Search Results
Reversibly compressible and freestanding monolithic carbon spherogels
2019, Salihovic, M., Zickler, G.A., Fritz-Popovski, G., Ulbricht, M., Paris, O., Hüsing, N., Presser, V., Elsaesser, M.S.
We present a versatile strategy to tailor the nanostructure of monolithic carbon aerogels. By use of an aqueous colloidal solution of polystyrene in the sol-gel processing of resorcinol-formaldehyde gels, we can prepare, after supercritical drying and successive carbonization, freestanding monolithic carbon aerogels, solely composed of interconnected and uniformly sized hollow spheres, which we name carbon spherogels. Each sphere is enclosed by a microporous carbon wall whose thickness can be adjusted by the polystyrene concentration, which affects the pore texture as well as the mechanical properties of the aerogel monolith. In this study, we used monodisperse polystyrene spheres of approximately 250 nm diameter, which result in an inner diameter of the final hollow carbon spheres of approximately 200 ± 5 nm due to shrinkage during the carbonization process. The excellent homogeneity of the samples, as well as uniform sphere geometries, are confirmed by small- and angle X-ray scattering. The presence of macropores between the hollow spheres creates a monolithic network with the benefit of being reversibly compressible up to 10% linear strain without destruction. Electrochemical tests demonstrate the applicability of ground and CO2 activated carbon spherogels as electrode materials. © 2019 The Authors
Understanding of water resilience in the Anthropocene
2019, Falkenmark, Malin, Wang-Erlandsson, Lan, Rockström, Johan
Water is indispensable for Earth resilience and sustainable development. The capacity of social-ecological systems to deal with shocks, adapting to changing conditions and transforming in situations of crisis are fundamentally dependent on the functions of water to e.g., regulate the Earth's climate, support biomass production, and supply water resources for human societies. However, massive, inter-connected, human interference involving climate forcing, water withdrawal, dam constructions, and land-use change have significantly disturbed these water functions and induced regime shifts in social-ecological systems. In many cases, changes in core water functions have pushed systems beyond tipping points and led to fundamental shifts in system feedback. Examples of such transgressions, where water has played a critical role, are collapse of aquatic systems beyond water quality and quantity thresholds, desertification due to soil and ecosystem degradation, and tropical forest dieback associated with self-amplifying moisture and carbon feedbacks. Here, we aggregate the volumes and flows of water involved in water functions globally, and review the evidence of freshwater related linear collapse and non-linear tipping points in ecological and social systems through the lens of resilience theory. Based on the literature review, we synthesize the role of water in mediating different types of ecosystem regime shifts, and generalize the process by which life support systems are at risk of collapsing due to loss of water functions. We conclude that water plays a fundamental role in providing social-ecological resilience, and suggest that further research is needed to understand how the erosion of water resilience at local and regional scale may potentially interact, cascade, or amplify through the complex, globally hyper-connected networks of the Anthropocene. © 2018 The Authors
EURODELTA III exercise: An evaluation of air quality models’ capacity to reproduce the carbonaceous aerosol
2019, Mircea, Mihaela, Bessagnet, Bertrand, D'Isidoro, Massimo, Pirovano, Guido, Aksoyoglu, Sebnem, Ciarelli, Giancarlo, Tsyro, Svetlana, Manders, Astrid, Bieser, Johannes, Stern, Rainer, Vivanco, Marta GarcÃa, Cuvelier, Cornelius, Aas, Wenche, Prévôt, André S.H., Aulinger, Armin, Briganti, Gino, Calori, Giuseppe, Cappelletti, Andrea, Colette, Augustin, Couvidat, Florian, Fagerli, Hilde, Finardi, Sandro, Kranenburg, Richard, Rouïl, Laurence, Silibello, Camillo, Spindler, Gerald, Poulain, Laurent, Herrmann, Hartmut, Jimenez, Jose L., Day, Douglas A., Tiitta, Petri, Carbone, Samara
The carbonaceous aerosol accounts for an important part of total aerosol mass, affects human health and climate through its effects on physical and chemical properties of the aerosol, yet the understanding of its atmospheric sources and sinks is still incomplete. This study shows the state-of-the-art in modelling carbonaceous aerosol over Europe by comparing simulations performed with seven chemical transport models (CTMs) currently in air quality assessments in Europe: CAMx, CHIMERE, CMAQ, EMEP/MSC-W, LOTOS-EUROS, MINNI and RCGC. The simulations were carried out in the framework of the EURODELTA III modelling exercise and were evaluated against field measurements from intensive campaigns of European Monitoring and Evaluation Programme (EMEP) and the European Integrated Project on Aerosol Cloud Climate and Air Quality Interactions (EUCAARI). Model simulations were performed over the same domain, using as much as possible the same input data and covering four seasons: summer (1–30 June 2006), winter (8 January – 4 February 2007), autumn (17 September- 15 October 2008) and spring (25 February - 26 March 2009). The analyses of models’ performances in prediction of elemental carbon (EC) for the four seasons and organic aerosol components (OA) for the last two seasons show that all models generally underestimate the measured concentrations. The maximum underestimation of EC is about 60% and up to about 80% for total organic matter (TOM). The underestimation of TOM outside of highly polluted area is a consequence of an underestimation of secondary organic aerosol (SOA), in particular of its main contributor: biogenic secondary aerosol (BSOA). This result is independent on the SOA modelling approach used and season. The concentrations and daily cycles of total primary organic matter (TPOM) are generally better reproduced by the models since they used the same anthropogenic emissions. However, the combination of emissions and model formulation leads to overestimate TPOM concentrations in 2009 for most of the models. All models capture relatively well the SOA daily cycles at rural stations mainly due to the spatial resolution used in the simulations. For the investigated carbonaceous aerosol compounds, the differences between the concentrations simulated by different models are lower than the differences between the concentrations simulated with a model for different seasons. © 2019 The Authors
Medical ethics in the Anthropocene: how are €100 billion of German physicians' pension funds invested?
2019, Schulz, Christian M., Ahrend, Klaus-Michael, Schneider, Gerhard, Hohendorf, Gerrit, Schellnhuber, Hans Joachim, Busse, Reinhard
[No abstract available]
Membrane Tension Orchestrates Rear Retraction in Matrix-Directed Cell Migration
2019, Hetmanski, J.H.R., de, Belly, H., Busnelli, I., Waring, T., Nair, R.V., Sokleva, V., Dobre, O., Cameron, A., Gauthier, N., Lamaze, C., Swift, J., del, Campo, A., Starborg, T., Zech, T., Goetz, J.G., Paluch, E.K., Schwartz, J.-M., Caswell, P.T.
In development, wound healing, and cancer metastasis, vertebrate cells move through 3D interstitial matrix, responding to chemical and physical guidance cues. Protrusion at the cell front has been extensively studied, but the retraction phase of the migration cycle is not well understood. Here, we show that fast-moving cells guided by matrix cues establish positive feedback control of rear retraction by sensing membrane tension. We reveal a mechanism of rear retraction in 3D matrix and durotaxis controlled by caveolae, which form in response to low membrane tension at the cell rear. Caveolae activate RhoA-ROCK1/PKN2 signaling via the RhoA guanidine nucleotide exchange factor (GEF) Ect2 to control local F-actin organization and contractility in this subcellular region and promote translocation of the cell rear. A positive feedback loop between cytoskeletal signaling and membrane tension leads to rapid retraction to complete the migration cycle in fast-moving cells, providing directional memory to drive persistent cell migration in complex matrices. © 2019 The AuthorsCell migration through 3D matrix is critical to developmental and disease processes, but the mechanisms that control rear retraction are poorly understood. Hetmanski et al. show that differential membrane tension allows caveolae to form at the rear of migrating cells and activate the contractile actin cytoskeleton to promote rapid retraction. © 2019 The Authors
Electrodeposition of Sr-substituted hydroxyapatite on low modulus beta-type Ti-45Nb and effect on in vitro Sr release and cell response
2019, Schmidt, Romy, Gebert, Annett, Schumacher, Matthias, Hoffmann, Volker, Voss, Andrea, Pilz, Stefan, Uhlemann, Margitta, Lode, Anja, Gelinsky, Michael
Beta-type Ti-based alloys are promising new materials for bone implants owing to their excellent mechanical biofunctionality and biocompatibility. For treatment of fractures in case of systemic diseases like osteoporosis the generation of implant surfaces which actively support the problematic bone healing is a most important aspect. This work aimed at developing suitable approaches for electrodeposition of Sr-substituted hydroxyapatite (Srx-HAp) coatings onto Ti-45Nb. Potentiodynamic polarization measurements in electrolytes with 1.67 mmol/L Ca(NO3)2, which was substituted by 0, 10, 50 and 100% Sr(NO3)2, and 1 mmol/L NH4H2PO4 at 333 K revealed the basic reaction steps for OH– and PO4 3− formation needed for the chemical precipitation of Srx-HAp. Studies under potentiostatic control confirmed that partial or complete substitution of Ca2+- by Sr2+-ions in solution has a significant effect on the complex reaction process. High Sr2+-ion contents yield intermediate phases and a subsequent growth of more refined Srx-HAp coatings. Upon galvanostatic pulse-deposition higher reaction rates are controlled and in all electrolytes very fine needle-like crystalline coatings are obtained. With XRD the incorporation of Sr-species in the hexagonal HAp lattice is evidenced. Coatings formed in electrolytes with 10 and 50% Sr-nitrate were chemically analyzed with EDX mapping and GD-OES depth profiling. Only a fraction of the Sr-ions in solution is incorporated into the Srx-HAp coatings. Therein, the Sr-distribution is laterally homogeneous but non-homogeneous along the cross-section. Increasing Sr-content retards the coating thickness growth. Most promising coatings formed in the electrolyte with 10% Sr-nitrate were employed for Ca, P and Sr release analysis in Tris-Buffered Saline (150 mM NaCl, pH 7.6) at 310 K. At a sample surface: solution volume ratio of 1:200, after 24 h the amount of released Sr-ions was about 30–35% of that determined in the deposited Srx-HAp coating. In vitro studies with human bone marrow stromal cells (hBMSC) revealed that the released Sr-ions led to a significantly enhanced cell proliferation and osteogenic differentiation and that the Sr-HAp surface supported cell adhesion indicating its excellent cytocompatibility. © 2019 The Authors
Energy system changes in 1.5 °C, well below 2 °C and 2 °C scenarios
2019, Gambhir, Ajay, Rogelj, Joeri, Luderer, Gunnar, Few, Sheridan, Napp, Tamaryn
Meeting the Paris Agreement's goal to limit global warming to well below 2 °C and pursuing efforts towards 1.5 °C is likely to require more rapid and fundamental energy system changes than the previously-agreed 2 °C target. Here we assess over 200 integrated assessment model scenarios which achieve 2 °C and well-below 2 °C targets, drawn from the IPCC's fifth assessment report database combined with a set of 1.5 °C scenarios produced in recent years. We specifically assess differences in a range of near-term indicators describing CO2 emissions reductions pathways, changes in primary energy and final energy across the economy's major sectors, in addition to more detailed metrics around the use of carbon capture and storage (CCS), negative emissions, low-carbon electricity and hydrogen. © 2018 The Authors
Switchable double-sided micropatterned adhesives for selective fixation and detachment
2019, Tinnemann, V., Arzt, E., Hensel, R.
Micropatterned dry adhesives are promising candidates for the development of innovative adhesive platforms. Their reversible adhesion to various materials and surfaces has been reported over more than a decade. Switching between a strong and a weak adhesive state can be introduced by elastic buckling instabilities of the microstructure. In this work, we report on novel adhesive pads that exhibit micropatterned pillars on both sides. In double-sided PDMS micropatterns, the dimensions of the pillar structures were tuned by modulating the critical force for buckling during compressive loading. In this way, selective detachment of glass substrates was induced from one side of the pad. Our results indicate a significant switching efficiency of up to 83% between the strong and weak adhesive state. The new structures have high potential for emerging applications where temporary, double-sided fixations in combination with a predetermined detachment location are required. © 2018
Opinion paper : Measuring livestock robustness and resilience : are we on the right track?
2019, Llonch, P., Hoffmann, G., Bodas, R., Mirbach, D., Verwer, C., Haskell, M.J.
[No abstract available]
Redox-electrolytes for non-flow electrochemical energy storage: A critical review and best practice
2019, Lee, J., Srimuk, P., Fleischmann, S., Su, X., Hatton, T.A., Presser, V.
Over recent decades, a new type of electric energy storage system has emerged with the principle that the electric charge can be stored not only at the interface between the electrode and the electrolyte but also in the bulk electrolyte by redox activities of the electrolyte itself. Those redox electrolytes are promising for non-flow hybrid energy storage systems, or redox electrolyte-aided hybrid energy storage (REHES) systems; particularly, when they are combined with highly porous carbon electrodes. In this review paper, critical design considerations for the REHES systems are discussed as well as the effective electrochemical characterization techniques. Appropriate evaluation of the electrochemical performance is discussed thoroughly, including advanced analytical techniques for the determination of the electrochemical stability of the redox electrolytes and self-discharge rate. Additionally, critical summary tables for the recent progress on REHES systems are provided. Furthermore, the unique synergistic combination of porous carbon materials and redox electrolytes is introduced in terms of the diffusion, adsorption, and electrochemical kinetics modulating energy storage in REHES systems. © 2018 The Author(s)