Transition-metal chemistry in ionic liquids (IL) has achieved intrinsic fascination in the last few years. The use of an IL as environmental friendly solvent, offers many advantages over traditional materials synthesis methods. The change from molecular to ionic reaction media leads to new types of materials being accessible. Room-temperature IL have been found to be excellent media for stabilising transition-metal clusters in solution and to crystallise homo- and heteronuclear transition-metal complexes and clusters. Furthermore, the use of IL as solvent provides the option to replace high-temperature routes, such as crystallisation from the melt or gas-phase deposition, by convenient room- or low-temperature syntheses. Inorganic IL composed of alkali metal cations and polynuclear transition-metal cluster anions are also known. Each of these areas will be discussed briefly in this contribution. / Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich.

Ionic liquids (ILs) have made a great impact on materials science and are being explored for potential applications in several disciplines. In this article, we briefly highlight the current state-of-the-art techniques employing ILs as new crystallisation media, working as neutral solvent, template or charge compensating species. The use of an IL as environmental friendly solvent offers many advantages over traditional crystallisation methods. The change from molecular to ionic reaction media leads to new types of materials being accessible. Room temperature ILs have been found to be excellent solvent systems for the crystallisation of a wide range of substances and morphologies ranging from nanoscopic crystals to micro- and even to macroscopic crystals. Moreover, high temperature routes, such as crystallisation from melts or gas phase deposition, have been replaced by convenient room or low temperature syntheses, employing ILs as reaction media. / Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich.

Die elektrokatalytische Wasserspaltung gilt als die nachhaltigste und sauberste Technologie zur Produktion von H2. Leider wird die Effizienz durch die träge Kinetik der Sauerstoffentwicklungsreaktion (OER) an der Anode stark eingeschränkt. Im Gegensatz zur OER ist die Elektrooxidation organischer Stoffe (EOO) thermodynamisch und kinetisch günstiger. Daher hat sich die Kopplung der EOO mit der Wasserstoffentwicklungsreaktion (HER) als Alternative herauskristallisiert, weil dabei die katalytische Effizienz für die H2-Produktion erheblich verbessert werden kann. Gleichzeitig können hochwertige organische Verbindungen an der Anode durch Verbesserung der Elektrooxidation erzeugt werden. In diesem Kurzaufsatz werden die aktuellsten Fortschritte und Meilensteine, die bereits bei der Kopplung der EOO mit der HER erzielt wurden, vorgestellt. Der Fokus liegt auf dem Design des Anodenkatalysators, dem Verständnis des Reaktionsmechanismus und der Konstruktion des Elektrolyseurs. Darüber hinaus werden Herausforderungen und Perspektiven in Bezug auf die künftige Entwicklung dieser innovativen Technologie aufgezeigt.

Due to utilization increase of chemical fertilizers and manures and of a large water volume for irrigation, agricultural runoff has significantly accelerated water pollution. The Red River locates in Vietnam where agriculture plays an important role in the country’s economy. This paper presented the observation results of organic matters concentrations in agricultural runoff from different plant fields (vegetable, flower and rice) in the Red River Delta in 2013 -2014. The results showed that DOC concentrations varied in a high range from 1.0 mg.L-1 to 37.1 mg.L-1, averaging 10.2 ± 6.2 mg.L-1 whereas POC concentrations varied from 0.5 to 4.5 mg.L-1, averaging 1.7 ± 0.7 mg.L-1 for a total 104 samples observed. TOC concentrations in water from the vegetable and flower fields (11.7 ± 7.3 mg.L-1 and 12.6 ± 6.0 mg.L-1 respectively) were higher than the one from the rice field (8.5 ± 6.6 mg.L-1). Lower organic matters concentrations were found in the rainy season than in the dry season due to dilution process. The results suggest the needs for regularly monitoring and efforts to control organic matter pollution from agricultural runoff in the Red River basin or other river basins in developing countries. / Do sử dụng phân bón và thể tích nước tưới lớn, canh tác nông nghiệp đã và đang góp phần đáng kể gây ô nhiễm nguồn nước. Sông Hồng nằm ở Việt Nam, nơi ngành nông nghiệp đóng vai trò quan trọng trong nền kinh tế. Bài báo trình bày kết quả quan trắc hàm lượng cacbon hữu cơ (TOC) bao gồm dạng hòa tan (DOC) và không tan (POC), trong nước chảy tràn từ đất canh tác (rau, hoa, lúa) ở đồng bằng sông Hồng năm 2013 -2014. Kết quả cho thấy DOC thay đổi rất rộng từ 1,0 mg.L-1 đến 37,1 mg.L-1, trung bình đạt 10,2 ± 6,2 mg.L-1 trong khi POC thay đổi từ 0,5 mg. L-1 đến 4,5 mg.L-1, trung bình đạt 1,7 ± 0,7 mg.L-1 đối với 104 mẫu nước. TOC từ trồng rau và hoa (11,7 ± 7,3 mg. L-1 và 12,6 ± 6,0 mg.L-1) cao hơn so với trồng lúa (8,5 ± 6,6 mg. L-1). TOC trong mùa mưa thấp hơn so với mùa khô. Cần thường xuyên giám sát và nỗ lực kiểm soát ô nhiễm chất hữu cơ do nước chảy tràn từ đất canh tác ở lưu vực sông Hồng.

Eine biochemische Indikation des Anteils exogener organischer Kohlenstoffquellen (EOC), der nach dem Eintrag potenziell im Boden verbleibt (Cpot) wurde entwickelt. Haupthypothese dieser Studie war, dass der Abbau von EOC durch die biochemische Zusammensetzung vorhergesagt werden kann, welche bei Pflanzenrückständen von der Kulturart, dem Pflanzenrückstandstyp sowie dem Anbausystem und im Allgemeinen vom Ausgangssubstrat organischer Düngestoffe und der EOC-Kategorie (pyrogen , mikrobiell und pflanzlich) beeinflusst wird. Zunächst wurden Pflanzenrückstände im Energiepflanzenanbau zur Biogasgewinnung (Restpflanze / Stroh, Stoppeln, Grobwurzeln, Feinwurzeln, natürlicher Bestandsabfall) von Mais, Sorghum, Sudangras, Wintergetreide, Hafer, Erbse in Einzel-, Zwei- und Mischkultursystemen betrachtet. In einem zweiten Schritt wurden Pflanzenrückstände im Allgemeinen mit organischen Düngern, Komposten, Rückständen aus anaerober Vergärung in der Biogasproduktion (Gärrückstände) und Biokohlen verglichen. Die biochemische Zusammensetzung von EOC wurde durch die Konzentrationen von Kohlenstoff- (C), Stickstoff (N), wasserlöslicher Kohlehydrate (WSC), Hemizellulose (HEM), Zellulose (CEL) und Lignin (LIC) in g pro kg Trockenmasse dargestellt. In Inkubationsversuchen wurde EOC gleichmäßig mit Boden vermischt und über 310 Tage die Zugabe-induzierte Kohlendioxid-Freisetzung gemessen. Cpot wurde als Grenzwert der Modellschätzung für die Inkubationsdaten bestimmt. Die Beziehung zwischen biochemischer Zusammensetzung und Cpot wurde durch die Partial-Least-Squares-Regression-Methode abgeleitet. Cpot unterschied sich stärker zwischen verschiedenen organischen Düngestoffen, als speziell zwischen verschiedenen Pflanzenrückständen und konnte durch die biochemische Zusammensetzung vorhergesagt werden. Der Indikator für Cpot (in g C pro kg EOC) wurde als Ipot = 269 + 13 N – 0.5 WSC + 0.7 CEL + 1.5 LIC für Pflanzenrückstände und im Allgemeinen als Ipot = 924 – 1.9 C + 2.0 LIC vorgeschlagen. / A biochemical indication for the fraction of exogenous organic carbon (EOC), potentially remaining in soil after application (Cpot) has been developed. Main hypothesis of this study was that decomposition of EOC can be predicted by the biochemical composition, which in case of plant residues is influenced by the crop residue type, crop species and agricultural management and in general depends on the original substrate and category (pyrogen, microbial, and plant-derived EOC) of organic materials. A first set of EOC was created, containing plant residues in energy crop cultivation for biogas production (shoot / straw, stubble, coarse root, fine root, and litter) of maize, sorghum, sudan grass, winter cereal, pea, and oats in single-, double- and intercropping systems. In a second set of EOC, plant residues in general were compared with other organic fertilisers, urban composts, residues of anaerobic fermentation in biogas production (digestates), and biochar. The biochemical composition of EOC was characterised by the concentrations of carbon (C), nitrogen (N), water-soluble carbohydrates (WSC), hemicelluloses (HEM), cellulose (CEL), and lignin (LIC) in g per kg dry matter. In incubation experiments, EOC was homogeneously incorporated into soil and EOC-induced carbon dioxide-release was measured for 310 d. Cpot was determined as modelled limit for the incubation results. Finally, the relation between biochemical composition and Cpot of EOC was evaluated by the partial least squares regression method. Cpot largely varied between different types and categories of EOC, while less variation was obtained between different plant residues. The biochemical composition was predictive for Cpot (expressed as g C per kg EOC), proposing the biochemical indicator as Ipot = 269 + 13 N – 0.5 WSC + 0.7 CEL + 1.5 LIC specifically for plant residues and as Ipot = 924 – 1.9 C + 2.0 LIC for EOC in general.

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We investigated the effects of substrate (cellulose or starch) and different clay contents on the production of microbial extracellular polymeric substances (EPS) and concomitant development of stable soil aggregates. Soils were incubated with different amounts of montmorillonite (+ 0.1%, + 1%, + 10%) both with and without two substrates of contrasting quality (starch and cellulose). Microbial respiration (CO2), biomass carbon (C), EPS-protein, and EPS-polysaccharide were determined over the experimental period. The diversity and compositional shifts of microbial communities (bacteria/archaea) were analysed by sequencing 16S rRNA gene fragments amplified from soil DNA. Soil aggregate size distribution was determined and geometric mean diameter calculated for aggregate formation. Aggregate stabilities were compared among 1–2-mm size fraction. Starch amendment supported a faster increase than cellulose in both respiration and microbial biomass. Microbial community structure and composition differed depending on the C substrate added. However, clay addition had a more pronounced effect on alpha diversity compared to the addition of starch or cellulose. Substrate addition resulted in an increased EPS concentration only if combined with clay addition. At high clay addition, starch resulted in higher EPS concentrations than cellulose. Where additional substrate was not provided, EPS-protein was only weakly correlated with aggregate formation and stability. The relationship became stronger with addition of substrate. Labile organic C thus clearly plays a role in aggregate formation, but increasing clay content was found to enhance aggregate stability and additionally resulted in the development of distinct microbial communities and increased EPS production.