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1.
J Mater Sci Mater Med ; 28(12): 185, 2017 Oct 17.
Article in English | MEDLINE | ID: mdl-29039618

ABSTRACT

We have developed novel photopolymer gels to function as separators in blood collection tubes. By incorporating antioxidants such as α-tocopherol and nitroxides (TEMPO and TEMPOL), the new formulation can be sterilized with electron beam or gamma rays at a dose level of 17 kGy, without inducing premature curing of the photopolymers. For the blood separator gels that contain α-tocopherol, our results show that α-tocopherol plays a decisive role in impeding C-centered free radical propagation reactions through an H-transfer mechanism. This mechanism involves the transfer of an H-atom from the hydroxyl group (OH) of α-tocopherol to the propagating C-centered radical leading to the termination of the polymerization. The sterilization radiation-induced premature curing of the photopolymer was also prevented in the blood separator gel containing nitroxides. For the gels containing TEMPO or TEMPOL, inhibition of the premature curing was achieved through an addition reaction or an H-transfer reaction, respectively. Our results also show that while α-tocopherol is not a contributing factor in the subsequent (time-of-use) UV curing of the gels, nitroxides enhance the UV curing process through nitroxide-mediated living free radical polymerization reactions leading to a decrease in UV curing time. The photopolymer separator gels are shown to function advantageously in clinical laboratory testing, especially for cell-free DNA measurements in blood.


Subject(s)
Gamma Rays , Polymers/chemistry , Sterilization/methods , Ultraviolet Rays , Animals , Antioxidants/chemistry , Cyclic N-Oxides/chemistry , Gels , Materials Testing , Polymers/radiation effects , Spin Labels , X-Rays , alpha-Tocopherol/chemistry
2.
Nat Commun ; 7: 11308, 2016 Apr 14.
Article in English | MEDLINE | ID: mdl-27076111

ABSTRACT

Formic acid is a promising energy carrier for on-demand hydrogen generation. Because the reverse reaction is also feasible, formic acid is a form of stored hydrogen. Here we present a robust, reusable iridium catalyst that enables hydrogen gas release from neat formic acid. This catalysis works under mild conditions in the presence of air, is highly selective and affords millions of turnovers. While many catalysts exist for both formic acid dehydrogenation and carbon dioxide reduction, solutions to date on hydrogen gas release rely on volatile components that reduce the weight content of stored hydrogen and/or introduce fuel cell poisons. These are avoided here. The catalyst utilizes an interesting chemical mechanism, which is described on the basis of kinetic and synthetic experiments.


Subject(s)
Formates/chemistry , Hydrogen/chemistry , Models, Chemical , Carbon Dioxide/chemistry , Catalysis , Hydrogenation , Iridium/chemistry , Kinetics , Magnetic Resonance Spectroscopy , Molecular Structure , Spectrophotometry, Infrared , Water/chemistry
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