Matching Items (25)
Description
I worked with Professor Long and the Long research group in the Biodesign Institute to develop an ultra-violet assisted direct ink write 3D printer to 3D print poly(amic acid) pendant salts for their group. The project included a proof of concept small format 3D printer and then the development of the full scale printer. I wrote custom code to run the printer and create complex models as well as code to automatic dispense the viscous polymer we were using.
ContributorsLogsdon, Andrew (Author) / Long, Timothy (Thesis director) / Jin, Kailong (Committee member) / Barrett, The Honors College (Contributor) / Mechanical and Aerospace Engineering Program (Contributor)
Created2021-12
Description
Biomimetics is a field where natural and biological systems are replicated in a lab. The evolved hierarchical designs of the floating leaves of the water fern Salvinia Molesta are taken as inspiration as they reveal excellent dual scale roughness capability which also presents superhydrophobic properties in the nature. The microscale eggbeater-shaped hairs are coated with microscopic granules and nanoscopic wax crystals (dual-scale roughness) and wrinkled hydrophilic patches are coated with wax crystals which are evenly distributed on the terminal of each hair. The combination of features with diverse wettability, such as wrinkled hydrophilic patches atop superhydrophobic eggbeater hairs, makes such structures unique. The hydrophilic patches bind the air-water interface to the tips of the eggbeater hairs and inhibit air bubble formation. Salvinia effect of several Salvinia species has been extensively researched. Superhydrophobicity is attracting increasing attention for various applications. Salvinia exhibit multiscale roughness because of the unique combination of smooth hydrophilic patches on elastic eggbeater structures decorated with nanoscopic wax crystals. However, how to reproduce such hierarchical structures with controllable surface roughness is challenging for current fabrication approaches, which hinders the applications of these superhydrophobic properties as well as multi-scale roughness on surfaces in engineered products.The objective of this research is to fabricate and study the superhydrophobic structures using electrically assisted Vat Photopolymerization. In this project, an electrically assisted Vat Photopolymerization 3D printing (e-VPP-3DP) process was developed to control the surface roughness of printed eggbeater structures with distribution of multi walled carbon nanotubes (MWCNTs) for multi scale roughness. Vat Photopolymerization (VPP) is a Photopolymerization technique where a Photo Curable resin is used to rapidly produce dense photopolymer parts. A fundamental understanding of e-VPP technique to create superhydrophobic structures was studied to identify the relation between geometric morphology and mechanical enhancements of these structures. The correlation between the material properties for different weight percentage mixtures of MWCNT, printing parameters and the mechanical properties like attaching forces, surface roughness and superhydrophobic nature are also identified with this study on bioinspired hierarchical structures.
ContributorsDwarampudi, Gana Sai Kiran Avinash Raj (Author) / Li, Xiangjia (Thesis advisor) / Ladani, Leila (Committee member) / Jin, Kailong (Committee member) / Arizona State University (Publisher)
Created2022
Description
Advancements in three-dimensional (3D) additive manufacturing techniques have opened up new possibilities for healthcare systems and the medical industry, allowing for the realization of concepts that were once confined to theoretical discussions. Among these groundbreaking research endeavors is the development of intricate magnetic structures that can be actuated through non-invasive methods, including electromagnetic and magnetic actuation. Magnetic actuation, in particular, offers the advantage of untethered operation. In this study, a photopolymerizable resin infused with Fe3O4 oxide nanoparticles is employed in the printing process using the micro-continuous liquid interface production technique. The objective is to optimize the manufacturing process to produce microstructures featuring smooth surfaces and reduced surface porosity, and enhanced flexibility and magnetic actuation. Various intricate structures are fabricated to validate the printing process's capabilities. Furthermore, the assessment of the flexibilty of these 3D-printed structures is conducted in the presence of an external magnetic field using a homemade bending test setup, allowing for a comprehensive characterization of these components. This research serves as a foundation for the future design and development of micro-robots using micro-continuous liquid interface production technique.
ContributorsJha, Ujjawal (Author) / Chen, Xiangfan (Thesis advisor) / Li, Xiangjia (Committee member) / Jin, Kailong (Committee member) / Nian, Qiong (Committee member) / Arizona State University (Publisher)
Created2023
Description
Both molecular structure of macromolecular materials and subsequent processing of these materials dictate resulting material properties. In this work novel synthetic strategies combined with detailed analytical methodology reveal fundamental structure-processing-property relationships in thermoplastic polyesters, thermoplastic polyurethanes, covalently crosslinked acetal functionalized networks, and small molecule surfactants. 4,4’ dimethyloxybisbenzoate afforded a series of novel polyester structures, and the incorporation of this monomer both increased the Tg and decreased the crystallinity in cyclohexane dimethanol based polyesters. Solubility and dynamic light scattering experiments combined with oscillatory rheology techniques provided methodology to validate polyurethane extrusion in commercial polyurethanes. Acid catalyzed hydroxyl addition to vinyl ethers provided two families of acetal functionalized poly(ethylene glycol hydrogels). Stoichiometric control of binary thiol-acrylate polymerizations afforded hydrogels with both tunable mechanical properties and predictable degradation profiles. Following this work, a photoacid generator catalyzed cationic catalysis provided acetal functionalized organogels whose mechanical properties were predicted by excess vinyl ether monomers which underwent cationic polymerization under the same reaction conditions that yielded acetal functionalization. Time resolved FT-IR spectroscopy provided new understanding in hydroxyl vinyl ether reactions, where both hydroxyl addition to a vinyl ether and vinyl ether cationic polymerization occur concurrently. This work inspired research into new reactive systems for photobase generator applications. However, current photobase generator technologies proved incompatible for carbon-Michael reactions between acetoacetate and acrylate functionalities as a result of uncontrollable acrylate free radical polymerization. The fundamental knowledge and synthetic strategies afforded by these investigations were applied to small molecule surfactant systems for fire-fighting applications. Triethylsilyl-containing zwitterionic and cationic surfactants displayed surface tensions lower than hydrocarbon surfactants, but larger than siloxane-containing surfactants. For the first time, oscillatory rheology and polarized optical light imagine rheology highlighted shear-induced micelle alignment in triethylsilyl surfactants, which provided more stable foams than zwitterionic analogues. The knowledge gained from these investigations provided fundamental structure-processing-property relationships in small molecule surfactant solutions applied as fire-fighting foams. This discovery regarding the effect of self-assembled structures in foam solutions informs the design and analysis of next generation surfactants to replace fluorocarbon surfactants in fire-fighting foam applications.
ContributorsBrown, James Robert (Author) / Long, Timothy E (Thesis advisor) / Bortner, Michael J (Committee member) / Biegasiewicz, Kyle F (Committee member) / Jin, Kailong (Committee member) / Arizona State University (Publisher)
Created2023
Description
Combining 3D bio-printing and drug delivery are promising techniques tofabricate scaffolds with well controlled and patient-specific structures for tissue
engineering. In this study, silk derivatives of bioink were developed consisting of
silk fibroin and gelatin then 3D printed into scaffolds. The scaffolds would be
evaluated for small molecule release, cell growth, degradation, and morphology.
Preparations and design of the scaffolds are major parts of engineering and tissue
engineering. Scaffolds are designed to mimic extracellular matrix by providing
structural support as well as promoting cell attachment and proliferation with
minimum inflammation while degrading at a controlled rate. Scaffolds offers new
potentials in medicine by aiding in the preparation of personalized and controlled
release therapeutic systems.
ContributorsNg, Johnny (Author) / Rege, Kaushal (Thesis advisor) / Holloway, Julianne (Committee member) / Jin, Kailong (Committee member) / Arizona State University (Publisher)
Created2022
Description
Polyolefins have dominated global polymer production for the past 60 years, revolutionizing fields of medicine, construction, travel, packaging, and many more. However, with steadily increasing polyolefin production each year and traditionally long polyethylene (PE) and polypropylene degradation times, estimated on the order of 500 years or more, a massive challenge arises with accumulating plastic waste. While the end-of-life of polyolefins previously manufactured must be addressed, incorporation of sustainability and circularity into future commodity plastic design at the molecular level offers an opportunity to decrease their negative effects on the environment going forward. Herein, several approaches are described which aim to address the need for polymeric materials while introducing a sustainable approach to their design, either through incorporation of biosynthesized polymers or degradable units. In the first project, polymer blends of two biodegradable polymers were studied, and compared to the same blends containing a graft copolymer compatibilizer comprised of the two homopolymer counterparts. The compatibilized blends were expected to have superior mechanical performance to the uncompatibilized blend and potentially offer industrially relevant benefits. While this was not achieved, valuable insight into the polymer blend interactions were gained. The idea of compatibilizing polymer blends was further explored with blends of PE and a cellulose derivative with the aid of a custom ABA triblock compatibilizing agent. It was discovered that the compatibilizer reinforced the polymer blend by providing mechanical strength at the cost of flexibility. To approach sustainability from a different perspective, several segmented copolymer series based on telechelic PE oligomers were then synthesized and analyzed. The segmented systems exhibited similar structure to high density PE (HDPE), retained similar mechanical and thermal properties to commercial HDPE, but contained degradable units throughout the polymer backbone. Several fundamental principles were explored through the segmented and chain-extended polyolefin architecture, including the influence of reactive linkage (amide vs. ester), random vs. alternating segment structure, and PE segment molecular weight. The effects of tailoring polymer structure on thermal, mechanical, and morphological properties are described herein. The relationships established from these experiments may further guide future polymer design and contribute toward more sustainable polyolefin manufacturing.
ContributorsArrington, Anastasia Sergeevna (Author) / Long, Timothy E. (Thesis advisor) / Jin, Kailong (Committee member) / Biegasiewicz, Kyle F. (Committee member) / Matson, John B. (Committee member) / Arizona State University (Publisher)
Created2022
Description
The objective of this research was to develop Aluminophosphate-five (AlPO4-5, AFI) zeolite adsorbents for efficient oxygen removal from a process stream to support an on-going Department of Energy (DOE) project on solar energy storage. A molecular simulation study predicted that substituted AlPO4-5 zeolite can adsorb O2 through a weak chemical bond at ambient temperature. Substituted AlPO4-5 zeolite was successfully synthesized via hydrothermal crystallization by following carefully designed procedures to tailor the zeolite for efficient O2 adsorption. Synthesized AlPO4-5 in this work included Sn/AlPO-5, Mo/AlPO-5, Pd/AlPO-5, Si/AlPO-5, Mn/AlPO-5, Ce/AlPO-5, Fe/AlPO-5, CuCe/AlPO-5, and MnSnSi/AlPO-5. While not all zeolite samples synthesized were fully characterized, selected zeolite samples were characterized by powder x-ray diffraction (XRD) for crystal structure confirmation and phase identification, and nitrogen adsorption for their pore textural properties. The Brunauer-Emmett-Teller (BET) specific surface area and pore size distribution were between 172 m2 /g - 306 m2 /g and 6Å - 9Å, respectively, for most of the zeolites synthesized. Samples of great interest to this project such as Sn/AlPO-5, Mo/AlPO-5 and MnSnSi/AlPO-5 were also characterized using x-ray photoelectron spectroscopy (XPS) and energy-dispersive x-ray spectroscopy (EDS) for elemental analysis, scanning electron microscopy (SEM) for morphology and particle size estimation, and electron paramagnetic resonance (EPR) for nature of adsorbed oxygen. Oxygen and nitrogen adsorption experiments were carried out in a 3-Flex adsorption apparatus (Micrometrics) at various temperatures (primarily at 25℃) to determine the adsorption properties of these zeolite samples as potential adsorbents for oxygen/nitrogen separation. Experiments showed that some of the zeolite samples adsorb little-to-no oxygen and nitrogen at 25℃, while other zeolites such as Sn/AlPO-5, Mo/AlPO-5, and MnSnSi/AlPO-5 adsorb decent but inconsistent amounts of oxygen with the highest observed values of about 0.47 mmol/ g, 0.56 mmol/g, and 0.84 mmol/ g respectively. The inconsistency in adsorption is currently attributed to non-uniform doping of the zeolites, and these findings validate that some substituted AlPO4-5 zeolites are promising adsorbents. However, more investigations are needed to verify the causes of this inconsistency to develop a successful AlPO4-5 zeolite-based adsorbent for oxygen/nitrogen separation.
ContributorsBuyinza, Allan Smith (Author) / Deng, Shuguang (Thesis advisor) / Varman, Arul M (Committee member) / Jin, Kailong (Committee member) / Arizona State University (Publisher)
Created2021
Description
Engineering polymers are critical for contemporary high-performance applications where toughness, thermal stability, and density are at a premium. These materials often demand high-energy processing conditions or highly reactive monomers that hold negative impacts on human and environmental health. Thus, this work serves to remediate the negative impacts of engineering polymer synthesis by addressing toxicity and processing at the monomer level, while maintaining or exceeding previous thermomechanical and stimuli-responsive performance. Polyurethanes (PUs) represent a class of engineering polymers that possess highly modular properties due to the diverse monomer selection available for their synthesis. The efficient reaction between isocyanates and hydroxyls impart stellar properties and flexible processing modalities, however recent scrutiny regarding the toxicity of the isocyanate precursors has driven the search for non-isocyanate polyurethane (NIPU) pathways. The advancement of bis-carbonylimidazolide (BCI) monomers for the synthesis of NIPU thermoplastics and foams is thoroughly investigated in this work. Remarkably, a novel decarboxylation pathway for BCI monomers controlled by catalyst loading enabled in-situ CO2 generation during crosslinking with trifunctional amines, and resulted in a facile synthetic route for NIPU foams. Further explorations into catalyst considerations revealed Dabco® 33-LV as a suitable mechanism for controlling reaction times and careful selection of surfactant concentration provided control over pore size and geometry. This led to a library of flexible and rigid NIPU foams that displayed a wide range of thermomechanical properties. Furthermore, sequestration of the imidazole byproduct through an efficient Michael reaction identified maleimide and acrylate additives as a viable pathway to eliminate post-processing steps resulting in NIPU foam synthesis that is amenable to current industrial standards. This route held advantages over the isocyanate route, as condensate removal drove molecular weight increase and ultimately achieved the first reported phase separation behavior of a NIPU thermoplastic containing a poly(ethylene glycol) soft segment. Furthermore, sustainable considerations for engineering polymers were explored with the introduction of a novel cyclobutane bisimide monomer that readily installs into various polymeric systems. Direct installation of this monomer, CBDA-AP-I, into a polysulfone backbone enabled controlled photo-cleavage, while further hydroxy ethyl functionalization allowed for incorporation into PU systems for photo-cleavable high-performance adhesive applications.
ContributorsSintas, Jose Ignacio (Author) / Long, Timothy E (Thesis advisor) / Sample, Caitlin S. (Committee member) / Jin, Kailong (Committee member) / Arizona State University (Publisher)
Created2024
GAS PERMEATION STUDIES OF THE COVALENT ORGANIC FRAMEWORKS (COFs) BASED MIXED MATRIX MEMBRANES (MMMs)
Description
Mixed Matrix Membranes (MMMs) combine a continuous organic polymer phase with a distributed porous additive, i.e. filler, and benefit from the ease processability of polymers as well as the improved gas separation performance of diverse porous filler materials. MMMs may have separation qualities that outperform the selectivity/permeability trade-off reported in pure polymer membranes. All MMMs require a polymer phase and a filler, and in this research a Pebax-1657 is used as a matrix and for filler a Covalent organic framework (COF) as it is less understood. Covalent organic frameworks (COFs) represent a category of porous organic polymers that have garnered significant interest across various fields, including gas adsorption and storage, catalysis, sensing, and photovoltaics. These frameworks offer outstanding characteristics such as permanent porosity, high surface areas, and easily adjustable frameworks [3]. Additionally, their entirely organic composition can lead to enhanced interactions between fillers and polymers, mitigating the formation of nonselective defects during mixed-matrix membrane (MMM) preparation that are often seen with using other sorts of fillers such as silica and metal- organic frameworks (MOFs). Once synthesized the MMMs which are based on COF will be tested in an in house built gas permeance setup to test for single gas permeance, giving us deep insight into the performance of the COF bas MMMs.
ContributorsTomar, Dhruv Singh (Author) / Jin, Kailong (Thesis director) / Lopez, Jose (Committee member) / Barrett, The Honors College (Contributor) / Chemical Engineering Program (Contributor)
Created2024-05
Description
In this report, a PDMS network formed from catalysis of a linear, bifunctional polymer by Ashby-Karstedt’s catalyst is analyzed. An exploration of the crosslink density, shear plateau modulus, and glass transition temperature is performed to display some of the material’s mechanical, chemical, and thermal properties. The softness of this network in addition to the biocompatibility and thermal stability of PDMS make this elastomer useful for a broad spectrum of applications.
ContributorsEnos, Emma (Author) / Jin, Kailong (Thesis director) / Self, Jeffrey (Committee member) / Barrett, The Honors College (Contributor) / Chemical Engineering Program (Contributor)
Created2024-05