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Trace of the Thermally Induced Evolution Mechanism of Interactions Between Water and Ionic Liquids

机译:水与离子液体相互作用的热诱导演化机理的痕迹

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The thermally induced evolution mechanisms of various interactions in ionic liquids (l-butyl-3-methylimi-dazolium tetrafluoroborate, bmimBF4) and water mixtures have been investigated in this paper. In the near-infrared (NIR) spectroscopy, we focus mainly on v(OH) and v(CH) overtone regions. During heating of bmimBF4 and water mixtures, the v(OH) overtone peak shows a significant blue shift, and the area of this peak shows different changes in three heating regions. By using the perturbation correlation moving window (PCMW) method, we have ascertained the critical temperatures of these three regions: 25-100, 105-160, and 165—190 °C, and we have accordingly performed 2D correlation NIR analysis in three parts. On the basis of 2D study results, we find several types of O-H involved hydrogen bonds (H-B's) in a bmimBF4 and water (15 mol %) mixture and arrive at their evolution mechanisms in each heating region. During heating at 25-100 °C, strong H-B's, such as BF4~-···water···BF4~- and BF4~-···cyclic water dimer···BF4~-, transform into weaker H-B's with simpler structures; at 105-160 °C, the remaining BF4~-···water···BF4~- continues to dissociate, and cation···water H-B's start to dissociate, and a large amount of released free water evaporates; whereas in the final heating region of 165-190 °C, BF4~-···water···BF4~- still exists and continues to dissociate, and in the study of the v(CH) overtone region, we have found that the concentration of water in bmimBF4 affects interactions between cations and anions. In the mixture of bmimBF4 with more water (15 mol %), H-B's between water and bmimBF4 cannot be completely destroyed, even at very high temperature; therefore, only limited new electrostatic interactions would be formed between cations and anions during heating, but in a mixture of bmimBF4 with less water (15 mol %), cations and anions are able to form new electrostatic interactions during the heating process. However, the intensity of these interactions is smaller than that in the 80 °C isothermal process due to the low contacting possibilities among ions at high temperatures.
机译:本文研究了离子液体(1-丁基-3-甲基亚甲基-重氮四氟硼酸盐,bmimBF4)和水混合物中各种相互作用的热诱导演化机理。在近红外(NIR)光谱中,我们主要关注v(OH)和v(CH)泛音区域。在加热bmimBF4和水混合物期间,v(OH)泛音峰显示出明显的蓝移,并且该峰的面积在三个加热区域中显示出不同的变化。通过使用摄动相关移动窗口(PCMW)方法,我们确定了这三个区域的临界温度:25-100、105-160和165-190°C,并相应地在三个部分中进行了二维相关NIR分析。根据2D研究结果,我们发现bmimBF4和水(15 mol%)的混合物中有几种类型的O-H涉及氢键(H-B's),并得出了它们在每个加热区域的演化机理。在25-100°C的加热过程中,强H-B,例如BF4〜-····水···BF4〜-和BF4〜-···循环水二聚体···BF4〜-,转化为较弱的HB具有更简单的结构;在105-160℃下,剩余的BF4〜-···水···BF4〜-继续离解,阳离子···水H-B开始离解,释放出的大量游离水蒸发。而在165-190°C的最终加热区域中,BF4〜-····水···BF4〜-仍然存在并继续离解,在研究v(CH)泛音区域时,我们发现bmimBF4中水的浓度会影响阳离子和阴离子之间的相互作用。在bmimBF4与更多的水(15摩尔%)的混合物中,即使在非常高的温度下,水和bmimBF4之间的H-B也无法完全破坏。因此,在加热过程中,阳离子和阴离子之间只会形成有限的新的静电相互作用,但是在bmimBF4与更少的水(15摩尔%)的混合物中,阳离子和阴离子在加热过程中能够形成新的静电相互作用。但是,由于高温下离子之间的低接触可能性,因此这些相互作用的强度小于80°C等温过程中的相互作用。

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