Spinneret based Tunable Engineered Parameters (STEP) Platform is a recently reported pseudo-dry spinning and non-electrospinning technique that allows for the deposition of aligned polymeric nano-fibers with control on fiber diameters and orientation in single and multiple layers (diameter: sub 100nm micron, length: mm-cm), deposition (parallelism 2.5 degrees) and spacing (microns)). A wide range of polymers such as PLGA, PLA, PS, and PU have been utilized for their unique material properties in scaffold design. In this thesis two unique bioscaffolds are demonstrated for the measurement of group cell migration for wound closure and single cell contractility force for the study of force modulation. The wound healing assay bridges the gap between confluent reservoirs of NIH3T3 fibroblasts through arrangement of a suspended array of fibers guiding group cell migration along the fiber axis. This platform demonstrates that topographical and geometrical features of suspended fibers play a very important role in wound closure. Spacing, alignment and orientation were optimized to shown an increased rate of closure. In the second complementary assay, we report a fused-fiber network of suspended fibers capable of measuring single cell forces. Results from our experiments demonstrate that force behavior is dependent on mechanical properties such as stiffness and geometry of fiber networks. We also demonstrate changes in spatial and temporal organization of focal adhesion zyxin in response to single cell migration on these networks. / Master of Science

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yes / Creation of functional skin substitutes within a clinically acceptable time window is essential for timely repair and management of large wounds such as extensive burns. The aim of this study was to investigate the possibility of fabricating skin substitutes via a bottom-up nanofiber-enabled cell assembly approach and using such substitutes for full-thickness wound repair in nude mice. Following a layer-by-layer (L-b-L) manner, human primary skin cells (fibroblasts and keratinocytes) were rapidly assembled together with electrospun polycaprolactone (PCL)/collagen (3:1 w/w, 8% w/v) nanofibers into 3D constructs, in which fibroblasts and keratinocytes were located in the bottom and upper portion respectively. Following culture, the constructs developed into a skin-like structure with expression of basal keratinocyte markers and deposition of new matrix while exhibited good mechanical strength (as high as 4.0 MPa by 14 days). Treatment of the full-thickness wounds created on the back of nude mice with various grafts (acellular nanofiber meshes, dermal substitutes, skin substitutes and autografts) revealed that 14-day-cultured skin substitutes facilitated a rapid wound closure with complete epithelialization comparable to autografts. Taken together, skin-like substitutes can be formed by L-b-L assembling human skin cells and biomimetic nanofibers and they are effective to heal acute full-thickness wounds in nude mice.

Yes / In this study, polyacrylonitrile (PAN_P) nanofibers (NFs) were fabricated by electrospinning. The PAN_P NFs membrane was functionalized with diethylenetriamine to prepare a functionalized polyacrylonitrile (PAN_F) NFs membrane. TiO2 nanoparticles (NPs) synthesized in the laboratory were anchored to the surface of the PAN_F NFs membrane by electrospray to prepare a TiO2 NPs coated NFs membrane (PAN_Coa). A second TiO2/PAN_P composite membrane (PAN_Co) was prepared by embedding TiO2 NPs into the PAN_P NFs by electrospinning. The membranes were characterized by microscopic, spectroscopic and X-ray techniques. Scanning electron micrographs (SEM) revealed smooth morphologies for PAN_P and PAN_F NFs membranes and a dense cloud of TiO2 NPs on the surface of PAN_Coa NFs membrane. The attenuated total reflectance in the infrared (ATR-IR) proved the addition of the new amine functionality to the chemical structure of PAN. Transmission electron microscope images (TEM) revealed spherical TiO2 NPs with sizes between 18 and 32 nm. X-ray powder diffraction (XRD) patterns and energy dispersive X-ray spectroscopy (EDX) confirmed the existence of the anatase phase of TiO2. Surface profilometry da-ta showed increased surface roughness for the PAN_F and PAN_Coa NFs membranes. The adsorption-desorption isotherms and hysteresis loops for all NFs membranes followed the IV -isotherm and the H3 -hysteresis loop, corresponding to mesoporous and slit pores, respectively. The photocatalytic activities of PAN_Coa and PAN_Co NFs membranes against methyl orange dye degradation were evaluated and compared with those of bare TiO2 NPs.The higher photocatalytic activity of PAN_Coa membrane (92%, 20 ppm) compared to (PAN_Co) NFs membrane (41.64%, 20 ppm) and bare TiO2 (49.60%, 20 ppm) was attributed to the synergy between adsorption, lower band gap, high surface roughness and surface area.

Yes / Owing to their small size, good wettability, uniform dispersion ability and high thermal properties, the nickel-plated carbon nanotubes (Ni-CNTs) with different aspect ratios are used to reinforce reactive powder concrete (RPC) through modifying the nano/micro- structural units of concrete. Incorporating only 0.075 vol% of Ni-CNTs (0.03 vol% of CNTs) can significantly increase mechanical properties of RPC. The enhancement effect on compressive strength caused by the incorporation of Ni-CNTs with aspect ratio of 1000 reaches 26.8%/23.0 MPa, mainly benefiting from the high polymerization C-S-H gels, low porosity, and refined pore structure. The 33.5%/1.92 MPa increases of flexural strength can be attributed to the decrease of large pore, original cracks, molar ratio of CaO to SiO2, and gel water content when Ni-CNTs with aspect ratio of 125 are added. Ni-CNTs with aspect ratio of 1500 have the largest utilization rate of being pulled-out, resulting from the improvement of dispersibility and the pining effect of nickel coating and then leading to the increased toughness. Therefore, incorporating Ni-CNTs can fundamentally modify the nano/micro- scale structural nature of RPC, providing a bottom-up approach for controlling the properties of RPC. / Funding supported from the National Science Foundation of China (51908103 and 51978127) and the China Postdoctoral Science Foundation (2019M651116).

This diploma thesis focuses on the fabrication of ceramic fibres by electrospinning. The theoretical part of the thesis summarizes the currently available information regarding ceramic fibres, their properties, applications and fabrication. The theoretical part also describes the process of electrospinning as one of the most frequently used methods of nanofibre fabrication, as well as the parametres influencing this process. The experimental part is aimed at the fabrication of ceramic fibres based on titania, pure non-doped zirconia and yttria-doped zirconia by electrospinning and at the characterization of thus fabricated fibres. Ceramic precursors based on propoxide and polyvinylpyrrolidone were subjected to electrospinning. The experimental part of this diploma thesis also describes the influence of precursor composition, process conditions and calcination temperature on the morphology and phase composition of the fibres. Precursors were characterized by viscosity measurements. Thermogravimetric analysis (TGA), Röntgen analysis (RTG) and scanning electron microscopy (SEM) were used to describe the fibres. By performing electrospinning of precursors based on titanium propoxide and subsequent calcination at 500-1300 °C, TiO2 fibres with thickness of 100-2500 nm were fabricated. The phase composition changed with calcination temperature from 500 °C from anatase phase through rutile blend to pure rutile at 900 °C. By performing electrospinning of precursors based on zirconium propoxide and subsequent calcination at 550-1100 °C, 0 – 8 mol% Y2O3 doped ZrO2 fibres with thickness of 50-1000 nm were fabricated. An analysis of fibres based on non-doped ZrO2, calcined at 550 °C showed a composition of predominantly monoclinic phase. An analysis of 3 or 8 mol% Y2O3 doped ZrO2 fibres calcined at 900 °C showed a composition of predominantly tetragonal phase or purely cubic phase, respectively. With the increasing calcination temperature, the morphology of the fibres changed from porous nanostructure to chain-like non-porous structure consisting of micrometer grains of TiO2 or ZrO2. The ZrO2 fibres calcined at 700 °C remained flexible as well as the spun ones, while their fragility increased with the increase in calcination temperature.

D. Tech. (Department of Chemistry, Faculty of Applied and Computer Sciences), Vaal University of Technology. / Nanoscience receives a lot of attention in the 21 century and is one of the most advancing technology in our days. It provides many new and advanced technological opportunities. This field involves many disciplines which include chemical, physical, and biological related fields. The advancement of nanoscience makes life to be better and bring about new inventions which can solve many problems in our day to day life. Although there are reservations about the use of these materials in other fields. Some researchers believe that these materials can be a problem to the environment and humanity at large. Therefore, more research needs to be done to fully understand these materials. Polymer science is another field that has been advancing every day. Many problems in our lives require material which have properties from nanomaterials and polymers. The combination of these technologies can leads to new materials which have many possibilities in solving most problems. Some researchers have taken advantage of these two powerful fields and merge them. There has been a lot of work done that involves combination of nanotechnology and polymer science. The current project is an initiative to manufacture nanofibers. These fibers are prepared using polymer solution mixed with metal oxide and metal selenide nanomaterials. The polymer solution is incorporated with nanoparticles and electrospunned to make nanofibers. The electrospinning afford the material prepared to be at nanoscale. The fact that the material formed is at nanoscale opens many possibilities to be used in various fields. The study is about fabrication of polymer nanofibers embedded with metal chalcogenide nanoparticles. The metal oxide and metal selenide nanoparticles were prepared using complexes. These complexes contain both the metal and the chalcogenide of interest. The complexes are prepared from oxygen-based (urea), and selenium-based (diphenyldiselenide) ligands. The urea complexes co-ordinates with metal using oxygen for iron, however in silver complexes both nitrogen and oxygen are used. These complexes allow easy control of reaction parameters, and thermal decomposes to form metal oxide, metal selenide, and metal. The complexes are very stable and decomposes at about 200 °C. These compounds are thermal decomposed to form metal chalcogenides, and metal nanoparticles. The complexes are characterized with FTIR, TGA, and elemental analysis. The metal chalcoginedes (copper oxide, iron oxide, silver oxide, copper selenide, iron selenide, and silver selenide) nanoparticles were prepared using thermal decomposition of a single source (complexes or metal salts). The prepared chalcogenides nanoparticles have good absorption and emission properties consistent with small sizes. These nanoparticles are composed of various phased and stoichiometry. Some metal chalcogenides have a mixture of stoichiometry and phase. The metal chalcogenides nanoparticles are dominated by spheres, and other shapes such as rods. These metal chalcogenides have a particles size in the range of 1-36 nm. The metal chalcogenides nanoparticles were tested against bacteria and fungi. These nanoparticles show highest activity in gram positive compared to gram negative bacteria. Metal oxide nanoparticles show the highest activity compared to metal selenide. All the metal chalcogenides show the highest against fungi. The nanoparticles are able to inhibit the fungi at lowest concentration. The nanoparticles are characterized with various instruments which includes UV-Vis, PL, XRD, and TEM. Nanofibers of poly(methyl methacrylate) (PMMA) incorporated with metal selenide and metal oxide nanoparticles were prepared by electrospinning. The nanofibers incorporated with metal chalcogenide are more thermal stable than PMMA nanofibers. Therefore, incorporation of metal chalcogenides nanoparticles leads to more thermal stability nanofibers. The PMMA are coordinated to the metal oxide and metal selenide through carbonyl oxygen atom. The PMMA incorporated with metal oxide and metal selenide leads to the formation of nanofibers with uneven surface with a diameter in the range of 30 to 200 nm. The prepared fibers are characterized using FTIR, TGA, SEM.

Master of Science / Department of Mechanical and Nuclear Engineering / Youqi Wang / Electrospinning is one of the most versatile methods used to fabricate nanofibers. Sub micron and nano level fibers can be continuously produced with the help of an external electric field induced on the polymer melt. These nanofibers can be used in a large variety of applications such as biosensors, three dimensional tissue scaffolds, composites, electronic devices, etc. A unique feature of electrospinning is its ability to work with different fiber assemblies. This helps in making application specific changes and also increases the quality and performance of the fibers. PEO (polyethylene oxide) and electrostrictive graft elastomer (an electroactive polymer developed by NASA) were used in our experiments which focus on controlling the shape and alignment of the fibers. Electroactive polymers (EAP’s) are seen as the basis for future artificial muscles because of their ability to deform when external voltage is applied and quickly recover to their original form when the polarity of the applied voltage is reversed. Hence, aligned fibers of the electrostrictive graft elastomer were produced to mimic the alignment in human muscle fibers. Alignment of fibers is the main objective of this research and was facilitated using vacuum technology. The research was basically divided into three phases, starting with checking of the repeatability of the previously developed techniques using polyethylene oxide. Next, the electrostrictive graft elastomer was spun using the electrospinning techniques and was checked for alignment using the Coaxial Electrode method and PLC controlled secondary electric field method. Finally, a vacuum chamber was designed and built with new components and the elastomer was tested for improved alignment in vacuum using the PLC controlled secondary electric field method.

Thesis (MScEng (Process Engineering))--University of Stellenbosch, 2009. / The study concerns the use of the electrospinning technique for the formation of cellulose acetate hollow nanofibers. These hollow fibers are used to manufacture hollow fiber membranes. Important properties that should be inherent to these hollow-nanofibers include excellent permeability and separation characteristics, and long useful life. They have potential applications in filtration, reverse osmosis, and the separation of liquids and gases. It is apparent from the available literature on electrospinning and co-electrospinning that the diameter and the morphology of the resulting fibers are significantly influenced by variations in the system and process parameters, which include the solution concentration, solvent volatility, solution viscosity, surface tension and the conductivity of the spinning solution. The materials used include cellulose acetate (CA) (concentration = 11~14 wt %), (feed rate = 1~3 ml/h), acetone:dioxane (2:1) and mineral oil (feed rate = 0.5~1 ml/h) with core and shell linear velocity of 2 and 0.7 mm/min respectively. These materials were used as received without further purification. The co-electrospinning setup used comprised a compound spinneret, consisting of two concentric small-diameter capillary tubes/needles, one located inside another (core-shell/co-axial design). The internal and external diameters of the inside and outside needles were 0.3 and 1.2 mm respectively (0.3 mm shell/core gap space). The liquids CA (shell) and mineral oil (core) are pumped to the coaxial needle by a syringe pump, forming a compound droplet at the tip of the needle. A high voltage source is used to apply a potential of several kilovolts over the electrospinning distance. One electrode is placed into the spinning solution and the other oppositely charged (or neutral) electrode attached to a conductive collector. If the charge build up reaches approximately 15 kV the charged compound droplet, (poorly conductive polymer solution) deforms into a conical structure called a Taylor cone. On further increasing, the charge at the Taylor cone to some critical value (unique to each polymer system) the surface tension of the compound Taylor cone is broken and a core-shell jet of polymer solution ejects from the apex of the Taylor cone. This jet is linear over a small distance, and then deviates in a course of violent whipping from bending instabilities brought about by repulsive charges existing along the jet length. The core-shell jet is stretched and solvent is evaporated and expelled, resulting in the thinning and alignment of the fiber. Ultimately dry (most solvent having been removed) submicron fibers are collected in alignment form in a simple collector design (water bath). The shell to core solution flow rate ratio was chosen according to the parameter response of shell-core diameter of the resulting fibers in order to achieve an optimal hollow structure after removal of the mineral oil core. The mineral oil of the dry collected core-shell fibers is removed by immersion in octane. The aforementioned response is determined by measurement of core-shell diameters using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The obtained results showed that the ability of the spinning solution to be electrospun was directly dependent on its concentration and the feed rate of the spinning solution and also parameters such as the spinning distance and type of solvents used. The preferable polymer solution concentration is 14 wt %, shell feed rate of 3 ml/hr, core feed rate of 0.5 ml/hr (2 and 0.7 mm/s core and shell linear velocity respectively), applied voltage of 15 KV, spinning distance of 8 cm and coaxial spinnerets having internal diameters of 0.3 mm and 1.2 mm core and shell needles respectively (0.3 mm shell/core gap space) have been found to make uniform cellulose acetate hollow fibers with an average inside and outside diameter of approximately 495 and 1266 nm, respectively.