4.6 Article

Generating Singlet Oxygen Bubbles: A New Mechanism for Gas-Liquid Oxidations in Water

Journal

LANGMUIR
Volume 28, Issue 5, Pages 3053-3060

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/la204583v

Keywords

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Funding

  1. National Institute of General Medical Sciences [NIH SC1GM093830]
  2. NYS Empire State Development's Division of Science, Technology & Innovation (NYSTAR)
  3. National Science Foundation [0653056]
  4. Direct For Computer & Info Scie & Enginr
  5. Division Of Computer and Network Systems [0855217] Funding Source: National Science Foundation
  6. Division Of Undergraduate Education
  7. Direct For Education and Human Resources [0653056] Funding Source: National Science Foundation

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Laser-coupled microphotoreactors were developed to bubble singlet oxygen [O-1(2) ((1)Delta(g))] into an aqueous solution containing an oxidizable compound. The reactors consisted of custom-modified SMA fiberoptic receptacles loaded with 150 mu m silicon phthalocyanine glass sensitizer particles, where the particles were isolated from direct contact with water by a membrane adhesively bonded to the bottom of each device. A tube fed O-2 gas to the reactor chambers. In the presence of O-2, singlet oxygen was generated by illuminating the sensitizer particles with 669 nm light from an optical fiber coupled to the top of the reactor. The generated O-1(2) was transported through the membrane by the O-2 stream and formed bubbles in solution. In solution, singlet oxygen reacted with probe compounds (9,10-anthracene dipropionate dianion, trans-2-methyl-2-pentanoate anion, N-benzoyl-D,L-methionine, or N-acetyl-D,L-methionine) to give oxidized products in two stages. The early stage was rapid and showed that O-1(2) transfer occurred via bubbles mainly in the bulk water solution. The later stage was slow; it arose only from O-1(2)-probe molecule contact at the gas/liquid interface. A mechanism is proposed that involves O-1(2) mass transfer and solvation, where smaller bubbles provide better penetration of O-1(2) into the flowing stream due to higher surface-to-volume contact between the probe molecules and O-1(2).

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