16 hours; reducing the time and labor requirement of equivalent manual preparation by up to 1,000 fold.
These results provide a basis for a structured approach toward process optimization and subsequent utilization the device for massive, parallel preparation of subcellular fraction samples for electron microscopic screening and quantitative analysis of subcellular and protein targets necessary for high-throughput proteomics.
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6

Zhang, Huan Ph D. Massachusetts Institute of Technology. "Preparation and applications of catalytic magnetic nanoparticles." Thesis, Massachusetts Institute of Technology, 2008. http://hdl.handle.net/1721.1/46672.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemical Engineering, 2009.
Includes bibliographical references.
It is critical to decontaminate organophosphate compounds in large scale economically, including OP pesticides in groundwater system and chemical nerve agents on the battle field. Homogeneous or micellar decomposition systems with various nucleophiles improve reaction rates significantly without affording the recovery and reuse of the nucleophiles. This research focuses on developing functional magnetic particles to carry strong [alpha]--nucleophilic groups, which are able to catalyze the decomposition reaction and can be recycled and reused.The amidoxime modified magnetic particles were prepared first. The original particles were synthesized with the two-step procedure to obtain average particle size of around 80nm for effective capture by high gradient magnetic separation (HGMS). The precursor molecule cyanoacetohydrazide reacted with the free carboxyl groups on the particle surfaces and subsequently the nitrile groups were transformed into amidoxime groups. The modified particles were of similar average hydrodynamic diameter as the original ones and colloidally stable over a wide range of solutin pH. The amidoxime-modified particles accelerated the hydrolysis reaction of p-nitrophenyl acetate (PNPA). They were easily recycled by HGMS without loss of reactivity. Higher reactivity of the particle system than homogenous amidoxime systems was attributed to the increased concentration of the substrate on the particle surface due to the presence of hydrophobic centers using pseudo-phase exchange model.Stronger nucleophilic groups, hydroxamic acid, were then attached on the particle surfaces. Original particles were prepared with unsaturated carboxylic acid as the second coating in the two-step procedure. The acrylamide monomers were copolymerized with the second coating and the attached amide groups were converted into the hydroxamic acid groups.
(cont.) The reaction was very efficient. Crosslinking increased the particle size to 200nm and therefore the particles were effectively captured by HGMS. The modified particles significantly accelerated the hydrolysis reaction of PNPA. They were five times more reactive than the amidoxime modified particles based on the same weight of materials. The acetylated particles were only partially regenerated due to the Lossen rearrangement of the acetylated hydroxamic acid groups.During the hydrolysis of OP substrates, including diisopropyl fluorophosphate, methylparaoxon and ethyl-paraoxon, the added a-nucleophiles, 2-PAM and acetohydroxamic acid, only attacked the phosphorus atom to substitute the p-nitrophenol groups in methyland ethyl- paraoxon and the fluoride ions in DFP through second order nucleophilic substitution. Reactions between all three substrates and both nucleophiles yielded the same hydrolysis products as the spontaneous hydrolysis with no detected intermediates, indicating the unstable nature of any intermediates that may be formed. The hydroxamic acid modified particles accelerated the hydrolysis of methyl- and ethyl- paraoxon with relatively modest reactivity. Similar to polyhydroxamic acid, the reactivity was much lower than that of monomeric hydroxamic acid due to the steric hindrance from the polymer chains. The particles lost their reactivity after the reaction due to Lossen rearrangement of the phosphoryl hydroxamic acid.
by Huan Zhang.
Ph.D.
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7

Hill, Matthew Raymond. "Preparation of catalyst coated membranes using screen printing." Master's thesis, University of Cape Town, 2013. http://hdl.handle.net/11427/11834.

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Of the various types of fuel cells, Polymer Electrolyte Fuel Cells (PEFCs) have already been demonstrated in transportation appliances from light-duty vehicles to buses and in portable appliances including laptops and cell phones. A key component of a PEFC is its platinum electrocatalyst. With an estimated 75% of the world’s platinum reserves and resources in South Africa, local development of this technology will allow South Africa to become a major player in the growing hydrogen economy. This project therefore forms part of the Department of Science and Technologies strategy, to develop fuel cell technology in South Africa. More specifically, this study aims to contribute to the development of membrane electrode assembly (MEA) platform technology at the HySA/Catalysis Centre. In order to achieve this goal, a catalyst coated membrane (CCM) fabrication procedure was implemented using a newly acquired screen printer. In this procedure, catalyst ink is forced through a mesh onto a substrate, where it can then be transferred to a membrane via decal transfer to form a CCM. Two gas diffusions layers can then be placed on either side of the CCM forming a 5-layered MEA. Characterisation techniques of the catalyst ink, CCM and 5-layered MEA were successfully implemented such that future researchers can expand on the ideas. Catalyst inks with varying amounts of isopropanol, 1,2-propanediol and water were screened for their suitability for screen printing. In particular the catalyst ink rheology required for a smooth and even printed surface was determined for a given screen and squeegee combination. With all the established steps in pace, screen printing proved to be a fast and reliable approach for CCM fabrication with potential for future scale up and commercialisation. The fabricated CCMs performed on a par with a commercial Ion Power CCM, but under performed in comparison to a commercial Johnson Matthey (JM) MEA. Possible reasons for this include improved materials in the JM MEA and cell conditions favouring the JM MEA. Future projects which specifically arise from this work entail an investigation into the water management of the fuel cell environment at HySA/Catalysis, as well as a modification of the various steps in order to optimise the process and in doing so manufacture commercially viable MEAs.
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8

Hsu, Hung-Liang. "The preparation and characterisation of porous degradable chitosan structures for tissue engineering." Thesis, Queen Mary, University of London, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.528416.

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9

Tanahashi, Kazuhiro. "DESIGN AND PREPARATION OF FUMARATE-BASED BIODEGRADABLE POLYMER HYDROGELS FOR TISSUE ENGINEERING." 京都大学 (Kyoto University), 2009. http://hdl.handle.net/2433/124562.

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10

Hasson, Dhari A. "Mixture preparation and combustion in spark ignition engines." Thesis, Aston University, 1986. http://publications.aston.ac.uk/11867/.

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11

Fowell, Susan Lynne. "The preparation and properties of immunosorbents." Thesis, University of Cambridge, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.293817.

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12

Å, iÅ man Güvenç S. 1971. "Design of an automated fiber pigtail preparation machine." Thesis, Massachusetts Institute of Technology, 1997. http://hdl.handle.net/1721.1/9390.

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13

Newman, Philip. "The preparation and transportation of paste backfill /." Thesis, McGill University, 1992. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=61309.

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Paste backfill has recently emerged in the Canadian mining industry as a potential solution to some of the problems regarding the waste disposal of mine tailings. Surface disposal is costly and its potential harm to the environment is incalculable.
Besides waste disposal paste backfill also produces a stronger fill resulting in less dilution, less cement consumption and less clean up costs. These savings can only be realized with an accurate implementation of the new technology.
Presented is an overview of the current state of this emerging technology and the available equipment required for the preparation and transportation of paste backfill. It is hoped this work will provide the reader with a thorough grounding in paste backfill and enable him/her to understand that although large savings are possible the technology is still unproven within the context of the Canadian mining industry and further work is required before paste backfill becomes common practice.
Economic analyses are also presented regarding the different applications of paste at either existing or new mineral developments. Results from strength tests carried out as part of paste backfill feasibility projects are presented and show the increase in uniaxial compressive strength associated with an increase in slurry concentration. (Abstract shortened by UMI.)
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14

Cooper, J. D. H. "Automated sample preparation for high pressure liquid chromatography." Thesis, De Montfort University, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.292855.

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15

Isikli, Cansel. "Preparation And Characterization Of Chitosan-gelatin/hydroxyapatite Scaffolds For Hard Tissue Engineering Approaches." Master's thesis, METU, 2010. http://etd.lib.metu.edu.tr/upload/3/12611568/index.pdf.

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Hard tissue engineering holds the promise of restoring the function of failed hard tissues and involves growing specific cells on extracellular matrix (ECM) to develop &bdquo
&bdquo
tissue-like&rdquo
structures or organoids. Chitosan is a linear amino polysaccharide that can provide a convenient physical and biological environment in tissue regeneration attempt. To improve chitosan&
#8223
s mechanical and biological properties, it was blended with another polymer gelatin. 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDC) and N-hydroxysuccinimide (NHS) were used to crosslink the chitosan-gelatin matrix to produce stable structures. These natural polymers are mechanically weak especially to serve as a bone substitude and therefore, an inorganic calcium phosphate ceramic, hydroxyapatite, was incorporated to improve this aspect. The objective of this study was to develop chitosan-gelatin/hydroxyapatite scaffolds for a successful hard tissue engineering approach. For this reason, two types of hydroxyapatite, as-precipitated non-sintered (nsHA) and highly crystalline sintered (sHA) were synthesized and blended into mixtures of chitosan (C) and gelatin (G) v to produce 2-D (film) and 3-D (sponge) structures. The physicochemical properties of the structures were evaluated by scanning electron microscopy, X-Ray Diffraction (XRD), Fourier Transform Infrared-Attenuated Total Reflectance spectrometer (FTIR-ATR), differential scanning calorimetry, contact angle and surface free energy measurements and swelling tests. Mechanical properties were determined through tensile and compression tests. In vitro cell affinity studies were carried out with SaOs-2 cells. MTS assays were carried out to study cell attachment and proliferation on the 2-D and 3-D scaffolds. Several methods such as confocal, fluorescence and scanning electron microscopy were used to examine the cell response towards the scaffolds. Cell affinities of the samples were observed to change with changing chitosan-gelatin ratio and hydroxyapatite addition into the matrices. XRD and FTIR results confirmed the purity of the hydroxyapatite synthesized. Mechanical test results showed that 2-D and 3-D chitosan-gelatin/hydroxyapatite constructs have similar properties as bones, and in vitro studies demonstrated that the prepared matrices have the potential to serve as scaffold materials in hard tissue engineering applications.
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Walton, Robin S. "Preparation and analysis of type 1/type 11 collagens for tissue engineering scaffolds." Thesis, University of Oxford, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.540291.

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17

Balubaid, Eyad Khalid M. "Preparation and Characterization of Porous PDMS for Printed Electronics." Wright State University / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=wright1578073290398846.

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18

Qiu, Shuzhen. "Preparation and characterization of Matrimid/P84 blend films." Thesis, Kansas State University, 2014. http://hdl.handle.net/2097/18803.

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Master of Science
Department of Chemical Engineering
Mary Rezac
Polymeric membranes have been playing important roles in gas or liquid separations. Polyimide polymers are of interest due to their commercially availability along with good transport, thermal and mechanical properties. In this study, two common commercial polyimide polymers, Matrimid and P84 were blended, to combine the good transport property of Matrimid with the plasticization resistance of P84. Matrimid/P84 blend solutions ranging from 0-100 wt. % Matrimid were prepared to make blend films. Physical properties (density, d-spacing, thickness), transport properties (permeability of H2, N2, CH4, Ar, He, CO2, and gas pairs selectivity), thermal property (mass loss curves of TGA), and liquid solutes (water, methanol, toluene, butanol, 1-propanol, 2-propanol) desorption behavior were measured or characterized. Rules of changing behavior of the properties with mass fraction of Matrimid were investigated, summarized, and interpreted mathematically. As Matrimid mass fraction increases, there are more mobility and space between polymer chains, therefore there are smaller density, larger d-spacing, larger fractional free volume (FFV) and larger permeability. The selectivity-permeability relationship follows the trade-off line. Thermal mass loss curve of the blend films in air have presented intermediate characteristic with rising fraction of Matrimid compared to individual polymers. A partial-miscible behavior has been found from the correlation between permeability and FFV. The desorption behavior was found to be reasonably described by the case III model, where the diffusion rate is similar with relaxation rate of polymers.
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19

Haggarty, Allison. "Preparation and characterization of monoclonal antibodies against carcinoembryonic antigen." Thesis, McGill University, 1986. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=74041.

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20

Aguilar, Reyes Ena Athenea. "Preparation and characterization of rapid solidified yttria-alumina fibers." Thesis, McGill University, 2000. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=36860.

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A melt extraction process with a new approach to making ceramic fibers was used to produce amorphous fibers in the Y2O3-Al 2O3 system within the 20--30 micron size range. Three different compositions were studied, E1, Y3A5 and E2 with 79, 62.5 and 57.5 mol% Al2O3, respectively. Such fibers were X-ray amorphous and transparent, regardless of composition in the as-produced state, and showed all the principal characteristics of the fibers made by this process: a cross section which is almost circular, a line of contact with the wheel and a clean and defect-free surface. However, the quality of the fibers was controlled by the wheel edge and rotational speed, with both having a significant effect on fiber diameter and avoidance of irregularities and instabilities along the fiber length. Moreover, compositional distribution analysis showed that the melt-extracted fibers were chemically homogeneous between the core and the edge of the fiber and, in addition, were very close to theoretical stoichiometry.
Thermal analysis was performed in order to determine the glass transition, crystallization and phase transformation temperatures. E1 fibers showed two exothermic peaks at 949 and 1040°C that correspond to the crystallization of YAG and delta-Al2O3 phases, respectively, and one small exothermic peak at 1300°C due to the phase transformation of delta-Al 2O3 to alpha-Al2O3. In the case of Y3A5 and E2 fibers, both showed one single exothermic peak at 942 and 939°C due to the crystallization of YAG and YAP cubic phases, respectively. YAP orthorhombic and YAG phases appeared in E2 fibers after heat-treating at 1400°C for 1h with no identifiable exothermic peak in the DTA scan.
Differential thermal analysis was used to study the crystallization phenomena in the as-extracted fibers. The activation energy values were calculated using both Kissinger and Augis-Bennett equations by measuring the variation of the peak temperature in the differential thermal scans with heating rate, and the crystallization mode was identified using the Ozawa analysis. After crystallization, there was a conversion of the transparent glass fiber to an opaque polycrystalline material and both E1 and Y3A5 fibers had a nanocrystalline microstructure with a grain size typically of 100--500 nm. In the case of E2, the grain size was 1--2 mum.
Tensile strengths and elastic moduli of the fibers in the glassy state varied from 606 to 776 MPa and from 95 to 121 GPa, respectively. Furthermore, fibers exhibited brittle fracture initiated from flaws on the fibers surface.
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21

Gao, Feng. "Preparation, Polymerization, and Characterization of Sugar-based Microemulsion Glasses." University of Cincinnati / OhioLINK, 2007. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1186341421.

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22

Mathieson, William Bruce. "An electrosensory lateral line lobe slice preparation pyramidal cell electrophysiology." Thesis, University of Ottawa (Canada), 1987. http://hdl.handle.net/10393/5448.

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23

Tabe, Mohhamadi Abdulreza. "Preparation of highly selective polyamide membranes for gas separation applications." Thesis, University of Ottawa (Canada), 1995. http://hdl.handle.net/10393/9834.

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The use of reverse osmosis (RO) and ultrafiltration (UF) membranes for separation of gas mixtures is a relatively new development. Most of asymmetric RO and UF membranes which are useful in liquid separation fail to be effective in gas separation because some of the pores on the membrane surface are too large and have no separation capacity. The selectivity of these membranes can be improved by blocking the large pores with a second material. This process is known as coating and has proven to be highly effective in upgrading RO & UF membranes for gas separation. In this study membranes were prepared from an aromatic polyamide (PA) polymer and coated by silicone rubber. In a set of experiments, the permeation rates of six experimental gases through these membranes were measured at different pressures. The ideal separation factors higher than those reported in the literature were obtained. These results show that PA membranes are highly capable of separating the gases under investigation. The resistance model was employed to analyze the data and to explain the performance of this polymeric membrane. In another set of experiments, mixtures of CH$\sb4$/CO$\sb2$ with known compositions, and O$\sb2$/N$\sb2$ (air), were separated using coated PA membranes. The actual separation factors of 64 to 166 for CO$\sb2$/CH$\sb4$ and 8.7 for O$\sb2$/N$\sb2$ systems obtained in this set of experiments were higher than those reported in the literature. A "membrane-self-sealing" gas separation cell design allowed for a leak-free system with a leak rate of ${}1.2\times10\sp{-9}$ cm$\sp3$/s. This level of leak is few orders of magnitude lower than similar existing systems. This cell design facilitates experiments involving the separation of air in which a perfect sealing is necessary in order to prevent the oxygen enriched permeate to mix with the leaking air. The new separation cell was installed in a fully automated system which operates gas permeation experiments using a process control computer program. The system is designed such that measurement of permeation rates as low as $1\times10\sp{-8}$ cm$\sp3$/s becomes possible. The new system is ideal for experiments involving homogeneous membrane and/or low permeable gases such as nitrogen and methane.
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Gélinas, Stéphanie. "Preparation of magnetic carriers through functionalization of nanosized maghemite particles." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape8/PQDD_0023/NQ50168.pdf.

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25

Punwani, Karishma. "Automated control of the electron microscopy proteomic organellar preparation robot." Thesis, McGill University, 2005. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=99011.

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Electron microscopy (EM) is an important tool in organellar proteomics, where it is used to validate sample purity and to confirm protein presence. Current sample preparation techniques are manual, labor-intensive and time-consuming. To overcome these problems, an electron microscopy proteomic organellar preparation (EMPOP) robot is being developed for parallel preparation of up to 96 subcellular fraction samples in an efficient, repeatable and standardized manner. This thesis describes the development and validation of the software that controls the EMPOP robot. The software was organized in two coordinated levels consisting of a: (1) human-machine interface (HMI), and (2) low-level real-time control routines. The HMI was designed to be 'friendly and flexible', and to enable the operator to modify system parameters on-the-fly. Contrarily, the low-level control routines are responsible for controlling all EMPOP system processes. Pilot studies using the EMPOP system prove that the robot and software function predictably and consistently to generate high quality subcellular sample fractions.
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26

Santoso, Halim G. (Halim Gustiono) 1975. "Mixture preparation, combustion, and HC emissions at different cranking speeds." Thesis, Massachusetts Institute of Technology, 2002. http://hdl.handle.net/1721.1/89880.

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27

Ling, Yuanbing 1970. "Direct preparation of alpha-calcium sulfate hemihydrate from sulfuric acid." Thesis, McGill University, 2003. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=84283.

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In this work, the crystallization of alpha-calcium sulfate hemihydrate in sulfuric acid solution and the correlation between its properties and preparation conditions by reaction of sulfuric acid with lime (CaO) have been thoroughly investigated. The research involved the study of conversion-dissolution of calcium sulfate dihydrate in H2SO4 solution, the measurement of solubilities, thermo-dynamic calculations and the preparation of alpha-CaSO4 ·0.5 H2O via different methods of reactive mixing of H2SO4 and CaO. It was found that the calcium sulfate solids can saturate the sulfuric acid solutions in only 5 minutes. The solubility of calcium sulfate hemihydrate in 0--3.0M H 2SO4 solution at 100°C was experimentally determined and thermodynamic calculations with the aid of FactSage and OLI have led to establishment of the phase diagram for the CaSO4-H2SO 4-H2O system. An operating window has been determined in terms of H2SO4 concentration, temperature and time within which alpha-hemihydrate can be produced by reaction of lime with H 2SO4. This window is defined as 0.6--1.1M H2SO 4 (steady-state concentrations), 98--105°C and 1 hour retention time. Dihydrate was found to form as intermediate phase quickly converting to hemihydrate. The kinetics of conversion depends on the acidity level.
For the standard preparation procedure of adding lime into hot sulfuric acid, alpha-hemihydrate grows in the c-axis direction much more rapidly than in other directions ending in the form of fine needle crystals. Also, independent of the shape of the seed particles, the resultant crystals of hemihydrate are needle-shaped, which suggests a "dissolution-recrystallization" mechanism. Upon prolonged equilibration in their acid-preparation solution hemihydrate needle-shape crystals become fibrous and eventually convert to anhydrite. It is believed that uptake of SO42- instead of Ca2+ is the rate-determining step in the hemihydrate crystallization process. The hot SO42--rich environment rendered most of the additives (particularly organic) tried ineffective. Trivalent cations such as Fe3+ and Al3+, are the only ones found to modify the crystal morphology from needle-shape to small "grain" type morphology.
Slow addition of H2SO4 solution to slaked lime - reverse procedure was found to favor the production of alpha-hemihydrate with column-shaped as opposed to needle-shaped crystal morphology within otherwise the same operating window, 0.6--1.1M H2SO4. Preliminary assessment of the properties of the alpha-hemihydrate materials synthesized in this work showed them to compare satisfactorily with other materials produced by conversion of dihydrate to hemihydrate.
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28

Jameel, Ambreen. "Molybdenum-phosphate solution chemistry in the preparation of hydrosulphurisation catalysts." Thesis, Manchester Metropolitan University, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.300354.

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29

Borton, Peter Thomas. "Preparation and Characterization of Manganese Fulleride." University of Dayton / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=dayton1354556594.

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30

Keuler, Johan Nico. "Preparation and characterisation of palladium composite membranes." Thesis, Link to the online version, 1997. http://hdl.handle.net/10019/1431.

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Antti, Marta-Lena. "Preparation and properties of sapphire/alumina long fibre composites." Licentiate thesis, Luleå tekniska universitet, Institutionen för teknikvetenskap och matematik, 1999. http://urn.kb.se/resolve?urn=urn:nbn:se:ltu:diva-16924.

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The research described in the thesis concerns the preparation and properties of oxide/oxide composites and in particular composites consisting of an oxide matrix reinforced with continuous oxide fibres and intended for use as structural materials at very high temperatures. For this application particular attention must be paid to the behaviour of the fibre/matrix interface and to the properties of the fibre. The research has involved two main aspects (i) a thorough review of the physical and mechanical properties of candidate oxides with emphasis on elastic properties and creep properties and (ii) the experimental development of methods to produce continuous fibre reinforced oxide/oxide composites.

Godkänd; 1999; 20070404 (ysko)

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32

Page, Scott Lawrence. "Sound-induced micromechanical motions in an isolated cochlea preparation." Thesis, Massachusetts Institute of Technology, 2006. http://hdl.handle.net/1721.1/37926.

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Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, 2006.
Includes bibliographical references (p. 44-45).
The mechanical processes at work within the organ of Corti can be greatly elucidated by measuring both radial motions and traveling-wave behavior of structures within this organ in response to sound stimuli. To enable such measurements, we have developed a new preparation for observing three-dimensional motions of micromechanical structures in the apical region of an isolated gerbil cochlea. The cochlea is submerged in a low-chloride, low-calcium artificial perilymph solution and cemented to the bottom of a Petri dish at an angle. The bone above scala vestibuli of one half of the apical turn is removed to allow optical imaging with a 40x, 0.8 NA water-immersion objective. Reissner's membrane is left intact. Illumination is provided with a blue LED coupled to an optical fiber. The fiber is positioned next to the bone surrounding scala tympani of the apical turn, so that the organ of Corti is illuminated from below. The resulting optical access allows imaging of a variety of structures that have been proposed to play a role in cochlear mechanics, including inner and outer hair cell bundles, the tectorial membrane, inner and outer pillar cells, and efferent fibers in the tunnel of Corti. In some preparations, individual stereocilia of inner hair cell bundles can be resolved.
(cont.) Motions are stimulated by driving the stapes with a piezoelectric probe, and are measured using a stroboscopic computer microvision system. Measurements of sub-micrometer motions of key structures in three dimensions are quantified, including longitudinal motion of the organ of Corti and relative radial motion between the tectorial membrane and hair cells. Longitudinal motion of the Efferent fibers in the tunnel of Corti is found to have a phase lead with respect to the hair cell bodies. This system enables quantitative studies of both the relative motions of structures within the organ of Corti in response to sound and the propagation of traveling waves along structures within the organ of Corti.
by Scott Lawrence Page.
S.M.
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33

Marques-Garcia, Lourdes. "Preparation and characterisation of nanostructured bulk Bi2Te3 thermoelectric materials using ultrasound milling." Thesis, Cardiff University, 2016. http://orca.cf.ac.uk/93575/.

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Thermoelectric materials have been intensively investigated during the last years for energy harvesting applications. The main drawback of this technology is the low efficiency of the current materials. Significant advances in this respect have been recently achieved by nanostructuring, to mainly reduce the thermal conductivity. In this approach a bulk sample is milled into a nanostructured powder that is then compacted to form a nanobulk sample. The main objective of this thesis is to explore and introduce a new technique, ultrasound milling, based on the crushing of bulk samples by means of ultrasound effects taking place in a liquid medium, for the preparation of nanostructured bulk materials. Bismuth telluride alloys are the industrial standard in thermoelectrics and has been chosen as the material to perform this investigation. The most suitable conditions for the preparation of the nanostructured powders by the ultrasound milling technique have been identified. The optimised powders were used to prepare compacted nanobulk samples. The thermoelectric properties of these samples were finally characterised at room temperature and their performance related to their microstructure. Extraordinarily low thermal conductivity was obtained for both n- and p-type samples prepared (0.5 and 0.35 W/Km respectively), which are within the lowest reported values for any thermoelectric alloy. This reduction was accompanied with a significant decrease in electrical conductivity which led to a non-significant improvement in the figure of merit (Z). However, high ZT values (1 and 1.4 for n- and p-type bismuth telluride respectively) were identified in non-treated samples after a very simple grinding process which was employed as pre-treatment. The figure of merit of these two materials prepared by this simple methodology is close to the best reported values for Bi2Te3. Our results identify ultrasound milling and the simple crushing method as promising tools for the fabrication of nanostructured bulk thermoelectric materials.
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34

Tian, Bo. "Modified electroless plating technique for preparation of palladium composite membranes." Thesis, Link to the online version, 2005. http://hdl.handle.net/10019/1243.

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35

Tang, Qingmeng. "Preparation and Characterization of Electrically Conductive Graphene-Based Polymer Nanocomposites." Case Western Reserve University School of Graduate Studies / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=case1386260373.

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36

Kvarnlöf, Niklas. "Activation of dissolving pulps prior to viscose preparation." Doctoral thesis, Karlstad University, Faculty of Technology and Science, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:kau:diva-1276.

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The conventional viscose manufacturing process is a mature process that needs to be improved with respect to its environmental impact and its production cost structure. Therefore a research study has been done with the aim to improve the reactivity of the dissolving pulp used, in order to reduce the chemical demand in the viscose process and thus reduce the cost and indirectly the environmental impact.

The work described in this thesis has shown that it is possible to enhance the pulp reactivity and to use less carbon disulphide in the production of viscose, while maintaining a good quality viscose dope, by two entirely different pretreatment methods, one chemical and one enzymatic.

The chemical method used pressurized oxygen after the mercerisation step, which increased the reactivity of the alkali cellulose. The viscose dopes produced from the pressurized oxygen treated alkali cellulose had lower filter clogging values, Kw, compared to conventionally produced viscoses. The temperature and the oxygen treatment time of the alkali cellulose were however crucial for the viscose quality.

The best performing enzyme of several tested was a cellulase of the mono component endoglucanase preparation Carezyme®. This enzymatic treatment was optimized with respect to viscose dope preparation. The study showed that the enzyme treatment could be carried out under industrially interesting conditions with respect to temperature, enzyme dose and reaction time. A re-circulation study of the enzyme showed that it was possible to re-use the spent press water from the enzymatic treatment step several times, and thus lower the production cost. Some of the viscose process stages were modified to properly fit the enzymatically treated dissolving pulp and a comparison between viscose made from enzyme-treated pulp and viscose made from conventional pulp, showed that the enzyme-treated samples had a lower filter clogging value, Kw. This indirectly indicates that the enzyme pretreatment could reduce the carbon disulphide charge in the viscose manufacturing process. An initial study of how the Carezyme® influenced different cellulosic sources was also performed.

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37

Smith-Freshwater, Alicia P. "PREPARATION AND CHARACTERIZATION OF AN ELECTROSPUN GELATIN/DENDRIMER HYBRID NANOFIBER DRESSING." VCU Scholars Compass, 2009. http://scholarscompass.vcu.edu/etd/19.

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A novel dendritic wound dressing was designed and characterized for its potential to treat chronic wounds. Comprised of gelatin, dendrimer, synthetic polymer and antibiotics, the dressing was electrospun to mimic the natural extracellular matrix (ECM). Gelatin is biocompatible, biodegradable, non-toxic, and easily available. The antibiotic, doxycycline, has the ability to inhibit matrix metalloproteinases. Matrix metalloproteinases, which occur in excess in chronic wounds, degrade the reconstituted ECM. Starburst™ polyamidoamine (PAMAM) dendrimer G3.5, which provides a versatile and structurally controlled architecture to construct nanomedicine, was covalently bonded to the gelatin backbone and electrospun into nanofibers with gelatin, doxycycline and stabilizing polymers. The proposed gelatin/dendrimer hybrid provides a bacterial free environment and mimics the ECM to promote wound healing. The development of this new polymeric matrix is an important step in advancing the use of bioactive nanofibers with targeted and controlled drug delivery as a wound dressing.
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38

Almlöf, Heléne. "Extended Mercerization Prior to Carboxymethyl Cellulose Preparation." Licentiate thesis, Karlstads universitet, Avdelningen för kemiteknik, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:kau:diva-5947.

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Carboxymethyl cellulose (CMC) is produced commercially in a two-stage process consisting of a mercerization stage, where the pulp is treated with alkali in a water alcohol solution, followed by an etherification stage in which monochloroacetic acid is added to the pulp slurry. In this thesis an extended mercerization stage of a spruce ether pulp was investigated where the parameters studied were the ratio of cellulose I and II, concentration of alkali, temperature and retention time. The influence of the mercerization stage conditions on the etherification stage, were evaluated as the degree of substitution (DS) of the resulting CMC and the filterability of CMC dissolved in water at a concentration of 1%. The DS results suggested that the NaOH concentration in the mercerization stage was the most important of the parameters studied. When the NaOH concentration in the mercerization step was low (9%), a high cellulose II content in the pulp used was found to have no negative impact on the DS of the resulting CMC compared with pulps with only cellulose I. However, when the NaOH concentration was high (27.5%), pulps with high content of cellulose II showed a lower reactivity than those with only cellulose I with respect to the DS of the CMC obtained after a given charge of NaMCA. The results obtained from the filtration ability study of CMC water solutions suggested that both the amount of cellulose II in the original pulp and the temperature had a negative influence on the filtration ability whereas the NaOH concentration in the mercerization stage had a positive influence. The filtration ability was assumed to be influenced highly by the presence of poorly reacted cellulose segments. A retention time between 1-48 h in the mercerization stage had no effect on either the DS or the filtration ability of the CMC. Using NIR FT Raman spectroscopy molecular structures of CMC and its gel fraction were analyzed with respect to the conditions used in the extended mercerization stage. Here it was found that the alkaline concentration had a very strong influence on the following etherification reaction. FT Raman spectra of CMC samples and their gel fractions prepared with low NaOH concentrations (9%) in the mercerization stage indicated an incomplete transformation of cellulose to Na-cellulose before carboxymethylation to CMC. Low average DS values of the CMC, i.e. between 0.42 and 0.50, were yielded. Such CMC dissolved in water caused very thick and semi solid gum-like gels, probably due to an uneven distribution of substituting groups along the cellulose backbone. FT Raman spectra of CMC mercerized with alkaline concentrations at 18.25 and 27.5% in the mercerization stage indicated, however, that all of the cellulose molecules were totally transferred to CMC of high DS, i.e. between 0.88 and 1.05. When dissolved in water such CMC caused gels when they were prepared from ether pulp with a high fraction of cellulose II.
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39

Qurashi, Muhammad Tariq. "Preparation and characterisation of membranes of chitosan and modified chitosan." Thesis, Queen's University Belfast, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.335584.

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40

Dowell, Rachel J. (Rachel Jean). "Registration of 2D ultrasound images in preparation for 3D reconstruction." Thesis, Massachusetts Institute of Technology, 1997. http://hdl.handle.net/1721.1/10181.

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41

Han, Yang. "Preparation and characterization of a self-crimp side-by-side bicomponent electrospun material." VCU Scholars Compass, 2012. http://scholarscompass.vcu.edu/etd/2857.

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Bicomponent composite fibers have been widely used in the textile industry and are gaining increasing attention on biomedical applications. In this research, polycaprolactone/poly (lactic acid) side-by-side bicomponent fibers were created for the application of a biodegradable scaffold. The side-by-side structure endowed the fiber with self-crimps when it was processed under certain conditions. This material was produced by electrospinning and collected on a high speed rotating mandrel to get highly oriented fibers. A mechanical stretch at the same direction was done followed by a wet heat treatment for polymer retraction. Crimped fibers were demonstrated by scanning electron microscopy. The quantitative porosity and uniaxial tensile strength was not affected by the post-treatments, but the cell ingrowth and proliferation after seeding the scaffold were significantly improved. In conclusion, the side-by-side crimped material serves as a better extracellular matrix analogue without sacrificing mechanical properties.
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42

Afkhami, Zarreh Fatemeh. "Delivery of IFNa and VEGF165b by microencapsulated cells: preparation and «in vitro» analysis." Thesis, McGill University, 2009. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=66849.

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ABSTRACT The pivotal role of angiogenesis in the growth and spread of all solid tumors has driven the cancer research on applying antiangiogenic factors to suppress formation of new blood vessels in order to prevent or slow tumor growth. Glycoproteins, Interferon alpha (IFNα and VEGF165b are of particular interest in this study. IFNα is a multifunctional cytokine with many physiological effects including antiangiogenesis effects. VEGF165b is a competitive antagonist of the Vascular Endothelial Growth Factor (VEGF) receptor and has been reported to successfully inhibit angiogenesis. The thesis goal is to develop a system for simultaneous production of IFNα2b (IFNα) and VEGF165b and targeted delivery to enhance their antiangiogenic properties. For this purpose, HEK293 cells were developed to produce IFNα and VEGF165b simultaneously. The potential of a stable HEK293 cell line producing IFNα or VEGF165b to continuously deliver IFNα or VEGF165b after encapsulation in alginate-poly-l-lysine-alginate (APA) microcapsules was evaluated. For a better delivery system, co-encapsulation of HEK293 VEGF165b producing cells and HEK293 IFNα producing cells or a mixture of encapsulated HEK293 cells producing either IFNα or VEGF165b were studied. Attempts were also made to increase the bioactivity (pharmacodynamic) of IFNα by modifying its O-glycosylation to an N-glycosylation site and of VEGF165b by increasing its sialylation level. The bioactivity was investigated in experimental rats. The results suggest that one cell line, HEK293, can produce IFNα and VEGF165b simultaneously. This process has the advantage of ease of manipulation and low cost but is somewhat limited by the fact that production of IFNα and VEGF165b cannot be controlled. Microencapsulation of IFNα or VEGF165b producing cells demonstrates that encapsulated cells grow and remain viable within the microcapsules. The IFNα and VEGF165b released
RÉSUMÉLe IFNα est une cytokine multifonctionnelle avec plusieurs effets physiologiques incluant l'antiangiogenèse effets tandis que le VEGF165b est un antagoniste concurrentiel du récepteur de Vascular Endothelial Growth Factor (VEGF) et empêche avec succès l'angiogenèse. La thèse a pour but de développer un système pour la production simultanée du IFNα et du VEGF165b, de plus, que la livraison soit ciblée pour augmenter les propriétés antiangiogéniques. À cette fin, les cellules HEK293 ont été génétiquement modifiées pour produire simultanément l'IFNα et le VEGF165b. Le potentiel d'une lignée cellulaire HEK293 stable, produisant simultanément le IFNα ou VEGF165b pour livrer en perpétuité le IFNα et VEGF165b après l'encapsulation dans des microcapsules composé de l'alginate-poly-l-lysine-alginate (APA) a été évalué. Pour apporté des améliorations au système, deux mélanges ont été évalué. La co-encapsulation de cellules HEK293 produisant le VEGF165b et de cellules de HEK293 produisant IFNα et un mélange deux types de cellules encapsulées séparément ont été étudiés. Des tentatives ont été également accomplies pour augmenter leur bioactivité (pharmacodynamic) du IFNα en modifiant son O-glycosylation à un emplacement de N-glycosylation et de VEGF165b en augmentant son niveau de sialylation. La bioactivité a été étudiée chez les rats expérimentaux. Les résultats suggèrent que les cellules, HEK293, puissent produire l'IFNα et le VEGF165b simultanément. Ce processus a l'avantage de facilité la manipulation et de maintenir les coûts bas mais est légèrement limité par le fait que la production du d'IFNα et du VEG165Fb ne peut pas être contrôlée. Le microencapsulation de cellules produisant le IFNα ou VEGF165b démontrent que les cellules encapsulées se développent tout en retenant leur capacités de synthèses et demeurent viables d
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43

Kitsopanidis, Ioannis 1975. "Fuel targeting and thermal environment effects onf spark-ignition engine mixture preparation process." Thesis, Massachusetts Institute of Technology, 2000. http://hdl.handle.net/1721.1/88849.

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44

Pyle, Benjamin Ryan. "An analysis of the size-control and uniformity of polymeric nanoparticle preparation techniques." Thesis, Massachusetts Institute of Technology, 2013. http://hdl.handle.net/1721.1/83740.

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Thesis (S.B.)--Massachusetts Institute of Technology, Department of Mechanical Engineering, 2013.
Cataloged from PDF version of thesis.
Includes bibliographical references (pages 62-64).
Nanoparticles are bridge the gap between the micro and atomic scale and have found a variety of different used, especially in the drug-delivery field. This paper will break down some of the mot common methods for polymeric nanoparticle production.
by Benjamin Ryan Pyle.
S.B.
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45

Cowart, Jim S. (Jim Scot) 1966. "Mixture preparation behavior in port fuel injected spark ignition engines during transient operation." Thesis, Massachusetts Institute of Technology, 2000. http://hdl.handle.net/1721.1/89292.

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46

Chirinos, Maruri Ada Elida. "Influence of preparation techniques on the Fischer-Tropsch performance of supported cobalt catalysts." Doctoral thesis, University of Cape Town, 2003. http://hdl.handle.net/11427/5365.

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Includes bibliographical references.
Cobalt based catalysts are generally used for the FT synthesis due to their high activity and selectivity for linear hydrocarbons, low activity for the water gas shift reaction and lower price compared to noble metals [22]. There can, however, be a large effective loss of active metal due to strong metal-support interaction forming complexes that are not reduced at temperatures below 400°C.
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47

September, Caelin Gee. "Preparation and characterisation of inorganic nanostructured support materials for polymer electrolyte fuel cells." Master's thesis, University of Cape Town, 2015. http://hdl.handle.net/11427/20125.

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Polymer electrolyte fuel cells (PEFCs) have been identified as a safe, clean and reliable alternative energy conversion technology to conventional, fossil fuel based, ones. However, the hindrance to worldwide commercialisation of this technology lies in the poor durability and high costs associated with the current carbon supported platinum (Pt/C) catalysts. Carbon support corrosion and Pt dissolution/aggregation on the catalyst layer within the fuel cell have been confirmed as the major contributors to the degradation of the Pt/C (Shao, et al., 2007). Attention needs to be paid to the improvement of catalyst components to produce an electrocatalyst with better degradation resistance and low Pt loading in order to overcome these two major commercialisation barriers. The physico-chemical and electronic interaction between the Pt catalyst and the support material play a crucial role in the catalytic activity and stability of the electrocatalysts (Wang, et al., 2011). A comprehensive understanding of the effects of catalyst support material and morphology on the mechanism and kinetics of the oxygen reduction reaction (ORR) needs to be developed. This study investigated alternative, novel catalyst support materials and structures for the catalyst layer as opposed to carbon for PEFC applications. This material consisted of TiB2 electrospun nanofibers, powder and crushed electrospun nanofibers. Methods used to reliably and accurately deposit Pt onto these materials were identified, developed and analysed. These methods include platinum deposited onto TiB2 powder, electrospun crushed nanofibers and nanofiber mats via DC magnetron sputter deposition and thermally induced chemical deposition (TICD). The synthesised catalysts were physically characterised using X-ray diffraction (XRD), Transmission Electron Microscopy (TEM), Scanning Electron Microscopy (SEM) and Inductively Coupled Plasma Optical emission spectrometry (ICP-OES). Platinum effectively deposited on the TiB2 support structures via these deposition techniques within two standard deviations of the desired Pt loadings.
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48

Zamani, Davoud. "Lowering the Environmental Impact Of High-κ/Metal Gate Stack Surface Preparation Processes." Diss., The University of Arizona, 2012. http://hdl.handle.net/10150/265397.

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Hafnium based oxides and silicates are promising high-κ dielectrics to replace SiO₂ as gate material for state-of-the-art semiconductor devices. However, integrating these new high-κ materials into the existing complementary metal-oxide semiconductor (CMOS) process remains a challenge. One particular area of concern is the use of large amounts of HF during wet etching of hafnium based oxides and silicates. The patterning of thin films of these materials is accomplished by wet etching in HF solutions. The use of HF allows dissolution of hafnium as an anionic fluoride complex. Etch selectivity with respect to SiO₂ is achieved by appropriately diluting the solutions and using slightly elevated temperatures. From an ESH point of view, it would be beneficial to develop methods which would lower the use of HF. The first objective of this study is to find new chemistries and developments of new wet etch methods to reduce fluoride consumption during wet etching of hafnium based high-κ materials. Another related issue with major environmental impact is the usage of large amounts of rinsing water for removal of HF in post-etch cleaning step. Both of these require a better understanding of the HF interaction with the high-κ surface during the etching, cleaning, and rinsing processes. During the rinse, the cleaning chemical is removed from the wafers. Ensuring optimal resource usage and cycle time during the rinse requires a sound understanding and quantitative description of the transport effects that dominate the removal rate of the cleaning chemicals from the surfaces. Multiple processes, such as desorption and re-adsorption, diffusion, migration and convection, all factor into the removal rate of the cleaning chemical during the rinse. Any of these processes can be the removal rate limiting process, the bottleneck of the rinse. In fact, the process limiting the removal rate generally changes as the rinse progresses, offering the opportunity to save resources. The second objective of this study is to develop new rinse methods to reduce water and energy usage during rinsing and cleaning of hafnium based high-κ materials in single wafer-cleaning tools. It is necessary to have a metrology method which can study the effect of all process parameters that affect the rinsing by knowing surface concentration of contaminants in patterned hafnium based oxides and silicate wafers. This has been achieved by the introduction of a metrology method at The University of Arizona which monitors the transport of contaminant concentrations inside micro- and nano- structures. This is the only metrology which will be able to provide surface concentration of contaminants inside hafnium based oxides and silicate micro-structures while the rinsing process is taking place. The goal of this research is to study the effect of various process parameters on rinsing of patterned hafnium based oxides and silicate wafers, and modify a metrology method for end point detection.
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49

Pate, Patricia Lynne. "The Preparation of and Upper Atmospheric Effects on Kevlar Films." W&M ScholarWorks, 1990. https://scholarworks.wm.edu/etd/1539625590.

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50

Wei, Jiacheng. "Graphene in epoxy system : dispersion, preparation and reinforcement effect." Thesis, Northumbria University, 2017. http://nrl.northumbria.ac.uk/36264/.

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Epoxy is one of the most adaptable and widely sold high performance material in the world because of its excellent mechanical properties, thermal stability, chemical and corrosion resistance, low shrinkage, low cost, and ease of processing, etc. Graphene shows good potential for the fabrication of high performance polymer nanocomposites because of its unique planar structure and its superlative mechanical properties, thermal conductivity and excellent electrical conductivity. The layered structure allows a large surface contact area with the matrix and thus leads to improvements in the properties. This work aims at exploiting the potential use of graphene as a filler to reinforce epoxy matrix and the preparation of homogeneously dispersed epoxy/graphene nanocomposites. To explore the maximum property enhancement of graphene in epoxy, dispersion is the key factor. However, in the preparation of epoxy/graphene nanocomposites, there still exist some challenges. One of the largest obstacles it that graphene tends to reagglomerate in liquid epoxy, which is due to the strong van der Waals force on the graphene surface. If not properly dispersed, the agglomerated graphene will act as a defect within the matrix and consequently lower the properties of the nanocomposites. Therefore, the dispersion of graphene and the processing techniques should be studied. In this work, epoxy/graphene nanocomposites had been made by different processing techniques. Different characterization methods had been applied to evaluate the reinforcement effect. By end of this work, graphene dispersion techniques and sample preparation methods have been optimized. Epoxy/graphene nanocomposites have been prepared with enhanced properties.
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