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Keywords = fluidic multiplier

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19 pages, 3580 KB  
Article
Ultrafine Aerosol Particle Sizer Based on Piezoresistive Microcantilever Resonators with Integrated Air-Flow Channel
by Maik Bertke, Ina Kirsch, Erik Uhde and Erwin Peiner
Sensors 2021, 21(11), 3731; https://doi.org/10.3390/s21113731 - 27 May 2021
Cited by 10 | Viewed by 4011
Abstract
To monitor airborne nano-sized particles (NPs), a single-chip differential mobility particle sizer (DMPS) based on resonant micro cantilevers in defined micro-fluidic channels (µFCs) is introduced. A size bin of the positive-charged fraction of particles herein is separated from the air stream by aligning [...] Read more.
To monitor airborne nano-sized particles (NPs), a single-chip differential mobility particle sizer (DMPS) based on resonant micro cantilevers in defined micro-fluidic channels (µFCs) is introduced. A size bin of the positive-charged fraction of particles herein is separated from the air stream by aligning their trajectories onto the cantilever under the action of a perpendicular electrostatic field of variable strength. We use previously described µFCs and piezoresistive micro cantilevers (PMCs) of 16 ng mass fabricated using micro electro mechanical system (MEMS) technology, which offer a limit of detection of captured particle mass of 0.26 pg and a minimum detectable particulate mass concentration in air of 0.75 µg/m3. Mobility sizing in 4 bins of a nebulized carbon aerosol NPs is demonstrated based on finite element modelling (FEM) combined with a-priori knowledge of particle charge state. Good agreement of better than 14% of mass concentration is observed in a chamber test for the novel MEMS-DMPS vs. a simultaneously operated standard fast mobility particle sizer (FMPS) as reference instrument. Refreshing of polluted cantilevers is feasible without de-mounting the sensor chip from its package by multiply purging them alternately in acetone steam and clean air. Full article
(This article belongs to the Special Issue Advances in Cantilever Sensors and the Applications)
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14 pages, 3881 KB  
Communication
Development of a Passive Spore Sampler for Capture Enhancement of Airborne Crop Pathogens
by James L. Blackall, Jie Wang, Mostafa R. A. Nabawy, Mark K. Quinn and Bruce D. Grieve
Fluids 2020, 5(2), 97; https://doi.org/10.3390/fluids5020097 - 18 Jun 2020
Cited by 3 | Viewed by 6414
Abstract
Yellow rust spores currently blight commercial and domestic wheat production in areas of East Africa such as Ethiopia. Yellow rust is a hazard to crops which appears asymptomatic for a time, but inevitably causes significant losses in yield once symptoms of infection manifest [...] Read more.
Yellow rust spores currently blight commercial and domestic wheat production in areas of East Africa such as Ethiopia. Yellow rust is a hazard to crops which appears asymptomatic for a time, but inevitably causes significant losses in yield once symptoms of infection manifest themselves to the point where they can be readily observed by the naked eye. Regionally recurrent losses of up to 5% are common and reach as high as 25% in rare cases. Historically, spore sampling has been undertaken by large, cumbersome devices that require heavy power supplies and significant expertise to reliably operate. Moreover, tools for the design and development of such devices are currently limited. This paper, therefore, proposes design and testing processes to develop a spore sampling device that is compact, passive (requires no power to operate), and can better direct spores onto a biomimetic sensor platform enhancing the capture and detection of pathogens. This represents a novel design context for fluidic devices. Performance of the device has been simulated using Lagrangian particle tracking embedded into computational fluid dynamics (CFD) simulations, demonstrating significant improvements across a range of spore Stokes numbers. Experimental validation of numerical simulations was performed using wind tunnel testing and practical performance such as weathervaning was demonstrated. Results show that that the developed sampler is capable of enhancing the probability of yellow rust spores interacting with an internal sensor by a factor of between 20 and 25; demonstrating the effectiveness of the developed design. Full article
(This article belongs to the Special Issue Recent Numerical Advances in Fluid Mechanics, Volume II)
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15 pages, 523 KB  
Article
Rapid, Single-Molecule Assays in Nano/Micro-Fluidic Chips with Arrays of Closely Spaced Parallel Channels Fabricated by Femtosecond Laser Machining
by Brian K. Canfield, Jason K. King, William N. Robinson, William H. Hofmeister and Lloyd M. Davis
Sensors 2014, 14(8), 15400-15414; https://doi.org/10.3390/s140815400 - 20 Aug 2014
Cited by 3 | Viewed by 6799
Abstract
Cost-effective pharmaceutical drug discovery depends on increasing assay throughput while reducing reagent needs. To this end, we are developing an ultrasensitive, fluorescence-based platform that incorporates a nano/micro-fluidic chip with an array of closely spaced channels for parallelized optical readout of single-molecule assays. Here [...] Read more.
Cost-effective pharmaceutical drug discovery depends on increasing assay throughput while reducing reagent needs. To this end, we are developing an ultrasensitive, fluorescence-based platform that incorporates a nano/micro-fluidic chip with an array of closely spaced channels for parallelized optical readout of single-molecule assays. Here we describe the use of direct femtosecond laser machining to fabricate several hundred closely spaced channels on the surfaces of fused silica substrates. The channels are sealed by bonding to a microscope cover slip spin-coated with a thin film of poly(dimethylsiloxane). Single-molecule detection experiments are conducted using a custom-built, wide-field microscope. The array of channels is epi-illuminated by a line-generating red diode laser, resulting in a line focus just a few microns thick across a 500 micron field of view. A dilute aqueous solution of fluorescently labeled biomolecules is loaded into the device and fluorescence is detected with an electron-multiplying CCD camera, allowing acquisition rates up to 7 kHz for each microchannel. Matched digital filtering based on experimental parameters is used to perform an initial, rapid assessment of detected fluorescence. More detailed analysis is obtained through fluorescence correlation spectroscopy. Simulated fluorescence data is shown to agree well with experimental values. Full article
(This article belongs to the Special Issue Opto-Microfluidics for Bio Applications)
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