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Surface etching of silicone elastomers by depolymerization

机译:通过解聚作用对有机硅弹性体进行表面蚀刻

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摘要

Silicone elastomer surfaces that are rough at the nanometer to micron scales could be useful for biomaterials, but there are few efficient routes for their preparation. Silicones undergo depolymerization under equilibrating conditions. We demonstrate that surface roughness can be induced by depolymerizing silicone elastomers using triflic acid, tetrabutylammoniumfluoride or KOH as catalysts. The efficiency of depolymerization, however, is decoupled from the roughness that develops. When the catalysts are dissolved in solvents that do not effectively swell silicones, the etching reaction can be mostly directed to the elastomer surface. Acid catalysis leads to slow, nearly homogenous surface erosion with surface roughnesses only increasing from 15 to about 125 nm root mean squared roughness. By contrast, once KOH partitions into the elastomer, the rate of erosion is more efficient than return of the catalyst to the solvent, leading to deep channels and roughnesses of up to ~850 nm. The use of fluoride requires good solvents for silicone, and leads to surfaces of intermediate roughness. Thus, judicious choice of catalyst and solvent permits independent control over depolymerization and the induction of surface roughness.
机译:纳米级至微米级粗糙的有机硅弹性体表面可用于生物材料,但制备它们的有效途径很少。有机硅在平衡条件下进行解聚。我们证明,可以通过使用三氟甲磺酸,氟化四丁基铵或KOH作为催化剂的有机硅弹性体解聚来诱导表面粗糙度。然而,解聚的效率与所产生的粗糙度脱钩。当催化剂溶解在不能有效地使硅酮溶胀的溶剂中时,蚀刻反应大部分可以导向弹性体表面。酸催化导致缓慢,几乎均匀的表面腐蚀,表面粗糙度仅从15 nm到均方根粗糙度增加到约125 nm。相比之下,一旦KOH分配到弹性体中,腐蚀速率比催化剂返回溶剂的效率更高,从而导致较深的通道和高达〜850 nm的粗糙度。氟化物的使用需要良好的有机硅溶剂,并导致中等粗糙度的表面。因此,对催化剂和溶剂的明智选择允许对解聚和表面粗糙度的诱导进行独立控制。

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