TY - JOUR A1 - Roduner, E. A1 - Kaim, W. A1 - Sarkar, B. A1 - Urlacher, V.B. A1 - Pleiss, J. A1 - Gläser, R. A1 - Einicke, W.-D. A1 - Sprenger, G.A. A1 - Beifuß, U. A1 - Klemm, E. A1 - Liebner, Christian A1 - Hieronymus, Hartmut A1 - Hsu, S.-F. A1 - Plietker, B. A1 - Laschat, s. T1 - Selective catalytic oxidation of C-H bonds with molecular oxygen JF - ChemCatChem N2 - Although catalytic reductions, cross-couplings, metathesis, and oxidation of C=C double bonds are well established, the corresponding catalytic hydroxylations of C–H bonds in alkanes, arenes, or benzylic (allylic) positions, particularly with O2, the cheapest, 'greenest', and most abundant oxidant, are severely lacking. Certainly, some promising examples in homogenous and heterogenous catalysis exist, as well as enzymes that can perform catalytic aerobic oxidations on various substrates, but these have never achieved an industrial-scale, owing to a low space-time-yield and poor stability. This review illustrates recent advances in aerobic oxidation catalysis by discussing selected examples, and aims to stimulate further exciting work in this area. Theoretical work on catalyst precursors, resting states, and elementary steps, as well as model reactions complemented by spectroscopic studies provide detailed insight into the molecular mechanisms of oxidation catalyses and pave the way for preparative applications. However, O2 also poses a safety hazard, especially when used for large scale reactions, therefore sophisticated methodologies have been developed to minimize these risks and to allow convenient transfer onto industrial scale. KW - Coupling reactions KW - Feedstocks KW - Hydroxylation KW - Molecular oxygen KW - Oxidation KW - Catalytic oxidation KW - Micro reactor KW - Explosion KW - Safety PY - 2013 DO - https://doi.org/10.1002/cctc.201200266 SN - 1867-3880 VL - 5 IS - 1 SP - 82 EP - 112 PB - Wiley-VCH CY - Weinheim AN - OPUS4-27637 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Liebner, Christian A1 - Fischer, J. A1 - Heinrich, Sebastian A1 - Lange, T. A1 - Hieronymus, Hartmut A1 - Klemm, E. T1 - Are micro reactors inherently safe? An investigation of gas phase explosion propagation limits on ethene mixtures JF - Process safety and environmental protection N2 - A method for the determination of safety properties for micro reactors and micro structured components is presented. Micro structured reactors are not inherently safe but the range of safe operating conditions of micro reactors are extended since the explosion region is reduced. The λ/3 rule was demonstrated to be applicable to micro scale tubes for stoichiometric mixtures of ethane–oxygen and ethane–nitrous oxide. Furthermore first results from an investigation concerning detonation propagation through a micro reactor of non-ideal geometry are shown. Initial pressure investigated is ranging from low pressure up to 100 kPa. KW - Micro reactor KW - Explosion propagation limits KW - Chemical safety KW - Investigation method PY - 2012 DO - https://doi.org/10.1016/j.psep.2011.08.006 SN - 0957-5820 SN - 1744-3598 VL - 90 IS - 2 SP - 77 EP - 82 PB - Elsevier CY - Amsterdam AN - OPUS4-25594 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -