579
170. Olivier-Bourbigou H, Forestière A, Saussine L, Magna L, Favre F, Hugues F (2010) Olefin
oligomerization for the production of fuels and petrochemicals. Oil Gas Eur Mag, 36:97−102.
https://www.osti.gov/etdeweb/biblio/21327984
171. Svejda SA, Brookhart M (1999) Ethylene oligomerization and propylene dimerization using
cationic (α-diimine) nickel(II) catalysts. Organometallics 18:65–74. https://doi.org/10.1021/
om980736t
172. Finiels A, Fajula F, Hulea V (2014) Nickel-based solid catalysts for ethylene oligomerization.
A review. Cat Sci Technol 4:2412–2426. https://doi.org/10.1039/C4CY00305E
173. Skupinska J (1991) Oligomerization of alpha-olefins to higher oligomers. Chem Rev
91:613–648. https://doi.org/10.1021/cr00004a007
174. Andrei RD, Popa MI, Fajula F, Hulea V (2015) Heterogeneous oligomerization of ethylene over highly active and stable Ni-AlSBA-15 mesoporous catalysts. J Catal 323:76–−84.
https://doi.org/10.1016/j.jcat.2014.12.027
175. Agirrezabal-Telleria I, Iglesia E (2017) Stabilization of active, selective, and regenerable
Ni-based dimerization catalysts by condensation of ethene within ordered mesopores. J Catal
352:505–514. https://doi.org/10.1016/j.jcat.2017.06.025
176. Mol JC (2004) Industrial applications of olefin metathesis. J Mol Catal A Chem 213:39–−45.
https://doi.org/10.1016/j.molcata.2003.10.049
177. Lwin S, Wachs IE (2014) Olefin metathesis by supported metal oxide catalysts. ACS Catal
4:2505–2520. https://doi.org/10.1021/cs500528h
178. Andrei RD, Popa MI, Cammarano C, Hulea V (2016) Nickel and molybdenum containing mesoporous catalysts for ethylene oligomerization and metathesis. New J Chem
40:4146–4152. https://doi.org/10.1039/C5NJ02586A
179. Andrei RD, Popa MI, Fajula F, Cammarano C, AlKhudhair A, Bouchmella K, Mutin PH,
Hulea V (2015) Ethylene to propylene by one-pot catalytic cascade reactions. ACS Catal
5:2774–2777. https://doi.org/10.1021/acscatal.5b00383
180. Lin B, Zhang Q, Wang Y (2009) Catalytic conversion of ethylene to propylene and butenes
over H-ZSM-5. Ind Eng Chem Res 48:10788−10795. https://doi.org/10.1021/ie901227p
181. Oikawa H, Shibata Y, Inazu K, Iwase Y, Murai K, Hyodo S, Kobayashi G, Baba T (2006)
Highly selective conversion of ethylene to propene over SAPO-34 as a solid acid catalyst.
Appl Catal A 312:181–185. https://doi.org/10.1016/j.apcata.2006.06.045
182. Song ZX, Takahashi A, Mimura N, Fujitani T (2009) Production of propylene from ethanol
over ZSM-5 zeolites. Catal Lett 131:364–369. https://doi.org/10.1007/s10562- 009- 0071- 3
183. Mizuno S, Kurosawa M, Tanaka M, Iwamoto M (2012) One-path and selective conversion
ethanol to propene on scandium-modified indium oxide catalysts. Chem Lett 41:892–894.
https://doi.org/10.1246/cl.2012.892
184. Iwamoto M (2011) One step formation of propene from ethene or ethanol through metathesis on nickel ion-loaded silica. Molecules 16:7844–7863. https://doi.org/10.3390/
molecules16097844
185. Nishiguchi T, Matsumoto T, Kanai H, Utani K, Matsumura Y, Shen WJ, Imamura S (2005)
Catalytic steam reforming of ethanol to produce hydrogen and acetone. Appl Catal A
2005(279):273–277. https://doi.org/10.1016/j.apcata.2004.10.035
186. Murthy RS, Patnaik P, Sidheswaran P, Jayamani M (1988) Conversion of ethanol to acetone over promoted iron oxide catalysis. J Catal 109:298–302. https://doi.
org/10.1016/0021- 9517(88)90212- 6
187. Nakajima T, Nameta H, Mishima S, Matsuzaki I, Tanabe KJ (1994) A highly active and
highly selective oxide catalyst for the conversion of ethanol to acetone in the presence of
water vapour. Mater Chem 4:853–−858. https://doi.org/10.1039/JM9940400853
188. Bussi J, Parodi S, Irigaray B, Kieffer R (1998) Catalytic transformation of ethanol into
Acetone using copper pyrochlore catalysts. Appl Catal A 172:117–129. https://doi.
org/10.1016/S0926- 860X(98)00106- 9
Catalytic Conversion of Alcohols into Value-Added Products
170. Olivier-Bourbigou H, Forestière A, Saussine L, Magna L, Favre F, Hugues F (2010) Olefin
oligomerization for the production of fuels and petrochemicals. Oil Gas Eur Mag, 36:97−102.
https://www.osti.gov/etdeweb/biblio/21327984
171. Svejda SA, Brookhart M (1999) Ethylene oligomerization and propylene dimerization using
cationic (α-diimine) nickel(II) catalysts. Organometallics 18:65–74. https://doi.org/10.1021/
om980736t
172. Finiels A, Fajula F, Hulea V (2014) Nickel-based solid catalysts for ethylene oligomerization.
A review. Cat Sci Technol 4:2412–2426. https://doi.org/10.1039/C4CY00305E
173. Skupinska J (1991) Oligomerization of alpha-olefins to higher oligomers. Chem Rev
91:613–648. https://doi.org/10.1021/cr00004a007
174. Andrei RD, Popa MI, Fajula F, Hulea V (2015) Heterogeneous oligomerization of ethylene over highly active and stable Ni-AlSBA-15 mesoporous catalysts. J Catal 323:76–−84.
https://doi.org/10.1016/j.jcat.2014.12.027
175. Agirrezabal-Telleria I, Iglesia E (2017) Stabilization of active, selective, and regenerable
Ni-based dimerization catalysts by condensation of ethene within ordered mesopores. J Catal
352:505–514. https://doi.org/10.1016/j.jcat.2017.06.025
176. Mol JC (2004) Industrial applications of olefin metathesis. J Mol Catal A Chem 213:39–−45.
https://doi.org/10.1016/j.molcata.2003.10.049
177. Lwin S, Wachs IE (2014) Olefin metathesis by supported metal oxide catalysts. ACS Catal
4:2505–2520. https://doi.org/10.1021/cs500528h
178. Andrei RD, Popa MI, Cammarano C, Hulea V (2016) Nickel and molybdenum containing mesoporous catalysts for ethylene oligomerization and metathesis. New J Chem
40:4146–4152. https://doi.org/10.1039/C5NJ02586A
179. Andrei RD, Popa MI, Fajula F, Cammarano C, AlKhudhair A, Bouchmella K, Mutin PH,
Hulea V (2015) Ethylene to propylene by one-pot catalytic cascade reactions. ACS Catal
5:2774–2777. https://doi.org/10.1021/acscatal.5b00383
180. Lin B, Zhang Q, Wang Y (2009) Catalytic conversion of ethylene to propylene and butenes
over H-ZSM-5. Ind Eng Chem Res 48:10788−10795. https://doi.org/10.1021/ie901227p
181. Oikawa H, Shibata Y, Inazu K, Iwase Y, Murai K, Hyodo S, Kobayashi G, Baba T (2006)
Highly selective conversion of ethylene to propene over SAPO-34 as a solid acid catalyst.
Appl Catal A 312:181–185. https://doi.org/10.1016/j.apcata.2006.06.045
182. Song ZX, Takahashi A, Mimura N, Fujitani T (2009) Production of propylene from ethanol
over ZSM-5 zeolites. Catal Lett 131:364–369. https://doi.org/10.1007/s10562- 009- 0071- 3
183. Mizuno S, Kurosawa M, Tanaka M, Iwamoto M (2012) One-path and selective conversion
ethanol to propene on scandium-modified indium oxide catalysts. Chem Lett 41:892–894.
https://doi.org/10.1246/cl.2012.892
184. Iwamoto M (2011) One step formation of propene from ethene or ethanol through metathesis on nickel ion-loaded silica. Molecules 16:7844–7863. https://doi.org/10.3390/
molecules16097844
185. Nishiguchi T, Matsumoto T, Kanai H, Utani K, Matsumura Y, Shen WJ, Imamura S (2005)
Catalytic steam reforming of ethanol to produce hydrogen and acetone. Appl Catal A
2005(279):273–277. https://doi.org/10.1016/j.apcata.2004.10.035
186. Murthy RS, Patnaik P, Sidheswaran P, Jayamani M (1988) Conversion of ethanol to acetone over promoted iron oxide catalysis. J Catal 109:298–302. https://doi.
org/10.1016/0021- 9517(88)90212- 6
187. Nakajima T, Nameta H, Mishima S, Matsuzaki I, Tanabe KJ (1994) A highly active and
highly selective oxide catalyst for the conversion of ethanol to acetone in the presence of
water vapour. Mater Chem 4:853–−858. https://doi.org/10.1039/JM9940400853
188. Bussi J, Parodi S, Irigaray B, Kieffer R (1998) Catalytic transformation of ethanol into
Acetone using copper pyrochlore catalysts. Appl Catal A 172:117–129. https://doi.
org/10.1016/S0926- 860X(98)00106- 9
Catalytic Conversion of Alcohols into Value-Added Products