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One-step flame synthesis of SnO<sub>2</sub>/TiO<sub>2</sub> composite nanoparticles for photocatalytic applications
Akurati, K. K., Vital, A., Hany, R., Bommer, B., Graule, T., & Winterer, M. (2005). One-step flame synthesis of SnO2/TiO2 composite nanoparticles for photocatalytic applications. International Journal of Photoenergy, 7(4), 153-161. https://doi.org/10.1155/S1110662x05000231
Chemical synthesis and characterization of POSS-functionalized poly[3-hydroxyalkanoates]
Hany, R., Hartmann, R., Böhlen, C., Brandenberger, S., Kawada, J., Löwe, C., … Marchessault, R. H. (2005). Chemical synthesis and characterization of POSS-functionalized poly[3-hydroxyalkanoates]. Polymer, 46(14), 5025-5031. https://doi.org/10.1016/j.polymer.2005.04.020
Tailored material properties of polyhydroxyalkanoates through biosynthesis and chemical modification
Zinn, M., & Hany, R. (2005). Tailored material properties of polyhydroxyalkanoates through biosynthesis and chemical modification. Advanced Engineering Materials, 7(5), 408-411. https://doi.org/10.1002/adem.200500053
Gasoline composition determined by 1H NMR spectroscopy
Burri, J., Crockett, R., Hany, R., & Rentsch, D. (2004). Gasoline composition determined by 1H NMR spectroscopy. Fuel, 83(2), 187-193. https://doi.org/10.1016/S0016-2361(03)00261-8
Encapsulated zosteric acid embedded in poly[3-hydroxyalkanoate] coatings - protection against biofouling
Geiger, T., Delavy, P., Hany, R., Schleuniger, J., & Zinn, M. (2004). Encapsulated zosteric acid embedded in poly[3-hydroxyalkanoate] coatings - protection against biofouling. Polymer Bulletin, 52(1), 65-72. https://doi.org/10.1007/s00289-004-0253-5
Chemical synthesis of crystalline comb polymers from olefinic medium-chain-length poly[3-hydroxyalkanoates]
Hany, R., Böhlen, C., Geiger, T., Hartmann, R., Kawada, J., Schmid, M., … Marchessault, R. H. (2004). Chemical synthesis of crystalline comb polymers from olefinic medium-chain-length poly[3-hydroxyalkanoates]. Macromolecules, 37(2), 385-389. https://doi.org/10.1021/ma0304426
Toward non-toxic antifouling: synthesis of hydroxy-, cinnamic acid-, sulfate-, and zosteric acid-labeled poly[3-hydroxyalkanoates]
Hany, R., Böhlen, C., Geiger, T., Schmid, M., & Zinn, M. (2004). Toward non-toxic antifouling: synthesis of hydroxy-, cinnamic acid-, sulfate-, and zosteric acid-labeled poly[3-hydroxyalkanoates]. Biomacromolecules, 5(4), 1452-1456. https://doi.org/10.1021/bm049962e
Tailored biosynthesis of olefinic medium-chain-length poly[(<i>R</i>)-3-hydroxyalkanoates] in <i>pseudomonas putida</i> GPo1 with improved thermal properties
Hartmann, R., Hany, R., Geiger, T., Egli, T., Witholt, B., & Zinn, M. (2004). Tailored biosynthesis of olefinic medium-chain-length poly[(R)-3-hydroxyalkanoates] in pseudomonas putida GPo1 with improved thermal properties. Macromolecules, 37(18), 6780-6785. https://doi.org/10.1021/ma040035+
Tailor-made synthesis of polyhydroxyalkanoate
Zinn, M., Hartmann, R., Noger, D., Pletscher, E., Ren, Q., Wüthrich, J., & Hany, R. (2004). Tailor-made synthesis of polyhydroxyalkanoate. Bio World, 9(3), 4-5.
Improved reproducibility of chemical reactions on purified polystyrene resins monitored by <sup>31</sup>P MAS NMR
Rentsch, D., Hany, R., Barthélémy, S., & Steinauer, R. (2003). Improved reproducibility of chemical reactions on purified polystyrene resins monitored by 31P MAS NMR. Tetrahedron Letters, 44(37), 6987-6990. https://doi.org/10.1016/S0040-4039(03)01803-3
Quantitative determination of loadings and oxidation products of polystyrene-bound phosphines using <sup>31</sup>P MAS NMR
Rentsch, D., Hany, R., Barthélémy, S., & Steinauer, R. (2003). Quantitative determination of loadings and oxidation products of polystyrene-bound phosphines using 31P MAS NMR. Journal of Combinatorial Chemistry, 5(5), 610-616. https://doi.org/10.1021/cc030004a
Tailored synthesis of poly([<i>R</i>]-3-hydroxybutyrate-<i>co</i>-3-hydroxyvalerate) (PHB/HV) in <i>Ralstonia eutropha</i> DSM 428
Zinn, M., Weilenmann, H. U., Hany, R., Schmid, M., & Egli, T. (2003). Tailored synthesis of poly([R]-3-hydroxybutyrate-co-3-hydroxyvalerate) (PHB/HV) in Ralstonia eutropha DSM 428. Acta Biotechnologica, 23(2-3), 309-316. https://doi.org/10.1002/abio.200390039
Preparation and characterization of enantiomerically pure telechelic diols from mcl-poly[(<i>R</i>)-3-hydroxyalkanoates]
Andrade, A. P., Witholt, B., Hany, R., Egli, T., & Li, Z. (2002). Preparation and characterization of enantiomerically pure telechelic diols from mcl-poly[(R)-3-hydroxyalkanoates]. Macromolecules, 35(3), 684-689. https://doi.org/10.1021/ma011420r
Synthesis and characterization of novel copoly(ester-urethane) containing blocks of poly-[(<i>R</i>)-3-hydroxyoctanoate] and poly-[(<i>R</i>)-3-hydroxybutyrate]
Andrade, A. P., Neuenschwander, P., Hany, R., Egli, T., Witholt, B., & Li, Z. (2002). Synthesis and characterization of novel copoly(ester-urethane) containing blocks of poly-[(R)-3-hydroxyoctanoate] and poly-[(R)-3-hydroxybutyrate]. Macromolecules, 35(13), 4946-4950. https://doi.org/10.1021/ma012223v
'DOK' long-term farming systems trial: microbial biomass, activity and diversity affect the decomposition of plant residues
Fliessbach, A., Eyhorn, F., Mäder, P., Rentsch, D. I., & Hany, R. (2001). 'DOK' long-term farming systems trial: microbial biomass, activity and diversity affect the decomposition of plant residues. In R. M. Rees, B. C. Ball, C. D. Campbell, & C. A. Watson (Eds.), Sustainable management of soil organic matter. Proceedings of the 27th meeting of the British society of soil science (pp. 363-369). https://doi.org/10.1079/9780851994659.0343
Quantitative Deuterium-NMR-Spektroskopie zur Echtheitsbestimmung von Naturstoffen
Hany, R., & Rentsch, D. (2001). Quantitative Deuterium-NMR-Spektroskopie zur Echtheitsbestimmung von Naturstoffen. In W. Muster & K. Schläpfer (Eds.), Nachhaltige Material- und Systemtechnik. Festschrift zum 65. Geburtstag von Fritz Eggimann (pp. 293-300). Empa.
Quantitative determination of resin loading in solid-phase organic synthesis using <sup>13</sup>C MAS NMR
Hany, R., Rentsch, D., Dhanapal, B., & Obrecht, D. (2001). Quantitative determination of resin loading in solid-phase organic synthesis using 13C MAS NMR. Journal of Combinatorial Chemistry, 3(1), 85-89. https://doi.org/10.1021/cc000066q
Biotransformation of various substituted aromatic compounds to chiral dihydrodihydroxy derivatives
Raschke, H., Meier, M., Burken, J. G., Hany, R., Müller, M. D., van der Meer, J. R., & Kohler, H. P. E. (2001). Biotransformation of various substituted aromatic compounds to chiral dihydrodihydroxy derivatives. Applied and Environmental Microbiology, 67(8), 3333-3339. https://doi.org/10.1128/AEM.67.8.3333-3339.2001
Comment on influence of the chemical environment on metolachlor conformations
Buser, H. R., Hany, R., Müller, M. D., Poiger, T., & Rentsch, D. (2000). Comment on influence of the chemical environment on metolachlor conformations. Journal of Agricultural and Food Chemistry, 48(9), 4448-4449. https://doi.org/10.1021/jf0005420
Investigation of base oils from various sources, used for the production of ACEA conforming motor oils
Hany, R., & Jäckle, H. W. (2000). Investigation of base oils from various sources, used for the production of ACEA conforming motor oils. In W. J. Bartz (Ed.), Tribology 2000 - plus. Volume I (pp. 323-324). Technische Akademie Esslingen.