Nanoparticles

Over the past decade, hydrogen gas generation has been a critical component toward clean energy due to its high specific energy content. Generating hydrogen gas from water is crucial for future applications, including space transportation. Recent studies show promising results using silicon nanoparticles (SiNPs) for spontaneous hydrogen generation, but most methods require external energy like high temperature or pressure. In this work, we investigated hydrogen production from SiNPs without external energy by leveraging high pH water using sodium hydroxide and optimizing the process with a microfluidic approach. When comparing the physical dispersion methods using the 0.1 mg/mL case, ultrasonic bath produced more hydrogen than magnetic stirrer. In this thesis, 0.01% dextran with pure SiNPs at concentrations of 0.1 mg/mL, 0.2 mg/mL, and 0.3 mg/mL was analyzed. The highest concentration with dextran generated at least 40% less hydrogen than silicon alone, thus dextran did not increase hydrogen gas.

Due to technological advancement, energy consumption and demand have been increasing significantly, primarily satisfied by fossil fuel consumption. This reliance on fossil fuels results in substantial greenhouse gas emissions, with CO₂ being the most prominent contributor to global warming. To mitigate this issue and prevent CO₂ emissions, Carbon Capture, Utilization, and Storage (CCUS) technologies are employed. Among these, the amine scrubbing method is widely used due to its high CO2 capture efficiency and regenerative ability. However, this method has drawbacks, including high toxicity, corrosion, and substantial freshwater consumption.
To develop an environmentally sustainable carbon capture solution, researchers are exploring alternatives such as the use of seawater and enhanced CO2 capture with catalysts. In this study, we analyze the catalytic performance of nickel nanoparticles (NiNPs) in seawater with carboxymethyl cellulose (CMC) polymers. Using flow-focusing geometry-based microfluidic channels, we investigated CO₂ dissolution at various concentrations of nanoparticles and CMC polymers. The objective is to optimize the concentration of nanoparticles and CMC polymers for effective CO₂ dissolution. We utilized NiNPs with diameters of 100 nm and 300 nm in CMC concentrations of 100 ml/L, 200 ml/L, and 300 ml/L. Additionally, NiNP concentrations ranging from 6 mg/L to 150 mg/L were tested for CO₂ dissolution in seawater. The results indicated that a concentration of 10 mg/L NiNPs in 100 mg/L CMC provided a CO₂ dissolution of 57%, the highest for this specific CMC concentration. At CMC concentrations of 200 ml/L and 300 ml/L, NiNP concentrations of 70 mg/L and 90 mg/L achieved CO₂ dissolution rates of 58.8% and 67.2%, respectively.

Prostate cancer (PCa) is the second most diagnosed cancer in men. The resistance of prostate cancer to chemotherapy has been linked to the ATP Binding Cassette (ABC)-Mediated Multidrug Resistance (MDR). This study investigated the combination of 3-Bromopyruvate (3-BPA) and the anti-inflammatory molecule SC-514 in reducing MDR in prostate cancer. The compounds were incorporated into a PLGA nanoparticles to increase delivery to target cells.
To investigate the effectiveness of SC-514 and/3-BPA, cytoxicity assays including trypan blue dye exclusion, MTT tetrazolium reduction, NBT, LDH release poly caspase detection, cell titer glow assay, and ELISA were utilized. Both immunofluorescence and multidrug resistance efflux assays were utilized to estimate the number of drug resistant cells. SC-514 was encapsulated in PLGA nanoparticles via single-emulsion method. SC-514 nanoparticles were analyzed utilizing Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM). Liquid chromatography–mass spectrometry (LC–MS) was used to measure the amount of SC- 514 released from the nanoparticle. Alternative SC-514 drug release quantification methods such as colony forming assay, wound healing assay, and transwell and migration assay were explored.

This thesis reports the development of a novel drug delivery system consisting of hollow nanoparticles, formed from manganese dioxide (δ-MnO2) sheets, that are coated with polydopamine and folic acid to selectively target cancer cells. The biodegradability and colloidal stability of the uncoated hollow nanoparticles were investigated in comparison to solid MnO2 nanoparticles and graphene oxide sheets. The MnO2 hollow nanoparticles degraded at a faster rate and seem to have a higher surface area and better colloidal dispersion than solid MnO2 nanoparticles. Xanthan gum was proven to improve colloidal dispersion of these hollow nanoparticles and were used for further cell studies. In this study, cancer and healthy cells were treated with coated hollow nanoparticles, and results indicate that this novel hollow nanoparticle may preferentially target and kill cancer cells. Particle aggregation has shown to be toxic to cells. Further studies with this novel drug delivery system may lead to a groundbreaking solution to targeted cancer therapy.

The Supported red blood cell membrane (SRBCm) was developed on a piezoelectric sensor to study the attachment of nanoparticles to erythrocyte surfaces. A well-dispersed colloidal suspension of fragments of RBCm was prepared from whole blood, and characterized thoroughly using cryogenic transmission electron microscopy, dynamic light scattering, and zeta potential analysis. To develop SRBCm, RBCm fragments were immobilized onthe sensor in a quartz crystal microbalance with dissipation monitoring system. A complete monolayer of flattened fragments of RBCm was formed on the positively charged surface of the piezoelectric sensor in 1 mM NaCl and 0.2 mM NaHCO3 at pH 7.1. The surface morphology of SRBCm was characterized via atomic force microscopy. The even distribution of surface proteins expressed on erythrocytes was found on SRBCm through indirect immunofluorescence microscopy. The attachment efficiencies of model nanoparticles, e.g. hematite nanoparticles and carboxylated polystyrene nanoparticles, on the SRBCm were quantified using a classic methodology.
KEYWORDS: Supported erythrocyte membrane, piezoelectric sensor, phospholipid bilayers, nanoparticles

Core-shell nanohybrids have wide applications in pollutant degradation. In this study, core-shell nanohybrid was formed through heteroaggregation between neutral nanoparticles (i.e., hematite nanoparticles or HemNPs) and charged nanoparticles (i.e., carboxylated polystyrene nanoparticles or PSNPs). In the dispersant solution of 1 mM NaCl at pH 6.3, HemNPs were neutral and underwent favorable homoaggregation, whereas PSNPs were negatively charged and underwent no homoaggregation. When the two types of particles were mixed, homoaggregation of HemNPs and heteroaggregation between HemNPs and PSNPs took place simultaneously, forming HemNPs-PSNPs heteroaggregates. The transmission electron microscopy images of heteroaggregates show that HemNPs and PSNPs formed core-shell structure in which HemNPs were the cores and PSNPs were the shells. The size of the core-shell nanohybrids can be controlled by varying the concentration ratio of HemNPs to PSNPs. The increase of the size of charged nanoparticles resulted in larger nanohybrids. This new method has lower energy footprint than existing ones.

Nano-reinforced polymeric systems have demonstrated a great deal of interest
within academia and industry, due to the intrinsic properties of the graphene nanofillers,
having excellent mechanical, thermal and electrical properties. The reinforcement of multiwall
carbon nanotubes (MWCNTs) and graphene nanoplatelets (GNPs) were introduced
into a low cost, non-carcinogenic, high temperature PMR type polyimide resin. The effects
of the interfacial interaction and dispersion quality resulted in improvement in the glass
transition temperature (Tg), elastic modulus and thermal stability by, 31°C, 63% and 16°C,
respectively. In fine, this study presents a simple but effective high temperature polyimide
(HTPI) nanocomposites manufacturing procedure and established that nanoparticle
reinforcement can be used to improve both thermal and mechanical properties.

A novel approach has been introduced in making flexible armor composites. Armor composites are usually made by reinforcing Kevlar fabric into the mixture of a polymer and nanoscale particles. The current procedure deviates from the traditional shear thickening fluid (STF) route and instead uses silane (amino-propyl-trimethoxy silane) as the base polymer. In addition, a cross-linking fixative such as Glutaraldehyde (Gluta) is added to the polymer to create bridges between distant pairs of amine groups present in Kevlar and silated nanoparticles. Water, silane, nanoparticles and Gluta are mixed using a homogenizer and an ultra-sonochemical technique. Subsequently, the admixture is impregnated with Kevlar - bypassing the heating and evaporating processes involved with STF. The resulting composites have shown remarkable improvement in spike resistance; at least one order higher than that of STF/Kevlar composites. The source of improvement has been traced to the formation of secondary amine C-N stretch due to the presence of Gluta.