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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Poly(ethylene oxide) silananted nanosize fumed silica: DSC and TGA characterization of the surface
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Poly(ethylene oxide) silananted nanosize fumed silica: DSC and TGA characterization of the surface

机译:聚环氧乙烷硅烷化的纳米气相二氧化硅:表面的DSC和TGA表征

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Low-molecular-weight poly(ethylene oxide) (PEO) was grafted onto high-surface-area (A380) fumed silica (SiO2) by the use of a silane coupling agent, (CH3O)(3)-Si-(CH2)(3)-(OCH2CH2)(x)-OCH3, with x = 6-9, corresponding to an average molecular weight for the PEO segment of 375 g/mol, PEO(375)-silane. The PEO-grafted silica was characterized by thermogravimetric analysis and differential scanning calorimetry. In the case of PEO(375)-SiO2, the maximum grafting ratio, sigma similar to 2 moleculesm(2) (approximately 33 wt %), corresponded to less coverage than that expected for a monolayer of crystalline upright chains. No crystallization was observed, and the glass transition temperature, T-g, increased from -90 degreesC for the unattached PEO(375)-silane to -54 degreesC for the attached PEO(375)-SiO2 chains. In the case of PEO(5000)-SiO2, a similar maximum weight percent coverage (similar to38%), corresponding to sigma similar to 0.2 moleculesm(2), was obtained. At the highest grafting ratio, the calculated unperturbed chain dimensions in solution were approximately the same as those of the area occupied by the grafted PEO(5000) chains. A melt endotherm, with a melt temperature, T-m, and enthalpy, DeltaH(m), that were decreased with respect to the neat PEO(5000)-silane, but no Tg, was observed. With decreasing sigma, as the surface area occupied by the grafted chains increased with respect to the calculated chain dimensions in solution, DeltaH(m), T-m, and the crystallization temperature, T-c, decreased. The results suggest that the interaction of ethylene oxide segments with surface silanols inhibits the chain mobility necessary for crystallization. [References: 52]
机译:使用硅烷偶联剂(CH3O)(3)-Si-(CH2)将低分子量聚环氧乙烷(PEO)接枝到高表面积(A380)气相法二氧化硅(SiO2)上(3)-(OCH 2 CH 2)(x)-OCH 3,x = 6-9,对应于PEO(375)-硅烷的PEO链段的平均分子量为375g / mol。通过热重分析和差示扫描量热法表征了PEO接枝的二氧化硅。在PEO(375)-SiO2的情况下,最大接枝率sigma类似于2分子/ nm(2)(约33 wt%),对应的覆盖率小于结晶直链单层的预期覆盖率。没有观察到结晶,并且玻璃化转变温度T-g从未连接的PEO(375)-硅烷的-90℃升高到已连接的PEO(375)-SiO 2链的-54℃。在PEO(5000)-SiO2的情况下,获得了相似的最大重量百分比覆盖率(近似38%),对应于类似于0.2分子/ nm(2)的σ。在最高的接枝率下,溶液中计算出的无扰链尺寸与接枝的PEO(5000)链所占面积大致相同。相对于纯PEO(5000)-硅烷,熔融温度为T-m,焓为DeltaH(m)的熔融吸热降低,但未观察到Tg。随着σ的减小,随着相对于计算得出的溶液链尺寸,接枝链占据的表面积增加,DeltaH(m)T-m和结晶温度T-c降低。结果表明环氧乙烷链段与表面硅烷醇的相互作用抑制了结晶所必需的链迁移率。 [参考:52]

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