首页> 外文OA文献 >Molecule-surface recognition between heterocyclic aromatic compounds and kaolinite in toluene investigated by molecular theory of solvation and thermodynamic and kinetic experiments
【2h】

Molecule-surface recognition between heterocyclic aromatic compounds and kaolinite in toluene investigated by molecular theory of solvation and thermodynamic and kinetic experiments

机译:用溶剂化分子理论和热力学及动力学实验研究甲苯中杂环芳族化合物与高岭石之间的分子表面识别

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Molecular recognition interactions between kaolinite and a series of heterocyclic aromatic compounds (HAC) representative of the N- and S-containing moieties in petroleum asphaltene macromolecules are investigated using the three-dimensional reference interaction site model with the Kovalenko-Hirata closure approximation (3D-RISM-KH) theory of solvation and experimental techniques in toluene solvent. The statistical-mechanical 3D-RISM-KH molecular theory of solvation predicts the adsorption configuration and thermodynamics from the 3D site density distribution functions and total solvation free energy, respectively, for adsorption of HAC and toluene on kaolinite. Spectrophotometric measurements show that, among the HAC studied, only acridine and phenanthridine adsorb quantitatively on kaolinite. For these pyridinic HAC, the adsorption results fitted to the Langmuir isotherm in the monolayer domain suggest a uniform monolayer of HAC molecules. The 3D-RISM-KH studies predict that the aluminum hydroxide surface of kaolinite is preferred for HAC adsorption due to strong hydrogen bonding with the pyridinic N atoms, while the rest of the HAC adsorb weaker. Adsorption on the silicon oxide side is weak and delocalized, as evident from the 3D solvation free energy density. Toluene sites effectively compete with non-hydrogen bonding HAC, such as fused thiophenes, for the kaolinite surface. The adsorption enthalpy and phenanthridine-acridine loading ratio are calculated and correlated with the experimentally determined Langmuir constant and adsorption loading. This combined experimental and computational modeling approach is aimed to provide insight into the specific interactions among clays, bitumen, and solvents so as to help accelerate the development of environmentally friendly and efficient desorption systems for nonaqueous extraction of bitumen from Oil Sands, an important unconventional petroleum reserve.
机译:使用三维参考相互作用位点模型和Kovalenko-Hirata闭合逼近(3D-),研究了高岭石与一系列代表石油沥青质大分子中N和S的杂环芳族化合物(HAC)之间的分子识别相互作用RISM-KH)在甲苯溶剂中的溶剂化理论和实验技术。统计力学的3D-RISM-KH溶剂化分子理论分别根据3D位置密度分布函数和总溶剂化自由能预测HAC和甲苯在高岭石上的吸附构型和热力学。分光光度法测量表明,在所研究的HAC中,只有a啶和菲啶定量吸附在高岭石上。对于这些吡啶二酮HAC,拟合到Langmuir等温线在单层结构域中的吸附结果表明HAC分子是均匀的单层。 3D-RISM-KH研究预测高岭石的氢氧化铝表面更适合HAC吸附,因为它与吡啶N原子牢固地形成氢键,而其余HAC吸附较弱。从3D溶剂化自由能密度可以明显看出,氧化硅一侧的吸附很弱且分散。甲苯位点可与非氢键HAC(例如稠合噻吩)有效竞争高岭石表面。计算吸附焓和菲啶-啶负载比,并将其与实验确定的朗缪尔常数和吸附负载相关联。这种结合了实验和计算模型的方法旨在深入了解粘土,沥青和溶剂之间的特定相互作用,从而有助于加快开发环境友好且高效的解吸系统,以从油砂(一种重要的非常规石油)中非水提炼沥青。保留。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号