Jun Xiong

Dr. Jun Xiong

orcid

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

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

Representative Publications

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1 August 2018 in Journal of Hazardous Materials
Verified
Journal Article
Closed access
JXJun Xiong
Jun Xiong
YMYing Ma
Ying Ma
WYWei Yang
Wei Yang
LZLinshan Zhong
Linshan Zhong

1 November 2013 in Journal of Power Sources
Verified
Journal Article
Closed access
JXJun Xiong
Jun Xiong
XDXinfa Dong
Xinfa Dong
YSYibing Song
Yibing Song
Yingchao  DongYingchao Dong
Yingchao Dong

1 August 2021 in Journal of Hazardous Materials
Verified
Journal Article
Closed access
JXJun Xiong
Jun Xiong
LTLei Tian
Lei Tian
RCRuijie Cheng
Ruijie Cheng

1 July 2012 in Journal of Natural Gas Chemistry
Verified
Journal Article
Closed access
JXJun Xiong
Jun Xiong
XDXinfa Dong
Xinfa Dong
LLLingling Li
Lingling Li

1 September 2012 in International Journal of Hydrogen Energy
Verified
Journal Article
Closed access
JXJun Xiong
Jun Xiong
XDXinfa Dong
Xinfa Dong
Yingchao  DongYingchao Dong
Yingchao Dong
XHXufeng Hao
Xufeng Hao
SHStuart Hampshire
Stuart Hampshire

12 January 2019 in Catalysts
Verified
Journal Article
Open access
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JXJun Xiong
Jun Xiong
YMYing Ma
Ying Ma
Catalytic hydrodechlorination (HDC) has been considered as a promising method for the treatment of wastewater containing chlorinated organic pollutants. A continuous flow Pd/carbon nanotube (CNT)-Ni foam micro reactor system was first developed for the rapid and highly efficient HDC with formic acid (FA) as a hydrogen source. This micro reactor system, exhibiting a higher catalytic activity of HDC than the conventional packed bed reactor, reduced the residence time and formic acid consumption significantly. The desired outcomes (dichlorination >99.9%, 4-chlorophenol outlet concentration <0.1 mg/L) can be obtained under a very low FA/substrate molar ratio (5:1) and short reaction cycle (3 min). Field emission scanning electron microcopy (FESEM) and deactivation experiment results indicated that the accumulation of phenol (the main product during the HDC of chlorophenols) on the Pd catalyst surface can be the main factor for the long-term deactivation of the Pd/CNT-Ni foam micro reactor. The catalytic activity deactivation of the micro reactor could be almost completely regenerated by the efficient removal of the absorbed phenol from the Pd catalyst surface.