Verruto Vincent J, Kilpatrick Peter K
Department of Chemical & Biomolecular Engineering, North Carolina State University, Raleigh, North Carolina 27695, USA.
Langmuir. 2008 Nov 18;24(22):12807-22. doi: 10.1021/la802095m. Epub 2008 Oct 24.
The ever-increasing worldwide demand for energy has led to the upgrading of heavy crude oil and asphaltene-rich feedstocks becoming viable refining options for the petroleum industry. Traditional problems associated with these feedstocks, particularly stable water-in-petroleum emulsions, are drawing increasing attention. Despite considerable research on the interfacial assembly of asphaltenes, resins, and naphthenic acids, much about the resulting interfacial films is not well understood. Here, we describe the use of small-angle neutron scattering (SANS) to elucidate interfacial film properties from model emulsion systems. Modeling the SANS data with both a polydisperse core/shell form factor as well as a thin sheet approximation, we have deduced the film thickness and the asphaltenic composition within the stabilizing interfacial films of water-in-model oil emulsions prepared in toluene, decalin, and 1-methylnaphthalene. Film thicknesses were found to be 100-110 A with little deviation among the three solvents. By contrast, asphaltene composition in the film varied significantly, with decalin leading to the most asphaltene-rich films (30% by volume of the film), while emulsions made in toluene and methylnaphthalene resulted in lower asphaltenic contents (12-15%). Through centrifugation and dilatational rheology, we found that trends of decreasing water resolution (i.e., increasing emulsion stability) and increasing long-time dilatational elasticity corresponded with increasing asphaltene composition in the film. In addition to the asphaltenic composition of the films, here we also deduce the film solvent and water content. Our analyses indicate that 1:1 (O/W) emulsions prepared with 3% (w/w) asphaltenes in toluene and 1 wt % NaCl aqueous solutions at pH 7 and pH 10 resulted in 80-90 A thick films, interfacial areas around 2600-3100 cm (2)/mL, and films that were roughly 25% (v/v) asphaltenic, 60-70% toluene, and 8-12% water. The increased asphaltene and water film composition at pH 10 versus pH 7, along with unique dynamic interfacial tension profiles, suggested that the protonation state of carboxylic moieties within asphaltenes impacts the final film properties. This was further supported when we characterized similar asphaltenic emulsions that also contained 9-anthracence carboxylic acid (ACA). Addition of this aromatic acid led to slightly thinner films (70-80 A) that were characteristically more aqueous (up to 20% by volume) and 5-6% (v/v) ACA. This unique in situ characterization (deduced entirely from SANS data from emulsion samples) of the entire film composition calls for further investigation regarding the role this film-based water plays in emulsion stability.
全球对能源的需求不断增长,促使重质原油升级,富含沥青质的原料成为石油行业可行的炼油选择。与这些原料相关的传统问题,尤其是稳定的石油包水乳液,正受到越来越多的关注。尽管对沥青质、树脂和环烷酸的界面组装进行了大量研究,但对由此形成的界面膜仍有许多不甚了解之处。在此,我们描述了使用小角中子散射(SANS)来阐明模型乳液体系的界面膜性质。通过用多分散核/壳形状因子以及薄片近似对SANS数据进行建模,我们推导出了在甲苯、十氢化萘和1-甲基萘中制备的模型油包水乳液稳定界面膜的膜厚度和沥青质组成。发现膜厚度为100 - 110 Å,三种溶剂之间偏差很小。相比之下,膜中的沥青质组成变化显著,十氢化萘导致形成的膜中沥青质含量最高(占膜体积的30%),而在甲苯和甲基萘中制备的乳液沥青质含量较低(12 - 15%)。通过离心和拉伸流变学,我们发现水分辨率降低(即乳液稳定性增加)和长时间拉伸弹性增加的趋势与膜中沥青质组成增加相对应。除了膜的沥青质组成外,我们还推导出了膜的溶剂和水含量。我们的分析表明,在pH值为7和pH值为10的条件下,用3%(w/w)沥青质在甲苯中与1 wt% NaCl水溶液制备的1:1(油/水)乳液,形成的膜厚度为80 - 90 Å,界面面积约为2600 - 3100 cm²/mL,膜中沥青质约占25%(v/v),甲苯占60 - 70%,水占8 - 12%。与pH值为7相比,pH值为10时膜中沥青质和水的组成增加,以及独特的动态界面张力曲线,表明沥青质中羧基部分的质子化状态会影响最终的膜性质。当我们对也含有9-蒽羧酸(ACA)的类似沥青质乳液进行表征时,进一步证实了这一点。添加这种芳香酸导致膜稍微变薄(70 - 80 Å),其特征是含水量更高(高达20%体积)且含有5 - 6%(v/v)的ACA。这种对整个膜组成的独特原位表征(完全从乳液样品的SANS数据推导得出),需要进一步研究这种基于膜的水在乳液稳定性中所起的作用。