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O'Bryan, Greg

Publications and source records attributed to O'Bryan, Greg.

At least 19 records

Surface treatment of ultra-high molecular weight polymers

The methods and compounds disclosed herein relate to the surface modification of UHMWPs by means of a catalytic C—H bond insertion catalyst using a rhodium catalysts in conjunction with carbene-generating diazo compounds. The catalytic treatment imparts covalently added functionality to the UHMWPE surface. This functionality acts as an excellent grafting mechanism for grafting, bonding, or adhering further materials to the UHMWPs surface.

O'Bryan, Greg↗

An Efficient Post-Polymerization Modification of Poly(Styrene- co -Maleic Anhydride) for Thermally Reversible Nanocomposites

A copolymer of maleic anhydride and styrene is functionalized with Diels–Alder (DA) capable pendant groups to enable the study of this material with different crosslink densities. This constituent is synthesized using commercially available starting materials and relatively simple and uncomplicated chemistries which open the possibility for its use in large-scale applications. The 10%, 25%, 50%, and 100% DA nominal crosslinking based on available pendant furan groups on the polymeric component is investigated. The reaction kinetics are monitored using infrared spectroscopy and rheology. Based on the rheological results, carbon nanotube (CNT) incorporation into the DA matrix is explored in order to determine its effects on the complex modulus of the material. This work done in this report is meant as a proof of concept for this DA material with the possibility of its incorporation into other commonly used bulk materials and/or adhesives to allow for an easily reversible product formulation.

36 MATERIALS SCIENCE↗

Covalent Surface Modifications of Carbon Nanotubes.

A report meant to document the chemistries investigated by the author for covalent surface modification of CNTs. Oxidation, cycloaddition, and radical reactions were explored to determine their success at covalently altering the CNT surface. Characterization through infrared spectroscopy, Raman spectroscopy, and thermo gravimetric analysis was performed in order to determine the success of the chemistries employed. This report is not exhaustive and was performed for CNT surface modification exploration as it pertains to the "Next Gen" project.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Tailoring next-generation biofuels and their combustion in next-generation engines

Increasing energy costs, the dependence on foreign oil supplies, and environmental concerns have emphasized the need to produce sustainable renewable fuels and chemicals. The strategy for producing next-generation biofuels must include efficient processes for biomass conversion to liquid fuels and the fuels must be compatible with current and future engines. Unfortunately, biofuel development generally takes place without any consideration of combustion characteristics, and combustion scientists typically measure biofuels properties without any feedback to the production design. We seek to optimize the fuel/engine system by bringing combustion performance, specifically for advanced next-generation engines, into the development of novel biosynthetic fuel pathways. Here we report an innovative coupling of combustion chemistry, from fundamentals to engine measurements, to the optimization of fuel production using metabolic engineering. We have established the necessary connections among the fundamental chemistry, engine science, and synthetic biology for fuel production, building a powerful framework for co-development of engines and biofuels.

09 BIOMASS FUELS↗

Triblock polymers for nanoporous membranes

The fabrication of nanoporous thin-film membranes from block polymers is proposed. A computational modeling effort is described, which optimizes the polymer block lengths in order to obtain thermodynamically favorable phase-separated morphologies. Synthetic rout es to access poly(ethylene oxide) and poly (methyl methacrylate)-based block polymers are outlined. These materials were then prepared using controlled free rad ical polymerization. The relative advantages and disadvantages of numerous routes are discussed. Characterization of di- and triblock polymers using nuclear magnetic resonance spectroscopy and size-exclusion chromatograph revealed less than ideal re-initiation and cha in growth o f macroinitiators. Preliminary phase-behavior of these materials is reported from small angle x-ray scattering and scanning electron microscopy.

Cordaro, Joseph Gabriel↗