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首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >Hydrophilization of silicone-urea copolymer surfaces by UV/ozone: Influence of PDMS molecular weight on surface oxidation and hydrophobic recovery
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Hydrophilization of silicone-urea copolymer surfaces by UV/ozone: Influence of PDMS molecular weight on surface oxidation and hydrophobic recovery

机译:UV /臭氧使有机硅-脲共聚物表面亲水化:PDMS分子量对表面氧化和疏水恢复的影响

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摘要

Hydrophilization of polydimethylsiloxane-urea copolymer (PSU) surfaces and the extent of hydrophobic recovery were investigated as a function of; (i) UV/ozone (UV/O) exposure time, (ii) the aging period after UV/O exposure, (iii) sample preparation method, and (iv) polydimethylsiloxane (PDMS) soft segment molecular weight of the copolymer (1500, 3000 and 11,000 g/mol). All copolymers had a constant urea hard segment content of 15% by weight. Samples were prepared by three different methods, which were; solution casting, spin-coating and electrospinning. XPS spectra clearly showed transformation of PDMS into SiO _2 and sub-oxides, which increased gradually with increasing UV/O exposure time. XPS and ATR-FTIR measurements also revealed that the copolymer based on PDMS-11000 displayed the highest amount of SiO_2 formation and overall surface modification. Static water contact angle values of the spincoated silicone-urea copolymer films decreased significantly from 110 to 43 after 3 h of UV/O exposure. Interestingly, the hydrophobicity of the electrospun fibers was retained under similar UV/O exposure conditions, most probably due to the preserved surface roughness. Hydrophobic recovery was evaluated after 2 months of storage at ambient conditions. The slowest recovery was observed for spin-coated copolymer film based on PDMS-11000, due to higher amount of surface oxidation and formation of a thicker SiO_2 barrier layer.
机译:研究了聚二甲基硅氧烷-脲共聚物(PSU)表面的亲水化作用和疏水性回收率的变化。 (i)紫外线/臭氧(UV / O)的暴露时间,(ii)紫外线/ O暴露后的老化时间,(iii)样品制备方法和(iv)共聚物的聚二甲基硅氧烷(PDMS)软链段分子量(1500 ,3000和11,000 g / mol)。所有共聚物的恒定尿素硬链段含量为15重量%。样品是通过三种不同的方法制备的:溶液浇铸,旋涂和静电纺丝。 XPS光谱清楚地表明,PDMS转变为SiO _2和亚氧化物,并随着UV / O暴露时间的增加而逐渐增加。 XPS和ATR-FTIR测量还表明,基于PDMS-11000的共聚物显示出最高的SiO_2形成量和整体表面改性。紫外线/ O暴露3小时后,旋涂有机硅-脲共聚物薄膜的静态水接触角值从110显着降低至43。有趣的是,电纺纤维的疏水性在相似的UV / O暴露条件下得以保留,这很可能是由于保留了表面粗糙度。在环境条件下储存2个月后评估疏水性回收率。对于基于PDMS-11000的旋涂共聚物薄膜,观察到恢复速度最慢,这是由于较高的表面氧化量和较厚的SiO_2阻挡层的形成。

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