Thesis (M.S.)--Worcester Polytechnic Institute. / Keywords: cartilage, tendon, light scattering. Includes bibliographical references (p. 60-61).

The effect of shear on the evolution of floc properties was investigated to analyse the flocculation mechanisms. Little fundamental attention has been given to the shear influence that often creates compact aggregates, while the floc characteristics might differ in other aggregating conditions. It is thus crucial to understand how flocs evolve to steady state, if their properties are to be 'tailored' to suit subsequent solids-liquid separation processes. In this work, flocculation of monodisperse latex particles of various sizes (60, 380, and 810 nm diameter) via electrolyte addition was carried out in a couette-flow and also in shear fields generated by an axial-flow impeller (Fluid foil A310) and a radial-flow impeller (Rushton R100) in standard mixing tanks. A small-angle light scattering technique was used to acquire information regarding the time variation of floc properties in a non-intrusive manner. The structure was quantified by a measure of fractal dimension, signifying the degree of floc compactness. Estimates of the average floc mass were also obtained from the aggregate scattering patterns. By monitoring the changes in floc structure and mass, corresponding to the size evolution; mechanisms of floc formation, fragmentation, and restructuring were identified. Aggregates of 60 and 380 nm particles were observed to grew larger initially, before decreasing to their equilibrium sizes at moderate shear rates (32 - 100 s-1) in a homogeneous shear environment. Floc restructuring at large length scales occurred extensively, and was responsible for the drop in size, particularly at the early stage of the process. Aggregates of 810 nm particles did not, however, display this behaviour. Flocs of larger primary particles were presumably susceptible to breakage rather than deformation, as they were weaker under comparable conditions. Denser aggregates were found when restructuring transpired, while comparatively tenuous flocs were observed when formation and breakage kinetics were the governing mechanisms. The disparity in floc behaviour at higher shear rates (246 s-1 - 330 s-1) was less apparent. The intense hydrodynamic stresses in those instances inevitably caused fragmentation, regardless of the intrinsic particle properties; hence the observed floc compaction was the product of break-up and re-aggregation. A population balance model, incorporating variation in floc structure, displayed comparable trends in size evolution; verifying that restructuring indeed took an important role under certain flocculation conditions. Similar phenomena were likewise observed with the flocculation in stirred tanks. The results reinforced findings in literature; that while circulation time controlled the process kinetics; the floc size was determined by the turbulent stresses. In addition, the maximum shear levels also influenced the floc structures, with denser aggregates produced in a shear field generated using the radial-flow impeller at equivalent energy dissipation per-unit mass. A correlation between non-dimensional floc factor that embodied the aggregate size and structure, and aggregation factor comprising the significant parameters from flocculation conditions, was proposed. The proposed relationship takes into account aspects such as the aggregate structure, interparticle forces, and particle concentration that are often overlooked in existing relationships, which usually only relate the maximum floc size to the applied energy dissipation rate. It thus provides an improved manner of presenting general flocculation data, as well as a means to predict floc properties produced under a specific aggregation condition. Future studies with increasingly complex systems that resemble real conditions are recommended in order to establish a practical understanding of the flocculation mechanisms, for the purpose of optimising the aggregate properties.

Tissue, in particular its mechanical properties, is of interest from a material science point of view. The collagen fiber framework found in nearly all tissue forms the basis for the tissue's behavior. Connective tissue provides more interesting behavior, designed to bear significant load in one direction, while retaining the ability to stretch in other directions. Contributing factors to such behavior are fiber diameter and orientation. Small angle scattering analysis has been developed over the past century. Particular attention has been paid to x-ray and neutron scattering, both of which characterize features on a nanometer scale. Small angle light scattering (SALS) has the ability to characterize features on a micron scale, and is thus suitable for the analysis of collage fibers. Scattering data from several tendons were analyzed using the Generalized Indirect Fourier Transform (GIFT) program developed by Dr. Otto Glatter. The data is fit using cubic B-splines, and transformed into a probability density distribution function (abbreviated PDDF or p(r)). The PDDF can then be interpreted to give an average fiber diameter, as well as other structural information. Since this type of analysis has never been performed on collagen fibers, emphasis was placed on validating small angle light scattering as an appropriate technique to characterize collagen fiber diameter. This was accomplished by comparing the results with optical microscopy. Results from SALS analysis agree with features observed by optical microscopy. Small angle light scattering analysis is able to provide an analysis of structures superior to that of optical microscopy. Small angle scatter theory provides a three dimensional analysis of the structure. On the other hand, optical microscopy provides only a two dimensional view of the sample. The structure of collagen fibers in tissue is certainly three dimensional, making small angle light scattering a more suitable technique for characterization.

No description available.

Master of Science / Department of Mechanical and Nuclear Engineering / Steven J. Eckels / Christopher M. Sorensen / Large specific surface areas and high concentrations of reactive edge and defect sites make NanoActive™ metal oxide powders ideal chemical adsorbents. These powders are dispersed in aerosol form to remediate toxic wastes and neutralize chemical and biological warfare agents. In the destructive adsorption of toxic chemicals, effective application requires particles be as small as possible, thus, maximizing surface area and number of edge and defect sites. Other applications, e.g. smoke clearing, require particles be large so they will settle in a timely manner. Ideally, particle size control could be engineered into powder dispersion devices. The purpose of this study was to explore particle cohesion and aerodynamic deaggregation mechanisms to enhance the design of powder dispersion devices. An aerosol generator and four experimental nozzles were designed to explore the most commonly referenced deaggregation mechanisms: particle acceleration, particles in shear and turbulent flows, and particle impaction. The powders were then dispersed through the nozzles with increasing flow rates. A small angle light scattering device was used to make in situ particle size measurements. The nozzle designed for impaction deaggregated the NanoActive™ MgO particles to a lesser degree than the other three nozzles, which deaggregated the particles to a similar degree. Flows in three of the four nozzles were simulated in a commercial computational fluid dynamics package. Theoretical particle and aggregate stresses from the literature were calculated using simulated data. These calculations suggest particle acceleration causes internal stresses roughly three orders of magnitude larger than shear and turbulent flows. These calculations, coupled with experimental data, lead to the conclusion that acceleration was the most significant cause of particle deaggregation in these experiments. Experimental data also identified the dependence of deaggregation on primary particle size and agglomerate structure. NanoActive™ powders with smaller primary particles exhibited higher resistance to deaggregation. Small primary particle size was thought to increase the magnitude of van der Waals interactions. These interactions were modeled and compared to theoretical deaggregation stresses previously mentioned. In conclusion, deaggregation is possible. However, the ideas of particle size control and a universal dispersion device seem elusive considering the material dependent nature of deaggregation.

Cellulosananofibriller (CNFs) hör till naturens mest fundamentala byggstenar och förser naturliga material, såsom den yttre cellväggen i trä, med en otrolig styrka och styvhet. Genom att imitera träets arkitektur öppnas möjligheter upp för tillverkning av nya, biobaserade och lättviktiga strukturella material med mekaniska egenskaper som överskrider de för glasfiber, metaller och legeringar. Den ingenjörsmässiga utmaningen ligger i att framgångsrikt lyckas överföra de önskade mekaniska egenskaperna hos CNFs till filament som kan användas i material för dagligt bruk. Vid flödesfokuserad spinning av extraherade CNFs påverkar många parametrar den slutgiltiga funktionaliteten och kvaliteten hos de resulterande filamenten. För att optimera dessa processparametrar är mätning av de spunna filamentens dimensioner ett viktigt moment. Av särskilt intresse är filamentbredden, eftersom den är avgörande för de mekaniska egenskaperna. Karakterisering av filamentbredden är i dagsläget en mycket tidskrävande process där varje filament mäts manuellt i optiskt mikroskop. Det huvudsakliga målet med detta projekt är att effektivisera den nuvarande mätprocessen med avseende på både hastighet och noggrannhet med hjälp av laserspridning. I denna rapport visar vi på minst en halvering av nuvarande mättid vid användandet av en 3D-printad laseruppställning istället för ett optiskt mikroskop vid mätning av filamentbredd. Våra resultat indikerar att mätsäkerheten generellt är högre för lasermetoden jämfört med mikroskopin. Genomsnittliga standardavvikelser för mätvärden på tunnaste bredden från mikroskopi samt de två olika kurvanpassningsmetoderna vid lasermätning rapporteras vara 1.62, 0.85 (Curve fit) respektive 1.59 (Minima matching). Standardavvikelserna för tunnaste bredd korrelerar dock inte direkt mot metodernas noggrannhet eftersom de spunna filamenten uppvisar en stor variation i bredd längs med längden. En närmare jämförelse mellan mätvärden för matchade punkter på ideala och defekta filament demonstrerar att icke-uniforma och defekta filament påverkar mätnoggrannheten för laserspridningen negativt. Sammantaget stödjer våra resultat det faktum att ett tunnare filament resulterar i bättre upplösning och mindre mätfel vid mätning med laserspridning. Våra resultat visar på den stora potentialen för laserspridning som en mer effektiv mätmetod vid karakterisering av cellulosafilamentbredd. / Cellulose nanofibrils (CNFs) are one of nature’s most fundamental building blocks, providing incredible strength and stiffness to natural materials, such as the outer cell wall layer in wood. By mimicking the architecture of wood, possibilities opens up for the fabrication of new, biobased, light-weight structural materials with mechanical properties exceeding that of glassfibers, metals and alloys. However, the engineering challenge lies in successfully managing to translate the desirable mechanical properties of the CNFs into filaments that can be used in everyday life materials. Throughout the process of spinning the extracted CNFs into filaments, many factors and parameters affect the ultimate functionality and performance of the resulting filaments. Measuring the dimensions of the spun filaments is a crucial step in further optimizing process parameters. The width of the filament especially, impacts its mechanical performance. The characterization of the cellulose filament width is currently very time-consuming as each filament is manually measured using optical microscopy. The primary goal of this project is to make the current characterization process more effective, with respect to both accuracy and speed of measurement, by using laser scattering. In this report, we demonstrate a reduction by more than a half in measurement time using a 3D-printed laser scattering setup instead of an optical microscope when measuring filament width. Our results indicate that the certainty in measurement is generally higher for lase rscattering compared to optical microscopy. The mean standard deviations (SD) for the smallest widths estimated with optical microscopy and the two curve fitting methods used for the laser measurements are reported to be 1.62, 0.85 (Curve fit) and 1.59 (Minima matching) respectively. However, standard deviations for the thinnest width does not correlate directly to the accuracy of the methods since the spun filaments show a large variation in width along the length. A closer comparison between measurement values for matched points at ideal and non-uniform filaments demonstrate that the accuracy of the laser measurements are dependent on the uniformity of the filaments, with non-uniform filaments negatively impacting the accuracy. Our overall results supports the fact that a thinner filament gives a better resolution and smaller error when measuring with laser. Our results provide evidence for the great potential of laser scattering as a more efficient method for cellulose filament width determination.