差示扫描量热法
聚乙二醇
材料科学
增塑剂
艾氏冲击强度试验
混溶性
PEG比率
扫描电子显微镜
傅里叶变换红外光谱
极限抗拉强度
醋酸纤维素
化学工程
高分子化学
纤维素
核化学
复合材料
聚合物
化学
经济
工程类
物理
热力学
财务
作者
Bin Wang,Jinyao Chen,Hanyong Peng,Jing‐Gang Gai,Jian Kang,Ya Cao
标识
DOI:10.1080/00222348.2016.1217185
摘要
Polyethylene glycol (PEG 200) was used as an eco-friendly plasticizer for preparing thermoplastic cellulose acetate (CA) by a twin-screw extruder. The plasticization efficiency of PEG 200 was compared with that of triethyl citrate (TEC). The interaction between polyethylene glycol and CA was investigated by Fourier transform infrared spectroscopy (FT-IR) and differential scanning calorimetry (DSC). Both FT-IR and DSC proved that PEG 200 could form stable and strong hydrogen bonds with CA molecules. Scanning electron microscopy (SEM) revealed that the CA granules were completely disrupted during the extrusion and a continuous and homogeneous phase was observed. The PEG 200-plasticized cellulose acetate (PCA) showed greater viscosity reduction than TEC-plasticized cellulose acetate (TCA) at the same additive levels. Furthermore, the Izod-notched impact strength and elongation at break of PCA were higher than those of TCA. The tensile strength, Izod-notched impact strength and elongation at break of PCA containing 25 wt% PEG 200 reached 31.6 MPa, 20.9 KJ/m2 and 80.5%, respectively, as compared to 39.2 MPa, 10.9 KJ/m2 and 32.3% for 25 wt% TEC plasticized CA.
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