Philip Costanzo

Thermal-initiated hydroxyethyl methacrylate functionalization of multiwalled carbon nanotubes

Greg Curtzwiler et al. — Thu, 25 Aug 2011 16:02:10 PDT

Multiwalled-carbon nanotubes (MWCNTs) were functionalized via thermoinitiated free radical polymerization of 2-hydroxyethyl methacrylate (HEMA) using benzoyl peroxide. Tip sonication was used during the polymerization reaction to separate agglomerated nanotubes. The functionalization was confirmed by control experiments and attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR). Differential scanning calorimetry indicated that the addition of poly(HEMA)-MWCNTs to a two-component polyurethane coating will have little effect on the glass transition temperature of the coating. The poly(HEMA)-functionalized MWCNTs formed large colloidal structures of highly dispersed nanotubes in both the nonsheared and sheared coatings as determined by atomic force microscopy. This study determined a quick and easy method to functionalize MWCNTs for incorporation into a two-component polyurethane coating. A simple method for producing ordered structures of the MWCNTs via shear observed.

Calorimetric Study of Block-Copolymers of Poly(n-butyl acrylate) and Gradient Poly(n-butyl acrylate-co-methyl methacrylate)

A I. Buzin et al. — Fri, 29 Oct 2010 17:07:04 PDT

The nanophase separation in diblock and triblock copolymers consisting of immiscible poly(n-butyl acrylate) (block A) and gradient copolymers of methyl methacrylate (MMA) and n-butyl acrylate (n BA) (block M/A) were investigated by means of their heat capacity, C_p, as a function of the composition of the blocks M/A and temperature. In all copolymers studied, both blocks are represented by their C_p and glass transition temperature, T_g, as well as the broadening of the transition-temperature range. The low-temperature transition of the blocks A is always close to that of the pure poly(n-butyl acrylate) and is independent of the analyzed compositions of the block copolymer, but broadened asymmetrically relative to the homopolymer due to the small phase size. The higher transition is related to the glass transition of the copolymer block of composition M/A. Besides the asymmetric broadening of the transition due to the phase separation, it decreases in T_g and broadens, in addition, symmetrically with increasing acrylate content. The concentration gradient is not able to introduce a further phase separation with a third glass transition inside the M/A block.

Biomolecule Detection via Target Mediated Nanoparticle Aggregation and Dielectrophoretic Impedance Measurement

Philip J. Costanzo et al. — Fri, 29 Oct 2010 17:07:02 PDT

A new biosensing system is described that is based on the aggregation of nanoparticles by a target biological molecule and dielectrophoretic impedance measurement of these aggregates. The aggregation process was verified within a microchannel via fluorescence microscopy, demonstrating that this process can be used in a real time sensor application. Positive dielectrophoresis is employed to capture the nanoparticle aggregates at the edge of thin film electrodes, where their presence is detected either by optical imaging via fluorescence microscopy or by measuring the change in electrical impedance between adjacent electrodes. The electrical detection mechanism demonstrates the potential for this method as a micro total analysis system (mTAS).