Zobrazeno 1 - 10
of 43
pro vyhledávání: '"M. A. Sanz-Tejedor"'
Publikováno v:
Renewable Energy. 164:1133-1142
This work presents the combustion results of a vegetable oils blend in a low-pressure auxiliary air fluid pulverisation burner (o emulsion burner). This blend was prepared from soy and sunflower refined vegetable oils (54.4%) and sunflower and rapese
Publikováno v:
Energy & Fuels. 32:11502-11510
This work presents the experimental results from refined palm vegetable oil atomization and combustion processes in a low-pressure auxiliary air fluid pulverization burner. The physicochemical properties that define palm vegetable oil as a fuel (dens
Publikováno v:
UVaDOC. Repositorio Documental de la Universidad de Valladolid
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This work experimentally investigates the combustion characteristics of refined soya, sunflower, and rapeseed vegetable oils and, by means of statistical techniques, determines the optimal operating factors of an emulsion burner to obtain the best co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffe42255f8d60d17f9f10616f06e1b70
https://doi.org/10.1021/acs.energyfuels.9b02003
https://doi.org/10.1021/acs.energyfuels.9b02003
Publikováno v:
Energy & Fuels. 30:7357-7366
This work presents experimental studies performed on a low-pressure auxiliary air fluid pulverization burner fueled with refined vegetable oils to research the impact of the fatty acid profile on combustion and regulated emissions. The vegetable oils
Publikováno v:
Fuel Processing Technology. 130:20-30
The use of vegetable oils as a fuel in burners is an alternative which offers certain advantages over the use of vegetable oils in engines. The present work explores the use of four oils: rapeseed, sunflower, soya, and a commercial mixture-seed as he
Publikováno v:
Chemistry - A European Journal. 18:5314-5318
Asymmetric nucleophilic monofluoroalkylation of a broad range of aldehydes with an α-fluoro-γ-sulfinylbenzyl carbanion takes place with complete control of the facial selectivity at the carbanion and good to high anti-diastereoselectivity to give e
Publikováno v:
Organic Letters. 13:4534-4537
Enantiomerically pure syn-1,2-diaryl-1,2-sulfanylamine derivatives can be obtained in a completely stereoselective manner by reaction of the benzylcarbanion Li-(S)-1 with N-phenyl (or PMP)-arylidene aldimines and further desulfinylation with t-BuLi.
Autor:
Inés Alonso, José L. García Ruano, Angela Meana, J. Felix Rodriguez, Yolanda Arroyo, M. Ascensión Sanz-Tejedor
Publikováno v:
The Journal of Organic Chemistry. 74:4217-4224
(R)-N-sulfinylimine and (S)-N-sulfinylimine react with the ylide derived from (S)-dimethyl-[2-(p-toluenesulfinyl)phenyl]sulfonium salt, affording trans-2,3-disubstituted aziridines. A complete trans selectivity in low facial diastereoselectivity is o
Publikováno v:
Organic Letters. 10:2151-2154
Alkylidenation of arylmethyl, dialkyl, and cyclic ketones with 2-(p-toluenesulfinyl)benzyl iodide in the presence of NaN(SiMe3)2 takes place with a high or complete control of the facial selectivity at the carbonyl group (up to 98% de) and the carban
Autor:
Alejandro Parra, M. Ascensión Sanz-Tejedor, Yolanda Arroyo, Inés Alonso, Jose Luis Garcia Ruano
Publikováno v:
ChemInform. 46
Fluorinated 2-(p-tolylsulfinyl)benzyl carbanions react with allyl and propargyl halides in a highly stereoselective way, providing homoallylic and homopropargylic fluorides, respectively, with high optical purity. Theoretical calculations found trans