Ming-Lai Fu

Dr. Ming-Lai Fu

Xiamen Key Laboratory of Municipal and Industrial Solid Waste Utilization and Pollution Control, College of Civil Engineering, Huaqiao University, Xiamen 361020, China

Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

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

Representative Publications

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4 August 2011 in Journal of Soils and Sediments
Verified
Journal Article
Closed access
PDF file
HCHao-Jie Cui
Hao-Jie Cui
MWMing Kuang Wang
Ming Kuang Wang
Ming-Lai FuMing-Lai Fu
Ming-Lai Fu
ECEn Ci
En Ci


1 July 2020 in Applied Catalysis B: Environment and Energy
Verified
Journal Article
Closed access
JYJia-Cheng E. Yang
Jia-Cheng E. Yang
YLYuan Lin
Yuan Lin
HPHui-Hui Peng
Hui-Hui Peng
Baoling YuanBaoling Yuan
Baoling Yuan
Dionysios (Dion) DionysiouDionysios (Dion) Dionysiou
Dionysios (Dion) Dionysiou
Ming-Lai FuMing-Lai Fu
Ming-Lai Fu

12 March 2013 in Journal of Materials Chemistry A
Verified
Journal Article
Closed access
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HCHao-Jie Cui
Hao-Jie Cui
JSJian-Wen Shi
Jian-Wen Shi
BYBaoling Yuan
Baoling Yuan
Ming-Lai FuMing-Lai Fu
Ming-Lai Fu
Two kinds of porous magnetic ferrite nanowires containing manganese (MnFe2O4 and Mn doped Fe3O4) have been successfully synthesized by thermal decomposition of organometallic compounds, using nitrilotriacetic acid (NA) as a chelating agent to coordinate with various ratios of Fe(II) and Mn(II) ions. The resultant MnFe2O4 and Mn doped Fe3O4 nanostructures are superparamagnetic, and have magnetization saturation values of about 45.9 and 48.7 emu g−1 for MnFe2O4 and Mn doped Fe3O4, respectively. The Brunauer–Emmett–Teller specific surface areas of the MnFe2O4 and Mn doped Fe3O4 are 37.8 and 45.4 m2 g−1, respectively. The as-prepared porous MnFe2O4 and Mn doped Fe3O4 nanowires exhibit excellent ability to remove heavy metal ions and organic pollutant in waste water. In addition, these porous magnetic ferrites may be useful in other fields such as biomedicine and Li-ion batteries.

1 March 2019 in Microporous and Mesoporous Materials
Verified
Journal Article
Closed access
JHJiang-Bo Huo
Jiang-Bo Huo
LXLei Xu
Lei Xu
XCXiaoxiao Chen
Xiaoxiao Chen
YZYi Zhang
Yi Zhang
JYJia-Cheng E. Yang
Jia-Cheng E. Yang
Ming-Lai FuMing-Lai Fu
Ming-Lai Fu

11 September 2020 in Journal of Materials Chemistry A
Verified
Journal Article
Closed access
PDF file
XCXiaoxiao Chen
Xiaoxiao Chen
ZWZhiying Wu
Zhiying Wu
DLDengguo Lai
Dengguo Lai
MZMin Zheng
Min Zheng
LXLei Xu
Lei Xu
Ming-Lai FuMing-Lai Fu
Ming-Lai Fu
Solar-driven steam generation is an emerging, attractive, and sustainable technology for potential seawater desalination and wastewater purification. Despite the tremendous progress to date, some technological gaps still remain such as the seemingly unavoidable salt accumulation on the solar absorbers and the generally costly and delicate nanostructures. Here, a cost-effective biomass-derived hydrogel with rationally architected sponge-like skeletons is fabricated through a facile and scalable foaming-polymerization strategy. With advantageous features of organic-polymer chains, inorganic-particles and hierarchical bubble templates, the constructed hydrogel exhibits well-interpenetrative channels and unique porous topography with excellent resilience, fast water-transfer and enhanced light-trapping performances, leading to an ultrahigh and long-term stable evaporation rate of 1.77 ± 0.05 kg m−2 h−1 at 1 sun illumination out of high-salinity seawater (25 wt%) over the entire 7 12 h cycles without deterioration. This promising performance outperforms all the pioneering reported low-cost carbon-based solar absorbers for high-salinity desalination. Importantly, the salt accumulation prefers to crystalize around the edges, spatially isolated from the steam generation surface, achieving complete separation between water and solute. This simple technology to turn “waste” biomass to efficient solar-driven evaporators is anticipated to offer new possibilities to continuously and economically produce pure water from seawater and solute recovery.