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Novel methods to characterize ink - Coating interactions, coating structure and surface energy

机译:表征油墨的新颖方法-涂层相互作用,涂层结构和表面能

摘要

The main focus of this thesis is to analyze capillary adsorption of heterogeneous porous paper coatings. The approach is to develop a novel Gibbs energy model, analyze the structure and surface energy parameters of pilot coated paper and board samples, and compare results to ink tack kinetics. Recent studies have modeled and verified that when inertial force and kinetic energy are included, a smaller diameter capillary starts to fill faster. In addition, other retarding forces, such as local transient sticking of the ink vehicle at surface asperities or chemical inhomogeneities, capillary surface topography and connections between capillaries or physical inhomogeneities in coating, affect the total rate of imbibition. While these resistant factors are very important none of them changes the fact that the basic force driving spontaneous imbibition is the total liquid sorption energy in all various capillaries. This thesis suggests that the change in Gibbs free energy of a liquid associated with its imbibition into capillaries of coating can be used to describe such driving energy. It first derives an expression for this quantity then shows how specific Gibbs energy correlates with the time to reach maximum ink tack, tmax for carbonate-kaolin and latex based coatings. The application of the Gibbs energy model shows that for a relatively constant liquid-solid-vapor interface a larger capillary pore surface area strongly increases the rate of ink setting, as measured by the reduced tmax. In contrast, there is no correlation between ink tack development and pigment surface area or peak pore size of the coating which are currently in use. This new model analyzing Gibbs energy has advantages of combining porous structure variables (volume and diameter, Σ(Vi/Di)) and surface energy parameters (γcosθ) at the interface which often vary concurrently when coating components change, and being independent of many details of time-dependent variables. Surface topography affects liquid-solid-vapor/air interfaces. The second part of the thesis describes simultaneous characterization of surface topographies, using Near-field scanning optical microscopy. Finally, the thesis relates light scattering and absorption to the influence of fine kaolin and carbonates on coating structure and water soluble chemical such as fluorescence whitening agent distribution and efficiency in paper coating.
机译:本文的主要重点是分析非均质多孔纸涂料的毛细管吸附。该方法是建立一个新颖的吉布斯能量模型,分析中试涂布纸和纸板样品的结构和表面能参数,并将结果与​​油墨粘性动力学进行比较。最近的研究已经建模并验证,当包括惯性力和动能​​时,较小直径的毛细管将开始更快地填充。此外,其他阻滞力,例如油墨媒介物在表面凹凸不平处或化学不均匀处的局部瞬态粘附,毛细管表面形貌以及毛细管之间的连接或涂层中的物理不均匀处,也会影响总的吸收速度。尽管这些抗性因子非常重要,但它们都无法改变以下事实:驱动各种自发吸收的基本力是所有各种毛细管中的总液体吸附能。该论文表明,液体的吉布斯自由能的变化与其吸收到涂层的毛细管中有关,可以用来描述这种驱动能。它首先得出该量的表达式,然后显示比吉布斯能量如何与达到最大油墨粘性的时间相关(碳酸盐高岭土和乳胶基涂料的tmax)。吉布斯能量模型的应用表明,对于相对恒定的液-固-蒸气界面,较大的毛细管孔表面积会极大地提高油墨的凝结速率,如通过降低的tmax来衡量。相反,目前正在使用的油墨粘性发展与颜料表面积或涂料的峰值孔径之间没有相关性。这种分析吉布斯能量的新模型的优点是,结合了多孔结构变量(体积和直径,Σ(Vi / Di))和界面处的表面能参数(γcosθ),当涂层组分发生变化时,这些参数通常同时发生变化,并且与许多细节无关时间相关变量的集合。表面形貌影响液体-固体-蒸气/空气界面。论文的第二部分描述了使用近场扫描光学显微镜同时表征表面形貌。最后,本文将光的散射和吸收与精细高岭土和碳酸盐对涂料结构和水溶性化学物质如荧光增白剂的分布和纸张涂料效率的影响联系起来。

著录项

  • 作者

    Ma Deqiang;

  • 作者单位
  • 年度 2009
  • 总页数
  • 原文格式 PDF
  • 正文语种 en
  • 中图分类
  • 入库时间 2022-08-31 15:31:24

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