J
Jun Ma
Researcher at Harbin Institute of Technology
Publications - 1523
Citations - 58397
Jun Ma is an academic researcher from Harbin Institute of Technology. The author has contributed to research in topics: Nasopharyngeal carcinoma & Medicine. The author has an hindex of 97, co-authored 1338 publications receiving 39643 citations. Previous affiliations of Jun Ma include Shenyang Aerospace University & University of Technology, Sydney.
Papers
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Enhanced Separation Performance of PVDF/PVP-g-MMT Nanocomposite Ultrafiltration Membrane Based on the NVP-Grafted Polymerization Modification of Montmorillonite (MMT)
TL;DR: The demonstrated method of hydrophobic nanocomposite additive synthesis would be applied for commonly hydroxyl group-containing inorganic nanoparticles, which was favorable to fabricate hydrophilic nanoparticle-enhanced polymer membranes for water treatment.
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Thin-film composite forward osmosis membranes functionalized with graphene oxide–silver nanocomposites for biofouling control
Andreia Fonseca de Faria,Caihong Liu,Caihong Liu,Ming Xie,Ming Xie,François Perreault,François Perreault,Long D. Nghiem,Jun Ma,Menachem Elimelech +9 more
TL;DR: In this paper, the authors proposed the fabrication of anti-biofouling thin-film composite membranes functionalized with graphene oxide-silver nanocomposites in order to prevent bacterial attachment and biofilm growth on membranes.
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Very highly efficient reduction of CO2 to CH4 using metal-free N-doped carbon electrodes
TL;DR: This work reports the first work on the electrocatalytic reduction of CO2 to CH4 using metal-free N-doped carbon electrodes with positive chiral reprograming properties.
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Graphene Platelets and Their Polymer Composites: Fabrication, Structure, Properties, and Applications
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In Situ Surface Chemical Modification of Thin-Film Composite Forward Osmosis Membranes for Enhanced Organic Fouling Resistance
TL;DR: This work presents the first fabrication of an antifouling thin-film composite FO membrane by an in situ technique without postfabrication treatment, and shows a significantly lower flux decline for the in situ modified membranes compared to pristine polyamide.