David Spivak

Dr. David Spivak

orcid

Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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23 September 2007 in Analytical and Bioanalytical Chemistry
Verified
Journal Article
Closed access
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SBSubramanian Balamurugan
Subramanian Balamurugan
AOAnne Obubuafo
Anne Obubuafo
SSSteven A. Soper
Steven A. Soper
David SpivakDavid Spivak
David Spivak

22 January 2014 in Angewandte Chemie International Edition
Verified
Journal Article
Closed access
PDF file
WBWei Bai
Wei Bai
David SpivakDavid Spivak
David Spivak

30 April 2013 in Journal of the American Chemical Society
Verified
Journal Article
Closed access
WBWei Bai
Wei Bai
NGNicholas A. Gariano
Nicholas A. Gariano
David SpivakDavid Spivak
David Spivak

4 February 2009 in Journal of Molecular Recognition
Verified
Journal Article
Closed access
PDF file
AMAndrew C. Meng
Andrew C. Meng
JLJason LeJeune
Jason LeJeune
David SpivakDavid Spivak
David Spivak

24 May 2011 in Langmuir
Verified
Journal Article
Open access
BSBalamurugan Subramanian
Balamurugan Subramanian
NKNamwon Kim
Namwon Kim
WLWonbae Lee
Wonbae Lee
David SpivakDavid Spivak
David Spivak
DNDimitris E. Nikitopoulos
Dimitris E. Nikitopoulos
SSSteven Soper
Steven Soper
Droplet microfluidics performed in poly(methyl methacrylate) (PMMA) microfluidic devices resulted in significant wall wetting by water droplets formed in a liquid–liquid segmented flow when using a hydrophobic carrier fluid such as perfluorotripropylamine (FC-3283). This wall wetting led to water droplets with nonuniform sizes that were often trapped on the wall surfaces, leading to unstable and poorly controlled liquid–liquid segmented flow. To circumvent this problem, we developed a two-step procedure to hydrophobically modify the surfaces of PMMA and other thermoplastic materials commonly used to make microfluidic devices. The surface-modification route involved the introduction of hydroxyl groups by oxygen plasma treatment of the polymer surface followed by a solution-phase reaction with heptadecafluoro-1,1,2,2-tetrahydrodecyl trichlorosilane dissolved in fluorocarbon solvent FC-3283. This procedure was found to be useful for the modification of PMMA and other thermoplastic surfaces, including polycyclic olefin copolymer (COC) and polycarbonate (PC). Angle-resolved X-ray photoelectron spectroscopy indicated that the fluorination of these polymers took place with high surface selectivity. This procedure was used to modify the surface of a PMMA droplet microfluidic device (DMFD) and was shown to be useful in reducing the wetting problem during the generation of aqueous droplets in a perfluorotripropylamine (FC-3283) carrier fluid and could generate stable segmented flows for hours of operation. In the case of PMMA DMFD, oxygen plasma treatment was carried out after the PMMA cover plate was thermally fusion bonded to the PMMA microfluidic chip. Because the appended chemistry to the channel wall created a hydrophobic surface, it will accommodate the use of other carrier fluids that are hydrophobic as well, such as hexadecane or mineral oils.

5 October 2011 in Journal of Molecular Recognition
Verified
Journal Article
Closed access
PDF file
SBSubramanian Balamurugan
Subramanian Balamurugan
David SpivakDavid Spivak
David Spivak