Abstract
Electrospun nanofibers (NFs) incorporated with catalytically active components have gained significant interest in chemical protective clothing. This is because of the desirable properties of the NFs combined with decontamination capability of the active component. Here, a series of metal hydroxide catalysts Ti(OH)x, Zr(OH)4, and Ce(OH)4 were incorporated into three different polymer NF systems. These new polymer/metal hydroxide composite NFs were then evaluated for their catalytic activity against a nerve agent simulant. Two methods were utilized to incorporate the metal hydroxides into the NFs. Method one used direct incorporation of Ti(OH)x, Zr(OH)4, and Ce(OH)4 catalysts, whereas method two employed incorporation of Ti(OH)x via a precursor molecule. Composite NFs prepared via method one resulted in greatly improved reaction rates over the respective pure metal hydroxides due to reduced aggregation of catalysts, with polymer/Ce(OH)4 composite NFs having the fastest reaction rates out of method one materials. Interestingly, composite samples prepared by method two yielded the fastest reaction rates overall. This is because of the homogeneous distribution of the metal hydroxide catalyst throughout the NF. This homogeneous distribution created a hydroxyl-decorated NF surface with a greater number of exposed active sites for catalysis. The hydroxyl-decorated NF surface also resulted in an unexpected highly wettable composite NF, which also was found to contribute to the observed reaction rates. These results are not only promising for applications in chemical protective clothing but also show great potential for application in areas which need highly wettable membrane materials. This includes areas such as separators, antifouling membranes, and certain medical applications.
Original language | English |
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Pages (from-to) | 31378-31385 |
Number of pages | 8 |
Journal | ACS Applied Materials and Interfaces |
Volume | 11 |
Issue number | 34 |
DOIs | |
State | Published - Aug 28 2019 |
Externally published | Yes |
Funding
We acknowledge funding from the Army Research Office (ARO) W911NF1310235 as well as the Joint Science and Technology Office for Chemical Biological Defense (JSTO-CBD) under contract BA13PHM210 at the Edgewood Chemical Biological Center. This experimental work has been carried out with support from the Department of Chemistry at Binghamton University, State University of New York. This work was supported as part of the Multidisciplinary GAANN in Smart Energy Materials, a Graduate Areas of National Need, funded by the U.S. Department of Education, under award #P200A150135. This work was also supported under the NSF REU program award #DMR-1658990. We acknowledge funding from the Army Research Office (ARO) W911NF1310235 as well as the Joint Science and Technology Office for Chemical Biological Defense (JSTO-CBD) under contract BA13PHM210 at the Edgewood Chemical Biological Center. This experimental work has been carried out with support from the Department of Chemistry at Binghamton University, State University of New York. This work was supported as part of the Multidisciplinary GAANN in Smart Energy Materials, a Graduate Areas of National Need, funded by the U.S. Department of Education, under award #P200A150135. This work was also supported under the NSF REU program award #DMR-1658990.
Funders | Funder number |
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Department of Chemistry at Binghamton University | |
JSTO-CBD | BA13PHM210 |
Joint Science and Technology Office for Chemical Biological Defense | |
National Science Foundation | 1658990 |
U.S. Department of Education | 200A150135 |
Army Research Office | W911NF1310235 |
State University of New York | |
Edgewood Chemical Biological Center |
Keywords
- CWAs
- aggregation
- composites
- electrospinning
- metal hydroxide
- nanofibers
- water uptake
- wettability