@article{SinghSinhaMishraetal.2022, author = {Singh, Manudeo and Sinha, Rajiv and Mishra, Arjit and Babu, Suresh}, title = {Wetlandscape (dis)connectivity and fragmentation in a large wetland (Haiderpur) in west Ganga plains, India}, series = {Earth surface processes and landforms : the journal of the British Geomorphological Research Group}, volume = {47}, journal = {Earth surface processes and landforms : the journal of the British Geomorphological Research Group}, number = {7}, publisher = {Wiley}, address = {New York, NY [u.a.]}, issn = {0197-9337}, doi = {10.1002/esp.5352}, pages = {1872 -- 1887}, year = {2022}, abstract = {Wetlands are dynamic ecosystems that require continuous monitoring and assessment of degradation status to design strategies for their sustainable management. While hydrology provides the primary functional control for the wetland ecosystem, the loss of landscape connectivity influences wetland degradation in a major way as it leads to fragmentation. This article aims to integrate hydrogeomorphic and ecological concepts for the assessment of degradation status and its causal factors for a large wetland in the western Ganga plains, India, the Haiderpur, using a wetlandscape approach. We have used a remote-sensing-based approach, which offers a powerful tool for assessing and linking cross-scale structures, functions, and controls in a wetlandscape. The Haiderpur, a Ramsar site since December 2021, is an artificial wetland located on the right bank of the Ganga River wherein the inflows are controlled by a barrage constructed on the Ganga River apart from smaller tributaries flowing in from the north. A novel aspect of this work is the integration of river dynamics and its connectivity to the wetlandscape to understand the spatiotemporal variability in the waterspread area in the wetland. In this work, we have developed an integrated wetlandscape assessment approach by evaluating wetland's geomorphic and hydrological connectivity status for the period 1993-2019 (25 years) across three different spatial scales - regional, catchment, and wetland. We have highlighted the ecological implications of connectivity and patch dynamics for developing sustainable wetland management plans.}, language = {en} } @article{SalertKruegerBagnichetal.2013, author = {Salert, Beatrice Ch. D. and Krueger, Hartmut and Bagnich, Sergey A. and Unger, Thomas and Jaiser, Frank and Al-Sa'di, Mahmoud and Neher, Dieter and Hayer, Anna and Eberle, Thomas}, title = {New polymer matrix system for phosphorescent organic light-emitting diodes and the role of the small molecular co-host}, series = {Journal of polymer science : A, Polymer chemistry}, volume = {51}, journal = {Journal of polymer science : A, Polymer chemistry}, number = {3}, publisher = {Wiley-Blackwell}, address = {Hoboken}, issn = {0887-624X}, doi = {10.1002/pola.26409}, pages = {601 -- 613}, year = {2013}, abstract = {A new matrix system for phosphorescent organic light-emitting diodes (OLEDs) based on an electron transporting component attached to an inert polymer backbone, an electronically neutral co-host, and a phosphorescent dye that serves as both emitter and hole conductor are presented. The inert co-host is used either as small molecules or covalently connected to the same chain as the electron-transporting host. The use of a small molecular inert co-host in the active layer is shown to be highly advantageous in comparison to a purely polymeric matrix bearing the same functionalities. Analysis of the dye phosphorescence decay in pure polymer, small molecular co-host film, and their blend lets to conclude that dye molecules distribute mostly in the small molecular co-host phase, where the co-host prevents agglomeration and self-quenching of the phosphorescence as well as energy transfer to the electron transporting units. In addition, the co-host accumulates at the anode interface where it acts as electron blocking layer and improves hole injection. This favorable phase separation between polymeric and small molecular components results in devices with efficiencies of about 47 cd/A at a luminance of 1000 cd/m(2). Investigation of OLED degradation demonstrates the presence of two time regimes: one fast component that leads to a strong decrease at short times followed by a slower decrease at longer times. Unlike the long time degradation, the efficiency loss that occurs at short times is reversible and can be recovered by annealing of the device at 180 degrees C. We also show that the long-time degradation must be related to a change of the optical and electrical bulk properties.}, language = {en} } @article{NeffeLoewenbergJulichGruneretal.2021, author = {Neffe, Axel T. and L{\"o}wenberg, Candy and Julich-Gruner, Konstanze K. and Behl, Marc and Lendlein, Andreas}, title = {Thermally-induced shape-memory behavior of degradable gelatin-based networks}, series = {International journal of molecular sciences}, volume = {22}, journal = {International journal of molecular sciences}, number = {11}, publisher = {Molecular Diversity Preservation International}, address = {Basel}, issn = {1422-0067}, doi = {10.3390/ijms22115892}, pages = {15}, year = {2021}, abstract = {Shape-memory hydrogels (SMH) are multifunctional, actively-moving polymers of interest in biomedicine. In loosely crosslinked polymer networks, gelatin chains may form triple helices, which can act as temporary net points in SMH, depending on the presence of salts. Here, we show programming and initiation of the shape-memory effect of such networks based on a thermomechanical process compatible with the physiological environment. The SMH were synthesized by reaction of glycidylmethacrylated gelatin with oligo(ethylene glycol) (OEG) alpha,omega-dithiols of varying crosslinker length and amount. Triple helicalization of gelatin chains is shown directly by wide-angle X-ray scattering and indirectly via the mechanical behavior at different temperatures. The ability to form triple helices increased with the molar mass of the crosslinker. Hydrogels had storage moduli of 0.27-23 kPa and Young's moduli of 215-360 kPa at 4 degrees C. The hydrogels were hydrolytically degradable, with full degradation to water-soluble products within one week at 37 degrees C and pH = 7.4. A thermally-induced shape-memory effect is demonstrated in bending as well as in compression tests, in which shape recovery with excellent shape-recovery rates R-r close to 100\% were observed. In the future, the material presented here could be applied, e.g., as self-anchoring devices mechanically resembling the extracellular matrix.}, language = {en} } @article{MachatschekSaretiaLendlein2021, author = {Machatschek, Rainhard Gabriel and Saretia, Shivam and Lendlein, Andreas}, title = {Assessing the influence of temperature-memory creation on the degradation of copolyesterurethanes in ultrathin films}, series = {Advanced materials interfaces}, volume = {8}, journal = {Advanced materials interfaces}, number = {6}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {2196-7350}, doi = {10.1002/admi.202001926}, pages = {8}, year = {2021}, abstract = {Copolyesterurethanes (PDLCLs) based on oligo(epsilon-caprolactone) (OCL) and oligo(omega-pentadecalactone) (OPDL) segments are biodegradable thermoplastic temperature-memory polymers. The temperature-memory capability in these polymers with crystallizable control units is implemented by a thermomechanical programming process causing alterations in the crystallite arrangement and chain organization. These morphological changes can potentially affect degradation. Initial observations on the macroscopic level inspire the hypothesis that switching of the controlling units causes an accelerated degradation of the material, resulting in programmable degradation by sequential coupling of functions. Hence, detailed degradation studies on Langmuir films of a PDLCL with 40 wt\% OPDL content are carried out under enzymatic catalysis. The temperature-memory creation procedure is mimicked by compression at different temperatures. The evolution of the chain organization and mechanical properties during the degradation process is investigated by means of polarization-modulated infrared reflection absorption spectroscopy, interfacial rheology and to some extend by X-ray reflectivity. The experiments on PDLCL Langmuir films imply that degradability is not enhanced by thermal switching, as the former depends on the temperature during cold programming. Nevertheless, the thin film experiments show that the leaching of OCL segments does not induce further crystallization of the OPDL segments, which is beneficial for a controlled and predictable degradation.}, language = {en} } @article{BarkowOswaldLensingetal.2020, author = {Barkow, Isolde S. and Oswald, Sascha and Lensing, Hermann Josef and Munz, Matthias}, title = {Seasonal dynamics modifies fate of oxygen, nitrate, and organic micropollutants during bank filtration}, series = {Environmental science and pollution research : official organ of the EuCheMS Division for Chemistry and the Environment, EuCheMS DCE}, volume = {28}, journal = {Environmental science and pollution research : official organ of the EuCheMS Division for Chemistry and the Environment, EuCheMS DCE}, number = {8}, publisher = {Springer}, address = {Heidelberg}, issn = {0944-1344}, doi = {10.1007/s11356-020-11002-9}, pages = {9682 -- 9700}, year = {2020}, abstract = {Bank filtration is considered to improve water quality through microbially mediated degradation of pollutants and is suitable for waterworks to increase their production. In particular, aquifer temperatures and oxygen supply have a great impact on many microbial processes. To investigate the temporal and spatial behavior of selected organic micropollutants during bank filtration in dependence of relevant biogeochemical conditions, we have set up a 2D reactive transport model using MODFLOW and PHT3D under the user interface ORTI3D. The considered 160-m-long transect ranges from the surface water to a groundwater extraction well of the adjacent waterworks. For this purpose, water levels, temperatures, and chemical parameters were regularly measured in the surface water and groundwater observation wells over one and a half years. To simulate the effect of seasonal temperature variations on microbial mediated degradation, we applied an empirical temperature factor, which yields a strong reduction of the degradation rate at groundwater temperatures below 11 degrees C. Except for acesulfame, the considered organic micropollutants are substantially degraded along their subsurface flow paths with maximum degradation rates in the range of 10(-6) mol L-1 s(-1). Preferential biodegradation of phenazone, diclofenac, and valsartan was found under oxic conditions, whereas carbamazepine and sulfamethoxazole were degraded under anoxic conditions. This study highlights the influence of seasonal variations in oxygen supply and temperature on the fate of organic micropollutants in surface water infiltrating into an aquifer.}, language = {en} }