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Repair of Porous Methylsilsesquioxane Films using Supercritical Carbon Dioxide

机译:超临界二氧化碳修复甲基硅倍半氧烷多孔膜

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摘要

Porous methylsilsesquioxane (p-MSQ) films (JSR LKD 5109) were treated with alkyldimethylmonochlorosilanes having chain lengths of one, four, and eight carbon atoms dissolved in supercritical carbon dioxide at 150-300 atm and 50-60℃ to repair oxygen ashing damage. Fourier transform infrared (FTIR) spectroscopy showed that trimethylchlorosilane (TMCS), butyldimethylchlorosilane (BDMCS), and octyldimethylchlorosilane (ODMCS) reacted with silanol groups on the surfaces of the pores producing covalent Si-O-Si bonds. Self-condensation between alkylsilanols produced a residue on the surface, which was partially removed using a pure scCO_2 rinse. The hydrophobicity of the blanket p-MSQ surface was recovered after silylation treatment as shown by contact angles >85°. The initial dielectric constant of 2.4 ± 0.1 increased to 3.5 ± 0.1 after oxygen plasma ashing and was reduced to 2.6 ± 0.1 by TMCS, 2.8 ± 0.1 by BDMCS, and 3.2 by ODMCS.
机译:用链长分别为1、4和8个碳原子的烷基二甲基单氯硅烷在150-300 atm和50-60℃的超临界二氧化碳中处理多孔甲基硅倍半氧烷(p-MSQ)膜(JSR LKD 5109),以修复氧灰化损伤。傅里叶变换红外(FTIR)光谱表明,三甲基氯硅烷(TMCS),丁基二甲基氯硅烷(BDMCS)和辛基二甲基氯硅烷(ODMCS)与孔表面的硅烷醇基反应生成共价Si-O-Si键。烷基硅烷醇之间的自缩合在表面上产生残留物,使用纯scCO_2漂洗液可以部分除去残留物。甲硅烷基化处理后,覆盖层p-MSQ表面的疏水性得以恢复,如接触角> 85°所示。氧等离子体灰化后,初始介电常数2.4±0.1增至3.5±0.1,TMCS降低至2.6±0.1,BDMCS降低至2.8±0.1,ODMCS降低至3.2。

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