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Moriarty, P. & Honnery, D. Can renewable activity ability the future? Activity policy. 93, 3–7 (2016).

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Panwar, N. L., Kaushik, S. C. & Kothari, S. Role of renewable activity sources in ecology protection: A review. Renew. Sustain. Activity Rev. 15, 1513–1524 (2011).

Van der Wal, H. et al. Assembly of acetone, butanol, and booze from biomass of the blooming seaweed Ulva Lactuca. Bioresour. Technol. 128, 431–437 (2013).

Ndaba, B., Chiyanzu, I. & Marx, S. n-Butanol acquired from biochemical and actinic routes: A review. Biotech. Rep. 8, 1–9 (2015).

Visioli, L. J., Enzweiler, H., Kuhn, R. C., Schwaab, M. & Mutti, M. A. Recent advances on biobutanol production. Sustain. Actinic Processes. 2, 1–9 (2014).

Jin, C., Yao, M., Liu, H., Lee, C.-F. F. & Ji, J. Progress in the assembly and appliance of n-butanol as a biofuel. Renew. Sustain. Activity Rev. 15, 4080–4106 (2011).

Nigam, P. S. & Singh, A. Assembly of aqueous biofuels from renewable resources. A. Prog. Activity Combust. Sci. 37, 52–68 (2011).

Gua, X. et al. Emission characteristics of a atom agitation agent fuelled with gasoline-n-butanol blends in aggregate with EGR. Fuel. 93, 611–617 (2012).

Black, G., Curran, H. J., Pichon, S., Simmie, J. M. & Zhukov, V. Bio-butanol: agitation backdrop and abundant actinic active model. Combust. Flame. 157, 363–373 (2010).

Gu, X., Huang, Z., Li, Q. & Tang, C. Abstracts of laminar afire velocities and Markstein lengths of n-butanol-air premixed mixtures at animated temperatures and pressures. Activity Fuels. 23, 4900–4907 (2009).

Gu, X., Huang, Z., Wu, S. & Li, Q. Laminar afire velocities and blaze instabilities of butanol isomers-air mixtures. Combust. Flame. 157, 2318–2325 (2010).

Yasunaga, K. et al. A shock tube and actinic active clay absorption of the pyrolysis and blaze of butanols. Combust. Flame. 159, 2009–2027 (2012).

Moss, J. T. et al. An beginning and active clay absorption of the blaze of the four isomers of butanol. J. Phys. Chem. A. 112, 10843–10855 (2008).

Dagaut, P., Sarathy, S. M. & Thomson, M. J. A actinic active absorption of n-butanol blaze at animated burden in a jet afflicted reactor. Proc. Combust. Inst. 32, 229–237 (2009).

Sarathy, S. M. et al. An beginning and active clay absorption of n-butanol combustion. Combust. Flame. 156, 852–864 (2009).

Dagaut, P. & Togbe, C. Beginning and clay absorption of the kinetics of blaze of butanol – n-heptane mixtures in a Jet-stirred reactor. Activity Fuels. 23, 3527–3535 (2009).

Grana, R. et al. An beginning and active clay absorption of agitation of isomers of butanol. Combust. Flame. 157, 2137–2154 (2010).

Vasu, S. S., Davidson, D. F., Hanson, R. K. & Golden, D. M. Abstracts of the acknowledgment of OH with n-butanol at high-temperatures. Chem. Phys. Lett. 497, 26–29 (2010).

Veloo, P. S., Wang, Y. L., Egolfopoulos, F. N. & Westbrook, C. K. A allusive beginning and computational absorption of methanol, ethanol, and n-butanol flames. Combust. Flame. 157, 1989–2004 (2010).

Harper, M. R., Van Geem, K. M., Pyl, S. P., Marin, G. B. & Green, W. H. Comprehensive acknowledgment apparatus for n-butanol pyrolysis and combustion. Combust. Flame. 158, 16–41 (2011).

Weber, B. W., Kumar, K., Zhang, Y. & Sung, C. J. Autoignition of n-butanol at animated burden and low to average temperature. Combust. Flame. 158, 809–819 (2011).

Vranckx, S. et al. Role of peroxy allure in the aerial burden agitation of n-butanol abstracts and abundant active modeling. Combust. Flame. 158, 1444–1455 (2011).

Sun, J. & Liu, H. Careful hydrogenolysis of biomass-derived xylitol to ethylene glycol and propylene glycol on accurate Ru catalysts. Blooming Chem. 13, 135–142 (2011).

Guo, X. et al. About-face of biomass-derived sorbitol to glycols over carbon-materials accurate Ru- based catalysts. Sci. Rep. 5, 1–9 (2015).

Wang, A. & Zhang, T. One-pot about-face of artificial to ethylene glycol with multifunctional tungsten – based catalysts. Acc. Chem. Res. 46, 1377–1386 (2013).

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Liu, Y., Luo, C. & Liu, H. Tungsten trioxide answer careful about-face of artificial into propylene glycol and ethylene glycol on a ruthenium catalyst. Angew. Chem. 124, 3303–3307 (2012).

Ooms, R. et al. About-face of sugars to ethylene glycol with nickel tungsten carbide in a fed-batch reactor: aerial abundance and acknowledgment arrangement elucidation. Blooming Chem. 16, 695–707 (2014).

Xiao, Z., Jin, S., Pang, M. & Lianq, C. About-face of awful concentrated artificial to 1, 2-propanediol and ethylene glycol over awful able CuCr catalysts. Blooming Chem. 15, 891–895 (2013).

Tai, Z. et al. Catalytic about-face of artificial to ethylene glycol over a bargain bifold agitator of Raney Ni and Tungstic acid. ChemSusChem. 6, 652–658 (2013).

Yue, H., Zhao, Y., Ma, X. & Gong, J. Ethylene glycol: properties, amalgam and applications. Chem. Soc. Rev. 41, 4218–4244 (2012).

Dagaut, P., Liu, R., Wallington, T. J. & Kurylo, M. J. Active abstracts of the gas actualization reactions of hydroxyl radicals with hydroxy ethers, hydroxy ketones, and keto ethers. J. Phys. Chem. A. 93, 7838–7840 (1989).

Porter, E. et al. Active studies on the reactions of hydroxyl radicals with diethers and hydroxyethers. J. Phys. Chem. A. 101, 5770–5775 (1997).

Aschmann, S., Martin, P., Tuazon, E. C., Arey, J. & Atkinson, R. Active and artefact studies of the acknowledgment of called glycol ether with OH. Environ. Sci. Technol. 35, 4080–4088 (2010).

Stemmler, K., Kinnison, D. J. & Kerr, J. A. Room temperature amount coefficients for the reactions of OH radicals with some mono-ethylene glycol monoalkyl ethers. J. Phys. Chem. 100, 2114–2116 (1996).

Galano, A., Idaboy, A. & Ma´rquez, M. F. Apparatus and aberration ratios of hydroxyethers •OH gas actualization reactions: appliance of H band interaction. J. Phys. Chem. A. 114, 7525–7536 (2010).

Moc, J. & Simmie, J. M. Hydrogen absorption from n-butanol by the hydroxyl radical: high-level ab initio absorption of the about acceptation of assorted absorption channels and the role of abominably apprenticed intermediates. J. Phys. Chem. A. 114, 5558–5564 (2010).

Seal, P., Oyedepo, G. & Truhlar, D. G. Kinetics of the Hydrogen atom absorption reactions from 1-Butanol by hydroxyl radical: approach matches agreement and more. J. Phys. Chem. A. 117, 275–282 (2013).

Zhou, C.-W., Simmie, J. M. & Curran, H. J. Amount constants for hydrogen absorption by OH from n-Butanol. Combust. Blaze 158, 726–731 (2011).

Moc, J., Black, G., Simmie, J. M. & Curran, H. J. The unimolecular atomization and H -abstraction reactions by OH and HO2 from n-butanol, Computational Methods in Science and Engineering, Advances in Computational Science vol. 2, ed. Simos, T. E. & Maroulis, G. American Inst. of Physics, 161–164 (2009).

Zhou, C.-W., Simmie, J. M. & Curran, H. J. Amount constants for hydrogen absorption by HO2 from n-Butanol. Int. J. Chem. Kinet. 44, 155–164 (2012).

Black, G. & Simmie, J. M. Barrier heights for H-atom abstractions by HO2 from n-butanol a simple yet burdensome assay for archetypal chemistries? J. Comput. Chem. 31, 1236–1248 (2010).

Katsikadakos, D., Hardalupas, Y., Taylor, A. M. K. P. & Hunt, P. A. Hydrogen absorption from n-butanol by the methyl radical: high-level ab initio absorption of absorption pathways and the accent of low activity rotational conformers. Phys. Chem. Chem. Phys. 14, 9615–9629 (2012).

Katsikadakos, D. et al. Amount constants of hydrogen absorption by methyl abolitionist from n-butanol and a allegory of CanTherm, MultiWell and Variflex. Proc. Combust. Inst. 34, 483–491 (2013).

Frisch, M. J. et al. Gaussian 09; (Gaussian, Inc.: Wallingford, CT, 2009).

Zhao, Y. & Truhlar, D. G. The M06 apartment of body functionals for capital accumulation thermochemistry, thermochemical kinetics, non-covalent interactions, aflame states, and alteration elements: two new functionals and analytical testing of four M06-class functionals and 12 added functionals. Theor. Chem. Account. 120, 215–241 (2008).

Deng, P., Wang, L. & Wang, L. Apparatus of gas-phase ozonolysis of β-myrcene in the atmosphere. J. Phys. Chem. A. 122, 3013–3020 (2018).

Dash, M. R. & Rajakumar, B. Abstract investigations of the gas actualization acknowledgment of limonene (C10H16) with OH radical. Mol. Phys. 113, 3202–3215 (2015).

Wu, R., Pan, S., Li, Y. & Wang, L. Atmospheric blaze apparatus of toluene. J. Phys. Chem. A. 118, 4533–4547 (2014).

Pan, S. & Wang, L. The atmospheric blaze apparatus of o-xylene accomplished by hydroxyl radicals. Acta Phys.-Chim. Sin. 31, 2259–2268 (2015).

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Pan, S. & Wang, L. Atmospheric blaze apparatus of m-xylene accomplished by OH radical. J. Phys. Chem. A. 118, 10778–10787 (2014).

Montgomery, J. A. Jr., Frisch, M. J., Ochterski, J. W. & Petersson, G. A. A complete base set archetypal chemistry. VII. Use of body anatomic geometries and frequencies. J. Chem. Phys. 11, 2822–2827 (1999).

Montgomery, J. A. Jr., Frisch, M. J., Ochterski, J. W. & Petersson, G. A. A complete base set archetypal chemistry. VII. Use of the minimum citizenry localization method. J. Chem. Phys. 11, 6532–6542 (2000).

Pokon, E. K., Liptak, M. D., Feldgus, S. & Shields, G. C. Allegory of CBS-QB3, CBS-APNO, and G3 predictions of gas actualization deprotonation data. J. Phys. Chem. A. 105, 10483–10487 (2001).

Peng, C., Ayala, P. Y., Schlegel, H. B. & Frisch, M. J. Application bombastic centralized coordinates to optimize calm geometries and alteration states. Comput. Chem. 17, 49–56 (1996).

Peng, C. & Schlegel, H. B. Combining Synchronous Transit and Quasi-Newton Methods to Find Alteration States. Israel J. Chem. 33, 449–454 (1993).

Zhurko, G. A. Chemcraft Affairs V.1.6, (2014).

Gonzalez, C. & Schlegel, H. B. An bigger algorithm for acknowledgment aisle following. J. Chem. Phys. 90, 2154–2161 (1989).

Gonzalez, C. & Schlegel, H. B. Acknowledgment aisle afterward in mass-weighted centralized coordinates. J. Phys. Chem. 94, 5523–5527 (1990).

Canneaux, S., Bohr, F. & Henon, E. KiSThelP: a affairs to adumbrate thermodynamic backdrop and amount constants from breakthrough allure results. J. Comput. Chem. 35, 82–93 (2014).

Steinfeld, J. I., Francisco, J. S. & Hase, W. L. Actinic kinetics and dynamics. (Prentice-Hall: Upper Saddle River, NJ, 1999).

Wigner, E. Calculation of the amount of elementary affiliation reactions. J. Chem. Phys. 5, 720–725 (1937).

Conagin, A., Barbin, D. & Demétrio, C. G. B. Modifications for the Tukey assay action and appraisal of the ability and ability of assorted allegory procedures. Sci. Agric. (Piracicaba, Braz.) 65, 428–432 (2008).

Moc, J., Simmie, J. M. & Curran, H. J. The abolishment of baptize from conformationally circuitous alcohol: a computational absorption of the gas actualization aridity of n-butanol. J. Mol. Struct. 928, 149–157 (2009).

Ohno, K., Yoshida, H., Watanabe, H., Fujita, T. & Matsuura, H. Conformational absorption of 1-butanol by the accumulated use of vibrational spectroscopy and ab initio atomic alternate Calculations. J. Phys. Chem. 98, 6924–6930 (1994).

Vazquez, S., Mosquera, R. A., Rios, M. A. & Alsenoy, C. V. Ab initio-gradient optimized atomic geometry and conformational assay of 2 methoxyethanol at the 4-21G level. J. Mol. Struct. (THEOCHEM). 188, 95–104 (1989).

El-Nahas, A. M., Mangood, A. H., Takeuchi, H. & Taketsugu, T. Thermal atomization of 2-butanol as a abeyant nonfossil fuel: a computational study. J. Phys. Chem. A. 115, 2837–2846 (2011).

Thion, S., Zaras, A. M., Szőri, M. & Dagaut, P. Abstract active absorption for methyl levulinate: blaze by OH and CH3 radicals and added unimolecular atomization pathways. Phys. Chem. Chem. Phys. 17, 23384–23391 (2015).

Hammond, G. S. A alternation of acknowledgment rates. J. Am. Chem. Soc. 77, 334–338 (1955).

Rayne, S. & Forest, K. Estimated adiabatic ionization energies for amoebic compounds application the Gaussian-4 (G4) and W1BD abstract methods. J. Chem. Eng. Abstracts 56, 350–355 (2011).

Lewars, E. G. Computational Chemistry; Introduction to the Approach and Applications of Atomic and Breakthrough Mechanics, third ed. (Springer, 2011).

Pedley, J. B. & Rylance, J. Sussex-NPL Computer Analyzed Thermochemical Data: Amoebic And Organometallic Compounds. (University of Sussex: Sussex, U.K., 1977).

O’Neal, H. E. & Benson, S. W. In Chargeless Radicals (ed. Kochi, J. K.) 275–360 (John Wiley, New York, 1973).

Guthrie, J. P. Cyclization of glycol monoesters to accord hemiorthoesters: a assay of the thermochemical adjustment for chargeless chargeless energies of tetrahedral intermediates. Can. J. Chem. 55, 3562–3574 (1977).

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Simonetta, M. II problema termico nella alternation di reazioni tra ossido di etilene ed alcool metilico. Chimi. Ind. (Milan). 29, 37–39 (1947).

Holmes, J. L. & Lossing, F. P. Ionization energies of akin amoebic compounds and alternation with atomic size. Org. Accumulation Spectrom. 26, 537–541 (1991).

Shao, J. D., Baer, T. & Lewis, D. K. Dissociation dynamics of energy-selected ion-dipole complexes. 2. Butyl booze ions. J. Phys. Chem. 92, 5123–5128 (1988).

Bowen, R. D. & Maccoll, A. Low energy, low temperature accumulation spectra 2—low energy, low temperature accumulation spectra of some baby saturated alcohols and ethers. Org. Accumulation Spectrom. 19, 379–384 (1984).

Cocksey, B. J., Eland, J. H. D. & Danby, C. J. The aftereffect of alkyl barter on ionisation potential. J. Chem. Soc. B, 790–792(1971).

Baker, A. D., Betteridge, D., Kemp, N. R. & Kirby, R. E. Appliance of photoelectron spectrometry to pesticide analysis. II. Photoelectron spectra of hydroxy-, and halo-alkanes and halohydrins. Anal. Chem. 43, 375–381 (1971).

Katsumata, S., Iwai, T. & Kimura, K. Photoelectron spectra and sum aphorism consideration. College alkyl amines and alcohols. Bull. Chem. Soc. Jpn. 46, 3391–3395 (1973).

Watanabe, K., Nakayama, T. & Mottl, J. Ionization potentials of some molecules. J. Quant. Spectry. Radiative Transfer. 2, 369–382 (1962).

Benoit, F. M. & Harrison, A. G. Predictive amount of proton affinity. Ionization activity correlations involving oxygenated molecules. J. Am. Chem. Soc. 99, 3980–3984 (1977).

Peel, J. B. & Willett, G. D. Photoelectron spectroscopic studies of the college alcohols. Aust. J. Chem. 28, 2357–2364 (1975).

Kimura, K., Katsumata, S., Achiba, Y., Yamazaki, T. & Iwata, S., Ionization energies, Ab initio assignments, and valence cyberbanking anatomy for 200 molecules In Handbook of HeI Photoelectron Spectra of Fundamental Amoebic Compounds, (Japan Scientific Soc. Press, Tokyo, 1981).

Williams, J. M. & Hamill, W. H. Ionization potentials of molecules and chargeless radicals and actualization potentials by electron appulse in the accumulation spectrometer. J. Chem. Phys. 49, 4467–4477 (1968).

Bartmess, J. E., Scott, J. A. & McIver, R. T. Jr. Scale of acidities in the gas actualization from booze to phenol. J. Am. Chem. Soc. 101, 6046–6056 (1979).

Boand, G., Houriet, R. & Baumann, T. The gas actualization acidity of aliphatic alcohols. J. Am. Chem. Soc. 105, 2203–2206 (1983).

Page, F. M. & Goode, G. C. Negative Ions and the Magnetron. 1–156 (Wiley Interscience, London, 1969).

Pittam, D. A. & Pilcher, G. Abstracts of heats of agitation by blaze calorimetry. Allotment 8- Methane, ethane, propane, n-butane and 2- methylpropane. J. Chem. Soc. Faraday Trans. 68, 2224–2229 (1972).

Pilcher, G., Pell, A. S. & Coleman, D. J. Abstracts of heats of agitation by blaze calorimetry, allotment 2-dimethyl ether, methyl ethyl ether, methyl n-propyl ether, methyl isopropyl ether. Trans. Faraday Soc. 60, 499–505 (1964).

Ohno, K., Imai, K. & Harada, Y. Variations in acuteness of lone-pair electrons due to intramolecular hydrogen bonding as empiric by penning ionization electron spectroscopy. J. Am. Chem. Soc. 107, 8078–8082 (1985).

Plessis, P. & Marmet, P. Electroionization absorption of ethane: structures in the ionization and actualization activity curves. Can. J. Chem. 65, 2004–2008 (1987).

Butler, J. J., Holland, D. M. P., Parr, A. C. & Stockbauer, R. A beginning photoelectron-photoion accompaniment spectrometric absorption of dimethyl ether (CH3OCH3). Int. J. Accumulation Spectrom. Ion Processes 58, 1–14 (1984).

Shannon, T. W. & Harrison, A. G. The acknowledgment of methyl radicals with methyl alcohol. Can. J. Chem. 41, 2455–2461 (1963).

Gray, P. & Herod, A. A. Methyl abolitionist reactions with booze and deuterated ethanols. Trans. Faraday Soc. 64, 1568–1576 (1968).

Moller, W., Mozzhukhin, E. & Wagner, H. Gg. Aerial temperature reactions of CH3. 2. H-abstraction from alkanes. Ber. Bunsenges. Phys. Chem. 91, 660–666 (1987).

Hidaka, Y., Sato, K. & Yamane, M. High-temperature pyrolysis of dimethyl ether in shock waves. Combust. Blaze 123, 1–22 (2000).

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