Summary1. Climate change in the subarctic is expected to influence vegetation composition, specifically bryophyte and lichen communities, thereby modifying litter decomposition rates and carbon (C) dynamics of these systems with possible feedbacks to climate. 2. In a 2-year experiment, we investigated decomposition rates and chemical traits of 27 bryophytes, 17 lichens and 5 vascular plants in litter beds in subarctic Sweden. The majority of the sampled cryptogam species are widespread at higher northern latitudes. 3. Average 2-year litter decomposition rates (exponential mass loss constant k) of lichen (0.44 ± 0.01) and vascular plant (0.56 ± 0.03) species were higher than that of bryophytes (0.11 ± 0.01), while within main cryptogam taxa, species identity was an important determinant of mass loss rates. At cryptogam group level, 2-year litter mass loss of Sphagnum was significantly lower than for non-Sphagnum mosses and liverworts. Within lichens, N 2 -fixing versus non-N 2 -fixing lichens showed no variation in decomposability. 4. In a subset of the large species set, mass loss differed both among incubation environments (reflecting nutrient-rich and poor birch forest and Sphagnum peatlands, respectively) and species. The pattern of mass loss across incubation environments was not consistent among cryptogam species. N 2 -fixing, in contrast to non-N 2 -fixing lichens with lower nitrogen (N) levels displayed similar decomposition rates across incubation environments. Mass loss of non-Sphagnum mosses was correlated with initial N irrespective of incubation environment. 5. Litter mass loss of cryptogam taxa could be predicted very well from infrared spectra of the initial chemical composition of the species, by application of Fourier transform infrared using an attenuated total reflectance probe. The initial macronutrient concentrations (N, phosphorus, C and cations) and initial litter pH correlated less well. 6. Synthesis. We showed comprehensively that decomposition rates of bryophytes are generally lower than those of lichens and vascular plants. Among bryophyte or lichen species there is also great variation in litter decomposability which depends strongly on species-specific chemistry. Our data will help predict changing land surface feedback to C cycles and climate in cold biomes by understanding long-term climate effects on litter decomposability through shifting vegetation composition.

In this contribution two ways are described, how it is possible to achieve perfectly cured and processible propellants with prilled ADN, low amounts of HMX 5 μm mps and a binder system based on GAP diole and GAP triole oligomers with and without TMETN as a nitrate ester plasticizer. It was shown how it will be possible to suppress the strongly gas forming reaction between ADN and reactive isocyanates by a mixture of stabilizers. In this way it was possible to create minimum smoke ADN/HMX/GAP/TMETN propellants cured with the triisocyanate N100. In the second part an unconventional binder system based on the 1.3 dipolar cycloaddition reaction of azido groups with acetylene compounds forming 1,2,3‐triazole heterocyclic rings has been applied for ADN/GAP and AP/GAP propellants. Together with small parts of HMX formulations with ADN/HMX/GAP and the corresponding AP/HMX/GAP exhibit high thermodynamic performance, are easily processible, and cure successfully at 60 °C. Their basic properties consisting of burning behavior and mechanical properties, at ambient temperature, chemical stability, and sensitivity have been investigated and are compared to each other.

This work describes the synthesis and the thermoanalytical characterization of guanidinium‐5‐aminotetrazolate (GA). GA is a new nitrogen‐rich energetic material. It is not mentioned in the chemical literature so far. The molecular structure of the compound has been determined by IR, 1H‐, 13C‐ and 15N‐NMR spectroscopy. The thermal properties, the decomposition pathways and its volatile products were investigated by thermal analysis and are discussed.

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A procedure is described for successfully benchmarking different inline spectroscopic techniques in a microreaction plant. The objective was to identify the highest calibration precision for the real-time quantification of the main product. Investigated methods were Raman-, near infrared-, and visible spectroscopy. Besides microreaction technology, the procedure comprises chemometric approaches using statistical experimental design tools and multivariate calibration methods. A calibration model was set up and validated within a defined parameter space (temperature, stoichiometry, and flow rate). The experimental basis was the investigation of toluene nitration using two different nitrating agents. The first reaction was a homogeneous nitration with pure nitric acid as the nitrating agent. It was found that Raman-spectroscopy generates the highest precision. In the second reaction, a heterogeneous liquid-liquid system was obtained using mixed acids. In this case, the precision is very similar for all methods with no preferences for a specific method. As well as investigating the calibration model, additional testing of the observed flow patterns was undertaken for the latter reaction, using the sensitive and very fast AOTF-NIR-spectroscopy.