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Convenient characterization of polymers grafted on cellulose nanocrystals via SI-ATRP without chain cleavage
被引:52
|作者:
Zhang, Zhen
[1
,2
]
Tam, Kam C.
[3
]
Sebe, Gilles
[1
,4
]
Wang, Xiaosong
[2
]
机构:
[1] Univ Bordeaux, LCPO, UMR 5629, F-33600 Pessac, France
[2] Univ Waterloo, Waterloo Inst Nanotechnol, Dept Chem, Waterloo, ON N2L 3G1, Canada
[3] Univ Waterloo, Waterloo Inst Nanotechnol, Dept Chem Engn, Waterloo, ON N2L 3G1, Canada
[4] CNRS, LCPO, UMR 5629, F-33600 Pessac, France
基金:
加拿大自然科学与工程研究理事会;
关键词:
Cellulose nanocrystals;
SI-ATRP;
DLS;
DSC;
TGA;
Polystyrene;
TRANSFER RADICAL POLYMERIZATION;
FUNCTIONAL REINFORCING FILLERS;
GLASS-TRANSITION;
POLYSTYRENE;
NANOPARTICLES;
BRUSHES;
BEHAVIOR;
DENSITY;
D O I:
10.1016/j.carbpol.2018.07.060
中图分类号:
O69 [应用化学];
学科分类号:
081704 ;
摘要:
Cleaving is usually required to characterize the molecular weight of grafted polymers on substrates. Here, we report on a technique to estimate the molecular weight of grafted polystyrene (PS) (M-n(grafted) (PS)) in PS-grafted cellulose nanocrystals (PS-g-CNCs) without chain cleavage. PS-g-CNCs were prepared from brominated CNC (CNC-Br) by Surface-Initiated Atom Transfer Radical Polymerization (SI-ATRP) in the presence of sacrificial initiators. Differential scanning calorimetry (DSC), dynamic light scattering (DLS), and thermogravimetric analysis (TGA) of PS-g-CNCs revealed that M-n(grafted) (PS) increased proportionally with monomer conversion. By comparing the mass of grafted PS, deduced from TGA curves, with initiating sites on CNC-Br, M-n(grafted PS) was calculated. The resultant M-n(grafted PS) was the same as M-n of free PS initiated by sacrificial initiators and matched theoretical values calculated according to monomer conversion. Therefore, grafting polymerization from CNC-Br and free polymerization were progressing in a controlled manner with the same propagating rates.
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页码:603 / 609
页数:7
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