Quantum dots are a part of very important our technological future because of their intriguing and useful properties. These properties are different in character from those of the corresponding bulk material. Quantum dots are inorganic artificial semiconductor nanocrystal whose electrons influence their physical and chemical properties. Zinc oxide quantum dots were synthesized through an ethanol based precipitation via colloidal synthesis method at various pH values. Various emission colors were obtained because the excited quantum dots of various sizes emitted specific wavelengths of light. The emission spectra indicated that the pH dependent quantum dots were successfully synthesized. Zinc oxide quantum dots were also encapsulated and the luminescence properties examined. The quantum dots that were immobilized in polyisoprene (PI) through chemiluminescence (CL) analyses were found to be stable and were capable of continuing their luminescence properties with extended uses and long- term storage. Linear calibration curves were acquired for concentration of 8.75 x 10-5 M H2O2 in TCPO-CL.

Luminescence techniques are sensitive, selective, and widely used in analysis. Luminescence intensity is attenuated by quenchers. This research has focused on the use of surfactants such as CTAB, SDS, and TX-100 singly or together with TiO2 nanoparticles to evaluate their individual and combined effects on some fluorescent aromatic compounds such as pyrene, fluoranthene, anthracene, phenanthrene, and carbazole. Rutile phase TiO2 was synthesized using the low temperature sol-gel method. Carbazole and phenanthrene were severely quenched by all surfactants singly or in combination with TiO2. Anthracene and fluoranthene showed some enhancement in their luminescence intensity. The most dramatic effect was observed on the fluorescence intensity of pyrene. Pyrene showed enhanced fluorescence after degassing the solution alone or with the addition of the surfactants alone or in combination with TiO2 after degassing. These results showed that surfactants and TiO2 nanoparticles either singly or in combination should be useful for analysis employing luminescence techniques.

Sol-Gel techniques depend on the hydrolysis and condensation reactions of organosilicon precursors in aqueous media and, thus, provide an inclusive environment with bioaffinity. On the other hand, carbon nanotubes (CNTs), which possess unique electric, thermal, mechanical, and chemical properties, including their high surface area:volume ratio, can be further surface-functionalized to address different material or sensing demands. In this work we describe a new composite material that combines the unique sol-gel network with conductive CNTs. Hydrolysis and subsequent condensation of tetramethyloxysilane (TMOS) in the presence of CNTs result in the formation of a dense, homogeneous material. Properties of this composite material on electrode surfaces are discussed and novel sensing applications are described.

Den additiva tillverkningsindustrin associeras ofta med en hållbar hushållning av resurser. Trots detta har denna industriavfall med stor potential till vidare användning. Detta kandidatexamensarbete undersöker möjligheten att använda Polyamid 12 (PA12) avfall från selektiv lasersintring (SLS) i formen av filament till en annan additiv tillverkningsmetod, friformsframställning. Avfall från olika delar av SLS-processen försågs av life science företaget Cytiva. Olika blandningar av avfallen extruderades till filament. Innan extrudering undersöktes innehåll samt de termiska egenskaperna hos avfallet med hjälp av differentiell skanningskalometri (DSC), termogravimetrisk analys och fourier transform infraröd spektroskopi. Filamenten analyserades med dragprovning, DSC och svepelektronmikroskopi. Rent obearbetat PA12 pulver och ett kommersiellt PA12 filament användes som referenser vid jämförelse. Blandningarna innehållande avfall från SLS-printerns automatiska rengöringsprocess var kontaminerade med glaspartiklar och blev därför spröda och erhöll en skrovlig yta. Dessa filament gick inte att 3D-printa eftersom glaspartiklar ansamlades i munstycket av printern. Flera filament fick en ojäm och liten diameter och kunde därför inte användas i 3D-printern. Ojämn och liten diameter blev resultatet av bekymmer med sensorn som mäter diametern av filamenten. Dessa filament gjordes av granulerade utskrivna prototyper, pulver nära utskrivna delar och silat pulver långt ifrån de utskrivna delarna. Filament gjorda på blandningar innehållande avfall från dammsugaren som används för att rengöra SLS-printern kunde med framgång skrivas ut i 3D-printern. Dessa filament hade en jämn diameter och innehöll inga större kontamineringar. Det är därför genomförbart att tillverka filament av avfall från alla delar av SLS-processen även om inte alla filament kunde 3D-printas. / Additive manufacturing is often associated with sustainable use of resources. However, this industry still has material waste with great potential for further use. This bachelor thesis examines the opportunity of using Polyamide 12 (PA12) waste from Selective laser sintering (SLS) in the form of filaments for another additive manufacturing method, fused filament fabrication. Waste from different parts of the SLS process were provided from the life science company Cytiva. Several blends of the waste were made into filaments. Prior extrusion, the thermal properties and content of the waste were examined with differential scanning calorimetry (DSC), thermogravimetric analysis and fourier transform infrared spectroscopy. The filaments were analyzed by tensile testing, DSC and scanning electron microscopy. Pure virgin powder of PA12 and a commercial PA12 filament were used as a reference for comparison. The blends containing waste from the SLS printer’s automatic blasting was contaminated with glass beads which resulted in brittle filaments with a rough surface. These filaments were not possible to 3D print with due to accumulation of glass beads in the nozzle of the printer. Several filaments got an uneven and small diameter and could therefore not be 3D printed with. The small and uneven diameter was a result of issues with the sensor measuring the diameter. This includes filaments made of granulated printed prototypes, powder close to the printed parts and sieved powder further away from printed parts. The filaments made of blends including waste from the vacuum cleaner used to clean the SLS printer could successfully be used in printing. These filaments had an even diameter and did not contain any larger contaminations. It is therefore possible to make filaments from waste from all parts of the SLS process although not all filaments could be 3D printed.

Microfluidic paper based analytical devices (microPADs) are a novel platform for point of care (POC) diagnostics. Limitations of reagent shelf life have been overcome with the introduction of reagent pencils as a method for solid-based reagent deposition. While useful, little work has been reported on the characterization and optimization of reagent pencils. Herein, an investigation on reagent pencil composition and efficiency is conducted via colorimetric release profile tests utilizing an erioglaucine disodium salt that yields a quantifiable blue colored product in the presence of water. Within this work, an investigation on the molecular weight dependence, polymer chain end functionality, and polymer-graphite ratio was conducted to determine the most desirable parameters in reagent pencil composition. Further, the effects of enzyme stability in the presence of poly(ethylene glycol) (PEG) is investigated. To show the versatility of reagent pencils, a novel reagent pencil incorporating a stimuli responsive polymer, poly(N-isporopylacrylamide) (PNIPAM) was developed. In this work, PNIPAM’s lower critical solution temperature (LCST) was manipulated with various salt solutions to control fluid flow both laterally and vertically through various microPAD designs. It was found that, while PNIPAM successfully blocked or retarded fluid flow in microPADs, the effect was limited when DI H2O wash solutions were run prior to salt solutions. To counteract this, PNIPAM was successfully covalently bound to alkene modified chromatography paper via thiolene click chemistry to reinforce solution wash tolerance.

When slow wear mechanisms are studied it is important to examine slower processes, such as diffusion. Such processes can have a significant impact over time and can cause other phases to form, which can have a large effect on the wear. This thesis has investigated the diffusion that is believed to take place between brass and cemented carbide tools. This was done to further the understanding of the slow atomic wear which if properly understood, could lead to solutions that would increase the lifetime of the tools. The diffusion pairs were made from a tribological contact and then heat treated to speed up the diffusion process. Different temperatures and times were tested, from 400 °C for 3 h to 700 °C for 24 h. The samples were analysed with SEM and EDS both before and after the heat treatment, to see if diffusion had taken place. However, because of many unexpected processes and reactions the analysis could not confirm that diffusion had taken place. The transportation of Cu at the higher temperatures was much faster than expected, and in some samples, Cu could not be detected after the heating. Since the surface was so mobile, the slower diffusion process did not have time to take place. Many improvements for future experiments are suggested to be able to observe the diffusion, such as depositing a thin film or adding more work material.

The market is in great need of more environmentally friendly alternatives to fossil-based composite materials to obtain a more sustainable future. Lignin is the second most common biopolymer and is a byproduct in the pulping and paper industry. Fractionation of lignin has made it possible to receive lignin with narrow dispersity and low molecular weight, which is suitable for further applications. Modification of lignin structure yields new reactive sites that can be tailored for specific needs. Because of the aromatic structure of lignin, it is a promising renewable resource for production of thermosets. In this project Kraft lignin is sequentially solvent-fractionated and modified in an allylation process with allyl chloride. The allylated lignin is reacted with a cross-linking agent and used to impregnate carbon fibre mats. The resin-coated material is then cured at 125 oC to achieve a composite material. The project also encompasses characterization of the chemical structure of lignin in the different fractions. The morphology and adhesive properties of the lignin as well as the carbon fibres and the composite material was investigated. Although the production of composite material from lignin and carbon fibres were accomplished, bubble formation in the resin was a problem for all composite samples that were prepared, whether it was during solvent evaporation or during curing. By performing the addition of resin to carbon fibre mats in multiple steps, where pressure is added after the first applied layer, it is suggested that complete adhesion to the carbon fibre can be achieved, whilst maintaining adequate resin to carbon fibre ratio. / Marknaden är i stort behov av mer miljövänliga alternativ till fossilbaserade kompositmaterial för att kunna erhålla en mer hållbar framtid. Lignin är den näst vanligaste aromatiska biopolymeren och framställs som en biprodukt i pappersindustrin. Fraktionering av lignin har gjort det möjligt att erhålla lignin med låg dispersitet och molekylvikt vilket är lämpligt för vidare applikationer. Modifiering av lignins struktur ger upphov till nya reaktiva grupper som kan anpassas för ens behov. Den aromatiska strukturen som lignin besitter resulterar i en lovande förnybar resurs för produktion av härdplast. I detta projekt är Kraft lignin sekventiellt fraktionerat med lösningsmedel och modifierat med hjälp av en allyleringsprocess i närvaro av allylklorid. Det allylerade ligninet reagerar med en tvärbindare och används vidare för att impregnera kolfiber. De impregnerade kolfibermattorna härdades i ugn vid 125 oC för att erhålla kompositmaterial. Projektet omfattar även karaktärisering av den kemiska strukturen i lignin från de olika fraktionerna. Morfologin och vidhäftningsförmåga av lignin, kolfiber och likaså kompositmaterialet undersöktes. Ett kompositmaterial bestående av kolfiber och lignin erhölls med framgång under projektets gång, dock var bubbelbildning ett stort problem under förångningen av lösningsmedel och även under härdningsprocessen. Addition av harts till kolfibermattorna i flera steg, där tryck är adderat efter det första lagret har blivit applicerat, anses vara en lovande metod för att en hög vidhäftningsgrad ska kunna erhållas. Detta medan ett adekvat förhållande mellan harts och kolfiber upprätthålls.

Multifunctional drug delivery systems incorporated with stimuli-sensitive drug release, magnetic nanoparticles and magnetic resonance (MR) T2 contrast agents is attracting increasing attention recently. In this thesis, works on polymer nanospheres response to temperature change, superparamagnetic iron oxide nanoparticles (SPION)/polymeric composite materials for MR imaging contrast agents are summarized. A “shell-in-shell” polymeric structure has been constructed through a “modified double-emulsion method”. Thermosensitive inner shell is comprised of poly(N-isopropylacrylamide) which undergoes phase transition at body temperature. Such a feature could facilitate drug release at an elevated temperature upon administration. Furthermore, the dual-shell structure is covered by a layer of gold nanoparticles. According to the cytotoxicity tests, the biocompatibility is shown to be enhanced due to the layer of gold. SPION have been prepared using a high temperature decomposition method. Particle growth of SPION is monitored by transmission electron microscope and synchrotron X-ray diffraction. Poly(L,L-lactide)@SPION (PLLA@SPION) composite particles have been prepared through surface-initiated ring-opening polymerization which has been developed in our lab. For biomedical applications, it is essential to transfer the particles to physiological solutions from organic solutions. Phase transfer of SPION has been carried out by utilizing small molecules. Stability at the neutral pH is of large concern for such transfer systems. A novel phase transfer agent, Pluronic F127 (PF127), a triblock copolymer has been applied and the stability of the aqueous PF127@oleic acid (OA)@SPION solution has been greatly enhanced over a broad pH range. Most interestingly, PF127@OA@SPION show remarkable efficacy as T2 contrast agents as indicated by relaxometric measurements compared with commercially available products. / QC 20101115

Polymer matrices are commonly used as guest-host systems for organic chromophores for use in non-linear optical materials. The chromophores must be aligned or poled in an electric field in order to impart anisotropy and non-linear activity to the material. This poling process raises several issues, the two largest being the eventual relaxation of the chromophores back into random orientations due to brownian motion, and high molecular weight polymer matrices limiting chromophore mobility during poling. The prevention of this relaxation process is an area of significant interest, especially in applications that require long term coating stability and activity. In this study, a polymer matrix is synthesized that seeks to solve both of these problems with one system. The ideal system would be one that allows for chromophore mobility during processing, but once chromophores have reached the desired orientation, limits mobility and relaxation during in-service usage. A copolymer of methyl methacrylate and a Diels-Alder adduct cross-linking monomer was synthesized in order to meet these challenges. This polymer was blended with commercially available acrylic polymer and organic chromophore molecules in order to test the viability of the solution. It was found that at the percent composition of cross-linker being utilized in the study, the Diels-Alder linkages were not reforming in any measurable amount due to the low amount of Diels-Alder active monomer units. This led to the development of a new system based on mixing polyfuran based polymers with polymaleimide based polymers during processing. This method allows for high amounts of cross-linking after processing ceases, which achieves both initial goals of the project, as well as allowing facile synthesis of the desired polymer components. Another attempt to address these issues in polymer matrix formation led to the use of a novel inimer system. The cross-linking agent was also the polymerization initiator, and these functionalities were separated by a Diels-Alder linkage that would fall apart upon exposure to thermal stimulus. These polymers were synthesized and isolated easily, although in some cases gelation occurred. In order to observe the extent of the cross-linking inimer being incorporated into the matrix, cleavage experiments were performed to induce the breaking of the Diels-Alder adduct. Analyzing the Diels-Alder cleaved polymer led to an interesting result: all polymers showed an increase in apparent molecular weight when analyzed by gel permeation chromatography. The increase in molecular weight occurring upon cleavage of main chain bonds has never before been observed in literature. The explanation proposed was that the polymer adopted a "ropeball" like topology consisting of tightly coiled loops and knots. Upon cleavage of the cross-links, the ropeball was able to unwind into a much more linear topology, occupying a much larger hydrodynamic volume. This increase in hydrodynamic volume would cause the gel permeation chromatography results to show an apparent increase in molecular weight.

One less commonly used “click” reaction is thiazolidine chemistry. Thiazolidine chemistry is a commonly used reaction used in biological systems because the reaction requires the presence of both cysteine (a common amino acid) and an aldehyde or ketone. If cysteine residues could be incorporated into a polymer then a variety of applications could be developed. Polymers containing free thiols (aka thiomers) have developed in the last decade to become great mucoadhesives. If there was a facile route to control the amount of free thiols along the polymer then more fine-tuned and potentially stronger adhesives could be made. For these reasons the attachment of cysteine residues in a facile way via reversible addition fragmentation chain transfer (RAFT) polymerization or small molecule synthesis was researched. The incorporation of latent cysteine residues into the polymer via post polymerization modification proved to be less successful. However protected cysteine molecules have been successfully ligated onto polymerizable monomers and have been show to be easily deprotected in the presence of an acid source.