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Technologielösungen für hocheffiziente zero-emission H2-Motoren für KWK-Anwendungen, Teilvorhaben: AS3 'keramische Kolbenringe'

Das übergeordnete Ziel des Forschungsprojekts Technologielösungen für hocheffiziente zero-emission H2-Motoren für KWK-Anwendungen (CH2P) ist es, Kraft-Wärme-Kopplungsanlagen (KWK-Anlagen) hundertprozentig mit Wasserstoff zu betreiben und dabei wirtschaftlich konkurrenzfähig zu Erdgas betriebenen Anlagen zu sein. Die Technologie befindet sich derzeit auf einem TRL von 3-4 und soll durch die Projektarbeiten mit dem Fokus auf unterschiedlichen Teilbereichen der Motoren auf ein TRL von 6-7 angehoben werden. Einer wichtiger Baustein innerhalb des Projektes ist die Entwicklung keramischer Kolbenringe. Kolbenringe sind hochbelastete Bauteile eines Verbrennungsmotors, denen die Aufgabe der Abdichtung des Arbeitsraumes zufällt. Die hohe Flammgeschwindigkeit bei der Verbrennung von H2 führt zu hohen Temperaturen an der Zylinderwand und im Bereich der Kolbenringe (Tmax ca. 250 - 300 °C). Dadurch kommt es zu einer Austrocknung des Ölfilms an der Zylinderwand und zu einem hohen Verschleiß von konventionellen, metallischen Kolbenringen. Durch den Ansatz faserverstärkte Keramiken - speziell C/C-SiC - soll die Abdichtung des Brennraums verbessert und eine deutlich höhere Verschleißbeständigkeit erzielt werden. Ungebundener amorpher Kohlenstoff innerhalb des Werkstoffes wirkt sich zudem positiv als schmierfähiger Feststoff auf das Gleitverhalten aus. Durch die so erzielte verminderte Reibung wird erneut der Verschleiß reduziert. Die so beschriebenen Werkstoffeigenschaften sollen zusätzlich mit einer Faserverstärkung kombiniert werden, welche eine elastische Ringweitung und -kompression erlaubt. Um die Herstellung solcher keramischen Ringe zu erreichen, sind die im Arbeitsplan beschrieben Aktivitäten notwendig.

Climate-neutral Circular Economy enabled by Digital Product Carbon Pass, Teilvorhaben: Umsetzung im betrieblichen Umfeld bei Lorenz

Optimierung der CO2-Bilanz, Ressourceneffizienz und Recyclingfähigkeit von Leichtbauteilen aus Kunststoff durch Entwicklung und Verbreitung eines datenbankgestützten Softwaretools

SP 1.5 Molekulare Charakterisierung von gelösten organischen Stoffen in der Meeresoberflächen-Mikroschicht (SML) und deren Einfluss auf den anorganischen Kohlenstoffkreislauf

Unsere Motivation ist es, die Rolle von gelöstem organischem Material (DOM) in marinen Oberflächenfilmen (SML) als eine Schlüsselkomponente zu verstehen, die den Gasaustausch zwischen Atmosphäre und Meer, die Karbonatchemie, sowie die Ökophysiologie der assoziierten Organismen beeinflusst (Engel et al., 2017). Während unserer Vorarbeiten haben wir Hinweise auf einen bisher unbekannten Zusammenhang zwischen DOM und Karbonatchemie in der SML gefunden, sowie auf eine hohe räumlich-zeitliche Dynamik in der DOM-Zusammensetzung. Obwohl die hohe Heterogenität des SML-DOM-Geometabolom (d.h. die Gesamtheit des DOM-Pools, der durch biotische und abiotische Prozesse produziert und modifiziert wird) bekannt ist, gibt es wenige detaillierte Studien darüber. Insgesamt gibt es noch kein mechanistisches Verständnis darüber, unter welchen Bedingungen DOM in der SML in verschiedene chemische Fraktionen aufgeteilt wird. Dies liegt an der derzeit geringen Verfügbarkeit von Daten von einer größeren Anzahl von Untersuchungsstandorten unter unterschiedlichen Umwelt- und Versuchsbedingungen, sowie an einen Mangel an interdisziplinären Studien, die Physik, Geochemie und Biologie kombinieren. Mit anderen Worten, uns fehlen grundlegende (organo-)geochemische Informationen von der größten Luft-Wasser-Grenzfläche der Erde, mit unbekannten Konsequenzen für den damit verbundenen Austausch von klimarelevanten Gasen. In diesem Projekt streben wir an, diese Lücke durch sich ergänzende Messungen der DOM-Zusammensetzung und anorganischer Kohlenstoff-Systemparameter zu schließen. Die Relevanz für die Forschungseinheit BASS ergibt sich aus dem Ziel unseres Teilprojekts, die fehlenden grundlegenden biogeochemischen Informationen des SML-DOM-Inventars zur Verfügung zu stellen und sie in den Kontext der Ökosystemprozesse in der SML zu setzen, einschließlich der DOM-Produktion (SP1.1) sowie des mikrobiellen (SP1.2) und photochemischen (SP1.4) Umsatzes. Darüber hinaus werden wir den Beitrag des DOM-Geometaboloms zum Säure-Basen-Gleichgewicht der SML untersuchen, von dem wir erwarten, dass es die Gasgleichgewichte in der Grenzfläche - insbesondere im Kohlensäuresystem und damit auch die Treibhausgasflüsse - beeinflusst (SP2.1).

Integration von Totholz in Verfahren der Direktsaat von Weißtanne (Abies alba) und Stiel-Eiche (Quercus robur) zur Begründung stabiler, klimatoleranter Mischwaldökosysteme im Stadtwald Hildburghausen

Verwertung des Aufwuchses von vernässtem Grünland für die Erzeugung von regenerativer Energie sowie Kohlen zur CO2-Speicherung, Teilvorhaben: Stoffstromanalyse, Prozessentwicklung und Analytik sowie ökonomische und ökobilanzielle Bewertung

Species level size-normalised weight data for at depth analysis

This dataset contains a compilation of published and new SNW data with corresponding environmental data extracted from CMIP6 that are used in the at depth species level Bayesian regression modelling. Environmental data for G. truncatulinoides comes from 200m depth, all other environmental data is from the sea surface (≤ 20 m).

Field based and laboratory data of sediment cores from the Lower Havel Inner Delta near Lake Gülpe, Brandenburg (Germany)

Sediment cores were recovered using a hand-held Cobra Pro (Atlas Copco) core drilling system with a 60 mm diameter open corer. One-meter segments were retrieved and assessed in the field for sedimentological features, including estimations of grain size, carbonate content, humus content, and redox features (AG Boden 2005, 2024). Colour descriptions were carried out using the Munsell Soil Color Chart. The exact positions of the drilling points were recorded using a differential GPS device (TOPCON HiPer II). The cores were photographed, documented and sampled at 5–10 cm intervals for subsequent laboratory analyses. Bulk samples from five selected cores (RK1, RK3, RK13, RK15, RK17) were freeze-dried, sieved (2 mm), and weighed. Total carbon (TC), total nitrogen (TN), and total sulfur (TS) contents were measured using a CNS analyzer (Vario EL cube, Elementar). Inorganic carbon (TIC) was determined using calcimeter measurements (Scheibler method, Eijkelkamp). Organic carbon (TOC) was calculated as TOC = TC − TIC. For the grain size analyses, sediment samples were first sieved to <2 mm and subsamples of 10 g were treated with 50 ml of 35% hydrogen peroxide (H₂O₂) and gently heated to remove organic matter. Following this, 10 ml of 0.4 N sodium pyrophosphate solution (Na₄P₂O₇) was added to disperse the particles, and the suspension was subjected to ultrasonic treatment for 45 minutes. The sand fraction was analysed by dry sieving and classified into four size classes: coarse sand (2000–630 µm), medium sand (630–200 µm), fine sand (200–125 µm), and very fine sand (125–63 µm). Finer fractions were determined using X-ray granulometry (XRG) with a SediGraph III 5120 (Micromeritics). These included coarse silt (63–20 µm), medium silt (20–6.3 µm), fine silt (6.3–2.0 µm), coarse clay (2.0–0.6 µm), medium clay (0.6–0.2 µm), and fine clay (<0.2 µm).

Geophysical, Sedimentological and Geochemical Data from the Lower Havel Inner Delta (Gülpe Island), Brandenburg (Germany)

To investigate subsurface features in the Lower Havel River floodplain, we conducted Electrical Resistivity Tomography (ERT) transects and Electromagnetic Induction (EMI) surveys at three different depths in 2023 and 2024. These near surface geophysical methods were complemented by 24 driving core drillings to relate the electrical properties with sedimentological characteristics. Additionally, five selected sediment cores were used for subsequent geochemical lab analyses (grain size, CNS, TOC, TIC). Electromagnetic induction (EMI) was measured with a CMD-Mini Explorer (GF Instruments s.r.o., Brno, Czech Republic) in June 2023 and June 2024. We used the vertical dipole (VDP) at coil spacings of 0.32 m (VDP1), 0.71 m (VDP2) and 1.18 m (VDP3), archieving effective penetration depths of 0.5 m (VDP1), 1.0 m (VDP2) and 1.8 m (VDP3). According to the manufacturer, 70% of the signal originate from above these depths. The EMI sensors measure the apparent electrical conductivity (ECa, in mS/m). Measurements were taken by carrying the instrument about 0.2 m above ground while being directly connected to D-GPS (Leica GPS1200) for positioning. The acquisition rate was five measurements per second. Data quality was checked by measuring a reference line before and after each measurement. The area investigated by EMI in June 2023 is located to the north and northeast of the Gülpe research station. It has a total area of 12.3 ha. The reference line was located in the southern part of the study area. No drift correction had to be applied due to good data quality. Reference lines and single outliers were removed. The area investigated by EMI in June 2024 is located southeast of the research station. The survey area there is 8.1 ha in size. The reference line for the measurements there was located in the north-westernmost area of the site. No drift correction had to be applied due to good data quality. Reference lines and single outliers were removed. The Electrical Resistivity Tomography (ERT) data were acquired by using a PC controlled DC resistivity meter system (RESECS, Geoserve, Kiel, Germany). In total, we measured four ERT transects. Two transects in June 2023, where transect 1 had a total length of 259 m with an electrode spacing of 0.5 m and transect 2 had a total length of 223 m with an electrode spacing of 1 m. The measurements in 2023 were carried out under extreme dry conditions. Two further transects were measured in June 2024 with an electrode spacing of 1m, transect 3 with a total length of 207 m and transect 4 with a total length of 239 m. We applied wenner alpha and dipol-dipol configuration. The coordinates and the height of the electrodes were measured with a D-GPS (2023: TOPCON HiPer II / 2024: Leica GPS1200). Sediment cores were recovered using a hand-held Cobra Pro (Atlas Copco) core drilling system with a 60 mm diameter open corer. One-meter segments were retrieved and assessed in the field for sedimentological features, including estimations of grain size, carbonate content, humus content, and redox features (AG Boden 2005, 2024). Colour descriptions were carried out using the Munsell Soil Color Chart. The exact positions of the drilling points were recorded using a differential GPS device (TOPCON HiPer II). The cores were photographed, documented and sampled at 5–10 cm intervals for subsequent laboratory analyses. Bulk samples from five selected cores (RK1, RK3, RK13, RK15, RK17) were freeze-dried, sieved (2 mm), and weighed. Total carbon (TC), total nitrogen (TN), and total sulfur (TS) contents were measured using a CNS analyzer (Vario EL cube, Elementar). Inorganic carbon (TIC) was determined using calcimeter measurements (Scheibler method, Eijkelkamp). Organic carbon (TOC) was calculated as TOC = TC − TIC. For the grain size analyses, sediment samples were first sieved to <2 mm and subsamples of 10 g were treated with 50 ml of 35% hydrogen peroxide (H₂O₂) and gently heated to remove organic matter. Following this, 10 ml of 0.4 N sodium pyrophosphate solution (Na₄P₂O₇) was added to disperse the particles, and the suspension was subjected to ultrasonic treatment for 45 minutes. The sand fraction was analysed by dry sieving and classified into four size classes: coarse sand (2000–630 µm), medium sand (630–200 µm), fine sand (200–125 µm), and very fine sand (125–63 µm). Finer fractions were determined using X-ray granulometry (XRG) with a SediGraph III 5120 (Micromeritics). These included coarse silt (63–20 µm), medium silt (20–6.3 µm), fine silt (6.3–2.0 µm), coarse clay (2.0–0.6 µm), medium clay (0.6–0.2 µm), and fine clay (<0.2 µm).

(Table A1) Raw data for both AMT20 Atlantic Ocean transect samples and western Pacific Ocean transect (SO228 and SO256) samples

Sea surface salinity (SSS) is the least constrained major variable of the past (paleo) ocean but is fundamental in controlling the density of seawater and thus large-scale ocean circulation. The hydrogen isotopic composition (δD) of non-exchangeable hydrogen of algal lipids, specifically alkenones, has been proposed as a promising new proxy for paleo SSS. The δD of surface seawater is correlated with SSS, and laboratory culture studies have shown the δD of algal growth water to be reflected in the δD of alkenones. However, a large-scale field study testing the validity of this proxy is still lacking. Here we present the δD of open-ocean Atlantic and Pacific surface waters and coincident δD of alkenones sampled by underway filtration. Two transects of approximately 100° latitude in the Atlantic Ocean and more than 50° latitude in the Western Pacific sample much of the range of open ocean salinities and seawater δD, and thus allow probing the relationship between δD of seawater and alkenones. Overall, the open ocean δD alkenone data correlate significantly with SSS, and also agree remarkably well with δD water vs δD alkenone regressions developed from culture studies. Subtle deviations from these regressions are discussed in the context of physiological factors as recorded in the carbon isotopic composition of alkenones. In a best-case scenario, the data presented here suggest that SSS variations as low as 1.2 can be reconstructed from alkenone δD.

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