26.11.2012 Views

Materials Science and Engineering Laboratory FY 2004 ... - NIST

Materials Science and Engineering Laboratory FY 2004 ... - NIST

Materials Science and Engineering Laboratory FY 2004 ... - NIST

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

Executive Summary<br />

The <strong>NIST</strong> homepage summarizes the key vision for<br />

the National Institute of St<strong>and</strong>ards <strong>and</strong> Technology<br />

. . .working with industry to foster innovation, trade,<br />

security <strong>and</strong> jobs. This vision guides the choices of<br />

research in the Polymers Division. In this annual<br />

report, we have tried to give you an update on our<br />

current projects <strong>and</strong> a glimpse of some of the<br />

scientific highlights of <strong>2004</strong>.<br />

Our researchers supporting the electronics materials<br />

industry continue to have strong interactions with<br />

industry, research organizations, <strong>and</strong> scientific peers.<br />

International SEMATECH remains a strong supporter<br />

of our work, pushing forward with next generation<br />

low-k dielectric materials. Building on some previous<br />

work with IBM, we have now partnered with<br />

SEMATECH to extend our investigations of the<br />

fundamentals of the lithographic process. This year,<br />

we completed our work on dielectric metrology for<br />

embedded passive devices <strong>and</strong> initiated two new<br />

projects: one in organic electronics <strong>and</strong> the other<br />

in nanoimprint lithography. Both technologies are<br />

expected to play prominent roles in the future<br />

generations of semiconductor electronics, <strong>and</strong> there<br />

are tremendous scientific <strong>and</strong> technical challenges<br />

to address before that promise is realized.<br />

Following completion of our work on polyolefin<br />

mass spectrometry, we returned to a focus on<br />

quantitative mass spectrometry of polymers. Our<br />

ultimate goal is a st<strong>and</strong>ard method for quantitation of<br />

the absolute molecular mass distribution of polymers,<br />

which would enable researchers to produce their own<br />

reference st<strong>and</strong>ards. This year an interlaboratory<br />

comparison has given us insight into ways to quantify<br />

the accuracy <strong>and</strong> repeatability of matrix-assisted laser<br />

desorption-ionization mass spectrometry (MALDI-MS)<br />

in the identification of multiple end groups that result<br />

from polymer synthesis. Our processing characterization<br />

work continues to break new ground in rheology with<br />

the recent observation of suppression of die swell for<br />

extruded polymers blended with a small quantity of<br />

multiwall carbon nanotubes.<br />

Our biomaterials-related work continues to attract<br />

attention on several fronts, from our collaboration<br />

with the American Dental Association Foundation<br />

on dental restorative materials to our 3-dimensional<br />

structural/functional imaging techniques that<br />

allow for in-situ imaging of cell growth in tissue<br />

engineering scaffolds. To further our underst<strong>and</strong>ing<br />

Executive Summary<br />

of the interface of materials with cell biology,<br />

we are extending our imaging capabilities beyond<br />

structure <strong>and</strong> function to chemistry, through<br />

development of broadb<strong>and</strong> coherent anti-Stokes<br />

Raman scattering (CARS) microscopy. CARS<br />

microscopy holds the potential to enable further<br />

underst<strong>and</strong>ing in regenerative medicine by deciphering<br />

metabolic state <strong>and</strong> cell type in-vitro. Other exciting<br />

advances have been made in methodology for<br />

evaluation of the biocompatibility of materials using<br />

Quantitative Reverse Transcriptase Polymerase<br />

Chain Reaction (QRT-PCR).<br />

Our combinatorial <strong>and</strong> high-throughput researchers<br />

continue to be recognized as pioneers <strong>and</strong> valuable<br />

partners in accelerated materials research, <strong>and</strong> our<br />

<strong>NIST</strong> Combinatorial Methods Center (NCMC)<br />

continues to attract new industrial members.<br />

The latest in the string of innovative approaches<br />

has demonstrated the adaptation of microfluidic (µF)<br />

technology to fabricate polymer molecule libraries<br />

that are compatible with other high-throughput<br />

measurement methods. In addition to this advance<br />

in µF technology, we now have a µF method of<br />

measuring interfacial tension in complex fluids. Our<br />

work on adhesion has progressed with high-throughput<br />

methods to enable rapid quantification of performance<br />

through visualization of debonding mechanisms across<br />

libraries of adhesive conditions.<br />

This year we responded to some specific requests from<br />

other government agencies including a collaboration<br />

with <strong>NIST</strong>’s Office of Law Enforcement St<strong>and</strong>ards<br />

on long-term stability <strong>and</strong> durability of polymeric<br />

materials for ballistic resistant armor (e.g., “bulletproof<br />

vests”). Based on our expertise in composite fibers,<br />

we are developing a minimally invasive technique to<br />

test polymeric fibers from ballistic armor currently in<br />

service. We hope to establish the critical links between<br />

chemical structure, mechanical properties, ballistic<br />

resistance, <strong>and</strong> long-term stability.<br />

As usual, only a portion of our work is included in<br />

this report, so please visit www.nist.gov/polymers<br />

for more details. On our site, you can also download<br />

copies of any of our publications.<br />

As always, I welcome your comments.<br />

Eric J. Amis<br />

Chief, Polymers Division<br />

1

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!