Mujie Yang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
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Research Interests
Mujie Yang has a total of 38 co-authors. Here are the top co-authors by number of shared publications:
Yang Li
Department of Polymer Science and Engineering, Zhejiang University, Hangzhou, 310027 P.R. China; fax: +86-571-87952444
9 shared publicationsDan Luo
Key Laboratory of Macromolecular Synthesis and Functionalization, Ministry of Education, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou 310027, China
4 shared publicationsJichang Feng
MOE Key Laboratory of Macromolecular Synthesis and Functionalization, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou 310027, China
4 shared publications- Yang Li
MOE Key Laboratory of Macromolecular Synthesis and Functionalization, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou 310058, China
4 shared publications Kuan Liu
Department of Polymer Science and Engineering, Zhejiang University, Hangzhou, 310027 P.R. China; fax: +86-571-87952444
3 shared publicationsXin Lv
Department of Polymer Science and Engineering, Zhejiang University, Hangzhou 310027, China Key Laboratory of Macromolecule Synthesis and Functionalization (Zhejiang University), Ministry of Education, Hangzhou 310027, People's Republic of China
3 shared publications
Latest Publications
- 1 December 2019
- Published by Elsevier in Journal of Colloid and Interface Science
- Vol. 557, 709-721
3D MoS2@TiO2@poly(methyl methacrylate) nanocomposite with enhanced photocatalytic activity
- 1 December 2019
- Published by Elsevier in Journal of Colloid and Interface Science
- Vol. 557, 709-721
3D MoS2@TiO2@poly(methyl methacrylate) nanocomposite with enhanced photocatalytic activity
- 1 December 2017
- Published by Elsevier in Journal of Colloid and Interface Science
- Vol. 508, 500-507
TiO2 nanoparticles supported on PMMA nanofibers for photocatalytic degradation of methyl orange
- 1 December 2017
- Published by Elsevier in Journal of Colloid and Interface Science
- Vol. 508, 500-507
TiO2 nanoparticles supported on PMMA nanofibers for photocatalytic degradation of methyl orange
- 17 February 2011
- Published by Wiley in Journal of Applied Polymer Science
- Vol. 121 (1) , 217-225
Hyperbranched polymer based on triphenylamine and pyridine: Fluorescent chemosensors for palladium ions
- 17 February 2011
- Published by Wiley in Journal of Applied Polymer Science
- Vol. 121 (1) , 217-225
Hyperbranched polymer based on triphenylamine and pyridine: Fluorescent chemosensors for palladium ions
- 12 January 2011
- Published by Wiley in Journal of Applied Polymer Science
- Vol. 120 (5) , 2979-2984
Preparation and characterization of novel crosslinked poly[glycidyl methacrylate–poly(ethylene glycol) methyl ether methacrylate] as gel polymer electrolytes
In this study, glycidyl methacrylate was copolymerized with poly(ethylene glycol) methyl ether methacrylate to obtain a copolymer {poly[glycidyl methacrylate–poly(ethylene glycol) methyl ether methacrylate] [P(GMA–PEGMA)]}, which was crosslinked with α,ω‐diamino poly(propylene oxide) (Jeffamine) at various weight ratios and molecular weights to form novel gel polymer electrolytes (GPEs). The crosslinked copolymers were characterized by Fourier transform infrared spectroscopy and thermal analysis. The crosslinked polymers were amorphous in the pristine state and became crystallized after they were doped with lithium electrolyte. Furthermore, the crosslinking degree of the crosslinked polymers increased with increasing weight ratio of Jeffamine, and both the swelling properties and mechanical behaviors of the crosslinked polymers were heavily affected by the weight ratio and molecular weight of Jeffamine. The ionic conductivity (σ) of the GPEs from the crosslinked copolymers was determined by alternating‐current impedance spectroscopy. A higher molecular weight and increased weight ratio of Jeffamine resulted in a higher σ. The GPE based on P(GMA–PEGMA) crosslinked with an equal weight of Jeffamine D2000 exhibited the highest σ of 8.29 × 10−4 S/cm at 25°C and had a moderate mechanical strength. These crosslinked copolymers could be potential candidates for the construction of rechargeable lithium batteries. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011
- 12 January 2011
- Published by Wiley in Journal of Applied Polymer Science
- Vol. 120 (5) , 2979-2984
Preparation and characterization of novel crosslinked poly[glycidyl methacrylate–poly(ethylene glycol) methyl ether methacrylate] as gel polymer electrolytes
In this study, glycidyl methacrylate was copolymerized with poly(ethylene glycol) methyl ether methacrylate to obtain a copolymer {poly[glycidyl methacrylate–poly(ethylene glycol) methyl ether methacrylate] [P(GMA–PEGMA)]}, which was crosslinked with α,ω‐diamino poly(propylene oxide) (Jeffamine) at various weight ratios and molecular weights to form novel gel polymer electrolytes (GPEs). The crosslinked copolymers were characterized by Fourier transform infrared spectroscopy and thermal analysis. The crosslinked polymers were amorphous in the pristine state and became crystallized after they were doped with lithium electrolyte. Furthermore, the crosslinking degree of the crosslinked polymers increased with increasing weight ratio of Jeffamine, and both the swelling properties and mechanical behaviors of the crosslinked polymers were heavily affected by the weight ratio and molecular weight of Jeffamine. The ionic conductivity (σ) of the GPEs from the crosslinked copolymers was determined by alternating‐current impedance spectroscopy. A higher molecular weight and increased weight ratio of Jeffamine resulted in a higher σ. The GPE based on P(GMA–PEGMA) crosslinked with an equal weight of Jeffamine D2000 exhibited the highest σ of 8.29 × 10−4 S/cm at 25°C and had a moderate mechanical strength. These crosslinked copolymers could be potential candidates for the construction of rechargeable lithium batteries. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011
- 3 August 2010
- Published by Wiley in Journal of Applied Polymer Science
- Vol. 118 (3) , 1527-1533
Novel amphiphilic polymer gel electrolytes based on (PEG‐b‐GMA)‐co‐MMA
- 3 August 2010
- Published by Wiley in Journal of Applied Polymer Science
- Vol. 118 (3) , 1527-1533
Novel amphiphilic polymer gel electrolytes based on (PEG‐b‐GMA)‐co‐MMA
- Open Access
- 1 December 2009
- Published by Walter de Gruyter GmbH in e-Polymers
- Vol. 9 (1) , 868-872
Novel electron-acceptor conjugated polymer materials based on poly(thienylene ethynylene) derivatives
Novel electron-acceptor materials based on poly(thienylene ethynylene) derivatives (PTE-BT and PTE-DCNTB) were synthesized and characterized by FTIR spectroscopy. Their thermal, electrochemical and optical properties were investigated. The π-conjugated polymers are soluble in common organic solvents. The maximum UV-Vis absorptions of PTE-BT and PTE-DCNTB in solution are observed at 460 and 390 nm, respectively. The electrochemical band gap was found to be 1.89 eV for PTE-BT and 2.01 eV for PTE-DCNTB. Both polymers are promising as electron-acceptor materials for photovoltaic applications.
- 1 December 2009
- Published by Walter de Gruyter GmbH in e-Polymers
- Vol. 9 (1) , 868-872
Open AccessNovel electron-acceptor conjugated polymer materials based on poly(thienylene ethynylene) derivatives
Novel electron-acceptor materials based on poly(thienylene ethynylene) derivatives (PTE-BT and PTE-DCNTB) were synthesized and characterized by FTIR spectroscopy. Their thermal, electrochemical and optical properties were investigated. The π-conjugated polymers are soluble in common organic solvents. The maximum UV-Vis absorptions of PTE-BT and PTE-DCNTB in solution are observed at 460 and 390 nm, respectively. The electrochemical band gap was found to be 1.89 eV for PTE-BT and 2.01 eV for PTE-DCNTB. Both polymers are promising as electron-acceptor materials for photovoltaic applications.
- 16 July 2009
- Published by Wiley in Journal of Applied Polymer Science
- Vol. 114 (5) , 2755-2763
In situ compatibilization between polystyrene‐grafted nano‐sized TiO2 and polypropylene with Friedel‐Crafts catalyst
The application of Friedel‐Crafts (FC) alkylation reaction to the in situ compatibilization between polystyrene‐grafted nano‐sized TiO2 (PS‐grafted TiO2) and polypropylene (PP) was assessed. The PS‐grafted TiO2 was first prepared via dispersion polymerization of styrene (St) using 3‐(trimethoxysilyl) propyl methacrylate treated nano‐sized TiO2 (MPS‐treated TiO2) as cores, and then dispersed within PP by melt blending with different contents of FC catalyst, AlCl3/St, to give PP/PS‐grafted TiO2 nanocomposites. The dispersion of PS‐grafted TiO2 in PP and interfacial adhesion of PP/PS‐grafted TiO2 nanocomposites were characterized by transmission electron microscopy (TEM) and scanning electron microscopy (SEM), respectively. The results indicated that the dispersion of PS‐grafted TiO2 in PP could be improved, with an enhancement of interfacial adhesion between TiO2 and PP, by introducing FC catalyst with adequate concentration, which led to a better thermal stability and resistance to ultraviolet (UV) aging of PP/PS‐grafted TiO2 nanocomposites. The effect of FC catalyst on the compatibilization between the PS‐grafted TiO2 and PP was discussed based on FC alkylation reaction mechanism. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009
- 16 July 2009
- Published by Wiley in Journal of Applied Polymer Science
- Vol. 114 (5) , 2755-2763
In situ compatibilization between polystyrene‐grafted nano‐sized TiO2 and polypropylene with Friedel‐Crafts catalyst
The application of Friedel‐Crafts (FC) alkylation reaction to the in situ compatibilization between polystyrene‐grafted nano‐sized TiO2 (PS‐grafted TiO2) and polypropylene (PP) was assessed. The PS‐grafted TiO2 was first prepared via dispersion polymerization of styrene (St) using 3‐(trimethoxysilyl) propyl methacrylate treated nano‐sized TiO2 (MPS‐treated TiO2) as cores, and then dispersed within PP by melt blending with different contents of FC catalyst, AlCl3/St, to give PP/PS‐grafted TiO2 nanocomposites. The dispersion of PS‐grafted TiO2 in PP and interfacial adhesion of PP/PS‐grafted TiO2 nanocomposites were characterized by transmission electron microscopy (TEM) and scanning electron microscopy (SEM), respectively. The results indicated that the dispersion of PS‐grafted TiO2 in PP could be improved, with an enhancement of interfacial adhesion between TiO2 and PP, by introducing FC catalyst with adequate concentration, which led to a better thermal stability and resistance to ultraviolet (UV) aging of PP/PS‐grafted TiO2 nanocomposites. The effect of FC catalyst on the compatibilization between the PS‐grafted TiO2 and PP was discussed based on FC alkylation reaction mechanism. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009
- 30 January 2009
- Published by Wiley in Journal of Applied Polymer Science
- Vol. 112 (3) , 1287-1293
Synthesis and humidity sensitive properties of pyrrole‐based polyelectrolytes
- 30 January 2009
- Published by Wiley in Journal of Applied Polymer Science
- Vol. 112 (3) , 1287-1293
Synthesis and humidity sensitive properties of pyrrole‐based polyelectrolytes
- 21 January 2009
- Published by Wiley in Polymers for Advanced Technologies
- Vol. 20 (6) , 514-518
A novel calixarene‐containing hyperbranched aliphatic polyester incorporated with pendant europium complexes
A novel calixarene‐containing hyperbranched aliphatic polyester incorporated with pendant europium complexes (H20‐Cal‐Eu) was synthesized and characterized by FTIR, UV, and element analysis. The polymer H20‐Cal‐Eu shows a glass‐transition temperature (Tg) of 127°C, and a deposition temperature in the range of 280–600°C, as revealed by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA), respectively. The investigation on its photoluminescence (PL) properties revealed that the polymer emitted a remarkably strong red luminescence. Furthermore, its half spectral bandwidth of the polymer film is only about 10 nm as determined from luminescence spectra, suggesting that the light is nearly monochromatic. It is proposed that the hyperbranched polymer (HBP) containing rare earth element exhibits great potential as a red light emitting material. Copyright © 2009 John Wiley & Sons, Ltd.
- 21 January 2009
- Published by Wiley in Polymers for Advanced Technologies
- Vol. 20 (6) , 514-518
A novel calixarene‐containing hyperbranched aliphatic polyester incorporated with pendant europium complexes
A novel calixarene‐containing hyperbranched aliphatic polyester incorporated with pendant europium complexes (H20‐Cal‐Eu) was synthesized and characterized by FTIR, UV, and element analysis. The polymer H20‐Cal‐Eu shows a glass‐transition temperature (Tg) of 127°C, and a deposition temperature in the range of 280–600°C, as revealed by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA), respectively. The investigation on its photoluminescence (PL) properties revealed that the polymer emitted a remarkably strong red luminescence. Furthermore, its half spectral bandwidth of the polymer film is only about 10 nm as determined from luminescence spectra, suggesting that the light is nearly monochromatic. It is proposed that the hyperbranched polymer (HBP) containing rare earth element exhibits great potential as a red light emitting material. Copyright © 2009 John Wiley & Sons, Ltd.
- 21 January 2009
- Published by Wiley in Polymers for Advanced Technologies
- Vol. 20 (6) , 509-513
Humidity sensitive properties of copolymer of quaternary ammonium salt with polyether–salt complex
- 21 January 2009
- Published by Wiley in Polymers for Advanced Technologies
- Vol. 20 (6) , 509-513
Humidity sensitive properties of copolymer of quaternary ammonium salt with polyether–salt complex