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Integration of microscale fluidic elements,
whether for incorporating several elements
to make a device or for massively parallelizing
a microfluidic analysis, is essential for reaching
microfluidics' potential for better, faster,
and cheaper chemical/biochemical analysis.
Complex fluid flow control at microscales requires
microvalves. Many microfabricated valves have
been proposed; however, few can hold off pressures
more than a few bars. High-pressure liquid
chromatography typically uses pressures above
200 bar, requiring that fluid routing devices
be designed for high pressures.
Mobile polymer monolith are in use at Sandia
for a variety of fluid control elements. These
polymer monoliths are closed-shell, porous
polymer structures; a typical modulus of elasticity
is .01-.1 GN/m2. The mobile monoliths
are used in conjunction with multiple-level
etched silica microchannels for fluid control.
An example is shown at right, in which a check
valve is constructed by constructing a mobile
polymer piston within a contained space. This
piston moves in response to pressure differences >1
psi. When pressure is applied at left, the
piston moves to the right but allows flow
to proceed along the bypass. Thus flow can
move from left to right. When pressure is
applied at right, the piston moves to the
left and seals at the interface between the
deeply etched channel (60 um) and the shallowly-etched
channel (20 um) to which it is connected.
We laser-fabricate these microvalves by photoinitiating
phase-separated polymer monoliths in-situ. The
microchannel and the lithographic mask define
the shape the monolith takes upon polymerization.
Monomers, solvents, and polymerization time
define the bulk properties of the monolith.
In capillary, these elements, have been shown
to seal against 340 bar with leak rates below
50 pl/min. On chip; pressures over 200 bar
have been sealed, with worst-case leak rates
on the order of 1 nl/min. Pressure required
to actuate these mobile elements is shown at
right, where the pressure has been normalized
to a nominally 100 micron diameter microchannel.
At low crosslinking levels, the pressure required
to actuate these elements can be under 1 psi.
Upcoming Presentations |
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B.J. Kirby, T.J. Shepodd, D.S. Reichmuth
"Metered Microchip Pressure Injections Using Mobile
Polymer Monolith Microvalves, " oral presentation,
HPCE 2003,
January 2003, San Diego, CA. |
References |

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B.J. Kirby, T.J. Shepodd
"Microvalve architectures for high-pressure hydraulic
and electrokinetic fluid control in microchips," in Micro
Total Analysis Systems 2002, Kluwer Academic Publishers,
p. 338, 2002. |
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B.J. Kirby, T.J. Shepodd, E.F. Hasselbrink
"Voltage-Addressable on/off microvalves for high-pressure
microchip separations," J. Chrom. A , v. 979,
p. 147-154, 2002. |
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E.F. Hasselbrink, T.J. Shepodd, J.E.
Rehm
"High Pressure Microfluidic Control in Lab-on-a-Chip
Devices using Mobile Polymer Monoliths," Analytical
Chemistry , v74, p4913-4918, 2002. |

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J.E. Rehm, T.J. Shepodd, E.F. Hasselbrink
"Mobile Flow Control Elements For High-Pressure Micro-Analytical
Systems Fabricated Using In-Situ Polymerization," in Micro
Total Analysis Systems 2001, Kluwer Academic Publishers,
2001. |
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