Tailoring the surface of nanoparticles is essential for biological applications of magnetic nanoparticles. FePt nanoparticles are interesting candidates owing to their high magnetic moment. Established procedures to make FePt nanoparticles use oleic acid and oleylamine as the surfactants, which make them dispersed in nonpolar solvents such as hexane. As a model study to demonstrate the modification of the surface chemistry, stable aqueous dispersions of FePt nanoparticles were synthesized after ligand exchange with mercaptoalkanoic acids. This report focuses on understanding the surface chemistry of FePt upon ligand exchange with mercapto compounds by conducting X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR) studies. It was found that the mercapto end displaces oleylamine on the Pt atoms and the carboxylic acid end displaces the oleic acid on the Fe atoms, thus exposing carboxylate and thiolate groups on the surface that provide the necessary electrostatic repulsion to form stable aqueous dispersions of FePt nanoparticles.
The IMC−PID tuning rules demonstrate good set-point tracking but sluggish disturbance rejection, which
becomes severe when a process has a small time-delay/time-constant ratio. In this study, an optimal internal
model control (IMC) filter structure is proposed for several representative process models to design a
proportional−integral−derivative (PID) controller that produces an improved disturbance rejection response.
The simulation studies of several process models show that the proposed design method provides better
disturbance rejection for lag-time dominant processes, when the various controllers are all tuned to have the
same degree of robustness according to the measure of maximum sensitivity. The robustness analysis is
conducted by inserting a perturbation in each of the process parameters simultaneously, with the results
demonstrating the robustness of the proposed controller design with parameter uncertainty. A closed-loop
time constant λ guideline is also proposed for several process models to cover a wide range of θ/τ ratios.
This paper is primarily focused in studying the effects of nanoclay particles such as montmorillonite on improving mechanical and thermal properties of fiber reinforced polymer matrix composite materials. Basic correlations between polymer morphology, strength, modulus, toughness, and thermal stability of thermoset nanocomposites were investigated as a function of layered silicate content. S2-glass/epoxy-clay nanocomposites were manufactured through an affordable vacuum assisted resin infusion method (VARIM). The nanocomposites are formed during polymerization when the adsorbing monomer separates the clay particles into nanometer scales. Transmission electron microscopy (TEM) and wide angle X-ray diffraction(WAXD) were used to characterize the morphology of the dispersed clay particles. The thermal properties such as onset of decomposition and glass transition temperatures were determined by Thermo Gravimetric Analysis (TGA) and Dynamic Modulus Analyzer (DMA). Mechanical properties such as interlaminar shear strength, flexural properties and fracture toughness are also determined for both conventional S2-glass/epoxy composites and S2-glass fiber reinforced nanocomposites. The results show significant improvements in mechanical and thermal properties of conventional fiber reinforced composites with low loading of organo silicate nanoparticles. By dispersing 1% by weight nanosilicates, S2-glass/epoxy-clay nanocomposites attributed to almost 44, 24 and 23% improvement in interlaminar shear strength, flexural strength and fracture toughness in comparison to conventional S2-glass/epoxy composites. Similarly, the nanocomposites exhibit approximately 26 C higher decomposition temperatures than that of conventional composites. This improved properties of fiber reinforced polymer nanocomposites are achieved mostly due to increased interfacial surface areas, improved bond characteristics and intercalated/exfoliated morphology of the epoxy-clay nanocomposites. The TEM observations provide evidence of detailed morphology of the polymer layered-clay nanocomposites.
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