2,979 research outputs found

    Research on aseismic behavior of assemble-type composited wall

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    Synthesis and Characterization of a Novel Polyacetal & Design and Preparation of Superhydrophobic Photocatalytic Surfaces

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    Polyacetal polymers are thermoplastic resins that play an important role in industry because of numerous industrial applications including automobile; household appliance; etc. The first part of this thesis (Chapter 2) is about the synthesis of a new acetal copolymer that exhibits superior thermal stability. The second part of this thesis (Chapter 3) is about the preparation and applications of TiO2-based polymer nanocomposite films, where the reactive oxygen species (ROS) are generated on the solid surface. Catalytic nanocomposite films are an active area of research because of their potential uses for environmental remediation and chemical synthesis. Furthermore, to enhance surface functionality, superhydrophobic surfaces are prepared using catalyst particles, where the ROS could be generated at the solid-liquid-gas interphase. These works are presented in the third part of this thesis (Chapters 4 and 5). Acetal copolymers represent a family of well-established engineering thermoplastics serving a broad range of important industrial applications including replacement for metals. Their structure consists of oxymethylene units with a low concentration of co-monomer units. By interrupting the facile hemiacetal hydrolysis reaction that can propagate along the macromolecular chain, these co-units function as a stopper against degradation of the main block, -(CH2O)n-. The copolymer can also be blended with additives such as stabilizers and reinforcements more easily than the homopolymer due to more flexible polymer chains. Previous approaches have incorporated the stopper through cationic copolymerization of cyclic acetals such as ethylene oxide, dioxolane and dioxepane. The first part of this thesis describes the first synthesis of an eight-member ring acetal, 6-methyl-1, 3-dioxocane (MDOC), and its cationic copolymerization with trioxane initiated by boron trifluoride dibutyl etherate. The copolymerization process was monitored in situ using proton NMR. Incorporation of MDOC led to the insertion of the stopper unit, -[CH2CH2CH(CH3)CH2CH2)O]- , thus synthesizing the new acetal copolymer. A superior copolymer thermal stability with a ~ 20°C increase in degradation onset temperature compared with end-capped polyoxmethylene was observed. Both TGA and DSC data indicated the random placement of the stopper in the copolymer likely due to efficient transacetalization because of the higher basicity and flexibility of the stopper unit compared with co-units comprising 2 to 4 carbons in length. DSC thermo-grams showed a melting curve of a polymer with melting point lower, as expected, than that of oxymethylene homopolymer. No homopolymer in the copolymer samples was in indicated by TGA. The new acetal copolymer, poly(6-methyl-1,3-dioxocane-co-trioxane), which has a stopper co-unit with five carbon atoms along the backbone, contains the longest reported stopper co-unit, potentially leading to improved elongation, and toughness and better compatibility with a range of additives compared to acetal homopolymers. The second part of this thesis is focused on the design and preparation of photocatalytic surfaces. The use of TiO2 as a semiconducting heterogeneous photocatalyst for the photodegradation of organic pollutants has been extensively investigated as the material is non-toxic, inexpensive, and chemically stable over a wide pH range. Chapter 3 presents a novel lamination fabrication method that enables pre-formed TiO2 nanoparticles to become partially embedded in the surface of a thermoplastic polymer film. In this way, the particles are strongly adhered to the surface while remaining accessible to the aqueous solution. By modifying the fabrication conditions (e.g. temperature, pressure, polymer melt viscosity, etc.), the morphology of the hierarchical TiO2-polymer surface can be controlled and thus the rate of photocatalytic reactions can be increased. In addition, the fraction of TiO2 particles that become fully embedded in the polymer surface, and so inaccessible to photocatalysis reactions, can be reduced through lamination process control, thereby reducing costs. Nanocomposite films were characterized (XPS, SEM, AFM, TGA) and tested by photooxidizing a Rhodamine B solution under either a UV lamp or natural sunlight. The morphology of the surface was correlated with both fabrication conditions and photocatalysis rate. This environmentally friendly technique is compatible with any type of TiO2 catalyst particle and so the wavelength response of the photocatalysis can be improved as particles that retain photocatalytic activity at longer wavelengths become commercially available. The wide variety of thermoplastic polymers that are compatible with the process will facilitate their introduction into a wide range of applications including waste water treatment and water purification. In Chapter 4 and Chapter 5, a general approach is presented to incorporating particles into a superhydrophobic surface that catalyze the formation of reactive oxygen species. Superhydrophobic photocatalytic surfaces are prepared using hydrophilic TiO2 nanoparticles and hydrophobic Silicon-Phthalocyanine photosensitizer particles. A stable Cassie state was maintained, even on surfaces fabricated with hydrophilic TiO2 particles, due to significant hierarchical roughness. A triple phase photogenerator is designed and fabricated. By printing the surface on a porous support, oxygen could be flowed through the plastron resulting in significantly higher photooxidation rates relative to a static ambient. Photooxidation of Rhodamine B and BSA were studied on TiO2-containing surfaces and singlet oxygen was trapped on surfaces incorporating Silicon-Phthalocyanine photosensitizer particles. Catalyst particles could be isolated in the plastron to avoid contamination by the solution. This approach may prove useful for water purification and medical devices where isolation of the catalyst particle from the solution is necessary and so Cassie stability is required

    Measuring CEO Talent and Its Impact on Firm Performance: A Theoretical Integration and Empirical Analysis

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    This paper analyzes whether CEOs who are good contrarian investors, good forecasters, or good market timers can run their firms better. Besides using the timing measure which combines returns before and after the trade, we also use the past return measure to estimate the contrarian aspect of CEO trades and the future return measure to assess CEO’s ability to forecast stock returns. Our results suggest that CEOs’ managerial talent and valuation ability are primarily related to CEOs’ past return measure, while high post-trade returns indicate the expropriation motive for CEO trades. Overall, we obtain strong evidence to support the idea that CEOs who are good contrarian investors tend to run their firms better on average than other CEOs

    A deep learning approach to solve forward differential problems on graphs

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    We propose a novel deep learning (DL) approach to solve one-dimensional non-linear elliptic, parabolic, and hyperbolic problems on graphs. A system of physics-informed neural network (PINN) models is used to solve the differential equations, by assigning each PINN model to a specific edge of the graph. Kirkhoff-Neumann (KN) nodal conditions are imposed in a weak form by adding a penalization term to the training loss function. Through the penalization term that imposes the KN conditions, PINN models associated with edges that share a node coordinate with each other to ensure continuity of the solution and of its directional derivatives computed along the respective edges. Using individual PINN models for each edge of the graph allows our approach to fulfill necessary requirements for parallelization by enabling different PINN models to be trained on distributed compute resources. Numerical results show that the system of PINN models accurately approximate the solutions of the differential problems across the entire graph for a broad set of graph topologies.Comment: 40 pages, 27 figure

    Exploring the partonic collectivity in small systems at the LHC

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    Using the Hydro-Coal-Frag model that combines hydrodynamics at low pTp_{\rm T}, quark coalescence at intermediate pTp_{\rm T}, and the LBT transport model at high pTp_{\rm T}, we study the spectra and elliptic flow of identified hadrons in high multiplicity p--Pb and p--p collisions at the Large Hadron Collider (LHC). In p--Pb collisions, the Hydro-Coal-Frag model gives a good description of the differential elliptic flow over the pTp_{\rm T} range from 0 to 6 GeV and the approximate number of constituent quark (NCQ) scaling at intermediate pTp_{\rm T}. Although Hydro-Coal-Frag model can also roughly describe the elliptic flow in high multiplicity p--p collisions with the quark coalescence process, the larger contribution from the string fragmentations leads to a notable violation of the NCQ scaling of v2v_2 at intermediate pTp_{\rm T} as observed in the experiment. Comparison runs of the Hydro-Frag model without the coalescence process demonstrate that regardless the parameter adjustments, the Hydro-Frag model cannot simultaneously describe the pTp_{\rm T} spectra and the elliptic flow of identified hadrons in either p--Pb collisions or p--p collisions. The calculations in this paper thus provide support for the existence of partonic degrees of freedom and the possible formation of the QGP in the small systems created at the LHC.Comment: 9 pages, 3 figure
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