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Ozonation of Canadian Athabasca asphaltene.

机译:加拿大阿萨巴斯卡沥青质的臭氧化作用。

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Application of ozonation in the petrochemical industry for heavy hydrocarbon upgrading has not been sufficiently explored. Among heavy hydrocarbons, asphaltenes are the heaviest and the most difficult fractions for analysis and treatment. Therefore, ozonation of asphaltenes presents an interesting application in the petrochemical industry.;Commercial application of ozonation in the petrochemical industry has three obstacles: availability of an ozone-resistant and environmentally friendly solvent, the precipitation of ozonation intermediates during reaction, and recovery of the solvent and separation of the ozonation products. Preliminary ozonation of Athabasca oil sands asphaltene in nonparticipating solvents encountered serious precipitation of the ozonation intermediates. The precipitated intermediates could be polymeric ozonides and intermolecular ozonides or polymeric peroxides. Because the inhomogeneous reaction medium caused low ozone efficiency, various participating solvents such as methanol and acetic acid were added to form more soluble hydroperoxides. The mass balance results showed that on average, one asphaltene molecule reacted with 12 ozone molecules through the electrophilic reaction and the subsequent decomposition of ozonation intermediates generated acetone extractable products. GC/MS analysis of these compounds indicated that the free radical reactions could be important for generation of volatile products. The extensively ozonated asphaltene in the presence of participating solvents were refluxed with methanol to generate more volatile products. GC/MS analysis of the methanol-esterified ozonation products indicated that most volatile products were aliphatic carboxylic acid esters generated through cleavage of substituents. Reaction kinetics study showed that asphaltene ozonation was initially a diffusion rate-controlled reaction and later developed to a chemical reaction rate-controlled reaction after depletion of the reactive aromatic sites. Two new solvent systems, a self-sustaining ozonation system and a cyclohexane/acetone/water or a cyclohexane/acetone/methanol system, were studied to overcome the drawback of using halogenated solvents. The self-sustaining ozonation process employed the final ozonation products as the reaction solvent. Compared to the self-sustaining ozonation, the cyclohexane solvent system showed higher ozone efficiency; however, it required dynamic adjustment of the solvent system during ozonation.;An extensively ozonated asphaltene's weight would be doubled. Distillation of the products separated about 45% volatile products having biodiesel-style chemical structures. Compared to distillation, more than 90% of the ozonation products were extractable by acetone. The remaining acetone-insoluble part was further classified by dichloromethane and other solvents of different polarities. The separated ozonation products were good fuel additives or materials for other products.
机译:臭氧化在石化工业中用于重质烃提质的应用尚未得到充分研究。在重质烃中,沥青质是分析和处理中最重,最困难的馏分。因此,沥青质的臭氧化在石油化学工业中呈现出有趣的应用。臭氧化在石油化学工业中的商业应用面临三个障碍:耐臭氧性和环境友好的溶剂的可用性,臭氧化中间体在反应过程中的沉淀以及回收的过程。溶剂和臭氧化产物的分离。 Athabasca油砂沥青质在非参与溶剂中的初步臭氧化过程遇到了臭氧化中间体的严重沉淀。沉淀的中间体可以是聚合的臭氧化物和分子间的臭氧化物或聚合的过氧化物。由于不均匀的反应介质导致臭氧效率低下,因此添加了各种参与溶剂(例如甲醇和乙酸)以形成更易溶的氢过氧化物。质量平衡结果表明,平均而言,一个沥青质分子通过亲电反应与12个臭氧分子反应,随后臭氧化中间体的分解产生了可丙酮提取的产物。这些化合物的GC / MS分析表明,自由基反应对于产生挥发性产物可能很重要。在存在参与溶剂的情况下,将大量臭氧化的沥青质与甲醇回流,以产生更多的挥发性产物。甲醇酯化的臭氧化产物的GC / MS分析表明,大多数挥发性产物是通过取代基的裂解生成的脂肪族羧酸酯。反应动力学研究表明,沥青质臭氧化反应最初是扩散速率控制的反应,后来在反应性芳族位点耗尽后发展为化学反应速率控制的反应。为了克服使用卤化溶剂的缺点,研究了两种新的溶剂系统,即自我维持的臭氧化系统和环己烷/丙酮/水或环己烷/丙酮/甲醇系统。自维持臭氧化过程使用最终的臭氧化产物作为反应溶剂。与自我维持臭氧化相比,环己烷溶剂系统显示出更高的臭氧效率;然而,这需要在臭氧化过程中动态调节溶剂系统。广泛臭氧化的沥青质的重量将增加一倍。产物的蒸馏分离出约45%的具有生物柴油型化学结构的挥发性产物。与蒸馏相比,丙酮可提取90%以上的臭氧化产物。剩余的丙酮不溶部分通过二氯甲烷和其他极性不同的溶剂进一步分类。分离的臭氧化产物是良好的燃料添加剂或用于其他产物的材料。

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