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Investigation on Viscoelasticity of Waterborne Polyurethane with Azobenzene-containing Pendant Groups under Ultraviolet and Visible-light Irradiation 被引量:2
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作者 Yi-Jun Liu Dong Liu +2 位作者 Si-Han Li Hua-Qing Liang Fang-Ming Zhu 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2019年第12期1267-1272,I0007,共7页
In this study,a novel waterborne polyurethane(WPU)with azobenzene-containing(azo-containing)pendant groups was synthesized by isophorone diisocyanate,long-chain diol of polycaprolactone,2-ethyl-2-methyl-butanoic acid(... In this study,a novel waterborne polyurethane(WPU)with azobenzene-containing(azo-containing)pendant groups was synthesized by isophorone diisocyanate,long-chain diol of polycaprolactone,2-ethyl-2-methyl-butanoic acid(2,2-dimethylolpropionic acid),10-(4-(phenyldiazenyl)phenoxy)decyl-3-hydroxy-2-(hydroxymethyl)-2-methylpropanoate,and N,N-diethyl-ethanamine(triethylamine).Moreover,the influence of ultraviolet and visible(UV-Vis)light irradiation on the viscoelasticity of azo-containing WPU film in terms of the reversible trans-cis photoisomerization of azo-containing pendant groups was investigated by UV-Vis light spectroscopy,atomic force microscopy,and dynamic thermomechanical analysis.The results revealed that the adhesion of azo-containing WPU with single crystal silicon atomic force microscope probe was about 13 n N when irradiated by 450 nm Vis light for 60 s at 25°C.Subsequently,the adhesion increased to 82 n N after irradiation with 365 nm UV light for 60 s at 25°C.In addition,the azo-containing WPU presented a photo-induced reversible transition of tensile modulus and tanδin the range from about 2 MPa to 22 MPa and 6000 to 0.35 with UV-Vis light cyclic irradiation for 120 s at 25°C,respectively. 展开更多
关键词 WATERBORNE POLYURETHANE VISCOELASTICITY PHOTOISOMERIZATION AZOBENZENE
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Crystallization-driven Self-assembly of Isotactic Polystyrene in N,N-Dimethylformamide
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作者 Qi-hua Zhou Zhi-yun Li +5 位作者 Hua-qing Liang Yong-jiang Long Qing Wu Hai-yang Gao Guo-dong Liang 祝方明 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2015年第4期646-651,共6页
Herein we demonstrate crystallization-driven self-assembly ofisotactic polystyrene (iPS) with high isotacticity and narrow molecular weight distribution and crystallization-induced switching of the morphology of iPS... Herein we demonstrate crystallization-driven self-assembly ofisotactic polystyrene (iPS) with high isotacticity and narrow molecular weight distribution and crystallization-induced switching of the morphology of iPS aggregates in N, N-dimethylformamide (DMF). The formation and morphology switching of the self-assembled aggregates of iPS are investigated by means of dynamic light scattering (DLS), scanning electron microscopy (SEM), differential scanning calorimetry (DSC) and wide angle X-ray diffraction (WXRD). The results reveal that cooling DMF solution of iPS promotes iPS chains to self-assemble into spherical aggregates with a gelled core cross-linked by microcrystals, which is surrounded by solvent-swollen corona. Furthermore, crystallization induces the deformation of iPS aggregates from spherical to plate-like or nest-like. 展开更多
关键词 Isotactic polystyrene N N-Dimethylformamide Crystallization-driven Self-assembly.
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