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Saving time and energy in the laundry process: Importance of dynamic surface tension, micelle stability and surfactant adsorption.

机译:在洗衣过程中节省时间和能源:动态表面张力,胶束稳定性和表面活性剂吸附的重要性。

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It has been shown that the residual moisture content of fabrics at the end of a centrifugation cycle is related to the equilibrium surface tension of the residual solution in the fabric. However, in the case of lowering the surface tension of solution via increasing concentrations of sodium dodecyl sulfate, a peak is observed in the residual moisture content and the residual moisture of fabrics deviates from the predictions of the LaPlace Equation of capillary rise. This is due to adsorption of surfactant on the fabric and the increase in dynamic surface tension. Several other molecular mechanisms have been found to affect the residual moisture content of fabrics such as the following: dynamic surface tension, micellar stability, chain length compatibility, surfactant-vesicle interactions as well as monolayer penetration. In surfactant systems with stable micelles, the dynamic surface tension of solution is high compared to labile micellar solutions and the resulting residual moisture content of fabrics is higher than the residual moisture of labile micellar systems. Similarly, when the chain lengths of multiple surfactants in a two surfactant system are of the same length, the micellar stability of this system is much higher compared to mismatched chain lengths. The residual moisture content of fabrics in same chain length surfactant systems has been shown to be higher compared to mismatched chains. It has also been established that monolayer penetration can be used to lower the air-liquid surface tension of solution. In this work, we developed a method to lower the air-liquid surface tension values to values much lower than published results (about 7 mN/m). This method was then used to reduce the residual moisture content of fabrics in the laundry process.
机译:已经表明,在离心循环结束时织物的残余水分含量与织物中残余溶液的平衡表面张力有关。然而,在通过增加十二烷基硫酸钠的浓度降低溶液的表面张力的情况下,在残留水分含量中观察到一个峰值,并且织物的残留水分偏离了毛细管上升的拉普拉斯方程的预测。这是由于表面活性剂在织物上的吸附和动态表面张力的增加。已发现其他几种影响织物残留水分的分子机制,例如:动态表面张力,胶束稳定性,链长相容性,表面活性剂与囊泡的相互作用以及单层渗透。在具有稳定胶束的表面活性剂体系中,与不稳定的胶束溶液相比,溶液的动态表面张力高,并且所得的织物残留水分含量高于不稳定的胶束体系的残留水分。类似地,当两种表面活性剂体系中多种表面活性剂的链长相同时,与不匹配的链长相比,该体系的胶束稳定性要高得多。与不匹配的链相比,在相同链长的表面活性剂体系中,织物的残留水分含量更高。还已经确定,单层渗透可用于降低溶液的气液表面张力。在这项工作中,我们开发了一种方法来将气液表面张力值降低到比已公布的结果低得多的值(约7 mN / m)。然后使用该方法减少洗衣过程中织物的残留水分含量。

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