热重分析
差示扫描量热法
材料科学
化学工程
聚酯纤维
接触角
分散剂
热分解
乙二醇
扫描电子显微镜
高分子化学
疏水
光泽度(光学)
热分析
复合材料
热机械分析
热稳定性
缩聚物
傅里叶变换红外光谱
润湿
红外光谱学
气相二氧化硅
硬脂酸盐
微晶
作者
Yu‐Tung Hsu,Chiu‐Chun Lai,Ming-Chih Kuo,Pei‐Wen Ruan
摘要
ABSTRACT A series of hydrophobic polyester blends based on poly(ethylene terephthalate) (PET) was prepared via an in situ melt‐blending process during polycondensation, incorporating terephthalic acid (TPA), ethylene glycol (EG), and PDMS of different molecular weights (6000, 60,000, and 100,000 g/mol) via the TPA‐based polycondensation method. Magnesium stearate (SMg) was employed as a dispersant to enhance the hydrophobicity of the resulting modified polyesters. The effects of PDMS molecular weight on the structural, morphological, and thermal properties of the resulting blends were systematically investigated using Fourier‐transform infrared (FTIR) spectroscopy, x‐ray diffraction (XRD), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC). The results revealed that increasing PDMS molecular weight improved the toughness, initial thermal decomposition temperature ( T d5 ), water contact angle, and surface gloss of the PDMS‐modified polyesters, while reducing their crystallinity. The sample containing the highest PDMS molecular weight exhibited the greatest thermal stability, with a decomposition temperature of 396°C. Among all compositions, the M60 PDMS‐modified polyester demonstrated an optimal balance between mechanical strength and thermal stability, indicating its potential for high‐performance hydrophobic material applications.
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