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Viscosity of erythritol and erythritol–water particles as a function of water activity: new results and an intercomparison of techniques for measuring the viscosity of particles

机译:赤藓糖醇和赤藓糖醇-水颗粒的粘度随水分活度的变化:新的结果以及测量颗粒粘度的技术的比较

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A previous study reported an uncertainty of up to 3 orders of magnitude for the viscosity of erythritol (1,2,3,4-butanetetrol)–water particles. To help reduce the uncertainty in the viscosity of these particles, we measured the diffusion coefficient of a large organic dye (rhodamine B isothiocyanate–dextran, average molecular weight ~ 70 000 g mol - 1 ) in an erythritol–water matrix as a function of water activity using rectangular-area fluorescence recovery after photobleaching (rFRAP). The diffusion coefficients were then converted to viscosities of erythritol–water particles using the Stokes–Einstein equation. In addition, we carried out new viscosity measurements of erythritol–water particles using aerosol optical tweezers. Based on the new experimental results and viscosities reported in the literature, we conclude the following: (1)?the viscosity of pure erythritol is 184 - 73 + 122 Pa?s (2 standard deviations); (2)?the addition of a hydroxyl (OH) functional group to a linear Csub4/sub carbon backbone increases the viscosity on average by a factor of 27 - 5 + 6 (2 standard deviations); and (3)?the increase in viscosity from the addition of one OH functional group to a linear Csub4/sub carbon backbone is not a strong function of the number of OH functional groups already present in the molecule up to the addition of three OH functional groups, but the increase in viscosity may be larger when the linear Csub4/sub carbon backbone already contains three OH functional groups. These results should help improve the understanding of the viscosity of secondary organic aerosol particles in the atmosphere. In addition, these results show that at water activity0.4 the rFRAP technique, aerosol optical tweezers technique, and bead-mobility technique give results in reasonable agreement if the uncertainties in the measurements are considered. At water activity0.4 , the mean viscosity values determined by the optical tweezers technique were higher than those determined by the bead-mobility and rFRAP techniques by 1–2 orders of magnitude. Nevertheless, the disagreement in viscosity measured using multiple techniques reported in this paper is smaller than reported previously.
机译:先前的一项研究报道,赤藓糖醇(1,2,3,4-丁丁醇)-水颗粒的粘度不确定性高达3个数量级。为了帮助减少这些颗粒粘度的不确定性,我们测量了一种大型有机染料(罗丹明B异硫氰酸酯-右旋糖酐,平均分子量〜70 000 g mol-1)在赤藓糖醇-水基质中的扩散系数。漂白后矩形区域荧光恢复的水活度(rFRAP)。然后使用Stokes-Einstein方程将扩散系数转换为赤藓糖醇-水颗粒的粘度。此外,我们使用气溶胶光学镊子对赤藓糖醇-水颗粒进行了新的粘度测量。根据新的实验结果和文献报道的粘度,我们得出以下结论:(1)纯赤藓糖醇的粘度为184-73 + 122 Pa?s(2个标准差); (2)在线性C 4 碳主链上加羟基(OH)官能团可使粘度平均提高27-5 + 6(2个标准差); (3)从一个OH官能团加到线性C 4 碳主链上增加的粘度对分子中已经存在的OH官能团的数量没有强烈的影响。虽然添加了三个OH官能团,但是当线性C 4 碳骨架已经包含三个OH官能团时,粘度的增加可能更大。这些结果应有助于增进对大气中次级有机气溶胶颗粒粘度的了解。此外,这些结果表明,如果考虑到测量的不确定性,那么在水分活度> 0.4的情况下,rFRAP技术,气溶胶光镊技术和微珠移动性技术可使结果合理一致。在水分活度<0.4时,通过光镊技术确定的平均粘度值比通过磁珠迁移率和rFRAP技术确定的平均粘度值高1-2个数量级。然而,使用本文报道的多种技术测得的粘度差异比以前报道的要小。

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