Joseph Furgal

Dr. Joseph Furgal

Bowling Green State University, Bowling Green 43403, OH, USA
orcid

Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

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

Representative Publications

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25 November 2021 in Polymer International
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Journal Article
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BRBuddhima Rupasinghe
Buddhima Rupasinghe
Joseph FurgalJoseph Furgal
Joseph Furgal

10 March 2021 in ACS Applied Polymer Materials
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Journal Article
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BRBuddhima Rupasinghe
Buddhima Rupasinghe
Joseph FurgalJoseph Furgal
Joseph Furgal

25 February 2021 in Angewandte Chemie International Edition
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Journal Article
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JGJun Guan
Jun Guan
ZSZejun Sun
Zejun Sun
RARamin Ansari
Ramin Ansari
YLYujia Liu
Yujia Liu
AEAimi Endo
Aimi Endo
RLRichard Laine
Richard Laine

22 October 2019 in Physical Sciences Reviews
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Journal Article
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Joseph FurgalJoseph Furgal
Joseph Furgal
CLChamika U. Lenora
Chamika U. Lenora
The “greening” of silicon chemistry is fundamentally important for the future of the field. Traditional methods used to make silicon-based materials rely on carbon rich processes that are highly energy intensive, cause pollution, and are unsustainable. Researchers have taken up the challenge of developing new chemistries to circumvent the difficulties associated with traditional silicon material synthesis. Most of this work has been in the conversion of the “green” carbon neutral biogenic silica source rice hull ash (RHA, ~85 % silica) into useful silicon building blocks such as silica’s, silicon, and alkoxysilanes by using the inherently higher surface area and reactivity of RHA to sidestep the low reactivity of mined silica sources. This is a review of the work that has been done in the area of developing more environmentally benign methods for the synthesis and use of silicon containing materials to eliminate the negative impact on the environment.

13 August 2020 in ACS Applied Polymer Materials
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Journal Article
Closed access
JGJun Guan
Jun Guan
JAJose Jonathan Rubio Arias
Jose Jonathan Rubio Arias
KTKenji Tomobe
Kenji Tomobe
RARamin Ansari
Ramin Ansari
Maria de Fatima MarquesMaria de Fatima Marques
Maria de Fatima Marques
RLRichard Laine
Richard Laine

16 December 2020 in ACS Omega
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Journal Article
Open access
CLChamika U. Lenora
Chamika U. Lenora
NHNai-Hsuan Hu
Nai-Hsuan Hu
Joseph FurgalJoseph Furgal
Joseph Furgal
A 2,6-bis(2-benzimidazolyl) pyridine-linked silsesquioxane-based semi-branched polymer was synthesized, and its photophysical and metal-sensing properties have been investigated. The polymer is thermally stable up to 285 °C and emits blue in both solid and solution state. The emission of the polymer is sensitive to pH and is gradually decreased and quenched upon protonation of the linkers. The initial emission color is recoverable upon deprotonation with triethylamine. The polymer also shows unique spectroscopic properties in both absorption and emission upon long-term UV irradiation, with red-shifted absorption and emission not present in a simple blended system of phenylsilsesquioxane and linker, suggesting that a long-lived energy transfer or charge separated state is present. In addition, the polymer acts as a fluorescence shift sensor for Zn(II) ions, with red shifts observed from 464 to 528 nm, and reversible binding by the introduction of a competitive ligand such as tetrahydrofuran. The ion sensing mechanism can differentiate Zn(II) from Cd(II) by fluorescence color shifts, which is unique because they are in the same group of the periodic table and possess similar chemical properties. Finally, the polymer system embedded in a paper strip acts as a fluorescent chemosensor for Zn(II) ions in solution, showing its potential as a solid phase ion extractor.