ABSTRACT
Magnetic properties of undoped anatase, rutile, and amorphous titanium dioxide (TiO2) nanotubes grown by electrochemical anodization were studied by superconducting quantum interference device (SQUID) and electron spin resonance (ESR) methods in the temperature range 1.8-300 K. All anatase, rutile, and amorphous TiO2 nanotubes were found to exhibit paramagnetic behaviors in the entire temperature range when tested with magnetic center concentrations of 6×10(17), 3×10(16), and 3 × 10(15) cm(-3), respectively. The diameter of the TiO2 nanotubes varied from 40-160 nm and has no significant effect on the magnetic properties observed. SQUID data showed strong nonlinear M-H relationships for anatase at low temperatures, and Arrot plot analysis suggested ferromagnetism in the sample with a Curie temperature T(C) ~ 6 K. However, ESR studies showed no evidence for long-distance magnetic ordering. ESR studies revealed two magnetic centers with g1 = 1.928 and g2 = 2.028 that were common to all samples. The resonance peak at g1 = 1.922 was ascribed to Ti(3+) cations centers resulting from oxygen vacancies, while the peak at g2 = 2.028 was ascribed to surface absorbents. The amorphous sample ESR spectrum contained additional resonance peaks with corresponding g values at 2.228, 1.873, and 1.715 that possibly resulted from the disordered nature of these samples.
ABSTRACT
We present a plastic microfluidic device with integrated nanoscale magnetic traps (NSMTs) that separates magnetic from non-magnetic beads with high purity and throughput, and unprecedented enrichments. Numerical simulations indicate significantly higher localized magnetic field gradients than previously reported. We demonstrated >20 000-fold enrichment for 0.001% magnetic bead mixtures. Since we achieve high purity at all flow-rates tested, this is a robust, rapid, portable, and simple solution to sort target species from small volumes amenable for point-of-care applications. We used the NSMT in a 96 well format to extract DNA from small sample volumes for quantitative polymerase chain reaction (qPCR).
