[1] Healy W. C., Jr C. W. M., Peterson R. T. A new approach to blending octane[J]. Proc Am Inst, 1959, 39(3):132-136 [2] Ghosh P., Hickey K. J., Jaffe S. B. Development of a Detailed Gasoline Composition-Based Octane Model[J]. Industrial & Engineering Chemistry Research, 2006, 45(1):337-345 [3] Teng S. T., Williams A. D., Urdal K. Detailed Hydrocarbon Analysis of Gasoline by GC-MS (SI-PIONA)[J]. Journal of high resolution chromatography, 1994, (17) [4] White C. M., Hackett J., Anderson R. R., et al. Linear temperature programmed retention indices of gasoline range hydrocarbons and chlorinated hydrocarbons on cross‐linked polydimethylsiloxane[J]. Journal of High Resolution Chromatography, 1992, 15(2):105-120 [5] Cui C., Billa T., Zhang L., et al. Molecular Representation of the Petroleum Gasoline Fraction[J]. Energy & Fuels, 2018, 32(2):1525-1533 [6] Knocking Characteristics of Pure Hydrocarbons. Special Technical Publication No. 225[S]. West Conshohocken, PA: American Society for Testing Materials, 1958 [7] API Technical Data Book on Petroleum Refining[M]. Washington, DC: American Petroleum Institute, 1982 [8] LOVELL W. G. Knocking Characteristics of Hydrocarbons[J]. Industrial and Engineering Chemistry, 1948, 40(12):2388-2438 [9] Katritzky A. R., Lobanov V. S., Karelson M. QSPR: the correlation and quantitative prediction of chemical and physical properties from structure[J]. Chemical Society Reviews, 1995, 24[10] Joback K. G., Reid R. C. Estimation of Pure-component Properties From Group-contributions[J]. Chemical Engineering Communications, 1987, 57(1-6):233-243[11] Albahri T. A. Structural Group Contribution Method for Predicting the Octane Number of Pure Hydrocarbon Liquids[J]. Industrial & Engineering Chemistry Research, 2003, 42(3):657-662[12] Kubic W. L., Jenkins R. W., Moore C. M., et al. Artificial Neural Network Based Group Contribution Method for Estimating Cetane and Octane Numbers of Hydrocarbons and Oxygenated Organic Compounds[J]. Industrial & Engineering Chemistry Research, 2017, 56(42):12236-12245[13] Wiener H. Structural determination of paraffin boiling points[J]. Journal of the American Chemical Society, 1947, 69(1):17-20[14] Gani R., Harper P. M., Hostrup M. Automatic Creation of Missing Groups through Connectivity Index for Pure-Component Property Prediction[J]. Industrial & Engineering Chemistry Research, 2005, 44(18):7262-7269[15] Kier L. B., Hall L. H. Molecular connectivity in structure-activity analysis[M]. Research Studies, 1986[16] Hukkerikar A. S., Meier R. J., Sin G., et al. A method to estimate the enthalpy of formation of organic compounds with chemical accuracy[J]. Fluid Phase Equilibria, 2013, 348:23-32[17] Hukkerikar A. S., Sarup B., Ten Kate A., et al. Group-contribution+ (GC+) based estimation of properties of pure components: Improved property estimation and uncertainty analysis[J]. Fluid Phase Equilibria, 2012, 321:25-43[18] Smolenskii E. A., Ryzhov A. N., Bavykin V. M., et al. Octane numbers (ONs) of hydrocarbons: a QSPR study using optimal topological indices for the topological equivalents of the ONs[J]. Russian Chemical Bulletin, 2007, 56(9):1681-1693[19] Ryzhov A. N., Strizhakova Y. A., Smolenskii E. A., et al. Modeling the octane numbers of alkenes by the inverse function method[J]. Petroleum Chemistry, 2011, 51(5):354-362[20] Duvenaud D., Maclaurin D., Aguilera-Iparraguirre J., et al. Convolutional Networks on Graphs for Learning Molecular Fingerprints[J]. 2015, [21] Xu Y., Pei J., Lai L. Deep Learning Based Regression and Multiclass Models for Acute Oral Toxicity Prediction with Automatic Chemical Feature Extraction[J]. Journal of Chemical Information and Modeling, 2017, 57(11):2672-2685[22] Coley C. W., Barzilay R., Green W. H., et al. Convolutional Embedding of Attributed Molecular Graphs for Physical Property Prediction[J]. Journal of Chemical Information and Modeling, 2017, 57(8):1757-1772 |