Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Simon Trosien"'
Autor:
Mareike Zieglowski, Simon Trosien, Jochen Rohrer, Sabrina Mehlhase, Simone Weber, Kerstin Bartels, Gregor Siegert, Taina Trellenkamp, Karsten Albe, Markus Biesalski
Publikováno v:
Frontiers in Chemistry, Vol 7 (2019)
Using isocyanate-functionalized Kraft lignin as a reactive macromonomer for the preparation of polyurethane foams by a prepolymer technique is a well-known strategy to incorporate the biomacromolecule into a higher value polymer material. However, as
Externí odkaz:
https://doaj.org/article/55f450c027ee4a48a33042a053df6b20
Publikováno v:
Frontiers in Chemistry, Vol 7 (2019)
Chemistry, geometric shape and swelling behavior are the key parameters that determine any successful use of man-made polymeric networks (gels). While understanding of the swelling behavior of both water-swellable hydrogels and organogels that swell
Externí odkaz:
https://doaj.org/article/5a6374edbd7a405ba6a1baa765ce15fc
Publikováno v:
Frontiers in Chemistry, Vol 6 (2018)
Due to its unique material properties, paper offers many practical advantages as a viable platform for sensing devices. In view of paper-based microfluidic biosensing applications, the covalent immobilization of enzymes with preserved functional acti
Externí odkaz:
https://doaj.org/article/c34a4d4ecc5c4ec999dc8c250ea98016
Publikováno v:
ACS Materials Letters. 2:336-357
In recent years, Janus interface materials with wettability contrast have attracted remarkable attention because of their beneficial properties and versatile potential applications in materials sci...
Autor:
Robert W. Stark, Tobias Meckel, Andreas Geissler, Maximilian Nau, Martin J. Bitsch, Simon Trosien, Sascha Mehlhase, Brigitte Hertel, Christian Dietz, Marcus W. Ott, Gregor Siegert, Jasmin Huong, Markus Biesalski
Publikováno v:
Holzforschung
Holzforschung, De Gruyter, 2021, 75 (4), pp.390-398. ⟨10.1515/HF-2020-0060⟩
Holzforschung, De Gruyter, 2021, 75 (4), pp.390-398. ⟨10.1515/HF-2020-0060⟩
To improve the reactivity of lignin for incorporation into high value polymers, the introduction of amines via Mannich reaction is a commonly used strategy. During this functionalization reaction, intra- as well as intermolecular lignin–lignin cros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6481d63cf455de45c9956af020a83568
https://hal.archives-ouvertes.fr/hal-03251069
https://hal.archives-ouvertes.fr/hal-03251069
Autor:
Simone Weber, Gregor Siegert, Kerstin Bartels, Taina Trellenkamp, Karsten Albe, Markus Biesalski, Simon Trosien, Sascha Mehlhase, Mareike Zieglowski, Jochen Rohrer
Publikováno v:
Frontiers in Chemistry
Frontiers in Chemistry, Vol 7 (2019)
Frontiers in Chemistry, Vol 7 (2019)
Using isocyanate-functionalized Kraft lignin as a reactive macromonomer for the preparation of polyurethane foams by a prepolymer technique is a well-known strategy to incorporate the biomacromolecule into a higher value polymer material. However, as
Publikováno v:
Carbohydrate Polymers. 254:117458
Secondary hydroxyl groups of hydroxypropyl cellulose (HPC) are transformed into reactive carbonyl groups selectively via TEMPO-mediated oxidation in the presence of sodium hypochlorite. By using this oxidation protocol, we introduced carbonyl functio
Publikováno v:
RSC Advances. 6:109514-109518
Photochromic paper was prepared by covalent immobilisation of functional polymer networks with spiropyran moieties on paper sheets. The chromatic response of spiropyran molecules in the system can be dynamically controlled by simple damping technique
Publikováno v:
ACS applied materialsinterfaces. 10(43)
We introduce the design of Janus-type paper sheets where one side of the paper exhibits superhydrophobic properties, whereas the other side of the sheet remains hydrophilic and therefore can take up aqueous solutions by capillary wicking. Such papers
Autor:
Lara Schulz, Moritz Schubert, Simon Trosien, Dieter Schollmeyer, Carolin Brandscheid, Siegfried R. Waldvogel
Publikováno v:
European Journal of Organic Chemistry. 2014:7091-7094
Oxidative coupling by using molybdenum pentachloride provides fast and modular access to sophisticated thienoacenes in excellent yields. The coupling process can be accomplished with thiophene and benzothiophene derivatives and provides various compl