Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Juha Keskiväli"'
Autor:
Arttu Lamberg, Arpad Toldy, Juha Keskiväli, Anna Karvo, Martti Larmi, Annukka Santasalo-Aarnio
Publikováno v:
SAE Technical Paper Series.
Autor:
Kristian Rönn, Andre Swarts, Vickey Kalaskar, Terry Alger, Rupali Tripathi, Juha Keskiväli, Ossi Kaario, Annukka Santasalo-Aarnio, Rolf Reitz, Martti Larmi
Publikováno v:
Progress in Energy and Combustion Science. 95:101064
Funding Information: The authors want to thank the support by the Dean’s grant of Aalto University School of Engineering , Henry Ford Foundation of Finland and Technology Industries of Finland, Combustion Engines Branch Group. Publisher Copyright:
Autor:
Pekka Simell, Matti Reinikainen, Matti Putkonen, Laura Keskiväli, Noora Kaisalo, Timo Repo, Juha Keskiväli, Päivi Aakko-Saksa
Publikováno v:
Simell, P, Reinikainen, M, Putkonen, M, Keskiväli, L, Kaisalo, N, Repo, T, Keskiväli, J & Aakko-Saksa, P May. 07 2020, Catalyst for dehydrogenation, method for preparing the catalyst and use, Patent No. FI20185940 .
VTT Technical Research Centre of Finland-PURE
VTT Technical Research Centre of Finland-PURE
The invention relates to a catalyst for dehydrogenation. The catalyst is a Pt catalyst, in which Pt catalyst agent is formed by using a Pt-precursor and is arranged on a support, and the support is selected from TiO2 or gamma-?12O3. Further, the inve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::362435dae6530fcf1e24d13b1355209f
https://cris.vtt.fi/en/publications/7edad701-7f6c-4719-9ac1-ad4227f80202
https://cris.vtt.fi/en/publications/7edad701-7f6c-4719-9ac1-ad4227f80202
Publikováno v:
ChemCatChem. 10:2908-2914
A homogeneous Mn(NO3)(2)/2,2,6,6-tetramethylpiperidin-1-yl)oxyl/2-picolinic acid catalyst system is highly active and versatile for the selective aerobic oxidation of alcohols (2,2,6,6-tet-ramethylpiperidin-1-yl)oxyl = TEMPO, 2-picolinic acid = PyCOO
Publikováno v:
RSC Advances. 8:15111-15118
Herein, we report an efficient transition metal triflate catalyzed approach to convert biomass-based compounds, such as monoterpene alcohols, sugar alcohols, octyl acetate and tea tree oil, to their corresponding olefins in high yields. The reaction
Publikováno v:
ChemCatChem. 9:4244-4255
5-Hydroxymethylfurfural (HMF) constitutes one of the pivotal chemicals to utilize biomass as chemical feedstock. For this approach the vast majority of methods require accessing to pure HMF from biomass before its utilization, thus incorporating one
Autor:
Timo Repo, Kalle Lagerblom, Konstantin Chernichenko, Vladimir Iashin, Juha Keskiväli, Pauli Wrigstedt
Publikováno v:
European Journal of Organic Chemistry. 2017:880-891
Autor:
Teemu T. T. Myllymäki, Marko Vehkamäki, Jaakko Pekka Karjalainen, Kristoffer Meinander, Timo Repo, Sari Rautiainen, Juha Keskiväli, Kalle Lagerblom, Marianna Kemell, Mikko Heikkilä
Publikováno v:
GREEN CHEMISTRY. 19(19):4563-4570
Herein, we describe an efficient two-step pathway for isosorbide synthesis from cellulose with the use of new recyclable Ru-catalysts. We show that the oxidative and sulfonation treatments of the new Ru-catalysts increase the acidity and the hydrophi
Publikováno v:
ChemCatChem. 7:501-507
The effect of salts and Bronsted acids on the Lewis acid (CrCl3⋅6 H2O)-catalyzed glucose dehydration to 5-hydroxymethylfurfural (HMF) in aqueous media are described. We show that the reaction with bromide salts in place of chlorides leads to higher
Solvent-free NaOH catalyzed aldol condensation of biomass-derived 5-hydroxymethyl furfural (HMF) and furfural with methyl isobutyl ketone (MIBK) was studied, producing branched C-11 and C-12 furan compounds in high yields of up to 96%. Through use of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7529ab536a38ceae627c7b8eaf0153be
http://hdl.handle.net/10138/300365
http://hdl.handle.net/10138/300365