Temperature-dependent electrical resistance of conductive polylactic acid filament for fused deposition modeling

This study characterizes the microstructure and temperature dependence of resistance of two commercially available electrically conductive polylactic acid (PLA) composites for fused deposition modeling (FDM): PLA-carbon black and PLA-graphene. No microstructural changes were observed between the filament and the printed parts; however, the resistivity of the filament was found to drop by four to six times upon FDM. Also, compared to the resistivity of individual extruded wire, the resistivity of the printed parts was found to be up to 1500 times higher for PLA-graphene and up to 300 times higher for PLA-carbon black. The raw PLA-carbon black filament and printed wire showed a positive temperature coefficient of resistance (α) value between ~?0.03 and 0.01 °C^?1, which makes them more suitable for sensor development. The raw PLA-graphene filament and printed wire did not exhibit a significant α, which makes them more suitable for printing wires. However, the parts made with multilayer FDM exhibited a negative or a negligible α up to a certain temperature prior to exhibiting a positive α; further, these α values were significantly lower than those obtained for the filaments before or after extrusion. These findings enable proper selection of commercial conductive FDM filaments for enabling quicker prototyping of electronics and sensors.     

Control of Nanoscale Environment to Improve Stability of Immobilized Proteins on Diamond Surfaces

Immunoassays for detection of bacterial pathogens rely on the selectivity and stability of bio-recognition elements such as antibodies tethered to sensor surfaces. The search for novel surfaces that improve the stability of biomolecules and assay performance has been pursued for a long time. However, the anticipated improvements in stability have not been realized in practice under physiological conditions because the surface functionalization layers on commonly used substrates, silica and gold, are themselves unstable on time scales of days. In this paper, we show that covalent linking of antibodies to diamond surfaces leads to substantial improvements in biological activity of proteins as measured by the ability to selectively capture cells of the pathogenic bacterium Escherichia coli O157:H7 even after exposure to buffer solutions at 37 °C for extended periods of time, approaching 2 weeks. Our results from ELISA, XPS, fluorescence microscopy, and MD simulations suggest that by using highly stable surface chemistry and controlling the nanoscale organization of the antibodies on the surface, it is possible to achieve significant improvements in biological activity and stability. Our findings can be easily extended to functionalization of micro and nanodimensional sensors and structures of biomedical diagnostic and therapeutic interest.     

Micromachined GC columns for fast separation of organophosphonate and organosulfur compounds

This article demonstrates how to prepare microfabricated columns (microcolumns) for organophosphonate and organosulfur compound separation that rival the performance of commercial capillary columns. Approximately 16,500 theoretical plates were generated with a 3 m long OV-5-coated microcolumn with a 0.25 microm phase thickness using helium as the carrier gas at 20 cm/s. Key to the advance was the development of deactivation procedures appropriate for silicon microcolumns with Pyrex tops. Active sites in a silicon-Pyrex microcolumn cause peak tailing and unwanted adsorption. Experimentally, we found that organosilicon hydride deactivation lowers adsorption activity in microcolumns more than silazane and silane treatments. But without further treatment, the phosphonate peaks continue to tail after the coating process. We found that heat treatment with pinacolyl methylphosphonic acid (PMP) eliminated the phosphonate peak tailing. In contrast, conventional resilylation employing N, O-bis(trimethylsilyl)acetamide, hexamethyldisilazane, and 1-(trimethylsilyl)imidazole does not eliminate peak tailing. Column activity tests show that the PMP treatment also improves the peaks for 2,6-dimethyl aniline, 1-octanol, and 1-decanol implying a decrease in the column's hydrogen bonding sites with the PMP treatment. FT-IR analysis shows that exposure to PMP forms a bond to the stationary phase that deactivates the active sites responsible for organophosphonate peak tailing.     

Development of geopolymer composites for EMI shielding from steel industry waste

Journal of Materials Science: Materials in Electronics - In this study waste from steel industries, namely, mill scale, red dust, and iron ore fines have been used as additives in geopolymer matrix...     

Nitrogen-doped carbon dots from Kraft lignin waste with inorganic acid catalyst and their brain cell imaging applications

Carbon quantum dots (C-QDs) show potential to replace traditional semiconductive quantum dots as the next generation of fluorescent probes. We demonstrate here a new C-QD production process using lignin, a high-volume but low market-value industrial waste and/or environmental hazards, as the starting carbon source. By adding a small amount of inorganic acid, the rich phenolic components in lignin were successfully converted to C-QDs through a coking formation mechanism similar to what happens on solid acid catalysts in traditional fossil fuel cracking process. Their aqueous solution presence of the received lignin C-QDs is beneficial for brain cell imaging applications, attributing to their fast internalization, low toxicity, tunable photoluminescence by appropriate acidity and reaction temperature during hydrothermal synthesis. This method not only provides a low-cost C-QDs production route, but also helps gain extra profit and/or improve environment for many small agricultural business and paper and pulp industry located in rural area.     

Biosensors: Control of Nanoscale Environment to Improve Stability of Immobilized Proteins on Diamond Surfaces (Adv. Funct. Mater. 6/2011)

Immunoassays for detection of bacterial pathogens rely on the selectivity and stability of bio‐recognition elements such as antibodies tethered to sensor surfaces. The search for novel surfaces that improve the stability of biomolecules and assay performance has been pursued for a long time. However, the anticipated improvements in stability have not been realized in practice under physiological conditions because the surface functionalization layers on commonly used substrates, silica and gold, are themselves unstable on time scales of days. In this paper, we show that covalent linking of antibodies to diamond surfaces leads to substantial improvements in biological activity of proteins as measured by the ability to selectively capture cells of the pathogenic bacterium Escherichia coli O157:H7 even after exposure to buffer solutions at 37 ºC for extended periods of time, approaching 2 weeks. Our results from ELISA, XPS, fluorescence microscopy, and MD simulations suggest that by using highly stable surface chemistry and controlling the nanoscale organization of the antibodies on the surface, it is possible to achieve significant improvements in biological activity and stability. Our findings can be easily extended to functionalization of micro and nanodimensional sensors and structures of biomedical diagnostic and therapeutic interest.     

Synergistic effect of Mill scale and MoS2 in geopolymer composites for EMI shielding application

Journal of Materials Science: Materials in Electronics - This study reports the development of a synergistic composition of geopolymer for EMI shielding building material using micron-sized...