Plasma Chemistry and Plasma Processing

, Volume 32, Issue 6, pp 1127–1137 | Cite as

Visualization of In Situ Oxidation Process Between Plasma and Liquid Phase in Two Dielectric Barrier Discharge Plasma Reactors Using Planar Laser Induced Fluorescence Technique

  • Xuelan Feng
  • Ting Shao
  • Wentan Wang
  • Binhang Yan
  • Yi ChengEmail author
Original Paper


Cold atmospheric plasma is considered to be a promising approach for decontamination purposes, e.g. dyeing water decoloration. In order to better understand the complex mechanism of the plasma physics coupled with the plasma chemistry involved in the interaction of the polluted water with the discharge plasma, a novel approach was proposed to study the in situ oxidation process between the plasma and liquid phase in two dielectric barrier discharge (DBD) plasma reactors with different bottom shape (concave vs. plane), by using the planar laser induced fluorescence technique to visualize the process dynamics. Rhodamine B was employed as the tracer dye, which was gradually decomposed by the combined effect of the chemically active radicals (OH, O, H2O2, etc.) as well as the intense UV radiation in the DBD plasma process. The results showed that the DBD plasma filaments induced certain fluctuation on the Rhodamine B liquid layer, which accordingly intensified the mass transfer to a large extent thus accelerated the oxidation process. The comparison of the measured concentration fields in the two DBD plasma reactors illustrated that the DBD reactor #1 with concave bottom showed higher oxidation efficiency than the DBD reactor #2 with plane bottom. Additionally, the experiments demonstrated that the oxidation efficiency in the DBD plasma water treatment was much better than that in the reactor with pure oxidation by ozone gas, which can be further improved by injecting the additional oxygen gas bubbles into the liquid phase in the plasma reactor.


Dielectric barrier discharge (DBD) Plasma–liquid interaction Oxidation process Planar laser induced fluorescence (PLIF) Visualization 



Financial supports from National Natural Science Foundation of China (No. 20776074 and No. 21176137) and Specialized Research Fund for the Doctoral Program of Higher Education (No. 20090002110069) are acknowledged. This work is also under the support of Key Lab for Industrial Biocatalysis, Ministry of Education, China.

Supplementary material

Supplementary material 1 (MPG 3,998 kb)

Supplementary material 2 (MPG 4,294 kb)


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Copyright information

© Springer Science+Business Media, LLC 2012

Authors and Affiliations

  • Xuelan Feng
    • 1
  • Ting Shao
    • 1
  • Wentan Wang
    • 1
  • Binhang Yan
    • 1
  • Yi Cheng
    • 1
    Email author
  1. 1.Department of Chemical Engineering, Beijing Key Laboratory of Green Chemical Reaction Engineering and TechnologyTsinghua UniversityBeijingPeople’s Republic of China

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